Publications associated with registered cell lines
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Ergin Ahmet Doğan, Seçen Erhan, Celik Aybuke, Uner Burcu
DQAsomes as a Coenzyme Q10 Delivery Vehicle: A Step Forward Therapy in Leigh Disease
Ergin Ahmet Doğan et al. DQAsomes as a Coenzyme Q10 Delivery Vehicle: A Step Forward Therapy in Leigh Disease. . 2025-03-00. DOI: 10.1007/s12668-024-01714-4 MDCi007-A 2025-03-00 2025-03-00 DOI: 10.1007/s12668-024-01714-4Associated cell lines:
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Lyu Yongkang, Cui Yonglin, Chen Xiaolin, Shen Hao, Xu He, Zhang Changzhe, Meng Qingtian
Mechanics of poly-arginine adsorption onto cell membrane by GM1 and their cluster forming: Coarse-grained molecular dynamics study
Lyu Yongkang et al. Mechanics of poly-arginine adsorption onto cell membrane by GM1 and their cluster forming: Coarse-grained molecular dynamics study. . 2025-02-00. DOI: 10.1016/j.molstruc.2024.140690 CHOCi005-A 2025-02-00 2025-02-00 DOI: 10.1016/j.molstruc.2024.140690Associated cell lines:
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Lee Younsu, Koo Okjae, Saadeldin Islam M.
Generation of induced pluripotent stem cells from the Asian bats
Lee Younsu et al. Generation of induced pluripotent stem cells from the Asian bats. . 2024-12-31. DOI: 10.1080/23144599.2024.2384835 JUCGRMi002-AGWCMCi006-AKMUGMCi010-A 2024-12-31 2024-12-31 DOI: 10.1080/23144599.2024.2384835Associated cell lines:
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Wydrych Agata, Pakuła Barbara, Janikiewicz Justyna, Dobosz Aneta M., Jakubek-Olszewska Patrycja, Skowrońska Marta, Kurkowska-Jastrzębska Iwona, Cwyl Maciej, Popielarz Mariola, Pinton Paolo, Zavan Barbara, Dobrzyń Agnieszka, Lebiedzińska-Arciszewska Magdalena, Więckowski Mariusz R.
Metabolic impairments in neurodegeneration with brain iron accumulation
Wydrych Agata et al. Metabolic impairments in neurodegeneration with brain iron accumulation. . 2025-01-00. DOI: 10.1016/j.bbabio.2024.149517 AKOSi010-A 2025-01-00 2025-01-00 DOI: 10.1016/j.bbabio.2024.149517Associated cell lines:
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Holtes Lara K., de Bruijn Suzanne E., Cremers Frans P.M., Roosing Susanne
Dual inheritance patterns: A spectrum of non-syndromic inherited retinal disease phenotypes with varying molecular mechanisms
Holtes Lara K. et al. Dual inheritance patterns: A spectrum of non-syndromic inherited retinal disease phenotypes with varying molecular mechanisms. . 2025-01-00. DOI: 10.1016/j.preteyeres.2024.101308 NUIGi027-ANUIGi028-ANUIGi029-AUCLi014-AUCLi015-APUMCHi018-A 2025-01-00 2025-01-00 DOI: 10.1016/j.preteyeres.2024.101308Associated cell lines:
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Lv Yafeng, Cui Zhi, Li Hongbo, Wang Jing, Wei Mulan, Hu Yuanlang, Li Xun, Cao Chunyu, Zhang Ye, Wang Wei
Identification of AAV serotypes for gene therapy in Krabbe iPSCs-derived brain organoids
Lv Yafeng et al. Identification of AAV serotypes for gene therapy in Krabbe iPSCs-derived brain organoids. . 2025-01-00. DOI: 10.1016/j.gendis.2024.101269 PUMCi001-A 2025-01-00 2025-01-00 DOI: 10.1016/j.gendis.2024.101269Associated cell lines:
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Lu S, Chen M, Liu X, Li J, Liu H, Li S
Generation of a BEST1 Pr-EGFP reporter human embryonic stem cell line via CRISPR/Cas9 editing
Lu S et al. Generation of a BEST1 Pr-EGFP reporter human embryonic stem cell line via CRISPR/Cas9 editing. . 2024-12-09. Pubmed ID: 39667064; DOI: 10.1016/j.scr.2024.103625 WAe009-AWAe009-A-2CSUe011-A 2024-12-09 2024-12-09 PubMed: 39667064 DOI: 10.1016/j.scr.2024.103625Associated cell lines:
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Bastrich Asya, Antonov Daniil, Podzhilkova Aleksandra, Petrova Darya A., Pylina Svetlana V., Laptev Dmitriy N., Sechko Elena A., Kuznetsov Sergey N., Vetchinkina Ekaterina A., Mokrysheva Natalia G.
Generation of an induced pluripotent stem cell line ERCi003-A derived from a patient with maturity-onset diabetes of the young type 10 caused by a heterozygousINSmutation
Bastrich Asya et al. Generation of an induced pluripotent stem cell line ERCi003-A derived from a patient with maturity-onset diabetes of the young type 10 caused by a heterozygousINSmutation. . 2024-12-05. DOI: 10.1101/2024.12.04.626760 ERCi003-A 2024-12-05 2024-12-05 DOI: 10.1101/2024.12.04.626760Associated cell lines:
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Bastrich Asya, Antonov Daniil, Podzhilkova Aleksandra, Petrova Darya A., Pylina Svetlana V., Laptev Dmitriy N., Sechko Elena A., Kuznetsov Sergey N., Vetchinkina Ekaterina A., Mokrysheva Natalia G.
Generation of iPSC line ERCi004-A from human dermal fibroblasts of a patient with maturity-onset diabetes of the young type 3 caused by a heterozygous mutation in theHNF1Agene
Bastrich Asya et al. Generation of iPSC line ERCi004-A from human dermal fibroblasts of a patient with maturity-onset diabetes of the young type 3 caused by a heterozygous mutation in theHNF1Agene. . 2024-12-05. DOI: 10.1101/2024.12.04.626820 ERCi004-A 2024-12-05 2024-12-05 DOI: 10.1101/2024.12.04.626820Associated cell lines:
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Nitaramorn N, Kobpornchai P, Tongkrajang N, Chaisri U, Imwong M, Kulkeaw K
Human liver organoids are susceptible to Plasmodium vivax infection
Nitaramorn N et al. Human liver organoids are susceptible to Plasmodium vivax infection. . 2024-12-05. Pubmed ID: 39639330; DOI: 10.1186/s12936-024-05202-8; PMC: PMC11622667 MUSIi001-A 2024-12-05 2024-12-05 PubMed: 39639330 DOI: 10.1186/s12936-024-05202-8Associated cell lines:
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Nayak D, Shivakumar S, Shetty R, Prashanthi KN, Ghosh A, Jeyabalan N, Chakrabarty K
Trehalose extricates impaired mitochondrial and autophagy dysregulation in patient iPSC-derived macular corneal dystrophy disease model
Nayak D et al. Trehalose extricates impaired mitochondrial and autophagy dysregulation in patient iPSC-derived macular corneal dystrophy disease model. . 2024-12-05. Pubmed ID: 39639354; DOI: 10.1186/s13287-024-04016-4; PMC: PMC11622490 GLNNFi001-A 2024-12-05 2024-12-05 PubMed: 39639354 DOI: 10.1186/s13287-024-04016-4Associated cell lines:
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Bekhite MM, Hübner S, Kretzschmar T, Backsch C, Weise A, Klein E, Bogoviku J, Westphal J, Schulze PC
Generation of a human induced pluripotent stem cell lines (UKJi003-A) from a patient with Fabry disease and healthy donor (UKJi004-A)
Bekhite MM et al. Generation of a human induced pluripotent stem cell lines (UKJi003-A) from a patient with Fabry disease and healthy donor (UKJi004-A). . 2024-12-03. Pubmed ID: 39701018; DOI: 10.1016/j.scr.2024.103620 UKJi003-AUKJi004-A 2024-12-03 2024-12-03 PubMed: 39701018 DOI: 10.1016/j.scr.2024.103620 -
Zhang D, Huang D, Larcher LM, Zaw K, Chen SC, Jennings L, Lamey TM, Thompson JA, McLaren TL, Chen FK, McLenachan S
Derivation of two induced pluripotent stem cell lines from a healthy control subject
Zhang D et al. Derivation of two induced pluripotent stem cell lines from a healthy control subject. . 2024-12-03. Pubmed ID: 39642595; DOI: 10.1016/j.scr.2024.103621 LEIi019-ALEIi021-ALEIi021-B 2024-12-03 2024-12-03 PubMed: 39642595 DOI: 10.1016/j.scr.2024.103621 -
Baiocco Paola, Barolo Lorenzo, Mautone Lorenza, Gigante Ylenia, Ghirga Silvia, Mura Francesco, Farina Maria Vittoria, Tacconi Stefano, Dini Luciana, Ruocco Giancarlo, Boffi Alberto, Milanetti Edoardo, Angelantonio Silvia Di
Short-Chain Polyphosphates Induce Tau Fibrillation and Neurotoxicity in Human iPSC-Derived Retinal Neurons
Baiocco Paola et al. Short-Chain Polyphosphates Induce Tau Fibrillation and Neurotoxicity in Human iPSC-Derived Retinal Neurons. . 2024-12-02. DOI: 10.21203/rs.3.rs-5409787/v1 SIGi001-A 2024-12-02 2024-12-02 DOI: 10.21203/rs.3.rs-5409787/v1Associated cell lines:
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Xin H, Li Y, Zhang K, Ji A, Fan M
Generation of an induced pluripotent stem cell line from a type 1 neurofibromatosis patient with NF1 mutation
Xin H et al. Generation of an induced pluripotent stem cell line from a type 1 neurofibromatosis patient with NF1 mutation. . 2024-12-00. Pubmed ID: 39332134; DOI: 10.1016/j.scr.2024.103568 JNCHi001-A 2024-12-00 2024-12-00 PubMed: 39332134 DOI: 10.1016/j.scr.2024.103568Associated cell lines:
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Sun X, Mao S, Liang Y, Duan C, Cui Z, Gu J, Jiang B, Ding C, Chen J, Tang S
Introduction of an RS1 mutation causative variant consistent with identified XLRS patient using CRISPR/Cas9 technology in normal iPSC
Sun X et al. Introduction of an RS1 mutation causative variant consistent with identified XLRS patient using CRISPR/Cas9 technology in normal iPSC. . 2024-12-00. Pubmed ID: 39232357; DOI: 10.1016/j.scr.2024.103549 CSUASOi001-ACSUi007-A 2024-12-00 2024-12-00 PubMed: 39232357 DOI: 10.1016/j.scr.2024.103549Associated cell lines:
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Rha AK, Christensen CL, Kan SH, Harb JF, Andrade-Heckman P, Wang RY
Generation of an infantile GM1 gangliosidosis induced pluripotent stem cell line (CHOCi005-A) for disease modeling and therapeutic testing
Rha AK et al. Generation of an infantile GM1 gangliosidosis induced pluripotent stem cell line (CHOCi005-A) for disease modeling and therapeutic testing. . 2024-12-00. Pubmed ID: 39303321; DOI: 10.1016/j.scr.2024.103552 CHOCi005-A 2024-12-00 2024-12-00 PubMed: 39303321 DOI: 10.1016/j.scr.2024.103552Associated cell lines:
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Liu R, Weng G, Zheng F, Chen J, Wang K, Han J, Huang J, Yan L, Jin J
Generation of an integration-free induced pluripotent stem cell line, FJMAi001-A, from a Marfan syndrome patient with a heterozygous mutation c.2777G > A (p.Cys926Tyr) in FBN1
Liu R et al. Generation of an integration-free induced pluripotent stem cell line, FJMAi001-A, from a Marfan syndrome patient with a heterozygous mutation c.2777G > A (p.Cys926Tyr) in FBN1. . 2024-12-00. Pubmed ID: 39515109; DOI: 10.1016/j.scr.2024.103591 FJMAi001-A 2024-12-00 2024-12-00 PubMed: 39515109 DOI: 10.1016/j.scr.2024.103591Associated cell lines:
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Rodriguez-Lopez A, Huang X, Chen C, Zou J, Zheng W, Chen G
Generation of an induced pluripotent stem cell line (TRNDi042-A) from a Mucopolysaccharidosis type IIIB patient with homozygous p. R626X (c. 1876C > T) mutation in the NAGLU gene
Rodriguez-Lopez A et al. Generation of an induced pluripotent stem cell line (TRNDi042-A) from a Mucopolysaccharidosis type IIIB patient with homozygous p. R626X (c. 1876C > T) mutation in the NAGLU gene. . 2024-12-00. Pubmed ID: 39579553; DOI: 10.1016/j.scr.2024.103612 TRNDi042-A 2024-12-00 2024-12-00 PubMed: 39579553 DOI: 10.1016/j.scr.2024.103612Associated cell lines:
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Liu D, Shen J, Yang Z, Fan H, Wang H, Liang P, Gong T
Generation of a lamin A/C knockout human induced pluripotent stem cell line (ZJULLi007-A) via CRISPR/Cas9
Liu D et al. Generation of a lamin A/C knockout human induced pluripotent stem cell line (ZJULLi007-A) via CRISPR/Cas9. . 2024-12-00. Pubmed ID: 39427442; DOI: 10.1016/j.scr.2024.103579 ZJULLi007-A 2024-12-00 2024-12-00 PubMed: 39427442 DOI: 10.1016/j.scr.2024.103579Associated cell lines:
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Cheng J, Zhai Y, Guo X, Wang X, Ma M, Ren X, Wang S, Cui H, Ren Q
Generation of an induced pluripotent stem cell line (HMSCATi004-A) from an early onset Parkinson's disease patient with PRKN gene mutation
Cheng J et al. Generation of an induced pluripotent stem cell line (HMSCATi004-A) from an early onset Parkinson's disease patient with PRKN gene mutation. . 2024-12-00. Pubmed ID: 39405989; DOI: 10.1016/j.scr.2024.103578 HMSCATi004-A 2024-12-00 2024-12-00 PubMed: 39405989 DOI: 10.1016/j.scr.2024.103578Associated cell lines:
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Jyoti Saikia B, Bhardwaj J, Saini A, Rajan R, B K B
Generation of an induced pluripotent stem cell (iPSC) line (IGIBi026-A) derived from Wilson disease patient harboring compound heterozygous mutations [c.2165dupT (p.R723Efs31) and c.C813A (p.C271*)] in the ATP7B gene
Jyoti Saikia B et al. Generation of an induced pluripotent stem cell (iPSC) line (IGIBi026-A) derived from Wilson disease patient harboring compound heterozygous mutations [c.2165dupT (p.R723Efs31) and c.C813A (p.C271*)] in the ATP7B gene. . 2024-12-00. Pubmed ID: 39326255; DOI: 10.1016/j.scr.2024.103567 IGIBi026-A 2024-12-00 2024-12-00 PubMed: 39326255 DOI: 10.1016/j.scr.2024.103567Associated cell lines:
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Jiang X, Liu Q, Yang L, Zhang X, Gao J, Jiang Y
Generation of a MYH6 (c.4034T > C) mutant human embryonic stem cell line via CRISPR base editing
Jiang X et al. Generation of a MYH6 (c.4034T > C) mutant human embryonic stem cell line via CRISPR base editing. . 2024-12-00. Pubmed ID: 39541768; DOI: 10.1016/j.scr.2024.103610 WAe009-AWAe009-A-1D 2024-12-00 2024-12-00 PubMed: 39541768 DOI: 10.1016/j.scr.2024.103610Associated cell lines:
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Tohari M, Sanjaya R, Yuliana Sari S, Tedjobagaskara B, Ibnu Faisal A, Alvin Prawira M, Oktaviani Dwi Putri A, Faza N, Murti H, Widyastuti HP
Generation of footprint-free human induced pluripotent stem cell line (SCIKFi001-B) from cGMP grade umbilical cord-derived mesenchymal stem cells (UC-MSCs) using episomal-plasmid based reprogramming approach
Tohari M et al. Generation of footprint-free human induced pluripotent stem cell line (SCIKFi001-B) from cGMP grade umbilical cord-derived mesenchymal stem cells (UC-MSCs) using episomal-plasmid based reprogramming approach. . 2024-12-00. Pubmed ID: 39332133; DOI: 10.1016/j.scr.2024.103566 SCIKFi001-B 2024-12-00 2024-12-00 PubMed: 39332133 DOI: 10.1016/j.scr.2024.103566Associated cell lines:
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Woo Lim S, In Lee K, Cui S, Fang X, Jin Shin Y, Lee H, Woo Yang C, Young Lee J, Ha Chung B
Generation of a human SLC12A3 knock-in human induced pluripotent stem cell line (CMCi014-A-82) using CRISPR-Cas9 system
Woo Lim S et al. Generation of a human SLC12A3 knock-in human induced pluripotent stem cell line (CMCi014-A-82) using CRISPR-Cas9 system. . 2024-12-00. Pubmed ID: 39163808; DOI: 10.1016/j.scr.2024.103522 UCSFi001-A-82 2024-12-00 2024-12-00 PubMed: 39163808 DOI: 10.1016/j.scr.2024.103522Associated cell lines:
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Mizuno-Iijima S, Kawamoto S, Asano M, Mashimo T, Wakana S, Nakamura K, Nishijima KI, Okamoto H, Saito K, Yoshina S, Miwa Y, Nakamura Y, Ohkuma M, Yoshiki A
Mammalian genome research resources available from the National BioResource Project in Japan
Mizuno-Iijima S et al. Mammalian genome research resources available from the National BioResource Project in Japan. . 2024-12-00. Pubmed ID: 39261329; DOI: 10.1007/s00335-024-10063-2; PMC: PMC11522087 BRCi001-ABRCi004-ABRCi005-A 2024-12-00 2024-12-00 PubMed: 39261329 DOI: 10.1007/s00335-024-10063-2 -
Sleiman Y, Reisqs JB, Bianca Tan R, Cecchin F, Chahine M, Boutjdir M
Generation of an iPSC cell line (VANYHHi001-A) from a patient with cardiac arrythmias carrying CACNA1D, SCN5A, and DSP variants
Sleiman Y et al. Generation of an iPSC cell line (VANYHHi001-A) from a patient with cardiac arrythmias carrying CACNA1D, SCN5A, and DSP variants. . 2024-12-00. Pubmed ID: 39551029; DOI: 10.1016/j.scr.2024.103608 CBRCULi001-ACBRCULi002-ACBRCULi003-ACBRCULi004-ACBRCULi005-ACBRCULi006-ACBRCULi007-ACBRCULi016-ACBRCULi017-ACBRCULi016-A-1VANYHHi001-A 2024-12-00 2024-12-00 PubMed: 39551029 DOI: 10.1016/j.scr.2024.103608 -
Sun T, Chen B, Zhang D, Xu X, Gao J, Sun J, Wei M
Generation of hereditary spastic paraplegia patient-derived induced pluripotent stem cell line UJSi003-A
Sun T et al. Generation of hereditary spastic paraplegia patient-derived induced pluripotent stem cell line UJSi003-A. . 2024-12-00. Pubmed ID: 39154415; DOI: 10.1016/j.scr.2024.103535 UJSi001-AUJSi002-AUJSi003-A 2024-12-00 2024-12-00 PubMed: 39154415 DOI: 10.1016/j.scr.2024.103535 -
Boen HM, Vandendriessche B, Schippers J, Rabaut L, Nijak-Paeske A, Ponsaerts P, Van Craenenbroeck EM, Loeys B, Alaerts M
Generation of four distinct isogenic cell lines with truncating variants in I-band or A-band titin
Boen HM et al. Generation of four distinct isogenic cell lines with truncating variants in I-band or A-band titin. . 2024-12-00. Pubmed ID: 39167847; DOI: 10.1016/j.scr.2024.103536 BBANTWi012-ABBANTWi012-A-1BBANTWi012-A-2BBANTWi012-A-3BBANTWi012-A-4 2024-12-00 2024-12-00 PubMed: 39167847 DOI: 10.1016/j.scr.2024.103536Associated cell lines:
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Africano Chiara, Bachetti Tiziana, Uva Paolo, Pitollat Gabriel, Del Zotto Genny, Giacopelli Francesca, Recchi Giada, Lenfant Nicolas, Madani Amélia, Beckouche Nathan, Thoby-Brisson Muriel, Ceccherini Isabella
Identification of a histone deacetylase inhibitor as a therapeutic candidate for congenital central hypoventilation syndrome
Africano Chiara et al. Identification of a histone deacetylase inhibitor as a therapeutic candidate for congenital central hypoventilation syndrome. . 2024-12-00. DOI: 10.1016/j.omtn.2024.102319 BGUi004-ABGUi005-AUMILi027-AUMILi028-A 2024-12-00 2024-12-00 DOI: 10.1016/j.omtn.2024.102319Associated cell lines:
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Jiao K, Zhang J, Wang N, Gu X, Chang X, Xia X, Zhu B, Gao M, Cheng N, Zhao C, Xi J, Zhu W
Human induced pluripotent stem cell line (FDHSi005-A) derived from a patient with a deep intronic variant in the GNE gene
Jiao K et al. Human induced pluripotent stem cell line (FDHSi005-A) derived from a patient with a deep intronic variant in the GNE gene. . 2024-12-00. Pubmed ID: 39303320; DOI: 10.1016/j.scr.2024.103562 FDHSi005-A 2024-12-00 2024-12-00 PubMed: 39303320 DOI: 10.1016/j.scr.2024.103562Associated cell lines:
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Wang Yanli, Liu Zengping, Li Yong, Nie Zhipeng, Xu Baicheng, Zhu Yiming, Duan Shihong, Chen Xingjian, Tan Huan, Dang Jiong, Guan Minxin, Guo Yufen
A Novel Mutation Located in the N‐Terminal Domain of
Wang Yanli et al. A Novel Mutation Located in the N‐Terminal Domain ofMYO15A Caused Sensorineural Hearing LossMYO15A Caused Sensorineural Hearing Loss. . 2024-12-00. DOI: 10.1002/mgg3.70042 CSUXHi004-A 2024-12-00 2024-12-00 DOI: 10.1002/mgg3.70042Associated cell lines:
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Boullé M, Leleu A, Schacre S, Banal C, Boucharlat A, Renault S, Hollenstein M, Frosk P, Yates F, Lefort N, Agou F
Generation of IPi002-A/B/C human induced pluripotent stem cell lines from MARCH amniotic fluid cells
Boullé M et al. Generation of IPi002-A/B/C human induced pluripotent stem cell lines from MARCH amniotic fluid cells. . 2024-12-00. Pubmed ID: 39447316; DOI: 10.1016/j.scr.2024.103589 IPi001-AIPi002-A 2024-12-00 2024-12-00 PubMed: 39447316 DOI: 10.1016/j.scr.2024.103589 -
Okumura H, Hayashi Y, Arioka Y, Kushima I, Mori D, Ozaki N
Generation of induced pluripotent stem cells from a schizophrenia patient with heterozygous 1q21.1 deletion
Okumura H et al. Generation of induced pluripotent stem cells from a schizophrenia patient with heterozygous 1q21.1 deletion. . 2024-12-00. Pubmed ID: 39288675; DOI: 10.1016/j.scr.2024.103555 PNUi004-APNUi004-BPNUi004-C 2024-12-00 2024-12-00 PubMed: 39288675 DOI: 10.1016/j.scr.2024.103555 -
Erliandri I, Sangotra A, Keller L, Lieberman AP, Smith GD
A spinal and bulbar muscular atrophy (SBMA) disease-specific human embryonic stem cell (hESC) line, UMICHe002-A/UM197-1
Erliandri I et al. A spinal and bulbar muscular atrophy (SBMA) disease-specific human embryonic stem cell (hESC) line, UMICHe002-A/UM197-1. . 2024-12-00. Pubmed ID: 39353357; DOI: 10.1016/j.scr.2024.103548 UMICHe001-AUMICHe002-A 2024-12-00 2024-12-00 PubMed: 39353357 DOI: 10.1016/j.scr.2024.103548Associated cell lines:
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Arunachal G, Nimonkar MM, Mahadeva P, Sukrutha R, Raghavendra K, Chetan GK, Venkataswamy MM, Mehta B, Markandeya YS
Generation of induced pluripotent stem cell line, NIMHi013-A, from PBMCs of a female child with epilepsy carrying a novel SCN1A variant
Arunachal G et al. Generation of induced pluripotent stem cell line, NIMHi013-A, from PBMCs of a female child with epilepsy carrying a novel SCN1A variant. . 2024-12-00. Pubmed ID: 39383605; DOI: 10.1016/j.scr.2024.103573 NIMHi007-ANIMHi009-ALVPEIi004-ANIMHi013-ALVPEIi005-ALVPEIi007-BLVPEIi008-B 2024-12-00 2024-12-00 PubMed: 39383605 DOI: 10.1016/j.scr.2024.103573Associated cell lines:
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Cheng Y, Sun H, Chen X, Li X, Xu Y, Wang Y
Generation of induced pluripotent stem cell line (ZZUi037-A) from a patient with spinocerebellar ataxia type 3
Cheng Y et al. Generation of induced pluripotent stem cell line (ZZUi037-A) from a patient with spinocerebellar ataxia type 3. . 2024-12-00. Pubmed ID: 39603094; DOI: 10.1016/j.scr.2024.103617 ZZUi005-AZZUi037-A 2024-12-00 2024-12-00 PubMed: 39603094 DOI: 10.1016/j.scr.2024.103617 -
Li Y, Du M, Jin Z
Generation of ID1/3 knockout human embryonic stem cell lines (WAe009-A-2A and WAe009-A-2B) derived from H9 using CRISPR/Cas9
Li Y et al. Generation of ID1/3 knockout human embryonic stem cell lines (WAe009-A-2A and WAe009-A-2B) derived from H9 using CRISPR/Cas9. . 2024-12-00. Pubmed ID: 39342788; DOI: 10.1016/j.scr.2024.103569 WAe009-AWAe009-A-2AWAe009-A-2B 2024-12-00 2024-12-00 PubMed: 39342788 DOI: 10.1016/j.scr.2024.103569Associated cell lines:
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Krogulec E, Dobosz AM, Liszewska E, Majchrowicz L, Dobrzyń A
Generation of four human induced pluripotent stem cell lines derived from patients with MPAN, subtype of NBIA, carrying the c.204_214del11 mutation in the C19orf12 gene
Krogulec E et al. Generation of four human induced pluripotent stem cell lines derived from patients with MPAN, subtype of NBIA, carrying the c.204_214del11 mutation in the C19orf12 gene. . 2024-12-00. Pubmed ID: 39489009; DOI: 10.1016/j.scr.2024.103603 IIMCBi001-AIIMCBi002-ANENCKIi001-ANENCKIi002-ANENCKIi003-ANENCKIi004-A 2024-12-00 2024-12-00 PubMed: 39489009 DOI: 10.1016/j.scr.2024.103603Associated cell lines:
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Gubinelli Francesco, Salazar Jose M., Kaspar Janina, Ortiz Irene Santisteban, Schafer Simon T., Burbulla Lena F.
Translational View on Therapeutic Strategies and Upcoming Issues: Stem Cell and Brain Organoid Approaches for Parkinson’s Disease Therapy
Gubinelli Francesco et al. Translational View on Therapeutic Strategies and Upcoming Issues: Stem Cell and Brain Organoid Approaches for Parkinson’s Disease Therapy. . 2025-00-00. DOI: 10.1007/978-1-0716-4083-8_17 RCe015-A 2025-00-00 2025-00-00 DOI: 10.1007/978-1-0716-4083-8_17Associated cell lines:
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Aalders J, Léger L, Hassannia B, Goossens V, Vanden Berghe T, van Hengel J
Improving cardiac differentiation of human pluripotent stem cells by targeting ferroptosis
Aalders J et al. Improving cardiac differentiation of human pluripotent stem cells by targeting ferroptosis. . 2024-12-00. Pubmed ID: 38496011; DOI: 10.1016/j.reth.2024.02.007; PMC: PMC10940893 UGENTi001-AUGENTi001-A-1 2024-12-00 2024-12-00 PubMed: 38496011 DOI: 10.1016/j.reth.2024.02.007Associated cell lines:
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Wang Jinling, Ye Di, Li Shuangpeng, Lu Xuan, Chi Yue, Tang Chengcheng, Zhou Xiaoqing, Chen Min, Zheng Yunwen, Ge Jianyun, Zou Qingjian
Generation of human induced pluripotent stem cells carrying albumin-sfGFP reporter
Wang Jinling et al. Generation of human induced pluripotent stem cells carrying albumin-sfGFP reporter. . 2024-12-00. DOI: 10.1016/j.scr.2024.103543 WYUi003-A 2024-12-00 2024-12-00 DOI: 10.1016/j.scr.2024.103543Associated cell lines:
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Bekhite MM, Hübner S, Kretzschmar T, Backsch C, Weise A, Klein E, Bogoviku J, Westphal J, Christian Schulze P
Generation of human induced pluripotent stem cell lines UKJi001-A and UKJi006-A from patients with heterozygous mutation in the PKP2 gene
Bekhite MM et al. Generation of human induced pluripotent stem cell lines UKJi001-A and UKJi006-A from patients with heterozygous mutation in the PKP2 gene. . 2024-12-00. Pubmed ID: 39332132; DOI: 10.1016/j.scr.2024.103565 UKJi001-AUKJi006-A 2024-12-00 2024-12-00 PubMed: 39332132 DOI: 10.1016/j.scr.2024.103565 -
Wongkidakarn S, Yodtup C, Jantapalaboon D, Phairoh P, Suparak S, Dhepakson P, Tubsuwan A, Bumroongthai K
Generation of human induced pluripotent stem cell (DMSCi001-A) line from hematopoietic stem cells of a healthy female donor
Wongkidakarn S et al. Generation of human induced pluripotent stem cell (DMSCi001-A) line from hematopoietic stem cells of a healthy female donor. . 2024-12-00. Pubmed ID: 39504763; DOI: 10.1016/j.scr.2024.103605 DMSCi001-A 2024-12-00 2024-12-00 PubMed: 39504763 DOI: 10.1016/j.scr.2024.103605Associated cell lines:
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Léger L, Aalders J, Heymans N, Van Acker-Verberckt K, De Bleeckere L, Coucke P, Menten B, Bauce B, Vitiello L, Rampazzo A, Calore M, van Hengel J
Generation of a human induced pluripotent stem cell line UGENTi002-A from an arrhythmogenic cardiomyopathy patient carrying the c.817C>T DSP heterozygous variant and isogenic control using CRISPR/Cas9 editing
Léger L et al. Generation of a human induced pluripotent stem cell line UGENTi002-A from an arrhythmogenic cardiomyopathy patient carrying the c.817C>T DSP heterozygous variant and isogenic control using CRISPR/Cas9 editing. . 2024-12-00. Pubmed ID: 39217685; DOI: 10.1016/j.scr.2024.103537 UGENTi002-AUGENTi002-A-1 2024-12-00 2024-12-00 PubMed: 39217685 DOI: 10.1016/j.scr.2024.103537Associated cell lines:
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Ruotolo G, D'Anzi A, Giovenale AMG, Giacometti C, Ferrari D, Vulcano E, D'Asdia C, Lattante S, Sabatelli M, Codazzi F, Consalez G, Marano M, Di Lazzaro V, Pennuto M, Vescovi A, Rosati J
Induced pluripotent stem cell production (CSSi019-A)(14432) from an asymptomatic subject carrying a expansion of C9orf72 gene
Ruotolo G et al. Induced pluripotent stem cell production (CSSi019-A)(14432) from an asymptomatic subject carrying a expansion of C9orf72 gene. . 2024-12-00. Pubmed ID: 39191178; DOI: 10.1016/j.scr.2024.103540 CSSi017-ACSSi019-A 2024-12-00 2024-12-00 PubMed: 39191178 DOI: 10.1016/j.scr.2024.103540 -
Tanzer K, Meier B, Vulinovic F, Pawlack H, Klein C, Seibler P, Rakovic A
Generation of four human-derived iPSC TorsinA-3xFLAG reporter lines from a DYT-TOR1A patient
Tanzer K et al. Generation of four human-derived iPSC TorsinA-3xFLAG reporter lines from a DYT-TOR1A patient. . 2024-12-00. Pubmed ID: 39490211; DOI: 10.1016/j.scr.2024.103595 LUEi020-ALUEi020-A-1LUEi020-A-2LUEi020-A-3LUEi020-A-4 2024-12-00 2024-12-00 PubMed: 39490211 DOI: 10.1016/j.scr.2024.103595Associated cell lines:
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Hua C, Sun W, Zhang C, Tian X, Qin X, Dong J, Li X
Generation of a human induced pluripotent stem cell line ZZUNEUi030-A from a female patient carrying a heterozygous CALM2 (c.395 A > T) mutation
Hua C et al. Generation of a human induced pluripotent stem cell line ZZUNEUi030-A from a female patient carrying a heterozygous CALM2 (c.395 A > T) mutation. . 2024-12-00. Pubmed ID: 39137556; DOI: 10.1016/j.scr.2024.103515 ZZUNEUi030-A 2024-12-00 2024-12-00 PubMed: 39137556 DOI: 10.1016/j.scr.2024.103515Associated cell lines:
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Giraldo-Berrio Daniela, Jimenez-Del-Rio Marlene, Velez-Pardo Carlos
Minocycline mitigates Aβ and TAU pathology, neuronal dysfunction, and death in the PSEN1 E280A cholinergic-like neurons model of familial Alzheimer’s disease
Giraldo-Berrio Daniela et al. Minocycline mitigates Aβ and TAU pathology, neuronal dysfunction, and death in the PSEN1 E280A cholinergic-like neurons model of familial Alzheimer’s disease. . 2024-12-00. DOI: 10.1016/j.neuropharm.2024.110152 IMEDEAi006-A 2024-12-00 2024-12-00 DOI: 10.1016/j.neuropharm.2024.110152Associated cell lines:
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Uno Narumi, Miyamoto Hitomaru, Yamazaki Kyotaro, Egawa Masaya, Kobayashi Hiroaki, Kazuki Kanako, Osaki Mitsuhiko, Suzuki Teruhiko, Hamamichi Shusei, Oshimura Mitsuo, Tomizuka Kazuma, Kazuki Yasuhiro
Microcell-mediated chromosome transfer between non-identical human iPSCs
Uno Narumi et al. Microcell-mediated chromosome transfer between non-identical human iPSCs. . 2024-12-00. DOI: 10.1016/j.omtn.2024.102382 GZHMUi001-A 2024-12-00 2024-12-00 DOI: 10.1016/j.omtn.2024.102382Associated cell lines:
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A Ababneh N, Barham R, Al-Kurdi B, Al Hadidi S, Ali D, Abdulelah AA, Madadha A, Masri A, Awidi A
Establishment of a human induced pluripotent stem cell (iPSC) line (JUCTCi018-A) from a patient with Charcot-Marie-Tooth disease type 2EE (CMT2EE) due to a homozygous c.122G > A p.(Arg41Gln) mutation in the MPV17 gene
A Ababneh N et al. Establishment of a human induced pluripotent stem cell (iPSC) line (JUCTCi018-A) from a patient with Charcot-Marie-Tooth disease type 2EE (CMT2EE) due to a homozygous c.122G > A p.(Arg41Gln) mutation in the MPV17 gene. . 2024-12-00. Pubmed ID: 39461114; DOI: 10.1016/j.scr.2024.103602 JUCTCi002-AJUCTCi010-AJUCTCi011-AJUCTCi018-A 2024-12-00 2024-12-00 PubMed: 39461114 DOI: 10.1016/j.scr.2024.103602Associated cell lines:
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Jiang M, Long Y, Liu Y, Li R, Xu J, Chi T, Sun M, Li M, Yu H, Yu L, Han X
Establishment of an induced pluripotent stem cell (iPSC) line (JNMUi002-A) from a male patient with schizophrenia
Jiang M et al. Establishment of an induced pluripotent stem cell (iPSC) line (JNMUi002-A) from a male patient with schizophrenia. . 2024-12-00. Pubmed ID: 39368271; DOI: 10.1016/j.scr.2024.103570 JNMUi002-A 2024-12-00 2024-12-00 PubMed: 39368271 DOI: 10.1016/j.scr.2024.103570Associated cell lines:
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Xu X, Wang W, Liu Y, Bäckemo J, Heuchel M, Wang W, Nie Y, Iqbal I, Kratz K, Lendlein A, Ma N
Substrates mimicking the blastocyst geometry revert pluripotent stem cell to naivety
Xu X et al. Substrates mimicking the blastocyst geometry revert pluripotent stem cell to naivety. . 2024-12-00. Pubmed ID: 39134648; DOI: 10.1038/s41563-024-01971-4; PMC: PMC11599042 BIHi001-A 2024-12-00 2024-12-00 PubMed: 39134648 DOI: 10.1038/s41563-024-01971-4Associated cell lines:
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Esteves F, Brito D, Rajado AT, Silva N, Apolónio J, Roberto VP, ALFA Score Consortium, Andrade RP, Calado S, Faleiro ML, Matos C, Marques N, Marreiros A, Nzwalo H, Pais S, Palmeirim I, Simãoa S, Joaquim N, Miranda R, Pêgas A, Raposo DM, Sardo A, Araújo I, Nóbrega C, Castelo-Branco P, Bragança J
Establishment of an induced pluripotent cell line (ABCRIi001-A) from an elderly female for ageing research
Esteves F et al. Establishment of an induced pluripotent cell line (ABCRIi001-A) from an elderly female for ageing research. . 2024-12-00. Pubmed ID: 39437566; DOI: 10.1016/j.scr.2024.103576 ABCRIi001-A 2024-12-00 2024-12-00 PubMed: 39437566 DOI: 10.1016/j.scr.2024.103576Associated cell lines:
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Su S, Ren Y, Zhang H, Liu Y, Liu Y, Li Z, Zhang T, Fang F
Establishment of a transgene-free iPS cell line (SDCHi002-A) from a young patient bearing a NPRL3 mutation and suffering from Epilepsy
Su S et al. Establishment of a transgene-free iPS cell line (SDCHi002-A) from a young patient bearing a NPRL3 mutation and suffering from Epilepsy. . 2024-12-00. Pubmed ID: 39426047; DOI: 10.1016/j.scr.2024.103574 SDCHi002-A 2024-12-00 2024-12-00 PubMed: 39426047 DOI: 10.1016/j.scr.2024.103574Associated cell lines:
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Li Z, Li Z, Lv Y, Gao M, Liu N, Gai Z, Liu Q
Establishment of a non-integrated iPS cell line (SDQLCHi072-A) from a patient suffered from AUTS2 syndrome
Li Z et al. Establishment of a non-integrated iPS cell line (SDQLCHi072-A) from a patient suffered from AUTS2 syndrome. . 2024-12-00. Pubmed ID: 39276529; DOI: 10.1016/j.scr.2024.103554 SDQLCHi072-A 2024-12-00 2024-12-00 PubMed: 39276529 DOI: 10.1016/j.scr.2024.103554Associated cell lines:
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Verma S, Dalabehera S, Maurya R, Singh D, Prasher B, Pandey R, Bapat S, Ramalingam S, Sachidanandan C
Corrigendum to "Generation of an induced pluripotent stem cell line IGIBi18-A from an Indian patient with rubinstein taybi syndrome" [Stem Cell Res. 78 (2024) 103456]
Verma S et al. Corrigendum to "Generation of an induced pluripotent stem cell line IGIBi18-A from an Indian patient with rubinstein taybi syndrome" [Stem Cell Res. 78 (2024) 103456]. . 2024-12-00. Pubmed ID: 39179505; DOI: 10.1016/j.scr.2024.103539 IGIBi018-A 2024-12-00 2024-12-00 PubMed: 39179505 DOI: 10.1016/j.scr.2024.103539Associated cell lines:
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Li Y, Du M, Jin Z
Corrigendum to "Generation of ID1/3 knockout human embryonic stem cell lines (WAe009-A-2A and WAe009-A-2B) derived from H9 using CRISPR/Cas9" [Stem Cell Research 81 (2024) 103569]
Li Y et al. Corrigendum to "Generation of ID1/3 knockout human embryonic stem cell lines (WAe009-A-2A and WAe009-A-2B) derived from H9 using CRISPR/Cas9" [Stem Cell Research 81 (2024) 103569]. . 2024-12-00. Pubmed ID: 39648091; DOI: 10.1016/j.scr.2024.103622 WAe009-AWAe009-A-2AWAe009-A-2B 2024-12-00 2024-12-00 PubMed: 39648091 DOI: 10.1016/j.scr.2024.103622Associated cell lines:
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Mun D, Kang JY, Park M, Yoo G, Kim H, Yun N, Mi Hwang Y, Joung B
Establishment of a human-induced pluripotent stem cell line from a long QT syndrome type 2 patient harboring a KCNH2 mutation
Mun D et al. Establishment of a human-induced pluripotent stem cell line from a long QT syndrome type 2 patient harboring a KCNH2 mutation. . 2024-12-00. Pubmed ID: 39454535; DOI: 10.1016/j.scr.2024.103592 YUCMi022-A 2024-12-00 2024-12-00 PubMed: 39454535 DOI: 10.1016/j.scr.2024.103592Associated cell lines:
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Zhang S, Li J, Pan W, Ren Q, Zhou Y, Chen M, Qu J, Li S
Establishment of a CPAMD8-GFP reporter human embryonic stem cell line, IBBDe001-B, using CRISPR/Cas9 editing
Zhang S et al. Establishment of a CPAMD8-GFP reporter human embryonic stem cell line, IBBDe001-B, using CRISPR/Cas9 editing. . 2024-12-00. Pubmed ID: 39603092; DOI: 10.1016/j.scr.2024.103615 MUSIi001-ACSUe011-AMUSIi001-A-2IBBDe001-B 2024-12-00 2024-12-00 PubMed: 39603092 DOI: 10.1016/j.scr.2024.103615Associated cell lines:
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Wang S, Zeng Q, Chen M, Zhang H, Lv X
Establishment of an induced pluripotent stem cell line (SDCHi011-A) from a healthy Chinese female donor
Wang S et al. Establishment of an induced pluripotent stem cell line (SDCHi011-A) from a healthy Chinese female donor. . 2024-12-00. Pubmed ID: 39461115; DOI: 10.1016/j.scr.2024.103588 SDCHi001-ASDCHi011-A 2024-12-00 2024-12-00 PubMed: 39461115 DOI: 10.1016/j.scr.2024.103588Associated cell lines:
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Shao J, Shao C, Yang G, Jin Y
Establishing an induced pluripotent stem cell line (SDPHi006-A) from a healthy Chinese female donor represents an accomplishment
Shao J et al. Establishing an induced pluripotent stem cell line (SDPHi006-A) from a healthy Chinese female donor represents an accomplishment. . 2024-12-00. Pubmed ID: 39454534; DOI: 10.1016/j.scr.2024.103590 SDQLCHi025-ASDPHi005-ASDPHi006-A 2024-12-00 2024-12-00 PubMed: 39454534 DOI: 10.1016/j.scr.2024.103590Associated cell lines:
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Fekadu-Siebald Julia, Fuchs Nina V, Zahn Stella, Rommel Marcel G E, Schenk Franziska, Huenecke Sabine, Bremm Melanie, Kreyenberg Hermann, Kuci Zyrafete, Jacobsen Eva-Maria, Hoenig Manfred, Schwarz Klaus, Bader Peter, Modlich Ute, König Renate, Bakhtiar Shahrzad
Eight induced pluripotent stem cell lines (iPSCs) derived from two patients with Leukocyte adhesion deficiency Type I (LAD I) with mutations in the ITGB2 gene
Fekadu-Siebald Julia et al. Eight induced pluripotent stem cell lines (iPSCs) derived from two patients with Leukocyte adhesion deficiency Type I (LAD I) with mutations in the ITGB2 gene. . 2024-12-00. DOI: 10.1016/j.scr.2024.103598 PEIi003-A 2024-12-00 2024-12-00 DOI: 10.1016/j.scr.2024.103598Associated cell lines:
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Liang Yuqin, Sun Xihao, Chen Hang, Cui Zekai, Gu Jianing, Duan Chunwen, Mao Shengru, Chen Yuexi, Li Xiaoxue, Xiong Siqi, Chen Jiansu
CRISPR/Cas9-mediated generation of a human induced pluripotent stem cell line with PRPF6 c.2699 G > A mutation to model retinitis pigmentosa
Liang Yuqin et al. CRISPR/Cas9-mediated generation of a human induced pluripotent stem cell line with PRPF6 c.2699 G > A mutation to model retinitis pigmentosa. . 2024-12-00. DOI: 10.1016/j.scr.2024.103581 CSUASOi004-ACSUASOi004-A-1CSUASOi012-A 2024-12-00 2024-12-00 DOI: 10.1016/j.scr.2024.103581Associated cell lines:
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Guo X, Zhang M, Xu Z, Yu Y, Shen Z
CRISPR/Cas9-mediated generation of AP-1 activity reporter cell line in human embryonic stem cell (WAe007-A-5)
Guo X et al. CRISPR/Cas9-mediated generation of AP-1 activity reporter cell line in human embryonic stem cell (WAe007-A-5). . 2024-12-00. Pubmed ID: 39276528; DOI: 10.1016/j.scr.2024.103557 WAe007-AWAe007-A-5 2024-12-00 2024-12-00 PubMed: 39276528 DOI: 10.1016/j.scr.2024.103557Associated cell lines:
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Kim AH, Lee HM, Kim HS, Jeong SW, Jun JK, Jang J
CRISPR/Cas9-mediated knock-in of a fluorescent reporter into the target locus of interest in human pluripotent stem cells
Kim AH et al. CRISPR/Cas9-mediated knock-in of a fluorescent reporter into the target locus of interest in human pluripotent stem cells. . 2024-12-00. Pubmed ID: 39036607; DOI: 10.1016/j.mex.2024.102807; PMC: PMC11259911 SNUe003-ASNUe003-A-3 2024-12-00 2024-12-00 PubMed: 39036607 DOI: 10.1016/j.mex.2024.102807Associated cell lines:
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Treschow AF, Vinggaard AM, Valente MJ
Standardization and optimization of the hiPSC-based PluriLum assay for detection of embryonic and developmental toxicants
Treschow AF et al. Standardization and optimization of the hiPSC-based PluriLum assay for detection of embryonic and developmental toxicants. . 2024-12-00. Pubmed ID: 39365317; DOI: 10.1007/s00204-024-03870-8; PMC: PMC11496362 BIONi010-C 2024-12-00 2024-12-00 PubMed: 39365317 DOI: 10.1007/s00204-024-03870-8Associated cell lines:
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Hu B, Wang Z, Ma T, Fan P, Li L
Research progress on the pathogenesis of multiple symmetrical lipomatosis
Hu B et al. Research progress on the pathogenesis of multiple symmetrical lipomatosis. . 2024-12-00. Pubmed ID: 39648639; DOI: 10.1080/21623945.2024.2416681; PMC: PMC11487982 JUCTCi012-A 2024-12-00 2024-12-00 PubMed: 39648639 DOI: 10.1080/21623945.2024.2416681Associated cell lines:
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Dwojak E, O'Mard D, Zou J, Wassif CA, Burkett S, Eckhaus M, Rueda Faucz F, Padilla C, Villasmil R, Zheng W, Dang Do AN
Six induced pluripotent stem cell lines from fibroblasts of individuals with CLN3-related conditions
Dwojak E et al. Six induced pluripotent stem cell lines from fibroblasts of individuals with CLN3-related conditions. . 2024-12-00. Pubmed ID: 39317061; DOI: 10.1016/j.scr.2024.103563; PMC: PMC11645225 TRNDi010-CCHDTRi001-BCHDTRi002-BCHDTRi003-ACHDTRi004-BCHDTRi005-ACHDTRi006-E 2024-12-00 2024-12-00 PubMed: 39317061 DOI: 10.1016/j.scr.2024.103563Associated cell lines:
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Hou X, Wang Z, Guo R, Zhou Z, Zhang J, Li Y, Yao Akogo H, Ma J, Chen W, Sun D, Ma J, Guo Q, Cui H
Derivation of induced pluripotent stem cell from a Baraitser-Winter Cerebrofrontofacial syndrome with ACTB mutation
Hou X et al. Derivation of induced pluripotent stem cell from a Baraitser-Winter Cerebrofrontofacial syndrome with ACTB mutation. . 2024-12-00. Pubmed ID: 39437565; DOI: 10.1016/j.scr.2024.103577 DHMCi005-AHEBHMUi001-AHEBHMUi018-A 2024-12-00 2024-12-00 PubMed: 39437565 DOI: 10.1016/j.scr.2024.103577Associated cell lines:
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Wu Y, Meng XY, Sun HF, Zhang YJ, Liu XH, Wang DD, Liu DH, Li SM, Li JK, Li WX, Li SA, Liu PP, Kang JS
Construction of induced pluripotent stem cell line (CSBZZUi002-A) from the fibroblast cells of a healthy female
Wu Y et al. Construction of induced pluripotent stem cell line (CSBZZUi002-A) from the fibroblast cells of a healthy female. . 2024-12-00. Pubmed ID: 39442281; DOI: 10.1016/j.scr.2024.103593 ZZUi019-AZZUi031-ACSBZZUi002-A 2024-12-00 2024-12-00 PubMed: 39442281 DOI: 10.1016/j.scr.2024.103593Associated cell lines:
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Zhang C, Li J, Sai Y, Su H, Jiang Y, Zhang L, Jian L, Zhang H, Guo G, Li E, Li X, Sun L
Establishment of heterozygous LMOD2 knockout human embryonic stem cell line (ZZUNEUi022-A-1) using CRISPR/Cas9 system
Zhang C et al. Establishment of heterozygous LMOD2 knockout human embryonic stem cell line (ZZUNEUi022-A-1) using CRISPR/Cas9 system. . 2024-12-00. Pubmed ID: 39437564; DOI: 10.1016/j.scr.2024.103586 ZZUNEUi022-AZZUNEUi022-A-1 2024-12-00 2024-12-00 PubMed: 39437564 DOI: 10.1016/j.scr.2024.103586Associated cell lines:
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Ruan J, Wu M, Xiang J, Hui X, Yang L, Lin R, Xu W, Shu Q
Generation of a human induced pluripotent stem cell line from a female patient carrying LZTR1 gene mutation
Ruan J et al. Generation of a human induced pluripotent stem cell line from a female patient carrying LZTR1 gene mutation. . 2024-12-00. Pubmed ID: 39577308; DOI: 10.1016/j.scr.2024.103616 CHZJUi001-A 2024-12-00 2024-12-00 PubMed: 39577308 DOI: 10.1016/j.scr.2024.103616Associated cell lines:
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Leavens Karla F., Osorio-Quintero Catherine, Yeuteuh Elisabeth Ashlyne, Perez-Profeta Francesca T., Dattoli Anna Ada, Cardenas-Diaz Fabian L., French Deborah L., Gadue Paul
Generation of a fluorescent mNeonGreen insulin reporter line in the H1 (WA01) hESC background
Leavens Karla F. et al. Generation of a fluorescent mNeonGreen insulin reporter line in the H1 (WA01) hESC background. . 2024-12-00. DOI: 10.1016/j.scr.2024.103559 CHOPi002-ACHOPi003-A 2024-12-00 2024-12-00 DOI: 10.1016/j.scr.2024.103559Associated cell lines:
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Xi S, Xue B, Wang Y, Shan Z, Song T, Sun J, Qin S
Generation of patient-derived induced pluripotent stem cell line UJSi004-A from ultra-treatment-resistant schizophrenia
Xi S et al. Generation of patient-derived induced pluripotent stem cell line UJSi004-A from ultra-treatment-resistant schizophrenia. . 2024-12-00. Pubmed ID: 39423675; DOI: 10.1016/j.scr.2024.103575 UJSi001-AUJSi002-AUJSi004-A 2024-12-00 2024-12-00 PubMed: 39423675 DOI: 10.1016/j.scr.2024.103575 -
Lee Y, Park HJ, Kim YO, Kim BY
Generation of a human induced pluripotent stem cell line (KSCBi016-A) from a CPVT patient with an RYR2 mutation
Lee Y et al. Generation of a human induced pluripotent stem cell line (KSCBi016-A) from a CPVT patient with an RYR2 mutation. . 2024-12-00. Pubmed ID: 39321749; DOI: 10.1016/j.scr.2024.103560 KSCBi016-A 2024-12-00 2024-12-00 PubMed: 39321749 DOI: 10.1016/j.scr.2024.103560Associated cell lines:
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Mengnan W, Yan C, Qiong X, Man X
Generation of a human induced pluripotent stem cell line (FDIBSi001-A) from a patient with ADNP syndrome carrying ADNP mutation (c. 2059 T>C)
Mengnan W et al. Generation of a human induced pluripotent stem cell line (FDIBSi001-A) from a patient with ADNP syndrome carrying ADNP mutation (c. 2059 T>C). . 2024-12-00. Pubmed ID: 39307104; DOI: 10.1016/j.scr.2024.103550 FDIBSi001-A 2024-12-00 2024-12-00 PubMed: 39307104 DOI: 10.1016/j.scr.2024.103550Associated cell lines:
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Weng Shiwen, Liu Xiang, Wang Dayan, Wang Jiaxuan, Ren Qian, Wang Qun, Shan Wei
Generation of a human induced pluripotent stem cell (iPSC) line from a patient with a CDKL5 gene mutation
Weng Shiwen et al. Generation of a human induced pluripotent stem cell (iPSC) line from a patient with a CDKL5 gene mutation. . 2024-12-00. DOI: 10.1016/j.scr.2024.103607 HMSCATi006-A 2024-12-00 2024-12-00 DOI: 10.1016/j.scr.2024.103607Associated cell lines:
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Srisantitham J, Suwanpitak S, Thongsin N, Wattanapanitch M
Generation of a homozygous TIGIT gene knockout (TIGIT(-/-)) human iPSC line (MUSIi001-A-3) using CRISPR/Cas9 system
Srisantitham J et al. Generation of a homozygous TIGIT gene knockout (TIGIT(-/-)) human iPSC line (MUSIi001-A-3) using CRISPR/Cas9 system. . 2024-12-00. Pubmed ID: 39476616; DOI: 10.1016/j.scr.2024.103601 MUSIi001-AMUSIi001-A-3 2024-12-00 2024-12-00 PubMed: 39476616 DOI: 10.1016/j.scr.2024.103601Associated cell lines:
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Kang Y, Liang S, Gao S, Chen J
Generation of a hiPSC line (TONGJIi001-A) from a 46,XX,ins(1;15)(p13.3; q22.31q26.1),inv(2)(p22.1p16.3),t(2;14)(q34;q12) infertility patient
Kang Y et al. Generation of a hiPSC line (TONGJIi001-A) from a 46,XX,ins(1;15)(p13.3; q22.31q26.1),inv(2)(p22.1p16.3),t(2;14)(q34;q12) infertility patient. . 2024-12-00. Pubmed ID: 39299133; DOI: 10.1016/j.scr.2024.103561 TONGJIi001-A 2024-12-00 2024-12-00 PubMed: 39299133 DOI: 10.1016/j.scr.2024.103561Associated cell lines:
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Syed Ali G, Rebs S, Eberl H, Zinke C, Hübscher D, Maurer W, Busley A, Cyganek L, Streckfuss-Bömeke K
Generation of a heterozygous Calsequestrin 2 F189L iPSC line (UMGi158-B) by CRISPR/Cas9 genome editing to investigate the cardiac pathophysiology of Takotsubo Syndrome and Catecholaminergic Polymorphic Ventricular Tachycardia
Syed Ali G et al. Generation of a heterozygous Calsequestrin 2 F189L iPSC line (UMGi158-B) by CRISPR/Cas9 genome editing to investigate the cardiac pathophysiology of Takotsubo Syndrome and Catecholaminergic Polymorphic Ventricular Tachycardia. . 2024-12-00. Pubmed ID: 39378715; DOI: 10.1016/j.scr.2024.103538 UMGi158-B 2024-12-00 2024-12-00 PubMed: 39378715 DOI: 10.1016/j.scr.2024.103538Associated cell lines:
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Sun X, Liang Y, Duan C, Liu X, Zhou Y, Mao S, Cui Z, Gu J, Ding C, Chen J, Tang S
Generation of a gene-corrected isogenic human iPSC line (CSUASOi006-A-1) from a retinitis pigmentosa patient with heterozygous c.5792C > T mutation in the PRPF8 gene
Sun X et al. Generation of a gene-corrected isogenic human iPSC line (CSUASOi006-A-1) from a retinitis pigmentosa patient with heterozygous c.5792C > T mutation in the PRPF8 gene. . 2024-12-00. Pubmed ID: 39388803; DOI: 10.1016/j.scr.2024.103572 CSUASOi006-ACSUASOi006-A-1 2024-12-00 2024-12-00 PubMed: 39388803 DOI: 10.1016/j.scr.2024.103572Associated cell lines:
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De Serres-Bérard T, Pouliot V, Puymirat J, Chahine M
Generation of a control induced pluripotent stem cell line (CBRCULi014-A) derived from the lymphoblastoid cells of a pediatric individual
De Serres-Bérard T et al. Generation of a control induced pluripotent stem cell line (CBRCULi014-A) derived from the lymphoblastoid cells of a pediatric individual. . 2024-12-00. Pubmed ID: 39471665; DOI: 10.1016/j.scr.2024.103587 CBRCULi001-ACBRCULi002-ACBRCULi003-ACBRCULi004-ACBRCULi005-ACBRCULi014-ACBRCULi015-A 2024-12-00 2024-12-00 PubMed: 39471665 DOI: 10.1016/j.scr.2024.103587Associated cell lines:
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Jager Joanna, Ribeiro Marta, Furtado Marta, Carvalho Teresa, Syrris Petros, Lopes Luis R., Elliott Perry M., Cabral Joaquim M.S., Carmo-Fonseca Maria, da Rocha Simão Teixeira, Martins Sandra
Patient-derived induced pluripotent stem cells to study non-canonical splicing variants associated with Hypertrophic Cardiomyopathy
Jager Joanna et al. Patient-derived induced pluripotent stem cells to study non-canonical splicing variants associated with Hypertrophic Cardiomyopathy. . 2024-12-00. DOI: 10.1016/j.scr.2024.103582 SCVIi001-ASCVIi002-A 2024-12-00 2024-12-00 DOI: 10.1016/j.scr.2024.103582Associated cell lines:
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Pachis ST, Ramovs V, Freund C, Has C, Raymond K
Generation and genetic repair of two human induced pluripotent stem cell lines from patients with Epidermolysis Bullosa simplex associated with a heterozygous mutation in the translation initiation codon of KLHL24
Pachis ST et al. Generation and genetic repair of two human induced pluripotent stem cell lines from patients with Epidermolysis Bullosa simplex associated with a heterozygous mutation in the translation initiation codon of KLHL24. . 2024-12-00. Pubmed ID: 39317060; DOI: 10.1016/j.scr.2024.103551 LUMCi058-ALUMCi059-ALUMCi058-A-1LUMCi059-A-1 2024-12-00 2024-12-00 PubMed: 39317060 DOI: 10.1016/j.scr.2024.103551Associated cell lines:
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Ferreira A, Calado SM, Jorge X, de Lange J, Carvalhal S
Generation and characterization of two isogenic induced pluripotent stem cell lines from a young female with microcephaly carrying a compound heterozygous mutation in BUB1 gene
Ferreira A et al. Generation and characterization of two isogenic induced pluripotent stem cell lines from a young female with microcephaly carrying a compound heterozygous mutation in BUB1 gene. . 2024-12-00. Pubmed ID: 39490209; DOI: 10.1016/j.scr.2024.103594 UALGi003-AUALGi003-B 2024-12-00 2024-12-00 PubMed: 39490209 DOI: 10.1016/j.scr.2024.103594Associated cell lines:
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Naidoo J, Hurrell T, Scholefield J
The generation of human induced pluripotent stem cell lines from individuals of Black African ancestry in South Africa
Naidoo J et al. The generation of human induced pluripotent stem cell lines from individuals of Black African ancestry in South Africa. . 2024-12-00. Pubmed ID: 39146664; DOI: 10.1016/j.scr.2024.103534 CSIRi001-ACSIRi001-BCSIRi002-ACSIRi002-B 2024-12-00 2024-12-00 PubMed: 39146664 DOI: 10.1016/j.scr.2024.103534Associated cell lines:
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Davidenko Alina, Bogomazova Alexandra, Illarioshkin Sergey, Lagarkova Maria
Molecular Mechanisms of Spinocerebellar Ataxia Type 17
Davidenko Alina et al. Molecular Mechanisms of Spinocerebellar Ataxia Type 17. . 2024-11-30. DOI: 10.1007/s12035-024-04645-z RCPCMi008-A 2024-11-30 2024-11-30 DOI: 10.1007/s12035-024-04645-zAssociated cell lines:
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Zhang Hao, Thai Phung N., Shivnaraine Rabindra V., Ren Lu, Wu Xuekun, Siepe Dirk H., Liu Yu, Tu Chengyi, Shin Hye Sook, Caudal Arianne, Mukherjee Souhrid, Leitz Jeremy, Wen Wilson Tan Lek, Liu Wenqiang, Zhu Wenjuan, Chiamvimonvat Nipavan, Wu Joseph C.
Multiscale drug screening for cardiac fibrosis identifies MD2 as a therapeutic target
Zhang Hao et al. Multiscale drug screening for cardiac fibrosis identifies MD2 as a therapeutic target. . 2024-12-00. DOI: 10.1016/j.cell.2024.09.034 SCVIi014-ASCVIi015-ASCVIi016-A 2024-12-00 2024-12-00 DOI: 10.1016/j.cell.2024.09.034Associated cell lines:
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Song Xiao-Yan, Fan Cun-xiu, Atta-ur-Rahman, Choudhary Muhammad Iqbal, Wang Xiao-Ping
Neuro-regeneration or Repair: Cell Therapy of Neurological Disorders as A Way Forward
Song Xiao-Yan et al. Neuro-regeneration or Repair: Cell Therapy of Neurological Disorders as A Way Forward. . 2024-12-00. DOI: 10.2174/1570159x22666240509092903 THSJTUi001-A 2024-12-00 2024-12-00 DOI: 10.2174/1570159x22666240509092903Associated cell lines:
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Mun D, Yoo G, Park M, Kang JY, Yun N, Joung B
Establishment of two human induced pluripotent stem cell lines from familial long QT syndrome type 1 patients carrying KCNQ1 mutation
Mun D et al. Establishment of two human induced pluripotent stem cell lines from familial long QT syndrome type 1 patients carrying KCNQ1 mutation. . 2024-12-00. Pubmed ID: 39388802; DOI: 10.1016/j.scr.2024.103571 YUCMi024-AYUCMi025-A 2024-12-00 2024-12-00 PubMed: 39388802 DOI: 10.1016/j.scr.2024.103571Associated cell lines:
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Fetisoa Monia Ravelonandrasana, Acheampong Adolf, Bondzie-Quaye Precious, Bashir Mona Alrasheed, Huang Qing
Synergistic strategies for optimizing microalgae-based wastewater treatment: a comprehensive review
Fetisoa Monia Ravelonandrasana et al. Synergistic strategies for optimizing microalgae-based wastewater treatment: a comprehensive review. . 2024-12-00. DOI: 10.1016/j.jwpe.2024.106409 ZZUNEUi026-A 2024-12-00 2024-12-00 DOI: 10.1016/j.jwpe.2024.106409Associated cell lines:
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Guan J, Duan C, Lv Y, Zhang H, Liu G, Liu Y
Establishment of iPS cell line (SDQLCHi080-A) from a patient with GM1 gangliosidosis due to GLB1 mutation
Guan J et al. Establishment of iPS cell line (SDQLCHi080-A) from a patient with GM1 gangliosidosis due to GLB1 mutation. . 2024-12-00. Pubmed ID: 39213692; DOI: 10.1016/j.scr.2024.103545 SDQLCHi080-A 2024-12-00 2024-12-00 PubMed: 39213692 DOI: 10.1016/j.scr.2024.103545Associated cell lines:
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Pavlova S, Shulgina A, Minina J, Zakian S, Dementyeva E.
Generation of Isogenic iPSC Lines for Studying the Effect of the p.N515del (c.1543_1545delAAC) Variant on MYBPC3 Function and Hypertrophic Cardiomyopathy Pathogenesis
Pavlova S et al. Generation of Isogenic iPSC Lines for Studying the Effect of the p.N515del (c.1543_1545delAAC) Variant on MYBPC3 Function and Hypertrophic Cardiomyopathy Pathogenesis. . 2024-11-30. Pubmed ID: 39684611; DOI: 10.3390/ijms252312900; PMC: PMC11641397 ICGi022-AICGi029-AICGi022-A-3ICGi022-A-4ICGi022-A-5ICGi029-A-1ICGi029-A-2ICGi029-A-3 2024-11-30 2024-11-30 PubMed: 39684611 DOI: 10.3390/ijms252312900Associated cell lines:
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Sharaf A, Frimat JP, Accardo A
Mechanical confinement matters: Unveiling the effect of two-photon polymerized 2.5D and 3D microarchitectures on neuronal YAP expression and neurite outgrowth
Sharaf A et al. Mechanical confinement matters: Unveiling the effect of two-photon polymerized 2.5D and 3D microarchitectures on neuronal YAP expression and neurite outgrowth. . 2024-12-00. Pubmed ID: 39569166; DOI: 10.1016/j.mtbio.2024.101325; PMC: PMC11576396 LUMCi003-A 2024-12-00 2024-12-00 PubMed: 39569166 DOI: 10.1016/j.mtbio.2024.101325Associated cell lines:
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Sun H, Li Q, Xu T, Zhang W, Sun J, Liu H
Generation of SFTPC-mCherry knock-in reporter human embryonic stem cell line, WAe001-A-2H, using CRISPR/Cas9-based gene targeting
Sun H et al. Generation of SFTPC-mCherry knock-in reporter human embryonic stem cell line, WAe001-A-2H, using CRISPR/Cas9-based gene targeting. . 2024-12-00. Pubmed ID: 39476617; DOI: 10.1016/j.scr.2024.103597 WAe001-AWAe001-A-2H 2024-12-00 2024-12-00 PubMed: 39476617 DOI: 10.1016/j.scr.2024.103597Associated cell lines:
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Haferkamp U, Telugu N, Krieg K, Schaefer W, Lam D, Binkle-Ladisch L, Friese MA, Diecke S, Pless O
Generation of two isogenic human iPSC lines (ZIPi013-B-1, ZIPi013-B-2) carrying a CRISPR/Cas9-mediated deletion of TRPM4
Haferkamp U et al. Generation of two isogenic human iPSC lines (ZIPi013-B-1, ZIPi013-B-2) carrying a CRISPR/Cas9-mediated deletion of TRPM4. . 2024-12-00. Pubmed ID: 39546944; DOI: 10.1016/j.scr.2024.103609 UKBi011-AZIPi013-BZIPi013-B-1ZIPi013-B-2 2024-12-00 2024-12-00 PubMed: 39546944 DOI: 10.1016/j.scr.2024.103609Associated cell lines:
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Devito LG, Lim ES, O'Toole SM, Shepherd STC, Deng D, Feng H, Barber T, Drake WM, Turajlic S, Healy L
Generation of TWO iPSC lines (CRICKi009-A; CRICKi010-A) from patients with type 1 von Hippel-Lindau (VHL) and histopathologically confirmed renal cell carcinoma (RCC)
Devito LG et al. Generation of TWO iPSC lines (CRICKi009-A; CRICKi010-A) from patients with type 1 von Hippel-Lindau (VHL) and histopathologically confirmed renal cell carcinoma (RCC). . 2024-12-00. Pubmed ID: 39549334; DOI: 10.1016/j.scr.2024.103611 CRICKi001-ACRICKi009-ACRICKi010-A 2024-12-00 2024-12-00 PubMed: 39549334 DOI: 10.1016/j.scr.2024.103611Associated cell lines:
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Sun J, Ren L, Canel Rivero G, Xu L, Ladabaum U, C Wu J
Generation of two induced pluripotent stem cell lines from patients with Li-Fraumeni Syndrome carrying TP53 mutation
Sun J et al. Generation of two induced pluripotent stem cell lines from patients with Li-Fraumeni Syndrome carrying TP53 mutation. . 2024-12-00. Pubmed ID: 39133963; DOI: 10.1016/j.scr.2024.103527 SCVIi104-ASCVIi105-A 2024-12-00 2024-12-00 PubMed: 39133963 DOI: 10.1016/j.scr.2024.103527Associated cell lines:
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Naigles Beverly, Soroczynski Jan, Hao Nan
Genetic Knock-Ins of Endogenous Fluorescent Tags in RAW 264.7 Murine Macrophages Using CRISPR/Cas9 Genome Editing
Naigles Beverly et al. Genetic Knock-Ins of Endogenous Fluorescent Tags in RAW 264.7 Murine Macrophages Using CRISPR/Cas9 Genome Editing. . 2025-00-00. DOI: 10.21769/bioprotoc.4960 KITi001-AKITi001-A-1 2025-00-00 2025-00-00 DOI: 10.21769/bioprotoc.4960Associated cell lines:
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Giovenale AMG, Turco EM, Mazzoni M, Ferrone I, Torres B, Bernardini L, Vulcano E, Ferrari D, Onesimo R, D'Arrigo S, Zampino G, Pennuto M, De Luca A, Vescovi AL, Rosati J
Generation of the CSSi020-A (14437) iPSC line from a patient carrying a copy number variation (CNV) in the 17p11.2 chromosome region
Giovenale AMG et al. Generation of the CSSi020-A (14437) iPSC line from a patient carrying a copy number variation (CNV) in the 17p11.2 chromosome region. . 2024-12-00. Pubmed ID: 39260069; DOI: 10.1016/j.scr.2024.103544 CSSi013-ACSSi020-A 2024-12-00 2024-12-00 PubMed: 39260069 DOI: 10.1016/j.scr.2024.103544 -
Widyastuti HP, van der Vaart B, Pachis ST, Freund C, Gidrol X, Raymond K
Generation of XPA p.Arg228T mutant LUMCi004-A cell line for modeling Xeroderma pigmentosum group A
Widyastuti HP et al. Generation of XPA p.Arg228T mutant LUMCi004-A cell line for modeling Xeroderma pigmentosum group A. . 2024-12-00. Pubmed ID: 39321748; DOI: 10.1016/j.scr.2024.103564 LUMCi004-ALUMCi004-A-3 2024-12-00 2024-12-00 PubMed: 39321748 DOI: 10.1016/j.scr.2024.103564Associated cell lines:
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Chen W, Wang H, Zhu K, Wang T, Yu W, Wu Q
Generation of the TSHSUi002-A induced pluripotent stem cell line from a patient with Peutz-Jeghers syndrome carring STK11 gene mutation
Chen W et al. Generation of the TSHSUi002-A induced pluripotent stem cell line from a patient with Peutz-Jeghers syndrome carring STK11 gene mutation. . 2024-12-00. Pubmed ID: 39603093; DOI: 10.1016/j.scr.2024.103618 TSHSUi002-A 2024-12-00 2024-12-00 PubMed: 39603093 DOI: 10.1016/j.scr.2024.103618Associated cell lines:
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Guo Fuying, Xu Ping, Zheng Dandan, Zhong Xiufeng
Generation of two hiPSC lines carrying compound heterozygous RDH12 mutations in a LCA patient
Guo Fuying et al. Generation of two hiPSC lines carrying compound heterozygous RDH12 mutations in a LCA patient. . 2024-12-00. DOI: 10.1016/j.scr.2024.103525 UCLi014-AUCLi015-A 2024-12-00 2024-12-00 DOI: 10.1016/j.scr.2024.103525 -
Lee SE, Park S, Kang R, Lee T, Yu WJ, Chang S, Park JC
Hippocampal tau-induced GRIN3A deficiency in Alzheimer's disease
Lee SE et al. Hippocampal tau-induced GRIN3A deficiency in Alzheimer's disease. . 2024-12-00. Pubmed ID: 39396906; DOI: 10.1002/2211-5463.13904; PMC: PMC11609574 BIONi010-C 2024-12-00 2024-12-00 PubMed: 39396906 DOI: 10.1002/2211-5463.13904Associated cell lines:
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Vincent Ambily, Krishnakumar Subramanian, Parameswaran Sowmya
Heterozygous RB1 mutation enhanced ATP production in human iPSC-derived retinal organoids
Vincent Ambily et al. Heterozygous RB1 mutation enhanced ATP production in human iPSC-derived retinal organoids. . 2024-12-00. DOI: 10.1007/s11033-024-09564-9 VRFi001-A 2024-12-00 2024-12-00 DOI: 10.1007/s11033-024-09564-9Associated cell lines:
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Sundstrom J, Vanderleeden E, Barton N, Redick S, Dawes P, Murray L, Olson M, Tran K, Chigas S, Orszulak A, Church G, Readhead B, Oh H, Harlan D, Knipe D, Wang J, Chan Y, Lim E.
Herpes Simplex Virus 1 Infection of Human Brain Organoids and Pancreatic Stem Cell-Islets Drives Organoid-Specific Transcripts Associated with Alzheimer’s Disease and Autoimmune Diseases
Sundstrom J et al. Herpes Simplex Virus 1 Infection of Human Brain Organoids and Pancreatic Stem Cell-Islets Drives Organoid-Specific Transcripts Associated with Alzheimer’s Disease and Autoimmune Diseases. . 2024-11-29. HVRDe008-AHVRDe008-A-1 2024-11-29 2024-11-29Associated cell lines:
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Sundstrom J, Vanderleeden E, Barton NJ, Redick SD, Dawes P, Murray LF, Olson MN, Tran K, Chigas SM, Orszulak AR, Church GM, Readhead B, Oh HS, Harlan DM, Knipe DM, Wang JP, Chan Y, Lim ET
Herpes Simplex Virus 1 Infection of Human Brain Organoids and Pancreatic Stem Cell-Islets Drives Organoid-Specific Transcripts Associated with Alzheimer's Disease and Autoimmune Diseases
Sundstrom J et al. Herpes Simplex Virus 1 Infection of Human Brain Organoids and Pancreatic Stem Cell-Islets Drives Organoid-Specific Transcripts Associated with Alzheimer's Disease and Autoimmune Diseases. . 2024-11-29. Pubmed ID: 39682726; DOI: 10.3390/cells13231978; PMC: PMC11640215 HVRDe008-AHVRDe008-A-1 2024-11-29 2024-11-29 PubMed: 39682726 DOI: 10.3390/cells13231978Associated cell lines:
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Maione Angela Serena, Iengo Lara, Sala Luca, Massaiu Ilaria, Chiesa Mattia, Lippi Melania, Ghilardi Stefania, Florindi Chiara, Lodola Francesco, Zaza Antonio, Tondo Claudio, Schiavone Marco, Banfi Cristina, Pompilio Giulio, Poggio Paolo, Sommariva Elena
Cardiomyocyte and stromal cell cross-talk influences the pathogenesis of arrhythmogenic cardiomyopathy: a multi-level analysis uncovers DLK1-NOTCH pathway role in fibro-adipose remodelling
Maione Angela Serena et al. Cardiomyocyte and stromal cell cross-talk influences the pathogenesis of arrhythmogenic cardiomyopathy: a multi-level analysis uncovers DLK1-NOTCH pathway role in fibro-adipose remodelling. . 2024-11-28. DOI: 10.1038/s41420-024-02232-8 LUMCi027-A 2024-11-28 2024-11-28 DOI: 10.1038/s41420-024-02232-8Associated cell lines:
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Chao Clifford, Martinez Isabella G., Wagenblast Elvin
Models to study myelodysplastic syndrome and acute myeloid leukaemia
Chao Clifford et al. Models to study myelodysplastic syndrome and acute myeloid leukaemia. . 2024-11-28. DOI: 10.1097/moh.0000000000000856 ESi086-AESi086-A-3 2024-11-28 2024-11-28 DOI: 10.1097/moh.0000000000000856Associated cell lines:
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Akerman Emily, Capel Rebecca A, Read Matthew, Song Qianqian, Bose Samuel J, Calamaio Serena, Aston Daniel, Koschinski Andreas, Lloyd Scott, Bell Laura, Rashbrook Victoria S, Keller Marco, Bracher Franz, Potter Barry VL, Rivolta Ilaria, Galione Antony, Sparrow Duncan B, Conti Alana, Terrar Derek A, Zaccolo Manuela, Burton Rebecca AB
Lysosomal calcium signalling contributes to the acute α-adrenergic response via calcium-stimulated adenylyl cyclase 1 and 8
Akerman Emily et al. Lysosomal calcium signalling contributes to the acute α-adrenergic response via calcium-stimulated adenylyl cyclase 1 and 8. . 2024-11-26. DOI: 10.1101/2024.11.25.625232 TMOi001-A 2024-11-26 2024-11-26 DOI: 10.1101/2024.11.25.625232Associated cell lines:
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Matsuyama Makoto, Iwamiya Takahiro
Novel and effective plasmid transfection protocols for functional analysis of genetic elements in human cardiac fibroblasts
Matsuyama Makoto et al. Novel and effective plasmid transfection protocols for functional analysis of genetic elements in human cardiac fibroblasts. . 2024-11-26. DOI: 10.1371/journal.pone.0309566 CBTCi001-A 2024-11-26 2024-11-26 DOI: 10.1371/journal.pone.0309566Associated cell lines:
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Costa A, Hunkler HJ, Chatterjee S, Cushman S, Hilbold E, Xiao K, Lu D, Leonardy J, Juchem M, Sansonetti M, Hoepfner J, Thum T, Bär C
A reporter system for live cell tracking of human cardiomyocyte proliferation
Costa A et al. A reporter system for live cell tracking of human cardiomyocyte proliferation. . 2024-11-25. Pubmed ID: 39177246; DOI: 10.1093/cvr/cvae175; PMC: PMC11587551 MHHi001-AMHHi001-A-3 2024-11-25 2024-11-25 PubMed: 39177246 DOI: 10.1093/cvr/cvae175Associated cell lines:
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Siehler Johanna, Bilekova Sara, Chapouton Prisca, Dema Alessandro, Albanese Pascal, Tamara Sem, Jain Chirag, Sterr Michael, Enos Stephen J., Chen Chunguang, Malhotra Chetna, Villalba Adrian, Schomann Leopold, Bhattacharya Sreya, Feng Jin, Akgün Canan Melis, Ribaudo Federico, Ansarullah, Burtscher Ingo, Ahlbrecht Christin, Plettenburg Oliver, Kurth Thomas, Scharfmann Raphael, Speier Stephan, Scheltema Richard A., Lickert Heiko
Inceptor binds to and directs insulin towards lysosomal degradation in β cells
Siehler Johanna et al. Inceptor binds to and directs insulin towards lysosomal degradation in β cells. . 2024-11-25. DOI: 10.1038/s42255-024-01164-y HMGUi001-AHMGUi001-A-8 2024-11-25 2024-11-25 DOI: 10.1038/s42255-024-01164-yAssociated cell lines:
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Marcella BM, Hockey BL, Braun JL, Whitley KC, Geromella MS, Baranowski RW, Watson CJF, Silvera S, Hamstra SI, Wasilewicz LJ, Crozier RWE, Marais AAT, Kim KH, Lee G, Vandenboom R, Roy BD, MacNeil AJ, MacPherson REK, Fajardo VA
GSK3 inhibition improves skeletal muscle function and whole-body metabolism in male mouse models of Duchenne muscular dystrophy
Marcella BM et al. GSK3 inhibition improves skeletal muscle function and whole-body metabolism in male mouse models of Duchenne muscular dystrophy. . 2024-11-25. Pubmed ID: 39587049; DOI: 10.1038/s41467-024-53886-y; PMC: PMC11589163 WAe009-A 2024-11-25 2024-11-25 PubMed: 39587049 DOI: 10.1038/s41467-024-53886-yAssociated cell lines:
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Dionne Olivier, Sabatié Salomé, Fortin Fléchère, Corbin François, Laurent Benoit
Efficient generation of human induced pluripotent stem cells from urine samples of patients with Fragile X syndrome
Dionne Olivier et al. Efficient generation of human induced pluripotent stem cells from urine samples of patients with Fragile X syndrome. . 2024-11-22. DOI: 10.3389/fcell.2024.1489190 KEIOi005-A 2024-11-22 2024-11-22 DOI: 10.3389/fcell.2024.1489190Associated cell lines:
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Sheveleva O, Protasova E, Grigor'eva E, Butorina N, Kuziaeva V, Antonov D, Melnikova V, Medvedev S, Lyadova I
The Generation of Genetically Engineered Human Induced Pluripotent Stem Cells Overexpressing IFN-β for Future Experimental and Clinically Oriented Studies
Sheveleva O et al. The Generation of Genetically Engineered Human Induced Pluripotent Stem Cells Overexpressing IFN-β for Future Experimental and Clinically Oriented Studies. . 2024-11-20. Pubmed ID: 39596521; DOI: 10.3390/ijms252212456; PMC: PMC11595023 ICGi014-AICGi021-AICGi022-AUNIBSi014-ASDQLCHi048-A 2024-11-20 2024-11-20 PubMed: 39596521 DOI: 10.3390/ijms252212456Associated cell lines:
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El-Banna Ahmed H., Abo El-Ela Fatma I., Abdel-Wahab Ahmed, Gamal Amr, Abdel-Razik Abdel-Razik H., El-Banna Hossny A., Elsamannoudy Salma.I., Ibrahim Marwa A., Abdelghany Asmaa K.
Therapeutic efficacy of amygdaline and amygdaline-loaded niosomes in a rat model of Alzheimer’s disease via oxidative stress, brain neurotransmitters, and apoptotic pathway
El-Banna Ahmed H. et al. Therapeutic efficacy of amygdaline and amygdaline-loaded niosomes in a rat model of Alzheimer’s disease via oxidative stress, brain neurotransmitters, and apoptotic pathway. . 2024-11-19. DOI: 10.1186/s43088-024-00573-y IRMBi001-A 2024-11-19 2024-11-19 DOI: 10.1186/s43088-024-00573-yAssociated cell lines:
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Karimpour Sedigheh, De Costa Peter, Nazari Mostafa
Emotions in switching the code: contributions for English language teachers’ identity construction
Karimpour Sedigheh et al. Emotions in switching the code: contributions for English language teachers’ identity construction. . 2024-11-19. DOI: 10.1080/01434632.2024.2429413 ZJSHDPi001-A 2024-11-19 2024-11-19 DOI: 10.1080/01434632.2024.2429413Associated cell lines:
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Tumdam Roshan, Hussein Yara, Garin-Shkolnik Tali, Stern Shani
NMDA Receptors in Neurodevelopmental Disorders: Pathophysiology and Disease Models
Tumdam Roshan et al. NMDA Receptors in Neurodevelopmental Disorders: Pathophysiology and Disease Models. . 2024-11-18. DOI: 10.3390/ijms252212366 BGUi011-ABGUi012-AUNINAi001-AUNINAi002-AUOHi002-AUOHi003-ASDQLCHi051-AGWCMCi006-A 2024-11-18 2024-11-18 DOI: 10.3390/ijms252212366Associated cell lines:
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Peltonen S, Sonninen TM, Niskanen J, Koistinaho J, Ruponen M, Lehtonen Š
Mutated LRRK2 induces a reactive phenotype and alters migration in human iPSC-derived pericyte-like cells
Peltonen S et al. Mutated LRRK2 induces a reactive phenotype and alters migration in human iPSC-derived pericyte-like cells. . 2024-11-18. Pubmed ID: 39551752; DOI: 10.1186/s12987-024-00592-y; PMC: PMC11571670 STBCi004-ASTBCi007-A 2024-11-18 2024-11-18 PubMed: 39551752 DOI: 10.1186/s12987-024-00592-yAssociated cell lines:
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Arber C, Casey JM, Crawford S, Rambarack N, Yaman U, Wiethoff S, Augustin E, Piers TM, Price M, Rostagno A, Ghiso J, Lewis PA, Revesz T, Hardy J, Pocock JM, Houlden H, Schott JM, Salih DA, Lashley T, Wray S
Microglia contribute to the production of the amyloidogenic ABri peptide in familial British dementia
Arber C et al. Microglia contribute to the production of the amyloidogenic ABri peptide in familial British dementia. . 2024-11-15. Pubmed ID: 39546024; DOI: 10.1007/s00401-024-02820-z; PMC: PMC11568029 RBi001-A 2024-11-15 2024-11-15 PubMed: 39546024 DOI: 10.1007/s00401-024-02820-zAssociated cell lines:
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Mothes T, Konstantinidis E, Eltom K, Dakhel A, Rostami J, Erlandsson A
Tau processing and tau-mediated inflammation differ in human APOEε2 and APOEε4 astrocytes
Mothes T et al. Tau processing and tau-mediated inflammation differ in human APOEε2 and APOEε4 astrocytes. . 2024-11-15. Pubmed ID: 39524360; DOI: 10.1016/j.isci.2024.111163; PMC: PMC11549983 BIONi037-ABIONi037-A-2BIONi037-A-4 2024-11-15 2024-11-15 PubMed: 39524360 DOI: 10.1016/j.isci.2024.111163Associated cell lines:
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Iyer DP, Khoei HH, van der Weijden VA, Kagawa H, Pradhan SJ, Novatchkova M, McCarthy A, Rayon T, Simon CS, Dunkel I, Wamaitha SE, Elder K, Snell P, Christie L, Schulz EG, Niakan KK, Rivron N, Bulut-Karslioğlu A
mTOR activity paces human blastocyst stage developmental progression
Iyer DP et al. mTOR activity paces human blastocyst stage developmental progression. . 2024-11-14. Pubmed ID: 39332412; DOI: 10.1016/j.cell.2024.08.048; PMC: PMC7617234 WAe009-A 2024-11-14 2024-11-14 PubMed: 39332412 DOI: 10.1016/j.cell.2024.08.048Associated cell lines:
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Thongsin N, Suwanpitak S, Augsornworawat P, Srisantitham J, Saiprayong K, Jenjaroenpun P, Wattanapanitch M
Phenotypic and transcriptomic profiling of induced pluripotent stem cell (iPSC)-derived NK cells and their cytotoxicity against cancers
Thongsin N et al. Phenotypic and transcriptomic profiling of induced pluripotent stem cell (iPSC)-derived NK cells and their cytotoxicity against cancers. . 2024-11-13. Pubmed ID: 39533434; DOI: 10.1186/s13287-024-04029-z; PMC: PMC11559060 MUSIi001-AMUSIi001-A-1MUSIi001-A-2 2024-11-13 2024-11-13 PubMed: 39533434 DOI: 10.1186/s13287-024-04029-zAssociated cell lines:
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Ge N, Suzuki K, Sato I, Noguchi M, Nakamura Y, Matsuo-Takasaki M, Fujishiro J, Hayashi Y
Generation of human induced pluripotent stem cell lines derived from patients of cystic biliary atresia
Ge N et al. Generation of human induced pluripotent stem cell lines derived from patients of cystic biliary atresia. . 2024-11-13. Pubmed ID: 39532815; DOI: 10.1007/s13577-024-01147-x; PMC: PMC11557646 BRCi028-ABRCi029-ABRCi032-ABRCi033-ABRCi035-A 2024-11-13 2024-11-13 PubMed: 39532815 DOI: 10.1007/s13577-024-01147-x -
Yang Wenke, Wang Shuyue, Yang Ke, Li Yanjun, Guo Zhenglong, Huang Jianmei, Wang Jinming, Liao Shixiu
Transcriptome analyses reveal molecular mechanisms of novel compound heterozygous ACO2 variants causing infantile cerebellar retinal degeneration
Yang Wenke et al. Transcriptome analyses reveal molecular mechanisms of novel compound heterozygous ACO2 variants causing infantile cerebellar retinal degeneration. . 2024-11-12. DOI: 10.3389/fncel.2024.1492048 IISHDOi006-A 2024-11-12 2024-11-12 DOI: 10.3389/fncel.2024.1492048Associated cell lines:
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Scuto Maria, Majzúnová Miroslava, Torcitto Gessica, Antonuzzo Silvia, Rampulla Francesco, Di Fatta Eleonora, Trovato Salinaro Angela
Functional Food Nutrients, Redox Resilience Signaling and Neurosteroids for Brain Health
Scuto Maria et al. Functional Food Nutrients, Redox Resilience Signaling and Neurosteroids for Brain Health. . 2024-11-12. DOI: 10.3390/ijms252212155 SZGJMSi004-A 2024-11-12 2024-11-12 DOI: 10.3390/ijms252212155Associated cell lines:
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Yammine Kathryn M., Abularach Sophia Mirda, Xiong Michael, Kim Seo-yeon, Bikovtseva Agata A., Butty Vincent L., Schiavoni Richard P., Bateman John F., Lamandé Shireen R., Shoulders Matthew D.
Human cartilage model of the precocious osteoarthritis-inducingCOL2A1p.Arg719Cys reveals pathology-driving matrix defects and a failure of the ER proteostasis network to recognize the defective procollagen-II
Yammine Kathryn M. et al. Human cartilage model of the precocious osteoarthritis-inducingCOL2A1p.Arg719Cys reveals pathology-driving matrix defects and a failure of the ER proteostasis network to recognize the defective procollagen-II. . 2024-11-09. DOI: 10.1101/2024.11.07.622468 MCRIi019-AMCRIi019-A-6 2024-11-09 2024-11-09 DOI: 10.1101/2024.11.07.622468Associated cell lines:
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Huang C, Qiu L, Zhou W, Shao C, Wang X, Zhang Q, Chen W, Xiong M, Huang M, Tang M, Zou L, Xu X
A human-induced pluripotent stem cell (iPSC) line (SMUSHi006-A) from an ALS patient carrying a mutation c.1126C > T in the FUS gene
Huang C et al. A human-induced pluripotent stem cell (iPSC) line (SMUSHi006-A) from an ALS patient carrying a mutation c.1126C > T in the FUS gene. . 2024-11-09. Pubmed ID: 39662462; DOI: 10.1016/j.scr.2024.103604 SMUSHi006-A 2024-11-09 2024-11-09 PubMed: 39662462 DOI: 10.1016/j.scr.2024.103604Associated cell lines:
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Begovic Merima, Schneider Luca, Zhou Xiaobo, Hamdani Nazha, Akin Ibrahim, El-Battrawy Ibrahim
The Role of Human-Induced Pluripotent Stem Cells in Studying Cardiac Channelopathies
Begovic Merima et al. The Role of Human-Induced Pluripotent Stem Cells in Studying Cardiac Channelopathies. . 2024-11-08. DOI: 10.3390/ijms252212034 BBANTWi006-ABBANTWi007-A 2024-11-08 2024-11-08 DOI: 10.3390/ijms252212034Associated cell lines:
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Silvestri B, Mochi M, Mawrie D, de Turris V, Colantoni A, Borhy B, Medici M, Anderson EN, Garone MG, Zammerilla CP, Simula M, Ballarino M, Pandey UB, Rosa A
HuD impairs neuromuscular junctions and induces apoptosis in human iPSC and Drosophila ALS models
Silvestri B et al. HuD impairs neuromuscular junctions and induces apoptosis in human iPSC and Drosophila ALS models. . 2024-11-07. Pubmed ID: 39511225; DOI: 10.1038/s41467-024-54004-8; PMC: PMC11544248 WTSIi004-A 2024-11-07 2024-11-07 PubMed: 39511225 DOI: 10.1038/s41467-024-54004-8Associated cell lines:
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Li J, Wiesinger A, Fokkert L, Bakker P, de Vries DK, Tijsen AJ, Pinto YM, Verkerk AO, Christoffels VM, Boink GJJ, Devalla HD
Modeling the atrioventricular conduction axis using human pluripotent stem cell-derived cardiac assembloids
Li J et al. Modeling the atrioventricular conduction axis using human pluripotent stem cell-derived cardiac assembloids. . 2024-11-07. Pubmed ID: 39260368; DOI: 10.1016/j.stem.2024.08.008; PMC: PMC11546832 LUMCi004-A 2024-11-07 2024-11-07 PubMed: 39260368 DOI: 10.1016/j.stem.2024.08.008Associated cell lines:
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Mao YQ, Jahanshahi S, Malty R, Van Ommen DAJ, Wan Y, Morey TM, Chuang SHW, Pavlova V, Ahmed C, Dahal S, Lin F, Mangos M, Nurtanto J, Song Y, Been T, Christie-Holmes N, Gray-Owen SD, Babu M, Wong AP, Batey RA, Attisano L, Cochrane A, Houry WA
Targeting protein homeostasis with small molecules as a strategy for the development of pan-coronavirus antiviral therapies
Mao YQ et al. Targeting protein homeostasis with small molecules as a strategy for the development of pan-coronavirus antiviral therapies. . 2024-11-07. Pubmed ID: 39511285; DOI: 10.1038/s42003-024-07143-z; PMC: PMC11543989 WAe009-A 2024-11-07 2024-11-07 PubMed: 39511285 DOI: 10.1038/s42003-024-07143-zAssociated cell lines:
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Rahimov F, Nieminen P, Kumari P, Juuri E, Nikopensius T, Paraiso K, German J, Karvanen A, Kals M, Elnahas AG, Karjalainen J, Kurki M, Palotie A, FinnGen, Estonian Biobank Research Team, Heliövaara A, Esko T, Jukarainen S, Palta P, Ganna A, Patni AP, Mar D, Bomsztyk K, Mathieu J, Ruohola-Baker H, Visel A, Fakhouri WD, Schutte BC, Cornell RA, Rice DP
High incidence and geographic distribution of cleft palate in Finland are associated with the IRF6 gene
Rahimov F et al. High incidence and geographic distribution of cleft palate in Finland are associated with the IRF6 gene. . 2024-11-06. Pubmed ID: 39500877; DOI: 10.1038/s41467-024-53634-2; PMC: PMC11538390 UCSFi001-A 2024-11-06 2024-11-06 PubMed: 39500877 DOI: 10.1038/s41467-024-53634-2Associated cell lines:
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Kania Evan E., Fenix Aidan, Marciniak Daphnée M., Lin Qiaoyi, Bianchi Sara, Hristov Borislav, Li Shuai, Camplisson Conor K., Fields Rose, Beliveau Brian J., Schweppe Devin K., Noble William S., Ong Shao-En, Bertero Alessandro, Murry Charles E., Shechner David M.
Nascent transcript O-MAP reveals the molecular architecture of a single-locus subnuclear compartment built by RBM20 and theTTNRNA
Kania Evan E. et al. Nascent transcript O-MAP reveals the molecular architecture of a single-locus subnuclear compartment built by RBM20 and theTTNRNA. . 2024-11-06. DOI: 10.1101/2024.11.05.622011 RUESe002-A 2024-11-06 2024-11-06 DOI: 10.1101/2024.11.05.622011Associated cell lines:
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McKinnon Jayden C., Balez Rachelle, Young Reuben S.E., Brown Mikayla L., Lum Jeremy S., Robinson Liam, Belov Mikhail E., Ooi Lezanne, Tortorella Sara, Mitchell Todd W., Ellis Shane R.
MALDI-2-Enabled Oversampling for the Mass Spectrometry Imaging of Metabolites at Single-Cell Resolution
McKinnon Jayden C. et al. MALDI-2-Enabled Oversampling for the Mass Spectrometry Imaging of Metabolites at Single-Cell Resolution. . 2024-11-06. DOI: 10.1021/jasms.4c00241 UOWi005-A 2024-11-06 2024-11-06 DOI: 10.1021/jasms.4c00241Associated cell lines:
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De La Cruz B, Mitra S, He B, Çelik M, Kaminski D, Smedler E, Sterky F.
Efficient Gene-Editing in Human Pluripotent Stem Cells Through Simplified Assembly of Adeno-Associated Viral (AAV) Donor Templates
De La Cruz B et al. Efficient Gene-Editing in Human Pluripotent Stem Cells Through Simplified Assembly of Adeno-Associated Viral (AAV) Donor Templates. . 2024-11-05. WAe009-A 2024-11-05 2024-11-05Associated cell lines:
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Javed Sundas, Fersini Marco, Bernardini Giulia
Unleashing the Power of Induced Pluripotent stem Cells in in vitro Modelling of Lesch-Nyhan Disease
Javed Sundas et al. Unleashing the Power of Induced Pluripotent stem Cells in in vitro Modelling of Lesch-Nyhan Disease. . 2024-11-04. DOI: 10.1007/s12015-024-10821-4 SDQLCHi030-A 2024-11-04 2024-11-04 DOI: 10.1007/s12015-024-10821-4Associated cell lines:
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Chen Chaoxian, Zhang Houan, Qiao Dongxu, Xia Peng, Zhang Yunhao, Dang Wei, Gu Siyong, Yang Yihang
Microstructure and mechanical properties of (Ti, W, Mo, Nb, Ta) (C0.78, N0.22) high entropy cermets with 5–25 wt% Co–Ni binders
Chen Chaoxian et al. Microstructure and mechanical properties of (Ti, W, Mo, Nb, Ta) (C0.78, N0.22) high entropy cermets with 5–25 wt% Co–Ni binders. . 2024-11-00. DOI: 10.1016/j.ceramint.2024.08.090 ZZUNEUi003-A 2024-11-00 2024-11-00 DOI: 10.1016/j.ceramint.2024.08.090Associated cell lines:
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Nuermaimaiti Maierdanjiang, Ishikawa Kei-ichi, Oyama Genko, Nonaka Risa, Shiga Takahiro, Jo Takayuki, Tsunemi Taiji, Nakamura Ryota, Krüger Rejko, Akamatsu Wado, Hattori Nobutaka
Human induced pluripotent stem cell-derived dopaminergic neurons release alpha-synuclein through neuronal activity
Nuermaimaiti Maierdanjiang et al. Human induced pluripotent stem cell-derived dopaminergic neurons release alpha-synuclein through neuronal activity. . 2024-11-00. DOI: 10.1016/j.neures.2024.11.007 HIHDNDi001-AHIHDNDi001-B 2024-11-00 2024-11-00 DOI: 10.1016/j.neures.2024.11.007Associated cell lines:
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Kim D, Lim H, Youn J, Park TE, Kim DS
Scalable production of uniform and mature organoids in a 3D geometrically-engineered permeable membrane
Kim D et al. Scalable production of uniform and mature organoids in a 3D geometrically-engineered permeable membrane. . 2024-10-31. Pubmed ID: 39482314; DOI: 10.1038/s41467-024-53073-z; PMC: PMC11528013 WISCi004-B 2024-10-31 2024-10-31 PubMed: 39482314 DOI: 10.1038/s41467-024-53073-zAssociated cell lines:
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Henke Marie‐Thérèse, Prigione Alessandro, Schuelke Markus
Disease models of Leigh syndrome: From yeast to organoids
Henke Marie‐Thérèse et al. Disease models of Leigh syndrome: From yeast to organoids. . 2024-11-00. DOI: 10.1002/jimd.12804 UOMi001-AUOMi002-AIUFi002-ANTUHi004-A 2024-11-00 2024-11-00 DOI: 10.1002/jimd.12804Associated cell lines:
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Zhuang Mengjie, Zhu Sensen, Su Liping, Liu Li, Ji Min, Xiao Jinling, Guan Yaling, Dai Chenlu, Liu Jingyu, Yang Long, Pu Hongwei
SNTA1 inhibits the PI3K/AKT signaling pathway leading to increased mitochondrial dysfunction and arrhythmia caused by diacetylmorphine
Zhuang Mengjie et al. SNTA1 inhibits the PI3K/AKT signaling pathway leading to increased mitochondrial dysfunction and arrhythmia caused by diacetylmorphine. . 2024-11-00. DOI: 10.1016/j.ecoenv.2024.117212 WAe009-AWAe009-A-50 2024-11-00 2024-11-00 DOI: 10.1016/j.ecoenv.2024.117212Associated cell lines:
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AlAbdi Lama, Maddirevula Sateesh, Aljamal Bayan, Hamid Halima, Almulhim Aisha, Hashem Mais O., Algoos Yusra, Alqahtani Mashael, Albaloshi Shahad, Alghamdi Mohammed, Alduaylij Mohammed, Shamseldin Hanan E., Nadeef Seba, Patel Nisha, Abdulwahab Firdous, Abouyousef Omar, Alshidi Tarfa, Jaafar Amal, Abouelhoda Mohamed, Alhazzani Adel, Alfares Ahmed, Qudair Ahmad, Alsulaiman Ahood, Alhashem Amal, Khan Arif O., Chedrawi Aziza, Alebdi Basel, AlAjlan Fahad, Alotaibi Fawaz, Alzaidan Hamad, Banjar Hanaa, Abdelraouf Hanem, Alkuraya Hisham, Abumansour Iman, Alfayez Khowlah, Tulbah Maha, Alowain Mohammed, Alqahtani Mohammed, El-Kalioby Mohammed, Shboul Mohammad, Sulaiman Raashda, Al Tala Saed, Khan Sameena, Coskun Serdar, Mrouge Sobaihi, Alenazi Walaa, Rahbeeni Zuhair, Alkuraya Fowzan S.
Arab founder variants: Contributions to clinical genomics and precision medicine
AlAbdi Lama et al. Arab founder variants: Contributions to clinical genomics and precision medicine. . 2024-11-00. DOI: 10.1016/j.medj.2024.10.005 KAUSTi011-AKAUSTi011-B 2024-11-00 2024-11-00 DOI: 10.1016/j.medj.2024.10.005Associated cell lines:
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Peters Marijn C., Zaldumbide Arnaud, Groeneveld Esmee J., Rabelink Martijn J.W.E., Peerlings Janneke H., van den Bogaerdt Antoon, Bouten Carlijn V.C., Hoeben Rob C., Goumans Marie-Jose, van Wijk Abraham
Immune Shielding of Human Heart Valves
Peters Marijn C. et al. Immune Shielding of Human Heart Valves. . 2024-11-00. DOI: 10.1016/j.jacbts.2024.07.003 MUSIi001-AMUSIi001-A-2 2024-11-00 2024-11-00 DOI: 10.1016/j.jacbts.2024.07.003Associated cell lines:
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Kuroda Yukiko, Uehara Takeshi, Enomoto Yumi, Naruto Takuya, Matsumura Nozomi, Kurosawa Kenji
GPC4 truncating variant associated with Keipert syndrome and lacrimal punctal agenesisGPC4 truncating variant associated with Keipert syndrome and lacrimal punctal agenesis. . 2024-11-00. DOI: 10.1002/ajmg.a.63799 ATCi002-A 2024-11-00 2024-11-00 DOI: 10.1002/ajmg.a.63799Associated cell lines:
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Xie Changning, Kessi Miriam, Yin Fei, Peng Jing
Roles of KCNA2 in Neurological Diseases: from Physiology to Pathology
Xie Changning et al. Roles of KCNA2 in Neurological Diseases: from Physiology to Pathology. . 2024-11-00. DOI: 10.1007/s12035-024-04120-9 HIHDNEi002-AHIHDNEi003-ANUIGi052-ANUIGi052-BNUIGi052-C 2024-11-00 2024-11-00 DOI: 10.1007/s12035-024-04120-9Associated cell lines:
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Pandit A, Indurkar A, Locs J, Haugen HJ, Loca D
Calcium Phosphates: A Key to Next-Generation In Vitro Bone Modeling
Pandit A et al. Calcium Phosphates: A Key to Next-Generation In Vitro Bone Modeling. . 2024-11-00. Pubmed ID: 39175382; DOI: 10.1002/adhm.202401307; PMC: PMC11582516 GZHMCi003-A 2024-11-00 2024-11-00 PubMed: 39175382 DOI: 10.1002/adhm.202401307Associated cell lines:
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Raabe J, Wittig I, Laurette P, Stathopoulou K, Brand T, Schulze T, Klampe B, Orthey E, Cabrera-Orefice A, Meisterknecht J, Thiemann E, Laufer SD, Shibamiya A, Reinsch M, Fuchs S, Kaiser J, Yang J, Zehr S, Wrona KM, Lorenz K, Lukowski R, Hansen A, Gilsbach R, Brandes RP, Ulmer BM, Eschenhagen T, Cuello F
Physioxia rewires mitochondrial complex composition to protect stem cell viability
Raabe J et al. Physioxia rewires mitochondrial complex composition to protect stem cell viability. . 2024-11-00. Pubmed ID: 39341035; DOI: 10.1016/j.redox.2024.103352; PMC: PMC11466565 UKEi001-A 2024-11-00 2024-11-00 PubMed: 39341035 DOI: 10.1016/j.redox.2024.103352Associated cell lines:
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Liu W. Q., Zhu L. F., Zhang T., Zeng S. X., Hu L.
Bioinformatic Analysis of the Molecular Pathways of ATRX and XIST in X Chromosome Inactivation
Liu W. Q. et al. Bioinformatic Analysis of the Molecular Pathways of ATRX and XIST in X Chromosome Inactivation. . 2024-11-00. DOI: 10.1134/s1022795424701138 GZHMUi001-A 2024-11-00 2024-11-00 DOI: 10.1134/s1022795424701138Associated cell lines:
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Dya German A., Lebedeva Olga S., Gushchevarov Daniil A., Volovikov Egor A., Belikova Lilia D., Kopylova Irina V., Postnikov Alexander B., Artemieva Marina M., Medvedeva Natalia A., Lagarkova Maria A., Katrukha Alexey G., Serebryanaya Daria V.
Specific cleavage of IGFBP-4 by papp-a in nervous tissue
Dya German A. et al. Specific cleavage of IGFBP-4 by papp-a in nervous tissue. . 2024-11-00. DOI: 10.1016/j.bbrc.2024.150655 RCPCMi007-ARCPCMi007-A-1 2024-11-00 2024-11-00 DOI: 10.1016/j.bbrc.2024.150655Associated cell lines:
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Yang M, You D, Liu G, Lu Y, Yang G, O'Brien T, Henshall DC, Hardiman O, Cai L, Liu M, Shen S
Polyethyleneimine facilitates the growth and electrophysiological characterization of iPSC-derived motor neurons
Yang M et al. Polyethyleneimine facilitates the growth and electrophysiological characterization of iPSC-derived motor neurons. . 2024-10-30. Pubmed ID: 39478194; DOI: 10.1038/s41598-024-77710-1; PMC: PMC11525838 NUIGi043-ANUIGi043-BNUIGi043-CNUIGi044-ANUIGi044-BNUIGi044-CNUIGi049-ANUIGi050-ANUIGi051-A 2024-10-30 2024-10-30 PubMed: 39478194 DOI: 10.1038/s41598-024-77710-1Associated cell lines:
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Wolnik Jan, Adamska Patrycja, Oleksy Aleksandra, Sanetra Anna Magdalena, Palus-Chramiec Katarzyna, Lewandowski Marian Henryk, Dulak Józef, Biniecka Monika
A novel 3D cardiac microtissue model for investigation of cardiovascular complications in rheumatoid arthritis
Wolnik Jan et al. A novel 3D cardiac microtissue model for investigation of cardiovascular complications in rheumatoid arthritis. . 2024-10-29. DOI: 10.1186/s13287-024-03956-1 DMBi003-ADMBi004-A 2024-10-29 2024-10-29 DOI: 10.1186/s13287-024-03956-1 -
Langlois J, Lange S, Ebeling M, Macnair W, Schmucki R, Li C, DeGeer J, Sudharshan TJJ, Yong VW, Shen YA, Harp C, Collin L, Keaney J
Fenebrutinib, a Bruton's tyrosine kinase inhibitor, blocks distinct human microglial signaling pathways
Langlois J et al. Fenebrutinib, a Bruton's tyrosine kinase inhibitor, blocks distinct human microglial signaling pathways. . 2024-10-27. Pubmed ID: 39465429; DOI: 10.1186/s12974-024-03267-5; PMC: PMC11514909 BIONi037-A 2024-10-27 2024-10-27 PubMed: 39465429 DOI: 10.1186/s12974-024-03267-5Associated cell lines:
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Li Lei, Zhao Zijuan, Liu Zihao, Tang Yuquan, Yang Tan, Gong Nailin, Liao Bing, Long Yang, Nie Yongmei, Yu Fengxu
Identification of the optimal reference genes for atrial fibrillation model established by iPSC-derived atrial myocytes
Li Lei et al. Identification of the optimal reference genes for atrial fibrillation model established by iPSC-derived atrial myocytes. . 2024-10-25. DOI: 10.1186/s12864-024-10922-x CSCRi006-A 2024-10-25 2024-10-25 DOI: 10.1186/s12864-024-10922-xAssociated cell lines:
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Tong X, Poramba-Liyanage DW, van Hoolwerff M, Riemers FM, Montilla-Rojo J, Warin J, Salvatori D, Camus A, Meulenbelt I, Ramos YFM, Geijsen N, Tryfonidou MA, Shang P
Isolation and tracing of matrix-producing notochordal and chondrocyte cells using ACAN-2A-mScarlet reporter human iPSC lines
Tong X et al. Isolation and tracing of matrix-producing notochordal and chondrocyte cells using ACAN-2A-mScarlet reporter human iPSC lines. . 2024-10-25. Pubmed ID: 39441923; DOI: 10.1126/sciadv.adp3170; PMC: PMC11498221 TMOi001-AMCRIi001-AMCRIi001-A-2TMOi001-A-14TMOi001-A-15 2024-10-25 2024-10-25 PubMed: 39441923 DOI: 10.1126/sciadv.adp3170Associated cell lines:
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Wang Brian Xiangzhi
Investigating Inherited Heart Diseases Using Human Induced Pluripotent Stem Cell-Based Models
Wang Brian Xiangzhi. Investigating Inherited Heart Diseases Using Human Induced Pluripotent Stem Cell-Based Models. . 2024-10-25. DOI: 10.3390/life14111370 ZZUNEUi020-A 2024-10-25 2024-10-25 DOI: 10.3390/life14111370Associated cell lines:
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Semenova P. I., Panova A. V., Sopova J. V., Krasnova O. A., Turilova V. I., Yakovleva T. K., Kulikova K. S., Petrova D. A., Kiselev S. L., Neganova I. E.
Generation of CRISPR/Cas9 modified human iPSC line with correction of heterozygous mutation in exon 6 of the CaSR gene
Semenova P. I. et al. Generation of CRISPR/Cas9 modified human iPSC line with correction of heterozygous mutation in exon 6 of the CaSR gene. . 2024-10-24. DOI: 10.1007/s13577-024-01135-1 CSSi015-A 2024-10-24 2024-10-24 DOI: 10.1007/s13577-024-01135-1Associated cell lines:
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Borisch Carla, Thum Thomas, Bär Christian, Hoepfner Jeannine
Human in vitro models for Fabry disease: new paths for unravelling disease mechanisms and therapies
Borisch Carla et al. Human in vitro models for Fabry disease: new paths for unravelling disease mechanisms and therapies. . 2024-10-24. DOI: 10.1186/s12967-024-05756-w MHHi029-A 2024-10-24 2024-10-24 DOI: 10.1186/s12967-024-05756-wAssociated cell lines:
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Ging K, Frick L, Schlachetzki J, Armani A, Zhu Y, Gilormini PA, Dhingra A, Böck D, Marques A, Deen M, Chen X, Serdiuk T, Trevisan C, Sellitto S, Pisano C, Glass CK, Heutink P, Yin JA, Vocadlo DJ, Aguzzi A
Direct and indirect regulation of β-glucocerebrosidase by the transcription factors USF2 and ONECUT2
Ging K et al. Direct and indirect regulation of β-glucocerebrosidase by the transcription factors USF2 and ONECUT2. . 2024-10-22. Pubmed ID: 39438499; DOI: 10.1038/s41531-024-00819-7; PMC: PMC11496744 UOXFi001-B 2024-10-22 2024-10-22 PubMed: 39438499 DOI: 10.1038/s41531-024-00819-7Associated cell lines:
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Liu S, Yang N, Yan Y, Wang S, Chen J, Wang Y, Gan X, Zhou J, Xie G, Wang H, Huang T, Ji W, Wang Z, Si W
An accelerated Parkinson's disease monkey model using AAV-α-synuclein plus poly(ADP-ribose)
Liu S et al. An accelerated Parkinson's disease monkey model using AAV-α-synuclein plus poly(ADP-ribose). . 2024-10-21. Pubmed ID: 39413778; DOI: 10.1016/j.crmeth.2024.100876; PMC: PMC11573744 WAe009-A 2024-10-21 2024-10-21 PubMed: 39413778 DOI: 10.1016/j.crmeth.2024.100876Associated cell lines:
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Rosochowicz MA, Lach MS, Richter M, Jagiełło I, Suchorska WM, Trzeciak T
The iPSC secretome is beneficial for in vitro propagation of primary osteoarthritic chondrocytes cell lines
Rosochowicz MA et al. The iPSC secretome is beneficial for in vitro propagation of primary osteoarthritic chondrocytes cell lines. . 2024-10-20. Pubmed ID: 39003867; DOI: 10.1016/j.bbrc.2024.150392 GPCCi001-A 2024-10-20 2024-10-20 PubMed: 39003867 DOI: 10.1016/j.bbrc.2024.150392Associated cell lines:
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Vicente Pedro, Almeida Joana I., Crespo Inês E., Virgolini Nikolaus, Isidro Inês A., Calleja-Cervantes Maria Eréndira, Rodriguez-Madoz Juan R., Prosper Felipe, Alves Paula M., Serra Margarida
Oxygen control in bioreactor drives high yield production of functional hiPSC-like hepatocytes for advanced liver disease modelling
Vicente Pedro et al. Oxygen control in bioreactor drives high yield production of functional hiPSC-like hepatocytes for advanced liver disease modelling. . 2024-10-19. DOI: 10.1038/s41598-024-75582-z CIMAi001-A 2024-10-19 2024-10-19 DOI: 10.1038/s41598-024-75582-zAssociated cell lines:
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Trinh J, Schaake S, Gabbert C, Lüth T, Cowley SA, Fienemann A, Ullrich KK, Klein C, Seibler P
Optical genome mapping of structural variants in Parkinson's disease-related induced pluripotent stem cells
Trinh J et al. Optical genome mapping of structural variants in Parkinson's disease-related induced pluripotent stem cells. . 2024-10-19. Pubmed ID: 39425080; DOI: 10.1186/s12864-024-10902-1; PMC: PMC11490025 STBCi024-CSTBCi057-ASTBCi102-A 2024-10-19 2024-10-19 PubMed: 39425080 DOI: 10.1186/s12864-024-10902-1Associated cell lines:
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Ewoldt JK, Wang MC, McLellan MA, Cloonan PE, Chopra A, Gorham J, Li L, DeLaughter DM, Gao X, Lee JH, Willcox JAL, Layton O, Luu RJ, Toepfer CN, Eyckmans J, Seidman CE, Seidman JG, Chen CS
Hypertrophic cardiomyopathy-associated mutations drive stromal activation via EGFR-mediated paracrine signaling
Ewoldt JK et al. Hypertrophic cardiomyopathy-associated mutations drive stromal activation via EGFR-mediated paracrine signaling. . 2024-10-18. Pubmed ID: 39413182; DOI: 10.1126/sciadv.adi6927; PMC: PMC11482324 SCVIi001-A 2024-10-18 2024-10-18 PubMed: 39413182 DOI: 10.1126/sciadv.adi6927Associated cell lines:
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Yang HS, Zheng YX, Bai X, He XY, Wang TH
Application prospects of urine-derived stem cells in neurological and musculoskeletal diseases
Yang HS et al. Application prospects of urine-derived stem cells in neurological and musculoskeletal diseases. . 2024-10-18. Pubmed ID: 39473520; DOI: 10.5312/wjo.v15.i10.918; PMC: PMC11514553 MUSIi005-ACSUASOi001-ASDQLCHi008-ACSUASOi006-ASMBCi009-AHHUUKDi011-AHHUUKDi012-A 2024-10-18 2024-10-18 PubMed: 39473520 DOI: 10.5312/wjo.v15.i10.918Associated cell lines:
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Lee Yoo Jin, Jo Dong Hyun
Retinal Organoids from Induced Pluripotent Stem Cells of Patients with Inherited Retinal Diseases: A Systematic Review
Lee Yoo Jin et al. Retinal Organoids from Induced Pluripotent Stem Cells of Patients with Inherited Retinal Diseases: A Systematic Review. . 2024-10-18. DOI: 10.1007/s12015-024-10802-7 ZOCi001-ALEIi019-A 2024-10-18 2024-10-18 DOI: 10.1007/s12015-024-10802-7 -
Ge Ning, Li Rui, Liu Min, Xia Wenxin, O'Brien Stephen T., McInerney Veronica, Galvin Joseph, Ward Deirdre, McGorrian Catherine, O'Brien Timothy, Shen Sanbing, Prendiville Terence W.
Defining Cardiomyocyte Repolarization Response to Pharmacotherapy in Long‐QT Syndrome Type 3
Ge Ning et al. Defining Cardiomyocyte Repolarization Response to Pharmacotherapy in Long‐QT Syndrome Type 3. . 2024-10-15. DOI: 10.1161/jaha.124.034690 NUIGi038-ANUIGi038-B 2024-10-15 2024-10-15 DOI: 10.1161/jaha.124.034690Associated cell lines:
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Cotta GC, Teixeira Dos Santos RC, Costa GMJ, Lacerda SMDSN
Reporter Alleles in hiPSCs: Visual Cues on Development and Disease
Cotta GC et al. Reporter Alleles in hiPSCs: Visual Cues on Development and Disease. . 2024-10-13. Pubmed ID: 39456792; DOI: 10.3390/ijms252011009; PMC: PMC11507014 SNUe003-AHMGUi001-AMHHi007-AMHHi007-A-1MCRIi001-AKSCBi005-AKSCBi005-A-1GIBHi002-AGIBHi002-A-2HMGUi001-A-4MCRIi001-A-3MCRIi001-A-4SNUe003-A-2 2024-10-13 2024-10-13 PubMed: 39456792 DOI: 10.3390/ijms252011009Associated cell lines:
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Fischer Inbar, Shohat Sophie, Leichtmann-Bardoogo Yael, Nayak Ritu, Wiener Gal, Rosh Idan, Shemen Aviram, Tripathi Utkarsh, Rokach May, Bar Ela, Hussein Yara, Castro Ana Carolina, Chen Gal, Soffer Adi, Schokoroy-Trangle Sari, Elad-Sfadia Galit, Assaf Yaniv, Schroeder Avi, Monteiro Patricia, Stern Shani, Maoz Ben M., Barak Boaz
Shank3 mutation impairs glutamate signaling and myelination in ASD mouse model and human iPSC-derived OPCs
Fischer Inbar et al. Shank3 mutation impairs glutamate signaling and myelination in ASD mouse model and human iPSC-derived OPCs. . 2024-10-11. DOI: 10.1126/sciadv.adl4573 UOHi002-AUOHi003-A 2024-10-11 2024-10-11 DOI: 10.1126/sciadv.adl4573 -
Pietsch N, Chen CY, Kupsch S, Bacmeister L, Geertz B, Herrera-Rivero M, Siebels B, Voß H, Krämer E, Braren I, Westermann D, Schlüter H, Mearini G, Schlossarek S, van der Velden J, Caporizzo MA, Lindner D, Prosser BL, Carrier L
Chronic Activation of Tubulin Tyrosination Improves Heart Function
Pietsch N et al. Chronic Activation of Tubulin Tyrosination Improves Heart Function. . 2024-10-11. Pubmed ID: 39279670; DOI: 10.1161/circresaha.124.324387; PMC: PMC11465905 UKEi070-A 2024-10-11 2024-10-11 PubMed: 39279670 DOI: 10.1161/circresaha.124.324387Associated cell lines:
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Sugie Kazuma, Nishino Ichizo
History and Perspective of LAMP-2 Deficiency (Danon Disease)
Sugie Kazuma et al. History and Perspective of LAMP-2 Deficiency (Danon Disease). . 2024-10-09. DOI: 10.3390/biom14101272 ZZUNEUi020-A 2024-10-09 2024-10-09 DOI: 10.3390/biom14101272Associated cell lines:
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Villafranco Javier, Martínez-Ramírez Gabriela, Magaña-Maldonado Roxana, González-Ruvalcaba Anna Paola, López-Ornelas Adolfo, Velasco Iván, Becerril-Villanueva Enrique, Pavón Lenin, Estudillo Enrique, Pérez-Sánchez Gilberto
The use of induced pluripotent stem cells as a platform for the study of depression
Villafranco Javier et al. The use of induced pluripotent stem cells as a platform for the study of depression. . 2024-10-09. DOI: 10.3389/fpsyt.2024.1470642 SZGJMSi004-A 2024-10-09 2024-10-09 DOI: 10.3389/fpsyt.2024.1470642Associated cell lines:
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Chang Y, Bai R, Zhang Y, Lu WJ, Ma S, Zhu M, Lan F, Jiang Y
SMYD1 modulates the proliferation of multipotent cardiac progenitor cells derived from human pluripotent stem cells during myocardial differentiation through GSK3β/β-catenin&ERK signaling
Chang Y et al. SMYD1 modulates the proliferation of multipotent cardiac progenitor cells derived from human pluripotent stem cells during myocardial differentiation through GSK3β/β-catenin&ERK signaling. . 2024-10-08. Pubmed ID: 39380045; DOI: 10.1186/s13287-024-03899-7; PMC: PMC11462858 WAe009-AWAe009-A-94 2024-10-08 2024-10-08 PubMed: 39380045 DOI: 10.1186/s13287-024-03899-7Associated cell lines:
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Wells CA, Guhr A, Bairoch A, Chen Y, Hu M, Löser P, Ludwig TE, Mah N, Mueller SC, Seiler Wulczyn AEM, Seltmann S, Rossbach B, Kurtz A
Guidelines for managing and using the digital phenotypes of pluripotent stem cell lines
Wells CA et al. Guidelines for managing and using the digital phenotypes of pluripotent stem cell lines. . 2024-10-08. Pubmed ID: 39332404; DOI: 10.1016/j.stemcr.2024.08.009; PMC: PMC11561460 WAe009-A 2024-10-08 2024-10-08 PubMed: 39332404 DOI: 10.1016/j.stemcr.2024.08.009Associated cell lines:
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Tang Fan, Dong Tao, Zhou Chengqian, Deng Leon, Liu Hans B., Wang Wenshen, Liu Guanshu, Ying Mingyao, Li Pan P.
Genetically engineered human induced pluripotent stem cells for the production of brain-targeting extracellular vesicles
Tang Fan et al. Genetically engineered human induced pluripotent stem cells for the production of brain-targeting extracellular vesicles. . 2024-10-08. DOI: 10.1186/s13287-024-03955-2 JHUi003-A 2024-10-08 2024-10-08 DOI: 10.1186/s13287-024-03955-2Associated cell lines:
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Zheng Yiting, Chen Jing
Voltage-gated potassium channels and genetic epilepsy
Zheng Yiting et al. Voltage-gated potassium channels and genetic epilepsy. . 2024-10-07. DOI: 10.3389/fneur.2024.1466075 GZHMCi001-AGZHMCi001-B 2024-10-07 2024-10-07 DOI: 10.3389/fneur.2024.1466075Associated cell lines:
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Baldé H, Geurts B, Fischer HT, Menelik-Obbarius S, Kaba I, Merhi V, Stein K, Diaconu V, Bahr T, Weishaar H, Delamou A, Mbawah AK, El-Bcheraoui C
Responding to fluctuations in public and community trust and health seeking behaviour during the COVID-19 pandemic: a qualitative study of national decision-makers' perspectives in Guinea and Sierra Leone
Baldé H et al. Responding to fluctuations in public and community trust and health seeking behaviour during the COVID-19 pandemic: a qualitative study of national decision-makers' perspectives in Guinea and Sierra Leone. . 2024-10-04. Pubmed ID: 39367378; DOI: 10.1186/s12889-024-20181-w; PMC: PMC11452948 KIi002-A 2024-10-04 2024-10-04 PubMed: 39367378 DOI: 10.1186/s12889-024-20181-wAssociated cell lines:
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Janpipatkul K, Sutjarit N, Tangprasittipap A, Chaiamarit T, Innachai P, Suksen K, Chokpanuwat T, Tim-Aroon T, Anurathapan U, Jearawiriyapaisarn N, Tubsuwan A, Bowornpinyo S, Asavapanumas N, Chairoungdua A, Bhukhai K, Hongeng S
Therapeutic delivery of recombinant glucocerebrosidase enzyme-containing extracellular vesicles to human cells from Gaucher disease patients
Janpipatkul K et al. Therapeutic delivery of recombinant glucocerebrosidase enzyme-containing extracellular vesicles to human cells from Gaucher disease patients. . 2024-10-02. Pubmed ID: 39358794; DOI: 10.1186/s13023-024-03376-7; PMC: PMC11445852 MUi019-AMUi030-AMUi031-A 2024-10-02 2024-10-02 PubMed: 39358794 DOI: 10.1186/s13023-024-03376-7 -
Baggiani Matteo, Damiani Devid, Privitera Flavia, Della Vecchia Stefania, Tessa Alessandra, Santorelli Filippo Maria
Generation and Characterization of hiPS Lines from Three Patients Affected by Different Forms of HPDL-Related Neurological Disorders
Baggiani Matteo et al. Generation and Characterization of hiPS Lines from Three Patients Affected by Different Forms of HPDL-Related Neurological Disorders. . 2024-10-02. DOI: 10.3390/ijms251910614 CSSi016-A 2024-10-02 2024-10-02 DOI: 10.3390/ijms251910614Associated cell lines:
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Almeida Zaida L., Vaz Daniela C., Brito Rui M. M.
Transthyretin mutagenesis: impact on amyloidogenesis and disease
Almeida Zaida L. et al. Transthyretin mutagenesis: impact on amyloidogenesis and disease. . 2024-10-02. DOI: 10.1080/10408363.2024.2350379 PUMCHi004-A 2024-10-02 2024-10-02 DOI: 10.1080/10408363.2024.2350379Associated cell lines:
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van de Weijer ML, Samanta K, Sergejevs N, Jiang L, Dueñas ME, Heunis T, Huang TY, Kaufman RJ, Trost M, Sanyal S, Cowley SA, Carvalho P
Tapasin assembly surveillance by the RNF185/Membralin ubiquitin ligase complex regulates MHC-I surface expression
van de Weijer ML et al. Tapasin assembly surveillance by the RNF185/Membralin ubiquitin ligase complex regulates MHC-I surface expression. . 2024-10-01. Pubmed ID: 39353943; DOI: 10.1038/s41467-024-52772-x; PMC: PMC11445256 STBCi026-A 2024-10-01 2024-10-01 PubMed: 39353943 DOI: 10.1038/s41467-024-52772-xAssociated cell lines:
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Vasilyeva Tatyana, Kadyshev Vitaly, Khalanskaya Olga, Kuznetsova Svetlana, Ionova Sofya, Marakhonov Andrey, Zinchenko Rena
Clinical and Molecular Findings in Patients with Knobloch Syndrome 1: Case Series Report
Vasilyeva Tatyana et al. Clinical and Molecular Findings in Patients with Knobloch Syndrome 1: Case Series Report. . 2024-10-01. DOI: 10.3390/genes15101295 ZSZOCi001-A 2024-10-01 2024-10-01 DOI: 10.3390/genes15101295Associated cell lines:
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Peng J.
Update of generation and application of skin organoids
Peng J.. Update of generation and application of skin organoids. . 2024-10-01. DOI: 10.12144/zgmfskin202410749 RCMGi004-AWAe009-A-82RCMGi008-A 2024-10-01 2024-10-01 DOI: 10.12144/zgmfskin202410749Associated cell lines:
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Bai L.
Update of the treatment for primary cutanious amyloidosis
Bai L.. Update of the treatment for primary cutanious amyloidosis. . 2024-10-01. DOI: 10.12144/zgmfskin202410744 WAe009-A-82 2024-10-01 2024-10-01 DOI: 10.12144/zgmfskin202410744Associated cell lines:
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Chi H, Qu B, Prawira A, Richardt T, Maurer L, Hu J, Fu RM, Lempp FA, Zhang Z, Grimm D, Wu X, Urban S, Dao Thi VL
An hepatitis B and D virus infection model using human pluripotent stem cell-derived hepatocytes
Chi H et al. An hepatitis B and D virus infection model using human pluripotent stem cell-derived hepatocytes. . 2024-10-00. Pubmed ID: 39232200; DOI: 10.1038/s44319-024-00236-0; PMC: PMC11466959 WAe009-A 2024-10-00 2024-10-00 PubMed: 39232200 DOI: 10.1038/s44319-024-00236-0Associated cell lines:
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Sareen N, Srivastava A, Mittal I, Shah AH, Dhingra S
Establishment of a new human iPSC cell line (UOMi012-A) from a patient with congenital heart defect who has undergone Fontan procedure
Sareen N et al. Establishment of a new human iPSC cell line (UOMi012-A) from a patient with congenital heart defect who has undergone Fontan procedure. . 2024-10-00. Pubmed ID: 39089181; DOI: 10.1016/j.scr.2024.103509 UOMi006-AUOMi008-AUOMi012-A 2024-10-00 2024-10-00 PubMed: 39089181 DOI: 10.1016/j.scr.2024.103509 -
Shishkova Daria K., Frolov Alexey V., Markova Victoria E., Markova Yulia O., Lazebnaya Anastasia I., Kutikhin Anton G.
IMPROVING METHODOLOGY OF ENDOTHELIAL CELL RESEARCH: SYNOPSIS AND PROSPECTS
Shishkova Daria K. et al. IMPROVING METHODOLOGY OF ENDOTHELIAL CELL RESEARCH: SYNOPSIS AND PROSPECTS. . 2024-09-30. DOI: 10.17802/2306-1278-2024-13-3-118-129 ICGi021-AICGi022-AICGi036-AICGi037-AICGi038-A 2024-09-30 2024-09-30 DOI: 10.17802/2306-1278-2024-13-3-118-129 -
Alwohoush Enas, Ismail Mohammad A., Al-Kurdi Ban, Barham Raghda, Al Hadidi Sabal, Awidi Abdalla, Ababneh Nidaa A.
Effect of hypoxia on proliferation and differentiation of induced pluripotent stem cell-derived mesenchymal stem cells
Alwohoush Enas et al. Effect of hypoxia on proliferation and differentiation of induced pluripotent stem cell-derived mesenchymal stem cells. . 2024-10-00. DOI: 10.1016/j.heliyon.2024.e38857 JUCTCi010-A 2024-10-00 2024-10-00 DOI: 10.1016/j.heliyon.2024.e38857Associated cell lines:
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Oh JY, Yoo DH, Im YS, Kim YO
Generation and characterization of a human iPSC line expressing EGFP-tagged CDH1, KSCBi002-A-3
Oh JY et al. Generation and characterization of a human iPSC line expressing EGFP-tagged CDH1, KSCBi002-A-3. . 2024-10-00. Pubmed ID: 39121651; DOI: 10.1016/j.scr.2024.103510 KSCBi002-AKSCBi002-A-3 2024-10-00 2024-10-00 PubMed: 39121651 DOI: 10.1016/j.scr.2024.103510Associated cell lines:
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Hanley M, Alonzo M, Ye S, Yu Y, Contreras J, Hayden J, Garg V, Zhao MT
Characterization of an induced pluripotent stem cell line (NCHi013-A) from a 5-year-old male with pulmonary atresia with intact ventricular septum and a biventricular repair
Hanley M et al. Characterization of an induced pluripotent stem cell line (NCHi013-A) from a 5-year-old male with pulmonary atresia with intact ventricular septum and a biventricular repair. . 2024-10-00. Pubmed ID: 39121650; DOI: 10.1016/j.scr.2024.103526; PMC: PMC11404849 NCHi013-A 2024-10-00 2024-10-00 PubMed: 39121650 DOI: 10.1016/j.scr.2024.103526Associated cell lines:
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Ahmad I, Kapoor H, Kumar Srivastava A, Faruq M
Generation and characterization of human-derived induced pluripotent stem cell line (IGIBi010-A) from a patient with neurodegenerative disease phenotype carrying mutation in SQSTM1/p62 gene
Ahmad I et al. Generation and characterization of human-derived induced pluripotent stem cell line (IGIBi010-A) from a patient with neurodegenerative disease phenotype carrying mutation in SQSTM1/p62 gene. . 2024-10-00. Pubmed ID: 39126919; DOI: 10.1016/j.scr.2024.103520 IGIBi005-AIGIBi006-AIGIBi008-AIGIBi010-A 2024-10-00 2024-10-00 PubMed: 39126919 DOI: 10.1016/j.scr.2024.103520Associated cell lines:
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Joseph B, Varea I, Emmerich K, Manohar-Sindhu S, Zou J, Friend K, Sipwoli C, Tang X, Yang D, de Jesus Rasheed AA, Goldbach-Mansky R, Boehm M
Establishment of a human induced pluripotent stem cell line (NIHTVBi031-A) derived from a COPA syndrome patient with a heterozygous p.Ala239Pro mutation
Joseph B et al. Establishment of a human induced pluripotent stem cell line (NIHTVBi031-A) derived from a COPA syndrome patient with a heterozygous p.Ala239Pro mutation. . 2024-10-00. Pubmed ID: 39110999; DOI: 10.1016/j.scr.2024.103504; PMC: PMC11426554 NHLBIi001-ANHLBIi001-BNIHTVBi031-A 2024-10-00 2024-10-00 PubMed: 39110999 DOI: 10.1016/j.scr.2024.103504Associated cell lines:
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Alsalloum A, Shefer K, Bogdanov P, Mingaleva N, Kim A, Feoktistova S, Mityaeva O, Volchkov P
Establishment of a human induced pluripotent stem cell line (ABi004-A) carrying a compound heterozygous mutation in the KCNV2 gene
Alsalloum A et al. Establishment of a human induced pluripotent stem cell line (ABi004-A) carrying a compound heterozygous mutation in the KCNV2 gene. . 2024-10-00. Pubmed ID: 39083856; DOI: 10.1016/j.scr.2024.103512 ABi001-AABi002-AABi004-A 2024-10-00 2024-10-00 PubMed: 39083856 DOI: 10.1016/j.scr.2024.103512 -
Jiang C, Huang W, Zhou Y, Wang J, Lei H, Niu Y, Zhou R, Zhang Y
Generating a human induced pluripotent stem cell line (XACHi018-A) from a Timothy syndrome infant carrying heterozygous CACNA1C c.1216G>A (p.G406R) mutation
Jiang C et al. Generating a human induced pluripotent stem cell line (XACHi018-A) from a Timothy syndrome infant carrying heterozygous CACNA1C c.1216G>A (p.G406R) mutation. . 2024-10-00. Pubmed ID: 39079396; DOI: 10.1016/j.scr.2024.103513 XACHi004-AXACHi018-A 2024-10-00 2024-10-00 PubMed: 39079396 DOI: 10.1016/j.scr.2024.103513Associated cell lines:
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Bianchini L, Sieber L, Hammad R, Schäfer R, Kutscher LM
Generation of two isogenic patient-derived human-induced pluripotent stem cell clones with 6q27 deletion
Bianchini L et al. Generation of two isogenic patient-derived human-induced pluripotent stem cell clones with 6q27 deletion. . 2024-10-00. Pubmed ID: 39106599; DOI: 10.1016/j.scr.2024.103524 DKFZi001-ADKFZi001-B 2024-10-00 2024-10-00 PubMed: 39106599 DOI: 10.1016/j.scr.2024.103524Associated cell lines:
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Varea I, Joseph B, Emmerich K, Manohar-Sindhu S, Zou J, Friend K, Tang X, Yang D, de Jesus Rasheed AA, Goldbach-Mansky R, Boehm M
Human induced pluripotent stem cells (NIHTVBi029-A and NIHTVBi030-A) generated from two patients with a heterozygous mutation in the CDC42 gene
Varea I et al. Human induced pluripotent stem cells (NIHTVBi029-A and NIHTVBi030-A) generated from two patients with a heterozygous mutation in the CDC42 gene. . 2024-10-00. Pubmed ID: 39106600; DOI: 10.1016/j.scr.2024.103517; PMC: PMC11395911 NHLBIi001-ANHLBIi001-BNIHTVBi029-ANIHTVBi030-A 2024-10-00 2024-10-00 PubMed: 39106600 DOI: 10.1016/j.scr.2024.103517Associated cell lines:
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Lim SW, Lee KI, Cui S, Fang X, Shin YJ, Lee H, Lee JY, Chung BH, Yang CW
Generation of green fluorescent protein reporter knock-in iPSC line at the 3'UTR region of the KLOTHO locus
Lim SW et al. Generation of green fluorescent protein reporter knock-in iPSC line at the 3'UTR region of the KLOTHO locus. . 2024-10-00. Pubmed ID: 39111000; DOI: 10.1016/j.scr.2024.103499 UCSFi001-A-78 2024-10-00 2024-10-00 PubMed: 39111000 DOI: 10.1016/j.scr.2024.103499Associated cell lines:
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Kelters Ilse R., Verbueken Devin, Beekink Tess, Van Laake Linda W., Sluijter Joost P.G., Maas Renee G.C., Buikema Jan W.
Generation of human induced pluripotent stem cell (hiPSC) lines derived from three patients carrying the pathogenic CRYAB (A527G) mutation and one non-carrier family member
Kelters Ilse R. et al. Generation of human induced pluripotent stem cell (hiPSC) lines derived from three patients carrying the pathogenic CRYAB (A527G) mutation and one non-carrier family member. . 2024-10-00. DOI: 10.1016/j.scr.2024.103497 UMCUi001-AUMCUi002-AUMCUi003-AUMCUi004-A 2024-10-00 2024-10-00 DOI: 10.1016/j.scr.2024.103497Associated cell lines:
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Shin Yoo Jin, Chae Seung Yun, Lee Hanbi, Fang Xianying, Cui Sheng, Lim Sun Woo, Lee Kang In, Lee Jae Young, Li Can, Yang Chul Woo, Chung Byung Ha
CRISPR/Cas9-mediated suppression of A4GALT rescues endothelial cell dysfunction in a fabry disease vasculopathy model derived from human induced pluripotent stem cells
Shin Yoo Jin et al. CRISPR/Cas9-mediated suppression of A4GALT rescues endothelial cell dysfunction in a fabry disease vasculopathy model derived from human induced pluripotent stem cells. . 2024-10-00. DOI: 10.1016/j.atherosclerosis.2024.118549 CMCi006-ACMCi007-A 2024-10-00 2024-10-00 DOI: 10.1016/j.atherosclerosis.2024.118549 -
Wang X, Zhuang H, Tan Y, Lei F, Li C, Zhang C, Yu X, Sang H
Generation of a human induced pluripotent stem cell (iPSC, DVSi001-A) with a heterozygous mutation in KRAS (A209T)
Wang X et al. Generation of a human induced pluripotent stem cell (iPSC, DVSi001-A) with a heterozygous mutation in KRAS (A209T). . 2024-10-00. Pubmed ID: 39106598; DOI: 10.1016/j.scr.2024.103528 DVSi001-A 2024-10-00 2024-10-00 PubMed: 39106598 DOI: 10.1016/j.scr.2024.103528Associated cell lines:
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Bai Ruiqi, Hao Lixia, Zhou Guiwen, Fu Qiang, Zhang Peixuan, Lin Pianpian, Chen Minliang
The mechanism of TGF-β mediating BRD4/STAT3 signaling pathway to promote fibroblast proliferation and thus promote keloid progression
Bai Ruiqi et al. The mechanism of TGF-β mediating BRD4/STAT3 signaling pathway to promote fibroblast proliferation and thus promote keloid progression. . 2024-10-00. DOI: 10.1016/j.heliyon.2024.e38188 HEBHMUi015-A 2024-10-00 2024-10-00 DOI: 10.1016/j.heliyon.2024.e38188Associated cell lines:
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Tang P, Keshi E, Wilken S, Wutsdorff L, Mougnekabol J, Pratschke J, Sauer IM, Haep N
Generation of an induced pluripotent stem cell (iPSC) line (EXSURGi001-A) from a patient homozygous for the p.Ala165Thr mutation in the MTARC1 gene
Tang P et al. Generation of an induced pluripotent stem cell (iPSC) line (EXSURGi001-A) from a patient homozygous for the p.Ala165Thr mutation in the MTARC1 gene. . 2024-10-00. Pubmed ID: 39094505; DOI: 10.1016/j.scr.2024.103516 EXSURGi001-A 2024-10-00 2024-10-00 PubMed: 39094505 DOI: 10.1016/j.scr.2024.103516Associated cell lines:
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Wang B, Yang L, Gao M, Zhang H, Ji A, Liu G, Liu Y
Establishment of a human induced pluripotent stem cell line (SDQLCHi079-A) from a patient with Johanson-Blizzard syndrome carrying heterozygous mutation in UBR1 gene
Wang B et al. Establishment of a human induced pluripotent stem cell line (SDQLCHi079-A) from a patient with Johanson-Blizzard syndrome carrying heterozygous mutation in UBR1 gene. . 2024-10-00. Pubmed ID: 39053320; DOI: 10.1016/j.scr.2024.103505 SDQLCHi079-A 2024-10-00 2024-10-00 PubMed: 39053320 DOI: 10.1016/j.scr.2024.103505Associated cell lines:
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Pornratananont G, Tangprasittipap A, Hongeng S, Anurathapan U
Generation of integration-free human induced pluripotent stem cell line MURAi003-A derived from the peripheral blood mononuclear cells of a donor with homozygous Class I and Class II HLAs (A*11:01, B*46:01; C*01:02; DRB1*09:01; DQB1*03:03)
Pornratananont G et al. Generation of integration-free human induced pluripotent stem cell line MURAi003-A derived from the peripheral blood mononuclear cells of a donor with homozygous Class I and Class II HLAs (A*11:01, B*46:01; C*01:02; DRB1*09:01; DQB1*03:03). . 2024-10-00. Pubmed ID: 39083857; DOI: 10.1016/j.scr.2024.103514 MUi010-AMUi015-AMUi031-AMURAi003-A 2024-10-00 2024-10-00 PubMed: 39083857 DOI: 10.1016/j.scr.2024.103514Associated cell lines:
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Fatima N, Dillen L, Hommersom MP, Çepni E, Fatima F, van Beusekom E, Albert S, Ali Khan A, de Brouwer APM, van Bokhoven H
Generation of induced pluripotent stem cell line (UCSFi001-A-77) carrying a biallelic frameshift variant in exon 4 of SGIP1 through CRISPR/Cas9
Fatima N et al. Generation of induced pluripotent stem cell line (UCSFi001-A-77) carrying a biallelic frameshift variant in exon 4 of SGIP1 through CRISPR/Cas9. . 2024-10-00. Pubmed ID: 39098170; DOI: 10.1016/j.scr.2024.103511 UCSFi001-AUCSFi001-A-77 2024-10-00 2024-10-00 PubMed: 39098170 DOI: 10.1016/j.scr.2024.103511Associated cell lines:
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Heider Johanna, González Emilio Pardo, Hartmann Sophia-Marie, Kannaiyan Nirmal, Vogel Sabrina, Wüst Richard, Fallgatter Andreas J., Rossner Moritz J., Kraushaar Udo, Volkmer Hansjürgen
Aberrant neuronal connectivity and network activity of neurons derived from patients with idiopathic schizophrenia
Heider Johanna et al. Aberrant neuronal connectivity and network activity of neurons derived from patients with idiopathic schizophrenia. . 2024-10-00. DOI: 10.1016/j.nbd.2024.106678 NMIi010-A 2024-10-00 2024-10-00 DOI: 10.1016/j.nbd.2024.106678Associated cell lines:
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Vacante F, Venkateshappa R, Htet M, Yan C, Wu JC
Generation of Marfan syndrome-specific induced pluripotent stem cells harboring FBN1 mutations
Vacante F et al. Generation of Marfan syndrome-specific induced pluripotent stem cells harboring FBN1 mutations. . 2024-10-00. Pubmed ID: 39096853; DOI: 10.1016/j.scr.2024.103518 SCVIi128-ASCVIi129-A 2024-10-00 2024-10-00 PubMed: 39096853 DOI: 10.1016/j.scr.2024.103518Associated cell lines:
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Qin H, Yu Y, Ye S, Alonzo M, Garg V, Zhao MT
Generation of an induced pluripotent stem cell line (NCHi016-A) from a 5-year-old female with pulmonary atresia with intact ventricular septum and one-and-half ventricle palliation
Qin H et al. Generation of an induced pluripotent stem cell line (NCHi016-A) from a 5-year-old female with pulmonary atresia with intact ventricular septum and one-and-half ventricle palliation. . 2024-10-00. Pubmed ID: 39126918; DOI: 10.1016/j.scr.2024.103530; PMC: PMC11411636 NCHi016-A 2024-10-00 2024-10-00 PubMed: 39126918 DOI: 10.1016/j.scr.2024.103530Associated cell lines:
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Jin Meng, Zhang Guowei, Wang Shouqi, Zhao Rou, Zhang Haitao
ISL1 and AQP5 complement each other to enhance gastric cancer cell stemness by regulating CD44 expression
Jin Meng et al. ISL1 and AQP5 complement each other to enhance gastric cancer cell stemness by regulating CD44 expression. . 2024-10-00. DOI: 10.21037/tcr-24-248 WAe009-AWAe009-A-1G 2024-10-00 2024-10-00 DOI: 10.21037/tcr-24-248Associated cell lines:
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Wang L, Guo R, Zhang X, Zhou Z, Yao Akogo H, Fu Z, Song Y, Li M, Ma J
An integration-free induced pluripotent stem cell line from a 42-year-old female donor with the APOE-ε2/ε2 allele
Wang L et al. An integration-free induced pluripotent stem cell line from a 42-year-old female donor with the APOE-ε2/ε2 allele. . 2024-10-00. Pubmed ID: 39094506; DOI: 10.1016/j.scr.2024.103506 HEBHMUi017-A 2024-10-00 2024-10-00 PubMed: 39094506 DOI: 10.1016/j.scr.2024.103506Associated cell lines:
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Zhang Denglu, Li KaiLin, Yang XianZhen, Wang Haitao, Yu Xin
Establishment of an induced pluripotent stem cell line from a patient with X-linked Alport syndrome carrying a hemizygous splicing variant (NM_033380; c.929[exon 16]delG) in the collagen type IV alpha 5 chain gene
Zhang Denglu et al. Establishment of an induced pluripotent stem cell line from a patient with X-linked Alport syndrome carrying a hemizygous splicing variant (NM_033380; c.929[exon 16]delG) in the collagen type IV alpha 5 chain gene. . 2024-10-00. DOI: 10.1016/j.scr.2024.103488 SHTCMi001-A 2024-10-00 2024-10-00 DOI: 10.1016/j.scr.2024.103488Associated cell lines:
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Jiang S, Dai T, Li Q, Xu T, Zhang W, Sun J, Liu H
Generation of ASCL1-mCherry knock-in reporter in human embryonic stem cell line, WAe001-A-2E, using CRISPR/Cas9-based gene targeting
Jiang S et al. Generation of ASCL1-mCherry knock-in reporter in human embryonic stem cell line, WAe001-A-2E, using CRISPR/Cas9-based gene targeting. . 2024-10-00. Pubmed ID: 39059080; DOI: 10.1016/j.scr.2024.103500 WAe001-AWAe001-A-2E 2024-10-00 2024-10-00 PubMed: 39059080 DOI: 10.1016/j.scr.2024.103500Associated cell lines:
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Dexheimer R, Manhas A, Wu D, Tripathi D, Yu Chan S, Li J, Yu R, Sayed N, Wu JC, Sallam K
Generation of two iPSC lines from dilated cardiomyopathy patients with pathogenic variants in the SCN5A gene
Dexheimer R et al. Generation of two iPSC lines from dilated cardiomyopathy patients with pathogenic variants in the SCN5A gene. . 2024-10-00. Pubmed ID: 39067410; DOI: 10.1016/j.scr.2024.103498 SCVIi121-ASCVIi123-A 2024-10-00 2024-10-00 PubMed: 39067410 DOI: 10.1016/j.scr.2024.103498Associated cell lines:
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Ma Shi-chao, Xie Yi-lin, Wang Qian, Fu Shan-gui, Wu Hong-ze
Application of eye organoids in the study of eye diseases
Ma Shi-chao et al. Application of eye organoids in the study of eye diseases. . 2024-10-00. DOI: 10.1016/j.exer.2024.110068 CUIMCi005-A 2024-10-00 2024-10-00 DOI: 10.1016/j.exer.2024.110068Associated cell lines:
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Clayton Joshua S., Vo Christina, Crane Jordan, Scriba Carolin K., Saker Safaa, Larmonier Thierry, Malfatti Edoardo, Romero Norma B., Ravenscroft Gianina, Laing Nigel G., Taylor Rhonda L.
Generation of iPSC lines from three Laing distal myopathy patients with a recurrent MYH7 p.Lys1617del variant
Clayton Joshua S. et al. Generation of iPSC lines from three Laing distal myopathy patients with a recurrent MYH7 p.Lys1617del variant. . 2024-10-00. DOI: 10.1016/j.scr.2024.103491 SCTi003-A 2024-10-00 2024-10-00 DOI: 10.1016/j.scr.2024.103491Associated cell lines:
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Claeys Kristl G., Savarese Marco, Jonson Per Harald, Goosens Veerle, Topf Ana, Vihola Anna, Straub Volker, Udd Bjarne
A Titin Truncating Variant Causing a Dominant Myopathy With Cardiac Involvement in a Large Family
Claeys Kristl G. et al. A Titin Truncating Variant Causing a Dominant Myopathy With Cardiac Involvement in a Large Family. . 2024-10-00. DOI: 10.1212/nxg.0000000000200185 YCMi004-A 2024-10-00 2024-10-00 DOI: 10.1212/nxg.0000000000200185Associated cell lines:
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Zhang H, Zhang Q, Chen X, Wang M, Li L, Yu C
Establishment of a transgene-free iPS cell line (SDCHi008-A) from a young patient bearing a KCNQ2 mutation and suffering from Epilepsy
Zhang H et al. Establishment of a transgene-free iPS cell line (SDCHi008-A) from a young patient bearing a KCNQ2 mutation and suffering from Epilepsy. . 2024-10-00. Pubmed ID: 39079397; DOI: 10.1016/j.scr.2024.103507 SDCHi008-A 2024-10-00 2024-10-00 PubMed: 39079397 DOI: 10.1016/j.scr.2024.103507Associated cell lines:
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Muhammad Z, Brown PW, Babazau L, Alkhamis AI, Goni BW, Nggada HA, Mbaya KM, Wray S, Marte IH, Karch CM, Serpell LC, Maina MB
Generation of an induced pluripotent stem cell line (BIORTCi001-A) from a healthy adult indigenous Nigerian participant
Muhammad Z et al. Generation of an induced pluripotent stem cell line (BIORTCi001-A) from a healthy adult indigenous Nigerian participant. . 2024-10-00. Pubmed ID: 39067409; DOI: 10.1016/j.scr.2024.103503 BIORTCi001-A 2024-10-00 2024-10-00 PubMed: 39067409 DOI: 10.1016/j.scr.2024.103503Associated cell lines:
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Lin Chensheng, Liu Shiyu, Huang Minjun, Zhang Yanding, Hu Xuefeng
Induction of human stem cells into ameloblasts by reaggregation strategy
Lin Chensheng et al. Induction of human stem cells into ameloblasts by reaggregation strategy. . 2024-09-27. DOI: 10.1186/s13287-024-03948-1 UNIPDi001-A 2024-09-27 2024-09-27 DOI: 10.1186/s13287-024-03948-1Associated cell lines:
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Ahmed H. Shafeeq
The Multifaceted Role of L-Type Amino Acid Transporter 1 at the Blood–Brain Barrier: Structural Implications and Therapeutic Potential
Ahmed H. Shafeeq. The Multifaceted Role of L-Type Amino Acid Transporter 1 at the Blood–Brain Barrier: Structural Implications and Therapeutic Potential. . 2024-09-26. DOI: 10.1007/s12035-024-04506-9 BIONi010-C 2024-09-26 2024-09-26 DOI: 10.1007/s12035-024-04506-9Associated cell lines:
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E S K, A K Z, M Yu S, K I P, N L R, E G N, K S S, A A K, T L V, A S M, E N M, T M P, E S V, A A K
Distinct molecular features of FLNC mutations, associated with different clinical phenotypes
E S K et al. Distinct molecular features of FLNC mutations, associated with different clinical phenotypes. . 2024-09-24. Pubmed ID: 39315490; DOI: 10.1002/cm.21922 FAMRCi009-AFAMRCi011-A 2024-09-24 2024-09-24 PubMed: 39315490 DOI: 10.1002/cm.21922Associated cell lines:
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Sheveleva O. N., Nenasheva T. A., Lyadova I. V.
Early markers of induced pluripotent stem cell hematopoietic development
Sheveleva O. N. et al. Early markers of induced pluripotent stem cell hematopoietic development. . 2024-09-21. DOI: 10.15789/1563-0625-emo-16759 ICGi021-AICGi022-A 2024-09-21 2024-09-21 DOI: 10.15789/1563-0625-emo-16759 -
Remmert C, Otgonbayar M, Perschel JA, Marder M, Meier M
Protocol to generate a microfluidic vessels-on-chip platform using human pluripotent stem cell-derived endothelial cells
Remmert C et al. Protocol to generate a microfluidic vessels-on-chip platform using human pluripotent stem cell-derived endothelial cells. . 2024-09-20. Pubmed ID: 39244759; DOI: 10.1016/j.xpro.2024.103300; PMC: PMC11407103 HMGUi001-A 2024-09-20 2024-09-20 PubMed: 39244759 DOI: 10.1016/j.xpro.2024.103300Associated cell lines:
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Petersilie L, Kafitz KW, Neu LA, Heiduschka S, Le S, Prigione A, Rose CR
Protocol for the generation of cultured cortical brain organoid slices
Petersilie L et al. Protocol for the generation of cultured cortical brain organoid slices. . 2024-09-20. Pubmed ID: 39128007; DOI: 10.1016/j.xpro.2024.103212; PMC: PMC11369419 HVRDi004-BHMGUi001-AHHUUKDi009-A 2024-09-20 2024-09-20 PubMed: 39128007 DOI: 10.1016/j.xpro.2024.103212Associated cell lines:
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Bozhokin Mikhail S., Marchenko Daria M., Mikhaylova Elena R., Rakhimov Bulat R., Bozhkova Svetlana A., Korneva Yulia S., Aleksandrova Svetlana A., Khotin Mikhail G.
Evaluation of chondrogenic potential of human dermal fibroblasts after modification with differentiation media and cytokine TGF-β3
Bozhokin Mikhail S. et al. Evaluation of chondrogenic potential of human dermal fibroblasts after modification with differentiation media and cytokine TGF-β3. . 2024-09-20. DOI: 10.17816/gc632926 HEBHMUi015-A 2024-09-20 2024-09-20 DOI: 10.17816/gc632926Associated cell lines:
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Fasano C, Cavaliere A, Tiranti V, Peron C
Protocol for evaluating mitochondrial respiration in iPSC-derived neurons by the Seahorse XF analyzer
Fasano C et al. Protocol for evaluating mitochondrial respiration in iPSC-derived neurons by the Seahorse XF analyzer. . 2024-09-20. Pubmed ID: 39012842; DOI: 10.1016/j.xpro.2024.103127; PMC: PMC11283151 FINCBi001-AFINCBi002-AFINCBi003-A 2024-09-20 2024-09-20 PubMed: 39012842 DOI: 10.1016/j.xpro.2024.103127Associated cell lines:
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Yan Hao, Zang Ruge, Cui Tiantian, Liu Yiming, Zhang Biao, Zhao Lingpin, Li Hongyu, Zhou Juannian, Wang Haiyang, Zeng Quan, Xu Lei, Zhou Yuqi, Pei Xuetao, Xi Jiafei, Yue Wen
PROTAC-mediated vimentin degradation promotes terminal erythroid differentiation of pluripotent stem cells
Yan Hao et al. PROTAC-mediated vimentin degradation promotes terminal erythroid differentiation of pluripotent stem cells. . 2024-09-18. DOI: 10.1186/s13287-024-03910-1 IHSTMi001-A 2024-09-18 2024-09-18 DOI: 10.1186/s13287-024-03910-1Associated cell lines:
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Giacomoni J, Bruzelius A, Habekost M, Kajtez J, Ottosson DR, Fiorenzano A, Storm P, Parmar M
3D model for human glia conversion into subtype-specific neurons, including dopamine neurons
Giacomoni J et al. 3D model for human glia conversion into subtype-specific neurons, including dopamine neurons. . 2024-09-16. Pubmed ID: 39236715; DOI: 10.1016/j.crmeth.2024.100845; PMC: PMC11440053 RCe021-A 2024-09-16 2024-09-16 PubMed: 39236715 DOI: 10.1016/j.crmeth.2024.100845Associated cell lines:
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Graceffo E, Opitz R, Megges M, Krude H, Schuelke M
RNA Sequencing Reveals a Strong Predominance of THRA Splicing Isoform 2 in the Developing and Adult Human Brain
Graceffo E et al. RNA Sequencing Reveals a Strong Predominance of THRA Splicing Isoform 2 in the Developing and Adult Human Brain. . 2024-09-13. Pubmed ID: 39337374; DOI: 10.3390/ijms25189883; PMC: PMC11432079 BIHi005-ABIHi001-BHMGUi001-A 2024-09-13 2024-09-13 PubMed: 39337374 DOI: 10.3390/ijms25189883Associated cell lines:
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Retter Ida, Behm Laura, Grohmann Lisa, Schmelz Karin, Rosowski Jennifer, Hippenstiel Stefan
3R centres contributions to change animal experimentation
Retter Ida et al. 3R centres contributions to change animal experimentation. . 2024-09-13. DOI: 10.1038/s44319-024-00262-y BCRTi006-ABCRTi007-A 2024-09-13 2024-09-13 DOI: 10.1038/s44319-024-00262-yAssociated cell lines:
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Rezaeiani S, Rezaee M, Shafaghi M, Karami M, Hamidi R, Khodayari H, Vahdat S, Pahlavan S, Baharvand H
Expandable hESC-derived cardiovascular progenitor cells generate functional cardiac lineage cells for microtissue construction
Rezaeiani S et al. Expandable hESC-derived cardiovascular progenitor cells generate functional cardiac lineage cells for microtissue construction. . 2024-09-12. Pubmed ID: 39267174; DOI: 10.1186/s13287-024-03919-6; PMC: PMC11396807 RIe006-A 2024-09-12 2024-09-12 PubMed: 39267174 DOI: 10.1186/s13287-024-03919-6Associated cell lines:
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Qi L, Groeger M, Sharma A, Goswami I, Chen E, Zhong F, Ram A, Healy K, Hsiao EC, Willenbring H, Stahl A
Adipocyte inflammation is the primary driver of hepatic insulin resistance in a human iPSC-based microphysiological system
Qi L et al. Adipocyte inflammation is the primary driver of hepatic insulin resistance in a human iPSC-based microphysiological system. . 2024-09-12. Pubmed ID: 39266553; DOI: 10.1038/s41467-024-52258-w; PMC: PMC11393072 UCSFi001-A 2024-09-12 2024-09-12 PubMed: 39266553 DOI: 10.1038/s41467-024-52258-wAssociated cell lines:
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Joshi Jyotsna, Albers Cora, Smole Nathan, Guo Shuliang, Smith Sakima A.
Human induced pluripotent stem cell-derived cardiomyocytes (iPSC-CMs) for modeling cardiac arrhythmias: strengths, challenges and potential solutions
Joshi Jyotsna et al. Human induced pluripotent stem cell-derived cardiomyocytes (iPSC-CMs) for modeling cardiac arrhythmias: strengths, challenges and potential solutions. . 2024-09-12. DOI: 10.3389/fphys.2024.1475152 INSRMi008-AINSRMi009-AINSRMi010-A 2024-09-12 2024-09-12 DOI: 10.3389/fphys.2024.1475152Associated cell lines:
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Micolonghi Caterina, Perrone Federica, Fabiani Marco, Caroselli Silvia, Savio Camilla, Pizzuti Antonio, Germani Aldo, Visco Vincenzo, Petrucci Simona, Rubattu Speranza, Piane Maria
Unveiling the Spectrum of Minor Genes in Cardiomyopathies: A Narrative Review
Micolonghi Caterina et al. Unveiling the Spectrum of Minor Genes in Cardiomyopathies: A Narrative Review. . 2024-09-10. DOI: 10.3390/ijms25189787 ZZUNEUi026-A 2024-09-10 2024-09-10 DOI: 10.3390/ijms25189787Associated cell lines:
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Sun Wenxian, Chen Yufei, Yang Yuting, Wang Pin, Gong Jin, Han Xiaodong, Xu Chang, Luan Heya, Li Shaoqi, Li Ruina, Wen Boye, Lv Sirong, Wei Cuibai
Characteristics and Transcriptomic Analysis of Cholinergic Neurons Derived from Induced Pluripotent Stem Cells with APP Mutation in Alzheimer’s Disease
Sun Wenxian et al. Characteristics and Transcriptomic Analysis of Cholinergic Neurons Derived from Induced Pluripotent Stem Cells with APP Mutation in Alzheimer’s Disease. . 2024-09-10. DOI: 10.3233/jad-240299 XWHNi001-A 2024-09-10 2024-09-10 DOI: 10.3233/jad-240299Associated cell lines:
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Clark Branden J, Lelos Mariah J, Loring Jeanne F
Advancing Parkinson’s disease treatment: cell replacement therapy with neurons derived from pluripotent stem cells
Clark Branden J et al. Advancing Parkinson’s disease treatment: cell replacement therapy with neurons derived from pluripotent stem cells. . 2024-09-10. DOI: 10.1093/stmcls/sxae042 RCe021-A 2024-09-10 2024-09-10 DOI: 10.1093/stmcls/sxae042Associated cell lines:
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Yi R, Chen S, Guan M, Liao C, Zhu Y, Ip JPK, Ye T, Chen Y
A single-cell transcriptomic dataset of pluripotent stem cell-derived astrocytes via NFIB/SOX9 overexpression
Yi R et al. A single-cell transcriptomic dataset of pluripotent stem cell-derived astrocytes via NFIB/SOX9 overexpression. . 2024-09-10. Pubmed ID: 39256463; DOI: 10.1038/s41597-024-03823-x; PMC: PMC11387634 BIONi037-A 2024-09-10 2024-09-10 PubMed: 39256463 DOI: 10.1038/s41597-024-03823-xAssociated cell lines:
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Niu Wenkang, Li Guifang, Zhang Tingting, Ma Lei
Prostate cancer subtyping and differential methylation analysis based on the ETS family of transcription factors fusion genes
Niu Wenkang et al. Prostate cancer subtyping and differential methylation analysis based on the ETS family of transcription factors fusion genes. . 2024-09-06. DOI: 10.1038/s41598-024-71285-7 WAe001-A-44 2024-09-06 2024-09-06 DOI: 10.1038/s41598-024-71285-7Associated cell lines:
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Thamarai P, Karishma S, Kamalesh R, Shaji A, Saravanan A, Bibi S, Vickram AS, Chopra H, Saleem RA, Alsharif KF, Theyab A, Kamel M, Alamoudi MK, Kumer A, Chopra S, Abdel-Daim MM
Current advancements in nanotechnology for stem cells
Thamarai P et al. Current advancements in nanotechnology for stem cells. . 2024-09-05. Pubmed ID: 39236089; DOI: 10.1097/js9.0000000000002082; PMC: PMC11634102 SKLRMe001-A 2024-09-05 2024-09-05 PubMed: 39236089 DOI: 10.1097/js9.0000000000002082Associated cell lines:
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Gerasimova Tatiana, Poberezhniy Daniil, Nenasheva Valentina, Stepanenko Ekaterina, Arsenyeva Elena, Novosadova Lyudmila, Grivennikov Igor, Illarioshkin Sergey, Lagarkova Maria, Tarantul Vyacheslav, Novosadova Ekaterina
Inflammatory Intracellular Signaling in Neurons Is Influenced by Glial Soluble Factors in iPSC-Based Cell Model of PARK2-Associated Parkinson’s Disease
Gerasimova Tatiana et al. Inflammatory Intracellular Signaling in Neurons Is Influenced by Glial Soluble Factors in iPSC-Based Cell Model of PARK2-Associated Parkinson’s Disease. . 2024-09-05. DOI: 10.3390/ijms25179621 RCPCMi004-A 2024-09-05 2024-09-05 DOI: 10.3390/ijms25179621Associated cell lines:
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Hutschalik T, Özgül O, Casini M, Szabó B, Peyronnet R, Bártulos Ó, Argenziano M, Schotten U, Matsa E
Immune response caused by M1 macrophages elicits atrial fibrillation-like phenotypes in coculture model with isogenic hiPSC-derived cardiomyocytes
Hutschalik T et al. Immune response caused by M1 macrophages elicits atrial fibrillation-like phenotypes in coculture model with isogenic hiPSC-derived cardiomyocytes. . 2024-09-04. Pubmed ID: 39227896; DOI: 10.1186/s13287-024-03814-0; PMC: PMC11373469 CRMi001-A 2024-09-04 2024-09-04 PubMed: 39227896 DOI: 10.1186/s13287-024-03814-0Associated cell lines:
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Díaz Alicia González, Possenti Andrea, Urrutia Gustavo Antonio, Bian Yuqi, Kedia Shekhar, Boeken Dorothea, Lim Christine M., Licastro Danilo, Mannini Benedetta, Klenerman David, Vendruscolo Michele
A human neuronal model of sporadic Alzheimer’s disease induced byFBXO2downregulation shows Aβ aggregation, tau hyperphosphorylation and functional network impairment
Díaz Alicia González et al. A human neuronal model of sporadic Alzheimer’s disease induced byFBXO2downregulation shows Aβ aggregation, tau hyperphosphorylation and functional network impairment. . 2024-09-03. DOI: 10.1101/2024.09.01.610673 BIONi010-CBIONi010-C-38 2024-09-03 2024-09-03 DOI: 10.1101/2024.09.01.610673Associated cell lines:
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Stepanov AI, Shuvaeva AA, Putlyaeva LV, Lukyanov DK, Galiakberova AA, Gorbachev DA, Maltsev DI, Pronina V, Dylov DV, Terskikh AV, Lukyanov KA, Gurskaya NG
Tracking induced pluripotent stem cell differentiation with a fluorescent genetically encoded epigenetic probe
Stepanov AI et al. Tracking induced pluripotent stem cell differentiation with a fluorescent genetically encoded epigenetic probe. . 2024-09-02. Pubmed ID: 39222083; DOI: 10.1007/s00018-024-05359-0; PMC: PMC11368889 KUIFMSi004-AKUIFMSi004-A-1 2024-09-02 2024-09-02 PubMed: 39222083 DOI: 10.1007/s00018-024-05359-0Associated cell lines:
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Law Christine, Pattathil Niveditha, Simpson Hailey, Ward Michael J., Lampen Shaun, Kamath Binita, Aleman Tomas S.
Intraretinal hemorrhages and detailed retinal phenotype of three patients with Alagille syndrome
Law Christine et al. Intraretinal hemorrhages and detailed retinal phenotype of three patients with Alagille syndrome. . 2024-09-02. DOI: 10.1080/13816810.2024.2362214 TRNDi031-A 2024-09-02 2024-09-02 DOI: 10.1080/13816810.2024.2362214Associated cell lines:
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Baggiani M, Santorelli FM, Mero S, Privitera F, Damiani D, Tessa A
Generation of a human induced pluripotent stem cell line (FSMi001-A) from fibroblasts of a patient carrying heterozygous mutation in the REEP1 gene
Baggiani M et al. Generation of a human induced pluripotent stem cell line (FSMi001-A) from fibroblasts of a patient carrying heterozygous mutation in the REEP1 gene. . 2024-09-00. Pubmed ID: 38889632; DOI: 10.1016/j.scr.2024.103472; PMC: PMC11307172 FSMi001-A 2024-09-00 2024-09-00 PubMed: 38889632 DOI: 10.1016/j.scr.2024.103472Associated cell lines:
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Ning J, Zhou T, Luo X, Ma J, Zhang Z, Gao L, Zhu Y
Establishment of an iPSC line from a NDD patient with a heterozygous mutation in the CTNNB1 gene
Ning J et al. Establishment of an iPSC line from a NDD patient with a heterozygous mutation in the CTNNB1 gene. . 2024-09-00. Pubmed ID: 38972232; DOI: 10.1016/j.scr.2024.103487 CTUi005-A 2024-09-00 2024-09-00 PubMed: 38972232 DOI: 10.1016/j.scr.2024.103487Associated cell lines:
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Qin Y, Godoy-Parejo C, Skowronska M, Verma A, Dejosez M, Zwaka TP
Generation of human pluripotent stem cell lines (WAe009-A) with THAP11(F80L) cobalamin disorder-associated mutation
Qin Y et al. Generation of human pluripotent stem cell lines (WAe009-A) with THAP11(F80L) cobalamin disorder-associated mutation. . 2024-09-00. Pubmed ID: 38943762; DOI: 10.1016/j.scr.2024.103483 WAe009-A 2024-09-00 2024-09-00 PubMed: 38943762 DOI: 10.1016/j.scr.2024.103483Associated cell lines:
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Alowaysi M, Baadhaim M, Al-Shehri M, Alzahrani H, Badkok A, Attas H, Zakri S, Alameer S, Malibari D, Hosawi M, Daghestani M, Al-Ghamdi K, Muharraq M, Zia A, Tegne J, Alfadhel M, Aboalola D, Alsayegh K
Derivation of two iPSC lines (KAIMRCi004-A, KAIMRCi004-B) from a Saudi patient with Biotin-Thiamine-responsive Basal Ganglia Disease (BTBGD) carrying homozygous pathogenic missense variant in the SCL19A3 gene
Alowaysi M et al. Derivation of two iPSC lines (KAIMRCi004-A, KAIMRCi004-B) from a Saudi patient with Biotin-Thiamine-responsive Basal Ganglia Disease (BTBGD) carrying homozygous pathogenic missense variant in the SCL19A3 gene. . 2024-09-00. Pubmed ID: 38980565; DOI: 10.1007/s13577-024-01097-4; PMC: PMC11341592 KAIMRCi004-AKAIMRCi004-B 2024-09-00 2024-09-00 PubMed: 38980565 DOI: 10.1007/s13577-024-01097-4Associated cell lines:
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Pierre Marion, Djemai Mohammed, Pouliot Valérie, Poulin Hugo, Gollob Michael H., Chahine Mohamed
Exploring SCN5A variants associated with atrial fibrillation in atrial cardiomyocytes derived from human induced pluripotent stem cells: A characterization study
Pierre Marion et al. Exploring SCN5A variants associated with atrial fibrillation in atrial cardiomyocytes derived from human induced pluripotent stem cells: A characterization study. . 2024-09-00. DOI: 10.1016/j.hrthm.2024.09.013 CBRCULi008-ACBRCULi009-A 2024-09-00 2024-09-00 DOI: 10.1016/j.hrthm.2024.09.013Associated cell lines:
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Takagi D, Tsukamoto S, Nakade K, Shimizu T, Arai Y, Matsuo-Takasaki M, Noguchi M, Nakamura Y, Yumoto N, Kawada J, Hayata T, Hayashi Y
Generation of MBP-tdTomato reporter human induced pluripotent stem cell line for live myelin visualization
Takagi D et al. Generation of MBP-tdTomato reporter human induced pluripotent stem cell line for live myelin visualization. . 2024-09-00. Pubmed ID: 39032428; DOI: 10.1016/j.scr.2024.103493 BRCi014-A-3 2024-09-00 2024-09-00 PubMed: 39032428 DOI: 10.1016/j.scr.2024.103493Associated cell lines:
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Arai D, Takahashi-Shibata M, Ukaji T, Tsutsumi H, Tajima S, Nishio SY, Ishikawa KI, Akamatsu W, Matsumoto F, Ikeda K, Usami SI, Kamiya K
Generation of an induced pluripotent stem cell line from a late-onset, progressive high frequency hearing loss patient due to mutation in CDH23
Arai D et al. Generation of an induced pluripotent stem cell line from a late-onset, progressive high frequency hearing loss patient due to mutation in CDH23. . 2024-09-00. Pubmed ID: 38878669; DOI: 10.1016/j.scr.2024.103471 JUFMDOi008-A 2024-09-00 2024-09-00 PubMed: 38878669 DOI: 10.1016/j.scr.2024.103471Associated cell lines:
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Ltaief SM, Elsayed AK, Al-Shammari AR
Generation of nine induced pluripotent stem cell lines from six young children with autism spectrum disorder and three matched control subjects from the Qatari population
Ltaief SM et al. Generation of nine induced pluripotent stem cell lines from six young children with autism spectrum disorder and three matched control subjects from the Qatari population. . 2024-09-00. Pubmed ID: 38896970; DOI: 10.1016/j.scr.2024.103470 QBRIi019-AQBRIi020-AQBRIi021-AQBRIi022-AQBRIi023-AQBRIi024-BQBRIi025-AQBRIi026-AQBRIi027-B 2024-09-00 2024-09-00 PubMed: 38896970 DOI: 10.1016/j.scr.2024.103470Associated cell lines:
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Wang X, Gao J, Liu C, Sun J
Establishment of human embryonic stem cell lines carrying LQT1 mutations by CRISPR base editing
Wang X et al. Establishment of human embryonic stem cell lines carrying LQT1 mutations by CRISPR base editing. . 2024-09-00. Pubmed ID: 39018827; DOI: 10.1016/j.scr.2024.103496 WAe009-AWAe009-A-1L 2024-09-00 2024-09-00 PubMed: 39018827 DOI: 10.1016/j.scr.2024.103496Associated cell lines:
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Hall FD 3rd, Miller CN, Gerecht S, Boheler KR
Generation of an induced pluripotent stem cell line, JHUi005-A, from a Marfan Syndrome patient harboring a pathogenic c.3338-2A>C intronic splicing variant
Hall FD 3rd et al. Generation of an induced pluripotent stem cell line, JHUi005-A, from a Marfan Syndrome patient harboring a pathogenic c.3338-2A>C intronic splicing variant. . 2024-09-00. Pubmed ID: 38941881; DOI: 10.1016/j.scr.2024.103475 JHUi005-A 2024-09-00 2024-09-00 PubMed: 38941881 DOI: 10.1016/j.scr.2024.103475Associated cell lines:
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Volke L, Daya NM, Döring K, Rohm M, Athamneh M, Zaehres H, Roos A, Güttsches AK, Mavrommatis L, Vorgerd M
Generation of two induced pluripotent stem cell lines (HIMRi006-A and HIMRi007-A) from Pompe patients with infantile and late disease onset
Volke L et al. Generation of two induced pluripotent stem cell lines (HIMRi006-A and HIMRi007-A) from Pompe patients with infantile and late disease onset. . 2024-09-00. Pubmed ID: 38896971; DOI: 10.1016/j.scr.2024.103459 HIMRi001-AHIMRi006-AHIMRi007-A 2024-09-00 2024-09-00 PubMed: 38896971 DOI: 10.1016/j.scr.2024.103459Associated cell lines:
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Zanetti Alessandra, Tomanin Rosella
Targeting Neurological Aspects of Mucopolysaccharidosis Type II: Enzyme Replacement Therapy and Beyond
Zanetti Alessandra et al. Targeting Neurological Aspects of Mucopolysaccharidosis Type II: Enzyme Replacement Therapy and Beyond. . 2024-09-00. DOI: 10.1007/s40259-024-00675-0 CSSi014-A 2024-09-00 2024-09-00 DOI: 10.1007/s40259-024-00675-0Associated cell lines:
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Tangprasittipap A, Innachai P, Chumchuen S, Chiangjong W, Jinawath N, Sirachainan N, Hongeng S
Establishment of human induced pluripotent stem cell line MURAi001-A from skin fibroblasts of a patient carrying a c.4404A > G mutation in the TET1 gene
Tangprasittipap A et al. Establishment of human induced pluripotent stem cell line MURAi001-A from skin fibroblasts of a patient carrying a c.4404A > G mutation in the TET1 gene. . 2024-09-00. Pubmed ID: 38909482; DOI: 10.1016/j.scr.2024.103474 MUi015-AMURAi001-A 2024-09-00 2024-09-00 PubMed: 38909482 DOI: 10.1016/j.scr.2024.103474Associated cell lines:
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Wong EYM, Khoh XE, Chen SC, Lye J, Leith FK, Zhang D, Lamey TM, Thompson JA, McLaren TL, Atlas MD, Chen FK, McLenachan S
Generation of two induced pluripotent stem cell lines from an Usher syndrome type 1B patient with the homozygous c.496del MYO7A variant
Wong EYM et al. Generation of two induced pluripotent stem cell lines from an Usher syndrome type 1B patient with the homozygous c.496del MYO7A variant. . 2024-09-00. Pubmed ID: 39013239; DOI: 10.1016/j.scr.2024.103492 LEIi020-ALEIi020-B 2024-09-00 2024-09-00 PubMed: 39013239 DOI: 10.1016/j.scr.2024.103492 -
Zhang H, Zhang T, Wang Y, Shi J, Meng Y, Zhang Q, Guo Q, Duan C
Establishment of a transgene-free iPS cell line (SDCHi007-A) from a young patient bearing a ATP1A2 mutation and suffering from Epilepsy
Zhang H et al. Establishment of a transgene-free iPS cell line (SDCHi007-A) from a young patient bearing a ATP1A2 mutation and suffering from Epilepsy. . 2024-09-00. Pubmed ID: 39002250; DOI: 10.1016/j.scr.2024.103490 SDCHi007-A 2024-09-00 2024-09-00 PubMed: 39002250 DOI: 10.1016/j.scr.2024.103490Associated cell lines:
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Meng XY, Sun HF, Zhang YJ, Li WX, Wang DD, Liu DH, Li SM, Wu Y, Li JK, Liu XH, Liu PP, Yang RZ, Li SA, Kang JS
Generation of an induced pluripotent stem cell line (CSBZZUi001-A) from a female Alzheimer's patient carrying the PSEN1 709 T > C heterozygous mutation
Meng XY et al. Generation of an induced pluripotent stem cell line (CSBZZUi001-A) from a female Alzheimer's patient carrying the PSEN1 709 T > C heterozygous mutation. . 2024-09-00. Pubmed ID: 38968760; DOI: 10.1016/j.scr.2024.103486 ZZUi027-AZZUi031-ACSBZZUi001-A 2024-09-00 2024-09-00 PubMed: 38968760 DOI: 10.1016/j.scr.2024.103486Associated cell lines:
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Iqbal Muhammad Khalid, Ambreen Alia, Mujahid Muhammad, Zarlashat Yusra, Abid Muhammad, Yasin Ayesha, Ullah Muhammad Naeem, Shahzad Raheel, Harlina Putri Widyanti, Khan Shahid Ullah, Alissa Mohammed, Algopishi Uthman Balgith, Almubarak Hassan Ali
Cardiomegaly: Navigating the uncharted territories of heart failure - A multimodal radiological journey through advanced imaging, pathophysiological landscapes, and innovative therapeutic frontiers
Iqbal Muhammad Khalid et al. Cardiomegaly: Navigating the uncharted territories of heart failure - A multimodal radiological journey through advanced imaging, pathophysiological landscapes, and innovative therapeutic frontiers. . 2024-09-00. DOI: 10.1016/j.cpcardiol.2024.102748 YCMi005-A 2024-09-00 2024-09-00 DOI: 10.1016/j.cpcardiol.2024.102748Associated cell lines:
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Schuurmans IME, van Karnebeek CDM, Hoogendoorn ADM, Nadif Kasri N, Garanto A
Generation of hiPSC lines from four pyridoxine-dependent epilepsy (PDE) patients carrying the variant c.1279G>C in ALDH7A1 in homozygosis
Schuurmans IME et al. Generation of hiPSC lines from four pyridoxine-dependent epilepsy (PDE) patients carrying the variant c.1279G>C in ALDH7A1 in homozygosis. . 2024-09-00. Pubmed ID: 38936157; DOI: 10.1016/j.scr.2024.103480 SCTCi019-ASCTCi019-BSCTCi026-ASCTCi027-ASCTCi028-ASCTCi029-A 2024-09-00 2024-09-00 PubMed: 38936157 DOI: 10.1016/j.scr.2024.103480Associated cell lines:
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Oliva MK, Bourke J., Kornienko D., Mattei C., Mao M., Kuanyshbek A., Ovchinnikov D., Bryson A., Karle TJ, Maljevic S., Petrou S.
Standardizing a method for functional assessment of neural networks in brain organoids
Oliva MK et al. Standardizing a method for functional assessment of neural networks in brain organoids. . 2024-09-00. DOI: 10.1016/j.jneumeth.2024.110178 WAe009-A-2O 2024-09-00 2024-09-00 DOI: 10.1016/j.jneumeth.2024.110178Associated cell lines:
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Pachernegg S, Robevska G, G A Ferreira L, van den Bergen JA, Vlahos K, Howden SE, Sinclair AH, Ayers KL
Generation of heterozygous (MCRIi031-A-1) and homozygous (MCRIi031-A-2) SOX9 knockout human iPSC lines
Pachernegg S et al. Generation of heterozygous (MCRIi031-A-1) and homozygous (MCRIi031-A-2) SOX9 knockout human iPSC lines. . 2024-09-00. Pubmed ID: 38924973; DOI: 10.1016/j.scr.2024.103484 MCRIi031-AMCRIi031-A-1MCRIi031-A-2 2024-09-00 2024-09-00 PubMed: 38924973 DOI: 10.1016/j.scr.2024.103484Associated cell lines:
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Gong J, Li S, Sun W, Wang P, Han X, Xu C, Chen Y, Yang Y, Luan H, Li R, Wen B, Lv S, Chen R, Guo J, Wei C
Generation of induced pluripotent stem cell line (XWHNi003-A) from a female with APOE gene mutation
Gong J et al. Generation of induced pluripotent stem cell line (XWHNi003-A) from a female with APOE gene mutation. . 2024-09-00. Pubmed ID: 39029293; DOI: 10.1016/j.scr.2024.103501 XWHNi003-A 2024-09-00 2024-09-00 PubMed: 39029293 DOI: 10.1016/j.scr.2024.103501Associated cell lines:
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Juchem M, Lehmann N, Behrens YL, Bär C, Thum T, Hoepfner J
CRISPR/Cas9-based GLA knockout to generate the female Fabry disease human induced pluripotent stem cell line MHHi001-A-15
Juchem M et al. CRISPR/Cas9-based GLA knockout to generate the female Fabry disease human induced pluripotent stem cell line MHHi001-A-15. . 2024-09-00. Pubmed ID: 38905814; DOI: 10.1016/j.scr.2024.103478 MHHi001-AMHHi001-A-15 2024-09-00 2024-09-00 PubMed: 38905814 DOI: 10.1016/j.scr.2024.103478Associated cell lines:
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Hernández D, Morgan Schlicht S, Elli Clarke J, Daniszewski M, Karch CM, Dominantly Inherited Alzheimer Network (DIAN), Goate AM, Pébay A
Generation of a gene-corrected human isogenic iPSC line from an Alzheimer's disease iPSC line carrying the PSEN1 H163R mutation
Hernández D et al. Generation of a gene-corrected human isogenic iPSC line from an Alzheimer's disease iPSC line carrying the PSEN1 H163R mutation. . 2024-09-00. Pubmed ID: 39079290; DOI: 10.1016/j.scr.2024.103495; PMC: PMC11608089 UOMELBi004-A 2024-09-00 2024-09-00 PubMed: 39079290 DOI: 10.1016/j.scr.2024.103495Associated cell lines:
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Wang T, Li Y, Yang C, Yuan H, Na W, Yu S
Generation of iPSC line (FMCPGHi003-A) from human PBMCs of a patient with Familial hemiplegic migraine type 3
Wang T et al. Generation of iPSC line (FMCPGHi003-A) from human PBMCs of a patient with Familial hemiplegic migraine type 3. . 2024-09-00. Pubmed ID: 38880015; DOI: 10.1016/j.scr.2024.103465 FMCPGHi001-AFMCPGHi003-A 2024-09-00 2024-09-00 PubMed: 38880015 DOI: 10.1016/j.scr.2024.103465Associated cell lines:
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Manhas A, Tripathi D, Noishiki C, Wu D, Liu L, Sallam K, Lee JT, Fukaya E, Sayed N
Generation of two iPSC lines from vascular Ehlers-Danlos Syndrome (vEDS) patients carrying a missense mutation in COL3A1 gene
Manhas A et al. Generation of two iPSC lines from vascular Ehlers-Danlos Syndrome (vEDS) patients carrying a missense mutation in COL3A1 gene. . 2024-09-00. Pubmed ID: 38944978; DOI: 10.1016/j.scr.2024.103485; PMC: PMC11315230 BFVSBi003-ABFVSBi004-A 2024-09-00 2024-09-00 PubMed: 38944978 DOI: 10.1016/j.scr.2024.103485Associated cell lines:
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Yammine KM, Mirda Abularach S, Kim SY, Bikovtseva AA, Lilianty J, Butty VL, Schiavoni RP, Bateman JF, Lamandé SR, Shoulders MD
ER procollagen storage defect without coupled unfolded protein response drives precocious arthritis
Yammine KM et al. ER procollagen storage defect without coupled unfolded protein response drives precocious arthritis. . 2024-09-00. Pubmed ID: 38981683; DOI: 10.26508/lsa.202402842; PMC: PMC11234256 MCRIi001-AMCRIi001-A-1MCRIi019-AMCRIi001-BMCRIi019-A-2MCRIi019-A-6MCRIi019-A-7 2024-09-00 2024-09-00 PubMed: 38981683 DOI: 10.26508/lsa.202402842Associated cell lines:
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Gopurappilly R, Musthafa T, Sukumaran S, Viswanath B, Hasan G
Corrigendum to "Generation of feeder-independent transgene-free iPSC lines from a young-onset Parkinson's disease (YOPD) patient with a homozygous PLA2G6: c.2222G>A (p. Arg741Gln) mutation (NCBSi003-A) and unaffected heterozygous parent (NCBSi004-A)" [Stem Cell Res. 67 (2023) 103033]
Gopurappilly R et al. Corrigendum to "Generation of feeder-independent transgene-free iPSC lines from a young-onset Parkinson's disease (YOPD) patient with a homozygous PLA2G6: c.2222G>A (p. Arg741Gln) mutation (NCBSi003-A) and unaffected heterozygous parent (NCBSi004-A)" [Stem Cell Res. 67 (2023) 103033]. . 2024-09-00. Pubmed ID: 39047318; DOI: 10.1016/j.scr.2024.103502 NCBSi003-ANCBSi004-A 2024-09-00 2024-09-00 PubMed: 39047318 DOI: 10.1016/j.scr.2024.103502Associated cell lines:
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Saegusa C, Mutai H, Saeki T, Matsuzaki S, Mizukoshi A, Kitajiri SI, Matsunaga T, Hosoya M, Okano H, Fujioka M
Generation of four induced pluripotent stem cell lines (KEIUi004-A, KEIUi005-A, KEIUi006-A, and KEIUi007-A) from patients with sensorineural hearing loss with mutation in EYA4 gene
Saegusa C et al. Generation of four induced pluripotent stem cell lines (KEIUi004-A, KEIUi005-A, KEIUi006-A, and KEIUi007-A) from patients with sensorineural hearing loss with mutation in EYA4 gene. . 2024-09-00. Pubmed ID: 39002249; DOI: 10.1016/j.scr.2024.103489 KEIUi004-AKEIUi005-AKEIUi006-AKEIUi007-A 2024-09-00 2024-09-00 PubMed: 39002249 DOI: 10.1016/j.scr.2024.103489Associated cell lines:
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Djemai Mohammed, Jalouli Maroua, Chahine Mohamed
Impacts of DCM-linked gating pore currents on the electrophysiological characteristics of hiPSC-CM monolayers
Djemai Mohammed et al. Impacts of DCM-linked gating pore currents on the electrophysiological characteristics of hiPSC-CM monolayers. . 2024-09-00. DOI: 10.1016/j.bbrc.2024.150175 CBRCULi016-ACBRCULi017-ACBRCULi016-A-1 2024-09-00 2024-09-00 DOI: 10.1016/j.bbrc.2024.150175Associated cell lines:
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Pachernegg S, Robevska G, Ferreira LGA, van den Bergen JA, Vlahos K, Howden SE, Sinclair AH, Ayers KL
Generation of a homozygous (MCRIi031-A-3) WT1 knockout human iPSC line
Pachernegg S et al. Generation of a homozygous (MCRIi031-A-3) WT1 knockout human iPSC line. . 2024-09-00. Pubmed ID: 39003885; DOI: 10.1016/j.scr.2024.103494 MCRIi031-AMCRIi031-A-3 2024-09-00 2024-09-00 PubMed: 39003885 DOI: 10.1016/j.scr.2024.103494Associated cell lines:
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Berrocal-Rubio MA, Pawer YDJ, Dinevska M, De Paoli-Iseppi R, Widodo SS, Gleeson J, Rajab N, De Nardo W, Hallab J, Li A, Mantamadiotis T, Clark MB, Wells CA
Discovery of NRG1-VII: the myeloid-derived class of NRG1
Berrocal-Rubio MA et al. Discovery of NRG1-VII: the myeloid-derived class of NRG1. . 2024-08-29. Pubmed ID: 39210279; DOI: 10.1186/s12864-024-10723-2; PMC: PMC11360300 WTSIi018-B 2024-08-29 2024-08-29 PubMed: 39210279 DOI: 10.1186/s12864-024-10723-2Associated cell lines:
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Thimm Chantelle, Adjaye James
Untangling the Uncertain Role of Overactivation of the Renin–Angiotensin–Aldosterone System with the Aging Process Based on Sodium Wasting Human Models
Thimm Chantelle et al. Untangling the Uncertain Role of Overactivation of the Renin–Angiotensin–Aldosterone System with the Aging Process Based on Sodium Wasting Human Models. . 2024-08-28. DOI: 10.3390/ijms25179332 CMCi002-AWMUi021-A 2024-08-28 2024-08-28 DOI: 10.3390/ijms25179332 -
Zanfrini Elisa, Bandral Manuj, Jarc Luka, Ramirez-Torres Maria Alejandra, Pezzolla Daniela, Kufrin Vida, Rodriguez-Aznar Eva, Avila Ana Karen Mojica, Cohrs Christian, Speier Stephan, Neumann Katrin, Gavalas Anthony
Generation and application of novel hES cell reporter lines for the differentiation and maturation of hPS cell-derived islet-like clusters
Zanfrini Elisa et al. Generation and application of novel hES cell reporter lines for the differentiation and maturation of hPS cell-derived islet-like clusters. . 2024-08-27. DOI: 10.1038/s41598-024-69645-4 SCSe001-AHMGUi001-AKSCBi005-AKSCBi005-A-3HMGUi001-A-4SCSe001-A-3HMGUi001-A-8 2024-08-27 2024-08-27 DOI: 10.1038/s41598-024-69645-4Associated cell lines:
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McCulloch Mary Kate, Mehryab Fatemeh, Rashnonejad Afrooz
Navigating the Landscape of CMT1B: Understanding Genetic Pathways, Disease Models, and Potential Therapeutic Approaches
McCulloch Mary Kate et al. Navigating the Landscape of CMT1B: Understanding Genetic Pathways, Disease Models, and Potential Therapeutic Approaches. . 2024-08-26. DOI: 10.3390/ijms25179227 ZJUCHi001-A 2024-08-26 2024-08-26 DOI: 10.3390/ijms25179227Associated cell lines:
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Conteduca Giuseppina, Cangelosi Davide, Baldo Chiara, Arado Alessia, Testa Barbara, Wagner Ryan T., Robertson Keith D., Dequiedt Franck, Fitzsimmons Lane, Malacarne Michela, Filaci Gilberto, Coviello Domenico A.
Impact of NSD1 Alternative Transcripts in Actin Filament Formation and Cellular Division Pathways in Fibroblasts
Conteduca Giuseppina et al. Impact of NSD1 Alternative Transcripts in Actin Filament Formation and Cellular Division Pathways in Fibroblasts. . 2024-08-24. DOI: 10.3390/genes15091117 IGGi003-A 2024-08-24 2024-08-24 DOI: 10.3390/genes15091117Associated cell lines:
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Sleiman Yvonne, Reisqs Jean-Baptiste, Boutjdir Mohamed
Differentiation of Sinoatrial-like Cardiomyocytes as a Biological Pacemaker Model
Sleiman Yvonne et al. Differentiation of Sinoatrial-like Cardiomyocytes as a Biological Pacemaker Model. . 2024-08-23. DOI: 10.3390/ijms25179155 FAMRCi004-AFAMRCi004-BUKMi003-AUKMi004-AUKMi005-A 2024-08-23 2024-08-23 DOI: 10.3390/ijms25179155Associated cell lines:
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Farboud SP, Fathi E, Valipour B, Farahzadi R
Toward the latest advancements in cardiac regeneration using induced pluripotent stem cells (iPSCs) technology: approaches and challenges
Farboud SP et al. Toward the latest advancements in cardiac regeneration using induced pluripotent stem cells (iPSCs) technology: approaches and challenges. . 2024-08-22. Pubmed ID: 39175068; DOI: 10.1186/s12967-024-05499-8; PMC: PMC11342568 YCMi007-A 2024-08-22 2024-08-22 PubMed: 39175068 DOI: 10.1186/s12967-024-05499-8Associated cell lines:
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Lisowski P, Lickfett S, Rybak-Wolf A, Menacho C, Le S, Pentimalli TM, Notopoulou S, Dykstra W, Oehler D, López-Calcerrada S, Mlody B, Otto M, Wu H, Richter Y, Roth P, Anand R, Kulka LAM, Meierhofer D, Glazar P, Legnini I, Telugu NS, Hahn T, Neuendorf N, Miller DC, Böddrich A, Polzin A, Mayatepek E, Diecke S, Olzscha H, Kirstein J, Ugalde C, Petrakis S, Cambridge S, Rajewsky N, Kühn R, Wanker EE, Priller J, Metzger JJ, Prigione A
Mutant huntingtin impairs neurodevelopment in human brain organoids through CHCHD2-mediated neurometabolic failure
Lisowski P et al. Mutant huntingtin impairs neurodevelopment in human brain organoids through CHCHD2-mediated neurometabolic failure. . 2024-08-22. Pubmed ID: 39174523; DOI: 10.1038/s41467-024-51216-w; PMC: PMC11341898 BIHi005-ABIHi033-ABIHi035-AHMGUi001-ABIHi050-ABIHi005-A-24HHUUKDi009-ABIHi288-A 2024-08-22 2024-08-22 PubMed: 39174523 DOI: 10.1038/s41467-024-51216-wAssociated cell lines:
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Enhanced Maturity and Functionality of Vascularized Human Liver Organoids through 3D Bioprinting and Pillar Plate Culture
(unknown author). Enhanced Maturity and Functionality of Vascularized Human Liver Organoids through 3D Bioprinting and Pillar Plate Culture. . 2024-08-22. EDi029-A 2024-08-22 2024-08-22Associated cell lines:
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Iuso Arcangela, Zhang Fangfang, Dorn Tatjana, Gnutti Barbara, Anikster Yair, Kuebler Sarah, Ahrens-Nicklas Rebecca, Gosselin Rachel, Rahman Shamima, Durst Ronen, Zanuttigh Enrica, Güra Miriam, Poch Christine, Meier Anna, Laugwitz Karl-Ludwig, Schüller Hans-Joachim, Messias Ana, Sibon Ody, Finazzi Dario, Rippert Alyssa, Li Dong, Truxal Kristen, Nandi Deipanjan, Lampert Brent, Yeo Mildrid, Gardham Alice, Nissan Batel, Cederboim Smadar Horowitz, Moretti Alessandra
Pantethine ameliorates dilated cardiomyopathy features in PPCS deficiency disorder: evidence from patients and models of the disease
Iuso Arcangela et al. Pantethine ameliorates dilated cardiomyopathy features in PPCS deficiency disorder: evidence from patients and models of the disease. . 2024-08-22. DOI: 10.21203/rs.3.rs-4582436/v1 MRIi001-AMRIi003-AMRIi028-AHMGUi003-A 2024-08-22 2024-08-22 DOI: 10.21203/rs.3.rs-4582436/v1Associated cell lines:
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Shan Y, Zhang Y, Wei Y, Zhang C, Lin H, He J, Wang J, Guo W, Li H, Chen Q, Zhou T, Xing Q, Liu Y, Chen J, Pan G
METTL3/METTL14 maintain human nucleoli integrity by mediating SUV39H1/H2 degradation
Shan Y et al. METTL3/METTL14 maintain human nucleoli integrity by mediating SUV39H1/H2 degradation. . 2024-08-21. Pubmed ID: 39169036; DOI: 10.1038/s41467-024-51742-7; PMC: PMC11339338 WAe001-A 2024-08-21 2024-08-21 PubMed: 39169036 DOI: 10.1038/s41467-024-51742-7Associated cell lines:
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Zhou Wei, Li Huizhong, Song Jinxiu, Suo Feng, Gu Maosheng, Qi Suhua
Healthy Plasma Exosomes Exert Potential Neuroprotective Effects against Methylmalonic Acid-Induced Hippocampal Neuron Injury
Zhou Wei et al. Healthy Plasma Exosomes Exert Potential Neuroprotective Effects against Methylmalonic Acid-Induced Hippocampal Neuron Injury. . 2024-08-21. DOI: 10.1021/acschemneuro.4c00224 SDQLCHi021-A 2024-08-21 2024-08-21 DOI: 10.1021/acschemneuro.4c00224Associated cell lines:
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Grass T, Dokuzluoglu Z, Buchner F, Rosignol I, Thomas J, Caldarelli A, Dalinskaya A, Becker J, Rost F, Marass M, Wirth B, Beyer M, Bonaguro L, Rodriguez-Muela N
Isogenic patient-derived organoids reveal early neurodevelopmental defects in spinal muscular atrophy initiation
Grass T et al. Isogenic patient-derived organoids reveal early neurodevelopmental defects in spinal muscular atrophy initiation. . 2024-08-20. Pubmed ID: 39067446; DOI: 10.1016/j.xcrm.2024.101659; PMC: PMC11384962 HVRDi005-AHVRDi007-AHVRDi015-AHVRDi016-AHVRDi017-ACRTDi004-A 2024-08-20 2024-08-20 PubMed: 39067446 DOI: 10.1016/j.xcrm.2024.101659Associated cell lines:
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Li Yuening, Gray Elizabeth H., Ross Rosie, Zebochin Irene, Lock Amy, Fedele Laura, Kamajaya Louisa Janice, Marrow Rebecca J., Ryan Sarah, Röderer Pascal, Brüstle Oliver, John Susan, Denk Franziska, Taams Leonie S.
Blockade of rheumatoid arthritis synovial fluid-induced sensory neuron activation by JAK inhibitors
Li Yuening et al. Blockade of rheumatoid arthritis synovial fluid-induced sensory neuron activation by JAK inhibitors. . 2024-08-19. DOI: 10.1101/2024.08.19.608613 UKBi013-A 2024-08-19 2024-08-19 DOI: 10.1101/2024.08.19.608613Associated cell lines:
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Matsuo Kinya, Nagamatsu Jun, Nagata Kazuhiro, Umeda Ryusei, Shiota Takaya, Morimoto Satoru, Suzuki Naoki, Aoki Masashi, Okano Hideyuki, Nakamori Masayuki, Nishihara Hideaki
Establishment of a novel amyotrophic lateral sclerosis patient (TARDBPN345K/+)-derived brain microvascular endothelial cell model reveals defective Wnt/β-catenin signaling: investigating diffusion barrier dysfunction and immune cell interaction
Matsuo Kinya et al. Establishment of a novel amyotrophic lateral sclerosis patient (TARDBPN345K/+)-derived brain microvascular endothelial cell model reveals defective Wnt/β-catenin signaling: investigating diffusion barrier dysfunction and immune cell interaction. . 2024-08-15. DOI: 10.3389/fcell.2024.1357204 KEIOi001-A 2024-08-15 2024-08-15 DOI: 10.3389/fcell.2024.1357204Associated cell lines:
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Johnson Omar D., Paul Sayan, Gutierrez Jose A., Russell William K., Ward Michelle C.
DNA damage-associated protein co-expression network in cardiomyocytes informs on tolerance to genetic variation and disease
Johnson Omar D. et al. DNA damage-associated protein co-expression network in cardiomyocytes informs on tolerance to genetic variation and disease. . 2024-08-14. DOI: 10.1101/2024.08.14.607863 WTSIi048-A 2024-08-14 2024-08-14 DOI: 10.1101/2024.08.14.607863Associated cell lines:
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Stüdemann T, Schwarzová B, Schneidewind T, Geertz B, von Bibra C, Nehring M, Rössinger J, Wiegert JS, Eschenhagen T, Weinberger F
Impulse initiation in engrafted pluripotent stem cell-derived cardiomyocytes can stimulate the recipient heart
Stüdemann T et al. Impulse initiation in engrafted pluripotent stem cell-derived cardiomyocytes can stimulate the recipient heart. . 2024-08-13. Pubmed ID: 39059379; DOI: 10.1016/j.stemcr.2024.06.012; PMC: PMC11368679 UKEi001-A 2024-08-13 2024-08-13 PubMed: 39059379 DOI: 10.1016/j.stemcr.2024.06.012Associated cell lines:
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Li Yuening, Lock Amy, Fedele Laura, Zebochin Irene, Sabate Alba, Siddle Matthew, Cainarca Silvia, Röderer Pascal, Montag Katharina, Tarroni Paola, Brüstle Oliver, Shaw Tanya, Taams Leonie, Denk Franziska
Modelling inflammation-induced peripheral sensitization in a dish - more complex than expected?
Li Yuening et al. Modelling inflammation-induced peripheral sensitization in a dish - more complex than expected?. . 2024-08-12. DOI: 10.1101/2024.08.12.607558 UKBi013-A 2024-08-12 2024-08-12 DOI: 10.1101/2024.08.12.607558Associated cell lines:
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Pavlova SV, Shulgina AE, Zakian SM, Dementyeva EV
Studying Pathogenetic Contribution of a Variant of Unknown Significance, p.M659I (c.1977G > A) in MYH7, to the Development of Hypertrophic Cardiomyopathy Using CRISPR/Cas9-Engineered Isogenic Induced Pluripotent Stem Cells
Pavlova SV et al. Studying Pathogenetic Contribution of a Variant of Unknown Significance, p.M659I (c.1977G > A) in MYH7, to the Development of Hypertrophic Cardiomyopathy Using CRISPR/Cas9-Engineered Isogenic Induced Pluripotent Stem Cells. . 2024-08-09. Pubmed ID: 39201382; DOI: 10.3390/ijms25168695; PMC: PMC11354791 ICGi019-AICGi019-BICGi021-AICGi022-AICGi029-AICGi022-A-3ICGi022-A-4ICGi022-A-5ICGi044-BICGi044-CICGi022-A-8 2024-08-09 2024-08-09 PubMed: 39201382 DOI: 10.3390/ijms25168695Associated cell lines:
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Stallmeyer Birgit, Bühlmann Clara, Stakaitis Rytis, Dicke Ann-Kristin, Ghieh Farah, Meier Luisa, Zoch Ansgar, MacKenzie MacLeod David, Steingröver Johanna, Okutman Özlem, Fietz Daniela, Pilatz Adrian, Riera-Escamilla Antoni, Xavier Miguel J., Ruckert Christian, Di Persio Sara, Neuhaus Nina, Gurbuz Ali Sami, Şalvarci Ahmet, Le May Nicolas, McEleny Kevin, Friedrich Corinna, van der Heijden Godfried, Wyrwoll Margot J., Kliesch Sabine, Veltman Joris A., Krausz Csilla, Viville Stéphane, Conrad Donald F., O’Carroll Dónal, Tüttelmann Frank
Inherited defects of piRNA biogenesis cause transposon de-repression, impaired spermatogenesis, and human male infertility
Stallmeyer Birgit et al. Inherited defects of piRNA biogenesis cause transposon de-repression, impaired spermatogenesis, and human male infertility. . 2024-08-09. DOI: 10.1038/s41467-024-50930-9 HUSTi002-A 2024-08-09 2024-08-09 DOI: 10.1038/s41467-024-50930-9Associated cell lines:
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Zhao Yang, Li Citing, Zhou Xiaozhou (Emily)
Chinese learners’ Swahili learning motivational trajectories
Zhao Yang et al. Chinese learners’ Swahili learning motivational trajectories. . 2024-08-08. DOI: 10.1111/ijal.12596 ZJSHDPi001-A 2024-08-08 2024-08-08 DOI: 10.1111/ijal.12596Associated cell lines:
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Alsalloum Almaqdad, Mosin Ilya, Shefer Kristina, Mingaleva Natalia, Kim Alexander, Feoktistova Sofya, Malyugin Boris, Boiko Ernest, Sultanov Shamil, Mityaeva Olga, Volchkov Pavel
Novel and Previously Known Mutations of the KCNV2 Gene Cause Various Variants of the Clinical Course of Cone Dystrophy with Supernormal Rod Response in Children
Alsalloum Almaqdad et al. Novel and Previously Known Mutations of the KCNV2 Gene Cause Various Variants of the Clinical Course of Cone Dystrophy with Supernormal Rod Response in Children. . 2024-08-06. DOI: 10.3390/jcm13164592 ABi001-AABi002-A 2024-08-06 2024-08-06 DOI: 10.3390/jcm13164592 -
Wu Xin-Yi, Lee Yee-Ki, Lau Yee-Man, Au Ka-Wing, Tse Yiu-Lam, Ng Kwong-Man, Wong Chun-Ka, Tse Hung-Fat
The Pathogenic Mechanisms of and Novel Therapies for Lamin A/C-Related Dilated Cardiomyopathy Based on Patient-Specific Pluripotent Stem Cell Platforms and Animal Models
Wu Xin-Yi et al. The Pathogenic Mechanisms of and Novel Therapies for Lamin A/C-Related Dilated Cardiomyopathy Based on Patient-Specific Pluripotent Stem Cell Platforms and Animal Models. . 2024-08-05. DOI: 10.3390/ph17081030 PSMi004-A 2024-08-05 2024-08-05 DOI: 10.3390/ph17081030Associated cell lines:
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Liu Zhonglin, Wang Chunyan, Ni Feng, Li Tingshu, Yang Fenglian, Wei Han, Li Tengyan, Huang Changhui, Wang Junli, Wang Binbin
Identification of a Homozygous Mutation of CCDC40 in a Chinese Infertile Man with MMAF and PCD-like Phenotypes
Liu Zhonglin et al. Identification of a Homozygous Mutation of CCDC40 in a Chinese Infertile Man with MMAF and PCD-like Phenotypes. . 2024-08-01. DOI: 10.1089/gtmb.2023.0263 UHOMi001-A 2024-08-01 2024-08-01 DOI: 10.1089/gtmb.2023.0263Associated cell lines:
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Masano Y, Saegusa C, Ishikawa M, Matsunaga T, Okano H, Fujioka M
Generation of an induced pluripotent stem cell line (KEIUi008-A) from a hearing loss patient with an A1555G mutation in mitochondrial DNA
Masano Y et al. Generation of an induced pluripotent stem cell line (KEIUi008-A) from a hearing loss patient with an A1555G mutation in mitochondrial DNA. . 2024-08-00. Pubmed ID: 38815527; DOI: 10.1016/j.scr.2024.103452 KEIUi008-A 2024-08-00 2024-08-00 PubMed: 38815527 DOI: 10.1016/j.scr.2024.103452Associated cell lines:
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Gao Jingjing, Gunasekar Swetharajan, Xia Ziting, Shalin Kiruba, Jiang Christopher, Chen Hao, Lee Dongtak, Lee Sohyung, Pisal Nishkal D., Luo James N., Griciuc Ana, Karp Jeffrey M., Tanzi Rudolph, Joshi Nitin
Gene therapy for CNS disorders: modalities, delivery and translational challenges
Gao Jingjing et al. Gene therapy for CNS disorders: modalities, delivery and translational challenges. . 2024-08-00. DOI: 10.1038/s41583-024-00829-7 USTCi001-AUSTCi001-A-1KEIUi001-A 2024-08-00 2024-08-00 DOI: 10.1038/s41583-024-00829-7Associated cell lines:
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Casamassa A, Rotundo G, Ceresoni C, Turco EM, Torrente I, Candido O, Nicita F, Tonduti D, Bertini E, Marano M, Ferrari D, Cereda C, Pennuto M, Vescovi AL, Carelli S, Rosati J
Production of an induced pluripotent stem cell line CSSi018-A (14192) from a patient with hypomyelinating leukodystrophy 7 (HLD7) carrying biallelic variants of POLR3A (c.1802 T > A; c.4072G > A)
Casamassa A et al. Production of an induced pluripotent stem cell line CSSi018-A (14192) from a patient with hypomyelinating leukodystrophy 7 (HLD7) carrying biallelic variants of POLR3A (c.1802 T > A; c.4072G > A). . 2024-08-00. Pubmed ID: 38852424; DOI: 10.1016/j.scr.2024.103468 CSSi013-ACSSi018-A 2024-08-00 2024-08-00 PubMed: 38852424 DOI: 10.1016/j.scr.2024.103468 -
Russell Grace C., Hamzaoui Yassin, Rho Daniel, Sutrave Gaurav, Choi Joseph S., Missan Dara S., Reckard Gabrielle A., Gustafson Michael P., Kim Gloria B.
Synthetic biology approaches for enhancing safety and specificity of CAR-T cell therapies for solid cancers
Russell Grace C. et al. Synthetic biology approaches for enhancing safety and specificity of CAR-T cell therapies for solid cancers. . 2024-08-00. DOI: 10.1016/j.jcyt.2024.03.484 SKLRMe002-A 2024-08-00 2024-08-00 DOI: 10.1016/j.jcyt.2024.03.484Associated cell lines:
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Gurwitz David, Steeg Rachel
Enriching iPSC research diversity: Harnessing human biobank collections for improved ethnic representation
Gurwitz David et al. Enriching iPSC research diversity: Harnessing human biobank collections for improved ethnic representation. . 2024-08-00. DOI: 10.1002/ddr.22227 CBRCULi008-ACBRCULi009-A 2024-08-00 2024-08-00 DOI: 10.1002/ddr.22227Associated cell lines:
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Zaki-Dizaji Majid, Abazari Mohammad Foad, Razzaghi Hossein, Shkolnikov Irene, Christie Brian R.
GRM7 deficiency, from excitotoxicity and neuroinflammation to neurodegeneration: Systematic review of GRM7 deficient patients
Zaki-Dizaji Majid et al. GRM7 deficiency, from excitotoxicity and neuroinflammation to neurodegeneration: Systematic review of GRM7 deficient patients. . 2024-08-00. DOI: 10.1016/j.bbih.2024.100808 SDQLCHi014-A 2024-08-00 2024-08-00 DOI: 10.1016/j.bbih.2024.100808Associated cell lines:
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Ye L, Ni B, Wu H, Han X, Li H, Liu J, Hu S, Lei W
Establishment of a human induced pluripotent stem cell line from a patient with dilated cardiomyopathy
Ye L et al. Establishment of a human induced pluripotent stem cell line from a patient with dilated cardiomyopathy. . 2024-08-00. Pubmed ID: 38861774; DOI: 10.1016/j.scr.2024.103467 ICSSUi006-A 2024-08-00 2024-08-00 PubMed: 38861774 DOI: 10.1016/j.scr.2024.103467Associated cell lines:
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Yu Pengfei, Bosholm Carol Christine, Zhu Hainan, Duan Zhongping, Atala Anthony, Zhang Yuanyuan
Beyond waste: understanding urine’s potential in precision medicine
Yu Pengfei et al. Beyond waste: understanding urine’s potential in precision medicine. . 2024-08-00. DOI: 10.1016/j.tibtech.2024.01.009 GIBHi001-ASMBCi013-AKEIOi005-AHHUUKDi011-AHHUUKDi012-ABCRTi007-A 2024-08-00 2024-08-00 DOI: 10.1016/j.tibtech.2024.01.009Associated cell lines:
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Dai Y, Zhu W, Flores Banuelos AG, Li J, Mukherjee S, Algaze C, Wu JC
Generation of two induced pluripotent stem cell lines from patients with Williams syndrome
Dai Y et al. Generation of two induced pluripotent stem cell lines from patients with Williams syndrome. . 2024-08-00. Pubmed ID: 38861775; DOI: 10.1016/j.scr.2024.103460 SCVIi106-ASCVIi107-A 2024-08-00 2024-08-00 PubMed: 38861775 DOI: 10.1016/j.scr.2024.103460Associated cell lines:
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Ren L, Jahng JWS, Belbachir N, Cook Z, Rivero GC, Perez MV, Wu JC
Generation of induced pluripotent stem cell lines from patients with LQT1 caused by heterozygous mutations in the KCNQ1 gene
Ren L et al. Generation of induced pluripotent stem cell lines from patients with LQT1 caused by heterozygous mutations in the KCNQ1 gene. . 2024-08-00. Pubmed ID: 38763038; DOI: 10.1016/j.scr.2024.103443; PMC: PMC11365511 SCVIi110-ASCVIi111-A 2024-08-00 2024-08-00 PubMed: 38763038 DOI: 10.1016/j.scr.2024.103443Associated cell lines:
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Teng Teng, Yang Yuting, Li Huihong, Liu Feng
Toxic effect of fluorene on Perinereis aibuhitensis body wall and its corresponding defense mechanisms: A metabolomics perspective
Teng Teng et al. Toxic effect of fluorene on Perinereis aibuhitensis body wall and its corresponding defense mechanisms: A metabolomics perspective. . 2024-08-00. DOI: 10.1016/j.marpolbul.2024.116674 UCLi024-A 2024-08-00 2024-08-00 DOI: 10.1016/j.marpolbul.2024.116674Associated cell lines:
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Neufeldt D, Schmidt A, Mohr E, Lu D, Chatterjee S, Fuchs M, Xiao K, Pan W, Cushman S, Jahn C, Juchem M, Hunkler HJ, Cipriano G, Jürgens B, Schmidt K, Groß S, Jung M, Hoepfner J, Weber N, Foo R, Pich A, Zweigerdt R, Kraft T, Thum T, Bär C
Circular RNA circZFPM2 regulates cardiomyocyte hypertrophy and survival
Neufeldt D et al. Circular RNA circZFPM2 regulates cardiomyocyte hypertrophy and survival. . 2024-08-00. Pubmed ID: 38639887; DOI: 10.1007/s00395-024-01048-y; PMC: PMC11319402 MHHi001-AMHHi021-AMHHi021-BMHHi001-A-18 2024-08-00 2024-08-00 PubMed: 38639887 DOI: 10.1007/s00395-024-01048-yAssociated cell lines:
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Chen J, Dai T, Li Q, Xu T, Zhang W, Sun J, Liu H
Generation of FOXJ1-EGFP knock-in reporter human embryonic stem cell line, WAe001-A-2D, using CRISPR/Cas9-based gene targeting
Chen J et al. Generation of FOXJ1-EGFP knock-in reporter human embryonic stem cell line, WAe001-A-2D, using CRISPR/Cas9-based gene targeting. . 2024-08-00. Pubmed ID: 38820864; DOI: 10.1016/j.scr.2024.103445 WAe001-AWAe001-A-2D 2024-08-00 2024-08-00 PubMed: 38820864 DOI: 10.1016/j.scr.2024.103445Associated cell lines:
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Pongpaksupasin P, Tong-Ngam P, Jearawiriyapaisarn N, Paiboonsukwong K, Sangkitporn S, Trinavarat A, Tubsuwan A, Atchaneeyasakul LO
Generation of an EYS-associated retinitis pigmentosa patient-derived human pluripotent stem cell line (MUi038-A)
Pongpaksupasin P et al. Generation of an EYS-associated retinitis pigmentosa patient-derived human pluripotent stem cell line (MUi038-A). . 2024-08-00. Pubmed ID: 38810502; DOI: 10.1016/j.scr.2024.103448 MUi031-AMUi032-AMUi038-A 2024-08-00 2024-08-00 PubMed: 38810502 DOI: 10.1016/j.scr.2024.103448 -
Jiamvoraphong N, Lorthongpanich C, Klaihmon P, Kheolamai P, Issaragrisil S
Generation of a human iPSC cell line (MUSIi017-A) from a donor with O negative blood type
Jiamvoraphong N et al. Generation of a human iPSC cell line (MUSIi017-A) from a donor with O negative blood type. . 2024-08-00. Pubmed ID: 38852425; DOI: 10.1016/j.scr.2024.103466 MUSIi017-A 2024-08-00 2024-08-00 PubMed: 38852425 DOI: 10.1016/j.scr.2024.103466Associated cell lines:
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Zhang D, Jennings L, Chen SC, Zaw K, Lamey TM, Thompson JA, McLaren TL, Chen FK, McLenachan S
Establishment of an induced pluripotent stem cell line LEIi019-A from an early-onset retinal dystrophy patient with the autosomal dominant OTX2 c.259G>A variant
Zhang D et al. Establishment of an induced pluripotent stem cell line LEIi019-A from an early-onset retinal dystrophy patient with the autosomal dominant OTX2 c.259G>A variant. . 2024-08-00. Pubmed ID: 38852423; DOI: 10.1016/j.scr.2024.103461 LEIi019-A 2024-08-00 2024-08-00 PubMed: 38852423 DOI: 10.1016/j.scr.2024.103461Associated cell lines:
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Brychka D, Ayala-Nunez NV, Dupas A, Bare Y, Partiot E, Mittelheisser V, Lucansky V, Goetz JG, Osmani N, Gaudin R
Targeting monocytic Occludin impairs transendothelial migration and HIV neuroinvasion
Brychka D et al. Targeting monocytic Occludin impairs transendothelial migration and HIV neuroinvasion. . 2024-08-00. Pubmed ID: 39039298; DOI: 10.1038/s44319-024-00190-x; PMC: PMC11315906 WAe009-A 2024-08-00 2024-08-00 PubMed: 39039298 DOI: 10.1038/s44319-024-00190-xAssociated cell lines:
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Kayser A, Dittmann S, Hamidi J, Laufer SD, Krampe R, Mearini G, Hansen A, Schulze-Bahr E
Generation of a patient-specific hiPS cell line with heterozygous GNB2 mutation (UKMi003-A) causative for human sinus node dysfunction and a corresponding CRISPR/Cas9-corrected isogenic control (UKMi004-A)
Kayser A et al. Generation of a patient-specific hiPS cell line with heterozygous GNB2 mutation (UKMi003-A) causative for human sinus node dysfunction and a corresponding CRISPR/Cas9-corrected isogenic control (UKMi004-A). . 2024-08-00. Pubmed ID: 38776645; DOI: 10.1016/j.scr.2024.103446 UKMi003-AUKMi004-AUKMi005-A 2024-08-00 2024-08-00 PubMed: 38776645 DOI: 10.1016/j.scr.2024.103446 -
Xu Yingxi, Liu Xianbo, Ahmad Muhammad Arslan, Ao Qiang, Yu Yang, Shao Dan, Yu Tianhao
Engineering cell-derived extracellular matrix for peripheral nerve regeneration
Xu Yingxi et al. Engineering cell-derived extracellular matrix for peripheral nerve regeneration. . 2024-08-00. DOI: 10.1016/j.mtbio.2024.101125 IRMBi005-A 2024-08-00 2024-08-00 DOI: 10.1016/j.mtbio.2024.101125Associated cell lines:
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Liu J, Du J, Ma X, Jin Y, Yang Q, Zhai Y, Cheng J, Luan F, Ma M, Zhang Z, Ren Q, Cui H
Generation of an iPSC line from a 79-year-old female patient diagnosed with sporadic Parkinson's disease
Liu J et al. Generation of an iPSC line from a 79-year-old female patient diagnosed with sporadic Parkinson's disease. . 2024-08-00. Pubmed ID: 38820865; DOI: 10.1016/j.scr.2024.103450 HMSCATi003-A 2024-08-00 2024-08-00 PubMed: 38820865 DOI: 10.1016/j.scr.2024.103450Associated cell lines:
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Zhong Wei, Li Dan, Fei Yue, Hong Pan
A review of type 3 Gaucher disease: unique neurological manifestations and advances in treatment
Zhong Wei et al. A review of type 3 Gaucher disease: unique neurological manifestations and advances in treatment. . 2024-08-00. DOI: 10.1007/s13760-024-02493-1 INSAi001-A 2024-08-00 2024-08-00 DOI: 10.1007/s13760-024-02493-1Associated cell lines:
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Wang G, Mao X, Wang W, Wang X, Li S, Wang Z
Bioprinted research models of urological malignancy
Wang G et al. Bioprinted research models of urological malignancy. . 2024-08-00. Pubmed ID: 39175884; DOI: 10.1002/exp.20230126; PMC: PMC11335473 IBPi002-ACHOPi004-A 2024-08-00 2024-08-00 PubMed: 39175884 DOI: 10.1002/exp.20230126Associated cell lines:
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Kudriavskii Viacheslav V., Goncharov Anton O., Eremeev Artem V., Ruchko Evgenii S., Veselovsky Vladimir A., Klimina Ksenia M., Bogomazova Alexandra N., Lagarkova Maria A., Moshkovskii Sergei A., Kliuchnikova Anna A.
RNA Editing by ADAR Adenosine Deaminases in the Cell Models of CAG Repeat Expansion Diseases: Significant Effect of Differentiation from Stem Cells into Brain Organoids in the Absence of Substantial Influence of CAG Repeats on the Level of Editing
Kudriavskii Viacheslav V. et al. RNA Editing by ADAR Adenosine Deaminases in the Cell Models of CAG Repeat Expansion Diseases: Significant Effect of Differentiation from Stem Cells into Brain Organoids in the Absence of Substantial Influence of CAG Repeats on the Level of Editing. . 2024-08-00. DOI: 10.1134/s0006297924080078 RCPCMi008-A 2024-08-00 2024-08-00 DOI: 10.1134/s0006297924080078Associated cell lines:
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Yanick C, Maciel R, Jacobs E, Schatzman J, Shy M, Zuchner S, Saporta M
Generation of 3 patient induced Pluripotent stem cell lines containing SORD mutations linked to a recessive neuropathy
Yanick C et al. Generation of 3 patient induced Pluripotent stem cell lines containing SORD mutations linked to a recessive neuropathy. . 2024-08-00. Pubmed ID: 38796985; DOI: 10.1016/j.scr.2024.103449; PMC: PMC11259078 UMi047-AUMi048-AUMi049-A 2024-08-00 2024-08-00 PubMed: 38796985 DOI: 10.1016/j.scr.2024.103449 -
Zeng Y, Tan X, Xu S, Wang K, Li X, Jiang Y
Generation of an integration-free induced pluripotent stem cell (iPSC) line (SDHI001-A) from a 65-year old adult mitral valve prolapse (MVP) patient
Zeng Y et al. Generation of an integration-free induced pluripotent stem cell (iPSC) line (SDHI001-A) from a 65-year old adult mitral valve prolapse (MVP) patient. . 2024-08-00. Pubmed ID: 38865834; DOI: 10.1016/j.scr.2024.103464 SDHi001-A 2024-08-00 2024-08-00 PubMed: 38865834 DOI: 10.1016/j.scr.2024.103464Associated cell lines:
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Bouwman LF, Joosen MEM, Buijsen RAM, van der Graaf LM, Pepers BA, Voesenek BJB, Brosens E, van de Warrenburg BPC, van Roon-Mom WMC
Generation of human induced pluripotent stem cell lines (LUMCi051-A,B and LUMCi052-A,B,C) of two patients with Spinocerebellar ataxia type 7
Bouwman LF et al. Generation of human induced pluripotent stem cell lines (LUMCi051-A,B and LUMCi052-A,B,C) of two patients with Spinocerebellar ataxia type 7. . 2024-08-00. Pubmed ID: 38851031; DOI: 10.1016/j.scr.2024.103462 LUMCi051-ALUMCi052-ALUMCi051-BLUMCi052-BLUMCi052-C 2024-08-00 2024-08-00 PubMed: 38851031 DOI: 10.1016/j.scr.2024.103462Associated cell lines:
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Gao J, Li J, Xu L, Yan CD, Knowles JW, Wu JC
Generation of two familial hypercholesterolemia patient-specific induced pluripotent stem cell lines harboring heterozygous mutations in the LDLR gene
Gao J et al. Generation of two familial hypercholesterolemia patient-specific induced pluripotent stem cell lines harboring heterozygous mutations in the LDLR gene. . 2024-08-00. Pubmed ID: 38852422; DOI: 10.1016/j.scr.2024.103463; PMC: PMC11532021 SCVIi108-ASCVIi109-A 2024-08-00 2024-08-00 PubMed: 38852422 DOI: 10.1016/j.scr.2024.103463Associated cell lines:
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Yazdani Mazyar
Cellular and Molecular Responses to Mitochondrial DNA Deletions in Kearns-Sayre Syndrome: Some Underlying Mechanisms
Yazdani Mazyar. Cellular and Molecular Responses to Mitochondrial DNA Deletions in Kearns-Sayre Syndrome: Some Underlying Mechanisms. . 2024-08-00. DOI: 10.1007/s12035-024-03938-7 UOMi005-A 2024-08-00 2024-08-00 DOI: 10.1007/s12035-024-03938-7Associated cell lines:
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Yin T, Liao Y, Li X, Wang H, Wu B, Dong X
Characterization of a human induced pluripotent stem cell line (FDCHi015-A) derived from PBMCs of a patient harbouring ALDOB mutation
Yin T et al. Characterization of a human induced pluripotent stem cell line (FDCHi015-A) derived from PBMCs of a patient harbouring ALDOB mutation. . 2024-08-00. Pubmed ID: 38820866; DOI: 10.1016/j.scr.2024.103451 FDCHi015-A 2024-08-00 2024-08-00 PubMed: 38820866 DOI: 10.1016/j.scr.2024.103451Associated cell lines:
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Verma S, Dalabehera S, Maurya R, Singh D, Prasher B, Pandey R, Bapat S, Ramalingam S, Sachidanandan C
Generation of an induced pluripotent stem cell line IGIBi18-A from an Indian patient with Rubinstein Taybi Syndrome
Verma S et al. Generation of an induced pluripotent stem cell line IGIBi18-A from an Indian patient with Rubinstein Taybi Syndrome. . 2024-08-00. Pubmed ID: 38820863; DOI: 10.1016/j.scr.2024.103456 IGIBi018-A 2024-08-00 2024-08-00 PubMed: 38820863 DOI: 10.1016/j.scr.2024.103456Associated cell lines:
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Wang J, Bering J, Alonzo M, Ye S, Texter K, Garg V, Zhao MT
Generation of iPSC line NCHi015-A from a patient with truncus arteriosus carrying heterozygous variants in KMT2D and NOTCH1
Wang J et al. Generation of iPSC line NCHi015-A from a patient with truncus arteriosus carrying heterozygous variants in KMT2D and NOTCH1. . 2024-08-00. Pubmed ID: 38833814; DOI: 10.1016/j.scr.2024.103457; PMC: PMC11193886 NCHi015-A 2024-08-00 2024-08-00 PubMed: 38833814 DOI: 10.1016/j.scr.2024.103457Associated cell lines:
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Brandt Nicola, Köper Franziska, Hausmann Jens, Bräuer Anja U.
Spotlight on plasticity-related genes: Current insights in health and disease
Brandt Nicola et al. Spotlight on plasticity-related genes: Current insights in health and disease. . 2024-08-00. DOI: 10.1016/j.pharmthera.2024.108687 CHWi001-A 2024-08-00 2024-08-00 DOI: 10.1016/j.pharmthera.2024.108687Associated cell lines:
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Lee SH, Lim G, Kim H, Suh D, Choi HK, Kim HP, Yoon HG, Park SW, Kang SM, Kwon C, Oh J, Lee SH
Generation of an induced pluripotent stem cell line from a patient with arrhythmogenic right ventricular cardiomyopathy harboring a TMEM43 splice-site variant
Lee SH et al. Generation of an induced pluripotent stem cell line from a patient with arrhythmogenic right ventricular cardiomyopathy harboring a TMEM43 splice-site variant. . 2024-08-00. Pubmed ID: 38824800; DOI: 10.1016/j.scr.2024.103453 YCMi010-A 2024-08-00 2024-08-00 PubMed: 38824800 DOI: 10.1016/j.scr.2024.103453Associated cell lines:
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Pidishetty D, Maddileti S, Mahato S, Agrawal T, Naik M, Kannabiran C, Jalali S, Mariappan I
Generation and characterization of a Stargardt's disease-specific induced pluripotent stem cell line (LVPEIi008-A) with a homozygous nonsense mutation in exon 44 of ABCA4
Pidishetty D et al. Generation and characterization of a Stargardt's disease-specific induced pluripotent stem cell line (LVPEIi008-A) with a homozygous nonsense mutation in exon 44 of ABCA4. . 2024-08-00. Pubmed ID: 38870564; DOI: 10.1016/j.scr.2024.103458 LVPEIi008-A 2024-08-00 2024-08-00 PubMed: 38870564 DOI: 10.1016/j.scr.2024.103458Associated cell lines:
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Querio G, Antoniotti S, Levi R, Fleischmann BK, Gallo MP, Malan D
Insulin-Activated Signaling Pathway and GLUT4 Membrane Translocation in hiPSC-Derived Cardiomyocytes
Querio G et al. Insulin-Activated Signaling Pathway and GLUT4 Membrane Translocation in hiPSC-Derived Cardiomyocytes. . 2024-07-27. Pubmed ID: 39125765; DOI: 10.3390/ijms25158197; PMC: PMC11312081 UKBi015-B 2024-07-27 2024-07-27 PubMed: 39125765 DOI: 10.3390/ijms25158197Associated cell lines:
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Risato Giovanni, Brañas Casas Raquel, Cason Marco, Bueno Marinas Maria, Pinci Serena, De Gaspari Monica, Visentin Silvia, Rizzo Stefania, Thiene Gaetano, Basso Cristina, Pilichou Kalliopi, Tiso Natascia, Celeghin Rudy
In Vivo Approaches to Understand Arrhythmogenic Cardiomyopathy: Perspectives on Animal Models
Risato Giovanni et al. In Vivo Approaches to Understand Arrhythmogenic Cardiomyopathy: Perspectives on Animal Models. . 2024-07-27. DOI: 10.3390/cells13151264 EURACi004-AHDZi001-A 2024-07-27 2024-07-27 DOI: 10.3390/cells13151264Associated cell lines:
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Zhao Yating, Cai Limeng, Huang Bo, Yin Xiangang, Pan Dan, Dong Jie, Zheng Lei, Chen Hao, Lin Jun, Shou Huafeng, Zhao Zhigang, Jin Lanying, Zhu Xiaoxu, Cai Luya, Zhang Xiaofei, Qian Jianhua
Reappraisal and refined diagnosis of ultrasonography and histological findings for hydatidiform moles: a multicentre retrospective study of 821 patients
Zhao Yating et al. Reappraisal and refined diagnosis of ultrasonography and histological findings for hydatidiform moles: a multicentre retrospective study of 821 patients. . 2024-07-24. DOI: 10.1136/jcp-2024-209638 FAHZUi001-A 2024-07-24 2024-07-24 DOI: 10.1136/jcp-2024-209638Associated cell lines:
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Kogler S, Pedersen GM, Martínez-Ramírez F, Aizenshtadt A, Busek M, Krauss SJK, Wilson SR, Røberg-Larsen H
An FDA-Validated, Self-Cleaning Liquid Chromatography-Mass Spectrometry System for Determining Small-Molecule Drugs and Metabolites in Organoid/Organ-on-Chip Medium
Kogler S et al. An FDA-Validated, Self-Cleaning Liquid Chromatography-Mass Spectrometry System for Determining Small-Molecule Drugs and Metabolites in Organoid/Organ-on-Chip Medium. . 2024-07-23. Pubmed ID: 38985547; DOI: 10.1021/acs.analchem.4c02246; PMC: PMC11270525 HMGUi001-A 2024-07-23 2024-07-23 PubMed: 38985547 DOI: 10.1021/acs.analchem.4c02246Associated cell lines:
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Janssen J, Chirico N, Ainsworth MJ, Cedillo-Servin G, Viola M, Dokter I, Vermonden T, Doevendans PA, Serra M, Voets IK, Malda J, Castilho M, van Laake LW, Sluijter JPG, Sampaio-Pinto V, van Mil A
Hypothermic and cryogenic preservation of cardiac tissue-engineered constructs
Janssen J et al. Hypothermic and cryogenic preservation of cardiac tissue-engineered constructs. . 2024-07-23. Pubmed ID: 38910521; DOI: 10.1039/d3bm01908j; PMC: PMC11265564 UKKi032-CUKKi036-CUKKi037-C 2024-07-23 2024-07-23 PubMed: 38910521 DOI: 10.1039/d3bm01908j -
Wilhelmsen I, Combriat T, Dalmao-Fernandez A, Stokowiec J, Wang C, Olsen PA, Wik JA, Boichuk Y, Aizenshtadt A, Krauss S
The effects of TGF-β-induced activation and starvation of vitamin A and palmitic acid on human stem cell-derived hepatic stellate cells
Wilhelmsen I et al. The effects of TGF-β-induced activation and starvation of vitamin A and palmitic acid on human stem cell-derived hepatic stellate cells. . 2024-07-23. Pubmed ID: 39044210; DOI: 10.1186/s13287-024-03852-8; PMC: PMC11267759 WAe001-AWTSIi046-AHMGUi001-AUCSFi001-A 2024-07-23 2024-07-23 PubMed: 39044210 DOI: 10.1186/s13287-024-03852-8Associated cell lines:
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Zhou Heng, Ye Peng, Xiong Wei, Duan Xingxiang, Jing Shuili, He Yan, Zeng Zhi, Wei Yen, Ye Qingsong
Genome-scale CRISPR-Cas9 screening in stem cells: theories, applications and challenges
Zhou Heng et al. Genome-scale CRISPR-Cas9 screening in stem cells: theories, applications and challenges. . 2024-07-19. DOI: 10.1186/s13287-024-03831-z MUi027-ABCRTi007-A 2024-07-19 2024-07-19 DOI: 10.1186/s13287-024-03831-zAssociated cell lines:
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Kriedemann N, Manstein F, Hernandez-Bautista CA, Ullmann K, Triebert W, Franke A, Mertens M, Stein ICAP, Leffler A, Witte M, Askurava T, Fricke V, Gruh I, Piep B, Kowalski K, Kraft T, Zweigerdt R
Protein-free media for cardiac differentiation of hPSCs in 2000 mL suspension culture
Kriedemann N et al. Protein-free media for cardiac differentiation of hPSCs in 2000 mL suspension culture. . 2024-07-18. Pubmed ID: 39020441; DOI: 10.1186/s13287-024-03826-w; PMC: PMC11256493 MHHi001-AMHHi006-AMHHi008-A 2024-07-18 2024-07-18 PubMed: 39020441 DOI: 10.1186/s13287-024-03826-w -
Budny V, Knöpfli Y, Meier D, Zürcher K, Bodenmann C, Peter SL, Müller T, Tardy M, Cortijo C, Tackenberg C
APOE4 Increases Energy Metabolism in APOE-Isogenic iPSC-Derived Neurons
Budny V et al. APOE4 Increases Energy Metabolism in APOE-Isogenic iPSC-Derived Neurons. . 2024-07-17. Pubmed ID: 39056789; DOI: 10.3390/cells13141207; PMC: PMC11274733 BIONi010-C 2024-07-17 2024-07-17 PubMed: 39056789 DOI: 10.3390/cells13141207Associated cell lines:
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Na Do Hyun, Cui Sheng, Fang Xianying, Lee Hanbi, Eum Sang Hun, Shin Yoo Jin, Lim Sun Woo, Yang Chul Woo, Chung Byung Ha
Advancements in Research on Genetic Kidney Diseases Using Human-Induced Pluripotent Stem Cell-Derived Kidney Organoids
Na Do Hyun et al. Advancements in Research on Genetic Kidney Diseases Using Human-Induced Pluripotent Stem Cell-Derived Kidney Organoids. . 2024-07-13. DOI: 10.3390/cells13141190 CMCi001-ACMCi002-A 2024-07-13 2024-07-13 DOI: 10.3390/cells13141190 -
Neumayer G, Torkelson JL, Li S, McCarthy K, Zhen HH, Vangipuram M, Mader MM, Gebeyehu G, Jaouni TM, Jacków-Malinowska J, Rami A, Hansen C, Guo Z, Gaddam S, Tate KM, Pappalardo A, Li L, Chow GM, Roy KR, Nguyen TM, Tanabe K, McGrath PS, Cramer A, Bruckner A, Bilousova G, Roop D, Tang JY, Christiano A, Steinmetz LM, Wernig M, Oro AE
A scalable and cGMP-compatible autologous organotypic cell therapy for Dystrophic Epidermolysis Bullosa
Neumayer G et al. A scalable and cGMP-compatible autologous organotypic cell therapy for Dystrophic Epidermolysis Bullosa. . 2024-07-11. Pubmed ID: 38992003; DOI: 10.1038/s41467-024-49400-z; PMC: PMC11239819 UCSFi001-A 2024-07-11 2024-07-11 PubMed: 38992003 DOI: 10.1038/s41467-024-49400-zAssociated cell lines:
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Karayol R, Borroto MC, Haghshenas S, Namasivayam A, Reilly J, Levy MA, Relator R, Kerkhof J, McConkey H, Shvedunova M, Petersen AK, Magnussen K, Zweier C, Vasileiou G, Reis A, Savatt JM, Mulligan MR, Bicknell LS, Poke G, Abu-El-Haija A, Duis J, Hannig V, Srivastava S, Barkoudah E, Hauser NS, van den Born M, Hamiel U, Henig N, Baris Feldman H, McKee S, Krapels IPC, Lei Y, Todorova A, Yordanova R, Atemin S, Rogac M, McConnell V, Chassevent A, Barañano KW, Shashi V, Sullivan JA, Peron A, Iascone M, Canevini MP, Friedman J, Reyes IA, Kierstein J, Shen JJ, Ahmed FN, Mao X, Almoguera B, Blanco-Kelly F, Platzer K, Treu AB, Quilichini J, Bourgois A, Chatron N, Januel L, Rougeot C, Carere DA, Monaghan KG, Rousseau J, Myers KA, Sadikovic B, Akhtar A, Campeau PM
MSL2 variants lead to a neurodevelopmental syndrome with lack of coordination, epilepsy, specific dysmorphisms, and a distinct episignature
Karayol R et al. MSL2 variants lead to a neurodevelopmental syndrome with lack of coordination, epilepsy, specific dysmorphisms, and a distinct episignature. . 2024-07-11. Pubmed ID: 38815585; DOI: 10.1016/j.ajhg.2024.05.001; PMC: PMC11267526 ISFi001-A 2024-07-11 2024-07-11 PubMed: 38815585 DOI: 10.1016/j.ajhg.2024.05.001Associated cell lines:
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Zhao Song, Wang Lili, Ouyang Mingyue, Xing Sining, Liu Shuo, Sun Lingyan, Yu Huiying
Polyploid giant cancer cells induced by Docetaxel exhibit a senescence phenotype with the expression of stem cell markers in ovarian cancer cells
Zhao Song et al. Polyploid giant cancer cells induced by Docetaxel exhibit a senescence phenotype with the expression of stem cell markers in ovarian cancer cells. . 2024-07-11. DOI: 10.1371/journal.pone.0306969 SMBCi013-A 2024-07-11 2024-07-11 DOI: 10.1371/journal.pone.0306969Associated cell lines:
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Jothi D., Kulka Linda Anna Michelle
Strategies for modeling aging and age-related diseases
Jothi D. et al. Strategies for modeling aging and age-related diseases. . 2024-07-10. DOI: 10.1038/s41514-024-00161-5 NUIGi035-ANUIGi036-ANUIGi037-AMLUi008-AMLUi009-AMLUi007-JMLUi010-B 2024-07-10 2024-07-10 DOI: 10.1038/s41514-024-00161-5Associated cell lines:
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Khampang S, Lorthongpanich C, Laowtammathron C, Klaihmon P, Meesa S, Suksomboon W, Jiamvoraphong N, Kheolamai P, Luanpitpong S, Easley CA, Mahyari E, Issaragrisil S
The dynamic expression of YAP is essential for the development of male germ cells derived from human embryonic stem cells
Khampang S et al. The dynamic expression of YAP is essential for the development of male germ cells derived from human embryonic stem cells. . 2024-07-08. Pubmed ID: 38977826; DOI: 10.1038/s41598-024-66852-x; PMC: PMC11231333 MUSIe002-AMUSIe002-A-1 2024-07-08 2024-07-08 PubMed: 38977826 DOI: 10.1038/s41598-024-66852-xAssociated cell lines:
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Zhang Huan, Hansen Marten, Di Summa Franca, Von Lindern Marieke, Gillemans Nynke, Van IJcken Wilfred F.J., Svendsen Arthur Flohr, Philipsen Sjaak, Van der Reijden Bert, Varga Eszter, Van den Akker Emile
LSD1/KDM1A and GFI1B repress endothelial fate and induce hematopoietic fate in induced pluripotent stem cell-derived hemogenic endotheliums
Zhang Huan et al. LSD1/KDM1A and GFI1B repress endothelial fate and induce hematopoietic fate in induced pluripotent stem cell-derived hemogenic endotheliums. . 2024-07-04. DOI: 10.3324/haematol.2024.285214 SANi001-ASANi002-ASANi005-A 2024-07-04 2024-07-04 DOI: 10.3324/haematol.2024.285214 -
Feringa Femke M., Koppes-den Hertog Sascha J., Wang Lian, Derks Rico J.E., Kruijff Iris, Erlebach Lena, Heijneman Jorin, Miramontes Ricardo, Pömpner Nadine, Blomberg Niek, Olivier-Jimenez Damien, Johansen Lill Eva, Cammack Alexander J., Giblin Ashling, Toomey Christina E, Rose Indigo V.L., Yuan Hebao, Ward Michael, Isaacs Adrian M., Kampmann Martin, Kronenberg-Versteeg Deborah, Lashley Tammaryn, Thompson Leslie M., Ori Alessandro, Mohammed Yassene, Giera Martin, van der Kant Rik
The Neurolipid Atlas: a lipidomics resource for neurodegenerative diseases uncovers cholesterol as a regulator of astrocyte reactivity impaired by ApoE4
Feringa Femke M. et al. The Neurolipid Atlas: a lipidomics resource for neurodegenerative diseases uncovers cholesterol as a regulator of astrocyte reactivity impaired by ApoE4. . 2024-07-03. DOI: 10.1101/2024.07.01.601474 BIONi037-A 2024-07-03 2024-07-03 DOI: 10.1101/2024.07.01.601474Associated cell lines:
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Stanojević D, Li Z, Bakić S, Foo R, Šikić M
Rockfish: A transformer-based model for accurate 5-methylcytosine prediction from nanopore sequencing
Stanojević D et al. Rockfish: A transformer-based model for accurate 5-methylcytosine prediction from nanopore sequencing. . 2024-07-03. Pubmed ID: 38961062; DOI: 10.1038/s41467-024-49847-0; PMC: PMC11222435 WAe001-A 2024-07-03 2024-07-03 PubMed: 38961062 DOI: 10.1038/s41467-024-49847-0Associated cell lines:
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Puertas-Neyra K, Coco-Martin RM, Hernandez-Rodriguez LA, Gobelli D, Garcia-Ferrer Y, Palma-Vecino R, Tellería JJ, Simarro M, de la Fuente MA, Fernandez-Bueno I
Clinical exome analysis and targeted gene repair of the c.1354dupT variant in iPSC lines from patients with PROM1-related retinopathies exhibiting diverse phenotypes
Puertas-Neyra K et al. Clinical exome analysis and targeted gene repair of the c.1354dupT variant in iPSC lines from patients with PROM1-related retinopathies exhibiting diverse phenotypes. . 2024-07-02. Pubmed ID: 38956727; DOI: 10.1186/s13287-024-03804-2; PMC: PMC11218195 ESi125-AESi126-AESi127-A 2024-07-02 2024-07-02 PubMed: 38956727 DOI: 10.1186/s13287-024-03804-2 -
Benoit Matthieu P. M. H., Rao Lu, Asenjo Ana B., Gennerich Arne, Sosa Hernando
Cryo-EM unveils kinesin KIF1A’s processivity mechanism and the impact of its pathogenic variant P305L
Benoit Matthieu P. M. H. et al. Cryo-EM unveils kinesin KIF1A’s processivity mechanism and the impact of its pathogenic variant P305L. . 2024-07-02. DOI: 10.1038/s41467-024-48720-4 SDUBMSi001-A 2024-07-02 2024-07-02 DOI: 10.1038/s41467-024-48720-4Associated cell lines:
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Fedorenko Alisa V., Khomyakova Ekaterina A., Surdina Anastasia V., Sekretova Elizaveta K., Limanskaya Tatiana V., Belikova Lilia D., Volovikov Egor A., Gridina Maria M., Khabarova Anna A., Kashevarova Anna A., Fedotov Dmitry A., Zerkalenkova Elena A., Lagarkova Maria A., Lebedev Igor N., Bogomazova Alexandra N.
Design of iPSC-based cell model to study the functions of the <i>UBE2A</i> gene
Fedorenko Alisa V. et al. Design of iPSC-based cell model to study the functions of the <i>UBE2A</i> gene. . 2024-07-01. DOI: 10.17816/gc623799 ICGi040-ARCPCMi009-ARCPCMi009-A-1 2024-07-01 2024-07-01 DOI: 10.17816/gc623799Associated cell lines:
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Michalska JM, Lyudchik J, Velicky P, Štefaničková H, Watson JF, Cenameri A, Sommer C, Amberg N, Venturino A, Roessler K, Czech T, Höftberger R, Siegert S, Novarino G, Jonas P, Danzl JG
Imaging brain tissue architecture across millimeter to nanometer scales
Michalska JM et al. Imaging brain tissue architecture across millimeter to nanometer scales. . 2024-07-00. Pubmed ID: 37653226; DOI: 10.1038/s41587-023-01911-8; PMC: PMC11252008 WAe009-A 2024-07-00 2024-07-00 PubMed: 37653226 DOI: 10.1038/s41587-023-01911-8Associated cell lines:
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Klein Alexandra, Klug Katharina, Breyer Maximilian, Grüner Julia, Medala Vijay Krishna, Nordbeck Peter, Wanner Christoph, Klopocki Eva, Üçeyler Nurcan
Genetic variants of unknown significance in alpha‐galactosidase A: Cellular delineation from Fabry disease
Klein Alexandra et al. Genetic variants of unknown significance in alpha‐galactosidase A: Cellular delineation from Fabry disease. . 2024-07-00. DOI: 10.1002/jimd.12743 UKWNLi005-A 2024-07-00 2024-07-00 DOI: 10.1002/jimd.12743Associated cell lines:
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Akter M, Sepehrimanesh M, Xu W, Ding B
Assembling a Coculture System to Prepare Highly Pure Induced Pluripotent Stem Cell-Derived Neurons at Late Maturation Stages
Akter M et al. Assembling a Coculture System to Prepare Highly Pure Induced Pluripotent Stem Cell-Derived Neurons at Late Maturation Stages. . 2024-07-00. Pubmed ID: 39009447; DOI: 10.1523/eneuro.0165-24.2024; PMC: PMC11289586 UCSFi001-A 2024-07-00 2024-07-00 PubMed: 39009447 DOI: 10.1523/eneuro.0165-24.2024Associated cell lines:
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Kwartler Callie S., Esparza Pinelo Jose Emiliano
Use of iPSC-Derived Smooth Muscle Cells to Model Physiology and Pathology
Kwartler Callie S. et al. Use of iPSC-Derived Smooth Muscle Cells to Model Physiology and Pathology. . 2024-07-00. DOI: 10.1161/atvbaha.123.319703 MHHi012-AMHHi013-AMHHi014-ABBANTWi008-ABBANTWi010-A 2024-07-00 2024-07-00 DOI: 10.1161/atvbaha.123.319703Associated cell lines:
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Ribeiro M, Jager J, Furtado M, Carvalho T, Cabral JMS, Brito D, Carmo-Fonseca M, Martins S, da Rocha ST
Generation of induced pluripotent stem cells from an individual with early onset and severe hypertrophic cardiomyopathy linked to MYBPC3: c.772G > A mutation
Ribeiro M et al. Generation of induced pluripotent stem cells from an individual with early onset and severe hypertrophic cardiomyopathy linked to MYBPC3: c.772G > A mutation. . 2024-07-00. Pubmed ID: 38762696; DOI: 10.1007/s13577-024-01073-y; PMC: PMC11194200 EHTJUi003-ASCVIi001-ASCVIi002-AICGi029-AZZUNEUi025-AZZUNEUi028-AIBBISTi009-AIBBISTi009-B 2024-07-00 2024-07-00 PubMed: 38762696 DOI: 10.1007/s13577-024-01073-yAssociated cell lines:
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Roudaut M, Caillaud A, Souguir Z, Bray L, Girardeau A, Rimbert A, Croyal M, Lambert G, Patitucci M, Delpouve G, Vandenhaute É, Le May C, Maubon N, Cariou B, Si-Tayeb K
Human induced pluripotent stem cells-derived liver organoids grown on a Biomimesys® hyaluronic acid-based hydroscaffold as a new model for studying human lipoprotein metabolism
Roudaut M et al. Human induced pluripotent stem cells-derived liver organoids grown on a Biomimesys® hyaluronic acid-based hydroscaffold as a new model for studying human lipoprotein metabolism. . 2024-07-00. Pubmed ID: 39036087; DOI: 10.1002/btm2.10659; PMC: PMC11256179 ITXi001-AITXi012-A 2024-07-00 2024-07-00 PubMed: 39036087 DOI: 10.1002/btm2.10659 -
Martinez‐Montoya Valentina, Sánchez‐Sánchez Luz María, Sandoval‐Pacheco Roberto, Castro Diana Mónica Anaya, Arellano‐Valdez Carmen Araceli, Ávila‐Rejón Carmen Amor, Aguilar‐Juárez Pedro Alejandro, Espino‐Pluma Martín, González‐Santillanes Cruz Antonio, Martínez‐Segovia Rosa Isela, Olmos‐Morfin Dorian, la Torre Ofelia Padilla‐De, Solís‐Sánchez Ishar, Espinosa Mónica Vázquez‐Del Mercado, Villarroel‐Cortés Camilo Ernesto, Velarde‐Félix Jesús Salvador, López‐Valdez Jaime, Olaiz‐Urbina Julio, Ricárdez‐Marcial Edgar, Vergara‐Sánchez Imelda, Radillo‐Díaz Pablo, Kazakova Ekaterina, De la Fuente‐Cortez Beatriz, del Carmen Marquez‐Quiróz Luz, Torres‐Octavo Benjamín, Diaz‐Martinez Rubicel
Mutational spectrum and genotype–phenotype correlation in Mexican patients with infantile‐onset and late‐onset Pompe disease
Martinez‐Montoya Valentina et al. Mutational spectrum and genotype–phenotype correlation in Mexican patients with infantile‐onset and late‐onset Pompe disease. . 2024-07-00. DOI: 10.1002/mgg3.2480 TRNDi007-B 2024-07-00 2024-07-00 DOI: 10.1002/mgg3.2480Associated cell lines:
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Herardot Elise, Liboz Maxime, Lamour Guillaume, Malo Michel, Plancheron Alexandra, Habeler Walter, Geiger Camille, Frank Elie, Campillo Clément, Monville Christelle, Ben M’Barek Karim
Biomechanical Characterization of Retinal Pigment Epitheliums Derived from hPSCs Using Atomic Force Microscopy
Herardot Elise et al. Biomechanical Characterization of Retinal Pigment Epitheliums Derived from hPSCs Using Atomic Force Microscopy. . 2024-07-00. DOI: 10.1007/s12015-024-10717-3 RCe013-A 2024-07-00 2024-07-00 DOI: 10.1007/s12015-024-10717-3Associated cell lines:
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Kriedemann Nils, Triebert Wiebke, Teske Jana, Mertens Mira, Franke Annika, Ullmann Kevin, Manstein Felix, Drakhlis Lika, Haase Alexandra, Halloin Caroline, Martin Ulrich, Zweigerdt Robert
Standardized production of hPSC-derived cardiomyocyte aggregates in stirred spinner flasks
Kriedemann Nils et al. Standardized production of hPSC-derived cardiomyocyte aggregates in stirred spinner flasks. . 2024-07-00. DOI: 10.1038/s41596-024-00976-2 MHHi001-AMHHi001-A-5 2024-07-00 2024-07-00 DOI: 10.1038/s41596-024-00976-2Associated cell lines:
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García-López Marta, Jiménez-Vicente Lydia, González-Jabardo Raquel, Dorado Helena, Gómez-Manjón Irene, Martín Miguel Ángel, Ayuso Carmen, Arenas Joaquín, Gallardo María Esther
Creation of an Isogenic Human iPSC-Based RGC Model of Dominant Optic Atrophy Harboring the Pathogenic Variant c.1861C>T (p.Gln621Ter) in the OPA1 Gene
García-López Marta et al. Creation of an Isogenic Human iPSC-Based RGC Model of Dominant Optic Atrophy Harboring the Pathogenic Variant c.1861C>T (p.Gln621Ter) in the OPA1 Gene. . 2024-06-30. DOI: 10.3390/ijms25137240 IISHDOi001-AIISHDOi006-AIISHDOi007-A 2024-06-30 2024-06-30 DOI: 10.3390/ijms25137240Associated cell lines:
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Olijnik Aude-Anais, Rodriguez-Romera Antonio, Wong Zoë C., Shen Yuqi, Reyat Jasmeet S., Jooss Natalie J., Rayes Julie, Psaila Bethan, Khan Abdullah O.
Generating human bone marrow organoids for disease modeling and drug discovery
Olijnik Aude-Anais et al. Generating human bone marrow organoids for disease modeling and drug discovery. . 2024-07-00. DOI: 10.1038/s41596-024-00971-7 SCTi003-A 2024-07-00 2024-07-00 DOI: 10.1038/s41596-024-00971-7Associated cell lines:
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Goanta Emilia-Violeta, Vacarescu Cristina, Tartea Georgica, Ungureanu Adrian, Militaru Sebastian, Muraretu Alexandra, Faur-Grigori Adelina-Andreea, Petrescu Lucian, Vătăsescu Radu, Cozma Dragos
Unexpected Genetic Twists in Patients with Cardiac Devices
Goanta Emilia-Violeta et al. Unexpected Genetic Twists in Patients with Cardiac Devices. . 2024-06-28. DOI: 10.3390/jcm13133801 HDZi001-A 2024-06-28 2024-06-28 DOI: 10.3390/jcm13133801Associated cell lines:
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Acharya S, Ansari AH, Kumar Das P, Hirano S, Aich M, Rauthan R, Mahato S, Maddileti S, Sarkar S, Kumar M, Phutela R, Gulati S, Rahman A, Goel A, Afzal C, Paul D, Agrawal T, Pulimamidi VK, Jalali S, Nishimasu H, Mariappan I, Nureki O, Maiti S, Chakraborty D
PAM-flexible Engineered FnCas9 variants for robust and ultra-precise genome editing and diagnostics
Acharya S et al. PAM-flexible Engineered FnCas9 variants for robust and ultra-precise genome editing and diagnostics. . 2024-06-28. Pubmed ID: 38942756; DOI: 10.1038/s41467-024-49233-w; PMC: PMC11213958 LVPEIi004-ALVPEIi005-ALVPEIi001-BLVPEIi005-A-1 2024-06-28 2024-06-28 PubMed: 38942756 DOI: 10.1038/s41467-024-49233-wAssociated cell lines:
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Gariballa Nesrin, Mohamed Feda, Badawi Sally, Ali Bassam R.
The double whammy of ER-retention and dominant-negative effects in numerous autosomal dominant diseases: significance in disease mechanisms and therapy
Gariballa Nesrin et al. The double whammy of ER-retention and dominant-negative effects in numerous autosomal dominant diseases: significance in disease mechanisms and therapy. . 2024-06-27. DOI: 10.1186/s12929-024-01054-1 CSUi002-A 2024-06-27 2024-06-27 DOI: 10.1186/s12929-024-01054-1Associated cell lines:
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Ali Eltahir Abdelrazig Mohamed, Smaida Rana, Meyer Morgane, Ou Wenxin, Li Zongjin, Han Zhongchao, Benkirane-Jessel Nadia, Gottenberg Jacques Eric, Hua Guoqiang
iPSCs chondrogenic differentiation for personalized regenerative medicine: a literature review
Ali Eltahir Abdelrazig Mohamed et al. iPSCs chondrogenic differentiation for personalized regenerative medicine: a literature review. . 2024-06-26. DOI: 10.1186/s13287-024-03794-1 MCRIi019-AMCRIi019-A-7 2024-06-26 2024-06-26 DOI: 10.1186/s13287-024-03794-1Associated cell lines:
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Arai Yutaka, Ito Hidenori, Shimizu Tomoya, Shimoda Yuzuno, Song Dan, Matsuo-Takasaki Mami, Hayata Tadayoshi, Hayashi Yohei
Patient-derived and gene-edited pluripotent stem cells lacking NPHP1 recapitulate juvenile nephronophthisis in abnormalities of primary cilia and renal cyst formation
Arai Yutaka et al. Patient-derived and gene-edited pluripotent stem cells lacking NPHP1 recapitulate juvenile nephronophthisis in abnormalities of primary cilia and renal cyst formation. . 2024-06-26. DOI: 10.3389/fcell.2024.1370723 UCSFi001-AUCSFi001-A-68 2024-06-26 2024-06-26 DOI: 10.3389/fcell.2024.1370723Associated cell lines:
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Albuquerque-Wendt Andreia, McCoy Ciaran, Neish Rachel, Dobramysl Ulrich, Beneke Tom, Cowley Sally A., Crouch Kathryn, Wheeler Richard J., Mottram Jeremy C., Gluenz Eva
TransLeish: Identification of membrane transporters essential for survival of intracellularLeishmaniaparasites in a systematic gene deletion screen
Albuquerque-Wendt Andreia et al. TransLeish: Identification of membrane transporters essential for survival of intracellularLeishmaniaparasites in a systematic gene deletion screen. . 2024-06-25. DOI: 10.1101/2024.06.21.600025 STBCi026-ASTBCi044-ASTBCi063-A 2024-06-25 2024-06-25 DOI: 10.1101/2024.06.21.600025Associated cell lines:
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Nebuloni F, Do QB, Cook PR, Walsh EJ, Wade-Martins R
A fluid-walled microfluidic platform for human neuron microcircuits and directed axotomy
Nebuloni F et al. A fluid-walled microfluidic platform for human neuron microcircuits and directed axotomy. . 2024-06-25. Pubmed ID: 38841815; DOI: 10.1039/d4lc00107a; PMC: PMC11198392 STBCi101-A 2024-06-25 2024-06-25 PubMed: 38841815 DOI: 10.1039/d4lc00107aAssociated cell lines:
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Akgün Canan Melis, Cozzitorto Corinna, Sterr Michael, Saber Lama, Setyono Eunike S.A., Wang Xianming, Merl-Pham Juliane, Greisle Tobias, Burtscher Ingo, Lickert Heiko
Resolving human αversusβ cell fate allocation for the generation of stem cell-derived islets
Akgün Canan Melis et al. Resolving human αversusβ cell fate allocation for the generation of stem cell-derived islets. . 2024-06-21. DOI: 10.1101/2024.06.20.599862 HMGUi001-A-46 2024-06-21 2024-06-21 DOI: 10.1101/2024.06.20.599862Associated cell lines:
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Wu HF, Art J, Saini T, Zeltner N
Protocol for generating postganglionic sympathetic neurons using human pluripotent stem cells for electrophysiological and functional assessments
Wu HF et al. Protocol for generating postganglionic sympathetic neurons using human pluripotent stem cells for electrophysiological and functional assessments. . 2024-06-21. Pubmed ID: 38517897; DOI: 10.1016/j.xpro.2024.102970; PMC: PMC10966798 WAe009-A 2024-06-21 2024-06-21 PubMed: 38517897 DOI: 10.1016/j.xpro.2024.102970Associated cell lines:
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İş Özkan, Wang Xue, Reddy Joseph S., Min Yuhao, Yilmaz Elanur, Bhattarai Prabesh, Patel Tulsi, Bergman Jeremiah, Quicksall Zachary, Heckman Michael G., Tutor-New Frederick Q., Can Demirdogen Birsen, White Launia, Koga Shunsuke, Krause Vincent, Inoue Yasuteru, Kanekiyo Takahisa, Cosacak Mehmet Ilyas, Nelson Nastasia, Lee Annie J., Vardarajan Badri, Mayeux Richard, Kouri Naomi, Deniz Kaancan, Carnwath Troy, Oatman Stephanie R., Lewis-Tuffin Laura J., Nguyen Thuy, Carrasquillo Minerva M., Graff-Radford Jonathan, Petersen Ronald C., Jr Jack Clifford R., Kantarci Kejal, Murray Melissa E., Nho Kwangsik, Saykin Andrew J., Dickson Dennis W., Kizil Caghan, Allen Mariet, Ertekin-Taner Nilüfer
Gliovascular transcriptional perturbations in Alzheimer’s disease reveal molecular mechanisms of blood brain barrier dysfunction
İş Özkan et al. Gliovascular transcriptional perturbations in Alzheimer’s disease reveal molecular mechanisms of blood brain barrier dysfunction. . 2024-06-20. DOI: 10.1038/s41467-024-48926-6 ASUi001-AASUi002-AASUi003-AASUi004-AASUi005-AASUi006-A 2024-06-20 2024-06-20 DOI: 10.1038/s41467-024-48926-6 -
Tongkrajang Nongnat, Kobpornchai Porntida, Dubey Pratima, Chaisri Urai, Kulkeaw Kasem
Modelling amoebic brain infection caused by Balamuthia mandrillaris using a human cerebral organoid
Tongkrajang Nongnat et al. Modelling amoebic brain infection caused by Balamuthia mandrillaris using a human cerebral organoid. . 2024-06-20. DOI: 10.1371/journal.pntd.0012274 MUSIi001-A 2024-06-20 2024-06-20 DOI: 10.1371/journal.pntd.0012274Associated cell lines:
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Burton REBECCA, Capel Rebecca, Akerman Emily, Rog-Zielinska Eva, Winbo Annika, Aston Daniel, Mu-u-min Razik, Read Matthew, Bose Samuel, Swietach Pawel, Wang Jingyu, Corbett Alexander, Koschinski Andreas, Montgomery Johanna, Falter Florian, Calamaio Serena, Melgari Dario, Prevostini Rachelle, Rivolta Ilaria, Ayagama Thamali, Jenkin Idan, Simon Jillian, Fakuade Funsho, Pronto Julius, Sharma Parveen, Song Qianqian, Booth Martin, Platt Frances, Lei Ming, Hester Svenja, Fischer Roman, Voigt Niels, Schotten Ulrich, Verheule Sander, Galione Antony, Keller Marco, Bracher Franz, Zaccolo Manuela, Terrar Derek
Lysosomal signalling pathways influence heart rhythm, and regulate atrial function
Burton REBECCA et al. Lysosomal signalling pathways influence heart rhythm, and regulate atrial function. . 2024-06-19. DOI: 10.21203/rs.3.rs-4557026/v1 TMOi001-A 2024-06-19 2024-06-19 DOI: 10.21203/rs.3.rs-4557026/v1Associated cell lines:
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Walsh C, Jin S
Induced Pluripotent Stem Cells and CRISPR-Cas9 Innovations for Treating Alpha-1 Antitrypsin Deficiency and Glycogen Storage Diseases
Walsh C et al. Induced Pluripotent Stem Cells and CRISPR-Cas9 Innovations for Treating Alpha-1 Antitrypsin Deficiency and Glycogen Storage Diseases. . 2024-06-18. Pubmed ID: 38920680; DOI: 10.3390/cells13121052; PMC: PMC11201389 BRCi009-A 2024-06-18 2024-06-18 PubMed: 38920680 DOI: 10.3390/cells13121052Associated cell lines:
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Ackermann M, Saleh F, Abdin SM, Rafiei Hashtchin A, Gensch I, Golgath J, Carvalho Oliveira M, Nguyen AHH, Gaedcke S, Fenske A, Jang MS, Jirmo AC, Abeln M, Hansen G, Lachmann N
Standardized generation of human iPSC-derived hematopoietic organoids and macrophages utilizing a benchtop bioreactor platform under fully defined conditions
Ackermann M et al. Standardized generation of human iPSC-derived hematopoietic organoids and macrophages utilizing a benchtop bioreactor platform under fully defined conditions. . 2024-06-18. Pubmed ID: 38886860; DOI: 10.1186/s13287-024-03785-2; PMC: PMC11184717 MHHi001-ARUCDRi002-AMHHi015-BRUCDRi002-A-38 2024-06-18 2024-06-18 PubMed: 38886860 DOI: 10.1186/s13287-024-03785-2Associated cell lines:
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Li Yang, Ma Ke, Dong Zhujun, Gao Shijuan, Zhang Jing, Huang Shan, Yang Jie, Fang Guangming, Li Yujie, Li Xiaowei, Welch Carrie, Griffin Emily L., Ramaswamy Prema, Valivullah Zaheer, Liu Xiuying, Dong Jianzeng, Wang Dao Wen, Du, Chung Wendy K., Li Yulin
Frameshift variants in C10orf71 cause dilated cardiomyopathy in human, mouse, and organoid models
Li Yang et al. Frameshift variants in C10orf71 cause dilated cardiomyopathy in human, mouse, and organoid models. . 2024-06-17. DOI: 10.1172/jci177172 ZZUNEUi011-AZZUNEUi022-A 2024-06-17 2024-06-17 DOI: 10.1172/jci177172Associated cell lines:
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Zhou Bingna, Gao Peng, Hu Jing, Lin Xiaoyun, Sun Lei, Zhang Qian, Jiang Yan, Wang Ou, Xia Weibo, Xing Xiaoping, Li Mei
Genetic Analysis, Phenotypic Spectrum and Functional Study of Rare Osteogenesis Imperfecta Caused by CRTAP Variants
Zhou Bingna et al. Genetic Analysis, Phenotypic Spectrum and Functional Study of Rare Osteogenesis Imperfecta Caused by CRTAP Variants. . 2024-06-17. DOI: 10.1210/clinem/dgae025 KSCBi006-A 2024-06-17 2024-06-17 DOI: 10.1210/clinem/dgae025Associated cell lines:
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Dobner J, Nguyen T, Pavez-Giani MG, Cyganek L, Distelmaier F, Krutmann J, Prigione A, Rossi A
mtDNA analysis using Mitopore
Dobner J et al. mtDNA analysis using Mitopore. . 2024-06-13. Pubmed ID: 38572068; DOI: 10.1016/j.omtm.2024.101231; PMC: PMC10988129 UMGi176-A 2024-06-13 2024-06-13 PubMed: 38572068 DOI: 10.1016/j.omtm.2024.101231Associated cell lines:
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Altmaier S, Meiser I, Stracke F, Zimmermann H
Diffusion kinetics and perfusion times in tissue models obtained by bioorthogonal Raman μ-spectroscopy
Altmaier S et al. Diffusion kinetics and perfusion times in tissue models obtained by bioorthogonal Raman μ-spectroscopy. . 2024-06-12. Pubmed ID: 38544684; DOI: 10.1016/j.bpr.2024.100150; PMC: PMC10966163 UKKi011-A 2024-06-12 2024-06-12 PubMed: 38544684 DOI: 10.1016/j.bpr.2024.100150Associated cell lines:
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Wang Chencheng, Abadpour Shadab, Aizenshtadt Aleksandra, Dalmao-Fernandez Andrea, Høyem Merete, Wilhelmsen Ingrid, Stokowiec Justyna, Olsen Petter Angell, Krauss Stefan, Chera Simona, Ghila Luiza, Ræder Helge, Scholz Hanne
Cell identity dynamics and insight into insulin secretagogues when employing stem cell-derived islets for disease modeling
Wang Chencheng et al. Cell identity dynamics and insight into insulin secretagogues when employing stem cell-derived islets for disease modeling. . 2024-06-12. DOI: 10.3389/fbioe.2024.1392575 SCSe001-ASCSe001-A-3 2024-06-12 2024-06-12 DOI: 10.3389/fbioe.2024.1392575Associated cell lines:
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Bantounas I, Rooney KM, Lopes FM, Tengku F, Woods S, Zeef LAH, Lin IH, Kuba SY, Bates N, Hummelgaard S, Hillman KA, Cereghini S, Woolf AS, Kimber SJ
Human pluripotent stem cell-derived kidney organoids reveal tubular epithelial pathobiology of heterozygous HNF1B-associated dysplastic kidney malformations
Bantounas I et al. Human pluripotent stem cell-derived kidney organoids reveal tubular epithelial pathobiology of heterozygous HNF1B-associated dysplastic kidney malformations. . 2024-06-11. Pubmed ID: 38788724; DOI: 10.1016/j.stemcr.2024.04.011; PMC: PMC11297557 UMANe002-AUMANe002-A-4UMANe002-A-5UMANCi001-AUMANCi002-AUMANCi003-A 2024-06-11 2024-06-11 PubMed: 38788724 DOI: 10.1016/j.stemcr.2024.04.011Associated cell lines:
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Capel Rebecca A., Akerman Emily, Rog-Zielinska Eva A., Winbo Annika, Aston Daniel, Mu-u-min Razik Bin Abdul, Read Matthew J., Bose Samuel J., Swietach Pawel, Wang Jingyu, Corbett Alexander D., Koschinski Andreas, Falter Florian, Calamaio Serena, Melgari Dario, Prevostini Rachele, Rivolta Ilaria, Ayagama Thamali, Jenkin Ifan, Simon Jillian N., Fakuade Funsho E., Pronto Julius R., Sharma Parveen, Song Qianqian, Booth Martin J, Platt Frances M., Lei Ming, Hester Svenja, Fischer Roman, Voigt Niels, Schotten Ulrich, Verheule Sander, Galione Antony, Keller Marco, Bracher Franz, Zaccolo Manuela, Terrar Derek A., Burton Rebecca A. B.
Lysosomal signalling pathways influence heart rhythm, and regulate atrial function
Capel Rebecca A. et al. Lysosomal signalling pathways influence heart rhythm, and regulate atrial function. . 2024-06-11. DOI: 10.1101/2024.06.10.597905 TMOi001-A 2024-06-11 2024-06-11 DOI: 10.1101/2024.06.10.597905Associated cell lines:
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Tuimebayeva Gulimzhan, Shagrayeva Bibigul, Kerimbayeva Kulyash, Shertayeva Naila, Bitemirova Aliya, Abdurazova Perizat
Developing Multilingual Competence in Future Educators: Approaches, Challenges, and Best Practices
Tuimebayeva Gulimzhan et al. Developing Multilingual Competence in Future Educators: Approaches, Challenges, and Best Practices. . 2024-06-10. DOI: 10.1515/edu-2024-0020 ZJSHDPi001-A 2024-06-10 2024-06-10 DOI: 10.1515/edu-2024-0020Associated cell lines:
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Goncu Beyza, Duzenli Omer Faruk, Yucesan Emrah
Alteration of housekeeping genes and proteins through senescence of human skin fibroblast cells
Goncu Beyza et al. Alteration of housekeeping genes and proteins through senescence of human skin fibroblast cells. . 2024-06-10. DOI: 10.4025/actascibiolsci.v46i1.68465 ISMMSi003-A 2024-06-10 2024-06-10 DOI: 10.4025/actascibiolsci.v46i1.68465Associated cell lines:
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Xu W, Cao Y, Stephens SB, Arredondo MJ, Chen Y, Perez W, Sun L, Yu AC, Kim JJ, Lalani SR, Li N, Horrigan FT, Altamirano F, Wehrens XH, Miyake CY, Zhang L
Folate as a potential treatment for lethal ventricular arrhythmias in TANGO2-deficiency disorder
Xu W et al. Folate as a potential treatment for lethal ventricular arrhythmias in TANGO2-deficiency disorder. . 2024-06-10. Pubmed ID: 38855866; DOI: 10.1172/jci.insight.171005; PMC: PMC11382877 ASUi001-AASUi002-ABCMi002-A 2024-06-10 2024-06-10 PubMed: 38855866 DOI: 10.1172/jci.insight.171005 -
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Systematic optimization of culture media for maintenance of human induced pluripotent stem cells using the response surface methodology
(unknown author). Systematic optimization of culture media for maintenance of human induced pluripotent stem cells using the response surface methodology. . 2024-06-09. UMNi001-A 2024-06-09 2024-06-09Associated cell lines:
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Andrée Birgit, Voß Nils, Kriedemann Nils, Triebert Wiebke, Teske Jana, Mertens Mira, Witte Merlin, Szádocka Sára, Hilfiker Andres, Aper Thomas, Gruh Ina, Zweigerdt Robert
Fabrication of heart tubes from iPSC derived cardiomyocytes and human fibrinogen by rotating mold technology
Andrée Birgit et al. Fabrication of heart tubes from iPSC derived cardiomyocytes and human fibrinogen by rotating mold technology. . 2024-06-07. DOI: 10.1038/s41598-024-64022-7 MHHi001-AMHHi001-A-5 2024-06-07 2024-06-07 DOI: 10.1038/s41598-024-64022-7Associated cell lines:
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Martins-Costa C, Wiegers A, Pham VA, Sidhaye J, Doleschall B, Novatchkova M, Lendl T, Piber M, Peer A, Möseneder P, Stuempflen M, Chow SYA, Seidl R, Prayer D, Höftberger R, Kasprian G, Ikeuchi Y, Corsini NS, Knoblich JA
ARID1B controls transcriptional programs of axon projection in an organoid model of the human corpus callosum
Martins-Costa C et al. ARID1B controls transcriptional programs of axon projection in an organoid model of the human corpus callosum. . 2024-06-06. Pubmed ID: 38718796; DOI: 10.1016/j.stem.2024.04.014 IMBAi001-AIMBAi016-AIMBAi017-AIMBAi001-A-1IMBAi017-A-1IMBAi017-A-2IMBAi017-A-3 2024-06-06 2024-06-06 PubMed: 38718796 DOI: 10.1016/j.stem.2024.04.014Associated cell lines:
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Iwoń Zuzanna, Krogulec Ewelina, Kierlańczyk Aleksandra, Wojasiński Michał, Jastrzębska Elżbieta
Hypoxia and re-oxygenation effects on human cardiomyocytes cultured on polycaprolactone and polyurethane nanofibrous mats
Iwoń Zuzanna et al. Hypoxia and re-oxygenation effects on human cardiomyocytes cultured on polycaprolactone and polyurethane nanofibrous mats. . 2024-06-06. DOI: 10.1186/s13036-024-00432-5 IIMCBi001-AIIMCBi002-A 2024-06-06 2024-06-06 DOI: 10.1186/s13036-024-00432-5Associated cell lines:
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Zaytseva A. K., Perepelina K. I., Kostareva A. A.
Analysis of the role of Na<sub>v</sub>1.5 slow inactivation in the development of inherited cardiac pathology
Zaytseva A. K. et al. Analysis of the role of Na<sub>v</sub>1.5 slow inactivation in the development of inherited cardiac pathology. . 2024-06-05. DOI: 10.31857/s0041377124010052 FAMRCi007-AFAMRCi007-BFAMRCi009-A 2024-06-05 2024-06-05 DOI: 10.31857/s0041377124010052Associated cell lines:
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Wu Zixuan, Li Ling, Xu Tingting, Hu Yi, Peng Xin, Zhang Zheyuan, Yao Xiaolei, Peng Qinghua
Elucidating the multifaceted roles of GPR146 in non-specific orbital inflammation: a concerted analytical approach through the prisms of bioinformatics and machine learning
Wu Zixuan et al. Elucidating the multifaceted roles of GPR146 in non-specific orbital inflammation: a concerted analytical approach through the prisms of bioinformatics and machine learning. . 2024-06-05. DOI: 10.3389/fmed.2024.1309510 ITXi001-AITXi001-A-1 2024-06-05 2024-06-05 DOI: 10.3389/fmed.2024.1309510Associated cell lines:
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Iwoń Z, Krogulec E, Tarnowska I, Łopianiak I, Wojasiński M, Dobrzyń A, Jastrzębska E
Maturation of human cardiomyocytes derived from induced pluripotent stem cells (iPSC-CMs) on polycaprolactone and polyurethane nanofibrous mats
Iwoń Z et al. Maturation of human cardiomyocytes derived from induced pluripotent stem cells (iPSC-CMs) on polycaprolactone and polyurethane nanofibrous mats. . 2024-06-05. Pubmed ID: 38839879; DOI: 10.1038/s41598-024-63905-z; PMC: PMC11153585 IIMCBi001-AIIMCBi002-A 2024-06-05 2024-06-05 PubMed: 38839879 DOI: 10.1038/s41598-024-63905-zAssociated cell lines:
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de Wagenaar Nathalie P, van den Bersselaar Lisa M, Odijk Hanny J H M, Stefens Sanne J M, Reinhardt Dieter P, Roos-Hesselink Jolien W, Kanaar Roland, Verhagen Judith M A, Brüggenwirth Hennie T, van de Laar Ingrid M B H, van der Pluijm Ingrid, Essers Jeroen
Functional analysis of cell lines derived from SMAD3-related Loeys-Dietz syndrome patients provides insights into genotype-phenotype relation
de Wagenaar Nathalie P et al. Functional analysis of cell lines derived from SMAD3-related Loeys-Dietz syndrome patients provides insights into genotype-phenotype relation. . 2024-06-05. DOI: 10.1093/hmg/ddae044 BBANTWi008-A 2024-06-05 2024-06-05 DOI: 10.1093/hmg/ddae044Associated cell lines:
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Ura Hiroki, Niida Yo
Comparison of RNA-Sequencing Methods for Degraded RNA
Ura Hiroki et al. Comparison of RNA-Sequencing Methods for Degraded RNA. . 2024-06-02. DOI: 10.3390/ijms25116143 KMUGMCi001-A 2024-06-02 2024-06-02 DOI: 10.3390/ijms25116143Associated cell lines:
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Jung YH, Ku YA, Moon J, Kim S, Ryu JS, Yoon CH, Chung MH, Kim YH, Kim MK, Kim DH
Efficacy of RCI001 as a therapeutic candidate of dry eye disease in a modified mixed dry eye model
Jung YH et al. Efficacy of RCI001 as a therapeutic candidate of dry eye disease in a modified mixed dry eye model. . 2024-06-01. Pubmed ID: 38822444; DOI: 10.1186/s40662-024-00388-z; PMC: PMC11143567 RCi001-A 2024-06-01 2024-06-01 PubMed: 38822444 DOI: 10.1186/s40662-024-00388-zAssociated cell lines:
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Potdar Chandrakanta, Jagtap Soham, Singh Khushboo, Yadav Ravi, Pal Pramod Kumar, Datta Indrani
Impaired Sonic Hedgehog Responsiveness of Induced Pluripotent Stem Cell-Derived Floor Plate Cells Carrying the LRRK2-I1371V Mutation Contributes to the Ontogenic Origin of Lower Dopaminergic Neuron Yield
Potdar Chandrakanta et al. Impaired Sonic Hedgehog Responsiveness of Induced Pluripotent Stem Cell-Derived Floor Plate Cells Carrying the LRRK2-I1371V Mutation Contributes to the Ontogenic Origin of Lower Dopaminergic Neuron Yield. . 2024-06-01. DOI: 10.1089/scd.2023.0283 IBMSi011-ANIMHi001-ANIMHi004-ANIMHi005-ANIMHi006-A 2024-06-01 2024-06-01 DOI: 10.1089/scd.2023.0283Associated cell lines:
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Grigor'eva EV, Karapetyan LV, Malakhova AA, Medvedev SP, Minina JM, Hayrapetyan VH, Vardanyan VS, Zakian SM, Arakelyan A, Zakharyan R
Generation of iPSCs from a Patient with the M694V Mutation in the MEFV Gene Associated with Familial Mediterranean Fever and Their Differentiation into Macrophages
Grigor'eva EV et al. Generation of iPSCs from a Patient with the M694V Mutation in the MEFV Gene Associated with Familial Mediterranean Fever and Their Differentiation into Macrophages. . 2024-06-01. Pubmed ID: 38892289; DOI: 10.3390/ijms25116102; PMC: PMC11173119 ICGi021-AICGi022-ARAUi001-ARAUi001-BRAUi001-CRAUi002-A 2024-06-01 2024-06-01 PubMed: 38892289 DOI: 10.3390/ijms25116102 -
Liang Liqing, Xu Lei, Dong Qian, Zhang Jing, Qu Mingyi, Yuan Xin, Zeng Quan, Li Huilin, Zhang Bowen, Wang Chao, Fan Tao, He Lijuan, Yue Wen, Xie Xiaoyan, Pei Xuetao
Low Initial Cell Density Promotes the Differentiation and Maturation of Human Pluripotent Stem Cells into Erythrocytes
Liang Liqing et al. Low Initial Cell Density Promotes the Differentiation and Maturation of Human Pluripotent Stem Cells into Erythrocytes. . 2024-06-01. DOI: 10.1089/scd.2023.0204 IHSTMi001-A 2024-06-01 2024-06-01 DOI: 10.1089/scd.2023.0204Associated cell lines:
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Catelli Lucas Ferioli, Mendes da Costa Péricles Natan, Rós Felipe Augusto, Rodrigues Evandra Strazza, Ursoli Fernanda Ferreira, Santos Flávia Leite Souza, Dorigan Mayra, de Castilho Lílian Maria, Covas Dimas Tadeu, Kashima Simone
Highly Defined Induced Pluripotent Stem Cell Lines Mimic Donor Red Blood Cell Antigen Profiles for Therapeutic and Diagnostic Use
Catelli Lucas Ferioli et al. Highly Defined Induced Pluripotent Stem Cell Lines Mimic Donor Red Blood Cell Antigen Profiles for Therapeutic and Diagnostic Use. . 2024-06-01. DOI: 10.1089/cell.2024.0018 KRIBBi001-A 2024-06-01 2024-06-01 DOI: 10.1089/cell.2024.0018Associated cell lines:
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Wang B, Yang L, Gao M, Zhang H, Liu Y, Gai Z
Establishment of a human induced pluripotent stem cell line(SDQLCHi059-A)from a patient with congenital disorder of glycosylation carrying heterozygous mutation in MPI gene
Wang B et al. Establishment of a human induced pluripotent stem cell line(SDQLCHi059-A)from a patient with congenital disorder of glycosylation carrying heterozygous mutation in MPI gene. . 2024-06-00. Pubmed ID: 38493608; DOI: 10.1016/j.scr.2024.103381 SDQLCHi059-A 2024-06-00 2024-06-00 PubMed: 38493608 DOI: 10.1016/j.scr.2024.103381Associated cell lines:
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Wang B, Ren Q, Cui X, Shan W, Guo X, Wang X, Wang J, Li Y, An G
Generation of KCNH2 heterozygous knockout induced pluripotent stem cell (iPSC) line (Long and Short QT Syndrome)
Wang B et al. Generation of KCNH2 heterozygous knockout induced pluripotent stem cell (iPSC) line (Long and Short QT Syndrome). . 2024-06-00. Pubmed ID: 38547667; DOI: 10.1016/j.scr.2024.103400 BJTTHi001-ABJTTHi001-A-4 2024-06-00 2024-06-00 PubMed: 38547667 DOI: 10.1016/j.scr.2024.103400Associated cell lines:
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Bayarsaikhan D, Yoo DH, Lee J, Im YS, Bayarsaikhan G, Kang HA, Kim YO, Lee B
Generation and characterization of GATA6-specific EGFP expressing human induced pluripotent stem cell line, KSCBi017-A-1, using CRISPR/Cas9
Bayarsaikhan D et al. Generation and characterization of GATA6-specific EGFP expressing human induced pluripotent stem cell line, KSCBi017-A-1, using CRISPR/Cas9. . 2024-06-00. Pubmed ID: 38678980; DOI: 10.1016/j.scr.2024.103426 KSCBi017-AKSCBi017-A-1 2024-06-00 2024-06-00 PubMed: 38678980 DOI: 10.1016/j.scr.2024.103426Associated cell lines:
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Peron C, Cavaliere A, Fasano C, Iannielli A, Spagnolo M, Legati A, Nicol Colombo M, Rizzo A, Sciacca FL, Carelli V, Broccoli V, Lamperti C, Tiranti V
Generation of iPSCs from identical twin, one affected by LHON and one unaffected, both carrying a combination of two mitochondrial variants: m.14484 T>C and m.10680G>A
Peron C et al. Generation of iPSCs from identical twin, one affected by LHON and one unaffected, both carrying a combination of two mitochondrial variants: m.14484 T>C and m.10680G>A. . 2024-06-00. Pubmed ID: 38552355; DOI: 10.1016/j.scr.2024.103406 FINCBi001-AHMGUi004-AFINCBi004-AFINCBi005-AFINCBi006-A 2024-06-00 2024-06-00 PubMed: 38552355 DOI: 10.1016/j.scr.2024.103406Associated cell lines:
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Mori M, Yoshii S, Noguchi M, Takagi D, Shimizu T, Ito H, Matsuo-Takasaki M, Nakamura Y, Takahashi S, Hamada H, Ohnuma K, Shiohama T, Hayashi Y
Generation of human induced pluripotent stem cell lines derived from four Rett syndrome patients with MECP2 mutations
Mori M et al. Generation of human induced pluripotent stem cell lines derived from four Rett syndrome patients with MECP2 mutations. . 2024-06-00. Pubmed ID: 38703668; DOI: 10.1016/j.scr.2024.103432 BRCi024-ABRCi025-ABRCi026-ABRCi027-A 2024-06-00 2024-06-00 PubMed: 38703668 DOI: 10.1016/j.scr.2024.103432 -
Ahmad I, Kamai A, Zahra S, Kapoor H, Kumar Srivastava A, Faruq M
Generation and characterization of iPSC lines from Friedreich's ataxia patient (FRDA) with GAA.TTC repeat expansion in the Frataxin (FXN) gene's first intron (IGIBi016-A) and a non-FRDA healthy control individual (IGIBi017-A)
Ahmad I et al. Generation and characterization of iPSC lines from Friedreich's ataxia patient (FRDA) with GAA.TTC repeat expansion in the Frataxin (FXN) gene's first intron (IGIBi016-A) and a non-FRDA healthy control individual (IGIBi017-A). . 2024-06-00. Pubmed ID: 38484450; DOI: 10.1016/j.scr.2024.103382 IGIBi006-AIGIBi008-AIGIBi016-AIGIBi017-A 2024-06-00 2024-06-00 PubMed: 38484450 DOI: 10.1016/j.scr.2024.103382Associated cell lines:
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Palma-Milla Carmen, Prat-Planas Aina, Soengas-Gonda Emma, Centeno-Pla Mónica, Sánchez-Pozo Jaime, Lazaro-Rodriguez Irene, Quesada-Espinosa Juan F., Arteche-Lopez Ana, Olival Jonathan, Pacio-Miguez Marta, Palomares-Bralo María, Santos-Simarro Fernando, Cancho-Candela Ramón, Vázquez-López María, Seidel Veronica, Martinez-Monseny Antonio F., Casas-Alba Didac, Grinberg Daniel, Balcells Susanna, Serrano Mercedes, Rabionet Raquel, Martin Miguel A., Urreizti Roser
Expanding the Phenotypic Spectrum of TRAF7-Related Cardiac, Facial, and Digital Anomalies With Developmental Delay: Report of 11 New Cases and Literature Review
Palma-Milla Carmen et al. Expanding the Phenotypic Spectrum of TRAF7-Related Cardiac, Facial, and Digital Anomalies With Developmental Delay: Report of 11 New Cases and Literature Review. . 2024-06-00. DOI: 10.1016/j.pediatrneurol.2024.03.008 SHCMDLi001-ASHCMDLi002-A 2024-06-00 2024-06-00 DOI: 10.1016/j.pediatrneurol.2024.03.008Associated cell lines:
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Afshar-Saber W, Chen C, Teaney NA, Kim K, Yang Z, Gasparoli FM, Ebrahimi-Fakhari D, Buttermore ED, Pin-Fang Chen I, Pearl PL, Sahin M
Generation and characterization of six human induced pluripotent stem cell lines (hiPSCs) from three individuals with SSADH Deficiency and CRISPR-corrected isogenic controls
Afshar-Saber W et al. Generation and characterization of six human induced pluripotent stem cell lines (hiPSCs) from three individuals with SSADH Deficiency and CRISPR-corrected isogenic controls. . 2024-06-00. Pubmed ID: 38677032; DOI: 10.1016/j.scr.2024.103424; PMC: PMC11178435 BCHi007-ABCHi007-A-1BCHi009-ABCHi009-A-1BCHi011-ABCHi011-A-1 2024-06-00 2024-06-00 PubMed: 38677032 DOI: 10.1016/j.scr.2024.103424Associated cell lines:
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Clayton JS, Vo C, Crane J, Scriba CK, Saker S, Larmonier T, Malfatti E, Romero NB, Ravenscroft G, Laing NG, Taylor RL
Generation of two iPSC lines from patients with inherited central core disease and concurrent malignant hyperthermia caused by dominant missense variants in the RYR1 gene
Clayton JS et al. Generation of two iPSC lines from patients with inherited central core disease and concurrent malignant hyperthermia caused by dominant missense variants in the RYR1 gene. . 2024-06-00. Pubmed ID: 38583293; DOI: 10.1016/j.scr.2024.103410 SCTi003-AHPIi006-AHPIi007-A 2024-06-00 2024-06-00 PubMed: 38583293 DOI: 10.1016/j.scr.2024.103410 -
Lynch AT, Douglas M, Kimber SJ, Birket MJ
The generation and validation of a dual cardiac HAND1-Tomato NKX2-5-GFP human embryonic stem cell line UMANe002-A-3
Lynch AT et al. The generation and validation of a dual cardiac HAND1-Tomato NKX2-5-GFP human embryonic stem cell line UMANe002-A-3. . 2024-06-00. Pubmed ID: 38460234; DOI: 10.1016/j.scr.2024.103342 UMANe002-AUMANe002-A-1UMANe002-A-2UMANe002-A-3 2024-06-00 2024-06-00 PubMed: 38460234 DOI: 10.1016/j.scr.2024.103342Associated cell lines:
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Zhang T, Zhang F, Wang N, Xu T, Zhu L, Chen L, Liu H
Generation of SST-P2A-mCherry reporter human embryonic stem cell line using the CRISPR/Cas9 system (WAe001-A-2C)
Zhang T et al. Generation of SST-P2A-mCherry reporter human embryonic stem cell line using the CRISPR/Cas9 system (WAe001-A-2C). . 2024-06-00. Pubmed ID: 38547668; DOI: 10.1016/j.scr.2024.103397 WAe001-AWAe001-A-2C 2024-06-00 2024-06-00 PubMed: 38547668 DOI: 10.1016/j.scr.2024.103397Associated cell lines:
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Yuan L, Xie M, Tao Y, Chen X, Xu X, Wang X
Generation and characterization of the iPS cell line (SYSUSHi001-A) derived from the peripheral blood mononuclear cells (PBMCs) of a 33-year-old patient with acute myeloid leukemia (AML)
Yuan L et al. Generation and characterization of the iPS cell line (SYSUSHi001-A) derived from the peripheral blood mononuclear cells (PBMCs) of a 33-year-old patient with acute myeloid leukemia (AML). . 2024-06-00. Pubmed ID: 38608356; DOI: 10.1016/j.scr.2024.103360 SYSUSHi001-ASYSUSHi002-A 2024-06-00 2024-06-00 PubMed: 38608356 DOI: 10.1016/j.scr.2024.103360Associated cell lines:
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Gao M, Li X, Lv Y, Yang X, Liu Y, Gai Z
Generation and characterization of an induced pluripotent stem cell (iPSC) line SDQLCHi063-A from peripheral blood mononuclear cells of a patient with Maturity-onset diabetes of the young type 2 carrying GCK exon 1 deletion
Gao M et al. Generation and characterization of an induced pluripotent stem cell (iPSC) line SDQLCHi063-A from peripheral blood mononuclear cells of a patient with Maturity-onset diabetes of the young type 2 carrying GCK exon 1 deletion. . 2024-06-00. Pubmed ID: 38507882; DOI: 10.1016/j.scr.2024.103389 SDQLCHi063-A 2024-06-00 2024-06-00 PubMed: 38507882 DOI: 10.1016/j.scr.2024.103389Associated cell lines:
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Mahato S, Maddileti S, Naik M, Kannabiran C, Jalali S, Mariappan I
Generation of Leber congenital amaurosis, type 12 patient-specific induced pluripotent stem cell line (LVPEIi006-A), harboring a homozygous mutation in RD3
Mahato S et al. Generation of Leber congenital amaurosis, type 12 patient-specific induced pluripotent stem cell line (LVPEIi006-A), harboring a homozygous mutation in RD3. . 2024-06-00. Pubmed ID: 38479331; DOI: 10.1016/j.scr.2024.103380 LVPEIi006-A 2024-06-00 2024-06-00 PubMed: 38479331 DOI: 10.1016/j.scr.2024.103380Associated cell lines:
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Leventoux Nicolas, Morimoto Satoru, Ishikawa Mitsuru, Nakamura Shiho, Ozawa Fumiko, Kobayashi Reona, Watanabe Hirotaka, Supakul Sopak, Okamoto Satoshi, Zhou Zhi, Kobayashi Hiroya, Kato Chris, Hirokawa Yoshifumi, Aiba Ikuko, Takahashi Shinichi, Shibata Shinsuke, Takao Masaki, Yoshida Mari, Endo Fumito, Yamanaka Koji, Kokubo Yasumasa, Okano Hideyuki
Aberrant CHCHD2-associated mitochondriopathy in Kii ALS/PDC astrocytes
Leventoux Nicolas et al. Aberrant CHCHD2-associated mitochondriopathy in Kii ALS/PDC astrocytes. . 2024-06-00. DOI: 10.1007/s00401-024-02734-w KEIOi001-AKEIOi005-A 2024-06-00 2024-06-00 DOI: 10.1007/s00401-024-02734-wAssociated cell lines:
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Luo Pei, Shi Wenjun, Cheng Xianshuo, Yang Jun, Pei Gen, Dong Jian
Which Drugs are More Effective in Preventing Familial Adenomatous Polyposis Progression based on Network Meta-analysis?
Luo Pei et al. Which Drugs are More Effective in Preventing Familial Adenomatous Polyposis Progression based on Network Meta-analysis?. . 2024-06-00. DOI: 10.2174/0113816128289465240422074745 KMUGMCi004-A 2024-06-00 2024-06-00 DOI: 10.2174/0113816128289465240422074745Associated cell lines:
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Xu Wenqing, Chen Keliang, Yuan Yiwen, Guo Min, Dong Qiang, Cui Mei
Ring finger protein 216 loss‐of‐function induces white matter hyperintensities by inhibiting oligodendroglia proliferation
Xu Wenqing et al. Ring finger protein 216 loss‐of‐function induces white matter hyperintensities by inhibiting oligodendroglia proliferation. . 2024-06-00. DOI: 10.1002/cbf.4057 FDHSi003-A 2024-06-00 2024-06-00 DOI: 10.1002/cbf.4057Associated cell lines:
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Clayton JS, Vo C, Crane J, Scriba CK, Saker S, Larmonier T, Malfatti E, Romero NB, Ravenscroft G, Laing NG, Taylor RL
Generation of two iPSC lines from adult central core disease patients with dominant missense variants in the RYR1 gene
Clayton JS et al. Generation of two iPSC lines from adult central core disease patients with dominant missense variants in the RYR1 gene. . 2024-06-00. Pubmed ID: 38582058; DOI: 10.1016/j.scr.2024.103411 SDQLCHi025-ASCTi003-AHPIi008-AHPIi009-A 2024-06-00 2024-06-00 PubMed: 38582058 DOI: 10.1016/j.scr.2024.103411Associated cell lines:
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Danačíková Šárka, Straka Barbora, Daněk Jan, Kořínek Vladimír, Otáhal Jakub
In vitro human cell culture models in a bench‐to‐bedside approach to epilepsy
Danačíková Šárka et al. In vitro human cell culture models in a bench‐to‐bedside approach to epilepsy. . 2024-06-00. DOI: 10.1002/epi4.12941 OGHFUi001-AOGHFUi001-A-1SUTCMi001-A 2024-06-00 2024-06-00 DOI: 10.1002/epi4.12941Associated cell lines:
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Li C, Zhang F, Wang X, Chen M
Generation of a control induced pluripotent stem cell line (SDUCHi001-A) from a healthy male donor
Li C et al. Generation of a control induced pluripotent stem cell line (SDUCHi001-A) from a healthy male donor. . 2024-06-00. Pubmed ID: 38718593; DOI: 10.1016/j.scr.2024.103433 SDQLCHi012-ASDUCHi001-A 2024-06-00 2024-06-00 PubMed: 38718593 DOI: 10.1016/j.scr.2024.103433Associated cell lines:
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Jahn C, Juchem M, Sonnenschein K, Gietz A, Buchegger T, Lachmann N, Göhring G, Behrens YL, Bär C, Thum T, Hoepfner J
Generation of human induced pluripotent stem cell line MHHi029-A from a male Fabry disease patient carrying c.959A > T mutation
Jahn C et al. Generation of human induced pluripotent stem cell line MHHi029-A from a male Fabry disease patient carrying c.959A > T mutation. . 2024-06-00. Pubmed ID: 38552356; DOI: 10.1016/j.scr.2024.103404 MHHi029-A 2024-06-00 2024-06-00 PubMed: 38552356 DOI: 10.1016/j.scr.2024.103404Associated cell lines:
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Liu X, Ishikawa KI, Hattori N, Akamatsu W
Generation of one induced pluripotent stem cell line JUCGRMi004-A from a Charcot-Marie-Tooth disease type 1A (CMT1A) patient with PMP22 duplication
Liu X et al. Generation of one induced pluripotent stem cell line JUCGRMi004-A from a Charcot-Marie-Tooth disease type 1A (CMT1A) patient with PMP22 duplication. . 2024-06-00. Pubmed ID: 38537501; DOI: 10.1016/j.scr.2024.103401 JUCGRMi004-A 2024-06-00 2024-06-00 PubMed: 38537501 DOI: 10.1016/j.scr.2024.103401Associated cell lines:
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Zhu W, Zhou J, Shang L, Zhou Y, Wang Q, Yu Y, Dong L, Mao C, Chu S, Jin W, Li J, Gao J
Generation and characterization of an iPS cell line (PUMCi006-A) from skin fibroblasts of a patient with an M239T mutation in PSEN2 gene
Zhu W et al. Generation and characterization of an iPS cell line (PUMCi006-A) from skin fibroblasts of a patient with an M239T mutation in PSEN2 gene. . 2024-06-00. Pubmed ID: 38531230; DOI: 10.1016/j.scr.2024.103391 PUMCi006-A 2024-06-00 2024-06-00 PubMed: 38531230 DOI: 10.1016/j.scr.2024.103391Associated cell lines:
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Sarkar J, Dhepe S, Shivalkar A, Kuhikar R, More S, Konala VBR, Bhanushali P, Khanna A
Generation of human-induced pluripotent stem cell line from PBMC of healthy donor using integration-free Sendai virus technology
Sarkar J et al. Generation of human-induced pluripotent stem cell line from PBMC of healthy donor using integration-free Sendai virus technology. . 2024-06-00. Pubmed ID: 38547666; DOI: 10.1016/j.scr.2024.103402 YBLi004-A 2024-06-00 2024-06-00 PubMed: 38547666 DOI: 10.1016/j.scr.2024.103402Associated cell lines:
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Ura H, Togi S, Hatanaka H, Niida Y
Establishment of a human induced pluripotent stem cell line, KMUGMCi010-A, from a patient with X-linked Ohdo syndrome bearing missense mutation in the MED12 gene
Ura H et al. Establishment of a human induced pluripotent stem cell line, KMUGMCi010-A, from a patient with X-linked Ohdo syndrome bearing missense mutation in the MED12 gene. . 2024-06-00. Pubmed ID: 38492468; DOI: 10.1016/j.scr.2024.103388 KMUGMCi004-AKMUGMCi009-AKMUGMCi010-A 2024-06-00 2024-06-00 PubMed: 38492468 DOI: 10.1016/j.scr.2024.103388Associated cell lines:
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Xin H, Lv Y, Wei X, Song W, Li Z, Liu Y, Gai Z
Establishment of a non-integrated iPSC (SDQLCHi068-A) line derived from a patient with autosomal dominant immunodeficiency-14A carrying a heterozygous mutation (c.3061G>A) in PIK3CD gene
Xin H et al. Establishment of a non-integrated iPSC (SDQLCHi068-A) line derived from a patient with autosomal dominant immunodeficiency-14A carrying a heterozygous mutation (c.3061G>A) in PIK3CD gene. . 2024-06-00. Pubmed ID: 38507881; DOI: 10.1016/j.scr.2024.103385 SDQLCHi068-A 2024-06-00 2024-06-00 PubMed: 38507881 DOI: 10.1016/j.scr.2024.103385Associated cell lines:
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Dillen L, Fatima N, Hommersom MP, Çepni E, Fatima F, van Beusekom E, Albert S, van Hagen JM, de Vries BBA, Khan AA, de Brouwer APM, van Bokhoven H
Generation of induced pluripotent stem cell lines from two unrelated patients affected by intellectual disability carrying homozygous variants in SGIP1
Dillen L et al. Generation of induced pluripotent stem cell lines from two unrelated patients affected by intellectual disability carrying homozygous variants in SGIP1. . 2024-06-00. Pubmed ID: 38739972; DOI: 10.1016/j.scr.2024.103442 SCTCi034-ASCTCi035-A 2024-06-00 2024-06-00 PubMed: 38739972 DOI: 10.1016/j.scr.2024.103442Associated cell lines:
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Tharehalli Umesh, Rimbert Antoine
G protein-coupled receptor 146: new insights from genetics and model systems
Tharehalli Umesh et al. G protein-coupled receptor 146: new insights from genetics and model systems. . 2024-06-00. DOI: 10.1097/mol.0000000000000929 ITXi001-AITXi001-A-1 2024-06-00 2024-06-00 DOI: 10.1097/mol.0000000000000929Associated cell lines:
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Pasqualotto Bryce A., Tegeman Carina, Frame Ariel K., McPhedrain Ryan, Halangoda Kolitha, Sheldon Claire A., Rintoul Gordon L.
Galactose-replacement unmasks the biochemical consequences of the G11778A mitochondrial DNA mutation of LHON in patient-derived fibroblasts
Pasqualotto Bryce A. et al. Galactose-replacement unmasks the biochemical consequences of the G11778A mitochondrial DNA mutation of LHON in patient-derived fibroblasts. . 2024-06-00. DOI: 10.1016/j.yexcr.2024.114075 FINCBi001-A 2024-06-00 2024-06-00 DOI: 10.1016/j.yexcr.2024.114075Associated cell lines:
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Ruotolo G, D'Anzi A, Casamassa A, Mazzoni M, Ferrari D, Lombardi I, Carletti RM, D'Asdia C, Torrente I, Frezza K, Lattante S, Sabatelli M, Pennuto M, Vescovi AL, Rosati J
Generation of induced pluripotent stem cells (CSSi017-A)(12862) from an ALS patient carrying a repeat expansion in the C9orf72 gene
Ruotolo G et al. Generation of induced pluripotent stem cells (CSSi017-A)(12862) from an ALS patient carrying a repeat expansion in the C9orf72 gene. . 2024-06-00. Pubmed ID: 38613988; DOI: 10.1016/j.scr.2024.103412 CSSi017-A 2024-06-00 2024-06-00 PubMed: 38613988 DOI: 10.1016/j.scr.2024.103412Associated cell lines:
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Zhen Y, He Q, Sun C, Ma Y, Li Q, Wen L
Generate an AZFa deleted human embryonic stem cell line
Zhen Y et al. Generate an AZFa deleted human embryonic stem cell line. . 2024-06-00. Pubmed ID: 38733811; DOI: 10.1016/j.scr.2024.103436 WAe001-A-2F 2024-06-00 2024-06-00 PubMed: 38733811 DOI: 10.1016/j.scr.2024.103436Associated cell lines:
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Veleva D, Ay M, Ovchinnikov DA, Prowse ABJ, Menezes MJ, Nafisinia M
Generation of two lymphoblastoid-derived induced pluripotent stem cell (iPSC) lines from patients with phenylketonuria
Veleva D et al. Generation of two lymphoblastoid-derived induced pluripotent stem cell (iPSC) lines from patients with phenylketonuria. . 2024-06-00. Pubmed ID: 38552357; DOI: 10.1016/j.scr.2024.103407 WIMRi001-AWIMRi002-A 2024-06-00 2024-06-00 PubMed: 38552357 DOI: 10.1016/j.scr.2024.103407Associated cell lines:
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Zhang X, Li Z, Liu Y, Xin H, Gai Z
Establishment of a non-integrated iPSC (SDQLCHi066-A) line derived from Segawa syndrome patients harboring heterozygous mutations in the TH gene (p.G247S and p.D491H)
Zhang X et al. Establishment of a non-integrated iPSC (SDQLCHi066-A) line derived from Segawa syndrome patients harboring heterozygous mutations in the TH gene (p.G247S and p.D491H). . 2024-06-00. Pubmed ID: 38492469; DOI: 10.1016/j.scr.2024.103392 SDQLCHi066-A 2024-06-00 2024-06-00 PubMed: 38492469 DOI: 10.1016/j.scr.2024.103392Associated cell lines:
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Edwards S, Hagenau L, Nowack B, Rhode J, Hossain MF, Tzvetkova A, Jensen LR, Kuss AW
Generation of two isogenic iPSC lines from a healthy male donor of European ancestry
Edwards S et al. Generation of two isogenic iPSC lines from a healthy male donor of European ancestry. . 2024-06-00. Pubmed ID: 38555715; DOI: 10.1016/j.scr.2024.103403 UMGWi004-AUMGWi004-B 2024-06-00 2024-06-00 PubMed: 38555715 DOI: 10.1016/j.scr.2024.103403Associated cell lines:
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Yin X, Cai Y, Jia N, Hui L, Zhu Z
Characterization of the human induced pluripotent stem cell (iPSC) SZGJMSi004-A line from a 28-year-old Han male patient with depression
Yin X et al. Characterization of the human induced pluripotent stem cell (iPSC) SZGJMSi004-A line from a 28-year-old Han male patient with depression. . 2024-06-00. Pubmed ID: 38696853; DOI: 10.1016/j.scr.2024.103428 SZGJMSi004-A 2024-06-00 2024-06-00 PubMed: 38696853 DOI: 10.1016/j.scr.2024.103428Associated cell lines:
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Li X, Ma Y, Huang C, Yang J, Guo M, Xu X, Guo X
Establishing a human-induced pluripotent stem cell line SMUSHi005-A from a patient with hypophosphatemic vitamin D-resistant rickets carrying the PHEX c.1586-1586+1 delAG mutation
Li X et al. Establishing a human-induced pluripotent stem cell line SMUSHi005-A from a patient with hypophosphatemic vitamin D-resistant rickets carrying the PHEX c.1586-1586+1 delAG mutation. . 2024-06-00. Pubmed ID: 38761687; DOI: 10.1016/j.scr.2024.103439 SMUSHi005-A 2024-06-00 2024-06-00 PubMed: 38761687 DOI: 10.1016/j.scr.2024.103439Associated cell lines:
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Alayoubi Abdulfatah M., Khawaji Zakaria Y., Mohammed Mohammed A., Mercier François E.
CRISPR-Cas9 system: a novel and promising era of genotherapy for beta-hemoglobinopathies, hematological malignancy, and hemophilia
Alayoubi Abdulfatah M. et al. CRISPR-Cas9 system: a novel and promising era of genotherapy for beta-hemoglobinopathies, hematological malignancy, and hemophilia. . 2024-06-00. DOI: 10.1007/s00277-023-05457-2 YCMi001-BYCMi001-B-1 2024-06-00 2024-06-00 DOI: 10.1007/s00277-023-05457-2Associated cell lines:
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Frederiksen Henriette Reventlow S., Skov Søren, Tveden-Nyborg Pernille, Freude Kristine, Doehn Ulrik
Novel traceable CRISPR-Cas9 engineered human embryonic stem cell line (E1C3 + hSEAP + 2xKO + pCD47), has potential to evade immune detection in pigs
Frederiksen Henriette Reventlow S. et al. Novel traceable CRISPR-Cas9 engineered human embryonic stem cell line (E1C3 + hSEAP + 2xKO + pCD47), has potential to evade immune detection in pigs. . 2024-06-00. DOI: 10.1016/j.scr.2024.103438 NOVOe002-A 2024-06-00 2024-06-00 DOI: 10.1016/j.scr.2024.103438Associated cell lines:
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Banerjee R, Ghanty R, Jagtap S, Holla V, Kamble N, Yadav R, Pal PK, Datta I
Generation of induced pluripotent stem cells (NIMHi015-A) from a Parkinson's Disease patient harbouring a homozygous Exon 3 deletion in the PRKN gene
Banerjee R et al. Generation of induced pluripotent stem cells (NIMHi015-A) from a Parkinson's Disease patient harbouring a homozygous Exon 3 deletion in the PRKN gene. . 2024-06-00. Pubmed ID: 38739971; DOI: 10.1016/j.scr.2024.103440 NIMHi001-ANIMHi002-ANIMHi003-ANIMHi004-ANIMHi005-ANIMHi006-ANIMHi015-A 2024-06-00 2024-06-00 PubMed: 38739971 DOI: 10.1016/j.scr.2024.103440Associated cell lines:
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Wang Y, Liu W, Yang Y, Wang Y, Tang Y, Zhan Z, Sun X, Jiao Y, Shan D, Zhang R, Wang D, Sun P, Sun X, Yan C, Liu F
Establishment of an induced pluripotent stem cell (iPSC) line (INNDSUi004-A) from a patient with Congenital Nemaline Myopathy
Wang Y et al. Establishment of an induced pluripotent stem cell (iPSC) line (INNDSUi004-A) from a patient with Congenital Nemaline Myopathy. . 2024-06-00. Pubmed ID: 38733812; DOI: 10.1016/j.scr.2024.103435 INNDSUi004-A 2024-06-00 2024-06-00 PubMed: 38733812 DOI: 10.1016/j.scr.2024.103435Associated cell lines:
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Liu W, Wang Y, Yang Y, Wang Y, Tang Y, Jiao Y, Shan D, Zhan Z, Zhang R, Wang D, Sun X, Sun P, Sun X, Yan C, Liu F
Establishment of an induced pluripotent stem cell (iPSC) line (INNDSUi005-A) from a healthy female Chinese Han
Liu W et al. Establishment of an induced pluripotent stem cell (iPSC) line (INNDSUi005-A) from a healthy female Chinese Han. . 2024-06-00. Pubmed ID: 38484449; DOI: 10.1016/j.scr.2024.103386 INNDSUi005-A 2024-06-00 2024-06-00 PubMed: 38484449 DOI: 10.1016/j.scr.2024.103386Associated cell lines:
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Tai Y, Goodrich R, Maldonado M, Ortiz J, Martinez J, Ico G, Ko A, Shih HP, Nam J
Nanofiber-microwell cell culture system for spatially patterned differentiation of pluripotent stem cells in 3D
Tai Y et al. Nanofiber-microwell cell culture system for spatially patterned differentiation of pluripotent stem cells in 3D. . 2024-06-00. Pubmed ID: 38883422; DOI: 10.1016/j.mtbio.2024.101109; PMC: PMC11180340 WAe009-A 2024-06-00 2024-06-00 PubMed: 38883422 DOI: 10.1016/j.mtbio.2024.101109Associated cell lines:
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Binder S, Ramachandran H, Haslinger D, Hildebrandt B, Dobner J, Haarmann-Stemmann T, Chiocchetti A, Rossi A
CRISPR/Cas9-mediated editing of ACTB in induced pluripotent stem cells: A model for investigating human ACTB loss-of-function and genetic adaptive responses
Binder S et al. CRISPR/Cas9-mediated editing of ACTB in induced pluripotent stem cells: A model for investigating human ACTB loss-of-function and genetic adaptive responses. . 2024-06-00. Pubmed ID: 38518401; DOI: 10.1016/j.scr.2024.103395 WTSIi018-BWTSIi018-B-12WTSIi018-B-19WTSIi018-B-20 2024-06-00 2024-06-00 PubMed: 38518401 DOI: 10.1016/j.scr.2024.103395Associated cell lines:
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Gao Y, Cheng Y, Lin B, Xiao D, Wen J, Xu J, Zheng R, Zhang M, Cai C, Hu J
Efficient generation of induced pluripotent stem cell lines from healthy donors' peripheral blood mononuclear cells of different genders
Gao Y et al. Efficient generation of induced pluripotent stem cell lines from healthy donors' peripheral blood mononuclear cells of different genders. . 2024-06-00. Pubmed ID: 38636268; DOI: 10.1016/j.scr.2024.103421 SZBKi003-ASZBKi004-ASZBKi005-A 2024-06-00 2024-06-00 PubMed: 38636268 DOI: 10.1016/j.scr.2024.103421Associated cell lines:
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Léger Laurens, De Clercq Chloë, Aalders Jeffrey, Van Acker-Verberckt Kiara, Braeckmans Kevin, van Hengel Jolanda
Photoporation-mediated spatial intracellular delivery of stem cell-derived cardiomyocytes
Léger Laurens et al. Photoporation-mediated spatial intracellular delivery of stem cell-derived cardiomyocytes. . 2024-06-00. DOI: 10.1016/j.mex.2024.102548 UGENTi001-A 2024-06-00 2024-06-00 DOI: 10.1016/j.mex.2024.102548Associated cell lines:
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Lee Y, Jeong D, Ham S, Son J, Ko K
Generation of integration-free human induced pluripotent stem cells from a patient with sporadic Parkinson's disease
Lee Y et al. Generation of integration-free human induced pluripotent stem cells from a patient with sporadic Parkinson's disease. . 2024-06-00. Pubmed ID: 38615589; DOI: 10.1016/j.scr.2024.103416 KKUi002-A 2024-06-00 2024-06-00 PubMed: 38615589 DOI: 10.1016/j.scr.2024.103416Associated cell lines:
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Pidishetty D, Maddileti S, Mahato S, Agrawal T, Pulimamidi VK, Naik M, Kannabiran C, Jalali S, Mariappan I
Generation of two induced pluripotent stem cell lines (LVPEIi007-B, LVPEIi008-B) from patients harboring homozygous mutation in ABCA4 (c.6088C>T) using non-integrative Sendai virus-based approach
Pidishetty D et al. Generation of two induced pluripotent stem cell lines (LVPEIi007-B, LVPEIi008-B) from patients harboring homozygous mutation in ABCA4 (c.6088C>T) using non-integrative Sendai virus-based approach. . 2024-06-00. Pubmed ID: 38615588; DOI: 10.1016/j.scr.2024.103418 LVPEIi007-BLVPEIi008-B 2024-06-00 2024-06-00 PubMed: 38615588 DOI: 10.1016/j.scr.2024.103418Associated cell lines:
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Eintracht Jonathan, Owen Nicholas, Harding Philippa, Moosajee Mariya
Disruption of common ocular developmental pathways in patient-derived optic vesicle models of microphthalmia
Eintracht Jonathan et al. Disruption of common ocular developmental pathways in patient-derived optic vesicle models of microphthalmia. . 2024-06-00. DOI: 10.1016/j.stemcr.2024.05.001 UCLi013-AUCLi016-AUCLi017-A 2024-06-00 2024-06-00 DOI: 10.1016/j.stemcr.2024.05.001 -
Maddileti S, Mahato S, Agrawal T, Pravin Dave V, Naik M, Javed Ali M, Kannabiran C, Jalali S, Jayandharan GR, Mariappan I
Generation of two induced pluripotent stem cell lines (LVPEIi004-A and LVPEIi005-A) from probands with Leber Congenital Amaurosis 2 (LCA2) and harboring mutations in RPE65
Maddileti S et al. Generation of two induced pluripotent stem cell lines (LVPEIi004-A and LVPEIi005-A) from probands with Leber Congenital Amaurosis 2 (LCA2) and harboring mutations in RPE65. . 2024-06-00. Pubmed ID: 38631180; DOI: 10.1016/j.scr.2024.103413 LVPEIi004-ALVPEIi005-A 2024-06-00 2024-06-00 PubMed: 38631180 DOI: 10.1016/j.scr.2024.103413Associated cell lines:
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Luo Y, Zheng W, Zhong Y, Liu H, Yu J, Qiu B, Liu J, Yang B
Generation of a human embryonic stem cell line (SMUDHe010-A-1A) carrying Brainbow cassette in the AAVS1 gene by CRISPR/Cas9-mediated homologous recombination
Luo Y et al. Generation of a human embryonic stem cell line (SMUDHe010-A-1A) carrying Brainbow cassette in the AAVS1 gene by CRISPR/Cas9-mediated homologous recombination. . 2024-06-00. Pubmed ID: 38507883; DOI: 10.1016/j.scr.2024.103383 WAe009-A-1A 2024-06-00 2024-06-00 PubMed: 38507883 DOI: 10.1016/j.scr.2024.103383Associated cell lines:
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Hatim O, Xu M, Pavlinov I, Linask K, Beers J, Zou J, Liu C, Rodems S, Baumgärtel K, Gilbert MA, Spinner NB, Chen C, Zheng W
Generation of an Alagille Syndrome (ALGS) patient-derived induced pluripotent stem cell line (TRNDi036-A) carrying a heterozygous mutation (p.Cys693*) in the JAG1 gene
Hatim O et al. Generation of an Alagille Syndrome (ALGS) patient-derived induced pluripotent stem cell line (TRNDi036-A) carrying a heterozygous mutation (p.Cys693*) in the JAG1 gene. . 2024-06-00. Pubmed ID: 38703666; DOI: 10.1016/j.scr.2024.103429; PMC: PMC11144073 TRNDi032-ATRNDi036-A 2024-06-00 2024-06-00 PubMed: 38703666 DOI: 10.1016/j.scr.2024.103429Associated cell lines:
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Cho YK, Kim HK, Suh EJ, Kim HO, Kim S
Generation of a human induced pluripotent stem cell line (YUCMi020-A) from peripheral blood mononuclear cells derived from a female with the Jr(a-) blood type
Cho YK et al. Generation of a human induced pluripotent stem cell line (YUCMi020-A) from peripheral blood mononuclear cells derived from a female with the Jr(a-) blood type. . 2024-06-00. Pubmed ID: 38703667; DOI: 10.1016/j.scr.2024.103434 YUCMi020-A 2024-06-00 2024-06-00 PubMed: 38703667 DOI: 10.1016/j.scr.2024.103434Associated cell lines:
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Wang Y, Wei C, Liu Y, Lu X, Wang W, Song N, Zhang W, Xu J, Zhang W, Han F
Generation of an induced pluripotent stem cell (iPSC) line from a Parkinson's disease patient with a pathogenic LRP10/c.688C > T(p.Arg230Trp) mutation
Wang Y et al. Generation of an induced pluripotent stem cell (iPSC) line from a Parkinson's disease patient with a pathogenic LRP10/c.688C > T(p.Arg230Trp) mutation. . 2024-06-00. Pubmed ID: 38460235; DOI: 10.1016/j.scr.2024.103359 LCPHi003-A 2024-06-00 2024-06-00 PubMed: 38460235 DOI: 10.1016/j.scr.2024.103359Associated cell lines:
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Hou X, Mu J
Generation of a TBX20 homozygous knockout stem cell line (WAe009-A-1E) by episomal vector-based CRISPR/Cas9 system
Hou X et al. Generation of a TBX20 homozygous knockout stem cell line (WAe009-A-1E) by episomal vector-based CRISPR/Cas9 system. . 2024-06-00. Pubmed ID: 38479330; DOI: 10.1016/j.scr.2024.103384 WAe009-AWAe009-A-36WAe009-A-1E 2024-06-00 2024-06-00 PubMed: 38479330 DOI: 10.1016/j.scr.2024.103384Associated cell lines:
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Haidar M, Schmid B, Ruiz A, Ebneth A, Cabrera-Socorro A
Generation of three isogenic, gene-edited iPSC lines carrying the APOE-Christchurch mutation into the three common APOE variants: APOE2Ch, APOE3Ch and APOE4Ch
Haidar M et al. Generation of three isogenic, gene-edited iPSC lines carrying the APOE-Christchurch mutation into the three common APOE variants: APOE2Ch, APOE3Ch and APOE4Ch. . 2024-06-00. Pubmed ID: 38703665; DOI: 10.1016/j.scr.2024.103414 BIONi010-C-70BIONi010-C-71BIONi010-C-72 2024-06-00 2024-06-00 PubMed: 38703665 DOI: 10.1016/j.scr.2024.103414Associated cell lines:
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Zaitseva A. K., Perepelina K. I., Kostareva A. A.
Analysis of Slow Inactivation of Nav1.5 Channels in the Development of Hereditary Heart Pathology
Zaitseva A. K. et al. Analysis of Slow Inactivation of Nav1.5 Channels in the Development of Hereditary Heart Pathology. . 2024-06-00. DOI: 10.1134/s1990519x24700263 FAMRCi007-AFAMRCi007-BFAMRCi009-A 2024-06-00 2024-06-00 DOI: 10.1134/s1990519x24700263Associated cell lines:
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Tonin R, Feo F, Falliano S, Giunti L, Calamai M, Procopio E, Mari F, Sciruicchio V, Conti V, Fanelli I, Bambi F, Guerrini R, Morrone A
Generation of a human induced pluripotent stem cell line from a patient with GM3 synthase deficiency using self-replicating RNA vector
Tonin R et al. Generation of a human induced pluripotent stem cell line from a patient with GM3 synthase deficiency using self-replicating RNA vector. . 2024-06-00. Pubmed ID: 38703669; DOI: 10.1016/j.scr.2024.103431 AOUMEYi002-A 2024-06-00 2024-06-00 PubMed: 38703669 DOI: 10.1016/j.scr.2024.103431Associated cell lines:
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Chen X, Sun J, Wang T, Tang Q, Su L, Sun Y, Chen L, Seo H, Cheng T, Wang J, Song B
Generation of a human iPSC line from a Parkinson's disease patient with a novel CHCHD2 mutation (p.R145Q)
Chen X et al. Generation of a human iPSC line from a Parkinson's disease patient with a novel CHCHD2 mutation (p.R145Q). . 2024-06-00. Pubmed ID: 38631182; DOI: 10.1016/j.scr.2024.103419 FDHSi002-A 2024-06-00 2024-06-00 PubMed: 38631182 DOI: 10.1016/j.scr.2024.103419Associated cell lines:
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Korneck M, Leonhardt A, Schöls L, Hauser S
Generation of homozygous and heterozygous REEP1 knockout induced pluripotent stem cell lines by CRISPR/Cas9 gene editing
Korneck M et al. Generation of homozygous and heterozygous REEP1 knockout induced pluripotent stem cell lines by CRISPR/Cas9 gene editing. . 2024-06-00. Pubmed ID: 38479332; DOI: 10.1016/j.scr.2024.103378 HIHCNi008-A-3HIHCNi008-A-4 2024-06-00 2024-06-00 PubMed: 38479332 DOI: 10.1016/j.scr.2024.103378Associated cell lines:
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Guo X, Zhao K, Zhang Y, Zhou T, Pan G
Generation of a PPM1A-deficient human induced pluripotent stem cell line using CRISPR-Cas9 technology
Guo X et al. Generation of a PPM1A-deficient human induced pluripotent stem cell line using CRISPR-Cas9 technology. . 2024-06-00. Pubmed ID: 38643711; DOI: 10.1016/j.scr.2024.103420 CTUi001-A 2024-06-00 2024-06-00 PubMed: 38643711 DOI: 10.1016/j.scr.2024.103420Associated cell lines:
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Chen G, Bai R, Huang P, Liu X, Ni J, Chen L
Generation of a homozygous DNAJC19 knockout human embryonic stem cell line by CRISPR/Cas9 system
Chen G et al. Generation of a homozygous DNAJC19 knockout human embryonic stem cell line by CRISPR/Cas9 system. . 2024-06-00. Pubmed ID: 38696852; DOI: 10.1016/j.scr.2024.103427 WAe007-A-3 2024-06-00 2024-06-00 PubMed: 38696852 DOI: 10.1016/j.scr.2024.103427Associated cell lines:
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Song M, Chen S, Zhang M, Hu S, Lei W, Yu M
Generation of a human induced pluripotent stem cell line harboring heteroplasmic m.3243A > G mutation in MT-TL1 gene
Song M et al. Generation of a human induced pluripotent stem cell line harboring heteroplasmic m.3243A > G mutation in MT-TL1 gene. . 2024-06-00. Pubmed ID: 38489977; DOI: 10.1016/j.scr.2024.103387 ICSSUi005-A 2024-06-00 2024-06-00 PubMed: 38489977 DOI: 10.1016/j.scr.2024.103387Associated cell lines:
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Liu HB, Dong T, Deng L, Zhou C, Tang F, Margolis RL, Li PP
Generation of a human induced pluripotent stem cell line JHUi004-A with heterozygous mutation for spinocerebellar ataxia type 12 using genome editing
Liu HB et al. Generation of a human induced pluripotent stem cell line JHUi004-A with heterozygous mutation for spinocerebellar ataxia type 12 using genome editing. . 2024-06-00. Pubmed ID: 38759410; DOI: 10.1016/j.scr.2024.103441; PMC: PMC11610223 JHUi004-A 2024-06-00 2024-06-00 PubMed: 38759410 DOI: 10.1016/j.scr.2024.103441Associated cell lines:
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Bai X, Chen J, Zhao X, Zhu X, Ding X, Zhang T, Jiang M, Sun X
Generation of an induced pluripotent stem cell line (SJTUGHi001-A) from a patient with Retinitis Pigmentosa carrying c.77C > T mutation in RAX2 gene
Bai X et al. Generation of an induced pluripotent stem cell line (SJTUGHi001-A) from a patient with Retinitis Pigmentosa carrying c.77C > T mutation in RAX2 gene. . 2024-06-00. Pubmed ID: 38507880; DOI: 10.1016/j.scr.2024.103390 SJTUGHi001-A 2024-06-00 2024-06-00 PubMed: 38507880 DOI: 10.1016/j.scr.2024.103390Associated cell lines:
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Gao Xuesong
Language education in a brave new world: A dialectical imagination
Gao Xuesong. Language education in a brave new world: A dialectical imagination. . 2024-06-00. DOI: 10.1111/modl.12930 ZJSHDPi001-A 2024-06-00 2024-06-00 DOI: 10.1111/modl.12930Associated cell lines:
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Li B, Ye X, Lin J, Ma K, He M, Fang Y
Generation of a human induced pluripotent stem cell line (SHUPLi002-A) from PBMCs of a healthy female donor
Li B et al. Generation of a human induced pluripotent stem cell line (SHUPLi002-A) from PBMCs of a healthy female donor. . 2024-06-00. Pubmed ID: 38631181; DOI: 10.1016/j.scr.2024.103422 SHUPLi002-A 2024-06-00 2024-06-00 PubMed: 38631181 DOI: 10.1016/j.scr.2024.103422Associated cell lines:
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Wang P, Sun W, Gong J, Han X, Xu C, Chen Y, Yang Y, Luan H, Li S, Li R, Wen B, Lv S, Chen R, Guo J, Wei C
Generation of human induced pluripotent stem cell line (XWHNi004-A) from a male with APOE gene mutation
Wang P et al. Generation of human induced pluripotent stem cell line (XWHNi004-A) from a male with APOE gene mutation. . 2024-06-00. Pubmed ID: 38552354; DOI: 10.1016/j.scr.2024.103398 XWHNi001-AXWHNi004-A 2024-06-00 2024-06-00 PubMed: 38552354 DOI: 10.1016/j.scr.2024.103398Associated cell lines:
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Maurer W, Rebs S, Köhne S, Eberl H, Wollnik B, Zibat A, Streckfuss-Bömeke K
Generation of a pluripotent stem cell line (UMGi270-A) and a corresponding CRISPR/Cas9 modified isogenic control (UMGi270-A-1) from a patient with sudden onset dilated cardiomyopathy harboring a FLNC p.R2187P mutation
Maurer W et al. Generation of a pluripotent stem cell line (UMGi270-A) and a corresponding CRISPR/Cas9 modified isogenic control (UMGi270-A-1) from a patient with sudden onset dilated cardiomyopathy harboring a FLNC p.R2187P mutation. . 2024-06-00. Pubmed ID: 38583294; DOI: 10.1016/j.scr.2024.103409 UMGi270-AUMGi270-A-1 2024-06-00 2024-06-00 PubMed: 38583294 DOI: 10.1016/j.scr.2024.103409Associated cell lines:
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Veleva D, Ay M, Ovchinnikov DA, Prowse ABJ, Menezes MJ, Nafisinia M
Generation of fibroblast-derived induced pluripotent stem cell (iPSC) lines from two paediatric patients with phenylketonuria
Veleva D et al. Generation of fibroblast-derived induced pluripotent stem cell (iPSC) lines from two paediatric patients with phenylketonuria. . 2024-06-00. Pubmed ID: 38555716; DOI: 10.1016/j.scr.2024.103405 WIMRi003-AWIMRi004-A 2024-06-00 2024-06-00 PubMed: 38555716 DOI: 10.1016/j.scr.2024.103405Associated cell lines:
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Jiang X, Fu C, Liu Q, Gao J
Generation of a KCNQ1 (c.1032 + 2 T > C) mutant human embryonic stem cell line via CRISPR base editing
Jiang X et al. Generation of a KCNQ1 (c.1032 + 2 T > C) mutant human embryonic stem cell line via CRISPR base editing. . 2024-06-00. Pubmed ID: 38653148; DOI: 10.1016/j.scr.2024.103425 WAe009-AWAe009-A-1D 2024-06-00 2024-06-00 PubMed: 38653148 DOI: 10.1016/j.scr.2024.103425Associated cell lines:
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Zhu X, Tang L, Zhang T, Bai X, Chen J, Zhang L, Gong Y, Jiang M, Sun X
Generation of an induced pluripotent stem cell line (SJTUGHi003-A) from a patient with Sorsby fundus dystrophy carrying c.484G>A mutation in TIMP3 gene
Zhu X et al. Generation of an induced pluripotent stem cell line (SJTUGHi003-A) from a patient with Sorsby fundus dystrophy carrying c.484G>A mutation in TIMP3 gene. . 2024-06-00. Pubmed ID: 38640637; DOI: 10.1016/j.scr.2024.103423 SJTUGHi003-A 2024-06-00 2024-06-00 PubMed: 38640637 DOI: 10.1016/j.scr.2024.103423Associated cell lines:
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De Serres-Bérard T, Jauvin D, Pouliot V, Puymirat J, Chahine M
Generation of a lymphoblastoid-derived induced pluripotent stem cell line (CBRCULi015-A) from a patient with congenital myotonic dystrophy
De Serres-Bérard T et al. Generation of a lymphoblastoid-derived induced pluripotent stem cell line (CBRCULi015-A) from a patient with congenital myotonic dystrophy. . 2024-06-00. Pubmed ID: 38704930; DOI: 10.1016/j.scr.2024.103430 CBRCULi001-ACBRCULi002-ACBRCULi003-ACBRCULi004-ACBRCULi005-ACBRCULi010-ACBRCULi011-ACBRCULi012-ACBRCULi013-ACBRCULi015-A 2024-06-00 2024-06-00 PubMed: 38704930 DOI: 10.1016/j.scr.2024.103430Associated cell lines:
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Shao J, Jin Y, Shao C, Zhang X, Yang G
An achievement has been made in establishing an induced pluripotent stem cell line (SDPHi005-A) from a healthy Chinese male donor
Shao J et al. An achievement has been made in establishing an induced pluripotent stem cell line (SDPHi005-A) from a healthy Chinese male donor. . 2024-06-00. Pubmed ID: 38531229; DOI: 10.1016/j.scr.2024.103393 SDQLCHi025-ASDCHi001-ASDPHi005-A 2024-06-00 2024-06-00 PubMed: 38531229 DOI: 10.1016/j.scr.2024.103393Associated cell lines:
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Ahmed E, Fieldès M, Bourguignon C, Mianné J, Petit A, Amel N, Foisset F, Bourdais C, Vachier I, Assou S, De Vos J, Bourdin A
Generation of a healthy heavy smoker patient-derived induced pluripotent stem cell line UHOMi007-A from peripheral blood mononuclear cells
Ahmed E et al. Generation of a healthy heavy smoker patient-derived induced pluripotent stem cell line UHOMi007-A from peripheral blood mononuclear cells. . 2024-06-00. Pubmed ID: 38723411; DOI: 10.1016/j.scr.2024.103437 UHOMi002-AUHOMi007-A 2024-06-00 2024-06-00 PubMed: 38723411 DOI: 10.1016/j.scr.2024.103437Associated cell lines:
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Zhang S, Fan J, Sun H, Hao X, He Y
Generation of a TSC2 knockout embryonic stem cell line by CRISPR/Cas9 editing
Zhang S et al. Generation of a TSC2 knockout embryonic stem cell line by CRISPR/Cas9 editing. . 2024-06-00. Pubmed ID: 38574666; DOI: 10.1016/j.scr.2024.103399 WAe009-A-1F 2024-06-00 2024-06-00 PubMed: 38574666 DOI: 10.1016/j.scr.2024.103399Associated cell lines:
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Han HJ, Kim JH
KSCBi005-A-10(hiPSC-HIF1αKO), a HIF1α knockout human induced pluripotent stem cell line, for demonstrating the role of cellular response to hypoxia
Han HJ et al. KSCBi005-A-10(hiPSC-HIF1αKO), a HIF1α knockout human induced pluripotent stem cell line, for demonstrating the role of cellular response to hypoxia. . 2024-06-00. Pubmed ID: 38636267; DOI: 10.1016/j.scr.2024.103415 KSCBi005-AKSCBi005-A-10 2024-06-00 2024-06-00 PubMed: 38636267 DOI: 10.1016/j.scr.2024.103415Associated cell lines:
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Wu F, Ji X, Gao Y, Liu W, Lu Y, Yang A, Wang J, Chen Q, Zhang X
Generation of a human iPSC line CIPi004-A from a patient with neurofibromatosis type 1 and epilepsy harboring a heterozygous mutation in NF1 gene
Wu F et al. Generation of a human iPSC line CIPi004-A from a patient with neurofibromatosis type 1 and epilepsy harboring a heterozygous mutation in NF1 gene. . 2024-06-00. Pubmed ID: 38761686; DOI: 10.1016/j.scr.2024.103444 CIPi004-A 2024-06-00 2024-06-00 PubMed: 38761686 DOI: 10.1016/j.scr.2024.103444Associated cell lines:
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Ma R, Bi H, Wang Y, Wang J, Zhang J, Yu X, Chen Z, Wang J, Lu C, Zheng J, Li Y, Ding X
Low concentrations of saracatinib promote definitive endoderm differentiation through inhibition of FAK-YAP signaling axis
Ma R et al. Low concentrations of saracatinib promote definitive endoderm differentiation through inhibition of FAK-YAP signaling axis. . 2024-05-30. Pubmed ID: 38816763; DOI: 10.1186/s12964-024-01679-7; PMC: PMC11140888 HECi001-A 2024-05-30 2024-05-30 PubMed: 38816763 DOI: 10.1186/s12964-024-01679-7Associated cell lines:
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Na Hyeon-Jin, Kwon Jae-Eun, Kim Seung-Hyun, Ahn Jiwon, Kwon Ok-Seon, Chung Kyung-Sook
Human Pluripotent Stem Cell-Derived Retinal Organoids: A Viable Platform for Investigating the Efficacy of Adeno-Associated Virus Gene Therapy
Na Hyeon-Jin et al. Human Pluripotent Stem Cell-Derived Retinal Organoids: A Viable Platform for Investigating the Efficacy of Adeno-Associated Virus Gene Therapy. . 2024-05-30. DOI: 10.15283/ijsc23071 KRIBBi006-A 2024-05-30 2024-05-30 DOI: 10.15283/ijsc23071Associated cell lines:
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Şen B.
Autoinflammatory diseases
Şen B.. Autoinflammatory diseases. . 2024-05-28. DOI: 10.1201/9781003124351-20 NIHTVBi016-ANIHTVBi017-ANIHTVBi018-A 2024-05-28 2024-05-28 DOI: 10.1201/9781003124351-20Associated cell lines:
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Zhou X, Zhao L, Wang C, Sun W, Jia B, Li D, Fu J
Diverse functions and pathogenetic role of Crumbs in retinopathy
Zhou X et al. Diverse functions and pathogenetic role of Crumbs in retinopathy. . 2024-05-27. Pubmed ID: 38802833; DOI: 10.1186/s12964-024-01673-z; PMC: PMC11129452 LEIi006-ALEIi016-ALEIi016-B 2024-05-27 2024-05-27 PubMed: 38802833 DOI: 10.1186/s12964-024-01673-z -
Jiang YZ, Hu LY, Chen MS, Wang XJ, Tan CN, Xue PP, Yu T, He XY, Xiang LX, Xiao YN, Li XL, Ran Q, Li ZJ, Chen L
GATA binding protein 2 mediated ankyrin repeat domain containing 26 high expression in myeloid-derived cell lines
Jiang YZ et al. GATA binding protein 2 mediated ankyrin repeat domain containing 26 high expression in myeloid-derived cell lines. . 2024-05-26. Pubmed ID: 38817334; DOI: 10.4252/wjsc.v16.i5.538; PMC: PMC11135246 SHAMUi001-A 2024-05-26 2024-05-26 PubMed: 38817334 DOI: 10.4252/wjsc.v16.i5.538Associated cell lines:
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Barolo L, Gigante Y, Mautone L, Ghirga S, Soloperto A, Giorgi A, Ghirga F, Pitea M, Incocciati A, Mura F, Ruocco G, Boffi A, Baiocco P, Di Angelantonio S
Ferritin nanocage-enabled detection of pathological tau in living human retinal cells
Barolo L et al. Ferritin nanocage-enabled detection of pathological tau in living human retinal cells. . 2024-05-21. Pubmed ID: 38773170; DOI: 10.1038/s41598-024-62188-8; PMC: PMC11109090 SIGi001-ASIGi001-A-13 2024-05-21 2024-05-21 PubMed: 38773170 DOI: 10.1038/s41598-024-62188-8Associated cell lines:
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Schröter Julian, Deininger Luca, Lupse Blaz, Richter Petra, Syrbe Steffen, Mikut Ralf, Jung-Klawitter Sabine
A large and diverse brain organoid dataset of 1,400 cross-laboratory images of 64 trackable brain organoids
Schröter Julian et al. A large and diverse brain organoid dataset of 1,400 cross-laboratory images of 64 trackable brain organoids. . 2024-05-20. DOI: 10.1038/s41597-024-03330-z DHMCi008-ADHMCi009-A 2024-05-20 2024-05-20 DOI: 10.1038/s41597-024-03330-zAssociated cell lines:
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Öttl M, Toonen RF, Verhage M
Reduced synaptic depression in human neurons carrying homozygous disease-causing STXBP1 variant L446F
Öttl M et al. Reduced synaptic depression in human neurons carrying homozygous disease-causing STXBP1 variant L446F. . 2024-05-18. Pubmed ID: 38484778; DOI: 10.1093/hmg/ddae035; PMC: PMC11102591 BIONi010-CBIONi010-C-13 2024-05-18 2024-05-18 PubMed: 38484778 DOI: 10.1093/hmg/ddae035Associated cell lines:
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Tripathi Utkarsh, Rosh Idan, Ben Ezer Ran, Nayak Ritu, Hussein Yara, Choudhary Ashwani, Djamus Jose, Manole Andreea, Houlden Henry, Gage Fred H., Stern Shani
Upregulated ECM genes and increased synaptic activity in Parkinson’s human DA neurons with PINK1/ PRKN mutations
Tripathi Utkarsh et al. Upregulated ECM genes and increased synaptic activity in Parkinson’s human DA neurons with PINK1/ PRKN mutations. . 2024-05-18. DOI: 10.1038/s41531-024-00715-0 UOHi002-AUOHi003-A 2024-05-18 2024-05-18 DOI: 10.1038/s41531-024-00715-0 -
Kumar M, Sahni S, A V, Kumar D, Kushwah N, Goel D, Kapoor H, Srivastava AK, Faruq M
Molecular clues unveiling spinocerebellar ataxia type-12 pathogenesis
Kumar M et al. Molecular clues unveiling spinocerebellar ataxia type-12 pathogenesis. . 2024-05-17. Pubmed ID: 38711441; DOI: 10.1016/j.isci.2024.109768; PMC: PMC11070597 ADBSi001-AIGIBi002-AIGIBi003-AIGIBi004-A 2024-05-17 2024-05-17 PubMed: 38711441 DOI: 10.1016/j.isci.2024.109768Associated cell lines:
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Allison Reilly L., Welby Emily, Ehlers Vanessa, Burand Anthony, Isaeva Olena, Nieves Torres Damaris, Highland Janelle, Brandow Amanda M., Stucky Cheryl L., Ebert Allison D.
Sickle cell disease iPSC-derived sensory neurons exhibit increased excitability and sensitization to patient plasma
Allison Reilly L. et al. Sickle cell disease iPSC-derived sensory neurons exhibit increased excitability and sensitization to patient plasma. . 2024-05-16. DOI: 10.1182/blood.2023022591 IGIBi001-A 2024-05-16 2024-05-16 DOI: 10.1182/blood.2023022591Associated cell lines:
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Beckenkamp LR, da Silva CG, Von Hohendorff MLI, Ogliari KS
Manufacturing Parameters for the Creation of Clinical-Grade Human-Induced Pluripotent Stem Cell Lines From Umbilical Cord Mesenchymal Stromal Cells
Beckenkamp LR et al. Manufacturing Parameters for the Creation of Clinical-Grade Human-Induced Pluripotent Stem Cell Lines From Umbilical Cord Mesenchymal Stromal Cells. . 2024-05-14. Pubmed ID: 38402590; DOI: 10.1093/stcltm/szae010; PMC: PMC11092272 HCORDi001-AHCORDi001-BHCORDi001-CHCORDi001-DHCORDi001-EHCORDi001-FHCORDi001-GHCORDi001-HHCORDi001-IHCORDi001-J 2024-05-14 2024-05-14 PubMed: 38402590 DOI: 10.1093/stcltm/szae010Associated cell lines:
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Yin X, Li Q, Shu Y, Wang H, Thomas B, Maxwell JT, Zhang Y
Exploiting urine-derived induced pluripotent stem cells for advancing precision medicine in cell therapy, disease modeling, and drug testing
Yin X et al. Exploiting urine-derived induced pluripotent stem cells for advancing precision medicine in cell therapy, disease modeling, and drug testing. . 2024-05-09. Pubmed ID: 38724973; DOI: 10.1186/s12929-024-01035-4; PMC: PMC11084032 ZZUi004-AXDCMHi001-ACSUASOi001-ASDQLCHi008-ACPGHi001-ACSUASOi006-AHNMUi002-AHNMUi003-AHNMUi004-AHNMUi005-AHNMUi006-AHNMUi007-AHNMUi008-AHNMUi009-AHNMUi010-AWMUi017-ASXMUi001-AKEIOi005-ASMBCi019-A 2024-05-09 2024-05-09 PubMed: 38724973 DOI: 10.1186/s12929-024-01035-4 -
Wu Lei, Lu Jing, Lan Tianye, Zhang Dongmei, Xu Hanying, Kang Zezheng, Peng Fang, Wang Jian
Stem cell therapies: a new era in the treatment of multiple sclerosis
Wu Lei et al. Stem cell therapies: a new era in the treatment of multiple sclerosis. . 2024-05-09. DOI: 10.3389/fneur.2024.1389697 ZZUi011-A 2024-05-09 2024-05-09 DOI: 10.3389/fneur.2024.1389697Associated cell lines:
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Nazari Mostafa, De Costa Peter I.
EMI teachers’ emotion labour: capturing classroom, institutional and sociocultural ecologies
Nazari Mostafa et al. EMI teachers’ emotion labour: capturing classroom, institutional and sociocultural ecologies. . 2024-05-08. DOI: 10.1080/01434632.2024.2348600 ZJSHDPi001-A 2024-05-08 2024-05-08 DOI: 10.1080/01434632.2024.2348600Associated cell lines:
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Sornjai Wannapa, Promma Ploenphit, Priewkhiew Suphansa, Ramphan Suwipa, Jaratsittisin Janejira, Jinagool Pailin, Wikan Nitwara, Greenwood Michael, Murphy David, Smith Duncan R.
The interaction of GRP78 and Zika virus E and NS1 proteins occurs in a chaperone-client manner
Sornjai Wannapa et al. The interaction of GRP78 and Zika virus E and NS1 proteins occurs in a chaperone-client manner. . 2024-05-06. DOI: 10.1038/s41598-024-61195-z MUSIi011-AMUSIi011-B 2024-05-06 2024-05-06 DOI: 10.1038/s41598-024-61195-zAssociated cell lines:
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Cosker Katharina, Boorman Emily, Vasilopoulou Foteini, Mallach Anna, Piers Thomas M, Pocock Jennifer M
Fibrinogen signalling in human iPSC-derived microglia
Cosker Katharina et al. Fibrinogen signalling in human iPSC-derived microglia. . 2024-05-06. DOI: 10.21203/rs.3.rs-4324378/v1 BIONi010-C 2024-05-06 2024-05-06 DOI: 10.21203/rs.3.rs-4324378/v1Associated cell lines:
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Zibold Julia, Lessard Lola E R, Picard Flavien, da Silva Lara Gruijs, Zadorozhna Yelyzaveta, Streichenberger Nathalie, Belotti Edwige, Osseni Alexis, Emerit Andréa, Errazuriz-Cerda Elisabeth, Michel-Calemard Laurence, Menassa Rita, Coudert Laurent, Wiessner Manuela, Stucka Rolf, Klopstock Thomas, Simonetti Francesca, Hutten Saskia, Nonaka Takashi, Hasegawa Masato, Strom Tim M, Bernard Emilien, Ollagnon Elisabeth, Urtizberea Andoni, Dormann Dorothee, Petiot Philippe, Schaeffer Laurent, Senderek Jan, Leblanc Pascal
The new missense G376V-TDP-43 variant induces late-onset distal myopathy but not amyotrophic lateral sclerosis
Zibold Julia et al. The new missense G376V-TDP-43 variant induces late-onset distal myopathy but not amyotrophic lateral sclerosis. . 2024-05-03. DOI: 10.1093/brain/awad410 CSSi013-A 2024-05-03 2024-05-03 DOI: 10.1093/brain/awad410Associated cell lines:
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De Sousa Paul A., Perfect Leo, Ye Jinpei, Samuels Kay, Piotrowska Ewa, Gordon Martin, Mate Ryan, Abranches Elsa, Wishart Thomas M., Dockrell David H., Courtney Aidan
Hyaluronan in mesenchymal stromal cell lineage differentiation from human pluripotent stem cells: application in serum free culture
De Sousa Paul A. et al. Hyaluronan in mesenchymal stromal cell lineage differentiation from human pluripotent stem cells: application in serum free culture. . 2024-05-03. DOI: 10.1186/s13287-024-03719-y RCe013-A 2024-05-03 2024-05-03 DOI: 10.1186/s13287-024-03719-yAssociated cell lines:
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Liu Zhichen, Qin Qing, Zhang Chongyan, Xu Xiaolong, Dai Dongliang, Lan Mingxi, Wang Yichuan, Zhang Jingwen, Zhao Dan, Kong Deqing, Qin Tian, Wu Danni, Gong Xuedan, Zhou Xingyu, Suhe Alatan, Wang Zhixin, Liu Zhihong
Effects of nonsynonymous single nucleotide polymorphisms of the KIAA1217, SNTA1 and LTBP1 genes on the growth traits of Ujumqin sheep
Liu Zhichen et al. Effects of nonsynonymous single nucleotide polymorphisms of the KIAA1217, SNTA1 and LTBP1 genes on the growth traits of Ujumqin sheep. . 2024-05-02. DOI: 10.3389/fvets.2024.1382897 WAe009-AWAe009-A-50 2024-05-02 2024-05-02 DOI: 10.3389/fvets.2024.1382897Associated cell lines:
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Yang Xiaoping, Delsante Marco, Daneshpajouhnejad Parnaz, Fenaroli Paride, Mandell Kira Perzel, Wang Xiaoxin, Takahashi Shogo, Halushka Marc K., Kopp Jeffrey B., Levi Moshe, Rosenberg Avi Z.
Bile Acid Receptor Agonist Reverses Transforming Growth Factor-β1–Mediated Fibrogenesis in Human Induced Pluripotent Stem Cells–Derived Kidney Organoids
Yang Xiaoping et al. Bile Acid Receptor Agonist Reverses Transforming Growth Factor-β1–Mediated Fibrogenesis in Human Induced Pluripotent Stem Cells–Derived Kidney Organoids. . 2024-05-00. DOI: 10.1016/j.labinv.2024.100336 MUi027-A 2024-05-00 2024-05-00 DOI: 10.1016/j.labinv.2024.100336Associated cell lines:
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Alizadeh Farzaneh, Abraghan Yousef Jafari, Farrokhi Shima, Yousefi Yasamin, Mirahmadi Yeganeh, Eslahi Atieh, Mojarrad Majid
Production of Duchenne muscular dystrophy cellular model using CRISPR-Cas9 exon deletion strategy
Alizadeh Farzaneh et al. Production of Duchenne muscular dystrophy cellular model using CRISPR-Cas9 exon deletion strategy. . 2024-05-00. DOI: 10.1007/s11010-023-04759-3 MUNIi001-AMUNIi003-A 2024-05-00 2024-05-00 DOI: 10.1007/s11010-023-04759-3Associated cell lines:
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Kurzawa-Akanbi Marzena, Tzoumas Nikolaos, Corral-Serrano Julio C., Guarascio Rosellina, Steel David H., Cheetham Michael E., Armstrong Lyle, Lako Majlinda
Pluripotent stem cell-derived models of retinal disease: Elucidating pathogenesis, evaluating novel treatments, and estimating toxicity
Kurzawa-Akanbi Marzena et al. Pluripotent stem cell-derived models of retinal disease: Elucidating pathogenesis, evaluating novel treatments, and estimating toxicity. . 2024-05-00. DOI: 10.1016/j.preteyeres.2024.101248 SCTCi014-ASCTCi014-A-1 2024-05-00 2024-05-00 DOI: 10.1016/j.preteyeres.2024.101248Associated cell lines:
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Chen D, Su J, Huang X, Chen H, Jiang T, Zhi C, Zhou Z, Zhang B, Yu L, Jiang X
Establishment and characterization of ZJUCHi003: an induced pluripotent stem cell line from a patient with Temple-Baraitser/Zimmermann-Laband syndrome carrying KCNH1 c.1070G > A (p.R357Q) variant
Chen D et al. Establishment and characterization of ZJUCHi003: an induced pluripotent stem cell line from a patient with Temple-Baraitser/Zimmermann-Laband syndrome carrying KCNH1 c.1070G > A (p.R357Q) variant. . 2024-05-00. Pubmed ID: 38372889; DOI: 10.1007/s13577-024-01031-8 ZJUCHi003-A 2024-05-00 2024-05-00 PubMed: 38372889 DOI: 10.1007/s13577-024-01031-8Associated cell lines:
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Salerno José Alexandre, Rehen Stevens
Human pluripotent stem cells as a translational toolkit in psychedelic research in vitro
Salerno José Alexandre et al. Human pluripotent stem cells as a translational toolkit in psychedelic research in vitro. . 2024-05-00. DOI: 10.1016/j.isci.2024.109631 GIBHi002-AUNIBSi012-AUNIBSi013-AGIBHi002-A-5 2024-05-00 2024-05-00 DOI: 10.1016/j.isci.2024.109631Associated cell lines:
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Zhang Xiaolong, Shi Tao, Li Jin, Wu Xiaonan, Wu Kaili, Li Danyang, Wang Dayong, Guan Jing, Wang Hongyang
Natural History of KCNQ4
Zhang Xiaolong et al. Natural History of KCNQ4p.G285S Related Hearing Loss, Construction ofiPSC and Mouse Modelp.G285S Related Hearing Loss, Construction ofiPSC and Mouse Model. . 2024-05-00. DOI: 10.1002/lary.31179 CPGHi001-ACPGHi003-ACPGHi001-A-1 2024-05-00 2024-05-00 DOI: 10.1002/lary.31179Associated cell lines:
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De Mori Roberta, Tardivo Silvia, Pollara Lidia, Giliani Silvia Clara, Ali Eltahir, Giordano Lucio, Leuzzi Vincenzo, Fischetto Rita, Gener Blanca, Diprima Santo, Morelli Marco J., Monti Maria Cristina, Sottile Virginie, Valente Enza Maria
Joubert syndrome-derived induced pluripotent stem cells show altered neuronal differentiation in vitro
De Mori Roberta et al. Joubert syndrome-derived induced pluripotent stem cells show altered neuronal differentiation in vitro. . 2024-05-00. DOI: 10.1007/s00441-024-03876-9 CSSi001-ACSSi007-A 2024-05-00 2024-05-00 DOI: 10.1007/s00441-024-03876-9 -
Aizenshtadt A, Wang C, Abadpour S, Menezes PD, Wilhelmsen I, Dalmao-Fernandez A, Stokowiec J, Golovin A, Johnsen M, Combriat TMD, Røberg-Larsen H, Gadegaard N, Scholz H, Busek M, Krauss SJK
Pump-Less, Recirculating Organ-on-Chip (rOoC) Platform to Model the Metabolic Crosstalk between Islets and Liver
Aizenshtadt A et al. Pump-Less, Recirculating Organ-on-Chip (rOoC) Platform to Model the Metabolic Crosstalk between Islets and Liver. . 2024-05-00. Pubmed ID: 38221504; DOI: 10.1002/adhm.202303785; PMC: PMC11468483 WTSIi013-A 2024-05-00 2024-05-00 PubMed: 38221504 DOI: 10.1002/adhm.202303785Associated cell lines:
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Frenz-Wiessner S, Fairley SD, Buser M, Goek I, Salewskij K, Jonsson G, Illig D, Zu Putlitz B, Petersheim D, Li Y, Chen PH, Kalauz M, Conca R, Sterr M, Geuder J, Mizoguchi Y, Megens RTA, Linder MI, Kotlarz D, Rudelius M, Penninger JM, Marr C, Klein C
Generation of complex bone marrow organoids from human induced pluripotent stem cells
Frenz-Wiessner S et al. Generation of complex bone marrow organoids from human induced pluripotent stem cells. . 2024-05-00. Pubmed ID: 38374263; DOI: 10.1038/s41592-024-02172-2; PMC: PMC11093744 SCTi003-A 2024-05-00 2024-05-00 PubMed: 38374263 DOI: 10.1038/s41592-024-02172-2Associated cell lines:
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Silber Sherman J., Goldsmith Sierra, Castleman Leilani, Hayashi Katsuhiko
In Vitro Maturation, In Vitro Oogenesis, and Ovarian Longevity
Silber Sherman J. et al. In Vitro Maturation, In Vitro Oogenesis, and Ovarian Longevity. . 2024-05-00. DOI: 10.1007/s43032-023-01427-1 UCLAi004-AUCLAi004-BUCLAi004-CUCLAi005-AUCLAi005-BUCLAi005-C 2024-05-00 2024-05-00 DOI: 10.1007/s43032-023-01427-1Associated cell lines:
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Josvai Mitchell, Polyak Erzsebet, Kalluri Meghana, Robertson Samantha, Crone Wendy C., Suzuki Masatoshi
An engineered in vitro model of the human myotendinous junction
Josvai Mitchell et al. An engineered in vitro model of the human myotendinous junction. . 2024-05-00. DOI: 10.1016/j.actbio.2024.04.007 ICGi002-AICGi002-BICGi002-CIGIBi006-AIGIBi008-A 2024-05-00 2024-05-00 DOI: 10.1016/j.actbio.2024.04.007Associated cell lines:
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Bogomiakova Margarita E., Bogomazova Alexandra N., Lagarkova Maria A.
Dysregulation of Immune Tolerance to Autologous iPSCs and Their Differentiated Derivatives
Bogomiakova Margarita E. et al. Dysregulation of Immune Tolerance to Autologous iPSCs and Their Differentiated Derivatives. . 2024-05-00. DOI: 10.1134/s0006297924050031 RCPCMi007-ARCPCMi007-A-1 2024-05-00 2024-05-00 DOI: 10.1134/s0006297924050031Associated cell lines:
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Shinsato Rogério N., Correa Camila Graczyk, Herai Roberto H.
Genetic network analysis indicate that individuals affected by neurodevelopmental conditions have genetic variations associated with ophthalmologic alterations: A critical review of literature
Shinsato Rogério N. et al. Genetic network analysis indicate that individuals affected by neurodevelopmental conditions have genetic variations associated with ophthalmologic alterations: A critical review of literature. . 2024-05-00. DOI: 10.1016/j.gene.2024.148246 SBWCHi001-A 2024-05-00 2024-05-00 DOI: 10.1016/j.gene.2024.148246Associated cell lines:
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Mancuso R, Fattorelli N, Martinez-Muriana A, Davis E, Wolfs L, Van Den Daele J, Geric I, Premereur J, Polanco P, Bijnens B, Preman P, Serneels L, Poovathingal S, Balusu S, Verfaillie C, Fiers M, De Strooper B
Xenografted human microglia display diverse transcriptomic states in response to Alzheimer's disease-related amyloid-β pathology
Mancuso R et al. Xenografted human microglia display diverse transcriptomic states in response to Alzheimer's disease-related amyloid-β pathology. . 2024-05-00. Pubmed ID: 38539015; DOI: 10.1038/s41593-024-01600-y; PMC: PMC11089003 BIONi010-CBIONi010-C-2BIONi010-C-3BIONi010-C-4BIONi010-C-6UKBi011-AUKBi011-A-1UKBi011-A-2UKBi011-A-3 2024-05-00 2024-05-00 PubMed: 38539015 DOI: 10.1038/s41593-024-01600-yAssociated cell lines:
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Kaminska P, Ovesen PL, Jakiel M, Obrebski T, Schmidt V, Draminski M, Bilska AG, Bieniek M, Anink J, Paterczyk B, Jensen AMG, Piatek S, Andersen OM, Aronica E, Willnow TE, Kaminska B, Dabrowski MJ, Malik AR
SorLA restricts TNFα release from microglia to shape a glioma-supportive brain microenvironment
Kaminska P et al. SorLA restricts TNFα release from microglia to shape a glioma-supportive brain microenvironment. . 2024-05-00. Pubmed ID: 38499808; DOI: 10.1038/s44319-024-00117-6; PMC: PMC11094098 HMGUi001-A 2024-05-00 2024-05-00 PubMed: 38499808 DOI: 10.1038/s44319-024-00117-6Associated cell lines:
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Didiasova Miroslava, Banning Antje, Tikkanen Ritva
Development of precision therapies for rare inborn errors of metabolism: Functional investigations in cell culture models
Didiasova Miroslava et al. Development of precision therapies for rare inborn errors of metabolism: Functional investigations in cell culture models. . 2024-05-00. DOI: 10.1002/jimd.12674 DHMCi003-ADHMCi003-B 2024-05-00 2024-05-00 DOI: 10.1002/jimd.12674Associated cell lines:
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Thuma Tobin B.T., Procopio Rebecca A., Jimenez Hiram J., Gunton Kammi B., Pulido Jose S.
Hypomorphic variants in inherited retinal and ocular diseases: A review of the literature with clinical cases
Thuma Tobin B.T. et al. Hypomorphic variants in inherited retinal and ocular diseases: A review of the literature with clinical cases. . 2024-05-00. DOI: 10.1016/j.survophthal.2023.11.006 ESi082-A 2024-05-00 2024-05-00 DOI: 10.1016/j.survophthal.2023.11.006Associated cell lines:
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Wu Jingying, Cheng Xin, Ji Duxin, Niu Huiwen, Yao Songquan, Lv Xukun, Wang Jianqiang, Li Ziyi, Zheng Haoran, Cao Yuwen, Zhan Feixia, Zhang Mengyuan, Tian Wotu, Huang Xiaojun, Luan Xinghua, Cao Li
The Phenotypic and Genotypic Spectrum of
Wu Jingying et al. The Phenotypic and Genotypic Spectrum ofCSF1R ‐Related Disorder in ChinaCSF1R ‐Related Disorder in China. . 2024-05-00. DOI: 10.1002/mds.29764 JTUi007-A 2024-05-00 2024-05-00 DOI: 10.1002/mds.29764Associated cell lines:
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Thöny Beat, Ng Joanne, Kurian Manju A., Mills Philippa, Martinez Aurora
Mouse models for inherited monoamine neurotransmitter disorders
Thöny Beat et al. Mouse models for inherited monoamine neurotransmitter disorders. . 2024-05-00. DOI: 10.1002/jimd.12710 DHMCi003-ADHMCi003-B 2024-05-00 2024-05-00 DOI: 10.1002/jimd.12710Associated cell lines:
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Ging Kathi, Frick Lukas, Schlachetzki Johannes, Armani Andrea, Zhu Yanping, Gilormini Pierre-André, Marques Ana, Dhingra Ashutosh, Böck Desirée, Deen Matthew, Chen Xi, Serdiuk Tetiana, Trevisan Chiara, Sellitto Stefano, Pisano Claudio, Glass Christopher K, Heutink Peter, Yin Jiang-An, Vocadlo David J, Aguzzi Adriano
Direct and indirect regulation of β-glucocerebrosidase by the transcription factorsUSF2andONECUT2
Ging Kathi et al. Direct and indirect regulation of β-glucocerebrosidase by the transcription factorsUSF2andONECUT2. . 2024-04-28. DOI: 10.1101/2024.04.28.591482 UOXFi001-B 2024-04-28 2024-04-28 DOI: 10.1101/2024.04.28.591482Associated cell lines:
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Demchenko Anna, Belova Lyubava, Balyasin Maxim, Kochergin-Nikitsky Konstantin, Kondrateva Ekaterina, Voronina Ekaterina, Pozhitnova Victoria, Tabakov Vyacheslav, Salikhova Diana, Bukharova Tatiana, Goldshtein Dmitry, Kondratyeva Elena, Kyian Tatiana, Amelina Elena, Zubkova Olga, Popova Olga, Ozharovskaia Tatiana, Lavrov Alexander, Smirnikhina Svetlana
Airway basal cells from human-induced pluripotent stem cells: a new frontier in cystic fibrosis research
Demchenko Anna et al. Airway basal cells from human-induced pluripotent stem cells: a new frontier in cystic fibrosis research. . 2024-04-26. DOI: 10.3389/fcell.2024.1336392 RCMGi001-ARCMGi002-ARCMGi004-A 2024-04-26 2024-04-26 DOI: 10.3389/fcell.2024.1336392Associated cell lines:
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Pazzin Douglas, Previato Thales, Budelon Gonçalves João, Zanirati Gabriele, Xavier Fernando, da Costa Jaderson, Marinowic Daniel
Induced Pluripotent Stem Cells and Organoids in Advancing Neuropathology Research and Therapies
Pazzin Douglas et al. Induced Pluripotent Stem Cells and Organoids in Advancing Neuropathology Research and Therapies. . 2024-04-25. DOI: 10.3390/cells13090745 IDISi001-A 2024-04-25 2024-04-25 DOI: 10.3390/cells13090745Associated cell lines:
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Ren Rutong, Jiang Jinhe, Li Xinxin, Zhang Guirong
Research progress of autoimmune diseases based on induced pluripotent stem cells
Ren Rutong et al. Research progress of autoimmune diseases based on induced pluripotent stem cells. . 2024-04-24. DOI: 10.3389/fimmu.2024.1349138 XDCMHi001-ASHFDi001-ASDQLCHi040-ASPHi001-AMETUi001-AMNZTASi001-ADMBi003-ADMBi004-AIBMSi027-ATAUi008-A 2024-04-24 2024-04-24 DOI: 10.3389/fimmu.2024.1349138Associated cell lines:
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Vandermeulen L, Geric I, Fumagalli L, Kreir M, Lu A, Nonneman A, Premereur J, Wolfs L, Policarpo R, Fattorelli N, De Bondt A, Van Den Wyngaert I, Asselbergh B, Fiers M, De Strooper B, d'Ydewalle C, Mancuso R
Regulation of human microglial gene expression and function via RNAase-H active antisense oligonucleotides in vivo in Alzheimer's disease
Vandermeulen L et al. Regulation of human microglial gene expression and function via RNAase-H active antisense oligonucleotides in vivo in Alzheimer's disease. . 2024-04-24. Pubmed ID: 38654375; DOI: 10.1186/s13024-024-00725-9; PMC: PMC11040766 BIONi010-CBIONi010-C-3SIGi001-ABIONi010-C-7UKBi011-AUKBi011-A-1UKBi011-A-3BIONi010-C-17 2024-04-24 2024-04-24 PubMed: 38654375 DOI: 10.1186/s13024-024-00725-9Associated cell lines:
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Danz K, Fleddermann J, Koch M, Fecioru E, Maahs L, Kinsinger N, Krämer J, Kraegeloh A, Wagner S
Evaluation of the Transport and Binding of Dopamine-Loaded PLGA Nanoparticles for the Treatment of Parkinson's Disease Using In Vitro Model Systems
Danz K et al. Evaluation of the Transport and Binding of Dopamine-Loaded PLGA Nanoparticles for the Treatment of Parkinson's Disease Using In Vitro Model Systems. . 2024-04-23. Pubmed ID: 38794233; DOI: 10.3390/pharmaceutics16050571; PMC: PMC11125169 UKKi011-A 2024-04-23 2024-04-23 PubMed: 38794233 DOI: 10.3390/pharmaceutics16050571Associated cell lines:
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Danz K, Fleddermann J, Koch M, Fecioru E, Maahs L, Kinsinger N, Krämer J, Kraegeloh A, Wagner S.
Evaluation of the Transport and Binding of Dopamine-Loaded PLGA Nanoparticles for the Treatment of Parkinson’s Disease Using In Vitro Model Systems
Danz K et al. Evaluation of the Transport and Binding of Dopamine-Loaded PLGA Nanoparticles for the Treatment of Parkinson’s Disease Using In Vitro Model Systems. . 2024-04-23. UKKi011-A 2024-04-23 2024-04-23Associated cell lines:
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Graffunder AS, Bresser AAJ, Fernandez Vallone V, Megges M, Stachelscheid H, Kühnen P, Opitz R
Spatiotemporal expression of thyroid hormone transporter MCT8 and THRA mRNA in human cerebral organoids recapitulating first trimester cortex development
Graffunder AS et al. Spatiotemporal expression of thyroid hormone transporter MCT8 and THRA mRNA in human cerebral organoids recapitulating first trimester cortex development. . 2024-04-23. Pubmed ID: 38654093; DOI: 10.1038/s41598-024-59533-2; PMC: PMC11039642 BIHi005-ABIHi001-BHMGUi001-ABIHi250-A 2024-04-23 2024-04-23 PubMed: 38654093 DOI: 10.1038/s41598-024-59533-2Associated cell lines:
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Pornsukjantra Tanapat, Saikachain Nongluk, Sutjarit Nareerat, Khongkrapan Arthaporn, Tubsuwan Alisa, Bhukhai Kanit, Tim-Aroon Thipwimol, Anurathapan Usanarat, Hongeng Suradej, Asavapanumas Nithi
An increase in ER stress and unfolded protein response in iPSCs-derived neuronal cells from neuronopathic Gaucher disease patients
Pornsukjantra Tanapat et al. An increase in ER stress and unfolded protein response in iPSCs-derived neuronal cells from neuronopathic Gaucher disease patients. . 2024-04-22. DOI: 10.1038/s41598-024-59834-6 MUi030-AMUi031-A 2024-04-22 2024-04-22 DOI: 10.1038/s41598-024-59834-6 -
Petersilie L, Heiduschka S, Nelson JSE, Neu LA, Le S, Anand R, Kafitz KW, Prigione A, Rose CR
Cortical brain organoid slices (cBOS) for the study of human neural cells in minimal networks
Petersilie L et al. Cortical brain organoid slices (cBOS) for the study of human neural cells in minimal networks. . 2024-04-19. Pubmed ID: 38523789; DOI: 10.1016/j.isci.2024.109415; PMC: PMC10957451 HVRDi004-BHMGUi001-AHHUUKDi009-A 2024-04-19 2024-04-19 PubMed: 38523789 DOI: 10.1016/j.isci.2024.109415Associated cell lines:
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Durinova Anna, Smutna Lucie, Barta Pavel, Kamaraj Rajamanikkam, Smutny Tomas, Schmierer Bernhard, Pavek Petr, Trejtnar Frantisek
Radiolabeled 15-mer peptide internalization is mediated by megalin (LRP2 receptor) in a CRISPR/Cas9-based LRP2 knockout human kidney cell model
Durinova Anna et al. Radiolabeled 15-mer peptide internalization is mediated by megalin (LRP2 receptor) in a CRISPR/Cas9-based LRP2 knockout human kidney cell model. . 2024-04-18. DOI: 10.1186/s41181-024-00262-2 WAe009-A-56 2024-04-18 2024-04-18 DOI: 10.1186/s41181-024-00262-2Associated cell lines:
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Chen Yi, Li Meng, Wu Yanqing
The occurrence and development of induced pluripotent stem cells
Chen Yi et al. The occurrence and development of induced pluripotent stem cells. . 2024-04-18. DOI: 10.3389/fgene.2024.1389558 TUSMi001-AZZUi005-AUOWi005-AUHOMi001-AINMi001-AINMi002-AINMi003-AINMi004-AINMi005-A 2024-04-18 2024-04-18 DOI: 10.3389/fgene.2024.1389558Associated cell lines:
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Komatsu Hiroaki, Okawa Masayo, Kazuki Yasuhiro, Kazuki Kanako, Hichiwa Genki, Shimoya Kazuto, Sato Shinya, Taniguchi Fuminori, Oshimura Mitsuo, Harada Tasuku
Characterization of immortalized ovarian epithelial cells with BRCA1/2 mutation
Komatsu Hiroaki et al. Characterization of immortalized ovarian epithelial cells with BRCA1/2 mutation. . 2024-04-14. DOI: 10.1007/s13577-024-01064-z MUSIi007-AVRISGi001-ATAUi008-A 2024-04-14 2024-04-14 DOI: 10.1007/s13577-024-01064-zAssociated cell lines:
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Do QB, Noor H, Marquez-Gomez R, Cramb KML, Ng B, Abbey A, Ibarra-Aizpurua N, Caiazza MC, Sharifi P, Lang C, Beccano-Kelly D, Baleriola J, Bengoa-Vergniory N, Wade-Martins R
Early deficits in an in vitro striatal microcircuit model carrying the Parkinson's GBA-N370S mutation
Do QB et al. Early deficits in an in vitro striatal microcircuit model carrying the Parkinson's GBA-N370S mutation. . 2024-04-12. Pubmed ID: 38609392; DOI: 10.1038/s41531-024-00694-2; PMC: PMC11014935 UOXFi001-BUOXFi003-ASTBCi101-A 2024-04-12 2024-04-12 PubMed: 38609392 DOI: 10.1038/s41531-024-00694-2Associated cell lines:
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Hofmann Lukas, Grüner Julia, Klug Katharina, Breyer Maximilian, Klein Thomas, Hochheimer Vanessa, Wagenhäuser Laura, Wischmeyer Erhard, Üçeyler Nurcan
Elevated interleukin-8 expression by skin fibroblasts as a potential contributor to pain in women with Fabry disease
Hofmann Lukas et al. Elevated interleukin-8 expression by skin fibroblasts as a potential contributor to pain in women with Fabry disease. . 2024-04-09. DOI: 10.1371/journal.pone.0300687 UKWNLi001-A 2024-04-09 2024-04-09 DOI: 10.1371/journal.pone.0300687Associated cell lines:
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Yamada S, Hashita T, Yanagida S, Sato H, Yasuhiko Y, Okabe K, Noda T, Nishida M, Matsunaga T, Kanda Y
SARS-CoV-2 causes dysfunction in human iPSC-derived brain microvascular endothelial cells potentially by modulating the Wnt signaling pathway
Yamada S et al. SARS-CoV-2 causes dysfunction in human iPSC-derived brain microvascular endothelial cells potentially by modulating the Wnt signaling pathway. . 2024-04-08. Pubmed ID: 38584257; DOI: 10.1186/s12987-024-00533-9; PMC: PMC11000354 WISCi004-B 2024-04-08 2024-04-08 PubMed: 38584257 DOI: 10.1186/s12987-024-00533-9Associated cell lines:
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Fazeli Elnaz, Fazeli Elham, Fojtík Petr, Holstege Henne, Andersen Olav M.
Functional characterization of SORL1 variants in cell-based assays to investigate variant pathogenicity
Fazeli Elnaz et al. Functional characterization of SORL1 variants in cell-based assays to investigate variant pathogenicity. . 2024-04-08. DOI: 10.1098/rstb.2022.0377 UMi038-AUMi039-A 2024-04-08 2024-04-08 DOI: 10.1098/rstb.2022.0377 -
Emperador Sonia, Habbane Mouna, López-Gallardo Ester, del Rio Alejandro, Llobet Laura, Mateo Javier, Sanz-López Ana María, Fernández-García María José, Sánchez-Tocino Hortensia, Benbunan-Ferreiro Sol, Calabuig-Goena María, Narvaez-Palazón Carlos, Fernández-Vega Beatriz, González-Iglesias Hector, Urreizti Roser, Artuch Rafael, Pacheu-Grau David, Bayona-Bafaluy Pilar, Montoya Julio, Ruiz-Pesini Eduardo
Identification and characterization of a new pathologic mutation in a large Leber hereditary optic neuropathy pedigree
Emperador Sonia et al. Identification and characterization of a new pathologic mutation in a large Leber hereditary optic neuropathy pedigree. . 2024-04-06. DOI: 10.1186/s13023-024-03165-2 FINCBi001-A 2024-04-06 2024-04-06 DOI: 10.1186/s13023-024-03165-2Associated cell lines:
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Lemarié L, Courtial EJ, Sohier J
Method for Large-scale Production of hIPSC Spheroids
Lemarié L et al. Method for Large-scale Production of hIPSC Spheroids. . 2024-04-05. Pubmed ID: 38618177; DOI: 10.21769/bioprotoc.4965; PMC: PMC11006805 SCTi003-APGNMi001-A 2024-04-05 2024-04-05 PubMed: 38618177 DOI: 10.21769/bioprotoc.4965Associated cell lines:
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Lickert Heiko, Yang Kaiyuan, Spitzer Hannah, Sterr Michael, Hrovatin Karin, O Sean de la, Zhang Xinghao, Setyono Eunike, Ud-Dean Minhaz, Walzthoeni Thomas, Flisikowski Krzysztof, Flisikowska Tatiana, Schnieke Angelika, Scheibner Katharina, Wells James, Sneddon Julie, Kessler Barbara, Wolf Eckhard, Kemter Elisabeth, Theis Fabian
A multimodal cross-species comparison of pancreas development
Lickert Heiko et al. A multimodal cross-species comparison of pancreas development. . 2024-04-04. DOI: 10.21203/rs.3.rs-4151759/v1 HMGUi001-A 2024-04-04 2024-04-04 DOI: 10.21203/rs.3.rs-4151759/v1Associated cell lines:
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Yan Shiju, Song Chengli, Yang Yuqing, Xu Jilei, Chen Yanjie, Zhou Yu
Design and implementation of mechanical property testing equipment for thoracic aortic stent grafts
Yan Shiju et al. Design and implementation of mechanical property testing equipment for thoracic aortic stent grafts. . 2024-04-02. DOI: 10.1080/13645706.2023.2295951 ICSSUi002-A 2024-04-02 2024-04-02 DOI: 10.1080/13645706.2023.2295951Associated cell lines:
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Suárez-Herrera Nuria, Garanto Alejandro, Collin Rob W.J.
Understanding and Rescuing the Splicing Defect Caused by the Frequent ABCA4 Variant c.4253+43G>A Underlying Stargardt Disease
Suárez-Herrera Nuria et al. Understanding and Rescuing the Splicing Defect Caused by the Frequent ABCA4 Variant c.4253+43G>A Underlying Stargardt Disease. . 2024-04-01. DOI: 10.1089/nat.2023.0076 RMCGENi020-A 2024-04-01 2024-04-01 DOI: 10.1089/nat.2023.0076Associated cell lines:
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Mullen M, Kojic A, Alamana C, Canel G, Lai C, Knowles JW, Wu JC
Generation of two induced pluripotent stem cell lines from healthy patients of African American ancestry
Mullen M et al. Generation of two induced pluripotent stem cell lines from healthy patients of African American ancestry. . 2024-04-00. Pubmed ID: 38359472; DOI: 10.1016/j.scr.2024.103322 SCVIi051-ASCVIi053-A 2024-04-00 2024-04-00 PubMed: 38359472 DOI: 10.1016/j.scr.2024.103322Associated cell lines:
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Su S, Zhao F, Zhang H, Liu Y, Li Z, Zhang H, Wang Y, Fang F, Liu Y
Establishment of a transgene-free iPS cell line (SDCHi003-A) from a young patient bearing a NPRL2 mutation and suffering from Epilepsy
Su S et al. Establishment of a transgene-free iPS cell line (SDCHi003-A) from a young patient bearing a NPRL2 mutation and suffering from Epilepsy. . 2024-04-00. Pubmed ID: 38430737; DOI: 10.1016/j.scr.2024.103366 SDCHi003-A 2024-04-00 2024-04-00 PubMed: 38430737 DOI: 10.1016/j.scr.2024.103366Associated cell lines:
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Arunachal G, Milind Nimonkar M, Raghavendra K, Chetan GK, Mehta B, Markandeya YS
Generation of induced pluripotent stem cell line, NIMHi009-A, from PBMCs of an adult healthy male
Arunachal G et al. Generation of induced pluripotent stem cell line, NIMHi009-A, from PBMCs of an adult healthy male. . 2024-04-00. Pubmed ID: 38368738; DOI: 10.1016/j.scr.2024.103349 NIMHi009-A 2024-04-00 2024-04-00 PubMed: 38368738 DOI: 10.1016/j.scr.2024.103349Associated cell lines:
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Dash SS, Arunachal G, Nimonkar MM, Vengalil S, Nashi S, Chetan GK, Boddu VK, Nalini A, Markandeya YS
Generation of induced pluripotent stem cell line NIMHi010-A from dermal fibroblast cells of a healthy individual
Dash SS et al. Generation of induced pluripotent stem cell line NIMHi010-A from dermal fibroblast cells of a healthy individual. . 2024-04-00. Pubmed ID: 38412659; DOI: 10.1016/j.scr.2024.103355 UUMCBi001-AUUMCBi002-ANIMHi010-A 2024-04-00 2024-04-00 PubMed: 38412659 DOI: 10.1016/j.scr.2024.103355Associated cell lines:
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Ratnavadivel S, Dammeier J, Gaertner A, de Toledo MAS, Zenke M, Gummert J, Bloch Rasmussen T, Klinke N, Jürgens K, Meyer H, Paululat A, Milting H
Generation of a TMEM43 knockout human induced pluripotent stem cell line (HDZi003-A-1) using CRISPR/Cas9
Ratnavadivel S et al. Generation of a TMEM43 knockout human induced pluripotent stem cell line (HDZi003-A-1) using CRISPR/Cas9. . 2024-04-00. Pubmed ID: 38430734; DOI: 10.1016/j.scr.2024.103354 HDZi001-AHDZi003-AHDZi003-A-1 2024-04-00 2024-04-00 PubMed: 38430734 DOI: 10.1016/j.scr.2024.103354Associated cell lines:
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Marcó de la Cruz B, Campos J, Molinaro A, Xie X, Jin G, Wei Z, Acuna C, Sterky FH
Liprin-α proteins are master regulators of human presynapse assembly
Marcó de la Cruz B et al. Liprin-α proteins are master regulators of human presynapse assembly. . 2024-04-00. Pubmed ID: 38472649; DOI: 10.1038/s41593-024-01592-9; PMC: PMC11001580 WAe009-A 2024-04-00 2024-04-00 PubMed: 38472649 DOI: 10.1038/s41593-024-01592-9Associated cell lines:
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Xu C, Zhou L, Jiang H, Song T, Liu Z, Duan X, Fang F
Establishment of an iPSC line (BCHNDi001-A) from a patient with nicotinamide nucleotide repair system deficiency caused by biallelic NAXD mutations
Xu C et al. Establishment of an iPSC line (BCHNDi001-A) from a patient with nicotinamide nucleotide repair system deficiency caused by biallelic NAXD mutations. . 2024-04-00. Pubmed ID: 38387170; DOI: 10.1016/j.scr.2024.103346 BCHNDi001-A 2024-04-00 2024-04-00 PubMed: 38387170 DOI: 10.1016/j.scr.2024.103346Associated cell lines:
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Xu W, Chen K, Guo M, Dong Q, Cui M
Establishment of FDHSi003-A, a human induced pluripotent stem cell (hiPSC) line with a mutation of RNF216 c.1948G > T
Xu W et al. Establishment of FDHSi003-A, a human induced pluripotent stem cell (hiPSC) line with a mutation of RNF216 c.1948G > T. . 2024-04-00. Pubmed ID: 38377650; DOI: 10.1016/j.scr.2024.103347 FDHSi003-A 2024-04-00 2024-04-00 PubMed: 38377650 DOI: 10.1016/j.scr.2024.103347Associated cell lines:
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Li Z, Liu C, Xin H, Lv Y, Gao M, Ma J, Liu N, Gai Z, Liu Y
Establishment of a non-integrated iPSC line (SDQLCHi043-A) from a male infant with propionic acidemia carrying compound heterozygote mutations in PCCB gene
Li Z et al. Establishment of a non-integrated iPSC line (SDQLCHi043-A) from a male infant with propionic acidemia carrying compound heterozygote mutations in PCCB gene. . 2024-04-00. Pubmed ID: 38394970; DOI: 10.1016/j.scr.2024.103352 SDQLCHi043-A 2024-04-00 2024-04-00 PubMed: 38394970 DOI: 10.1016/j.scr.2024.103352Associated cell lines:
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Kim MK, Kim Y, Lee N, Moon HJ, Lee JH, Kim EJ, Kim YJ, Kim JH, Jung NY
Generation of an induced pluripotent stem cell line (PNUYHi002-A) from a patient with Alzheimer's disease carrying PRNP M232R variant
Kim MK et al. Generation of an induced pluripotent stem cell line (PNUYHi002-A) from a patient with Alzheimer's disease carrying PRNP M232R variant. . 2024-04-00. Pubmed ID: 38437769; DOI: 10.1016/j.scr.2024.103361 PNUYHi002-A 2024-04-00 2024-04-00 PubMed: 38437769 DOI: 10.1016/j.scr.2024.103361Associated cell lines:
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Zahra S, Kapoor H, Ahmad I, Kamai A, Srivastava AK, Faruq M
Generation of an Induced pluripotent stem cell (iPSC) line (IGIBi011-A) from a Spinocerebellar ataxia type 12 gait dominant patient
Zahra S et al. Generation of an Induced pluripotent stem cell (iPSC) line (IGIBi011-A) from a Spinocerebellar ataxia type 12 gait dominant patient. . 2024-04-00. Pubmed ID: 38340452; DOI: 10.1016/j.scr.2024.103319 IGIBi002-AIGIBi003-AIGIBi004-AIGIBi006-AIGIBi008-AIGIBi011-A 2024-04-00 2024-04-00 PubMed: 38340452 DOI: 10.1016/j.scr.2024.103319Associated cell lines:
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Kaurani L, Islam MR, Heilbronner U, Krüger DM, Zhou J, Methi A, Strauss J, Pradhan R, Schröder S, Burkhardt S, Schuetz AL, Pena T, Erlebach L, Bühler A, Budde M, Senner F, Kohshour MO, Schulte EC, Schmauß M, Reininghaus EZ, Juckel G, Kronenberg-Versteeg D, Delalle I, Odoardi F, Flügel A, Schulze TG, Falkai P, Sananbenesi F, Fischer A
Regulation of Zbp1 by miR-99b-5p in microglia controls the development of schizophrenia-like symptoms in mice
Kaurani L et al. Regulation of Zbp1 by miR-99b-5p in microglia controls the development of schizophrenia-like symptoms in mice. . 2024-04-00. Pubmed ID: 38528182; DOI: 10.1038/s44318-024-00067-8; PMC: PMC11021462 BIONi010-CBIONi037-A 2024-04-00 2024-04-00 PubMed: 38528182 DOI: 10.1038/s44318-024-00067-8Associated cell lines:
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Manibarathi K, Pham T, Hengel H, Synofzik M, Nagel M, Schüle R
An iPSC model for POLR3A-associated spastic ataxia: Generation of three unrelated patient cell lines
Manibarathi K et al. An iPSC model for POLR3A-associated spastic ataxia: Generation of three unrelated patient cell lines. . 2024-04-00. Pubmed ID: 38437768; DOI: 10.1016/j.scr.2024.103363 HIHRSi004-AHIHRSi005-AHIHRSi006-A 2024-04-00 2024-04-00 PubMed: 38437768 DOI: 10.1016/j.scr.2024.103363Associated cell lines:
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Treschow AF, Valente MJ, Lauschke K, Holst B, Andersen AR, Vinggaard AM
Investigating the applicability domain of the hiPSC-based PluriLum assay: an embryotoxicity assessment of chemicals and drugs
Treschow AF et al. Investigating the applicability domain of the hiPSC-based PluriLum assay: an embryotoxicity assessment of chemicals and drugs. . 2024-04-00. Pubmed ID: 38311648; DOI: 10.1007/s00204-023-03675-1; PMC: PMC10944425 BIONi010-C 2024-04-00 2024-04-00 PubMed: 38311648 DOI: 10.1007/s00204-023-03675-1Associated cell lines:
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Webbers SD, Aarts CE, Klein B, Koops D, Geissler J, Tool AT, van Bruggen R, van den Akker E, Kuijpers TW
Reduced myeloid commitment and increased uptake by macrophages of stem cell-derived HPS2 neutrophils
Webbers SD et al. Reduced myeloid commitment and increased uptake by macrophages of stem cell-derived HPS2 neutrophils. . 2024-04-00. Pubmed ID: 38238087; DOI: 10.26508/lsa.202302263; PMC: PMC10796564 SANi009-ASANi010-A 2024-04-00 2024-04-00 PubMed: 38238087 DOI: 10.26508/lsa.202302263 -
Orsi A, Serpieri V, Mazzotta C, Ramusino MC, Rossi E, Cerri S, Valente EM
Generation of iPSC lines derived from skin fibroblasts of two healthy controls using non-transmissible form of Sendai Virus
Orsi A et al. Generation of iPSC lines derived from skin fibroblasts of two healthy controls using non-transmissible form of Sendai Virus. . 2024-04-00. Pubmed ID: 38354648; DOI: 10.1016/j.scr.2024.103332; PMC: PMC10983824 UNIPVi002-AUNIPVi003-A 2024-04-00 2024-04-00 PubMed: 38354648 DOI: 10.1016/j.scr.2024.103332Associated cell lines:
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Liu N, Ge Y, Yang Y, Zhao F, Lv Y, Li Z, Dong R, Liu Y, Gai Z
Human induced pluripotent stem cell line (SDQLCHi064-A) derived from a patient with Canavan disease carrying c.556_559dup GTTC and c.919delA mutations in the ASPA gene
Liu N et al. Human induced pluripotent stem cell line (SDQLCHi064-A) derived from a patient with Canavan disease carrying c.556_559dup GTTC and c.919delA mutations in the ASPA gene. . 2024-04-00. Pubmed ID: 38309148; DOI: 10.1016/j.scr.2024.103325 SDQLCHi064-A 2024-04-00 2024-04-00 PubMed: 38309148 DOI: 10.1016/j.scr.2024.103325Associated cell lines:
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Ovchinnikov DA, Jong S, Cuddy C, Dalby K, Devinsky O, Mullen S, Maljevic S, Petrou S
An iPSC line (FINi003-A) from a male with late-onset developmental and epileptic encephalopathy caused by a heterozygous p.E1211K variant in the SCN2A gene encoding the voltage-gated sodium channel Na(v)1.2
Ovchinnikov DA et al. An iPSC line (FINi003-A) from a male with late-onset developmental and epileptic encephalopathy caused by a heterozygous p.E1211K variant in the SCN2A gene encoding the voltage-gated sodium channel Na(v)1.2. . 2024-04-00. Pubmed ID: 38479087; DOI: 10.1016/j.scr.2024.103367 FINi001-AFINi002-AFINi003-A 2024-04-00 2024-04-00 PubMed: 38479087 DOI: 10.1016/j.scr.2024.103367 -
Punetha Meeti, Saini Sheetal, Chaudhary Suman, Yadav Prem Singh, Whitworth Kristin, Green Jonathan, Kumar Dharmendra, Kues Wilfried A.
Induced Pluripotent Stem Cells in the Era of Precise Genome Editing
Punetha Meeti et al. Induced Pluripotent Stem Cells in the Era of Precise Genome Editing. . 2024-04-00. DOI: 10.2174/1574888x18666230307115326 GIBHi002-AGIBHi002-A-5 2024-04-00 2024-04-00 DOI: 10.2174/1574888x18666230307115326Associated cell lines:
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Cen Y, Zhou T, Chen S, Deng Z, Wang J, Ma N, Zhang S
Generation of an induced pluripotent stem cell line from patient with atrial fibrillation with KCNQ1 p.Ser209Pro mutation
Cen Y et al. Generation of an induced pluripotent stem cell line from patient with atrial fibrillation with KCNQ1 p.Ser209Pro mutation. . 2024-04-00. Pubmed ID: 38341987; DOI: 10.1016/j.scr.2024.103336 GRCHJUi001-A 2024-04-00 2024-04-00 PubMed: 38341987 DOI: 10.1016/j.scr.2024.103336Associated cell lines:
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Zhang X, Xin H, Liu Y, Gai Z, Li Z
An integration-free iPSC line SDQLCHi065-A from a patient with down syndrome, possessing a 47, XY,+21, inv(9)(p12q21),16qh + karyotype
Zhang X et al. An integration-free iPSC line SDQLCHi065-A from a patient with down syndrome, possessing a 47, XY,+21, inv(9)(p12q21),16qh + karyotype. . 2024-04-00. Pubmed ID: 38377649; DOI: 10.1016/j.scr.2024.103351 SDQLCHi065-A 2024-04-00 2024-04-00 PubMed: 38377649 DOI: 10.1016/j.scr.2024.103351Associated cell lines:
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Nielsen AKR, Lilieholm-Røngren L, Schmid B, Holst B, Brodin B, Saaby L
Generation of an iPSC-line (BIONi010C-48) with restored P-glycoprotein functionality following transfection with the human MDR1 gene in the AAVS1 locus
Nielsen AKR et al. Generation of an iPSC-line (BIONi010C-48) with restored P-glycoprotein functionality following transfection with the human MDR1 gene in the AAVS1 locus. . 2024-04-00. Pubmed ID: 38364505; DOI: 10.1016/j.scr.2024.103348 BIONi010-CBIONi010-C-48 2024-04-00 2024-04-00 PubMed: 38364505 DOI: 10.1016/j.scr.2024.103348Associated cell lines:
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Gorrieri G, Tamburro S, Baldassari S, Guerrisi S, Zara F, Ricci E, Maria Cordelli D, Scudieri P, Musante I
Generation of two iPSC lines from Mowat-Wilson syndrome patients carrying heterozygous ZEB2 mutations
Gorrieri G et al. Generation of two iPSC lines from Mowat-Wilson syndrome patients carrying heterozygous ZEB2 mutations. . 2024-04-00. Pubmed ID: 38350246; DOI: 10.1016/j.scr.2024.103333 IGGi004-AIGGi005-A 2024-04-00 2024-04-00 PubMed: 38350246 DOI: 10.1016/j.scr.2024.103333 -
Zhu Q, Wang S, Huang X, Zhao C, Wang Y, Li X, Jia D, Ma C
Understanding the pathogenesis of coronary slow flow: Recent advances
Zhu Q et al. Understanding the pathogenesis of coronary slow flow: Recent advances. . 2024-04-00. Pubmed ID: 36516963; DOI: 10.1016/j.tcm.2022.12.001 SYSUi002-A 2024-04-00 2024-04-00 PubMed: 36516963 DOI: 10.1016/j.tcm.2022.12.001Associated cell lines:
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Souidi Monia, Resta Jessica, Dridi Haikel, Sleiman Yvonne, Reiken Steve, Formoso Karina, Colombani Sarah, Amédro Pascal, Meyer Pierre, Charrabi Azzouz, Vincenti Marie, Liu Yang, Soni Rajesh Kumar, Lezoualc'h Frank, Stéphane Blot D.V.M., Rivier François, Cazorla Olivier, Parini Angelo, Marks Andrew R., Mialet‐Perez Jeanne, Lacampagne Alain, Meli Albano C.
Ryanodine receptor dysfunction causes senescence and fibrosis in Duchenne dilated cardiomyopathy
Souidi Monia et al. Ryanodine receptor dysfunction causes senescence and fibrosis in Duchenne dilated cardiomyopathy. . 2024-04-00. DOI: 10.1002/jcsm.13411 INSRMi008-AINSRMi009-AINSRMi010-A 2024-04-00 2024-04-00 DOI: 10.1002/jcsm.13411Associated cell lines:
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Yin T, Qian Y, Zhang X, Liao Y, Wu B, Wang S, Wang H
Derivation of an induced pluripotent stem cell line (FDCHi014-A) from PBMCs of a seven-year-old patient with a truncating NOVA2 variant (c.625del)
Yin T et al. Derivation of an induced pluripotent stem cell line (FDCHi014-A) from PBMCs of a seven-year-old patient with a truncating NOVA2 variant (c.625del). . 2024-04-00. Pubmed ID: 38430735; DOI: 10.1016/j.scr.2024.103369 FDCHi014-A 2024-04-00 2024-04-00 PubMed: 38430735 DOI: 10.1016/j.scr.2024.103369Associated cell lines:
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Shi Z, Liu H, Feng F, Huang Z, Chen WX
Generation of an induced pluripotent stem cell line GWCMCi006-A from a patient with autosomal dominant neurodevelopmental disorder with or without hyperkinetic movements and seizures harboring GRIN1 c.389A > G mutation
Shi Z et al. Generation of an induced pluripotent stem cell line GWCMCi006-A from a patient with autosomal dominant neurodevelopmental disorder with or without hyperkinetic movements and seizures harboring GRIN1 c.389A > G mutation. . 2024-04-00. Pubmed ID: 38452705; DOI: 10.1016/j.scr.2024.103371 GWCMCi005-AGWCMCi006-A 2024-04-00 2024-04-00 PubMed: 38452705 DOI: 10.1016/j.scr.2024.103371Associated cell lines:
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Liu Jiabin, Tan Jieqiong, Tang Beisha, Guo Jifeng
Unveiling the role of iPLA2β in neurodegeneration: From molecular mechanisms to advanced therapies
Liu Jiabin et al. Unveiling the role of iPLA2β in neurodegeneration: From molecular mechanisms to advanced therapies. . 2024-04-00. DOI: 10.1016/j.phrs.2024.107114 IBMSi012-AONHi001-ALNDWCHi001-A 2024-04-00 2024-04-00 DOI: 10.1016/j.phrs.2024.107114Associated cell lines:
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Kamand M, Taleb R, Wathikthinnakon M, Mohamed FA, Ghazanfari SP, Konstantinov D, Hald JL, Holst B, Brasch-Andersen C, Møller RS, Lemke JR, Krey I, Freude K, Chandrasekaran A
Generation of two patient specific GABRD variants and their isogenic controls for modeling epilepsy
Kamand M et al. Generation of two patient specific GABRD variants and their isogenic controls for modeling epilepsy. . 2024-04-00. Pubmed ID: 38458029; DOI: 10.1016/j.scr.2024.103372 KUi012-AKUi013-AKUi013-A-1 2024-04-00 2024-04-00 PubMed: 38458029 DOI: 10.1016/j.scr.2024.103372Associated cell lines:
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Gao C, Yang X, Yang Y, Liu N, Li Y, Liu Y, Gai Z
Generation of an induced pluripotent stem cell line (SDQLCHi067-A) from a patient with subcortical band heterotopia harboring a heterozygous mutation in DCX gene
Gao C et al. Generation of an induced pluripotent stem cell line (SDQLCHi067-A) from a patient with subcortical band heterotopia harboring a heterozygous mutation in DCX gene. . 2024-04-00. Pubmed ID: 38402847; DOI: 10.1016/j.scr.2024.103356 SDQLCHi067-A 2024-04-00 2024-04-00 PubMed: 38402847 DOI: 10.1016/j.scr.2024.103356Associated cell lines:
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Ribeiro M, Jager J, Furtado M, Carvalho T, Cabral JMS, Brito D, Carmo-Fonseca M, Martins S, da Rocha ST
Generation of induced pluripotent stem cell lines from two unrelated individuals with familial hypertrophic cardiomyopathy carrying MYBPC3 nonsense mutations
Ribeiro M et al. Generation of induced pluripotent stem cell lines from two unrelated individuals with familial hypertrophic cardiomyopathy carrying MYBPC3 nonsense mutations. . 2024-04-00. Pubmed ID: 38417376; DOI: 10.1016/j.scr.2024.103362 IBBISTi007-AIBBISTi007-BIBBISTi008-AIBBISTi008-B 2024-04-00 2024-04-00 PubMed: 38417376 DOI: 10.1016/j.scr.2024.103362Associated cell lines:
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Lei Q, Zhou W, Huang L, Zhang Y, Xu X, Guo X
Establishing a human-induced pluripotent stem cell line (SMUSHi003-A) from a patient with Charcot-Marie-Tooth disease and focal segmental glomerulosclerosis
Lei Q et al. Establishing a human-induced pluripotent stem cell line (SMUSHi003-A) from a patient with Charcot-Marie-Tooth disease and focal segmental glomerulosclerosis. . 2024-04-00. Pubmed ID: 38412658; DOI: 10.1016/j.scr.2024.103357 SMUSHi003-A 2024-04-00 2024-04-00 PubMed: 38412658 DOI: 10.1016/j.scr.2024.103357Associated cell lines:
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Baek D, Lee KG, Sohn HY, Park JH, Lee HK, Bayarsaikhan G, Yoo SW, Lee B, Kim JS, Koh YH, Kwon M
Generation of an induced pluripotent stem cell line (KNIHi001-A) by reprogramming peripheral blood mononuclear cells isolated from a patient with Parkinson's disease
Baek D et al. Generation of an induced pluripotent stem cell line (KNIHi001-A) by reprogramming peripheral blood mononuclear cells isolated from a patient with Parkinson's disease. . 2024-04-00. Pubmed ID: 38447455; DOI: 10.1016/j.scr.2024.103358 KNIHi001-A 2024-04-00 2024-04-00 PubMed: 38447455 DOI: 10.1016/j.scr.2024.103358Associated cell lines:
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Segura-Tudela Alejandro, López-Nevado Marta, Nieto-López Celia, García-Jiménez Sandra, Díaz-Madroñero María J., Delgado Ángeles, Cabrera-Marante Oscar, Pleguezuelo Daniel, Morales Pablo, Paz-Artal Estela, Gil-Niño Jorge, Marco Francisco M., Serrano Cristina, González-Granado Luis I., Quesada-Espinosa Juan F., Allende Luis M.
Enrichment of Immune Dysregulation Disorders in Adult Patients with Human Inborn Errors of Immunity
Segura-Tudela Alejandro et al. Enrichment of Immune Dysregulation Disorders in Adult Patients with Human Inborn Errors of Immunity. . 2024-04-00. DOI: 10.1007/s10875-024-01664-2 CVTTHi001-A 2024-04-00 2024-04-00 DOI: 10.1007/s10875-024-01664-2Associated cell lines:
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Agrawal T, Maddileti S, Verma A, Kaliki S, Mariappan I
Generation of an induced pluripotent stem cell line (LVPEIi002-A) with heterozygous RB1 mutation using peri-orbital fat derived mesenchymal cells of a patient with inherited retinoblastoma
Agrawal T et al. Generation of an induced pluripotent stem cell line (LVPEIi002-A) with heterozygous RB1 mutation using peri-orbital fat derived mesenchymal cells of a patient with inherited retinoblastoma. . 2024-04-00. Pubmed ID: 38335663; DOI: 10.1016/j.scr.2024.103329 LVPEIi002-ARUCDRi002-A-63RUCDRi002-A-64RUCDRi002-A-65 2024-04-00 2024-04-00 PubMed: 38335663 DOI: 10.1016/j.scr.2024.103329Associated cell lines:
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Flores-Ponce X, López-Ornelas A, Escobedo-Avila I, Rodríguez-Violante M, Dávila-Ortiz de Montellano D, Cervantes-Arriaga A, Monroy-Jaramillo N, Campos-Romo A, Velasco I
Establishment of induced pluripotent stem cell lines derived from Parkinson's disease Mexican patients: A sporadic (UNAMi002-A) and a familial (UNAMi003-A) case carrying a mutation in PINK1
Flores-Ponce X et al. Establishment of induced pluripotent stem cell lines derived from Parkinson's disease Mexican patients: A sporadic (UNAMi002-A) and a familial (UNAMi003-A) case carrying a mutation in PINK1. . 2024-04-00. Pubmed ID: 38359473; DOI: 10.1016/j.scr.2024.103337 UNAMi002-AUNAMi003-A 2024-04-00 2024-04-00 PubMed: 38359473 DOI: 10.1016/j.scr.2024.103337Associated cell lines:
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Fang R, Guo X, Feng J, Chen Q, Wang T, Ma J
Generation of an induced pluripotent stem cell line (SYSUSCi004-A) from a patient with Infantile Malignant Osteopetrosis
Fang R et al. Generation of an induced pluripotent stem cell line (SYSUSCi004-A) from a patient with Infantile Malignant Osteopetrosis. . 2024-04-00. Pubmed ID: 38335662; DOI: 10.1016/j.scr.2024.103330 SYSUSCi004-A 2024-04-00 2024-04-00 PubMed: 38335662 DOI: 10.1016/j.scr.2024.103330Associated cell lines:
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Liu Yue, Tang Yanhui, Zhang Hui, Chen Hongying, Luo Qing, Liu Jinbo
Duchenne muscular dystrophy caused by a deletion (c.5021del) in exon 35 of the DMD gene: A case report and review of the literature
Liu Yue et al. Duchenne muscular dystrophy caused by a deletion (c.5021del) in exon 35 of the DMD gene: A case report and review of the literature. . 2024-04-00. DOI: 10.1016/j.heliyon.2024.e28677 SDQLCHi007-A 2024-04-00 2024-04-00 DOI: 10.1016/j.heliyon.2024.e28677Associated cell lines:
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Duff C, Islam M, Gagliano O, Pramod H, Rashidi H, Kurian MA, Gissen P, Baruteau J
Generation of induced pluripotent stem cells (UCLi024-A) from a patient with argininosuccinate lyase deficiency carrying a homozygous c.437G > A (p.Arg146Gln) mutation
Duff C et al. Generation of induced pluripotent stem cells (UCLi024-A) from a patient with argininosuccinate lyase deficiency carrying a homozygous c.437G > A (p.Arg146Gln) mutation. . 2024-04-00. Pubmed ID: 38422816; DOI: 10.1016/j.scr.2024.103365 UCLi024-A 2024-04-00 2024-04-00 PubMed: 38422816 DOI: 10.1016/j.scr.2024.103365Associated cell lines:
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Li SA, Zhang YJ, Zhu YQ, Meng XY, Chen CL, Liu PP, Sun W
Generation of induced pluripotent stem cells (ZZUCSBi001-A) from skin fibroblasts of a healthy donor
Li SA et al. Generation of induced pluripotent stem cells (ZZUCSBi001-A) from skin fibroblasts of a healthy donor. . 2024-04-00. Pubmed ID: 38335661; DOI: 10.1016/j.scr.2024.103328 ZZUi011-AZZUi019-AZZUi031-AZZUCSBi001-A 2024-04-00 2024-04-00 PubMed: 38335661 DOI: 10.1016/j.scr.2024.103328Associated cell lines:
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Mikhailova V., Kondratyev N., Alfimova M., Kaleda V., Lezheiko T., Ublinsky M., Ushakov V., Lebedeva I., Galiakberova A., Artyuhov A., Dashinimaev E., Golimbet V.
The SLC6A1 Mutation Schizophrenia case — A Comprehensive Case Study With iPSC Generation
Mikhailova V. et al. The SLC6A1 Mutation Schizophrenia case — A Comprehensive Case Study With iPSC Generation. . 2024-04-00. DOI: 10.1192/j.eurpsy.2024.1592 MHRCCGi001-AMHRCCGi004-AMHRCCGi005-A 2024-04-00 2024-04-00 DOI: 10.1192/j.eurpsy.2024.1592Associated cell lines:
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Cukier HN, Simon SA, Tang E, Golightly CG, Laverde-Paz MJ, Adams LD, Starks TD, Vance JM, Cuccaro ML, Haines JL, Byrd GS, Pericak-Vance MA, Dykxhoorn DM
Generation of an induced pluripotent stem cell line (UMi043-A) from an African American patient with Alzheimer's disease carrying an ABCA7 deletion (p.Arg578Alafs)
Cukier HN et al. Generation of an induced pluripotent stem cell line (UMi043-A) from an African American patient with Alzheimer's disease carrying an ABCA7 deletion (p.Arg578Alafs). . 2024-04-00. Pubmed ID: 38422817; DOI: 10.1016/j.scr.2024.103364 UMi043-A 2024-04-00 2024-04-00 PubMed: 38422817 DOI: 10.1016/j.scr.2024.103364Associated cell lines:
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Pierre B, Laëtitia DB, Camille B, Claire P, Elise B, Estelle G, Vincent F, Eric V
Generation of CRISPR/Cas9 edited human induced pluripotent stem cell line carrying the heterozygous p.H695VfsX5 frameshift mutation in the exon 10 of the PKP2 gene
Pierre B et al. Generation of CRISPR/Cas9 edited human induced pluripotent stem cell line carrying the heterozygous p.H695VfsX5 frameshift mutation in the exon 10 of the PKP2 gene. . 2024-04-00. Pubmed ID: 38382214; DOI: 10.1016/j.scr.2024.103341 ICANi002-AICANi002-A-5 2024-04-00 2024-04-00 PubMed: 38382214 DOI: 10.1016/j.scr.2024.103341Associated cell lines:
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Boullé M, Boucharlat A, Leleu A, Banal C, Coussement A, Hollenstein M, Yates F, Lefort N, Agou F
Generation of IPi001-A/B/C human induced pluripotent stem cell lines from healthy amniotic fluid cells
Boullé M et al. Generation of IPi001-A/B/C human induced pluripotent stem cell lines from healthy amniotic fluid cells. . 2024-04-00. Pubmed ID: 38387169; DOI: 10.1016/j.scr.2024.103350 IPi001-AIPi001-BIPi001-C 2024-04-00 2024-04-00 PubMed: 38387169 DOI: 10.1016/j.scr.2024.103350 -
Zhang H, Liu C, Liu Y, Gai Z
Establishment of human induced pluripotent stem cell line SDQLCHi029-A from one Type 1 familial glucocorticoid deficiency patient carrying compound heterozygote mutations in MC2R gene
Zhang H et al. Establishment of human induced pluripotent stem cell line SDQLCHi029-A from one Type 1 familial glucocorticoid deficiency patient carrying compound heterozygote mutations in MC2R gene. . 2024-04-00. Pubmed ID: 38430736; DOI: 10.1016/j.scr.2024.103368 SDQLCHi029-A 2024-04-00 2024-04-00 PubMed: 38430736 DOI: 10.1016/j.scr.2024.103368Associated cell lines:
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Przymuszała M, Martyniak A, Kwiatkowska J, Meyer-Szary J, Śledzińska K, Wierzba J, Dulak J, Florczyk-Soluch U, Stępniewski J
Generation of human induced pluripotent stem cell line derived from Becker muscular dystrophy patient with CRISPR/Cas9-mediated correction of DMD gene mutation
Przymuszała M et al. Generation of human induced pluripotent stem cell line derived from Becker muscular dystrophy patient with CRISPR/Cas9-mediated correction of DMD gene mutation. . 2024-04-00. Pubmed ID: 38324931; DOI: 10.1016/j.scr.2024.103327 DMBi009-ADMBi009-A-1 2024-04-00 2024-04-00 PubMed: 38324931 DOI: 10.1016/j.scr.2024.103327Associated cell lines:
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Jin H, Fu H, Wang J, Wang Z, Liu J, Han F, Zheng H, Jiang Y
Generation of a DMD loss-of-function mutant human embryonic stem cell lines by CRISPR base editing
Jin H et al. Generation of a DMD loss-of-function mutant human embryonic stem cell lines by CRISPR base editing. . 2024-04-00. Pubmed ID: 38428348; DOI: 10.1016/j.scr.2024.103343 WAe009-A-1C 2024-04-00 2024-04-00 PubMed: 38428348 DOI: 10.1016/j.scr.2024.103343Associated cell lines:
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Li J, Jiang J, Ye L, Lian Z, Gong H, Lei W, Dai Y, Hu S
Generation of human induced pluripotent stem cell line from a patient with restrictive cardiomyopathy
Li J et al. Generation of human induced pluripotent stem cell line from a patient with restrictive cardiomyopathy. . 2024-04-00. Pubmed ID: 38428347; DOI: 10.1016/j.scr.2024.103370 ICSSUi004-A 2024-04-00 2024-04-00 PubMed: 38428347 DOI: 10.1016/j.scr.2024.103370Associated cell lines:
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Fasciani I, Petragnano F, Wang Z, Edwards R, Telugu N, Pietrantoni I, Zabel U, Zauber H, Grieben M, Terzenidou ME, Di Gregorio J, Pellegrini C, Santini S Jr, Taddei AR, Pohl B, Aringhieri S, Carli M, Aloisi G, Marampon F, Charlesworth E, Roman A, Diecke S, Flati V, Giorgi F, Amicarelli F, Tobin AB, Scarselli M, Tokatlidis K, Rossi M, Lohse MJ, Annibale P, Maggio R
The C-terminus of the prototypical M2 muscarinic receptor localizes to the mitochondria and regulates cell respiration under stress conditions
Fasciani I et al. The C-terminus of the prototypical M2 muscarinic receptor localizes to the mitochondria and regulates cell respiration under stress conditions. . 2024-04-00. Pubmed ID: 38683874; DOI: 10.1371/journal.pbio.3002582; PMC: PMC11093360 BIHi005-AMDCi014-AMDCi014-BBIHi005-A-39 2024-04-00 2024-04-00 PubMed: 38683874 DOI: 10.1371/journal.pbio.3002582Associated cell lines:
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Joanne P, Hovhannisyan Y, Simon A, Revet G, Diot R, Friob G, Calin D, Li Z, Béhin A, Wahbi K, Tachdjian G, Agbulut O
Generation of human induced pluripotent stem cell lines from five patients with Myofibrillar myopathy carrying different heterozygous mutations in the DES gene
Joanne P et al. Generation of human induced pluripotent stem cell lines from five patients with Myofibrillar myopathy carrying different heterozygous mutations in the DES gene. . 2024-04-00. Pubmed ID: 38354647; DOI: 10.1016/j.scr.2024.103338 INSRMi012-CINSRMi013-AINSRMi019-AINSRMi020-AINSRMi021-A 2024-04-00 2024-04-00 PubMed: 38354647 DOI: 10.1016/j.scr.2024.103338Associated cell lines:
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Conteduca G, Baldo C, Arado A, da Silva JSM, Testa B, Baldassari S, Zara F, Filaci G, Coviello D, Malacarne M
Generation of IGGi003-A induced pluripotent stem cell line from a patient with Sotos Syndrome carrying c.1633delA NSD1 variant in exon 5
Conteduca G et al. Generation of IGGi003-A induced pluripotent stem cell line from a patient with Sotos Syndrome carrying c.1633delA NSD1 variant in exon 5. . 2024-04-00. Pubmed ID: 38301425; DOI: 10.1016/j.scr.2024.103324 IGGi003-A 2024-04-00 2024-04-00 PubMed: 38301425 DOI: 10.1016/j.scr.2024.103324Associated cell lines:
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Ahmad I, Kapoor H, Srivastava AK, Faruq M
Generation of two human induced pluripotent stem cell lines, IGIBi012-A and IGIBi013-A from Friedreich's ataxia (FRDA) patients with homozygous GAA repeat expansion in FXN gene
Ahmad I et al. Generation of two human induced pluripotent stem cell lines, IGIBi012-A and IGIBi013-A from Friedreich's ataxia (FRDA) patients with homozygous GAA repeat expansion in FXN gene. . 2024-04-00. Pubmed ID: 38367363; DOI: 10.1016/j.scr.2024.103340 IGIBi006-AIGIBi008-AIGIBi012-AIGIBi013-A 2024-04-00 2024-04-00 PubMed: 38367363 DOI: 10.1016/j.scr.2024.103340Associated cell lines:
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Ou-Yang CH, Chen PS, Lin CH
Generation of a human induced pluripotent stem cell line NTUHi004-A from a patient with Leigh syndrome harboring a homozygous missense mutation c.836 T > G (p.Met279Arg) in NDUFAF5 gene
Ou-Yang CH et al. Generation of a human induced pluripotent stem cell line NTUHi004-A from a patient with Leigh syndrome harboring a homozygous missense mutation c.836 T > G (p.Met279Arg) in NDUFAF5 gene. . 2024-04-00. Pubmed ID: 38458030; DOI: 10.1016/j.scr.2024.103379 NTUHi004-A 2024-04-00 2024-04-00 PubMed: 38458030 DOI: 10.1016/j.scr.2024.103379Associated cell lines:
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Luong TH, Pham TA, Nhung Nguyen TH, Nguyen XH
Generation of induced pluripotent stem cell line (VRISGi004-A) from a healthy female donor by reprogramming erythroid progenitor cells
Luong TH et al. Generation of induced pluripotent stem cell line (VRISGi004-A) from a healthy female donor by reprogramming erythroid progenitor cells. . 2024-04-00. Pubmed ID: 38341988; DOI: 10.1016/j.scr.2024.103331 VRISGi002-AVRISGi004-A 2024-04-00 2024-04-00 PubMed: 38341988 DOI: 10.1016/j.scr.2024.103331Associated cell lines:
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Ferreira LGA, Cabral-da-Silva MC, Pachernegg S, van den Bergen JA, Robevska G, Vlahos K, Howden SE, Ng ES, Dias-da-Silva MR, Sinclair AH, Ayers KL
Generation of heterozygous (MCRIi030-A-1) and homozygous (MCRIi030-A-2) NR2F2/COUP-TFII knockout human iPSC lines
Ferreira LGA et al. Generation of heterozygous (MCRIi030-A-1) and homozygous (MCRIi030-A-2) NR2F2/COUP-TFII knockout human iPSC lines. . 2024-04-00. Pubmed ID: 38458031; DOI: 10.1016/j.scr.2024.103374 MCRIi030-AMCRIi030-A-1MCRIi030-A-2 2024-04-00 2024-04-00 PubMed: 38458031 DOI: 10.1016/j.scr.2024.103374Associated cell lines:
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Cubillos P, Ditzer N, Kolodziejczyk A, Schwenk G, Hoffmann J, Schütze TM, Derihaci RP, Birdir C, Köllner JE, Petzold A, Sarov M, Martin U, Long KR, Wimberger P, Albert M
The growth factor EPIREGULIN promotes basal progenitor cell proliferation in the developing neocortex
Cubillos P et al. The growth factor EPIREGULIN promotes basal progenitor cell proliferation in the developing neocortex. . 2024-04-00. Pubmed ID: 38514807; DOI: 10.1038/s44318-024-00068-7; PMC: PMC11021537 CRTDi004-A 2024-04-00 2024-04-00 PubMed: 38514807 DOI: 10.1038/s44318-024-00068-7Associated cell lines:
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Daya NM, Döring K, Zhuge H, Volke L, Stab V, Dietz J, Athamneh M, Roos A, Zaehres H, Güttsches AK, Mavrommatis L, Vorgerd M
Generation of two hiPSCs lines of two patients carrying truncating mutations in the dimerization domain of filamin C
Daya NM et al. Generation of two hiPSCs lines of two patients carrying truncating mutations in the dimerization domain of filamin C. . 2024-04-00. Pubmed ID: 38309149; DOI: 10.1016/j.scr.2024.103320 HIMRi001-AHIMRi004-AHIMRi005-A 2024-04-00 2024-04-00 PubMed: 38309149 DOI: 10.1016/j.scr.2024.103320Associated cell lines:
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Wu Y, Zhang T, Chen Z, Tang L, Zhang L, Chen J, Wan X, Sun X
Establishment of the induced pluripotent stem cell line SJTUGHi002-A from a CNGA1-related recessive retinitis pigmentosa patient
Wu Y et al. Establishment of the induced pluripotent stem cell line SJTUGHi002-A from a CNGA1-related recessive retinitis pigmentosa patient. . 2024-04-00. Pubmed ID: 38340451; DOI: 10.1016/j.scr.2024.103334 SJTUGHi002-A 2024-04-00 2024-04-00 PubMed: 38340451 DOI: 10.1016/j.scr.2024.103334Associated cell lines:
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Ludwik KA, Hellwig L, Fisch T, Contzen J, Schaar C, Mergenthaler P, Stachelscheid H
Generation of two human induced pluripotent stem cell lines with BAX and BAK1 double knock-out using CRISPR/Cas9
Ludwik KA et al. Generation of two human induced pluripotent stem cell lines with BAX and BAK1 double knock-out using CRISPR/Cas9. . 2024-04-00. Pubmed ID: 38460306; DOI: 10.1016/j.scr.2024.103377 BIHi005-ABIHi250-ABIHi005-A-15BIHi005-A-17BIHi005-A-20BIHi250-A-1BIHi250-A-2BIHi250-A-4 2024-04-00 2024-04-00 PubMed: 38460306 DOI: 10.1016/j.scr.2024.103377Associated cell lines:
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Agrawal T, Maddileti S, Mariappan I
Generation and characterization of three CRISPR/Cas9 edited RB1 null hiPSC lines for retinoblastoma disease modelling
Agrawal T et al. Generation and characterization of three CRISPR/Cas9 edited RB1 null hiPSC lines for retinoblastoma disease modelling. . 2024-04-00. Pubmed ID: 38452707; DOI: 10.1016/j.scr.2024.103373 LVPEIi002-ARUCDRi002-A-63RUCDRi002-A-64RUCDRi002-A-65 2024-04-00 2024-04-00 PubMed: 38452707 DOI: 10.1016/j.scr.2024.103373Associated cell lines:
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Ishikawa KI, Okuzumi A, Yoshino H, Hattori N, Akamatsu W
Generation of hiPSCs (JUCGRMi003-A) from a patient with Parkinson's disease with PARK2 mutation
Ishikawa KI et al. Generation of hiPSCs (JUCGRMi003-A) from a patient with Parkinson's disease with PARK2 mutation. . 2024-04-00. Pubmed ID: 38309147; DOI: 10.1016/j.scr.2024.103323 JUCGRMi003-A 2024-04-00 2024-04-00 PubMed: 38309147 DOI: 10.1016/j.scr.2024.103323Associated cell lines:
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Guan J, Shen L, Liu C, Lv Y, Zhang H, Liu Y, Gai Z
Establishment of iPS cell line (SDQLCHi061-A) from a patient with carbamoylphosphate synthetase I deficiency due to CPS1 mutation
Guan J et al. Establishment of iPS cell line (SDQLCHi061-A) from a patient with carbamoylphosphate synthetase I deficiency due to CPS1 mutation. . 2024-04-00. Pubmed ID: 38394969; DOI: 10.1016/j.scr.2024.103353 SDQLCHi021-ASDQLCHi061-A 2024-04-00 2024-04-00 PubMed: 38394969 DOI: 10.1016/j.scr.2024.103353Associated cell lines:
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Liu N, Zhang Y, Dong R, Lv Y, Gao M, Yang X, Liu Y, Gai Z
Generation of a human induced pluripotent stem cell line (SDQLCHi057-A) from an Isovaleric aciduria patient carrying novel compound heterozygous mutations in the IVD gene
Liu N et al. Generation of a human induced pluripotent stem cell line (SDQLCHi057-A) from an Isovaleric aciduria patient carrying novel compound heterozygous mutations in the IVD gene. . 2024-04-00. Pubmed ID: 38401345; DOI: 10.1016/j.scr.2024.103314 SDQLCHi040-ASDQLCHi057-A 2024-04-00 2024-04-00 PubMed: 38401345 DOI: 10.1016/j.scr.2024.103314Associated cell lines:
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Yang Y, Liu C, Liu N, Yang X, Liu Y, Gai Z
Generation and characterization of PBMCs-derived human induced pluripotent stem cell (iPSC) line SDQLCHi055-A from a patient with NEDSDV carrying a heterozygote mutation in the CTNNB1 gene
Yang Y et al. Generation and characterization of PBMCs-derived human induced pluripotent stem cell (iPSC) line SDQLCHi055-A from a patient with NEDSDV carrying a heterozygote mutation in the CTNNB1 gene. . 2024-04-00. Pubmed ID: 38364504; DOI: 10.1016/j.scr.2024.103335 SDQLCHi055-A 2024-04-00 2024-04-00 PubMed: 38364504 DOI: 10.1016/j.scr.2024.103335Associated cell lines:
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Huang Wenjun, Zhou Rui, Jiang Congshan, Wang Jie, Zhou Yafei, Xu Xiaoyan, Wang Tao, Li Anmao, Zhang Yanmin
Mitochondrial dysfunction is associated with hypertrophic cardiomyopathy in Pompe disease‐specific induced pluripotent stem cell‐derived cardiomyocytes
Huang Wenjun et al. Mitochondrial dysfunction is associated with hypertrophic cardiomyopathy in Pompe disease‐specific induced pluripotent stem cell‐derived cardiomyocytes. . 2024-04-00. DOI: 10.1111/cpr.13573 XACHi005-AXACHi006-A 2024-04-00 2024-04-00 DOI: 10.1111/cpr.13573Associated cell lines:
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Pierre M, Jauvin D, Puymirat J, Boutjdir M, Chahine M
Generation of three myotonic dystrophy type 1 patient iPSC lines (CBRCULi018-A, CBRCULi019-A, CBRCULi020-A) derived from lymphoblastoid cell lines for disease modelling and therapeutic research
Pierre M et al. Generation of three myotonic dystrophy type 1 patient iPSC lines (CBRCULi018-A, CBRCULi019-A, CBRCULi020-A) derived from lymphoblastoid cell lines for disease modelling and therapeutic research. . 2024-04-00. Pubmed ID: 38490135; DOI: 10.1016/j.scr.2024.103375 CBRCULi001-ACBRCULi002-ACBRCULi003-ACBRCULi004-ACBRCULi005-ACBRCULi006-ACBRCULi007-ACBRCULi018-ACBRCULi019-ACBRCULi020-A 2024-04-00 2024-04-00 PubMed: 38490135 DOI: 10.1016/j.scr.2024.103375Associated cell lines:
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Hou X, Fan W, Zeng J, Gao Z, Wan J, Liao B
Generation of a ISL1 homozygous knockout stem cell line (WAe009-A-1G) by episomal vector-based CRISPR/Cas9 system
Hou X et al. Generation of a ISL1 homozygous knockout stem cell line (WAe009-A-1G) by episomal vector-based CRISPR/Cas9 system. . 2024-04-00. Pubmed ID: 38452706; DOI: 10.1016/j.scr.2024.103376 WAe009-AWAe009-A-1G 2024-04-00 2024-04-00 PubMed: 38452706 DOI: 10.1016/j.scr.2024.103376Associated cell lines:
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Hua M, Williams L, Burns K, Liu S, Ellis J, Innes AM, McPherson M, Yang G
Generation and characterization of a human iPSC line and gene-corrected isogenic line derived from a patient with a CELF2 gene mutation
Hua M et al. Generation and characterization of a human iPSC line and gene-corrected isogenic line derived from a patient with a CELF2 gene mutation. . 2024-04-00. Pubmed ID: 38364506; DOI: 10.1016/j.scr.2024.103344 UOCi003-AUOCi003-A-1 2024-04-00 2024-04-00 PubMed: 38364506 DOI: 10.1016/j.scr.2024.103344Associated cell lines:
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Ge Y, Cheng Y, Yin T, Peng X, Xiong Z, Wu B, Wang H, Xiong M, Zhou W
Generation of a human induced pluripotent stem cell line (FDCHi012-A) from a patient with DYRK1A-related intellectual disability syndrome carrying DYRK1A mutation (c.1024G > T)
Ge Y et al. Generation of a human induced pluripotent stem cell line (FDCHi012-A) from a patient with DYRK1A-related intellectual disability syndrome carrying DYRK1A mutation (c.1024G > T). . 2024-04-00. Pubmed ID: 38382213; DOI: 10.1016/j.scr.2024.103345 FDCHi012-A 2024-04-00 2024-04-00 PubMed: 38382213 DOI: 10.1016/j.scr.2024.103345Associated cell lines:
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Sun Y, Zhao H, Yang S, Wang G, Zhu L, Sun C, An Y
Urine-derived stem cells: Promising advancements and applications in regenerative medicine and beyond
Sun Y et al. Urine-derived stem cells: Promising advancements and applications in regenerative medicine and beyond. . 2024-03-30. Pubmed ID: 38509987; DOI: 10.1016/j.heliyon.2024.e27306; PMC: PMC10951541 WMUi017-A 2024-03-30 2024-03-30 PubMed: 38509987 DOI: 10.1016/j.heliyon.2024.e27306Associated cell lines:
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Suárez-Herrera N, Li CHZ, Leijsten N, Karjosukarso DW, Corradi Z, Bukkems F, Duijkers L, Cremers FPM, Hoyng CB, Garanto A, Collin RWJ
Preclinical Development of Antisense Oligonucleotides to Rescue Aberrant Splicing Caused by an Ultrarare ABCA4 Variant in a Child with Early-Onset Stargardt Disease
Suárez-Herrera N et al. Preclinical Development of Antisense Oligonucleotides to Rescue Aberrant Splicing Caused by an Ultrarare ABCA4 Variant in a Child with Early-Onset Stargardt Disease. . 2024-03-29. Pubmed ID: 38607040; DOI: 10.3390/cells13070601; PMC: PMC11011354 RMCGENi021-A 2024-03-29 2024-03-29 PubMed: 38607040 DOI: 10.3390/cells13070601Associated cell lines:
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Venhuizen Jeron, van Bergen Maaike G. J. M., Bergevoet Saskia M., Gilissen Daan, Spruijt Cornelia G., Wingens Laura, van den Akker Emile, Vermeulen Michiel, Jansen Joop H., Martens Joost H. A., van der Reijden Bert A.
GFI1B and LSD1 repress myeloid traits during megakaryocyte differentiation
Venhuizen Jeron et al. GFI1B and LSD1 repress myeloid traits during megakaryocyte differentiation. . 2024-03-28. DOI: 10.1038/s42003-024-06090-z SANi005-A 2024-03-28 2024-03-28 DOI: 10.1038/s42003-024-06090-zAssociated cell lines:
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Yarkova ES, Grigor'eva EV, Medvedev SP, Tarasevich DA, Pavlova SV, Valetdinova KR, Minina JM, Zakian SM, Malakhova AA
Detection of ER Stress in iPSC-Derived Neurons Carrying the p.N370S Mutation in the GBA1 Gene
Yarkova ES et al. Detection of ER Stress in iPSC-Derived Neurons Carrying the p.N370S Mutation in the GBA1 Gene. . 2024-03-27. Pubmed ID: 38672099; DOI: 10.3390/biomedicines12040744; PMC: PMC11047942 ICGi021-AICGi022-AICGi034-AICGi039-AICGi039-BICGi039-CICGi034-A-1ICGi034-A-2ICGi034-A-3ICGi034-A-4ICGi034-DICGi034-EICGi022-BICGi021-A-6ICGi021-A-7 2024-03-27 2024-03-27 PubMed: 38672099 DOI: 10.3390/biomedicines12040744Associated cell lines:
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Ullmann K, Manstein F, Triebert W, Kriedemann N, Franke A, Teske J, Mertens M, Lupanow V, Göhring G, Haase A, Martin U, Zweigerdt R
Matrix-free human pluripotent stem cell manufacturing by seed train approach and intermediate cryopreservation
Ullmann K et al. Matrix-free human pluripotent stem cell manufacturing by seed train approach and intermediate cryopreservation. . 2024-03-25. Pubmed ID: 38528578; DOI: 10.1186/s13287-024-03699-z; PMC: PMC10964510 MHHi006-AMHHi008-A 2024-03-25 2024-03-25 PubMed: 38528578 DOI: 10.1186/s13287-024-03699-z -
Zhang X.
Analysis of Fundamental Research Status and Strategy of Funding Profile of Myopia of the National Natural Science Foundation of China
Zhang X.. Analysis of Fundamental Research Status and Strategy of Funding Profile of Myopia of the National Natural Science Foundation of China. . 2024-03-25. DOI: 10.3760/cma.j.cn115909-20231207-00216 FDEENTi003-A 2024-03-25 2024-03-25 DOI: 10.3760/cma.j.cn115909-20231207-00216Associated cell lines:
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Hansen Cathrin E., Kamermans Alwin, Mol Kevin, Berve Kristina, Rodriguez-Mogeda Carla, Fung Wing Ka, van het Hof Bert, Fontijn Ruud D., van der Pol Susanne M. A., Michalick Laura, Kuebler Wolfgang M., Kenkhuis Boyd, van Roon-Mom Willeke, Liedtke Wolfgang, Engelhardt Britta, Kooij Gijs, Witte Maarten E., de Vries Helga E.
Inflammation-induced TRPV4 channels exacerbate blood–brain barrier dysfunction in multiple sclerosis
Hansen Cathrin E. et al. Inflammation-induced TRPV4 channels exacerbate blood–brain barrier dysfunction in multiple sclerosis. . 2024-03-23. DOI: 10.1186/s12974-024-03069-9 LUMCi002-ALUMCi003-A 2024-03-23 2024-03-23 DOI: 10.1186/s12974-024-03069-9Associated cell lines:
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Xavier G, Navarrete Santos A, Hartmann C, Santoro ML, Flegel N, Reinsch J, Majer A, Ehrhardt T, Pfeifer J, Simm A, Hollemann T, Belangero SI, Rujescu D, Jung M
Comparison of Extracellular Vesicles from Induced Pluripotent Stem Cell-Derived Brain Cells
Xavier G et al. Comparison of Extracellular Vesicles from Induced Pluripotent Stem Cell-Derived Brain Cells. . 2024-03-22. Pubmed ID: 38612385; DOI: 10.3390/ijms25073575; PMC: PMC11011287 WISCi004-BWAi001-AMLUi008-AMLUi009-AMLUi007-HMLUi007-JMLUi010-BMLUi001-MMLUi002-G 2024-03-22 2024-03-22 PubMed: 38612385 DOI: 10.3390/ijms25073575 -
Carvalho S, Santos JI, Moreira L, Duarte AJ, Gaspar P, Rocha H, Encarnação M, Ribeiro D, Barbosa Almeida M, Gonçalves M, David H, Matos L, Amaral O, Diogo L, Ferreira S, Santos C, Martins E, Prata MJ, Pereira de Almeida L, Alves S, Coutinho MF
Modeling Lysosomal Storage Disorders in an Innovative Way: Establishment and Characterization of Stem Cell Lines from Human Exfoliated Deciduous Teeth of Mucopolysaccharidosis Type II Patients
Carvalho S et al. Modeling Lysosomal Storage Disorders in an Innovative Way: Establishment and Characterization of Stem Cell Lines from Human Exfoliated Deciduous Teeth of Mucopolysaccharidosis Type II Patients. . 2024-03-21. Pubmed ID: 38542525; DOI: 10.3390/ijms25063546; PMC: PMC10970756 INSAi002-A 2024-03-21 2024-03-21 PubMed: 38542525 DOI: 10.3390/ijms25063546Associated cell lines:
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Capendale PE, García-Rodríguez I, Ambikan AT, Mulder LA, Depla JA, Freeze E, Koen G, Calitz C, Sood V, Vieira de Sá R, Neogi U, Pajkrt D, Sridhar A, Wolthers KC
Parechovirus infection in human brain organoids: host innate inflammatory response and not neuro-infectivity correlates to neurologic disease
Capendale PE et al. Parechovirus infection in human brain organoids: host innate inflammatory response and not neuro-infectivity correlates to neurologic disease. . 2024-03-21. Pubmed ID: 38514653; DOI: 10.1038/s41467-024-46634-9; PMC: PMC10958052 WISCi004-B 2024-03-21 2024-03-21 PubMed: 38514653 DOI: 10.1038/s41467-024-46634-9Associated cell lines:
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Wang Q, Capelletti S, Liu J, Janssen JM, Gonçalves MAFV
Selection-free precise gene repair using high-capacity adenovector delivery of advanced prime editing systems rescues dystrophin synthesis in DMD muscle cells
Wang Q et al. Selection-free precise gene repair using high-capacity adenovector delivery of advanced prime editing systems rescues dystrophin synthesis in DMD muscle cells. . 2024-03-21. Pubmed ID: 38321963; DOI: 10.1093/nar/gkae057 CENSOi001-B 2024-03-21 2024-03-21 PubMed: 38321963 DOI: 10.1093/nar/gkae057Associated cell lines:
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Mueller LM, Isaacson A, Wilson H, Salowka A, Tay I, Gong M, Elbarbary NS, Raile K, Spagnoli FM
Heterozygous missense variant in GLI2 impairs human endocrine pancreas development
Mueller LM et al. Heterozygous missense variant in GLI2 impairs human endocrine pancreas development. . 2024-03-20. Pubmed ID: 38509065; DOI: 10.1038/s41467-024-46740-8; PMC: PMC10954617 HMGUi001-A 2024-03-20 2024-03-20 PubMed: 38509065 DOI: 10.1038/s41467-024-46740-8Associated cell lines:
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Raghunathan N, Sankaran S, Miteu G.
A comprehensive review of iPS cell line-based disease modelling of the polyglutamine spinocerebellar ataxias 2 and 3: a focus on the research outcomes
Raghunathan N et al. A comprehensive review of iPS cell line-based disease modelling of the polyglutamine spinocerebellar ataxias 2 and 3: a focus on the research outcomes. . 2024-03-19. MUSIi004-ACHOPi002-ACHOPi003-AZZUNEUi002-AZZUi014-ACSUXHi001-AIBCHi002-ACSUXHi005-A 2024-03-19 2024-03-19Associated cell lines:
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Vanslambrouck JM, Neil JA, Rudraraju R, Mah S, Tan KS, Groenewegen E, Forbes TA, Karavendzas K, Elliott DA, Porrello ER, Subbarao K, Little MH
Kidney organoids reveal redundancy in viral entry pathways during ACE2-dependent SARS-CoV-2 infection
Vanslambrouck JM et al. Kidney organoids reveal redundancy in viral entry pathways during ACE2-dependent SARS-CoV-2 infection. . 2024-03-19. Pubmed ID: 38334329; DOI: 10.1128/jvi.01802-23; PMC: PMC10949421 MCRIi010-A 2024-03-19 2024-03-19 PubMed: 38334329 DOI: 10.1128/jvi.01802-23Associated cell lines:
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Mohd Hisam NS, Wong KH
Oxidative Stress in Spinocerebellar Ataxia Type 3 and Its Attenuation by Herbal Remedies in Traditional Chinese Medicine: A Systematic Review
Mohd Hisam NS et al. Oxidative Stress in Spinocerebellar Ataxia Type 3 and Its Attenuation by Herbal Remedies in Traditional Chinese Medicine: A Systematic Review. . 2024-03-19. Pubmed ID: 38539908; DOI: 10.3390/antiox13030375; PMC: PMC10968558 MUSIi004-A 2024-03-19 2024-03-19 PubMed: 38539908 DOI: 10.3390/antiox13030375Associated cell lines:
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Roudaut M, Caillaud A, Souguir Z, Bray L, Girardeau A, Rimbert A, Croyal M, Lambert G, Patitucci M, Delpouve G, Vandenhaute É, Le May C, Maubon N, Cariou B, Si‐Tayeb K.
Human induced pluripotent stem cells‐derived liver organoids grown on a Biomimesys® hyaluronic acid‐based hydroscaffold as a new model for studying human lipoprotein metabolism
Roudaut M et al. Human induced pluripotent stem cells‐derived liver organoids grown on a Biomimesys® hyaluronic acid‐based hydroscaffold as a new model for studying human lipoprotein metabolism. . 2024-03-16. ITXi001-A 2024-03-16 2024-03-16Associated cell lines:
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Kathirgamanathan Abiramee, Nair Akshita
Preventing Atrial Fibrillation in Hypertrophic Cardiomyopathy using Angiotensin-Converting Enzyme (ACE) Inhibitors and Angiotensin Receptor Blockers (ARBs)
Kathirgamanathan Abiramee et al. Preventing Atrial Fibrillation in Hypertrophic Cardiomyopathy using Angiotensin-Converting Enzyme (ACE) Inhibitors and Angiotensin Receptor Blockers (ARBs). . 2024-03-15. DOI: 10.26685/urncst.543 SCVIi001-ASCVIi002-A 2024-03-15 2024-03-15 DOI: 10.26685/urncst.543Associated cell lines:
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Shahriyari M, Rinn M, Hofemeier AD, Babych A, Zimmermann WH, Tiburcy M
Protocol to develop force-generating human skeletal muscle organoids
Shahriyari M et al. Protocol to develop force-generating human skeletal muscle organoids. . 2024-03-15. Pubmed ID: 38133957; DOI: 10.1016/j.xpro.2023.102794; PMC: PMC10776636 RUCDRi002-A 2024-03-15 2024-03-15 PubMed: 38133957 DOI: 10.1016/j.xpro.2023.102794Associated cell lines:
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Zhang J, Peng Y, Fu W, Wang R, Cao J, Li S, Tian X, Li Z, Hua C, Zhai Y, Liu Y, Liu M, Sun J, Li X, Zhao X, Dong J
PLEKHM2 deficiency induces impaired mitochondrial clearance and elevated ROS levels in human iPSC-derived cardiomyocytes
Zhang J et al. PLEKHM2 deficiency induces impaired mitochondrial clearance and elevated ROS levels in human iPSC-derived cardiomyocytes. . 2024-03-15. Pubmed ID: 38490981; DOI: 10.1038/s41420-024-01907-6; PMC: PMC10942999 ZZUNEUi022-A 2024-03-15 2024-03-15 PubMed: 38490981 DOI: 10.1038/s41420-024-01907-6Associated cell lines:
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Gao H, Wang Z, Yang F, Wang X, Wang S, Zhang Q, Liu X, Sun Y, Kong J, Yao J
Graphene-integrated mesh electronics with converged multifunctionality for tracking multimodal excitation-contraction dynamics in cardiac microtissues
Gao H et al. Graphene-integrated mesh electronics with converged multifunctionality for tracking multimodal excitation-contraction dynamics in cardiac microtissues. . 2024-03-14. Pubmed ID: 38485708; DOI: 10.1038/s41467-024-46636-7; PMC: PMC10940632 WAe009-A 2024-03-14 2024-03-14 PubMed: 38485708 DOI: 10.1038/s41467-024-46636-7Associated cell lines:
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Gallego Villarejo L, Gerding WM, Bachmann L, Hardt LHI, Bormann S, Nguyen HP, Müller T
Optical Genome Mapping Reveals Genomic Alterations upon Gene Editing in hiPSCs: Implications for Neural Tissue Differentiation and Brain Organoid Research
Gallego Villarejo L et al. Optical Genome Mapping Reveals Genomic Alterations upon Gene Editing in hiPSCs: Implications for Neural Tissue Differentiation and Brain Organoid Research. . 2024-03-14. Pubmed ID: 38534351; DOI: 10.3390/cells13060507; PMC: PMC10969360 BIONi010-CBIONi010-C-29 2024-03-14 2024-03-14 PubMed: 38534351 DOI: 10.3390/cells13060507Associated cell lines:
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Karakan MÇ, Ewoldt JK, Segarra AJ, Sundaram S, Wang MC, White AE, Chen CS, Ekinci KL
Geometry and length control of 3D engineered heart tissues using direct laser writing
Karakan MÇ et al. Geometry and length control of 3D engineered heart tissues using direct laser writing. . 2024-03-12. Pubmed ID: 38317604; DOI: 10.1039/d3lc00752a; PMC: PMC10929702 SCVIi001-ASCVIi002-A 2024-03-12 2024-03-12 PubMed: 38317604 DOI: 10.1039/d3lc00752aAssociated cell lines:
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Yu Yang, Wang Cankun, Ye Shiqiao, Xu Zhaohui, Lin Hui, Texter Karen, Shukla Vasudha, Ghadiali Samir, Ma Qin, Garg Vidu, Zhao Ming-Tao
Abnormal Progenitor Cell Differentiation and Cardiomyocyte Proliferation in Hypoplastic Right Heart Syndrome
Yu Yang et al. Abnormal Progenitor Cell Differentiation and Cardiomyocyte Proliferation in Hypoplastic Right Heart Syndrome. . 2024-03-12. DOI: 10.1161/circulationaha.123.064213 NCHi003-A 2024-03-12 2024-03-12 DOI: 10.1161/circulationaha.123.064213Associated cell lines:
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Knauer C, Haltern H, Schoger E, Kügler S, Roos L, Zelarayán LC, Hasenfuss G, Zimmermann WH, Wollnik B, Cyganek L
Preclinical evaluation of CRISPR-based therapies for Noonan syndrome caused by deep-intronic LZTR1 variants
Knauer C et al. Preclinical evaluation of CRISPR-based therapies for Noonan syndrome caused by deep-intronic LZTR1 variants. . 2024-03-12. Pubmed ID: 38333672; DOI: 10.1016/j.omtn.2024.102123; PMC: PMC10851011 UMGi030-AUMGi031-AUMGi032-AUMGi033-AUMGi014-CUMGi031-A-1UMGi030-A-1UMGi030-A-2UMGi031-A-2UMGi030-A-3 2024-03-12 2024-03-12 PubMed: 38333672 DOI: 10.1016/j.omtn.2024.102123Associated cell lines:
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Haubenreich C, Lenz M, Schuppert A, Peitz M, Koch P, Zenke M, Brüstle O
Epigenetic and Transcriptional Shifts in Human Neural Stem Cells after Reprogramming into Induced Pluripotent Stem Cells and Subsequent Redifferentiation
Haubenreich C et al. Epigenetic and Transcriptional Shifts in Human Neural Stem Cells after Reprogramming into Induced Pluripotent Stem Cells and Subsequent Redifferentiation. . 2024-03-12. Pubmed ID: 38542188; DOI: 10.3390/ijms25063214; PMC: PMC10969834 WAe009-AWAe009-A-2 2024-03-12 2024-03-12 PubMed: 38542188 DOI: 10.3390/ijms25063214Associated cell lines:
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Amartumur Sarnai, Nguyen Huong, Huynh Thuy, Kim Testaverde S., Woo Ran-Sook, Oh Eungseok, Kim Kyeong Kyu, Lee Luke P., Heo Chaejeong
Neuropathogenesis-on-chips for neurodegenerative diseases
Amartumur Sarnai et al. Neuropathogenesis-on-chips for neurodegenerative diseases. . 2024-03-12. DOI: 10.1038/s41467-024-46554-8 ZZUi007-A 2024-03-12 2024-03-12 DOI: 10.1038/s41467-024-46554-8Associated cell lines:
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Ren Jinfeng, Liu Ke, Hu Lang, Yang Ruoning, Liu Yuting, Wang Siyu, Chen Xinzhu, Zhao Shuli, Jing Luyao, Liu Tiantian, Hu Bin, Zhang Xuefeng, Wang Hui, Li Hui
An Efficient Probe-Based Quantitative PCR Assay Targeting Human-Specific DNA in ST6GALNAC3 for the Quantification of Human Cells in Preclinical Animal Models
Ren Jinfeng et al. An Efficient Probe-Based Quantitative PCR Assay Targeting Human-Specific DNA in ST6GALNAC3 for the Quantification of Human Cells in Preclinical Animal Models. . 2024-03-08. DOI: 10.1007/s12033-024-01115-8 SDUBMSi009-A 2024-03-08 2024-03-08 DOI: 10.1007/s12033-024-01115-8Associated cell lines:
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Gui Le-Kun, Liu Huang-Jun, Jin Li-Jun, Peng Xiao-Chun
Krüpple-like factors in cardiomyopathy: emerging player and therapeutic opportunities
Gui Le-Kun et al. Krüpple-like factors in cardiomyopathy: emerging player and therapeutic opportunities. . 2024-03-07. DOI: 10.3389/fcvm.2024.1342173 USFi004-A 2024-03-07 2024-03-07 DOI: 10.3389/fcvm.2024.1342173Associated cell lines:
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Podleśny-Drabiniok A, Novikova G, Liu Y, Dunst J, Temizer R, Giannarelli C, Marro S, Kreslavsky T, Marcora E, Goate AM
BHLHE40/41 regulate microglia and peripheral macrophage responses associated with Alzheimer's disease and other disorders of lipid-rich tissues
Podleśny-Drabiniok A et al. BHLHE40/41 regulate microglia and peripheral macrophage responses associated with Alzheimer's disease and other disorders of lipid-rich tissues. . 2024-03-06. Pubmed ID: 38448474; DOI: 10.1038/s41467-024-46315-7; PMC: PMC10917780 UCSFi001-A 2024-03-06 2024-03-06 PubMed: 38448474 DOI: 10.1038/s41467-024-46315-7Associated cell lines:
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Alowaysi Maryam, Baadhaim Moayad, Al-Shehri Mohammad, Alzahrani Hajar, Badkok Amani, Attas Hanouf, Zakri Samer, Alameer Seham, Malibari Dalal, Hosawi Manal, Daghestani Mustafa, Al-Ghamdi Khalid, Zia Asima, Tegne Jesper, Alfadhel Majid, Aboalola Doaa, Alsayegh Khaled
Derivation of two iPSC lines (KAIMRCi004-A, KAIMRCi004-B) from a Saudi patient with Biotin-Thiamine-Responsive Basal Ganglia disease (BTBGD) carrying homozygous pathogenic missense variant in the SCL19A3 gene
Alowaysi Maryam et al. Derivation of two iPSC lines (KAIMRCi004-A, KAIMRCi004-B) from a Saudi patient with Biotin-Thiamine-Responsive Basal Ganglia disease (BTBGD) carrying homozygous pathogenic missense variant in the SCL19A3 gene. . 2024-03-06. DOI: 10.21203/rs.3.rs-3977137/v1 KAIMRCi004-AKAIMRCi004-B 2024-03-06 2024-03-06 DOI: 10.21203/rs.3.rs-3977137/v1Associated cell lines:
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Shi De-Li
RNA-Binding Proteins in Cardiomyopathies
Shi De-Li. RNA-Binding Proteins in Cardiomyopathies. . 2024-03-05. DOI: 10.3390/jcdd11030088 UMGi255-A 2024-03-05 2024-03-05 DOI: 10.3390/jcdd11030088Associated cell lines:
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Du X, Kong D, Guo R, Liu B, He J, Zhang J, Amponsah AE, Cui H, Ma J
Combined transplantation of hiPSC-NSC and hMSC ameliorated neuroinflammation and promoted neuroregeneration in acute spinal cord injury
Du X et al. Combined transplantation of hiPSC-NSC and hMSC ameliorated neuroinflammation and promoted neuroregeneration in acute spinal cord injury. . 2024-03-05. Pubmed ID: 38444003; DOI: 10.1186/s13287-024-03655-x; PMC: PMC10916262 HEBHMUi002-A 2024-03-05 2024-03-05 PubMed: 38444003 DOI: 10.1186/s13287-024-03655-xAssociated cell lines:
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Bryl Rut, Kulus Magdalena, Bryja Artur, Domagała Dominika, Mozdziak Paul, Antosik Paweł, Bukowska Dorota, Zabel Maciej, Dzięgiel Piotr, Kempisty Bartosz
Cardiac progenitor cell therapy: mechanisms of action
Bryl Rut et al. Cardiac progenitor cell therapy: mechanisms of action. . 2024-03-05. DOI: 10.1186/s13578-024-01211-x GIBHi002-AGIBHi002-A-2 2024-03-05 2024-03-05 DOI: 10.1186/s13578-024-01211-xAssociated cell lines:
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Heider Johanna, Stahl Aaron, Sperlich Denise, Hartmann Sophia-Marie, Vogel Sabrina, Breitmeyer Ricarda, Templin Markus, Volkmer Hansjürgen
Defined co-cultures of glutamatergic and GABAergic neurons with a mutation in DISC1 reveal aberrant phenotypes in GABAergic neurons
Heider Johanna et al. Defined co-cultures of glutamatergic and GABAergic neurons with a mutation in DISC1 reveal aberrant phenotypes in GABAergic neurons. . 2024-03-04. DOI: 10.1186/s12868-024-00858-z TMOi001-ATMOi001-A-5TMOi001-A-6 2024-03-04 2024-03-04 DOI: 10.1186/s12868-024-00858-zAssociated cell lines:
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King NE, Courtney JM, Brown LS, Fortune AJ, Blackburn NB, Fletcher JL, Cashion JM, Talbot J, Pébay A, Hewitt AW, Morris GP, Young KM, Cook AL, Sutherland BA
Induced pluripotent stem cell derived pericytes respond to mediators of proliferation and contractility
King NE et al. Induced pluripotent stem cell derived pericytes respond to mediators of proliferation and contractility. . 2024-03-03. Pubmed ID: 38433209; DOI: 10.1186/s13287-024-03671-x; PMC: PMC10910734 MNZTASi001-AMNZTASi019-AMNZTASi021-AMNZTASi022-A 2024-03-03 2024-03-03 PubMed: 38433209 DOI: 10.1186/s13287-024-03671-xAssociated cell lines:
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Thongsa-Ad U, Wongpan A, Wongkummool W, Chaiwijit P, Uppakara K, Chaiyakitpattana G, Singpant P, Tong-Ngam P, Chukhan A, Pabuprappap W, Wongniam S, Suksamrarn A, Hongeng S, Anurathapan U, Kulkeaw K, Tubsuwan A, Bhukhai K
Improving hematopoietic differentiation from human induced pluripotent stem cells by the modulation of Hippo signaling with a diarylheptanoid derivative
Thongsa-Ad U et al. Improving hematopoietic differentiation from human induced pluripotent stem cells by the modulation of Hippo signaling with a diarylheptanoid derivative. . 2024-03-03. Pubmed ID: 38433217; DOI: 10.1186/s13287-024-03686-4; PMC: PMC10910864 MUi019-A 2024-03-03 2024-03-03 PubMed: 38433217 DOI: 10.1186/s13287-024-03686-4Associated cell lines:
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Klein Thomas, Grüner Julia, Breyer Maximilian, Schlegel Jan, Schottmann Nicole Michelle, Hofmann Lukas, Gauss Kevin, Mease Rebecca, Erbacher Christoph, Finke Laura, Klein Alexandra, Klug Katharina, Karl-Schöller Franziska, Vignolo Bettina, Reinhard Sebastian, Schneider Tamara, Günther Katharina, Fink Julian, Dudek Jan, Maack Christoph, Klopocki Eva, Seibel Jürgen, Edenhofer Frank, Wischmeyer Erhard, Sauer Markus, Üçeyler Nurcan
Small fibre neuropathy in Fabry disease: a human-derived neuronal in vitro disease model and pilot data
Klein Thomas et al. Small fibre neuropathy in Fabry disease: a human-derived neuronal in vitro disease model and pilot data. . 2024-03-01. DOI: 10.1093/braincomms/fcae095 UKWNLi002-A 2024-03-01 2024-03-01 DOI: 10.1093/braincomms/fcae095Associated cell lines:
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Schreiber MK, Zafeiriou MP
Generation of a fluorescent oligodendrocyte reporter line in human induced pluripotent stem cells
Schreiber MK et al. Generation of a fluorescent oligodendrocyte reporter line in human induced pluripotent stem cells. . 2024-03-00. Pubmed ID: 38219302; DOI: 10.1016/j.scr.2023.103295 RUCDRi002-A-70 2024-03-00 2024-03-00 PubMed: 38219302 DOI: 10.1016/j.scr.2023.103295Associated cell lines:
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Yuan He-Ling, Chang Le, Fan Wei-Wen, Liu Xin, Li Qiang, Tian Chuan, Zhao Jing, Li Zi-An, Pan Xing-Hua, Zhu Xiang-Qing
Application and challenges of stem cells in cardiovascular aging
Yuan He-Ling et al. Application and challenges of stem cells in cardiovascular aging. . 2024-03-00. DOI: 10.1016/j.reth.2023.11.009 UALGi001-A 2024-03-00 2024-03-00 DOI: 10.1016/j.reth.2023.11.009Associated cell lines:
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Alowaysi M, Al-Shehri M, Badkok A, Attas H, Aboalola D, Baadhaim M, Alzahrani H, Daghestani M, Zia A, Al-Ghamdi K, Al-Ghamdi A, Zakri S, Aouabdi S, Tegner J, Alsayegh K
Generation of iPSC lines (KAIMRCi003A, KAIMRCi003B) from a Saudi patient with Dravet syndrome carrying homozygous mutation in the CPLX1 gene and heterozygous mutation in SCN9A
Alowaysi M et al. Generation of iPSC lines (KAIMRCi003A, KAIMRCi003B) from a Saudi patient with Dravet syndrome carrying homozygous mutation in the CPLX1 gene and heterozygous mutation in SCN9A. . 2024-03-00. Pubmed ID: 38110787; DOI: 10.1007/s13577-023-01016-z; PMC: PMC10890977 KAIMRCi001-AKAIMRCi003-AKAIMRCi003-B 2024-03-00 2024-03-00 PubMed: 38110787 DOI: 10.1007/s13577-023-01016-zAssociated cell lines:
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Mora-Roldan GA, Nava J, Gazarian K, Zenteno JC
Generation of the induced pluripotent stem cell line IOCVi001-A from a patient with the MFRP-related retinitis pigmentosa-nanophthalmos syndrome
Mora-Roldan GA et al. Generation of the induced pluripotent stem cell line IOCVi001-A from a patient with the MFRP-related retinitis pigmentosa-nanophthalmos syndrome. . 2024-03-00. Pubmed ID: 38217995; DOI: 10.1016/j.scr.2024.103309 IOCVi001-A 2024-03-00 2024-03-00 PubMed: 38217995 DOI: 10.1016/j.scr.2024.103309Associated cell lines:
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Tripathi D, Manhas A, Noishiki C, Wu D, Adkar S, Sallam K, Fukaya E, Leeper NJ, Sayed N
Generation of induced pluripotent stem cell line from a patient suffering from arterial calcification due to deficiency of CD73 (ACDC)
Tripathi D et al. Generation of induced pluripotent stem cell line from a patient suffering from arterial calcification due to deficiency of CD73 (ACDC). . 2024-03-00. Pubmed ID: 38199067; DOI: 10.1016/j.scr.2023.103285; PMC: PMC11164231 BFVSBi001-A 2024-03-00 2024-03-00 PubMed: 38199067 DOI: 10.1016/j.scr.2023.103285Associated cell lines:
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Houweling PJ, Crossman V, Tiong CF, Coles CA, Taylor RL, Clayton JS, Graham A, Vlahos K, Howden SE, North KN
Generation of a human ACTA1-tdTomato reporter iPSC line using CRISPR/Cas9 editing
Houweling PJ et al. Generation of a human ACTA1-tdTomato reporter iPSC line using CRISPR/Cas9 editing. . 2024-03-00. Pubmed ID: 38277710; DOI: 10.1016/j.scr.2024.103313 MCRIi001-AMCRIi001-A-2MCRIi010-A-1 2024-03-00 2024-03-00 PubMed: 38277710 DOI: 10.1016/j.scr.2024.103313Associated cell lines:
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Breyer Maximilian, Grüner Julia, Klein Alexandra, Finke Laura, Klug Katharina, Sauer Markus, Üçeyler Nurcan
In vitro characterization of cells derived from a patient with the GLA variant c.376A>G (p.S126G) highlights a non-pathogenic role in Fabry disease
Breyer Maximilian et al. In vitro characterization of cells derived from a patient with the GLA variant c.376A>G (p.S126G) highlights a non-pathogenic role in Fabry disease. . 2024-03-00. DOI: 10.1016/j.ymgmr.2023.101029 UKWNLi005-A 2024-03-00 2024-03-00 DOI: 10.1016/j.ymgmr.2023.101029Associated cell lines:
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Ropret S, Khurana P, Fabčič T, Cvetkovska J, Trobec A, Jokhadar ŠZ, Ilic D, McGrath JA, Guttmann-Gruber C, Liovic M
Induced pluripotent stem cell (iPSC) line MLi005-A derived from a patient with dominant dystrophic epidermolysis bullosa (DDEB)
Ropret S et al. Induced pluripotent stem cell (iPSC) line MLi005-A derived from a patient with dominant dystrophic epidermolysis bullosa (DDEB). . 2024-03-00. Pubmed ID: 38271763; DOI: 10.1016/j.scr.2024.103306 KCLi003-AMLi005-A 2024-03-00 2024-03-00 PubMed: 38271763 DOI: 10.1016/j.scr.2024.103306 -
Tiwari Vikas, Alam Md Jahangir, Bhatia Madhavi, Navya Malladi, Banerjee Sanjay K.
The structure and function of lamin A/C: Special focus on cardiomyopathy and therapeutic interventions
Tiwari Vikas et al. The structure and function of lamin A/C: Special focus on cardiomyopathy and therapeutic interventions. . 2024-03-00. DOI: 10.1016/j.lfs.2024.122489 EURACi015-A 2024-03-00 2024-03-00 DOI: 10.1016/j.lfs.2024.122489Associated cell lines:
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Höpperger S, Spathopoulou A, Mayer-Suess L, Suarez-Cubero M, Sillaber K, Spreiz A, Kiechl S, Edenhofer F, Fellner L
Generation of the human induced pluripotent stem cell line (IBKMOLi003-A) from PBMCs of a vascular Ehlers-Danlos syndrome (vEDS) patient carrying the heterozygous nonsense mutation c.430C > T (p.Q105*) in the COL3A1 gene
Höpperger S et al. Generation of the human induced pluripotent stem cell line (IBKMOLi003-A) from PBMCs of a vascular Ehlers-Danlos syndrome (vEDS) patient carrying the heterozygous nonsense mutation c.430C > T (p.Q105*) in the COL3A1 gene. . 2024-03-00. Pubmed ID: 38301384; DOI: 10.1016/j.scr.2024.103321 IBKMOLi003-A 2024-03-00 2024-03-00 PubMed: 38301384 DOI: 10.1016/j.scr.2024.103321Associated cell lines:
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Djemai M, Jauvin D, Poulin H, Chapotte-Baldacci CA, Chahine M
Generation of a patient-specific iPSC cell line with cardiac arrhythmias and dilated cardiomyopathy (CBRCULi016-A), an isogenic control (CBRCULi016-A-1), and a paternal control (CBRCULi017-A)
Djemai M et al. Generation of a patient-specific iPSC cell line with cardiac arrhythmias and dilated cardiomyopathy (CBRCULi016-A), an isogenic control (CBRCULi016-A-1), and a paternal control (CBRCULi017-A). . 2024-03-00. Pubmed ID: 38232626; DOI: 10.1016/j.scr.2024.103308 CBRCULi016-ACBRCULi017-ACBRCULi016-A-1 2024-03-00 2024-03-00 PubMed: 38232626 DOI: 10.1016/j.scr.2024.103308Associated cell lines:
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Binder S, Ramachandran H, Hildebrandt B, Dobner J, Rossi A
Prime-Editing of human ACTB in induced pluripotent stem cells to model human ACTB Loss-of-Function diseases and compensatory mechanisms
Binder S et al. Prime-Editing of human ACTB in induced pluripotent stem cells to model human ACTB Loss-of-Function diseases and compensatory mechanisms. . 2024-03-00. Pubmed ID: 38217996; DOI: 10.1016/j.scr.2024.103304 IUFi004-AIUFi004-A-1IUFi004-A-2 2024-03-00 2024-03-00 PubMed: 38217996 DOI: 10.1016/j.scr.2024.103304Associated cell lines:
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Sun Hao, He Zhazheng, Gao Yao, Yang Yanhan, Wang Yachang, Gu Aihua, Xu Jin, Quan Yingyi, Yang Yang
Polyoxyethylene tallow amine and glyphosate exert different developmental toxicities on human pluripotent stem cells-derived heart organoid model
Sun Hao et al. Polyoxyethylene tallow amine and glyphosate exert different developmental toxicities on human pluripotent stem cells-derived heart organoid model. . 2024-03-00. DOI: 10.1016/j.scitotenv.2024.170675 WAe009-A-H 2024-03-00 2024-03-00 DOI: 10.1016/j.scitotenv.2024.170675Associated cell lines:
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Huang J, Jiang Q, Pang D, Yu Y, Cui Y, Li C, Shang H
Generation of induced pluripotent stem cell line LNDWCHi001-A from a patient with early-onset Parkinson's disease carrying the homozygous c.1898C > T (p. A633V) mutation in the PLA2G6 gene
Huang J et al. Generation of induced pluripotent stem cell line LNDWCHi001-A from a patient with early-onset Parkinson's disease carrying the homozygous c.1898C > T (p. A633V) mutation in the PLA2G6 gene. . 2024-03-00. Pubmed ID: 38215561; DOI: 10.1016/j.scr.2024.103305 LNDWCHi001-A 2024-03-00 2024-03-00 PubMed: 38215561 DOI: 10.1016/j.scr.2024.103305Associated cell lines:
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Miellet S, St Clair-Glover M, Maddock M, Dottori M
Generation of a gene-edited H9 embryonic stem cell line carrying a DOX-inducible NGN2 expression cassette in the CLYBL locus
Miellet S et al. Generation of a gene-edited H9 embryonic stem cell line carrying a DOX-inducible NGN2 expression cassette in the CLYBL locus. . 2024-03-00. Pubmed ID: 38244534; DOI: 10.1016/j.scr.2024.103312 WAe009-A-W 2024-03-00 2024-03-00 PubMed: 38244534 DOI: 10.1016/j.scr.2024.103312Associated cell lines:
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Schulze-Bahr E.
Kardiogenetik in Deutschland – ein (Rück‑)Blick
Schulze-Bahr E.. Kardiogenetik in Deutschland – ein (Rück‑)Blick. . 2024-03-00. DOI: 10.1007/s00399-024-01008-y UKMi005-A 2024-03-00 2024-03-00 DOI: 10.1007/s00399-024-01008-yAssociated cell lines:
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Maddhesiya Jyoti, Mohapatra Bhagyalaxmi
Understanding the Genetic and Non-genetic Interconnections in the Aetiology of Isolated Congenital Heart Disease: An Updated Review: Part 1
Maddhesiya Jyoti et al. Understanding the Genetic and Non-genetic Interconnections in the Aetiology of Isolated Congenital Heart Disease: An Updated Review: Part 1. . 2024-03-00. DOI: 10.1007/s11886-024-02022-9 YAHKMUi001-A 2024-03-00 2024-03-00 DOI: 10.1007/s11886-024-02022-9Associated cell lines:
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Jung M, Jung JS, Pfeifer J, Hartmann C, Ehrhardt T, Abid CL, Kintzel J, Puls A, Navarrete Santos A, Hollemann T, Riemann D, Rujescu D
Neuronal Stem Cells from Late-Onset Alzheimer Patients Show Altered Regulation of Sirtuin 1 Depending on Apolipoprotein E Indicating Disturbed Stem Cell Plasticity
Jung M et al. Neuronal Stem Cells from Late-Onset Alzheimer Patients Show Altered Regulation of Sirtuin 1 Depending on Apolipoprotein E Indicating Disturbed Stem Cell Plasticity. . 2024-03-00. Pubmed ID: 37728850; DOI: 10.1007/s12035-023-03633-z; PMC: PMC10896791 WISCi004-BWAi001-BMLUi008-AMLUi009-AMLUi007-HMLUi007-JMLUi008-BMLUi010-B 2024-03-00 2024-03-00 PubMed: 37728850 DOI: 10.1007/s12035-023-03633-z -
Benedetti Maria Cristina, D'andrea Tiziano, Colantoni Alessio, Silachev Denis, de Turris Valeria, Boussadia Zaira, Babenko Valentina A., Volovikov Egor A., Belikova Lilia, Bogomazova Alexandra N., Pepponi Rita, Whye Dosh, Buttermore Elizabeth D., Tartaglia Gian Gaetano, Lagarkova Maria A., Katanaev Vladimir L., Musayev Ilya, Martinelli Simone, Fucile Sergio, Rosa Alessandro
Cortical neurons obtained from patient-derived iPSCs with GNAO1 p.G203R variant show altered differentiation and functional properties
Benedetti Maria Cristina et al. Cortical neurons obtained from patient-derived iPSCs with GNAO1 p.G203R variant show altered differentiation and functional properties. . 2024-03-00. DOI: 10.1016/j.heliyon.2024.e26656 RCPCMi004-A 2024-03-00 2024-03-00 DOI: 10.1016/j.heliyon.2024.e26656Associated cell lines:
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Saleh Mahmood Ali, Amer-Sarsour Fatima, Berant Asaf, Pasmanik-Chor Metsada, Kobo Hila, Sharabi Yehonatan, Vatine Gad D., Ashkenazi Avraham
Chronic and acute exposure to rotenone reveals distinct Parkinson's disease-related phenotypes in human iPSC-derived peripheral neurons
Saleh Mahmood Ali et al. Chronic and acute exposure to rotenone reveals distinct Parkinson's disease-related phenotypes in human iPSC-derived peripheral neurons. . 2024-03-00. DOI: 10.1016/j.freeradbiomed.2024.01.016 BGUi004-ABGUi005-A 2024-03-00 2024-03-00 DOI: 10.1016/j.freeradbiomed.2024.01.016 -
Zabalegui F, Castañeda SL, Amin G, Belli C, Miriuka SG, Moro LN
Derivation of two human induced pluripotent stem cell lines carrying a missense mutation in FHL1 (c.377G > A, p.C126Y) linked to familial muscular dystrophy
Zabalegui F et al. Derivation of two human induced pluripotent stem cell lines carrying a missense mutation in FHL1 (c.377G > A, p.C126Y) linked to familial muscular dystrophy. . 2024-03-00. Pubmed ID: 38244535; DOI: 10.1016/j.scr.2024.103307 INEUi003-AINEUi004-A 2024-03-00 2024-03-00 PubMed: 38244535 DOI: 10.1016/j.scr.2024.103307Associated cell lines:
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Jinliang D, Fang B, Xiaofeng Z, Xiaoshun H, Anbin H
Generation of a human induced pluripotent stem cell line overexpressing CCL22 with islet cells differentiation potential
Jinliang D et al. Generation of a human induced pluripotent stem cell line overexpressing CCL22 with islet cells differentiation potential. . 2024-03-00. Pubmed ID: 38217994; DOI: 10.1016/j.scr.2023.103302 CNNDi001-ACNNDi001-A-2 2024-03-00 2024-03-00 PubMed: 38217994 DOI: 10.1016/j.scr.2023.103302Associated cell lines:
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Wang YB, Lv YF, Zhang Y, Wang W
Generation of the human induced pluripotent stem cell line PUMCi005-A from a patient with Perrault syndrome
Wang YB et al. Generation of the human induced pluripotent stem cell line PUMCi005-A from a patient with Perrault syndrome. . 2024-03-00. Pubmed ID: 38295749; DOI: 10.1016/j.scr.2024.103318 PUMCi002-APUMCi005-A 2024-03-00 2024-03-00 PubMed: 38295749 DOI: 10.1016/j.scr.2024.103318Associated cell lines:
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Han HW, Im YS, Kim YO, Kwak S, Cho SJ
Generation of a CAG-EGFP tagged cell line (KSCBi017-A-2) from human induced pluripotent stem cells using CRISPR/Cas9
Han HW et al. Generation of a CAG-EGFP tagged cell line (KSCBi017-A-2) from human induced pluripotent stem cells using CRISPR/Cas9. . 2024-03-00. Pubmed ID: 38211411; DOI: 10.1016/j.scr.2024.103303 KSCBi005-AKSCBi005-A-5KSCBi017-AKSCBi017-A-2 2024-03-00 2024-03-00 PubMed: 38211411 DOI: 10.1016/j.scr.2024.103303Associated cell lines:
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Liu H, Zhao Z, Zhao J, Xu L, Li J, Zhang B
Derivation of induced pluripotent stem cell SHEHDNi002-A from a 68-year-old Chinese Han Parkinson's disease patient carrying LRRK2 and DNAJC6 mutations
Liu H et al. Derivation of induced pluripotent stem cell SHEHDNi002-A from a 68-year-old Chinese Han Parkinson's disease patient carrying LRRK2 and DNAJC6 mutations. . 2024-03-00. Pubmed ID: 38219303; DOI: 10.1016/j.scr.2023.103297 SHEHDNi002-A 2024-03-00 2024-03-00 PubMed: 38219303 DOI: 10.1016/j.scr.2023.103297Associated cell lines:
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Alsalloum A, Asaad W, Krupinova J, Kegeles E, Sirotkina P, Panova A, Mityaeva O, Volchkov P
Generation of induced pluripotent stem cell line (MIPTi002-A) derived from a patient with a heterozygous type mutation in the CDC73 gene
Alsalloum A et al. Generation of induced pluripotent stem cell line (MIPTi002-A) derived from a patient with a heterozygous type mutation in the CDC73 gene. . 2024-03-00. Pubmed ID: 38237426; DOI: 10.1016/j.scr.2024.103311 MIPTi002-A 2024-03-00 2024-03-00 PubMed: 38237426 DOI: 10.1016/j.scr.2024.103311Associated cell lines:
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Milosic Filip, Hengstschläger Markus, Osmanagic-Myers Selma
Premature aging in genetic diseases: what conclusions can be drawn for physiological aging
Milosic Filip et al. Premature aging in genetic diseases: what conclusions can be drawn for physiological aging. . 2024-02-28. DOI: 10.3389/fragi.2023.1327833 REGUi003-A 2024-02-28 2024-02-28 DOI: 10.3389/fragi.2023.1327833Associated cell lines:
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Yoon Da Eun, Lee Hyunji, Kim Kyoungmi
Recent Research Trends in Stem Cells Using CRISPR/Cas-Based Genome Editing Methods
Yoon Da Eun et al. Recent Research Trends in Stem Cells Using CRISPR/Cas-Based Genome Editing Methods. . 2024-02-28. DOI: 10.15283/ijsc23030 WAe001-AWAe001-A-20 2024-02-28 2024-02-28 DOI: 10.15283/ijsc23030Associated cell lines:
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Arribas-Carreira Laura, Castro Margarita, García Fernando, Navarrete Rosa, Bravo-Alonso Irene, Zafra Francisco, Ugarte Magdalena, Richard Eva, Pérez Belén, Rodríguez-Pombo Pilar
Metabolic Rewiring and Altered Glial Differentiation in an iPSC-Derived Astrocyte Model Derived from a Nonketotic Hyperglycinemia Patient
Arribas-Carreira Laura et al. Metabolic Rewiring and Altered Glial Differentiation in an iPSC-Derived Astrocyte Model Derived from a Nonketotic Hyperglycinemia Patient. . 2024-02-28. DOI: 10.3390/ijms25052814 UAMi005-A 2024-02-28 2024-02-28 DOI: 10.3390/ijms25052814Associated cell lines:
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Gupta Pragya, Goswami Sangam Giri, Kumari Geeta, Saravanakumar Vinodh, Bhargava Nupur, Rai Akhila Balakrishna, Singh Praveen, Bhoyar Rahul C., Arvinden V. R., Gunda Padma, Jain Suman, Narayana Vanya Kadla, Deolankar Sayali C., Prasad T. S. Keshava, Natarajan Vivek T., Scaria Vinod, Singh Shailja, Ramalingam Sivaprakash
Development of pathophysiologically relevant models of sickle cell disease and β-thalassemia for therapeutic studies
Gupta Pragya et al. Development of pathophysiologically relevant models of sickle cell disease and β-thalassemia for therapeutic studies. . 2024-02-27. DOI: 10.1038/s41467-024-46036-x IGIBi001-AIGIBi002-A 2024-02-27 2024-02-27 DOI: 10.1038/s41467-024-46036-xAssociated cell lines:
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Damiani Devid, Baggiani Matteo, Della Vecchia Stefania, Naef Valentina, Santorelli Filippo Maria
Pluripotent Stem Cells as a Preclinical Cellular Model for Studying Hereditary Spastic Paraplegias
Damiani Devid et al. Pluripotent Stem Cells as a Preclinical Cellular Model for Studying Hereditary Spastic Paraplegias. . 2024-02-23. DOI: 10.3390/ijms25052615 FJMUi001-ASDUBMSi001-AHIHRSi003-AHIHRSi003-A-1ZZUi033-A 2024-02-23 2024-02-23 DOI: 10.3390/ijms25052615Associated cell lines:
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Zhou Tianmin, Liu Keyu, Wei Hao, Zhong Qingmei, Luo Daya, Yang Wenjuan, Zhang Ping, Xiao Yingqun
Histopathology and molecular pathology confirmed a diagnosis of atypical Caroli’s syndrome: a case report
Zhou Tianmin et al. Histopathology and molecular pathology confirmed a diagnosis of atypical Caroli’s syndrome: a case report. . 2024-02-22. DOI: 10.1186/s13000-024-01462-9 DHMCi006-A 2024-02-22 2024-02-22 DOI: 10.1186/s13000-024-01462-9Associated cell lines:
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McMahon E, El-Sayed S, Green J, Hoyle C, FitzPatrick L, Jones EV, Corrie E, Kelly RL, Challinor M, Freeman S, Bryce RA, Lawrence CB, Brough D, Kasher PR
Brazilin is a natural product inhibitor of the NLRP3 inflammasome
McMahon E et al. Brazilin is a natural product inhibitor of the NLRP3 inflammasome. . 2024-02-16. Pubmed ID: 38327788; DOI: 10.1016/j.isci.2024.108968; PMC: PMC10847679 WTSIi018-BWTSIi018-B-1 2024-02-16 2024-02-16 PubMed: 38327788 DOI: 10.1016/j.isci.2024.108968Associated cell lines:
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Warin J, Vedrenne N, Tam V, Zhu M, Yin D, Lin X, Guidoux-D'halluin B, Humeau A, Roseiro L, Paillat L, Chédeville C, Chariau C, Riemers F, Templin M, Guicheux J, Tryfonidou MA, Ho JWK, David L, Chan D, Camus A
In vitro and in vivo models define a molecular signature reference for human embryonic notochordal cells
Warin J et al. In vitro and in vivo models define a molecular signature reference for human embryonic notochordal cells. . 2024-02-16. Pubmed ID: 38357665; DOI: 10.1016/j.isci.2024.109018; PMC: PMC10865399 REGUi016-DLIMFRi001-A 2024-02-16 2024-02-16 PubMed: 38357665 DOI: 10.1016/j.isci.2024.109018Associated cell lines:
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Jäntti H, Jonk S, Gómez Budia M, Ohtonen S, Fagerlund I, Fazaludeen MF, Aakko-Saksa P, Pebay A, Lehtonen Š, Koistinaho J, Kanninen KM, Jalava PI, Malm T, Korhonen P
Particulate matter from car exhaust alters function of human iPSC-derived microglia
Jäntti H et al. Particulate matter from car exhaust alters function of human iPSC-derived microglia. . 2024-02-15. Pubmed ID: 38360668; DOI: 10.1186/s12989-024-00564-y; PMC: PMC10870637 BIONi010-CBIONi010-C-2 2024-02-15 2024-02-15 PubMed: 38360668 DOI: 10.1186/s12989-024-00564-yAssociated cell lines:
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Busquets O, Li H, Mohieddin Syed K, Jerez PA, Dunnack J, Bu RL, Verma Y, Pangilinan GR, Martin A, Straub J, Du Y, Simon VM, Poser S, Bush Z, Diaz J, Sahagun A, Gao J, Hernandez DG, Levine KS, Booth EO, Bateup HS, Rio DC, Hockemeyer D, Blauwendraat C, Soldner F
iSCORE-PD: an isogenic stem cell collection to research Parkinson's Disease
Busquets O et al. iSCORE-PD: an isogenic stem cell collection to research Parkinson's Disease. . 2024-02-13. Pubmed ID: 38405931; DOI: 10.1101/2024.02.12.579917; PMC: PMC10888955 WIBRe001-AWIBRe001-A-4WIBRe001-A-5WIBRe001-A-6WIBRe001-A-7WIBRe001-A-8WIBRe001-A-10WIBRe001-A-11WIBRe001-A-12WIBRe001-A-13WIBRe001-A-15WIBRe001-A-16WIBRe001-A-17WIBRe001-A-18WIBRe001-A-19WIBRe001-A-20WIBRe001-A-21WIBRe001-A-22WIBRe001-A-23WIBRe001-A-24WIBRe001-A-25WIBRe001-A-26WIBRe001-A-27WIBRe001-A-28WIBRe001-A-29WIBRe001-A-30WIBRe001-A-31WIBRe001-A-32WIBRe001-A-33WIBRe001-A-34WIBRe001-A-35WIBRe001-A-36WIBRe001-A-37WIBRe001-A-38WIBRe001-A-39WIBRe001-A-40WIBRe001-A-41WIBRe001-A-42WIBRe001-A-43WIBRe001-A-44WIBRe001-A-45WIBRe001-A-46WIBRe001-A-47WIBRe001-A-48WIBRe001-A-49WIBRe001-A-50WIBRe001-A-51WIBRe001-A-52WIBRe001-A-53WIBRe001-A-54WIBRe001-A-55WIBRe001-A-56WIBRe001-A-57WIBRe001-A-58WIBRe001-A-59WIBRe001-A-60WIBRe001-A-61WIBRe001-A-62WIBRe001-A-63WIBRe001-A-64WIBRe001-A-65WIBRe001-A-66WIBRe001-A-67WIBRe001-A-68WIBRe001-A-69WIBRe001-A-70WIBRe001-A-71WIBRe001-A-72WIBRe001-A-73 2024-02-13 2024-02-13 PubMed: 38405931 DOI: 10.1101/2024.02.12.579917 -
Hall Duane D., Takeshima Hiroshi, Song Long-Sheng
Structure, Function, and Regulation of the Junctophilin Family
Hall Duane D. et al. Structure, Function, and Regulation of the Junctophilin Family. . 2024-02-12. DOI: 10.1146/annurev-physiol-042022-014926 WAe009-AWAe009-A-36 2024-02-12 2024-02-12 DOI: 10.1146/annurev-physiol-042022-014926Associated cell lines:
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Juul-Madsen K, Parbo P, Ismail R, Ovesen PL, Schmidt V, Madsen LS, Thyrsted J, Gierl S, Breum M, Larsen A, Andersen MN, Romero-Ramos M, Holm CK, Andersen GR, Zhao H, Schuck P, Nygaard JV, Sutherland DS, Eskildsen SF, Willnow TE, Brooks DJ, Vorup-Jensen T
Amyloid-β aggregates activate peripheral monocytes in mild cognitive impairment
Juul-Madsen K et al. Amyloid-β aggregates activate peripheral monocytes in mild cognitive impairment. . 2024-02-09. Pubmed ID: 38336934; DOI: 10.1038/s41467-024-45627-y; PMC: PMC10858199 HMGUi001-A 2024-02-09 2024-02-09 PubMed: 38336934 DOI: 10.1038/s41467-024-45627-yAssociated cell lines:
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Ma Y, Liu X, Zhou M, Sun W, Jiang B, Liu Q, Wang M, Zou Y, Liu Q, Gong Y, Sun G
CUL4B mutations impair human cortical neurogenesis through PP2A-dependent inhibition of AKT and ERK
Ma Y et al. CUL4B mutations impair human cortical neurogenesis through PP2A-dependent inhibition of AKT and ERK. . 2024-02-08. Pubmed ID: 38331954; DOI: 10.1038/s41419-024-06501-3; PMC: PMC10853546 SDQLCHi015-ASDUBMSi002-A 2024-02-08 2024-02-08 PubMed: 38331954 DOI: 10.1038/s41419-024-06501-3Associated cell lines:
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Edzeamey Fred Jonathan, Ramchunder Zenouska, Pourzand Charareh, Anjomani Virmouni Sara
Emerging antioxidant therapies in Friedreich’s ataxia
Edzeamey Fred Jonathan et al. Emerging antioxidant therapies in Friedreich’s ataxia. . 2024-02-06. DOI: 10.3389/fphar.2024.1359618 USFi001-A 2024-02-06 2024-02-06 DOI: 10.3389/fphar.2024.1359618Associated cell lines:
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Norton Benjamin, Quirk Analia, Matsuoka Akihiro J.
Unraveling the Mechanisms of Vestibular Neuron Formation from Human Induced Pluripotent Stem Cells
Norton Benjamin et al. Unraveling the Mechanisms of Vestibular Neuron Formation from Human Induced Pluripotent Stem Cells. . 2024-02-01. DOI: 10.1089/ten.tea.2023.0166 SCTi003-A 2024-02-01 2024-02-01 DOI: 10.1089/ten.tea.2023.0166Associated cell lines:
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Mancini FE, Humphreys PEA, Woods S, Bates N, Cuvertino S, O'Flaherty J, Biant L, Domingos MAN, Kimber SJ
Effect of a retinoic acid analogue on BMP-driven pluripotent stem cell chondrogenesis
Mancini FE et al. Effect of a retinoic acid analogue on BMP-driven pluripotent stem cell chondrogenesis. . 2024-02-01. Pubmed ID: 38302538; DOI: 10.1038/s41598-024-52362-3; PMC: PMC10834951 UMANe002-A 2024-02-01 2024-02-01 PubMed: 38302538 DOI: 10.1038/s41598-024-52362-3Associated cell lines:
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Nappi Francesco
In-Depth Genomic Analysis: The New Challenge in Congenital Heart Disease
Nappi Francesco. In-Depth Genomic Analysis: The New Challenge in Congenital Heart Disease. . 2024-02-01. DOI: 10.3390/ijms25031734 TRNDi032-A 2024-02-01 2024-02-01 DOI: 10.3390/ijms25031734Associated cell lines:
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Sbrini G, Tomasoni Z, Cutrì MR, Pilotta A, Mingotti C, Badolato R, La Via L, Barbon A, Bono F, Fiorentini C
Generation of human induced pluripotent stem cell lines derived from three Noonan syndrome patients from a single family carrying the heterozygous PTPN11 c.188 A > G (p.Y63C) mutation
Sbrini G et al. Generation of human induced pluripotent stem cell lines derived from three Noonan syndrome patients from a single family carrying the heterozygous PTPN11 c.188 A > G (p.Y63C) mutation. . 2024-02-00. Pubmed ID: 38160629; DOI: 10.1016/j.scr.2023.103293 UNIBSi018-AUNIBSi018-BUNIBSi019-AUNIBSi019-BUNIBSi020-AUNIBSi020-B 2024-02-00 2024-02-00 PubMed: 38160629 DOI: 10.1016/j.scr.2023.103293Associated cell lines:
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Duboscq-Bidot L, Hoareau B, Ader F, Fontaine V, Villard E
Generation of CRISPR-Cas9 edited human induced pluripotent stem cell line carrying BAG3 V468M mutation in its BAG domain
Duboscq-Bidot L et al. Generation of CRISPR-Cas9 edited human induced pluripotent stem cell line carrying BAG3 V468M mutation in its BAG domain. . 2024-02-00. Pubmed ID: 38183888; DOI: 10.1016/j.scr.2023.103294 ICANi002-A-3ICANi002-A-4 2024-02-00 2024-02-00 PubMed: 38183888 DOI: 10.1016/j.scr.2023.103294Associated cell lines:
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C M, V S, A O, S C, E R, F S, E M V
Generation of iPSC line from a Joubert syndrome patient with compound heterozygous mutations in CPLANE1 gene
C M et al. Generation of iPSC line from a Joubert syndrome patient with compound heterozygous mutations in CPLANE1 gene. . 2024-02-00. Pubmed ID: 38100914; DOI: 10.1016/j.scr.2023.103267; PMC: PMC10805004 UNIPVi004-A 2024-02-00 2024-02-00 PubMed: 38100914 DOI: 10.1016/j.scr.2023.103267Associated cell lines:
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Kadakova S, Raska J, Hribkova H, Fedorova V, Sedmik J, Plesingrova K, Sheardova K, Bohaciakova D
Generation of the Human iPSC Line from Spontaneous Late-Onset Alzheimer's Disease Patient with ApoE3/3 Genotype and Sex-, Age-, and ApoE-Matched Healthy Control
Kadakova S et al. Generation of the Human iPSC Line from Spontaneous Late-Onset Alzheimer's Disease Patient with ApoE3/3 Genotype and Sex-, Age-, and ApoE-Matched Healthy Control. . 2024-02-00. Pubmed ID: 38100913; DOI: 10.1016/j.scr.2023.103273 MUNIi020-AMUNIi021-A 2024-02-00 2024-02-00 PubMed: 38100913 DOI: 10.1016/j.scr.2023.103273Associated cell lines:
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Ishikawa KI, Shiga T, Funayama M, Hattori N, Akamatsu W
Generation of a control iPS cell line (JUCGRMi006-A) with no abnormalities in Parkinson's disease-related genes
Ishikawa KI et al. Generation of a control iPS cell line (JUCGRMi006-A) with no abnormalities in Parkinson's disease-related genes. . 2024-02-00. Pubmed ID: 38100911; DOI: 10.1016/j.scr.2023.103270 JUCGRMi006-A 2024-02-00 2024-02-00 PubMed: 38100911 DOI: 10.1016/j.scr.2023.103270Associated cell lines:
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Yang X, Fan Y, Li Y, Zhang H, Wang B, Guan J, Gao J, Ma X, Liu Y
Generation and characterization of PBMCs-derived human induced pluripotent stem cell (iPSC) line SDQLCHi050-A from a healthy donor
Yang X et al. Generation and characterization of PBMCs-derived human induced pluripotent stem cell (iPSC) line SDQLCHi050-A from a healthy donor. . 2024-02-00. Pubmed ID: 38128452; DOI: 10.1016/j.scr.2023.103266 SDQLCHi044-ASDQLCHi050-A 2024-02-00 2024-02-00 PubMed: 38128452 DOI: 10.1016/j.scr.2023.103266Associated cell lines:
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Lahm H, Singh NK, Gottmann I, Doppler SA, Dzilic E, Preisler H, Schneider S, Lange R, Krane M, Dreßen M
Insertion of a FLAG-tag sequence at the end of exon 9 of the TBX5 gene in three induced pluripotent stem cell lines (DHMi004-A-4, DHMi004-A-5, DHMi004-A-6) by CRISPR/Cas9 technology
Lahm H et al. Insertion of a FLAG-tag sequence at the end of exon 9 of the TBX5 gene in three induced pluripotent stem cell lines (DHMi004-A-4, DHMi004-A-5, DHMi004-A-6) by CRISPR/Cas9 technology. . 2024-02-00. Pubmed ID: 38100916; DOI: 10.1016/j.scr.2023.103261 DHMi004-ADHMi004-A-4DHMi004-A-5DHMi004-A-6 2024-02-00 2024-02-00 PubMed: 38100916 DOI: 10.1016/j.scr.2023.103261Associated cell lines:
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Qiu B, Zheng W, Zhong Y, Liu H, Yu J, Luo Y, Liu J, Yang B
Generation of a human embryonic stem cell line (SMUDHe010-A-1B) carrying inducible DTA expression cassette in the AAVS1 locus by CRISPR/Cas9-mediated homologous recombination
Qiu B et al. Generation of a human embryonic stem cell line (SMUDHe010-A-1B) carrying inducible DTA expression cassette in the AAVS1 locus by CRISPR/Cas9-mediated homologous recombination. . 2024-02-00. Pubmed ID: 38103335; DOI: 10.1016/j.scr.2023.103283 WAe009-A-1B 2024-02-00 2024-02-00 PubMed: 38103335 DOI: 10.1016/j.scr.2023.103283Associated cell lines:
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Eberl H, Rebs S, Hoppe S, Sedaghat-Hamedani F, Kayvanpour E, Meder B, Streckfuss-Bömeke K
Generation of an RBM20-mutation-associated left-ventricular non-compaction cardiomyopathy iPSC line (UMGi255-A) into a DCM genetic background to investigate monogenetic cardiomyopathies
Eberl H et al. Generation of an RBM20-mutation-associated left-ventricular non-compaction cardiomyopathy iPSC line (UMGi255-A) into a DCM genetic background to investigate monogenetic cardiomyopathies. . 2024-02-00. Pubmed ID: 38141360; DOI: 10.1016/j.scr.2023.103290 UMGi255-A 2024-02-00 2024-02-00 PubMed: 38141360 DOI: 10.1016/j.scr.2023.103290Associated cell lines:
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Douglas M, O'Loughlin C, Lynch AT, Prialgauskaite R, Adamson AD, Dibb KM, Kimber SJ, Birket MJ
The generation and validation of two NKX2-5 fluorescent reporter human embryonic stem cell lines: UMANe002-A-1 and UMANe002-A-2
Douglas M et al. The generation and validation of two NKX2-5 fluorescent reporter human embryonic stem cell lines: UMANe002-A-1 and UMANe002-A-2. . 2024-02-00. Pubmed ID: 38100908; DOI: 10.1016/j.scr.2023.103262 UMANe002-AUMANe002-A-1UMANe002-A-2 2024-02-00 2024-02-00 PubMed: 38100908 DOI: 10.1016/j.scr.2023.103262Associated cell lines:
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Chen Genghua, Chen Jiahui, Qi Lin, Yin Yunqian, Lin Zetong, Wen Huaqiang, Zhang Shuai, Xiao Chuanyun, Bello Semiu Folaniyi, Zhang Xiquan, Nie Qinghua, Luo Wen
Bulk and single‐cell alternative splicing analyses reveal roles of
Chen Genghua et al. Bulk and single‐cell alternative splicing analyses reveal roles ofTRA2B in myogenic differentiationTRA2B in myogenic differentiation. . 2024-02-00. DOI: 10.1111/cpr.13545 SDQLCHi004-A 2024-02-00 2024-02-00 DOI: 10.1111/cpr.13545Associated cell lines:
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Aleo Serena Jasmine, Del Dotto Valentina, Romagnoli Martina, Fiorini Claudio, Capirossi Giada, Peron Camille, Maresca Alessandra, Caporali Leonardo, Capristo Mariantonietta, Tropeano Concetta Valentina, Zanna Claudia, Ross-Cisneros Fred N., Sadun Alfredo A., Pignataro Maria Gemma, Giordano Carla, Fasano Chiara, Cavaliere Andrea, Porcelli Anna Maria, Tioli Gaia, Musiani Francesco, Catania Alessia, Lamperti Costanza, Marzoli Stefania Bianchi, De Negri Annamaria, Cascavilla Maria Lucia, Battista Marco, Barboni Piero, Carbonelli Michele, Amore Giulia, La Morgia Chiara, Smirnov Dmitrii, Vasilescu Catalina, Farzeen Aiman, Blickhaeuser Beryll, Prokisch Holger, Priglinger Claudia, Livonius Bettina, Catarino Claudia B., Klopstock Thomas, Tiranti Valeria, Carelli Valerio, Ghelli Anna Maria
Genetic variants affecting NQO1 protein levels impact the efficacy of idebenone treatment in Leber hereditary optic neuropathy
Aleo Serena Jasmine et al. Genetic variants affecting NQO1 protein levels impact the efficacy of idebenone treatment in Leber hereditary optic neuropathy. . 2024-02-00. DOI: 10.1016/j.xcrm.2023.101383 FINCBi001-A 2024-02-00 2024-02-00 DOI: 10.1016/j.xcrm.2023.101383Associated cell lines:
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Ahmad I, Kapoor H, Kumar Srivastava A, Faruq M
Generation and characterization of two human iPSC lines, IGIBi014-A and IGIBi015-A, from Friedreich's ataxia (FRDA) patients with pathogenic (GAA/TTC)n repeat expansion in first intron of the Frataxin (FXN) gene
Ahmad I et al. Generation and characterization of two human iPSC lines, IGIBi014-A and IGIBi015-A, from Friedreich's ataxia (FRDA) patients with pathogenic (GAA/TTC)n repeat expansion in first intron of the Frataxin (FXN) gene. . 2024-02-00. Pubmed ID: 38141359; DOI: 10.1016/j.scr.2023.103289 IGIBi006-AIGIBi008-AIGIBi014-AIGIBi015-A 2024-02-00 2024-02-00 PubMed: 38141359 DOI: 10.1016/j.scr.2023.103289Associated cell lines:
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Ishikawa KI, Shiga T, Funayama M, Hattori N, Akamatsu W
Generation of a control iPS cell line (JUCGRMi005-A) with no abnormalities in Parkinson's disease-related genes
Ishikawa KI et al. Generation of a control iPS cell line (JUCGRMi005-A) with no abnormalities in Parkinson's disease-related genes. . 2024-02-00. Pubmed ID: 38100917; DOI: 10.1016/j.scr.2023.103271 JUCGRMi005-A 2024-02-00 2024-02-00 PubMed: 38100917 DOI: 10.1016/j.scr.2023.103271Associated cell lines:
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Li Y, Zhang H, Guan J, Wang B, Zhang H, Liu Y, Gai Z
Generation of an iPSC line (SDQLCHi030-A) derived from PBMCs of a patient with Lesch-Nyhan syndrome caused by HPRT1 mutation
Li Y et al. Generation of an iPSC line (SDQLCHi030-A) derived from PBMCs of a patient with Lesch-Nyhan syndrome caused by HPRT1 mutation. . 2024-02-00. Pubmed ID: 38154384; DOI: 10.1016/j.scr.2023.103287 SDQLCHi030-A 2024-02-00 2024-02-00 PubMed: 38154384 DOI: 10.1016/j.scr.2023.103287Associated cell lines:
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Wang Yan, Xu Lizhen, Zhang Ying, Fu Haidong, Gao Langping, Guan Yuelin, Gu Weizhong, Sun Jingmiao, Chen Xiangjun, Yang Fan, Lai EnYin, Wang Jingjing, Jin Yanyan, Kou Ziqi, Qiu Xingyu, Mao Jianhua, Hu Lidan
Dent disease 1-linked novel CLCN5 mutations result in aberrant location and reduced ion currents
Wang Yan et al. Dent disease 1-linked novel CLCN5 mutations result in aberrant location and reduced ion currents. . 2024-02-00. DOI: 10.1016/j.ijbiomac.2023.128564 NCKDi003-A 2024-02-00 2024-02-00 DOI: 10.1016/j.ijbiomac.2023.128564Associated cell lines:
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Sharma Rakesh
Innovative Genoceuticals in Human Gene Therapy Solutions: Challenges and Safe Clinical Trials of Orphan Gene Therapy Products
Sharma Rakesh. Innovative Genoceuticals in Human Gene Therapy Solutions: Challenges and Safe Clinical Trials of Orphan Gene Therapy Products. . 2024-02-00. DOI: 10.2174/1566523223666230911120922 USTCi001-AUSTCi001-A-1 2024-02-00 2024-02-00 DOI: 10.2174/1566523223666230911120922Associated cell lines:
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Guo Y, Li J, Xie W, Huang H, Li JJ, Lin W, Lu YQ
Generation of an integration-free induced pluripotent stem cell line, FJMUUHi002-A, from a Rett syndrome patient with a heterozygous mutation p. R133C in MeCP2
Guo Y et al. Generation of an integration-free induced pluripotent stem cell line, FJMUUHi002-A, from a Rett syndrome patient with a heterozygous mutation p. R133C in MeCP2. . 2024-02-00. Pubmed ID: 38100910; DOI: 10.1016/j.scr.2023.103268 FJMUUHi002-A 2024-02-00 2024-02-00 PubMed: 38100910 DOI: 10.1016/j.scr.2023.103268Associated cell lines:
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Wang Jingwen, Zhang Lei, Wu Guanglan, Wu Jinni, Zhou Xinyao, Chen Xiaolin, Niu Yongxia, Jiao Yiren, Liu Qianyi, Liang Puping, Shi Guang, Wu Xueqing, Huang Junjiu
Correction of a CADASIL point mutation using adenine base editors in hiPSCs and blood vessel organoids
Wang Jingwen et al. Correction of a CADASIL point mutation using adenine base editors in hiPSCs and blood vessel organoids. . 2024-02-00. DOI: 10.1016/j.jgg.2023.04.013 IDISi001-A 2024-02-00 2024-02-00 DOI: 10.1016/j.jgg.2023.04.013Associated cell lines:
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Zaker Erfan, Nouri Negar, Movahedinia Mojtaba, Dadbinpour Ali, Vahidi Mehrjardi Mohammad Yahya
Type 1 early infantile epileptic encephalopathy: A case report and literature review
Zaker Erfan et al. Type 1 early infantile epileptic encephalopathy: A case report and literature review. . 2024-02-00. DOI: 10.1002/mgg3.2412 OGHFUi001-A 2024-02-00 2024-02-00 DOI: 10.1002/mgg3.2412Associated cell lines:
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Aljuhani M, Choudhury TZ, Yu Y, Ye S, Zhao M, Garg V
Generation and characterization of a human induced pluripotent stem cell line heterozygous for a NOTCH1 mutation (NCHi014-A)
Aljuhani M et al. Generation and characterization of a human induced pluripotent stem cell line heterozygous for a NOTCH1 mutation (NCHi014-A). . 2024-02-00. Pubmed ID: 38118204; DOI: 10.1016/j.scr.2023.103281; PMC: PMC10845017 NCHi014-A 2024-02-00 2024-02-00 PubMed: 38118204 DOI: 10.1016/j.scr.2023.103281Associated cell lines:
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Erol Özgür Doğuş, Şenocak Şimal, Aerts-Kaya Fatima
The Role of Rab GTPases in the development of genetic and malignant diseases
Erol Özgür Doğuş et al. The Role of Rab GTPases in the development of genetic and malignant diseases. . 2024-02-00. DOI: 10.1007/s11010-023-04727-x ZZUi005-A 2024-02-00 2024-02-00 DOI: 10.1007/s11010-023-04727-xAssociated cell lines:
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Kondrateva E. V., Grigorieva O. V., Kurshakova E. V., Panchuk I. O., Pozhitnova V. O., Voronina E. S., Tabakov V. Yu., Nikishina I. P., Arsenyeva S. V., Matkava V. G., Lavrov A. V., Smirnikhina S. A., Kutsev S. I.
Creation of Induced Pluripotent Stem Cells RCMGi014-A Using Reprogramming of Urine Cells of a Patient with Fibrodysplasia Ossificans Progressiva Associated with Heterozygous Mutation in the ACVR1 Gene
Kondrateva E. V. et al. Creation of Induced Pluripotent Stem Cells RCMGi014-A Using Reprogramming of Urine Cells of a Patient with Fibrodysplasia Ossificans Progressiva Associated with Heterozygous Mutation in the ACVR1 Gene. . 2024-02-00. DOI: 10.1134/s1062360424700048 RCMGi014-A 2024-02-00 2024-02-00 DOI: 10.1134/s1062360424700048Associated cell lines:
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Gao Yuan, Peng Lu, Zhao Cuifen
MYH7 in cardiomyopathy and skeletal muscle myopathy
Gao Yuan et al. MYH7 in cardiomyopathy and skeletal muscle myopathy. . 2024-02-00. DOI: 10.1007/s11010-023-04735-x WAe009-AZZUNEUi007-AICGi019-AICGi019-BMHHi021-AMHHi021-BZZUNEUi016-AZZUNEUi020-AWAe009-A-69 2024-02-00 2024-02-00 DOI: 10.1007/s11010-023-04735-xAssociated cell lines:
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Mendonca D, Cappuccio G, Sheppard J, Delacruz M, Bengtsson J, Carvalho CMB, Bajic A, Park H, Kim JJ, Jafar-Nejad P, Coquery C, Pehlivan D, Suter B, Maletic-Savatic M
Generation of five induced pluripotent stem cell lines from patients with MECP2 Duplication Syndrome
Mendonca D et al. Generation of five induced pluripotent stem cell lines from patients with MECP2 Duplication Syndrome. . 2024-02-00. Pubmed ID: 38154383; DOI: 10.1016/j.scr.2023.103292; PMC: PMC10898976 BCMi003-ABCMi004-ABCMi005-ABCMi006-ABCMi007-A 2024-02-00 2024-02-00 PubMed: 38154383 DOI: 10.1016/j.scr.2023.103292 -
Tang M, Xiong M, Zhou W, Lei J, Huang M, Huang C, Wang F, Liu J, Li J, Xu X
Generation of a human induced pluripotent stem cell line (SMUSHi002-A) from an ALS patient carrying a heterozygous mutation c.1562G > A in the FUS gene
Tang M et al. Generation of a human induced pluripotent stem cell line (SMUSHi002-A) from an ALS patient carrying a heterozygous mutation c.1562G > A in the FUS gene. . 2024-02-00. Pubmed ID: 38141357; DOI: 10.1016/j.scr.2023.103286 SMUSHi002-A 2024-02-00 2024-02-00 PubMed: 38141357 DOI: 10.1016/j.scr.2023.103286Associated cell lines:
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Wen S, Fu S, Gao C, Lei K, Liu X
Generation of two induced pluripotent stem cell lines from two sporadic amyotrophic lateral sclerosis patients
Wen S et al. Generation of two induced pluripotent stem cell lines from two sporadic amyotrophic lateral sclerosis patients. . 2024-02-00. Pubmed ID: 38181637; DOI: 10.1016/j.scr.2023.103288 WUi001-AWUi002-A 2024-02-00 2024-02-00 PubMed: 38181637 DOI: 10.1016/j.scr.2023.103288 -
Sandelin S, Hakala S, Lehtinen L, Närvä E
Generation of three isogenic human induced pluripotent stem cell lines from normal neonate skin fibroblasts
Sandelin S et al. Generation of three isogenic human induced pluripotent stem cell lines from normal neonate skin fibroblasts. . 2024-02-00. Pubmed ID: 38176368; DOI: 10.1016/j.scr.2023.103301 UTUi001-AUTUi001-BUTUi001-C 2024-02-00 2024-02-00 PubMed: 38176368 DOI: 10.1016/j.scr.2023.103301 -
Cheawsamoot Chanatjit, Ramchandani Rohin, Ameen Mohamed, Arthur Jennifer Ataam, Khongphatthanayothin Apichai, Karakikes Ioannis, Shotelersuk Vorasuk
Corrigendum to “Generation of human induced pluripotent stem cell lines derived from four patients with a pathogenic ALPK3 variant associated with adult-onset hypertrophic cardiomyopathy (HCM)” [Stem Cell Res. 73 (2023) 103233]
Cheawsamoot Chanatjit et al. Corrigendum to “Generation of human induced pluripotent stem cell lines derived from four patients with a pathogenic ALPK3 variant associated with adult-onset hypertrophic cardiomyopathy (HCM)” [Stem Cell Res. 73 (2023) 103233]. . 2024-02-00. DOI: 10.1016/j.scr.2023.103300 SCVIi097-ASCVIi098-A 2024-02-00 2024-02-00 DOI: 10.1016/j.scr.2023.103300Associated cell lines:
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Ribeiro M, Martins S, Carvalho T, Furtado M, Sampaio Cabral J, Brito D, Carmo-Fonseca M, da Rocha ST
Generation of induced pluripotent stem cell lines from two unrelated individuals with familial hypertrophic cardiomyopathy carrying the MYBPC3 missense c.1484G>A mutation
Ribeiro M et al. Generation of induced pluripotent stem cell lines from two unrelated individuals with familial hypertrophic cardiomyopathy carrying the MYBPC3 missense c.1484G>A mutation. . 2024-02-00. Pubmed ID: 38104429; DOI: 10.1016/j.scr.2023.103282 IBBISTi005-AIBBISTi005-BIBBISTi006-AIBBISTi006-B 2024-02-00 2024-02-00 PubMed: 38104429 DOI: 10.1016/j.scr.2023.103282Associated cell lines:
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Khokhar Y, Bhowmik A, Rui Zhao S, Cook Z, Nallamshetty S, Wu JC
Generation of induced pluripotent stem cell lines from South Asian ethnicity
Khokhar Y et al. Generation of induced pluripotent stem cell lines from South Asian ethnicity. . 2024-02-00. Pubmed ID: 38100915; DOI: 10.1016/j.scr.2023.103272; PMC: PMC10902214 SCVIi100-ASCVIi101-A 2024-02-00 2024-02-00 PubMed: 38100915 DOI: 10.1016/j.scr.2023.103272Associated cell lines:
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Ishikawa KI, Shiga T, Yoshino H, Nishioka K, Hattori N, Akamatsu W
Generation of three clones (JUCGRMi002-A, B, C) of induced pluripotent stem cells from a Parkinson's disease patient with SNCA duplication
Ishikawa KI et al. Generation of three clones (JUCGRMi002-A, B, C) of induced pluripotent stem cells from a Parkinson's disease patient with SNCA duplication. . 2024-02-00. Pubmed ID: 38154385; DOI: 10.1016/j.scr.2023.103296 JUCGRMi002-AJUCGRMi002-BJUCGRMi002-C 2024-02-00 2024-02-00 PubMed: 38154385 DOI: 10.1016/j.scr.2023.103296Associated cell lines:
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Schreiber MK, Zafeiriou MP
Generation of Pelizaeus-Merzbacher disease (PMD) mutant (PLP1-C33Y) in induced pluripotent stem cell (iPSC) by CRISPR/Cas9 genome editing
Schreiber MK et al. Generation of Pelizaeus-Merzbacher disease (PMD) mutant (PLP1-C33Y) in induced pluripotent stem cell (iPSC) by CRISPR/Cas9 genome editing. . 2024-02-00. Pubmed ID: 38104430; DOI: 10.1016/j.scr.2023.103276 RUCDRi002-A-69 2024-02-00 2024-02-00 PubMed: 38104430 DOI: 10.1016/j.scr.2023.103276Associated cell lines:
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Garcia L, Gonzalez CD, Gagne A, McGuire JA, French D, Takanohashi A, Almad A, Vanderver A, Sase S
Generation of three induced pluripotent stem cell lines from individuals with Aicardi-Goutières syndrome caused by a c.3019G>A (p.G1007R) autosomal dominant pathogenic variant in ADAR1
Garcia L et al. Generation of three induced pluripotent stem cell lines from individuals with Aicardi-Goutières syndrome caused by a c.3019G>A (p.G1007R) autosomal dominant pathogenic variant in ADAR1. . 2024-02-00. Pubmed ID: 38181636; DOI: 10.1016/j.scr.2023.103299; PMC: PMC10836393 CHOPi009-ACHOPi010-ACHOPi011-A 2024-02-00 2024-02-00 PubMed: 38181636 DOI: 10.1016/j.scr.2023.103299Associated cell lines:
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Ludwik KA, Jahn R, Schörding AK, Moeller LC, Stachelscheid H
Generation of THRB-GS(E125G_G126S) and THRB-KO human iPSC lines to study noncanonical thyroid hormone signalling
Ludwik KA et al. Generation of THRB-GS(E125G_G126S) and THRB-KO human iPSC lines to study noncanonical thyroid hormone signalling. . 2024-02-00. Pubmed ID: 38100912; DOI: 10.1016/j.scr.2023.103275 BIHi001-B-2BIHi001-B-3BIHi001-B-6 2024-02-00 2024-02-00 PubMed: 38100912 DOI: 10.1016/j.scr.2023.103275Associated cell lines:
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Zhang H, Daheron L, Cerna-Chavez R, Place EM, Huckfeldt RM, Pierce EA, Garita-Hernandez M
Generation of a human induced pluripotent stem cell line (OGIi001) from peripheral blood mononuclear cells of a healthy male donor
Zhang H et al. Generation of a human induced pluripotent stem cell line (OGIi001) from peripheral blood mononuclear cells of a healthy male donor. . 2024-02-00. Pubmed ID: 38134577; DOI: 10.1016/j.scr.2023.103280; PMC: PMC11226232 OGIi001-A 2024-02-00 2024-02-00 PubMed: 38134577 DOI: 10.1016/j.scr.2023.103280Associated cell lines:
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Jonsgaard Larsen L, Elisabeth Hjermind L, Birk Møller L
Generation of induced pluripotent stem cells, KCi005-A derived from a female with Parkinsońs disease and homozygous for the PINK1 variant c.1366C > T, p.Gln456
Jonsgaard Larsen L et al. Generation of induced pluripotent stem cells, KCi005-A derived from a female with Parkinsońs disease and homozygous for the PINK1 variant c.1366C > T, p.Gln456. . 2024-02-00. Pubmed ID: 38103334; DOI: 10.1016/j.scr.2023.103279 KCi005-A 2024-02-00 2024-02-00 PubMed: 38103334 DOI: 10.1016/j.scr.2023.103279Associated cell lines:
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Sun W, Li X, Dong J, Zhou Y
Generation of a TAB2 knockout hESC line (WAe009-A-Z) derived from H9 using CRISPR/Cas9
Sun W et al. Generation of a TAB2 knockout hESC line (WAe009-A-Z) derived from H9 using CRISPR/Cas9. . 2024-02-00. Pubmed ID: 38118206; DOI: 10.1016/j.scr.2023.103284 WAe009-AWAe009-A-Z 2024-02-00 2024-02-00 PubMed: 38118206 DOI: 10.1016/j.scr.2023.103284Associated cell lines:
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Wang L, Zeng Q, Wang S, Wu D, Wang J, Zhang H, Lv X
Establishment of an induced pluripotent stem cell line (SDCHi001-A) from a healthy Chinese child donor
Wang L et al. Establishment of an induced pluripotent stem cell line (SDCHi001-A) from a healthy Chinese child donor. . 2024-02-00. Pubmed ID: 38118205; DOI: 10.1016/j.scr.2023.103278 SDQLCHi052-ASDCHi001-A 2024-02-00 2024-02-00 PubMed: 38118205 DOI: 10.1016/j.scr.2023.103278Associated cell lines:
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Kuo Chin, Tsang Seng-Su
Constructing an Investment Scam Detection Model Based on Emotional Fluctuations Throughout the Investment Scam Life Cycle
Kuo Chin et al. Constructing an Investment Scam Detection Model Based on Emotional Fluctuations Throughout the Investment Scam Life Cycle. . 2024-02-00. DOI: 10.1080/01639625.2023.2244115 ZZUNEUi007-A 2024-02-00 2024-02-00 DOI: 10.1080/01639625.2023.2244115Associated cell lines:
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Dewal Revati S., Yang Felix T., Baer Lisa A., Vidal Pablo, Hernandez-Saavedra Diego, Seculov Nickolai P., Ghosh Adhideb, Noé Falko, Togliatti Olivia, Hughes Lexis, DeBari Megan K., West Michael D., Soroko Richard, Sternberg Hal, Malik Nafees N., Puchulu-Campanella Estella, Wang Huabao, Yan Pearlly, Wolfrum Christian, Abbott Rosalyn D., Stanford Kristin I.
Transplantation of committed pre-adipocytes from brown adipose tissue improves whole-body glucose homeostasis
Dewal Revati S. et al. Transplantation of committed pre-adipocytes from brown adipose tissue improves whole-body glucose homeostasis. . 2024-02-00. DOI: 10.1016/j.isci.2024.108927 HVRDe008-AHVRDe008-A-1 2024-02-00 2024-02-00 DOI: 10.1016/j.isci.2024.108927Associated cell lines:
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Gornostal E, Alsalloum A, Mityaeva O, Volchkov P
Generation of induced pluripotent stem line (MIPTi001-A) derived from patient with X-linked adrenoleukodystrophy (X-ALD)
Gornostal E et al. Generation of induced pluripotent stem line (MIPTi001-A) derived from patient with X-linked adrenoleukodystrophy (X-ALD). . 2024-02-00. Pubmed ID: 38176367; DOI: 10.1016/j.scr.2023.103298 MIPTi001-AABi004-A 2024-02-00 2024-02-00 PubMed: 38176367 DOI: 10.1016/j.scr.2023.103298Associated cell lines:
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Melesio J, Bonilauri B, Li A, Pang PD, Liao R, Witteles RM, Wu JC, Sallam K
Generation of two induced pluripotent stem cell lines from hereditary amyloidosis patients with polyneuropathy carrying heterozygous transthyretin (TTR) mutation
Melesio J et al. Generation of two induced pluripotent stem cell lines from hereditary amyloidosis patients with polyneuropathy carrying heterozygous transthyretin (TTR) mutation. . 2024-02-00. Pubmed ID: 38100909; DOI: 10.1016/j.scr.2023.103265; PMC: PMC10883469 SCVIi091-ASCVIi092-A 2024-02-00 2024-02-00 PubMed: 38100909 DOI: 10.1016/j.scr.2023.103265Associated cell lines:
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Gandini Maria A., Zamponi Gerald W.
Opening the KV3.1 gates: A therapeutic strategy for progressive myoclonus epilepsy type 7?
Gandini Maria A. et al. Opening the KV3.1 gates: A therapeutic strategy for progressive myoclonus epilepsy type 7?. . 2024-02-00. DOI: 10.1016/j.xcrm.2024.101425 GZHMCi001-AGZHMCi001-B 2024-02-00 2024-02-00 DOI: 10.1016/j.xcrm.2024.101425Associated cell lines:
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Zeng A, Ni K, Fang S, Yu L, Gao Y, Zhou L, Zhao X
Generation of a human iPSC line (CHCMUi002-A) from peripheral blood mononuclear cells from a chronic granulomatous disease patient
Zeng A et al. Generation of a human iPSC line (CHCMUi002-A) from peripheral blood mononuclear cells from a chronic granulomatous disease patient. . 2024-02-00. Pubmed ID: 38134578; DOI: 10.1016/j.scr.2023.103269 CHCMUi002-A 2024-02-00 2024-02-00 PubMed: 38134578 DOI: 10.1016/j.scr.2023.103269Associated cell lines:
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Paasche A, Wiedmann F, Kraft M, Seibertz F, Herlt V, Blochberger PL, Jávorszky N, Beck M, Weirauch L, Seeger T, Blank A, Haefeli WE, Arif R, Meyer AL, Warnecke G, Karck M, Voigt N, Frey N, Schmidt C
Acute antiarrhythmic effects of SGLT2 inhibitors-dapagliflozin lowers the excitability of atrial cardiomyocytes
Paasche A et al. Acute antiarrhythmic effects of SGLT2 inhibitors-dapagliflozin lowers the excitability of atrial cardiomyocytes. . 2024-02-00. Pubmed ID: 38170280; DOI: 10.1007/s00395-023-01022-0; PMC: PMC10837223 UMGi014-C 2024-02-00 2024-02-00 PubMed: 38170280 DOI: 10.1007/s00395-023-01022-0Associated cell lines:
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Ofrim M, Little D, Nazari M, Minnis CJ, Devine MJ, Mole SE, Gissen P, Lorvellec M
Characterization of two human induced pluripotent stem cell lines derived from Batten disease patient fibroblasts harbouring CLN5 mutations
Ofrim M et al. Characterization of two human induced pluripotent stem cell lines derived from Batten disease patient fibroblasts harbouring CLN5 mutations. . 2024-02-00. Pubmed ID: 38141358; DOI: 10.1016/j.scr.2023.103291 UCLi021-AUCLi022-A 2024-02-00 2024-02-00 PubMed: 38141358 DOI: 10.1016/j.scr.2023.103291 -
D’Amato Andrea, Mariani Marco Valerio, Prosperi Silvia, Colombo Lorenzo, De Prisco Andrea, Lavalle Carlo, Mancone Massimo, Vizza Carmine Dario, Severino Paolo
Spontaneous Coronary Artery Dissection in Clinical Practice: Pathophysiology and Therapeutic Approaches
D’Amato Andrea et al. Spontaneous Coronary Artery Dissection in Clinical Practice: Pathophysiology and Therapeutic Approaches. . 2024-01-26. DOI: 10.3390/medicina60020217 VCCRIi001-A 2024-01-26 2024-01-26 DOI: 10.3390/medicina60020217Associated cell lines:
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Linn AK, Manopwisedjaroen S, Kanjanasirirat P, Borwornpinyo S, Hongeng S, Phanthong P, Thitithanyanont A
Unveiling the Antiviral Properties of Panduratin A through SARS-CoV-2 Infection Modeling in Cardiomyocytes
Linn AK et al. Unveiling the Antiviral Properties of Panduratin A through SARS-CoV-2 Infection Modeling in Cardiomyocytes. . 2024-01-24. Pubmed ID: 38338708; DOI: 10.3390/ijms25031427; PMC: PMC10855687 MUi019-A 2024-01-24 2024-01-24 PubMed: 38338708 DOI: 10.3390/ijms25031427Associated cell lines:
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Pavon N, Diep K, Yang F, Sebastian R, Martinez-Martin B, Ranjan R, Sun Y, Pak C
Patterning ganglionic eminences in developing human brain organoids using a morphogen-gradient-inducing device
Pavon N et al. Patterning ganglionic eminences in developing human brain organoids using a morphogen-gradient-inducing device. . 2024-01-22. Pubmed ID: 38228151; DOI: 10.1016/j.crmeth.2023.100689; PMC: PMC10831957 WAe001-A 2024-01-22 2024-01-22 PubMed: 38228151 DOI: 10.1016/j.crmeth.2023.100689Associated cell lines:
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Cobelo-Gómez Silvia, Sánchez-Iglesias Sofía, Fernández-Pombo Antía, Araújo-Vilar David
Effect of β-Estradiol on Adipogenesis in a 3T3-L1 Cell Model of Prelamin A Accumulation
Cobelo-Gómez Silvia et al. Effect of β-Estradiol on Adipogenesis in a 3T3-L1 Cell Model of Prelamin A Accumulation. . 2024-01-20. DOI: 10.3390/ijms25021282 PUMCHi001-A 2024-01-20 2024-01-20 DOI: 10.3390/ijms25021282Associated cell lines:
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Hennegan J, Bryant AH, Griffiths L, Trigano M, Bartley OJM, Bartlett JJ, Minahan C, Abreu de Oliveira WA, Yutuc E, Ntikas S, Bartsocas CS, Markouri M, Antoniadou E, Laina I, Howell OW, Li M, Wang Y, Griffiths WJ, Lane EL, Lelos MJ, Theofilopoulos S
Inhibition of 7α,26-dihydroxycholesterol biosynthesis promotes midbrain dopaminergic neuron development
Hennegan J et al. Inhibition of 7α,26-dihydroxycholesterol biosynthesis promotes midbrain dopaminergic neuron development. . 2024-01-19. Pubmed ID: 38155767; DOI: 10.1016/j.isci.2023.108670; PMC: PMC10753067 RCe021-A 2024-01-19 2024-01-19 PubMed: 38155767 DOI: 10.1016/j.isci.2023.108670Associated cell lines:
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Vandenbempt V, Eski SE, Brahma MK, Li A, Negueruela J, Bruggeman Y, Demine S, Xiao P, Cardozo AK, Baeyens N, Martelotto LG, Singh SP, Mariño E, Gysemans C, Gurzov EN
HAMSAB diet ameliorates dysfunctional signaling in pancreatic islets in autoimmune diabetes
Vandenbempt V et al. HAMSAB diet ameliorates dysfunctional signaling in pancreatic islets in autoimmune diabetes. . 2024-01-19. Pubmed ID: 38213620; DOI: 10.1016/j.isci.2023.108694; PMC: PMC10783594 WAe001-A 2024-01-19 2024-01-19 PubMed: 38213620 DOI: 10.1016/j.isci.2023.108694Associated cell lines:
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Neehus AL, Carey B, Landekic M, Panikulam P, Deutsch G, Ogishi M, Arango-Franco CA, Philippot Q, Modaresi M, Mohammadzadeh I, Corcini Berndt M, Rinchai D, Le Voyer T, Rosain J, Momenilandi M, Martin-Fernandez M, Khan T, Bohlen J, Han JE, Deslys A, Bernard M, Gajardo-Carrasco T, Soudée C, Le Floc'h C, Migaud M, Seeleuthner Y, Jang MS, Nikolouli E, Seyedpour S, Begueret H, Emile JF, Le Guen P, Tavazzi G, Colombo CNJ, Marzani FC, Angelini M, Trespidi F, Ghirardello S, Alipour N, Molitor A, Carapito R, Mazloomrezaei M, Rokni-Zadeh H, Changi-Ashtiani M, Brouzes C, Vargas P, Borghesi A, Lachmann N, Bahram S, Crestani B, Fayon M, Galode F, Pahari S, Schlesinger LS, Marr N, Bogunovic D, Boisson-Dupuis S, Béziat V, Abel L, Borie R, Young LR, Deterding R, Shahrooei M, Rezaei N, Parvaneh N, Craven D, Gros P, Malo D, Sepulveda FE, Nogee LM, Aladjidi N, Trapnell BC, Casanova JL, Bustamante J
Human inherited CCR2 deficiency underlies progressive polycystic lung disease
Neehus AL et al. Human inherited CCR2 deficiency underlies progressive polycystic lung disease. . 2024-01-18. Pubmed ID: 38157855; DOI: 10.1016/j.cell.2023.11.036; PMC: PMC10842692 MHHi015-A 2024-01-18 2024-01-18 PubMed: 38157855 DOI: 10.1016/j.cell.2023.11.036Associated cell lines:
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Wang Chencheng, Abadpour Shadab, Olsen Petter Angell, Wang Daxin, Stokowiec Justyna, Chera Simona, Ghila Luiza, Ræder Helge, Krauss Stefan, Aizenshtadt Aleksandra, Scholz Hanne
Glucose Concentration in Regulating Induced Pluripotent Stem Cells Differentiation Toward Insulin-Producing Cells
Wang Chencheng et al. Glucose Concentration in Regulating Induced Pluripotent Stem Cells Differentiation Toward Insulin-Producing Cells. . 2024-01-18. DOI: 10.3389/ti.2024.11900 HMGUi001-AHMGUi001-A-8 2024-01-18 2024-01-18 DOI: 10.3389/ti.2024.11900Associated cell lines:
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Zanon A, Guida M, Lavdas AA, Corti C, Castelo Rueda MP, Negro A, Pramstaller PP, Domingues FS, Hicks AA, Pichler I
Intracellular delivery of Parkin-RING0-based fragments corrects Parkin-induced mitochondrial dysfunction through interaction with SLP-2
Zanon A et al. Intracellular delivery of Parkin-RING0-based fragments corrects Parkin-induced mitochondrial dysfunction through interaction with SLP-2. . 2024-01-16. Pubmed ID: 38229174; DOI: 10.1186/s12967-024-04850-3; PMC: PMC10790385 STBCi033-BEURACi005-A 2024-01-16 2024-01-16 PubMed: 38229174 DOI: 10.1186/s12967-024-04850-3Associated cell lines:
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Bombieri C, Corsi A, Trabetti E, Ruggiero A, Marchetto G, Vattemi G, Valenti MT, Zipeto D, Romanelli MG
Advanced Cellular Models for Rare Disease Study: Exploring Neural, Muscle and Skeletal Organoids
Bombieri C et al. Advanced Cellular Models for Rare Disease Study: Exploring Neural, Muscle and Skeletal Organoids. . 2024-01-13. Pubmed ID: 38256087; DOI: 10.3390/ijms25021014; PMC: PMC10815694 KSCBi006-AMCRIi019-AMCRIi019-A-7 2024-01-13 2024-01-13 PubMed: 38256087 DOI: 10.3390/ijms25021014Associated cell lines:
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Benzoni Patrizia, Gazzerro Elisabetta, Fiorillo Chiara, Baratto Serena, Bartolucci Chiara, Severi Stefano, Milanesi Raffaella, Lippi Melania, Langione Marianna, Murano Carmen, Meoni Clarissa, Popolizio Vera, Cospito Alessandro, Baruscotti Mirko, Bucchi Annalisa, Barbuti Andrea
Caveolin-3 and Caveolin-1 Interaction Decreases Channel Dysfunction Due to Caveolin-3 Mutations
Benzoni Patrizia et al. Caveolin-3 and Caveolin-1 Interaction Decreases Channel Dysfunction Due to Caveolin-3 Mutations. . 2024-01-12. DOI: 10.3390/ijms25020980 EURACi001-AEURACi002-AEURACi003-A 2024-01-12 2024-01-12 DOI: 10.3390/ijms25020980Associated cell lines:
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Sun Yu, Li Lin, Wang Jiajun, Liu Huiting, Wang Hu
Emerging Landscape of Osteogenesis Imperfecta Pathogenesis and Therapeutic Approaches
Sun Yu et al. Emerging Landscape of Osteogenesis Imperfecta Pathogenesis and Therapeutic Approaches. . 2024-01-12. DOI: 10.1021/acsptsci.3c00324 MCRIi001-AMCRIi001-A-1KSCBi006-A 2024-01-12 2024-01-12 DOI: 10.1021/acsptsci.3c00324Associated cell lines:
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Netsrithong Ratchapong, Garcia-Perez Laura, Themeli Maria
Engineered T cells from induced pluripotent stem cells: from research towards clinical implementation
Netsrithong Ratchapong et al. Engineered T cells from induced pluripotent stem cells: from research towards clinical implementation. . 2024-01-12. DOI: 10.3389/fimmu.2023.1325209 MUSIi001-AMUSIi001-A-2 2024-01-12 2024-01-12 DOI: 10.3389/fimmu.2023.1325209Associated cell lines:
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Xiao Xuliang, Zhao Yiding
G-proteins and G-protein receptors in diseases
Xiao Xuliang et al. G-proteins and G-protein receptors in diseases. . 2024-01-08. DOI: 10.1117/12.3021708 ITXi001-AITXi001-A-1 2024-01-08 2024-01-08 DOI: 10.1117/12.3021708Associated cell lines:
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Meng Xueming, Xu Cong, Li Jiawei, Qiu Benhua, Luo Jiajun, Hong Qin, Tong Yujie, Fang Chuyu, Feng Yanyan, Ma Rui, Shi Xiangyi, Lin Cheng, Pan Chen, Zhu Xueliang, Yan Xiumin, Cong Yao
Multi-scale structures of the mammalian radial spoke and divergence of axonemal complexes in ependymal cilia
Meng Xueming et al. Multi-scale structures of the mammalian radial spoke and divergence of axonemal complexes in ependymal cilia. . 2024-01-08. DOI: 10.1038/s41467-023-44577-1 MHHi019-AMHHi019-B 2024-01-08 2024-01-08 DOI: 10.1038/s41467-023-44577-1 -
Park Na Kyeong, Park Soon-Jung, Park Yun-Gwi, Moon Sung-Hwan, Woo JooHan, Kim Hyun Jong, Kim Sung Joon, Choi Seong Woo
Translation reinitiation in c.453delC frameshift mutation of KCNH2 producing functional hERG K+ channels with mild dominant negative effect in the heterozygote patient-derived iPSC cardiomyocytes
Park Na Kyeong et al. Translation reinitiation in c.453delC frameshift mutation of KCNH2 producing functional hERG K+ channels with mild dominant negative effect in the heterozygote patient-derived iPSC cardiomyocytes. . 2024-01-07. DOI: 10.1093/hmg/ddad165 KSCBi014-A 2024-01-07 2024-01-07 DOI: 10.1093/hmg/ddad165Associated cell lines:
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Jarc L, Bandral M, Zanfrini E, Lesche M, Kufrin V, Sendra R, Pezzolla D, Giannios I, Khattak S, Neumann K, Ludwig B, Gavalas A
Regulation of multiple signaling pathways promotes the consistent expansion of human pancreatic progenitors in defined conditions
Jarc L et al. Regulation of multiple signaling pathways promotes the consistent expansion of human pancreatic progenitors in defined conditions. . 2024-01-05. Pubmed ID: 38180318; DOI: 10.7554/elife.89962; PMC: PMC10945307 CRTDi004-A 2024-01-05 2024-01-05 PubMed: 38180318 DOI: 10.7554/elife.89962Associated cell lines:
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Zakharova IS, Shevchenko AI, Arssan MA, Sleptcov AA, Nazarenko MS, Zarubin AA, Zheltysheva NV, Shevchenko VA, Tmoyan NA, Saaya SB, Ezhov MV, Kukharchuk VV, Parfyonova YV, Zakian SM
iPSC-Derived Endothelial Cells Reveal LDLR Dysfunction and Dysregulated Gene Expression Profiles in Familial Hypercholesterolemia
Zakharova IS et al. iPSC-Derived Endothelial Cells Reveal LDLR Dysfunction and Dysregulated Gene Expression Profiles in Familial Hypercholesterolemia. . 2024-01-05. Pubmed ID: 38255763; DOI: 10.3390/ijms25020689; PMC: PMC10815294 ICGi021-AICGi022-AICGi036-AICGi037-AICGi038-A 2024-01-05 2024-01-05 PubMed: 38255763 DOI: 10.3390/ijms25020689 -
Summers Kim M
Genetic models of fibrillinopathies
Summers Kim M. Genetic models of fibrillinopathies. . 2024-01-03. DOI: 10.1093/genetics/iyad189 ICSSUi001-A 2024-01-03 2024-01-03 DOI: 10.1093/genetics/iyad189Associated cell lines:
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Ladero Miguel, Reche-Sainz Jose Alberto, Gallardo M. Esther
Hereditary Optic Neuropathies: A Systematic Review on the Interplay between Biomaterials and Induced Pluripotent Stem Cells
Ladero Miguel et al. Hereditary Optic Neuropathies: A Systematic Review on the Interplay between Biomaterials and Induced Pluripotent Stem Cells. . 2024-01-03. DOI: 10.3390/bioengineering11010052 IISHDOi001-AIISHDOi002-AIISHDOi003-AIISHDOi004-A 2024-01-03 2024-01-03 DOI: 10.3390/bioengineering11010052Associated cell lines:
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Zhu Y, Burg T, Neyrinck K, Vervliet T, Nami F, Vervoort E, Ahuja K, Sassano ML, Chai YC, Tharkeshwar AK, De Smedt J, Hu H, Bultynck G, Agostinis P, Swinnen JV, Van Den Bosch L, da Costa RFM, Verfaillie C
Disruption of MAM integrity in mutant FUS oligodendroglial progenitors from hiPSCs
Zhu Y et al. Disruption of MAM integrity in mutant FUS oligodendroglial progenitors from hiPSCs. . 2024-01-03. Pubmed ID: 38170217; DOI: 10.1007/s00401-023-02666-x; PMC: PMC10764485 SIGi001-A 2024-01-03 2024-01-03 PubMed: 38170217 DOI: 10.1007/s00401-023-02666-xAssociated cell lines:
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Volkmar Fred R., Woodbury-Smith Marc
Whither Asperger’s Post DSM-5? An Opinion Piece
Volkmar Fred R. et al. Whither Asperger’s Post DSM-5? An Opinion Piece. . 2024-01-03. DOI: 10.1007/s40489-023-00425-y SDUKIi003-A 2024-01-03 2024-01-03 DOI: 10.1007/s40489-023-00425-yAssociated cell lines:
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Luo Yi, Wu Kaiwen, Zhang Xiaolong, Wang Hongyang, Wang Qiuju
Genetic correction of induced pluripotent stem cells from a DFNA36 patient results in morphologic and functional recovery of derived hair cell-like cells
Luo Yi et al. Genetic correction of induced pluripotent stem cells from a DFNA36 patient results in morphologic and functional recovery of derived hair cell-like cells. . 2024-01-02. DOI: 10.1186/s13287-023-03617-9 CPGHi001-ACPGHi001-A-1 2024-01-02 2024-01-02 DOI: 10.1186/s13287-023-03617-9Associated cell lines:
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Amer-Sarsour Fatima, Falik Daniel, Berdichevsky Yevgeny, Kordonsky Alina, Eid Sharbel, Rabinski Tatiana, Ishtayeh Hasan, Cohen-Adiv Stav, Braverman Itzhak, Blumen Sergiu C, Laviv Tal, Prag Gali, Vatine Gad D, Ashkenazi Avraham
Disease-associated polyalanine expansion mutations impair UBA6-dependent ubiquitination
Amer-Sarsour Fatima et al. Disease-associated polyalanine expansion mutations impair UBA6-dependent ubiquitination. . 2024-01-02. DOI: 10.1038/s44318-023-00018-9 BGUi004-ABGUi005-A 2024-01-02 2024-01-02 DOI: 10.1038/s44318-023-00018-9 -
Saldana-Guerrero I, Montano-Gutierrez L, Boswell K, Hafemeister C, Poon E, Shaw L, Stavish D, Lea R, Wernig-Zorc S, Bozsaky E, Fetahu I, Zoescher P, Pötschger U, Bernkopf M, Wenninger-Weinzierl A, Sturtzel C, Souilhol C, Tarelli S, Shoeb M, Bozatzi P, Rados M, Guarini M, Buri M, Weninger W, Putz E, Huang M, Ladenstein R, Andrews P, Barbaric I, Cresswell G, Bryant H, Distel M, Chesler L, Taschner-Mandl S, Farlik M, Tsakiridis A, Halbritter F.
A human neural crest model reveals the developmental impact of neuroblastoma-associated chromosomal aberrations
Saldana-Guerrero I et al. A human neural crest model reveals the developmental impact of neuroblastoma-associated chromosomal aberrations. . 2024-01-01. WAe007-AWAe009-A 2024-01-01 2024-01-01 -
Yan S.
Application of the crispr/cas system in gene editing and nucleic acid detection of parasitic diseases: A review
Yan S.. Application of the crispr/cas system in gene editing and nucleic acid detection of parasitic diseases: A review. . 2024-01-01. DOI: 10.16250/j.32.1374.2024057 DHMi005-ADHMi005-A-1 2024-01-01 2024-01-01 DOI: 10.16250/j.32.1374.2024057Associated cell lines:
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Ahmed D.F.
Role of Hematopoietic Growth Factors as Immune Modulators (GM-CSF & IL-3) in Newly Diagnosed Colorectal Cancer Patients and their Correlation with P53 Expression and Global DNA Methylation
Ahmed D.F.. Role of Hematopoietic Growth Factors as Immune Modulators (GM-CSF & IL-3) in Newly Diagnosed Colorectal Cancer Patients and their Correlation with P53 Expression and Global DNA Methylation. . 2024-01-01. DOI: 10.24996/ijs.2024.65.6.8 PUMCi001-A 2024-01-01 2024-01-01 DOI: 10.24996/ijs.2024.65.6.8Associated cell lines:
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Winn D, Uhlin E, Kele M, Eidhof I, Falk A.
Pre-clinical evaluation of clinically relevant iPS cell derived neuroepithelial stem cells as an off-the-shelf cell therapy for spinal cord injury
Winn D et al. Pre-clinical evaluation of clinically relevant iPS cell derived neuroepithelial stem cells as an off-the-shelf cell therapy for spinal cord injury. . 2024-01-01. KICRi001-A 2024-01-01 2024-01-01Associated cell lines:
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Thamamongood Thiprampai, Jengarn Juggragarn, Muangsanit Papon, Petpiroon Nalinrat, Srisutthisamphan Kanjana, Attasombat Khemphitcha, Wongwanakul Ratjika, Aueviriyavit Sasitorn, Laohathai Sira, Jongkaewwattana Anan, Teeravechyan Samaporn
Pseudotyped zoonotic thogotoviruses exhibit broad entry range in mammalian cells
Thamamongood Thiprampai et al. Pseudotyped zoonotic thogotoviruses exhibit broad entry range in mammalian cells. . 2024-01-00. DOI: 10.1016/j.virol.2023.109914 MUSIi011-AMUSIi011-B 2024-01-00 2024-01-00 DOI: 10.1016/j.virol.2023.109914Associated cell lines:
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Gomez Ramos B, Ohnmacht J, de Lange N, Valceschini E, Ginolhac A, Catillon M, Ferrante D, Rakovic A, Halder R, Massart F, Arena G, Antony P, Bolognin S, Klein C, Krause R, Schulz MH, Sauter T, Krüger R, Sinkkonen L
Multiomics analysis identifies novel facilitators of human dopaminergic neuron differentiation
Gomez Ramos B et al. Multiomics analysis identifies novel facilitators of human dopaminergic neuron differentiation. . 2024-01-00. Pubmed ID: 38177910; DOI: 10.1038/s44319-023-00024-2; PMC: PMC10897179 STBCi033-BLUEi013-A 2024-01-00 2024-01-00 PubMed: 38177910 DOI: 10.1038/s44319-023-00024-2Associated cell lines:
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Jin Zhe-Long, Xu KangHe, Kim Jonghun, Guo Hao, Yao Xuerui, Xu Yong-Nan, Li Ying-Hua, Ryu DongHee, Kim Kee-Pyo, Hong Kwonho, Kim Yong-June, Wang Lin, Cao Qilong, Kim Kyun-Hwan, Kim Nam-Hyung, Han Dong Wook
3D hepatic organoid production from human pluripotent stem cells
Jin Zhe-Long et al. 3D hepatic organoid production from human pluripotent stem cells. . 2024-01-00. DOI: 10.1016/j.diff.2023.100742 OFi001-AOFi002-A 2024-01-00 2024-01-00 DOI: 10.1016/j.diff.2023.100742 -
Khatun M, Lundin K, Naillat F, Loog L, Saarela U, Tuuri T, Salumets A, Piltonen TT, Tapanainen JS
Induced Pluripotent Stem Cells as a Possible Approach for Exploring the Pathophysiology of Polycystic Ovary Syndrome (PCOS)
Khatun M et al. Induced Pluripotent Stem Cells as a Possible Approach for Exploring the Pathophysiology of Polycystic Ovary Syndrome (PCOS). . 2024-01-00. Pubmed ID: 37768523; DOI: 10.1007/s12015-023-10627-w; PMC: PMC10799779 AMUFAHi002-A 2024-01-00 2024-01-00 PubMed: 37768523 DOI: 10.1007/s12015-023-10627-wAssociated cell lines:
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Hazrati Raheleh, Davaran Soodabeh, Keyhanvar Peyman, Soltani Somaieh, Alizadeh Effat
A Systematic Review of Stem Cell Differentiation into Keratinocytes for Regenerative Applications
Hazrati Raheleh et al. A Systematic Review of Stem Cell Differentiation into Keratinocytes for Regenerative Applications. . 2024-01-00. DOI: 10.1007/s12015-023-10636-9 TCIERi001-A 2024-01-00 2024-01-00 DOI: 10.1007/s12015-023-10636-9Associated cell lines:
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Levchenko Olga, Panchuk Irina, Kochergin-Nikitsky Konstantin, Petrova Irina, Nagieva Sabina, Pilkin Maxim, Yakovlev Ivan, Smirnikhina Svetlana, Deev Roman, Lavrov Alexander
Unexpected extra exon skipping in the DYSF gene during restoring the reading frame by CRISPR/Cas9
Levchenko Olga et al. Unexpected extra exon skipping in the DYSF gene during restoring the reading frame by CRISPR/Cas9. . 2024-01-00. DOI: 10.1016/j.biosystems.2023.105072 DMBi001-ADMBi001-A-1 2024-01-00 2024-01-00 DOI: 10.1016/j.biosystems.2023.105072Associated cell lines:
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Guo Guangli, Wang Lu, Li Xiaowei, Fu Wanrong, Cao Jinhua, Zhang Jianchao, Liu Yangyang, Liu Mengduan, Wang Mengyu, Zhao Guojun, Zhao Xi, Zhou Yangfan, Niu Shaohui, Liu Gangqiong, Zhang Yanzhou, Dong Jianzeng, Tao Hailong, Zhao Xiaoyan
Enhanced myofilament calcium sensitivity aggravates abnormal calcium handling and diastolic dysfunction in patient-specific induced pluripotent stem cell-derived cardiomyocytes with MYH7 mutation
Guo Guangli et al. Enhanced myofilament calcium sensitivity aggravates abnormal calcium handling and diastolic dysfunction in patient-specific induced pluripotent stem cell-derived cardiomyocytes with MYH7 mutation. . 2024-01-00. DOI: 10.1016/j.ceca.2023.102822 ZZUNEUi016-A 2024-01-00 2024-01-00 DOI: 10.1016/j.ceca.2023.102822Associated cell lines:
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Şen Başak, Balcı‐Peynircioğlu Banu
Cellular models in autoinflammatory disease research
Şen Başak et al. Cellular models in autoinflammatory disease research. . 2024-01-00. DOI: 10.1002/cti2.1481 NIHTVBi014-ANIHTVBi016-ANIHTVBi017-ANIHTVBi018-A 2024-01-00 2024-01-00 DOI: 10.1002/cti2.1481Associated cell lines:
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Kesidou Despoina, Bennett Matthew, Monteiro João P., McCracken Ian R., Klimi Eftychia, Rodor Julie, Condie Alison, Cowan Scott, Caporali Andrea, Wit Jan B.M., Mountford Joanne C., Brittan Mairi, Beqqali Abdelaziz, Baker Andrew H.
Extracellular vesicles from differentiated stem cells contain novel proangiogenic miRNAs and induce angiogenic responses at low doses
Kesidou Despoina et al. Extracellular vesicles from differentiated stem cells contain novel proangiogenic miRNAs and induce angiogenic responses at low doses. . 2024-01-00. DOI: 10.1016/j.ymthe.2023.11.023 RCe015-A 2024-01-00 2024-01-00 DOI: 10.1016/j.ymthe.2023.11.023Associated cell lines:
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Tatwavedi Dharamveer, Pellagatti Andrea, Boultwood Jacqueline
Recent advances in the application of induced pluripotent stem cell technology to the study of myeloid malignancies
Tatwavedi Dharamveer et al. Recent advances in the application of induced pluripotent stem cell technology to the study of myeloid malignancies. . 2024-01-00. DOI: 10.1016/j.jbior.2023.100993 CHOPi001-A 2024-01-00 2024-01-00 DOI: 10.1016/j.jbior.2023.100993Associated cell lines:
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Cota P, Caliskan ÖS, Bastidas-Ponce A, Jing C, Jaki J, Saber L, Czarnecki O, Taskin D, Blöchinger AK, Kurth T, Sterr M, Burtscher I, Krahmer N, Lickert H, Bakhti M
Insulin regulates human pancreatic endocrine cell differentiation in vitro
Cota P et al. Insulin regulates human pancreatic endocrine cell differentiation in vitro. . 2024-01-00. Pubmed ID: 38103636; DOI: 10.1016/j.molmet.2023.101853; PMC: PMC10765254 HMGUi001-AHMGUi001-A-43 2024-01-00 2024-01-00 PubMed: 38103636 DOI: 10.1016/j.molmet.2023.101853Associated cell lines:
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Janz A, Walz K, Cirnu A, Surjanto J, Urlaub D, Leskien M, Kohlhaas M, Nickel A, Brand T, Nose N, Wörsdörfer P, Wagner N, Higuchi T, Maack C, Dudek J, Lorenz K, Klopocki E, Ergün S, Duff HJ, Gerull B
Mutations in DNAJC19 cause altered mitochondrial structure and increased mitochondrial respiration in human iPSC-derived cardiomyocytes
Janz A et al. Mutations in DNAJC19 cause altered mitochondrial structure and increased mitochondrial respiration in human iPSC-derived cardiomyocytes. . 2024-01-00. Pubmed ID: 38142971; DOI: 10.1016/j.molmet.2023.101859; PMC: PMC10792641 LIBUCi001-ALIBUCi002-AJMUi001-AJMUi001-A-1 2024-01-00 2024-01-00 PubMed: 38142971 DOI: 10.1016/j.molmet.2023.101859Associated cell lines:
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Wen Jie, Song Jian, Chen Jiale, Feng Zhili, Jing Qiancheng, Gong Wei, Kang Xiaoming, Mei Lingyun, He Chufeng, Ma Lu, Feng Yong
Modeling of pigmentation disorders associated with MITF mutation in Waardenburg syndrome revealed an impaired melanogenesis pathway in
Wen Jie et al. Modeling of pigmentation disorders associated with MITF mutation in Waardenburg syndrome revealed an impaired melanogenesis pathway iniPS ‐derived melanocytesiPS ‐derived melanocytes. . 2024-01-00. DOI: 10.1111/pcmr.13118 CSUXHi003-ACSUXHi004-A 2024-01-00 2024-01-00 DOI: 10.1111/pcmr.13118Associated cell lines:
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Giacalone Joseph C., Parkinson David H., Balikov Daniel A., Rao Rajesh C.
AMD and Stem Cell-Based Therapies
Giacalone Joseph C. et al. AMD and Stem Cell-Based Therapies. . 2024-01-00. DOI: 10.1097/iio.0000000000000510 JUFMDOi007-A 2024-01-00 2024-01-00 DOI: 10.1097/iio.0000000000000510Associated cell lines:
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Rassomakhina Natalia V., Ryazanova Alexandra Yu., Likhov Astemir R., Bruskin Sergey A., Maloshenok Liliya G., Zherdeva Victoria V.
Tumor Organoids: The Era of Personalized Medicine
Rassomakhina Natalia V. et al. Tumor Organoids: The Era of Personalized Medicine. . 2024-01-00. DOI: 10.1134/s0006297924140086 RCPCMi007-ARCPCMi007-A-1 2024-01-00 2024-01-00 DOI: 10.1134/s0006297924140086Associated cell lines:
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Dubau Marla, Tripetchr Tarada, Mahmoud Lava, Kral Vivian, Kleuser Burkhard
Advancing skin model development: A focus on a self-assembled, induced pluripotent stem cell-derived, xeno-free approach
Dubau Marla et al. Advancing skin model development: A focus on a self-assembled, induced pluripotent stem cell-derived, xeno-free approach. . 2024-01-00. DOI: 10.1177/20417314241291848 MUSIi006-A 2024-01-00 2024-01-00 DOI: 10.1177/20417314241291848Associated cell lines:
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Gupta Mohit, Jaabir M.S. Mohammed, Mohammad A. Akbarsha, Gomathinayagam Rohini
Cellular Reprogramming, Transdifferentiation and Alleviation of the Aging Pathology
Gupta Mohit et al. Cellular Reprogramming, Transdifferentiation and Alleviation of the Aging Pathology. . 2023-12-28. DOI: 10.25303/1902rjbt1270139 IBMSi012-A 2023-12-28 2023-12-28 DOI: 10.25303/1902rjbt1270139Associated cell lines:
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Yarkova ES, Grigor'eva EV, Medvedev SP, Pavlova SV, Zakian SM, Malakhova AA
IPSC-Derived Astrocytes Contribute to In Vitro Modeling of Parkinson's Disease Caused by the GBA1 N370S Mutation
Yarkova ES et al. IPSC-Derived Astrocytes Contribute to In Vitro Modeling of Parkinson's Disease Caused by the GBA1 N370S Mutation. . 2023-12-26. Pubmed ID: 38203497; DOI: 10.3390/ijms25010327; PMC: PMC10779194 HVRDe009-AICGi034-AICGi034-BICGi034-C 2023-12-26 2023-12-26 PubMed: 38203497 DOI: 10.3390/ijms25010327Associated cell lines:
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Yarkova E, Grigor’eva E, Medvedev S, Pavlova S, Zakian S, Malakhova A.
IPSC-Derived Astrocytes Contribute to In Vitro Modeling of Parkinson’s Disease Caused by the GBA1 N370S Mutation
Yarkova E et al. IPSC-Derived Astrocytes Contribute to In Vitro Modeling of Parkinson’s Disease Caused by the GBA1 N370S Mutation. . 2023-12-26. HVRDe009-AICGi034-AICGi034-BICGi034-C 2023-12-26 2023-12-26Associated cell lines:
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Luo Yumei, Chen Yapei, Ge Lingxia, Zhou Guanqing, Chen Yaoyong, Zhu Detu
Competing endogenous RNA network analysis of Turner syndrome patient-specific iPSC-derived cardiomyocytes reveals dysregulation of autosomal heart development genes by altered dosages of X-inactivation escaping non-coding RNAs
Luo Yumei et al. Competing endogenous RNA network analysis of Turner syndrome patient-specific iPSC-derived cardiomyocytes reveals dysregulation of autosomal heart development genes by altered dosages of X-inactivation escaping non-coding RNAs. . 2023-12-20. DOI: 10.1186/s13287-023-03601-3 NTUHi001-AGZHMCi008-A 2023-12-20 2023-12-20 DOI: 10.1186/s13287-023-03601-3Associated cell lines:
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Inagaki Masahito
Cell Reprogramming and Differentiation Utilizing Messenger RNA for Regenerative Medicine
Inagaki Masahito. Cell Reprogramming and Differentiation Utilizing Messenger RNA for Regenerative Medicine. . 2023-12-20. DOI: 10.3390/jdb12010001 KEIOi005-A 2023-12-20 2023-12-20 DOI: 10.3390/jdb12010001Associated cell lines:
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Urzi A, Lahmann I, Nguyen LVN, Rost BR, García-Pérez A, Lelievre N, Merritt-Garza ME, Phan HC, Bassell GJ, Rossoll W, Diecke S, Kunz S, Schmitz D, Gouti M
Efficient generation of a self-organizing neuromuscular junction model from human pluripotent stem cells
Urzi A et al. Efficient generation of a self-organizing neuromuscular junction model from human pluripotent stem cells. . 2023-12-19. Pubmed ID: 38114482; DOI: 10.1038/s41467-023-43781-3; PMC: PMC10730704 HMGUi001-AHMGUi001-A-50 2023-12-19 2023-12-19 PubMed: 38114482 DOI: 10.1038/s41467-023-43781-3Associated cell lines:
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Ozgür B, Puris E, Brachner A, Appelt-Menzel A, Oerter S, Balzer V, Holst MR, Christiansen RF, Hyldig K, Buckley ST, Kristensen M, Auriola S, Jensen A, Fricker G, Nielsen MS, Neuhaus W, Brodin B
Characterization of an iPSC-based barrier model for blood-brain barrier investigations using the SBAD0201 stem cell line
Ozgür B et al. Characterization of an iPSC-based barrier model for blood-brain barrier investigations using the SBAD0201 stem cell line. . 2023-12-19. Pubmed ID: 38115090; DOI: 10.1186/s12987-023-00501-9; PMC: PMC10731806 BIONi010-CSTBCi321-A 2023-12-19 2023-12-19 PubMed: 38115090 DOI: 10.1186/s12987-023-00501-9Associated cell lines:
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Seibertz F, Rubio T, Springer R, Popp F, Ritter M, Liutkute A, Bartelt L, Stelzer L, Haghighi F, Pietras J, Windel H, Pedrosa NDI, Rapedius M, Doering Y, Solano R, Hindmarsh R, Shi R, Tiburcy M, Bruegmann T, Kutschka I, Streckfuss-Bömeke K, Kensah G, Cyganek L, Zimmermann WH, Voigt N
Atrial fibrillation-associated electrical remodelling in human induced pluripotent stem cell-derived atrial cardiomyocytes: a novel pathway for antiarrhythmic therapy development
Seibertz F et al. Atrial fibrillation-associated electrical remodelling in human induced pluripotent stem cell-derived atrial cardiomyocytes: a novel pathway for antiarrhythmic therapy development. . 2023-12-19. Pubmed ID: 37677054; DOI: 10.1093/cvr/cvad143; PMC: PMC10730244 RUCDRi002-A 2023-12-19 2023-12-19 PubMed: 37677054 DOI: 10.1093/cvr/cvad143Associated cell lines:
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Cardo LF, Monzón-Sandoval J, Li Z, Webber C, Li M
Single-Cell Transcriptomics and In Vitro Lineage Tracing Reveals Differential Susceptibility of Human iPSC-Derived Midbrain Dopaminergic Neurons in a Cellular Model of Parkinson's Disease
Cardo LF et al. Single-Cell Transcriptomics and In Vitro Lineage Tracing Reveals Differential Susceptibility of Human iPSC-Derived Midbrain Dopaminergic Neurons in a Cellular Model of Parkinson's Disease. . 2023-12-18. Pubmed ID: 38132179; DOI: 10.3390/cells12242860; PMC: PMC10741976 WTSIi018-B 2023-12-18 2023-12-18 PubMed: 38132179 DOI: 10.3390/cells12242860Associated cell lines:
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Alowaysi M, Lehmann R, Al-Shehri M, Baadhaim M, Alzahrani H, Aboalola D, Zia A, Malibari D, Daghestani M, Alghamdi K, Haneef A, Jawdat D, Hakami F, Gomez-Cabrero D, Tegner J, Alsayegh K
HLA-based banking of induced pluripotent stem cells in Saudi Arabia
Alowaysi M et al. HLA-based banking of induced pluripotent stem cells in Saudi Arabia. . 2023-12-18. Pubmed ID: 38111036; DOI: 10.1186/s13287-023-03612-0; PMC: PMC10729375 KAIMRCi002-AKAIMRCi002-B 2023-12-18 2023-12-18 PubMed: 38111036 DOI: 10.1186/s13287-023-03612-0Associated cell lines:
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Shafi Ovais, Siddiqui Ghazia, Jaffry Hassam A.
The benign nature and rare occurrence of cardiac myxoma as a possible consequence of the limited cardiac proliferative/ regenerative potential: a systematic review
Shafi Ovais et al. The benign nature and rare occurrence of cardiac myxoma as a possible consequence of the limited cardiac proliferative/ regenerative potential: a systematic review. . 2023-12-18. DOI: 10.1186/s12885-023-11723-3 WAe009-AWAe009-A-45DHMi005-ADHMi005-A-1 2023-12-18 2023-12-18 DOI: 10.1186/s12885-023-11723-3Associated cell lines:
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Lu C, Garipler G, Dai C, Roush T, Salome-Correa J, Martin A, Liscovitch-Brauer N, Mazzoni EO, Sanjana NE
Essential transcription factors for induced neuron differentiation
Lu C et al. Essential transcription factors for induced neuron differentiation. . 2023-12-15. Pubmed ID: 38102126; DOI: 10.1038/s41467-023-43602-7; PMC: PMC10724217 NYGCe001-A 2023-12-15 2023-12-15 PubMed: 38102126 DOI: 10.1038/s41467-023-43602-7Associated cell lines:
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Vlassis A, Jensen TL, Mohr M, Jedrzejczyk DJ, Meng X, Kovacs G, Morera-Gómez M, Barghetti A, Muyo Abad S, Baumgartner RF, Natarajan KN, Nielsen LK, Warnecke T, Gill RT
CRISPR-Cas12a-integrated transgenes in genomic safe harbors retain high expression in human hematopoietic iPSC-derived lineages and primary cells
Vlassis A et al. CRISPR-Cas12a-integrated transgenes in genomic safe harbors retain high expression in human hematopoietic iPSC-derived lineages and primary cells. . 2023-12-15. Pubmed ID: 38034357; DOI: 10.1016/j.isci.2023.108287; PMC: PMC10682145 WTSIi018-BWTSIi018-B-1 2023-12-15 2023-12-15 PubMed: 38034357 DOI: 10.1016/j.isci.2023.108287Associated cell lines:
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Ilmarinen Tanja, Vattulainen Meri, Kandhavelu Jeyalakshmi, Bremond-Gignac Dominique, Aberdam Daniel, Skottman Heli
Production and Limbal Lineage Commitment of Aniridia Patient-Derived Induced Pluripotent Stem Cells
Ilmarinen Tanja et al. Production and Limbal Lineage Commitment of Aniridia Patient-Derived Induced Pluripotent Stem Cells. . 2023-12-14. DOI: 10.1093/stmcls/sxad067 UCLi013-A 2023-12-14 2023-12-14 DOI: 10.1093/stmcls/sxad067Associated cell lines:
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Boon N, Lu X, Andriessen CA, Orlovà M, Quinn PMJ, Boon CJF, Wijnholds J
Characterization and AAV-mediated CRB gene augmentation in human-derived CRB1(KO) and CRB1(KO)CRB2(+/-) retinal organoids
Boon N et al. Characterization and AAV-mediated CRB gene augmentation in human-derived CRB1(KO) and CRB1(KO)CRB2(+/-) retinal organoids. . 2023-12-14. Pubmed ID: 37886604; DOI: 10.1016/j.omtm.2023.101128; PMC: PMC10597801 LUMCi029-B-3 2023-12-14 2023-12-14 PubMed: 37886604 DOI: 10.1016/j.omtm.2023.101128Associated cell lines:
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Lin Hsiu-Chuan, Janssens Jasper, Kroell Ann-Sophie, Hornauer Philipp, Santel Malgorzata, Okamoto Ryoko, Karava Kyriaki, Priouret Marthe, Garcia Maria Pascual, Schroeter Manuel, Camp J. Gray, Treutlein Barbara
Human neuron subtype programming through combinatorial patterning with scRNA-seq readouts
Lin Hsiu-Chuan et al. Human neuron subtype programming through combinatorial patterning with scRNA-seq readouts. . 2023-12-13. DOI: 10.1101/2023.12.12.571318 UKBi013-A 2023-12-13 2023-12-13 DOI: 10.1101/2023.12.12.571318Associated cell lines:
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Lemarié L, Dargar T, Grosjean I, Gache V, Courtial EJ, Sohier J
Human Induced Pluripotent Spheroids' Growth Is Driven by Viscoelastic Properties and Macrostructure of 3D Hydrogel Environment
Lemarié L et al. Human Induced Pluripotent Spheroids' Growth Is Driven by Viscoelastic Properties and Macrostructure of 3D Hydrogel Environment. . 2023-12-13. Pubmed ID: 38136009; DOI: 10.3390/bioengineering10121418; PMC: PMC10740696 SCTi003-APGNMi001-A 2023-12-13 2023-12-13 PubMed: 38136009 DOI: 10.3390/bioengineering10121418Associated cell lines:
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Namipashaki A, Pugsley K, Liu X, Abrehart K, Lim SM, Sun G, Herold MJ, Polo JM, Bellgrove MA, Hawi Z
Integration of xeno-free single-cell cloning in CRISPR-mediated DNA editing of human iPSCs improves homogeneity and methodological efficiency of cellular disease modeling
Namipashaki A et al. Integration of xeno-free single-cell cloning in CRISPR-mediated DNA editing of human iPSCs improves homogeneity and methodological efficiency of cellular disease modeling. . 2023-12-12. Pubmed ID: 37977144; DOI: 10.1016/j.stemcr.2023.10.013; PMC: PMC10724053 MICCNi002-A 2023-12-12 2023-12-12 PubMed: 37977144 DOI: 10.1016/j.stemcr.2023.10.013Associated cell lines:
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Li Dandan, Ou Minglin, Dai Guandong, Zhu Peng, Luo Qi, Chen Jieping, Shah Zahir, Samokhvalov Igor M., Yin Lianghong, Sun Guoping, Tang Donge, Dai Yong
Genotypic Characterization of a Chinese Family with Osteogenesis Imperfecta and Generation of Disease-Specific Induced Pluripotent Stem Cells
Li Dandan et al. Genotypic Characterization of a Chinese Family with Osteogenesis Imperfecta and Generation of Disease-Specific Induced Pluripotent Stem Cells. . 2023-12-12. DOI: 10.31083/j.fbl2812336 MCRIi001-AMDCUi001-AMDCUi001-BMCRIi001-A-1KSCBi006-AFDCHi004-A 2023-12-12 2023-12-12 DOI: 10.31083/j.fbl2812336Associated cell lines:
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Zeng Y, Estapé Senti M, Labonia MCI, Papadopoulou P, Brans MAD, Dokter I, Fens MH, van Mil A, Sluijter JPG, Schiffelers RM, Vader P, Kros A
Fusogenic Coiled-Coil Peptides Enhance Lipid Nanoparticle-Mediated mRNA Delivery upon Intramyocardial Administration
Zeng Y et al. Fusogenic Coiled-Coil Peptides Enhance Lipid Nanoparticle-Mediated mRNA Delivery upon Intramyocardial Administration. . 2023-12-12. Pubmed ID: 37982378; DOI: 10.1021/acsnano.3c05341; PMC: PMC10722601 UKKi037-C 2023-12-12 2023-12-12 PubMed: 37982378 DOI: 10.1021/acsnano.3c05341Associated cell lines:
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Nandy Krittika, Babu Dinesh, Rani Sonam, Joshi Gaurav, Ijee Smitha, George Anila, Palani Dhavapriya, Premkumar Chitra, Rajesh Praveena, Vijayanand S., David Ernest, Murugesan Mohankumar, Velayudhan Shaji R.
Efficient gene editing in induced pluripotent stem cells enabled by an inducible adenine base editor with tunable expression
Nandy Krittika et al. Efficient gene editing in induced pluripotent stem cells enabled by an inducible adenine base editor with tunable expression. . 2023-12-11. DOI: 10.1038/s41598-023-42174-2 CSCRi005-AUPITTi002-AUPITTi002-A-1DHMi005-ADHMi005-A-1 2023-12-11 2023-12-11 DOI: 10.1038/s41598-023-42174-2Associated cell lines:
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Karpov Dmitry S., Sosnovtseva Anastasiia O., Pylina Svetlana V., Bastrich Asya N., Petrova Darya A., Kovalev Maxim A., Shuvalova Anastasija I., Eremkina Anna K., Mokrysheva Natalia G.
Challenges of CRISPR/Cas-Based Cell Therapy for Type 1 Diabetes: How Not to Engineer a “Trojan Horse”
Karpov Dmitry S. et al. Challenges of CRISPR/Cas-Based Cell Therapy for Type 1 Diabetes: How Not to Engineer a “Trojan Horse”. . 2023-12-10. DOI: 10.3390/ijms242417320 MUSIi001-AMUSIi001-A-2 2023-12-10 2023-12-10 DOI: 10.3390/ijms242417320Associated cell lines:
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Rifes P, Isaksson M, Rusimbi C, Ramón Santonja A, Nelander J, Laurell T, Kirkeby A
Identifying secreted biomarkers of dopaminergic ventral midbrain progenitor cells
Rifes P et al. Identifying secreted biomarkers of dopaminergic ventral midbrain progenitor cells. . 2023-12-10. Pubmed ID: 38072935; DOI: 10.1186/s13287-023-03580-5; PMC: PMC10712201 RCe021-A 2023-12-10 2023-12-10 PubMed: 38072935 DOI: 10.1186/s13287-023-03580-5Associated cell lines:
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Doni D, Cavion F, Bortolus M, Baschiera E, Muccioli S, Tombesi G, d'Ettorre F, Ottaviani D, Marchesan E, Leanza L, Greggio E, Ziviani E, Russo A, Bellin M, Sartori G, Carbonera D, Salviati L, Costantini P
Human frataxin, the Friedreich ataxia deficient protein, interacts with mitochondrial respiratory chain
Doni D et al. Human frataxin, the Friedreich ataxia deficient protein, interacts with mitochondrial respiratory chain. . 2023-12-08. Pubmed ID: 38062036; DOI: 10.1038/s41419-023-06320-y; PMC: PMC10703789 LUMCi028-A 2023-12-08 2023-12-08 PubMed: 38062036 DOI: 10.1038/s41419-023-06320-yAssociated cell lines:
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Aryan F, Detrés D, Luo CC, Kim SX, Shah AN, Bartusel M, Flynn RA, Calo E
Nucleolus activity-dependent recruitment and biomolecular condensation by pH sensing
Aryan F et al. Nucleolus activity-dependent recruitment and biomolecular condensation by pH sensing. . 2023-12-07. Pubmed ID: 37979585; DOI: 10.1016/j.molcel.2023.10.031; PMC: PMC10803072 UKKi011-A 2023-12-07 2023-12-07 PubMed: 37979585 DOI: 10.1016/j.molcel.2023.10.031Associated cell lines:
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Gkekas Ioannis, Vagiona Aimilia-Christina, Pechlivanis Nikolaos, Kastrinaki Georgia, Pliatsika Katerina, Iben Sebastian, Xanthopoulos Konstantinos, Psomopoulos Fotis E., Andrade-Navarro Miguel A., Petrakis Spyros
Intranuclear inclusions of polyQ-expanded ATXN1 sequester RNA molecules
Gkekas Ioannis et al. Intranuclear inclusions of polyQ-expanded ATXN1 sequester RNA molecules. . 2023-12-06. DOI: 10.3389/fnmol.2023.1280546 LUMCi002-ALUMCi003-ACJUHi001-A 2023-12-06 2023-12-06 DOI: 10.3389/fnmol.2023.1280546Associated cell lines:
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Pan D, Zhang X, Jin K, Jin ZB
CRX haploinsufficiency compromises photoreceptor precursor translocation and differentiation in human retinal organoids
Pan D et al. CRX haploinsufficiency compromises photoreceptor precursor translocation and differentiation in human retinal organoids. . 2023-12-05. Pubmed ID: 38049871; DOI: 10.1186/s13287-023-03590-3; PMC: PMC10696917 WAe009-A 2023-12-05 2023-12-05 PubMed: 38049871 DOI: 10.1186/s13287-023-03590-3Associated cell lines:
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Kim Hyun-Jun, Jung Da-Woon, Williams Darren R.
Keeping your strength up: induced pluripotent stem cell-based approaches for the treatment and investigation of skeletal muscle disorders
Kim Hyun-Jun et al. Keeping your strength up: induced pluripotent stem cell-based approaches for the treatment and investigation of skeletal muscle disorders. . 2023-12-04. DOI: 10.1080/26895293.2023.2207774 ICGi002-ASDQLCHi007-ASDQLCHi017-AICGi002-BICGi002-CIGIBi006-AIGIBi008-A 2023-12-04 2023-12-04 DOI: 10.1080/26895293.2023.2207774Associated cell lines:
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Binan L, Danquah S, Valakh V, Nehme R, Cleary B, Farhi S.
Simultaneous CRISPR screening and spatial transcriptomics reveals intracellular, intercellular, and functional transcriptional circuits
Binan L et al. Simultaneous CRISPR screening and spatial transcriptomics reveals intracellular, intercellular, and functional transcriptional circuits. . 2023-12-01. UCSFi001-A 2023-12-01 2023-12-01Associated cell lines:
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Batissoco Ana Carla, Cruz Dayane Bernardino, Alegria Thiago Geronimo Pires, Kobayashi Gerson, Oiticica Jeanne, Soares Netto Luis Eduardo, Passos-Bueno Maria Rita, Haddad Luciana Amaral, Mingroni Netto Regina Célia
GJB2 c.35del variant up-regulates GJA1 gene expression and affects differentiation of human stem cells
Batissoco Ana Carla et al. GJB2 c.35del variant up-regulates GJA1 gene expression and affects differentiation of human stem cells. . 2024-00-00. DOI: 10.1590/1678-4685-gmb-2023-0170 JUFMDOi004-AMMCi001-AUMi030-A 2024-00-00 2024-00-00 DOI: 10.1590/1678-4685-gmb-2023-0170Associated cell lines:
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Schwarzová B, Stüdemann T, Sönmez M, Rössinger J, Pan B, Eschenhagen T, Stenzig J, Wiegert JS, Christ T, Weinberger F
Modulating cardiac physiology in engineered heart tissue with the bidirectional optogenetic tool BiPOLES
Schwarzová B et al. Modulating cardiac physiology in engineered heart tissue with the bidirectional optogenetic tool BiPOLES. . 2023-12-00. Pubmed ID: 37863976; DOI: 10.1007/s00424-023-02869-x; PMC: PMC10730631 UKEi001-A 2023-12-00 2023-12-00 PubMed: 37863976 DOI: 10.1007/s00424-023-02869-xAssociated cell lines:
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Munshi Ingita Dey, Acharya Mansi, Mukherjee Sridip, Mani Indra
Recent development in CRISPR-Cas systems for cardiac disease
Munshi Ingita Dey et al. Recent development in CRISPR-Cas systems for cardiac disease. . 2024-00-00. DOI: 10.1016/bs.pmbts.2024.08.004 UPITTi002-AUPITTi002-A-1 2024-00-00 2024-00-00 DOI: 10.1016/bs.pmbts.2024.08.004Associated cell lines:
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Cheawsamoot C, Ramchandani R, Ameen M, Arthur Ataam J, Khongphatthanayothin A, Shotelersuk V, Karakikes I
Generation of human induced pluripotent stem cell lines derived from four patients with a pathogenic ALPK3 variant associated with adult-onset hypertrophic cardiomyopathy (HCM)
Cheawsamoot C et al. Generation of human induced pluripotent stem cell lines derived from four patients with a pathogenic ALPK3 variant associated with adult-onset hypertrophic cardiomyopathy (HCM). . 2023-12-00. Pubmed ID: 37944352; DOI: 10.1016/j.scr.2023.103233 SCVIi096-ASCVIi097-ASCVIi098-ASCVIi099-A 2023-12-00 2023-12-00 PubMed: 37944352 DOI: 10.1016/j.scr.2023.103233Associated cell lines:
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Walz K, Janz A, Klopocki E, Gerull B
Generation of a CRISPR/Cas9-edited Plakoglobin (JUP) knock-out (JMUi001-A-4) iPSC line to model the cardiac phenotype of arrhythmogenic cardiomyopathy
Walz K et al. Generation of a CRISPR/Cas9-edited Plakoglobin (JUP) knock-out (JMUi001-A-4) iPSC line to model the cardiac phenotype of arrhythmogenic cardiomyopathy. . 2023-12-00. Pubmed ID: 37995437; DOI: 10.1016/j.scr.2023.103240 JMUi001-AJMUi001-A-2JMUi001-A-3JMUi001-A-4 2023-12-00 2023-12-00 PubMed: 37995437 DOI: 10.1016/j.scr.2023.103240Associated cell lines:
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Szebényi K, Vargová I, Petrova V, Turečková J, Gibbons GM, Řehořová M, Abdelgawad M, Sándor A, Marekova D, Kwok JCF, Jendelová P, Fawcett JW, Lakatos A
Inhibition of PHLDA3 expression in human superoxide dismutase 1-mutant amyotrophic lateral sclerosis astrocytes protects against neurotoxicity
Szebényi K et al. Inhibition of PHLDA3 expression in human superoxide dismutase 1-mutant amyotrophic lateral sclerosis astrocytes protects against neurotoxicity. . 2024-00-00. Pubmed ID: 39144751; DOI: 10.1093/braincomms/fcae244; PMC: PMC11323778 WTSIi097-A 2024-00-00 2024-00-00 PubMed: 39144751 DOI: 10.1093/braincomms/fcae244Associated cell lines:
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Reumann D, Krauditsch C, Novatchkova M, Sozzi E, Wong SN, Zabolocki M, Priouret M, Doleschall B, Ritzau-Reid KI, Piber M, Morassut I, Fieseler C, Fiorenzano A, Stevens MM, Zimmer M, Bardy C, Parmar M, Knoblich JA
In vitro modeling of the human dopaminergic system using spatially arranged ventral midbrain-striatum-cortex assembloids
Reumann D et al. In vitro modeling of the human dopaminergic system using spatially arranged ventral midbrain-striatum-cortex assembloids. . 2023-12-00. Pubmed ID: 38052989; DOI: 10.1038/s41592-023-02080-x; PMC: PMC10703680 WAe001-AIMBAi001-AIMBAi002-AIMBAi003-A 2023-12-00 2023-12-00 PubMed: 38052989 DOI: 10.1038/s41592-023-02080-xAssociated cell lines:
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Lee J, Duperrex E, El-Battrawy I, Hohn A, Saguner AM, Duru F, Emmenegger V, Cyganek L, Hierlemann A, Ulusan H
CardioMEA: comprehensive data analysis platform for studying cardiac diseases and drug responses
Lee J et al. CardioMEA: comprehensive data analysis platform for studying cardiac diseases and drug responses. . 2024-00-00. Pubmed ID: 39539954; DOI: 10.3389/fphys.2024.1472126; PMC: PMC11557525 UMGi129-AUMGi129-A-1 2024-00-00 2024-00-00 PubMed: 39539954 DOI: 10.3389/fphys.2024.1472126Associated cell lines:
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Lange T, Bach SM, Koppe TM, Klann A, Weise A, Alexander Pilz R, Loth N, Rheinbaben SV, Stracke S, Endlich N
Generation of a human induced pluripotent stem cell line (UMGACBi001-A) from urine cells of a chronic kidney disease patient with hypertension, diabetic nephropathy and acute sepsis
Lange T et al. Generation of a human induced pluripotent stem cell line (UMGACBi001-A) from urine cells of a chronic kidney disease patient with hypertension, diabetic nephropathy and acute sepsis. . 2023-12-00. Pubmed ID: 38323759; DOI: 10.1016/j.scr.2023.103224 SMBCi017-AUMGACBi001-A 2023-12-00 2023-12-00 PubMed: 38323759 DOI: 10.1016/j.scr.2023.103224Associated cell lines:
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Singh S, Plotnikova L, Karvonen K, Ryytty S, Hyppönen J, Kälviäinen R, Hämäläinen RH
Generation of a human induced pluripotent stem cell line (UEFi004-A) from a patient with progressive myoclonic epilepsy type 1 (EPM1)
Singh S et al. Generation of a human induced pluripotent stem cell line (UEFi004-A) from a patient with progressive myoclonic epilepsy type 1 (EPM1). . 2023-12-00. Pubmed ID: 37951142; DOI: 10.1016/j.scr.2023.103248 UEFi004-A 2023-12-00 2023-12-00 PubMed: 37951142 DOI: 10.1016/j.scr.2023.103248Associated cell lines:
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Huang Jie, Xie Yongpeng, Chen Bing, Xia Yu, Jiang Yanjiao, Sun Zengxian, Liu Yun
GPR146 regulates pulmonary vascular remodeling by promoting pulmonary artery smooth muscle cell proliferation through 5-lipoxygenase
Huang Jie et al. GPR146 regulates pulmonary vascular remodeling by promoting pulmonary artery smooth muscle cell proliferation through 5-lipoxygenase. . 2023-12-00. DOI: 10.1016/j.ejphar.2023.176123 ITXi001-AITXi001-A-1 2023-12-00 2023-12-00 DOI: 10.1016/j.ejphar.2023.176123Associated cell lines:
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Pavan C, Jin J, Jong S, Strbenac D, Davis RL, Sue CM, Johnston J, Lynch T, Halliday G, Kirik D, Parish CL, Thompson LH, Ovchinnikov DA
Generation of the iPSC line FINi002-A from a male Parkinson's disease patient carrying compound heterozygous mutations in the PRKN gene
Pavan C et al. Generation of the iPSC line FINi002-A from a male Parkinson's disease patient carrying compound heterozygous mutations in the PRKN gene. . 2023-12-00. Pubmed ID: 37890334; DOI: 10.1016/j.scr.2023.103211 FINi001-AFINi002-A 2023-12-00 2023-12-00 PubMed: 37890334 DOI: 10.1016/j.scr.2023.103211 -
Tong-Ngam P, Wongkummool W, Pongpaksupasin P, Rawara N, Kovanich D, Kitiyanant N, Munkongdee T, Paiboonsukwong K, Fucharoen S, Tubsuwan A
Generation of human induced pluripotent stem cell line (MUi033-A) from a male with homozygous for Hemoglobin E
Tong-Ngam P et al. Generation of human induced pluripotent stem cell line (MUi033-A) from a male with homozygous for Hemoglobin E. . 2023-12-00. Pubmed ID: 37890329; DOI: 10.1016/j.scr.2023.103228 MUi031-AMUi032-AMUi033-A 2023-12-00 2023-12-00 PubMed: 37890329 DOI: 10.1016/j.scr.2023.103228 -
Chen L, Chen G, Zhang M, Zhang X
Modeling sporadic juvenile ALS in iPSC-derived motor neurons explores the pathogenesis of FUS(R503fs) mutation
Chen L et al. Modeling sporadic juvenile ALS in iPSC-derived motor neurons explores the pathogenesis of FUS(R503fs) mutation. . 2024-00-00. Pubmed ID: 38711616; DOI: 10.3389/fncel.2024.1364164; PMC: PMC11070534 ZZUNEUi010-A 2024-00-00 2024-00-00 PubMed: 38711616 DOI: 10.3389/fncel.2024.1364164Associated cell lines:
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Tonin R, Feo F, Falliano S, Ferri L, Giunti L, Calamai M, Procopio E, Mari F, Conti V, Fanelli I, Bambi F, Guerrini R, Morrone A
Generation of human induced pluripotent stem cell line (AOUMEYi001-A) from a patient affected by Congenital disorders of glycosylation (ALG8-CDG) using self-replicating RNA vector
Tonin R et al. Generation of human induced pluripotent stem cell line (AOUMEYi001-A) from a patient affected by Congenital disorders of glycosylation (ALG8-CDG) using self-replicating RNA vector. . 2023-12-00. Pubmed ID: 38323760; DOI: 10.1016/j.scr.2023.103235 AOUMEYi001-A 2023-12-00 2023-12-00 PubMed: 38323760 DOI: 10.1016/j.scr.2023.103235Associated cell lines:
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Sirko S, Schichor C, Della Vecchia P, Metzger F, Sonsalla G, Simon T, Bürkle M, Kalpazidou S, Ninkovic J, Masserdotti G, Sauniere JF, Iacobelli V, Iacobelli S, Delbridge C, Hauck SM, Tonn JC, Götz M
Injury-specific factors in the cerebrospinal fluid regulate astrocyte plasticity in the human brain
Sirko S et al. Injury-specific factors in the cerebrospinal fluid regulate astrocyte plasticity in the human brain. . 2023-12-00. Pubmed ID: 38066208; DOI: 10.1038/s41591-023-02644-6; PMC: PMC10719094 UKERi006-AISFi001-A 2023-12-00 2023-12-00 PubMed: 38066208 DOI: 10.1038/s41591-023-02644-6Associated cell lines:
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Peng YH, Hsiao SK, Gupta K, Ruland A, Auernhammer GK, Maitz MF, Boye S, Lattner J, Gerri C, Honigmann A, Werner C, Krieg E
Dynamic matrices with DNA-encoded viscoelasticity for cell and organoid culture
Peng YH et al. Dynamic matrices with DNA-encoded viscoelasticity for cell and organoid culture. . 2023-12-00. Pubmed ID: 37550574; DOI: 10.1038/s41565-023-01483-3; PMC: PMC10716043 CRTDi003-B 2023-12-00 2023-12-00 PubMed: 37550574 DOI: 10.1038/s41565-023-01483-3Associated cell lines:
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Yang X, Zhang H, Gao M, Lv Y, Song W, Duan C, Liu Y
An induced pluripotent stem cell line (SDQLCHi062-A) from a patient carrying a mutation in the PAX2 gene
Yang X et al. An induced pluripotent stem cell line (SDQLCHi062-A) from a patient carrying a mutation in the PAX2 gene. . 2023-12-00. Pubmed ID: 38029557; DOI: 10.1016/j.scr.2023.103260 SDQLCHi062-A 2023-12-00 2023-12-00 PubMed: 38029557 DOI: 10.1016/j.scr.2023.103260Associated cell lines:
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Suárez-Herrera N, Leijsten N, Albert S, Bax NM, Hoyng CB, Cremers FPM, Garanto A, Collin RWJ
Generation of an iPSC line (RMCGENi020-A) from a patient with Stargardt disease harboring the recurrent intronic ABCA4 variant c.4253+43G>A
Suárez-Herrera N et al. Generation of an iPSC line (RMCGENi020-A) from a patient with Stargardt disease harboring the recurrent intronic ABCA4 variant c.4253+43G>A. . 2023-12-00. Pubmed ID: 37979432; DOI: 10.1016/j.scr.2023.103252 RMCGENi020-A 2023-12-00 2023-12-00 PubMed: 37979432 DOI: 10.1016/j.scr.2023.103252Associated cell lines:
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Denman CR, Tran HD, Shin MK, Ryu J, Kuhn B, Jo J
Generation of a human embryonic stem cell reporter line, TMEM119-EGFP, for the visualisation of in vitro differentiated human microglia
Denman CR et al. Generation of a human embryonic stem cell reporter line, TMEM119-EGFP, for the visualisation of in vitro differentiated human microglia. . 2023-12-00. Pubmed ID: 38029556; DOI: 10.1016/j.scr.2023.103264 WAe009-A-D 2023-12-00 2023-12-00 PubMed: 38029556 DOI: 10.1016/j.scr.2023.103264Associated cell lines:
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Nurieva W, Ivanova E, Chehab S, Singh P, Reichlmeir M, Szuhai K, Auburger GWJ, Skarnes WC, Ivics Z
Generation of four gene-edited human induced pluripotent stem cell lines with mutations in the ATM gene to model Ataxia-Telangiectasia
Nurieva W et al. Generation of four gene-edited human induced pluripotent stem cell lines with mutations in the ATM gene to model Ataxia-Telangiectasia. . 2023-12-00. Pubmed ID: 37976651; DOI: 10.1016/j.scr.2023.103247 WTSIi018-B-13WTSIi018-B-14WTSIi018-B-15WTSIi018-B-16 2023-12-00 2023-12-00 PubMed: 37976651 DOI: 10.1016/j.scr.2023.103247Associated cell lines:
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Zhao K, Zhang H, Cui J, Zhang Y, Zhou T, Long B
Generation of an NSD2-deficient human embryonic stem cell line using CRISPR/Cas9 technology
Zhao K et al. Generation of an NSD2-deficient human embryonic stem cell line using CRISPR/Cas9 technology. . 2023-12-00. Pubmed ID: 37992565; DOI: 10.1016/j.scr.2023.103255 WAe001-A-2B 2023-12-00 2023-12-00 PubMed: 37992565 DOI: 10.1016/j.scr.2023.103255Associated cell lines:
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Srivastava Abhay, Dhingra Sanjiv
iPSC-Based Disease Modeling and Functional Assessment of Neurons in Patients with Metabolic Disorder
Srivastava Abhay et al. iPSC-Based Disease Modeling and Functional Assessment of Neurons in Patients with Metabolic Disorder. . 2024-00-00. DOI: 10.1007/978-1-0716-3995-5_10 UOMi006-AUOMi008-A 2024-00-00 2024-00-00 DOI: 10.1007/978-1-0716-3995-5_10 -
Xu Ruodan, Gao Junwei, Cao Can, Shi Mingfei, Zhang Yonghui, Hong Shihao, Guo Shijie, Chen Menglin, Song Ping, Fu Gaoshuang, Li Jing, Liang Tengxiao, Miao Yingchun, Tang Lu, Yang Jinsheng, Li Ning, Dong Mingdong
HDL mimetics protect Alzheimer’s patients carrying APOE ε4 from SARS-CoV-2 invasion
Xu Ruodan et al. HDL mimetics protect Alzheimer’s patients carrying APOE ε4 from SARS-CoV-2 invasion. . 2023-12-00. DOI: 10.1016/j.nantod.2023.102051 IBTCMi001-AIBTCMi002-AIBTCMi004-AIBTCMi005-A 2023-12-00 2023-12-00 DOI: 10.1016/j.nantod.2023.102051Associated cell lines:
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Bax M, Junday K, Iismaa SE, Kaidonis X, Muller D, Hesselson S, Graham RM
Generation of induced pluripotent stem cell lines from a sister pair who suffered post-partum or recurrent Spontaneous Coronary Artery Dissections
Bax M et al. Generation of induced pluripotent stem cell lines from a sister pair who suffered post-partum or recurrent Spontaneous Coronary Artery Dissections. . 2023-12-00. Pubmed ID: 37939621; DOI: 10.1016/j.scr.2023.103238 UOWi005-AVCCRIi001-AVCCRIi002-AVCCRIi003-A 2023-12-00 2023-12-00 PubMed: 37939621 DOI: 10.1016/j.scr.2023.103238Associated cell lines:
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James E, Vielle A, Cusato K, Li H, Lee B, Parween S, Howell A, Johnson NR, Chial HJ, Potter H, Vergara MN
Human iPSC-derived retinal organoids develop robust Alzheimer's disease neuropathology
James E et al. Human iPSC-derived retinal organoids develop robust Alzheimer's disease neuropathology. . 2024-00-00. Pubmed ID: 38323188; DOI: 10.3389/fncel.2024.1340448; PMC: PMC10844524 HVRDi001-AHVRDi001-A-1 2024-00-00 2024-00-00 PubMed: 38323188 DOI: 10.3389/fncel.2024.1340448Associated cell lines:
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Luanpitpong S, Tangkiettrakul K, Kang X, Srisook P, Poohadsuan J, Samart P, Klaihmon P, Janan M, Lorthongpanich C, Laowtammathron C, Issaragrisil S
OGT and OGA gene-edited human induced pluripotent stem cells for dissecting the functional roles of O-GlcNAcylation in hematopoiesis
Luanpitpong S et al. OGT and OGA gene-edited human induced pluripotent stem cells for dissecting the functional roles of O-GlcNAcylation in hematopoiesis. . 2024-00-00. Pubmed ID: 38752196; DOI: 10.3389/fcell.2024.1361943; PMC: PMC11094211 MUSIi012-AMUSIi012-A-7MUSIi012-A-8 2024-00-00 2024-00-00 PubMed: 38752196 DOI: 10.3389/fcell.2024.1361943Associated cell lines:
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Astro Veronica, Adamo Antonio
Generation of iPSC Cell Lines from Patients with Sex Chromosome Aneuploidies
Astro Veronica et al. Generation of iPSC Cell Lines from Patients with Sex Chromosome Aneuploidies. . 2024-00-00. DOI: 10.1007/978-1-0716-3698-5_14 KAUSTi001-AKAUSTi003-AKAUSTi004-AKAUSTi004-BKAUSTi005-AKAUSTi005-BKAUSTi005-CKAUSTi001-BKAUSTi006-AKAUSTi006-BKAUSTi007-AKAUSTi008-AKAUSTi008-BKAUSTi008-CKAUSTi008-DKAUSTi008-EKAUSTi008-FKAUSTi008-GKAUSTi007-BKAUSTi009-AKAUSTi009-BKAUSTi010-AKAUSTi010-B 2024-00-00 2024-00-00 DOI: 10.1007/978-1-0716-3698-5_14 -
Gao C, Liu Y, Liu N, Li Z, Yang X, Yang Y, Xi Y, Tian J, Gai Z
Establishment of human induced pluripotent stem cell line (SDQLCHi060-A) from a patient with AUTS2 syndrome carrying a heterozygous mutation in AUTS2 gene
Gao C et al. Establishment of human induced pluripotent stem cell line (SDQLCHi060-A) from a patient with AUTS2 syndrome carrying a heterozygous mutation in AUTS2 gene. . 2023-12-00. Pubmed ID: 37948839; DOI: 10.1016/j.scr.2023.103242 SDQLCHi060-A 2023-12-00 2023-12-00 PubMed: 37948839 DOI: 10.1016/j.scr.2023.103242Associated cell lines:
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Lemarié Lucas, Sohier Jérôme, COURTIAL Edwin-Jeffroy
Exploring the Tunable Micro-/Macro-Structure Enabled by Alginate-Gelatin Bioinks for Tissue Engineering
Lemarié Lucas et al. Exploring the Tunable Micro-/Macro-Structure Enabled by Alginate-Gelatin Bioinks for Tissue Engineering. . 2024-00-00. DOI: 10.2139/ssrn.4816628 SCTi003-A 2024-00-00 2024-00-00 DOI: 10.2139/ssrn.4816628Associated cell lines:
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Kayser A, Dittmann S, van Impel A, Šarić T, Schulze-Bahr E
Patient-derived stem cell line UKMi005-A (hiPSC) harboring a non-synonymous heterozygous KCNJ5 gene variant
Kayser A et al. Patient-derived stem cell line UKMi005-A (hiPSC) harboring a non-synonymous heterozygous KCNJ5 gene variant. . 2023-12-00. Pubmed ID: 37890333; DOI: 10.1016/j.scr.2023.103223 UKMi005-A 2023-12-00 2023-12-00 PubMed: 37890333 DOI: 10.1016/j.scr.2023.103223Associated cell lines:
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Pham Vi, Sertori Finoti Livia, Cassidy Margaret M., Maguire Jean Ann, Gagne Alyssa L., Waxman Elisa A., French Deborah L., King Kaitlyn, Zhou Zitao, Gelb Michael H., Wongkittichote Parith, Hong Xinying, Schlotawa Lars, Davidson Beverly L., Ahrens-Nicklas Rebecca C.
A novel iPSC model reveals selective vulnerability of neurons in multiple sulfatase deficiency
Pham Vi et al. A novel iPSC model reveals selective vulnerability of neurons in multiple sulfatase deficiency. . 2023-12-00. DOI: 10.1016/j.ymgme.2023.108116 CHOPi002-ACHOPi003-A 2023-12-00 2023-12-00 DOI: 10.1016/j.ymgme.2023.108116Associated cell lines:
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Ludwik KA, Opitz R, Jyrch S, Megges M, Weiner J, Beule D, Kühnen P, Stachelscheid H
Generation of iPSC lines with SLC16A2:G401R or SLC16A2 knock out
Ludwik KA et al. Generation of iPSC lines with SLC16A2:G401R or SLC16A2 knock out. . 2023-12-00. Pubmed ID: 38006677; DOI: 10.1016/j.scr.2023.103256 BIHi001-BBIHi001-B-1BIHi001-B-7BIHi001-B-8 2023-12-00 2023-12-00 PubMed: 38006677 DOI: 10.1016/j.scr.2023.103256Associated cell lines:
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Paley E.L.
Tryptamine Microbiota-Deregulated Aminoacyl-tRNA Biosynthesis
Paley E.L.. Tryptamine Microbiota-Deregulated Aminoacyl-tRNA Biosynthesis. . 2024-00-00. DOI: 10.1016/c2023-0-50773-6 NSi001-ANSi001-BNSi001-C 2024-00-00 2024-00-00 DOI: 10.1016/c2023-0-50773-6 -
Mathias A, Perriot S, Jones S, Canales M, Bernard-Valnet R, Gimenez M, Torcida N, Oberholster L, Hottinger AF, Zekeridou A, Theaudin M, Pot C, Du Pasquier R
Human stem cell-derived neurons and astrocytes to detect novel auto-reactive IgG response in immune-mediated neurological diseases
Mathias A et al. Human stem cell-derived neurons and astrocytes to detect novel auto-reactive IgG response in immune-mediated neurological diseases. . 2024-00-00. Pubmed ID: 39114659; DOI: 10.3389/fimmu.2024.1419712; PMC: PMC11303155 LNISi002-BLNISi003-A 2024-00-00 2024-00-00 PubMed: 39114659 DOI: 10.3389/fimmu.2024.1419712Associated cell lines:
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Clua Provost C, Auboyer L, Rovelet-Lecrux A, Monzo C, Schob E, Andreux F, Quittet C, Lehmann S, Wallon D, Crozet C
Generation of induced pluripotent stem cell lines IRMBi003-A and IRMBi003-B from a healthy donor to model Alzheimer's disease
Clua Provost C et al. Generation of induced pluripotent stem cell lines IRMBi003-A and IRMBi003-B from a healthy donor to model Alzheimer's disease. . 2023-12-00. Pubmed ID: 37979430; DOI: 10.1016/j.scr.2023.103250 IRMBi001-AIRMBi002-AIRMBi003-AIRMBi003-B 2023-12-00 2023-12-00 PubMed: 37979430 DOI: 10.1016/j.scr.2023.103250Associated cell lines:
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Rodriguez Gonzalez C, Basílio-Queirós D, Neehus AL, Merkert S, Tschritter D, Ünal S, Hegermann J, Mörgelin M, Bustamante J, Nietert MM, Martin U, Tümmler B, Munder A, Lachmann N
Human CFTR deficient iPSC-macrophages reveal impaired functional and transcriptomic response upon Pseudomonas aeruginosa infection
Rodriguez Gonzalez C et al. Human CFTR deficient iPSC-macrophages reveal impaired functional and transcriptomic response upon Pseudomonas aeruginosa infection. . 2024-00-00. Pubmed ID: 39606224; DOI: 10.3389/fimmu.2024.1397886; PMC: PMC11601075 MHHi002-AMHHi005-AMHHi015-A 2024-00-00 2024-00-00 PubMed: 39606224 DOI: 10.3389/fimmu.2024.1397886 -
Sarieva K, Kagermeier T, Khakipoor S, Atay E, Yentür Z, Becker K, Mayer S
Human brain organoid model of maternal immune activation identifies radial glia cells as selectively vulnerable
Sarieva K et al. Human brain organoid model of maternal immune activation identifies radial glia cells as selectively vulnerable. . 2023-12-00. Pubmed ID: 36878967; DOI: 10.1038/s41380-023-01997-1; PMC: PMC9986664 BIONi010-CBIONi010-C-80 2023-12-00 2023-12-00 PubMed: 36878967 DOI: 10.1038/s41380-023-01997-1Associated cell lines:
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Ruan Y, Tian X, Li X, Zhang Y
Establishment of a human TLR4 compound heterozygous knockout hESC line (WAe009-A-N) to model toll-like receptor 4 deficiency by CRISPR/Cas9 system
Ruan Y et al. Establishment of a human TLR4 compound heterozygous knockout hESC line (WAe009-A-N) to model toll-like receptor 4 deficiency by CRISPR/Cas9 system. . 2023-12-00. Pubmed ID: 37931537; DOI: 10.1016/j.scr.2023.103225 WAe009-AWAe009-A-N 2023-12-00 2023-12-00 PubMed: 37931537 DOI: 10.1016/j.scr.2023.103225Associated cell lines:
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Meier AB, Zawada D, De Angelis MT, Martens LD, Santamaria G, Zengerle S, Nowak-Imialek M, Kornherr J, Zhang F, Tian Q, Wolf CM, Kupatt C, Sahara M, Lipp P, Theis FJ, Gagneur J, Goedel A, Laugwitz KL, Dorn T, Moretti A
Epicardioid single-cell genomics uncovers principles of human epicardium biology in heart development and disease
Meier AB et al. Epicardioid single-cell genomics uncovers principles of human epicardium biology in heart development and disease. . 2023-12-00. Pubmed ID: 37012447; DOI: 10.1038/s41587-023-01718-7; PMC: PMC10713454 MRIi001-AMRIi003-AMRIi025-AMRIi003-A-6MRIi003-A-9 2023-12-00 2023-12-00 PubMed: 37012447 DOI: 10.1038/s41587-023-01718-7Associated cell lines:
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Wang L, Zheng G, Wang P, Jia X
Unlocking the secrets of NPSLE: the role of dendritic cell-secreted CCL2 in blood-brain barrier disruption
Wang L et al. Unlocking the secrets of NPSLE: the role of dendritic cell-secreted CCL2 in blood-brain barrier disruption. . 2024-00-00. Pubmed ID: 39403387; DOI: 10.3389/fimmu.2024.1343805; PMC: PMC11472714 WISCi004-B 2024-00-00 2024-00-00 PubMed: 39403387 DOI: 10.3389/fimmu.2024.1343805Associated cell lines:
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Giacomoni J, Åkerblom M, Habekost M, Fiorenzano A, Kajtez J, Davidsson M, Parmar M, Björklund T
Identification and validation of novel engineered AAV capsid variants targeting human glia
Giacomoni J et al. Identification and validation of novel engineered AAV capsid variants targeting human glia. . 2024-00-00. Pubmed ID: 39193523; DOI: 10.3389/fnins.2024.1435212; PMC: PMC11348808 RCe021-A 2024-00-00 2024-00-00 PubMed: 39193523 DOI: 10.3389/fnins.2024.1435212Associated cell lines:
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Gargano C, Vartanian-Grimaldi JS, Hovhannisyan Y, Joanne P, Agbulut O, Li Z, Parlakian A, Decaux JF
Generation of induced pluripotent stem cell line (TMOi001-A-11) carrying a homozygous deletion in the synemin gene using CRISPR/Cas9
Gargano C et al. Generation of induced pluripotent stem cell line (TMOi001-A-11) carrying a homozygous deletion in the synemin gene using CRISPR/Cas9. . 2023-12-00. Pubmed ID: 38035530; DOI: 10.1016/j.scr.2023.103254 TMOi001-ATMOi001-A-11 2023-12-00 2023-12-00 PubMed: 38035530 DOI: 10.1016/j.scr.2023.103254Associated cell lines:
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Kondrateva E, Grigorieva O, Panchuk I, Bychkov I, Zakharova E, Tabakov V, Pozhitnova V, Voronina E, Shchagina O, Lavrov A, Smirnikhina S, Kutsev S
Generation of induced pluripotent stem cell line (RCMGi012-A) from fibroblasts of patient with mucopolysaccharidosis type VI
Kondrateva E et al. Generation of induced pluripotent stem cell line (RCMGi012-A) from fibroblasts of patient with mucopolysaccharidosis type VI. . 2023-12-00. Pubmed ID: 38006675; DOI: 10.1016/j.scr.2023.103259 RCMGi012-A 2023-12-00 2023-12-00 PubMed: 38006675 DOI: 10.1016/j.scr.2023.103259Associated cell lines:
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Schmidt Clara, Deyett Alison, Ilmer Tobias, Haendeler Simon, Torres Caballero Aranxa, Novatchkova Maria, Netzer Michael A., Ceci Ginistrelli Lavinia, Mancheno Juncosa Estela, Bhattacharya Tanishta, Mujadzic Amra, Pimpale Lokesh, Jahnel Stefan M., Cirigliano Martina, Reumann Daniel, Tavernini Katherina, Papai Nora, Hering Steffen, Hofbauer Pablo, Mendjan Sasha
Multi-chamber cardioids unravel human heart development and cardiac defects
Schmidt Clara et al. Multi-chamber cardioids unravel human heart development and cardiac defects. . 2023-12-00. DOI: 10.1016/j.cell.2023.10.030 IMBAi003-A 2023-12-00 2023-12-00 DOI: 10.1016/j.cell.2023.10.030Associated cell lines:
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Wang QH, Liu LY, Wang YY, He W, Wang J, Wang J, Zou LP
Generation and characterization of induced pluripotent stem cell lines derived from skin fibroblasts of patients with adrenoleukodystrophy
Wang QH et al. Generation and characterization of induced pluripotent stem cell lines derived from skin fibroblasts of patients with adrenoleukodystrophy. . 2023-12-00. Pubmed ID: 37948838; DOI: 10.1016/j.scr.2023.103243 MSCPi001-AMSCPi002-A 2023-12-00 2023-12-00 PubMed: 37948838 DOI: 10.1016/j.scr.2023.103243Associated cell lines:
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Zhang M, Venkateshappa R, Li A, Fowler MB, Telli ML, Wu JC
Generation and characterization of induced pluripotent stem cells from breast cancer patients carrying ATM mutations
Zhang M et al. Generation and characterization of induced pluripotent stem cells from breast cancer patients carrying ATM mutations. . 2023-12-00. Pubmed ID: 37951143; DOI: 10.1016/j.scr.2023.103246; PMC: PMC10789563 SCVIi083-ASCVIi084-A 2023-12-00 2023-12-00 PubMed: 37951143 DOI: 10.1016/j.scr.2023.103246Associated cell lines:
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Yuan L, Wang Y, Xie R, Lin D, Wang X
Generation and characterization of iPS cell line (SYSUSHi002-A) from PBMCs of an AML patient with TP53 mutation
Yuan L et al. Generation and characterization of iPS cell line (SYSUSHi002-A) from PBMCs of an AML patient with TP53 mutation. . 2023-12-00. Pubmed ID: 37890328; DOI: 10.1016/j.scr.2023.103230 SYSUSHi002-A 2023-12-00 2023-12-00 PubMed: 37890328 DOI: 10.1016/j.scr.2023.103230Associated cell lines:
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Driver K, Vo C, Scriba CK, Saker S, Larmonier T, Malfatti E, Romero NB, Ravenscroft G, Laing NG, Taylor RL, Clayton JS
Generation of two induced pluripotent stem cell lines from a 33-year-old central core disease patient with a heterozygous dominant c.14145_14156delCTACTGGGACA (p.Asn4715_Asp4718del) deletion in the RYR1 gene
Driver K et al. Generation of two induced pluripotent stem cell lines from a 33-year-old central core disease patient with a heterozygous dominant c.14145_14156delCTACTGGGACA (p.Asn4715_Asp4718del) deletion in the RYR1 gene. . 2023-12-00. Pubmed ID: 38029555; DOI: 10.1016/j.scr.2023.103258 HPIi005-AHPIi005-B 2023-12-00 2023-12-00 PubMed: 38029555 DOI: 10.1016/j.scr.2023.103258 -
Chen Yuzhuo, Yang Zhirong, He Xingqiang, Zhu Wanglong, Wang Yujun, Li Jiaofeng, Han Zhengyu, Wen Jie, Liu Wei, Yang Yuhan, Zhang Kun
Proanthocyanidins inhibited colorectal cancer stem cell characteristics through Wnt/β‐catenin signaling
Chen Yuzhuo et al. Proanthocyanidins inhibited colorectal cancer stem cell characteristics through Wnt/β‐catenin signaling. . 2023-12-00. DOI: 10.1002/tox.23924 UJSi002-A 2023-12-00 2023-12-00 DOI: 10.1002/tox.23924Associated cell lines:
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McDiarmid AH, Gospodinova KO, Elliott RJR, Dawson JC, Graham RE, El-Daher MT, Anderson SM, Glen SC, Glerup S, Carragher NO, Evans KL
Morphological profiling in human neural progenitor cells classifies hits in a pilot drug screen for Alzheimer's disease
McDiarmid AH et al. Morphological profiling in human neural progenitor cells classifies hits in a pilot drug screen for Alzheimer's disease. . 2024-00-00. Pubmed ID: 38576795; DOI: 10.1093/braincomms/fcae101; PMC: PMC10994270 WTSIi004-B 2024-00-00 2024-00-00 PubMed: 38576795 DOI: 10.1093/braincomms/fcae101Associated cell lines:
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Martínez-Moreno R, Pérez-Serra A, Selga E, Carreras D, Aran B, Kuebler B, Scornik FS, Pérez GJ, Brugada R
Generation of the induced pluripotent stem cell line ESi108-A from a familial atrial fibrillation patient
Martínez-Moreno R et al. Generation of the induced pluripotent stem cell line ESi108-A from a familial atrial fibrillation patient. . 2023-12-00. Pubmed ID: 37922745; DOI: 10.1016/j.scr.2023.103239 ESi108-A 2023-12-00 2023-12-00 PubMed: 37922745 DOI: 10.1016/j.scr.2023.103239Associated cell lines:
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Gabbin B, Meraviglia V, Angenent ML, Ward-van Oostwaard D, Sol W, Mummery CL, Rabelink TJ, van Meer BJ, van den Berg CW, Bellin M
Heart and kidney organoids maintain organ-specific function in a microfluidic system
Gabbin B et al. Heart and kidney organoids maintain organ-specific function in a microfluidic system. . 2023-12-00. Pubmed ID: 37810749; DOI: 10.1016/j.mtbio.2023.100818; PMC: PMC10550812 LUMCi028-ALUMCi029-A 2023-12-00 2023-12-00 PubMed: 37810749 DOI: 10.1016/j.mtbio.2023.100818Associated cell lines:
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Xu Q, Zhang X, Hao M, Dang X, Xu Q, Cyganek L, Akin I, Tang D, Liao B, Zhou X, Lan H
Esophageal Cancer-Related Gene-4 Contributes to Lipopolysaccharide-Induced Ion Channel Dysfunction in hiPSC-Derived Cardiomyocytes
Xu Q et al. Esophageal Cancer-Related Gene-4 Contributes to Lipopolysaccharide-Induced Ion Channel Dysfunction in hiPSC-Derived Cardiomyocytes. . 2024-00-00. Pubmed ID: 39649417; DOI: 10.2147/jir.s470828; PMC: PMC11624686 UMGi014-B 2024-00-00 2024-00-00 PubMed: 39649417 DOI: 10.2147/jir.s470828Associated cell lines:
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Mao S, Sun X, Duan C, Jiang B, Ma H, Ji S, Liang Y, Zhang R, Chen J, Tang S
Generation of a gene-corrected isogenic iPSC cell line from an X-linked retinoschisis patient with a hemizygous mutation c.304C > T (p.R102W) in RS1 gene
Mao S et al. Generation of a gene-corrected isogenic iPSC cell line from an X-linked retinoschisis patient with a hemizygous mutation c.304C > T (p.R102W) in RS1 gene. . 2023-12-00. Pubmed ID: 38011758; DOI: 10.1016/j.scr.2023.103263 CSUASOi001-ACSUASOi005-ACSUASOi001-A-1 2023-12-00 2023-12-00 PubMed: 38011758 DOI: 10.1016/j.scr.2023.103263Associated cell lines:
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Kangboonruang K, Pornsukjantra T, Tong-Ngam P, Chokpanuwat T, Tim-Aroon T, Wattanasirichaigoon D, Anurathapan U, Hongeng S, Asavapanumas N, Bhukhai K, Tubsuwan A
Establishment of MUi030-A: A human induced pluripotent stem cell line carrying homozygous L444P mutation in the GBA1 gene to study type-3 Gaucher disease
Kangboonruang K et al. Establishment of MUi030-A: A human induced pluripotent stem cell line carrying homozygous L444P mutation in the GBA1 gene to study type-3 Gaucher disease. . 2023-12-00. Pubmed ID: 37890332; DOI: 10.1016/j.scr.2023.103229 MUi030-AMUi032-A 2023-12-00 2023-12-00 PubMed: 37890332 DOI: 10.1016/j.scr.2023.103229 -
Zhang F, Chen S, Chen Y, Chen X, Cen Z, Luo W
Generation of an induced pluripotent stem cell line (ZJUi013-A) from a Familial cortical myoclonic tremor with epilepsy type 1 patient carrying (TTTCA)(n) insertion in the SAMD12 gene
Zhang F et al. Generation of an induced pluripotent stem cell line (ZJUi013-A) from a Familial cortical myoclonic tremor with epilepsy type 1 patient carrying (TTTCA)(n) insertion in the SAMD12 gene. . 2023-12-00. Pubmed ID: 37890330; DOI: 10.1016/j.scr.2023.103236 ZJUi013-A 2023-12-00 2023-12-00 PubMed: 37890330 DOI: 10.1016/j.scr.2023.103236Associated cell lines:
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Rhode J, Hagenau L, Beimdiek J, Ullmann R, Hossain F, Tzvetkova A, Jensen LR, Kuss AW
Generation of two iPSC lines (MHHi001-A-12 and MHHi001-A-13) carrying biallelic truncating mutations at the 3'-end of SRCAP using CRISPR/Cas9
Rhode J et al. Generation of two iPSC lines (MHHi001-A-12 and MHHi001-A-13) carrying biallelic truncating mutations at the 3'-end of SRCAP using CRISPR/Cas9. . 2023-12-00. Pubmed ID: 38006676; DOI: 10.1016/j.scr.2023.103249 MHHi001-AMHHi001-A-12MHHi001-A-13 2023-12-00 2023-12-00 PubMed: 38006676 DOI: 10.1016/j.scr.2023.103249Associated cell lines:
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Khomyakova E. A., Fedorenko A. V., Surdina A. V., Volovikov E. A., Belikova L. D., Zerkalenkova E. A., Lagarkova M. A., Bogomazova A. N.
Derivation of Induced Pluripotent Stem Cells Line (RCPCMi009-A-1) with Knockout of the UBE2A Gene Using CRISPR/Cas9 Genome Editing
Khomyakova E. A. et al. Derivation of Induced Pluripotent Stem Cells Line (RCPCMi009-A-1) with Knockout of the UBE2A Gene Using CRISPR/Cas9 Genome Editing. . 2023-12-00. DOI: 10.1134/s1062360423060048 RCPCMi009-ARCPCMi009-A-1 2023-12-00 2023-12-00 DOI: 10.1134/s1062360423060048Associated cell lines:
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Dev E, Adamska P, Wolnik J, Oleksy A, Piętowska Z, Zalewski A, Maj J, Dulak J, Biniecka M
Generation of two induced pluripotent stem cell lines from psoriatic patient with cardiovascular comorbidity
Dev E et al. Generation of two induced pluripotent stem cell lines from psoriatic patient with cardiovascular comorbidity. . 2023-12-00. Pubmed ID: 37979431; DOI: 10.1016/j.scr.2023.103251 IMEDEAi007-ADMBi007-ADMBi008-A 2023-12-00 2023-12-00 PubMed: 37979431 DOI: 10.1016/j.scr.2023.103251Associated cell lines:
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Wang T, Hou S, Chen J, Zhao X, Xiao T, Hou C, Zhou C
Generation of an induced pluripotent stem cell line (SHETi004-A) from a Chinese Han child with left bundle branch block
Wang T et al. Generation of an induced pluripotent stem cell line (SHETi004-A) from a Chinese Han child with left bundle branch block. . 2023-12-00. Pubmed ID: 37931536; DOI: 10.1016/j.scr.2023.103227 SHETi004-A 2023-12-00 2023-12-00 PubMed: 37931536 DOI: 10.1016/j.scr.2023.103227Associated cell lines:
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Huang Xiaokai, Xu Chengwu, Dai Haipeng, Yang Jianchun, Huang Tingting, Chen Shuan, Qi Lingxin, Ruan Jichen, Wang Juxiang
NCDN is a Potential Biomarker and Therapeutic Target for Glioblastoma
Huang Xiaokai et al. NCDN is a Potential Biomarker and Therapeutic Target for Glioblastoma. . 2024-00-00. DOI: 10.7150/jca.90535 KICRi002-AKICRi002-A-3 2024-00-00 2024-00-00 DOI: 10.7150/jca.90535Associated cell lines:
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Kuczynska Zuzanna, Neglur Pawan Kumar, Metin Erkan, Liput Michal, Zychowicz Marzena, Zayat Valery, Krześniak Natalia E., Buzanska Leonora, Kot Marta
Safety of GMP-compliant iPSC lines generated by Sendai virus transduction is dependent upon clone identity and sex of the donor
Kuczynska Zuzanna et al. Safety of GMP-compliant iPSC lines generated by Sendai virus transduction is dependent upon clone identity and sex of the donor. . 2024-00-00. DOI: 10.5114/fn.2024.134026 KUMi002-AKUMi003-A 2024-00-00 2024-00-00 DOI: 10.5114/fn.2024.134026 -
Noack F, Vangelisti S, Ditzer N, Chong F, Albert M, Bonev B
Joint epigenome profiling reveals cell-type-specific gene regulatory programmes in human cortical organoids
Noack F et al. Joint epigenome profiling reveals cell-type-specific gene regulatory programmes in human cortical organoids. . 2023-12-00. Pubmed ID: 37996647; DOI: 10.1038/s41556-023-01296-5; PMC: PMC10709149 CRTDi004-AISFi001-A 2023-12-00 2023-12-00 PubMed: 37996647 DOI: 10.1038/s41556-023-01296-5Associated cell lines:
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Jang Deasung, Matthews Kerryn, Deng Pan, Berryman Samuel G., Nian Cuilan, Duffy Simon P., Lynn Francis C., Ma Hongshen
Single cell glucose-stimulated insulin secretion assay using nanowell-in-microwell plates
Jang Deasung et al. Single cell glucose-stimulated insulin secretion assay using nanowell-in-microwell plates. . 2024-00-00. DOI: 10.1039/d4lc00413b HMGUi001-AHMGUi001-A-8 2024-00-00 2024-00-00 DOI: 10.1039/d4lc00413bAssociated cell lines:
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Pollock Samuel D., Galicia-Silva Israeli M., Liu Mai, Gruskin Zoe L., Alvarez-Dominguez Juan R.
Scalable generation of 3D pancreatic islet organoids from human pluripotent stem cells in suspension bioreactors
Pollock Samuel D. et al. Scalable generation of 3D pancreatic islet organoids from human pluripotent stem cells in suspension bioreactors. . 2023-12-00. DOI: 10.1016/j.xpro.2023.102580 SCSe001-ASCSe001-A-3 2023-12-00 2023-12-00 DOI: 10.1016/j.xpro.2023.102580Associated cell lines:
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Hatim O, Pavlinov I, Xu M, Linask K, Beers J, Liu C, Baumgärtel K, Gilbert M, Spinner N, Chen C, Zou J, Zheng W
Generation of an Alagille syndrome (ALGS) patient-derived induced pluripotent stem cell line (TRNDi032-A) carrying a heterozygous mutation (p.Cys682Leufs*7) in the JAG1 gene
Hatim O et al. Generation of an Alagille syndrome (ALGS) patient-derived induced pluripotent stem cell line (TRNDi032-A) carrying a heterozygous mutation (p.Cys682Leufs*7) in the JAG1 gene. . 2023-12-00. Pubmed ID: 37890331; DOI: 10.1016/j.scr.2023.103231; PMC: PMC10842201 TRNDi032-A 2023-12-00 2023-12-00 PubMed: 37890331 DOI: 10.1016/j.scr.2023.103231Associated cell lines:
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Yang X, Yu C, Gao M, Liu Y, Liu Y
Generation of an induced pluripotent stem cell (iPSC) line SDQLCHi056-A from a patient with Nicolaides-Baraitser syndrome carrying a mutation in SMARCA2 gene
Yang X et al. Generation of an induced pluripotent stem cell (iPSC) line SDQLCHi056-A from a patient with Nicolaides-Baraitser syndrome carrying a mutation in SMARCA2 gene. . 2023-12-00. Pubmed ID: 37995436; DOI: 10.1016/j.scr.2023.103244 SDQLCHi056-A 2023-12-00 2023-12-00 PubMed: 37995436 DOI: 10.1016/j.scr.2023.103244Associated cell lines:
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Yang Yi-Can, Tang Qiong, Yan Li-Juan, Zhang Shi-Bin, Ye Xiao-Min, Gong Dai, Zou Li, Wen Xiang-Lan
A Case of Floating-Harbor Syndrome with “Growth and Language Development Delay” as Its Clinical Manifestation
Yang Yi-Can et al. A Case of Floating-Harbor Syndrome with “Growth and Language Development Delay” as Its Clinical Manifestation. . 2023-12-00. DOI: 10.2147/pgpm.s433444 UMGWi001-B 2023-12-00 2023-12-00 DOI: 10.2147/pgpm.s433444Associated cell lines:
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Dementyeva E. V., Klimenko E. S., Minina J. M., Zakian S. M., Kostareva A. A.
Generation of an Induced Pluripotent Stem Cell Line ICGi046-A of a Patient Carrying Pathogenic p.Ser259Thr Variant in RAF1 Associated with RASopathy
Dementyeva E. V. et al. Generation of an Induced Pluripotent Stem Cell Line ICGi046-A of a Patient Carrying Pathogenic p.Ser259Thr Variant in RAF1 Associated with RASopathy. . 2023-12-00. DOI: 10.1134/s1062360423070032 ICGi046-A 2023-12-00 2023-12-00 DOI: 10.1134/s1062360423070032Associated cell lines:
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Harancher MR, Sukhwani M, Castro CA, Hsieh MH, Orwig KE
Generation of two isogenic sickle cell disease induced pluripotent stem cell lines from testicular fibroblasts
Harancher MR et al. Generation of two isogenic sickle cell disease induced pluripotent stem cell lines from testicular fibroblasts. . 2023-12-00. Pubmed ID: 38000347; DOI: 10.1016/j.scr.2023.103257; PMC: PMC10845156 UPITTi004-AUPITTi004-B 2023-12-00 2023-12-00 PubMed: 38000347 DOI: 10.1016/j.scr.2023.103257Associated cell lines:
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Chehelgerdi Matin, Behdarvand Dehkordi Fereshteh, Chehelgerdi Mohammad, Kabiri Hamidreza, Salehian-Dehkordi Hosein, Abdolvand Mohammad, Salmanizadeh Sharareh, Rashidi Mohsen, Niazmand Anoosha, Ahmadi Saba, Feizbakhshan Sara, Kabiri Saber, Vatandoost Nasimeh, Ranjbarnejad Tayebeh
Exploring the promising potential of induced pluripotent stem cells in cancer research and therapy
Chehelgerdi Matin et al. Exploring the promising potential of induced pluripotent stem cells in cancer research and therapy. . 2023-11-28. DOI: 10.1186/s12943-023-01873-0 KUMCi002-AKUMi004-AKUMi005-A 2023-11-28 2023-11-28 DOI: 10.1186/s12943-023-01873-0Associated cell lines:
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Klaihmon P, Luanpitpong S, Kang X, Issaragrisil S
Anti-TIM3 chimeric antigen receptor-natural killer cells from engineered induced pluripotent stem cells effectively target acute myeloid leukemia cells
Klaihmon P et al. Anti-TIM3 chimeric antigen receptor-natural killer cells from engineered induced pluripotent stem cells effectively target acute myeloid leukemia cells. . 2023-11-27. Pubmed ID: 38012684; DOI: 10.1186/s12935-023-03153-9; PMC: PMC10680184 MUSIi013-AMUSIi013-A-2 2023-11-27 2023-11-27 PubMed: 38012684 DOI: 10.1186/s12935-023-03153-9Associated cell lines:
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Liang Yuqin, Sun Xihao, Duan Chunwen, Tang Shibo, Chen Jiansu
Application of patient-derived induced pluripotent stem cells and organoids in inherited retinal diseases
Liang Yuqin et al. Application of patient-derived induced pluripotent stem cells and organoids in inherited retinal diseases. . 2023-11-27. DOI: 10.1186/s13287-023-03564-5 FRIMOi002-AINMi004-AFRIMOi005-ACSUASOi001-AZOCi001-ACSUASOi003-ACSUASOi004-ACSUASOi005-AUCLi014-AUCLi015-ACSUASOi006-AZOCi002-AZOCi004-APUMCHi018-A 2023-11-27 2023-11-27 DOI: 10.1186/s13287-023-03564-5 -
Adegunsoye Ayodeji, Gonzales Natalia M., Gilad Yoav
Induced Pluripotent Stem Cells in Disease Biology and the Evidence for Their In Vitro Utility
Adegunsoye Ayodeji et al. Induced Pluripotent Stem Cells in Disease Biology and the Evidence for Their In Vitro Utility. . 2023-11-27. DOI: 10.1146/annurev-genet-022123-090319 FDCHi004-A 2023-11-27 2023-11-27 DOI: 10.1146/annurev-genet-022123-090319Associated cell lines:
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Shnaider Tatiana A., Khabarova Anna A., Morozova Ksenia N., Yunusova Anastasia M., Yakovleva Sophia A., Chvileva Anastasia S., Wolf Ekaterina R., Kiseleva Elena V., Grigor’eva Elena V., Voinova Viktori Y., Lagarkova Maria A., Pomerantseva Ekaterina A., Musatova Elizaveta V., Smirnov Alexander V., Smirnova Anna V., Stoklitskaya Diana S., Arefieva Tatiana I., Larina Daria A., Nikitina Tatiana V., Pristyazhnyuk Inna E.
Ultrastructural Abnormalities in Induced Pluripotent Stem Cell-Derived Neural Stem Cells and Neurons of Two Cohen Syndrome Patients
Shnaider Tatiana A. et al. Ultrastructural Abnormalities in Induced Pluripotent Stem Cell-Derived Neural Stem Cells and Neurons of Two Cohen Syndrome Patients. . 2023-11-25. DOI: 10.3390/cells12232702 ICGi034-A 2023-11-25 2023-11-25 DOI: 10.3390/cells12232702Associated cell lines:
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Bu Q, Dai Y, Zhang H, Li M, Liu H, Huang Y, Zeng A, Qin F, Jiang L, Wang L, Chen Y, Li H, Wang X, Zhao Y, Qin M, Zhao Y, Zhang N, Kuang W, Zhao Y, Cen X
Neurodevelopmental defects in human cortical organoids with N-acetylneuraminic acid synthase mutation
Bu Q et al. Neurodevelopmental defects in human cortical organoids with N-acetylneuraminic acid synthase mutation. . 2023-11-24. Pubmed ID: 38000033; DOI: 10.1126/sciadv.adf2772; PMC: PMC10672180 NCCSEDi001-ANCCSEDi001-A-1 2023-11-24 2023-11-24 PubMed: 38000033 DOI: 10.1126/sciadv.adf2772Associated cell lines:
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Chapotte-Baldacci CA, Pierre M, Djemai M, Pouliot V, Chahine M
Biophysical properties of Na(V)1.5 channels from atrial-like and ventricular-like cardiomyocytes derived from human induced pluripotent stem cells
Chapotte-Baldacci CA et al. Biophysical properties of Na(V)1.5 channels from atrial-like and ventricular-like cardiomyocytes derived from human induced pluripotent stem cells. . 2023-11-24. Pubmed ID: 38001331; DOI: 10.1038/s41598-023-47310-6; PMC: PMC10673932 CBRCULi001-ACBRCULi002-ACBRCULi003-ACBRCULi004-ACBRCULi005-ACBRCULi008-ACBRCULi009-A 2023-11-24 2023-11-24 PubMed: 38001331 DOI: 10.1038/s41598-023-47310-6Associated cell lines:
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Gong Yiming, Chen Qiuju, He Xiaolong, Wang Xiangyu, He Xiaoyun, Wang Yunfei, Pan Zhangyuan, Chu Mingxing, Di Ran
Association Analyses between Single Nucleotide Polymorphisms in ZFAT, FBN1, FAM184B Genes and Litter Size of Xinggao Mutton Sheep
Gong Yiming et al. Association Analyses between Single Nucleotide Polymorphisms in ZFAT, FBN1, FAM184B Genes and Litter Size of Xinggao Mutton Sheep. . 2023-11-24. DOI: 10.3390/ani13233639 UGENTi001-A 2023-11-24 2023-11-24 DOI: 10.3390/ani13233639Associated cell lines:
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Zhuang Xinguo, Martin Tracey A., Ruge Fiona, Zeng Jianyuan (Jimmy), Li Xinyu (Amber), Khan Elyas, Dou Qingping, Davies Eleri, Jiang Wen G.
Expression of Claudin-9 (CLDN9) in Breast Cancer, the Clinical Significance in Connection with Its Subcoat Anchorage Proteins ZO-1 and ZO-3 and Impact on Drug Resistance
Zhuang Xinguo et al. Expression of Claudin-9 (CLDN9) in Breast Cancer, the Clinical Significance in Connection with Its Subcoat Anchorage Proteins ZO-1 and ZO-3 and Impact on Drug Resistance. . 2023-11-24. DOI: 10.3390/biomedicines11123136 BIONi010-C 2023-11-24 2023-11-24 DOI: 10.3390/biomedicines11123136Associated cell lines:
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Rocha Évilin, Bomfim Larissa, Junior Sérgio, Santos Gustavo, Meira Cássio, Soares Milena
Photodynamic Therapy with an Association of Methylene Blue and Toluidine Blue Promoted a Synergic Effect against Oral Squamous Cell Carcinoma
Rocha Évilin et al. Photodynamic Therapy with an Association of Methylene Blue and Toluidine Blue Promoted a Synergic Effect against Oral Squamous Cell Carcinoma. . 2023-11-22. DOI: 10.3390/cancers15235509 CBTCi001-A 2023-11-22 2023-11-22 DOI: 10.3390/cancers15235509Associated cell lines:
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Ragagnin Audrey M. G., Sundaramoorthy Vinod, Farzana Fabiha, Gautam Shashi, Saravanabavan Sayanthooran, Takalloo Zeinab, Mehta Prachi, Do-Ha Dzung, Parakh Sonam, Shadfar Sina, Hunter Julie, Vidal Marta, Jagaraj Cyril J., Brocardo Mariana, Konopka Anna, Yang Shu, Rayner Stephanie L., Williams Kelly L., Blair Ian P., Chung Roger S., Lee Albert, Ooi Lezanne, Atkin Julie D.
ALS/FTD-associated mutation in cyclin F inhibits ER-Golgi trafficking, inducing ER stress, ERAD and Golgi fragmentation
Ragagnin Audrey M. G. et al. ALS/FTD-associated mutation in cyclin F inhibits ER-Golgi trafficking, inducing ER stress, ERAD and Golgi fragmentation. . 2023-11-22. DOI: 10.1038/s41598-023-46802-9 UOWi005-A 2023-11-22 2023-11-22 DOI: 10.1038/s41598-023-46802-9Associated cell lines:
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Apaydin T, Zonis S, Zhou C, Valencia CW, Barrett R, Strous GJ, Mol JA, Chesnokova V, Melmed S
WIP1 is a novel specific target for growth hormone action
Apaydin T et al. WIP1 is a novel specific target for growth hormone action. . 2023-11-17. Pubmed ID: 37876819; DOI: 10.1016/j.isci.2023.108117; PMC: PMC10590974 EDi029-A 2023-11-17 2023-11-17 PubMed: 37876819 DOI: 10.1016/j.isci.2023.108117Associated cell lines:
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Martins‐Costa Catarina, Pham Vincent A, Sidhaye Jaydeep, Novatchkova Maria, Wiegers Andrea, Peer Angela, Möseneder Paul, Corsini Nina S, Knoblich Jürgen A
Morphogenesis and development of human telencephalic organoids in the absence and presence of exogenous extracellular matrix
Martins‐Costa Catarina et al. Morphogenesis and development of human telencephalic organoids in the absence and presence of exogenous extracellular matrix. . 2023-11-15. DOI: 10.15252/embj.2022113213 IMBAi001-A 2023-11-15 2023-11-15 DOI: 10.15252/embj.2022113213Associated cell lines:
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Loos M, Klampe B, Schulze T, Yin X, Theofilatos K, Ulmer BM, Schulz C, Behrens CS, van Bergen TD, Adami E, Maatz H, Schweizer M, Brodesser S, Skryabin BV, Rozhdestvensky TS, Bodbin S, Stathopoulou K, Christ T, Denning C, Hübner N, Mayr M, Cuello F, Eschenhagen T, Hansen A
Human model of primary carnitine deficiency cardiomyopathy reveals ferroptosis as a novel mechanism
Loos M et al. Human model of primary carnitine deficiency cardiomyopathy reveals ferroptosis as a novel mechanism. . 2023-11-14. Pubmed ID: 37802072; DOI: 10.1016/j.stemcr.2023.09.002; PMC: PMC10679537 UKEi001-A 2023-11-14 2023-11-14 PubMed: 37802072 DOI: 10.1016/j.stemcr.2023.09.002Associated cell lines:
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Schulz C, Sönmez M, Krause J, Schwedhelm E, Bangfen P, Alihodzic D, Hansen A, Eschenhagen T, Christ T
A critical role of retinoic acid concentration for the induction of a fully human-like atrial action potential phenotype in hiPSC-CM
Schulz C et al. A critical role of retinoic acid concentration for the induction of a fully human-like atrial action potential phenotype in hiPSC-CM. . 2023-11-14. Pubmed ID: 37922915; DOI: 10.1016/j.stemcr.2023.10.006; PMC: PMC10679650 UKEi001-AUKEi018-AUKEi021-A 2023-11-14 2023-11-14 PubMed: 37922915 DOI: 10.1016/j.stemcr.2023.10.006 -
Barbeau S, Semprez F, Dobbertin A, Merriadec L, Roussange F, Eymard B, Sternberg D, Fournier E, Karasoy H, Martinat C, Legay C
Molecular Analysis of a Congenital Myasthenic Syndrome Due to a Pathogenic Variant Affecting the C-Terminus of ColQ
Barbeau S et al. Molecular Analysis of a Congenital Myasthenic Syndrome Due to a Pathogenic Variant Affecting the C-Terminus of ColQ. . 2023-11-11. Pubmed ID: 38003406; DOI: 10.3390/ijms242216217; PMC: PMC10671321 REGUi009-A 2023-11-11 2023-11-11 PubMed: 38003406 DOI: 10.3390/ijms242216217Associated cell lines:
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Ramphan Suwipa, Chumchanchira Chanida, Sornjai Wannapa, Chailangkarn Thanathom, Jongkaewwattana Anan, Assavalapsakul Wanchai, Smith Duncan R.
Strain Variation Can Significantly Modulate the miRNA Response to Zika Virus Infection
Ramphan Suwipa et al. Strain Variation Can Significantly Modulate the miRNA Response to Zika Virus Infection. . 2023-11-11. DOI: 10.3390/ijms242216216 MUSIi011-AMUSIi011-B 2023-11-11 2023-11-11 DOI: 10.3390/ijms242216216Associated cell lines:
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Leal Andrés Felipe, Alméciga-Díaz Carlos Javier, Tomatsu Shunji
Mucopolysaccharidosis IVA: Current Disease Models and Drawbacks
Leal Andrés Felipe et al. Mucopolysaccharidosis IVA: Current Disease Models and Drawbacks. . 2023-11-09. DOI: 10.3390/ijms242216148 TRNDi005-A 2023-11-09 2023-11-09 DOI: 10.3390/ijms242216148Associated cell lines:
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Junge S, Ricci Signorini ME, Al Masri M, Gülink J, Brüning H, Kasperek L, Szepes M, Bakar M, Gruh I, Heisterkamp A, Torres-Mapa ML
A micro-LED array based platform for spatio-temporal optogenetic control of various cardiac models
Junge S et al. A micro-LED array based platform for spatio-temporal optogenetic control of various cardiac models. . 2023-11-09. Pubmed ID: 37945622; DOI: 10.1038/s41598-023-46149-1; PMC: PMC10636122 MHHi009-AMHHi009-A-3 2023-11-09 2023-11-09 PubMed: 37945622 DOI: 10.1038/s41598-023-46149-1Associated cell lines:
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Reyahi A, Studahl M, Skouboe MK, Fruhwürth S, Narita R, Ren F, Bjerhem Viklund M, Iversen MB, Christiansen M, Svensson A, Mogensen TH, Eriksson K, Paludan SR
An IKBKE variant conferring functional cGAS/STING pathway deficiency and susceptibility to recurrent HSV-2 meningitis
Reyahi A et al. An IKBKE variant conferring functional cGAS/STING pathway deficiency and susceptibility to recurrent HSV-2 meningitis. . 2023-11-08. Pubmed ID: 37937644; DOI: 10.1172/jci.insight.173066; PMC: PMC10721272 WTSIi015-A 2023-11-08 2023-11-08 PubMed: 37937644 DOI: 10.1172/jci.insight.173066Associated cell lines:
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Bocquet Béatrice, Borday Caroline, Erkilic Nejla, Mamaeva Daria, Donval Alicia, Masson Christel, Parain Karine, Kaminska Karolina, Quinodoz Mathieu, Perea-Romero Irene, Garcia-Garcia Gema, Jimenez-Medina Carla, Boukhaddaoui Hassan, Coget Arthur, Leboucq Nicolas, Calzetti Giacomo, Gandolfi Stefano, Percesepe Antonio, Barili Valeria, Uliana Vera, Delsante Marco, Bozzetti Francesca, Scholl Hendrik P.N., Corton Marta, Ayuso Carmen, Millan Jose M., Rivolta Carlo, Meunier Isabelle, Perron Muriel, Kalatzis Vasiliki
TBC1D32 variants disrupt retinal ciliogenesis and cause retinitis pigmentosa
Bocquet Béatrice et al. TBC1D32 variants disrupt retinal ciliogenesis and cause retinitis pigmentosa. . 2023-11-08. DOI: 10.1172/jci.insight.169426 INMi004-A 2023-11-08 2023-11-08 DOI: 10.1172/jci.insight.169426Associated cell lines:
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Liu Yanjiang, Hu Gongcheng, Yang Shengxiong, Yao Mingze, Liu Zicong, Yan Chenghong, Wen Yulin, Ping Wangfang, Wang Juehan, Song Yawei, Dong Xiaotao, Pan Guangjin, Yao Hongjie
Functional dissection of PRC1 subunits RYBP and YAF2 during neural differentiation of embryonic stem cells
Liu Yanjiang et al. Functional dissection of PRC1 subunits RYBP and YAF2 during neural differentiation of embryonic stem cells. . 2023-11-07. DOI: 10.1038/s41467-023-42507-9 GIBHe001-A 2023-11-07 2023-11-07 DOI: 10.1038/s41467-023-42507-9Associated cell lines:
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De Sousa Paul A, Perfect Leo, Ye Jinpei, Samuels Kay, Piotrowska Ewa, Gordon Martin, Abranches Elsa, Wishart Thomas M, Dockrell David H, Courtney Aidan, Mate Ryan
Hyaluronan in mesenchymal stromal cell lineage differentiation from human pluripotent stem cells: Application in serum free culture
De Sousa Paul A et al. Hyaluronan in mesenchymal stromal cell lineage differentiation from human pluripotent stem cells: Application in serum free culture. . 2023-11-07. DOI: 10.21203/rs.3.rs-3433788/v1 RCe013-A 2023-11-07 2023-11-07 DOI: 10.21203/rs.3.rs-3433788/v1Associated cell lines:
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Blümke A, Ijeoma E, Simon J, Wellington R, Purwaningrum M, Doulatov S, Leber E, Scatena M, Giachelli CM
Comparison of osteoclast differentiation protocols from human induced pluripotent stem cells of different tissue origins
Blümke A et al. Comparison of osteoclast differentiation protocols from human induced pluripotent stem cells of different tissue origins. . 2023-11-07. Pubmed ID: 37936199; DOI: 10.1186/s13287-023-03547-6; PMC: PMC10631132 RTIBDi001-ACIMRi001-A 2023-11-07 2023-11-07 PubMed: 37936199 DOI: 10.1186/s13287-023-03547-6Associated cell lines:
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Holst Mikkel Roland, de Wit Nienke Marije, Ozgür Burak, Brachner Andreas, Hyldig Kathrine, Appelt-Menzel Antje, Sleven Hannah, Cader Zameel, de Vries Helga Eveline, Neuhaus Winfried, Jensen Allan, Brodin Birger, Nielsen Morten Schallburg
Subcellular trafficking and transcytosis efficacy of different receptor types for therapeutic antibody delivery at the blood‒brain barrier
Holst Mikkel Roland et al. Subcellular trafficking and transcytosis efficacy of different receptor types for therapeutic antibody delivery at the blood‒brain barrier. . 2023-11-06. DOI: 10.1186/s12987-023-00480-x BIONi010-C 2023-11-06 2023-11-06 DOI: 10.1186/s12987-023-00480-xAssociated cell lines:
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Mueller Laura M., Isaacson Abigail, Wilson Heather, Salowka Anna, Gong Maolian, Raile Klemens, Spagnoli Francesca M.
Heterozygous missense variant inGLI2impairs human endocrine pancreas development
Mueller Laura M. et al. Heterozygous missense variant inGLI2impairs human endocrine pancreas development. . 2023-11-05. DOI: 10.1101/2023.11.05.565673 HMGUi001-A 2023-11-05 2023-11-05 DOI: 10.1101/2023.11.05.565673Associated cell lines:
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Zhou L, Li H, Sun T, Wen X, Niu C, Li M, Li W, Esteban MA, Hoffman AR, Hu JF, Cui J
Profiling mitochondria-polyribosome lncRNAs associated with pluripotency
Zhou L et al. Profiling mitochondria-polyribosome lncRNAs associated with pluripotency. . 2023-11-02. Pubmed ID: 37919270; DOI: 10.1038/s41597-023-02649-3; PMC: PMC10622415 WAe009-A 2023-11-02 2023-11-02 PubMed: 37919270 DOI: 10.1038/s41597-023-02649-3Associated cell lines:
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Rogala S, Ali T, Melissari MT, Währisch S, Schuster P, Sarre A, Emídio RC, Boettger T, Rogg EM, Kaur J, Krishnan J, Dumbović G, Dimmeler S, Ounzain S, Pedrazzini T, Herrmann BG, Grote P
The lncRNA Sweetheart regulates compensatory cardiac hypertrophy after myocardial injury in murine males
Rogala S et al. The lncRNA Sweetheart regulates compensatory cardiac hypertrophy after myocardial injury in murine males. . 2023-11-02. Pubmed ID: 37919291; DOI: 10.1038/s41467-023-42760-y; PMC: PMC10622434 WTSIi081-A 2023-11-02 2023-11-02 PubMed: 37919291 DOI: 10.1038/s41467-023-42760-yAssociated cell lines:
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Tyagi Nishu, Uppili Bharathram, Sharma Pooja, Parveen Shaista, Saifi Sheeba, Jain Abhinav, Sonakar Akhilesh, Ahmed Istaq, Sahni Shweta, Shamim Uzma, Anand Avni, Suroliya Varun, Asokachandran Vivekanand, Srivastava Achal, Sivasubbu Sridhar, Scaria Vinod, Faruq Mohammed
Investigation of RFC1 tandem nucleotide repeat locus in diverse neurodegenerative outcomes in an Indian cohort
Tyagi Nishu et al. Investigation of RFC1 tandem nucleotide repeat locus in diverse neurodegenerative outcomes in an Indian cohort. . 2023-11-02. DOI: 10.1007/s10048-023-00736-6 IGIBi002-AIGIBi003-AIGIBi004-A 2023-11-02 2023-11-02 DOI: 10.1007/s10048-023-00736-6Associated cell lines:
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Múnera JO, Kechele DO, Bouffi C, Qu N, Jing R, Maity P, Enriquez JR, Han L, Campbell I, Mahe MM, McCauley HA, Zhang X, Sundaram N, Hudson JR, Zarsozo-Lacoste A, Pradhan S, Tominaga K, Sanchez JG, Weiss AA, Chatuvedi P, Spence JR, Hachimi M, North T, Daley GQ, Mayhew CN, Hu YC, Takebe T, Helmrath MA, Wells JM
Development of functional resident macrophages in human pluripotent stem cell-derived colonic organoids and human fetal colon
Múnera JO et al. Development of functional resident macrophages in human pluripotent stem cell-derived colonic organoids and human fetal colon. . 2023-11-02. Pubmed ID: 37922878; DOI: 10.1016/j.stem.2023.10.002; PMC: PMC10913028 CUSTOMi001-A 2023-11-02 2023-11-02 PubMed: 37922878 DOI: 10.1016/j.stem.2023.10.002Associated cell lines:
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Sarieva K, Hildebrand F, Kagermeier T, Yentür Z, Becker K, Mayer S
Pluripotent stem cell-derived neural progenitor cells can be used to model effects of IL-6 on human neurodevelopment
Sarieva K et al. Pluripotent stem cell-derived neural progenitor cells can be used to model effects of IL-6 on human neurodevelopment. . 2023-11-01. Pubmed ID: 37921007; DOI: 10.1242/dmm.050306; PMC: PMC10629675 BIONi010-C 2023-11-01 2023-11-01 PubMed: 37921007 DOI: 10.1242/dmm.050306Associated cell lines:
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Dirck A, Diggins NL, Crawford LB, Perez WD, Parkins CJ, Struthers HH, Turner R, Pham AH, Mitchell J, Papen CR, Malouli D, Hancock MH, Caposio P
HCMV UL8 interaction with β-catenin and DVL2 regulates viral reactivation in CD34(+) hematopoietic progenitor cells
Dirck A et al. HCMV UL8 interaction with β-catenin and DVL2 regulates viral reactivation in CD34(+) hematopoietic progenitor cells. . 2023-10-31. Pubmed ID: 37772824; DOI: 10.1128/jvi.01241-23; PMC: PMC10617580 WAe001-A 2023-10-31 2023-10-31 PubMed: 37772824 DOI: 10.1128/jvi.01241-23Associated cell lines:
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Rani S, Thamodaran V, Nandy K, Fouzia NA, Maddali M, Rajesh P, Vijayanand S, David E, Velayudhan SR
Establishment and characterization of CSCRi006-A: an induced pluripotent stem cell line generated from a patient with Diamond-Blackfan Anemia (DBA) carrying ribosomal protein S19 (RPS19) mutation
Rani S et al. Establishment and characterization of CSCRi006-A: an induced pluripotent stem cell line generated from a patient with Diamond-Blackfan Anemia (DBA) carrying ribosomal protein S19 (RPS19) mutation. . 2023-11-00. Pubmed ID: 37603219; DOI: 10.1007/s13577-023-00946-y CSCRi006-A 2023-11-00 2023-11-00 PubMed: 37603219 DOI: 10.1007/s13577-023-00946-yAssociated cell lines:
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Ori Chaido, Ansari Meshal, Angelidis Ilias, Olmer Ruth, Martin Ulrich, Theis Fabian J., Schiller Herbert B., Drukker Micha
Human pluripotent stem cell fate trajectories toward lung and hepatocyte progenitors
Ori Chaido et al. Human pluripotent stem cell fate trajectories toward lung and hepatocyte progenitors. . 2023-11-00. DOI: 10.1016/j.isci.2023.108205 MHHi006-AMHHi006-A-2 2023-11-00 2023-11-00 DOI: 10.1016/j.isci.2023.108205Associated cell lines:
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Lin Chaohui, Kuffour Edmund Osei, Fuchs Nina V., Gertzen Christoph G.W., Kaiser Jesko, Hirschenberger Maximilian, Tang Xiao, Xu Haifeng C., Michel Oliver, Tao Ronny, Haase Alexandra, Martin Ulrich, Kurz Thomas, Drexler Ingo, Görg Boris, Lang Philipp A., Luedde Tom, Sparrer Konstantin M.J., Gohlke Holger, König Renate, Münk Carsten
Regulation of STING activity in DNA sensing by ISG15 modification
Lin Chaohui et al. Regulation of STING activity in DNA sensing by ISG15 modification. . 2023-11-00. DOI: 10.1016/j.celrep.2023.113277 PEIi003-A 2023-11-00 2023-11-00 DOI: 10.1016/j.celrep.2023.113277Associated cell lines:
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Lotfi Malihe, Morshedi Rad Dorsa, Mashhadi Samaneh Sharif, Ashouri Atefeh, Mojarrad Majid, Mozaffari-Jovin Sina, Farrokhi Shima, Hashemi Maryam, Lotfi Marzieh, Ebrahimi Warkiani Majid, Abbaszadegan Mohammad Reza
Recent Advances in CRISPR/Cas9 Delivery Approaches for Therapeutic Gene Editing of Stem Cells
Lotfi Malihe et al. Recent Advances in CRISPR/Cas9 Delivery Approaches for Therapeutic Gene Editing of Stem Cells. . 2023-11-00. DOI: 10.1007/s12015-023-10585-3 MCRIi001-AMCRIi001-A-1 2023-11-00 2023-11-00 DOI: 10.1007/s12015-023-10585-3Associated cell lines:
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Jacobs Johanna, Van Aelst Lucas, Breckpot Jeroen, Corveleyn Anniek, Kuiperi Cuno, Dupont Matthias, Heggermont Ward, De Vadder Katrien, Willems Rik, Van Cleemput Johan, Bogaert Jan G., Robyns Tomas
Tools to differentiate between Filamin C and Titin truncating variant carriers: value of MRI
Jacobs Johanna et al. Tools to differentiate between Filamin C and Titin truncating variant carriers: value of MRI. . 2023-11-00. DOI: 10.1038/s41431-023-01357-1 YCMi004-A 2023-11-00 2023-11-00 DOI: 10.1038/s41431-023-01357-1Associated cell lines:
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Haferkamp U, Hartmann C, Abid CL, Brachner A, Höchner A, Gerhartl A, Harwardt B, Leckzik S, Leu J, Metzger M, Nastainczyk-Wulf M, Neuhaus W, Oerter S, Pless O, Rujescu D, Jung M, Appelt-Menzel A
Human isogenic cells of the neurovascular unit exert transcriptomic cell type-specific effects on a blood-brain barrier in vitro model of late-onset Alzheimer disease
Haferkamp U et al. Human isogenic cells of the neurovascular unit exert transcriptomic cell type-specific effects on a blood-brain barrier in vitro model of late-onset Alzheimer disease. . 2023-10-31. Pubmed ID: 37907966; DOI: 10.1186/s12987-023-00471-y; PMC: PMC10617216 WISCi004-BZIPi013-BMLUi008-AMLUi009-AMLUi007-JMLUi010-B 2023-10-31 2023-10-31 PubMed: 37907966 DOI: 10.1186/s12987-023-00471-y -
Windt L.M., Wiendels M., Dostanić M., Bellin M., Sarro P.M., Mastrangeli M., Mummery C.L., van Meer B.J.
Miniaturized engineered heart tissues from hiPSC-derived triple cell type co-cultures to study human cardiac function
Windt L.M. et al. Miniaturized engineered heart tissues from hiPSC-derived triple cell type co-cultures to study human cardiac function. . 2023-11-00. DOI: 10.1016/j.bbrc.2023.09.034 LUMCi028-A 2023-11-00 2023-11-00 DOI: 10.1016/j.bbrc.2023.09.034Associated cell lines:
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De Pablo-Moreno Juan A., Miguel-Batuecas Andrea, Rodríguez-Merchán E. Carlos, Liras Antonio
Treatment of congenital coagulopathies, from biologic to biotechnological drugs: The relevance of gene editing (CRISPR/Cas)
De Pablo-Moreno Juan A. et al. Treatment of congenital coagulopathies, from biologic to biotechnological drugs: The relevance of gene editing (CRISPR/Cas). . 2023-11-00. DOI: 10.1016/j.thromres.2023.10.001 YCMi001-BYCMi001-B-1 2023-11-00 2023-11-00 DOI: 10.1016/j.thromres.2023.10.001Associated cell lines:
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Xu Lei, Zeng Quan, Liang Liqing, Yang Zhou, Qu Mingyi, Li Huilin, Zhang Bowen, Zhang Jing, Yuan Xin, Chen Lin, Fan Zeng, He Lijuan, Nan Xue, Yue Wen, Xie Xiaoyan, Pei Xuetao
Generation of Rh D‐negative blood using
Xu Lei et al. Generation of Rh D‐negative blood usingCRISPR /Cas9 CRISPR /Cas9 . . 2023-11-00. DOI: 10.1111/cpr.13486 IHSTMi001-AKRIBBi001-A 2023-11-00 2023-11-00 DOI: 10.1111/cpr.13486Associated cell lines:
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Burgio F, Gaiser C, Brady K, Gatta V, Class R, Schrage R, Suter-Dick L
A Perfused In Vitro Human iPSC-Derived Blood-Brain Barrier Faithfully Mimics Transferrin Receptor-Mediated Transcytosis of Therapeutic Antibodies
Burgio F et al. A Perfused In Vitro Human iPSC-Derived Blood-Brain Barrier Faithfully Mimics Transferrin Receptor-Mediated Transcytosis of Therapeutic Antibodies. . 2023-11-00. Pubmed ID: 37698826; DOI: 10.1007/s10571-023-01404-x; PMC: PMC10661771 SIGi001-ASIGi001-A-2 2023-11-00 2023-11-00 PubMed: 37698826 DOI: 10.1007/s10571-023-01404-xAssociated cell lines:
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Zhang Li, Yu Li, Shu Xianhong, Ding Jing, Zhou Jingmin, Zhong Chunjiu, Pan Baishen, Guo Wei, Zhang Chunyan, Wang Beili
Whole exome sequencing reveal 83 novel Mendelian disorders carrier P/LP variants in Chinese adult patients
Zhang Li et al. Whole exome sequencing reveal 83 novel Mendelian disorders carrier P/LP variants in Chinese adult patients. . 2023-11-00. DOI: 10.1038/s10038-023-01179-5 SDQLCHi035-A 2023-11-00 2023-11-00 DOI: 10.1038/s10038-023-01179-5Associated cell lines:
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Cukier HN, Duarte CL, Laverde-Paz MJ, Simon SA, Van Booven DJ, Miyares AT, Whitehead PL, Hamilton-Nelson KL, Adams LD, Carney RM, Cuccaro ML, Vance JM, Pericak-Vance MA, Griswold AJ, Dykxhoorn DM
An Alzheimer's disease risk variant in TTC3 modifies the actin cytoskeleton organization and the PI3K-Akt signaling pathway in iPSC-derived forebrain neurons
Cukier HN et al. An Alzheimer's disease risk variant in TTC3 modifies the actin cytoskeleton organization and the PI3K-Akt signaling pathway in iPSC-derived forebrain neurons. . 2023-11-00. Pubmed ID: 37677864; DOI: 10.1016/j.neurobiolaging.2023.07.007; PMC: PMC10538380 UMi028-AUMi028-A-2 2023-11-00 2023-11-00 PubMed: 37677864 DOI: 10.1016/j.neurobiolaging.2023.07.007Associated cell lines:
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He Rong, Weng Zhijie, Liu Yunkun, Li Bingzhi, Wang Wenxuan, Meng Wanrong, Li Bo, Li Longjiang
Application of Induced Pluripotent Stem Cells in Malignant Solid Tumors
He Rong et al. Application of Induced Pluripotent Stem Cells in Malignant Solid Tumors. . 2023-11-00. DOI: 10.1007/s12015-023-10633-y KMUGMCi004-A 2023-11-00 2023-11-00 DOI: 10.1007/s12015-023-10633-yAssociated cell lines:
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Fan X, Yang G, Duru F, Grilli M, Akin I, Zhou X, Saguner AM, Ei-Battrawy I
Arrhythmogenic Cardiomyopathy: from Preclinical Models to Genotype-phenotype Correlation and Pathophysiology
Fan X et al. Arrhythmogenic Cardiomyopathy: from Preclinical Models to Genotype-phenotype Correlation and Pathophysiology. . 2023-11-00. Pubmed ID: 37731079; DOI: 10.1007/s12015-023-10615-0; PMC: PMC10661732 HUBUi001-AUSFi004-A 2023-11-00 2023-11-00 PubMed: 37731079 DOI: 10.1007/s12015-023-10615-0Associated cell lines:
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Li H, Zhang Q, Wan R, Zhou L, Xu X, Xu C, Yu Y, Xu Y, Xiang Y, Tang S
PLPPR4 haploinsufficiency causes neurodevelopmental disorders by disrupting synaptic plasticity via mTOR signalling
Li H et al. PLPPR4 haploinsufficiency causes neurodevelopmental disorders by disrupting synaptic plasticity via mTOR signalling. . 2023-11-00. Pubmed ID: 37550884; DOI: 10.1111/jcmm.17899; PMC: PMC10623522 CHWi001-A 2023-11-00 2023-11-00 PubMed: 37550884 DOI: 10.1111/jcmm.17899Associated cell lines:
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Amore Greta, Calì Elisa, Spanò Maria, Ceravolo Giorgia, Mangano Giuseppe Donato, Scorrano Giovanna, Efthymiou Stephanie, Salpietro Vincenzo, Houlden Henry, Di Rosa Gabriella
ATP6V1B2-related disorders featuring Lennox-Gastaut-syndrome: A case-based overview
Amore Greta et al. ATP6V1B2-related disorders featuring Lennox-Gastaut-syndrome: A case-based overview. . 2023-11-00. DOI: 10.1016/j.braindev.2023.07.004 CPGHi002-A 2023-11-00 2023-11-00 DOI: 10.1016/j.braindev.2023.07.004Associated cell lines:
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Ge N, Liu M, Li R, Allen NM, Galvin J, Shen S, O'Brien T, Prendiville TW
Using Ribonucleoprotein-based CRISPR/Cas9 to Edit Single Nucleotide on Human Induced Pluripotent Stem Cells to Model Type 3 Long QT Syndrome (SCN5A(±))
Ge N et al. Using Ribonucleoprotein-based CRISPR/Cas9 to Edit Single Nucleotide on Human Induced Pluripotent Stem Cells to Model Type 3 Long QT Syndrome (SCN5A(±)). . 2023-11-00. Pubmed ID: 37653182; DOI: 10.1007/s12015-023-10602-5; PMC: PMC10661835 NUIGi018-ANUIGi038-ANUIGi038-B 2023-11-00 2023-11-00 PubMed: 37653182 DOI: 10.1007/s12015-023-10602-5Associated cell lines:
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Li Liwei, Huang Chunman, Pang Jingqun, Huang Yongbin, Chen Xinxin, Chen Guanghua
Advances in research on cell models for skeletal muscle atrophy
Li Liwei et al. Advances in research on cell models for skeletal muscle atrophy. . 2023-11-00. DOI: 10.1016/j.biopha.2023.115517 ORIONi003-A 2023-11-00 2023-11-00 DOI: 10.1016/j.biopha.2023.115517Associated cell lines:
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Diaw SH, Borsche M, Streubel-Gallasch L, Dulovic-Mahlow M, Hermes J, Lenz I, Seibler P, Klein C, Brüggemann N, Vos M, Lohmann K
Characterization of the pathogenic α-Synuclein Variant V15A in Parkinson´s disease
Diaw SH et al. Characterization of the pathogenic α-Synuclein Variant V15A in Parkinson´s disease. . 2023-10-30. Pubmed ID: 37903765; DOI: 10.1038/s41531-023-00584-z; PMC: PMC10616187 STBCi033-BSTBCi052-CSTBCi053-ASTBCi101-A 2023-10-30 2023-10-30 PubMed: 37903765 DOI: 10.1038/s41531-023-00584-zAssociated cell lines:
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Shoda Hirofumi, Natsumoto Bunki, Fujio Keishi
Investigation of immune-related diseases using patient-derived induced pluripotent stem cells
Shoda Hirofumi et al. Investigation of immune-related diseases using patient-derived induced pluripotent stem cells. . 2023-10-24. DOI: 10.1186/s41232-023-00303-4 XDCMHi001-ASHFDi001-AIMAGINi011-ASPHi001-ADMBi003-ADMBi004-A 2023-10-24 2023-10-24 DOI: 10.1186/s41232-023-00303-4Associated cell lines:
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Stüdle C, Nishihara H, Wischnewski S, Kulsvehagen L, Perriot S, Ishikawa H, Schroten H, Frank S, Deigendesch N, Du Pasquier R, Schirmer L, Pröbstel AK, Engelhardt B
SARS-CoV-2 infects epithelial cells of the blood-cerebrospinal fluid barrier rather than endothelial cells or pericytes of the blood-brain barrier
Stüdle C et al. SARS-CoV-2 infects epithelial cells of the blood-cerebrospinal fluid barrier rather than endothelial cells or pericytes of the blood-brain barrier. . 2023-10-24. Pubmed ID: 37875964; DOI: 10.1186/s12987-023-00479-4; PMC: PMC10598911 LNISi001-ALNISi001-BLNISi002-ALNISi002-BLNISi003-ALNISi003-BLNISi004-ALNISi004-B 2023-10-24 2023-10-24 PubMed: 37875964 DOI: 10.1186/s12987-023-00479-4Associated cell lines:
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van Loo B, Ten Den SA, Araújo-Gomes N, de Jong V, Snabel RR, Schot M, Rivera-Arbeláez JM, Veenstra GJC, Passier R, Kamperman T, Leijten J
Mass production of lumenogenic human embryoid bodies and functional cardiospheres using in-air-generated microcapsules
van Loo B et al. Mass production of lumenogenic human embryoid bodies and functional cardiospheres using in-air-generated microcapsules. . 2023-10-21. Pubmed ID: 37865642; DOI: 10.1038/s41467-023-42297-0; PMC: PMC10590445 ESIBIe003-A 2023-10-21 2023-10-21 PubMed: 37865642 DOI: 10.1038/s41467-023-42297-0Associated cell lines:
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Harper TC, Oberlick EM, Smith TJ, Nunes DE, Bray MA, Park S, Driscoll CD, Mowbray SF, Antczak C
GATA1 deletion in human pluripotent stem cells increases differentiation yield and maturity of neutrophils
Harper TC et al. GATA1 deletion in human pluripotent stem cells increases differentiation yield and maturity of neutrophils. . 2023-10-20. Pubmed ID: 37720099; DOI: 10.1016/j.isci.2023.107804; PMC: PMC10500457 WAe001-A 2023-10-20 2023-10-20 PubMed: 37720099 DOI: 10.1016/j.isci.2023.107804Associated cell lines:
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Camões dos Santos João, Appleton Carolina, Cazaux Mateus Francisca, Covas Rita, Bekman Evguenia Pavlovna, da Rocha Simão Teixeira
Stem cell models of Angelman syndrome
Camões dos Santos João et al. Stem cell models of Angelman syndrome. . 2023-10-19. DOI: 10.3389/fcell.2023.1274040 IBBISTi004-A 2023-10-19 2023-10-19 DOI: 10.3389/fcell.2023.1274040Associated cell lines:
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Katolikova NV, Vaganova AN, Shafranskaya DD, Efimova EV, Malashicheva AB, Gainetdinov RR
Expression Pattern of Trace Amine-Associated Receptors during Differentiation of Human Pluripotent Stem Cells to Dopaminergic Neurons
Katolikova NV et al. Expression Pattern of Trace Amine-Associated Receptors during Differentiation of Human Pluripotent Stem Cells to Dopaminergic Neurons. . 2023-10-18. Pubmed ID: 37894992; DOI: 10.3390/ijms242015313; PMC: PMC10607858 WTSIi004-AWTSIi032-AWTSIi046-A 2023-10-18 2023-10-18 PubMed: 37894992 DOI: 10.3390/ijms242015313Associated cell lines:
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Kayser A, Dittmann S, Šarić T, Mearini G, Verkerk AO, Schulze-Bahr E
The W101C KCNJ5 Mutation Induces Slower Pacing by Constitutively Active GIRK Channels in hiPSC-Derived Cardiomyocytes
Kayser A et al. The W101C KCNJ5 Mutation Induces Slower Pacing by Constitutively Active GIRK Channels in hiPSC-Derived Cardiomyocytes. . 2023-10-18. Pubmed ID: 37894977; DOI: 10.3390/ijms242015290; PMC: PMC10607318 UKMi005-AUKMi006-A 2023-10-18 2023-10-18 PubMed: 37894977 DOI: 10.3390/ijms242015290 -
Jaratsittisin Janejira, Sornjai Wannapa, Chailangkarn Thanathom, Jongkaewwattana Anan, Smith Duncan R.
The vitamin D receptor agonist EB1089 can exert its antiviral activity independently of the vitamin D receptor
Jaratsittisin Janejira et al. The vitamin D receptor agonist EB1089 can exert its antiviral activity independently of the vitamin D receptor. . 2023-10-17. DOI: 10.1371/journal.pone.0293010 MUSIi011-AMUSIi011-B 2023-10-17 2023-10-17 DOI: 10.1371/journal.pone.0293010Associated cell lines:
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Cheng R, Zhou S, K C R, Lizarazo S, Mouli L, Jayanth A, Liu Q, Van Bortle K
A Combinatorial Regulatory Platform Determines Expression of RNA Polymerase III Subunit RPC7α (POLR3G) in Cancer
Cheng R et al. A Combinatorial Regulatory Platform Determines Expression of RNA Polymerase III Subunit RPC7α (POLR3G) in Cancer. . 2023-10-15. Pubmed ID: 37894362; DOI: 10.3390/cancers15204995; PMC: PMC10605170 WAe001-A 2023-10-15 2023-10-15 PubMed: 37894362 DOI: 10.3390/cancers15204995Associated cell lines:
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Aitova A, Berezhnoy A, Tsvelaya V, Gusev O, Lyundup A, Efimov AE, Agapov I, Agladze K
Biomimetic Cardiac Tissue Models for In Vitro Arrhythmia Studies
Aitova A et al. Biomimetic Cardiac Tissue Models for In Vitro Arrhythmia Studies. . 2023-10-14. Pubmed ID: 37887618; DOI: 10.3390/biomimetics8060487; PMC: PMC10604593 LUMCi028-ALUMCi039-A 2023-10-14 2023-10-14 PubMed: 37887618 DOI: 10.3390/biomimetics8060487Associated cell lines:
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Oliveira Julia Teixeira, Yanick Christopher, Wein Nicolas, Gomez Limia Cintia Elisabeth
Neuron-Schwann cell interactions in peripheral nervous system homeostasis, disease, and preclinical treatment
Oliveira Julia Teixeira et al. Neuron-Schwann cell interactions in peripheral nervous system homeostasis, disease, and preclinical treatment. . 2023-10-12. DOI: 10.3389/fncel.2023.1248922 JUCTCi019-A 2023-10-12 2023-10-12 DOI: 10.3389/fncel.2023.1248922Associated cell lines:
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Lamiable A, Champetier T, Leonardi F, Cohen E, Sommer P, Hardy D, Argy N, Massougbodji A, Del Nery E, Cottrell G, Kwon YJ, Genovesio A
Revealing invisible cell phenotypes with conditional generative modeling
Lamiable A et al. Revealing invisible cell phenotypes with conditional generative modeling. . 2023-10-11. Pubmed ID: 37821450; DOI: 10.1038/s41467-023-42124-6; PMC: PMC10567685 STBCi004-B 2023-10-11 2023-10-11 PubMed: 37821450 DOI: 10.1038/s41467-023-42124-6Associated cell lines:
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Bressan C, Snapyan M, Snapyan M, Klaus J, di Matteo F, Robertson SP, Treutlein B, Parent M, Cappello S, Saghatelyan A
Metformin rescues migratory deficits of cells derived from patients with periventricular heterotopia
Bressan C et al. Metformin rescues migratory deficits of cells derived from patients with periventricular heterotopia. . 2023-10-11. Pubmed ID: 37609821; DOI: 10.15252/emmm.202216908; PMC: PMC10565636 ISFi001-A 2023-10-11 2023-10-11 PubMed: 37609821 DOI: 10.15252/emmm.202216908Associated cell lines:
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Sprenkeler Evelien G. G., Goetschalckx Ines, Fernández Hermira Sara, Tool Anton T. J., Hoogenboezem Mark, van Bruggen Robin, Kuijpers Taco W.
Lack of eosinophil extracellular trap formation due to failure of plasma membrane breakdown in the absence of elastase
Sprenkeler Evelien G. G. et al. Lack of eosinophil extracellular trap formation due to failure of plasma membrane breakdown in the absence of elastase. . 2023-10-10. DOI: 10.1182/bloodadvances.2022009432 SANi007-A 2023-10-10 2023-10-10 DOI: 10.1182/bloodadvances.2022009432Associated cell lines:
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van der Wal E, Iuliano A, In 't Groen SLM, Bholasing AP, Priesmann D, Sharma P, den Hamer B, Saggiomo V, Krüger M, Pijnappel WWMP, de Greef JC
Highly contractile 3D tissue engineered skeletal muscles from human iPSCs reveal similarities with primary myoblast-derived tissues
van der Wal E et al. Highly contractile 3D tissue engineered skeletal muscles from human iPSCs reveal similarities with primary myoblast-derived tissues. . 2023-10-10. Pubmed ID: 37774701; DOI: 10.1016/j.stemcr.2023.08.014; PMC: PMC10656354 LUMCi002-ALUMCi003-ALUMCi023-A 2023-10-10 2023-10-10 PubMed: 37774701 DOI: 10.1016/j.stemcr.2023.08.014Associated cell lines:
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Rosowski S, Remmert C, Marder M, Akishiba M, Bushe J, Feuchtinger A, Platen A, Ussar S, Theis F, Wiedenmann S, Meier M
Single-cell characterization of neovascularization using hiPSC-derived endothelial cells in a 3D microenvironment
Rosowski S et al. Single-cell characterization of neovascularization using hiPSC-derived endothelial cells in a 3D microenvironment. . 2023-10-10. Pubmed ID: 37714147; DOI: 10.1016/j.stemcr.2023.08.008; PMC: PMC10656300 HMGUi002-A 2023-10-10 2023-10-10 PubMed: 37714147 DOI: 10.1016/j.stemcr.2023.08.008Associated cell lines:
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Tao J.Q.
Coffin-Siris syndrome caused by a de novo mutation in ARID1B: a case report and literature review
Tao J.Q.. Coffin-Siris syndrome caused by a de novo mutation in ARID1B: a case report and literature review. . 2023-10-10. DOI: 10.11852/zgetbjzz2022-1405 SDQLCHi045-A 2023-10-10 2023-10-10 DOI: 10.11852/zgetbjzz2022-1405Associated cell lines:
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Srivastava Apeksha, Chauhan Shikha, Ahuja Vishal
Recent advances in CRISPR/Cas9-assisted gene therapy
Srivastava Apeksha et al. Recent advances in CRISPR/Cas9-assisted gene therapy. . 2023-10-10. DOI: 10.33640/2405-609x.3330 MCRIi001-AMCRIi001-A-1 2023-10-10 2023-10-10 DOI: 10.33640/2405-609x.3330Associated cell lines:
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Liu T, Dai X, Xu Y, Guan T, Hong L, Zaib T, Zhou Q, Cheng K, Zhou X, Ma C, Sun P
CD22 is a potential target of CAR-NK cell therapy for esophageal squamous cell carcinoma
Liu T et al. CD22 is a potential target of CAR-NK cell therapy for esophageal squamous cell carcinoma. . 2023-10-10. Pubmed ID: 37817249; DOI: 10.1186/s12967-023-04409-8; PMC: PMC10563326 UKKi011-A 2023-10-10 2023-10-10 PubMed: 37817249 DOI: 10.1186/s12967-023-04409-8Associated cell lines:
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Fiock KL, Hook JN, Hefti MM
Determinants of astrocytic pathology in stem cell models of primary tauopathies
Fiock KL et al. Determinants of astrocytic pathology in stem cell models of primary tauopathies. . 2023-10-06. Pubmed ID: 37803326; DOI: 10.1186/s40478-023-01655-1; PMC: PMC10557325 WAe014-A 2023-10-06 2023-10-06 PubMed: 37803326 DOI: 10.1186/s40478-023-01655-1Associated cell lines:
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Ren F, Narita R, Rashidi AS, Fruhwürth S, Gao Z, Bak RO, Thomsen MK, Verjans GM, Reinert LS, Paludan SR
ER stress induces caspase-2-tBID-GSDME-dependent cell death in neurons lytically infected with herpes simplex virus type 2
Ren F et al. ER stress induces caspase-2-tBID-GSDME-dependent cell death in neurons lytically infected with herpes simplex virus type 2. . 2023-10-04. Pubmed ID: 37646198; DOI: 10.15252/embj.2022113118; PMC: PMC10548179 WTSIi015-A 2023-10-04 2023-10-04 PubMed: 37646198 DOI: 10.15252/embj.2022113118Associated cell lines:
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ERGİN Ahmet Doğan, SEÇEN Erhan, UNER Burcu, ÇELİK Aybuke
Coenzyme Q10 Loaded DQAsomes for Leigh Disease
ERGİN Ahmet Doğan et al. Coenzyme Q10 Loaded DQAsomes for Leigh Disease. . 2023-10-03. DOI: 10.21203/rs.3.rs-3370616/v1 MDCi007-A 2023-10-03 2023-10-03 DOI: 10.21203/rs.3.rs-3370616/v1Associated cell lines:
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Lim CM, González Díaz A, Fuxreiter M, Pun FW, Zhavoronkov A, Vendruscolo M
Multiomic prediction of therapeutic targets for human diseases associated with protein phase separation
Lim CM et al. Multiomic prediction of therapeutic targets for human diseases associated with protein phase separation. . 2023-10-03. Pubmed ID: 37774095; DOI: 10.1073/pnas.2300215120; PMC: PMC10556643 BIONi010-CBIONi010-C-38 2023-10-03 2023-10-03 PubMed: 37774095 DOI: 10.1073/pnas.2300215120Associated cell lines:
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Sanal Madhusudana Girija, Gupta Sarita, Saha Rahul, Vats Nisha, Sarin Shiv Kumar
Hepatitis B Virus x Protein Increases Cellular OCT3/4 and MYC and Facilitates Cellular Reprogramming
Sanal Madhusudana Girija et al. Hepatitis B Virus x Protein Increases Cellular OCT3/4 and MYC and Facilitates Cellular Reprogramming. . 2023-10-01. DOI: 10.1089/cell.2023.0055 NCCSi008-ANCCSi008-B 2023-10-01 2023-10-01 DOI: 10.1089/cell.2023.0055Associated cell lines:
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Rossiaud L, Pellier E, Benabides M, Nissan X, Ronzitti G, Hoch L
Generation of three induced pluripotent stem cell lines from patients with glycogen storage disease type III
Rossiaud L et al. Generation of three induced pluripotent stem cell lines from patients with glycogen storage disease type III. . 2023-10-00. Pubmed ID: 37769385; DOI: 10.1016/j.scr.2023.103214 ISTEMi001-AISTEMi002-AISTEMi003-A 2023-10-00 2023-10-00 PubMed: 37769385 DOI: 10.1016/j.scr.2023.103214Associated cell lines:
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Zhang Y, Liu Y, Yan W, Zhang X, Hou Y, Zhou Z, Guo R, Liu G, Ma J
Human induced pluripotent stem cell line from fibroblasts (HEBHMUi015-A) and chondrogenic differentiation
Zhang Y et al. Human induced pluripotent stem cell line from fibroblasts (HEBHMUi015-A) and chondrogenic differentiation. . 2023-10-00. Pubmed ID: 37856927; DOI: 10.1016/j.scr.2023.103201 HEBHMUi001-ACSUi004-AHEBHMUi015-A 2023-10-00 2023-10-00 PubMed: 37856927 DOI: 10.1016/j.scr.2023.103201Associated cell lines:
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Zhang M, Liu W, Li A, Htet MH, Yu R, Telli ML, Wu JC
Generation of two induced pluripotent stem cell lines from breast cancer patients carrying BRCA2 variants
Zhang M et al. Generation of two induced pluripotent stem cell lines from breast cancer patients carrying BRCA2 variants. . 2023-10-00. Pubmed ID: 37816281; DOI: 10.1016/j.scr.2023.103219; PMC: PMC10902209 SCVIi003-ASCVIi004-ASCVIi005-ASCVIi081-ASCVIi082-A 2023-10-00 2023-10-00 PubMed: 37816281 DOI: 10.1016/j.scr.2023.103219Associated cell lines:
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Zheng Ruixuan, Xu Tingting, Wang Xinghong, Yang Lehe, Wang Jian, Huang Xiaoying
Stem cell therapy in pulmonary hypertension: current practice and future opportunities
Zheng Ruixuan et al. Stem cell therapy in pulmonary hypertension: current practice and future opportunities. . 2023-09-30. DOI: 10.1183/16000617.0112-2023 PUMCHi003-A 2023-09-30 2023-09-30 DOI: 10.1183/16000617.0112-2023Associated cell lines:
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Wang X, Zhang H, Wang X, Zhou W, Dong L, Li N, He Q
Generation of an induced pluripotent stem cell line (SDASi001-A) from a Schimke immune-osseous dysplasia patient with SMARCAL1 mutations
Wang X et al. Generation of an induced pluripotent stem cell line (SDASi001-A) from a Schimke immune-osseous dysplasia patient with SMARCAL1 mutations. . 2023-10-00. Pubmed ID: 37788557; DOI: 10.1016/j.scr.2023.103217 SDASi001-A 2023-10-00 2023-10-00 PubMed: 37788557 DOI: 10.1016/j.scr.2023.103217Associated cell lines:
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Chen Yingji, Jiao Dongyue, Liu Yang, Xu Xiayun, Wang Yilin, Luo Xiaona, Saiyin Hexige, Li Yao, Gao Kun, Chen Yucai, Zhao Shi-Min, Ma Lixiang, Wang Chenji
FBXL4 mutations cause excessive mitophagy via BNIP3/BNIP3L accumulation leading to mitochondrial DNA depletion syndrome
Chen Yingji et al. FBXL4 mutations cause excessive mitophagy via BNIP3/BNIP3L accumulation leading to mitochondrial DNA depletion syndrome. . 2023-10-00. DOI: 10.1038/s41418-023-01205-1 SHCDNi001-A 2023-10-00 2023-10-00 DOI: 10.1038/s41418-023-01205-1Associated cell lines:
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Faruqui N, Williams DS, Briones A, Kepiro IE, Ravi J, Kwan TOC, Mearns-Spragg A, Ryadnov MG
Extracellular matrix type 0: From ancient collagen lineage to a versatile product pipeline - JellaGel™
Faruqui N et al. Extracellular matrix type 0: From ancient collagen lineage to a versatile product pipeline - JellaGel™. . 2023-10-00. Pubmed ID: 37692377; DOI: 10.1016/j.mtbio.2023.100786; PMC: PMC10491728 BIONi010-C 2023-10-00 2023-10-00 PubMed: 37692377 DOI: 10.1016/j.mtbio.2023.100786Associated cell lines:
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Grossmann Dajana, Malburg Nina, Glaß Hannes, Weeren Veronika, Sondermann Verena, Pfeiffer Julia F., Petters Janine, Lukas Jan, Seibler Philip, Klein Christine, Grünewald Anne, Hermann Andreas
Mitochondria–Endoplasmic Reticulum Contact Sites Dynamics and Calcium Homeostasis Are Differentially Disrupted in
Grossmann Dajana et al. Mitochondria–Endoplasmic Reticulum Contact Sites Dynamics and Calcium Homeostasis Are Differentially Disrupted inPINK1‐PD orPRKN‐PD NeuronsPINK1‐PD orPRKN‐PD Neurons. . 2023-10-00. DOI: 10.1002/mds.29525 AKOSi008-AAKOSi009-A 2023-10-00 2023-10-00 DOI: 10.1002/mds.29525Associated cell lines:
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Oleksy C, Massart F, Goldwurm S, Arado A, Arena G, Boussaad I, Krüger R
Generation and characterization of induced pluripotent stem cells from a Parkinson's disease patient carrying the digenic LRRK2 p.G2019S and GBA1 p.N409S mutations
Oleksy C et al. Generation and characterization of induced pluripotent stem cells from a Parkinson's disease patient carrying the digenic LRRK2 p.G2019S and GBA1 p.N409S mutations. . 2023-10-00. Pubmed ID: 37832355; DOI: 10.1016/j.scr.2023.103212 LCSBi013-A 2023-10-00 2023-10-00 PubMed: 37832355 DOI: 10.1016/j.scr.2023.103212Associated cell lines:
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Liu W, Zeng W, Kong X, Htet M, Yu R, Wheeler M, Day JW, Wu JC
Generation of two induced pluripotent stem cell lines from Duchenne muscular dystrophy patients
Liu W et al. Generation of two induced pluripotent stem cell lines from Duchenne muscular dystrophy patients. . 2023-10-00. Pubmed ID: 37740996; DOI: 10.1016/j.scr.2023.103207; PMC: PMC10949967 SCVIi087-ASCVIi088-A 2023-10-00 2023-10-00 PubMed: 37740996 DOI: 10.1016/j.scr.2023.103207Associated cell lines:
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Bonilauri B, Shin HS, Htet M, Yan CD, Witteles RM, Sallam K, Wu JC
Generation of two induced pluripotent stem cell lines from patients with cardiac amyloidosis carrying heterozygous transthyretin (TTR) mutation
Bonilauri B et al. Generation of two induced pluripotent stem cell lines from patients with cardiac amyloidosis carrying heterozygous transthyretin (TTR) mutation. . 2023-10-00. Pubmed ID: 37788558; DOI: 10.1016/j.scr.2023.103215; PMC: PMC10821799 SCVIi066-ASCVIi067-A 2023-10-00 2023-10-00 PubMed: 37788558 DOI: 10.1016/j.scr.2023.103215Associated cell lines:
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Begentas OC, Koc D, Sendur NK, Besarat P, Ezgin S, Temel M, Bora HAT, Kiris E
Generation and characterization of human induced pluripotent stem cell line METUi002-A from a patient with primary familial brain calcification (PFBC) carrying a heterozygous mutation (c.687dupT (p.Val230CysfsTer28)) in the SLC20A2 gene
Begentas OC et al. Generation and characterization of human induced pluripotent stem cell line METUi002-A from a patient with primary familial brain calcification (PFBC) carrying a heterozygous mutation (c.687dupT (p.Val230CysfsTer28)) in the SLC20A2 gene. . 2023-10-00. Pubmed ID: 37866220; DOI: 10.1016/j.scr.2023.103226 METUi002-A 2023-10-00 2023-10-00 PubMed: 37866220 DOI: 10.1016/j.scr.2023.103226Associated cell lines:
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Balducci V, Scardigli F, Harakalova M, Peter van Tintelen J, Doevendans PA, Costa KD, Turnbull IC, P G Sluijter J, Stillitano F
Generation and characterization of novel human induced pluripotent stem cell (iPSC) lines originating from five asymptomatic individuals carrying the PLN-R14del pathogenic variant and a non-carrier relative
Balducci V et al. Generation and characterization of novel human induced pluripotent stem cell (iPSC) lines originating from five asymptomatic individuals carrying the PLN-R14del pathogenic variant and a non-carrier relative. . 2023-10-00. Pubmed ID: 37748331; DOI: 10.1016/j.scr.2023.103208 ISMMSi052-AISMMSi053-AISMMSi054-AISMMSi056-AISMMSi057-AISMMSi058-A 2023-10-00 2023-10-00 PubMed: 37748331 DOI: 10.1016/j.scr.2023.103208Associated cell lines:
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Sanjurjo-Soriano Carla, Jimenez-Medina Carla, Erkilic Nejla, Cappellino Luisina, Lefevre Arnaud, Nagel-Wolfrum Kerstin, Wolfrum Uwe, Van Wijk Erwin, Roux Anne-Françoise, Meunier Isabelle, Kalatzis Vasiliki
USH2A variants causing retinitis pigmentosa or Usher syndrome provoke differential retinal phenotypes in disease-specific organoids
Sanjurjo-Soriano Carla et al. USH2A variants causing retinitis pigmentosa or Usher syndrome provoke differential retinal phenotypes in disease-specific organoids. . 2023-10-00. DOI: 10.1016/j.xhgg.2023.100229 INMi001-AINMi002-AINMi005-A 2023-10-00 2023-10-00 DOI: 10.1016/j.xhgg.2023.100229 -
Stanberry I, Cunningham D, Ye S, Alonzo M, Zhao MT, Garg V, Lilly B
Characterization of an induced pluripotent stem cell line NCHi011-A from a 23-year-old female with Alagille Syndrome harboring a heterozygous JAG1 pathogenic variant
Stanberry I et al. Characterization of an induced pluripotent stem cell line NCHi011-A from a 23-year-old female with Alagille Syndrome harboring a heterozygous JAG1 pathogenic variant. . 2023-10-00. Pubmed ID: 37774637; DOI: 10.1016/j.scr.2023.103213; PMC: PMC10807224 NCHi011-A 2023-10-00 2023-10-00 PubMed: 37774637 DOI: 10.1016/j.scr.2023.103213Associated cell lines:
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Molugu K, Khajanchi N, Lazzarotto CR, Tsai SQ, Saha K
Trichostatin A for Efficient CRISPR-Cas9 Gene Editing of Human Pluripotent Stem Cells
Molugu K et al. Trichostatin A for Efficient CRISPR-Cas9 Gene Editing of Human Pluripotent Stem Cells. . 2023-10-00. Pubmed ID: 37676985; DOI: 10.1089/crispr.2023.0033; PMC: PMC10611976 UCSFi001-A-28 2023-10-00 2023-10-00 PubMed: 37676985 DOI: 10.1089/crispr.2023.0033Associated cell lines:
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Zhu W, Liu W, Yu R, Manning M, Waran Romfh A, Wu JC
Generation of two induced pluripotent stem cell lines from patients with Down syndrome
Zhu W et al. Generation of two induced pluripotent stem cell lines from patients with Down syndrome. . 2023-10-00. Pubmed ID: 37734318; DOI: 10.1016/j.scr.2023.103204; PMC: PMC10802983 SCVIi001-ASCVIi002-ASCVIi085-ASCVIi086-A 2023-10-00 2023-10-00 PubMed: 37734318 DOI: 10.1016/j.scr.2023.103204Associated cell lines:
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Hongmei G, Xiaofang S, Bing S
Establishment of human-induced pluripotent stem cell GZHMCi0011-A from peripheral blood mononuclear cells from a volunteer with 14/63 CAG repeats of the ATXN3 mutation
Hongmei G et al. Establishment of human-induced pluripotent stem cell GZHMCi0011-A from peripheral blood mononuclear cells from a volunteer with 14/63 CAG repeats of the ATXN3 mutation. . 2023-10-00. Pubmed ID: 37866221; DOI: 10.1016/j.scr.2023.103190 GZHMCi011-A 2023-10-00 2023-10-00 PubMed: 37866221 DOI: 10.1016/j.scr.2023.103190Associated cell lines:
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Xu P, Guo F, Xiao W, Wang Y, Ye K, Mao Y, Zhong X
Generation and characterization of two induced pluripotent stem cell lines from conjunctiva of a retinoblastoma patient
Xu P et al. Generation and characterization of two induced pluripotent stem cell lines from conjunctiva of a retinoblastoma patient. . 2023-10-00. Pubmed ID: 37708614; DOI: 10.1016/j.scr.2023.103200 SKLOi004-ASKLOi004-B 2023-10-00 2023-10-00 PubMed: 37708614 DOI: 10.1016/j.scr.2023.103200Associated cell lines:
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Caillaud A, Bray L, Girardeau A, Begué-Racapé Z, Vince L, Patitucci M, Le May C, Lambert G, Cariou B, Rimbert A
Generation of an induced pluripotent stem cell line (ITXi012-A) from a patient with genetically determined high-lipoprotein(a) plasma levels
Caillaud A et al. Generation of an induced pluripotent stem cell line (ITXi012-A) from a patient with genetically determined high-lipoprotein(a) plasma levels. . 2023-10-00. Pubmed ID: 37734317; DOI: 10.1016/j.scr.2023.103205 ITXi001-AITXi001-A-1ITXi012-A 2023-10-00 2023-10-00 PubMed: 37734317 DOI: 10.1016/j.scr.2023.103205Associated cell lines:
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Leng Yubing, Li Xiaorui, Zheng Fuyin, Liu Hui, Wang Chunyan, Wang Xudong, Liao Yulong, Liu Jiangyue, Meng Kaiqi, Yu Jiaheng, Zhang Jingyi, Wang Binyu, Tan Yingjun, Liu Meili, Jia Xiaoling, Li Deyu, Li Yinghui, Gu Zhongze, Fan Yubo
Advances in In Vitro Models of Neuromuscular Junction: Focusing on Organ‐on‐a‐Chip, Organoids, and Biohybrid Robotics
Leng Yubing et al. Advances in In Vitro Models of Neuromuscular Junction: Focusing on Organ‐on‐a‐Chip, Organoids, and Biohybrid Robotics. . 2023-10-00. DOI: 10.1002/adma.202211059 CHUQi001-A 2023-10-00 2023-10-00 DOI: 10.1002/adma.202211059Associated cell lines:
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Chen G, Orozco L, Parmisano S, Jahng JWS, Vera CD, Zhuge Y, Wu JC, Obal D
Generation of two induced pluripotent stem cell lines from patients suffering from pulmonary hypertension
Chen G et al. Generation of two induced pluripotent stem cell lines from patients suffering from pulmonary hypertension. . 2023-10-00. Pubmed ID: 37804546; DOI: 10.1016/j.scr.2023.103218; PMC: PMC11006094 SCVIi079-ASCVIi080-A 2023-10-00 2023-10-00 PubMed: 37804546 DOI: 10.1016/j.scr.2023.103218Associated cell lines:
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Goual L, Bounasri E, Vincenti M, Amédro P, Desprat R, Bernex F, Lemaitre JM, Pasquié JL, Lacampagne A, Thireau J, Meli AC
Generation of patient-specific induced pluripotent stem cell lines with Type 2 Long QT Syndrome and the KCNH2 c.379C > T pathogenic variant
Goual L et al. Generation of patient-specific induced pluripotent stem cell lines with Type 2 Long QT Syndrome and the KCNH2 c.379C > T pathogenic variant. . 2023-10-00. Pubmed ID: 37660555; DOI: 10.1016/j.scr.2023.103192 INSRMi014-AINSRMi015-A 2023-10-00 2023-10-00 PubMed: 37660555 DOI: 10.1016/j.scr.2023.103192Associated cell lines:
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Chae CW, Yoon JH, Lim JR, Park JY, Cho JH, Jung YH, Choi GE, Lee HJ, Han HJ
TRIM16-mediated lysophagy suppresses high-glucose-accumulated neuronal Aβ
Chae CW et al. TRIM16-mediated lysophagy suppresses high-glucose-accumulated neuronal Aβ. . 2023-10-00. Pubmed ID: 37357416; DOI: 10.1080/15548627.2023.2229659; PMC: PMC10472864 KSCBi005-A 2023-10-00 2023-10-00 PubMed: 37357416 DOI: 10.1080/15548627.2023.2229659Associated cell lines:
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Chatrousse L, Poullion T, El-Kassar L, Giraud-Triboult K, Boissart C, Sanatine P, Sommer P, Benchoua A
Establishment of heterozygous and homozygous SHANK3 knockout clonal pluripotent stem cells from the parental hESC line SA001 using CRISPR/Cas9
Chatrousse L et al. Establishment of heterozygous and homozygous SHANK3 knockout clonal pluripotent stem cells from the parental hESC line SA001 using CRISPR/Cas9. . 2023-10-00. Pubmed ID: 37769384; DOI: 10.1016/j.scr.2023.103209 CEBe033-A-2CEBe033-A-3CEBe033-A-4CEBe033-A-5CEBe033-A-6CEBe033-A-7 2023-10-00 2023-10-00 PubMed: 37769384 DOI: 10.1016/j.scr.2023.103209Associated cell lines:
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Kirkeby Agnete, Nelander Jenny, Hoban Deirdre B., Rogelius Nina, Bjartmarz Hjálmar, Storm Petter, Fiorenzano Alessandro, Adler Andrew F., Vale Shelby, Mudannayake Janitha, Zhang Yu, Cardoso Tiago, Mattsson Bengt, Landau Anne M., Glud Andreas N., Sørensen Jens C., Lillethorup Thea P., Lowdell Mark, Carvalho Carla, Bain Owen, van Vliet Trinette, Lindvall Olle, Björklund Anders, Harry Bronwen, Cutting Emma, Widner Håkan, Paul Gesine, Barker Roger A., Parmar Malin
Preclinical quality, safety, and efficacy of a human embryonic stem cell-derived product for the treatment of Parkinson’s disease, STEM-PD
Kirkeby Agnete et al. Preclinical quality, safety, and efficacy of a human embryonic stem cell-derived product for the treatment of Parkinson’s disease, STEM-PD. . 2023-10-00. DOI: 10.1016/j.stem.2023.08.014 RCe021-A 2023-10-00 2023-10-00 DOI: 10.1016/j.stem.2023.08.014Associated cell lines:
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Provost CC, Auboyer L, Rovelet-Lecrux A, Monzo C, Schob E, Lehmann S, Wallon D, Crozet C
Establishment of induced pluripotent stem cells IRMBi005-A from a patient with sporadic Alzheimer's disease
Provost CC et al. Establishment of induced pluripotent stem cells IRMBi005-A from a patient with sporadic Alzheimer's disease. . 2023-10-00. Pubmed ID: 37783001; DOI: 10.1016/j.scr.2023.103216 IRMBi005-A 2023-10-00 2023-10-00 PubMed: 37783001 DOI: 10.1016/j.scr.2023.103216Associated cell lines:
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De Serres-Bérard T, Jauvin D, Puymirat J, Chahine M
Generation of induced pluripotent stem cell lines from pediatric patients with congenital myotonic dystrophy (CBRCULi012-A and CBRCULi013-A) and age-matched controls (CBRCULi010-A and CBRCULi011-A)
De Serres-Bérard T et al. Generation of induced pluripotent stem cell lines from pediatric patients with congenital myotonic dystrophy (CBRCULi012-A and CBRCULi013-A) and age-matched controls (CBRCULi010-A and CBRCULi011-A). . 2023-10-00. Pubmed ID: 37871474; DOI: 10.1016/j.scr.2023.103234 CBRCULi001-ACBRCULi002-ACBRCULi003-ACBRCULi004-ACBRCULi005-ACBRCULi010-ACBRCULi011-ACBRCULi012-ACBRCULi013-A 2023-10-00 2023-10-00 PubMed: 37871474 DOI: 10.1016/j.scr.2023.103234Associated cell lines:
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Dębczyński M, Mojsak D, Tamburro S, Baldassari S, Musante I, Casciaro R, Ciciriello F, Zara F, Scudieri P, Gorrieri G
Generation of an induced pluripotent stem cell line (IGGi002A) from nasal cells of a cystic fibrosis patient homozygous for the G542X-CFTR mutation
Dębczyński M et al. Generation of an induced pluripotent stem cell line (IGGi002A) from nasal cells of a cystic fibrosis patient homozygous for the G542X-CFTR mutation. . 2023-10-00. Pubmed ID: 37865062; DOI: 10.1016/j.scr.2023.103232 IGGi002-A 2023-10-00 2023-10-00 PubMed: 37865062 DOI: 10.1016/j.scr.2023.103232Associated cell lines:
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Jiang H, Xu C, Li W, Zhou L, Fang F
Generation of an induced pluripotent stem cell line (BCHNCi003-A) from a patient with mitochondrial pyruvate carrier deficiency caused by biallelic MPC1 mutations
Jiang H et al. Generation of an induced pluripotent stem cell line (BCHNCi003-A) from a patient with mitochondrial pyruvate carrier deficiency caused by biallelic MPC1 mutations. . 2023-10-00. Pubmed ID: 37769383; DOI: 10.1016/j.scr.2023.103206 BCHNCi003-A 2023-10-00 2023-10-00 PubMed: 37769383 DOI: 10.1016/j.scr.2023.103206Associated cell lines:
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She L, Li X, Bai M
Generation of an induced pluripotent stem cell line XJHi001-A from a fibronectin glomerulopathy patient carrying a heterozygous NM_212482.2(C.5888-1G > C) mutation in the FN1 gene
She L et al. Generation of an induced pluripotent stem cell line XJHi001-A from a fibronectin glomerulopathy patient carrying a heterozygous NM_212482.2(C.5888-1G > C) mutation in the FN1 gene. . 2023-10-00. Pubmed ID: 37801747; DOI: 10.1016/j.scr.2023.103203 XJHi001-A 2023-10-00 2023-10-00 PubMed: 37801747 DOI: 10.1016/j.scr.2023.103203Associated cell lines:
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Takasaki K, Kumar SS, Gagne A, French DL, Chou ST
Generation of CHOPi-008-B, a euploid iPSC line from a patient with Trisomy 21 and a GATA1 mutation
Takasaki K et al. Generation of CHOPi-008-B, a euploid iPSC line from a patient with Trisomy 21 and a GATA1 mutation. . 2023-10-00. Pubmed ID: 37677872; DOI: 10.1016/j.scr.2023.103198; PMC: PMC10872805 SCSe001-ACHOPi002-ACHOPi003-ASCSe001-A-3CHOPi008-ACHOPi008-BCHOPi008-C 2023-10-00 2023-10-00 PubMed: 37677872 DOI: 10.1016/j.scr.2023.103198Associated cell lines:
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Zanuttigh E, Rusha E, Peron C, Brunetti D, Zorzi G, Pertek A, Nteli P, Winkelmann J, Tiranti V, Iuso A
Generation of two human iPSC lines, HMGUi004-A and FINCBi004-A, from fibroblasts of MPAN patients carrying pathogenic recessive mutations in the gene C19orf12
Zanuttigh E et al. Generation of two human iPSC lines, HMGUi004-A and FINCBi004-A, from fibroblasts of MPAN patients carrying pathogenic recessive mutations in the gene C19orf12. . 2023-10-00. Pubmed ID: 37689041; DOI: 10.1016/j.scr.2023.103197 HMGUi004-AFINCBi004-A 2023-10-00 2023-10-00 PubMed: 37689041 DOI: 10.1016/j.scr.2023.103197Associated cell lines:
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Han HJ, Kim JH
KSCBi005-A-8(hiPSC-PD-L1KO), a PD-L1 knockout human induced pluripotent stem cell line for demonstrating the role of the PD-1/PD-L1 axis
Han HJ et al. KSCBi005-A-8(hiPSC-PD-L1KO), a PD-L1 knockout human induced pluripotent stem cell line for demonstrating the role of the PD-1/PD-L1 axis. . 2023-10-00. Pubmed ID: 37690432; DOI: 10.1016/j.scr.2023.103196 KSCBi005-AKSCBi005-A-8 2023-10-00 2023-10-00 PubMed: 37690432 DOI: 10.1016/j.scr.2023.103196Associated cell lines:
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Daya NM, Mavrommatis L, Zhuge H, Athamneh M, Roos A, Gläser D, Doering K, Zaehres H, Vorgerd M, Güttsches AK
Generation of a human iPSC line (HIMRi001-A) from a patient with filaminopathy
Daya NM et al. Generation of a human iPSC line (HIMRi001-A) from a patient with filaminopathy. . 2023-10-00. Pubmed ID: 37748332; DOI: 10.1016/j.scr.2023.103210 HIMRi001-A 2023-10-00 2023-10-00 PubMed: 37748332 DOI: 10.1016/j.scr.2023.103210Associated cell lines:
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Boeing A, Mavrommatis L, Daya NM, Zhuge H, Volke L, Kocabas A, Kneifel M, Athamneh M, Krause K, Südkamp N, Döring K, Theiss C, Roos A, Zaehres H, Güttsches AK, Vorgerd M
Generation of two human iPSC lines (HIMRi002-A and HIMRi003-A) derived from Caveolinopathy patients with rippling muscle disease
Boeing A et al. Generation of two human iPSC lines (HIMRi002-A and HIMRi003-A) derived from Caveolinopathy patients with rippling muscle disease. . 2023-10-00. Pubmed ID: 37839261; DOI: 10.1016/j.scr.2023.103220 HIMRi002-AHIMRi003-A 2023-10-00 2023-10-00 PubMed: 37839261 DOI: 10.1016/j.scr.2023.103220Associated cell lines:
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Shen M, Fan S, Wu F, Cheng P, Gao Y, Zheng P, Feng S, Ji X, Chen Q, Zhang X
Generation of a human iPSC line CIPi003-A from a patient with focal epilepsy harboring a heterozygous mutation in DEPDC5 gene
Shen M et al. Generation of a human iPSC line CIPi003-A from a patient with focal epilepsy harboring a heterozygous mutation in DEPDC5 gene. . 2023-10-00. Pubmed ID: 37722146; DOI: 10.1016/j.scr.2023.103195 CIPi003-A 2023-10-00 2023-10-00 PubMed: 37722146 DOI: 10.1016/j.scr.2023.103195Associated cell lines:
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Cao Y, Tang L, Su J, Wang H, Liang P, Rong K, Gong T
Generation of a TRPV1 knockout human pluripotent stem cell line (WAe009-A-U) using CRISPR/Cas9
Cao Y et al. Generation of a TRPV1 knockout human pluripotent stem cell line (WAe009-A-U) using CRISPR/Cas9. . 2023-10-00. Pubmed ID: 37708613; DOI: 10.1016/j.scr.2023.103202 WAe009-AWAe009-A-U 2023-10-00 2023-10-00 PubMed: 37708613 DOI: 10.1016/j.scr.2023.103202Associated cell lines:
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Laowtammathron C, Lorthongpanich C, Jiamvoraphong N, Srisook P, Klaihmon P, Kheolamai P, Luanpitpong S, Issaragrisil S
Role of YAP in hematopoietic differentiation and erythroid lineage specification of human-induced pluripotent stem cells
Laowtammathron C et al. Role of YAP in hematopoietic differentiation and erythroid lineage specification of human-induced pluripotent stem cells. . 2023-09-29. Pubmed ID: 37775798; DOI: 10.1186/s13287-023-03508-z; PMC: PMC10543272 MUSIe001-AMUSIi012-AMUSIi012-A-1MUSIi012-A-2MUSIi012-A-3MUSIi012-A-4MUSIi017-AMUSIi017-A-1MUSIi017-A-2MUSIi012-A-5 2023-09-29 2023-09-29 PubMed: 37775798 DOI: 10.1186/s13287-023-03508-zAssociated cell lines:
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Menduti G, Boido M
Recent Advances in High-Content Imaging and Analysis in iPSC-Based Modelling of Neurodegenerative Diseases
Menduti G et al. Recent Advances in High-Content Imaging and Analysis in iPSC-Based Modelling of Neurodegenerative Diseases. . 2023-09-28. Pubmed ID: 37834135; DOI: 10.3390/ijms241914689; PMC: PMC10572296 BIHi005-ABIHi005-A-24 2023-09-28 2023-09-28 PubMed: 37834135 DOI: 10.3390/ijms241914689Associated cell lines:
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Chen Chao, Guan Min-Xin
Induced pluripotent stem cells: ex vivo models for human diseases due to mitochondrial DNA mutations
Chen Chao et al. Induced pluripotent stem cells: ex vivo models for human diseases due to mitochondrial DNA mutations. . 2023-09-22. DOI: 10.1186/s12929-023-00967-7 FINCBi001-AUOMi005-A 2023-09-22 2023-09-22 DOI: 10.1186/s12929-023-00967-7Associated cell lines:
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Eremeev Artem, Pikina Arina, Ruchko Yevgeny, Bogomazova Alexandra
Clinical Potential of Cellular Material Sources in the Generation of iPSC-Based Products for the Regeneration of Articular Cartilage
Eremeev Artem et al. Clinical Potential of Cellular Material Sources in the Generation of iPSC-Based Products for the Regeneration of Articular Cartilage. . 2023-09-22. DOI: 10.3390/ijms241914408 SHFDi001-ADMBi003-ADMBi004-A 2023-09-22 2023-09-22 DOI: 10.3390/ijms241914408Associated cell lines:
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Mazarico-Altisent Isabel, Capel Ismael, Baena Neus, Bella-Cueto Maria Rosa, Barcons Santi, Guirao Xavier, Pareja Rocío, Muntean Andreea, Arsentales Valeria, Caixàs Assumpta, Rigla Mercedes
Genetic testing for familial hyperparathyroidism: clinical-genetic profile in a Mediterranean cohort
Mazarico-Altisent Isabel et al. Genetic testing for familial hyperparathyroidism: clinical-genetic profile in a Mediterranean cohort. . 2023-09-21. DOI: 10.3389/fendo.2023.1244361 CSSi015-A 2023-09-21 2023-09-21 DOI: 10.3389/fendo.2023.1244361Associated cell lines:
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Lim SW, Na D, Lee H, Fang X, Cui S, Shin YJ, Lee KI, Lee JY, Yang CW, Chung BH
Modeling of FAN1-Deficient Kidney Disease Using a Human Induced Pluripotent Stem Cell-Derived Kidney Organoid System
Lim SW et al. Modeling of FAN1-Deficient Kidney Disease Using a Human Induced Pluripotent Stem Cell-Derived Kidney Organoid System. . 2023-09-20. Pubmed ID: 37759541; DOI: 10.3390/cells12182319; PMC: PMC10529520 CMCi001-ACMCi002-ACMCi006-ACMCi007-A 2023-09-20 2023-09-20 PubMed: 37759541 DOI: 10.3390/cells12182319 -
Otero MG, Bell S, Laperle AH, Lawless G, Myers Z, Castro MA, Villalba JM, Svendsen CN
Organ-Chips Enhance the Maturation of Human iPSC-Derived Dopamine Neurons
Otero MG et al. Organ-Chips Enhance the Maturation of Human iPSC-Derived Dopamine Neurons. . 2023-09-18. Pubmed ID: 37762529; DOI: 10.3390/ijms241814227; PMC: PMC10531789 EDi044-A 2023-09-18 2023-09-18 PubMed: 37762529 DOI: 10.3390/ijms241814227Associated cell lines:
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Foerster Leo Carl, Kaya Oguzhan, Wüst Valentin, Bekavac Milica, Ziegler Kevin Chris, Akcay Vuslat, Stinchcombe Nina, Gesteira Perez Noelia, Ma Xiujian, Sadik Ahmed, Le Phuong Uyen, Petrecca Kevin, Opitz Christiane, Liu Haikun, Wirtz Christian Rainer, Anders Simon, Goncalves Angela, Martin-Villalba Ana
Identification of astrocyte-driven pseudolineages reveals clinical stratification and therapeutic targets in Glioblastoma
Foerster Leo Carl et al. Identification of astrocyte-driven pseudolineages reveals clinical stratification and therapeutic targets in Glioblastoma. . 2023-09-17. DOI: 10.1101/2023.09.15.557713 UCSFi001-A 2023-09-17 2023-09-17 DOI: 10.1101/2023.09.15.557713Associated cell lines:
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Ludwik KA, Telugu N, Schommer S, Stachelscheid H, Diecke S
ASSURED-optimized CRISPR protocol for knockout/SNP knockin in hiPSCs
Ludwik KA et al. ASSURED-optimized CRISPR protocol for knockout/SNP knockin in hiPSCs. . 2023-09-15. Pubmed ID: 37481731; DOI: 10.1016/j.xpro.2023.102406; PMC: PMC10382939 BIHi005-A 2023-09-15 2023-09-15 PubMed: 37481731 DOI: 10.1016/j.xpro.2023.102406Associated cell lines:
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Li Chong, Fleck Jonas Simon, Martins-Costa Catarina, Burkard Thomas R., Themann Jan, Stuempflen Marlene, Peer Angela Maria, Vertesy Ábel, Littleboy Jamie B., Esk Christopher, Elling Ulrich, Kasprian Gregor, Corsini Nina S., Treutlein Barbara, Knoblich Juergen A.
Single-cell brain organoid screening identifies developmental defects in autism
Li Chong et al. Single-cell brain organoid screening identifies developmental defects in autism. . 2023-09-14. DOI: 10.1038/s41586-023-06473-y IMBAi016-AIMBAi017-AIMBAi017-A-1IMBAi017-A-2 2023-09-14 2023-09-14 DOI: 10.1038/s41586-023-06473-yAssociated cell lines:
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Liu Xianlin, Wen Jie, Liu Xuezhong, Chen Anhai, Li Sijun, Liu Jing, Sun Jie, Gong Wei, Kang Xiaoming, Feng Zhili, He Chufeng, Mei Lingyun, Ling Jie, Feng Yong
Gene regulation analysis of patient-derived iPSCs and its CRISPR-corrected control provides a new tool for studying perturbations of ELMOD3 c.512A>G mutation during the development of inherited hearing loss
Liu Xianlin et al. Gene regulation analysis of patient-derived iPSCs and its CRISPR-corrected control provides a new tool for studying perturbations of ELMOD3 c.512A>G mutation during the development of inherited hearing loss. . 2023-09-14. DOI: 10.1371/journal.pone.0288640 CSUXHi003-A 2023-09-14 2023-09-14 DOI: 10.1371/journal.pone.0288640Associated cell lines:
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Pranty Abida Islam, Wruck Wasco, Adjaye James
Free Bilirubin Induces Neuro-Inflammation in an Induced Pluripotent Stem Cell-Derived Cortical Organoid Model of Crigler-Najjar Syndrome
Pranty Abida Islam et al. Free Bilirubin Induces Neuro-Inflammation in an Induced Pluripotent Stem Cell-Derived Cortical Organoid Model of Crigler-Najjar Syndrome. . 2023-09-14. DOI: 10.3390/cells12182277 HHUUKDi005-A 2023-09-14 2023-09-14 DOI: 10.3390/cells12182277Associated cell lines:
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Han CZ, Li RZ, Hansen E, Trescott S, Fixsen BR, Nguyen CT, Mora CM, Spann NJ, Bennett HR, Poirion O, Buchanan J, Warden AS, Xia B, Schlachetzki JCM, Pasillas MP, Preissl S, Wang A, O'Connor C, Shriram S, Kim R, Schafer D, Ramirez G, Challacombe J, Anavim SA, Johnson A, Gupta M, Glass IA, Birth Defects Research Laboratory, Levy ML, Haim SB, Gonda DD, Laurent L, Hughes JF, Page DC, Blurton-Jones M, Glass CK, Coufal NG
Human microglia maturation is underpinned by specific gene regulatory networks
Han CZ et al. Human microglia maturation is underpinned by specific gene regulatory networks. . 2023-09-12. Pubmed ID: 37582369; DOI: 10.1016/j.immuni.2023.07.016; PMC: PMC10529991 WAe001-A 2023-09-12 2023-09-12 PubMed: 37582369 DOI: 10.1016/j.immuni.2023.07.016Associated cell lines:
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Lima Cunha D, Sarkar H, Eintracht J, Harding P, Zhou JH, Moosajee M
Restoration of functional PAX6 in aniridia patient iPSC-derived ocular tissue models using repurposed nonsense suppression drugs
Lima Cunha D et al. Restoration of functional PAX6 in aniridia patient iPSC-derived ocular tissue models using repurposed nonsense suppression drugs. . 2023-09-12. Pubmed ID: 37483273; DOI: 10.1016/j.omtn.2023.06.016; PMC: PMC10362734 WAe009-AUCLi013-AUCLi016-AUCLi017-A 2023-09-12 2023-09-12 PubMed: 37483273 DOI: 10.1016/j.omtn.2023.06.016 -
Souralova T, Hulinova D, Jeseta M, Ventruba P, Hampl A, Koutna I
Truncated vitronectin with E-cadherin enables the xeno-free derivation of human embryonic stem cells
Souralova T et al. Truncated vitronectin with E-cadherin enables the xeno-free derivation of human embryonic stem cells. . 2023-09-12. Pubmed ID: 37700192; DOI: 10.1038/s41598-023-42236-5; PMC: PMC10497536 CTEFe001-ACTEFe002-ACTEFe003-AMUNIe010-AMUNIe011-AMUNIe012-A 2023-09-12 2023-09-12 PubMed: 37700192 DOI: 10.1038/s41598-023-42236-5Associated cell lines:
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Buck TM, Quinn PMJ, Pellissier LP, Mulder AA, Jongejan A, Lu X, Boon N, Koot D, Almushattat H, Arendzen CH, Vos RM, Bradley EJ, Freund C, Mikkers HMM, Boon CJF, Moerland PD, Baas F, Koster AJ, Neefjes J, Berlin I, Jost CR, Wijnholds J
CRB1 is required for recycling by RAB11A+ vesicles in human retinal organoids
Buck TM et al. CRB1 is required for recycling by RAB11A+ vesicles in human retinal organoids. . 2023-09-12. Pubmed ID: 37541258; DOI: 10.1016/j.stemcr.2023.07.001; PMC: PMC10545476 LUMCi029-BLUMCi055-ALUMCi056-ALUMCi054-A-2LUMCi056-A-1 2023-09-12 2023-09-12 PubMed: 37541258 DOI: 10.1016/j.stemcr.2023.07.001Associated cell lines:
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Chowdhury A, Boshnakovska A, Aich A, Methi A, Vergel Leon AM, Silbern I, Lüchtenborg C, Cyganek L, Prochazka J, Sedlacek R, Lindovsky J, Wachs D, Nichtova Z, Zudova D, Koubkova G, Fischer A, Urlaub H, Brügger B, Katschinski DM, Dudek J, Rehling P
Metabolic switch from fatty acid oxidation to glycolysis in knock-in mouse model of Barth syndrome
Chowdhury A et al. Metabolic switch from fatty acid oxidation to glycolysis in knock-in mouse model of Barth syndrome. . 2023-09-11. Pubmed ID: 37533404; DOI: 10.15252/emmm.202317399; PMC: PMC10493589 UMGi054-AUMGi014-C 2023-09-11 2023-09-11 PubMed: 37533404 DOI: 10.15252/emmm.202317399 -
Uzbas F, O'Neill AC
Spatial Centrosome Proteomic Profiling of Human iPSC-derived Neural Cells
Uzbas F et al. Spatial Centrosome Proteomic Profiling of Human iPSC-derived Neural Cells. . 2023-09-05. Pubmed ID: 37727868; DOI: 10.21769/bioprotoc.4812; PMC: PMC10505934 ISFi001-AISFi002-A 2023-09-05 2023-09-05 PubMed: 37727868 DOI: 10.21769/bioprotoc.4812 -
Pohl Katherine A., Zhang Xiangmei, Pham Anh H., Chan Jane W., Sadun Alfredo A., Yang Xian-Jie
Establishing induced pluripotent stem cell lines from two dominant optic atrophy patients with distinct OPA1 mutations and clinical pathologies
Pohl Katherine A. et al. Establishing induced pluripotent stem cell lines from two dominant optic atrophy patients with distinct OPA1 mutations and clinical pathologies. . 2023-09-04. DOI: 10.3389/fgene.2023.1251216 IISHDOi003-ABIOi002-APUMCHi019-A 2023-09-04 2023-09-04 DOI: 10.3389/fgene.2023.1251216Associated cell lines:
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Sánchez-Duffhues Gonzalo, Hiepen Christian
Human iPSCs as Model Systems for BMP-Related Rare Diseases
Sánchez-Duffhues Gonzalo et al. Human iPSCs as Model Systems for BMP-Related Rare Diseases. . 2023-09-02. DOI: 10.3390/cells12172200 KMUGMCi001-A 2023-09-02 2023-09-02 DOI: 10.3390/cells12172200Associated cell lines:
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Devito LG, Zanjani ZS, Evans JR, Scardamaglia A, Houlden H, Gandhi S, Healy L
Generation of TWO G51D SNCA missense mutation iPSC lines (CRICKi011-A, CRICKi012-A) from two individuals at risk of Parkinson's disease
Devito LG et al. Generation of TWO G51D SNCA missense mutation iPSC lines (CRICKi011-A, CRICKi012-A) from two individuals at risk of Parkinson's disease. . 2023-09-00. Pubmed ID: 37336145; DOI: 10.1016/j.scr.2023.103134 CRICKi001-ACRICKi011-ACRICKi012-A 2023-09-00 2023-09-00 PubMed: 37336145 DOI: 10.1016/j.scr.2023.103134Associated cell lines:
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Alowaysi M, Al-Shehri M, Baadhaim M, AlZahrani H, Aboalola D, Daghestani M, Hashem H, Aljahdali R, Salem R, Alharbi A, Muharraq M, Alghamdi K, Alsobiy F, Zia A, Lehmann R, Tegner J, Alsayegh K
Generation of myoglobin (MB)-knockout human embryonic stem cell (hESC) line (KAIMRCe002-A-1S) using CRISPR/Cas9 technology
Alowaysi M et al. Generation of myoglobin (MB)-knockout human embryonic stem cell (hESC) line (KAIMRCe002-A-1S) using CRISPR/Cas9 technology. . 2023-09-00. Pubmed ID: 37406498; DOI: 10.1016/j.scr.2023.103158 WAe001-A-1S 2023-09-00 2023-09-00 PubMed: 37406498 DOI: 10.1016/j.scr.2023.103158Associated cell lines:
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Li H, Zhang B, Shi Z, Wu H, Mei S, Ai T, Shi A, Wang L, Zhu M, Tang J
Derivation of induced pluripotent stem cell SJTUi003-A from a 69-year-old Chinese Han Sporadic Alzheimer's disease patient with APOEε3/ε4 genetic background
Li H et al. Derivation of induced pluripotent stem cell SJTUi003-A from a 69-year-old Chinese Han Sporadic Alzheimer's disease patient with APOEε3/ε4 genetic background. . 2023-09-00. Pubmed ID: 37343430; DOI: 10.1016/j.scr.2023.103142 SJTUi003-A 2023-09-00 2023-09-00 PubMed: 37343430 DOI: 10.1016/j.scr.2023.103142Associated cell lines:
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Lu F, Gao Y, Li E
Generation of a FLNA knockout hESC line (WAe009-A-P) to model cardiac valvular dysplasia using CRISPR/Cas9
Lu F et al. Generation of a FLNA knockout hESC line (WAe009-A-P) to model cardiac valvular dysplasia using CRISPR/Cas9. . 2023-09-00. Pubmed ID: 37429070; DOI: 10.1016/j.scr.2023.103162 WAe009-AZZUNEUi008-AWAe009-A-P 2023-09-00 2023-09-00 PubMed: 37429070 DOI: 10.1016/j.scr.2023.103162Associated cell lines:
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Rajendran Meenakshi Sundari, Prabhakaran Rajkumar, Muthaiyan Ahalliya Rathi, Muthusami Sridhar, Kannappan Poornima, Vani Raju Manikandan, Kaniyur Chandrasekaran Meenakshi
Neuronal wires and novel epileptic gene studies: Methods and mechanism of brain network and - Recent update
Rajendran Meenakshi Sundari et al. Neuronal wires and novel epileptic gene studies: Methods and mechanism of brain network and - Recent update. . 2023-09-00. DOI: 10.1016/j.humgen.2023.201186 OGHFUi001-A 2023-09-00 2023-09-00 DOI: 10.1016/j.humgen.2023.201186Associated cell lines:
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Yu Y, Alonzo M, Ye S, Fang A, Manickam K, Garg V, Zhao MT
Generation of an induced pluripotent stem cell line (NCHi010-A) from a 6-year-old female with Down syndrome and without congenital heart disease
Yu Y et al. Generation of an induced pluripotent stem cell line (NCHi010-A) from a 6-year-old female with Down syndrome and without congenital heart disease. . 2023-09-00. Pubmed ID: 37392705; DOI: 10.1016/j.scr.2023.103155; PMC: PMC10530593 NCHi010-A 2023-09-00 2023-09-00 PubMed: 37392705 DOI: 10.1016/j.scr.2023.103155Associated cell lines:
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Takahashi M
Generation of a human induced pluripotent stem cell line harboring the infant leukemia-associated fusion gene, KMT2A-AFF1 (IMSUTi002-A-2)
Takahashi M. Generation of a human induced pluripotent stem cell line harboring the infant leukemia-associated fusion gene, KMT2A-AFF1 (IMSUTi002-A-2). . 2023-09-00. Pubmed ID: 37639801; DOI: 10.1016/j.scr.2023.103185 IMSUTi002-AIMSUTi002-A-1IMSUTi002-A-2 2023-09-00 2023-09-00 PubMed: 37639801 DOI: 10.1016/j.scr.2023.103185Associated cell lines:
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Grigor'eva EV, Malakhova AA, Ghukasyan L, Hayrapetyan V, Atshemyan S, Vardanyan V, Zakian SM, Zakharyan R, Arakelyan A
Generation of three induced pluripotent stem cell lines (RAUi001-A, RAUi001-B and RAUi001-C) from peripheral blood mononuclear cells of a healthy Armenian individual
Grigor'eva EV et al. Generation of three induced pluripotent stem cell lines (RAUi001-A, RAUi001-B and RAUi001-C) from peripheral blood mononuclear cells of a healthy Armenian individual. . 2023-09-00. Pubmed ID: 37354743; DOI: 10.1016/j.scr.2023.103147 RAUi001-ARAUi001-BRAUi001-C 2023-09-00 2023-09-00 PubMed: 37354743 DOI: 10.1016/j.scr.2023.103147 -
Ovchinnikov DA, Jong S, Cuddy C, Scheffer IE, Maljevic S, Petrou S
Generation of an iPSC line (FINi001-A) from a girl with developmental and epileptic encephalopathy due to a heterozygous gain-of-function p.R1882Q variant in the voltage-gated sodium channel Na(v)1.2 protein encoded by the SCN2A gene
Ovchinnikov DA et al. Generation of an iPSC line (FINi001-A) from a girl with developmental and epileptic encephalopathy due to a heterozygous gain-of-function p.R1882Q variant in the voltage-gated sodium channel Na(v)1.2 protein encoded by the SCN2A gene. . 2023-09-00. Pubmed ID: 37597357; DOI: 10.1016/j.scr.2023.103179 FINi001-A 2023-09-00 2023-09-00 PubMed: 37597357 DOI: 10.1016/j.scr.2023.103179Associated cell lines:
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Jeong J, Lee D, Park BC, Lee TH, Park SW
Establishment of a TNFRSF11B knock-out human induced pluripotent stem cell line (KSCBi002-B-2) via CRISPR/Cas9 system
Jeong J et al. Establishment of a TNFRSF11B knock-out human induced pluripotent stem cell line (KSCBi002-B-2) via CRISPR/Cas9 system. . 2023-09-00. Pubmed ID: 37481965; DOI: 10.1016/j.scr.2023.103167 KSCBi002-BKSCBi002-B-2 2023-09-00 2023-09-00 PubMed: 37481965 DOI: 10.1016/j.scr.2023.103167Associated cell lines:
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Pugsley K, Namipashaki A, Vlahos K, Furley K, Graham A, Johnson BP, Kallady K, Kuah JY, Mohanakumar Sindhu VP, Suter A, Hawi Z, Bellgrove MA
Generation of induced pluripotent stem cell lines from three individuals with autism spectrum disorder
Pugsley K et al. Generation of induced pluripotent stem cell lines from three individuals with autism spectrum disorder. . 2023-09-00. Pubmed ID: 37494850; DOI: 10.1016/j.scr.2023.103170 MONUi001-AMONUi001-BMONUi001-CMONUi002-AMONUi002-BMONUi002-CMONUi003-AMONUi003-BMONUi003-C 2023-09-00 2023-09-00 PubMed: 37494850 DOI: 10.1016/j.scr.2023.103170Associated cell lines:
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Wilken MB, Maguire JA, Dungan LV, Gagne A, Osorio-Quintero C, Waxman EA, Chou ST, Gadue P, French DL, Thom CS
Generation of a human Tropomyosin 1 knockout iPSC line
Wilken MB et al. Generation of a human Tropomyosin 1 knockout iPSC line. . 2023-09-00. Pubmed ID: 37422949; DOI: 10.1016/j.scr.2023.103161; PMC: PMC10507314 SCSe001-ASCSe001-A-3CHOPi013-A 2023-09-00 2023-09-00 PubMed: 37422949 DOI: 10.1016/j.scr.2023.103161Associated cell lines:
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Hajduchova D, Suroviakova S, Mersakova S, Brany D, Zahumenska R, Rehak M, Skovierova H, Nováková S, Nosal V, Marcinek J, Kalman M, Jozef Pec M, Brozmanova M, Melegova J, Juhas S, Juhasova J, Studenovska H, Mitruskova B, Pokusa M, Samec M, Samos M, Nicodemou A, Danisovic L, Dankova Z, Kurca E, Lexova Kolejakova K, Chandoga J, Plank L, Halasova E, Pecova R, Strnadel J
Modelling Duchenne muscular dystrophy in vitro with newly generated, blood cell-derived induced pluripotent stem cell line ORIONi003-A
Hajduchova D et al. Modelling Duchenne muscular dystrophy in vitro with newly generated, blood cell-derived induced pluripotent stem cell line ORIONi003-A. . 2023-09-00. Pubmed ID: 37643496; DOI: 10.1016/j.scr.2023.103187 ORIONi003-A 2023-09-00 2023-09-00 PubMed: 37643496 DOI: 10.1016/j.scr.2023.103187Associated cell lines:
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Amin G, Castañeda SL, Zabalegui F, Belli C, Atorrasagasti C, Miriuka SG, Moro LN
Generation of two edited iPSCs lines by CRISPR/Cas9 with point mutations in PKP2 gene for arrhythmogenic cardiomyopathy in vitro modeling
Amin G et al. Generation of two edited iPSCs lines by CRISPR/Cas9 with point mutations in PKP2 gene for arrhythmogenic cardiomyopathy in vitro modeling. . 2023-09-00. Pubmed ID: 37393721; DOI: 10.1016/j.scr.2023.103157 INEUi002-A-1INEUi002-A-2 2023-09-00 2023-09-00 PubMed: 37393721 DOI: 10.1016/j.scr.2023.103157Associated cell lines:
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Piechota M, Latoszek E, Liszewska E, Hansíková H, Klempíř J, Mühlbäck A, Landwehrmeyer GB, Kuźnicki J, Czeredys M
Generation of two human iPSC lines from dermal fibroblasts of adult- and juvenile-onset Huntington's disease patients and two healthy donors
Piechota M et al. Generation of two human iPSC lines from dermal fibroblasts of adult- and juvenile-onset Huntington's disease patients and two healthy donors. . 2023-09-00. Pubmed ID: 37651831; DOI: 10.1016/j.scr.2023.103194 IIMCBi001-AIIMCBi002-AIIMCBi007-AIIMCBi008-AIIMCBi003-BIIMCBi006-B 2023-09-00 2023-09-00 PubMed: 37651831 DOI: 10.1016/j.scr.2023.103194Associated cell lines:
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Hashmi SK, Schneider S, Gagne AL, Maguire JA, Anderson S, Gadue P, Heuckeroth RO, French DL
Generation of CHOPe003-A ESC line to study an ACTG2 variant affecting smooth muscle development and function
Hashmi SK et al. Generation of CHOPe003-A ESC line to study an ACTG2 variant affecting smooth muscle development and function. . 2023-09-00. Pubmed ID: 37643495; DOI: 10.1016/j.scr.2023.103186; PMC: PMC10509821 CHOPi002-ACHOPi003-ACHOPe003-A 2023-09-00 2023-09-00 PubMed: 37643495 DOI: 10.1016/j.scr.2023.103186Associated cell lines:
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Cattelan G, Sophie Frommelt L, Volani C, Colliva A, Ciucci G, Paldino A, Dal Ferro M, Di Segni M, Silipigni R, Pramstaller PP, De Bortoli M, Zacchigna S, Rossini A
Generation of human induced pluripotent stem cell line EURACi015-A from a patient affected by dilated cardiomyopathy carrying the Lamin A/C p.Glu161Lys mutation
Cattelan G et al. Generation of human induced pluripotent stem cell line EURACi015-A from a patient affected by dilated cardiomyopathy carrying the Lamin A/C p.Glu161Lys mutation. . 2023-09-00. Pubmed ID: 37535990; DOI: 10.1016/j.scr.2023.103172 CMDi001-ACMDi002-AEURACi015-A 2023-09-00 2023-09-00 PubMed: 37535990 DOI: 10.1016/j.scr.2023.103172Associated cell lines:
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Belova L, Demchenko A, Kochergin-Nikitsky K, Kondrateva E, Slesarenko Y, Salikhova D, Lavrov A, Efremova A, Bukharova T, Goldshtein D, Smirnikhina S
Recombinant Adeno-associated Viral Vectors Serotypes 6 and 9 are Able to Transduce Human Tracheal Epithelial Cells but Not Human Induced Pluripotent Stem Cells
Belova L et al. Recombinant Adeno-associated Viral Vectors Serotypes 6 and 9 are Able to Transduce Human Tracheal Epithelial Cells but Not Human Induced Pluripotent Stem Cells. . 2023-09-00. Pubmed ID: 36707468; DOI: 10.1007/s12033-023-00668-4 RCMGi001-A 2023-09-00 2023-09-00 PubMed: 36707468 DOI: 10.1007/s12033-023-00668-4Associated cell lines:
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Ansori Arif NM., Antonius Yulanda, Susilo Raden JK., Hayaza Suhaila, Kharisma Viol D., Parikesit Arli A., Zainul Rahadian, Jakhmola Vikash, Saklani Taru, Rebezov Maksim, Ullah Md. Emdad, Maksimiuk Nikolai, Derkho Marina, Burkov Pavel
Application of CRISPR-Cas9 genome editing technology in various fields: A review
Ansori Arif NM. et al. Application of CRISPR-Cas9 genome editing technology in various fields: A review. . 2023-08-31. DOI: 10.52225/narra.v3i2.184 IRFMNi003-AIRFMNi003-A-1IRFMNi003-A-2 2023-08-31 2023-08-31 DOI: 10.52225/narra.v3i2.184Associated cell lines:
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Ncube A, Bewersdorf L, Spitzhorn LS, Loerch C, Bohndorf M, Graffmann N, May L, Amzou S, Fromme M, Wruck W, Strnad P, Adjaye J
Generation of two Alpha-I antitrypsin deficiency patient-derived induced pluripotent stem cell lines ISRM-AATD-iPSC-1 (HHUUKDi011-A) and ISRM-AATD-iPSC-2 (HHUUKDi012-A)
Ncube A et al. Generation of two Alpha-I antitrypsin deficiency patient-derived induced pluripotent stem cell lines ISRM-AATD-iPSC-1 (HHUUKDi011-A) and ISRM-AATD-iPSC-2 (HHUUKDi012-A). . 2023-09-00. Pubmed ID: 37506509; DOI: 10.1016/j.scr.2023.103171 HHUUKDi011-AHHUUKDi012-A 2023-09-00 2023-09-00 PubMed: 37506509 DOI: 10.1016/j.scr.2023.103171Associated cell lines:
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Davidson Jennilee M., Wu Sharlynn S. L., Rayner Stephanie L., Cheng Flora, Duncan Kimberley, Russo Carlo, Newbery Michelle, Ding Kunjie, Scherer Natalie M., Balez Rachelle, García-Redondo Alberto, Rábano Alberto, Rosa-Fernandes Livia, Ooi Lezanne, Williams Kelly L., Morsch Marco, Blair Ian P., Di Ieva Antonio, Yang Shu, Chung Roger S., Lee Albert
The E3 Ubiquitin Ligase SCF Cyclin F Promotes Sequestosome-1/p62 Insolubility and Foci Formation and is Dysregulated in ALS and FTD Pathogenesis
Davidson Jennilee M. et al. The E3 Ubiquitin Ligase SCF Cyclin F Promotes Sequestosome-1/p62 Insolubility and Foci Formation and is Dysregulated in ALS and FTD Pathogenesis. . 2023-09-00. DOI: 10.1007/s12035-023-03355-2 UOWi005-A 2023-09-00 2023-09-00 DOI: 10.1007/s12035-023-03355-2Associated cell lines:
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Boissart C, Chatrousse L, Poullion T, El-Kassar L, Giraud-Triboult K, Benchoua A
CRISPR/Cas9-mediated generation of human embryonic stem cell sub-lines with HPRT1 gene knockout to model Lesch Nyhan disease
Boissart C et al. CRISPR/Cas9-mediated generation of human embryonic stem cell sub-lines with HPRT1 gene knockout to model Lesch Nyhan disease. . 2023-09-00. Pubmed ID: 37331109; DOI: 10.1016/j.scr.2023.103144 CEBe033-A-8CEBe033-A-9CEBe033-A-10CEBe033-A-11 2023-09-00 2023-09-00 PubMed: 37331109 DOI: 10.1016/j.scr.2023.103144Associated cell lines:
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Li B, Zhou Y, Che F, Zhou R, Mo L, Zhang L, Wang G, Yang Y
Establishment of a novel human induced pluripotent stem cell line (SIPDi001-A) with compound heterozygous mutations in the UBR7 gene from a Li-Campeau syndrome patient
Li B et al. Establishment of a novel human induced pluripotent stem cell line (SIPDi001-A) with compound heterozygous mutations in the UBR7 gene from a Li-Campeau syndrome patient. . 2023-09-00. Pubmed ID: 37478672; DOI: 10.1016/j.scr.2023.103165 XACHi005-AXACHi006-ASIPDi001-A 2023-09-00 2023-09-00 PubMed: 37478672 DOI: 10.1016/j.scr.2023.103165Associated cell lines:
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Gao J, Cao C, Shi M, Hong S, Guo S, Li J, Liang T, Song P, Xu R, Li N
Kaempferol inhibits SARS-CoV-2 invasion by impairing heptad repeats-mediated viral fusion
Gao J et al. Kaempferol inhibits SARS-CoV-2 invasion by impairing heptad repeats-mediated viral fusion. . 2023-09-00. Pubmed ID: 37421767; DOI: 10.1016/j.phymed.2023.154942; PMC: PMC10289257 IBTCMi002-A 2023-09-00 2023-09-00 PubMed: 37421767 DOI: 10.1016/j.phymed.2023.154942Associated cell lines:
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Fang X, Kim JH, Cui S, Shin YJ, Lee H, Ko EJ, Cheong HI, Kim S, Kim HS, Kim M, Yang CW, Lim SW, Chung BH
Generation of a human induced pluripotent stem cell line from a patient with dent disease
Fang X et al. Generation of a human induced pluripotent stem cell line from a patient with dent disease. . 2023-09-00. Pubmed ID: 37356184; DOI: 10.1016/j.scr.2023.103140 CMCi011-A 2023-09-00 2023-09-00 PubMed: 37356184 DOI: 10.1016/j.scr.2023.103140Associated cell lines:
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Wang T, Zhu K, Yu W, Peng L, Wang H, Wu Q
Generation of an iPSC line (TSHSUi001-A) from a patient with Peutz-Jeghers syndrome due to STK11 mutation
Wang T et al. Generation of an iPSC line (TSHSUi001-A) from a patient with Peutz-Jeghers syndrome due to STK11 mutation. . 2023-09-00. Pubmed ID: 37392704; DOI: 10.1016/j.scr.2023.103152 TSHSUi001-A 2023-09-00 2023-09-00 PubMed: 37392704 DOI: 10.1016/j.scr.2023.103152Associated cell lines:
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Chahine M, Jauvin D, Pierre M, Puymirat J, Boutjdir M
Lymphoblastoid cell lines derived from iPSCs of a myotonic dystrophy type 1 patient carrying 700 CTG repeats (CBRCULi007-A) and a control (CBRCULi006-A)
Chahine M et al. Lymphoblastoid cell lines derived from iPSCs of a myotonic dystrophy type 1 patient carrying 700 CTG repeats (CBRCULi007-A) and a control (CBRCULi006-A). . 2023-09-00. Pubmed ID: 37352653; DOI: 10.1016/j.scr.2023.103148 CBRCULi001-ACBRCULi002-ACBRCULi003-ACBRCULi004-ACBRCULi005-ACBRCULi006-ACBRCULi007-A 2023-09-00 2023-09-00 PubMed: 37352653 DOI: 10.1016/j.scr.2023.103148Associated cell lines:
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Ozgoren OK, Sequiera GL, Ferrari Bardile C, Gjervan SC, Salman A, Lehman A, Turvey SE, Ross CJD, Stockler S, Pouladi MA
Generation of a human induced pluripotent stem cell line from a patient with hypomyelinating leukodystrophy 22 (HLD22)
Ozgoren OK et al. Generation of a human induced pluripotent stem cell line from a patient with hypomyelinating leukodystrophy 22 (HLD22). . 2023-09-00. Pubmed ID: 37531724; DOI: 10.1016/j.scr.2023.103174 UBCi002-A 2023-09-00 2023-09-00 PubMed: 37531724 DOI: 10.1016/j.scr.2023.103174Associated cell lines:
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Nahon DM, Ganesh S, van den Hil FE, Freund C, Mummery CL, Orlova VV
Genetic repair of a human induced pluripotent cell line from patient with Dutch-type cerebral amyloid angiopathy
Nahon DM et al. Genetic repair of a human induced pluripotent cell line from patient with Dutch-type cerebral amyloid angiopathy. . 2023-09-00. Pubmed ID: 37603921; DOI: 10.1016/j.scr.2023.103180 LUMCi005-ALUMCi005-A-3LUMCi005-A-4 2023-09-00 2023-09-00 PubMed: 37603921 DOI: 10.1016/j.scr.2023.103180Associated cell lines:
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Sun W, Wang P, Gong J, Chen Y, Yang Y, Luan H, Li S, Li R, Wei C
Generation of induced pluripotent stem cell line (XWHNi002-A) from a female with APP gene mutation
Sun W et al. Generation of induced pluripotent stem cell line (XWHNi002-A) from a female with APP gene mutation. . 2023-09-00. Pubmed ID: 37356183; DOI: 10.1016/j.scr.2023.103149 XWHNi002-A 2023-09-00 2023-09-00 PubMed: 37356183 DOI: 10.1016/j.scr.2023.103149Associated cell lines:
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Hayal Taha Bartu, Doğan Ayşegül, Şenkal Selinay, Bulut Ezgi, Şişli Hatice Burcu, Şahin Fikrettin
Evaluation of the effect of boron derivatives on cardiac differentiation of mouse pluripotent stem cells
Hayal Taha Bartu et al. Evaluation of the effect of boron derivatives on cardiac differentiation of mouse pluripotent stem cells. . 2023-09-00. DOI: 10.1016/j.jtemb.2023.127258 SJTUXHi002-A 2023-09-00 2023-09-00 DOI: 10.1016/j.jtemb.2023.127258Associated cell lines:
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Chapotte-Baldacci CA, Jauvin D, Chahine M
Generation of control iPSC lines CBRCULi008-A and CBRCULi009-A derived from lymphoblastoid cell lines
Chapotte-Baldacci CA et al. Generation of control iPSC lines CBRCULi008-A and CBRCULi009-A derived from lymphoblastoid cell lines. . 2023-09-00. Pubmed ID: 37473461; DOI: 10.1016/j.scr.2023.103168 CHUQi001-ACBRCULi008-ACBRCULi009-A 2023-09-00 2023-09-00 PubMed: 37473461 DOI: 10.1016/j.scr.2023.103168Associated cell lines:
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Wilson Carey, Gattuso James J., Hannan Anthony J., Renoir Thibault
Mechanisms of pathogenesis and environmental moderators in preclinical models of compulsive-like behaviours
Wilson Carey et al. Mechanisms of pathogenesis and environmental moderators in preclinical models of compulsive-like behaviours. . 2023-09-00. DOI: 10.1016/j.nbd.2023.106223 TUSMi004-A 2023-09-00 2023-09-00 DOI: 10.1016/j.nbd.2023.106223Associated cell lines:
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Li S, Fraser S, Ranpura G, Lim S, Singer ES, Parker JDK, Crowe J, Bagnall RD, Laksman Z, Semsarian C
Generation of an induced pluripotent stem cell line from a patient with conduction disease and recurrent ventricular fibrillation with a sodium voltage-gated channel alpha subunit 5 (SCN5A) gene c.392 + 3A > G splice-site variant
Li S et al. Generation of an induced pluripotent stem cell line from a patient with conduction disease and recurrent ventricular fibrillation with a sodium voltage-gated channel alpha subunit 5 (SCN5A) gene c.392 + 3A > G splice-site variant. . 2023-09-00. Pubmed ID: 37385135; DOI: 10.1016/j.scr.2023.103153 CIAUi002-C 2023-09-00 2023-09-00 PubMed: 37385135 DOI: 10.1016/j.scr.2023.103153Associated cell lines:
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Dai Yuwei, Wu Ziqiong, Chen Yitong, Ye Xinjian, Wang Chaowei, Zhu Huiyong
OCT4’s role and mechanism underlying oral squamous cell carcinoma
Dai Yuwei et al. OCT4’s role and mechanism underlying oral squamous cell carcinoma. . 2023-09-00. DOI: 10.1631/jzus.b2200602 JTUi005-A 2023-09-00 2023-09-00 DOI: 10.1631/jzus.b2200602Associated cell lines:
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Chen W, Wang Y, Shen L, Huang S, Yang X, Wu D
Human induced pluripotent stem cells derived from a patient with a mutation of SERPINC1 c.236G>A (p.R79H)
Chen W et al. Human induced pluripotent stem cells derived from a patient with a mutation of SERPINC1 c.236G>A (p.R79H). . 2023-09-00. Pubmed ID: 37385134; DOI: 10.1016/j.scr.2023.103150 ZZUNEUi014-ASFPHi001-A 2023-09-00 2023-09-00 PubMed: 37385134 DOI: 10.1016/j.scr.2023.103150Associated cell lines:
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Kobayashi GS, Vieira-Silva GA, Varella-Branco E, Moreira DP, Kitajima JPFW, Hemza CRML, Mingroni-Netto RC, Lojudice FH, Oiticica J, Bento RF, Batissoco AC, Lezirovitz K
Generation of four induced pluripotent stem cells lines from PBMC of the DFNA58 family members: Two hearing-impaired duplication carriers (USPi006-A e USPi007-A) and two normal-hearing noncarriers (USPi004-A and USPi005-A)
Kobayashi GS et al. Generation of four induced pluripotent stem cells lines from PBMC of the DFNA58 family members: Two hearing-impaired duplication carriers (USPi006-A e USPi007-A) and two normal-hearing noncarriers (USPi004-A and USPi005-A). . 2023-09-00. Pubmed ID: 37595341; DOI: 10.1016/j.scr.2023.103181 USPi004-AUSPi005-AUSPi006-AUSPi007-A 2023-09-00 2023-09-00 PubMed: 37595341 DOI: 10.1016/j.scr.2023.103181 -
Cerrada Victoria, García-Consuegra Inés, Arenas Joaquín, Gallardo M. Esther
Creation of an iPSC-Based Skeletal Muscle Model of McArdle Disease Harbouring the Mutation c.2392T>C (p.Trp798Arg) in the PYGM Gene
Cerrada Victoria et al. Creation of an iPSC-Based Skeletal Muscle Model of McArdle Disease Harbouring the Mutation c.2392T>C (p.Trp798Arg) in the PYGM Gene. . 2023-08-31. DOI: 10.3390/biomedicines11092434 IISHDOi007-A 2023-08-31 2023-08-31 DOI: 10.3390/biomedicines11092434Associated cell lines:
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Chemla A, Arena G, Onal G, Walter J, Berenguer-Escuder C, Grossmann D, Grünewald A, Schwamborn JC, Krüger R
Generation of two induced pluripotent stem cell lines and the corresponding isogenic controls from Parkinson's disease patients carrying the heterozygous mutations c.815G > A (p.R272Q) or c.1348C > T (p.R450C) in the RHOT1 gene encoding Miro1
Chemla A et al. Generation of two induced pluripotent stem cell lines and the corresponding isogenic controls from Parkinson's disease patients carrying the heterozygous mutations c.815G > A (p.R272Q) or c.1348C > T (p.R450C) in the RHOT1 gene encoding Miro1. . 2023-09-00. Pubmed ID: 37364399; DOI: 10.1016/j.scr.2023.103145 LCSBi009-ALCSBi009-A-1LCSBi010-ALCSBi010-A-1LCSBi010-A-2 2023-09-00 2023-09-00 PubMed: 37364399 DOI: 10.1016/j.scr.2023.103145Associated cell lines:
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Xi Y, Zhang H, Yang X, Ai D, Liu Y, Song W
Establishment of induced pluripotent stem cell line SDPHi003-A from a healthy male donor
Xi Y et al. Establishment of induced pluripotent stem cell line SDPHi003-A from a healthy male donor. . 2023-09-00. Pubmed ID: 37429069; DOI: 10.1016/j.scr.2023.103160 SDPHi003-A 2023-09-00 2023-09-00 PubMed: 37429069 DOI: 10.1016/j.scr.2023.103160Associated cell lines:
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Batool L, Storozhuk O, Raab C, Madlen Beez C, Selig M, Harder A, Kurtz A
Generation of two human induced pluripotent stem cell lines from a patient with Neurofibromatosis type 1 (NF1) and pathogenic NF1 gene variant c.1466 A>G BCRTi011-A as well as a first-degree healthy relative (BCRTi010-A)
Batool L et al. Generation of two human induced pluripotent stem cell lines from a patient with Neurofibromatosis type 1 (NF1) and pathogenic NF1 gene variant c.1466 A>G BCRTi011-A as well as a first-degree healthy relative (BCRTi010-A). . 2023-09-00. Pubmed ID: 37619442; DOI: 10.1016/j.scr.2023.103184 BCRTi010-ABCRTi011-A 2023-09-00 2023-09-00 PubMed: 37619442 DOI: 10.1016/j.scr.2023.103184Associated cell lines:
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Raina K, Joshi G, Modak K, Premkumar C, Priyanka S, Rajesh P, Velayudhan SR, Thummer RP
Generation and characterization of induced pluripotent stem cell line IITGi001-A derived from adult human primary dermal fibroblasts
Raina K et al. Generation and characterization of induced pluripotent stem cell line IITGi001-A derived from adult human primary dermal fibroblasts. . 2023-09-00. Pubmed ID: 37392703; DOI: 10.1016/j.scr.2023.103159 CSCRi005-AIITGi001-A 2023-09-00 2023-09-00 PubMed: 37392703 DOI: 10.1016/j.scr.2023.103159Associated cell lines:
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Alonzo M, Ye S, Beckman B, Texter K, Garg V, Zhao MT
Creation of iPSC line NCHi004-A from a patient with down syndrome and congenital heart defects
Alonzo M et al. Creation of iPSC line NCHi004-A from a patient with down syndrome and congenital heart defects. . 2023-09-00. Pubmed ID: 37393719; DOI: 10.1016/j.scr.2023.103156; PMC: PMC10578300 NCHi004-A 2023-09-00 2023-09-00 PubMed: 37393719 DOI: 10.1016/j.scr.2023.103156Associated cell lines:
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Raj Aishwarya, Banerjee Roon, Santhoshkumar Rashmi, Sagar Chandrasekhar, Datta Indrani
Presence of Extracellular Alpha-Synuclein Aggregates Trigger Astrocytic Degeneration Through Enhanced Membrane Rigidity and Deregulation of Store-Operated Calcium Entry (SOCE) into the Endoplasmic Reticulum
Raj Aishwarya et al. Presence of Extracellular Alpha-Synuclein Aggregates Trigger Astrocytic Degeneration Through Enhanced Membrane Rigidity and Deregulation of Store-Operated Calcium Entry (SOCE) into the Endoplasmic Reticulum. . 2023-09-00. DOI: 10.1007/s12035-023-03400-0 NIMHi001-ANIMHi004-ANIMHi005-ANIMHi006-A 2023-09-00 2023-09-00 DOI: 10.1007/s12035-023-03400-0Associated cell lines:
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Wang Y, Yang X, Zhang H, Liu N, Liu Y, Gai Z, Liu Y, Lv Y
Generation of a transgene-free iPS cell line (SDQLCHi053-A) from a young girl carrying a heterozygous mutation (c.427C > T) in SYNGAP1 gene
Wang Y et al. Generation of a transgene-free iPS cell line (SDQLCHi053-A) from a young girl carrying a heterozygous mutation (c.427C > T) in SYNGAP1 gene. . 2023-09-00. Pubmed ID: 37385133; DOI: 10.1016/j.scr.2023.103132 SDQLCHi053-A 2023-09-00 2023-09-00 PubMed: 37385133 DOI: 10.1016/j.scr.2023.103132Associated cell lines:
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Karjosukarso DW, Bukkems F, Duijkers L, Leijsten N, Collin RWJ
Generation of three isogenic control lines from patient-derived iPSCs carrying bi-allelic ABCA4 variants underlying Stargardt disease
Karjosukarso DW et al. Generation of three isogenic control lines from patient-derived iPSCs carrying bi-allelic ABCA4 variants underlying Stargardt disease. . 2023-09-00. Pubmed ID: 37480818; DOI: 10.1016/j.scr.2023.103169 RMCGENi005-ASCTCi017-A-1SCTCi018-A-1RMCGENi005-A-1 2023-09-00 2023-09-00 PubMed: 37480818 DOI: 10.1016/j.scr.2023.103169Associated cell lines:
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Efendic F, Krohn S, Murua Escobar H, Venkateswaran S, Bennett SAL, Hermann A, Frech MJ
Generation of the human iPSC lines AKOSi011-A carrying the mutation p.Pro65Ser/p.Asp35T and AKOSi012-A, carrying the mutation p.Tyr231His, derived from FAHN patient fibroblasts
Efendic F et al. Generation of the human iPSC lines AKOSi011-A carrying the mutation p.Pro65Ser/p.Asp35T and AKOSi012-A, carrying the mutation p.Tyr231His, derived from FAHN patient fibroblasts. . 2023-09-00. Pubmed ID: 37573804; DOI: 10.1016/j.scr.2023.103178 AKOSi010-AAKOSi011-AAKOSi012-A 2023-09-00 2023-09-00 PubMed: 37573804 DOI: 10.1016/j.scr.2023.103178Associated cell lines:
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Rivera-Sánchez P, Søndergaard L, Wathikthinnakon M, B D Magnusson H, Frederiksen HR, Aabæk Hammer F, Taleb R, Christian Cassidy C, Tranholm Bruun M, Tümer Z, Holst B, Brasch-Andersen C, Møller RS, Freude K, Chandrasekaran A
Generation of eight hiPSCs lines from two pathogenic variants in CACNA1A using the CRISPR-Cas9 gene editing technology
Rivera-Sánchez P et al. Generation of eight hiPSCs lines from two pathogenic variants in CACNA1A using the CRISPR-Cas9 gene editing technology. . 2023-09-00. Pubmed ID: 37651830; DOI: 10.1016/j.scr.2023.103193 BIONi010-C-56BIONi010-C-57BIONi010-C-58BIONi010-C-59BIONi010-C-60BIONi010-C-61BIONi010-C-62BIONi010-C-63 2023-09-00 2023-09-00 PubMed: 37651830 DOI: 10.1016/j.scr.2023.103193Associated cell lines:
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Jonsgaard Larsen L, Birk Møller L
Generation of induced pluripotent stem cells, KCi004-A derived from a male with Parkinson's disease and homozygous for the PINK1 variant c.1366C > T, p.Gln456
Jonsgaard Larsen L et al. Generation of induced pluripotent stem cells, KCi004-A derived from a male with Parkinson's disease and homozygous for the PINK1 variant c.1366C > T, p.Gln456. . 2023-09-00. Pubmed ID: 37524028; DOI: 10.1016/j.scr.2023.103175 KCi004-A 2023-09-00 2023-09-00 PubMed: 37524028 DOI: 10.1016/j.scr.2023.103175Associated cell lines:
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Heseding H, Jahn K, Brändl B, Haase A, Shum IO, Kohrn T, Bleich S, Frieling H, Martin U, Müller FJ, Wunderlich S, Deest M
Generation of an induced pluripotent stem cell line, ZIPi021-A, from fibroblasts of a Prader-Willi syndrome patient with maternal uniparental disomy (mUPD)
Heseding H et al. Generation of an induced pluripotent stem cell line, ZIPi021-A, from fibroblasts of a Prader-Willi syndrome patient with maternal uniparental disomy (mUPD). . 2023-09-00. Pubmed ID: 37343429; DOI: 10.1016/j.scr.2023.103143 ZIPi021-A 2023-09-00 2023-09-00 PubMed: 37343429 DOI: 10.1016/j.scr.2023.103143Associated cell lines:
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Montero-Calle P, Flandes-Iparraguirre M, Kuebler B, Arán B, Larequi E, Anaut I, Coppiello G, Aranguren XL, Veiga A, Elorz MTB, de Yébenes MG, Gavira JJ, Prósper F, Iglesias-García O, Vega MMM
Generation of an induced pluripotent stem cell line (ESi107-A) from a transthyretin amyloid cardiomyopathy (ATTR-CM) patient carrying a p.Ser43Asn mutation in the TTR gene
Montero-Calle P et al. Generation of an induced pluripotent stem cell line (ESi107-A) from a transthyretin amyloid cardiomyopathy (ATTR-CM) patient carrying a p.Ser43Asn mutation in the TTR gene. . 2023-09-00. Pubmed ID: 37660554; DOI: 10.1016/j.scr.2023.103189 ESi107-A 2023-09-00 2023-09-00 PubMed: 37660554 DOI: 10.1016/j.scr.2023.103189Associated cell lines:
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Yang Meimei, Liu Min, Sánchez Yajaira Feller, Avazzadeh Sahar, Quinlan Leo R., Liu Gang, Lu Yin, Yang Guangming, O'Brien Timothy, Henshall David C., Hardiman Orla, Shen Sanbing
A novel protocol to derive cervical motor neurons from induced pluripotent stem cells for amyotrophic lateral sclerosis
Yang Meimei et al. A novel protocol to derive cervical motor neurons from induced pluripotent stem cells for amyotrophic lateral sclerosis. . 2023-09-00. DOI: 10.1016/j.stemcr.2023.07.004 NUIGi033-ANUIGi034-ANUIGi038-ANUIGi038-BNUIGi043-ANUIGi043-BNUIGi043-CNUIGi044-ANUIGi044-BNUIGi044-C 2023-09-00 2023-09-00 DOI: 10.1016/j.stemcr.2023.07.004Associated cell lines:
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Karjosukarso DW, Bukkems F, Duijkers L, Leijsten N, Hoyng CB, Collin RWJ
Generation of iPSC lines from three Stargardt patients carrying bi-allelic ABCA4 variants
Karjosukarso DW et al. Generation of iPSC lines from three Stargardt patients carrying bi-allelic ABCA4 variants. . 2023-09-00. Pubmed ID: 37441824; DOI: 10.1016/j.scr.2023.103164 SCTCi017-ASCTCi018-ARMCGENi005-A 2023-09-00 2023-09-00 PubMed: 37441824 DOI: 10.1016/j.scr.2023.103164Associated cell lines:
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Zhu K, Zhao J, Qin F, Chen X, Xu H, Li X, Tao H
An integration-free iPSC line ZZUNEUi029-A derived from peripheral blood mononuclear cells of a patient with familial hypercholesterolemia carrying a mutation in LDLR gene
Zhu K et al. An integration-free iPSC line ZZUNEUi029-A derived from peripheral blood mononuclear cells of a patient with familial hypercholesterolemia carrying a mutation in LDLR gene. . 2023-09-00. Pubmed ID: 37586167; DOI: 10.1016/j.scr.2023.103182 ZZUNEUi029-A 2023-09-00 2023-09-00 PubMed: 37586167 DOI: 10.1016/j.scr.2023.103182Associated cell lines:
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Hashmi SK, Schneider S, Gagne AL, Maguire JA, Gadue P, Heuckeroth RO, French DL
Generation of CHOPi012-A iPSC line from a patient with visceral myopathy-related chronic intestinal pseudo-obstruction
Hashmi SK et al. Generation of CHOPi012-A iPSC line from a patient with visceral myopathy-related chronic intestinal pseudo-obstruction. . 2023-09-00. Pubmed ID: 37572398; DOI: 10.1016/j.scr.2023.103176; PMC: PMC11299795 CHOPi002-ACHOPi003-ACHOPi012-A 2023-09-00 2023-09-00 PubMed: 37572398 DOI: 10.1016/j.scr.2023.103176Associated cell lines:
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Wan Z, Guan J, Li Y, Zhang H, Wang B, Yang X, Jin X, Ma X, Liu Y
Generation and characterization of a human induced pluripotent stem cell line (SDQLCHi052-A) from peripheral blood mononuclear cells derived from a healthy Chinese donor
Wan Z et al. Generation and characterization of a human induced pluripotent stem cell line (SDQLCHi052-A) from peripheral blood mononuclear cells derived from a healthy Chinese donor. . 2023-09-00. Pubmed ID: 37320988; DOI: 10.1016/j.scr.2023.103139 SDQLCHi045-ASDQLCHi052-A 2023-09-00 2023-09-00 PubMed: 37320988 DOI: 10.1016/j.scr.2023.103139Associated cell lines:
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Pietsch N, Cheng J, Fazio A, Ewald L, Alizoti E, Krämer E, Orthey E, Carrier L, Singh SR
Generation of a homozygous CRYAB p.Arg120Gly mutant (UKEi001-A-1) from a human iPSC line
Pietsch N et al. Generation of a homozygous CRYAB p.Arg120Gly mutant (UKEi001-A-1) from a human iPSC line. . 2023-09-00. Pubmed ID: 37633027; DOI: 10.1016/j.scr.2023.103188 UKEi001-AUKEi001-A-1 2023-09-00 2023-09-00 PubMed: 37633027 DOI: 10.1016/j.scr.2023.103188Associated cell lines:
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Schuurmans IME, Wu KM, van Karnebeek CDM, Nadif Kasri N, Garanto A
Generation of an induced pluripotent stem cell line carrying biallelic deletions (SCTCi019-B) in ALDH7A1 using CRISPR/Cas9
Schuurmans IME et al. Generation of an induced pluripotent stem cell line carrying biallelic deletions (SCTCi019-B) in ALDH7A1 using CRISPR/Cas9. . 2023-09-00. Pubmed ID: 37540965; DOI: 10.1016/j.scr.2023.103173 SCTCi019-B 2023-09-00 2023-09-00 PubMed: 37540965 DOI: 10.1016/j.scr.2023.103173Associated cell lines:
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Ortiz-Vitali Jose L., Wu Jianbo, Xu Nasa, Shieh Annie W., Niknejad Nima, Takeuchi Megumi, Paradas Carmen, Lin Chunru, Jafar-Nejad Hamed, Haltiwanger Robert S., Wang Sidney H., Darabi Radbod
Disease modeling and gene correction of LGMDR21 iPSCs elucidates the role of POGLUT1 in skeletal muscle maintenance, regeneration, and the satellite cell niche
Ortiz-Vitali Jose L. et al. Disease modeling and gene correction of LGMDR21 iPSCs elucidates the role of POGLUT1 in skeletal muscle maintenance, regeneration, and the satellite cell niche. . 2023-09-00. DOI: 10.1016/j.omtn.2023.07.037 CSCRMi001-A 2023-09-00 2023-09-00 DOI: 10.1016/j.omtn.2023.07.037Associated cell lines:
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Panchuk IO, Grigorieva OV, Kondrateva EV, Kurshakova EV, Tabakov V, Bychkov IO, Zakharova E, Orlova MD, Voronina ES, Pozhitnova VO, Lavrov AV, Smirnikhina SA, Kutsev SI
Generation of two iPSC lines from patient with Mucopolysaccharidosis IV B type and autosomal recessive non-syndromic hearing loss 12
Panchuk IO et al. Generation of two iPSC lines from patient with Mucopolysaccharidosis IV B type and autosomal recessive non-syndromic hearing loss 12. . 2023-09-00. Pubmed ID: 37643494; DOI: 10.1016/j.scr.2023.103183 RCMGi011-ARCMGi011-B 2023-09-00 2023-09-00 PubMed: 37643494 DOI: 10.1016/j.scr.2023.103183Associated cell lines:
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Jiang M, Tang C, Luo X, Zhou X, Chen M, Chi Y, Lai L, Zou Q
Generation of a homozygous RANGRF knockout hiPSC line by CRISPR/Cas9 system
Jiang M et al. Generation of a homozygous RANGRF knockout hiPSC line by CRISPR/Cas9 system. . 2023-09-00. Pubmed ID: 37327621; DOI: 10.1016/j.scr.2023.103136 WYUi002-A 2023-09-00 2023-09-00 PubMed: 37327621 DOI: 10.1016/j.scr.2023.103136Associated cell lines:
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Stewart R, Gadoud C, Krawczyk J, McInerney V, O'Brien T, Shen S, Allen NM
Generation of three induced pluripotent stem cell lines from a patient with KCNQ2 developmental and epileptic encephalopathy as a result of the pathogenic variant c.881C > T; p.Ala294Val (NUIGi059-A, NUIGi059-B, NUIGi059-C) and 3 healthy controls (NUIGi060-A, NUIGi060-B, NUIGi060-C)
Stewart R et al. Generation of three induced pluripotent stem cell lines from a patient with KCNQ2 developmental and epileptic encephalopathy as a result of the pathogenic variant c.881C > T; p.Ala294Val (NUIGi059-A, NUIGi059-B, NUIGi059-C) and 3 healthy controls (NUIGi060-A, NUIGi060-B, NUIGi060-C). . 2023-09-00. Pubmed ID: 37659345; DOI: 10.1016/j.scr.2023.103191 NUIGi059-ANUIGi059-BNUIGi059-CNUIGi060-ANUIGi060-BNUIGi060-C 2023-09-00 2023-09-00 PubMed: 37659345 DOI: 10.1016/j.scr.2023.103191Associated cell lines:
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Cunningham D, Stanberry I, Ye S, Alonzo M, Zhao MT, Garg V, Lilly B
Generation of iPSC line NCHi012-A from a patient with Alagille syndrome and heterozygous pathogenic variant in the JAG1 gene
Cunningham D et al. Generation of iPSC line NCHi012-A from a patient with Alagille syndrome and heterozygous pathogenic variant in the JAG1 gene. . 2023-09-00. Pubmed ID: 37549562; DOI: 10.1016/j.scr.2023.103177; PMC: PMC10528323 NCHi012-A 2023-09-00 2023-09-00 PubMed: 37549562 DOI: 10.1016/j.scr.2023.103177Associated cell lines:
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Owusu-Ansah K, Pavlinov I, Xu M, Beers J, Chen C, Zheng W, Zou J
Three induced pluripotent stem cell lines (TRNDi033-A, TRNDi034-A, TRNDi035-A) generated from lymphoblasts of three apparently healthy individuals
Owusu-Ansah K et al. Three induced pluripotent stem cell lines (TRNDi033-A, TRNDi034-A, TRNDi035-A) generated from lymphoblasts of three apparently healthy individuals. . 2023-09-00. Pubmed ID: 37393720; DOI: 10.1016/j.scr.2023.103135; PMC: PMC10529852 TRNDi033-ATRNDi034-ATRNDi035-A 2023-09-00 2023-09-00 PubMed: 37393720 DOI: 10.1016/j.scr.2023.103135Associated cell lines:
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Ghafouri-Fard Soudeh, Pourtavakoli Ashkan, Hussen Bashdar Mahmud, Taheri Mohammad, Ayatollahi Seyed Abdulmajid
A Review on the Role of Genetic Mutations in the Autism Spectrum Disorder
Ghafouri-Fard Soudeh et al. A Review on the Role of Genetic Mutations in the Autism Spectrum Disorder. . 2023-09-00. DOI: 10.1007/s12035-023-03405-9 SJTUXHi002-A 2023-09-00 2023-09-00 DOI: 10.1007/s12035-023-03405-9Associated cell lines:
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Siebert AL, Schwartz GB, Kubo H, Laronda MM
Induced pluripotent stem cell line generated from a patient with differences in sex development (DSD) and multiple genetic variants including a large deletion in NR5A1
Siebert AL et al. Induced pluripotent stem cell line generated from a patient with differences in sex development (DSD) and multiple genetic variants including a large deletion in NR5A1. . 2023-09-00. Pubmed ID: 37413951; DOI: 10.1016/j.scr.2023.103154 LCHi002-B 2023-09-00 2023-09-00 PubMed: 37413951 DOI: 10.1016/j.scr.2023.103154Associated cell lines:
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Feng Z, Yang X, Zhang H, Liu Y, Song W
Establishment of a controlled induced pluripotent stem cell line SDPHi004-A from a healthy male donor
Feng Z et al. Establishment of a controlled induced pluripotent stem cell line SDPHi004-A from a healthy male donor. . 2023-09-00. Pubmed ID: 37385132; DOI: 10.1016/j.scr.2023.103151 SDPHi004-A 2023-09-00 2023-09-00 PubMed: 37385132 DOI: 10.1016/j.scr.2023.103151Associated cell lines:
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Ben Yacoub T, Letellier C, Wohlschlegel J, Condroyer C, Slembrouck-Brec A, Goureau O, Zeitz C, Audo I
Generation of gene corrected human isogenic iPSC lines (IDVi003-A_CR13, IDVi003-A_CR21, IDVi003-A_CR24) from an inherited retinal dystrophy patient-derived IPSC line ITM2B-5286-3 (IDVi003-A) carrying the ITM2B c.782A > C variant using CRISPR/Cas9
Ben Yacoub T et al. Generation of gene corrected human isogenic iPSC lines (IDVi003-A_CR13, IDVi003-A_CR21, IDVi003-A_CR24) from an inherited retinal dystrophy patient-derived IPSC line ITM2B-5286-3 (IDVi003-A) carrying the ITM2B c.782A > C variant using CRISPR/Cas9. . 2023-09-00. Pubmed ID: 37473460; DOI: 10.1016/j.scr.2023.103166 IDVi003-AIDVi003-A-4IDVi003-A-5IDVi003-A-6 2023-09-00 2023-09-00 PubMed: 37473460 DOI: 10.1016/j.scr.2023.103166Associated cell lines:
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Gao L, Shi X, Su G, Guo Y, Lou Y, Wang Y, Miao P, Feng J
Generation of a human iPSC line (ZJSHDPi001-A) from peripheral blood mononuclear cells of a patient with Developmental epileptic encephalopathy-47 carrying FGF12 gene mutation (c.334G > A)
Gao L et al. Generation of a human iPSC line (ZJSHDPi001-A) from peripheral blood mononuclear cells of a patient with Developmental epileptic encephalopathy-47 carrying FGF12 gene mutation (c.334G > A). . 2023-09-00. Pubmed ID: 37331110; DOI: 10.1016/j.scr.2023.103127 ZJSHDPi001-A 2023-09-00 2023-09-00 PubMed: 37331110 DOI: 10.1016/j.scr.2023.103127Associated cell lines:
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Thongsin N, Suwanpitak S, Wattanapanitch M
CRISPR-Cas9-mediated disruption of B2M and CIITA genes eliminates HLA class I and II expression in human induced pluripotent stem cells (MUSIi001-A-2)
Thongsin N et al. CRISPR-Cas9-mediated disruption of B2M and CIITA genes eliminates HLA class I and II expression in human induced pluripotent stem cells (MUSIi001-A-2). . 2023-09-00. Pubmed ID: 37343428; DOI: 10.1016/j.scr.2023.103138 MUSIi001-AMUSIi001-A-1MUSIi001-A-2 2023-09-00 2023-09-00 PubMed: 37343428 DOI: 10.1016/j.scr.2023.103138Associated cell lines:
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Mazucanti CH, Kennedy V Jr, Premathilake HU, Doyle ME, Tian J, Liu QR, O'Connell J, Camandola S, Egan JM
AAV5-mediated manipulation of insulin expression in choroid plexus has long-term metabolic and behavioral consequences
Mazucanti CH et al. AAV5-mediated manipulation of insulin expression in choroid plexus has long-term metabolic and behavioral consequences. . 2023-08-29. Pubmed ID: 37515772; DOI: 10.1016/j.celrep.2023.112903; PMC: PMC10529429 WISCi004-B 2023-08-29 2023-08-29 PubMed: 37515772 DOI: 10.1016/j.celrep.2023.112903Associated cell lines:
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Faruqui N, Williams D, Briones A, Kepiro I, Ravi J, Kwan T, Mearns-Spragg A, Ryadnov M.
Extracellular matrix type 0: From ancient collagen lineage to a versatile product pipeline – JellaGel™
Faruqui N et al. Extracellular matrix type 0: From ancient collagen lineage to a versatile product pipeline – JellaGel™. . 2023-08-29. BIONi010-C 2023-08-29 2023-08-29Associated cell lines:
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Lee H, Aylward AJ, Pearse RV 2nd, Lish AM, Hsieh YC, Augur ZM, Benoit CR, Chou V, Knupp A, Pan C, Goberdhan S, Duong DM, Seyfried NT, Bennett DA, Taga MF, Huynh K, Arnold M, Meikle PJ, De Jager PL, Menon V, Young JE, Young-Pearse TL
Cell-type-specific regulation of APOE and CLU levels in human neurons by the Alzheimer's disease risk gene SORL1
Lee H et al. Cell-type-specific regulation of APOE and CLU levels in human neurons by the Alzheimer's disease risk gene SORL1. . 2023-08-29. Pubmed ID: 37611586; DOI: 10.1016/j.celrep.2023.112994; PMC: PMC10568487 HVRDi002-A 2023-08-29 2023-08-29 PubMed: 37611586 DOI: 10.1016/j.celrep.2023.112994Associated cell lines:
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Nutma E, Fancy N, Weinert M, Tsartsalis S, Marzin MC, Muirhead RCJ, Falk I, Breur M, de Bruin J, Hollaus D, Pieterman R, Anink J, Story D, Chandran S, Tang J, Trolese MC, Saito T, Saido TC, Wiltshire KH, Beltran-Lobo P, Phillips A, Antel J, Healy L, Dorion MF, Galloway DA, Benoit RY, Amossé Q, Ceyzériat K, Badina AM, Kövari E, Bendotti C, Aronica E, Radulescu CI, Wong JH, Barron AM, Smith AM, Barnes SJ, Hampton DW, van der Valk P, Jacobson S, Howell OW, Baker D, Kipp M, Kaddatz H, Tournier BB, Millet P, Matthews PM, Moore CS, Amor S, Owen DR
Translocator protein is a marker of activated microglia in rodent models but not human neurodegenerative diseases
Nutma E et al. Translocator protein is a marker of activated microglia in rodent models but not human neurodegenerative diseases. . 2023-08-28. Pubmed ID: 37640701; DOI: 10.1038/s41467-023-40937-z; PMC: PMC10462763 STBCi044-A 2023-08-28 2023-08-28 PubMed: 37640701 DOI: 10.1038/s41467-023-40937-zAssociated cell lines:
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Kizub I. V.
Induced pluripotent stem cells for cardiovascular therapeutics: Progress and perspectives
Kizub I. V.. Induced pluripotent stem cells for cardiovascular therapeutics: Progress and perspectives. . 2023-08-28. DOI: 10.15421/10.15421/022366 FAMRCi006-AFAMRCi006-BXACHi007-AXACHi008-AXACHi009-AUCSCi002-A 2023-08-28 2023-08-28 DOI: 10.15421/10.15421/022366Associated cell lines:
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Bauer Lisa, Giussani Stefania, Palazzi Nicola, Zare Farnaz, Colombo Elisa, Pinci Francesca, Leijten Lonneke, Smeenk Hilde, Embregts Carmen W.E., Silva Malan, Spoor Jochem K.H., Dirven Clemens, Gao Zhenyu, Bolleboom Anne, Verstrepen Babs E., Schuele Leonard, de Vrij Femke M.S., Kushner Steven A., Oude Munnink Bas B., Davila-Velderrain Jose, van Riel Debby, Harschnitz Oliver
Dissecting the neurotropism and neurovirulence of MPXV using human stem cell-based models
Bauer Lisa et al. Dissecting the neurotropism and neurovirulence of MPXV using human stem cell-based models. . 2023-08-28. DOI: 10.1101/2023.08.25.554849 WAe009-AWAe009-A-19 2023-08-28 2023-08-28 DOI: 10.1101/2023.08.25.554849Associated cell lines:
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Aguirre Marisol, Escobar Manuela, Forero Amézquita Sebastián, Cubillos David, Rincón Camilo, Vanegas Paula, Tarazona María Paula, Atuesta Escobar Sofía, Blanco Juan Camilo, Celis Luis Gustavo
Application of the Yamanaka Transcription Factors Oct4, Sox2, Klf4, and c-Myc from the Laboratory to the Clinic
Aguirre Marisol et al. Application of the Yamanaka Transcription Factors Oct4, Sox2, Klf4, and c-Myc from the Laboratory to the Clinic. . 2023-08-26. DOI: 10.3390/genes14091697 SDPHi002-A 2023-08-26 2023-08-26 DOI: 10.3390/genes14091697Associated cell lines:
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Muangsanit Papon, Chailangkarn Thanathom, Tanwattana Nathiphat, Wongwanakul Ratjika, Lekcharoensuk Porntippa, Kaewborisuth Challika
Hydrogel-based 3D human iPSC-derived neuronal culture for the study of rabies virus infection
Muangsanit Papon et al. Hydrogel-based 3D human iPSC-derived neuronal culture for the study of rabies virus infection. . 2023-08-25. DOI: 10.3389/fcimb.2023.1215205 MUSIi011-AMUSIi011-B 2023-08-25 2023-08-25 DOI: 10.3389/fcimb.2023.1215205Associated cell lines:
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Dey Subhasis, Patel Anjali, Haloi Nandan, Srimayee Soumya, Paul Suman, Barik Ganesh Kumar, Akhtar Nasim, Shaw Dipanjan, Hazarika Gunanka, Prusty Biswa Mohan, Kumar Mohit, Santra Manas Kumar, Tajkhorshid Emad, Bhattacharjee Surajit, Manna Debasis
Quinoline Thiourea-Based Zinc Ionophores with Antibacterial Activity
Dey Subhasis et al. Quinoline Thiourea-Based Zinc Ionophores with Antibacterial Activity. . 2023-08-24. DOI: 10.1021/acs.jmedchem.3c00368 NIMHi002-ANIMHi003-A 2023-08-24 2023-08-24 DOI: 10.1021/acs.jmedchem.3c00368Associated cell lines:
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Kislova Anastasiia V., Zheglo Diana, Pozhitnova Victoria O., Sviridov Philipp S., Gadzhieva Elmira P., Voronina Ekaterina S.
Replication stress causes delayed mitotic entry and chromosome 12 fragility at the ANKS1B large neuronal gene in human induced pluripotent stem cells
Kislova Anastasiia V. et al. Replication stress causes delayed mitotic entry and chromosome 12 fragility at the ANKS1B large neuronal gene in human induced pluripotent stem cells. . 2023-08-19. DOI: 10.1007/s10577-023-09729-5 RCMGi001-ARCMGi005-A 2023-08-19 2023-08-19 DOI: 10.1007/s10577-023-09729-5Associated cell lines:
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Fruhwürth S, Reinert LS, Öberg C, Sakr M, Henricsson M, Zetterberg H, Paludan SR
TREM2 is down-regulated by HSV1 in microglia and involved in antiviral defense in the brain
Fruhwürth S et al. TREM2 is down-regulated by HSV1 in microglia and involved in antiviral defense in the brain. . 2023-08-18. Pubmed ID: 37595041; DOI: 10.1126/sciadv.adf5808; PMC: PMC10438464 WTSIi015-A 2023-08-18 2023-08-18 PubMed: 37595041 DOI: 10.1126/sciadv.adf5808Associated cell lines:
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Liantonio Antonella, Bertini Matteo, Mele Antonietta, Balla Cristina, Dinoi Giorgia, Selvatici Rita, Mele Marco, De Luca Annamaria, Gualandi Francesca, Imbrici Paola
Brugada Syndrome: More than a Monogenic Channelopathy
Liantonio Antonella et al. Brugada Syndrome: More than a Monogenic Channelopathy. . 2023-08-18. DOI: 10.3390/biomedicines11082297 BBANTWi006-ABBANTWi007-A 2023-08-18 2023-08-18 DOI: 10.3390/biomedicines11082297Associated cell lines:
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Sheveleva Olga, Protasova Elena, Nenasheva Tatiana, Butorina Nina, Melnikova Victoria, Gerasimova Tatiana, Sakovnich Olga, Kurinov Alexander, Grigor’eva Elena, Medvedev Sergey, Lyadova Irina
A Model of iPSC-Derived Macrophages with TNFAIP3 Overexpression Reveals the Peculiarities of TNFAIP3 Protein Expression and Function in Human Macrophages
Sheveleva Olga et al. A Model of iPSC-Derived Macrophages with TNFAIP3 Overexpression Reveals the Peculiarities of TNFAIP3 Protein Expression and Function in Human Macrophages. . 2023-08-16. DOI: 10.3390/ijms241612868 ICGi021-AICGi022-A 2023-08-16 2023-08-16 DOI: 10.3390/ijms241612868 -
Shum IO, Merkert S, Malysheva S, Jahn K, Lachmann N, Verboom M, Frieling H, Hallensleben M, Martin U
An Improved Protocol for Targeted Differentiation of Primed Human Induced Pluripotent Stem Cells into HLA-G-Expressing Trophoblasts to Enable the Modeling of Placenta-Related Disorders
Shum IO et al. An Improved Protocol for Targeted Differentiation of Primed Human Induced Pluripotent Stem Cells into HLA-G-Expressing Trophoblasts to Enable the Modeling of Placenta-Related Disorders. . 2023-08-15. Pubmed ID: 37626882; DOI: 10.3390/cells12162070; PMC: PMC10453333 MHHi007-A 2023-08-15 2023-08-15 PubMed: 37626882 DOI: 10.3390/cells12162070Associated cell lines:
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Lassé M, El Saghir J, Berthier CC, Eddy S, Fischer M, Laufer SD, Kylies D, Hutzfeldt A, Bonin LL, Dumoulin B, Menon R, Vega-Warner V, Eichinger F, Alakwaa F, Fermin D, Billing AM, Minakawa A, McCown PJ, Rose MP, Godfrey B, Meister E, Wiech T, Noriega M, Chrysopoulou M, Brandts P, Ju W, Reinhard L, Hoxha E, Grahammer F, Lindenmeyer MT, Huber TB, Schlüter H, Thiel S, Mariani LH, Puelles VG, Braun F, Kretzler M, Demir F, Harder JL, Rinschen MM
An integrated organoid omics map extends modeling potential of kidney disease
Lassé M et al. An integrated organoid omics map extends modeling potential of kidney disease. . 2023-08-14. Pubmed ID: 37580326; DOI: 10.1038/s41467-023-39740-7; PMC: PMC10425428 UKEi001-A 2023-08-14 2023-08-14 PubMed: 37580326 DOI: 10.1038/s41467-023-39740-7Associated cell lines:
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Fan Yuhang, Si Zhibo, Wang Linlin, Zhang Lei
DYT-TOR1A dystonia: an update on pathogenesis and treatment
Fan Yuhang et al. DYT-TOR1A dystonia: an update on pathogenesis and treatment. . 2023-08-10. DOI: 10.3389/fnins.2023.1216929 CSUi002-ACSUi002-A-1 2023-08-10 2023-08-10 DOI: 10.3389/fnins.2023.1216929Associated cell lines:
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Binó L, Čajánek L
Tau tubulin kinase 1 and 2 regulate ciliogenesis and human pluripotent stem cells-derived neural rosettes
Binó L et al. Tau tubulin kinase 1 and 2 regulate ciliogenesis and human pluripotent stem cells-derived neural rosettes. . 2023-08-09. Pubmed ID: 37558899; DOI: 10.1038/s41598-023-39887-9; PMC: PMC10412607 MUNIe007-A 2023-08-09 2023-08-09 PubMed: 37558899 DOI: 10.1038/s41598-023-39887-9Associated cell lines:
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Noh JM, Choi SC, Song MH, Kim KS, Jun S, Park JH, Kim JH, Kim K, Ko TH, Choi JI, Gim JA, Kim JH, Jang Y, Park Y, Na JE, Rhyu IJ, Lim DS
The Activation of the LIMK/Cofilin Signaling Pathway via Extracellular Matrix-Integrin Interactions Is Critical for the Generation of Mature and Vascularized Cardiac Organoids
Noh JM et al. The Activation of the LIMK/Cofilin Signaling Pathway via Extracellular Matrix-Integrin Interactions Is Critical for the Generation of Mature and Vascularized Cardiac Organoids. . 2023-08-09. Pubmed ID: 37626839; DOI: 10.3390/cells12162029; PMC: PMC10453200 TMOi001-A 2023-08-09 2023-08-09 PubMed: 37626839 DOI: 10.3390/cells12162029Associated cell lines:
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Gomez-Sequeda Nicolas, Mendivil-Perez Miguel, Jimenez-Del-Rio Marlene, Lopera Francisco, Velez-Pardo Carlos
Cholinergic-like neurons and cerebral spheroids bearing the PSEN1 p.Ile416Thr variant mirror Alzheimer's disease neuropathology
Gomez-Sequeda Nicolas et al. Cholinergic-like neurons and cerebral spheroids bearing the PSEN1 p.Ile416Thr variant mirror Alzheimer's disease neuropathology. . 2023-08-08. DOI: 10.1038/s41598-023-39630-4 IMEDEAi006-A 2023-08-08 2023-08-08 DOI: 10.1038/s41598-023-39630-4Associated cell lines:
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Patterson Benjamin, Yang Bing, Tanaka Yoshiaki, Kim Kun-Yong, Cakir Bilal, Xiang Yangfei, Kim Jonghun, Wang Siyuan, Park In-Hyun
Female naïve human pluripotent stem cells carry X chromosomes with Xa-like and Xi-like folding conformations
Patterson Benjamin et al. Female naïve human pluripotent stem cells carry X chromosomes with Xa-like and Xi-like folding conformations. . 2023-08-04. DOI: 10.1126/sciadv.adf2245 MDCi014-AMDCi014-B 2023-08-04 2023-08-04 DOI: 10.1126/sciadv.adf2245 -
Stelcer Ewelina, Jopek Karol, Blatkiewicz Malgorzata, Olechnowicz Anna, Kaminski Kacper, Szyszka Marta, Suchorska Wiktoria Maria, Rucinski Marcin
Gene expression profile of hiPSC-derived cells differentiated with growth factors, forskolin and conditioned medium from human adrenocortical cell line
Stelcer Ewelina et al. Gene expression profile of hiPSC-derived cells differentiated with growth factors, forskolin and conditioned medium from human adrenocortical cell line. . 2023-08-04. DOI: 10.17219/acem/168603 GPCCi001-A 2023-08-04 2023-08-04 DOI: 10.17219/acem/168603Associated cell lines:
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Zhang Yi, Peng Qifeng, Zhang Renjun, Li Chao, Xu Quangang, Xia Luming, Wang Youming, Liu Ping, Pan Hong
Advances in CRISPR/Cas-Based Strategies on Zoonosis
Zhang Yi et al. Advances in CRISPR/Cas-Based Strategies on Zoonosis. . 2023-08-03. DOI: 10.1155/2023/9098445 MCRIi001-AMCRIi001-A-1 2023-08-03 2023-08-03 DOI: 10.1155/2023/9098445Associated cell lines:
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Miguez A, Gomis C, Vila C, Monguió-Tortajada M, Fernández-García S, Bombau G, Galofré M, García-Bravo M, Sanders P, Fernández-Medina H, Poquet B, Salado-Manzano C, Roura S, Alberch J, Segovia JC, Allen ND, Borràs FE, Canals JM
Soluble mutant huntingtin drives early human pathogenesis in Huntington's disease
Miguez A et al. Soluble mutant huntingtin drives early human pathogenesis in Huntington's disease. . 2023-08-03. Pubmed ID: 37535170; DOI: 10.1007/s00018-023-04882-w; PMC: PMC10400696 GENEAe015-AGENEAe020-ACHDIi026-ACHDIi042-A 2023-08-03 2023-08-03 PubMed: 37535170 DOI: 10.1007/s00018-023-04882-wAssociated cell lines:
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Niggl E, Bouman A, Briere LC, Hoogenboezem RM, Wallaard I, Park J, Admard J, Wilke M, Harris-Mostert EDRO, Elgersma M, Bain J, Balasubramanian M, Banka S, Benke PJ, Bertrand M, Blesson AE, Clayton-Smith J, Ellingford JM, Gillentine MA, Goodloe DH, Haack TB, Jain M, Krantz I, Luu SM, McPheron M, Muss CL, Raible SE, Robin NH, Spiller M, Starling S, Sweetser DA, Thiffault I, Vetrini F, Witt D, Woods E, Zhou D, Genomics England Research Consortium, Undiagnosed Diseases Network, Elgersma Y, van Esbroeck ACM
HNRNPC haploinsufficiency affects alternative splicing of intellectual disability-associated genes and causes a neurodevelopmental disorder
Niggl E et al. HNRNPC haploinsufficiency affects alternative splicing of intellectual disability-associated genes and causes a neurodevelopmental disorder. . 2023-08-03. Pubmed ID: 37541189; DOI: 10.1016/j.ajhg.2023.07.005; PMC: PMC10432175 EMCi169-AEMCi225-AEMCi169-BEMCi169-CEMCi169-DEMCi225-BEMCi225-CEMCi225-D 2023-08-03 2023-08-03 PubMed: 37541189 DOI: 10.1016/j.ajhg.2023.07.005 -
Noh J, Choi S, Song M, Kim K, Jun S, Park J, Kim J, Kim K, Ko T, Choi J, Gim J, Kim J, Jang Y, Park Y, Na J, Rhyu I, Lim D.
The Activation of the LIMK/Cofilin Signaling Pathway via Extracellular Matrix–Integrin Interactions Is Critical for the Generation of Mature and Vascularized Cardiac Organoids
Noh J et al. The Activation of the LIMK/Cofilin Signaling Pathway via Extracellular Matrix–Integrin Interactions Is Critical for the Generation of Mature and Vascularized Cardiac Organoids. . 2023-08-01. TMOi001-A 2023-08-01 2023-08-01Associated cell lines:
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Ariyasinghe NR, de Souza Santos R, Gross A, Aghamaleky-Sarvestany A, Kreimer S, Escopete S, Parker SJ, Sareen D
Proteomics of novel induced pluripotent stem cell-derived vascular endothelial cells reveal extensive similarity with an immortalized human endothelial cell line
Ariyasinghe NR et al. Proteomics of novel induced pluripotent stem cell-derived vascular endothelial cells reveal extensive similarity with an immortalized human endothelial cell line. . 2023-08-01. Pubmed ID: 37306406; DOI: 10.1152/physiolgenomics.00166.2022; PMC: PMC10396221 EDi028-AEDi042-A 2023-08-01 2023-08-01 PubMed: 37306406 DOI: 10.1152/physiolgenomics.00166.2022 -
Fan Yu, Li Meng-jie, Yang Jing, Li Shuang-jie, Hao Xiao-yan, Li Jia-di, Wang Yun-chao, Tang Mi-bo, Zhang Chan, Shi Jing-jing, Ma Dong-rui, Guo Meng-nan, Liu Fen, Shen Si, Yao Da-bao, Zuo Chun-yan, Mao Cheng-yuan, Hu Zheng-wei, Zhang Shuo, Yang Zhi-hua, Guo Guang-yu, Yang Jing-hua, Xia Zong-ping, Xu Yu-ming, Shi Chang-he
GGC repeat expansion in NOTCH2NLC induces dysfunction in ribosome biogenesis and translation
Fan Yu et al. GGC repeat expansion in NOTCH2NLC induces dysfunction in ribosome biogenesis and translation. . 2023-08-01. DOI: 10.1093/brain/awad058 ZZUi036-A 2023-08-01 2023-08-01 DOI: 10.1093/brain/awad058Associated cell lines:
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Sinner P, Peckert-Maier K, Mohammadian H, Kuhnt C, Draßner C, Panagiotakopoulou V, Rauber S, Linnerbauer M, Haimon Z, Royzman D, Kronenberg-Versteeg D, Ramming A, Steinkasserer A, Wild AB
Microglial expression of CD83 governs cellular activation and restrains neuroinflammation in experimental autoimmune encephalomyelitis
Sinner P et al. Microglial expression of CD83 governs cellular activation and restrains neuroinflammation in experimental autoimmune encephalomyelitis. . 2023-08-01. Pubmed ID: 37528070; DOI: 10.1038/s41467-023-40370-2; PMC: PMC10394088 BIONi010-CBIONi037-A 2023-08-01 2023-08-01 PubMed: 37528070 DOI: 10.1038/s41467-023-40370-2Associated cell lines:
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Buijsen Ronald A.M., Hu Michel, Sáez‐González Maria, Notopoulou Sofia, Mina Eleni, Koning Winette, Gardiner Sarah L., van der Graaf Linda M., Daoutsali Elena, Pepers Barry A., Mei Hailiang, van Dis Vera, Frimat Jean‐Philippe, van den Maagdenberg Arn M. J. M., Petrakis Spyros, van Roon‐Mom Willeke M.C.
Spinocerebellar Ataxia Type 1 Characteristics in Patient‐Derived Fibroblast and
Buijsen Ronald A.M. et al. Spinocerebellar Ataxia Type 1 Characteristics in Patient‐Derived Fibroblast andiPSC ‐Derived Neuronal CulturesiPSC ‐Derived Neuronal Cultures. . 2023-08-00. DOI: 10.1002/mds.29446 LUMCi002-ALUMCi003-ALUMCi005-ALUMCi007-ALUMCi008-A 2023-08-00 2023-08-00 DOI: 10.1002/mds.29446Associated cell lines:
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Tracey TJ, Jiang L, Gill MK, Ranie SN, Ovchinnikov DA, Wolvetang EJ, Ngo ST
Generation of a human induced pluripotent stem cell line (UQi001-A-1) edited with the CRISPR-Cas9 system to carry the heterozygous TARDBP c.1144G > A (p.A382T) missense mutation
Tracey TJ et al. Generation of a human induced pluripotent stem cell line (UQi001-A-1) edited with the CRISPR-Cas9 system to carry the heterozygous TARDBP c.1144G > A (p.A382T) missense mutation. . 2023-08-00. Pubmed ID: 37315423; DOI: 10.1016/j.scr.2023.103137 UQi001-AUQi001-A-1 2023-08-00 2023-08-00 PubMed: 37315423 DOI: 10.1016/j.scr.2023.103137Associated cell lines:
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Cheng Yu‐Shan, Xu Miao, Chen Guibin, Beers Jeanette, Chen Catherine Z., Liu Chengyu, Zou Jizhong, Zheng Wei
A Protocol for Culture and Characterization of Human Induced Pluripotent Stem Cells After Induction
Cheng Yu‐Shan et al. A Protocol for Culture and Characterization of Human Induced Pluripotent Stem Cells After Induction. . 2023-08-00. DOI: 10.1002/cpz1.866 TRNDi007-BTRNDi001-DTRNDi021-CTRNDi023-DTRNDi024-DTRNDi025-A 2023-08-00 2023-08-00 DOI: 10.1002/cpz1.866Associated cell lines:
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Quan Yingyi, Hu Minjie, Jiang Jiang, Jin Peifeng, Fan Junming, Li Ming, Fan Xiaofang, Gong Yongsheng, Yang Yang, Wang Yongyu
VGLL4 promotes vascular endothelium specification via TEAD1 in the vascular organoids and human pluripotent stem cells-derived endothelium model
Quan Yingyi et al. VGLL4 promotes vascular endothelium specification via TEAD1 in the vascular organoids and human pluripotent stem cells-derived endothelium model. . 2023-08-00. DOI: 10.1007/s00018-023-04858-w WAe001-AWAe001-A-47 2023-08-00 2023-08-00 DOI: 10.1007/s00018-023-04858-wAssociated cell lines:
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Pilotto Federica, Douthwaite Christopher, Diab Rim, Ye XiaoQian, Al qassab Zahraa, Tietje Christoph, Mounassir Meriem, Odriozola Adolfo, Thapa Aishwarya, Buijsen Ronald A.M., Lagache Sophie, Uldry Anne-Christine, Heller Manfred, Müller Stefan, van Roon-Mom Willeke M.C., Zuber Benoît, Liebscher Sabine, Saxena Smita
Early molecular layer interneuron hyperactivity triggers Purkinje neuron degeneration in SCA1
Pilotto Federica et al. Early molecular layer interneuron hyperactivity triggers Purkinje neuron degeneration in SCA1. . 2023-08-00. DOI: 10.1016/j.neuron.2023.05.016 LUMCi002-ALUMCi003-A 2023-08-00 2023-08-00 DOI: 10.1016/j.neuron.2023.05.016Associated cell lines:
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Ura H, Togi S, Ozaki M, Hatanaka H, Niida Y
Establishment of human induced pluripotent stem cell lines, KMUGMCi006, from a patient with Tuberous sclerosis complex (TSC) bearing mosaic nonsense mutations in the Tuberous sclerosis complex 2 (TSC2) gene
Ura H et al. Establishment of human induced pluripotent stem cell lines, KMUGMCi006, from a patient with Tuberous sclerosis complex (TSC) bearing mosaic nonsense mutations in the Tuberous sclerosis complex 2 (TSC2) gene. . 2023-08-00. Pubmed ID: 37271041; DOI: 10.1016/j.scr.2023.103129 KMUGMCi006-AKMUGMCi006-BKMUGMCi006-CKMUGMCi006-DKMUGMCi006-EKMUGMCi006-F 2023-08-00 2023-08-00 PubMed: 37271041 DOI: 10.1016/j.scr.2023.103129Associated cell lines:
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Chitrangi S, Vaity P, Jamdar A, Sarkar J, Bhatt S
Derivation of Breast Cancer Patient Derived Human Induced Pluripotent Stem Cell Line (YBLi006-A) with FANC-BRCA Gene Mutations: A Resource for Precision & Personalized Medicine
Chitrangi S et al. Derivation of Breast Cancer Patient Derived Human Induced Pluripotent Stem Cell Line (YBLi006-A) with FANC-BRCA Gene Mutations: A Resource for Precision & Personalized Medicine. . 2023-08-00. Pubmed ID: 37290137; DOI: 10.1016/j.scr.2023.103128 YBLi006-A 2023-08-00 2023-08-00 PubMed: 37290137 DOI: 10.1016/j.scr.2023.103128Associated cell lines:
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Liu Wen-Xiang, Li Chun-Xiao, Xie Xin-Xiang, Ge Wei, Qiao Tian, Sun Xiao-Feng, Shen Wei, Cheng Shun-Feng
Transcriptomic landscape reveals germline potential of porcine skin-derived multipotent dermal fibroblast progenitors
Liu Wen-Xiang et al. Transcriptomic landscape reveals germline potential of porcine skin-derived multipotent dermal fibroblast progenitors. . 2023-08-00. DOI: 10.1007/s00018-023-04869-7 CSUi004-A 2023-08-00 2023-08-00 DOI: 10.1007/s00018-023-04869-7Associated cell lines:
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Kondrateva E, Grigorieva O, Kurshakova E, Panchuk I, Pozhitnova V, Voronina E, Tabakov V, Orlova M, Lavrov A, Smirnikhina S, Kutsev S
Generation of induced pluripotent stem cell line (RCMGi009-A) from urine cells of patient with fibrodysplasia ossificans progressiva
Kondrateva E et al. Generation of induced pluripotent stem cell line (RCMGi009-A) from urine cells of patient with fibrodysplasia ossificans progressiva. . 2023-08-00. Pubmed ID: 37307755; DOI: 10.1016/j.scr.2023.103133 RCMGi009-A 2023-08-00 2023-08-00 PubMed: 37307755 DOI: 10.1016/j.scr.2023.103133Associated cell lines:
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Velicky P, Miguel E, Michalska JM, Lyudchik J, Wei D, Lin Z, Watson JF, Troidl J, Beyer J, Ben-Simon Y, Sommer C, Jahr W, Cenameri A, Broichhagen J, Grant SGN, Jonas P, Novarino G, Pfister H, Bickel B, Danzl JG
Dense 4D nanoscale reconstruction of living brain tissue
Velicky P et al. Dense 4D nanoscale reconstruction of living brain tissue. . 2023-08-00. Pubmed ID: 37429995; DOI: 10.1038/s41592-023-01936-6; PMC: PMC10406607 WAe009-A 2023-08-00 2023-08-00 PubMed: 37429995 DOI: 10.1038/s41592-023-01936-6Associated cell lines:
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Lahm H, Dzilic E, Neb I, Doppler SA, Schneider S, Lange R, Krane M, Dreßen M
Correction of a deleterious TBX5 mutation in an induced pluripotent stem cell line (DHMi004-A-1) using a completely plasmid-free CRISPR/Cas 9 approach
Lahm H et al. Correction of a deleterious TBX5 mutation in an induced pluripotent stem cell line (DHMi004-A-1) using a completely plasmid-free CRISPR/Cas 9 approach. . 2023-08-00. Pubmed ID: 37253295; DOI: 10.1016/j.scr.2023.103126 DHMi004-ADHMi004-A-1 2023-08-00 2023-08-00 PubMed: 37253295 DOI: 10.1016/j.scr.2023.103126Associated cell lines:
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Wang H, Guo T, Lan F
Generation of a human embryonic stem cell line WAe009-A-79 carrying a long QT syndrome mutation in KCNQ1
Wang H et al. Generation of a human embryonic stem cell line WAe009-A-79 carrying a long QT syndrome mutation in KCNQ1. . 2023-08-00. Pubmed ID: 37244124; DOI: 10.1016/j.scr.2023.103119 WAe009-AWAe009-A-79 2023-08-00 2023-08-00 PubMed: 37244124 DOI: 10.1016/j.scr.2023.103119Associated cell lines:
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Jiang Z, Sun W, Zhang Q, Wang P
Generation of an induced pluripotent stem cell line (ZSZOCi001-A) from a patient with Knobloch syndrome caused by biallelic mutations in the gene COL18A1
Jiang Z et al. Generation of an induced pluripotent stem cell line (ZSZOCi001-A) from a patient with Knobloch syndrome caused by biallelic mutations in the gene COL18A1. . 2023-08-00. Pubmed ID: 37269665; DOI: 10.1016/j.scr.2023.103131 ZSZOCi001-A 2023-08-00 2023-08-00 PubMed: 37269665 DOI: 10.1016/j.scr.2023.103131Associated cell lines:
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Li Y, Wan Z, Wang B, Zhang H, Guan J, Yang X, Jin X, Ma X, Liu Y
Generation of JAG1 gene c.1615C > T heterozygous mutation human embryonic stem cell line (SDQLCHe001-A) using cytosine base editor
Li Y et al. Generation of JAG1 gene c.1615C > T heterozygous mutation human embryonic stem cell line (SDQLCHe001-A) using cytosine base editor. . 2023-08-00. Pubmed ID: 37245339; DOI: 10.1016/j.scr.2023.103120 SDQLCHe001-A 2023-08-00 2023-08-00 PubMed: 37245339 DOI: 10.1016/j.scr.2023.103120Associated cell lines:
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Du Weibin, Hu Jintao, Huang Xiaolong, Wang Zhenwei, Zhou Huateng, Yang Yadong, Hu Huahui, Chen Rongliang, Shen Fuxiang, Quan Renfu
Feasibility of repairing skin defects by
Du Weibin et al. Feasibility of repairing skin defects byVEGF165 gene‐modifiediPS‐HFSCs seeded on a3D printed scaffold containing astragalus polysaccharideVEGF165 gene‐modifiediPS‐HFSCs seeded on a3D printed scaffold containing astragalus polysaccharide. . 2023-08-00. DOI: 10.1111/jcmm.17800 SHFDi001-AUNIGEi003-AICGi040-A 2023-08-00 2023-08-00 DOI: 10.1111/jcmm.17800Associated cell lines:
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Tripathi Manish Kumar, Ojha Shashank Kumar, Kartawy Maryam, Hamoudi Wajeha, Choudhary Ashwani, Stern Shani, Aran Adi, Amal Haitham
The NO Answer for Autism Spectrum Disorder
Tripathi Manish Kumar et al. The NO Answer for Autism Spectrum Disorder. . 2023-08-00. DOI: 10.1002/advs.202205783 UOHi002-AUOHi003-A 2023-08-00 2023-08-00 DOI: 10.1002/advs.202205783 -
Cui S, Shin YJ, Fang X, Lee H, Eum SH, Ko EJ, Lim SW, Shin E, Lee KI, Lee JY, Lee CB, Bae SK, Yang CW, Chung BH
CRISPR/Cas9-mediated A4GALT suppression rescues Fabry disease phenotypes in a kidney organoid model
Cui S et al. CRISPR/Cas9-mediated A4GALT suppression rescues Fabry disease phenotypes in a kidney organoid model. . 2023-08-00. Pubmed ID: 36805562; DOI: 10.1016/j.trsl.2023.02.005 CMCi002-ACMCi006-ACMCi007-A 2023-08-00 2023-08-00 PubMed: 36805562 DOI: 10.1016/j.trsl.2023.02.005 -
Nimonkar MM, Arunachal G, Dash SS, Kandy SK, Raghavendra K, Chetan GK, Mehta B, Markandeya YS
Generation and characterisation of a human induced pluripotent stem cell line, NIMHi007-A, from peripheral blood mononuclear cells derived from an adult healthy female
Nimonkar MM et al. Generation and characterisation of a human induced pluripotent stem cell line, NIMHi007-A, from peripheral blood mononuclear cells derived from an adult healthy female. . 2023-08-00. Pubmed ID: 37269666; DOI: 10.1016/j.scr.2023.103130 NIMHi007-A 2023-08-00 2023-08-00 PubMed: 37269666 DOI: 10.1016/j.scr.2023.103130Associated cell lines:
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Soussi Salwa, Savchenko Lesia, Rovina Davide, Iacovoni Jason S., Gottinger Andrea, Vialettes Maxime, Pioner Josè-Manuel, Farini Andrea, Mallia Sara, Rabino Martina, Pompilio Giulio, Parini Angelo, Lairez Olivier, Gowran Aoife, Pizzinat Nathalie
IPSC derived cardiac fibroblasts of DMD patients show compromised actin microfilaments, metabolic shift and pro-fibrotic phenotype
Soussi Salwa et al. IPSC derived cardiac fibroblasts of DMD patients show compromised actin microfilaments, metabolic shift and pro-fibrotic phenotype. . 2023-07-27. DOI: 10.1186/s13062-023-00398-2 CCMi003-ACCMi005-A 2023-07-27 2023-07-27 DOI: 10.1186/s13062-023-00398-2 -
Asmar AJ, Abrams SR, Hsin J, Collins JC, Yazejian RM, Wu Y, Cho J, Doyle AD, Cinthala S, Simon M, van Jaarsveld RH, Beck DB, Kerosuo L, Werner A
A ubiquitin-based effector-to-inhibitor switch coordinates early brain, craniofacial, and skin development
Asmar AJ et al. A ubiquitin-based effector-to-inhibitor switch coordinates early brain, craniofacial, and skin development. . 2023-07-26. Pubmed ID: 37495603; DOI: 10.1038/s41467-023-40223-y; PMC: PMC10371987 WAe001-A 2023-07-26 2023-07-26 PubMed: 37495603 DOI: 10.1038/s41467-023-40223-yAssociated cell lines:
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Calamaio S, Serzanti M, Boniotti J, Fra A, Garrafa E, Cominelli M, Verardi R, Poliani PL, Dotti S, Villa R, Mazzoleni G, Dell'Era P, Steimberg N
Human iPSC-Derived 3D Hepatic Organoids in a Miniaturized Dynamic Culture System
Calamaio S et al. Human iPSC-Derived 3D Hepatic Organoids in a Miniaturized Dynamic Culture System. . 2023-07-26. Pubmed ID: 37626611; DOI: 10.3390/biomedicines11082114; PMC: PMC10452373 TMOi001-A 2023-07-26 2023-07-26 PubMed: 37626611 DOI: 10.3390/biomedicines11082114Associated cell lines:
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Glaß Hannes, Jonitz-Heincke Anika, Petters Janine, Lukas Jan, Bader Rainer, Hermann Andreas
Corrosion Products from Metallic Implants Induce ROS and Cell Death in Human Motoneurons In Vitro
Glaß Hannes et al. Corrosion Products from Metallic Implants Induce ROS and Cell Death in Human Motoneurons In Vitro. . 2023-07-25. DOI: 10.3390/jfb14080392 AKOSi006-AAKOSi007-A 2023-07-25 2023-07-25 DOI: 10.3390/jfb14080392Associated cell lines:
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Heiland M, Connolly NMC, Mamad O, Nguyen NT, Kesavan JC, Langa E, Fanning K, Sanfeliu A, Yan Y, Su J, Venø MT, Costard LS, Neubert V, Engel T, Hill TDM, Freiman TM, Mahesh A, Tiwari VK, Rosenow F, Bauer S, Kjems J, Morris G, Henshall DC
MicroRNA-335-5p suppresses voltage-gated sodium channel expression and may be a target for seizure control
Heiland M et al. MicroRNA-335-5p suppresses voltage-gated sodium channel expression and may be a target for seizure control. . 2023-07-25. Pubmed ID: 37463203; DOI: 10.1073/pnas.2216658120; PMC: PMC10372546 WTSIi020-A 2023-07-25 2023-07-25 PubMed: 37463203 DOI: 10.1073/pnas.2216658120Associated cell lines:
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Ganizada BH, Reesink KD, Parikh S, Ramaekers MJFG, Akbulut AC, Saraber PJMH, Debeij GP, Mumc-Taa Student Team, Jaminon AM, Natour E, Lorusso R, Wildberger JE, Mees B, Schurink GW, Jacobs MJ, Cleutjens J, Krapels I, Gombert A, Maessen JG, Accord R, Delhaas T, Schalla S, Schurgers LJ, Bidar E
The Maastricht Acquisition Platform for Studying Mechanisms of Cell-Matrix Crosstalk (MAPEX): An Interdisciplinary and Systems Approach towards Understanding Thoracic Aortic Disease
Ganizada BH et al. The Maastricht Acquisition Platform for Studying Mechanisms of Cell-Matrix Crosstalk (MAPEX): An Interdisciplinary and Systems Approach towards Understanding Thoracic Aortic Disease. . 2023-07-25. Pubmed ID: 37626592; DOI: 10.3390/biomedicines11082095; PMC: PMC10452257 CARIMi004-A 2023-07-25 2023-07-25 PubMed: 37626592 DOI: 10.3390/biomedicines11082095Associated cell lines:
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Ganizada B, Reesink K, Parikh S, Ramaekers M, Akbulut A, Saraber P, Debeij G, MUMC-TAA Student Team, Jaminon A, Natour E, Lorusso R, Wildberger J, Mees B, Schurink G, Jacobs M, Cleutjens J, Krapels I, Gombert A, Maessen J, Accord R, Delhaas T, Schalla S, Schurgers L, Bidar E.
The Maastricht Acquisition Platform for Studying Mechanisms of Cell–Matrix Crosstalk (MAPEX): An Interdisciplinary and Systems Approach towards Understanding Thoracic Aortic Disease
Ganizada B et al. The Maastricht Acquisition Platform for Studying Mechanisms of Cell–Matrix Crosstalk (MAPEX): An Interdisciplinary and Systems Approach towards Understanding Thoracic Aortic Disease. . 2023-07-25. CARIMi004-A 2023-07-25 2023-07-25Associated cell lines:
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Trionfini P, Romano E, Varinelli M, Longaretti L, Rizzo P, Giampietro R, Caroli A, Aiello S, Todeschini M, Casiraghi F, Remuzzi G, Benigni A, Tomasoni S
Hypoimmunogenic Human Pluripotent Stem Cells as a Powerful Tool for Liver Regenerative Medicine
Trionfini P et al. Hypoimmunogenic Human Pluripotent Stem Cells as a Powerful Tool for Liver Regenerative Medicine. . 2023-07-22. Pubmed ID: 37511568; DOI: 10.3390/ijms241411810; PMC: PMC10380710 IRFMNi001-BIRFMNi001-B-1IRFMNi001-B-2 2023-07-22 2023-07-22 PubMed: 37511568 DOI: 10.3390/ijms241411810Associated cell lines:
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Meiser I, Alstrup M, Khalesi E, Stephan B, Speicher AM, Majer J, Kwok CK, Neubauer JC, Hansson M, Zimmermann H
Application-Oriented Bulk Cryopreservation of Human iPSCs in Cryo Bags Followed by Direct Inoculation in Scalable Suspension Bioreactors for Expansion and Neural Differentiation
Meiser I et al. Application-Oriented Bulk Cryopreservation of Human iPSCs in Cryo Bags Followed by Direct Inoculation in Scalable Suspension Bioreactors for Expansion and Neural Differentiation. . 2023-07-22. Pubmed ID: 37508576; DOI: 10.3390/cells12141914; PMC: PMC10378238 UKKi011-ABIONi010-CBIONi010-C-41 2023-07-22 2023-07-22 PubMed: 37508576 DOI: 10.3390/cells12141914Associated cell lines:
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Chitrangi Swati, Vaity Pooja, Jamdar Aishwarya, Bhatt Shweta
Patient-derived organoids for precision oncology: a platform to facilitate clinical decision making
Chitrangi Swati et al. Patient-derived organoids for precision oncology: a platform to facilitate clinical decision making. . 2023-07-22. DOI: 10.1186/s12885-023-11078-9 YBLi006-A 2023-07-22 2023-07-22 DOI: 10.1186/s12885-023-11078-9Associated cell lines:
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Allan A, Creech J, Hausner C, Krajcarski P, Gunawan B, Poulin N, Kozlowski P, Clark CW, Dow R, Saraithong P, Mair DB, Block T, Monteiro da Rocha A, Kim DH, Herron TJ
High-throughput longitudinal electrophysiology screening of mature chamber-specific hiPSC-CMs using optical mapping
Allan A et al. High-throughput longitudinal electrophysiology screening of mature chamber-specific hiPSC-CMs using optical mapping. . 2023-07-21. Pubmed ID: 37416454; DOI: 10.1016/j.isci.2023.107142; PMC: PMC10320609 UCSFi001-A 2023-07-21 2023-07-21 PubMed: 37416454 DOI: 10.1016/j.isci.2023.107142Associated cell lines:
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Beccano-Kelly DA, Cherubini M, Mousba Y, Cramb KML, Giussani S, Caiazza MC, Rai P, Vingill S, Bengoa-Vergniory N, Ng B, Corda G, Banerjee A, Vowles J, Cowley S, Wade-Martins R
Calcium dysregulation combined with mitochondrial failure and electrophysiological maturity converge in Parkinson's iPSC-dopamine neurons
Beccano-Kelly DA et al. Calcium dysregulation combined with mitochondrial failure and electrophysiological maturity converge in Parkinson's iPSC-dopamine neurons. . 2023-07-21. Pubmed ID: 37426342; DOI: 10.1016/j.isci.2023.107044; PMC: PMC10329047 UOXFi001-BUOXFi002-AUOXFi003-AUOXFi004-BUOXFi005-ASTBCi042-ASTBCi026-DSTBCi052-BSTBCi057-ASTBCi084-BSTBCi101-ASTBCi105-ASTBCi106-ASTBCi298-A 2023-07-21 2023-07-21 PubMed: 37426342 DOI: 10.1016/j.isci.2023.107044Associated cell lines:
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Mullari M, Fossat N, Skotte NH, Asenjo-Martinez A, Humphreys DT, Bukh J, Kirkeby A, Scheel TKH, Nielsen ML
Characterising the RNA-binding protein atlas of the mammalian brain uncovers RBM5 misregulation in mouse models of Huntington's disease
Mullari M et al. Characterising the RNA-binding protein atlas of the mammalian brain uncovers RBM5 misregulation in mouse models of Huntington's disease. . 2023-07-19. Pubmed ID: 37468457; DOI: 10.1038/s41467-023-39936-x; PMC: PMC10356804 RCe021-A 2023-07-19 2023-07-19 PubMed: 37468457 DOI: 10.1038/s41467-023-39936-xAssociated cell lines:
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Zhu Zeyu, Hou Wenzhe, Cao Yuwen, Zheng Haoran, Tian Wotu, Cao Li
Spastic paraplegia type 76 due to novel CAPN1 mutations: three case reports with literature review
Zhu Zeyu et al. Spastic paraplegia type 76 due to novel CAPN1 mutations: three case reports with literature review. . 2023-07-19. DOI: 10.1007/s10048-023-00726-8 FJMUi001-A 2023-07-19 2023-07-19 DOI: 10.1007/s10048-023-00726-8Associated cell lines:
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Lin JQ, Khuperkar D, Pavlou S, Makarchuk S, Patikas N, Lee FC, Zbiegly JM, Kang J, Field SF, Bailey DM, Freeman JL, Ule J, Metzakopian E, Ruepp MD, Mallucci GR
HNRNPH1 regulates the neuroprotective cold-shock protein RBM3 expression through poison exon exclusion
Lin JQ et al. HNRNPH1 regulates the neuroprotective cold-shock protein RBM3 expression through poison exon exclusion. . 2023-07-17. Pubmed ID: 37248947; DOI: 10.15252/embj.2022113168; PMC: PMC10350819 CAMi014-A 2023-07-17 2023-07-17 PubMed: 37248947 DOI: 10.15252/embj.2022113168Associated cell lines:
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Cao Shuo, Gao Xinyue, Liu Fangyuan, Chen Yanglin, Na Qin, Meng Qiaoqiao, Shao Peng, Chen Chen, Song Yongli, Wu Baojiang, Li Xihe, Bao Siqin
Derivation and characteristics of induced pluripotent stem cells from a patient with acute myelitis
Cao Shuo et al. Derivation and characteristics of induced pluripotent stem cells from a patient with acute myelitis. . 2023-07-14. DOI: 10.3389/fcell.2023.1172385 CSUASOi001-ACSUASOi003-A 2023-07-14 2023-07-14 DOI: 10.3389/fcell.2023.1172385Associated cell lines:
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Li Y, Ding J, Araki D, Zou J, Larochelle A
Modulation of WNT, Activin/Nodal, and MAPK Signaling Pathways Increases Arterial Hemogenic Endothelium and Hematopoietic Stem/Progenitor Cell Formation During Human iPSC Differentiation
Li Y et al. Modulation of WNT, Activin/Nodal, and MAPK Signaling Pathways Increases Arterial Hemogenic Endothelium and Hematopoietic Stem/Progenitor Cell Formation During Human iPSC Differentiation. . 2023-07-14. Pubmed ID: 37220178; DOI: 10.1093/stmcls/sxad040; PMC: PMC10346406 TRNDi009-CRTIBDi001-A 2023-07-14 2023-07-14 PubMed: 37220178 DOI: 10.1093/stmcls/sxad040Associated cell lines:
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Wichmann M, Maire CL, Nuppenau N, Habiballa M, Uhde A, Kolbe K, Schröder T, Lamszus K, Fehse B, Głów D
Deep Characterization and Comparison of Different Retrovirus-like Particles Preloaded with CRISPR/Cas9 RNPs
Wichmann M et al. Deep Characterization and Comparison of Different Retrovirus-like Particles Preloaded with CRISPR/Cas9 RNPs. . 2023-07-13. Pubmed ID: 37511168; DOI: 10.3390/ijms241411399; PMC: PMC10380221 BIHi001-B 2023-07-13 2023-07-13 PubMed: 37511168 DOI: 10.3390/ijms241411399Associated cell lines:
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Zhang Lin-ming, Chen Ling, Zhao Yi-fei, Duan Wei-mei, Zhong Lian-mei, Liu Ming-wei
Identification of key potassium channel genes of temporal lobe epilepsy by bioinformatics analyses and experimental verification
Zhang Lin-ming et al. Identification of key potassium channel genes of temporal lobe epilepsy by bioinformatics analyses and experimental verification. . 2023-07-07. DOI: 10.3389/fneur.2023.1175007 HIHDNEi003-A 2023-07-07 2023-07-07 DOI: 10.3389/fneur.2023.1175007Associated cell lines:
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Xue Mei
Case Report: Prenatal neurological injury in a neonate with pyruvate carboxylase deficiency type B
Xue Mei. Case Report: Prenatal neurological injury in a neonate with pyruvate carboxylase deficiency type B. . 2023-07-07. DOI: 10.3389/fendo.2023.1199590 SHCDNi007-A 2023-07-07 2023-07-07 DOI: 10.3389/fendo.2023.1199590Associated cell lines:
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Shi Yajun, Zhao Yan, Lu Likui, Gao Qinqin, Yu Dongyi, Sun Miao
CRISPR/Cas9: implication for modeling and therapy of amyotrophic lateral sclerosis
Shi Yajun et al. CRISPR/Cas9: implication for modeling and therapy of amyotrophic lateral sclerosis. . 2023-07-06. DOI: 10.3389/fnins.2023.1223777 WAe009-AWAe009-A-83 2023-07-06 2023-07-06 DOI: 10.3389/fnins.2023.1223777Associated cell lines:
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Hussein Yara, Tripathi Utkarsh, Choudhary Ashwani, Nayak Ritu, Peles David, Rosh Idan, Rabinski Tatiana, Djamus Jose, Vatine Gad David, Spiegel Ronen, Garin-Shkolnik Tali, Stern Shani
Early maturation and hyperexcitability is a shared phenotype of cortical neurons derived from different ASD-associated mutations
Hussein Yara et al. Early maturation and hyperexcitability is a shared phenotype of cortical neurons derived from different ASD-associated mutations. . 2023-07-06. DOI: 10.1038/s41398-023-02535-x UOHi002-AUOHi003-A 2023-07-06 2023-07-06 DOI: 10.1038/s41398-023-02535-x -
Farrawell Natalie E, Bax Monique, McAlary Luke, McKenna Jessie, Maksour Simon, Do-Ha Dzung, Rayner Stephanie L, Blair Ian P, Chung Roger S, Yerbury Justin J, Ooi Lezanne, Saunders Darren N
ALS-linked CCNF variant disrupts motor neuron ubiquitin homeostasis
Farrawell Natalie E et al. ALS-linked CCNF variant disrupts motor neuron ubiquitin homeostasis. . 2023-07-04. DOI: 10.1093/hmg/ddad063 UOWi005-A 2023-07-04 2023-07-04 DOI: 10.1093/hmg/ddad063Associated cell lines:
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Kerkering J, Muinjonov B, Rosiewicz KS, Diecke S, Biese C, Schiweck J, Chien C, Zocholl D, Conrad T, Paul F, Alisch M, Siffrin V
iPSC-derived reactive astrocytes from patients with multiple sclerosis protect cocultured neurons in inflammatory conditions
Kerkering J et al. iPSC-derived reactive astrocytes from patients with multiple sclerosis protect cocultured neurons in inflammatory conditions. . 2023-07-03. Pubmed ID: 37219933; DOI: 10.1172/jci164637; PMC: PMC10313373 BIHi002-ABIHi005-ABIHi242-ABIHi250-ABIHi005-A-24 2023-07-03 2023-07-03 PubMed: 37219933 DOI: 10.1172/jci164637Associated cell lines:
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Feathers Kecia L., Jia Lin, Khan Naheed W., Smith Alexander J., Ma Jian-Xing, Ali Robin R., Thompson Debra A.
Gene Supplementation in Mice Heterozygous for the D477G RPE65 Variant Implicated in Autosomal Dominant Retinitis Pigmentosa
Feathers Kecia L. et al. Gene Supplementation in Mice Heterozygous for the D477G RPE65 Variant Implicated in Autosomal Dominant Retinitis Pigmentosa. . 2023-07-01. DOI: 10.1089/hum.2022.240 NUIGi027-ANUIGi028-ANUIGi029-A 2023-07-01 2023-07-01 DOI: 10.1089/hum.2022.240Associated cell lines:
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Fus-Kujawa Agnieszka, Mendrek Barbara, Bajdak-Rusinek Karolina, Diak Natalia, Strzelec Karolina, Gutmajster Ewa, Janelt Kamil, Kowalczuk Agnieszka, Trybus Anna, Rozwadowska Patrycja, Wojakowski Wojciech, Gawron Katarzyna, Sieroń Aleksander L.
Gene-repaired iPS cells as novel approach for patient with osteogenesis imperfecta
Fus-Kujawa Agnieszka et al. Gene-repaired iPS cells as novel approach for patient with osteogenesis imperfecta. . 2023-06-30. DOI: 10.3389/fbioe.2023.1205122 INSRMi008-AINSRMi009-AINSRMi010-A 2023-06-30 2023-06-30 DOI: 10.3389/fbioe.2023.1205122Associated cell lines:
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Kidwai Fahad K., Canalis Ernesto, Robey Pamela G.
Induced pluripotent stem cell technology in bone biology
Kidwai Fahad K. et al. Induced pluripotent stem cell technology in bone biology. . 2023-07-00. DOI: 10.1016/j.bone.2023.116760 NIDCRi001-ASDQLCHi037-A 2023-07-00 2023-07-00 DOI: 10.1016/j.bone.2023.116760Associated cell lines:
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Carvalho LML, Branco EV, Sarafian RD, Kobayashi GS, de Araújo FT, Santos Souza L, Moreira DP, Hsia GSP, Bertollo EMG, Buck CB, da Costa SS, Fialho DM, de Vasconcelos FTGR, Brito LA, de Souza Fraga Machado LE, Ramos IC, Pereira LDV, Koiffmann CP, E Passos-Bueno MRDS, Oliveira Mendes TA, Krepischi ACV, Rosenberg C
Establishment of iPSC lines and zebrafish with loss-of-function AHDC1 variants: Models for Xia-Gibbs syndrome
Carvalho LML et al. Establishment of iPSC lines and zebrafish with loss-of-function AHDC1 variants: Models for Xia-Gibbs syndrome. . 2023-06-30. Pubmed ID: 37054903; DOI: 10.1016/j.gene.2023.147424 USPi001-AUSPi002-AUSPi003-ACEGHUi001-A 2023-06-30 2023-06-30 PubMed: 37054903 DOI: 10.1016/j.gene.2023.147424Associated cell lines:
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Lu Xinyi, Jin Hongzhong
A Review of CRISPR-Based Advances in Dermatological Diseases
Lu Xinyi et al. A Review of CRISPR-Based Advances in Dermatological Diseases. . 2023-07-00. DOI: 10.1007/s40291-023-00642-5 UQACi001-A 2023-07-00 2023-07-00 DOI: 10.1007/s40291-023-00642-5Associated cell lines:
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Zhou Bo, Wu Yuyang, Cheng Pei, Wu Chengyong
Long noncoding
Zhou Bo et al. Long noncodingRNAs with peptide‐encoding potential identified in esophageal squamous cell carcinoma: KDM4A‐AS1‐encoded peptide weakens cancer cell viability and migratory capacityRNAs with peptide‐encoding potential identified in esophageal squamous cell carcinoma: KDM4A‐AS1‐encoded peptide weakens cancer cell viability and migratory capacity. . 2023-07-00. DOI: 10.1002/1878-0261.13424 FDCHDPi001-A 2023-07-00 2023-07-00 DOI: 10.1002/1878-0261.13424Associated cell lines:
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Liu Zhen, Yan Weiwei, Liu Shaohua, Liu Zhan, Xu Ping, Fang Weiyi
Regulatory network and targeted interventions for CCDC family in tumor pathogenesis
Liu Zhen et al. Regulatory network and targeted interventions for CCDC family in tumor pathogenesis. . 2023-07-00. DOI: 10.1016/j.canlet.2023.216225 UHOMi001-A 2023-07-00 2023-07-00 DOI: 10.1016/j.canlet.2023.216225Associated cell lines:
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Forgham Helen, Liu Liwei, Zhu Jiayuan, Javed Ibrahim, Cai Weibo, Qiao Ruirui, Davis Thomas P.
Vector enabled CRISPR gene editing – A revolutionary strategy for targeting the diversity of brain pathologies
Forgham Helen et al. Vector enabled CRISPR gene editing – A revolutionary strategy for targeting the diversity of brain pathologies. . 2023-07-00. DOI: 10.1016/j.ccr.2023.215172 GIBHi002-AGIBHi002-A-5 2023-07-00 2023-07-00 DOI: 10.1016/j.ccr.2023.215172Associated cell lines:
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Waqas FH, Shehata M, Elgaher WAM, Lacour A, Kurmasheva N, Begnini F, Kiib AE, Dahlmann J, Chen C, Pavlou A, Poulsen TB, Merkert S, Martin U, Olmer R, Olagnier D, Hirsch AKH, Pleschka S, Pessler F
NRF2 activators inhibit influenza A virus replication by interfering with nucleo-cytoplasmic export of viral RNPs in an NRF2-independent manner
Waqas FH et al. NRF2 activators inhibit influenza A virus replication by interfering with nucleo-cytoplasmic export of viral RNPs in an NRF2-independent manner. . 2023-07-00. Pubmed ID: 37459366; DOI: 10.1371/journal.ppat.1011506; PMC: PMC10374058 MHHi001-A 2023-07-00 2023-07-00 PubMed: 37459366 DOI: 10.1371/journal.ppat.1011506Associated cell lines:
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Takahashi Masayuki, Furuya Naoko
Evaluation of the Effects of Power‐Frequency Magnetic Field Exposure on B‐Cell Differentiation From Human Hematopoietic Stem/Progenitor Cells
Takahashi Masayuki et al. Evaluation of the Effects of Power‐Frequency Magnetic Field Exposure on B‐Cell Differentiation From Human Hematopoietic Stem/Progenitor Cells. . 2023-07-00. DOI: 10.1002/bem.22447 IMSUTi002-AIMSUTi002-A-1 2023-07-00 2023-07-00 DOI: 10.1002/bem.22447Associated cell lines:
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Stančin P, Song MS, Alajbeg I, Mitrečić D
Human Oral Mucosa Stem Cells Increase Survival of Neurons Affected by In Vitro Anoxia and Improve Recovery of Mice Affected by Stroke Through Time-limited Secretion of miR-514A-3p
Stančin P et al. Human Oral Mucosa Stem Cells Increase Survival of Neurons Affected by In Vitro Anoxia and Improve Recovery of Mice Affected by Stroke Through Time-limited Secretion of miR-514A-3p. . 2023-07-00. Pubmed ID: 36083390; DOI: 10.1007/s10571-022-01276-7; PMC: PMC10287825 WTSIi189-A 2023-07-00 2023-07-00 PubMed: 36083390 DOI: 10.1007/s10571-022-01276-7Associated cell lines:
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Roshandel Danial, Semnani Farbod, Rayati Damavandi Amirmasoud, Masoudi Ali, Baradaran-Rafii Alireza, Watson Stephanie L., Morgan William H., McLenachan Samuel
Genetic predisposition to ocular surface disorders and opportunities for gene-based therapies
Roshandel Danial et al. Genetic predisposition to ocular surface disorders and opportunities for gene-based therapies. . 2023-07-00. DOI: 10.1016/j.jtos.2023.05.003 UNIPDi003-AUCLi013-A 2023-07-00 2023-07-00 DOI: 10.1016/j.jtos.2023.05.003Associated cell lines:
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Soroka AB, Feoktistova SG, Mityaeva ON, Volchkov PY
Gene Therapy Approaches for the Treatment of Hemophilia B
Soroka AB et al. Gene Therapy Approaches for the Treatment of Hemophilia B. . 2023-06-28. Pubmed ID: 37445943; DOI: 10.3390/ijms241310766; PMC: PMC10341900 SXMUi001-A 2023-06-28 2023-06-28 PubMed: 37445943 DOI: 10.3390/ijms241310766Associated cell lines:
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Correia Cátia D., Ferreira Anita, Fernandes Mónica T., Silva Bárbara M., Esteves Filipa, Leitão Helena S., Bragança José, Calado Sofia M.
Human Stem Cells for Cardiac Disease Modeling and Preclinical and Clinical Applications—Are We on the Road to Success?
Correia Cátia D. et al. Human Stem Cells for Cardiac Disease Modeling and Preclinical and Clinical Applications—Are We on the Road to Success?. . 2023-06-27. DOI: 10.3390/cells12131727 UALGi001-AUALGi002-A 2023-06-27 2023-06-27 DOI: 10.3390/cells12131727Associated cell lines:
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Overeem AW, Chang YW, Moustakas I, Roelse CM, Hillenius S, Helm TV, Schrier VFV, Gonçalves MAFV, Mei H, Freund C, Chuva de Sousa Lopes SM
Efficient and scalable generation of primordial germ cells in 2D culture using basement membrane extract overlay
Overeem AW et al. Efficient and scalable generation of primordial germ cells in 2D culture using basement membrane extract overlay. . 2023-06-26. Pubmed ID: 37426764; DOI: 10.1016/j.crmeth.2023.100488; PMC: PMC10326346 WAe001-ALUMCi004-ALUMCi001-BLUMCi028-ALUMCi029-ALUMCi004-C 2023-06-26 2023-06-26 PubMed: 37426764 DOI: 10.1016/j.crmeth.2023.100488Associated cell lines:
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Guo Y, Shen M, Dong Q, Méndez-Albelo NM, Huang SX, Sirois CL, Le J, Li M, Jarzembowski ED, Schoeller KA, Stockton ME, Horner VL, Sousa AMM, Gao Y, Birth Defects Research Laboratory, Levine JE, Wang D, Chang Q, Zhao X
Elevated levels of FMRP-target MAP1B impair human and mouse neuronal development and mouse social behaviors via autophagy pathway
Guo Y et al. Elevated levels of FMRP-target MAP1B impair human and mouse neuronal development and mouse social behaviors via autophagy pathway. . 2023-06-26. Pubmed ID: 37365192; DOI: 10.1038/s41467-023-39337-0; PMC: PMC10293283 WAe009-AWAe009-A-36 2023-06-26 2023-06-26 PubMed: 37365192 DOI: 10.1038/s41467-023-39337-0Associated cell lines:
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Qiu Yue, Wang Hongyang, Fan Mingjie, Pan Huaye, Guan Jing, Jiang Yangwei, Jia Zexiao, Wu Kaiwen, Zhou Hui, Zhuang Qianqian, Lei Zhaoying, Ding Xue, Cai Huajian, Dong Yufei, Yan Lei, Lin Aifu, Fu Yong, Zhang Dong, Yan Qingfeng, Wang Qiuju
Impaired AIF-CHCHD4 interaction and mitochondrial calcium overload contribute to auditory neuropathy spectrum disorder in patient-iPSC-derived neurons with AIFM1 variant
Qiu Yue et al. Impaired AIF-CHCHD4 interaction and mitochondrial calcium overload contribute to auditory neuropathy spectrum disorder in patient-iPSC-derived neurons with AIFM1 variant. . 2023-06-26. DOI: 10.1038/s41419-023-05899-6 CPGHi003-AUMi040-A 2023-06-26 2023-06-26 DOI: 10.1038/s41419-023-05899-6Associated cell lines:
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Chohra I, Giri S, Malgrange B
Generation of a Well-Characterized Homozygous Chromodomain-Helicase-DNA-Binding Protein 4(G1003D) Mutant hESC Line Using CRISPR/eCas9 (ULIEGEe001-A-1)
Chohra I et al. Generation of a Well-Characterized Homozygous Chromodomain-Helicase-DNA-Binding Protein 4(G1003D) Mutant hESC Line Using CRISPR/eCas9 (ULIEGEe001-A-1). . 2023-06-23. Pubmed ID: 37445725; DOI: 10.3390/ijms241310543; PMC: PMC10342000 WAe009-AWAe009-A-16WAe025-AWAe025-A-1 2023-06-23 2023-06-23 PubMed: 37445725 DOI: 10.3390/ijms241310543Associated cell lines:
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Klaihmon P, Kang X, Issaragrisil S, Luanpitpong S
Generation and Functional Characterization of Anti-CD19 Chimeric Antigen Receptor-Natural Killer Cells from Human Induced Pluripotent Stem Cells
Klaihmon P et al. Generation and Functional Characterization of Anti-CD19 Chimeric Antigen Receptor-Natural Killer Cells from Human Induced Pluripotent Stem Cells. . 2023-06-22. Pubmed ID: 37445684; DOI: 10.3390/ijms241310508; PMC: PMC10341790 MUSIi013-AMUSIi013-A-1 2023-06-22 2023-06-22 PubMed: 37445684 DOI: 10.3390/ijms241310508Associated cell lines:
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Nakhaei-Rad S, Haghighi F, Bazgir F, Dahlmann J, Busley AV, Buchholzer M, Kleemann K, Schänzer A, Borchardt A, Hahn A, Kötter S, Schanze D, Anand R, Funk F, Kronenbitter AV, Scheller J, Piekorz RP, Reichert AS, Volleth M, Wolf MJ, Cirstea IC, Gelb BD, Tartaglia M, Schmitt JP, Krüger M, Kutschka I, Cyganek L, Zenker M, Kensah G, Ahmadian MR
Molecular and cellular evidence for the impact of a hypertrophic cardiomyopathy-associated RAF1 variant on the structure and function of contractile machinery in bioartificial cardiac tissues
Nakhaei-Rad S et al. Molecular and cellular evidence for the impact of a hypertrophic cardiomyopathy-associated RAF1 variant on the structure and function of contractile machinery in bioartificial cardiac tissues. . 2023-06-21. Pubmed ID: 37344639; DOI: 10.1038/s42003-023-05013-8; PMC: PMC10284840 UMGi102-AUMGi014-CUMGi020-BUMGi102-A-1UMGi163-AUMGi164-A 2023-06-21 2023-06-21 PubMed: 37344639 DOI: 10.1038/s42003-023-05013-8 -
Li N, Edel M, Liu K, Denning C, Betts J, Neely OC, Li D, Paterson DJ
Human induced pluripotent stem cell-derived cardiac myocytes and sympathetic neurons in disease modelling
Li N et al. Human induced pluripotent stem cell-derived cardiac myocytes and sympathetic neurons in disease modelling. . 2023-06-19. Pubmed ID: 37122212; DOI: 10.1098/rstb.2022.0173; PMC: PMC10150199 UKKi007-A 2023-06-19 2023-06-19 PubMed: 37122212 DOI: 10.1098/rstb.2022.0173Associated cell lines:
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Cuevas-Ocaña S, Yang JY, Aushev M, Schlossmacher G, Bear CE, Hannan NRF, Perkins ND, Rossant J, Wong AP, Gray MA
A Cell-Based Optimised Approach for Rapid and Efficient Gene Editing of Human Pluripotent Stem Cells
Cuevas-Ocaña S et al. A Cell-Based Optimised Approach for Rapid and Efficient Gene Editing of Human Pluripotent Stem Cells. . 2023-06-17. Pubmed ID: 37373413; DOI: 10.3390/ijms241210266; PMC: PMC10299534 MSHRIe001-AMHHi006-AMHHi006-A-4 2023-06-17 2023-06-17 PubMed: 37373413 DOI: 10.3390/ijms241210266Associated cell lines:
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Shabani K, Pigeon J, Benaissa Touil Zariouh M, Liu T, Saffarian A, Komatsu J, Liu E, Danda N, Becmeur-Lefebvre M, Limame R, Bohl D, Parras C, Hassan BA
The temporal balance between self-renewal and differentiation of human neural stem cells requires the amyloid precursor protein
Shabani K et al. The temporal balance between self-renewal and differentiation of human neural stem cells requires the amyloid precursor protein. . 2023-06-16. Pubmed ID: 37327344; DOI: 10.1126/sciadv.add5002; PMC: PMC10275593 WTSIi002-AWTSIi008-A 2023-06-16 2023-06-16 PubMed: 37327344 DOI: 10.1126/sciadv.add5002Associated cell lines:
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Siles L, Ruiz-Nogales S, Navinés-Ferrer A, Méndez-Vendrell P, Pomares E
Efficient correction of ABCA4 variants by CRISPR-Cas9 in hiPSCs derived from Stargardt disease patients
Siles L et al. Efficient correction of ABCA4 variants by CRISPR-Cas9 in hiPSCs derived from Stargardt disease patients. . 2023-06-13. Pubmed ID: 36969552; DOI: 10.1016/j.omtn.2023.02.032; PMC: PMC10034418 FRIMOi003-AFRIMOi004-A 2023-06-13 2023-06-13 PubMed: 36969552 DOI: 10.1016/j.omtn.2023.02.032Associated cell lines:
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Boon N, Lu X, Andriessen CA, Moustakas I, Buck TM, Freund C, Arendzen CH, Böhringer S, Boon CJF, Mei H, Wijnholds J
AAV-mediated gene augmentation therapy of CRB1 patient-derived retinal organoids restores the histological and transcriptional retinal phenotype
Boon N et al. AAV-mediated gene augmentation therapy of CRB1 patient-derived retinal organoids restores the histological and transcriptional retinal phenotype. . 2023-06-13. Pubmed ID: 37315526; DOI: 10.1016/j.stemcr.2023.05.008; PMC: PMC10277829 LUMCi055-ALUMCi056-ALUMCi054-A-2LUMCi056-A-1 2023-06-13 2023-06-13 PubMed: 37315526 DOI: 10.1016/j.stemcr.2023.05.008Associated cell lines:
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Rudraraju R, Gartner MJ, Neil JA, Stout ES, Chen J, Needham EJ, See M, Mackenzie-Kludas C, Yang Lee LY, Wang M, Pointer H, Karavendzas K, Abu-Bonsrah D, Drew D, Yang Sun YB, Tan JP, Sun G, Salavaty A, Charitakis N, Nim HT, Currie PD, Tham WH, Porrello E, Polo JM, Humphrey SJ, Ramialison M, Elliott DA, Subbarao K
Parallel use of human stem cell lung and heart models provide insights for SARS-CoV-2 treatment
Rudraraju R et al. Parallel use of human stem cell lung and heart models provide insights for SARS-CoV-2 treatment. . 2023-06-13. Pubmed ID: 37315523; DOI: 10.1016/j.stemcr.2023.05.007; PMC: PMC10262339 MCRIi010-A 2023-06-13 2023-06-13 PubMed: 37315523 DOI: 10.1016/j.stemcr.2023.05.007Associated cell lines:
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Park Hye Jung, Choi Yong Jun, Park Chul Hwan, Kim Tae Hoon, Lee Sung Soo, Moon Duk Hwan, Lee Kyung-A, Lee Sang Eun, Park Moo Suk, Kim Song Yee, Chang Yoon Soo, Lee Seok Jeong, Jung Ji Ye, Lee Ji-Ho, Lee Su Hwan, Kim Taehee, Kim Sung-Ryeol, Kim Kangjoon, Byun Min Kwang
Outstanding Characteristics of Birt–Hogg–Dube Syndrome in Korea
Park Hye Jung et al. Outstanding Characteristics of Birt–Hogg–Dube Syndrome in Korea. . 2023-06-13. DOI: 10.3390/diagnostics13122047 CMCi009-A 2023-06-13 2023-06-13 DOI: 10.3390/diagnostics13122047Associated cell lines:
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Xiang-Tischhauser Li, Bette Michael, Rusche Johanna R., Roth Katrin, Kasahara Norio, Stuck Boris A., Bakowsky Udo, Wartenberg Maria, Sauer Heinrich, Geisthoff Urban W., Mandic Robert
Generation of a Syngeneic Heterozygous ACVRL1(wt/mut) Knockout iPS Cell Line for the In Vitro Study of HHT2-Associated Angiogenesis
Xiang-Tischhauser Li et al. Generation of a Syngeneic Heterozygous ACVRL1(wt/mut) Knockout iPS Cell Line for the In Vitro Study of HHT2-Associated Angiogenesis. . 2023-06-10. DOI: 10.3390/cells12121600 KMUGMCi001-A 2023-06-10 2023-06-10 DOI: 10.3390/cells12121600Associated cell lines:
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Rájová J, Davidsson M, Avallone M, Hartnor M, Aldrin-Kirk P, Cardoso T, Nolbrant S, Mollbrink A, Storm P, Heuer A, Parmar M, Björklund T
Deconvolution of spatial sequencing provides accurate characterization of hESC-derived DA transplants in vivo
Rájová J et al. Deconvolution of spatial sequencing provides accurate characterization of hESC-derived DA transplants in vivo. . 2023-06-08. Pubmed ID: 37251982; DOI: 10.1016/j.omtm.2023.04.008; PMC: PMC10209706 RCe021-A 2023-06-08 2023-06-08 PubMed: 37251982 DOI: 10.1016/j.omtm.2023.04.008Associated cell lines:
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Banerjee R, Raj A, Potdar C, Pal PK, Yadav R, Kamble N, Holla V, Datta I
Astrocytes Differentiated from LRRK2-I1371V Parkinson's-Disease-Induced Pluripotent Stem Cells Exhibit Similar Yield but Cell-Intrinsic Dysfunction in Glutamate Uptake and Metabolism, ATP Generation, and Nrf2-Mediated Glutathione Machinery
Banerjee R et al. Astrocytes Differentiated from LRRK2-I1371V Parkinson's-Disease-Induced Pluripotent Stem Cells Exhibit Similar Yield but Cell-Intrinsic Dysfunction in Glutamate Uptake and Metabolism, ATP Generation, and Nrf2-Mediated Glutathione Machinery. . 2023-06-08. Pubmed ID: 37371062; DOI: 10.3390/cells12121592; PMC: PMC10297190 NIMHi001-ANIMHi004-ANIMHi005-ANIMHi006-A 2023-06-08 2023-06-08 PubMed: 37371062 DOI: 10.3390/cells12121592Associated cell lines:
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Rosner Margit, Horer Stefanie, Feichtinger Michael, Hengstschläger Markus
Multipotent fetal stem cells in reproductive biology research
Rosner Margit et al. Multipotent fetal stem cells in reproductive biology research. . 2023-06-07. DOI: 10.1186/s13287-023-03379-4 VRISGi001-A 2023-06-07 2023-06-07 DOI: 10.1186/s13287-023-03379-4Associated cell lines:
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Cuesta-Gomez N, Verhoeff K, Dadheech N, Dang T, Jasra IT, de Leon MB, Pawlick R, Marfil-Garza B, Anwar P, Razavy H, Zapata-Morin PA, Jickling G, Thiesen A, O'Gorman D, Kallos MS, Shapiro AMJ
Suspension culture improves iPSC expansion and pluripotency phenotype
Cuesta-Gomez N et al. Suspension culture improves iPSC expansion and pluripotency phenotype. . 2023-06-06. Pubmed ID: 37280707; DOI: 10.1186/s13287-023-03382-9; PMC: PMC10245469 MHHi001-AMHHi006-AMHHi008-A 2023-06-06 2023-06-06 PubMed: 37280707 DOI: 10.1186/s13287-023-03382-9 -
Zaghi M, Banfi F, Massimino L, Volpin M, Bellini E, Brusco S, Merelli I, Barone C, Bruni M, Bossini L, Lamparelli LA, Pintado L, D'Aliberti D, Spinelli S, Mologni L, Colasante G, Ungaro F, Cioni JM, Azzoni E, Piazza R, Montini E, Broccoli V, Sessa A
Balanced SET levels favor the correct enhancer repertoire during cell fate acquisition
Zaghi M et al. Balanced SET levels favor the correct enhancer repertoire during cell fate acquisition. . 2023-06-03. Pubmed ID: 37270547; DOI: 10.1038/s41467-023-39043-x; PMC: PMC10239470 OSRi009-AOSRi009-A-1OSRi010-AOSRi010-A-1 2023-06-03 2023-06-03 PubMed: 37270547 DOI: 10.1038/s41467-023-39043-xAssociated cell lines:
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Banerjee R, Raj A, Potdar C, Kumar Pal P, Yadav R, Kamble N, Holla V, Datta I.
Astrocytes Differentiated from LRRK2-I1371V Parkinson’s-Disease-Induced Pluripotent Stem Cells Exhibit Similar Yield but Cell-Intrinsic Dysfunction in Glutamate Uptake and Metabolism, ATP Generation, and Nrf2-Mediated Glutathione Machinery
Banerjee R et al. Astrocytes Differentiated from LRRK2-I1371V Parkinson’s-Disease-Induced Pluripotent Stem Cells Exhibit Similar Yield but Cell-Intrinsic Dysfunction in Glutamate Uptake and Metabolism, ATP Generation, and Nrf2-Mediated Glutathione Machinery. . 2023-06-01. NIMHi001-A 2023-06-01 2023-06-01Associated cell lines:
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Wong Poh Kuan, Mohamad Zamberi Nurul Nadia, Syafruddin Saiful Effendi, Cheah Fook Choe, Azmi Norazrina, Law Jia Xian, Chua Eng Wee
The Promises and Pitfalls of CRISPR-Mediated Base Editing in Stem Cells
Wong Poh Kuan et al. The Promises and Pitfalls of CRISPR-Mediated Base Editing in Stem Cells. . 2023-06-01. DOI: 10.1089/crispr.2023.0013 UMi028-AUMi028-A-2DHMi005-ADHMi005-A-1 2023-06-01 2023-06-01 DOI: 10.1089/crispr.2023.0013Associated cell lines:
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Braam MJS, Zhao J, Liang S, Ida S, Kloostra NK, Iworima DG, Tang M, Baker RK, Quiskamp N, Piret JM, Kieffer TJ
Protocol development to further differentiate and transition stem cell-derived pancreatic progenitors from a monolayer into endocrine cells in suspension culture
Braam MJS et al. Protocol development to further differentiate and transition stem cell-derived pancreatic progenitors from a monolayer into endocrine cells in suspension culture. . 2023-06-01. Pubmed ID: 37264038; DOI: 10.1038/s41598-023-35716-1; PMC: PMC10235054 SCTi002-A 2023-06-01 2023-06-01 PubMed: 37264038 DOI: 10.1038/s41598-023-35716-1Associated cell lines:
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Akter M, Cui H, Abir Hosain M, Ding B
Generation of two induced pluripotent stem cell lines with heterozygous and homozygous amyotrophic lateral sclerosis-causing mutation R521G (c.1561C > G) in FUS gene
Akter M et al. Generation of two induced pluripotent stem cell lines with heterozygous and homozygous amyotrophic lateral sclerosis-causing mutation R521G (c.1561C > G) in FUS gene. . 2023-06-00. Pubmed ID: 36965406; DOI: 10.1016/j.scr.2023.103078; PMC: PMC10353567 UCSFi001-AUCSFi001-A-72UCSFi001-A-73 2023-06-00 2023-06-00 PubMed: 36965406 DOI: 10.1016/j.scr.2023.103078Associated cell lines:
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Luo Xian, Yang Kaiming, Jiang Meiling, Chen Tao, Chi Yue, Ma Bingxiu, Lai Liangxue, Zou Qingjian
Generation of a homozygous GRIN2A gene knockout human embryonic stem cell line using CRISPR/Cas9 system
Luo Xian et al. Generation of a homozygous GRIN2A gene knockout human embryonic stem cell line using CRISPR/Cas9 system. . 2023-06-00. DOI: 10.1016/j.scr.2023.103121 GZHMCe003-A 2023-06-00 2023-06-00 DOI: 10.1016/j.scr.2023.103121Associated cell lines:
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Kong X, Belbachir N, Zeng W, Yan CD, Navada S, Perez MV, Wu JC
Generation of two induced pluripotent stem cell lines from catecholaminergic polymorphic ventricular tachycardia patients carrying RYR2 mutations
Kong X et al. Generation of two induced pluripotent stem cell lines from catecholaminergic polymorphic ventricular tachycardia patients carrying RYR2 mutations. . 2023-06-00. Pubmed ID: 37210947; DOI: 10.1016/j.scr.2023.103111; PMC: PMC11059235 SCVIi077-ASCVIi078-A 2023-06-00 2023-06-00 PubMed: 37210947 DOI: 10.1016/j.scr.2023.103111Associated cell lines:
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Busley AV, Cyganek L
Generation of a genetically-modified induced pluripotent stem cell line harboring a Noonan syndrome-associated gene variant MRAS p.G23V
Busley AV et al. Generation of a genetically-modified induced pluripotent stem cell line harboring a Noonan syndrome-associated gene variant MRAS p.G23V. . 2023-06-00. Pubmed ID: 37141804; DOI: 10.1016/j.scr.2023.103108 UMGi014-CUMGi014-C-17 2023-06-00 2023-06-00 PubMed: 37141804 DOI: 10.1016/j.scr.2023.103108Associated cell lines:
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Gao Y, Cheng Y, Wen J, Xiao D, Xu J, Cai C, Hu J
Efficient generation of induced pluripotent stem cell lines from peripheral blood mononuclear cells
Gao Y et al. Efficient generation of induced pluripotent stem cell lines from peripheral blood mononuclear cells. . 2023-06-00. Pubmed ID: 37099933; DOI: 10.1016/j.scr.2023.103088 ZZUSAHi002-ASZBKi001-ASZBKi001-BSZBKi002-ASZBKi002-B 2023-06-00 2023-06-00 PubMed: 37099933 DOI: 10.1016/j.scr.2023.103088Associated cell lines:
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Alonso-Carriazo Fernández A, Ashley-Norman P, Butt Z, Moosajee M, Carr AF
Establishment and characterization of an iPSC line (UCLi023-A) derived from a Late-Onset Retinal Degeneration patient carrying a founder mutation in C1QTNF5
Alonso-Carriazo Fernández A et al. Establishment and characterization of an iPSC line (UCLi023-A) derived from a Late-Onset Retinal Degeneration patient carrying a founder mutation in C1QTNF5. . 2023-06-00. Pubmed ID: 37207468; DOI: 10.1016/j.scr.2023.103110 UCLi023-A 2023-06-00 2023-06-00 PubMed: 37207468 DOI: 10.1016/j.scr.2023.103110Associated cell lines:
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Chan YH, Tsai CY, Ho CH, Lu YC, Lin PH, Chen TC, Chen YT, Huang CY, Liu TC, Hsu CJ, Wu CC
Generation of induced pluripotent stem cells (IBMSi027-A) from a patient with hearing loss carrying WFS1 c.2051C > T (p.Ala684Val) variant
Chan YH et al. Generation of induced pluripotent stem cells (IBMSi027-A) from a patient with hearing loss carrying WFS1 c.2051C > T (p.Ala684Val) variant. . 2023-06-00. Pubmed ID: 36933359; DOI: 10.1016/j.scr.2023.103068 IBMSi027-A 2023-06-00 2023-06-00 PubMed: 36933359 DOI: 10.1016/j.scr.2023.103068Associated cell lines:
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Morimoto Satoru, Takahashi Shinichi, Ito Daisuke, Daté Yugaku, Okada Kensuke, Kato Chris, Nakamura Shiho, Ozawa Fumiko, Chyi Chai Muh, Nishiyama Ayumi, Suzuki Naoki, Fujimori Koki, Kondo Tosho, Takao Masaki, Hirai Miwa, Kabe Yasuaki, Suematsu Makoto, Jinzaki Masahiro, Aoki Masashi, Fujiki Yuto, Sato Yasunori, Suzuki Norihiro, Nakahara Jin, Okano Hideyuki
Phase 1/2a clinical trial in ALS with ropinirole, a drug candidate identified by iPSC drug discovery
Morimoto Satoru et al. Phase 1/2a clinical trial in ALS with ropinirole, a drug candidate identified by iPSC drug discovery. . 2023-06-00. DOI: 10.1016/j.stem.2023.04.017 KEIOi001-A 2023-06-00 2023-06-00 DOI: 10.1016/j.stem.2023.04.017Associated cell lines:
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Busley AV, Kleinsorge M, Cyganek L
Generation of a genetically-modified induced pluripotent stem cell line harboring an oncogenic gene variant KRAS p.G12V
Busley AV et al. Generation of a genetically-modified induced pluripotent stem cell line harboring an oncogenic gene variant KRAS p.G12V. . 2023-06-00. Pubmed ID: 37121193; DOI: 10.1016/j.scr.2023.103105 UMGi014-CUMGi014-C-2 2023-06-00 2023-06-00 PubMed: 37121193 DOI: 10.1016/j.scr.2023.103105Associated cell lines:
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Huang J, Wang Y, Zhao J, Deng Y, Wei W
Establishment of an induced pluripotent stem cell (SIAISi016-A) line from a 62-years old Chinese Han patient with Alzheimer's disease
Huang J et al. Establishment of an induced pluripotent stem cell (SIAISi016-A) line from a 62-years old Chinese Han patient with Alzheimer's disease. . 2023-06-00. Pubmed ID: 37148820; DOI: 10.1016/j.scr.2023.103091 SIAISi016-A 2023-06-00 2023-06-00 PubMed: 37148820 DOI: 10.1016/j.scr.2023.103091Associated cell lines:
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Salvarani N, Peretto G, Silvia C, Villatore A, Thairi C, Santoni A, Galli C, Carrera P, Sala S, Benedetti S, Di Pasquale E, Di Resta C
Functional Characterisation of the Rare SCN5A p.E1225K Variant, Segregating in a Brugada Syndrome Familial Case, in Human Cardiomyocytes from Pluripotent Stem Cells
Salvarani N et al. Functional Characterisation of the Rare SCN5A p.E1225K Variant, Segregating in a Brugada Syndrome Familial Case, in Human Cardiomyocytes from Pluripotent Stem Cells. . 2023-05-31. Pubmed ID: 37298497; DOI: 10.3390/ijms24119548; PMC: PMC10253753 RUESe002-A 2023-05-31 2023-05-31 PubMed: 37298497 DOI: 10.3390/ijms24119548Associated cell lines:
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Batool L, Raab C, Beez CM, Kurtz A, Gollasch M, Rossbach B
Generation of human induced pluripotent stem cell line (BCRTi007-A) from urinary cells of a patient with autosomal dominant polycystic kidney disease
Batool L et al. Generation of human induced pluripotent stem cell line (BCRTi007-A) from urinary cells of a patient with autosomal dominant polycystic kidney disease. . 2023-06-00. Pubmed ID: 36947994; DOI: 10.1016/j.scr.2023.103071 BCRTi007-A 2023-06-00 2023-06-00 PubMed: 36947994 DOI: 10.1016/j.scr.2023.103071Associated cell lines:
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Schmitz AS, Korneck M, Raju J, Lamsfus-Calle A, Daniel-Moreno A, Antony JS, Mezger M, Schöls L, Hauser S, Hayer SN
Generation of a heterozygous and a homozygous CSF1R knockout line from iPSC using CRISPR/Cas9
Schmitz AS et al. Generation of a heterozygous and a homozygous CSF1R knockout line from iPSC using CRISPR/Cas9. . 2023-06-00. Pubmed ID: 36947995; DOI: 10.1016/j.scr.2023.103066 HIHCNi003-AHIHCNi007-AHIHCNi007-A-1HIHCNi007-A-2 2023-06-00 2023-06-00 PubMed: 36947995 DOI: 10.1016/j.scr.2023.103066Associated cell lines:
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Merkert S, Haase A, Dahlmann J, Göhring G, Waqas FH, Pessler F, Martin U, Olmer R
Generation of two human NRF2 knockout iPSC clones using CRISPR/Cas9 editing
Merkert S et al. Generation of two human NRF2 knockout iPSC clones using CRISPR/Cas9 editing. . 2023-06-00. Pubmed ID: 37104932; DOI: 10.1016/j.scr.2023.103090 MHHi001-AMHHi001-A-6MHHi001-A-7 2023-06-00 2023-06-00 PubMed: 37104932 DOI: 10.1016/j.scr.2023.103090Associated cell lines:
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Batool L, Raab C, Beez CM, Hariharan K, Kurtz A, Gollasch M, Rossbach B
Generation of human induced pluripotent stem cell line (BCRTi006-A) from a patient with focal segmental glomerulosclerosis disease
Batool L et al. Generation of human induced pluripotent stem cell line (BCRTi006-A) from a patient with focal segmental glomerulosclerosis disease. . 2023-06-00. Pubmed ID: 36958215; DOI: 10.1016/j.scr.2023.103070 BCRTi006-A 2023-06-00 2023-06-00 PubMed: 36958215 DOI: 10.1016/j.scr.2023.103070Associated cell lines:
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Kozhushko N, Beilina A, Cookson MR
Generation of gene-corrected isogenic controls from Parkinson's disease patient iPSC lines carrying the pathogenic SNCA p.A53T variant
Kozhushko N et al. Generation of gene-corrected isogenic controls from Parkinson's disease patient iPSC lines carrying the pathogenic SNCA p.A53T variant. . 2023-06-00. Pubmed ID: 37229975; DOI: 10.1016/j.scr.2023.103125; PMC: PMC10411637 NIAi002-ANIAi003-ANIAi002-A-1NIAi002-A-2NIAi002-A-3NIAi003-A-1NIAi003-A-2NIAi003-A-3 2023-06-00 2023-06-00 PubMed: 37229975 DOI: 10.1016/j.scr.2023.103125Associated cell lines:
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Stewart R, Gadoud C, Krawczyk J, McInerney V, O'Brien T, Shen S, Allen NM
Generation of three induced pluripotent stem cell lines from a patient with KCNQ2 developmental and epileptic encephalopathy as a result of the pathogenic variant c.638C > T; p.Arg213Gln (NUIGi063-A, NUIGi063-B, NUIGi063-C) and 3 healthy controls (NUIGi064-A, NUIGi064-B, NUIGi064-C)
Stewart R et al. Generation of three induced pluripotent stem cell lines from a patient with KCNQ2 developmental and epileptic encephalopathy as a result of the pathogenic variant c.638C > T; p.Arg213Gln (NUIGi063-A, NUIGi063-B, NUIGi063-C) and 3 healthy controls (NUIGi064-A, NUIGi064-B, NUIGi064-C). . 2023-06-00. Pubmed ID: 37071954; DOI: 10.1016/j.scr.2023.103093 NUIGi063-ANUIGi063-BNUIGi063-CNUIGi064-ANUIGi064-BNUIGi064-C 2023-06-00 2023-06-00 PubMed: 37071954 DOI: 10.1016/j.scr.2023.103093Associated cell lines:
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Almad AA, Garcia L, Takanohashi A, Gagne A, Yang W, Ann McGuire J, French D, Vanderver A
Generation of three induced Pluripotent Stem Cell lines from individuals with Hypomyelination with Atrophy of Basal Ganglia and Cerebellum caused by a c.745G>A (p.D249N) autosomal dominant mutation in TUBB4A
Almad AA et al. Generation of three induced Pluripotent Stem Cell lines from individuals with Hypomyelination with Atrophy of Basal Ganglia and Cerebellum caused by a c.745G>A (p.D249N) autosomal dominant mutation in TUBB4A. . 2023-06-00. Pubmed ID: 37003180; DOI: 10.1016/j.scr.2023.103083 CHOPi005-ACHOPi006-ACHOPi007-A 2023-06-00 2023-06-00 PubMed: 37003180 DOI: 10.1016/j.scr.2023.103083Associated cell lines:
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Nievas M, Romorini L, Isaja L, Clas GS, Rodríguez-Varela S, Mucci S, Itzcovich T, de Ambrosi B, Scassa ME, Sevlever GE, Surace EI, Marazita MC
Generation of a human induced pluripotent stem cell line (INEUi001-A) from an amyotrophic lateral sclerosis/frontotemporal dementia patient with a C9ORF72 G4C2 genotype of <2 (GGGGCCG) and 10 repeats
Nievas M et al. Generation of a human induced pluripotent stem cell line (INEUi001-A) from an amyotrophic lateral sclerosis/frontotemporal dementia patient with a C9ORF72 G4C2 genotype of <2 (GGGGCCG) and 10 repeats. . 2023-06-00. Pubmed ID: 36963214; DOI: 10.1016/j.scr.2023.103076 INEUi001-A 2023-06-00 2023-06-00 PubMed: 36963214 DOI: 10.1016/j.scr.2023.103076Associated cell lines:
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Yin T, Wu B, Peng T, Liao Y, Jiao S, Wang H
Generation of a human induced pluripotent stem cell line (FDCHi010-A) from a patient with Xia-Gibbs syndrome carrying AHDC1 mutation (c.2062C > T)
Yin T et al. Generation of a human induced pluripotent stem cell line (FDCHi010-A) from a patient with Xia-Gibbs syndrome carrying AHDC1 mutation (c.2062C > T). . 2023-06-00. Pubmed ID: 37216737; DOI: 10.1016/j.scr.2023.103118 FDCHi010-A 2023-06-00 2023-06-00 PubMed: 37216737 DOI: 10.1016/j.scr.2023.103118Associated cell lines:
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Yde Ohki CM, Walter NM, Rickli M, Van Puyenbroeck P, Döring C, Hoffmann P, Herms S, Maria Werling A, Walitza S, Grünblatt E
Generation of induced pluripotent stem cells from two ADHD patients and two healthy controls
Yde Ohki CM et al. Generation of induced pluripotent stem cells from two ADHD patients and two healthy controls. . 2023-06-00. Pubmed ID: 37004448; DOI: 10.1016/j.scr.2023.103084 TMPi008-BTMPi010-ATMPi010-BTMPi011-ATMPi011-BTMPi012-ATMPi012-B 2023-06-00 2023-06-00 PubMed: 37004448 DOI: 10.1016/j.scr.2023.103084 -
De Kinderen P, Rabaut L, Perik MHAM, Peeters S, Ponsaerts P, Loeys B, Mortier G, Meester JAN, Verstraeten A
IPSC reprogramming of two patients with spondyloepiphyseal dysplasia congenita (SEDC)
De Kinderen P et al. IPSC reprogramming of two patients with spondyloepiphyseal dysplasia congenita (SEDC). . 2023-06-00. Pubmed ID: 36966641; DOI: 10.1016/j.scr.2023.103080; PMC: PMC10240565 BBANTWi006-ABBANTWi007-ACMGANTi006-ACMGANTi007-A 2023-06-00 2023-06-00 PubMed: 36966641 DOI: 10.1016/j.scr.2023.103080Associated cell lines:
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Kim AH, Lee HM, Kim HS, Jung J, Seol H, Choi E, Lee S, Min Choi Y, Jun JK, Kim HS, Jang J
Establishment of TUBB3-mCherry knock-in human pluripotent stem cell line using CRISPR/Cas9 (SNUe003-A-4)
Kim AH et al. Establishment of TUBB3-mCherry knock-in human pluripotent stem cell line using CRISPR/Cas9 (SNUe003-A-4). . 2023-06-00. Pubmed ID: 36913849; DOI: 10.1016/j.scr.2023.103064 SNUe003-ASNUe003-A-4 2023-06-00 2023-06-00 PubMed: 36913849 DOI: 10.1016/j.scr.2023.103064Associated cell lines:
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Ai D, Yang X, Li X, Liu N, Xie X, Liu Y, Song W
Generation of an induced pluripotent stem cell line SDPHi002-A from a patient with lung cancer
Ai D et al. Generation of an induced pluripotent stem cell line SDPHi002-A from a patient with lung cancer. . 2023-06-00. Pubmed ID: 37104933; DOI: 10.1016/j.scr.2023.103096 SDQLCHi032-ASDQLCHi040-ASDPHi002-A 2023-06-00 2023-06-00 PubMed: 37104933 DOI: 10.1016/j.scr.2023.103096Associated cell lines:
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Chemla A, Arena G, Saraiva C, Berenguer-Escuder C, Grossmann D, Grünewald A, Klein C, Seibler P, Schwamborn JC, Krüger R
Generation of two induced pluripotent stem cell lines and the corresponding isogenic controls from Parkinson's disease patients carrying the heterozygous mutations c.1290A > G (p.T351A) or c.2067A > G (p.T610A) in the RHOT1 gene encoding Miro1
Chemla A et al. Generation of two induced pluripotent stem cell lines and the corresponding isogenic controls from Parkinson's disease patients carrying the heterozygous mutations c.1290A > G (p.T351A) or c.2067A > G (p.T610A) in the RHOT1 gene encoding Miro1. . 2023-06-00. Pubmed ID: 37003181; DOI: 10.1016/j.scr.2023.103085; PMC: PMC10240566 LCSBi011-ALCSBi011-A-1LCSBi012-ALCSBi012-A-1 2023-06-00 2023-06-00 PubMed: 37003181 DOI: 10.1016/j.scr.2023.103085Associated cell lines:
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Li P, Wang C, Wang J, Tan J, Liu Y, Lin Y
Generation of an induced pluripotent stem cell lines NSHDMUi001-A from patients with type 2 diabetes
Li P et al. Generation of an induced pluripotent stem cell lines NSHDMUi001-A from patients with type 2 diabetes. . 2023-06-00. Pubmed ID: 37028179; DOI: 10.1016/j.scr.2023.103087 NSHDMUi001-A 2023-06-00 2023-06-00 PubMed: 37028179 DOI: 10.1016/j.scr.2023.103087Associated cell lines:
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Wu X, Wang X
Generation of a TBX20-knockout human embryonic stem line by CRISPR/Cas9 system
Wu X et al. Generation of a TBX20-knockout human embryonic stem line by CRISPR/Cas9 system. . 2023-06-00. Pubmed ID: 36963213; DOI: 10.1016/j.scr.2023.103082 WAe009-AWAe009-A-36WAe009-A-84 2023-06-00 2023-06-00 PubMed: 36963213 DOI: 10.1016/j.scr.2023.103082Associated cell lines:
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Lebedeva O, Poberezhniy D, Novosadova E, Gerasimova T, Novosadova L, Arsenyeva E, Stepanenko E, Shimchenko D, Volovikov E, Anufrieva K, Illarioshkin S, Lagarkova M, Grivennikov I, Tarantul V, Nenasheva V
Overexpression of Parkin in the Neuronal Progenitor Cells from a Patient with Parkinson's Disease Shifts the Transcriptome Towards the Normal State
Lebedeva O et al. Overexpression of Parkin in the Neuronal Progenitor Cells from a Patient with Parkinson's Disease Shifts the Transcriptome Towards the Normal State. . 2023-06-00. Pubmed ID: 36884134; DOI: 10.1007/s12035-023-03293-z RCPCMi004-A 2023-06-00 2023-06-00 PubMed: 36884134 DOI: 10.1007/s12035-023-03293-zAssociated cell lines:
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Patlolla N, Ponnachan P, Jamora C, Abbey D
Generation of control human iPSC line INSTEMi001-A from PBMCs of a healthy Indian donor
Patlolla N et al. Generation of control human iPSC line INSTEMi001-A from PBMCs of a healthy Indian donor. . 2023-06-00. Pubmed ID: 37236122; DOI: 10.1016/j.scr.2023.103112 INSTEMi001-A 2023-06-00 2023-06-00 PubMed: 37236122 DOI: 10.1016/j.scr.2023.103112Associated cell lines:
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Jung M, Hartmann C, Ehrhardt T, Peter LM, Abid CL, Harwardt B, Hirschfeld J, Claus C, Haferkamp U, Pless O, Nastainczyk-Wulf M, Kehlen A, Schlote D, Schroder IS, Rujescu D
Generation of a set of induced pluripotent stem cell lines from two Alzheimer disease patients carrying APOE4 (MLUi007-J; MLUi008-A) and healthy old donors carrying APOE3 (MLUi009-A; MLUi010-B) to study APOE in aging and disease
Jung M et al. Generation of a set of induced pluripotent stem cell lines from two Alzheimer disease patients carrying APOE4 (MLUi007-J; MLUi008-A) and healthy old donors carrying APOE3 (MLUi009-A; MLUi010-B) to study APOE in aging and disease. . 2023-06-00. Pubmed ID: 37001364; DOI: 10.1016/j.scr.2023.103072 MLUi008-AMLUi009-AMLUi007-JMLUi008-BMLUi010-B 2023-06-00 2023-06-00 PubMed: 37001364 DOI: 10.1016/j.scr.2023.103072 -
Yang Xianguang, Zhang Baohong
A review on CRISPR/Cas: a versatile tool for cancer screening, diagnosis, and clinic treatment
Yang Xianguang et al. A review on CRISPR/Cas: a versatile tool for cancer screening, diagnosis, and clinic treatment. . 2023-06-00. DOI: 10.1007/s10142-023-01117-w ZSSYe001-A 2023-06-00 2023-06-00 DOI: 10.1007/s10142-023-01117-wAssociated cell lines:
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Even-Zohar N, Metin-Armagan D, Ben-Shlomo A, Sareen D, Melmed S
Generation of isogenic and homozygous MEN1 mutant cell lines from patient-derived iPSCs using CRISPR/Cas9
Even-Zohar N et al. Generation of isogenic and homozygous MEN1 mutant cell lines from patient-derived iPSCs using CRISPR/Cas9. . 2023-06-00. Pubmed ID: 37209468; DOI: 10.1016/j.scr.2023.103124; PMC: PMC10882434 CSMCi001-ACSMCi001-A-1CSMCi001-A-2 2023-06-00 2023-06-00 PubMed: 37209468 DOI: 10.1016/j.scr.2023.103124Associated cell lines:
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Wang X, Sun J, Fu C, Liu C
Generation of a PPP1CA knockout human pluripotent stem cell line via CRISPR/Cas9
Wang X et al. Generation of a PPP1CA knockout human pluripotent stem cell line via CRISPR/Cas9. . 2023-06-00. Pubmed ID: 36965407; DOI: 10.1016/j.scr.2023.103077 WAe009-AWAe009-A-36WAe009-A-B 2023-06-00 2023-06-00 PubMed: 36965407 DOI: 10.1016/j.scr.2023.103077Associated cell lines:
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Sun R, Cui Y, Liu Z, Guo J, Zhang X, Zhu P, Sha J, Yang X, Yuan Y
A prime editor efficiently repaired human induced pluripotent stem cells with AR gene mutation (c.2710G > A; p. V904M)
Sun R et al. A prime editor efficiently repaired human induced pluripotent stem cells with AR gene mutation (c.2710G > A; p. V904M). . 2023-06-00. Pubmed ID: 37148822; DOI: 10.1016/j.scr.2023.103102 SKLRMi001-ASKLRMi001-A-1 2023-06-00 2023-06-00 PubMed: 37148822 DOI: 10.1016/j.scr.2023.103102Associated cell lines:
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Jo S, Kim JW, Noh H, Kim H, Kim JH, Park HJ
Generation of a PDGFRB-mCherry knock-in reporter human induced pluripotent stem cell line (KITi001-A-1), using CRISPR/Cas9 nuclease
Jo S et al. Generation of a PDGFRB-mCherry knock-in reporter human induced pluripotent stem cell line (KITi001-A-1), using CRISPR/Cas9 nuclease. . 2023-06-00. Pubmed ID: 37001365; DOI: 10.1016/j.scr.2023.103081 KITi001-AKITi001-A-1 2023-06-00 2023-06-00 PubMed: 37001365 DOI: 10.1016/j.scr.2023.103081Associated cell lines:
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Christensen C, Heckman P, Rha A, Kan SH, Harb J, Wang R
Generation of two induced pluripotent stem cell lines (CHOCi002-A and CHOCi003-A) from Pompe disease patients with compound heterozygous mutations in the GAA gene
Christensen C et al. Generation of two induced pluripotent stem cell lines (CHOCi002-A and CHOCi003-A) from Pompe disease patients with compound heterozygous mutations in the GAA gene. . 2023-06-00. Pubmed ID: 37167752; DOI: 10.1016/j.scr.2023.103117; PMC: PMC10281086 TRNDi007-BCHOCi002-ACHOCi003-A 2023-06-00 2023-06-00 PubMed: 37167752 DOI: 10.1016/j.scr.2023.103117Associated cell lines:
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Zhang C, Wang D, Wang Y, Sun P, Zhao D, Zhao X, Zhao Y, Liu F, Xu J, Yan C
Generation of an induced pluripotent stem cell (iPSC) line (INNDSUi002-A) from a patient with riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency
Zhang C et al. Generation of an induced pluripotent stem cell (iPSC) line (INNDSUi002-A) from a patient with riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency. . 2023-06-00. Pubmed ID: 37019029; DOI: 10.1016/j.scr.2023.103067 INNDSUi002-A 2023-06-00 2023-06-00 PubMed: 37019029 DOI: 10.1016/j.scr.2023.103067Associated cell lines:
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Schuurmans IME, Wu KM, van Karnebeek CDM, Nadif Kasri N, Garanto A
Generation of an induced pluripotent stem cell line carrying a biallelic deletion (SCTCi019-A) in GCDH using CRISPR/Cas9
Schuurmans IME et al. Generation of an induced pluripotent stem cell line carrying a biallelic deletion (SCTCi019-A) in GCDH using CRISPR/Cas9. . 2023-06-00. Pubmed ID: 36947993; DOI: 10.1016/j.scr.2023.103069 SCTCi019-A 2023-06-00 2023-06-00 PubMed: 36947993 DOI: 10.1016/j.scr.2023.103069Associated cell lines:
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Kumar Prabodh, Paramasivam Ganesh, Prabhu Mukund A., Devasia Tom, Rajasekhar Moka
A novel FLNC variation associated with restrictive cardiomyopathy with an unusually long clinical course — A case report
Kumar Prabodh et al. A novel FLNC variation associated with restrictive cardiomyopathy with an unusually long clinical course — A case report. . 2023-06-00. DOI: 10.1016/j.genrep.2023.101769 FAMRCi009-AFAMRCi010-A 2023-06-00 2023-06-00 DOI: 10.1016/j.genrep.2023.101769Associated cell lines:
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Xi Y, Zhang H, Wang B, Song W, Liu Y
Establishment of an induced pluripotent stem cell line SDQLCHi049-A from a healthy male neonate
Xi Y et al. Establishment of an induced pluripotent stem cell line SDQLCHi049-A from a healthy male neonate. . 2023-06-00. Pubmed ID: 37075622; DOI: 10.1016/j.scr.2023.103097 SDQLCHi049-A 2023-06-00 2023-06-00 PubMed: 37075622 DOI: 10.1016/j.scr.2023.103097Associated cell lines:
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Feng Z, Yang X, Guan J, Song W, Liu Y
Establishment of an induced pluripotent stem cell line SDQLCHi048-A from a healthy boy donor
Feng Z et al. Establishment of an induced pluripotent stem cell line SDQLCHi048-A from a healthy boy donor. . 2023-06-00. Pubmed ID: 37229976; DOI: 10.1016/j.scr.2023.103115 SDQLCHi048-A 2023-06-00 2023-06-00 PubMed: 37229976 DOI: 10.1016/j.scr.2023.103115Associated cell lines:
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Vlahos K, Sourris K, Yi Kuah J, Graham A, Suter A, Howden SE, Stanley EG, Elefanty AG
Generation of iPSC lines from peripheral blood mononuclear cells from five healthy donors
Vlahos K et al. Generation of iPSC lines from peripheral blood mononuclear cells from five healthy donors. . 2023-06-00. Pubmed ID: 37150143; DOI: 10.1016/j.scr.2023.103109 MCRIi002-AMCRIi003-AMCRIi007-AMCRIi008-AMCRIi009-A 2023-06-00 2023-06-00 PubMed: 37150143 DOI: 10.1016/j.scr.2023.103109Associated cell lines:
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Fukusumi H, Togo K, Beck G, Shofuda T, Kanematsu D, Yamamoto A, Sumida M, Baba K, Mochizuki H, Kanemura Y
Human induced pluripotent stem cell line (ONHi001-A) generated from a patient with infantile neuroaxonal dystrophy having PLA2G6 c.517C > T (p.Q173X) and c.1634A > G (p.K545R) compound heterozygous mutations
Fukusumi H et al. Human induced pluripotent stem cell line (ONHi001-A) generated from a patient with infantile neuroaxonal dystrophy having PLA2G6 c.517C > T (p.Q173X) and c.1634A > G (p.K545R) compound heterozygous mutations. . 2023-06-00. Pubmed ID: 37209469; DOI: 10.1016/j.scr.2023.103122 ONHi001-A 2023-06-00 2023-06-00 PubMed: 37209469 DOI: 10.1016/j.scr.2023.103122Associated cell lines:
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Zhang M, Yu M, Guo R, Zhang Y, Zhang X, Sun J, Zhang J, Wang X, Ma J
Human induced pluripotent stem cell (iPSC) line (HEBHMUi014-A) derived from a patient with Alzheimer's disease
Zhang M et al. Human induced pluripotent stem cell (iPSC) line (HEBHMUi014-A) derived from a patient with Alzheimer's disease. . 2023-06-00. Pubmed ID: 37178573; DOI: 10.1016/j.scr.2023.103116 HEBHMUi014-A 2023-06-00 2023-06-00 PubMed: 37178573 DOI: 10.1016/j.scr.2023.103116Associated cell lines:
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Zeng W, Kong X, Alamana C, Liu Y, Guzman J, Pang PD, Day JW, Wu JC
Generation of two induced pluripotent stem cell lines from spinal muscular atrophy type 1 patients carrying no functional copies of SMN1 gene
Zeng W et al. Generation of two induced pluripotent stem cell lines from spinal muscular atrophy type 1 patients carrying no functional copies of SMN1 gene. . 2023-06-00. Pubmed ID: 37087898; DOI: 10.1016/j.scr.2023.103095; PMC: PMC11068589 SCVIi001-ASCVIi002-ASCVIi075-ASCVIi076-A 2023-06-00 2023-06-00 PubMed: 37087898 DOI: 10.1016/j.scr.2023.103095Associated cell lines:
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Schottmann NM, Klug K, Klopocki E, Üçeyler N
Generation of induced pluripotent stem cell line (UKWNLi008) derived from a patient carrying a c.1678C>G variant in the transient receptor potential cation channel subfamily A member (TRPA1) gene potentially associated with small fiber neuropathy
Schottmann NM et al. Generation of induced pluripotent stem cell line (UKWNLi008) derived from a patient carrying a c.1678C>G variant in the transient receptor potential cation channel subfamily A member (TRPA1) gene potentially associated with small fiber neuropathy. . 2023-06-00. Pubmed ID: 37079968; DOI: 10.1016/j.scr.2023.103094 UKWNLi008-AUKWNLi008-BUKWNLi008-C 2023-06-00 2023-06-00 PubMed: 37079968 DOI: 10.1016/j.scr.2023.103094Associated cell lines:
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Placci Marina, Giannotti Marina I., Muro Silvia
Polymer-based drug delivery systems under investigation for enzyme replacement and other therapies of lysosomal storage disorders
Placci Marina et al. Polymer-based drug delivery systems under investigation for enzyme replacement and other therapies of lysosomal storage disorders. . 2023-06-00. DOI: 10.1016/j.addr.2022.114683 BRCi001-A 2023-06-00 2023-06-00 DOI: 10.1016/j.addr.2022.114683Associated cell lines:
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Vincent C, Lefort N, Hamlin M, Banal C, Hovnanian A, Izmiryan A
Generation and characterization of induced pluripotent stem cell lines from two patients with recessive dystrophic epidermolysis Bullosa
Vincent C et al. Generation and characterization of induced pluripotent stem cell lines from two patients with recessive dystrophic epidermolysis Bullosa. . 2023-06-00. Pubmed ID: 37148821; DOI: 10.1016/j.scr.2023.103104 IMAGINi002-AIMAGINi003-A 2023-06-00 2023-06-00 PubMed: 37148821 DOI: 10.1016/j.scr.2023.103104Associated cell lines:
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Tang Yuanzhang, Zhou Yang, Lin Guanyou, Zhang Miqin
Enhanced Cell Penetration and Pluripotency Maintenance of hiPSCs in 3D Natural Chitosan Scaffolds
Tang Yuanzhang et al. Enhanced Cell Penetration and Pluripotency Maintenance of hiPSCs in 3D Natural Chitosan Scaffolds. . 2023-06-00. DOI: 10.1002/mabi.202200460 JUCTCi010-A 2023-06-00 2023-06-00 DOI: 10.1002/mabi.202200460Associated cell lines:
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Correia JS, Duarte-Silva S, Salgado AJ, Maciel P
Cell-based therapeutic strategies for treatment of spinocerebellar ataxias: an update
Correia JS et al. Cell-based therapeutic strategies for treatment of spinocerebellar ataxias: an update. . 2023-06-00. Pubmed ID: 36453395; DOI: 10.4103/1673-5374.355981; PMC: PMC9838137 CHOPi002-ACHOPi003-AZZUNEUi002-ACSUXHi005-ARCPCMi008-A 2023-06-00 2023-06-00 PubMed: 36453395 DOI: 10.4103/1673-5374.355981Associated cell lines:
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Takasaki K, Kumar SS, Gagne A, French DL, Chou ST
Generation of 2 isogenic clones from a patient with Trisomy 21 and a GATA1 mutation
Takasaki K et al. Generation of 2 isogenic clones from a patient with Trisomy 21 and a GATA1 mutation. . 2023-06-00. Pubmed ID: 37084616; DOI: 10.1016/j.scr.2023.103098; PMC: PMC10576909 CHOPi002-ACHOPi003-ACHOPi008-ACHOPi008-C 2023-06-00 2023-06-00 PubMed: 37084616 DOI: 10.1016/j.scr.2023.103098Associated cell lines:
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Ukaji T, Takahashi-Shibata M, Arai D, Tsutsumi H, Tajima S, Akamatsu W, Matsumoto F, Ikeda K, Usami SI, Kamiya K
Generation and characterization of a human iPSC line (JUFMDOi007-A) from a patient with Usher syndrome due to mutation in USH2A
Ukaji T et al. Generation and characterization of a human iPSC line (JUFMDOi007-A) from a patient with Usher syndrome due to mutation in USH2A. . 2023-06-00. Pubmed ID: 37099934; DOI: 10.1016/j.scr.2023.103100 JUFMDOi007-A 2023-06-00 2023-06-00 PubMed: 37099934 DOI: 10.1016/j.scr.2023.103100Associated cell lines:
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Wijesinghe Printha, Xi Jeanne, Cui Jing, Campbell Matthew, Pham Wellington, Matsubara Joanne A
MicroRNAs in tear fluids predict underlying molecular changes associated with Alzheimer’s disease
Wijesinghe Printha et al. MicroRNAs in tear fluids predict underlying molecular changes associated with Alzheimer’s disease. . 2023-06-00. DOI: 10.26508/lsa.202201757 UMi038-AUMi039-A 2023-06-00 2023-06-00 DOI: 10.26508/lsa.202201757 -
Lee J, Baek H, Jang J, Park J, Cha SR, Hong SH, Kim J, Lee JH, Hong IS, Wang SJ, Lee JY, Song MH, Yang SR
Establishment of a human induced pluripotent stem cell derived alveolar organoid for toxicity assessment
Lee J et al. Establishment of a human induced pluripotent stem cell derived alveolar organoid for toxicity assessment. . 2023-06-00. Pubmed ID: 36931533; DOI: 10.1016/j.tiv.2023.105585 KRIBBi001-A 2023-06-00 2023-06-00 PubMed: 36931533 DOI: 10.1016/j.tiv.2023.105585Associated cell lines:
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Moore Lindsay Scott, Stankovic Konstantina M.
The Future of Vestibular Schwannoma Management
Moore Lindsay Scott et al. The Future of Vestibular Schwannoma Management. . 2023-06-00. DOI: 10.1016/j.otc.2023.02.018 HVRDi004-B-2 2023-06-00 2023-06-00 DOI: 10.1016/j.otc.2023.02.018Associated cell lines:
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Chatterjee Diptaman, Krainc Dimitri
Mechanisms of Glucocerebrosidase Dysfunction in Parkinson’s Disease
Chatterjee Diptaman et al. Mechanisms of Glucocerebrosidase Dysfunction in Parkinson’s Disease. . 2023-06-00. DOI: 10.1016/j.jmb.2023.168023 PNUSCRi001-A 2023-06-00 2023-06-00 DOI: 10.1016/j.jmb.2023.168023Associated cell lines:
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Fan Y, Li Y, Yang X, Zhang H, Wang B, Guan J, Gao J, Ma X, Liu Y
Generation and characterization of PBMCs-derived human induced pluripotent stem cell (iPSC) line SDQLCHi051-A from an autism spectrum disorder patient with compound CHD8 gene mutations
Fan Y et al. Generation and characterization of PBMCs-derived human induced pluripotent stem cell (iPSC) line SDQLCHi051-A from an autism spectrum disorder patient with compound CHD8 gene mutations. . 2023-06-00. Pubmed ID: 37229974; DOI: 10.1016/j.scr.2023.103114 SDQLCHi051-A 2023-06-00 2023-06-00 PubMed: 37229974 DOI: 10.1016/j.scr.2023.103114Associated cell lines:
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Xu J, Fu Y, Xia W, He J, Zou Y, Ruan W, Lou Q, Li Y, Pan J, Li H, Chen W
Corrigendum to "Generation of induced pluripotent stem cell line, ZJUCHi002-A, from Charcot-Marie-Tooth disease type 2A (CMT2A) patient with a mutation of c.752C>T in MFN2" [Stem Cell Res. 36C (2019) 101411]
Xu J et al. Corrigendum to "Generation of induced pluripotent stem cell line, ZJUCHi002-A, from Charcot-Marie-Tooth disease type 2A (CMT2A) patient with a mutation of c.752C>T in MFN2" [Stem Cell Res. 36C (2019) 101411]. . 2023-06-00. Pubmed ID: 37116346; DOI: 10.1016/j.scr.2023.103107 ZJUCHi002-A 2023-06-00 2023-06-00 PubMed: 37116346 DOI: 10.1016/j.scr.2023.103107Associated cell lines:
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Devito LG, Lionello VM, Muntoni F, Tedesco FS, Healy L
Generation of an MTM1-mutant iPSC line (CRICKi008-A) from an individual with X-linked myotubular myopathy (XLMTM)
Devito LG et al. Generation of an MTM1-mutant iPSC line (CRICKi008-A) from an individual with X-linked myotubular myopathy (XLMTM). . 2023-06-00. Pubmed ID: 36989620; DOI: 10.1016/j.scr.2023.103079 CRICKi001-ACRICKi008-A 2023-06-00 2023-06-00 PubMed: 36989620 DOI: 10.1016/j.scr.2023.103079Associated cell lines:
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Chitrangi S, Vaity P, Jamdar A, Patel H, Bhatt S
Generation of Human Induced Pluripotent Stem Cell line from PBMCs of Healthy Donors using Integration-free Sendai virus Technology
Chitrangi S et al. Generation of Human Induced Pluripotent Stem Cell line from PBMCs of Healthy Donors using Integration-free Sendai virus Technology. . 2023-06-00. Pubmed ID: 36905819; DOI: 10.1016/j.scr.2023.103062 YBLi001-AYBLi002-AYBLi003-A 2023-06-00 2023-06-00 PubMed: 36905819 DOI: 10.1016/j.scr.2023.103062 -
Sinha A, Guru SA, Varadarajan S, Alvarez A, Kaushal S, Fu X
Generation of a human induced pluripotent stem cell line from a pediatric heart failure patient with de novo DNM1L mutation
Sinha A et al. Generation of a human induced pluripotent stem cell line from a pediatric heart failure patient with de novo DNM1L mutation. . 2023-06-00. Pubmed ID: 37086582; DOI: 10.1016/j.scr.2023.103092 LCHi003-A 2023-06-00 2023-06-00 PubMed: 37086582 DOI: 10.1016/j.scr.2023.103092Associated cell lines:
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Ura H, Togi S, Ozaki M, Hatanaka H, Niida Y
Establishment of a human induced pluripotent stem cell line, KMUGMCi007-A, from a patient with prolidase deficiency (PD) bearing homozygous in-frame mutation in the PEPD gene
Ura H et al. Establishment of a human induced pluripotent stem cell line, KMUGMCi007-A, from a patient with prolidase deficiency (PD) bearing homozygous in-frame mutation in the PEPD gene. . 2023-06-00. Pubmed ID: 37023562; DOI: 10.1016/j.scr.2023.103075 KMUGMCi007-A 2023-06-00 2023-06-00 PubMed: 37023562 DOI: 10.1016/j.scr.2023.103075Associated cell lines:
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Lahm H, Stieglbauer S, Neb I, Doppler S, Schneider S, Dzilic E, Lange R, Krane M, Dreßen M
Generation of three CRISPR/Cas9 edited human induced pluripotent stem cell lines (DHMi005-A-5, DHMi005-A-6 and DHMi005-A-7) carrying a Holt-Oram Syndrome patient-specific TBX5 mutation with known cardiac phenotype and a FLAG-tag after exon 9 of the TBX5 gene
Lahm H et al. Generation of three CRISPR/Cas9 edited human induced pluripotent stem cell lines (DHMi005-A-5, DHMi005-A-6 and DHMi005-A-7) carrying a Holt-Oram Syndrome patient-specific TBX5 mutation with known cardiac phenotype and a FLAG-tag after exon 9 of the TBX5 gene. . 2023-06-00. Pubmed ID: 37210946; DOI: 10.1016/j.scr.2023.103123 DHMi005-ADHMi005-A-5DHMi005-A-6DHMi005-A-7 2023-06-00 2023-06-00 PubMed: 37210946 DOI: 10.1016/j.scr.2023.103123Associated cell lines:
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Qiu S, Zhang X, Zhang L, Liu Z, Wang L, Jin ZB, Xiao P
Generation of the induced pluripotent stem cell line SFMUi001-A from a patient with usher syndrome type 2 caused by biallelic variants in the USH2A gene
Qiu S et al. Generation of the induced pluripotent stem cell line SFMUi001-A from a patient with usher syndrome type 2 caused by biallelic variants in the USH2A gene. . 2023-06-00. Pubmed ID: 37126974; DOI: 10.1016/j.scr.2023.103101 SFMUi001-A 2023-06-00 2023-06-00 PubMed: 37126974 DOI: 10.1016/j.scr.2023.103101Associated cell lines:
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Alsalloum A, Mityaeva O, Kegeles E, Khavina E, Volchkov P
Generation of two human induced pluripotent stem cell lines (ABi001-A and ABi002-A) from cone dystrophy with supernormal rod response patients caused by KCNV2 mutation
Alsalloum A et al. Generation of two human induced pluripotent stem cell lines (ABi001-A and ABi002-A) from cone dystrophy with supernormal rod response patients caused by KCNV2 mutation. . 2023-06-00. Pubmed ID: 37121194; DOI: 10.1016/j.scr.2023.103099 ABi001-AABi002-AABi004-A 2023-06-00 2023-06-00 PubMed: 37121194 DOI: 10.1016/j.scr.2023.103099 -
Kamaldinov T, Zhang L, Wang L, Ye Z
Generation of induced pluripotent stem cell lines from helper and cytotoxic T cells of healthy individuals
Kamaldinov T et al. Generation of induced pluripotent stem cell lines from helper and cytotoxic T cells of healthy individuals. . 2023-06-00. Pubmed ID: 37156062; DOI: 10.1016/j.scr.2023.103113 OTATi001-AOTATi002-A 2023-06-00 2023-06-00 PubMed: 37156062 DOI: 10.1016/j.scr.2023.103113Associated cell lines:
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Qin Y, Zhan JQ, Ma CJ, Cao CY, Zhang Y, Min YT, Lv YF
Generation and characterization of iPS cell line (CTGUi001-A) from skin fibroblasts of a patient with Fabry disease
Qin Y et al. Generation and characterization of iPS cell line (CTGUi001-A) from skin fibroblasts of a patient with Fabry disease. . 2023-06-00. Pubmed ID: 36917862; DOI: 10.1016/j.scr.2023.103063 CTGUi001-A 2023-06-00 2023-06-00 PubMed: 36917862 DOI: 10.1016/j.scr.2023.103063Associated cell lines:
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Babaniyi Olusegun, Lalande Marc, Covault Jonathan
Modelling acute glucocorticoid transcriptome response in human embryonic stem cell derived neural cultures
Babaniyi Olusegun et al. Modelling acute glucocorticoid transcriptome response in human embryonic stem cell derived neural cultures. . 2023-06-00. DOI: 10.1016/j.scr.2023.103086 WAe001-AWAe009-A 2023-06-00 2023-06-00 DOI: 10.1016/j.scr.2023.103086 -
Alkobtawi M, Pla P, Onteniente B, Seal S, Pingault V, Marlin S, Monsoro-Burq AH
Two induced pluripotent stem cell (iPSC) lines derived from patients affected by Waardenburg syndrome type 1 retain potential to activate neural crest markers
Alkobtawi M et al. Two induced pluripotent stem cell (iPSC) lines derived from patients affected by Waardenburg syndrome type 1 retain potential to activate neural crest markers. . 2023-06-00. Pubmed ID: 36989619; DOI: 10.1016/j.scr.2023.103074; PMC: PMC10240564 PCIi029-APCIi031-A 2023-06-00 2023-06-00 PubMed: 36989619 DOI: 10.1016/j.scr.2023.103074 -
Akter M, Cui H, Abir Hosain M, Ding B
Generation of two induced pluripotent stem cell lines with heterozygous and homozygous amyotrophic lateral sclerosis-causing mutation P525L (c.1574C > T) in FUS gene
Akter M et al. Generation of two induced pluripotent stem cell lines with heterozygous and homozygous amyotrophic lateral sclerosis-causing mutation P525L (c.1574C > T) in FUS gene. . 2023-06-00. Pubmed ID: 37116345; DOI: 10.1016/j.scr.2023.103103; PMC: PMC10262954 UCSFi001-AUCSFi001-A-74UCSFi001-A-75 2023-06-00 2023-06-00 PubMed: 37116345 DOI: 10.1016/j.scr.2023.103103Associated cell lines:
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Van Gucht I, Buccioli L, Rabaut L, Fedoryshchenko I, Meester J, Van Laer L, Loeys B, Verstraeten A
Generation of one induced pluripotent cell (iPSC) line (BBANTWi011-A) from a patient carrying an IPO8 bi-allelic loss-of-function mutation
Van Gucht I et al. Generation of one induced pluripotent cell (iPSC) line (BBANTWi011-A) from a patient carrying an IPO8 bi-allelic loss-of-function mutation. . 2023-06-00. Pubmed ID: 36905820; DOI: 10.1016/j.scr.2023.103061 BBANTWi011-A 2023-06-00 2023-06-00 PubMed: 36905820 DOI: 10.1016/j.scr.2023.103061Associated cell lines:
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Rädecke K, Gore A, Burau K, Laugsch M, Köhler K, Rappold GA, Hoffmann S
Generation of two homozygous SHOX2 knock-out human induced pluripotent stem cell lines using CRISPR/Cas9
Rädecke K et al. Generation of two homozygous SHOX2 knock-out human induced pluripotent stem cell lines using CRISPR/Cas9. . 2023-06-00. Pubmed ID: 37028180; DOI: 10.1016/j.scr.2023.103089 MRIi016-A-1MRIi016-A-2DPEDi001-ADPEDi001-A-1 2023-06-00 2023-06-00 PubMed: 37028180 DOI: 10.1016/j.scr.2023.103089Associated cell lines:
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Xu J, Wang Y, He J, Xia W, Zou Y, Ruan W, Lou Q, Li Y, Li H, Chen W
Corrigendum to "Generation of a human Charcot-Marie-Tooth disease type 1B (CMT1B) iPSC line, ZJUCHi001-A, with a mutation of c.292C>T in MPZ" [Stem Cell Res. 35C (2019) 101407]
Xu J et al. Corrigendum to "Generation of a human Charcot-Marie-Tooth disease type 1B (CMT1B) iPSC line, ZJUCHi001-A, with a mutation of c.292C>T in MPZ" [Stem Cell Res. 35C (2019) 101407]. . 2023-06-00. Pubmed ID: 37116344; DOI: 10.1016/j.scr.2023.103106 ZJUCHi001-A 2023-06-00 2023-06-00 PubMed: 37116344 DOI: 10.1016/j.scr.2023.103106Associated cell lines:
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Han Wenjie, Li Zhigang, Guo Yijun, He Kaining, Li Wenqing, Xu Caoling, Ge Lishuang, He Miao, Yin Xue, Zhou Junxiang, Li Chengxu, Yao Dongbao, Bao Jianqiang, Liang Haojun
Efficient precise integration of large DNA sequences with 3′-overhang dsDNA donors using CRISPR/Cas9
Han Wenjie et al. Efficient precise integration of large DNA sequences with 3′-overhang dsDNA donors using CRISPR/Cas9. . 2023-05-30. DOI: 10.1073/pnas.2221127120 CSUi002-ACSUi002-A-1 2023-05-30 2023-05-30 DOI: 10.1073/pnas.2221127120Associated cell lines:
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Xu Ziran, Yang Jiaxu, Xin Xianyi, Liu Chengrun, Li Lisha, Mei Xianglin, Li Meiying
Merits and challenges of iPSC-derived organoids for clinical applications
Xu Ziran et al. Merits and challenges of iPSC-derived organoids for clinical applications. . 2023-05-26. DOI: 10.3389/fcell.2023.1188905 UNIPDi001-A 2023-05-26 2023-05-26 DOI: 10.3389/fcell.2023.1188905Associated cell lines:
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Valerio Luis Sebastian Alexis, Carrick Frederick Robert, Bedoya Lina, Sreerama Sandeep, Sugaya Kiminobu
Neural Differentiation of Induced Pluripotent Stem Cells for a Xenogeneic Material-Free 3D Neurological Disease Model Neurulation from Pluripotent Cells Using a Human Hydrogel
Valerio Luis Sebastian Alexis et al. Neural Differentiation of Induced Pluripotent Stem Cells for a Xenogeneic Material-Free 3D Neurological Disease Model Neurulation from Pluripotent Cells Using a Human Hydrogel. . 2023-05-25. DOI: 10.3390/cimb45060290 IRMBi001-A 2023-05-25 2023-05-25 DOI: 10.3390/cimb45060290Associated cell lines:
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von Schledorn L, Puertollano Martín D, Cleve N, Zöllner J, Roth D, Staar BO, Hegermann J, Ringshausen FC, Nawroth J, Martin U, Olmer R
Primary Ciliary Dyskinesia Patient-Specific hiPSC-Derived Airway Epithelium in Air-Liquid Interface Culture Recapitulates Disease Specific Phenotypes In Vitro
von Schledorn L et al. Primary Ciliary Dyskinesia Patient-Specific hiPSC-Derived Airway Epithelium in Air-Liquid Interface Culture Recapitulates Disease Specific Phenotypes In Vitro. . 2023-05-24. Pubmed ID: 37296588; DOI: 10.3390/cells12111467; PMC: PMC10252476 MHHi001-AMHHi012-AMHHi013-AMHHi014-AMHHi016-AMHHi016-BMHHi017-AMHHi017-BMHHi018-AMHHi019-AMHHi019-B 2023-05-24 2023-05-24 PubMed: 37296588 DOI: 10.3390/cells12111467 -
Soldati S, Bär A, Vladymyrov M, Glavin D, McGrath JL, Gosselet F, Nishihara H, Goelz S, Engelhardt B
High levels of endothelial ICAM-1 prohibit natalizumab mediated abrogation of CD4(+) T cell arrest on the inflamed BBB under flow in vitro
Soldati S et al. High levels of endothelial ICAM-1 prohibit natalizumab mediated abrogation of CD4(+) T cell arrest on the inflamed BBB under flow in vitro. . 2023-05-23. Pubmed ID: 37221552; DOI: 10.1186/s12974-023-02797-8; PMC: PMC10204262 LNISi002-BLNISi007-B 2023-05-23 2023-05-23 PubMed: 37221552 DOI: 10.1186/s12974-023-02797-8Associated cell lines:
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Kopytova AE, Rychkov GN, Cheblokov AA, Grigor'eva EV, Nikolaev MA, Yarkova ES, Sorogina DA, Ibatullin FM, Baydakova GV, Izyumchenko AD, Bogdanova DA, Boitsov VM, Rybakov AV, Miliukhina IV, Bezrukikh VA, Salogub GN, Zakharova EY, Pchelina SN, Emelyanov AK
Potential Binding Sites of Pharmacological Chaperone NCGC00241607 on Mutant β-Glucocerebrosidase and Its Efficacy on Patient-Derived Cell Cultures in Gaucher and Parkinson's Disease
Kopytova AE et al. Potential Binding Sites of Pharmacological Chaperone NCGC00241607 on Mutant β-Glucocerebrosidase and Its Efficacy on Patient-Derived Cell Cultures in Gaucher and Parkinson's Disease. . 2023-05-22. Pubmed ID: 37240451; DOI: 10.3390/ijms24109105; PMC: PMC10219579 ICGi021-AICGi022-AICGi034-AICGi034-BICGi034-C 2023-05-22 2023-05-22 PubMed: 37240451 DOI: 10.3390/ijms24109105 -
Tang Qiyu, Hu Zhiqing, Zhao Junya, Zhou Tao, Tang Shuqing, Wang Peiyun, Xiao Rou, Chen Yan, Wu Lingqian, Zhou Miaojin, Liang Desheng
CRISPR-Mediated In Situ Introduction or Integration of F9-Padua in Human iPSCs for Gene Therapy of Hemophilia B
Tang Qiyu et al. CRISPR-Mediated In Situ Introduction or Integration of F9-Padua in Human iPSCs for Gene Therapy of Hemophilia B. . 2023-05-19. DOI: 10.3390/ijms24109013 SMBCi013-A 2023-05-19 2023-05-19 DOI: 10.3390/ijms24109013Associated cell lines:
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Giannetti Federica, Barbieri Miriam, Shiti Assad, Casini Simona, Sager Philip T, Das Saumya, Pradhananga Sabindra, Srinivasan Dinesh, Nimani Saranda, Alerni Nicolò, Louradour Julien, Mura Manuela, Gnecchi Massimiliano, Brink Paul, Zehender Manfred, Koren Gideon, Zaza Antonio, Crotti Lia, Wilde Arthur A M, Schwartz Peter J, Remme Carol Ann, Gepstein Lior, Sala Luca, Odening Katja E
Gene- and variant-specific efficacy of serum/glucocorticoid-regulated kinase 1 inhibition in long QT syndrome types 1 and 2
Giannetti Federica et al. Gene- and variant-specific efficacy of serum/glucocorticoid-regulated kinase 1 inhibition in long QT syndrome types 1 and 2. . 2023-05-19. DOI: 10.1093/europace/euad094 PSMi004-A 2023-05-19 2023-05-19 DOI: 10.1093/europace/euad094Associated cell lines:
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Cheng Wei, Fan Chengming, Song Qing, Chen Ping, Peng Hong, Lin Ling, Liu Cong, Wang Bin, Zhou Zijing
Induced pluripotent stem cell-based therapies for organ fibrosis
Cheng Wei et al. Induced pluripotent stem cell-based therapies for organ fibrosis. . 2023-05-18. DOI: 10.3389/fbioe.2023.1119606 MHHi006-AMHHi006-A-1RCMGi001-AMHHi018-ARCMGi002-ARCMGi004-A 2023-05-18 2023-05-18 DOI: 10.3389/fbioe.2023.1119606Associated cell lines:
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Aydogmus H, Hu M, Ivancevic L, Frimat JP, van den Maagdenberg AMJM, Sarro PM, Mastrangeli M
An organ-on-chip device with integrated charge sensors and recording microelectrodes
Aydogmus H et al. An organ-on-chip device with integrated charge sensors and recording microelectrodes. . 2023-05-18. Pubmed ID: 37202451; DOI: 10.1038/s41598-023-34786-5; PMC: PMC10195821 LUMCi002-ALUMCi003-A 2023-05-18 2023-05-18 PubMed: 37202451 DOI: 10.1038/s41598-023-34786-5Associated cell lines:
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Chen Yanyan, Huang Pufeng, Niu Mengda, Tian Chuanhuizi, Zhang Tingting, Peng Zhiping
Regeneration of T cells from human-induced pluripotent stem cells for CAR-T cell medicated immunotherapy
Chen Yanyan et al. Regeneration of T cells from human-induced pluripotent stem cells for CAR-T cell medicated immunotherapy. . 2023-05-18. DOI: 10.3389/fbioe.2023.1159507 CIPi001-A 2023-05-18 2023-05-18 DOI: 10.3389/fbioe.2023.1159507Associated cell lines:
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Mendivil-Perez Miguel, Velez-Pardo Carlos, Lopera Francisco, Kosik Kenneth S., Jimenez-Del-Rio Marlene
PSEN1 E280A Cholinergic-like Neurons and Cerebral Spheroids Derived from Mesenchymal Stromal Cells and from Induced Pluripotent Stem Cells Are Neuropathologically Equivalent
Mendivil-Perez Miguel et al. PSEN1 E280A Cholinergic-like Neurons and Cerebral Spheroids Derived from Mesenchymal Stromal Cells and from Induced Pluripotent Stem Cells Are Neuropathologically Equivalent. . 2023-05-18. DOI: 10.3390/ijms24108957 IMEDEAi006-A 2023-05-18 2023-05-18 DOI: 10.3390/ijms24108957Associated cell lines:
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Lupan BM, Solecki RA, Musso CM, Alsina FC, Silver DL
The exon junction complex component EIF4A3 is essential for mouse and human cortical progenitor mitosis and neurogenesis
Lupan BM et al. The exon junction complex component EIF4A3 is essential for mouse and human cortical progenitor mitosis and neurogenesis. . 2023-05-15. Pubmed ID: 37139782; DOI: 10.1242/dev.201619; PMC: PMC10233715 WAe009-A 2023-05-15 2023-05-15 PubMed: 37139782 DOI: 10.1242/dev.201619Associated cell lines:
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Sambri I, Ferniani M, Campostrini G, Testa M, Meraviglia V, de Araujo MEG, Dokládal L, Vilardo C, Monfregola J, Zampelli N, Vecchio Blanco FD, Torella A, Ruosi C, Fecarotta S, Parenti G, Staiano L, Bellin M, Huber LA, De Virgilio C, Trepiccione F, Nigro V, Ballabio A
RagD auto-activating mutations impair MiT/TFE activity in kidney tubulopathy and cardiomyopathy syndrome
Sambri I et al. RagD auto-activating mutations impair MiT/TFE activity in kidney tubulopathy and cardiomyopathy syndrome. . 2023-05-15. Pubmed ID: 37188688; DOI: 10.1038/s41467-023-38428-2; PMC: PMC10185561 ESi007-ALUMCi028-A 2023-05-15 2023-05-15 PubMed: 37188688 DOI: 10.1038/s41467-023-38428-2Associated cell lines:
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Ma Shize, Li Xiu, Cao Rui, Zhan Guoqin, Fu Xin, Xiao Ran, Yang Zhigang
Developmentally regulated expression of integrin alpha-6 distinguishes neural crest derivatives in the skin
Ma Shize et al. Developmentally regulated expression of integrin alpha-6 distinguishes neural crest derivatives in the skin. . 2023-05-15. DOI: 10.3389/fcell.2023.1140554 JTUi002-A 2023-05-15 2023-05-15 DOI: 10.3389/fcell.2023.1140554Associated cell lines:
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Rani Sonam, Thamodaran Vasanth, Nandy Krittika, Aboobacker Fouzia Nambiathayil, Maddali Madhavi, Rajesh Praveena, Vijayanand S, David Ernest, Velayudhan Shaji Ramachandran
Establishment and characterization of CSCRi006-A: An induced pluripotent stem cell line generated from a patient with Diamond-Blackfan Anemia (DBA) carrying ribosomal protein S19 (RPS19) mutation.
Rani Sonam et al. Establishment and characterization of CSCRi006-A: An induced pluripotent stem cell line generated from a patient with Diamond-Blackfan Anemia (DBA) carrying ribosomal protein S19 (RPS19) mutation. . 2023-05-12. DOI: 10.21203/rs.3.rs-2876104/v1 CSCRi006-A 2023-05-12 2023-05-12 DOI: 10.21203/rs.3.rs-2876104/v1Associated cell lines:
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Eisen Binyamin, Binah Ofer
Modeling Duchenne Muscular Dystrophy Cardiomyopathy with Patients’ Induced Pluripotent Stem-Cell-Derived Cardiomyocytes
Eisen Binyamin et al. Modeling Duchenne Muscular Dystrophy Cardiomyopathy with Patients’ Induced Pluripotent Stem-Cell-Derived Cardiomyocytes. . 2023-05-12. DOI: 10.3390/ijms24108657 IITi001-A 2023-05-12 2023-05-12 DOI: 10.3390/ijms24108657Associated cell lines:
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Rossiaud Lucille, Fragner Pascal, Barbon Elena, Gardin Antoine, Benabides Manon, Pellier Emilie, Cosette Jérémie, El Kassar Lina, Giraud-Triboult Karine, Nissan Xavier, Ronzitti Giuseppe, Hoch Lucile
Pathological modeling of glycogen storage disease type III with CRISPR/Cas9 edited human pluripotent stem cells
Rossiaud Lucille et al. Pathological modeling of glycogen storage disease type III with CRISPR/Cas9 edited human pluripotent stem cells. . 2023-05-11. DOI: 10.3389/fcell.2023.1163427 CSCRMi001-A 2023-05-11 2023-05-11 DOI: 10.3389/fcell.2023.1163427Associated cell lines:
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Reisqs J. B., Moreau A., Sleiman Y., Boutjdir M., Richard S., Chevalier P.
Arrhythmogenic cardiomyopathy as a myogenic disease: highlights from cardiomyocytes derived from human induced pluripotent stem cells
Reisqs J. B. et al. Arrhythmogenic cardiomyopathy as a myogenic disease: highlights from cardiomyocytes derived from human induced pluripotent stem cells. . 2023-05-11. DOI: 10.3389/fphys.2023.1191965 CBRCULi001-ACBRCULi002-ACBRCULi003-ACBRCULi004-ACBRCULi005-A 2023-05-11 2023-05-11 DOI: 10.3389/fphys.2023.1191965Associated cell lines:
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Lamandé SR, Ng ES, Cameron TL, Kung LHW, Sampurno L, Rowley L, Lilianty J, Patria YN, Stenta T, Hanssen E, Bell KM, Saxena R, Stok KS, Stanley EG, Elefanty AG, Bateman JF
Modeling human skeletal development using human pluripotent stem cells
Lamandé SR et al. Modeling human skeletal development using human pluripotent stem cells. . 2023-05-09. Pubmed ID: 37126720; DOI: 10.1073/pnas.2211510120; PMC: PMC10175848 MCRIi001-AMCRIi018-AMCRIi018-BMCRIi001-A-2MCRIi019-AMCRIi019-A-2MCRIi019-A-7 2023-05-09 2023-05-09 PubMed: 37126720 DOI: 10.1073/pnas.2211510120Associated cell lines:
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Wen J, Zellner A, Braun NC, Bajaj T, Gassen NC, Peitz M, Brüstle O
Loss of function of FIP200 in human pluripotent stem cell-derived neurons leads to axonal pathology and hyperactivity
Wen J et al. Loss of function of FIP200 in human pluripotent stem cell-derived neurons leads to axonal pathology and hyperactivity. . 2023-05-03. Pubmed ID: 37137886; DOI: 10.1038/s41398-023-02432-3; PMC: PMC10156752 UKBi017-A 2023-05-03 2023-05-03 PubMed: 37137886 DOI: 10.1038/s41398-023-02432-3Associated cell lines:
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Kerkhof Laurie M.C., Warrenburg Bart P.C. van de, Roon-Mom Willeke M.C. van, Buijsen Ronald A.M.
Therapeutic Strategies for Spinocerebellar Ataxia Type 1
Kerkhof Laurie M.C. et al. Therapeutic Strategies for Spinocerebellar Ataxia Type 1. . 2023-05-02. DOI: 10.3390/biom13050788 LUMCi002-ALUMCi003-A 2023-05-02 2023-05-02 DOI: 10.3390/biom13050788Associated cell lines:
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Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: Hybrid Posters
(unknown author). Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: Hybrid Posters. . 2023-05-01. FRIMOi006-A 2023-05-01 2023-05-01Associated cell lines:
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von Bibra C, Shibamiya A, Bähr A, Geertz B, Köhne M, Stuedemann T, Starbatty J, Horneffer-van der Sluis V, Klostermeier UC, Hornaschewitz N, Li X, Wolf E, Klymiuk N, Krane M, Kupatt C, Hiebl B, Eschenhagen T, Weinberger F
Immature human engineered heart tissues engraft in a guinea pig chronic injury model
von Bibra C et al. Immature human engineered heart tissues engraft in a guinea pig chronic injury model. . 2023-05-01. Pubmed ID: 37272385; DOI: 10.1242/dmm.049834; PMC: PMC10259837 UKEi001-A 2023-05-01 2023-05-01 PubMed: 37272385 DOI: 10.1242/dmm.049834Associated cell lines:
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Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
(unknown author). Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters. . 2023-05-01. RCMGi001-A 2023-05-01 2023-05-01Associated cell lines:
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Kopytova A, Rychkov G, Cheblokov A, Grigor’eva E, Nikolaev M, Yarkova E, Sorogina D, Ibatullin F, Baydakova G, Izyumchenko A, Bogdanova D, Boitsov V, Rybakov A, Miliukhina I, Bezrukikh V, Salogub G, Zakharova E, Pchelina S, Emelyanov A.
Potential Binding Sites of Pharmacological Chaperone NCGC00241607 on Mutant β-Glucocerebrosidase and Its Efficacy on Patient-Derived Cell Cultures in Gaucher and Parkinson’s Disease
Kopytova A et al. Potential Binding Sites of Pharmacological Chaperone NCGC00241607 on Mutant β-Glucocerebrosidase and Its Efficacy on Patient-Derived Cell Cultures in Gaucher and Parkinson’s Disease. . 2023-05-01. ICGi021-AICGi022-AICGi034-AICGi034-BICGi034-C 2023-05-01 2023-05-01 -
Zhou L.
Clinical features of 6 children with uridine-responsive developmental epileptic encephalopathy 50 caused by CAD gene variants
Zhou L.. Clinical features of 6 children with uridine-responsive developmental epileptic encephalopathy 50 caused by CAD gene variants. . 2023-05-01. DOI: 10.3760/cma.j.cn112140-20221108-00950 BCHNCi001-A 2023-05-01 2023-05-01 DOI: 10.3760/cma.j.cn112140-20221108-00950Associated cell lines:
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Zhoulideh Yalda, Joolideh Jamil
CHARGE syndrome, from occurrence to treatment
Zhoulideh Yalda et al. CHARGE syndrome, from occurrence to treatment. . 2023-05-00. DOI: 10.1016/j.humgen.2023.201176 FDCHi009-A 2023-05-00 2023-05-00 DOI: 10.1016/j.humgen.2023.201176Associated cell lines:
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Fan L, Zhang S, Li X, Hu Z, Yang J, Zhang S, Zheng H, Su Y, Luo H, Liu X, Fan Y, Sun H, Zhang Z, Miao J, Song B, Xia Z, Shi C, Mao C, Xu Y
CHCHD2 p.Thr61Ile knock-in mice exhibit motor defects and neuropathological features of Parkinson's disease
Fan L et al. CHCHD2 p.Thr61Ile knock-in mice exhibit motor defects and neuropathological features of Parkinson's disease. . 2023-05-00. Pubmed ID: 36322611; DOI: 10.1111/bpa.13124; PMC: PMC10154378 ZZUi007-A 2023-05-00 2023-05-00 PubMed: 36322611 DOI: 10.1111/bpa.13124Associated cell lines:
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Bose Bipasha, Nihad Muhammad, P Sudheer Shenoy
Pluripotent stem cells: Basic biology or else differentiations aimed at translational research and the role of flow cytometry
Bose Bipasha et al. Pluripotent stem cells: Basic biology or else differentiations aimed at translational research and the role of flow cytometry. . 2023-05-00. DOI: 10.1002/cyto.a.24726 IPTi005-AIPTi007-AITXi001-AITXi001-A-1 2023-05-00 2023-05-00 DOI: 10.1002/cyto.a.24726Associated cell lines:
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Li Lu, Zhang Lingling, Cao Yingjie, Chen Xu, Gong Haifeng, Ma Yidan, Gui Yuanyuan, Xiang Tianya, Liu Jianxing, Huang Xinzhong
NDUFV1 attenuates renal ischemia–reperfusion injury by improving mitochondrial homeostasis
Li Lu et al. NDUFV1 attenuates renal ischemia–reperfusion injury by improving mitochondrial homeostasis. . 2023-05-00. DOI: 10.1111/jcmm.17735 UOMi002-A 2023-05-00 2023-05-00 DOI: 10.1111/jcmm.17735Associated cell lines:
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Heidari Khoei H, Javali A, Kagawa H, Sommer TM, Sestini G, David L, Slovakova J, Novatchkova M, Scholte Op Reimer Y, Rivron N
Generating human blastoids modeling blastocyst-stage embryos and implantation
Heidari Khoei H et al. Generating human blastoids modeling blastocyst-stage embryos and implantation. . 2023-05-00. Pubmed ID: 36792779; DOI: 10.1038/s41596-023-00802-1; PMC: PMC7617227 CAMe001-A 2023-05-00 2023-05-00 PubMed: 36792779 DOI: 10.1038/s41596-023-00802-1Associated cell lines:
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Saha B, Roy A, Beltramo E, Sahoo OS
Stem cells and diabetic retinopathy: From models to treatment
Saha B et al. Stem cells and diabetic retinopathy: From models to treatment. . 2023-05-00. Pubmed ID: 36842153; DOI: 10.1007/s11033-023-08337-0 CSUASOi008-A 2023-05-00 2023-05-00 PubMed: 36842153 DOI: 10.1007/s11033-023-08337-0Associated cell lines:
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Han H, Rim YA, Ju JH
Recent updates of stem cell-based erythropoiesis
Han H et al. Recent updates of stem cell-based erythropoiesis. . 2023-05-00. Pubmed ID: 36754940; DOI: 10.1007/s13577-023-00872-z; PMC: PMC9908308 MUSIi001-AMUSIi011-A 2023-05-00 2023-05-00 PubMed: 36754940 DOI: 10.1007/s13577-023-00872-zAssociated cell lines:
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Mendoza-Castrejon J, Magee JA
Layered immunity and layered leukemogenicity: Developmentally restricted mechanisms of pediatric leukemia initiation
Mendoza-Castrejon J et al. Layered immunity and layered leukemogenicity: Developmentally restricted mechanisms of pediatric leukemia initiation. . 2023-05-00. Pubmed ID: 36588481; DOI: 10.1111/imr.13180; PMC: PMC10301262 CHOPi001-A 2023-05-00 2023-05-00 PubMed: 36588481 DOI: 10.1111/imr.13180Associated cell lines:
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Liu Huiting, Qiu Biying, Yang Huan, Zheng Wen, Luo Yingying, Zhong Yadan, Lu Ping, Chen Junyi, Luo Ying, Liu Jun, Yang Bin
AHNAK, regulated by the OSM/OSMR signaling, involved in the development of primary localized cutaneous amyloidosis
Liu Huiting et al. AHNAK, regulated by the OSM/OSMR signaling, involved in the development of primary localized cutaneous amyloidosis. . 2023-05-00. DOI: 10.1016/j.jdermsci.2023.04.004 WAe009-A-82 2023-05-00 2023-05-00 DOI: 10.1016/j.jdermsci.2023.04.004Associated cell lines:
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Rivera‐Arbeláez José M., Keekstra Danjel, Cofiño‐Fabres Carla, Boonen Tom, Dostanic Milica, ten Den Simone A., Vermeul Kim, Mastrangeli Massimo, van den Berg Albert, Segerink Loes I., Ribeiro Marcelo C., Strisciuglio Nicola, Passier Robert
Automated assessment of human engineered heart tissues using deep learning and template matching for segmentation and tracking
Rivera‐Arbeláez José M. et al. Automated assessment of human engineered heart tissues using deep learning and template matching for segmentation and tracking. . 2023-05-00. DOI: 10.1002/btm2.10513 ESIBIe003-ACDIi004-ALUMCi028-A 2023-05-00 2023-05-00 DOI: 10.1002/btm2.10513Associated cell lines:
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Breitmeyer R, Vogel S, Heider J, Hartmann SM, Wüst R, Keller AL, Binner A, Fitzgerald JC, Fallgatter AJ, Volkmer H
Regulation of synaptic connectivity in schizophrenia spectrum by mutual neuron-microglia interaction
Breitmeyer R et al. Regulation of synaptic connectivity in schizophrenia spectrum by mutual neuron-microglia interaction. . 2023-04-29. Pubmed ID: 37117634; DOI: 10.1038/s42003-023-04852-9; PMC: PMC10147621 NMIi001-ANMIi002-ANMIi004-ANMIi005-ANMIi006-ANMIi010-A 2023-04-29 2023-04-29 PubMed: 37117634 DOI: 10.1038/s42003-023-04852-9 -
Kettunen Pinja, Lesnikova Angelina, Räsänen Noora, Ojha Ravi, Palmunen Leena, Laakso Markku, Lehtonen Šárka, Kuusisto Johanna, Pietiläinen Olli, Saber Saber H., Joensuu Merja, Vapalahti Olli P., Koistinaho Jari, Rolova Taisia, Balistreri Giuseppe
SARS-CoV-2 Infection of Human Neurons Is TMPRSS2 Independent, Requires Endosomal Cell Entry, and Can Be Blocked by Inhibitors of Host Phosphoinositol-5 Kinase
Kettunen Pinja et al. SARS-CoV-2 Infection of Human Neurons Is TMPRSS2 Independent, Requires Endosomal Cell Entry, and Can Be Blocked by Inhibitors of Host Phosphoinositol-5 Kinase. . 2023-04-27. DOI: 10.1128/jvi.00144-23 UEFi003-A 2023-04-27 2023-04-27 DOI: 10.1128/jvi.00144-23Associated cell lines:
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Armendariz DA, Goetsch SC, Sundarrajan A, Sivakumar S, Wang Y, Xie S, Munshi NV, Hon GC
CHD-associated enhancers shape human cardiomyocyte lineage commitment
Armendariz DA et al. CHD-associated enhancers shape human cardiomyocyte lineage commitment. . 2023-04-25. Pubmed ID: 37096669; DOI: 10.7554/elife.86206; PMC: PMC10156167 WAe009-AWAe009-A-18 2023-04-25 2023-04-25 PubMed: 37096669 DOI: 10.7554/elife.86206Associated cell lines:
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Cani Alice, Tretti Parenzan Caterina, Frasson Chiara, Rampazzo Elena, Scarparo Pamela, Francescato Samuela, Caicci Federico, Barbieri Vito, Rosato Antonio, Cesaro Simone, Zecca Marco, Micalizzi Concetta, Sainati Laura, Pigazzi Martina, Biffi Alessandra, Buldini Barbara, Locatelli Franco, Persano Luca, Masetti Riccardo, te Kronnie Geertruij, Bresolin Silvia
Long-term proliferation of immature hypoxia-dependent JMML cells supported by a 3D in vitro system
Cani Alice et al. Long-term proliferation of immature hypoxia-dependent JMML cells supported by a 3D in vitro system. . 2023-04-25. DOI: 10.1182/bloodadvances.2021006746 CHOPi001-A 2023-04-25 2023-04-25 DOI: 10.1182/bloodadvances.2021006746Associated cell lines:
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LaLone V, Aizenshtadt A, Goertz J, Skottvoll FS, Mota MB, You J, Zhao X, Berg HE, Stokowiec J, Yu M, Schwendeman A, Scholz H, Wilson SR, Krauss S, Stevens MM
Quantitative chemometric phenotyping of three-dimensional liver organoids by Raman spectral imaging
LaLone V et al. Quantitative chemometric phenotyping of three-dimensional liver organoids by Raman spectral imaging. . 2023-04-24. Pubmed ID: 37159662; DOI: 10.1016/j.crmeth.2023.100440; PMC: PMC10162950 WTSIi013-AWTSIi028-A 2023-04-24 2023-04-24 PubMed: 37159662 DOI: 10.1016/j.crmeth.2023.100440Associated cell lines:
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Wang Xia, Wang Yingcan, Xu Ting, Fan Yanjie, Ding Yifeng, Qian Jihong
A novel compound heterozygous mutation of the CLCN7 gene is associated with autosomal recessive osteopetrosis
Wang Xia et al. A novel compound heterozygous mutation of the CLCN7 gene is associated with autosomal recessive osteopetrosis. . 2023-04-24. DOI: 10.3389/fped.2023.978879 BIHi002-A 2023-04-24 2023-04-24 DOI: 10.3389/fped.2023.978879Associated cell lines:
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Carvalho Sofia, Santos Juliana Inês, Moreira Luciana, Gonçalves Mariana, David Hugo, Matos Liliana, Encarnação Marisa, Alves Sandra, Coutinho Maria Francisca
Neurological Disease Modeling Using Pluripotent and Multipotent Stem Cells: A Key Step towards Understanding and Treating Mucopolysaccharidoses
Carvalho Sofia et al. Neurological Disease Modeling Using Pluripotent and Multipotent Stem Cells: A Key Step towards Understanding and Treating Mucopolysaccharidoses. . 2023-04-21. DOI: 10.3390/biomedicines11041234 IMEDEAi004-AIMEDEAi004-BBRCi001-AUNIGEi001-A 2023-04-21 2023-04-21 DOI: 10.3390/biomedicines11041234Associated cell lines:
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Zhou Jianli, Zhang Qiao, Zhao Yuzhen, Song Yuchen, Leng Yanan, Chen Moxian, Zhou Shaoming, Wang Zhaoxia
The regulatory role of alternative splicing in inflammatory bowel disease
Zhou Jianli et al. The regulatory role of alternative splicing in inflammatory bowel disease. . 2023-04-21. DOI: 10.3389/fimmu.2023.1095267 SDQLCHi012-A 2023-04-21 2023-04-21 DOI: 10.3389/fimmu.2023.1095267Associated cell lines:
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Tian G, Cao C, Li S, Wang W, Zhang Y, Lv Y
rAAV2-Mediated Restoration of GALC in Neural Stem Cells from Krabbe Patient-Derived iPSCs
Tian G et al. rAAV2-Mediated Restoration of GALC in Neural Stem Cells from Krabbe Patient-Derived iPSCs. . 2023-04-20. Pubmed ID: 37111381; DOI: 10.3390/ph16040624; PMC: PMC10143348 PUMCi001-A 2023-04-20 2023-04-20 PubMed: 37111381 DOI: 10.3390/ph16040624Associated cell lines:
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Lv Yafeng, Qin Yu, Wang Jing, Tian Guoshuai, Wang Wei, Cao Chunyu, Zhang Ye
Identifying altered developmental pathways in human globoid cell leukodystrophy iPSCs-derived NSCs using transcriptome profiling
Lv Yafeng et al. Identifying altered developmental pathways in human globoid cell leukodystrophy iPSCs-derived NSCs using transcriptome profiling. . 2023-04-19. DOI: 10.1186/s12864-023-09285-6 PUMCi001-APUMCi002-A 2023-04-19 2023-04-19 DOI: 10.1186/s12864-023-09285-6Associated cell lines:
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Castelo Rueda MP, Zanon A, Gilmozzi V, Lavdas AA, Raftopoulou A, Delcambre S, Del Greco M F, Klein C, Grünewald A, Pramstaller PP, Hicks AA, Pichler I
Molecular phenotypes of mitochondrial dysfunction in clinically non-manifesting heterozygous PRKN variant carriers
Castelo Rueda MP et al. Molecular phenotypes of mitochondrial dysfunction in clinically non-manifesting heterozygous PRKN variant carriers. . 2023-04-18. Pubmed ID: 37072441; DOI: 10.1038/s41531-023-00499-9; PMC: PMC10113363 STBCi033-BEURACi005-A 2023-04-18 2023-04-18 PubMed: 37072441 DOI: 10.1038/s41531-023-00499-9Associated cell lines:
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Lebedeva OS, Sharova EI, Grekhnev DA, Skorodumova LO, Kopylova IV, Vassina EM, Oshkolova A, Novikova IV, Krisanova AV, Olekhnovich EI, Vigont VA, Kaznacheyeva EV, Bogomazova AN, Lagarkova MA
An Efficient 2D Protocol for Differentiation of iPSCs into Mature Postmitotic Dopaminergic Neurons: Application for Modeling Parkinson's Disease
Lebedeva OS et al. An Efficient 2D Protocol for Differentiation of iPSCs into Mature Postmitotic Dopaminergic Neurons: Application for Modeling Parkinson's Disease. . 2023-04-14. Pubmed ID: 37108456; DOI: 10.3390/ijms24087297; PMC: PMC10139404 RCPCMi007-ARCPCMi007-A-1 2023-04-14 2023-04-14 PubMed: 37108456 DOI: 10.3390/ijms24087297Associated cell lines:
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Bashore FM, Marquez AB, Chaikuad A, Howell S, Dunn AS, Beltran AA, Smith JL, Drewry DH, Beltran AS, Axtman AD
Modulation of tau tubulin kinases (TTBK1 and TTBK2) impacts ciliogenesis
Bashore FM et al. Modulation of tau tubulin kinases (TTBK1 and TTBK2) impacts ciliogenesis. . 2023-04-14. Pubmed ID: 37059819; DOI: 10.1038/s41598-023-32854-4; PMC: PMC10104807 TMOi001-ATMOi001-A-9TMOi001-A-10 2023-04-14 2023-04-14 PubMed: 37059819 DOI: 10.1038/s41598-023-32854-4Associated cell lines:
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Astro V, Ramirez-Calderon G, Adamo A
Protocol to measure calcium spikes in cardiomyocytes obtained from human pluripotent stem cells using a ready-to-use media
Astro V et al. Protocol to measure calcium spikes in cardiomyocytes obtained from human pluripotent stem cells using a ready-to-use media. . 2023-04-13. Pubmed ID: 37060558; DOI: 10.1016/j.xpro.2023.102252; PMC: PMC10140149 WAe001-AKAUSTi011-AKAUSTi011-B 2023-04-13 2023-04-13 PubMed: 37060558 DOI: 10.1016/j.xpro.2023.102252Associated cell lines:
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Gehrlein A, Udayar V, Anastasi N, Morella ML, Ruf I, Brugger D, von der Mark S, Thoma R, Rufer A, Heer D, Pfahler N, Jochner A, Niewoehner J, Wolf L, Fueth M, Ebeling M, Villaseñor R, Zhu Y, Deen MC, Shan X, Ehsaei Z, Taylor V, Sidransky E, Vocadlo DJ, Freskgård PO, Jagasia R
Targeting neuronal lysosomal dysfunction caused by β-glucocerebrosidase deficiency with an enzyme-based brain shuttle construct
Gehrlein A et al. Targeting neuronal lysosomal dysfunction caused by β-glucocerebrosidase deficiency with an enzyme-based brain shuttle construct. . 2023-04-12. Pubmed ID: 37045813; DOI: 10.1038/s41467-023-37632-4; PMC: PMC10097658 BIONi010-CSTBCi025-C 2023-04-12 2023-04-12 PubMed: 37045813 DOI: 10.1038/s41467-023-37632-4Associated cell lines:
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Bogomiakova Margarita E., Sekretova Elizaveta K., Anufrieva Ksenia S., Khabarova Polina O., Kazakova Anastasia N., Bobrovsky Pavel A., Grigoryeva Tatiana V., Eremeev Artem V., Lebedeva Olga S., Bogomazova Alexandra N., Lagarkova Maria A.
iPSC-derived cells lack immune tolerance to autologous NK-cells due to imbalance in ligands for activating and inhibitory NK-cell receptors
Bogomiakova Margarita E. et al. iPSC-derived cells lack immune tolerance to autologous NK-cells due to imbalance in ligands for activating and inhibitory NK-cell receptors. . 2023-04-11. DOI: 10.1186/s13287-023-03308-5 RCPCMi007-ARCPCMi007-A-1RCPCMi008-A 2023-04-11 2023-04-11 DOI: 10.1186/s13287-023-03308-5Associated cell lines:
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Martins GLS, Nonaka CKV, Rossi EA, de Lima AVR, Adanho CSA, Oliveira MS, Yahouedehou SCMA, de Souza CLEM, Gonçalves MS, Paredes BD, Souza BSF
Evaluation of 2D and 3D Erythroid Differentiation Protocols Using Sickle Cell Disease and Healthy Donor Induced Pluripotent Stem Cells
Martins GLS et al. Evaluation of 2D and 3D Erythroid Differentiation Protocols Using Sickle Cell Disease and Healthy Donor Induced Pluripotent Stem Cells. . 2023-04-10. Pubmed ID: 37190030; DOI: 10.3390/cells12081121; PMC: PMC10137038 CBTCi003-ACBTCi005-ACBTCi006-ACBTCi007-AIGIBi001-A 2023-04-10 2023-04-10 PubMed: 37190030 DOI: 10.3390/cells12081121Associated cell lines:
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Yoo DH, Im YS, Oh JY, Gil D, Kim YO
DUSP6 is a memory retention feedback regulator of ERK signaling for cellular resilience of human pluripotent stem cells in response to dissociation
Yoo DH et al. DUSP6 is a memory retention feedback regulator of ERK signaling for cellular resilience of human pluripotent stem cells in response to dissociation. . 2023-04-07. Pubmed ID: 37029196; DOI: 10.1038/s41598-023-32567-8; PMC: PMC10082014 KSCBi002-ASNUe007-A 2023-04-07 2023-04-07 PubMed: 37029196 DOI: 10.1038/s41598-023-32567-8Associated cell lines:
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Marchiano S, Nakamura K, Reinecke H, Neidig L, Lai M, Kadota S, Perbellini F, Yang X, Klaiman JM, Blakely LP, Karbassi E, Fields PA, Fenix AM, Beussman KM, Jayabalu A, Kalucki FA, Potter JC, Futakuchi-Tsuchida A, Weber GJ, Dupras S, Tsuchida H, Pabon L, Wang L, Knollmann BC, Kattman S, Thies RS, Sniadecki N, MacLellan WR, Bertero A, Murry CE
Gene editing to prevent ventricular arrhythmias associated with cardiomyocyte cell therapy
Marchiano S et al. Gene editing to prevent ventricular arrhythmias associated with cardiomyocyte cell therapy. . 2023-04-06. Pubmed ID: 37028405; DOI: 10.1016/j.stem.2023.03.010; PMC: PMC10283080 RUESe002-A 2023-04-06 2023-04-06 PubMed: 37028405 DOI: 10.1016/j.stem.2023.03.010Associated cell lines:
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Wu Q, Wu J, Karim K, Chen X, Wang T, Iwama S, Carobbio S, Keen P, Vidal-Puig A, Kotter MR, Bassett A
Massively parallel characterization of CRISPR activator efficacy in human induced pluripotent stem cells and neurons
Wu Q et al. Massively parallel characterization of CRISPR activator efficacy in human induced pluripotent stem cells and neurons. . 2023-04-06. Pubmed ID: 36917981; DOI: 10.1016/j.molcel.2023.02.011; PMC: PMC10114495 WTSIi018-BWTSIi018-B-1CAMi014-A 2023-04-06 2023-04-06 PubMed: 36917981 DOI: 10.1016/j.molcel.2023.02.011Associated cell lines:
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Choi JB, Seol DW, Do HS, Yang HY, Kim TM, Byun YG, Park JM, Choi J, Hong SP, Chung WS, Suh JM, Koh GY, Lee BH, Wee G, Han YM
Fasudil alleviates the vascular endothelial dysfunction and several phenotypes of Fabry disease
Choi JB et al. Fasudil alleviates the vascular endothelial dysfunction and several phenotypes of Fabry disease. . 2023-04-05. Pubmed ID: 36755495; DOI: 10.1016/j.ymthe.2023.02.003; PMC: PMC10124081 DDLABi001-A 2023-04-05 2023-04-05 PubMed: 36755495 DOI: 10.1016/j.ymthe.2023.02.003Associated cell lines:
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Seibertz F, Sutanto H, Dülk R, Pronto JRD, Springer R, Rapedius M, Liutkute A, Ritter M, Jung P, Stelzer L, Hüsgen LM, Klopp M, Rubio T, Fakuade FE, Mason FE, Hartmann N, Pabel S, Streckfuss-Bömeke K, Cyganek L, Sossalla S, Heijman J, Voigt N
Electrophysiological and calcium-handling development during long-term culture of human-induced pluripotent stem cell-derived cardiomyocytes
Seibertz F et al. Electrophysiological and calcium-handling development during long-term culture of human-induced pluripotent stem cell-derived cardiomyocytes. . 2023-04-05. Pubmed ID: 37020075; DOI: 10.1007/s00395-022-00973-0; PMC: PMC10076390 UMGi014-C 2023-04-05 2023-04-05 PubMed: 37020075 DOI: 10.1007/s00395-022-00973-0Associated cell lines:
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Tolle I, Tiranti V, Prigione A
Modeling mitochondrial DNA diseases: from base editing to pluripotent stem-cell-derived organoids
Tolle I et al. Modeling mitochondrial DNA diseases: from base editing to pluripotent stem-cell-derived organoids. . 2023-04-05. Pubmed ID: 36876467; DOI: 10.15252/embr.202255678; PMC: PMC10074100 FINCBi002-AFINCBi003-A 2023-04-05 2023-04-05 PubMed: 36876467 DOI: 10.15252/embr.202255678Associated cell lines:
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Kraskovskaya Nina, Bolshakova Anastasia, Khotin Mikhail, Bezprozvanny Ilya, Mikhailova Natalia
Protocol Optimization for Direct Reprogramming of Primary Human Fibroblast into Induced Striatal Neurons
Kraskovskaya Nina et al. Protocol Optimization for Direct Reprogramming of Primary Human Fibroblast into Induced Striatal Neurons. . 2023-04-05. DOI: 10.3390/ijms24076799 ICGi033-A 2023-04-05 2023-04-05 DOI: 10.3390/ijms24076799Associated cell lines:
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Qian E, Uemura M, Kobayashi H, Nakamura S, Ozawa F, Yoshimatsu S, Ishikawa M, Onodera O, Morimoto S, Okano H
A human induced pluripotent stem cell model from a patient with hereditary cerebral small vessel disease carrying a heterozygous R302Q mutation in HTRA1
Qian E et al. A human induced pluripotent stem cell model from a patient with hereditary cerebral small vessel disease carrying a heterozygous R302Q mutation in HTRA1. . 2023-04-03. Pubmed ID: 37009886; DOI: 10.1186/s41232-023-00273-7; PMC: PMC10069112 KEIOi003-A 2023-04-03 2023-04-03 PubMed: 37009886 DOI: 10.1186/s41232-023-00273-7Associated cell lines:
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Melgari D, Calamaio S, Frosio A, Prevostini R, Anastasia L, Pappone C, Rivolta I
Automated Patch-Clamp and Induced Pluripotent Stem Cell-Derived Cardiomyocytes: A Synergistic Approach in the Study of Brugada Syndrome
Melgari D et al. Automated Patch-Clamp and Induced Pluripotent Stem Cell-Derived Cardiomyocytes: A Synergistic Approach in the Study of Brugada Syndrome. . 2023-04-03. Pubmed ID: 37047659; DOI: 10.3390/ijms24076687; PMC: PMC10095337 MUSIi009-AUMGi128-AMUSIi009-A-1BJTTHi001-ABJTTHi001-A-2BBANTWi006-ABBANTWi007-ASCVIi026-ASCVIi027-AIDIBGIi002-AIDIBGIi003-AIDIBGIi004-A 2023-04-03 2023-04-03 PubMed: 37047659 DOI: 10.3390/ijms24076687Associated cell lines:
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Zawada D, Kornherr J, Meier AB, Santamaria G, Dorn T, Nowak-Imialek M, Ortmann D, Zhang F, Lachmann M, Dreßen M, Ortiz M, Mascetti VL, Harmer SC, Nobles M, Tinker A, De Angelis MT, Pedersen RA, Grote P, Laugwitz KL, Moretti A, Goedel A
Retinoic acid signaling modulation guides in vitro specification of human heart field-specific progenitor pools
Zawada D et al. Retinoic acid signaling modulation guides in vitro specification of human heart field-specific progenitor pools. . 2023-04-03. Pubmed ID: 37012244; DOI: 10.1038/s41467-023-36764-x; PMC: PMC10070453 MRIi003-AMRIi018-ADHMi003-AMRIi003-A-8 2023-04-03 2023-04-03 PubMed: 37012244 DOI: 10.1038/s41467-023-36764-xAssociated cell lines:
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Boal Andrew M., McGrady Nolan R., Chamling Xitiz, Kagitapalli Bhanu S., Zack Donald J., Calkins David J., Risner Michael L.
Microfluidic Platforms Promote Polarization of Human-Derived Retinal Ganglion Cells That Model Axonopathy
Boal Andrew M. et al. Microfluidic Platforms Promote Polarization of Human-Derived Retinal Ganglion Cells That Model Axonopathy. . 2023-04-03. DOI: 10.1167/tvst.12.4.1 IGIBi005-A 2023-04-03 2023-04-03 DOI: 10.1167/tvst.12.4.1Associated cell lines:
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Wenjun H.
Establishment and identification of an efficient protocol for differentiation of endothelial cells from human induced pluripotent stem cells
Wenjun H.. Establishment and identification of an efficient protocol for differentiation of endothelial cells from human induced pluripotent stem cells. . 2023-04-01. DOI: 10.12307/2023.340 XACHi007-AXACHi008-AXACHi009-A 2023-04-01 2023-04-01 DOI: 10.12307/2023.340Associated cell lines:
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Lebedeva O, Sharova E, Grekhnev D, Skorodumova L, Kopylova I, Vassina E, Oshkolova A, Novikova I, Krisanova A, Olekhnovich E, Vigont V, Kaznacheyeva E, Bogomazova A, Lagarkova M.
An Efficient 2D Protocol for Differentiation of iPSCs into Mature Postmitotic Dopaminergic Neurons: Application for Modeling Parkinson’s Disease
Lebedeva O et al. An Efficient 2D Protocol for Differentiation of iPSCs into Mature Postmitotic Dopaminergic Neurons: Application for Modeling Parkinson’s Disease. . 2023-04-01. RCPCMi007-A 2023-04-01 2023-04-01Associated cell lines:
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Miller DC, Lisowski P, Genehr C, Wanker EE, Priller J, Prigione A, Diecke S
Generation of an induced pluripotent stem cell line from a Huntington's disease patient with a long HTT-PolyQ sequence
Miller DC et al. Generation of an induced pluripotent stem cell line from a Huntington's disease patient with a long HTT-PolyQ sequence. . 2023-04-00. Pubmed ID: 36863131; DOI: 10.1016/j.scr.2023.103056 BIHi035-A 2023-04-00 2023-04-00 PubMed: 36863131 DOI: 10.1016/j.scr.2023.103056Associated cell lines:
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Owen N, Toms M, Tian Y, Toualbi L, Richardson R, Young R, Tracey-White D, Dhami P, Beck S, Moosajee M
Loss of the crumbs cell polarity complex disrupts epigenetic transcriptional control and cell cycle progression in the developing retina
Owen N et al. Loss of the crumbs cell polarity complex disrupts epigenetic transcriptional control and cell cycle progression in the developing retina. . 2023-04-00. Pubmed ID: 36656098; DOI: 10.1002/path.6056; PMC: PMC10601974 UCLi016-AUCLi017-A 2023-04-00 2023-04-00 PubMed: 36656098 DOI: 10.1002/path.6056 -
Li ZA, Sant S, Cho SK, Goodman SB, Bunnell BA, Tuan RS, Gold MS, Lin H
Synovial joint-on-a-chip for modeling arthritis: progress, pitfalls, and potential
Li ZA et al. Synovial joint-on-a-chip for modeling arthritis: progress, pitfalls, and potential. . 2023-04-00. Pubmed ID: 35995600; DOI: 10.1016/j.tibtech.2022.07.011; PMC: PMC9938846 MCRIi019-AMCRIi019-A-7 2023-04-00 2023-04-00 PubMed: 35995600 DOI: 10.1016/j.tibtech.2022.07.011Associated cell lines:
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Peeters S, Fedoryshchenko I, Rabaut L, Verstraeten A, Loeys BL
Generation of an induced pluripotent stem cell (iPSC) line of a Marfan syndrome patient with a pathogenic FBN1 c.5372G > A (p.Cys1791Tyr) variant
Peeters S et al. Generation of an induced pluripotent stem cell (iPSC) line of a Marfan syndrome patient with a pathogenic FBN1 c.5372G > A (p.Cys1791Tyr) variant. . 2023-04-00. Pubmed ID: 36801568; DOI: 10.1016/j.scr.2023.103050 CMGANTi008-A 2023-04-00 2023-04-00 PubMed: 36801568 DOI: 10.1016/j.scr.2023.103050Associated cell lines:
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Subramaniam G, Schleicher K, Kovanich D, Zerio A, Folkmanaite M, Chao YC, Surdo NC, Koschinski A, Hu J, Scholten A, Heck AJR, Ercu M, Sholokh A, Park KC, Klussmann E, Meraviglia V, Bellin M, Zanivan S, Hester S, Mohammed S, Zaccolo M
Integrated Proteomics Unveils Nuclear PDE3A2 as a Regulator of Cardiac Myocyte Hypertrophy
Subramaniam G et al. Integrated Proteomics Unveils Nuclear PDE3A2 as a Regulator of Cardiac Myocyte Hypertrophy. . 2023-03-31. Pubmed ID: 36883446; DOI: 10.1161/circresaha.122.321448; PMC: PMC10045983 LUMCi027-ALUMCi027-A-1 2023-03-31 2023-03-31 PubMed: 36883446 DOI: 10.1161/circresaha.122.321448Associated cell lines:
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Liang H, Zhu W, Shen C, Zhu H
Generation of an induced pluripotent stem cell line (FDCHi008-A) from an infant with chronic intestinal pseudo-obstruction
Liang H et al. Generation of an induced pluripotent stem cell line (FDCHi008-A) from an infant with chronic intestinal pseudo-obstruction. . 2023-04-00. Pubmed ID: 36842377; DOI: 10.1016/j.scr.2023.103042 FDCHi008-A 2023-04-00 2023-04-00 PubMed: 36842377 DOI: 10.1016/j.scr.2023.103042Associated cell lines:
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Popescu AS, Butler CA, Allendorf DH, Piers TM, Mallach A, Roewe J, Reinhardt P, Cinti A, Redaelli L, Boudesco C, Pradier L, Pocock JM, Thornton P, Brown GC
Alzheimer's disease-associated R47H TREM2 increases, but wild-type TREM2 decreases, microglial phagocytosis of synaptosomes and neuronal loss
Popescu AS et al. Alzheimer's disease-associated R47H TREM2 increases, but wild-type TREM2 decreases, microglial phagocytosis of synaptosomes and neuronal loss. . 2023-04-00. Pubmed ID: 36480007; DOI: 10.1002/glia.24318; PMC: PMC10952257 BIONi010-CBIONi010-C-17 2023-04-00 2023-04-00 PubMed: 36480007 DOI: 10.1002/glia.24318Associated cell lines:
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Cao S, Guo R, Fu Z, Liu Y, Wu T, Zhou Z, Zhang J, Liu X, Song Y, Ma J
Induced human pluripotent stem cells (HEBHMUi013-A) derived from a patient of sporadic Alzheimer's disease
Cao S et al. Induced human pluripotent stem cells (HEBHMUi013-A) derived from a patient of sporadic Alzheimer's disease. . 2023-04-00. Pubmed ID: 36870256; DOI: 10.1016/j.scr.2023.103052 HEBHMUi001-AHEBHMUi013-A 2023-04-00 2023-04-00 PubMed: 36870256 DOI: 10.1016/j.scr.2023.103052Associated cell lines:
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Feng W, Li C, Li Y, Yang J, Fan R
Generation of an induced pluripotent stem cell line from an aortic dissection patient carrying MCTP2/c.2635T > G mutation
Feng W et al. Generation of an induced pluripotent stem cell line from an aortic dissection patient carrying MCTP2/c.2635T > G mutation. . 2023-04-00. Pubmed ID: 36868039; DOI: 10.1016/j.scr.2023.103058 GDSRMi001-A 2023-04-00 2023-04-00 PubMed: 36868039 DOI: 10.1016/j.scr.2023.103058Associated cell lines:
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Nowak B, Kozlowska E, Pawlik W, Fiszer A
Atrophin-1 Function and Dysfunction in Dentatorubral-Pallidoluysian Atrophy
Nowak B et al. Atrophin-1 Function and Dysfunction in Dentatorubral-Pallidoluysian Atrophy. . 2023-04-00. Pubmed ID: 36809552; DOI: 10.1002/mds.29355 IBCHi001-ACSSi008-A 2023-04-00 2023-04-00 PubMed: 36809552 DOI: 10.1002/mds.29355Associated cell lines:
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Lee H, Price J, Srivastava DP, Thuret S
In vitro characterization on the role of APOE polymorphism in human hippocampal neurogenesis
Lee H et al. In vitro characterization on the role of APOE polymorphism in human hippocampal neurogenesis. . 2023-04-00. Pubmed ID: 36709412; DOI: 10.1002/hipo.23502; PMC: PMC10947111 BIONi010-CBIONi010-C-2BIONi010-C-3BIONi010-C-4BIONi010-C-6 2023-04-00 2023-04-00 PubMed: 36709412 DOI: 10.1002/hipo.23502Associated cell lines:
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Moon HJ, Lee N, Moon JY, Lee JH, Kim JH
Characterization of human induced pluripotent stem cells line (PNUSCRi004-A) from a Parkinson's disease patient carrying L483P, A495P and V499V mutations
Moon HJ et al. Characterization of human induced pluripotent stem cells line (PNUSCRi004-A) from a Parkinson's disease patient carrying L483P, A495P and V499V mutations. . 2023-04-00. Pubmed ID: 36805467; DOI: 10.1016/j.scr.2023.103051 PNUSCRi004-A 2023-04-00 2023-04-00 PubMed: 36805467 DOI: 10.1016/j.scr.2023.103051Associated cell lines:
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Davies KC, Bozaoglu K, Lockhart PJ
Generation and heterozygous repair of human iPSC lines from three individuals with cerebellar ataxia, neuropathy and vestibular areflexia syndrome (CANVAS) carrying biallelic AAGGG expansions in RFC1
Davies KC et al. Generation and heterozygous repair of human iPSC lines from three individuals with cerebellar ataxia, neuropathy and vestibular areflexia syndrome (CANVAS) carrying biallelic AAGGG expansions in RFC1. . 2023-04-00. Pubmed ID: 36805468; DOI: 10.1016/j.scr.2023.103047 MCRIi025-AMCRIi025-BMCRIi026-AMCRIi026-BMCRIi027-AMCRIi027-B 2023-04-00 2023-04-00 PubMed: 36805468 DOI: 10.1016/j.scr.2023.103047Associated cell lines:
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Son N, Son YS, Jung CR, Son MY
Generation of a human fibroblast-derived induced pluripotent stem cell line KRIBBi009-A from a patient with breast cancer
Son N et al. Generation of a human fibroblast-derived induced pluripotent stem cell line KRIBBi009-A from a patient with breast cancer. . 2023-04-00. Pubmed ID: 36925228; DOI: 10.1016/j.scr.2023.103060 KRIBBi009-A 2023-04-00 2023-04-00 PubMed: 36925228 DOI: 10.1016/j.scr.2023.103060Associated cell lines:
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Xu Ping, Chen Zhuolin, Ma Jianchi, Shan Yongli, Wang Yuan, Xie Bingbing, Zheng Dandan, Guo Fuying, Song Xiaojing, Gao Guanjie, Ye Ke, Liu Yizhi, Pan Guangjin, Jiang Bin, Peng Fuhua, Zhong Xiufeng
Biallelic CLCN2 mutations cause retinal degeneration by impairing retinal pigment epithelium phagocytosis and chloride channel function
Xu Ping et al. Biallelic CLCN2 mutations cause retinal degeneration by impairing retinal pigment epithelium phagocytosis and chloride channel function. . 2023-04-00. DOI: 10.1007/s00439-023-02531-7 SKLOi001-A 2023-04-00 2023-04-00 DOI: 10.1007/s00439-023-02531-7Associated cell lines:
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Dyke E, Bijnagte-Schoenmaker C, Wu KM, Oudakker A, Roepman R, Nadif Kasri N
Generation of induced pluripotent stem cell line carrying frameshift variants in NPHP1 (UCSFi001-A-68) using CRISPR/Cas9
Dyke E et al. Generation of induced pluripotent stem cell line carrying frameshift variants in NPHP1 (UCSFi001-A-68) using CRISPR/Cas9. . 2023-04-00. Pubmed ID: 36842376; DOI: 10.1016/j.scr.2023.103053 UCSFi001-AUCSFi001-A-68 2023-04-00 2023-04-00 PubMed: 36842376 DOI: 10.1016/j.scr.2023.103053Associated cell lines:
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Banal C, Quelennec E, Talbotec C, Khiat A, Charbit-Henrion F, Cerf-Bensussan N, Lefort N, Lebreton C
Generation of induced pluripotent stem cells (iPSCs) from a microvillus inclusion disease patient with a homozygous missense mutation in UNC45A
Banal C et al. Generation of induced pluripotent stem cells (iPSCs) from a microvillus inclusion disease patient with a homozygous missense mutation in UNC45A. . 2023-04-00. Pubmed ID: 36868038; DOI: 10.1016/j.scr.2023.103057 IMAGINi004-AIMAGINi005-AIMAGINi013-AIMAGINi020-A 2023-04-00 2023-04-00 PubMed: 36868038 DOI: 10.1016/j.scr.2023.103057Associated cell lines:
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Ham O, Kim S, Lee Y, Lee MO
Generation of telomeric repeat binding factor 1 (TRF1)-knockout human embryonic stem cell lines, KRIBBe010-A-95, KRIBBe010-A-96, and KRIBBe010-A-97, using CRISPR/Cas9 technology
Ham O et al. Generation of telomeric repeat binding factor 1 (TRF1)-knockout human embryonic stem cell lines, KRIBBe010-A-95, KRIBBe010-A-96, and KRIBBe010-A-97, using CRISPR/Cas9 technology. . 2023-04-00. Pubmed ID: 36805322; DOI: 10.1016/j.scr.2023.103045 WAe009-A-95WAe009-A-96WAe009-A-97 2023-04-00 2023-04-00 PubMed: 36805322 DOI: 10.1016/j.scr.2023.103045Associated cell lines:
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Fedorova V, Pospisilova V, Vanova T, Amruz Cerna K, Abaffy P, Sedmik J, Raska J, Vochyanova S, Matusova Z, Houserova J, Valihrach L, Hodny Z, Bohaciakova D
Glioblastoma and cerebral organoids: development and analysis of an in vitro model for glioblastoma migration
Fedorova V et al. Glioblastoma and cerebral organoids: development and analysis of an in vitro model for glioblastoma migration. . 2023-04-00. Pubmed ID: 36744875; DOI: 10.1002/1878-0261.13389; PMC: PMC10061278 MUNIi008-AMUNIi009-AMUNIi010-A 2023-04-00 2023-04-00 PubMed: 36744875 DOI: 10.1002/1878-0261.13389Associated cell lines:
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Stępniewski J, Jeż M, Dulak J
Generation of miR-15a/16-1 cluster-deficient human induced pluripotent stem cell line (DMBi001-A-2) using CRISPR/Cas9 gene editing
Stępniewski J et al. Generation of miR-15a/16-1 cluster-deficient human induced pluripotent stem cell line (DMBi001-A-2) using CRISPR/Cas9 gene editing. . 2023-04-00. Pubmed ID: 36801567; DOI: 10.1016/j.scr.2023.103046 DMBi001-ADMBi001-A-2 2023-04-00 2023-04-00 PubMed: 36801567 DOI: 10.1016/j.scr.2023.103046Associated cell lines:
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Chen L, Wang J, Yang T, Xie L, Cui Z, Yu Q, Zhong J, Chan HF, Xue Y, Guo Y, Chen J
Establishment of iPS cell line (KLRMMEi003-A) from a patient with Usher syndrome due to USH2A mutation
Chen L et al. Establishment of iPS cell line (KLRMMEi003-A) from a patient with Usher syndrome due to USH2A mutation. . 2023-04-00. Pubmed ID: 36863132; DOI: 10.1016/j.scr.2023.103055 KLRMMEi003-A 2023-04-00 2023-04-00 PubMed: 36863132 DOI: 10.1016/j.scr.2023.103055Associated cell lines:
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Cohen PJR, Luquet E, Pletenka J, Leonard A, Warter E, Gurchenkov B, Carrere J, Rieu C, Hardouin J, Moncaubeig F, Lanero M, Quelennec E, Wurtz H, Jamet E, Demarco M, Banal C, Van Liedekerke P, Nassoy P, Feyeux M, Lefort N, Alessandri K
Engineering 3D micro-compartments for highly efficient and scale-independent expansion of human pluripotent stem cells in bioreactors
Cohen PJR et al. Engineering 3D micro-compartments for highly efficient and scale-independent expansion of human pluripotent stem cells in bioreactors. . 2023-04-00. Pubmed ID: 36764194; DOI: 10.1016/j.biomaterials.2023.122033 IMAGINi004-AIMAGINi005-A 2023-04-00 2023-04-00 PubMed: 36764194 DOI: 10.1016/j.biomaterials.2023.122033Associated cell lines:
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Dursun FE, Özen F
SMPD1 gene variants in patients with β-Thalassemia major
Dursun FE et al. SMPD1 gene variants in patients with β-Thalassemia major. . 2023-04-00. Pubmed ID: 36725747; DOI: 10.1007/s11033-023-08275-x; PMC: PMC10042979 TRNDi009-C 2023-04-00 2023-04-00 PubMed: 36725747 DOI: 10.1007/s11033-023-08275-xAssociated cell lines:
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Kim IG, Jung WH, You G, Lee H, Shin YJ, Lim SW, Chung BH, Mok H
Efficient Delivery of Globotriaosylceramide Synthase siRNA using Polyhistidine-Incorporated Lipid Nanoparticles
Kim IG et al. Efficient Delivery of Globotriaosylceramide Synthase siRNA using Polyhistidine-Incorporated Lipid Nanoparticles. . 2023-04-00. Pubmed ID: 36728673; DOI: 10.1002/mabi.202200423 CMCi006-ACMCi007-A 2023-04-00 2023-04-00 PubMed: 36728673 DOI: 10.1002/mabi.202200423 -
Llach Pou M, Thiberge C, Van der Zwan M, Devi Govindan A, Pons S, Maskos U, Cloëz-Tayarani I
Developmental Changes of Human Neural Progenitor Cells Grafted into the Ventricular System and Prefrontal Cortex of Mouse Brain in Utero
Llach Pou M et al. Developmental Changes of Human Neural Progenitor Cells Grafted into the Ventricular System and Prefrontal Cortex of Mouse Brain in Utero. . 2023-03-31. Pubmed ID: 37048140; DOI: 10.3390/cells12071067; PMC: PMC10093207 WTSIi002-A 2023-03-31 2023-03-31 PubMed: 37048140 DOI: 10.3390/cells12071067Associated cell lines:
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Liu Y, Jin Y, Chen T, Wu Y, Peng X, Li W, Wei S, Chen M, Zou Q, Guo S, Xu J, Tang C, Zhou X
Retraction notice to "Generation of a homozygous ARHGAP11B knockout hiPSC line by CRISPR/Cas9 system" <[Stem Cell Res. 61 (2022) 102764]>
Liu Y et al. Retraction notice to "Generation of a homozygous ARHGAP11B knockout hiPSC line by CRISPR/Cas9 system" <[Stem Cell Res. 61 (2022) 102764]>. . 2023-04-00. Pubmed ID: 36868040; DOI: 10.1016/j.scr.2023.103021 WYUi001-A 2023-04-00 2023-04-00 PubMed: 36868040 DOI: 10.1016/j.scr.2023.103021Associated cell lines:
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Li C, Dong X, Lin Y, Sun X, Cai L, Yang X, Cui Y, Qin L, Wang J
Establishing a human embryonic stem cell line (SKLRMe005-A) from a blastocyst with congenital heart disease (CHD)
Li C et al. Establishing a human embryonic stem cell line (SKLRMe005-A) from a blastocyst with congenital heart disease (CHD). . 2023-04-00. Pubmed ID: 36805323; DOI: 10.1016/j.scr.2023.103049 SKLRMe005-A 2023-04-00 2023-04-00 PubMed: 36805323 DOI: 10.1016/j.scr.2023.103049Associated cell lines:
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Sidhaye J, Trepte P, Sepke N, Novatchkova M, Schutzbier M, Dürnberger G, Mechtler K, Knoblich JA
Integrated transcriptome and proteome analysis reveals posttranscriptional regulation of ribosomal genes in human brain organoids
Sidhaye J et al. Integrated transcriptome and proteome analysis reveals posttranscriptional regulation of ribosomal genes in human brain organoids. . 2023-03-29. Pubmed ID: 36989136; DOI: 10.7554/elife.85135; PMC: PMC10059687 WTSIi015-A 2023-03-29 2023-03-29 PubMed: 36989136 DOI: 10.7554/elife.85135Associated cell lines:
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Shtykalova Sofia, Deviatkin Dmitriy, Freund Svetlana, Egorova Anna, Kiselev Anton
Non-Viral Carriers for Nucleic Acids Delivery: Fundamentals and Current Applications
Shtykalova Sofia et al. Non-Viral Carriers for Nucleic Acids Delivery: Fundamentals and Current Applications. . 2023-03-29. DOI: 10.3390/life13040903 USTCi001-A 2023-03-29 2023-03-29 DOI: 10.3390/life13040903Associated cell lines:
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Kermani F, Mosqueira M, Peters K, Lemma ED, Rapti K, Grimm D, Bastmeyer M, Laugsch M, Hecker M, Ullrich ND
Membrane remodelling triggers maturation of excitation-contraction coupling in 3D-shaped human-induced pluripotent stem cell-derived cardiomyocytes
Kermani F et al. Membrane remodelling triggers maturation of excitation-contraction coupling in 3D-shaped human-induced pluripotent stem cell-derived cardiomyocytes. . 2023-03-29. Pubmed ID: 36988697; DOI: 10.1007/s00395-023-00984-5; PMC: PMC10060306 UMGi014-C 2023-03-29 2023-03-29 PubMed: 36988697 DOI: 10.1007/s00395-023-00984-5Associated cell lines:
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Jassim Tabarak Sabah, Ali Rusul Waleed, Jaber Nawar Rushdi
Expression and genetic polymorphism of Foxp3 gene and its association to breast cancer susceptibility
Jassim Tabarak Sabah et al. Expression and genetic polymorphism of Foxp3 gene and its association to breast cancer susceptibility. . 2023-03-28. DOI: 10.51248/.v43i01.2531 PUMCi001-A 2023-03-28 2023-03-28 DOI: 10.51248/.v43i01.2531Associated cell lines:
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Astro Veronica, Fiacco Elisabetta, Cardona-Londoño Kelly Johanna, De Toma Ilario, Alzahrani Hams Saeed, Alama Jumana, Kokandi Amal, Hamoda Taha Abo-Almagd Abdel-Meguid, Felemban Majed, Adamo Antonio
A transcriptomic signature of X chromosome overdosage in Saudi Klinefelter syndrome induced pluripotent stem cells
Astro Veronica et al. A transcriptomic signature of X chromosome overdosage in Saudi Klinefelter syndrome induced pluripotent stem cells. . 2023-03-27. DOI: 10.1530/ec-22-0515 KAUSTi001-AKAUSTi003-AKAUSTi004-AKAUSTi004-BKAUSTi005-AKAUSTi005-BKAUSTi005-CKAUSTi001-BKAUSTi006-AKAUSTi006-BKAUSTi007-AKAUSTi008-AKAUSTi008-BKAUSTi008-CKAUSTi008-DKAUSTi008-EKAUSTi008-FKAUSTi008-GKAUSTi007-BKAUSTi009-AKAUSTi009-BKAUSTi010-AKAUSTi010-B 2023-03-27 2023-03-27 DOI: 10.1530/ec-22-0515 -
Demchenko Anna, Kondrateva Ekaterina, Tabakov Vyacheslav, Efremova Anna, Salikhova Diana, Bukharova Tatiana, Goldshtein Dmitry, Balyasin Maxim, Bulatenko Natalia, Amelina Elena, Lavrov Alexander, Smirnikhina Svetlana
Airway and Lung Organoids from Human-Induced Pluripotent Stem Cells Can Be Used to Assess CFTR Conductance
Demchenko Anna et al. Airway and Lung Organoids from Human-Induced Pluripotent Stem Cells Can Be Used to Assess CFTR Conductance. . 2023-03-27. DOI: 10.3390/ijms24076293 RCMGi001-ARCMGi002-ARCMGi004-ARCMGi005-ARCMGi008-A 2023-03-27 2023-03-27 DOI: 10.3390/ijms24076293Associated cell lines:
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Lamolda M, Frejo L, Gallego-Martinez A, Lopez-Escamez JA
Application of Human Stem Cells to Model Genetic Sensorineural Hearing Loss and Meniere Disease
Lamolda M et al. Application of Human Stem Cells to Model Genetic Sensorineural Hearing Loss and Meniere Disease. . 2023-03-23. Pubmed ID: 37048061; DOI: 10.3390/cells12070988; PMC: PMC10093542 GENYOi005-AGENYOi007-A 2023-03-23 2023-03-23 PubMed: 37048061 DOI: 10.3390/cells12070988Associated cell lines:
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Tsui Hoyee, van Kampen Sebastiaan Johannes, Han Su Ji, Meraviglia Viviana, van Ham Willem B., Casini Simona, van der Kraak Petra, Vink Aryan, Yin Xiaoke, Mayr Manuel, Bossu Alexandre, Marchal Gerard A., Monshouwer-Kloots Jantine, Eding Joep, Versteeg Danielle, de Ruiter Hesther, Bezstarosti Karel, Groeneweg Judith, Klaasen Sjoerd J., van Laake Linda W., Demmers Jeroen A.A., Kops Geert J.P.L., Mummery Christine L., van Veen Toon A.B., Remme Carol Ann, Bellin Milena, van Rooij Eva
Desmosomal protein degradation as an underlying cause of arrhythmogenic cardiomyopathy
Tsui Hoyee et al. Desmosomal protein degradation as an underlying cause of arrhythmogenic cardiomyopathy. . 2023-03-22. DOI: 10.1126/scitranslmed.add4248 LUMCi027-A 2023-03-22 2023-03-22 DOI: 10.1126/scitranslmed.add4248Associated cell lines:
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Du Hongmei, Huo Zijun, Chen Yanchun, Zhao Zhenhan, Meng Fandi, Wang Xuemei, Liu Shiyue, Zhang Haoyun, Zhou Fenghua, Liu Jinmeng, Zhang Lingyun, Zhou Shuanhu, Guan Yingjun, Wang Xin
Induced Pluripotent Stem Cells and Their Applications in Amyotrophic Lateral Sclerosis
Du Hongmei et al. Induced Pluripotent Stem Cells and Their Applications in Amyotrophic Lateral Sclerosis. . 2023-03-22. DOI: 10.3390/cells12060971 ZZUi034-A 2023-03-22 2023-03-22 DOI: 10.3390/cells12060971Associated cell lines:
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Perez-Sanchez Jimena, Middleton Steven J., Pattison Luke A., Hilton Helen, Awadelkareem Mosab Ali, Zuberi Sana R., Renke Maria B., Hu Huimin, Yang Xun, Clark Alex J., St Ewan, Smith John, Bennett David L.
Inhibition of sensory neuron driven acute, inflammatory, and neuropathic pain using a humanised chemogenetic system
Perez-Sanchez Jimena et al. Inhibition of sensory neuron driven acute, inflammatory, and neuropathic pain using a humanised chemogenetic system. . 2023-03-21. DOI: 10.1101/2023.03.21.533690 RCi002-A 2023-03-21 2023-03-21 DOI: 10.1101/2023.03.21.533690Associated cell lines:
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Cavestro Chiara, Diodato Daria, Tiranti Valeria, Di Meo Ivano
Inherited Disorders of Coenzyme A Biosynthesis: Models, Mechanisms, and Treatments
Cavestro Chiara et al. Inherited Disorders of Coenzyme A Biosynthesis: Models, Mechanisms, and Treatments. . 2023-03-21. DOI: 10.3390/ijms24065951 MRIi028-AHMGUi003-A 2023-03-21 2023-03-21 DOI: 10.3390/ijms24065951Associated cell lines:
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Zhong Kun, Shi Haijie, Wu Wenli, Xu Haizhu, Wang Hui, Zhao Zhendong
Genotypic spectrum of α-thalassemia and β-thalassemia in newborns of the Li minority in Hainan province, China
Zhong Kun et al. Genotypic spectrum of α-thalassemia and β-thalassemia in newborns of the Li minority in Hainan province, China. . 2023-03-20. DOI: 10.3389/fped.2023.1139387 HNMUi002-AHNMUi003-AHNMUi004-AHNMUi005-AHNMUi006-AHNMUi007-AHNMUi008-AHNMUi009-AHNMUi010-A 2023-03-20 2023-03-20 DOI: 10.3389/fped.2023.1139387Associated cell lines:
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Zhang X, Zhang C, Zhou D, Zhang T, Chen X, Ren J, He C, Meng F, Zhou Q, Yang Q, Dai C, Lin G, Zeng S, Leng L
Telomeres cooperate in zygotic genome activation by affecting DUX4/Dux transcription
Zhang X et al. Telomeres cooperate in zygotic genome activation by affecting DUX4/Dux transcription. . 2023-03-17. Pubmed ID: 36843839; DOI: 10.1016/j.isci.2023.106158; PMC: PMC9950522 NERCe003-ANERCe003-A-3 2023-03-17 2023-03-17 PubMed: 36843839 DOI: 10.1016/j.isci.2023.106158Associated cell lines:
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von der Bey M, De Cicco S, Zach S, Hengerer B, Ercan-Herbst E
Three-dimensional co-culture platform of human induced pluripotent stem cell-derived oligodendrocyte lineage cells and neurons for studying myelination
von der Bey M et al. Three-dimensional co-culture platform of human induced pluripotent stem cell-derived oligodendrocyte lineage cells and neurons for studying myelination. . 2023-03-17. Pubmed ID: 36933222; DOI: 10.1016/j.xpro.2023.102164; PMC: PMC10034497 STBCi102-A 2023-03-17 2023-03-17 PubMed: 36933222 DOI: 10.1016/j.xpro.2023.102164Associated cell lines:
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Bantounas Ioannis, Rooney Kirsty M., Lopes Filipa M., Tengku Faris, Woods Steven, Zeef Leo A. H., Kuba Shweta Y., Bates Nicola, Hummelgaard Sandra, Hillman Katherine A, Cereghini Silvia, Woolf Adrian S., Kimber Susan J.
Human pluripotent stem cell-derived kidney organoids reveal tubular epithelial pathobiology of heterozygousHNF1B-associated dysplastic kidney malformations
Bantounas Ioannis et al. Human pluripotent stem cell-derived kidney organoids reveal tubular epithelial pathobiology of heterozygousHNF1B-associated dysplastic kidney malformations. . 2023-03-15. DOI: 10.1101/2023.03.14.532598 UMANe002-A-4UMANe002-A-5UMANCi001-AUMANCi002-AUMANCi003-A 2023-03-15 2023-03-15 DOI: 10.1101/2023.03.14.532598Associated cell lines:
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Richard D, Pregizer S, Venkatasubramanian D, Raftery RM, Muthuirulan P, Liu Z, Capellini TD, Craft AM
Lineage-specific differences and regulatory networks governing human chondrocyte development
Richard D et al. Lineage-specific differences and regulatory networks governing human chondrocyte development. . 2023-03-15. Pubmed ID: 36920035; DOI: 10.7554/elife.79925; PMC: PMC10069868 WAe009-A 2023-03-15 2023-03-15 PubMed: 36920035 DOI: 10.7554/elife.79925Associated cell lines:
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Gartz M, Haberman M, Sutton J, Slick RA, Luttrell SM, Mack DL, Lawlor MW
ACTA1 H40Y mutant iPSC-derived skeletal myocytes display mitochondrial defects in an in vitro model of nemaline myopathy
Gartz M et al. ACTA1 H40Y mutant iPSC-derived skeletal myocytes display mitochondrial defects in an in vitro model of nemaline myopathy. . 2023-03-15. Pubmed ID: 36796746; DOI: 10.1016/j.yexcr.2023.113507; PMC: PMC9993434 SDQLCHi004-ASDQLCHi017-A 2023-03-15 2023-03-15 PubMed: 36796746 DOI: 10.1016/j.yexcr.2023.113507Associated cell lines:
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Somogyi A, Kirkham ED, Lloyd-Evans E, Winston J, Allen ND, Mackrill JJ, Anderson KE, Hawkins PT, Gardiner SE, Waller-Evans H, Sims R, Boland B, O'Neill C
The synthetic TRPML1 agonist ML-SA1 rescues Alzheimer-related alterations of the endosomal-autophagic-lysosomal system
Somogyi A et al. The synthetic TRPML1 agonist ML-SA1 rescues Alzheimer-related alterations of the endosomal-autophagic-lysosomal system. . 2023-03-15. Pubmed ID: 36825945; DOI: 10.1242/jcs.259875; PMC: PMC10112969 BIONi010-CBIONi010-C-2BIONi010-C-3BIONi010-C-4BIONi010-C-6 2023-03-15 2023-03-15 PubMed: 36825945 DOI: 10.1242/jcs.259875Associated cell lines:
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Zhu Q, Mishra A, Park JS, Liu D, Le DT, Gonzalez SZ, Anderson-Crannage M, Park JM, Park GH, Tarbay L, Daneshvar K, Brandenburg M, Signoretti C, Zinski A, Gardner EJ, Zheng KL, Abani CP, Hu C, Beaudreault CP, Zhang XL, Stanton PK, Cho JH, Velíšek L, Velíšková J, Javed S, Leonard CS, Kim HY, Chung S
Human cortical interneurons optimized for grafting specifically integrate, abort seizures, and display prolonged efficacy without over-inhibition
Zhu Q et al. Human cortical interneurons optimized for grafting specifically integrate, abort seizures, and display prolonged efficacy without over-inhibition. . 2023-03-15. Pubmed ID: 36626901; DOI: 10.1016/j.neuron.2022.12.014; PMC: PMC10023356 WAe009-A 2023-03-15 2023-03-15 PubMed: 36626901 DOI: 10.1016/j.neuron.2022.12.014Associated cell lines:
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Ritzau-Jost A, Nerlich J, Kaas T, Krueger M, Tsintsadze T, Eilers J, Barbour B, Smith SM, Hallermann S
Direct whole-cell patch-clamp recordings from small boutons in rodent primary neocortical neuron cultures
Ritzau-Jost A et al. Direct whole-cell patch-clamp recordings from small boutons in rodent primary neocortical neuron cultures. . 2023-03-14. Pubmed ID: 36920913; DOI: 10.1016/j.xpro.2023.102168; PMC: PMC10026040 BIHi005-ABIHi005-A-24 2023-03-14 2023-03-14 PubMed: 36920913 DOI: 10.1016/j.xpro.2023.102168Associated cell lines:
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Müthel S, Marg A, Ignak B, Kieshauer J, Escobar H, Stadelmann C, Spuler S
Cas9-induced single cut enables highly efficient and template-free repair of a muscular dystrophy causing founder mutation
Müthel S et al. Cas9-induced single cut enables highly efficient and template-free repair of a muscular dystrophy causing founder mutation. . 2023-03-14. Pubmed ID: 36865086; DOI: 10.1016/j.omtn.2023.02.005; PMC: PMC9972404 MDCi011-AMDCi011-BMDCi012-AMDCi012-BMDCi013-AMDCi013-B 2023-03-14 2023-03-14 PubMed: 36865086 DOI: 10.1016/j.omtn.2023.02.005 -
Huang Z, Powell R, Kankowski S, Phillips JB, Haastert-Talini K
Culture Conditions for Human Induced Pluripotent Stem Cell-Derived Schwann Cells: A Two-Centre Study
Huang Z et al. Culture Conditions for Human Induced Pluripotent Stem Cell-Derived Schwann Cells: A Two-Centre Study. . 2023-03-10. Pubmed ID: 36982441; DOI: 10.3390/ijms24065366; PMC: PMC10049204 MHHi001-A 2023-03-10 2023-03-10 PubMed: 36982441 DOI: 10.3390/ijms24065366Associated cell lines:
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Pavlou S, Foskolou S, Patikas N, Field SF, Papachristou EK, Santos C, Edwards AR, Kishore K, Ansari R, Rajan SS, Fernandes HJR, Metzakopian E
CRISPR-Cas9 genetic screen leads to the discovery of L-Moses, a KAT2B inhibitor that attenuates Tunicamycin-mediated neuronal cell death
Pavlou S et al. CRISPR-Cas9 genetic screen leads to the discovery of L-Moses, a KAT2B inhibitor that attenuates Tunicamycin-mediated neuronal cell death. . 2023-03-09. Pubmed ID: 36894612; DOI: 10.1038/s41598-023-31141-6; PMC: PMC9998435 CAMi014-A 2023-03-09 2023-03-09 PubMed: 36894612 DOI: 10.1038/s41598-023-31141-6Associated cell lines:
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van Amerongen RA, Morton LT, Chaudhari UG, Remst DFG, Hagedoorn RS, van den Berg CW, Freund C, Falkenburg JHF, Heemskerk MHM
Human iPSC-derived preclinical models to identify toxicity of tumor-specific T cells with clinical potential
van Amerongen RA et al. Human iPSC-derived preclinical models to identify toxicity of tumor-specific T cells with clinical potential. . 2023-03-09. Pubmed ID: 36816758; DOI: 10.1016/j.omtm.2023.01.005; PMC: PMC9931760 LUMCi028-ALUMCi029-ALUMCi004-B 2023-03-09 2023-03-09 PubMed: 36816758 DOI: 10.1016/j.omtm.2023.01.005Associated cell lines:
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Bressan E, Reed X, Bansal V, Hutchins E, Cobb MM, Webb MG, Alsop E, Grenn FP, Illarionova A, Savytska N, Violich I, Broeer S, Fernandes N, Sivakumar R, Beilina A, Billingsley KJ, Berghausen J, Pantazis CB, Pitz V, Patel D, Daida K, Meechoovet B, Reiman R, Courtright-Lim A, Logemann A, Antone J, Barch M, Kitchen R, Li Y, Dalgard CL, American Genome Center, Rizzu P, Hernandez DG, Hjelm BE, Nalls M, Gibbs JR, Finkbeiner S, Cookson MR, Van Keuren-Jensen K, Craig DW, Singleton AB, Heutink P, Blauwendraat C
The Foundational Data Initiative for Parkinson Disease: Enabling efficient translation from genetic maps to mechanism
Bressan E et al. The Foundational Data Initiative for Parkinson Disease: Enabling efficient translation from genetic maps to mechanism. . 2023-03-08. Pubmed ID: 36950378; DOI: 10.1016/j.xgen.2023.100261; PMC: PMC10025424 CDIi013-ACDIi014-ACDIi015-ACDIi016-ACDIi017-ACDIi018-ACDIi019-ACDIi020-ACDIi021-ACDIi022-ACDIi023-ACDIi024-ACDIi025-ACDIi026-ACDIi027-ACDIi028-ACDIi029-ACDIi030-ACDIi031-ACDIi032-ACDIi033-ACDIi034-ACDIi035-ACDIi036-ACDIi037-ACDIi038-ACDIi039-ACDIi040-ACDIi041-ACDIi042-ACDIi043-ACDIi044-ACDIi045-ACDIi046-ACDIi047-ACDIi048-ACDIi049-ACDIi050-ACDIi051-ACDIi052-ACDIi053-ACDIi054-ACDIi055-ACDIi056-ACDIi057-ACDIi058-ACDIi059-ACDIi060-ACDIi061-ACDIi062-ACDIi063-ACDIi064-ACDIi065-ACDIi066-ACDIi067-ACDIi068-ACDIi069-ACDIi070-ACDIi071-ACDIi072-ACDIi073-ACDIi074-ACDIi075-ACDIi076-ACDIi077-ACDIi078-ACDIi079-ACDIi080-ACDIi081-ACDIi082-ACDIi083-ACDIi084-ACDIi085-ACDIi086-ACDIi087-ACDIi088-ACDIi089-ACDIi090-ACDIi091-ACDIi092-ACDIi093-ACDIi094-ACDIi095-ACDIi096-ACDIi097-ACDIi098-ACDIi099-ACDIi100-ACDIi101-ACDIi102-ACDIi103-ACDIi104-ACDIi105-A 2023-03-08 2023-03-08 PubMed: 36950378 DOI: 10.1016/j.xgen.2023.100261 -
Cao X, Mircea M, Yakala GK, van den Hil FE, Brescia M, Mei H, Mummery CL, Semrau S, Orlova VV
ETV2 Upregulation Marks the Specification of Early Cardiomyocytes and Endothelial Cells During Co-differentiation
Cao X et al. ETV2 Upregulation Marks the Specification of Early Cardiomyocytes and Endothelial Cells During Co-differentiation. . 2023-03-02. Pubmed ID: 36512477; DOI: 10.1093/stmcls/sxac086; PMC: PMC9982073 CRMi003-ALUMCi028-A 2023-03-02 2023-03-02 PubMed: 36512477 DOI: 10.1093/stmcls/sxac086Associated cell lines:
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Do Quyen B., Ng Bryan, Gomez Ricardo Marquez, Beccano-Kelly Dayne, Ibarra-Aizpura Naroa, Caiazza Maria-Claudia, Lang Charmaine, Baleriola Jimena, Bengoa-Vergniory Nora, Wade-Martins Richard
Early striatal hyperexcitability in anin vitrohuman striatal microcircuit model carrying the Parkinson’sGBA-N370Smutation
Do Quyen B. et al. Early striatal hyperexcitability in anin vitrohuman striatal microcircuit model carrying the Parkinson’sGBA-N370Smutation. . 2023-03-02. DOI: 10.1101/2023.03.01.530566 UOXFi001-BUOXFi003-ASTBCi101-A 2023-03-02 2023-03-02 DOI: 10.1101/2023.03.01.530566Associated cell lines:
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Chiba Kyoko, Kita Tomoki, Anazawa Yuzu, Niwa Shinsuke
Insight into the regulation of axonal transport from the study of KIF1A-associated neurological disorder
Chiba Kyoko et al. Insight into the regulation of axonal transport from the study of KIF1A-associated neurological disorder. . 2023-03-01. DOI: 10.1242/jcs.260742 SDUBMSi001-A 2023-03-01 2023-03-01 DOI: 10.1242/jcs.260742Associated cell lines:
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Chou CW, Hsu YC
Current development of patient-specific induced pluripotent stem cells harbouring mitochondrial gene mutations and their applications in the treatment of sensorineural hearing loss
Chou CW et al. Current development of patient-specific induced pluripotent stem cells harbouring mitochondrial gene mutations and their applications in the treatment of sensorineural hearing loss. . 2023-03-01. Pubmed ID: 36649664; DOI: 10.1016/j.heares.2023.108689 FINCBi001-AMMCi001-A 2023-03-01 2023-03-01 PubMed: 36649664 DOI: 10.1016/j.heares.2023.108689Associated cell lines:
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Okura S, Ishii H, Suzuki A, Saegusa C, Fujiki K, Sugano K, Suzuki N, Saeki T, Matsuzaki S, Ozawa H, Fujioka M, Hosoya M, Okano H
Generation of two induced pluripotent stem cell lines from individuals without auditory disorders
Okura S et al. Generation of two induced pluripotent stem cell lines from individuals without auditory disorders. . 2023-03-00. Pubmed ID: 36630839; DOI: 10.1016/j.scr.2023.103017 KEIUi002-AKEIUi003-A 2023-03-00 2023-03-00 PubMed: 36630839 DOI: 10.1016/j.scr.2023.103017Associated cell lines:
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Henke MT, Zink A, Diecke S, Prigione A, Schuelke M
Generation of two mother-child pairs of iPSCs from maternally inherited Leigh syndrome patients with m.8993 T > G and m.9176 T > G MT-ATP6 mutations
Henke MT et al. Generation of two mother-child pairs of iPSCs from maternally inherited Leigh syndrome patients with m.8993 T > G and m.9176 T > G MT-ATP6 mutations. . 2023-03-00. Pubmed ID: 36669241; DOI: 10.1016/j.scr.2023.103030 BIHi002-ABIHi266-ABIHi267-BBIHi269-BBIHi276-A 2023-03-00 2023-03-00 PubMed: 36669241 DOI: 10.1016/j.scr.2023.103030 -
Gopurappilly R, Musthafa T, Sukumaran S, Viswanath B, Hasan G
Generation of feeder-independent transgene-free iPSC lines from a young-onset Parkinson's disease (YOPD) patient with a homozygous PLA2G6: c.2222G>A (p. Arg741Gln) mutation (NCBSi003-A) and unaffected heterozygous parent (NCBSi004-A)
Gopurappilly R et al. Generation of feeder-independent transgene-free iPSC lines from a young-onset Parkinson's disease (YOPD) patient with a homozygous PLA2G6: c.2222G>A (p. Arg741Gln) mutation (NCBSi003-A) and unaffected heterozygous parent (NCBSi004-A). . 2023-03-00. Pubmed ID: 36706537; DOI: 10.1016/j.scr.2023.103033; PMC: PMC7614486 NCBSi003-ANCBSi004-A 2023-03-00 2023-03-00 PubMed: 36706537 DOI: 10.1016/j.scr.2023.103033Associated cell lines:
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Ding T, Gao Z, Liu H, Li Y, Liu S, Jian L
Establishment of a PPP2CA homozygous knockout human embryonic stem cell line via CRISPR/Cas9 system
Ding T et al. Establishment of a PPP2CA homozygous knockout human embryonic stem cell line via CRISPR/Cas9 system. . 2023-03-00. Pubmed ID: 36724553; DOI: 10.1016/j.scr.2023.103029 WAe009-AWAe009-A-25WAe009-A-36WAe009-A-C 2023-03-00 2023-03-00 PubMed: 36724553 DOI: 10.1016/j.scr.2023.103029Associated cell lines:
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Kaewboonlert N, Wattanapanitch M, Praditsap O, Deejai N, Chanprasert C, Sawasdee N, Nettuwakul C, Wanachiwanawin W, Sritippayawan S, Thamtarana PJ, Yenchitsomanus PT, Rungroj N
An induced pluripotent stem cell line (MUSIi019-A) generated from a patient with distal renal tubular acidosis carrying a compound heterozygous mutation in solute carrier family 4 member 1 (SLC4A1) gene
Kaewboonlert N et al. An induced pluripotent stem cell line (MUSIi019-A) generated from a patient with distal renal tubular acidosis carrying a compound heterozygous mutation in solute carrier family 4 member 1 (SLC4A1) gene. . 2023-03-00. Pubmed ID: 36791635; DOI: 10.1016/j.scr.2023.103043 MUSIi019-A 2023-03-00 2023-03-00 PubMed: 36791635 DOI: 10.1016/j.scr.2023.103043Associated cell lines:
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Jeon SB, Kim H, Chun KH, Oh J, Kwon C, Choi HK, Kim S, Kim HP, Kim IC, Yoo JY, Park SW, Kang SM, Lee SH
Human induced pluripotent stem cell line YCMi007-A generated from a dilated cardiomyopathy patient with a heterozygous dominant c.613C > T (p. Arg205Trp) variant of the TNNT2 gene
Jeon SB et al. Human induced pluripotent stem cell line YCMi007-A generated from a dilated cardiomyopathy patient with a heterozygous dominant c.613C > T (p. Arg205Trp) variant of the TNNT2 gene. . 2023-03-00. Pubmed ID: 36801602; DOI: 10.1016/j.scr.2023.103048 YCMi007-A 2023-03-00 2023-03-00 PubMed: 36801602 DOI: 10.1016/j.scr.2023.103048Associated cell lines:
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Li Y, Dinkel H, Pakalniskyte D, Busley AV, Cyganek L, Zhong R, Zhang F, Xu Q, Maywald L, Aweimer A, Huang M, Liao Z, Meng Z, Yan C, Prädel T, Rose L, Moscu-Gregor A, Hohn A, Yang Z, Qiao L, Mügge A, Zhou X, Akin I, El-Battrawy I
Novel insights in the pathomechanism of Brugada syndrome and fever-related type 1 ECG changes in a preclinical study using human-induced pluripotent stem cell-derived cardiomyocytes
Li Y et al. Novel insights in the pathomechanism of Brugada syndrome and fever-related type 1 ECG changes in a preclinical study using human-induced pluripotent stem cell-derived cardiomyocytes. . 2023-03-00. Pubmed ID: 36881552; DOI: 10.1002/ctm2.1130; PMC: PMC9990896 UMGi127-AUMGi014-BUMGi130-A 2023-03-00 2023-03-00 PubMed: 36881552 DOI: 10.1002/ctm2.1130 -
Diouf D, Vitale MR, Zöller JEM, Pineau AM, Klopocki E, Hamann C, Ziegler GC, Vanmierlo T, Van den Hove D, Lesch KP
Generation of a ST3GAL3 null mutant induced pluripotent stem cell (iPSC) line (UKWMPi002-A-3) by CRISPR/Cas9 genome editing
Diouf D et al. Generation of a ST3GAL3 null mutant induced pluripotent stem cell (iPSC) line (UKWMPi002-A-3) by CRISPR/Cas9 genome editing. . 2023-03-00. Pubmed ID: 36746102; DOI: 10.1016/j.scr.2023.103038 UKWMPi002-AUKWMPi002-A-3 2023-03-00 2023-03-00 PubMed: 36746102 DOI: 10.1016/j.scr.2023.103038Associated cell lines:
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Arendzen CH, Cramer SJ, Freund CMAH, Mummery CL, Ranga A, Mikkers HMM
Introduction of a Geminin mScarlet Reporter into H2B-mTurq2 hiPSCs for Live-cell Imaging of Proliferation and Cell Cycling
Arendzen CH et al. Introduction of a Geminin mScarlet Reporter into H2B-mTurq2 hiPSCs for Live-cell Imaging of Proliferation and Cell Cycling. . 2023-03-00. Pubmed ID: 36702081; DOI: 10.1016/j.scr.2023.103031 CRMi003-A-2CRMi003-A-3 2023-03-00 2023-03-00 PubMed: 36702081 DOI: 10.1016/j.scr.2023.103031Associated cell lines:
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Yammine KM, Mirda Abularach S, Sampurno L, Bateman JF, Lamandé SR, Shoulders MD
Using CRISPR/Cas9 to generate a heterozygous COL2A1 p.R719C iPSC line (MCRIi019-A-6) model of human precocious osteoarthritis
Yammine KM et al. Using CRISPR/Cas9 to generate a heterozygous COL2A1 p.R719C iPSC line (MCRIi019-A-6) model of human precocious osteoarthritis. . 2023-03-00. Pubmed ID: 36682125; DOI: 10.1016/j.scr.2023.103020; PMC: PMC10038005 MCRIi019-AMCRIi019-A-2MCRIi019-A-5MCRIi019-A-6 2023-03-00 2023-03-00 PubMed: 36682125 DOI: 10.1016/j.scr.2023.103020Associated cell lines:
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Celegato M, Sturlese M, Vasconcelos Costa V, Trevisan M, Lallo Dias AS, Souza Passos IB, Queiroz-Junior CM, Messa L, Favaro A, Moro S, Teixeira MM, Loregian A, Mercorelli B
Small-Molecule Inhibitor of Flaviviral NS3-NS5 Interaction with Broad-Spectrum Activity and Efficacy In Vivo
Celegato M et al. Small-Molecule Inhibitor of Flaviviral NS3-NS5 Interaction with Broad-Spectrum Activity and Efficacy In Vivo. . 2023-02-28. Pubmed ID: 36622141; DOI: 10.1128/mbio.03097-22; PMC: PMC9973282 UNIPDi007-A 2023-02-28 2023-02-28 PubMed: 36622141 DOI: 10.1128/mbio.03097-22Associated cell lines:
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Aalders J, Léger L, Demolder A, Muiño Mosquera L, Coucke P, Menten B, De Backer J, van Hengel J
Generation of human induced pluripotent stem cell line UGENTi001-A from a patient with Marfan syndrome carrying a heterozygous c.7754 T > C variant in FBN1 and the isogenic control UGENT001-A-1 using CRISPR/Cas9 editing
Aalders J et al. Generation of human induced pluripotent stem cell line UGENTi001-A from a patient with Marfan syndrome carrying a heterozygous c.7754 T > C variant in FBN1 and the isogenic control UGENT001-A-1 using CRISPR/Cas9 editing. . 2023-03-00. Pubmed ID: 36724552; DOI: 10.1016/j.scr.2023.103036 UGENTi001-AUGENTi001-A-1 2023-03-00 2023-03-00 PubMed: 36724552 DOI: 10.1016/j.scr.2023.103036Associated cell lines:
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Kamat K, Inamdar MS
Generation of OCIAD2 homozygous knockout (BJNhem20-OCIAD2-CRISPR-33) and heterozygous knockout (BJNhem20-OCIAD2-CRISPR-40) human embryonic stem cell lines using CRISPR-Cas9 mediated targeting
Kamat K et al. Generation of OCIAD2 homozygous knockout (BJNhem20-OCIAD2-CRISPR-33) and heterozygous knockout (BJNhem20-OCIAD2-CRISPR-40) human embryonic stem cell lines using CRISPR-Cas9 mediated targeting. . 2023-03-00. Pubmed ID: 36642056; DOI: 10.1016/j.scr.2023.103026 JNCSRe002-A-1JNCSRe002-A-2 2023-03-00 2023-03-00 PubMed: 36642056 DOI: 10.1016/j.scr.2023.103026Associated cell lines:
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Ceschin II, Ceschin AP, Joya MS, Mitsugi TG, Nishikawa LK, Krepischi AC, Okamoto OK
Functional assessment of donated human embryos for the generation of pluripotent embryonic stem cell lines
Ceschin II et al. Functional assessment of donated human embryos for the generation of pluripotent embryonic stem cell lines. . 2023-03-00. Pubmed ID: 36737274; DOI: 10.1016/j.rbmo.2022.11.020 FDCHi004-A 2023-03-00 2023-03-00 PubMed: 36737274 DOI: 10.1016/j.rbmo.2022.11.020Associated cell lines:
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Bai J, Zhang J, Fu W, Li S, Tian X, Li X, Zhao X, Dong J
Generation of a TRPM8 knockout hESC line (WAe009-A-A) derived from H9 using CRISPR/Cas9
Bai J et al. Generation of a TRPM8 knockout hESC line (WAe009-A-A) derived from H9 using CRISPR/Cas9. . 2023-03-00. Pubmed ID: 36796252; DOI: 10.1016/j.scr.2023.103040 WAe009-AWAe009-A-A 2023-03-00 2023-03-00 PubMed: 36796252 DOI: 10.1016/j.scr.2023.103040Associated cell lines:
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Prakash A, Kamat K, Inamdar MS
Generation of an OCIAD2 overexpressing transgenic human embryonic stem cell line, BJNhem20-OCIAD2-OV
Prakash A et al. Generation of an OCIAD2 overexpressing transgenic human embryonic stem cell line, BJNhem20-OCIAD2-OV. . 2023-03-00. Pubmed ID: 36640474; DOI: 10.1016/j.scr.2023.103027 JNCSRe002-A-3 2023-03-00 2023-03-00 PubMed: 36640474 DOI: 10.1016/j.scr.2023.103027Associated cell lines:
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Guo R, Yuan S, Li B, Wang J, Sun C
Generation of NANOS3-mCherry reporter human embryonic stem cell line SYSUe-009-A using CRISPR/Cas9
Guo R et al. Generation of NANOS3-mCherry reporter human embryonic stem cell line SYSUe-009-A using CRISPR/Cas9. . 2023-03-00. Pubmed ID: 36630838; DOI: 10.1016/j.scr.2023.103022 SYSUe009-A 2023-03-00 2023-03-00 PubMed: 36630838 DOI: 10.1016/j.scr.2023.103022Associated cell lines:
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Yi T, Liu J, Zhang S, He Y, Han J
Generation of a TIMP3 knockout stem cell line via CRISPR/Cas9 system
Yi T et al. Generation of a TIMP3 knockout stem cell line via CRISPR/Cas9 system. . 2023-03-00. Pubmed ID: 36716678; DOI: 10.1016/j.scr.2023.103034 WAe009-AZZUNEUi008-AWAe009-A-89 2023-03-00 2023-03-00 PubMed: 36716678 DOI: 10.1016/j.scr.2023.103034Associated cell lines:
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Rabino M, Rurali E, Zamboni C, Rovina D, Mallia S, Cauteruccio M, Baggiano A, Giacari CM, Bellin M, Pompilio G
Generation of four human induced pluripotent stem cell lines from COVID-19 hospitalized patients with increased levels of cardiac Troponin in the acute infection phase developing or not myocarditis
Rabino M et al. Generation of four human induced pluripotent stem cell lines from COVID-19 hospitalized patients with increased levels of cardiac Troponin in the acute infection phase developing or not myocarditis. . 2023-03-00. Pubmed ID: 36630840; DOI: 10.1016/j.scr.2023.103018; PMC: PMC9812822 CCMi005-ACCMi007-ACCMi008-ACCMi009-ACCMi011-A 2023-03-00 2023-03-00 PubMed: 36630840 DOI: 10.1016/j.scr.2023.103018 -
Haag C, Uysal B, Marquetand J, Löffler H, Mau-Holzmann UA, Lerche H, Schwarz N
Generation of an induced pluripotent stem cell (iPSC) line from a patient with GEFS+ carrying a STX1B (p.Lys45delinsArgMetCysIleGlu and p.Leu46Met) mutation
Haag C et al. Generation of an induced pluripotent stem cell (iPSC) line from a patient with GEFS+ carrying a STX1B (p.Lys45delinsArgMetCysIleGlu and p.Leu46Met) mutation. . 2023-03-00. Pubmed ID: 36652844; DOI: 10.1016/j.scr.2023.103028 HIHDNEi004-A 2023-03-00 2023-03-00 PubMed: 36652844 DOI: 10.1016/j.scr.2023.103028Associated cell lines:
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McNeill RV, Radtke F, Nieberler M, Koreny C, Chiocchetti AG, Kittel-Schneider S
Generation of four human induced pluripotent stem cells derived from ADHD patients carrying different genotypes for the risk SNP rs1397547 in the ADHD-associated gene ADGRL3
McNeill RV et al. Generation of four human induced pluripotent stem cells derived from ADHD patients carrying different genotypes for the risk SNP rs1397547 in the ADHD-associated gene ADGRL3. . 2023-03-00. Pubmed ID: 36640473; DOI: 10.1016/j.scr.2023.103016 UKWi002-AUKWi002-A-1UKWi003-AUKWi003-A-1UKWi004-AUKWi004-A-1UKWi005-AUKWi005-A-1 2023-03-00 2023-03-00 PubMed: 36640473 DOI: 10.1016/j.scr.2023.103016Associated cell lines:
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Van Den Heuvel LJF, Peeters S, Meester JAN, Perik M, Coucke P, Loeys BL
A generated induced pluripotent stem cell (iPSC) line (CMGANTi005-A) of a Marfan syndrome patient with an FBN1 c.7754T > C (p.Ile2585Thr) variation
Van Den Heuvel LJF et al. A generated induced pluripotent stem cell (iPSC) line (CMGANTi005-A) of a Marfan syndrome patient with an FBN1 c.7754T > C (p.Ile2585Thr) variation. . 2023-03-00. Pubmed ID: 36708686; DOI: 10.1016/j.scr.2023.103032 BBANTWi006-ABBANTWi007-ACMGANTi005-A 2023-03-00 2023-03-00 PubMed: 36708686 DOI: 10.1016/j.scr.2023.103032Associated cell lines:
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Xu Zhi-Xiang, Zhou Yi-Yan, Wu Rong, Zhao Ya-Jie, Wang Xiao-Ping
Brain iron deposition and whole-exome sequencing of non-Wilson's disease hypoceruloplasminemia in a family
Xu Zhi-Xiang et al. Brain iron deposition and whole-exome sequencing of non-Wilson's disease hypoceruloplasminemia in a family. . 2023-03-00. DOI: 10.1016/j.jnrt.2022.100027 THSJTUi001-A 2023-03-00 2023-03-00 DOI: 10.1016/j.jnrt.2022.100027Associated cell lines:
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Iannello Grazia, Patel Achchhe, Sirabella Dario, Diaz Alejandro Garcia, Hoover Benjamin N., Sarmah Hemanta, Corneo Barbara
Simple, Fast, and Efficient Method for Derivation of Dermal Fibroblasts From Skin Biopsies
Iannello Grazia et al. Simple, Fast, and Efficient Method for Derivation of Dermal Fibroblasts From Skin Biopsies. . 2023-03-00. DOI: 10.1002/cpz1.714 SEIi001-AFRIMOi001-A 2023-03-00 2023-03-00 DOI: 10.1002/cpz1.714Associated cell lines:
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Zushin PH, Zhou Y, Li A, Ashley EA, Wheeler MT, Wu JC
Generation of two human iPSC lines with Exon 3 mutations in BCL2-Associated Athanogene 3 (BAG3) from dilated cardiomyopathy patients
Zushin PH et al. Generation of two human iPSC lines with Exon 3 mutations in BCL2-Associated Athanogene 3 (BAG3) from dilated cardiomyopathy patients. . 2023-03-00. Pubmed ID: 36642055; DOI: 10.1016/j.scr.2023.103019; PMC: PMC10042224 SCVIi073-ASCVIi074-A 2023-03-00 2023-03-00 PubMed: 36642055 DOI: 10.1016/j.scr.2023.103019Associated cell lines:
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Klug K, Breyer M, Klopocki E, Üçeyler N
Generation of two induced pluripotent stem cell lines UKWNLi006 and UKWNLi007 derived from two patients with an active site GLA mutation leading to a pain and no pain phenotype in Fabry disease
Klug K et al. Generation of two induced pluripotent stem cell lines UKWNLi006 and UKWNLi007 derived from two patients with an active site GLA mutation leading to a pain and no pain phenotype in Fabry disease. . 2023-03-00. Pubmed ID: 36640471; DOI: 10.1016/j.scr.2023.103025 UKWNLi006-AUKWNLi007-AUKWNLi006-BUKWNLi007-B 2023-03-00 2023-03-00 PubMed: 36640471 DOI: 10.1016/j.scr.2023.103025Associated cell lines:
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He Z, Sun H, Yu T, Yang Y, Zhang X, Yang Y
Generation of a human embryonic stem cell line (SKLRMe004-A) carrying NKX2.5-EGFP and TBX5-Tdtomato dual fluorescent reporters
He Z et al. Generation of a human embryonic stem cell line (SKLRMe004-A) carrying NKX2.5-EGFP and TBX5-Tdtomato dual fluorescent reporters. . 2023-03-00. Pubmed ID: 36608451; DOI: 10.1016/j.scr.2023.103015 WAe009-A-H 2023-03-00 2023-03-00 PubMed: 36608451 DOI: 10.1016/j.scr.2023.103015Associated cell lines:
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De Kinderen P, Peeters S, Rabaut L, Mortier G, Ponsaerts P, Loeys B, Verstraeten A, Meester JAN
IPSC reprogramming of two patients with spondyloepimetaphyseal dysplasia (SEMD, biglycan type)
De Kinderen P et al. IPSC reprogramming of two patients with spondyloepimetaphyseal dysplasia (SEMD, biglycan type). . 2023-03-00. Pubmed ID: 36640472; DOI: 10.1016/j.scr.2023.103024; PMC: PMC9972783 CMGANTi003-ACMGANTi004-A 2023-03-00 2023-03-00 PubMed: 36640472 DOI: 10.1016/j.scr.2023.103024Associated cell lines:
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Jauvin D, Pierre M, Boutjdir M, Puymirat J, Chahine M
Generation of four myotonic dystrophy type 1 patient iPSC lines (CBRCULi002-A, CBRCULi003-A, CBRCULi004-A, CBRCULi005-A) and a control (CBRCULi001-A) derived from lymphoblastoids cell lines
Jauvin D et al. Generation of four myotonic dystrophy type 1 patient iPSC lines (CBRCULi002-A, CBRCULi003-A, CBRCULi004-A, CBRCULi005-A) and a control (CBRCULi001-A) derived from lymphoblastoids cell lines. . 2023-03-00. Pubmed ID: 36739767; DOI: 10.1016/j.scr.2023.103037 CHUQi001-ACBRCULi001-ACBRCULi002-ACBRCULi003-ACBRCULi004-ACBRCULi005-A 2023-03-00 2023-03-00 PubMed: 36739767 DOI: 10.1016/j.scr.2023.103037Associated cell lines:
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Rotundo G, Turco EM, Ruotolo G, Torrente I, Candido O, Lopez G, Ferrari D, Caputi C, Mastrangelo M, Pisani F, Gelati M, Guarnieri V, Vescovi AL, Rosati J
Generation of an induced pluripotent stem cell line CSSi015-A (9553), carrying a point mutation c.2915C > T in the human calcium sensing receptor (CasR) gene
Rotundo G et al. Generation of an induced pluripotent stem cell line CSSi015-A (9553), carrying a point mutation c.2915C > T in the human calcium sensing receptor (CasR) gene. . 2023-03-00. Pubmed ID: 36638628; DOI: 10.1016/j.scr.2023.103023 CSSi014-ACSSi015-A 2023-03-00 2023-03-00 PubMed: 36638628 DOI: 10.1016/j.scr.2023.103023 -
Nehra S, Sharma V, Umrani M, Singhal N
Generation of integration-free Down syndrome and isogenic euploid human induced pluripotent stem cells
Nehra S et al. Generation of integration-free Down syndrome and isogenic euploid human induced pluripotent stem cells. . 2023-03-00. Pubmed ID: 36764067; DOI: 10.1016/j.scr.2023.103041 NSi001-ANSi001-BNSi001-CNSi003-ANSi003-B 2023-03-00 2023-03-00 PubMed: 36764067 DOI: 10.1016/j.scr.2023.103041 -
Srisook P, Laowtammathron C, Lorthongpanich C, Klaihmon P, Terbto P, Waeteekul S, U-Pratya Y, Issaragrisil S
Generation of RUNX1c-eGFP induced pluripotent stem cell, MUSIi012-A-4, using CRISPR/Cas9
Srisook P et al. Generation of RUNX1c-eGFP induced pluripotent stem cell, MUSIi012-A-4, using CRISPR/Cas9. . 2023-03-00. Pubmed ID: 36753833; DOI: 10.1016/j.scr.2023.103035 MUSIi012-AMUSIi012-A-4 2023-03-00 2023-03-00 PubMed: 36753833 DOI: 10.1016/j.scr.2023.103035Associated cell lines:
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Cheng S, Liu X, Yuan L, Wang N, Zhang ZC, Han J
The role of PQBP1 in neural development and function
Cheng S et al. The role of PQBP1 in neural development and function. . 2023-02-27. Pubmed ID: 36815699; DOI: 10.1042/bst20220920 WMUi017-A 2023-02-27 2023-02-27 PubMed: 36815699 DOI: 10.1042/bst20220920Associated cell lines:
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Kim NG, Jung DJ, Jung YK, Kang KS
The Effect of a Novel Mica Nanoparticle, STB-MP, on an Alzheimer's Disease Patient-Induced PSC-Derived Cortical Brain Organoid Model
Kim NG et al. The Effect of a Novel Mica Nanoparticle, STB-MP, on an Alzheimer's Disease Patient-Induced PSC-Derived Cortical Brain Organoid Model. . 2023-02-27. Pubmed ID: 36903771; DOI: 10.3390/nano13050893; PMC: PMC10005775 KSCBi005-A 2023-02-27 2023-02-27 PubMed: 36903771 DOI: 10.3390/nano13050893Associated cell lines:
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Nazarenko Maria S., Sleptcov Aleksei A., Zarubin Aleksei A., Salakhov Ramil R., Shevchenko Alexander I., Tmoyan Narek A., Elisaphenko Eugeny A., Zubkova Ekaterina S., Zheltysheva Nina V., Ezhov Marat V., Kukharchuk Valery V., Parfyonova Yelena V., Zakian Suren M., Zakharova Irina S.
Calling and Phasing of Single-Nucleotide and Structural Variants of the LDLR Gene Using Oxford Nanopore MinION
Nazarenko Maria S. et al. Calling and Phasing of Single-Nucleotide and Structural Variants of the LDLR Gene Using Oxford Nanopore MinION. . 2023-02-24. DOI: 10.3390/ijms24054471 ICGi036-AICGi037-AICGi038-A 2023-02-24 2023-02-24 DOI: 10.3390/ijms24054471 -
Grigor'eva EV, Kopytova AE, Yarkova ES, Pavlova SV, Sorogina DA, Malakhova AA, Malankhanova TB, Baydakova GV, Zakharova EY, Medvedev SP, Pchelina SN, Zakian SM
Biochemical Characteristics of iPSC-Derived Dopaminergic Neurons from N370S GBA Variant Carriers with and without Parkinson's Disease
Grigor'eva EV et al. Biochemical Characteristics of iPSC-Derived Dopaminergic Neurons from N370S GBA Variant Carriers with and without Parkinson's Disease. . 2023-02-23. Pubmed ID: 36901867; DOI: 10.3390/ijms24054437; PMC: PMC10002967 ICGi021-AICGi022-AICGi034-AICGi034-BICGi034-CICGi039-AICGi039-BICGi039-C 2023-02-23 2023-02-23 PubMed: 36901867 DOI: 10.3390/ijms24054437 -
Cichocki F, van der Stegen SJC, Miller JS
Engineered and banked iPSCs for advanced NK- and T-cell immunotherapies
Cichocki F et al. Engineered and banked iPSCs for advanced NK- and T-cell immunotherapies. . 2023-02-23. Pubmed ID: 36327161; DOI: 10.1182/blood.2022016205; PMC: PMC10023718 MUSIi013-A 2023-02-23 2023-02-23 PubMed: 36327161 DOI: 10.1182/blood.2022016205Associated cell lines:
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Cui S, Fang X, Lee H, Shin YJ, Koh ES, Chung S, Park HS, Lim SW, Lee KI, Lee JY, Yang CW, Chung BH
Modeling of Fabry disease nephropathy using patient derived human induced pluripotent stem cells and kidney organoid system
Cui S et al. Modeling of Fabry disease nephropathy using patient derived human induced pluripotent stem cells and kidney organoid system. . 2023-02-22. Pubmed ID: 36814269; DOI: 10.1186/s12967-023-03992-0; PMC: PMC9948377 CMCi002-AMUi027-ACMCi006-ACMCi007-A 2023-02-22 2023-02-22 PubMed: 36814269 DOI: 10.1186/s12967-023-03992-0 -
Liao Xufeng, Wang Yingxing, Lai Xinsheng, Wang Shunqi
The role of Rapsyn in neuromuscular junction and congenital myasthenic syndrome
Liao Xufeng et al. The role of Rapsyn in neuromuscular junction and congenital myasthenic syndrome. . 2023-02-20. DOI: 10.17305/bb.2022.8641 SDQLCHi018-A 2023-02-20 2023-02-20 DOI: 10.17305/bb.2022.8641Associated cell lines:
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Mollashahi B, Latifi-Navid H, Owliaee I, Shamdani S, Uzan G, Jamehdor S, Naserian S
Research and Therapeutic Approaches in Stem Cell Genome Editing by CRISPR Toolkit
Mollashahi B et al. Research and Therapeutic Approaches in Stem Cell Genome Editing by CRISPR Toolkit. . 2023-02-20. Pubmed ID: 36838970; DOI: 10.3390/molecules28041982; PMC: PMC9961668 KSCBi005-AKSCBi005-A-1KSCBi005-A-3MUSIi012-AMUSIi012-A-1UMi028-AUMi028-A-2 2023-02-20 2023-02-20 PubMed: 36838970 DOI: 10.3390/molecules28041982Associated cell lines:
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Becerra-Calixto A, Mukherjee A, Ramirez S, Sepulveda S, Sinha T, Al-Lahham R, De Gregorio N, Gherardelli C, Soto C
Lewy Body-like Pathology and Loss of Dopaminergic Neurons in Midbrain Organoids Derived from Familial Parkinson's Disease Patient
Becerra-Calixto A et al. Lewy Body-like Pathology and Loss of Dopaminergic Neurons in Midbrain Organoids Derived from Familial Parkinson's Disease Patient. . 2023-02-15. Pubmed ID: 36831291; DOI: 10.3390/cells12040625; PMC: PMC9954141 EDi044-A 2023-02-15 2023-02-15 PubMed: 36831291 DOI: 10.3390/cells12040625Associated cell lines:
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Yin XY, Chen HX, Chen Z, Yang Q, Han J, He GW
Genetic Variants of ISL1 Gene Promoter Identified from Congenital Tetralogy of Fallot Patients Alter Cellular Function Forming Disease Basis
Yin XY et al. Genetic Variants of ISL1 Gene Promoter Identified from Congenital Tetralogy of Fallot Patients Alter Cellular Function Forming Disease Basis. . 2023-02-13. Pubmed ID: 36830727; DOI: 10.3390/biom13020358; PMC: PMC9953631 YAHKMUi001-A 2023-02-13 2023-02-13 PubMed: 36830727 DOI: 10.3390/biom13020358Associated cell lines:
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Siles L, Gaudó P, Pomares E
High-Efficiency CRISPR/Cas9-Mediated Correction of a Homozygous Mutation in Achromatopsia-Patient-Derived iPSCs
Siles L et al. High-Efficiency CRISPR/Cas9-Mediated Correction of a Homozygous Mutation in Achromatopsia-Patient-Derived iPSCs. . 2023-02-11. Pubmed ID: 36835061; DOI: 10.3390/ijms24043655; PMC: PMC9964936 FRIMOi007-A 2023-02-11 2023-02-11 PubMed: 36835061 DOI: 10.3390/ijms24043655Associated cell lines:
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Bérenger-Currias N, Martinat C, Baghdoyan S
Pluripotent Stem Cells in Disease Modeling and Drug Discovery for Myotonic Dystrophy Type 1
Bérenger-Currias N et al. Pluripotent Stem Cells in Disease Modeling and Drug Discovery for Myotonic Dystrophy Type 1. . 2023-02-10. Pubmed ID: 36831237; DOI: 10.3390/cells12040571; PMC: PMC9954118 CHUQi001-AZZUi006-A 2023-02-10 2023-02-10 PubMed: 36831237 DOI: 10.3390/cells12040571Associated cell lines:
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Park Sangbae, Gwon Yonghyun, Khan Shahidul Ahmed, Jang Kyoung-Je, Kim Jangho
Engineering considerations of iPSC-based personalized medicine
Park Sangbae et al. Engineering considerations of iPSC-based personalized medicine. . 2023-02-09. DOI: 10.1186/s40824-023-00382-x HIHDNEi002-AMCRIi001-AMCRIi001-A-1 2023-02-09 2023-02-09 DOI: 10.1186/s40824-023-00382-xAssociated cell lines:
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Inácio JM, Nunes MM, Almeida M, Cristo F, Anjos R, Belo JA
Gene-Edited Human-Induced Pluripotent Stem Cell Lines to Elucidate DAND5 Function throughout Cardiac Differentiation
Inácio JM et al. Gene-Edited Human-Induced Pluripotent Stem Cell Lines to Elucidate DAND5 Function throughout Cardiac Differentiation. . 2023-02-05. Pubmed ID: 36831187; DOI: 10.3390/cells12040520; PMC: PMC9954670 NMSUNLi001-A 2023-02-05 2023-02-05 PubMed: 36831187 DOI: 10.3390/cells12040520Associated cell lines:
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Lim SW, Fang X, Cui S, Lee H, Shin YJ, Ko EJ, Lee KI, Lee JY, Chung BH, Yang CW
CRISPR-Cas9-Mediated Correction of SLC12A3 Gene Mutation Rescues the Gitelman's Disease Phenotype in a Patient-Derived Kidney Organoid System
Lim SW et al. CRISPR-Cas9-Mediated Correction of SLC12A3 Gene Mutation Rescues the Gitelman's Disease Phenotype in a Patient-Derived Kidney Organoid System. . 2023-02-03. Pubmed ID: 36769335; DOI: 10.3390/ijms24033019; PMC: PMC9917614 CMCi002-A 2023-02-03 2023-02-03 PubMed: 36769335 DOI: 10.3390/ijms24033019Associated cell lines:
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Kleynerman A, Rybova J, Faber ML, McKillop WM, Levade T, Medin JA
Acid Ceramidase Deficiency: Bridging Gaps between Clinical Presentation, Mouse Models, and Future Therapeutic Interventions
Kleynerman A et al. Acid Ceramidase Deficiency: Bridging Gaps between Clinical Presentation, Mouse Models, and Future Therapeutic Interventions. . 2023-02-01. Pubmed ID: 36830643; DOI: 10.3390/biom13020274; PMC: PMC9953133 TRNDi030-A 2023-02-01 2023-02-01 PubMed: 36830643 DOI: 10.3390/biom13020274Associated cell lines:
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Joachimiak P, Ciesiołka A, Kozłowska E, Świtoński PM, Figura G, Ciołak A, Adamek G, Surdyka M, Kalinowska-Pośka Ż, Figiel M, Caron NS, Hayden MR, Fiszer A
Allele-specific quantitation of ATXN3 and HTT transcripts in polyQ disease models
Joachimiak P et al. Allele-specific quantitation of ATXN3 and HTT transcripts in polyQ disease models. . 2023-02-01. Pubmed ID: 36726088; DOI: 10.1186/s12915-023-01515-3; PMC: PMC9893648 IBCHi002-A 2023-02-01 2023-02-01 PubMed: 36726088 DOI: 10.1186/s12915-023-01515-3Associated cell lines:
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Jimenez-Tellez N, Vera CD, Yildirim Z, Vicente Guevara J, Zhang T, Wu JC
Generation of two iPSC lines from long QT syndrome patients carrying SNTA1 variants
Jimenez-Tellez N et al. Generation of two iPSC lines from long QT syndrome patients carrying SNTA1 variants. . 2023-02-00. Pubmed ID: 36528013; DOI: 10.1016/j.scr.2022.103003; PMC: PMC10029814 WAe009-AWAe009-A-50SCVIi061-ASCVIi062-A 2023-02-00 2023-02-00 PubMed: 36528013 DOI: 10.1016/j.scr.2022.103003Associated cell lines:
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Adhicary S, Ye S, Lin H, Texter K, Garg V, Zhao MT
Establishment of NCHi009-A, an iPSC line from a patient with hypoplastic left heart syndrome (HLHS) carrying a heterozygous NOTCH1 mutation
Adhicary S et al. Establishment of NCHi009-A, an iPSC line from a patient with hypoplastic left heart syndrome (HLHS) carrying a heterozygous NOTCH1 mutation. . 2023-02-00. Pubmed ID: 36599283; DOI: 10.1016/j.scr.2022.103013; PMC: PMC9904404 NCHi009-A 2023-02-00 2023-02-00 PubMed: 36599283 DOI: 10.1016/j.scr.2022.103013Associated cell lines:
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Sugie K
Editorial commentary: Highlighting the ray of hope in Danon disease research after 40 years
Sugie K. Editorial commentary: Highlighting the ray of hope in Danon disease research after 40 years. . 2023-02-00. Pubmed ID: 34863946; DOI: 10.1016/j.tcm.2021.11.007 ZZUNEUi020-A 2023-02-00 2023-02-00 PubMed: 34863946 DOI: 10.1016/j.tcm.2021.11.007Associated cell lines:
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Zhou M, Ni J, Huang P, Liu X
Generation of a doxycycline-inducible ETV2 expression cell line using PiggyBac transposase system
Zhou M et al. Generation of a doxycycline-inducible ETV2 expression cell line using PiggyBac transposase system. . 2023-02-00. Pubmed ID: 36463633; DOI: 10.1016/j.scr.2022.102985 WAe009-A-92 2023-02-00 2023-02-00 PubMed: 36463633 DOI: 10.1016/j.scr.2022.102985Associated cell lines:
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Lahm H, Stieglbauer S, Neb I, Doppler SA, Schneider S, Dzilic E, Lange R, Krane M, Dreßen M
Generation of two CRISPR/Cas edited human induced pluripotent stem cell lines (DHMi005-A-3 and DHMi005-A-4) carrying a FLAG-tag after exon 9 of the TBX5 gene
Lahm H et al. Generation of two CRISPR/Cas edited human induced pluripotent stem cell lines (DHMi005-A-3 and DHMi005-A-4) carrying a FLAG-tag after exon 9 of the TBX5 gene. . 2023-02-00. Pubmed ID: 36610218; DOI: 10.1016/j.scr.2022.103011 DHMi005-ADHMi005-A-3DHMi005-A-4 2023-02-00 2023-02-00 PubMed: 36610218 DOI: 10.1016/j.scr.2022.103011Associated cell lines:
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Grigor’eva E. V., Pavlova S. V., Malakhova A. A., Yarkova E. S., Sorogina D. A., Minina J. M., Miliukhina I. V., Nikolaev M. A., Pchelina S. N., Medvedev S. P., Zakian S. M.
Generation of an Induced Pluripotent Stem Cell Line, ICGi043-A, by Reprogramming Peripheral Blood Mononuclear Cells from a Parkinson’s Disease Patient with p.G2019S Mutation in the LRRK2 Gene
Grigor’eva E. V. et al. Generation of an Induced Pluripotent Stem Cell Line, ICGi043-A, by Reprogramming Peripheral Blood Mononuclear Cells from a Parkinson’s Disease Patient with p.G2019S Mutation in the LRRK2 Gene. . 2023-02-00. DOI: 10.1134/s1062360423010058 ICGi043-A 2023-02-00 2023-02-00 DOI: 10.1134/s1062360423010058Associated cell lines:
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Dhuriya YK, Naik AA
CRISPR: a tool with potential for genomic reprogramming in neurological disorders
Dhuriya YK et al. CRISPR: a tool with potential for genomic reprogramming in neurological disorders. . 2023-02-00. Pubmed ID: 36507966; DOI: 10.1007/s11033-022-08136-z WAe009-AWAe009-A-16 2023-02-00 2023-02-00 PubMed: 36507966 DOI: 10.1007/s11033-022-08136-zAssociated cell lines:
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Sun J, Lu P, Shen Y, Ma L
Generation of an induced pluripotent stem cell line (SHCDNi007-A) from a patient with pyruvate carboxylase deficiency carrying compound heterozygous (c.182 T > C/ c.2581G > A) variants in PC
Sun J et al. Generation of an induced pluripotent stem cell line (SHCDNi007-A) from a patient with pyruvate carboxylase deficiency carrying compound heterozygous (c.182 T > C/ c.2581G > A) variants in PC. . 2023-02-00. Pubmed ID: 36508859; DOI: 10.1016/j.scr.2022.102997 SHCDNi007-A 2023-02-00 2023-02-00 PubMed: 36508859 DOI: 10.1016/j.scr.2022.102997Associated cell lines:
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Konala VBR, Nandakumar S, Battu R, Pal R
Corrigendum to "Derivation of three induced pluripotent stem cell lines under feeder-free culture conditions from peripheral blood mononuclear cells (PBMC) of Indian patients suffering from inherited retinal diseases carrying different mutations" [Stem Cell Res. 45 (2020) 101757]
Konala VBR et al. Corrigendum to "Derivation of three induced pluripotent stem cell lines under feeder-free culture conditions from peripheral blood mononuclear cells (PBMC) of Indian patients suffering from inherited retinal diseases carrying different mutations" [Stem Cell Res. 45 (2020) 101757]. . 2023-02-00. Pubmed ID: 36528015; DOI: 10.1016/j.scr.2022.103005 ERPLi001-AERPLi002-AERPLi003-A 2023-02-00 2023-02-00 PubMed: 36528015 DOI: 10.1016/j.scr.2022.103005Associated cell lines:
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Choi JB, Seo D, Do HS, Han YM
Generation of a CRISPR/Cas9-corrected-hiPSC line (DDLABi001-A) from Fabry disease (FD)-derived iPSCs having α-galactosidase (GLA) gene mutation (c.803_806del)
Choi JB et al. Generation of a CRISPR/Cas9-corrected-hiPSC line (DDLABi001-A) from Fabry disease (FD)-derived iPSCs having α-galactosidase (GLA) gene mutation (c.803_806del). . 2023-02-00. Pubmed ID: 36516658; DOI: 10.1016/j.scr.2022.103001 DDLABi001-A 2023-02-00 2023-02-00 PubMed: 36516658 DOI: 10.1016/j.scr.2022.103001Associated cell lines:
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Wang J, Long P, Tian S, Zu W, Liu J, Wu B, Mao J, Li D, Ma Y, Huang Y
Cyclosporin A Promotes Invasion and Migration of Extravillous Trophoblast Cells Derived from Human-Induced Pluripotent Stem Cells and Human Embryonic Stem Cells
Wang J et al. Cyclosporin A Promotes Invasion and Migration of Extravillous Trophoblast Cells Derived from Human-Induced Pluripotent Stem Cells and Human Embryonic Stem Cells. . 2023-02-00. Pubmed ID: 36476041; DOI: 10.1089/scd.2022.0144 HNMUi002-AHNMUi003-AHNMUi004-AHNMUi005-AHNMUi006-AHNMUi007-AHNMUi008-AHNMUi009-AHNMUi010-A 2023-02-00 2023-02-00 PubMed: 36476041 DOI: 10.1089/scd.2022.0144Associated cell lines:
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Jin Y, Nan G
Generation of induced pluripotent stem cell(iPSC)line CJUHi001-A derived peripheral blood mononuclear cells of spinocerebellar ataxia type 1(SCA1) the CAG repeat mutation in ATXN1 gene
Jin Y et al. Generation of induced pluripotent stem cell(iPSC)line CJUHi001-A derived peripheral blood mononuclear cells of spinocerebellar ataxia type 1(SCA1) the CAG repeat mutation in ATXN1 gene. . 2023-02-00. Pubmed ID: 36459834; DOI: 10.1016/j.scr.2022.102975 CJUHi001-A 2023-02-00 2023-02-00 PubMed: 36459834 DOI: 10.1016/j.scr.2022.102975Associated cell lines:
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Kang EH, Kim JW, Noh H, Park SH, Park HJ, Yoon S, Kim H
Establishment of a human embryonic stem cell line, WAe009-A-99, with constitutive expression of the dCas9-p300 fusion protein
Kang EH et al. Establishment of a human embryonic stem cell line, WAe009-A-99, with constitutive expression of the dCas9-p300 fusion protein. . 2023-02-00. Pubmed ID: 36493708; DOI: 10.1016/j.scr.2022.102986 WAe009-AWAe009-A-99 2023-02-00 2023-02-00 PubMed: 36493708 DOI: 10.1016/j.scr.2022.102986Associated cell lines:
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Keller AL, Greis D, Eybe J, Plöger S, Weiss M, Koch A, Brucker SY, Schenke-Layland K, Schmees C
Generation and characterization of three induced pluripotent stem cells lines from an 86-year old female individual diagnosed with an invasive lobular mammary carcinoma
Keller AL et al. Generation and characterization of three induced pluripotent stem cells lines from an 86-year old female individual diagnosed with an invasive lobular mammary carcinoma. . 2023-02-00. Pubmed ID: 36528016; DOI: 10.1016/j.scr.2022.102988 NMIi012-BNMIi012-DNMIi012-E 2023-02-00 2023-02-00 PubMed: 36528016 DOI: 10.1016/j.scr.2022.102988 -
Santangelo S, Bossolasco P, Magri S, Colombrita C, Invernizzi S, Gellera C, Nanetti L, Di Bella D, Silani V, Taroni F, Ratti A
Generation of an iPSC line from a patient with spastic paraplegia type 10 carrying a novel mutation in KIF5A gene
Santangelo S et al. Generation of an iPSC line from a patient with spastic paraplegia type 10 carrying a novel mutation in KIF5A gene. . 2023-02-00. Pubmed ID: 36565680; DOI: 10.1016/j.scr.2022.103008 IAIi010-A 2023-02-00 2023-02-00 PubMed: 36565680 DOI: 10.1016/j.scr.2022.103008Associated cell lines:
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Blanch-Asensio A, van der Vaart B, Vinagre M, Groen E, Arendzen C, Freund C, Geijsen N, Mummery CL, Davis RP
Generation of AAVS1 and CLYBL STRAIGHT-IN v2 acceptor human iPSC lines for integrating DNA payloads
Blanch-Asensio A et al. Generation of AAVS1 and CLYBL STRAIGHT-IN v2 acceptor human iPSC lines for integrating DNA payloads. . 2023-02-00. Pubmed ID: 36495703; DOI: 10.1016/j.scr.2022.102991 LUMCi004-ALUMCi004-A-1LUMCi004-A-2 2023-02-00 2023-02-00 PubMed: 36495703 DOI: 10.1016/j.scr.2022.102991Associated cell lines:
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Conteduca G, Baldo C, Arado A, Traverso M, Testa B, Malacarne M, Coviello D, Zara F, Baldassari S
Generation of induced pluripotent stem cell lines from a patient with Sotos syndrome carrying 5q35 microdeletion
Conteduca G et al. Generation of induced pluripotent stem cell lines from a patient with Sotos syndrome carrying 5q35 microdeletion. . 2023-02-00. Pubmed ID: 36580887; DOI: 10.1016/j.scr.2022.103007 IGGi001-AIGGi001-B 2023-02-00 2023-02-00 PubMed: 36580887 DOI: 10.1016/j.scr.2022.103007 -
Polak K, Stępniewski J, Ścieżyńska A, Podgórska A, Dulak J, Florczyk-Soluch U
Generation of human induced pluripotent stem cell lines with HMOX1 promoter polymorphism and CRISPR/Cas9-mediated deletion of exon 50 of DMD gene
Polak K et al. Generation of human induced pluripotent stem cell lines with HMOX1 promoter polymorphism and CRISPR/Cas9-mediated deletion of exon 50 of DMD gene. . 2023-02-00. Pubmed ID: 36565681; DOI: 10.1016/j.scr.2022.103004 DMBi005-ADMBi005-A-1DMBi006-ADMBi006-A-1 2023-02-00 2023-02-00 PubMed: 36565681 DOI: 10.1016/j.scr.2022.103004Associated cell lines:
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Yang X, Liu C, Zhang H, Lv Y, Li Y, Li Z, Liu Y, Gai Z
Establishment of an induced pluripotent stem cell (iPSC) line SDQLCHi045-A from peripheral blood mononuclear cells of a patient with Coffin-Siris syndrome 1 carrying a mutation in ARID1B gene
Yang X et al. Establishment of an induced pluripotent stem cell (iPSC) line SDQLCHi045-A from peripheral blood mononuclear cells of a patient with Coffin-Siris syndrome 1 carrying a mutation in ARID1B gene. . 2023-02-00. Pubmed ID: 36473251; DOI: 10.1016/j.scr.2022.102982 SDQLCHi045-A 2023-02-00 2023-02-00 PubMed: 36473251 DOI: 10.1016/j.scr.2022.102982Associated cell lines:
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Li Z, Liu C, Xin H, Yang Y, Wang Y, Niu S, Gao C, Gai Z, Liu Y
Establishment of a transgene-free iPS cell line (SDQLCHi046-A) from a young patient bearing a HDAC8 mutation and suffering from Cornelia de Lange Syndrome
Li Z et al. Establishment of a transgene-free iPS cell line (SDQLCHi046-A) from a young patient bearing a HDAC8 mutation and suffering from Cornelia de Lange Syndrome. . 2023-02-00. Pubmed ID: 36481505; DOI: 10.1016/j.scr.2022.102984 SDQLCHi046-A 2023-02-00 2023-02-00 PubMed: 36481505 DOI: 10.1016/j.scr.2022.102984Associated cell lines:
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Koemans EA, Castello JP, Rasing I, Abramson JR, Voigt S, Perosa V, van Harten TW, van Zwet EW, Terwindt GM, Gurol ME, Rosand J, Greenberg SM, van Walderveen MAA, Biffi A, Viswanathan A, Wermer MJH
Sex Differences in Onset and Progression of Cerebral Amyloid Angiopathy
Koemans EA et al. Sex Differences in Onset and Progression of Cerebral Amyloid Angiopathy. . 2023-02-00. Pubmed ID: 36689586; DOI: 10.1161/strokeaha.122.040823; PMC: PMC9855754 LUMCi005-A 2023-02-00 2023-02-00 PubMed: 36689586 DOI: 10.1161/strokeaha.122.040823Associated cell lines:
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Zhen S, Chen H, Lu J, Yang X, Tuo X, Chang S, Tian Y, Li X
Intravaginal delivery for CRISPR-Cas9 technology: For example, the treatment of HPV infection
Zhen S et al. Intravaginal delivery for CRISPR-Cas9 technology: For example, the treatment of HPV infection. . 2023-02-00. Pubmed ID: 36734062; DOI: 10.1002/jmv.28552 KSCBi005-AKSCBi005-A-5 2023-02-00 2023-02-00 PubMed: 36734062 DOI: 10.1002/jmv.28552Associated cell lines:
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Serpieri V, Orsi A, Mazzotta C, Cavan S, Rossi E, Scelsa B, Valente EM
Generation of an iPSC line from skin fibroblasts of a patient with Joubert syndrome carrying the homozygous loss of function variant c.787dupC in the AHI1 gene
Serpieri V et al. Generation of an iPSC line from skin fibroblasts of a patient with Joubert syndrome carrying the homozygous loss of function variant c.787dupC in the AHI1 gene. . 2023-02-00. Pubmed ID: 36521382; DOI: 10.1016/j.scr.2022.103002 UNIPVi001-A 2023-02-00 2023-02-00 PubMed: 36521382 DOI: 10.1016/j.scr.2022.103002Associated cell lines:
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Li L, Si X, Lei M, Yang J, Ruan J, Liu H, Huang F, Jin X, Xie K, Yang H, Lei X, Liu Y
Generation of a human iPSC line (CIBi013-A) from a patient with young-onset Parkinson's disease carrying a novel homozygous PARK7 (DJ-1) mutation
Li L et al. Generation of a human iPSC line (CIBi013-A) from a patient with young-onset Parkinson's disease carrying a novel homozygous PARK7 (DJ-1) mutation. . 2023-02-00. Pubmed ID: 36469984; DOI: 10.1016/j.scr.2022.102983 CIBi013-A 2023-02-00 2023-02-00 PubMed: 36469984 DOI: 10.1016/j.scr.2022.102983Associated cell lines:
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Wang Y, Fang Y, Wang Y, Xia S, Zhang D, An Q, Li Y, Luo S
Establishment of induced pluripotent stem cell lines from an ARVC patient carrying a heterozygous variant in LAMA2 gene
Wang Y et al. Establishment of induced pluripotent stem cell lines from an ARVC patient carrying a heterozygous variant in LAMA2 gene. . 2023-02-00. Pubmed ID: 36535090; DOI: 10.1016/j.scr.2022.102999 WCHi002-A 2023-02-00 2023-02-00 PubMed: 36535090 DOI: 10.1016/j.scr.2022.102999Associated cell lines:
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Yang L, Lu S, Yang Z, Yao J, Zhou P, Zhao M
Generation of an induced pluripotent stem cell line (IPCASi001-A) from an autism spectrum disorder individual without intellectual disability
Yang L et al. Generation of an induced pluripotent stem cell line (IPCASi001-A) from an autism spectrum disorder individual without intellectual disability. . 2023-02-00. Pubmed ID: 36502620; DOI: 10.1016/j.scr.2022.102994 IPCASi001-A 2023-02-00 2023-02-00 PubMed: 36502620 DOI: 10.1016/j.scr.2022.102994Associated cell lines:
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Mathews M, Wißfeld J, Flitsch LJ, Shahraz A, Semkova V, Breitkreuz Y, Neumann H, Brüstle O
Reenacting Neuroectodermal Exposure of Hematopoietic Progenitors Enables Scalable Production of Cryopreservable iPSC-Derived Human Microglia
Mathews M et al. Reenacting Neuroectodermal Exposure of Hematopoietic Progenitors Enables Scalable Production of Cryopreservable iPSC-Derived Human Microglia. . 2023-02-00. Pubmed ID: 35971018; DOI: 10.1007/s12015-022-10433-w; PMC: PMC9902330 BIONi010-C 2023-02-00 2023-02-00 PubMed: 35971018 DOI: 10.1007/s12015-022-10433-wAssociated cell lines:
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Popoiu TA, Dudek J, Maack C, Bertero E
Cardiac Involvement in Mitochondrial Disorders
Popoiu TA et al. Cardiac Involvement in Mitochondrial Disorders. . 2023-02-00. Pubmed ID: 36802007; DOI: 10.1007/s11897-023-00592-3; PMC: PMC9977856 LIBUCi001-ALIBUCi002-AJMUi001-AJMUi001-A-1 2023-02-00 2023-02-00 PubMed: 36802007 DOI: 10.1007/s11897-023-00592-3Associated cell lines:
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Peng T, Cheng Y, Xiong M, Cheng G
Generation of a human iPSC line (FDCHi009-A) from a patient with CHARGE syndrome carrying a novel CHD7 mutation (c.2939 T > C)
Peng T et al. Generation of a human iPSC line (FDCHi009-A) from a patient with CHARGE syndrome carrying a novel CHD7 mutation (c.2939 T > C). . 2023-02-00. Pubmed ID: 36502621; DOI: 10.1016/j.scr.2022.102996 FDCHi009-A 2023-02-00 2023-02-00 PubMed: 36502621 DOI: 10.1016/j.scr.2022.102996Associated cell lines:
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Xiang J, Huang N, Ouyang Q, Yi Y, Ding Y, An Y
Generation of an induced pluripotent stem cell line FDHPIi001-A derived from a female patient with WDR45-related neurodegeneration disease carrying non-canonical splice site c.344 + 5G > T
Xiang J et al. Generation of an induced pluripotent stem cell line FDHPIi001-A derived from a female patient with WDR45-related neurodegeneration disease carrying non-canonical splice site c.344 + 5G > T. . 2023-02-00. Pubmed ID: 36502619; DOI: 10.1016/j.scr.2022.102992 FDHPIi001-A 2023-02-00 2023-02-00 PubMed: 36502619 DOI: 10.1016/j.scr.2022.102992Associated cell lines:
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Khampang S, Jiamvoraphong N, Laowtammathron C, Lorthongpanich C, Klaihmon P, Srisook P, Kang X, Luanpitpong S, U-Pratya Y, Issaragrisil S
CRISPR/Cas9 mediated approach to generate YAP-depleted human embryonic stem cell line (MUSIe002-A-1)
Khampang S et al. CRISPR/Cas9 mediated approach to generate YAP-depleted human embryonic stem cell line (MUSIe002-A-1). . 2023-02-00. Pubmed ID: 36528979; DOI: 10.1016/j.scr.2022.102990 MUSIe002-AMUSIe002-A-1 2023-02-00 2023-02-00 PubMed: 36528979 DOI: 10.1016/j.scr.2022.102990Associated cell lines:
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Lattuada C, Santangelo S, Peverelli S, McGoldrick P, Rogaeva E, Zinman L, Haase G, Géli V, Silani V, Robertson J, Ratti A, Bossolasco P
Generation of five induced pluripotent stem cells lines from four members of the same family carrying a C9orf72 repeat expansion and one wild-type member
Lattuada C et al. Generation of five induced pluripotent stem cells lines from four members of the same family carrying a C9orf72 repeat expansion and one wild-type member. . 2023-02-00. Pubmed ID: 36528014; DOI: 10.1016/j.scr.2022.102998 IAIi005-AIAIi006-AIAIi007-AIAIi008-AIAIi009-A 2023-02-00 2023-02-00 PubMed: 36528014 DOI: 10.1016/j.scr.2022.102998 -
Vivekanandan R, Szepes M, Ricci Signorini ME, Kravchenko D, Kiefer J, Berger S, Fricke V, Göhring G, Gruh I
Generation of human induced pluripotent stem cell line encoding for a genetically encoded voltage indicator Arclight A242
Vivekanandan R et al. Generation of human induced pluripotent stem cell line encoding for a genetically encoded voltage indicator Arclight A242. . 2023-02-00. Pubmed ID: 36463634; DOI: 10.1016/j.scr.2022.102981 MHHi001-AMHHi001-A-10 2023-02-00 2023-02-00 PubMed: 36463634 DOI: 10.1016/j.scr.2022.102981Associated cell lines:
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Sieliwonczyk E, Alaerts M, Simons E, Snyders D, Nijak A, Vandendriessche B, Schepers D, Akdeniz D, Van Craenenbroeck E, Knaepen K, Rabaut L, Heidbuchel H, Van Laer L, Saenen J, Labro AJ, Loeys B
Clinical and functional characterisation of a recurrent KCNQ1 variant in the Belgian population
Sieliwonczyk E et al. Clinical and functional characterisation of a recurrent KCNQ1 variant in the Belgian population. . 2023-01-31. Pubmed ID: 36721196; DOI: 10.1186/s13023-023-02618-4; PMC: PMC9887867 PSMi007-A 2023-01-31 2023-01-31 PubMed: 36721196 DOI: 10.1186/s13023-023-02618-4Associated cell lines:
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Jiamvoraphong N, Septham P, Klaihmon P, Laowtammathron C, U-Pratya Y, Lorthongpanich C, Issaragrisil S
Derivation of MUSIi016-A iPSCs from peripheral blood with blood type O Rh positive
Jiamvoraphong N et al. Derivation of MUSIi016-A iPSCs from peripheral blood with blood type O Rh positive. . 2023-02-00. Pubmed ID: 36603353; DOI: 10.1016/j.scr.2022.103014 MUSIi016-A 2023-02-00 2023-02-00 PubMed: 36603353 DOI: 10.1016/j.scr.2022.103014Associated cell lines:
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Horschitz S, Frank J, Koch P
Generation of three induced pluripotent stem cell lines carrying different variants of the BDNF (Val66Met) polymorphism
Horschitz S et al. Generation of three induced pluripotent stem cell lines carrying different variants of the BDNF (Val66Met) polymorphism. . 2023-02-00. Pubmed ID: 36473250; DOI: 10.1016/j.scr.2022.102989 CIMHi001-ACIMHi004-ACIMHi005-A 2023-02-00 2023-02-00 PubMed: 36473250 DOI: 10.1016/j.scr.2022.102989Associated cell lines:
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Zhai Y, Miao J, Peng Y, Wang Y, Dong J, Zhao X
Clinical features of Danon disease and insights gained from LAMP-2 deficiency models
Zhai Y et al. Clinical features of Danon disease and insights gained from LAMP-2 deficiency models. . 2023-02-00. Pubmed ID: 34737089; DOI: 10.1016/j.tcm.2021.10.012 ZZUNEUi020-A 2023-02-00 2023-02-00 PubMed: 34737089 DOI: 10.1016/j.tcm.2021.10.012Associated cell lines:
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Li L, Si X, Yang J, Lei M, Liu H, Ruan J, Fu H, Li W, Yang H, Lei X, Sang H
Generation of a human iPSC line (CIBi014-A) from a patient with Parkinson's disease carrying a novel heterozygotic PARK8 (LRRK2) mutation
Li L et al. Generation of a human iPSC line (CIBi014-A) from a patient with Parkinson's disease carrying a novel heterozygotic PARK8 (LRRK2) mutation. . 2023-02-00. Pubmed ID: 36528012; DOI: 10.1016/j.scr.2022.102995 CIBi014-A 2023-02-00 2023-02-00 PubMed: 36528012 DOI: 10.1016/j.scr.2022.102995Associated cell lines:
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Guan M, Chai Y, Yi R, Chen Y, Ip JPK, Ye T, Chen Y
Generation of a homozygous ABCA7-knockout human iPSC line using the CRISPR/Cas9 system
Guan M et al. Generation of a homozygous ABCA7-knockout human iPSC line using the CRISPR/Cas9 system. . 2023-02-00. Pubmed ID: 36521383; DOI: 10.1016/j.scr.2022.103000 CNNDi001-ACNNDi001-A-1 2023-02-00 2023-02-00 PubMed: 36521383 DOI: 10.1016/j.scr.2022.103000Associated cell lines:
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De Kinderen P, Rabaut L, Hebert A, Ponsaerts P, Perik M, Meester JAN
Generation of an induced pluripotent stem cell (iPSC) line (BBANTWi009-A) from a Meester-Loeys syndrome patient carrying a BGN mutation
De Kinderen P et al. Generation of an induced pluripotent stem cell (iPSC) line (BBANTWi009-A) from a Meester-Loeys syndrome patient carrying a BGN mutation. . 2023-02-00. Pubmed ID: 36599284; DOI: 10.1016/j.scr.2022.103009 BBANTWi009-A 2023-02-00 2023-02-00 PubMed: 36599284 DOI: 10.1016/j.scr.2022.103009Associated cell lines:
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Loiben A, Friedman CE, Chien WM, Stempien-Otero A, Lin S, Yang KC
Generation of human iPSC line from an arrhythmogenic cardiomyopathy patient with a DSP protein-truncating variant
Loiben A et al. Generation of human iPSC line from an arrhythmogenic cardiomyopathy patient with a DSP protein-truncating variant. . 2023-02-00. Pubmed ID: 36481506; DOI: 10.1016/j.scr.2022.102987; PMC: PMC9900081 ISCRMi001-A 2023-02-00 2023-02-00 PubMed: 36481506 DOI: 10.1016/j.scr.2022.102987Associated cell lines:
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Yuan Yin X, Hua Zhu Z, Feng Chen R, Li J, Ya Zhang G, Long Hou W, Nan Zhuang N, Cai Y, Bin Dai N, Liu F, Wang J, Fang Jia Q, Hui L
Generation and characterization of iPSCs from a patient with obsessive-compulsive disorder, his mother with schizophrenia and his healthy father
Yuan Yin X et al. Generation and characterization of iPSCs from a patient with obsessive-compulsive disorder, his mother with schizophrenia and his healthy father. . 2023-02-00. Pubmed ID: 36502622; DOI: 10.1016/j.scr.2022.102993 SZGJMSi001-ASZGJMSi002-ASZGJMSi003-A 2023-02-00 2023-02-00 PubMed: 36502622 DOI: 10.1016/j.scr.2022.102993Associated cell lines:
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Sun H, Wang Z, Zhang Q, Chen N, Tang M, Yang Z, Xu Y, Kang J, Wang Y
Golgi damage caused by dysfunction of PiT-2 in primary familial brain calcification
Sun H et al. Golgi damage caused by dysfunction of PiT-2 in primary familial brain calcification. . 2023-01-29. Pubmed ID: 36584480; DOI: 10.1016/j.bbrc.2022.12.050 ZZUi019-AZZUi028-A 2023-01-29 2023-01-29 PubMed: 36584480 DOI: 10.1016/j.bbrc.2022.12.050 -
Kong D, Park KH, Kim DH, Kim NG, Lee SE, Shin N, Kook MG, Kim YB, Kang KS
Cortical-blood vessel assembloids exhibit Alzheimer's disease phenotypes by activating glia after SARS-CoV-2 infection
Kong D et al. Cortical-blood vessel assembloids exhibit Alzheimer's disease phenotypes by activating glia after SARS-CoV-2 infection. . 2023-01-25. Pubmed ID: 36697403; DOI: 10.1038/s41420-022-01288-8; PMC: PMC9876421 KSCBi005-A 2023-01-25 2023-01-25 PubMed: 36697403 DOI: 10.1038/s41420-022-01288-8Associated cell lines:
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Álvarez M, Ruiz-Sala P, Pérez B, Desviat LR, Richard E
Dysregulated Cell Homeostasis and miRNAs in Human iPSC-Derived Cardiomyocytes from a Propionic Acidemia Patient with Cardiomyopathy
Álvarez M et al. Dysregulated Cell Homeostasis and miRNAs in Human iPSC-Derived Cardiomyocytes from a Propionic Acidemia Patient with Cardiomyopathy. . 2023-01-22. Pubmed ID: 36768524; DOI: 10.3390/ijms24032182; PMC: PMC9916417 UAMi004-AUAMi004-A-1 2023-01-22 2023-01-22 PubMed: 36768524 DOI: 10.3390/ijms24032182Associated cell lines:
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Schoger E, Bleckwedel F, Germena G, Rocha C, Tucholla P, Sobitov I, Möbius W, Sitte M, Lenz C, Samak M, Hinkel R, Varga ZV, Giricz Z, Salinas G, Gross JC, Zelarayán LC
Single-cell transcriptomics reveal extracellular vesicles secretion with a cardiomyocyte proteostasis signature during pathological remodeling
Schoger E et al. Single-cell transcriptomics reveal extracellular vesicles secretion with a cardiomyocyte proteostasis signature during pathological remodeling. . 2023-01-21. Pubmed ID: 36681760; DOI: 10.1038/s42003-022-04402-9; PMC: PMC9867722 RUCDRi002-A 2023-01-21 2023-01-21 PubMed: 36681760 DOI: 10.1038/s42003-022-04402-9Associated cell lines:
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Gerasimova T, Stepanenko E, Novosadova L, Arsenyeva E, Shimchenko D, Tarantul V, Grivennikov I, Nenasheva V, Novosadova E
Glial Cultures Differentiated from iPSCs of Patients with PARK2-Associated Parkinson's Disease Demonstrate a Pro-Inflammatory Shift and Reduced Response to TNFα Stimulation
Gerasimova T et al. Glial Cultures Differentiated from iPSCs of Patients with PARK2-Associated Parkinson's Disease Demonstrate a Pro-Inflammatory Shift and Reduced Response to TNFα Stimulation. . 2023-01-19. Pubmed ID: 36768317; DOI: 10.3390/ijms24032000; PMC: PMC9916517 RCPCMi008-A 2023-01-19 2023-01-19 PubMed: 36768317 DOI: 10.3390/ijms24032000Associated cell lines:
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Feringa FM, van Berkel AA, Nair A, Verhage M
An Atypical, Staged Cell Death Pathway Induced by Depletion of SNARE-Proteins MUNC18-1 or Syntaxin-1
Feringa FM et al. An Atypical, Staged Cell Death Pathway Induced by Depletion of SNARE-Proteins MUNC18-1 or Syntaxin-1. . 2023-01-18. Pubmed ID: 36517239; DOI: 10.1523/jneurosci.0611-22.2022; PMC: PMC9864589 BIONi010-C-13 2023-01-18 2023-01-18 PubMed: 36517239 DOI: 10.1523/jneurosci.0611-22.2022Associated cell lines:
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Gerace D, Zhou Q, Kenty JH, Veres A, Sintov E, Wang X, Boulanger KR, Li H, Melton DA
Engineering human stem cell-derived islets to evade immune rejection and promote localized immune tolerance
Gerace D et al. Engineering human stem cell-derived islets to evade immune rejection and promote localized immune tolerance. . 2023-01-17. Pubmed ID: 36599351; DOI: 10.1016/j.xcrm.2022.100879; PMC: PMC9873825 HVRDe008-AHVRDe008-A-1 2023-01-17 2023-01-17 PubMed: 36599351 DOI: 10.1016/j.xcrm.2022.100879Associated cell lines:
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Gómez-Cabello D.
Erratum
Gómez-Cabello D.. Erratum. . 2023-01-17. DOI: 10.1159/000528841 FRIMOi007-A 2023-01-17 2023-01-17 DOI: 10.1159/000528841Associated cell lines:
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Stellon D, Talbot J, Hewitt AW, King AE, Cook AL
Seeing Neurodegeneration in a New Light Using Genetically Encoded Fluorescent Biosensors and iPSCs
Stellon D et al. Seeing Neurodegeneration in a New Light Using Genetically Encoded Fluorescent Biosensors and iPSCs. . 2023-01-16. Pubmed ID: 36675282; DOI: 10.3390/ijms24021766; PMC: PMC9861453 HIHRSi003-AHIHRSi003-A-1 2023-01-16 2023-01-16 PubMed: 36675282 DOI: 10.3390/ijms24021766Associated cell lines:
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Tamayo A, Núñez-Moreno G, Ruiz C, Plaisancie J, Damian A, Moya J, Chassaing N, Calvas P, Ayuso C, Minguez P, Corton M
Minigene Splicing Assays and Long-Read Sequencing to Unravel Pathogenic Deep-Intronic Variants in PAX6 in Congenital Aniridia
Tamayo A et al. Minigene Splicing Assays and Long-Read Sequencing to Unravel Pathogenic Deep-Intronic Variants in PAX6 in Congenital Aniridia. . 2023-01-13. Pubmed ID: 36675087; DOI: 10.3390/ijms24021562; PMC: PMC9863980 SDQLCHi010-AUCLi013-A 2023-01-13 2023-01-13 PubMed: 36675087 DOI: 10.3390/ijms24021562Associated cell lines:
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Katolikova NV, Khudiakov AA, Shafranskaya DD, Prjibelski AD, Masharskiy AE, Mor MS, Golovkin AS, Zaytseva AK, Neganova IE, Efimova EV, Gainetdinov RR, Malashicheva AB
Modulation of Notch Signaling at Early Stages of Differentiation of Human Induced Pluripotent Stem Cells to Dopaminergic Neurons
Katolikova NV et al. Modulation of Notch Signaling at Early Stages of Differentiation of Human Induced Pluripotent Stem Cells to Dopaminergic Neurons. . 2023-01-11. Pubmed ID: 36674941; DOI: 10.3390/ijms24021429; PMC: PMC9867149 WTSIi004-AWTSIi046-A 2023-01-11 2023-01-11 PubMed: 36674941 DOI: 10.3390/ijms24021429Associated cell lines:
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Huang G, Bisaria A, Wakefield DL, Yamawaki TM, Luo X, Zhang JA, Vigneault P, Wang J, Reagan JD, Oliverio O, Zhou H, Li CM, Vila OF, Wang S, Malik FI, Hartman JJ, Hale CM
Titin-truncating variants in hiPSC cardiomyocytes induce pathogenic proteinopathy and sarcomere defects with preserved core contractile machinery
Huang G et al. Titin-truncating variants in hiPSC cardiomyocytes induce pathogenic proteinopathy and sarcomere defects with preserved core contractile machinery. . 2023-01-10. Pubmed ID: 36525964; DOI: 10.1016/j.stemcr.2022.11.008; PMC: PMC9860080 TMOi001-A 2023-01-10 2023-01-10 PubMed: 36525964 DOI: 10.1016/j.stemcr.2022.11.008Associated cell lines:
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Schmidt M, Zeevaert K, Elsafi Mabrouk MH, Goetzke R, Wagner W
Epigenetic biomarkers to track differentiation of pluripotent stem cells
Schmidt M et al. Epigenetic biomarkers to track differentiation of pluripotent stem cells. . 2023-01-10. Pubmed ID: 36460001; DOI: 10.1016/j.stemcr.2022.11.001; PMC: PMC9860076 UKAi009-AUKAi010-AUKAi011-A 2023-01-10 2023-01-10 PubMed: 36460001 DOI: 10.1016/j.stemcr.2022.11.001 -
Wang HL, Ruan DD, Wu M, Ji YY, Hu XX, Wu QY, Zhang YP, Lin B, Hu YN, Wang H, Tang Y, Fang ZT, Luo JW, Liao LS, Gao MZ
Identification and characterization of two SERPINC1 mutations causing congenital antithrombin deficiency
Wang HL et al. Identification and characterization of two SERPINC1 mutations causing congenital antithrombin deficiency. . 2023-01-09. Pubmed ID: 36624481; DOI: 10.1186/s12959-022-00443-6; PMC: PMC9830717 ZZUNEUi014-A 2023-01-09 2023-01-09 PubMed: 36624481 DOI: 10.1186/s12959-022-00443-6Associated cell lines:
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Fernandes HJR, Kent JP, Bruntraeger M, Bassett AR, Koulman A, Metzakopian E, Snowden SG
Mitochondrial and Endoplasmic Reticulum Stress Trigger Triglyceride Accumulation in Models of Parkinson's Disease Independent of Mutations in MAPT
Fernandes HJR et al. Mitochondrial and Endoplasmic Reticulum Stress Trigger Triglyceride Accumulation in Models of Parkinson's Disease Independent of Mutations in MAPT. . 2023-01-09. Pubmed ID: 36677037; DOI: 10.3390/metabo13010112; PMC: PMC9861589 WTSIi018-BWTSIi018-B-1 2023-01-09 2023-01-09 PubMed: 36677037 DOI: 10.3390/metabo13010112Associated cell lines:
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Dutta B, Osato M
The RUNX Family, a Novel Multifaceted Guardian of the Genome
Dutta B et al. The RUNX Family, a Novel Multifaceted Guardian of the Genome. . 2023-01-07. Pubmed ID: 36672189; DOI: 10.3390/cells12020255; PMC: PMC9856552 WAe001-A-44 2023-01-07 2023-01-07 PubMed: 36672189 DOI: 10.3390/cells12020255Associated cell lines:
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Henkel LM, Kankowski S, Moellenkamp TM, Smandzich NJ, Schwarz S, Di Fonzo A, Göhring G, Höglinger G, Wegner F
iPSC-Derived Striatal Medium Spiny Neurons from Patients with Multiple System Atrophy Show Hypoexcitability and Elevated α-Synuclein Release
Henkel LM et al. iPSC-Derived Striatal Medium Spiny Neurons from Patients with Multiple System Atrophy Show Hypoexcitability and Elevated α-Synuclein Release. . 2023-01-04. Pubmed ID: 36672158; DOI: 10.3390/cells12020223; PMC: PMC9856678 UKWNLi002-A 2023-01-04 2023-01-04 PubMed: 36672158 DOI: 10.3390/cells12020223Associated cell lines:
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Duan Y, Lyu L, Zhan S
Stem Cell Therapy for Alzheimer's Disease: A Scoping Review for 2017-2022
Duan Y et al. Stem Cell Therapy for Alzheimer's Disease: A Scoping Review for 2017-2022. . 2023-01-03. Pubmed ID: 36672626; DOI: 10.3390/biomedicines11010120; PMC: PMC9855936 ZZUi009-ASIAISi003-A 2023-01-03 2023-01-03 PubMed: 36672626 DOI: 10.3390/biomedicines11010120Associated cell lines:
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Ruangrung K, Chakritbudsabong W, Thongon S, Rungarunlert S, Wattanapanitch M, Boonarkart C, Suptawiwat O, Sirinonthanawech N, Smith DR, Auewarakul P
Analysis of Influenza A virus infection in human induced pluripotent stem cells (hiPSCs) and their derivatives
Ruangrung K et al. Analysis of Influenza A virus infection in human induced pluripotent stem cells (hiPSCs) and their derivatives. . 2023-01-02. Pubmed ID: 36414188; DOI: 10.1016/j.virusres.2022.199009; PMC: PMC10194299 MUSIi001-A 2023-01-02 2023-01-02 PubMed: 36414188 DOI: 10.1016/j.virusres.2022.199009Associated cell lines:
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Guerrini R, Conti V, Mantegazza M, Balestrini S, Galanopoulou AS, Benfenati F
Developmental and epileptic encephalopathies: from genetic heterogeneity to phenotypic continuum
Guerrini R et al. Developmental and epileptic encephalopathies: from genetic heterogeneity to phenotypic continuum. . 2023-01-01. Pubmed ID: 35951482; DOI: 10.1152/physrev.00063.2021; PMC: PMC9576177 FUi002-A 2023-01-01 2023-01-01 PubMed: 35951482 DOI: 10.1152/physrev.00063.2021Associated cell lines:
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Stolzenburg L, Esmaeeli S, Kulkarni A, Murphy E, Kwon T, Preiss C, Bahnassawy L, Stender J, Manos J, Reinhardt P, Rahimov F, Waring J, Ramathal C.
Functional characterization of a single nucleotide polymorphism associated with Alzheimer’s disease in a hiPSC-based neuron model
Stolzenburg L et al. Functional characterization of a single nucleotide polymorphism associated with Alzheimer’s disease in a hiPSC-based neuron model. . 2023-01-01. BIONi010-CBIONi010-C-13 2023-01-01 2023-01-01Associated cell lines:
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Soldati S, Bär A, Vladymyrov M, Glavin D, McGrath J, Gosselet F, Nishihara H, Goelz S, Engelhardt B.
High levels of endothelial ICAM-1 prohibit natalizumab mediated abrogation of CD4+ T cell arrest on the inflamed BBB under flow in vitro
Soldati S et al. High levels of endothelial ICAM-1 prohibit natalizumab mediated abrogation of CD4+ T cell arrest on the inflamed BBB under flow in vitro. . 2023-01-01. LNISi002-BLNISi007-B 2023-01-01 2023-01-01Associated cell lines:
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Yao X.
Glomerulopathy with fibronectin deposits: a clinicopathological study
Yao X.. Glomerulopathy with fibronectin deposits: a clinicopathological study. . 2023-01-01. DOI: 10.3760/cma.j.cn112151-20230322-00218 FHUSTCi001-A 2023-01-01 2023-01-01 DOI: 10.3760/cma.j.cn112151-20230322-00218Associated cell lines:
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Chapotte-Baldacci C, Pierre M, Djemai M, Pouliot V, Chahine M.
Biophysical properties of NaV1.5 channels from atrial-like and ventricular-like cardiomyocytes derived from human induced pluripotent stem cells
Chapotte-Baldacci C et al. Biophysical properties of NaV1.5 channels from atrial-like and ventricular-like cardiomyocytes derived from human induced pluripotent stem cells. . 2023-01-01. CBRCULi001-ACBRCULi008-A 2023-01-01 2023-01-01Associated cell lines:
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Martínez-Puente DH, Garza-Morales R, Pérez-Trujillo JJ, Bernabé-Acosta F, Villanueva-Olivo A, García-García A, Zavala-Flores LM, Rodríguez-Rocha H, Valdés J, Saucedo-Cárdenas O, Montes de Oca-Luna R, Loera-Arias MJ
Enhanced antitumor activity induced by a DNA vaccine encoding E7 antigen fused to an ERAD-targeting sequence
Martínez-Puente DH et al. Enhanced antitumor activity induced by a DNA vaccine encoding E7 antigen fused to an ERAD-targeting sequence. . 2023-01-00. Pubmed ID: 35896308; DOI: 10.1080/1061186x.2022.2107651 SHIPMi001-ASHIPMi002-A 2023-01-00 2023-01-00 PubMed: 35896308 DOI: 10.1080/1061186x.2022.2107651Associated cell lines:
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Yui H, Otawa S, Horiuchi S, Kushima M, Shinohara R, Kojima R, Akiyama Y, Ooka T, Miyake K, Yokomichi H, Yamagata Z, Yamanashi Adjunct Study of the Japan Environment and Children's Study Group
Appropriate procedures to increase the adherence of children to blood collection: A cross-sectional study
Yui H et al. Appropriate procedures to increase the adherence of children to blood collection: A cross-sectional study. . 2023-01-00. Pubmed ID: 36620513; DOI: 10.1002/hsr2.1036; PMC: PMC9798851 CSSi004-A 2023-01-00 2023-01-00 PubMed: 36620513 DOI: 10.1002/hsr2.1036Associated cell lines:
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Tristan CA, Hong H, Jethmalani Y, Chen Y, Weber C, Chu PH, Ryu S, Jovanovic VM, Hur I, Voss TC, Simeonov A, Singeç I
Efficient and safe single-cell cloning of human pluripotent stem cells using the CEPT cocktail
Tristan CA et al. Efficient and safe single-cell cloning of human pluripotent stem cells using the CEPT cocktail. . 2023-01-00. Pubmed ID: 36261632; DOI: 10.1038/s41596-022-00753-z; PMC: PMC11009857 WAe001-AWAe007-AWAe009-ARUCDRi002-AUCSFi001-A 2023-01-00 2023-01-00 PubMed: 36261632 DOI: 10.1038/s41596-022-00753-zAssociated cell lines:
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Antarianto RD, Pragiwaksana A, Septiana WL, Mazfufah NF, Mahmood A
Hepatocyte Differentiation from iPSCs or MSCs in Decellularized Liver Scaffold: Cell-ECM Adhesion, Spatial Distribution, and Hepatocyte Maturation Profile
Antarianto RD et al. Hepatocyte Differentiation from iPSCs or MSCs in Decellularized Liver Scaffold: Cell-ECM Adhesion, Spatial Distribution, and Hepatocyte Maturation Profile. . 2022-12-31. Pubmed ID: 35435152; DOI: 10.1080/15476278.2022.2061263; PMC: PMC9037523 UKKi006-A 2022-12-31 2022-12-31 PubMed: 35435152 DOI: 10.1080/15476278.2022.2061263Associated cell lines:
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Lian TY, Yan Y, Ding D, Ma YJ, Zhang X, Jing ZC
Building a modern six-dimensional biobank fosters the future of precision medicine
Lian TY et al. Building a modern six-dimensional biobank fosters the future of precision medicine. . 2022-12-31. Pubmed ID: 36604021; DOI: 10.1016/j.scib.2022.12.002 PUMCHi003-APUMCHi006-A 2022-12-31 2022-12-31 PubMed: 36604021 DOI: 10.1016/j.scib.2022.12.002Associated cell lines:
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Angulo MB, Bertalovitz A, Argenziano MA, Yang J, Patel A, Zesiewicz T, McDonald TV
Frataxin deficiency alters gene expression in Friedreich ataxia derived IPSC-neurons and cardiomyocytes
Angulo MB et al. Frataxin deficiency alters gene expression in Friedreich ataxia derived IPSC-neurons and cardiomyocytes. . 2023-01-00. Pubmed ID: 36369844; DOI: 10.1002/mgg3.2093; PMC: PMC9834160 USFi001-A 2023-01-00 2023-01-00 PubMed: 36369844 DOI: 10.1002/mgg3.2093Associated cell lines:
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Chong ZS, Khong ZJ, Tay SH, Ng SY
Metabolic contributions to neuronal deficits caused by genomic disruption of schizophrenia risk gene SETD1A
Chong ZS et al. Metabolic contributions to neuronal deficits caused by genomic disruption of schizophrenia risk gene SETD1A. . 2022-12-29. Pubmed ID: 36581615; DOI: 10.1038/s41537-022-00326-9; PMC: PMC9800576 WAe007-A 2022-12-29 2022-12-29 PubMed: 36581615 DOI: 10.1038/s41537-022-00326-9Associated cell lines:
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Barndt RJ, Liu Q, Tang Y, Haugh MP, Cui J, Chan SY, Wu H
Metabolic Maturation Exaggerates Abnormal Calcium Handling in a Lamp2 Knockout Human Pluripotent Stem Cell-Derived Cardiomyocyte Model of Danon Disease
Barndt RJ et al. Metabolic Maturation Exaggerates Abnormal Calcium Handling in a Lamp2 Knockout Human Pluripotent Stem Cell-Derived Cardiomyocyte Model of Danon Disease. . 2022-12-29. Pubmed ID: 36671453; DOI: 10.3390/biom13010069; PMC: PMC9855424 UPITTi002-AUPITTi002-A-1 2022-12-29 2022-12-29 PubMed: 36671453 DOI: 10.3390/biom13010069Associated cell lines:
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Chirico N, Kessler EL, Maas RGC, Fang J, Qin J, Dokter I, Daniels M, Šarić T, Neef K, Buikema JW, Lei Z, Doevendans PA, Sluijter JPG, van Mil A
Small molecule-mediated rapid maturation of human induced pluripotent stem cell-derived cardiomyocytes
Chirico N et al. Small molecule-mediated rapid maturation of human induced pluripotent stem cell-derived cardiomyocytes. . 2022-12-27. Pubmed ID: 36575473; DOI: 10.1186/s13287-022-03209-z; PMC: PMC9795728 UKKi032-CUKKi036-CUKKi037-C 2022-12-27 2022-12-27 PubMed: 36575473 DOI: 10.1186/s13287-022-03209-z -
Lenzini L, Iori E, Scannapieco F, Carraro G, Avogaro A, Vitturi N
Urine-Derived Epithelial Cells as a New Model to Study Renal Metabolic Phenotypes of Patients with Glycogen Storage Disease 1a
Lenzini L et al. Urine-Derived Epithelial Cells as a New Model to Study Renal Metabolic Phenotypes of Patients with Glycogen Storage Disease 1a. . 2022-12-23. Pubmed ID: 36613675; DOI: 10.3390/ijms24010232; PMC: PMC9820562 BRCi009-A 2022-12-23 2022-12-23 PubMed: 36613675 DOI: 10.3390/ijms24010232Associated cell lines:
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Ho BX, Pang JKS, Chen Y, Loh YH, An O, Yang HH, Seshachalam VP, Koh JLY, Chan WK, Ng SY, Soh BS
Robust generation of human-chambered cardiac organoids from pluripotent stem cells for improved modelling of cardiovascular diseases
Ho BX et al. Robust generation of human-chambered cardiac organoids from pluripotent stem cells for improved modelling of cardiovascular diseases. . 2022-12-21. Pubmed ID: 36544188; DOI: 10.1186/s13287-022-03215-1; PMC: PMC9773542 WAe007-A 2022-12-21 2022-12-21 PubMed: 36544188 DOI: 10.1186/s13287-022-03215-1Associated cell lines:
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Kogler S, Aizenshtadt A, Harrison S, Skottvoll FS, Berg HE, Abadpour S, Scholz H, Sullivan G, Thiede B, Lundanes E, Bogen IL, Krauss S, Røberg-Larsen H, Wilson SR
"Organ-in-a-Column" Coupled On-line with Liquid Chromatography-Mass Spectrometry
Kogler S et al. "Organ-in-a-Column" Coupled On-line with Liquid Chromatography-Mass Spectrometry. . 2022-12-20. Pubmed ID: 36484723; DOI: 10.1021/acs.analchem.2c04530; PMC: PMC9773175 WTSIi013-AWTSIi028-A 2022-12-20 2022-12-20 PubMed: 36484723 DOI: 10.1021/acs.analchem.2c04530Associated cell lines:
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de Graaf MNS, Vivas A, Kasi DG, van den Hil FE, van den Berg A, van der Meer AD, Mummery CL, Orlova VV
Multiplexed fluidic circuit board for controlled perfusion of 3D blood vessels-on-a-chip
de Graaf MNS et al. Multiplexed fluidic circuit board for controlled perfusion of 3D blood vessels-on-a-chip. . 2022-12-20. Pubmed ID: 36484766; DOI: 10.1039/d2lc00686c; PMC: PMC9764810 UCSFi001-AUCSFi001-A-2 2022-12-20 2022-12-20 PubMed: 36484766 DOI: 10.1039/d2lc00686cAssociated cell lines:
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Rosselot AE, Park M, Kim M, Matsu-Ura T, Wu G, Flores DE, Subramanian KR, Lee S, Sundaram N, Broda TR, McCauley HA, Hawkins JA, Chetal K, Salomonis N, Shroyer NF, Helmrath MA, Wells JM, Hogenesch JB, Moore SR, Hong CI
Ontogeny and function of the circadian clock in intestinal organoids
Rosselot AE et al. Ontogeny and function of the circadian clock in intestinal organoids. . 2022-12-17. Pubmed ID: 34704277; DOI: 10.15252/embj.2020106973; PMC: PMC8762567 CUSTOMi001-A 2022-12-17 2022-12-17 PubMed: 34704277 DOI: 10.15252/embj.2020106973Associated cell lines:
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Hübschmann V, Korkut-Demirbaş M, Siegert S
Assessing human iPSC-derived microglia identity and function by immunostaining, phagocytosis, calcium activity, and inflammation assay
Hübschmann V et al. Assessing human iPSC-derived microglia identity and function by immunostaining, phagocytosis, calcium activity, and inflammation assay. . 2022-12-16. Pubmed ID: 36595902; DOI: 10.1016/j.xpro.2022.101866; PMC: PMC9678782 CRMi001-A 2022-12-16 2022-12-16 PubMed: 36595902 DOI: 10.1016/j.xpro.2022.101866Associated cell lines:
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Klepikova A, Nenasheva T, Sheveleva O, Protasova E, Antonov D, Gainullina A, Chikina E, Sakovnich O, Gerasimova T, Nikitina I, Shevalie D, Lyadova I
iPSC-Derived Macrophages: The Differentiation Protocol Affects Cell Immune Characteristics and Differentiation Trajectories
Klepikova A et al. iPSC-Derived Macrophages: The Differentiation Protocol Affects Cell Immune Characteristics and Differentiation Trajectories. . 2022-12-16. Pubmed ID: 36555728; DOI: 10.3390/ijms232416087; PMC: PMC9781144 ICGi021-AICGi022-A 2022-12-16 2022-12-16 PubMed: 36555728 DOI: 10.3390/ijms232416087 -
Caillaud A, Lévêque A, Thédrez A, Girardeau A, Canac R, Bray L, Baudic M, Barc J, Gaborit N, Lamirault G, Gardie B, Idriss S, Rimbert A, Le May C, Cariou B, Si-Tayeb K
FACS-assisted CRISPR-Cas9 genome editing of human induced pluripotent stem cells
Caillaud A et al. FACS-assisted CRISPR-Cas9 genome editing of human induced pluripotent stem cells. . 2022-12-16. Pubmed ID: 36115027; DOI: 10.1016/j.xpro.2022.101680; PMC: PMC9490201 ITXi001-AITXi001-A-1ITXi002-AITXi002-A-3 2022-12-16 2022-12-16 PubMed: 36115027 DOI: 10.1016/j.xpro.2022.101680Associated cell lines:
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Surendran H, Soundararajan L, Reddy K VB, Subramani J, Stoddard J, Reynaga R, Tschetter W, Ryals RC, Pal R
An improved protocol for generation and characterization of human-induced pluripotent stem cell-derived retinal pigment epithelium cells
Surendran H et al. An improved protocol for generation and characterization of human-induced pluripotent stem cell-derived retinal pigment epithelium cells. . 2022-12-16. Pubmed ID: 36386870; DOI: 10.1016/j.xpro.2022.101803; PMC: PMC9641055 ERPLi001-AERPLi002-AERPLi003-A 2022-12-16 2022-12-16 PubMed: 36386870 DOI: 10.1016/j.xpro.2022.101803Associated cell lines:
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Fuchs S, van Helden RWJ, Wiendels M, de Graaf MNS, Orlova VV, Mummery CL, van Meer BJ, Mayr T
On-chip analysis of glycolysis and mitochondrial respiration in human induced pluripotent stem cells
Fuchs S et al. On-chip analysis of glycolysis and mitochondrial respiration in human induced pluripotent stem cells. . 2022-12-15. Pubmed ID: 36388452; DOI: 10.1016/j.mtbio.2022.100475; PMC: PMC9647220 LUMCi028-A 2022-12-15 2022-12-15 PubMed: 36388452 DOI: 10.1016/j.mtbio.2022.100475Associated cell lines:
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Waldhorn I, Turetsky T, Steiner D, Gil Y, Benyamini H, Gropp M, Reubinoff BE
Modeling sex differences in humans using isogenic induced pluripotent stem cells
Waldhorn I et al. Modeling sex differences in humans using isogenic induced pluripotent stem cells. . 2022-12-13. Pubmed ID: 36427492; DOI: 10.1016/j.stemcr.2022.10.017; PMC: PMC9768579 KAUSTi006-AKAUSTi006-B 2022-12-13 2022-12-13 PubMed: 36427492 DOI: 10.1016/j.stemcr.2022.10.017Associated cell lines:
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Yang W, Chen L, Guo J, Shi F, Yang Q, Xie L, Lu D, Li Y, Luo J, Wang L, Qiu L, Chen T, Li Y, Zhang R, Chen L, Xu W, Liu H
Multiomics Analysis of a DNAH5-Mutated PCD Organoid Model Revealed the Key Role of the TGF-β/BMP and Notch Pathways in Epithelial Differentiation and the Immune Response in DNAH5-Mutated Patients
Yang W et al. Multiomics Analysis of a DNAH5-Mutated PCD Organoid Model Revealed the Key Role of the TGF-β/BMP and Notch Pathways in Epithelial Differentiation and the Immune Response in DNAH5-Mutated Patients. . 2022-12-12. Pubmed ID: 36552777; DOI: 10.3390/cells11244013; PMC: PMC9776854 MHHi017-AMHHi017-B 2022-12-12 2022-12-12 PubMed: 36552777 DOI: 10.3390/cells11244013 -
Lee JJ, Lin CY, Chen HC, Hsieh PCH, Chiu YW, Chang JM
Opportunities and Challenges of Human IPSC Technology in Kidney Disease Research
Lee JJ et al. Opportunities and Challenges of Human IPSC Technology in Kidney Disease Research. . 2022-12-12. Pubmed ID: 36551987; DOI: 10.3390/biomedicines10123232; PMC: PMC9775669 MUi027-A 2022-12-12 2022-12-12 PubMed: 36551987 DOI: 10.3390/biomedicines10123232Associated cell lines:
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Mahato S, Agrawal T, Pidishetty D, Maddileti S, Pulimamidi VK, Mariappan I
Generation of Retinal Organoids from Healthy and Retinal Disease-Specific Human-Induced Pluripotent Stem Cells
Mahato S et al. Generation of Retinal Organoids from Healthy and Retinal Disease-Specific Human-Induced Pluripotent Stem Cells. . 2022-12-09. Pubmed ID: 36571401; DOI: 10.3791/64509 LVPEIi001-A 2022-12-09 2022-12-09 PubMed: 36571401 DOI: 10.3791/64509Associated cell lines:
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Wang H, Krause A, Escobar H, Müthel S, Metzler E, Spuler S
LMNA Co-Regulated Gene Expression as a Suitable Readout after Precise Gene Correction
Wang H et al. LMNA Co-Regulated Gene Expression as a Suitable Readout after Precise Gene Correction. . 2022-12-08. Pubmed ID: 36555163; DOI: 10.3390/ijms232415525; PMC: PMC9778678 MDCi011-AMDCi011-BMDCi012-AMDCi012-BMDCi013-AMDCi013-BMDCi014-AMDCi014-B 2022-12-08 2022-12-08 PubMed: 36555163 DOI: 10.3390/ijms232415525 -
Crouzier L, Richard EM, Diez C, Denus M, Peyrel A, Alzaeem H, Cubedo N, Delaunay T, Maurice T, Delprat B
NCS1 overexpression restored mitochondrial activity and behavioral alterations in a zebrafish model of Wolfram syndrome
Crouzier L et al. NCS1 overexpression restored mitochondrial activity and behavioral alterations in a zebrafish model of Wolfram syndrome. . 2022-12-08. Pubmed ID: 36320410; DOI: 10.1016/j.omtm.2022.10.003; PMC: PMC9594121 IMBPASi001-A 2022-12-08 2022-12-08 PubMed: 36320410 DOI: 10.1016/j.omtm.2022.10.003Associated cell lines:
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Javaid MS, Tan T, Dvir N, Anderson A, J O'Brien T, Kwan P, Antonic-Baker A
Human In Vitro Models of Epilepsy Using Embryonic and Induced Pluripotent Stem Cells
Javaid MS et al. Human In Vitro Models of Epilepsy Using Embryonic and Induced Pluripotent Stem Cells. . 2022-12-07. Pubmed ID: 36552721; DOI: 10.3390/cells11243957; PMC: PMC9776452 FUi002-AHIHDNEi002-ACSSi009-ACSSi010-AKICRi002-AKICRi002-A-3USTCi001-ANUIGi052-ANUIGi052-BNUIGi052-CUSTCi001-A-1GZHMCi001-AGZHMCi001-B 2022-12-07 2022-12-07 PubMed: 36552721 DOI: 10.3390/cells11243957Associated cell lines:
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Chien Y, Hsiao YJ, Chou SJ, Lin TY, Yarmishyn AA, Lai WY, Lee MS, Lin YY, Lin TW, Hwang DK, Lin TC, Chiou SH, Chen SJ, Yang YP
Nanoparticles-mediated CRISPR-Cas9 gene therapy in inherited retinal diseases: applications, challenges, and emerging opportunities
Chien Y et al. Nanoparticles-mediated CRISPR-Cas9 gene therapy in inherited retinal diseases: applications, challenges, and emerging opportunities. . 2022-12-03. Pubmed ID: 36463195; DOI: 10.1186/s12951-022-01717-x; PMC: PMC9719668 INMi003-A 2022-12-03 2022-12-03 PubMed: 36463195 DOI: 10.1186/s12951-022-01717-xAssociated cell lines:
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Brodehl A, Holler S, Gummert J, Milting H
The N-Terminal Part of the 1A Domain of Desmin Is a Hot Spot Region for Putative Pathogenic DES Mutations Affecting Filament Assembly
Brodehl A et al. The N-Terminal Part of the 1A Domain of Desmin Is a Hot Spot Region for Putative Pathogenic DES Mutations Affecting Filament Assembly. . 2022-12-02. Pubmed ID: 36497166; DOI: 10.3390/cells11233906; PMC: PMC9738904 UKKi011-A 2022-12-02 2022-12-02 PubMed: 36497166 DOI: 10.3390/cells11233906Associated cell lines:
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Faustini G, Longhena F, Muscò A, Bono F, Parrella E, La Via L, Barbon A, Pizzi M, Onofri F, Benfenati F, Missale C, Memo M, Zizioli D, Bellucci A
Synapsin III Regulates Dopaminergic Neuron Development in Vertebrates
Faustini G et al. Synapsin III Regulates Dopaminergic Neuron Development in Vertebrates. . 2022-12-02. Pubmed ID: 36497160; DOI: 10.3390/cells11233902; PMC: PMC9739466 UNIBSi014-A 2022-12-02 2022-12-02 PubMed: 36497160 DOI: 10.3390/cells11233902Associated cell lines:
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Pantazis CB, Yang A, Lara E, McDonough JA, Blauwendraat C, Peng L, Oguro H, Kanaujiya J, Zou J, Sebesta D, Pratt G, Cross E, Blockwick J, Buxton P, Kinner-Bibeau L, Medura C, Tompkins C, Hughes S, Santiana M, Faghri F, Nalls MA, Vitale D, Ballard S, Qi YA, Ramos DM, Anderson KM, Stadler J, Narayan P, Papademetriou J, Reilly L, Nelson MP, Aggarwal S, Rosen LU, Kirwan P, Pisupati V, Coon SL, Scholz SW, Priebe T, Öttl M, Dong J, Meijer M, Janssen LJM, Lourenco VS, van der Kant R, Crusius D, Paquet D, Raulin AC, Bu G, Held A, Wainger BJ, Gabriele RMC, Casey JM, Wray S, Abu-Bonsrah D, Parish CL, Beccari MS, Cleveland DW, Li E, Rose IVL, Kampmann M, Calatayud Aristoy C, Verstreken P, Heinrich L, Chen MY, Schüle B, Dou D, Holzbaur ELF, Zanellati MC, Basundra R, Deshmukh M, Cohen S, Khanna R, Raman M, Nevin ZS, Matia M, Van Lent J, Timmerman V, Conklin BR, Johnson Chase K, Zhang K, Funes S, Bosco DA, Erlebach L, Welzer M, Kronenberg-Versteeg D, Lyu G, Arenas E, Coccia E, Sarrafha L, Ahfeldt T, Marioni JC, Skarnes WC, Cookson MR, Ward ME, Merkle FT
A reference human induced pluripotent stem cell line for large-scale collaborative studies
Pantazis CB et al. A reference human induced pluripotent stem cell line for large-scale collaborative studies. . 2022-12-01. Pubmed ID: 36459969; DOI: 10.1016/j.stem.2022.11.004; PMC: PMC9782786 CRMi001-ACRMi003-ABIONi010-CWTSIi018-B-1BIONi010-C-13HVRDi004-BWTSIi018-B-12 2022-12-01 2022-12-01 PubMed: 36459969 DOI: 10.1016/j.stem.2022.11.004Associated cell lines:
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Wang T, Liu J, Chen J, Qin B
Generation and Differentiation of Induced Pluripotent Stem Cells from Mononuclear Cells in An Age-Related Macular Degeneration Patient
Wang T et al. Generation and Differentiation of Induced Pluripotent Stem Cells from Mononuclear Cells in An Age-Related Macular Degeneration Patient. . 2022-12-01. Pubmed ID: 36527349; DOI: 10.22074/cellj.2022.557559.1072; PMC: PMC9790072 CABi003-A 2022-12-01 2022-12-01 PubMed: 36527349 DOI: 10.22074/cellj.2022.557559.1072Associated cell lines:
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Beck Bodo B., Martin-Higueras Cristina, Hoppe Bernd
Primary Hyperoxaluria
Beck Bodo B. et al. Primary Hyperoxaluria. . 2023-00-00. DOI: 10.1007/978-3-031-11665-0_29 CIMAi001-A 2023-00-00 2023-00-00 DOI: 10.1007/978-3-031-11665-0_29Associated cell lines:
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Ortner Nadine J.
CACNA1D-Related Channelopathies: From Hypertension to Autism
Ortner Nadine J.. CACNA1D-Related Channelopathies: From Hypertension to Autism. . 2023-00-00. DOI: 10.1007/164_2022_626 IBKMOLi002-A 2023-00-00 2023-00-00 DOI: 10.1007/164_2022_626Associated cell lines:
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Pohl GM, Göz M, Gaertner A, Brodehl A, Cimen T, Saguner AM, Schulze-Bahr E, Walhorn V, Anselmetti D, Milting H
Cardiomyopathy related desmocollin-2 prodomain variants affect the intracellular cadherin transport and processing
Pohl GM et al. Cardiomyopathy related desmocollin-2 prodomain variants affect the intracellular cadherin transport and processing. . 2023-00-00. Pubmed ID: 37273868; DOI: 10.3389/fcvm.2023.1127261; PMC: PMC10235514 UKKi011-A 2023-00-00 2023-00-00 PubMed: 37273868 DOI: 10.3389/fcvm.2023.1127261Associated cell lines:
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Devito LG, Cooper F, D'Angelo I, Smith J, Healy L
Generation of FOUR iPSC lines (CRICKi004-A; CRICKi005-A; CRICKi006-A, CRICKi007-A) from Spinal muscle atrophy patients with lower extremity dominant (SMALED) phenotype
Devito LG et al. Generation of FOUR iPSC lines (CRICKi004-A; CRICKi005-A; CRICKi006-A, CRICKi007-A) from Spinal muscle atrophy patients with lower extremity dominant (SMALED) phenotype. . 2022-12-00. Pubmed ID: 36332468; DOI: 10.1016/j.scr.2022.102954 CRICKi001-ACRICKi004-ACRICKi005-ACRICKi006-ACRICKi007-A 2022-12-00 2022-12-00 PubMed: 36332468 DOI: 10.1016/j.scr.2022.102954Associated cell lines:
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Zhou L, Xu H, Wu Y, Fang F
Generation of a human iPSC line BCHNCi001-A from a patient with uridine-responsive epileptic encephalopathy carrying biallelic CAD mutations
Zhou L et al. Generation of a human iPSC line BCHNCi001-A from a patient with uridine-responsive epileptic encephalopathy carrying biallelic CAD mutations. . 2022-12-00. Pubmed ID: 36283272; DOI: 10.1016/j.scr.2022.102947 BCHNEi001-ACIPi001-ABCHNCi001-A 2022-12-00 2022-12-00 PubMed: 36283272 DOI: 10.1016/j.scr.2022.102947Associated cell lines:
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Heaton ES, Jin S
Importance of multiple endocrine cell types in islet organoids for type 1 diabetes treatment
Heaton ES et al. Importance of multiple endocrine cell types in islet organoids for type 1 diabetes treatment. . 2022-12-00. Pubmed ID: 35772687; DOI: 10.1016/j.trsl.2022.06.014; PMC: PMC11554285 KSCBi005-AKSCBi005-A-3 2022-12-00 2022-12-00 PubMed: 35772687 DOI: 10.1016/j.trsl.2022.06.014Associated cell lines:
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Takada K, Nakatani R, Moribe E, Yamazaki-Fujigaki S, Fujii M, Furuta M, Suemori H, Kawase E
Efficient derivation and banking of clinical-grade human embryonic stem cell lines in accordance with Japanese regulations
Takada K et al. Efficient derivation and banking of clinical-grade human embryonic stem cell lines in accordance with Japanese regulations. . 2022-12-00. Pubmed ID: 36397823; DOI: 10.1016/j.reth.2022.10.006; PMC: PMC9647332 KUIMSe004-AKUIMSe005-AKUIMSe006-AKUIMSe007-AKUIMSe008-AKUIMSe009-A 2022-12-00 2022-12-00 PubMed: 36397823 DOI: 10.1016/j.reth.2022.10.006Associated cell lines:
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Hadji Anya, Louit Aurélie, Roy Vincent, Blais Mathieu, Berthod François, Gros-Louis François, Dupré Nicolas
Autosomal and X-Linked Degenerative Ataxias: From Genetics to Promising Therapeutics
Hadji Anya et al. Autosomal and X-Linked Degenerative Ataxias: From Genetics to Promising Therapeutics. . 2023-00-00. DOI: 10.1007/978-3-031-24345-5_5 JUCTCi002-A 2023-00-00 2023-00-00 DOI: 10.1007/978-3-031-24345-5_5Associated cell lines:
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Kaneski CR, Hanover JA, Schueler Hoffman UH
Generation of GLA-knockout human embryonic stem cell lines to model peripheral neuropathy in Fabry disease
Kaneski CR et al. Generation of GLA-knockout human embryonic stem cell lines to model peripheral neuropathy in Fabry disease. . 2022-12-00. Pubmed ID: 36092250; DOI: 10.1016/j.ymgmr.2022.100914; PMC: PMC9449667 UKWNLi001-AINSAi002-ACMCi006-ACMCi007-AZJUi007-A 2022-12-00 2022-12-00 PubMed: 36092250 DOI: 10.1016/j.ymgmr.2022.100914Associated cell lines:
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Carido M, Völkner M, Steinheuer LM, Wagner F, Kurth T, Dumler N, Ulusoy S, Wieneke S, Norniella AV, Golfieri C, Khattak S, Schönfelder B, Scamozzi M, Zoschke K, Canzler S, Hackermüller J, Ader M, Karl MO
Reliability of human retina organoid generation from hiPSC-derived neuroepithelial cysts
Carido M et al. Reliability of human retina organoid generation from hiPSC-derived neuroepithelial cysts. . 2023-00-00. Pubmed ID: 37868194; DOI: 10.3389/fncel.2023.1166641; PMC: PMC10587494 CRTDi003-B 2023-00-00 2023-00-00 PubMed: 37868194 DOI: 10.3389/fncel.2023.1166641Associated cell lines:
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Ranjbarnejad F, Khazaei M, Shahryari A, Khazaei F, Rezakhani L
Recent advances in gene therapy for bone tissue engineering
Ranjbarnejad F et al. Recent advances in gene therapy for bone tissue engineering. . 2022-12-00. Pubmed ID: 36382408; DOI: 10.1002/term.3363 HMGUi001-AHMGUi001-A-5 2022-12-00 2022-12-00 PubMed: 36382408 DOI: 10.1002/term.3363Associated cell lines:
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De Bortoli M, Meraviglia V, Mackova K, Frommelt LS, König E, Rainer J, Volani C, Benzoni P, Schlittler M, Cattelan G, Motta BM, Volpato C, Rauhe W, Barbuti A, Zacchigna S, Pramstaller PP, Rossini A
Modeling incomplete penetrance in arrhythmogenic cardiomyopathy by human induced pluripotent stem cell derived cardiomyocytes
De Bortoli M et al. Modeling incomplete penetrance in arrhythmogenic cardiomyopathy by human induced pluripotent stem cell derived cardiomyocytes. . 2023-00-00. Pubmed ID: 36915380; DOI: 10.1016/j.csbj.2023.02.029; PMC: PMC10006475 EURACi007-AEURACi008-AEURACi009-A 2023-00-00 2023-00-00 PubMed: 36915380 DOI: 10.1016/j.csbj.2023.02.029Associated cell lines:
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Kamand M, Hohmann S, Louise Forsberg S, Thomassen M, Ilieva M, Fex Svenningsen Å, Meyer M, Maria Michel T
Generation and characterization of induced pluripotent stem (iPS) cell line (SDUCTi001-A) using fibroblasts derived from male-healthy donor
Kamand M et al. Generation and characterization of induced pluripotent stem (iPS) cell line (SDUCTi001-A) using fibroblasts derived from male-healthy donor. . 2022-12-00. Pubmed ID: 36402078; DOI: 10.1016/j.scr.2022.102961 SDUKIi002-ASDUCTi001-A 2022-12-00 2022-12-00 PubMed: 36402078 DOI: 10.1016/j.scr.2022.102961Associated cell lines:
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Fujii Yoichi Robertus
The MicroRNA 2000 Transformer
Fujii Yoichi Robertus. The MicroRNA 2000 Transformer. . 2023-00-00. DOI: 10.1007/978-981-99-3165-1 CSSi008-A 2023-00-00 2023-00-00 DOI: 10.1007/978-981-99-3165-1Associated cell lines:
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Huntemer-Silveira A, Malone D, Frie A, Walsh P, Parr AM
Accelerated differentiation of human induced pluripotent stem cells into regionally specific dorsal and ventral spinal neural progenitor cells for application in spinal cord therapeutics
Huntemer-Silveira A et al. Accelerated differentiation of human induced pluripotent stem cells into regionally specific dorsal and ventral spinal neural progenitor cells for application in spinal cord therapeutics. . 2023-00-00. Pubmed ID: 37781243; DOI: 10.3389/fnins.2023.1251906; PMC: PMC10540309 TMOi001-A 2023-00-00 2023-00-00 PubMed: 37781243 DOI: 10.3389/fnins.2023.1251906Associated cell lines:
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Stansfield BN, Rangasamy S, Ramsey K, Khanna M, Churko JM
Generation of an iPSC line from a Pontocerebellar Hypoplasia 1B patient harboring a homozygous c.395 A > C mutation in EXOSC3 along with a family matched control
Stansfield BN et al. Generation of an iPSC line from a Pontocerebellar Hypoplasia 1B patient harboring a homozygous c.395 A > C mutation in EXOSC3 along with a family matched control. . 2022-12-00. Pubmed ID: 36257093; DOI: 10.1016/j.scr.2022.102944; PMC: PMC9729447 UAZTi009-AUAZTi011-A 2022-12-00 2022-12-00 PubMed: 36257093 DOI: 10.1016/j.scr.2022.102944Associated cell lines:
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Yu S, Choi YJ, Rim JH, Kim HY, Bekheirnia N, Swartz SJ, Dai H, Gu SL, Lee S, Nishinakamura R, Hildebrandt F, Bekheirnia MR, Gee HY
Disease modeling of ADAMTS9-related nephropathy using kidney organoids reveals its roles in tubular cells and podocytes
Yu S et al. Disease modeling of ADAMTS9-related nephropathy using kidney organoids reveals its roles in tubular cells and podocytes. . 2023-00-00. Pubmed ID: 37035301; DOI: 10.3389/fmed.2023.1089159; PMC: PMC10079903 WISCi004-A 2023-00-00 2023-00-00 PubMed: 37035301 DOI: 10.3389/fmed.2023.1089159Associated cell lines:
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Bissoli I, D'Adamo S, Pignatti C, Agnetti G, Flamigni F, Cetrullo S
Induced pluripotent stem cell-based models: Are we ready for that heart in a dish?
Bissoli I et al. Induced pluripotent stem cell-based models: Are we ready for that heart in a dish?. . 2023-00-00. Pubmed ID: 36743420; DOI: 10.3389/fcell.2023.1129263; PMC: PMC9892938 MRIi028-AHMGUi003-A 2023-00-00 2023-00-00 PubMed: 36743420 DOI: 10.3389/fcell.2023.1129263Associated cell lines:
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Du JL, Gao LX, Wang T, Ye Z, Li HY, Li W, Zeng Q, Xi JF, Yue W, Li ZH
Influence of hypoxia on retinal progenitor and ganglion cells in human induced pluripotent stem cell-derived retinal organoids
Du JL et al. Influence of hypoxia on retinal progenitor and ganglion cells in human induced pluripotent stem cell-derived retinal organoids. . 2023-00-00. Pubmed ID: 37854379; DOI: 10.18240/ijo.2023.10.03; PMC: PMC10559029 FMCPGHi001-A 2023-00-00 2023-00-00 PubMed: 37854379 DOI: 10.18240/ijo.2023.10.03Associated cell lines:
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Chen IY, Olshausen J, Thomas D, Lai C, McLaughlin TL, Wu JC
Generation of three induced pluripotent stem cell lines to model and investigate diseases affecting Hispanics
Chen IY et al. Generation of three induced pluripotent stem cell lines to model and investigate diseases affecting Hispanics. . 2022-12-00. Pubmed ID: 36427473; DOI: 10.1016/j.scr.2022.102969; PMC: PMC10082602 SCVIi055-ASCVIi056-ASCVIi057-A 2022-12-00 2022-12-00 PubMed: 36427473 DOI: 10.1016/j.scr.2022.102969Associated cell lines:
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Li Q, Shao L, Li L, Shen H, Yu Y, Shen Z
Generation of a human embryonic stem cell line targeted homozygous deletion of BMP10 (WAe007-A-2) by CRISPR/Cas9-dgRNA
Li Q et al. Generation of a human embryonic stem cell line targeted homozygous deletion of BMP10 (WAe007-A-2) by CRISPR/Cas9-dgRNA. . 2022-12-00. Pubmed ID: 36257094; DOI: 10.1016/j.scr.2022.102942 WAe007-AWAe007-A-2 2022-12-00 2022-12-00 PubMed: 36257094 DOI: 10.1016/j.scr.2022.102942Associated cell lines:
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Shahriyari M, Islam MR, Sakib SM, Rinn M, Rika A, Krüger D, Kaurani L, Gisa V, Winterhoff M, Anandakumar H, Shomroni O, Schmidt M, Salinas G, Unger A, Linke WA, Zschüntzsch J, Schmidt J, Bassel-Duby R, Olson EN, Fischer A, Zimmermann WH, Tiburcy M
Engineered skeletal muscle recapitulates human muscle development, regeneration and dystrophy
Shahriyari M et al. Engineered skeletal muscle recapitulates human muscle development, regeneration and dystrophy. . 2022-12-00. Pubmed ID: 36254806; DOI: 10.1002/jcsm.13094; PMC: PMC9745484 RUCDRi002-A 2022-12-00 2022-12-00 PubMed: 36254806 DOI: 10.1002/jcsm.13094Associated cell lines:
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Supakul Sopak, Hatakeyama Yuki, Leventoux Nicolas, Itsuno Maika, Numata Naoko, Hiramine Hayato, Morimoto Satoru, Iwata Atsushi, Maeda Sumihiro, Okano Hideyuki
Urine-derived cells from the aged donor for the 2D/3D modeling of neural cells via iPSCs
Supakul Sopak et al. Urine-derived cells from the aged donor for the 2D/3D modeling of neural cells via iPSCs. . 2023-00-00. DOI: 10.1016/j.nbas.2023.100101 KEIOi005-A 2023-00-00 2023-00-00 DOI: 10.1016/j.nbas.2023.100101Associated cell lines:
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WANG YAFEI, NI JIELEI, LIU YUHAN, LIAO DINGYING, ZHOU QIANWEN, JI XIAOYANG, NIU GANG, NI YANXIANG
Realizing the potential of exploiting human IPSCs and their derivatives in research of Down syndrome
WANG YAFEI et al. Realizing the potential of exploiting human IPSCs and their derivatives in research of Down syndrome. . 2023-00-00. DOI: 10.32604/biocell.2023.043781 UUIGPi013-A 2023-00-00 2023-00-00 DOI: 10.32604/biocell.2023.043781Associated cell lines:
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Wang M, Tang J, Zhou T, Mai Y, Zhu Y
Generation of a homozygous FIS1 knockout human embryonic stem cell line GIBHe015-B by CRISPR/Cas9 system
Wang M et al. Generation of a homozygous FIS1 knockout human embryonic stem cell line GIBHe015-B by CRISPR/Cas9 system. . 2022-12-00. Pubmed ID: 36436397; DOI: 10.1016/j.scr.2022.102980 WAe001-A-1N 2022-12-00 2022-12-00 PubMed: 36436397 DOI: 10.1016/j.scr.2022.102980Associated cell lines:
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Yang D, Ling X, Liu F, Duan J, Bai F, Hu A
Generation of a human induced pluripotent stem cell line (SYSUTFi001-A) from infiltrating cytotoxic T cells in hepatocellular carcinoma (HCC)
Yang D et al. Generation of a human induced pluripotent stem cell line (SYSUTFi001-A) from infiltrating cytotoxic T cells in hepatocellular carcinoma (HCC). . 2022-12-00. Pubmed ID: 36375283; DOI: 10.1016/j.scr.2022.102962 SYSUTFi001-A 2022-12-00 2022-12-00 PubMed: 36375283 DOI: 10.1016/j.scr.2022.102962Associated cell lines:
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Leavens KF, Alvarez-Dominguez JR, Vo LT, Russ HA, Parent AV
Stem cell-based multi-tissue platforms to model human autoimmune diabetes
Leavens KF et al. Stem cell-based multi-tissue platforms to model human autoimmune diabetes. . 2022-12-00. Pubmed ID: 36209784; DOI: 10.1016/j.molmet.2022.101610; PMC: PMC9587366 SCSe001-ASCSe001-A-3 2022-12-00 2022-12-00 PubMed: 36209784 DOI: 10.1016/j.molmet.2022.101610Associated cell lines:
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Simorgh S, Mousavi SA, To SK, Pasque V, Wierda K, Vervliet T, Yeganeh M, Pooyan P, Chai YC, Verfaillie C, Baharvand H
A facile method to generate cerebral organoids from human pluripotent stem cells
Simorgh S et al. A facile method to generate cerebral organoids from human pluripotent stem cells. . 2023-00-00. Pubmed ID: 37927348; DOI: 10.17179/excli2023-6299; PMC: PMC10620858 SIGi001-A 2023-00-00 2023-00-00 PubMed: 37927348 DOI: 10.17179/excli2023-6299Associated cell lines:
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Kim JH, Hong JH, Kang KW, Lee BH, Park Y, Kim BS
Generation of the human pluripotent stem cell lines KUMi005-A from a patients with multiple myeloma
Kim JH et al. Generation of the human pluripotent stem cell lines KUMi005-A from a patients with multiple myeloma. . 2022-12-00. Pubmed ID: 36332466; DOI: 10.1016/j.scr.2022.102939 KUMi005-A 2022-12-00 2022-12-00 PubMed: 36332466 DOI: 10.1016/j.scr.2022.102939Associated cell lines:
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Abbott J, Tambe M, Pavlinov I, Farkhondeh A, Nguyen HN, Xu M, Pradhan M, York T, Might M, Baumgärtel K, Rodems S, Zheng W
Generation and characterization of NGLY1 patient-derived midbrain organoids
Abbott J et al. Generation and characterization of NGLY1 patient-derived midbrain organoids. . 2023-00-00. Pubmed ID: 36875753; DOI: 10.3389/fcell.2023.1039182; PMC: PMC9978932 TRNDi002-B 2023-00-00 2023-00-00 PubMed: 36875753 DOI: 10.3389/fcell.2023.1039182Associated cell lines:
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Lee J, Kim G, Chi KY, Han C, Kim JH
Generation of cytochrome P450 enzyme-polymorphic human induced pluripotent stem cell lines with CYP2D6*10/CYP3A5*3C and CYP2D6*10/CYP2C19*2
Lee J et al. Generation of cytochrome P450 enzyme-polymorphic human induced pluripotent stem cell lines with CYP2D6*10/CYP3A5*3C and CYP2D6*10/CYP2C19*2. . 2022-12-00. Pubmed ID: 36399926; DOI: 10.1016/j.scr.2022.102970 LSCTRi006-ALSCTRi007-A 2022-12-00 2022-12-00 PubMed: 36399926 DOI: 10.1016/j.scr.2022.102970Associated cell lines:
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Pongpaksupasin P, Wongkummool W, Tong-Ngam P, Jearawiriyapaisarn N, Paiboonsukwong K, Sangkitporn S, Trinavarat A, Atchaneeyasakul LO, Tubsuwan A
A generation of human-induced pluripotent stem cell line (MUi032-A) from a Choroideremia disease patient carrying a hemizygous mutation on the CHM gene
Pongpaksupasin P et al. A generation of human-induced pluripotent stem cell line (MUi032-A) from a Choroideremia disease patient carrying a hemizygous mutation on the CHM gene. . 2022-12-00. Pubmed ID: 36395688; DOI: 10.1016/j.scr.2022.102964 MUi031-AMUi032-A 2022-12-00 2022-12-00 PubMed: 36395688 DOI: 10.1016/j.scr.2022.102964 -
Sanz Francisco José, Solana-Manrique Cristina, Paricio Nuria
Modeling of Parkinson’s disease in Drosophila based on DJ-1 deficiency
Sanz Francisco José et al. Modeling of Parkinson’s disease in Drosophila based on DJ-1 deficiency. . 2023-00-00. DOI: 10.1016/b978-0-323-89833-1.00043-4 GIBHi004-A 2023-00-00 2023-00-00 DOI: 10.1016/b978-0-323-89833-1.00043-4Associated cell lines:
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Wu J, Tang Y
Transcription Factor-Mediated Differentiation of Motor Neurons from Human Pluripotent Stem Cells
Wu J et al. Transcription Factor-Mediated Differentiation of Motor Neurons from Human Pluripotent Stem Cells. . 2023-00-00. Pubmed ID: 36513936; DOI: 10.1007/978-1-0716-2811-9_16 CSUi002-A 2023-00-00 2023-00-00 PubMed: 36513936 DOI: 10.1007/978-1-0716-2811-9_16Associated cell lines:
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Arjmand Babak, Kokabi-Hamidpour Shayesteh, Aghayan Hamid Reza, Alavi-Moghadam Sepideh, Arjmand Rasta, Rezaei-Tavirani Mostafa, Goodarzi Parisa, Nasli-Esfahani Ensieh, Nikandish Mohsen
Stem Cell-Based Modeling Protocol for Parkinson’s Disease
Arjmand Babak et al. Stem Cell-Based Modeling Protocol for Parkinson’s Disease. . 2023-00-00. DOI: 10.1007/7651_2022_473 HEBHMUi001-A 2023-00-00 2023-00-00 DOI: 10.1007/7651_2022_473Associated cell lines:
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Follin Bjarke, Caluori Guido, Dobrolinska Magdalena M., Stachura Jarek, Muzzamil Hassan, Wojakowski Wojciech, Qayyum Abbas Ali, Jadczyk Tomasz
Induced Pluripotent Stem Cells and Allogeneic Mesenchymal Stem Cell Therapy in Cardiovascular Diseases
Follin Bjarke et al. Induced Pluripotent Stem Cells and Allogeneic Mesenchymal Stem Cell Therapy in Cardiovascular Diseases. . 2023-00-00. DOI: 10.1007/978-981-99-0722-9_3 EHTJUi004-A 2023-00-00 2023-00-00 DOI: 10.1007/978-981-99-0722-9_3Associated cell lines:
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Pierre M, Djemai M, Chapotte-Baldacci CA, Pouliot V, Puymirat J, Boutjdir M, Chahine M
Cardiac involvement in patient-specific induced pluripotent stem cells of myotonic dystrophy type 1: unveiling the impact of voltage-gated sodium channels
Pierre M et al. Cardiac involvement in patient-specific induced pluripotent stem cells of myotonic dystrophy type 1: unveiling the impact of voltage-gated sodium channels. . 2023-00-00. Pubmed ID: 37791351; DOI: 10.3389/fphys.2023.1258318; PMC: PMC10544896 CBRCULi001-ACBRCULi002-ACBRCULi003-ACBRCULi004-ACBRCULi005-A 2023-00-00 2023-00-00 PubMed: 37791351 DOI: 10.3389/fphys.2023.1258318Associated cell lines:
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Flores-Ponce X, López-Ornelas A, Escobedo-Avila I, Rodríguez-Violante M, Dávila-Ortiz de Montellano D, Cervantes-Arriaga A, Monroy-Jaramillo N, Velasco I
Generation of a human induced pluripotent stem cell line (UNAMi001-A) from a Mexican patient with sporadic Parkinson's disease
Flores-Ponce X et al. Generation of a human induced pluripotent stem cell line (UNAMi001-A) from a Mexican patient with sporadic Parkinson's disease. . 2022-12-00. Pubmed ID: 36427474; DOI: 10.1016/j.scr.2022.102972 UNAMi001-A 2022-12-00 2022-12-00 PubMed: 36427474 DOI: 10.1016/j.scr.2022.102972Associated cell lines:
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Tongbaen M, Matsumura Y, Okita K, Leecharoenkiat K
Generation of human induced pluripotent stem cells (CHULAi001-A) from peripheral blood mononuclear cells of a glucose-6-phosphate dehydrogenase (G6PD) deficient subject carrying the Viangchan mutation
Tongbaen M et al. Generation of human induced pluripotent stem cells (CHULAi001-A) from peripheral blood mononuclear cells of a glucose-6-phosphate dehydrogenase (G6PD) deficient subject carrying the Viangchan mutation. . 2022-12-00. Pubmed ID: 36334578; DOI: 10.1016/j.scr.2022.102953 CHULAi001-A 2022-12-00 2022-12-00 PubMed: 36334578 DOI: 10.1016/j.scr.2022.102953Associated cell lines:
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Schneider Y, Turan S, Koller A, Krumbiegel M, Farrell M, Plötz S, Winkler J, Xiang W
Generation of a homozygous and a heterozygous SNCA gene knockout human-induced pluripotent stem cell line by CRISPR/Cas9 mediated allele-specific tuning of SNCA expression
Schneider Y et al. Generation of a homozygous and a heterozygous SNCA gene knockout human-induced pluripotent stem cell line by CRISPR/Cas9 mediated allele-specific tuning of SNCA expression. . 2022-12-00. Pubmed ID: 36283273; DOI: 10.1016/j.scr.2022.102952 UKERi010-AUKERi010-A-1UKERi010-A-2 2022-12-00 2022-12-00 PubMed: 36283273 DOI: 10.1016/j.scr.2022.102952Associated cell lines:
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Holden Katie, Rath Phalguni, Drydale Edward, Bancroft James, Handunnetthi Lahiru
CRISPR/Cas9-mediated knockout of IL1RAPL1 in stem cells highlights a role in neural cell migration during cortical development
Holden Katie et al. CRISPR/Cas9-mediated knockout of IL1RAPL1 in stem cells highlights a role in neural cell migration during cortical development. . 2022-11-30. DOI: 10.21203/rs.3.rs-2326773/v1 WTSIi018-BWTSIi018-B-1 2022-11-30 2022-11-30 DOI: 10.21203/rs.3.rs-2326773/v1Associated cell lines:
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Su SA, Zhang Y, Li W, Xi Y, Lu Y, Shen J, Ma Y, Wang Y, Shen Y, Xie L, Ma H, Xie Y, Xiang M
Cardiac Piezo1 Exacerbates Lethal Ventricular Arrhythmogenesis by Linking Mechanical Stress with Ca(2+) Handling After Myocardial Infarction
Su SA et al. Cardiac Piezo1 Exacerbates Lethal Ventricular Arrhythmogenesis by Linking Mechanical Stress with Ca(2+) Handling After Myocardial Infarction. . 2023-00-00. Pubmed ID: 37303604; DOI: 10.34133/research.0165; PMC: PMC10255393 BCMi001-A 2023-00-00 2023-00-00 PubMed: 37303604 DOI: 10.34133/research.0165Associated cell lines:
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Jain N, Nagaich U, Pandey M, Chellappan DK, Dua K
Predictive genomic tools in disease stratification and targeted prevention: a recent update in personalized therapy advancements
Jain N et al. Predictive genomic tools in disease stratification and targeted prevention: a recent update in personalized therapy advancements. . 2022-12-00. Pubmed ID: 36505888; DOI: 10.1007/s13167-022-00304-2; PMC: PMC9727029 KSCBi015-A 2022-12-00 2022-12-00 PubMed: 36505888 DOI: 10.1007/s13167-022-00304-2Associated cell lines:
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Lv YF, Wang J, Cao CY, Zhang Y, Wang W
Production and characterization of human induced pluripotent stem cell line (PUMCi002-A) from a Krabbe patient related control to study disease mechanisms associated with GALC mutation
Lv YF et al. Production and characterization of human induced pluripotent stem cell line (PUMCi002-A) from a Krabbe patient related control to study disease mechanisms associated with GALC mutation. . 2022-12-00. Pubmed ID: 36270068; DOI: 10.1016/j.scr.2022.102945 PUMCi001-APUMCi002-A 2022-12-00 2022-12-00 PubMed: 36270068 DOI: 10.1016/j.scr.2022.102945Associated cell lines:
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Wongkummool W, Tong-Ngam P, Munkongdee T, Tangprasittipap A, Paiboonsukwong K, Hongeng S, Fucharoen S, Charoenkwan P, Tubsuwan A
Generation of human induced pluripotent stem cell line (MUi034-A) from an unusual case of hydrops fetalis associated with homozygous hemoglobin Constant Spring
Wongkummool W et al. Generation of human induced pluripotent stem cell line (MUi034-A) from an unusual case of hydrops fetalis associated with homozygous hemoglobin Constant Spring. . 2022-12-00. Pubmed ID: 36427475; DOI: 10.1016/j.scr.2022.102979 MUi031-AMUi034-A 2022-12-00 2022-12-00 PubMed: 36427475 DOI: 10.1016/j.scr.2022.102979 -
Maghazachi AA
Globoid Cell Leukodystrophy (Krabbe Disease): An Update
Maghazachi AA. Globoid Cell Leukodystrophy (Krabbe Disease): An Update. . 2023-00-00. Pubmed ID: 37928748; DOI: 10.2147/itt.s424622; PMC: PMC10625317 PUMCi002-A 2023-00-00 2023-00-00 PubMed: 37928748 DOI: 10.2147/itt.s424622Associated cell lines:
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Puri D, Maaßen C, Varona Baranda M, Zeevaert K, Hahnfeld L, Hauser A, Fornero G, Elsafi Mabrouk MH, Wagner W
CTCF deletion alters the pluripotency and DNA methylation profile of human iPSCs
Puri D et al. CTCF deletion alters the pluripotency and DNA methylation profile of human iPSCs. . 2023-00-00. Pubmed ID: 38099298; DOI: 10.3389/fcell.2023.1302448; PMC: PMC10720430 UKAi009-AUKAi010-AUKAi011-A 2023-00-00 2023-00-00 PubMed: 38099298 DOI: 10.3389/fcell.2023.1302448 -
Febbraro F, Andersen HHB, Kitt MM, Willnow TE
Spatially and temporally distinct patterns of expression for VPS10P domain receptors in human cerebral organoids
Febbraro F et al. Spatially and temporally distinct patterns of expression for VPS10P domain receptors in human cerebral organoids. . 2023-00-00. Pubmed ID: 37842085; DOI: 10.3389/fcell.2023.1229584; PMC: PMC10570844 HMGUi001-A 2023-00-00 2023-00-00 PubMed: 37842085 DOI: 10.3389/fcell.2023.1229584Associated cell lines:
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Gao K, Lin Z, Wen S, Jiang Y
Potassium channels and epilepsy
Gao K et al. Potassium channels and epilepsy. . 2022-12-00. Pubmed ID: 36225112; DOI: 10.1111/ane.13695 GZHMCi001-AGZHMCi001-BZJSHi001-ASHCDNi006-A 2022-12-00 2022-12-00 PubMed: 36225112 DOI: 10.1111/ane.13695Associated cell lines:
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Li S, Liu H, Liu W, Shi N, Zhao M, Wanggou S, Luo W, Wang L, Zhu B, Zuo X, Xie W, Zhao C, Zhou Y, Luo L, Gao X, Jiang X, Ren C
ESRG is critical to maintain the cell survival and self-renewal/pluripotency of hPSCs by collaborating with MCM2 to suppress p53 pathway
Li S et al. ESRG is critical to maintain the cell survival and self-renewal/pluripotency of hPSCs by collaborating with MCM2 to suppress p53 pathway. . 2023-00-00. Pubmed ID: 36778110; DOI: 10.7150/ijbs.79095; PMC: PMC9909993 CSUe011-A 2023-00-00 2023-00-00 PubMed: 36778110 DOI: 10.7150/ijbs.79095Associated cell lines:
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Lin H, Ye SQ, Xu ZH, Penaloza JS, Aljuhani M, Vetter T, Zhao MT, McBride KL
Generation and characterization of a human induced pluripotent stem cell (iPSC) line from a patient with congenital heart disease (CHD)
Lin H et al. Generation and characterization of a human induced pluripotent stem cell (iPSC) line from a patient with congenital heart disease (CHD). . 2022-12-00. Pubmed ID: 36343514; DOI: 10.1016/j.scr.2022.102958; PMC: PMC9831069 CHUQi001-ANCHi001-A 2022-12-00 2022-12-00 PubMed: 36343514 DOI: 10.1016/j.scr.2022.102958Associated cell lines:
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Hao Ruochen, Wang Qinglin, Yin Shangfei, Zhou Tianyang, Zhang Qingyang, Mei Songzhu, Shen Siqi, Liu Jie
Optimizing Depthwise Convolutions on ARMv8 Architecture
Hao Ruochen et al. Optimizing Depthwise Convolutions on ARMv8 Architecture. . 2023-00-00. DOI: 10.1007/978-3-031-29927-8_34 ZZUNEUi017-A 2023-00-00 2023-00-00 DOI: 10.1007/978-3-031-29927-8_34Associated cell lines:
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Lee N, Moon HJ, Park SH, Moon JY, Park KK, Kim JH, Lee JH
Generation of Parkinson's disease patient-derived human induced pluripotent stem cells line (PNUSCRi001-A) carrying a N227S mutation in GBA gene
Lee N et al. Generation of Parkinson's disease patient-derived human induced pluripotent stem cells line (PNUSCRi001-A) carrying a N227S mutation in GBA gene. . 2022-12-00. Pubmed ID: 36332465; DOI: 10.1016/j.scr.2022.102959 PNUSCRi001-A 2022-12-00 2022-12-00 PubMed: 36332465 DOI: 10.1016/j.scr.2022.102959Associated cell lines:
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Chimata P, Kashyap DK, Sairam T, Ganesh A, Thangaraj K, Purushottam M, Viswanath B, Jain S, Dhandapany PS
Generation of a new human induced pluripotent stem cell (hiPSC) line from a South Asian Indian with a MYBPC3(Δ)(25bp) variant
Chimata P et al. Generation of a new human induced pluripotent stem cell (hiPSC) line from a South Asian Indian with a MYBPC3(Δ)(25bp) variant. . 2022-12-00. Pubmed ID: 36403549; DOI: 10.1016/j.scr.2022.102978 CBDTi001-A 2022-12-00 2022-12-00 PubMed: 36403549 DOI: 10.1016/j.scr.2022.102978Associated cell lines:
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Stolzenburg LR, Esmaeeli S, Kulkarni AS, Murphy E, Kwon T, Preiss C, Bahnassawy L, Stender JD, Manos JD, Reinhardt P, Rahimov F, Waring JF, Ramathal CY
Functional characterization of a single nucleotide polymorphism associated with Alzheimer's disease in a hiPSC-based neuron model
Stolzenburg LR et al. Functional characterization of a single nucleotide polymorphism associated with Alzheimer's disease in a hiPSC-based neuron model. . 2023-00-00. Pubmed ID: 37751459; DOI: 10.1371/journal.pone.0291029; PMC: PMC10521995 BIONi010-CBIONi010-C-13 2023-00-00 2023-00-00 PubMed: 37751459 DOI: 10.1371/journal.pone.0291029Associated cell lines:
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Zhang TT, Zhao SR, Alamana C, Shen M, Parikh V, Wheeler MT, Wu JC
Generation of two induced pluripotent stem cell lines from dilated cardiomyopathy patients carrying TTN mutations
Zhang TT et al. Generation of two induced pluripotent stem cell lines from dilated cardiomyopathy patients carrying TTN mutations. . 2022-12-00. Pubmed ID: 36270069; DOI: 10.1016/j.scr.2022.102941; PMC: PMC9870071 SCVIi046-ASCVIi068-A 2022-12-00 2022-12-00 PubMed: 36270069 DOI: 10.1016/j.scr.2022.102941Associated cell lines:
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Cota P, Saber L, Taskin D, Jing C, Bastidas-Ponce A, Vanheusden M, Shahryari A, Sterr M, Burtscher I, Bakhti M, Lickert H
NEUROD2 function is dispensable for human pancreatic β cell specification
Cota P et al. NEUROD2 function is dispensable for human pancreatic β cell specification. . 2023-00-00. Pubmed ID: 37955006; DOI: 10.3389/fendo.2023.1286590; PMC: PMC10634430 HMGUi001-AHMGUi001-A-8HMGUi001-A-42 2023-00-00 2023-00-00 PubMed: 37955006 DOI: 10.3389/fendo.2023.1286590Associated cell lines:
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Huang P, Tian C, Chen Y, Zhou M, Ni J, Niu M, Liu X, Peng Z
Generation of a NIS-EGFP-Fluc triple-reporter human embryonic stem cell line by PiggyBac transposon system
Huang P et al. Generation of a NIS-EGFP-Fluc triple-reporter human embryonic stem cell line by PiggyBac transposon system. . 2022-12-00. Pubmed ID: 36403548; DOI: 10.1016/j.scr.2022.102968 WAe009-A-93 2022-12-00 2022-12-00 PubMed: 36403548 DOI: 10.1016/j.scr.2022.102968Associated cell lines:
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Yildirim Z, Kojic A, Yan CD, Wu MA, Vagelos R, Wu JC
Generation of two induced pluripotent stem cell lines from dilated cardiomyopathy patients caused by heterozygous mutations in the HCN4 gene
Yildirim Z et al. Generation of two induced pluripotent stem cell lines from dilated cardiomyopathy patients caused by heterozygous mutations in the HCN4 gene. . 2022-12-00. Pubmed ID: 36332467; DOI: 10.1016/j.scr.2022.102951; PMC: PMC9881502 SCVIi063-ASCVIi064-A 2022-12-00 2022-12-00 PubMed: 36332467 DOI: 10.1016/j.scr.2022.102951Associated cell lines:
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Chan AP, Choi Y, Rangan A, Zhang G, Podder A, Berens M, Sharma S, Pirrotte P, Byron S, Duggan D, Schork NJ
Interrogating the Human Diplome: Computational Methods, Emerging Applications, and Challenges
Chan AP et al. Interrogating the Human Diplome: Computational Methods, Emerging Applications, and Challenges. . 2023-00-00. Pubmed ID: 36335489; DOI: 10.1007/978-1-0716-2819-5_1 BIONi010-C 2023-00-00 2023-00-00 PubMed: 36335489 DOI: 10.1007/978-1-0716-2819-5_1Associated cell lines:
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Kwon OS, Na HJ, Ahn J, Chung KS
Establishment of a human induced pluripotent stem cell line, KRIBBi006-A, from peripheral blood mononuclear cells derived from a healthy male donor
Kwon OS et al. Establishment of a human induced pluripotent stem cell line, KRIBBi006-A, from peripheral blood mononuclear cells derived from a healthy male donor. . 2022-12-00. Pubmed ID: 36283271; DOI: 10.1016/j.scr.2022.102950 KRIBBi006-A 2022-12-00 2022-12-00 PubMed: 36283271 DOI: 10.1016/j.scr.2022.102950Associated cell lines:
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Zhou Y, Jiang C, Wang J, Huang W, Zhang Y, Zhou R
Generation of one human induced pluripotent stem cell line (XACHi004-A) with heterozygous mutation of RYR2 gene from an atrial fibrillation patient
Zhou Y et al. Generation of one human induced pluripotent stem cell line (XACHi004-A) with heterozygous mutation of RYR2 gene from an atrial fibrillation patient. . 2022-12-00. Pubmed ID: 36335801; DOI: 10.1016/j.scr.2022.102955 XACHi004-AXACHi005-AXACHi006-ASDQLCHi032-A 2022-12-00 2022-12-00 PubMed: 36335801 DOI: 10.1016/j.scr.2022.102955Associated cell lines:
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Valente O, Dobner J, Ramachandran H, Hildebrandt B, Distelmaier F, Ventura N, Rossi A
Generation of an induced pluripotent stem cell line (IUFi002-A) from a Leigh syndrome patient carrying mutations in the NDUFS1 gene
Valente O et al. Generation of an induced pluripotent stem cell line (IUFi002-A) from a Leigh syndrome patient carrying mutations in the NDUFS1 gene. . 2022-12-00. Pubmed ID: 36403546; DOI: 10.1016/j.scr.2022.102971 IUFi002-A 2022-12-00 2022-12-00 PubMed: 36403546 DOI: 10.1016/j.scr.2022.102971Associated cell lines:
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Cao Y, Tian W, Cao L, Lv W, Zheng L, Luan X
Generation of an induced pluripotent stem cell JTUi005-A from a patient with neuronal intranuclear inclusion disease
Cao Y et al. Generation of an induced pluripotent stem cell JTUi005-A from a patient with neuronal intranuclear inclusion disease. . 2022-12-00. Pubmed ID: 36244083; DOI: 10.1016/j.scr.2022.102938 JTUi005-A 2022-12-00 2022-12-00 PubMed: 36244083 DOI: 10.1016/j.scr.2022.102938Associated cell lines:
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López-Ramírez O, González-Garrido A
The role of acid sensing ion channels in the cardiovascular function
López-Ramírez O et al. The role of acid sensing ion channels in the cardiovascular function. . 2023-00-00. Pubmed ID: 37389121; DOI: 10.3389/fphys.2023.1194948; PMC: PMC10300344 UKKi011-A 2023-00-00 2023-00-00 PubMed: 37389121 DOI: 10.3389/fphys.2023.1194948Associated cell lines:
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Kim SH, Ku YA, Yoo C, Kim YH, Kim DH
Comparison of RCI001 and corticosteroid on the effects on intraocular pressure in mice
Kim SH et al. Comparison of RCI001 and corticosteroid on the effects on intraocular pressure in mice. . 2023-00-00. Pubmed ID: 37877019; DOI: 10.3389/fmed.2023.1256569; PMC: PMC10591319 RCi001-A 2023-00-00 2023-00-00 PubMed: 37877019 DOI: 10.3389/fmed.2023.1256569Associated cell lines:
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Giallongo S, Lo Re O, Resnick I, Raffaele M, Vinciguerra M
Gene Editing and Human iPSCs in Cardiovascular and Metabolic Diseases
Giallongo S et al. Gene Editing and Human iPSCs in Cardiovascular and Metabolic Diseases. . 2023-00-00. Pubmed ID: 36454473; DOI: 10.1007/978-981-19-5642-3_18 UAMi004-A-1 2023-00-00 2023-00-00 PubMed: 36454473 DOI: 10.1007/978-981-19-5642-3_18Associated cell lines:
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Ali G, Habbab W, Alkhadairi G, Al-Shaban FA, Stanton LW
Generation of induced pluripotent stem cell lines from nonaffected parents and monozygotic triplets affected with autism spectrum disorder and epilepsy
Ali G et al. Generation of induced pluripotent stem cell lines from nonaffected parents and monozygotic triplets affected with autism spectrum disorder and epilepsy. . 2022-12-00. Pubmed ID: 36272305; DOI: 10.1016/j.scr.2022.102943 QBRIi014-AQBRIi015-AQBRIi016-AQBRIi017-AQBRIi018-A 2022-12-00 2022-12-00 PubMed: 36272305 DOI: 10.1016/j.scr.2022.102943Associated cell lines:
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Sam Im Y, Hoon Yoo D, Kim HE, Young Oh J, Kim YO
Generation of integration-free induced pluripotent stem cell line (KSCBi017-A) from peripheral blood mononuclear cells of a healthy male individual
Sam Im Y et al. Generation of integration-free induced pluripotent stem cell line (KSCBi017-A) from peripheral blood mononuclear cells of a healthy male individual. . 2022-12-00. Pubmed ID: 36403547; DOI: 10.1016/j.scr.2022.102965 KSCBi017-A 2022-12-00 2022-12-00 PubMed: 36403547 DOI: 10.1016/j.scr.2022.102965Associated cell lines:
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Tang LV, Tao Y, Feng Y, Ma J, Lin W, Zhang Y, Zhang Y, Wu T, Cai Y, Lu H, Wei J, Corral J, Hu Y
Gene editing of human iPSCs rescues thrombophilia in hereditary antithrombin deficiency in mice
Tang LV et al. Gene editing of human iPSCs rescues thrombophilia in hereditary antithrombin deficiency in mice. . 2022-11-30. Pubmed ID: 36449603; DOI: 10.1126/scitranslmed.abq3202 ZZUNEUi014-A 2022-11-30 2022-11-30 PubMed: 36449603 DOI: 10.1126/scitranslmed.abq3202Associated cell lines:
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Willumsen N, Arber C, Lovejoy C, Toombs J, Alatza A, Weston PSJ, Chávez-Gutiérrez L, Hardy J, Zetterberg H, Fox NC, Ryan NS, Lashley T, Wray S
The PSEN1 E280G mutation leads to increased amyloid-β43 production in induced pluripotent stem cell neurons and deposition in brain tissue
Willumsen N et al. The PSEN1 E280G mutation leads to increased amyloid-β43 production in induced pluripotent stem cell neurons and deposition in brain tissue. . 2023-00-00. Pubmed ID: 36687397; DOI: 10.1093/braincomms/fcac321; PMC: PMC9847549 RBi001-ASIGi001-ASIGi001-A-1 2023-00-00 2023-00-00 PubMed: 36687397 DOI: 10.1093/braincomms/fcac321Associated cell lines:
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Noh KM, Park SJ, Moon SH, Jung SY
Extracellular matrix cues regulate the differentiation of pluripotent stem cell-derived endothelial cells
Noh KM et al. Extracellular matrix cues regulate the differentiation of pluripotent stem cell-derived endothelial cells. . 2023-00-00. Pubmed ID: 37435057; DOI: 10.3389/fcvm.2023.1169331; PMC: PMC10330705 WISCi004-ABCRTi005-ABIHi004-A 2023-00-00 2023-00-00 PubMed: 37435057 DOI: 10.3389/fcvm.2023.1169331Associated cell lines:
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Ronima K R, Dey Chandrima, Thummer Rajkumar P.
An Insight into the Role of GLIS1 in Embryonic Development, iPSC Generation, and Cancer
Ronima K R et al. An Insight into the Role of GLIS1 in Embryonic Development, iPSC Generation, and Cancer. . 2023-00-00. DOI: 10.1007/5584_2023_793 RCMGi002-ARCMGi004-A 2023-00-00 2023-00-00 DOI: 10.1007/5584_2023_793Associated cell lines:
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Gasser J, Gillet G, Valadas JS, Rouvière L, Kotian A, Fan W, Keaney J, Kadiu I
Innate immune activation and aberrant function in the R6/2 mouse model and Huntington's disease iPSC-derived microglia
Gasser J et al. Innate immune activation and aberrant function in the R6/2 mouse model and Huntington's disease iPSC-derived microglia. . 2023-00-00. Pubmed ID: 37415834; DOI: 10.3389/fnmol.2023.1191324; PMC: PMC10319581 RCi004-A 2023-00-00 2023-00-00 PubMed: 37415834 DOI: 10.3389/fnmol.2023.1191324Associated cell lines:
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Dorschel KB, Wanebo JE
Physiological and pathophysiological mechanisms of the molecular and cellular biology of angiogenesis and inflammation in moyamoya angiopathy and related vascular diseases
Dorschel KB et al. Physiological and pathophysiological mechanisms of the molecular and cellular biology of angiogenesis and inflammation in moyamoya angiopathy and related vascular diseases. . 2023-00-00. Pubmed ID: 37273690; DOI: 10.3389/fneur.2023.661611; PMC: PMC10236939 HUSTTJi001-A 2023-00-00 2023-00-00 PubMed: 37273690 DOI: 10.3389/fneur.2023.661611Associated cell lines:
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Abdolkarimi D, Cunha DL, Lahne M, Moosajee M
PAX6 disease models for aniridia
Abdolkarimi D et al. PAX6 disease models for aniridia. . 2022-12-00. Pubmed ID: 36453299; DOI: 10.4103/ijo.ijo_316_22; PMC: PMC9940591 SDQLCHi010-AUCLi013-A 2022-12-00 2022-12-00 PubMed: 36453299 DOI: 10.4103/ijo.ijo_316_22Associated cell lines:
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Catania M, Colombo L, Sorrentino S, Cagnotto A, Lucchetti J, Barbagallo MC, Vannetiello I, Vecchi ER, Favagrossa M, Costanza M, Giaccone G, Salmona M, Tagliavini F, Di Fede G
A novel bio-inspired strategy to prevent amyloidogenesis and synaptic damage in Alzheimer's disease
Catania M et al. A novel bio-inspired strategy to prevent amyloidogenesis and synaptic damage in Alzheimer's disease. . 2022-12-00. Pubmed ID: 36028569; DOI: 10.1038/s41380-022-01745-x; PMC: PMC9763104 UEFi003-A 2022-12-00 2022-12-00 PubMed: 36028569 DOI: 10.1038/s41380-022-01745-xAssociated cell lines:
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Maurizi A
Experimental therapies for osteopetrosis
Maurizi A. Experimental therapies for osteopetrosis. . 2022-12-00. Pubmed ID: 36152941; DOI: 10.1016/j.bone.2022.116567 BIHi002-A 2022-12-00 2022-12-00 PubMed: 36152941 DOI: 10.1016/j.bone.2022.116567Associated cell lines:
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Zhou Qingjun, Li Zongyi, Duan Haoyun
iPSC-Derived Corneal Endothelial Cells
Zhou Qingjun et al. iPSC-Derived Corneal Endothelial Cells. . 2023-00-00. DOI: 10.1007/164_2023_644 KAIMRCi001-A 2023-00-00 2023-00-00 DOI: 10.1007/164_2023_644Associated cell lines:
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Mun D, Kang JY, Chun Y, Park DS, Kim H, Yun N, Lee SH, Joung B
Generation of two PITX2 knock-out human induced pluripotent stem cell lines using CRISPR/Cas9 system
Mun D et al. Generation of two PITX2 knock-out human induced pluripotent stem cell lines using CRISPR/Cas9 system. . 2022-12-00. Pubmed ID: 36260954; DOI: 10.1016/j.scr.2022.102940 KSCBi018-A-6KSCBi018-A-7 2022-12-00 2022-12-00 PubMed: 36260954 DOI: 10.1016/j.scr.2022.102940Associated cell lines:
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Maria Turco E, Maria Giada Giovenale A, Rotundo G, Mazzoni M, Zanfardino P, Frezza K, Torrente I, Mary Carletti R, Damiani D, Santorelli FM, Luigi Vescovi A, Petruzzella V, Rosati J
Generation and characterization of CSSi016-A (9938) human pluripotent stem cell line carrying two biallelic variants in MTMR5/SBF1 gene resulting in a case of severe CMT4B3
Maria Turco E et al. Generation and characterization of CSSi016-A (9938) human pluripotent stem cell line carrying two biallelic variants in MTMR5/SBF1 gene resulting in a case of severe CMT4B3. . 2022-12-00. Pubmed ID: 36272304; DOI: 10.1016/j.scr.2022.102946 CSSi016-A 2022-12-00 2022-12-00 PubMed: 36272304 DOI: 10.1016/j.scr.2022.102946Associated cell lines:
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Cumberland MJ, Euchner J, Azad AJ, T N Vo N, Kirchhof P, Holmes AP, Denning C, Gehmlich K
Generation of a human iPSC-derived cardiomyocyte/fibroblast engineered heart tissue model
Cumberland MJ et al. Generation of a human iPSC-derived cardiomyocyte/fibroblast engineered heart tissue model. . 2023-00-00. Pubmed ID: 38298530; DOI: 10.12688/f1000research.139482.1; PMC: PMC10828555 WTSIi018-AWTSIi018-B 2023-00-00 2023-00-00 PubMed: 38298530 DOI: 10.12688/f1000research.139482.1Associated cell lines:
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Mehta A, Yu Q, Liu Y, Yang D, Zou J, Beers J, de Jesus Rasheed AA, Rastegar AT, Goldbach-Mansky R, Boehm M, Chen G
Human induced pluripotent stem cells generated from STING-associated vasculopathy with onset in infancy (SAVI) patients with a heterozygous mutation in the STING gene
Mehta A et al. Human induced pluripotent stem cells generated from STING-associated vasculopathy with onset in infancy (SAVI) patients with a heterozygous mutation in the STING gene. . 2022-12-00. Pubmed ID: 36399927; DOI: 10.1016/j.scr.2022.102974; PMC: PMC9799028 NIHTVBi024-ANIHTVBi025-ANIHTVBi026-ANIHTVBi027-A 2022-12-00 2022-12-00 PubMed: 36399927 DOI: 10.1016/j.scr.2022.102974Associated cell lines:
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Zhou Guangqian
Application potentials of the iPSC technology in modeling, drug discovery and regeneration of skeletal system disorders
Zhou Guangqian. Application potentials of the iPSC technology in modeling, drug discovery and regeneration of skeletal system disorders. . 2023-00-00. DOI: 10.1016/b978-0-323-91938-8.00010-x ISMMSi002-B 2023-00-00 2023-00-00 DOI: 10.1016/b978-0-323-91938-8.00010-xAssociated cell lines:
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Moon HJ, Lee N, Moon JY, Park KK, Lee JH, Kim JH
Human induced pluripotent stem cells line (PNUSCRi002-A) from a patient with Parkinson's disease carrying a R159W mutation in the GBA gene
Moon HJ et al. Human induced pluripotent stem cells line (PNUSCRi002-A) from a patient with Parkinson's disease carrying a R159W mutation in the GBA gene. . 2022-12-00. Pubmed ID: 36274270; DOI: 10.1016/j.scr.2022.102948 PNUSCRi002-A 2022-12-00 2022-12-00 PubMed: 36274270 DOI: 10.1016/j.scr.2022.102948Associated cell lines:
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Lee CH, Hunt D, Roth JG, Chiu CC, Suhar RA, LeSavage BL, Seymour AJ, Lindsay C, Krajina BA, Chen YT, Chang KH, Hsieh IC, Chu PH, Wen MS, Heilshorn SC
Tuning pro-survival effects of human induced pluripotent stem cell-derived exosomes using elastin-like polypeptides
Lee CH et al. Tuning pro-survival effects of human induced pluripotent stem cell-derived exosomes using elastin-like polypeptides. . 2022-12-00. Pubmed ID: 36343608; DOI: 10.1016/j.biomaterials.2022.121864 DHMCi005-A 2022-12-00 2022-12-00 PubMed: 36343608 DOI: 10.1016/j.biomaterials.2022.121864Associated cell lines:
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Ding T, Zhu W, Li X, Jian L
Reprogramming of a human induced pluripotent stem cell line (ZZUSAHi004-A) from a long QT syndrome patient with a heterozygous AKAP9 (c. 4021C > A) mutant
Ding T et al. Reprogramming of a human induced pluripotent stem cell line (ZZUSAHi004-A) from a long QT syndrome patient with a heterozygous AKAP9 (c. 4021C > A) mutant. . 2022-12-00. Pubmed ID: 36395689; DOI: 10.1016/j.scr.2022.102966 ZZUSAHi004-A 2022-12-00 2022-12-00 PubMed: 36395689 DOI: 10.1016/j.scr.2022.102966Associated cell lines:
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Tucker A, Dulin JN
The Emerging Role of Biological Sex in Cell Therapy for Spinal Cord Injury
Tucker A et al. The Emerging Role of Biological Sex in Cell Therapy for Spinal Cord Injury. . 2023-00-00. Pubmed ID: 36798608; DOI: 10.1177/26331055231153128; PMC: PMC9925999 WAe009-A 2023-00-00 2023-00-00 PubMed: 36798608 DOI: 10.1177/26331055231153128Associated cell lines:
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Dicks AR, Steward N, Guilak F, Wu CL
Chondrogenic Differentiation of Human-Induced Pluripotent Stem Cells
Dicks AR et al. Chondrogenic Differentiation of Human-Induced Pluripotent Stem Cells. . 2023-00-00. Pubmed ID: 36355287; DOI: 10.1007/978-1-0716-2839-3_8; PMC: PMC9830630 MCRIi001-AMCRIi001-A-3MCRIi001-A-4 2023-00-00 2023-00-00 PubMed: 36355287 DOI: 10.1007/978-1-0716-2839-3_8Associated cell lines:
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Boudesco C, Nonneman A, Cinti A, Picardi P, Redaelli L, Swijsen S, Roewe J, Reinhardt P, Ibach M, Walter J, Pocock JM, Ren Y, Driguez PA, Dargazanli G, Eyquem S, Proto J, Flores-Morales A, Pradier L
Novel potent liposome agonists of triggering receptor expressed on myeloid cells 2 phenocopy antibody treatment in cells
Boudesco C et al. Novel potent liposome agonists of triggering receptor expressed on myeloid cells 2 phenocopy antibody treatment in cells. . 2022-12-00. Pubmed ID: 35912412; DOI: 10.1002/glia.24252; PMC: PMC9804933 BIONi010-CBIONi010-C-17 2022-12-00 2022-12-00 PubMed: 35912412 DOI: 10.1002/glia.24252Associated cell lines:
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Su PY, Lee W, Zernant J, Tsang SH, Nagasaki T, Corneo B, Allikmets R
Establishment of the iPSC line CUIMCi005-A from a patient with Stargardt disease for retinal organoid culture
Su PY et al. Establishment of the iPSC line CUIMCi005-A from a patient with Stargardt disease for retinal organoid culture. . 2022-12-00. Pubmed ID: 36455383; DOI: 10.1016/j.scr.2022.102973; PMC: PMC9801682 CUIMCi005-A 2022-12-00 2022-12-00 PubMed: 36455383 DOI: 10.1016/j.scr.2022.102973Associated cell lines:
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Perik M, Verstraeten A, Nijak-Paeske A, Rabaut L, Van Laer L, Loeys B
Generation of a human TGFB3-hIPSC line, BBANTWi010-A, from a Loeys-Dietz syndrome type V patient
Perik M et al. Generation of a human TGFB3-hIPSC line, BBANTWi010-A, from a Loeys-Dietz syndrome type V patient. . 2022-12-00. Pubmed ID: 36356561; DOI: 10.1016/j.scr.2022.102956 BBANTWi010-A 2022-12-00 2022-12-00 PubMed: 36356561 DOI: 10.1016/j.scr.2022.102956Associated cell lines:
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Baliña-Sánchez C, Aguilera Y, Adán N, Sierra-Párraga JM, Olmedo-Moreno L, Panadero-Morón C, Cabello-Laureano R, Márquez-Vega C, Martín-Montalvo A, Capilla-González V
Generation of mesenchymal stromal cells from urine-derived iPSCs of pediatric brain tumor patients
Baliña-Sánchez C et al. Generation of mesenchymal stromal cells from urine-derived iPSCs of pediatric brain tumor patients. . 2023-00-00. Pubmed ID: 36776860; DOI: 10.3389/fimmu.2023.1022676; PMC: PMC9910217 ZJUCHi001-ASDQLCHi014-AWMUi021-AESi087-AESi088-AESi089-AESi090-A 2023-00-00 2023-00-00 PubMed: 36776860 DOI: 10.3389/fimmu.2023.1022676Associated cell lines:
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Miller DC, Lisowski P, Lickfett S, Mlody B, Bünning M, Genehr C, Ulrich C, Wanker EE, Diecke S, Priller J, Prigione A
Generation of induced pluripotent stem cells from three individuals with Huntington's disease
Miller DC et al. Generation of induced pluripotent stem cells from three individuals with Huntington's disease. . 2022-12-00. Pubmed ID: 36434993; DOI: 10.1016/j.scr.2022.102976 BIHi033-ABIHi034-ABIHi288-A 2022-12-00 2022-12-00 PubMed: 36434993 DOI: 10.1016/j.scr.2022.102976 -
Zhang L, Liu X, Huang M, Xu P, Lai Y, Liu Y, Zhong X, Li S, Ding X
Generation of a X-linked juvenile retinoschisis patient-derived induced pluripotent stem cell line ZOCi004-A
Zhang L et al. Generation of a X-linked juvenile retinoschisis patient-derived induced pluripotent stem cell line ZOCi004-A. . 2022-12-00. Pubmed ID: 36270067; DOI: 10.1016/j.scr.2022.102937 ZOCi004-A 2022-12-00 2022-12-00 PubMed: 36270067 DOI: 10.1016/j.scr.2022.102937Associated cell lines:
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Rui Q, Tan J, Jin J, Ye W, Zhou Y, Chen J
Establishment of a PBMC-derived induced pluripotent stem cell (NJUCMi001-A) from a patient with LAMA2-related congenital muscular dystrophy (MDC1A) carrying frameshift deletion c.3367delA in LAMA2 gene
Rui Q et al. Establishment of a PBMC-derived induced pluripotent stem cell (NJUCMi001-A) from a patient with LAMA2-related congenital muscular dystrophy (MDC1A) carrying frameshift deletion c.3367delA in LAMA2 gene. . 2022-12-00. Pubmed ID: 36334577; DOI: 10.1016/j.scr.2022.102957 NJUCMi001-A 2022-12-00 2022-12-00 PubMed: 36334577 DOI: 10.1016/j.scr.2022.102957Associated cell lines:
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Luconi M, Sogorb M, Markert U, Benfenati E, May T, Wolbank S, Roncaglioni A, Schmidt A, Straccia M, Tait S.
Human-Based New Approach Methodologies in Developmental Toxicity Testing: A Step Ahead from the State of the Art with a Feto–Placental Organ-on-Chip Platform
Luconi M et al. Human-Based New Approach Methodologies in Developmental Toxicity Testing: A Step Ahead from the State of the Art with a Feto–Placental Organ-on-Chip Platform. . 2022-11-28. BIONi010-C 2022-11-28 2022-11-28Associated cell lines:
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Luconi M, Sogorb MA, Markert UR, Benfenati E, May T, Wolbank S, Roncaglioni A, Schmidt A, Straccia M, Tait S
Human-Based New Approach Methodologies in Developmental Toxicity Testing: A Step Ahead from the State of the Art with a Feto-Placental Organ-on-Chip Platform
Luconi M et al. Human-Based New Approach Methodologies in Developmental Toxicity Testing: A Step Ahead from the State of the Art with a Feto-Placental Organ-on-Chip Platform. . 2022-11-28. Pubmed ID: 36497907; DOI: 10.3390/ijerph192315828; PMC: PMC9737555 BIONi010-C 2022-11-28 2022-11-28 PubMed: 36497907 DOI: 10.3390/ijerph192315828Associated cell lines:
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Damkham N, Issaragrisil S, Lorthongpanich C
Role of YAP as a Mechanosensing Molecule in Stem Cells and Stem Cell-Derived Hematopoietic Cells
Damkham N et al. Role of YAP as a Mechanosensing Molecule in Stem Cells and Stem Cell-Derived Hematopoietic Cells. . 2022-11-23. Pubmed ID: 36498961; DOI: 10.3390/ijms232314634; PMC: PMC9737411 MUSIi012-AMUSIi012-A-1MUSIi012-A-2 2022-11-23 2022-11-23 PubMed: 36498961 DOI: 10.3390/ijms232314634Associated cell lines:
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Kunitomi A, Hirohata R, Arreola V, Osawa M, Kato TM, Nomura M, Kawaguchi J, Hara H, Kusano K, Takashima Y, Takahashi K, Fukuda K, Takasu N, Yamanaka S
Improved Sendai viral system for reprogramming to naive pluripotency
Kunitomi A et al. Improved Sendai viral system for reprogramming to naive pluripotency. . 2022-11-21. Pubmed ID: 36447645; DOI: 10.1016/j.crmeth.2022.100317; PMC: PMC9701587 WAe009-AKUIFMSi004-C 2022-11-21 2022-11-21 PubMed: 36447645 DOI: 10.1016/j.crmeth.2022.100317Associated cell lines:
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Cheng Fubo, Zheng Wenxu, Barbuti Peter Antony, Bonsi Paola, Liu Chang, Casadei Nicolas, Ponterio Giulia, Meringolo Maria, Admard Jakob, Dording Claire Marie, Yu-Taeger Libo, Nguyen Huu Phuc, Grundmann-Hauser Kathrin, Ott Thomas, Houlden Henry, Pisani Antonio, Krüger Rejko, Riess Olaf
DYT6 mutated THAP1 is a cell type dependent regulator of the SP1 family
Cheng Fubo et al. DYT6 mutated THAP1 is a cell type dependent regulator of the SP1 family. . 2022-11-21. DOI: 10.1093/brain/awac001 HIHDNDi001-AHIHDNDi001-B 2022-11-21 2022-11-21 DOI: 10.1093/brain/awac001Associated cell lines:
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Pawlik B, Grabia S, Smyczyńska U, Fendler W, Dróżdż I, Liszewska E, Jaworski J, Kotulska K, Jóźwiak S, Młynarski W, Trelińska J
MicroRNA Expression Profile in TSC Cell Lines and the Impact of mTOR Inhibitor
Pawlik B et al. MicroRNA Expression Profile in TSC Cell Lines and the Impact of mTOR Inhibitor. . 2022-11-21. Pubmed ID: 36430972; DOI: 10.3390/ijms232214493; PMC: PMC9694073 IIMCBi001-AIIMCBi002-A 2022-11-21 2022-11-21 PubMed: 36430972 DOI: 10.3390/ijms232214493Associated cell lines:
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Samara A, Spildrejorde M, Sharma A, Falck M, Leithaug M, Modafferi S, Bjørnstad PM, Acharya G, Gervin K, Lyle R, Eskeland R
A multi-omics approach to visualize early neuronal differentiation from hESCs in 4D
Samara A et al. A multi-omics approach to visualize early neuronal differentiation from hESCs in 4D. . 2022-11-18. Pubmed ID: 36304110; DOI: 10.1016/j.isci.2022.105279; PMC: PMC9593815 KIe009-A 2022-11-18 2022-11-18 PubMed: 36304110 DOI: 10.1016/j.isci.2022.105279Associated cell lines:
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Vázquez-Domínguez I, Duijkers L, Fadaie Z, Alaerds ECW, Post MA, van Oosten EM, O'Gorman L, Kwint M, Koolen L, Hoogendoorn ADM, Kroes HY, Gilissen C, Cremers FPM, Collin RWJ, Roosing S, Garanto A
The Predicted Splicing Variant c.11+5G>A in RPE65 Leads to a Reduction in mRNA Expression in a Cell-Specific Manner
Vázquez-Domínguez I et al. The Predicted Splicing Variant c.11+5G>A in RPE65 Leads to a Reduction in mRNA Expression in a Cell-Specific Manner. . 2022-11-17. Pubmed ID: 36429068; DOI: 10.3390/cells11223640; PMC: PMC9688607 SCTCi016-A 2022-11-17 2022-11-17 PubMed: 36429068 DOI: 10.3390/cells11223640Associated cell lines:
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Romitti M, Tourneur A, de Faria da Fonseca B, Doumont G, Gillotay P, Liao XH, Eski SE, Van Simaeys G, Chomette L, Lasolle H, Monestier O, Kasprzyk DF, Detours V, Singh SP, Goldman S, Refetoff S, Costagliola S
Transplantable human thyroid organoids generated from embryonic stem cells to rescue hypothyroidism
Romitti M et al. Transplantable human thyroid organoids generated from embryonic stem cells to rescue hypothyroidism. . 2022-11-17. Pubmed ID: 36396935; DOI: 10.1038/s41467-022-34776-7; PMC: PMC9672394 ESIBIe003-AESIBIe003-A-6 2022-11-17 2022-11-17 PubMed: 36396935 DOI: 10.1038/s41467-022-34776-7Associated cell lines:
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Vyas H, Alcheikh A, Lowe G, Stevenson WS, Morgan NV, Rabbolini DJ
Prevalence and natural history of variants in the ANKRD26 gene: a short review and update of reported cases
Vyas H et al. Prevalence and natural history of variants in the ANKRD26 gene: a short review and update of reported cases. . 2022-11-17. Pubmed ID: 35587581; DOI: 10.1080/09537104.2022.2071853; PMC: PMC9555274 SHAMUi001-A 2022-11-17 2022-11-17 PubMed: 35587581 DOI: 10.1080/09537104.2022.2071853Associated cell lines:
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de Thonel A, Ahlskog JK, Daupin K, Dubreuil V, Berthelet J, Chaput C, Pires G, Leonetti C, Abane R, Barris LC, Leray I, Aalto AL, Naceri S, Cordonnier M, Benasolo C, Sanial M, Duchateau A, Vihervaara A, Puustinen MC, Miozzo F, Fergelot P, Lebigot É, Verloes A, Gressens P, Lacombe D, Gobbo J, Garrido C, Westerheide SD, David L, Petitjean M, Taboureau O, Rodrigues-Lima F, Passemard S, Sabéran-Djoneidi D, Nguyen L, Lancaster M, Sistonen L, Mezger V
CBP-HSF2 structural and functional interplay in Rubinstein-Taybi neurodevelopmental disorder
de Thonel A et al. CBP-HSF2 structural and functional interplay in Rubinstein-Taybi neurodevelopmental disorder. . 2022-11-16. Pubmed ID: 36385105; DOI: 10.1038/s41467-022-34476-2; PMC: PMC9668993 WAe001-AWAe009-A 2022-11-16 2022-11-16 PubMed: 36385105 DOI: 10.1038/s41467-022-34476-2 -
Scharler C, Poupardin R, Ebner-Peking P, Wolf M, Schreck C, Brachtl G, Cronemberger Andrade A, Krisch L, Daheron L, Schallmoser K, Jürchott K, Küchler J, Stachelscheid H, Volk HD, Oostendorp RAJ, Strunk D
Extra-hematopoietic immunomodulatory role of the guanine-exchange factor DOCK2
Scharler C et al. Extra-hematopoietic immunomodulatory role of the guanine-exchange factor DOCK2. . 2022-11-15. Pubmed ID: 36380073; DOI: 10.1038/s42003-022-04078-1; PMC: PMC9666545 PMUi001-APMUi002-APMUi002-A-1 2022-11-15 2022-11-15 PubMed: 36380073 DOI: 10.1038/s42003-022-04078-1Associated cell lines:
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Washer SJ, Perez-Alcantara M, Chen Y, Steer J, James WS, Trynka G, Bassett AR, Cowley SA
Single-cell transcriptomics defines an improved, validated monoculture protocol for differentiation of human iPSC to microglia
Washer SJ et al. Single-cell transcriptomics defines an improved, validated monoculture protocol for differentiation of human iPSC to microglia. . 2022-11-14. Pubmed ID: 36376339; DOI: 10.1038/s41598-022-23477-2; PMC: PMC9663826 WTSIi018-BWTSIi018-B-1 2022-11-14 2022-11-14 PubMed: 36376339 DOI: 10.1038/s41598-022-23477-2Associated cell lines:
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Pospíšil J, Hrabovský M, Bohačiaková D, Hovádková Z, Jurásek M, Mlčoušková J, Paruch K, Nevolová Š, Damborsky J, Hampl A, Jaros J
Geometric Control of Cell Behavior by Biomolecule Nanodistribution
Pospíšil J et al. Geometric Control of Cell Behavior by Biomolecule Nanodistribution. . 2022-11-14. Pubmed ID: 36202388; DOI: 10.1021/acsbiomaterials.2c00650; PMC: PMC9667466 MUNIe007-A 2022-11-14 2022-11-14 PubMed: 36202388 DOI: 10.1021/acsbiomaterials.2c00650Associated cell lines:
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Ortuño-Costela MDC, Cerrada V, Moreno-Izquierdo A, García-Consuegra I, Laberthonnière C, Delourme M, Garesse R, Arenas J, Fuster García C, García García G, Millán JM, Magdinier F, Gallardo ME
Generation of the First Human In Vitro Model for McArdle Disease Based on iPSC Technology
Ortuño-Costela MDC et al. Generation of the First Human In Vitro Model for McArdle Disease Based on iPSC Technology. . 2022-11-12. Pubmed ID: 36430443; DOI: 10.3390/ijms232213964; PMC: PMC9692531 IISHDOi001-AIISHDOi002-AIISHDOi007-A 2022-11-12 2022-11-12 PubMed: 36430443 DOI: 10.3390/ijms232213964Associated cell lines:
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Farnoodian M, Bose D, Khristov V, Susaimanickam PJ, Maddileti S, Mariappan I, Abu-Asab M, Campos M, Villasmil R, Wan Q, Maminishkis A, McGaughey D, Barone F, Gundry RL, Riordon DR, Boheler KR, Sharma R, Bharti K
Cell-autonomous lipid-handling defects in Stargardt iPSC-derived retinal pigment epithelium cells
Farnoodian M et al. Cell-autonomous lipid-handling defects in Stargardt iPSC-derived retinal pigment epithelium cells. . 2022-11-08. Pubmed ID: 36306781; DOI: 10.1016/j.stemcr.2022.10.001; PMC: PMC9669500 FRIMOi003-AFRIMOi004-ALVPEIi001-ALVPEIi007-ALVPEIi008-A 2022-11-08 2022-11-08 PubMed: 36306781 DOI: 10.1016/j.stemcr.2022.10.001Associated cell lines:
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Ma J.
PLA2G6 gene related early onset Parkinson syndrome with cerebellar atrophy: 3 cases report
Ma J.. PLA2G6 gene related early onset Parkinson syndrome with cerebellar atrophy: 3 cases report. . 2022-11-08. DOI: 10.3760/cma.j.cn113694-20220720-00563 IBMSi012-A 2022-11-08 2022-11-08 DOI: 10.3760/cma.j.cn113694-20220720-00563Associated cell lines:
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Lu D, Chatterjee S, Xiao K, Riedel I, Huang CK, Costa A, Cushman S, Neufeldt D, Rode L, Schmidt A, Juchem M, Leonardy J, Büchler G, Blume J, Gern OL, Kalinke U, Wen Tan WL, Foo R, Vink A, van Laake LW, van der Meer P, Bär C, Thum T
A circular RNA derived from the insulin receptor locus protects against doxorubicin-induced cardiotoxicity
Lu D et al. A circular RNA derived from the insulin receptor locus protects against doxorubicin-induced cardiotoxicity. . 2022-11-07. Pubmed ID: 35758064; DOI: 10.1093/eurheartj/ehac337; PMC: PMC9637424 MHHi001-A 2022-11-07 2022-11-07 PubMed: 35758064 DOI: 10.1093/eurheartj/ehac337Associated cell lines:
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Cvekl A, Camerino MJ
Generation of Lens Progenitor Cells and Lentoid Bodies from Pluripotent Stem Cells: Novel Tools for Human Lens Development and Ocular Disease Etiology
Cvekl A et al. Generation of Lens Progenitor Cells and Lentoid Bodies from Pluripotent Stem Cells: Novel Tools for Human Lens Development and Ocular Disease Etiology. . 2022-11-06. Pubmed ID: 36359912; DOI: 10.3390/cells11213516; PMC: PMC9658148 SYSUSCi001-A 2022-11-06 2022-11-06 PubMed: 36359912 DOI: 10.3390/cells11213516Associated cell lines:
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Ren R, Guo J, Liu G, Kang H, Machens HG, Schilling AF, Slobodianski A, Zhang Z
Nucleic acid direct delivery to fibroblasts: a review of nucleofection and applications
Ren R et al. Nucleic acid direct delivery to fibroblasts: a review of nucleofection and applications. . 2022-11-04. Pubmed ID: 36329479; DOI: 10.1186/s13036-022-00309-5; PMC: PMC9635183 MUSIi004-A 2022-11-04 2022-11-04 PubMed: 36329479 DOI: 10.1186/s13036-022-00309-5Associated cell lines:
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Lucchino V, Scaramuzzino L, Scalise S, Lo Conte M, Zannino C, Benedetto GL, Aguglia U, Ferlazzo E, Cuda G, Parrotta EI
Insights into the Genetic Profile of Two Siblings Affected by Unverricht-Lundborg Disease Using Patient-Derived hiPSCs
Lucchino V et al. Insights into the Genetic Profile of Two Siblings Affected by Unverricht-Lundborg Disease Using Patient-Derived hiPSCs. . 2022-11-04. Pubmed ID: 36359887; DOI: 10.3390/cells11213491; PMC: PMC9655992 UNIMGi003-AUNIMGi004-A 2022-11-04 2022-11-04 PubMed: 36359887 DOI: 10.3390/cells11213491Associated cell lines:
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Kim KH, Oh J, Yang G, Lee J, Kim J, Gwak SY, Cho I, Lee SH, Byun HK, Choi HK, Kim J, Chang JS, Kang SM, Yoon HI
Association of Sinoatrial Node Radiation Dose With Atrial Fibrillation and Mortality in Patients With Lung Cancer
Kim KH et al. Association of Sinoatrial Node Radiation Dose With Atrial Fibrillation and Mortality in Patients With Lung Cancer. . 2022-11-01. Pubmed ID: 36136325; DOI: 10.1001/jamaoncol.2022.4202; PMC: PMC9501754 YCMi003-A 2022-11-01 2022-11-01 PubMed: 36136325 DOI: 10.1001/jamaoncol.2022.4202Associated cell lines:
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Gaudioso Á, Silva TP, Ledesma MD
Models to study basic and applied aspects of lysosomal storage disorders
Gaudioso Á et al. Models to study basic and applied aspects of lysosomal storage disorders. . 2022-11-00. Pubmed ID: 36122863; DOI: 10.1016/j.addr.2022.114532 TRNDi004-ITRNDi008-ATRNDi009-CUNIGEi001-APUMCi001-ASMBCi004-AAKOSi004-AAKOSi005-ANJDTHi001-AMPIi007-ASDQLCHi041-A 2022-11-00 2022-11-00 PubMed: 36122863 DOI: 10.1016/j.addr.2022.114532Associated cell lines:
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Sasserath T, Robertson AL, Mendez R, Hays TT, Smith E, Cooper H, Akanda N, Rumsey JW, Guo X, Farkhondeh A, Pradhan M, Baumgaertel K, Might M, Rodems S, Zheng W, Hickman JJ
An induced pluripotent stem cell-derived NMJ platform for study of the NGLY1-Congenital Disorder of Deglycosylation
Sasserath T et al. An induced pluripotent stem cell-derived NMJ platform for study of the NGLY1-Congenital Disorder of Deglycosylation. . 2022-11-00. Pubmed ID: 36589922; DOI: 10.1002/adtp.202200009; PMC: PMC9798846 TRNDi002-BTRNDi010-C 2022-11-00 2022-11-00 PubMed: 36589922 DOI: 10.1002/adtp.202200009Associated cell lines:
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Bakker R, Wagstaff EL, Kruijt CC, Emri E, van Karnebeek CDM, Hoffmann MB, Brooks BP, Boon CJF, Montoliu L, van Genderen MM, Bergen AA
The retinal pigmentation pathway in human albinism: Not so black and white
Bakker R et al. The retinal pigmentation pathway in human albinism: Not so black and white. . 2022-11-00. Pubmed ID: 35729001; DOI: 10.1016/j.preteyeres.2022.101091 SEIi001-A 2022-11-00 2022-11-00 PubMed: 35729001 DOI: 10.1016/j.preteyeres.2022.101091Associated cell lines:
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Vargas-Franco D, Kalra R, Draper I, Pacak CA, Asakura A, Kang PB
The Notch signaling pathway in skeletal muscle health and disease
Vargas-Franco D et al. The Notch signaling pathway in skeletal muscle health and disease. . 2022-11-00. Pubmed ID: 35968817; DOI: 10.1002/mus.27684; PMC: PMC9804383 CSCRMi001-A 2022-11-00 2022-11-00 PubMed: 35968817 DOI: 10.1002/mus.27684Associated cell lines:
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Kayumi S, Pérez-Jurado LA, Palomares M, Rangu S, Sheppard SE, Chung WK, Kruer MC, Kharbanda M, Amor DJ, McGillivray G, Cohen JS, García-Miñaúr S, van Eyk CL, Harper K, Jolly LA, Webber DL, Barnett CP, Santos-Simarro F, Pacio-Míguez M, Pozo AD, Bakhtiari S, Deardorff M, Dubbs HA, Izumi K, Grand K, Gray C, Mark PR, Bhoj EJ, Li D, Ortiz-Gonzalez XR, Keena B, Zackai EH, Goldberg EM, Perez de Nanclares G, Pereda A, Llano-Rivas I, Arroyo I, Fernández-Cuesta MÁ, Thauvin-Robinet C, Faivre L, Garde A, Mazel B, Bruel AL, Tress ML, Brilstra E, Fine AS, Crompton KE, Stegmann APA, Sinnema M, Stevens SCJ, Nicolai J, Lesca G, Lion-François L, Haye D, Chatron N, Piton A, Nizon M, Cogne B, Srivastava S, Bassetti J, Muss C, Gripp KW, Procopio RA, Millan F, Morrow MM, Assaf M, Moreno-De-Luca A, Joss S, Hamilton MJ, Bertoli M, Foulds N, McKee S, MacLennan AH, Gecz J, Corbett MA
Genomic and phenotypic characterization of 404 individuals with neurodevelopmental disorders caused by CTNNB1 variants
Kayumi S et al. Genomic and phenotypic characterization of 404 individuals with neurodevelopmental disorders caused by CTNNB1 variants. . 2022-11-00. Pubmed ID: 36083290; DOI: 10.1016/j.gim.2022.08.006; PMC: PMC9939054 SBWCHi001-A 2022-11-00 2022-11-00 PubMed: 36083290 DOI: 10.1016/j.gim.2022.08.006Associated cell lines:
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Dong M, Liu J, Liu C, Wang H, Sun W, Liu B
CRISPR/CAS9: A promising approach for the research and treatment of cardiovascular diseases
Dong M et al. CRISPR/CAS9: A promising approach for the research and treatment of cardiovascular diseases. . 2022-11-00. Pubmed ID: 36191879; DOI: 10.1016/j.phrs.2022.106480 WAe009-ALUMCi027-AWAe009-A-36UPITTi002-AUPITTi002-A-1WAe009-A-70 2022-11-00 2022-11-00 PubMed: 36191879 DOI: 10.1016/j.phrs.2022.106480Associated cell lines:
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Päth Günter, Laubner Katharina, Seufert Jochen
Stammzellen für die Wiederherstellung der endogenen Insulinsekretion
Päth Günter et al. Stammzellen für die Wiederherstellung der endogenen Insulinsekretion. . 2022-11-00. DOI: 10.1007/s11428-022-00954-w CSUASOi008-A 2022-11-00 2022-11-00 DOI: 10.1007/s11428-022-00954-wAssociated cell lines:
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Prochazka L, Michaels YS, Lau C, Jones RD, Siu M, Yin T, Wu D, Jang E, Vázquez-Cantú M, Gilbert PM, Kaul H, Benenson Y, Zandstra PW
Synthetic gene circuits for cell state detection and protein tuning in human pluripotent stem cells
Prochazka L et al. Synthetic gene circuits for cell state detection and protein tuning in human pluripotent stem cells. . 2022-11-00. Pubmed ID: 36366891; DOI: 10.15252/msb.202110886; PMC: PMC9650275 WAe001-AESIBIe002-A 2022-11-00 2022-11-00 PubMed: 36366891 DOI: 10.15252/msb.202110886Associated cell lines:
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Eremeev AV, Pikina AS, Ruchko ES, Sidorov VS, Ragozin AO
Fabrication of cartilage tissue substitutes from cells with induced pluripotency
Eremeev AV et al. Fabrication of cartilage tissue substitutes from cells with induced pluripotency. . 2022-11-00. DOI: 10.47183/mes.2022.037 RCPCMi004-A 2022-11-00 2022-11-00 DOI: 10.47183/mes.2022.037Associated cell lines:
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Song Dan, Takahashi Gou, Zheng Yun-Wen, Matsuo-Takasaki Mami, Li Jingyue, Takami Miho, An Yuri, Hemmi Yasuko, Miharada Natsumi, Fujioka Tsuyoshi, Noguchi Michiya, Nakajima Takashi, Saito Megumu K, Nakamura Yukio, Oda Tatsuya, Miyaoka Yuichiro, Hayashi Yohei
Retinoids rescue ceruloplasmin secretion and alleviate oxidative stress in Wilson’s disease-specific hepatocytes
Song Dan et al. Retinoids rescue ceruloplasmin secretion and alleviate oxidative stress in Wilson’s disease-specific hepatocytes. . 2022-10-28. DOI: 10.1093/hmg/ddac080 ZZUNEUi003-AZZUNEUi004-AZZUNEUi005-AAKOSi002-AAKOSi003-A 2022-10-28 2022-10-28 DOI: 10.1093/hmg/ddac080Associated cell lines:
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Kimura M, Iguchi T, Iwasawa K, Dunn A, Thompson WL, Yoneyama Y, Chaturvedi P, Zorn AM, Wintzinger M, Quattrocelli M, Watanabe-Chailland M, Zhu G, Fujimoto M, Kumbaji M, Kodaka A, Gindin Y, Chung C, Myers RP, Subramanian GM, Hwa V, Takebe T
En masse organoid phenotyping informs metabolic-associated genetic susceptibility to NASH
Kimura M et al. En masse organoid phenotyping informs metabolic-associated genetic susceptibility to NASH. . 2022-10-27. Pubmed ID: 36240780; DOI: 10.1016/j.cell.2022.09.031; PMC: PMC9617783 CUSTOMi001-A 2022-10-27 2022-10-27 PubMed: 36240780 DOI: 10.1016/j.cell.2022.09.031Associated cell lines:
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Carleo Giusy, Lee Yi-Shin, Secondo Agnese, Miceli Francesco, Taglialatela Maurizio
Multi-electrode array (MEASs) to investigate pathogenetic disease mechanisms and pharmacological properties in iPSC-derived neurons modelling neuropsychiatric diseases
Carleo Giusy et al. Multi-electrode array (MEASs) to investigate pathogenetic disease mechanisms and pharmacological properties in iPSC-derived neurons modelling neuropsychiatric diseases. . 2022-10-26. DOI: 10.1109/metroxraine54828.2022.9967629 UNINAi001-AUNINAi002-A 2022-10-26 2022-10-26 DOI: 10.1109/metroxraine54828.2022.9967629Associated cell lines:
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Kim J, Daadi EW, Oh T, Daadi ES, Daadi MM
Human Induced Pluripotent Stem Cell Phenotyping and Preclinical Modeling of Familial Parkinson's Disease
Kim J et al. Human Induced Pluripotent Stem Cell Phenotyping and Preclinical Modeling of Familial Parkinson's Disease. . 2022-10-25. Pubmed ID: 36360174; DOI: 10.3390/genes13111937; PMC: PMC9689743 GIBHi004-ALCSBi008-A 2022-10-25 2022-10-25 PubMed: 36360174 DOI: 10.3390/genes13111937Associated cell lines:
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Drydale Edward, Rath Phalguni, Holden Katie, Johnson Thomas, Bancroft James, Handunnetthi Lahiru
Stem cell derived neurosphere assay highlights the effects of infection on human cortical development
Drydale Edward et al. Stem cell derived neurosphere assay highlights the effects of infection on human cortical development. . 2022-10-25. DOI: 10.21203/rs.3.rs-2184467/v1 WTSIi018-B 2022-10-25 2022-10-25 DOI: 10.21203/rs.3.rs-2184467/v1Associated cell lines:
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Ondatje BN, Sances S, Workman MJ, Svendsen CN
Tissue clearing of human iPSC-derived organ-chips enables high resolution imaging and analysis
Ondatje BN et al. Tissue clearing of human iPSC-derived organ-chips enables high resolution imaging and analysis. . 2022-10-25. Pubmed ID: 36205191; DOI: 10.1039/d2lc00116k; PMC: PMC9595176 EDi028-A 2022-10-25 2022-10-25 PubMed: 36205191 DOI: 10.1039/d2lc00116kAssociated cell lines:
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Reé D, Fóthi Á, Varga N, Kolacsek O, Orbán TI, Apáti Á
Partial Disturbance of Microprocessor Function in Human Stem Cells Carrying a Heterozygous Mutation in the DGCR8 Gene
Reé D et al. Partial Disturbance of Microprocessor Function in Human Stem Cells Carrying a Heterozygous Mutation in the DGCR8 Gene. . 2022-10-23. Pubmed ID: 36360162; DOI: 10.3390/genes13111925; PMC: PMC9689658 HVRDe008-AHVRDe009-AHVRDe009-A-1HVRDe008-A-1 2022-10-23 2022-10-23 PubMed: 36360162 DOI: 10.3390/genes13111925Associated cell lines:
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Vera MB, Morris-Hanon O, Nogueiras GI, Ripari LB, Esquivel MI, Perez-Castro C, Romorini L, Sevlever GE, Scassa ME, Videla-Richardson GA
Noxa and Mcl-1 expression influence the sensitivity to BH3-mimetics that target Bcl-xL in patient-derived glioma stem cells
Vera MB et al. Noxa and Mcl-1 expression influence the sensitivity to BH3-mimetics that target Bcl-xL in patient-derived glioma stem cells. . 2022-10-22. Pubmed ID: 36273072; DOI: 10.1038/s41598-022-20910-4; PMC: PMC9587994 WAe009-AWAe009-A-51 2022-10-22 2022-10-22 PubMed: 36273072 DOI: 10.1038/s41598-022-20910-4Associated cell lines:
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Alfaar AS, Stürzbecher L, Diedrichs-Möhring M, Lam M, Roubeix C, Ritter J, Schumann K, Annamalai B, Pompös IM, Rohrer B, Sennlaub F, Reichhart N, Wildner G, Strauß O
FoxP3 expression by retinal pigment epithelial cells: transcription factor with potential relevance for the pathology of age-related macular degeneration
Alfaar AS et al. FoxP3 expression by retinal pigment epithelial cells: transcription factor with potential relevance for the pathology of age-related macular degeneration. . 2022-10-22. Pubmed ID: 36273134; DOI: 10.1186/s12974-022-02620-w; PMC: PMC9588251 CRTDi004-A 2022-10-22 2022-10-22 PubMed: 36273134 DOI: 10.1186/s12974-022-02620-wAssociated cell lines:
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Wilkens R, Hoffrichter A, Kleinsimlinghaus K, Bohl B, Haag C, Lehmann N, Schmidt M, Muñoz Perez-Vico E, Wangemann J, Rehder KF, Horschitz S, Köhr G, Ladewig J, Koch P
Diverse maturity-dependent and complementary anti-apoptotic brakes safeguard human iPSC-derived neurons from cell death
Wilkens R et al. Diverse maturity-dependent and complementary anti-apoptotic brakes safeguard human iPSC-derived neurons from cell death. . 2022-10-21. Pubmed ID: 36270985; DOI: 10.1038/s41419-022-05340-4; PMC: PMC9587001 CIMHi001-A 2022-10-21 2022-10-21 PubMed: 36270985 DOI: 10.1038/s41419-022-05340-4Associated cell lines:
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Johnson HJ, Chakraborty S, Muckom RJ, Balsara NP, Schaffer DV
A scalable and tunable thermoreversible polymer for 3D human pluripotent stem cell biomanufacturing
Johnson HJ et al. A scalable and tunable thermoreversible polymer for 3D human pluripotent stem cell biomanufacturing. . 2022-10-21. Pubmed ID: 36147944; DOI: 10.1016/j.isci.2022.104971; PMC: PMC9485071 TMOi001-A 2022-10-21 2022-10-21 PubMed: 36147944 DOI: 10.1016/j.isci.2022.104971Associated cell lines:
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Jung SY, You HJ, Kim MJ, Ko G, Lee S, Kang KS
Wnt-activating human skin organoid model of atopic dermatitis induced by Staphylococcus aureus and its protective effects by Cutibacterium acnes
Jung SY et al. Wnt-activating human skin organoid model of atopic dermatitis induced by Staphylococcus aureus and its protective effects by Cutibacterium acnes. . 2022-10-21. Pubmed ID: 36193049; DOI: 10.1016/j.isci.2022.105150; PMC: PMC9526179 KSCBi005-A 2022-10-21 2022-10-21 PubMed: 36193049 DOI: 10.1016/j.isci.2022.105150Associated cell lines:
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Peters MC, Maas RGC, van Adrichem I, Doevendans PAM, Mercola M, Šarić T, Buikema JW, van Mil A, Chamuleau SAJ, Sluijter JPG, Hnatiuk AP, Neef K
Metabolic Maturation Increases Susceptibility to Hypoxia-induced Damage in Human iPSC-derived Cardiomyocytes
Peters MC et al. Metabolic Maturation Increases Susceptibility to Hypoxia-induced Damage in Human iPSC-derived Cardiomyocytes. . 2022-10-21. Pubmed ID: 36018047; DOI: 10.1093/stcltm/szac061; PMC: PMC9585948 UKKi032-C 2022-10-21 2022-10-21 PubMed: 36018047 DOI: 10.1093/stcltm/szac061Associated cell lines:
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Durán-Alonso MB, Petković H
Induced Pluripotent Stem Cells, a Stepping Stone to In Vitro Human Models of Hearing Loss
Durán-Alonso MB et al. Induced Pluripotent Stem Cells, a Stepping Stone to In Vitro Human Models of Hearing Loss. . 2022-10-21. Pubmed ID: 36291196; DOI: 10.3390/cells11203331; PMC: PMC9600035 INMi002-AMMCi001-ATYWHSTi002-ACPGHi001-ACPGHi002-AUMi029-ACSUXHi004-ASDQLCHi035-AUMi030-ACPGHi003-ACPGHi002-A-1ZZUPMCi001-ACPGHi001-A-1KLRMMEi002-ACPGHi005-AUMi040-A 2022-10-21 2022-10-21 PubMed: 36291196 DOI: 10.3390/cells11203331 -
Völkner M, Wagner F, Steinheuer LM, Carido M, Kurth T, Yazbeck A, Schor J, Wieneke S, Ebner LJA, Del Toro Runzer C, Taborsky D, Zoschke K, Vogt M, Canzler S, Hermann A, Khattak S, Hackermüller J, Karl MO
HBEGF-TNF induce a complex outer retinal pathology with photoreceptor cell extrusion in human organoids
Völkner M et al. HBEGF-TNF induce a complex outer retinal pathology with photoreceptor cell extrusion in human organoids. . 2022-10-19. Pubmed ID: 36261438; DOI: 10.1038/s41467-022-33848-y; PMC: PMC9581928 WISCi004-BCRTDi003-ACRTDi004-A 2022-10-19 2022-10-19 PubMed: 36261438 DOI: 10.1038/s41467-022-33848-yAssociated cell lines:
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Souralova T, Rehakova D, Jeseta M, Tesarova L, Beranek J, Ventruba P, Hampl A, Koutna I
The Manufacture of Xeno- and Feeder-Free Clinical-Grade Human Embryonic Stem Cell Lines: First Step for Cell Therapy
Souralova T et al. The Manufacture of Xeno- and Feeder-Free Clinical-Grade Human Embryonic Stem Cell Lines: First Step for Cell Therapy. . 2022-10-18. Pubmed ID: 36293356; DOI: 10.3390/ijms232012500; PMC: PMC9604167 CTEFe001-ACTEFe002-ACTEFe003-A 2022-10-18 2022-10-18 PubMed: 36293356 DOI: 10.3390/ijms232012500Associated cell lines:
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Pandolfi EC, Hsu FM, Duhon M, Zheng Y, Goldsmith S, Fu J, Silber SJ, Clark AT
In vitro germ cell induction from fertile and infertile monozygotic twin research participants
Pandolfi EC et al. In vitro germ cell induction from fertile and infertile monozygotic twin research participants. . 2022-10-18. Pubmed ID: 36260988; DOI: 10.1016/j.xcrm.2022.100782; PMC: PMC9589117 UCLAi001-AUCLAi001-BUCLAi001-CUCLAi002-AUCLAi002-BUCLAi002-CUCLAi003-AUCLAi003-BUCLAi003-CUCLAi004-AUCLAi004-BUCLAi004-CUCLAi005-AUCLAi005-BUCLAi005-C 2022-10-18 2022-10-18 PubMed: 36260988 DOI: 10.1016/j.xcrm.2022.100782 -
Charoenngam N, Nasr A, Shirvani A, Holick MF
Hereditary Metabolic Bone Diseases: A Review of Pathogenesis, Diagnosis and Management
Charoenngam N et al. Hereditary Metabolic Bone Diseases: A Review of Pathogenesis, Diagnosis and Management. . 2022-10-17. Pubmed ID: 36292765; DOI: 10.3390/genes13101880; PMC: PMC9601711 SDQLCHi032-A 2022-10-17 2022-10-17 PubMed: 36292765 DOI: 10.3390/genes13101880Associated cell lines:
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Li P, Dupont B, Hu Q, Crimi M, Shen Y, Lebedev I, Liehr T
The past, present, and future for constitutional ring chromosomes: A report of the international consortium for human ring chromosomes
Li P et al. The past, present, and future for constitutional ring chromosomes: A report of the international consortium for human ring chromosomes. . 2022-10-13. Pubmed ID: 36187226; DOI: 10.1016/j.xhgg.2022.100139; PMC: PMC9519620 IMGTi001-AIMGTi001-BIMGTi003-AICGi024-AICGi025-A 2022-10-13 2022-10-13 PubMed: 36187226 DOI: 10.1016/j.xhgg.2022.100139Associated cell lines:
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Luo Elizabeth
Statistical Identification of Significant Genes to Control Chemotherapy-Induced Peripheral Neuropathy
Luo Elizabeth. Statistical Identification of Significant Genes to Control Chemotherapy-Induced Peripheral Neuropathy. . 2022-10-13. DOI: 10.1109/phm-yantai55411.2022.9942089 BIHi005-A 2022-10-13 2022-10-13 DOI: 10.1109/phm-yantai55411.2022.9942089Associated cell lines:
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Mansour F, Hinze C, Telugu NS, Kresoja J, Shaheed IB, Mosimann C, Diecke S, Schmidt-Ott KM
The centrosomal protein 83 (CEP83) regulates human pluripotent stem cell differentiation toward the kidney lineage
Mansour F et al. The centrosomal protein 83 (CEP83) regulates human pluripotent stem cell differentiation toward the kidney lineage. . 2022-10-12. Pubmed ID: 36222666; DOI: 10.7554/elife.80165; PMC: PMC9629839 WISCi004-ABIHi005-ABIHi005-A-71BIHi005-A-72BIHi005-A-73 2022-10-12 2022-10-12 PubMed: 36222666 DOI: 10.7554/elife.80165Associated cell lines:
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Vuidel A, Cousin L, Weykopf B, Haupt S, Hanifehlou Z, Wiest-Daesslé N, Segschneider M, Lee J, Kwon YJ, Peitz M, Ogier A, Brino L, Brüstle O, Sommer P, Wilbertz JH
High-content phenotyping of Parkinson's disease patient stem cell-derived midbrain dopaminergic neurons using machine learning classification
Vuidel A et al. High-content phenotyping of Parkinson's disease patient stem cell-derived midbrain dopaminergic neurons using machine learning classification. . 2022-10-11. Pubmed ID: 36179692; DOI: 10.1016/j.stemcr.2022.09.001; PMC: PMC9561636 EDi001-AEDi001-A-5 2022-10-11 2022-10-11 PubMed: 36179692 DOI: 10.1016/j.stemcr.2022.09.001Associated cell lines:
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Choe MS, Bae CM, Kim SJ, Oh ST, Kown YJ, Choi WY, Han HJ, Baek KM, Chang W, Kim JS, Lim KS, Yun SP, Lee MY
Human embryonic stem cell-specific role of YAP in maintenance of self-renewal and survival
Choe MS et al. Human embryonic stem cell-specific role of YAP in maintenance of self-renewal and survival. . 2022-10-11. Pubmed ID: 36219276; DOI: 10.1007/s00018-022-04558-x MUSIi012-AMUSIi012-A-2 2022-10-11 2022-10-11 PubMed: 36219276 DOI: 10.1007/s00018-022-04558-xAssociated cell lines:
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Wiesinger A, Li J, Fokkert L, Bakker P, Verkerk AO, Christoffels VM, Boink GJJ, Devalla HD
A single cell transcriptional roadmap of human pacemaker cell differentiation
Wiesinger A et al. A single cell transcriptional roadmap of human pacemaker cell differentiation. . 2022-10-11. Pubmed ID: 36217819; DOI: 10.7554/elife.76781; PMC: PMC9553210 LUMCi004-A 2022-10-11 2022-10-11 PubMed: 36217819 DOI: 10.7554/elife.76781Associated cell lines:
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Stüdemann T, Rössinger J, Manthey C, Geertz B, Srikantharajah R, von Bibra C, Shibamiya A, Köhne M, Wiehler A, Wiegert JS, Eschenhagen T, Weinberger F
Contractile Force of Transplanted Cardiomyocytes Actively Supports Heart Function After Injury
Stüdemann T et al. Contractile Force of Transplanted Cardiomyocytes Actively Supports Heart Function After Injury. . 2022-10-11. Pubmed ID: 36073365; DOI: 10.1161/circulationaha.122.060124; PMC: PMC9555755 UKEi001-A 2022-10-11 2022-10-11 PubMed: 36073365 DOI: 10.1161/circulationaha.122.060124Associated cell lines:
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Hovland AS, Bhattacharya D, Azambuja AP, Pramio D, Copeland J, Rothstein M, Simoes-Costa M
Pluripotency factors are repurposed to shape the epigenomic landscape of neural crest cells
Hovland AS et al. Pluripotency factors are repurposed to shape the epigenomic landscape of neural crest cells. . 2022-10-10. Pubmed ID: 36182685; DOI: 10.1016/j.devcel.2022.09.006; PMC: PMC9743141 WAe001-A 2022-10-10 2022-10-10 PubMed: 36182685 DOI: 10.1016/j.devcel.2022.09.006Associated cell lines:
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Sladen Paul E, Jovanovic Katarina, Guarascio Rosellina, Ottaviani Daniele, Salsbury Grace, Novoselova Tatiana, Chapple J Paul, Yu-Wai-Man Patrick, Cheetham Michael E
Modelling autosomal dominant optic atrophy associated with OPA1 variants in iPSC-derived retinal ganglion cells
Sladen Paul E et al. Modelling autosomal dominant optic atrophy associated with OPA1 variants in iPSC-derived retinal ganglion cells. . 2022-10-10. DOI: 10.1093/hmg/ddac128 IISHDOi003-ABIOi002-A 2022-10-10 2022-10-10 DOI: 10.1093/hmg/ddac128Associated cell lines:
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Choi S, Ferrari G, Moyle LA, Mackinlay K, Naouar N, Jalal S, Benedetti S, Wells C, Muntoni F, Tedesco FS
Assessing and enhancing migration of human myogenic progenitors using directed iPS cell differentiation and advanced tissue modelling
Choi S et al. Assessing and enhancing migration of human myogenic progenitors using directed iPS cell differentiation and advanced tissue modelling. . 2022-10-10. Pubmed ID: 36161772; DOI: 10.15252/emmm.202114526; PMC: PMC9549733 CRMi001-ACRMi003-ASBIi006-A 2022-10-10 2022-10-10 PubMed: 36161772 DOI: 10.15252/emmm.202114526 -
Zayat V, Szlendak R, Hoffman-Zacharska D
Concise Review: Stem Cell Models of SCN1A-Related Encephalopathies-Current Perspective and Future Therapies
Zayat V et al. Concise Review: Stem Cell Models of SCN1A-Related Encephalopathies-Current Perspective and Future Therapies. . 2022-10-04. Pubmed ID: 36231081; DOI: 10.3390/cells11193119; PMC: PMC9561991 FUi002-AUSTCi001-AUSTCi001-A-1USTCi001-A-2USTCi002-A 2022-10-04 2022-10-04 PubMed: 36231081 DOI: 10.3390/cells11193119Associated cell lines:
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Bajia D, Bottani E, Derwich K
Effects of Noonan Syndrome-Germline Mutations on Mitochondria and Energy Metabolism
Bajia D et al. Effects of Noonan Syndrome-Germline Mutations on Mitochondria and Energy Metabolism. . 2022-10-01. Pubmed ID: 36231062; DOI: 10.3390/cells11193099; PMC: PMC9563972 TRNDi003-A 2022-10-01 2022-10-01 PubMed: 36231062 DOI: 10.3390/cells11193099Associated cell lines:
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Huang Y, Yang J, Duan M
Auditory neuropathy: from etiology to management
Huang Y et al. Auditory neuropathy: from etiology to management. . 2022-10-01. Pubmed ID: 35939320; DOI: 10.1097/moo.0000000000000829 CPGHi003-A 2022-10-01 2022-10-01 PubMed: 35939320 DOI: 10.1097/moo.0000000000000829Associated cell lines:
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Wang H.
Research progress in treatment of epidermolysis bullosa simplex
Wang H.. Research progress in treatment of epidermolysis bullosa simplex. . 2022-10-01. DOI: 10.12144/zgmfskin202210741 UQACi001-A 2022-10-01 2022-10-01 DOI: 10.12144/zgmfskin202210741Associated cell lines:
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Mansfield C, Zhao MT, Basu M
Translational potential of hiPSCs in predictive modeling of heart development and disease
Mansfield C et al. Translational potential of hiPSCs in predictive modeling of heart development and disease. . 2022-10-01. Pubmed ID: 35261209; DOI: 10.1002/bdr2.1999; PMC: PMC9458775 ISMMSi002-BNCCDFWi001-AHDZi001-AWMUi020-ANCCDFWi001-A-1SCVIi003-ASCVIi004-ASCVIi005-AEHTJUi004-AUSFi004-ADHMi004-A 2022-10-01 2022-10-01 PubMed: 35261209 DOI: 10.1002/bdr2.1999Associated cell lines:
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Steiner T, Zink A, Henke MT, Cecchetto G, Buenning M, Rossi A, Schuelke M, Prigione A
RNA-based generation of iPSCs from a boy carrying the mutation m.9185 T>C in the mitochondrial gene MT-ATP6 and from his healthy mother
Steiner T et al. RNA-based generation of iPSCs from a boy carrying the mutation m.9185 T>C in the mitochondrial gene MT-ATP6 and from his healthy mother. . 2022-10-00. Pubmed ID: 36137325; DOI: 10.1016/j.scr.2022.102920 HHUi003-BHHUi006-AHHUi006-BHHUi003-C 2022-10-00 2022-10-00 PubMed: 36137325 DOI: 10.1016/j.scr.2022.102920 -
Wakita S, Hara M, Kitabatake Y, Kawatani K, Kurahashi H, Hashizume R
Experimental method for haplotype phasing across the entire length of chromosome 21 in trisomy 21 cells using a chromosome elimination technique
Wakita S et al. Experimental method for haplotype phasing across the entire length of chromosome 21 in trisomy 21 cells using a chromosome elimination technique. . 2022-10-00. Pubmed ID: 35637312; DOI: 10.1038/s10038-022-01049-6; PMC: PMC9510051 BGUi006-ABGUi007-A 2022-10-00 2022-10-00 PubMed: 35637312 DOI: 10.1038/s10038-022-01049-6 -
Li Y, Li Y, Liu H, Cheng L, Ma H, Xu X, Zhang N
Generation of a human induced pluripotent stem cell line (LZUSHi002-A) from a MADD patient with ETFDH mutation
Li Y et al. Generation of a human induced pluripotent stem cell line (LZUSHi002-A) from a MADD patient with ETFDH mutation. . 2022-10-00. Pubmed ID: 36162333; DOI: 10.1016/j.scr.2022.102914 LZUSHi002-A 2022-10-00 2022-10-00 PubMed: 36162333 DOI: 10.1016/j.scr.2022.102914Associated cell lines:
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Liang Y, Sun X, Duan C, Zhou Y, Cui Z, Ding C, Gu J, Mao S, Ji S, Chan HF, Tang S, Chen J
Generation of a gene-corrected human iPSC line (CSUASOi004-A-1) from a retinitis pigmentosa patient with heterozygous c.2699 G>A mutation in the PRPF6 gene
Liang Y et al. Generation of a gene-corrected human iPSC line (CSUASOi004-A-1) from a retinitis pigmentosa patient with heterozygous c.2699 G>A mutation in the PRPF6 gene. . 2022-10-00. Pubmed ID: 36103774; DOI: 10.1016/j.scr.2022.102911 CSUASOi004-ACSUASOi004-A-1 2022-10-00 2022-10-00 PubMed: 36103774 DOI: 10.1016/j.scr.2022.102911Associated cell lines:
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Chan YH, Ho CH, Tsai CY, Lu YC, Lin PH, Chen TC, Chen YT, Huang CY, Liu TC, Hsu CJ, Wu CC
Generation of induced pluripotent stem cells from a patient with hearing loss carrying OPA1 c.1468T>C (p.Cys490Arg) variant
Chan YH et al. Generation of induced pluripotent stem cells from a patient with hearing loss carrying OPA1 c.1468T>C (p.Cys490Arg) variant. . 2022-10-00. Pubmed ID: 36075118; DOI: 10.1016/j.scr.2022.102903 IBMSi026-A 2022-10-00 2022-10-00 PubMed: 36075118 DOI: 10.1016/j.scr.2022.102903Associated cell lines:
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Harper R, Yu Q, Liu Y, Yang D, Zou J, Beers J, de Jesus Rasheed AA, Goldbach-Mansky R, Boehm M, Chen G
Human induced pluripotent stem cells generated from a patient with a homozygous mutation in the Lyn kinase gene
Harper R et al. Human induced pluripotent stem cells generated from a patient with a homozygous mutation in the Lyn kinase gene. . 2022-10-00. Pubmed ID: 36215934; DOI: 10.1016/j.scr.2022.102933; PMC: PMC9674432 NIHTVBi028-A 2022-10-00 2022-10-00 PubMed: 36215934 DOI: 10.1016/j.scr.2022.102933Associated cell lines:
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Li S, He C, Feng Q, Bai Y, Liu X, Ling J, Mei L, Wu X, Feng Y, Song J
Establishment of two iPSC lines from healthy donor with heterozygous mutation in the SLC26A4 gene
Li S et al. Establishment of two iPSC lines from healthy donor with heterozygous mutation in the SLC26A4 gene. . 2022-10-00. Pubmed ID: 36126472; DOI: 10.1016/j.scr.2022.102916 CSUXHi004-ACSUXHEi001-ACSUXHEi002-A 2022-10-00 2022-10-00 PubMed: 36126472 DOI: 10.1016/j.scr.2022.102916Associated cell lines:
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Moore LR, Keller L, Paulson HL, Smith GD
Derivation of spinocerebellar ataxia type 3 human embryonic stem cell line UMICHe001-A/UM134-1
Moore LR et al. Derivation of spinocerebellar ataxia type 3 human embryonic stem cell line UMICHe001-A/UM134-1. . 2022-10-00. Pubmed ID: 35952620; DOI: 10.1016/j.scr.2022.102873; PMC: PMC10020865 UMICHe001-A 2022-10-00 2022-10-00 PubMed: 35952620 DOI: 10.1016/j.scr.2022.102873Associated cell lines:
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Zhou J, Sun Y, Wang H, Wang H, Guo F, Chen X, Gong T, Jiang C, Liang P
Generation of an induced pluripotent stem cell line (ZJULLi003-A) from a hypertrophic cardiomyopathy patient carrying MYH7/c.4384G > A mutation
Zhou J et al. Generation of an induced pluripotent stem cell line (ZJULLi003-A) from a hypertrophic cardiomyopathy patient carrying MYH7/c.4384G > A mutation. . 2022-10-00. Pubmed ID: 35944310; DOI: 10.1016/j.scr.2022.102883 ZJUi011-AZJULLi003-A 2022-10-00 2022-10-00 PubMed: 35944310 DOI: 10.1016/j.scr.2022.102883Associated cell lines:
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Okumura H, Arioka Y, Kushima I, Mori D, Ozaki N
Establishment of induced pluripotent stem cells from a patient with 16p13.11 duplication and VPS13B deletion
Okumura H et al. Establishment of induced pluripotent stem cells from a patient with 16p13.11 duplication and VPS13B deletion. . 2022-10-00. Pubmed ID: 35944312; DOI: 10.1016/j.scr.2022.102884 PNUi003-APNUi003-BPNUi003-C 2022-10-00 2022-10-00 PubMed: 35944312 DOI: 10.1016/j.scr.2022.102884 -
Keller AL, Binner A, Schenke-Layland K, Schmees C
Establishment of Four Induced Pluripotent Stem Cell Lines from CD34+ Hematopoietic Stem and Progenitor Cells from a Patient Diagnosed with an Invasive Lobular Mammary Carcinoma
Keller AL et al. Establishment of Four Induced Pluripotent Stem Cell Lines from CD34+ Hematopoietic Stem and Progenitor Cells from a Patient Diagnosed with an Invasive Lobular Mammary Carcinoma. . 2022-10-00. Pubmed ID: 36055119; DOI: 10.1016/j.scr.2022.102902 NMIi010-ANMIi011-ANMIi011-BNMIi011-CNMIi011-D 2022-10-00 2022-10-00 PubMed: 36055119 DOI: 10.1016/j.scr.2022.102902 -
Contreras J, Alonzo M, Ye S, Lin H, Hernandez-Rosario L, McBride KL, Texter K, Garg V, Zhao MT
Generation of an induced pluripotent stem cell line NCHi003-A from a 11-year-old male with pulmonary atresia with intact ventricular septum (PA-IVS)
Contreras J et al. Generation of an induced pluripotent stem cell line NCHi003-A from a 11-year-old male with pulmonary atresia with intact ventricular septum (PA-IVS). . 2022-10-00. Pubmed ID: 35987120; DOI: 10.1016/j.scr.2022.102893; PMC: PMC9629876 NCHi003-A 2022-10-00 2022-10-00 PubMed: 35987120 DOI: 10.1016/j.scr.2022.102893Associated cell lines:
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Wang Y, Lv Y, Yang X, Li Y, Li Z, Gao Z, Gai Z, Liu Y
Generation of an induced pluripotent stem cell line (SDQLCHi044-A) from a patient with autosomal dominant mental retardation type 5 harboring heterozygous mutation in SYNGAP1 gene
Wang Y et al. Generation of an induced pluripotent stem cell line (SDQLCHi044-A) from a patient with autosomal dominant mental retardation type 5 harboring heterozygous mutation in SYNGAP1 gene. . 2022-10-00. Pubmed ID: 36183676; DOI: 10.1016/j.scr.2022.102922 SDQLCHi044-A 2022-10-00 2022-10-00 PubMed: 36183676 DOI: 10.1016/j.scr.2022.102922Associated cell lines:
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Leeson HC, Goh D, Coman D, Wolvetang EJ
Generation of iPSC lines from hereditary spastic paraplegia 56 (SPG56) patients and family members carrying CYP2U1 mutations
Leeson HC et al. Generation of iPSC lines from hereditary spastic paraplegia 56 (SPG56) patients and family members carrying CYP2U1 mutations. . 2022-10-00. Pubmed ID: 36166872; DOI: 10.1016/j.scr.2022.102917 AIBNi015-AAIBNi016-AAIBNi017-AAIBNi018-A 2022-10-00 2022-10-00 PubMed: 36166872 DOI: 10.1016/j.scr.2022.102917Associated cell lines:
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Tian L, Zhang XH, Xu K, Li Y
Induced pluripotent stem cell line BIOi003-A from a patient with ABCA4-associated retinal dystrophy carrying compound heterozygous c.(1222C>T;2919-884G>T) variants in ABCA4
Tian L et al. Induced pluripotent stem cell line BIOi003-A from a patient with ABCA4-associated retinal dystrophy carrying compound heterozygous c.(1222C>T;2919-884G>T) variants in ABCA4. . 2022-10-00. Pubmed ID: 35973334; DOI: 10.1016/j.scr.2022.102894 BIOi002-ABIOi003-A 2022-10-00 2022-10-00 PubMed: 35973334 DOI: 10.1016/j.scr.2022.102894 -
Schröter J, Syring H, Göhring G, Kölker S, Opladen T, Hoffmann GF, Syrbe S, Jung-Klawitter S
Generation of an induced pluripotent stem cell line (DHMCi009-A) from an individual with TUBB2A tubulinopathy
Schröter J et al. Generation of an induced pluripotent stem cell line (DHMCi009-A) from an individual with TUBB2A tubulinopathy. . 2022-10-00. Pubmed ID: 35930870; DOI: 10.1016/j.scr.2022.102879 DHMCi009-A 2022-10-00 2022-10-00 PubMed: 35930870 DOI: 10.1016/j.scr.2022.102879Associated cell lines:
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Pera J, Castaño J, Casamitjana J, Giorgetti A, Romero-Moya D
Generation of heterozygous SAMD9 CRISPR/Cas9-edited iPSC line (ESi086-A-3), carrying p.I1567M mutation
Pera J et al. Generation of heterozygous SAMD9 CRISPR/Cas9-edited iPSC line (ESi086-A-3), carrying p.I1567M mutation. . 2022-10-00. Pubmed ID: 36087523; DOI: 10.1016/j.scr.2022.102906 ESi086-AESi086-A-3 2022-10-00 2022-10-00 PubMed: 36087523 DOI: 10.1016/j.scr.2022.102906Associated cell lines:
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Zhou M, Huang P, Bai R, Liu X
Generation of a homozygous TAZ knockout hESCs line by CRISPR/Cas9 system
Zhou M et al. Generation of a homozygous TAZ knockout hESCs line by CRISPR/Cas9 system. . 2022-10-00. Pubmed ID: 36219982; DOI: 10.1016/j.scr.2022.102923 WAe009-AWAe009-A-36WAe009-A-91 2022-10-00 2022-10-00 PubMed: 36219982 DOI: 10.1016/j.scr.2022.102923Associated cell lines:
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Lin Z, Cheng H, Zhang Y, Zheng B, Zhang F, Lin Y, Zhu Y, Ju W, Cui C, Chen M
Generation of a human induced pluripotent stem cell line (JSPHi003-A) from a patient with atrial fibrillation and ventricular tachycardia carrying LMNA frame shift mutation (c.1304_1307dup)
Lin Z et al. Generation of a human induced pluripotent stem cell line (JSPHi003-A) from a patient with atrial fibrillation and ventricular tachycardia carrying LMNA frame shift mutation (c.1304_1307dup). . 2022-10-00. Pubmed ID: 36095892; DOI: 10.1016/j.scr.2022.102909 JSPHi003-A 2022-10-00 2022-10-00 PubMed: 36095892 DOI: 10.1016/j.scr.2022.102909Associated cell lines:
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Latoszek E, Piechota M, Liszewska E, Hansíková H, Klempíř J, Mühlbäck A, Landwehrmeyer GB, Kuznicki J, Czeredys M
Generation of three human iPSC lines from patients with Huntington's disease with different CAG lengths and human control iPSC line from a healthy donor
Latoszek E et al. Generation of three human iPSC lines from patients with Huntington's disease with different CAG lengths and human control iPSC line from a healthy donor. . 2022-10-00. Pubmed ID: 36228511; DOI: 10.1016/j.scr.2022.102931 IIMCBi001-AIIMCBi002-AIIMCBi003-AIIMCBi004-AIIMCBi005-AIIMCBi006-A 2022-10-00 2022-10-00 PubMed: 36228511 DOI: 10.1016/j.scr.2022.102931Associated cell lines:
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Takamatsu G, Manome Y, Lee JS, Toyama K, Hayakawa T, Hara-Miyauchi C, Hasegawa-Ogawa M, Katagiri C, Kondo T, James Okano H, Matsushita M
Generation of four iPSC lines from a family harboring a 1p36-35 haplotype linked with bipolar disorder and recurrent depressive disorder: Three-generation patients and a healthy sibling
Takamatsu G et al. Generation of four iPSC lines from a family harboring a 1p36-35 haplotype linked with bipolar disorder and recurrent depressive disorder: Three-generation patients and a healthy sibling. . 2022-10-00. Pubmed ID: 36166871; DOI: 10.1016/j.scr.2022.102915 URi001-AURi002-AURi004-AURi005-A 2022-10-00 2022-10-00 PubMed: 36166871 DOI: 10.1016/j.scr.2022.102915 -
Kojic A, Kim H, Guevara JV, Ravada S, Sallam K, Wu JC
Generation of two induced pluripotent stem cell lines from dilated cardiomyopathy patients carrying heterozygous FLNC mutations
Kojic A et al. Generation of two induced pluripotent stem cell lines from dilated cardiomyopathy patients carrying heterozygous FLNC mutations. . 2022-10-00. Pubmed ID: 36194907; DOI: 10.1016/j.scr.2022.102928; PMC: PMC10871033 SCVIi059-ASCVIi060-A 2022-10-00 2022-10-00 PubMed: 36194907 DOI: 10.1016/j.scr.2022.102928Associated cell lines:
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You J, Ma S, Zhang H, Chen L
Generation of a homozygous P4HA2 knockout human embryonic stem cell line (FDCHDPe012-A) by CRISPR/Cas9 system
You J et al. Generation of a homozygous P4HA2 knockout human embryonic stem cell line (FDCHDPe012-A) by CRISPR/Cas9 system. . 2022-10-00. Pubmed ID: 36206672; DOI: 10.1016/j.scr.2022.102930 WAe009-A-56WAe009-A-J 2022-10-00 2022-10-00 PubMed: 36206672 DOI: 10.1016/j.scr.2022.102930Associated cell lines:
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Ahmad I, Goel D, Ghosh A, Kapoor H, Kumar D, Srivastava AK, Faruq M
Lab resource: Single cell line generation and characterization of a human-derived induced pluripotent stem cell line (IGIBi005-A) from a patient with spastic paraplegia/ataxia/ALS phenotype due to the mutation of the gene Kinesin Family Member 5A (KIF5A)
Ahmad I et al. Lab resource: Single cell line generation and characterization of a human-derived induced pluripotent stem cell line (IGIBi005-A) from a patient with spastic paraplegia/ataxia/ALS phenotype due to the mutation of the gene Kinesin Family Member 5A (KIF5A). . 2022-10-00. Pubmed ID: 36055117; DOI: 10.1016/j.scr.2022.102904 IGIBi005-AIGIBi007-A 2022-10-00 2022-10-00 PubMed: 36055117 DOI: 10.1016/j.scr.2022.102904Associated cell lines:
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Pinto MAF, Ferreira CBR, de Lima BES, Molon ÂC, Ibarra AMC, Cecatto RB, Dos Santos Franco AL, Rodrigues MFSD
Effects of 5-ALA mediated photodynamic therapy in oral cancer stem cells
Pinto MAF et al. Effects of 5-ALA mediated photodynamic therapy in oral cancer stem cells. . 2022-10-00. Pubmed ID: 36088836; DOI: 10.1016/j.jphotobiol.2022.112552 MSHRIe001-A 2022-10-00 2022-10-00 PubMed: 36088836 DOI: 10.1016/j.jphotobiol.2022.112552Associated cell lines:
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X-Q Chen C, Deneault E, Abdian N, You Z, Sirois J, Nicouleau M, Shlaifer I, Villegas L, Boivin MN, Gaborieau L, Karamchandani J, Beitel LK, Fon EA, Durcan TM
Generation of patient-derived pluripotent stem cell-lines and CRISPR modified isogenic controls with mutations in the Parkinson's associated GBA gene
X-Q Chen C et al. Generation of patient-derived pluripotent stem cell-lines and CRISPR modified isogenic controls with mutations in the Parkinson's associated GBA gene. . 2022-10-00. Pubmed ID: 36130446; DOI: 10.1016/j.scr.2022.102919 CBIGi002-ACBIGi002-A-1CBIGi003-ACBIGi003-A-1 2022-10-00 2022-10-00 PubMed: 36130446 DOI: 10.1016/j.scr.2022.102919Associated cell lines:
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Hänchen V, Kretschmer S, Wolf C, Engel K, Khattak S, Neumann K, Lee-Kirsch MA
Generation of induced pluripotent stem cell lines from three patients with Aicardi-Goutières syndrome type 5 due to biallelic SAMDH1 mutations
Hänchen V et al. Generation of induced pluripotent stem cell lines from three patients with Aicardi-Goutières syndrome type 5 due to biallelic SAMDH1 mutations. . 2022-10-00. Pubmed ID: 36115319; DOI: 10.1016/j.scr.2022.102912 CRTDi009-ACRTDi008-BCRTDi010-B 2022-10-00 2022-10-00 PubMed: 36115319 DOI: 10.1016/j.scr.2022.102912Associated cell lines:
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Zhang P, Wang H, Li S, Guo T, Zhang R, Zhou P, Ding S
Generation of an S100B homozygous knockout pluripotent stem cell line (WAe009-A-94) by the CRISPR/Cas9 system
Zhang P et al. Generation of an S100B homozygous knockout pluripotent stem cell line (WAe009-A-94) by the CRISPR/Cas9 system. . 2022-10-00. Pubmed ID: 36182708; DOI: 10.1016/j.scr.2022.102924 WAe009-AWAe009-A-94 2022-10-00 2022-10-00 PubMed: 36182708 DOI: 10.1016/j.scr.2022.102924Associated cell lines:
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Xu P, Guo F, Xie B, Zhong X
Generation and characterization of two iPSC lines carrying heterozygous or homozygous nonsense mutation in PROM1 gene from a single family
Xu P et al. Generation and characterization of two iPSC lines carrying heterozygous or homozygous nonsense mutation in PROM1 gene from a single family. . 2022-10-00. Pubmed ID: 36191543; DOI: 10.1016/j.scr.2022.102913 SKLOi002-ASKLOi003-A 2022-10-00 2022-10-00 PubMed: 36191543 DOI: 10.1016/j.scr.2022.102913Associated cell lines:
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Alonzo M, Contreras J, Ye S, Lin H, Hernandez-Rosario L, McBride KL, Texter K, Garg V, Zhao MT
Characterization of an iPSC line NCHi006-A from a patient with hypoplastic left heart syndrome (HLHS)
Alonzo M et al. Characterization of an iPSC line NCHi006-A from a patient with hypoplastic left heart syndrome (HLHS). . 2022-10-00. Pubmed ID: 35987121; DOI: 10.1016/j.scr.2022.102892; PMC: PMC9614611 NCHi006-A 2022-10-00 2022-10-00 PubMed: 35987121 DOI: 10.1016/j.scr.2022.102892Associated cell lines:
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Wu K, Takanohashi A, Woidill S, Seylani A, Helman G, Dias P, Beers J, Lin Y, Simons C, Wolvetang E, Zou J, Vanderver A, Sack MN
Generation of human induced pluripotential stem cells from individuals with complex heterozygous, isogenic corrected, and homozygous Bloc1s1 mutations
Wu K et al. Generation of human induced pluripotential stem cells from individuals with complex heterozygous, isogenic corrected, and homozygous Bloc1s1 mutations. . 2022-10-00. Pubmed ID: 36070637; DOI: 10.1016/j.scr.2022.102905 NIHTVBi019-ANIHTVBi020-ANIHTVBi021-ANIHTVBi022-ANIHTVBi019-A-1 2022-10-00 2022-10-00 PubMed: 36070637 DOI: 10.1016/j.scr.2022.102905Associated cell lines:
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Heider J, Sperlich D, Vogel S, Breitmeyer R, Volkmer H
Generation of two induced pluripotent stem cell lines (TMOi001-A-5, TMOi001-A-6) carrying variants in DISC1 exon 2 using CRISPR/Cas9 gene editing
Heider J et al. Generation of two induced pluripotent stem cell lines (TMOi001-A-5, TMOi001-A-6) carrying variants in DISC1 exon 2 using CRISPR/Cas9 gene editing. . 2022-10-00. Pubmed ID: 36154917; DOI: 10.1016/j.scr.2022.102925 TMOi001-ATMOi001-A-5TMOi001-A-6 2022-10-00 2022-10-00 PubMed: 36154917 DOI: 10.1016/j.scr.2022.102925Associated cell lines:
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Nist-Lund C, Kim J, Koehler KR
Advancements in inner ear development, regeneration, and repair through otic organoids
Nist-Lund C et al. Advancements in inner ear development, regeneration, and repair through otic organoids. . 2022-10-00. Pubmed ID: 35853286; DOI: 10.1016/j.gde.2022.101954; PMC: PMC10425989 CPGHi001-ACPGHi001-A-1 2022-10-00 2022-10-00 PubMed: 35853286 DOI: 10.1016/j.gde.2022.101954Associated cell lines:
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Pratumkaew P, Luanpitpong S, Klaihmon P, Lorthongpanich C, Laowtammathron C, Meesa S, Suksomboon W, Issaragrisil S
Episomal vector-based generation of human induced pluripotent stem cell line MUSIi020-A from peripheral blood T-cells
Pratumkaew P et al. Episomal vector-based generation of human induced pluripotent stem cell line MUSIi020-A from peripheral blood T-cells. . 2022-10-00. Pubmed ID: 36183677; DOI: 10.1016/j.scr.2022.102929 MUSIi020-A 2022-10-00 2022-10-00 PubMed: 36183677 DOI: 10.1016/j.scr.2022.102929Associated cell lines:
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Panchuk I, Kondrateva E, Demchenko A, Grigorieva O, Erofeeva A, Amelina E, Tabakov V, Orlova M, Voronina E, Pozhitnova V, Lavrov A, Smirnikhina S, Kutsev S
Generation of two induced pluripotent stem cell lines (RCMGi005-A/B) from human skin fibroblasts of a cystic fibrosis patient with homozygous F508del mutation in CFTR gene
Panchuk I et al. Generation of two induced pluripotent stem cell lines (RCMGi005-A/B) from human skin fibroblasts of a cystic fibrosis patient with homozygous F508del mutation in CFTR gene. . 2022-10-00. Pubmed ID: 36067639; DOI: 10.1016/j.scr.2022.102896 RCMGi005-ARCMGi005-B 2022-10-00 2022-10-00 PubMed: 36067639 DOI: 10.1016/j.scr.2022.102896Associated cell lines:
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Coutier J, Bonnette M, Martineau S, Mercadier A, Domingues S, Saidani M, Jarrige M, Polveche H, Darle A, Holic N, Hadj-Rabia S, Bodemer C, Lemaitre G, Martinat C, Baldeschi C
Human-Induced Pluripotent Stem Cell‒Derived Keratinocytes, a Useful Model to Identify and Explore the Pathological Phenotype of Epidermolysis Bullosa Simplex
Coutier J et al. Human-Induced Pluripotent Stem Cell‒Derived Keratinocytes, a Useful Model to Identify and Explore the Pathological Phenotype of Epidermolysis Bullosa Simplex. . 2022-10-00. Pubmed ID: 35490743; DOI: 10.1016/j.jid.2022.04.009 UQACi001-A 2022-10-00 2022-10-00 PubMed: 35490743 DOI: 10.1016/j.jid.2022.04.009Associated cell lines:
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Nam KH, Ordureau A
Quantitative proteome remodeling characterization of two human reference pluripotent stem cell lines during neurogenesis and cardiomyogenesis
Nam KH et al. Quantitative proteome remodeling characterization of two human reference pluripotent stem cell lines during neurogenesis and cardiomyogenesis. . 2022-10-00. Pubmed ID: 35871287; DOI: 10.1002/pmic.202100246; PMC: PMC10389174 WAe009-A 2022-10-00 2022-10-00 PubMed: 35871287 DOI: 10.1002/pmic.202100246Associated cell lines:
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Bulut M, Vila Cuenca M, de Graaf M, van den Hil FE, Mummery CL, Orlova VV
Three-Dimensional Vessels-on-a-Chip Based on hiPSC-derived Vascular Endothelial and Smooth Muscle Cells
Bulut M et al. Three-Dimensional Vessels-on-a-Chip Based on hiPSC-derived Vascular Endothelial and Smooth Muscle Cells. . 2022-10-00. Pubmed ID: 36250774; DOI: 10.1002/cpz1.564 CRMi003-ALUMCi001-AUCSFi001-AUCSFi001-A-3 2022-10-00 2022-10-00 PubMed: 36250774 DOI: 10.1002/cpz1.564Associated cell lines:
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Yang M, Fu JD, Zou J, Sridharan D, Zhao MT, Singh H, Krigman J, Khan M, Xin G, Sun N
Assessment of mitophagy in human iPSC-derived cardiomyocytes
Yang M et al. Assessment of mitophagy in human iPSC-derived cardiomyocytes. . 2022-10-00. Pubmed ID: 35220905; DOI: 10.1080/15548627.2022.2037920; PMC: PMC9542630 NHLBIi001-ANHLBIi001-BNHLBIi003-ANHLBIi003-A-1NHLBIi003-A-2 2022-10-00 2022-10-00 PubMed: 35220905 DOI: 10.1080/15548627.2022.2037920Associated cell lines:
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Srivastava A, Siwach I, Rockman-Greenberg C, Dhingra S
Reprogramming of Hypophosphatasia patient cells to generate a new human iPSC cell line (UOMi009-A)
Srivastava A et al. Reprogramming of Hypophosphatasia patient cells to generate a new human iPSC cell line (UOMi009-A). . 2022-10-00. Pubmed ID: 36152425; DOI: 10.1016/j.scr.2022.102921 UOMi005-AUOMi006-AUOMi009-A 2022-10-00 2022-10-00 PubMed: 36152425 DOI: 10.1016/j.scr.2022.102921 -
Sen T, Thummer RP
CRISPR and iPSCs: Recent Developments and Future Perspectives in Neurodegenerative Disease Modelling, Research, and Therapeutics
Sen T et al. CRISPR and iPSCs: Recent Developments and Future Perspectives in Neurodegenerative Disease Modelling, Research, and Therapeutics. . 2022-10-00. Pubmed ID: 36044181; DOI: 10.1007/s12640-022-00564-w; PMC: PMC9428373 NHLBIi003-ANHLBIi003-A-1NHLBIi003-A-2UMi028-AUMi028-A-2JHUi003-A 2022-10-00 2022-10-00 PubMed: 36044181 DOI: 10.1007/s12640-022-00564-wAssociated cell lines:
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Ahmad I, Goel D, Ghosh A, Kapoor H, Kumar D, Ramesh K, Ashley B, Deepika K, Shastry A, Faruq M
Generation of two induced pluripotent stem cell (iPSC) lines from patients with Duchenne muscular dystrophy (IGIBi006-A and IGIBi008-A) carrying exonic deletions in the dystrophin gene
Ahmad I et al. Generation of two induced pluripotent stem cell (iPSC) lines from patients with Duchenne muscular dystrophy (IGIBi006-A and IGIBi008-A) carrying exonic deletions in the dystrophin gene. . 2022-10-00. Pubmed ID: 36191544; DOI: 10.1016/j.scr.2022.102927 IGIBi006-AIGIBi008-A 2022-10-00 2022-10-00 PubMed: 36191544 DOI: 10.1016/j.scr.2022.102927Associated cell lines:
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Nayak R, Rosh I, Rabinski T, Falik D, Mendel Percia M, Stern S
Generation and characterization of iPSC lines (UOHi003-A, UOHi002-A) from a patient with SHANK3 mutation and her healthy mother
Nayak R et al. Generation and characterization of iPSC lines (UOHi003-A, UOHi002-A) from a patient with SHANK3 mutation and her healthy mother. . 2022-10-00. Pubmed ID: 36044808; DOI: 10.1016/j.scr.2022.102899 UOHi002-AUOHi003-A 2022-10-00 2022-10-00 PubMed: 36044808 DOI: 10.1016/j.scr.2022.102899 -
Ura H, Togi S, Hatanaka H, Niida Y
Establishment of a human induced pluripotent stem cell line, KMUGMCi005-A, from a patient with Epidermodysplasia verruciformis (EV) bearing homozygous splicing donor site mutation in the TMC8 gene
Ura H et al. Establishment of a human induced pluripotent stem cell line, KMUGMCi005-A, from a patient with Epidermodysplasia verruciformis (EV) bearing homozygous splicing donor site mutation in the TMC8 gene. . 2022-10-00. Pubmed ID: 36170758; DOI: 10.1016/j.scr.2022.102926 KMUGMCi005-A 2022-10-00 2022-10-00 PubMed: 36170758 DOI: 10.1016/j.scr.2022.102926Associated cell lines:
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Huang YZ, He T, Cui J, Jiang YL, Zeng JF, Zhang WQ, Xie HQ
Urine-Derived Stem Cells for Regenerative Medicine: Basic Biology, Applications, and Challenges
Huang YZ et al. Urine-Derived Stem Cells for Regenerative Medicine: Basic Biology, Applications, and Challenges. . 2022-10-00. Pubmed ID: 35049395; DOI: 10.1089/ten.teb.2021.0142 ZZUNEUi022-ACSUXHi005-A 2022-10-00 2022-10-00 PubMed: 35049395 DOI: 10.1089/ten.teb.2021.0142Associated cell lines:
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Rovina D, Castiglioni E, Mallia S, Rabino M, Farini A, Belicchi M, Di Giuseppe G, Gervasini C, Torrente Y, Pompilio G, Gowran A
Reprogramming of dermal fibroblasts from a Duchenne muscular dystrophy patient carrying a deletion of exons 45-50 into an induced pluripotent stem cell line (CCMi005-A)
Rovina D et al. Reprogramming of dermal fibroblasts from a Duchenne muscular dystrophy patient carrying a deletion of exons 45-50 into an induced pluripotent stem cell line (CCMi005-A). . 2022-10-00. Pubmed ID: 35961103; DOI: 10.1016/j.scr.2022.102889 CCMi005-A 2022-10-00 2022-10-00 PubMed: 35961103 DOI: 10.1016/j.scr.2022.102889Associated cell lines:
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Ura H, Togi S, Hatanaka H, Niida Y
Establishment of a human induced pluripotent stem cell line, KMUGMCi003-A, from a patient with trichothiodystrophy 1 (TTD1) bearing compound heterozygous missense mutations in the ERCC2 gene
Ura H et al. Establishment of a human induced pluripotent stem cell line, KMUGMCi003-A, from a patient with trichothiodystrophy 1 (TTD1) bearing compound heterozygous missense mutations in the ERCC2 gene. . 2022-10-00. Pubmed ID: 35944311; DOI: 10.1016/j.scr.2022.102885 KMUGMCi003-A 2022-10-00 2022-10-00 PubMed: 35944311 DOI: 10.1016/j.scr.2022.102885Associated cell lines:
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Wolnik J, Kubiak G, Skoczyńska M, Wiland P, Fearon U, Veale D, Dulak J, Biniecka M
Generation of two hiPSC lines, (DMBi003-A and DMBi004-A), by reprogramming peripheral blood mononuclear cells and fibroblast-like synoviocytes from rheumatoid arthritis patients
Wolnik J et al. Generation of two hiPSC lines, (DMBi003-A and DMBi004-A), by reprogramming peripheral blood mononuclear cells and fibroblast-like synoviocytes from rheumatoid arthritis patients. . 2022-10-00. Pubmed ID: 35973333; DOI: 10.1016/j.scr.2022.102886 DMBi003-ADMBi004-A 2022-10-00 2022-10-00 PubMed: 35973333 DOI: 10.1016/j.scr.2022.102886 -
Huang W, Zhou Y, Wang J, Jiang C, Zhang Y, Zhou R
Generation of two heterozygous GAA mutation-carrying human induced pluripotent stem cell lines (XACHi005-A, XACHi006-A) from parents of an infant with Pompe disease
Huang W et al. Generation of two heterozygous GAA mutation-carrying human induced pluripotent stem cell lines (XACHi005-A, XACHi006-A) from parents of an infant with Pompe disease. . 2022-10-00. Pubmed ID: 36240644; DOI: 10.1016/j.scr.2022.102934 XACHi005-AXACHi006-A 2022-10-00 2022-10-00 PubMed: 36240644 DOI: 10.1016/j.scr.2022.102934Associated cell lines:
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Jiang Z, Gu XJ, Su WM, Duan QQ, Lin JY, Cao B, Shang HF, Chen YP
Production of a human iPSC line from an early-onset Parkinson's disease patient with a novel CHCHD2 gene truncated mutation
Jiang Z et al. Production of a human iPSC line from an early-onset Parkinson's disease patient with a novel CHCHD2 gene truncated mutation. . 2022-10-00. Pubmed ID: 35944313; DOI: 10.1016/j.scr.2022.102881 WCHSCUi001-A 2022-10-00 2022-10-00 PubMed: 35944313 DOI: 10.1016/j.scr.2022.102881Associated cell lines:
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Velchev JD, Verstraeten A, Meester J, Ponsaerts P, Richer J, Alaerts M, Loeys B
Generation and validation of an iPSC line (BBANTWi008-A) from a Loeys-Dietz Syndrome type 3 patient
Velchev JD et al. Generation and validation of an iPSC line (BBANTWi008-A) from a Loeys-Dietz Syndrome type 3 patient. . 2022-10-00. Pubmed ID: 36219981; DOI: 10.1016/j.scr.2022.102932 BBANTWi006-ABBANTWi007-ABBANTWi008-A 2022-10-00 2022-10-00 PubMed: 36219981 DOI: 10.1016/j.scr.2022.102932Associated cell lines:
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Zhen X, Kang W, Park SJ, Choe SH, Hong SH, Lee DS, Lee JH
Generation and characterization of cynomolgus monkey kidney fibroblasts (cmKF)-derived induced pluripotent stem cells (cmKF-iPS-C5)
Zhen X et al. Generation and characterization of cynomolgus monkey kidney fibroblasts (cmKF)-derived induced pluripotent stem cells (cmKF-iPS-C5). . 2022-10-00. Pubmed ID: 35944314; DOI: 10.1016/j.scr.2022.102887 KRIBBi005-A 2022-10-00 2022-10-00 PubMed: 35944314 DOI: 10.1016/j.scr.2022.102887Associated cell lines:
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Srivastava A, Verma E, Rockman-Greenberg C, Dhingra S
Generation of new human iPSC cell line (UOMi008-A) from a Hypophosphatasia patient
Srivastava A et al. Generation of new human iPSC cell line (UOMi008-A) from a Hypophosphatasia patient. . 2022-10-00. Pubmed ID: 35964540; DOI: 10.1016/j.scr.2022.102891 UOMi005-AUOMi006-AUOMi008-A 2022-10-00 2022-10-00 PubMed: 35964540 DOI: 10.1016/j.scr.2022.102891 -
Avdili A, Rohrhofer L, Auer M, Bernecker C, Schlenke P, Dorn I
Generation of the human erythroblast-derived iPSC line UBTi001-A
Avdili A et al. Generation of the human erythroblast-derived iPSC line UBTi001-A. . 2022-10-00. Pubmed ID: 36103773; DOI: 10.1016/j.scr.2022.102910 UBTi001-A 2022-10-00 2022-10-00 PubMed: 36103773 DOI: 10.1016/j.scr.2022.102910Associated cell lines:
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Sun Y, Zhou J, Wang H, Wang H, Chen X, Gong T, Liang P, Jiang C
Establishment of an induced pluripotent stem cell line (ZJULLi004-A) from a hypertrophic cardiomyopathy patient carrying MYBPC3/c.3764C>A mutation
Sun Y et al. Establishment of an induced pluripotent stem cell line (ZJULLi004-A) from a hypertrophic cardiomyopathy patient carrying MYBPC3/c.3764C>A mutation. . 2022-10-00. Pubmed ID: 36041398; DOI: 10.1016/j.scr.2022.102898 ZJUi012-AZJULLi004-A 2022-10-00 2022-10-00 PubMed: 36041398 DOI: 10.1016/j.scr.2022.102898Associated cell lines:
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Hänchen V, Kretschmer S, Wolf C, Engel K, Khattak S, Neumann K, Lee-Kirsch MA
Generation of induced pluripotent stem cell lines from two patients with Aicardi-Goutières syndrome type 1 due to biallelic TREX1 mutations
Hänchen V et al. Generation of induced pluripotent stem cell lines from two patients with Aicardi-Goutières syndrome type 1 due to biallelic TREX1 mutations. . 2022-10-00. Pubmed ID: 36027857; DOI: 10.1016/j.scr.2022.102895 CRTDi006-ACRTDi006-BCRTDi007-ACRTDi007-B 2022-10-00 2022-10-00 PubMed: 36027857 DOI: 10.1016/j.scr.2022.102895Associated cell lines:
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Chen L, Zhang J, Yang X, Wang S, Ye F
Generation of human induced pluripotent stem cell lines SPPHIi003-A and SPPHIi004-A from two patients with sporadic Alzheimer's disease in Southwestern China
Chen L et al. Generation of human induced pluripotent stem cell lines SPPHIi003-A and SPPHIi004-A from two patients with sporadic Alzheimer's disease in Southwestern China. . 2022-10-00. Pubmed ID: 35933956; DOI: 10.1016/j.scr.2022.102876 SPPHIi003-ASPPHIi004-A 2022-10-00 2022-10-00 PubMed: 35933956 DOI: 10.1016/j.scr.2022.102876Associated cell lines:
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Wu S, Deng H, Lu B, Yuan L, Wang X
Generation of CD16A gene knockout human embryonic stem cell line using CRISPR/Cas9
Wu S et al. Generation of CD16A gene knockout human embryonic stem cell line using CRISPR/Cas9. . 2022-10-00. Pubmed ID: 36219983; DOI: 10.1016/j.scr.2022.102935 WAe001-A-81 2022-10-00 2022-10-00 PubMed: 36219983 DOI: 10.1016/j.scr.2022.102935Associated cell lines:
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Jaboreck MC, Lühmann JL, Mielenz M, Stanke F, Göhring G, Martin U, Olmer R, Merkert S
Generation of two TMEM16A knockout iPSC clones each from a healthy human iPSC line, from a Cystic Fibrosis patient specific line with p.Phe508del mutation and from the gene corrected iPSC line
Jaboreck MC et al. Generation of two TMEM16A knockout iPSC clones each from a healthy human iPSC line, from a Cystic Fibrosis patient specific line with p.Phe508del mutation and from the gene corrected iPSC line. . 2022-10-00. Pubmed ID: 36162332; DOI: 10.1016/j.scr.2022.102918 MHHi001-AMHHi002-AMHHi002-A-1MHHi001-A-1MHHi001-A-2MHHi002-A-4MHHi002-A-5MHHi002-A-6MHHi002-A-7 2022-10-00 2022-10-00 PubMed: 36162332 DOI: 10.1016/j.scr.2022.102918Associated cell lines:
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Kang JY, Mun D, Chun Y, Park DS, Kim H, Yun N, Lee SH, Joung B
Generation of three TTN knock-out human induced pluripotent stem cell lines using CRISPR/Cas9 system
Kang JY et al. Generation of three TTN knock-out human induced pluripotent stem cell lines using CRISPR/Cas9 system. . 2022-10-00. Pubmed ID: 36037555; DOI: 10.1016/j.scr.2022.102901 KSCBi018-A-3KSCBi018-A-4KSCBi018-A-5 2022-10-00 2022-10-00 PubMed: 36037555 DOI: 10.1016/j.scr.2022.102901Associated cell lines:
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Liu J, Black GC, Kimber SJ, Sergouniotis PI
Generation of a human induced pluripotent stem cell line carrying the TYR c.575C>A (p.Ser192Tyr) and c.1205G>A (p.Arg402Gln) variants in homozygous state using CRISPR-Cas9 genome editing
Liu J et al. Generation of a human induced pluripotent stem cell line carrying the TYR c.575C>A (p.Ser192Tyr) and c.1205G>A (p.Arg402Gln) variants in homozygous state using CRISPR-Cas9 genome editing. . 2022-10-00. Pubmed ID: 35933957; DOI: 10.1016/j.scr.2022.102880 WTSIi253-AWTSIi253-A-2 2022-10-00 2022-10-00 PubMed: 35933957 DOI: 10.1016/j.scr.2022.102880Associated cell lines:
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Shan W, Yang H, Ren Q, Wang Q, An G
Generation of TSC1 knockout induced pluripotent stem cell (iPSC) line
Shan W et al. Generation of TSC1 knockout induced pluripotent stem cell (iPSC) line. . 2022-10-00. Pubmed ID: 35961105; DOI: 10.1016/j.scr.2022.102888 BJTTHi001-ABJTTHi001-A-5 2022-10-00 2022-10-00 PubMed: 35961105 DOI: 10.1016/j.scr.2022.102888Associated cell lines:
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Xian X, Liu J, Zhang J, Hao P, Zhai Y, Cheng J, Yue F, Ma M, Zhang Z, Luan F, Ren Q
Generation of an induced pluripotent stem cell lines HMSCASTi002-A from peripheral blood mononuclear cells of a 38-year-old healthy female individual
Xian X et al. Generation of an induced pluripotent stem cell lines HMSCASTi002-A from peripheral blood mononuclear cells of a 38-year-old healthy female individual. . 2022-10-00. Pubmed ID: 36099765; DOI: 10.1016/j.scr.2022.102907 HMSCATi002-A 2022-10-00 2022-10-00 PubMed: 36099765 DOI: 10.1016/j.scr.2022.102907Associated cell lines:
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Sharma V, Nehra S, Singhal N
Generation of AAVS1-EGFP reporter cell lines from an isogenic pair of trisomy 21 and euploid human iPSCs
Sharma V et al. Generation of AAVS1-EGFP reporter cell lines from an isogenic pair of trisomy 21 and euploid human iPSCs. . 2022-10-00. Pubmed ID: 35961104; DOI: 10.1016/j.scr.2022.102890 NSi002-ANSi002-B 2022-10-00 2022-10-00 PubMed: 35961104 DOI: 10.1016/j.scr.2022.102890 -
Zhang Z, Liu J, Zhang J, Xian X, Hao P, Zhai Y, Cheng J, Yue F, Luan F, Ma M, Ren Q
Generation of an induced pluripotent stem cell lines HMSCASTi001-A from peripheral blood mononuclear cells of a 35-year-old healthy male
Zhang Z et al. Generation of an induced pluripotent stem cell lines HMSCASTi001-A from peripheral blood mononuclear cells of a 35-year-old healthy male. . 2022-10-00. Pubmed ID: 36113356; DOI: 10.1016/j.scr.2022.102908 HMSCATi001-A 2022-10-00 2022-10-00 PubMed: 36113356 DOI: 10.1016/j.scr.2022.102908Associated cell lines:
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Ong SLM, Baelde HJ, van IJzendoorn DGP, Bovée JVMG, Szuhai K
Identification of stable housekeeping genes for induced pluripotent stem cells and -derived endothelial cells for drug testing
Ong SLM et al. Identification of stable housekeeping genes for induced pluripotent stem cells and -derived endothelial cells for drug testing. . 2022-09-28. Pubmed ID: 36171445; DOI: 10.1038/s41598-022-20435-w; PMC: PMC9519970 LUMCi001-A 2022-09-28 2022-09-28 PubMed: 36171445 DOI: 10.1038/s41598-022-20435-wAssociated cell lines:
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Duff C, Baruteau J
Modelling urea cycle disorders using iPSCs
Duff C et al. Modelling urea cycle disorders using iPSCs. . 2022-09-26. Pubmed ID: 36163209; DOI: 10.1038/s41536-022-00252-5; PMC: PMC9513077 WAe001-AWAe001-A-13SDQLCHi009-ASDQLCHi036-A 2022-09-26 2022-09-26 PubMed: 36163209 DOI: 10.1038/s41536-022-00252-5Associated cell lines:
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Wang X, Li Z, Qu M, Xiong C, Li H
A homozygous PIWIL2 frameshift variant affects the formation and maintenance of human-induced pluripotent stem cell-derived spermatogonial stem cells and causes Sertoli cell-only syndrome
Wang X et al. A homozygous PIWIL2 frameshift variant affects the formation and maintenance of human-induced pluripotent stem cell-derived spermatogonial stem cells and causes Sertoli cell-only syndrome. . 2022-09-24. Pubmed ID: 36153567; DOI: 10.1186/s13287-022-03175-6; PMC: PMC9509617 HUSTi002-A 2022-09-24 2022-09-24 PubMed: 36153567 DOI: 10.1186/s13287-022-03175-6Associated cell lines:
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Zheng Bixia, Seltzsam Steve, Wang Chunyan, Schierbaum Luca, Schneider Sophia, Wu Chen-Han Wilfred, Dai Rufeng, Connaughton Dervla M, Nakayama Makiko, Mann Nina, Stajic Natasa, Mane Shrikant, Bauer Stuart B, Tasic Velibor, Nam Hyun Joo, Shril Shirlee, Hildebrandt Friedhelm
Whole-exome sequencing identifiesFOXL2,FOXA2andFOXA3as candidate genes for monogenic congenital anomalies of the kidneys and urinary tract
Zheng Bixia et al. Whole-exome sequencing identifiesFOXL2,FOXA2andFOXA3as candidate genes for monogenic congenital anomalies of the kidneys and urinary tract. . 2022-09-22. DOI: 10.1093/ndt/gfab253 QBRIi009-A 2022-09-22 2022-09-22 DOI: 10.1093/ndt/gfab253Associated cell lines:
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Shabaldin Nikita A., Shabaldin Andrei V.
Molecular foundations of the etiology and pathogenesis of Legg-Calve-Perthes disease and prospects for targeted therapy: A literature review
Shabaldin Nikita A. et al. Molecular foundations of the etiology and pathogenesis of Legg-Calve-Perthes disease and prospects for targeted therapy: A literature review. . 2022-09-22. DOI: 10.17816/ptors101679 MCRIi019-AMCRIi019-A-2 2022-09-22 2022-09-22 DOI: 10.17816/ptors101679Associated cell lines:
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Rudraraju R, Gartner MJ, Neil JA, Stout ES, Chen J, Needham EJ, See M, Mackenzie-Kludas C, Yang Lee LY, Wang M, Pointer H, Karavendzas K, Abu-Bonsrah D, Drew D, Sun YBY, Tan JP, Sun G, Salavaty A, Charitakis N, Nim HT, Currie PD, Tham WH, Porrello E, Polo J, Humphrey SJ, Ramialison M, Elliott DA, Subbarao K
Parallel use of pluripotent human stem cell lung and heart models provide new insights for treatment of SARS-CoV-2
Rudraraju R et al. Parallel use of pluripotent human stem cell lung and heart models provide new insights for treatment of SARS-CoV-2. . 2022-09-21. Pubmed ID: 36172136; DOI: 10.1101/2022.09.20.508614; PMC: PMC9516846 MCRIi010-A 2022-09-21 2022-09-21 PubMed: 36172136 DOI: 10.1101/2022.09.20.508614Associated cell lines:
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Jung S, You H, Kim M, Ko G, Lee S, Kang K.
Wnt-activating human skin organoid model of atopic dermatitis induced by Staphylococcus aureus and its protective effects by Cutibacterium acnes
Jung S et al. Wnt-activating human skin organoid model of atopic dermatitis induced by Staphylococcus aureus and its protective effects by Cutibacterium acnes. . 2022-09-16. KSCBi005-A 2022-09-16 2022-09-16Associated cell lines:
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Esser AJ, Mukherjee S, Dereven'kov IA, Makarov SV, Jacobsen DW, Spiekerkoetter U, Hannibal L
Versatile enzymology and heterogeneous phenotypes in cobalamin complementation type C disease
Esser AJ et al. Versatile enzymology and heterogeneous phenotypes in cobalamin complementation type C disease. . 2022-09-16. Pubmed ID: 36105582; DOI: 10.1016/j.isci.2022.104981; PMC: PMC9464900 SDQLCHi021-A 2022-09-16 2022-09-16 PubMed: 36105582 DOI: 10.1016/j.isci.2022.104981Associated cell lines:
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Gao L, Wang F, Wang Y, Hu L, Mao J
A protocol for the generation of patient-specific iPSC lines from peripheral blood mononuclear cells
Gao L et al. A protocol for the generation of patient-specific iPSC lines from peripheral blood mononuclear cells. . 2022-09-16. Pubmed ID: 35834385; DOI: 10.1016/j.xpro.2022.101530; PMC: PMC9287807 NCKDi003-A 2022-09-16 2022-09-16 PubMed: 35834385 DOI: 10.1016/j.xpro.2022.101530Associated cell lines:
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Zink A, Haferkamp U, Wittich A, Beller M, Pless O, Prigione A
High-content screening of mitochondrial polarization in neural cells derived from human pluripotent stem cells
Zink A et al. High-content screening of mitochondrial polarization in neural cells derived from human pluripotent stem cells. . 2022-09-16. Pubmed ID: 35959496; DOI: 10.1016/j.xpro.2022.101602; PMC: PMC9361325 HMGUi001-A 2022-09-16 2022-09-16 PubMed: 35959496 DOI: 10.1016/j.xpro.2022.101602Associated cell lines:
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Ali G, Abdelalim EM
Directed differentiation of human pluripotent stem cells into epidermal keratinocyte-like cells
Ali G et al. Directed differentiation of human pluripotent stem cells into epidermal keratinocyte-like cells. . 2022-09-16. Pubmed ID: 35990735; DOI: 10.1016/j.xpro.2022.101613; PMC: PMC9385691 QBRIi001-AQBRIi002-AQBRIi005-A 2022-09-16 2022-09-16 PubMed: 35990735 DOI: 10.1016/j.xpro.2022.101613Associated cell lines:
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Lickfett S, Menacho C, Zink A, Telugu NS, Beller M, Diecke S, Cambridge S, Prigione A
High-content analysis of neuronal morphology in human iPSC-derived neurons
Lickfett S et al. High-content analysis of neuronal morphology in human iPSC-derived neurons. . 2022-09-16. Pubmed ID: 35990743; DOI: 10.1016/j.xpro.2022.101567; PMC: PMC9386098 BIHi005-ABIHi005-A-24 2022-09-16 2022-09-16 PubMed: 35990743 DOI: 10.1016/j.xpro.2022.101567Associated cell lines:
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Sanjurjo-Soriano C, Erkilic N, Damodar K, Boukhaddaoui H, Diakatou M, Garita-Hernandez M, Mamaeva D, Dubois G, Jazouli Z, Jimenez-Medina C, Goureau O, Meunier I, Kalatzis V
Retinoic acid delays initial photoreceptor differentiation and results in a highly structured mature retinal organoid
Sanjurjo-Soriano C et al. Retinoic acid delays initial photoreceptor differentiation and results in a highly structured mature retinal organoid. . 2022-09-16. Pubmed ID: 36114559; DOI: 10.1186/s13287-022-03146-x; PMC: PMC9482314 INMi001-A 2022-09-16 2022-09-16 PubMed: 36114559 DOI: 10.1186/s13287-022-03146-xAssociated cell lines:
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Seibertz F, Rapedius M, Fakuade FE, Tomsits P, Liutkute A, Cyganek L, Becker N, Majumder R, Clauß S, Fertig N, Voigt N
A modern automated patch-clamp approach for high throughput electrophysiology recordings in native cardiomyocytes
Seibertz F et al. A modern automated patch-clamp approach for high throughput electrophysiology recordings in native cardiomyocytes. . 2022-09-15. Pubmed ID: 36109584; DOI: 10.1038/s42003-022-03871-2; PMC: PMC9477872 UMGi014-C 2022-09-15 2022-09-15 PubMed: 36109584 DOI: 10.1038/s42003-022-03871-2Associated cell lines:
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Yang L, Sun J, Chen Z, Liu L, Sun Y, Lin J, Hu X, Zhao M, Ma Y, Lu D, Li Y, Guo Y, Dong E
The LMNA p.R541C mutation causes dilated cardiomyopathy in human and mice
Yang L et al. The LMNA p.R541C mutation causes dilated cardiomyopathy in human and mice. . 2022-09-15. Pubmed ID: 35714719; DOI: 10.1016/j.ijcard.2022.06.038 USFi003-A 2022-09-15 2022-09-15 PubMed: 35714719 DOI: 10.1016/j.ijcard.2022.06.038Associated cell lines:
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Zlotnik D, Rabinski T, Halfon A, Anzi S, Plaschkes I, Benyamini H, Nevo Y, Gershoni OY, Rosental B, Hershkovitz E, Ben-Zvi A, Vatine GD
P450 oxidoreductase regulates barrier maturation by mediating retinoic acid metabolism in a model of the human BBB
Zlotnik D et al. P450 oxidoreductase regulates barrier maturation by mediating retinoic acid metabolism in a model of the human BBB. . 2022-09-13. Pubmed ID: 35961311; DOI: 10.1016/j.stemcr.2022.07.010; PMC: PMC9481905 BGUi001-ABGUi002-ABGUi003-ABGUi004-ABGUi005-A 2022-09-13 2022-09-13 PubMed: 35961311 DOI: 10.1016/j.stemcr.2022.07.010 -
Sintov E, Nikolskiy I, Barrera V, Hyoje-Ryu Kenty J, Atkin AS, Gerace D, Ho Sui SJ, Boulanger K, Melton DA
Whole-genome CRISPR screening identifies genetic manipulations to reduce immune rejection of stem cell-derived islets
Sintov E et al. Whole-genome CRISPR screening identifies genetic manipulations to reduce immune rejection of stem cell-derived islets. . 2022-09-13. Pubmed ID: 36055241; DOI: 10.1016/j.stemcr.2022.08.002; PMC: PMC9481918 HVRDe008-AHVRDe008-A-1 2022-09-13 2022-09-13 PubMed: 36055241 DOI: 10.1016/j.stemcr.2022.08.002Associated cell lines:
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Pandey S, Jirásko M, Lochman J, Chvátal A, Chottova Dvorakova M, Kučera R
iPSCs in Neurodegenerative Disorders: A Unique Platform for Clinical Research and Personalized Medicine
Pandey S et al. iPSCs in Neurodegenerative Disorders: A Unique Platform for Clinical Research and Personalized Medicine. . 2022-09-10. Pubmed ID: 36143270; DOI: 10.3390/jpm12091485; PMC: PMC9500601 UKBi011-AZZUi007-AIPTi002-ASIAISi004-AFJMUUHi001-AICGi034-A 2022-09-10 2022-09-10 PubMed: 36143270 DOI: 10.3390/jpm12091485Associated cell lines:
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Gómez-Cabello D, Pappas G, Aguilar-Morante D, Dinant C, Bartek J
CtIP-dependent nascent RNA expression flanking DNA breaks guides the choice of DNA repair pathway
Gómez-Cabello D et al. CtIP-dependent nascent RNA expression flanking DNA breaks guides the choice of DNA repair pathway. . 2022-09-09. Pubmed ID: 36085345; DOI: 10.1038/s41467-022-33027-z; PMC: PMC9463442 FRIMOi007-A 2022-09-09 2022-09-09 PubMed: 36085345 DOI: 10.1038/s41467-022-33027-zAssociated cell lines:
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Wunderlich S, Haase A, Merkert S, Jahn K, Deest M, Frieling H, Glage S, Korte W, Martens A, Kirschning A, Zeug A, Ponimaskin E, Göhring G, Ackermann M, Lachmann N, Moritz T, Zweigerdt R, Martin U
Targeted biallelic integration of an inducible Caspase 9 suicide gene in iPSCs for safer therapies
Wunderlich S et al. Targeted biallelic integration of an inducible Caspase 9 suicide gene in iPSCs for safer therapies. . 2022-09-08. Pubmed ID: 35795779; DOI: 10.1016/j.omtm.2022.05.011; PMC: PMC9234009 MHHi001-AMHHi009-A 2022-09-08 2022-09-08 PubMed: 35795779 DOI: 10.1016/j.omtm.2022.05.011 -
Gmach P, Bathe-Peters M, Telugu N, Miller DC, Annibale P
Fluorescence Spectroscopy of Low-Level Endogenous β-Adrenergic Receptor Expression at the Plasma Membrane of Differentiating Human iPSC-Derived Cardiomyocytes
Gmach P et al. Fluorescence Spectroscopy of Low-Level Endogenous β-Adrenergic Receptor Expression at the Plasma Membrane of Differentiating Human iPSC-Derived Cardiomyocytes. . 2022-09-08. Pubmed ID: 36142320; DOI: 10.3390/ijms231810405; PMC: PMC9499492 BIHi005-A 2022-09-08 2022-09-08 PubMed: 36142320 DOI: 10.3390/ijms231810405Associated cell lines:
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Damkham N, Lorthongpanich C, Klaihmon P, Lueangamornnara U, Kheolamai P, Trakarnsanga K, Issaragrisil S
YAP and TAZ play a crucial role in human erythrocyte maturation and enucleation
Damkham N et al. YAP and TAZ play a crucial role in human erythrocyte maturation and enucleation. . 2022-09-08. Pubmed ID: 36076260; DOI: 10.1186/s13287-022-03166-7; PMC: PMC9461202 MUSIi012-AMUSIi012-A-1MUSIi012-A-2 2022-09-08 2022-09-08 PubMed: 36076260 DOI: 10.1186/s13287-022-03166-7Associated cell lines:
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Jagtap S, Potdar C, Yadav R, Pal PK, Datta I
Dopaminergic Neurons Differentiated from LRRK2 I1371V-Induced Pluripotent Stem Cells Display a Lower Yield, α-Synuclein Pathology, and Functional Impairment
Jagtap S et al. Dopaminergic Neurons Differentiated from LRRK2 I1371V-Induced Pluripotent Stem Cells Display a Lower Yield, α-Synuclein Pathology, and Functional Impairment. . 2022-09-07. Pubmed ID: 36006382; DOI: 10.1021/acschemneuro.2c00297 NIMHi001-ANIMHi004-ANIMHi005-ANIMHi006-A 2022-09-07 2022-09-07 PubMed: 36006382 DOI: 10.1021/acschemneuro.2c00297Associated cell lines:
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Zhang YY, Lou Y, Yan H, Tang H
CCNO mutation as a cause of primary ciliary dyskinesia: A case report
Zhang YY et al. CCNO mutation as a cause of primary ciliary dyskinesia: A case report. . 2022-09-06. Pubmed ID: 36157652; DOI: 10.12998/wjcc.v10.i25.9148; PMC: PMC9477031 MHHi016-AMHHi016-B 2022-09-06 2022-09-06 PubMed: 36157652 DOI: 10.12998/wjcc.v10.i25.9148 -
Briso-Montiano Á, Vilas A, Richard E, Ruiz-Sala P, Morato E, Desviat LR, Ugarte M, Rodríguez-Pombo P, Pérez B
Hepatocyte-like cells differentiated from methylmalonic aciduria cblB type induced pluripotent stem cells: A platform for the evaluation of pharmacochaperoning
Briso-Montiano Á et al. Hepatocyte-like cells differentiated from methylmalonic aciduria cblB type induced pluripotent stem cells: A platform for the evaluation of pharmacochaperoning. . 2022-09-01. Pubmed ID: 35569737; DOI: 10.1016/j.bbadis.2022.166433 ESi045-CUAMi002-AUAMi003-A 2022-09-01 2022-09-01 PubMed: 35569737 DOI: 10.1016/j.bbadis.2022.166433 -
Coelho P, Fão L, Mota S, Rego AC
Mitochondrial function and dynamics in neural stem cells and neurogenesis: Implications for neurodegenerative diseases
Coelho P et al. Mitochondrial function and dynamics in neural stem cells and neurogenesis: Implications for neurodegenerative diseases. . 2022-09-00. Pubmed ID: 35714855; DOI: 10.1016/j.arr.2022.101667 HIHCNi002-A 2022-09-00 2022-09-00 PubMed: 35714855 DOI: 10.1016/j.arr.2022.101667Associated cell lines:
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Kwok CK, Sébastien I, Hariharan K, Meiser I, Wihan J, Altmaier S, Karnatz I, Bauer D, Fischer B, Feile A, Cabrera-Socorro A, Rasmussen M, Holst B, Neubauer JC, Clausen C, Verfaillie C, Ebneth A, Hansson M, Steeg R, Zimmermann H
Scalable expansion of iPSC and their derivatives across multiple lineages
Kwok CK et al. Scalable expansion of iPSC and their derivatives across multiple lineages. . 2022-09-00. Pubmed ID: 35595152; DOI: 10.1016/j.reprotox.2022.05.007 UKBi005-ABIONi010-CUKKi018-ABIONi010-C-13BIONi010-C-64 2022-09-00 2022-09-00 PubMed: 35595152 DOI: 10.1016/j.reprotox.2022.05.007Associated cell lines:
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Weiand M, Ballmaier P, Niemietz C, Schmidt H, Zibert A
Combined transgene immortalized urothelial cells capable of reprogramming and hepatic differentiation
Weiand M et al. Combined transgene immortalized urothelial cells capable of reprogramming and hepatic differentiation. . 2022-09-00. Pubmed ID: 35865272; DOI: 10.1016/j.bbrep.2022.101308; PMC: PMC9294256 CHUQi001-A 2022-09-00 2022-09-00 PubMed: 35865272 DOI: 10.1016/j.bbrep.2022.101308Associated cell lines:
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Zeidler M, Kummer KK, Kress M
Towards bridging the translational gap by improved modeling of human nociception in health and disease
Zeidler M et al. Towards bridging the translational gap by improved modeling of human nociception in health and disease. . 2022-09-00. Pubmed ID: 35655042; DOI: 10.1007/s00424-022-02707-6; PMC: PMC9393146 UKWNLi002-ASDUBMSi001-ABGUi006-ABGUi007-A 2022-09-00 2022-09-00 PubMed: 35655042 DOI: 10.1007/s00424-022-02707-6Associated cell lines:
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Huang S, Song J, He C, Cai X, Yuan K, Mei L, Feng Y
Genetic insights, disease mechanisms, and biological therapeutics for Waardenburg syndrome
Huang S et al. Genetic insights, disease mechanisms, and biological therapeutics for Waardenburg syndrome. . 2022-09-00. Pubmed ID: 33633356; DOI: 10.1038/s41434-021-00240-2 JTUi002-ATYWHSTi002-AIMAGINi022-A 2022-09-00 2022-09-00 PubMed: 33633356 DOI: 10.1038/s41434-021-00240-2Associated cell lines:
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Ilieva M, Aldana BI, Vinten KT, Hohmann S, Woofenden TW, Lukjanska R, Waagepetersen HS, Michel TM
Proteomic phenotype of cerebral organoids derived from autism spectrum disorder patients reveal disrupted energy metabolism, cellular components, and biological processes
Ilieva M et al. Proteomic phenotype of cerebral organoids derived from autism spectrum disorder patients reveal disrupted energy metabolism, cellular components, and biological processes. . 2022-09-00. Pubmed ID: 35618886; DOI: 10.1038/s41380-022-01627-2 SDUKIi002-ASDUKIi003-ASDUKIi004-ASDUKIi006-A 2022-09-00 2022-09-00 PubMed: 35618886 DOI: 10.1038/s41380-022-01627-2Associated cell lines:
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Willi L, Abramovich I, Fernandez-Garcia J, Agranovich B, Shulman M, Milman H, Baskin P, Eisen B, Michele DE, Arad M, Binah O, Gottlieb E
Bioenergetic and Metabolic Impairments in Induced Pluripotent Stem Cell-Derived Cardiomyocytes Generated from Duchenne Muscular Dystrophy Patients
Willi L et al. Bioenergetic and Metabolic Impairments in Induced Pluripotent Stem Cell-Derived Cardiomyocytes Generated from Duchenne Muscular Dystrophy Patients. . 2022-08-29. Pubmed ID: 36077200; DOI: 10.3390/ijms23179808; PMC: PMC9456153 IITi001-A 2022-08-29 2022-08-29 PubMed: 36077200 DOI: 10.3390/ijms23179808Associated cell lines:
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Gao H, Yang F, Sattari K, Du X, Fu T, Fu S, Liu X, Lin J, Sun Y, Yao J
Bioinspired two-in-one nanotransistor sensor for the simultaneous measurements of electrical and mechanical cellular responses
Gao H et al. Bioinspired two-in-one nanotransistor sensor for the simultaneous measurements of electrical and mechanical cellular responses. . 2022-08-26. Pubmed ID: 36001656; DOI: 10.1126/sciadv.abn2485; PMC: PMC9401615 WAe009-A 2022-08-26 2022-08-26 PubMed: 36001656 DOI: 10.1126/sciadv.abn2485Associated cell lines:
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Pranty AI, Shumka S, Adjaye J
Bilirubin-Induced Neurological Damage: Current and Emerging iPSC-Derived Brain Organoid Models
Pranty AI et al. Bilirubin-Induced Neurological Damage: Current and Emerging iPSC-Derived Brain Organoid Models. . 2022-08-25. Pubmed ID: 36078055; DOI: 10.3390/cells11172647; PMC: PMC9454749 HHUUKDi005-A 2022-08-25 2022-08-25 PubMed: 36078055 DOI: 10.3390/cells11172647Associated cell lines:
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Kim W, Park E, Yoo HS, Park J, Jung YM, Park JH
Recent Advances in Monitoring Stem Cell Status and Differentiation Using Nano-Biosensing Technologies
Kim W et al. Recent Advances in Monitoring Stem Cell Status and Differentiation Using Nano-Biosensing Technologies. . 2022-08-25. Pubmed ID: 36079970; DOI: 10.3390/nano12172934; PMC: PMC9457759 KSCBi005-AKSCBi005-A-3 2022-08-25 2022-08-25 PubMed: 36079970 DOI: 10.3390/nano12172934Associated cell lines:
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Mahoney-Sanchez L, Bouchaoui H, Boussaad I, Jonneaux A, Timmerman K, Berdeaux O, Ayton S, Krüger R, Duce JA, Devos D, Devedjian JC
Alpha synuclein determines ferroptosis sensitivity in dopaminergic neurons via modulation of ether-phospholipid membrane composition
Mahoney-Sanchez L et al. Alpha synuclein determines ferroptosis sensitivity in dopaminergic neurons via modulation of ether-phospholipid membrane composition. . 2022-08-23. Pubmed ID: 36001957; DOI: 10.1016/j.celrep.2022.111231 HIHDNDi001-AHIHDNDi001-B 2022-08-23 2022-08-23 PubMed: 36001957 DOI: 10.1016/j.celrep.2022.111231Associated cell lines:
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Zink M, Seewald A, Rohrbach M, Brodehl A, Liedtke D, Williams T, Childs SJ, Gerull B
Altered Expression of TMEM43 Causes Abnormal Cardiac Structure and Function in Zebrafish
Zink M et al. Altered Expression of TMEM43 Causes Abnormal Cardiac Structure and Function in Zebrafish. . 2022-08-23. Pubmed ID: 36076925; DOI: 10.3390/ijms23179530; PMC: PMC9455580 HDZi001-A 2022-08-23 2022-08-23 PubMed: 36076925 DOI: 10.3390/ijms23179530Associated cell lines:
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Mouka A, Arkoun B, Moison P, Drévillon L, Jarray R, Brisset S, Mayeur A, Bouligand J, Boland-Auge A, Deleuze JF, Yates F, Lemonnier T, Callier P, Duffourd Y, Nitschke P, Ollivier E, Bourdin A, De Vos J, Livera G, Tachdjian G, Maouche-Chrétien L, Tosca L
iPSCs derived from infertile men carrying complex genetic abnormalities can generate primordial germ-like cells
Mouka A et al. iPSCs derived from infertile men carrying complex genetic abnormalities can generate primordial germ-like cells. . 2022-08-22. Pubmed ID: 35995809; DOI: 10.1038/s41598-022-17337-2; PMC: PMC9395518 UHOMi002-A 2022-08-22 2022-08-22 PubMed: 35995809 DOI: 10.1038/s41598-022-17337-2Associated cell lines:
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Miguel-Escalada I, Maestro MÁ, Balboa D, Elek A, Bernal A, Bernardo E, Grau V, García-Hurtado J, Sebé-Pedrós A, Ferrer J
Pancreas agenesis mutations disrupt a lead enhancer controlling a developmental enhancer cluster
Miguel-Escalada I et al. Pancreas agenesis mutations disrupt a lead enhancer controlling a developmental enhancer cluster. . 2022-08-22. Pubmed ID: 35998583; DOI: 10.1016/j.devcel.2022.07.014; PMC: PMC9426562 WAe001-A 2022-08-22 2022-08-22 PubMed: 35998583 DOI: 10.1016/j.devcel.2022.07.014Associated cell lines:
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Memon B, Elsayed AK, Bettahi I, Suleiman N, Younis I, Wehedy E, Abou-Samra AB, Abdelalim EM
iPSCs derived from insulin resistant offspring of type 2 diabetic patients show increased oxidative stress and lactate secretion
Memon B et al. iPSCs derived from insulin resistant offspring of type 2 diabetic patients show increased oxidative stress and lactate secretion. . 2022-08-20. Pubmed ID: 35987697; DOI: 10.1186/s13287-022-03123-4; PMC: PMC9392338 QBRIi007-AQBRIi009-A 2022-08-20 2022-08-20 PubMed: 35987697 DOI: 10.1186/s13287-022-03123-4Associated cell lines:
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Sánchez-Tejerina D, Restrepo-Vera JL, Rovira-Moreno E, Codina-Sola M, Llauradó A, Sotoca J, Salvado M, Raguer N, García-Arumí E, Juntas-Morales R
An Atypical Presentation of Upper Motor Neuron Predominant Juvenile Amyotrophic Lateral Sclerosis Associated with TARDBP Gene: A Case Report and Review of the Literature
Sánchez-Tejerina D et al. An Atypical Presentation of Upper Motor Neuron Predominant Juvenile Amyotrophic Lateral Sclerosis Associated with TARDBP Gene: A Case Report and Review of the Literature. . 2022-08-19. Pubmed ID: 36011394; DOI: 10.3390/genes13081483; PMC: PMC9407925 KEIOi001-A 2022-08-19 2022-08-19 PubMed: 36011394 DOI: 10.3390/genes13081483Associated cell lines:
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Pearson G, Song C, Hohmann S, Prokhorova T, Sheldrick-Michel TM, Knöpfel T
DNA Methylation Profiles of GAD1 in Human Cerebral Organoids of Autism Indicate Disrupted Epigenetic Regulation during Early Development
Pearson G et al. DNA Methylation Profiles of GAD1 in Human Cerebral Organoids of Autism Indicate Disrupted Epigenetic Regulation during Early Development. . 2022-08-16. Pubmed ID: 36012452; DOI: 10.3390/ijms23169188; PMC: PMC9408997 SDUKIi002-ASDUKIi003-ASDUKIi004-ASDUKIi006-A 2022-08-16 2022-08-16 PubMed: 36012452 DOI: 10.3390/ijms23169188Associated cell lines:
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Ghasemzad M, Hashemi M, Lavasani ZM, Hossein-Khannazer N, Bakhshandeh H, Gramignoli R, Keshavarz Alikhani H, Najimi M, Nikeghbalian S, Vosough M
Novel Gene-Correction-Based Therapeutic Modalities for Monogenic Liver Disorders
Ghasemzad M et al. Novel Gene-Correction-Based Therapeutic Modalities for Monogenic Liver Disorders. . 2022-08-15. Pubmed ID: 36004917; DOI: 10.3390/bioengineering9080392; PMC: PMC9404740 SMBCi004-ASDQLCHi036-A 2022-08-15 2022-08-15 PubMed: 36004917 DOI: 10.3390/bioengineering9080392Associated cell lines:
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Liang Y, Tan F, Sun X, Cui Z, Gu J, Mao S, Chan HF, Tang S, Chen J
Aberrant Retinal Pigment Epithelial Cells Derived from Induced Pluripotent Stem Cells of a Retinitis Pigmentosa Patient with the PRPF6 Mutation
Liang Y et al. Aberrant Retinal Pigment Epithelial Cells Derived from Induced Pluripotent Stem Cells of a Retinitis Pigmentosa Patient with the PRPF6 Mutation. . 2022-08-12. Pubmed ID: 36012314; DOI: 10.3390/ijms23169049; PMC: PMC9409096 CSUASOi004-A 2022-08-12 2022-08-12 PubMed: 36012314 DOI: 10.3390/ijms23169049Associated cell lines:
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Loos Malte, Klampe Birgit, Schulze Thomas, Yin Xiaoke, Theofilatos Konstantinos, Ulmer Bärbel, Schulz Carl, Behrens Charlotta, Bergen Tessa Van, Adami Eleonora, Maatz Henrike, Schweizer Michaela, Brodesser Susanne, Skryabin Boris, Rozhdestvensky Timofey, Bodbin Sara, Christ Torsten, Denning Chris, Huebner Norbert, Mayr Manuel, Eschenhagen Thomas, Hansen Arne
Human model of primary carnitine deficiency cardiomyopathy reveals ferroptosis as a novel disease mechanism
Loos Malte et al. Human model of primary carnitine deficiency cardiomyopathy reveals ferroptosis as a novel disease mechanism. . 2022-08-11. DOI: 10.21203/rs.3.rs-1880728/v1 UKEi001-A 2022-08-11 2022-08-11 DOI: 10.21203/rs.3.rs-1880728/v1Associated cell lines:
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Li W, Xing C, Bao L, Han S, Luo T, Wang Z, Fan H
Comprehensive analysis of RNA m6A methylation in pressure overload-induced cardiac hypertrophy
Li W et al. Comprehensive analysis of RNA m6A methylation in pressure overload-induced cardiac hypertrophy. . 2022-08-11. Pubmed ID: 35953789; DOI: 10.1186/s12864-022-08833-w; PMC: PMC9373449 ZZUNEUi023-A 2022-08-11 2022-08-11 PubMed: 35953789 DOI: 10.1186/s12864-022-08833-wAssociated cell lines:
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Wang F, Han Y, Sang W, Wang L, Liang X, Wang L, Xing Q, Guo Y, Zhang J, Zhang L, Zukela T, Xiaokereti J, Lu Y, Zhou X, Tang B, Li Y
In Vitro Drug Screening Using iPSC-Derived Cardiomyocytes of a Long QT-Syndrome Patient Carrying KCNQ1 & TRPM4 Dual Mutation: An Experimental Personalized Treatment
Wang F et al. In Vitro Drug Screening Using iPSC-Derived Cardiomyocytes of a Long QT-Syndrome Patient Carrying KCNQ1 & TRPM4 Dual Mutation: An Experimental Personalized Treatment. . 2022-08-11. Pubmed ID: 36010573; DOI: 10.3390/cells11162495; PMC: PMC9406448 FAHXMUi001-A 2022-08-11 2022-08-11 PubMed: 36010573 DOI: 10.3390/cells11162495Associated cell lines:
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Pitstick AL, Poling HM, Sundaram N, Lewis PL, Kechele DO, Sanchez JG, Scott MA, Broda TR, Helmrath MA, Wells JM, Mayhew CN
Aggregation of cryopreserved mid-hindgut endoderm for more reliable and reproducible hPSC-derived small intestinal organoid generation
Pitstick AL et al. Aggregation of cryopreserved mid-hindgut endoderm for more reliable and reproducible hPSC-derived small intestinal organoid generation. . 2022-08-09. Pubmed ID: 35905739; DOI: 10.1016/j.stemcr.2022.06.011; PMC: PMC9391520 CCHMCi001-ACCHMCi002-ACUSTOMi001-A 2022-08-09 2022-08-09 PubMed: 35905739 DOI: 10.1016/j.stemcr.2022.06.011Associated cell lines:
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Ahmed E, Fieldes M, Bourguignon C, Mianné J, Petit A, Jory M, Cazevieille C, Boukhaddaoui H, Garnett JP, Hirtz C, Massiera G, Vachier I, Assou S, Bourdin A, De Vos J
Differentiation of Human Induced Pluripotent Stem Cells from Patients with Severe COPD into Functional Airway Epithelium
Ahmed E et al. Differentiation of Human Induced Pluripotent Stem Cells from Patients with Severe COPD into Functional Airway Epithelium. . 2022-08-05. Pubmed ID: 35954266; DOI: 10.3390/cells11152422; PMC: PMC9368529 UHOMi001-AUHOMi002-AUHOMi003-AUHOMi004-AUHOMi005-A 2022-08-05 2022-08-05 PubMed: 35954266 DOI: 10.3390/cells11152422Associated cell lines:
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Rothammer N, Woo MS, Bauer S, Binkle-Ladisch L, Di Liberto G, Egervari K, Wagner I, Haferkamp U, Pless O, Merkler D, Engler JB, Friese MA
G9a dictates neuronal vulnerability to inflammatory stress via transcriptional control of ferroptosis
Rothammer N et al. G9a dictates neuronal vulnerability to inflammatory stress via transcriptional control of ferroptosis. . 2022-08-05. Pubmed ID: 35930635; DOI: 10.1126/sciadv.abm5500; PMC: PMC9355351 ZIPi013-B 2022-08-05 2022-08-05 PubMed: 35930635 DOI: 10.1126/sciadv.abm5500Associated cell lines:
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Birke R, Ast J, Roosen DA, Lee J, Roßmann K, Huhn C, Mathes B, Lisurek M, Bushiri D, Sun H, Jones B, Lehmann M, Levitz J, Haucke V, Hodson DJ, Broichhagen J
Sulfonated red and far-red rhodamines to visualize SNAP- and Halo-tagged cell surface proteins
Birke R et al. Sulfonated red and far-red rhodamines to visualize SNAP- and Halo-tagged cell surface proteins. . 2022-08-03. Pubmed ID: 35188523; DOI: 10.1039/d1ob02216d; PMC: PMC9346974 BIHi005-A 2022-08-03 2022-08-03 PubMed: 35188523 DOI: 10.1039/d1ob02216dAssociated cell lines:
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Adelipour M, Saleth LR, Ghavami S, Alagarsamy KN, Dhingra S, Allameh A
The role of autophagy in the metabolism and differentiation of stem cells
Adelipour M et al. The role of autophagy in the metabolism and differentiation of stem cells. . 2022-08-01. Pubmed ID: 35447339; DOI: 10.1016/j.bbadis.2022.166412 UOMi005-AUOMi006-A 2022-08-01 2022-08-01 PubMed: 35447339 DOI: 10.1016/j.bbadis.2022.166412 -
Ura H, Togi S, Hatanaka H, Niida Y
Establishment of a human induced pluripotent stem cell line, KMUGMCi004-A, from a patient bearing a heterozygous c.1832delG mutation in the APC gene leading familial adenomatous polyposis (FAP)
Ura H et al. Establishment of a human induced pluripotent stem cell line, KMUGMCi004-A, from a patient bearing a heterozygous c.1832delG mutation in the APC gene leading familial adenomatous polyposis (FAP). . 2022-08-00. Pubmed ID: 35868288; DOI: 10.1016/j.scr.2022.102867 KMUGMCi004-A 2022-08-00 2022-08-00 PubMed: 35868288 DOI: 10.1016/j.scr.2022.102867Associated cell lines:
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Becklin KL, Draper GM, Madden RA, Kluesner MG, Koga T, Huang M, Weiss WA, Spector LG, Largaespada DA, Moriarity BS, Webber BR
Developing Bottom-Up Induced Pluripotent Stem Cell Derived Solid Tumor Models Using Precision Genome Editing Technologies
Becklin KL et al. Developing Bottom-Up Induced Pluripotent Stem Cell Derived Solid Tumor Models Using Precision Genome Editing Technologies. . 2022-08-00. Pubmed ID: 35972367; DOI: 10.1089/crispr.2022.0032; PMC: PMC9529369 CHOPi001-A 2022-08-00 2022-08-00 PubMed: 35972367 DOI: 10.1089/crispr.2022.0032Associated cell lines:
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Ura H, Togi S, Iwata Y, Ozaki M, Niida Y
Establishment of a human induced pluripotent stem cell line, KMUGMCi002-A, from a patient bearing a heterozygous c.6362_6364del mutation in the NIPBL gene leading Cornelia de Lange syndrome (CdLS)
Ura H et al. Establishment of a human induced pluripotent stem cell line, KMUGMCi002-A, from a patient bearing a heterozygous c.6362_6364del mutation in the NIPBL gene leading Cornelia de Lange syndrome (CdLS). . 2022-08-00. Pubmed ID: 35834947; DOI: 10.1016/j.scr.2022.102860 KMUGMCi002-A 2022-08-00 2022-08-00 PubMed: 35834947 DOI: 10.1016/j.scr.2022.102860Associated cell lines:
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Srivastava A, Jaryal R, Rockman-Greenberg C, Dhingra S
Establishment of a new human iPSC cell line (UOMi007-A) from a patient with Hypophosphatasia
Srivastava A et al. Establishment of a new human iPSC cell line (UOMi007-A) from a patient with Hypophosphatasia. . 2022-08-00. Pubmed ID: 35700635; DOI: 10.1016/j.scr.2022.102839 UOMi005-AUOMi006-AUOMi007-A 2022-08-00 2022-08-00 PubMed: 35700635 DOI: 10.1016/j.scr.2022.102839 -
Zhang A, Lu J, Xiao F
An induced pluripotent stem cell line (FHUSTCi002-A) derived from a patient with leucoencephalopathy with brain stem and spinal cord involvement and lactate elevation
Zhang A et al. An induced pluripotent stem cell line (FHUSTCi002-A) derived from a patient with leucoencephalopathy with brain stem and spinal cord involvement and lactate elevation. . 2022-08-00. Pubmed ID: 35914483; DOI: 10.1016/j.scr.2022.102872 FHUSTCi002-A 2022-08-00 2022-08-00 PubMed: 35914483 DOI: 10.1016/j.scr.2022.102872Associated cell lines:
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Ou-Yang CH, Lin HI, Lin CH
Generation of a human induced pluripotent stem cell line NTUHi002-A from a patient with aceruloplasminemia harboring a homozygous splicing mutation c.607+1 delG in CP gene
Ou-Yang CH et al. Generation of a human induced pluripotent stem cell line NTUHi002-A from a patient with aceruloplasminemia harboring a homozygous splicing mutation c.607+1 delG in CP gene. . 2022-08-00. Pubmed ID: 35868289; DOI: 10.1016/j.scr.2022.102856 NTUHi002-A 2022-08-00 2022-08-00 PubMed: 35868289 DOI: 10.1016/j.scr.2022.102856Associated cell lines:
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Sun R, Liu Q, Mu L, Wang A, Zhao J, Long Y, Liu L
A familiar cerebral cavernous malformations (FCCMs) patient with CCM1 deletion-frameshift mutation generates an induced pluripotent stem cell line (NFHHMUi001-A)
Sun R et al. A familiar cerebral cavernous malformations (FCCMs) patient with CCM1 deletion-frameshift mutation generates an induced pluripotent stem cell line (NFHHMUi001-A). . 2022-08-00. Pubmed ID: 35716468; DOI: 10.1016/j.scr.2022.102838 NFHHMUi001-A 2022-08-00 2022-08-00 PubMed: 35716468 DOI: 10.1016/j.scr.2022.102838Associated cell lines:
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Min L, Yin Y, Zhao Q, Wang S
Establishment of a human iPSC line (SUTCMi001-A) derived from a healthy donor
Min L et al. Establishment of a human iPSC line (SUTCMi001-A) derived from a healthy donor. . 2022-08-00. Pubmed ID: 35843020; DOI: 10.1016/j.scr.2022.102849 SUTCMi001-A 2022-08-00 2022-08-00 PubMed: 35843020 DOI: 10.1016/j.scr.2022.102849Associated cell lines:
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Calamaio S, Serzanti M, Morlino S, Massardi M, Ritelli M, Piovani G, Colombi M, Cortellini V, Castori M, Dell'Era P, Micale L
Generation of the induced pluripotent stem cell line UNIBSi017-A from an individual with cardiospondylocarpofacial syndrome and the MAP3K7 c.737-7A > G variant
Calamaio S et al. Generation of the induced pluripotent stem cell line UNIBSi017-A from an individual with cardiospondylocarpofacial syndrome and the MAP3K7 c.737-7A > G variant. . 2022-08-00. Pubmed ID: 35700636; DOI: 10.1016/j.scr.2022.102837 UNIBSi017-A 2022-08-00 2022-08-00 PubMed: 35700636 DOI: 10.1016/j.scr.2022.102837Associated cell lines:
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Strnadel J, Dumortier HM, Hajduchova D, Zahumenska R, Nosal V, Smolar M, Marcinek J, Kalman M, Mersakova S, Brany D, Juhas S, Juhasova J, Studenovska H, Mitruskova B, Suroviakova S, Novakova S, Skovierova H, Kurca E, Pecova R, Plank L, Halasova E
In vitro modeling of amyotrophic lateral sclerosis with induced pluripotent stem cell technology-derived cell line ORIONi002-A
Strnadel J et al. In vitro modeling of amyotrophic lateral sclerosis with induced pluripotent stem cell technology-derived cell line ORIONi002-A. . 2022-08-00. Pubmed ID: 35907349; DOI: 10.1016/j.scr.2022.102870 ORIONi002-A 2022-08-00 2022-08-00 PubMed: 35907349 DOI: 10.1016/j.scr.2022.102870Associated cell lines:
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Cui Y, Huang W, Du F, Yin X, Feng L, Li B
Therapeutic benefits of niraparib tosylate as radio sensitizer in esophageal squamous cell carcinoma: an in vivo and in vitro preclinical study
Cui Y et al. Therapeutic benefits of niraparib tosylate as radio sensitizer in esophageal squamous cell carcinoma: an in vivo and in vitro preclinical study. . 2022-08-00. Pubmed ID: 35364771; DOI: 10.1007/s12094-022-02818-7; PMC: PMC9283188 CSUASOi008-A 2022-08-00 2022-08-00 PubMed: 35364771 DOI: 10.1007/s12094-022-02818-7Associated cell lines:
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Gao X, Li R, Yourick JJ, Sprando RL
A transcriptomic dataset comparing two methods of hepatocyte differentiation from human induced pluripotent stem cells
Gao X et al. A transcriptomic dataset comparing two methods of hepatocyte differentiation from human induced pluripotent stem cells. . 2022-08-00. Pubmed ID: 35898856; DOI: 10.1016/j.dib.2022.108477; PMC: PMC9309642 OARSAi002-A 2022-08-00 2022-08-00 PubMed: 35898856 DOI: 10.1016/j.dib.2022.108477Associated cell lines:
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Cheng D, Zhang S, Li X, Wang L, Dong J, Sang H
An integration-free iPSC line ZZUNEUi028-A derived from a patient with hypertrophic cardiomyopathy carrying a heterozygous mutation (c. 1504 C > T) in MYBPC3 gene
Cheng D et al. An integration-free iPSC line ZZUNEUi028-A derived from a patient with hypertrophic cardiomyopathy carrying a heterozygous mutation (c. 1504 C > T) in MYBPC3 gene. . 2022-08-00. Pubmed ID: 35772297; DOI: 10.1016/j.scr.2022.102848 ZZUNEUi028-A 2022-08-00 2022-08-00 PubMed: 35772297 DOI: 10.1016/j.scr.2022.102848Associated cell lines:
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Grigor'eva EV, Malakhova AA, Sorogina DA, Pavlova SV, Malankhanova TB, Abramycheva NY, Klyushnikov SA, Illarioshkin SN, Zakian SM
Generation of induced pluripotent stem cell line, ICGi033-A, by reprogramming peripheral blood mononuclear cells from a patient with Huntington's disease
Grigor'eva EV et al. Generation of induced pluripotent stem cell line, ICGi033-A, by reprogramming peripheral blood mononuclear cells from a patient with Huntington's disease. . 2022-08-00. Pubmed ID: 35872525; DOI: 10.1016/j.scr.2022.102868 ICGi033-A 2022-08-00 2022-08-00 PubMed: 35872525 DOI: 10.1016/j.scr.2022.102868Associated cell lines:
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Mitchell MW, Grandizio C, Turan N, Requesens DV
An induced pluripotent stem cell line (CIMRi001-A) from a Vici syndrome donor with a homozygous recessive c.1007A>G (p.Q336R) mutation in the EPG5 gene
Mitchell MW et al. An induced pluripotent stem cell line (CIMRi001-A) from a Vici syndrome donor with a homozygous recessive c.1007A>G (p.Q336R) mutation in the EPG5 gene. . 2022-08-00. Pubmed ID: 35700637; DOI: 10.1016/j.scr.2022.102833; PMC: PMC9375524 CIMRi001-A 2022-08-00 2022-08-00 PubMed: 35700637 DOI: 10.1016/j.scr.2022.102833Associated cell lines:
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Sun Y, Fu J, Yang J, Zhao J, Rong J
Generation of a RRAGA knockout human iPSC line GIBHi002-A-5 using CRISPR/Cas9 technology
Sun Y et al. Generation of a RRAGA knockout human iPSC line GIBHi002-A-5 using CRISPR/Cas9 technology. . 2022-08-00. Pubmed ID: 35870248; DOI: 10.1016/j.scr.2022.102859 GIBHi002-AGIBHi002-A-5 2022-08-00 2022-08-00 PubMed: 35870248 DOI: 10.1016/j.scr.2022.102859Associated cell lines:
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Ding Y, Carvalho E, Murphy C, McInerney V, Krawczyk J, O'Brien T, Howard L, Cai L, Shen S
Corrigendum to "Derivation of familial iPSC lines from three patients with retinitis pigmentosa carrying an autosomal dominant RPE65 mutation (NUIGi027-A, NUIGi028-A, NUIGi029-A)" [Stem Cell Res. (43) 2020 101665]
Ding Y et al. Corrigendum to "Derivation of familial iPSC lines from three patients with retinitis pigmentosa carrying an autosomal dominant RPE65 mutation (NUIGi027-A, NUIGi028-A, NUIGi029-A)" [Stem Cell Res. (43) 2020 101665]. . 2022-08-00. Pubmed ID: 35772298; DOI: 10.1016/j.scr.2022.102850 NUIGi027-ANUIGi028-ANUIGi029-A 2022-08-00 2022-08-00 PubMed: 35772298 DOI: 10.1016/j.scr.2022.102850Associated cell lines:
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Fan X, Cyganek L, Nitschke K, Uhlig S, Nuhn P, Bieback K, Duerschmied D, El-Battrawy I, Zhou X, Akin I
Functional Characterization of Human Induced Pluripotent Stem Cell-Derived Endothelial Cells
Fan X et al. Functional Characterization of Human Induced Pluripotent Stem Cell-Derived Endothelial Cells. . 2022-07-31. Pubmed ID: 35955642; DOI: 10.3390/ijms23158507; PMC: PMC9368986 UMGi124-AUMGi014-BUMGi130-A 2022-07-31 2022-07-31 PubMed: 35955642 DOI: 10.3390/ijms23158507 -
Caudal A, Mondejar-Parreño G, Vera CD, Williams DR, Shenoy SP, Liang D, Wu JC
Generation of human induced pluripotent stem cell lines carrying heterozygous PLN mutation from dilated cardiomyopathy patients
Caudal A et al. Generation of human induced pluripotent stem cell lines carrying heterozygous PLN mutation from dilated cardiomyopathy patients. . 2022-08-00. Pubmed ID: 35853412; DOI: 10.1016/j.scr.2022.102855; PMC: PMC9681708 SCVIi001-ASCVIi002-ASCVIi049-ASCVIi050-A 2022-08-00 2022-08-00 PubMed: 35853412 DOI: 10.1016/j.scr.2022.102855Associated cell lines:
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Azzam SK, Alsafar H, Sajini AA
Generation of the UAE's first Emirati induced pluripotent stem cell line KUSTi001-A from peripheral blood derived CD34+ hematopoietic cells
Azzam SK et al. Generation of the UAE's first Emirati induced pluripotent stem cell line KUSTi001-A from peripheral blood derived CD34+ hematopoietic cells. . 2022-08-00. Pubmed ID: 35816920; DOI: 10.1016/j.scr.2022.102853 UOMi002-AKUSTi001-A 2022-08-00 2022-08-00 PubMed: 35816920 DOI: 10.1016/j.scr.2022.102853Associated cell lines:
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Casamassa A, Zanetti A, Ferrari D, Lombardi I, Galluzzi G, D'Avanzo F, Cipressa G, Bertozzi A, Torrente I, Vescovi AL, Tomanin R, Rosati J
Generation of an induced pluripotent stem cells line, CSSi014-A 9407, carrying the variant c.479C>T in the human iduronate 2-sulfatase (hIDS) gene
Casamassa A et al. Generation of an induced pluripotent stem cells line, CSSi014-A 9407, carrying the variant c.479C>T in the human iduronate 2-sulfatase (hIDS) gene. . 2022-08-00. Pubmed ID: 35759972; DOI: 10.1016/j.scr.2022.102846 CSSi011-ACSSi014-A 2022-08-00 2022-08-00 PubMed: 35759972 DOI: 10.1016/j.scr.2022.102846 -
Vera CD, Manhas A, Shenoy SP, Wheeler MT, Sallam K, Wu JC
Generation of two induced pluripotent stem cell lines carrying the phospholamban R14del mutation for modeling ARVD/C
Vera CD et al. Generation of two induced pluripotent stem cell lines carrying the phospholamban R14del mutation for modeling ARVD/C. . 2022-08-00. Pubmed ID: 35700631; DOI: 10.1016/j.scr.2022.102834; PMC: PMC9476586 SCVIi030-ASCVIi031-A 2022-08-00 2022-08-00 PubMed: 35700631 DOI: 10.1016/j.scr.2022.102834Associated cell lines:
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Hall JC, Paull D, Pébay A, Lidgerwood GE
Human pluripotent stem cells for the modelling of retinal pigment epithelium homeostasis and disease: A review
Hall JC et al. Human pluripotent stem cells for the modelling of retinal pigment epithelium homeostasis and disease: A review. . 2022-08-00. Pubmed ID: 35739648; DOI: 10.1111/ceo.14128; PMC: PMC9546239 FRIMOi003-AFRIMOi004-A 2022-08-00 2022-08-00 PubMed: 35739648 DOI: 10.1111/ceo.14128Associated cell lines:
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Kang JY, Mun D, Chun Y, Kim H, Yun N, Lee SH, Joung B
Generation of a heterozygous TPM1-E192K knock-in human induced pluripotent stem cell line using CRISPR/Cas9 system
Kang JY et al. Generation of a heterozygous TPM1-E192K knock-in human induced pluripotent stem cell line using CRISPR/Cas9 system. . 2022-08-00. Pubmed ID: 35917600; DOI: 10.1016/j.scr.2022.102878 KSCBi018-AKSCBi018-A-1 2022-08-00 2022-08-00 PubMed: 35917600 DOI: 10.1016/j.scr.2022.102878Associated cell lines:
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Zhao J, Wang L, Zhu K, Chen X, Qin F, Li X, Dong J, Tao H
Human induced pluripotent stem cell line ZZUNEUi027-A generated from a long QT syndrome patient with a heterozygous KCNH2 (c. 128 A > G) mutant
Zhao J et al. Human induced pluripotent stem cell line ZZUNEUi027-A generated from a long QT syndrome patient with a heterozygous KCNH2 (c. 128 A > G) mutant. . 2022-08-00. Pubmed ID: 35700634; DOI: 10.1016/j.scr.2022.102836 ZZUNEUi027-A 2022-08-00 2022-08-00 PubMed: 35700634 DOI: 10.1016/j.scr.2022.102836Associated cell lines:
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Han Z, Wang J, Luan J, Cui Y, Han J
Development of a human iPSC line (SMBCi017-A) from a healthy donor
Han Z et al. Development of a human iPSC line (SMBCi017-A) from a healthy donor. . 2022-08-00. Pubmed ID: 35872524; DOI: 10.1016/j.scr.2022.102852 IMAGINi004-AIMAGINi005-ASMBCi017-A 2022-08-00 2022-08-00 PubMed: 35872524 DOI: 10.1016/j.scr.2022.102852Associated cell lines:
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Ni P, Zhou C, Meng Y, Xue R, Yang X, Li L, Zhao L, Wei J, Ni R, Wang Y, Ma X, Guo W, Wang Q, Li T
Generation and characterization of human-derived iPSC lines from two cousins with schizophrenia and bipolar disorder and their unaffected cousin
Ni P et al. Generation and characterization of human-derived iPSC lines from two cousins with schizophrenia and bipolar disorder and their unaffected cousin. . 2022-08-00. Pubmed ID: 35700633; DOI: 10.1016/j.scr.2022.102832 WCHi004-AWCHi005-AWCHi006-A 2022-08-00 2022-08-00 PubMed: 35700633 DOI: 10.1016/j.scr.2022.102832 -
Efendic F, Völkner C, Krohn S, Murua Escobar H, Venkateswaran S, Bennett S, Hermann A, Frech MJ
Generation of the human iPSC line AKOSi010-A from fibroblasts of a female FAHN patient, carrying the compound heterozygous mutation p.Gly45Arg/p.His319Arg
Efendic F et al. Generation of the human iPSC line AKOSi010-A from fibroblasts of a female FAHN patient, carrying the compound heterozygous mutation p.Gly45Arg/p.His319Arg. . 2022-08-00. Pubmed ID: 35843022; DOI: 10.1016/j.scr.2022.102863 AKOSi006-AAKOSi007-AAKOSi010-A 2022-08-00 2022-08-00 PubMed: 35843022 DOI: 10.1016/j.scr.2022.102863Associated cell lines:
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Li J, Fan Y, Fan L, Liu F, Hao X, Li M, Mao C, Xu Y, Shi C
Generation of an induced pluripotent stem cell line (ZZUi036-A) derived from skin fibroblasts of a Neuronal intranuclear inclusion disease patient with GGC repeat expansion in the NOTCH2NLC gene
Li J et al. Generation of an induced pluripotent stem cell line (ZZUi036-A) derived from skin fibroblasts of a Neuronal intranuclear inclusion disease patient with GGC repeat expansion in the NOTCH2NLC gene. . 2022-08-00. Pubmed ID: 35772299; DOI: 10.1016/j.scr.2022.102844 ZZUi036-A 2022-08-00 2022-08-00 PubMed: 35772299 DOI: 10.1016/j.scr.2022.102844Associated cell lines:
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Zheng W, Zhong Y, Yuan L, Yu X, Wang X, Yang C, Liu H, Lv P, Luo Y, Qiu B, Liu J, Yang B
Generation of a human embryonic stem cell line (SMUDHe010-A-82) carrying a homozygous c.1538G > A (p.G513D) mutation in the OSMR gene by CRISPR/Cas9-mediated homologous recombination
Zheng W et al. Generation of a human embryonic stem cell line (SMUDHe010-A-82) carrying a homozygous c.1538G > A (p.G513D) mutation in the OSMR gene by CRISPR/Cas9-mediated homologous recombination. . 2022-08-00. Pubmed ID: 35714449; DOI: 10.1016/j.scr.2022.102842 WAe009-A-82 2022-08-00 2022-08-00 PubMed: 35714449 DOI: 10.1016/j.scr.2022.102842Associated cell lines:
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Jiang X, Hu R, Li C, Xu X, Zhou P, Cao Y, Wang J, Wei Z
Generation of an induced pluripotent stem cell line AMUFAHi002-A from polycystic ovary syndrome patient
Jiang X et al. Generation of an induced pluripotent stem cell line AMUFAHi002-A from polycystic ovary syndrome patient. . 2022-08-00. Pubmed ID: 35914484; DOI: 10.1016/j.scr.2022.102875 AMUFAHi002-A 2022-08-00 2022-08-00 PubMed: 35914484 DOI: 10.1016/j.scr.2022.102875Associated cell lines:
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Ding Y, Chen H, Zhao J, Wang Y, Deng Y
Establishment of SIAISi021-A, an induced pluripotent stem cell (iPSC) line from a 71-year-old Chinese Han male with Alzheimer's Disease (AD) having two copies of APOE4/4 allele
Ding Y et al. Establishment of SIAISi021-A, an induced pluripotent stem cell (iPSC) line from a 71-year-old Chinese Han male with Alzheimer's Disease (AD) having two copies of APOE4/4 allele. . 2022-08-00. Pubmed ID: 35843023; DOI: 10.1016/j.scr.2022.102866 SIAISi021-A 2022-08-00 2022-08-00 PubMed: 35843023 DOI: 10.1016/j.scr.2022.102866Associated cell lines:
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Vaziri N, Marques D, Wang X, Machiraju P, Narang A, Vlahos K, Pantelis C, Greenway SC, Bousman CA
Generation of two human induced pluripotent stem cell lines from peripheral blood mononuclear cells of clozapine-tolerant and clozapine-induced myocarditis patients with treatment-resistant schizophrenia
Vaziri N et al. Generation of two human induced pluripotent stem cell lines from peripheral blood mononuclear cells of clozapine-tolerant and clozapine-induced myocarditis patients with treatment-resistant schizophrenia. . 2022-08-00. Pubmed ID: 35917601; DOI: 10.1016/j.scr.2022.102877 UOCi001-AUOCi002-A 2022-08-00 2022-08-00 PubMed: 35917601 DOI: 10.1016/j.scr.2022.102877 -
Kondrateva E, Panchuk I, Demchenko A, Grigorieva O, Zheglo D, Voronina E, Erofeeva A, Tabakov V, Orlova M, Lavrov A, Smirnikhina S, Kutsev S
Generation of induced pluripotent stem cell line (RCMGi008-A) from human skin fibroblasts of a cystic fibrosis patient with compound heterozygous F508del/CFTRdele2.3 mutations in CFTR gene
Kondrateva E et al. Generation of induced pluripotent stem cell line (RCMGi008-A) from human skin fibroblasts of a cystic fibrosis patient with compound heterozygous F508del/CFTRdele2.3 mutations in CFTR gene. . 2022-08-00. Pubmed ID: 35843019; DOI: 10.1016/j.scr.2022.102854 RCMGi008-A 2022-08-00 2022-08-00 PubMed: 35843019 DOI: 10.1016/j.scr.2022.102854Associated cell lines:
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Im YS, Yoo DH, Kim HE, Oh JY, Kim YO
Generation of integration-free induced pluripotent stem cell line (KSCBi012-A) from urinary epithelial cells of a healthy male individual
Im YS et al. Generation of integration-free induced pluripotent stem cell line (KSCBi012-A) from urinary epithelial cells of a healthy male individual. . 2022-08-00. Pubmed ID: 35700632; DOI: 10.1016/j.scr.2022.102841 KSCBi012-A 2022-08-00 2022-08-00 PubMed: 35700632 DOI: 10.1016/j.scr.2022.102841Associated cell lines:
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Zhang P, Zheng P, Ji X, Gao Y, Zhang X, Chen Q
Generation of a human induced pluripotent stem cell line (CIPi002-A) from an early infantile epileptic encephalopathy patient with a heterozygous mutation in SCN8A
Zhang P et al. Generation of a human induced pluripotent stem cell line (CIPi002-A) from an early infantile epileptic encephalopathy patient with a heterozygous mutation in SCN8A. . 2022-08-00. Pubmed ID: 35853415; DOI: 10.1016/j.scr.2022.102862 CIPi002-A 2022-08-00 2022-08-00 PubMed: 35853415 DOI: 10.1016/j.scr.2022.102862Associated cell lines:
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Ding Y, Chen H, Zhao J, Wang Y, Deng Y
Generation of two iPSC cell lines (SIAISi020-A and SIAISi019-A) from an 82-year-old mild cognitive impairment (MCI) and her unaffected child from Chinese Han population
Ding Y et al. Generation of two iPSC cell lines (SIAISi020-A and SIAISi019-A) from an 82-year-old mild cognitive impairment (MCI) and her unaffected child from Chinese Han population. . 2022-08-00. Pubmed ID: 35853414; DOI: 10.1016/j.scr.2022.102869 SIAISi019-ASIAISi020-A 2022-08-00 2022-08-00 PubMed: 35853414 DOI: 10.1016/j.scr.2022.102869Associated cell lines:
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Patel A, Iannello G, Diaz AG, Sirabella D, Thaker V, Corneo B
Efficient Cas9-based Genome Editing Using CRISPR Analysis Webtools in Severe Early-onset-obesity Patient-derived iPSCs
Patel A et al. Efficient Cas9-based Genome Editing Using CRISPR Analysis Webtools in Severe Early-onset-obesity Patient-derived iPSCs. . 2022-08-00. Pubmed ID: 35950852; DOI: 10.1002/cpz1.519; PMC: PMC9377717 CUIMCi003-ACUIMCi003-A-1 2022-08-00 2022-08-00 PubMed: 35950852 DOI: 10.1002/cpz1.519Associated cell lines:
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Chen YH, Huang PS, Wen MH, Pan M, Lee DF, Chen TY
Generation of a homozygous knock-in human embryonic stem cell line expressing mEos4b-tagged CTR1
Chen YH et al. Generation of a homozygous knock-in human embryonic stem cell line expressing mEos4b-tagged CTR1. . 2022-08-00. Pubmed ID: 35728441; DOI: 10.1016/j.scr.2022.102845; PMC: PMC9360979 WAe001-AWAe001-A-79 2022-08-00 2022-08-00 PubMed: 35728441 DOI: 10.1016/j.scr.2022.102845Associated cell lines:
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Clayton JS, Suleski I, Vo C, Smith R, Scriba CK, Saker S, Larmonier T, Malfatti E, Romero NB, Houweling PJ, Nowak KJ, Ravenscroft G, Laing NG, Taylor RL
Generation of an induced pluripotent stem cell line from a 3-month-old nemaline myopathy patient with a heterozygous dominant c.515C > A (p.Ala172Glu) variant in the ACTA1 gene
Clayton JS et al. Generation of an induced pluripotent stem cell line from a 3-month-old nemaline myopathy patient with a heterozygous dominant c.515C > A (p.Ala172Glu) variant in the ACTA1 gene. . 2022-08-00. Pubmed ID: 35728439; DOI: 10.1016/j.scr.2022.102829 HPIi003-A 2022-08-00 2022-08-00 PubMed: 35728439 DOI: 10.1016/j.scr.2022.102829Associated cell lines:
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Suleski IS, Smith R, Vo C, Scriba CK, Saker S, Larmonier T, Malfatti E, Romero NB, Houweling PJ, Nowak KJ, Laing NG, Taylor RL, Clayton JS
Generation of two isogenic induced pluripotent stem cell lines from a 1-month-old nemaline myopathy patient harbouring a homozygous recessive c.121C > T (p.Arg39Ter) variant in the ACTA1 gene
Suleski IS et al. Generation of two isogenic induced pluripotent stem cell lines from a 1-month-old nemaline myopathy patient harbouring a homozygous recessive c.121C > T (p.Arg39Ter) variant in the ACTA1 gene. . 2022-08-00. Pubmed ID: 35728440; DOI: 10.1016/j.scr.2022.102830 HPIi004-AHPIi004-B 2022-08-00 2022-08-00 PubMed: 35728440 DOI: 10.1016/j.scr.2022.102830 -
Levine J, Hakim F, Kooy RF, Gozes I
Vineland Adaptive Behavior Scale in a Cohort of Four ADNP Syndrome Patients Implicates Age-Dependent Developmental Delays with Increased Impact of Activities of Daily Living
Levine J et al. Vineland Adaptive Behavior Scale in a Cohort of Four ADNP Syndrome Patients Implicates Age-Dependent Developmental Delays with Increased Impact of Activities of Daily Living. . 2022-08-00. Pubmed ID: 35920977; DOI: 10.1007/s12031-022-02048-0 GENYOi004-A 2022-08-00 2022-08-00 PubMed: 35920977 DOI: 10.1007/s12031-022-02048-0Associated cell lines:
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Ji D, Su X, Hu C, Zhang Z, Wang M, Zou W, Shen L, Liu Y, Liang C, Du Y, Liang D, Cao Y
Generation of an induced pluripotent stem cell line from a patient with leber's hereditary optic neuropathy carrying a homoplasmic m.3635G > A mutation in the mitochondrial ND1 gene
Ji D et al. Generation of an induced pluripotent stem cell line from a patient with leber's hereditary optic neuropathy carrying a homoplasmic m.3635G > A mutation in the mitochondrial ND1 gene. . 2022-08-00. Pubmed ID: 35905669; DOI: 10.1016/j.scr.2022.102858 AHMUi001-A 2022-08-00 2022-08-00 PubMed: 35905669 DOI: 10.1016/j.scr.2022.102858Associated cell lines:
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Lotila J, Hyvärinen T, Skottman H, Airas L, Narkilahti S, Hagman S
Establishment of a human induced pluripotent stem cell line (TAUi008-A) derived from a multiple sclerosis patient
Lotila J et al. Establishment of a human induced pluripotent stem cell line (TAUi008-A) derived from a multiple sclerosis patient. . 2022-08-00. Pubmed ID: 35843021; DOI: 10.1016/j.scr.2022.102865 TAUi008-A 2022-08-00 2022-08-00 PubMed: 35843021 DOI: 10.1016/j.scr.2022.102865Associated cell lines:
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Kim JH, Kang KW, Lee BH, Park Y, Kim BS
Generation of human induced iPSC KUMi003-A from acute promyelocytic leukemia (APL) M3
Kim JH et al. Generation of human induced iPSC KUMi003-A from acute promyelocytic leukemia (APL) M3. . 2022-08-00. Pubmed ID: 35905670; DOI: 10.1016/j.scr.2022.102861 KUMi001-AKUMi002-AKUMi003-A 2022-08-00 2022-08-00 PubMed: 35905670 DOI: 10.1016/j.scr.2022.102861 -
D'Anzi A, Perciballi E, Ruotolo G, Ferrari D, Notaro A, Lombardi I, Gelati M, Frezza K, Bernardini L, Torrente I, De Luca A, La Bella V, Luigi Vescovi A, Rosati J
Production of CSSi013-A (9360) iPSC line from an asymptomatic subject carrying an heterozygous mutation in TDP-43 protein
D'Anzi A et al. Production of CSSi013-A (9360) iPSC line from an asymptomatic subject carrying an heterozygous mutation in TDP-43 protein. . 2022-08-00. Pubmed ID: 35714448; DOI: 10.1016/j.scr.2022.102835 CSSi011-ACSSi013-A 2022-08-00 2022-08-00 PubMed: 35714448 DOI: 10.1016/j.scr.2022.102835 -
Ding C, Tan F, Zhou Y, Duan C, Gu J, Cui Z, Chen Z, Tang S, Chen J
Establishment of a human induced pluripotent stem cell line (CSUASOi010-A) by reprogramming peripheral blood mononuclear cells of a type 2 diabetic mellitus patient
Ding C et al. Establishment of a human induced pluripotent stem cell line (CSUASOi010-A) by reprogramming peripheral blood mononuclear cells of a type 2 diabetic mellitus patient. . 2022-08-00. Pubmed ID: 35841806; DOI: 10.1016/j.scr.2022.102851 CSUASOi010-A 2022-08-00 2022-08-00 PubMed: 35841806 DOI: 10.1016/j.scr.2022.102851Associated cell lines:
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Cao S, Guo R, Zhang J, Liu X, Zhou Z, Song Y, Ma J
Human induced pluripotent stem cells generated from a 45-years-old male donor of type 2 diabetes mellitus with APOE-epsilon3/epsilon3 alleles
Cao S et al. Human induced pluripotent stem cells generated from a 45-years-old male donor of type 2 diabetes mellitus with APOE-epsilon3/epsilon3 alleles. . 2022-08-00. Pubmed ID: 35717858; DOI: 10.1016/j.scr.2022.102840 HEBHMUi001-AHEBHMUi012-A 2022-08-00 2022-08-00 PubMed: 35717858 DOI: 10.1016/j.scr.2022.102840Associated cell lines:
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Bhargava N, Thakur P, Muruganandam TP, Jaitly S, Gupta P, Lohani N, Goswami SG, Saravanakumar V, Bhattacharya SK, Jain S, Ramalingam S
Development of an efficient single-cell cloning and expansion strategy for genome edited induced pluripotent stem cells
Bhargava N et al. Development of an efficient single-cell cloning and expansion strategy for genome edited induced pluripotent stem cells. . 2022-08-00. Pubmed ID: 35637316; DOI: 10.1007/s11033-022-07621-9 IGIBi001-AIGIBi002-A 2022-08-00 2022-08-00 PubMed: 35637316 DOI: 10.1007/s11033-022-07621-9Associated cell lines:
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Suwanpitak S, Chanprasert C, Netsrithong R, Plengvidhya N, Yenchitsommanus PT, Wattanapanitch M, Thamtarana PJ
Generation of an induced pluripotent stem cell line (MUSIi015-A) from a diabetic patient carrying mutations in ZYG11A (p.L475P) and GATA6 (p.E51K)
Suwanpitak S et al. Generation of an induced pluripotent stem cell line (MUSIi015-A) from a diabetic patient carrying mutations in ZYG11A (p.L475P) and GATA6 (p.E51K). . 2022-08-00. Pubmed ID: 35853413; DOI: 10.1016/j.scr.2022.102871 MUSIi015-A 2022-08-00 2022-08-00 PubMed: 35853413 DOI: 10.1016/j.scr.2022.102871Associated cell lines:
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Kim H, Kim HJ, Oh J, Lee ST, Won D, Choi HK, Choi JR, Kim S, Kim HP, Kim SJ, Park SW, Kang SM, Lee SH
An induced pluripotent stem cell line (YCMi006-A) generated from a patient with hypertrophic cardiomyopathy who carries the ACTA1 mutation p.Ile343Met
Kim H et al. An induced pluripotent stem cell line (YCMi006-A) generated from a patient with hypertrophic cardiomyopathy who carries the ACTA1 mutation p.Ile343Met. . 2022-08-00. Pubmed ID: 35917599; DOI: 10.1016/j.scr.2022.102874 YCMi006-A 2022-08-00 2022-08-00 PubMed: 35917599 DOI: 10.1016/j.scr.2022.102874Associated cell lines:
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Martínez-Moreno R, Carreras D, Aran B, Kuebler B, Sarquella-Brugada G, Brugada R, Pérez GJ, Scornik FS, Selga E
Generation of four induced pluripotent stem cell lines from a family harboring a single nucleotide variant in SCN5A
Martínez-Moreno R et al. Generation of four induced pluripotent stem cell lines from a family harboring a single nucleotide variant in SCN5A. . 2022-08-00. Pubmed ID: 35772296; DOI: 10.1016/j.scr.2022.102847 IDIBGIi002-AIDIBGIi003-AIDIBGIi004-AIDIBGIi005-A 2022-08-00 2022-08-00 PubMed: 35772296 DOI: 10.1016/j.scr.2022.102847Associated cell lines:
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Altmaier S, Meiser I, Lemesre E, Chanrion B, Steeg R, Leonte LE, Holst B, Nielsen BS, Clausen C, Schmidt K, Vinggaard AM, Zimmermann H, Neubauer JC, Rasmussen MA
Human iPSC-derived hepatocytes in 2D and 3D suspension culture for cryopreservation and in vitro toxicity studies
Altmaier S et al. Human iPSC-derived hepatocytes in 2D and 3D suspension culture for cryopreservation and in vitro toxicity studies. . 2022-08-00. Pubmed ID: 35598806; DOI: 10.1016/j.reprotox.2022.05.005 BIONi010-C-64 2022-08-00 2022-08-00 PubMed: 35598806 DOI: 10.1016/j.reprotox.2022.05.005Associated cell lines:
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Zhong R, Schimanski T, Zhang F, Lan H, Hohn A, Xu Q, Huang M, Liao Z, Qiao L, Yang Z, Li Y, Zhao Z, Li X, Rose L, Albers S, Maywald L, Müller J, Dinkel H, Saguner A, Janssen JWG, Swamy N, Xi Y, Lang S, Kleinsorge M, Duru F, Zhou X, Diecke S, Cyganek L, Akin I, El-Battrawy I
A Preclinical Study on Brugada Syndrome with a CACNB2 Variant Using Human Cardiomyocytes from Induced Pluripotent Stem Cells
Zhong R et al. A Preclinical Study on Brugada Syndrome with a CACNB2 Variant Using Human Cardiomyocytes from Induced Pluripotent Stem Cells. . 2022-07-27. Pubmed ID: 35955449; DOI: 10.3390/ijms23158313; PMC: PMC9368582 UMGi124-AUMGi014-BBIHi259-ABIHi259-A-1 2022-07-27 2022-07-27 PubMed: 35955449 DOI: 10.3390/ijms23158313Associated cell lines:
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Solomon S, Sampathkumar NK, Carre I, Mondal M, Chennell G, Vernon AC, Ruepp MD, Mitchell JC
Heterozygous expression of the Alzheimer's disease-protective PLCγ2 P522R variant enhances Aβ clearance while preserving synapses
Solomon S et al. Heterozygous expression of the Alzheimer's disease-protective PLCγ2 P522R variant enhances Aβ clearance while preserving synapses. . 2022-07-27. Pubmed ID: 35895133; DOI: 10.1007/s00018-022-04473-1; PMC: PMC9329165 BIONi010-C 2022-07-27 2022-07-27 PubMed: 35895133 DOI: 10.1007/s00018-022-04473-1Associated cell lines:
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Langston RG, Beilina A, Reed X, Kaganovich A, Singleton AB, Blauwendraat C, Gibbs JR, Cookson MR
Association of a common genetic variant with Parkinson's disease is mediated by microglia
Langston RG et al. Association of a common genetic variant with Parkinson's disease is mediated by microglia. . 2022-07-27. Pubmed ID: 35895835; DOI: 10.1126/scitranslmed.abp8869; PMC: PMC9809150 CDIi015-ACDIi016-ACDIi017-ACDIi018-ACDIi023-ACDIi027-ACDIi028-ACDIi047-ACDIi048-ACDIi063-ACDIi072-ACDIi078-ACDIi093-A 2022-07-27 2022-07-27 PubMed: 35895835 DOI: 10.1126/scitranslmed.abp8869 -
Salmina AB, Malinovskaya NA, Morgun AV, Khilazheva ED, Uspenskaya YA, Illarioshkin SN
Reproducibility of developmental neuroplasticity in in vitro brain tissue models
Salmina AB et al. Reproducibility of developmental neuroplasticity in in vitro brain tissue models. . 2022-07-26. Pubmed ID: 34983132; DOI: 10.1515/revneuro-2021-0137 RCPCMi004-AICGi018-ARCPCMi008-A 2022-07-26 2022-07-26 PubMed: 34983132 DOI: 10.1515/revneuro-2021-0137Associated cell lines:
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Ma Y, Sun W, Zhao L, Yao M, Wu C, Su P, Yang L, Wang G
Generation of an mESC model with a human hemophilia B nonsense mutation via CRISPR/Cas9 technology
Ma Y et al. Generation of an mESC model with a human hemophilia B nonsense mutation via CRISPR/Cas9 technology. . 2022-07-26. Pubmed ID: 35883203; DOI: 10.1186/s13287-022-03036-2; PMC: PMC9327398 SXMUi001-A 2022-07-26 2022-07-26 PubMed: 35883203 DOI: 10.1186/s13287-022-03036-2Associated cell lines:
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Dan Z.
Research progress of androgen insensitivity syndrome
Dan Z.. Research progress of androgen insensitivity syndrome. . 2022-07-25. DOI: 10.3760/cma.j.cn101441-20210226-00088 SKLRMi001-A 2022-07-25 2022-07-25 DOI: 10.3760/cma.j.cn101441-20210226-00088Associated cell lines:
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Tasca F, Brescia M, Wang Q, Liu J, Janssen JM, Szuhai K, Gonçalves MAFV
Large-scale genome editing based on high-capacity adenovectors and CRISPR-Cas9 nucleases rescues full-length dystrophin synthesis in DMD muscle cells
Tasca F et al. Large-scale genome editing based on high-capacity adenovectors and CRISPR-Cas9 nucleases rescues full-length dystrophin synthesis in DMD muscle cells. . 2022-07-22. Pubmed ID: 35776127; DOI: 10.1093/nar/gkac567; PMC: PMC9303392 CENSOi001-B 2022-07-22 2022-07-22 PubMed: 35776127 DOI: 10.1093/nar/gkac567Associated cell lines:
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Zhai F, Li J, Ye M, Jin X
The functions and effects of CUL3-E3 ligases mediated non-degradative ubiquitination
Zhai F et al. The functions and effects of CUL3-E3 ligases mediated non-degradative ubiquitination. . 2022-07-20. Pubmed ID: 35580799; DOI: 10.1016/j.gene.2022.146562 PSHi002-A 2022-07-20 2022-07-20 PubMed: 35580799 DOI: 10.1016/j.gene.2022.146562Associated cell lines:
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Holzer AK, Karreman C, Suciu I, Furmanowsky LS, Wohlfarth H, Loser D, Dirks WG, Pardo González E, Leist M
Generation of Human Nociceptor-Enriched Sensory Neurons for the Study of Pain-Related Dysfunctions
Holzer AK et al. Generation of Human Nociceptor-Enriched Sensory Neurons for the Study of Pain-Related Dysfunctions. . 2022-07-20. Pubmed ID: 35689659; DOI: 10.1093/stcltm/szac031; PMC: PMC9299516 SIGi001-A 2022-07-20 2022-07-20 PubMed: 35689659 DOI: 10.1093/stcltm/szac031Associated cell lines:
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Danese A, Patergnani S, Maresca A, Peron C, Raimondi A, Caporali L, Marchi S, La Morgia C, Del Dotto V, Zanna C, Iannielli A, Segnali A, Di Meo I, Cavaliere A, Lebiedzinska-Arciszewska M, Wieckowski MR, Martinuzzi A, Moraes-Filho MN, Salomao SR, Berezovsky A, Belfort R Jr, Buser C, Ross-Cisneros FN, Sadun AA, Tacchetti C, Broccoli V, Giorgi C, Tiranti V, Carelli V, Pinton P
Pathological mitophagy disrupts mitochondrial homeostasis in Leber's hereditary optic neuropathy
Danese A et al. Pathological mitophagy disrupts mitochondrial homeostasis in Leber's hereditary optic neuropathy. . 2022-07-19. Pubmed ID: 35858578; DOI: 10.1016/j.celrep.2022.111124; PMC: PMC9314546 FINCBi001-A 2022-07-19 2022-07-19 PubMed: 35858578 DOI: 10.1016/j.celrep.2022.111124Associated cell lines:
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Astro V, Ramirez-Calderon G, Pennucci R, Caroli J, Saera-Vila A, Cardona-Londoño K, Forastieri C, Fiacco E, Maksoud F, Alowaysi M, Sogne E, Falqui A, Gonzàlez F, Montserrat N, Battaglioli E, Mattevi A, Adamo A
Fine-tuned KDM1A alternative splicing regulates human cardiomyogenesis through an enzymatic-independent mechanism
Astro V et al. Fine-tuned KDM1A alternative splicing regulates human cardiomyogenesis through an enzymatic-independent mechanism. . 2022-07-15. Pubmed ID: 35856020; DOI: 10.1016/j.isci.2022.104665; PMC: PMC9287196 WAe001-A 2022-07-15 2022-07-15 PubMed: 35856020 DOI: 10.1016/j.isci.2022.104665Associated cell lines:
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Yamane J, Wada T, Otsuki H, Inomata K, Suzuki M, Hisaki T, Sekine S, Kouzuki H, Kobayashi K, Sone H, Yamashita JK, Osawa M, Saito MK, Fujibuchi W
StemPanTox: A fast and wide-target drug assessment system for tailor-made safety evaluations using personalized iPS cells
Yamane J et al. StemPanTox: A fast and wide-target drug assessment system for tailor-made safety evaluations using personalized iPS cells. . 2022-07-15. Pubmed ID: 35754715; DOI: 10.1016/j.isci.2022.104538; PMC: PMC9218511 KUIMSe003-A 2022-07-15 2022-07-15 PubMed: 35754715 DOI: 10.1016/j.isci.2022.104538Associated cell lines:
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Bartalska K, Hübschmann V, Korkut-Demirbaş M, Cubero RJA, Venturino A, Rössler K, Czech T, Siegert S
A systematic characterization of microglia-like cell occurrence during retinal organoid differentiation
Bartalska K et al. A systematic characterization of microglia-like cell occurrence during retinal organoid differentiation. . 2022-07-15. Pubmed ID: 35789843; DOI: 10.1016/j.isci.2022.104580; PMC: PMC9250027 CRMi001-A 2022-07-15 2022-07-15 PubMed: 35789843 DOI: 10.1016/j.isci.2022.104580Associated cell lines:
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Ávila-González D, Portillo W, Barragán-Álvarez CP, Hernandez-Montes G, Flores-Garza E, Molina-Hernández A, Díaz-Martínez NE, Díaz NF
The human amniotic epithelium confers a bias to differentiate toward the neuroectoderm lineage in human embryonic stem cells
Ávila-González D et al. The human amniotic epithelium confers a bias to differentiate toward the neuroectoderm lineage in human embryonic stem cells. . 2022-07-11. Pubmed ID: 35815953; DOI: 10.7554/elife.68035; PMC: PMC9313526 INPERe001-A 2022-07-11 2022-07-11 PubMed: 35815953 DOI: 10.7554/elife.68035Associated cell lines:
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Abeditashi M, Weber JJ, Pereira Sena P, Velic A, Kalimeri M, Incebacak Eltemur RD, Schmidt J, Hübener-Schmid J, Hauser S, Macek B, Riess O, Schmidt T
KPNB1 modulates the Machado-Joseph disease protein ataxin-3 through activation of the mitochondrial protease CLPP
Abeditashi M et al. KPNB1 modulates the Machado-Joseph disease protein ataxin-3 through activation of the mitochondrial protease CLPP. . 2022-07-06. Pubmed ID: 35794401; DOI: 10.1007/s00018-022-04372-5; PMC: PMC9259533 HIHCNi002-A 2022-07-06 2022-07-06 PubMed: 35794401 DOI: 10.1007/s00018-022-04372-5Associated cell lines:
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Navinés-Ferrer A, Ruiz-Nogales S, Navarro R, Pomares E
Impaired Bestrophin Channel Activity in an iPSC-RPE Model of Best Vitelliform Macular Dystrophy (BVMD) from an Early Onset Patient Carrying the P77S Dominant Mutation
Navinés-Ferrer A et al. Impaired Bestrophin Channel Activity in an iPSC-RPE Model of Best Vitelliform Macular Dystrophy (BVMD) from an Early Onset Patient Carrying the P77S Dominant Mutation. . 2022-07-04. Pubmed ID: 35806438; DOI: 10.3390/ijms23137432; PMC: PMC9266689 FRIMOi005-AFRIMOi006-A 2022-07-04 2022-07-04 PubMed: 35806438 DOI: 10.3390/ijms23137432Associated cell lines:
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Liu Y, Li X, Zhao X, Dong J, Zhang C, Lin T
Establishment of a human iPSC (ZZUNEUi026-A) from a dilated cardiomyopathy patient carrying heterozygous Vinculin (c. 625A > T) mutant
Liu Y et al. Establishment of a human iPSC (ZZUNEUi026-A) from a dilated cardiomyopathy patient carrying heterozygous Vinculin (c. 625A > T) mutant. . 2022-07-00. Pubmed ID: 35567849; DOI: 10.1016/j.scr.2022.102812 ZZUNEUi026-A 2022-07-00 2022-07-00 PubMed: 35567849 DOI: 10.1016/j.scr.2022.102812Associated cell lines:
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Guo F, Sun Y, Wang H, Wang H, Zhou J, Fan H, Su J, Gong T, Jiang C, Liang P
Generation of an induced pluripotent stem cell line from a long QT syndrome patient carrying KCNH2/1956C > A mutation
Guo F et al. Generation of an induced pluripotent stem cell line from a long QT syndrome patient carrying KCNH2/1956C > A mutation. . 2022-07-00. Pubmed ID: 35569348; DOI: 10.1016/j.scr.2022.102813 ZJUi010-A 2022-07-00 2022-07-00 PubMed: 35569348 DOI: 10.1016/j.scr.2022.102813Associated cell lines:
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Sanjaya R, Sari SY, Faisal AI, Prawira MA, Faza N, Widyastuti HP, Murti H
The first reported generation of footprint-free human induced pluripotent stem cell line (SCIKFi001-A) in Indonesia from cGMP grade umbilical cord-derived mesenchymal stem cells (UC-MSCs) using synthetic self-replicating RNA
Sanjaya R et al. The first reported generation of footprint-free human induced pluripotent stem cell line (SCIKFi001-A) in Indonesia from cGMP grade umbilical cord-derived mesenchymal stem cells (UC-MSCs) using synthetic self-replicating RNA. . 2022-07-00. Pubmed ID: 35462157; DOI: 10.1016/j.scr.2022.102790 SCIKFi001-A 2022-07-00 2022-07-00 PubMed: 35462157 DOI: 10.1016/j.scr.2022.102790Associated cell lines:
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Dong T, Zhao Y, Jin HF, Shen L, Lin Y, Si LL, Chen L, Liu JC
SNTA1-deficient human cardiomyocytes demonstrate hypertrophic phenotype and calcium handling disorder
Dong T et al. SNTA1-deficient human cardiomyocytes demonstrate hypertrophic phenotype and calcium handling disorder. . 2022-06-30. Pubmed ID: 35773684; DOI: 10.1186/s13287-022-02955-4; PMC: PMC9248201 WAe009-AWAe009-A-50 2022-06-30 2022-06-30 PubMed: 35773684 DOI: 10.1186/s13287-022-02955-4Associated cell lines:
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Han Z, Wang J, Luan J, Cui Y, Han J
Establishment of a control induced pluripotent stem cell line SMBCi018-A from a patient with congenital talipes equinovarus
Han Z et al. Establishment of a control induced pluripotent stem cell line SMBCi018-A from a patient with congenital talipes equinovarus. . 2022-07-00. Pubmed ID: 35605480; DOI: 10.1016/j.scr.2022.102814 SMBCi009-ASMBCi018-A 2022-07-00 2022-07-00 PubMed: 35605480 DOI: 10.1016/j.scr.2022.102814Associated cell lines:
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Liu W, Liu T, Xiao T, Xie L, Hou C, Jiang X
Generation of an induced pluripotent stem cell line from a Chinese Han child with catecholaminergic polymorphic ventricular tachycardia
Liu W et al. Generation of an induced pluripotent stem cell line from a Chinese Han child with catecholaminergic polymorphic ventricular tachycardia. . 2022-07-00. Pubmed ID: 35679758; DOI: 10.1016/j.scr.2022.102811 SHETi003-A 2022-07-00 2022-07-00 PubMed: 35679758 DOI: 10.1016/j.scr.2022.102811Associated cell lines:
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Yu Q, Mehta A, Zou J, Beers J, de Jesus Rasheed AA, Goldbach-Mansky R, Boehm M, Chen G
Human induced pluripotent stem cells generated from Chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature (CANDLE) syndrome patients with a homozygous mutation in the PSMB8 gene (NIHTVBi016-A, NIHTVBi017-A, NIHTVBi018-A)
Yu Q et al. Human induced pluripotent stem cells generated from Chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature (CANDLE) syndrome patients with a homozygous mutation in the PSMB8 gene (NIHTVBi016-A, NIHTVBi017-A, NIHTVBi018-A). . 2022-07-00. Pubmed ID: 35660921; DOI: 10.1016/j.scr.2022.102820; PMC: PMC9514390 NIHTVBi016-ANIHTVBi017-ANIHTVBi018-A 2022-07-00 2022-07-00 PubMed: 35660921 DOI: 10.1016/j.scr.2022.102820Associated cell lines:
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Luan J, Zou H, Cui Y, Wang J, Han Z, Zhang G, Han J
Generation of induced pluripotent stem cells named SMBCi019-A from a methylmalonic acidemia patient carrying the MMACHC mutations
Luan J et al. Generation of induced pluripotent stem cells named SMBCi019-A from a methylmalonic acidemia patient carrying the MMACHC mutations. . 2022-07-00. Pubmed ID: 35660814; DOI: 10.1016/j.scr.2022.102821 SMBCi019-A 2022-07-00 2022-07-00 PubMed: 35660814 DOI: 10.1016/j.scr.2022.102821Associated cell lines:
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Li S, Zhu Q, Cai Y, Yang Q
Generation of an induced pluripotent stem cell line from a patient with Angelman syndrome carrying UBE3A mutation
Li S et al. Generation of an induced pluripotent stem cell line from a patient with Angelman syndrome carrying UBE3A mutation. . 2022-07-00. Pubmed ID: 35489268; DOI: 10.1016/j.scr.2022.102791 WMUi032-A 2022-07-00 2022-07-00 PubMed: 35489268 DOI: 10.1016/j.scr.2022.102791Associated cell lines:
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Beghin A, Grenci G, Sahni G, Guo S, Rajendiran H, Delaire T, Mohamad Raffi SB, Blanc D, de Mets R, Ong HT, Galindo X, Monet A, Acharya V, Racine V, Levet F, Galland R, Sibarita JB, Viasnoff V
Automated high-speed 3D imaging of organoid cultures with multi-scale phenotypic quantification
Beghin A et al. Automated high-speed 3D imaging of organoid cultures with multi-scale phenotypic quantification. . 2022-07-00. Pubmed ID: 35697835; DOI: 10.1038/s41592-022-01508-0 IMAGINi004-AIMAGINi005-A 2022-07-00 2022-07-00 PubMed: 35697835 DOI: 10.1038/s41592-022-01508-0Associated cell lines:
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Zhang Y, Zhu J, Dai Y, Wang L, Liu R, Guo X
Generation of an induced pluripotent stem cell line (ZZUi034-A) from a 65 year old Chinese female donor with sendai virus reprogramming protocol
Zhang Y et al. Generation of an induced pluripotent stem cell line (ZZUi034-A) from a 65 year old Chinese female donor with sendai virus reprogramming protocol. . 2022-07-00. Pubmed ID: 35462158; DOI: 10.1016/j.scr.2022.102788 ZZUi034-A 2022-07-00 2022-07-00 PubMed: 35462158 DOI: 10.1016/j.scr.2022.102788Associated cell lines:
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DeRosa BA, Simon SA, Velez CA, Vance JM, Pericak-Vance MA, Dykxhoorn DM
Generation of two iPSC lines (UMi038-A & UMi039-A) from siblings bearing an Alzheimer's disease-associated variant in SORL1
DeRosa BA et al. Generation of two iPSC lines (UMi038-A & UMi039-A) from siblings bearing an Alzheimer's disease-associated variant in SORL1. . 2022-07-00. Pubmed ID: 35671596; DOI: 10.1016/j.scr.2022.102823 UMi038-AUMi039-AUMi039-A-1 2022-07-00 2022-07-00 PubMed: 35671596 DOI: 10.1016/j.scr.2022.102823Associated cell lines:
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Shi Y, Wu S, Yang B, Yu B, Yan Y, Yang J, Chu M, Hu X
Generation of a human iPSC line CIBi011-A from amniocytes of a healthy fetus
Shi Y et al. Generation of a human iPSC line CIBi011-A from amniocytes of a healthy fetus. . 2022-07-00. Pubmed ID: 35609349; DOI: 10.1016/j.scr.2022.102801 CIBi008-ACIBi011-A 2022-07-00 2022-07-00 PubMed: 35609349 DOI: 10.1016/j.scr.2022.102801 -
Fu J, Jiang L, Yu B, Liu Y, Wei R, Hu Y, Ho WI, Yang B, Chu M, Tse HF, Yang J
Generation of a human iPSC line CIBi010-A with a reporter for ASGR1 using CRISPR/Cas9
Fu J et al. Generation of a human iPSC line CIBi010-A with a reporter for ASGR1 using CRISPR/Cas9. . 2022-07-00. Pubmed ID: 35561459; DOI: 10.1016/j.scr.2022.102800 CIBi010-A 2022-07-00 2022-07-00 PubMed: 35561459 DOI: 10.1016/j.scr.2022.102800Associated cell lines:
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Doeser MC, Krygin J, Röpke A, Han D, Wedlich-Söldner R, Schöler HR, Pavenstädt H, Kim KP
Generation of a human iPSC line (MPIi008-A) from a patient with Denys-Drash syndrome
Doeser MC et al. Generation of a human iPSC line (MPIi008-A) from a patient with Denys-Drash syndrome. . 2022-07-00. Pubmed ID: 35667217; DOI: 10.1016/j.scr.2022.102826 MPIi008-A 2022-07-00 2022-07-00 PubMed: 35667217 DOI: 10.1016/j.scr.2022.102826Associated cell lines:
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Zaw K, Carvalho LS, Aung-Htut MT, Fletcher S, Wilton SD, Chen FK, McLenachan S
Pathogenesis and Treatment of Usher Syndrome Type IIA
Zaw K et al. Pathogenesis and Treatment of Usher Syndrome Type IIA. . 2022-07-00. Pubmed ID: 36041150; DOI: 10.1097/apo.0000000000000546 IISHDOi004-AINMi001-AINMi002-AFRIMOi002-AINMi005-AKLRMMEi002-A 2022-07-00 2022-07-00 PubMed: 36041150 DOI: 10.1097/apo.0000000000000546Associated cell lines:
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Waqas SF, Sohail A, Nguyen AHH, Usman A, Ludwig T, Wegner A, Malik MNH, Schuchardt S, Geffers R, Winterhoff M, Merkert S, Martin U, Olmer R, Lachmann N, Pessler F
ISG15 deficiency features a complex cellular phenotype that responds to treatment with itaconate and derivatives
Waqas SF et al. ISG15 deficiency features a complex cellular phenotype that responds to treatment with itaconate and derivatives. . 2022-07-00. Pubmed ID: 35842904; DOI: 10.1002/ctm2.931; PMC: PMC9288839 MHHi001-AMHHi001-A-3 2022-07-00 2022-07-00 PubMed: 35842904 DOI: 10.1002/ctm2.931Associated cell lines:
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Humphreys PA, Mancini FE, Ferreira MJS, Woods S, Ogene L, Kimber SJ
Developmental principles informing human pluripotent stem cell differentiation to cartilage and bone
Humphreys PA et al. Developmental principles informing human pluripotent stem cell differentiation to cartilage and bone. . 2022-07-00. Pubmed ID: 34949507; DOI: 10.1016/j.semcdb.2021.11.024 MCRIi001-AMCRIi001-A-1MCRIi001-A-2MCRIi019-AMCRIi001-BMCRIi019-A-2MCRIi001-A-3MCRIi001-A-4 2022-07-00 2022-07-00 PubMed: 34949507 DOI: 10.1016/j.semcdb.2021.11.024Associated cell lines:
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He Z, Feng K, Sun H, Yu T, Zhu D, Yang Y
Generation of a human extended pluripotent stem cell line (SKLRMe002-A) carrying a doxycycline-inducible Cas9 expression cassette
He Z et al. Generation of a human extended pluripotent stem cell line (SKLRMe002-A) carrying a doxycycline-inducible Cas9 expression cassette. . 2022-07-00. Pubmed ID: 35617843; DOI: 10.1016/j.scr.2022.102816 SKLRMe002-A 2022-07-00 2022-07-00 PubMed: 35617843 DOI: 10.1016/j.scr.2022.102816Associated cell lines:
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Luan J, Cui Y, Wang J, Liang Y, Zhao Y, Zhang G, Han J
Generation of a non-integrated induced pluripotent stem cell line from urine cells of a Chinese osteogenesis imperfecta type I patient
Luan J et al. Generation of a non-integrated induced pluripotent stem cell line from urine cells of a Chinese osteogenesis imperfecta type I patient. . 2022-07-00. Pubmed ID: 35660813; DOI: 10.1016/j.scr.2022.102827 SMBCi014-A 2022-07-00 2022-07-00 PubMed: 35660813 DOI: 10.1016/j.scr.2022.102827Associated cell lines:
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Fortune AJ, Taylor BV, Charlesworth JC, Burdon KP, Blackburn NB, Fletcher JL, Mehta A, Young KM
Generation and characterisation of four multiple sclerosis iPSC lines from a single family
Fortune AJ et al. Generation and characterisation of four multiple sclerosis iPSC lines from a single family. . 2022-07-00. Pubmed ID: 35679759; DOI: 10.1016/j.scr.2022.102828 MNZTASi001-AMNZTASi002-AMNZTASi003-AMNZTASi004-AMNZTASi005-A 2022-07-00 2022-07-00 PubMed: 35679759 DOI: 10.1016/j.scr.2022.102828Associated cell lines:
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Martello F, Lattante S, Doronzio PN, Conte A, Bisogni G, Orteschi D, Luigetti M, Marrucci MA, Zollino M, Sabatelli M, Marangi G
Generation of an induced pluripotent stem cell line (UCSCi002-A) from a patient with a variant in TARDBP gene associated with familial amyotrophic lateral sclerosis and frontotemporal dementia
Martello F et al. Generation of an induced pluripotent stem cell line (UCSCi002-A) from a patient with a variant in TARDBP gene associated with familial amyotrophic lateral sclerosis and frontotemporal dementia. . 2022-07-00. Pubmed ID: 35667216; DOI: 10.1016/j.scr.2022.102825 UCSCi002-A 2022-07-00 2022-07-00 PubMed: 35667216 DOI: 10.1016/j.scr.2022.102825Associated cell lines:
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Mencke P, Boussaad I, Önal G, Kievit AJA, Boon AJW, Mandemakers W, Bonifati V, Krüger R
Generation and characterization of a genetic Parkinson's disease-patient derived iPSC line DJ-1-delP (LCSBi008-A)
Mencke P et al. Generation and characterization of a genetic Parkinson's disease-patient derived iPSC line DJ-1-delP (LCSBi008-A). . 2022-07-00. Pubmed ID: 35500378; DOI: 10.1016/j.scr.2022.102792 LCSBi008-A 2022-07-00 2022-07-00 PubMed: 35500378 DOI: 10.1016/j.scr.2022.102792Associated cell lines:
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Nhung Nguyen TH, Trinh Tran TT, Luong TH, Nguyen XH
Generation of an erythroid progenitor-derived iPSC line, VRISGi002-A, from a healthy 27-year-old Vietnamese donor under a feeder-free system
Nhung Nguyen TH et al. Generation of an erythroid progenitor-derived iPSC line, VRISGi002-A, from a healthy 27-year-old Vietnamese donor under a feeder-free system. . 2022-07-00. Pubmed ID: 35679757; DOI: 10.1016/j.scr.2022.102824 VRISGi001-AVRISGi002-A 2022-07-00 2022-07-00 PubMed: 35679757 DOI: 10.1016/j.scr.2022.102824Associated cell lines:
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Mencke P, Hanss Z, Jarazo J, Massart F, Rybicki A, Petkovski E, Glaab E, Boussaad I, Bonifati V, Christian Schwamborn J, Mandemakers W, Krüger R
Generation of isogenic control DJ-1-delP GC13 for the genetic Parkinson's disease-patient derived iPSC line DJ-1-delP (LCSBi008-A-1)
Mencke P et al. Generation of isogenic control DJ-1-delP GC13 for the genetic Parkinson's disease-patient derived iPSC line DJ-1-delP (LCSBi008-A-1). . 2022-07-00. Pubmed ID: 35617842; DOI: 10.1016/j.scr.2022.102815 LCSBi001-ALCSBi008-ALCSBi008-A-1 2022-07-00 2022-07-00 PubMed: 35617842 DOI: 10.1016/j.scr.2022.102815Associated cell lines:
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Li X, Gao X, Huang S, Han M, Kang D, Yang J, Wu X, Zheng Q, Yuan Y, Dai P, Wang G
Establishment of an iPSC line (CPGHi005-A) from a patient with Waardenburg syndrome carrying a heterozygous SVA-F retrotransposon insertion into SOX10
Li X et al. Establishment of an iPSC line (CPGHi005-A) from a patient with Waardenburg syndrome carrying a heterozygous SVA-F retrotransposon insertion into SOX10. . 2022-07-00. Pubmed ID: 35691110; DOI: 10.1016/j.scr.2022.102831 CPGHi005-A 2022-07-00 2022-07-00 PubMed: 35691110 DOI: 10.1016/j.scr.2022.102831Associated cell lines:
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Wang X, Shi Z, Lu HY, Kim JJ, Bu W, Villalobos JA, Perera DN, Jung SY, Wang T, Grimm SL, Taylor BC, Rajapakshe K, Park H, Wulfkuhle J, Young NL, Li Y, Coarfa C, Edwards DP, Huang S
High-throughput profiling of histone post-translational modifications and chromatin modifying proteins by reverse phase protein array
Wang X et al. High-throughput profiling of histone post-translational modifications and chromatin modifying proteins by reverse phase protein array. . 2022-06-30. Pubmed ID: 35489683; DOI: 10.1016/j.jprot.2022.104596; PMC: PMC10165948 BCMi001-A 2022-06-30 2022-06-30 PubMed: 35489683 DOI: 10.1016/j.jprot.2022.104596Associated cell lines:
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Chakrabarty K, Prashanthi KN, Shetty R, Argulwar S, Jeyabalan N, Ghosh A
Generation of iPSC line (GLNNFi001-A) from peripheral blood mononuclear cells of a patient with macular corneal dystrophy
Chakrabarty K et al. Generation of iPSC line (GLNNFi001-A) from peripheral blood mononuclear cells of a patient with macular corneal dystrophy. . 2022-07-00. Pubmed ID: 35472829; DOI: 10.1016/j.scr.2022.102789 GLNNFi001-A 2022-07-00 2022-07-00 PubMed: 35472829 DOI: 10.1016/j.scr.2022.102789Associated cell lines:
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Wen H, Sun L, Zhong J, Wu F
Establishment of human embryonic stem cell WAe009-A-88 carrying a long QT syndrome mutation in KCNH2
Wen H et al. Establishment of human embryonic stem cell WAe009-A-88 carrying a long QT syndrome mutation in KCNH2. . 2022-07-00. Pubmed ID: 35526388; DOI: 10.1016/j.scr.2022.102795 WAe009-AWAe009-A-88 2022-07-00 2022-07-00 PubMed: 35526388 DOI: 10.1016/j.scr.2022.102795Associated cell lines:
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Schröter J, Syring H, Göhring G, Kölker S, Opladen T, Hoffmann GF, Syrbe S, Jung-Klawitter S
Generation of an induced pluripotent stem cell line (DHMCi008-A) from an individual with TUBA1A tubulinopathy
Schröter J et al. Generation of an induced pluripotent stem cell line (DHMCi008-A) from an individual with TUBA1A tubulinopathy. . 2022-07-00. Pubmed ID: 35636247; DOI: 10.1016/j.scr.2022.102818 DHMCi008-A 2022-07-00 2022-07-00 PubMed: 35636247 DOI: 10.1016/j.scr.2022.102818Associated cell lines:
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de Jong S, Koolen L, Vázquez-Domínguez I, de Breuk A, Albert S, Hoyng CB, Katti S, den Hollander AI, Garanto A
Generation of an iPSC line (SCTCi014-A) and isogenic control line (SCTCi014-A-1) from an age-related macular degeneration patient carrying the variant c.355G>A in the CFI gene
de Jong S et al. Generation of an iPSC line (SCTCi014-A) and isogenic control line (SCTCi014-A-1) from an age-related macular degeneration patient carrying the variant c.355G>A in the CFI gene. . 2022-07-00. Pubmed ID: 35526386; DOI: 10.1016/j.scr.2022.102797 SCTCi014-ASCTCi014-A-1SCTCi016-A 2022-07-00 2022-07-00 PubMed: 35526386 DOI: 10.1016/j.scr.2022.102797Associated cell lines:
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Hattori A, Ohta E, Nagai M, Iwabuchi K, Okano H
A new approach to analysis of intracellular proteins and subcellular localization using cellprofiler and imageJ in combination
Hattori A et al. A new approach to analysis of intracellular proteins and subcellular localization using cellprofiler and imageJ in combination. . 2022-07-00. Pubmed ID: 33915291; DOI: 10.1016/j.ymeth.2021.04.019 KEIUi001-A 2022-07-00 2022-07-00 PubMed: 33915291 DOI: 10.1016/j.ymeth.2021.04.019Associated cell lines:
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Zhang J, Zhou T, Shan Y, Pan G
Generation of RYBP FLAG-HA knock-in human embryonic stem cell line through CRISPR/Cas9-mediated homologous recombination
Zhang J et al. Generation of RYBP FLAG-HA knock-in human embryonic stem cell line through CRISPR/Cas9-mediated homologous recombination. . 2022-07-00. Pubmed ID: 35537243; DOI: 10.1016/j.scr.2022.102803 WAe001-A-77 2022-07-00 2022-07-00 PubMed: 35537243 DOI: 10.1016/j.scr.2022.102803Associated cell lines:
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Wang D, Zhang R, Wang Y, Sun P, Ji X, Sun X, Xu J, Zhao D, Yan C, Liu F
Establishment of an induced pluripotent stem cell (iPSC) line (INNDSUi001-A) from a healthy female Chinese Han
Wang D et al. Establishment of an induced pluripotent stem cell (iPSC) line (INNDSUi001-A) from a healthy female Chinese Han. . 2022-07-00. Pubmed ID: 35636248; DOI: 10.1016/j.scr.2022.102819 INNDSUi001-A 2022-07-00 2022-07-00 PubMed: 35636248 DOI: 10.1016/j.scr.2022.102819Associated cell lines:
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de Jong S, Koolen L, Vázquez-Domínguez I, de Breuk A, Albert S, Hoyng CB, Katti S, den Hollander AI, Garanto A
Generation of an iPSC line (SCTCi015-A) and isogenic control line (SCTCi015-A-1) from an age-related macular degeneration patient carrying the variant c.355G>A in the CFI gene
de Jong S et al. Generation of an iPSC line (SCTCi015-A) and isogenic control line (SCTCi015-A-1) from an age-related macular degeneration patient carrying the variant c.355G>A in the CFI gene. . 2022-07-00. Pubmed ID: 35526389; DOI: 10.1016/j.scr.2022.102796 SCTCi015-ASCTCi015-A-1SCTCi016-A 2022-07-00 2022-07-00 PubMed: 35526389 DOI: 10.1016/j.scr.2022.102796Associated cell lines:
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Gulimiheranmu M, Li S, Zhou J
Generation of a MIR5004 knockout cell line from human induced pluripotent stem cells by CRISPR/Cas9 gene editing
Gulimiheranmu M et al. Generation of a MIR5004 knockout cell line from human induced pluripotent stem cells by CRISPR/Cas9 gene editing. . 2022-07-00. Pubmed ID: 35576811; DOI: 10.1016/j.scr.2022.102805 BJTTHi001-ASHCDCLi001-B 2022-07-00 2022-07-00 PubMed: 35576811 DOI: 10.1016/j.scr.2022.102805Associated cell lines:
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Moretti M, Limongi T, Testi C, Milanetti E, De Angelis MT, Parrotta EI, Scalise S, Santamaria G, Allione M, Lopatin S, Torre B, Zhang P, Marini M, Perozziello G, Candeloro P, Pirri CF, Ruocco G, Cuda G, Di Fabrizio E
Direct Visualization and Identification of Membrane Voltage-Gated Sodium Channels from Human iPSC-Derived Neurons by Multiple Imaging and Light Enhanced Spectroscopy
Moretti M et al. Direct Visualization and Identification of Membrane Voltage-Gated Sodium Channels from Human iPSC-Derived Neurons by Multiple Imaging and Light Enhanced Spectroscopy. . 2022-07-00. Pubmed ID: 35595684; DOI: 10.1002/smtd.202200402 UNIMGi003-AUNIMGi004-A 2022-07-00 2022-07-00 PubMed: 35595684 DOI: 10.1002/smtd.202200402Associated cell lines:
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Zhang D, Zhou M, Zhang Y, Shan Y, Pan G
Generation of an RNF1-deficient human pluripotent stem cell line using CRISPR/Cas9 technology
Zhang D et al. Generation of an RNF1-deficient human pluripotent stem cell line using CRISPR/Cas9 technology. . 2022-07-00. Pubmed ID: 35567848; DOI: 10.1016/j.scr.2022.102809 GIBHe013-A 2022-07-00 2022-07-00 PubMed: 35567848 DOI: 10.1016/j.scr.2022.102809Associated cell lines:
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Ababneh NA, Barham R, Al-Kurdi B, Ali D, Hadidi SA, A Ismail M, Muamar ASH, Abdulelah AA, Madadha A, Sallam M, Hassona Y, Masri A, Awidi A
Generation of a human induced pluripotent stem cell (iPSC) line (JUCTCi019-A) from a patient with Charcot-Marie-Tooth disease type 2A2 (CMT2A2) due to a heterozygous missense substitution c.2119C > T (p.Arg707Trp) in MFN2 gene
Ababneh NA et al. Generation of a human induced pluripotent stem cell (iPSC) line (JUCTCi019-A) from a patient with Charcot-Marie-Tooth disease type 2A2 (CMT2A2) due to a heterozygous missense substitution c.2119C > T (p.Arg707Trp) in MFN2 gene. . 2022-07-00. Pubmed ID: 35468369; DOI: 10.1016/j.scr.2022.102786 JUCTCi019-A 2022-07-00 2022-07-00 PubMed: 35468369 DOI: 10.1016/j.scr.2022.102786Associated cell lines:
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Supakul S, Leventoux N, Tabuchi H, Mimura M, Ito D, Maeda S, Okano H
Establishment of KEIOi005-A iPSC line from urine-derived cells (UDCs) of a mild Alzheimer's disease (AD) donor with multiple risk SNPs for sporadic Alzheimer's disease (sAD)
Supakul S et al. Establishment of KEIOi005-A iPSC line from urine-derived cells (UDCs) of a mild Alzheimer's disease (AD) donor with multiple risk SNPs for sporadic Alzheimer's disease (sAD). . 2022-07-00. Pubmed ID: 35537244; DOI: 10.1016/j.scr.2022.102802 KEIOi005-A 2022-07-00 2022-07-00 PubMed: 35537244 DOI: 10.1016/j.scr.2022.102802Associated cell lines:
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Luo X, Wang Y, Yuan F, Lin L, Wang A, Wang C, Guo M, Wang S, Wang C, Xu Q, Yin R, Cheng H, Zhang Y, Liu Z, Xu W, Yan J, Zeng F, Chen Y
Induced pluripotent stem cells (SHCDNi006-A cells) isolated from the peripheral blood mononuclear cells of a five-month-old Chinese girl with the heterozygous missense mutation (c.2800 G>A) in the KCNT1 gene
Luo X et al. Induced pluripotent stem cells (SHCDNi006-A cells) isolated from the peripheral blood mononuclear cells of a five-month-old Chinese girl with the heterozygous missense mutation (c.2800 G>A) in the KCNT1 gene. . 2022-07-00. Pubmed ID: 35537242; DOI: 10.1016/j.scr.2022.102798 SHCDNi006-A 2022-07-00 2022-07-00 PubMed: 35537242 DOI: 10.1016/j.scr.2022.102798Associated cell lines:
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Shimoda Y, Murakoshi N, Mori H, Xu D, Tajiri K, Hemmi Y, Sato I, Noguchi M, Nakamura Y, Hayashi Y, Ieda M
Generation of a human induced pluripotent stem cell line derived from a patient with dilated cardiomyopathy carrying LMNA nonsense mutation
Shimoda Y et al. Generation of a human induced pluripotent stem cell line derived from a patient with dilated cardiomyopathy carrying LMNA nonsense mutation. . 2022-07-00. Pubmed ID: 35500377; DOI: 10.1016/j.scr.2022.102793 BRCi021-A 2022-07-00 2022-07-00 PubMed: 35500377 DOI: 10.1016/j.scr.2022.102793Associated cell lines:
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Ji X, Wang Y, Sun P, Wang D, Sun X, Zhang R, Xu J, Li W, Liu F, Yan C
Generation of a human induced pluripotent stem cell line (INNDSUi003-A) derived from patient with Becker muscular dystrophy (BMD)
Ji X et al. Generation of a human induced pluripotent stem cell line (INNDSUi003-A) derived from patient with Becker muscular dystrophy (BMD). . 2022-07-00. Pubmed ID: 35526387; DOI: 10.1016/j.scr.2022.102794 INNDSUi003-A 2022-07-00 2022-07-00 PubMed: 35526387 DOI: 10.1016/j.scr.2022.102794Associated cell lines:
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Akter M, Cui H, Chen YH, Ding B
Generation of gene-corrected isogenic control cell lines from a DYT1 dystonia patient iPSC line carrying a heterozygous GAG mutation in TOR1A gene
Akter M et al. Generation of gene-corrected isogenic control cell lines from a DYT1 dystonia patient iPSC line carrying a heterozygous GAG mutation in TOR1A gene. . 2022-07-00. Pubmed ID: 35533513; DOI: 10.1016/j.scr.2022.102807; PMC: PMC9366766 CSUi002-ACSUi002-A-2CSUi002-A-3 2022-07-00 2022-07-00 PubMed: 35533513 DOI: 10.1016/j.scr.2022.102807Associated cell lines:
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Xu Q, Zhao T, Zhang Y, Fan W, Yan Y, Lan F
Generation of a human embryonic stem cell line (WAe009-A-78) carrying homozygous TBX18 knockout
Xu Q et al. Generation of a human embryonic stem cell line (WAe009-A-78) carrying homozygous TBX18 knockout. . 2022-07-00. Pubmed ID: 35533514; DOI: 10.1016/j.scr.2022.102804 WAe009-AWAe009-A-78 2022-07-00 2022-07-00 PubMed: 35533514 DOI: 10.1016/j.scr.2022.102804Associated cell lines:
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Lager TW, Zuo J, Alam MS, Calhoun B, Haldar K, Panopoulos AD
Generation of three induced pluripotent stem cell lines from a patient with Kabuki syndrome carrying the KMT2D p.R4198X mutation
Lager TW et al. Generation of three induced pluripotent stem cell lines from a patient with Kabuki syndrome carrying the KMT2D p.R4198X mutation. . 2022-07-00. Pubmed ID: 35550987; DOI: 10.1016/j.scr.2022.102799 NDi004-ANDi004-BNDi004-C 2022-07-00 2022-07-00 PubMed: 35550987 DOI: 10.1016/j.scr.2022.102799 -
Fang S, Zeng A, Xu Q, Zhou L, Zhang Z, An Y, Zhao X
Generation of human induced pluripotent stem cell line from peripheral blood mononuclear cells from an activated phosphoinositide 3-kinase δ syndrome patient
Fang S et al. Generation of human induced pluripotent stem cell line from peripheral blood mononuclear cells from an activated phosphoinositide 3-kinase δ syndrome patient. . 2022-07-00. Pubmed ID: 35660815; DOI: 10.1016/j.scr.2022.102822 CHCMUi001-A 2022-07-00 2022-07-00 PubMed: 35660815 DOI: 10.1016/j.scr.2022.102822Associated cell lines:
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Bashirzade AA, Zabegalov KN, Volgin AD, Belova AS, Demin KA, de Abreu MS, Babchenko VY, Bashirzade KA, Yenkoyan KB, Tikhonova MA, Amstislavskaya TG, Kalueff AV
Modeling neurodegenerative disorders in zebrafish
Bashirzade AA et al. Modeling neurodegenerative disorders in zebrafish. . 2022-07-00. Pubmed ID: 35490912; DOI: 10.1016/j.neubiorev.2022.104679 HIHDNDi001-AHIHDNDi001-B 2022-07-00 2022-07-00 PubMed: 35490912 DOI: 10.1016/j.neubiorev.2022.104679Associated cell lines:
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Hoppe B, Martin-Higueras C
Improving Treatment Options for Primary Hyperoxaluria
Hoppe B et al. Improving Treatment Options for Primary Hyperoxaluria. . 2022-07-00. Pubmed ID: 35779234; DOI: 10.1007/s40265-022-01735-x; PMC: PMC9329168 CIMAi001-A 2022-07-00 2022-07-00 PubMed: 35779234 DOI: 10.1007/s40265-022-01735-xAssociated cell lines:
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Chen CX, You Z, Abdian N, Sirois J, Shlaifer I, Tabatabaei M, Boivin MN, Gaborieau L, Karamchandani J, Beitel LK, Fon EA, Durcan TM
Generation of homozygous PRKN, PINK1 and double PINK1/PRKN knockout cell lines from healthy induced pluripotent stem cells using CRISPR/Cas9 editing
Chen CX et al. Generation of homozygous PRKN, PINK1 and double PINK1/PRKN knockout cell lines from healthy induced pluripotent stem cells using CRISPR/Cas9 editing. . 2022-07-00. Pubmed ID: 35561458; DOI: 10.1016/j.scr.2022.102806 CBIGi001-ACBIGi001-A-1CBIGi001-A-2CBIGi001-A-3 2022-07-00 2022-07-00 PubMed: 35561458 DOI: 10.1016/j.scr.2022.102806Associated cell lines:
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Wang Q, Zhang Y, Zhang F, Li Z, Cheng H, Lin Y, Zhu Y, Chen H, Cui C, Chen M
Generation of a human induced pluripotent stem cell line (JSPHi002-A) from a patient with long-QT syndrome type 1 caused by KCNQ1 c.773A > T mutation
Wang Q et al. Generation of a human induced pluripotent stem cell line (JSPHi002-A) from a patient with long-QT syndrome type 1 caused by KCNQ1 c.773A > T mutation. . 2022-07-00. Pubmed ID: 35580545; DOI: 10.1016/j.scr.2022.102810 JSPHi002-A 2022-07-00 2022-07-00 PubMed: 35580545 DOI: 10.1016/j.scr.2022.102810Associated cell lines:
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Jimenez-Vazquez EN, Arad M, Macías Á, Vera-Pedrosa ML, Cruz FM, Gutierrez LK, Cuttitta AJ, Monteiro da Rocha A, Herron TJ, Ponce-Balbuena D, Guerrero-Serna G, Binah O, Michele DE, Jalife J
SNTA1 gene rescues ion channel function and is antiarrhythmic in cardiomyocytes derived from induced pluripotent stem cells from muscular dystrophy patients
Jimenez-Vazquez EN et al. SNTA1 gene rescues ion channel function and is antiarrhythmic in cardiomyocytes derived from induced pluripotent stem cells from muscular dystrophy patients. . 2022-06-28. Pubmed ID: 35762211; DOI: 10.7554/elife.76576; PMC: PMC9239678 IITi001-A 2022-06-28 2022-06-28 PubMed: 35762211 DOI: 10.7554/elife.76576Associated cell lines:
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Xiaoyu L.
Bardet-Biedl syndrome in a female due to a novel compound heterozygous mutations in BBS10 gene: One case report and literature review
Xiaoyu L.. Bardet-Biedl syndrome in a female due to a novel compound heterozygous mutations in BBS10 gene: One case report and literature review. . 2022-06-25. DOI: 10.3760/cma.j.cn311282-20201222-00845 KCi002-A 2022-06-25 2022-06-25 DOI: 10.3760/cma.j.cn311282-20201222-00845Associated cell lines:
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Chou PC, Liu CM, Weng CH, Yang KC, Cheng ML, Lin YC, Yang RB, Shyu BC, Shyue SK, Liu JD, Chen SP, Hsiao M, Hu YF
Fibroblasts Drive Metabolic Reprogramming in Pacemaker Cardiomyocytes
Chou PC et al. Fibroblasts Drive Metabolic Reprogramming in Pacemaker Cardiomyocytes. . 2022-06-24. Pubmed ID: 35611699; DOI: 10.1161/circresaha.121.320301 IBMSi013-AIBMSi014-AIBMSi015-AIBMSi016-AIBMSi017-AIBMSi018-A 2022-06-24 2022-06-24 PubMed: 35611699 DOI: 10.1161/circresaha.121.320301Associated cell lines:
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Zhang Y, Duan X
A Novel 90-kbp Deletion of RUNX2 Associated with Cleidocranial Dysplasia
Zhang Y et al. A Novel 90-kbp Deletion of RUNX2 Associated with Cleidocranial Dysplasia. . 2022-06-23. Pubmed ID: 35885911; DOI: 10.3390/genes13071128; PMC: PMC9322484 GZHMCi003-A 2022-06-23 2022-06-23 PubMed: 35885911 DOI: 10.3390/genes13071128Associated cell lines:
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Molina-Ruiz FJ, Introna C, Bombau G, Galofre M, Canals JM
Standardization of Cell Culture Conditions and Routine Genomic Screening under a Quality Management System Leads to Reduced Genomic Instability in hPSCs
Molina-Ruiz FJ et al. Standardization of Cell Culture Conditions and Routine Genomic Screening under a Quality Management System Leads to Reduced Genomic Instability in hPSCs. . 2022-06-21. Pubmed ID: 35805069; DOI: 10.3390/cells11131984; PMC: PMC9265327 WAe009-AGENEAe015-AGENEAe020-ARUESe002-ARUESe002-A-1CHDIi010-ACHDIi013-ACHDIi014-ACHDIi016-ACHDIi022-ACHDIi026-ACHDIi027-ACHDIi042-ACHDIi049-ARUESe002-A-2 2022-06-21 2022-06-21 PubMed: 35805069 DOI: 10.3390/cells11131984 -
Rohde F, Danz K, Jung N, Wagner S, Windbergs M
Electrospun Scaffolds as Cell Culture Substrates for the Cultivation of an In Vitro Blood-Brain Barrier Model Using Human Induced Pluripotent Stem Cells
Rohde F et al. Electrospun Scaffolds as Cell Culture Substrates for the Cultivation of an In Vitro Blood-Brain Barrier Model Using Human Induced Pluripotent Stem Cells. . 2022-06-20. Pubmed ID: 35745880; DOI: 10.3390/pharmaceutics14061308; PMC: PMC9231001 UKKi011-A 2022-06-20 2022-06-20 PubMed: 35745880 DOI: 10.3390/pharmaceutics14061308Associated cell lines:
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Närvä E, Taskinen ME, Lilla S, Isomursu A, Pietilä M, Weltner J, Isola J, Sihto H, Joensuu H, Zanivan S, Norman J, Ivaska J
MASTL is enriched in cancerous and pluripotent stem cells and influences OCT1/OCT4 levels
Närvä E et al. MASTL is enriched in cancerous and pluripotent stem cells and influences OCT1/OCT4 levels. . 2022-06-17. Pubmed ID: 35677646; DOI: 10.1016/j.isci.2022.104459; PMC: PMC9167974 UHi007-BUHi020-A 2022-06-17 2022-06-17 PubMed: 35677646 DOI: 10.1016/j.isci.2022.104459 -
Bruge C, Geoffroy M, Benabides M, Pellier E, Gicquel E, Dhiab J, Hoch L, Richard I, Nissan X
Skeletal Muscle Cells Derived from Induced Pluripotent Stem Cells: A Platform for Limb Girdle Muscular Dystrophies
Bruge C et al. Skeletal Muscle Cells Derived from Induced Pluripotent Stem Cells: A Platform for Limb Girdle Muscular Dystrophies. . 2022-06-16. Pubmed ID: 35740450; DOI: 10.3390/biomedicines10061428; PMC: PMC9220148 CSCRMi001-A 2022-06-16 2022-06-16 PubMed: 35740450 DOI: 10.3390/biomedicines10061428Associated cell lines:
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Ullah MI
Clinical and Mutation Spectrum of Autosomal Recessive Non-Syndromic Oculocutaneous Albinism (nsOCA) in Pakistan: A Review
Ullah MI. Clinical and Mutation Spectrum of Autosomal Recessive Non-Syndromic Oculocutaneous Albinism (nsOCA) in Pakistan: A Review. . 2022-06-16. Pubmed ID: 35741834; DOI: 10.3390/genes13061072; PMC: PMC9222488 SEIi001-A 2022-06-16 2022-06-16 PubMed: 35741834 DOI: 10.3390/genes13061072Associated cell lines:
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Ma C, Jin K, Jin ZB
Generation of Human Patient iPSC-derived Retinal Organoids to Model Retinitis Pigmentosa
Ma C et al. Generation of Human Patient iPSC-derived Retinal Organoids to Model Retinitis Pigmentosa. . 2022-06-16. Pubmed ID: 35786611; DOI: 10.3791/64045 BIOi002-A 2022-06-16 2022-06-16 PubMed: 35786611 DOI: 10.3791/64045Associated cell lines:
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Jäntti H, Sitnikova V, Ishchenko Y, Shakirzyanova A, Giudice L, Ugidos IF, Gómez-Budia M, Korvenlaita N, Ohtonen S, Belaya I, Fazaludeen F, Mikhailov N, Gotkiewicz M, Ketola K, Lehtonen Š, Koistinaho J, Kanninen KM, Hernández D, Pébay A, Giugno R, Korhonen P, Giniatullin R, Malm T
Microglial amyloid beta clearance is driven by PIEZO1 channels
Jäntti H et al. Microglial amyloid beta clearance is driven by PIEZO1 channels. . 2022-06-15. Pubmed ID: 35706029; DOI: 10.1186/s12974-022-02486-y; PMC: PMC9199162 BIONi010-CBIONi010-C-2 2022-06-15 2022-06-15 PubMed: 35706029 DOI: 10.1186/s12974-022-02486-yAssociated cell lines:
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Ramovs V, Janssen H, Fuentes I, Pitaval A, Rachidi W, Chuva de Sousa Lopes SM, Freund C, Gidrol X, Mummery CL, Raymond K
Characterization of the epidermal-dermal junction in hiPSC-derived skin organoids
Ramovs V et al. Characterization of the epidermal-dermal junction in hiPSC-derived skin organoids. . 2022-06-14. Pubmed ID: 35561682; DOI: 10.1016/j.stemcr.2022.04.008; PMC: PMC9213820 LUMCi045-ALUMCi046-A 2022-06-14 2022-06-14 PubMed: 35561682 DOI: 10.1016/j.stemcr.2022.04.008Associated cell lines:
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Rahman MU, Bilal M, Shah JA, Kaushik A, Teissedre PL, Kujawska M
CRISPR-Cas9-Based Technology and Its Relevance to Gene Editing in Parkinson's Disease
Rahman MU et al. CRISPR-Cas9-Based Technology and Its Relevance to Gene Editing in Parkinson's Disease. . 2022-06-13. Pubmed ID: 35745824; DOI: 10.3390/pharmaceutics14061252; PMC: PMC9229276 KEIUi001-A 2022-06-13 2022-06-13 PubMed: 35745824 DOI: 10.3390/pharmaceutics14061252Associated cell lines:
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Daniszewski M, Senabouth A, Liang HH, Han X, Lidgerwood GE, Hernández D, Sivakumaran P, Clarke JE, Lim SY, Lees JG, Rooney L, Gulluyan L, Souzeau E, Graham SL, Chan CL, Nguyen U, Farbehi N, Gnanasambandapillai V, McCloy RA, Clarke L, Kearns LS, Mackey DA, Craig JE, MacGregor S, Powell JE, Pébay A, Hewitt AW
Retinal ganglion cell-specific genetic regulation in primary open-angle glaucoma
Daniszewski M et al. Retinal ganglion cell-specific genetic regulation in primary open-angle glaucoma. . 2022-06-08. Pubmed ID: 36778138; DOI: 10.1016/j.xgen.2022.100142; PMC: PMC9903700 UOMELBi001-A 2022-06-08 2022-06-08 PubMed: 36778138 DOI: 10.1016/j.xgen.2022.100142Associated cell lines:
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Aguilar-González A, González-Correa JE, Barriocanal-Casado E, Ramos-Hernández I, Lerma-Juárez MA, Greco S, Rodríguez-Sevilla JJ, Molina-Estévez FJ, Montalvo-Romeral V, Ronzitti G, Sánchez-Martín RM, Martín F, Muñoz P
Isogenic GAA-KO Murine Muscle Cell Lines Mimicking Severe Pompe Mutations as Preclinical Models for the Screening of Potential Gene Therapy Strategies
Aguilar-González A et al. Isogenic GAA-KO Murine Muscle Cell Lines Mimicking Severe Pompe Mutations as Preclinical Models for the Screening of Potential Gene Therapy Strategies. . 2022-06-04. Pubmed ID: 35682977; DOI: 10.3390/ijms23116298; PMC: PMC9181599 TRNDi007-B 2022-06-04 2022-06-04 PubMed: 35682977 DOI: 10.3390/ijms23116298Associated cell lines:
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Li J, Feng X, Wei X
Modeling hypertrophic cardiomyopathy with human cardiomyocytes derived from induced pluripotent stem cells
Li J et al. Modeling hypertrophic cardiomyopathy with human cardiomyocytes derived from induced pluripotent stem cells. . 2022-06-03. Pubmed ID: 35659761; DOI: 10.1186/s13287-022-02905-0; PMC: PMC9166443 EHTJUi003-A 2022-06-03 2022-06-03 PubMed: 35659761 DOI: 10.1186/s13287-022-02905-0Associated cell lines:
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Jetten AM, Scoville DW, Kang HS
GLIS1-3: Links to Primary Cilium, Reprogramming, Stem Cell Renewal, and Disease
Jetten AM et al. GLIS1-3: Links to Primary Cilium, Reprogramming, Stem Cell Renewal, and Disease. . 2022-06-03. Pubmed ID: 35681527; DOI: 10.3390/cells11111833; PMC: PMC9180737 RCMGi004-A 2022-06-03 2022-06-03 PubMed: 35681527 DOI: 10.3390/cells11111833Associated cell lines:
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Cnossen MH, van Moort I, Reitsma SH, de Maat MPM, Schutgens REG, Urbanus RT, Lingsma HF, Mathot RAA, Gouw SC, Meijer K, Bredenoord AL, van der Graaf R, Fijnvandraat K, Meijer AB, van den Akker E, Bierings R, Eikenboom JCJ, van den Biggelaar M, de Haas M, Voorberg J, Leebeek FWG, SYMPHONY consortium
SYMPHONY consortium: Orchestrating personalized treatment for patients with bleeding disorders
Cnossen MH et al. SYMPHONY consortium: Orchestrating personalized treatment for patients with bleeding disorders. . 2022-06-02. Pubmed ID: 35652368; DOI: 10.1111/jth.15778; PMC: PMC9545335 SANi005-ASANi006-A 2022-06-02 2022-06-02 PubMed: 35652368 DOI: 10.1111/jth.15778 -
Long P, Shi Y, Sun F, Wei Y, Wu B, Li Q, Jie Q, Ma Y
Establishment of a non-integrated induced pluripotent stem cell line derived from human chorionic villi cells
Long P et al. Establishment of a non-integrated induced pluripotent stem cell line derived from human chorionic villi cells. . 2022-06-00. Pubmed ID: 35527669; DOI: 10.1002/jcla.24464; PMC: PMC9169189 ZZUi008-A 2022-06-00 2022-06-00 PubMed: 35527669 DOI: 10.1002/jcla.24464Associated cell lines:
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Rosebrock D, Arora S, Mutukula N, Volkman R, Gralinska E, Balaskas A, Aragonés Hernández A, Buschow R, Brändl B, Müller FJ, Arndt PF, Vingron M, Elkabetz Y
Enhanced cortical neural stem cell identity through short SMAD and WNT inhibition in human cerebral organoids facilitates emergence of outer radial glial cells
Rosebrock D et al. Enhanced cortical neural stem cell identity through short SMAD and WNT inhibition in human cerebral organoids facilitates emergence of outer radial glial cells. . 2022-06-00. Pubmed ID: 35697781; DOI: 10.1038/s41556-022-00929-5; PMC: PMC9203281 MPIPi008-A 2022-06-00 2022-06-00 PubMed: 35697781 DOI: 10.1038/s41556-022-00929-5Associated cell lines:
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Ishi Y, Era T, Yuzawa S, Okamoto M, Sawaya R, Motegi H, Yamaguchi S, Terasaka S, Houkin K, Fujimura M
Analysis of induced pluripotent stem cell clones derived from a patient with mosaic neurofibromatosis type 2
Ishi Y et al. Analysis of induced pluripotent stem cell clones derived from a patient with mosaic neurofibromatosis type 2. . 2022-06-00. Pubmed ID: 35178855; DOI: 10.1002/ajmg.a.62700 KAUSTi006-AKAUSTi006-B 2022-06-00 2022-06-00 PubMed: 35178855 DOI: 10.1002/ajmg.a.62700Associated cell lines:
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Khedro T, Duran JM, Adler ED
Modeling Nonischemic Genetic Cardiomyopathies Using Induced Pluripotent Stem Cells
Khedro T et al. Modeling Nonischemic Genetic Cardiomyopathies Using Induced Pluripotent Stem Cells. . 2022-06-00. Pubmed ID: 35657495; DOI: 10.1007/s11886-022-01683-8; PMC: PMC9164178 HDZi001-A 2022-06-00 2022-06-00 PubMed: 35657495 DOI: 10.1007/s11886-022-01683-8Associated cell lines:
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Ateaque S, Merkouris S, Wyatt S, Allen ND, Xie J, DiStefano PS, Lindsay RM, Barde YA
Selective activation and down-regulation of Trk receptors by neurotrophins in human neurons co-expressing TrkB and TrkC
Ateaque S et al. Selective activation and down-regulation of Trk receptors by neurotrophins in human neurons co-expressing TrkB and TrkC. . 2022-06-00. Pubmed ID: 35536742; DOI: 10.1111/jnc.15617; PMC: PMC9321069 WAe009-A 2022-06-00 2022-06-00 PubMed: 35536742 DOI: 10.1111/jnc.15617Associated cell lines:
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Aguillon D, Vasquez D, Madrigal L, Moreno S, Hernández D, Isaza-Ruget M, Lopez JJ, Landires I, Nuñez-Samudio V, Restrepo CM, Vidal OM, Vélez JI, Arcos-Holzinger M, Lopera F, Arcos-Burgos M
Ataxia with Ocular Apraxia Type 1 (AOA1) (APTX, W279* Mutation): Neurological, Neuropsychological, and Molecular Outlining of a Heterogenous Phenotype in Four Colombian Siblings
Aguillon D et al. Ataxia with Ocular Apraxia Type 1 (AOA1) (APTX, W279* Mutation): Neurological, Neuropsychological, and Molecular Outlining of a Heterogenous Phenotype in Four Colombian Siblings. . 2022-06-00. Pubmed ID: 35420381; DOI: 10.1007/s12035-022-02821-7 JUCTCi002-A 2022-06-00 2022-06-00 PubMed: 35420381 DOI: 10.1007/s12035-022-02821-7Associated cell lines:
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Torriano S, Baulier E, Garcia Diaz A, Corneo B, Farber DB
CRISPR-AsCas12a Efficiently Corrects a GPR143 Intronic Mutation in Induced Pluripotent Stem Cells from an Ocular Albinism Patient
Torriano S et al. CRISPR-AsCas12a Efficiently Corrects a GPR143 Intronic Mutation in Induced Pluripotent Stem Cells from an Ocular Albinism Patient. . 2022-06-00. Pubmed ID: 35686978; DOI: 10.1089/crispr.2021.0110; PMC: PMC9233509 SEIi001-A 2022-06-00 2022-06-00 PubMed: 35686978 DOI: 10.1089/crispr.2021.0110Associated cell lines:
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Pollara L, Sottile V, Valente EM
Patient-derived cellular models of primary ciliopathies
Pollara L et al. Patient-derived cellular models of primary ciliopathies. . 2022-06-00. Pubmed ID: 35184035; DOI: 10.1136/jmedgenet-2021-108315 CSSi007-A 2022-06-00 2022-06-00 PubMed: 35184035 DOI: 10.1136/jmedgenet-2021-108315Associated cell lines:
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Ejlersen M, Ilieva M, Michel TM
Superoxide dismutase isozymes in cerebral organoids from autism spectrum disorder patients
Ejlersen M et al. Superoxide dismutase isozymes in cerebral organoids from autism spectrum disorder patients. . 2022-06-00. Pubmed ID: 35266053; DOI: 10.1007/s00702-022-02472-x SDUKIi002-ASDUKIi003-ASDUKIi004-ASDUKIi006-A 2022-06-00 2022-06-00 PubMed: 35266053 DOI: 10.1007/s00702-022-02472-xAssociated cell lines:
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Petrus-Reurer Sandra, Lederer Alex R., Baqué-Vidal Laura, Douagi Iyadh, Pannagel Belinda, Khven Irina, Aronsson Monica, Bartuma Hammurabi, Wagner Magdalena, Wrona Andreas, Efstathopoulos Paschalis, Jaberi Elham, Willenbrock Hanni, Shimizu Yutaka, Villaescusa J. Carlos, André Helder, Sundstrӧm Erik, Bhaduri Aparna, Kriegstein Arnold, Kvanta Anders, La Manno Gioele, Lanner Fredrik
Molecular profiling of stem cell-derived retinal pigment epithelial cell differentiation established for clinical translation
Petrus-Reurer Sandra et al. Molecular profiling of stem cell-derived retinal pigment epithelial cell differentiation established for clinical translation. . 2022-06-00. DOI: 10.1016/j.stemcr.2022.05.005 NOVOe002-A 2022-06-00 2022-06-00 DOI: 10.1016/j.stemcr.2022.05.005Associated cell lines:
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Jellinger KA
Pallidal degenerations and related disorders: an update
Jellinger KA. Pallidal degenerations and related disorders: an update. . 2022-06-00. Pubmed ID: 34363531; DOI: 10.1007/s00702-021-02392-2 CSSi008-A 2022-06-00 2022-06-00 PubMed: 34363531 DOI: 10.1007/s00702-021-02392-2Associated cell lines:
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Dos Santos T, Galipeau M, Schukarucha Gomes A, Greenberg M, Larsen M, Lee D, Maghera J, Mulchandani CM, Patton M, Perera I, Polishevska K, Ramdass S, Shayeganpour K, Vafaeian K, Van Allen K, Wang Y, Weisz T, Estall JL, Mulvihill EE, Screaton RA, Diabetes Action Canada and the Canadian Islet Research and Training Network
Islet Biology During COVID-19: Progress and Perspectives
Dos Santos T et al. Islet Biology During COVID-19: Progress and Perspectives. . 2022-06-00. Pubmed ID: 35589534; DOI: 10.1016/j.jcjd.2021.11.002; PMC: PMC8608413 WAe001-AWAe001-A-12 2022-06-00 2022-06-00 PubMed: 35589534 DOI: 10.1016/j.jcjd.2021.11.002Associated cell lines:
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Zawada Dorota, Kornherr Jessica, Meier Anna B., Santamaria Gianluca, Dorn Tatjana, Ortmann Daniel, Lachmann Mark, Ortiz Mariaestela, Harmer Stephen C., Nobles Muriel, Tinker Andrew, Pedersen Roger A., Grote Phillip, Laugwitz Karl-Ludwig, Moretti Alessandra, Goedel Alexander
Retinoic acid signaling modulation guides in vitro specification of human heart field-specific progenitor pools
Zawada Dorota et al. Retinoic acid signaling modulation guides in vitro specification of human heart field-specific progenitor pools. . 2022-05-30. DOI: 10.1101/2022.05.30.494027 MRIi003-AMRIi020-A 2022-05-30 2022-05-30 DOI: 10.1101/2022.05.30.494027 -
Vanslambrouck JM, Wilson SB, Tan KS, Groenewegen E, Rudraraju R, Neil J, Lawlor KT, Mah S, Scurr M, Howden SE, Subbarao K, Little MH
Enhanced metanephric specification to functional proximal tubule enables toxicity screening and infectious disease modelling in kidney organoids
Vanslambrouck JM et al. Enhanced metanephric specification to functional proximal tubule enables toxicity screening and infectious disease modelling in kidney organoids. . 2022-05-27. Pubmed ID: 35665006; DOI: 10.1101/2021.10.14.464320; PMC: PMC9164445 MCRIi010-A 2022-05-27 2022-05-27 PubMed: 35665006 DOI: 10.1101/2021.10.14.464320Associated cell lines:
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Ustyantseva E, Pavlova SV, Malakhova AA, Ustyantsev K, Zakian SM, Medvedev SP
Oxidative stress monitoring in iPSC-derived motor neurons using genetically encoded biosensors of H(2)O(2)
Ustyantseva E et al. Oxidative stress monitoring in iPSC-derived motor neurons using genetically encoded biosensors of H(2)O(2). . 2022-05-27. Pubmed ID: 35624228; DOI: 10.1038/s41598-022-12807-z; PMC: PMC9142597 ICGi014-AICGi021-AICGi022-A 2022-05-27 2022-05-27 PubMed: 35624228 DOI: 10.1038/s41598-022-12807-z -
Maretina Marianna A., Kiselev Anton V., Ilina Arina V., Egorova Anna A., Glotov Andrey S., Bespalova Olesya N., Baranov Vladislav S., Kogan Igor Yu.
Current Trends in the Diagnosis, Screening and Treatment of Spinal Muscular Atrophy
Maretina Marianna A. et al. Current Trends in the Diagnosis, Screening and Treatment of Spinal Muscular Atrophy. . 2022-05-26. DOI: 10.15690/vramn1768 ICGi003-A 2022-05-26 2022-05-26 DOI: 10.15690/vramn1768Associated cell lines:
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Varga BV, Faiz M, Pivonkova H, Khelifi G, Yang H, Gao S, Linderoth E, Zhen M, Karadottir RT, Hussein SM, Nagy A
Signal requirement for cortical potential of transplantable human neuroepithelial stem cells
Varga BV et al. Signal requirement for cortical potential of transplantable human neuroepithelial stem cells. . 2022-05-23. Pubmed ID: 35606347; DOI: 10.1038/s41467-022-29839-8; PMC: PMC9126949 WAe001-AWAe009-A 2022-05-23 2022-05-23 PubMed: 35606347 DOI: 10.1038/s41467-022-29839-8 -
Wei Jingzhang, Arber Charles, Wray Selina, Hardy John, Piers Thomas M, Pocock Jennifer M
Glucocorticoid receptor activation during human microglial differentiation leads to genomic instability and senescence
Wei Jingzhang et al. Glucocorticoid receptor activation during human microglial differentiation leads to genomic instability and senescence. . 2022-05-23. DOI: 10.1101/2022.05.23.493044 BIONi010-C 2022-05-23 2022-05-23 DOI: 10.1101/2022.05.23.493044Associated cell lines:
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Metzler E, Escobar H, Sunaga-Franze DY, Sauer S, Diecke S, Spuler S
Generation of hiPSC-Derived Skeletal Muscle Cells: Exploiting the Potential of Skeletal Muscle-Derived hiPSCs
Metzler E et al. Generation of hiPSC-Derived Skeletal Muscle Cells: Exploiting the Potential of Skeletal Muscle-Derived hiPSCs. . 2022-05-23. Pubmed ID: 35625941; DOI: 10.3390/biomedicines10051204; PMC: PMC9138862 MDCi011-AMDCi011-BMDCi012-AMDCi012-BMDCi013-AMDCi013-BMDCi014-AMDCi014-B 2022-05-23 2022-05-23 PubMed: 35625941 DOI: 10.3390/biomedicines10051204 -
Duclaux-Loras R, Lebreton C, Berthelet J, Charbit-Henrion F, Nicolle O, Revenu des Courtils C, Waich S, Valovka T, Khiat A, Rabant M, Racine C, Guerrera IC, Baptista J, Mahe MM, Hess MW, Durel B, Lefort N, Banal C, Parisot M, Talbotec C, Lacaille F, Ecochard-Dugelay E, Demir AM, Vogel GF, Faivre L, Rodrigues A, Fowler D, Janecke AR, Müller T, Huber LA, Rodrigues-Lima F, Ruemmele FM, Uhlig HH, Del Bene F, Michaux G, Cerf-Bensussan N, Parlato M
UNC45A deficiency causes microvillus inclusion disease-like phenotype by impairing myosin VB-dependent apical trafficking
Duclaux-Loras R et al. UNC45A deficiency causes microvillus inclusion disease-like phenotype by impairing myosin VB-dependent apical trafficking. . 2022-05-16. Pubmed ID: 35575086; DOI: 10.1172/jci154997; PMC: PMC9106349 IMAGINi020-A 2022-05-16 2022-05-16 PubMed: 35575086 DOI: 10.1172/jci154997Associated cell lines:
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Ajayi PT, Katti P, Zhang Y, Willingham TB, Sun Y, Bleck CKE, Glancy B
Regulation of the evolutionarily conserved muscle myofibrillar matrix by cell type dependent and independent mechanisms
Ajayi PT et al. Regulation of the evolutionarily conserved muscle myofibrillar matrix by cell type dependent and independent mechanisms. . 2022-05-13. Pubmed ID: 35562354; DOI: 10.1038/s41467-022-30401-9; PMC: PMC9106682 KICRi002-AKICRi002-A-3 2022-05-13 2022-05-13 PubMed: 35562354 DOI: 10.1038/s41467-022-30401-9Associated cell lines:
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Lyu Y, Jia W, Wu Y, Zhao X, Xia Y, Guo X, Kang J
Cpmer: A new conserved eEF1A2-binding partner that regulates Eomes translation and cardiomyocyte differentiation
Lyu Y et al. Cpmer: A new conserved eEF1A2-binding partner that regulates Eomes translation and cardiomyocyte differentiation. . 2022-05-10. Pubmed ID: 35395174; DOI: 10.1016/j.stemcr.2022.03.006; PMC: PMC9133893 WAe009-A 2022-05-10 2022-05-10 PubMed: 35395174 DOI: 10.1016/j.stemcr.2022.03.006Associated cell lines:
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Linn AK, Maneepitasut W, Tubsuwan A, Kitiyanant N, Phakdeekitcharoen B, Borwornpinyo S, Hongeng S, Phanthong P
Establishment and Characterization of MUi027-A: A Novel Patient-Derived Cell Line of Polycystic Kidney Disease with PKD1 Mutation
Linn AK et al. Establishment and Characterization of MUi027-A: A Novel Patient-Derived Cell Line of Polycystic Kidney Disease with PKD1 Mutation. . 2022-05-09. Pubmed ID: 35629189; DOI: 10.3390/jpm12050766; PMC: PMC9145395 MUi019-AMUi026-AMUi027-A 2022-05-09 2022-05-09 PubMed: 35629189 DOI: 10.3390/jpm12050766 -
Scalise S, Zannino C, Lucchino V, Lo Conte M, Scaramuzzino L, Cifelli P, D'Andrea T, Martinello K, Fucile S, Palma E, Gambardella A, Ruffolo G, Cuda G, Parrotta EI
Human iPSC Modeling of Genetic Febrile Seizure Reveals Aberrant Molecular and Physiological Features Underlying an Impaired Neuronal Activity
Scalise S et al. Human iPSC Modeling of Genetic Febrile Seizure Reveals Aberrant Molecular and Physiological Features Underlying an Impaired Neuronal Activity. . 2022-05-05. Pubmed ID: 35625812; DOI: 10.3390/biomedicines10051075; PMC: PMC9138645 UNIMGi001-AUNIMGi003-AUNIMGi004-A 2022-05-05 2022-05-05 PubMed: 35625812 DOI: 10.3390/biomedicines10051075Associated cell lines:
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Steinke Stephan, Kirmann Toni, Nerlich Jana, Weichard Iron, Kuhn Philip, Bullmann Torsten, Ritzau-Jost Andreas, Rizalar Filiz Sila, Prüss Harald, Haucke Volker, Geis Christian, Hust Michael, Hallermann Stefan
NMDA-receptor-Fc-fusion constructs neutralize anti-NMDA receptor antibodies
Steinke Stephan et al. NMDA-receptor-Fc-fusion constructs neutralize anti-NMDA receptor antibodies. . 2022-05-01. DOI: 10.1101/2022.04.29.490085 BIHi005-A-24 2022-05-01 2022-05-01 DOI: 10.1101/2022.04.29.490085Associated cell lines:
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Liu YQ, Ling TW, Wang HY, Yang YH, Song WJ, Wang TC
Generation of an integration-free induced pluripotent stem cell line (LZUSHI001-A) from an epileptic patient with DGKG mutation
Liu YQ et al. Generation of an integration-free induced pluripotent stem cell line (LZUSHI001-A) from an epileptic patient with DGKG mutation. . 2022-05-00. Pubmed ID: 35421845; DOI: 10.1016/j.scr.2022.102768 LZUSHi001-A 2022-05-00 2022-05-00 PubMed: 35421845 DOI: 10.1016/j.scr.2022.102768Associated cell lines:
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Wu H, Fang J, Liu Y, Wang J, Chen Z, Wang J, Shi H
Generation of an integration-free induced pluripotent stem cell line (JTUi004-A) from an otosclerosis patient
Wu H et al. Generation of an integration-free induced pluripotent stem cell line (JTUi004-A) from an otosclerosis patient. . 2022-05-00. Pubmed ID: 35413565; DOI: 10.1016/j.scr.2022.102783 JTUi002-AJTUi004-A 2022-05-00 2022-05-00 PubMed: 35413565 DOI: 10.1016/j.scr.2022.102783 -
Wang C, Yuan C, Ji Z, Yin J, Zhang Z, Zhang H, Zheng B, Zhou W, Yang S
Generation of patient-derived IPSC lines from a girl with Combined Oxidative Phosphorylation Deficiency 23 (COXPD23) caused by compound heterozygous GTPBP3 variants
Wang C et al. Generation of patient-derived IPSC lines from a girl with Combined Oxidative Phosphorylation Deficiency 23 (COXPD23) caused by compound heterozygous GTPBP3 variants. . 2022-05-00. Pubmed ID: 35413567; DOI: 10.1016/j.scr.2022.102775 DPNJMUi001-A 2022-05-00 2022-05-00 PubMed: 35413567 DOI: 10.1016/j.scr.2022.102775Associated cell lines:
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Yinghong Y, Qian L, Bing S, Yingjun X, Wenzhi H, Bangzhu C, Xiaofang S
Generation of two induced pluripotent stem cell lines, GZHMCi009-A and GZHMCi010-A, derived from peripheral blood mononuclear cells of two SCA3 patients with 14/74 CAG repeats of the ATXN3 mutation
Yinghong Y et al. Generation of two induced pluripotent stem cell lines, GZHMCi009-A and GZHMCi010-A, derived from peripheral blood mononuclear cells of two SCA3 patients with 14/74 CAG repeats of the ATXN3 mutation. . 2022-05-00. Pubmed ID: 35421843; DOI: 10.1016/j.scr.2022.102782 GZHMCi009-AGZHMCi010-A 2022-05-00 2022-05-00 PubMed: 35421843 DOI: 10.1016/j.scr.2022.102782Associated cell lines:
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Shimizu T, Matsuo-Takasaki M, Luijkx D, Takami M, Arai Y, Noguchi M, Nakamura Y, Hayata T, Saito MK, Hayashi Y
Generation of human induced pluripotent stem cell lines derived from four DiGeorge syndrome patients with 22q11.2 deletion
Shimizu T et al. Generation of human induced pluripotent stem cell lines derived from four DiGeorge syndrome patients with 22q11.2 deletion. . 2022-05-00. Pubmed ID: 35292424; DOI: 10.1016/j.scr.2022.102744 BRCi017-ABRCi018-ABRCi019-ABRCi020-A 2022-05-00 2022-05-00 PubMed: 35292424 DOI: 10.1016/j.scr.2022.102744 -
Liu Y, Jin Y, Chen T, Wu Y, Peng X, Li W, Wei S, Chen M, Zou Q, Guo S, Xu J, Tang C, Zhou X
Generation of a homozygous ARHGAP11B knockout hiPSC line by CRISPR/Cas9 system
Liu Y et al. Generation of a homozygous ARHGAP11B knockout hiPSC line by CRISPR/Cas9 system. . 2022-05-00. Pubmed ID: 35358830; DOI: 10.1016/j.scr.2022.102764 WYUi001-A 2022-05-00 2022-05-00 PubMed: 35358830 DOI: 10.1016/j.scr.2022.102764Associated cell lines:
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Hommersom MP, Bijnagte-Schoenmaker C, Albert S, van de Warrenburg BPC, Nadif Kasri N, van Bokhoven H
Generation of induced pluripotent stem cell lines carrying monoallelic (UCSFi001-A-60) or biallelic (UCSFi001-A-61; UCSFi001-A-62) frameshift variants in CACNA1A using CRISPR/Cas9
Hommersom MP et al. Generation of induced pluripotent stem cell lines carrying monoallelic (UCSFi001-A-60) or biallelic (UCSFi001-A-61; UCSFi001-A-62) frameshift variants in CACNA1A using CRISPR/Cas9. . 2022-05-00. Pubmed ID: 35286975; DOI: 10.1016/j.scr.2022.102730 UCSFi001-AUCSFi001-A-60UCSFi001-A-61UCSFi001-A-62 2022-05-00 2022-05-00 PubMed: 35286975 DOI: 10.1016/j.scr.2022.102730Associated cell lines:
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Chen Z, Lv H, Yu J, Fang S, Li F
Generation of an induced pluripotent stem cell line SJTUXHi001-A from an autism spectrum disorder patient carrying a heterozygous mutation in HDAC8 (p.P359S)
Chen Z et al. Generation of an induced pluripotent stem cell line SJTUXHi001-A from an autism spectrum disorder patient carrying a heterozygous mutation in HDAC8 (p.P359S). . 2022-05-00. Pubmed ID: 35358829; DOI: 10.1016/j.scr.2022.102756 SJTUXHi001-A 2022-05-00 2022-05-00 PubMed: 35358829 DOI: 10.1016/j.scr.2022.102756Associated cell lines:
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Lin A, Kang X, Xu Y, Feng X, Zhang S, Zhao H, Wu D, Han X
Human induced pluripotent stem cells derived from a patient with a mutation of FBN1c.1858C > T (p. Pro620Ser)
Lin A et al. Human induced pluripotent stem cells derived from a patient with a mutation of FBN1c.1858C > T (p. Pro620Ser). . 2022-05-00. Pubmed ID: 35339882; DOI: 10.1016/j.scr.2022.102759 FUHSi001-A 2022-05-00 2022-05-00 PubMed: 35339882 DOI: 10.1016/j.scr.2022.102759Associated cell lines:
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Sabitha KR, Chandran D, Shetty AK, Upadhya D
Delineating the Neuropathology of Lysosomal Storage Diseases Using Patient-Derived Induced Pluripotent Stem Cells
Sabitha KR et al. Delineating the Neuropathology of Lysosomal Storage Diseases Using Patient-Derived Induced Pluripotent Stem Cells. . 2022-05-00. Pubmed ID: 35316126; DOI: 10.1089/scd.2021.0304 TRNDi004-ITRNDi009-CPUMCi001-A 2022-05-00 2022-05-00 PubMed: 35316126 DOI: 10.1089/scd.2021.0304Associated cell lines:
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Hu X, Xiong S, Zhou X, Sun L
Generation of a human induced pluripotent stem cell line FMUPDCi001-A from a patient with mental retardation, autosomal recessive 36 (MRT36) carrying the variants c.219dupA and c.587C > T in ADAT3
Hu X et al. Generation of a human induced pluripotent stem cell line FMUPDCi001-A from a patient with mental retardation, autosomal recessive 36 (MRT36) carrying the variants c.219dupA and c.587C > T in ADAT3. . 2022-05-00. Pubmed ID: 35405382; DOI: 10.1016/j.scr.2022.102777 FMUPDCi001-A 2022-05-00 2022-05-00 PubMed: 35405382 DOI: 10.1016/j.scr.2022.102777Associated cell lines:
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Guo R, Liu X, Zhang J, Ma X, Gou D, Ma Z, Wang L, Ma J, Cui H
Integration-free induced pluripotent stem cell line derived from a 62-years-old male donor with APOE-epsilon4/epsilon4 alleles
Guo R et al. Integration-free induced pluripotent stem cell line derived from a 62-years-old male donor with APOE-epsilon4/epsilon4 alleles. . 2022-05-00. Pubmed ID: 35305470; DOI: 10.1016/j.scr.2022.102746 HEBHMUi001-AHEBHMUi011-A 2022-05-00 2022-05-00 PubMed: 35305470 DOI: 10.1016/j.scr.2022.102746Associated cell lines:
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Li R, Zhao Y, Yourick JJ, Sprando RL, Gao X
Phenotypical, functional and transcriptomic comparison of two modified methods of hepatocyte differentiation from human induced pluripotent stem cells
Li R et al. Phenotypical, functional and transcriptomic comparison of two modified methods of hepatocyte differentiation from human induced pluripotent stem cells. . 2022-05-00. Pubmed ID: 35371477; DOI: 10.3892/br.2022.1526; PMC: PMC8972237 OARSAi002-A 2022-05-00 2022-05-00 PubMed: 35371477 DOI: 10.3892/br.2022.1526Associated cell lines:
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Sun J, Zeng R, Liu Y, Xi S, Sun T, Qian J, Yi Z, Qin S
Generation of ultra-treatment-resistant schizophrenia patient-derived induced pluripotent stem cell line UJSi002-A
Sun J et al. Generation of ultra-treatment-resistant schizophrenia patient-derived induced pluripotent stem cell line UJSi002-A. . 2022-05-00. Pubmed ID: 35367693; DOI: 10.1016/j.scr.2022.102766 UJSi001-AUJSi002-A 2022-05-00 2022-05-00 PubMed: 35367693 DOI: 10.1016/j.scr.2022.102766 -
Bchetnia M, Martineau L, Racine V, Powell J, McCuaig C, Morin C, Dupérée A, Gros-Louis F, Laprise C
Generation of two induced pluripotent stem cell lines (UQACi002-A and UQACi005-A) from two patients with KRT14 epidermolysis bullosa simplex mutations
Bchetnia M et al. Generation of two induced pluripotent stem cell lines (UQACi002-A and UQACi005-A) from two patients with KRT14 epidermolysis bullosa simplex mutations. . 2022-05-00. Pubmed ID: 35334406; DOI: 10.1016/j.scr.2022.102750 UQACi002-AUQACi005-A 2022-05-00 2022-05-00 PubMed: 35334406 DOI: 10.1016/j.scr.2022.102750Associated cell lines:
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Gridina MM, Nurislamov AR, Minina JM, Lopatkina ME, Drozdov GV, Vasilyev SA, Minaycheva LI, Belyaeva EO, Nikitina TV, Kashevarova AA, Lebedev IN, Karamysheva TV, Rubtsov NB, Serov OL
Generation of iPS cell line (ICGi040-A) from skin fibroblasts of a patient with ring small supernumerary marker chromosome 4
Gridina MM et al. Generation of iPS cell line (ICGi040-A) from skin fibroblasts of a patient with ring small supernumerary marker chromosome 4. . 2022-05-00. Pubmed ID: 35303600; DOI: 10.1016/j.scr.2022.102740 ICGi032-AICGi040-A 2022-05-00 2022-05-00 PubMed: 35303600 DOI: 10.1016/j.scr.2022.102740 -
Metzl-Raz E, Bharucha N, Arthur Ataam J, Gavidia AA, Greenleaf WJ, Karakikes I
Generation of a dual edited human induced pluripotent stem cell Myl7-GFP reporter line with inducible CRISPRi/dCas9
Metzl-Raz E et al. Generation of a dual edited human induced pluripotent stem cell Myl7-GFP reporter line with inducible CRISPRi/dCas9. . 2022-05-00. Pubmed ID: 35325819; DOI: 10.1016/j.scr.2022.102754; PMC: PMC9169598 SCVIi038-A 2022-05-00 2022-05-00 PubMed: 35325819 DOI: 10.1016/j.scr.2022.102754Associated cell lines:
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Schindeler A, Lee LR, O'Donohue AK, Ginn SL, Munns CF
Curative Cell and Gene Therapy for Osteogenesis Imperfecta
Schindeler A et al. Curative Cell and Gene Therapy for Osteogenesis Imperfecta. . 2022-05-00. Pubmed ID: 35306687; DOI: 10.1002/jbmr.4549; PMC: PMC9324990 MCRIi001-AMCRIi001-A-1 2022-05-00 2022-05-00 PubMed: 35306687 DOI: 10.1002/jbmr.4549Associated cell lines:
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Lee HM, Kim AH, Hwang S, Jung J, Seol H, Sung JJ, Jeong SM, Choi YM, Jun JK, Kim HS, Jang J
Generation of αMHC-EGFP knock-in in human pluripotent stem cell line, SNUe003-A-3 using CRISPR/Cas9-based gene targeting
Lee HM et al. Generation of αMHC-EGFP knock-in in human pluripotent stem cell line, SNUe003-A-3 using CRISPR/Cas9-based gene targeting. . 2022-05-00. Pubmed ID: 35427904; DOI: 10.1016/j.scr.2022.102779 SNUe003-ASNUe003-A-2SNUe003-A-3 2022-05-00 2022-05-00 PubMed: 35427904 DOI: 10.1016/j.scr.2022.102779Associated cell lines:
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Maranga C, Pereira C, Raposo AC, Vieira A, Duarte S, Bekman EP, Milagre I, da Rocha ST
Generation and characterization of induced pluripotent stem cell line (IBBISTi004-A) from an Angelman syndrome patient carrying a class II deletion of the maternal chromosome 15q11.2-q13
Maranga C et al. Generation and characterization of induced pluripotent stem cell line (IBBISTi004-A) from an Angelman syndrome patient carrying a class II deletion of the maternal chromosome 15q11.2-q13. . 2022-05-00. Pubmed ID: 35339881; DOI: 10.1016/j.scr.2022.102757 IBBISTi004-AIBBISTi004-BIBBISTi004-C 2022-05-00 2022-05-00 PubMed: 35339881 DOI: 10.1016/j.scr.2022.102757Associated cell lines:
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Manhas A, Jahng JWS, Vera CD, Shenoy SP, Knowles JW, Wu JC
Generation of two iPSC lines from hypertrophic cardiomyopathy patients carrying MYBPC3 and PRKAG2 variants
Manhas A et al. Generation of two iPSC lines from hypertrophic cardiomyopathy patients carrying MYBPC3 and PRKAG2 variants. . 2022-05-00. Pubmed ID: 35413566; DOI: 10.1016/j.scr.2022.102774; PMC: PMC9708393 SCVIi036-ASCVIi037-A 2022-05-00 2022-05-00 PubMed: 35413566 DOI: 10.1016/j.scr.2022.102774Associated cell lines:
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Cuadros Gamboa AL, Benfante R, Nizzardo M, Bachetti T, Pelucchi P, Melzi V, Arzilli C, Peruzzi M, Reinbold RA, Cardani S, Morrone A, Guerrini R, Zucchi I, Corti S, Ceccherini I, Piumelli R, Nassi N, Di Lascio S, Fornasari D
Generation of two hiPSC lines (UMILi027-A and UMILi028-A) from early and late-onset Congenital Central hypoventilation Syndrome (CCHS) patients carrying a polyalanine expansion mutation in the PHOX2B gene
Cuadros Gamboa AL et al. Generation of two hiPSC lines (UMILi027-A and UMILi028-A) from early and late-onset Congenital Central hypoventilation Syndrome (CCHS) patients carrying a polyalanine expansion mutation in the PHOX2B gene. . 2022-05-00. Pubmed ID: 35421844; DOI: 10.1016/j.scr.2022.102781 UMILi027-AUMILi028-A 2022-05-00 2022-05-00 PubMed: 35421844 DOI: 10.1016/j.scr.2022.102781Associated cell lines:
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Iuso A, Zhang F, Rusha E, Campbell B, Dorn T, Zanuttigh E, Haas D, Anikster Y, Lederer G, Pertek A, Nteli P, Laugwitz KL, Moretti A
Generation of two human iPSC lines, HMGUi003-A and MRIi028-A, carrying pathogenic biallelic variants in the PPCS gene
Iuso A et al. Generation of two human iPSC lines, HMGUi003-A and MRIi028-A, carrying pathogenic biallelic variants in the PPCS gene. . 2022-05-00. Pubmed ID: 35397396; DOI: 10.1016/j.scr.2022.102773 MRIi028-AHMGUi003-A 2022-05-00 2022-05-00 PubMed: 35397396 DOI: 10.1016/j.scr.2022.102773Associated cell lines:
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Harper RL, Ferrante EA, Boehm M
Development of vascular disease models to explore disease causation and pathomechanisms of rare vascular diseases
Harper RL et al. Development of vascular disease models to explore disease causation and pathomechanisms of rare vascular diseases. . 2022-05-00. Pubmed ID: 35233690; DOI: 10.1007/s00281-022-00925-9; PMC: PMC8887661 NIHTVBi004-ANIHTVBi005-ANIHTVBi006-ANIHTVBi007-ANIHTVBi008-ANIHTVBi011-ANIHTVBi012-ANIHTVBi013-ANIHTVBi014-A 2022-05-00 2022-05-00 PubMed: 35233690 DOI: 10.1007/s00281-022-00925-9Associated cell lines:
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Tang PC, V Roche M, Young Um S, Gosstola NC, Young Kim M, Yoon Choi B, Dykxhoorn DM, Zhong Liu X
Characterization of an induced pluripotent stem cell line (UMi040-A) bearing an auditory neuropathy spectrum disorder-associated variant in TMEM43
Tang PC et al. Characterization of an induced pluripotent stem cell line (UMi040-A) bearing an auditory neuropathy spectrum disorder-associated variant in TMEM43. . 2022-05-00. Pubmed ID: 35364395; DOI: 10.1016/j.scr.2022.102758; PMC: PMC9089836 UMi040-A 2022-05-00 2022-05-00 PubMed: 35364395 DOI: 10.1016/j.scr.2022.102758Associated cell lines:
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Breyer M, Klein T, Klug K, Klopocki E, Üçeyler N
Generation of the induced pluripotent stem cell line UKWNLi005-A derived from a patient with the GLA mutation c.376A > G of unknown pathogenicity in Fabry disease
Breyer M et al. Generation of the induced pluripotent stem cell line UKWNLi005-A derived from a patient with the GLA mutation c.376A > G of unknown pathogenicity in Fabry disease. . 2022-05-00. Pubmed ID: 35325818; DOI: 10.1016/j.scr.2022.102747 UKWNLi005-A 2022-05-00 2022-05-00 PubMed: 35325818 DOI: 10.1016/j.scr.2022.102747Associated cell lines:
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Chen D, Wang T, Ye X, Xu X, Xia W, Fu Y
Generation of induced pluripotent stem cell line derived from FNAIT patient with CD36 deficiency mutations
Chen D et al. Generation of induced pluripotent stem cell line derived from FNAIT patient with CD36 deficiency mutations. . 2022-05-00. Pubmed ID: 35305469; DOI: 10.1016/j.scr.2022.102749 SYSUSCi002-A 2022-05-00 2022-05-00 PubMed: 35305469 DOI: 10.1016/j.scr.2022.102749Associated cell lines:
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Zhu W, Zhou Y, Wang Q, Li J, Chu S, Jin W, Mao C, Dong L, Gao J, Xu Q
Generation of a human induced pluripotent stem cell (iPSC) line from skin fibroblasts of a patient carrying an E363Q mutation in PSEN1 gene
Zhu W et al. Generation of a human induced pluripotent stem cell (iPSC) line from skin fibroblasts of a patient carrying an E363Q mutation in PSEN1 gene. . 2022-05-00. Pubmed ID: 35421846; DOI: 10.1016/j.scr.2022.102769 PUMCi003-A 2022-05-00 2022-05-00 PubMed: 35421846 DOI: 10.1016/j.scr.2022.102769Associated cell lines:
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Novak G, Finkbeiner S, Skibinski G, Bernini M, Donato C, Skupin A
Generation of two human induced pluripotent stem cell lines from fibroblasts of Parkinson's disease patients carrying the ILE368ASN mutation in PINK1 (LCSBi002) and the R275W mutation in Parkin (LCSBI004)
Novak G et al. Generation of two human induced pluripotent stem cell lines from fibroblasts of Parkinson's disease patients carrying the ILE368ASN mutation in PINK1 (LCSBi002) and the R275W mutation in Parkin (LCSBI004). . 2022-05-00. Pubmed ID: 35378365; DOI: 10.1016/j.scr.2022.102765 LCSBi002-BLCSBi002-CLCSBi004-ALCSBi004-B 2022-05-00 2022-05-00 PubMed: 35378365 DOI: 10.1016/j.scr.2022.102765Associated cell lines:
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Sowmithra S, Jain NK, Bhonde R, Datta I
Recovery of Human Embryonic Stem Cells-Derived Neural Progenitors Exposed to Hypoxic-Ischemic-Reperfusion Injury by Indirect Exposure to Wharton's Jelly Mesenchymal Stem Cells Through Phosphatidyl-inositol-3-Kinase Pathway
Sowmithra S et al. Recovery of Human Embryonic Stem Cells-Derived Neural Progenitors Exposed to Hypoxic-Ischemic-Reperfusion Injury by Indirect Exposure to Wharton's Jelly Mesenchymal Stem Cells Through Phosphatidyl-inositol-3-Kinase Pathway. . 2022-05-00. Pubmed ID: 33206286; DOI: 10.1007/s10571-020-01007-w NIMHi001-A 2022-05-00 2022-05-00 PubMed: 33206286 DOI: 10.1007/s10571-020-01007-wAssociated cell lines:
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Zhu J, Chen Y, Cao X, Li Q, Shao L, Teng X, Yu Y, Shen Z
Generation of a Human iPSC (ICSSUi002-A) with MTHFR SNP (rs1801133, TT) from Thoracic Aortic Dissection Patient
Zhu J et al. Generation of a Human iPSC (ICSSUi002-A) with MTHFR SNP (rs1801133, TT) from Thoracic Aortic Dissection Patient. . 2022-05-00. Pubmed ID: 35305471; DOI: 10.1016/j.scr.2022.102753 ICSSUi002-A 2022-05-00 2022-05-00 PubMed: 35305471 DOI: 10.1016/j.scr.2022.102753Associated cell lines:
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Xue N, Wang Y, Xu X, Jiang X, Li C, Wang J, Zhou P, Cao Y, Wei Z
Establishment of pluripotent stem cell line induced by PATL2 heterozygous mutation in patients with oocyte maturation defect-4
Xue N et al. Establishment of pluripotent stem cell line induced by PATL2 heterozygous mutation in patients with oocyte maturation defect-4. . 2022-05-00. Pubmed ID: 35397397; DOI: 10.1016/j.scr.2022.102776 AMUFAHi003-A 2022-05-00 2022-05-00 PubMed: 35397397 DOI: 10.1016/j.scr.2022.102776Associated cell lines:
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Shi M, Shang S, Yang Y, Li Q, Bai XY
Establishment of PLAFMCi007-A, an induced pluripotent stem cell line, from peripheral blood mononuclear cells (PBMCs) of a healthy adult woman
Shi M et al. Establishment of PLAFMCi007-A, an induced pluripotent stem cell line, from peripheral blood mononuclear cells (PBMCs) of a healthy adult woman. . 2022-05-00. Pubmed ID: 35339884; DOI: 10.1016/j.scr.2022.102760 CPGHi007-A 2022-05-00 2022-05-00 PubMed: 35339884 DOI: 10.1016/j.scr.2022.102760Associated cell lines:
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Tisch M, Carmen De Mingo Alemany M, Suarez-Cubero M, Fauth C, Defrancesco M, Zschocke J, Günther K, Edenhofer F
Generation of the human induced pluripotent stem cell line (IBKMOLi002-A) from PBMCs of a patient carrying the heterozygous L271H mutation of the voltage-gated calcium channel subunit Ca(v)1.3-encoding CACNA1D gene
Tisch M et al. Generation of the human induced pluripotent stem cell line (IBKMOLi002-A) from PBMCs of a patient carrying the heterozygous L271H mutation of the voltage-gated calcium channel subunit Ca(v)1.3-encoding CACNA1D gene. . 2022-05-00. Pubmed ID: 35453044; DOI: 10.1016/j.scr.2022.102784 IBKMOLi002-A 2022-05-00 2022-05-00 PubMed: 35453044 DOI: 10.1016/j.scr.2022.102784Associated cell lines:
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Banal C, Lefort N
Generation and characterization of IMAGINi013-A, an induced pluripotent stem cell line generated from a healthy donor
Banal C et al. Generation and characterization of IMAGINi013-A, an induced pluripotent stem cell line generated from a healthy donor. . 2022-05-00. Pubmed ID: 35334405; DOI: 10.1016/j.scr.2022.102755 IMAGINi004-AIMAGINi005-AIMAGINi011-AIMAGINi013-A 2022-05-00 2022-05-00 PubMed: 35334405 DOI: 10.1016/j.scr.2022.102755Associated cell lines:
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Nehra S, Sharma V, Singh M, Singhal P, Singhal N
Generation of integration free hiPSCs clones, NSi001-A, NSi001-B, and NSi001-C from peripheral blood mononuclear cells of an individual with down syndrome having Robertsonian translocation
Nehra S et al. Generation of integration free hiPSCs clones, NSi001-A, NSi001-B, and NSi001-C from peripheral blood mononuclear cells of an individual with down syndrome having Robertsonian translocation. . 2022-05-00. Pubmed ID: 35381521; DOI: 10.1016/j.scr.2022.102771 NSi001-ANSi001-BNSi001-C 2022-05-00 2022-05-00 PubMed: 35381521 DOI: 10.1016/j.scr.2022.102771 -
Ura H, Togi S, Iwata Y, Ozaki M, Niida Y
Establishment of a human induced pluripotent stem cell line, KMUGMCi001-A, from a patient bearing a heterozygous c.772 + 3_772 + 4dup mutation in the ACVRL1 gene leading Telangiectasia, hereditary hemorrhagic, type 2 (HHT2)
Ura H et al. Establishment of a human induced pluripotent stem cell line, KMUGMCi001-A, from a patient bearing a heterozygous c.772 + 3_772 + 4dup mutation in the ACVRL1 gene leading Telangiectasia, hereditary hemorrhagic, type 2 (HHT2). . 2022-05-00. Pubmed ID: 35279593; DOI: 10.1016/j.scr.2022.102743 KMUGMCi001-A 2022-05-00 2022-05-00 PubMed: 35279593 DOI: 10.1016/j.scr.2022.102743Associated cell lines:
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Zhang F, Meier AB, Sinnecker D, Engelhardt S, Lipp P, Laugwitz KL, Dorn T, Moretti A
Generation of heterozygous (MRli003-A-5) and homozygous (MRli003-A-6) voltage-sensing knock-in human iPSC lines by CRISPR/Cas9 editing of the AAVS1 locus
Zhang F et al. Generation of heterozygous (MRli003-A-5) and homozygous (MRli003-A-6) voltage-sensing knock-in human iPSC lines by CRISPR/Cas9 editing of the AAVS1 locus. . 2022-05-00. Pubmed ID: 35421847; DOI: 10.1016/j.scr.2022.102785 MRIi003-AMRIi003-A-5MRIi003-A-6 2022-05-00 2022-05-00 PubMed: 35421847 DOI: 10.1016/j.scr.2022.102785Associated cell lines:
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Hong JH, Kim JH, Kang KW, Lee BH, Park Y, Kim BS
Generation of a human induced pluripotent stem cell line KUMi006 from a patient with multiple myeloma
Hong JH et al. Generation of a human induced pluripotent stem cell line KUMi006 from a patient with multiple myeloma. . 2022-05-00. Pubmed ID: 35397398; DOI: 10.1016/j.scr.2022.102767 KUMi006-A 2022-05-00 2022-05-00 PubMed: 35397398 DOI: 10.1016/j.scr.2022.102767Associated cell lines:
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Lee MP, Waldhaus J
In vitro and in vivo models: What have we learnt about inner ear regeneration and treatment for hearing loss?
Lee MP et al. In vitro and in vivo models: What have we learnt about inner ear regeneration and treatment for hearing loss?. . 2022-05-00. Pubmed ID: 35577314; DOI: 10.1016/j.mcn.2022.103736; PMC: PMC9551661 TYWHSTi002-A 2022-05-00 2022-05-00 PubMed: 35577314 DOI: 10.1016/j.mcn.2022.103736Associated cell lines:
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Liu Y, Liu Y, Jia Y, Lv J, Sun D, Yin Y, Liu N, Su B, Sun G
Generation of an induced pluripotent stem cell (iPSC) line from a diabetic patient with glucagon receptor (GCGR) p.W83X mutation
Liu Y et al. Generation of an induced pluripotent stem cell (iPSC) line from a diabetic patient with glucagon receptor (GCGR) p.W83X mutation. . 2022-05-00. Pubmed ID: 35381520; DOI: 10.1016/j.scr.2022.102745 SJHi001-ASJHi002-A 2022-05-00 2022-05-00 PubMed: 35381520 DOI: 10.1016/j.scr.2022.102745 -
Lorenz C, Zink A, Henke MT, Staege S, Mlody B, Bünning M, Wanker E, Diecke S, Schuelke M, Prigione A
Generation of four iPSC lines from four patients with Leigh syndrome carrying homoplasmic mutations m.8993T > G or m.8993T > C in the mitochondrial gene MT-ATP6
Lorenz C et al. Generation of four iPSC lines from four patients with Leigh syndrome carrying homoplasmic mutations m.8993T > G or m.8993T > C in the mitochondrial gene MT-ATP6. . 2022-05-00. Pubmed ID: 35279592; DOI: 10.1016/j.scr.2022.102742 MDCi007-AMDCi008-AMDCi009-AMDCi010-A 2022-05-00 2022-05-00 PubMed: 35279592 DOI: 10.1016/j.scr.2022.102742 -
Yu X, Wang H, Xiao F, Jiang S, Li K, Chen Q, Wang G, Kong F, Zhao S
Generation of the integration-free induced pluripotent stem cell line (FHUSTCi001-A) from a patient with glomerulopathy with fibronectin deposits harboring FN1 mutation
Yu X et al. Generation of the integration-free induced pluripotent stem cell line (FHUSTCi001-A) from a patient with glomerulopathy with fibronectin deposits harboring FN1 mutation. . 2022-05-00. Pubmed ID: 35395622; DOI: 10.1016/j.scr.2022.102751 FJMUi001-AFHUSTCi001-A 2022-05-00 2022-05-00 PubMed: 35395622 DOI: 10.1016/j.scr.2022.102751Associated cell lines:
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Sun M, Li J, Shang S, Bai X, Cai G, Li Q
Generation of induced pluripotent stem cells from peripheral blood mononuclear cells obtained from an adult with autosomal recessive polycystic kidney disease
Sun M et al. Generation of induced pluripotent stem cells from peripheral blood mononuclear cells obtained from an adult with autosomal recessive polycystic kidney disease. . 2022-05-00. Pubmed ID: 35405383; DOI: 10.1016/j.scr.2022.102772 CPGHi008-A 2022-05-00 2022-05-00 PubMed: 35405383 DOI: 10.1016/j.scr.2022.102772Associated cell lines:
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Iannello G, Patel A, Sirabella D, Corneo B, Thaker V
Corrigendum to "Generation of the iPSC line CUIMCi003-A derived from a patient with severe early onset obesity" [Stem Cell Res 54 (2021) 102432]
Iannello G et al. Corrigendum to "Generation of the iPSC line CUIMCi003-A derived from a patient with severe early onset obesity" [Stem Cell Res 54 (2021) 102432]. . 2022-05-00. Pubmed ID: 35390757; DOI: 10.1016/j.scr.2022.102778; PMC: PMC10002150 CUIMCi003-A 2022-05-00 2022-05-00 PubMed: 35390757 DOI: 10.1016/j.scr.2022.102778Associated cell lines:
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Wang Y, Liu Z, Chen C, Li Y, Guan M, Xu B, Guo Y
Verification of an iPSC line (LZUi002-A) from a patient with a novel mutation in the TBL1X gene
Wang Y et al. Verification of an iPSC line (LZUi002-A) from a patient with a novel mutation in the TBL1X gene. . 2022-05-00. Pubmed ID: 35339883; DOI: 10.1016/j.scr.2022.102761 LZUi002-A 2022-05-00 2022-05-00 PubMed: 35339883 DOI: 10.1016/j.scr.2022.102761Associated cell lines:
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Rozanska A, Cerna-Chavez R, Queen R, Collin J, Zerti D, Dorgau B, Beh CS, Davey T, Coxhead J, Hussain R, Al-Aama J, Steel DH, Benvenisty N, Armstrong L, Parulekar M, Lako M
pRB-Depleted Pluripotent Stem Cell Retinal Organoids Recapitulate Cell State Transitions of Retinoblastoma Development and Suggest an Important Role for pRB in Retinal Cell Differentiation
Rozanska A et al. pRB-Depleted Pluripotent Stem Cell Retinal Organoids Recapitulate Cell State Transitions of Retinoblastoma Development and Suggest an Important Role for pRB in Retinal Cell Differentiation. . 2022-04-29. Pubmed ID: 35325233; DOI: 10.1093/stcltm/szac008; PMC: PMC9052432 VRFi001-A 2022-04-29 2022-04-29 PubMed: 35325233 DOI: 10.1093/stcltm/szac008Associated cell lines:
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Rahman MA, Rahman MDH, Mamun-Or-Rashid ANM, Hwang H, Chung S, Kim B, Rhim H
Autophagy Modulation in Aggresome Formation: Emerging Implications and Treatments of Alzheimer's Disease
Rahman MA et al. Autophagy Modulation in Aggresome Formation: Emerging Implications and Treatments of Alzheimer's Disease. . 2022-04-29. Pubmed ID: 35625764; DOI: 10.3390/biomedicines10051027; PMC: PMC9138936 ZZUi010-AICCSICi006-A 2022-04-29 2022-04-29 PubMed: 35625764 DOI: 10.3390/biomedicines10051027Associated cell lines:
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Solomon Shiden, Sampathkumar Nirmal Kumar, Carre Ivo, Mondal Mrityunjoy, Chennell George, Vernon Anthony C., Ruepp Marc-David, Mitchell Jacqueline
Heterozygous expression of the Alzheimer’s disease protective PLCγ2 P522R variant enhances Aβ clearance while preserving synapses.
Solomon Shiden et al. Heterozygous expression of the Alzheimer’s disease protective PLCγ2 P522R variant enhances Aβ clearance while preserving synapses. . 2022-04-20. DOI: 10.21203/rs.3.rs-1420006/v2 BIONi010-C 2022-04-20 2022-04-20 DOI: 10.21203/rs.3.rs-1420006/v2Associated cell lines:
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Vanhoye X, Janin A, Caillaud A, Rimbert A, Venet F, Gossez M, Dijk W, Marmontel O, Nony S, Chatelain C, Durand C, Lindenbaum P, Rieusset J, Cariou B, Moulin P, Di Filippo M
APOB CRISPR-Cas9 Engineering in Hypobetalipoproteinemia: A Promising Tool for Functional Studies of Novel Variants
Vanhoye X et al. APOB CRISPR-Cas9 Engineering in Hypobetalipoproteinemia: A Promising Tool for Functional Studies of Novel Variants. . 2022-04-13. Pubmed ID: 35457099; DOI: 10.3390/ijms23084281; PMC: PMC9030618 CIBi009-A 2022-04-13 2022-04-13 PubMed: 35457099 DOI: 10.3390/ijms23084281Associated cell lines:
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Nayak Ritu, Rosh Idan, Rabinski Tatiana, Percia Menachem Mendel, Stern Shani
Generation and characterization of iPSC lines (UOHi001-A, UOHi002-A) From a patient with SHANK3 mutation and her healthy mother
Nayak Ritu et al. Generation and characterization of iPSC lines (UOHi001-A, UOHi002-A) From a patient with SHANK3 mutation and her healthy mother. . 2022-04-13. DOI: 10.1101/2022.04.13.486968 UOHi002-AUOHi003-A 2022-04-13 2022-04-13 DOI: 10.1101/2022.04.13.486968 -
Rossbach B, Hariharan K, Mah N, Oh SJ, Volk HD, Reinke P, Kurtz A
Human iPSC-Derived Renal Cells Change Their Immunogenic Properties during Maturation: Implications for Regenerative Therapies
Rossbach B et al. Human iPSC-Derived Renal Cells Change Their Immunogenic Properties during Maturation: Implications for Regenerative Therapies. . 2022-04-13. Pubmed ID: 35456007; DOI: 10.3390/cells11081328; PMC: PMC9032821 BCRTi004-ABCRTi005-A 2022-04-13 2022-04-13 PubMed: 35456007 DOI: 10.3390/cells11081328Associated cell lines:
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Rai D, Iwanami M, Takahashi Y, Komuta Y, Aoi N, Umezawa A, Seko Y
Evaluation of photoreceptor-directed fibroblasts derived from retinitis pigmentosa patients with defects in the EYS gene: a possible cost-effective cellular model for mechanism-oriented drug
Rai D et al. Evaluation of photoreceptor-directed fibroblasts derived from retinitis pigmentosa patients with defects in the EYS gene: a possible cost-effective cellular model for mechanism-oriented drug. . 2022-04-11. Pubmed ID: 35410372; DOI: 10.1186/s13287-022-02827-x; PMC: PMC8996485 FRIMOi001-A 2022-04-11 2022-04-11 PubMed: 35410372 DOI: 10.1186/s13287-022-02827-xAssociated cell lines:
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Vojnits K, Nakanishi M, Porras D, Kim Y, Feng Z, Golubeva D, Bhatia M
Developing CRISPR/Cas9-Mediated Fluorescent Reporter Human Pluripotent Stem-Cell Lines for High-Content Screening
Vojnits K et al. Developing CRISPR/Cas9-Mediated Fluorescent Reporter Human Pluripotent Stem-Cell Lines for High-Content Screening. . 2022-04-09. Pubmed ID: 35458632; DOI: 10.3390/molecules27082434; PMC: PMC9025795 WAe009-A 2022-04-09 2022-04-09 PubMed: 35458632 DOI: 10.3390/molecules27082434Associated cell lines:
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Brodehl A, Gerull B
Genetic Insights into Primary Restrictive Cardiomyopathy
Brodehl A et al. Genetic Insights into Primary Restrictive Cardiomyopathy. . 2022-04-08. Pubmed ID: 35456187; DOI: 10.3390/jcm11082094; PMC: PMC9027761 FAMRCi009-AFAMRCi010-A 2022-04-08 2022-04-08 PubMed: 35456187 DOI: 10.3390/jcm11082094Associated cell lines:
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Sequiera GL, Srivastava A, Sareen N, Yan W, Alagarsamy KN, Verma E, Aghanoori MR, Aliani M, Kumar A, Fernyhough P, Rockman-Greenberg C, Dhingra S
Development of iPSC-based clinical trial selection platform for patients with ultrarare diseases
Sequiera GL et al. Development of iPSC-based clinical trial selection platform for patients with ultrarare diseases. . 2022-04-08. Pubmed ID: 35394834; DOI: 10.1126/sciadv.abl4370; PMC: PMC8993122 UOMi001-AUOMi002-A 2022-04-08 2022-04-08 PubMed: 35394834 DOI: 10.1126/sciadv.abl4370 -
Gather F, Ihrig-Biedert I, Kohlhas P, Krutenko T, Peitz M, Brüstle O, Pautz A, Kleinert H
A specific, non-immune system-related isoform of the human inducible nitric oxide synthase is expressed during differentiation of human stem cells into various cell types
Gather F et al. A specific, non-immune system-related isoform of the human inducible nitric oxide synthase is expressed during differentiation of human stem cells into various cell types. . 2022-04-07. Pubmed ID: 35392923; DOI: 10.1186/s12964-022-00855-x; PMC: PMC8991583 UKBi011-AUKBi013-AUKBi015-AUKBi015-B 2022-04-07 2022-04-07 PubMed: 35392923 DOI: 10.1186/s12964-022-00855-x -
Calvillo Laura, Redaelli Veronica, Ludwig Nicola, Qaswal Abdallah Barjas, Ghidoni Alice, Faini Andrea, Rosa Debora, Lombardi Carolina, Pengo Martino, Bossolasco Patrizia, Silani Vincenzo, Parati Gianfranco
Quantum Biology Research Meets Pathophysiology and Therapeutic Mechanisms: A Biomedical Perspective
Calvillo Laura et al. Quantum Biology Research Meets Pathophysiology and Therapeutic Mechanisms: A Biomedical Perspective. . 2022-04-04. DOI: 10.3390/quantum4020011 PSMi006-A 2022-04-04 2022-04-04 DOI: 10.3390/quantum4020011Associated cell lines:
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Lee SE, Choi H, Shin N, Kong D, Kim NG, Kim HY, Kim MJ, Choi SW, Kim YB, Kang KS
Zika virus infection accelerates Alzheimer's disease phenotypes in brain organoids
Lee SE et al. Zika virus infection accelerates Alzheimer's disease phenotypes in brain organoids. . 2022-04-02. Pubmed ID: 35368019; DOI: 10.1038/s41420-022-00958-x; PMC: PMC8976422 KSCBi005-A 2022-04-02 2022-04-02 PubMed: 35368019 DOI: 10.1038/s41420-022-00958-xAssociated cell lines:
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Zhang L, Liu D, Li B, Xie J, Liu J, Zhang Z
Single nucleotide polymorphism genotyping of ALDH2 gene based on asymmetric PCR and fluorescent probe-mediated melting curves
Zhang L et al. Single nucleotide polymorphism genotyping of ALDH2 gene based on asymmetric PCR and fluorescent probe-mediated melting curves. . 2022-04-01. Pubmed ID: 34864041; DOI: 10.1016/j.ab.2021.114509 FIRDIi001-A 2022-04-01 2022-04-01 PubMed: 34864041 DOI: 10.1016/j.ab.2021.114509Associated cell lines:
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Gill PK, Hegele RA
Familial combined hyperlipidemia is a polygenic trait
Gill PK et al. Familial combined hyperlipidemia is a polygenic trait. . 2022-04-01. Pubmed ID: 34690300; DOI: 10.1097/mol.0000000000000796 SDQLCHi042-A 2022-04-01 2022-04-01 PubMed: 34690300 DOI: 10.1097/mol.0000000000000796Associated cell lines:
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Sun W, Yi D, Zhu L, Zeng J, Liu Y, Chang J, Teng J, Zhang Y, Dong Y, Pan X, Chen Y, Zhou Y, Lai M, Zhou Q, Liu J, Chen B, Ma F
RUNX1 overexpression triggers TGF-β signaling to upregulate p15 and thereby blocks early hematopoiesis by inducing cell cycle arrest
Sun W et al. RUNX1 overexpression triggers TGF-β signaling to upregulate p15 and thereby blocks early hematopoiesis by inducing cell cycle arrest. . 2022-04-00. Pubmed ID: 35131736; DOI: 10.1016/j.scr.2022.102694 WAe001-A 2022-04-00 2022-04-00 PubMed: 35131736 DOI: 10.1016/j.scr.2022.102694Associated cell lines:
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Sun W, Hu X, Wang L, Ma Y, Zhang X, Zhang R, Zhao L, Ren J, Yang L, Wang G
Generation of iPSC line from urine cells of hemophilia A with F8 (p. R814X) mutation
Sun W et al. Generation of iPSC line from urine cells of hemophilia A with F8 (p. R814X) mutation. . 2022-04-00. Pubmed ID: 35123343; DOI: 10.1016/j.scr.2022.102682 SXMUi002-A 2022-04-00 2022-04-00 PubMed: 35123343 DOI: 10.1016/j.scr.2022.102682Associated cell lines:
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Gilmozzi V, Gentile G, Riekschnitz DA, Volpato CB, Di Segni M, Silipigni R, Pramstaller PP, Hicks AA, Pichler I, Zanon A
Generation of an induced pluripotent stem cell line (EURACi014-A) from a Parkinson's disease patient with an A53T mutation in the SNCA gene by an integration-free reprogramming method
Gilmozzi V et al. Generation of an induced pluripotent stem cell line (EURACi014-A) from a Parkinson's disease patient with an A53T mutation in the SNCA gene by an integration-free reprogramming method. . 2022-04-00. Pubmed ID: 35189566; DOI: 10.1016/j.scr.2022.102713 EURACi005-AEURACi014-A 2022-04-00 2022-04-00 PubMed: 35189566 DOI: 10.1016/j.scr.2022.102713Associated cell lines:
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Mittal N, Dave J, Harakalova M, van Tintelen JP, Asselbergs FW, Doevendans PA, Costa KD, Turnbull IC, Stillitano F
Generation of human induced pluripotent stem cell (iPSC) lines derived from five patients carrying the pathogenic phospholamban-R14del (PLN-R14del) variant and three non-carrier family members
Mittal N et al. Generation of human induced pluripotent stem cell (iPSC) lines derived from five patients carrying the pathogenic phospholamban-R14del (PLN-R14del) variant and three non-carrier family members. . 2022-04-00. Pubmed ID: 35247838; DOI: 10.1016/j.scr.2022.102737 ISMMSi044-AISMMSi045-AISMMSi046-AISMMSi047-AISMMSi048-AISMMSi049-AISMMSi050-AISMMSi051-A 2022-04-00 2022-04-00 PubMed: 35247838 DOI: 10.1016/j.scr.2022.102737Associated cell lines:
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Tian Y, Shi Z, Liao Y, Cai J, Li W, Li X, Chen WX
Generation of an induced pluripotent stem cell line (GWCMCi005-A) from a patient with Lennox-Gastaut syndrome carrying TANC2 Gln1441Ter mutation
Tian Y et al. Generation of an induced pluripotent stem cell line (GWCMCi005-A) from a patient with Lennox-Gastaut syndrome carrying TANC2 Gln1441Ter mutation. . 2022-04-00. Pubmed ID: 35066241; DOI: 10.1016/j.scr.2022.102667 GWCMCi005-A 2022-04-00 2022-04-00 PubMed: 35066241 DOI: 10.1016/j.scr.2022.102667Associated cell lines:
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Gizon M, Duboscq-Bidot L, El Kassar L, Bobin P, Ader F, Giraud-Triboult K, Charron P, Villard E, Fontaine V, Neyroud N
Generation of a heterozygous SCN5A knockout human induced pluripotent stem cell line by CRISPR/Cas9 edition
Gizon M et al. Generation of a heterozygous SCN5A knockout human induced pluripotent stem cell line by CRISPR/Cas9 edition. . 2022-04-00. Pubmed ID: 35093717; DOI: 10.1016/j.scr.2022.102680 ICANi002-AICANi002-A-2 2022-04-00 2022-04-00 PubMed: 35093717 DOI: 10.1016/j.scr.2022.102680Associated cell lines:
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Bchetnia M, Martineau L, Racine V, Powell J, McCuaig C, Morin C, Dupérée A, Gros-Louis F, Laprise C
Generation of three induced pluripotent stem cell lines (UQACi003-A, UQACi004-A, and UQACi006-A) from three patients with KRT5 epidermolysis bullosa simplex mutations
Bchetnia M et al. Generation of three induced pluripotent stem cell lines (UQACi003-A, UQACi004-A, and UQACi006-A) from three patients with KRT5 epidermolysis bullosa simplex mutations. . 2022-04-00. Pubmed ID: 35247839; DOI: 10.1016/j.scr.2022.102726 UQACi003-AUQACi004-AUQACi006-A 2022-04-00 2022-04-00 PubMed: 35247839 DOI: 10.1016/j.scr.2022.102726Associated cell lines:
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Hunter ZL, Leeson HC, Shaker MR, Wolvetang EJ, Vadlamudi L
Human induced pluripotent stem cells generated from epilepsy patients for use as in vitro models for drug screening
Hunter ZL et al. Human induced pluripotent stem cells generated from epilepsy patients for use as in vitro models for drug screening. . 2022-04-00. Pubmed ID: 35074713; DOI: 10.1016/j.scr.2022.102673 AIBNi007-AAIBNi008-AAIBNi009-AAIBNi010-AAIBNi011-AAIBNi012-A 2022-04-00 2022-04-00 PubMed: 35074713 DOI: 10.1016/j.scr.2022.102673Associated cell lines:
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Liang L, Xue Y, Su C, Wang J, Chen L, Su T, Ke J, Xie L, Cui Z, Yu Q, Chan HF, Zhong J, Guo Y, Chen J
Establishment of iPS cell line (KLRMMEi002-A) by reprogramming peripheral blood mononuclear cells from a patient with USH2A-associated Usher syndrome
Liang L et al. Establishment of iPS cell line (KLRMMEi002-A) by reprogramming peripheral blood mononuclear cells from a patient with USH2A-associated Usher syndrome. . 2022-04-00. Pubmed ID: 35152177; DOI: 10.1016/j.scr.2022.102699 KLRMMEi002-A 2022-04-00 2022-04-00 PubMed: 35152177 DOI: 10.1016/j.scr.2022.102699Associated cell lines:
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Zakharova IS, Shevchenko AI, Tmoyan NA, Elisaphenko EA, Kalinin AP, Sleptcov AA, Nazarenko MS, Ezhov MV, Kukharchuk VV, Parfyonova YV, Zakian SM
Induced pluripotent stem cell line ICGi037-A, obtained by reprogramming peripheral blood mononuclear cells from a patient with familial hypercholesterolemia due to heterozygous p.Trp443Arg mutations in LDLR
Zakharova IS et al. Induced pluripotent stem cell line ICGi037-A, obtained by reprogramming peripheral blood mononuclear cells from a patient with familial hypercholesterolemia due to heterozygous p.Trp443Arg mutations in LDLR. . 2022-04-00. Pubmed ID: 35152179; DOI: 10.1016/j.scr.2022.102703 ICGi037-A 2022-04-00 2022-04-00 PubMed: 35152179 DOI: 10.1016/j.scr.2022.102703Associated cell lines:
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Sun L, Zhong J, Wu F, Li F, Yang X, Zeng Z
Establishment of human embryonic stem cell WAe009-A-74 carrying a Long QT syndrome mutation in KCNH2
Sun L et al. Establishment of human embryonic stem cell WAe009-A-74 carrying a Long QT syndrome mutation in KCNH2. . 2022-04-00. Pubmed ID: 35247842; DOI: 10.1016/j.scr.2022.102725 WAe009-AWAe009-A-74 2022-04-00 2022-04-00 PubMed: 35247842 DOI: 10.1016/j.scr.2022.102725Associated cell lines:
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Maurer W, Hartmann N, Argyriou L, Sossalla S, Streckfuss-Bömeke K
Generation of homozygous Na(v)1.8 knock-out iPSC lines by CRISPR Cas9 genome editing to investigate a potential new antiarrhythmic strategy
Maurer W et al. Generation of homozygous Na(v)1.8 knock-out iPSC lines by CRISPR Cas9 genome editing to investigate a potential new antiarrhythmic strategy. . 2022-04-00. Pubmed ID: 35092938; DOI: 10.1016/j.scr.2022.102677 UMGi158-AUMGi158-A-1 2022-04-00 2022-04-00 PubMed: 35092938 DOI: 10.1016/j.scr.2022.102677Associated cell lines:
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Zhu Z, Zhou X, Chen D, Lu K, Lu Y
Effects of feeder cells on proliferation of inducible pluripotent stem cells in chicken
Zhu Z et al. Effects of feeder cells on proliferation of inducible pluripotent stem cells in chicken. . 2022-04-00. Pubmed ID: 34024235; DOI: 10.1080/10520295.2021.1918767 UKBi011-A 2022-04-00 2022-04-00 PubMed: 34024235 DOI: 10.1080/10520295.2021.1918767Associated cell lines:
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Raad S, David A, Chung W, Faure C
Generation of three induced pluripotent stem cells lines from patients with esophageal atresia/tracheoesophageal fistula type C
Raad S et al. Generation of three induced pluripotent stem cells lines from patients with esophageal atresia/tracheoesophageal fistula type C. . 2022-04-00. Pubmed ID: 35193008; DOI: 10.1016/j.scr.2022.102711; PMC: PMC10104726 CHUSJi001-ACHUSJi002-ACHUSJi003-A 2022-04-00 2022-04-00 PubMed: 35193008 DOI: 10.1016/j.scr.2022.102711Associated cell lines:
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Chanprasert C, Promnakhon N, Thongsin N, Suwanpitak S, Plengvidhya N, Yenchitsommanus PT, Jungtrakoon Thamtarana P, Wattanapanitch M
Generation of an induced pluripotent stem cell line (MUSIi014-A) from an affected member of a family with autosomal dominant diabetes carrying p.L475P mutation in ZYG11A gene associated with a cell cycle arrest in beta-cell
Chanprasert C et al. Generation of an induced pluripotent stem cell line (MUSIi014-A) from an affected member of a family with autosomal dominant diabetes carrying p.L475P mutation in ZYG11A gene associated with a cell cycle arrest in beta-cell. . 2022-04-00. Pubmed ID: 35193007; DOI: 10.1016/j.scr.2022.102715 MUSIi014-A 2022-04-00 2022-04-00 PubMed: 35193007 DOI: 10.1016/j.scr.2022.102715Associated cell lines:
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Takahashi M, Furuya N
Evaluation of the Effects of Exposure to Power-Frequency Magnetic Fields on the Differentiation of Hematopoietic Stem/Progenitor Cells Using Human-Induced Pluripotent Stem Cells
Takahashi M et al. Evaluation of the Effects of Exposure to Power-Frequency Magnetic Fields on the Differentiation of Hematopoietic Stem/Progenitor Cells Using Human-Induced Pluripotent Stem Cells. . 2022-04-00. Pubmed ID: 35132646; DOI: 10.1002/bem.22394; PMC: PMC9304145 IMSUTi002-A-1 2022-04-00 2022-04-00 PubMed: 35132646 DOI: 10.1002/bem.22394Associated cell lines:
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Chumchuen S, Satirapod C, Tangprasittipap A, Hongeng S
Establishment of human induced pluripotent stem cell line MUi028-A from normal fetal skin fibroblasts
Chumchuen S et al. Establishment of human induced pluripotent stem cell line MUi028-A from normal fetal skin fibroblasts. . 2022-04-00. Pubmed ID: 35114587; DOI: 10.1016/j.scr.2022.102675 MUi028-A 2022-04-00 2022-04-00 PubMed: 35114587 DOI: 10.1016/j.scr.2022.102675Associated cell lines:
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Zafar F, Nallur Srinivasaraghavan V, Yang Chen M, Alejandra Morato Torres C, Schüle B
Isogenic human SNCA gene dosage induced pluripotent stem cells to model Parkinson's disease
Zafar F et al. Isogenic human SNCA gene dosage induced pluripotent stem cells to model Parkinson's disease. . 2022-04-00. Pubmed ID: 35263701; DOI: 10.1016/j.scr.2022.102733 SUSMi005-ASUSMi005-A-1SUSMi005-A-2SUSMi005-A-3SUSMi005-A-4SUSMi005-A-5 2022-04-00 2022-04-00 PubMed: 35263701 DOI: 10.1016/j.scr.2022.102733Associated cell lines:
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Zhang Y, Shou J, Gu W, Di W, Zhao J, Wang Y, Gu S
Establishment of SIAISi017-A, an induced pluripotent stem cell(iPSC)line from a healthy 25-year-old Chinese Hui
Zhang Y et al. Establishment of SIAISi017-A, an induced pluripotent stem cell(iPSC)line from a healthy 25-year-old Chinese Hui. . 2022-04-00. Pubmed ID: 35093714; DOI: 10.1016/j.scr.2021.102645 SIAISi017-A 2022-04-00 2022-04-00 PubMed: 35093714 DOI: 10.1016/j.scr.2021.102645Associated cell lines:
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Xu Y, Wang X, Qiu T, Wang J, Wang Y, Wu B, Zhou Y
Generation of an induced pluripotent stem cell line (FDCHI007-A) derived from a patient with developmental and epileptic encephalopathy Type 31 carrying heterozygous c.545C > A mutation in DNM1 gene
Xu Y et al. Generation of an induced pluripotent stem cell line (FDCHI007-A) derived from a patient with developmental and epileptic encephalopathy Type 31 carrying heterozygous c.545C > A mutation in DNM1 gene. . 2022-04-00. Pubmed ID: 35184021; DOI: 10.1016/j.scr.2022.102709 FDCHi007-A 2022-04-00 2022-04-00 PubMed: 35184021 DOI: 10.1016/j.scr.2022.102709Associated cell lines:
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Boonkaew B, Suwanpitak S, Pattanapanyasat K, Sermsathanasawadi N, Wattanapanitch M
Efficient generation of endothelial cells from induced pluripotent stem cells derived from a patient with peripheral arterial disease
Boonkaew B et al. Efficient generation of endothelial cells from induced pluripotent stem cells derived from a patient with peripheral arterial disease. . 2022-04-00. Pubmed ID: 35072793; DOI: 10.1007/s00441-022-03576-2 MUSIi001-AMUSIi011-AMUSIi011-BMUSIi001-A-1 2022-04-00 2022-04-00 PubMed: 35072793 DOI: 10.1007/s00441-022-03576-2Associated cell lines:
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Lu X, Mai J, Liu L, Chen X, Shen Y
Generation of an induced pluripotent stem cell line ATCi002-A from a two-year-old chinese boy with Keipert syndrome
Lu X et al. Generation of an induced pluripotent stem cell line ATCi002-A from a two-year-old chinese boy with Keipert syndrome. . 2022-04-00. Pubmed ID: 35168097; DOI: 10.1016/j.scr.2022.102706 ATCi002-A 2022-04-00 2022-04-00 PubMed: 35168097 DOI: 10.1016/j.scr.2022.102706Associated cell lines:
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Zhang F, Meier AB, Lipp P, Laugwitz KL, Dorn T, Moretti A
Generation of heterozygous (MRli003-A-3) and homozygous (MRli003-A-4) TRPM4 knockout human iPSC lines
Zhang F et al. Generation of heterozygous (MRli003-A-3) and homozygous (MRli003-A-4) TRPM4 knockout human iPSC lines. . 2022-04-00. Pubmed ID: 35245852; DOI: 10.1016/j.scr.2022.102731 MRIi003-AMRIi003-A-3MRIi003-A-4 2022-04-00 2022-04-00 PubMed: 35245852 DOI: 10.1016/j.scr.2022.102731Associated cell lines:
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Zhang Y, Shou J, Gu W, Di W, Zhao J, Wang Y, Gu S
Establishment of SIAISi018-A, an induced pluripotent stem cell (iPSC) line from a healthy 45-year-old Chinese Han
Zhang Y et al. Establishment of SIAISi018-A, an induced pluripotent stem cell (iPSC) line from a healthy 45-year-old Chinese Han. . 2022-04-00. Pubmed ID: 35124538; DOI: 10.1016/j.scr.2022.102659 SIAISi018-A 2022-04-00 2022-04-00 PubMed: 35124538 DOI: 10.1016/j.scr.2022.102659Associated cell lines:
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Martínez-Moreno R, Pérez-Serra A, Carreras D, Aran B, Kuebler B, Brugada R, Scornik FS, Pérez GJ, Selga E
Generation of an induced pluripotent stem cell line from a healthy Caucasian male
Martínez-Moreno R et al. Generation of an induced pluripotent stem cell line from a healthy Caucasian male. . 2022-04-00. Pubmed ID: 35231795; DOI: 10.1016/j.scr.2022.102717 IDIBGIi001-A 2022-04-00 2022-04-00 PubMed: 35231795 DOI: 10.1016/j.scr.2022.102717Associated cell lines:
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Ma Y, Shang S, Shi M, Yang Y, Li Q, Bai XY
Establishment of the induced pluripotent stem cell line PLAFMCi006-A from peripheral blood mononuclear cells of polycystic kidney disease patients with PKD2 gene mutation
Ma Y et al. Establishment of the induced pluripotent stem cell line PLAFMCi006-A from peripheral blood mononuclear cells of polycystic kidney disease patients with PKD2 gene mutation. . 2022-04-00. Pubmed ID: 35091308; DOI: 10.1016/j.scr.2022.102681 PUMCHi004-ACPGHi006-A 2022-04-00 2022-04-00 PubMed: 35091308 DOI: 10.1016/j.scr.2022.102681Associated cell lines:
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Zakharova IS, Shevchenko AI, Tmoyan NA, Elisaphenko EA, Zubkova ES, Sleptcov AA, Nazarenko MS, Ezhov MV, Kukharchuk VV, Parfyonova YV, Zakian SM
Induced pluripotent stem cell line ICGi038-A, obtained by reprogramming peripheral blood mononuclear cells from a patient with familial hypercholesterolemia due to compound heterozygous c.1246C > T/c.940 + 3_940 + 6del mutations in LDLR
Zakharova IS et al. Induced pluripotent stem cell line ICGi038-A, obtained by reprogramming peripheral blood mononuclear cells from a patient with familial hypercholesterolemia due to compound heterozygous c.1246C > T/c.940 + 3_940 + 6del mutations in LDLR. . 2022-04-00. Pubmed ID: 35152178; DOI: 10.1016/j.scr.2022.102702 ICGi038-A 2022-04-00 2022-04-00 PubMed: 35152178 DOI: 10.1016/j.scr.2022.102702Associated cell lines:
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Kamiya D, Yamashita T, Akaboshi T, Yamaguchi Y, Toyooka Y, Ikeya M
Generation of human GAPDH knock-in reporter iPSC lines for stable expression of tdTomato in pluripotent and differentiated culture conditions
Kamiya D et al. Generation of human GAPDH knock-in reporter iPSC lines for stable expression of tdTomato in pluripotent and differentiated culture conditions. . 2022-04-00. Pubmed ID: 35176664; DOI: 10.1016/j.scr.2022.102704 KUIMSi012-AKUIMSi012-A-1KUIMSi012-A-2 2022-04-00 2022-04-00 PubMed: 35176664 DOI: 10.1016/j.scr.2022.102704Associated cell lines:
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Lahm H, Heinrich P, Zierler E, Dzilic E, Neb I, Luzius T, Doppler SA, Schneider S, Lange R, Krane M, Dreßen M
Generation of a CRISPR/Cas edited human induced pluripotent stem cell line DHMi005-A-1 carrying a patient-specific disease-causing point mutation in the TBX5 gene
Lahm H et al. Generation of a CRISPR/Cas edited human induced pluripotent stem cell line DHMi005-A-1 carrying a patient-specific disease-causing point mutation in the TBX5 gene. . 2022-04-00. Pubmed ID: 35121196; DOI: 10.1016/j.scr.2022.102691 DHMi005-ADHMi005-A-1 2022-04-00 2022-04-00 PubMed: 35121196 DOI: 10.1016/j.scr.2022.102691Associated cell lines:
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Zhao X, Cao J, Li X, Liu M, Liu Y, Dong J, Zhao X
A heterozygous MYBPC3 (c. 772+1G > A) mutant human induced pluripotent stem cell line (ZZUNEUi025-A) generated from a male patient with hypertrophic cardiomyopathy
Zhao X et al. A heterozygous MYBPC3 (c. 772+1G > A) mutant human induced pluripotent stem cell line (ZZUNEUi025-A) generated from a male patient with hypertrophic cardiomyopathy. . 2022-04-00. Pubmed ID: 35257994; DOI: 10.1016/j.scr.2022.102722 ZZUNEUi025-A 2022-04-00 2022-04-00 PubMed: 35257994 DOI: 10.1016/j.scr.2022.102722Associated cell lines:
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Wang H, Luo Y, Li J, Guan J, Yang S, Wang Q
Generation of a gene corrected human isogenic iPSC line (CPGHi001-A-1) from a hearing loss patient with the TMC1 p.M418K mutation using CRISPR/Cas9
Wang H et al. Generation of a gene corrected human isogenic iPSC line (CPGHi001-A-1) from a hearing loss patient with the TMC1 p.M418K mutation using CRISPR/Cas9. . 2022-04-00. Pubmed ID: 35247837; DOI: 10.1016/j.scr.2022.102736 CPGHi001-ACPGHi001-A-1 2022-04-00 2022-04-00 PubMed: 35247837 DOI: 10.1016/j.scr.2022.102736Associated cell lines:
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Cha YJ, Jeon SB, Oh J, Lee ST, Kim S, Kim H, Choi J, Choi HK, Won D, Choi JR, Kim SJ, Park SW, Kang SM, Lee SH
Derivation of YCMi005-A, a human-induced pluripotent stem cell line, from a patient with dilated cardiomyopathy carrying missense variant in TPM1 (p. Glu192Lys)
Cha YJ et al. Derivation of YCMi005-A, a human-induced pluripotent stem cell line, from a patient with dilated cardiomyopathy carrying missense variant in TPM1 (p. Glu192Lys). . 2022-04-00. Pubmed ID: 35176663; DOI: 10.1016/j.scr.2022.102707 YCMi005-A 2022-04-00 2022-04-00 PubMed: 35176663 DOI: 10.1016/j.scr.2022.102707Associated cell lines:
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Sanjurjo-Soriano C, Erkilic N, Vache C, Dubois G, Roux AF, Meunier I, Kalatzis V
Generation of a human iPSC line, INMi005-A, from a patient with non-syndromic USH2A-associated retinitis pigmentosa
Sanjurjo-Soriano C et al. Generation of a human iPSC line, INMi005-A, from a patient with non-syndromic USH2A-associated retinitis pigmentosa. . 2022-04-00. Pubmed ID: 35248879; DOI: 10.1016/j.scr.2022.102738 INMi005-A 2022-04-00 2022-04-00 PubMed: 35248879 DOI: 10.1016/j.scr.2022.102738Associated cell lines:
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Jia G, Cui Y, Shi L, Luan J, Wang J, Han J
Generation of a transgene-free induced pluripotent stem cell line (SMBCi011-A) from a patient with Prader-Willi syndrome
Jia G et al. Generation of a transgene-free induced pluripotent stem cell line (SMBCi011-A) from a patient with Prader-Willi syndrome. . 2022-04-00. Pubmed ID: 35203049; DOI: 10.1016/j.scr.2022.102695 SMBCi006-ASMBCi011-A 2022-04-00 2022-04-00 PubMed: 35203049 DOI: 10.1016/j.scr.2022.102695Associated cell lines:
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Zhang L, Ma XJ, Fei YY, Han HT, Xu J, Cheng L, Li X
Stem cell therapy in liver regeneration: Focus on mesenchymal stem cells and induced pluripotent stem cells
Zhang L et al. Stem cell therapy in liver regeneration: Focus on mesenchymal stem cells and induced pluripotent stem cells. . 2022-04-00. Pubmed ID: 34597754; DOI: 10.1016/j.pharmthera.2021.108004 ZZUNEUi005-A 2022-04-00 2022-04-00 PubMed: 34597754 DOI: 10.1016/j.pharmthera.2021.108004Associated cell lines:
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Jin M, Wang D, Li G, Lin J, Lin X, Wang N
Generation and characterization of an induced pluripotent stem cell line (FJMUNi001-A) from a patient with Duchenne muscular dystrophy carrying c.4518 + 512 T > A variant in the DMD gene
Jin M et al. Generation and characterization of an induced pluripotent stem cell line (FJMUNi001-A) from a patient with Duchenne muscular dystrophy carrying c.4518 + 512 T > A variant in the DMD gene. . 2022-04-00. Pubmed ID: 35247844; DOI: 10.1016/j.scr.2022.102718 FJMUNi001-A 2022-04-00 2022-04-00 PubMed: 35247844 DOI: 10.1016/j.scr.2022.102718Associated cell lines:
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Khor W, Hwang TC, Wang CC, Yarmishyn AA, Yeh JT, Chiou SH, Chou SJ
Generation of human induced pluripotent stem cells from cystic fibrosis patient carrying nonsense mutation (p.S308X) in CFTR gene
Khor W et al. Generation of human induced pluripotent stem cells from cystic fibrosis patient carrying nonsense mutation (p.S308X) in CFTR gene. . 2022-04-00. Pubmed ID: 35091309; DOI: 10.1016/j.scr.2022.102683 TVGHi008-A 2022-04-00 2022-04-00 PubMed: 35091309 DOI: 10.1016/j.scr.2022.102683Associated cell lines:
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Yamashita T, Kamiya D, Kawaraichi N, Toyokawa H, Akaboshi T, Ikeya M, Toyooka Y
Generation of a human SOX10 knock-in reporter iPSC line for visualization of neural crest cell differentiation
Yamashita T et al. Generation of a human SOX10 knock-in reporter iPSC line for visualization of neural crest cell differentiation. . 2022-04-00. Pubmed ID: 35144211; DOI: 10.1016/j.scr.2022.102696 KUIMSi012-A-3 2022-04-00 2022-04-00 PubMed: 35144211 DOI: 10.1016/j.scr.2022.102696Associated cell lines:
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Zhang JW, Cheng QC, Ding HR, Zhang L, Xu YY, Sang XT, Zhao HT, Zhang WG, Lu X
Letter to the editor: The role of aquaporin 9 in modeling of ornithine transcarbamylase deficiency
Zhang JW et al. Letter to the editor: The role of aquaporin 9 in modeling of ornithine transcarbamylase deficiency. . 2022-04-00. Pubmed ID: 34929066; DOI: 10.1002/hep.32293 SDQLCHi036-A 2022-04-00 2022-04-00 PubMed: 34929066 DOI: 10.1002/hep.32293Associated cell lines:
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Simons E, Nijak A, Loeys B, Alaerts M
Generation of two induced pluripotent stem cell (iPSC) lines (BBANTWi006-A, BBANTWi007-A) from Brugada syndrome patients carrying an SCN5A mutation
Simons E et al. Generation of two induced pluripotent stem cell (iPSC) lines (BBANTWi006-A, BBANTWi007-A) from Brugada syndrome patients carrying an SCN5A mutation. . 2022-04-00. Pubmed ID: 35247843; DOI: 10.1016/j.scr.2022.102719; PMC: PMC8924004 BBANTWi006-ABBANTWi007-A 2022-04-00 2022-04-00 PubMed: 35247843 DOI: 10.1016/j.scr.2022.102719Associated cell lines:
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Zheng F, Chen L, Qiu L, Lin L, Lin X, He Q, Wang L, Ye Z, Lin M, Wang Z
Reprogramming of adult human peripheral blood mononuclear cells into hiPSCs from two patients with facioscapulohumeral muscular dystrophy type 1
Zheng F et al. Reprogramming of adult human peripheral blood mononuclear cells into hiPSCs from two patients with facioscapulohumeral muscular dystrophy type 1. . 2022-04-00. Pubmed ID: 35093715; DOI: 10.1016/j.scr.2022.102678 FMUFAHi001-AFMUFAHi002-A 2022-04-00 2022-04-00 PubMed: 35093715 DOI: 10.1016/j.scr.2022.102678Associated cell lines:
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Sun Z, Wu S, Zhu T, Wei X, Han X, Zou X, Sui R
Generation of a human induced pluripotent stem cell line PUMCHi019-A from a dominant optic atrophy patient with an OPA1 mutation
Sun Z et al. Generation of a human induced pluripotent stem cell line PUMCHi019-A from a dominant optic atrophy patient with an OPA1 mutation. . 2022-04-00. Pubmed ID: 35152176; DOI: 10.1016/j.scr.2022.102705 PUMCHi019-A 2022-04-00 2022-04-00 PubMed: 35152176 DOI: 10.1016/j.scr.2022.102705Associated cell lines:
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Ricci Signorini ME, Szepes M, Melchert A, Bakar M, Merkert S, Haase A, Göhring G, Martin U, Gruh I
Generation of human induced pluripotent stem cell lines encoding for genetically encoded calcium indicators RCaMP1h and GCaMP6f
Ricci Signorini ME et al. Generation of human induced pluripotent stem cell lines encoding for genetically encoded calcium indicators RCaMP1h and GCaMP6f. . 2022-04-00. Pubmed ID: 35152180; DOI: 10.1016/j.scr.2022.102697 MHHi001-AMHHi001-A-8MHHi001-A-9 2022-04-00 2022-04-00 PubMed: 35152180 DOI: 10.1016/j.scr.2022.102697Associated cell lines:
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Zhang Y, Zhu J, Dai Y, Wang L, Liu R, Guo X
Generation of a heterozygous FUS-Q290X knock in human embryonic stem cell line (WAe009-A-83) using CRISPR/Cas9 system
Zhang Y et al. Generation of a heterozygous FUS-Q290X knock in human embryonic stem cell line (WAe009-A-83) using CRISPR/Cas9 system. . 2022-04-00. Pubmed ID: 35247836; DOI: 10.1016/j.scr.2022.102734 WAe009-AWAe009-A-83 2022-04-00 2022-04-00 PubMed: 35247836 DOI: 10.1016/j.scr.2022.102734Associated cell lines:
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Chiu W, Li A, Wang T, Li W, Zhang X
Generation of a MSX1 knockout human embryonic stem cell line using CRISPR/Cas9 technology
Chiu W et al. Generation of a MSX1 knockout human embryonic stem cell line using CRISPR/Cas9 technology. . 2022-04-00. Pubmed ID: 35247841; DOI: 10.1016/j.scr.2022.102729 WAe009-A-81 2022-04-00 2022-04-00 PubMed: 35247841 DOI: 10.1016/j.scr.2022.102729Associated cell lines:
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Wei C, Lu X, Zou Q, Gong S, Chen Y, Lyu J, Jia J
Generation and characterization of a human induced pluripotent stem cell line (XWHNi001-A) derived from an Alzheimer's disease patient with mutation in the APP gene
Wei C et al. Generation and characterization of a human induced pluripotent stem cell line (XWHNi001-A) derived from an Alzheimer's disease patient with mutation in the APP gene. . 2022-04-00. Pubmed ID: 35149456; DOI: 10.1016/j.scr.2022.102690 XWHNi001-A 2022-04-00 2022-04-00 PubMed: 35149456 DOI: 10.1016/j.scr.2022.102690Associated cell lines:
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Colombani S, Bernardin AA, Vincenti M, Amédro P, Desprat R, Bernex F, Lemaitre JM, Pasquié JL, Lacampagne A, Meli AC
Generation of catecholaminergic polymorphic ventricular tachycardia patient-specific induced pluripotent stem cell line
Colombani S et al. Generation of catecholaminergic polymorphic ventricular tachycardia patient-specific induced pluripotent stem cell line. . 2022-04-00. Pubmed ID: 35245853; DOI: 10.1016/j.scr.2022.102727 REGUi003-AINSRMi011-A 2022-04-00 2022-04-00 PubMed: 35245853 DOI: 10.1016/j.scr.2022.102727Associated cell lines:
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Ma Y, Sun W, Liu X, Ren J, Zhang X, Zhang R, Zhao L, Yang L, Wang G
Generation an induced pluripotent stem cell line SXMUi001-A derived from a hemophilia B patient carries variant F9 c.223C>T(p.R75X)
Ma Y et al. Generation an induced pluripotent stem cell line SXMUi001-A derived from a hemophilia B patient carries variant F9 c.223C>T(p.R75X). . 2022-04-00. Pubmed ID: 35121195; DOI: 10.1016/j.scr.2022.102684 SXMUi001-A 2022-04-00 2022-04-00 PubMed: 35121195 DOI: 10.1016/j.scr.2022.102684Associated cell lines:
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Lou J, Chen H, Huang S, Chen P, Yu Y, Chen F
Update on risk factors and biomarkers of sudden unexplained cardiac death
Lou J et al. Update on risk factors and biomarkers of sudden unexplained cardiac death. . 2022-04-00. Pubmed ID: 35272106; DOI: 10.1016/j.jflm.2022.102332 PSMi003-ANUIGi005-ANUIGi005-BNUIGi005-CNUIGi006-ANUIGi006-BNUIGi006-CNUIGi007-ANUIGi007-BHDZi001-A 2022-04-00 2022-04-00 PubMed: 35272106 DOI: 10.1016/j.jflm.2022.102332Associated cell lines:
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Vázquez-Domínguez I, Kwint M, Kroes HY, Albert S, O'Gorman L, Gilissen C, Cremers FPM, Collin RWJ, Roosing S, Garanto A
Generation of a patient-derived induced pluripotent cell line (SCTCi016-A) carrying a homozygous variant in RPE65
Vázquez-Domínguez I et al. Generation of a patient-derived induced pluripotent cell line (SCTCi016-A) carrying a homozygous variant in RPE65. . 2022-04-00. Pubmed ID: 35121194; DOI: 10.1016/j.scr.2022.102689 SCTCi016-A 2022-04-00 2022-04-00 PubMed: 35121194 DOI: 10.1016/j.scr.2022.102689Associated cell lines:
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Ishikawa KI, Ishiguro M, Li Y, Nishioka K, Hattori N, Akamatsu W
Generation of three hiPSC clones from a Parkinson's disease patient with a heterozygous variant of VPS35 p.D620N
Ishikawa KI et al. Generation of three hiPSC clones from a Parkinson's disease patient with a heterozygous variant of VPS35 p.D620N. . 2022-04-00. Pubmed ID: 35247840; DOI: 10.1016/j.scr.2022.102739 JUCGRMi001-AJUCGRMi001-BJUCGRMi001-C 2022-04-00 2022-04-00 PubMed: 35247840 DOI: 10.1016/j.scr.2022.102739Associated cell lines:
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Kang B, Cong Z, Duan J, Liu K, Wang Y
Generation of a GFI1-flag knock-in human embryonic stem cell line using CRISPR-Cas9 technology
Kang B et al. Generation of a GFI1-flag knock-in human embryonic stem cell line using CRISPR-Cas9 technology. . 2022-04-00. Pubmed ID: 35248880; DOI: 10.1016/j.scr.2022.102724 JLUe003-A 2022-04-00 2022-04-00 PubMed: 35248880 DOI: 10.1016/j.scr.2022.102724Associated cell lines:
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Kim JH, Kang KW, Lee BH, Park Y, Jung Sung H, Kim BS
A human pluripotent stem cell line KUMi004-A generated from a patient with chronic lymphocytic leukemia
Kim JH et al. A human pluripotent stem cell line KUMi004-A generated from a patient with chronic lymphocytic leukemia. . 2022-04-00. Pubmed ID: 35066240; DOI: 10.1016/j.scr.2022.102668 KUMi004-A 2022-04-00 2022-04-00 PubMed: 35066240 DOI: 10.1016/j.scr.2022.102668Associated cell lines:
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Korneck M, Wiora L, Schöls L, Hauser S
Generation of two SPAST knockout human induced pluripotent stem cell lines to create a model for Hereditary Spastic Paraplegia type 4
Korneck M et al. Generation of two SPAST knockout human induced pluripotent stem cell lines to create a model for Hereditary Spastic Paraplegia type 4. . 2022-04-00. Pubmed ID: 35248878; DOI: 10.1016/j.scr.2022.102741 HIHCNi006-AHIHCNi006-BHIHCNi006-CHIHCNi006-A-1HIHCNi006-A-2 2022-04-00 2022-04-00 PubMed: 35248878 DOI: 10.1016/j.scr.2022.102741Associated cell lines:
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Chesshyre M, Ridout D, Hashimoto Y, Ookubo Y, Torelli S, Maresh K, Ricotti V, Abbott L, Gupta VA, Main M, Ferrari G, Kowala A, Lin YY, Tedesco FS, Scoto M, Baranello G, Manzur A, Aoki Y, Muntoni F
Investigating the role of dystrophin isoform deficiency in motor function in Duchenne muscular dystrophy
Chesshyre M et al. Investigating the role of dystrophin isoform deficiency in motor function in Duchenne muscular dystrophy. . 2022-04-00. Pubmed ID: 35083887; DOI: 10.1002/jcsm.12914; PMC: PMC8977977 UCLi011-A 2022-04-00 2022-04-00 PubMed: 35083887 DOI: 10.1002/jcsm.12914Associated cell lines:
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Jagtap S, Sowmithra, Yadav R, Pal PK, Datta I
Generation of induced pluripotent stem cells (NIMHi004-A, NIMHi005-A and NIMHi006-A) from healthy individuals of Indian ethnicity with no mutation for Parkinson's disease related genes
Jagtap S et al. Generation of induced pluripotent stem cells (NIMHi004-A, NIMHi005-A and NIMHi006-A) from healthy individuals of Indian ethnicity with no mutation for Parkinson's disease related genes. . 2022-04-00. Pubmed ID: 35220026; DOI: 10.1016/j.scr.2022.102716 NIMHi001-ANIMHi002-ANIMHi003-ANIMHi004-ANIMHi005-ANIMHi006-A 2022-04-00 2022-04-00 PubMed: 35220026 DOI: 10.1016/j.scr.2022.102716Associated cell lines:
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Castelo Rueda MP, Gilmozzi V, Riekschnitz DA, Di Segni M, Silipigni R, Pramstaller PP, Hicks AA, Pichler I, Zanon A
Generation and characterization of induced pluripotent stem cell (iPSC) lines of two asymptomatic individuals carrying a heterozygous exon 7 deletion in Parkin (PRKN) and two non-carriers from the same family
Castelo Rueda MP et al. Generation and characterization of induced pluripotent stem cell (iPSC) lines of two asymptomatic individuals carrying a heterozygous exon 7 deletion in Parkin (PRKN) and two non-carriers from the same family. . 2022-04-00. Pubmed ID: 35121197; DOI: 10.1016/j.scr.2022.102692 EURACi005-AEURACi010-AEURACi011-AEURACi012-AEURACi013-A 2022-04-00 2022-04-00 PubMed: 35121197 DOI: 10.1016/j.scr.2022.102692Associated cell lines:
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de Toledo MAS, Fu X, Kluge F, Götz K, Schmitz S, Wanek P, Schüler HM, Pannen K, Chatain N, Koschmieder S, Brümmendorf TH, Zenke M
CRISPR/Cas9-engineered human ES cells harboring heterozygous and homozygous c-KIT knockout
de Toledo MAS et al. CRISPR/Cas9-engineered human ES cells harboring heterozygous and homozygous c-KIT knockout. . 2022-04-00. Pubmed ID: 35279545; DOI: 10.1016/j.scr.2022.102732 ESIBIe003-A-11ESIBIe003-A-12 2022-04-00 2022-04-00 PubMed: 35279545 DOI: 10.1016/j.scr.2022.102732Associated cell lines:
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Schuster J, de Guidi C, Tripathi R, Klar J, Dahl N
Generation of a human iPSC line (UUIGPi015-A) from a patient with Dravet syndrome and a 2.9 Mb deletion spanning SCN1A on chromosome 2
Schuster J et al. Generation of a human iPSC line (UUIGPi015-A) from a patient with Dravet syndrome and a 2.9 Mb deletion spanning SCN1A on chromosome 2. . 2022-04-00. Pubmed ID: 35203050; DOI: 10.1016/j.scr.2022.102712 UUIGPi015-A 2022-04-00 2022-04-00 PubMed: 35203050 DOI: 10.1016/j.scr.2022.102712Associated cell lines:
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Gong X, Zheng Z, Yang T, Zheng H, Xiao X, Jia N
Generation of an isogenic gene-corrected iPSC line (OGHFUi001-A-1) from a type 1 early infantile epileptic encephalopathy (EIEE1) patient with a hemizygous R330L mutation in the ARX gene
Gong X et al. Generation of an isogenic gene-corrected iPSC line (OGHFUi001-A-1) from a type 1 early infantile epileptic encephalopathy (EIEE1) patient with a hemizygous R330L mutation in the ARX gene. . 2022-04-00. Pubmed ID: 35121198; DOI: 10.1016/j.scr.2022.102693 OGHFUi001-AOGHFUi001-A-1 2022-04-00 2022-04-00 PubMed: 35121198 DOI: 10.1016/j.scr.2022.102693Associated cell lines:
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Wang T, Tang W, Zeng Q, Miao S, Pi C, Li Y, Yue W, Yu S
Generation of induced pluripotent stem cell line (FMCPGHi001-A) from a 25-year-old Chinese Han healthy male donor
Wang T et al. Generation of induced pluripotent stem cell line (FMCPGHi001-A) from a 25-year-old Chinese Han healthy male donor. . 2022-04-00. Pubmed ID: 35247846; DOI: 10.1016/j.scr.2022.102735 FMCPGHi001-A 2022-04-00 2022-04-00 PubMed: 35247846 DOI: 10.1016/j.scr.2022.102735Associated cell lines:
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Ni P, Wang H, Cai J, Ran J, Jiang Y, Zhao L, Wei J, Ni R, Wang Y, Ma X, Wang Q, Guo W, Li T
Generation and characterization of human-derived iPSC lines from one pair of dizygotic twins discordant for schizophrenia
Ni P et al. Generation and characterization of human-derived iPSC lines from one pair of dizygotic twins discordant for schizophrenia. . 2022-04-00. Pubmed ID: 35182860; DOI: 10.1016/j.scr.2022.102710 WCHi001-AWCHi003-A 2022-04-00 2022-04-00 PubMed: 35182860 DOI: 10.1016/j.scr.2022.102710 -
Lu X, Wang W, Liu Y, Song N, Li M, Mu X, Zhang N, Chen Q, Jiang L, Kong X, Sun P, Tong J, Zhang Y, Li J, Ma S, Han F
Establishment and characterization of human induced pluripotent stem cell line from a Parkinson's disease patient harboring VPS13A gene mutation
Lu X et al. Establishment and characterization of human induced pluripotent stem cell line from a Parkinson's disease patient harboring VPS13A gene mutation. . 2022-04-00. Pubmed ID: 35093716; DOI: 10.1016/j.scr.2022.102685 LCPHi002-A 2022-04-00 2022-04-00 PubMed: 35093716 DOI: 10.1016/j.scr.2022.102685Associated cell lines:
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Pornsukjantra T, Kangboonruang K, Tong-Ngam P, Tim-Aroon T, Wattanasirichaigoon D, Anurathapan U, Hongeng S, Tubsuwan A, Bhukhai K, Asavapanumas N
A generation of human induced pluripotent stem cell line (MUi031-A) from a type-3 Gaucher disease patient carrying homozygous mutation on GBA1 gene
Pornsukjantra T et al. A generation of human induced pluripotent stem cell line (MUi031-A) from a type-3 Gaucher disease patient carrying homozygous mutation on GBA1 gene. . 2022-04-00. Pubmed ID: 35151019; DOI: 10.1016/j.scr.2022.102698 MUi031-A 2022-04-00 2022-04-00 PubMed: 35151019 DOI: 10.1016/j.scr.2022.102698Associated cell lines:
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Koh H, Zhen X, Kim J, Ha HY, Lee JH
Generation and characterization of human umbilical cord blood-derived induced pluripotent stem cells (KRIBBi005-A)
Koh H et al. Generation and characterization of human umbilical cord blood-derived induced pluripotent stem cells (KRIBBi005-A). . 2022-04-00. Pubmed ID: 35085946; DOI: 10.1016/j.scr.2022.102674 KRIBBi004-AKRIBBi005-A 2022-04-00 2022-04-00 PubMed: 35085946 DOI: 10.1016/j.scr.2022.102674Associated cell lines:
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Ji Y, Lv H, Chen Z, Yu J, Fang S, Li F
Generation of a human induced pluripotent stem cell line (SJTUXHi002-A) from an individual with autism spectrum disorder carrying a heterozygous mutation in GRIA2
Ji Y et al. Generation of a human induced pluripotent stem cell line (SJTUXHi002-A) from an individual with autism spectrum disorder carrying a heterozygous mutation in GRIA2. . 2022-04-00. Pubmed ID: 35134694; DOI: 10.1016/j.scr.2022.102676 SJTUXHi002-A 2022-04-00 2022-04-00 PubMed: 35134694 DOI: 10.1016/j.scr.2022.102676Associated cell lines:
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Laemmle A, Häberle J, Willenbring H
Reply
Laemmle A et al. Reply. . 2022-04-00. Pubmed ID: 34935158; DOI: 10.1002/hep.32290 SDQLCHi036-A 2022-04-00 2022-04-00 PubMed: 34935158 DOI: 10.1002/hep.32290Associated cell lines:
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Xiong Y, Wang Y, Xu M, Liu Y, Jiang H, Jiang Z, Wang J
Establishment of an induced pluripotent stem cell line (JTUi003-A) from a patient with otosclerosis
Xiong Y et al. Establishment of an induced pluripotent stem cell line (JTUi003-A) from a patient with otosclerosis. . 2022-04-00. Pubmed ID: 35063912; DOI: 10.1016/j.scr.2022.102666 JTUi003-A 2022-04-00 2022-04-00 PubMed: 35063912 DOI: 10.1016/j.scr.2022.102666Associated cell lines:
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Bray L, Caillaud A, Girardeau A, Patitucci M, Le May C, Cariou B, Rimbert A
Generation of a GPR146 knockout human induced pluripotent stem cell line (ITXi001-A-1)
Bray L et al. Generation of a GPR146 knockout human induced pluripotent stem cell line (ITXi001-A-1). . 2022-04-00. Pubmed ID: 35247835; DOI: 10.1016/j.scr.2022.102721 ITXi001-AITXi001-A-1 2022-04-00 2022-04-00 PubMed: 35247835 DOI: 10.1016/j.scr.2022.102721Associated cell lines:
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Koolen L, Gagliardi G, Ten Brink SCA, de Breuk A, Heesterbeek TJ, Hoyng CB, Albert S, den Hollander AI
Generation and characterization of human induced pluripotent stem cells (iPSCs) from three patients with age-related macular degeneration carrying rare variants in the CFH gene
Koolen L et al. Generation and characterization of human induced pluripotent stem cells (iPSCs) from three patients with age-related macular degeneration carrying rare variants in the CFH gene. . 2022-04-00. Pubmed ID: 35063911; DOI: 10.1016/j.scr.2022.102669 SCTCi011-ASCTCi012-ASCTCi013-A 2022-04-00 2022-04-00 PubMed: 35063911 DOI: 10.1016/j.scr.2022.102669Associated cell lines:
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Hu X, Mao J, Zhang K, Zhang H, Li D, Zhou B, Shan H, Li B, Pang P
Generation of three lines from multiorgan venous and lymphatic defect syndrome patients
Hu X et al. Generation of three lines from multiorgan venous and lymphatic defect syndrome patients. . 2022-04-00. Pubmed ID: 35091306; DOI: 10.1016/j.scr.2022.102679 SYSUIMi001-ASYSUIMi002-ASYSUIMi003-A 2022-04-00 2022-04-00 PubMed: 35091306 DOI: 10.1016/j.scr.2022.102679Associated cell lines:
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Yu Y, Shen H, Zhu J, Cao X, Li Q, Shao L, Shen Z
Generation of Marfan patient specific iPSCs (ICSSUi001-A) carrying a novel heterozygous mutation in FBN1 gene
Yu Y et al. Generation of Marfan patient specific iPSCs (ICSSUi001-A) carrying a novel heterozygous mutation in FBN1 gene. . 2022-04-00. Pubmed ID: 35231796; DOI: 10.1016/j.scr.2022.102720 ICSSUi001-A 2022-04-00 2022-04-00 PubMed: 35231796 DOI: 10.1016/j.scr.2022.102720Associated cell lines:
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Zhang Y, Fan J, Lu G, Xu G, Lv Q
Generation of the induced pluripotent stem cell line (ZSPHARi001-A) from a patient with recessive dystrophic epidermolysis bullosa carrying compound heterozygous mutation in the COL7A1 gene
Zhang Y et al. Generation of the induced pluripotent stem cell line (ZSPHARi001-A) from a patient with recessive dystrophic epidermolysis bullosa carrying compound heterozygous mutation in the COL7A1 gene. . 2022-04-00. Pubmed ID: 35121199; DOI: 10.1016/j.scr.2022.102672 ZSPHARi001-A 2022-04-00 2022-04-00 PubMed: 35121199 DOI: 10.1016/j.scr.2022.102672Associated cell lines:
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Koolen L, Gagliardi G, Ten Brink SCA, de Breuk A, Heesterbeek TJ, Hoyng CB, Albert S, den Hollander AI
Generation and characterization of human induced pluripotent stem cells (iPSCs) from three individuals without age-related macular degeneration
Koolen L et al. Generation and characterization of human induced pluripotent stem cells (iPSCs) from three individuals without age-related macular degeneration. . 2022-04-00. Pubmed ID: 35078129; DOI: 10.1016/j.scr.2022.102670 SCTCi008-ASCTCi009-ASCTCi010-A 2022-04-00 2022-04-00 PubMed: 35078129 DOI: 10.1016/j.scr.2022.102670Associated cell lines:
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Cimarosti B, Canac R, De Waard S, Girardeau A, Gaignerie A, Derevier A, Forest V, Ronjat M, Le Marec H, Gourraud JB, Lemarchand P, De Waard M, Lamirault G, Gaborit N
Generation of human induced pluripotent stem cell lines from three patients affected by Catecholaminergic Polymorphic ventricular tachycardia (CPVT) carrying heterozygous mutations in RYR2 gene
Cimarosti B et al. Generation of human induced pluripotent stem cell lines from three patients affected by Catecholaminergic Polymorphic ventricular tachycardia (CPVT) carrying heterozygous mutations in RYR2 gene. . 2022-04-00. Pubmed ID: 35101670; DOI: 10.1016/j.scr.2022.102688 ITXi009-AITXi010-AITXi011-A 2022-04-00 2022-04-00 PubMed: 35101670 DOI: 10.1016/j.scr.2022.102688 -
Domingues S, Darle A, Masson Y, Saidani M, Lagoutte E, Bejanariu A, Coutier J, Ayata RE, Bouschbacher M, Peschanski M, Lemaitre G, Baldeschi C
Clinical Grade Human Pluripotent Stem Cell-Derived Engineered Skin Substitutes Promote Keratinocytes Wound Closure In Vitro
Domingues S et al. Clinical Grade Human Pluripotent Stem Cell-Derived Engineered Skin Substitutes Promote Keratinocytes Wound Closure In Vitro. . 2022-03-29. Pubmed ID: 35406716; DOI: 10.3390/cells11071151; PMC: PMC8998132 RCPCMi007-ARCPCMi007-A-1 2022-03-29 2022-03-29 PubMed: 35406716 DOI: 10.3390/cells11071151Associated cell lines:
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Danz K, Höcherl T, Wien SL, Wien L, von Briesen H, Wagner S
Experimental Comparison of Primary and hiPS-Based In Vitro Blood-Brain Barrier Models for Pharmacological Research
Danz K et al. Experimental Comparison of Primary and hiPS-Based In Vitro Blood-Brain Barrier Models for Pharmacological Research. . 2022-03-29. Pubmed ID: 35456571; DOI: 10.3390/pharmaceutics14040737; PMC: PMC9031459 UKKi011-A 2022-03-29 2022-03-29 PubMed: 35456571 DOI: 10.3390/pharmaceutics14040737Associated cell lines:
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Song Y, Li H, Ma S, Zhu M, Lu WJ, Lan F, Cui M
Losartan protects human stem cell-derived cardiomyocytes from angiotensin II-induced alcoholic cardiotoxicity
Song Y et al. Losartan protects human stem cell-derived cardiomyocytes from angiotensin II-induced alcoholic cardiotoxicity. . 2022-03-28. Pubmed ID: 35347130; DOI: 10.1038/s41420-022-00945-2; PMC: PMC8960777 WAe009-AWAe009-A-36 2022-03-28 2022-03-28 PubMed: 35347130 DOI: 10.1038/s41420-022-00945-2Associated cell lines:
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Watt SM, Hua P, Roberts I
Increasing Complexity of Molecular Landscapes in Human Hematopoietic Stem and Progenitor Cells during Development and Aging
Watt SM et al. Increasing Complexity of Molecular Landscapes in Human Hematopoietic Stem and Progenitor Cells during Development and Aging. . 2022-03-27. Pubmed ID: 35409034; DOI: 10.3390/ijms23073675; PMC: PMC8999121 CHOPi001-A 2022-03-27 2022-03-27 PubMed: 35409034 DOI: 10.3390/ijms23073675Associated cell lines:
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Bay C, Bajraktari-Sylejmani G, Haefeli WE, Burhenne J, Weiss J, Sauter M
Functional Characterization of the Solute Carrier LAT-1 (SLC7A5/SLC2A3) in Human Brain Capillary Endothelial Cells with Rapid UPLC-MS/MS Quantification of Intracellular Isotopically Labelled L-Leucine
Bay C et al. Functional Characterization of the Solute Carrier LAT-1 (SLC7A5/SLC2A3) in Human Brain Capillary Endothelial Cells with Rapid UPLC-MS/MS Quantification of Intracellular Isotopically Labelled L-Leucine. . 2022-03-26. Pubmed ID: 35408997; DOI: 10.3390/ijms23073637; PMC: PMC8998838 BIONi010-C 2022-03-26 2022-03-26 PubMed: 35408997 DOI: 10.3390/ijms23073637Associated cell lines:
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Imamura S, Yoshimoto K, Terada S, Takamuro K, Kamei KI
In vitro culture at 39 °C during hepatic maturation of human ES cells facilitates hepatocyte-like cell functions
Imamura S et al. In vitro culture at 39 °C during hepatic maturation of human ES cells facilitates hepatocyte-like cell functions. . 2022-03-25. Pubmed ID: 35338220; DOI: 10.1038/s41598-022-09119-7; PMC: PMC8956733 WAe009-A 2022-03-25 2022-03-25 PubMed: 35338220 DOI: 10.1038/s41598-022-09119-7Associated cell lines:
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Boutaud L, Michael M, Banal C, Calderon D, Farcy S, Pernelle J, Goudin N, Maillard C, Dimartino C, Deleschaux C, Dupichaud S, Lebreton C, Saunier S, Attié-Bitach T, Bahi-Buisson N, Lefort N, Thomas S
2D and 3D Human Induced Pluripotent Stem Cell-Based Models to Dissect Primary Cilium Involvement during Neocortical Development
Boutaud L et al. 2D and 3D Human Induced Pluripotent Stem Cell-Based Models to Dissect Primary Cilium Involvement during Neocortical Development. . 2022-03-25. Pubmed ID: 35389978; DOI: 10.3791/62667 IMAGINi004-AIMAGINi005-A 2022-03-25 2022-03-25 PubMed: 35389978 DOI: 10.3791/62667Associated cell lines:
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Blaszkiewicz J, Duncan SA
Advancements in Disease Modeling and Drug Discovery Using iPSC-Derived Hepatocyte-like Cells
Blaszkiewicz J et al. Advancements in Disease Modeling and Drug Discovery Using iPSC-Derived Hepatocyte-like Cells. . 2022-03-24. Pubmed ID: 35456379; DOI: 10.3390/genes13040573; PMC: PMC9030659 AKOSi002-AAKOSi003-ATRNDi031-A 2022-03-24 2022-03-24 PubMed: 35456379 DOI: 10.3390/genes13040573Associated cell lines:
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Huehnchen P, Schinke C, Bangemann N, Dordevic AD, Kern J, Maierhof SK, Hew L, Nolte L, Körtvelyessy P, Göpfert JC, Ruprecht K, Somps CJ, Blohmer JU, Sehouli J, Endres M, Boehmerle W
Neurofilament proteins as a potential biomarker in chemotherapy-induced polyneuropathy
Huehnchen P et al. Neurofilament proteins as a potential biomarker in chemotherapy-induced polyneuropathy. . 2022-03-22. Pubmed ID: 35133982; DOI: 10.1172/jci.insight.154395; PMC: PMC8986065 BIHi002-ABIHi005-ABIHi263-ABIHi264-A 2022-03-22 2022-03-22 PubMed: 35133982 DOI: 10.1172/jci.insight.154395 -
Torz L, Niss K, Lundh S, Rekling JC, Quintana CD, Frazier SED, Mercer AJ, Cornea A, Bertelsen CV, Gerstenberg MK, Hansen AMK, Guldbrandt M, Lykkesfeldt J, John LM, Villaescusa JC, Petersen N
NPFF Decreases Activity of Human Arcuate NPY Neurons: A Study in Embryonic-Stem-Cell-Derived Model
Torz L et al. NPFF Decreases Activity of Human Arcuate NPY Neurons: A Study in Embryonic-Stem-Cell-Derived Model. . 2022-03-17. Pubmed ID: 35328681; DOI: 10.3390/ijms23063260; PMC: PMC8948797 NOVOe001-A 2022-03-17 2022-03-17 PubMed: 35328681 DOI: 10.3390/ijms23063260Associated cell lines:
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Garipler G, Lu C, Morrissey A, Lopez-Zepeda LS, Pei Y, Vidal SE, Zen Petisco Fiore AP, Aydin B, Stadtfeld M, Ohler U, Mahony S, Sanjana NE, Mazzoni EO
The BTB transcription factors ZBTB11 and ZFP131 maintain pluripotency by repressing pro-differentiation genes
Garipler G et al. The BTB transcription factors ZBTB11 and ZFP131 maintain pluripotency by repressing pro-differentiation genes. . 2022-03-15. Pubmed ID: 35294876; DOI: 10.1016/j.celrep.2022.110524; PMC: PMC8972945 NYGCe001-A 2022-03-15 2022-03-15 PubMed: 35294876 DOI: 10.1016/j.celrep.2022.110524Associated cell lines:
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Vivas A, van den Berg A, Passier R, Odijk M, van der Meer AD
Fluidic circuit board with modular sensor and valves enables stand-alone, tubeless microfluidic flow control in organs-on-chips
Vivas A et al. Fluidic circuit board with modular sensor and valves enables stand-alone, tubeless microfluidic flow control in organs-on-chips. . 2022-03-15. Pubmed ID: 35178541; DOI: 10.1039/d1lc00999k; PMC: PMC8922413 ESIBIe003-A 2022-03-15 2022-03-15 PubMed: 35178541 DOI: 10.1039/d1lc00999kAssociated cell lines:
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Moczulska H, Serafin M, Wojda K, Borowiec M, Sieroszewski P
Fetal Nasal Bone Hypoplasia in the Second Trimester as a Marker of Multiple Genetic Syndromes
Moczulska H et al. Fetal Nasal Bone Hypoplasia in the Second Trimester as a Marker of Multiple Genetic Syndromes. . 2022-03-10. Pubmed ID: 35329839; DOI: 10.3390/jcm11061513; PMC: PMC8954562 GZHMCi003-A 2022-03-10 2022-03-10 PubMed: 35329839 DOI: 10.3390/jcm11061513Associated cell lines:
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Zywitza V, Rusha E, Shaposhnikov D, Ruiz-Orera J, Telugu N, Rishko V, Hayashi M, Michel G, Wittler L, Stejskal J, Holtze S, Göritz F, Hermes R, Wang J, Izsvák Z, Colleoni S, Lazzari G, Galli C, Hildebrandt TB, Hayashi K, Diecke S, Drukker M
Naïve-like pluripotency to pave the way for saving the northern white rhinoceros from extinction
Zywitza V et al. Naïve-like pluripotency to pave the way for saving the northern white rhinoceros from extinction. . 2022-03-08. Pubmed ID: 35260583; DOI: 10.1038/s41598-022-07059-w; PMC: PMC8904600 BIHi005-A 2022-03-08 2022-03-08 PubMed: 35260583 DOI: 10.1038/s41598-022-07059-wAssociated cell lines:
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Hauser S, Helm J, Kraft M, Korneck M, Hübener-Schmid J, Schöls L
Allele-specific targeting of mutant ataxin-3 by antisense oligonucleotides in SCA3-iPSC-derived neurons
Hauser S et al. Allele-specific targeting of mutant ataxin-3 by antisense oligonucleotides in SCA3-iPSC-derived neurons. . 2022-03-08. Pubmed ID: 34938609; DOI: 10.1016/j.omtn.2021.11.015; PMC: PMC8649108 HIHCNi002-A 2022-03-08 2022-03-08 PubMed: 34938609 DOI: 10.1016/j.omtn.2021.11.015Associated cell lines:
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Li L, Yi H, Liu Z, Long P, Pan T, Huang Y, Li Y, Li Q, Ma Y
Genetic correction of concurrent α- and β-thalassemia patient-derived pluripotent stem cells by the CRISPR-Cas9 technology
Li L et al. Genetic correction of concurrent α- and β-thalassemia patient-derived pluripotent stem cells by the CRISPR-Cas9 technology. . 2022-03-07. Pubmed ID: 35255977; DOI: 10.1186/s13287-022-02768-5; PMC: PMC8900422 HNMUi002-AHNMUi003-AHNMUi004-AHNMUi005-AHNMUi006-AHNMUi007-AHNMUi008-AHNMUi009-AHNMUi010-A 2022-03-07 2022-03-07 PubMed: 35255977 DOI: 10.1186/s13287-022-02768-5Associated cell lines:
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Taubenschmid-Stowers J, Rostovskaya M, Santos F, Ljung S, Argelaguet R, Krueger F, Nichols J, Reik W
8C-like cells capture the human zygotic genome activation program in vitro
Taubenschmid-Stowers J et al. 8C-like cells capture the human zygotic genome activation program in vitro. . 2022-03-03. Pubmed ID: 35216671; DOI: 10.1016/j.stem.2022.01.014; PMC: PMC8901440 WAe009-ACAMe001-A 2022-03-03 2022-03-03 PubMed: 35216671 DOI: 10.1016/j.stem.2022.01.014 -
Raines R, McKnight I, White H, Legg K, Lee C, Li W, Lee PHU, Shim JW
Drug-Targeted Genomes: Mutability of Ion Channels and GPCRs
Raines R et al. Drug-Targeted Genomes: Mutability of Ion Channels and GPCRs. . 2022-03-03. Pubmed ID: 35327396; DOI: 10.3390/biomedicines10030594; PMC: PMC8945769 UUIGPi013-A 2022-03-03 2022-03-03 PubMed: 35327396 DOI: 10.3390/biomedicines10030594Associated cell lines:
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Harvey JP, Sladen PE, Yu-Wai-Man P, Cheetham ME
Induced Pluripotent Stem Cells for Inherited Optic Neuropathies-Disease Modeling and Therapeutic Development
Harvey JP et al. Induced Pluripotent Stem Cells for Inherited Optic Neuropathies-Disease Modeling and Therapeutic Development. . 2022-03-01. Pubmed ID: 34629400; DOI: 10.1097/wno.0000000000001375 IISHDOi003-AIMBPASi001-A 2022-03-01 2022-03-01 PubMed: 34629400 DOI: 10.1097/wno.0000000000001375Associated cell lines:
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Hernández-Ainsa C, López-Gallardo E, García-Jiménez MC, Climent-Alcalá FJ, Rodríguez-Vigil C, García Fernández de Villalta M, Artuch R, Montoya J, Ruiz-Pesini E, Emperador S
Development and characterization of cell models harbouring mtDNA deletions for in vitro study of Pearson syndrome
Hernández-Ainsa C et al. Development and characterization of cell models harbouring mtDNA deletions for in vitro study of Pearson syndrome. . 2022-03-01. Pubmed ID: 35191981; DOI: 10.1242/dmm.049083; PMC: PMC8906170 FINCBi002-AFINCBi003-A 2022-03-01 2022-03-01 PubMed: 35191981 DOI: 10.1242/dmm.049083Associated cell lines:
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Hong J, Cheng YS, Yang S, Swaroop M, Xu M, Beers J, Zou J, Huang W, Marugan JJ, Cai X, Zheng W
iPS-derived neural stem cells for disease modeling and evaluation of therapeutics for mucopolysaccharidosis type II
Hong J et al. iPS-derived neural stem cells for disease modeling and evaluation of therapeutics for mucopolysaccharidosis type II. . 2022-03-01. Pubmed ID: 34990619; DOI: 10.1016/j.yexcr.2021.113007; PMC: PMC8810712 TRNDi008-A 2022-03-01 2022-03-01 PubMed: 34990619 DOI: 10.1016/j.yexcr.2021.113007Associated cell lines:
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Nguyen XP, Vilkaite A, Messmer B, Dietrich JE, Hinderhofer K, Schäkel K, Strowitzki T, Rehnitz J
Expression of FMRpolyG in Peripheral Blood Mononuclear Cells of Women with Fragile X Mental Retardation 1 Gene Premutation
Nguyen XP et al. Expression of FMRpolyG in Peripheral Blood Mononuclear Cells of Women with Fragile X Mental Retardation 1 Gene Premutation. . 2022-03-01. Pubmed ID: 35328005; DOI: 10.3390/genes13030451; PMC: PMC8951797 WAe009-AWAe009-A-16 2022-03-01 2022-03-01 PubMed: 35328005 DOI: 10.3390/genes13030451Associated cell lines:
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Cho S, Lee C, Lai C, Zhuge Y, Haddad F, Fowler M, Sallam K, Wu JC
Heterozygous LMNA mutation-carrying iPSC lines from three cardiac laminopathy patients
Cho S et al. Heterozygous LMNA mutation-carrying iPSC lines from three cardiac laminopathy patients. . 2022-03-00. Pubmed ID: 34999423; DOI: 10.1016/j.scr.2022.102657; PMC: PMC9250545 SCVIi039-ASCVIi040-ASCVIi041-A 2022-03-00 2022-03-00 PubMed: 34999423 DOI: 10.1016/j.scr.2022.102657Associated cell lines:
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Wang C, Wang Y, Xu W, Lin X, Xi J, Wang S, Lin L, Yuan F, Wang A, Wang C, Luo X, Xu Q, Yin R, Zhang Y, Huang X, Chen Y
Generation of an induced pluripotent stem cell line from an Ohtahara syndrome patient with the hemizygous mutation p.Q503Afs*28 (c.1507_1508del) in the ARX gene
Wang C et al. Generation of an induced pluripotent stem cell line from an Ohtahara syndrome patient with the hemizygous mutation p.Q503Afs*28 (c.1507_1508del) in the ARX gene. . 2022-03-00. Pubmed ID: 34968892; DOI: 10.1016/j.scr.2021.102621 SHCDNi005-A 2022-03-00 2022-03-00 PubMed: 34968892 DOI: 10.1016/j.scr.2021.102621Associated cell lines:
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Perepelina K, Khudiakov A, Rodina N, Boytsov A, Vavilova T, Zlotina A, Sokolnikova P, Kostareva A
Generation of iPSC line FAMRCi010-A from patient with restrictive cardiomyopathy carrying genetic variant FLNC p.Gly2011Arg
Perepelina K et al. Generation of iPSC line FAMRCi010-A from patient with restrictive cardiomyopathy carrying genetic variant FLNC p.Gly2011Arg. . 2022-03-00. Pubmed ID: 34971931; DOI: 10.1016/j.scr.2021.102639 FAMRCi010-A 2022-03-00 2022-03-00 PubMed: 34971931 DOI: 10.1016/j.scr.2021.102639Associated cell lines:
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Luo Y, Fernandez Vallone V, He J, Frischbutter S, Kolkhir P, Moñino-Romero S, Stachelscheid H, Streu-Haddad V, Maurer M, Siebenhaar F, Scheffel J
A novel approach for studying mast cell-driven disorders: Mast cells derived from induced pluripotent stem cells
Luo Y et al. A novel approach for studying mast cell-driven disorders: Mast cells derived from induced pluripotent stem cells. . 2022-03-00. Pubmed ID: 34371081; DOI: 10.1016/j.jaci.2021.07.027 BIHi001-ABIHi005-ABIHi001-B 2022-03-00 2022-03-00 PubMed: 34371081 DOI: 10.1016/j.jaci.2021.07.027 -
Cimarosti B, Canac R, Girardeau A, Arnaud M, Francheteau Q, Probst V, Lemarchand P, Redon R, Gourraud JB, Gaborit N, Lamirault G
Generation of human induced pluripotent stem cell lines from two patients affected by catecholamine-induced QT prolongation (CIQTP)
Cimarosti B et al. Generation of human induced pluripotent stem cell lines from two patients affected by catecholamine-induced QT prolongation (CIQTP). . 2022-03-00. Pubmed ID: 34995842; DOI: 10.1016/j.scr.2021.102649 ITXi003-AITXi004-A 2022-03-00 2022-03-00 PubMed: 34995842 DOI: 10.1016/j.scr.2021.102649 -
Rodina N, Khudiakov A, Perepelina K, Muravyev A, Boytsov A, Zlotina A, Sokolnikova P, Kostareva A
Generation of iPSC line (FAMRCi009-A) from patient with familial progressive cardiac conduction disorder carrying genetic variant FLNC p.Val2264Met
Rodina N et al. Generation of iPSC line (FAMRCi009-A) from patient with familial progressive cardiac conduction disorder carrying genetic variant FLNC p.Val2264Met. . 2022-03-00. Pubmed ID: 34971933; DOI: 10.1016/j.scr.2021.102640 FAMRCi009-A 2022-03-00 2022-03-00 PubMed: 34971933 DOI: 10.1016/j.scr.2021.102640Associated cell lines:
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Xu M, Duan X, Ren X, Liu Z, Chen S, Fang F
Generation of an iPSC line from a patient with early-onset epileptic encephalopathy carrying CARS2 (p.G476R) mutation
Xu M et al. Generation of an iPSC line from a patient with early-onset epileptic encephalopathy carrying CARS2 (p.G476R) mutation. . 2022-03-00. Pubmed ID: 34953328; DOI: 10.1016/j.scr.2021.102633 BCHCNi001-A 2022-03-00 2022-03-00 PubMed: 34953328 DOI: 10.1016/j.scr.2021.102633Associated cell lines:
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Lee C, Cho S, Lai C, Shenoy S, Vagelos R, Wu JC
Generation of three iPSC lines from dilated cardiomyopathy patients carrying a pathogenic LMNA variant
Lee C et al. Generation of three iPSC lines from dilated cardiomyopathy patients carrying a pathogenic LMNA variant. . 2022-03-00. Pubmed ID: 34954454; DOI: 10.1016/j.scr.2021.102638; PMC: PMC9436418 SCVIi020-ASCVIi021-ASCVIi022-A 2022-03-00 2022-03-00 PubMed: 34954454 DOI: 10.1016/j.scr.2021.102638Associated cell lines:
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Zakharova IS, Shevchenko AI, Tmoyan NA, Elisaphenko EA, Zubkova ES, Sleptcov AA, Nazarenko MS, Ezhov MV, Kukharchuk VV, Parfyonova YV, Zakian SM
Induced pluripotent stem cell line ICGi036-A generated by reprogramming peripheral blood mononuclear cells from a patient with familial hypercholesterolemia caused due to compound heterozygous p.Ser177Leu/p.Cys352Arg mutations in LDLR
Zakharova IS et al. Induced pluripotent stem cell line ICGi036-A generated by reprogramming peripheral blood mononuclear cells from a patient with familial hypercholesterolemia caused due to compound heterozygous p.Ser177Leu/p.Cys352Arg mutations in LDLR. . 2022-03-00. Pubmed ID: 34999421; DOI: 10.1016/j.scr.2022.102653 ICGi036-A 2022-03-00 2022-03-00 PubMed: 34999421 DOI: 10.1016/j.scr.2022.102653Associated cell lines:
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Hu Xiaofei, Chen Leilei, Zhan Chengcheng, Xu Kai, Lou Ming, Chang Keke
Thermodynamic assessment of the Fe–Ni–Rh–Ti system
Hu Xiaofei et al. Thermodynamic assessment of the Fe–Ni–Rh–Ti system. . 2022-03-00. DOI: 10.1016/j.calphad.2021.102386 ZZUNEUi003-A 2022-03-00 2022-03-00 DOI: 10.1016/j.calphad.2021.102386Associated cell lines:
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Grigor'eva EV, Drozdova ES, Sorogina DA, Malakhova AA, Pavlova SV, Vyatkin YV, Khabarova EA, Rzaev JA, Medvedev SP, Zakian SM
Generation of induced pluripotent stem cell line, ICGi034-A, by reprogramming peripheral blood mononuclear cells from a patient with Parkinson's disease associated with GBA mutation
Grigor'eva EV et al. Generation of induced pluripotent stem cell line, ICGi034-A, by reprogramming peripheral blood mononuclear cells from a patient with Parkinson's disease associated with GBA mutation. . 2022-03-00. Pubmed ID: 35007918; DOI: 10.1016/j.scr.2021.102651 ICGi034-A 2022-03-00 2022-03-00 PubMed: 35007918 DOI: 10.1016/j.scr.2021.102651Associated cell lines:
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Girardeau A, Atticus D, Canac R, Cimarosti B, Caillaud A, Chariau C, Simonet F, Cariou B, Charpentier F, Gourraud JB, Probst V, Belbachir N, Jesel L, Lemarchand P, Barc J, Redon R, Gaborit N, Lamirault G
Generation of human induced pluripotent stem cell lines from four unrelated healthy control donors carrying European genetic background
Girardeau A et al. Generation of human induced pluripotent stem cell lines from four unrelated healthy control donors carrying European genetic background. . 2022-03-00. Pubmed ID: 34999420; DOI: 10.1016/j.scr.2021.102647 ITXi005-AITXi006-AITXi007-AITXi008-A 2022-03-00 2022-03-00 PubMed: 34999420 DOI: 10.1016/j.scr.2021.102647 -
Hernández-Ainsa C, Nascimento A, Jou C, Artuch R, Montoya J, Ruiz-Pesini E, Emperador S
Generation of an induced pluripotent stem cell line from a compound heterozygous patient in TK2 gene
Hernández-Ainsa C et al. Generation of an induced pluripotent stem cell line from a compound heterozygous patient in TK2 gene. . 2022-03-00. Pubmed ID: 34973561; DOI: 10.1016/j.scr.2021.102632 UNIZARi001-A 2022-03-00 2022-03-00 PubMed: 34973561 DOI: 10.1016/j.scr.2021.102632Associated cell lines:
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Sik Jung E, Hun Kim J, Chang MY, Hong W, Quan Z, Hyun Kim S, You S, Kim DS, Jang J, Lee SH, Henry Kim H, Chul Kang H
Generation of mutation-corrected induced pluripotent stem cell lines derived from adrenoleukodystrophy patient by using homology directed repair
Sik Jung E et al. Generation of mutation-corrected induced pluripotent stem cell lines derived from adrenoleukodystrophy patient by using homology directed repair. . 2022-03-00. Pubmed ID: 35042083; DOI: 10.1016/j.scr.2022.102664 SCHi001-ASCHi001-A-1 2022-03-00 2022-03-00 PubMed: 35042083 DOI: 10.1016/j.scr.2022.102664Associated cell lines:
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Chechetkina SA, Khabarova AA, Chvileva AS, Kurchenko OM, Smirnov AV, Yunusova AM, Kotov IN, Musatova EV, Pomerantseva EA, Volovikov EA, Lagarkova MA, Shnaider TA, Pristyazhnyuk IE
Generation of two iPSC lines from healthy donor with a heterozygous mutation in the VPS13B gene
Chechetkina SA et al. Generation of two iPSC lines from healthy donor with a heterozygous mutation in the VPS13B gene. . 2022-03-00. Pubmed ID: 35026660; DOI: 10.1016/j.scr.2021.102648 ICGi035-AICGi035-B 2022-03-00 2022-03-00 PubMed: 35026660 DOI: 10.1016/j.scr.2021.102648 -
Lee OH, Lee S, Park M, Moon S, Hwang S, Kim B, Kim CY, Lee DR, Shim SH, Park KH, Chung HM, Choi Y
Generation of a B2M homozygous knockout human somatic cell nuclear transfer-derived embryonic stem cell line using the CRISPR/Cas9 system
Lee OH et al. Generation of a B2M homozygous knockout human somatic cell nuclear transfer-derived embryonic stem cell line using the CRISPR/Cas9 system. . 2022-03-00. Pubmed ID: 34971932; DOI: 10.1016/j.scr.2021.102643 CHAHESe001-ACHAHESe001-A-1 2022-03-00 2022-03-00 PubMed: 34971932 DOI: 10.1016/j.scr.2021.102643Associated cell lines:
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Qi Z, Cui Y, Shi L, Wang J, Zhao Q, Luan J, Han J
Generation of a non-integrated induced pluripotent stem cell line (SMBCi009-A) from urine-derived cells of a Chinese Familial hypercholesterolemia patient
Qi Z et al. Generation of a non-integrated induced pluripotent stem cell line (SMBCi009-A) from urine-derived cells of a Chinese Familial hypercholesterolemia patient. . 2022-03-00. Pubmed ID: 34974203; DOI: 10.1016/j.scr.2021.102624 SMBCi009-A 2022-03-00 2022-03-00 PubMed: 34974203 DOI: 10.1016/j.scr.2021.102624Associated cell lines:
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Dreßen M, Luzius T, Lahm H, Neb I, Doppler SA, Schneider S, Dzilic E, Lange R, Krane M
Establishment of an induced pluripotent stem cell line DHMi005-A from a healthy male proband
Dreßen M et al. Establishment of an induced pluripotent stem cell line DHMi005-A from a healthy male proband. . 2022-03-00. Pubmed ID: 35033855; DOI: 10.1016/j.scr.2022.102662 DHMi005-A 2022-03-00 2022-03-00 PubMed: 35033855 DOI: 10.1016/j.scr.2022.102662Associated cell lines:
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Bhattacharjee G, Gohil N, Khambhati K, Mani I, Maurya R, Karapurkar JK, Gohil J, Chu DT, Vu-Thi H, Alzahrani KJ, Show PL, Rawal RM, Ramakrishna S, Singh V
Current approaches in CRISPR-Cas9 mediated gene editing for biomedical and therapeutic applications
Bhattacharjee G et al. Current approaches in CRISPR-Cas9 mediated gene editing for biomedical and therapeutic applications. . 2022-03-00. Pubmed ID: 35149141; DOI: 10.1016/j.jconrel.2022.02.005 YCMi001-BYCMi001-B-1 2022-03-00 2022-03-00 PubMed: 35149141 DOI: 10.1016/j.jconrel.2022.02.005Associated cell lines:
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Han L, He H, Yang Y, Meng Q, Ye F, Chen G, Zhang J
Distinctive Clinical and Pathologic Features of Immature Teratomas Arising from Induced Pluripotent Stem Cell-Derived Beta Cell Injection in a Diabetes Patient
Han L et al. Distinctive Clinical and Pathologic Features of Immature Teratomas Arising from Induced Pluripotent Stem Cell-Derived Beta Cell Injection in a Diabetes Patient. . 2022-03-00. Pubmed ID: 35018826; DOI: 10.1089/scd.2021.0255 SHCDNi002-A 2022-03-00 2022-03-00 PubMed: 35018826 DOI: 10.1089/scd.2021.0255Associated cell lines:
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Li C, Cai L, Dong J, Ning S, Zhou J, Wu H, Cui Y, Qin L, Yang X
Establishment of human embryonic stem cell (SKLRMe001-A)carrying Azoospermic factor c (AZFc) deletions
Li C et al. Establishment of human embryonic stem cell (SKLRMe001-A)carrying Azoospermic factor c (AZFc) deletions. . 2022-03-00. Pubmed ID: 34952435; DOI: 10.1016/j.scr.2021.102625 SKLRMe001-A 2022-03-00 2022-03-00 PubMed: 34952435 DOI: 10.1016/j.scr.2021.102625Associated cell lines:
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Ma S, Saleem A, Li X, Lu WJ, Jiang H
Generation of a COL1A2 homozygous knockout stem cell line via CRISPR/Cas9 system
Ma S et al. Generation of a COL1A2 homozygous knockout stem cell line via CRISPR/Cas9 system. . 2022-03-00. Pubmed ID: 34999419; DOI: 10.1016/j.scr.2022.102652 WAe009-AWAe009-A-36WAe009-A-72 2022-03-00 2022-03-00 PubMed: 34999419 DOI: 10.1016/j.scr.2022.102652Associated cell lines:
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Cai H, Pang Y, Jia L
Generation of an induced pluripotent stem cell line (ICNDXHi001-A) from a patient with frontotemporal dementia carrying a heterozygous mutation c.796C > G (p.L266V) in MAPT
Cai H et al. Generation of an induced pluripotent stem cell line (ICNDXHi001-A) from a patient with frontotemporal dementia carrying a heterozygous mutation c.796C > G (p.L266V) in MAPT. . 2022-03-00. Pubmed ID: 34995843; DOI: 10.1016/j.scr.2022.102654 ICNDXHi001-A 2022-03-00 2022-03-00 PubMed: 34995843 DOI: 10.1016/j.scr.2022.102654Associated cell lines:
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Zhang W, Zhang Y, Li X, Cao Z, Mo Q, Sheng R, Ling C, Chi J, Yao Q, Chen J, Wang H
Multifunctional polyphenol-based silk hydrogel alleviates oxidative stress and enhances endogenous regeneration of osteochondral defects
Zhang W et al. Multifunctional polyphenol-based silk hydrogel alleviates oxidative stress and enhances endogenous regeneration of osteochondral defects. . 2022-03-00. Pubmed ID: 35469254; DOI: 10.1016/j.mtbio.2022.100251; PMC: PMC9034395 SDQLCHi004-A 2022-03-00 2022-03-00 PubMed: 35469254 DOI: 10.1016/j.mtbio.2022.100251Associated cell lines:
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Ngo TTT, Rossbach B, Sébastien I, Neubauer JC, Kurtz A, Hariharan K
Functional differentiation and scalable production of renal proximal tubular epithelial cells from human pluripotent stem cells in a dynamic culture system
Ngo TTT et al. Functional differentiation and scalable production of renal proximal tubular epithelial cells from human pluripotent stem cells in a dynamic culture system. . 2022-03-00. Pubmed ID: 35102634; DOI: 10.1111/cpr.13190; PMC: PMC8891564 WAe001-AWISCi004-ABCRTi005-A 2022-03-00 2022-03-00 PubMed: 35102634 DOI: 10.1111/cpr.13190Associated cell lines:
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Jair Lara-Navarro I, Rebeca Jaloma-Cruz A
Current Therapies in Hemophilia: From Plasma-Derived Factor Modalities to CRISPR/Cas Alternatives
Jair Lara-Navarro I et al. Current Therapies in Hemophilia: From Plasma-Derived Factor Modalities to CRISPR/Cas Alternatives. . 2022-03-00. Pubmed ID: 35314527; DOI: 10.1620/tjem.256.197 YCMi001-BYCMi001-B-1 2022-03-00 2022-03-00 PubMed: 35314527 DOI: 10.1620/tjem.256.197Associated cell lines:
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Khampang S, Laowtammathron C, Lorthongpanich C, Klaihmon P, Chingsuwanrote P, Choavaratana R, Phornwilardsiri S, Sitthirit K, Srisook P, U-Pratya Y, Issaragrisil S
Derivation of the MUSIe002-A human embryonic stem cell line
Khampang S et al. Derivation of the MUSIe002-A human embryonic stem cell line. . 2022-03-00. Pubmed ID: 35033856; DOI: 10.1016/j.scr.2022.102660 MUSIe001-AMUSIe002-A 2022-03-00 2022-03-00 PubMed: 35033856 DOI: 10.1016/j.scr.2022.102660Associated cell lines:
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Li S, Wang Y, Sun H, Wang Z, Zhang Q, Wang Y, Yang J, Shi C, Yuan Y, Wang H, Wang A, Hu Z, Li Z, Xu Y
Establishment of induced pluripotent stem cell line (ZZUi033-A) of a male with a novel L1CAM missense mutation
Li S et al. Establishment of induced pluripotent stem cell line (ZZUi033-A) of a male with a novel L1CAM missense mutation. . 2022-03-00. Pubmed ID: 35042084; DOI: 10.1016/j.scr.2022.102663 ZZUi033-AZZUi037-A 2022-03-00 2022-03-00 PubMed: 35042084 DOI: 10.1016/j.scr.2022.102663 -
Iannello G, Patel A, Sirabella D, Corneo B, Thaker VV
Derivation and characterization of the induced pluripotent stem cell line CUIMCi004-A from a patient with a novel frameshift variant in exon 18a of OCRL
Iannello G et al. Derivation and characterization of the induced pluripotent stem cell line CUIMCi004-A from a patient with a novel frameshift variant in exon 18a of OCRL. . 2022-03-00. Pubmed ID: 35074682; DOI: 10.1016/j.scr.2021.102635; PMC: PMC9970692 CUIMCi003-ACUIMCi004-A 2022-03-00 2022-03-00 PubMed: 35074682 DOI: 10.1016/j.scr.2021.102635Associated cell lines:
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Bonilla-Pons SÀ, Nakagawa S, Bahima EG, Fernández-Blanco Á, Pesaresi M, D'Antin JC, Sebastian-Perez R, Greco D, Domínguez-Sala E, Gómez-Riera R, Compte RIB, Dierssen M, Pulido NM, Cosma MP
Müller glia fused with adult stem cells undergo neural differentiation in human retinal models
Bonilla-Pons SÀ et al. Müller glia fused with adult stem cells undergo neural differentiation in human retinal models. . 2022-03-00. Pubmed ID: 35278743; DOI: 10.1016/j.ebiom.2022.103914; PMC: PMC8917309 ESe014-A 2022-03-00 2022-03-00 PubMed: 35278743 DOI: 10.1016/j.ebiom.2022.103914Associated cell lines:
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Zhang Y, Lin Y, Zhang Y, Wang Y, Li Z, Zhu Y, Liu H, Ju W, Cui C, Chen M
Familial atrial myopathy in a large multigenerational heart-hand syndrome pedigree carrying an LMNA missense variant in rod 2B domain (p.R335W)
Zhang Y et al. Familial atrial myopathy in a large multigenerational heart-hand syndrome pedigree carrying an LMNA missense variant in rod 2B domain (p.R335W). . 2022-03-00. Pubmed ID: 34808346; DOI: 10.1016/j.hrthm.2021.11.022 JSPHi001-A 2022-03-00 2022-03-00 PubMed: 34808346 DOI: 10.1016/j.hrthm.2021.11.022Associated cell lines:
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Hong J, Xing J, Li P, Liu M, Zhu J, Li L, Li X, Dong J
Generation of a human iPSC line ZZUNEUi014-A from a patient with antithrombin deficiency caused by mutation in SERPINC1 gene
Hong J et al. Generation of a human iPSC line ZZUNEUi014-A from a patient with antithrombin deficiency caused by mutation in SERPINC1 gene. . 2022-03-00. Pubmed ID: 34973562; DOI: 10.1016/j.scr.2021.102646 ZZUNEUi014-AZZUNEUi020-A 2022-03-00 2022-03-00 PubMed: 34973562 DOI: 10.1016/j.scr.2021.102646Associated cell lines:
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Zhao Y, Cui Y, Luan J, Wang J, Shi L, Han Z, Han J
Development and identification of a induced pluripotent stem cells line (SMBCi013-A) derived from urine cells of a patient with Wilson's disease
Zhao Y et al. Development and identification of a induced pluripotent stem cells line (SMBCi013-A) derived from urine cells of a patient with Wilson's disease. . 2022-03-00. Pubmed ID: 34995846; DOI: 10.1016/j.scr.2021.102650 SMBCi013-A 2022-03-00 2022-03-00 PubMed: 34995846 DOI: 10.1016/j.scr.2021.102650Associated cell lines:
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Zhang S, Guo T, Song Y, Jiang M, Jiang Y, Dong T, Zhang S, Wang H, Hou X
Generation of a homozygous S100A1 knockout human embryonic stem cell line (WAe009-A-73) by the CRISPR/Cas9 editing system
Zhang S et al. Generation of a homozygous S100A1 knockout human embryonic stem cell line (WAe009-A-73) by the CRISPR/Cas9 editing system. . 2022-03-00. Pubmed ID: 34953326; DOI: 10.1016/j.scr.2021.102631 WAe009-AWAe009-A-73 2022-03-00 2022-03-00 PubMed: 34953326 DOI: 10.1016/j.scr.2021.102631Associated cell lines:
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Tan F, Ding C, Sun X, Wang Y, Peng Y, Liang Y, Chen Z, Tang S, Chen J
Establishment of a human induced pluripotent stem cell line (CSUASOi008-A) from a type 2 diabetic patient with retinopathy
Tan F et al. Establishment of a human induced pluripotent stem cell line (CSUASOi008-A) from a type 2 diabetic patient with retinopathy. . 2022-03-00. Pubmed ID: 34959203; DOI: 10.1016/j.scr.2021.102637 CSUASOi008-A 2022-03-00 2022-03-00 PubMed: 34959203 DOI: 10.1016/j.scr.2021.102637Associated cell lines:
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Madencioglu DA, Kruth K, Shin M, Andreasen N, Wassink T, Williams A
Generation of a human induced pluripotent stem cell line from a patient diagnosed with schizophrenia carrying a 16p11.2 deletion
Madencioglu DA et al. Generation of a human induced pluripotent stem cell line from a patient diagnosed with schizophrenia carrying a 16p11.2 deletion. . 2022-03-00. Pubmed ID: 34953327; DOI: 10.1016/j.scr.2021.102636; PMC: PMC9209596 UIi001-A 2022-03-00 2022-03-00 PubMed: 34953327 DOI: 10.1016/j.scr.2021.102636Associated cell lines:
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Ji X, Gao Y, Zhang P, Jin Z, Zhang Y, Yang M, Zhang X, Chen Q
Generation of a human iPSC line CIPi001-A from a benign familial infantile epilepsy patient related 16p11.2 deletion
Ji X et al. Generation of a human iPSC line CIPi001-A from a benign familial infantile epilepsy patient related 16p11.2 deletion. . 2022-03-00. Pubmed ID: 34995844; DOI: 10.1016/j.scr.2021.102634 CIPi001-A 2022-03-00 2022-03-00 PubMed: 34995844 DOI: 10.1016/j.scr.2021.102634Associated cell lines:
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Zou X, Wu S, Zhu T, Sun Z, Wei X, Li W, Sui R
Generation of a human induced pluripotent stem cell line (PUMCHi018-A) from an early-onset severe retinal dystrophy patient with RDH12 mutations
Zou X et al. Generation of a human induced pluripotent stem cell line (PUMCHi018-A) from an early-onset severe retinal dystrophy patient with RDH12 mutations. . 2022-03-00. Pubmed ID: 35016144; DOI: 10.1016/j.scr.2022.102655 PUMCHi018-A 2022-03-00 2022-03-00 PubMed: 35016144 DOI: 10.1016/j.scr.2022.102655Associated cell lines:
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Han X, Wu S, Sun Z, Zhu T, Wei X, Zou X, Sui R
Generation of a human induced pluripotent stem cell line PUMCHi017-A from a Choroideremia patient with CHM mutation
Han X et al. Generation of a human induced pluripotent stem cell line PUMCHi017-A from a Choroideremia patient with CHM mutation. . 2022-03-00. Pubmed ID: 35032821; DOI: 10.1016/j.scr.2022.102661 PUMCHi017-A 2022-03-00 2022-03-00 PubMed: 35032821 DOI: 10.1016/j.scr.2022.102661Associated cell lines:
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Chen F, Wang T, Yang Y, Huang Z, Dong Y, Zhang R, Chen J, Zhou Q
Generation of an induced pluripotent stem cell line (SYSUSCi001-A) from a congenital cataract patient carrying heterozygous mutations in BFSP1 and RHO
Chen F et al. Generation of an induced pluripotent stem cell line (SYSUSCi001-A) from a congenital cataract patient carrying heterozygous mutations in BFSP1 and RHO. . 2022-03-00. Pubmed ID: 34995847; DOI: 10.1016/j.scr.2021.102644 SYSUSCi001-A 2022-03-00 2022-03-00 PubMed: 34995847 DOI: 10.1016/j.scr.2021.102644Associated cell lines:
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Deng J, Li M, Li Z, Meng F, Gao J, Li J, Wang Y, Zhang L, Tang P
Establishment and characterization of an induced pluripotent stem cell line CPGHi004-A from peripheral blood mononuclear cells of a healthy adult
Deng J et al. Establishment and characterization of an induced pluripotent stem cell line CPGHi004-A from peripheral blood mononuclear cells of a healthy adult. . 2022-03-00. Pubmed ID: 34995845; DOI: 10.1016/j.scr.2022.102656 CPGHi004-A 2022-03-00 2022-03-00 PubMed: 34995845 DOI: 10.1016/j.scr.2022.102656Associated cell lines:
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Lee SH, Oh J, Lee ST, Won D, Kim S, Choi HK, Kim SJ, Han H, Yoon M, Choi JR, Yoon HG, Park SW, Kang SM, Lee SH
Generation of a human induced pluripotent stem cell line YCMi004-A from a patient with dilated cardiomyopathy carrying a protein-truncating mutation of the Titin gene and its differentiation towards cardiomyocytes
Lee SH et al. Generation of a human induced pluripotent stem cell line YCMi004-A from a patient with dilated cardiomyopathy carrying a protein-truncating mutation of the Titin gene and its differentiation towards cardiomyocytes. . 2022-03-00. Pubmed ID: 34952434; DOI: 10.1016/j.scr.2021.102629 YCMi004-A 2022-03-00 2022-03-00 PubMed: 34952434 DOI: 10.1016/j.scr.2021.102629Associated cell lines:
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Iafusco D, Zanfardino A, Piscopo A, Curto S, Troncone A, Chianese A, Rollato AS, Testa V, Iafusco F, Maione G, Pennarella A, Boccabella L, Ozen G, Palma PL, Mazzaccara C, Tinto N, Miraglia Del Giudice E
Metabolic Treatment of Wolfram Syndrome
Iafusco D et al. Metabolic Treatment of Wolfram Syndrome. . 2022-02-27. Pubmed ID: 35270448; DOI: 10.3390/ijerph19052755; PMC: PMC8910219 UNINAi001-AUNINAi002-A 2022-02-27 2022-02-27 PubMed: 35270448 DOI: 10.3390/ijerph19052755Associated cell lines:
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Davies AK, Alecu JE, Ziegler M, Vasilopoulou CG, Merciai F, Jumo H, Afshar-Saber W, Sahin M, Ebrahimi-Fakhari D, Borner GHH
AP-4-mediated axonal transport controls endocannabinoid production in neurons
Davies AK et al. AP-4-mediated axonal transport controls endocannabinoid production in neurons. . 2022-02-25. Pubmed ID: 35217685; DOI: 10.1038/s41467-022-28609-w; PMC: PMC8881493 BCHNEUi001-ABCHNEUi003-ABCHNEUi005-A 2022-02-25 2022-02-25 PubMed: 35217685 DOI: 10.1038/s41467-022-28609-wAssociated cell lines:
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Chen Carol X.-Q., You Zhipeng, Abdian Narges, Sirois Julien, Shlaifer Irina, Tabatabaei Mahdieh, Boivin Marie-Noëlle, Gaborieau Lydiane, Karamchandani Jason, Beitel Lenore K., Fon Edward A., Durcan Thomas M.
Generation of PRKN and PINK1-KO and double KO cell lines from healthy induced pluripotent stem cells using CRISPR/Cas9 editing
Chen Carol X.-Q. et al. Generation of PRKN and PINK1-KO and double KO cell lines from healthy induced pluripotent stem cells using CRISPR/Cas9 editing. . 2022-02-25. DOI: 10.1101/2022.02.25.482014 CBIGi001-ACBIGi001-A-1CBIGi001-A-2CBIGi001-A-3 2022-02-25 2022-02-25 DOI: 10.1101/2022.02.25.482014Associated cell lines:
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Uhrig M, Ezquer F, Ezquer M
Improving Cell Recovery: Freezing and Thawing Optimization of Induced Pluripotent Stem Cells
Uhrig M et al. Improving Cell Recovery: Freezing and Thawing Optimization of Induced Pluripotent Stem Cells. . 2022-02-24. Pubmed ID: 35269421; DOI: 10.3390/cells11050799; PMC: PMC8909336 XWHNi001-A 2022-02-24 2022-02-24 PubMed: 35269421 DOI: 10.3390/cells11050799Associated cell lines:
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Prokhorova D, Zhukova Eschenko N, Lemza A, Sergeeva M, Amirkhanov R, Stepanov G
Application of the CRISPR/Cas9 System to Study Regulation Pathways of the Cellular Immune Response to Influenza Virus
Prokhorova D et al. Application of the CRISPR/Cas9 System to Study Regulation Pathways of the Cellular Immune Response to Influenza Virus. . 2022-02-21. Pubmed ID: 35216030; DOI: 10.3390/v14020437; PMC: PMC8879999 KSCBi005-AKSCBi005-A-5 2022-02-21 2022-02-21 PubMed: 35216030 DOI: 10.3390/v14020437Associated cell lines:
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Yu C, Liu Q, Wang J
A physical mechanism of heterogeneity and micro-metastasis in stem cells, cancer cells, and cancer stem cells
Yu C et al. A physical mechanism of heterogeneity and micro-metastasis in stem cells, cancer cells, and cancer stem cells. . 2022-02-21. Pubmed ID: 35183090; DOI: 10.1063/5.0078196 NCCSi004-A 2022-02-21 2022-02-21 PubMed: 35183090 DOI: 10.1063/5.0078196Associated cell lines:
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Morera Cristina, Kim Jihee, Paredes-Redondo Amaia, Nobles Muriel, Rybin Denis, Moccia Robert, Kowala Anna, Meng Jinhong, Garren Seth, Liu Pentao, Morgan Jennifer E, Muntoni Francesco, Christoforou Nicolas, Owens Jane, Tinker Andrew, Lin Yung-Yao
CRISPR-mediated correction of skeletal muscle Ca2+handling in a novel DMD patient-derived pluripotent stem cell model
Morera Cristina et al. CRISPR-mediated correction of skeletal muscle Ca2+handling in a novel DMD patient-derived pluripotent stem cell model. . 2022-02-18. DOI: 10.1101/2022.02.17.480850 BIONi010-C 2022-02-18 2022-02-18 DOI: 10.1101/2022.02.17.480850Associated cell lines:
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Li W, Luo X, Poetsch MS, Oertel R, Nichani K, Schneider M, Strano A, Hasse M, Steiner RP, Cyganek L, Hettwer K, Uhlig S, Simon K, Guan K, Schubert M
Synergistic Adverse Effects of Azithromycin and Hydroxychloroquine on Human Cardiomyocytes at a Clinically Relevant Treatment Duration
Li W et al. Synergistic Adverse Effects of Azithromycin and Hydroxychloroquine on Human Cardiomyocytes at a Clinically Relevant Treatment Duration. . 2022-02-12. Pubmed ID: 35215332; DOI: 10.3390/ph15020220; PMC: PMC8877825 UMGi001-AUMGi005-AUMGi014-CUMGi020-B 2022-02-12 2022-02-12 PubMed: 35215332 DOI: 10.3390/ph15020220 -
Shiraki N, Maruyama K, Hayashi R, Oguchi A, Murakawa Y, Katayama T, Takigawa T, Sakimoto S, Quantock AJ, Tsujikawa M, Nishida K
PAX6-positive microglia evolve locally in hiPSC-derived ocular organoids
Shiraki N et al. PAX6-positive microglia evolve locally in hiPSC-derived ocular organoids. . 2022-02-08. Pubmed ID: 35030319; DOI: 10.1016/j.stemcr.2021.12.009; PMC: PMC8828554 KUIMSe001-AKUIFMSi004-C 2022-02-08 2022-02-08 PubMed: 35030319 DOI: 10.1016/j.stemcr.2021.12.009Associated cell lines:
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Krasemann S, Haferkamp U, Pfefferle S, Woo MS, Heinrich F, Schweizer M, Appelt-Menzel A, Cubukova A, Barenberg J, Leu J, Hartmann K, Thies E, Littau JL, Sepulveda-Falla D, Zhang L, Ton K, Liang Y, Matschke J, Ricklefs F, Sauvigny T, Sperhake J, Fitzek A, Gerhartl A, Brachner A, Geiger N, König EM, Bodem J, Franzenburg S, Franke A, Moese S, Müller FJ, Geisslinger G, Claussen C, Kannt A, Zaliani A, Gribbon P, Ondruschka B, Neuhaus W, Friese MA, Glatzel M, Pless O
The blood-brain barrier is dysregulated in COVID-19 and serves as a CNS entry route for SARS-CoV-2
Krasemann S et al. The blood-brain barrier is dysregulated in COVID-19 and serves as a CNS entry route for SARS-CoV-2. . 2022-02-08. Pubmed ID: 35063125; DOI: 10.1016/j.stemcr.2021.12.011; PMC: PMC8772030 WISCi004-BZIPi013-BZIPi013-E 2022-02-08 2022-02-08 PubMed: 35063125 DOI: 10.1016/j.stemcr.2021.12.011Associated cell lines:
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Stronati E, Giraldez S, Huang L, Abraham E, McGuire GR, Hsu HT, Jones KA, Estarás C
YAP1 regulates the self-organized fate patterning of hESC-derived gastruloids
Stronati E et al. YAP1 regulates the self-organized fate patterning of hESC-derived gastruloids. . 2022-02-08. Pubmed ID: 35063126; DOI: 10.1016/j.stemcr.2021.12.012; PMC: PMC8828531 WAe001-A 2022-02-08 2022-02-08 PubMed: 35063126 DOI: 10.1016/j.stemcr.2021.12.012Associated cell lines:
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Lach MS, Rosochowicz MA, Richter M, Jagiełło I, Suchorska WM, Trzeciak T
The Induced Pluripotent Stem Cells in Articular Cartilage Regeneration and Disease Modelling: Are We Ready for Their Clinical Use?
Lach MS et al. The Induced Pluripotent Stem Cells in Articular Cartilage Regeneration and Disease Modelling: Are We Ready for Their Clinical Use?. . 2022-02-03. Pubmed ID: 35159338; DOI: 10.3390/cells11030529; PMC: PMC8834349 IGIBi007-A 2022-02-03 2022-02-03 PubMed: 35159338 DOI: 10.3390/cells11030529Associated cell lines:
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Parichha A, Suresh V, Chatterjee M, Kshirsagar A, Ben-Reuven L, Olender T, Taketo MM, Radosevic V, Bobic-Rasonja M, Trnski S, Holtzman MJ, Jovanov-Milosevic N, Reiner O, Tole S
Constitutive activation of canonical Wnt signaling disrupts choroid plexus epithelial fate
Parichha A et al. Constitutive activation of canonical Wnt signaling disrupts choroid plexus epithelial fate. . 2022-02-02. Pubmed ID: 35110543; DOI: 10.1038/s41467-021-27602-z; PMC: PMC8810795 WIBRe001-A 2022-02-02 2022-02-02 PubMed: 35110543 DOI: 10.1038/s41467-021-27602-zAssociated cell lines:
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Malik MNH, Waqas SF, Zeitvogel J, Cheng J, Geffers R, Gouda ZA, Elsaman AM, Radwan AR, Schefzyk M, Braubach P, Auber B, Olmer R, Müsken M, Roesner LM, Gerold G, Schuchardt S, Merkert S, Martin U, Meissner F, Werfel T, Pessler F
Congenital deficiency reveals critical role of ISG15 in skin homeostasis
Malik MNH et al. Congenital deficiency reveals critical role of ISG15 in skin homeostasis. . 2022-02-01. Pubmed ID: 34847081; DOI: 10.1172/jci141573; PMC: PMC8803340 MHHi001-A 2022-02-01 2022-02-01 PubMed: 34847081 DOI: 10.1172/jci141573Associated cell lines:
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Kumari D, Fisher EA, Brodsky JL
Hsp40s play distinct roles during the initial stages of apolipoprotein B biogenesis
Kumari D et al. Hsp40s play distinct roles during the initial stages of apolipoprotein B biogenesis. . 2022-02-01. Pubmed ID: 34910568; DOI: 10.1091/mbc.e21-09-0436; PMC: PMC9236142 LIBUCi001-ALIBUCi002-AJMUi001-AJMUi001-A-1 2022-02-01 2022-02-01 PubMed: 34910568 DOI: 10.1091/mbc.e21-09-0436Associated cell lines:
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Hosseini Shabanan S, Seyedmirzaei H, Barnea A, Hanaei S, Rezaei N
Stem cell transplantation as a progressing treatment for retinitis pigmentosa
Hosseini Shabanan S et al. Stem cell transplantation as a progressing treatment for retinitis pigmentosa. . 2022-02-00. Pubmed ID: 35001210; DOI: 10.1007/s00441-021-03551-3 INMi001-AFRIMOi001-AFRIMOi002-AFRIMOi005-ANUIGi027-ANUIGi028-ANUIGi029-AZOCi001-ACSUASOi003-AUCLi014-AUCLi015-A 2022-02-00 2022-02-00 PubMed: 35001210 DOI: 10.1007/s00441-021-03551-3Associated cell lines:
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Zhao H, Li S, He L, Tang F, Han X, Deng W, Lin Z, Huang R, Li Z
Ameliorating Effect of Umbilical Cord Mesenchymal Stem Cells in a Human Induced Pluripotent Stem Cell Model of Dravet Syndrome
Zhao H et al. Ameliorating Effect of Umbilical Cord Mesenchymal Stem Cells in a Human Induced Pluripotent Stem Cell Model of Dravet Syndrome. . 2022-02-00. Pubmed ID: 34766239; DOI: 10.1007/s12035-021-02633-1 USTCi001-A 2022-02-00 2022-02-00 PubMed: 34766239 DOI: 10.1007/s12035-021-02633-1Associated cell lines:
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Stenzig J, Lemoine MD, Stoter AMS, Wrona KM, Lemme M, Mulla W, Etzion Y, Eschenhagen T, Hirt MN
Recapitulation of dyssynchrony-associated contractile impairment in asymmetrically paced engineered heart tissue
Stenzig J et al. Recapitulation of dyssynchrony-associated contractile impairment in asymmetrically paced engineered heart tissue. . 2022-02-00. Pubmed ID: 34634355; DOI: 10.1016/j.yjmcc.2021.10.001; PMC: PMC8828044 UKEi003-C 2022-02-00 2022-02-00 PubMed: 34634355 DOI: 10.1016/j.yjmcc.2021.10.001Associated cell lines:
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Hommersom MP, Buijsen RAM, van Roon-Mom WMC, van de Warrenburg BPC, van Bokhoven H
Human Induced Pluripotent Stem Cell-Based Modelling of Spinocerebellar Ataxias
Hommersom MP et al. Human Induced Pluripotent Stem Cell-Based Modelling of Spinocerebellar Ataxias. . 2022-02-00. Pubmed ID: 34031815; DOI: 10.1007/s12015-021-10184-0; PMC: PMC8930896 ZZUi004-ALUMCi002-ALUMCi003-AMUSIi004-AHIHCNi002-AZZUNEUi002-ACSUXHi001-AIGIBi002-AIGIBi003-AIGIBi004-A 2022-02-00 2022-02-00 PubMed: 34031815 DOI: 10.1007/s12015-021-10184-0Associated cell lines:
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Ren X, Lei W, Huang S, Shi D, Li X
Rapamycin Treatment Is Beneficial for the Generation of Rabbit-Induced Pluripotent Stem-Like Cells
Ren X et al. Rapamycin Treatment Is Beneficial for the Generation of Rabbit-Induced Pluripotent Stem-Like Cells. . 2022-02-00. Pubmed ID: 35085453; DOI: 10.1089/cell.2021.0128 IGIBi001-A 2022-02-00 2022-02-00 PubMed: 35085453 DOI: 10.1089/cell.2021.0128Associated cell lines:
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Ackermann M, Rafiei Hashtchin A, Manstein F, Carvalho Oliveira M, Kempf H, Zweigerdt R, Lachmann N
Continuous human iPSC-macrophage mass production by suspension culture in stirred tank bioreactors
Ackermann M et al. Continuous human iPSC-macrophage mass production by suspension culture in stirred tank bioreactors. . 2022-02-00. Pubmed ID: 35039668; DOI: 10.1038/s41596-021-00654-7; PMC: PMC7612500 MHHi015-AMHHi015-B 2022-02-00 2022-02-00 PubMed: 35039668 DOI: 10.1038/s41596-021-00654-7 -
Huang D, Heath Jeffery RC, Aung-Htut MT, McLenachan S, Fletcher S, Wilton SD, Chen FK
Stargardt disease and progress in therapeutic strategies
Huang D et al. Stargardt disease and progress in therapeutic strategies. . 2022-02-00. Pubmed ID: 34455905; DOI: 10.1080/13816810.2021.1966053 FRIMOi003-AFRIMOi004-A 2022-02-00 2022-02-00 PubMed: 34455905 DOI: 10.1080/13816810.2021.1966053Associated cell lines:
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Kumawat V, Tripathi PP, Patidar GK
Therapeutic apheresis and non-blood donor related apheresis current practices at various blood centres of healthcare organisations of India: A brief online survey
Kumawat V et al. Therapeutic apheresis and non-blood donor related apheresis current practices at various blood centres of healthcare organisations of India: A brief online survey. . 2022-02-00. Pubmed ID: 34825419; DOI: 10.1111/tme.12837 NCCSi003-A 2022-02-00 2022-02-00 PubMed: 34825419 DOI: 10.1111/tme.12837Associated cell lines:
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Moreira A, Müller M, Costa PF, Kohl Y
Advanced In Vitro Lung Models for Drug and Toxicity Screening: The Promising Role of Induced Pluripotent Stem Cells
Moreira A et al. Advanced In Vitro Lung Models for Drug and Toxicity Screening: The Promising Role of Induced Pluripotent Stem Cells. . 2022-02-00. Pubmed ID: 34962104; DOI: 10.1002/adbi.202101139 MHHi018-A 2022-02-00 2022-02-00 PubMed: 34962104 DOI: 10.1002/adbi.202101139Associated cell lines:
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Chidipi B, Angulo MB, Shah SI, Rieser M, Ullah G, McDonald TV, Noujaim SF
The dynamin-related protein 1 is decreased and the mitochondrial network is altered in Friedreich's ataxia cardiomyopathy
Chidipi B et al. The dynamin-related protein 1 is decreased and the mitochondrial network is altered in Friedreich's ataxia cardiomyopathy. . 2022-02-00. Pubmed ID: 34923139; DOI: 10.1016/j.biocel.2021.106137; PMC: PMC8820922 USFi001-A 2022-02-00 2022-02-00 PubMed: 34923139 DOI: 10.1016/j.biocel.2021.106137Associated cell lines:
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Sampathkumar NK, Sundaram VK, Danthi PS, Barakat R, Solomon S, Mondal M, Carre I, El Jalkh T, Padilla-Ferrer A, Grenier J, Massaad C, Mitchell JC
RNA-Seq is not required to determine stable reference genes for qPCR normalization
Sampathkumar NK et al. RNA-Seq is not required to determine stable reference genes for qPCR normalization. . 2022-02-00. Pubmed ID: 35226660; DOI: 10.1371/journal.pcbi.1009868; PMC: PMC8912902 BIONi010-CBIONi010-C-17 2022-02-00 2022-02-00 PubMed: 35226660 DOI: 10.1371/journal.pcbi.1009868Associated cell lines:
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Yang NJ, Isensee J, Neel DV, Quadros AU, Zhang HB, Lauzadis J, Liu SM, Shiers S, Belu A, Palan S, Marlin S, Maignel J, Kennedy-Curran A, Tong VS, Moayeri M, Röderer P, Nitzsche A, Lu M, Pentelute BL, Brüstle O, Tripathi V, Foster KA, Price TJ, Collier RJ, Leppla SH, Puopolo M, Bean BP, Cunha TM, Hucho T, Chiu IM
Anthrax toxins regulate pain signaling and can deliver molecular cargoes into ANTXR2(+) DRG sensory neurons
Yang NJ et al. Anthrax toxins regulate pain signaling and can deliver molecular cargoes into ANTXR2(+) DRG sensory neurons. . 2022-02-00. Pubmed ID: 34931070; DOI: 10.1038/s41593-021-00973-8; PMC: PMC9388775 UKBi013-A 2022-02-00 2022-02-00 PubMed: 34931070 DOI: 10.1038/s41593-021-00973-8Associated cell lines:
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Del Campo CV, Liaw NY, Gunadasa-Rohling M, Matthaei M, Braga L, Kennedy T, Salinas G, Voigt N, Giacca M, Zimmermann WH, Riley PR
Regenerative potential of epicardium-derived extracellular vesicles mediated by conserved miRNA transfer
Del Campo CV et al. Regenerative potential of epicardium-derived extracellular vesicles mediated by conserved miRNA transfer. . 2022-01-29. Pubmed ID: 33599250; DOI: 10.1093/cvr/cvab054; PMC: PMC8803084 WAe009-A 2022-01-29 2022-01-29 PubMed: 33599250 DOI: 10.1093/cvr/cvab054Associated cell lines:
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Bull D, Schweitzer C, Bichsel C, Britschgi M, Gutbier S
Generation of an hiPSC-Derived Co-Culture System to Assess the Effects of Neuroinflammation on Blood-Brain Barrier Integrity
Bull D et al. Generation of an hiPSC-Derived Co-Culture System to Assess the Effects of Neuroinflammation on Blood-Brain Barrier Integrity. . 2022-01-26. Pubmed ID: 35159229; DOI: 10.3390/cells11030419; PMC: PMC8834542 BIONi010-C 2022-01-26 2022-01-26 PubMed: 35159229 DOI: 10.3390/cells11030419Associated cell lines:
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Morais MRPT, Tian P, Lawless C, Murtuza-Baker S, Hopkinson L, Woods S, Mironov A, Long DA, Gale DP, Zorn TMT, Kimber SJ, Zent R, Lennon R
Kidney organoids recapitulate human basement membrane assembly in health and disease
Morais MRPT et al. Kidney organoids recapitulate human basement membrane assembly in health and disease. . 2022-01-25. Pubmed ID: 35076391; DOI: 10.7554/elife.73486; PMC: PMC8849328 WTSIi503-AWTSIi519-AWTSIi623-A 2022-01-25 2022-01-25 PubMed: 35076391 DOI: 10.7554/elife.73486Associated cell lines:
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Koncz I, Verkerk AO, Nicastro M, Wilders R, Árpádffy-Lovas T, Magyar T, Tóth N, Nagy N, Madrid M, Lin Z, Efimov IR
Acetylcholine Reduces I(Kr) and Prolongs Action Potentials in Human Ventricular Cardiomyocytes
Koncz I et al. Acetylcholine Reduces I(Kr) and Prolongs Action Potentials in Human Ventricular Cardiomyocytes. . 2022-01-24. Pubmed ID: 35203454; DOI: 10.3390/biomedicines10020244; PMC: PMC8869322 LUMCi004-A 2022-01-24 2022-01-24 PubMed: 35203454 DOI: 10.3390/biomedicines10020244Associated cell lines:
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Meier AB, Raj Murthi S, Rawat H, Toepfer CN, Santamaria G, Schmid M, Mastantuono E, Schwarzmayr T, Berutti R, Cleuziou J, Ewert P, Görlach A, Klingel K, Laugwitz KL, Seidman CE, Seidman JG, Moretti A, Wolf CM
Cell cycle defects underlie childhood-onset cardiomyopathy associated with Noonan syndrome
Meier AB et al. Cell cycle defects underlie childhood-onset cardiomyopathy associated with Noonan syndrome. . 2022-01-21. Pubmed ID: 34988410; DOI: 10.1016/j.isci.2021.103596; PMC: PMC8704485 MRIi001-AMRIi003-AMRIi025-A 2022-01-21 2022-01-21 PubMed: 34988410 DOI: 10.1016/j.isci.2021.103596 -
Mandal G, Moráň L, Pečinka L, Vaňhara P, Havel J
Matrix enrichment by black phosphorus improves ionization and reproducibility of mass spectrometry of intact cells, peptides, and amino acids
Mandal G et al. Matrix enrichment by black phosphorus improves ionization and reproducibility of mass spectrometry of intact cells, peptides, and amino acids. . 2022-01-21. Pubmed ID: 35064192; DOI: 10.1038/s41598-022-05197-9; PMC: PMC8782824 MUNIe007-A 2022-01-21 2022-01-21 PubMed: 35064192 DOI: 10.1038/s41598-022-05197-9Associated cell lines:
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Manos JD, Preiss CN, Venkat N, Tamm J, Reinhardt P, Kwon T, Wu J, Winter AD, Jahn TR, Yanamandra K, Titterton K, Karran E, Langlois X
Uncovering specificity of endogenous TAU aggregation in a human iPSC-neuron TAU seeding model
Manos JD et al. Uncovering specificity of endogenous TAU aggregation in a human iPSC-neuron TAU seeding model. . 2022-01-21. Pubmed ID: 35072001; DOI: 10.1016/j.isci.2021.103658; PMC: PMC8761709 BIONi010-CBIONi010-C-13 2022-01-21 2022-01-21 PubMed: 35072001 DOI: 10.1016/j.isci.2021.103658Associated cell lines:
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Cakir B, Tanaka Y, Kiral FR, Xiang Y, Dagliyan O, Wang J, Lee M, Greaney AM, Yang WS, duBoulay C, Kural MH, Patterson B, Zhong M, Kim J, Bai Y, Min W, Niklason LE, Patra P, Park IH
Expression of the transcription factor PU.1 induces the generation of microglia-like cells in human cortical organoids
Cakir B et al. Expression of the transcription factor PU.1 induces the generation of microglia-like cells in human cortical organoids. . 2022-01-20. Pubmed ID: 35058453; DOI: 10.1038/s41467-022-28043-y; PMC: PMC8776770 KMUe003-A 2022-01-20 2022-01-20 PubMed: 35058453 DOI: 10.1038/s41467-022-28043-yAssociated cell lines:
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Park HJ, Han A, Kim JY, Choi J, Bae HS, Cho GB, Shin H, Shin EJ, Lee KI, Kim S, Lee JY, Song J
SUPT4H1-edited stem cell therapy rescues neuronal dysfunction in a mouse model for Huntington's disease
Park HJ et al. SUPT4H1-edited stem cell therapy rescues neuronal dysfunction in a mouse model for Huntington's disease. . 2022-01-19. Pubmed ID: 35046408; DOI: 10.1038/s41536-021-00198-0; PMC: PMC8770473 CHAi001-A 2022-01-19 2022-01-19 PubMed: 35046408 DOI: 10.1038/s41536-021-00198-0Associated cell lines:
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David C, Frémond ML
Lung Inflammation in STING-Associated Vasculopathy with Onset in Infancy (SAVI)
David C et al. Lung Inflammation in STING-Associated Vasculopathy with Onset in Infancy (SAVI). . 2022-01-18. Pubmed ID: 35159128; DOI: 10.3390/cells11030318; PMC: PMC8834229 IMAGINi011-A 2022-01-18 2022-01-18 PubMed: 35159128 DOI: 10.3390/cells11030318Associated cell lines:
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Akol I, Gather F, Vogel T
Paving Therapeutic Avenues for FOXG1 Syndrome: Untangling Genotypes and Phenotypes from a Molecular Perspective
Akol I et al. Paving Therapeutic Avenues for FOXG1 Syndrome: Untangling Genotypes and Phenotypes from a Molecular Perspective. . 2022-01-16. Pubmed ID: 35055139; DOI: 10.3390/ijms23020954; PMC: PMC8780739 DCGi001-A 2022-01-16 2022-01-16 PubMed: 35055139 DOI: 10.3390/ijms23020954Associated cell lines:
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Akhtar BM, Bhatia P, Acharya S, Sharma S, Sharma Y, Bhuvanendran Nair Suseela Devi A, Ganapathy K, Vasudevan A, Raghu P
A human stem cell resource to decipher the biochemical and cellular basis of neurodevelopmental defects in Lowe syndrome
Akhtar BM et al. A human stem cell resource to decipher the biochemical and cellular basis of neurodevelopmental defects in Lowe syndrome. . 2022-01-15. Pubmed ID: 35023542; DOI: 10.1242/bio.059066; PMC: PMC8822356 SDUBMSi009-AWMUi031-A 2022-01-15 2022-01-15 PubMed: 35023542 DOI: 10.1242/bio.059066Associated cell lines:
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Nouri P, Zimmer A, Brüggemann S, Friedrich R, Kühn R, Prakash N
Generation of a NES-mScarlet Red Fluorescent Reporter Human iPSC Line for Live Cell Imaging and Flow Cytometric Analysis and Sorting Using CRISPR-Cas9-Mediated Gene Editing
Nouri P et al. Generation of a NES-mScarlet Red Fluorescent Reporter Human iPSC Line for Live Cell Imaging and Flow Cytometric Analysis and Sorting Using CRISPR-Cas9-Mediated Gene Editing. . 2022-01-13. Pubmed ID: 35053384; DOI: 10.3390/cells11020268; PMC: PMC8773741 KSCBi005-AKSCBi005-A-1 2022-01-13 2022-01-13 PubMed: 35053384 DOI: 10.3390/cells11020268Associated cell lines:
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Ulivieri A, Lavra L, Magi F, Morgante A, Calò L, Polisca P, Salehi LB, Sciacchitano S
Thyroid hormones regulate cardiac repolarization and QT-interval related gene expression in hiPSC cardiomyocytes
Ulivieri A et al. Thyroid hormones regulate cardiac repolarization and QT-interval related gene expression in hiPSC cardiomyocytes. . 2022-01-12. Pubmed ID: 35022468; DOI: 10.1038/s41598-021-04659-w; PMC: PMC8755773 NCUFi001-A 2022-01-12 2022-01-12 PubMed: 35022468 DOI: 10.1038/s41598-021-04659-wAssociated cell lines:
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Aldrin-Kirk P, Åkerblom M, Cardoso T, Nolbrant S, Adler AF, Liu X, Heuer A, Davidsson M, Parmar M, Björklund T
A novel two-factor monosynaptic TRIO tracing method for assessment of circuit integration of hESC-derived dopamine transplants
Aldrin-Kirk P et al. A novel two-factor monosynaptic TRIO tracing method for assessment of circuit integration of hESC-derived dopamine transplants. . 2022-01-11. Pubmed ID: 34971563; DOI: 10.1016/j.stemcr.2021.11.014; PMC: PMC8758947 RCe021-A 2022-01-11 2022-01-11 PubMed: 34971563 DOI: 10.1016/j.stemcr.2021.11.014Associated cell lines:
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Raabe FJ, Stephan M, Waldeck JB, Huber V, Demetriou D, Kannaiyan N, Galinski S, Glaser LV, Wehr MC, Ziller MJ, Schmitt A, Falkai P, Rossner MJ
Expression of Lineage Transcription Factors Identifies Differences in Transition States of Induced Human Oligodendrocyte Differentiation
Raabe FJ et al. Expression of Lineage Transcription Factors Identifies Differences in Transition States of Induced Human Oligodendrocyte Differentiation. . 2022-01-11. Pubmed ID: 35053357; DOI: 10.3390/cells11020241; PMC: PMC8773672 PSYLMUi001-APSYLMUi002-APSYLMUi003-APSYLMUi006-APSYLMUi023-APSYLMUi027-A 2022-01-11 2022-01-11 PubMed: 35053357 DOI: 10.3390/cells11020241Associated cell lines:
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de Leeuw SM, Kirschner AWT, Lindner K, Rust R, Budny V, Wolski WE, Gavin AC, Nitsch RM, Tackenberg C
APOE2, E3, and E4 differentially modulate cellular homeostasis, cholesterol metabolism, and inflammatory response in isogenic iPSC-derived astrocytes
de Leeuw SM et al. APOE2, E3, and E4 differentially modulate cellular homeostasis, cholesterol metabolism, and inflammatory response in isogenic iPSC-derived astrocytes. . 2022-01-11. Pubmed ID: 34919811; DOI: 10.1016/j.stemcr.2021.11.007; PMC: PMC8758949 BIONi010-CBIONi010-C-2BIONi010-C-3BIONi010-C-4BIONi010-C-6 2022-01-11 2022-01-11 PubMed: 34919811 DOI: 10.1016/j.stemcr.2021.11.007Associated cell lines:
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Yan Q, Wulfridge P, Doherty J, Fernandez-Luna JL, Real PJ, Tang HY, Sarma K
Proximity labeling identifies a repertoire of site-specific R-loop modulators
Yan Q et al. Proximity labeling identifies a repertoire of site-specific R-loop modulators. . 2022-01-10. Pubmed ID: 35013239; DOI: 10.1038/s41467-021-27722-6; PMC: PMC8748879 GENYOi004-A 2022-01-10 2022-01-10 PubMed: 35013239 DOI: 10.1038/s41467-021-27722-6Associated cell lines:
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Tabakov V. Yu.
Management of biobanking for medical genetics research
Tabakov V. Yu.. Management of biobanking for medical genetics research. . 2022-01-09. DOI: 10.15829/1728-8800-2021-3027 RCMGi002-A 2022-01-09 2022-01-09 DOI: 10.15829/1728-8800-2021-3027Associated cell lines:
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Pozo MR, Meredith GW, Entcheva E
Human iPSC-Cardiomyocytes as an Experimental Model to Study Epigenetic Modifiers of Electrophysiology
Pozo MR et al. Human iPSC-Cardiomyocytes as an Experimental Model to Study Epigenetic Modifiers of Electrophysiology. . 2022-01-07. Pubmed ID: 35053315; DOI: 10.3390/cells11020200; PMC: PMC8774228 MHHi001-AMHHi001-A-5 2022-01-07 2022-01-07 PubMed: 35053315 DOI: 10.3390/cells11020200Associated cell lines:
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Mianné J, Nasri A, Van CN, Bourguignon C, Fieldès M, Ahmed E, Duthoit C, Martin N, Parrinello H, Louis A, Iché A, Gayon R, Samain F, Lamouroux L, Bouillé P, Bourdin A, Assou S, De Vos J
CRISPR/Cas9-mediated gene knockout and interallelic gene conversion in human induced pluripotent stem cells using non-integrative bacteriophage-chimeric retrovirus-like particles
Mianné J et al. CRISPR/Cas9-mediated gene knockout and interallelic gene conversion in human induced pluripotent stem cells using non-integrative bacteriophage-chimeric retrovirus-like particles. . 2022-01-07. Pubmed ID: 34996449; DOI: 10.1186/s12915-021-01214-x; PMC: PMC8742436 UHOMi001-AUHOMi002-A 2022-01-07 2022-01-07 PubMed: 34996449 DOI: 10.1186/s12915-021-01214-xAssociated cell lines:
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Fisch D, Clough B, Khan R, Healy L, Frickel EM
Toxoplasma-proximal and distal control by GBPs in human macrophages
Fisch D et al. Toxoplasma-proximal and distal control by GBPs in human macrophages. . 2022-01-07. Pubmed ID: 34931666; DOI: 10.1093/femspd/ftab058; PMC: PMC8752258 WTSIi018-BWTSIi018-B-1 2022-01-07 2022-01-07 PubMed: 34931666 DOI: 10.1093/femspd/ftab058Associated cell lines:
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Grekhnev DA, Kaznacheyeva EV, Vigont VA
Patient-Specific iPSCs-Based Models of Neurodegenerative Diseases: Focus on Aberrant Calcium Signaling
Grekhnev DA et al. Patient-Specific iPSCs-Based Models of Neurodegenerative Diseases: Focus on Aberrant Calcium Signaling. . 2022-01-06. Pubmed ID: 35054808; DOI: 10.3390/ijms23020624; PMC: PMC8776084 RCPCMi008-A 2022-01-06 2022-01-06 PubMed: 35054808 DOI: 10.3390/ijms23020624Associated cell lines:
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Bartolomé A
Stem Cell-Derived β Cells: A Versatile Research Platform to Interrogate the Genetic Basis of β Cell Dysfunction
Bartolomé A. Stem Cell-Derived β Cells: A Versatile Research Platform to Interrogate the Genetic Basis of β Cell Dysfunction. . 2022-01-02. Pubmed ID: 35008927; DOI: 10.3390/ijms23010501; PMC: PMC8745644 HVRDe008-AHVRDe008-A-1 2022-01-02 2022-01-02 PubMed: 35008927 DOI: 10.3390/ijms23010501Associated cell lines:
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Perepelina K, Zaytseva A, Khudiakov A, Neganova I, Vasichkina E, Malashicheva A, Kostareva A.
LMNA mutation leads to cardiac sodium channel dysfunction in the Emery-Dreifuss muscular dystrophy patient
Perepelina K et al. LMNA mutation leads to cardiac sodium channel dysfunction in the Emery-Dreifuss muscular dystrophy patient. . 2022-01-01. WTSIi004-AFAMRCi007-A 2022-01-01 2022-01-01Associated cell lines:
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Nouri P, Zimmer A, Brüggemann S, Friedrich R, Kühn R, Prakash N.
Generation of a NES-mScarlet Red Fluorescent Reporter Human iPSC Line for Live Cell Imaging and Flow Cytometric Analysis and Sorting Using CRISPR-Cas9-Mediated Gene Editing
Nouri P et al. Generation of a NES-mScarlet Red Fluorescent Reporter Human iPSC Line for Live Cell Imaging and Flow Cytometric Analysis and Sorting Using CRISPR-Cas9-Mediated Gene Editing. . 2022-01-01. KSCBi005-AKSCBi005-A-1 2022-01-01 2022-01-01Associated cell lines:
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Sang W.
Application and research progress of human induced pluripotent stem cell in cardiovascular disease
Sang W.. Application and research progress of human induced pluripotent stem cell in cardiovascular disease. . 2022-01-01. DOI: 10.20039/j.cnki.1007-3949.2022.12.002 EHTJUi004-A 2022-01-01 2022-01-01 DOI: 10.20039/j.cnki.1007-3949.2022.12.002Associated cell lines:
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Zhao H.
Research advances of hyperlipidemic pancreatitis
Zhao H.. Research advances of hyperlipidemic pancreatitis. . 2022-01-01. DOI: 10.12290/xhyxzz.2021-0760 AHQUi001-AAHQUi001-A-1 2022-01-01 2022-01-01 DOI: 10.12290/xhyxzz.2021-0760Associated cell lines:
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Sutharshan G.S.
STEM CELLS AND ITS MULTIMODALITY - A REVIEW
Sutharshan G.S.. STEM CELLS AND ITS MULTIMODALITY - A REVIEW. . 2022-01-01. DOI: 10.47750/pnr.2022.13.s04.151 CMCi006-ACMCi007-ACMCi009-A 2022-01-01 2022-01-01 DOI: 10.47750/pnr.2022.13.s04.151 -
Giovenale A, Ruotolo G, Soriano A, Turco E, Rotundo G, Casamassa A, D’Anzi A, Vescovi A, Rosati J.
Deepening the understanding of CNVs on chromosome 15q11–13 by using hiPSCs: An overview
Giovenale A et al. Deepening the understanding of CNVs on chromosome 15q11–13 by using hiPSCs: An overview. . 2022-01-01. BIONi010-ABIONi010-BBIONi010-C 2022-01-01 2022-01-01Associated cell lines:
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Zhang F, Meier A, Poch C, Tian Q, Engelhardt S, Sinnecker D, Lipp P, Laugwitz K, Moretti A, Dorn T.
High-throughput optical action potential recordings in hiPSC-derived cardiomyocytes with a genetically encoded voltage indicator in the AAVS1 locus
Zhang F et al. High-throughput optical action potential recordings in hiPSC-derived cardiomyocytes with a genetically encoded voltage indicator in the AAVS1 locus. . 2022-01-01. MRIi003-AMRIi003-A-5MRIi003-A-6 2022-01-01 2022-01-01Associated cell lines:
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Frøslev P, Franzyk H, Ozgür B, Brodin B, Kristensen M
Highly cationic cell-penetrating peptides affect the barrier integrity and facilitates mannitol permeation in a human stem cell-based blood-brain barrier model
Frøslev P et al. Highly cationic cell-penetrating peptides affect the barrier integrity and facilitates mannitol permeation in a human stem cell-based blood-brain barrier model. . 2022-01-01. Pubmed ID: 34728364; DOI: 10.1016/j.ejps.2021.106054 BIONi010-C 2022-01-01 2022-01-01 PubMed: 34728364 DOI: 10.1016/j.ejps.2021.106054Associated cell lines:
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Oh S, Niwa A, Nagahashi A, Asaka I, Nakahata T, Saito MK
iPS cells from Chediak-Higashi syndrome patients recapitulate the giant granules in myeloid cells
Oh S et al. iPS cells from Chediak-Higashi syndrome patients recapitulate the giant granules in myeloid cells. . 2022-01-00. Pubmed ID: 36259166; DOI: 10.1111/ped.15390 SANi007-A 2022-01-00 2022-01-00 PubMed: 36259166 DOI: 10.1111/ped.15390Associated cell lines:
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Wang G, Gao E, Wu H, Zhang L, Zhu Y, Zhang J, Liu Z
Establishment of the induced pluripotent stem cell line (NCKDi005-A) from a male patient with Alport syndrome carrying a homozygous frameshift mutation in the COL4A4 gene
Wang G et al. Establishment of the induced pluripotent stem cell line (NCKDi005-A) from a male patient with Alport syndrome carrying a homozygous frameshift mutation in the COL4A4 gene. . 2022-01-00. Pubmed ID: 34942480; DOI: 10.1016/j.scr.2021.102628 NCKDi005-A 2022-01-00 2022-01-00 PubMed: 34942480 DOI: 10.1016/j.scr.2021.102628Associated cell lines:
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Larizza L, Calzari L, Alari V, Russo S
Genes for RNA-binding proteins involved in neural-specific functions and diseases are downregulated in Rubinstein-Taybi iNeurons
Larizza L et al. Genes for RNA-binding proteins involved in neural-specific functions and diseases are downregulated in Rubinstein-Taybi iNeurons. . 2022-01-00. Pubmed ID: 34100419; DOI: 10.4103/1673-5374.314286; PMC: PMC8451555 IAIi001-A 2022-01-00 2022-01-00 PubMed: 34100419 DOI: 10.4103/1673-5374.314286Associated cell lines:
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Ader F, Duboscq-Bidot L, Marteau S, Hamlin M, Richard P, Fontaine V, Villard E
Generation of CRISPR-Cas9 edited human induced pluripotent stem cell line carrying FLNC exon skipping variant
Ader F et al. Generation of CRISPR-Cas9 edited human induced pluripotent stem cell line carrying FLNC exon skipping variant. . 2022-01-00. Pubmed ID: 34883448; DOI: 10.1016/j.scr.2021.102616 ICANi002-AICANi002-A-1 2022-01-00 2022-01-00 PubMed: 34883448 DOI: 10.1016/j.scr.2021.102616Associated cell lines:
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Yan W, Wang Y, Ye Q, Chen X, Chen Y, Jiang C, Chen M
The electrophysiological features of X-linked juvenile retinoschisis in a young male: a case report
Yan W et al. The electrophysiological features of X-linked juvenile retinoschisis in a young male: a case report. . 2022-01-00. Pubmed ID: 34994217; DOI: 10.1177/03000605211039571; PMC: PMC8743956 CSUASOi005-A 2022-01-00 2022-01-00 PubMed: 34994217 DOI: 10.1177/03000605211039571Associated cell lines:
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Veraldi N, Dentand Quadri I, de Agostini A
Characterization of a spontaneous cell line from primary mouse fibroblasts as a model to study Sanfilippo syndrome
Veraldi N et al. Characterization of a spontaneous cell line from primary mouse fibroblasts as a model to study Sanfilippo syndrome. . 2022-01-00. Pubmed ID: 34823007; DOI: 10.1016/j.biocel.2021.106119 IMEDEAi004-AIMEDEAi004-B 2022-01-00 2022-01-00 PubMed: 34823007 DOI: 10.1016/j.biocel.2021.106119Associated cell lines:
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Colbert BM, Gosstola NC, Dykxhoorn DM, Zhong Liu X
Generation of hiPSC line UMi030-A from an individual with the hearing loss-related GJB2 mutation c.109G > A
Colbert BM et al. Generation of hiPSC line UMi030-A from an individual with the hearing loss-related GJB2 mutation c.109G > A. . 2022-01-00. Pubmed ID: 34883447; DOI: 10.1016/j.scr.2021.102599 UMi030-A 2022-01-00 2022-01-00 PubMed: 34883447 DOI: 10.1016/j.scr.2021.102599Associated cell lines:
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Dong Y, Li X, Fu W, Tian X, Guo G, Peng Y, Zhai Y, Zhao J, Ding Z, Zhao X, Dong J
Generation of an iPSC line (ZZUNEUi021-A) from a hypertrophic cardiomyopathy patient with TNNT2 mutation
Dong Y et al. Generation of an iPSC line (ZZUNEUi021-A) from a hypertrophic cardiomyopathy patient with TNNT2 mutation. . 2022-01-00. Pubmed ID: 34929444; DOI: 10.1016/j.scr.2021.102622 ZZUNEUi021-A 2022-01-00 2022-01-00 PubMed: 34929444 DOI: 10.1016/j.scr.2021.102622Associated cell lines:
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Huang XR, Tang BS, Jin P, Guo JF
The Phenotypes and Mechanisms of NOTCH2NLC-Related GGC Repeat Expansion Disorders: a Comprehensive Review
Huang XR et al. The Phenotypes and Mechanisms of NOTCH2NLC-Related GGC Repeat Expansion Disorders: a Comprehensive Review. . 2022-01-00. Pubmed ID: 34718964; DOI: 10.1007/s12035-021-02616-2 ZZUi020-A 2022-01-00 2022-01-00 PubMed: 34718964 DOI: 10.1007/s12035-021-02616-2Associated cell lines:
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Zhang Q, Wang Z, Sun H, Chen N, Xu X, Yang J, Gao Y, Wang Y, Xu Y
Corrigendum to "Generation of induced pluripotent stem cell line (ZZUi030-A) from a patient with spastic paraplegia type 7" [Stem Cell Res. 56 (2021) 102525]
Zhang Q et al. Corrigendum to "Generation of induced pluripotent stem cell line (ZZUi030-A) from a patient with spastic paraplegia type 7" [Stem Cell Res. 56 (2021) 102525]. . 2022-01-00. Pubmed ID: 34922242; DOI: 10.1016/j.scr.2021.102619 ZZUi030-A 2022-01-00 2022-01-00 PubMed: 34922242 DOI: 10.1016/j.scr.2021.102619Associated cell lines:
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Cerrizuela S, Vega-Lopez GA, Méndez-Maldonado K, Velasco I, Aybar MJ
The crucial role of model systems in understanding the complexity of cell signaling in human neurocristopathies
Cerrizuela S et al. The crucial role of model systems in understanding the complexity of cell signaling in human neurocristopathies. . 2022-01-00. Pubmed ID: 35023327; DOI: 10.1002/wsbm.1537 IDISi001-AJTUi002-ABGUi004-ABGUi005-ACSUXHi003-ASDQLCHi037-A 2022-01-00 2022-01-00 PubMed: 35023327 DOI: 10.1002/wsbm.1537Associated cell lines:
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Cakmak Cagla, Zempel Hans
A perspective on human cell models for POLG-spectrum disorders: advantages and disadvantages of CRISPR-Cas-based vs. patient-derived iPSC models
Cakmak Cagla et al. A perspective on human cell models for POLG-spectrum disorders: advantages and disadvantages of CRISPR-Cas-based vs. patient-derived iPSC models. . 2021-12-31. DOI: 10.1515/medgen-2021-2090 UKWNLi001-A 2021-12-31 2021-12-31 DOI: 10.1515/medgen-2021-2090Associated cell lines:
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Magusali N, Graham AC, Piers TM, Panichnantakul P, Yaman U, Shoai M, Reynolds RH, Botia JA, Brookes KJ, Guetta-Baranes T, Bellou E, Bayram S, Sokolova D, Ryten M, Sala Frigerio C, Escott-Price V, Morgan K, Pocock JM, Hardy J, Salih DA
A genetic link between risk for Alzheimer's disease and severe COVID-19 outcomes via the OAS1 gene
Magusali N et al. A genetic link between risk for Alzheimer's disease and severe COVID-19 outcomes via the OAS1 gene. . 2021-12-31. Pubmed ID: 34619763; DOI: 10.1093/brain/awab337; PMC: PMC8500089 BIONi010-C 2021-12-31 2021-12-31 PubMed: 34619763 DOI: 10.1093/brain/awab337Associated cell lines:
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Mossink B, van Rhijn JR, Wang S, Linda K, Vitale MR, Zöller JEM, van Hugte EJH, Bak J, Verboven AHA, Selten M, Negwer M, Latour BL, van der Werf I, Keller JM, Klein Gunnewiek TM, Schoenmaker C, Oudakker A, Anania A, Jansen S, Lesch KP, Frega M, van Bokhoven H, Schubert D, Nadif Kasri N
Cadherin-13 is a critical regulator of GABAergic modulation in human stem-cell-derived neuronal networks
Mossink B et al. Cadherin-13 is a critical regulator of GABAergic modulation in human stem-cell-derived neuronal networks. . 2022-01-00. Pubmed ID: 33972691; DOI: 10.1038/s41380-021-01117-x; PMC: PMC8960401 UKWMPi002-AUKWMPi002-A-1UKWMPi002-A-2 2022-01-00 2022-01-00 PubMed: 33972691 DOI: 10.1038/s41380-021-01117-xAssociated cell lines:
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Dreßen M, Lahm H, Neb I, Luzius T, Doppler SA, Schneider S, Dzilic E, Lange R, Krane M
Establishment of a patient-specific induced pluripotent stem cell line DHMi004-A from a male Holt-Oram syndrome patient with verified TBX5 mutation
Dreßen M et al. Establishment of a patient-specific induced pluripotent stem cell line DHMi004-A from a male Holt-Oram syndrome patient with verified TBX5 mutation. . 2022-01-00. Pubmed ID: 34894535; DOI: 10.1016/j.scr.2021.102617 DHMi004-A 2022-01-00 2022-01-00 PubMed: 34894535 DOI: 10.1016/j.scr.2021.102617Associated cell lines:
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Li T, Sun H, Wang Z, Zhang Q, Chen N, Zhang K, Wang Y, Xu Y
Generation of induced pluripotent stem cell line (ZZUi015-A) from a DM1 patient with cataract
Li T et al. Generation of induced pluripotent stem cell line (ZZUi015-A) from a DM1 patient with cataract. . 2022-01-00. Pubmed ID: 34915310; DOI: 10.1016/j.scr.2021.102623 CHUQi001-AZZUi005-AZZUi015-A 2022-01-00 2022-01-00 PubMed: 34915310 DOI: 10.1016/j.scr.2021.102623Associated cell lines:
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Canac R, Caillaud A, Cimarosti B, Girardeau A, Hamamy H, Reversade B, Bonnard C, Al Sayed ZR, David L, Poschmann J, Lemarchand P, Lamirault G, Gaborit N
Generation of three human induced pluripotent stem cell lines with IRX5 knockout and knockin genetic editions using CRISPR-Cas9 system
Canac R et al. Generation of three human induced pluripotent stem cell lines with IRX5 knockout and knockin genetic editions using CRISPR-Cas9 system. . 2022-01-00. Pubmed ID: 34929443; DOI: 10.1016/j.scr.2021.102627 ITXi002-AITXi002-A-1ITXi002-A-2ITXi002-A-3 2022-01-00 2022-01-00 PubMed: 34929443 DOI: 10.1016/j.scr.2021.102627Associated cell lines:
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Zhang C, Shi J, Zhang Z, Zhao Q, Xie M, Chen Y, Xiang Q
Generation of an induced pluripotent stem cell line (SYSUi005-A) from a patient with hypertrophic cardiomyopathy
Zhang C et al. Generation of an induced pluripotent stem cell line (SYSUi005-A) from a patient with hypertrophic cardiomyopathy. . 2022-01-00. Pubmed ID: 34942479; DOI: 10.1016/j.scr.2021.102626 SYSUi005-A 2022-01-00 2022-01-00 PubMed: 34942479 DOI: 10.1016/j.scr.2021.102626Associated cell lines:
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Fagerlund I, Dougalis A, Shakirzyanova A, Gómez-Budia M, Pelkonen A, Konttinen H, Ohtonen S, Fazaludeen MF, Koskuvi M, Kuusisto J, Hernández D, Pebay A, Koistinaho J, Rauramaa T, Lehtonen Š, Korhonen P, Malm T
Microglia-like Cells Promote Neuronal Functions in Cerebral Organoids
Fagerlund I et al. Microglia-like Cells Promote Neuronal Functions in Cerebral Organoids. . 2021-12-30. Pubmed ID: 35011686; DOI: 10.3390/cells11010124; PMC: PMC8750120 BIONi010-CBIONi010-C-2 2021-12-30 2021-12-30 PubMed: 35011686 DOI: 10.3390/cells11010124Associated cell lines:
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Zhang Xiaolong, Wang Hongyang, Wang Qiuju
Progression of KCNQ4 related genetic hearing loss: a narrative review
Zhang Xiaolong et al. Progression of KCNQ4 related genetic hearing loss: a narrative review. . 2021-12-30. DOI: 10.1097/jbr.0000000000000112 CPGHi001-A 2021-12-30 2021-12-30 DOI: 10.1097/jbr.0000000000000112Associated cell lines:
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Kasi DG, de Graaf MNS, Motreuil-Ragot PA, Frimat JMS, Ferrari MD, Sarro PM, Mastrangeli M, van den Maagdenberg AMJM, Mummery CL, Orlova VV
Rapid Prototyping of Organ-on-a-Chip Devices Using Maskless Photolithography
Kasi DG et al. Rapid Prototyping of Organ-on-a-Chip Devices Using Maskless Photolithography. . 2021-12-29. Pubmed ID: 35056214; DOI: 10.3390/mi13010049; PMC: PMC8778126 LUMCi001-ALUMCi002-ALUMCi003-ALUMCi028-A 2021-12-29 2021-12-29 PubMed: 35056214 DOI: 10.3390/mi13010049Associated cell lines:
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Sasson E, Anzi S, Bell B, Yakovian O, Zorsky M, Deutsch U, Engelhardt B, Sherman E, Vatine G, Dzikowski R, Ben-Zvi A
Nano-scale architecture of blood-brain barrier tight-junctions
Sasson E et al. Nano-scale architecture of blood-brain barrier tight-junctions. . 2021-12-24. Pubmed ID: 34951586; DOI: 10.7554/elife.63253; PMC: PMC8747500 BGUi004-ABGUi005-ABGUi012-A 2021-12-24 2021-12-24 PubMed: 34951586 DOI: 10.7554/elife.63253 -
Barbarics B, Eildermann K, Kaderali L, Cyganek L, Plessmann U, Bodemeyer J, Paul T, Ströbel P, Urlaub H, Tirilomis T, Lenz C, Bohnenberger H
Proteomic mapping of atrial and ventricular heart tissue in patients with aortic valve stenosis
Barbarics B et al. Proteomic mapping of atrial and ventricular heart tissue in patients with aortic valve stenosis. . 2021-12-22. Pubmed ID: 34937869; DOI: 10.1038/s41598-021-03907-3; PMC: PMC8695579 UMGi001-AUMGi014-A 2021-12-22 2021-12-22 PubMed: 34937869 DOI: 10.1038/s41598-021-03907-3 -
Manstein F, Ullmann K, Triebert W, Zweigerdt R
Process control and in silico modeling strategies for enabling high density culture of human pluripotent stem cells in stirred tank bioreactors
Manstein F et al. Process control and in silico modeling strategies for enabling high density culture of human pluripotent stem cells in stirred tank bioreactors. . 2021-12-17. Pubmed ID: 34917976; DOI: 10.1016/j.xpro.2021.100988; PMC: PMC8666714 MHHi001-AMHHi006-AMHHi008-A 2021-12-17 2021-12-17 PubMed: 34917976 DOI: 10.1016/j.xpro.2021.100988 -
Mérien A, Tahraoui-Bories J, Cailleret M, Dupont JB, Leteur C, Polentes J, Carteron A, Polvèche H, Concordet JP, Pinset C, Jarrige M, Furling D, Martinat C
CRISPR gene editing in pluripotent stem cells reveals the function of MBNL proteins during human in vitro myogenesis
Mérien A et al. CRISPR gene editing in pluripotent stem cells reveals the function of MBNL proteins during human in vitro myogenesis. . 2021-12-17. Pubmed ID: 34312665; DOI: 10.1093/hmg/ddab218; PMC: PMC8682758 ZZUi006-A 2021-12-17 2021-12-17 PubMed: 34312665 DOI: 10.1093/hmg/ddab218Associated cell lines:
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Besikcioglu HE, Yurteri Ü, Munkhbaatar E, Ye L, Zhang F, Moretti A, Mota Reyes C, Özoğul C, Friess H, Ceyhan GO, Istvanffy R, Demir IE
Innervated mouse pancreas organoids as an ex vivo model to study pancreatic neuropathy in pancreatic cancer
Besikcioglu HE et al. Innervated mouse pancreas organoids as an ex vivo model to study pancreatic neuropathy in pancreatic cancer. . 2021-12-17. Pubmed ID: 34841274; DOI: 10.1016/j.xpro.2021.100935; PMC: PMC8605431 BIONi014-A 2021-12-17 2021-12-17 PubMed: 34841274 DOI: 10.1016/j.xpro.2021.100935Associated cell lines:
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Io S, Iemura Y, Takashima Y
Optimized protocol for naive human pluripotent stem cell-derived trophoblast induction
Io S et al. Optimized protocol for naive human pluripotent stem cell-derived trophoblast induction. . 2021-12-17. Pubmed ID: 34761233; DOI: 10.1016/j.xpro.2021.100921; PMC: PMC8567437 WAe009-ACAMi004-A 2021-12-17 2021-12-17 PubMed: 34761233 DOI: 10.1016/j.xpro.2021.100921 -
Pantazis Caroline B., Yang Andrian, Lara Erika, McDonough Justin A., Blauwendraat Cornelis, Peng Lirong, Oguro Hideyuki, Kanaujiya Jitendra, Zou Jizhong, Sebesta David, Pratt Gretchen, Cross Erin, Blockwick Jeffrey, Buxton Philip, Kinner-Bibeau Lauren, Medura Constance, Tompkins Christopher, Hughes Stephen, Santiana Marianita, Faghri Faraz, Nalls Mike A., Vitale Daniel, Ballard Shannon, Qi Yue A., Ramos Daniel M., Anderson Kailyn M., Stadler Julia, Narayan Priyanka, Papademetriou Jason, Reilly Luke, Nelson Matthew P., Aggarwal Sanya, Rosen Leah U., Kirwan Peter, Pisupati Venkat, Coon Steven L., Scholz Sonja W., Priebe Theresa, Öttl Miriam, Dong Jian, Meijer Marieke, Janssen Lara J.M., Lourenco Vanessa S., van der Kant Rik, Crusius Dennis, Paquet Dominik, Raulin Ana-Caroline, Bu Guojun, Held Aaron, Wainger Brian J., Gabriele Rebecca M.C., Casey Jackie M, Wray Selina, Abu-Bonsrah Dad, Parish Clare L., Beccari Melinda S., Cleveland Don W., Li Emmy, Rose Indigo V.L., Kampmann Martin, Aristoy Carles Calatayud, Verstreken Patrik, Heinrich Laurin, Chen Max Y., Schüle Birgitt, Dou Dan, Holzbaur Erika L.F., Zanellati Maria Clara, Basundra Richa, Deshmukh Mohanish, Cohen Sarah, Khanna Richa, Raman Malavika, Nevin Zachary S., Matia Madeline, Lent Jonas Van, Timmerman Vincent, Conklin Bruce R., Chase Katherine Johnson, Zhang Ke, Funes Salome, Bosco Daryl A., Erlebach Lena, Welzer Marc, Kronenberg-Versteeg Deborah, Lyu Guochang, Arenas Ernest, Coccia Elena, Sarrafha Lily, Ahfeldt Tim, Marioni John C., Skarnes William C., Cookson Mark R., Ward Michael E., Merkle Florian T.
A reference induced pluripotent stem cell line for large-scale collaborative studies
Pantazis Caroline B. et al. A reference induced pluripotent stem cell line for large-scale collaborative studies. . 2021-12-17. DOI: 10.1101/2021.12.15.472643 WTSIi018-B-1 2021-12-17 2021-12-17 DOI: 10.1101/2021.12.15.472643Associated cell lines:
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Abstracts from the Virtual Symposium "Signal Transduction at the Blood-Brain Barriers"
(unknown author). Abstracts from the Virtual Symposium "Signal Transduction at the Blood-Brain Barriers". . 2021-12-17. Pubmed ID: 34915908; DOI: 10.1186/s12987-021-00286-9; PMC: PMC8677339 BIONi010-C 2021-12-17 2021-12-17 PubMed: 34915908 DOI: 10.1186/s12987-021-00286-9Associated cell lines:
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Memon B, Abdelalim EM
Differentiation of Human Pluripotent Stem Cells into Pancreatic Beta-cell Precursors in a 2D Culture System
Memon B et al. Differentiation of Human Pluripotent Stem Cells into Pancreatic Beta-cell Precursors in a 2D Culture System. . 2021-12-16. Pubmed ID: 34978292; DOI: 10.3791/63298 QBRIi009-A 2021-12-16 2021-12-16 PubMed: 34978292 DOI: 10.3791/63298Associated cell lines:
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Fiorenzano A, Sozzi E, Birtele M, Kajtez J, Giacomoni J, Nilsson F, Bruzelius A, Sharma Y, Zhang Y, Mattsson B, Emnéus J, Ottosson DR, Storm P, Parmar M
Single-cell transcriptomics captures features of human midbrain development and dopamine neuron diversity in brain organoids
Fiorenzano A et al. Single-cell transcriptomics captures features of human midbrain development and dopamine neuron diversity in brain organoids. . 2021-12-15. Pubmed ID: 34911939; DOI: 10.1038/s41467-021-27464-5; PMC: PMC8674361 WAe009-ARCe021-A 2021-12-15 2021-12-15 PubMed: 34911939 DOI: 10.1038/s41467-021-27464-5 -
Shi H.
Analysis of Gene Carrier and Characteristics for Neonatal Thalassemia in Baisha Li Autonomous County, Hainan Province in 2020
Shi H.. Analysis of Gene Carrier and Characteristics for Neonatal Thalassemia in Baisha Li Autonomous County, Hainan Province in 2020. . 2021-12-15. DOI: 10.12114/j.issn.1007-9572.2021.01.401 HNMUi002-AHNMUi003-AHNMUi004-AHNMUi005-AHNMUi006-AHNMUi007-AHNMUi008-AHNMUi009-AHNMUi010-A 2021-12-15 2021-12-15 DOI: 10.12114/j.issn.1007-9572.2021.01.401Associated cell lines:
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Tristan CA, Ormanoglu P, Slamecka J, Malley C, Chu PH, Jovanovic VM, Gedik Y, Jethmalani Y, Bonney C, Barnaeva E, Braisted J, Mallanna SK, Dorjsuren D, Iannotti MJ, Voss TC, Michael S, Simeonov A, Singeç I
Robotic high-throughput biomanufacturing and functional differentiation of human pluripotent stem cells
Tristan CA et al. Robotic high-throughput biomanufacturing and functional differentiation of human pluripotent stem cells. . 2021-12-14. Pubmed ID: 34861164; DOI: 10.1016/j.stemcr.2021.11.004; PMC: PMC8693769 WAe009-ARUCDRi002-A 2021-12-14 2021-12-14 PubMed: 34861164 DOI: 10.1016/j.stemcr.2021.11.004Associated cell lines:
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Schaniel C, Dhanan P, Hu B, Xiong Y, Raghunandan T, Gonzalez DM, Dariolli R, D'Souza SL, Yadaw AS, Hansen J, Jayaraman G, Mathew B, Machado M, Berger SI, Tripodi J, Najfeld V, Garg J, Miller M, Surlyn CS, Michelis KC, Tangirala NC, Weerahandi H, Thomas DC, Beaumont KG, Sebra R, Mahajan M, Schadt E, Vidovic D, Schürer SC, Goldfarb J, Azeloglu EU, Birtwistle MR, Sobie EA, Kovacic JC, Dubois NC, Iyengar R
A library of induced pluripotent stem cells from clinically well-characterized, diverse healthy human individuals
Schaniel C et al. A library of induced pluripotent stem cells from clinically well-characterized, diverse healthy human individuals. . 2021-12-14. Pubmed ID: 34739849; DOI: 10.1016/j.stemcr.2021.10.005; PMC: PMC8693622 ISMMSi004-AISMMSi005-AISMMSi006-AISMMSi007-AISMMSi008-AISMMSi009-AISMMSi010-AISMMSi011-AISMMSi012-AISMMSi013-AISMMSi014-AISMMSi015-AISMMSi016-AISMMSi017-AISMMSi017-BISMMSi017-CISMMSi018-AISMMSi019-AISMMSi020-AISMMSi021-AISMMSi022-AISMMSi023-AISMMSi024-AISMMSi025-AISMMSi026-AISMMSi027-AISMMSi028-AISMMSi028-BISMMSi028-CISMMSi029-AISMMSi030-AISMMSi031-AISMMSi032-AISMMSi033-AISMMSi034-AISMMSi035-AISMMSi036-AISMMSi037-AISMMSi038-AISMMSi039-AISMMSi040-AISMMSi041-AISMMSi042-AISMMSi043-A 2021-12-14 2021-12-14 PubMed: 34739849 DOI: 10.1016/j.stemcr.2021.10.005 -
Castro-Viñuelas R, Sanjurjo-Rodríguez C, Piñeiro-Ramil M, Rodríguez-Fernández S, López-Baltar I, Fuentes-Boquete I, Blanco FJ, Díaz-Prado S
Tips and tricks for successfully culturing and adapting human induced pluripotent stem cells
Castro-Viñuelas R et al. Tips and tricks for successfully culturing and adapting human induced pluripotent stem cells. . 2021-12-10. Pubmed ID: 34901305; DOI: 10.1016/j.omtm.2021.10.013; PMC: PMC8640166 ESi080-A 2021-12-10 2021-12-10 PubMed: 34901305 DOI: 10.1016/j.omtm.2021.10.013Associated cell lines:
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Barabás K, Kobolák J, Godó S, Kovács T, Ernszt D, Kecskés M, Varga C, Jánosi TZ, Fujiwara T, Kusumi A, Téglási A, Dinnyés A, Ábrahám IM
Live-Cell Imaging of Single Neurotrophin Receptor Molecules on Human Neurons in Alzheimer's Disease
Barabás K et al. Live-Cell Imaging of Single Neurotrophin Receptor Molecules on Human Neurons in Alzheimer's Disease. . 2021-12-09. Pubmed ID: 34948057; DOI: 10.3390/ijms222413260; PMC: PMC8708879 BIOTi001-A 2021-12-09 2021-12-09 PubMed: 34948057 DOI: 10.3390/ijms222413260Associated cell lines:
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Bekhite MM, Schulze PC
Human Induced Pluripotent Stem Cell as a Disease Modeling and Drug Development Platform-A Cardiac Perspective
Bekhite MM et al. Human Induced Pluripotent Stem Cell as a Disease Modeling and Drug Development Platform-A Cardiac Perspective. . 2021-12-09. Pubmed ID: 34943991; DOI: 10.3390/cells10123483; PMC: PMC8699880 ISMMSi002-BTRNDi003-A 2021-12-09 2021-12-09 PubMed: 34943991 DOI: 10.3390/cells10123483Associated cell lines:
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Kang EY, Liu PK, Wen YT, Quinn PMJ, Levi SR, Wang NK, Tsai RK
Role of Oxidative Stress in Ocular Diseases Associated with Retinal Ganglion Cells Degeneration
Kang EY et al. Role of Oxidative Stress in Ocular Diseases Associated with Retinal Ganglion Cells Degeneration. . 2021-12-05. Pubmed ID: 34943051; DOI: 10.3390/antiox10121948; PMC: PMC8750806 IISHDOi003-A 2021-12-05 2021-12-05 PubMed: 34943051 DOI: 10.3390/antiox10121948Associated cell lines:
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Singh S, Singh T, Kunja C, Dhoat NS, Dhania NK
Gene-editing, immunological and iPSCs based therapeutics for muscular dystrophy
Singh S et al. Gene-editing, immunological and iPSCs based therapeutics for muscular dystrophy. . 2021-12-05. Pubmed ID: 34656607; DOI: 10.1016/j.ejphar.2021.174568 FAMRCi006-AFAMRCi006-B 2021-12-05 2021-12-05 PubMed: 34656607 DOI: 10.1016/j.ejphar.2021.174568Associated cell lines:
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Schlattner U
The Complex Functions of the NME Family-A Matter of Location and Molecular Activity
Schlattner U. The Complex Functions of the NME Family-A Matter of Location and Molecular Activity. . 2021-12-03. Pubmed ID: 34884887; DOI: 10.3390/ijms222313083; PMC: PMC8658066 MHHi019-AMHHi019-B 2021-12-03 2021-12-03 PubMed: 34884887 DOI: 10.3390/ijms222313083 -
Sandilya S, Singh S
Development of islet organoids from human induced pluripotent stem cells in a cross-linked collagen scaffold
Sandilya S et al. Development of islet organoids from human induced pluripotent stem cells in a cross-linked collagen scaffold. . 2021-12-01. Pubmed ID: 34850295; DOI: 10.1186/s13619-021-00099-z; PMC: PMC8633270 CCMBi001-A 2021-12-01 2021-12-01 PubMed: 34850295 DOI: 10.1186/s13619-021-00099-zAssociated cell lines:
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Fang J, Zhang P, Zhou Y, Chiang C, Tan J, Hou Y, Stauffer S, Li L, Pieper A, Cummings J, Cheng F.
Endophenotype-based in silico network medicine discovery combined with insurance record data mining identifies sildenafil as a candidate drug for Alzheimer’s disease
Fang J et al. Endophenotype-based in silico network medicine discovery combined with insurance record data mining identifies sildenafil as a candidate drug for Alzheimer’s disease. . 2021-12-01. HVRDi001-A-1 2021-12-01 2021-12-01Associated cell lines:
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Xiao W, Shen Y, Xu Y
LOX(G473A) induces the formation of osteoclasts in RAW264.7 cells via IL-6/JAK2/STAT3 signaling
Xiao W et al. LOX(G473A) induces the formation of osteoclasts in RAW264.7 cells via IL-6/JAK2/STAT3 signaling. . 2021-12-01. Pubmed ID: 34695437; DOI: 10.1016/j.yexcr.2021.112890 JUCTCi012-A 2021-12-01 2021-12-01 PubMed: 34695437 DOI: 10.1016/j.yexcr.2021.112890Associated cell lines:
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Zhang F, Meier AB, Laugwitz KL, Dorn T, Moretti A
Generation of heterozygous (MRli003-A-1) and homozygous (MRli003-A-2) MYH10 knockout human iPSC lines
Zhang F et al. Generation of heterozygous (MRli003-A-1) and homozygous (MRli003-A-2) MYH10 knockout human iPSC lines. . 2021-12-00. Pubmed ID: 34864222; DOI: 10.1016/j.scr.2021.102612 MRIi003-AMRIi003-A-1MRIi003-A-2 2021-12-00 2021-12-00 PubMed: 34864222 DOI: 10.1016/j.scr.2021.102612Associated cell lines:
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Mestrallet G, Carosella ED, Martin MT, Rouas-Freiss N, Fortunel NO, LeMaoult J
Immunosuppressive Properties of Epidermal Keratinocytes Differ According to Their Immaturity Status
Mestrallet G et al. Immunosuppressive Properties of Epidermal Keratinocytes Differ According to Their Immaturity Status. . 2022-00-00. Pubmed ID: 35222373; DOI: 10.3389/fimmu.2022.786859; PMC: PMC8878806 TCIERi001-A 2022-00-00 2022-00-00 PubMed: 35222373 DOI: 10.3389/fimmu.2022.786859Associated cell lines:
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Kloos D, Lachmann N
Generation of Human iPSC from Small Volume Peripheral Blood Samples
Kloos D et al. Generation of Human iPSC from Small Volume Peripheral Blood Samples. . 2022-00-00. Pubmed ID: 35507153; DOI: 10.1007/978-1-0716-1979-7_3 MHHi012-AMHHi013-AMHHi014-AMHHi018-A 2022-00-00 2022-00-00 PubMed: 35507153 DOI: 10.1007/978-1-0716-1979-7_3 -
Lehmann RJ, Jolly LA, Johnson BV, Lord MS, Kim HN, Saville JT, Fuller M, Byers S, Derrick-Roberts ALK
Impaired neural differentiation of MPS IIIA patient induced pluripotent stem cell-derived neural progenitor cells
Lehmann RJ et al. Impaired neural differentiation of MPS IIIA patient induced pluripotent stem cell-derived neural progenitor cells. . 2021-12-00. Pubmed ID: 34712574; DOI: 10.1016/j.ymgmr.2021.100811; PMC: PMC8531667 IMEDEAi004-AIMEDEAi004-BTRNDi005-A 2021-12-00 2021-12-00 PubMed: 34712574 DOI: 10.1016/j.ymgmr.2021.100811Associated cell lines:
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Kiris E
Human-Induced Pluripotent Stem Cell-Based Models for Studying Sex-Specific Differences in Neurodegenerative Diseases
Kiris E. Human-Induced Pluripotent Stem Cell-Based Models for Studying Sex-Specific Differences in Neurodegenerative Diseases. . 2022-00-00. Pubmed ID: 34921676; DOI: 10.1007/5584_2021_683 METUi001-A 2022-00-00 2022-00-00 PubMed: 34921676 DOI: 10.1007/5584_2021_683Associated cell lines:
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Liu M, Ge N, Han Y, Reilly J, Yang M, Yang F, Krawczyk J, McInerney V, O'Brien T, Prendiville T, Shen S
Generation and characterization of three induced pluripotent stem cell lines (NUIGi046-A, NUIGi046-B, NUIGi046-C) from a 51-year-old healthy individual
Liu M et al. Generation and characterization of three induced pluripotent stem cell lines (NUIGi046-A, NUIGi046-B, NUIGi046-C) from a 51-year-old healthy individual. . 2021-12-00. Pubmed ID: 34844101; DOI: 10.1016/j.scr.2021.102607 NUIGi038-ANUIGi038-BNUIGi046-ANUIGi046-BNUIGi046-C 2021-12-00 2021-12-00 PubMed: 34844101 DOI: 10.1016/j.scr.2021.102607Associated cell lines:
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Panda Naresh Kumar, Sharma Maryada, Ramavat Anurag Snehi, Patro Sourabha Kumar, Nayak Gyan Ranjan, Kaushal Kavita
Novel Cellular Stress Models with Implications in Understanding and Treating ENT Pathologies
Panda Naresh Kumar et al. Novel Cellular Stress Models with Implications in Understanding and Treating ENT Pathologies. . 2022-00-00. DOI: 10.1007/978-981-16-8845-4_7 CPGHi001-A 2022-00-00 2022-00-00 DOI: 10.1007/978-981-16-8845-4_7Associated cell lines:
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Guo T, Jiang Y, Song Y, Ma S, Chang Y, Zhang S, Wang H, Dong T, Jiang H, Lu W
Generation of a homozygous MYH7 gene knockout human embryonic stem cell line (WAe009-A-69) using an episomal vector-based CRISPR/Cas9 system
Guo T et al. Generation of a homozygous MYH7 gene knockout human embryonic stem cell line (WAe009-A-69) using an episomal vector-based CRISPR/Cas9 system. . 2021-12-00. Pubmed ID: 34678661; DOI: 10.1016/j.scr.2021.102566 WAe009-AWAe009-A-69 2021-12-00 2021-12-00 PubMed: 34678661 DOI: 10.1016/j.scr.2021.102566Associated cell lines:
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Sun J, Ou W, Han D, Paganini-Hill A, Fisher MJ, Sumbria RK
Comparative studies between the murine immortalized brain endothelial cell line (bEnd.3) and induced pluripotent stem cell-derived human brain endothelial cells for paracellular transport
Sun J et al. Comparative studies between the murine immortalized brain endothelial cell line (bEnd.3) and induced pluripotent stem cell-derived human brain endothelial cells for paracellular transport. . 2022-00-00. Pubmed ID: 35613139; DOI: 10.1371/journal.pone.0268860; PMC: PMC9132315 WISCi004-B 2022-00-00 2022-00-00 PubMed: 35613139 DOI: 10.1371/journal.pone.0268860Associated cell lines:
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Mollo N, Aurilia M, Scognamiglio R, Zerillo L, Cicatiello R, Bonfiglio F, Pagano P, Paladino S, Conti A, Nitsch L, Izzo A
Overexpression of the Hsa21 Transcription Factor RUNX1 Modulates the Extracellular Matrix in Trisomy 21 Cells
Mollo N et al. Overexpression of the Hsa21 Transcription Factor RUNX1 Modulates the Extracellular Matrix in Trisomy 21 Cells. . 2022-00-00. Pubmed ID: 35356434; DOI: 10.3389/fgene.2022.824922; PMC: PMC8960062 UNINAi001-AUNINAi002-A 2022-00-00 2022-00-00 PubMed: 35356434 DOI: 10.3389/fgene.2022.824922Associated cell lines:
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Liu T, Zhuang XX, Qin XJ, Wei LB, Gao JR
Identifying effective diagnostic biomarkers and immune infiltration features in chronic kidney disease by bioinformatics and validation
Liu T et al. Identifying effective diagnostic biomarkers and immune infiltration features in chronic kidney disease by bioinformatics and validation. . 2022-00-00. Pubmed ID: 36642989; DOI: 10.3389/fphar.2022.1069810; PMC: PMC9838551 SDQLCHi040-A 2022-00-00 2022-00-00 PubMed: 36642989 DOI: 10.3389/fphar.2022.1069810Associated cell lines:
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Lee Y, Koo SK, Kim JH
Establishment of a human-induced pluripotent stem cell line, KSCBi014-A, from a long QT syndrome type 2 patient harboring a KCNH2 mutation
Lee Y et al. Establishment of a human-induced pluripotent stem cell line, KSCBi014-A, from a long QT syndrome type 2 patient harboring a KCNH2 mutation. . 2021-12-00. Pubmed ID: 34678663; DOI: 10.1016/j.scr.2021.102570 KSCBi005-AKSCBi005-A-1KSCBi014-A 2021-12-00 2021-12-00 PubMed: 34678663 DOI: 10.1016/j.scr.2021.102570Associated cell lines:
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Wang Y, Wang Z, Sun H, Zhang Q, Yang J, Liu Y, Liu H, Shi C, Zhang R, Xu Y
Corrigendum to "Generation of induced pluripotent stem cell line (ZZUi028-A) from a 52-year-old Chinese Han healthy female individual" [Stem Cell Res. 53 (2021) 102381]
Wang Y et al. Corrigendum to "Generation of induced pluripotent stem cell line (ZZUi028-A) from a 52-year-old Chinese Han healthy female individual" [Stem Cell Res. 53 (2021) 102381]. . 2021-12-00. Pubmed ID: 34801939; DOI: 10.1016/j.scr.2021.102603 ZZUi028-A 2021-12-00 2021-12-00 PubMed: 34801939 DOI: 10.1016/j.scr.2021.102603Associated cell lines:
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Zhang H, Chen J, Zhu Y, Ma X, Zhong W
Case Report: Identification of Compound Heterozygous Mutations in a Patient With Late-Onset Glycogen Storage Disease Type II (Pompe Disease)
Zhang H et al. Case Report: Identification of Compound Heterozygous Mutations in a Patient With Late-Onset Glycogen Storage Disease Type II (Pompe Disease). . 2022-00-00. Pubmed ID: 35386406; DOI: 10.3389/fneur.2022.839263; PMC: PMC8977516 TRNDi007-B 2022-00-00 2022-00-00 PubMed: 35386406 DOI: 10.3389/fneur.2022.839263Associated cell lines:
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Mou Yongchao, Chen Zhenyu, Li Xue-Jun
Modeling hereditary spastic paraplegias using induced pluripotent stem cells
Mou Yongchao et al. Modeling hereditary spastic paraplegias using induced pluripotent stem cells. . 2022-00-00. DOI: 10.1016/b978-0-323-85765-9.00006-0 FJMUi001-ASDUBMSi001-A 2022-00-00 2022-00-00 DOI: 10.1016/b978-0-323-85765-9.00006-0Associated cell lines:
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Wang L, Yang Z, He X, Pu S, Yang C, Wu Q, Zhou Z, Cen X, Zhao H
Mitochondrial protein dysfunction in pathogenesis of neurological diseases
Wang L et al. Mitochondrial protein dysfunction in pathogenesis of neurological diseases. . 2022-00-00. Pubmed ID: 36157077; DOI: 10.3389/fnmol.2022.974480; PMC: PMC9489860 JUCTCi019-A 2022-00-00 2022-00-00 PubMed: 36157077 DOI: 10.3389/fnmol.2022.974480Associated cell lines:
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Karvonen E, Krohn KJE, Ranki A, Hau A
Generation and Characterization of iPS Cells Derived from APECED Patients for Gene Correction
Karvonen E et al. Generation and Characterization of iPS Cells Derived from APECED Patients for Gene Correction. . 2022-00-00. Pubmed ID: 35432216; DOI: 10.3389/fendo.2022.794327; PMC: PMC9010864 UHi006-A 2022-00-00 2022-00-00 PubMed: 35432216 DOI: 10.3389/fendo.2022.794327Associated cell lines:
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Gillentine Madelyn A.
Exploring 15q13.3 copy number variants in iPSCs
Gillentine Madelyn A.. Exploring 15q13.3 copy number variants in iPSCs. . 2022-00-00. DOI: 10.1016/b978-0-323-99892-5.00017-7 CSSi005-A 2022-00-00 2022-00-00 DOI: 10.1016/b978-0-323-99892-5.00017-7Associated cell lines:
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Sintov E, Gerace D, Melton DA
A human ESC line for efficient CRISPR editing of pluripotent stem cells
Sintov E et al. A human ESC line for efficient CRISPR editing of pluripotent stem cells. . 2021-12-00. Pubmed ID: 34741877; DOI: 10.1016/j.scr.2021.102591 HVRDe008-AHVRDe008-A-1HVRDe008-A-2 2021-12-00 2021-12-00 PubMed: 34741877 DOI: 10.1016/j.scr.2021.102591Associated cell lines:
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Mehrabi M, Morris TA, Cang Z, Nguyen CHH, Sha Y, Asad MN, Khachikyan N, Greene TL, Becker DM, Nie Q, Zaragoza MV, Grosberg A
A Study of Gene Expression, Structure, and Contractility of iPSC-Derived Cardiac Myocytes from a Family with Heart Disease due to LMNA Mutation
Mehrabi M et al. A Study of Gene Expression, Structure, and Contractility of iPSC-Derived Cardiac Myocytes from a Family with Heart Disease due to LMNA Mutation. . 2021-12-00. Pubmed ID: 34585335; DOI: 10.1007/s10439-021-02850-8; PMC: PMC8671287 FAMRCi006-AFAMRCi006-BPUMCHi001-APUMCHi001-A-1 2021-12-00 2021-12-00 PubMed: 34585335 DOI: 10.1007/s10439-021-02850-8Associated cell lines:
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Romero JC, Berlinicke C, Chow S, Duan Y, Wang Y, Chamling X, Smirnova L
Oligodendrogenesis and myelination tracing in a CRISPR/Cas9-engineered brain microphysiological system
Romero JC et al. Oligodendrogenesis and myelination tracing in a CRISPR/Cas9-engineered brain microphysiological system. . 2022-00-00. Pubmed ID: 36744062; DOI: 10.3389/fncel.2022.1094291; PMC: PMC9893511 USCBi001-A 2022-00-00 2022-00-00 PubMed: 36744062 DOI: 10.3389/fncel.2022.1094291Associated cell lines:
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Li J, Zhang B, Gan M, Li Y, He L, Yue W, Qiao H, Pei X, Li Y
Generation of SHMT2 knockout human embryonic stem cell line (WAe009-A-67) using CRISPR/Cas9 technique
Li J et al. Generation of SHMT2 knockout human embryonic stem cell line (WAe009-A-67) using CRISPR/Cas9 technique. . 2021-12-00. Pubmed ID: 34688993; DOI: 10.1016/j.scr.2021.102581 WAe009-AWAe009-A-67 2021-12-00 2021-12-00 PubMed: 34688993 DOI: 10.1016/j.scr.2021.102581Associated cell lines:
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Zakharova I, Saaya S, Shevchenko A, Stupnikova A, Zhiven' M, Laktionov P, Stepanova A, Romashchenko A, Yanshole L, Chernonosov A, Volkov A, Kizilova E, Zavjalov E, Chernyavsky A, Romanov A, Karpenko A, Zakian S
Mitomycin-Treated Endothelial and Smooth Muscle Cells Suitable for Safe Tissue Engineering Approaches
Zakharova I et al. Mitomycin-Treated Endothelial and Smooth Muscle Cells Suitable for Safe Tissue Engineering Approaches. . 2022-00-00. Pubmed ID: 35360387; DOI: 10.3389/fbioe.2022.772981; PMC: PMC8963790 ICGi021-AICGi022-A 2022-00-00 2022-00-00 PubMed: 35360387 DOI: 10.3389/fbioe.2022.772981 -
Weng OY, Li Y, Wang LY
Modeling Epilepsy Using Human Induced Pluripotent Stem Cells-Derived Neuronal Cultures Carrying Mutations in Ion Channels and the Mechanistic Target of Rapamycin Pathway
Weng OY et al. Modeling Epilepsy Using Human Induced Pluripotent Stem Cells-Derived Neuronal Cultures Carrying Mutations in Ion Channels and the Mechanistic Target of Rapamycin Pathway. . 2022-00-00. Pubmed ID: 35359577; DOI: 10.3389/fnmol.2022.810081; PMC: PMC8960276 HIHDNEi002-AHIHDNEi003-A 2022-00-00 2022-00-00 PubMed: 35359577 DOI: 10.3389/fnmol.2022.810081Associated cell lines:
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Scholz S, Lewis K, Saulich F, Endres M, Boehmerle W, Huehnchen P
Induced pluripotent stem cell-derived brain organoids as potential human model system for chemotherapy induced CNS toxicity
Scholz S et al. Induced pluripotent stem cell-derived brain organoids as potential human model system for chemotherapy induced CNS toxicity. . 2022-00-00. Pubmed ID: 36188215; DOI: 10.3389/fmolb.2022.1006497; PMC: PMC9520921 BIHi250-A 2022-00-00 2022-00-00 PubMed: 36188215 DOI: 10.3389/fmolb.2022.1006497Associated cell lines:
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Alich TC, Röderer P, Szalontai B, Golcuk K, Tariq S, Peitz M, Brüstle O, Mody I
Bringing to light the physiological and pathological firing patterns of human induced pluripotent stem cell-derived neurons using optical recordings
Alich TC et al. Bringing to light the physiological and pathological firing patterns of human induced pluripotent stem cell-derived neurons using optical recordings. . 2022-00-00. Pubmed ID: 36733665; DOI: 10.3389/fncel.2022.1039957; PMC: PMC9887032 RCi001-AUKBi013-A 2022-00-00 2022-00-00 PubMed: 36733665 DOI: 10.3389/fncel.2022.1039957 -
Solman M, Woutersen DTJ, den Hertog J
Modeling (not so) rare developmental disorders associated with mutations in the protein-tyrosine phosphatase SHP2
Solman M et al. Modeling (not so) rare developmental disorders associated with mutations in the protein-tyrosine phosphatase SHP2. . 2022-00-00. Pubmed ID: 36407105; DOI: 10.3389/fcell.2022.1046415; PMC: PMC9672471 TRNDi003-A 2022-00-00 2022-00-00 PubMed: 36407105 DOI: 10.3389/fcell.2022.1046415Associated cell lines:
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Zhang F, Meier AB, Poch CM, Tian Q, Engelhardt S, Sinnecker D, Lipp P, Laugwitz KL, Moretti A, Dorn T
High-throughput optical action potential recordings in hiPSC-derived cardiomyocytes with a genetically encoded voltage indicator in the AAVS1 locus
Zhang F et al. High-throughput optical action potential recordings in hiPSC-derived cardiomyocytes with a genetically encoded voltage indicator in the AAVS1 locus. . 2022-00-00. Pubmed ID: 36274846; DOI: 10.3389/fcell.2022.1038867; PMC: PMC9585323 MRIi003-AMRIi003-A-5MRIi003-A-6 2022-00-00 2022-00-00 PubMed: 36274846 DOI: 10.3389/fcell.2022.1038867Associated cell lines:
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Wang Y, Fang Y, Zhang D, Li Y, Luo S
A rare case of arrhythmogenic right ventricular cardiomyopathy associated with LAMA2 mutation: A case report and literature review
Wang Y et al. A rare case of arrhythmogenic right ventricular cardiomyopathy associated with LAMA2 mutation: A case report and literature review. . 2022-00-00. Pubmed ID: 35924034; DOI: 10.3389/fmed.2022.922347; PMC: PMC9339636 WCHi002-A 2022-00-00 2022-00-00 PubMed: 35924034 DOI: 10.3389/fmed.2022.922347Associated cell lines:
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Souralova Tereza, Rehakova Daniela, Tesarova Lenka, Hampl Ales, Koutna Irena
Characterization of Clinical-Grade Stem Cells: Microscopic, Cellular, Molecular, and Functional Characterization of Stem Cells and Their Products According to Regulatory Requirements for FDA Approval
Souralova Tereza et al. Characterization of Clinical-Grade Stem Cells: Microscopic, Cellular, Molecular, and Functional Characterization of Stem Cells and Their Products According to Regulatory Requirements for FDA Approval. . 2022-00-00. DOI: 10.1007/978-981-16-7589-8_8 RCe013-A 2022-00-00 2022-00-00 DOI: 10.1007/978-981-16-7589-8_8Associated cell lines:
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Jeriha J, Kolundzic N, Khurana P, Perez-Dominguez A, Ilic D
mRNA-Based Reprogramming Under Xeno-Free and Feeder-Free Conditions
Jeriha J et al. mRNA-Based Reprogramming Under Xeno-Free and Feeder-Free Conditions. . 2022-00-00. Pubmed ID: 32567019; DOI: 10.1007/7651_2020_302 KCLi002-AKCLi003-A 2022-00-00 2022-00-00 PubMed: 32567019 DOI: 10.1007/7651_2020_302 -
Schuster J, de Guidi C, Fatima A, Sobol M, Dahl N
Syndromic RNA polymerase II insufficiency: Generation of a human induced pluripotent stem cell line (UUIGPi002A-5) with a heterozygous disruption of POLR2A
Schuster J et al. Syndromic RNA polymerase II insufficiency: Generation of a human induced pluripotent stem cell line (UUIGPi002A-5) with a heterozygous disruption of POLR2A. . 2021-12-00. Pubmed ID: 34688129; DOI: 10.1016/j.scr.2021.102577 KICRi002-A-5 2021-12-00 2021-12-00 PubMed: 34688129 DOI: 10.1016/j.scr.2021.102577Associated cell lines:
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Shahryari Alireza, Nazari Zahra, Jazi Marie Saghaeian, Hashemi-Shahraki Fatemeh, Wißmiller Katharina, Xu Weiwei, Burtscher Ingo, Lickert Heiko
Gene Therapy
Shahryari Alireza et al. Gene Therapy. . 2022-00-00. DOI: 10.1016/b978-0-12-820472-6.00213-9 HMGUi001-AHMGUi001-A-5 2022-00-00 2022-00-00 DOI: 10.1016/b978-0-12-820472-6.00213-9Associated cell lines:
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Romano E, Trionfini P, Giampietro R, Benigni A, Tomasoni S
Generation of a homozygous CIITA knockout iPS cell line using the CRISPR-Cas9 system
Romano E et al. Generation of a homozygous CIITA knockout iPS cell line using the CRISPR-Cas9 system. . 2021-12-00. Pubmed ID: 34688128; DOI: 10.1016/j.scr.2021.102580; PMC: PMC8665218 IRFMNi001-BIRFMNi001-B-1IRFMNi001-B-2 2021-12-00 2021-12-00 PubMed: 34688128 DOI: 10.1016/j.scr.2021.102580Associated cell lines:
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Murganti F, Derks W, Baniol M, Simonova I, Trus P, Neumann K, Khattak S, Guan K, Bergmann O
FUCCI-Based Live Imaging Platform Reveals Cell Cycle Dynamics and Identifies Pro-proliferative Compounds in Human iPSC-Derived Cardiomyocytes
Murganti F et al. FUCCI-Based Live Imaging Platform Reveals Cell Cycle Dynamics and Identifies Pro-proliferative Compounds in Human iPSC-Derived Cardiomyocytes. . 2022-00-00. Pubmed ID: 35548410; DOI: 10.3389/fcvm.2022.840147; PMC: PMC9081338 CRTDi005-B 2022-00-00 2022-00-00 PubMed: 35548410 DOI: 10.3389/fcvm.2022.840147Associated cell lines:
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Ramamurthy RM, Rodriguez M, Ainsworth HC, Shields J, Meares D, Bishop C, Farland A, Langefeld CD, Atala A, Doering CB, Spencer HT, Porada CD, Almeida-Porada G
Comparison of different gene addition strategies to modify placental derived-mesenchymal stromal cells to produce FVIII
Ramamurthy RM et al. Comparison of different gene addition strategies to modify placental derived-mesenchymal stromal cells to produce FVIII. . 2022-00-00. Pubmed ID: 36591257; DOI: 10.3389/fimmu.2022.954984; PMC: PMC9800010 YCMi001-BYCMi001-B-1 2022-00-00 2022-00-00 PubMed: 36591257 DOI: 10.3389/fimmu.2022.954984Associated cell lines:
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Kelekçi S, Yıldız AB, Sevinç K, Çimen DU, Önder T
Perspectives on current models of Friedreich's ataxia
Kelekçi S et al. Perspectives on current models of Friedreich's ataxia. . 2022-00-00. Pubmed ID: 36036008; DOI: 10.3389/fcell.2022.958398; PMC: PMC9403045 USFi001-A 2022-00-00 2022-00-00 PubMed: 36036008 DOI: 10.3389/fcell.2022.958398Associated cell lines:
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Wang X, Zhang S, Hu S, Xu H, Zhang Q, Tang W
Establishment of an induced pluripotent stem cell line (ZZUPMCi001-A) derived from peripheral blood mononuclear cells in a patient with type 1 Waardenburg syndrome
Wang X et al. Establishment of an induced pluripotent stem cell line (ZZUPMCi001-A) derived from peripheral blood mononuclear cells in a patient with type 1 Waardenburg syndrome. . 2021-12-00. Pubmed ID: 34864221; DOI: 10.1016/j.scr.2021.102606 ZZUPMCi001-A 2021-12-00 2021-12-00 PubMed: 34864221 DOI: 10.1016/j.scr.2021.102606Associated cell lines:
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Lee H, Lee JJ, Park NY, Dubey SK, Kim T, Ruan K, Lim SB, Park SH, Ha S, Kovlyagina I, Kim KT, Kim S, Oh Y, Kim H, Kang SU, Song MR, Lloyd TE, Maragakis NJ, Hong YB, Eoh H, Lee G
Multi-omic analysis of selectively vulnerable motor neuron subtypes implicates altered lipid metabolism in ALS
Lee H et al. Multi-omic analysis of selectively vulnerable motor neuron subtypes implicates altered lipid metabolism in ALS. . 2021-12-00. Pubmed ID: 34782793; DOI: 10.1038/s41593-021-00944-z; PMC: PMC8639773 FRIMOi001-A 2021-12-00 2021-12-00 PubMed: 34782793 DOI: 10.1038/s41593-021-00944-zAssociated cell lines:
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Escribá R, Ferrer-Lorente R, Raya Á
Inborn errors of metabolism: Lessons from iPSC models
Escribá R et al. Inborn errors of metabolism: Lessons from iPSC models. . 2021-12-00. Pubmed ID: 34241766; DOI: 10.1007/s11154-021-09671-z; PMC: PMC8724155 TRNDi007-B 2021-12-00 2021-12-00 PubMed: 34241766 DOI: 10.1007/s11154-021-09671-zAssociated cell lines:
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Moita MR, Silva MM, Diniz C, Serra M, Hoet RM, Barbas A, Simão D
Transcriptome and proteome profiling of activated cardiac fibroblasts supports target prioritization in cardiac fibrosis
Moita MR et al. Transcriptome and proteome profiling of activated cardiac fibroblasts supports target prioritization in cardiac fibrosis. . 2022-00-00. Pubmed ID: 36531712; DOI: 10.3389/fcvm.2022.1015473; PMC: PMC9751336 UCSFi001-AUCSFi001-A-19 2022-00-00 2022-00-00 PubMed: 36531712 DOI: 10.3389/fcvm.2022.1015473Associated cell lines:
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Wang R, Bai X, Yang H, Ma J, Yu S, Lu Z
Identification of a novel AIFM1 variant from a Chinese family with auditory neuropathy
Wang R et al. Identification of a novel AIFM1 variant from a Chinese family with auditory neuropathy. . 2022-00-00. Pubmed ID: 36479253; DOI: 10.3389/fgene.2022.1064823; PMC: PMC9721464 CPGHi001-A 2022-00-00 2022-00-00 PubMed: 36479253 DOI: 10.3389/fgene.2022.1064823Associated cell lines:
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Liu Y, Liu X, Huang M, Zhang L, Lu J, Zhang Z, Ding X
Generation of induced pluripotent stem cell (iPSC) line ZOCi003-A derived from peripheral blood mononuclear cells of X-linked juvenile retinoschisis harboring a hemizygous mutation in RS1 gene
Liu Y et al. Generation of induced pluripotent stem cell (iPSC) line ZOCi003-A derived from peripheral blood mononuclear cells of X-linked juvenile retinoschisis harboring a hemizygous mutation in RS1 gene. . 2021-12-00. Pubmed ID: 34798543; DOI: 10.1016/j.scr.2021.102595 ZOCi002-A 2021-12-00 2021-12-00 PubMed: 34798543 DOI: 10.1016/j.scr.2021.102595Associated cell lines:
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Arendzen CH, Chaudhari U, Cramer SJ, Freund CMAH, Mummery CL, Ranga A, Pourquie O, Mikkers HMM
Generation of LUMCi041-A-2: Equipping a PAX3 reporter iPSC line with doxycycline inducible H2B-mTurquoise2 for live cell imaging
Arendzen CH et al. Generation of LUMCi041-A-2: Equipping a PAX3 reporter iPSC line with doxycycline inducible H2B-mTurquoise2 for live cell imaging. . 2021-12-00. Pubmed ID: 34775202; DOI: 10.1016/j.scr.2021.102592 CRMi003-A-2 2021-12-00 2021-12-00 PubMed: 34775202 DOI: 10.1016/j.scr.2021.102592Associated cell lines:
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Yu X, Yuan L, Deng S, Xia H, Tu X, Deng X, Huang X, Cao X, Deng H
Identification of DNAH17 Variants in Han-Chinese Patients With Left-Right Asymmetry Disorders
Yu X et al. Identification of DNAH17 Variants in Han-Chinese Patients With Left-Right Asymmetry Disorders. . 2022-00-00. Pubmed ID: 35692830; DOI: 10.3389/fgene.2022.862292; PMC: PMC9186109 MHHi019-AMHHi019-B 2022-00-00 2022-00-00 PubMed: 35692830 DOI: 10.3389/fgene.2022.862292 -
Sun L, Huang Y, Zhao S, Zhong W, Shi J, Guo Y, Zhao J, Xiong G, Yin Y, Chen Z, Zhang N, Zhao Z, Li Q, Chen D, Niu Y, Li X, Qiu G, Wu Z, Zhang TJ, Tian W, Wu N
Identification of Novel FBN2 Variants in a Cohort of Congenital Contractural Arachnodactyly
Sun L et al. Identification of Novel FBN2 Variants in a Cohort of Congenital Contractural Arachnodactyly. . 2022-00-00. Pubmed ID: 35360850; DOI: 10.3389/fgene.2022.804202; PMC: PMC8960307 HELPi001-A 2022-00-00 2022-00-00 PubMed: 35360850 DOI: 10.3389/fgene.2022.804202Associated cell lines:
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Zhang Q, Yang Q, Zhou X, Qin Z, Yi S, Luo J
Characteristics of Allan-Herndon-Dudley Syndrome in Chinese children: Identification of two novel pathogenic variants of the SLC16A2 gene
Zhang Q et al. Characteristics of Allan-Herndon-Dudley Syndrome in Chinese children: Identification of two novel pathogenic variants of the SLC16A2 gene. . 2022-00-00. Pubmed ID: 36458135; DOI: 10.3389/fped.2022.1050023; PMC: PMC9705582 SHCDNi003-A 2022-00-00 2022-00-00 PubMed: 36458135 DOI: 10.3389/fped.2022.1050023Associated cell lines:
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Zhang W, Li Y, Wang L, Xin T, Zhang C
Generation of a DKK2 homozygous knockout human embryonic stem cell line using the CRISPR/Cas9 system
Zhang W et al. Generation of a DKK2 homozygous knockout human embryonic stem cell line using the CRISPR/Cas9 system. . 2021-12-00. Pubmed ID: 34856466; DOI: 10.1016/j.scr.2021.102611 SYSUe011-A-1 2021-12-00 2021-12-00 PubMed: 34856466 DOI: 10.1016/j.scr.2021.102611Associated cell lines:
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Dettmer R, Niwolik I, Mehmeti I, Jörns A, Naujok O
New hPSC SOX9 and INS Reporter Cell Lines Facilitate the Observation and Optimization of Differentiation into Insulin-Producing Cells
Dettmer R et al. New hPSC SOX9 and INS Reporter Cell Lines Facilitate the Observation and Optimization of Differentiation into Insulin-Producing Cells. . 2021-12-00. Pubmed ID: 34415483; DOI: 10.1007/s12015-021-10232-9; PMC: PMC8599335 MHHi001-AMHHi001-A-12 2021-12-00 2021-12-00 PubMed: 34415483 DOI: 10.1007/s12015-021-10232-9Associated cell lines:
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Shin Y, Mun SJ, Lee J, Chung KS, Kim M, Kun Cheon C, Son MJ
Generation of human induced pluripotent stem cell line, KRIBBi003-A, from urinary cells of a patient with glycogen storage disease type IXa
Shin Y et al. Generation of human induced pluripotent stem cell line, KRIBBi003-A, from urinary cells of a patient with glycogen storage disease type IXa. . 2021-12-00. Pubmed ID: 34740118; DOI: 10.1016/j.scr.2021.102584 KRIBBi003-A 2021-12-00 2021-12-00 PubMed: 34740118 DOI: 10.1016/j.scr.2021.102584Associated cell lines:
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Gao L, Shi C, Lin Q, Wu Y, Hu L, Wang M, Guan J, Lin S, Liao Y, Wu C
Case Report: A case of PLA2G6 gene-related early-onset Parkinson's disease and review of literature
Gao L et al. Case Report: A case of PLA2G6 gene-related early-onset Parkinson's disease and review of literature. . 2022-00-00. Pubmed ID: 36570855; DOI: 10.3389/fnins.2022.1064566; PMC: PMC9780693 IBMSi012-A 2022-00-00 2022-00-00 PubMed: 36570855 DOI: 10.3389/fnins.2022.1064566Associated cell lines:
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Chen H, Lyu JJ, Huang Z, Sun XM, Liu Y, Yuan CJ, Ye L, Yu D, Wu J
Case Report: Fanconi-Bickel Syndrome in a Chinese Girl With Diabetes and Severe Hypokalemia
Chen H et al. Case Report: Fanconi-Bickel Syndrome in a Chinese Girl With Diabetes and Severe Hypokalemia. . 2022-00-00. Pubmed ID: 35757134; DOI: 10.3389/fped.2022.897636; PMC: PMC9218529 QBRIi007-A 2022-00-00 2022-00-00 PubMed: 35757134 DOI: 10.3389/fped.2022.897636Associated cell lines:
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Zhou Q, Yao S, Yang M, Guo Q, Li Y, Li L, Lei B
Superoxide dismutase 2 ameliorates mitochondrial dysfunction in skin fibroblasts of Leber's hereditary optic neuropathy patients
Zhou Q et al. Superoxide dismutase 2 ameliorates mitochondrial dysfunction in skin fibroblasts of Leber's hereditary optic neuropathy patients. . 2022-00-00. Pubmed ID: 36017189; DOI: 10.3389/fnins.2022.917348; PMC: PMC9398213 FINCBi001-A 2022-00-00 2022-00-00 PubMed: 36017189 DOI: 10.3389/fnins.2022.917348Associated cell lines:
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Wang T, Zhang J, Liu J, Lai X
Generation of a heterozygous SOX10 knockout human embryonic stem cell line using CRISPR/Cas9 technology
Wang T et al. Generation of a heterozygous SOX10 knockout human embryonic stem cell line using CRISPR/Cas9 technology. . 2021-12-00. Pubmed ID: 34678662; DOI: 10.1016/j.scr.2021.102567 WAe009-A-71 2021-12-00 2021-12-00 PubMed: 34678662 DOI: 10.1016/j.scr.2021.102567Associated cell lines:
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Daoutsali E, Pepers BA, Stamatakis S, van der Graaf LM, Terwindt GM, Parfitt DA, Buijsen RAM, van Roon-Mom WMC
Amyloid beta accumulations and enhanced neuronal differentiation in cerebral organoids of Dutch-type cerebral amyloid angiopathy patients
Daoutsali E et al. Amyloid beta accumulations and enhanced neuronal differentiation in cerebral organoids of Dutch-type cerebral amyloid angiopathy patients. . 2022-00-00. Pubmed ID: 36733499; DOI: 10.3389/fnagi.2022.1048584; PMC: PMC9887998 LUMCi005-A 2022-00-00 2022-00-00 PubMed: 36733499 DOI: 10.3389/fnagi.2022.1048584Associated cell lines:
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Guo Wei, Wang Mingzi, Qin Zhenhua, Shen Xu, Lü Shulin, Chen Xiaohua, Wu Shusen
Improving the glass-forming ability and plasticity of a TiCu-based bulk metallic glass composite by minor Ta doping
Guo Wei et al. Improving the glass-forming ability and plasticity of a TiCu-based bulk metallic glass composite by minor Ta doping. . 2021-12-00. DOI: 10.1016/j.jallcom.2021.161054 GIBHi002-AGIBHi002-A-2 2021-12-00 2021-12-00 DOI: 10.1016/j.jallcom.2021.161054Associated cell lines:
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Ma Z, Toledo MAS, Wanek P, Elsafi Mabrouk MH, Smet F, Pulak R, Pieske S, Piotrowski T, Herfs W, Brecher C, Schmitt RH, Wagner W, Zenke M
Cell Cluster Sorting in Automated Differentiation of Patient-specific Induced Pluripotent Stem Cells Towards Blood Cells
Ma Z et al. Cell Cluster Sorting in Automated Differentiation of Patient-specific Induced Pluripotent Stem Cells Towards Blood Cells. . 2022-00-00. Pubmed ID: 35662848; DOI: 10.3389/fbioe.2022.755983; PMC: PMC9157239 UKAi004-BUKAi004-D 2022-00-00 2022-00-00 PubMed: 35662848 DOI: 10.3389/fbioe.2022.755983 -
Espinal ER, Sharp SJ, Kim BJ
Induced Pluripotent Stem Cell (iPSC)-Derived Endothelial Cells to Study Bacterial-Brain Endothelial Cell Interactions
Espinal ER et al. Induced Pluripotent Stem Cell (iPSC)-Derived Endothelial Cells to Study Bacterial-Brain Endothelial Cell Interactions. . 2022-00-00. Pubmed ID: 35733039; DOI: 10.1007/978-1-0716-2289-6_4 BIONi010-C 2022-00-00 2022-00-00 PubMed: 35733039 DOI: 10.1007/978-1-0716-2289-6_4Associated cell lines:
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Kowalski WJ, Garcia-Pak IH, Li W, Uosaki H, Tampakakis E, Zou J, Lin Y, Patterson K, Kwon C, Mukouyama YS
Sympathetic Neurons Regulate Cardiomyocyte Maturation in Culture
Kowalski WJ et al. Sympathetic Neurons Regulate Cardiomyocyte Maturation in Culture. . 2022-00-00. Pubmed ID: 35359438; DOI: 10.3389/fcell.2022.850645; PMC: PMC8961983 NHLBIi003-ANHLBIi003-A-1NHLBIi003-A-2 2022-00-00 2022-00-00 PubMed: 35359438 DOI: 10.3389/fcell.2022.850645Associated cell lines:
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Song D, Zheng YW, Hemmi Y, An Y, Noguchi M, Nakamura Y, Oda T, Hayashi Y
Generation of human induced pluripotent stem cell lines carrying homozygous JAG1 deletions
Song D et al. Generation of human induced pluripotent stem cell lines carrying homozygous JAG1 deletions. . 2021-12-00. Pubmed ID: 34736037; DOI: 10.1016/j.scr.2021.102588 UCSFi001-A-58UCSFi001-A-59 2021-12-00 2021-12-00 PubMed: 34736037 DOI: 10.1016/j.scr.2021.102588Associated cell lines:
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Novikoff Silviene, Câmara Niels Olsen Saraiva, Semedo-Kuriki Patricia
Stem Cells: Use in Nephrology
Novikoff Silviene et al. Stem Cells: Use in Nephrology. . 2022-00-00. DOI: 10.1007/978-3-031-11570-7_3 ZJUi007-A 2022-00-00 2022-00-00 DOI: 10.1007/978-3-031-11570-7_3Associated cell lines:
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Thamodaran V, Rani S, Velayudhan SR
Gene Editing in Human Induced Pluripotent Stem Cells Using Doxycycline-Inducible CRISPR-Cas9 System
Thamodaran V et al. Gene Editing in Human Induced Pluripotent Stem Cells Using Doxycycline-Inducible CRISPR-Cas9 System. . 2022-00-00. Pubmed ID: 33830454; DOI: 10.1007/7651_2021_348; PMC: PMC7612904 CSCRi005-A 2022-00-00 2022-00-00 PubMed: 33830454 DOI: 10.1007/7651_2021_348Associated cell lines:
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Lan MY, Lu CS, Wu SL, Chen YF, Sung YF, Tu MC, Chang YY
Clinical and genetic characterization of a Taiwanese cohort with spastic paraparesis combined with cerebellar involvement
Lan MY et al. Clinical and genetic characterization of a Taiwanese cohort with spastic paraparesis combined with cerebellar involvement. . 2022-00-00. Pubmed ID: 36247768; DOI: 10.3389/fneur.2022.1005670; PMC: PMC9563621 FJMUi001-A 2022-00-00 2022-00-00 PubMed: 36247768 DOI: 10.3389/fneur.2022.1005670Associated cell lines:
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Ramovs V, Fuentes I, Freund C, Mikkers H, Mummery CL, Raymond K
Generation and genetic repair of two human induced pluripotent cell lines from patients with Epidermolysis Bullosa simplex and dilated cardiomyopathy associated with a heterozygous mutation in the translation initiation codon of KLHL24
Ramovs V et al. Generation and genetic repair of two human induced pluripotent cell lines from patients with Epidermolysis Bullosa simplex and dilated cardiomyopathy associated with a heterozygous mutation in the translation initiation codon of KLHL24. . 2021-12-00. Pubmed ID: 34688992; DOI: 10.1016/j.scr.2021.102582 LUMCi045-ALUMCi045-A-1LUMCi046-ALUMCi046-A-1 2021-12-00 2021-12-00 PubMed: 34688992 DOI: 10.1016/j.scr.2021.102582Associated cell lines:
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Begentas OC, Koc D, Kiris E
Establishment of Human Induced Pluripotent Stem Cells from Multiple Sclerosis Patients
Begentas OC et al. Establishment of Human Induced Pluripotent Stem Cells from Multiple Sclerosis Patients. . 2022-00-00. Pubmed ID: 34988943; DOI: 10.1007/7651_2021_453 METUi001-A 2022-00-00 2022-00-00 PubMed: 34988943 DOI: 10.1007/7651_2021_453Associated cell lines:
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Hanrath AT, Hatton CF, Gothe F, Browne C, Vowles J, Leary P, Cockell SJ, Cowley SA, James WS, Hambleton S, Duncan CJA
Type I interferon receptor (IFNAR2) deficiency reveals Zika virus cytopathicity in human macrophages and microglia
Hanrath AT et al. Type I interferon receptor (IFNAR2) deficiency reveals Zika virus cytopathicity in human macrophages and microglia. . 2022-00-00. Pubmed ID: 36439115; DOI: 10.3389/fimmu.2022.1035532; PMC: PMC9691778 STBCi044-ASTBCi063-A 2022-00-00 2022-00-00 PubMed: 36439115 DOI: 10.3389/fimmu.2022.1035532Associated cell lines:
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Koh H, Kwon SY, Zhen X, Ha HY, Lee JH
Generation of induced pluripotent stem cell line (KRIBBi004-A) from adult bone marrow CD34(+) cells from a patient carrying 46,XX,t(1;5)(p31.1;35.1) karyotype
Koh H et al. Generation of induced pluripotent stem cell line (KRIBBi004-A) from adult bone marrow CD34(+) cells from a patient carrying 46,XX,t(1;5)(p31.1;35.1) karyotype. . 2021-12-00. Pubmed ID: 34736040; DOI: 10.1016/j.scr.2021.102587 KRIBBi001-AKRIBBi004-A 2021-12-00 2021-12-00 PubMed: 34736040 DOI: 10.1016/j.scr.2021.102587Associated cell lines:
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Li S, Wang Y, Sun H, Wang Z, Zhang Q, Wang Y, Yang J, Shi C, Yuan Y, Wang H, Fan L, Li Z, Xu Y
Construction of induced pluripotent stem cell line (ZZUi031-A) of a healthy young Chinese Han male
Li S et al. Construction of induced pluripotent stem cell line (ZZUi031-A) of a healthy young Chinese Han male. . 2021-12-00. Pubmed ID: 34856467; DOI: 10.1016/j.scr.2021.102608 ZZUi031-A 2021-12-00 2021-12-00 PubMed: 34856467 DOI: 10.1016/j.scr.2021.102608Associated cell lines:
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Mehta A, Lu P, Taylor BV, Charlesworth J, Cook AL, Burdon KP, Hewitt AW, Young KM
Generation of MNZTASi001-A, a human pluripotent stem cell line from a person with primary progressive multiple sclerosis
Mehta A et al. Generation of MNZTASi001-A, a human pluripotent stem cell line from a person with primary progressive multiple sclerosis. . 2021-12-00. Pubmed ID: 34678664; DOI: 10.1016/j.scr.2021.102568 MNZTASi001-A 2021-12-00 2021-12-00 PubMed: 34678664 DOI: 10.1016/j.scr.2021.102568Associated cell lines:
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Ferrari Daniela, D'Anzi Angela, Casamassa Alessia, Bernardini Laura, Tata Ada Maria, Vescovi Angelo Luigi, Rosati Jessica
Functional outcomes of copy number variations of Chrna7 gene
Ferrari Daniela et al. Functional outcomes of copy number variations of Chrna7 gene. . 2022-00-00. DOI: 10.1016/b978-0-12-823882-0.00012-6 CSSi005-A 2022-00-00 2022-00-00 DOI: 10.1016/b978-0-12-823882-0.00012-6Associated cell lines:
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Kusena JWT, Shariatzadeh M, Thomas RJ, Wilson SL
Understanding cell culture dynamics: a tool for defining protocol parameters for improved processes and efficient manufacturing using human embryonic stem cells
Kusena JWT et al. Understanding cell culture dynamics: a tool for defining protocol parameters for improved processes and efficient manufacturing using human embryonic stem cells. . 2021-12-00. Pubmed ID: 33757391; DOI: 10.1080/21655979.2021.1902696; PMC: PMC8806349 WAe009-A 2021-12-00 2021-12-00 PubMed: 33757391 DOI: 10.1080/21655979.2021.1902696Associated cell lines:
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Cutts J, Kostes W, Brafman DA
Generation of 3X FLAG-tagged human embryonic stem cell (hESC) line to study WNT-induced β-catenin DNA interactions (HVRDe009-A-2)
Cutts J et al. Generation of 3X FLAG-tagged human embryonic stem cell (hESC) line to study WNT-induced β-catenin DNA interactions (HVRDe009-A-2). . 2021-12-00. Pubmed ID: 34736039; DOI: 10.1016/j.scr.2021.102586 HVRDe009-AHVRDe009-A-2 2021-12-00 2021-12-00 PubMed: 34736039 DOI: 10.1016/j.scr.2021.102586Associated cell lines:
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Halliez C, Ibrahim H, Otonkoski T, Mallone R
In vitro beta-cell killing models using immune cells and human pluripotent stem cell-derived islets: Challenges and opportunities
Halliez C et al. In vitro beta-cell killing models using immune cells and human pluripotent stem cell-derived islets: Challenges and opportunities. . 2022-00-00. Pubmed ID: 36726462; DOI: 10.3389/fendo.2022.1076683; PMC: PMC9885197 SCSe001-ASCSe001-A-3 2022-00-00 2022-00-00 PubMed: 36726462 DOI: 10.3389/fendo.2022.1076683Associated cell lines:
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Jakobi T, Groß J, Cyganek L, Doroudgar S
Transcriptional Effects of Candidate COVID-19 Treatments on Cardiac Myocytes
Jakobi T et al. Transcriptional Effects of Candidate COVID-19 Treatments on Cardiac Myocytes. . 2022-00-00. Pubmed ID: 35686037; DOI: 10.3389/fcvm.2022.844441; PMC: PMC9170897 UMGi014-C 2022-00-00 2022-00-00 PubMed: 35686037 DOI: 10.3389/fcvm.2022.844441Associated cell lines:
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Lindner M, Laporte A, Elomaa L, Lee-Thedieck C, Olmer R, Weinhart M
Flow-induced glycocalyx formation and cell alignment of HUVECs compared to iPSC-derived ECs for tissue engineering applications
Lindner M et al. Flow-induced glycocalyx formation and cell alignment of HUVECs compared to iPSC-derived ECs for tissue engineering applications. . 2022-00-00. Pubmed ID: 36133919; DOI: 10.3389/fcell.2022.953062; PMC: PMC9483120 MHHi001-A 2022-00-00 2022-00-00 PubMed: 36133919 DOI: 10.3389/fcell.2022.953062Associated cell lines:
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Wang B, Zhu S, Deng Y, Sai X, Chen Z, Liu J, Li G, Liu N, Chen J, Yu C, Sun T, Zhu P
Establishment of a CRISPR/Cas9-mediated GATAD2B homozygous knockout human embryonic stem cell line
Wang B et al. Establishment of a CRISPR/Cas9-mediated GATAD2B homozygous knockout human embryonic stem cell line. . 2021-12-00. Pubmed ID: 34749018; DOI: 10.1016/j.scr.2021.102590 WAe001-A-73WAe001-A-74 2021-12-00 2021-12-00 PubMed: 34749018 DOI: 10.1016/j.scr.2021.102590Associated cell lines:
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Eintracht J, Harding P, Lima Cunha D, Moosajee M
Efficient embryoid-based method to improve generation of optic vesicles from human induced pluripotent stem cells
Eintracht J et al. Efficient embryoid-based method to improve generation of optic vesicles from human induced pluripotent stem cells. . 2022-00-00. Pubmed ID: 35811797; DOI: 10.12688/f1000research.108829.1; PMC: PMC9218590 UCLi016-AUCLi017-A 2022-00-00 2022-00-00 PubMed: 35811797 DOI: 10.12688/f1000research.108829.1 -
Cui H, Jin X, Yang QH, Qu LH, Hou BK, Li ZH, Huang HB
Various phenotypes of autosomal dominant cone-rod dystrophy with cone-rod homeobox mutation in two Chinese families
Cui H et al. Various phenotypes of autosomal dominant cone-rod dystrophy with cone-rod homeobox mutation in two Chinese families. . 2022-00-00. Pubmed ID: 36536961; DOI: 10.18240/ijo.2022.12.04; PMC: PMC9729094 INMi003-A 2022-00-00 2022-00-00 PubMed: 36536961 DOI: 10.18240/ijo.2022.12.04Associated cell lines:
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Ray A, Joshi JM, Sundaravadivelu PK, Raina K, Lenka N, Kaveeshwar V, Thummer RP
An Overview on Promising Somatic Cell Sources Utilized for the Efficient Generation of Induced Pluripotent Stem Cells
Ray A et al. An Overview on Promising Somatic Cell Sources Utilized for the Efficient Generation of Induced Pluripotent Stem Cells. . 2021-12-00. Pubmed ID: 34100193; DOI: 10.1007/s12015-021-10200-3 MUSIi006-AMUSIi007-AKCLi002-ACSi001-AIPTi001-AGENYOi004-AIGIBi001-AREGUi003-AGIBHi001-AGENYOi005-ASDQLCHi007-ASDQLCHi014-AICGi014-ACSUXHi002-ASMBCi006-AGWCMCi001-ASDQLCHi033-APUMCHi006-AIGIBi002-A 2021-12-00 2021-12-00 PubMed: 34100193 DOI: 10.1007/s12015-021-10200-3 -
Zhao SR, Shen M, Lee C, Zha Y, Guevara JV, Wheeler MT, Wu JC
Generation of three induced pluripotent stem cell lines from hypertrophic cardiomyopathy patients carrying TNNI3 mutations
Zhao SR et al. Generation of three induced pluripotent stem cell lines from hypertrophic cardiomyopathy patients carrying TNNI3 mutations. . 2021-12-00. Pubmed ID: 34798544; DOI: 10.1016/j.scr.2021.102597; PMC: PMC9095754 SCVIi017-ASCVIi018-ASCVIi019-A 2021-12-00 2021-12-00 PubMed: 34798544 DOI: 10.1016/j.scr.2021.102597Associated cell lines:
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Chen H, Zhang M, Zhang J, Chen Y, Zuo Y, Xie Z, Zhou G, Chen S, Chen Y
Application of Induced Pluripotent Stem Cell-Derived Models for Investigating microRNA Regulation in Developmental Processes
Chen H et al. Application of Induced Pluripotent Stem Cell-Derived Models for Investigating microRNA Regulation in Developmental Processes. . 2022-00-00. Pubmed ID: 35719367; DOI: 10.3389/fgene.2022.899831; PMC: PMC9204592 GZHMCi008-A 2022-00-00 2022-00-00 PubMed: 35719367 DOI: 10.3389/fgene.2022.899831Associated cell lines:
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Fluhr TL, Tabatabaeifar M, Syring H, Göhring G, Schaefer F, Jung-Klawitter S
Generation of an induced pluripotent stem cell line (DHMCi006-A) from a patient with autosomal recessive polycystic kidney disease (ARPKD) carrying a compound heterozygous missense mutation in the fibrocystin encoding PKHD1 gene
Fluhr TL et al. Generation of an induced pluripotent stem cell line (DHMCi006-A) from a patient with autosomal recessive polycystic kidney disease (ARPKD) carrying a compound heterozygous missense mutation in the fibrocystin encoding PKHD1 gene. . 2021-12-00. Pubmed ID: 34695767; DOI: 10.1016/j.scr.2021.102579 DHMCi006-A 2021-12-00 2021-12-00 PubMed: 34695767 DOI: 10.1016/j.scr.2021.102579Associated cell lines:
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Meshrkey F, Cabrera Ayuso A, Rao RR, Iyer S
Quantitative analysis of mitochondrial morphologies in human induced pluripotent stem cells for Leigh syndrome
Meshrkey F et al. Quantitative analysis of mitochondrial morphologies in human induced pluripotent stem cells for Leigh syndrome. . 2021-12-00. Pubmed ID: 34662843; DOI: 10.1016/j.scr.2021.102572; PMC: PMC10332439 UOMi001-AUOMi002-A 2021-12-00 2021-12-00 PubMed: 34662843 DOI: 10.1016/j.scr.2021.102572 -
Tabatabaeifar M, Fluhr TL, Syring H, Göhring G, Schaefer F, Jung-Klawitter S
Generation of an induced pluripotent stem cell line (DHMCi007-A) from a patient with autosomal recessive polycystic kidney disease (ARPKD) carrying a homozygous missense mutation in the fibrocystin-encoding PKHD1 gene
Tabatabaeifar M et al. Generation of an induced pluripotent stem cell line (DHMCi007-A) from a patient with autosomal recessive polycystic kidney disease (ARPKD) carrying a homozygous missense mutation in the fibrocystin-encoding PKHD1 gene. . 2021-12-00. Pubmed ID: 34688127; DOI: 10.1016/j.scr.2021.102573 DHMCi007-A 2021-12-00 2021-12-00 PubMed: 34688127 DOI: 10.1016/j.scr.2021.102573Associated cell lines:
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Sundaravadivelu PK, Raina K, Thool M, Ray A, Joshi JM, Kaveeshwar V, Sudhagar S, Lenka N, Thummer RP
Tissue-Restricted Stem Cells as Starting Cell Source for Efficient Generation of Pluripotent Stem Cells: An Overview
Sundaravadivelu PK et al. Tissue-Restricted Stem Cells as Starting Cell Source for Efficient Generation of Pluripotent Stem Cells: An Overview. . 2022-00-00. Pubmed ID: 34611861; DOI: 10.1007/5584_2021_660 JUCTCi014-AJUCTCi015-AJUCTCi016-AGZHMCi005-A 2022-00-00 2022-00-00 PubMed: 34611861 DOI: 10.1007/5584_2021_660Associated cell lines:
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Ma X, Zhu L, Chen W, Sheng M, Peng F, Liang M, Zhao Y, Wang Y, Feng Z
Generation of an iPSC line (SMCPGi001-A) from a patient with Bain type X-linked mental retardation syndrome carrying HNRNPH2 gene mutation
Ma X et al. Generation of an iPSC line (SMCPGi001-A) from a patient with Bain type X-linked mental retardation syndrome carrying HNRNPH2 gene mutation. . 2021-12-00. Pubmed ID: 34763229; DOI: 10.1016/j.scr.2021.102571 SMCPGHi001-A 2021-12-00 2021-12-00 PubMed: 34763229 DOI: 10.1016/j.scr.2021.102571Associated cell lines:
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Matakovic L, Overeem AW, Klappe K, van IJzendoorn SCD
Induction of Bile Canaliculi-Forming Hepatocytes from Human Pluripotent Stem Cells
Matakovic L et al. Induction of Bile Canaliculi-Forming Hepatocytes from Human Pluripotent Stem Cells. . 2022-00-00. Pubmed ID: 36125710; DOI: 10.1007/978-1-0716-2557-6_4 BRCi009-A 2022-00-00 2022-00-00 PubMed: 36125710 DOI: 10.1007/978-1-0716-2557-6_4Associated cell lines:
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Suwanpitak S, Promnakhon N, Netsrithong R, Wattanapanitch M
Efficient Generation of iPSC-Derived Hematoendothelial Progenitors and Specification Toward T cell Lineage
Suwanpitak S et al. Efficient Generation of iPSC-Derived Hematoendothelial Progenitors and Specification Toward T cell Lineage. . 2022-00-00. Pubmed ID: 33755900; DOI: 10.1007/7651_2021_355 MUSIi011-AMUSIi011-B 2022-00-00 2022-00-00 PubMed: 33755900 DOI: 10.1007/7651_2021_355Associated cell lines:
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Belbachir N, Lai C, Rhee JW, Zhuge Y, Perez MV, Sallam K, Wu JC
Generation of two induced pluripotent stem cell lines from Brugada syndrome affected patients carrying SCN5A mutations
Belbachir N et al. Generation of two induced pluripotent stem cell lines from Brugada syndrome affected patients carrying SCN5A mutations. . 2021-12-00. Pubmed ID: 34856468; DOI: 10.1016/j.scr.2021.102605 SCVIi026-ASCVIi027-A 2021-12-00 2021-12-00 PubMed: 34856468 DOI: 10.1016/j.scr.2021.102605Associated cell lines:
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Thongsin N, Wattanapanitch M
CRISPR/Cas9 Ribonucleoprotein Complex-Mediated Efficient B2M Knockout in Human Induced Pluripotent Stem Cells (iPSCs)
Thongsin N et al. CRISPR/Cas9 Ribonucleoprotein Complex-Mediated Efficient B2M Knockout in Human Induced Pluripotent Stem Cells (iPSCs). . 2022-00-00. Pubmed ID: 33945142; DOI: 10.1007/7651_2021_352 MUSIi001-A 2022-00-00 2022-00-00 PubMed: 33945142 DOI: 10.1007/7651_2021_352Associated cell lines:
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Valadez-Barba V., Cota-Coronado A., Barragán-Álvarez C.P., Padilla-Camberos E., Díaz-Martínez N.E.
iPSC for modeling of metabolic and neurodegenerative disorders
Valadez-Barba V. et al. iPSC for modeling of metabolic and neurodegenerative disorders. . 2022-00-00. DOI: 10.1016/b978-0-12-823882-0.00007-2 IPTi005-AIPTi007-A 2022-00-00 2022-00-00 DOI: 10.1016/b978-0-12-823882-0.00007-2 -
Chang S, Hur SK, Naveh NSS, Thorvaldsen JL, French DL, Gagne AL, Jobaliya CD, Anguera MC, Bartolomei MS, Kalish JM
Derivation and investigation of the first human cell-based model of Beckwith-Wiedemann syndrome
Chang S et al. Derivation and investigation of the first human cell-based model of Beckwith-Wiedemann syndrome. . 2021-12-00. Pubmed ID: 33300436; DOI: 10.1080/15592294.2020.1861172; PMC: PMC8813081 KSCBi007-A 2021-12-00 2021-12-00 PubMed: 33300436 DOI: 10.1080/15592294.2020.1861172Associated cell lines:
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Tayanloo-Beik Akram, Nikkhah Amirabbas, Roudsari Peyvand Parhizkar, Aghayan Hamidreza, Rezaei-Tavirani Mostafa, Nasli-Esfahani Ensieh, Mafi Ahmad Rezazadeh, Nikandish Mohsen, Shouroki Fatemeh Fazeli, Arjmand Babak, Larijani Bagher
Application of Biocompatible Scaffolds in Stem-Cell-Based Dental Tissue Engineering
Tayanloo-Beik Akram et al. Application of Biocompatible Scaffolds in Stem-Cell-Based Dental Tissue Engineering. . 2022-00-00. DOI: 10.1007/5584_2022_734 FMCPGHi001-A 2022-00-00 2022-00-00 DOI: 10.1007/5584_2022_734Associated cell lines:
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Huang C, Ai X, Hu L, Ren D
The Role of NMP22 and CSTB Levels in Predicting Postoperative Recurrence of Bladder Cancer
Huang C et al. The Role of NMP22 and CSTB Levels in Predicting Postoperative Recurrence of Bladder Cancer. . 2022-00-00. Pubmed ID: 35647202; DOI: 10.1155/2022/6735310; PMC: PMC9135568 UNIMGi003-AUNIMGi004-A 2022-00-00 2022-00-00 PubMed: 35647202 DOI: 10.1155/2022/6735310Associated cell lines:
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Luo Y, Zhu D, Fang JH
Editorial: Gene regulation mediated by competing RNA: From benchside to bedside
Luo Y et al. Editorial: Gene regulation mediated by competing RNA: From benchside to bedside. . 2022-00-00. Pubmed ID: 36506324; DOI: 10.3389/fgene.2022.1085155; PMC: PMC9727387 GZHMCi008-A 2022-00-00 2022-00-00 PubMed: 36506324 DOI: 10.3389/fgene.2022.1085155Associated cell lines:
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Cao S, Ma J, Zhang J, Guo R, Liu X, Li M
Reprogramming of one human induced pluripotent stem cell line from healthy donor
Cao S et al. Reprogramming of one human induced pluripotent stem cell line from healthy donor. . 2021-12-00. Pubmed ID: 34871962; DOI: 10.1016/j.scr.2021.102613 HEBHMUi001-ASIAISi011-ARCPCMi008-AHEBHMUi010-A 2021-12-00 2021-12-00 PubMed: 34871962 DOI: 10.1016/j.scr.2021.102613Associated cell lines:
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Carcamo-Orive Ivan
iPSCs in insulin resistance, type 2 diabetes, and the metabolic syndrome
Carcamo-Orive Ivan. iPSCs in insulin resistance, type 2 diabetes, and the metabolic syndrome. . 2022-00-00. DOI: 10.1016/b978-0-323-99892-5.00020-7 PUMCHi001-APUMCHi001-A-1 2022-00-00 2022-00-00 DOI: 10.1016/b978-0-323-99892-5.00020-7Associated cell lines:
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Miranda CC, Akenhead ML, Silva TP, Derr MA, Vemuri MC, Cabral JMS, Fernandes TG
A Dynamic 3D Aggregate-Based System for the Successful Expansion and Neural Induction of Human Pluripotent Stem Cells
Miranda CC et al. A Dynamic 3D Aggregate-Based System for the Successful Expansion and Neural Induction of Human Pluripotent Stem Cells. . 2022-00-00. Pubmed ID: 35308123; DOI: 10.3389/fncel.2022.838217; PMC: PMC8928726 SDUKIi002-ASDUKIi006-A 2022-00-00 2022-00-00 PubMed: 35308123 DOI: 10.3389/fncel.2022.838217Associated cell lines:
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Song Y, Zheng Z, Lian J
Deciphering Common Long QT Syndrome Using CRISPR/Cas9 in Human-Induced Pluripotent Stem Cell-Derived Cardiomyocytes
Song Y et al. Deciphering Common Long QT Syndrome Using CRISPR/Cas9 in Human-Induced Pluripotent Stem Cell-Derived Cardiomyocytes. . 2022-00-00. Pubmed ID: 35647048; DOI: 10.3389/fcvm.2022.889519; PMC: PMC9136094 PSMi003-APSMi006-ANUIGi003-ANUIGi004-ANUIGi005-ANUIGi005-BNUIGi005-CNUIGi006-ANUIGi006-BNUIGi006-CNUIGi007-ANUIGi007-BNUIGi012-AKSCBi014-AKSCBi015-ANCUFi001-AXACHi015-A 2022-00-00 2022-00-00 PubMed: 35647048 DOI: 10.3389/fcvm.2022.889519 -
Novak G, Finkbeiner S, Skibinski G, Skupin A
Generation of two human induced pluripotent stem cell lines (iPSCs) with mutations of the α-synuclein (SNCA) gene associated with Parkinson's disease; the A53T mutation (LCSBi003) and a triplication of the SNCA gene (LCSBi007)
Novak G et al. Generation of two human induced pluripotent stem cell lines (iPSCs) with mutations of the α-synuclein (SNCA) gene associated with Parkinson's disease; the A53T mutation (LCSBi003) and a triplication of the SNCA gene (LCSBi007). . 2021-12-00. Pubmed ID: 34826737; DOI: 10.1016/j.scr.2021.102600; PMC: PMC9124237 LCSBi003-ALCSBi003-BLCSBi003-CLCSBi007-ALCSBi007-B 2021-12-00 2021-12-00 PubMed: 34826737 DOI: 10.1016/j.scr.2021.102600Associated cell lines:
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Han HJ, Kim JH
Generation of a TLR2 knockout human induced pluripotent stem cell line using CRISPR/Cas9
Han HJ et al. Generation of a TLR2 knockout human induced pluripotent stem cell line using CRISPR/Cas9. . 2021-12-00. Pubmed ID: 34710836; DOI: 10.1016/j.scr.2021.102578 KSCBi005-AKSCBi005-A-5KSCBi005-A-7 2021-12-00 2021-12-00 PubMed: 34710836 DOI: 10.1016/j.scr.2021.102578Associated cell lines:
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Rapedius M, Obergrussberger A, Humphries ESA, Scholz S, Rinke-Weiss I, Goetze TA, Brinkwirth N, Rotordam MG, Strassmaier T, Randolph A, Friis S, Liutkute A, Seibertz F, Voigt N, Fertig N
There is no F in APC: Using physiological fluoride-free solutions for high throughput automated patch clamp experiments
Rapedius M et al. There is no F in APC: Using physiological fluoride-free solutions for high throughput automated patch clamp experiments. . 2022-00-00. Pubmed ID: 36072300; DOI: 10.3389/fnmol.2022.982316; PMC: PMC9443850 UMGi014-CUMGi014-C-14 2022-00-00 2022-00-00 PubMed: 36072300 DOI: 10.3389/fnmol.2022.982316Associated cell lines:
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Novak G, Finkbeiner S, Skibinski G, Skupin A
Generation of two human induced pluripotent stem cell lines from fibroblasts of unrelated Parkinson's patients carrying the G2019S mutation in the LRRK2 gene (LCSBi005, LCSBi006)
Novak G et al. Generation of two human induced pluripotent stem cell lines from fibroblasts of unrelated Parkinson's patients carrying the G2019S mutation in the LRRK2 gene (LCSBi005, LCSBi006). . 2021-12-00. Pubmed ID: 34736041; DOI: 10.1016/j.scr.2021.102569 LCSBi002-BLCSBi004-ALCSBi004-BLCSBi005-ALCSBi005-BLCSBi006-A 2021-12-00 2021-12-00 PubMed: 34736041 DOI: 10.1016/j.scr.2021.102569Associated cell lines:
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Giovenale AMG, Ruotolo G, Soriano AA, Turco EM, Rotundo G, Casamassa A, D'Anzi A, Vescovi AL, Rosati J
Deepening the understanding of CNVs on chromosome 15q11-13 by using hiPSCs: An overview
Giovenale AMG et al. Deepening the understanding of CNVs on chromosome 15q11-13 by using hiPSCs: An overview. . 2022-00-00. Pubmed ID: 36684422; DOI: 10.3389/fcell.2022.1107881; PMC: PMC9852989 BIONi010-ABIONi010-BBIONi010-C 2022-00-00 2022-00-00 PubMed: 36684422 DOI: 10.3389/fcell.2022.1107881Associated cell lines:
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Amaral Olga, Duarte Ana, Ribeiro Diogo, Santos Renato, Bragança José
Applications of iPSCs in Gaucher Disease and other rare sphingolipidoses
Amaral Olga et al. Applications of iPSCs in Gaucher Disease and other rare sphingolipidoses. . 2022-00-00. DOI: 10.1016/b978-0-323-85767-3.00001-3 INSAi001-A 2022-00-00 2022-00-00 DOI: 10.1016/b978-0-323-85767-3.00001-3Associated cell lines:
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Gerull B, Brodehl A
Insights Into Genetics and Pathophysiology of Arrhythmogenic Cardiomyopathy
Gerull B et al. Insights Into Genetics and Pathophysiology of Arrhythmogenic Cardiomyopathy. . 2021-12-00. Pubmed ID: 34478111; DOI: 10.1007/s11897-021-00532-z; PMC: PMC8616880 HDZi001-A 2021-12-00 2021-12-00 PubMed: 34478111 DOI: 10.1007/s11897-021-00532-zAssociated cell lines:
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Wu J, Tian W, Zhan F, Luan X, Cao L
Generation of an human induced pluripotent stem cell JTUi007-A from a patient with CSF1R-related leukoencephalopathy carrying heterozygous p.Ile794Thr mutation in CSF1R gene
Wu J et al. Generation of an human induced pluripotent stem cell JTUi007-A from a patient with CSF1R-related leukoencephalopathy carrying heterozygous p.Ile794Thr mutation in CSF1R gene. . 2021-12-00. Pubmed ID: 34837774; DOI: 10.1016/j.scr.2021.102593 JTUi007-A 2021-12-00 2021-12-00 PubMed: 34837774 DOI: 10.1016/j.scr.2021.102593Associated cell lines:
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Grimm E, van der Hoeven F, Sardella D, Willig KI, Engel U, Veits N, Engel R, Cavalcanti-Adam EA, Bestvater F, Bordoni L, Jennemann R, Schönig K, Schiessl IM, Sandhoff R
A Clathrin light chain A reporter mouse for in vivo imaging of endocytosis
Grimm E et al. A Clathrin light chain A reporter mouse for in vivo imaging of endocytosis. . 2022-00-00. Pubmed ID: 36149863; DOI: 10.1371/journal.pone.0273660; PMC: PMC9506643 CRMi001-ACRMi001-A-1 2022-00-00 2022-00-00 PubMed: 36149863 DOI: 10.1371/journal.pone.0273660Associated cell lines:
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Chen J, Song Y, Gu J, Chen L
Reprogramming of a human induced pluripotent stem cell line from a long QT syndrome patient harboring a heterozygous mutation of c.1537C > T in SCN5A gene
Chen J et al. Reprogramming of a human induced pluripotent stem cell line from a long QT syndrome patient harboring a heterozygous mutation of c.1537C > T in SCN5A gene. . 2021-12-00. Pubmed ID: 34678660; DOI: 10.1016/j.scr.2021.102576 ZJYYPHi001-A 2021-12-00 2021-12-00 PubMed: 34678660 DOI: 10.1016/j.scr.2021.102576Associated cell lines:
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Dai Q, Jiang W, Huang F, Song F, Zhang J, Zhao H
Recent Advances in Liver Engineering With Decellularized Scaffold
Dai Q et al. Recent Advances in Liver Engineering With Decellularized Scaffold. . 2022-00-00. Pubmed ID: 35223793; DOI: 10.3389/fbioe.2022.831477; PMC: PMC8866951 UUMCBi001-AUUMCBi002-A 2022-00-00 2022-00-00 PubMed: 35223793 DOI: 10.3389/fbioe.2022.831477Associated cell lines:
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Bourque Kyla, Mnasri Nourhen, Jones-Tabah Jace, Martins-Cannavino Kimberly, Hébert Terence E.
Drug Discovery in Induced Pluripotent Stem Cell Models
Bourque Kyla et al. Drug Discovery in Induced Pluripotent Stem Cell Models. . 2022-00-00. DOI: 10.1016/b978-0-12-820472-6.00049-9 LUMCi027-AICGi019-AICGi019-B 2022-00-00 2022-00-00 DOI: 10.1016/b978-0-12-820472-6.00049-9Associated cell lines:
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Zhigalina DI, Malakhova AA, Vasilyeva OY, Grigor'eva EV, Sivtsev AA, Kolesnikov NA, Lopatkina ME, Savchenko RR, Zhalsanova IZ, Postrigan' AE, Zarubin AA, Nikitina TV, Bueverov AO, Bogomolov PO, Zakian SM, Skryabin NA
Generation of an induced pluripotent stem cell line ICGi030-A from a Wilson's disease patient carrying a frameshift mutation p.Lys1013fs and missense mutation p.H1069Q in the ATP7B gene
Zhigalina DI et al. Generation of an induced pluripotent stem cell line ICGi030-A from a Wilson's disease patient carrying a frameshift mutation p.Lys1013fs and missense mutation p.H1069Q in the ATP7B gene. . 2021-12-00. Pubmed ID: 34736038; DOI: 10.1016/j.scr.2021.102556 ICGi030-A 2021-12-00 2021-12-00 PubMed: 34736038 DOI: 10.1016/j.scr.2021.102556Associated cell lines:
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Zhou H, Wu Z, Wang Y, Wu Q, Hu M, Ma S, Zhou M, Sun Y, Yu B, Ye J, Jiang W, Fu Z, Gong Y
Rare Diseases in Glycosphingolipid Metabolism
Zhou H et al. Rare Diseases in Glycosphingolipid Metabolism. . 2022-00-00. Pubmed ID: 35503182; DOI: 10.1007/978-981-19-0394-6_13 TRNDi009-C 2022-00-00 2022-00-00 PubMed: 35503182 DOI: 10.1007/978-981-19-0394-6_13Associated cell lines:
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Mao Z, Li Y, Huang L, Chen Y, Luo H, Zhang S, Chen H
Generation of an induced pluripotent stem cell line HUSTTJi001-A from a Moyamoya disease patient with RNF213 gene mutation
Mao Z et al. Generation of an induced pluripotent stem cell line HUSTTJi001-A from a Moyamoya disease patient with RNF213 gene mutation. . 2021-12-00. Pubmed ID: 34749017; DOI: 10.1016/j.scr.2021.102575 HUSTTJi001-A 2021-12-00 2021-12-00 PubMed: 34749017 DOI: 10.1016/j.scr.2021.102575Associated cell lines:
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Luo Y, Chen Y, Zhang M, Ma X, Zhu D, Chen Y
Generation of an induced pluripotent stem cell line GZHMCi008-A derived from a patient with SRY-positive 46,XX testicular disorder of sex development
Luo Y et al. Generation of an induced pluripotent stem cell line GZHMCi008-A derived from a patient with SRY-positive 46,XX testicular disorder of sex development. . 2021-12-00. Pubmed ID: 34710837; DOI: 10.1016/j.scr.2021.102583 GZHMCi008-A 2021-12-00 2021-12-00 PubMed: 34710837 DOI: 10.1016/j.scr.2021.102583Associated cell lines:
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Mao Y, Zhang T
Knockdown of SHMT2 enhances the sensitivity of gastric cancer cells to radiotherapy through the Wnt/β-catenin pathway
Mao Y et al. Knockdown of SHMT2 enhances the sensitivity of gastric cancer cells to radiotherapy through the Wnt/β-catenin pathway. . 2022-00-00. Pubmed ID: 36213384; DOI: 10.1515/biol-2022-0480; PMC: PMC9490860 WAe009-AWAe009-A-67 2022-00-00 2022-00-00 PubMed: 36213384 DOI: 10.1515/biol-2022-0480Associated cell lines:
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Rao L, Gennerich A
Single-Molecule Studies on the Motion and Force Generation of the Kinesin-3 Motor KIF1A
Rao L et al. Single-Molecule Studies on the Motion and Force Generation of the Kinesin-3 Motor KIF1A. . 2022-00-00. Pubmed ID: 36063335; DOI: 10.1007/978-1-0716-2229-2_21; PMC: PMC9609470 SDUBMSi001-A 2022-00-00 2022-00-00 PubMed: 36063335 DOI: 10.1007/978-1-0716-2229-2_21Associated cell lines:
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Su T, Liang L, Zhang L, Wang J, Chen L, Su C, Cao J, Yu Q, Deng S, Chan HF, Tang S, Guo Y, Chen J
Retinal organoids and microfluidic chip-based approaches to explore the retinitis pigmentosa with USH2A mutations
Su T et al. Retinal organoids and microfluidic chip-based approaches to explore the retinitis pigmentosa with USH2A mutations. . 2022-00-00. Pubmed ID: 36185441; DOI: 10.3389/fbioe.2022.939774; PMC: PMC9524156 KLRMMEi001-AKLRMMEi002-A 2022-00-00 2022-00-00 PubMed: 36185441 DOI: 10.3389/fbioe.2022.939774Associated cell lines:
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Bharucha N, Ataam JA, Gavidia AA, Karakikes I
Generation of AAVS1 integrated doxycycline-inducible CRISPR-Prime Editor human induced pluripotent stem cell line
Bharucha N et al. Generation of AAVS1 integrated doxycycline-inducible CRISPR-Prime Editor human induced pluripotent stem cell line. . 2021-12-00. Pubmed ID: 34875545; DOI: 10.1016/j.scr.2021.102610; PMC: PMC9126997 SCVIi028-ASCVIi028-A-1 2021-12-00 2021-12-00 PubMed: 34875545 DOI: 10.1016/j.scr.2021.102610Associated cell lines:
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Nakashima Y, Yoshida S, Tsukahara M
Semi-3D cultures using Laminin 221 as a coating material for human induced pluripotent stem cells
Nakashima Y et al. Semi-3D cultures using Laminin 221 as a coating material for human induced pluripotent stem cells. . 2022-00-00. Pubmed ID: 36176714; DOI: 10.1093/rb/rbac060; PMC: PMC9514851 RCe013-A 2022-00-00 2022-00-00 PubMed: 36176714 DOI: 10.1093/rb/rbac060Associated cell lines:
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Siehler J, Blöchinger AK, Meier M, Lickert H
Engineering islets from stem cells for advanced therapies of diabetes
Siehler J et al. Engineering islets from stem cells for advanced therapies of diabetes. . 2021-12-00. Pubmed ID: 34376833; DOI: 10.1038/s41573-021-00262-w HMGUi001-AHMGUi001-A-4HMGUi001-A-8 2021-12-00 2021-12-00 PubMed: 34376833 DOI: 10.1038/s41573-021-00262-wAssociated cell lines:
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Ma J, Ni K, Cai W, Li B, Qian Q, Sun D
Generation of an induced pluripotent stem cell line ATCi001-A from a three-year-old Chinese girl with Brown-Vialetto-Van Laere syndrome-2
Ma J et al. Generation of an induced pluripotent stem cell line ATCi001-A from a three-year-old Chinese girl with Brown-Vialetto-Van Laere syndrome-2. . 2021-12-00. Pubmed ID: 34736036; DOI: 10.1016/j.scr.2021.102589 ATCi001-A 2021-12-00 2021-12-00 PubMed: 34736036 DOI: 10.1016/j.scr.2021.102589Associated cell lines:
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Kleschevnikov AM
Enhanced GIRK2 channel signaling in Down syndrome: A feasible role in the development of abnormal nascent neural circuits
Kleschevnikov AM. Enhanced GIRK2 channel signaling in Down syndrome: A feasible role in the development of abnormal nascent neural circuits. . 2022-00-00. Pubmed ID: 36171878; DOI: 10.3389/fgene.2022.1006068; PMC: PMC9510977 NSi001-ANSi001-BNSi001-C 2022-00-00 2022-00-00 PubMed: 36171878 DOI: 10.3389/fgene.2022.1006068 -
Andrysiak K, Martyniak A, Potulska-Chromik A, Kostera-Pruszczyk A, Stępniewski J, Dulak J
Generation of DMBi002-A human induced pluripotent stem cell line from patient with Spinal muscular atrophy type 3
Andrysiak K et al. Generation of DMBi002-A human induced pluripotent stem cell line from patient with Spinal muscular atrophy type 3. . 2021-12-00. Pubmed ID: 34678665; DOI: 10.1016/j.scr.2021.102563 DMBi002-A 2021-12-00 2021-12-00 PubMed: 34678665 DOI: 10.1016/j.scr.2021.102563Associated cell lines:
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Fang J, Zhang P, Zhou Y, Chiang CW, Tan J, Hou Y, Stauffer S, Li L, Pieper AA, Cummings J, Cheng F
Endophenotype-based in silico network medicine discovery combined with insurance record data mining identifies sildenafil as a candidate drug for Alzheimer's disease
Fang J et al. Endophenotype-based in silico network medicine discovery combined with insurance record data mining identifies sildenafil as a candidate drug for Alzheimer's disease. . 2021-12-00. Pubmed ID: 35572351; DOI: 10.1038/s43587-021-00138-z; PMC: PMC9097949 HVRDi001-A-1 2021-12-00 2021-12-00 PubMed: 35572351 DOI: 10.1038/s43587-021-00138-zAssociated cell lines:
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Bergmann T, Liu Y, Skov J, Mogus L, Lee J, Pfisterer U, Handfield LF, Asenjo-Martinez A, Lisa-Vargas I, Seemann SE, Lee JTH, Patikas N, Kornum BR, Denham M, Hyttel P, Witter MP, Gorodkin J, Pers TH, Hemberg M, Khodosevich K, Hall VJ
Production of human entorhinal stellate cell-like cells by forward programming shows an important role of Foxp1 in reprogramming
Bergmann T et al. Production of human entorhinal stellate cell-like cells by forward programming shows an important role of Foxp1 in reprogramming. . 2022-00-00. Pubmed ID: 36046338; DOI: 10.3389/fcell.2022.976549; PMC: PMC9420913 STBCi064-A 2022-00-00 2022-00-00 PubMed: 36046338 DOI: 10.3389/fcell.2022.976549Associated cell lines:
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Li X, Wei W, Li X, Qi L, Lu S, Wei H, Liu Y, Dong J, Zhang C, Lin T
A heterozygous TTN (c. 79,684C>T) mutant human induced pluripotent stem cell line (ZZUNEUi023-A) generated from a Kazakh patient with dilated cardiomyopathy
Li X et al. A heterozygous TTN (c. 79,684C>T) mutant human induced pluripotent stem cell line (ZZUNEUi023-A) generated from a Kazakh patient with dilated cardiomyopathy. . 2021-12-00. Pubmed ID: 34883393; DOI: 10.1016/j.scr.2021.102614 ZZUNEUi023-A 2021-12-00 2021-12-00 PubMed: 34883393 DOI: 10.1016/j.scr.2021.102614Associated cell lines:
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GÜLER KARA Hale, KOSOVA Buket, DOĞAN Eda, BOZOK ÇETİNTAŞ Vildan, ŞENTÜRK Şerif
CRISPR-Cas Functional Genetic Screening: Traditional Review
GÜLER KARA Hale et al. CRISPR-Cas Functional Genetic Screening: Traditional Review. . 2022-00-00. DOI: 10.5336/medsci.2022-88507 JMUi001-AJMUi001-A-2JMUi001-A-3 2022-00-00 2022-00-00 DOI: 10.5336/medsci.2022-88507Associated cell lines:
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Ercan-Sencicek A. Gulhan, Chennappan Saravanakkumar, Aromalaran Kelly, Kontaridis Maria Irene
Induced pluripotent stem cells for modeling Noonan, Noonan Syndrome with Multiple Lentigines, and Costello Syndromes
Ercan-Sencicek A. Gulhan et al. Induced pluripotent stem cells for modeling Noonan, Noonan Syndrome with Multiple Lentigines, and Costello Syndromes. . 2022-00-00. DOI: 10.1016/b978-0-323-85765-9.00007-2 TRNDi003-A 2022-00-00 2022-00-00 DOI: 10.1016/b978-0-323-85765-9.00007-2Associated cell lines:
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Wang Y, Xiong W, Zhao S, Li B, Chang ACY
Generation of two induced pluripotent stem cell lines, SHIPMi001-A from a patient with hypertrophic cardiomyopathy caused by MYBPC3 gene mutation and SHIPMi002-A from a healthy male individual
Wang Y et al. Generation of two induced pluripotent stem cell lines, SHIPMi001-A from a patient with hypertrophic cardiomyopathy caused by MYBPC3 gene mutation and SHIPMi002-A from a healthy male individual. . 2021-12-00. Pubmed ID: 34785479; DOI: 10.1016/j.scr.2021.102594 SHIPMi001-ASHIPMi002-A 2021-12-00 2021-12-00 PubMed: 34785479 DOI: 10.1016/j.scr.2021.102594Associated cell lines:
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Sharma V, Nehra S, Do LH, Ghosh A, Deshpande AJ, Singhal N
Biphasic cell cycle defect causes impaired neurogenesis in down syndrome
Sharma V et al. Biphasic cell cycle defect causes impaired neurogenesis in down syndrome. . 2022-00-00. Pubmed ID: 36313423; DOI: 10.3389/fgene.2022.1007519; PMC: PMC9596798 NSi001-ANSi001-BNSi001-C 2022-00-00 2022-00-00 PubMed: 36313423 DOI: 10.3389/fgene.2022.1007519 -
Perepelina K, Zaytseva A, Khudiakov A, Neganova I, Vasichkina E, Malashicheva A, Kostareva A
LMNA mutation leads to cardiac sodium channel dysfunction in the Emery-Dreifuss muscular dystrophy patient
Perepelina K et al. LMNA mutation leads to cardiac sodium channel dysfunction in the Emery-Dreifuss muscular dystrophy patient. . 2022-00-00. Pubmed ID: 35935653; DOI: 10.3389/fcvm.2022.932956; PMC: PMC9355377 WTSIi004-AFAMRCi007-AFAMRCi007-B 2022-00-00 2022-00-00 PubMed: 35935653 DOI: 10.3389/fcvm.2022.932956Associated cell lines:
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Sozzi E, Kajtez J, Bruzelius A, Wesseler MF, Nilsson F, Birtele M, Larsen NB, Ottosson DR, Storm P, Parmar M, Fiorenzano A
Silk scaffolding drives self-assembly of functional and mature human brain organoids
Sozzi E et al. Silk scaffolding drives self-assembly of functional and mature human brain organoids. . 2022-00-00. Pubmed ID: 36313550; DOI: 10.3389/fcell.2022.1023279; PMC: PMC9614032 RCe021-A 2022-00-00 2022-00-00 PubMed: 36313550 DOI: 10.3389/fcell.2022.1023279Associated cell lines:
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Gridina MM, Shitik EM, Lemskaya NA, Minina JM, Grishchenko IV, Dolskiy AA, Shorina AR, Maksimova YV, Yudkin DV
Derivation of iPS cell line (ICGi032-A) from a patient affected with fragile X syndrome
Gridina MM et al. Derivation of iPS cell line (ICGi032-A) from a patient affected with fragile X syndrome. . 2021-12-00. Pubmed ID: 34864218; DOI: 10.1016/j.scr.2021.102615 IMGTi003-AICGi032-A 2021-12-00 2021-12-00 PubMed: 34864218 DOI: 10.1016/j.scr.2021.102615Associated cell lines:
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Kumari Ankita, Chaudhary Archana, Haque Rizwanul
Induced Pluripotent Stem Cells for the Treatment of Neurodegenerative Disease: Current and Future Prospects
Kumari Ankita et al. Induced Pluripotent Stem Cells for the Treatment of Neurodegenerative Disease: Current and Future Prospects. . 2022-00-00. DOI: 10.1007/978-981-16-8562-0_5 CSSi004-A 2022-00-00 2022-00-00 DOI: 10.1007/978-981-16-8562-0_5Associated cell lines:
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Souralova T, Holubcova Z, Kyjovska D, Hampl A, Koutna I
Xeno- and feeder-free derivation of two sex-discordant sibling lines of human embryonic stem cells
Souralova T et al. Xeno- and feeder-free derivation of two sex-discordant sibling lines of human embryonic stem cells. . 2021-12-00. Pubmed ID: 34715503; DOI: 10.1016/j.scr.2021.102574 MUNIe008-AMUNIe009-A 2021-12-00 2021-12-00 PubMed: 34715503 DOI: 10.1016/j.scr.2021.102574Associated cell lines:
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Coombs GS, Rios-Monterrosa JL, Lai S, Dai Q, Goll AC, Ketterer MR, Valdes MF, Uche N, Benjamin IJ, Wallrath LL
Modulation of muscle redox and protein aggregation rescues lethality caused by mutant lamins
Coombs GS et al. Modulation of muscle redox and protein aggregation rescues lethality caused by mutant lamins. . 2021-11-25. Pubmed ID: 34872044; DOI: 10.1016/j.redox.2021.102196; PMC: PMC8646998 YCMi003-A 2021-11-25 2021-11-25 PubMed: 34872044 DOI: 10.1016/j.redox.2021.102196Associated cell lines:
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Pereira Sena P, Weber JJ, Watchon M, Robinson KJ, Wassouf Z, Hauser S, Helm J, Abeditashi M, Schmidt J, Hübener-Schmid J, Schöls L, Laird AS, Riess O, Schmidt T
Pathophysiological interplay between O-GlcNAc transferase and the Machado-Joseph disease protein ataxin-3
Pereira Sena P et al. Pathophysiological interplay between O-GlcNAc transferase and the Machado-Joseph disease protein ataxin-3. . 2021-11-23. Pubmed ID: 34785590; DOI: 10.1073/pnas.2025810118; PMC: PMC8617493 HIHCNi002-A 2021-11-23 2021-11-23 PubMed: 34785590 DOI: 10.1073/pnas.2025810118Associated cell lines:
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Mairot K, Smirnov V, Bocquet B, Labesse G, Arndt C, Defoort-Dhellemmes S, Zanlonghi X, Hamroun D, Denis D, Picot MC, David T, Grunewald O, Pégart M, Huguet H, Roux AF, Kalatzis V, Dhaenens CM, Meunier I
CRB1-Related Retinal Dystrophies in a Cohort of 50 Patients: A Reappraisal in the Light of Specific Müller Cell and Photoreceptor CRB1 Isoforms
Mairot K et al. CRB1-Related Retinal Dystrophies in a Cohort of 50 Patients: A Reappraisal in the Light of Specific Müller Cell and Photoreceptor CRB1 Isoforms. . 2021-11-23. Pubmed ID: 34884448; DOI: 10.3390/ijms222312642; PMC: PMC8657784 ESi082-A 2021-11-23 2021-11-23 PubMed: 34884448 DOI: 10.3390/ijms222312642Associated cell lines:
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Wintering A, Dvorak CC, Stieglitz E, Loh ML
Juvenile myelomonocytic leukemia in the molecular era: a clinician's guide to diagnosis, risk stratification, and treatment
Wintering A et al. Juvenile myelomonocytic leukemia in the molecular era: a clinician's guide to diagnosis, risk stratification, and treatment. . 2021-11-23. Pubmed ID: 34525182; DOI: 10.1182/bloodadvances.2021005117; PMC: PMC8759142 CHOPi001-A 2021-11-23 2021-11-23 PubMed: 34525182 DOI: 10.1182/bloodadvances.2021005117Associated cell lines:
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Vogiatzis S, Celestino M, Trevisan M, Magro G, Del Vecchio C, Erdengiz D, Palù G, Parolin C, Maguire-Zeiss K, Calistri A
Lentiviral Vectors Expressing Chimeric NEDD4 Ubiquitin Ligases: An Innovative Approach for Interfering with Alpha-Synuclein Accumulation
Vogiatzis S et al. Lentiviral Vectors Expressing Chimeric NEDD4 Ubiquitin Ligases: An Innovative Approach for Interfering with Alpha-Synuclein Accumulation. . 2021-11-21. Pubmed ID: 34831478; DOI: 10.3390/cells10113256; PMC: PMC8624294 UNIPDi007-A 2021-11-21 2021-11-21 PubMed: 34831478 DOI: 10.3390/cells10113256Associated cell lines:
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Moser VA, Workman MJ, Hurwitz SJ, Lipman RM, Pike CJ, Svendsen CN
Microglial transcription profiles in mouse and human are driven by APOE4 and sex
Moser VA et al. Microglial transcription profiles in mouse and human are driven by APOE4 and sex. . 2021-11-19. Pubmed ID: 34746703; DOI: 10.1016/j.isci.2021.103238; PMC: PMC8551075 EDi022-AEDi023-AEDi028-AEDi029-AEDi034-AEDi035-AEDi036-AEDi042-AEDi044-A 2021-11-19 2021-11-19 PubMed: 34746703 DOI: 10.1016/j.isci.2021.103238 -
Pratumkaew P, Issaragrisil S, Luanpitpong S
Induced Pluripotent Stem Cells as a Tool for Modeling Hematologic Disorders and as a Potential Source for Cell-Based Therapies
Pratumkaew P et al. Induced Pluripotent Stem Cells as a Tool for Modeling Hematologic Disorders and as a Potential Source for Cell-Based Therapies. . 2021-11-19. Pubmed ID: 34831472; DOI: 10.3390/cells10113250; PMC: PMC8623953 MUSIi008-A 2021-11-19 2021-11-19 PubMed: 34831472 DOI: 10.3390/cells10113250Associated cell lines:
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Hopkins HK, Traverse EM, Barr KL
Methodologies for Generating Brain Organoids to Model Viral Pathogenesis in the CNS
Hopkins HK et al. Methodologies for Generating Brain Organoids to Model Viral Pathogenesis in the CNS. . 2021-11-19. Pubmed ID: 34832665; DOI: 10.3390/pathogens10111510; PMC: PMC8625030 KMUe003-A 2021-11-19 2021-11-19 PubMed: 34832665 DOI: 10.3390/pathogens10111510Associated cell lines:
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Anderson RH, Sochacki KA, Vuppula H, Scott BL, Bailey EM, Schultz MM, Kerkvliet JG, Taraska JW, Hoppe AD, Francis KR
Sterols lower energetic barriers of membrane bending and fission necessary for efficient clathrin-mediated endocytosis
Anderson RH et al. Sterols lower energetic barriers of membrane bending and fission necessary for efficient clathrin-mediated endocytosis. . 2021-11-16. Pubmed ID: 34788623; DOI: 10.1016/j.celrep.2021.110008; PMC: PMC8620193 CRMi001-ACRMi001-A-1 2021-11-16 2021-11-16 PubMed: 34788623 DOI: 10.1016/j.celrep.2021.110008Associated cell lines:
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Iop L, Iliceto S, Civieri G, Tona F
Inherited and Acquired Rhythm Disturbances in Sick Sinus Syndrome, Brugada Syndrome, and Atrial Fibrillation: Lessons from Preclinical Modeling
Iop L et al. Inherited and Acquired Rhythm Disturbances in Sick Sinus Syndrome, Brugada Syndrome, and Atrial Fibrillation: Lessons from Preclinical Modeling. . 2021-11-15. Pubmed ID: 34831398; DOI: 10.3390/cells10113175; PMC: PMC8623957 FAMRCi004-AFAMRCi004-BIBMSi013-AIBMSi014-AIBMSi015-AJSPHi001-A 2021-11-15 2021-11-15 PubMed: 34831398 DOI: 10.3390/cells10113175Associated cell lines:
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Robbins M, Pisupati V, Azzarelli R, Nehme SI, Barker RA, Fruk L, Schierle GSK
Biofunctionalised bacterial cellulose scaffold supports the patterning and expansion of human embryonic stem cell-derived dopaminergic progenitor cells
Robbins M et al. Biofunctionalised bacterial cellulose scaffold supports the patterning and expansion of human embryonic stem cell-derived dopaminergic progenitor cells. . 2021-11-13. Pubmed ID: 34774094; DOI: 10.1186/s13287-021-02639-5; PMC: PMC8590306 RCe021-A 2021-11-13 2021-11-13 PubMed: 34774094 DOI: 10.1186/s13287-021-02639-5Associated cell lines:
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Eggenschwiler R, Gschwendtberger T, Felski C, Jahn C, Langer F, Sterneckert J, Hermann A, Lühmann J, Steinemann D, Haase A, Martin U, Petri S, Cantz T
A selectable all-in-one CRISPR prime editing piggyBac transposon allows for highly efficient gene editing in human cell lines
Eggenschwiler R et al. A selectable all-in-one CRISPR prime editing piggyBac transposon allows for highly efficient gene editing in human cell lines. . 2021-11-12. Pubmed ID: 34773059; DOI: 10.1038/s41598-021-01689-2; PMC: PMC8589839 MHHi001-A 2021-11-12 2021-11-12 PubMed: 34773059 DOI: 10.1038/s41598-021-01689-2Associated cell lines:
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de Souza AF, Bressan FF, Pieri NCG, Botigelli RC, Revay T, Haddad SK, Covas DT, Ramos ES, King WA, Meirelles FV
Generation of Primordial Germ Cell-like Cells from iPSCs Derived from Turner Syndrome Patients
de Souza AF et al. Generation of Primordial Germ Cell-like Cells from iPSCs Derived from Turner Syndrome Patients. . 2021-11-10. Pubmed ID: 34831322; DOI: 10.3390/cells10113099; PMC: PMC8624672 TUSMi008-A 2021-11-10 2021-11-10 PubMed: 34831322 DOI: 10.3390/cells10113099Associated cell lines:
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Völkner C, Liedtke M, Untucht R, Hermann A, Frech MJ
Patient-Specific iPSC-Derived Neural Differentiated and Hepatocyte-like Cells, Carrying the Compound Heterozygous Mutation p.V1023Sfs*15/p.G992R, Present the "Variant" Biochemical Phenotype of Niemann-Pick Type C1 Disease
Völkner C et al. Patient-Specific iPSC-Derived Neural Differentiated and Hepatocyte-like Cells, Carrying the Compound Heterozygous Mutation p.V1023Sfs*15/p.G992R, Present the "Variant" Biochemical Phenotype of Niemann-Pick Type C1 Disease. . 2021-11-10. Pubmed ID: 34830064; DOI: 10.3390/ijms222212184; PMC: PMC8624182 AKOSi004-AAKOSi005-A 2021-11-10 2021-11-10 PubMed: 34830064 DOI: 10.3390/ijms222212184Associated cell lines:
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Ren J, Li C, Zhang M, Wang H, Xie Y, Tang Y
A Step-by-Step Refined Strategy for Highly Efficient Generation of Neural Progenitors and Motor Neurons from Human Pluripotent Stem Cells
Ren J et al. A Step-by-Step Refined Strategy for Highly Efficient Generation of Neural Progenitors and Motor Neurons from Human Pluripotent Stem Cells. . 2021-11-09. Pubmed ID: 34831309; DOI: 10.3390/cells10113087; PMC: PMC8625124 CSUi002-A 2021-11-09 2021-11-09 PubMed: 34831309 DOI: 10.3390/cells10113087Associated cell lines:
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Barbuti PA, Ohnmacht J, Santos BFR, Antony PM, Massart F, Cruciani G, Dording CM, Pavelka L, Casadei N, Kwon YJ, Krüger R
Gene-corrected p.A30P SNCA patient-derived isogenic neurons rescue neuronal branching and function
Barbuti PA et al. Gene-corrected p.A30P SNCA patient-derived isogenic neurons rescue neuronal branching and function. . 2021-11-09. Pubmed ID: 34754035; DOI: 10.1038/s41598-021-01505-x; PMC: PMC8578337 HIHDNDi001-AHIHDNDi001-B 2021-11-09 2021-11-09 PubMed: 34754035 DOI: 10.1038/s41598-021-01505-xAssociated cell lines:
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Mukherjee S, French DL, Gadue P
Loss of TBX3 enhances pancreatic progenitor generation from human pluripotent stem cells
Mukherjee S et al. Loss of TBX3 enhances pancreatic progenitor generation from human pluripotent stem cells. . 2021-11-09. Pubmed ID: 34653400; DOI: 10.1016/j.stemcr.2021.09.004; PMC: PMC8580886 CHOPi004-A 2021-11-09 2021-11-09 PubMed: 34653400 DOI: 10.1016/j.stemcr.2021.09.004Associated cell lines:
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Oosterveen T, Garção P, Moles-Garcia E, Soleilhavoup C, Travaglio M, Sheraz S, Peltrini R, Patrick K, Labas V, Combes-Soia L, Marklund U, Hohenstein P, Panman L
Pluripotent stem cell derived dopaminergic subpopulations model the selective neuron degeneration in Parkinson's disease
Oosterveen T et al. Pluripotent stem cell derived dopaminergic subpopulations model the selective neuron degeneration in Parkinson's disease. . 2021-11-09. Pubmed ID: 34678205; DOI: 10.1016/j.stemcr.2021.09.014; PMC: PMC8581055 EDi001-A 2021-11-09 2021-11-09 PubMed: 34678205 DOI: 10.1016/j.stemcr.2021.09.014Associated cell lines:
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Olschok K, Han L, de Toledo MAS, Böhnke J, Graßhoff M, Costa IG, Theocharides A, Maurer A, Schüler HM, Buhl EM, Pannen K, Baumeister J, Kalmer M, Gupta S, Boor P, Gezer D, Brümmendorf TH, Zenke M, Chatain N, Koschmieder S
CALR frameshift mutations in MPN patient-derived iPSCs accelerate maturation of megakaryocytes
Olschok K et al. CALR frameshift mutations in MPN patient-derived iPSCs accelerate maturation of megakaryocytes. . 2021-11-09. Pubmed ID: 34678208; DOI: 10.1016/j.stemcr.2021.09.019; PMC: PMC8581168 INCABRi002-A 2021-11-09 2021-11-09 PubMed: 34678208 DOI: 10.1016/j.stemcr.2021.09.019Associated cell lines:
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Hwang JJ, Choi J, Rim YA, Nam Y, Ju JH
Application of Induced Pluripotent Stem Cells for Disease Modeling and 3D Model Construction: Focus on Osteoarthritis
Hwang JJ et al. Application of Induced Pluripotent Stem Cells for Disease Modeling and 3D Model Construction: Focus on Osteoarthritis. . 2021-11-05. Pubmed ID: 34831254; DOI: 10.3390/cells10113032; PMC: PMC8622662 CIBi009-A 2021-11-05 2021-11-05 PubMed: 34831254 DOI: 10.3390/cells10113032Associated cell lines:
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Fomin Andrey, Gärtner Anna, Cyganek Lukas, Tiburcy Malte, Tuleta Izabela, Wellers Luisa, Folsche Lina, Hobbach Anastasia J., von Frieling-Salewsky Marion, Unger Andreas, Hucke Anna, Koser Franziska, Kassner Astrid, Sielemann Katharina, Streckfuß-Bömeke Katrin, Hasenfuss Gerd, Goedel Alexander, Laugwitz Karl-Ludwig, Moretti Alessandra, Gummert Jan F., dos Remedios Cristobal G., Reinecke Holger, Knöll Ralph, van Heesch Sebastiaan, Hubner Norbert, Zimmermann Wolfram H., Milting Hendrik, Linke Wolfgang A.
Truncated titin proteins and titin haploinsufficiency are targets for functional recovery in human cardiomyopathy due toTTNmutations
Fomin Andrey et al. Truncated titin proteins and titin haploinsufficiency are targets for functional recovery in human cardiomyopathy due toTTNmutations. . 2021-11-03. DOI: 10.1126/scitranslmed.abd3079 MRIi010-A 2021-11-03 2021-11-03 DOI: 10.1126/scitranslmed.abd3079Associated cell lines:
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Kyrousi C, O'Neill AC, Brazovskaja A, He Z, Kielkowski P, Coquand L, Di Giaimo R, D' Andrea P, Belka A, Forero Echeverry A, Mei D, Lenge M, Cruceanu C, Buchsbaum IY, Khattak S, Fabien G, Binder E, Elmslie F, Guerrini R, Baffet AD, Sieber SA, Treutlein B, Robertson SP, Cappello S
Extracellular LGALS3BP regulates neural progenitor position and relates to human cortical complexity
Kyrousi C et al. Extracellular LGALS3BP regulates neural progenitor position and relates to human cortical complexity. . 2021-11-02. Pubmed ID: 34728600; DOI: 10.1038/s41467-021-26447-w; PMC: PMC8564519 ISFi001-A 2021-11-02 2021-11-02 PubMed: 34728600 DOI: 10.1038/s41467-021-26447-wAssociated cell lines:
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Kalayinia S, Maleki M, Mahdavi M, Mahdieh N
Whole-Exome Sequencing Reveals a Novel Mutation of FLNA Gene in an Iranian Family with Nonsyndromic Tetralogy of Fallot
Kalayinia S et al. Whole-Exome Sequencing Reveals a Novel Mutation of FLNA Gene in an Iranian Family with Nonsyndromic Tetralogy of Fallot. . 2021-11-02. Pubmed ID: 33942857; DOI: 10.1093/labmed/lmab018 YAHKMUi001-A 2021-11-02 2021-11-02 PubMed: 33942857 DOI: 10.1093/labmed/lmab018Associated cell lines:
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Xu L.
Stem cell therapy in the treatment of premature ovarian failure
Xu L.. Stem cell therapy in the treatment of premature ovarian failure. . 2021-11-01. DOI: 10.3760/cma.j.cn101441-20200901-00471 NTUHi001-A 2021-11-01 2021-11-01 DOI: 10.3760/cma.j.cn101441-20200901-00471Associated cell lines:
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Wang Z, Zheng J, Pan R, Chen Y
Current status and future prospects of patient-derived induced pluripotent stem cells
Wang Z et al. Current status and future prospects of patient-derived induced pluripotent stem cells. . 2021-11-00. Pubmed ID: 34378170; DOI: 10.1007/s13577-021-00592-2 REGUi003-ACSUXHi002-ASKLOi001-AMPIi006-A 2021-11-00 2021-11-00 PubMed: 34378170 DOI: 10.1007/s13577-021-00592-2Associated cell lines:
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Eastlake K, Lamb WDB, Luis J, Khaw PT, Jayaram H, Limb GA
Prospects for the application of Müller glia and their derivatives in retinal regenerative therapies
Eastlake K et al. Prospects for the application of Müller glia and their derivatives in retinal regenerative therapies. . 2021-11-00. Pubmed ID: 33930561; DOI: 10.1016/j.preteyeres.2021.100970 RCe013-A 2021-11-00 2021-11-00 PubMed: 33930561 DOI: 10.1016/j.preteyeres.2021.100970Associated cell lines:
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Khurana P, Kolundzic N, Flohr C, Ilic D
Human pluripotent stem cells: An alternative for 3D in vitro modelling of skin disease
Khurana P et al. Human pluripotent stem cells: An alternative for 3D in vitro modelling of skin disease. . 2021-11-00. Pubmed ID: 33864704; DOI: 10.1111/exd.14358 KCLi001-AKCLi002-AKCLi003-A 2021-11-00 2021-11-00 PubMed: 33864704 DOI: 10.1111/exd.14358 -
Ohira M, Kikuchi E, Mizuta S, Yoshida N, Onodera M, Nakanishi M, Okuyama T, Mashima R
Production of therapeutic iduronate-2-sulfatase enzyme with a novel single-stranded RNA virus vector
Ohira M et al. Production of therapeutic iduronate-2-sulfatase enzyme with a novel single-stranded RNA virus vector. . 2021-11-00. Pubmed ID: 34480399; DOI: 10.1111/gtc.12894 UNIGEi001-A 2021-11-00 2021-11-00 PubMed: 34480399 DOI: 10.1111/gtc.12894Associated cell lines:
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Hollý D, Klein M, Mazreku M, Zamborský R, Polák Š, Danišovič Ľ, Csöbönyeiová M
Stem Cells and Their Derivatives-Implications for Alveolar Bone Regeneration: A Comprehensive Review
Hollý D et al. Stem Cells and Their Derivatives-Implications for Alveolar Bone Regeneration: A Comprehensive Review. . 2021-10-29. Pubmed ID: 34769175; DOI: 10.3390/ijms222111746; PMC: PMC8583713 UNIPDi001-A 2021-10-29 2021-10-29 PubMed: 34769175 DOI: 10.3390/ijms222111746Associated cell lines:
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Wang X, Qu M, Li Z, Long Y, Hong K, Li H
Valproic acid promotes the in vitro differentiation of human pluripotent stem cells into spermatogonial stem cell-like cells
Wang X et al. Valproic acid promotes the in vitro differentiation of human pluripotent stem cells into spermatogonial stem cell-like cells. . 2021-10-29. Pubmed ID: 34715904; DOI: 10.1186/s13287-021-02621-1; PMC: PMC8555208 HUSTi001-A 2021-10-29 2021-10-29 PubMed: 34715904 DOI: 10.1186/s13287-021-02621-1Associated cell lines:
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Hoffmann PC, Giandomenico SL, Ganeva I, Wozny MR, Sutcliffe M, Lancaster MA, Kukulski W
Electron cryo-tomography reveals the subcellular architecture of growing axons in human brain organoids
Hoffmann PC et al. Electron cryo-tomography reveals the subcellular architecture of growing axons in human brain organoids. . 2021-10-26. Pubmed ID: 34698018; DOI: 10.7554/elife.70269; PMC: PMC8547956 WAe009-A 2021-10-26 2021-10-26 PubMed: 34698018 DOI: 10.7554/elife.70269Associated cell lines:
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Yang X.
Research progress in cell and animal models of Leber hereditary optic neuropathy
Yang X.. Research progress in cell and animal models of Leber hereditary optic neuropathy. . 2021-10-25. DOI: 10.3760/cma.j.cn511434-20210207-00073 FINCBi001-A 2021-10-25 2021-10-25 DOI: 10.3760/cma.j.cn511434-20210207-00073Associated cell lines:
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Mallach A, Gobom J, Arber C, Piers TM, Hardy J, Wray S, Zetterberg H, Pocock J
Differential Stimulation of Pluripotent Stem Cell-Derived Human Microglia Leads to Exosomal Proteomic Changes Affecting Neurons
Mallach A et al. Differential Stimulation of Pluripotent Stem Cell-Derived Human Microglia Leads to Exosomal Proteomic Changes Affecting Neurons. . 2021-10-24. Pubmed ID: 34831089; DOI: 10.3390/cells10112866; PMC: PMC8616378 BIONi010-CRBi001-A 2021-10-24 2021-10-24 PubMed: 34831089 DOI: 10.3390/cells10112866Associated cell lines:
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Jaiswal SK, Raj S, DePamphilis ML
Developmental Acquisition of p53 Functions
Jaiswal SK et al. Developmental Acquisition of p53 Functions. . 2021-10-23. Pubmed ID: 34828285; DOI: 10.3390/genes12111675; PMC: PMC8622856 NERCe003-ANERCe003-A-3 2021-10-23 2021-10-23 PubMed: 34828285 DOI: 10.3390/genes12111675Associated cell lines:
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Dehshahri A, Biagioni A, Bayat H, Lee EHC, Hashemabadi M, Fekri HS, Zarrabi A, Mohammadinejad R, Kumar AP
Editing SOX Genes by CRISPR-Cas: Current Insights and Future Perspectives
Dehshahri A et al. Editing SOX Genes by CRISPR-Cas: Current Insights and Future Perspectives. . 2021-10-20. Pubmed ID: 34768751; DOI: 10.3390/ijms222111321; PMC: PMC8583549 GIBHe001-A 2021-10-20 2021-10-20 PubMed: 34768751 DOI: 10.3390/ijms222111321Associated cell lines:
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Morsy A, Carmona AV, Trippier PC
Patient-Derived Induced Pluripotent Stem Cell Models for Phenotypic Screening in the Neuronal Ceroid Lipofuscinoses
Morsy A et al. Patient-Derived Induced Pluripotent Stem Cell Models for Phenotypic Screening in the Neuronal Ceroid Lipofuscinoses. . 2021-10-15. Pubmed ID: 34684815; DOI: 10.3390/molecules26206235; PMC: PMC8538546 LEIi004-ALEIi004-A-1 2021-10-15 2021-10-15 PubMed: 34684815 DOI: 10.3390/molecules26206235Associated cell lines:
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Bergström P, Trybala E, Eriksson CE, Johansson M, Satir TM, Widéhn S, Fruhwürth S, Michno W, Nazir FH, Hanrieder J, Paludan SR, Agholme L, Zetterberg H, Bergström T
Herpes Simplex Virus 1 and 2 Infections during Differentiation of Human Cortical Neurons
Bergström P et al. Herpes Simplex Virus 1 and 2 Infections during Differentiation of Human Cortical Neurons. . 2021-10-14. Pubmed ID: 34696502; DOI: 10.3390/v13102072; PMC: PMC8540961 WTSIi015-A 2021-10-14 2021-10-14 PubMed: 34696502 DOI: 10.3390/v13102072Associated cell lines:
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Masumoto J, Zhou W, Morikawa S, Hosokawa S, Taguchi H, Yamamoto T, Kurata M, Kaneko N
Molecular biology of autoinflammatory diseases
Masumoto J et al. Molecular biology of autoinflammatory diseases. . 2021-10-11. Pubmed ID: 34635190; DOI: 10.1186/s41232-021-00181-8; PMC: PMC8507398 NIHTVBi014-A 2021-10-11 2021-10-11 PubMed: 34635190 DOI: 10.1186/s41232-021-00181-8Associated cell lines:
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Botor M, Fus-Kujawa A, Uroczynska M, Stepien KL, Galicka A, Gawron K, Sieron AL
Osteogenesis Imperfecta: Current and Prospective Therapies
Botor M et al. Osteogenesis Imperfecta: Current and Prospective Therapies. . 2021-10-10. Pubmed ID: 34680126; DOI: 10.3390/biom11101493; PMC: PMC8533546 MCRIi001-AMCRIi001-A-1KSCBi006-A 2021-10-10 2021-10-10 PubMed: 34680126 DOI: 10.3390/biom11101493Associated cell lines:
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Sidhu I, Barwe SP, Pillai RK, Gopalakrishnapillai A
Harnessing the Power of Induced Pluripotent Stem Cells and Gene Editing Technology: Therapeutic Implications in Hematological Malignancies
Sidhu I et al. Harnessing the Power of Induced Pluripotent Stem Cells and Gene Editing Technology: Therapeutic Implications in Hematological Malignancies. . 2021-10-09. Pubmed ID: 34685678; DOI: 10.3390/cells10102698; PMC: PMC8534597 KUMCi002-A 2021-10-09 2021-10-09 PubMed: 34685678 DOI: 10.3390/cells10102698Associated cell lines:
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Xu Y, Tao J, Yu X, Wu Y, Chen Y, You K, Zhang J, Getachew A, Pan T, Zhuang Y, Yuan F, Yang F, Lin X, Li YX
Hypomorphic ASGR1 modulates lipid homeostasis via INSIG1-mediated SREBP signaling suppression
Xu Y et al. Hypomorphic ASGR1 modulates lipid homeostasis via INSIG1-mediated SREBP signaling suppression. . 2021-10-08. Pubmed ID: 34622799; DOI: 10.1172/jci.insight.147038; PMC: PMC8525641 WAe001-AWAe001-A-6 2021-10-08 2021-10-08 PubMed: 34622799 DOI: 10.1172/jci.insight.147038Associated cell lines:
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Obst J, Hall-Roberts HL, Smith TB, Kreuzer M, Magno L, Di Daniel E, Davis JB, Mead E
PLCγ2 regulates TREM2 signalling and integrin-mediated adhesion and migration of human iPSC-derived macrophages
Obst J et al. PLCγ2 regulates TREM2 signalling and integrin-mediated adhesion and migration of human iPSC-derived macrophages. . 2021-10-06. Pubmed ID: 34615897; DOI: 10.1038/s41598-021-96144-7; PMC: PMC8494732 BIONi010-CBIONi010-C-17 2021-10-06 2021-10-06 PubMed: 34615897 DOI: 10.1038/s41598-021-96144-7Associated cell lines:
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Huang W, Cheng YS, Yang S, Swaroop M, Xu M, Huang W, Zheng W
Disease modeling for Mucopolysaccharidosis type IIIB using patient derived induced pluripotent stem cells
Huang W et al. Disease modeling for Mucopolysaccharidosis type IIIB using patient derived induced pluripotent stem cells. . 2021-10-01. Pubmed ID: 34411609; DOI: 10.1016/j.yexcr.2021.112785; PMC: PMC8440473 TRNDi006-A 2021-10-01 2021-10-01 PubMed: 34411609 DOI: 10.1016/j.yexcr.2021.112785Associated cell lines:
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Han Ji Yeon, Lee Seungbok, Woo Hyewon, Kim Soo Yeon, Kim Hunmin, Lim Byung Chan, Hwang Hee, Choi Jieun, Kim Ki Joong, Chae Jong-Hee
Heterogeneous Clinical Characteristics of Allan-Herndon-Dudley Syndrome with SLC16A2 Mutations
Han Ji Yeon et al. Heterogeneous Clinical Characteristics of Allan-Herndon-Dudley Syndrome with SLC16A2 Mutations. . 2021-10-01. DOI: 10.26815/acn.2021.00423 SHCDNi003-A 2021-10-01 2021-10-01 DOI: 10.26815/acn.2021.00423Associated cell lines:
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Zheng J, Li G, Qin M
Generation of induced pluripotent stem cell, BCHSCTi001-A, derived from a Hemophilia A patient with F8 (p. R391C) mutation
Zheng J et al. Generation of induced pluripotent stem cell, BCHSCTi001-A, derived from a Hemophilia A patient with F8 (p. R391C) mutation. . 2021-10-00. Pubmed ID: 34496342; DOI: 10.1016/j.scr.2021.102491 BCHSCTi001-A 2021-10-00 2021-10-00 PubMed: 34496342 DOI: 10.1016/j.scr.2021.102491Associated cell lines:
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Zhou M, Xing Q, Zhang D, Zhang C, Zhang Y, Zhang J, Shan Y
Generation of an Akaluc knock-in human embryonic stem cell reporter line using CRISPR-Cas9 technology
Zhou M et al. Generation of an Akaluc knock-in human embryonic stem cell reporter line using CRISPR-Cas9 technology. . 2021-10-00. Pubmed ID: 34509917; DOI: 10.1016/j.scr.2021.102532 WAe001-A-66 2021-10-00 2021-10-00 PubMed: 34509917 DOI: 10.1016/j.scr.2021.102532Associated cell lines:
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Xu S, Liu X, Liu X, Shi Y, Jin X, Zhang N, Li X, Zhang H
Wedelolactone ameliorates Pseudomonas aeruginosa-induced inflammation and corneal injury by suppressing caspase-4/5/11/GSDMD-mediated non-canonical pyroptosis
Xu S et al. Wedelolactone ameliorates Pseudomonas aeruginosa-induced inflammation and corneal injury by suppressing caspase-4/5/11/GSDMD-mediated non-canonical pyroptosis. . 2021-10-00. Pubmed ID: 34481822; DOI: 10.1016/j.exer.2021.108750 HMUi001-A 2021-10-00 2021-10-00 PubMed: 34481822 DOI: 10.1016/j.exer.2021.108750Associated cell lines:
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Guo H, Jin ZL, Yao X, Park J, Gwon YP, Kim S, Kim KP, Cui XS, Kim NH, Yoo H, Han DW
Derivation of iPSC lines from two idiopathic ASD patients (OFi001-A, OFi002-A)
Guo H et al. Derivation of iPSC lines from two idiopathic ASD patients (OFi001-A, OFi002-A). . 2021-10-00. Pubmed ID: 34438162; DOI: 10.1016/j.scr.2021.102510 OFi001-AOFi002-A 2021-10-00 2021-10-00 PubMed: 34438162 DOI: 10.1016/j.scr.2021.102510 -
Al-Shehri M, Baadhaim M, Jamalalddin S, Aboalola D, Daghestani M, AlZahrani H, Malibari D, Mubaraki M, Aldubayan K, AlBalwi M, Alsayegh K
Generation of induced pluripotent stem cell Line KAIMRCi001-A by reprogramming erythroid progenitors from peripheral blood of a healthy Saudi donor
Al-Shehri M et al. Generation of induced pluripotent stem cell Line KAIMRCi001-A by reprogramming erythroid progenitors from peripheral blood of a healthy Saudi donor. . 2021-10-00. Pubmed ID: 34592601; DOI: 10.1016/j.scr.2021.102548 KAIMRCi001-A 2021-10-00 2021-10-00 PubMed: 34592601 DOI: 10.1016/j.scr.2021.102548Associated cell lines:
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Wang L, Li H, Li Y, Xu M, Lin J, Liao Z, Pei Z, Zhang C
Generation and characterization of an induced pluripotent stem cell line (ZSYYDNi001-A) from a patient with Duchenne muscular dystrophy carrying exon 51 deletion in the DMD gene
Wang L et al. Generation and characterization of an induced pluripotent stem cell line (ZSYYDNi001-A) from a patient with Duchenne muscular dystrophy carrying exon 51 deletion in the DMD gene. . 2021-10-00. Pubmed ID: 34619646; DOI: 10.1016/j.scr.2021.102553 ZSYYDNi001-A 2021-10-00 2021-10-00 PubMed: 34619646 DOI: 10.1016/j.scr.2021.102553Associated cell lines:
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Temocin O, Regele D, Sathianathan M, Überbacher C, Hartl M, Edenhofer F, Meyer D
Generation of an hiPSC-1 knock-in line expressing TY1-tagged MNX1-protein together with mScarlet
Temocin O et al. Generation of an hiPSC-1 knock-in line expressing TY1-tagged MNX1-protein together with mScarlet. . 2021-10-00. Pubmed ID: 34509159; DOI: 10.1016/j.scr.2021.102522 IBKMOLi001-A 2021-10-00 2021-10-00 PubMed: 34509159 DOI: 10.1016/j.scr.2021.102522Associated cell lines:
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Miyake T, Kuge M, Matsumoto Y, Shimada M
α-glucosyl-rutin activates immediate early genes in human induced pluripotent stem cells
Miyake T et al. α-glucosyl-rutin activates immediate early genes in human induced pluripotent stem cells. . 2021-10-00. Pubmed ID: 34455240; DOI: 10.1016/j.scr.2021.102511 KUIFMSi004-C 2021-10-00 2021-10-00 PubMed: 34455240 DOI: 10.1016/j.scr.2021.102511Associated cell lines:
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Neyrinck K, Van Den Daele J, Vervliet T, De Smedt J, Wierda K, Nijs M, Vanbokhoven T, D'hondt A, Planque M, Fendt SM, Shih PY, Seibt F, Almenar JP, Kreir M, Kumar D, Broccoli V, Bultynck G, Ebneth A, Cabrera-Socorro A, Verfaillie C
SOX9-induced Generation of Functional Astrocytes Supporting Neuronal Maturation in an All-human System
Neyrinck K et al. SOX9-induced Generation of Functional Astrocytes Supporting Neuronal Maturation in an All-human System. . 2021-10-00. Pubmed ID: 33982246; DOI: 10.1007/s12015-021-10179-x; PMC: PMC8553725 SIGi001-ASIGi001-A-20 2021-10-00 2021-10-00 PubMed: 33982246 DOI: 10.1007/s12015-021-10179-xAssociated cell lines:
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Ovchinnikov Dmitry
Reprogramming fibroblasts and mononuclear blood cells into iPSCs using Sendai virus v1
Ovchinnikov Dmitry. Reprogramming fibroblasts and mononuclear blood cells into iPSCs using Sendai virus v1. . 2021-09-30. DOI: 10.17504/protocols.io.bypqpvmw FINi002-A 2021-09-30 2021-09-30 DOI: 10.17504/protocols.io.bypqpvmwAssociated cell lines:
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Krumm L, Pozner T, Kaindl J, Regensburger M, Günther C, Turan S, Asadollahi R, Rauch A, Winner B
Generation and characterization of an endogenously tagged SPG11-human iPSC line by CRISPR/Cas9 mediated knock-in
Krumm L et al. Generation and characterization of an endogenously tagged SPG11-human iPSC line by CRISPR/Cas9 mediated knock-in. . 2021-10-00. Pubmed ID: 34479069; DOI: 10.1016/j.scr.2021.102520 TMOi001-ATMOi001-A-4 2021-10-00 2021-10-00 PubMed: 34479069 DOI: 10.1016/j.scr.2021.102520Associated cell lines:
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Wang T, Zhou Y, Zhou R, Huang W, Wang J, Li H, Lei M, Tan X, Zhang Y
Generation of induced pluripotent stem cells (iPSCs) from a Chinese infant (XACHi015-A) with type 2 Long QT syndrome carrying the heterozygous mutation c.1814C>T(p.P605L) in KCNH2
Wang T et al. Generation of induced pluripotent stem cells (iPSCs) from a Chinese infant (XACHi015-A) with type 2 Long QT syndrome carrying the heterozygous mutation c.1814C>T(p.P605L) in KCNH2. . 2021-10-00. Pubmed ID: 34438161; DOI: 10.1016/j.scr.2021.102509 XACHi012-AXACHi013-AXACHi014-AXACHi015-A 2021-10-00 2021-10-00 PubMed: 34438161 DOI: 10.1016/j.scr.2021.102509Associated cell lines:
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Chen K, Zhuang Z, Wang Q, Li K, Xu S, Liu M, Zhang K, Wei L, Zhang Y, Lian H, Zhang B, Zhong C
Establishment of TUSMi009-A, an induced pluripotent stem cell (iPSC) line from a 24-year-old Chinese Han patient with gliocytoma
Chen K et al. Establishment of TUSMi009-A, an induced pluripotent stem cell (iPSC) line from a 24-year-old Chinese Han patient with gliocytoma. . 2021-10-00. Pubmed ID: 34587579; DOI: 10.1016/j.scr.2021.102546 TUSMi009-A 2021-10-00 2021-10-00 PubMed: 34587579 DOI: 10.1016/j.scr.2021.102546Associated cell lines:
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Lu X, Song N, Wang W, Liu Y, Song H, Xu L, Wang Y, Wei C, Chen J, Yang X, Han F
Generation of integration-free human iPSC line LCPHi001-A from a Parkinson's disease patient carrying the RecNciI mutation in GBA gene
Lu X et al. Generation of integration-free human iPSC line LCPHi001-A from a Parkinson's disease patient carrying the RecNciI mutation in GBA gene. . 2021-10-00. Pubmed ID: 34464855; DOI: 10.1016/j.scr.2021.102514 LCPHi001-A 2021-10-00 2021-10-00 PubMed: 34464855 DOI: 10.1016/j.scr.2021.102514Associated cell lines:
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Leeson HC, Hunter Z, Chaggar HK, Mackay-Sim A, Wolvetang EJ
Reprogramming of human olfactory neurosphere-derived cells from olfactory mucosal biopsies of a control cohort
Leeson HC et al. Reprogramming of human olfactory neurosphere-derived cells from olfactory mucosal biopsies of a control cohort. . 2021-10-00. Pubmed ID: 34507143; DOI: 10.1016/j.scr.2021.102527 AIBNi013-A 2021-10-00 2021-10-00 PubMed: 34507143 DOI: 10.1016/j.scr.2021.102527Associated cell lines:
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Shao J, Shao C, Jin Y, Wang X, Fan H, Yang G
Non-integrating episomal vectors induced pluripotent stem cell line (SDPHi001-A) from a healthy female individual
Shao J et al. Non-integrating episomal vectors induced pluripotent stem cell line (SDPHi001-A) from a healthy female individual. . 2021-10-00. Pubmed ID: 34547706; DOI: 10.1016/j.scr.2021.102540 SDQLCHi025-A 2021-10-00 2021-10-00 PubMed: 34547706 DOI: 10.1016/j.scr.2021.102540Associated cell lines:
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Akter M, Cui H, Chen YH, Ding B
Generation of two induced pluripotent stem cell lines with heterozygous and homozygous GAG deletion in TOR1A gene from a healthy hiPSC line
Akter M et al. Generation of two induced pluripotent stem cell lines with heterozygous and homozygous GAG deletion in TOR1A gene from a healthy hiPSC line. . 2021-10-00. Pubmed ID: 34536661; DOI: 10.1016/j.scr.2021.102536; PMC: PMC8561712 UCSFi001-AUCSFi001-A-49UCSFi001-A-50UCSFi001-A-51 2021-10-00 2021-10-00 PubMed: 34536661 DOI: 10.1016/j.scr.2021.102536Associated cell lines:
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Daoutsali E, Hailu TT, Buijsen RAM, Pepers BA, van der Graaf LM, Verbeek MM, Curtis D, de Vlaam T, van Roon-Mom WMC
Antisense Oligonucleotide-Induced Amyloid Precursor Protein Splicing Modulation as a Therapeutic Approach for Dutch-Type Cerebral Amyloid Angiopathy
Daoutsali E et al. Antisense Oligonucleotide-Induced Amyloid Precursor Protein Splicing Modulation as a Therapeutic Approach for Dutch-Type Cerebral Amyloid Angiopathy. . 2021-10-00. Pubmed ID: 34061681; DOI: 10.1089/nat.2021.0005; PMC: PMC8823675 LUMCi005-A 2021-10-00 2021-10-00 PubMed: 34061681 DOI: 10.1089/nat.2021.0005Associated cell lines:
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Fan T, He J, Wang Y, Yu J, Sun W
Generation of an induced pluripotent stem cell line (FDCHi006-A) from a 7-year-old girl with central precocious puberty
Fan T et al. Generation of an induced pluripotent stem cell line (FDCHi006-A) from a 7-year-old girl with central precocious puberty. . 2021-10-00. Pubmed ID: 34619645; DOI: 10.1016/j.scr.2021.102542 FDCHi006-A 2021-10-00 2021-10-00 PubMed: 34619645 DOI: 10.1016/j.scr.2021.102542Associated cell lines:
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Song Y, Liu J, Li J, Ou Z, Liang D, Chen X, Tang T, Xing P, Guo L, Ye Q, Chen X, Li W, Chen Y, Wang X
Generation and characterization of a human iPSC line HECi001-A from a healthy adult donor pancreata
Song Y et al. Generation and characterization of a human iPSC line HECi001-A from a healthy adult donor pancreata. . 2021-10-00. Pubmed ID: 34600296; DOI: 10.1016/j.scr.2021.102541 HECi001-A 2021-10-00 2021-10-00 PubMed: 34600296 DOI: 10.1016/j.scr.2021.102541Associated cell lines:
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Ben-Haim Y, Armon L, Fichtman B, Epshtein I, Spiegel R, Harel A, Urbach A
Generation and characterization of iPSC lines from two nuclear envelopathy patients with a homozygous nonsense mutation in the TOR1AIP1 gene
Ben-Haim Y et al. Generation and characterization of iPSC lines from two nuclear envelopathy patients with a homozygous nonsense mutation in the TOR1AIP1 gene. . 2021-10-00. Pubmed ID: 34560421; DOI: 10.1016/j.scr.2021.102539 BIUi001-ABIUi002-A 2021-10-00 2021-10-00 PubMed: 34560421 DOI: 10.1016/j.scr.2021.102539 -
Hunter ZL, Leeson HC, Shaker MR, Wolvetang EJ, Vadlamudi L
Generation of induced pluripotent stem cell lines from peripheral blood mononuclear cells of three drug resistant and three drug responsive epilepsy patients
Hunter ZL et al. Generation of induced pluripotent stem cell lines from peripheral blood mononuclear cells of three drug resistant and three drug responsive epilepsy patients. . 2021-10-00. Pubmed ID: 34649201; DOI: 10.1016/j.scr.2021.102564 AIBNi001-AAIBNi002-AAIBNi003-AAIBNi004-AAIBNi005-AAIBNi006-A 2021-10-00 2021-10-00 PubMed: 34649201 DOI: 10.1016/j.scr.2021.102564Associated cell lines:
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Jelinkova S, Martyniak A, Dulak J, Stępniewski J
Derivation of human pluripotent stem cell line via CRISPR/Cas9 mediated deletion of exon 3 LAMA2 gene (DMBi001-A-1)
Jelinkova S et al. Derivation of human pluripotent stem cell line via CRISPR/Cas9 mediated deletion of exon 3 LAMA2 gene (DMBi001-A-1). . 2021-10-00. Pubmed ID: 34509921; DOI: 10.1016/j.scr.2021.102529 DMBi001-ADMBi001-A-1 2021-10-00 2021-10-00 PubMed: 34509921 DOI: 10.1016/j.scr.2021.102529Associated cell lines:
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Zhang Q, Wang Z, Sun H, Chen N, Xu X, Yang J, Gao Y, Wang Y, Xu Y
Generation of induced pluripotent stem cell line (ZZUi030-A) from a patient with spastic paraplegia type 7
Zhang Q et al. Generation of induced pluripotent stem cell line (ZZUi030-A) from a patient with spastic paraplegia type 7. . 2021-10-00. Pubmed ID: 34509920; DOI: 10.1016/j.scr.2021.102525 ZZUi030-A 2021-10-00 2021-10-00 PubMed: 34509920 DOI: 10.1016/j.scr.2021.102525Associated cell lines:
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Liu M, Ge N, Zhang J, Yang M, Yang F, Krawczyk J, Ward D, McInerney V, O'Brien T, Shen S, Prendiville T
Derivation and characterization of two human induced pluripotent stem cell lines (NUIGi004-A) and (NUIGi012-A) from two patients with LQT2 disease
Liu M et al. Derivation and characterization of two human induced pluripotent stem cell lines (NUIGi004-A) and (NUIGi012-A) from two patients with LQT2 disease. . 2021-10-00. Pubmed ID: 34628246; DOI: 10.1016/j.scr.2021.102555 NUIGi004-ANUIGi012-A 2021-10-00 2021-10-00 PubMed: 34628246 DOI: 10.1016/j.scr.2021.102555Associated cell lines:
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Wu H, Wang G, Gao E, Zhang L, Zhu Y, Zhang J, Liu Z
Generation of the induced pluripotent stem cell line (NCKDi004-A) from a 17-year-old patient with Alport syndrome carrying a homozygous mutation in COL4A3 gene
Wu H et al. Generation of the induced pluripotent stem cell line (NCKDi004-A) from a 17-year-old patient with Alport syndrome carrying a homozygous mutation in COL4A3 gene. . 2021-10-00. Pubmed ID: 34626894; DOI: 10.1016/j.scr.2021.102557 NCKDi004-A 2021-10-00 2021-10-00 PubMed: 34626894 DOI: 10.1016/j.scr.2021.102557Associated cell lines:
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Ziegler GC, Radtke F, Vitale MR, Preuße A, Klopocki E, Herms S, Lesch KP
Generation of multiple human iPSC lines from peripheral blood mononuclear cells of two SLC2A3 deletion and two SLC2A3 duplication carriers
Ziegler GC et al. Generation of multiple human iPSC lines from peripheral blood mononuclear cells of two SLC2A3 deletion and two SLC2A3 duplication carriers. . 2021-10-00. Pubmed ID: 34492570; DOI: 10.1016/j.scr.2021.102526 UKWMPi007-AUKWMPi007-BUKWMPi008-AUKWMPi008-BUKWMPi011-AUKWMPi011-BUKWMPi012-AUKWMPi012-B 2021-10-00 2021-10-00 PubMed: 34492570 DOI: 10.1016/j.scr.2021.102526Associated cell lines:
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Lee Y, Park H, Kyung Koo S, Kim JH
Establishment of a human induced pluripotent stem cell line, KSCBi015-A, from a long QT syndrome type 1 patient harboring a KCNQ1 mutation
Lee Y et al. Establishment of a human induced pluripotent stem cell line, KSCBi015-A, from a long QT syndrome type 1 patient harboring a KCNQ1 mutation. . 2021-10-00. Pubmed ID: 34509919; DOI: 10.1016/j.scr.2021.102521 KSCBi005-AKSCBi005-A-1KSCBi015-A 2021-10-00 2021-10-00 PubMed: 34509919 DOI: 10.1016/j.scr.2021.102521Associated cell lines:
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Hu L, Wang G, Wu H, Fu H, Wang Y, Yu F, Liu Z, Mao J
Establishment of an induced pluripotent stem cell line (NCKDi003-A) from a patient with X-linked Dent disease (X-Dent) carrying the hemizygote mutation p. T277P (c. 829A > C) in the CLCN5 gene
Hu L et al. Establishment of an induced pluripotent stem cell line (NCKDi003-A) from a patient with X-linked Dent disease (X-Dent) carrying the hemizygote mutation p. T277P (c. 829A > C) in the CLCN5 gene. . 2021-10-00. Pubmed ID: 34547705; DOI: 10.1016/j.scr.2021.102538 NCKDi003-A 2021-10-00 2021-10-00 PubMed: 34547705 DOI: 10.1016/j.scr.2021.102538Associated cell lines:
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Schoger E, Zimmermann WH, Cyganek L, Zelarayán LC
Establishment of a second generation homozygous CRISPRa human induced pluripotent stem cell (hiPSC) line for enhanced levels of endogenous gene activation
Schoger E et al. Establishment of a second generation homozygous CRISPRa human induced pluripotent stem cell (hiPSC) line for enhanced levels of endogenous gene activation. . 2021-10-00. Pubmed ID: 34481190; DOI: 10.1016/j.scr.2021.102518 RUCDRi002-A-15 2021-10-00 2021-10-00 PubMed: 34481190 DOI: 10.1016/j.scr.2021.102518Associated cell lines:
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Leeson HC, Hunter Z, Chaggar HK, Lavin MF, Mackay-Sim A, Wolvetang EJ
Ataxia Telangiectasia iPSC line generated from a patient olfactory biopsy identifies novel disease-causing mutations
Leeson HC et al. Ataxia Telangiectasia iPSC line generated from a patient olfactory biopsy identifies novel disease-causing mutations. . 2021-10-00. Pubmed ID: 34507142; DOI: 10.1016/j.scr.2021.102528 AIBNi014-A 2021-10-00 2021-10-00 PubMed: 34507142 DOI: 10.1016/j.scr.2021.102528Associated cell lines:
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Elsayed AK, Salloum-Asfar S, Abdulla SA
Human induced pluripotent stem cell line (QBRIi013-A) derivation from a 6-year-old female diagnosed with Autism spectrum disorder (ASD) and intellectual disability (ID)
Elsayed AK et al. Human induced pluripotent stem cell line (QBRIi013-A) derivation from a 6-year-old female diagnosed with Autism spectrum disorder (ASD) and intellectual disability (ID). . 2021-10-00. Pubmed ID: 34438163; DOI: 10.1016/j.scr.2021.102500 QBRIi013-A 2021-10-00 2021-10-00 PubMed: 34438163 DOI: 10.1016/j.scr.2021.102500Associated cell lines:
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Lu JZ, Qiao ZB, Zhang L, Cao HX, Bai ZH, Qi YY, Zhu HY, Chen YQ, Zhang SM, Yan XH, Bao Y, Jia WW, Liu ZM
Generation of a laminopathies-specific iPSC line EHTJUi005-A-3 with homozygous knockout of the LMNA gene by CRISPR/Cas9 technology
Lu JZ et al. Generation of a laminopathies-specific iPSC line EHTJUi005-A-3 with homozygous knockout of the LMNA gene by CRISPR/Cas9 technology. . 2021-10-00. Pubmed ID: 34507144; DOI: 10.1016/j.scr.2021.102530 EHTJUi005-AEHTJUi005-A-3 2021-10-00 2021-10-00 PubMed: 34507144 DOI: 10.1016/j.scr.2021.102530Associated cell lines:
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Oh J, Lee SH, Choi J, Choi JR, Kim S, Cha YJ, Choi HK, Won D, Yoon HG, Park SW, Kang SM, Lee ST, Lee SH
Establishment of a novel human iPSC line (YCMi003-A) from a patient with dilated cardiomyopathy carrying genetic variant LMNA p.Asp364His
Oh J et al. Establishment of a novel human iPSC line (YCMi003-A) from a patient with dilated cardiomyopathy carrying genetic variant LMNA p.Asp364His. . 2021-10-00. Pubmed ID: 34438160; DOI: 10.1016/j.scr.2021.102508 YCMi003-A 2021-10-00 2021-10-00 PubMed: 34438160 DOI: 10.1016/j.scr.2021.102508Associated cell lines:
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Qiao ZB, Lu JZ, Zhang L, Cao HX, Bai ZH, Qi YY, Zhu HY, Zhang SM, Bao Y, Jia WW, Liu ZM
CRISPR/Cas9 mediated generation of a iPSC line EHTJUi005-A-1 with homozygous knockout of the SUV39H1 gene
Qiao ZB et al. CRISPR/Cas9 mediated generation of a iPSC line EHTJUi005-A-1 with homozygous knockout of the SUV39H1 gene. . 2021-10-00. Pubmed ID: 34464854; DOI: 10.1016/j.scr.2021.102519 EHTJUi005-AEHTJUi005-A-1 2021-10-00 2021-10-00 PubMed: 34464854 DOI: 10.1016/j.scr.2021.102519Associated cell lines:
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Barndt RJ, Ma N, Tang Y, Haugh MP, Alamri LS, Chan SY, Wu H
Modeling of dilated cardiomyopathy by establishment of isogenic human iPSC lines carrying phospholamban C25T (R9C) mutation (UPITTi002-A-1) using CRISPR/Cas9 editing
Barndt RJ et al. Modeling of dilated cardiomyopathy by establishment of isogenic human iPSC lines carrying phospholamban C25T (R9C) mutation (UPITTi002-A-1) using CRISPR/Cas9 editing. . 2021-10-00. Pubmed ID: 34583280; DOI: 10.1016/j.scr.2021.102544; PMC: PMC9699793 UPITTi002-AUPITTi002-A-1 2021-10-00 2021-10-00 PubMed: 34583280 DOI: 10.1016/j.scr.2021.102544Associated cell lines:
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Li T, Ma B, Yang H, Zhu G, Shu C, Luo M, Zhou Z
Generation of a CRISPR/Cas9-corrected-hiPSC (NCCDFWi001-A-1) from a Marfan syndrome patient hiPSC with a heterozygous c.2613A>C variant in the fibrillin 1 (FBN1) gene
Li T et al. Generation of a CRISPR/Cas9-corrected-hiPSC (NCCDFWi001-A-1) from a Marfan syndrome patient hiPSC with a heterozygous c.2613A>C variant in the fibrillin 1 (FBN1) gene. . 2021-10-00. Pubmed ID: 34592602; DOI: 10.1016/j.scr.2021.102543 NCCDFWi001-ANCCDFWi001-A-1 2021-10-00 2021-10-00 PubMed: 34592602 DOI: 10.1016/j.scr.2021.102543Associated cell lines:
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Thongsin N, Wattanapanitch M
Generation of B2M bi-allelic knockout human induced pluripotent stem cells (MUSIi001-A-1) using a CRISPR/Cas9 system
Thongsin N et al. Generation of B2M bi-allelic knockout human induced pluripotent stem cells (MUSIi001-A-1) using a CRISPR/Cas9 system. . 2021-10-00. Pubmed ID: 34628247; DOI: 10.1016/j.scr.2021.102551 MUSIi001-AMUSIi001-A-1 2021-10-00 2021-10-00 PubMed: 34628247 DOI: 10.1016/j.scr.2021.102551Associated cell lines:
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Zu B, Zhang X, You G, Fu Q
Generation of a homozygous CRISPR/Cas9-mediated knockout human iPSC line for PTCH1 gene
Zu B et al. Generation of a homozygous CRISPR/Cas9-mediated knockout human iPSC line for PTCH1 gene. . 2021-10-00. Pubmed ID: 34509918; DOI: 10.1016/j.scr.2021.102517 SCMCi001-ASCMCi001-A-1 2021-10-00 2021-10-00 PubMed: 34509918 DOI: 10.1016/j.scr.2021.102517Associated cell lines:
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You J, Xi H, Ma S, Yang XJ, Chen L
Generation of a homozygous LRPAP1 knockout human embryonic stem cell line (FDCHDPe009-B) by CRISPR/Cas9 system
You J et al. Generation of a homozygous LRPAP1 knockout human embryonic stem cell line (FDCHDPe009-B) by CRISPR/Cas9 system. . 2021-10-00. Pubmed ID: 34469777; DOI: 10.1016/j.scr.2021.102516 WAe009-A-56WAe009-A-L 2021-10-00 2021-10-00 PubMed: 34469777 DOI: 10.1016/j.scr.2021.102516Associated cell lines:
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Zhou Z, Yoshimatsu S, Qian E, Ishikawa M, Sato T, Ohtaka M, Nakanishi M, Okano H
Generation of a control human induced pluripotent stem cell line using the defective and persistent Sendai virus vector system
Zhou Z et al. Generation of a control human induced pluripotent stem cell line using the defective and persistent Sendai virus vector system. . 2021-10-00. Pubmed ID: 34598113; DOI: 10.1016/j.scr.2021.102549 KEIOi002-A 2021-10-00 2021-10-00 PubMed: 34598113 DOI: 10.1016/j.scr.2021.102549Associated cell lines:
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Lilianty J, Bateman JF, Lamandé SR
Generation of a heterozygous COL2A1 (p.G1113C) hypochondrogenesis mutation iPSC line, MCRIi019-A-7, using CRISPR/Cas9 gene editing
Lilianty J et al. Generation of a heterozygous COL2A1 (p.G1113C) hypochondrogenesis mutation iPSC line, MCRIi019-A-7, using CRISPR/Cas9 gene editing. . 2021-10-00. Pubmed ID: 34543885; DOI: 10.1016/j.scr.2021.102515 MCRIi019-AMCRIi019-A-2MCRIi019-A-7 2021-10-00 2021-10-00 PubMed: 34543885 DOI: 10.1016/j.scr.2021.102515Associated cell lines:
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Labonne T, Elefanty AG, Stanley EG, Schiesser JV
An INSULIN-GFP/GLUCAGON-mCherry reporter line for the study of human pancreatic endocrine cell development
Labonne T et al. An INSULIN-GFP/GLUCAGON-mCherry reporter line for the study of human pancreatic endocrine cell development. . 2021-10-00. Pubmed ID: 34619644; DOI: 10.1016/j.scr.2021.102547 ESIBIe003-A-10 2021-10-00 2021-10-00 PubMed: 34619644 DOI: 10.1016/j.scr.2021.102547Associated cell lines:
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Shan W, An G, Ren Q, Wang Q
Generation of SCN1B knock out induced pluripotent stem cell (iPSC) line (refractory epilepsy syndrome and Brugada syndrome related cell line)
Shan W et al. Generation of SCN1B knock out induced pluripotent stem cell (iPSC) line (refractory epilepsy syndrome and Brugada syndrome related cell line). . 2021-10-00. Pubmed ID: 34583279; DOI: 10.1016/j.scr.2021.102545 BJTTHi001-ABJTTHi001-A-2 2021-10-00 2021-10-00 PubMed: 34583279 DOI: 10.1016/j.scr.2021.102545Associated cell lines:
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Qin Z, Sun L, Sun X, Su H, Gao X
A CRISPR/Cas9 strategy for the generation of a FLNC knockout hESC line (WAe009-A-70) to model dilated cardiomyopathy and arrhythmogenic right ventricular cardiomyopathy
Qin Z et al. A CRISPR/Cas9 strategy for the generation of a FLNC knockout hESC line (WAe009-A-70) to model dilated cardiomyopathy and arrhythmogenic right ventricular cardiomyopathy. . 2021-10-00. Pubmed ID: 34634758; DOI: 10.1016/j.scr.2021.102562 WAe009-AWAe009-A-70 2021-10-00 2021-10-00 PubMed: 34634758 DOI: 10.1016/j.scr.2021.102562Associated cell lines:
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Ahmed E, Fieldes M, Mianné J, Bourguignon C, Nasri A, Vachier I, Assou S, Bourdin A, De Vos J
Generation of four severe early-onset chronic obstructive pulmonary disease (COPD) patient-derived induced pluripotent stem cell lines from peripheral blood mononuclear cells
Ahmed E et al. Generation of four severe early-onset chronic obstructive pulmonary disease (COPD) patient-derived induced pluripotent stem cell lines from peripheral blood mononuclear cells. . 2021-10-00. Pubmed ID: 34624616; DOI: 10.1016/j.scr.2021.102550 UHOMi002-AUHOMi003-AUHOMi004-AUHOMi005-AUHOMi006-A 2021-10-00 2021-10-00 PubMed: 34624616 DOI: 10.1016/j.scr.2021.102550Associated cell lines:
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Pavlinov I, Farkhondeh A, Yang S, Xu M, Cheng YS, Beers J, Zou J, Liu C, Might M, Rodems S, Baumgärtel K, Zheng W
Generation of two gene corrected human isogenic iPSC lines (NCATS-CL6104 and NCATS-CL6105) from a patient line (NCATS-CL6103) carrying a homozygous p.R401X mutation in the NGLY1 gene using CRISPR/Cas9
Pavlinov I et al. Generation of two gene corrected human isogenic iPSC lines (NCATS-CL6104 and NCATS-CL6105) from a patient line (NCATS-CL6103) carrying a homozygous p.R401X mutation in the NGLY1 gene using CRISPR/Cas9. . 2021-10-00. Pubmed ID: 34619643; DOI: 10.1016/j.scr.2021.102554; PMC: PMC8647947 TRNDi010-CTRNDi021-CTRNDi023-DTRNDi024-DTRNDi025-ATRNDi010-DTRNDi010-D-1TRNDi010-D-2 2021-10-00 2021-10-00 PubMed: 34619643 DOI: 10.1016/j.scr.2021.102554Associated cell lines:
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Schinke C, Fernandez Vallone V, Ivanov A, Peng Y, Körtvelyessy P, Nolte L, Huehnchen P, Beule D, Stachelscheid H, Boehmerle W, Endres M
Dataset for: Modeling chemotherapy induced neurotoxicity with human induced pluripotent stem cell (iPSC)-derived sensory neurons
Schinke C et al. Dataset for: Modeling chemotherapy induced neurotoxicity with human induced pluripotent stem cell (iPSC)-derived sensory neurons. . 2021-10-00. Pubmed ID: 34485650; DOI: 10.1016/j.dib.2021.107320; PMC: PMC8408513 BIHi002-ABIHi005-ABIHi004-B 2021-10-00 2021-10-00 PubMed: 34485650 DOI: 10.1016/j.dib.2021.107320 -
Liu N, Yang X, Yang L, Xu J, Dong R, Li Y, Li Z, Zhang H, Gao M, Lv Y, Liu Y, Gai Z
Establishment of human induced pluripotent stem cell line (SDQLCHi040-A) from a patient with Infantile-onset inflammatory bowel disease carrying a homozygous mutation in IL10RA gene
Liu N et al. Establishment of human induced pluripotent stem cell line (SDQLCHi040-A) from a patient with Infantile-onset inflammatory bowel disease carrying a homozygous mutation in IL10RA gene. . 2021-10-00. Pubmed ID: 34530396; DOI: 10.1016/j.scr.2021.102533 SDQLCHi040-A 2021-10-00 2021-10-00 PubMed: 34530396 DOI: 10.1016/j.scr.2021.102533Associated cell lines:
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Liu A, Jin M, Xie L, Jing M, Zhou Y, Tang M, Lin T, Wang D
Loss of miR-29a impairs decidualization of endometrial stromal cells by TET3 mediated demethylation of Col1A1 promoter
Liu A et al. Loss of miR-29a impairs decidualization of endometrial stromal cells by TET3 mediated demethylation of Col1A1 promoter. . 2021-09-24. Pubmed ID: 34568789; DOI: 10.1016/j.isci.2021.103065; PMC: PMC8449092 KSCBi006-A 2021-09-24 2021-09-24 PubMed: 34568789 DOI: 10.1016/j.isci.2021.103065Associated cell lines:
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Ayagama T, Bose SJ, Capel RA, Priestman DA, Berridge G, Fischer R, Galione A, Platt FM, Kramer H, Burton RAB
A modified density gradient proteomic-based method to analyze endolysosomal proteins in cardiac tissue
Ayagama T et al. A modified density gradient proteomic-based method to analyze endolysosomal proteins in cardiac tissue. . 2021-09-24. Pubmed ID: 34466782; DOI: 10.1016/j.isci.2021.102949; PMC: PMC8384914 CRMi001-ACRMi001-A-1 2021-09-24 2021-09-24 PubMed: 34466782 DOI: 10.1016/j.isci.2021.102949Associated cell lines:
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Koval Hanna, Lutsenko Olena, Bondarovych Mykola, Ostankov Maksym, Goltsev Anatoliy
The Role of Cord Blood in the Regulation of the Cellular and Humoral Link of Immunity in Experimental Atopic Dermatitis
Koval Hanna et al. The Role of Cord Blood in the Regulation of the Cellular and Humoral Link of Immunity in Experimental Atopic Dermatitis. . 2021-09-22. DOI: 10.20535/ibb.2021.5.3.238976 MUSIi013-A 2021-09-22 2021-09-22 DOI: 10.20535/ibb.2021.5.3.238976Associated cell lines:
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Kidwai FK, Mui BWH, Almpani K, Jani P, Keyvanfar C, Iqbal K, Paravastu SS, Arora D, Orzechowski P, Merling RK, Mallon B, Myneni VD, Ahmad M, Kruszka P, Muenke M, Woodcock J, Gilman JW, Robey PG, Lee JS
Quantitative Craniofacial Analysis and Generation of Human Induced Pluripotent Stem Cells for Muenke Syndrome: A Case Report
Kidwai FK et al. Quantitative Craniofacial Analysis and Generation of Human Induced Pluripotent Stem Cells for Muenke Syndrome: A Case Report. . 2021-09-22. Pubmed ID: 34698187; DOI: 10.3390/jdb9040039; PMC: PMC8544470 CRMi001-ANIDCRi001-A 2021-09-22 2021-09-22 PubMed: 34698187 DOI: 10.3390/jdb9040039Associated cell lines:
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Dolde X, Karreman C, Wiechers M, Schildknecht S, Leist M
Profiling of Human Neural Crest Chemoattractant Activity as a Replacement of Fetal Bovine Serum for In Vitro Chemotaxis Assays
Dolde X et al. Profiling of Human Neural Crest Chemoattractant Activity as a Replacement of Fetal Bovine Serum for In Vitro Chemotaxis Assays. . 2021-09-18. Pubmed ID: 34576243; DOI: 10.3390/ijms221810079; PMC: PMC8468192 SIGi001-A 2021-09-18 2021-09-18 PubMed: 34576243 DOI: 10.3390/ijms221810079Associated cell lines:
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He L, Wang S, Peng L, Zhao H, Li S, Han X, Habimana JD, Chen Z, Wang C, Peng Y, Peng H, Xie Y, Lei L, Deng Q, Wan L, Wan N, Yuan H, Gong Y, Zou G, Li Z, Tang B, Jiang H
CRISPR/Cas9 mediated gene correction ameliorates abnormal phenotypes in spinocerebellar ataxia type 3 patient-derived induced pluripotent stem cells
He L et al. CRISPR/Cas9 mediated gene correction ameliorates abnormal phenotypes in spinocerebellar ataxia type 3 patient-derived induced pluripotent stem cells. . 2021-09-17. Pubmed ID: 34535635; DOI: 10.1038/s41398-021-01605-2; PMC: PMC8448778 CSUXHi001-ACSUXHi002-ACSUXHi005-A 2021-09-17 2021-09-17 PubMed: 34535635 DOI: 10.1038/s41398-021-01605-2Associated cell lines:
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Scaramuzzino L, Lucchino V, Scalise S, Lo Conte M, Zannino C, Sacco A, Biamonte F, Parrotta EI, Costanzo FS, Cuda G
Uncovering the Metabolic and Stress Responses of Human Embryonic Stem Cells to FTH1 Gene Silencing
Scaramuzzino L et al. Uncovering the Metabolic and Stress Responses of Human Embryonic Stem Cells to FTH1 Gene Silencing. . 2021-09-15. Pubmed ID: 34572080; DOI: 10.3390/cells10092431; PMC: PMC8469604 UNIMGi003-AUNIMGi004-A 2021-09-15 2021-09-15 PubMed: 34572080 DOI: 10.3390/cells10092431Associated cell lines:
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Imbrici P, Conte E, Blunck R, Stregapede F, Liantonio A, Tosi M, D'Adamo MC, De Luca A, Brankovic V, Zanni G
A Novel KCNA2 Variant in a Patient with Non-Progressive Congenital Ataxia and Epilepsy: Functional Characterization and Sensitivity to 4-Aminopyridine
Imbrici P et al. A Novel KCNA2 Variant in a Patient with Non-Progressive Congenital Ataxia and Epilepsy: Functional Characterization and Sensitivity to 4-Aminopyridine. . 2021-09-14. Pubmed ID: 34576077; DOI: 10.3390/ijms22189913; PMC: PMC8469797 HIHDNEi002-AHIHDNEi003-A 2021-09-14 2021-09-14 PubMed: 34576077 DOI: 10.3390/ijms22189913Associated cell lines:
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Diao X, Wang F, Becerra-Calixto A, Soto C, Mukherjee A
Induced Pluripotent Stem Cell-Derived Dopaminergic Neurons from Familial Parkinson's Disease Patients Display α-Synuclein Pathology and Abnormal Mitochondrial Morphology
Diao X et al. Induced Pluripotent Stem Cell-Derived Dopaminergic Neurons from Familial Parkinson's Disease Patients Display α-Synuclein Pathology and Abnormal Mitochondrial Morphology. . 2021-09-13. Pubmed ID: 34572052; DOI: 10.3390/cells10092402; PMC: PMC8467069 BCMi001-A 2021-09-13 2021-09-13 PubMed: 34572052 DOI: 10.3390/cells10092402Associated cell lines:
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Lim ZR, Vassilev S, Leong YW, Hang JW, Rénia L, Malleret B, Oh SK
Industrially Compatible Transfusable iPSC-Derived RBCs: Progress, Challenges and Prospective Solutions
Lim ZR et al. Industrially Compatible Transfusable iPSC-Derived RBCs: Progress, Challenges and Prospective Solutions. . 2021-09-10. Pubmed ID: 34575977; DOI: 10.3390/ijms22189808; PMC: PMC8472628 KRIBBi001-A 2021-09-10 2021-09-10 PubMed: 34575977 DOI: 10.3390/ijms22189808Associated cell lines:
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Sommariva E, Stadiotti I, Casella M, Catto V, Dello Russo A, Carbucicchio C, Arnaboldi L, De Metrio S, Milano G, Scopece A, Casaburo M, Andreini D, Mushtaq S, Conte E, Chiesa M, Birchmeier W, Cogliati E, Paolin A, König E, Meraviglia V, De Musso M, Volani C, Cattelan G, Rauhe W, Turnu L, Porro B, Pedrazzini M, Camera M, Corsini A, Tondo C, Rossini A, Pompilio G
Oxidized LDL-dependent pathway as new pathogenic trigger in arrhythmogenic cardiomyopathy
Sommariva E et al. Oxidized LDL-dependent pathway as new pathogenic trigger in arrhythmogenic cardiomyopathy. . 2021-09-07. Pubmed ID: 34337880; DOI: 10.15252/emmm.202114365; PMC: PMC8422076 EURACi001-AEURACi002-AEURACi003-AEURACi004-A 2021-09-07 2021-09-07 PubMed: 34337880 DOI: 10.15252/emmm.202114365Associated cell lines:
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Salmina AB, Kapkaeva MR, Vetchinova AS, Illarioshkin SN
Novel Approaches Used to Examine and Control Neurogenesis in Parkinson's Disease
Salmina AB et al. Novel Approaches Used to Examine and Control Neurogenesis in Parkinson's Disease. . 2021-09-04. Pubmed ID: 34502516; DOI: 10.3390/ijms22179608; PMC: PMC8431772 RCPCMi004-A 2021-09-04 2021-09-04 PubMed: 34502516 DOI: 10.3390/ijms22179608Associated cell lines:
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Yue W.
Heterozygous living donor liver transplantation for pediatric maple syrup urine disease with new compound mutation of BCKDHB gene: a case report and literature review
Yue W.. Heterozygous living donor liver transplantation for pediatric maple syrup urine disease with new compound mutation of BCKDHB gene: a case report and literature review. . 2021-09-01. DOI: 10.3969/j.issn.1674-7445.2021.05.013 SDQLCHi006-A 2021-09-01 2021-09-01 DOI: 10.3969/j.issn.1674-7445.2021.05.013Associated cell lines:
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de Jong JO, Llapashtica C, Genestine M, Strauss K, Provenzano F, Sun Y, Zhu H, Cortese GP, Brundu F, Brigatti KW, Corneo B, Migliori B, Tomer R, Kushner SA, Kellendonk C, Javitch JA, Xu B, Markx S
Cortical overgrowth in a preclinical forebrain organoid model of CNTNAP2-associated autism spectrum disorder
de Jong JO et al. Cortical overgrowth in a preclinical forebrain organoid model of CNTNAP2-associated autism spectrum disorder. . 2021-09-01. Pubmed ID: 34471112; DOI: 10.1038/s41467-021-24358-4; PMC: PMC8410758 FRIMOi003-AFRIMOi004-A 2021-09-01 2021-09-01 PubMed: 34471112 DOI: 10.1038/s41467-021-24358-4Associated cell lines:
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Bagheri-Mohammadi S
Stem cell-based therapy as a promising approach in Alzheimer's disease: current perspectives on novel treatment
Bagheri-Mohammadi S. Stem cell-based therapy as a promising approach in Alzheimer's disease: current perspectives on novel treatment. . 2021-09-00. Pubmed ID: 33398492; DOI: 10.1007/s10561-020-09896-3 ZZUi010-A 2021-09-00 2021-09-00 PubMed: 33398492 DOI: 10.1007/s10561-020-09896-3Associated cell lines:
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Wang L, Sievert D, Clark AE, Lee S, Federman H, Gastfriend BD, Shusta EV, Palecek SP, Carlin AF, Gleeson JG
A human three-dimensional neural-perivascular 'assembloid' promotes astrocytic development and enables modeling of SARS-CoV-2 neuropathology
Wang L et al. A human three-dimensional neural-perivascular 'assembloid' promotes astrocytic development and enables modeling of SARS-CoV-2 neuropathology. . 2021-09-00. Pubmed ID: 34244682; DOI: 10.1038/s41591-021-01443-1; PMC: PMC8601037 WAe001-A 2021-09-00 2021-09-00 PubMed: 34244682 DOI: 10.1038/s41591-021-01443-1Associated cell lines:
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Marín-Quílez A, García-Tuñón I, Fernández-Infante C, Hernández-Cano L, Palma-Barqueros V, Vuelta E, Sánchez-Martín M, González-Porras JR, Guerrero C, Benito R, Rivera J, Hernández-Rivas JM, Bastida JM
Characterization of the Platelet Phenotype Caused by a Germline RUNX1 Variant in a CRISPR/Cas9-Generated Murine Model
Marín-Quílez A et al. Characterization of the Platelet Phenotype Caused by a Germline RUNX1 Variant in a CRISPR/Cas9-Generated Murine Model. . 2021-09-00. Pubmed ID: 33626581; DOI: 10.1055/s-0041-1723987 GENYOi005-A 2021-09-00 2021-09-00 PubMed: 33626581 DOI: 10.1055/s-0041-1723987Associated cell lines:
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Ghori FF, Wahid M
Induced pluripotent stem cells from urine of Duchenne muscular dystrophy patients
Ghori FF et al. Induced pluripotent stem cells from urine of Duchenne muscular dystrophy patients. . 2021-09-00. Pubmed ID: 33599058; DOI: 10.1111/ped.14655 UKWNLi001-A 2021-09-00 2021-09-00 PubMed: 33599058 DOI: 10.1111/ped.14655Associated cell lines:
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Choudhury S, Surendran N, Das A
Recent advances in the induced pluripotent stem cell-based skin regeneration
Choudhury S et al. Recent advances in the induced pluripotent stem cell-based skin regeneration. . 2021-09-00. Pubmed ID: 33970525; DOI: 10.1111/wrr.12925 KCLi001-A 2021-09-00 2021-09-00 PubMed: 33970525 DOI: 10.1111/wrr.12925Associated cell lines:
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Mohana Devi S, Abishek Kumar B, Mahalaxmi I, Balachandar V
Leber's hereditary optic neuropathy: Current approaches and future perspectives on Mesenchymal stem cell-mediated rescue
Mohana Devi S et al. Leber's hereditary optic neuropathy: Current approaches and future perspectives on Mesenchymal stem cell-mediated rescue. . 2021-09-00. Pubmed ID: 34454075; DOI: 10.1016/j.mito.2021.08.013 FINCBi001-A 2021-09-00 2021-09-00 PubMed: 34454075 DOI: 10.1016/j.mito.2021.08.013Associated cell lines:
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Duong Phu M, Bross S, Burkhalter MD, Philipp M
Limitations and opportunities in the pharmacotherapy of ciliopathies
Duong Phu M et al. Limitations and opportunities in the pharmacotherapy of ciliopathies. . 2021-09-00. Pubmed ID: 33771583; DOI: 10.1016/j.pharmthera.2021.107841 MHHi016-AMHHi016-B 2021-09-00 2021-09-00 PubMed: 33771583 DOI: 10.1016/j.pharmthera.2021.107841 -
Wang Y, Yan F, Nasar A, Chen ZS, Altorki NK, Stiles B, Narula N, Zhou P
CUL4(high) Lung Adenocarcinomas Are Dependent on the CUL4-p21 Ubiquitin Signaling for Proliferation and Survival
Wang Y et al. CUL4(high) Lung Adenocarcinomas Are Dependent on the CUL4-p21 Ubiquitin Signaling for Proliferation and Survival. . 2021-09-00. Pubmed ID: 34119472; DOI: 10.1016/j.ajpath.2021.05.018; PMC: PMC8420861 SDUBMSi002-A 2021-09-00 2021-09-00 PubMed: 34119472 DOI: 10.1016/j.ajpath.2021.05.018Associated cell lines:
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Bi XA, Li L, Xu R, Xing Z
Pathogenic Factors Identification of Brain Imaging and Gene in Late Mild Cognitive Impairment
Bi XA et al. Pathogenic Factors Identification of Brain Imaging and Gene in Late Mild Cognitive Impairment. . 2021-09-00. Pubmed ID: 34106420; DOI: 10.1007/s12539-021-00449-0 SIAISi001-A 2021-09-00 2021-09-00 PubMed: 34106420 DOI: 10.1007/s12539-021-00449-0Associated cell lines:
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Aguado J, Chaggar HK, Gómez-Inclán C, Shaker MR, Leeson HC, Mackay-Sim A, Wolvetang EJ
Inhibition of the cGAS-STING pathway ameliorates the premature senescence hallmarks of Ataxia-Telangiectasia brain organoids
Aguado J et al. Inhibition of the cGAS-STING pathway ameliorates the premature senescence hallmarks of Ataxia-Telangiectasia brain organoids. . 2021-09-00. Pubmed ID: 34459078; DOI: 10.1111/acel.13468; PMC: PMC8441292 AIBNi014-A 2021-09-00 2021-09-00 PubMed: 34459078 DOI: 10.1111/acel.13468Associated cell lines:
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Shao Z, Masuho I, Tumber A, Maynes JT, Tavares E, Ali A, Hewson S, Schulze A, Kannu P, Martemyanov KA, Vincent A
Extended Phenotyping and Functional Validation Facilitate Diagnosis of a Complex Patient Harboring Genetic Variants in MCCC1 and GNB5 Causing Overlapping Phenotypes
Shao Z et al. Extended Phenotyping and Functional Validation Facilitate Diagnosis of a Complex Patient Harboring Genetic Variants in MCCC1 and GNB5 Causing Overlapping Phenotypes. . 2021-08-29. Pubmed ID: 34573334; DOI: 10.3390/genes12091352; PMC: PMC8469011 CSSi009-ACSSi010-A 2021-08-29 2021-08-29 PubMed: 34573334 DOI: 10.3390/genes12091352 -
Ziegler GC, Ehlis AC, Weber H, Vitale MR, Zöller JEM, Ku HP, Schiele MA, Kürbitz LI, Romanos M, Pauli P, Kalisch R, Zwanzger P, Domschke K, Fallgatter AJ, Reif A, Lesch KP
A Common CDH13 Variant Is Associated with Low Agreeableness and Neural Responses to Working Memory Tasks in ADHD
Ziegler GC et al. A Common CDH13 Variant Is Associated with Low Agreeableness and Neural Responses to Working Memory Tasks in ADHD. . 2021-08-29. Pubmed ID: 34573337; DOI: 10.3390/genes12091356; PMC: PMC8471784 UKWMPi002-AUKWMPi002-A-1UKWMPi002-A-2 2021-08-29 2021-08-29 PubMed: 34573337 DOI: 10.3390/genes12091356Associated cell lines:
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Kallas D, Lamba A, Roston TM, Arslanova A, Franciosi S, Tibbits GF, Sanatani S
Pediatric Catecholaminergic Polymorphic Ventricular Tachycardia: A Translational Perspective for the Clinician-Scientist
Kallas D et al. Pediatric Catecholaminergic Polymorphic Ventricular Tachycardia: A Translational Perspective for the Clinician-Scientist. . 2021-08-27. Pubmed ID: 34502196; DOI: 10.3390/ijms22179293; PMC: PMC8431429 LUMCi020-ALUMCi021-A 2021-08-27 2021-08-27 PubMed: 34502196 DOI: 10.3390/ijms22179293Associated cell lines:
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Vignier N, Chatzifrangkeskou M, Pinton L, Wioland H, Marais T, Lemaitre M, Le Dour C, Peccate C, Cardoso D, Schmitt A, Wu W, Biferi MG, Naouar N, Macquart C, Beuvin M, Decostre V, Bonne G, Romet-Lemonne G, Worman HJ, Tedesco FS, Jégou A, Muchir A
The non-muscle ADF/cofilin-1 controls sarcomeric actin filament integrity and force production in striated muscle laminopathies
Vignier N et al. The non-muscle ADF/cofilin-1 controls sarcomeric actin filament integrity and force production in striated muscle laminopathies. . 2021-08-24. Pubmed ID: 34433058; DOI: 10.1016/j.celrep.2021.109601; PMC: PMC8411111 UCLi007-A 2021-08-24 2021-08-24 PubMed: 34433058 DOI: 10.1016/j.celrep.2021.109601Associated cell lines:
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Dacus D, Wallace NA
Beta-Genus Human Papillomavirus 8 E6 Destabilizes the Host Genome by Promoting p300 Degradation
Dacus D et al. Beta-Genus Human Papillomavirus 8 E6 Destabilizes the Host Genome by Promoting p300 Degradation. . 2021-08-21. Pubmed ID: 34452526; DOI: 10.3390/v13081662; PMC: PMC8402844 IAIi001-A 2021-08-21 2021-08-21 PubMed: 34452526 DOI: 10.3390/v13081662Associated cell lines:
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Pflaum M, Dahlmann J, Engels L, Naghilouy-Hidaji H, Adam D, Zöllner J, Otto A, Schmeckebier S, Martin U, Haverich A, Olmer R, Wiegmann B
Towards Biohybrid Lung: Induced Pluripotent Stem Cell Derived Endothelial Cells as Clinically Relevant Cell Source for Biologization
Pflaum M et al. Towards Biohybrid Lung: Induced Pluripotent Stem Cell Derived Endothelial Cells as Clinically Relevant Cell Source for Biologization. . 2021-08-19. Pubmed ID: 34442603; DOI: 10.3390/mi12080981; PMC: PMC8401467 MHHi001-AMHHi008-A 2021-08-19 2021-08-19 PubMed: 34442603 DOI: 10.3390/mi12080981 -
Li Wener, Luo Xiaojing, Poetsch Mareike S., Oertel Reinhard, Nichani Kapil, Schneider Martin, Strano Anna, Hasse Marcel, Steiner Robert-Patrick, Cyganek Lukas, Hettwer Karina, Uhlig Steffen, Simon Kirsten, Guan Kaomei, Schubert Mario
Effects of Hydroxychloroquine and Azithromycin on iPSC-derived Cardiomyocytes: Considerations for the Treatment of COVID-19 Patients
Li Wener et al. Effects of Hydroxychloroquine and Azithromycin on iPSC-derived Cardiomyocytes: Considerations for the Treatment of COVID-19 Patients. . 2021-08-19. DOI: 10.1101/2021.08.19.456950 UMGi001-AUMGi005-AUMGi014-CUMGi020-B 2021-08-19 2021-08-19 DOI: 10.1101/2021.08.19.456950 -
Vignon A, Salvador-Prince L, Lehmann S, Perrier V, Torrent J
Deconstructing Alzheimer's Disease: How to Bridge the Gap between Experimental Models and the Human Pathology?
Vignon A et al. Deconstructing Alzheimer's Disease: How to Bridge the Gap between Experimental Models and the Human Pathology?. . 2021-08-16. Pubmed ID: 34445475; DOI: 10.3390/ijms22168769; PMC: PMC8395727 IRMBi001-AIRMBi002-A 2021-08-16 2021-08-16 PubMed: 34445475 DOI: 10.3390/ijms22168769Associated cell lines:
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Lei T, Wang J, Liu Y, Chen P, Zhang Z, Zhang X, Guo W, Wang X, Li Q, Du H
Proteomic profile of human stem cells from dental pulp and periodontal ligament
Lei T et al. Proteomic profile of human stem cells from dental pulp and periodontal ligament. . 2021-08-15. Pubmed ID: 34089896; DOI: 10.1016/j.jprot.2021.104280 CRMi001-ACRMi001-A-1 2021-08-15 2021-08-15 PubMed: 34089896 DOI: 10.1016/j.jprot.2021.104280Associated cell lines:
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Palombo F, Peron C, Caporali L, Iannielli A, Maresca A, Di Meo I, Fiorini C, Segnali A, Sciacca FL, Rizzo A, Levi S, Suomalainen A, Prigione A, Broccoli V, Carelli V, Tiranti V
The relevance of mitochondrial DNA variants fluctuation during reprogramming and neuronal differentiation of human iPSCs
Palombo F et al. The relevance of mitochondrial DNA variants fluctuation during reprogramming and neuronal differentiation of human iPSCs. . 2021-08-10. Pubmed ID: 34329598; DOI: 10.1016/j.stemcr.2021.06.016; PMC: PMC8365099 FINCBi001-A 2021-08-10 2021-08-10 PubMed: 34329598 DOI: 10.1016/j.stemcr.2021.06.016Associated cell lines:
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Miressi Federica, Benslimane Nesrine, Favreau Frédéric, Rassat Marion, Richard Laurence, Bourthoumieu Sylvie, Laroche Cécile, Magy Laurent, Magdelaine Corinne, Sturtz Franck, Lia Anne-Sophie, Faye Pierre-Antoine
GDAP1 Involvement in Mitochondrial Function and Oxidative Stress, Investigated in a Charcot-Marie-Tooth Model of hiPSCs-Derived Motor Neurons
Miressi Federica et al. GDAP1 Involvement in Mitochondrial Function and Oxidative Stress, Investigated in a Charcot-Marie-Tooth Model of hiPSCs-Derived Motor Neurons. . 2021-08-02. DOI: 10.3390/biomedicines9080945 LIMFRi001-A 2021-08-02 2021-08-02 DOI: 10.3390/biomedicines9080945Associated cell lines:
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Calado SM, Bento D, Marques N, Bragança J
Generation and cardiac differentiation of a human induced pluripotent stem cell line UALGi002-A from a female patient with Left-Ventricular Noncompaction Cardiomyopathy
Calado SM et al. Generation and cardiac differentiation of a human induced pluripotent stem cell line UALGi002-A from a female patient with Left-Ventricular Noncompaction Cardiomyopathy. . 2021-08-00. Pubmed ID: 34280889; DOI: 10.1016/j.scr.2021.102462 UALGi001-AUALGi002-A 2021-08-00 2021-08-00 PubMed: 34280889 DOI: 10.1016/j.scr.2021.102462Associated cell lines:
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Schwartz GB, Kubo H, Laronda MM
Generation of two human induced pluripotent stem cell lines from a patient with complete androgen insensitivity syndrome with a hemizygous single nucleotide variant in the androgen receptor (AR) gene
Schwartz GB et al. Generation of two human induced pluripotent stem cell lines from a patient with complete androgen insensitivity syndrome with a hemizygous single nucleotide variant in the androgen receptor (AR) gene. . 2021-08-00. Pubmed ID: 34233262; DOI: 10.1016/j.scr.2021.102441 LCHi001-ALCHi001-B 2021-08-00 2021-08-00 PubMed: 34233262 DOI: 10.1016/j.scr.2021.102441 -
Gong T, Wang H, Huang B, Wang H, Zhang P, Qian J
Corrigendum to "Reprogramming of human peripheral blood mononuclear cells from a patient suffering from recurrent hydatidiform mole to an iPSC line FAHZUi001-A carrying a homozygous p.Gln421Ter mutation in NLRP7 gene" [Stem Cell Res. 53 (2021) 102361]
Gong T et al. Corrigendum to "Reprogramming of human peripheral blood mononuclear cells from a patient suffering from recurrent hydatidiform mole to an iPSC line FAHZUi001-A carrying a homozygous p.Gln421Ter mutation in NLRP7 gene" [Stem Cell Res. 53 (2021) 102361]. . 2021-08-00. Pubmed ID: 34330032; DOI: 10.1016/j.scr.2021.102479 FAHZUi001-A 2021-08-00 2021-08-00 PubMed: 34330032 DOI: 10.1016/j.scr.2021.102479Associated cell lines:
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Tang Y, Ren J, Li CC
Establishment of a GFP::LMNB1 knockin cell line (CSUi002-A-1) from a dystonia patient-specific iPSC by CRISPR/Cas9 editing
Tang Y et al. Establishment of a GFP::LMNB1 knockin cell line (CSUi002-A-1) from a dystonia patient-specific iPSC by CRISPR/Cas9 editing. . 2021-08-00. Pubmed ID: 34438319; DOI: 10.1016/j.scr.2021.102505 CSUi002-ACSUi002-A-1 2021-08-00 2021-08-00 PubMed: 34438319 DOI: 10.1016/j.scr.2021.102505Associated cell lines:
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Clayton JS, Scriba CK, Romero NB, Malfatti E, Saker S, Larmonier T, Nowak KJ, Ravenscroft G, Laing NG, Taylor RL
Generation of two isogenic induced pluripotent stem cell lines from a 10-year-old typical nemaline myopathy patient with a heterozygous dominant c.541G>A (p.Asp179Asn) pathogenic variant in the ACTA1 gene
Clayton JS et al. Generation of two isogenic induced pluripotent stem cell lines from a 10-year-old typical nemaline myopathy patient with a heterozygous dominant c.541G>A (p.Asp179Asn) pathogenic variant in the ACTA1 gene. . 2021-08-00. Pubmed ID: 34388489; DOI: 10.1016/j.scr.2021.102482 HPIi002-AHPIi002-B 2021-08-00 2021-08-00 PubMed: 34388489 DOI: 10.1016/j.scr.2021.102482 -
Kim JH, Kang KW, Lee BH, Park Y, Kim BS
Generation of the induced pluripotent stem cell line KUMi001-A carrying the Philadelphia chromosome from a chronic myeloid leukemia patient
Kim JH et al. Generation of the induced pluripotent stem cell line KUMi001-A carrying the Philadelphia chromosome from a chronic myeloid leukemia patient. . 2021-08-00. Pubmed ID: 34280890; DOI: 10.1016/j.scr.2021.102464 KUMCi001-AKUMCi002-AKUMi001-A 2021-08-00 2021-08-00 PubMed: 34280890 DOI: 10.1016/j.scr.2021.102464Associated cell lines:
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Klaihmon P, Luanpitpong S, Lorthongpanich C, Laowtammathron C, Waeteekul S, Terbto P, Issaragrisil S
Episomal vector reprogramming of human umbilical cord blood natural killer cells to an induced pluripotent stem cell line MUSIi013-A
Klaihmon P et al. Episomal vector reprogramming of human umbilical cord blood natural killer cells to an induced pluripotent stem cell line MUSIi013-A. . 2021-08-00. Pubmed ID: 34311438; DOI: 10.1016/j.scr.2021.102472 MUSIi013-A 2021-08-00 2021-08-00 PubMed: 34311438 DOI: 10.1016/j.scr.2021.102472Associated cell lines:
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Zhu T, Wu S, Sun Z, Wei X, Han X, Zou X, Sui R
Generation of two human induced pluripotent stem cell lines from patients with biallelic USH2A variants
Zhu T et al. Generation of two human induced pluripotent stem cell lines from patients with biallelic USH2A variants. . 2021-08-00. Pubmed ID: 34419747; DOI: 10.1016/j.scr.2021.102502 PUMCHi015-APUMCHi016-A 2021-08-00 2021-08-00 PubMed: 34419747 DOI: 10.1016/j.scr.2021.102502Associated cell lines:
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Castaño J, Romero-Moya D, Richaud-Patin Y, Giorgetti A
Generation of two heterozygous GATA2 CRISPR/Cas9-edited iPSC lines, R398W and R396Q, for modeling GATA2 deficiency
Castaño J et al. Generation of two heterozygous GATA2 CRISPR/Cas9-edited iPSC lines, R398W and R396Q, for modeling GATA2 deficiency. . 2021-08-00. Pubmed ID: 34284273; DOI: 10.1016/j.scr.2021.102445 ESi086-A-1ESi086-A-2 2021-08-00 2021-08-00 PubMed: 34284273 DOI: 10.1016/j.scr.2021.102445Associated cell lines:
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Wang W, Bai R, Song X
Generating dHAND homozygous knockout human embryonic stem cell line (WAe009-A-59) by episomal vector-based CRISPR/Cas9 system
Wang W et al. Generating dHAND homozygous knockout human embryonic stem cell line (WAe009-A-59) by episomal vector-based CRISPR/Cas9 system. . 2021-08-00. Pubmed ID: 34332328; DOI: 10.1016/j.scr.2021.102471 WAe009-AWAe009-A-59 2021-08-00 2021-08-00 PubMed: 34332328 DOI: 10.1016/j.scr.2021.102471Associated cell lines:
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Lee J, Liu Z, Tusing YG, Li C, Westin E, Li W, Zhao R
Generation of inducible pluripotent stem cell lines from Alzheimer's disease patients with APOE e3/e3 genotype
Lee J et al. Generation of inducible pluripotent stem cell lines from Alzheimer's disease patients with APOE e3/e3 genotype. . 2021-08-00. Pubmed ID: 34392011; DOI: 10.1016/j.scr.2021.102498; PMC: PMC8496340 UABi001-AUABi002-A 2021-08-00 2021-08-00 PubMed: 34392011 DOI: 10.1016/j.scr.2021.102498 -
Shan W, Yang X, Ren Q, Wang Q
Generation of SCN1A Knock out induced pluripotent stem cell (iPSC) line
Shan W et al. Generation of SCN1A Knock out induced pluripotent stem cell (iPSC) line. . 2021-08-00. Pubmed ID: 34247112; DOI: 10.1016/j.scr.2021.102452 BJTTHi001-ABJTTHi001-A-1 2021-08-00 2021-08-00 PubMed: 34247112 DOI: 10.1016/j.scr.2021.102452Associated cell lines:
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Schwarz L, Casadei N, Fitzgerald JC
Generation of R272Q, S156A and K572R RHOT1/Miro1 point mutations in iPSCs from a healthy individual using FACS-assisted CRISPR/Cas9 genome editing
Schwarz L et al. Generation of R272Q, S156A and K572R RHOT1/Miro1 point mutations in iPSCs from a healthy individual using FACS-assisted CRISPR/Cas9 genome editing. . 2021-08-00. Pubmed ID: 34359002; DOI: 10.1016/j.scr.2021.102469 HIHTFi001-AHIHTFi001-BHIHTFi001-C 2021-08-00 2021-08-00 PubMed: 34359002 DOI: 10.1016/j.scr.2021.102469Associated cell lines:
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Bogomiakova ME, Sekretova EK, Eremeev AV, Shuvalova LD, Bobrovsky PA, Zerkalenkova EA, Lebedeva OS, Lagarkova MA
Derivation of induced pluripotent stem cells line (RCPCMi007-A-1) with inactivation of the beta-2-microglobulin gene by CRISPR/Cas9 genome editing
Bogomiakova ME et al. Derivation of induced pluripotent stem cells line (RCPCMi007-A-1) with inactivation of the beta-2-microglobulin gene by CRISPR/Cas9 genome editing. . 2021-08-00. Pubmed ID: 34237591; DOI: 10.1016/j.scr.2021.102451 RCPCMi007-ARCPCMi007-A-1 2021-08-00 2021-08-00 PubMed: 34237591 DOI: 10.1016/j.scr.2021.102451Associated cell lines:
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Liu X, Zhang S, Chang Y, Wu F, Bai R
Establishment of a KCNQ1 homozygous knockout human embryonic stem cell line by episomal vector-based CRISPR/Cas9 system
Liu X et al. Establishment of a KCNQ1 homozygous knockout human embryonic stem cell line by episomal vector-based CRISPR/Cas9 system. . 2021-08-00. Pubmed ID: 34343827; DOI: 10.1016/j.scr.2021.102467 WAe009-A-62 2021-08-00 2021-08-00 PubMed: 34343827 DOI: 10.1016/j.scr.2021.102467Associated cell lines:
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Li Y, Zhang Y, Li T, Wang X, Bao W, Huang J, Ma Y, Li S, Wang S, Yang Y, Liu Y, Gao Y, Feng H, Li Y
Generation of three iPSC lines from different types of pediatric acute leukemia patients
Li Y et al. Generation of three iPSC lines from different types of pediatric acute leukemia patients. . 2021-08-00. Pubmed ID: 34298433; DOI: 10.1016/j.scr.2021.102460 SCMCi002-ASCMCi003-ASCMCi004-A 2021-08-00 2021-08-00 PubMed: 34298433 DOI: 10.1016/j.scr.2021.102460Associated cell lines:
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Zhang H, Jahng JWS, Liu Y, Chase AJ, Perez MV, Wu JC
Generation of three induced pluripotent stem cell lines (SCVIi014-A, SCVIi015-A, and SCVIi016-A) from patients with LQT1 caused by heterozygous mutations in the KCNQ1 gene
Zhang H et al. Generation of three induced pluripotent stem cell lines (SCVIi014-A, SCVIi015-A, and SCVIi016-A) from patients with LQT1 caused by heterozygous mutations in the KCNQ1 gene. . 2021-08-00. Pubmed ID: 34411974; DOI: 10.1016/j.scr.2021.102492; PMC: PMC9482789 SCVIi003-ASCVIi004-ASCVIi005-ASCVIi014-ASCVIi015-ASCVIi016-A 2021-08-00 2021-08-00 PubMed: 34411974 DOI: 10.1016/j.scr.2021.102492Associated cell lines:
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Ting CY, Huang CY, Chen HC, Chiu YW, Hsieh PCH, Lee JJ
Generation of induced pluripotent stem cells from a Bardet-Biedl syndrome patient carrying a homologous BBS2 c.534 + 1G > T mutation
Ting CY et al. Generation of induced pluripotent stem cells from a Bardet-Biedl syndrome patient carrying a homologous BBS2 c.534 + 1G > T mutation. . 2021-08-00. Pubmed ID: 34364070; DOI: 10.1016/j.scr.2021.102480 IBMSi021-A 2021-08-00 2021-08-00 PubMed: 34364070 DOI: 10.1016/j.scr.2021.102480Associated cell lines:
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Rössler U, Hennig AF, Stelzer N, Bose S, Kopp J, Søe K, Cyganek L, Zifarelli G, Ali S, von der Hagen M, Strässler ET, Hahn G, Pusch M, Stauber T, Izsvák Z, Gossen M, Stachelscheid H, Kornak U
Efficient generation of osteoclasts from human induced pluripotent stem cells and functional investigations of lethal CLCN7-related osteopetrosis
Rössler U et al. Efficient generation of osteoclasts from human induced pluripotent stem cells and functional investigations of lethal CLCN7-related osteopetrosis. . 2021-08-00. Pubmed ID: 33905594; DOI: 10.1002/jbmr.4322 BIHi002-A 2021-08-00 2021-08-00 PubMed: 33905594 DOI: 10.1002/jbmr.4322Associated cell lines:
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Machowska M, Bearzi C, Piekarowicz K, Łaczmańska I, Rzepecki R
Generation of one control and four iPSCs clones from patients with Emery-Dreifuss muscular dystrophy type 1
Machowska M et al. Generation of one control and four iPSCs clones from patients with Emery-Dreifuss muscular dystrophy type 1. . 2021-08-00. Pubmed ID: 34419748; DOI: 10.1016/j.scr.2021.102487 UWRBTi001-AUWRBTi003-BUWRBTi003-CUWRBTi004-AUWRBTi004-B 2021-08-00 2021-08-00 PubMed: 34419748 DOI: 10.1016/j.scr.2021.102487Associated cell lines:
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Choi NY, Lee Y, Park YS, Ko K, Park B, Koh YG
Establishment of an integration-free human induced pluripotent stem cell line (TJCi001-A) from normal bone marrow-derived mesenchymal stem cells
Choi NY et al. Establishment of an integration-free human induced pluripotent stem cell line (TJCi001-A) from normal bone marrow-derived mesenchymal stem cells. . 2021-08-00. Pubmed ID: 34371346; DOI: 10.1016/j.scr.2021.102484 TJCi001-A 2021-08-00 2021-08-00 PubMed: 34371346 DOI: 10.1016/j.scr.2021.102484Associated cell lines:
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Park HJ, Jeon J, Choi J, Kim JY, Kim HS, Huh JY, Goldman SA, Song J
Human iPSC-derived neural precursor cells differentiate into multiple cell types to delay disease progression following transplantation into YAC128 Huntington's disease mouse model
Park HJ et al. Human iPSC-derived neural precursor cells differentiate into multiple cell types to delay disease progression following transplantation into YAC128 Huntington's disease mouse model. . 2021-08-00. Pubmed ID: 34152047; DOI: 10.1111/cpr.13082; PMC: PMC8349664 CHAi001-A 2021-08-00 2021-08-00 PubMed: 34152047 DOI: 10.1111/cpr.13082Associated cell lines:
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Schoger E, Zimmermann WH, Cyganek L, Zelarayán LC
Establishment of two homozygous CRISPR interference (CRISPRi) knock-in human induced pluripotent stem cell (hiPSC) lines for titratable endogenous gene repression
Schoger E et al. Establishment of two homozygous CRISPR interference (CRISPRi) knock-in human induced pluripotent stem cell (hiPSC) lines for titratable endogenous gene repression. . 2021-08-00. Pubmed ID: 34343828; DOI: 10.1016/j.scr.2021.102473 RUCDRi002-A-16RUCDRi002-A-17 2021-08-00 2021-08-00 PubMed: 34343828 DOI: 10.1016/j.scr.2021.102473Associated cell lines:
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Nourbakhsh A, Gosstola NC, Fernandez-Valle C, Dykxhoorn DM, Liu XZ
Characterization of UMi031-A-2 inducible pluripotent stem cell line with a neurofibromatosis type 2-associated mutation
Nourbakhsh A et al. Characterization of UMi031-A-2 inducible pluripotent stem cell line with a neurofibromatosis type 2-associated mutation. . 2021-08-00. Pubmed ID: 34352618; DOI: 10.1016/j.scr.2021.102474 HVRDi004-BHVRDi004-B-2 2021-08-00 2021-08-00 PubMed: 34352618 DOI: 10.1016/j.scr.2021.102474Associated cell lines:
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Ramme AP, Faust D, Koenig L, Nguyen N, Marx U
Supporting dataset of two integration-free induced pluripotent stem cell lines from related human donors
Ramme AP et al. Supporting dataset of two integration-free induced pluripotent stem cell lines from related human donors. . 2021-08-00. Pubmed ID: 34136596; DOI: 10.1016/j.dib.2021.107140; PMC: PMC8176322 TISSUi006-ATISSUi007-A 2021-08-00 2021-08-00 PubMed: 34136596 DOI: 10.1016/j.dib.2021.107140Associated cell lines:
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Chaudhry A, Anthanasiou-Fragkouli A, Houlden H
DRPLA: understanding the natural history and developing biomarkers to accelerate therapeutic trials in a globally rare repeat expansion disorder
Chaudhry A et al. DRPLA: understanding the natural history and developing biomarkers to accelerate therapeutic trials in a globally rare repeat expansion disorder. . 2021-08-00. Pubmed ID: 33106889; DOI: 10.1007/s00415-020-10218-6; PMC: PMC8289787 CSSi008-A 2021-08-00 2021-08-00 PubMed: 33106889 DOI: 10.1007/s00415-020-10218-6Associated cell lines:
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Boehnke J, Atakhanov S, Toledo MAS, Schüler HM, Sontag S, Chatain N, Koschmieder S, Brümmendorf TH, Kramann R, Zenke M
CRISPR/Cas9 mediated CXCL4 knockout in human iPS cells of polycythemia vera patient with JAK2 V617F mutation
Boehnke J et al. CRISPR/Cas9 mediated CXCL4 knockout in human iPS cells of polycythemia vera patient with JAK2 V617F mutation. . 2021-08-00. Pubmed ID: 34391098; DOI: 10.1016/j.scr.2021.102490 UKAi002-AUKAi002-BUKAi002-A-1UKAi002-B-1 2021-08-00 2021-08-00 PubMed: 34391098 DOI: 10.1016/j.scr.2021.102490Associated cell lines:
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Usman A, Haase A, Merkert S, Göhring G, Hansmann G, Gall H, Schermuly R, Martin U, Olmer R
Generation of pulmonary arterial hypertension patient-specific induced pluripotent stem cell lines from three unrelated patients with a heterozygous missense mutation in exon 12, a heterozygous in-frame deletion in exon 3 and a missense mutation in exon 11 of the BMPR2 gene
Usman A et al. Generation of pulmonary arterial hypertension patient-specific induced pluripotent stem cell lines from three unrelated patients with a heterozygous missense mutation in exon 12, a heterozygous in-frame deletion in exon 3 and a missense mutation in exon 11 of the BMPR2 gene. . 2021-08-00. Pubmed ID: 34388490; DOI: 10.1016/j.scr.2021.102488 MHHi022-AMHHi023-AMHHi024-A 2021-08-00 2021-08-00 PubMed: 34388490 DOI: 10.1016/j.scr.2021.102488 -
Mazza MC, Beilina A, Roosen DA, Hauser D, Cookson MR
Generation of iPSC line from a Parkinson patient with PARK7 mutation and CRISPR-edited Gibco human episomal iPSC line to mimic PARK7 mutation
Mazza MC et al. Generation of iPSC line from a Parkinson patient with PARK7 mutation and CRISPR-edited Gibco human episomal iPSC line to mimic PARK7 mutation. . 2021-08-00. Pubmed ID: 34419745; DOI: 10.1016/j.scr.2021.102506; PMC: PMC8451958 TMOi001-ANIHTVBi015-ATMOi001-A-3 2021-08-00 2021-08-00 PubMed: 34419745 DOI: 10.1016/j.scr.2021.102506Associated cell lines:
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Cao X, Jahng JWS, Lee C, Zha Y, Wheeler MT, Sallam K, Wu JC
Generation of three induced pluripotent stem cell lines from hypertrophic cardiomyopathy patients carrying MYH7 mutations
Cao X et al. Generation of three induced pluripotent stem cell lines from hypertrophic cardiomyopathy patients carrying MYH7 mutations. . 2021-08-00. Pubmed ID: 34352619; DOI: 10.1016/j.scr.2021.102455; PMC: PMC10339835 SCVIi006-ASCVIi007-ASCVIi008-A 2021-08-00 2021-08-00 PubMed: 34352619 DOI: 10.1016/j.scr.2021.102455Associated cell lines:
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Xiang Bitao, Zhu Shichao, Li Jun, Lai Hao, Wang Chunsheng, Zhu Kai
Current Pharmacological Management of Aortic Aneurysm
Xiang Bitao et al. Current Pharmacological Management of Aortic Aneurysm. . 2021-08-00. DOI: 10.1097/fjc.0000000000001054 ISMMSi002-B 2021-08-00 2021-08-00 DOI: 10.1097/fjc.0000000000001054Associated cell lines:
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Yada Y, Suga M, Shibukawa R, Sagara Y, Okanishi Y, Enami T, Tsukita K, Kondo T, Imamura K, Sugihara G, Murai T, Inoue H
Establishment of induced pluripotent stem cells from schizophrenia discordant fraternal twins
Yada Y et al. Establishment of induced pluripotent stem cells from schizophrenia discordant fraternal twins. . 2021-08-00. Pubmed ID: 34419750; DOI: 10.1016/j.scr.2021.102504 BRCi003-ABRCi015-A 2021-08-00 2021-08-00 PubMed: 34419750 DOI: 10.1016/j.scr.2021.102504 -
Martello F, Lattante S, Doronzio PN, Conte A, Bisogni G, Orteschi D, Pirozzi F, Sabatelli M, Zollino M, Marangi G
Generation of an induced pluripotent stem cell line (UCSCi001-A) from a patient with early-onset amyotrophic lateral sclerosis carrying a FUS variant
Martello F et al. Generation of an induced pluripotent stem cell line (UCSCi001-A) from a patient with early-onset amyotrophic lateral sclerosis carrying a FUS variant. . 2021-08-00. Pubmed ID: 34303285; DOI: 10.1016/j.scr.2021.102461 UCSCi001-A 2021-08-00 2021-08-00 PubMed: 34303285 DOI: 10.1016/j.scr.2021.102461Associated cell lines:
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Ma S, Xu Q, Bai R, Dong T, Peng Z, Liu X
Generation of a TPM1 homozygous knockout embryonic stem cell line by CRISPR/Cas9 editing
Ma S et al. Generation of a TPM1 homozygous knockout embryonic stem cell line by CRISPR/Cas9 editing. . 2021-08-00. Pubmed ID: 34352617; DOI: 10.1016/j.scr.2021.102470 WAe009-AWAe009-A-36WAe009-A-61WAe009-A-1E 2021-08-00 2021-08-00 PubMed: 34352617 DOI: 10.1016/j.scr.2021.102470Associated cell lines:
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Aarts CEM, Varga E, Webbers S, Geissler J, von Lindern M, Kuijpers TW, van den Akker E
Generation and characterization of a human iPSC line SANi007-A from a patient with a heterozygous dominant mutation in ELANE
Aarts CEM et al. Generation and characterization of a human iPSC line SANi007-A from a patient with a heterozygous dominant mutation in ELANE. . 2021-08-00. Pubmed ID: 34229202; DOI: 10.1016/j.scr.2021.102440 SANi007-A 2021-08-00 2021-08-00 PubMed: 34229202 DOI: 10.1016/j.scr.2021.102440Associated cell lines:
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Zhang W, Di W, Zhao J, Zhang B, Wang Y
Generation of a SIAISi004-A hiPSC line from PBMCs of a 74 year-old Alzheimer's disease woman by non-integrating sendai virus mediated reprogramming
Zhang W et al. Generation of a SIAISi004-A hiPSC line from PBMCs of a 74 year-old Alzheimer's disease woman by non-integrating sendai virus mediated reprogramming. . 2021-08-00. Pubmed ID: 34450529; DOI: 10.1016/j.scr.2021.102501 SIAISi004-A 2021-08-00 2021-08-00 PubMed: 34450529 DOI: 10.1016/j.scr.2021.102501Associated cell lines:
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Meraviglia V, Cattelan G, De Bortoli M, Motta BM, Volpato C, Frommelt LS, Rauhe W, Di Segni M, Silipigni R, Pramstaller PP, Rossini A
Generation and characterization of three human induced pluripotent stem cell lines (EURACi007-A, EURACi008-A, EURACi009-A) from three different individuals of the same family with arrhythmogenic cardiomyopathy (ACM) carrying the plakophillin2 p.N346Lfs*12 mutation
Meraviglia V et al. Generation and characterization of three human induced pluripotent stem cell lines (EURACi007-A, EURACi008-A, EURACi009-A) from three different individuals of the same family with arrhythmogenic cardiomyopathy (ACM) carrying the plakophillin2 p.N346Lfs*12 mutation. . 2021-08-00. Pubmed ID: 34298432; DOI: 10.1016/j.scr.2021.102466 EURACi007-AEURACi008-AEURACi009-A 2021-08-00 2021-08-00 PubMed: 34298432 DOI: 10.1016/j.scr.2021.102466Associated cell lines:
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Xia Q, Yang X, Shi J, Liu Z, Peng Y, Wang W, Li B, Zhao Y, Xiao J, Huang L, Wang D, Gao X
The Protective A673T Mutation of Amyloid Precursor Protein (APP) in Alzheimer's Disease
Xia Q et al. The Protective A673T Mutation of Amyloid Precursor Protein (APP) in Alzheimer's Disease. . 2021-08-00. Pubmed ID: 33914267; DOI: 10.1007/s12035-021-02385-y UEFi003-A 2021-08-00 2021-08-00 PubMed: 33914267 DOI: 10.1007/s12035-021-02385-yAssociated cell lines:
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Zhai L, Shen H, Sheng Y, Guan Q
ADMSC Exo-MicroRNA-22 improve neurological function and neuroinflammation in mice with Alzheimer's disease
Zhai L et al. ADMSC Exo-MicroRNA-22 improve neurological function and neuroinflammation in mice with Alzheimer's disease. . 2021-08-00. Pubmed ID: 34250722; DOI: 10.1111/jcmm.16787; PMC: PMC8335682 IRMBi001-A 2021-08-00 2021-08-00 PubMed: 34250722 DOI: 10.1111/jcmm.16787Associated cell lines:
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Guo L, Zhao Z, Zhao S, Kong F, Yuan M
Generation of an iPSC line (HRMSDUi001-A) from an azoospermic patient with 45,XY,der(13;14)(q10;q10) karyotype
Guo L et al. Generation of an iPSC line (HRMSDUi001-A) from an azoospermic patient with 45,XY,der(13;14)(q10;q10) karyotype. . 2021-08-00. Pubmed ID: 34284274; DOI: 10.1016/j.scr.2021.102453 HRMSDUi001-A 2021-08-00 2021-08-00 PubMed: 34284274 DOI: 10.1016/j.scr.2021.102453Associated cell lines:
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Tian L, Wu F, Bai R, Ma S, Zheng H, Liu WJ, Wang Y
Generation of a COL4A5 heterozygous mutation human embryonic stem cell line (WAe009-A-58) using an episomal vector-based CRISPR/Cas9 system
Tian L et al. Generation of a COL4A5 heterozygous mutation human embryonic stem cell line (WAe009-A-58) using an episomal vector-based CRISPR/Cas9 system. . 2021-08-00. Pubmed ID: 34419749; DOI: 10.1016/j.scr.2021.102481 WAe009-AWAe009-A-58 2021-08-00 2021-08-00 PubMed: 34419749 DOI: 10.1016/j.scr.2021.102481Associated cell lines:
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Warnecke N, Ulmer BM, Laufer SD, Shibamiya A, Krämer E, Neuber C, Hanke S, Behrens C, Loos M, Münch J, Kühnisch J, Klaassen S, Eschenhagen T, Patten-Hamel M, Carrier L, Mearini G
Generation of bi-allelic MYBPC3 truncating mutant and isogenic control from an iPSC line of a patient with hypertrophic cardiomyopathy
Warnecke N et al. Generation of bi-allelic MYBPC3 truncating mutant and isogenic control from an iPSC line of a patient with hypertrophic cardiomyopathy. . 2021-08-00. Pubmed ID: 34375846; DOI: 10.1016/j.scr.2021.102489 UKEi070-AUKEi070-A-1UKEi070-A-2 2021-08-00 2021-08-00 PubMed: 34375846 DOI: 10.1016/j.scr.2021.102489Associated cell lines:
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Martins S, Hacheney I, Teichweyde N, Hildebrandt B, Krutmann J, Rossi A
Generation of an induced pluripotent stem cell line (IUFi001) from a Cockayne syndrome patient carrying a mutation in the ERCC6 gene
Martins S et al. Generation of an induced pluripotent stem cell line (IUFi001) from a Cockayne syndrome patient carrying a mutation in the ERCC6 gene. . 2021-08-00. Pubmed ID: 34271225; DOI: 10.1016/j.scr.2021.102456 IUFi001-A 2021-08-00 2021-08-00 PubMed: 34271225 DOI: 10.1016/j.scr.2021.102456Associated cell lines:
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Zhang Z, Si N, Pan B, Jiang H
Generation of a human induced pluripotent stem cell line (PSHi002-A) from a Treacher-Collins syndrome patient carrying a TCOF1 gene mutation (c.1966_1969dup)
Zhang Z et al. Generation of a human induced pluripotent stem cell line (PSHi002-A) from a Treacher-Collins syndrome patient carrying a TCOF1 gene mutation (c.1966_1969dup). . 2021-08-00. Pubmed ID: 34247110; DOI: 10.1016/j.scr.2021.102437 PSHi002-A 2021-08-00 2021-08-00 PubMed: 34247110 DOI: 10.1016/j.scr.2021.102437Associated cell lines:
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Shahryari A, Moya N, Siehler J, Wang X, Burtscher I, Lickert H
Increasing Gene Editing Efficiency for CRISPR-Cas9 by Small RNAs in Pluripotent Stem Cells
Shahryari A et al. Increasing Gene Editing Efficiency for CRISPR-Cas9 by Small RNAs in Pluripotent Stem Cells. . 2021-08-00. Pubmed ID: 34406042; DOI: 10.1089/crispr.2021.0014 HMGUi001-AHMGUi002-AHMGUi001-A-5 2021-08-00 2021-08-00 PubMed: 34406042 DOI: 10.1089/crispr.2021.0014Associated cell lines:
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Ropret S, Jeriha J, Sorčan T, Rogar M, Zemljič Jokhadar Š, McGrath JA, Ilic D, Liovic M
Induced pluripotent stem cell (iPSC) line MLi-004A derived from a patient with recessive dystrophic epidermolysis bullosa (RDEB)
Ropret S et al. Induced pluripotent stem cell (iPSC) line MLi-004A derived from a patient with recessive dystrophic epidermolysis bullosa (RDEB). . 2021-08-00. Pubmed ID: 34284275; DOI: 10.1016/j.scr.2021.102463 KCLi003-AMLi004-A 2021-08-00 2021-08-00 PubMed: 34284275 DOI: 10.1016/j.scr.2021.102463 -
Dor L, Rabinski T, Zlotnik D, Shilian M, Weil M, Vatine GD
Induced pluripotent stem cell (iPSC) lines from two individuals carrying a homozygous (BGUi007-A) and a heterozygous (BGUi006-A) mutation in ELP1 for in vitro modeling of familial dysautonomia
Dor L et al. Induced pluripotent stem cell (iPSC) lines from two individuals carrying a homozygous (BGUi007-A) and a heterozygous (BGUi006-A) mutation in ELP1 for in vitro modeling of familial dysautonomia. . 2021-08-00. Pubmed ID: 34419746; DOI: 10.1016/j.scr.2021.102495 BGUi004-ABGUi005-ABGUi006-ABGUi007-A 2021-08-00 2021-08-00 PubMed: 34419746 DOI: 10.1016/j.scr.2021.102495 -
Aarts CEM, Varga E, Webbers S, Geissler J, von Lindern M, Kuijpers TW, van den Akker E
Generation and characterization of a human iPSC line SANi008-A from a Chédiak-Higashi Syndrome patient
Aarts CEM et al. Generation and characterization of a human iPSC line SANi008-A from a Chédiak-Higashi Syndrome patient. . 2021-08-00. Pubmed ID: 34224985; DOI: 10.1016/j.scr.2021.102442 SANi008-A 2021-08-00 2021-08-00 PubMed: 34224985 DOI: 10.1016/j.scr.2021.102442Associated cell lines:
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Pan Z, Wang H, Wang H, Liu Y, Liang P
Generation of an induced pluripotent stem cell line from a patient carrying FBN1/c.6734 G > A mutation
Pan Z et al. Generation of an induced pluripotent stem cell line from a patient carrying FBN1/c.6734 G > A mutation. . 2021-08-00. Pubmed ID: 34298435; DOI: 10.1016/j.scr.2021.102459 ZJUi005-A 2021-08-00 2021-08-00 PubMed: 34298435 DOI: 10.1016/j.scr.2021.102459Associated cell lines:
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Aarts CEM, Varga E, Webbers S, Geissler J, von Lindern M, Kuijpers TW, van den Akker E
Generation and characterization of a human iPSC line SANi006-A from a Gray Platelet Syndrome patient
Aarts CEM et al. Generation and characterization of a human iPSC line SANi006-A from a Gray Platelet Syndrome patient. . 2021-08-00. Pubmed ID: 34237592; DOI: 10.1016/j.scr.2021.102443 SANi006-A 2021-08-00 2021-08-00 PubMed: 34237592 DOI: 10.1016/j.scr.2021.102443Associated cell lines:
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Chen D, Song B, Cheng Y, Zhu L, Lu D, Liu N, Yang Y, Sun X
Generation of a homozygous ZBTB7A knockout human induced pluripotent stem line by CRISPR/Cas9 editing
Chen D et al. Generation of a homozygous ZBTB7A knockout human induced pluripotent stem line by CRISPR/Cas9 editing. . 2021-08-00. Pubmed ID: 34403853; DOI: 10.1016/j.scr.2021.102494 GZHMCi007-A 2021-08-00 2021-08-00 PubMed: 34403853 DOI: 10.1016/j.scr.2021.102494Associated cell lines:
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Kim JH, Kang KW, Lee BH, Park Y, Kim BS
Generation of induced pluripotent stem cell line KUMi002-A with normal karyotype from a patient with Philadelphia chromosome-positive chronic myeloid leukemia
Kim JH et al. Generation of induced pluripotent stem cell line KUMi002-A with normal karyotype from a patient with Philadelphia chromosome-positive chronic myeloid leukemia. . 2021-08-00. Pubmed ID: 34303284; DOI: 10.1016/j.scr.2021.102465 KUMCi001-AKUMCi002-AKUMi002-A 2021-08-00 2021-08-00 PubMed: 34303284 DOI: 10.1016/j.scr.2021.102465Associated cell lines:
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Sun H, Wang Z, Zhang Q, Liu Y, Yang J, Liu H, Shi C, Wang Y, Xu Y
Generation of induced pluripotent stem cell line (ZZUi027-A) derived from skin fibroblasts from a Parkinson's disease patient with RAB39B gene mutation
Sun H et al. Generation of induced pluripotent stem cell line (ZZUi027-A) derived from skin fibroblasts from a Parkinson's disease patient with RAB39B gene mutation. . 2021-08-00. Pubmed ID: 34247111; DOI: 10.1016/j.scr.2021.102454 ZZUi005-AZZUi027-AZZUi037-A 2021-08-00 2021-08-00 PubMed: 34247111 DOI: 10.1016/j.scr.2021.102454 -
Zhu Y, Zhang L, Wang G, Zhao J, Hou X, Wu H, Xu Y, Mao J, Liu Z, Zhang J
Generation of an induced pluripotent stem cell line (ZJUi007-A) from a 11-year-old patient of Fabry disease
Zhu Y et al. Generation of an induced pluripotent stem cell line (ZJUi007-A) from a 11-year-old patient of Fabry disease. . 2021-08-00. Pubmed ID: 34365103; DOI: 10.1016/j.scr.2021.102475 ZJUi007-A 2021-08-00 2021-08-00 PubMed: 34365103 DOI: 10.1016/j.scr.2021.102475Associated cell lines:
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Krisch L, Brachtl G, Hochmann S, Andrade AC, Oeller M, Ebner-Peking P, Schallmoser K, Strunk D
Improving Human Induced Pluripotent Stem Cell-Derived Megakaryocyte Differentiation and Platelet Production
Krisch L et al. Improving Human Induced Pluripotent Stem Cell-Derived Megakaryocyte Differentiation and Platelet Production. . 2021-07-30. Pubmed ID: 34360992; DOI: 10.3390/ijms22158224; PMC: PMC8348107 BIHi001-A 2021-07-30 2021-07-30 PubMed: 34360992 DOI: 10.3390/ijms22158224Associated cell lines:
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Lodola F, De Giusti VC, Maniezzi C, Martone D, Stadiotti I, Sommariva E, Maione AS
Modeling Cardiomyopathies in a Dish: State-of-the-Art and Novel Perspectives on hiPSC-Derived Cardiomyocytes Maturation
Lodola F et al. Modeling Cardiomyopathies in a Dish: State-of-the-Art and Novel Perspectives on hiPSC-Derived Cardiomyocytes Maturation. . 2021-07-30. Pubmed ID: 34439963; DOI: 10.3390/biology10080730; PMC: PMC8389603 LUMCi027-A 2021-07-30 2021-07-30 PubMed: 34439963 DOI: 10.3390/biology10080730Associated cell lines:
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Mazurek S, Oleksiewicz U, Czerwińska P, Wróblewska J, Klimczak M, Wiznerowicz M
Disruption of RING and PHD Domains of TRIM28 Evokes Differentiation in Human iPSCs
Mazurek S et al. Disruption of RING and PHD Domains of TRIM28 Evokes Differentiation in Human iPSCs. . 2021-07-29. Pubmed ID: 34440702; DOI: 10.3390/cells10081933; PMC: PMC8394524 NYSCFe003-A 2021-07-29 2021-07-29 PubMed: 34440702 DOI: 10.3390/cells10081933Associated cell lines:
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Martinat C, Cormier A, Tobaly-Tapiero J, Palmic N, Casartelli N, Mahboubi B, Coggins SA, Buchrieser J, Persaud M, Diaz-Griffero F, Espert L, Bossis G, Lesage P, Schwartz O, Kim B, Margottin-Goguet F, Saïb A, Zamborlini A
SUMOylation of SAMHD1 at Lysine 595 is required for HIV-1 restriction in non-cycling cells
Martinat C et al. SUMOylation of SAMHD1 at Lysine 595 is required for HIV-1 restriction in non-cycling cells. . 2021-07-28. Pubmed ID: 34321470; DOI: 10.1038/s41467-021-24802-5; PMC: PMC8319325 STBCi044-A 2021-07-28 2021-07-28 PubMed: 34321470 DOI: 10.1038/s41467-021-24802-5Associated cell lines:
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Wong CY
Current advances of stem cell-based therapy for kidney diseases
Wong CY. Current advances of stem cell-based therapy for kidney diseases. . 2021-07-26. Pubmed ID: 34367484; DOI: 10.4252/wjsc.v13.i7.914; PMC: PMC8316868 NCCSi002-A 2021-07-26 2021-07-26 PubMed: 34367484 DOI: 10.4252/wjsc.v13.i7.914Associated cell lines:
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Jarrige M, Polvèche H, Carteron A, Janczarski S, Peschanski M, Auboeuf D, Martinat C
SISTEMA: A large and standardized collection of transcriptome data sets for human pluripotent stem cell research
Jarrige M et al. SISTEMA: A large and standardized collection of transcriptome data sets for human pluripotent stem cell research. . 2021-07-23. Pubmed ID: 34278269; DOI: 10.1016/j.isci.2021.102767; PMC: PMC8271161 CEBe033-ARCe013-ARCe021-A 2021-07-23 2021-07-23 PubMed: 34278269 DOI: 10.1016/j.isci.2021.102767 -
Rafieerad A, Amiri A, Sequiera GL, Yan W, Chen Y, Polycarpou AA, Dhingra S
Development of Fluorine-Free Tantalum Carbide MXene Hybrid Structure as a Biocompatible Material for Supercapacitor Electrodes
Rafieerad A et al. Development of Fluorine-Free Tantalum Carbide MXene Hybrid Structure as a Biocompatible Material for Supercapacitor Electrodes. . 2021-07-23. Pubmed ID: 35264918; DOI: 10.1002/adfm.202100015; PMC: PMC8889894 UOMi002-AUOMi005-A 2021-07-23 2021-07-23 PubMed: 35264918 DOI: 10.1002/adfm.202100015 -
McKnight CL, Low YC, Elliott DA, Thorburn DR, Frazier AE
Modelling Mitochondrial Disease in Human Pluripotent Stem Cells: What Have We Learned?
McKnight CL et al. Modelling Mitochondrial Disease in Human Pluripotent Stem Cells: What Have We Learned?. . 2021-07-20. Pubmed ID: 34299348; DOI: 10.3390/ijms22147730; PMC: PMC8306397 WAe009-AIISHDOi003-AIBMSi004-AZJUCHi002-AUAMi004-AFINCBi001-AIISHDOi006-ASHCDNi001-ALUMCi024-ALUMCi025-ALUMCi026-AUOMi001-AJUCTCi012-AWMUi002-AUOMi002-ALIBUCi001-ALIBUCi002-AXACHi010-AJMUi001-AJMUi001-A-1FINCBi002-AFINCBi003-AWAe009-A-47BIOi002-ACPGHi003-A 2021-07-20 2021-07-20 PubMed: 34299348 DOI: 10.3390/ijms22147730Associated cell lines:
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Sattler K, El-Battrawy I, Cyganek L, Lang S, Lan H, Li X, Zhao Z, Utikal J, Wieland T, Borggrefe M, Zhou X, Akin I
TRPV1 activation and internalization is part of the LPS-induced inflammation in human iPSC-derived cardiomyocytes
Sattler K et al. TRPV1 activation and internalization is part of the LPS-induced inflammation in human iPSC-derived cardiomyocytes. . 2021-07-19. Pubmed ID: 34282193; DOI: 10.1038/s41598-021-93958-3; PMC: PMC8289830 UMGi124-AUMGi014-BUMGi130-A 2021-07-19 2021-07-19 PubMed: 34282193 DOI: 10.1038/s41598-021-93958-3 -
Chen CX, Abdian N, Maussion G, Thomas RA, Demirova I, Cai E, Tabatabaei M, Beitel LK, Karamchandani J, Fon EA, Durcan TM
A Multistep Workflow to Evaluate Newly Generated iPSCs and Their Ability to Generate Different Cell Types
Chen CX et al. A Multistep Workflow to Evaluate Newly Generated iPSCs and Their Ability to Generate Different Cell Types. . 2021-07-19. Pubmed ID: 34287353; DOI: 10.3390/mps4030050; PMC: PMC8293472 KUIFMSi004-CCBIGi001-A 2021-07-19 2021-07-19 PubMed: 34287353 DOI: 10.3390/mps4030050Associated cell lines:
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Polyak A, Bankstahl JP, Besecke KFW, Hozsa C, Triebert W, Pannem RR, Manstein F, Borcholte T, Furch M, Zweigerdt R, Gieseler RK, Bengel FM, Ross TL
Simplified (89)Zr-Labeling Protocol of Oxine (8-Hydroxyquinoline) Enabling Prolonged Tracking of Liposome-Based Nanomedicines and Cells
Polyak A et al. Simplified (89)Zr-Labeling Protocol of Oxine (8-Hydroxyquinoline) Enabling Prolonged Tracking of Liposome-Based Nanomedicines and Cells. . 2021-07-18. Pubmed ID: 34371788; DOI: 10.3390/pharmaceutics13071097; PMC: PMC8309181 MHHi001-AMHHi006-AMHHi001-A-5 2021-07-18 2021-07-18 PubMed: 34371788 DOI: 10.3390/pharmaceutics13071097Associated cell lines:
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Kopach O, Esteras N, Wray S, Abramov AY, Rusakov DA
Genetically engineered MAPT 10+16 mutation causes pathophysiological excitability of human iPSC-derived neurons related to 4R tau-induced dementia
Kopach O et al. Genetically engineered MAPT 10+16 mutation causes pathophysiological excitability of human iPSC-derived neurons related to 4R tau-induced dementia. . 2021-07-17. Pubmed ID: 34274950; DOI: 10.1038/s41419-021-04007-w; PMC: PMC8286258 SIGi001-ASIGi001-A-1SIGi001-A-13 2021-07-17 2021-07-17 PubMed: 34274950 DOI: 10.1038/s41419-021-04007-wAssociated cell lines:
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Fortschegger K, Husa AM, Schinnerl D, Nebral K, Strehl S
Expression of RUNX1-JAK2 in Human Induced Pluripotent Stem Cell-Derived Hematopoietic Cells Activates the JAK-STAT and MYC Pathways
Fortschegger K et al. Expression of RUNX1-JAK2 in Human Induced Pluripotent Stem Cell-Derived Hematopoietic Cells Activates the JAK-STAT and MYC Pathways. . 2021-07-15. Pubmed ID: 34299194; DOI: 10.3390/ijms22147576; PMC: PMC8304339 TMOi001-A 2021-07-15 2021-07-15 PubMed: 34299194 DOI: 10.3390/ijms22147576Associated cell lines:
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Pathan N, Shende P
Tailoring of P-glycoprotein for effective transportation of actives across blood-brain-barrier
Pathan N et al. Tailoring of P-glycoprotein for effective transportation of actives across blood-brain-barrier. . 2021-07-10. Pubmed ID: 34087246; DOI: 10.1016/j.jconrel.2021.05.046 BIONi010-C 2021-07-10 2021-07-10 PubMed: 34087246 DOI: 10.1016/j.jconrel.2021.05.046Associated cell lines:
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Zhu C, Wu J, Sun H, Briganti F, Meder B, Wei W, Steinmetz LM
Single-molecule, full-length transcript isoform sequencing reveals disease-associated RNA isoforms in cardiomyocytes
Zhu C et al. Single-molecule, full-length transcript isoform sequencing reveals disease-associated RNA isoforms in cardiomyocytes. . 2021-07-09. Pubmed ID: 34244519; DOI: 10.1038/s41467-021-24484-z; PMC: PMC8270901 UCSFi001-A-64UCSFi001-A-65 2021-07-09 2021-07-09 PubMed: 34244519 DOI: 10.1038/s41467-021-24484-zAssociated cell lines:
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Sone N, Konishi S, Igura K, Tamai K, Ikeo S, Korogi Y, Kanagaki S, Namba T, Yamamoto Y, Xu Y, Takeuchi K, Adachi Y, Chen-Yoshikawa TF, Date H, Hagiwara M, Tsukita S, Hirai T, Torisawa YS, Gotoh S
Multicellular modeling of ciliopathy by combining iPS cells and microfluidic airway-on-a-chip technology
Sone N et al. Multicellular modeling of ciliopathy by combining iPS cells and microfluidic airway-on-a-chip technology. . 2021-07-07. Pubmed ID: 34233948; DOI: 10.1126/scitranslmed.abb1298 UHOMi001-A 2021-07-07 2021-07-07 PubMed: 34233948 DOI: 10.1126/scitranslmed.abb1298Associated cell lines:
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Varró A, Tomek J, Nagy N, Virág L, Passini E, Rodriguez B, Baczkó I
Cardiac transmembrane ion channels and action potentials: cellular physiology and arrhythmogenic behavior
Varró A et al. Cardiac transmembrane ion channels and action potentials: cellular physiology and arrhythmogenic behavior. . 2021-07-01. Pubmed ID: 33118864; DOI: 10.1152/physrev.00024.2019 PSMi006-A 2021-07-01 2021-07-01 PubMed: 33118864 DOI: 10.1152/physrev.00024.2019Associated cell lines:
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Polyak A, Bankstahl J, Besecke K, Hozsa C, Triebert W, Pannem R, Manstein F, Borcholte T, Furch M, Zweigerdt R, Gieseler R, Bengel F, Ross T.
Simplified 89Zr-Labeling Protocol of Oxine (8-Hydroxyquinoline) Enabling Prolonged Tracking of Liposome-Based Nanomedicines and Cells
Polyak A et al. Simplified 89Zr-Labeling Protocol of Oxine (8-Hydroxyquinoline) Enabling Prolonged Tracking of Liposome-Based Nanomedicines and Cells. . 2021-07-01. MHHi001-AMHHi006-AMHHi001-A-5 2021-07-01 2021-07-01Associated cell lines:
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Borsoi J, Farinha-Arcieri LE, Morato-Marques M, Delgado Sarafian R, Pinheiro M, Veiga Pereira L
Generation of genetically modified human induced pluripotent stem cell lines harboring haploin sufficient or dominant negative variants in the FBN1 gene
Borsoi J et al. Generation of genetically modified human induced pluripotent stem cell lines harboring haploin sufficient or dominant negative variants in the FBN1 gene. . 2021-07-00. Pubmed ID: 34174776; DOI: 10.1016/j.scr.2021.102434 LANCEi020-ALANCEi020-A-1LANCEi020-A-2LANCEi020-A-3LANCEi020-A-4LANCEi020-A-5LANCEi020-A-6LANCEi020-A-7LANCEi020-A-8LANCEi020-A-9LANCEi020-A-10 2021-07-00 2021-07-00 PubMed: 34174776 DOI: 10.1016/j.scr.2021.102434 -
Chiu YT, Tsai MH, Chan DZ, Ko HW, Lu HE, Huang CF, Lin YJ, Chang SL, Lo LW, Huang CY, Hu YF, Hsieh PCH, Chen SA
Generation of IBMS-iPSC-015, -016, -017 human induced pluripotent stem cells (IBMSi013-A, IBMSi014-A, and IBMSi015-A) derived from patients with atrial fibrillation
Chiu YT et al. Generation of IBMS-iPSC-015, -016, -017 human induced pluripotent stem cells (IBMSi013-A, IBMSi014-A, and IBMSi015-A) derived from patients with atrial fibrillation. . 2021-07-00. Pubmed ID: 34119955; DOI: 10.1016/j.scr.2021.102419 IBMSi013-AIBMSi014-AIBMSi015-A 2021-07-00 2021-07-00 PubMed: 34119955 DOI: 10.1016/j.scr.2021.102419Associated cell lines:
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Fischer I, Küchler J, Schaar C, Fisch T, Cernoch J, Fischer K, Fernández Vallone V, Kühnen P, Stachelscheid H
Generation of human induced pluripotent stem cell lines from 2 patients with MIRAGE syndrome
Fischer I et al. Generation of human induced pluripotent stem cell lines from 2 patients with MIRAGE syndrome. . 2021-07-00. Pubmed ID: 34119956; DOI: 10.1016/j.scr.2021.102417 CUBi001-ACUBi002-B 2021-07-00 2021-07-00 PubMed: 34119956 DOI: 10.1016/j.scr.2021.102417 -
Beltran AA, Molina SG, Marquez A, Munoz LJ, Olivares JF, Beltran AS
Generation of an induced pluripotent stem cell line (UNCCi002-A) from a healthy donor using a non-integration system to study Cerebral Cavernous Malformation (CCM)
Beltran AA et al. Generation of an induced pluripotent stem cell line (UNCCi002-A) from a healthy donor using a non-integration system to study Cerebral Cavernous Malformation (CCM). . 2021-07-00. Pubmed ID: 34130156; DOI: 10.1016/j.scr.2021.102421 UNCi002-A 2021-07-00 2021-07-00 PubMed: 34130156 DOI: 10.1016/j.scr.2021.102421Associated cell lines:
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Shih PY, Kreir M, Kumar D, Seibt F, Pestana F, Schmid B, Holst B, Clausen C, Steeg R, Fischer B, Pita-Almenar J, Ebneth A, Cabrera-Socorro A
Development of a fully human assay combining NGN2-inducible neurons co-cultured with iPSC-derived astrocytes amenable for electrophysiological studies
Shih PY et al. Development of a fully human assay combining NGN2-inducible neurons co-cultured with iPSC-derived astrocytes amenable for electrophysiological studies. . 2021-07-00. Pubmed ID: 34229210; DOI: 10.1016/j.scr.2021.102386 BIONi010-CBIONi010-C-13BIONi010-C-15 2021-07-00 2021-07-00 PubMed: 34229210 DOI: 10.1016/j.scr.2021.102386Associated cell lines:
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Lavra L, Magi F, Ulivieri A, Morgante A, Paulis M, Sala L, Pedrazzini M, Polisca P, Rocchetti M, Calò L, Sciacchitano S, Salehi LB
Generation and characterization of the human induced pluripotent stem cell (hiPSC) line NCUFi001-A from a patient carrying KCNQ1 G314S mutation
Lavra L et al. Generation and characterization of the human induced pluripotent stem cell (hiPSC) line NCUFi001-A from a patient carrying KCNQ1 G314S mutation. . 2021-07-00. Pubmed ID: 34130155; DOI: 10.1016/j.scr.2021.102418 NCUFi001-A 2021-07-00 2021-07-00 PubMed: 34130155 DOI: 10.1016/j.scr.2021.102418Associated cell lines:
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Sarkar H, Méjécase C, Harding P, Eintracht J, Toualbi L, Cunha DL, Moosajee M
Generation of two human iPSC lines from patients with autosomal dominant retinitis pigmentosa (UCLi014-A) and autosomal recessive Leber congenital amaurosis (UCLi015-A), associated with RDH12 variants
Sarkar H et al. Generation of two human iPSC lines from patients with autosomal dominant retinitis pigmentosa (UCLi014-A) and autosomal recessive Leber congenital amaurosis (UCLi015-A), associated with RDH12 variants. . 2021-07-00. Pubmed ID: 34216980; DOI: 10.1016/j.scr.2021.102449; PMC: PMC8363920 UCLi014-AUCLi015-A 2021-07-00 2021-07-00 PubMed: 34216980 DOI: 10.1016/j.scr.2021.102449 -
Aarts CEM, Karampini E, Wüst T, Webbers S, Varga E, Geissler J, Voorberg J, von Lindern M, Bierings R, van den Akker E, Kuijpers TW
Generation and characterization of a control and patient-derived human iPSC line containing the Hermansky Pudlak type 2 (HPS2) associated heterozygous compound mutation in AP3B1
Aarts CEM et al. Generation and characterization of a control and patient-derived human iPSC line containing the Hermansky Pudlak type 2 (HPS2) associated heterozygous compound mutation in AP3B1. . 2021-07-00. Pubmed ID: 34182253; DOI: 10.1016/j.scr.2021.102444 SANi009-ASANi010-A 2021-07-00 2021-07-00 PubMed: 34182253 DOI: 10.1016/j.scr.2021.102444 -
Kelekçi S, Uğurlu-Çimen D, Demir AB, Özçimen B, Burak Yıldız A, Batuhan Karakuş M, Börklü Yücel E, Önder TT
Generation of transgene-free iPSC lines from three patients with Friedreich's ataxia (FRDA) carrying GAA triplet expansions in the first intron of FXN gene
Kelekçi S et al. Generation of transgene-free iPSC lines from three patients with Friedreich's ataxia (FRDA) carrying GAA triplet expansions in the first intron of FXN gene. . 2021-07-00. Pubmed ID: 34214898; DOI: 10.1016/j.scr.2021.102438 KUTTAMi001-AKUTTAMi002-AKUTTAMi003-A 2021-07-00 2021-07-00 PubMed: 34214898 DOI: 10.1016/j.scr.2021.102438Associated cell lines:
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Huang X, Roeder A, Li R, Beers J, Liu C, Zou J, Yu PB, Zheng W
Generation of an induced pluripotent stem cell line (TRNDi012-B) from Fibrodysplasia Ossificans Progressiva (FOP) patient carrying a heterozygous mutation c. 617G > A in the ACVR1 gene
Huang X et al. Generation of an induced pluripotent stem cell line (TRNDi012-B) from Fibrodysplasia Ossificans Progressiva (FOP) patient carrying a heterozygous mutation c. 617G > A in the ACVR1 gene. . 2021-07-00. Pubmed ID: 34139597; DOI: 10.1016/j.scr.2021.102424; PMC: PMC9428929 TRNDi012-B 2021-07-00 2021-07-00 PubMed: 34139597 DOI: 10.1016/j.scr.2021.102424Associated cell lines:
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Keller AL, Binner A, Breitmeyer R, Vogel S, Anderle N, Rothbauer U, Schenke-Layland K, Schmees C
Generation and characterization of the human induced pluripotent stem cell line NMIi010-A from peripheral blood mononuclear cells of a healthy 49-year old male individual
Keller AL et al. Generation and characterization of the human induced pluripotent stem cell line NMIi010-A from peripheral blood mononuclear cells of a healthy 49-year old male individual. . 2021-07-00. Pubmed ID: 34139596; DOI: 10.1016/j.scr.2021.102427 NMIi010-A 2021-07-00 2021-07-00 PubMed: 34139596 DOI: 10.1016/j.scr.2021.102427Associated cell lines:
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Yang J, Burgos Angulo M, Argenziano MA, Bertalovitz A, Najari Beidokhti M, McDonald TV
Generation of an iPSC cell line (USFi003-A) from a patient with dilated cardiomyopathy carrying a heterozygous mutation in LMNA (p.R541C)
Yang J et al. Generation of an iPSC cell line (USFi003-A) from a patient with dilated cardiomyopathy carrying a heterozygous mutation in LMNA (p.R541C). . 2021-07-00. Pubmed ID: 34029931; DOI: 10.1016/j.scr.2021.102396 USFi003-A 2021-07-00 2021-07-00 PubMed: 34029931 DOI: 10.1016/j.scr.2021.102396Associated cell lines:
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Elsayed AK, Al-Khawaga S, Hussain K, Abdelalim EM
An induced pluripotent stem cell line derived from a patient with neonatal diabetes and Fanconi-Bickel syndrome caused by a homozygous mutation in the SLC2A2 gene
Elsayed AK et al. An induced pluripotent stem cell line derived from a patient with neonatal diabetes and Fanconi-Bickel syndrome caused by a homozygous mutation in the SLC2A2 gene. . 2021-07-00. Pubmed ID: 34171785; DOI: 10.1016/j.scr.2021.102433 QBRIi007-AQBRIi012-A 2021-07-00 2021-07-00 PubMed: 34171785 DOI: 10.1016/j.scr.2021.102433Associated cell lines:
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Cernoch J, Fisch T, Fischer I, Fischer K, Iwanska A, Krüger N, Küchler J, Schaar C, Schommer S, Telugu N, Miller D, Fernández Vallone V, Kurtz A, Reinke P, Diecke S, Stachelscheid H
Generation of 20 human induced pluripotent stem cell lines from patients with focal segmental glomerulosclerosis (FSGS)
Cernoch J et al. Generation of 20 human induced pluripotent stem cell lines from patients with focal segmental glomerulosclerosis (FSGS). . 2021-07-00. Pubmed ID: 34062331; DOI: 10.1016/j.scr.2021.102406 BIHi002-ABIHi007-ABIHi008-ABIHi009-ABIHi010-ABIHi011-ABIHi012-ABIHi015-ABIHi016-ABIHi017-ABIHi018-ABIHi019-ABIHi024-ABIHi025-ABIHi028-BBIHi029-ABIHi030-CBIHi031-BBIHi032-ABIHi038-BBIHi006-D 2021-07-00 2021-07-00 PubMed: 34062331 DOI: 10.1016/j.scr.2021.102406 -
Ali E, Ferraro RM, Guglielmi A, Lanzi G, Masneri S, Piovani G, Mazzoldi EL, Pollara L, Valente EM, Accorsi P, Giordano L, Giliani SC
Establishment of three Joubert syndrome-derived induced pluripotent stem cell (iPSC) lines harbouring compound heterozygous mutations in CC2D2A gene
Ali E et al. Establishment of three Joubert syndrome-derived induced pluripotent stem cell (iPSC) lines harbouring compound heterozygous mutations in CC2D2A gene. . 2021-07-00. Pubmed ID: 34182252; DOI: 10.1016/j.scr.2021.102430 UNIBSi016-AUNIBSi016-BUNIBSi016-C 2021-07-00 2021-07-00 PubMed: 34182252 DOI: 10.1016/j.scr.2021.102430Associated cell lines:
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Houweling PJ, Coles CA, Tiong CF, Nielsen B, Graham A, McDonald P, Suter A, Piers AT, Forbes R, Ryan MM, Howden SE, Lamandé SR, North KN
Generating an iPSC line (with isogenic control) from the PBMCs of an ACTA1 (p.Gly148Asp) nemaline myopathy patient
Houweling PJ et al. Generating an iPSC line (with isogenic control) from the PBMCs of an ACTA1 (p.Gly148Asp) nemaline myopathy patient. . 2021-07-00. Pubmed ID: 34157503; DOI: 10.1016/j.scr.2021.102429 MCRIi024-AMCRIi024-A-1 2021-07-00 2021-07-00 PubMed: 34157503 DOI: 10.1016/j.scr.2021.102429Associated cell lines:
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Shuvalova LD, Davidenko AV, Eremeev AV, Khomyakova EA, Zerkalenkova EA, Lebedeva OS, Bogomazova AN, Klyushnikov SA, Illarioshkin SN, Lagarkova MA
Generation of induced pluripotent stem cell line RCPCMi008-A derived from patient with spinocerebellar ataxia 17
Shuvalova LD et al. Generation of induced pluripotent stem cell line RCPCMi008-A derived from patient with spinocerebellar ataxia 17. . 2021-07-00. Pubmed ID: 34171784; DOI: 10.1016/j.scr.2021.102431 RCPCMi008-A 2021-07-00 2021-07-00 PubMed: 34171784 DOI: 10.1016/j.scr.2021.102431Associated cell lines:
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Getachew A, Yang Z, Huang X, Wu F, Liu YY, Yan C, Yang F, Li Y
Generation of a TLR2 homozygous knockout human embryonic stem cell line WAe001-A-64 using CRISPR/Cas9 editing
Getachew A et al. Generation of a TLR2 homozygous knockout human embryonic stem cell line WAe001-A-64 using CRISPR/Cas9 editing. . 2021-07-00. Pubmed ID: 34058685; DOI: 10.1016/j.scr.2021.102401 WAe001-AWAe001-A-64 2021-07-00 2021-07-00 PubMed: 34058685 DOI: 10.1016/j.scr.2021.102401Associated cell lines:
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Tsai MH, Chiu YT, Chan DZ, Wen CH, Syu SH, Lu HE, Huang CF, Lin YJ, Chang SL, Lo LW, Huang CY, Hu YF, Hsieh PCH, Chen SA
Generation of IBMS-iPSC-021, -022, -023 human induced pluripotent stem cells (IBMSi016-A, IBMSi017-A, and IBMSi018-A) derived from patients with the ALDH2 rs671 polymorphism
Tsai MH et al. Generation of IBMS-iPSC-021, -022, -023 human induced pluripotent stem cells (IBMSi016-A, IBMSi017-A, and IBMSi018-A) derived from patients with the ALDH2 rs671 polymorphism. . 2021-07-00. Pubmed ID: 34118567; DOI: 10.1016/j.scr.2021.102416 IBMSi016-AIBMSi017-AIBMSi018-A 2021-07-00 2021-07-00 PubMed: 34118567 DOI: 10.1016/j.scr.2021.102416Associated cell lines:
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Schinke C, Fernandez Vallone V, Ivanov A, Peng Y, Körtvelyessy P, Nolte L, Huehnchen P, Beule D, Stachelscheid H, Boehmerle W, Endres M
Modeling chemotherapy induced neurotoxicity with human induced pluripotent stem cell (iPSC) -derived sensory neurons
Schinke C et al. Modeling chemotherapy induced neurotoxicity with human induced pluripotent stem cell (iPSC) -derived sensory neurons. . 2021-07-00. Pubmed ID: 33984509; DOI: 10.1016/j.nbd.2021.105391 BIHi002-A 2021-07-00 2021-07-00 PubMed: 33984509 DOI: 10.1016/j.nbd.2021.105391Associated cell lines:
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Ababneh NA, Barham R, Al-Kurdi B, Ali D, Sharar N, Al Hadidi S, Alatoom RM, Zalloum S, Gharandouq MH, Makahleh L, Alnsour LN, Alshahwan H, El-Khateeb M, Awidi A
Generation of an induced pluripotent stem cell (iPSC) line (JUCTCi017-A) from a patient with limb-girdle muscular dystrophy (LGMD) due to a homozygous p.Lue287Ser fs14* mutation in the SGCB gene
Ababneh NA et al. Generation of an induced pluripotent stem cell (iPSC) line (JUCTCi017-A) from a patient with limb-girdle muscular dystrophy (LGMD) due to a homozygous p.Lue287Ser fs14* mutation in the SGCB gene. . 2021-07-00. Pubmed ID: 34087734; DOI: 10.1016/j.scr.2021.102358 JUCTCi001-AJUCTCi017-A 2021-07-00 2021-07-00 PubMed: 34087734 DOI: 10.1016/j.scr.2021.102358Associated cell lines:
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Moon SY, Zhang D, Chen SC, Lamey TM, Thompson JA, McLaren TL, De Roach JN, Chen FK, McLenachan S
Generation of two induced pluripotent stem cell lines from a retinitis pigmentosa patient with compound heterozygous mutations in CRB1
Moon SY et al. Generation of two induced pluripotent stem cell lines from a retinitis pigmentosa patient with compound heterozygous mutations in CRB1. . 2021-07-00. Pubmed ID: 34034222; DOI: 10.1016/j.scr.2021.102403 LEIi016-ALEIi016-B 2021-07-00 2021-07-00 PubMed: 34034222 DOI: 10.1016/j.scr.2021.102403 -
Manstein F, Ullmann K, Kropp C, Halloin C, Triebert W, Franke A, Farr CM, Sahabian A, Haase A, Breitkreuz Y, Peitz M, Brüstle O, Kalies S, Martin U, Olmer R, Zweigerdt R
High density bioprocessing of human pluripotent stem cells by metabolic control and in silico modeling
Manstein F et al. High density bioprocessing of human pluripotent stem cells by metabolic control and in silico modeling. . 2021-07-00. Pubmed ID: 33660952; DOI: 10.1002/sctm.20-0453; PMC: PMC8235132 MHHi001-AMHHi006-AMHHi008-A 2021-07-00 2021-07-00 PubMed: 33660952 DOI: 10.1002/sctm.20-0453 -
Dykxhoorn DM, Tong X, Gosstola NC, Liu XZ
Derivation of iPSC line UMi029-A bearing a hearing-loss associated variant in the SMPX gene
Dykxhoorn DM et al. Derivation of iPSC line UMi029-A bearing a hearing-loss associated variant in the SMPX gene. . 2021-07-00. Pubmed ID: 34052664; DOI: 10.1016/j.scr.2021.102405 UMi029-A 2021-07-00 2021-07-00 PubMed: 34052664 DOI: 10.1016/j.scr.2021.102405Associated cell lines:
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Nazish I, Arber C, Piers TM, Warner TT, Hardy JA, Lewis PA, Pocock JM, Bandopadhyay R
Abrogation of LRRK2 dependent Rab10 phosphorylation with TLR4 activation and alterations in evoked cytokine release in immune cells
Nazish I et al. Abrogation of LRRK2 dependent Rab10 phosphorylation with TLR4 activation and alterations in evoked cytokine release in immune cells. . 2021-07-00. Pubmed ID: 34004238; DOI: 10.1016/j.neuint.2021.105070; PMC: PMC7610942 BIONi010-C 2021-07-00 2021-07-00 PubMed: 34004238 DOI: 10.1016/j.neuint.2021.105070Associated cell lines:
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Yang J, Samal E, Burgos Angulo M, Bertalovitz A, McDonald TV
Establishment of an arrhythmogenic right ventricular cardiomyopathy derived iPSC cell line (USFi004-A) carrying a heterozygous mutation in PKP2 (c.1799delA)
Yang J et al. Establishment of an arrhythmogenic right ventricular cardiomyopathy derived iPSC cell line (USFi004-A) carrying a heterozygous mutation in PKP2 (c.1799delA). . 2021-07-00. Pubmed ID: 34034221; DOI: 10.1016/j.scr.2021.102398 USFi004-A 2021-07-00 2021-07-00 PubMed: 34034221 DOI: 10.1016/j.scr.2021.102398Associated cell lines:
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Mollo N, Esposito M, Aurilia M, Scognamiglio R, Accarino R, Bonfiglio F, Cicatiello R, Charalambous M, Procaccini C, Micillo T, Genesio R, Calì G, Secondo A, Paladino S, Matarese G, De Vita G, Conti A, Nitsch L, Izzo A
Human Trisomic iPSCs from Down Syndrome Fibroblasts Manifest Mitochondrial Alterations Early during Neuronal Differentiation
Mollo N et al. Human Trisomic iPSCs from Down Syndrome Fibroblasts Manifest Mitochondrial Alterations Early during Neuronal Differentiation. . 2021-06-30. Pubmed ID: 34209429; DOI: 10.3390/biology10070609; PMC: PMC8301075 UNINAi001-AUNINAi002-A 2021-06-30 2021-06-30 PubMed: 34209429 DOI: 10.3390/biology10070609Associated cell lines:
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Ma X, Ma J, Guo R, Du J, Feng B, Liu X, Du X, Ma Z, Cui H
Blood-derived integration-free induced pluripotent stem cells (iPSCs) from one 53-years-old male donor with APOE-ε4/ε4 genotype
Ma X et al. Blood-derived integration-free induced pluripotent stem cells (iPSCs) from one 53-years-old male donor with APOE-ε4/ε4 genotype. . 2021-07-00. Pubmed ID: 34218115; DOI: 10.1016/j.scr.2021.102450 HEBHMUi001-AHEBHMUi009-A 2021-07-00 2021-07-00 PubMed: 34218115 DOI: 10.1016/j.scr.2021.102450Associated cell lines:
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Brooks BM, Pradhan M, Cheng YS, Gorshkov K, Farkhondeh A, Chen CZ, Beers J, Liu C, Baumgaertel K, Rodems S, Zheng W
Generation of an induced pluripotent stem cell line (TRNDi031-A) from a patient with Alagille syndrome type 1 carrying a heterozygous p. C312X (c. 936 T > A) mutation in JAGGED-1
Brooks BM et al. Generation of an induced pluripotent stem cell line (TRNDi031-A) from a patient with Alagille syndrome type 1 carrying a heterozygous p. C312X (c. 936 T > A) mutation in JAGGED-1. . 2021-07-00. Pubmed ID: 34198154; DOI: 10.1016/j.scr.2021.102447; PMC: PMC8300001 TRNDi031-A 2021-07-00 2021-07-00 PubMed: 34198154 DOI: 10.1016/j.scr.2021.102447Associated cell lines:
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Yan R, Wu S, Wang W, Chu M, Liu P
Generation of a human induced pluripotent stem cell line (SMUSHi001-A) from a patient with 46, XX male sex reversal syndrome carrying the SRY gene
Yan R et al. Generation of a human induced pluripotent stem cell line (SMUSHi001-A) from a patient with 46, XX male sex reversal syndrome carrying the SRY gene. . 2021-07-00. Pubmed ID: 34098200; DOI: 10.1016/j.scr.2021.102397 SMUSHi001-A 2021-07-00 2021-07-00 PubMed: 34098200 DOI: 10.1016/j.scr.2021.102397Associated cell lines:
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Iannello G, Patel A, Sirabella D, Corneo B, Thaker V
Generation of the iPSC line CUIMCi003-A derived from a patient with severe early onset obesity
Iannello G et al. Generation of the iPSC line CUIMCi003-A derived from a patient with severe early onset obesity. . 2021-07-00. Pubmed ID: 34214899; DOI: 10.1016/j.scr.2021.102432; PMC: PMC8340056 CUIMCi002-ACUIMCi003-ACUIMCi003-A-1 2021-07-00 2021-07-00 PubMed: 34214899 DOI: 10.1016/j.scr.2021.102432Associated cell lines:
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Pradhan M, Farkhondeh A, Cheng YS, Xu M, Beers J, Zou J, Liu C, Might M, Rodems S, Baumgärtel K, Zheng W
An induced pluripotent stem cell line (NCATS-CL9075) from a patient carrying compound heterozygote mutations, p.R390P and p.L318P, in the NGLY1 gene
Pradhan M et al. An induced pluripotent stem cell line (NCATS-CL9075) from a patient carrying compound heterozygote mutations, p.R390P and p.L318P, in the NGLY1 gene. . 2021-07-00. Pubmed ID: 34051448; DOI: 10.1016/j.scr.2021.102400; PMC: PMC8362228 TRNDi002-BTRNDi018-C 2021-07-00 2021-07-00 PubMed: 34051448 DOI: 10.1016/j.scr.2021.102400Associated cell lines:
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Borsoi J, Morato-Marques M, de Araújo Tofoli F, Assis Pereira L, Farinha-Arcieri LE, Delgado Sarafian R, Alvarez Perez AB, Veiga Pereira L
Generation of two human induced pluripotent stem cell (hiPSC) lines derived from unrelated Marfan Syndrome patients
Borsoi J et al. Generation of two human induced pluripotent stem cell (hiPSC) lines derived from unrelated Marfan Syndrome patients. . 2021-07-00. Pubmed ID: 34062330; DOI: 10.1016/j.scr.2021.102407 LANCEi021-ALANCEi022-A 2021-07-00 2021-07-00 PubMed: 34062330 DOI: 10.1016/j.scr.2021.102407Associated cell lines:
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Huang D, Zhang D, Chen SC, Aung-Htut MT, Lamey TM, Thompson JA, McLaren TL, De Roach JN, Fletcher S, Wilton SD, Chen FK, McLenachan S
Generation of two induced pluripotent stem cell lines from a patient with Stargardt disease caused by compound heterozygous mutations in the ABCA4 gene
Huang D et al. Generation of two induced pluripotent stem cell lines from a patient with Stargardt disease caused by compound heterozygous mutations in the ABCA4 gene. . 2021-07-00. Pubmed ID: 34198153; DOI: 10.1016/j.scr.2021.102448 LEIi017-ALEIi017-B 2021-07-00 2021-07-00 PubMed: 34198153 DOI: 10.1016/j.scr.2021.102448 -
Svobodova B, Jelinkova S, Pesl M, Beckerová D, Lacampagne A, Meli AC, Rotrekl V
Cellular pathology of the human heart in Duchenne muscular dystrophy (DMD): lessons learned from in vitro modeling
Svobodova B et al. Cellular pathology of the human heart in Duchenne muscular dystrophy (DMD): lessons learned from in vitro modeling. . 2021-07-00. Pubmed ID: 34169350; DOI: 10.1007/s00424-021-02589-0 MUNIi001-AMUNIi003-A 2021-07-00 2021-07-00 PubMed: 34169350 DOI: 10.1007/s00424-021-02589-0Associated cell lines:
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Kawase E, Takada K, Nakatani R, Yamazaki S, Suemori H
Generation of clinical-grade human embryonic stem cell line KthES11 according to Japanese regulations
Kawase E et al. Generation of clinical-grade human embryonic stem cell line KthES11 according to Japanese regulations. . 2021-07-00. Pubmed ID: 34126558; DOI: 10.1016/j.scr.2021.102383 KUIMSe004-A 2021-07-00 2021-07-00 PubMed: 34126558 DOI: 10.1016/j.scr.2021.102383Associated cell lines:
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Meraviglia V, Ganesh S, Arendzen CH, Freund C, Sommariva E, Rossini A, Bellin M
Generation of human induced pluripotent stem cell line EURACi006-A and its isogenic gene-corrected line EURACi006-A-1 from an arrhythmogenic cardiomyopathy patient carrying the c.1643delG PKP2 mutation
Meraviglia V et al. Generation of human induced pluripotent stem cell line EURACi006-A and its isogenic gene-corrected line EURACi006-A-1 from an arrhythmogenic cardiomyopathy patient carrying the c.1643delG PKP2 mutation. . 2021-07-00. Pubmed ID: 34134068; DOI: 10.1016/j.scr.2021.102426 EURACi006-AEURACi006-A-1 2021-07-00 2021-07-00 PubMed: 34134068 DOI: 10.1016/j.scr.2021.102426Associated cell lines:
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Angulo MB, Yang J, Argenziano MA, Bertalovitz AC, Beidokhti MN, McDonald TV
Generation of a Friedreich's Ataxia patient-derived iPSC line USFi001-A
Angulo MB et al. Generation of a Friedreich's Ataxia patient-derived iPSC line USFi001-A. . 2021-07-00. Pubmed ID: 34034220; DOI: 10.1016/j.scr.2021.102399 USFi001-A 2021-07-00 2021-07-00 PubMed: 34034220 DOI: 10.1016/j.scr.2021.102399Associated cell lines:
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Mondéjar-Parreño G, Jahng JWS, Belbachir N, Wu BC, Zhang X, Perez MV, Badhwar N, Wu JC
Generation of three heterozygous KCNH2 mutation-carrying human induced pluripotent stem cell lines for modeling LQT2 syndrome
Mondéjar-Parreño G et al. Generation of three heterozygous KCNH2 mutation-carrying human induced pluripotent stem cell lines for modeling LQT2 syndrome. . 2021-07-00. Pubmed ID: 34051449; DOI: 10.1016/j.scr.2021.102402; PMC: PMC10875632 SCVIi001-ASCVIi002-ASCVIi009-ASCVIi010-ASCVIi011-A 2021-07-00 2021-07-00 PubMed: 34051449 DOI: 10.1016/j.scr.2021.102402Associated cell lines:
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Huang D, Zhang D, Chen SC, Thandar Aung-Htut M, Lamey TM, Thompson JA, McLaren TL, De Roach JN, Fletcher S, Wilton SD, McLenachan S, Chen FK
Generation of an induced pluripotent stem cell line from a patient with Stargardt disease caused by biallelic c.[5461-10T>C;5603A>T];[6077T>C] mutations in the ABCA4 gene
Huang D et al. Generation of an induced pluripotent stem cell line from a patient with Stargardt disease caused by biallelic c.[5461-10T>C;5603A>T];[6077T>C] mutations in the ABCA4 gene. . 2021-07-00. Pubmed ID: 34214897; DOI: 10.1016/j.scr.2021.102439 LEIi018-A 2021-07-00 2021-07-00 PubMed: 34214897 DOI: 10.1016/j.scr.2021.102439Associated cell lines:
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Son D, Zheng J, Kim IY, You S
Self-replicative mRNA-mediated generation of induced pluripotent stem cell line from a 1-year-old Leigh syndrome patient with mitochondrial DNA cytochrome b mutation
Son D et al. Self-replicative mRNA-mediated generation of induced pluripotent stem cell line from a 1-year-old Leigh syndrome patient with mitochondrial DNA cytochrome b mutation. . 2021-07-00. Pubmed ID: 34091428; DOI: 10.1016/j.scr.2021.102392 KUCFRi003-A 2021-07-00 2021-07-00 PubMed: 34091428 DOI: 10.1016/j.scr.2021.102392Associated cell lines:
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Pandolfi EC, Hunt TJ, Goldsmith S, Hurlbut K, Silber SJ, Clark AT
Generation of three human induced pluripotent stem cell sublines (UCLAi004-A, UCLAi004-B, and UCLAi004-C) for reproductive science research
Pandolfi EC et al. Generation of three human induced pluripotent stem cell sublines (UCLAi004-A, UCLAi004-B, and UCLAi004-C) for reproductive science research. . 2021-07-00. Pubmed ID: 34216981; DOI: 10.1016/j.scr.2021.102446; PMC: PMC9354709 UCLAi004-AUCLAi004-BUCLAi004-C 2021-07-00 2021-07-00 PubMed: 34216981 DOI: 10.1016/j.scr.2021.102446Associated cell lines:
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Pandolfi EC, Hunt TJ, Goldsmith S, Hurlbut K, Silber SJ, Clark AT
Generation of three human induced pluripotent stem cell sublines (UCLAi005-A, UCLAi005-B and UCLAi005-C) for reproductive science research
Pandolfi EC et al. Generation of three human induced pluripotent stem cell sublines (UCLAi005-A, UCLAi005-B and UCLAi005-C) for reproductive science research. . 2021-07-00. Pubmed ID: 34130154; DOI: 10.1016/j.scr.2021.102409; PMC: PMC9411073 UCLAi005-AUCLAi005-BUCLAi005-C 2021-07-00 2021-07-00 PubMed: 34130154 DOI: 10.1016/j.scr.2021.102409Associated cell lines:
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Quan Y, Jin P, Ma J, Yang J, Wang Z, Zhang H, Hu M, Fan J, Fan X, Gong Y, Li M, Wang Y
Generation of human embryonic stem cell lines (WAe001-A-67,WAe001-A-68) with TEAD1 and TEAD4 expression by the PiggyBac transposon system
Quan Y et al. Generation of human embryonic stem cell lines (WAe001-A-67,WAe001-A-68) with TEAD1 and TEAD4 expression by the PiggyBac transposon system. . 2021-07-00. Pubmed ID: 34058684; DOI: 10.1016/j.scr.2021.102408 WAe001-AWMUi001-AWAe001-A-47WAe001-A-67WAe001-A-68 2021-07-00 2021-07-00 PubMed: 34058684 DOI: 10.1016/j.scr.2021.102408Associated cell lines:
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Fu Q, Wang H, Zhou N, Jiang Y, Liang Y, Duan F, Mi L
Generation of a human iPSC line from a Bardet-Biedl syndrome patient compound heterozygous for the BBS7 variants c.849 + 1G > C/c.754G > A
Fu Q et al. Generation of a human iPSC line from a Bardet-Biedl syndrome patient compound heterozygous for the BBS7 variants c.849 + 1G > C/c.754G > A. . 2021-07-00. Pubmed ID: 34146953; DOI: 10.1016/j.scr.2021.102428 BCHNi001-A 2021-07-00 2021-07-00 PubMed: 34146953 DOI: 10.1016/j.scr.2021.102428Associated cell lines:
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Wu S, Zhang Z, Wang L, Yu J
Generation of a human iPSC line QDMHi001-A from a patient with Marfan syndrome carrying a heterozygous c.6772 T > C variant in FBN1
Wu S et al. Generation of a human iPSC line QDMHi001-A from a patient with Marfan syndrome carrying a heterozygous c.6772 T > C variant in FBN1. . 2021-07-00. Pubmed ID: 34087733; DOI: 10.1016/j.scr.2021.102390 CIBi007-AQDMHi001-A 2021-07-00 2021-07-00 PubMed: 34087733 DOI: 10.1016/j.scr.2021.102390Associated cell lines:
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Huang PS, Wen MH, Xie X, Xu A, Lee DF, Chen TY
Generation of a homozygous knock-in human embryonic stem cell line expressing SNAP-tagged SOD1
Huang PS et al. Generation of a homozygous knock-in human embryonic stem cell line expressing SNAP-tagged SOD1. . 2021-07-00. Pubmed ID: 34118566; DOI: 10.1016/j.scr.2021.102415; PMC: PMC8330834 WAe001-AWAe001-A-56 2021-07-00 2021-07-00 PubMed: 34118566 DOI: 10.1016/j.scr.2021.102415Associated cell lines:
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Mathieu C, Bovier FT, Ferren M, Lieberman NAP, Predella C, Lalande A, Peddu V, Lin MJ, Addetia A, Patel A, Outlaw V, Corneo B, Dorrello NV, Briese T, Hardie D, Horvat B, Moscona A, Greninger AL, Porotto M
Molecular Features of the Measles Virus Viral Fusion Complex That Favor Infection and Spread in the Brain
Mathieu C et al. Molecular Features of the Measles Virus Viral Fusion Complex That Favor Infection and Spread in the Brain. . 2021-06-29. Pubmed ID: 34061592; DOI: 10.1128/mbio.00799-21; PMC: PMC8263006 CUIMCi001-ACUIMCi002-A 2021-06-29 2021-06-29 PubMed: 34061592 DOI: 10.1128/mbio.00799-21Associated cell lines:
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Morais Mychel Raony Paiva Teixeira, Tian Pinyuan, Lawless Craig, Murtuza-Baker Syed, Hopkinson Louise, Woods Steven, Mironov Aleksandr, Long David Andrew, Gale Daniel, Zorn Telma Maria Tenorio, Kimber Susan, Zent Roy, Lennon Rachel
Kidney organoids: A system to study human basement membrane assembly in health and disease
Morais Mychel Raony Paiva Teixeira et al. Kidney organoids: A system to study human basement membrane assembly in health and disease. . 2021-06-29. DOI: 10.1101/2021.06.27.450067 WTSIi503-AWTSIi519-AWTSIi623-A 2021-06-29 2021-06-29 DOI: 10.1101/2021.06.27.450067Associated cell lines:
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Wißfeld J, Mathews M, Mossad O, Picardi P, Cinti A, Redaelli L, Pradier L, Brüstle O, Neumann H
Reporter cell assay for human CD33 validated by specific antibodies and human iPSC-derived microglia
Wißfeld J et al. Reporter cell assay for human CD33 validated by specific antibodies and human iPSC-derived microglia. . 2021-06-29. Pubmed ID: 34188106; DOI: 10.1038/s41598-021-92434-2; PMC: PMC8242067 BIONi010-CBIONi010-C-5BIONi010-C-9 2021-06-29 2021-06-29 PubMed: 34188106 DOI: 10.1038/s41598-021-92434-2Associated cell lines:
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Amponsah AE, Guo R, Kong D, Feng B, He J, Zhang W, Liu X, Du X, Ma Z, Liu B, Ma J, Cui H
Patient-derived iPSCs, a reliable in vitro model for the investigation of Alzheimer's disease
Amponsah AE et al. Patient-derived iPSCs, a reliable in vitro model for the investigation of Alzheimer's disease. . 2021-06-25. Pubmed ID: 33550785; DOI: 10.1515/revneuro-2020-0065 HEBHMUi001-A 2021-06-25 2021-06-25 PubMed: 33550785 DOI: 10.1515/revneuro-2020-0065Associated cell lines:
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Cosker K, Mallach A, Limaye J, Piers TM, Staddon J, Neame SJ, Hardy J, Pocock JM
Microglial signalling pathway deficits associated with the patient derived R47H TREM2 variants linked to AD indicate inability to activate inflammasome
Cosker K et al. Microglial signalling pathway deficits associated with the patient derived R47H TREM2 variants linked to AD indicate inability to activate inflammasome. . 2021-06-25. Pubmed ID: 34172778; DOI: 10.1038/s41598-021-91207-1; PMC: PMC8233372 BIONi010-C 2021-06-25 2021-06-25 PubMed: 34172778 DOI: 10.1038/s41598-021-91207-1Associated cell lines:
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Borziak K, Parvanova I, Finkelstein J
ReMeDy: a platform for integrating and sharing published stem cell research data with a focus on iPSC trials
Borziak K et al. ReMeDy: a platform for integrating and sharing published stem cell research data with a focus on iPSC trials. . 2021-06-22. Pubmed ID: 34156448; DOI: 10.1093/database/baab038; PMC: PMC8218701 KUMCi002-A 2021-06-22 2021-06-22 PubMed: 34156448 DOI: 10.1093/database/baab038Associated cell lines:
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Bandaru S, Ala C, Zhou AX, Akyürek LM
Filamin A Regulates Cardiovascular Remodeling
Bandaru S et al. Filamin A Regulates Cardiovascular Remodeling. . 2021-06-18. Pubmed ID: 34207234; DOI: 10.3390/ijms22126555; PMC: PMC8235345 ZZUNEUi008-A 2021-06-18 2021-06-18 PubMed: 34207234 DOI: 10.3390/ijms22126555Associated cell lines:
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Wszoła M, Nitarska D, Cywoniuk P, Gomółka M, Klak M
Stem Cells as a Source of Pancreatic Cells for Production of 3D Bioprinted Bionic Pancreas in the Treatment of Type 1 Diabetes
Wszoła M et al. Stem Cells as a Source of Pancreatic Cells for Production of 3D Bioprinted Bionic Pancreas in the Treatment of Type 1 Diabetes. . 2021-06-18. Pubmed ID: 34207441; DOI: 10.3390/cells10061544; PMC: PMC8234129 ICGi002-AICGi002-BICGi002-C 2021-06-18 2021-06-18 PubMed: 34207441 DOI: 10.3390/cells10061544 -
Richardson SE, Ghazanfari R, Chhetri J, Enver T, Böiers C
In vitro differentiation of human pluripotent stem cells into the B lineage using OP9-MS5 co-culture
Richardson SE et al. In vitro differentiation of human pluripotent stem cells into the B lineage using OP9-MS5 co-culture. . 2021-06-18. Pubmed ID: 33899010; DOI: 10.1016/j.xpro.2021.100420; PMC: PMC8053808 WAe001-AUOSi001-AUOSi001-B 2021-06-18 2021-06-18 PubMed: 33899010 DOI: 10.1016/j.xpro.2021.100420 -
Vigh JP, Kincses A, Ozgür B, Walter FR, Santa-Maria AR, Valkai S, Vastag M, Neuhaus W, Brodin B, Dér A, Deli MA
Transendothelial Electrical Resistance Measurement across the Blood-Brain Barrier: A Critical Review of Methods
Vigh JP et al. Transendothelial Electrical Resistance Measurement across the Blood-Brain Barrier: A Critical Review of Methods. . 2021-06-11. Pubmed ID: 34208338; DOI: 10.3390/mi12060685; PMC: PMC8231150 BIONi010-C 2021-06-11 2021-06-11 PubMed: 34208338 DOI: 10.3390/mi12060685Associated cell lines:
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Hofbauer P, Jahnel SM, Papai N, Giesshammer M, Deyett A, Schmidt C, Penc M, Tavernini K, Grdseloff N, Meledeth C, Ginistrelli LC, Ctortecka C, Šalic Š, Novatchkova M, Mendjan S
Cardioids reveal self-organizing principles of human cardiogenesis
Hofbauer P et al. Cardioids reveal self-organizing principles of human cardiogenesis. . 2021-06-10. Pubmed ID: 34019794; DOI: 10.1016/j.cell.2021.04.034 UCSFi001-AUCSFi001-A-3UCSFi001-A-11UCSFi001-A-26UCSFi001-A-27UCSFi001-A-29UCSFi001-A-30UCSFi001-A-32IMBAi001-AIMBAi002-AIMBAi003-A 2021-06-10 2021-06-10 PubMed: 34019794 DOI: 10.1016/j.cell.2021.04.034Associated cell lines:
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Bathe-Peters M, Gmach P, Boltz HH, Einsiedel J, Gotthardt M, Hübner H, Gmeiner P, Lohse MJ, Annibale P
Visualization of β-adrenergic receptor dynamics and differential localization in cardiomyocytes
Bathe-Peters M et al. Visualization of β-adrenergic receptor dynamics and differential localization in cardiomyocytes. . 2021-06-08. Pubmed ID: 34088840; DOI: 10.1073/pnas.2101119118; PMC: PMC8201832 BIHi005-A 2021-06-08 2021-06-08 PubMed: 34088840 DOI: 10.1073/pnas.2101119118Associated cell lines:
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Mitsuzawa S, Suzuki N, Akiyama T, Ishikawa M, Sone T, Kawada J, Funayama R, Shirota M, Mitsuhashi H, Morimoto S, Ikeda K, Shijo T, Ohno A, Nakamura N, Ono H, Ono R, Osana S, Nakagawa T, Nishiyama A, Izumi R, Kaneda S, Ikeuchi Y, Nakayama K, Fujii T, Warita H, Okano H, Aoki M
Reduced PHOX2B stability causes axonal growth impairment in motor neurons with TARDBP mutations
Mitsuzawa S et al. Reduced PHOX2B stability causes axonal growth impairment in motor neurons with TARDBP mutations. . 2021-06-08. Pubmed ID: 34048688; DOI: 10.1016/j.stemcr.2021.04.021; PMC: PMC8190591 KEIOi001-A 2021-06-08 2021-06-08 PubMed: 34048688 DOI: 10.1016/j.stemcr.2021.04.021Associated cell lines:
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Guo G, Stirparo GG, Strawbridge SE, Spindlow D, Yang J, Clarke J, Dattani A, Yanagida A, Li MA, Myers S, Özel BN, Nichols J, Smith A
Human naive epiblast cells possess unrestricted lineage potential
Guo G et al. Human naive epiblast cells possess unrestricted lineage potential. . 2021-06-03. Pubmed ID: 33831366; DOI: 10.1016/j.stem.2021.02.025; PMC: PMC8189439 CAMe001-A 2021-06-03 2021-06-03 PubMed: 33831366 DOI: 10.1016/j.stem.2021.02.025Associated cell lines:
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Di Buduo CA, Laurent PA, Zaninetti C, Lordier L, Soprano PM, Ntai A, Barozzi S, La Spada A, Biunno I, Raslova H, Bussel JB, Kaplan DL, Balduini CL, Pecci A, Balduini A
Miniaturized 3D bone marrow tissue model to assess response to Thrombopoietin-receptor agonists in patients
Di Buduo CA et al. Miniaturized 3D bone marrow tissue model to assess response to Thrombopoietin-receptor agonists in patients. . 2021-06-01. Pubmed ID: 34059198; DOI: 10.7554/elife.58775; PMC: PMC8169123 RCe021-AMUi010-A 2021-06-01 2021-06-01 PubMed: 34059198 DOI: 10.7554/elife.58775 -
Liang W.
Application value of genetic screening for hereditary deafness in universal newborn hearing screening
Liang W.. Application value of genetic screening for hereditary deafness in universal newborn hearing screening. . 2021-06-01. DOI: 10.7683/xxyxyxb.2021.06.015 JUFMDOi004-A 2021-06-01 2021-06-01 DOI: 10.7683/xxyxyxb.2021.06.015Associated cell lines:
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Vigh J, Kincses A, Ozgür B, Walter F, Santa-Maria A, Valkai S, Vastag M, Neuhaus W, Brodin B, Dér A, Deli M.
Transendothelial Electrical Resistance Measurement across the Blood–Brain Barrier: A Critical Review of Methods
Vigh J et al. Transendothelial Electrical Resistance Measurement across the Blood–Brain Barrier: A Critical Review of Methods. . 2021-06-01. BIONi010-C 2021-06-01 2021-06-01Associated cell lines:
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Sadeqi Nezhad M, Abdollahpour-Alitappeh M, Rezaei B, Yazdanifar M, Seifalian AM
Induced Pluripotent Stem Cells (iPSCs) Provide a Potentially Unlimited T Cell Source for CAR-T Cell Development and Off-the-Shelf Products
Sadeqi Nezhad M et al. Induced Pluripotent Stem Cells (iPSCs) Provide a Potentially Unlimited T Cell Source for CAR-T Cell Development and Off-the-Shelf Products. . 2021-06-00. Pubmed ID: 34114161; DOI: 10.1007/s11095-021-03067-z MUSIi011-AMUSIi011-B 2021-06-00 2021-06-00 PubMed: 34114161 DOI: 10.1007/s11095-021-03067-zAssociated cell lines:
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Zaaijer S, Groen SC, Sanjana NE
Tracking cell lineages to improve research reproducibility
Zaaijer S et al. Tracking cell lineages to improve research reproducibility. . 2021-06-00. Pubmed ID: 34012093; DOI: 10.1038/s41587-021-00928-1; PMC: PMC9644290 NYGCe001-A 2021-06-00 2021-06-00 PubMed: 34012093 DOI: 10.1038/s41587-021-00928-1Associated cell lines:
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Wißfeld J, Nozaki I, Mathews M, Raschka T, Ebeling C, Hornung V, Brüstle O, Neumann H
Deletion of Alzheimer's disease-associated CD33 results in an inflammatory human microglia phenotype
Wißfeld J et al. Deletion of Alzheimer's disease-associated CD33 results in an inflammatory human microglia phenotype. . 2021-06-00. Pubmed ID: 33539598; DOI: 10.1002/glia.23968 BIONi010-C-5BIONi010-C-9 2021-06-00 2021-06-00 PubMed: 33539598 DOI: 10.1002/glia.23968Associated cell lines:
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Song S, Ashok A, Williams D, Kaufman M, Duff K, Sproul A
Efficient Derivation of Excitatory and Inhibitory Neurons from Human Pluripotent Stem Cells Stably Expressing Direct Reprogramming Factors
Song S et al. Efficient Derivation of Excitatory and Inhibitory Neurons from Human Pluripotent Stem Cells Stably Expressing Direct Reprogramming Factors. . 2021-06-00. Pubmed ID: 34102035; DOI: 10.1002/cpz1.141; PMC: PMC8191582 FRIMOi003-AFRIMOi004-A 2021-06-00 2021-06-00 PubMed: 34102035 DOI: 10.1002/cpz1.141Associated cell lines:
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Salmina AB, Komleva YK, Malinovskaya NA, Morgun AV, Teplyashina EA, Lopatina OL, Gorina YV, Kharitonova EV, Khilazheva ED, Shuvaev AN
Blood-Brain Barrier Breakdown in Stress and Neurodegeneration: Biochemical Mechanisms and New Models for Translational Research
Salmina AB et al. Blood-Brain Barrier Breakdown in Stress and Neurodegeneration: Biochemical Mechanisms and New Models for Translational Research. . 2021-06-00. Pubmed ID: 34225598; DOI: 10.1134/s0006297921060122 BIONi010-C 2021-06-00 2021-06-00 PubMed: 34225598 DOI: 10.1134/s0006297921060122Associated cell lines:
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Sun Lingyu, Zhu Xiyu, Zhang Xiaoxuan, Chen Guopu, Bian Feika, Wang Junxia, Zhou Qing, Wang Dongjin, Zhao Yuanjin
Induced cardiomyocytes-integrated conductive microneedle patch for treating myocardial infarction
Sun Lingyu et al. Induced cardiomyocytes-integrated conductive microneedle patch for treating myocardial infarction. . 2021-06-00. DOI: 10.1016/j.cej.2021.128723 NJDTHi001-A 2021-06-00 2021-06-00 DOI: 10.1016/j.cej.2021.128723Associated cell lines:
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Hinca SB, Salcedo C, Wagner A, Goldeman C, Sadat E, Aibar MMD, Maechler P, Brodin B, Aldana BI, Helms HCC
Brain endothelial cells metabolize glutamate via glutamate dehydrogenase to replenish TCA-intermediates and produce ATP under hypoglycemic conditions
Hinca SB et al. Brain endothelial cells metabolize glutamate via glutamate dehydrogenase to replenish TCA-intermediates and produce ATP under hypoglycemic conditions. . 2021-06-00. Pubmed ID: 33025588; DOI: 10.1111/jnc.15207 BIONi010-C 2021-06-00 2021-06-00 PubMed: 33025588 DOI: 10.1111/jnc.15207Associated cell lines:
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Hildebrandt S, Kampfrath B, Fischer K, Hildebrand L, Haupt J, Stachelscheid H, Knaus P
ActivinA Induced SMAD1/5 Signaling in an iPSC Derived EC Model of Fibrodysplasia Ossificans Progressiva (FOP) Can Be Rescued by the Drug Candidate Saracatinib
Hildebrandt S et al. ActivinA Induced SMAD1/5 Signaling in an iPSC Derived EC Model of Fibrodysplasia Ossificans Progressiva (FOP) Can Be Rescued by the Drug Candidate Saracatinib. . 2021-06-00. Pubmed ID: 33410098; DOI: 10.1007/s12015-020-10103-9; PMC: PMC8166717 BCRTi001-ABCRTi002-ABCRTi004-ABCRTi005-A 2021-06-00 2021-06-00 PubMed: 33410098 DOI: 10.1007/s12015-020-10103-9Associated cell lines:
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Manini A, Pantoni L
CADASIL from Bench to Bedside: Disease Models and Novel Therapeutic Approaches
Manini A et al. CADASIL from Bench to Bedside: Disease Models and Novel Therapeutic Approaches. . 2021-06-00. Pubmed ID: 33464533; DOI: 10.1007/s12035-021-02282-4; PMC: PMC8128844 IDISi001-A 2021-06-00 2021-06-00 PubMed: 33464533 DOI: 10.1007/s12035-021-02282-4Associated cell lines:
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Pushp P, Nogueira DES, Rodrigues CAV, Ferreira FC, Cabral JMS, Gupta MK
A Concise Review on Induced Pluripotent Stem Cell-Derived Cardiomyocytes for Personalized Regenerative Medicine
Pushp P et al. A Concise Review on Induced Pluripotent Stem Cell-Derived Cardiomyocytes for Personalized Regenerative Medicine. . 2021-06-00. Pubmed ID: 33098306; DOI: 10.1007/s12015-020-10061-2 CSSi007-AINMi003-AUAMi005-ANUIGi022-ANUIGi023-AIRFMNi003-ANUIGi024-ANUIGi025-ANUIGi026-AIRFMNi003-A-1IRFMNi003-A-2NUIGi022-BNUIGi024-BNUIGi025-BNUIGi026-BNUIGi023-BICGi014-AHEBHMUi002-AMMCi001-ASKLOi001-A 2021-06-00 2021-06-00 PubMed: 33098306 DOI: 10.1007/s12015-020-10061-2 -
Alari V, Scalmani P, Ajmone PF, Perego S, Avignone S, Catusi I, Lonati PA, Borghi MO, Finelli P, Terragni B, Mantegazza M, Russo S, Larizza L
Histone Deacetylase Inhibitors Ameliorate Morphological Defects and Hypoexcitability of iPSC-Neurons from Rubinstein-Taybi Patients
Alari V et al. Histone Deacetylase Inhibitors Ameliorate Morphological Defects and Hypoexcitability of iPSC-Neurons from Rubinstein-Taybi Patients. . 2021-05-28. Pubmed ID: 34071322; DOI: 10.3390/ijms22115777; PMC: PMC8197986 IAIi002-AIAIi004-A 2021-05-28 2021-05-28 PubMed: 34071322 DOI: 10.3390/ijms22115777 -
Golunova A, Velychkivska N, Mikšovská Z, Chochola V, Jaroš J, Hampl A, Pop-Georgievski O, Proks V
Direct and Indirect Biomimetic Peptide Modification of Alginate: Efficiency, Side Reactions, and Cell Response
Golunova A et al. Direct and Indirect Biomimetic Peptide Modification of Alginate: Efficiency, Side Reactions, and Cell Response. . 2021-05-27. Pubmed ID: 34072085; DOI: 10.3390/ijms22115731; PMC: PMC8198284 MUNIe007-A 2021-05-27 2021-05-27 PubMed: 34072085 DOI: 10.3390/ijms22115731Associated cell lines:
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Low BSJ, Lim CS, Ding SSL, Tan YS, Ng NHJ, Krishnan VG, Ang SF, Neo CWY, Verma CS, Hoon S, Lim SC, Tai ES, Teo AKK
Decreased GLUT2 and glucose uptake contribute to insulin secretion defects in MODY3/HNF1A hiPSC-derived mutant β cells
Low BSJ et al. Decreased GLUT2 and glucose uptake contribute to insulin secretion defects in MODY3/HNF1A hiPSC-derived mutant β cells. . 2021-05-25. Pubmed ID: 34035238; DOI: 10.1038/s41467-021-22843-4; PMC: PMC8149827 ATLABi001-AATLABi002-A 2021-05-25 2021-05-25 PubMed: 34035238 DOI: 10.1038/s41467-021-22843-4Associated cell lines:
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Liu X, Lillywhite J, Zhu W, Huang Z, Clark AM, Gosstola N, Maguire CT, Dykxhoorn D, Chen ZY, Yang J
Generation and Genetic Correction of USH2A c.2299delG Mutation in Patient-Derived Induced Pluripotent Stem Cells
Liu X et al. Generation and Genetic Correction of USH2A c.2299delG Mutation in Patient-Derived Induced Pluripotent Stem Cells. . 2021-05-25. Pubmed ID: 34070435; DOI: 10.3390/genes12060805; PMC: PMC8227183 IISHDOi004-AINMi001-AINMi002-AFRIMOi002-AUMi028-AUMi028-A-1 2021-05-25 2021-05-25 PubMed: 34070435 DOI: 10.3390/genes12060805Associated cell lines:
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Wanke F, Gutbier S, Rümmelin A, Steinberg M, Hughes LD, Koenen M, Komuczki J, Regan-Komito D, Wagage S, Hesselmann J, Thoma R, Brugger D, Christopeit T, Wang H, Point F, Hallet R, Ghosh S, Rothlin CV, Patsch C, Geering B
Ligand-dependent kinase activity of MERTK drives efferocytosis in human iPSC-derived macrophages
Wanke F et al. Ligand-dependent kinase activity of MERTK drives efferocytosis in human iPSC-derived macrophages. . 2021-05-25. Pubmed ID: 34035216; DOI: 10.1038/s41419-021-03770-0; PMC: PMC8149813 STBCi026-B 2021-05-25 2021-05-25 PubMed: 34035216 DOI: 10.1038/s41419-021-03770-0Associated cell lines:
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Escobar H, Krause A, Keiper S, Kieshauer J, Müthel S, de Paredes MG, Metzler E, Kühn R, Heyd F, Spuler S
Base editing repairs an SGCA mutation in human primary muscle stem cells
Escobar H et al. Base editing repairs an SGCA mutation in human primary muscle stem cells. . 2021-05-24. Pubmed ID: 33848270; DOI: 10.1172/jci.insight.145994; PMC: PMC8262330 MDCi014-AMDCi014-BMDCi017-A 2021-05-24 2021-05-24 PubMed: 33848270 DOI: 10.1172/jci.insight.145994 -
Naik S, Wood AR, Ongenaert M, Saidiyan P, Elstak ED, Lanz HL, Stallen J, Janssen R, Smythe E, Erdmann KS
A 3D Renal Proximal Tubule on Chip Model Phenocopies Lowe Syndrome and Dent II Disease Tubulopathy
Naik S et al. A 3D Renal Proximal Tubule on Chip Model Phenocopies Lowe Syndrome and Dent II Disease Tubulopathy. . 2021-05-19. Pubmed ID: 34069732; DOI: 10.3390/ijms22105361; PMC: PMC8161077 SDUBMSi009-A 2021-05-19 2021-05-19 PubMed: 34069732 DOI: 10.3390/ijms22105361Associated cell lines:
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Kessi M, Chen B, Peng J, Yan F, Yang L, Yin F
Calcium channelopathies and intellectual disability: a systematic review
Kessi M et al. Calcium channelopathies and intellectual disability: a systematic review. . 2021-05-13. Pubmed ID: 33985586; DOI: 10.1186/s13023-021-01850-0; PMC: PMC8120735 SHEHi002-A 2021-05-13 2021-05-13 PubMed: 33985586 DOI: 10.1186/s13023-021-01850-0Associated cell lines:
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Shi T, Cheung M
Urine-derived induced pluripotent/neural stem cells for modeling neurological diseases
Shi T et al. Urine-derived induced pluripotent/neural stem cells for modeling neurological diseases. . 2021-05-13. Pubmed ID: 33985584; DOI: 10.1186/s13578-021-00594-5; PMC: PMC8117626 SYSUi001-A 2021-05-13 2021-05-13 PubMed: 33985584 DOI: 10.1186/s13578-021-00594-5Associated cell lines:
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Poon A, Saini H, Sethi S, O'Sullivan GA, Plun-Favreau H, Wray S, Dawson LA, McCarthy JM
The role of SQSTM1 (p62) in mitochondrial function and clearance in human cortical neurons
Poon A et al. The role of SQSTM1 (p62) in mitochondrial function and clearance in human cortical neurons. . 2021-05-11. Pubmed ID: 33891871; DOI: 10.1016/j.stemcr.2021.03.030; PMC: PMC8185463 RBi001-AUOXFi005-A 2021-05-11 2021-05-11 PubMed: 33891871 DOI: 10.1016/j.stemcr.2021.03.030Associated cell lines:
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Fus-Kujawa A, Mendrek B, Trybus A, Bajdak-Rusinek K, Stepien KL, Sieron AL
Potential of Induced Pluripotent Stem Cells for Use in Gene Therapy: History, Molecular Bases, and Medical Perspectives
Fus-Kujawa A et al. Potential of Induced Pluripotent Stem Cells for Use in Gene Therapy: History, Molecular Bases, and Medical Perspectives. . 2021-05-07. Pubmed ID: 34067183; DOI: 10.3390/biom11050699; PMC: PMC8151405 MCRIi001-AMCRIi001-A-1 2021-05-07 2021-05-07 PubMed: 34067183 DOI: 10.3390/biom11050699Associated cell lines:
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Kour S, Rajan DS, Fortuna TR, Anderson EN, Ward C, Lee Y, Lee S, Shin YB, Chae JH, Choi M, Siquier K, Cantagrel V, Amiel J, Stolerman ES, Barnett SS, Cousin MA, Castro D, McDonald K, Kirmse B, Nemeth AH, Rajasundaram D, Innes AM, Lynch D, Frosk P, Collins A, Gibbons M, Yang M, Desguerre I, Boddaert N, Gitiaux C, Rydning SL, Selmer KK, Urreizti R, Garcia-Oguiza A, Osorio AN, Verdura E, Pujol A, McCurry HR, Landers JE, Agnihotri S, Andriescu EC, Moody SB, Phornphutkul C, Sacoto MJG, Begtrup A, Houlden H, Kirschner J, Schorling D, Rudnik-Schöneborn S, Strom TM, Leiz S, Juliette K, Richardson R, Yang Y, Zhang Y, Wang M, Wang J, Wang X, Platzer K, Donkervoort S, Bönnemann CG, Wagner M, Issa MY, Elbendary HM, Stanley V, Maroofian R, Gleeson JG, Zaki MS, Senderek J, Pandey UB
Loss of function mutations in GEMIN5 cause a neurodevelopmental disorder
Kour S et al. Loss of function mutations in GEMIN5 cause a neurodevelopmental disorder. . 2021-05-07. Pubmed ID: 33963192; DOI: 10.1038/s41467-021-22627-w; PMC: PMC8105379 TUSMi008-A 2021-05-07 2021-05-07 PubMed: 33963192 DOI: 10.1038/s41467-021-22627-wAssociated cell lines:
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Pettinato AM, Yoo D, VanOudenhove J, Chen YS, Cohn R, Ladha FA, Yang X, Thakar K, Romano R, Legere N, Meredith E, Robson P, Regnier M, Cotney JL, Murry CE, Hinson JT
Sarcomere function activates a p53-dependent DNA damage response that promotes polyploidization and limits in vivo cell engraftment
Pettinato AM et al. Sarcomere function activates a p53-dependent DNA damage response that promotes polyploidization and limits in vivo cell engraftment. . 2021-05-04. Pubmed ID: 33951429; DOI: 10.1016/j.celrep.2021.109088; PMC: PMC8161465 UCSFi001-A 2021-05-04 2021-05-04 PubMed: 33951429 DOI: 10.1016/j.celrep.2021.109088Associated cell lines:
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James OG, Selvaraj BT, Magnani D, Burr K, Connick P, Barton SK, Vasistha NA, Hampton DW, Story D, Smigiel R, Ploski R, Brophy PJ, Ffrench-Constant C, Lyons DA, Chandran S
iPSC-derived myelinoids to study myelin biology of humans
James OG et al. iPSC-derived myelinoids to study myelin biology of humans. . 2021-05-03. Pubmed ID: 33945785; DOI: 10.1016/j.devcel.2021.04.006; PMC: PMC8098746 AXORe004-A 2021-05-03 2021-05-03 PubMed: 33945785 DOI: 10.1016/j.devcel.2021.04.006Associated cell lines:
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Woo MS, Ufer F, Rothammer N, Di Liberto G, Binkle L, Haferkamp U, Sonner JK, Engler JB, Hornig S, Bauer S, Wagner I, Egervari K, Raber J, Duvoisin RM, Pless O, Merkler D, Friese MA
Neuronal metabotropic glutamate receptor 8 protects against neurodegeneration in CNS inflammation
Woo MS et al. Neuronal metabotropic glutamate receptor 8 protects against neurodegeneration in CNS inflammation. . 2021-05-03. Pubmed ID: 33661276; DOI: 10.1084/jem.20201290; PMC: PMC7938362 ZIPi013-B 2021-05-03 2021-05-03 PubMed: 33661276 DOI: 10.1084/jem.20201290Associated cell lines:
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Gnecchi M, Sala L, Schwartz PJ
Precision Medicine and cardiac channelopathies: when dreams meet reality
Gnecchi M et al. Precision Medicine and cardiac channelopathies: when dreams meet reality. . 2021-05-01. Pubmed ID: 33686390; DOI: 10.1093/eurheartj/ehab007; PMC: PMC8088342 PSMi003-A 2021-05-01 2021-05-01 PubMed: 33686390 DOI: 10.1093/eurheartj/ehab007Associated cell lines:
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García-López M.
Research progress in mitochondrial dynamics and gene abnormalities related to hereditary optic neuropathy
García-López M.. Research progress in mitochondrial dynamics and gene abnormalities related to hereditary optic neuropathy. . 2021-05-01. DOI: 10.13481/j.1671-587x.20210333 FINCBi001-A 2021-05-01 2021-05-01 DOI: 10.13481/j.1671-587x.20210333Associated cell lines:
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Penna S, Villa A, Capo V
Autosomal recessive osteopetrosis: mechanisms and treatments
Penna S et al. Autosomal recessive osteopetrosis: mechanisms and treatments. . 2021-05-01. Pubmed ID: 33970241; DOI: 10.1242/dmm.048940; PMC: PMC8188884 BIHi002-A 2021-05-01 2021-05-01 PubMed: 33970241 DOI: 10.1242/dmm.048940Associated cell lines:
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You J, Cheng Y, Yang XJ, Chen L
Generation of a homozygous LRP2 knockout human embryonic stem cell line (FDCHDPe010-A-56) by CRISPR/Cas9 system
You J et al. Generation of a homozygous LRP2 knockout human embryonic stem cell line (FDCHDPe010-A-56) by CRISPR/Cas9 system. . 2021-05-00. Pubmed ID: 33878707; DOI: 10.1016/j.scr.2021.102342; PMC: PMC9303849 WAe009-A-56 2021-05-00 2021-05-00 PubMed: 33878707 DOI: 10.1016/j.scr.2021.102342Associated cell lines:
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Dong L, Zhang H, Quan Y, Jin P, Yang J, Fan X, Fan J, Li M, Gong Y, Wang Y
Establishment and characterization of human induced pluripotent stem cell line (WMUi020-A) from a patient with bicuspid aortic valve aortopathy
Dong L et al. Establishment and characterization of human induced pluripotent stem cell line (WMUi020-A) from a patient with bicuspid aortic valve aortopathy. . 2021-05-00. Pubmed ID: 33631418; DOI: 10.1016/j.scr.2021.102260 WMUi001-AWMUi020-A 2021-05-00 2021-05-00 PubMed: 33631418 DOI: 10.1016/j.scr.2021.102260 -
Cañibano-Hernández A, Valdes-Sanchez L, Garcia-Delgado AB, Ponte-Zúñiga B, Diaz-Corrales FJ, de la Cerda B
Generation of the human iPSC line ESi082-A from a patient with macular dystrophy associated to mutations in the CRB1 gene
Cañibano-Hernández A et al. Generation of the human iPSC line ESi082-A from a patient with macular dystrophy associated to mutations in the CRB1 gene. . 2021-05-00. Pubmed ID: 33773389; DOI: 10.1016/j.scr.2021.102301 ESi082-A 2021-05-00 2021-05-00 PubMed: 33773389 DOI: 10.1016/j.scr.2021.102301Associated cell lines:
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Ma Y, Wang Z, Gao M, Liu X, Sun W, Gong Y, Sun G, Liu G
Generation of two induced pluripotent stem cell lines from patients with X-linked Alport syndrome
Ma Y et al. Generation of two induced pluripotent stem cell lines from patients with X-linked Alport syndrome. . 2021-05-00. Pubmed ID: 33878711; DOI: 10.1016/j.scr.2021.102343 SDUBMSi007-ASDUBMSi008-A 2021-05-00 2021-05-00 PubMed: 33878711 DOI: 10.1016/j.scr.2021.102343Associated cell lines:
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Ye L, Yu Y, Wang Y, Huang Y, Yu M, Lei W, Tang JM, Hu S
Establishment and characterization of a human embryonic stem cell line carrying a heterozygous GATA4(T280M) mutation
Ye L et al. Establishment and characterization of a human embryonic stem cell line carrying a heterozygous GATA4(T280M) mutation. . 2021-05-00. Pubmed ID: 34088018; DOI: 10.1016/j.scr.2021.102393 WAe007-A-1 2021-05-00 2021-05-00 PubMed: 34088018 DOI: 10.1016/j.scr.2021.102393Associated cell lines:
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Brooks BM, Yeh CD, Beers J, Liu C, Cheng YS, Gorshkov K, Zou J, Zheng W, Chen CZ
Generation of an induced pluripotent stem cell line (TRNDi030-A) from a patient with Farber disease carrying a homozygous p. Y36C (c. 107 A>G) mutation in ASAH1
Brooks BM et al. Generation of an induced pluripotent stem cell line (TRNDi030-A) from a patient with Farber disease carrying a homozygous p. Y36C (c. 107 A>G) mutation in ASAH1. . 2021-05-00. Pubmed ID: 34088014; DOI: 10.1016/j.scr.2021.102387; PMC: PMC8314383 TRNDi030-A 2021-05-00 2021-05-00 PubMed: 34088014 DOI: 10.1016/j.scr.2021.102387Associated cell lines:
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Wu H, Cheng Y, Lv Z, Liu L, Gong W, Zhang S
Characterization of human induced pluripotent stem cells line JLUEYEi002-A from a 48 year old healthy male
Wu H et al. Characterization of human induced pluripotent stem cells line JLUEYEi002-A from a 48 year old healthy male. . 2021-05-00. Pubmed ID: 33677395; DOI: 10.1016/j.scr.2021.102221 JLUEYEi002-A 2021-05-00 2021-05-00 PubMed: 33677395 DOI: 10.1016/j.scr.2021.102221Associated cell lines:
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Sun C, Li B, Yang M, Guo R, Yuan S, Wang J, Hu H
Generation of GPAM knockout human embryonic stem cell line SYSUe-008-A using CRISPR/Cas9
Sun C et al. Generation of GPAM knockout human embryonic stem cell line SYSUe-008-A using CRISPR/Cas9. . 2021-05-00. Pubmed ID: 33831647; DOI: 10.1016/j.scr.2021.102303 SYSUe008-A 2021-05-00 2021-05-00 PubMed: 33831647 DOI: 10.1016/j.scr.2021.102303Associated cell lines:
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Qian R, Wang L, Chen H, Ding Y, Wang D, Chen C, Chu M, Shan X, Guo X
Establishment of a human induced pluripotent stem cell line (WMUi031-A) from a Lowe syndrome patient carrying a OCRL gene mutation (c.2626dupA)
Qian R et al. Establishment of a human induced pluripotent stem cell line (WMUi031-A) from a Lowe syndrome patient carrying a OCRL gene mutation (c.2626dupA). . 2021-05-00. Pubmed ID: 33765594; DOI: 10.1016/j.scr.2021.102294 WMUi031-A 2021-05-00 2021-05-00 PubMed: 33765594 DOI: 10.1016/j.scr.2021.102294Associated cell lines:
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Beylina A, Langston RG, Rosen D, Reed X, Cookson MR
Generation of fourteen isogenic cell lines for Parkinson's disease-associated leucine-rich repeat kinase (LRRK2)
Beylina A et al. Generation of fourteen isogenic cell lines for Parkinson's disease-associated leucine-rich repeat kinase (LRRK2). . 2021-05-00. Pubmed ID: 34087985; DOI: 10.1016/j.scr.2021.102354; PMC: PMC8314873 TMOi001-ANIAi001-ANIAi001-BNIAi001-CNIAi001-DNIAi001-ENIAi001-FNIAi001-GNIAi001-HNIAi001-INIAi001-JNIAi001-KNIAi001-LNIAi001-MNIAi001-N 2021-05-00 2021-05-00 PubMed: 34087985 DOI: 10.1016/j.scr.2021.102354 -
Tsukamoto S, Nakade K, Wakabayashi T, Nakashima K, Takami M, Hemmi Y, Kuramochi Y, Shimizu T, Arai Y, Matsuo-Takasaki M, Noguchi M, Nakamura Y, Miwa Y, Hayashi Y
Generation of two ISL1-tdTomato reporter human induced pluripotent stem cell lines using CRISPR-Cas9 genome editing
Tsukamoto S et al. Generation of two ISL1-tdTomato reporter human induced pluripotent stem cell lines using CRISPR-Cas9 genome editing. . 2021-05-00. Pubmed ID: 34087992; DOI: 10.1016/j.scr.2021.102363 BRCi014-ABRCi014-A-1BRCi014-A-2 2021-05-00 2021-05-00 PubMed: 34087992 DOI: 10.1016/j.scr.2021.102363Associated cell lines:
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Li J, Wu K, Guan J, Wang Q, Wang H
Generation of a human induced pluripotent stem cell line (CPGHi003-A) from an auditory neuropathy patient with AIFM1 p.R422Q mutation
Li J et al. Generation of a human induced pluripotent stem cell line (CPGHi003-A) from an auditory neuropathy patient with AIFM1 p.R422Q mutation. . 2021-05-00. Pubmed ID: 34088005; DOI: 10.1016/j.scr.2021.102376 CPGHi003-A 2021-05-00 2021-05-00 PubMed: 34088005 DOI: 10.1016/j.scr.2021.102376Associated cell lines:
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Raska J, Hribkova H, Klimova H, Fedorova V, Barak M, Barta T, Pospisilova V, Vochyanova S, Vanova T, Bohaciakova D
Generation of six human iPSC lines from patients with a familial Alzheimer's disease (n = 3) and sex- and age-matched healthy controls (n = 3)
Raska J et al. Generation of six human iPSC lines from patients with a familial Alzheimer's disease (n = 3) and sex- and age-matched healthy controls (n = 3). . 2021-05-00. Pubmed ID: 34088008; DOI: 10.1016/j.scr.2021.102379 MUNIi005-AMUNIi006-AMUNIi007-AMUNIi008-AMUNIi009-AMUNIi010-A 2021-05-00 2021-05-00 PubMed: 34088008 DOI: 10.1016/j.scr.2021.102379Associated cell lines:
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He L, Han X, Zhao H, Li S, Chen Z, Wang C, Wang S, Peng L, Deng W, Li Z, Tang B, Jiang H
Generation of spinocerebellar ataxia type 3 patient-derived induced pluripotent stem cell line (CSUXHi005-A) from human urine epithelial cells
He L et al. Generation of spinocerebellar ataxia type 3 patient-derived induced pluripotent stem cell line (CSUXHi005-A) from human urine epithelial cells. . 2021-05-00. Pubmed ID: 33761381; DOI: 10.1016/j.scr.2021.102289 CSUXHi001-ACSUXHi002-ACSUXHi005-A 2021-05-00 2021-05-00 PubMed: 33761381 DOI: 10.1016/j.scr.2021.102289Associated cell lines:
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Wang X, Zhang M, Guo R, Liu X, Du X, Liu B, Ma Z, Ma J, Cui H
Derivation of induced pluripotent stem cells from one child suffering Potocki-Lupski syndrome
Wang X et al. Derivation of induced pluripotent stem cells from one child suffering Potocki-Lupski syndrome. . 2021-05-00. Pubmed ID: 33839548; DOI: 10.1016/j.scr.2021.102324 DHMCi005-A 2021-05-00 2021-05-00 PubMed: 33839548 DOI: 10.1016/j.scr.2021.102324Associated cell lines:
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Wang L, Zhao H, Wu J, Ren J, Luo H, Zuo X, Chen Q, Tang Y
An induced pluripotent stem cell line (CSUi004-A) from skin fibroblasts of a healthy individual
Wang L et al. An induced pluripotent stem cell line (CSUi004-A) from skin fibroblasts of a healthy individual. . 2021-05-00. Pubmed ID: 33865102; DOI: 10.1016/j.scr.2021.102336 CSUi002-ACSUi004-A 2021-05-00 2021-05-00 PubMed: 33865102 DOI: 10.1016/j.scr.2021.102336 -
Lauschke K, Treschow AF, Rasmussen MA, Davidsen N, Holst B, Emnéus J, Taxvig C, Vinggaard AM
Creating a human-induced pluripotent stem cell-based NKX2.5 reporter gene assay for developmental toxicity testing
Lauschke K et al. Creating a human-induced pluripotent stem cell-based NKX2.5 reporter gene assay for developmental toxicity testing. . 2021-05-00. Pubmed ID: 33660062; DOI: 10.1007/s00204-021-03018-y; PMC: PMC8113199 BIONi010-C 2021-05-00 2021-05-00 PubMed: 33660062 DOI: 10.1007/s00204-021-03018-yAssociated cell lines:
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Fukunaga I, Oe Y, Danzaki K, Ohta S, Chen C, Iizumi M, Shiga T, Matsuoka R, Anzai T, Hibiya-Motegi R, Tajima S, Ikeda K, Akamatsu W, Kamiya K
Generation of two iPSC lines from siblings of a homozygous patient with hearing loss and a heterozygous carrier with normal hearing carrying p.G45E/Y136X mutation in GJB2
Fukunaga I et al. Generation of two iPSC lines from siblings of a homozygous patient with hearing loss and a heterozygous carrier with normal hearing carrying p.G45E/Y136X mutation in GJB2. . 2021-05-00. Pubmed ID: 33780732; DOI: 10.1016/j.scr.2021.102290 JUFMDOi001-AJUFMDOi002-A 2021-05-00 2021-05-00 PubMed: 33780732 DOI: 10.1016/j.scr.2021.102290Associated cell lines:
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Zhang XH, Xie Y, Xu K, Li Y
Generation of an induced pluripotent stem cell line BIOi002-A from a patient with autosomal dominant optic atrophy
Zhang XH et al. Generation of an induced pluripotent stem cell line BIOi002-A from a patient with autosomal dominant optic atrophy. . 2021-05-00. Pubmed ID: 33752025; DOI: 10.1016/j.scr.2021.102278 BIOi002-A 2021-05-00 2021-05-00 PubMed: 33752025 DOI: 10.1016/j.scr.2021.102278Associated cell lines:
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Pichard L, Brondello JM, Becker F, Desprat R, De Ceuninck F, Pastoureau P, Noel D, Jorgensen C, Lemaitre JM
Establishment of a collection of human pluripotent stem cell lines (iPSC) from mesenchymal stem cells (MSC) from three healthy elderly donors
Pichard L et al. Establishment of a collection of human pluripotent stem cell lines (iPSC) from mesenchymal stem cells (MSC) from three healthy elderly donors. . 2021-05-00. Pubmed ID: 33780731; DOI: 10.1016/j.scr.2021.102297 REGUi012-AREGUi013-AREGUi014-A 2021-05-00 2021-05-00 PubMed: 33780731 DOI: 10.1016/j.scr.2021.102297Associated cell lines:
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Ding Y, O'Brien A, Marcó de la Cruz B, Yang M, Lu Y, Qian X, Yang G, McInerney V, Krawczyk J, Lynch SA, Howard L, Allen NM, O'Brien T, Gallagher L, Shen S
Derivation of four iPSC lines from a male ASD patient carrying a deletion in the middle coding region of NRXN1α gene (NUIGi039-A and NUIGi039-B) and a male sibling control (NUIGi040-A and NUIGi040-B)
Ding Y et al. Derivation of four iPSC lines from a male ASD patient carrying a deletion in the middle coding region of NRXN1α gene (NUIGi039-A and NUIGi039-B) and a male sibling control (NUIGi040-A and NUIGi040-B). . 2021-05-00. Pubmed ID: 33631419; DOI: 10.1016/j.scr.2021.102254 NUIGi039-ANUIGi040-ANUIGi039-BNUIGi040-B 2021-05-00 2021-05-00 PubMed: 33631419 DOI: 10.1016/j.scr.2021.102254Associated cell lines:
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Kondrateva E, Demchenko A, Slesarenko Y, Yasinovsky M, Amelina E, Tabakov V, Voronina E, Lavrov A, Smirnikhina S
Derivation of iPSC line (RCMGi002-A) from dermal fibroblasts of a cystic fibrosis female patient with homozygous F508del mutation
Kondrateva E et al. Derivation of iPSC line (RCMGi002-A) from dermal fibroblasts of a cystic fibrosis female patient with homozygous F508del mutation. . 2021-05-00. Pubmed ID: 33684631; DOI: 10.1016/j.scr.2021.102251 RCMGi002-A 2021-05-00 2021-05-00 PubMed: 33684631 DOI: 10.1016/j.scr.2021.102251Associated cell lines:
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Clayton JS, Scriba CK, Romero NB, Malfatti E, Saker S, Larmonier T, Nowak KJ, Ravenscroft G, Laing NG, Taylor RL
Generation of two isogenic induced pluripotent stem cell lines from a 4-month-old severe nemaline myopathy patient with a heterozygous dominant c.553C > A (p.Arg183Ser) variant in the ACTA1 gene
Clayton JS et al. Generation of two isogenic induced pluripotent stem cell lines from a 4-month-old severe nemaline myopathy patient with a heterozygous dominant c.553C > A (p.Arg183Ser) variant in the ACTA1 gene. . 2021-05-00. Pubmed ID: 33740643; DOI: 10.1016/j.scr.2021.102273 HPIi001-AHPIi001-B 2021-05-00 2021-05-00 PubMed: 33740643 DOI: 10.1016/j.scr.2021.102273 -
Zhu W, Cheng YS, Xu M, Farkhondeh A, Beers J, Zou J, Liu C, Baumgaertel K, Rodems S, Zheng W
Generation of Alagille syndrome derived induced pluripotent stem cell line carrying heterozygous mutation in the JAGGED-1 gene at splicing site (Chr20: 10,629,709C>A) before exon 11
Zhu W et al. Generation of Alagille syndrome derived induced pluripotent stem cell line carrying heterozygous mutation in the JAGGED-1 gene at splicing site (Chr20: 10,629,709C>A) before exon 11. . 2021-05-00. Pubmed ID: 34087995; DOI: 10.1016/j.scr.2021.102366; PMC: PMC9482691 TRNDi029-A 2021-05-00 2021-05-00 PubMed: 34087995 DOI: 10.1016/j.scr.2021.102366Associated cell lines:
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Guo X, Qian R, Shan X, Yang L, Chen H, Ding Y, Chen C, Chu M, Lin J, Wang D
Generation of a human induced pluripotent stem cell line (WMUi021-A) from a Gitelman syndrome patient carrying a SLC12A3 gene mutation (c.179C > T)
Guo X et al. Generation of a human induced pluripotent stem cell line (WMUi021-A) from a Gitelman syndrome patient carrying a SLC12A3 gene mutation (c.179C > T). . 2021-05-00. Pubmed ID: 33735743; DOI: 10.1016/j.scr.2021.102280 WMUi021-A 2021-05-00 2021-05-00 PubMed: 33735743 DOI: 10.1016/j.scr.2021.102280Associated cell lines:
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Wu H, Wang G, Gao E, Zhao J, Zhang L, Chen L, Zhu Y, Zhang J, Liu Z
Generation of the induced pluripotent stem cell line (NCKDi002-A) from a 22-year-old patient with Focal Segmental Glomerular Sclerosis carrying a heterozygous mutation in WT1 gene
Wu H et al. Generation of the induced pluripotent stem cell line (NCKDi002-A) from a 22-year-old patient with Focal Segmental Glomerular Sclerosis carrying a heterozygous mutation in WT1 gene. . 2021-05-00. Pubmed ID: 33780729; DOI: 10.1016/j.scr.2021.102293 NCKDi002-A 2021-05-00 2021-05-00 PubMed: 33780729 DOI: 10.1016/j.scr.2021.102293Associated cell lines:
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Devito LG, Healy L, Mohammed S, Guillemot F, Dias C
Generation of an iPSC line (CRICKi001-A) from an individual with a germline SMARCA4 missense mutation and autism spectrum disorder
Devito LG et al. Generation of an iPSC line (CRICKi001-A) from an individual with a germline SMARCA4 missense mutation and autism spectrum disorder. . 2021-05-00. Pubmed ID: 33799280; DOI: 10.1016/j.scr.2021.102304; PMC: PMC8164104 KCLi001-ACRICKi001-A 2021-05-00 2021-05-00 PubMed: 33799280 DOI: 10.1016/j.scr.2021.102304Associated cell lines:
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Gong T, Wang H, Huang B, Wang H, Zhang P, Qian J
Reprogramming of human peripheral blood mononuclear cells from a patient suffering from recurrent hydatidiform mole to an iPSC line FAHZUi001-A carrying a homozygous p.Gln421Ter mutation in NLRP7 gene
Gong T et al. Reprogramming of human peripheral blood mononuclear cells from a patient suffering from recurrent hydatidiform mole to an iPSC line FAHZUi001-A carrying a homozygous p.Gln421Ter mutation in NLRP7 gene. . 2021-05-00. Pubmed ID: 34087990; DOI: 10.1016/j.scr.2021.102361 FAHZUi001-A 2021-05-00 2021-05-00 PubMed: 34087990 DOI: 10.1016/j.scr.2021.102361Associated cell lines:
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Kim JH, Jo HY, Ha HY, Kim YO
Korea National Stem Cell Bank
Kim JH et al. Korea National Stem Cell Bank. . 2021-05-00. Pubmed ID: 33714852; DOI: 10.1016/j.scr.2021.102270 SNUe003-ASNUe004-AKSCBi001-AKSCBi002-AKSCBi002-BKSCBi002-B-1KSCBi003-AKSCBi005-AKSCBi005-A-1KSCBi005-A-3KSCBi010-AKSCBi011-AKSCBi002-A-1KSCBi012-ASNUe007-AKSCBi017-AKSCBi018-AKSCBi019-AKSCBi020-AKSCBi002-A-2KSCBi021-A 2021-05-00 2021-05-00 PubMed: 33714852 DOI: 10.1016/j.scr.2021.102270 -
Guo G, Fu W, Li X, Dong J, Zhao X, Zhang Y
Generation of an iPSC line (ZZUNEUi016-A) derived from a hypertrophic cardiomyopathy patient with the heterozygote mutation in MYH7 gene
Guo G et al. Generation of an iPSC line (ZZUNEUi016-A) derived from a hypertrophic cardiomyopathy patient with the heterozygote mutation in MYH7 gene. . 2021-05-00. Pubmed ID: 33636496; DOI: 10.1016/j.scr.2021.102262 ZZUNEUi016-A 2021-05-00 2021-05-00 PubMed: 33636496 DOI: 10.1016/j.scr.2021.102262Associated cell lines:
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Longobardi E, Miceli F, Secondo A, Cicatiello R, Izzo A, Tinto N, Moutton S, Tran Mau-Them F, Vitobello A, Taglialatela M
Generation of an iPSC line (UNINAi001-A) from a girl with neonatal-onset epilepsy and non-syndromic intellectual disability carrying the homozygous KCNQ3 p.PHE534ILEfs*15 variant and of an iPSC line (UNINAi002-A) from a non-carrier, unaffected brother
Longobardi E et al. Generation of an iPSC line (UNINAi001-A) from a girl with neonatal-onset epilepsy and non-syndromic intellectual disability carrying the homozygous KCNQ3 p.PHE534ILEfs*15 variant and of an iPSC line (UNINAi002-A) from a non-carrier, unaffected brother. . 2021-05-00. Pubmed ID: 33799276; DOI: 10.1016/j.scr.2021.102311 UNINAi001-AUNINAi002-A 2021-05-00 2021-05-00 PubMed: 33799276 DOI: 10.1016/j.scr.2021.102311Associated cell lines:
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Jahng JWS, Black KE, Liu L, Bae HR, Perez M, Ashley EA, Sallam K, Wu JC
Generation of three induced pluripotent stem cell lines, SCVIi003-A, SCVIi004-A, SCVIi005-A, from patients with ARVD/C caused by heterozygous mutations in the PKP2 gene
Jahng JWS et al. Generation of three induced pluripotent stem cell lines, SCVIi003-A, SCVIi004-A, SCVIi005-A, from patients with ARVD/C caused by heterozygous mutations in the PKP2 gene. . 2021-05-00. Pubmed ID: 33743362; DOI: 10.1016/j.scr.2021.102284; PMC: PMC8457924 SCVIi003-ASCVIi004-ASCVIi005-A 2021-05-00 2021-05-00 PubMed: 33743362 DOI: 10.1016/j.scr.2021.102284Associated cell lines:
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Guo R, Mu W, Liu X, Zhang J, Liu B, Du X, He J, Ma J, Cui H
Reprogramming of a human induced pluripotent stem cell line from one 48-year-old healthy male donor
Guo R et al. Reprogramming of a human induced pluripotent stem cell line from one 48-year-old healthy male donor. . 2021-05-00. Pubmed ID: 33892291; DOI: 10.1016/j.scr.2021.102339 DHMCi005-AHEBHMUi001-ASIAISi011-AIGIBi002-AHEBHMUi007-A 2021-05-00 2021-05-00 PubMed: 33892291 DOI: 10.1016/j.scr.2021.102339Associated cell lines:
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Gao X, Li G, Deng H, Feng W, Li Y, Liu M, Li Y
Generation of an iPSC line (GWCMCi002-A) from an X-linked Alport syndrome patient with a hemizygous splicing mutation (NM_000495.4, c. 1517-1 G > T) in the COL4A5 gene
Gao X et al. Generation of an iPSC line (GWCMCi002-A) from an X-linked Alport syndrome patient with a hemizygous splicing mutation (NM_000495.4, c. 1517-1 G > T) in the COL4A5 gene. . 2021-05-00. Pubmed ID: 34088015; DOI: 10.1016/j.scr.2021.102388 GWCMCi002-A 2021-05-00 2021-05-00 PubMed: 34088015 DOI: 10.1016/j.scr.2021.102388Associated cell lines:
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Zhang H, Liu C, Ma Y, Lin L, Lv Y, Gao M, Gai Z, Liu Y
Generation of an induced pluripotent stem cell line SDQLCHi026-A from a hereditary tyrosinemia type I patient carrying compound heterozygote mutations in FAH gene
Zhang H et al. Generation of an induced pluripotent stem cell line SDQLCHi026-A from a hereditary tyrosinemia type I patient carrying compound heterozygote mutations in FAH gene. . 2021-05-00. Pubmed ID: 33882394; DOI: 10.1016/j.scr.2021.102331 SDQLCHi026-A 2021-05-00 2021-05-00 PubMed: 33882394 DOI: 10.1016/j.scr.2021.102331Associated cell lines:
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Machuca C, Correa-Vela M, García-Navas D, Darling A, Villalón-García I, Sánchez-Alcázar JA, Pérez-Dueñas B, Erceg S, Espinós C
Generation of three human iPSC lines from PLAN (PLA2G6-associated neurodegeneration) patients
Machuca C et al. Generation of three human iPSC lines from PLAN (PLA2G6-associated neurodegeneration) patients. . 2021-05-00. Pubmed ID: 34087982; DOI: 10.1016/j.scr.2021.102338 RCPFi004-ARCPFi005-ARCPFi006-A 2021-05-00 2021-05-00 PubMed: 34087982 DOI: 10.1016/j.scr.2021.102338Associated cell lines:
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Li Y, Liu X, Chen D, Liu Y, Ma Y, Liu Q, Sun W, Li J
Generation of an induced pluripotent stem cell line SDUBMSi005-A from a patient with double primary gastric and colon carcinoma
Li Y et al. Generation of an induced pluripotent stem cell line SDUBMSi005-A from a patient with double primary gastric and colon carcinoma. . 2021-05-00. Pubmed ID: 33770698; DOI: 10.1016/j.scr.2021.102253 SDUBMSi005-A 2021-05-00 2021-05-00 PubMed: 33770698 DOI: 10.1016/j.scr.2021.102253Associated cell lines:
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Ramme AP, Faust D, Koenig L, Nguyen N, Marx U
Generation of two additional integration-free iPSC lines from related human donors
Ramme AP et al. Generation of two additional integration-free iPSC lines from related human donors. . 2021-05-00. Pubmed ID: 33901815; DOI: 10.1016/j.scr.2021.102327 TISSUi001-ATISSUi006-ATISSUi007-A 2021-05-00 2021-05-00 PubMed: 33901815 DOI: 10.1016/j.scr.2021.102327Associated cell lines:
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Long F, Liu X, Liu Y, Liu Q, Sun W
An iPS cell line SDUBMSi0011-A from a multiple epiphyseal dysplasia patient carrying c. 1076T > G mutation in the SMOC2 gene
Long F et al. An iPS cell line SDUBMSi0011-A from a multiple epiphyseal dysplasia patient carrying c. 1076T > G mutation in the SMOC2 gene. . 2021-05-00. Pubmed ID: 33892290; DOI: 10.1016/j.scr.2021.102353 SDUBMSi011-A 2021-05-00 2021-05-00 PubMed: 33892290 DOI: 10.1016/j.scr.2021.102353Associated cell lines:
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Luo Q, Wei C, Long Y, Zhang M, Shan W, Li H, Cai S, Xu Y, Qian P, Huang H
Generation of an ELTD1 knockout human embryonic stem cell line by the iCRISPR/Cas9 system
Luo Q et al. Generation of an ELTD1 knockout human embryonic stem cell line by the iCRISPR/Cas9 system. . 2021-05-00. Pubmed ID: 34087984; DOI: 10.1016/j.scr.2021.102350 FAHZUe001-A 2021-05-00 2021-05-00 PubMed: 34087984 DOI: 10.1016/j.scr.2021.102350Associated cell lines:
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Dementyeva EV, Vyatkin YV, Chernyavsky AM, Zakian SM
Generation of an induced pluripotent stem cell line, ICGi028-A, by reprogramming peripheral blood mononuclear cells of a patient suffering from hypertrophic cardiomyopathy and carrying a heterozygous p.E510Q mutation in HADHA
Dementyeva EV et al. Generation of an induced pluripotent stem cell line, ICGi028-A, by reprogramming peripheral blood mononuclear cells of a patient suffering from hypertrophic cardiomyopathy and carrying a heterozygous p.E510Q mutation in HADHA. . 2021-05-00. Pubmed ID: 33887580; DOI: 10.1016/j.scr.2021.102348 ICGi028-A 2021-05-00 2021-05-00 PubMed: 33887580 DOI: 10.1016/j.scr.2021.102348Associated cell lines:
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Dementyeva EV, Pavlova SV, Chernyavsky AM, Zakian SM
Generation of an induced pluripotent stem cell line, ICGi029-A, by reprogramming peripheral blood mononuclear cells of a patient suffering from hypertrophic cardiomyopathy and carrying a heterozygous p.N515del mutation in MYBPC3
Dementyeva EV et al. Generation of an induced pluripotent stem cell line, ICGi029-A, by reprogramming peripheral blood mononuclear cells of a patient suffering from hypertrophic cardiomyopathy and carrying a heterozygous p.N515del mutation in MYBPC3. . 2021-05-00. Pubmed ID: 33892289; DOI: 10.1016/j.scr.2021.102344 ICGi029-A 2021-05-00 2021-05-00 PubMed: 33892289 DOI: 10.1016/j.scr.2021.102344Associated cell lines:
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Liu L, Shenoy SP, Jahng JWS, Liu Y, Knowles JW, Zhuge Y, Wu JC
Generation of two heterozygous MYBPC3 mutation-carrying human iPSC lines, SCVIi001-A and SCVIi002-A, for modeling hypertrophic cardiomyopathy
Liu L et al. Generation of two heterozygous MYBPC3 mutation-carrying human iPSC lines, SCVIi001-A and SCVIi002-A, for modeling hypertrophic cardiomyopathy. . 2021-05-00. Pubmed ID: 33743363; DOI: 10.1016/j.scr.2021.102279; PMC: PMC9393020 SCVIi001-ASCVIi002-A 2021-05-00 2021-05-00 PubMed: 33743363 DOI: 10.1016/j.scr.2021.102279Associated cell lines:
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Kuramochi Y, Awaya T, Matsuo-Takasaki M, Takami M, An Y, Li J, Hemmi Y, Wakabayashi T, Arai Y, Inoue J, Noguchi M, Nakamura Y, Asaka I, Akimoto K, Saito MK, Hayashi Y
Generation of two human induced pluripotent stem cell lines derived from two X-linked adrenoleukodystrophy patients with ABCD1 mutations
Kuramochi Y et al. Generation of two human induced pluripotent stem cell lines derived from two X-linked adrenoleukodystrophy patients with ABCD1 mutations. . 2021-05-00. Pubmed ID: 33901816; DOI: 10.1016/j.scr.2021.102337 BRCi012-ABRCi013-A 2021-05-00 2021-05-00 PubMed: 33901816 DOI: 10.1016/j.scr.2021.102337 -
Janz A, Zink M, Cirnu A, Hartleb A, Albrecht C, Rost S, Klopocki E, Günther K, Edenhofer F, Ergün S, Gerull B
CRISPR/Cas9-edited PKP2 knock-out (JMUi001-A-2) and DSG2 knock-out (JMUi001-A-3) iPSC lines as an isogenic human model system for arrhythmogenic cardiomyopathy (ACM)
Janz A et al. CRISPR/Cas9-edited PKP2 knock-out (JMUi001-A-2) and DSG2 knock-out (JMUi001-A-3) iPSC lines as an isogenic human model system for arrhythmogenic cardiomyopathy (ACM). . 2021-05-00. Pubmed ID: 33640690; DOI: 10.1016/j.scr.2021.102256 JMUi001-AJMUi001-A-2JMUi001-A-3 2021-05-00 2021-05-00 PubMed: 33640690 DOI: 10.1016/j.scr.2021.102256Associated cell lines:
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Raska J, Klimova H, Sheardova K, Fedorova V, Hribkova H, Pospisilova V, Vochyanova S, Vanova T, Bohaciakova D
Generation of three human iPSC lines from patients with a spontaneous late-onset Alzheimer's disease and three sex- and age-matched healthy controls
Raska J et al. Generation of three human iPSC lines from patients with a spontaneous late-onset Alzheimer's disease and three sex- and age-matched healthy controls. . 2021-05-00. Pubmed ID: 34088007; DOI: 10.1016/j.scr.2021.102378 MUNIi011-AMUNIi012-AMUNIi013-AMUNIi014-AMUNIi015-AMUNIi016-A 2021-05-00 2021-05-00 PubMed: 34088007 DOI: 10.1016/j.scr.2021.102378Associated cell lines:
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Jia WW, Lu JZ, Zhang L, Cao HX, Qi YY, Zhu HY, Bai ZH, Zhang SM, Qiao ZB, Bao Y, Liu ZM
An induced pluripotent stem cell line (EHTJUi003-A) generated from a neonate with c.1377delC mutation in the gene MYBPC3 causing hypertrophic cardiomyopathy
Jia WW et al. An induced pluripotent stem cell line (EHTJUi003-A) generated from a neonate with c.1377delC mutation in the gene MYBPC3 causing hypertrophic cardiomyopathy. . 2021-05-00. Pubmed ID: 34087980; DOI: 10.1016/j.scr.2021.102328 EHTJUi003-A 2021-05-00 2021-05-00 PubMed: 34087980 DOI: 10.1016/j.scr.2021.102328Associated cell lines:
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Li N, Lin SM, Li Y, Sun J, Zhang L, Chen M
An induced pluripotent stem cell line (GZHMCi004-A) derived from a fetus with heterozygous G380R mutation in FGFR3 gene causing achondroplasia
Li N et al. An induced pluripotent stem cell line (GZHMCi004-A) derived from a fetus with heterozygous G380R mutation in FGFR3 gene causing achondroplasia. . 2021-05-00. Pubmed ID: 33848795; DOI: 10.1016/j.scr.2021.102322 GZHMCi004-A 2021-05-00 2021-05-00 PubMed: 33848795 DOI: 10.1016/j.scr.2021.102322Associated cell lines:
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Jia N, Gong X, Chen J, Yang T, Bao C, Shen J, Xiao X
Generation of an induced pluripotent stem cell line (OGHFUi001-A) from a type 1 early infantile epileptic encephalopathy with ARX mutation
Jia N et al. Generation of an induced pluripotent stem cell line (OGHFUi001-A) from a type 1 early infantile epileptic encephalopathy with ARX mutation. . 2021-05-00. Pubmed ID: 34087996; DOI: 10.1016/j.scr.2021.102367 OGHFUi001-A 2021-05-00 2021-05-00 PubMed: 34087996 DOI: 10.1016/j.scr.2021.102367Associated cell lines:
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Qi YY, Lu JZ, Zhang L, Cao HX, Zhu HY, Bai ZH, Zhang SM, Qiao ZB, Jia WW, Liu ZM
An induced pluripotent stem cell line (EHTJUi004-A) generated from a neonate with c.4683_4684delCT:p.Leu1563fs mutation in the gene DSP causing Familial Arrhythmogenic Right Ventricular Dysplasia (ARVD)
Qi YY et al. An induced pluripotent stem cell line (EHTJUi004-A) generated from a neonate with c.4683_4684delCT:p.Leu1563fs mutation in the gene DSP causing Familial Arrhythmogenic Right Ventricular Dysplasia (ARVD). . 2021-05-00. Pubmed ID: 34087998; DOI: 10.1016/j.scr.2021.102369 EHTJUi004-A 2021-05-00 2021-05-00 PubMed: 34087998 DOI: 10.1016/j.scr.2021.102369Associated cell lines:
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Dai Q, Di W, Zhang Y, Gu S, Zhao J, Zhang B, Wang Y
Generation of a human induced pluripotent stem cell line (SIAISi010-A) from a 31-year-old healthy donor with Chinese Han genetic background
Dai Q et al. Generation of a human induced pluripotent stem cell line (SIAISi010-A) from a 31-year-old healthy donor with Chinese Han genetic background. . 2021-05-00. Pubmed ID: 33799282; DOI: 10.1016/j.scr.2021.102314 SIAISi010-A 2021-05-00 2021-05-00 PubMed: 33799282 DOI: 10.1016/j.scr.2021.102314Associated cell lines:
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Kato H, Maezawa Y, Ouchi Y, Takayama N, Sone M, Sone K, Takada-Watanabe A, Tsujimura K, Koshizaka M, Nagasawa S, Saitoh H, Ohtaka M, Nakanishi M, Tahara H, Shimamoto A, Iwama A, Eto K, Yokote K
Generation of disease-specific and CRISPR/Cas9-mediated gene-corrected iPS cells from a patient with adult progeria Werner syndrome
Kato H et al. Generation of disease-specific and CRISPR/Cas9-mediated gene-corrected iPS cells from a patient with adult progeria Werner syndrome. . 2021-05-00. Pubmed ID: 34087989; DOI: 10.1016/j.scr.2021.102360 CUi001-ACUi001-A-1 2021-05-00 2021-05-00 PubMed: 34087989 DOI: 10.1016/j.scr.2021.102360Associated cell lines:
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Wang J, Liu X, Du X, Ma Z, Liu B, Guo R, Feng B, Ma J, Cui H
Induced pluripotent stem cells derived from one 70-years-old male donor with the APOE-ε4/ε4 alleles
Wang J et al. Induced pluripotent stem cells derived from one 70-years-old male donor with the APOE-ε4/ε4 alleles. . 2021-05-00. Pubmed ID: 34088020; DOI: 10.1016/j.scr.2021.102395 HEBHMUi001-AHEBHMUi008-A 2021-05-00 2021-05-00 PubMed: 34088020 DOI: 10.1016/j.scr.2021.102395Associated cell lines:
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Calado SM, Bento D, Justino D, Mendes-Silva L, Marques N, Bragança J
Generation of a human induced pluripotent stem cell line (UALGi001-A) from a patient with Left-Ventricular Noncompaction Cardiomyopathy
Calado SM et al. Generation of a human induced pluripotent stem cell line (UALGi001-A) from a patient with Left-Ventricular Noncompaction Cardiomyopathy. . 2021-05-00. Pubmed ID: 33799278; DOI: 10.1016/j.scr.2021.102302 UALGi001-A 2021-05-00 2021-05-00 PubMed: 33799278 DOI: 10.1016/j.scr.2021.102302Associated cell lines:
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Du M, Li L, Hu Y, Mi H, Wang T
Derivation of a human induced pluripotent stem cell (hiPSC) line (PUMCSMi001-A) from peripheral blood mononuclear cells of one healthy female donor
Du M et al. Derivation of a human induced pluripotent stem cell (hiPSC) line (PUMCSMi001-A) from peripheral blood mononuclear cells of one healthy female donor. . 2021-05-00. Pubmed ID: 33812336; DOI: 10.1016/j.scr.2021.102312 PUMCSMi001-A 2021-05-00 2021-05-00 PubMed: 33812336 DOI: 10.1016/j.scr.2021.102312Associated cell lines:
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Si N, Zhang Z, Meng X, Huang X, Wang C, Pan B
Generation of an induced pluripotent stem cell line from a congenital microtia patient with 4p16.1 microduplication involving the long-range enhancer of HMX1
Si N et al. Generation of an induced pluripotent stem cell line from a congenital microtia patient with 4p16.1 microduplication involving the long-range enhancer of HMX1. . 2021-05-00. Pubmed ID: 34087987; DOI: 10.1016/j.scr.2021.102357 PSHi001-A 2021-05-00 2021-05-00 PubMed: 34087987 DOI: 10.1016/j.scr.2021.102357Associated cell lines:
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Yin X, Zhao D, Tian Z, Chen J, Chi J, Ke Y, He L, Zhang X, He Y, Feng Z
Generation of an induced pluripotent stem cell line from a patient with surfactant metabolism dysfunction carrying ABCA3 mutations
Yin X et al. Generation of an induced pluripotent stem cell line from a patient with surfactant metabolism dysfunction carrying ABCA3 mutations. . 2021-05-00. Pubmed ID: 33839547; DOI: 10.1016/j.scr.2021.102286 SMCPGHi001-A 2021-05-00 2021-05-00 PubMed: 33839547 DOI: 10.1016/j.scr.2021.102286Associated cell lines:
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Wu S, Zhu T, Sun Z, Wei X, Han X, Zou X, Sui R
Generation of a human induced pluripotent stem cell line from a Bietti crystalline corneoretinal dystrophy patient with CYP4V2 mutations
Wu S et al. Generation of a human induced pluripotent stem cell line from a Bietti crystalline corneoretinal dystrophy patient with CYP4V2 mutations. . 2021-05-00. Pubmed ID: 33857831; DOI: 10.1016/j.scr.2021.102330 PUMCHi014-A 2021-05-00 2021-05-00 PubMed: 33857831 DOI: 10.1016/j.scr.2021.102330Associated cell lines:
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Isaja L, Rodríguez-Varela MS, Marazita M, Mucci S, Itzcovich T, Chrem-Méndez P, Niikado M, Ferriol-Laffouillere SL, Allegri R, Martinetto H, Sevlever GE, Scassa ME, Surace EI, Romorini L
Generation of a human induced pluripotent stem cell line from a familial Alzheimer's disease PSEN1 T119I patient
Isaja L et al. Generation of a human induced pluripotent stem cell line from a familial Alzheimer's disease PSEN1 T119I patient. . 2021-05-00. Pubmed ID: 33839546; DOI: 10.1016/j.scr.2021.102325 FLENIi001-A 2021-05-00 2021-05-00 PubMed: 33839546 DOI: 10.1016/j.scr.2021.102325Associated cell lines:
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Ma L, Wu Z, Tang Q, Ji X, Mei Y, Peng T, Xu Q, Zhou W, Xiong M
Generation of an induced pluripotent stem cell line from a patient with global development delay carrying DYRK1A mutation (c.1730T>A) and a gene correction isogenic iPSC line
Ma L et al. Generation of an induced pluripotent stem cell line from a patient with global development delay carrying DYRK1A mutation (c.1730T>A) and a gene correction isogenic iPSC line. . 2021-05-00. Pubmed ID: 33813175; DOI: 10.1016/j.scr.2021.102305 FDCHi005-AFDCHi005-B 2021-05-00 2021-05-00 PubMed: 33813175 DOI: 10.1016/j.scr.2021.102305Associated cell lines:
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D'Anzi A, Altieri F, Perciballi E, Ferrari D, Torres B, Bernardini L, Lattante S, Sabatelli M, Vescovi AL, Rosati J
Generation of an induced pluripotent stem cell line (CSS012-A (7672)) carrying the p.G376D heterozygous mutation in the TARDBP protein
D'Anzi A et al. Generation of an induced pluripotent stem cell line (CSS012-A (7672)) carrying the p.G376D heterozygous mutation in the TARDBP protein. . 2021-05-00. Pubmed ID: 34087986; DOI: 10.1016/j.scr.2021.102356 CSSi012-A 2021-05-00 2021-05-00 PubMed: 34087986 DOI: 10.1016/j.scr.2021.102356Associated cell lines:
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Feng H, Li Q, Margolis RL, Li PP
Generation of a human induced pluripotent stem cell line JHUi003-A with homozygous mutation for spinocerebellar ataxia type 12 using genome editing
Feng H et al. Generation of a human induced pluripotent stem cell line JHUi003-A with homozygous mutation for spinocerebellar ataxia type 12 using genome editing. . 2021-05-00. Pubmed ID: 34087983; DOI: 10.1016/j.scr.2021.102346 JHUi003-A 2021-05-00 2021-05-00 PubMed: 34087983 DOI: 10.1016/j.scr.2021.102346Associated cell lines:
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Jung J, Hwang S, Seol H, Kim AH, Lee HM, Sung JJ, Jeong SM, Choi YM, Jun JK, Kim DW, Jang J
Generation of Brachyury-mCherry knock-in reporter human pluripotent stem cell line (SNUe003-A-2) using CRISPR/CAS9 nuclease
Jung J et al. Generation of Brachyury-mCherry knock-in reporter human pluripotent stem cell line (SNUe003-A-2) using CRISPR/CAS9 nuclease. . 2021-05-00. Pubmed ID: 33878708; DOI: 10.1016/j.scr.2021.102321 SNUe003-ASNUe003-A-2 2021-05-00 2021-05-00 PubMed: 33878708 DOI: 10.1016/j.scr.2021.102321Associated cell lines:
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Wu F, Chen Y, You K, Tan S, Xu Y, Wang PH, Liu S, Li YX
Generation of WAe001-A-58 human embryonic stem cell line with inducible expression of the SARS-CoV-2 nucleocapsid protein
Wu F et al. Generation of WAe001-A-58 human embryonic stem cell line with inducible expression of the SARS-CoV-2 nucleocapsid protein. . 2021-05-00. Pubmed ID: 33771478; DOI: 10.1016/j.scr.2021.102197; PMC: PMC7835078 WAe001-AWAe001-A-58 2021-05-00 2021-05-00 PubMed: 33771478 DOI: 10.1016/j.scr.2021.102197Associated cell lines:
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van Helden RWJ, Birket MJ, Freund C, Arendzen CH, Mikkers HM, Orlova V, de Coo RI, Mummery CL, Bellin M
Generation of three human induced pluripotent stem cell lines, LUMCi024-A, LUMCi025-A, and LUMCi026-A, from two patients with combined oxidative phosphorylation deficiency 8 and a related control
van Helden RWJ et al. Generation of three human induced pluripotent stem cell lines, LUMCi024-A, LUMCi025-A, and LUMCi026-A, from two patients with combined oxidative phosphorylation deficiency 8 and a related control. . 2021-05-00. Pubmed ID: 34088003; DOI: 10.1016/j.scr.2021.102374 LUMCi024-ALUMCi025-ALUMCi026-A 2021-05-00 2021-05-00 PubMed: 34088003 DOI: 10.1016/j.scr.2021.102374Associated cell lines:
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Rebs S, Beier J, Argyriou L, Schill T, Hasenfuss G, Vollmann D, Sossalla S, Streckfuss-Bömeke K
Generation and cardiac differentiation of an induced pluripotent stem cell line from a patient with arrhythmia-induced cardiomyopathy
Rebs S et al. Generation and cardiac differentiation of an induced pluripotent stem cell line from a patient with arrhythmia-induced cardiomyopathy. . 2021-05-00. Pubmed ID: 33631417; DOI: 10.1016/j.scr.2021.102263 UMGi157-A 2021-05-00 2021-05-00 PubMed: 33631417 DOI: 10.1016/j.scr.2021.102263Associated cell lines:
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Ge W, Song Y, Chu M, Liu Y, Yang B, Wang K, Yu B, Song C, Wang Y, Yang J
Generation of a human iPSC line CIBi009-A from a patient with familial hypercholesterolemia carrying variants of LDLR c.T1241G and APOB c.G1618T
Ge W et al. Generation of a human iPSC line CIBi009-A from a patient with familial hypercholesterolemia carrying variants of LDLR c.T1241G and APOB c.G1618T. . 2021-05-00. Pubmed ID: 33892292; DOI: 10.1016/j.scr.2021.102347 CIBi009-A 2021-05-00 2021-05-00 PubMed: 33892292 DOI: 10.1016/j.scr.2021.102347Associated cell lines:
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Wang D, Lin J, Jin M, Wang N
Establishment of a human iPSC line XMDYYYi001-A from a patient with Becker muscular dystrophy harboring duplications of exons 2-19 in dystrophin gene
Wang D et al. Establishment of a human iPSC line XMDYYYi001-A from a patient with Becker muscular dystrophy harboring duplications of exons 2-19 in dystrophin gene. . 2021-05-00. Pubmed ID: 33799273; DOI: 10.1016/j.scr.2021.102298 XMDYYYi001-A 2021-05-00 2021-05-00 PubMed: 33799273 DOI: 10.1016/j.scr.2021.102298Associated cell lines:
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Guo X, Qian R, Yang L, Chen H, Ding Y, Shan X, Chen C, Ni W, Lin J, Chu M
Establishment of an induced pluripotent stem cell line from a Noonan syndrome patient with the heterozygote mutation p.S257L (c.770C > T) in RAF1 gene
Guo X et al. Establishment of an induced pluripotent stem cell line from a Noonan syndrome patient with the heterozygote mutation p.S257L (c.770C > T) in RAF1 gene. . 2021-05-00. Pubmed ID: 33901818; DOI: 10.1016/j.scr.2021.102281 WMUi022-A 2021-05-00 2021-05-00 PubMed: 33901818 DOI: 10.1016/j.scr.2021.102281Associated cell lines:
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Wen J, He C, Feng Y, Song J, Liu J, Liu X, Mei L, Ling J, Chen H, Liu Y
Establishment of an iPSC line (CSUXHi004-A) from a patient with Waardenburg syndrome type I caused by a PAX3 splice mutation
Wen J et al. Establishment of an iPSC line (CSUXHi004-A) from a patient with Waardenburg syndrome type I caused by a PAX3 splice mutation. . 2021-05-00. Pubmed ID: 33774334; DOI: 10.1016/j.scr.2021.102300 CSUXHi004-A 2021-05-00 2021-05-00 PubMed: 33774334 DOI: 10.1016/j.scr.2021.102300Associated cell lines:
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Wu H, Yang B, Lv Z, Liu L, Gong W, Zhang S
Generation and characterization of human induced pluripotent stem cells line JLUEYEi001-A from a 45 year old female with Stickler syndrome
Wu H et al. Generation and characterization of human induced pluripotent stem cells line JLUEYEi001-A from a 45 year old female with Stickler syndrome. . 2021-05-00. Pubmed ID: 33647874; DOI: 10.1016/j.scr.2021.102255 JLUEYEi001-A 2021-05-00 2021-05-00 PubMed: 33647874 DOI: 10.1016/j.scr.2021.102255Associated cell lines:
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Chen PF, Chen T, Forman TE, Swanson AC, O'Kelly B, Dwyer SA, Buttermore ED, Kleiman R, Js Carrington S, Lavery DJ, Swanson LC, Olson HE, Sahin M
Generation and characterization of human induced pluripotent stem cells (iPSCs) from three male and three female patients with CDKL5 Deficiency Disorder (CDD)
Chen PF et al. Generation and characterization of human induced pluripotent stem cells (iPSCs) from three male and three female patients with CDKL5 Deficiency Disorder (CDD). . 2021-05-00. Pubmed ID: 33714067; DOI: 10.1016/j.scr.2021.102276; PMC: PMC8953930 BCHi001-ABCHi001-BBCHi002-ABCHi002-BBCHi003-ABCHi003-BBCHi004-ABCHi004-BBCHi005-ABCHi005-BBCHi006-ABCHi006-B 2021-05-00 2021-05-00 PubMed: 33714067 DOI: 10.1016/j.scr.2021.102276 -
Wang Y, Sun H, Wang Z, Zhang Q, Yang J, Liu Y, Liu H, Shi C, Wang Y, Xu Y
Generation of induced pluripotent stem cell line (ZZUi019-A) derived from skin fibroblasts from a healthy volunteer
Wang Y et al. Generation of induced pluripotent stem cell line (ZZUi019-A) derived from skin fibroblasts from a healthy volunteer. . 2021-05-00. Pubmed ID: 33740644; DOI: 10.1016/j.scr.2021.102285 ZZUi005-AZZUi019-A 2021-05-00 2021-05-00 PubMed: 33740644 DOI: 10.1016/j.scr.2021.102285 -
Begentas OC, Koc D, Yurtogullari S, Temel M, Akcali KC, Demirkaya S, Kiris E
Generation and characterization of human induced pluripotent stem cell line METUi001-A from a 25-year-old male patient with relapsing-remitting multiple sclerosis
Begentas OC et al. Generation and characterization of human induced pluripotent stem cell line METUi001-A from a 25-year-old male patient with relapsing-remitting multiple sclerosis. . 2021-05-00. Pubmed ID: 34087999; DOI: 10.1016/j.scr.2021.102370 METUi001-A 2021-05-00 2021-05-00 PubMed: 34087999 DOI: 10.1016/j.scr.2021.102370Associated cell lines:
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Li W, Henze S, Luo X, Ulbricht Y, Richter A, Di Donato N, Wilde AAM, Guan K
Generation of iPSC lines from CPVT patient carrying heterozygous mutation p.A2254V in the ryanodine receptor 2 gene
Li W et al. Generation of iPSC lines from CPVT patient carrying heterozygous mutation p.A2254V in the ryanodine receptor 2 gene. . 2021-05-00. Pubmed ID: 33640691; DOI: 10.1016/j.scr.2021.102259 UMGi041-B 2021-05-00 2021-05-00 PubMed: 33640691 DOI: 10.1016/j.scr.2021.102259Associated cell lines:
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Liu M, Li X, Fu W, Wang M, Liu Y, Wang L, Hu L, Zhao X, Dong J
Induced pluripotent stem cell (iPSC) line (ZZUNEUi009-A) from a healthy female individual
Liu M et al. Induced pluripotent stem cell (iPSC) line (ZZUNEUi009-A) from a healthy female individual. . 2021-05-00. Pubmed ID: 33730648; DOI: 10.1016/j.scr.2021.102275 ZZUNEUi009-A 2021-05-00 2021-05-00 PubMed: 33730648 DOI: 10.1016/j.scr.2021.102275Associated cell lines:
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Xu X, Dong L, Ma C, Xu X, Wu H, Wang J, Zhou P, Cao Y, Wei Z
Establishment of an induced pluripotent stem cell line from a patient with primary ciliary dyskinesia carrying biallelic mutations in CCNO
Xu X et al. Establishment of an induced pluripotent stem cell line from a patient with primary ciliary dyskinesia carrying biallelic mutations in CCNO. . 2021-05-00. Pubmed ID: 34088001; DOI: 10.1016/j.scr.2021.102372 AMUFAHi001-A 2021-05-00 2021-05-00 PubMed: 34088001 DOI: 10.1016/j.scr.2021.102372Associated cell lines:
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Wei C, Luo Q, Wang B, Long Y, Zhang M, Shan W, Yu X, Xu Y, Qian P, Huang H
Generation of a FTO gene knockout human embryonic stem cell line using CRISPR/Cas9 editing
Wei C et al. Generation of a FTO gene knockout human embryonic stem cell line using CRISPR/Cas9 editing. . 2021-05-00. Pubmed ID: 34087991; DOI: 10.1016/j.scr.2021.102362 WAe001-A-72 2021-05-00 2021-05-00 PubMed: 34087991 DOI: 10.1016/j.scr.2021.102362Associated cell lines:
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Gao X, Qiu SW, Wang WQ, Kang DY, Su N, Dai P, Yuan YY
Generation of a gene corrected human isogenic iPSC line (CPGHi002-A-1) from a DDOD patient with heterozygous c.1516 C>T mutation in the ATP6V1B2 gene
Gao X et al. Generation of a gene corrected human isogenic iPSC line (CPGHi002-A-1) from a DDOD patient with heterozygous c.1516 C>T mutation in the ATP6V1B2 gene. . 2021-05-00. Pubmed ID: 33714068; DOI: 10.1016/j.scr.2021.102271 CPGHi002-ACPGHi002-A-1 2021-05-00 2021-05-00 PubMed: 33714068 DOI: 10.1016/j.scr.2021.102271Associated cell lines:
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Fang J, Wang Y, Wang Z, Sun H, Zhang Q, Yang J, Liu Y, Liu H, Shi C, Xu Y, Zhang X, Kan Q
Generation of induced pluripotent stem cell line (ZZUi0026-A) from a patient with spinocerebellar ataxia type 3
Fang J et al. Generation of induced pluripotent stem cell line (ZZUi0026-A) from a patient with spinocerebellar ataxia type 3. . 2021-05-00. Pubmed ID: 34087977; DOI: 10.1016/j.scr.2021.102205 ZZUi026-A 2021-05-00 2021-05-00 PubMed: 34087977 DOI: 10.1016/j.scr.2021.102205Associated cell lines:
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Zhao H, Wang L, Wu J, Ren J, Chen Q, Luo H, Zuo X, Tang Y
Establishment of an induced pluripotent stem cell line (CSUi003-A) from fibroblasts of a healthy elderly individual
Zhao H et al. Establishment of an induced pluripotent stem cell line (CSUi003-A) from fibroblasts of a healthy elderly individual. . 2021-05-00. Pubmed ID: 33845242; DOI: 10.1016/j.scr.2021.102326 CSUi003-A 2021-05-00 2021-05-00 PubMed: 33845242 DOI: 10.1016/j.scr.2021.102326Associated cell lines:
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Hernández D, Morgan Schlicht S, Daniszewski M, Karch CM, Dominantly Inherited Alzheimer Network (DIAN), Goate AM, Pébay A
Generation of a gene-corrected human isogenic iPSC line from an Alzheimer's disease iPSC line carrying the London mutation in APP (V717I)
Hernández D et al. Generation of a gene-corrected human isogenic iPSC line from an Alzheimer's disease iPSC line carrying the London mutation in APP (V717I). . 2021-05-00. Pubmed ID: 34088002; DOI: 10.1016/j.scr.2021.102373; PMC: PMC10084742 UOMELBi002-A 2021-05-00 2021-05-00 PubMed: 34088002 DOI: 10.1016/j.scr.2021.102373Associated cell lines:
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Srivastava A, Alagarsamy KN, Sequiera GL, Rockman-Greenberg C, Dhingra S
Human induced pluripotent stem cell (hiPSC) line UOMi006-A derived from PBMCs of a patient with Kearns-Sayre syndrome
Srivastava A et al. Human induced pluripotent stem cell (hiPSC) line UOMi006-A derived from PBMCs of a patient with Kearns-Sayre syndrome. . 2021-05-00. Pubmed ID: 33901817; DOI: 10.1016/j.scr.2021.102355 UOMi002-AUOMi005-AUOMi006-A 2021-05-00 2021-05-00 PubMed: 33901817 DOI: 10.1016/j.scr.2021.102355 -
Song X, Feng J, Lan X, Tang X, Xu W, Shen J, Yu G, Jia J, Zhang H, Lu Q, Wu S
Generation and characterization of an iPSC line (SHCMDLi001-A) from a 12-year-old Chinese Han patient with TRAF7 syndrome and of an iPSC line (SHCMDLi002-A) from a control individual
Song X et al. Generation and characterization of an iPSC line (SHCMDLi001-A) from a 12-year-old Chinese Han patient with TRAF7 syndrome and of an iPSC line (SHCMDLi002-A) from a control individual. . 2021-05-00. Pubmed ID: 34088006; DOI: 10.1016/j.scr.2021.102377 SHCMDLi001-ASHCMDLi002-A 2021-05-00 2021-05-00 PubMed: 34088006 DOI: 10.1016/j.scr.2021.102377Associated cell lines:
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Maneepitasut W, Wongkummool W, Tong-Ngam P, Promthep K, Tubsuwan A, Khine Linn A, Phakdeekitcharoen B, Borwornpinyo S, Kitiyanant N, Phanthong P, Hongeng S
Generation of human induced pluripotent stem cell line (MUi026-A) from a patient with autosomal dominant polycystic kidney disease carrying PKD1 point mutation
Maneepitasut W et al. Generation of human induced pluripotent stem cell line (MUi026-A) from a patient with autosomal dominant polycystic kidney disease carrying PKD1 point mutation. . 2021-05-00. Pubmed ID: 33799277; DOI: 10.1016/j.scr.2021.102306 MUi026-A 2021-05-00 2021-05-00 PubMed: 33799277 DOI: 10.1016/j.scr.2021.102306Associated cell lines:
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Tran TT, Nguyen TH, Nguyen TT, Nguyen XH
Establishment of a Vietnamese ethnicity induced pluripotent stem cell line (VRISGi001-A) from umbilical cord blood hematopoietic stem cells under a feeder-free system
Tran TT et al. Establishment of a Vietnamese ethnicity induced pluripotent stem cell line (VRISGi001-A) from umbilical cord blood hematopoietic stem cells under a feeder-free system. . 2021-05-00. Pubmed ID: 33878709; DOI: 10.1016/j.scr.2021.102345 VRISGi001-A 2021-05-00 2021-05-00 PubMed: 33878709 DOI: 10.1016/j.scr.2021.102345Associated cell lines:
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Wang Z, Sun H, Zhang Q, Yang J, Liu Y, Liu H, Shi C, Wang Y, Xu Y
Generation of induced pluripotent stem cell line (ZZUi0024-A) from a 51-year-old patient with APP gene mutation in Alzheimer' s disease
Wang Z et al. Generation of induced pluripotent stem cell line (ZZUi0024-A) from a 51-year-old patient with APP gene mutation in Alzheimer' s disease. . 2021-05-00. Pubmed ID: 33652304; DOI: 10.1016/j.scr.2021.102267 ZZUi024-A 2021-05-00 2021-05-00 PubMed: 33652304 DOI: 10.1016/j.scr.2021.102267Associated cell lines:
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Li Z, Zhang X, Li X, Yang Y, Xin H, Yang X, Liu N, Gai Z, Liu Y
A non-integrated iPSC line (SDQLCHi042-A) from a boy suffering from familial combined hyperlipidemia with compound heterozygous mutations of lipoprotein lipase gene
Li Z et al. A non-integrated iPSC line (SDQLCHi042-A) from a boy suffering from familial combined hyperlipidemia with compound heterozygous mutations of lipoprotein lipase gene. . 2021-05-00. Pubmed ID: 34087978; DOI: 10.1016/j.scr.2021.102313 SDQLCHi042-A 2021-05-00 2021-05-00 PubMed: 34087978 DOI: 10.1016/j.scr.2021.102313Associated cell lines:
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Argenziano MA, Burgos Angulo M, Najari Beidokhti M, Yang J, Bertalovitz AC, McDonald TV
Generation of a heterozygous FLNC mutation-carrying human iPSC line, USFi002-A, for modeling dilated cardiomyopathy
Argenziano MA et al. Generation of a heterozygous FLNC mutation-carrying human iPSC line, USFi002-A, for modeling dilated cardiomyopathy. . 2021-05-00. Pubmed ID: 34088019; DOI: 10.1016/j.scr.2021.102394 USFi002-A 2021-05-00 2021-05-00 PubMed: 34088019 DOI: 10.1016/j.scr.2021.102394Associated cell lines:
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Liu F, Fan Y, Fan L, Li M, Zhang Q, Mao C, Wu J, Zhang S, Hu Z, Shi C, Xu Y
Generation of induced pluripotent stem cell line (ZZUi0021-A) from a patient with spinocerebellar ataxia type 19
Liu F et al. Generation of induced pluripotent stem cell line (ZZUi0021-A) from a patient with spinocerebellar ataxia type 19. . 2021-05-00. Pubmed ID: 34087979; DOI: 10.1016/j.scr.2021.102320 ZZUi021-A 2021-05-00 2021-05-00 PubMed: 34087979 DOI: 10.1016/j.scr.2021.102320Associated cell lines:
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Gerace D, Boulanger KR, Hyoje-Ryu Kenty J, Melton DA
Generation of a heterozygous GAPDH-Luciferase human ESC line (HVRDe008-A-1) for in vivo monitoring of stem cells and their differentiated progeny
Gerace D et al. Generation of a heterozygous GAPDH-Luciferase human ESC line (HVRDe008-A-1) for in vivo monitoring of stem cells and their differentiated progeny. . 2021-05-00. Pubmed ID: 34088000; DOI: 10.1016/j.scr.2021.102371 HVRDe008-AHVRDe008-A-1 2021-05-00 2021-05-00 PubMed: 34088000 DOI: 10.1016/j.scr.2021.102371Associated cell lines:
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Srivastava A, Lester Sequiera G, Narayan Alagarsamy K, Rockman-Greenberg C, Dhingra S
Generation of human induced pluripotent stem cell (hiPSC) line UOMi005-A from PBMCs of a patient with Kearns-Sayre syndrome
Srivastava A et al. Generation of human induced pluripotent stem cell (hiPSC) line UOMi005-A from PBMCs of a patient with Kearns-Sayre syndrome. . 2021-05-00. Pubmed ID: 33756177; DOI: 10.1016/j.scr.2021.102283 UOMi005-A 2021-05-00 2021-05-00 PubMed: 33756177 DOI: 10.1016/j.scr.2021.102283Associated cell lines:
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Zhang Y, Zhu Y, Lin Y, Liu H, Chen H, Ju W, Cui C, Chen M
Establishment of an iPSC line (JSPHi001-A) from a patient with familial dilated cardiomyopathy and atrial fibrillation caused by LMNA missense mutation (c.1003C > T)
Zhang Y et al. Establishment of an iPSC line (JSPHi001-A) from a patient with familial dilated cardiomyopathy and atrial fibrillation caused by LMNA missense mutation (c.1003C > T). . 2021-05-00. Pubmed ID: 33887581; DOI: 10.1016/j.scr.2021.102349 JSPHi001-A 2021-05-00 2021-05-00 PubMed: 33887581 DOI: 10.1016/j.scr.2021.102349Associated cell lines:
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Zhang L, Ren Q, Liu X, Liu G, Meng S, Xiahou K, Zhang Y, Jiang N, Zhou W
Generation of induced pluripotent stem cell line (IPTi002-A) from an 87-year old sporadic Alzheimer's disease patient with APOE3 (ε3/ε3) genotype
Zhang L et al. Generation of induced pluripotent stem cell line (IPTi002-A) from an 87-year old sporadic Alzheimer's disease patient with APOE3 (ε3/ε3) genotype. . 2021-05-00. Pubmed ID: 33799279; DOI: 10.1016/j.scr.2021.102282 IPTi001-AIPTi002-A 2021-05-00 2021-05-00 PubMed: 33799279 DOI: 10.1016/j.scr.2021.102282 -
Wang Y, Wang Z, Sun H, Zhang Q, Yang J, Liu Y, Liu H, Shi C, Zhang R, Xu Y
Generation of induced pluripotent stem cell line (ZZUi028-A) from a 52-year-old Chinese Han healthy female individual
Wang Y et al. Generation of induced pluripotent stem cell line (ZZUi028-A) from a 52-year-old Chinese Han healthy female individual. . 2021-05-00. Pubmed ID: 34088010; DOI: 10.1016/j.scr.2021.102381 ZZUi011-AZZUi028-A 2021-05-00 2021-05-00 PubMed: 34088010 DOI: 10.1016/j.scr.2021.102381 -
Li Y, Li J, Zhou T, Pan G, Huang K
Generation of PARP1 gene knockout human embryonic stem cell line using CRISPR/Cas9
Li Y et al. Generation of PARP1 gene knockout human embryonic stem cell line using CRISPR/Cas9. . 2021-05-00. Pubmed ID: 33740642; DOI: 10.1016/j.scr.2021.102288 WAe001-A-63 2021-05-00 2021-05-00 PubMed: 33740642 DOI: 10.1016/j.scr.2021.102288Associated cell lines:
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Ben-Zvi H, Korover N, Rabinski T, Ofir R, Cohen S
Generation and characterization of three human induced pluripotent stem cell lines (iPSC) from two family members with dilated cardiomyopathy and left ventricular noncompaction (DCM-LVNC) and one healthy heterozygote sibling
Ben-Zvi H et al. Generation and characterization of three human induced pluripotent stem cell lines (iPSC) from two family members with dilated cardiomyopathy and left ventricular noncompaction (DCM-LVNC) and one healthy heterozygote sibling. . 2021-05-00. Pubmed ID: 34088011; DOI: 10.1016/j.scr.2021.102382 BGUi008-ABGUi009-ABGUi010-A 2021-05-00 2021-05-00 PubMed: 34088011 DOI: 10.1016/j.scr.2021.102382 -
Yuan F, Wang S, Wang Y, Wang A, Wang C, Luo X, Xu Q, Yin R, Cheng H, Wang C, Guo M, Zhang Y, Xi J, Yang J, Sun X, Yan J, Zeng F, Chen Y
Generation and characterization of the induced pluripotent stem cell line SHCDNi004-A from a ten-year-old Chinese boy with X-linked mental retardation in IL1RAPL1 deficiency
Yuan F et al. Generation and characterization of the induced pluripotent stem cell line SHCDNi004-A from a ten-year-old Chinese boy with X-linked mental retardation in IL1RAPL1 deficiency. . 2021-05-00. Pubmed ID: 33774333; DOI: 10.1016/j.scr.2021.102292 SHCDNi004-A 2021-05-00 2021-05-00 PubMed: 33774333 DOI: 10.1016/j.scr.2021.102292Associated cell lines:
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Shang S, Chen K, Cai G, Bai X, Chen X, Li Q
Establishment of PLAFMCi004-A induced pluripotent stem cells derived from PBMCs from a healthy individual
Shang S et al. Establishment of PLAFMCi004-A induced pluripotent stem cells derived from PBMCs from a healthy individual. . 2021-05-00. Pubmed ID: 33878710; DOI: 10.1016/j.scr.2021.102316 ZZUSAHi002-A 2021-05-00 2021-05-00 PubMed: 33878710 DOI: 10.1016/j.scr.2021.102316Associated cell lines:
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Zhou Y, Wang J, Li H, Li A, Wang G, Tan X, Lei M, Zhang Y
Establishment of iPSC line from a Chinese infant (XACHi012-A) with Jervell and Lange-Nielsen syndrome carrying combined KCNQ1 frameshift c.431delC(p.I145Sfs*92) and nonsense c.1175G > A (p.W392X) variants and two iPSC lines from the parents (XACHi013-A, XACHi014-A)
Zhou Y et al. Establishment of iPSC line from a Chinese infant (XACHi012-A) with Jervell and Lange-Nielsen syndrome carrying combined KCNQ1 frameshift c.431delC(p.I145Sfs*92) and nonsense c.1175G > A (p.W392X) variants and two iPSC lines from the parents (XACHi013-A, XACHi014-A). . 2021-05-00. Pubmed ID: 34088017; DOI: 10.1016/j.scr.2021.102391 XACHi012-AXACHi013-AXACHi014-A 2021-05-00 2021-05-00 PubMed: 34088017 DOI: 10.1016/j.scr.2021.102391Associated cell lines:
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Wu J, Ren J, Luo H, Zuo X, Tang Y
Generation of patient-specific induced pluripotent stem cell line (CSUi002-A) from a patient with isolated dystonia carrying TOR1A mutation
Wu J et al. Generation of patient-specific induced pluripotent stem cell line (CSUi002-A) from a patient with isolated dystonia carrying TOR1A mutation. . 2021-05-00. Pubmed ID: 33706202; DOI: 10.1016/j.scr.2021.102277 CSUi002-A 2021-05-00 2021-05-00 PubMed: 33706202 DOI: 10.1016/j.scr.2021.102277Associated cell lines:
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Ge N, Liu M, Zhu X, Krawczyk J, McInerney V, Shen S, O'Brien T, Prendiville T
Generation and characterization of three induced pluripotent stem cell lines (NUIGi047-A, NUIGi047-B, NUIGi047-C) from a 7-year-old healthy Caucasian male
Ge N et al. Generation and characterization of three induced pluripotent stem cell lines (NUIGi047-A, NUIGi047-B, NUIGi047-C) from a 7-year-old healthy Caucasian male. . 2021-05-00. Pubmed ID: 34088016; DOI: 10.1016/j.scr.2021.102389 NUIGi047-ANUIGi047-BNUIGi047-C 2021-05-00 2021-05-00 PubMed: 34088016 DOI: 10.1016/j.scr.2021.102389Associated cell lines:
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Eberhardt K, Jumo H, D'Amore A, Alecu JE, Ziegler M, Afshar Saber W, Sahin M, Ebrahimi-Fakhari D
Generation and characterization of six human induced pluripotent stem cell lines (iPSC) from three families with AP4M1-associated hereditary spastic paraplegia (SPG50)
Eberhardt K et al. Generation and characterization of six human induced pluripotent stem cell lines (iPSC) from three families with AP4M1-associated hereditary spastic paraplegia (SPG50). . 2021-05-00. Pubmed ID: 34087981; DOI: 10.1016/j.scr.2021.102335; PMC: PMC8824776 BCHNEUi007-ABCHNEUi008-ABCHNEUi009-ABCHNEUi010-ABCHNEUi011-ABCHNEUi012-A 2021-05-00 2021-05-00 PubMed: 34087981 DOI: 10.1016/j.scr.2021.102335Associated cell lines:
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Yada Y, Kondo T, Suga M, Tsukita K, Enami T, Shibukawa R, Sagara Y, Okanishi Y, Imamura K, Kihara T, Inoue H
Human induced pluripotent stem cells generated from a patient with idiopathic basal ganglia calcification
Yada Y et al. Human induced pluripotent stem cells generated from a patient with idiopathic basal ganglia calcification. . 2021-05-00. Pubmed ID: 33714066; DOI: 10.1016/j.scr.2021.102274 BRCi007-A 2021-05-00 2021-05-00 PubMed: 33714066 DOI: 10.1016/j.scr.2021.102274Associated cell lines:
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Tang X, Fu J, Chen Z, Luo L, Li DW, Liu Y
Generation of a homozygous CRISPR/Cas9-mediated knockout H9 hESC subline for the MERTK locus
Tang X et al. Generation of a homozygous CRISPR/Cas9-mediated knockout H9 hESC subline for the MERTK locus. . 2021-05-00. Pubmed ID: 33812335; DOI: 10.1016/j.scr.2021.102310 WAe009-A-39 2021-05-00 2021-05-00 PubMed: 33812335 DOI: 10.1016/j.scr.2021.102310Associated cell lines:
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Song B, Cheng Y, Cao D, Liu N, Guan H, Du L, Zhang H, Liang Y, Xian J, Sun X
Generation of induced pluripotent stem cell line GZHMCi006-A from amniotic fluid-derived cells with deletion 14q syndrome
Song B et al. Generation of induced pluripotent stem cell line GZHMCi006-A from amniotic fluid-derived cells with deletion 14q syndrome. . 2021-05-00. Pubmed ID: 33894549; DOI: 10.1016/j.scr.2021.102315 GZHMCi006-A 2021-05-00 2021-05-00 PubMed: 33894549 DOI: 10.1016/j.scr.2021.102315Associated cell lines:
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Ma L, Prada AM, Schmidt M, Morrow EM
Generation of pathogenic TPP1 mutations in human stem cells as a model for neuronal ceroid lipofuscinosis type 2 disease
Ma L et al. Generation of pathogenic TPP1 mutations in human stem cells as a model for neuronal ceroid lipofuscinosis type 2 disease. . 2021-05-00. Pubmed ID: 33845243; DOI: 10.1016/j.scr.2021.102323; PMC: PMC9173593 WAe009-A-49WAe009-A-51WAe009-A-54WAe009-A-55 2021-05-00 2021-05-00 PubMed: 33845243 DOI: 10.1016/j.scr.2021.102323Associated cell lines:
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Grossmann L, Yde Ohki CM, Döring C, Hoffmann P, Herms S, Werling AM, Walitza S, Grünblatt E
Generation of integration-free induced pluripotent stem cell lines from four pediatric ADHD patients
Grossmann L et al. Generation of integration-free induced pluripotent stem cell lines from four pediatric ADHD patients. . 2021-05-00. Pubmed ID: 33662736; DOI: 10.1016/j.scr.2021.102268 TMPi006-ATMPi006-BTMPi007-ATMPi007-BTMPi008-ATMPi009-ATMPi009-B 2021-05-00 2021-05-00 PubMed: 33662736 DOI: 10.1016/j.scr.2021.102268 -
Rhoden A, Friedrich FW, Brandt T, Raabe J, Schweizer M, Meisterknecht J, Wittig I, Ulmer BM, Klampe B, Uebeler J, Piasecki A, Lorenz K, Eschenhagen T, Hansen A, Cuello F
Sulforaphane exposure impairs contractility and mitochondrial function in three-dimensional engineered heart tissue
Rhoden A et al. Sulforaphane exposure impairs contractility and mitochondrial function in three-dimensional engineered heart tissue. . 2021-05-00. Pubmed ID: 33831709; DOI: 10.1016/j.redox.2021.101951; PMC: PMC8056268 UKEi001-A 2021-05-00 2021-05-00 PubMed: 33831709 DOI: 10.1016/j.redox.2021.101951Associated cell lines:
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Kumar M, Wadhwa S, Tyagi N, Ahmad I, Kumar S, Sagar S, Zahra S, Kamai A, Shamim U, Kapoor S, Faruq M
Generation of induced pluripotent stem cell line (IGIBi007-A) from a patient with a novel acromesomelic dysplasia, PRKG2 type (AMDP)
Kumar M et al. Generation of induced pluripotent stem cell line (IGIBi007-A) from a patient with a novel acromesomelic dysplasia, PRKG2 type (AMDP). . 2021-05-00. Pubmed ID: 33887582; DOI: 10.1016/j.scr.2021.102340 IGIBi002-AIGIBi003-AIGIBi004-AIGIBi007-A 2021-05-00 2021-05-00 PubMed: 33887582 DOI: 10.1016/j.scr.2021.102340Associated cell lines:
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Yde Ohki CM, Grossmann L, Döring C, Hoffmann P, Herms S, Werling AM, Walitza S, Grünblatt E
Generation of integration-free induced pluripotent stem cells from healthy individuals
Yde Ohki CM et al. Generation of integration-free induced pluripotent stem cells from healthy individuals. . 2021-05-00. Pubmed ID: 33667761; DOI: 10.1016/j.scr.2021.102269 TMPi001-ATMPi001-BTMPi002-ATMPi002-BTMPi003-ATMPi003-BTMPi004-ATMPi004-BTMPi005-ATMPi005-B 2021-05-00 2021-05-00 PubMed: 33667761 DOI: 10.1016/j.scr.2021.102269 -
Silva TP, Pereira CA, Raposo AC, Oliveira AR, Arez M, Cabral JMS, Milagre I, Carmo-Fonseca M, Rocha STD
Generation and characterization of induced pluripotent stem cells heterozygous for the Portuguese BRCA2 founder mutation
Silva TP et al. Generation and characterization of induced pluripotent stem cells heterozygous for the Portuguese BRCA2 founder mutation. . 2021-05-00. Pubmed ID: 34087993; DOI: 10.1016/j.scr.2021.102364 IBBISTi003-AIBBISTi003-BIBBISTi003-C 2021-05-00 2021-05-00 PubMed: 34087993 DOI: 10.1016/j.scr.2021.102364Associated cell lines:
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Sarafian R, Morato-Marques M, Borsoi J, Tófoli-Araújo F, Pinheiro M, Medina-Armenteros Y, Lotufo PA, Bensenor IM, Pereira LV
Generation of 6 lines of human pluripotent stem cells from hypertensive patients and 3 lines of human pluripotent stem cell from normotensive patients
Sarafian R et al. Generation of 6 lines of human pluripotent stem cells from hypertensive patients and 3 lines of human pluripotent stem cell from normotensive patients. . 2021-05-00. Pubmed ID: 34088012; DOI: 10.1016/j.scr.2021.102384 LANCEi023-ALANCEi024-ALANCEi025-ALANCEi026-ALANCEi027-ALANCEi028-ALANCEi029-ALANCEi030-ALANCEi031-A 2021-05-00 2021-05-00 PubMed: 34088012 DOI: 10.1016/j.scr.2021.102384Associated cell lines:
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Yasui H, Nishinaga Y, Taki S, Takahashi K, Isobe Y, Shimizu M, Koike C, Taki T, Sakamoto A, Katsumi K, Ishii K, Sato K
Near-infrared photoimmunotherapy targeting GPR87: Development of a humanised anti-GPR87 mAb and therapeutic efficacy on a lung cancer mouse model
Yasui H et al. Near-infrared photoimmunotherapy targeting GPR87: Development of a humanised anti-GPR87 mAb and therapeutic efficacy on a lung cancer mouse model. . 2021-05-00. Pubmed ID: 33993055; DOI: 10.1016/j.ebiom.2021.103372; PMC: PMC8138482 KMUe003-A 2021-05-00 2021-05-00 PubMed: 33993055 DOI: 10.1016/j.ebiom.2021.103372Associated cell lines:
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Xiao X, Chen Y, Peng L, Zhang T
Generation of a homozygous ALX1 knockout human embryonic stem cell line (WAe001-A-060) by a CRISPR/Cas9 system
Xiao X et al. Generation of a homozygous ALX1 knockout human embryonic stem cell line (WAe001-A-060) by a CRISPR/Cas9 system. . 2021-05-00. Pubmed ID: 33799274; DOI: 10.1016/j.scr.2021.102309 WAe001-AWAe001-A-60 2021-05-00 2021-05-00 PubMed: 33799274 DOI: 10.1016/j.scr.2021.102309Associated cell lines:
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Yuzuriha A, Nakamura S, Sugimoto N, Kihara S, Nakagawa M, Yamamoto T, Sekiguchi K, Eto K
Extracellular laminin regulates hematopoietic potential of pluripotent stem cells through integrin β1-ILK-β-catenin-JUN axis
Yuzuriha A et al. Extracellular laminin regulates hematopoietic potential of pluripotent stem cells through integrin β1-ILK-β-catenin-JUN axis. . 2021-05-00. Pubmed ID: 33813173; DOI: 10.1016/j.scr.2021.102287 KUIMSe003-AKUIMSe004-A 2021-05-00 2021-05-00 PubMed: 33813173 DOI: 10.1016/j.scr.2021.102287Associated cell lines:
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Lucchino V, Scaramuzzino L, Scalise S, Grillone K, Lo Conte M, Esposito C, Aguglia U, Ferlazzo E, Perrotti N, Malatesta P, Parrotta EI, Cuda G
Generation of human induced pluripotent stem cell lines (UNIMGi003-A and UNIMGi004-A) from two Italian siblings affected by Unverricht-Lundborg disease
Lucchino V et al. Generation of human induced pluripotent stem cell lines (UNIMGi003-A and UNIMGi004-A) from two Italian siblings affected by Unverricht-Lundborg disease. . 2021-05-00. Pubmed ID: 33865103; DOI: 10.1016/j.scr.2021.102329 UNIMGi003-AUNIMGi004-A 2021-05-00 2021-05-00 PubMed: 33865103 DOI: 10.1016/j.scr.2021.102329Associated cell lines:
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Micheu MM, Rosca AM
Patient-specific induced pluripotent stem cells as "disease-in-a-dish" models for inherited cardiomyopathies and channelopathies - 15 years of research
Micheu MM et al. Patient-specific induced pluripotent stem cells as "disease-in-a-dish" models for inherited cardiomyopathies and channelopathies - 15 years of research. . 2021-04-26. Pubmed ID: 33959219; DOI: 10.4252/wjsc.v13.i4.281; PMC: PMC8080539 PSMi004-APSMi005-APSMi006-ANUIGi005-ANUIGi005-BNUIGi005-CNUIGi006-ANUIGi006-BNUIGi006-CNUIGi007-ANUIGi007-B 2021-04-26 2021-04-26 PubMed: 33959219 DOI: 10.4252/wjsc.v13.i4.281Associated cell lines:
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Sim CB, Phipson B, Ziemann M, Rafehi H, Mills RJ, Watt KI, Abu-Bonsrah KD, Kalathur RKR, Voges HK, Dinh DT, Ter Huurne M, Vivien CJ, Kaspi A, Kaipananickal H, Hidalgo A, Delbridge LMD, Robker RL, Gregorevic P, Dos Remedios CG, Lal S, Piers AT, Konstantinov IE, Elliott DA, El-Osta A, Oshlack A, Hudson JE, Porrello ER
Sex-Specific Control of Human Heart Maturation by the Progesterone Receptor
Sim CB et al. Sex-Specific Control of Human Heart Maturation by the Progesterone Receptor. . 2021-04-20. Pubmed ID: 33682422; DOI: 10.1161/circulationaha.120.051921; PMC: PMC8055196 MCRIi001-AMCRIi004-A 2021-04-20 2021-04-20 PubMed: 33682422 DOI: 10.1161/circulationaha.120.051921Associated cell lines:
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Toledo MAS, Gatz M, Sontag S, Gleixner KV, Eisenwort G, Feldberg K, Hamouda AEI, Kluge F, Guareschi R, Rossetti G, Sechi AS, Dufva OMJ, Mustjoki SM, Maurer A, Schüler HM, Goetzke R, Braunschweig T, Kaiser A, Panse J, Jawhar M, Reiter A, Hilberg F, Ettmayer P, Wagner W, Koschmieder S, Brümmendorf TH, Valent P, Chatain N, Zenke M
Nintedanib targets KIT D816V neoplastic cells derived from induced pluripotent stem cells of systemic mastocytosis
Toledo MAS et al. Nintedanib targets KIT D816V neoplastic cells derived from induced pluripotent stem cells of systemic mastocytosis. . 2021-04-15. Pubmed ID: 33512435; DOI: 10.1182/blood.2019004509 UKAi004-AUKAi004-BUKAi004-CUKAi004-DUKAi004-EUKAi007-AUKAi007-BUKAi008-AUKAi008-BUKAi008-CESIBIe003-A-8ESIBIe003-A-9 2021-04-15 2021-04-15 PubMed: 33512435 DOI: 10.1182/blood.2019004509 -
Alle Q, Le Borgne E, Milhavet O, Lemaitre JM
Reprogramming: Emerging Strategies to Rejuvenate Aging Cells and Tissues
Alle Q et al. Reprogramming: Emerging Strategies to Rejuvenate Aging Cells and Tissues. . 2021-04-13. Pubmed ID: 33924362; DOI: 10.3390/ijms22083990; PMC: PMC8070588 REGUi003-A 2021-04-13 2021-04-13 PubMed: 33924362 DOI: 10.3390/ijms22083990Associated cell lines:
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Liedtke M, Völkner C, Jürs AV, Peter F, Rabenstein M, Hermann A, Frech MJ
Pathophysiological In Vitro Profile of Neuronal Differentiated Cells Derived from Niemann-Pick Disease Type C2 Patient-Specific iPSCs Carrying the NPC2 Mutations c.58G>T/c.140G>T
Liedtke M et al. Pathophysiological In Vitro Profile of Neuronal Differentiated Cells Derived from Niemann-Pick Disease Type C2 Patient-Specific iPSCs Carrying the NPC2 Mutations c.58G>T/c.140G>T. . 2021-04-13. Pubmed ID: 33924575; DOI: 10.3390/ijms22084009; PMC: PMC8069078 AKOSi001-A 2021-04-13 2021-04-13 PubMed: 33924575 DOI: 10.3390/ijms22084009Associated cell lines:
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Li N, Yang F, Parthasarathy S, Pierre SS, Hong K, Pavon N, Pak C, Sun Y
Patterning Neuroepithelial Cell Sheet via a Sustained Chemical Gradient Generated by Localized Passive Diffusion Devices
Li N et al. Patterning Neuroepithelial Cell Sheet via a Sustained Chemical Gradient Generated by Localized Passive Diffusion Devices. . 2021-04-12. Pubmed ID: 33751893; DOI: 10.1021/acsbiomaterials.0c01365; PMC: PMC11146006 WAe009-A 2021-04-12 2021-04-12 PubMed: 33751893 DOI: 10.1021/acsbiomaterials.0c01365Associated cell lines:
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Hayder H, Fu G, Nadeem L, O'Brien JA, Lye SJ, Peng C
Overexpression of miR-210-3p Impairs Extravillous Trophoblast Functions Associated with Uterine Spiral Artery Remodeling
Hayder H et al. Overexpression of miR-210-3p Impairs Extravillous Trophoblast Functions Associated with Uterine Spiral Artery Remodeling. . 2021-04-12. Pubmed ID: 33921262; DOI: 10.3390/ijms22083961; PMC: PMC8069107 MHHi007-AMHHi007-A-1 2021-04-12 2021-04-12 PubMed: 33921262 DOI: 10.3390/ijms22083961Associated cell lines:
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Boyle L, Rao L, Kaur S, Fan X, Mebane C, Hamm L, Thornton A, Ahrendsen JT, Anderson MP, Christodoulou J, Gennerich A, Shen Y, Chung WK
Genotype and defects in microtubule-based motility correlate with clinical severity in KIF1A-associated neurological disorder
Boyle L et al. Genotype and defects in microtubule-based motility correlate with clinical severity in KIF1A-associated neurological disorder. . 2021-04-08. Pubmed ID: 33880452; DOI: 10.1016/j.xhgg.2021.100026; PMC: PMC8054982 SDUBMSi001-A 2021-04-08 2021-04-08 PubMed: 33880452 DOI: 10.1016/j.xhgg.2021.100026Associated cell lines:
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Yousefi R, Fornasiero EF, Cyganek L, Montoya J, Jakobs S, Rizzoli SO, Rehling P, Pacheu-Grau D
Monitoring mitochondrial translation in living cells
Yousefi R et al. Monitoring mitochondrial translation in living cells. . 2021-04-07. Pubmed ID: 33586863; DOI: 10.15252/embr.202051635; PMC: PMC8024989 UMGi130-A 2021-04-07 2021-04-07 PubMed: 33586863 DOI: 10.15252/embr.202051635Associated cell lines:
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Stelcer E, Kulcenty K, Rucinski M, Kruszyna-Mochalska M, Skrobala A, Sobecka A, Jopek K, Suchorska WM
Ionizing radiation exposure of stem cell-derived chondrocytes affects their gene and microRNA expression profiles and cytokine production
Stelcer E et al. Ionizing radiation exposure of stem cell-derived chondrocytes affects their gene and microRNA expression profiles and cytokine production. . 2021-04-05. Pubmed ID: 33820914; DOI: 10.1038/s41598-021-86230-1; PMC: PMC8021574 GPCCi001-A 2021-04-05 2021-04-05 PubMed: 33820914 DOI: 10.1038/s41598-021-86230-1Associated cell lines:
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Merkert S, Wunderlich S, Beier J, Franke A, Schwanke K, Göhring G, Kraft T, Francino A, Zweigerdt R, Martin U
Generation of two iPSC clones (MHHi021-A and MHHi021-B) from a patient with hypertrophic cardiomyopathy with p.Arg723Gly mutation in the MYH7 gene
Merkert S et al. Generation of two iPSC clones (MHHi021-A and MHHi021-B) from a patient with hypertrophic cardiomyopathy with p.Arg723Gly mutation in the MYH7 gene. . 2021-04-00. Pubmed ID: 33578365; DOI: 10.1016/j.scr.2021.102208 MHHi021-AMHHi021-B 2021-04-00 2021-04-00 PubMed: 33578365 DOI: 10.1016/j.scr.2021.102208 -
Silva TP, Pereira CA, Oliveira AR, Raposo AC, Arez M, Cabral JMS, Milagre I, Carmo-Fonseca M, da Rocha ST
Generation and characterization of induced pluripotent stem cells from a family carrying the BRCA1 mutation c.3612delA
Silva TP et al. Generation and characterization of induced pluripotent stem cells from a family carrying the BRCA1 mutation c.3612delA. . 2021-04-00. Pubmed ID: 33631522; DOI: 10.1016/j.scr.2021.102242 IBBISTi001-AIBBISTi001-BIBBISTi001-CIBBISTi001-DIBBISTi002-AIBBISTi002-B 2021-04-00 2021-04-00 PubMed: 33631522 DOI: 10.1016/j.scr.2021.102242Associated cell lines:
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Zhou T, Yang X, Chen Z, Zhou Y, Cao X, Zhao C, Zhao J
A novel COL2A1 mutation causing spondyloepiphyseal dysplasia congenita in a Chinese family
Zhou T et al. A novel COL2A1 mutation causing spondyloepiphyseal dysplasia congenita in a Chinese family. . 2021-04-00. Pubmed ID: 33590889; DOI: 10.1002/jcla.23728; PMC: PMC8059726 MCRIi001-B 2021-04-00 2021-04-00 PubMed: 33590889 DOI: 10.1002/jcla.23728Associated cell lines:
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Lu HE, Pan YL, Ko HW, Hsu SH, Wen CH, Hsu YC
Generation of induced pluripotent stem cells FIRDIi001-A from a Taiwanese subject carrying ALDH2 pE487K mutation
Lu HE et al. Generation of induced pluripotent stem cells FIRDIi001-A from a Taiwanese subject carrying ALDH2 pE487K mutation. . 2021-04-00. Pubmed ID: 33592568; DOI: 10.1016/j.scr.2021.102229 MMCi001-AFIRDIi001-A 2021-04-00 2021-04-00 PubMed: 33592568 DOI: 10.1016/j.scr.2021.102229Associated cell lines:
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Zhang C, Wei Y, Zhang Y, Zhang J, Xing Q, Zhou M, Shan Y
Establishment of a CRISPR/Cas9-mediated ANP32A homozygous knockout human embryonic stem cell line
Zhang C et al. Establishment of a CRISPR/Cas9-mediated ANP32A homozygous knockout human embryonic stem cell line. . 2021-04-00. Pubmed ID: 33607472; DOI: 10.1016/j.scr.2021.102234 WAe001-A-53 2021-04-00 2021-04-00 PubMed: 33607472 DOI: 10.1016/j.scr.2021.102234Associated cell lines:
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Tian X, Fu W, Guo G, Huang S, Dong Y, Li X, Dong J, Zhao X, Zhang Y
Generation of a human iPSC line ZZUNEUi015-A from a patient with hypertrophic cardiomyopathy caused by mutation in ALPK3
Tian X et al. Generation of a human iPSC line ZZUNEUi015-A from a patient with hypertrophic cardiomyopathy caused by mutation in ALPK3. . 2021-04-00. Pubmed ID: 33607470; DOI: 10.1016/j.scr.2021.102247 ZZUNEUi015-A 2021-04-00 2021-04-00 PubMed: 33607470 DOI: 10.1016/j.scr.2021.102247Associated cell lines:
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Zhang B
CRISPR/Cas gene therapy
Zhang B. CRISPR/Cas gene therapy. . 2021-04-00. Pubmed ID: 32959897; DOI: 10.1002/jcp.30064 ZSSYe001-A 2021-04-00 2021-04-00 PubMed: 32959897 DOI: 10.1002/jcp.30064Associated cell lines:
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Li Y, Dong R, Wang G, Zhang H, Yang X, Li Z, Guan J, Gai Z, Liu Y
Establishment of a novel human iPSC line (SDQLCHi032-A) derived from a patient with primary hypertrophic osteoarthropathy caused by HPGD homozygous mutation
Li Y et al. Establishment of a novel human iPSC line (SDQLCHi032-A) derived from a patient with primary hypertrophic osteoarthropathy caused by HPGD homozygous mutation. . 2021-04-00. Pubmed ID: 33550138; DOI: 10.1016/j.scr.2021.102217 SDQLCHi032-A 2021-04-00 2021-04-00 PubMed: 33550138 DOI: 10.1016/j.scr.2021.102217Associated cell lines:
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Yuan A, Tao R, Yu S, Jing N, Sun J
Generation of human induced pluripotent stem cell line FDCHDPi001-A from a Chinese Han Tourette's syndrome patient
Yuan A et al. Generation of human induced pluripotent stem cell line FDCHDPi001-A from a Chinese Han Tourette's syndrome patient. . 2021-04-00. Pubmed ID: 33607468; DOI: 10.1016/j.scr.2021.102227 FDCHDPi001-A 2021-04-00 2021-04-00 PubMed: 33607468 DOI: 10.1016/j.scr.2021.102227Associated cell lines:
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Skok K, Gradišnik L, Maver U, Kozar N, Sobočan M, Takač I, Arko D, Kavalar R
Gynaecological cancers and their cell lines
Skok K et al. Gynaecological cancers and their cell lines. . 2021-04-00. Pubmed ID: 33650759; DOI: 10.1111/jcmm.16397; PMC: PMC8051715 KMUe003-A 2021-04-00 2021-04-00 PubMed: 33650759 DOI: 10.1111/jcmm.16397Associated cell lines:
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Laverde-Paz MJ, Nuytemans K, Wang L, Vance JM, Pericak-Vance MA, Dykxhoorn DM, Cukier HN
Derivation of stem cell line UMi028-A-2 containing a CRISPR/Cas9 induced Alzheimer's disease risk variant p.S1038C in the TTC3 gene
Laverde-Paz MJ et al. Derivation of stem cell line UMi028-A-2 containing a CRISPR/Cas9 induced Alzheimer's disease risk variant p.S1038C in the TTC3 gene. . 2021-04-00. Pubmed ID: 33626494; DOI: 10.1016/j.scr.2021.102258 UMi028-AUMi028-A-2 2021-04-00 2021-04-00 PubMed: 33626494 DOI: 10.1016/j.scr.2021.102258Associated cell lines:
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Hong W, Yun W, Choi W, Son D, Song G, You S
Generation of a WA14 hESC sub-line carrying a hemizygous ABCD1 (C.1696_1710 del) mutation introduced by CRISPR/Cas9 technology
Hong W et al. Generation of a WA14 hESC sub-line carrying a hemizygous ABCD1 (C.1696_1710 del) mutation introduced by CRISPR/Cas9 technology. . 2021-04-00. Pubmed ID: 33611043; DOI: 10.1016/j.scr.2021.102244 WAe014-A-1 2021-04-00 2021-04-00 PubMed: 33611043 DOI: 10.1016/j.scr.2021.102244Associated cell lines:
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Yi C, Dingya C, Nengqing L, Hongmei G, Yi L, Huimin Z, Jiajia X, Bing S, Xiaofang S
Generation of induced pluripotent stem cell GZHMCi005-A from amniotic fluid-derived cells with duplication of chromosome 8p
Yi C et al. Generation of induced pluripotent stem cell GZHMCi005-A from amniotic fluid-derived cells with duplication of chromosome 8p. . 2021-04-00. Pubmed ID: 33588214; DOI: 10.1016/j.scr.2021.102226 GZHMCi005-A 2021-04-00 2021-04-00 PubMed: 33588214 DOI: 10.1016/j.scr.2021.102226Associated cell lines:
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Guo X, Wang D, Shan X, Yang L, Ding Y, Chen H, Rong X, Chu M, Lin J, Chen C
Establishment of an induced pluripotent stem cell line from a Antley-Bixler Syndrome (ABS) patient with the homozygote mutation p.R457H (c.1370G>A) in POR gene
Guo X et al. Establishment of an induced pluripotent stem cell line from a Antley-Bixler Syndrome (ABS) patient with the homozygote mutation p.R457H (c.1370G>A) in POR gene. . 2021-04-00. Pubmed ID: 33631521; DOI: 10.1016/j.scr.2021.102261 WMUi018-A 2021-04-00 2021-04-00 PubMed: 33631521 DOI: 10.1016/j.scr.2021.102261Associated cell lines:
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Tangprasittipap A, Chumchuen S, Pornratananont G, Kitiyanant N, Hongeng S
Generation of a human induced pluripotent stem cells (MUi015-A) from skin fibroblast of retinoblastoma patient with 13q deletion syndrome
Tangprasittipap A et al. Generation of a human induced pluripotent stem cells (MUi015-A) from skin fibroblast of retinoblastoma patient with 13q deletion syndrome. . 2021-04-00. Pubmed ID: 33550139; DOI: 10.1016/j.scr.2021.102211 MUi015-A 2021-04-00 2021-04-00 PubMed: 33550139 DOI: 10.1016/j.scr.2021.102211Associated cell lines:
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Witt G, Keminer O, Leu J, Tandon R, Meiser I, Willing A, Winschel I, Abt JC, Brändl B, Sébastien I, Friese MA, Müller FJ, Neubauer JC, Claussen C, Zimmermann H, Gribbon P, Pless O
An automated and high-throughput-screening compatible pluripotent stem cell-based test platform for developmental and reproductive toxicity assessment of small molecule compounds
Witt G et al. An automated and high-throughput-screening compatible pluripotent stem cell-based test platform for developmental and reproductive toxicity assessment of small molecule compounds. . 2021-04-00. Pubmed ID: 32564278; DOI: 10.1007/s10565-020-09538-0; PMC: PMC8012336 ZIPi013-BZIPi013-E 2021-04-00 2021-04-00 PubMed: 32564278 DOI: 10.1007/s10565-020-09538-0 -
Sawangareetrakul P, Ngiwsara L, Champattanachai V, Chokchaichamnankit D, Saharat K, Ketudat Cairns JR, Srisomsap C, Khwanraj K, Dharmasaroja P, Pulkes T, Svasti J
Aberrant proteins expressed in skin fibroblasts of Parkinson's disease patients carrying heterozygous variants of glucocerebrosidase and parkin genes
Sawangareetrakul P et al. Aberrant proteins expressed in skin fibroblasts of Parkinson's disease patients carrying heterozygous variants of glucocerebrosidase and parkin genes. . 2021-04-00. Pubmed ID: 33732455; DOI: 10.3892/br.2021.1412; PMC: PMC7907964 RCPCMi004-A 2021-04-00 2021-04-00 PubMed: 33732455 DOI: 10.3892/br.2021.1412Associated cell lines:
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Haase A, Kohrn T, Fricke V, Ricci Signorini ME, Witte M, Göhring G, Gruh I, Martin U
Establishment of MHHi001-A-5, a GCaMP6f and RedStar dual reporter human iPSC line for in vitro and in vivo characterization and in situ tracing of iPSC derivatives
Haase A et al. Establishment of MHHi001-A-5, a GCaMP6f and RedStar dual reporter human iPSC line for in vitro and in vivo characterization and in situ tracing of iPSC derivatives. . 2021-04-00. Pubmed ID: 33571874; DOI: 10.1016/j.scr.2021.102206 MHHi001-AMHHi001-A-5 2021-04-00 2021-04-00 PubMed: 33571874 DOI: 10.1016/j.scr.2021.102206Associated cell lines:
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Liszewska E, Majchrowicz L, Krogulec E, Kotulska K, Kaczmarek L, Kalita K, Dobrzyń A, Jaworski J
Establishment of two hiPSC lines (IIMCBi001-A and IIMCBi002-A) from dermal fibroblasts of healthy donors and characterization of their cell cycle
Liszewska E et al. Establishment of two hiPSC lines (IIMCBi001-A and IIMCBi002-A) from dermal fibroblasts of healthy donors and characterization of their cell cycle. . 2021-04-00. Pubmed ID: 33588215; DOI: 10.1016/j.scr.2021.102225 IIMCBi001-AIIMCBi002-A 2021-04-00 2021-04-00 PubMed: 33588215 DOI: 10.1016/j.scr.2021.102225Associated cell lines:
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Guo J, Fang F, Dai Q, Zhang W, Di W, Hu J, Zhao J, Cao J, Wang Y
Generation of a human-derived induced pluripotent stem cell line (SIAISi012-A) from an 82-year-old healthy Chinese Han male
Guo J et al. Generation of a human-derived induced pluripotent stem cell line (SIAISi012-A) from an 82-year-old healthy Chinese Han male. . 2021-04-00. Pubmed ID: 33610016; DOI: 10.1016/j.scr.2021.102186 SIAISi012-A 2021-04-00 2021-04-00 PubMed: 33610016 DOI: 10.1016/j.scr.2021.102186Associated cell lines:
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Hedges EC, Topp S, Shaw CE, Nishimura AL
Generation of six induced pluripotent stem cell lines from patients with amyotrophic lateral sclerosis with associated genetic mutations in either FUS or ANXA11
Hedges EC et al. Generation of six induced pluripotent stem cell lines from patients with amyotrophic lateral sclerosis with associated genetic mutations in either FUS or ANXA11. . 2021-04-00. Pubmed ID: 33610019; DOI: 10.1016/j.scr.2021.102246; PMC: PMC7988463 KCLi008-AKCLi009-AKCLi010-AKCLi011-AKCLi012-AKCLi013-A 2021-04-00 2021-04-00 PubMed: 33610019 DOI: 10.1016/j.scr.2021.102246 -
Kondrateva E, Demchenko A, Slesarenko Y, Pozhitnova V, Yasinovsky M, Amelina E, Tabakov V, Voronina E, Lavrov A, Smirnikhina S
Generation of two induced pluripotent stem cell lines (RCMGi004-A and -B) from human skin fibroblasts of a cystic fibrosis patient with compound heterozygous F508del/W1282X mutations in CFTR gene
Kondrateva E et al. Generation of two induced pluripotent stem cell lines (RCMGi004-A and -B) from human skin fibroblasts of a cystic fibrosis patient with compound heterozygous F508del/W1282X mutations in CFTR gene. . 2021-04-00. Pubmed ID: 33607467; DOI: 10.1016/j.scr.2021.102232 RCMGi004-ARCMGi004-B 2021-04-00 2021-04-00 PubMed: 33607467 DOI: 10.1016/j.scr.2021.102232Associated cell lines:
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Ji W, Wang D, Chen C, Chen H, Ding Y, Li C, Rong X, Shan X, Chu M, Shen X, Guo X
Generation of an induced pluripotent stem cell line from a Bartter syndrome patient with the homozygote mutation p.A244D (c.731C>A) in SLC12A1 gene
Ji W et al. Generation of an induced pluripotent stem cell line from a Bartter syndrome patient with the homozygote mutation p.A244D (c.731C>A) in SLC12A1 gene. . 2021-04-00. Pubmed ID: 33607471; DOI: 10.1016/j.scr.2021.102228 WMUi019-A 2021-04-00 2021-04-00 PubMed: 33607471 DOI: 10.1016/j.scr.2021.102228Associated cell lines:
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Huang S, Fu W, Guo G, Tiana X, Zhao X, Dong J, Li X, Yang H
Generation of a hiPSC line ZZUNEUi017-A from a patient with dilated cardiomyopathy caused by mutation in TTN
Huang S et al. Generation of a hiPSC line ZZUNEUi017-A from a patient with dilated cardiomyopathy caused by mutation in TTN. . 2021-04-00. Pubmed ID: 33610015; DOI: 10.1016/j.scr.2021.102248 ZZUSAHi002-AZZUNEUi017-A 2021-04-00 2021-04-00 PubMed: 33610015 DOI: 10.1016/j.scr.2021.102248Associated cell lines:
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Guan J, Yan B, Zhang H, Liu C, Li Y, Yang X, Li Z, Gai Z, Liu Y
Generation of a human induced pluripotent stem cell line (SDQLCHi036-A) from a patient with ornithine transcarbamylase deficiency carrying a deletion involving 3-9 exons of OTC gene
Guan J et al. Generation of a human induced pluripotent stem cell line (SDQLCHi036-A) from a patient with ornithine transcarbamylase deficiency carrying a deletion involving 3-9 exons of OTC gene. . 2021-04-00. Pubmed ID: 33550136; DOI: 10.1016/j.scr.2021.102220 SDQLCHi036-A 2021-04-00 2021-04-00 PubMed: 33550136 DOI: 10.1016/j.scr.2021.102220Associated cell lines:
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Paes BCMF, Stabeli LCJR, Costa PNM, Orellana MD, Kashima S, Covas DT, Picanço-Castro V
Generation of hematopoietic stem/progenitor cells with sickle cell mutation from induced pluripotent stem cell in serum-free system
Paes BCMF et al. Generation of hematopoietic stem/progenitor cells with sickle cell mutation from induced pluripotent stem cell in serum-free system. . 2021-04-00. Pubmed ID: 32229108; DOI: 10.1016/j.htct.2020.01.005; PMC: PMC8211631 WAe001-A 2021-04-00 2021-04-00 PubMed: 32229108 DOI: 10.1016/j.htct.2020.01.005Associated cell lines:
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Fontaine V, Duboscq-Bidot L, Jouve C, Hamlin M, Curjol A, Briand V, Janiak P, Hulot JS, Pruniaux-Harnist MP, Charron P, Villard E
Generation of iPSC line from MYH7 R403L mutation carrier with severe hypertrophic cardiomyopathy and isogenic CRISPR/Cas9 corrected control
Fontaine V et al. Generation of iPSC line from MYH7 R403L mutation carrier with severe hypertrophic cardiomyopathy and isogenic CRISPR/Cas9 corrected control. . 2021-04-00. Pubmed ID: 33610018; DOI: 10.1016/j.scr.2021.102245 ICANi001-AICANi001-A-1 2021-04-00 2021-04-00 PubMed: 33610018 DOI: 10.1016/j.scr.2021.102245Associated cell lines:
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Huang Y, Wu H, Han X, Wu J, Yu M, Zhao ZA, Shen Z, Hu S, Lei W
Generation of an EFNB2-2A-mCherry reporter human embryonic stem cell line using CRISPR/Cas9-mediated site-specific homologous recombination
Huang Y et al. Generation of an EFNB2-2A-mCherry reporter human embryonic stem cell line using CRISPR/Cas9-mediated site-specific homologous recombination. . 2021-04-00. Pubmed ID: 33611045; DOI: 10.1016/j.scr.2021.102241 WAe001-AWAe001-A-57 2021-04-00 2021-04-00 PubMed: 33611045 DOI: 10.1016/j.scr.2021.102241Associated cell lines:
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Guan J, Tian G, Dong R, Zhang H, Yang X, Li Y, Gai Z, Liu Y
Induced pluripotent stem cell line (SDQLCHi041-A) from a male patient with mucopolysaccharidosis type IIIB
Guan J et al. Induced pluripotent stem cell line (SDQLCHi041-A) from a male patient with mucopolysaccharidosis type IIIB. . 2021-04-00. Pubmed ID: 33550137; DOI: 10.1016/j.scr.2021.102212 SDQLCHi021-ASDQLCHi041-A 2021-04-00 2021-04-00 PubMed: 33550137 DOI: 10.1016/j.scr.2021.102212Associated cell lines:
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Ma Y, Wang Z, Liu X, Sun W, Gong Y, Liu G, Sun G
Generation and characterization of an integration-free iPSC line SDUBMSi006-A from a patient with Alport syndrome caused by COL4A3 gene mutations
Ma Y et al. Generation and characterization of an integration-free iPSC line SDUBMSi006-A from a patient with Alport syndrome caused by COL4A3 gene mutations. . 2021-04-00. Pubmed ID: 33601099; DOI: 10.1016/j.scr.2021.102237 SDUBMSi006-A 2021-04-00 2021-04-00 PubMed: 33601099 DOI: 10.1016/j.scr.2021.102237Associated cell lines:
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Ding Y, O'Brien A, de la Cruz BM, Yang M, Fitzgerald J, Yang G, Li W, McInerney V, Krawczyk J, Lynch SA, Howard L, Allen NM, O'Brien T, Gallagher L, Shen S
Derivation of iPSC lines from two patients with autism spectrum disorder carrying NRXN1α deletion (NUIGi041-A, NUIG041-B; NUIGi045-A) and one sibling control (NUIGi042-A, NUIGi042-B)
Ding Y et al. Derivation of iPSC lines from two patients with autism spectrum disorder carrying NRXN1α deletion (NUIGi041-A, NUIG041-B; NUIGi045-A) and one sibling control (NUIGi042-A, NUIGi042-B). . 2021-04-00. Pubmed ID: 33578364; DOI: 10.1016/j.scr.2021.102222 NUIGi041-ANUIGi042-ANUIGi045-ANUIGi041-BNUIGi042-B 2021-04-00 2021-04-00 PubMed: 33578364 DOI: 10.1016/j.scr.2021.102222Associated cell lines:
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Schmid B, Holst B, Poulsen U, Jørring I, Clausen C, Rasmussen M, Mau-Holzmann UA, Steeg R, Nuthall H, Ebneth A, Cabrera-Socorro A
Generation of two gene edited iPSC-lines carrying a DOX-inducible NGN2 expression cassette with and without GFP in the AAVS1 locus
Schmid B et al. Generation of two gene edited iPSC-lines carrying a DOX-inducible NGN2 expression cassette with and without GFP in the AAVS1 locus. . 2021-04-00. Pubmed ID: 33610017; DOI: 10.1016/j.scr.2021.102240 BIONi010-CBIONi010-C-13BIONi010-C-15 2021-04-00 2021-04-00 PubMed: 33610017 DOI: 10.1016/j.scr.2021.102240Associated cell lines:
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Fan Y, Liu F, Fan LY, Mao CY, Liu H, Zhang C, Yuan YP, Yang J, Wang YL, Liu YT, Shi CH, Xu YM
Generation of an induced pluripotent stem cell line (ZZUi020-A) from a patient with Parkinson's disease harboring the intermediate-length GGC repeat expansions in the NOTCH2NLC gene
Fan Y et al. Generation of an induced pluripotent stem cell line (ZZUi020-A) from a patient with Parkinson's disease harboring the intermediate-length GGC repeat expansions in the NOTCH2NLC gene. . 2021-04-00. Pubmed ID: 33626493; DOI: 10.1016/j.scr.2021.102257 ZZUi020-AZZUi037-A 2021-04-00 2021-04-00 PubMed: 33626493 DOI: 10.1016/j.scr.2021.102257 -
Schmid B, Holst B, Clausen C, Bahnassawy L, Reinhardt P, Bakker MHM, Díaz-Guerra E, Vicario C, Martino-Adami PV, Thoenes M, Ramirez A, Fliessbach K, Grezella C, Brüstle O, Peitz M, Ebneth A, Cabrera-Socorro A
Generation of a set of isogenic iPSC lines carrying all APOE genetic variants (Ɛ2/Ɛ3/Ɛ4) and knock-out for the study of APOE biology in health and disease
Schmid B et al. Generation of a set of isogenic iPSC lines carrying all APOE genetic variants (Ɛ2/Ɛ3/Ɛ4) and knock-out for the study of APOE biology in health and disease. . 2021-04-00. Pubmed ID: 33556820; DOI: 10.1016/j.scr.2021.102180 UKBi011-AUKBi011-A-1UKBi011-A-2UKBi011-A-3UKBi011-A-4 2021-04-00 2021-04-00 PubMed: 33556820 DOI: 10.1016/j.scr.2021.102180Associated cell lines:
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Gonsior K, Kaucher GA, Pelz P, Schumann D, Gansel M, Kuhs S, Klockgether T, Forlani S, Durr A, Hauser S, Rattay TW, Synofzik M, Hengel H, Schöls L, Rieß OH, Hübener-Schmid J
PolyQ-expanded ataxin-3 protein levels in peripheral blood mononuclear cells correlate with clinical parameters in SCA3: a pilot study
Gonsior K et al. PolyQ-expanded ataxin-3 protein levels in peripheral blood mononuclear cells correlate with clinical parameters in SCA3: a pilot study. . 2021-04-00. Pubmed ID: 33106888; DOI: 10.1007/s00415-020-10274-y; PMC: PMC7990753 HIHCNi002-A 2021-04-00 2021-04-00 PubMed: 33106888 DOI: 10.1007/s00415-020-10274-yAssociated cell lines:
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Sun X, Zhou X, Dong B, Wang C, Xiao X, Wang Y
Generation of a gene-corrected isogenic iPSC line (AHQUi001-A-1) from a patient with familial hypertriglyceridemia (FHTG) carrying a heterozygous p.C310R (c.928 T > C) mutation in LPL gene using CRISPR/Cas9
Sun X et al. Generation of a gene-corrected isogenic iPSC line (AHQUi001-A-1) from a patient with familial hypertriglyceridemia (FHTG) carrying a heterozygous p.C310R (c.928 T > C) mutation in LPL gene using CRISPR/Cas9. . 2021-04-00. Pubmed ID: 33592566; DOI: 10.1016/j.scr.2021.102230 AHQUi001-AAHQUi001-A-1 2021-04-00 2021-04-00 PubMed: 33592566 DOI: 10.1016/j.scr.2021.102230Associated cell lines:
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Han HJ, Kim JH
Establishment of a TLR3 homozygous knockout human induced pluripotent stem cell line using CRISPR/Cas9
Han HJ et al. Establishment of a TLR3 homozygous knockout human induced pluripotent stem cell line using CRISPR/Cas9. . 2021-04-00. Pubmed ID: 33582546; DOI: 10.1016/j.scr.2021.102187 KSCBi005-AKSCBi005-A-5KSCBi005-A-6 2021-04-00 2021-04-00 PubMed: 33582546 DOI: 10.1016/j.scr.2021.102187Associated cell lines:
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Campostrini G, Meraviglia V, Giacomelli E, van Helden RWJ, Yiangou L, Davis RP, Bellin M, Orlova VV, Mummery CL
Generation, functional analysis and applications of isogenic three-dimensional self-aggregating cardiac microtissues from human pluripotent stem cells
Campostrini G et al. Generation, functional analysis and applications of isogenic three-dimensional self-aggregating cardiac microtissues from human pluripotent stem cells. . 2021-04-00. Pubmed ID: 33772245; DOI: 10.1038/s41596-021-00497-2; PMC: PMC7611409 LUMCi004-ALUMCi027-ALUMCi028-A 2021-04-00 2021-04-00 PubMed: 33772245 DOI: 10.1038/s41596-021-00497-2Associated cell lines:
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Fogerty J, Perkins BD
Knockout of the CEP290 gene in human induced pluripotent stem cells
Fogerty J et al. Knockout of the CEP290 gene in human induced pluripotent stem cells. . 2021-04-00. Pubmed ID: 33626495; DOI: 10.1016/j.scr.2021.102243; PMC: PMC8127132 CEIi001-A 2021-04-00 2021-04-00 PubMed: 33626495 DOI: 10.1016/j.scr.2021.102243Associated cell lines:
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Sims CHC, Autio MI, Buskin A, Cheung C, Heer R, Foo RSY, Wang X
Modified CRISPR/Cas9 mediated generation of two MKK7 knockout human embryonic stem cell lines
Sims CHC et al. Modified CRISPR/Cas9 mediated generation of two MKK7 knockout human embryonic stem cell lines. . 2021-04-00. Pubmed ID: 33611044; DOI: 10.1016/j.scr.2021.102238 WAe001-AWAe001-A-54WAe001-A-55 2021-04-00 2021-04-00 PubMed: 33611044 DOI: 10.1016/j.scr.2021.102238Associated cell lines:
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Guo Y, Wang J, Wang Z, Lou Y, Chen W, Sheng M, Wang Y, Zhang B, Gao L, Feng J
Establishment of an induced pluripotent stem cell line (ZJSHi001-A) from a patient with epileptic encephalopathy carrying KCNB1 Glu330Asp mutation
Guo Y et al. Establishment of an induced pluripotent stem cell line (ZJSHi001-A) from a patient with epileptic encephalopathy carrying KCNB1 Glu330Asp mutation. . 2021-04-00. Pubmed ID: 33607466; DOI: 10.1016/j.scr.2021.102224 ZJSHi001-A 2021-04-00 2021-04-00 PubMed: 33607466 DOI: 10.1016/j.scr.2021.102224Associated cell lines:
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Zaepfel BL, Zhang Z, Maulding K, Coyne AN, Cheng W, Hayes LR, Lloyd TE, Sun S, Rothstein JD
UPF1 reduces C9orf72 HRE-induced neurotoxicity in the absence of nonsense-mediated decay dysfunction
Zaepfel BL et al. UPF1 reduces C9orf72 HRE-induced neurotoxicity in the absence of nonsense-mediated decay dysfunction. . 2021-03-30. Pubmed ID: 33789100; DOI: 10.1016/j.celrep.2021.108925; PMC: PMC8063722 EDi036-A 2021-03-30 2021-03-30 PubMed: 33789100 DOI: 10.1016/j.celrep.2021.108925Associated cell lines:
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Rufaihah AJ, Chen CK, Yap CH, Mattar CNZ
Mending a broken heart: In vitro, in vivo and in silico models of congenital heart disease
Rufaihah AJ et al. Mending a broken heart: In vitro, in vivo and in silico models of congenital heart disease. . 2021-03-28. Pubmed ID: 33787508; DOI: 10.1242/dmm.047522; PMC: PMC8033415 YAHKMUi001-A 2021-03-28 2021-03-28 PubMed: 33787508 DOI: 10.1242/dmm.047522Associated cell lines:
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Elsayed AK, Vimalraj S, Nandakumar M, Abdelalim EM
Insulin resistance in diabetes: The promise of using induced pluripotent stem cell technology
Elsayed AK et al. Insulin resistance in diabetes: The promise of using induced pluripotent stem cell technology. . 2021-03-26. Pubmed ID: 33815671; DOI: 10.4252/wjsc.v13.i3.221; PMC: PMC8006014 QBRIi007-A 2021-03-26 2021-03-26 PubMed: 33815671 DOI: 10.4252/wjsc.v13.i3.221Associated cell lines:
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Antonov SA, Novosadova EV
Current State-of-the-Art and Unresolved Problems in Using Human Induced Pluripotent Stem Cell-Derived Dopamine Neurons for Parkinson's Disease Drug Development
Antonov SA et al. Current State-of-the-Art and Unresolved Problems in Using Human Induced Pluripotent Stem Cell-Derived Dopamine Neurons for Parkinson's Disease Drug Development. . 2021-03-25. Pubmed ID: 33806103; DOI: 10.3390/ijms22073381; PMC: PMC8037675 GIBHi003-ARCPCMi004-A 2021-03-25 2021-03-25 PubMed: 33806103 DOI: 10.3390/ijms22073381Associated cell lines:
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Caengprasath N, Theerapanon T, Porntaveetus T, Shotelersuk V
MBTPS2, a membrane bound protease, underlying several distinct skin and bone disorders
Caengprasath N et al. MBTPS2, a membrane bound protease, underlying several distinct skin and bone disorders. . 2021-03-20. Pubmed ID: 33743732; DOI: 10.1186/s12967-021-02779-5; PMC: PMC7981912 MDCUi001-AMDCUi001-B 2021-03-20 2021-03-20 PubMed: 33743732 DOI: 10.1186/s12967-021-02779-5Associated cell lines:
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Magusali Naciye, Graham Andrew C., Piers Thomas M., Panichnantakul Pantila, Yaman Umran, Shoai Maryam, Reynolds Regina H., Botia Juan A., Brookes Keeley J., Guetta-Baranes Tamar, Bellou Eftychia, Bayram Sevinc, Sokolova Dimitra, Ryten Mina, Frigerio Carlo Sala, Escott-Price Valentina, Morgan Kevin, Pocock Jennifer M., Hardy John, Salih Dervis A.
Genetic variability associated withOAS1expression in myeloid cells increases the risk of Alzheimer’s disease and severe COVID-19 outcomes
Magusali Naciye et al. Genetic variability associated withOAS1expression in myeloid cells increases the risk of Alzheimer’s disease and severe COVID-19 outcomes. . 2021-03-18. DOI: 10.1101/2021.03.16.435702 BIONi010-C 2021-03-18 2021-03-18 DOI: 10.1101/2021.03.16.435702Associated cell lines:
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Kong D, Feng B, Amponsah AE, He J, Guo R, Liu B, Du X, Liu X, Zhang S, Lv F, Ma J, Cui H
hiPSC-derived NSCs effectively promote the functional recovery of acute spinal cord injury in mice
Kong D et al. hiPSC-derived NSCs effectively promote the functional recovery of acute spinal cord injury in mice. . 2021-03-11. Pubmed ID: 33706803; DOI: 10.1186/s13287-021-02217-9; PMC: PMC7953804 HEBHMUi002-A 2021-03-11 2021-03-11 PubMed: 33706803 DOI: 10.1186/s13287-021-02217-9Associated cell lines:
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Döring JH, Schröter J, Jüngling J, Biskup S, Klotz KA, Bast T, Dietel T, Korenke GC, Christoph S, Brennenstuhl H, Rubboli G, Møller RS, Lesca G, Chaix Y, Kölker S, Hoffmann GF, Lemke JR, Syrbe S
Refining Genotypes and Phenotypes in KCNA2-Related Neurological Disorders
Döring JH et al. Refining Genotypes and Phenotypes in KCNA2-Related Neurological Disorders. . 2021-03-10. Pubmed ID: 33802230; DOI: 10.3390/ijms22062824; PMC: PMC7999221 HIHDNEi002-AHIHDNEi003-A 2021-03-10 2021-03-10 PubMed: 33802230 DOI: 10.3390/ijms22062824Associated cell lines:
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Lester Sequiera G, Srivastava A, Alagarsamy KN, Rockman-Greenberg C, Dhingra S
Generation and Evaluation of Isogenic iPSC as a Source of Cell Replacement Therapies in Patients with Kearns Sayre Syndrome
Lester Sequiera G et al. Generation and Evaluation of Isogenic iPSC as a Source of Cell Replacement Therapies in Patients with Kearns Sayre Syndrome. . 2021-03-05. Pubmed ID: 33807701; DOI: 10.3390/cells10030568; PMC: PMC7998189 UOMi002-AUOMi005-AUOMi006-A 2021-03-05 2021-03-05 PubMed: 33807701 DOI: 10.3390/cells10030568 -
Diakatou M, Dubois G, Erkilic N, Sanjurjo-Soriano C, Meunier I, Kalatzis V
Allele-Specific Knockout by CRISPR/Cas to Treat Autosomal Dominant Retinitis Pigmentosa Caused by the G56R Mutation in NR2E3
Diakatou M et al. Allele-Specific Knockout by CRISPR/Cas to Treat Autosomal Dominant Retinitis Pigmentosa Caused by the G56R Mutation in NR2E3. . 2021-03-05. Pubmed ID: 33807610; DOI: 10.3390/ijms22052607; PMC: PMC7961898 INMi003-AINMi004-A 2021-03-05 2021-03-05 PubMed: 33807610 DOI: 10.3390/ijms22052607 -
Nilsri N, Jangprasert P, Pawinwongchai J, Israsena N, Rojnuckarin P
Distinct effects of V617F and exon12-mutated JAK2 expressions on erythropoiesis in a human induced pluripotent stem cell (iPSC)-based model
Nilsri N et al. Distinct effects of V617F and exon12-mutated JAK2 expressions on erythropoiesis in a human induced pluripotent stem cell (iPSC)-based model. . 2021-03-04. Pubmed ID: 33664283; DOI: 10.1038/s41598-021-83895-6; PMC: PMC7933160 ASUi001-AASUi002-A 2021-03-04 2021-03-04 PubMed: 33664283 DOI: 10.1038/s41598-021-83895-6 -
Hornig NC, Holterhus PM
Molecular basis of androgen insensitivity syndromes
Hornig NC et al. Molecular basis of androgen insensitivity syndromes. . 2021-03-01. Pubmed ID: 33385475; DOI: 10.1016/j.mce.2020.111146 SKLRMi001-A 2021-03-01 2021-03-01 PubMed: 33385475 DOI: 10.1016/j.mce.2020.111146Associated cell lines:
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Zhang W, Dai Q, Hua Y, Di W, Guo J, Zhao J, Deng Y, Wang Y
Generation of three iPSC cell lines (SIAISi006-A, SIAISi007-A and SIAISi008-A) from a 66-year-old Alzheimer's disease (AD) patient and her two unaffected children from Chinese Han population
Zhang W et al. Generation of three iPSC cell lines (SIAISi006-A, SIAISi007-A and SIAISi008-A) from a 66-year-old Alzheimer's disease (AD) patient and her two unaffected children from Chinese Han population. . 2021-03-00. Pubmed ID: 33472125; DOI: 10.1016/j.scr.2021.102172 SIAISi006-ASIAISi007-ASIAISi008-A 2021-03-00 2021-03-00 PubMed: 33472125 DOI: 10.1016/j.scr.2021.102172Associated cell lines:
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Madrid M, Sumen C, Aivio S, Saklayen N
Autologous Induced Pluripotent Stem Cell-Based Cell Therapies: Promise, Progress, and Challenges
Madrid M et al. Autologous Induced Pluripotent Stem Cell-Based Cell Therapies: Promise, Progress, and Challenges. . 2021-03-00. Pubmed ID: 33725407; DOI: 10.1002/cpz1.88 NYGCe001-A 2021-03-00 2021-03-00 PubMed: 33725407 DOI: 10.1002/cpz1.88Associated cell lines:
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Tang BL
RAB39B's role in membrane traffic, autophagy, and associated neuropathology
Tang BL. RAB39B's role in membrane traffic, autophagy, and associated neuropathology. . 2021-03-00. Pubmed ID: 32761840; DOI: 10.1002/jcp.29962 ZZUi005-A 2021-03-00 2021-03-00 PubMed: 32761840 DOI: 10.1002/jcp.29962Associated cell lines:
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Guo J, Di W, Zhang W, Dai Q, Zhao J, Deng Y, Wang Y
Generation of an induced pluripotent stem cell line (SIAISi009-A) from a 60-year-old Chinese Han female with mild cognitive impairment (MCI) having two copies of APOE4/4 allele
Guo J et al. Generation of an induced pluripotent stem cell line (SIAISi009-A) from a 60-year-old Chinese Han female with mild cognitive impairment (MCI) having two copies of APOE4/4 allele. . 2021-03-00. Pubmed ID: 33524675; DOI: 10.1016/j.scr.2021.102198 SIAISi009-A 2021-03-00 2021-03-00 PubMed: 33524675 DOI: 10.1016/j.scr.2021.102198Associated cell lines:
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Wang Guang-Bin, Rao Ni-Ni, Dong Chang-Long, Lyu Xiao-Qin
Identification of the potential function of circRNA in hypertrophic cardiomyopathy based on mutual RNA-RNA and RNA-RBP relationships shown by microarray data
Wang Guang-Bin et al. Identification of the potential function of circRNA in hypertrophic cardiomyopathy based on mutual RNA-RNA and RNA-RBP relationships shown by microarray data. . 2021-03-00. DOI: 10.1016/j.jnlest.2021.100097 WAe009-AWAe009-A-36 2021-03-00 2021-03-00 DOI: 10.1016/j.jnlest.2021.100097Associated cell lines:
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Ou-Yang CH, Tai CH, Lin HY, Huang CY, Lin CH
Generation of a human induced pluripotent stem cell (iPSC) line (IBMS-iPSC-070-02) from a patient with neurodegeneration with brain iron accumulation (NBIA) having compound heterozygous mutations in PANK2 gene
Ou-Yang CH et al. Generation of a human induced pluripotent stem cell (iPSC) line (IBMS-iPSC-070-02) from a patient with neurodegeneration with brain iron accumulation (NBIA) having compound heterozygous mutations in PANK2 gene. . 2021-03-00. Pubmed ID: 33517123; DOI: 10.1016/j.scr.2021.102190 IBMSi025-A 2021-03-00 2021-03-00 PubMed: 33517123 DOI: 10.1016/j.scr.2021.102190Associated cell lines:
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Ghanami Gashti N, Sadighi Gilani MA, Abbasi M
Sertoli cell-only syndrome: etiology and clinical management
Ghanami Gashti N et al. Sertoli cell-only syndrome: etiology and clinical management. . 2021-03-00. Pubmed ID: 33428073; DOI: 10.1007/s10815-021-02063-x; PMC: PMC7910341 HUSTi002-A 2021-03-00 2021-03-00 PubMed: 33428073 DOI: 10.1007/s10815-021-02063-xAssociated cell lines:
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Yang X, Wu F, Zhong J, Li F
Establishment of human embryonic stem cell WAe009-A-48 carrying a long QT syndrome mutation in SCN5A
Yang X et al. Establishment of human embryonic stem cell WAe009-A-48 carrying a long QT syndrome mutation in SCN5A. . 2021-03-00. Pubmed ID: 33517120; DOI: 10.1016/j.scr.2021.102194 WAe009-AWAe009-A-48 2021-03-00 2021-03-00 PubMed: 33517120 DOI: 10.1016/j.scr.2021.102194Associated cell lines:
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Rabinski T, Sagiv ST, Hausman-Kedem M, Fattal-Valevski A, Rubinstein M, Avraham KB, Vatine GD
Reprogramming of two induced pluripotent stem cell lines from a heterozygous GRIN2D developmental and epileptic encephalopathy (DEE) patient (BGUi011-A) and from a healthy family relative (BGUi012-A)
Rabinski T et al. Reprogramming of two induced pluripotent stem cell lines from a heterozygous GRIN2D developmental and epileptic encephalopathy (DEE) patient (BGUi011-A) and from a healthy family relative (BGUi012-A). . 2021-03-00. Pubmed ID: 33482465; DOI: 10.1016/j.scr.2021.102178 BGUi001-ABGUi002-ABGUi003-ABGUi004-ABGUi005-ABGUi011-ABGUi012-A 2021-03-00 2021-03-00 PubMed: 33482465 DOI: 10.1016/j.scr.2021.102178 -
Yang X, Duan C, Zhang H, Li Y, Guan J, Wang D, Lv Y, Gai Z, Liu Y
Establishment of a non-integrate iPS cell line (SDQLCHi023-A) from a patient with Xq25 microduplication syndrome carrying a 1.3 Mb hemizygote duplication at chrXq25
Yang X et al. Establishment of a non-integrate iPS cell line (SDQLCHi023-A) from a patient with Xq25 microduplication syndrome carrying a 1.3 Mb hemizygote duplication at chrXq25. . 2021-03-00. Pubmed ID: 33493992; DOI: 10.1016/j.scr.2020.102147 SDQLCHi023-A 2021-03-00 2021-03-00 PubMed: 33493992 DOI: 10.1016/j.scr.2020.102147Associated cell lines:
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Abdelalim EM
Modeling different types of diabetes using human pluripotent stem cells
Abdelalim EM. Modeling different types of diabetes using human pluripotent stem cells. . 2021-03-00. Pubmed ID: 33242105; DOI: 10.1007/s00018-020-03710-9; PMC: PMC11072720 QBRIi007-A 2021-03-00 2021-03-00 PubMed: 33242105 DOI: 10.1007/s00018-020-03710-9Associated cell lines:
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Vitale MR, Zöller JEM, Jansch C, Janz A, Edenhofer F, Klopocki E, van den Hove D, Vanmierlo T, Rivero O, Nadif Kasri N, Ziegler GC, Lesch KP
Generation of induced pluripotent stem cell (iPSC) lines carrying a heterozygous (UKWMPi002-A-1) and null mutant knockout (UKWMPi002-A-2) of Cadherin 13 associated with neurodevelopmental disorders using CRISPR/Cas9
Vitale MR et al. Generation of induced pluripotent stem cell (iPSC) lines carrying a heterozygous (UKWMPi002-A-1) and null mutant knockout (UKWMPi002-A-2) of Cadherin 13 associated with neurodevelopmental disorders using CRISPR/Cas9. . 2021-03-00. Pubmed ID: 33486346; DOI: 10.1016/j.scr.2021.102169 UKWMPi002-AUKWMPi002-A-1UKWMPi002-A-2 2021-03-00 2021-03-00 PubMed: 33486346 DOI: 10.1016/j.scr.2021.102169Associated cell lines:
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Liu Y, Li X, Fu W, Liu M, Wang M, Hu L, Wang L, Zhao X, Ding Z, Dong J
An induced pluripotent stem cells line (ZZUNEUi022-A) derived from urine cells of healthy male human
Liu Y et al. An induced pluripotent stem cells line (ZZUNEUi022-A) derived from urine cells of healthy male human. . 2021-03-00. Pubmed ID: 33529980; DOI: 10.1016/j.scr.2021.102191 ZZUNEUi007-AZZUNEUi022-A 2021-03-00 2021-03-00 PubMed: 33529980 DOI: 10.1016/j.scr.2021.102191Associated cell lines:
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Li J, Shang S, Wang T, Fu B, Wang P, Cai G, Chen X, Li Q
Generation of iPSC from peripheral blood mononuclear cells obtained from a patient with TSC2-PKD1 contiguous gene deletion syndrome
Li J et al. Generation of iPSC from peripheral blood mononuclear cells obtained from a patient with TSC2-PKD1 contiguous gene deletion syndrome. . 2021-03-00. Pubmed ID: 33485185; DOI: 10.1016/j.scr.2021.102181 PUMCHi004-A 2021-03-00 2021-03-00 PubMed: 33485185 DOI: 10.1016/j.scr.2021.102181Associated cell lines:
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Yang X, Liu N, Mu H, Lv Y, Zhang H, Li Y, Guan J, Gai Z, Liu Y
Reprogramming of human peripheral blood mononuclear cell (PBMC) from a patient suffering from hearing loss into iPSC line (SDQLCHi035-A) maintaining compound heterozygous variations in GJB2 gene
Yang X et al. Reprogramming of human peripheral blood mononuclear cell (PBMC) from a patient suffering from hearing loss into iPSC line (SDQLCHi035-A) maintaining compound heterozygous variations in GJB2 gene. . 2021-03-00. Pubmed ID: 33517119; DOI: 10.1016/j.scr.2021.102188 SDQLCHi035-A 2021-03-00 2021-03-00 PubMed: 33517119 DOI: 10.1016/j.scr.2021.102188Associated cell lines:
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Cui S, Shin YJ, Ko EJ, Lim SW, Ju JH, Lee KI, Lee JY, Yang CW, Chung BH
Human-induced pluripotent stem cell lines (CMCi006-A and CMCi007-A) from a female and male patient with Fabry disease carrying the same frameshift deletion mutation
Cui S et al. Human-induced pluripotent stem cell lines (CMCi006-A and CMCi007-A) from a female and male patient with Fabry disease carrying the same frameshift deletion mutation. . 2021-03-00. Pubmed ID: 33545641; DOI: 10.1016/j.scr.2021.102214 CMCi006-ACMCi007-A 2021-03-00 2021-03-00 PubMed: 33545641 DOI: 10.1016/j.scr.2021.102214 -
Meng-Jie L.
Application progress of induced pluripotent stem cells in Alzheimer's disease
Meng-Jie L.. Application progress of induced pluripotent stem cells in Alzheimer's disease. . 2021-02-28. DOI: 10.11855/j.issn.0577-7402.2021.02.14 IMEDEAi006-A 2021-02-28 2021-02-28 DOI: 10.11855/j.issn.0577-7402.2021.02.14Associated cell lines:
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Schnichels S, Paquet-Durand F, Löscher M, Tsai T, Hurst J, Joachim SC, Klettner A
Retina in a dish: Cell cultures, retinal explants and animal models for common diseases of the retina
Schnichels S et al. Retina in a dish: Cell cultures, retinal explants and animal models for common diseases of the retina. . 2021-03-00. Pubmed ID: 32721458; DOI: 10.1016/j.preteyeres.2020.100880 CABi003-A 2021-03-00 2021-03-00 PubMed: 32721458 DOI: 10.1016/j.preteyeres.2020.100880Associated cell lines:
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Kim J, Koh H, Zhen X, Lee DS, Ha HY, Lee JH
Establishment of iPSC (KRIBBi001-A) from CD34(+) group O D-negative bone marrow blood
Kim J et al. Establishment of iPSC (KRIBBi001-A) from CD34(+) group O D-negative bone marrow blood. . 2021-03-00. Pubmed ID: 33529979; DOI: 10.1016/j.scr.2021.102199 KRIBBi001-A 2021-03-00 2021-03-00 PubMed: 33529979 DOI: 10.1016/j.scr.2021.102199Associated cell lines:
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Wang B, Yang L, Li Y, Gao M, Zhang H, Yang X, Guan J, Liu Y, Gai Z
Establishment of a human induced pluripotent stem cell line (SDQLCHi037-A) from a patient with Alagille syndrome carrying heterozygous mutation in JAG1 gene
Wang B et al. Establishment of a human induced pluripotent stem cell line (SDQLCHi037-A) from a patient with Alagille syndrome carrying heterozygous mutation in JAG1 gene. . 2021-03-00. Pubmed ID: 33465531; DOI: 10.1016/j.scr.2021.102162 SDQLCHi037-A 2021-03-00 2021-03-00 PubMed: 33465531 DOI: 10.1016/j.scr.2021.102162Associated cell lines:
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Sahabian A, Dahlmann J, Martin U, Olmer R
Production and cryopreservation of definitive endoderm from human pluripotent stem cells under defined and scalable culture conditions
Sahabian A et al. Production and cryopreservation of definitive endoderm from human pluripotent stem cells under defined and scalable culture conditions. . 2021-03-00. Pubmed ID: 33580232; DOI: 10.1038/s41596-020-00470-5 MHHi006-AMHHi006-A-4 2021-03-00 2021-03-00 PubMed: 33580232 DOI: 10.1038/s41596-020-00470-5Associated cell lines:
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Fan L, Mao C, Shi C, Fan Y, Liu F, Zheng H, Su Y, Liu H, Wang Y, Liu YT, Yang J, Xu Y
Generation of an induced pluripotent stem cell line (ZZUi022-A) from a paroxysmal kinesigenic dyskinesia individual carrying the PRRT2 gene mutation
Fan L et al. Generation of an induced pluripotent stem cell line (ZZUi022-A) from a paroxysmal kinesigenic dyskinesia individual carrying the PRRT2 gene mutation. . 2021-03-00. Pubmed ID: 33550051; DOI: 10.1016/j.scr.2021.102210 ZZUi022-AZZUi037-A 2021-03-00 2021-03-00 PubMed: 33550051 DOI: 10.1016/j.scr.2021.102210 -
Chen H, Ding Y, Zhou W, Li J, Qian W, Zhang Z, Li C, Tong H, Rong X, Chu M, Chen C, Wang D, Guo X
Establishment of an induced pluripotent stem cell line (WMUi016-A) from a patient with X-linked Dent disease (X-Dent) carrying the hemizygote mutation p.R718* (c.2152C > T) in the CLCN5 gene
Chen H et al. Establishment of an induced pluripotent stem cell line (WMUi016-A) from a patient with X-linked Dent disease (X-Dent) carrying the hemizygote mutation p.R718* (c.2152C > T) in the CLCN5 gene. . 2021-03-00. Pubmed ID: 33545640; DOI: 10.1016/j.scr.2021.102209 WMUi016-A 2021-03-00 2021-03-00 PubMed: 33545640 DOI: 10.1016/j.scr.2021.102209Associated cell lines:
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Chen M, Lin SM, Li N, Li Y, Li Y, Zhang L
An induced pluripotent stem cell line (GZHMCi003-A) derived from a fetus with exon 3 heterozygous deletion in RUNX2 gene causing cleidocranial dysplasia
Chen M et al. An induced pluripotent stem cell line (GZHMCi003-A) derived from a fetus with exon 3 heterozygous deletion in RUNX2 gene causing cleidocranial dysplasia. . 2021-03-00. Pubmed ID: 33477036; DOI: 10.1016/j.scr.2021.102166 GZHMCi003-A 2021-03-00 2021-03-00 PubMed: 33477036 DOI: 10.1016/j.scr.2021.102166Associated cell lines:
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Zhang W, Hua Y, Di W, Guo J, Dai Q, Zhao J, Zhang B, Wang Y
Generation of a human induced pluripotent stem cell line (SIAISi011-A) from a 61-year-old Chinese Han healthy female donor
Zhang W et al. Generation of a human induced pluripotent stem cell line (SIAISi011-A) from a 61-year-old Chinese Han healthy female donor. . 2021-03-00. Pubmed ID: 33465532; DOI: 10.1016/j.scr.2021.102173 SIAISi011-A 2021-03-00 2021-03-00 PubMed: 33465532 DOI: 10.1016/j.scr.2021.102173Associated cell lines:
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Zehravi M, Wahid M, Ashraf J
Episomal reprogramming of Duchenne muscular dystrophy patients derived CD3(+) T cells towards induced pluripotent stem cells
Zehravi M et al. Episomal reprogramming of Duchenne muscular dystrophy patients derived CD3(+) T cells towards induced pluripotent stem cells. . 2021-03-00. Pubmed ID: 33679927; DOI: 10.12669/pjms.37.2.3388; PMC: PMC7931302 MUSIi011-AMUSIi011-B 2021-03-00 2021-03-00 PubMed: 33679927 DOI: 10.12669/pjms.37.2.3388Associated cell lines:
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Liu X, Liu Y, Ma Y, Gong Y, Liu Q, Sun W, Guo H
Establishment of patient-specific induced pluripotent stem cell line SDUBMSi009-A from a patient with X-linked Lowe syndrome
Liu X et al. Establishment of patient-specific induced pluripotent stem cell line SDUBMSi009-A from a patient with X-linked Lowe syndrome. . 2021-03-00. Pubmed ID: 33540283; DOI: 10.1016/j.scr.2021.102171 SDUBMSi009-A 2021-03-00 2021-03-00 PubMed: 33540283 DOI: 10.1016/j.scr.2021.102171Associated cell lines:
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Dong W, Shi D, Zhang L, Huang M, Luo Q
Generation of an induced pluripotent stem cell line ZZUNEUi019-A from a five-year-old Chinese girl with Susceptibility to idiopathic generalized epilepsy-15
Dong W et al. Generation of an induced pluripotent stem cell line ZZUNEUi019-A from a five-year-old Chinese girl with Susceptibility to idiopathic generalized epilepsy-15. . 2021-03-00. Pubmed ID: 33540281; DOI: 10.1016/j.scr.2021.102177 SHCDNi001-AZZUNEUi019-A 2021-03-00 2021-03-00 PubMed: 33540281 DOI: 10.1016/j.scr.2021.102177Associated cell lines:
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He L, Chen Z, Peng L, Tang B, Jiang H
Human stem cell models of polyglutamine diseases: Sources for disease models and cell therapy
He L et al. Human stem cell models of polyglutamine diseases: Sources for disease models and cell therapy. . 2021-03-00. Pubmed ID: 33347831; DOI: 10.1016/j.expneurol.2020.113573 ZZUi004-ALUMCi002-ALUMCi003-AMUSIi004-AHIHCNi002-AICGi007-ALUMCi007-ALUMCi008-AIBCHi001-ACSSi008-ACSUXHi001-ACSUXHi002-A 2021-03-00 2021-03-00 PubMed: 33347831 DOI: 10.1016/j.expneurol.2020.113573Associated cell lines:
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Hanss Z, Larsen SB, Antony P, Mencke P, Massart F, Jarazo J, Schwamborn JC, Barbuti PA, Mellick GD, Krüger R
Mitochondrial and Clearance Impairment in p.D620N VPS35 Patient-Derived Neurons
Hanss Z et al. Mitochondrial and Clearance Impairment in p.D620N VPS35 Patient-Derived Neurons. . 2021-03-00. Pubmed ID: 33142012; DOI: 10.1002/mds.28365; PMC: PMC8048506 LCSBi001-A 2021-03-00 2021-03-00 PubMed: 33142012 DOI: 10.1002/mds.28365Associated cell lines:
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Xu M, Wang L, Yin J, Xiong J, Guo Q, Yang W
Establishment of an induced pluripotent stem cell line (SAHGMUi001-A) from a patient with Netherton syndrome carrying SPINK5 mutation
Xu M et al. Establishment of an induced pluripotent stem cell line (SAHGMUi001-A) from a patient with Netherton syndrome carrying SPINK5 mutation. . 2021-03-00. Pubmed ID: 33556917; DOI: 10.1016/j.scr.2021.102213 SAHGMUi001-A 2021-03-00 2021-03-00 PubMed: 33556917 DOI: 10.1016/j.scr.2021.102213Associated cell lines:
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Kamand M, Forsberg SL, Thomassen M, Ilieva M, Meyer M, Svenningsen ÅF, Michel TM
Establishment of an induced pluripotent stem (iPS) cell line (SDUKIi006-A) from a 21-year old male patient diagnosed with atypical autism disorder
Kamand M et al. Establishment of an induced pluripotent stem (iPS) cell line (SDUKIi006-A) from a 21-year old male patient diagnosed with atypical autism disorder. . 2021-03-00. Pubmed ID: 33524673; DOI: 10.1016/j.scr.2021.102185 SDUKIi002-ASDUKIi006-A 2021-03-00 2021-03-00 PubMed: 33524673 DOI: 10.1016/j.scr.2021.102185Associated cell lines:
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Hathy E, Szabó E, Vincze K, Haltrich I, Kiss E, Varga N, Erdei Z, Várady G, Homolya L, Apáti Á, Réthelyi JM
Generation of multiple iPSC clones from a male schizophrenia patient carrying de novo mutations in genes KHSRP, LRRC7, and KIR2DL1, and his parents
Hathy E et al. Generation of multiple iPSC clones from a male schizophrenia patient carrying de novo mutations in genes KHSRP, LRRC7, and KIR2DL1, and his parents. . 2021-03-00. Pubmed ID: 33503521; DOI: 10.1016/j.scr.2020.102140 SUi001-ASUi002-ASUi003-A 2021-03-00 2021-03-00 PubMed: 33503521 DOI: 10.1016/j.scr.2020.102140 -
Bono F, Mutti V, Piovani G, Minelli A, Mingardi J, Guglielmi A, Missale C, Gennarelli M, Fiorentini C, Barbon A
Establishment and characterization of induced pluripotent stem cell (iPSCs) line UNIBSi014-A from a healthy female donor
Bono F et al. Establishment and characterization of induced pluripotent stem cell (iPSCs) line UNIBSi014-A from a healthy female donor. . 2021-03-00. Pubmed ID: 33548809; DOI: 10.1016/j.scr.2021.102216 UNIBSi012-AUNIBSi013-AUNIBSi014-A 2021-03-00 2021-03-00 PubMed: 33548809 DOI: 10.1016/j.scr.2021.102216Associated cell lines:
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Zhang H, Zhang H, Ma Y, Lv Y, Gai Z, Liu Y
Generation and characterization of an induced pluripotent stem cell line SDQLCHi018-A from a congenital myasthenic syndrome patient carrying compound heterozygote mutations in RAPSN gene
Zhang H et al. Generation and characterization of an induced pluripotent stem cell line SDQLCHi018-A from a congenital myasthenic syndrome patient carrying compound heterozygote mutations in RAPSN gene. . 2021-03-00. Pubmed ID: 33465529; DOI: 10.1016/j.scr.2021.102160 SDQLCHi018-A 2021-03-00 2021-03-00 PubMed: 33465529 DOI: 10.1016/j.scr.2021.102160Associated cell lines:
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Dong T, Zhang S, Chang Y, Bai R, Jiang Y, Ma S, Li Y, Jiang HF, Lu WJ
The establishment of a homozygous SNTA1 knockout human embryonic stem cell line (WAe009-A-50) using the CRISPR/Cas9 system
Dong T et al. The establishment of a homozygous SNTA1 knockout human embryonic stem cell line (WAe009-A-50) using the CRISPR/Cas9 system. . 2021-03-00. Pubmed ID: 33524674; DOI: 10.1016/j.scr.2021.102196 WAe009-AWAe009-A-50 2021-03-00 2021-03-00 PubMed: 33524674 DOI: 10.1016/j.scr.2021.102196Associated cell lines:
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Ko EJ, Cui S, Shin YJ, Lim SW, Lee KI, Lee JY, Yang CW, Kim M, Chung BH
Generation of the human induced pluripotent stem cell lines (CMCi009-A) from a patient with Birt-Hogg-Dubé syndrome (BHD) with heterozygous frameshift deletion mutation c.1285delC of the FLCN gene
Ko EJ et al. Generation of the human induced pluripotent stem cell lines (CMCi009-A) from a patient with Birt-Hogg-Dubé syndrome (BHD) with heterozygous frameshift deletion mutation c.1285delC of the FLCN gene. . 2021-03-00. Pubmed ID: 33540282; DOI: 10.1016/j.scr.2021.102215 CMCi009-A 2021-03-00 2021-03-00 PubMed: 33540282 DOI: 10.1016/j.scr.2021.102215Associated cell lines:
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Liu N, Yang X, Wang S, Dong R, Li Y, Lv Y, Liu Y, Gai Z
PBMC-derived integration-free iPSCs line SDQLCHi039-A from a patient with X-linked agammaglobulinemia carrying a novel 9-bp in-frame deletion in BTK gene
Liu N et al. PBMC-derived integration-free iPSCs line SDQLCHi039-A from a patient with X-linked agammaglobulinemia carrying a novel 9-bp in-frame deletion in BTK gene. . 2021-03-00. Pubmed ID: 33453577; DOI: 10.1016/j.scr.2021.102165 SDQLCHi039-A 2021-03-00 2021-03-00 PubMed: 33453577 DOI: 10.1016/j.scr.2021.102165Associated cell lines:
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Inzunza J, Arias-Fuenzalida J, Segura-Aguilar J, Nalvarte I, Varshney M
Generation of nonviral integration-free human iPS cell line KISCOi001-A from normal human fibroblasts, under defined xeno-free and feeder-free conditions
Inzunza J et al. Generation of nonviral integration-free human iPS cell line KISCOi001-A from normal human fibroblasts, under defined xeno-free and feeder-free conditions. . 2021-03-00. Pubmed ID: 33517122; DOI: 10.1016/j.scr.2021.102193 KISCOi001-A 2021-03-00 2021-03-00 PubMed: 33517122 DOI: 10.1016/j.scr.2021.102193Associated cell lines:
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Li X, Fu W, Guo G, Liu M, Du W, Zhao J, Liu Y, Wang L, Dong J, Zhao X
A heterozygous MYH7 (c. 2156G > A) mutant human induced pluripotent stem cell line (ZZUNEUi020-A) generated from a patient with hypertrophic cardiomyopathy
Li X et al. A heterozygous MYH7 (c. 2156G > A) mutant human induced pluripotent stem cell line (ZZUNEUi020-A) generated from a patient with hypertrophic cardiomyopathy. . 2021-03-00. Pubmed ID: 33453578; DOI: 10.1016/j.scr.2021.102158 ZZUNEUi020-A 2021-03-00 2021-03-00 PubMed: 33453578 DOI: 10.1016/j.scr.2021.102158Associated cell lines:
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Zhang X, Zhang D, Thompson JA, Chen SC, Huang Z, Jennings L, McLaren TL, Lamey TM, De Roach JN, Chen FK, McLenachan S
Gene correction of the CLN3 c.175G>A variant in patient-derived induced pluripotent stem cells prevents pathological changes in retinal organoids
Zhang X et al. Gene correction of the CLN3 c.175G>A variant in patient-derived induced pluripotent stem cells prevents pathological changes in retinal organoids. . 2021-03-00. Pubmed ID: 33497524; DOI: 10.1002/mgg3.1601; PMC: PMC8104174 LEIi004-ALEIi004-A-1 2021-03-00 2021-03-00 PubMed: 33497524 DOI: 10.1002/mgg3.1601Associated cell lines:
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Zhang D, McLenachan S, Chen SC, Zaw K, Alziyadat Y, Zhang X, Lamey TM, Thompson JA, McLaren TL, Mellough C, De Roach JN, Chen FK
Generation of two induced pluripotent stem cell lines from a patient with recessive inherited retinal disease caused by compound heterozygous mutations in SNRNP200
Zhang D et al. Generation of two induced pluripotent stem cell lines from a patient with recessive inherited retinal disease caused by compound heterozygous mutations in SNRNP200. . 2021-03-00. Pubmed ID: 33429167; DOI: 10.1016/j.scr.2020.102154 LEIi015-ALEIi015-B 2021-03-00 2021-03-00 PubMed: 33429167 DOI: 10.1016/j.scr.2020.102154 -
Graffmann N, Martins S, Ljubikj T, Matte JC, Bohndorf M, Wruck W, Adjaye J
Generation of a Crigler-Najjar Syndrome Type I patient-derived induced pluripotent stem cell line CNS705 (HHUUKDi005-A)
Graffmann N et al. Generation of a Crigler-Najjar Syndrome Type I patient-derived induced pluripotent stem cell line CNS705 (HHUUKDi005-A). . 2021-03-00. Pubmed ID: 33485181; DOI: 10.1016/j.scr.2021.102167 HHUUKDi005-A 2021-03-00 2021-03-00 PubMed: 33485181 DOI: 10.1016/j.scr.2021.102167Associated cell lines:
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Qin Z, Sun L, Sun X, Gao X, Su H
Reprogramming of a human induced pluripotent stem cell line from a Marfan syndrome patient harboring a heterozygous mutation of c.2939G > A in FBN1 gene
Qin Z et al. Reprogramming of a human induced pluripotent stem cell line from a Marfan syndrome patient harboring a heterozygous mutation of c.2939G > A in FBN1 gene. . 2021-03-00. Pubmed ID: 33450697; DOI: 10.1016/j.scr.2021.102163 ZZUSAHi003-A 2021-03-00 2021-03-00 PubMed: 33450697 DOI: 10.1016/j.scr.2021.102163Associated cell lines:
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Yang Z, Yuan F, Wang N, Liu Y, Zhang J, Wei R, Wu F, Wu Y, You K, Chen Y, Yang F, Li YX
Generation of a DKK1 homozygous knockout human embryonic stem cell line WAe001-A-21 using CRISPR/Cas9
Yang Z et al. Generation of a DKK1 homozygous knockout human embryonic stem cell line WAe001-A-21 using CRISPR/Cas9. . 2021-03-00. Pubmed ID: 33461039; DOI: 10.1016/j.scr.2021.102161 WAe001-AWAe001-A-21 2021-03-00 2021-03-00 PubMed: 33461039 DOI: 10.1016/j.scr.2021.102161Associated cell lines:
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Karthik R, Menaka R, Hariharan M, Won D
Ischemic Lesion Segmentation using Ensemble of Multi-Scale Region Aligned CNN
Karthik R et al. Ischemic Lesion Segmentation using Ensemble of Multi-Scale Region Aligned CNN. . 2021-03-00. Pubmed ID: 33223277; DOI: 10.1016/j.cmpb.2020.105831 ZJUi005-A 2021-03-00 2021-03-00 PubMed: 33223277 DOI: 10.1016/j.cmpb.2020.105831Associated cell lines:
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Pandolfi EC, Sosa E, Hunt TJ, Goldsmith S, Hurlbut K, Silber SJ, Clark AT
Generation of six human induced pluripotent stem cell sublines (MZT01E, MZT01F, MZT01N and MZT02D, MZT02G and MZT02H) for reproductive science research
Pandolfi EC et al. Generation of six human induced pluripotent stem cell sublines (MZT01E, MZT01F, MZT01N and MZT02D, MZT02G and MZT02H) for reproductive science research. . 2021-03-00. Pubmed ID: 33548810; DOI: 10.1016/j.scr.2021.102204; PMC: PMC8043044 UCLAi002-AUCLAi002-BUCLAi002-CUCLAi003-AUCLAi003-BUCLAi003-C 2021-03-00 2021-03-00 PubMed: 33548810 DOI: 10.1016/j.scr.2021.102204Associated cell lines:
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Zhao T, Bai R, Wu F, Lu WJ, Zhang J
Generation of a TBX5 homozygous knockout embryonic stem cell line (WAe009-A-45) by CRISPR/Cas9 genome editing
Zhao T et al. Generation of a TBX5 homozygous knockout embryonic stem cell line (WAe009-A-45) by CRISPR/Cas9 genome editing. . 2021-03-00. Pubmed ID: 33497883; DOI: 10.1016/j.scr.2021.102156 WAe009-AWAe009-A-45 2021-03-00 2021-03-00 PubMed: 33497883 DOI: 10.1016/j.scr.2021.102156Associated cell lines:
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Wen J, Song J, He C, Ling J, Liu Y, Chen H, Gong W, Mei L, Feng Y
Establishment of an iPSC line (CSUXHi003-A) from a patient with Waardenburg syndrome type Ⅱ caused by a MITF mutation
Wen J et al. Establishment of an iPSC line (CSUXHi003-A) from a patient with Waardenburg syndrome type Ⅱ caused by a MITF mutation. . 2021-03-00. Pubmed ID: 33454628; DOI: 10.1016/j.scr.2021.102157 JTUi002-ACSUXHi003-A 2021-03-00 2021-03-00 PubMed: 33454628 DOI: 10.1016/j.scr.2021.102157Associated cell lines:
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Harding P, Lima Cunha D, Méjécase C, Eintracht J, Toualbi L, Sarkar H, Moosajee M
Generation of human iPSC line (UCLi013-A) from a patient with microphthalmia and aniridia, carrying a heterozygous missense mutation c.372C>A p.(Asn124Lys) in PAX6
Harding P et al. Generation of human iPSC line (UCLi013-A) from a patient with microphthalmia and aniridia, carrying a heterozygous missense mutation c.372C>A p.(Asn124Lys) in PAX6. . 2021-03-00. Pubmed ID: 33524672; DOI: 10.1016/j.scr.2021.102184; PMC: PMC7957338 UCLi013-A 2021-03-00 2021-03-00 PubMed: 33524672 DOI: 10.1016/j.scr.2021.102184Associated cell lines:
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Hou C, Xie L, Qiu Q, Lin H, Liu W, Sun X, Zhang Y, Xu M, Li Y, Xiao T
Generation of an induced pluripotent stem cell line from a Chinese Han infant with floating-harbor syndrome accompanied with dilated cardiomyopathy
Hou C et al. Generation of an induced pluripotent stem cell line from a Chinese Han infant with floating-harbor syndrome accompanied with dilated cardiomyopathy. . 2021-03-00. Pubmed ID: 33517121; DOI: 10.1016/j.scr.2021.102182 SHETi001-A 2021-03-00 2021-03-00 PubMed: 33517121 DOI: 10.1016/j.scr.2021.102182Associated cell lines:
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Wang L, Gao B, Mo X, Guo X, Huang J
Generation of an urine-derived induced pluripotent stem cell line from a 6-year old X-linked adrenoleukodystrophy (X-ALD) patient
Wang L et al. Generation of an urine-derived induced pluripotent stem cell line from a 6-year old X-linked adrenoleukodystrophy (X-ALD) patient. . 2021-03-00. Pubmed ID: 33472124; DOI: 10.1016/j.scr.2021.102170 WMUi014-A 2021-03-00 2021-03-00 PubMed: 33472124 DOI: 10.1016/j.scr.2021.102170Associated cell lines:
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Guo X, Zhang X, Wang L, He L, Ding Y, Chen H, Wang D, Rong X, Shen X, Lin J, Chu M
Generation of an urine-derived induced pluripotent stem cell line WMUi017-A from a X-linked Renpenning syndrome (X-RSY) patient with the hemizygous PQBP1 gene mutation p.P609A (c.1825C>G)
Guo X et al. Generation of an urine-derived induced pluripotent stem cell line WMUi017-A from a X-linked Renpenning syndrome (X-RSY) patient with the hemizygous PQBP1 gene mutation p.P609A (c.1825C>G). . 2021-03-00. Pubmed ID: 33477035; DOI: 10.1016/j.scr.2021.102159 WMUi017-A 2021-03-00 2021-03-00 PubMed: 33477035 DOI: 10.1016/j.scr.2021.102159Associated cell lines:
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Hou C, Liu W, Xie L, Zheng J, Chen X, Sun X, Zhang Y, Xu M, Li Y, Xiao T
Generation of an induced pluripotent stem cell line from a Chinese Han child with arrhythmia
Hou C et al. Generation of an induced pluripotent stem cell line from a Chinese Han child with arrhythmia. . 2021-03-00. Pubmed ID: 33497884; DOI: 10.1016/j.scr.2021.102183 SHETi002-A 2021-03-00 2021-03-00 PubMed: 33497884 DOI: 10.1016/j.scr.2021.102183Associated cell lines:
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Chen ZT, Zhao ZH, Chen LN, Fan F, Cai GE, Weng HD, Wang YQ, Liao LM, Chen XC, Huang E, Ye QY
Generation of an induced pluripotent stem cell line, FJMUUHi001-A, from a hereditary Parkinson's disease patient with homozygous mutation of c.189dupA in PARK7
Chen ZT et al. Generation of an induced pluripotent stem cell line, FJMUUHi001-A, from a hereditary Parkinson's disease patient with homozygous mutation of c.189dupA in PARK7. . 2021-03-00. Pubmed ID: 33485186; DOI: 10.1016/j.scr.2021.102175 FJMUUHi001-A 2021-03-00 2021-03-00 PubMed: 33485186 DOI: 10.1016/j.scr.2021.102175Associated cell lines:
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Li D, Hong X, Li W, Meng S, Yu H, Zhang X, Wang C, Samokhvalov IM, Liu D, Tang D, Dai Y
Establishment of an induced pluripotent stem cell line SPHi001-A from a systemic lupus erythematosus patient combined with preeclampsia and psoriasis
Li D et al. Establishment of an induced pluripotent stem cell line SPHi001-A from a systemic lupus erythematosus patient combined with preeclampsia and psoriasis. . 2021-03-00. Pubmed ID: 33516123; DOI: 10.1016/j.scr.2021.102192 SPHi001-A 2021-03-00 2021-03-00 PubMed: 33516123 DOI: 10.1016/j.scr.2021.102192Associated cell lines:
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Lam CK, Wu JC
Clinical Trial in a Dish: Using Patient-Derived Induced Pluripotent Stem Cells to Identify Risks of Drug-Induced Cardiotoxicity
Lam CK et al. Clinical Trial in a Dish: Using Patient-Derived Induced Pluripotent Stem Cells to Identify Risks of Drug-Induced Cardiotoxicity. . 2021-03-00. Pubmed ID: 33472401; DOI: 10.1161/atvbaha.120.314695; PMC: PMC11006431 NUIGi005-ANUIGi005-BNUIGi005-CNUIGi006-ANUIGi006-BNUIGi006-CNUIGi007-ANUIGi007-B 2021-03-00 2021-03-00 PubMed: 33472401 DOI: 10.1161/atvbaha.120.314695Associated cell lines:
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Appelt PA, Comella K, de Souza LAPS, Luvizutto GJ
Effect of stem cell treatment on functional recovery of spinocerebellar ataxia: systematic review and meta-analysis
Appelt PA et al. Effect of stem cell treatment on functional recovery of spinocerebellar ataxia: systematic review and meta-analysis. . 2021-02-25. Pubmed ID: 33632326; DOI: 10.1186/s40673-021-00130-8; PMC: PMC7905903 CHOPi002-ACHOPi003-A 2021-02-25 2021-02-25 PubMed: 33632326 DOI: 10.1186/s40673-021-00130-8Associated cell lines:
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Goh KJ, Tan EK, Lu H, Roy S, Dunn NR
An NKX2-1(GFP) and TP63(tdTomato) dual fluorescent reporter for the investigation of human lung basal cell biology
Goh KJ et al. An NKX2-1(GFP) and TP63(tdTomato) dual fluorescent reporter for the investigation of human lung basal cell biology. . 2021-02-25. Pubmed ID: 33633173; DOI: 10.1038/s41598-021-83825-6; PMC: PMC7907081 MHHi002-AMHHi006-AMHHi002-A-2MHHi006-A-2MHHi006-A-4 2021-02-25 2021-02-25 PubMed: 33633173 DOI: 10.1038/s41598-021-83825-6Associated cell lines:
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Witte A, Rohlfing AK, Dannenmann B, Dicenta V, Nasri M, Kolb K, Sudmann J, Castor T, Rath D, Borst O, Skokowa J, Gawaz M
The chemokine CXCL14 mediates platelet function and migration via direct interaction with CXCR4
Witte A et al. The chemokine CXCL14 mediates platelet function and migration via direct interaction with CXCR4. . 2021-02-22. Pubmed ID: 32239134; DOI: 10.1093/cvr/cvaa080 MHHi015-A 2021-02-22 2021-02-22 PubMed: 32239134 DOI: 10.1093/cvr/cvaa080Associated cell lines:
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Nikitina TV, Kashevarova AA, Gridina MM, Lopatkina ME, Khabarova AA, Yakovleva YS, Menzorov AG, Minina YA, Pristyazhnyuk IE, Vasilyev SA, Fedotov DA, Serov OL, Lebedev IN
Complex biology of constitutional ring chromosomes structure and (in)stability revealed by somatic cell reprogramming
Nikitina TV et al. Complex biology of constitutional ring chromosomes structure and (in)stability revealed by somatic cell reprogramming. . 2021-02-22. Pubmed ID: 33619287; DOI: 10.1038/s41598-021-83399-3; PMC: PMC7900208 IMGTi001-AIMGTi001-BIMGTi003-AICGi024-AICGi025-A 2021-02-22 2021-02-22 PubMed: 33619287 DOI: 10.1038/s41598-021-83399-3Associated cell lines:
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Ho R, Workman MJ, Mathkar P, Wu K, Kim KJ, O'Rourke JG, Kellogg M, Montel V, Banuelos MG, Arogundade OA, Diaz-Garcia S, Oheb D, Huang S, Khrebtukova I, Watson L, Ravits J, Taylor K, Baloh RH, Svendsen CN
Cross-Comparison of Human iPSC Motor Neuron Models of Familial and Sporadic ALS Reveals Early and Convergent Transcriptomic Disease Signatures
Ho R et al. Cross-Comparison of Human iPSC Motor Neuron Models of Familial and Sporadic ALS Reveals Early and Convergent Transcriptomic Disease Signatures. . 2021-02-17. Pubmed ID: 33382996; DOI: 10.1016/j.cels.2020.10.010; PMC: PMC7897311 EDi034-A 2021-02-17 2021-02-17 PubMed: 33382996 DOI: 10.1016/j.cels.2020.10.010Associated cell lines:
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Lima Cunha D, Oram A, Gruber R, Plank R, Lingenhel A, Gupta MK, Altmüller J, Nürnberg P, Schmuth M, Zschocke J, Šarić T, Eckl KM, Hennies HC
hiPSC-Derived Epidermal Keratinocytes from Ichthyosis Patients Show Altered Expression of Cornification Markers
Lima Cunha D et al. hiPSC-Derived Epidermal Keratinocytes from Ichthyosis Patients Show Altered Expression of Cornification Markers. . 2021-02-11. Pubmed ID: 33670118; DOI: 10.3390/ijms22041785; PMC: PMC7916893 UCLi016-AUCLi017-A 2021-02-11 2021-02-11 PubMed: 33670118 DOI: 10.3390/ijms22041785 -
Wang L, Sievert D, Clark AE, Federman H, Gastfriend BD, Shusta E, Palecek SP, Carlin AF, Gleeson J
A Human 3D neural assembloid model for SARS-CoV-2 infection
Wang L et al. A Human 3D neural assembloid model for SARS-CoV-2 infection. . 2021-02-09. Pubmed ID: 33594369; DOI: 10.1101/2021.02.09.430349; PMC: PMC7885921 WAe001-A 2021-02-09 2021-02-09 PubMed: 33594369 DOI: 10.1101/2021.02.09.430349Associated cell lines:
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Li Q, Sun Y, van IJzendoorn SCD
A Link between Intrahepatic Cholestasis and Genetic Variations in Intracellular Trafficking Regulators
Li Q et al. A Link between Intrahepatic Cholestasis and Genetic Variations in Intracellular Trafficking Regulators. . 2021-02-04. Pubmed ID: 33557414; DOI: 10.3390/biology10020119; PMC: PMC7914782 DHMCi005-A 2021-02-04 2021-02-04 PubMed: 33557414 DOI: 10.3390/biology10020119Associated cell lines:
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Rim YA, Nam Y, Park N, Lee K, Jung H, Jung SM, Lee J, Ju JH
Characterization of Early-Onset Finger Osteoarthritis-Like Condition Using Patient-Derived Induced Pluripotent Stem Cells
Rim YA et al. Characterization of Early-Onset Finger Osteoarthritis-Like Condition Using Patient-Derived Induced Pluripotent Stem Cells. . 2021-02-04. Pubmed ID: 33557199; DOI: 10.3390/cells10020317; PMC: PMC7913990 BRCi001-A 2021-02-04 2021-02-04 PubMed: 33557199 DOI: 10.3390/cells10020317Associated cell lines:
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Saito MK
Elucidation of the Pathogenesis of Autoinflammatory Diseases Using iPS Cells
Saito MK. Elucidation of the Pathogenesis of Autoinflammatory Diseases Using iPS Cells. . 2021-02-01. Pubmed ID: 33535645; DOI: 10.3390/children8020094; PMC: PMC7912798 NIHTVBi014-ASDQLCHi012-A 2021-02-01 2021-02-01 PubMed: 33535645 DOI: 10.3390/children8020094Associated cell lines:
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Jansch C, Ziegler GC, Forero A, Gredy S, Wäldchen S, Vitale MR, Svirin E, Zöller JEM, Waider J, Günther K, Edenhofer F, Sauer M, Wischmeyer E, Lesch KP
Serotonin-specific neurons differentiated from human iPSCs form distinct subtypes with synaptic protein assembly
Jansch C et al. Serotonin-specific neurons differentiated from human iPSCs form distinct subtypes with synaptic protein assembly. . 2021-02-00. Pubmed ID: 33560471; DOI: 10.1007/s00702-021-02303-5; PMC: PMC7914246 JMUi001-AUKWMPi001-B 2021-02-00 2021-02-00 PubMed: 33560471 DOI: 10.1007/s00702-021-02303-5Associated cell lines:
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Dobrindt K, Zhang H, Das D, Abdollahi S, Prorok T, Ghosh S, Weintraub S, Genovese G, Powell SK, Lund A, Akbarian S, Eggan K, McCarroll S, Duan J, Avramopoulos D, Brennand KJ
Publicly Available hiPSC Lines with Extreme Polygenic Risk Scores for Modeling Schizophrenia
Dobrindt K et al. Publicly Available hiPSC Lines with Extreme Polygenic Risk Scores for Modeling Schizophrenia. . 2021-02-00. Pubmed ID: 34883504; DOI: 10.1159/000512716; PMC: PMC7923934 CIRMi166-ACIRMi171-ACIRMi173-ACIRMi269-ACIRMi280-ACIRMi372-ACIRMi382-ACIRMi394-ACIRMi407-ACIRMi474-ACIRMi541-ACIRMi596-ACIRMi676-ACIRMi688-ACIRMi817-ACIRMi849-ACIRMi879-ACIRMi946-ACIRMi954-ACIRMi00R-ACIRMi02O-ACIRMi03T-ACIRMi04U-ACIRMi05X-ACIRMi14T-ACIRMi18J-ACIRMi18P-A 2021-02-00 2021-02-00 PubMed: 34883504 DOI: 10.1159/000512716 -
Sinenko SA, Ponomartsev SV, Tomilin AN
Pluripotent stem cell-based gene therapy approach: human de novo synthesized chromosomes
Sinenko SA et al. Pluripotent stem cell-based gene therapy approach: human de novo synthesized chromosomes. . 2021-02-00. Pubmed ID: 33011821; DOI: 10.1007/s00018-020-03653-1; PMC: PMC11072874 FAMRCi007-AFAMRCi007-B 2021-02-00 2021-02-00 PubMed: 33011821 DOI: 10.1007/s00018-020-03653-1Associated cell lines:
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Zhu K, Ma W, Li J, Zhang YS, Zhang W, Lai H, Wang C
Modeling aortic diseases using induced pluripotent stem cells
Zhu K et al. Modeling aortic diseases using induced pluripotent stem cells. . 2021-02-00. Pubmed ID: 33179450; DOI: 10.1002/sctm.20-0322; PMC: PMC7848399 ISMMSi002-BMHHi012-AMHHi013-AMHHi014-A 2021-02-00 2021-02-00 PubMed: 33179450 DOI: 10.1002/sctm.20-0322Associated cell lines:
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Bose B
Induced Pluripotent Stem Cells (iPSCs) Derived 3D Human Lung Organoids from Different Ethnicities to Understand the SARS-CoV2 Severity/Infectivity Percentage
Bose B. Induced Pluripotent Stem Cells (iPSCs) Derived 3D Human Lung Organoids from Different Ethnicities to Understand the SARS-CoV2 Severity/Infectivity Percentage. . 2021-02-00. Pubmed ID: 32500482; DOI: 10.1007/s12015-020-09989-2; PMC: PMC7272136 CSSi001-A 2021-02-00 2021-02-00 PubMed: 32500482 DOI: 10.1007/s12015-020-09989-2Associated cell lines:
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Dong Y, Long J, Luo X, Xie G, Xiao ZJ, Tong Y
Targeting of ΔNp63α by miR-522 promotes the migration of breast epithelial cells
Dong Y et al. Targeting of ΔNp63α by miR-522 promotes the migration of breast epithelial cells. . 2021-02-00. Pubmed ID: 33369228; DOI: 10.1002/2211-5463.13072; PMC: PMC7876488 WAe001-AWAe001-A-15 2021-02-00 2021-02-00 PubMed: 33369228 DOI: 10.1002/2211-5463.13072Associated cell lines:
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Hey CAB, Larsen LJ, Tümer Z, Brøndum-Nielsen K, Grønskov K, Hjortshøj TD, Møller LB
BBS Proteins Affect Ciliogenesis and Are Essential for Hedgehog Signaling, but Not for Formation of iPSC-Derived RPE-65 Expressing RPE-Like Cells
Hey CAB et al. BBS Proteins Affect Ciliogenesis and Are Essential for Hedgehog Signaling, but Not for Formation of iPSC-Derived RPE-65 Expressing RPE-Like Cells. . 2021-01-29. Pubmed ID: 33572860; DOI: 10.3390/ijms22031345; PMC: PMC7866284 KCi001-AKCi002-A 2021-01-29 2021-01-29 PubMed: 33572860 DOI: 10.3390/ijms22031345 -
Sorriento D, Iaccarino G
The Cardiovascular Phenotype in Fabry Disease: New Findings in the Research Field
Sorriento D et al. The Cardiovascular Phenotype in Fabry Disease: New Findings in the Research Field. . 2021-01-29. Pubmed ID: 33572752; DOI: 10.3390/ijms22031331; PMC: PMC7865937 INSAi002-A 2021-01-29 2021-01-29 PubMed: 33572752 DOI: 10.3390/ijms22031331Associated cell lines:
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Moya-Garzon MD, Gomez-Vidal JA, Alejo-Armijo A, Altarejos J, Rodriguez-Madoz JR, Fernandes MX, Salido E, Salido S, Diaz-Gavilan M
Small Molecule-Based Enzyme Inhibitors in the Treatment of Primary Hyperoxalurias
Moya-Garzon MD et al. Small Molecule-Based Enzyme Inhibitors in the Treatment of Primary Hyperoxalurias. . 2021-01-27. Pubmed ID: 33513899; DOI: 10.3390/jpm11020074; PMC: PMC7912158 CIMAi001-A 2021-01-27 2021-01-27 PubMed: 33513899 DOI: 10.3390/jpm11020074Associated cell lines:
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Böhnke J, Pinkert S, Schmidt M, Binder H, Bilz NC, Jung M, Reibetanz U, Beling A, Rujescu D, Claus C
Coxsackievirus B3 Infection of Human iPSC Lines and Derived Primary Germ-Layer Cells Regarding Receptor Expression
Böhnke J et al. Coxsackievirus B3 Infection of Human iPSC Lines and Derived Primary Germ-Layer Cells Regarding Receptor Expression. . 2021-01-27. Pubmed ID: 33513663; DOI: 10.3390/ijms22031220; PMC: PMC7865966 WISCi004-ATMOi001-A 2021-01-27 2021-01-27 PubMed: 33513663 DOI: 10.3390/ijms22031220Associated cell lines:
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Burkert K, Taheri H, Hamad S, Oliverio M, Peinkofer G, Kornfeld JW, Harnying W, Pfannkuche K, Hescheler J, Berkessel A, Šarić T
Salicylic diamines selectively eliminate residual undifferentiated cells from pluripotent stem cell-derived cardiomyocyte preparations
Burkert K et al. Salicylic diamines selectively eliminate residual undifferentiated cells from pluripotent stem cell-derived cardiomyocyte preparations. . 2021-01-27. Pubmed ID: 33504837; DOI: 10.1038/s41598-021-81351-z; PMC: PMC7841182 UKKi007-A 2021-01-27 2021-01-27 PubMed: 33504837 DOI: 10.1038/s41598-021-81351-zAssociated cell lines:
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Alonso-Barroso E, Pérez B, Desviat LR, Richard E
Cardiomyocytes Derived from Induced Pluripotent Stem Cells as a Disease Model for Propionic Acidemia
Alonso-Barroso E et al. Cardiomyocytes Derived from Induced Pluripotent Stem Cells as a Disease Model for Propionic Acidemia. . 2021-01-25. Pubmed ID: 33503868; DOI: 10.3390/ijms22031161; PMC: PMC7865492 UAMi001-A 2021-01-25 2021-01-25 PubMed: 33503868 DOI: 10.3390/ijms22031161Associated cell lines:
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Wu S.
Research progress in differentiation of male germ cells derived from induced pluripotent stem cells in vitro
Wu S.. Research progress in differentiation of male germ cells derived from induced pluripotent stem cells in vitro. . 2021-01-25. DOI: 10.3760/cma.j.cn101441-20200111-00021 HUSTi001-A 2021-01-25 2021-01-25 DOI: 10.3760/cma.j.cn101441-20200111-00021Associated cell lines:
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Ronchi C, Bernardi J, Mura M, Stefanello M, Badone B, Rocchetti M, Crotti L, Brink P, Schwartz PJ, Gnecchi M, Zaza A
NOS1AP polymorphisms reduce NOS1 activity and interact with prolonged repolarization in arrhythmogenesis
Ronchi C et al. NOS1AP polymorphisms reduce NOS1 activity and interact with prolonged repolarization in arrhythmogenesis. . 2021-01-21. Pubmed ID: 32061134; DOI: 10.1093/cvr/cvaa036; PMC: PMC7820868 PSMi007-A 2021-01-21 2021-01-21 PubMed: 32061134 DOI: 10.1093/cvr/cvaa036Associated cell lines:
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Elsayed AK, Younis I, Ali G, Hussain K, Abdelalim EM
Aberrant development of pancreatic beta cells derived from human iPSCs with FOXA2 deficiency
Elsayed AK et al. Aberrant development of pancreatic beta cells derived from human iPSCs with FOXA2 deficiency. . 2021-01-20. Pubmed ID: 33473118; DOI: 10.1038/s41419-021-03390-8; PMC: PMC7817686 QBRIi009-A 2021-01-20 2021-01-20 PubMed: 33473118 DOI: 10.1038/s41419-021-03390-8Associated cell lines:
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Kulikova O, Brodehl A, Kiseleva A, Myasnikov R, Meshkov A, Stanasiuk C, Gärtner A, Divashuk M, Sotnikova E, Koretskiy S, Kharlap M, Kozlova V, Mershina E, Pilus P, Sinitsyn V, Milting H, Boytsov S, Drapkina O
The Desmin (DES) Mutation p.A337P Is Associated with Left-Ventricular Non-Compaction Cardiomyopathy
Kulikova O et al. The Desmin (DES) Mutation p.A337P Is Associated with Left-Ventricular Non-Compaction Cardiomyopathy. . 2021-01-19. Pubmed ID: 33478057; DOI: 10.3390/genes12010121; PMC: PMC7835827 UKKi011-A 2021-01-19 2021-01-19 PubMed: 33478057 DOI: 10.3390/genes12010121Associated cell lines:
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Lau S, Gossen M, Lendlein A, Jung F
Venous and Arterial Endothelial Cells from Human Umbilical Cords: Potential Cell Sources for Cardiovascular Research
Lau S et al. Venous and Arterial Endothelial Cells from Human Umbilical Cords: Potential Cell Sources for Cardiovascular Research. . 2021-01-19. Pubmed ID: 33478148; DOI: 10.3390/ijms22020978; PMC: PMC7835953 IHSTMi001-A 2021-01-19 2021-01-19 PubMed: 33478148 DOI: 10.3390/ijms22020978Associated cell lines:
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García-López M, Arenas J, Gallardo ME
Hereditary Optic Neuropathies: Induced Pluripotent Stem Cell-Based 2D/3D Approaches
García-López M et al. Hereditary Optic Neuropathies: Induced Pluripotent Stem Cell-Based 2D/3D Approaches. . 2021-01-18. Pubmed ID: 33477675; DOI: 10.3390/genes12010112; PMC: PMC7831942 IISHDOi003-AFINCBi001-AIISHDOi006-A 2021-01-18 2021-01-18 PubMed: 33477675 DOI: 10.3390/genes12010112Associated cell lines:
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Yuan F, Xu Y, You K, Zhang J, Yang F, Li YX
Calcitriol alleviates ethanol-induced hepatotoxicity via AMPK/mTOR-mediated autophagy
Yuan F et al. Calcitriol alleviates ethanol-induced hepatotoxicity via AMPK/mTOR-mediated autophagy. . 2021-01-15. Pubmed ID: 33232716; DOI: 10.1016/j.abb.2020.108694 WAe001-AWAe001-A-12 2021-01-15 2021-01-15 PubMed: 33232716 DOI: 10.1016/j.abb.2020.108694Associated cell lines:
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Crawford LB, Hancock MH, Struthers HM, Streblow DN, Yurochko AD, Caposio P, Goodrum FD, Nelson JA
CD34(+) Hematopoietic Progenitor Cell Subsets Exhibit Differential Ability To Maintain Human Cytomegalovirus Latency and Persistence
Crawford LB et al. CD34(+) Hematopoietic Progenitor Cell Subsets Exhibit Differential Ability To Maintain Human Cytomegalovirus Latency and Persistence. . 2021-01-13. Pubmed ID: 33177198; DOI: 10.1128/jvi.02105-20; PMC: PMC7925096 WAe001-AWAe009-A 2021-01-13 2021-01-13 PubMed: 33177198 DOI: 10.1128/jvi.02105-20 -
Nilsson F, Storm P, Sozzi E, Hidalgo Gil D, Birtele M, Sharma Y, Parmar M, Fiorenzano A
Single-Cell Profiling of Coding and Noncoding Genes in Human Dopamine Neuron Differentiation
Nilsson F et al. Single-Cell Profiling of Coding and Noncoding Genes in Human Dopamine Neuron Differentiation. . 2021-01-12. Pubmed ID: 33445654; DOI: 10.3390/cells10010137; PMC: PMC7827700 RCe021-A 2021-01-12 2021-01-12 PubMed: 33445654 DOI: 10.3390/cells10010137Associated cell lines:
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Völkner C, Liedtke M, Hermann A, Frech MJ
Pluripotent Stem Cells for Disease Modeling and Drug Discovery in Niemann-Pick Type C1
Völkner C et al. Pluripotent Stem Cells for Disease Modeling and Drug Discovery in Niemann-Pick Type C1. . 2021-01-12. Pubmed ID: 33445799; DOI: 10.3390/ijms22020710; PMC: PMC7828283 AKOSi001-ATRNDi001-DAKOSi004-AAKOSi005-AAKOSi006-AAKOSi007-A 2021-01-12 2021-01-12 PubMed: 33445799 DOI: 10.3390/ijms22020710Associated cell lines:
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Arber C, Lovejoy C, Harris L, Willumsen N, Alatza A, Casey JM, Lines G, Kerins C, Mueller AK, Zetterberg H, Hardy J, Ryan NS, Fox NC, Lashley T, Wray S
Familial Alzheimer's Disease Mutations in PSEN1 Lead to Premature Human Stem Cell Neurogenesis
Arber C et al. Familial Alzheimer's Disease Mutations in PSEN1 Lead to Premature Human Stem Cell Neurogenesis. . 2021-01-12. Pubmed ID: 33440141; DOI: 10.1016/j.celrep.2020.108615; PMC: PMC7809623 RBi001-A 2021-01-12 2021-01-12 PubMed: 33440141 DOI: 10.1016/j.celrep.2020.108615Associated cell lines:
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Li B, Ye F, Chen L, Yang X, Zhang J, Luo Y, Xu J, Luo Y, Wang S
Generation of two induced pluripotent stem cell lines SPPHi001-A and SPPHi002-A from a Huntington's disease family of Southwestern China
Li B et al. Generation of two induced pluripotent stem cell lines SPPHi001-A and SPPHi002-A from a Huntington's disease family of Southwestern China. . 2021-01-04. Pubmed ID: 33429129; DOI: 10.1016/j.scr.2020.102149 SPPHIi001-ASPPHIi002-A 2021-01-04 2021-01-04 PubMed: 33429129 DOI: 10.1016/j.scr.2020.102149Associated cell lines:
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Peron C, Mauceri R, Iannielli A, Cavaliere A, Legati A, Rizzo A, Sciacca FL, Broccoli V, Tiranti V
Generation of two human iPSC lines, FINCBi002-A and FINCBi003-A, carrying heteroplasmic macrodeletion of mitochondrial DNA causing Pearson's syndrome
Peron C et al. Generation of two human iPSC lines, FINCBi002-A and FINCBi003-A, carrying heteroplasmic macrodeletion of mitochondrial DNA causing Pearson's syndrome. . 2021-01-04. Pubmed ID: 33434818; DOI: 10.1016/j.scr.2020.102151 FINCBi002-AFINCBi003-A 2021-01-04 2021-01-04 PubMed: 33434818 DOI: 10.1016/j.scr.2020.102151Associated cell lines:
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Reinert LS, Rashidi AS, Tran DN, Katzilieris-Petras G, Hvidt AK, Gohr M, Fruhwürth S, Bodda C, Thomsen MK, Vendelbo MH, Khan AR, Hansen B, Bergström P, Agholme L, Mogensen TH, Christensen MH, Nyengaard JR, Sen GC, Zetterberg H, Verjans GM, Paludan SR
Brain immune cells undergo cGAS/STING-dependent apoptosis during herpes simplex virus type 1 infection to limit type I IFN production
Reinert LS et al. Brain immune cells undergo cGAS/STING-dependent apoptosis during herpes simplex virus type 1 infection to limit type I IFN production. . 2021-01-04. Pubmed ID: 32990676; DOI: 10.1172/jci136824; PMC: PMC7773356 WTSIi015-A 2021-01-04 2021-01-04 PubMed: 32990676 DOI: 10.1172/jci136824Associated cell lines:
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Hang C, Song Y, Wu F, Dong T, Jiang M, Saleem A, Zhang S, Chang Y, Lu W, Cui M
Generation of a homozygous COX6A2 knockout human embryonic stem cell line (WAe009-A-47) via an epiCRISPR/Cas9 system
Hang C et al. Generation of a homozygous COX6A2 knockout human embryonic stem cell line (WAe009-A-47) via an epiCRISPR/Cas9 system. . 2021-01-04. Pubmed ID: 33418201; DOI: 10.1016/j.scr.2020.102152 WAe009-AWAe009-A-47 2021-01-04 2021-01-04 PubMed: 33418201 DOI: 10.1016/j.scr.2020.102152Associated cell lines:
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Fiorenzano A, Birtele M, Wahlestedt J, Parmar M.
Evaluation of TH-Cre knock-in cell lines for detection and specific targeting of stem cell-derived dopaminergic neurons
Fiorenzano A et al. Evaluation of TH-Cre knock-in cell lines for detection and specific targeting of stem cell-derived dopaminergic neurons. . 2021-01-01. RCe021-A 2021-01-01 2021-01-01Associated cell lines:
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Subash SK, Kumar PG
Spermatogonial stem cells: A story of self-renewal and differentiation
Subash SK et al. Spermatogonial stem cells: A story of self-renewal and differentiation. . 2021-01-01. Pubmed ID: 33049667; DOI: 10.2741/4891 MUSIi006-A 2021-01-01 2021-01-01 PubMed: 33049667 DOI: 10.2741/4891Associated cell lines:
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Goldeman C, Andersen M, Al-Robai A, Buchholtz T, Svane N, Ozgür B, Holst B, Shusta E, Hall VJ, Saaby L, Hyttel P, Brodin B
Human induced pluripotent stem cells (BIONi010-C) generate tight cell monolayers with blood-brain barrier traits and functional expression of large neutral amino acid transporter 1 (SLC7A5)
Goldeman C et al. Human induced pluripotent stem cells (BIONi010-C) generate tight cell monolayers with blood-brain barrier traits and functional expression of large neutral amino acid transporter 1 (SLC7A5). . 2021-01-01. Pubmed ID: 33011235; DOI: 10.1016/j.ejps.2020.105577 BIONi010-C 2021-01-01 2021-01-01 PubMed: 33011235 DOI: 10.1016/j.ejps.2020.105577Associated cell lines:
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Zhu L.
Advances in the Application of High-throughput Screening Techniques Based on Cell Models in Drug Development
Zhu L.. Advances in the Application of High-throughput Screening Techniques Based on Cell Models in Drug Development. . 2021-01-01. DOI: 10.13748/j.cnki.issn1007-7693.2021.23.023 WMUi001-A 2021-01-01 2021-01-01 DOI: 10.13748/j.cnki.issn1007-7693.2021.23.023Associated cell lines:
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Fiorenzano A, Birtele M, Wahlestedt JN, Parmar M
Evaluation of TH-Cre knock-in cell lines for detection and specific targeting of stem cell-derived dopaminergic neurons
Fiorenzano A et al. Evaluation of TH-Cre knock-in cell lines for detection and specific targeting of stem cell-derived dopaminergic neurons. . 2021-01-00. Pubmed ID: 33532642; DOI: 10.1016/j.heliyon.2021.e06006; PMC: PMC7821040 RCe021-A 2021-01-00 2021-01-00 PubMed: 33532642 DOI: 10.1016/j.heliyon.2021.e06006Associated cell lines:
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Zhang X, Ding J, Xia S
A preliminary study of MMP-9 and sCD40L in patients with coronary slow flow
Zhang X et al. A preliminary study of MMP-9 and sCD40L in patients with coronary slow flow. . 2021-01-00. Pubmed ID: 33545794; DOI: 10.21037/apm-20-2271 SYSUi002-A 2021-01-00 2021-01-00 PubMed: 33545794 DOI: 10.21037/apm-20-2271Associated cell lines:
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Iismaa SE, Hesselson S, McGrath-Cadell L, Muller DW, Fatkin D, Giannoulatou E, Kovacic J, Graham RM
Spontaneous Coronary Artery Dissection and Fibromuscular Dysplasia: Vasculopathies With a Predilection for Women
Iismaa SE et al. Spontaneous Coronary Artery Dissection and Fibromuscular Dysplasia: Vasculopathies With a Predilection for Women. . 2021-01-00. Pubmed ID: 32713767; DOI: 10.1016/j.hlc.2020.05.110; PMC: PMC7710561 VCCRIi001-A 2021-01-00 2021-01-00 PubMed: 32713767 DOI: 10.1016/j.hlc.2020.05.110Associated cell lines:
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Li T, Jin W, He Y, Zhou Z
Generation of PRMT6 homozygous knockout human embryonic stem cell lines
Li T et al. Generation of PRMT6 homozygous knockout human embryonic stem cell lines. . 2020-12-28. Pubmed ID: 33383404; DOI: 10.1016/j.scr.2020.102136 HKUe001-AHKUe001-A-1 2020-12-28 2020-12-28 PubMed: 33383404 DOI: 10.1016/j.scr.2020.102136Associated cell lines:
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Alowaysi M, Astro V, Fiacco E, Alzahrani F, Alkuraya FS, Adamo A
Generation of iPSC lines (KAUSTi011-A, KAUSTi011-B) from a Saudi patient with epileptic encephalopathy carrying homozygous mutation in the GLP1R gene
Alowaysi M et al. Generation of iPSC lines (KAUSTi011-A, KAUSTi011-B) from a Saudi patient with epileptic encephalopathy carrying homozygous mutation in the GLP1R gene. . 2020-12-28. Pubmed ID: 33421754; DOI: 10.1016/j.scr.2020.102148 KAUSTi003-AKAUSTi004-AKAUSTi004-BKAUSTi005-AKAUSTi005-BKAUSTi005-CKAUSTi011-AKAUSTi011-B 2020-12-28 2020-12-28 PubMed: 33421754 DOI: 10.1016/j.scr.2020.102148Associated cell lines:
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Wang B, Liu C, Zhang H, Gai Z, Liu Y
An induced pluripotent stem cell line (SDQLCHi033-A) derived from a patient with maple syrup urine disease type Ib carrying a homozygous mutation in BCKDHB gene
Wang B et al. An induced pluripotent stem cell line (SDQLCHi033-A) derived from a patient with maple syrup urine disease type Ib carrying a homozygous mutation in BCKDHB gene. . 2020-12-28. Pubmed ID: 33388706; DOI: 10.1016/j.scr.2020.102146 SDQLCHi033-A 2020-12-28 2020-12-28 PubMed: 33388706 DOI: 10.1016/j.scr.2020.102146Associated cell lines:
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Wang M, Ruan Y, Tian X, Liu Y, Liu M, Fu W, Du W, Zhao J, Hu L, Li X, Zhao X, Dong J
Generation of a hiPSC line ZZUNEUi012-A from a healthy female individual
Wang M et al. Generation of a hiPSC line ZZUNEUi012-A from a healthy female individual. . 2020-12-26. Pubmed ID: 33418203; DOI: 10.1016/j.scr.2020.102143 ZZUNEUi007-AZZUNEUi012-A 2020-12-26 2020-12-26 PubMed: 33418203 DOI: 10.1016/j.scr.2020.102143Associated cell lines:
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Wang L, Li X, Fu W, Zhang S, Du W, Zhao J, Liu M, Wang M, Liu Y, Hu L, Ding Z, Li L, Zhao X, Dong J
Generation of an IPSC line from a patient with hypertrophic cardiomyopathy carrying a mutation in MYH6 gene
Wang L et al. Generation of an IPSC line from a patient with hypertrophic cardiomyopathy carrying a mutation in MYH6 gene. . 2020-12-24. Pubmed ID: 33385793; DOI: 10.1016/j.scr.2020.102138 ZZUNEUi013-A 2020-12-24 2020-12-24 PubMed: 33385793 DOI: 10.1016/j.scr.2020.102138Associated cell lines:
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Quan Y, Zhang T, Zhang H, Yang J, Jin P, Ma J, Fan Y, Fan J, Fan X, Gong Y, Li M, Wang Y
Generation of a human embryonic stem cell (WAe001-A-47) with hVGLL4 doxycyclin-inducible expression by the PiggyBac transposon system
Quan Y et al. Generation of a human embryonic stem cell (WAe001-A-47) with hVGLL4 doxycyclin-inducible expression by the PiggyBac transposon system. . 2020-12-24. Pubmed ID: 33385792; DOI: 10.1016/j.scr.2020.102142 WAe001-AWMUi001-AWAe001-A-47 2020-12-24 2020-12-24 PubMed: 33385792 DOI: 10.1016/j.scr.2020.102142Associated cell lines:
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Fu W, Wang M, Liu Y, Liu M, Wang L, Hu L, Zhao X, Ding Z, Li X, Dong J
Induced pluripotent stem cell line (ZZUNEUi011-A) derived from peripheral blood mononuclear cells (PBMCs) of a healthy 27-year-old female individual
Fu W et al. Induced pluripotent stem cell line (ZZUNEUi011-A) derived from peripheral blood mononuclear cells (PBMCs) of a healthy 27-year-old female individual. . 2020-12-24. Pubmed ID: 33383407; DOI: 10.1016/j.scr.2020.102139 ZZUNEUi011-A 2020-12-24 2020-12-24 PubMed: 33383407 DOI: 10.1016/j.scr.2020.102139Associated cell lines:
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Medina DX, Boehringer A, Dominick M, Lorenzini I, Saez-Atienzar S, Pioro EP, Sattler R, Traynor B, Bowser R
Generation of two induced pluripotent stem cell (iPSC) lines from an ALS patient with simultaneous mutations in KIF5A and MATR3 genes
Medina DX et al. Generation of two induced pluripotent stem cell (iPSC) lines from an ALS patient with simultaneous mutations in KIF5A and MATR3 genes. . 2020-12-24. Pubmed ID: 33388707; DOI: 10.1016/j.scr.2020.102141; PMC: PMC8222416 BNIi001-ABNIi001-B 2020-12-24 2020-12-24 PubMed: 33388707 DOI: 10.1016/j.scr.2020.102141 -
Reé D, Borsy A, Fóthi Á, Orbán TI, Várady G, Erdei Z, Sarkadi B, Réthelyi J, Varga N, Apáti Á
Establishing a human embryonic stem cell clone with a heterozygous mutation in the DGCR8 gene
Reé D et al. Establishing a human embryonic stem cell clone with a heterozygous mutation in the DGCR8 gene. . 2020-12-22. Pubmed ID: 33360445; DOI: 10.1016/j.scr.2020.102134 HVRDe009-AHVRDe009-A-1 2020-12-22 2020-12-22 PubMed: 33360445 DOI: 10.1016/j.scr.2020.102134Associated cell lines:
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van IJzendoorn DGP, Salvatori DCF, Cao X, van den Hil F, Briaire-de Bruijn IH, de Jong D, Mei H, Mummery CL, Szuhai K, Bovée JVMG, Orlova VV
Vascular Tumor Recapitulated in Endothelial Cells from hiPSCs Engineered to Express the SERPINE1-FOSB Translocation
van IJzendoorn DGP et al. Vascular Tumor Recapitulated in Endothelial Cells from hiPSCs Engineered to Express the SERPINE1-FOSB Translocation. . 2020-12-22. Pubmed ID: 33377124; DOI: 10.1016/j.xcrm.2020.100153; PMC: PMC7762773 LUMCi001-A 2020-12-22 2020-12-22 PubMed: 33377124 DOI: 10.1016/j.xcrm.2020.100153Associated cell lines:
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Merkert S, Jaboreck MC, Engels L, Malik MNH, Göhring G, Pessler F, Martin U, Olmer R
Generation of two human ISG15 knockout iPSC clones using CRISPR/Cas9 editing
Merkert S et al. Generation of two human ISG15 knockout iPSC clones using CRISPR/Cas9 editing. . 2020-12-22. Pubmed ID: 33383405; DOI: 10.1016/j.scr.2020.102135 MHHi001-A-3MHHi001-A-4 2020-12-22 2020-12-22 PubMed: 33383405 DOI: 10.1016/j.scr.2020.102135Associated cell lines:
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Cheng YS, Yang S, Hong J, Li R, Beers J, Zou J, Huang W, Zheng W
Modeling CNS Involvement in Pompe Disease Using Neural Stem Cells Generated from Patient-Derived Induced Pluripotent Stem Cells
Cheng YS et al. Modeling CNS Involvement in Pompe Disease Using Neural Stem Cells Generated from Patient-Derived Induced Pluripotent Stem Cells. . 2020-12-22. Pubmed ID: 33375166; DOI: 10.3390/cells10010008; PMC: PMC7822217 TRNDi007-BTRNDi028-A 2020-12-22 2020-12-22 PubMed: 33375166 DOI: 10.3390/cells10010008Associated cell lines:
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Gurevich I, Burton SA, Munn C, Ohshima M, Goedland ME, Czysz K, Rajesh D
iPSC-derived hepatocytes generated from NASH donors provide a valuable platform for disease modeling and drug discovery
Gurevich I et al. iPSC-derived hepatocytes generated from NASH donors provide a valuable platform for disease modeling and drug discovery. . 2020-12-16. Pubmed ID: 33268331; DOI: 10.1242/bio.055087; PMC: PMC7758638 CDIi001-ACIRMi06T-ACIRMi07H-ACIRMi07J-ACIRMi07L-ACIRMi11H-ACIRMi11L-ACIRMi11M-A 2020-12-16 2020-12-16 PubMed: 33268331 DOI: 10.1242/bio.055087Associated cell lines:
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Hao E, Zhang G, Mu L, Ma N, Wang T
Establishment of a human MYH6 compound heterozygous knockout hESC line to model cardiomyopathy and congenital heart defects by CRISPR/Cas9 system
Hao E et al. Establishment of a human MYH6 compound heterozygous knockout hESC line to model cardiomyopathy and congenital heart defects by CRISPR/Cas9 system. . 2020-12-16. Pubmed ID: 33360099; DOI: 10.1016/j.scr.2020.102128 WAe009-AWAe009-A-46 2020-12-16 2020-12-16 PubMed: 33360099 DOI: 10.1016/j.scr.2020.102128Associated cell lines:
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Zaw K, Wong EYM, Zhang X, Zhang D, Chen SC, Thompson JA, Lamey T, McLaren T, De Roach JN, Wilton SD, Fletcher S, Mitrpant C, Atlas MD, Chen FK, McLenachan S
Generation of three induced pluripotent stem cell lines from a patient with Usher syndrome caused by biallelic c.949C > A and c.1256G > T mutations in the USH2A gene
Zaw K et al. Generation of three induced pluripotent stem cell lines from a patient with Usher syndrome caused by biallelic c.949C > A and c.1256G > T mutations in the USH2A gene. . 2020-12-16. Pubmed ID: 33360097; DOI: 10.1016/j.scr.2020.102129 LEIi014-ALEIi014-BLEIi014-C 2020-12-16 2020-12-16 PubMed: 33360097 DOI: 10.1016/j.scr.2020.102129 -
Siehler J, Blöchinger AK, Akgün M, Wang X, Shahryari A, Geerlof A, Lickert H, Burtscher I
Generation of a heterozygous C-peptide-mCherry reporter human iPSC line (HMGUi001-A-8)
Siehler J et al. Generation of a heterozygous C-peptide-mCherry reporter human iPSC line (HMGUi001-A-8). . 2020-12-16. Pubmed ID: 33373890; DOI: 10.1016/j.scr.2020.102126 HMGUi001-AHMGUi001-A-8 2020-12-16 2020-12-16 PubMed: 33373890 DOI: 10.1016/j.scr.2020.102126Associated cell lines:
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Völkner C, Liedtke M, Petters J, Lukas J, Murua Escobar H, Knuebel G, Bullerdiek J, Holzmann C, Hermann A, Frech MJ, US Food and Drug Administration Interviewees, Robyn Bent R, Bocell F, Garrard L, Johnson LL, Knoble N, Reasner D, Tarver M, Weinfurt K, Mullin T
Generation of an iPSC line (AKOSi004-A) from fibroblasts of a female adult NPC1 patient, carrying the compound heterozygous mutation p.Val1023Serfs*15/p.Gly992Arg and of an iPSC line (AKOSi005-A) from a female adult control individual
Völkner C et al. Generation of an iPSC line (AKOSi004-A) from fibroblasts of a female adult NPC1 patient, carrying the compound heterozygous mutation p.Val1023Serfs*15/p.Gly992Arg and of an iPSC line (AKOSi005-A) from a female adult control individual. . 2020-12-15. Pubmed ID: 33360098; DOI: 10.1016/j.scr.2020.102127 AKOSi004-AAKOSi005-A 2020-12-15 2020-12-15 PubMed: 33360098 DOI: 10.1016/j.scr.2020.102127Associated cell lines:
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Page A, Fusil F, Cosset FL
Toward Tightly Tuned Gene Expression Following Lentiviral Vector Transduction
Page A et al. Toward Tightly Tuned Gene Expression Following Lentiviral Vector Transduction. . 2020-12-11. Pubmed ID: 33322556; DOI: 10.3390/v12121427; PMC: PMC7764518 NERCe003-ANERCe003-A-1 2020-12-11 2020-12-11 PubMed: 33322556 DOI: 10.3390/v12121427Associated cell lines:
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Gao X, Liao X, Zhang J, Lin J, Tan M
Derivation of an induced pluripotent stem cell line (GWCMCi001-A) from PBMCs of a four-year-old male patient with Immunoglobulin A nephropathy
Gao X et al. Derivation of an induced pluripotent stem cell line (GWCMCi001-A) from PBMCs of a four-year-old male patient with Immunoglobulin A nephropathy. . 2020-12-10. Pubmed ID: 33359895; DOI: 10.1016/j.scr.2020.102123 GWCMCi001-A 2020-12-10 2020-12-10 PubMed: 33359895 DOI: 10.1016/j.scr.2020.102123Associated cell lines:
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Kung LHW, Sampurno L, Little CB, Lamandé SR, Bateman JF
Generation of a miR-26b stem-loop knockout human iPSC line, MCRIi019-A-1, using CRISPR/Cas9 editing
Kung LHW et al. Generation of a miR-26b stem-loop knockout human iPSC line, MCRIi019-A-1, using CRISPR/Cas9 editing. . 2020-12-10. Pubmed ID: 33316599; DOI: 10.1016/j.scr.2020.102118 MCRIi019-AMCRIi019-A-1MCRIi019-A-2 2020-12-10 2020-12-10 PubMed: 33316599 DOI: 10.1016/j.scr.2020.102118Associated cell lines:
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Fiacco E, Alowaysi M, Astro V, Adamo A
Generation of an iPSC cohort of isogenic iPSC lines (46-XY and 47-XXY) from a non-mosaic Klinefelter Syndrome patient (47-XXY) (KAUSTi008-A, KAUSTi008-B, KAUSTi008-C, KAUSTi008-D, KAUSTi008-E, KAUSTi008-F, KAUSTi008-G)
Fiacco E et al. Generation of an iPSC cohort of isogenic iPSC lines (46-XY and 47-XXY) from a non-mosaic Klinefelter Syndrome patient (47-XXY) (KAUSTi008-A, KAUSTi008-B, KAUSTi008-C, KAUSTi008-D, KAUSTi008-E, KAUSTi008-F, KAUSTi008-G). . 2020-12-10. Pubmed ID: 33333453; DOI: 10.1016/j.scr.2020.102119 KAUSTi003-AKAUSTi004-AKAUSTi004-BKAUSTi005-AKAUSTi005-BKAUSTi005-CKAUSTi006-AKAUSTi006-BKAUSTi008-AKAUSTi008-BKAUSTi008-CKAUSTi008-DKAUSTi008-EKAUSTi008-FKAUSTi008-GKAUSTi008-F-1KAUSTi008-F-2 2020-12-10 2020-12-10 PubMed: 33333453 DOI: 10.1016/j.scr.2020.102119 -
Thakur P, Bhargava N, Jaitly S, Gupta P, Kumar Bhattacharya S, Padma G, Kondaveeti S, Jain S, Ramalingam S
Establishment and characterization of induced pluripotent stem cell line (IGIBi002-A) from a β-thalassemia patient with IVS1-5 mutation by non-integrating reprogramming approach
Thakur P et al. Establishment and characterization of induced pluripotent stem cell line (IGIBi002-A) from a β-thalassemia patient with IVS1-5 mutation by non-integrating reprogramming approach. . 2020-12-10. Pubmed ID: 33338925; DOI: 10.1016/j.scr.2020.102124 IGIBi001-AIGIBi002-A 2020-12-10 2020-12-10 PubMed: 33338925 DOI: 10.1016/j.scr.2020.102124Associated cell lines:
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Zhou M, Wei R, Jiang Y, Fu J, Liu Y, Yang B, Yu B, Lin Y, Ran X, Lai WH, Chu M, Hu Y, Yang J, Tse HF
Generation of a human iPSC line GIBHi002-A-2 with a dual-reporter for NKX2-5 using TALENs
Zhou M et al. Generation of a human iPSC line GIBHi002-A-2 with a dual-reporter for NKX2-5 using TALENs. . 2020-12-10. Pubmed ID: 33352530; DOI: 10.1016/j.scr.2020.102120 GIBHi002-AGIBHi002-A-2 2020-12-10 2020-12-10 PubMed: 33352530 DOI: 10.1016/j.scr.2020.102120Associated cell lines:
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Zhang T, Huang W, Xue X
Generation of a FOXH1 homozygous knockout human embryonic stem cell line by CRISPR/Cas9 system
Zhang T et al. Generation of a FOXH1 homozygous knockout human embryonic stem cell line by CRISPR/Cas9 system. . 2020-12-10. Pubmed ID: 33348200; DOI: 10.1016/j.scr.2020.102121 WAe009-AWAe009-A-42 2020-12-10 2020-12-10 PubMed: 33348200 DOI: 10.1016/j.scr.2020.102121Associated cell lines:
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Kashevarova AA, Nikitina TV, Mikhailik LI, Belyaeva EO, Vasilyev SA, Lopatkina ME, Fedotov DA, Fonova EA, Zarubin AA, Sivtsev AA, Skryabin NA, Nazarenko LP, Lebedev IN
46,XY,r(8)/45,XY,-8 Mosaicism as a Possible Mechanism of the Imprinted Birk-Barel Syndrome: A Case Study
Kashevarova AA et al. 46,XY,r(8)/45,XY,-8 Mosaicism as a Possible Mechanism of the Imprinted Birk-Barel Syndrome: A Case Study. . 2020-12-09. Pubmed ID: 33316910; DOI: 10.3390/genes11121473; PMC: PMC7763634 ICGi025-A 2020-12-09 2020-12-09 PubMed: 33316910 DOI: 10.3390/genes11121473Associated cell lines:
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Vasylovska S, Schuster J, Brboric A, Carlsson PO, Dahl N, Lau J
Generation of human induced pluripotent stem cell (iPSC) lines (UUMCBi001-A, UUMCBi002-A) from two healthy donors
Vasylovska S et al. Generation of human induced pluripotent stem cell (iPSC) lines (UUMCBi001-A, UUMCBi002-A) from two healthy donors. . 2020-12-09. Pubmed ID: 33340796; DOI: 10.1016/j.scr.2020.102114 UUMCBi001-AUUMCBi002-A 2020-12-09 2020-12-09 PubMed: 33340796 DOI: 10.1016/j.scr.2020.102114Associated cell lines:
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Leavens KF, Liao CM, Gagne AL, Kishore S, Cardenas-Diaz FL, French DL, Gadue P
Generation of a double insulin and somatostatin reporter line, SCSe001-A-3, for the advancement of stem cell-derived pancreatic islets
Leavens KF et al. Generation of a double insulin and somatostatin reporter line, SCSe001-A-3, for the advancement of stem cell-derived pancreatic islets. . 2020-12-08. Pubmed ID: 33316598; DOI: 10.1016/j.scr.2020.102112; PMC: PMC8546798 SCSe001-ACHOPi002-ACHOPi003-ASCSe001-A-3 2020-12-08 2020-12-08 PubMed: 33316598 DOI: 10.1016/j.scr.2020.102112Associated cell lines:
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Cui Y, Wang J, Zhang G, Luan J, Han J
Generation of an induced pluripotent stem cell line SMBCi010-A from a male with Multiple Osteochondroma carrying a EXT1 mutation
Cui Y et al. Generation of an induced pluripotent stem cell line SMBCi010-A from a male with Multiple Osteochondroma carrying a EXT1 mutation. . 2020-12-07. Pubmed ID: 33360848; DOI: 10.1016/j.scr.2020.102111 SMBCi010-A 2020-12-07 2020-12-07 PubMed: 33360848 DOI: 10.1016/j.scr.2020.102111Associated cell lines:
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Lito S, Sidibe A, Ilmjarv S, Burda P, Baumgartner M, Wehrle-Haller B, Krause KH, Marteyn A
Induced Pluripotent Stem Cells to Understand Mucopolysaccharidosis. I: Demonstration of a Migration Defect in Neural Precursors
Lito S et al. Induced Pluripotent Stem Cells to Understand Mucopolysaccharidosis. I: Demonstration of a Migration Defect in Neural Precursors. . 2020-12-03. Pubmed ID: 33287330; DOI: 10.3390/cells9122593; PMC: PMC7761689 UNIGEi001-A 2020-12-03 2020-12-03 PubMed: 33287330 DOI: 10.3390/cells9122593Associated cell lines:
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Sheeler C, Rosa JG, Ferro A, McAdams B, Borgenheimer E, Cvetanovic M
Glia in Neurodegeneration: The Housekeeper, the Defender and the Perpetrator
Sheeler C et al. Glia in Neurodegeneration: The Housekeeper, the Defender and the Perpetrator. . 2020-12-02. Pubmed ID: 33276471; DOI: 10.3390/ijms21239188; PMC: PMC7730416 MUSIi007-A 2020-12-02 2020-12-02 PubMed: 33276471 DOI: 10.3390/ijms21239188Associated cell lines:
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Barnabei L, Castela M, Banal C, Lefort N, Rieux-Laucat F
Generation of an iPSC line (IMAGINi011-A) from a patient carrying a STING mutation
Barnabei L et al. Generation of an iPSC line (IMAGINi011-A) from a patient carrying a STING mutation. . 2020-12-02. Pubmed ID: 33340797; DOI: 10.1016/j.scr.2020.102107 IMAGINi011-A 2020-12-02 2020-12-02 PubMed: 33340797 DOI: 10.1016/j.scr.2020.102107Associated cell lines:
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Garcia-Diaz A, Efe G, Kabra K, Patel A, Lowry ER, Shneider NA, Corneo B, Wichterle H
Standardized Reporter Systems for Purification and Imaging of Human Pluripotent Stem Cell-derived Motor Neurons and Other Cholinergic Cells
Garcia-Diaz A et al. Standardized Reporter Systems for Purification and Imaging of Human Pluripotent Stem Cell-derived Motor Neurons and Other Cholinergic Cells. . 2020-12-01. Pubmed ID: 32615233; DOI: 10.1016/j.neuroscience.2020.06.028; PMC: PMC7688562 CRMi003-ACUIMCi002-A 2020-12-01 2020-12-01 PubMed: 32615233 DOI: 10.1016/j.neuroscience.2020.06.028Associated cell lines:
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Bugallo-Casal Ana, Pérez-Mato María, Campos Francisco
Present and future of adult stem cells and induced pluripotent stem cells therapy for ischemic stroke
Bugallo-Casal Ana et al. Present and future of adult stem cells and induced pluripotent stem cells therapy for ischemic stroke. . 2021-00-00. DOI: 10.1016/b978-0-12-822229-4.00014-0 IDISi001-A 2021-00-00 2021-00-00 DOI: 10.1016/b978-0-12-822229-4.00014-0Associated cell lines:
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Waite AJ, Millar D, Clarke A
The generation of an induced pluripotent stem cell line (DCGi001-A) from an individual with FOXG1 syndrome carrying the c.460dupG (p.Glu154fs) variation in the FOXG1 gene
Waite AJ et al. The generation of an induced pluripotent stem cell line (DCGi001-A) from an individual with FOXG1 syndrome carrying the c.460dupG (p.Glu154fs) variation in the FOXG1 gene. . 2020-12-00. Pubmed ID: 33096386; DOI: 10.1016/j.scr.2020.102018 DCGi001-A 2020-12-00 2020-12-00 PubMed: 33096386 DOI: 10.1016/j.scr.2020.102018Associated cell lines:
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Satoh T, Toledo MAS, Boehnke J, Olschok K, Flosdorf N, Götz K, Küstermann C, Sontag S, Seré K, Koschmieder S, Brümmendorf TH, Chatain N, Tagawa YI, Zenke M
Human DC3 Antigen Presenting Dendritic Cells From Induced Pluripotent Stem Cells
Satoh T et al. Human DC3 Antigen Presenting Dendritic Cells From Induced Pluripotent Stem Cells. . 2021-00-00. Pubmed ID: 34368123; DOI: 10.3389/fcell.2021.667304; PMC: PMC8339905 UKAi002-AUKAi002-BUKAi003-A 2021-00-00 2021-00-00 PubMed: 34368123 DOI: 10.3389/fcell.2021.667304 -
Nguyen D, Bharat V, Conradson DM, Nandakishore P, Wang X
Miro1 Impairment in a Parkinson's At-Risk Cohort
Nguyen D et al. Miro1 Impairment in a Parkinson's At-Risk Cohort. . 2021-00-00. Pubmed ID: 34434090; DOI: 10.3389/fnmol.2021.734273; PMC: PMC8381147 CDIi016-ACDIi019-ACDIi020-ACDIi022-ACDIi024-ACDIi025-ACDIi026-ACDIi030-ACDIi032-ACDIi034-ACDIi035-ACDIi036-ACDIi037-ACDIi038-ACDIi039-ACDIi041-ACDIi042-ACDIi043-ACDIi045-ACDIi048-ACDIi051-ACDIi054-ACDIi058-ACDIi059-ACDIi060-ACDIi061-ACDIi062-ACDIi070-ACDIi073-ACDIi074-ACDIi075-ACDIi076-ACDIi080-ACDIi081-ACDIi083-ACDIi084-ACDIi086-ACDIi091-ACDIi092-ACDIi094-ACDIi095-ACDIi096-ACDIi098-ACDIi099-ACDIi100-ACDIi101-ACDIi102-ACDIi103-ACDIi104-ACDIi105-A 2021-00-00 2021-00-00 PubMed: 34434090 DOI: 10.3389/fnmol.2021.734273 -
Ebner-Peking P, Krisch L, Wolf M, Hochmann S, Hoog A, Vári B, Muigg K, Poupardin R, Scharler C, Schmidhuber S, Russe E, Stachelscheid H, Schneeberger A, Schallmoser K, Strunk D
Self-assembly of differentiated progenitor cells facilitates spheroid human skin organoid formation and planar skin regeneration
Ebner-Peking P et al. Self-assembly of differentiated progenitor cells facilitates spheroid human skin organoid formation and planar skin regeneration. . 2021-00-00. Pubmed ID: 34373751; DOI: 10.7150/thno.59661; PMC: PMC8344006 BIHi001-A 2021-00-00 2021-00-00 PubMed: 34373751 DOI: 10.7150/thno.59661Associated cell lines:
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Ferguson Daniel C.J., MacInnes Katherine A., Daniels Deborah E., Frayne Jan
iPSC-derived erythroid cells
Ferguson Daniel C.J. et al. iPSC-derived erythroid cells. . 2021-00-00. DOI: 10.1016/b978-0-12-822230-0.00006-5 MUi009-A 2021-00-00 2021-00-00 DOI: 10.1016/b978-0-12-822230-0.00006-5Associated cell lines:
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Gautam S, Biswas S, Singh B, Guo Y, Deng P, Deng W
Urine Cells-derived iPSCs: An Upcoming Frontier in Regenerative Medicine
Gautam S et al. Urine Cells-derived iPSCs: An Upcoming Frontier in Regenerative Medicine. . 2021-00-00. Pubmed ID: 34165400; DOI: 10.2174/0929867328666210623142150 MUSIi005-ACSUASOi001-A 2021-00-00 2021-00-00 PubMed: 34165400 DOI: 10.2174/0929867328666210623142150Associated cell lines:
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Schäfer-Korting M, Zoschke C
How Qualification of 3D Disease Models Cuts the Gordian Knot in Preclinical Drug Development
Schäfer-Korting M et al. How Qualification of 3D Disease Models Cuts the Gordian Knot in Preclinical Drug Development. . 2021-00-00. Pubmed ID: 32894342; DOI: 10.1007/164_2020_374 KCLi001-A 2021-00-00 2021-00-00 PubMed: 32894342 DOI: 10.1007/164_2020_374Associated cell lines:
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Kee TR, Espinoza Gonzalez P, Wehinger JL, Bukhari MZ, Ermekbaeva A, Sista A, Kotsiviras P, Liu T, Kang DE, Woo JA
Mitochondrial CHCHD2: Disease-Associated Mutations, Physiological Functions, and Current Animal Models
Kee TR et al. Mitochondrial CHCHD2: Disease-Associated Mutations, Physiological Functions, and Current Animal Models. . 2021-00-00. Pubmed ID: 33967741; DOI: 10.3389/fnagi.2021.660843; PMC: PMC8100248 ZZUi007-A 2021-00-00 2021-00-00 PubMed: 33967741 DOI: 10.3389/fnagi.2021.660843Associated cell lines:
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Yousefi N, Abdollahii S, Kouhbanani MAJ, Hassanzadeh A
Induced pluripotent stem cells (iPSCs) as game-changing tools in the treatment of neurodegenerative disease: Mirage or reality?
Yousefi N et al. Induced pluripotent stem cells (iPSCs) as game-changing tools in the treatment of neurodegenerative disease: Mirage or reality?. . 2020-12-00. Pubmed ID: 32437029; DOI: 10.1002/jcp.29800 IRMBi001-AZZUi003-AZZUi007-AZZUi010-ACSSi002-ACSSi004-AICGi007-ANUIGi043-ANUIGi043-BNUIGi043-CNUIGi044-ANUIGi044-BNUIGi044-CICGi014-A 2020-12-00 2020-12-00 PubMed: 32437029 DOI: 10.1002/jcp.29800Associated cell lines:
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Bahmad HF, Elajami MK, Daouk R, Jalloul H, Darwish B, Chalhoub RM, Assi S, Chamaa F, Abou-Kheir W
Stem Cells: In Sickness and in Health
Bahmad HF et al. Stem Cells: In Sickness and in Health. . 2021-00-00. Pubmed ID: 32867660; DOI: 10.2174/1574888x15999200831160710 IBPi002-A 2021-00-00 2021-00-00 PubMed: 32867660 DOI: 10.2174/1574888x15999200831160710Associated cell lines:
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Liang Y, Liang B, Wu XR, Chen W, Zhao LZ
Network Pharmacology-Based Systematic Analysis of Molecular Mechanisms of Dingji Fumai Decoction for Ventricular Arrhythmia
Liang Y et al. Network Pharmacology-Based Systematic Analysis of Molecular Mechanisms of Dingji Fumai Decoction for Ventricular Arrhythmia. . 2021-00-00. Pubmed ID: 34046076; DOI: 10.1155/2021/5535480; PMC: PMC8128550 NUIGi003-A 2021-00-00 2021-00-00 PubMed: 34046076 DOI: 10.1155/2021/5535480Associated cell lines:
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Bose B, Kapoor S, Nihad M
Induced Pluripotent Stem Cell Derived Human Lung Organoids to Map and Treat the SARS-CoV2 Infections In Vitro
Bose B et al. Induced Pluripotent Stem Cell Derived Human Lung Organoids to Map and Treat the SARS-CoV2 Infections In Vitro. . 2021-00-00. Pubmed ID: 33385178; DOI: 10.1007/5584_2020_613 CSSi001-ANIMHi001-A 2021-00-00 2021-00-00 PubMed: 33385178 DOI: 10.1007/5584_2020_613Associated cell lines:
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Fralish Z, Lotz EM, Chavez T, Khodabukus A, Bursac N
Neuromuscular Development and Disease: Learning From in vitro and in vivo Models
Fralish Z et al. Neuromuscular Development and Disease: Learning From in vitro and in vivo Models. . 2021-00-00. Pubmed ID: 34778273; DOI: 10.3389/fcell.2021.764732; PMC: PMC8579029 CHUQi001-A 2021-00-00 2021-00-00 PubMed: 34778273 DOI: 10.3389/fcell.2021.764732Associated cell lines:
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de Leeuw VC, van Oostrom CTM, Imholz S, Piersma AH, Hessel EVS, Dollé MET
Going Back and Forth: Episomal Vector Reprogramming of Peripheral Blood Mononuclear Cells to Induced Pluripotent Stem Cells and Subsequent Differentiation into Cardiomyocytes and Neuron-Astrocyte Co-cultures
de Leeuw VC et al. Going Back and Forth: Episomal Vector Reprogramming of Peripheral Blood Mononuclear Cells to Induced Pluripotent Stem Cells and Subsequent Differentiation into Cardiomyocytes and Neuron-Astrocyte Co-cultures. . 2020-12-00. Pubmed ID: 33146557; DOI: 10.1089/cell.2020.0040; PMC: PMC7757589 TUSMi005-AFAMRCi006-AFAMRCi006-BICGi014-A 2020-12-00 2020-12-00 PubMed: 33146557 DOI: 10.1089/cell.2020.0040Associated cell lines:
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Yang J, Argenziano MA, Burgos Angulo M, Bertalovitz A, Beidokhti MN, McDonald TV
Phenotypic Variability in iPSC-Induced Cardiomyocytes and Cardiac Fibroblasts Carrying Diverse LMNA Mutations
Yang J et al. Phenotypic Variability in iPSC-Induced Cardiomyocytes and Cardiac Fibroblasts Carrying Diverse LMNA Mutations. . 2021-00-00. Pubmed ID: 34975533; DOI: 10.3389/fphys.2021.778982; PMC: PMC8716763 USFi001-AUSFi002-AUSFi003-AUSFi004-A 2021-00-00 2021-00-00 PubMed: 34975533 DOI: 10.3389/fphys.2021.778982 -
Cheng F, De Luca A, Hogan AL, Rayner SL, Davidson JM, Watchon M, Stevens CH, Muñoz SS, Ooi L, Yerbury JJ, Don EK, Fifita JA, Villalva MD, Suddull H, Chapman TR, Hedl TJ, Walker AK, Yang S, Morsch M, Shi B, Blair IP, Laird AS, Chung RS, Lee A
Unbiased Label-Free Quantitative Proteomics of Cells Expressing Amyotrophic Lateral Sclerosis (ALS) Mutations in CCNF Reveals Activation of the Apoptosis Pathway: A Workflow to Screen Pathogenic Gene Mutations
Cheng F et al. Unbiased Label-Free Quantitative Proteomics of Cells Expressing Amyotrophic Lateral Sclerosis (ALS) Mutations in CCNF Reveals Activation of the Apoptosis Pathway: A Workflow to Screen Pathogenic Gene Mutations. . 2021-00-00. Pubmed ID: 33986643; DOI: 10.3389/fnmol.2021.627740; PMC: PMC8111008 UOWi005-A 2021-00-00 2021-00-00 PubMed: 33986643 DOI: 10.3389/fnmol.2021.627740Associated cell lines:
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Kawase E, Takada K, Suemori H
Kyoto hESC cell resource for regenerative medicine
Kawase E et al. Kyoto hESC cell resource for regenerative medicine. . 2020-12-00. Pubmed ID: 33059130; DOI: 10.1016/j.scr.2020.102020 KUIMSe001-AKUIMSe002-AKUIMSe003-AKUIMSe004-AKUIMSe005-AKUIMSe006-AKUIMSe007-A 2020-12-00 2020-12-00 PubMed: 33059130 DOI: 10.1016/j.scr.2020.102020Associated cell lines:
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Lin HY, Ou-Yang CH, Lin CH
Reprogramming of a human induced pluripotent stem cell (iPSC) line from a patient with neurodegeneration with brain iron accumulation (NBIA) harboring a novel frameshift mutation in C19orf12 gene
Lin HY et al. Reprogramming of a human induced pluripotent stem cell (iPSC) line from a patient with neurodegeneration with brain iron accumulation (NBIA) harboring a novel frameshift mutation in C19orf12 gene. . 2020-12-00. Pubmed ID: 33068888; DOI: 10.1016/j.scr.2020.102032 IBMSi024-A 2020-12-00 2020-12-00 PubMed: 33068888 DOI: 10.1016/j.scr.2020.102032Associated cell lines:
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Yao L, Wu J, Koc S, Lu G
Genetic Imaging of Neuroinflammation in Parkinson's Disease: Recent Advancements
Yao L et al. Genetic Imaging of Neuroinflammation in Parkinson's Disease: Recent Advancements. . 2021-00-00. Pubmed ID: 34336822; DOI: 10.3389/fcell.2021.655819; PMC: PMC8320775 GIBHi004-A 2021-00-00 2021-00-00 PubMed: 34336822 DOI: 10.3389/fcell.2021.655819Associated cell lines:
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Tahbaz M, Yoshihara E
Immune Protection of Stem Cell-Derived Islet Cell Therapy for Treating Diabetes
Tahbaz M et al. Immune Protection of Stem Cell-Derived Islet Cell Therapy for Treating Diabetes. . 2021-00-00. Pubmed ID: 34447354; DOI: 10.3389/fendo.2021.716625; PMC: PMC8382875 USTCi001-AUSTCi001-A-1 2021-00-00 2021-00-00 PubMed: 34447354 DOI: 10.3389/fendo.2021.716625Associated cell lines:
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Hage R, Vignal-Clermont C
Leber Hereditary Optic Neuropathy: Review of Treatment and Management
Hage R et al. Leber Hereditary Optic Neuropathy: Review of Treatment and Management. . 2021-00-00. Pubmed ID: 34122299; DOI: 10.3389/fneur.2021.651639; PMC: PMC8187781 FINCBi001-A 2021-00-00 2021-00-00 PubMed: 34122299 DOI: 10.3389/fneur.2021.651639Associated cell lines:
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Kantor Boris, Chiba-Falek Ornit
Lentiviral vectors as the delivery vehicles for transduction into iPSCs
Kantor Boris et al. Lentiviral vectors as the delivery vehicles for transduction into iPSCs. . 2021-00-00. DOI: 10.1016/b978-0-323-85766-6.00005-x ICGi015-AICGi015-B 2021-00-00 2021-00-00 DOI: 10.1016/b978-0-323-85766-6.00005-x -
Khorkova O, Hsiao J, Wahlestedt C
Nucleic Acid-Based Therapeutics in Orphan Neurological Disorders: Recent Developments
Khorkova O et al. Nucleic Acid-Based Therapeutics in Orphan Neurological Disorders: Recent Developments. . 2021-00-00. Pubmed ID: 33996898; DOI: 10.3389/fmolb.2021.643681; PMC: PMC8115123 USTCi001-AUSTCi001-A-1 2021-00-00 2021-00-00 PubMed: 33996898 DOI: 10.3389/fmolb.2021.643681Associated cell lines:
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Rattananon P, Anurathapan U, Bhukhai K, Hongeng S
The Future of Gene Therapy for Transfusion-Dependent Beta-Thalassemia: The Power of the Lentiviral Vector for Genetically Modified Hematopoietic Stem Cells
Rattananon P et al. The Future of Gene Therapy for Transfusion-Dependent Beta-Thalassemia: The Power of the Lentiviral Vector for Genetically Modified Hematopoietic Stem Cells. . 2021-00-00. Pubmed ID: 34658870; DOI: 10.3389/fphar.2021.730873; PMC: PMC8517149 MUi009-A 2021-00-00 2021-00-00 PubMed: 34658870 DOI: 10.3389/fphar.2021.730873Associated cell lines:
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Ovchinnikov Dmitry A.
Genetically-modified cell lines: categorisation and considerations for characterisation
Ovchinnikov Dmitry A.. Genetically-modified cell lines: categorisation and considerations for characterisation. . 2020-12-00. DOI: 10.1016/j.scr.2020.102103 AIBNe001-A 2020-12-00 2020-12-00 DOI: 10.1016/j.scr.2020.102103Associated cell lines:
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Santos HS, Poletto E, Schuh R, Matte U, Baldo G
Genome editing in mucopolysaccharidoses and mucolipidoses
Santos HS et al. Genome editing in mucopolysaccharidoses and mucolipidoses. . 2021-00-00. Pubmed ID: 34175047; DOI: 10.1016/bs.pmbts.2021.01.026 TRNDi005-ABRCi001-ATRNDi006-A 2021-00-00 2021-00-00 PubMed: 34175047 DOI: 10.1016/bs.pmbts.2021.01.026Associated cell lines:
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Hu B, Duan S, Wang Z, Li X, Zhou Y, Zhang X, Zhang YW, Xu H, Zheng H
Insights Into the Role of CSF1R in the Central Nervous System and Neurological Disorders
Hu B et al. Insights Into the Role of CSF1R in the Central Nervous System and Neurological Disorders. . 2021-00-00. Pubmed ID: 34867307; DOI: 10.3389/fnagi.2021.789834; PMC: PMC8634759 HIHCNi003-A 2021-00-00 2021-00-00 PubMed: 34867307 DOI: 10.3389/fnagi.2021.789834Associated cell lines:
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Inglés-Ferrándiz M, Martin-Inaraja M, Herrera L, Villaverde M, Santos S, Vesga MA, Garreta E, Martín-Ruiz I, Aransay AM, Anguita J, Barreña B, Allende LM, Gonzalez-Granado LI, Eguizabal C
Generation, establishment and characterization of a pluripotent stem cell line (CVTTHi001-A) from primary fibroblasts isolated from a patient with activated PI3 kinase delta syndrome (APDS2)
Inglés-Ferrándiz M et al. Generation, establishment and characterization of a pluripotent stem cell line (CVTTHi001-A) from primary fibroblasts isolated from a patient with activated PI3 kinase delta syndrome (APDS2). . 2020-12-00. Pubmed ID: 33221676; DOI: 10.1016/j.scr.2020.102082 CVTTHi001-A 2020-12-00 2020-12-00 PubMed: 33221676 DOI: 10.1016/j.scr.2020.102082Associated cell lines:
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Jiang P, Iqbal A, Wang M, Li X, Fang X, Yu H, Zhao Z
Transcriptomic Analysis of Short/Branched-Chain Acyl-Coenzyme a Dehydrogenase Knocked Out bMECs Revealed Its Regulatory Effect on Lipid Metabolism
Jiang P et al. Transcriptomic Analysis of Short/Branched-Chain Acyl-Coenzyme a Dehydrogenase Knocked Out bMECs Revealed Its Regulatory Effect on Lipid Metabolism. . 2021-00-00. Pubmed ID: 34557544; DOI: 10.3389/fvets.2021.744287; PMC: PMC8453006 WAe009-AWAe009-A-16 2021-00-00 2021-00-00 PubMed: 34557544 DOI: 10.3389/fvets.2021.744287Associated cell lines:
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Peng S, Chen M, Yin M, Feng H
Identifying the Potential Therapeutic Targets for Atopic Dermatitis Through the Immune Infiltration Analysis and Construction of a ceRNA Network
Peng S et al. Identifying the Potential Therapeutic Targets for Atopic Dermatitis Through the Immune Infiltration Analysis and Construction of a ceRNA Network. . 2021-00-00. Pubmed ID: 33994801; DOI: 10.2147/ccid.s310426; PMC: PMC8112859 CIBi008-A 2021-00-00 2021-00-00 PubMed: 33994801 DOI: 10.2147/ccid.s310426Associated cell lines:
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Mallach A, Gobom J, Zetterberg H, Hardy J, Piers TM, Wray S, Pocock JM
The influence of the R47H triggering receptor expressed on myeloid cells 2 variant on microglial exosome profiles
Mallach A et al. The influence of the R47H triggering receptor expressed on myeloid cells 2 variant on microglial exosome profiles. . 2021-00-00. Pubmed ID: 34704019; DOI: 10.1093/braincomms/fcab009; PMC: PMC8244649 BIONi010-C 2021-00-00 2021-00-00 PubMed: 34704019 DOI: 10.1093/braincomms/fcab009Associated cell lines:
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De Sousa Paul A.
Human Embryonic Stem Cell Banking for Clinical Applications—20 Years from Their Isolation
De Sousa Paul A.. Human Embryonic Stem Cell Banking for Clinical Applications—20 Years from Their Isolation. . 2021-00-00. DOI: 10.1007/978-3-030-71621-9_15 RCe013-ARCe015-ARCe016-ARCe017-ARCe019-ARCe020-ARCe021-A 2021-00-00 2021-00-00 DOI: 10.1007/978-3-030-71621-9_15 -
Shaker MR, Pietrogrande G, Martin S, Lee JH, Sun W, Wolvetang EJ
Rapid and Efficient Generation of Myelinating Human Oligodendrocytes in Organoids
Shaker MR et al. Rapid and Efficient Generation of Myelinating Human Oligodendrocytes in Organoids. . 2021-00-00. Pubmed ID: 33815061; DOI: 10.3389/fncel.2021.631548; PMC: PMC8010307 UCSFi001-A 2021-00-00 2021-00-00 PubMed: 33815061 DOI: 10.3389/fncel.2021.631548Associated cell lines:
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Chahine Mohamed
Lymphoblastoid-derived human-induced pluripotent stem cells
Chahine Mohamed. Lymphoblastoid-derived human-induced pluripotent stem cells. . 2021-00-00. DOI: 10.1016/b978-0-12-822135-8.00005-7 CHUQi001-ATUSMi001-A 2021-00-00 2021-00-00 DOI: 10.1016/b978-0-12-822135-8.00005-7Associated cell lines:
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Astro V, Alowaysi M, Fiacco E, Saera-Vila A, Cardona-Londoño KJ, Aiese Cigliano R, Adamo A
Pseudoautosomal Region 1 Overdosage Affects the Global Transcriptome in iPSCs From Patients With Klinefelter Syndrome and High-Grade X Chromosome Aneuploidies
Astro V et al. Pseudoautosomal Region 1 Overdosage Affects the Global Transcriptome in iPSCs From Patients With Klinefelter Syndrome and High-Grade X Chromosome Aneuploidies. . 2021-00-00. Pubmed ID: 35186953; DOI: 10.3389/fcell.2021.801597; PMC: PMC8850648 KAUSTi001-AKAUSTi003-AKAUSTi004-AKAUSTi004-BKAUSTi005-AKAUSTi005-BKAUSTi005-CKAUSTi001-BKAUSTi006-AKAUSTi006-BKAUSTi007-AKAUSTi008-AKAUSTi008-BKAUSTi008-CKAUSTi008-DKAUSTi008-EKAUSTi008-FKAUSTi008-GKAUSTi007-BKAUSTi009-AKAUSTi009-BKAUSTi010-AKAUSTi010-B 2021-00-00 2021-00-00 PubMed: 35186953 DOI: 10.3389/fcell.2021.801597 -
Pulimamidi Vinay Kumar, Maddileti Savitri, Mariappan Indumathi
Induced pluripotent stem-cell-derived corneal grafts and organoids
Pulimamidi Vinay Kumar et al. Induced pluripotent stem-cell-derived corneal grafts and organoids. . 2021-00-00. DOI: 10.1016/b978-0-12-823809-7.00005-0 HMUi001-A 2021-00-00 2021-00-00 DOI: 10.1016/b978-0-12-823809-7.00005-0Associated cell lines:
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Li S, Ding C, Guo Y, Zhang Y, Wang H, Sun X, Zhang J, Cui Z, Chen J
Mechanotransduction Regulates Reprogramming Enhancement in Adherent 3D Keratocyte Cultures
Li S et al. Mechanotransduction Regulates Reprogramming Enhancement in Adherent 3D Keratocyte Cultures. . 2021-00-00. Pubmed ID: 34568299; DOI: 10.3389/fbioe.2021.709488; PMC: PMC8460903 HMUi001-A 2021-00-00 2021-00-00 PubMed: 34568299 DOI: 10.3389/fbioe.2021.709488Associated cell lines:
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Zouboulis CC, Makrantonaki E, Hossini AM
Skin Mirrors Brain: A Chance for Alzheimer's Disease Research
Zouboulis CC et al. Skin Mirrors Brain: A Chance for Alzheimer's Disease Research. . 2021-00-00. Pubmed ID: 35023127; DOI: 10.1007/978-3-030-78787-5_45 IRMBi001-AIRMBi002-AZZUi009-AICGi008-AICGi008-BICCSICi007-A 2021-00-00 2021-00-00 PubMed: 35023127 DOI: 10.1007/978-3-030-78787-5_45Associated cell lines:
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Valadez-Barba V, Cota-Coronado A, Hernández-Pérez OR, Lugo-Fabres PH, Padilla-Camberos E, Díaz NF, Díaz-Martínez NE
iPSC for modeling neurodegenerative disorders
Valadez-Barba V et al. iPSC for modeling neurodegenerative disorders. . 2020-12-00. Pubmed ID: 33426236; DOI: 10.1016/j.reth.2020.11.006; PMC: PMC7770414 IPTi005-AIPTi007-AUNIGEi003-A 2020-12-00 2020-12-00 PubMed: 33426236 DOI: 10.1016/j.reth.2020.11.006Associated cell lines:
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Wang X, Gao C, Zhang Y, Hu S, Qiao Y, Zhao Z, Gou L, Song J, Wang Q
Overexpression of mGluR7 in the Prefrontal Cortex Attenuates Autistic Behaviors in Mice
Wang X et al. Overexpression of mGluR7 in the Prefrontal Cortex Attenuates Autistic Behaviors in Mice. . 2021-00-00. Pubmed ID: 34335187; DOI: 10.3389/fncel.2021.689611; PMC: PMC8319395 SDQLCHi014-A 2021-00-00 2021-00-00 PubMed: 34335187 DOI: 10.3389/fncel.2021.689611Associated cell lines:
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Heller S, Melzer MK, Azoitei N, Julier C, Kleger A
Human Pluripotent Stem Cells Go Diabetic: A Glimpse on Monogenic Variants
Heller S et al. Human Pluripotent Stem Cells Go Diabetic: A Glimpse on Monogenic Variants. . 2021-00-00. Pubmed ID: 34079523; DOI: 10.3389/fendo.2021.648284; PMC: PMC8166226 QBRIi007-A 2021-00-00 2021-00-00 PubMed: 34079523 DOI: 10.3389/fendo.2021.648284Associated cell lines:
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Jiang X, Chen Y, Liu X, Ye L, Yu M, Shen Z, Lei W, Hu S
Uncovering Inherited Cardiomyopathy With Human Induced Pluripotent Stem Cells
Jiang X et al. Uncovering Inherited Cardiomyopathy With Human Induced Pluripotent Stem Cells. . 2021-00-00. Pubmed ID: 34079803; DOI: 10.3389/fcell.2021.672039; PMC: PMC8166268 ZZUNEUi020-ASCVIi003-ASCVIi004-ASCVIi005-A 2021-00-00 2021-00-00 PubMed: 34079803 DOI: 10.3389/fcell.2021.672039Associated cell lines:
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Deinsberger Julia, Weber Benedikt
Induced pluripotent stem cells for vascular tissue engineering
Deinsberger Julia et al. Induced pluripotent stem cells for vascular tissue engineering. . 2021-00-00. DOI: 10.1016/b978-0-12-823809-7.00002-5 ICGi015-AICGi015-B 2021-00-00 2021-00-00 DOI: 10.1016/b978-0-12-823809-7.00002-5 -
Lu K, Seidel T, Cao-Ehlker X, Dorn T, Batcha AMN, Schneider CM, Semmler M, Volk T, Moretti A, Dendorfer A, Tomasi R
Progressive stretch enhances growth and maturation of 3D stem-cell-derived myocardium
Lu K et al. Progressive stretch enhances growth and maturation of 3D stem-cell-derived myocardium. . 2021-00-00. Pubmed ID: 33995650; DOI: 10.7150/thno.54999; PMC: PMC8120210 MRIi004-A 2021-00-00 2021-00-00 PubMed: 33995650 DOI: 10.7150/thno.54999Associated cell lines:
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Donada A, Basso-Valentina F, Arkoun B, Monte-Mor B, Plo I, Raslova H
Induced pluripotent stem cells and hematological malignancies: A powerful tool for disease modeling and drug development
Donada A et al. Induced pluripotent stem cells and hematological malignancies: A powerful tool for disease modeling and drug development. . 2020-12-00. Pubmed ID: 33142254; DOI: 10.1016/j.scr.2020.102060 CHOPi001-A 2020-12-00 2020-12-00 PubMed: 33142254 DOI: 10.1016/j.scr.2020.102060Associated cell lines:
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Zheng Y, Cai B, Ren C, Xu H, Du W, Wu Y, Lin F, Zhang H, Quan R
Identification of immune related cells and crucial genes in the peripheral blood of ankylosing spondylitis by integrated bioinformatics analysis
Zheng Y et al. Identification of immune related cells and crucial genes in the peripheral blood of ankylosing spondylitis by integrated bioinformatics analysis. . 2021-00-00. Pubmed ID: 34589304; DOI: 10.7717/peerj.12125; PMC: PMC8432305 XDCMHi001-A 2021-00-00 2021-00-00 PubMed: 34589304 DOI: 10.7717/peerj.12125Associated cell lines:
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Ucuncu E, Rajamani K, Wilson MSC, Medina-Cano D, Altin N, David P, Barcia G, Lefort N, Banal C, Vasilache-Dangles MT, Pitelet G, Lorino E, Rabasse N, Bieth E, Zaki MS, Topcu M, Sonmez FM, Musaev D, Stanley V, Bole-Feysot C, Nitschké P, Munnich A, Bahi-Buisson N, Fossoud C, Giuliano F, Colleaux L, Burglen L, Gleeson JG, Boddaert N, Saiardi A, Cantagrel V
MINPP1 prevents intracellular accumulation of the chelator inositol hexakisphosphate and is mutated in Pontocerebellar Hypoplasia
Ucuncu E et al. MINPP1 prevents intracellular accumulation of the chelator inositol hexakisphosphate and is mutated in Pontocerebellar Hypoplasia. . 2020-11-30. Pubmed ID: 33257696; DOI: 10.1038/s41467-020-19919-y; PMC: PMC7705663 IMAGINi004-A 2020-11-30 2020-11-30 PubMed: 33257696 DOI: 10.1038/s41467-020-19919-yAssociated cell lines:
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Grinkevich L.N.
Леонид Валентинович Розенштраух 10 апреля 1937–18 сентября 2020 г.
Grinkevich L.N.. Леонид Валентинович Розенштраух 10 апреля 1937–18 сентября 2020 г. . 2021-00-00. DOI: 10.31857/s0301179821030061 ICGi018-A 2021-00-00 2021-00-00 DOI: 10.31857/s0301179821030061Associated cell lines:
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Ji X, Tang Q, Tang C, Wu Z, Ma L, Guo X, Cheng G, Chen Y, Yang T, Xiong M, Zhou W
Generation of an induced pluripotent stem cell line from an Alström Syndrome patient with ALMS1 mutation (c.3902C > A, c.6436C > T) and a gene correction isogenic iPSC line
Ji X et al. Generation of an induced pluripotent stem cell line from an Alström Syndrome patient with ALMS1 mutation (c.3902C > A, c.6436C > T) and a gene correction isogenic iPSC line. . 2020-12-00. Pubmed ID: 33264725; DOI: 10.1016/j.scr.2020.102089 FDCHi003-AFDCHi003-A-1 2020-12-00 2020-12-00 PubMed: 33264725 DOI: 10.1016/j.scr.2020.102089Associated cell lines:
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Méjécase C, Harding P, Sarkar H, Eintracht J, Lima Cunha D, Toualbi L, Moosajee M
Generation of two human control iPS cell lines (UCLi016-A and UCLi017-A) from healthy donors with no known ocular conditions
Méjécase C et al. Generation of two human control iPS cell lines (UCLi016-A and UCLi017-A) from healthy donors with no known ocular conditions. . 2020-12-00. Pubmed ID: 33370878; DOI: 10.1016/j.scr.2020.102113; PMC: PMC7768179 UCLi016-AUCLi017-A 2020-12-00 2020-12-00 PubMed: 33370878 DOI: 10.1016/j.scr.2020.102113 -
Datta I, Jagtap S, Sowmithra, Yadav R, Pal PK
Generation of induced pluripotent stem cells (NIMHi002-A and NIMHi003-A) from two sporadic Parkinson's disease patient of East Indian ethnicity
Datta I et al. Generation of induced pluripotent stem cells (NIMHi002-A and NIMHi003-A) from two sporadic Parkinson's disease patient of East Indian ethnicity. . 2020-12-00. Pubmed ID: 33010678; DOI: 10.1016/j.scr.2020.101995 HEBHMUi001-ANIMHi001-ANIMHi002-ANIMHi003-A 2020-12-00 2020-12-00 PubMed: 33010678 DOI: 10.1016/j.scr.2020.101995Associated cell lines:
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Zhou Y, Cui Z, Jing Y, Mao S, Chen D, Ding C, Gu J, Chan HF, Tang S, Chen J
Establishment of non-integrate induced pluripotent stem cell line CSUASOi006-A, from urine-derived cells of a PRPF8-related dominant retinitis pigmentosa patient
Zhou Y et al. Establishment of non-integrate induced pluripotent stem cell line CSUASOi006-A, from urine-derived cells of a PRPF8-related dominant retinitis pigmentosa patient. . 2020-12-00. Pubmed ID: 33157387; DOI: 10.1016/j.scr.2020.102041 CSUASOi006-A 2020-12-00 2020-12-00 PubMed: 33157387 DOI: 10.1016/j.scr.2020.102041Associated cell lines:
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Su J, Wang J, Wang L, Li T, Wang H, Shen J, Wang H, Zhang J, Lin W, Huang J, Liang P
Generation of five induced pluripotent stem cell lines with DMD/c.497G > T mutation from renal epithelial cells of a Duchenne muscular dystrophy patient and a recessive carrier parent
Su J et al. Generation of five induced pluripotent stem cell lines with DMD/c.497G > T mutation from renal epithelial cells of a Duchenne muscular dystrophy patient and a recessive carrier parent. . 2020-12-00. Pubmed ID: 33039804; DOI: 10.1016/j.scr.2020.102021 ZJUi001-AZJUi001-BZJUi001-CZJUi002-AZJUi002-BZJUi002-C 2020-12-00 2020-12-00 PubMed: 33039804 DOI: 10.1016/j.scr.2020.102021 -
Ou-Yang CH, Lin HY, Huang CY, Lin CH
Generation of a human induced pluripotent stem cell (iPSC) line (IBMS-iPSC-057-05) from a patient with familial parkinsonism and polyneuropathy having a heterozygous p.Y314S mutation in UQCRC1 gene
Ou-Yang CH et al. Generation of a human induced pluripotent stem cell (iPSC) line (IBMS-iPSC-057-05) from a patient with familial parkinsonism and polyneuropathy having a heterozygous p.Y314S mutation in UQCRC1 gene. . 2020-12-00. Pubmed ID: 33070102; DOI: 10.1016/j.scr.2020.102031 IBMSi022-A 2020-12-00 2020-12-00 PubMed: 33070102 DOI: 10.1016/j.scr.2020.102031Associated cell lines:
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Franz M, Hagenau L, Koch R, Neubauer S, Nowack B, Tzvetkova A, Jensen LR, Kuss AW
Generation of an iPSC line (UMGWi001-B) from a patient with Floating-Harbor Syndrome (FLHS) carrying a heterozygous SRCAP mutation (p.Arg2444)
Franz M et al. Generation of an iPSC line (UMGWi001-B) from a patient with Floating-Harbor Syndrome (FLHS) carrying a heterozygous SRCAP mutation (p.Arg2444). . 2020-12-00. Pubmed ID: 33099107; DOI: 10.1016/j.scr.2020.102028 UMGWi001-B 2020-12-00 2020-12-00 PubMed: 33099107 DOI: 10.1016/j.scr.2020.102028Associated cell lines:
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Cerrada V, García-López M, Alvarez-Galeano S, Moreno-Izquierdo A, Lucia A, Rabasa Pérez M, Arenas J, Gallardo ME
Generation of the iPSC line IISHDOi007-A from peripheral blood mononuclear cells from a patient with McArdle disease harbouring the mutation c.2392 T > C; p.Trp798Arg
Cerrada V et al. Generation of the iPSC line IISHDOi007-A from peripheral blood mononuclear cells from a patient with McArdle disease harbouring the mutation c.2392 T > C; p.Trp798Arg. . 2020-12-00. Pubmed ID: 33370875; DOI: 10.1016/j.scr.2020.102108 IISHDOi007-A 2020-12-00 2020-12-00 PubMed: 33370875 DOI: 10.1016/j.scr.2020.102108Associated cell lines:
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Alowaysi M, Fiacco E, Astro V, Adamo A
Establishment of iPSC lines from a high-grade Klinefelter Syndrome patient (49-XXXXY) and two genetically matched healthy relatives (KAUSTi003-A, KAUSTi004-A, KAUSTi004-B, KAUSTi005-A, KAUSTi005-B, KAUSTi005-C)
Alowaysi M et al. Establishment of iPSC lines from a high-grade Klinefelter Syndrome patient (49-XXXXY) and two genetically matched healthy relatives (KAUSTi003-A, KAUSTi004-A, KAUSTi004-B, KAUSTi005-A, KAUSTi005-B, KAUSTi005-C). . 2020-12-00. Pubmed ID: 32987351; DOI: 10.1016/j.scr.2020.102008 KAUSTi003-AKAUSTi004-AKAUSTi004-BKAUSTi005-AKAUSTi005-BKAUSTi005-C 2020-12-00 2020-12-00 PubMed: 32987351 DOI: 10.1016/j.scr.2020.102008Associated cell lines:
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Kuebler B, Aran B, Flores R, Pérez-Jurado LA, Veiga A, Corominas R, Cuscó I
Generation of induced pluripotent stem cells (iPSCs) by retroviral transduction of skin fibroblasts from four patients suffering Williams-Beuren syndrome (7q11.23 deletion)
Kuebler B et al. Generation of induced pluripotent stem cells (iPSCs) by retroviral transduction of skin fibroblasts from four patients suffering Williams-Beuren syndrome (7q11.23 deletion). . 2020-12-00. Pubmed ID: 33370870; DOI: 10.1016/j.scr.2020.102087 ESi059-AESi060-BESi068-AESi069-A 2020-12-00 2020-12-00 PubMed: 33370870 DOI: 10.1016/j.scr.2020.102087 -
Khabarova AA, Pristyazhnyuk IE, Orlova PA, Nikitina TV, Kashevarova AA, Lopatkina ME, Belyaeva EO, Sukhanova NN, Nazarenko LP, Lebedev IN, Serov OL
Generation of iPSC line ICGi024-A from human skin fibroblasts of a patient with ring chromosome 18
Khabarova AA et al. Generation of iPSC line ICGi024-A from human skin fibroblasts of a patient with ring chromosome 18. . 2020-12-00. Pubmed ID: 33212351; DOI: 10.1016/j.scr.2020.102076 ICGi016-AICGi024-A 2020-12-00 2020-12-00 PubMed: 33212351 DOI: 10.1016/j.scr.2020.102076 -
Cristian FB, Köppel A, Janssen J, Utikal JS, Rappold GA, Berkel S
Generation of two hiPSC lines from a patient with autism spectrum disorder harboring a 120 kb deletion in SHANK2 and two control lines from each parent
Cristian FB et al. Generation of two hiPSC lines from a patient with autism spectrum disorder harboring a 120 kb deletion in SHANK2 and two control lines from each parent. . 2020-12-00. Pubmed ID: 33002717; DOI: 10.1016/j.scr.2020.102004 UKHGi001-AUKHGi001-BUKHGi002-AUKHGi002-BUKHGi003-AUKHGi003-B 2020-12-00 2020-12-00 PubMed: 33002717 DOI: 10.1016/j.scr.2020.102004Associated cell lines:
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Völkner C, Liedtke M, Petters J, Huth K, Knuebel G, Murua Escobar H, Bullerdiek J, Lukas J, Hermann A, Frech MJ
Generation of an iPSC line (AKOSi006-A) from fibroblasts of an NPC1 patient, carrying the homozygous mutation p.I1061T (c.3182 T > C) and a control iPSC line (AKOSi007-A) using a non-integrating Sendai virus system
Völkner C et al. Generation of an iPSC line (AKOSi006-A) from fibroblasts of an NPC1 patient, carrying the homozygous mutation p.I1061T (c.3182 T > C) and a control iPSC line (AKOSi007-A) using a non-integrating Sendai virus system. . 2020-12-00. Pubmed ID: 33099109; DOI: 10.1016/j.scr.2020.102056 AKOSi006-AAKOSi007-A 2020-12-00 2020-12-00 PubMed: 33099109 DOI: 10.1016/j.scr.2020.102056Associated cell lines:
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Sar P, Dalai S
CRISPR/Cas9 in epigenetics studies of health and disease
Sar P et al. CRISPR/Cas9 in epigenetics studies of health and disease. . 2021-00-00. Pubmed ID: 34127198; DOI: 10.1016/bs.pmbts.2021.01.022 CSSi002-A 2021-00-00 2021-00-00 PubMed: 34127198 DOI: 10.1016/bs.pmbts.2021.01.022Associated cell lines:
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Dimai S, Semmler L, Prabhu A, Stachelscheid H, Huettemeister J, Klaucke SC, Lacour P, Blaschke F, Kruse J, Parwani A, Boldt LH, Bullinger L, Pieske BM, Heinzel FR, Hohendanner F
COVID19-associated cardiomyocyte dysfunction, arrhythmias and the effect of Canakinumab
Dimai S et al. COVID19-associated cardiomyocyte dysfunction, arrhythmias and the effect of Canakinumab. . 2021-00-00. Pubmed ID: 34411149; DOI: 10.1371/journal.pone.0255976; PMC: PMC8376065 BIHi004-A 2021-00-00 2021-00-00 PubMed: 34411149 DOI: 10.1371/journal.pone.0255976Associated cell lines:
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Fieldes M, Ahmed E, Bourguignon C, Mianné J, Martin M, Arnould C, Vachier I, Assou S, De Vos J, Bourdin A
Generation of the induced pluripotent stem cell line UHOMi002-A from peripheral blood mononuclear cells of a healthy male donor
Fieldes M et al. Generation of the induced pluripotent stem cell line UHOMi002-A from peripheral blood mononuclear cells of a healthy male donor. . 2020-12-00. Pubmed ID: 33099111; DOI: 10.1016/j.scr.2020.102037 UHOMi001-AUHOMi002-A 2020-12-00 2020-12-00 PubMed: 33099111 DOI: 10.1016/j.scr.2020.102037Associated cell lines:
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Yamasaki AE, Warshaw JN, Kyalwazi BL, Matsui H, Jepsen K, Panopoulos AD
An iPSC line derived from a human acute myeloid leukemia cell line (HL-60-iPSC) retains leukemic abnormalities and displays myeloid differentiation defects
Yamasaki AE et al. An iPSC line derived from a human acute myeloid leukemia cell line (HL-60-iPSC) retains leukemic abnormalities and displays myeloid differentiation defects. . 2020-12-00. Pubmed ID: 33370871; DOI: 10.1016/j.scr.2020.102096; PMC: PMC8031422 NDi001-A 2020-12-00 2020-12-00 PubMed: 33370871 DOI: 10.1016/j.scr.2020.102096Associated cell lines:
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Szabó E, Reé D, Jezsó B, Vincze K, Földes G, Molnár AÁ, Réthelyi JM, Apáti Á
Generation of iPSC lines from peripheral blood mononuclear cells of identical twins both suffering from type 2 diabetes mellitus and one of them additionally diagnosed with atherosclerosis
Szabó E et al. Generation of iPSC lines from peripheral blood mononuclear cells of identical twins both suffering from type 2 diabetes mellitus and one of them additionally diagnosed with atherosclerosis. . 2020-12-00. Pubmed ID: 33099106; DOI: 10.1016/j.scr.2020.102051 RCNSi001-ARCNSi001-BRCNSi002-ARCNSi002-B 2020-12-00 2020-12-00 PubMed: 33099106 DOI: 10.1016/j.scr.2020.102051Associated cell lines:
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Scalise S, Scaramuzzino L, Lucchino V, Esposito C, Malatesta P, Grillone K, Perrotti N, Cuda G, Parrotta EI
Generation of iPSC lines from two patients affected by febrile seizure due to inherited missense mutation in SCN1A gene
Scalise S et al. Generation of iPSC lines from two patients affected by febrile seizure due to inherited missense mutation in SCN1A gene. . 2020-12-00. Pubmed ID: 33370868; DOI: 10.1016/j.scr.2020.102083 UNIMGi001-AUNIMGi002-A 2020-12-00 2020-12-00 PubMed: 33370868 DOI: 10.1016/j.scr.2020.102083Associated cell lines:
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Bozaoglu K, Shern Lee W, Haebich KM, North KN, Payne JM, Lockhart PJ
Generation of four iPSC lines from Neurofibromatosis Type 1 patients
Bozaoglu K et al. Generation of four iPSC lines from Neurofibromatosis Type 1 patients. . 2020-12-00. Pubmed ID: 33091851; DOI: 10.1016/j.scr.2020.102013 MCRIi020-AMCRIi021-AMCRIi022-AMCRIi023-A 2020-12-00 2020-12-00 PubMed: 33091851 DOI: 10.1016/j.scr.2020.102013Associated cell lines:
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Bono F, Mutti V, Piovani G, Minelli A, Mingardi J, Guglielmi A, Fiorentini C, Barbon A, Missale C, Gennarelli M
Generation of two human induced pluripotent stem cell lines, UNIBSi012-A and UNIBSi013-A, from two patients with treatment-resistant depression
Bono F et al. Generation of two human induced pluripotent stem cell lines, UNIBSi012-A and UNIBSi013-A, from two patients with treatment-resistant depression. . 2020-12-00. Pubmed ID: 33291010; DOI: 10.1016/j.scr.2020.102104 UNIBSi012-AUNIBSi013-A 2020-12-00 2020-12-00 PubMed: 33291010 DOI: 10.1016/j.scr.2020.102104Associated cell lines:
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Lim SW, Shin YJ, Cui S, Ko EJ, Lee KI, Lee JY, Chung BH, Yang CW
Generation of a human induced pluripotent stem cell line (CMCi002-A) from a patient with Gitelman's syndrome
Lim SW et al. Generation of a human induced pluripotent stem cell line (CMCi002-A) from a patient with Gitelman's syndrome. . 2020-12-00. Pubmed ID: 33370877; DOI: 10.1016/j.scr.2020.102110 CMCi002-A 2020-12-00 2020-12-00 PubMed: 33370877 DOI: 10.1016/j.scr.2020.102110Associated cell lines:
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Schuster J, Hoeber J, Sobol M, Fatima A, Annerén G, Dahl N
Generation of two human iPSC lines (UUIGPi013-A and UUIPGi014-A) from cases with Down syndrome and full trisomy for chromosome 21 (T21)
Schuster J et al. Generation of two human iPSC lines (UUIGPi013-A and UUIPGi014-A) from cases with Down syndrome and full trisomy for chromosome 21 (T21). . 2020-12-00. Pubmed ID: 33220594; DOI: 10.1016/j.scr.2020.102081 UUIGPi013-AUUIGPi014-A 2020-12-00 2020-12-00 PubMed: 33220594 DOI: 10.1016/j.scr.2020.102081Associated cell lines:
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Wang H, Wu K, Guan J, Wang Q
Generation of a human induced pluripotent stem cell line (CPGHi001-A) from a hearing loss patient with the TMC1 p.M418K mutation
Wang H et al. Generation of a human induced pluripotent stem cell line (CPGHi001-A) from a hearing loss patient with the TMC1 p.M418K mutation. . 2020-12-00. Pubmed ID: 33217648; DOI: 10.1016/j.scr.2020.101982 CPGHi001-A 2020-12-00 2020-12-00 PubMed: 33217648 DOI: 10.1016/j.scr.2020.101982Associated cell lines:
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Zhu X, Wang J, Chong H, Wang J, Wang D
Generation of induced pluripotent stem cells (NJDTHi001-A) from a Danon disease child with mutation of c.467 T > G in LAMP2 gene
Zhu X et al. Generation of induced pluripotent stem cells (NJDTHi001-A) from a Danon disease child with mutation of c.467 T > G in LAMP2 gene. . 2020-12-00. Pubmed ID: 33038746; DOI: 10.1016/j.scr.2020.101994 NJDTHi001-A 2020-12-00 2020-12-00 PubMed: 33038746 DOI: 10.1016/j.scr.2020.101994Associated cell lines:
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Wang Z, Cui Y, Shan Y, Kang B, Shi L, Geng K, Han J
Generation of a MCPH1 knockout human embryonic stem cell line by CRISPR/Cas9 technology
Wang Z et al. Generation of a MCPH1 knockout human embryonic stem cell line by CRISPR/Cas9 technology. . 2020-12-00. Pubmed ID: 33370873; DOI: 10.1016/j.scr.2020.102105 WAe001-A-52 2020-12-00 2020-12-00 PubMed: 33370873 DOI: 10.1016/j.scr.2020.102105Associated cell lines:
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Xiao Y, Li J, Qiu L, Jiang C, Huang Y, Liu J, Sun Q, Hong H, Ye L
Dexmedetomidine Protects Human Cardiomyocytes Against Ischemia-Reperfusion Injury Through α2-Adrenergic Receptor/AMPK-Dependent Autophagy
Xiao Y et al. Dexmedetomidine Protects Human Cardiomyocytes Against Ischemia-Reperfusion Injury Through α2-Adrenergic Receptor/AMPK-Dependent Autophagy. . 2021-00-00. Pubmed ID: 34093174; DOI: 10.3389/fphar.2021.615424; PMC: PMC8176440 HEBHMUi002-A 2021-00-00 2021-00-00 PubMed: 34093174 DOI: 10.3389/fphar.2021.615424Associated cell lines:
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Kamand M, Ilieva M, Forsberg SL, Thomassen M, Svenningsen ÅF, Meyer M, Michel TM
Generation of autism spectrum disorder patient-derived iPSC line SDUKIi004-A
Kamand M et al. Generation of autism spectrum disorder patient-derived iPSC line SDUKIi004-A. . 2020-12-00. Pubmed ID: 33068890; DOI: 10.1016/j.scr.2020.102038 SDUKIi002-ASDUKIi004-A 2020-12-00 2020-12-00 PubMed: 33068890 DOI: 10.1016/j.scr.2020.102038Associated cell lines:
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Paka Chloé A., Barrell William B., Monsoro-Burq Anne H., Liu Karen J.
Differentiation of human-induced pluripotent stem cells to the neural crest lineage
Paka Chloé A. et al. Differentiation of human-induced pluripotent stem cells to the neural crest lineage. . 2021-00-00. DOI: 10.1016/b978-0-12-823884-4.00014-6 KCi002-A 2021-00-00 2021-00-00 DOI: 10.1016/b978-0-12-823884-4.00014-6Associated cell lines:
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Hsu Yi-Chao, Tsai Chia-Ling
Differentiation of inner ear cell types from human-induced pluripotent stem cells for the therapeutic application in sensorineural hearing loss
Hsu Yi-Chao et al. Differentiation of inner ear cell types from human-induced pluripotent stem cells for the therapeutic application in sensorineural hearing loss. . 2021-00-00. DOI: 10.1016/b978-0-12-822230-0.00008-9 JUFMDOi004-AMMCi001-A 2021-00-00 2021-00-00 DOI: 10.1016/b978-0-12-822230-0.00008-9Associated cell lines:
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Peron C, Maresca A, Cavaliere A, Iannielli A, Broccoli V, Carelli V, Di Meo I, Tiranti V
Exploiting hiPSCs in Leber's Hereditary Optic Neuropathy (LHON): Present Achievements and Future Perspectives
Peron C et al. Exploiting hiPSCs in Leber's Hereditary Optic Neuropathy (LHON): Present Achievements and Future Perspectives. . 2021-00-00. Pubmed ID: 34168607; DOI: 10.3389/fneur.2021.648916; PMC: PMC8217617 FINCBi001-AFINCBi002-AFINCBi003-A 2021-00-00 2021-00-00 PubMed: 34168607 DOI: 10.3389/fneur.2021.648916Associated cell lines:
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Chu EP, Cho CH, Lee WJ, Lee IT, Cheng IF, Kuo TC, Chen RY, Sheu WH, Shen CN
Generation of three induced pluripotent stem cell lines from type 2 diabetic patients with ocular complications
Chu EP et al. Generation of three induced pluripotent stem cell lines from type 2 diabetic patients with ocular complications. . 2020-12-00. Pubmed ID: 33370876; DOI: 10.1016/j.scr.2020.102109 ASGRCi004-AASGRCi005-AASGRCi006-A 2020-12-00 2020-12-00 PubMed: 33370876 DOI: 10.1016/j.scr.2020.102109Associated cell lines:
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Li YP, Liu H, Jin ZB
Generation of three human iPSC lines from a retinitis pigmentosa family with SLC7A14 mutation
Li YP et al. Generation of three human iPSC lines from a retinitis pigmentosa family with SLC7A14 mutation. . 2020-12-00. Pubmed ID: 33207307; DOI: 10.1016/j.scr.2020.102075 WMUi003-AWMUi004-AWMUi005-A 2020-12-00 2020-12-00 PubMed: 33207307 DOI: 10.1016/j.scr.2020.102075 -
Vishwas S, Gulati M, Kapoor B, Gupta S, Singh SK, Awasthi A, Khan A, Goyal A, Bansal A, Baishnab S, Singh TG, Arora S, Porwal O, Kumar A, Kumar V
Expanding the Arsenal Against Huntington's Disease-Herbal Drugs and Their Nanoformulations
Vishwas S et al. Expanding the Arsenal Against Huntington's Disease-Herbal Drugs and Their Nanoformulations. . 2021-00-00. Pubmed ID: 33167841; DOI: 10.2174/1570159x18666201109090824; PMC: PMC8686322 CSSi004-ACSSi006-ALUMCi007-ALUMCi007-BLUMCi008-ALUMCi008-BICGi018-A 2021-00-00 2021-00-00 PubMed: 33167841 DOI: 10.2174/1570159x18666201109090824Associated cell lines:
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Bu Q, Zhang H, Liu Q, Dai Y, Wei Q, Xue A, Huang Y, Zhong K, Huang Y, Gao H, Cen X
Generation of an NANS homozygous knockout human induced pluripotent stem cell line by the insertion of GFP-P2A-Puro via CRISPR/Cas9 editing
Bu Q et al. Generation of an NANS homozygous knockout human induced pluripotent stem cell line by the insertion of GFP-P2A-Puro via CRISPR/Cas9 editing. . 2020-12-00. Pubmed ID: 33130469; DOI: 10.1016/j.scr.2020.102052 NCCSEDi001-ANCCSEDi001-A-1 2020-12-00 2020-12-00 PubMed: 33130469 DOI: 10.1016/j.scr.2020.102052Associated cell lines:
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Gosstola NC, Huang Z, Tong X, Nourbakhsh A, Chen ZY, Dykxhoorn DM, Zhong Liu X
Characterization of UMi028-A-1 stem cell line that contains a CRISPR/Cas9 induced hearing loss-associated variant (V60L (c.178G > T)) in the P2RX2 gene
Gosstola NC et al. Characterization of UMi028-A-1 stem cell line that contains a CRISPR/Cas9 induced hearing loss-associated variant (V60L (c.178G > T)) in the P2RX2 gene. . 2020-12-00. Pubmed ID: 33038743; DOI: 10.1016/j.scr.2020.102017 UMi028-AUMi028-A-1 2020-12-00 2020-12-00 PubMed: 33038743 DOI: 10.1016/j.scr.2020.102017Associated cell lines:
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Fulgencio-Covián A, Álvarez M, Pepers BA, López-Márquez A, Ugarte M, Pérez B, van Roon-Mom WMC, Desviat LR, Richard E
Generation of a gene-corrected human isogenic line (UAMi006-A) from propionic acidemia patient iPSC with an homozygous mutation in the PCCB gene using CRISPR/Cas9 technology
Fulgencio-Covián A et al. Generation of a gene-corrected human isogenic line (UAMi006-A) from propionic acidemia patient iPSC with an homozygous mutation in the PCCB gene using CRISPR/Cas9 technology. . 2020-12-00. Pubmed ID: 33128956; DOI: 10.1016/j.scr.2020.102055 UAMi004-AUAMi004-A-1 2020-12-00 2020-12-00 PubMed: 33128956 DOI: 10.1016/j.scr.2020.102055Associated cell lines:
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Guo X, Ji W, Niu C, Ding Y, Chen Z, Chen C, Tong H, Han Z, Chu M
Generation of an urine-derived induced pluripotent stem cell line from a 5-year old X-linked Alport syndrome (X-LAS) patient
Guo X et al. Generation of an urine-derived induced pluripotent stem cell line from a 5-year old X-linked Alport syndrome (X-LAS) patient. . 2020-12-00. Pubmed ID: 33202306; DOI: 10.1016/j.scr.2020.102085 WMUi015-A 2020-12-00 2020-12-00 PubMed: 33202306 DOI: 10.1016/j.scr.2020.102085Associated cell lines:
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Feng Y, Li X, Zhang L, Sun Y, He Y, Wen R, Hu Y, Wang X, Liu J, Long B
Generation of a RGS18 gene knockout cell line from a human embryonic stem cell line by CRISPR/Cas9
Feng Y et al. Generation of a RGS18 gene knockout cell line from a human embryonic stem cell line by CRISPR/Cas9. . 2020-12-00. Pubmed ID: 33157388; DOI: 10.1016/j.scr.2020.102072 WAe001-A-35 2020-12-00 2020-12-00 PubMed: 33157388 DOI: 10.1016/j.scr.2020.102072Associated cell lines:
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Nishihara H, Gastfriend BD, Soldati S, Perriot S, Mathias A, Sano Y, Shimizu F, Gosselet F, Kanda T, Palecek SP, Du Pasquier R, Shusta EV, Engelhardt B
Advancing human induced pluripotent stem cell-derived blood-brain barrier models for studying immune cell interactions
Nishihara H et al. Advancing human induced pluripotent stem cell-derived blood-brain barrier models for studying immune cell interactions. . 2020-12-00. Pubmed ID: 33124083; DOI: 10.1096/fj.202001507rr; PMC: PMC7686106 CHUVi001-ALNISi001-A 2020-12-00 2020-12-00 PubMed: 33124083 DOI: 10.1096/fj.202001507rrAssociated cell lines:
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Wang SH, Wang XP
Generation of an induced pluripotent stem cell (iPSC) line (THSJTUi001-A) from a Wilson's disease patient harboring a homozygous Arg778Leu mutation in ATP7B gene
Wang SH et al. Generation of an induced pluripotent stem cell (iPSC) line (THSJTUi001-A) from a Wilson's disease patient harboring a homozygous Arg778Leu mutation in ATP7B gene. . 2020-12-00. Pubmed ID: 33096383; DOI: 10.1016/j.scr.2020.102050 THSJTUi001-A 2020-12-00 2020-12-00 PubMed: 33096383 DOI: 10.1016/j.scr.2020.102050Associated cell lines:
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Malashicheva A, Perepelina K
Diversity of Nuclear Lamin A/C Action as a Key to Tissue-Specific Regulation of Cellular Identity in Health and Disease
Malashicheva A et al. Diversity of Nuclear Lamin A/C Action as a Key to Tissue-Specific Regulation of Cellular Identity in Health and Disease. . 2021-00-00. Pubmed ID: 34722546; DOI: 10.3389/fcell.2021.761469; PMC: PMC8548693 FAMRCi005-AFAMRCi005-BFAMRCi006-AFAMRCi006-BFAMRCi007-AFAMRCi007-B 2021-00-00 2021-00-00 PubMed: 34722546 DOI: 10.3389/fcell.2021.761469Associated cell lines:
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Del Dotto V, Carelli V
Dominant Optic Atrophy (DOA): Modeling the Kaleidoscopic Roles of OPA1 in Mitochondrial Homeostasis
Del Dotto V et al. Dominant Optic Atrophy (DOA): Modeling the Kaleidoscopic Roles of OPA1 in Mitochondrial Homeostasis. . 2021-00-00. Pubmed ID: 34177786; DOI: 10.3389/fneur.2021.681326; PMC: PMC8220150 IISHDOi003-A 2021-00-00 2021-00-00 PubMed: 34177786 DOI: 10.3389/fneur.2021.681326Associated cell lines:
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Huang M, Yang Z, Li Y, Lan H, Cyganek L, Yuecel G, Lang S, Bieback K, El-Battrawy I, Zhou X, Borggrefe M, Akin I
Dopamine D1/D5 Receptor Signaling Is Involved in Arrhythmogenesis in the Setting of Takotsubo Cardiomyopathy
Huang M et al. Dopamine D1/D5 Receptor Signaling Is Involved in Arrhythmogenesis in the Setting of Takotsubo Cardiomyopathy. . 2021-00-00. Pubmed ID: 35187102; DOI: 10.3389/fcvm.2021.777463; PMC: PMC8855058 UMGi124-AUMGi014-BUMGi130-A 2021-00-00 2021-00-00 PubMed: 35187102 DOI: 10.3389/fcvm.2021.777463 -
Chu EP, Lin CH, Cho CH, Cheng IF, Kuo TC, Chen RY, Liao CN, Cheng JC, Tsai JI, Wang PC, Chang SJ, Shen CN
Establishment of three human induced pluripotent stem cell lines from a type 1 diabetic family harboring sequence variants associated with autoimmunity
Chu EP et al. Establishment of three human induced pluripotent stem cell lines from a type 1 diabetic family harboring sequence variants associated with autoimmunity. . 2020-12-00. Pubmed ID: 33096384; DOI: 10.1016/j.scr.2020.102029 ASGRCi001-AASGRCi002-AASGRCi003-A 2020-12-00 2020-12-00 PubMed: 33096384 DOI: 10.1016/j.scr.2020.102029Associated cell lines:
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Zhu X, Zhang Y, Yang X, Hao C, Duan H
Gene Therapy for Neurodegenerative Disease: Clinical Potential and Directions
Zhu X et al. Gene Therapy for Neurodegenerative Disease: Clinical Potential and Directions. . 2021-00-00. Pubmed ID: 34194298; DOI: 10.3389/fnmol.2021.618171; PMC: PMC8236824 KEIUi001-A 2021-00-00 2021-00-00 PubMed: 34194298 DOI: 10.3389/fnmol.2021.618171Associated cell lines:
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Tang X, Chen Z, Tan X, Luo L, Liu X, Gong L, Li DW, Liu Y
Generation of a homozygous CRISPR/Cas9-mediated knockout H9 hESC subline for the CRB1 locus
Tang X et al. Generation of a homozygous CRISPR/Cas9-mediated knockout H9 hESC subline for the CRB1 locus. . 2020-12-00. Pubmed ID: 33128952; DOI: 10.1016/j.scr.2020.102057 ZOCi001-AWAe009-A-38 2020-12-00 2020-12-00 PubMed: 33128952 DOI: 10.1016/j.scr.2020.102057Associated cell lines:
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Sun L, Li J, Li E, Niu S, Qin Z, Zhi Q, Zhao J, Xiong H, Li Y, Jian L, Zhang L
CRISPR/Cas9 mediated establishment of a human CSRP3 compound heterozygous knockout hESC line to model cardiomyopathy and heart failure
Sun L et al. CRISPR/Cas9 mediated establishment of a human CSRP3 compound heterozygous knockout hESC line to model cardiomyopathy and heart failure. . 2020-12-00. Pubmed ID: 33176267; DOI: 10.1016/j.scr.2020.102077 WAe009-AWAe009-A-41 2020-12-00 2020-12-00 PubMed: 33176267 DOI: 10.1016/j.scr.2020.102077Associated cell lines:
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Souidi M, Amédro P, Meyer P, Desprat R, Lemaître JM, Rivier F, Lacampagne A, Meli AC
Generation of three Duchenne Muscular Dystrophy patient-specific induced pluripotent stem cell lines DMD_YoTaz_PhyMedEXp, DMD_RaPer_PhyMedEXp, DMD_OuMen_PhyMedEXp (INSRMi008-A, INSRMi009-A and INSRMi010-A)
Souidi M et al. Generation of three Duchenne Muscular Dystrophy patient-specific induced pluripotent stem cell lines DMD_YoTaz_PhyMedEXp, DMD_RaPer_PhyMedEXp, DMD_OuMen_PhyMedEXp (INSRMi008-A, INSRMi009-A and INSRMi010-A). . 2020-12-00. Pubmed ID: 33246213; DOI: 10.1016/j.scr.2020.102094 REGUi003-AINSRMi008-AINSRMi009-AINSRMi010-A 2020-12-00 2020-12-00 PubMed: 33246213 DOI: 10.1016/j.scr.2020.102094Associated cell lines:
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Lu L, Yu X, Cai Y, Sun M, Yang H
Application of CRISPR/Cas9 in Alzheimer's Disease
Lu L et al. Application of CRISPR/Cas9 in Alzheimer's Disease. . 2021-00-00. Pubmed ID: 34992519; DOI: 10.3389/fnins.2021.803894; PMC: PMC8724030 UMi028-AUMi028-A-2 2021-00-00 2021-00-00 PubMed: 34992519 DOI: 10.3389/fnins.2021.803894Associated cell lines:
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Ge N, Liu M, Zhu X, Krawczyk J, McInerney V, Shen S, O'Brien T, Prendiville T
Generation and characterization of two induced pluripotent stem cell lines (NUIGi038-A, NUIGi038-B) from dermal fibroblasts of a healthy individual
Ge N et al. Generation and characterization of two induced pluripotent stem cell lines (NUIGi038-A, NUIGi038-B) from dermal fibroblasts of a healthy individual. . 2020-12-00. Pubmed ID: 33002719; DOI: 10.1016/j.scr.2020.101996 NUIGi038-ANUIGi038-B 2020-12-00 2020-12-00 PubMed: 33002719 DOI: 10.1016/j.scr.2020.101996Associated cell lines:
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Kim J
Cellular reprogramming to model and study epigenetic alterations in cancer
Kim J. Cellular reprogramming to model and study epigenetic alterations in cancer. . 2020-12-00. Pubmed ID: 33202305; DOI: 10.1016/j.scr.2020.102062; PMC: PMC7768185 CHOPi001-A 2020-12-00 2020-12-00 PubMed: 33202305 DOI: 10.1016/j.scr.2020.102062Associated cell lines:
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Aires V, Coulon-Bainier C, Pavlovic A, Ebeling M, Schmucki R, Schweitzer C, Kueng E, Gutbier S, Harde E
CD22 Blockage Restores Age-Related Impairments of Microglia Surveillance Capacity
Aires V et al. CD22 Blockage Restores Age-Related Impairments of Microglia Surveillance Capacity. . 2021-00-00. Pubmed ID: 34140954; DOI: 10.3389/fimmu.2021.684430; PMC: PMC8204252 BIONi010-C 2021-00-00 2021-00-00 PubMed: 34140954 DOI: 10.3389/fimmu.2021.684430Associated cell lines:
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Shi L, Cui Y, Zhang G, Zhou X, Luan J, Han J
Establishment of a control induced pluripotent stem cell line SMBCi006-A from a healthy male donor
Shi L et al. Establishment of a control induced pluripotent stem cell line SMBCi006-A from a healthy male donor. . 2020-12-00. Pubmed ID: 33039803; DOI: 10.1016/j.scr.2020.102025 SMBCi006-A 2020-12-00 2020-12-00 PubMed: 33039803 DOI: 10.1016/j.scr.2020.102025Associated cell lines:
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Gridina MM, Orlova PA, Minina JM, Shitik EM, Lemskaya NA, Grishchenko IV, Dolskiy AA, Shorina AR, Maksimova YV, Yudkin DV, Serov OL
Establishment of an induced pluripotent stem cell line (ICGi026-A) from peripheral blood mononuclear cells of a patient with fragile X syndrome
Gridina MM et al. Establishment of an induced pluripotent stem cell line (ICGi026-A) from peripheral blood mononuclear cells of a patient with fragile X syndrome. . 2020-12-00. Pubmed ID: 33189043; DOI: 10.1016/j.scr.2020.102070 IMGTi003-AICGi026-A 2020-12-00 2020-12-00 PubMed: 33189043 DOI: 10.1016/j.scr.2020.102070Associated cell lines:
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Bing S, Nengqing L, Yi C, Dian L, Diyu C, Yingjun X, Lina H, Yinghong Y, Hongmei G, Xiaofang S
Generation of induced pluripotent stem cell GZHMCi002-A from peripheral blood mononuclear cells with APOB mutation
Bing S et al. Generation of induced pluripotent stem cell GZHMCi002-A from peripheral blood mononuclear cells with APOB mutation. . 2020-12-00. Pubmed ID: 33128957; DOI: 10.1016/j.scr.2020.102054 GZHMCi002-A 2020-12-00 2020-12-00 PubMed: 33128957 DOI: 10.1016/j.scr.2020.102054Associated cell lines:
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Ali E, Ferraro RM, Lanzi G, Masneri S, Piovani G, Mazzoldi EL, Serpieri V, Valente EM, Giordano L, Giliani SC
Generation of induced pluripotent stem cell (iPSC) lines from a Joubert syndrome patient with compound heterozygous mutations in C5orf42 gene
Ali E et al. Generation of induced pluripotent stem cell (iPSC) lines from a Joubert syndrome patient with compound heterozygous mutations in C5orf42 gene. . 2020-12-00. Pubmed ID: 33010677; DOI: 10.1016/j.scr.2020.102007 UNIBSi011-AUNIBSi011-BUNIBSi011-C 2020-12-00 2020-12-00 PubMed: 33010677 DOI: 10.1016/j.scr.2020.102007Associated cell lines:
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Gridina MM, Nikitina TV, Orlova PA, Minina JM, Kashevarova AA, Yakovleva YS, Lopatkina ME, Vasilyev SA, Fedotov DA, Mikhailik LI, Nazarenko LP, Lebedev IN, Serov OL
Establishment of an induced pluripotent stem cell line (ICGi025-A) from fibroblasts of a patient with 46,XY,r(8)/45,XY,-8 mosaicism
Gridina MM et al. Establishment of an induced pluripotent stem cell line (ICGi025-A) from fibroblasts of a patient with 46,XY,r(8)/45,XY,-8 mosaicism. . 2020-12-00. Pubmed ID: 33070101; DOI: 10.1016/j.scr.2020.102024 ICGi025-A 2020-12-00 2020-12-00 PubMed: 33070101 DOI: 10.1016/j.scr.2020.102024Associated cell lines:
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Alowaysi M, Fiacco E, Astro V, Adamo A
Generation of two iPSC lines (KAUSTi001-A, KAUSTi002-A) from a rare high-grade Klinefelter Syndrome patient (49-XXXXY) carrying a balanced translocation t(4,11) (q35,q23)
Alowaysi M et al. Generation of two iPSC lines (KAUSTi001-A, KAUSTi002-A) from a rare high-grade Klinefelter Syndrome patient (49-XXXXY) carrying a balanced translocation t(4,11) (q35,q23). . 2020-12-00. Pubmed ID: 33254093; DOI: 10.1016/j.scr.2020.102098 KAUSTi001-AKAUSTi003-AKAUSTi004-AKAUSTi004-BKAUSTi005-AKAUSTi005-BKAUSTi005-CKAUSTi001-BKAUSTi006-AKAUSTi006-B 2020-12-00 2020-12-00 PubMed: 33254093 DOI: 10.1016/j.scr.2020.102098Associated cell lines:
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Long P, Wang Z, Yang H, Liu Z, Wu B, Zhong G, Chen J, Sun C, Wang F, Zhou Y, Sun F, Li Q, Ma Y
Generation of nine iPSC lines (HNMUi002-A, HNMUi003-A, HNMUi004-A, HNMUi005-A, HNMUi006-A, HNMUi007-A, HNMUi008-A, HNMUi009-A, HNMUi010-A) from three Chinese families with thalassemia
Long P et al. Generation of nine iPSC lines (HNMUi002-A, HNMUi003-A, HNMUi004-A, HNMUi005-A, HNMUi006-A, HNMUi007-A, HNMUi008-A, HNMUi009-A, HNMUi010-A) from three Chinese families with thalassemia. . 2020-12-00. Pubmed ID: 33039806; DOI: 10.1016/j.scr.2020.102014 HNMUi002-AHNMUi003-AHNMUi004-AHNMUi005-AHNMUi006-AHNMUi007-AHNMUi008-AHNMUi009-AHNMUi010-A 2020-12-00 2020-12-00 PubMed: 33039806 DOI: 10.1016/j.scr.2020.102014Associated cell lines:
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Hagiwara Daisuke, Suga Hidetaka, Arima Hiroshi
Generation of Hypothalamus and Adenohypophysis from Human Pluripotent Stem Cells
Hagiwara Daisuke et al. Generation of Hypothalamus and Adenohypophysis from Human Pluripotent Stem Cells. . 2021-00-00. DOI: 10.1007/978-3-030-86630-3_3 FHUi003-AFHUi003-BFHUi004-AFHUi004-B 2021-00-00 2021-00-00 DOI: 10.1007/978-3-030-86630-3_3 -
Ge N, Liu M, Krawczyk J, McInerney V, Ward D, Shen S, O'Brien T, Prendiville T
Generation and characterization of an induced pluripotent stem cell (iPSC) line (NUIGi003-A) from a long QT syndrome type 2 (LQT2) patient harbouring the KCNH2 c.2464G>A pathogenic variant
Ge N et al. Generation and characterization of an induced pluripotent stem cell (iPSC) line (NUIGi003-A) from a long QT syndrome type 2 (LQT2) patient harbouring the KCNH2 c.2464G>A pathogenic variant. . 2020-12-00. Pubmed ID: 33002718; DOI: 10.1016/j.scr.2020.101997 NUIGi003-A 2020-12-00 2020-12-00 PubMed: 33002718 DOI: 10.1016/j.scr.2020.101997Associated cell lines:
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Güner F, Pozner T, Krach F, Prots I, Loskarn S, Schlötzer-Schrehardt U, Winkler J, Winner B, Regensburger M
Axon-Specific Mitochondrial Pathology in SPG11 Alpha Motor Neurons
Güner F et al. Axon-Specific Mitochondrial Pathology in SPG11 Alpha Motor Neurons. . 2021-00-00. Pubmed ID: 34326717; DOI: 10.3389/fnins.2021.680572; PMC: PMC8314181 UKERi006-B 2021-00-00 2021-00-00 PubMed: 34326717 DOI: 10.3389/fnins.2021.680572Associated cell lines:
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Lee SJ, Kim JH, Kang KW, Lee BH, Kim BS
Generation of normal induced pluripotent stem cell line KUMCi002-A from bone marrow CD34+ cells of patient with multiple myeloma disease having 13q deletion and IGH translocation
Lee SJ et al. Generation of normal induced pluripotent stem cell line KUMCi002-A from bone marrow CD34+ cells of patient with multiple myeloma disease having 13q deletion and IGH translocation. . 2020-12-00. Pubmed ID: 33142253; DOI: 10.1016/j.scr.2020.102030 KUMCi001-AKUMCi002-A 2020-12-00 2020-12-00 PubMed: 33142253 DOI: 10.1016/j.scr.2020.102030Associated cell lines:
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Hsia GSP, Esposito J, da Rocha LA, Ramos SLG, Okamoto OK
Clinical Application of Human Induced Pluripotent Stem Cell-Derived Organoids as an Alternative to Organ Transplantation
Hsia GSP et al. Clinical Application of Human Induced Pluripotent Stem Cell-Derived Organoids as an Alternative to Organ Transplantation. . 2021-00-00. Pubmed ID: 33679987; DOI: 10.1155/2021/6632160; PMC: PMC7929656 WAe009-A 2021-00-00 2021-00-00 PubMed: 33679987 DOI: 10.1155/2021/6632160Associated cell lines:
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Barbeau S, Desprat R, Eymard B, Martinat C, Lemaitre JM, Legay C
Generation of a human induced pluripotent stem cell line (iPSC) from peripheral blood mononuclear cells of a patient with a myasthenic syndrome due to mutation in COLQ
Barbeau S et al. Generation of a human induced pluripotent stem cell line (iPSC) from peripheral blood mononuclear cells of a patient with a myasthenic syndrome due to mutation in COLQ. . 2020-12-00. Pubmed ID: 33370874; DOI: 10.1016/j.scr.2020.102106 REGUi009-A 2020-12-00 2020-12-00 PubMed: 33370874 DOI: 10.1016/j.scr.2020.102106Associated cell lines:
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Vajhøj C, Schmid B, Alik A, Melki R, Fog K, Holst B, Stummann TC
Establishment of a human induced pluripotent stem cell neuronal model for identification of modulators of A53T α-synuclein levels and aggregation
Vajhøj C et al. Establishment of a human induced pluripotent stem cell neuronal model for identification of modulators of A53T α-synuclein levels and aggregation. . 2021-00-00. Pubmed ID: 34932569; DOI: 10.1371/journal.pone.0261536; PMC: PMC8691628 BIONi010-CBIONi010-C-24 2021-00-00 2021-00-00 PubMed: 34932569 DOI: 10.1371/journal.pone.0261536Associated cell lines:
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Zhang C, Yu Y, Li F, Lan X, Wang L
Generating an MEIS1 homozygous knockout human embryonic stem cell line using the CRISPR/Cas9 system
Zhang C et al. Generating an MEIS1 homozygous knockout human embryonic stem cell line using the CRISPR/Cas9 system. . 2020-12-00. Pubmed ID: 33157390; DOI: 10.1016/j.scr.2020.102069 WAe001-AWAe001-A-49 2020-12-00 2020-12-00 PubMed: 33157390 DOI: 10.1016/j.scr.2020.102069Associated cell lines:
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Ding Y, Wang L, Ji W, Chen Z, Wang D, Chen C, Tong H, Han Z, Niu C, Chu M, Huang J, Guo X
Generation of a human induced pluripotent stem cell line with Cas9 driven by Tet-on operator via AAVS1 safe harbor gene-editing
Ding Y et al. Generation of a human induced pluripotent stem cell line with Cas9 driven by Tet-on operator via AAVS1 safe harbor gene-editing. . 2020-12-00. Pubmed ID: 33207306; DOI: 10.1016/j.scr.2020.102064 WMUi013-A 2020-12-00 2020-12-00 PubMed: 33207306 DOI: 10.1016/j.scr.2020.102064Associated cell lines:
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Kim DH, Park CY, Cho SR, Kim DW
Generation of a human induced pluripotent stem cell line, YCMi002-A, from a Factor VII deficiency patient carrying F7 mutations
Kim DH et al. Generation of a human induced pluripotent stem cell line, YCMi002-A, from a Factor VII deficiency patient carrying F7 mutations. . 2020-12-00. Pubmed ID: 33038747; DOI: 10.1016/j.scr.2020.102026 YCMi002-A 2020-12-00 2020-12-00 PubMed: 33038747 DOI: 10.1016/j.scr.2020.102026Associated cell lines:
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Ding Y, de la Cruz BM, McInerney V, Lu Y, Yang G, Qian X, Li W, Krawczyk J, Howard L, O'Brien T, Gallagher L, Shen S
Derivation of iPSC lines from three young healthy donors of Caucasian origin (NUIGi035-A; NUIGi036-A; NUIGi037-A)
Ding Y et al. Derivation of iPSC lines from three young healthy donors of Caucasian origin (NUIGi035-A; NUIGi036-A; NUIGi037-A). . 2020-12-00. Pubmed ID: 33370872; DOI: 10.1016/j.scr.2020.102101 NUIGi035-ANUIGi036-ANUIGi037-A 2020-12-00 2020-12-00 PubMed: 33370872 DOI: 10.1016/j.scr.2020.102101Associated cell lines:
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Ahmed M, Owens MJS, Toledo EM, Arenas E, Bradley M, Ffrench-Constant C
Combinatorial ECM Arrays Identify Cooperative Roles for Matricellular Proteins in Enhancing the Generation of TH+ Neurons From Human Pluripotent Cells
Ahmed M et al. Combinatorial ECM Arrays Identify Cooperative Roles for Matricellular Proteins in Enhancing the Generation of TH+ Neurons From Human Pluripotent Cells. . 2021-00-00. Pubmed ID: 34926447; DOI: 10.3389/fcell.2021.755406; PMC: PMC8672163 RCe021-A 2021-00-00 2021-00-00 PubMed: 34926447 DOI: 10.3389/fcell.2021.755406Associated cell lines:
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Katagami Y, Kondo T, Suga M, Yada Y, Imamura K, Shibukawa R, Sagara Y, Okanishi Y, Tsukita K, Hirayama K, Era T, Inoue H
Generation of a human induced pluripotent stem cell line, BRCi009-A, derived from a patient with glycogen storage disease type 1a
Katagami Y et al. Generation of a human induced pluripotent stem cell line, BRCi009-A, derived from a patient with glycogen storage disease type 1a. . 2020-12-00. Pubmed ID: 33291009; DOI: 10.1016/j.scr.2020.102095 BRCi009-A 2020-12-00 2020-12-00 PubMed: 33291009 DOI: 10.1016/j.scr.2020.102095Associated cell lines:
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Rizki-Safitri A, Traitteur T, Morizane R
Bioengineered Kidney Models: Methods and Functional Assessments
Rizki-Safitri A et al. Bioengineered Kidney Models: Methods and Functional Assessments. . 2021-00-00. Pubmed ID: 35330622; DOI: 10.1093/function/zqab026; PMC: PMC8788738 WISCi004-ABCRTi004-ABCRTi005-A 2021-00-00 2021-00-00 PubMed: 35330622 DOI: 10.1093/function/zqab026Associated cell lines:
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Kuebler B, Aran B, Flores R, Pérez-Jurado LA, Veiga A, Cuscó I, Corominas R
Derivation of induced pluripotent stem cells (iPSCs) by retroviral transduction of skin fibroblasts from four patients suffering 7q11.23 microduplication syndrome
Kuebler B et al. Derivation of induced pluripotent stem cells (iPSCs) by retroviral transduction of skin fibroblasts from four patients suffering 7q11.23 microduplication syndrome. . 2020-12-00. Pubmed ID: 33254092; DOI: 10.1016/j.scr.2020.102092 ESi057-BESi058-BESi070-AESi071-A 2020-12-00 2020-12-00 PubMed: 33254092 DOI: 10.1016/j.scr.2020.102092 -
Chakritbudsabong W, Sariya L, Jantahiran P, Chaisilp N, Chaiwattanarungruengpaisan S, Rungsiwiwut R, Ferreira JN, Rungarunlert S
Generation of Porcine Induced Neural Stem Cells Using the Sendai Virus
Chakritbudsabong W et al. Generation of Porcine Induced Neural Stem Cells Using the Sendai Virus. . 2021-00-00. Pubmed ID: 35097051; DOI: 10.3389/fvets.2021.806785; PMC: PMC8790232 MDCUi001-AMDCUi001-B 2021-00-00 2021-00-00 PubMed: 35097051 DOI: 10.3389/fvets.2021.806785Associated cell lines:
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Mukherjee S, Gagne AL, Maguire JA, Jobaliya CD, Mills JA, Gadue P, French DL
Generation of human control iPSC line CHOPi004-A from juvenile foreskin fibroblast cells
Mukherjee S et al. Generation of human control iPSC line CHOPi004-A from juvenile foreskin fibroblast cells. . 2020-12-00. Pubmed ID: 33202304; DOI: 10.1016/j.scr.2020.102084 CHOPi004-A 2020-12-00 2020-12-00 PubMed: 33202304 DOI: 10.1016/j.scr.2020.102084Associated cell lines:
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Ababneh NA, Al-Kurdi B, Barham R, Ali D, Sharar N, Abuarqoub D, Jafar H, Salah B, Awidi A
Derivation of three human induced pluripotent stem cell lines (JUCTCi014-A, JUCTCi015-A, JUCTCi016-A) from mesenchymal stem cells (MSCs) derived from bone marrow, adipose tissue and Wharton's jelly samples
Ababneh NA et al. Derivation of three human induced pluripotent stem cell lines (JUCTCi014-A, JUCTCi015-A, JUCTCi016-A) from mesenchymal stem cells (MSCs) derived from bone marrow, adipose tissue and Wharton's jelly samples. . 2020-12-00. Pubmed ID: 33010679; DOI: 10.1016/j.scr.2020.102000 JUCTCi014-AJUCTCi015-AJUCTCi016-A 2020-12-00 2020-12-00 PubMed: 33010679 DOI: 10.1016/j.scr.2020.102000Associated cell lines:
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Xu X, Pradhan M, Xu M, Cheng YS, Beers J, Linask KL, Lin Y, Zheng W, Zou J
Four induced pluripotent stem cell lines (TRNDi021-C, TRNDi023-D, TRNDi024-D and TRNDi025-A) generated from fibroblasts of four healthy individuals
Xu X et al. Four induced pluripotent stem cell lines (TRNDi021-C, TRNDi023-D, TRNDi024-D and TRNDi025-A) generated from fibroblasts of four healthy individuals. . 2020-12-00. Pubmed ID: 33038742; DOI: 10.1016/j.scr.2020.102011; PMC: PMC7810501 TRNDi021-CTRNDi023-DTRNDi024-DTRNDi025-A 2020-12-00 2020-12-00 PubMed: 33038742 DOI: 10.1016/j.scr.2020.102011Associated cell lines:
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Wang G, Wu H, Gao E, Zhang L, Chen L, Zhu Y, Zhang J, Liu Z
Generation of induced pluripotent stem cell line (NCKDi001-A) from a 19-year-old patient with a novel COL4A5 gene mutation in Alport syndrome
Wang G et al. Generation of induced pluripotent stem cell line (NCKDi001-A) from a 19-year-old patient with a novel COL4A5 gene mutation in Alport syndrome. . 2020-12-00. Pubmed ID: 33128955; DOI: 10.1016/j.scr.2020.102023 NCKDi001-A 2020-12-00 2020-12-00 PubMed: 33128955 DOI: 10.1016/j.scr.2020.102023Associated cell lines:
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Zhu YJ, Zhang SJ, Wu XH, Lian TY, He YZ, Zhang ZJ, Lu D, Sun K, Wang HF, Jing ZC
Generation of an induced pluripotent stem cell line (PUMCHi006-A) derived from a patient with pulmonary arterial hypertension carrying heterozygous c.1339 G > A mutation in PTGIS gene
Zhu YJ et al. Generation of an induced pluripotent stem cell line (PUMCHi006-A) derived from a patient with pulmonary arterial hypertension carrying heterozygous c.1339 G > A mutation in PTGIS gene. . 2020-12-00. Pubmed ID: 33221675; DOI: 10.1016/j.scr.2020.102088 PUMCHi003-APUMCHi006-A 2020-12-00 2020-12-00 PubMed: 33221675 DOI: 10.1016/j.scr.2020.102088Associated cell lines:
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Xiong J, Liu Z, Chen S, Kessi M, Chen B, Duan H, Deng X, Yang L, Peng J, Yin F
Correlation Analyses of Clinical Manifestations and Variant Effects in KCNB1-Related Neurodevelopmental Disorder
Xiong J et al. Correlation Analyses of Clinical Manifestations and Variant Effects in KCNB1-Related Neurodevelopmental Disorder. . 2021-00-00. Pubmed ID: 35071126; DOI: 10.3389/fped.2021.755344; PMC: PMC8767024 ZJSHi001-A 2021-00-00 2021-00-00 PubMed: 35071126 DOI: 10.3389/fped.2021.755344Associated cell lines:
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Molina SG, Beltran AA, Beltran AS
Generation of an integration-free induced pluripotent stem cell line (UNC001-A) from blood of a healthy individual
Molina SG et al. Generation of an integration-free induced pluripotent stem cell line (UNC001-A) from blood of a healthy individual. . 2020-12-00. Pubmed ID: 33038744; DOI: 10.1016/j.scr.2020.102015 UNCi001-A 2020-12-00 2020-12-00 PubMed: 33038744 DOI: 10.1016/j.scr.2020.102015Associated cell lines:
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Li J, Li Y, Zhan XY, Ran X, Tse HF, Dang S, Nie Y, Huang K
Generation of GADD45A gene knockout human embryonic stem cell line using CRISPR/Cas9
Li J et al. Generation of GADD45A gene knockout human embryonic stem cell line using CRISPR/Cas9. . 2020-12-00. Pubmed ID: 33232900; DOI: 10.1016/j.scr.2020.102090 WAe001-A-59 2020-12-00 2020-12-00 PubMed: 33232900 DOI: 10.1016/j.scr.2020.102090Associated cell lines:
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Alowaysi M, Fiacco E, Astro V, Adamo A
Establishment of an iPSC cohort from three unrelated 47-XXY Klinefelter Syndrome patients (KAUSTi007-A, KAUSTi007-B, KAUSTi009-A, KAUSTi009-B, KAUSTi010-A, KAUSTi010-B)
Alowaysi M et al. Establishment of an iPSC cohort from three unrelated 47-XXY Klinefelter Syndrome patients (KAUSTi007-A, KAUSTi007-B, KAUSTi009-A, KAUSTi009-B, KAUSTi010-A, KAUSTi010-B). . 2020-12-00. Pubmed ID: 33068889; DOI: 10.1016/j.scr.2020.102042 KAUSTi003-AKAUSTi004-AKAUSTi004-BKAUSTi005-AKAUSTi005-BKAUSTi005-CKAUSTi007-AKAUSTi007-BKAUSTi009-AKAUSTi009-BKAUSTi010-AKAUSTi010-B 2020-12-00 2020-12-00 PubMed: 33068889 DOI: 10.1016/j.scr.2020.102042Associated cell lines:
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He S, Jin Y, Tian Z, Hua T, Xing H, Zhuang S, He X, Li H, Wang L, Zhang S
Establishment of an induced pluripotent stem cell line PUMCHi004-A from a hereditary transthyretin amyloid cardiomyopathy patient with transthyretin (TTR) p.Asp38Asn mutation
He S et al. Establishment of an induced pluripotent stem cell line PUMCHi004-A from a hereditary transthyretin amyloid cardiomyopathy patient with transthyretin (TTR) p.Asp38Asn mutation. . 2020-12-00. Pubmed ID: 33038745; DOI: 10.1016/j.scr.2020.102022 PUMCHi004-A 2020-12-00 2020-12-00 PubMed: 33038745 DOI: 10.1016/j.scr.2020.102022Associated cell lines:
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Ohta E, Sone T, Ukai H, Hisamatsu T, Kitagawa T, Ishikawa M, Nagai M, Ueda HR, Obata F, Okano H
Generation of gene-corrected iPSCs line (KEIUi001-A) from a PARK8 patient iPSCs with familial Parkinson's disease carrying the I2020T mutation in LRRK2
Ohta E et al. Generation of gene-corrected iPSCs line (KEIUi001-A) from a PARK8 patient iPSCs with familial Parkinson's disease carrying the I2020T mutation in LRRK2. . 2020-12-00. Pubmed ID: 33181472; DOI: 10.1016/j.scr.2020.102073 KEIUi001-A 2020-12-00 2020-12-00 PubMed: 33181472 DOI: 10.1016/j.scr.2020.102073Associated cell lines:
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Gong P, Jiao X, Zhang Y, Yang Z
Generation of a human iPSC line from an epileptic encephalopathy patient with electrical status epilepticus during sleep carrying KCNA2 (p.P405L) mutation
Gong P et al. Generation of a human iPSC line from an epileptic encephalopathy patient with electrical status epilepticus during sleep carrying KCNA2 (p.P405L) mutation. . 2020-12-00. Pubmed ID: 33232902; DOI: 10.1016/j.scr.2020.102080 PUFHi001-A 2020-12-00 2020-12-00 PubMed: 33232902 DOI: 10.1016/j.scr.2020.102080Associated cell lines:
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Sun Y, Liu G, Huang Y
Applications of piggyBac Transposons for Genome Manipulation in Stem Cells
Sun Y et al. Applications of piggyBac Transposons for Genome Manipulation in Stem Cells. . 2021-00-00. Pubmed ID: 34567130; DOI: 10.1155/2021/3829286; PMC: PMC8460389 WAe001-AWAe001-A-58 2021-00-00 2021-00-00 PubMed: 34567130 DOI: 10.1155/2021/3829286Associated cell lines:
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Vaz IM, Borgonovo T, Kasai-Brunswick TH, Santos DSD, Mesquita FCP, Vasques JF, Gubert F, Rebelatto CLK, Senegaglia AC, Brofman PRS
Chromosomal aberrations after induced pluripotent stem cells reprogramming
Vaz IM et al. Chromosomal aberrations after induced pluripotent stem cells reprogramming. . 2021-00-00. Pubmed ID: 34496008; DOI: 10.1590/1678-4685-gmb-2020-0147; PMC: PMC8425414 IMGTi001-AIMGTi001-BUFRJi007-A 2021-00-00 2021-00-00 PubMed: 34496008 DOI: 10.1590/1678-4685-gmb-2020-0147Associated cell lines:
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Zhu S, Law AHY, Deng R, Poon ENY, Lo CW, Kwong AKY, Liang R, Chan KYK, Wong WL, Tan-Un KC, Pijnappel WWMP, Chan GCF, Chan SHS
Generation of genomic-integration-free human induced pluripotent stem cells and the derived cardiomyocytes of X-linked dilated cardiomyopathy from DMD gene mutation
Zhu S et al. Generation of genomic-integration-free human induced pluripotent stem cells and the derived cardiomyocytes of X-linked dilated cardiomyopathy from DMD gene mutation. . 2020-12-00. Pubmed ID: 33099108; DOI: 10.1016/j.scr.2020.102040 HKUi002-A 2020-12-00 2020-12-00 PubMed: 33099108 DOI: 10.1016/j.scr.2020.102040Associated cell lines:
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Yan R, Liu P, Li F, Chu M, Lei J, Wang F, Luo L, Xu X
Generation of a human induced pluripotent stem cell line (SBWCHi001-A) from a patient with NEDSDV carrying a pathogenic mutation in CTNNB1 gene
Yan R et al. Generation of a human induced pluripotent stem cell line (SBWCHi001-A) from a patient with NEDSDV carrying a pathogenic mutation in CTNNB1 gene. . 2020-12-00. Pubmed ID: 33264726; DOI: 10.1016/j.scr.2020.102091 SBWCHi001-A 2020-12-00 2020-12-00 PubMed: 33264726 DOI: 10.1016/j.scr.2020.102091Associated cell lines:
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Petters J, Völkner C, Krohn S, Murua Escobar H, Bullerdiek J, Reuner U, Frech MJ, Hermann A, Lukas J
Generation of two induced pluripotent stem cell lines from a female adult homozygous for the Wilson disease associated ATP7B variant p.H1069Q (AKOSi008-A) and a healthy control (AKOSi009-A)
Petters J et al. Generation of two induced pluripotent stem cell lines from a female adult homozygous for the Wilson disease associated ATP7B variant p.H1069Q (AKOSi008-A) and a healthy control (AKOSi009-A). . 2020-12-00. Pubmed ID: 33197697; DOI: 10.1016/j.scr.2020.102079 AKOSi008-AAKOSi009-A 2020-12-00 2020-12-00 PubMed: 33197697 DOI: 10.1016/j.scr.2020.102079Associated cell lines:
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Wu S, Wei H, Chu M, Weng Z
Generation of a human iPSC line CIBi008-A from amniotic fluid-derived cells of a fetus with β-thalassemia carrying variants of -28A > G and IVS-II-654C > T in HBB
Wu S et al. Generation of a human iPSC line CIBi008-A from amniotic fluid-derived cells of a fetus with β-thalassemia carrying variants of -28A > G and IVS-II-654C > T in HBB. . 2020-12-00. Pubmed ID: 33157391; DOI: 10.1016/j.scr.2020.102074 CIBi008-A 2020-12-00 2020-12-00 PubMed: 33157391 DOI: 10.1016/j.scr.2020.102074Associated cell lines:
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Fiacco E, Alowaysi M, Astro V, Adamo A
Derivation of two naturally isogenic iPSC lines (KAUSTi006-A and KAUSTi006-B) from a mosaic Klinefelter Syndrome patient (47-XXY/46-XY)
Fiacco E et al. Derivation of two naturally isogenic iPSC lines (KAUSTi006-A and KAUSTi006-B) from a mosaic Klinefelter Syndrome patient (47-XXY/46-XY). . 2020-12-00. Pubmed ID: 33096382; DOI: 10.1016/j.scr.2020.102049 KAUSTi003-AKAUSTi004-AKAUSTi004-BKAUSTi005-AKAUSTi005-BKAUSTi005-CKAUSTi006-AKAUSTi006-B 2020-12-00 2020-12-00 PubMed: 33096382 DOI: 10.1016/j.scr.2020.102049Associated cell lines:
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Gilmozzi V, Gentile G, Riekschnitz DA, Von Troyer M, Lavdas AA, Kerschbamer E, Weichenberger CX, Rosato-Siri MD, Casarosa S, Conti L, Pramstaller PP, Hicks AA, Pichler I, Zanon A
Generation of hiPSC-Derived Functional Dopaminergic Neurons in Alginate-Based 3D Culture
Gilmozzi V et al. Generation of hiPSC-Derived Functional Dopaminergic Neurons in Alginate-Based 3D Culture. . 2021-00-00. Pubmed ID: 34409038; DOI: 10.3389/fcell.2021.708389; PMC: PMC8365765 STBCi033-B 2021-00-00 2021-00-00 PubMed: 34409038 DOI: 10.3389/fcell.2021.708389Associated cell lines:
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Besusso D, Cossu A, Mohamed A, Cernigoj M, Codega P, Galimberti M, Campus I, Conforti P, Cattaneo E
A CRISPR-strategy for the generation of a detectable fluorescent hESC reporter line (WAe009-A-37) for the subpallial determinant GSX2
Besusso D et al. A CRISPR-strategy for the generation of a detectable fluorescent hESC reporter line (WAe009-A-37) for the subpallial determinant GSX2. . 2020-12-00. Pubmed ID: 33039807; DOI: 10.1016/j.scr.2020.102016 WAe009-AWAe009-A-37 2020-12-00 2020-12-00 PubMed: 33039807 DOI: 10.1016/j.scr.2020.102016Associated cell lines:
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Nagel M, Müßig S, Höflinger P, Schöls L, Hauser S, Schüle R
Generation of the CRISPR/Cas9-mediated KIF1C knock-out human iPSC line HIHRSi003-A-1
Nagel M et al. Generation of the CRISPR/Cas9-mediated KIF1C knock-out human iPSC line HIHRSi003-A-1. . 2020-12-00. Pubmed ID: 33161238; DOI: 10.1016/j.scr.2020.102059 HIHRSi003-AHIHRSi003-A-1 2020-12-00 2020-12-00 PubMed: 33161238 DOI: 10.1016/j.scr.2020.102059Associated cell lines:
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Pansri P, Phanthong P, Suthprasertporn N, Kitiyanant Y, Tubsuwan A, Dinnyes A, Kobolak J, Kitiyanant N
Brain-derived neurotrophic factor increases cell number of neural progenitor cells derived from human induced pluripotent stem cells
Pansri P et al. Brain-derived neurotrophic factor increases cell number of neural progenitor cells derived from human induced pluripotent stem cells. . 2021-00-00. Pubmed ID: 34026357; DOI: 10.7717/peerj.11388; PMC: PMC8123227 BIOTi001-A 2021-00-00 2021-00-00 PubMed: 34026357 DOI: 10.7717/peerj.11388Associated cell lines:
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Zhao H, Li S, Lin Z, He L, Deng W, Han X, Tang F, Cheng N, Zhou P, Huang R, Deng S, Huang J, Li Z
A heterozygous SCN1A (c.A5768G/+) mutant human induced pluripotent stem cell line (USTCi002-A) generated using TALEN-mediated precise gene editing
Zhao H et al. A heterozygous SCN1A (c.A5768G/+) mutant human induced pluripotent stem cell line (USTCi002-A) generated using TALEN-mediated precise gene editing. . 2020-12-00. Pubmed ID: 33189042; DOI: 10.1016/j.scr.2020.102058 USTCi001-AUSTCi001-A-1USTCi002-A 2020-12-00 2020-12-00 PubMed: 33189042 DOI: 10.1016/j.scr.2020.102058Associated cell lines:
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Potjewyd FM, Axtman AD
Exploration of Aberrant E3 Ligases Implicated in Alzheimer's Disease and Development of Chemical Tools to Modulate Their Function
Potjewyd FM et al. Exploration of Aberrant E3 Ligases Implicated in Alzheimer's Disease and Development of Chemical Tools to Modulate Their Function. . 2021-00-00. Pubmed ID: 34867205; DOI: 10.3389/fncel.2021.768655; PMC: PMC8637409 UMi028-AUMi028-A-2 2021-00-00 2021-00-00 PubMed: 34867205 DOI: 10.3389/fncel.2021.768655Associated cell lines:
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Ahmed Engi, Fieldes Mathieu, Bourguignon Chloé, Mianné Joffrey, Petit Aurélie, Vernisse Charlotte, Jory Myriam, Cazevieille Chantal, Boukhaddaoui Hassan, Garnett James P., Massiera Gladys, Vachier Isabelle, Assou Said, Bourdin Arnaud, De Vos John
Differentiation of human induced pluripotent stem cells into functional airway epithelium
Ahmed Engi et al. Differentiation of human induced pluripotent stem cells into functional airway epithelium. . 2020-11-29. DOI: 10.1101/2020.11.29.400358 UHOMi001-AUHOMi002-AUHOMi003-AUHOMi004-AUHOMi005-A 2020-11-29 2020-11-29 DOI: 10.1101/2020.11.29.400358Associated cell lines:
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Kiang AS, Kenna PF, Humphries MM, Ozaki E, Koenekoop RK, Campbell M, Farrar GJ, Humphries P
Properties and Therapeutic Implications of an Enigmatic D477G RPE65 Variant Associated with Autosomal Dominant Retinitis Pigmentosa
Kiang AS et al. Properties and Therapeutic Implications of an Enigmatic D477G RPE65 Variant Associated with Autosomal Dominant Retinitis Pigmentosa. . 2020-11-27. Pubmed ID: 33261050; DOI: 10.3390/genes11121420; PMC: PMC7760593 NUIGi027-ANUIGi028-ANUIGi029-A 2020-11-27 2020-11-27 PubMed: 33261050 DOI: 10.3390/genes11121420Associated cell lines:
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Pallottini V, Pfrieger FW
Understanding and Treating Niemann-Pick Type C Disease: Models Matter
Pallottini V et al. Understanding and Treating Niemann-Pick Type C Disease: Models Matter. . 2020-11-26. Pubmed ID: 33256121; DOI: 10.3390/ijms21238979; PMC: PMC7730076 AKOSi001-A 2020-11-26 2020-11-26 PubMed: 33256121 DOI: 10.3390/ijms21238979Associated cell lines:
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Szepes M, Melchert A, Dahlmann J, Hegermann J, Werlein C, Jonigk D, Haverich A, Martin U, Olmer R, Gruh I
Dual Function of iPSC-Derived Pericyte-Like Cells in Vascularization and Fibrosis-Related Cardiac Tissue Remodeling In Vitro
Szepes M et al. Dual Function of iPSC-Derived Pericyte-Like Cells in Vascularization and Fibrosis-Related Cardiac Tissue Remodeling In Vitro. . 2020-11-25. Pubmed ID: 33255686; DOI: 10.3390/ijms21238947; PMC: PMC7728071 MHHi006-AMHHi009-AMHHi009-A-4 2020-11-25 2020-11-25 PubMed: 33255686 DOI: 10.3390/ijms21238947Associated cell lines:
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Bernard EM, Fearns A, Bussi C, Santucci P, Peddie CJ, Lai RJ, Collinson LM, Gutierrez MG
M. tuberculosis infection of human iPSC-derived macrophages reveals complex membrane dynamics during xenophagy evasion
Bernard EM et al. M. tuberculosis infection of human iPSC-derived macrophages reveals complex membrane dynamics during xenophagy evasion. . 2020-11-25. Pubmed ID: 32938685; DOI: 10.1242/jcs.252973; PMC: PMC7710011 WTSIi002-A 2020-11-25 2020-11-25 PubMed: 32938685 DOI: 10.1242/jcs.252973Associated cell lines:
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Zahumenska R, Nosal V, Smolar M, Okajcekova T, Skovierova H, Strnadel J, Halasova E
Induced Pluripotency: A Powerful Tool for In Vitro Modeling
Zahumenska R et al. Induced Pluripotency: A Powerful Tool for In Vitro Modeling. . 2020-11-24. Pubmed ID: 33255453; DOI: 10.3390/ijms21238910; PMC: PMC7727808 ORIONi001-A 2020-11-24 2020-11-24 PubMed: 33255453 DOI: 10.3390/ijms21238910Associated cell lines:
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Iosef C, Pedroza AJ, Cui JZ, Dalal AR, Arakawa M, Tashima Y, Koyano TK, Burdon G, Churovich SMP, Orrick JO, Pariani M, Fischbein MP
Quantitative proteomics reveal lineage-specific protein profiles in iPSC-derived Marfan syndrome smooth muscle cells
Iosef C et al. Quantitative proteomics reveal lineage-specific protein profiles in iPSC-derived Marfan syndrome smooth muscle cells. . 2020-11-23. Pubmed ID: 33230159; DOI: 10.1038/s41598-020-77274-w; PMC: PMC7683538 NCCDFWi001-A 2020-11-23 2020-11-23 PubMed: 33230159 DOI: 10.1038/s41598-020-77274-wAssociated cell lines:
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Rai MA, Hammonds J, Pujato M, Mayhew C, Roskin K, Spearman P
Comparative analysis of human microglial models for studies of HIV replication and pathogenesis
Rai MA et al. Comparative analysis of human microglial models for studies of HIV replication and pathogenesis. . 2020-11-19. Pubmed ID: 33213476; DOI: 10.1186/s12977-020-00544-y; PMC: PMC7678224 CUSTOMi001-A 2020-11-19 2020-11-19 PubMed: 33213476 DOI: 10.1186/s12977-020-00544-yAssociated cell lines:
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Minn KT, Fu YC, He S, Dietmann S, George SC, Anastasio MA, Morris SA, Solnica-Krezel L
High-resolution transcriptional and morphogenetic profiling of cells from micropatterned human ESC gastruloid cultures
Minn KT et al. High-resolution transcriptional and morphogenetic profiling of cells from micropatterned human ESC gastruloid cultures. . 2020-11-18. Pubmed ID: 33206048; DOI: 10.7554/elife.59445; PMC: PMC7728446 WAe001-AWAe009-A 2020-11-18 2020-11-18 PubMed: 33206048 DOI: 10.7554/elife.59445 -
Arroyave F, Montaño D, Lizcano F
Diabetes Mellitus Is a Chronic Disease that Can Benefit from Therapy with Induced Pluripotent Stem Cells
Arroyave F et al. Diabetes Mellitus Is a Chronic Disease that Can Benefit from Therapy with Induced Pluripotent Stem Cells. . 2020-11-18. Pubmed ID: 33217903; DOI: 10.3390/ijms21228685; PMC: PMC7698772 IISHDOi006-A 2020-11-18 2020-11-18 PubMed: 33217903 DOI: 10.3390/ijms21228685Associated cell lines:
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Hall-Roberts H, Agarwal D, Obst J, Smith TB, Monzón-Sandoval J, Di Daniel E, Webber C, James WS, Mead E, Davis JB, Cowley SA
TREM2 Alzheimer's variant R47H causes similar transcriptional dysregulation to knockout, yet only subtle functional phenotypes in human iPSC-derived macrophages
Hall-Roberts H et al. TREM2 Alzheimer's variant R47H causes similar transcriptional dysregulation to knockout, yet only subtle functional phenotypes in human iPSC-derived macrophages. . 2020-11-16. Pubmed ID: 33198789; DOI: 10.1186/s13195-020-00709-z; PMC: PMC7667762 BIONi010-CBIONi010-C-7BIONi010-C-17 2020-11-16 2020-11-16 PubMed: 33198789 DOI: 10.1186/s13195-020-00709-zAssociated cell lines:
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Zhang L, Xu M, Ren Q, Liu G, Meng S, Xiahou K, Zhang Y, Jiang N, Zhou W
Human Induced Pluripotent Stem Cell-Derived Neural Cells from Alzheimer's Disease Patients Exhibited Different Susceptibility to Oxidative Stress
Zhang L et al. Human Induced Pluripotent Stem Cell-Derived Neural Cells from Alzheimer's Disease Patients Exhibited Different Susceptibility to Oxidative Stress. . 2020-11-15. Pubmed ID: 32988331; DOI: 10.1089/scd.2020.0103 IPTi001-A 2020-11-15 2020-11-15 PubMed: 32988331 DOI: 10.1089/scd.2020.0103Associated cell lines:
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Netsrithong R, Suwanpitak S, Boonkaew B, Trakarnsanga K, Chang LJ, Tipgomut C, Vatanashevanopakorn C, Pattanapanyasat K, Wattanapanitch M
Multilineage differentiation potential of hematoendothelial progenitors derived from human induced pluripotent stem cells
Netsrithong R et al. Multilineage differentiation potential of hematoendothelial progenitors derived from human induced pluripotent stem cells. . 2020-11-11. Pubmed ID: 33176890; DOI: 10.1186/s13287-020-01997-w; PMC: PMC7659123 MUSIi001-AMUSIi011-AMUSIi011-B 2020-11-11 2020-11-11 PubMed: 33176890 DOI: 10.1186/s13287-020-01997-wAssociated cell lines:
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Wasmus C, Dudek J
Metabolic Alterations Caused by Defective Cardiolipin Remodeling in Inherited Cardiomyopathies
Wasmus C et al. Metabolic Alterations Caused by Defective Cardiolipin Remodeling in Inherited Cardiomyopathies. . 2020-11-11. Pubmed ID: 33187128; DOI: 10.3390/life10110277; PMC: PMC7697959 LIBUCi001-ALIBUCi002-AJMUi001-AJMUi001-A-1 2020-11-11 2020-11-11 PubMed: 33187128 DOI: 10.3390/life10110277Associated cell lines:
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Giacomoni J, Bruzelius A, Stamouli CA, Rylander Ottosson D
Direct Conversion of Human Stem Cell-Derived Glial Progenitor Cells into GABAergic Interneurons
Giacomoni J et al. Direct Conversion of Human Stem Cell-Derived Glial Progenitor Cells into GABAergic Interneurons. . 2020-11-10. Pubmed ID: 33182669; DOI: 10.3390/cells9112451; PMC: PMC7698048 RCe021-A 2020-11-10 2020-11-10 PubMed: 33182669 DOI: 10.3390/cells9112451Associated cell lines:
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Zanin M, Santos BFR, Antony PMA, Berenguer-Escuder C, Larsen SB, Hanss Z, Barbuti PA, Baumuratov AS, Grossmann D, Capelle CM, Weber J, Balling R, Ollert M, Krüger R, Diederich NJ, He FQ
Mitochondria interaction networks show altered topological patterns in Parkinson's disease
Zanin M et al. Mitochondria interaction networks show altered topological patterns in Parkinson's disease. . 2020-11-10. Pubmed ID: 33173039; DOI: 10.1038/s41540-020-00156-4; PMC: PMC7655803 LCSBi001-A 2020-11-10 2020-11-10 PubMed: 33173039 DOI: 10.1038/s41540-020-00156-4Associated cell lines:
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Malankhanova T, Suldina L, Grigor'eva E, Medvedev S, Minina J, Morozova K, Kiseleva E, Zakian S, Malakhova A
A Human Induced Pluripotent Stem Cell-Derived Isogenic Model of Huntington's Disease Based on Neuronal Cells Has Several Relevant Phenotypic Abnormalities
Malankhanova T et al. A Human Induced Pluripotent Stem Cell-Derived Isogenic Model of Huntington's Disease Based on Neuronal Cells Has Several Relevant Phenotypic Abnormalities. . 2020-11-09. Pubmed ID: 33182269; DOI: 10.3390/jpm10040215; PMC: PMC7712151 ICGi007-A 2020-11-09 2020-11-09 PubMed: 33182269 DOI: 10.3390/jpm10040215Associated cell lines:
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Zhao J, Fu Y, Yamazaki Y, Ren Y, Davis MD, Liu CC, Lu W, Wang X, Chen K, Cherukuri Y, Jia L, Martens YA, Job L, Shue F, Nguyen TT, Younkin SG, Graff-Radford NR, Wszolek ZK, Brafman DA, Asmann YW, Ertekin-Taner N, Kanekiyo T, Bu G
APOE4 exacerbates synapse loss and neurodegeneration in Alzheimer's disease patient iPSC-derived cerebral organoids
Zhao J et al. APOE4 exacerbates synapse loss and neurodegeneration in Alzheimer's disease patient iPSC-derived cerebral organoids. . 2020-11-02. Pubmed ID: 33139712; DOI: 10.1038/s41467-020-19264-0; PMC: PMC7608683 ASUi001-AASUi002-AASUi005-AASUi006-A 2020-11-02 2020-11-02 PubMed: 33139712 DOI: 10.1038/s41467-020-19264-0 -
Sriram D, Chintala R, Parthasaradhi BVV, Nayak SC, Mariappan I, Radha V
Expression of a novel brain specific isoform of C3G is regulated during development
Sriram D et al. Expression of a novel brain specific isoform of C3G is regulated during development. . 2020-11-02. Pubmed ID: 33139841; DOI: 10.1038/s41598-020-75813-z; PMC: PMC7606606 LVPEIi001-A 2020-11-02 2020-11-02 PubMed: 33139841 DOI: 10.1038/s41598-020-75813-zAssociated cell lines:
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Feng B, Xu P, He Y
Novel Targets in Glucose Homeostasis and Obesity-Lesson from Rare Mutations
Feng B et al. Novel Targets in Glucose Homeostasis and Obesity-Lesson from Rare Mutations. . 2020-10-31. Pubmed ID: 33128381; DOI: 10.1007/s11892-020-01351-7 PUMCHi001-A 2020-10-31 2020-10-31 PubMed: 33128381 DOI: 10.1007/s11892-020-01351-7Associated cell lines:
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Arber C, Toombs J, Lovejoy C, Ryan NS, Paterson RW, Willumsen N, Gkanatsiou E, Portelius E, Blennow K, Heslegrave A, Schott JM, Hardy J, Lashley T, Fox NC, Zetterberg H, Wray S
Familial Alzheimer's disease patient-derived neurons reveal distinct mutation-specific effects on amyloid beta
Arber C et al. Familial Alzheimer's disease patient-derived neurons reveal distinct mutation-specific effects on amyloid beta. . 2020-11-00. Pubmed ID: 30980041; DOI: 10.1038/s41380-019-0410-8; PMC: PMC7577860 RBi001-A 2020-11-00 2020-11-00 PubMed: 30980041 DOI: 10.1038/s41380-019-0410-8Associated cell lines:
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Almazni I, Stapley RJ, Khan AO, Morgan NV
A comprehensive bioinformatic analysis of 126 patients with an inherited platelet disorder to identify both sequence and copy number genetic variants
Almazni I et al. A comprehensive bioinformatic analysis of 126 patients with an inherited platelet disorder to identify both sequence and copy number genetic variants. . 2020-11-00. Pubmed ID: 32935436; DOI: 10.1002/humu.24114 GENYOi005-A 2020-11-00 2020-11-00 PubMed: 32935436 DOI: 10.1002/humu.24114Associated cell lines:
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Lauschke K, Rosenmai AK, Meiser I, Neubauer JC, Schmidt K, Rasmussen MA, Holst B, Taxvig C, Emnéus JK, Vinggaard AM
A novel human pluripotent stem cell-based assay to predict developmental toxicity
Lauschke K et al. A novel human pluripotent stem cell-based assay to predict developmental toxicity. . 2020-11-00. Pubmed ID: 32700165; DOI: 10.1007/s00204-020-02856-6; PMC: PMC7603451 BIONi010-C 2020-11-00 2020-11-00 PubMed: 32700165 DOI: 10.1007/s00204-020-02856-6Associated cell lines:
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McNeill RV, Ziegler GC, Radtke F, Nieberler M, Lesch KP, Kittel-Schneider S
Mental health dished up-the use of iPSC models in neuropsychiatric research
McNeill RV et al. Mental health dished up-the use of iPSC models in neuropsychiatric research. . 2020-11-00. Pubmed ID: 32377792; DOI: 10.1007/s00702-020-02197-9; PMC: PMC7578166 TUSMi004-ATUSMi005-A 2020-11-00 2020-11-00 PubMed: 32377792 DOI: 10.1007/s00702-020-02197-9Associated cell lines:
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Zhang X, Thompson JA, Zhang D, Charng J, Arunachalam S, McLaren TL, Lamey TM, De Roach JN, Jennings L, McLenachan S, Chen FK
Characterization of CRB1 splicing in retinal organoids derived from a patient with adult-onset rod-cone dystrophy caused by the c.1892A>G and c.2548G>A variants
Zhang X et al. Characterization of CRB1 splicing in retinal organoids derived from a patient with adult-onset rod-cone dystrophy caused by the c.1892A>G and c.2548G>A variants. . 2020-11-00. Pubmed ID: 32931148; DOI: 10.1002/mgg3.1489; PMC: PMC7667350 LEIi005-ALEIi006-A 2020-11-00 2020-11-00 PubMed: 32931148 DOI: 10.1002/mgg3.1489 -
Xue VW, Wong SCC, Cho WCS
Genome-wide CRISPR screens for the identification of therapeutic targets for cancer treatment
Xue VW et al. Genome-wide CRISPR screens for the identification of therapeutic targets for cancer treatment. . 2020-11-00. Pubmed ID: 32893711; DOI: 10.1080/14728222.2020.1820986 WAe001-AWAe001-A-2 2020-11-00 2020-11-00 PubMed: 32893711 DOI: 10.1080/14728222.2020.1820986Associated cell lines:
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Freude KK, Saruhanian S, McCauley A, Paterson C, Odette M, Oostenink A, Hyttel P, Gillies M, Haukedal H, Kolko M
Enrichment of retinal ganglion and Müller glia progenitors from retinal organoids derived from human induced pluripotent stem cells - possibilities and current limitations
Freude KK et al. Enrichment of retinal ganglion and Müller glia progenitors from retinal organoids derived from human induced pluripotent stem cells - possibilities and current limitations. . 2020-10-26. Pubmed ID: 33178399; DOI: 10.4252/wjsc.v12.i10.1171; PMC: PMC7596448 BIONi010-CBIONi010-C-19 2020-10-26 2020-10-26 PubMed: 33178399 DOI: 10.4252/wjsc.v12.i10.1171Associated cell lines:
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Cozzitorto C, Mueller L, Ruzittu S, Mah N, Willnow D, Darrigrand JF, Wilson H, Khosravinia D, Mahmoud AA, Risolino M, Selleri L, Spagnoli FM
A Specialized Niche in the Pancreatic Microenvironment Promotes Endocrine Differentiation
Cozzitorto C et al. A Specialized Niche in the Pancreatic Microenvironment Promotes Endocrine Differentiation. . 2020-10-26. Pubmed ID: 32857951; DOI: 10.1016/j.devcel.2020.08.003; PMC: PMC7720791 BIHi005-AHMGUi001-A 2020-10-26 2020-10-26 PubMed: 32857951 DOI: 10.1016/j.devcel.2020.08.003Associated cell lines:
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Ponomarenko M, Sharypova E, Drachkova I, Chadaeva I, Arkova O, Podkolodnaya O, Ponomarenko P, Kolchanov N, Savinkova L
Unannotated single nucleotide polymorphisms in the TATA box of erythropoiesis genes show in vitro positive involvements in cognitive and mental disorders
Ponomarenko M et al. Unannotated single nucleotide polymorphisms in the TATA box of erythropoiesis genes show in vitro positive involvements in cognitive and mental disorders. . 2020-10-22. Pubmed ID: 33092544; DOI: 10.1186/s12881-020-01106-x; PMC: PMC7579878 ICGi007-A 2020-10-22 2020-10-22 PubMed: 33092544 DOI: 10.1186/s12881-020-01106-xAssociated cell lines:
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Benetó N, Vilageliu L, Grinberg D, Canals I
Sanfilippo Syndrome: Molecular Basis, Disease Models and Therapeutic Approaches
Benetó N et al. Sanfilippo Syndrome: Molecular Basis, Disease Models and Therapeutic Approaches. . 2020-10-22. Pubmed ID: 33105639; DOI: 10.3390/ijms21217819; PMC: PMC7659972 IMEDEAi004-AIMEDEAi004-BTRNDi006-A 2020-10-22 2020-10-22 PubMed: 33105639 DOI: 10.3390/ijms21217819Associated cell lines:
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Madsen A, Höppner G, Krause J, Hirt MN, Laufer SD, Schweizer M, Tan WLW, Mosqueira D, Anene-Nzelu CG, Lim I, Foo RSY, Hansen A, Eschenhagen T, Stenzig J
An Important Role for DNMT3A-Mediated DNA Methylation in Cardiomyocyte Metabolism and Contractility
Madsen A et al. An Important Role for DNMT3A-Mediated DNA Methylation in Cardiomyocyte Metabolism and Contractility. . 2020-10-20. Pubmed ID: 32885664; DOI: 10.1161/circulationaha.119.044444; PMC: PMC7566310 UKEi003-C 2020-10-20 2020-10-20 PubMed: 32885664 DOI: 10.1161/circulationaha.119.044444Associated cell lines:
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Umezawa A, Sato Y, Kusakawa S, Amagase R, Akutsu H, Nakamura K, Kasahara M, Matsubara Y, Igarashi T
Research and Development Strategy for Future Embryonic Stem Cell-Based Therapy in Japan
Umezawa A et al. Research and Development Strategy for Future Embryonic Stem Cell-Based Therapy in Japan. . 2020-10-15. Pubmed ID: 33225099; DOI: 10.31662/jmaj.2018-0029; PMC: PMC7676987 KUIMSe001-AKUIMSe002-AKUIMSe003-AKUIMSe004-AKUIMSe005-AKUIMSe006-AKUIMSe007-A 2020-10-15 2020-10-15 PubMed: 33225099 DOI: 10.31662/jmaj.2018-0029Associated cell lines:
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Mannhardt I, Saleem U, Mosqueira D, Loos MF, Ulmer BM, Lemoine MD, Larsson C, Améen C, de Korte T, Vlaming MLH, Harris K, Clements P, Denning C, Hansen A, Eschenhagen T
Comparison of 10 Control hPSC Lines for Drug Screening in an Engineered Heart Tissue Format
Mannhardt I et al. Comparison of 10 Control hPSC Lines for Drug Screening in an Engineered Heart Tissue Format. . 2020-10-13. Pubmed ID: 33053362; DOI: 10.1016/j.stemcr.2020.09.002; PMC: PMC7561618 UKEi003-C 2020-10-13 2020-10-13 PubMed: 33053362 DOI: 10.1016/j.stemcr.2020.09.002Associated cell lines:
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Sumer SA, Hoffmann S, Laue S, Campbell B, Raedecke K, Frajs V, Clauss S, Kääb S, Janssen JWG, Jauch A, Laugwitz KL, Dorn T, Moretti A, Rappold GA
Precise Correction of Heterozygous SHOX2 Mutations in hiPSCs Derived from Patients with Atrial Fibrillation via Genome Editing and Sib Selection
Sumer SA et al. Precise Correction of Heterozygous SHOX2 Mutations in hiPSCs Derived from Patients with Atrial Fibrillation via Genome Editing and Sib Selection. . 2020-10-13. Pubmed ID: 32976766; DOI: 10.1016/j.stemcr.2020.08.015; PMC: PMC7562944 MRIi016-AMRIi024-AMRIi016-A-1 2020-10-13 2020-10-13 PubMed: 32976766 DOI: 10.1016/j.stemcr.2020.08.015Associated cell lines:
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Nolbrant S, Giacomoni J, Hoban DB, Bruzelius A, Birtele M, Chandler-Militello D, Pereira M, Ottosson DR, Goldman SA, Parmar M
Direct Reprogramming of Human Fetal- and Stem Cell-Derived Glial Progenitor Cells into Midbrain Dopaminergic Neurons
Nolbrant S et al. Direct Reprogramming of Human Fetal- and Stem Cell-Derived Glial Progenitor Cells into Midbrain Dopaminergic Neurons. . 2020-10-13. Pubmed ID: 32976765; DOI: 10.1016/j.stemcr.2020.08.013; PMC: PMC7562948 RCe021-AKIe055-A 2020-10-13 2020-10-13 PubMed: 32976765 DOI: 10.1016/j.stemcr.2020.08.013 -
Ast J, Arvaniti A, Fine NHF, Nasteska D, Ashford FB, Stamataki Z, Koszegi Z, Bacon A, Jones BJ, Lucey MA, Sasaki S, Brierley DI, Hastoy B, Tomas A, D'Agostino G, Reimann F, Lynn FC, Reissaus CA, Linnemann AK, D'Este E, Calebiro D, Trapp S, Johnsson K, Podewin T, Broichhagen J, Hodson DJ
Author Correction: Super-resolution microscopy compatible fluorescent probes reveal endogenous glucagon-like peptide-1 receptor distribution and dynamics
Ast J et al. Author Correction: Super-resolution microscopy compatible fluorescent probes reveal endogenous glucagon-like peptide-1 receptor distribution and dynamics. . 2020-10-09. Pubmed ID: 33037231; DOI: 10.1038/s41467-020-19101-4; PMC: PMC7547653 WAe001-A 2020-10-09 2020-10-09 PubMed: 33037231 DOI: 10.1038/s41467-020-19101-4Associated cell lines:
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Grigor'eva EV, Malankhanova TB, Surumbayeva A, Pavlova SV, Minina JM, Kizilova EA, Suldina LA, Morozova KN, Kiseleva E, Sorokoumov ED, Lebedev IN, Zakian SM, Malakhova AA
Generation of GABAergic striatal neurons by a novel iPSC differentiation protocol enabling scalability and cryopreservation of progenitor cells
Grigor'eva EV et al. Generation of GABAergic striatal neurons by a novel iPSC differentiation protocol enabling scalability and cryopreservation of progenitor cells. . 2020-10-00. Pubmed ID: 32519278; DOI: 10.1007/s10616-020-00406-7; PMC: PMC7547944 ICGi007-A 2020-10-00 2020-10-00 PubMed: 32519278 DOI: 10.1007/s10616-020-00406-7Associated cell lines:
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Xia S, Wang X, Yue P, Li Y, Zhang D
Establishment of induced pluripotent stem cell lines from a family of an ARVC patient receiving heart transplantation in infant age carrying compound heterozygous mutations in DSP gene
Xia S et al. Establishment of induced pluripotent stem cell lines from a family of an ARVC patient receiving heart transplantation in infant age carrying compound heterozygous mutations in DSP gene. . 2020-10-00. Pubmed ID: 32942234; DOI: 10.1016/j.scr.2020.101977 HUBUi001-AHUBUi002-AHUBUi003-A 2020-10-00 2020-10-00 PubMed: 32942234 DOI: 10.1016/j.scr.2020.101977Associated cell lines:
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Sequiera GL, Rockman-Greenberg C, Dhingra S
Establishment of variant free-iPSC (UOMi003-A) line from patient with mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes
Sequiera GL et al. Establishment of variant free-iPSC (UOMi003-A) line from patient with mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes. . 2020-10-00. Pubmed ID: 32777772; DOI: 10.1016/j.scr.2020.101935 UOMi003-A 2020-10-00 2020-10-00 PubMed: 32777772 DOI: 10.1016/j.scr.2020.101935Associated cell lines:
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Zhou D, Sun Y, Shen J, Su J, Gong T, Jiang C, Liang P
Generation of an induced pluripotent stem cell line from the dermal fibroblasts of a patient with arrhythmogenic right ventricular cardiomyopathy carrying a PKP2/c.2489 + 1G > A mutation
Zhou D et al. Generation of an induced pluripotent stem cell line from the dermal fibroblasts of a patient with arrhythmogenic right ventricular cardiomyopathy carrying a PKP2/c.2489 + 1G > A mutation. . 2020-10-00. Pubmed ID: 32916635; DOI: 10.1016/j.scr.2020.101965 ZJUi004-A 2020-10-00 2020-10-00 PubMed: 32916635 DOI: 10.1016/j.scr.2020.101965Associated cell lines:
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Chen M, Maimaitili M, Habekost M, Gill KP, Mermet-Joret N, Nabavi S, Febbraro F, Denham M
Rapid generation of regionally specified CNS neurons by sequential patterning and conversion of human induced pluripotent stem cells
Chen M et al. Rapid generation of regionally specified CNS neurons by sequential patterning and conversion of human induced pluripotent stem cells. . 2020-10-00. Pubmed ID: 32791483; DOI: 10.1016/j.scr.2020.101945 DANi001-CDANi002-CDANi003-HDANi004-ADANi005-ADANi006-FDANi007-ADANi008-FDANi009-CDANi010-ADANi011-A 2020-10-00 2020-10-00 PubMed: 32791483 DOI: 10.1016/j.scr.2020.101945 -
Strnadel J, Zahumenska R, Nosal V, Smolar M, Marcinek J, Kalman M, Juhas S, Juhasova J, Studenovska H, Dumortier H, Chromec T, Skovierova H, Mitruskova B, Kapralik I, Mersakova S, Brany D, Halasova E
Generation of ORIONi001-A induced pluripotent stem cell line for in vitro modeling of sporadic form of amyotrophic lateral sclerosis
Strnadel J et al. Generation of ORIONi001-A induced pluripotent stem cell line for in vitro modeling of sporadic form of amyotrophic lateral sclerosis. . 2020-10-00. Pubmed ID: 32919353; DOI: 10.1016/j.scr.2020.101981 ORIONi001-A 2020-10-00 2020-10-00 PubMed: 32919353 DOI: 10.1016/j.scr.2020.101981Associated cell lines:
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Cosset E, Vannary T, Sloan-Béna F, Gimelli S, Gerstel E, Krause KH, Marteyn A
Generation of human induced pluripotent stem cell line UNIGEi003-A from skin fibroblasts of an apparently healthy male donor
Cosset E et al. Generation of human induced pluripotent stem cell line UNIGEi003-A from skin fibroblasts of an apparently healthy male donor. . 2020-10-00. Pubmed ID: 32805538; DOI: 10.1016/j.scr.2020.101928 UNIGEi003-A 2020-10-00 2020-10-00 PubMed: 32805538 DOI: 10.1016/j.scr.2020.101928Associated cell lines:
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Ababneh NA, Ali D, Barham R, Al-Kurdi B, Sharar N, Al Hadidi S, Qanno' O, Ryalat AT, Salah B, Awidi A
Establishment of a human induced pluripotent stem cell line, JUCTCi012-A, from multiple symmetric lipomatosis (MSL) patient carrying a homozygous Arg707Trp (c.2119C > T) mutation in the MFN2 gene
Ababneh NA et al. Establishment of a human induced pluripotent stem cell line, JUCTCi012-A, from multiple symmetric lipomatosis (MSL) patient carrying a homozygous Arg707Trp (c.2119C > T) mutation in the MFN2 gene. . 2020-10-00. Pubmed ID: 32916636; DOI: 10.1016/j.scr.2020.101967 JUCTCi012-A 2020-10-00 2020-10-00 PubMed: 32916636 DOI: 10.1016/j.scr.2020.101967Associated cell lines:
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Kamand M, Ilieva M, Louise Forsberg S, Thomassen M, Meyer M, Fex Svenningsen Å, Maria Michel T
Derivation of induced pluripotent stem cells (SDUKIi003-A) from a 20-year-old male patient diagnosed with Asperger syndrome
Kamand M et al. Derivation of induced pluripotent stem cells (SDUKIi003-A) from a 20-year-old male patient diagnosed with Asperger syndrome. . 2020-10-00. Pubmed ID: 32916638; DOI: 10.1016/j.scr.2020.101974 SDUKIi002-ASDUKIi003-A 2020-10-00 2020-10-00 PubMed: 32916638 DOI: 10.1016/j.scr.2020.101974Associated cell lines:
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Lee M, Choi NY, Park S, Bang JS, Lee Y, Jeong D, Ham S, Lim S, Kim KH, Ko K
Generation of OCT4-EGFP, NANOG-tdTomato dual reporter human induced pluripotent stem cell line, KKUi001-A, using the CRISPR/Cas9 system
Lee M et al. Generation of OCT4-EGFP, NANOG-tdTomato dual reporter human induced pluripotent stem cell line, KKUi001-A, using the CRISPR/Cas9 system. . 2020-10-00. Pubmed ID: 32777770; DOI: 10.1016/j.scr.2020.101943 BCRTi001-AKKUi001-A 2020-10-00 2020-10-00 PubMed: 32777770 DOI: 10.1016/j.scr.2020.101943Associated cell lines:
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Zhao Q, Cui Y, Wang J, Shi L, Qi Z, Luan J, Zhang Y, Zhou X, Han J
Development of a human iPSC line (SMBCi004-A) from a patient with Gaucher disease
Zhao Q et al. Development of a human iPSC line (SMBCi004-A) from a patient with Gaucher disease. . 2020-10-00. Pubmed ID: 32977293; DOI: 10.1016/j.scr.2020.101989 SMBCi004-A 2020-10-00 2020-10-00 PubMed: 32977293 DOI: 10.1016/j.scr.2020.101989Associated cell lines:
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Milagre I, Pereira C, Oliveira RA, Jansen LET
Reprogramming of human cells to pluripotency induces CENP-A chromatin depletion
Milagre I et al. Reprogramming of human cells to pluripotency induces CENP-A chromatin depletion. . 2020-10-00. Pubmed ID: 33081635; DOI: 10.1098/rsob.200227; PMC: PMC7653353 WAe009-A 2020-10-00 2020-10-00 PubMed: 33081635 DOI: 10.1098/rsob.200227Associated cell lines:
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Ratnavadivel S, Szymanski de Toledo M, Rasmussen TB, Šarić T, Gummert J, Zenke M, Milting H
Human pluripotent stem cell line (HDZi001-A) derived from a patient carrying the ARVC-5 associated mutation TMEM43-p.S358L
Ratnavadivel S et al. Human pluripotent stem cell line (HDZi001-A) derived from a patient carrying the ARVC-5 associated mutation TMEM43-p.S358L. . 2020-10-00. Pubmed ID: 32858485; DOI: 10.1016/j.scr.2020.101957 HDZi001-A 2020-10-00 2020-10-00 PubMed: 32858485 DOI: 10.1016/j.scr.2020.101957Associated cell lines:
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Banal C, Quelennec E, Bertani-Torres W, Gacem N, Amiel J, Marlin S, Petit F, Pingault V, Lefort N, Bondurand N
Generation of an iPSC line (IMAGINi022-A) from a patient carrying a SOX10 missense mutation and presenting with deafness, depigmentation and progressive neurological impairment
Banal C et al. Generation of an iPSC line (IMAGINi022-A) from a patient carrying a SOX10 missense mutation and presenting with deafness, depigmentation and progressive neurological impairment. . 2020-10-00. Pubmed ID: 32795927; DOI: 10.1016/j.scr.2020.101936 IMAGINi022-A 2020-10-00 2020-10-00 PubMed: 32795927 DOI: 10.1016/j.scr.2020.101936Associated cell lines:
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Vaidyanath A, Khan M, Vaishnav B, Kakrani AL, Patil S, Shiras A
Establishment of integration free iPSC clones, NCCSi011-A and NCCSi011-B from a liver cirrhosis patient of Indian origin with hepatic encephalopathy
Vaidyanath A et al. Establishment of integration free iPSC clones, NCCSi011-A and NCCSi011-B from a liver cirrhosis patient of Indian origin with hepatic encephalopathy. . 2020-10-00. Pubmed ID: 32971460; DOI: 10.1016/j.scr.2020.101992 NCCSi010-ANCCSi010-B 2020-10-00 2020-10-00 PubMed: 32971460 DOI: 10.1016/j.scr.2020.101992Associated cell lines:
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Lu JZ, Zhang L, Zhu HY, Qi YY, Bai ZH, Jia WW, Liu ZM
An induced pluripotent stem cell line (EHTJUi002-A) derived from a neonate with c.678G>A mutation in the gene FZD4 causing exudative vitreoretinopathy
Lu JZ et al. An induced pluripotent stem cell line (EHTJUi002-A) derived from a neonate with c.678G>A mutation in the gene FZD4 causing exudative vitreoretinopathy. . 2020-10-00. Pubmed ID: 32889247; DOI: 10.1016/j.scr.2020.101932 EHTJUi002-A 2020-10-00 2020-10-00 PubMed: 32889247 DOI: 10.1016/j.scr.2020.101932Associated cell lines:
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Kido J, Nakamura K, Era T
Role of induced pluripotent stem cells in lysosomal storage diseases
Kido J et al. Role of induced pluripotent stem cells in lysosomal storage diseases. . 2020-10-00. Pubmed ID: 32828964; DOI: 10.1016/j.mcn.2020.103540 TRNDi006-ATRNDi001-DUNIGEi001-A 2020-10-00 2020-10-00 PubMed: 32828964 DOI: 10.1016/j.mcn.2020.103540Associated cell lines:
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Jamwal VS, Vishnu VV, Domreddy A, Parekh Y, Kumar BK, Chandra Shekar P, Singh S
Generation of iPSC from fetal fibroblast cells obtained from an abortus with type-I tri-allelic variants
Jamwal VS et al. Generation of iPSC from fetal fibroblast cells obtained from an abortus with type-I tri-allelic variants. . 2020-10-00. Pubmed ID: 32916634; DOI: 10.1016/j.scr.2020.101963 CCMBi001-A 2020-10-00 2020-10-00 PubMed: 32916634 DOI: 10.1016/j.scr.2020.101963Associated cell lines:
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Yoshida S, Okura H, Suga H, Soen M, Kawaguchi Y, Kurimoto J, Miyata T, Takagi H, Arima H, Fujikawa T, Otsuka F, Matsuyama A
Generation of four induced pluripotent stem cell lines (FHUi003-A, FHUi003-B, FHUi004-A and FHUi004-B) from two affected individuals of a familial neurohypophyseal diabetes insipidus family
Yoshida S et al. Generation of four induced pluripotent stem cell lines (FHUi003-A, FHUi003-B, FHUi004-A and FHUi004-B) from two affected individuals of a familial neurohypophyseal diabetes insipidus family. . 2020-10-00. Pubmed ID: 32927425; DOI: 10.1016/j.scr.2020.101960 FHUi003-AFHUi003-BFHUi004-AFHUi004-B 2020-10-00 2020-10-00 PubMed: 32927425 DOI: 10.1016/j.scr.2020.101960 -
Sequiera GL, Rockman-Greenberg C, Dhingra S
Generation of human induced pluripotent stem cell (hiPSC) line UOMi001-A from a patient with Leigh-like syndrome harbouring compound heterozygous variants in ECHS1 gene
Sequiera GL et al. Generation of human induced pluripotent stem cell (hiPSC) line UOMi001-A from a patient with Leigh-like syndrome harbouring compound heterozygous variants in ECHS1 gene. . 2020-10-00. Pubmed ID: 32777769; DOI: 10.1016/j.scr.2020.101934 UOMi001-A 2020-10-00 2020-10-00 PubMed: 32777769 DOI: 10.1016/j.scr.2020.101934Associated cell lines:
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Malakhova AA, Grigor'eva EV, Pavlova SV, Malankhanova TB, Valetdinova KR, Vyatkin YV, Khabarova EA, Rzaev JA, Zakian SM, Medvedev SP
Generation of induced pluripotent stem cell lines ICGi021-A and ICGi022-A from peripheral blood mononuclear cells of two healthy individuals from Siberian population
Malakhova AA et al. Generation of induced pluripotent stem cell lines ICGi021-A and ICGi022-A from peripheral blood mononuclear cells of two healthy individuals from Siberian population. . 2020-10-00. Pubmed ID: 32805537; DOI: 10.1016/j.scr.2020.101952 ICGi015-AICGi015-BICGi021-AICGi022-A 2020-10-00 2020-10-00 PubMed: 32805537 DOI: 10.1016/j.scr.2020.101952 -
Schoger E, Argyriou L, Zimmermann WH, Cyganek L, Zelarayán LC
Generation of homozygous CRISPRa human induced pluripotent stem cell (hiPSC) lines for sustained endogenous gene activation
Schoger E et al. Generation of homozygous CRISPRa human induced pluripotent stem cell (hiPSC) lines for sustained endogenous gene activation. . 2020-10-00. Pubmed ID: 33038615; DOI: 10.1016/j.scr.2020.101944 RUCDRi002-ARUCDRi002-A-5 2020-10-00 2020-10-00 PubMed: 33038615 DOI: 10.1016/j.scr.2020.101944Associated cell lines:
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Zlotnik D, Rabinski T, Ofir R, Hershkovitz E, Vatine GD
Generation of iPSC lines from two (BGUi002-A and BGUi003-A) homozygous p450 oxidoreductase-deficient patients and from one (BGUi001-A) heterozygous healthy family relative
Zlotnik D et al. Generation of iPSC lines from two (BGUi002-A and BGUi003-A) homozygous p450 oxidoreductase-deficient patients and from one (BGUi001-A) heterozygous healthy family relative. . 2020-10-00. Pubmed ID: 32905996; DOI: 10.1016/j.scr.2020.101975 BGUi001-ABGUi002-ABGUi003-ABGUi004-ABGUi005-A 2020-10-00 2020-10-00 PubMed: 32905996 DOI: 10.1016/j.scr.2020.101975 -
Kondrateva E, Adilgereeva E, Amelina E, Tabakov V, Demchenko A, Ustinov K, Yasinovsky M, Voronina E, Lavrov A, Smirnikhina S
Generation of induced pluripotent stem cell line (RCMGi001-A) from human skin fibroblasts of a cystic fibrosis patient with p.F508del mutation
Kondrateva E et al. Generation of induced pluripotent stem cell line (RCMGi001-A) from human skin fibroblasts of a cystic fibrosis patient with p.F508del mutation. . 2020-10-00. Pubmed ID: 32777768; DOI: 10.1016/j.scr.2020.101933 RCMGi001-A 2020-10-00 2020-10-00 PubMed: 32777768 DOI: 10.1016/j.scr.2020.101933Associated cell lines:
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Kim MJ, Lee EY, You YH, Yang HK, Yoon KH, Kim JW
Generation of iPSC-derived insulin-producing cells from patients with type 1 and type 2 diabetes compared with healthy control
Kim MJ et al. Generation of iPSC-derived insulin-producing cells from patients with type 1 and type 2 diabetes compared with healthy control. . 2020-10-00. Pubmed ID: 32882526; DOI: 10.1016/j.scr.2020.101958 CMCi003-ACMCi004-ACMCi005-A 2020-10-00 2020-10-00 PubMed: 32882526 DOI: 10.1016/j.scr.2020.101958 -
Gao X, Qiu SW, Feng ML, Huang SS, Kang DY, Han MY, Dai P, Yuan YY
Establishment of human induced pluripotent stem cell line (CPGHi002-A) from a 10-month-old female patient with DDOD syndrome carrying a heterozygous c.1516 C > T mutation in ATP6V1B2
Gao X et al. Establishment of human induced pluripotent stem cell line (CPGHi002-A) from a 10-month-old female patient with DDOD syndrome carrying a heterozygous c.1516 C > T mutation in ATP6V1B2. . 2020-10-00. Pubmed ID: 32961450; DOI: 10.1016/j.scr.2020.101986 CPGHi002-A 2020-10-00 2020-10-00 PubMed: 32961450 DOI: 10.1016/j.scr.2020.101986Associated cell lines:
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Liu S, Niu S, Li Y, Xiong H, Li Y, Jian L, Zhang L
Establishment of an induced pluripotent stem cell line (ZZUSAHi002-A) derived from peripheral blood mononuclear cells of a healthy individual
Liu S et al. Establishment of an induced pluripotent stem cell line (ZZUSAHi002-A) derived from peripheral blood mononuclear cells of a healthy individual. . 2020-10-00. Pubmed ID: 32911326; DOI: 10.1016/j.scr.2020.101966 ZZUSAHi002-A 2020-10-00 2020-10-00 PubMed: 32911326 DOI: 10.1016/j.scr.2020.101966Associated cell lines:
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Sequiera GL, Rockman-Greenberg C, Dhingra S
Induced pluripotent stem cell line UOMi002-A from a patient with Leigh syndrome with compound heterozygous mutations in the NDUFV1 gene
Sequiera GL et al. Induced pluripotent stem cell line UOMi002-A from a patient with Leigh syndrome with compound heterozygous mutations in the NDUFV1 gene. . 2020-10-00. Pubmed ID: 32871395; DOI: 10.1016/j.scr.2020.101964 UOMi002-A 2020-10-00 2020-10-00 PubMed: 32871395 DOI: 10.1016/j.scr.2020.101964Associated cell lines:
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Pournasr B, Duncan SA
Generation of isogenic Propionyl-CoA carboxylase beta subunit (PCCB) deficient induced pluripotent stem cell lines
Pournasr B et al. Generation of isogenic Propionyl-CoA carboxylase beta subunit (PCCB) deficient induced pluripotent stem cell lines. . 2020-10-00. Pubmed ID: 32822967; DOI: 10.1016/j.scr.2020.101953; PMC: PMC7640943 MUSCSDi001-AMUSCSDi001-A-1MUSCSDi001-A-2 2020-10-00 2020-10-00 PubMed: 32822967 DOI: 10.1016/j.scr.2020.101953Associated cell lines:
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Hirose S, Tanaka Y, Shibata M, Kimura Y, Ishikawa M, Higurashi N, Yamamoto T, Ichise E, Chiyonobu T, Ishii A
Application of induced pluripotent stem cells in epilepsy
Hirose S et al. Application of induced pluripotent stem cells in epilepsy. . 2020-10-00. Pubmed ID: 32758699; DOI: 10.1016/j.mcn.2020.103535 CSSi005-AFUi002-AHIHDNEi002-AHIHDNEi003-AIBCHi001-ACSSi008-A 2020-10-00 2020-10-00 PubMed: 32758699 DOI: 10.1016/j.mcn.2020.103535Associated cell lines:
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Lai LL, Chen YJ, Li YL, Lin XH, Wang MW, Dong EL, Wang N, Chen WJ, Lin X
Novel CAPN1 mutations extend the phenotypic heterogeneity in combined spastic paraplegia and ataxia
Lai LL et al. Novel CAPN1 mutations extend the phenotypic heterogeneity in combined spastic paraplegia and ataxia. . 2020-10-00. Pubmed ID: 32860341; DOI: 10.1002/acn3.51169; PMC: PMC7545613 FJMUi001-A 2020-10-00 2020-10-00 PubMed: 32860341 DOI: 10.1002/acn3.51169Associated cell lines:
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Shan H, Ye J, Hai Ping X, XinYue H, ShuYang Z
Establishment of an induced pluripotent stem cell line from a patient with hereditary transthyretin amyloidosis carrying transthyretin (TTR) mutation p.Phe53Val
Shan H et al. Establishment of an induced pluripotent stem cell line from a patient with hereditary transthyretin amyloidosis carrying transthyretin (TTR) mutation p.Phe53Val. . 2020-10-00. Pubmed ID: 32858486; DOI: 10.1016/j.scr.2020.101940 PUMCHi005-A 2020-10-00 2020-10-00 PubMed: 32858486 DOI: 10.1016/j.scr.2020.101940Associated cell lines:
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Rolova T, Wu YC, Koskuvi M, Voutilainen J, Sonninen TM, Kuusisto J, Laakso M, Hämäläinen RH, Koistinaho J, Lehtonen Š
Generation of a human induced pluripotent stem cell line (UEFi003-A) carrying heterozygous A673T variant in amyloid precursor protein associated with a reduced risk of Alzheimer's disease
Rolova T et al. Generation of a human induced pluripotent stem cell line (UEFi003-A) carrying heterozygous A673T variant in amyloid precursor protein associated with a reduced risk of Alzheimer's disease. . 2020-10-00. Pubmed ID: 32911327; DOI: 10.1016/j.scr.2020.101968 UEFi003-A 2020-10-00 2020-10-00 PubMed: 32911327 DOI: 10.1016/j.scr.2020.101968Associated cell lines:
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Dostanic Milica, Windt Laura M., Stein Jeroen M., van Meer Berend J., Bellin Milena, Orlova Valeria, Mastrangeli Massimo, Mummery Christine L., Sarro Pasqualina M.
A Miniaturized EHT Platform for Accurate Measurements of Tissue Contractile Properties
Dostanic Milica et al. A Miniaturized EHT Platform for Accurate Measurements of Tissue Contractile Properties. . 2020-10-00. DOI: 10.1109/jmems.2020.3011196 LUMCi028-A 2020-10-00 2020-10-00 DOI: 10.1109/jmems.2020.3011196Associated cell lines:
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Metzler E, Telugu N, Diecke S, Spuler S, Escobar H
Generation of three age and gender matched pairs of human induced pluripotent stem cells derived from myoblasts (MDCi011-A, MDCi012-A, MDCi013-A) and from peripheral blood mononuclear cells (MDCi011-B, MDCi012-B, MDCi013-B) from the same donor
Metzler E et al. Generation of three age and gender matched pairs of human induced pluripotent stem cells derived from myoblasts (MDCi011-A, MDCi012-A, MDCi013-A) and from peripheral blood mononuclear cells (MDCi011-B, MDCi012-B, MDCi013-B) from the same donor. . 2020-10-00. Pubmed ID: 32961449; DOI: 10.1016/j.scr.2020.101987 MDCi011-AMDCi011-BMDCi012-AMDCi012-BMDCi013-AMDCi013-B 2020-10-00 2020-10-00 PubMed: 32961449 DOI: 10.1016/j.scr.2020.101987 -
Metzler E, Telugu N, Diecke S, Spuler S, Escobar H
Generation of two human induced pluripotent stem cell lines derived from myoblasts (MDCi014-A) and from peripheral blood mononuclear cells (MDCi014-B) from the same donor
Metzler E et al. Generation of two human induced pluripotent stem cell lines derived from myoblasts (MDCi014-A) and from peripheral blood mononuclear cells (MDCi014-B) from the same donor. . 2020-10-00. Pubmed ID: 32979629; DOI: 10.1016/j.scr.2020.101998 MDCi014-AMDCi014-B 2020-10-00 2020-10-00 PubMed: 32979629 DOI: 10.1016/j.scr.2020.101998 -
Quelennec E, Banal C, Hamlin M, Clémantine D, Michael M, Lefort N
Generation of two induced pluripotent stem cell lines IMAGINi004-A and IMAGINi005-A from healthy donors
Quelennec E et al. Generation of two induced pluripotent stem cell lines IMAGINi004-A and IMAGINi005-A from healthy donors. . 2020-10-00. Pubmed ID: 32866896; DOI: 10.1016/j.scr.2020.101959 IMAGINi004-AIMAGINi005-A 2020-10-00 2020-10-00 PubMed: 32866896 DOI: 10.1016/j.scr.2020.101959Associated cell lines:
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Aqel YWA, Ali G, Elsayed AK, Al-Khawaga S, Hussain K, Abdelalim EM
Generation of two human iPSC lines from patients with maturity-onset diabetes of the young type 2 (MODY2) and permanent neonatal diabetes due to mutations in the GCK gene
Aqel YWA et al. Generation of two human iPSC lines from patients with maturity-onset diabetes of the young type 2 (MODY2) and permanent neonatal diabetes due to mutations in the GCK gene. . 2020-10-00. Pubmed ID: 32971462; DOI: 10.1016/j.scr.2020.101991 QBRIi010-AQBRIi011-A 2020-10-00 2020-10-00 PubMed: 32971462 DOI: 10.1016/j.scr.2020.101991Associated cell lines:
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Ababneh NA, Al-Kurdi B, Ali D, Barham R, Sharar N, Mrahleh MM, Salah B, Awidi A
Generation of a human induced pluripotent stem cell (iPSC) line (JUCTCi011-A) from skin fibroblasts of a healthy Jordanian male subject
Ababneh NA et al. Generation of a human induced pluripotent stem cell (iPSC) line (JUCTCi011-A) from skin fibroblasts of a healthy Jordanian male subject. . 2020-10-00. Pubmed ID: 32771906; DOI: 10.1016/j.scr.2020.101923 JUCTCi011-A 2020-10-00 2020-10-00 PubMed: 32771906 DOI: 10.1016/j.scr.2020.101923Associated cell lines:
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Liu H, Li S, Ren C, Liu W, Zhu B, Wang L, Xu H, Xie W, Zuo X, Zhou Y, Luo L, Jiang X
Generation of an ESRG Pr-tdTomato reporter human embryonic stem cell line, CSUe011-A, using CRISPR/Cas9 editing
Liu H et al. Generation of an ESRG Pr-tdTomato reporter human embryonic stem cell line, CSUe011-A, using CRISPR/Cas9 editing. . 2020-10-00. Pubmed ID: 32919352; DOI: 10.1016/j.scr.2020.101983 CSUe011-A 2020-10-00 2020-10-00 PubMed: 32919352 DOI: 10.1016/j.scr.2020.101983Associated cell lines:
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Kim KP, Yoon J, Kim J, Röpke A, Shin B, Wook Han D, Greber B, Schöler HR
Generation of a human iPSC line (MPIi007-A) from a patient with Metachromatic leukodystrophy
Kim KP et al. Generation of a human iPSC line (MPIi007-A) from a patient with Metachromatic leukodystrophy. . 2020-10-00. Pubmed ID: 32950023; DOI: 10.1016/j.scr.2020.101993 MPIi007-A 2020-10-00 2020-10-00 PubMed: 32950023 DOI: 10.1016/j.scr.2020.101993Associated cell lines:
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Nur Patria Y, Stenta T, Lilianty J, Rowley L, Stanley EG, Elefanty AG, Bateman JF, Lamandé SR
CRISPR/Cas9 gene editing of a SOX9 reporter human iPSC line to produce two TRPV4 patient heterozygous missense mutant iPSC lines, MCRIi001-A-3 (TRPV4 p.F273L) and MCRIi001-A-4 (TRPV4 p.P799L)
Nur Patria Y et al. CRISPR/Cas9 gene editing of a SOX9 reporter human iPSC line to produce two TRPV4 patient heterozygous missense mutant iPSC lines, MCRIi001-A-3 (TRPV4 p.F273L) and MCRIi001-A-4 (TRPV4 p.P799L). . 2020-10-00. Pubmed ID: 32771907; DOI: 10.1016/j.scr.2020.101942 MCRIi001-AMCRIi001-A-2MCRIi001-A-3MCRIi001-A-4 2020-10-00 2020-10-00 PubMed: 32771907 DOI: 10.1016/j.scr.2020.101942Associated cell lines:
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Valetdinova KR, Maretina MA, Vyatkin YV, Perepelkina MP, Egorova AA, Baranov VS, Kiselev AV, Gershovich PM, Zakian SM
Generation of three Duchenne muscular dystrophy patient-derived induced pluripotent stem cell (iPSC) lines ICGi002-A, ICGi002-B and ICGi002-C
Valetdinova KR et al. Generation of three Duchenne muscular dystrophy patient-derived induced pluripotent stem cell (iPSC) lines ICGi002-A, ICGi002-B and ICGi002-C. . 2020-10-00. Pubmed ID: 32777771; DOI: 10.1016/j.scr.2020.101941 ICGi002-AICGi002-BICGi002-C 2020-10-00 2020-10-00 PubMed: 32777771 DOI: 10.1016/j.scr.2020.101941 -
Barbuti PA, Santos BFR, Dording CM, Cruciani G, Massart F, Hummel A, Krüger R
Generation of two iPS cell lines (HIHDNDi001-A and HIHDNDi001-B) from a Parkinson's disease patient carrying the heterozygous p.A30P mutation in SNCA
Barbuti PA et al. Generation of two iPS cell lines (HIHDNDi001-A and HIHDNDi001-B) from a Parkinson's disease patient carrying the heterozygous p.A30P mutation in SNCA. . 2020-10-00. Pubmed ID: 32798915; DOI: 10.1016/j.scr.2020.101951 LCSBi001-AHIHDNDi001-AHIHDNDi001-B 2020-10-00 2020-10-00 PubMed: 32798915 DOI: 10.1016/j.scr.2020.101951Associated cell lines:
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Wang W, Lv YF, Zhang YJ, Dong WJ, Zhang Y
Generation of a human induced pluripotent stem cell line PUMCi001-A from a patient with Krabbe disease
Wang W et al. Generation of a human induced pluripotent stem cell line PUMCi001-A from a patient with Krabbe disease. . 2020-10-00. Pubmed ID: 32763824; DOI: 10.1016/j.scr.2020.101937 PUMCi001-A 2020-10-00 2020-10-00 PubMed: 32763824 DOI: 10.1016/j.scr.2020.101937Associated cell lines:
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Ababneh NA, Al-Kurdi B, Ali D, Abuarqoub D, Barham R, Alzibdeh AM, Khanfar AN, Altantawi AM, Ryalat AT, Sharrack B, Awidi A
Generation and characterization of induced pluripotent stem cell (iPSC) line (JUCTCi002-A) from a patient with ataxia with oculomotor apraxia type 1 (AOA1) harboring a homozygous mutation in the APTX gene
Ababneh NA et al. Generation and characterization of induced pluripotent stem cell (iPSC) line (JUCTCi002-A) from a patient with ataxia with oculomotor apraxia type 1 (AOA1) harboring a homozygous mutation in the APTX gene. . 2020-10-00. Pubmed ID: 32769066; DOI: 10.1016/j.scr.2020.101925 JUCTCi002-A 2020-10-00 2020-10-00 PubMed: 32769066 DOI: 10.1016/j.scr.2020.101925Associated cell lines:
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Sripathy SR, Wang Y, Moses RL, Fatemi A, Batista DA, Maher BJ
Generation of 10 patient-specific induced pluripotent stem cells (iPSCs) to model Pitt-Hopkins Syndrome
Sripathy SR et al. Generation of 10 patient-specific induced pluripotent stem cells (iPSCs) to model Pitt-Hopkins Syndrome. . 2020-10-00. Pubmed ID: 32971458; DOI: 10.1016/j.scr.2020.102001; PMC: PMC7592084 LIBDi010-ALIBDi011-ALIBDi012-ALIBDi013-ALIBDi014-ALIBDi015-ALIBDi016-ALIBDi017-ALIBDi018-ALIBDi019-A 2020-10-00 2020-10-00 PubMed: 32971458 DOI: 10.1016/j.scr.2020.102001Associated cell lines:
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Dai Q, Zhang W, Guo J, Di W, Zhao J, Zhang B, Wang Y
Generation of an induced pluripotent stem cell line (SIAISi003-A) from a 79-year-old patient with Alzheimer's disease having APOE3/4 genetic background
Dai Q et al. Generation of an induced pluripotent stem cell line (SIAISi003-A) from a 79-year-old patient with Alzheimer's disease having APOE3/4 genetic background. . 2020-10-00. Pubmed ID: 32822964; DOI: 10.1016/j.scr.2020.101949 SIAISi003-A 2020-10-00 2020-10-00 PubMed: 32822964 DOI: 10.1016/j.scr.2020.101949Associated cell lines:
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Rajpurohit CS, Kumar V, Cheffer A, Oliveira D, Ulrich H, Okamoto OK, Zatz M, Ansari UA, Khanna VK, Pant AB
Mechanistic Insights of Astrocyte-Mediated Hyperactive Autophagy and Loss of Motor Neuron Function in SOD1(L39R) Linked Amyotrophic Lateral Sclerosis
Rajpurohit CS et al. Mechanistic Insights of Astrocyte-Mediated Hyperactive Autophagy and Loss of Motor Neuron Function in SOD1(L39R) Linked Amyotrophic Lateral Sclerosis. . 2020-10-00. Pubmed ID: 32676988; DOI: 10.1007/s12035-020-02006-0 HEBHMUi001-A 2020-10-00 2020-10-00 PubMed: 32676988 DOI: 10.1007/s12035-020-02006-0Associated cell lines:
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Falik D, Rabinski T, Zlotnik D, Eshel R, Zorsky M, Garin-Shkolnik T, Ofir R, Adato A, Ashkenazi A, Vatine GD
Generation and characterization of iPSC lines (BGUi004-A, BGUi005-A) from two identical twins with polyalanine expansion in the paired-like homeobox 2B (PHOX2B) gene
Falik D et al. Generation and characterization of iPSC lines (BGUi004-A, BGUi005-A) from two identical twins with polyalanine expansion in the paired-like homeobox 2B (PHOX2B) gene. . 2020-10-00. Pubmed ID: 32822965; DOI: 10.1016/j.scr.2020.101955 BGUi004-ABGUi005-A 2020-10-00 2020-10-00 PubMed: 32822965 DOI: 10.1016/j.scr.2020.101955 -
Tan C, Dai L, Yang W, Li F, Wang L, Xiao Y, Wang X, Zhang Y, Wang Y, Zeng C, Xiang Z, Zhang X, Zhang W, Ran Q, Chen M, Li Z, Chen L
Generation of the human induced pluripotent stem cell line (SHAMUi001-A) carrying the heterozygous c.-128G>T mutation in the 5'-UTR of the ANKRD26 gene
Tan C et al. Generation of the human induced pluripotent stem cell line (SHAMUi001-A) carrying the heterozygous c.-128G>T mutation in the 5'-UTR of the ANKRD26 gene. . 2020-10-00. Pubmed ID: 32979630; DOI: 10.1016/j.scr.2020.102002 SHAMUi001-A 2020-10-00 2020-10-00 PubMed: 32979630 DOI: 10.1016/j.scr.2020.102002Associated cell lines:
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Peron C, Mauceri R, Cabassi T, Segnali A, Maresca A, Iannielli A, Rizzo A, Sciacca FL, Broccoli V, Carelli V, Tiranti V
Generation of a human iPSC line, FINCBi001-A, carrying a homoplasmic m.G3460A mutation in MT-ND1 associated with Leber's Hereditary optic Neuropathy (LHON)
Peron C et al. Generation of a human iPSC line, FINCBi001-A, carrying a homoplasmic m.G3460A mutation in MT-ND1 associated with Leber's Hereditary optic Neuropathy (LHON). . 2020-10-00. Pubmed ID: 32771908; DOI: 10.1016/j.scr.2020.101939 FINCBi001-A 2020-10-00 2020-10-00 PubMed: 32771908 DOI: 10.1016/j.scr.2020.101939Associated cell lines:
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Zhou XB, Li H, Li F, Song XK, Liu T, Ma T, Guo HY, Wu N, Li J
Generation and characterization of two iPSC lines from human adipose tissue-derived stem cells of healthy donors
Zhou XB et al. Generation and characterization of two iPSC lines from human adipose tissue-derived stem cells of healthy donors. . 2020-10-00. Pubmed ID: 32896746; DOI: 10.1016/j.scr.2020.101973 BIPTi001-ABIPTi002-A 2020-10-00 2020-10-00 PubMed: 32896746 DOI: 10.1016/j.scr.2020.101973Associated cell lines:
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Wu X, Zhao Y, Wang X
Generation of a human embryonic stem cell line (WAe009-A-43) carrying a Long QT syndrome related mutation in KCNH2 gene
Wu X et al. Generation of a human embryonic stem cell line (WAe009-A-43) carrying a Long QT syndrome related mutation in KCNH2 gene. . 2020-10-00. Pubmed ID: 32911324; DOI: 10.1016/j.scr.2020.101976 WAe009-AWAe009-A-43 2020-10-00 2020-10-00 PubMed: 32911324 DOI: 10.1016/j.scr.2020.101976Associated cell lines:
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Jennings L, Zhang D, Chen SC, Moon SY, Lamey T, Thompson JA, McLaren T, De Roach JN, Chen FK, McLenachan S
Generation of two induced pluripotent stem cell lines from a patient with Stargardt Macular Dystrophy caused by the c.768G>T and c.6079C>T mutations in ABCA4
Jennings L et al. Generation of two induced pluripotent stem cell lines from a patient with Stargardt Macular Dystrophy caused by the c.768G>T and c.6079C>T mutations in ABCA4. . 2020-10-00. Pubmed ID: 32810830; DOI: 10.1016/j.scr.2020.101947 LEIi012-ALEIi012-B 2020-10-00 2020-10-00 PubMed: 32810830 DOI: 10.1016/j.scr.2020.101947 -
Kung LHW, Sampurno L, Yammine KM, Graham A, McDonald P, Bateman JF, Shoulders MD, Lamandé SR
CRISPR/Cas9 editing to generate a heterozygous COL2A1 p.G1170S human chondrodysplasia iPSC line, MCRIi019-A-2, in a control iPSC line, MCRIi019-A
Kung LHW et al. CRISPR/Cas9 editing to generate a heterozygous COL2A1 p.G1170S human chondrodysplasia iPSC line, MCRIi019-A-2, in a control iPSC line, MCRIi019-A. . 2020-10-00. Pubmed ID: 33002832; DOI: 10.1016/j.scr.2020.101962 MCRIi019-AMCRIi019-A-2 2020-10-00 2020-10-00 PubMed: 33002832 DOI: 10.1016/j.scr.2020.101962Associated cell lines:
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Zhao H, He L, Huang H, Li S, Cheng N, Tang F, Han X, Lin Z, Huang R, Zhou P, Deng S, Huang J, Li Z
Generation of a tdTomato-GAD67 reporter human epilepsia mutation induced pluripotent stem cell line, USTCi001-A-2, using CRISPR/Cas9 editing
Zhao H et al. Generation of a tdTomato-GAD67 reporter human epilepsia mutation induced pluripotent stem cell line, USTCi001-A-2, using CRISPR/Cas9 editing. . 2020-10-00. Pubmed ID: 32977294; DOI: 10.1016/j.scr.2020.102003 USTCi001-AUSTCi001-A-2 2020-10-00 2020-10-00 PubMed: 32977294 DOI: 10.1016/j.scr.2020.102003Associated cell lines:
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Lorthongpanich C, Laowtammathron C, Jiamvoraphong N, Srisook P, Chingsuwanrote P, Klaihmon P, Waeteekul S, U-Pratya Y, Issaragrisil S
Generation of a serine/threonine-protein kinase LATS1 gene-edited iPSC MUSIi012-A-3
Lorthongpanich C et al. Generation of a serine/threonine-protein kinase LATS1 gene-edited iPSC MUSIi012-A-3. . 2020-10-00. Pubmed ID: 32791482; DOI: 10.1016/j.scr.2020.101950 MUSIi012-AMUSIi012-A-3 2020-10-00 2020-10-00 PubMed: 32791482 DOI: 10.1016/j.scr.2020.101950Associated cell lines:
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Sahabian A, von Schlehdorn L, Drick N, Pink I, Dahlmann J, Haase A, Göhring G, Welte T, Martin U, Ringshausen FC, Olmer R
Generation of two hiPSC clones (MHHi019-A, MHHi019-B) from a primary ciliary dyskinesia patient carrying a homozygous deletion in the NME5 gene (c.415delA (p.Ile139Tyrfs*8))
Sahabian A et al. Generation of two hiPSC clones (MHHi019-A, MHHi019-B) from a primary ciliary dyskinesia patient carrying a homozygous deletion in the NME5 gene (c.415delA (p.Ile139Tyrfs*8)). . 2020-10-00. Pubmed ID: 32950024; DOI: 10.1016/j.scr.2020.101988 MHHi019-AMHHi019-B 2020-10-00 2020-10-00 PubMed: 32950024 DOI: 10.1016/j.scr.2020.101988 -
Wu F, Li X, Bai R, Li Y, Gao J, Lan F
Generation of a Junctophilin-2 homozygous knockout human embryonic stem cell line (WAe009-A-36) by an episomal vector-based CRISPR/Cas9 system
Wu F et al. Generation of a Junctophilin-2 homozygous knockout human embryonic stem cell line (WAe009-A-36) by an episomal vector-based CRISPR/Cas9 system. . 2020-10-00. Pubmed ID: 32777767; DOI: 10.1016/j.scr.2020.101930 WAe009-AWAe009-A-36WAe009-A-1EWAe009-A-1H 2020-10-00 2020-10-00 PubMed: 32777767 DOI: 10.1016/j.scr.2020.101930Associated cell lines:
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Sung JJ, Park S, Choi SH, Kim J, Cho MS, Kim DW
Generation of a gene edited hemophilia A patient-derived iPSC cell line, YCMi001-B-1, by targeted insertion of coagulation factor FVIII using CRISPR/Cas9
Sung JJ et al. Generation of a gene edited hemophilia A patient-derived iPSC cell line, YCMi001-B-1, by targeted insertion of coagulation factor FVIII using CRISPR/Cas9. . 2020-10-00. Pubmed ID: 32798916; DOI: 10.1016/j.scr.2020.101948 YCMi001-BYCMi001-B-1 2020-10-00 2020-10-00 PubMed: 32798916 DOI: 10.1016/j.scr.2020.101948Associated cell lines:
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Yang J, Liu H, Sun H, Wang Z, Zhang R, Liu Y, Zhang Q, Zhang S, Zhang J, Shi C, Wang Y, Xu Y
Construction of induced pluripotent stem cell line (ZZUi0017-A) from the fibroblast cells of a female patient with CACNA1A mutation by unintegrated reprogramming approach
Yang J et al. Construction of induced pluripotent stem cell line (ZZUi0017-A) from the fibroblast cells of a female patient with CACNA1A mutation by unintegrated reprogramming approach. . 2020-10-00. Pubmed ID: 32791484; DOI: 10.1016/j.scr.2020.101946 ZZUi017-A 2020-10-00 2020-10-00 PubMed: 32791484 DOI: 10.1016/j.scr.2020.101946Associated cell lines:
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Stock R, Vogel S, Mau-Holzmann UA, Kriebel M, Wüst R, Fallgatter AJ, Volkmer H
Generation and characterization of human induced pluripotent stem cells lines from four patients diagnosed with schizophrenia and one healthy control
Stock R et al. Generation and characterization of human induced pluripotent stem cells lines from four patients diagnosed with schizophrenia and one healthy control. . 2020-10-00. Pubmed ID: 32911325; DOI: 10.1016/j.scr.2020.101961 NMIi001-ANMIi002-ANMIi004-ANMIi005-ANMIi006-ANMIi002-BNMIi006-B 2020-10-00 2020-10-00 PubMed: 32911325 DOI: 10.1016/j.scr.2020.101961 -
Ovechkina VS, Maretina MA, Egorova AA, Baranov VS, Kiselev AV, Zakian SM, Valetdinova KR
Generation of a spinal muscular atrophy type III patient-specific induced pluripotent stem cell line ICGi003-A
Ovechkina VS et al. Generation of a spinal muscular atrophy type III patient-specific induced pluripotent stem cell line ICGi003-A. . 2020-10-00. Pubmed ID: 32795928; DOI: 10.1016/j.scr.2020.101938 ICGi003-A 2020-10-00 2020-10-00 PubMed: 32795928 DOI: 10.1016/j.scr.2020.101938Associated cell lines:
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Schmid B, Prehn KR, Nimsanor N, Garcia BIA, Poulsen U, Jørring I, Rasmussen MA, Clausen C, Mau-Holzmann UA, Ramakrishna S, Muddashetty R, Steeg R, Bruce K, Mackintosh P, Ebneth A, Holst B, Cabrera-Socorro A
Corrigendum to "Generation of a set of isogenic, gene-edited iPSC lines homozygous for all main APOE variants and an APOE knock-out line" [Stem Cell Res. 34/1873-5061 (2019) 101349-55]
Schmid B et al. Corrigendum to "Generation of a set of isogenic, gene-edited iPSC lines homozygous for all main APOE variants and an APOE knock-out line" [Stem Cell Res. 34/1873-5061 (2019) 101349-55]. . 2020-10-00. Pubmed ID: 32971461; DOI: 10.1016/j.scr.2020.102005 BIONi010-CBIONi010-C-2BIONi010-C-3BIONi010-C-4BIONi010-C-6 2020-10-00 2020-10-00 PubMed: 32971461 DOI: 10.1016/j.scr.2020.102005Associated cell lines:
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Lee SJ, Kim JH, Kang KW, Park Y, Kim BS
Supporting data on enhanced reprogramming of human CD34+ hematopoietic stem cells to induced pluripotent stem cells using human placenta-derived cell conditioned medium
Lee SJ et al. Supporting data on enhanced reprogramming of human CD34+ hematopoietic stem cells to induced pluripotent stem cells using human placenta-derived cell conditioned medium. . 2020-10-00. Pubmed ID: 32904343; DOI: 10.1016/j.dib.2020.106140; PMC: PMC7452686 KUMCi001-A 2020-10-00 2020-10-00 PubMed: 32904343 DOI: 10.1016/j.dib.2020.106140Associated cell lines:
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Das D, Li J, Liu S, Oh E, Cheng L, Lyketsos C, Mahairaki V
Generation and characterization of a novel human iPSC line from a resilient Alzheimer's disease patient
Das D et al. Generation and characterization of a novel human iPSC line from a resilient Alzheimer's disease patient. . 2020-10-00. Pubmed ID: 32916633; DOI: 10.1016/j.scr.2020.101979 JHUi002-A 2020-10-00 2020-10-00 PubMed: 32916633 DOI: 10.1016/j.scr.2020.101979Associated cell lines:
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Zhang Y, Wu Z, Li X, Wan Y, Zhang Y, Zhao P
Maternal sevoflurane exposure affects differentiation of hippocampal neural stem cells by regulating miR-410-3p and ATN1
Zhang Y et al. Maternal sevoflurane exposure affects differentiation of hippocampal neural stem cells by regulating miR-410-3p and ATN1. . 2020-09-29. Pubmed ID: 32993796; DOI: 10.1186/s13287-020-01936-9; PMC: PMC7523391 CSSi008-A 2020-09-29 2020-09-29 PubMed: 32993796 DOI: 10.1186/s13287-020-01936-9Associated cell lines:
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Vagiona AC, Andrade-Navarro MA, Psomopoulos F, Petrakis S
Dynamics of a Protein Interaction Network Associated to the Aggregation of polyQ-Expanded Ataxin-1
Vagiona AC et al. Dynamics of a Protein Interaction Network Associated to the Aggregation of polyQ-Expanded Ataxin-1. . 2020-09-25. Pubmed ID: 32992839; DOI: 10.3390/genes11101129; PMC: PMC7600199 LUMCi002-ALUMCi003-A 2020-09-25 2020-09-25 PubMed: 32992839 DOI: 10.3390/genes11101129Associated cell lines:
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Rovina D, Castiglioni E, Niro F, Mallia S, Pompilio G, Gowran A
"Betwixt Mine Eye and Heart a League Is Took": The Progress of Induced Pluripotent Stem-Cell-Based Models of Dystrophin-Associated Cardiomyopathy
Rovina D et al. "Betwixt Mine Eye and Heart a League Is Took": The Progress of Induced Pluripotent Stem-Cell-Based Models of Dystrophin-Associated Cardiomyopathy. . 2020-09-23. Pubmed ID: 32977524; DOI: 10.3390/ijms21196997; PMC: PMC7582534 MUNIi001-AMUNIi003-AIITi001-ACCMi003-ASDQLCHi007-A 2020-09-23 2020-09-23 PubMed: 32977524 DOI: 10.3390/ijms21196997Associated cell lines:
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Coyne AN, Zaepfel BL, Hayes L, Fitchman B, Salzberg Y, Luo EC, Bowen K, Trost H, Aigner S, Rigo F, Yeo GW, Harel A, Svendsen CN, Sareen D, Rothstein JD
G(4)C(2) Repeat RNA Initiates a POM121-Mediated Reduction in Specific Nucleoporins in C9orf72 ALS/FTD
Coyne AN et al. G(4)C(2) Repeat RNA Initiates a POM121-Mediated Reduction in Specific Nucleoporins in C9orf72 ALS/FTD. . 2020-09-23. Pubmed ID: 32673563; DOI: 10.1016/j.neuron.2020.06.027; PMC: PMC8077944 EDi022-AEDi029-AEDi034-AEDi036-AEDi037-AEDi043-AEDi044-A 2020-09-23 2020-09-23 PubMed: 32673563 DOI: 10.1016/j.neuron.2020.06.027 -
Cowan CS, Renner M, De Gennaro M, Gross-Scherf B, Goldblum D, Hou Y, Munz M, Rodrigues TM, Krol J, Szikra T, Cuttat R, Waldt A, Papasaikas P, Diggelmann R, Patino-Alvarez CP, Galliker P, Spirig SE, Pavlinic D, Gerber-Hollbach N, Schuierer S, Srdanovic A, Balogh M, Panero R, Kusnyerik A, Szabo A, Stadler MB, Orgül S, Picelli S, Hasler PW, Hierlemann A, Scholl HPN, Roma G, Nigsch F, Roska B
Cell Types of the Human Retina and Its Organoids at Single-Cell Resolution
Cowan CS et al. Cell Types of the Human Retina and Its Organoids at Single-Cell Resolution. . 2020-09-17. Pubmed ID: 32946783; DOI: 10.1016/j.cell.2020.08.013; PMC: PMC7505495 WISCi004-BIOBi001-A 2020-09-17 2020-09-17 PubMed: 32946783 DOI: 10.1016/j.cell.2020.08.013Associated cell lines:
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Tang Y, Han Y, Yu H, Zhang B, Li G
Increased GABAergic development in iPSC-derived neurons from patients with sporadic Alzheimer's disease
Tang Y et al. Increased GABAergic development in iPSC-derived neurons from patients with sporadic Alzheimer's disease. . 2020-09-14. Pubmed ID: 32615251; DOI: 10.1016/j.neulet.2020.135208 TUSMi001-ATUSMi008-A 2020-09-14 2020-09-14 PubMed: 32615251 DOI: 10.1016/j.neulet.2020.135208Associated cell lines:
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Yu Z, Dmitrieva NI, Walts AD, Jin H, Liu Y, Ping X, Ferrante EA, Qiu L, Holland SM, Freeman AF, Chen G, Boehm M
STAT3 modulates reprogramming efficiency of human somatic cells; insights from autosomal dominant Hyper IgE syndrome caused by STAT3 mutations
Yu Z et al. STAT3 modulates reprogramming efficiency of human somatic cells; insights from autosomal dominant Hyper IgE syndrome caused by STAT3 mutations. . 2020-09-10. Pubmed ID: 32580970; DOI: 10.1242/bio.052662; PMC: PMC7502598 NIHTVBi011-ANIHTVBi012-ANIHTVBi013-A 2020-09-10 2020-09-10 PubMed: 32580970 DOI: 10.1242/bio.052662Associated cell lines:
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Barbuti P, Antony P, Santos B, Massart F, Cruciani G, Dording C, Arias J, Schwamborn J, Krüger R
Using High-Content Screening to Generate Single-Cell Gene-Corrected Patient-Derived iPS Clones Reveals Excess Alpha-Synuclein with Familial Parkinson's Disease Point Mutation A30P
Barbuti P et al. Using High-Content Screening to Generate Single-Cell Gene-Corrected Patient-Derived iPS Clones Reveals Excess Alpha-Synuclein with Familial Parkinson's Disease Point Mutation A30P. . 2020-09-10. Pubmed ID: 32927687; DOI: 10.3390/cells9092065; PMC: PMC7564375 HIHDNDi001-AHIHDNDi001-B 2020-09-10 2020-09-10 PubMed: 32927687 DOI: 10.3390/cells9092065Associated cell lines:
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Briganti F, Sun H, Wei W, Wu J, Zhu C, Liss M, Karakikes I, Rego S, Cipriano A, Snyder M, Meder B, Xu Z, Millat G, Gotthardt M, Mercola M, Steinmetz LM
iPSC Modeling of RBM20-Deficient DCM Identifies Upregulation of RBM20 as a Therapeutic Strategy
Briganti F et al. iPSC Modeling of RBM20-Deficient DCM Identifies Upregulation of RBM20 as a Therapeutic Strategy. . 2020-09-08. Pubmed ID: 32905764; DOI: 10.1016/j.celrep.2020.108117; PMC: PMC8168789 UCSFi001-A-64UCSFi001-A-65 2020-09-08 2020-09-08 PubMed: 32905764 DOI: 10.1016/j.celrep.2020.108117Associated cell lines:
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Ferreira Mendes JM, de Faro Valverde L, Torres Andion Vidal M, Paredes BD, Coelho P, Allahdadi KJ, Coletta RD, Souza BSF, Rocha CAG
Effects of IGF-1 on Proliferation, Angiogenesis, Tumor Stem Cell Populations and Activation of AKT and Hedgehog Pathways in Oral Squamous Cell Carcinoma
Ferreira Mendes JM et al. Effects of IGF-1 on Proliferation, Angiogenesis, Tumor Stem Cell Populations and Activation of AKT and Hedgehog Pathways in Oral Squamous Cell Carcinoma. . 2020-09-05. Pubmed ID: 32899449; DOI: 10.3390/ijms21186487; PMC: PMC7555130 CBTCi001-A 2020-09-05 2020-09-05 PubMed: 32899449 DOI: 10.3390/ijms21186487Associated cell lines:
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Novak Gabriela, Kyriakis Dimitrios, Grzyb Kamil, Bernini Michela, Finkbeiner Steven, Skupin Alexander
Single cell transcriptomics of human PINK1 iPSC differentiation dynamics reveal a core network of Parkinson’s disease
Novak Gabriela et al. Single cell transcriptomics of human PINK1 iPSC differentiation dynamics reveal a core network of Parkinson’s disease. . 2020-09-05. DOI: 10.21203/rs.3.rs-72882/v1 LCSBi002-BLCSBi004-ALCSBi004-B 2020-09-05 2020-09-05 DOI: 10.21203/rs.3.rs-72882/v1Associated cell lines:
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Huang W.
The challenges and views in precise diagnosis and treatment of Alport syndrome
Huang W.. The challenges and views in precise diagnosis and treatment of Alport syndrome. . 2020-09-05. DOI: 10.3760/cma.j.cn101070-20200729-01264 SHCDNRi001-A 2020-09-05 2020-09-05 DOI: 10.3760/cma.j.cn101070-20200729-01264Associated cell lines:
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Khoa LTP, Tsan YC, Mao F, Kremer DM, Sajjakulnukit P, Zhang L, Zhou B, Tong X, Bhanu NV, Choudhary C, Garcia BA, Yin L, Smith GD, Saunders TL, Bielas SL, Lyssiotis CA, Dou Y
Histone Acetyltransferase MOF Blocks Acquisition of Quiescence in Ground-State ESCs through Activating Fatty Acid Oxidation
Khoa LTP et al. Histone Acetyltransferase MOF Blocks Acquisition of Quiescence in Ground-State ESCs through Activating Fatty Acid Oxidation. . 2020-09-03. Pubmed ID: 32610040; DOI: 10.1016/j.stem.2020.06.005; PMC: PMC7758074 WAe009-A 2020-09-03 2020-09-03 PubMed: 32610040 DOI: 10.1016/j.stem.2020.06.005Associated cell lines:
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Muñoz SS, Engel M, Balez R, Do-Ha D, Cabral-da-Silva MC, Hernández D, Berg T, Fifita JA, Grima N, Yang S, Blair IP, Nicholson G, Cook AL, Hewitt AW, Pébay A, Ooi L
A Simple Differentiation Protocol for Generation of Induced Pluripotent Stem Cell-Derived Basal Forebrain-Like Cholinergic Neurons for Alzheimer's Disease and Frontotemporal Dementia Disease Modeling
Muñoz SS et al. A Simple Differentiation Protocol for Generation of Induced Pluripotent Stem Cell-Derived Basal Forebrain-Like Cholinergic Neurons for Alzheimer's Disease and Frontotemporal Dementia Disease Modeling. . 2020-09-02. Pubmed ID: 32887382; DOI: 10.3390/cells9092018; PMC: PMC7564334 UOWi001-AUOWi002-AUOWi003-AUOWi006-AUOWi008-A 2020-09-02 2020-09-02 PubMed: 32887382 DOI: 10.3390/cells9092018 -
Genova E, Stocco G, Decorti G
Induced pluripotent stem cells to model adverse drug reactions in pediatric patients
Genova E et al. Induced pluripotent stem cells to model adverse drug reactions in pediatric patients. . 2020-09-00. Pubmed ID: 32893744; DOI: 10.2217/pgs-2020-0082 UNIBSi008-AUNIBSi008-BUNIBSi008-C 2020-09-00 2020-09-00 PubMed: 32893744 DOI: 10.2217/pgs-2020-0082Associated cell lines:
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Meynier S, Rieux-Laucat F
After 95 years, it's time to eRASe JMML
Meynier S et al. After 95 years, it's time to eRASe JMML. . 2020-09-00. Pubmed ID: 31980238; DOI: 10.1016/j.blre.2020.100652 CHOPi001-A 2020-09-00 2020-09-00 PubMed: 31980238 DOI: 10.1016/j.blre.2020.100652Associated cell lines:
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Porta F, Ponzone A, Spada M
Phenylalanine and tyrosine metabolism in DNAJC12 deficiency: A comparison between inherited hyperphenylalaninemias and healthy subjects
Porta F et al. Phenylalanine and tyrosine metabolism in DNAJC12 deficiency: A comparison between inherited hyperphenylalaninemias and healthy subjects. . 2020-09-00. Pubmed ID: 32800687; DOI: 10.1016/j.ejpn.2020.07.011 DHMCi003-ADHMCi003-B 2020-09-00 2020-09-00 PubMed: 32800687 DOI: 10.1016/j.ejpn.2020.07.011Associated cell lines:
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Calzari L, Barcella M, Alari V, Braga D, Muñoz-Viana R, Barlassina C, Finelli P, Gervasini C, Barco A, Russo S, Larizza L
Transcriptome Analysis of iPSC-Derived Neurons from Rubinstein-Taybi Patients Reveals Deficits in Neuronal Differentiation
Calzari L et al. Transcriptome Analysis of iPSC-Derived Neurons from Rubinstein-Taybi Patients Reveals Deficits in Neuronal Differentiation. . 2020-09-00. Pubmed ID: 32562237; DOI: 10.1007/s12035-020-01983-6; PMC: PMC7399686 IAIi001-AIAIi002-AIAIi003-AIAIi004-A 2020-09-00 2020-09-00 PubMed: 32562237 DOI: 10.1007/s12035-020-01983-6 -
Shrestha R, Wen YT, Tsai RK
Effective Differentiation and Biological Characterization of Retinal Pigment Epithelium Derived from Human Induced Pluripotent Stem Cells
Shrestha R et al. Effective Differentiation and Biological Characterization of Retinal Pigment Epithelium Derived from Human Induced Pluripotent Stem Cells. . 2020-09-00. Pubmed ID: 31984806; DOI: 10.1080/02713683.2020.1722180 TCIERi001-A 2020-09-00 2020-09-00 PubMed: 31984806 DOI: 10.1080/02713683.2020.1722180Associated cell lines:
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Egorova P. A., Bezprozvanny I. B.
New Approaches in Studies of the Molecular Pathogenesis of Type 2 Spinocerebellar Ataxia
Egorova P. A. et al. New Approaches in Studies of the Molecular Pathogenesis of Type 2 Spinocerebellar Ataxia. . 2020-09-00. DOI: 10.1007/s11055-020-00988-x CHOPi002-ACHOPi003-A 2020-09-00 2020-09-00 DOI: 10.1007/s11055-020-00988-xAssociated cell lines:
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56(th) EASD Annual Meeting of the European Association for the Study of Diabetes : 21-25 September 2020
(unknown author). 56(th) EASD Annual Meeting of the European Association for the Study of Diabetes : 21-25 September 2020. . 2020-09-00. Pubmed ID: 32840677; DOI: 10.1007/s00125-020-05221-5; PMC: PMC7445463 MHHi006-A 2020-09-00 2020-09-00 PubMed: 32840677 DOI: 10.1007/s00125-020-05221-5Associated cell lines:
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Marchiano Silvia, Hsiang Tien-Ying, Higashi Ty, Khanna Akshita, Reinecke Hans, Yang Xiulan, Pabon Lil, Sniadecki Nathan J., Bertero Alessandro, Gale Michael, Murry Charles E.
SARS-CoV-2 infects human pluripotent stem cell-derived cardiomyocytes, impairing electrical and mechanical function
Marchiano Silvia et al. SARS-CoV-2 infects human pluripotent stem cell-derived cardiomyocytes, impairing electrical and mechanical function. . 2020-08-30. DOI: 10.1101/2020.08.30.274464 RUESe002-A 2020-08-30 2020-08-30 DOI: 10.1101/2020.08.30.274464Associated cell lines:
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Ebrahimi V, Hashemi A
Challenges of in vitro genome editing with CRISPR/Cas9 and possible solutions: A review
Ebrahimi V et al. Challenges of in vitro genome editing with CRISPR/Cas9 and possible solutions: A review. . 2020-08-30. Pubmed ID: 32470504; DOI: 10.1016/j.gene.2020.144813 MUSIi012-AMUSIi012-A-1 2020-08-30 2020-08-30 PubMed: 32470504 DOI: 10.1016/j.gene.2020.144813Associated cell lines:
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Han L, Chaturvedi P, Kishimoto K, Koike H, Nasr T, Iwasawa K, Giesbrecht K, Witcher PC, Eicher A, Haines L, Lee Y, Shannon JM, Morimoto M, Wells JM, Takebe T, Zorn AM
Single cell transcriptomics identifies a signaling network coordinating endoderm and mesoderm diversification during foregut organogenesis
Han L et al. Single cell transcriptomics identifies a signaling network coordinating endoderm and mesoderm diversification during foregut organogenesis. . 2020-08-27. Pubmed ID: 32855417; DOI: 10.1038/s41467-020-17968-x; PMC: PMC7453027 CUSTOMi001-A 2020-08-27 2020-08-27 PubMed: 32855417 DOI: 10.1038/s41467-020-17968-xAssociated cell lines:
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Sanjurjo-Rodríguez C, Castro-Viñuelas R, Piñeiro-Ramil M, Rodríguez-Fernández S, Fuentes-Boquete I, Blanco FJ, Díaz-Prado S
Versatility of Induced Pluripotent Stem Cells (iPSCs) for Improving the Knowledge on Musculoskeletal Diseases
Sanjurjo-Rodríguez C et al. Versatility of Induced Pluripotent Stem Cells (iPSCs) for Improving the Knowledge on Musculoskeletal Diseases. . 2020-08-25. Pubmed ID: 32854405; DOI: 10.3390/ijms21176124; PMC: PMC7504376 ISMMSi002-BUCLi011-AUCLi012-AMCRIi018-AMCRIi018-BESi080-A 2020-08-25 2020-08-25 PubMed: 32854405 DOI: 10.3390/ijms21176124Associated cell lines:
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Kumamoto T, Maurinot F, Barry-Martinet R, Vaslin C, Vandormael-Pournin S, Le M, Lerat M, Niculescu D, Cohen-Tannoudji M, Rebsam A, Loulier K, Nedelec S, Tozer S, Livet J
Direct Readout of Neural Stem Cell Transgenesis with an Integration-Coupled Gene Expression Switch
Kumamoto T et al. Direct Readout of Neural Stem Cell Transgenesis with an Integration-Coupled Gene Expression Switch. . 2020-08-19. Pubmed ID: 32559415; DOI: 10.1016/j.neuron.2020.05.038; PMC: PMC7447981 WTSIi008-A 2020-08-19 2020-08-19 PubMed: 32559415 DOI: 10.1016/j.neuron.2020.05.038Associated cell lines:
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Kaewkhaw R, Rojanaporn D
Retinoblastoma: Etiology, Modeling, and Treatment
Kaewkhaw R et al. Retinoblastoma: Etiology, Modeling, and Treatment. . 2020-08-16. Pubmed ID: 32824373; DOI: 10.3390/cancers12082304; PMC: PMC7465685 VRFi001-A 2020-08-16 2020-08-16 PubMed: 32824373 DOI: 10.3390/cancers12082304Associated cell lines:
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Amano G, Matsuzaki S, Mori Y, Miyoshi K, Han S, Shikada S, Takamura H, Yoshimura T, Katayama T
SCYL1 arginine methylation by PRMT1 is essential for neurite outgrowth via Golgi morphogenesis
Amano G et al. SCYL1 arginine methylation by PRMT1 is essential for neurite outgrowth via Golgi morphogenesis. . 2020-08-15. Pubmed ID: 32583741; DOI: 10.1091/mbc.e20-02-0100; PMC: PMC7543066 DHMCi005-A 2020-08-15 2020-08-15 PubMed: 32583741 DOI: 10.1091/mbc.e20-02-0100Associated cell lines:
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Wang L, Li Z, Sievert D, Smith DEC, Mendes MI, Chen DY, Stanley V, Ghosh S, Wang Y, Kara M, Aslanger AD, Rosti RO, Houlden H, Salomons GS, Gleeson JG
Loss of NARS1 impairs progenitor proliferation in cortical brain organoids and leads to microcephaly
Wang L et al. Loss of NARS1 impairs progenitor proliferation in cortical brain organoids and leads to microcephaly. . 2020-08-12. Pubmed ID: 32788587; DOI: 10.1038/s41467-020-17454-4; PMC: PMC7424529 WAe001-A 2020-08-12 2020-08-12 PubMed: 32788587 DOI: 10.1038/s41467-020-17454-4Associated cell lines:
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Riccetti S, Sinigaglia A, Desole G, Nowotny N, Trevisan M, Barzon L
Modelling West Nile Virus and Usutu Virus Pathogenicity in Human Neural Stem Cells
Riccetti S et al. Modelling West Nile Virus and Usutu Virus Pathogenicity in Human Neural Stem Cells. . 2020-08-12. Pubmed ID: 32806715; DOI: 10.3390/v12080882; PMC: PMC7471976 UNIPDi002-A 2020-08-12 2020-08-12 PubMed: 32806715 DOI: 10.3390/v12080882Associated cell lines:
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Kobold S, Guhr A, Mah N, Bultjer N, Seltmann S, Seiler Wulczyn AEM, Stacey G, Jie H, Liu W, Löser P, Kurtz A
A Manually Curated Database on Clinical Studies Involving Cell Products Derived from Human Pluripotent Stem Cells
Kobold S et al. A Manually Curated Database on Clinical Studies Involving Cell Products Derived from Human Pluripotent Stem Cells. . 2020-08-11. Pubmed ID: 32679065; DOI: 10.1016/j.stemcr.2020.06.014; PMC: PMC7419703 TECHe003-AAXORe001-AACTe002-AWAe001-AWAe009-ARCe013-AVCYTe001-AHADe007-AHADe008-A 2020-08-11 2020-08-11 PubMed: 32679065 DOI: 10.1016/j.stemcr.2020.06.014Associated cell lines:
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Evans Lewis D., Strano Alessio, Tuck Eleanor, Campbell Ashley, Smith James, Hung Christy, Behr Tiana S., Ghetti Bernardino, Ryskeldi-Falcon Benjamin, Karakoc Emre, Iorio Francesco, Reith Alastair, Bassett Andrew R., Livesey Frederick J.
Whole genome CRISPR screens identify a LRRK2-regulated pathway for extracellular tau uptake by human neurons
Evans Lewis D. et al. Whole genome CRISPR screens identify a LRRK2-regulated pathway for extracellular tau uptake by human neurons. . 2020-08-11. DOI: 10.1101/2020.08.11.246363 WTSIi018-BWTSIi018-B-1 2020-08-11 2020-08-11 DOI: 10.1101/2020.08.11.246363Associated cell lines:
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Nieuwenhuis B, Barber AC, Evans RS, Pearson CS, Fuchs J, MacQueen AR, van Erp S, Haenzi B, Hulshof LA, Osborne A, Conceicao R, Khatib TZ, Deshpande SS, Cave J, Ffrench-Constant C, Smith PD, Okkenhaug K, Eickholt BJ, Martin KR, Fawcett JW, Eva R
PI 3-kinase delta enhances axonal PIP(3) to support axon regeneration in the adult CNS
Nieuwenhuis B et al. PI 3-kinase delta enhances axonal PIP(3) to support axon regeneration in the adult CNS. . 2020-08-07. Pubmed ID: 32558386; DOI: 10.15252/emmm.201911674; PMC: PMC7411663 RCe015-ARCe021-A 2020-08-07 2020-08-07 PubMed: 32558386 DOI: 10.15252/emmm.201911674 -
Dmitrieva NI, Walts AD, Nguyen DP, Grubb A, Zhang X, Wang X, Ping X, Jin H, Yu Z, Yu ZX, Yang D, Schwartzbeck R, Dalgard CL, Kozel BA, Levin MD, Knutsen RH, Liu D, Milner JD, López DB, O'Connell MP, Lee CR, Myles IA, Hsu AP, Freeman AF, Holland SM, Chen G, Boehm M
Impaired angiogenesis and extracellular matrix metabolism in autosomal-dominant hyper-IgE syndrome
Dmitrieva NI et al. Impaired angiogenesis and extracellular matrix metabolism in autosomal-dominant hyper-IgE syndrome. . 2020-08-03. Pubmed ID: 32369445; DOI: 10.1172/jci135490; PMC: PMC7410079 NIHTVBi011-ANIHTVBi012-ANIHTVBi013-A 2020-08-03 2020-08-03 PubMed: 32369445 DOI: 10.1172/jci135490Associated cell lines:
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D'Adamo MC, Liantonio A, Conte E, Pessia M, Imbrici P
Ion Channels Involvement in Neurodevelopmental Disorders
D'Adamo MC et al. Ion Channels Involvement in Neurodevelopmental Disorders. . 2020-08-01. Pubmed ID: 32473276; DOI: 10.1016/j.neuroscience.2020.05.032 HIHDNEi002-A 2020-08-01 2020-08-01 PubMed: 32473276 DOI: 10.1016/j.neuroscience.2020.05.032Associated cell lines:
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Genova E, Cavion F, Lucafò M, Pelin M, Lanzi G, Masneri S, Ferraro RM, Fazzi EM, Orcesi S, Decorti G, Tommasini A, Giliani S, Stocco G
Biomarkers and Precision Therapy for Primary Immunodeficiencies: An In Vitro Study Based on Induced Pluripotent Stem Cells From Patients
Genova E et al. Biomarkers and Precision Therapy for Primary Immunodeficiencies: An In Vitro Study Based on Induced Pluripotent Stem Cells From Patients. . 2020-08-00. Pubmed ID: 32243572; DOI: 10.1002/cpt.1837 UNIBSi008-AUNIBSi008-BUNIBSi008-C 2020-08-00 2020-08-00 PubMed: 32243572 DOI: 10.1002/cpt.1837Associated cell lines:
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Petrus-Reurer S, Kumar P, Padrell Sánchez S, Aronsson M, André H, Bartuma H, Plaza Reyes A, Nandrot EF, Kvanta A, Lanner F
Preclinical safety studies of human embryonic stem cell-derived retinal pigment epithelial cells for the treatment of age-related macular degeneration
Petrus-Reurer S et al. Preclinical safety studies of human embryonic stem cell-derived retinal pigment epithelial cells for the treatment of age-related macular degeneration. . 2020-08-00. Pubmed ID: 32319201; DOI: 10.1002/sctm.19-0396; PMC: PMC7381808 KIe033-A 2020-08-00 2020-08-00 PubMed: 32319201 DOI: 10.1002/sctm.19-0396Associated cell lines:
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Samlali K, Ahmadi F, Quach ABV, Soffer G, Shih SCC
One Cell, One Drop, One Click: Hybrid Microfluidics for Mammalian Single Cell Isolation
Samlali K et al. One Cell, One Drop, One Click: Hybrid Microfluidics for Mammalian Single Cell Isolation. . 2020-08-00. Pubmed ID: 32705796; DOI: 10.1002/smll.202002400 KICRi002-AKICRi002-A-3 2020-08-00 2020-08-00 PubMed: 32705796 DOI: 10.1002/smll.202002400Associated cell lines:
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Gamu D, Gibson WT
Reciprocal skeletal phenotypes of PRC2-related overgrowth and Rubinstein-Taybi syndromes: potential role of H3K27 modifications
Gamu D et al. Reciprocal skeletal phenotypes of PRC2-related overgrowth and Rubinstein-Taybi syndromes: potential role of H3K27 modifications. . 2020-08-00. Pubmed ID: 32843427; DOI: 10.1101/mcs.a005058; PMC: PMC7476411 IAIi001-A 2020-08-00 2020-08-00 PubMed: 32843427 DOI: 10.1101/mcs.a005058Associated cell lines:
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Gois Beghini D, Iwao Horita S, Cascabulho CM, Anastácio Alves L, Henriques-Pons A
Induced Pluripotent Stem Cells: Hope in the Treatment of Diseases, including Muscular Dystrophies
Gois Beghini D et al. Induced Pluripotent Stem Cells: Hope in the Treatment of Diseases, including Muscular Dystrophies. . 2020-07-30. Pubmed ID: 32751747; DOI: 10.3390/ijms21155467; PMC: PMC7432218 FAMRCi006-AFAMRCi006-B 2020-07-30 2020-07-30 PubMed: 32751747 DOI: 10.3390/ijms21155467Associated cell lines:
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Patel A, Garcia Diaz A, Moore JC, Sirabella D, Corneo B
Establishment and characterization of two iPSC lines derived from healthy controls
Patel A et al. Establishment and characterization of two iPSC lines derived from healthy controls. . 2020-07-25. Pubmed ID: 32738631; DOI: 10.1016/j.scr.2020.101926 CUIMCi001-ACUIMCi002-A 2020-07-25 2020-07-25 PubMed: 32738631 DOI: 10.1016/j.scr.2020.101926Associated cell lines:
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Gusev K, Khudiakov A, Zaytseva A, Perepelina K, Makeenok S, Kaznacheyeva E, Kostareva A
Impact of the DSP-H1684R Genetic Variant on Ion Channels Activity in iPSC-Derived Cardiomyocytes
Gusev K et al. Impact of the DSP-H1684R Genetic Variant on Ion Channels Activity in iPSC-Derived Cardiomyocytes. . 2020-07-25. Pubmed ID: 32706220; DOI: 10.33594/000000249 FAMRCi004-AFAMRCi004-B 2020-07-25 2020-07-25 PubMed: 32706220 DOI: 10.33594/000000249Associated cell lines:
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D'Anzi A, Altieri F, Perciballi E, Ferrari D, Bernardini L, Goldoni M, Mazzini L, De Marchi F, Di Pierro A, D'Alfonso S, Gelati M, Vescovi AL, Rosati J
Generation of an induced pluripotent stem cell line, CSSi011-A (6534), from an Amyotrophic lateral sclerosis patient with heterozygous L145F mutation in SOD1 gene
D'Anzi A et al. Generation of an induced pluripotent stem cell line, CSSi011-A (6534), from an Amyotrophic lateral sclerosis patient with heterozygous L145F mutation in SOD1 gene. . 2020-07-25. Pubmed ID: 32739880; DOI: 10.1016/j.scr.2020.101924 CSSi011-A 2020-07-25 2020-07-25 PubMed: 32739880 DOI: 10.1016/j.scr.2020.101924Associated cell lines:
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Malakhova AA, Grigor'eva EV, Vasilyeva OY, Zhigalina DI, Skryabin NA, Sivtcev AA, Kolesnikov NA, Bueverov AO, Lebedev IN, Bogomolov PO, Zakian SM
Generation of two induced pluripotent stem cell lines from peripheral blood mononuclear cells of a patient with Wilson's disease
Malakhova AA et al. Generation of two induced pluripotent stem cell lines from peripheral blood mononuclear cells of a patient with Wilson's disease. . 2020-07-25. Pubmed ID: 32738633; DOI: 10.1016/j.scr.2020.101922 ICGi020-AICGi020-B 2020-07-25 2020-07-25 PubMed: 32738633 DOI: 10.1016/j.scr.2020.101922 -
Shahryari A, Moya N, Siehler J, Wang X, Karolina Blöchinger A, Burtscher I, Bakhti M, Mowla SJ, Lickert H
Generation of a human iPSC line harboring a biallelic large deletion at the INK4 locus (HMGUi001-A-5)
Shahryari A et al. Generation of a human iPSC line harboring a biallelic large deletion at the INK4 locus (HMGUi001-A-5). . 2020-07-25. Pubmed ID: 32739881; DOI: 10.1016/j.scr.2020.101927 HMGUi001-AHMGUi001-A-5 2020-07-25 2020-07-25 PubMed: 32739881 DOI: 10.1016/j.scr.2020.101927Associated cell lines:
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Feki A, Sloan-Béna F, Hibaoui Y
Parallel derivation of X-monosomy induced pluripotent stem cells (iPSCs) with isogenic control iPSCs
Feki A et al. Parallel derivation of X-monosomy induced pluripotent stem cells (iPSCs) with isogenic control iPSCs. . 2020-07-22. Pubmed ID: 32739879; DOI: 10.1016/j.scr.2020.101920 UNIGEi002-AUNIGEi004-A 2020-07-22 2020-07-22 PubMed: 32739879 DOI: 10.1016/j.scr.2020.101920Associated cell lines:
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Feyen DAM, McKeithan WL, Bruyneel AAN, Spiering S, Hörmann L, Ulmer B, Zhang H, Briganti F, Schweizer M, Hegyi B, Liao Z, Pölönen RP, Ginsburg KS, Lam CK, Serrano R, Wahlquist C, Kreymerman A, Vu M, Amatya PL, Behrens CS, Ranjbarvaziri S, Maas RGC, Greenhaw M, Bernstein D, Wu JC, Bers DM, Eschenhagen T, Metallo CM, Mercola M
Metabolic Maturation Media Improve Physiological Function of Human iPSC-Derived Cardiomyocytes
Feyen DAM et al. Metabolic Maturation Media Improve Physiological Function of Human iPSC-Derived Cardiomyocytes. . 2020-07-21. Pubmed ID: 32697997; DOI: 10.1016/j.celrep.2020.107925; PMC: PMC7437654 UKEi001-AUKEi003-AUKEi003-C 2020-07-21 2020-07-21 PubMed: 32697997 DOI: 10.1016/j.celrep.2020.107925 -
Chen X, Yang Y, Luo L, Xu L, Liu B, Jiang G, Hu X, Zeng Y, Wang Z
An iPSC line (TYWHSTi002-A) derived from a patient with Pendred syndrome caused by compound heterozygous mutations in the SLC26A4 gene
Chen X et al. An iPSC line (TYWHSTi002-A) derived from a patient with Pendred syndrome caused by compound heterozygous mutations in the SLC26A4 gene. . 2020-07-20. Pubmed ID: 32717573; DOI: 10.1016/j.scr.2020.101919 TYWHSTi002-A 2020-07-20 2020-07-20 PubMed: 32717573 DOI: 10.1016/j.scr.2020.101919Associated cell lines:
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Chen D, Li Z, Liu Y, Sampaio N, Yang D, Aksentijevich I, Boehm M, Chen G
Human induced pluripotent stem cells generated from a patient with a homozygous L272P mutation in the OTULIN gene (NIHTVBi014-A)
Chen D et al. Human induced pluripotent stem cells generated from a patient with a homozygous L272P mutation in the OTULIN gene (NIHTVBi014-A). . 2020-07-20. Pubmed ID: 32721894; DOI: 10.1016/j.scr.2020.101921; PMC: PMC7855794 NIHTVBi014-A 2020-07-20 2020-07-20 PubMed: 32721894 DOI: 10.1016/j.scr.2020.101921Associated cell lines:
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Filippo Buono M, von Boehmer L, Strang J, Hoerstrup SP, Emmert MY, Nugraha B
Human Cardiac Organoids for Modeling Genetic Cardiomyopathy
Filippo Buono M et al. Human Cardiac Organoids for Modeling Genetic Cardiomyopathy. . 2020-07-20. Pubmed ID: 32698471; DOI: 10.3390/cells9071733; PMC: PMC7409052 WTSIi020-AUKKi025-A 2020-07-20 2020-07-20 PubMed: 32698471 DOI: 10.3390/cells9071733Associated cell lines:
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Vaidyanath A, Khan M, Vaishnav B, Kakrani AL, Patil S, Shiras A
Development and characterization of two independent integration free iPSC clones NCCSi010-A and NCCSi010-B from a patient with alcoholic liver cirrhosis of Indian ethnicity
Vaidyanath A et al. Development and characterization of two independent integration free iPSC clones NCCSi010-A and NCCSi010-B from a patient with alcoholic liver cirrhosis of Indian ethnicity. . 2020-07-20. Pubmed ID: 32745713; DOI: 10.1016/j.scr.2020.101911 NCCSi010-ANCCSi010-B 2020-07-20 2020-07-20 PubMed: 32745713 DOI: 10.1016/j.scr.2020.101911Associated cell lines:
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Fukunaga I, Shirai K, Oe Y, Danzaki K, Ohta S, Shiga T, Chen C, Ikeda K, Akamatsu W, Kawano A, Kamiya K
Generation of two induced pluripotent stem cell lines from PBMCs of siblings carrying c.235delC mutation in the GJB2 gene associated with sensorineural hearing loss
Fukunaga I et al. Generation of two induced pluripotent stem cell lines from PBMCs of siblings carrying c.235delC mutation in the GJB2 gene associated with sensorineural hearing loss. . 2020-07-19. Pubmed ID: 32745712; DOI: 10.1016/j.scr.2020.101910 JUFMDOi005-AJUFMDOi006-A 2020-07-19 2020-07-19 PubMed: 32745712 DOI: 10.1016/j.scr.2020.101910Associated cell lines:
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Vallejo-Diez S, Fleischer A, María Martín-Fernández J, Sánchez-Gilabert A, Gómez-Martínez C, Castresana M, Bachiller D
Generation of one iPSC line (IMEDEAi007-A) by Sendai Virus transduction of PBMCs from a Psoriasis donor
Vallejo-Diez S et al. Generation of one iPSC line (IMEDEAi007-A) by Sendai Virus transduction of PBMCs from a Psoriasis donor. . 2020-07-17. Pubmed ID: 32707489; DOI: 10.1016/j.scr.2020.101917 IMEDEAi007-A 2020-07-17 2020-07-17 PubMed: 32707489 DOI: 10.1016/j.scr.2020.101917Associated cell lines:
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Vallejo-Diez S, Martín-Fernández JM, Sánchez-Gilabert A, Fleischer A, Gayá A, Castresana M, Bachiller D
Generation of a human iPSC line (IMEDEAi008-A) derived from natural homozygous CCR5-Δ32 PBMCs enriched in the pro-erythroblast population
Vallejo-Diez S et al. Generation of a human iPSC line (IMEDEAi008-A) derived from natural homozygous CCR5-Δ32 PBMCs enriched in the pro-erythroblast population. . 2020-07-17. Pubmed ID: 32702648; DOI: 10.1016/j.scr.2020.101918 IMEDEAi006-AIMEDEAi008-A 2020-07-17 2020-07-17 PubMed: 32702648 DOI: 10.1016/j.scr.2020.101918Associated cell lines:
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Xian Y, Xie Y, Song B, Ou Z, Ouyang S, Xie Y, Yang Y, Xiong Z, Li H, Sun X
The safety and effectiveness of genetically corrected iPSCs derived from β-thalassaemia patients in nonmyeloablative β-thalassaemic mice
Xian Y et al. The safety and effectiveness of genetically corrected iPSCs derived from β-thalassaemia patients in nonmyeloablative β-thalassaemic mice. . 2020-07-16. Pubmed ID: 32678022; DOI: 10.1186/s13287-020-01765-w; PMC: PMC7367314 GZHMUi001-A 2020-07-16 2020-07-16 PubMed: 32678022 DOI: 10.1186/s13287-020-01765-wAssociated cell lines:
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Zhang Y, Wang J, Zhou Y, Li H, Li A, Tan X, Wang G, Lei M
Generation of two induced pluripotent stem cell lines (XACHi0010-A, XACHi0011-A) from a Chinese family with combined oxidative phosphorylation deficiency carrying homozygous and heterozygous C1QBP-L275F mutation
Zhang Y et al. Generation of two induced pluripotent stem cell lines (XACHi0010-A, XACHi0011-A) from a Chinese family with combined oxidative phosphorylation deficiency carrying homozygous and heterozygous C1QBP-L275F mutation. . 2020-07-15. Pubmed ID: 32707487; DOI: 10.1016/j.scr.2020.101912 XACHi010-AXACHi011-A 2020-07-15 2020-07-15 PubMed: 32707487 DOI: 10.1016/j.scr.2020.101912Associated cell lines:
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Wei L, Zhang J, Chen D, Feng L, Wu C, Wang R, Li X
Generation of an integration-free induced pluripotent stem cell (iPSC) line (ZZUNEUi005-A) from a Wilson's disease patient harboring a homozygous Pro992Leu mutation in ATP7B gene
Wei L et al. Generation of an integration-free induced pluripotent stem cell (iPSC) line (ZZUNEUi005-A) from a Wilson's disease patient harboring a homozygous Pro992Leu mutation in ATP7B gene. . 2020-07-15. Pubmed ID: 32745714; DOI: 10.1016/j.scr.2020.101909 ZZUNEUi005-A 2020-07-15 2020-07-15 PubMed: 32745714 DOI: 10.1016/j.scr.2020.101909Associated cell lines:
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Niu S, Xiong H, Li Y, Zhang L
Generation of patient-specific induced pluripotent stem cells (ZZUSAHi001-A) derived from a familial atrial fibrillation patient carrying KCNA5 c.775G>A mutation
Niu S et al. Generation of patient-specific induced pluripotent stem cells (ZZUSAHi001-A) derived from a familial atrial fibrillation patient carrying KCNA5 c.775G>A mutation. . 2020-07-15. Pubmed ID: 32721895; DOI: 10.1016/j.scr.2020.101915 ZZUSAHi001-A 2020-07-15 2020-07-15 PubMed: 32721895 DOI: 10.1016/j.scr.2020.101915Associated cell lines:
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Naumovska E, Aalderink G, Wong Valencia C, Kosim K, Nicolas A, Brown S, Vulto P, Erdmann KS, Kurek D
Direct On-Chip Differentiation of Intestinal Tubules from Induced Pluripotent Stem Cells
Naumovska E et al. Direct On-Chip Differentiation of Intestinal Tubules from Induced Pluripotent Stem Cells. . 2020-07-14. Pubmed ID: 32674311; DOI: 10.3390/ijms21144964; PMC: PMC7404294 UOSi001-A 2020-07-14 2020-07-14 PubMed: 32674311 DOI: 10.3390/ijms21144964Associated cell lines:
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Lee SJ, Kang KW, Kim JH, Park Y, Kim BS
Generation of an induced pluripotent stem cell line KUMCi001-A from CD34+ bone marrow cells of a patient with acute lymphoblastic leukemia using human placenta-derived cell conditioned medium
Lee SJ et al. Generation of an induced pluripotent stem cell line KUMCi001-A from CD34+ bone marrow cells of a patient with acute lymphoblastic leukemia using human placenta-derived cell conditioned medium. . 2020-07-13. Pubmed ID: 32707488; DOI: 10.1016/j.scr.2020.101913 KUMCi001-A 2020-07-13 2020-07-13 PubMed: 32707488 DOI: 10.1016/j.scr.2020.101913Associated cell lines:
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Yi T, Bai R, Sun H, Lan F, Zhang H, He Y
Generation of a NONO homozygous knockout human induced pluripotent stem cell line by CRISPR/Cas9 editing
Yi T et al. Generation of a NONO homozygous knockout human induced pluripotent stem cell line by CRISPR/Cas9 editing. . 2020-07-08. Pubmed ID: 32717574; DOI: 10.1016/j.scr.2020.101893 CMUi002-ACMUi002-A-1 2020-07-08 2020-07-08 PubMed: 32717574 DOI: 10.1016/j.scr.2020.101893Associated cell lines:
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Gutbier S, Wanke F, Dahm N, Rümmelin A, Zimmermann S, Christensen K, Köchl F, Rautanen A, Hatje K, Geering B, Zhang JD, Britschgi M, Cowley SA, Patsch C
Large-Scale Production of Human iPSC-Derived Macrophages for Drug Screening
Gutbier S et al. Large-Scale Production of Human iPSC-Derived Macrophages for Drug Screening. . 2020-07-07. Pubmed ID: 32645954; DOI: 10.3390/ijms21134808; PMC: PMC7370446 STBCi024-BSTBCi026-B 2020-07-07 2020-07-07 PubMed: 32645954 DOI: 10.3390/ijms21134808Associated cell lines:
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Bodda C, Reinert LS, Fruhwürth S, Richardo T, Sun C, Zhang BC, Kalamvoki M, Pohlmann A, Mogensen TH, Bergström P, Agholme L, O'Hare P, Sodeik B, Gyrd-Hansen M, Zetterberg H, Paludan SR
HSV1 VP1-2 deubiquitinates STING to block type I interferon expression and promote brain infection
Bodda C et al. HSV1 VP1-2 deubiquitinates STING to block type I interferon expression and promote brain infection. . 2020-07-06. Pubmed ID: 32383759; DOI: 10.1084/jem.20191422; PMC: PMC7336311 WTSIi015-A 2020-07-06 2020-07-06 PubMed: 32383759 DOI: 10.1084/jem.20191422Associated cell lines:
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Nengqing L, Dian L, Yingjun X, Yi C, Lina H, Diyu C, Yinghong Y, Bing S, Xiaofang S
Generation of induced pluripotent stem cell GZHMCi001-A and GZHMCi001-B derived from peripheral blood mononuclear cells of epileptic patients with KCNC1 mutation
Nengqing L et al. Generation of induced pluripotent stem cell GZHMCi001-A and GZHMCi001-B derived from peripheral blood mononuclear cells of epileptic patients with KCNC1 mutation. . 2020-07-05. Pubmed ID: 32712483; DOI: 10.1016/j.scr.2020.101897 GZHMCi001-AGZHMCi001-B 2020-07-05 2020-07-05 PubMed: 32712483 DOI: 10.1016/j.scr.2020.101897Associated cell lines:
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Zheng Z, Lu W, Pei Z, Chen J, Yang T, Luo F
Generation of an induced pluripotent stem cell line (CHFUi001-A) from an osteogenesis imperfecta patient with COL1A2 mutation
Zheng Z et al. Generation of an induced pluripotent stem cell line (CHFUi001-A) from an osteogenesis imperfecta patient with COL1A2 mutation. . 2020-07-05. Pubmed ID: 32659730; DOI: 10.1016/j.scr.2020.101907 FDCHi004-A 2020-07-05 2020-07-05 PubMed: 32659730 DOI: 10.1016/j.scr.2020.101907Associated cell lines:
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Ababneh NA, Al-Kurdi B, Ali D, Abuarqoub D, Barham R, Ryalat AT, Awidi A
Establishment of (JUCTCi007-A) iPSC line from a patient with congenital myasthenic syndrome (CMS) carrying a homozygous mutation p.Arg331Trp (c.991C > T) in the CHRNE gene
Ababneh NA et al. Establishment of (JUCTCi007-A) iPSC line from a patient with congenital myasthenic syndrome (CMS) carrying a homozygous mutation p.Arg331Trp (c.991C > T) in the CHRNE gene. . 2020-07-03. Pubmed ID: 32645605; DOI: 10.1016/j.scr.2020.101906 JUCTCi007-A 2020-07-03 2020-07-03 PubMed: 32645605 DOI: 10.1016/j.scr.2020.101906Associated cell lines:
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Yan Y, Wu S, Jiang L, Yang B, Chen X, Liu Y, Yu B, Fu J, Yu J, Ning H, Chu M, Yang J
Generation of a human iPSC line CIBi007-A from a patient with young-onset Parkinson's disease carrying variants in PRKN and HTRA2
Yan Y et al. Generation of a human iPSC line CIBi007-A from a patient with young-onset Parkinson's disease carrying variants in PRKN and HTRA2. . 2020-07-03. Pubmed ID: 32688332; DOI: 10.1016/j.scr.2020.101905 CIBi007-A 2020-07-03 2020-07-03 PubMed: 32688332 DOI: 10.1016/j.scr.2020.101905Associated cell lines:
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Buikema JW, Lee S, Goodyer WR, Maas RG, Chirikian O, Li G, Miao Y, Paige SL, Lee D, Wu H, Paik DT, Rhee S, Tian L, Galdos FX, Puluca N, Beyersdorf B, Hu J, Beck A, Venkamatran S, Swami S, Wijnker P, Schuldt M, Dorsch LM, van Mil A, Red-Horse K, Wu JY, Geisen C, Hesse M, Serpooshan V, Jovinge S, Fleischmann BK, Doevendans PA, van der Velden J, Garcia KC, Wu JC, Sluijter JPG, Wu SM
Wnt Activation and Reduced Cell-Cell Contact Synergistically Induce Massive Expansion of Functional Human iPSC-Derived Cardiomyocytes
Buikema JW et al. Wnt Activation and Reduced Cell-Cell Contact Synergistically Induce Massive Expansion of Functional Human iPSC-Derived Cardiomyocytes. . 2020-07-02. Pubmed ID: 32619518; DOI: 10.1016/j.stem.2020.06.001; PMC: PMC7334437 BIHi050-A 2020-07-02 2020-07-02 PubMed: 32619518 DOI: 10.1016/j.stem.2020.06.001Associated cell lines:
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Rebs S, Sedaghat-Hamedani F, Kayvanpour E, Meder B, Streckfuss-Bömeke K
Generation of pluripotent stem cell lines and CRISPR/Cas9 modified isogenic controls from a patient with dilated cardiomyopathy harboring a RBM20 p.R634W mutation
Rebs S et al. Generation of pluripotent stem cell lines and CRISPR/Cas9 modified isogenic controls from a patient with dilated cardiomyopathy harboring a RBM20 p.R634W mutation. . 2020-07-02. Pubmed ID: 32674065; DOI: 10.1016/j.scr.2020.101901 UMGi144-AUMGi144-A-1 2020-07-02 2020-07-02 PubMed: 32674065 DOI: 10.1016/j.scr.2020.101901Associated cell lines:
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Lemme M, Braren I, Prondzynski M, Aksehirlioglu B, Ulmer BM, Schulze ML, Ismaili D, Meyer C, Hansen A, Christ T, Lemoine MD, Eschenhagen T
Chronic intermittent tachypacing by an optogenetic approach induces arrhythmia vulnerability in human engineered heart tissue
Lemme M et al. Chronic intermittent tachypacing by an optogenetic approach induces arrhythmia vulnerability in human engineered heart tissue. . 2020-07-01. Pubmed ID: 31598634; DOI: 10.1093/cvr/cvz245; PMC: PMC7314638 UKEi001-A 2020-07-01 2020-07-01 PubMed: 31598634 DOI: 10.1093/cvr/cvz245Associated cell lines:
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Wang J, Su J, Gong T, Li T, Shen J, Wang H, Xie H, Zhou L, Zheng S, Liang P
Generation of ZJUi003-A, an induced pluripotent stem cell line from a Wilson's disease patient carrying a c.180_181del mutation in ATP7B gene
Wang J et al. Generation of ZJUi003-A, an induced pluripotent stem cell line from a Wilson's disease patient carrying a c.180_181del mutation in ATP7B gene. . 2020-07-00. Pubmed ID: 32534167; DOI: 10.1016/j.scr.2020.101873 ZJUi003-A 2020-07-00 2020-07-00 PubMed: 32534167 DOI: 10.1016/j.scr.2020.101873Associated cell lines:
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Gauthier-Fisher A, Kauffman A, Librach CL
Potential use of stem cells for fertility preservation
Gauthier-Fisher A et al. Potential use of stem cells for fertility preservation. . 2020-07-00. Pubmed ID: 31560823; DOI: 10.1111/andr.12713 MUSIi006-A 2020-07-00 2020-07-00 PubMed: 31560823 DOI: 10.1111/andr.12713Associated cell lines:
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Dahlmann J, Sahabian A, Drick N, Haase A, Göhring G, Lachmann N, Ringshausen FC, Welte T, Martin U, Olmer R
Generation of two hiPSC lines (MHHi016-A, MHHi016-B) from a primary ciliary dyskinesia patient carrying a homozygous 5 bp duplication (c.248_252dup (p.Gly85Cysfs*11)) in exon 1 of the CCNO gene
Dahlmann J et al. Generation of two hiPSC lines (MHHi016-A, MHHi016-B) from a primary ciliary dyskinesia patient carrying a homozygous 5 bp duplication (c.248_252dup (p.Gly85Cysfs*11)) in exon 1 of the CCNO gene. . 2020-07-00. Pubmed ID: 32464346; DOI: 10.1016/j.scr.2020.101850 MHHi016-AMHHi016-B 2020-07-00 2020-07-00 PubMed: 32464346 DOI: 10.1016/j.scr.2020.101850 -
Han MJ, Annunziata I, Weesner J, Campos Y, Salie M, O'Reilly C, d'Azzo A
Generation of human induced pluripotent stem cells (hIPSCs) from sialidosis types I and II patients with pathogenic neuraminidase 1 mutations
Han MJ et al. Generation of human induced pluripotent stem cells (hIPSCs) from sialidosis types I and II patients with pathogenic neuraminidase 1 mutations. . 2020-07-00. Pubmed ID: 32485644; DOI: 10.1016/j.scr.2020.101836; PMC: PMC7446138 STJUDEi001-ASTJUDEi002-ASTJUDEi003-A 2020-07-00 2020-07-00 PubMed: 32485644 DOI: 10.1016/j.scr.2020.101836Associated cell lines:
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Drick N, Dahlmann J, Sahabian A, Haase A, Göhring G, Lachmann N, Ringshausen FC, Welte T, Martin U, Olmer R
Generation of two human induced pluripotent stem cell lines (MHHi017-A, MHHi017-B) from a patient with primary ciliary dyskinesia carrying a homozygous mutation (c.7915C > T [p.Arg2639*]) in the DNAH5 gene
Drick N et al. Generation of two human induced pluripotent stem cell lines (MHHi017-A, MHHi017-B) from a patient with primary ciliary dyskinesia carrying a homozygous mutation (c.7915C > T [p.Arg2639*]) in the DNAH5 gene. . 2020-07-00. Pubmed ID: 32470793; DOI: 10.1016/j.scr.2020.101848 MHHi017-AMHHi017-B 2020-07-00 2020-07-00 PubMed: 32470793 DOI: 10.1016/j.scr.2020.101848 -
Meraviglia V, Arendzen CH, Tok M, Freund C, Maione AS, Sommariva E, Bellin M
Generation of human induced pluripotent stem cell line LUMCi027-A and its isogenic gene-corrected line from a patient affected by arrhythmogenic cardiomyopathy and carrying the c.2013delC PKP2 mutation
Meraviglia V et al. Generation of human induced pluripotent stem cell line LUMCi027-A and its isogenic gene-corrected line from a patient affected by arrhythmogenic cardiomyopathy and carrying the c.2013delC PKP2 mutation. . 2020-07-00. Pubmed ID: 32485643; DOI: 10.1016/j.scr.2020.101835 LUMCi027-ALUMCi027-A-1 2020-07-00 2020-07-00 PubMed: 32485643 DOI: 10.1016/j.scr.2020.101835Associated cell lines:
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Fan C, Shah Z, Ullah H, Philonenko ES, Zhang B, Tan Y, Wang C, Zhang J, Samokhvalov IM
TALEN-mediated biallelic inactivation of MYB in human embryonic stem cell lines WAe001-A-45 and WAe001-A-46
Fan C et al. TALEN-mediated biallelic inactivation of MYB in human embryonic stem cell lines WAe001-A-45 and WAe001-A-46. . 2020-07-00. Pubmed ID: 32526676; DOI: 10.1016/j.scr.2020.101854 WAe001-AWAe001-A-45WAe001-A-46 2020-07-00 2020-07-00 PubMed: 32526676 DOI: 10.1016/j.scr.2020.101854Associated cell lines:
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Chen J, Yang X, Fu B, Zhu P, Zhu Y, Guo X, Sha J, Yuan Y
Generation of human induced pluripotent stem cell (SKLRMi001-A) from a patient with partial androgen insensitivity syndrome (PAIS)
Chen J et al. Generation of human induced pluripotent stem cell (SKLRMi001-A) from a patient with partial androgen insensitivity syndrome (PAIS). . 2020-07-00. Pubmed ID: 32505105; DOI: 10.1016/j.scr.2020.101863 SKLRMi001-A 2020-07-00 2020-07-00 PubMed: 32505105 DOI: 10.1016/j.scr.2020.101863Associated cell lines:
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Mui BWH, Arora D, Mallon BS, Martinez AF, Lee JS, Muenke M, Kruszka P, Kidwai FK, Robey PG
Generation of human induced pluripotent stem cell line (NIDCRi001-A) from a Muenke syndrome patient with an FGFR3 p.Pro250Arg mutation
Mui BWH et al. Generation of human induced pluripotent stem cell line (NIDCRi001-A) from a Muenke syndrome patient with an FGFR3 p.Pro250Arg mutation. . 2020-07-00. Pubmed ID: 32505898; DOI: 10.1016/j.scr.2020.101823; PMC: PMC8447220 NIDCRi001-A 2020-07-00 2020-07-00 PubMed: 32505898 DOI: 10.1016/j.scr.2020.101823Associated cell lines:
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Hepburn AC, Curry EL, Moad M, Steele RE, Franco OE, Wilson L, Singh P, Buskin A, Crawford SE, Gaughan L, Mills IG, Hayward SW, Robson CN, Heer R
Propagation of human prostate tissue from induced pluripotent stem cells
Hepburn AC et al. Propagation of human prostate tissue from induced pluripotent stem cells. . 2020-07-00. Pubmed ID: 32170918; DOI: 10.1002/sctm.19-0286; PMC: PMC7308643 IBPi002-A 2020-07-00 2020-07-00 PubMed: 32170918 DOI: 10.1002/sctm.19-0286Associated cell lines:
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Kim KP, Yoon J, Shin B, Röpke A, Han DW, Schöler HR
Generation of a human iPSC line (MPIi006-A) from a patient with Pelizaeus-Merzbacher disease
Kim KP et al. Generation of a human iPSC line (MPIi006-A) from a patient with Pelizaeus-Merzbacher disease. . 2020-07-00. Pubmed ID: 32446239; DOI: 10.1016/j.scr.2020.101839 MPIi006-A 2020-07-00 2020-07-00 PubMed: 32446239 DOI: 10.1016/j.scr.2020.101839Associated cell lines:
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Shi L, Cui Y, Qi Z, Zhou X, Luan J, Han J
Generation of two non-integrated induced pluripotent stem cell lines from urine-derived cells of a Chinese patient carrying NF1 gene mutation
Shi L et al. Generation of two non-integrated induced pluripotent stem cell lines from urine-derived cells of a Chinese patient carrying NF1 gene mutation. . 2020-07-00. Pubmed ID: 32554297; DOI: 10.1016/j.scr.2020.101842 SMBCi003-ASMBCi003-B 2020-07-00 2020-07-00 PubMed: 32554297 DOI: 10.1016/j.scr.2020.101842Associated cell lines:
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Hu J, Lu C, Zhu W, Jiang Q, Du W, Wu N
Establishment of an induced pluripotent stem cell line (SHFDi001-A) from a patient with ankylosing spondylitis
Hu J et al. Establishment of an induced pluripotent stem cell line (SHFDi001-A) from a patient with ankylosing spondylitis. . 2020-07-00. Pubmed ID: 32570173; DOI: 10.1016/j.scr.2020.101879 SHFDi001-A 2020-07-00 2020-07-00 PubMed: 32570173 DOI: 10.1016/j.scr.2020.101879Associated cell lines:
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Schöning L, Loges NT, Nitschke Y, Höben IM, Röpke A, Crisponi L, Omran H, Rutsch F, Buers I
Generation of induced pluripotent stem cell lines from a Crisponi/Cold induced sweating syndrome type 1 individual
Schöning L et al. Generation of induced pluripotent stem cell lines from a Crisponi/Cold induced sweating syndrome type 1 individual. . 2020-07-00. Pubmed ID: 32492556; DOI: 10.1016/j.scr.2020.101820 UKMi001-AUKMi001-BUKMi001-C 2020-07-00 2020-07-00 PubMed: 32492556 DOI: 10.1016/j.scr.2020.101820 -
Na DH, Lim SW, Kim BM, Kim KW, Shin YJ, Chae H, Ko EJ, Yang CW, Kim M, Chung BH
Generation of a human induced pluripotent stem cell line (CMCi001-A) from a patient with karyomegalic interstitial nephritis with homozygous frameshift deletion mutation c.1985_1994del10 of the FANCD2/FANCI-Associated Nuclease 1 gene
Na DH et al. Generation of a human induced pluripotent stem cell line (CMCi001-A) from a patient with karyomegalic interstitial nephritis with homozygous frameshift deletion mutation c.1985_1994del10 of the FANCD2/FANCI-Associated Nuclease 1 gene. . 2020-07-00. Pubmed ID: 32563974; DOI: 10.1016/j.scr.2020.101876 CMCi001-A 2020-07-00 2020-07-00 PubMed: 32563974 DOI: 10.1016/j.scr.2020.101876Associated cell lines:
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Sawada T, Benjamin KJM, Brandtjen AC, Tietze E, Allen SJ, Paquola ACM, Kleinman JE, Hyde TM, Erwin JA
Generation of four postmortem dura-derived iPS cell lines from four control individuals with genotypic and brain-region-specific transcriptomic data available through the BrainSEQ consortium
Sawada T et al. Generation of four postmortem dura-derived iPS cell lines from four control individuals with genotypic and brain-region-specific transcriptomic data available through the BrainSEQ consortium. . 2020-07-00. Pubmed ID: 32446240; DOI: 10.1016/j.scr.2020.101806; PMC: PMC10515715 LIBDi002-ALIBDi006-ALIBDi007-ALIBDi009-A 2020-07-00 2020-07-00 PubMed: 32446240 DOI: 10.1016/j.scr.2020.101806Associated cell lines:
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Janz A, Chen R, Regensburger M, Ueda Y, Rost S, Klopocki E, Günther K, Edenhofer F, Duff HJ, Ergün S, Gerull B
Generation of two patient-derived iPSC lines from siblings (LIBUCi001-A and LIBUCi002-A) and a genetically modified iPSC line (JMUi001-A-1) to mimic dilated cardiomyopathy with ataxia (DCMA) caused by a homozygous DNAJC19 mutation
Janz A et al. Generation of two patient-derived iPSC lines from siblings (LIBUCi001-A and LIBUCi002-A) and a genetically modified iPSC line (JMUi001-A-1) to mimic dilated cardiomyopathy with ataxia (DCMA) caused by a homozygous DNAJC19 mutation. . 2020-07-00. Pubmed ID: 32521499; DOI: 10.1016/j.scr.2020.101856 LIBUCi001-ALIBUCi002-AJMUi001-AJMUi001-A-1 2020-07-00 2020-07-00 PubMed: 32521499 DOI: 10.1016/j.scr.2020.101856Associated cell lines:
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Kamand M, Ilieva M, Forsberg SL, Thomassen M, Fex Svenningsen Å, Holst B, Meyer M, Michel TM
Generation of human induced pluripotent stem cells (SDUKIi002-A) from a 22-year-old male diagnosed with autism spectrum disorder
Kamand M et al. Generation of human induced pluripotent stem cells (SDUKIi002-A) from a 22-year-old male diagnosed with autism spectrum disorder. . 2020-07-00. Pubmed ID: 32447258; DOI: 10.1016/j.scr.2020.101834 SDUKIi002-A 2020-07-00 2020-07-00 PubMed: 32447258 DOI: 10.1016/j.scr.2020.101834Associated cell lines:
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Zhao H, He L, Li S, Huang H, Tang F, Han X, Lin Z, Tian C, Huang R, Zhou P, Huang J, Deng S, Li Z
Generation of corrected-hiPSC (USTCi001-A-1) from epilepsy patient iPSCs using TALEN-mediated editing of the SCN1A gene
Zhao H et al. Generation of corrected-hiPSC (USTCi001-A-1) from epilepsy patient iPSCs using TALEN-mediated editing of the SCN1A gene. . 2020-07-00. Pubmed ID: 32544858; DOI: 10.1016/j.scr.2020.101864 USTCi001-AUSTCi001-A-1 2020-07-00 2020-07-00 PubMed: 32544858 DOI: 10.1016/j.scr.2020.101864Associated cell lines:
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Yoshida S, Okura H, Suga H, Nishitomi T, Sakurai A, Arima H, Matsuyama A
Generation of three induced pluripotent stem cell (iPSC) lines from a multiple endocrine neoplasia type 1 (MEN1) patient and three iPSC lines from an unaffected relative of the patient
Yoshida S et al. Generation of three induced pluripotent stem cell (iPSC) lines from a multiple endocrine neoplasia type 1 (MEN1) patient and three iPSC lines from an unaffected relative of the patient. . 2020-07-00. Pubmed ID: 32460232; DOI: 10.1016/j.scr.2020.101846 FHUi001-AFHUi002-AFHUi001-BFHUi001-CFHUi002-BFHUi002-C 2020-07-00 2020-07-00 PubMed: 32460232 DOI: 10.1016/j.scr.2020.101846 -
Wang A, Xi J, Yuan F, Wang Y, Wang S, Wang C, Wang C, Lin L, Luo X, Xu Q, Yin R, Cheng H, Zhang Y, Sun X, Yang J, Yan J, Zeng F, Chen Y
Generation of an induced pluripotent stem cell line (SHCDNi003-A) from a one-year-old Chinese Han infant with Allan-Herndon-Dudley syndrome
Wang A et al. Generation of an induced pluripotent stem cell line (SHCDNi003-A) from a one-year-old Chinese Han infant with Allan-Herndon-Dudley syndrome. . 2020-07-00. Pubmed ID: 32603881; DOI: 10.1016/j.scr.2020.101872 SHCDNi003-A 2020-07-00 2020-07-00 PubMed: 32603881 DOI: 10.1016/j.scr.2020.101872Associated cell lines:
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Buers I, Schöning L, Tomas Loges N, Nitschke Y, Höben IM, Röpke A, Crisponi L, Omran H, Rutsch F
Crisponi syndrome/cold-induced sweating syndrome type 2: Reprogramming of CS/CISS2 individual derived fibroblasts into three clones of one iPSC line
Buers I et al. Crisponi syndrome/cold-induced sweating syndrome type 2: Reprogramming of CS/CISS2 individual derived fibroblasts into three clones of one iPSC line. . 2020-07-00. Pubmed ID: 32512309; DOI: 10.1016/j.scr.2020.101855 UKMi002-A 2020-07-00 2020-07-00 PubMed: 32512309 DOI: 10.1016/j.scr.2020.101855Associated cell lines:
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Menara G, Lefort N, Antignac C, Mollet G
Generation of an induced pluripotent stem cell (iPSC) line (IMAGINi007) from a patient with steroid-resistant nephrotic syndrome carrying the homozygous p.R138Q mutation in the podocin-encoding NPHS2 gene
Menara G et al. Generation of an induced pluripotent stem cell (iPSC) line (IMAGINi007) from a patient with steroid-resistant nephrotic syndrome carrying the homozygous p.R138Q mutation in the podocin-encoding NPHS2 gene. . 2020-07-00. Pubmed ID: 32585588; DOI: 10.1016/j.scr.2020.101878 IMAGINi007-A 2020-07-00 2020-07-00 PubMed: 32585588 DOI: 10.1016/j.scr.2020.101878Associated cell lines:
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Deng X, Iwagawa T, Fukushima M, Watanabe S
Characterization of human-induced pluripotent stem cells carrying homozygous RB1 gene deletion
Deng X et al. Characterization of human-induced pluripotent stem cells carrying homozygous RB1 gene deletion. . 2020-07-00. Pubmed ID: 32277725; DOI: 10.1111/gtc.12771 VRFi001-A 2020-07-00 2020-07-00 PubMed: 32277725 DOI: 10.1111/gtc.12771Associated cell lines:
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Bouma MJ, Orlova V, van den Hil FE, Mager HJ, Baas F, de Knijff P, Mummery CL, Mikkers H, Freund C
Generation and genetic repair of 2 iPSC clones from a patient bearing a heterozygous c.1120del18 mutation in the ACVRL1 gene leading to Hereditary Hemorrhagic Telangiectasia (HHT) type 2
Bouma MJ et al. Generation and genetic repair of 2 iPSC clones from a patient bearing a heterozygous c.1120del18 mutation in the ACVRL1 gene leading to Hereditary Hemorrhagic Telangiectasia (HHT) type 2. . 2020-07-00. Pubmed ID: 32485642; DOI: 10.1016/j.scr.2020.101786 LUMCi030-ALUMCi030-BLUMCi030-A-1LUMCi030-B-1 2020-07-00 2020-07-00 PubMed: 32485642 DOI: 10.1016/j.scr.2020.101786Associated cell lines:
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Lacassie Y, Johnson B, Lay-Son G, Quintana R, King A, Cortes F, Alvarez C, Gomez R, Vargas A, Chalew S, King A, Guardia S, Sorensen RU, Aradhya S
Severe SOPH syndrome due to a novel NBAS mutation in a 27-year-old woman-Review of this pleiotropic, autosomal recessive disorder: Mystery solved after two decades
Lacassie Y et al. Severe SOPH syndrome due to a novel NBAS mutation in a 27-year-old woman-Review of this pleiotropic, autosomal recessive disorder: Mystery solved after two decades. . 2020-07-00. Pubmed ID: 32297715; DOI: 10.1002/ajmg.a.61597 DHMCi004-A 2020-07-00 2020-07-00 PubMed: 32297715 DOI: 10.1002/ajmg.a.61597Associated cell lines:
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Grzela DP, Marciniak B, Pulaski L
Characterization of an induced pluripotent stem cell line (IMBPASi001-A) derived from fibroblasts of a patient affected by Wolfram Syndrome
Grzela DP et al. Characterization of an induced pluripotent stem cell line (IMBPASi001-A) derived from fibroblasts of a patient affected by Wolfram Syndrome. . 2020-07-00. Pubmed ID: 32521500; DOI: 10.1016/j.scr.2020.101858 IMBPASi001-A 2020-07-00 2020-07-00 PubMed: 32521500 DOI: 10.1016/j.scr.2020.101858Associated cell lines:
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Li Y, Ibañez DP, Fan W, Zhao P, Chen S, Md Abdul M, Jiang Y, Fu L, Luo Z, Liu Z, Yang Y, Guo J, Volpe G, Kanwal S, Wang D, Tang B, Li W
Generation of an induced pluripotent stem cell line (GIBHi004-A) from a Parkinson's disease patient with mutant DJ-1/PARK7 (p.L10P)
Li Y et al. Generation of an induced pluripotent stem cell line (GIBHi004-A) from a Parkinson's disease patient with mutant DJ-1/PARK7 (p.L10P). . 2020-07-00. Pubmed ID: 32534165; DOI: 10.1016/j.scr.2020.101845 GIBHi004-A 2020-07-00 2020-07-00 PubMed: 32534165 DOI: 10.1016/j.scr.2020.101845Associated cell lines:
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Arbini A, Gilmore J, King MD, Gorman KM, Krawczyk J, McInerney V, O'Brien T, Shen S, Allen NM
Generation of three induced pluripotent stem cell (iPSC) lines from a patient with developmental epileptic encephalopathy due to the pathogenic KCNA2 variant c.869T>G; p.Leu290Arg (NUIGi052-A, NUIGi052-B, NUIGi052-C)
Arbini A et al. Generation of three induced pluripotent stem cell (iPSC) lines from a patient with developmental epileptic encephalopathy due to the pathogenic KCNA2 variant c.869T>G; p.Leu290Arg (NUIGi052-A, NUIGi052-B, NUIGi052-C). . 2020-07-00. Pubmed ID: 32540721; DOI: 10.1016/j.scr.2020.101853 NUIGi052-ANUIGi052-BNUIGi052-C 2020-07-00 2020-07-00 PubMed: 32540721 DOI: 10.1016/j.scr.2020.101853Associated cell lines:
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Dementyeva EV, Kovalenko VR, Zhiven MK, Ustyantseva EI, Kretov EI, Vyatkin YV, Zakian SM
Generation of two clonal iPSC lines, ICGi019-A and ICGi019-B, by reprogramming peripheral blood mononuclear cells of a patient suffering from hypertrophic cardiomyopathy and carrying a heterozygous p.M659I mutation in MYH7
Dementyeva EV et al. Generation of two clonal iPSC lines, ICGi019-A and ICGi019-B, by reprogramming peripheral blood mononuclear cells of a patient suffering from hypertrophic cardiomyopathy and carrying a heterozygous p.M659I mutation in MYH7. . 2020-07-00. Pubmed ID: 32422568; DOI: 10.1016/j.scr.2020.101840 ICGi019-AICGi019-B 2020-07-00 2020-07-00 PubMed: 32422568 DOI: 10.1016/j.scr.2020.101840 -
Toombs J, Panther L, Ornelas L, Liu C, Gomez E, Martín-Ibáñez R, Cox SR, Ritchie SJ, Harris SE, Taylor A, Redmond P, Russ TC, Murphy L, Cooper JD, Burr K, Selvaraj BT, Browne C, Svendsen CN, Cowley SA, Deary IJ, Chandran S, Spires-Jones TL, Sareen D
Generation of twenty four induced pluripotent stem cell lines from twenty four members of the Lothian Birth Cohort 1936
Toombs J et al. Generation of twenty four induced pluripotent stem cell lines from twenty four members of the Lothian Birth Cohort 1936. . 2020-07-00. Pubmed ID: 32450543; DOI: 10.1016/j.scr.2020.101851; PMC: PMC7347008 EDi021-AEDi022-AEDi023-AEDi024-AEDi025-AEDi026-AEDi027-AEDi028-AEDi029-AEDi030-AEDi031-AEDi032-AEDi033-AEDi034-AEDi035-AEDi036-AEDi037-AEDi038-AEDi039-AEDi040-AEDi041-AEDi042-AEDi043-AEDi044-AEDi045-A 2020-07-00 2020-07-00 PubMed: 32450543 DOI: 10.1016/j.scr.2020.101851 -
Kim BY, Lee JS, Kim YO, Koo SK, Park MH
Generation of induced pluripotent stem cells (KSCBi009-A) from a patient with Prader-Willi syndrome (PWS) featuring deletion of the paternal chromosome region 15q11.2-q13
Kim BY et al. Generation of induced pluripotent stem cells (KSCBi009-A) from a patient with Prader-Willi syndrome (PWS) featuring deletion of the paternal chromosome region 15q11.2-q13. . 2020-07-00. Pubmed ID: 32474395; DOI: 10.1016/j.scr.2020.101847 KSCBi009-A 2020-07-00 2020-07-00 PubMed: 32474395 DOI: 10.1016/j.scr.2020.101847Associated cell lines:
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Zulueta A, Mingione A, Signorelli P, Caretti A, Ghidoni R, Trinchera M
Simple and Complex Sugars in Parkinson's Disease: a Bittersweet Taste
Zulueta A et al. Simple and Complex Sugars in Parkinson's Disease: a Bittersweet Taste. . 2020-07-00. Pubmed ID: 32430844; DOI: 10.1007/s12035-020-01931-4 ICCSICi005-A 2020-07-00 2020-07-00 PubMed: 32430844 DOI: 10.1007/s12035-020-01931-4Associated cell lines:
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Zhang SJ, Lian TY, Zhu XJ, Lu D, Xu XQ, Jiang X, Jing ZC
Derivation of an induced pluripotent stem cell line (PUMCHi003-A) from a patient with pulmonary arterial hypertension carrying heterozygous mutation in PTGIS gene
Zhang SJ et al. Derivation of an induced pluripotent stem cell line (PUMCHi003-A) from a patient with pulmonary arterial hypertension carrying heterozygous mutation in PTGIS gene. . 2020-07-00. Pubmed ID: 32559633; DOI: 10.1016/j.scr.2020.101875 PUMCHi003-A 2020-07-00 2020-07-00 PubMed: 32559633 DOI: 10.1016/j.scr.2020.101875Associated cell lines:
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Moya N, Shahryari A, Burtscher I, Beckenbauer J, Bakhti M, Lickert H
Generation of a homozygous ARX nuclear CFP (ARX(nCFP/nCFP)) reporter human iPSC line (HMGUi001-A-4)
Moya N et al. Generation of a homozygous ARX nuclear CFP (ARX(nCFP/nCFP)) reporter human iPSC line (HMGUi001-A-4). . 2020-07-00. Pubmed ID: 32544857; DOI: 10.1016/j.scr.2020.101874 HMGUi001-AHMGUi001-A-4 2020-07-00 2020-07-00 PubMed: 32544857 DOI: 10.1016/j.scr.2020.101874Associated cell lines:
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Collado MS, Armstrong AJ, Olson M, Hoang SA, Day N, Summar M, Chapman KA, Reardon J, Figler RA, Wamhoff BR
Biochemical and anaplerotic applications of in vitro models of propionic acidemia and methylmalonic acidemia using patient-derived primary hepatocytes
Collado MS et al. Biochemical and anaplerotic applications of in vitro models of propionic acidemia and methylmalonic acidemia using patient-derived primary hepatocytes. . 2020-07-00. Pubmed ID: 32451238; DOI: 10.1016/j.ymgme.2020.05.003; PMC: PMC7337260 UAMi004-A 2020-07-00 2020-07-00 PubMed: 32451238 DOI: 10.1016/j.ymgme.2020.05.003Associated cell lines:
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Wang Y, Yuan F, Wang A, Wang C, Lin L, Wang S, Wang C, Luo X, Xu Q, Yin R, Cheng H, Zhang Y, Sun X, Xi J, Yan J, Zeng F, Chen Y
Induced pluripotent stem cells (SHCDNi002-A cells) isolated from the peripheral blood mononuclear cells of a 1-year-old Chinese girl with mediator complex subunit 12-related syndrome
Wang Y et al. Induced pluripotent stem cells (SHCDNi002-A cells) isolated from the peripheral blood mononuclear cells of a 1-year-old Chinese girl with mediator complex subunit 12-related syndrome. . 2020-07-00. Pubmed ID: 32505899; DOI: 10.1016/j.scr.2020.101838 SHCDNi002-A 2020-07-00 2020-07-00 PubMed: 32505899 DOI: 10.1016/j.scr.2020.101838Associated cell lines:
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Wei L, Zhang J, Chen D, Feng L, Wu C, Wang R, Li X
Generation of an integration-free induced pluripotent stem cell (iPSC) line (ZZUNEUi002-A) from a patient with spinocerebellar ataxia type 3
Wei L et al. Generation of an integration-free induced pluripotent stem cell (iPSC) line (ZZUNEUi002-A) from a patient with spinocerebellar ataxia type 3. . 2020-06-29. Pubmed ID: 32650241; DOI: 10.1016/j.scr.2020.101898 ZZUNEUi002-A 2020-06-29 2020-06-29 PubMed: 32650241 DOI: 10.1016/j.scr.2020.101898Associated cell lines:
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Perepelina K, Kostina A, Klauzen P, Khudiakov A, Rabino M, Crasto S, Zlotina A, Fomicheva Y, Sergushichev A, Oganesian M, Dmitriev A, Kostareva A, Di Pasquale E, Malashicheva A
Generation of two iPSC lines (FAMRCi007-A and FAMRCi007-B) from patient with Emery-Dreifuss muscular dystrophy and heart rhythm abnormalities carrying genetic variant LMNA p.Arg249Gln
Perepelina K et al. Generation of two iPSC lines (FAMRCi007-A and FAMRCi007-B) from patient with Emery-Dreifuss muscular dystrophy and heart rhythm abnormalities carrying genetic variant LMNA p.Arg249Gln. . 2020-06-29. Pubmed ID: 32659731; DOI: 10.1016/j.scr.2020.101895 FAMRCi007-AFAMRCi007-B 2020-06-29 2020-06-29 PubMed: 32659731 DOI: 10.1016/j.scr.2020.101895Associated cell lines:
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Boerstler T, Wend H, Krumbiegel M, Kavyanifar A, Reis A, Lie DC, Winner B, Turan S
CRISPR/Cas9 mediated generation of human ARID1B heterozygous knockout hESC lines to model Coffin-Siris syndrome
Boerstler T et al. CRISPR/Cas9 mediated generation of human ARID1B heterozygous knockout hESC lines to model Coffin-Siris syndrome. . 2020-06-29. Pubmed ID: 32682288; DOI: 10.1016/j.scr.2020.101889 HVRDe006-A-1HVRDe006-A-4HVRDe006-A-6HVRDe006-A-7 2020-06-29 2020-06-29 PubMed: 32682288 DOI: 10.1016/j.scr.2020.101889Associated cell lines:
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Leventoux N, Morimoto S, Hara K, Nakamura S, Ozawa F, Mitsuzawa S, Akiyama T, Nishiyama A, Suzuki N, Warita H, Aoki M, Okano H
Generation of an ALS human iPSC line KEIOi001-A from peripheral blood of a Charcot disease-affected patient carrying TARDBP p.N345K heterozygous SNP mutation
Leventoux N et al. Generation of an ALS human iPSC line KEIOi001-A from peripheral blood of a Charcot disease-affected patient carrying TARDBP p.N345K heterozygous SNP mutation. . 2020-06-28. Pubmed ID: 32659732; DOI: 10.1016/j.scr.2020.101896 KEIOi001-A 2020-06-28 2020-06-28 PubMed: 32659732 DOI: 10.1016/j.scr.2020.101896Associated cell lines:
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Faye Pierre-Antoine, Vedrenne Nicolas, Miressi Federica, Rassat Marion, Romanenko Sergii, Richard Laurence, Bourthoumieu Sylvie, Funalot Benoît, Sturtz Franck, Favreau Frederic, Lia Anne-Sophie
Optimized Protocol to Generate Spinal Motor Neuron Cells from Induced Pluripotent Stem Cells from Charcot Marie Tooth Patients
Faye Pierre-Antoine et al. Optimized Protocol to Generate Spinal Motor Neuron Cells from Induced Pluripotent Stem Cells from Charcot Marie Tooth Patients. . 2020-06-27. DOI: 10.3390/brainsci10070407 LIMFRi001-A 2020-06-27 2020-06-27 DOI: 10.3390/brainsci10070407Associated cell lines:
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De Masi C, Spitalieri P, Murdocca M, Novelli G, Sangiuolo F
Application of CRISPR/Cas9 to human-induced pluripotent stem cells: from gene editing to drug discovery
De Masi C et al. Application of CRISPR/Cas9 to human-induced pluripotent stem cells: from gene editing to drug discovery. . 2020-06-26. Pubmed ID: 32591003; DOI: 10.1186/s40246-020-00276-2; PMC: PMC7318728 IRFMNi003-AIRFMNi003-A-1IRFMNi003-A-2 2020-06-26 2020-06-26 PubMed: 32591003 DOI: 10.1186/s40246-020-00276-2Associated cell lines:
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Liu D, Cheng F, Pan S, Liu Z
Stem cells: a potential treatment option for kidney diseases
Liu D et al. Stem cells: a potential treatment option for kidney diseases. . 2020-06-25. Pubmed ID: 32586408; DOI: 10.1186/s13287-020-01751-2; PMC: PMC7318741 MUSIi005-AIRFMNi003-AIRFMNi003-A-1IRFMNi003-A-2 2020-06-25 2020-06-25 PubMed: 32586408 DOI: 10.1186/s13287-020-01751-2Associated cell lines:
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Ababneh NA, Al-Kurdi B, Ali D, Abuarqoub D, Barham R, Salah B, Awidi A
Establishment of a human induced pluripotent stem cell (iPSC) line (JUCTCi010-A) from a healthy Jordanian female skin dermal fibroblasts
Ababneh NA et al. Establishment of a human induced pluripotent stem cell (iPSC) line (JUCTCi010-A) from a healthy Jordanian female skin dermal fibroblasts. . 2020-06-24. Pubmed ID: 32622344; DOI: 10.1016/j.scr.2020.101891 JUCTCi010-A 2020-06-24 2020-06-24 PubMed: 32622344 DOI: 10.1016/j.scr.2020.101891Associated cell lines:
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Sasaki-Honda M, Kagita A, Jonouchi T, Araki T, Hotta A, Sakurai H
Generation of a transgene-free iPSC line and genetically modified line from a facioscapulohumeral muscular dystrophy type 2 (FSHD2) patient with SMCHD1 p.Lys607Ter mutation
Sasaki-Honda M et al. Generation of a transgene-free iPSC line and genetically modified line from a facioscapulohumeral muscular dystrophy type 2 (FSHD2) patient with SMCHD1 p.Lys607Ter mutation. . 2020-06-24. Pubmed ID: 32711388; DOI: 10.1016/j.scr.2020.101884 CIRAi006-ACIRAi006-A-1 2020-06-24 2020-06-24 PubMed: 32711388 DOI: 10.1016/j.scr.2020.101884Associated cell lines:
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Shan Y, Ma L, Zhang C, Zhang Y, Zhang J, Xiao L, Wei Y, Yu Y
Generation of two RNF2 homozygous knockout human embryonic stem cell lines by CRISPR/Cas9 system
Shan Y et al. Generation of two RNF2 homozygous knockout human embryonic stem cell lines by CRISPR/Cas9 system. . 2020-06-24. Pubmed ID: 32610219; DOI: 10.1016/j.scr.2020.101885 WAe001-A-41WAe001-A-42 2020-06-24 2020-06-24 PubMed: 32610219 DOI: 10.1016/j.scr.2020.101885Associated cell lines:
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Guo X, Wang L, Chen K, Song S, Wang X, Gu X, Niu C, Chu M
Generation of urine-derived iPS cell line via a non-integrative method from a Barth syndrome patient with TAZ gene mutation
Guo X et al. Generation of urine-derived iPS cell line via a non-integrative method from a Barth syndrome patient with TAZ gene mutation. . 2020-06-24. Pubmed ID: 32619718; DOI: 10.1016/j.scr.2020.101886 WMUi002-A 2020-06-24 2020-06-24 PubMed: 32619718 DOI: 10.1016/j.scr.2020.101886Associated cell lines:
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Li X, Lu Y, Wang J, Liu M, Wang M, Hu L, Du W, Wang L, Jiang Z, Gu X, Ding Z, Feng D, Li L, Dong J, Zhao X
An integration-free iPSC line ZZUNEUi008-A derived from dermal fibroblasts of a child with cardiac valvular dysplasia carrying a mutation in FLNA gene
Li X et al. An integration-free iPSC line ZZUNEUi008-A derived from dermal fibroblasts of a child with cardiac valvular dysplasia carrying a mutation in FLNA gene. . 2020-06-22. Pubmed ID: 32592953; DOI: 10.1016/j.scr.2020.101882 ZZUNEUi008-A 2020-06-22 2020-06-22 PubMed: 32592953 DOI: 10.1016/j.scr.2020.101882Associated cell lines:
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Romano E, Trionfini P, Ciampi O, Benigni A, Tomasoni S
Generation of PKD1 mono-allelic and bi-allelic knockout iPS cell lines using CRISPR-Cas9 system
Romano E et al. Generation of PKD1 mono-allelic and bi-allelic knockout iPS cell lines using CRISPR-Cas9 system. . 2020-06-19. Pubmed ID: 32592954; DOI: 10.1016/j.scr.2020.101881 IRFMNi003-A-3IRFMNi003-A-4IRFMNi001-BIRFMNi001-B-1 2020-06-19 2020-06-19 PubMed: 32592954 DOI: 10.1016/j.scr.2020.101881Associated cell lines:
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Sanjurjo-Soriano C, Erkilic N, Baux D, Mamaeva D, Hamel CP, Meunier I, Roux AF, Kalatzis V
Genome Editing in Patient iPSCs Corrects the Most Prevalent USH2A Mutations and Reveals Intriguing Mutant mRNA Expression Profiles
Sanjurjo-Soriano C et al. Genome Editing in Patient iPSCs Corrects the Most Prevalent USH2A Mutations and Reveals Intriguing Mutant mRNA Expression Profiles. . 2020-06-12. Pubmed ID: 31909088; DOI: 10.1016/j.omtm.2019.11.016; PMC: PMC6938853 INMi001-AINMi002-A 2020-06-12 2020-06-12 PubMed: 31909088 DOI: 10.1016/j.omtm.2019.11.016 -
Fleischer A, Vallejo-Díez S, Martín-Fernández JM, Sánchez-Gilabert A, Castresana M, Del Pozo A, Esquisabel A, Ávila S, Castrillo JL, Gaínza E, Pedraz JL, Viñas M, Bachiller D
iPSC-Derived Intestinal Organoids from Cystic Fibrosis Patients Acquire CFTR Activity upon TALEN-Mediated Repair of the p.F508del Mutation
Fleischer A et al. iPSC-Derived Intestinal Organoids from Cystic Fibrosis Patients Acquire CFTR Activity upon TALEN-Mediated Repair of the p.F508del Mutation. . 2020-06-12. Pubmed ID: 32373648; DOI: 10.1016/j.omtm.2020.04.005; PMC: PMC7195499 IMEDEAi001-FIMEDEAi001-F-1 2020-06-12 2020-06-12 PubMed: 32373648 DOI: 10.1016/j.omtm.2020.04.005Associated cell lines:
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Cai Y, Lin J, Ma K, He M, Li B
Generation of a human induced pluripotent stem cell line (SHUPLi001-A) from PBMCs of a healthy male donor
Cai Y et al. Generation of a human induced pluripotent stem cell line (SHUPLi001-A) from PBMCs of a healthy male donor. . 2020-06-10. Pubmed ID: 32592952; DOI: 10.1016/j.scr.2020.101871 SHUPLi001-A 2020-06-10 2020-06-10 PubMed: 32592952 DOI: 10.1016/j.scr.2020.101871Associated cell lines:
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Grubman A, Vandekolk TH, Schröder J, Sun G, Hatwell-Humble J, Chan J, Oksanen M, Lehtonen S, Hunt C, Koistinaho JE, Nilsson SK, Haynes JM, Pouton CW, Polo JM
A CX3CR1 Reporter hESC Line Facilitates Integrative Analysis of In-Vitro-Derived Microglia and Improved Microglia Identity upon Neuron-Glia Co-culture
Grubman A et al. A CX3CR1 Reporter hESC Line Facilitates Integrative Analysis of In-Vitro-Derived Microglia and Improved Microglia Identity upon Neuron-Glia Co-culture. . 2020-06-09. Pubmed ID: 32442534; DOI: 10.1016/j.stemcr.2020.04.007; PMC: PMC7355140 WAe009-AWAe009-A-24 2020-06-09 2020-06-09 PubMed: 32442534 DOI: 10.1016/j.stemcr.2020.04.007Associated cell lines:
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Halliwell JA, Frith TJR, Laing O, Price CJ, Bower OJ, Stavish D, Gokhale PJ, Hewitt Z, El-Khamisy SF, Barbaric I, Andrews PW
Nucleosides Rescue Replication-Mediated Genome Instability of Human Pluripotent Stem Cells
Halliwell JA et al. Nucleosides Rescue Replication-Mediated Genome Instability of Human Pluripotent Stem Cells. . 2020-06-09. Pubmed ID: 32413278; DOI: 10.1016/j.stemcr.2020.04.004; PMC: PMC7355123 UOSi001-AUOSe015-ARUCDRi002-A 2020-06-09 2020-06-09 PubMed: 32413278 DOI: 10.1016/j.stemcr.2020.04.004Associated cell lines:
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Giacomelli E, Meraviglia V, Campostrini G, Cochrane A, Cao X, van Helden RWJ, Krotenberg Garcia A, Mircea M, Kostidis S, Davis RP, van Meer BJ, Jost CR, Koster AJ, Mei H, Míguez DG, Mulder AA, Ledesma-Terrón M, Pompilio G, Sala L, Salvatori DCF, Slieker RC, Sommariva E, de Vries AAF, Giera M, Semrau S, Tertoolen LGJ, Orlova VV, Bellin M, Mummery CL
Human-iPSC-Derived Cardiac Stromal Cells Enhance Maturation in 3D Cardiac Microtissues and Reveal Non-cardiomyocyte Contributions to Heart Disease
Giacomelli E et al. Human-iPSC-Derived Cardiac Stromal Cells Enhance Maturation in 3D Cardiac Microtissues and Reveal Non-cardiomyocyte Contributions to Heart Disease. . 2020-06-04. Pubmed ID: 32459996; DOI: 10.1016/j.stem.2020.05.004; PMC: PMC7284308 LUMCi004-ALUMCi028-A 2020-06-04 2020-06-04 PubMed: 32459996 DOI: 10.1016/j.stem.2020.05.004Associated cell lines:
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Cascalho A, Foroozandeh J, Hennebel L, Swerts J, Klein C, Rous S, Dominguez Gonzalez B, Pisani A, Meringolo M, Gallego SF, Verstreken P, Seibler P, Goodchild RE
Excess Lipin enzyme activity contributes to TOR1A recessive disease and DYT-TOR1A dystonia
Cascalho A et al. Excess Lipin enzyme activity contributes to TOR1A recessive disease and DYT-TOR1A dystonia. . 2020-06-01. Pubmed ID: 32516804; DOI: 10.1093/brain/awaa139 STBCi033-BSTBCi039-ALUEi020-A 2020-06-01 2020-06-01 PubMed: 32516804 DOI: 10.1093/brain/awaa139Associated cell lines:
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Pejskova P, Reilly ML, Bino L, Bernatik O, Dolanska L, Ganji RS, Zdrahal Z, Benmerah A, Cajanek L
KIF14 controls ciliogenesis via regulation of Aurora A and is important for Hedgehog signaling
Pejskova P et al. KIF14 controls ciliogenesis via regulation of Aurora A and is important for Hedgehog signaling. . 2020-06-01. Pubmed ID: 32348467; DOI: 10.1083/jcb.201904107; PMC: PMC7265313 MUNIe007-A 2020-06-01 2020-06-01 PubMed: 32348467 DOI: 10.1083/jcb.201904107Associated cell lines:
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Liu WS, Wang RR, Li WY, Rong M, Liu CL, Ma Y, Wang RL
Investigating the reason for loss-of-function of Src homology 2 domain-containing protein tyrosine phosphatase 2 (SHP2) caused by Y279C mutation through molecular dynamics simulation
Liu WS et al. Investigating the reason for loss-of-function of Src homology 2 domain-containing protein tyrosine phosphatase 2 (SHP2) caused by Y279C mutation through molecular dynamics simulation. . 2020-06-00. Pubmed ID: 31258001; DOI: 10.1080/07391102.2019.1634641 TRNDi003-A 2020-06-00 2020-06-00 PubMed: 31258001 DOI: 10.1080/07391102.2019.1634641Associated cell lines:
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Hassoun D., Djukanovic R., Bedel A., de Vos J.
Les révolutions technologiques : de la prédiction au ciblage thérapeutique
Hassoun D. et al. Les révolutions technologiques : de la prédiction au ciblage thérapeutique. . 2020-06-00. DOI: 10.1016/s1877-1203(20)30016-1 UHOMi001-A 2020-06-00 2020-06-00 DOI: 10.1016/s1877-1203(20)30016-1Associated cell lines:
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Wang X, Wei C, Zhang Z, Liu D, Guo Y, Sun G, Wang Y, Li H, Tian Y, Kang X, Han R, Li Z
Association of growth traits with a structural variation downstream of the KCNJ11 gene: a large population-based study in chickens
Wang X et al. Association of growth traits with a structural variation downstream of the KCNJ11 gene: a large population-based study in chickens. . 2020-06-00. Pubmed ID: 32008360; DOI: 10.1080/00071668.2020.1724878 WAe001-AWAe001-A-12 2020-06-00 2020-06-00 PubMed: 32008360 DOI: 10.1080/00071668.2020.1724878Associated cell lines:
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Comella-Bolla A, Orlandi JG, Miguez A, Straccia M, García-Bravo M, Bombau G, Galofré M, Sanders P, Carrere J, Segovia JC, Blasi J, Allen ND, Alberch J, Soriano J, Canals JM
Human Pluripotent Stem Cell-Derived Neurons Are Functionally Mature In Vitro and Integrate into the Mouse Striatum Following Transplantation
Comella-Bolla A et al. Human Pluripotent Stem Cell-Derived Neurons Are Functionally Mature In Vitro and Integrate into the Mouse Striatum Following Transplantation. . 2020-06-00. Pubmed ID: 32356172; DOI: 10.1007/s12035-020-01907-4; PMC: PMC7253531 GENEAe020-A 2020-06-00 2020-06-00 PubMed: 32356172 DOI: 10.1007/s12035-020-01907-4Associated cell lines:
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Heck AM, Russo J, Wilusz J, Nishimura EO, Wilusz CJ
YTHDF2 destabilizes m(6)A-modified neural-specific RNAs to restrain differentiation in induced pluripotent stem cells
Heck AM et al. YTHDF2 destabilizes m(6)A-modified neural-specific RNAs to restrain differentiation in induced pluripotent stem cells. . 2020-06-00. Pubmed ID: 32169943; DOI: 10.1261/rna.073502.119; PMC: PMC7266156 ICGi007-A 2020-06-00 2020-06-00 PubMed: 32169943 DOI: 10.1261/rna.073502.119Associated cell lines:
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Varderidou-Minasian S, Hinz L, Hagemans D, Posthuma D, Altelaar M, Heine VM
Quantitative proteomic analysis of Rett iPSC-derived neuronal progenitors
Varderidou-Minasian S et al. Quantitative proteomic analysis of Rett iPSC-derived neuronal progenitors. . 2020-05-27. Pubmed ID: 32460858; DOI: 10.1186/s13229-020-00344-3; PMC: PMC7251722 TRNDi001-D 2020-05-27 2020-05-27 PubMed: 32460858 DOI: 10.1186/s13229-020-00344-3Associated cell lines:
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Tiklová K, Nolbrant S, Fiorenzano A, Björklund ÅK, Sharma Y, Heuer A, Gillberg L, Hoban DB, Cardoso T, Adler AF, Birtele M, Lundén-Miguel H, Volakakis N, Kirkeby A, Perlmann T, Parmar M
Single cell transcriptomics identifies stem cell-derived graft composition in a model of Parkinson's disease
Tiklová K et al. Single cell transcriptomics identifies stem cell-derived graft composition in a model of Parkinson's disease. . 2020-05-15. Pubmed ID: 32415072; DOI: 10.1038/s41467-020-16225-5; PMC: PMC7229159 WAe009-ARCe021-AKIe033-A 2020-05-15 2020-05-15 PubMed: 32415072 DOI: 10.1038/s41467-020-16225-5 -
Ścieżyńska A, Soszyńska M, Komorowski M, Podgórska A, Krześniak N, Nogowska A, Smolińska M, Szulborski K, Szaflik JP, Noszczyk B, Ołdak M, Malejczyk J
Molecular Analysis of the ABCA4 Gene Mutations in Patients with Stargardt Disease Using Human Hair Follicles
Ścieżyńska A et al. Molecular Analysis of the ABCA4 Gene Mutations in Patients with Stargardt Disease Using Human Hair Follicles. . 2020-05-13. Pubmed ID: 32413971; DOI: 10.3390/ijms21103430; PMC: PMC7279462 FRIMOi003-AFRIMOi004-A 2020-05-13 2020-05-13 PubMed: 32413971 DOI: 10.3390/ijms21103430Associated cell lines:
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Lee H, Flynn R, Sharma I, Haberman E, Carling PJ, Nicholls FJ, Stegmann M, Vowles J, Haenseler W, Wade-Martins R, James WS, Cowley SA
LRRK2 Is Recruited to Phagosomes and Co-recruits RAB8 and RAB10 in Human Pluripotent Stem Cell-Derived Macrophages
Lee H et al. LRRK2 Is Recruited to Phagosomes and Co-recruits RAB8 and RAB10 in Human Pluripotent Stem Cell-Derived Macrophages. . 2020-05-12. Pubmed ID: 32359446; DOI: 10.1016/j.stemcr.2020.04.001; PMC: PMC7221108 STBCi026-ASTBCi044-ASTBCi063-ASTBCi064-ASTBCi066-ASTBCi004-BSTBCi004-B-1STBCi026-A-1STBCi026-A-2STBCi321-A 2020-05-12 2020-05-12 PubMed: 32359446 DOI: 10.1016/j.stemcr.2020.04.001Associated cell lines:
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Martin-Fernandez M, Bravo García-Morato M, Gruber C, Murias Loza S, Malik MNH, Alsohime F, Alakeel A, Valdez R, Buta S, Buda G, Marti MA, Larralde M, Boisson B, Feito Rodriguez M, Qiu X, Chrabieh M, Al Ayed M, Al Muhsen S, Desai JV, Ferre EMN, Rosenzweig SD, Amador-Borrero B, Bravo-Gallego LY, Olmer R, Merkert S, Bret M, Sood AK, Al-Rabiaah A, Temsah MH, Halwani R, Hernandez M, Pessler F, Casanova JL, Bustamante J, Lionakis MS, Bogunovic D
Systemic Type I IFN Inflammation in Human ISG15 Deficiency Leads to Necrotizing Skin Lesions
Martin-Fernandez M et al. Systemic Type I IFN Inflammation in Human ISG15 Deficiency Leads to Necrotizing Skin Lesions. . 2020-05-12. Pubmed ID: 32402279; DOI: 10.1016/j.celrep.2020.107633; PMC: PMC7331931 MHHi001-A 2020-05-12 2020-05-12 PubMed: 32402279 DOI: 10.1016/j.celrep.2020.107633Associated cell lines:
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Sürün D, Schneider A, Mircetic J, Neumann K, Lansing F, Paszkowski-Rogacz M, Hänchen V, Lee-Kirsch MA, Buchholz F
Efficient Generation and Correction of Mutations in Human iPS Cells Utilizing mRNAs of CRISPR Base Editors and Prime Editors
Sürün D et al. Efficient Generation and Correction of Mutations in Human iPS Cells Utilizing mRNAs of CRISPR Base Editors and Prime Editors. . 2020-05-06. Pubmed ID: 32384610; DOI: 10.3390/genes11050511; PMC: PMC7288465 BIHi001-ABIHi001-A-2CRTDi003-ACRTDi003-B 2020-05-06 2020-05-06 PubMed: 32384610 DOI: 10.3390/genes11050511Associated cell lines:
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Gatinois V, Desprat R, Pichard L, Becker F, Goldenberg A, Balguerie X, Pellestor F, Lemaitre JM
iPSC reprogramming of fibroblasts from a patient with a Rothmund-Thomson syndrome RTS
Gatinois V et al. iPSC reprogramming of fibroblasts from a patient with a Rothmund-Thomson syndrome RTS. . 2020-05-00. Pubmed ID: 32416578; DOI: 10.1016/j.scr.2020.101807 REGUi003-AREGUi005-A 2020-05-00 2020-05-00 PubMed: 32416578 DOI: 10.1016/j.scr.2020.101807Associated cell lines:
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Yan Y, Qiu Y, Zhao A, Zhao J, Wang Y, Deng Y
Establishment of SIAISi002-A, an induced pluripotent stem cell (iPSC) line from 39-year old healthy female donor with a family history of Alzheimer's disease (AD) and two copies of APOE4 gene
Yan Y et al. Establishment of SIAISi002-A, an induced pluripotent stem cell (iPSC) line from 39-year old healthy female donor with a family history of Alzheimer's disease (AD) and two copies of APOE4 gene. . 2020-05-00. Pubmed ID: 32339902; DOI: 10.1016/j.scr.2020.101792 SIAISi002-A 2020-05-00 2020-05-00 PubMed: 32339902 DOI: 10.1016/j.scr.2020.101792Associated cell lines:
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Kamata K, Otsuka Y, Imamura K, Oishi A, Kondo T, Suga M, Shibukawa R, Okanishi Y, Sagara Y, Tsukita K, Yasukawa T, Usui H, Muguruma K, Tsujikawa A, Inoue H
Generation of a human induced pluripotent stem cell line, BRCi005-A, derived from a Best disease patient with BEST1 mutations
Kamata K et al. Generation of a human induced pluripotent stem cell line, BRCi005-A, derived from a Best disease patient with BEST1 mutations. . 2020-05-00. Pubmed ID: 32416576; DOI: 10.1016/j.scr.2020.101782 BRCi005-A 2020-05-00 2020-05-00 PubMed: 32416576 DOI: 10.1016/j.scr.2020.101782Associated cell lines:
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Sun C, Zhou P, Yuan S, Guo R, Zhang Z, Xu Q, Han D, He L, Tang H, Xu K, Hu H, Li N
Generation of an induced pluripotent stem cell line SYSUi-004-A from a child of microcephaly with TYW1 mutations
Sun C et al. Generation of an induced pluripotent stem cell line SYSUi-004-A from a child of microcephaly with TYW1 mutations. . 2020-05-00. Pubmed ID: 32279010; DOI: 10.1016/j.scr.2020.101783 SYSUi004-A 2020-05-00 2020-05-00 PubMed: 32279010 DOI: 10.1016/j.scr.2020.101783Associated cell lines:
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Blöchinger AK, Siehler J, Wißmiller K, Shahryari A, Burtscher I, Lickert H
Generation of an INSULIN-H2B-Cherry reporter human iPSC line
Blöchinger AK et al. Generation of an INSULIN-H2B-Cherry reporter human iPSC line. . 2020-05-00. Pubmed ID: 32361463; DOI: 10.1016/j.scr.2020.101797 HMGUi001-AHMGUi001-A-1 2020-05-00 2020-05-00 PubMed: 32361463 DOI: 10.1016/j.scr.2020.101797Associated cell lines:
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Chen G, Li Z, Liu Y, Chen D, Beers J, Cudrici C, Ferrante EA, Schwartzbeck R, Dmitrieva N, Yang D, Zou J, Iruela-Arispe ML, Boehm M
Generation of human induced pluripotent stem cells (NIHTVBi004-A, NIHTVBi005-A, NIHTVBi006-A, NIHTVBi007-A, NIHTVBi008-A) from 5 CADASIL patients with NOTCH3 mutation
Chen G et al. Generation of human induced pluripotent stem cells (NIHTVBi004-A, NIHTVBi005-A, NIHTVBi006-A, NIHTVBi007-A, NIHTVBi008-A) from 5 CADASIL patients with NOTCH3 mutation. . 2020-05-00. Pubmed ID: 32344328; DOI: 10.1016/j.scr.2020.101821; PMC: PMC7309701 NIHTVBi004-ANIHTVBi005-ANIHTVBi006-ANIHTVBi007-ANIHTVBi008-A 2020-05-00 2020-05-00 PubMed: 32344328 DOI: 10.1016/j.scr.2020.101821Associated cell lines:
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Zhang J, Wei L, Wang R, Li X, Liu Z
Generation of an integration-free induced pluripotent stem cell (iPSC) line (ZZUNEUi001-A) from a healthy male individual
Zhang J et al. Generation of an integration-free induced pluripotent stem cell (iPSC) line (ZZUNEUi001-A) from a healthy male individual. . 2020-05-00. Pubmed ID: 32361313; DOI: 10.1016/j.scr.2020.101809 SYSUi001-AZZUNEUi001-AZZUNEUi003-A 2020-05-00 2020-05-00 PubMed: 32361313 DOI: 10.1016/j.scr.2020.101809Associated cell lines:
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Long P, Liu Z, Wu B, Chen J, Sun C, Wang F, Huang Y, Chen H, Li Q, Ma Y
Generation of an induced pluripotent stem cell line from chorionic villi of a Patau syndrome spontaneous abortion
Long P et al. Generation of an induced pluripotent stem cell line from chorionic villi of a Patau syndrome spontaneous abortion. . 2020-05-00. Pubmed ID: 32361311; DOI: 10.1016/j.scr.2020.101789 HNMUi001-A 2020-05-00 2020-05-00 PubMed: 32361311 DOI: 10.1016/j.scr.2020.101789Associated cell lines:
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Yuan F, Wang C, Xi J, Wang S, Lin L, Wang Y, Wang A, Wang C, Luo X, Xu Q, Yin R, Cheng H, Zhang Y, Sun X, Chen Y
Generation of an induced pluripotent stem cell line SHCDNi001-A from a one-year-old Chinese girl with mitochondrial DNA depletion syndrome 13
Yuan F et al. Generation of an induced pluripotent stem cell line SHCDNi001-A from a one-year-old Chinese girl with mitochondrial DNA depletion syndrome 13. . 2020-05-00. Pubmed ID: 32416579; DOI: 10.1016/j.scr.2020.101832 SHCDNi001-A 2020-05-00 2020-05-00 PubMed: 32416579 DOI: 10.1016/j.scr.2020.101832Associated cell lines:
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Larsen SB, Hanss Z, Cruciani G, Massart F, Barbuti PA, Mellick G, Krüger R
Induced pluripotent stem cell line (LCSBi001-A) derived from a patient with Parkinson's disease carrying the p.D620N mutation in VPS35
Larsen SB et al. Induced pluripotent stem cell line (LCSBi001-A) derived from a patient with Parkinson's disease carrying the p.D620N mutation in VPS35. . 2020-05-00. Pubmed ID: 32387898; DOI: 10.1016/j.scr.2020.101776 LCSBi001-A 2020-05-00 2020-05-00 PubMed: 32387898 DOI: 10.1016/j.scr.2020.101776Associated cell lines:
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Zhou Y, Jing Y, Mao S, Liu J, Cui Z, Wang Y, Chen J, Chan HF, Tang S, Chen J
Establishment of induced pluripotent stem cell line CSUASOi004-A by reprogramming peripheral blood mononuclear cells of a PRPF6-related dominant retinitis pigmentosa patient
Zhou Y et al. Establishment of induced pluripotent stem cell line CSUASOi004-A by reprogramming peripheral blood mononuclear cells of a PRPF6-related dominant retinitis pigmentosa patient. . 2020-05-00. Pubmed ID: 32335390; DOI: 10.1016/j.scr.2020.101793 CSUASOi004-A 2020-05-00 2020-05-00 PubMed: 32335390 DOI: 10.1016/j.scr.2020.101793Associated cell lines:
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Sun L, Zhang J, Kuang XY, Kang YL, Wu Y, Huang WY
Generation of an induced pluripotent stem cell line (SHCDNRi001-A) from a patient with X-linked Alport syndrome carrying a heterozygous p.G409S (c. 1225 G > A) mutation in the COL4A5 gene
Sun L et al. Generation of an induced pluripotent stem cell line (SHCDNRi001-A) from a patient with X-linked Alport syndrome carrying a heterozygous p.G409S (c. 1225 G > A) mutation in the COL4A5 gene. . 2020-05-00. Pubmed ID: 32416580; DOI: 10.1016/j.scr.2020.101833 SHCDNRi001-A 2020-05-00 2020-05-00 PubMed: 32416580 DOI: 10.1016/j.scr.2020.101833Associated cell lines:
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Duarte AJ, Ribeiro D, Santos R, Moreira L, Bragança J, Amaral O
Induced pluripotent stem cell line (INSAi002-A) from a Fabry Disease patient hemizygote for the rare p.W287X mutation
Duarte AJ et al. Induced pluripotent stem cell line (INSAi002-A) from a Fabry Disease patient hemizygote for the rare p.W287X mutation. . 2020-05-00. Pubmed ID: 32388441; DOI: 10.1016/j.scr.2020.101794; PMC: https://www.sciencedirect.com/science/article/pii/S1873506120300970?via%3Dihub INSAi002-A 2020-05-00 2020-05-00 PubMed: 32388441 DOI: 10.1016/j.scr.2020.101794Associated cell lines:
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Zhang L, Ren Q, Liu G, Wu R, Meng S, Xiahou K, Jiang N, Zhang Y, Zhou W
Establishment of two induced pluripotent stem cell line from healthy elderly (IPTi005-A and IPTi007-A)
Zhang L et al. Establishment of two induced pluripotent stem cell line from healthy elderly (IPTi005-A and IPTi007-A). . 2020-05-00. Pubmed ID: 32402716; DOI: 10.1016/j.scr.2020.101808 IPTi005-AIPTi007-A 2020-05-00 2020-05-00 PubMed: 32402716 DOI: 10.1016/j.scr.2020.101808 -
Huang CY, Tsai YH, Tsai YC, Lu YC, Chan YH, Hsu CJ, Chiou SH, Wu CC, Cheng YF
Establishment of an induced pluripotent stem cell (iPSC) line from a 7-year-old male patient with profound hearing loss carrying c.235delC in GJB2 gene
Huang CY et al. Establishment of an induced pluripotent stem cell (iPSC) line from a 7-year-old male patient with profound hearing loss carrying c.235delC in GJB2 gene. . 2020-05-00. Pubmed ID: 32388442; DOI: 10.1016/j.scr.2020.101795 TVGHi007-A 2020-05-00 2020-05-00 PubMed: 32388442 DOI: 10.1016/j.scr.2020.101795Associated cell lines:
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Chen M, Maimaitili M, Buchholdt SH, Jensen UB, Febbraro F, Denham M
Generation of an induced pluripotent stem cell line (DANi-011A) from a Parkinson's disease patient with a LRRK2 p.G2019S mutation
Chen M et al. Generation of an induced pluripotent stem cell line (DANi-011A) from a Parkinson's disease patient with a LRRK2 p.G2019S mutation. . 2020-05-00. Pubmed ID: 32305865; DOI: 10.1016/j.scr.2020.101781 DANi011-A 2020-05-00 2020-05-00 PubMed: 32305865 DOI: 10.1016/j.scr.2020.101781Associated cell lines:
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Lilianty J, Nur Patria Y, Stanley EG, Elefanty AG, Bateman JF, Lamandé SR
Generation of a heterozygous COL2A1 (p.R989C) spondyloepiphyseal dysplasia congenita mutation iPSC line, MCRIi001-B, using CRISPR/Cas9 gene editing
Lilianty J et al. Generation of a heterozygous COL2A1 (p.R989C) spondyloepiphyseal dysplasia congenita mutation iPSC line, MCRIi001-B, using CRISPR/Cas9 gene editing. . 2020-05-00. Pubmed ID: 32446218; DOI: 10.1016/j.scr.2020.101843 MCRIi001-AMCRIi001-A-2MCRIi001-B 2020-05-00 2020-05-00 PubMed: 32446218 DOI: 10.1016/j.scr.2020.101843Associated cell lines:
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Main H, Hedenskog M, Acharya G, Hovatta O, Lanner F
Karolinska Institutet Human Embryonic Stem Cell Bank
Main H et al. Karolinska Institutet Human Embryonic Stem Cell Bank. . 2020-05-00. Pubmed ID: 32339905; DOI: 10.1016/j.scr.2020.101810 KIe001-AKIe002-AKIe003-AKIe004-AKIe005-AKIe006-AKIe007-AKIe008-AKIe009-AKIe010-AKIe011-AKIe012-AKIe013-AKIe014-AKIe015-AKIe016-AKIe017-AKIe018-AKIe019-AKIe020-AKIe021-AKIe022-AKIe023-AKIe024-AKIe025-AKIe026-AKIe027-AKIe028-AKIe029-AKIe030-AKIe031-AKIe001-A-1KIe032-AKIe033-AKIe034-AKIe035-AKIe036-AKIe037-AKIe038-AKIe039-AKIe040-AKIe041-AKIe042-AKIe043-AKIe044-AKIe045-AKIe046-AKIe047-AKIe048-AKIe049-AKIe050-AKIe051-AKIe052-AKIe053-AKIe054-AKIe055-AKIe056-AKIe057-AKIe058-AKIe059-AKIe060-AKIe061-A 2020-05-00 2020-05-00 PubMed: 32339905 DOI: 10.1016/j.scr.2020.101810 -
Wan R, Zhang Q, Li H, Xu X, Tang S
Generation of an iPSC line (CHWi001-A) from peripheral blood mononuclear cells in a patient with intellectual disability and haploinsufficiency of PLPPR4
Wan R et al. Generation of an iPSC line (CHWi001-A) from peripheral blood mononuclear cells in a patient with intellectual disability and haploinsufficiency of PLPPR4. . 2020-05-00. Pubmed ID: 32388443; DOI: 10.1016/j.scr.2020.101811 PUMCHi001-ACHWi001-A 2020-05-00 2020-05-00 PubMed: 32388443 DOI: 10.1016/j.scr.2020.101811Associated cell lines:
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Chen Z, Peng F, Liu J, Xie B, Xu P, Gan Z, Li M, Xu L, Zhong X
Generation of an iPSC line (SKLOi001-A) from a patient with CLCN2-related leukoencephalopathy
Chen Z et al. Generation of an iPSC line (SKLOi001-A) from a patient with CLCN2-related leukoencephalopathy. . 2020-05-00. Pubmed ID: 32278302; DOI: 10.1016/j.scr.2020.101769 SKLOi001-A 2020-05-00 2020-05-00 PubMed: 32278302 DOI: 10.1016/j.scr.2020.101769Associated cell lines:
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Laidou S, Alanis-Lobato G, Pribyl J, Raskó T, Tichy B, Mikulasek K, Tsagiopoulou M, Oppelt J, Kastrinaki G, Lefaki M, Singh M, Zink A, Chondrogianni N, Psomopoulos F, Prigione A, Ivics Z, Pospisilova S, Skladal P, Izsvák Z, Andrade-Navarro MA, Petrakis S
Nuclear inclusions of pathogenic ataxin-1 induce oxidative stress and perturb the protein synthesis machinery
Laidou S et al. Nuclear inclusions of pathogenic ataxin-1 induce oxidative stress and perturb the protein synthesis machinery. . 2020-05-00. Pubmed ID: 32145456; DOI: 10.1016/j.redox.2020.101458; PMC: PMC7058924 LUMCi002-ALUMCi003-A 2020-05-00 2020-05-00 PubMed: 32145456 DOI: 10.1016/j.redox.2020.101458Associated cell lines:
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Seo HH, Han HW, Kim JH
Generation of a TLR7 heterozygous knockout line (WAe009-A-18) from human embryonic stem cells using CRISPR/Cas9
Seo HH et al. Generation of a TLR7 heterozygous knockout line (WAe009-A-18) from human embryonic stem cells using CRISPR/Cas9. . 2020-05-00. Pubmed ID: 32268246; DOI: 10.1016/j.scr.2020.101735 WAe009-AWAe009-A-18 2020-05-00 2020-05-00 PubMed: 32268246 DOI: 10.1016/j.scr.2020.101735Associated cell lines:
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Liu CL, Huang CY, Chen HC, Lu HE, Hsieh PCH, Lee JJ
Generation of a gene corrected human isogenic IBMS-iPSC-014-C from polycystic-kidney-disease induced pluripotent stem cell line using CRISPR/Cas9
Liu CL et al. Generation of a gene corrected human isogenic IBMS-iPSC-014-C from polycystic-kidney-disease induced pluripotent stem cell line using CRISPR/Cas9. . 2020-05-00. Pubmed ID: 32361310; DOI: 10.1016/j.scr.2020.101784 IBMSi003-A-1 2020-05-00 2020-05-00 PubMed: 32361310 DOI: 10.1016/j.scr.2020.101784Associated cell lines:
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Feng B, Ma J, Amponsah AE, Guo R, Kong D, He J, Jiang Y, Zhang W, Zhang Z, Song Y, Shen S, O'Brien T, Cui H
Induced pluripotent stem cell line derived from a sporadic amyotrophic lateral sclerosis patient
Feng B et al. Induced pluripotent stem cell line derived from a sporadic amyotrophic lateral sclerosis patient. . 2020-05-00. Pubmed ID: 32434130; DOI: 10.1016/j.scr.2020.101841 HEBHMUi004-A 2020-05-00 2020-05-00 PubMed: 32434130 DOI: 10.1016/j.scr.2020.101841Associated cell lines:
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He S, Hu J, Zheng Z, Wang J, Chen J, Zhang C, Li L, Wang J, Chen Z, Shi H, Wang J
Establishment of an induced pluripotent stem cell line from a patient with CHARGE syndrome carrying a CHD7 (p.L1151Gfs*17) mutation
He S et al. Establishment of an induced pluripotent stem cell line from a patient with CHARGE syndrome carrying a CHD7 (p.L1151Gfs*17) mutation. . 2020-05-00. Pubmed ID: 32247258; DOI: 10.1016/j.scr.2020.101774 JTUi001-A 2020-05-00 2020-05-00 PubMed: 32247258 DOI: 10.1016/j.scr.2020.101774Associated cell lines:
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Suzuki H, Egawa N, Kondo T, Imamura K, Enami T, Tsukita K, Suga M, Shibukawa R, Okanishi Y, Uchiyama T, Inoue H, Takahashi R
Generation of a human induced pluripotent stem cell line derived from a Parkinson's disease patient carrying SNCA duplication
Suzuki H et al. Generation of a human induced pluripotent stem cell line derived from a Parkinson's disease patient carrying SNCA duplication. . 2020-05-00. Pubmed ID: 32413791; DOI: 10.1016/j.scr.2020.101828 BRCi008-A 2020-05-00 2020-05-00 PubMed: 32413791 DOI: 10.1016/j.scr.2020.101828Associated cell lines:
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Kamata K, Otsuka Y, Imamura K, Oishi A, Kondo T, Suga M, Shibukawa R, Okanishi Y, Sagara Y, Tsukita K, Yasukawa T, Usui H, Muguruma K, Tsujikawa A, Inoue H
Generation of a human induced pluripotent stem cell line, BRCi004-A, derived from a patient with age-related macular degeneration
Kamata K et al. Generation of a human induced pluripotent stem cell line, BRCi004-A, derived from a patient with age-related macular degeneration. . 2020-05-00. Pubmed ID: 32416577; DOI: 10.1016/j.scr.2020.101787 BRCi004-A 2020-05-00 2020-05-00 PubMed: 32416577 DOI: 10.1016/j.scr.2020.101787Associated cell lines:
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Döpper H, Horstmann M, Menges J, Bozet M, Kanber D, Steenpass L
Biallelic and monoallelic deletion of the RB1 promoter in six isogenic clonal H9 hESC lines
Döpper H et al. Biallelic and monoallelic deletion of the RB1 promoter in six isogenic clonal H9 hESC lines. . 2020-05-00. Pubmed ID: 32268247; DOI: 10.1016/j.scr.2020.101779 WAe009-A-30WAe009-A-31WAe009-A-32WAe009-A-33WAe009-A-34WAe009-A-35 2020-05-00 2020-05-00 PubMed: 32268247 DOI: 10.1016/j.scr.2020.101779Associated cell lines:
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Vaidyanath A, Khan M, Shiras A
Generation of two control iPSC clones NCCSi008-A and NCCSi008-B from an individual of Indian ethnicity
Vaidyanath A et al. Generation of two control iPSC clones NCCSi008-A and NCCSi008-B from an individual of Indian ethnicity. . 2020-05-00. Pubmed ID: 32315960; DOI: 10.1016/j.scr.2020.101765 NCCSi008-ANCCSi008-B 2020-05-00 2020-05-00 PubMed: 32315960 DOI: 10.1016/j.scr.2020.101765Associated cell lines:
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Rovina D, Castiglioni E, Niro F, Farini A, Belicchi M, Di Fede E, Gervasini C, Paganini S, Di Segni M, Torrente Y, Santoro R, Pompilio G, Gowran A
Generation of the Becker muscular dystrophy patient derived induced pluripotent stem cell line carrying the DMD splicing mutation c.1705-8 T>C
Rovina D et al. Generation of the Becker muscular dystrophy patient derived induced pluripotent stem cell line carrying the DMD splicing mutation c.1705-8 T>C. . 2020-05-00. Pubmed ID: 32348941; DOI: 10.1016/j.scr.2020.101819; PMC: PMC7264707 CCMi004-A 2020-05-00 2020-05-00 PubMed: 32348941 DOI: 10.1016/j.scr.2020.101819Associated cell lines:
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He L, Zhao H, Li S, Han X, Chen Z, Wang C, Tian C, Tang F, Huang R, Lin Z, Li Z, Tang B, Jiang H
Generation of induced pluripotent stem cell line (CSUXHi002-A) from a patient with spinocerebellar ataxia type 1
He L et al. Generation of induced pluripotent stem cell line (CSUXHi002-A) from a patient with spinocerebellar ataxia type 1. . 2020-05-00. Pubmed ID: 32335388; DOI: 10.1016/j.scr.2020.101816 CSUXHi001-ACSUXHi002-A 2020-05-00 2020-05-00 PubMed: 32335388 DOI: 10.1016/j.scr.2020.101816Associated cell lines:
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Liu B, Chen L, Sun J, Zhang L, Chen M, Qian Y, Wang Y, Yan K, Hou L, Huang Y, Zhang D, Xu Y, Yu J, Zhang J, Dong M
Generation of the human induced pluripotent stem cell line (ZJUi005-A) from a patient with Pelizaeus-Merzbacher disease (PMD) carrying a novel hemizygous mutation in PLP1 gene
Liu B et al. Generation of the human induced pluripotent stem cell line (ZJUi005-A) from a patient with Pelizaeus-Merzbacher disease (PMD) carrying a novel hemizygous mutation in PLP1 gene. . 2020-05-00. Pubmed ID: 32402715; DOI: 10.1016/j.scr.2020.101791 ZJUi005-A 2020-05-00 2020-05-00 PubMed: 32402715 DOI: 10.1016/j.scr.2020.101791Associated cell lines:
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Tang X, Liu X, Chen Z, Luo L, Liu X, Deng J, Li DW, Liu Y
Using inducible lentiviral vectors to generate induced pluripotent stem cell line ZOCi001-A from peripheral blood cells of a patient with CRB1(-/-) retinitis pigmentosa
Tang X et al. Using inducible lentiviral vectors to generate induced pluripotent stem cell line ZOCi001-A from peripheral blood cells of a patient with CRB1(-/-) retinitis pigmentosa. . 2020-05-00. Pubmed ID: 32387899; DOI: 10.1016/j.scr.2020.101817 ZOCi001-A 2020-05-00 2020-05-00 PubMed: 32387899 DOI: 10.1016/j.scr.2020.101817Associated cell lines:
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Konala VBR, Nandakumar S, Battu R, Pal R
Derivation of three induced pluripotent stem cell lines under feeder-free culture conditions from peripheral blood mononuclear cells (PBMC) of Indian patients suffering from inherited retinal diseases carrying different mutations
Konala VBR et al. Derivation of three induced pluripotent stem cell lines under feeder-free culture conditions from peripheral blood mononuclear cells (PBMC) of Indian patients suffering from inherited retinal diseases carrying different mutations. . 2020-05-00. Pubmed ID: 32278301; DOI: 10.1016/j.scr.2020.101757 ERPLi001-AERPLi002-AERPLi003-A 2020-05-00 2020-05-00 PubMed: 32278301 DOI: 10.1016/j.scr.2020.101757Associated cell lines:
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Sun X, Zhou X, Xiao X, Chi J, Dong B, Wang Y
Generation of the induced pluripotent stem cell(iPSC) line (AHQUi001-A) from a patient with familial hypertriglyceridemia (FHTG) carrying a heterozygous p.C310R (c.928 T > C) mutation in LPL gene
Sun X et al. Generation of the induced pluripotent stem cell(iPSC) line (AHQUi001-A) from a patient with familial hypertriglyceridemia (FHTG) carrying a heterozygous p.C310R (c.928 T > C) mutation in LPL gene. . 2020-05-00. Pubmed ID: 32353702; DOI: 10.1016/j.scr.2020.101802 AHQUi001-A 2020-05-00 2020-05-00 PubMed: 32353702 DOI: 10.1016/j.scr.2020.101802Associated cell lines:
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Raman S, Brookhouser N, Brafman DA
Using human induced pluripotent stem cells (hiPSCs) to investigate the mechanisms by which Apolipoprotein E (APOE) contributes to Alzheimer's disease (AD) risk
Raman S et al. Using human induced pluripotent stem cells (hiPSCs) to investigate the mechanisms by which Apolipoprotein E (APOE) contributes to Alzheimer's disease (AD) risk. . 2020-05-00. Pubmed ID: 32032733; DOI: 10.1016/j.nbd.2020.104788; PMC: PMC7098264 UKBi011-AASUi001-AASUi002-AASUi003-AASUi004-ATUSMi003-AASUi005-AASUi006-A 2020-05-00 2020-05-00 PubMed: 32032733 DOI: 10.1016/j.nbd.2020.104788 -
Tariq M, Liu H, Ibañez DP, Li Y, Chen S, Jiang M, Fan W, Zhao P, Luo Z, Wang D, Kanwal S
Generation of three induced pluripotent stem cell lines from a Parkinson's disease patient with mutant PARKIN (p. C253Y)
Tariq M et al. Generation of three induced pluripotent stem cell lines from a Parkinson's disease patient with mutant PARKIN (p. C253Y). . 2020-05-00. Pubmed ID: 32387897; DOI: 10.1016/j.scr.2020.101822 GIBHi006-AGIBHi006-BGIBHi006-C 2020-05-00 2020-05-00 PubMed: 32387897 DOI: 10.1016/j.scr.2020.101822Associated cell lines:
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Hu J, Ren W, Qiu W, Lv J, Zhang C, Xu C, DU W, Wu M, Wang J, Quan R
Generation of induced pluripotent stem cell line (XDCMHi001-A) from an Ankylosing spondylitis patient with JAK2 mutation
Hu J et al. Generation of induced pluripotent stem cell line (XDCMHi001-A) from an Ankylosing spondylitis patient with JAK2 mutation. . 2020-05-00. Pubmed ID: 32388440; DOI: 10.1016/j.scr.2020.101788 XDCMHi001-A 2020-05-00 2020-05-00 PubMed: 32388440 DOI: 10.1016/j.scr.2020.101788Associated cell lines:
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Zhang Y, Li H, Wang J, Wang G, Tan X, Lei M
Generation of three iPSC lines (XACHi007-A, XACHi008-A, XACHi009-A) from a Chinese family with long QT syndrome type 5 with heterozygous c.226G>A (p.D76N) mutation in KCNE1gene
Zhang Y et al. Generation of three iPSC lines (XACHi007-A, XACHi008-A, XACHi009-A) from a Chinese family with long QT syndrome type 5 with heterozygous c.226G>A (p.D76N) mutation in KCNE1gene. . 2020-05-00. Pubmed ID: 32344329; DOI: 10.1016/j.scr.2020.101798 XACHi007-AXACHi008-AXACHi009-A 2020-05-00 2020-05-00 PubMed: 32344329 DOI: 10.1016/j.scr.2020.101798Associated cell lines:
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Ciolak A, Krzyzosiak WJ, Kozlowska E, Fiszer A
Generation of human iPS cell line IBCHi002-A from spinocerebellar ataxia type 3/Machado-Joseph disease patient's fibroblasts
Ciolak A et al. Generation of human iPS cell line IBCHi002-A from spinocerebellar ataxia type 3/Machado-Joseph disease patient's fibroblasts. . 2020-05-00. Pubmed ID: 32361312; DOI: 10.1016/j.scr.2020.101796 IBCHi001-AIBCHi002-A 2020-05-00 2020-05-00 PubMed: 32361312 DOI: 10.1016/j.scr.2020.101796Associated cell lines:
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Khurana P, Kolundzic N, Rogar M, Hobbs C, Wong XFCC, Common JEA, Ilic D, Liovic M
Stem Cell Research Lab Resource: Stem Cell LineInduced pluripotent stem cell (iPSC) line MLi-003A derived from an individual with the maximum number of filaggrin (FLG) tandem repeats
Khurana P et al. Stem Cell Research Lab Resource: Stem Cell LineInduced pluripotent stem cell (iPSC) line MLi-003A derived from an individual with the maximum number of filaggrin (FLG) tandem repeats. . 2020-05-00. Pubmed ID: 32361315; DOI: 10.1016/j.scr.2020.101827 MLi003-AKCLi003-A 2020-05-00 2020-05-00 PubMed: 32361315 DOI: 10.1016/j.scr.2020.101827 -
Zhao H, Li S, He L, Han X, Huang H, Tang F, Lin Z, Deng S, Tian C, Huang R, Li Z
Generation of iPSC line (USTCi001-A) from human skin fibroblasts of a patient with epilepsy
Zhao H et al. Generation of iPSC line (USTCi001-A) from human skin fibroblasts of a patient with epilepsy. . 2020-05-00. Pubmed ID: 32335389; DOI: 10.1016/j.scr.2020.101785 USTCi001-AUSTCi001-A-2 2020-05-00 2020-05-00 PubMed: 32335389 DOI: 10.1016/j.scr.2020.101785Associated cell lines:
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Ullah H, You H, Shah Z, Fan C, Zhang B, Liu H, Zhang J, Abbas N, Filonenko ES, Samokhvalov IM
Generation of RUNX1-null reporter human embryonic stem cell line GIBHe008-A
Ullah H et al. Generation of RUNX1-null reporter human embryonic stem cell line GIBHe008-A. . 2020-05-00. Pubmed ID: 32371361; DOI: 10.1016/j.scr.2020.101800 WAe001-A-44 2020-05-00 2020-05-00 PubMed: 32371361 DOI: 10.1016/j.scr.2020.101800Associated cell lines:
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Meraviglia V, Arendzen CH, Freund C, Atsma DE, Mummery CL, Bellin M
Generation of two human induced pluripotent stem cell lines, LUMCi020-A and LUMCi021-A, from two patients with Catecholaminergic Polymorphic Ventricular Tachycardia carrying heterozygous mutations in the RYR2 gene
Meraviglia V et al. Generation of two human induced pluripotent stem cell lines, LUMCi020-A and LUMCi021-A, from two patients with Catecholaminergic Polymorphic Ventricular Tachycardia carrying heterozygous mutations in the RYR2 gene. . 2020-05-00. Pubmed ID: 32315959; DOI: 10.1016/j.scr.2020.101764 LUMCi020-ALUMCi021-A 2020-05-00 2020-05-00 PubMed: 32315959 DOI: 10.1016/j.scr.2020.101764Associated cell lines:
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Alexeeva V, Aydin IT, Schaniel C, Stranahan AW, D'Souza SL, Bieker JJ
A human H1-HBB11-GFP reporter embryonic stem cell line (WAe001-A-2) generated using TALEN-based genome editing
Alexeeva V et al. A human H1-HBB11-GFP reporter embryonic stem cell line (WAe001-A-2) generated using TALEN-based genome editing. . 2020-05-00. Pubmed ID: 32413789; DOI: 10.1016/j.scr.2020.101837; PMC: PMC7297435 WAe001-AWAe001-A-2 2020-05-00 2020-05-00 PubMed: 32413789 DOI: 10.1016/j.scr.2020.101837Associated cell lines:
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Chen S, Luo Z, Ward C, Ibañez DP, Liu H, Zhong X, Sharma NK, Qin B, Fan W, Wang D
Generation of two LRRK2 homozygous knockout human induced pluripotent stem cell lines using CRISPR/Cas9
Chen S et al. Generation of two LRRK2 homozygous knockout human induced pluripotent stem cell lines using CRISPR/Cas9. . 2020-05-00. Pubmed ID: 32339904; DOI: 10.1016/j.scr.2020.101804 GIBHi002-AGIBHi002-A-3GIBHi002-A-4 2020-05-00 2020-05-00 PubMed: 32339904 DOI: 10.1016/j.scr.2020.101804Associated cell lines:
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Zhang H, Ma Y, Lv Y, Wan Y, Zhao Q, Gai Z, Liu Y
An integration-free iPSC line SDQLCHi025-A from a girl with multiminicore disease carrying compound heterozygote mutations in RYR1 gene
Zhang H et al. An integration-free iPSC line SDQLCHi025-A from a girl with multiminicore disease carrying compound heterozygote mutations in RYR1 gene. . 2020-05-00. Pubmed ID: 32272370; DOI: 10.1016/j.scr.2020.101775 SDQLCHi025-A 2020-05-00 2020-05-00 PubMed: 32272370 DOI: 10.1016/j.scr.2020.101775Associated cell lines:
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Arai Y, Takami M, An Y, Matsuo-Takasaki M, Hemmi Y, Wakabayashi T, Inoue J, Noguchi M, Nakamura Y, Sugimoto K, Takemura T, Okita K, Osafune K, Takasato M, Hayata T, Hayashi Y
Generation of two human induced pluripotent stem cell lines derived from two juvenile nephronophthisis patients with NPHP1 deletion
Arai Y et al. Generation of two human induced pluripotent stem cell lines derived from two juvenile nephronophthisis patients with NPHP1 deletion. . 2020-05-00. Pubmed ID: 32361464; DOI: 10.1016/j.scr.2020.101815 BRCi010-ABRCi011-A 2020-05-00 2020-05-00 PubMed: 32361464 DOI: 10.1016/j.scr.2020.101815 -
Grosch M, Ittermann S, Rusha E, Greisle T, Ori C, Truong DJ, O'Neill AC, Pertek A, Westmeyer GG, Drukker M
Nucleus size and DNA accessibility are linked to the regulation of paraspeckle formation in cellular differentiation
Grosch M et al. Nucleus size and DNA accessibility are linked to the regulation of paraspeckle formation in cellular differentiation. . 2020-04-22. Pubmed ID: 32321486; DOI: 10.1186/s12915-020-00770-y; PMC: PMC7178590 MHHi006-AMHHi006-A-2 2020-04-22 2020-04-22 PubMed: 32321486 DOI: 10.1186/s12915-020-00770-yAssociated cell lines:
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Zumwalt M, Reddy AP
Stem Cells for Treatment of Musculoskeletal Conditions - Orthopaedic/Sports Medicine Applications
Zumwalt M et al. Stem Cells for Treatment of Musculoskeletal Conditions - Orthopaedic/Sports Medicine Applications. . 2020-04-01. Pubmed ID: 31794866; DOI: 10.1016/j.bbadis.2019.165624 CCMi003-ASDQLCHi004-A 2020-04-01 2020-04-01 PubMed: 31794866 DOI: 10.1016/j.bbadis.2019.165624Associated cell lines:
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Ali G, Elsayed AK, Nandakumar M, Bashir M, Younis I, Abu Aqel Y, Memon B, Temanni R, Abubaker F, Taheri S, Abdelalim EM
Keratinocytes Derived from Patient-Specific Induced Pluripotent Stem Cells Recapitulate the Genetic Signature of Psoriasis Disease
Ali G et al. Keratinocytes Derived from Patient-Specific Induced Pluripotent Stem Cells Recapitulate the Genetic Signature of Psoriasis Disease. . 2020-04-01. Pubmed ID: 31996098; DOI: 10.1089/scd.2019.0150; PMC: PMC7153648 QBRIi001-AQBRIi002-AQBRIi001-BQBRIi001-CQBRIi002-BQBRIi002-CQBRIi005-AQBRIi005-BQBRIi005-CQBRIi006-AQBRIi006-BQBRIi006-C 2020-04-01 2020-04-01 PubMed: 31996098 DOI: 10.1089/scd.2019.0150Associated cell lines:
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Page S, Patel R, Raut S, Al-Ahmad A
Neurological diseases at the blood-brain barrier: Stemming new scientific paradigms using patient-derived induced pluripotent cells
Page S et al. Neurological diseases at the blood-brain barrier: Stemming new scientific paradigms using patient-derived induced pluripotent cells. . 2020-04-01. Pubmed ID: 30593893; DOI: 10.1016/j.bbadis.2018.12.009 FUi002-A 2020-04-01 2020-04-01 PubMed: 30593893 DOI: 10.1016/j.bbadis.2018.12.009Associated cell lines:
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Hübscher D, Rebs S, Maurer W, Ghadri JR, Dressel R, Templin C, Streckfuss-Bömeke K
Generation of iPSC-lines from two independent Takotsubo syndrome patients with recurrent Takotsubo events
Hübscher D et al. Generation of iPSC-lines from two independent Takotsubo syndrome patients with recurrent Takotsubo events. . 2020-04-00. Pubmed ID: 32302918; DOI: 10.1016/j.scr.2020.101746 UMGi145-AUMGi146-A 2020-04-00 2020-04-00 PubMed: 32302918 DOI: 10.1016/j.scr.2020.101746 -
Li R, Pradhan M, Xu M, Roeder A, Beers J, Zou J, Liu C, Porter FD, Zheng W
An induced pluripotent stem cell line (TRNDi001-D) from a Niemann-Pick disease type C1 (NPC1) patient carrying a homozygous p. I1061T (c. 3182T>C) mutation in the NPC1 gene
Li R et al. An induced pluripotent stem cell line (TRNDi001-D) from a Niemann-Pick disease type C1 (NPC1) patient carrying a homozygous p. I1061T (c. 3182T>C) mutation in the NPC1 gene. . 2020-04-00. Pubmed ID: 32114296; DOI: 10.1016/j.scr.2020.101737; PMC: PMC7218921 TRNDi001-D 2020-04-00 2020-04-00 PubMed: 32114296 DOI: 10.1016/j.scr.2020.101737Associated cell lines:
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Datta I, Sowmithra, Jagtap S, Potdar C, Yadav R, Pal P
Generation of induced pluripotent stem cells (NIMHi001-A) from a Parkinson's disease patient of East Indian ethnicity carrying LRRK2 I1371V variant
Datta I et al. Generation of induced pluripotent stem cells (NIMHi001-A) from a Parkinson's disease patient of East Indian ethnicity carrying LRRK2 I1371V variant. . 2020-04-00. Pubmed ID: 32244201; DOI: 10.1016/j.scr.2020.101768 NIMHi001-A 2020-04-00 2020-04-00 PubMed: 32244201 DOI: 10.1016/j.scr.2020.101768Associated cell lines:
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Yang T, Qin J, Zhang Q, Sun H, Wang Z, Yang J, Liu H, Zhang C, Zhang S, Zhang J, Wang Y, Xu Y
Generation of induced pluripotent stem cell line (ZZUi0018-A ) from a patient with spinocerebellar ataxia type 6
Yang T et al. Generation of induced pluripotent stem cell line (ZZUi0018-A ) from a patient with spinocerebellar ataxia type 6. . 2020-04-00. Pubmed ID: 32229428; DOI: 10.1016/j.scr.2020.101777 ZZUi018-A 2020-04-00 2020-04-00 PubMed: 32229428 DOI: 10.1016/j.scr.2020.101777Associated cell lines:
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Zhang J, Wei L, Chen D, Feng L, Wu C, Wang R, Li X, Liu H
Generation of an integration-free induced pluripotent stem cell (iPSC) line (ZZUNEUi004-A) from a Wilson's disease patient harboring a homozygous Pro992Leu mutation in ATP7B gene
Zhang J et al. Generation of an integration-free induced pluripotent stem cell (iPSC) line (ZZUNEUi004-A) from a Wilson's disease patient harboring a homozygous Pro992Leu mutation in ATP7B gene. . 2020-04-00. Pubmed ID: 32113134; DOI: 10.1016/j.scr.2020.101741 ZZUNEUi004-A 2020-04-00 2020-04-00 PubMed: 32113134 DOI: 10.1016/j.scr.2020.101741Associated cell lines:
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Zhou Y, Ding C, Xia S, Jing Y, Mao S, Liu J, Chen J, Chan HF, Tang S, Chen J
Establishment of induced pluripotent stem cell line CSUASOi003- A from an autosomal recessive retinitis pigmentosa patient carrying compound heterozygous mutations in CRB1 gene
Zhou Y et al. Establishment of induced pluripotent stem cell line CSUASOi003- A from an autosomal recessive retinitis pigmentosa patient carrying compound heterozygous mutations in CRB1 gene. . 2020-04-00. Pubmed ID: 32244200; DOI: 10.1016/j.scr.2020.101742 CSUASOi003-A 2020-04-00 2020-04-00 PubMed: 32244200 DOI: 10.1016/j.scr.2020.101742Associated cell lines:
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Tembe S, Fernandes S, Khan N, Melinkeri S, Kale V, Limaye L
Establishment of human iPSC line from patient of Indian ethnicity carrying homozygous CD8/9 (+G) beta thalassemia mutation
Tembe S et al. Establishment of human iPSC line from patient of Indian ethnicity carrying homozygous CD8/9 (+G) beta thalassemia mutation. . 2020-04-00. Pubmed ID: 32278313; DOI: 10.1016/j.scr.2020.101772 NCCSi009-A 2020-04-00 2020-04-00 PubMed: 32278313 DOI: 10.1016/j.scr.2020.101772Associated cell lines:
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Xiao C, Yu M, Liu J, Wu H, Deng M, Zhang Q, Xiao X
Generation of an isogenic gene-corrected iPSC line (PUMCHi001-A-1) from a familial partial lipodystrophy type 2 (FPLD2) patient with a heterozygous R349W mutation in the LMNA gene
Xiao C et al. Generation of an isogenic gene-corrected iPSC line (PUMCHi001-A-1) from a familial partial lipodystrophy type 2 (FPLD2) patient with a heterozygous R349W mutation in the LMNA gene. . 2020-04-00. Pubmed ID: 32213461; DOI: 10.1016/j.scr.2020.101753 PUMCHi001-APUMCHi001-A-1 2020-04-00 2020-04-00 PubMed: 32213461 DOI: 10.1016/j.scr.2020.101753Associated cell lines:
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Huo Y, Wang J, He J, Kong D, Ma J
Establishment of human induced pluripotent stem cell line from dermal fibroblasts of a healthy individual
Huo Y et al. Establishment of human induced pluripotent stem cell line from dermal fibroblasts of a healthy individual. . 2020-04-00. Pubmed ID: 32224419; DOI: 10.1016/j.scr.2020.101762 DHMCi005-AHEBHMUi002-AHEBHMUi005-A 2020-04-00 2020-04-00 PubMed: 32224419 DOI: 10.1016/j.scr.2020.101762Associated cell lines:
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Ma J, Feng B, Kong D, He J, Guo R, Amponsah AE, Zhang W, Zhang S, Lv F, Song Y, Liu A, Cui H
Production and validation of human induced pluripotent stem cell line from sporadic amyotrophic lateral sclerosis (SALS)
Ma J et al. Production and validation of human induced pluripotent stem cell line from sporadic amyotrophic lateral sclerosis (SALS). . 2020-04-00. Pubmed ID: 32203916; DOI: 10.1016/j.scr.2020.101760 HEBHMUi002-AHEBHMUi003-A 2020-04-00 2020-04-00 PubMed: 32203916 DOI: 10.1016/j.scr.2020.101760Associated cell lines:
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Shuvalova LD, Eremeev AV, Bogomazova AN, Novosadova EV, Zerkalenkova EA, Olshanskaya YV, Fedotova EY, Glagoleva ES, Illarioshkin SN, Lebedeva OS, Lagarkova MA
Generation of induced pluripotent stem cell line RCPCMi004-A derived from patient with Parkinson's disease with deletion of the exon 2 in PARK2 gene
Shuvalova LD et al. Generation of induced pluripotent stem cell line RCPCMi004-A derived from patient with Parkinson's disease with deletion of the exon 2 in PARK2 gene. . 2020-04-00. Pubmed ID: 32151951; DOI: 10.1016/j.scr.2020.101733 RCPCMi004-A 2020-04-00 2020-04-00 PubMed: 32151951 DOI: 10.1016/j.scr.2020.101733Associated cell lines:
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de la Cruz BM, Ding Y, McInerney V, Krawczyk J, Lu Y, Yang G, Qian X, Li W, Howard L, Allen NM, O'Brien T, Gallagher L, Shen S
Derivation of two iPSC lines from a sporadic ASD patient (NUIGi033-A) and a paternal control (NUIGi034-A)
de la Cruz BM et al. Derivation of two iPSC lines from a sporadic ASD patient (NUIGi033-A) and a paternal control (NUIGi034-A). . 2020-04-00. Pubmed ID: 32097875; DOI: 10.1016/j.scr.2020.101722 NUIGi033-ANUIGi034-A 2020-04-00 2020-04-00 PubMed: 32097875 DOI: 10.1016/j.scr.2020.101722Associated cell lines:
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Pichard L, Brondelo JM, Becker F, Desprat R, De Ceuninck F, Pastoureau P, Noel D, Jorgensen C, Lemaitre JM
Generation of human pluripotent stem cell lines (iPSCs) from mesenchymal stem cells (MSCs) from three elderly patients with osteoarthritis
Pichard L et al. Generation of human pluripotent stem cell lines (iPSCs) from mesenchymal stem cells (MSCs) from three elderly patients with osteoarthritis. . 2020-04-00. Pubmed ID: 32200258; DOI: 10.1016/j.scr.2020.101721 REGUi003-AREGUi006-AREGUi007-AREGUi008-A 2020-04-00 2020-04-00 PubMed: 32200258 DOI: 10.1016/j.scr.2020.101721Associated cell lines:
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Elsayed AK, Aghadi M, Al-Khawaga S, Hussain K, Abdelalim EM
Derivation of a human induced pluripotent stem cell line (QBRIi007-A) from a patient carrying a homozygous intronic mutation (c.613-7T>G) in the SLC2A2 gene
Elsayed AK et al. Derivation of a human induced pluripotent stem cell line (QBRIi007-A) from a patient carrying a homozygous intronic mutation (c.613-7T>G) in the SLC2A2 gene. . 2020-04-00. Pubmed ID: 32146263; DOI: 10.1016/j.scr.2020.101736 QBRIi007-A 2020-04-00 2020-04-00 PubMed: 32146263 DOI: 10.1016/j.scr.2020.101736Associated cell lines:
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Merkert S, Schubert M, Haase A, Janssens HM, Scholte B, Lachmann N, Göhring G, Martin U
Generation of an induced pluripotent stem cell line (MHHi018-A) from a patient with Cystic Fibrosis carrying p.Asn1303Lys (N1303K) mutation
Merkert S et al. Generation of an induced pluripotent stem cell line (MHHi018-A) from a patient with Cystic Fibrosis carrying p.Asn1303Lys (N1303K) mutation. . 2020-04-00. Pubmed ID: 32220772; DOI: 10.1016/j.scr.2020.101744 MHHi018-A 2020-04-00 2020-04-00 PubMed: 32220772 DOI: 10.1016/j.scr.2020.101744Associated cell lines:
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Zhang B, Wang Y, Peng J, Hao Y, Guan Y
Generation of a human induced pluripotent stem cell line from an epilepsy patient carrying mutations in the PIK3R2 gene
Zhang B et al. Generation of a human induced pluripotent stem cell line from an epilepsy patient carrying mutations in the PIK3R2 gene. . 2020-04-00. Pubmed ID: 32155459; DOI: 10.1016/j.scr.2020.101711 SJTUi001-A 2020-04-00 2020-04-00 PubMed: 32155459 DOI: 10.1016/j.scr.2020.101711Associated cell lines:
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Rehakova D, Souralova T, Koutna I
Clinical-Grade Human Pluripotent Stem Cells for Cell Therapy: Characterization Strategy
Rehakova D et al. Clinical-Grade Human Pluripotent Stem Cells for Cell Therapy: Characterization Strategy. . 2020-03-31. Pubmed ID: 32244538; DOI: 10.3390/ijms21072435; PMC: PMC7177280 RCe013-ARCe015-A 2020-03-31 2020-03-31 PubMed: 32244538 DOI: 10.3390/ijms21072435 -
Secardin L, Limia CEG, di Stefano A, Bonamino MH, Saliba J, Kataoka K, Rehen SK, Raslova H, Marty C, Ogawa S, Vainchenker W, Monte-Mor BDCR, Plo I
TET2 haploinsufficiency alters reprogramming into induced pluripotent stem cells
Secardin L et al. TET2 haploinsufficiency alters reprogramming into induced pluripotent stem cells. . 2020-04-00. Pubmed ID: 32193150; DOI: 10.1016/j.scr.2020.101755 INCABRi002-A 2020-04-00 2020-04-00 PubMed: 32193150 DOI: 10.1016/j.scr.2020.101755Associated cell lines:
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Bchetnia M, Martineau L, Racine V, Powell J, McCuaig C, Puymirat J, Laprise C
Generation of a human induced pluripotent stem cell line (UQACi001-A) from a severe epidermolysis bullosa simplex patient with the heterozygous mutation p.R125S in the KRT14 gene
Bchetnia M et al. Generation of a human induced pluripotent stem cell line (UQACi001-A) from a severe epidermolysis bullosa simplex patient with the heterozygous mutation p.R125S in the KRT14 gene. . 2020-04-00. Pubmed ID: 32179493; DOI: 10.1016/j.scr.2020.101748 UQACi001-A 2020-04-00 2020-04-00 PubMed: 32179493 DOI: 10.1016/j.scr.2020.101748Associated cell lines:
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Zhou W, Ma D, Tan EK
Mitochondrial CHCHD2 and CHCHD10: Roles in Neurological Diseases and Therapeutic Implications
Zhou W et al. Mitochondrial CHCHD2 and CHCHD10: Roles in Neurological Diseases and Therapeutic Implications. . 2020-04-00. Pubmed ID: 31526091; DOI: 10.1177/1073858419871214 ZZUi007-A 2020-04-00 2020-04-00 PubMed: 31526091 DOI: 10.1177/1073858419871214Associated cell lines:
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Fatima A, Schuster J, Akram T, Sobol M, Hoeber J, Dahl N
Generation of a human Neurochondrin deficient iPSC line KICRi002-A-3 using CRISPR/Cas9
Fatima A et al. Generation of a human Neurochondrin deficient iPSC line KICRi002-A-3 using CRISPR/Cas9. . 2020-04-00. Pubmed ID: 32203915; DOI: 10.1016/j.scr.2020.101758 KICRi002-AKICRi002-A-3 2020-04-00 2020-04-00 PubMed: 32203915 DOI: 10.1016/j.scr.2020.101758Associated cell lines:
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Lin HY, Tsai LK, Cheng YC, Lu HE, Huang CY, Hsieh PCH, Lin CH
Generation of a human induced pluripotent stem cell (iPSC) line (IBMS-iPSC-048-05) from a patient with ALS and parkinsonism having a hexanucleotide repeat expansion mutation in C9orf72 gene
Lin HY et al. Generation of a human induced pluripotent stem cell (iPSC) line (IBMS-iPSC-048-05) from a patient with ALS and parkinsonism having a hexanucleotide repeat expansion mutation in C9orf72 gene. . 2020-04-00. Pubmed ID: 32151952; DOI: 10.1016/j.scr.2020.101734 IBMSi019-A 2020-04-00 2020-04-00 PubMed: 32151952 DOI: 10.1016/j.scr.2020.101734Associated cell lines:
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Yang M, Liu M, Ding Y, Vajda A, Ma J, Cui H, O'Brien T, Henshall D, Hardiman O, Shen S
Generation of twelve induced pluripotent stem cell lines from two healthy controls and two patients with sporadic amyotrophic lateral sclerosis
Yang M et al. Generation of twelve induced pluripotent stem cell lines from two healthy controls and two patients with sporadic amyotrophic lateral sclerosis. . 2020-04-00. Pubmed ID: 32208303; DOI: 10.1016/j.scr.2020.101752 NUIGi048-ANUIGi048-BNUIGi048-CNUIGi049-ANUIGi049-BNUIGi049-CNUIGi050-ANUIGi050-BNUIGi050-CNUIGi051-ANUIGi051-BNUIGi051-C 2020-04-00 2020-04-00 PubMed: 32208303 DOI: 10.1016/j.scr.2020.101752Associated cell lines:
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Slot E, de Klein A, Rottier RJ
Generation of three iPSC lines from two patients with heterozygous FOXF1 mutations associated to Alveolar Capillary Dysplasia with Misalignment of the Pulmonary Veins
Slot E et al. Generation of three iPSC lines from two patients with heterozygous FOXF1 mutations associated to Alveolar Capillary Dysplasia with Misalignment of the Pulmonary Veins. . 2020-04-00. Pubmed ID: 32169823; DOI: 10.1016/j.scr.2020.101745 EMCi127-AEMCi127-BEMCi128-A 2020-04-00 2020-04-00 PubMed: 32169823 DOI: 10.1016/j.scr.2020.101745 -
Vasconcelos E Sá J, Simão D, Terrasso AP, Silva MM, Brito C, Isidro IA, Alves PM, Carrondo MJT
Unveiling dynamic metabolic signatures in human induced pluripotent and neural stem cells
Vasconcelos E Sá J et al. Unveiling dynamic metabolic signatures in human induced pluripotent and neural stem cells. . 2020-04-00. Pubmed ID: 32298259; DOI: 10.1371/journal.pcbi.1007780; PMC: PMC7188302 RIi001-A 2020-04-00 2020-04-00 PubMed: 32298259 DOI: 10.1371/journal.pcbi.1007780Associated cell lines:
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Fatima A, Schuster J, Akram T, González CM, Sobol M, Hoeber J, Dahl N
Incontinentia pigmenti: Generation of an IKBKG deficient human iPSC line (KICRi002-A-1) on a 46,XY background using CRISPR/Cas9
Fatima A et al. Incontinentia pigmenti: Generation of an IKBKG deficient human iPSC line (KICRi002-A-1) on a 46,XY background using CRISPR/Cas9. . 2020-04-00. Pubmed ID: 32126327; DOI: 10.1016/j.scr.2020.101739 KICRi002-AKICRi002-A-1 2020-04-00 2020-04-00 PubMed: 32126327 DOI: 10.1016/j.scr.2020.101739Associated cell lines:
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Wang P, Wang J, Xing Y, Wang H, Yu D, Feng Y, Wu H, Wu Y, Chen Z, Wang J, Shi H
Establishment of an iPSC line (JTUi002-A) from a patient with Waardenburg syndrome caused by a SOX10 mutation and carrying a GJB2 mutation
Wang P et al. Establishment of an iPSC line (JTUi002-A) from a patient with Waardenburg syndrome caused by a SOX10 mutation and carrying a GJB2 mutation. . 2020-04-00. Pubmed ID: 32199281; DOI: 10.1016/j.scr.2020.101756 JTUi002-A 2020-04-00 2020-04-00 PubMed: 32199281 DOI: 10.1016/j.scr.2020.101756Associated cell lines:
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Malakhova AA, Grigor'eva EV, Malankhanova TB, Pavlova SV, Valetdinova KR, Abramycheva NY, Vetchinova AS, Illarioshkin SN, Zakian SM
Generation of induced pluripotent stem cell line ICGi018-A from peripheral blood mononuclear cells of a patient with Huntington's disease
Malakhova AA et al. Generation of induced pluripotent stem cell line ICGi018-A from peripheral blood mononuclear cells of a patient with Huntington's disease. . 2020-04-00. Pubmed ID: 32179492; DOI: 10.1016/j.scr.2020.101743 ICGi018-A 2020-04-00 2020-04-00 PubMed: 32179492 DOI: 10.1016/j.scr.2020.101743Associated cell lines:
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Fang YH, Wang SPH, Gao ZH, Wu SN, Chang HY, Yang PJ, Liu PY, Liu YW
Efficient Cardiac Differentiation of Human Amniotic Fluid-Derived Stem Cells into Induced Pluripotent Stem Cells and Their Potential Immune Privilege
Fang YH et al. Efficient Cardiac Differentiation of Human Amniotic Fluid-Derived Stem Cells into Induced Pluripotent Stem Cells and Their Potential Immune Privilege. . 2020-03-29. Pubmed ID: 32235313; DOI: 10.3390/ijms21072359; PMC: PMC7177657 NCKUi001-A 2020-03-29 2020-03-29 PubMed: 32235313 DOI: 10.3390/ijms21072359Associated cell lines:
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van Riet S, Ninaber DK, Mikkers HMM, Tetley TD, Jost CR, Mulder AA, Pasman T, Baptista D, Poot AA, Truckenmüller R, Mummery CL, Freund C, Rottier RJ, Hiemstra PS
In vitro modelling of alveolar repair at the air-liquid interface using alveolar epithelial cells derived from human induced pluripotent stem cells
van Riet S et al. In vitro modelling of alveolar repair at the air-liquid interface using alveolar epithelial cells derived from human induced pluripotent stem cells. . 2020-03-26. Pubmed ID: 32218519; DOI: 10.1038/s41598-020-62226-1; PMC: PMC7099095 LUMCi031-A 2020-03-26 2020-03-26 PubMed: 32218519 DOI: 10.1038/s41598-020-62226-1Associated cell lines:
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Thompson O, von Meyenn F, Hewitt Z, Alexander J, Wood A, Weightman R, Gregory S, Krueger F, Andrews S, Barbaric I, Gokhale PJ, Moore HD, Reik W, Milo M, Nik-Zainal S, Yusa K, Andrews PW
Low rates of mutation in clinical grade human pluripotent stem cells under different culture conditions
Thompson O et al. Low rates of mutation in clinical grade human pluripotent stem cells under different culture conditions. . 2020-03-23. Pubmed ID: 32251294; DOI: 10.1038/s41467-020-15271-3; PMC: PMC7089967 UOSe009-A 2020-03-23 2020-03-23 PubMed: 32251294 DOI: 10.1038/s41467-020-15271-3Associated cell lines:
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Frew J, Baradaran-Heravi A, Balgi AD, Wu X, Yan TD, Arns S, Shidmoossavee FS, Tan J, Jaquith JB, Jansen-West KR, Lynn FC, Gao FB, Petrucelli L, Feldman HH, Mackenzie IR, Roberge M, Nygaard HB
Premature termination codon readthrough upregulates progranulin expression and improves lysosomal function in preclinical models of GRN deficiency
Frew J et al. Premature termination codon readthrough upregulates progranulin expression and improves lysosomal function in preclinical models of GRN deficiency. . 2020-03-16. Pubmed ID: 32178712; DOI: 10.1186/s13024-020-00369-5; PMC: PMC7075020 UBCi001-A 2020-03-16 2020-03-16 PubMed: 32178712 DOI: 10.1186/s13024-020-00369-5Associated cell lines:
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Okubo T, Hayashi R, Shibata S, Kudo Y, Ishikawa Y, Inoue S, Kobayashi Y, Honda A, Honma Y, Kawasaki S, Nishida K
Generation and validation of a PITX2-EGFP reporter line of human induced pluripotent stem cells enables isolation of periocular mesenchymal cells
Okubo T et al. Generation and validation of a PITX2-EGFP reporter line of human induced pluripotent stem cells enables isolation of periocular mesenchymal cells. . 2020-03-13. Pubmed ID: 32034090; DOI: 10.1074/jbc.ra119.010713; PMC: PMC7076207 KUIFMSi004-C 2020-03-13 2020-03-13 PubMed: 32034090 DOI: 10.1074/jbc.ra119.010713Associated cell lines:
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Boon R, Kumar M, Tricot T, Elia I, Ordovas L, Jacobs F, One J, De Smedt J, Eelen G, Bird M, Roelandt P, Doglioni G, Vriens K, Rossi M, Vazquez MA, Vanwelden T, Chesnais F, El Taghdouini A, Najimi M, Sokal E, Cassiman D, Snoeys J, Monshouwer M, Hu WS, Lange C, Carmeliet P, Fendt SM, Verfaillie CM
Amino acid levels determine metabolism and CYP450 function of hepatocytes and hepatoma cell lines
Boon R et al. Amino acid levels determine metabolism and CYP450 function of hepatocytes and hepatoma cell lines. . 2020-03-13. Pubmed ID: 32170132; DOI: 10.1038/s41467-020-15058-6; PMC: PMC7069944 SIGi001-A-23 2020-03-13 2020-03-13 PubMed: 32170132 DOI: 10.1038/s41467-020-15058-6Associated cell lines:
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Xu H, Jia Z, Ma K, Zhang J, Dai C, Yao Z, Deng W, Su J, Wang R, Chen X
Protective effect of BMSCs-derived exosomes mediated by BDNF on TBI via miR-216a-5p
Xu H et al. Protective effect of BMSCs-derived exosomes mediated by BDNF on TBI via miR-216a-5p. . 2020-03-09. Pubmed ID: 32150531; DOI: 10.12659/msm.920855; PMC: PMC7081927 NYGCe001-A 2020-03-09 2020-03-09 PubMed: 32150531 DOI: 10.12659/msm.920855Associated cell lines:
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Casamassa A, Ferrari D, Gelati M, Carella M, Vescovi AL, Rosati J
A Link between Genetic Disorders and Cellular Impairment, Using Human Induced Pluripotent Stem Cells to Reveal the Functional Consequences of Copy Number Variations in the Central Nervous System-A Close Look at Chromosome 15
Casamassa A et al. A Link between Genetic Disorders and Cellular Impairment, Using Human Induced Pluripotent Stem Cells to Reveal the Functional Consequences of Copy Number Variations in the Central Nervous System-A Close Look at Chromosome 15. . 2020-03-09. Pubmed ID: 32182809; DOI: 10.3390/ijms21051860; PMC: PMC7084702 EURACi001-AEURACi002-AEURACi003-ACSSi005-AIITi001-AVRFi001-ACCMi003-AEURACi005-AUNIBSi008-AUNIBSi008-BUNIBSi008-CSDQLCHi008-ASDQLCHi014-AICGi017-AQBRIi009-A 2020-03-09 2020-03-09 PubMed: 32182809 DOI: 10.3390/ijms21051860 -
Khadjeh S, Hindmarsh V, Weber F, Cyganek L, Vidal RO, Torkieh S, Streckfuss-Bömeke K, Lbik D, Tiburcy M, Mohamed BA, Bonn S, Toischer K, Hasenfuss G
CRISPLD1: a novel conserved target in the transition to human heart failure
Khadjeh S et al. CRISPLD1: a novel conserved target in the transition to human heart failure. . 2020-03-07. Pubmed ID: 32146539; DOI: 10.1007/s00395-020-0784-4; PMC: PMC7060963 UMGi014-BUMGi014-B-3 2020-03-07 2020-03-07 PubMed: 32146539 DOI: 10.1007/s00395-020-0784-4Associated cell lines:
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Castro-Viñuelas R, Sanjurjo-Rodríguez C, Piñeiro-Ramil M, Hermida-Gómez T, Rodríguez-Fernández S, Oreiro N, de Toro J, Fuentes I, Blanco FJ, Díaz-Prado S
Generation and characterization of human induced pluripotent stem cells (iPSCs) from hand osteoarthritis patient-derived fibroblasts
Castro-Viñuelas R et al. Generation and characterization of human induced pluripotent stem cells (iPSCs) from hand osteoarthritis patient-derived fibroblasts. . 2020-03-06. Pubmed ID: 32144293; DOI: 10.1038/s41598-020-61071-6; PMC: PMC7060311 ESi080-AESi083-AESi084-A 2020-03-06 2020-03-06 PubMed: 32144293 DOI: 10.1038/s41598-020-61071-6 -
Fang F, Li Z, Zhao Q, Xiong C, Ni K
Analysis of multi-lineage gene expression dynamics during primordial germ cell induction from human induced pluripotent stem cells
Fang F et al. Analysis of multi-lineage gene expression dynamics during primordial germ cell induction from human induced pluripotent stem cells. . 2020-03-04. Pubmed ID: 32127035; DOI: 10.1186/s13287-020-01620-y; PMC: PMC7055065 HUSTi001-A 2020-03-04 2020-03-04 PubMed: 32127035 DOI: 10.1186/s13287-020-01620-yAssociated cell lines:
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Pongpamorn P, Dahlmann J, Haase A, Ebeling CT, Merkert S, Göhring G, Lachmann N, Martens A, Haverich A, Martin U, Olmer R
Generation of three induced pluripotent stem cell lines (MHHi012-A, MHHi013-A, MHHi014-A) from a family with Loeys-Dietz syndrome carrying a heterozygous p.M253I (c.759G>A) mutation in the TGFBR1 gene
Pongpamorn P et al. Generation of three induced pluripotent stem cell lines (MHHi012-A, MHHi013-A, MHHi014-A) from a family with Loeys-Dietz syndrome carrying a heterozygous p.M253I (c.759G>A) mutation in the TGFBR1 gene. . 2020-03-00. Pubmed ID: 32062130; DOI: 10.1016/j.scr.2020.101707 MHHi012-AMHHi013-AMHHi014-A 2020-03-00 2020-03-00 PubMed: 32062130 DOI: 10.1016/j.scr.2020.101707 -
Ullah I, Busch JF, Rabien A, Ergün B, Stamm C, Knosalla C, Hippenstiel S, Reinke P, Kurtz A
Adult Tissue Extracellular Matrix Determines Tissue Specification of Human iPSC-Derived Embryonic Stage Mesodermal Precursor Cells
Ullah I et al. Adult Tissue Extracellular Matrix Determines Tissue Specification of Human iPSC-Derived Embryonic Stage Mesodermal Precursor Cells. . 2020-03-00. Pubmed ID: 32154066; DOI: 10.1002/advs.201901198; PMC: PMC7055561 WISCi004-ABCRTi005-ABIHi004-A 2020-03-00 2020-03-00 PubMed: 32154066 DOI: 10.1002/advs.201901198Associated cell lines:
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van den Brink L, Brandão KO, Yiangou L, Mol MPH, Grandela C, Mummery CL, Verkerk AO, Davis RP
Cryopreservation of human pluripotent stem cell-derived cardiomyocytes is not detrimental to their molecular and functional properties
van den Brink L et al. Cryopreservation of human pluripotent stem cell-derived cardiomyocytes is not detrimental to their molecular and functional properties. . 2020-03-00. Pubmed ID: 31945612; DOI: 10.1016/j.scr.2019.101698; PMC: PMC7611364 LUMCi004-ALUMCi028-A 2020-03-00 2020-03-00 PubMed: 31945612 DOI: 10.1016/j.scr.2019.101698Associated cell lines:
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Xu C, Zhou Z, Liu C, Kang X, Zhong X, Zhang Q, Xu Y
Generation of a DAPK1 knockout first (conditional ready) human embryonic stem cell line (ZSSYe001-A) by CRISPR-Cas9 technology
Xu C et al. Generation of a DAPK1 knockout first (conditional ready) human embryonic stem cell line (ZSSYe001-A) by CRISPR-Cas9 technology. . 2020-03-00. Pubmed ID: 31978714; DOI: 10.1016/j.scr.2019.101693 ZSSYe001-A 2020-03-00 2020-03-00 PubMed: 31978714 DOI: 10.1016/j.scr.2019.101693Associated cell lines:
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Gripp KW, Schill L, Schoyer L, Stronach B, Bennett AM, Blaser S, Brown A, Burdine R, Burkitt-Wright E, Castel P, Darilek S, Dias A, Dyer T, Ellis M, Erickson G, Gelb BD, Green T, Gross A, Ho A, Holder JL Jr, Inoue SI, Jelin AC, Kennedy A, Klein R, Kontaridis MI, Magoulas P, McConnell DB, McCormick F, Neel BG, Prada CE, Rauen KA, Roberts A, Rodriguez-Viciana P, Rosen N, Rumbaugh G, Sablina A, Solman M, Tartaglia M, Thomas A, Timmer WC, Venkatachalam K, Walsh KS, Wolters PL, Yi JS, Zenker M, Ratner N
The sixth international RASopathies symposium: Precision medicine-From promise to practice
Gripp KW et al. The sixth international RASopathies symposium: Precision medicine-From promise to practice. . 2020-03-00. Pubmed ID: 31825160; DOI: 10.1002/ajmg.a.61434; PMC: PMC7021559 TRNDi003-A 2020-03-00 2020-03-00 PubMed: 31825160 DOI: 10.1002/ajmg.a.61434Associated cell lines:
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Puentes-Tellez MA, Lerma-Barbosa PA, Garzón-Jaramillo RG, Suarez DA, Espejo-Mojica AJ, Guevara JM, Echeverri OY, Solano-Galarza D, Uribe-Ardila A, Alméciga-Díaz CJ
A perspective on research, diagnosis, and management of lysosomal storage disorders in Colombia
Puentes-Tellez MA et al. A perspective on research, diagnosis, and management of lysosomal storage disorders in Colombia. . 2020-03-00. Pubmed ID: 32258481; DOI: 10.1016/j.heliyon.2020.e03635; PMC: PMC7113438 TRNDi005-A 2020-03-00 2020-03-00 PubMed: 32258481 DOI: 10.1016/j.heliyon.2020.e03635Associated cell lines:
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Ferrari G, Muntoni F, Tedesco FS
Generation of two genomic-integration-free DMD iPSC lines with mutations affecting all dystrophin isoforms and potentially amenable to exon-skipping
Ferrari G et al. Generation of two genomic-integration-free DMD iPSC lines with mutations affecting all dystrophin isoforms and potentially amenable to exon-skipping. . 2020-03-00. Pubmed ID: 32087527; DOI: 10.1016/j.scr.2019.101688; PMC: PMC7057262 UCLi011-AUCLi012-A 2020-03-00 2020-03-00 PubMed: 32087527 DOI: 10.1016/j.scr.2019.101688 -
Cordes M, Bucichowski P, Alfaar AS, Tsang SH, Almedawar S, Reichhart N, Strauß O
Inhibition of Ca(2+) channel surface expression by mutant bestrophin-1 in RPE cells
Cordes M et al. Inhibition of Ca(2+) channel surface expression by mutant bestrophin-1 in RPE cells. . 2020-03-00. Pubmed ID: 31930599; DOI: 10.1096/fj.201901202rr CRTDi004-A 2020-03-00 2020-03-00 PubMed: 31930599 DOI: 10.1096/fj.201901202rrAssociated cell lines:
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Khudiakov A, Perepelina K, Klauzen P, Zlotina A, Gusev K, Kaznacheyeva E, Malashicheva A, Kostareva A
Generation of two iPSC lines (FAMRCi004-A and FAMRCi004-B) from patient with familial progressive cardiac conduction disorder carrying genetic variant DSP p.His1684Arg
Khudiakov A et al. Generation of two iPSC lines (FAMRCi004-A and FAMRCi004-B) from patient with familial progressive cardiac conduction disorder carrying genetic variant DSP p.His1684Arg. . 2020-03-00. Pubmed ID: 32062131; DOI: 10.1016/j.scr.2020.101720 FAMRCi004-AFAMRCi004-B 2020-03-00 2020-03-00 PubMed: 32062131 DOI: 10.1016/j.scr.2020.101720Associated cell lines:
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Jin P, Wang S, Jiang X, Shan X, Jiang S, Quan Y, Zhang T, Yang J, Zhang H, Ma J, Dong M, Fan J, Fan X, Gong Y, Wang Y
Generation of human induced pluripotent stem cell line (WMUi001-A) from a patient with aortic dissection
Jin P et al. Generation of human induced pluripotent stem cell line (WMUi001-A) from a patient with aortic dissection. . 2020-03-00. Pubmed ID: 32062133; DOI: 10.1016/j.scr.2020.101730 WMUi001-A 2020-03-00 2020-03-00 PubMed: 32062133 DOI: 10.1016/j.scr.2020.101730Associated cell lines:
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Ding Y, Carvalho E, Murphy C, McInerney V, Krawczyk J, O'Brien T, Howard L, Cai L, Shen S
Derivation of familial iPSC lines from three patients with retinitis pigmentosa carrying an autosomal dominant RPE65 mutation (NUIGi027-A, NUIGi028-A, NUIGi029-A)
Ding Y et al. Derivation of familial iPSC lines from three patients with retinitis pigmentosa carrying an autosomal dominant RPE65 mutation (NUIGi027-A, NUIGi028-A, NUIGi029-A). . 2020-03-00. Pubmed ID: 31954326; DOI: 10.1016/j.scr.2019.101665 NUIGi027-ANUIGi028-ANUIGi029-A 2020-03-00 2020-03-00 PubMed: 31954326 DOI: 10.1016/j.scr.2019.101665Associated cell lines:
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Fuchs NV, Schieck M, Neuenkirch M, Tondera C, Schmitz H, Wendeburg L, Steinemann D, Elpers C, Rutsch F, König R
Generation of three induced pluripotent cell lines (iPSCs) from an Aicardi-Goutières syndrome (AGS) patient harboring a deletion in the genomic locus of the sterile alpha motif and HD domain containing protein 1 (SAMHD1)
Fuchs NV et al. Generation of three induced pluripotent cell lines (iPSCs) from an Aicardi-Goutières syndrome (AGS) patient harboring a deletion in the genomic locus of the sterile alpha motif and HD domain containing protein 1 (SAMHD1). . 2020-03-00. Pubmed ID: 32062129; DOI: 10.1016/j.scr.2019.101697 PEIi002-APEIi002-BPEIi002-C 2020-03-00 2020-03-00 PubMed: 32062129 DOI: 10.1016/j.scr.2019.101697 -
Liu X, Yang X, Li Y, Wang X, Ma J, Jiang W, Liu Y, Sun W, Gong Y
Generation of patient-specific pluripotent induced stem cell line SDUBMSI002-A from a patient with X-linked mental retardation syndrome
Liu X et al. Generation of patient-specific pluripotent induced stem cell line SDUBMSI002-A from a patient with X-linked mental retardation syndrome. . 2020-03-00. Pubmed ID: 32078988; DOI: 10.1016/j.scr.2020.101724 SDUBMSi002-A 2020-03-00 2020-03-00 PubMed: 32078988 DOI: 10.1016/j.scr.2020.101724Associated cell lines:
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Mao S, Ding C, Zhou Y, Jing Y, Chen J, Guo Y, Liu J, Cui Z, Yan X, Gu J, Wang Y, Chen J, Tang S
Establishment of a human induced pluripotent stem cell line (CSUASOi005-A), from peripheral blood mononuclear cells of a patient with X-linked juvenile retinoschisis carrying a novel mutation in RS1 gene
Mao S et al. Establishment of a human induced pluripotent stem cell line (CSUASOi005-A), from peripheral blood mononuclear cells of a patient with X-linked juvenile retinoschisis carrying a novel mutation in RS1 gene. . 2020-03-00. Pubmed ID: 32050117; DOI: 10.1016/j.scr.2020.101718 CSUASOi005-A 2020-03-00 2020-03-00 PubMed: 32050117 DOI: 10.1016/j.scr.2020.101718Associated cell lines:
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Yan YI, Qiu Y, Zhao A, Zhao J, Wang Y, Deng Y
Establishment of SIAISi001-A, an induced pluripotent stem cell (iPSC) line from 66-year old mild cognitive impairment (MCI) with two copies of APOE4 gene
Yan YI et al. Establishment of SIAISi001-A, an induced pluripotent stem cell (iPSC) line from 66-year old mild cognitive impairment (MCI) with two copies of APOE4 gene. . 2020-03-00. Pubmed ID: 32007762; DOI: 10.1016/j.scr.2020.101702 SIAISi001-A 2020-03-00 2020-03-00 PubMed: 32007762 DOI: 10.1016/j.scr.2020.101702Associated cell lines:
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Li M, Shin J, Risgaard RD, Parries MJ, Wang J, Chasman D, Liu S, Roy S, Bhattacharyya A, Zhao X
Identification of FMR1-regulated molecular networks in human neurodevelopment
Li M et al. Identification of FMR1-regulated molecular networks in human neurodevelopment. . 2020-03-00. Pubmed ID: 32179589; DOI: 10.1101/gr.251405.119; PMC: PMC7111522 WAe001-A-50WAe001-A-51WAe013-A-1WAe013-A-2 2020-03-00 2020-03-00 PubMed: 32179589 DOI: 10.1101/gr.251405.119Associated cell lines:
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Guan J, Li Z, Zhang H, Yang X, Ma Y, Li Y, Dong R, Gai Z, Liu Y
Generation of a Human iPSC line (SDQLCHi021-A) from a patient with methylmalonic acidemia cblC type carrying compound heterozygous mutations in MMAHC gene
Guan J et al. Generation of a Human iPSC line (SDQLCHi021-A) from a patient with methylmalonic acidemia cblC type carrying compound heterozygous mutations in MMAHC gene. . 2020-03-00. Pubmed ID: 32058304; DOI: 10.1016/j.scr.2020.101709 SDQLCHi021-A 2020-03-00 2020-03-00 PubMed: 32058304 DOI: 10.1016/j.scr.2020.101709Associated cell lines:
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Gatinois V, Desprat R, Becker F, Pichard L, Bernex F, Isidor B, Pellestor F, Lemaitre JM
iPSC line derived from a Bloom syndrome patient retains an increased disease-specific sister-chromatid exchange activity
Gatinois V et al. iPSC line derived from a Bloom syndrome patient retains an increased disease-specific sister-chromatid exchange activity. . 2020-03-00. Pubmed ID: 31918214; DOI: 10.1016/j.scr.2019.101696 REGUi003-AREGUi004-A 2020-03-00 2020-03-00 PubMed: 31918214 DOI: 10.1016/j.scr.2019.101696Associated cell lines:
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Wang J, Cui Y, Xing K, Luan J, Han J
Generation and characterization of a human iPSC line derived from congenital clubfoot amniotic fluid cells
Wang J et al. Generation and characterization of a human iPSC line derived from congenital clubfoot amniotic fluid cells. . 2020-03-00. Pubmed ID: 31986484; DOI: 10.1016/j.scr.2020.101712 SMBCi002-A 2020-03-00 2020-03-00 PubMed: 31986484 DOI: 10.1016/j.scr.2020.101712Associated cell lines:
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Panda A, Gurusamy N, Rajasingh S, Carter HK, Thomas EL, Rajasingh J
Non-viral reprogramming and induced pluripotent stem cells for cardiovascular therapy
Panda A et al. Non-viral reprogramming and induced pluripotent stem cells for cardiovascular therapy. . 2020-03-00. Pubmed ID: 31954271; DOI: 10.1016/j.diff.2019.12.001; PMC: PMC7138699 TRNDi003-A 2020-03-00 2020-03-00 PubMed: 31954271 DOI: 10.1016/j.diff.2019.12.001Associated cell lines:
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Lorthongpanich C, Laowtammathron C, Jiamvoraphong N, Srisook P, Chingsuwanrote P, Klaihmon P, Damkham N, Terbto P, Waeteekul S, U-Pratya Y, Issaragrisil S
YAP-depleted iPSC MUSIi012-A-2 maintained all normal stem cell characteristics
Lorthongpanich C et al. YAP-depleted iPSC MUSIi012-A-2 maintained all normal stem cell characteristics. . 2020-03-00. Pubmed ID: 32018207; DOI: 10.1016/j.scr.2020.101723 MUSIi012-AMUSIi012-A-2 2020-03-00 2020-03-00 PubMed: 32018207 DOI: 10.1016/j.scr.2020.101723Associated cell lines:
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Xiaojing W, Yanyan M, Ruonan D, Xiaolin L, Haiyan Z, Jian M, Yi L, Wenjie S, Qiji L
Generation of a human induced pluripotent stem cell line (SDUBMSi001-A) from a hereditary spastic paraplegia patient carrying kif1a c.773C>T missense mutation
Xiaojing W et al. Generation of a human induced pluripotent stem cell line (SDUBMSi001-A) from a hereditary spastic paraplegia patient carrying kif1a c.773C>T missense mutation. . 2020-03-00. Pubmed ID: 32045731; DOI: 10.1016/j.scr.2020.101727 SDUBMSi001-A 2020-03-00 2020-03-00 PubMed: 32045731 DOI: 10.1016/j.scr.2020.101727Associated cell lines:
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Fukunaga I, Shiga T, Chen C, Oe Y, Danzaki K, Ohta S, Matsuoka R, Anzai T, Hibiya-Motegi R, Tajima S, Ikeda K, Akamatsu W, Kamiya K
Generation of the induced pluripotent stem cell (hiPSC) line (JUFMDOi004-A) from a patient with hearing loss carrying GJB2 (p.V37I) mutation
Fukunaga I et al. Generation of the induced pluripotent stem cell (hiPSC) line (JUFMDOi004-A) from a patient with hearing loss carrying GJB2 (p.V37I) mutation. . 2020-03-00. Pubmed ID: 31926383; DOI: 10.1016/j.scr.2019.101674 JUFMDOi004-A 2020-03-00 2020-03-00 PubMed: 31926383 DOI: 10.1016/j.scr.2019.101674Associated cell lines:
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Azevedo C, Chumarina M, Serafimova E, Goldwurm S, Collin A, Roybon L, Savchenko E, Pomeshchik Y
Generation of an induced pluripotent stem cell line (CSC-32) from a patient with Parkinson's disease carrying a heterozygous variation p.A53T in the SNCA gene
Azevedo C et al. Generation of an induced pluripotent stem cell line (CSC-32) from a patient with Parkinson's disease carrying a heterozygous variation p.A53T in the SNCA gene. . 2020-03-00. Pubmed ID: 31954327; DOI: 10.1016/j.scr.2019.101694 ULUNDi008-A 2020-03-00 2020-03-00 PubMed: 31954327 DOI: 10.1016/j.scr.2019.101694Associated cell lines:
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Zhou HM, Zhou XQ, Lu JZ, Jia WW, Kang JH
An induced pluripotent stem cell line (SHEHi002-A (5426))from a patient of long QT syndrome type 8 with c.2573G>A mutation in the gene CACNA1C
Zhou HM et al. An induced pluripotent stem cell line (SHEHi002-A (5426))from a patient of long QT syndrome type 8 with c.2573G>A mutation in the gene CACNA1C. . 2020-03-00. Pubmed ID: 32062134; DOI: 10.1016/j.scr.2020.101731 SHEHi002-A 2020-03-00 2020-03-00 PubMed: 32062134 DOI: 10.1016/j.scr.2020.101731Associated cell lines:
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Sun C, Yang M, Qin F, Guo R, Liang S, Hu H
Generation of an induced pluripotent stem cell line SYSUi-003-A from a child with epilepsy carrying GRIN2A mutation
Sun C et al. Generation of an induced pluripotent stem cell line SYSUi-003-A from a child with epilepsy carrying GRIN2A mutation. . 2020-03-00. Pubmed ID: 32036246; DOI: 10.1016/j.scr.2020.101706 SYSUi003-A 2020-03-00 2020-03-00 PubMed: 32036246 DOI: 10.1016/j.scr.2020.101706Associated cell lines:
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Cao X, van den Hil FE, Mummery CL, Orlova VV
Generation and Functional Characterization of Monocytes and Macrophages Derived from Human Induced Pluripotent Stem Cells
Cao X et al. Generation and Functional Characterization of Monocytes and Macrophages Derived from Human Induced Pluripotent Stem Cells. . 2020-03-00. Pubmed ID: 32159928; DOI: 10.1002/cpsc.108; PMC: PMC7154707 LUMCi001-A 2020-03-00 2020-03-00 PubMed: 32159928 DOI: 10.1002/cpsc.108Associated cell lines:
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Laowtammathron C, Chingsuwanrote P, Choavaratana R, Phornwilardsiri S, Sitthirit K, Kaewjunun C, Makemaharn O, Terbto P, Waeteekul S, Lorthongpanich C, U-Pratya Y, Srisook P, Kheolamai P, Issaragrisil S
Derivation of human embryonic stem cell line MUSIe001-A from an embryo with homozygous α(0)-thalassemia (SEA deletion)
Laowtammathron C et al. Derivation of human embryonic stem cell line MUSIe001-A from an embryo with homozygous α(0)-thalassemia (SEA deletion). . 2020-03-00. Pubmed ID: 31945613; DOI: 10.1016/j.scr.2019.101695 MUSIe001-A 2020-03-00 2020-03-00 PubMed: 31945613 DOI: 10.1016/j.scr.2019.101695Associated cell lines:
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Park H, Han J, Lee Y, Kwak S, Koo SK
Generation of a human induced pluripotent stem cell line from a patient with Leber congenital amaurosis
Park H et al. Generation of a human induced pluripotent stem cell line from a patient with Leber congenital amaurosis. . 2020-03-00. Pubmed ID: 32036247; DOI: 10.1016/j.scr.2020.101725 KSCBi011-A 2020-03-00 2020-03-00 PubMed: 32036247 DOI: 10.1016/j.scr.2020.101725Associated cell lines:
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Ma Y, Zhang H, Li X, Yang X, Li Y, Guan J, Lv Y, Gai Z, Liu Y
An integration-free iPSC line (SDQLCHi017-A) derived from a patient with nemaline myopathy-2 disease carrying compound heterozygote mutations in NEB gene
Ma Y et al. An integration-free iPSC line (SDQLCHi017-A) derived from a patient with nemaline myopathy-2 disease carrying compound heterozygote mutations in NEB gene. . 2020-03-00. Pubmed ID: 32062132; DOI: 10.1016/j.scr.2020.101729 SDQLCHi017-A 2020-03-00 2020-03-00 PubMed: 32062132 DOI: 10.1016/j.scr.2020.101729Associated cell lines:
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Castro-Viñuelas R, Sanjurjo-Rodríguez C, Piñeiro-Ramil M, Rodríguez-Fernández S, Fuentes-Boquete IM, Blanco FJ, Díaz-Prado SM
Generation of a human control iPS cell line (ESi080-A) from a donor with no rheumatic diseases
Castro-Viñuelas R et al. Generation of a human control iPS cell line (ESi080-A) from a donor with no rheumatic diseases. . 2020-03-00. Pubmed ID: 31962233; DOI: 10.1016/j.scr.2019.101683 ESi080-A 2020-03-00 2020-03-00 PubMed: 31962233 DOI: 10.1016/j.scr.2019.101683Associated cell lines:
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Klauzen P, Perepelina K, Khudiakov A, Zlotina A, Fomicheva Y, Pervunina T, Vershinina T, Kostareva A, Malashicheva A
Generation of two induced pluripotent stem cell lines (FAMRCi005-A and FAMRCi005-B) from patient carrying genetic variant LMNA p.Asp357Val
Klauzen P et al. Generation of two induced pluripotent stem cell lines (FAMRCi005-A and FAMRCi005-B) from patient carrying genetic variant LMNA p.Asp357Val. . 2020-03-00. Pubmed ID: 32062135; DOI: 10.1016/j.scr.2020.101719 FAMRCi005-AFAMRCi005-B 2020-03-00 2020-03-00 PubMed: 32062135 DOI: 10.1016/j.scr.2020.101719Associated cell lines:
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Przepiorski A, Crunk AE, Espiritu EB, Hukriede NA, Davidson AJ
The Utility of Human Kidney Organoids in Modeling Kidney Disease
Przepiorski A et al. The Utility of Human Kidney Organoids in Modeling Kidney Disease. . 2020-03-00. Pubmed ID: 32303281; DOI: 10.1016/j.semnephrol.2020.01.009; PMC: PMC9003567 BCRTi004-ABCRTi005-A 2020-03-00 2020-03-00 PubMed: 32303281 DOI: 10.1016/j.semnephrol.2020.01.009Associated cell lines:
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Haake K, Wüstefeld T, Merkert S, Lüttge D, Göhring G, Auber B, Baumann U, Lachmann N
Human STAT1 gain-of-function iPSC line from a patient suffering from chronic mucocutaneous candidiasis
Haake K et al. Human STAT1 gain-of-function iPSC line from a patient suffering from chronic mucocutaneous candidiasis. . 2020-03-00. Pubmed ID: 32000109; DOI: 10.1016/j.scr.2020.101713 MHHi010-A 2020-03-00 2020-03-00 PubMed: 32000109 DOI: 10.1016/j.scr.2020.101713Associated cell lines:
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Li X, Liu Y, Liu F, Wang X, Liu M, Du W, Zhao J, Wang M, Hu L, Wang C, Fu W, Dong J, Zhao X
Generation of a hiPSC line ZZUNEUi007-A from a patient with hypertrophic cardiomyopathy caused by mutation in MYH7
Li X et al. Generation of a hiPSC line ZZUNEUi007-A from a patient with hypertrophic cardiomyopathy caused by mutation in MYH7. . 2020-03-00. Pubmed ID: 31931472; DOI: 10.1016/j.scr.2020.101699 ZZUNEUi007-A 2020-03-00 2020-03-00 PubMed: 31931472 DOI: 10.1016/j.scr.2020.101699Associated cell lines:
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Yang X, Yan B, Zhang H, Ma Y, Zhou Q, Li Y, Guan J, Wang D, Liu Y, Gai Z
Generation of an induced pluripotent stem cell line (SDQLCHi009-A) from a patient with 47,XXY and ornithine transcarbamylase deficiency carrying a hemizygote mutation in OTC
Yang X et al. Generation of an induced pluripotent stem cell line (SDQLCHi009-A) from a patient with 47,XXY and ornithine transcarbamylase deficiency carrying a hemizygote mutation in OTC. . 2020-03-00. Pubmed ID: 32014801; DOI: 10.1016/j.scr.2020.101704 SDQLCHi009-A 2020-03-00 2020-03-00 PubMed: 32014801 DOI: 10.1016/j.scr.2020.101704Associated cell lines:
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Gao Y, Wang Y, Wang Z, Sun H, Zhang R, Yang J, Liu Y, Liu H, Zhang Q, Zhang S, Shi C, Xu Y, Song B
Generation of induced pluripotent stem cell line (ZZUi0016-A) from dermal fibroblasts of a normal human
Gao Y et al. Generation of induced pluripotent stem cell line (ZZUi0016-A) from dermal fibroblasts of a normal human. . 2020-03-00. Pubmed ID: 32007761; DOI: 10.1016/j.scr.2020.101717 ZZUi016-AZZUi037-A 2020-03-00 2020-03-00 PubMed: 32007761 DOI: 10.1016/j.scr.2020.101717 -
Perepelina K, Klauzen P, Khudiakov A, Zlotina A, Fomicheva Y, Rudenko D, Gordeev M, Sergushichev A, Malashicheva A, Kostareva A
Generation of two iPSC lines (FAMRCi006-A and FAMRCi006-B) from patient with dilated cardiomyopathy and Emery-Dreifuss muscular dystrophy associated with genetic variant LMNAp.Arg527Pro
Perepelina K et al. Generation of two iPSC lines (FAMRCi006-A and FAMRCi006-B) from patient with dilated cardiomyopathy and Emery-Dreifuss muscular dystrophy associated with genetic variant LMNAp.Arg527Pro. . 2020-03-00. Pubmed ID: 32059175; DOI: 10.1016/j.scr.2020.101714 FAMRCi006-AFAMRCi006-B 2020-03-00 2020-03-00 PubMed: 32059175 DOI: 10.1016/j.scr.2020.101714Associated cell lines:
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Petters J, Cimmaruta C, Iwanov K, Chang ML, Völkner C, Knuebel G, Murua Escobar H, Frech MJ, Hermann A, Rolfs A, Lukas J
Generation of induced pluripotent stem cell lines AKOSi002-A and AKOSi003-A from symptomatic female adults with Wilson disease
Petters J et al. Generation of induced pluripotent stem cell lines AKOSi002-A and AKOSi003-A from symptomatic female adults with Wilson disease. . 2020-03-00. Pubmed ID: 32028086; DOI: 10.1016/j.scr.2020.101708 AKOSi002-AAKOSi003-A 2020-03-00 2020-03-00 PubMed: 32028086 DOI: 10.1016/j.scr.2020.101708Associated cell lines:
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Korshunova I, Rhein S, García-González D, Stölting I, Pfisterer U, Barta A, Dmytriyeva O, Kirkeby A, Schwaninger M, Khodosevich K
Genetic modification increases the survival and the neuroregenerative properties of transplanted neural stem cells
Korshunova I et al. Genetic modification increases the survival and the neuroregenerative properties of transplanted neural stem cells. . 2020-02-27. Pubmed ID: 31999645; DOI: 10.1172/jci.insight.126268; PMC: PMC7101138 WAe009-ARCe021-A 2020-02-27 2020-02-27 PubMed: 31999645 DOI: 10.1172/jci.insight.126268 -
Claus C, Jung M, Hübschen JM
Pluripotent Stem Cell-Based Models: A Peephole into Virus Infections during Early Pregnancy
Claus C et al. Pluripotent Stem Cell-Based Models: A Peephole into Virus Infections during Early Pregnancy. . 2020-02-26. Pubmed ID: 32110999; DOI: 10.3390/cells9030542; PMC: PMC7140399 WISCi004-B 2020-02-26 2020-02-26 PubMed: 32110999 DOI: 10.3390/cells9030542Associated cell lines:
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Pará C, Bose P, Pshezhetsky AV
Neuropathophysiology of Lysosomal Storage Diseases: Synaptic Dysfunction as a Starting Point for Disease Progression
Pará C et al. Neuropathophysiology of Lysosomal Storage Diseases: Synaptic Dysfunction as a Starting Point for Disease Progression. . 2020-02-25. Pubmed ID: 32106459; DOI: 10.3390/jcm9030616; PMC: PMC7141115 INSAi001-A 2020-02-25 2020-02-25 PubMed: 32106459 DOI: 10.3390/jcm9030616Associated cell lines:
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Ke M, Chong CM, Zeng H, Huang M, Huang Z, Zhang K, Cen X, Lu JH, Yao X, Qin D, Su H
Azoramide protects iPSC-derived dopaminergic neurons with PLA2G6 D331Y mutation through restoring ER function and CREB signaling
Ke M et al. Azoramide protects iPSC-derived dopaminergic neurons with PLA2G6 D331Y mutation through restoring ER function and CREB signaling. . 2020-02-18. Pubmed ID: 32071291; DOI: 10.1038/s41419-020-2312-8; PMC: PMC7028918 IBMSi012-A 2020-02-18 2020-02-18 PubMed: 32071291 DOI: 10.1038/s41419-020-2312-8Associated cell lines:
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D'Avanzo F, Rigon L, Zanetti A, Tomanin R
Mucopolysaccharidosis Type II: One Hundred Years of Research, Diagnosis, and Treatment
D'Avanzo F et al. Mucopolysaccharidosis Type II: One Hundred Years of Research, Diagnosis, and Treatment. . 2020-02-13. Pubmed ID: 32070051; DOI: 10.3390/ijms21041258; PMC: PMC7072947 TRNDi008-A 2020-02-13 2020-02-13 PubMed: 32070051 DOI: 10.3390/ijms21041258Associated cell lines:
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Saleem U, Mannhardt I, Braren I, Denning C, Eschenhagen T, Hansen A
Force and Calcium Transients Analysis in Human Engineered Heart Tissues Reveals Positive Force-Frequency Relation at Physiological Frequency
Saleem U et al. Force and Calcium Transients Analysis in Human Engineered Heart Tissues Reveals Positive Force-Frequency Relation at Physiological Frequency. . 2020-02-11. Pubmed ID: 31956082; DOI: 10.1016/j.stemcr.2019.12.011; PMC: PMC7013237 UKEi001-AUKEi003-C 2020-02-11 2020-02-11 PubMed: 31956082 DOI: 10.1016/j.stemcr.2019.12.011 -
Choi IY, Lim H, Cho HJ, Oh Y, Chou BK, Bai H, Cheng L, Kim YJ, Hyun S, Kim H, Shin JH, Lee G
Transcriptional landscape of myogenesis from human pluripotent stem cells reveals a key role of TWIST1 in maintenance of skeletal muscle progenitors
Choi IY et al. Transcriptional landscape of myogenesis from human pluripotent stem cells reveals a key role of TWIST1 in maintenance of skeletal muscle progenitors. . 2020-02-03. Pubmed ID: 32011235; DOI: 10.7554/elife.46981; PMC: PMC6996923 WAe009-A 2020-02-03 2020-02-03 PubMed: 32011235 DOI: 10.7554/elife.46981Associated cell lines:
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Pearse Y, Iacovino M
A Cure for Sanfilippo Syndrome? A Summary of Current Therapeutic Approaches and their Promise
Pearse Y et al. A Cure for Sanfilippo Syndrome? A Summary of Current Therapeutic Approaches and their Promise. . 2020-02-01. Pubmed ID: 32733997; DOI: 10.18103/mra.v8i2.2045; PMC: PMC7391468 IMEDEAi004-AIMEDEAi004-B 2020-02-01 2020-02-01 PubMed: 32733997 DOI: 10.18103/mra.v8i2.2045Associated cell lines:
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McLoughlin HS, Moore LR, Paulson HL
Pathogenesis of SCA3 and implications for other polyglutamine diseases
McLoughlin HS et al. Pathogenesis of SCA3 and implications for other polyglutamine diseases. . 2020-02-00. Pubmed ID: 31669734; DOI: 10.1016/j.nbd.2019.104635; PMC: PMC6980715 MUSIi004-A 2020-02-00 2020-02-00 PubMed: 31669734 DOI: 10.1016/j.nbd.2019.104635Associated cell lines:
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Moretti A, Fonteyne L, Giesert F, Hoppmann P, Meier AB, Bozoglu T, Baehr A, Schneider CM, Sinnecker D, Klett K, Fröhlich T, Rahman FA, Haufe T, Sun S, Jurisch V, Kessler B, Hinkel R, Dirschinger R, Martens E, Jilek C, Graf A, Krebs S, Santamaria G, Kurome M, Zakhartchenko V, Campbell B, Voelse K, Wolf A, Ziegler T, Reichert S, Lee S, Flenkenthaler F, Dorn T, Jeremias I, Blum H, Dendorfer A, Schnieke A, Krause S, Walter MC, Klymiuk N, Laugwitz KL, Wolf E, Wurst W, Kupatt C
Somatic gene editing ameliorates skeletal and cardiac muscle failure in pig and human models of Duchenne muscular dystrophy
Moretti A et al. Somatic gene editing ameliorates skeletal and cardiac muscle failure in pig and human models of Duchenne muscular dystrophy. . 2020-02-00. Pubmed ID: 31988462; DOI: 10.1038/s41591-019-0738-2; PMC: PMC7212064 MRIi027-A-1 2020-02-00 2020-02-00 PubMed: 31988462 DOI: 10.1038/s41591-019-0738-2Associated cell lines:
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Do HS, Park SW, Im I, Seo D, Yoo HW, Go H, Kim YH, Koh GY, Lee BH, Han YM
Enhanced thrombospondin-1 causes dysfunction of vascular endothelial cells derived from Fabry disease-induced pluripotent stem cells
Do HS et al. Enhanced thrombospondin-1 causes dysfunction of vascular endothelial cells derived from Fabry disease-induced pluripotent stem cells. . 2020-02-00. Pubmed ID: 31981984; DOI: 10.1016/j.ebiom.2020.102633; PMC: PMC6992938 DDLABi001-A 2020-02-00 2020-02-00 PubMed: 31981984 DOI: 10.1016/j.ebiom.2020.102633Associated cell lines:
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Sung TC, Li HF, Higuchi A, Kumar SS, Ling QD, Wu YW, Burnouf T, Nasu M, Umezawa A, Lee KF, Wang HC, Chang Y, Hsu ST
Effect of cell culture biomaterials for completely xeno-free generation of human induced pluripotent stem cells
Sung TC et al. Effect of cell culture biomaterials for completely xeno-free generation of human induced pluripotent stem cells. . 2020-02-00. Pubmed ID: 31810728; DOI: 10.1016/j.biomaterials.2019.119638 GPCCi001-A 2020-02-00 2020-02-00 PubMed: 31810728 DOI: 10.1016/j.biomaterials.2019.119638Associated cell lines:
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Ben M'Barek K, Bertin S, Brazhnikova E, Jaillard C, Habeler W, Plancheron A, Fovet CM, Demilly J, Jarraya M, Bejanariu A, Sahel JA, Peschanski M, Goureau O, Monville C
Clinical-grade production and safe delivery of human ESC derived RPE sheets in primates and rodents
Ben M'Barek K et al. Clinical-grade production and safe delivery of human ESC derived RPE sheets in primates and rodents. . 2020-02-00. Pubmed ID: 31732225; DOI: 10.1016/j.biomaterials.2019.119603 RCe013-A 2020-02-00 2020-02-00 PubMed: 31732225 DOI: 10.1016/j.biomaterials.2019.119603Associated cell lines:
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Liu G, David BT, Trawczynski M, Fessler RG
Advances in Pluripotent Stem Cells: History, Mechanisms, Technologies, and Applications
Liu G et al. Advances in Pluripotent Stem Cells: History, Mechanisms, Technologies, and Applications. . 2020-02-00. Pubmed ID: 31760627; DOI: 10.1007/s12015-019-09935-x; PMC: PMC6987053 ZZUi004-AZZUi011-A 2020-02-00 2020-02-00 PubMed: 31760627 DOI: 10.1007/s12015-019-09935-x -
Vélez JI, Lopera F, Silva CT, Villegas A, Espinosa LG, Vidal OM, Mastronardi CA, Arcos-Burgos M
Familial Alzheimer's Disease and Recessive Modifiers
Vélez JI et al. Familial Alzheimer's Disease and Recessive Modifiers. . 2020-02-00. Pubmed ID: 31664702; DOI: 10.1007/s12035-019-01798-0; PMC: PMC7031188 IMEDEAi006-A 2020-02-00 2020-02-00 PubMed: 31664702 DOI: 10.1007/s12035-019-01798-0Associated cell lines:
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Piers TM, Cosker K, Mallach A, Johnson GT, Guerreiro R, Hardy J, Pocock JM
A locked immunometabolic switch underlies TREM2 R47H loss of function in human iPSC-derived microglia
Piers TM et al. A locked immunometabolic switch underlies TREM2 R47H loss of function in human iPSC-derived microglia. . 2020-02-00. Pubmed ID: 31907987; DOI: 10.1096/fj.201902447r; PMC: PMC7027848 BIONi010-C 2020-02-00 2020-02-00 PubMed: 31907987 DOI: 10.1096/fj.201902447rAssociated cell lines:
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Pölönen RP, Swan H, Aalto-Setälä K
Mutation-specific differences in arrhythmias and drug responses in CPVT patients: simultaneous patch clamp and video imaging of iPSC derived cardiomyocytes
Pölönen RP et al. Mutation-specific differences in arrhythmias and drug responses in CPVT patients: simultaneous patch clamp and video imaging of iPSC derived cardiomyocytes. . 2020-02-00. Pubmed ID: 31786768; DOI: 10.1007/s11033-019-05201-y TAUi002-A 2020-02-00 2020-02-00 PubMed: 31786768 DOI: 10.1007/s11033-019-05201-yAssociated cell lines:
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Hu T, Yao B, Huang S, Fu X
Insight into cellular dedifferentiation in regenerative medicine
Hu T et al. Insight into cellular dedifferentiation in regenerative medicine. . 2020-02-00. Pubmed ID: 31187305; DOI: 10.1007/s11427-019-9571-y ISMMSi002-BZZUi003-AIISHDOi001-A 2020-02-00 2020-02-00 PubMed: 31187305 DOI: 10.1007/s11427-019-9571-yAssociated cell lines:
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Ast J, Arvaniti A, Fine NHF, Nasteska D, Ashford FB, Stamataki Z, Koszegi Z, Bacon A, Jones BJ, Lucey MA, Sasaki S, Brierley DI, Hastoy B, Tomas A, D'Agostino G, Reimann F, Lynn FC, Reissaus CA, Linnemann AK, D'Este E, Calebiro D, Trapp S, Johnsson K, Podewin T, Broichhagen J, Hodson DJ
Super-resolution microscopy compatible fluorescent probes reveal endogenous glucagon-like peptide-1 receptor distribution and dynamics
Ast J et al. Super-resolution microscopy compatible fluorescent probes reveal endogenous glucagon-like peptide-1 receptor distribution and dynamics. . 2020-01-24. Pubmed ID: 31980626; DOI: 10.1038/s41467-020-14309-w; PMC: PMC6981144 WAe001-A 2020-01-24 2020-01-24 PubMed: 31980626 DOI: 10.1038/s41467-020-14309-wAssociated cell lines:
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Satir TM, Nazir FH, Vizlin-Hodzic D, Hardselius E, Blennow K, Wray S, Zetterberg H, Agholme L, Bergström P
Accelerated neuronal and synaptic maturation by BrainPhys medium increases Aβ secretion and alters Aβ peptide ratios from iPSC-derived cortical neurons
Satir TM et al. Accelerated neuronal and synaptic maturation by BrainPhys medium increases Aβ secretion and alters Aβ peptide ratios from iPSC-derived cortical neurons. . 2020-01-17. Pubmed ID: 31953468; DOI: 10.1038/s41598-020-57516-7; PMC: PMC6969066 WTSIi015-A 2020-01-17 2020-01-17 PubMed: 31953468 DOI: 10.1038/s41598-020-57516-7Associated cell lines:
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Assou S, Girault N, Plinet M, Bouckenheimer J, Sansac C, Combe M, Mianné J, Bourguignon C, Fieldes M, Ahmed E, Commes T, Boureux A, Lemaître JM, De Vos J
Recurrent Genetic Abnormalities in Human Pluripotent Stem Cells: Definition and Routine Detection in Culture Supernatant by Targeted Droplet Digital PCR
Assou S et al. Recurrent Genetic Abnormalities in Human Pluripotent Stem Cells: Definition and Routine Detection in Culture Supernatant by Targeted Droplet Digital PCR. . 2020-01-14. Pubmed ID: 31902703; DOI: 10.1016/j.stemcr.2019.12.004; PMC: PMC6962701 UHOMi001-A 2020-01-14 2020-01-14 PubMed: 31902703 DOI: 10.1016/j.stemcr.2019.12.004Associated cell lines:
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Vázquez-Vélez GE, Gonzales KA, Revelli JP, Adamski CJ, Alavi Naini F, Bajić A, Craigen E, Richman R, Heman-Ackah SM, Wood MJA, Rousseaux MWC, Zoghbi HY
Doublecortin-like Kinase 1 Regulates α-Synuclein Levels and Toxicity
Vázquez-Vélez GE et al. Doublecortin-like Kinase 1 Regulates α-Synuclein Levels and Toxicity. . 2020-01-08. Pubmed ID: 31748376; DOI: 10.1523/jneurosci.1076-19.2019; PMC: PMC6948939 WAe009-A 2020-01-08 2020-01-08 PubMed: 31748376 DOI: 10.1523/jneurosci.1076-19.2019Associated cell lines:
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Bai Y, Zhu C, Feng M, Pan B, Zhang S, Zhan X, Chen H, Wang B, Li J
Establishment of A Reversibly Inducible Porcine Granulosa Cell Line
Bai Y et al. Establishment of A Reversibly Inducible Porcine Granulosa Cell Line. . 2020-01-08. Pubmed ID: 31936362; DOI: 10.3390/cells9010156; PMC: PMC7017277 NERCe002-ANERCe002-A-3 2020-01-08 2020-01-08 PubMed: 31936362 DOI: 10.3390/cells9010156Associated cell lines:
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Chen L, Wang Y, Xie J.
A Human iPSC Line Carrying a de novo Pathogenic FUS Mutation Identified in a Patient With Juvenile ALS Differentiated Into Motor Neurons With Pathological Characteristics
Chen L et al. A Human iPSC Line Carrying a de novo Pathogenic FUS Mutation Identified in a Patient With Juvenile ALS Differentiated Into Motor Neurons With Pathological Characteristics. . 2020-01-01. ZZUNEUi010-A 2020-01-01 2020-01-01Associated cell lines:
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Reich M, Paris I, Ebeling M, Dahm N, Schweitzer C, Reinhardt D, Schmucki R, Prasad M, Köchl F, Leist M, Cowley S, Zhang J, Patsch C, Gutbier S, Britschgi M.
Alzheimer’s Risk Gene TREM2 Determines Functional Properties of New Type of Human iPSC-Derived Microglia
Reich M et al. Alzheimer’s Risk Gene TREM2 Determines Functional Properties of New Type of Human iPSC-Derived Microglia. . 2020-01-01. BIONi010-C 2020-01-01 2020-01-01Associated cell lines:
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Hall-Roberts H, Agarwal D, Obst J, Smith T, Monzón-Sandoval J, Di Daniel E, Webber C, James W, Mead E, Davis J, Cowley S.
TREM2 Alzheimer’s variant R47H causes similar transcriptional dysregulation to knockout, yet only subtle functional phenotypes in human iPSC-derived macrophages
Hall-Roberts H et al. TREM2 Alzheimer’s variant R47H causes similar transcriptional dysregulation to knockout, yet only subtle functional phenotypes in human iPSC-derived macrophages. . 2020-01-01. BIONi010-C-7 2020-01-01 2020-01-01Associated cell lines:
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Xiao C, Yu M, Liu J, Wu H, Deng M, Zhang Q, Xiao X
Generation of an integration-free induced pluripotent stem cell line (PUMCHi001-A) from a patient with familial partial lipodystrophy type 2 (FPLD2) carrying a heterozygous p.R349W (c.1045C > T) mutation in the LMNA gene
Xiao C et al. Generation of an integration-free induced pluripotent stem cell line (PUMCHi001-A) from a patient with familial partial lipodystrophy type 2 (FPLD2) carrying a heterozygous p.R349W (c.1045C > T) mutation in the LMNA gene. . 2020-01-00. Pubmed ID: 31794942; DOI: 10.1016/j.scr.2019.101651 PUMCHi001-A 2020-01-00 2020-01-00 PubMed: 31794942 DOI: 10.1016/j.scr.2019.101651Associated cell lines:
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Mura M, Bastaroli F, Corli M, Ginevrino M, Calabrò F, Boni M, Crotti L, Valente EM, Schwartz PJ, Gnecchi M
Generation of the human induced pluripotent stem cell (hiPSC) line PSMi006-A from a patient affected by an autosomal recessive form of long QT syndrome type 1
Mura M et al. Generation of the human induced pluripotent stem cell (hiPSC) line PSMi006-A from a patient affected by an autosomal recessive form of long QT syndrome type 1. . 2020-01-00. Pubmed ID: 31785541; DOI: 10.1016/j.scr.2019.101658 PSMi006-A 2020-01-00 2020-01-00 PubMed: 31785541 DOI: 10.1016/j.scr.2019.101658Associated cell lines:
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Tannenbaum SE, Singer O, Gil Y, Berman-Zaken Y, Ilouz N, Khaner H, Haimov M, Reubinoff BE
Hadassah, provider of "Regulatory-Ready" pluripotent clinical-grade stem cell banks
Tannenbaum SE et al. Hadassah, provider of "Regulatory-Ready" pluripotent clinical-grade stem cell banks. . 2020-01-00. Pubmed ID: 31838378; DOI: 10.1016/j.scr.2019.101670 HADe008-AHADe009-AHADe010-AHADe011-AHADe012-AHADe013-AHADe007-BHADe008-BHADe009-BHADe007-C 2020-01-00 2020-01-00 PubMed: 31838378 DOI: 10.1016/j.scr.2019.101670 -
Lanzi G, Ferraro RM, Masneri S, Piovani G, Barisani C, Sobacchi C, Villa A, Vezzoni P, Giliani S
Generation of 3 clones of induced pluripotent stem cells (iPSCs) from a patient affected by Autosomal Recessive Osteopetrosis due to mutations in TCIRG1 gene
Lanzi G et al. Generation of 3 clones of induced pluripotent stem cells (iPSCs) from a patient affected by Autosomal Recessive Osteopetrosis due to mutations in TCIRG1 gene. . 2020-01-00. Pubmed ID: 31794943; DOI: 10.1016/j.scr.2019.101660 UNIBSi010-AUNIBSi010-BUNIBSi010-C 2020-01-00 2020-01-00 PubMed: 31794943 DOI: 10.1016/j.scr.2019.101660Associated cell lines:
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Ma J, Zhang J, He J, Zhang Z, Li W, Feng B, Guo R, Amponsah AE, Kong D, Liu A, Song Y, Wei L, Cui H
Induced pluripotent stem cell (iPSC) line (HEBHMUi002-A) from a healthy female individual and neural differentiation
Ma J et al. Induced pluripotent stem cell (iPSC) line (HEBHMUi002-A) from a healthy female individual and neural differentiation. . 2020-01-00. Pubmed ID: 31791011; DOI: 10.1016/j.scr.2019.101669 DHMCi005-AHEBHMUi002-A 2020-01-00 2020-01-00 PubMed: 31791011 DOI: 10.1016/j.scr.2019.101669Associated cell lines:
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Rodríguez-Traver E, Díaz-Guerra E, Rodríguez C, Arenas F, Orera M, Kulisevsky J, Moratalla R, Vicario C
A collection of three integration-free iPSCs derived from old male and female healthy subjects
Rodríguez-Traver E et al. A collection of three integration-free iPSCs derived from old male and female healthy subjects. . 2020-01-00. Pubmed ID: 31794941; DOI: 10.1016/j.scr.2019.101663 ICCSICi012-AICCSICi013-AICCSICi014-A 2020-01-00 2020-01-00 PubMed: 31794941 DOI: 10.1016/j.scr.2019.101663Associated cell lines:
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Ustyantseva EI, Medvedev SP, Vetchinova AS, Illarioshkin SN, Leonov SV, Zakian SM
Generation of an induced pluripotent stem cell line, ICGi014-A, by reprogramming peripheral blood mononuclear cells from a patient with homozygous D90A mutation in SOD1 causing Amyotrophic lateral sclerosis
Ustyantseva EI et al. Generation of an induced pluripotent stem cell line, ICGi014-A, by reprogramming peripheral blood mononuclear cells from a patient with homozygous D90A mutation in SOD1 causing Amyotrophic lateral sclerosis. . 2020-01-00. Pubmed ID: 31830646; DOI: 10.1016/j.scr.2019.101675 ICGi014-A 2020-01-00 2020-01-00 PubMed: 31830646 DOI: 10.1016/j.scr.2019.101675Associated cell lines:
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Patterson K, Linask KL, Beers J, Zou J
Generation of two tdTomato reporter induced pluripotent stem cell lines (NHLBIi003-A-1 and NHLBIi003-A-2) by AAVS1 safe harbor gene-editing
Patterson K et al. Generation of two tdTomato reporter induced pluripotent stem cell lines (NHLBIi003-A-1 and NHLBIi003-A-2) by AAVS1 safe harbor gene-editing. . 2020-01-00. Pubmed ID: 31869686; DOI: 10.1016/j.scr.2019.101673; PMC: PMC7046126 TRNDi008-ANHLBIi003-ANHLBIi003-A-1NHLBIi003-A-2 2020-01-00 2020-01-00 PubMed: 31869686 DOI: 10.1016/j.scr.2019.101673Associated cell lines:
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Drick N, Sahabian A, Pongpamorn P, Merkert S, Göhring G, Welte T, Martin U, Olmer R
Generation of a NKX2.1 - p63 double transgenic knock-in reporter cell line from human induced pluripotent stem cells (MHHi006-A-4)
Drick N et al. Generation of a NKX2.1 - p63 double transgenic knock-in reporter cell line from human induced pluripotent stem cells (MHHi006-A-4). . 2020-01-00. Pubmed ID: 31791010; DOI: 10.1016/j.scr.2019.101659 MHHi006-AMHHi006-A-2MHHi006-A-4 2020-01-00 2020-01-00 PubMed: 31791010 DOI: 10.1016/j.scr.2019.101659Associated cell lines:
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Balez R, Berg T, Bax M, Muñoz SS, Cabral-da-Silva MC, Engel M, Do-Ha D, Stevens CH, Rowe D, Yang S, Blair IP, Ooi L
The mRNA-based reprogramming of fibroblasts from a SOD1(E101G) familial amyotrophic lateral sclerosis patient to induced pluripotent stem cell line UOWi007
Balez R et al. The mRNA-based reprogramming of fibroblasts from a SOD1(E101G) familial amyotrophic lateral sclerosis patient to induced pluripotent stem cell line UOWi007. . 2020-01-00. Pubmed ID: 32006803; DOI: 10.1016/j.scr.2020.101701 UOWi007-A 2020-01-00 2020-01-00 PubMed: 32006803 DOI: 10.1016/j.scr.2020.101701Associated cell lines:
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Thayer JA, Awad O, Hegdekar N, Sarkar C, Tesfay H, Burt C, Zeng X, Feldman RA, Lipinski MM
The PARK10 gene USP24 is a negative regulator of autophagy and ULK1 protein stability
Thayer JA et al. The PARK10 gene USP24 is a negative regulator of autophagy and ULK1 protein stability. . 2020-01-00. Pubmed ID: 30957634; DOI: 10.1080/15548627.2019.1598754; PMC: PMC6984603 CRMi003-A-1 2020-01-00 2020-01-00 PubMed: 30957634 DOI: 10.1080/15548627.2019.1598754Associated cell lines:
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Han S, Zhang YY, Meng MY, Hou ZL, Meng P, Zhao YY, Gao H, Tang J, Liu Z, Yang LL, Jiang LH, Li YX
Generation of human iPSC line from a patient with Tetralogy of Fallot, YAHKMUi001-A, carrying a mutation in TBX1 gene
Han S et al. Generation of human iPSC line from a patient with Tetralogy of Fallot, YAHKMUi001-A, carrying a mutation in TBX1 gene. . 2020-01-00. Pubmed ID: 31869684; DOI: 10.1016/j.scr.2019.101687 YAHKMUi001-A 2020-01-00 2020-01-00 PubMed: 31869684 DOI: 10.1016/j.scr.2019.101687Associated cell lines:
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Wang X, Xie S, Li Z, Ye Z, Gu X, Zhou L, Li H
Generation of an iPSC line (HUSTi002-A) from fibroblasts of a patient with Sertoli cell-only syndrome carrying c.731_732delAT in PIWIL2 gene
Wang X et al. Generation of an iPSC line (HUSTi002-A) from fibroblasts of a patient with Sertoli cell-only syndrome carrying c.731_732delAT in PIWIL2 gene. . 2020-01-00. Pubmed ID: 32006804; DOI: 10.1016/j.scr.2020.101703 HUSTi002-A 2020-01-00 2020-01-00 PubMed: 32006804 DOI: 10.1016/j.scr.2020.101703Associated cell lines:
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Lu HE, Tsai CL, Chiu IM, Pan YL, Lin YF, Lin HC, Hsu YC
Generation of induced pluripotent stem cells MMCi001-A from a Taiwanese hearing loss patient carrying GJB2 pV37I mutation
Lu HE et al. Generation of induced pluripotent stem cells MMCi001-A from a Taiwanese hearing loss patient carrying GJB2 pV37I mutation. . 2020-01-00. Pubmed ID: 31896484; DOI: 10.1016/j.scr.2019.101692 MMCi001-A 2020-01-00 2020-01-00 PubMed: 31896484 DOI: 10.1016/j.scr.2019.101692Associated cell lines:
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Benetó N, Cozar M, Gort L, Pacheco L, Vilageliu L, Grinberg D, Canals I
Generation of two NAGLU-mutated homozygous cell lines from healthy induced pluripotent stem cells using CRISPR/Cas9 to model Sanfilippo B syndrome
Benetó N et al. Generation of two NAGLU-mutated homozygous cell lines from healthy induced pluripotent stem cells using CRISPR/Cas9 to model Sanfilippo B syndrome. . 2020-01-00. Pubmed ID: 31825816; DOI: 10.1016/j.scr.2019.101668 UBi001-AUBi001-A-3UBi001-A-4 2020-01-00 2020-01-00 PubMed: 31825816 DOI: 10.1016/j.scr.2019.101668Associated cell lines:
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Kim YK, Yu JH, Min SH, Park SW
Generation of a GLA knock-out human-induced pluripotent stem cell line, KSBCi002-A-1, using CRISPR/Cas9
Kim YK et al. Generation of a GLA knock-out human-induced pluripotent stem cell line, KSBCi002-A-1, using CRISPR/Cas9. . 2020-01-00. Pubmed ID: 31841972; DOI: 10.1016/j.scr.2019.101676 KSCBi002-AKSCBi002-A-1 2020-01-00 2020-01-00 PubMed: 31841972 DOI: 10.1016/j.scr.2019.101676Associated cell lines:
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Ma B, Luo M, Yang H, Li T, Liu W, Xu F, Shu C, Chen G, Zhou Z
Generation of a human induced pluripotent stem cell line (NCCDFWi001-A) from a Marfan syndrome patient carrying two FBN1 variants (c.2613A > C and c.684_736 + 4del)
Ma B et al. Generation of a human induced pluripotent stem cell line (NCCDFWi001-A) from a Marfan syndrome patient carrying two FBN1 variants (c.2613A > C and c.684_736 + 4del). . 2020-01-00. Pubmed ID: 31901832; DOI: 10.1016/j.scr.2019.101690 NCCDFWi001-A 2020-01-00 2020-01-00 PubMed: 31901832 DOI: 10.1016/j.scr.2019.101690Associated cell lines:
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Inácio JM, Almeida M, Cristo F, Belo JA
Generation of a gene-corrected human induced pluripotent stem cell line derived from a patient with laterality defects and congenital heart anomalies with a c.455G > A alteration in DAND5
Inácio JM et al. Generation of a gene-corrected human induced pluripotent stem cell line derived from a patient with laterality defects and congenital heart anomalies with a c.455G > A alteration in DAND5. . 2020-01-00. Pubmed ID: 31869685; DOI: 10.1016/j.scr.2019.101677 NMSUNLi001-A 2020-01-00 2020-01-00 PubMed: 31869685 DOI: 10.1016/j.scr.2019.101677Associated cell lines:
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Guan J, Liu X, Zhang H, Yang X, Ma Y, Li Y, Gai Z, Liu Y
Reprogramming of human Peripheral Blood Mononuclear Cell (PBMC) from a Chinese patient suffering Duchenne muscular dystrophy to iPSC line (SDQLCHi007-A) carrying deletion of 49-50 exons in the DMD gene
Guan J et al. Reprogramming of human Peripheral Blood Mononuclear Cell (PBMC) from a Chinese patient suffering Duchenne muscular dystrophy to iPSC line (SDQLCHi007-A) carrying deletion of 49-50 exons in the DMD gene. . 2020-01-00. Pubmed ID: 31812072; DOI: 10.1016/j.scr.2019.101666 SDQLCHi007-A 2020-01-00 2020-01-00 PubMed: 31812072 DOI: 10.1016/j.scr.2019.101666Associated cell lines:
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Fuchs NV, Schieck M, Neuenkirch M, Tondera C, Schmitz H, Steinemann D, Göhring G, König R
Induced pluripotent stem cell line (PEIi003-A) derived from an apparently healthy male individual
Fuchs NV et al. Induced pluripotent stem cell line (PEIi003-A) derived from an apparently healthy male individual. . 2020-01-00. Pubmed ID: 31837633; DOI: 10.1016/j.scr.2019.101679 PEIi001-APEIi003-A 2020-01-00 2020-01-00 PubMed: 31837633 DOI: 10.1016/j.scr.2019.101679 -
Trionfini P, Ciampi O, Romano E, Benigni A, Tomasoni S
Generation of two isogenic knockout PKD2 iPS cell lines, IRFMNi003-A-1 and IRFMNi003-A-2, using CRISPR/Cas9 technology
Trionfini P et al. Generation of two isogenic knockout PKD2 iPS cell lines, IRFMNi003-A-1 and IRFMNi003-A-2, using CRISPR/Cas9 technology. . 2020-01-00. Pubmed ID: 31830647; DOI: 10.1016/j.scr.2019.101667 IRFMNi003-AIRFMNi003-A-1IRFMNi003-A-2IRFMNi001-BIRFMNi001-B-1 2020-01-00 2020-01-00 PubMed: 31830647 DOI: 10.1016/j.scr.2019.101667Associated cell lines:
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Khan M, Vaidyanath A, Suresh D, Vaishnav B, Kakrani AL, Patil S, Shiras A
Generation and characterization of three clones (NCCSi007A, NCCSi007B and NCCSi007C) of an integration free induced Pluripotent Stem Cell line from a patient with alcoholic liver cirrhosis of Indian ethnicity
Khan M et al. Generation and characterization of three clones (NCCSi007A, NCCSi007B and NCCSi007C) of an integration free induced Pluripotent Stem Cell line from a patient with alcoholic liver cirrhosis of Indian ethnicity. . 2020-01-00. Pubmed ID: 31862609; DOI: 10.1016/j.scr.2019.101678 NCCSi007-ANCCSi007-BNCCSi007-C 2020-01-00 2020-01-00 PubMed: 31862609 DOI: 10.1016/j.scr.2019.101678Associated cell lines:
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Elsayed AK, Aghadi M, Ali G, Al-Khawaga S, Hussain K, Abdelalim EM
Generation of a human induced pluripotent stem cell line (QBRIi009-A) from a patient with a heterozygous deletion of FOXA2
Elsayed AK et al. Generation of a human induced pluripotent stem cell line (QBRIi009-A) from a patient with a heterozygous deletion of FOXA2. . 2020-01-00. Pubmed ID: 31991389; DOI: 10.1016/j.scr.2020.101705 QBRIi009-A 2020-01-00 2020-01-00 PubMed: 31991389 DOI: 10.1016/j.scr.2020.101705Associated cell lines:
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Chen M, Maimaitili M, Buchholdt SH, Jensen UB, Febbraro F, Denham M
Generation of eight human induced pluripotent stem cell lines from Parkinson's disease patients carrying familial mutations
Chen M et al. Generation of eight human induced pluripotent stem cell lines from Parkinson's disease patients carrying familial mutations. . 2020-01-00. Pubmed ID: 31786474; DOI: 10.1016/j.scr.2019.101657 DANi002-CDANi003-HDANi004-ADANi005-ADANi006-FDANi007-ADANi008-FDANi009-C 2020-01-00 2020-01-00 PubMed: 31786474 DOI: 10.1016/j.scr.2019.101657 -
Nur Patria Y, Lilianty J, Elefanty AG, Stanley EG, Labonne T, Bateman JF, Lamandé SR
Generation of a SOX9-tdTomato reporter human iPSC line, MCRIi001-A-2, using CRISPR/Cas9 editing
Nur Patria Y et al. Generation of a SOX9-tdTomato reporter human iPSC line, MCRIi001-A-2, using CRISPR/Cas9 editing. . 2020-01-00. Pubmed ID: 31884373; DOI: 10.1016/j.scr.2019.101689 MCRIi001-AMCRIi001-A-2 2020-01-00 2020-01-00 PubMed: 31884373 DOI: 10.1016/j.scr.2019.101689Associated cell lines:
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Prestori F, Moccia F, D'Angelo E
Disrupted Calcium Signaling in Animal Models of Human Spinocerebellar Ataxia (SCA)
Prestori F et al. Disrupted Calcium Signaling in Animal Models of Human Spinocerebellar Ataxia (SCA). . 2019-12-27. Pubmed ID: 31892274; DOI: 10.3390/ijms21010216; PMC: PMC6981692 LUMCi002-ALUMCi003-A 2019-12-27 2019-12-27 PubMed: 31892274 DOI: 10.3390/ijms21010216Associated cell lines:
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Bredenkamp N, Yang J, Clarke J, Stirparo GG, von Meyenn F, Dietmann S, Baker D, Drummond R, Ren Y, Li D, Wu C, Rostovskaya M, Eminli-Meissner S, Smith A, Guo G
Wnt Inhibition Facilitates RNA-Mediated Reprogramming of Human Somatic Cells to Naive Pluripotency
Bredenkamp N et al. Wnt Inhibition Facilitates RNA-Mediated Reprogramming of Human Somatic Cells to Naive Pluripotency. . 2019-12-10. Pubmed ID: 31708477; DOI: 10.1016/j.stemcr.2019.10.009; PMC: PMC6915845 CSCIi001-ACSCIi002-A 2019-12-10 2019-12-10 PubMed: 31708477 DOI: 10.1016/j.stemcr.2019.10.009Associated cell lines:
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Hildebrandt MR, Reuter MS, Wei W, Tayebi N, Liu J, Sharmin S, Mulder J, Lesperance LS, Brauer PM, Mok RSF, Kinnear C, Piekna A, Romm A, Howe J, Pasceri P, Meng G, Rozycki M, Rodrigues DC, Martinez EC, Szego MJ, Zúñiga-Pflücker JC, Anderson MK, Prescott SA, Rosenblum ND, Kamath BM, Mital S, Scherer SW, Ellis J
Precision Health Resource of Control iPSC Lines for Versatile Multilineage Differentiation
Hildebrandt MR et al. Precision Health Resource of Control iPSC Lines for Versatile Multilineage Differentiation. . 2019-12-10. Pubmed ID: 31813827; DOI: 10.1016/j.stemcr.2019.11.003; PMC: PMC6915802 WTSIi013-AWTSIi026-AWTSIi018-BWTSIi046-AWTSIi073-ASKi001-A 2019-12-10 2019-12-10 PubMed: 31813827 DOI: 10.1016/j.stemcr.2019.11.003Associated cell lines:
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Neves KB, Harvey AP, Moreton F, Montezano AC, Rios FJ, Alves-Lopes R, Nguyen Dinh Cat A, Rocchicciolli P, Delles C, Joutel A, Muir K, Touyz RM
ER stress and Rho kinase activation underlie the vasculopathy of CADASIL
Neves KB et al. ER stress and Rho kinase activation underlie the vasculopathy of CADASIL. . 2019-12-05. Pubmed ID: 31647781; DOI: 10.1172/jci.insight.131344; PMC: PMC6962020 IDISi001-A 2019-12-05 2019-12-05 PubMed: 31647781 DOI: 10.1172/jci.insight.131344Associated cell lines:
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Sahabian A, Sgodda M, Naujok O, Dettmer R, Dahlmann J, Manstein F, Cantz T, Zweigerdt R, Martin U, Olmer R
Chemically-Defined, Xeno-Free, Scalable Production of hPSC-Derived Definitive Endoderm Aggregates with Multi-Lineage Differentiation Potential
Sahabian A et al. Chemically-Defined, Xeno-Free, Scalable Production of hPSC-Derived Definitive Endoderm Aggregates with Multi-Lineage Differentiation Potential. . 2019-12-04. Pubmed ID: 31817235; DOI: 10.3390/cells8121571; PMC: PMC6953099 MHHi001-AMHHi006-AMHHi001-A-19 2019-12-04 2019-12-04 PubMed: 31817235 DOI: 10.3390/cells8121571Associated cell lines:
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Bendriem RM, Singh S, Aleem AA, Antonetti DA, Ross ME
Tight junction protein occludin regulates progenitor Self-Renewal and survival in developing cortex
Bendriem RM et al. Tight junction protein occludin regulates progenitor Self-Renewal and survival in developing cortex. . 2019-12-03. Pubmed ID: 31794381; DOI: 10.7554/elife.49376; PMC: PMC6890460 WAe009-A 2019-12-03 2019-12-03 PubMed: 31794381 DOI: 10.7554/elife.49376Associated cell lines:
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Papapetrou EP
Modeling Leukemia with Human Induced Pluripotent Stem Cells
Papapetrou EP. Modeling Leukemia with Human Induced Pluripotent Stem Cells. . 2019-12-02. Pubmed ID: 31451537; DOI: 10.1101/cshperspect.a034868; PMC: PMC6886454 CHOPi001-A 2019-12-02 2019-12-02 PubMed: 31451537 DOI: 10.1101/cshperspect.a034868Associated cell lines:
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Pettingill P, Weir GA, Wei T, Wu Y, Flower G, Lalic T, Handel A, Duggal G, Chintawar S, Cheung J, Arunasalam K, Couper E, Haupt LM, Griffiths LR, Bassett A, Cowley SA, Cader MZ
A causal role for TRESK loss of function in migraine mechanisms
Pettingill P et al. A causal role for TRESK loss of function in migraine mechanisms. . 2019-12-01. Pubmed ID: 31742594; DOI: 10.1093/brain/awz342; PMC: PMC6906598 RCi002-A 2019-12-01 2019-12-01 PubMed: 31742594 DOI: 10.1093/brain/awz342Associated cell lines:
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Hey CAB, Larsen LJ, Tümer Z, Brøndum-Nielsen K, Grønskov K, Hjortshøj TD, Møller LB
Generation and characterization of three isogenic induced pluripotent stem cell lines from a patient with Bardet-Biedl syndrome and homozygous for the BBS5 variant
Hey CAB et al. Generation and characterization of three isogenic induced pluripotent stem cell lines from a patient with Bardet-Biedl syndrome and homozygous for the BBS5 variant. . 2019-12-00. Pubmed ID: 31760295; DOI: 10.1016/j.scr.2019.101594 KCi003-AKCi003-BKCi003-C 2019-12-00 2019-12-00 PubMed: 31760295 DOI: 10.1016/j.scr.2019.101594 -
Leitner D, Ramamoorthy M, Dejosez M, Zwaka TP
Immature mDA neurons ameliorate motor deficits in a 6-OHDA Parkinson's disease mouse model and are functional after cryopreservation
Leitner D et al. Immature mDA neurons ameliorate motor deficits in a 6-OHDA Parkinson's disease mouse model and are functional after cryopreservation. . 2019-12-00. Pubmed ID: 31731178; DOI: 10.1016/j.scr.2019.101617 ISMMSi003-A 2019-12-00 2019-12-00 PubMed: 31731178 DOI: 10.1016/j.scr.2019.101617Associated cell lines:
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Bonilha VL, Bell BA, DeBenedictis MJ, Hagstrom SA, Fishman GA, Hollyfield JG
Cellular Changes in Retinas From Patients With BEST1 Mutations
Bonilha VL et al. Cellular Changes in Retinas From Patients With BEST1 Mutations. . 2020-00-00. Pubmed ID: 33154968; DOI: 10.3389/fcell.2020.573330; PMC: PMC7591587 FRIMOi006-A 2020-00-00 2020-00-00 PubMed: 33154968 DOI: 10.3389/fcell.2020.573330Associated cell lines:
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Zhao M, Chen YJ, Wang MW, Lin XH, Dong EL, Chen WJ, Wang N, Lin X
Genetic and Clinical Profile of Chinese Patients with Autosomal Dominant Spastic Paraplegia
Zhao M et al. Genetic and Clinical Profile of Chinese Patients with Autosomal Dominant Spastic Paraplegia. . 2019-12-00. Pubmed ID: 31630374; DOI: 10.1007/s40291-019-00426-w FJMUi001-A 2019-12-00 2019-12-00 PubMed: 31630374 DOI: 10.1007/s40291-019-00426-wAssociated cell lines:
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Ge N, Liu M, Ding Y, Krawczyk J, McInerney V, Galvin J, Shen S, Prendiville T, O'Brien T
Generation and characterization of twelve human induced pluripotent stem cell (iPSC) lines from four familial long QT syndrome type 1 (LQT1) patients carrying KCNQ1 c.1201dupC mutation
Ge N et al. Generation and characterization of twelve human induced pluripotent stem cell (iPSC) lines from four familial long QT syndrome type 1 (LQT1) patients carrying KCNQ1 c.1201dupC mutation. . 2019-12-00. Pubmed ID: 31765965; DOI: 10.1016/j.scr.2019.101650 NUIGi008-ANUIGi008-BNUIGi008-CNUIGi009-ANUIGi009-BNUIGi009-CNUIGi010-ANUIGi010-BNUIGi010-CNUIGi011-ANUIGi011-BNUIGi011-C 2019-12-00 2019-12-00 PubMed: 31765965 DOI: 10.1016/j.scr.2019.101650Associated cell lines:
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Hayashi Y, Takami M, Matsuo-Takasaki M
Studying Abnormal Chromosomal Diseases Using Patient-Derived Induced Pluripotent Stem Cells
Hayashi Y et al. Studying Abnormal Chromosomal Diseases Using Patient-Derived Induced Pluripotent Stem Cells. . 2020-00-00. Pubmed ID: 32922264; DOI: 10.3389/fncel.2020.00224; PMC: PMC7456929 NTUHi001-A 2020-00-00 2020-00-00 PubMed: 32922264 DOI: 10.3389/fncel.2020.00224Associated cell lines:
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Yamasaki AE, King NE, Matsui H, Jepsen K, Panopoulos AD
Two iPSC lines generated from the bone marrow of a relapsed/refractory AML patient display normal karyotypes and myeloid differentiation potential
Yamasaki AE et al. Two iPSC lines generated from the bone marrow of a relapsed/refractory AML patient display normal karyotypes and myeloid differentiation potential. . 2019-12-00. Pubmed ID: 31739201; DOI: 10.1016/j.scr.2019.101587 NDi002-ANDi002-B 2019-12-00 2019-12-00 PubMed: 31739201 DOI: 10.1016/j.scr.2019.101587 -
Zanon A, Riekschnitz D, von Troyer M, Volpato C, Picard A, Cantaloni C, Di Segni M, Silipigni R, Pramstaller PP, Hicks AA, Pichler I
Generation of an induced pluripotent stem cell line (EURACi005-A) from a Parkinson's disease patient carrying a homozygous exon 3 deletion in the PRKNgene
Zanon A et al. Generation of an induced pluripotent stem cell line (EURACi005-A) from a Parkinson's disease patient carrying a homozygous exon 3 deletion in the PRKNgene. . 2019-12-00. Pubmed ID: 31715428; DOI: 10.1016/j.scr.2019.101624 EURACi005-A 2019-12-00 2019-12-00 PubMed: 31715428 DOI: 10.1016/j.scr.2019.101624Associated cell lines:
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Abdul MM, Ibañez DP, Zhao P, Liu H, Zhong X, Li Y, Zhang M, Li W, Li Y, Ward C, Chen S, Wang D, Qin B, Esteban MA, Wang X, Fan W, Luo Z
Generation of an induced pluripotent stem cell line (GIBHi003-A) from a Parkinson's disease patient with mutant PINK1 (p. I368N)
Abdul MM et al. Generation of an induced pluripotent stem cell line (GIBHi003-A) from a Parkinson's disease patient with mutant PINK1 (p. I368N). . 2019-12-00. Pubmed ID: 31778937; DOI: 10.1016/j.scr.2019.101607 GIBHi003-A 2019-12-00 2019-12-00 PubMed: 31778937 DOI: 10.1016/j.scr.2019.101607Associated cell lines:
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Bouma MJ, Freund C, IJzerman AP, Boomsma DI, Mummery CL, Raymond K
Lymphoblast-derived hiPS cell lines generated from four individuals of a family of genetically unrelated parents and their female monozygotic twins
Bouma MJ et al. Lymphoblast-derived hiPS cell lines generated from four individuals of a family of genetically unrelated parents and their female monozygotic twins. . 2019-12-00. Pubmed ID: 31734644; DOI: 10.1016/j.scr.2019.101654 LUMCi013-ALUMCi014-ALUMCi015-ALUMCi016-A 2019-12-00 2019-12-00 PubMed: 31734644 DOI: 10.1016/j.scr.2019.101654Associated cell lines:
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Martinez-Turrillas R, Rodriguez-Diaz S, Rodriguez-Marquez P, Martin-Mallo A, Salido E, Beck BB, Prosper F, Rodriguez-Madoz JR
Generation of an induced pluripotent stem cell line (CIMAi001-A) from a compound heterozygous Primary Hyperoxaluria Type I (PH1) patient carrying p.G170R and p.R122* mutations in the AGXT gene
Martinez-Turrillas R et al. Generation of an induced pluripotent stem cell line (CIMAi001-A) from a compound heterozygous Primary Hyperoxaluria Type I (PH1) patient carrying p.G170R and p.R122* mutations in the AGXT gene. . 2019-12-00. Pubmed ID: 31715429; DOI: 10.1016/j.scr.2019.101626 CIMAi001-A 2019-12-00 2019-12-00 PubMed: 31715429 DOI: 10.1016/j.scr.2019.101626Associated cell lines:
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Slanzi A, Iannoto G, Rossi B, Zenaro E, Constantin G
In vitro Models of Neurodegenerative Diseases
Slanzi A et al. In vitro Models of Neurodegenerative Diseases. . 2020-00-00. Pubmed ID: 32528949; DOI: 10.3389/fcell.2020.00328; PMC: PMC7247860 CSSi004-ACHOPi002-ACHOPi003-ANUIGi043-ANUIGi043-BNUIGi043-CNUIGi044-ANUIGi044-BNUIGi044-CIGIBi002-AIGIBi003-AIGIBi004-A 2020-00-00 2020-00-00 PubMed: 32528949 DOI: 10.3389/fcell.2020.00328Associated cell lines:
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Xie L, Huang J, Li X, Dai L, Lin X, Zhang J, Luo J, Zhang W
Generation of a homozygous HDAC6 knockout human embryonic stem cell line by CRISPR/Cas9 editing
Xie L et al. Generation of a homozygous HDAC6 knockout human embryonic stem cell line by CRISPR/Cas9 editing. . 2019-12-00. Pubmed ID: 31775087; DOI: 10.1016/j.scr.2019.101610 WAe009-AWAe009-A-21 2019-12-00 2019-12-00 PubMed: 31775087 DOI: 10.1016/j.scr.2019.101610Associated cell lines:
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Benetó N, Cozar M, García-Morant M, Creus-Bachiller E, Vilageliu L, Grinberg D, Canals I
Generation of two compound heterozygous HGSNAT-mutated lines from healthy induced pluripotent stem cells using CRISPR/Cas9 to model Sanfilippo C syndrome
Benetó N et al. Generation of two compound heterozygous HGSNAT-mutated lines from healthy induced pluripotent stem cells using CRISPR/Cas9 to model Sanfilippo C syndrome. . 2019-12-00. Pubmed ID: 31731183; DOI: 10.1016/j.scr.2019.101616 UBi001-AUBi001-A-1UBi001-A-2 2019-12-00 2019-12-00 PubMed: 31731183 DOI: 10.1016/j.scr.2019.101616Associated cell lines:
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Si L, Yang R, Liu J, Dong Y, Zhang H, Xu X
Generation of two ERF gene knockout human embryonic stem cell lines using CRISPR/Cas9 system
Si L et al. Generation of two ERF gene knockout human embryonic stem cell lines using CRISPR/Cas9 system. . 2019-12-00. Pubmed ID: 31743839; DOI: 10.1016/j.scr.2019.101644 WAe001-A-33WAe001-A-34 2019-12-00 2019-12-00 PubMed: 31743839 DOI: 10.1016/j.scr.2019.101644Associated cell lines:
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Trajanoska K, Rivadeneira F
Genomic Medicine: Lessons Learned From Monogenic and Complex Bone Disorders
Trajanoska K et al. Genomic Medicine: Lessons Learned From Monogenic and Complex Bone Disorders. . 2020-00-00. Pubmed ID: 33162933; DOI: 10.3389/fendo.2020.556610; PMC: PMC7581702 MCRIi001-AMCRIi001-A-1 2020-00-00 2020-00-00 PubMed: 33162933 DOI: 10.3389/fendo.2020.556610Associated cell lines:
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Zhang M, Ibañez DP, Fan W, Liu H, Zhong X, Wang X, Li Y, Md Abdul M, Li W, Li Y, Ward C, Chen S, Wang D, Qin B, Esteban MA, Zhao P, Luo Z
Generation of a PARK2 homozygous knockout induced pluripotent stem cell line (GIBHi002-A-1) with two common isoforms abolished
Zhang M et al. Generation of a PARK2 homozygous knockout induced pluripotent stem cell line (GIBHi002-A-1) with two common isoforms abolished. . 2019-12-00. Pubmed ID: 31698191; DOI: 10.1016/j.scr.2019.101602 GIBHi002-AGIBHi002-A-1 2019-12-00 2019-12-00 PubMed: 31698191 DOI: 10.1016/j.scr.2019.101602Associated cell lines:
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Lu C, Sanjana NE
Generation of a knock-in MAP2-tdTomato reporter human embryonic stem cell line with inducible expression of NEUROG2/1 (NYGCe001-A)
Lu C et al. Generation of a knock-in MAP2-tdTomato reporter human embryonic stem cell line with inducible expression of NEUROG2/1 (NYGCe001-A). . 2019-12-00. Pubmed ID: 31707212; DOI: 10.1016/j.scr.2019.101643; PMC: PMC6919562 NYGCe001-A 2019-12-00 2019-12-00 PubMed: 31707212 DOI: 10.1016/j.scr.2019.101643Associated cell lines:
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Kim BY, Ko JM, Park MH, Koo SK
Generation of a patient-specific induced pluripotent stem cell line, KSCBi006-A, for osteogenesis imperfecta type I with the COL1A1, c.3162delT mutation
Kim BY et al. Generation of a patient-specific induced pluripotent stem cell line, KSCBi006-A, for osteogenesis imperfecta type I with the COL1A1, c.3162delT mutation. . 2019-12-00. Pubmed ID: 31715426; DOI: 10.1016/j.scr.2019.101622 KSCBi006-A 2019-12-00 2019-12-00 PubMed: 31715426 DOI: 10.1016/j.scr.2019.101622Associated cell lines:
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Lee Y, Choi HY, Kwon A, Park H, Park MH, Kim JW, Kim MJ, Kim YO, Kwak S, Koo SK
Generation of a PDX1-EGFP reporter human induced pluripotent stem cell line, KSCBi005-A-3, using the CRISPR/Cas9 system
Lee Y et al. Generation of a PDX1-EGFP reporter human induced pluripotent stem cell line, KSCBi005-A-3, using the CRISPR/Cas9 system. . 2019-12-00. Pubmed ID: 31683099; DOI: 10.1016/j.scr.2019.101632 KSCBi005-AKSCBi005-A-3 2019-12-00 2019-12-00 PubMed: 31683099 DOI: 10.1016/j.scr.2019.101632Associated cell lines:
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Srivastava AchalK, Swarup Vishnu, Kumar Vikas, Faruq Mohammed, Singh HimanshuN, Singh Inder
CRISPR/Cas9 technology in neurological disorders: An update for clinicians
Srivastava AchalK et al. CRISPR/Cas9 technology in neurological disorders: An update for clinicians. . 2020-00-00. DOI: 10.4103/aomd.aomd_39_19 WAe009-AWAe009-A-16 2020-00-00 2020-00-00 DOI: 10.4103/aomd.aomd_39_19Associated cell lines:
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Hilderink S, Devalla HD, Bosch L, Wilders R, Verkerk AO
Ultrarapid Delayed Rectifier K(+) Channelopathies in Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes
Hilderink S et al. Ultrarapid Delayed Rectifier K(+) Channelopathies in Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes. . 2020-00-00. Pubmed ID: 32850774; DOI: 10.3389/fcell.2020.00536; PMC: PMC7399090 LUMCi004-A 2020-00-00 2020-00-00 PubMed: 32850774 DOI: 10.3389/fcell.2020.00536Associated cell lines:
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Lamolda M, Montes R, Simón I, Perales S, Martínez-Navajas G, Lopez-Onieva L, Ríos-Pelegrina R, Del Moral RG, Griñan-Lison C, Marchal JA, Lozano ML, Ramos-Mejia V, Rivera J, Bastida JM, Real PJ
GENYOi005-A: An induced pluripotent stem cells (iPSCs) line generated from a patient with Familial Platelet Disorder with associated Myeloid Malignancy (FPDMM) carrying a p.Thr196Ala variant
Lamolda M et al. GENYOi005-A: An induced pluripotent stem cells (iPSCs) line generated from a patient with Familial Platelet Disorder with associated Myeloid Malignancy (FPDMM) carrying a p.Thr196Ala variant. . 2019-12-00. Pubmed ID: 31698193; DOI: 10.1016/j.scr.2019.101603 GENYOi004-AGENYOi005-A 2019-12-00 2019-12-00 PubMed: 31698193 DOI: 10.1016/j.scr.2019.101603Associated cell lines:
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Wen MH, Xie X, Tu J, Lee DF, Chen TY
Generation of a genetically modified human embryonic stem cells expressing fluorescence tagged ATOX1
Wen MH et al. Generation of a genetically modified human embryonic stem cells expressing fluorescence tagged ATOX1. . 2019-12-00. Pubmed ID: 31704540; DOI: 10.1016/j.scr.2019.101631; PMC: PMC6939864 WAe001-AWAe001-A-29 2019-12-00 2019-12-00 PubMed: 31704540 DOI: 10.1016/j.scr.2019.101631Associated cell lines:
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Masneri S, Lanzi G, Ferraro RM, Barisani C, Piovani G, Savio G, Cattalini M, Galli J, Cereda C, Muzi-Falconi M, Orcesi S, Fazzi E, Giliani S
Generation of three isogenic induced Pluripotent Stem Cell lines (iPSCs) from fibroblasts of a patient with Aicardi Goutières Syndrome carrying a c.2471G>A dominant mutation in IFIH1 gene
Masneri S et al. Generation of three isogenic induced Pluripotent Stem Cell lines (iPSCs) from fibroblasts of a patient with Aicardi Goutières Syndrome carrying a c.2471G>A dominant mutation in IFIH1 gene. . 2019-12-00. Pubmed ID: 31698194; DOI: 10.1016/j.scr.2019.101623 UNIBSi009-AUNIBSi009-BUNIBSi009-C 2019-12-00 2019-12-00 PubMed: 31698194 DOI: 10.1016/j.scr.2019.101623Associated cell lines:
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Ferraro RM, Lanzi G, Masneri S, Barisani C, Piovani G, Savio G, Cattalini M, Galli J, Cereda C, Muzi-Falconi M, Orcesi S, Fazzi E, Giliani S
Generation of three iPSC lines from fibroblasts of a patient with Aicardi Goutières Syndrome mutated in TREX1
Ferraro RM et al. Generation of three iPSC lines from fibroblasts of a patient with Aicardi Goutières Syndrome mutated in TREX1. . 2019-12-00. Pubmed ID: 31644995; DOI: 10.1016/j.scr.2019.101580 UNIBSi006-AUNIBSi006-BUNIBSi006-CUNIBSi007-BUNIBSi007-C 2019-12-00 2019-12-00 PubMed: 31644995 DOI: 10.1016/j.scr.2019.101580Associated cell lines:
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Ponsford MJ, Clark J, Mock J, Abinun M, Carne E, El-Shanawany T, Williams PE, Choudhury A, Freeman AF, Gennery AR, Jolles S
Hematopoietic Stem Cell Transplantation and Vasculopathy Associated With STAT3-Dominant-Negative Hyper-IgE Syndrome
Ponsford MJ et al. Hematopoietic Stem Cell Transplantation and Vasculopathy Associated With STAT3-Dominant-Negative Hyper-IgE Syndrome. . 2020-00-00. Pubmed ID: 33014947; DOI: 10.3389/fped.2020.00575; PMC: PMC7511721 NIHTVBi011-ANIHTVBi012-ANIHTVBi013-A 2020-00-00 2020-00-00 PubMed: 33014947 DOI: 10.3389/fped.2020.00575Associated cell lines:
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Angsutararux P, Luanpitpong S, Chingsuwanrote P, Supraditaporn K, Waeteekul S, Terbto P, Lorthongpanich C, Laowtammathron C, U-Pratya Y, Issaragrisil S
Generation of human induced pluripotent stem cell line carrying SCN5AC2204>T Brugada mutation (MUSli009-A-1) introduced by CRISPR/Cas9-mediated genome editing
Angsutararux P et al. Generation of human induced pluripotent stem cell line carrying SCN5AC2204>T Brugada mutation (MUSli009-A-1) introduced by CRISPR/Cas9-mediated genome editing. . 2019-12-00. Pubmed ID: 31677524; DOI: 10.1016/j.scr.2019.101618 MUSIi009-AMUSIi009-A-1 2019-12-00 2019-12-00 PubMed: 31677524 DOI: 10.1016/j.scr.2019.101618Associated cell lines:
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Lito S, Burda P, Baumgartner M, Sloan-Béna F, Táncos Z, Kobolák J, Dinnyés A, Krause KH, Marteyn A
Generation of human induced pluripotent stem cell line UNIGEi001-A from a 2-years old patient with Mucopolysaccharidosis type IH disease
Lito S et al. Generation of human induced pluripotent stem cell line UNIGEi001-A from a 2-years old patient with Mucopolysaccharidosis type IH disease. . 2019-12-00. Pubmed ID: 31678774; DOI: 10.1016/j.scr.2019.101604 UNIGEi001-A 2019-12-00 2019-12-00 PubMed: 31678774 DOI: 10.1016/j.scr.2019.101604Associated cell lines:
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Drummond NJ, Singh Dolt K, Canham MA, Kilbride P, Morris GJ, Kunath T
Cryopreservation of Human Midbrain Dopaminergic Neural Progenitor Cells Poised for Neuronal Differentiation
Drummond NJ et al. Cryopreservation of Human Midbrain Dopaminergic Neural Progenitor Cells Poised for Neuronal Differentiation. . 2020-00-00. Pubmed ID: 33224948; DOI: 10.3389/fcell.2020.578907; PMC: PMC7674628 RCe021-A 2020-00-00 2020-00-00 PubMed: 33224948 DOI: 10.3389/fcell.2020.578907Associated cell lines:
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Lorthongpanich C, Jiamvoraphong N, Supakun P, Damkham N, Terbto P, Waeteekul S, U-Pratya Y, Laowtammathron C, Issaragrisil S
Generation of a WWTR1 mutation induced pluripotent stem cell line, MUSIi012-A-1, using CRISPR/Cas9
Lorthongpanich C et al. Generation of a WWTR1 mutation induced pluripotent stem cell line, MUSIi012-A-1, using CRISPR/Cas9. . 2019-12-00. Pubmed ID: 31677525; DOI: 10.1016/j.scr.2019.101634 MUSIi012-AMUSIi012-A-1 2019-12-00 2019-12-00 PubMed: 31677525 DOI: 10.1016/j.scr.2019.101634Associated cell lines:
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Chulpanova Daria S., Shaimardanova Alisa A., Solovyeva Valeriya V., Mullagulova Aysilu I., Kitaeva Kristina V., Allegrucci Cinzia, Rizvanov Albert A.
iPSCs for modeling lysosomal storage diseases
Chulpanova Daria S. et al. iPSCs for modeling lysosomal storage diseases. . 2020-00-00. DOI: 10.1016/b978-0-12-822227-0.00001-6 UKWNLi001-AAKOSi001-ATRNDi004-ITRNDi007-BTRNDi009-CINSAi001-A 2020-00-00 2020-00-00 DOI: 10.1016/b978-0-12-822227-0.00001-6Associated cell lines:
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Jin H, Yu Z, Navarengom K, Liu Y, Dmitrieva N, Hsu AP, Schwartzbeck R, Cudrici C, Ferrante EA, Yang D, Holland SM, Freeman AF, Boehm M, Chen G
Generation of human induced pluripotent stem cell lines (NIHTVBi011-A, NIHTVBi012-A, NIHTVBi013-A) from autosomal dominant Hyper IgE syndrome (AD-HIES) patients carrying STAT3 mutation
Jin H et al. Generation of human induced pluripotent stem cell lines (NIHTVBi011-A, NIHTVBi012-A, NIHTVBi013-A) from autosomal dominant Hyper IgE syndrome (AD-HIES) patients carrying STAT3 mutation. . 2019-12-00. Pubmed ID: 31707214; DOI: 10.1016/j.scr.2019.101586; PMC: PMC6957122 NIHTVBi011-ANIHTVBi012-ANIHTVBi013-A 2019-12-00 2019-12-00 PubMed: 31707214 DOI: 10.1016/j.scr.2019.101586Associated cell lines:
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Handal Tayma, Eiges Rachel
The contribution of human pluripotent stem cells to the study of myotonic dystrophy type 1
Handal Tayma et al. The contribution of human pluripotent stem cells to the study of myotonic dystrophy type 1. . 2020-00-00. DOI: 10.1016/b978-0-12-822227-0.00008-9 CHUQi001-A 2020-00-00 2020-00-00 DOI: 10.1016/b978-0-12-822227-0.00008-9Associated cell lines:
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Zhang Q, Li Z, Sun H, Zhang S, Zhang J, Wang Y, Fang H, Xu Y
Corrigendum to 'Generation of induced pluripotent stem cell line (ZZUi0012-a) from a patient with Fahr's disease caused by a novel mutation in SLC20A2 gene' [stem cell research volume 35, March 2019, 101,395]
Zhang Q et al. Corrigendum to 'Generation of induced pluripotent stem cell line (ZZUi0012-a) from a patient with Fahr's disease caused by a novel mutation in SLC20A2 gene' [stem cell research volume 35, March 2019, 101,395]. . 2019-12-00. Pubmed ID: 31439445; DOI: 10.1016/j.scr.2019.101507 ZZUi012-A 2019-12-00 2019-12-00 PubMed: 31439445 DOI: 10.1016/j.scr.2019.101507Associated cell lines:
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Varma R, Soleas JP, Waddell TK, Karoubi G, McGuigan AP
Current strategies and opportunities to manufacture cells for modeling human lungs
Varma R et al. Current strategies and opportunities to manufacture cells for modeling human lungs. . 2020-00-00. Pubmed ID: 32835746; DOI: 10.1016/j.addr.2020.08.005; PMC: PMC7442933 MHHi006-AMHHi006-A-4 2020-00-00 2020-00-00 PubMed: 32835746 DOI: 10.1016/j.addr.2020.08.005Associated cell lines:
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Tofoli FA, Chien HF, Barbosa ER, Pereira LV
Generation of 5 hiPSC lines derived from three unrelated idiopathic Parkinson disease patients and two unrelated healthy control individuals
Tofoli FA et al. Generation of 5 hiPSC lines derived from three unrelated idiopathic Parkinson disease patients and two unrelated healthy control individuals. . 2019-12-00. Pubmed ID: 31710912; DOI: 10.1016/j.scr.2019.101640 LANCEi014-ALANCEi015-ALANCEi016-ALANCEi017-ALANCEi018-A 2019-12-00 2019-12-00 PubMed: 31710912 DOI: 10.1016/j.scr.2019.101640Associated cell lines:
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Wohlschlegel J, Letellier C, Liu B, Méjécase C, Slembrouck-Brec A, Condroyer C, Michiels C, Sahel JA, Reichman S, Zeitz C, Goureau O, Audo I
Generation of human induced pluripotent stem cell lines from a patient with ITM2B-related retinal dystrophy and a non mutated brother
Wohlschlegel J et al. Generation of human induced pluripotent stem cell lines from a patient with ITM2B-related retinal dystrophy and a non mutated brother. . 2019-12-00. Pubmed ID: 31731182; DOI: 10.1016/j.scr.2019.101625 IDVi003-AIDVi004-AIDVi003-BIDVi003-CIDVi004-B 2019-12-00 2019-12-00 PubMed: 31731182 DOI: 10.1016/j.scr.2019.101625 -
Völkner C, Peter F, Liedtke M, Krohn S, Lindner I, Murua Escobar H, Cimmaruta C, Lukas J, Hermann A, Frech MJ
Generation of the Niemann-Pick type C2 patient-derived iPSC line AKOSi001-A
Völkner C et al. Generation of the Niemann-Pick type C2 patient-derived iPSC line AKOSi001-A. . 2019-12-00. Pubmed ID: 31669975; DOI: 10.1016/j.scr.2019.101606 AKOSi001-A 2019-12-00 2019-12-00 PubMed: 31669975 DOI: 10.1016/j.scr.2019.101606Associated cell lines:
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Jing Y, Zhou Y, Wang C, Liu J, Guo Y, Mao S, Chan HF, Tang S, Chen J
Establishment of a non-integrate iPS cell line CSUASOi002-A, from urine-derived cells of a female patient with macular corneal dystrophy carrying compound heterozygous CHST6 mutations
Jing Y et al. Establishment of a non-integrate iPS cell line CSUASOi002-A, from urine-derived cells of a female patient with macular corneal dystrophy carrying compound heterozygous CHST6 mutations. . 2019-12-00. Pubmed ID: 31669782; DOI: 10.1016/j.scr.2019.101598 CSUASOi002-A 2019-12-00 2019-12-00 PubMed: 31669782 DOI: 10.1016/j.scr.2019.101598Associated cell lines:
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Plant AL, Halter M, Stinson J
Probing pluripotency gene regulatory networks with quantitative live cell imaging
Plant AL et al. Probing pluripotency gene regulatory networks with quantitative live cell imaging. . 2020-00-00. Pubmed ID: 33101611; DOI: 10.1016/j.csbj.2020.09.025; PMC: PMC7560648 MCRIi001-AMCRIi001-A-2 2020-00-00 2020-00-00 PubMed: 33101611 DOI: 10.1016/j.csbj.2020.09.025Associated cell lines:
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Miller DB, Piccolo SR
CompoundHetVIP: Compound Heterozygous Variant Identification Pipeline
Miller DB et al. CompoundHetVIP: Compound Heterozygous Variant Identification Pipeline. . 2020-00-00. Pubmed ID: 33680433; DOI: 10.12688/f1000research.26848.2; PMC: PMC7905494 TRNDi002-B 2020-00-00 2020-00-00 PubMed: 33680433 DOI: 10.12688/f1000research.26848.2Associated cell lines:
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Goversen B, Jonsson MK, van den Heuvel NH, Rijken R, Vos MA, van Veen TA, de Boer TP
The influence of hERG1a and hERG1b isoforms on drug safety screening in iPSC-CMs
Goversen B et al. The influence of hERG1a and hERG1b isoforms on drug safety screening in iPSC-CMs. . 2019-12-00. Pubmed ID: 30826123; DOI: 10.1016/j.pbiomolbio.2019.02.003 PSMi003-A 2019-12-00 2019-12-00 PubMed: 30826123 DOI: 10.1016/j.pbiomolbio.2019.02.003Associated cell lines:
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Lu L, Jin W, Wang LL
RECQ DNA Helicases and Osteosarcoma
Lu L et al. RECQ DNA Helicases and Osteosarcoma. . 2020-00-00. Pubmed ID: 32767233; DOI: 10.1007/978-3-030-43085-6_3 REGUi003-A 2020-00-00 2020-00-00 PubMed: 32767233 DOI: 10.1007/978-3-030-43085-6_3Associated cell lines:
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Belleghem Sarah Miho Van, Mahadik Bhushan, Snodderly Kirstie Lane, Fisher John P.
Overview of Tissue Engineering Concepts and Applications
Belleghem Sarah Miho Van et al. Overview of Tissue Engineering Concepts and Applications. . 2020-00-00. DOI: 10.1016/b978-0-12-816137-1.00081-7 MUSIi006-A 2020-00-00 2020-00-00 DOI: 10.1016/b978-0-12-816137-1.00081-7Associated cell lines:
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Ferraro RM, Masneri S, Lanzi G, Barisani C, Piovani G, Savio G, Cattalini M, Galli J, Cereda C, Muzi-Falconi M, Orcesi S, Fazzi E, Giliani S
Establishment of three iPSC lines from fibroblasts of a patient with Aicardi Goutières syndrome mutated in RNaseH2B
Ferraro RM et al. Establishment of three iPSC lines from fibroblasts of a patient with Aicardi Goutières syndrome mutated in RNaseH2B. . 2019-12-00. Pubmed ID: 31678772; DOI: 10.1016/j.scr.2019.101620 UNIBSi007-AUNIBSi007-BUNIBSi007-C 2019-12-00 2019-12-00 PubMed: 31678772 DOI: 10.1016/j.scr.2019.101620Associated cell lines:
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Fang F, Li Z, Zhao Q, Ye Z, Gu X, Pan F, Li H, Xiang W, Xiong C
Induced Pluripotent Stem Cells Derived From Two Idiopathic Azoospermia Patients Display Compromised Differentiation Potential for Primordial Germ Cell Fate
Fang F et al. Induced Pluripotent Stem Cells Derived From Two Idiopathic Azoospermia Patients Display Compromised Differentiation Potential for Primordial Germ Cell Fate. . 2020-00-00. Pubmed ID: 32671061; DOI: 10.3389/fcell.2020.00432; PMC: PMC7331483 HUSTi001-A 2020-00-00 2020-00-00 PubMed: 32671061 DOI: 10.3389/fcell.2020.00432Associated cell lines:
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Jelinkova S, Vilotic A, Pribyl J, Aimond F, Salykin A, Acimovic I, Pesl M, Caluori G, Klimovic S, Urban T, Dobrovolna H, Soska V, Skladal P, Lacampagne A, Dvorak P, Meli AC, Rotrekl V
DMD Pluripotent Stem Cell Derived Cardiac Cells Recapitulate in vitro Human Cardiac Pathophysiology
Jelinkova S et al. DMD Pluripotent Stem Cell Derived Cardiac Cells Recapitulate in vitro Human Cardiac Pathophysiology. . 2020-00-00. Pubmed ID: 32656189; DOI: 10.3389/fbioe.2020.00535; PMC: PMC7325914 MUNIe005-AMUNIe007-AMUNIi001-AMUNIi003-A 2020-00-00 2020-00-00 PubMed: 32656189 DOI: 10.3389/fbioe.2020.00535Associated cell lines:
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Sharipova DV, Kovalenko VR, Bairamova EM, Vartanova VA, Grigor'eva EV, Vyatkin YV, Khabarova EA, Rzaev DA, Zakian SM, Medvedev SP
Generation of two iPSC lines, (ICGi015-A and ICGi015-B), by reprogramming peripheral blood mononuclear cells from a patient with Parkinson's disease
Sharipova DV et al. Generation of two iPSC lines, (ICGi015-A and ICGi015-B), by reprogramming peripheral blood mononuclear cells from a patient with Parkinson's disease. . 2019-12-00. Pubmed ID: 31733442; DOI: 10.1016/j.scr.2019.101652 ICGi008-AICGi008-BICGi015-AICGi015-B 2019-12-00 2019-12-00 PubMed: 31733442 DOI: 10.1016/j.scr.2019.101652 -
Chen L, Wang Y, Xie J
A Human iPSC Line Carrying a de novo Pathogenic FUS Mutation Identified in a Patient With Juvenile ALS Differentiated Into Motor Neurons With Pathological Characteristics
Chen L et al. A Human iPSC Line Carrying a de novo Pathogenic FUS Mutation Identified in a Patient With Juvenile ALS Differentiated Into Motor Neurons With Pathological Characteristics. . 2020-00-00. Pubmed ID: 33093822; DOI: 10.3389/fncel.2020.00273; PMC: PMC7507938 ZZUNEUi010-A 2020-00-00 2020-00-00 PubMed: 33093822 DOI: 10.3389/fncel.2020.00273Associated cell lines:
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Wu SS, Li QC, Yin CQ, Xue W, Song CQ
Advances in CRISPR/Cas-based Gene Therapy in Human Genetic Diseases
Wu SS et al. Advances in CRISPR/Cas-based Gene Therapy in Human Genetic Diseases. . 2020-00-00. Pubmed ID: 32292501; DOI: 10.7150/thno.43360; PMC: PMC7150498 MCRIi001-AMCRIi001-A-1 2020-00-00 2020-00-00 PubMed: 32292501 DOI: 10.7150/thno.43360Associated cell lines:
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Smirnikhina SA, Kondrateva EV, Adilgereeva EP, Anuchina AA, Zaynitdinova MI, Slesarenko YS, Ershova AS, Ustinov KD, Yasinovsky MI, Amelina EL, Voronina ES, Yakushina VD, Tabakov VY, Lavrov AV
P.F508del editing in cells from cystic fibrosis patients
Smirnikhina SA et al. P.F508del editing in cells from cystic fibrosis patients. . 2020-00-00. Pubmed ID: 33175893; DOI: 10.1371/journal.pone.0242094; PMC: PMC7657551 RCMGi001-A 2020-00-00 2020-00-00 PubMed: 33175893 DOI: 10.1371/journal.pone.0242094Associated cell lines:
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Park H, Han J, Lee Y, Kwak S, Koo SK
Generation of human induced pluripotent stem cells from peripheral blood mononuclear cells of a Senior-Loken syndrome patient
Park H et al. Generation of human induced pluripotent stem cells from peripheral blood mononuclear cells of a Senior-Loken syndrome patient. . 2019-12-00. Pubmed ID: 31734643; DOI: 10.1016/j.scr.2019.101648 KSCBi010-A 2019-12-00 2019-12-00 PubMed: 31734643 DOI: 10.1016/j.scr.2019.101648Associated cell lines:
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Bakhti M, Scheibner K, Tritschler S, Bastidas-Ponce A, Tarquis-Medina M, Theis FJ, Lickert H
Establishment of a high-resolution 3D modeling system for studying pancreatic epithelial cell biology in vitro
Bakhti M et al. Establishment of a high-resolution 3D modeling system for studying pancreatic epithelial cell biology in vitro. . 2019-12-00. Pubmed ID: 31767167; DOI: 10.1016/j.molmet.2019.09.005; PMC: PMC6812400 HMGUi001-A 2019-12-00 2019-12-00 PubMed: 31767167 DOI: 10.1016/j.molmet.2019.09.005Associated cell lines:
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Duarte AJ, Ribeiro D, Santos R, Moreira L, Bragança J, Amaral O
Induced pluripotent stem cell line (INSAi001-A) from a Gaucher disease type 3 patient compound heterozygote for mutations in the GBA1 gene
Duarte AJ et al. Induced pluripotent stem cell line (INSAi001-A) from a Gaucher disease type 3 patient compound heterozygote for mutations in the GBA1 gene. . 2019-12-00. Pubmed ID: 31678773; DOI: 10.1016/j.scr.2019.101595 INSAi001-A 2019-12-00 2019-12-00 PubMed: 31678773 DOI: 10.1016/j.scr.2019.101595Associated cell lines:
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Reich M, Paris I, Ebeling M, Dahm N, Schweitzer C, Reinhardt D, Schmucki R, Prasad M, Köchl F, Leist M, Cowley SA, Zhang JD, Patsch C, Gutbier S, Britschgi M
Alzheimer's Risk Gene TREM2 Determines Functional Properties of New Type of Human iPSC-Derived Microglia
Reich M et al. Alzheimer's Risk Gene TREM2 Determines Functional Properties of New Type of Human iPSC-Derived Microglia. . 2020-00-00. Pubmed ID: 33613545; DOI: 10.3389/fimmu.2020.617860; PMC: PMC7887311 BIONi010-C 2020-00-00 2020-00-00 PubMed: 33613545 DOI: 10.3389/fimmu.2020.617860Associated cell lines:
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Überbacher C, Obergasteiger J, Volta M, Venezia S, Müller S, Pesce I, Pizzi S, Lamonaca G, Picard A, Cattelan G, Malpeli G, Zoli M, Beccano-Kelly D, Flynn R, Wade-Martins R, Pramstaller PP, Hicks AA, Cowley SA, Corti C
Application of CRISPR/Cas9 editing and digital droplet PCR in human iPSCs to generate novel knock-in reporter lines to visualize dopaminergic neurons
Überbacher C et al. Application of CRISPR/Cas9 editing and digital droplet PCR in human iPSCs to generate novel knock-in reporter lines to visualize dopaminergic neurons. . 2019-12-00. Pubmed ID: 31733438; DOI: 10.1016/j.scr.2019.101656; PMC: PMC7322529 STBCi026-CSTBCi063-A 2019-12-00 2019-12-00 PubMed: 31733438 DOI: 10.1016/j.scr.2019.101656Associated cell lines:
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Yang X, Liu Y, Zhou T, Zhang H, Dong R, Li Y, Liu N, Liu Y, Gai Z
An induced pluripotent stem cells line (SDQLCHi014-A) derived from urine cells of a patient with ASD and hyperactivity carrying a 303 kb de novo deletion at chr3p26.1 implicating GRM7 gene
Yang X et al. An induced pluripotent stem cells line (SDQLCHi014-A) derived from urine cells of a patient with ASD and hyperactivity carrying a 303 kb de novo deletion at chr3p26.1 implicating GRM7 gene. . 2019-12-00. Pubmed ID: 31707215; DOI: 10.1016/j.scr.2019.101635 SDQLCHi014-A 2019-12-00 2019-12-00 PubMed: 31707215 DOI: 10.1016/j.scr.2019.101635Associated cell lines:
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Zhou H, Gong Y, Wu Q, Ye X, Yu B, Lu C, Jiang W, Ye J, Fu Z
Rare Diseases Related with Lipoprotein Metabolism
Zhou H et al. Rare Diseases Related with Lipoprotein Metabolism. . 2020-00-00. Pubmed ID: 32705600; DOI: 10.1007/978-981-15-6082-8_11 TRNDi009-C 2020-00-00 2020-00-00 PubMed: 32705600 DOI: 10.1007/978-981-15-6082-8_11Associated cell lines:
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Masneri S, Ferraro RM, Lanzi G, Piovani G, Mori L, Barisani C, Moratto D, Plebani A, Badolato R, Soresina A, Giliani S
Generation of induced Pluripotent Stem Cells (UNIBSi008-A, UNIBSi008-B, UNIBSi008-C) from an Ataxia-Telangiectasia (AT) patient carrying a novel homozygous deletion in ATM gene
Masneri S et al. Generation of induced Pluripotent Stem Cells (UNIBSi008-A, UNIBSi008-B, UNIBSi008-C) from an Ataxia-Telangiectasia (AT) patient carrying a novel homozygous deletion in ATM gene. . 2019-12-00. Pubmed ID: 31669783; DOI: 10.1016/j.scr.2019.101596 UNIBSi008-AUNIBSi008-BUNIBSi008-C 2019-12-00 2019-12-00 PubMed: 31669783 DOI: 10.1016/j.scr.2019.101596Associated cell lines:
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Guan J, Liu X, Zhang H, Lv Y, Wang X, Yang X, Ma Y, Liu Q, Liu Y, Sun W
Generation of an iPSC line (SDQLCHi015-A) from peripheral blood mononuclear cells of a patient with mental retardation type 15 carrying c.1007_1011del, p.(Ile336fs) in CUL4B gene
Guan J et al. Generation of an iPSC line (SDQLCHi015-A) from peripheral blood mononuclear cells of a patient with mental retardation type 15 carrying c.1007_1011del, p.(Ile336fs) in CUL4B gene. . 2019-12-00. Pubmed ID: 31678776; DOI: 10.1016/j.scr.2019.101628 SDQLCHi015-A 2019-12-00 2019-12-00 PubMed: 31678776 DOI: 10.1016/j.scr.2019.101628Associated cell lines:
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Shindo A, Ishikawa H, Ii Y, Niwa A, Tomimoto H
Clinical Features and Experimental Models of Cerebral Small Vessel Disease
Shindo A et al. Clinical Features and Experimental Models of Cerebral Small Vessel Disease. . 2020-00-00. Pubmed ID: 32431603; DOI: 10.3389/fnagi.2020.00109; PMC: PMC7214616 LUMCi005-A 2020-00-00 2020-00-00 PubMed: 32431603 DOI: 10.3389/fnagi.2020.00109Associated cell lines:
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Dorszewska J, Kowalska M, Grzegorski T, Dziewulska D, Karmelita-Katulska K, Barciszewska AM, Prendecki M, Gorczyński W, Kozubski W
Clinical presentation of Y189C mutation of the NOTCH3 gene in the Polish family with CADASIL
Dorszewska J et al. Clinical presentation of Y189C mutation of the NOTCH3 gene in the Polish family with CADASIL. . 2020-00-00. Pubmed ID: 32337960; DOI: 10.5114/fn.2020.94009 IDISi001-A 2020-00-00 2020-00-00 PubMed: 32337960 DOI: 10.5114/fn.2020.94009Associated cell lines:
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Ma Y, Zhang H, Zhang S, Dong R, Yang X, Li Y, Guan J, Gai Z, Liu Y
An integration-free iPSC line (SDQLCHi012-A) derived from a patient with inflammatory bowel disease- 28 carrying compound heterozygote mutations in IL10RA gene
Ma Y et al. An integration-free iPSC line (SDQLCHi012-A) derived from a patient with inflammatory bowel disease- 28 carrying compound heterozygote mutations in IL10RA gene. . 2019-12-00. Pubmed ID: 31648101; DOI: 10.1016/j.scr.2019.101577 SDQLCHi012-A 2019-12-00 2019-12-00 PubMed: 31648101 DOI: 10.1016/j.scr.2019.101577Associated cell lines:
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Zhang H, Ma Y, Li X, Yang X, Li Y, Guan J, Dong R, Gai Z, Liu Y
An integration-free iPSC line (SDQLCHi013-A) derived from a patient with maple syrup urine disease carrying compound heterozygote mutations in BCKDHA gene
Zhang H et al. An integration-free iPSC line (SDQLCHi013-A) derived from a patient with maple syrup urine disease carrying compound heterozygote mutations in BCKDHA gene. . 2019-12-00. Pubmed ID: 31775088; DOI: 10.1016/j.scr.2019.101585 SDQLCHi013-A 2019-12-00 2019-12-00 PubMed: 31775088 DOI: 10.1016/j.scr.2019.101585Associated cell lines:
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Newman Katie, Argyriou Amerikos, Wang Tao
Induced pluripotent stem cell modeling of genetic small vessel disease
Newman Katie et al. Induced pluripotent stem cell modeling of genetic small vessel disease. . 2020-00-00. DOI: 10.1016/b978-0-12-822227-0.00007-7 IDISi001-A 2020-00-00 2020-00-00 DOI: 10.1016/b978-0-12-822227-0.00007-7Associated cell lines:
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Gao X, Gao X, Zhao H, Cui W, Tan M, Deng H
Establishment of induced pluripotent stem cell line (GSPHi001-A) from a 6-year old female with nephrotic syndrome
Gao X et al. Establishment of induced pluripotent stem cell line (GSPHi001-A) from a 6-year old female with nephrotic syndrome. . 2019-12-00. Pubmed ID: 31759290; DOI: 10.1016/j.scr.2019.101661 GSPHi001-A 2019-12-00 2019-12-00 PubMed: 31759290 DOI: 10.1016/j.scr.2019.101661Associated cell lines:
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Shnaider TA, Pristyazhnyuk IE, Menzorov AG, Matveeva NM, Nikitina TV, Khabarova AA, Skryabin NA, Kashevarova AA, Lopatkina ME, Nazarenko LP, Lebedev IN, Serov OL
Generation of four iPSC lines from two siblings with a microdeletion at the CNTN6 gene and intellectual disability
Shnaider TA et al. Generation of four iPSC lines from two siblings with a microdeletion at the CNTN6 gene and intellectual disability. . 2019-12-00. Pubmed ID: 31678775; DOI: 10.1016/j.scr.2019.101591 ICGi009-AICGi013-AICGi013-BICGi009-B 2019-12-00 2019-12-00 PubMed: 31678775 DOI: 10.1016/j.scr.2019.101591 -
Ramme AP, Faust D, Koenig L, Marx U
Generation of four integration-free iPSC lines from related human donors
Ramme AP et al. Generation of four integration-free iPSC lines from related human donors. . 2019-12-00. Pubmed ID: 31704539; DOI: 10.1016/j.scr.2019.101615 TISSUi001-ATISSUi002-ATISSUi003-ATISSUi005-A 2019-12-00 2019-12-00 PubMed: 31704539 DOI: 10.1016/j.scr.2019.101615Associated cell lines:
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Wang Y, Sun H, Wang Z, Yue Y, Zhang R, Yang J, Liu Y, Liu H, Zhang Q, Zhang S, Zhang J, Xu Y, Shi C
Generation of induced pluripotent stem cell line (ZZUi0014-A) from a patient with spinocerebellar ataxia type 3
Wang Y et al. Generation of induced pluripotent stem cell line (ZZUi0014-A) from a patient with spinocerebellar ataxia type 3. . 2019-12-00. Pubmed ID: 31639609; DOI: 10.1016/j.scr.2019.101564 ZZUi014-A 2019-12-00 2019-12-00 PubMed: 31639609 DOI: 10.1016/j.scr.2019.101564Associated cell lines:
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Díaz-Guerra E, Rodríguez-Traver E, Moreno-Jiménez EP, de Rojas I, Rodríguez C, Orera M, Hernández I, Ruiz A, Vicario C
An integration-free iPSC line, ICCSICi007-A, derived from a female Alzheimer's disease patient with the APOE-ε4/ε4 alleles
Díaz-Guerra E et al. An integration-free iPSC line, ICCSICi007-A, derived from a female Alzheimer's disease patient with the APOE-ε4/ε4 alleles. . 2019-12-00. Pubmed ID: 31698192; DOI: 10.1016/j.scr.2019.101588 ICCSICi007-A 2019-12-00 2019-12-00 PubMed: 31698192 DOI: 10.1016/j.scr.2019.101588Associated cell lines:
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Kolagar TA, Farzaneh M, Nikkar N, Khoshnam SE
Human Pluripotent Stem Cells in Neurodegenerative Diseases: Potentials, Advances and Limitations
Kolagar TA et al. Human Pluripotent Stem Cells in Neurodegenerative Diseases: Potentials, Advances and Limitations. . 2020-00-00. Pubmed ID: 31441732; DOI: 10.2174/1574888x14666190823142911 CSSi004-A 2020-00-00 2020-00-00 PubMed: 31441732 DOI: 10.2174/1574888x14666190823142911Associated cell lines:
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Fuchs NV, Schieck M, Neuenkirch M, Tondera C, Schmitz H, des Portes V, Germanaud D, Steinemann D, Göhring G, König R
Induced pluripotent stem cells (iPSCs) derived from a renpenning syndrome patient with c.459_462delAGAG mutation in PQBP1 (PEIi001-A)
Fuchs NV et al. Induced pluripotent stem cells (iPSCs) derived from a renpenning syndrome patient with c.459_462delAGAG mutation in PQBP1 (PEIi001-A). . 2019-12-00. Pubmed ID: 31698189; DOI: 10.1016/j.scr.2019.101592 PEIi001-A 2019-12-00 2019-12-00 PubMed: 31698189 DOI: 10.1016/j.scr.2019.101592Associated cell lines:
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Zhang Y, Li A, Wang J, Wang G, Wang D
Generation of induced pluripotent stem cells (iPSCs) from an infant with Pompe disease carrying with compound mutations of R608X and E888X in GAA gene
Zhang Y et al. Generation of induced pluripotent stem cells (iPSCs) from an infant with Pompe disease carrying with compound mutations of R608X and E888X in GAA gene. . 2019-12-00. Pubmed ID: 31743840; DOI: 10.1016/j.scr.2019.101621 XACHi002-A 2019-12-00 2019-12-00 PubMed: 31743840 DOI: 10.1016/j.scr.2019.101621Associated cell lines:
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Schuster J, Laan L, Klar J, Jin Z, Huss M, Korol S, Noraddin FH, Sobol M, Birnir B, Dahl N
Transcriptomes of Dravet syndrome iPSC derived GABAergic cells reveal dysregulated pathways for chromatin remodeling and neurodevelopment
Schuster J et al. Transcriptomes of Dravet syndrome iPSC derived GABAergic cells reveal dysregulated pathways for chromatin remodeling and neurodevelopment. . 2019-12-00. Pubmed ID: 31445158; DOI: 10.1016/j.nbd.2019.104583 UUIGPi006-AUUIGPi007-AUUIGPi008-A 2019-12-00 2019-12-00 PubMed: 31445158 DOI: 10.1016/j.nbd.2019.104583Associated cell lines:
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Eintracht J, Toms M, Moosajee M
The Use of Induced Pluripotent Stem Cells as a Model for Developmental Eye Disorders
Eintracht J et al. The Use of Induced Pluripotent Stem Cells as a Model for Developmental Eye Disorders. . 2020-00-00. Pubmed ID: 32973457; DOI: 10.3389/fncel.2020.00265; PMC: PMC7468397 MCRIi001-AMCRIi001-A-1 2020-00-00 2020-00-00 PubMed: 32973457 DOI: 10.3389/fncel.2020.00265Associated cell lines:
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Sanchez-Duffhues G, Mikkers H, de Jong D, Szuhai K, de Vries TJ, Freund C, Bravenboer N, van Es RJJ, Netelenbos JC, Goumans MJ, Eekhoff EMW, Ten Dijke P
Generation of Fibrodysplasia ossificans progressiva and control integration free iPSC lines from periodontal ligament fibroblasts
Sanchez-Duffhues G et al. Generation of Fibrodysplasia ossificans progressiva and control integration free iPSC lines from periodontal ligament fibroblasts. . 2019-12-00. Pubmed ID: 31733439; DOI: 10.1016/j.scr.2019.101639 LUMCi009-ALUMCi010-A 2019-12-00 2019-12-00 PubMed: 31733439 DOI: 10.1016/j.scr.2019.101639Associated cell lines:
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Beffagna G, Sommariva E, Bellin M
Mechanotransduction and Adrenergic Stimulation in Arrhythmogenic Cardiomyopathy: An Overview of in vitro and in vivo Models
Beffagna G et al. Mechanotransduction and Adrenergic Stimulation in Arrhythmogenic Cardiomyopathy: An Overview of in vitro and in vivo Models. . 2020-00-00. Pubmed ID: 33281612; DOI: 10.3389/fphys.2020.568535; PMC: PMC7689294 LUMCi027-ALUMCi027-A-1 2020-00-00 2020-00-00 PubMed: 33281612 DOI: 10.3389/fphys.2020.568535Associated cell lines:
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Shrestha R, Wen YT, Tsai RK
Generation of hiPSC line TCIERi001-A from normal human epidermal keratinocytes
Shrestha R et al. Generation of hiPSC line TCIERi001-A from normal human epidermal keratinocytes. . 2019-12-00. Pubmed ID: 31683100; DOI: 10.1016/j.scr.2019.101590 TCIERi001-A 2019-12-00 2019-12-00 PubMed: 31683100 DOI: 10.1016/j.scr.2019.101590Associated cell lines:
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Arias-Fuenzalida J, Yu J, Du L, Custodio J, Notarangelo LD, Hammarström L, Pan-Hammarström Q
Generation of human induced pluripotent stem cell lines from patients with selective IgA deficiency
Arias-Fuenzalida J et al. Generation of human induced pluripotent stem cell lines from patients with selective IgA deficiency. . 2019-12-00. Pubmed ID: 31689593; DOI: 10.1016/j.scr.2019.101613 PHAi001-APHAi002-APHAi001-BPHAi002-B 2019-12-00 2019-12-00 PubMed: 31689593 DOI: 10.1016/j.scr.2019.101613 -
Zhang H, Ma Y, Yu S, Yang X, Li Y, Guan J, Dong R, Gai Z, Liu Y
Establishment of a human iPSC line (SDQLCHi010-A) from a patient with optic nerve malformation carrying a heterozygous mutation in PAX6 gene
Zhang H et al. Establishment of a human iPSC line (SDQLCHi010-A) from a patient with optic nerve malformation carrying a heterozygous mutation in PAX6 gene. . 2019-12-00. Pubmed ID: 31707209; DOI: 10.1016/j.scr.2019.101611 SDQLCHi003-ASDQLCHi010-A 2019-12-00 2019-12-00 PubMed: 31707209 DOI: 10.1016/j.scr.2019.101611Associated cell lines:
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Kim BY, Lee JS, Kim YO, Park MH, Koo SK
Generation of patient-specific induced pluripotent stem cells (KSCBi007-A) derived from a patient with Prader-Willi syndrome retain maternal uniparental disomy (UPD)
Kim BY et al. Generation of patient-specific induced pluripotent stem cells (KSCBi007-A) derived from a patient with Prader-Willi syndrome retain maternal uniparental disomy (UPD). . 2019-12-00. Pubmed ID: 31756696; DOI: 10.1016/j.scr.2019.101647 KSCBi007-A 2019-12-00 2019-12-00 PubMed: 31756696 DOI: 10.1016/j.scr.2019.101647Associated cell lines:
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Cavalcante BRR, Aragão-França LS, Sampaio GLA, Nonaka CKV, Oliveira MS, Campos GS, Sardi SI, Dias BRS, Menezes JPB, Rocha VPC, Rossi EA, Paredes BD, Martins GLS, Allahdadi KJ, Peixoto LR, Barbosa-Filho JM, Souza BSF, Soares MBP
Betulinic Acid Exerts Cytoprotective Activity on Zika Virus-Infected Neural Progenitor Cells
Cavalcante BRR et al. Betulinic Acid Exerts Cytoprotective Activity on Zika Virus-Infected Neural Progenitor Cells. . 2020-00-00. Pubmed ID: 33251156; DOI: 10.3389/fcimb.2020.558324; PMC: PMC7674920 CBTCi001-A 2020-00-00 2020-00-00 PubMed: 33251156 DOI: 10.3389/fcimb.2020.558324Associated cell lines:
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Liu Z, Yao M, Yao H, Hu G, Qin B
Generation of Rybp homozygous knockout murine ES cell line GIBHe001-A-1 by using CRISPR/Cas9 technology
Liu Z et al. Generation of Rybp homozygous knockout murine ES cell line GIBHe001-A-1 by using CRISPR/Cas9 technology. . 2019-12-00. Pubmed ID: 31794887; DOI: 10.1016/j.scr.2019.101638 GIBHe001-A 2019-12-00 2019-12-00 PubMed: 31794887 DOI: 10.1016/j.scr.2019.101638Associated cell lines:
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Valerio LSA, Sugaya K
Xeno- and transgene-free reprogramming of mesenchymal stem cells toward the cells expressing neural markers using exosome treatments
Valerio LSA et al. Xeno- and transgene-free reprogramming of mesenchymal stem cells toward the cells expressing neural markers using exosome treatments. . 2020-00-00. Pubmed ID: 33048978; DOI: 10.1371/journal.pone.0240469; PMC: PMC7553345 GZHMUi001-A 2020-00-00 2020-00-00 PubMed: 33048978 DOI: 10.1371/journal.pone.0240469Associated cell lines:
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Sharma R, Smits IPM, De La Vega L, Lee C, Willerth SM
3D Bioprinting Pluripotent Stem Cell Derived Neural Tissues Using a Novel Fibrin Bioink Containing Drug Releasing Microspheres
Sharma R et al. 3D Bioprinting Pluripotent Stem Cell Derived Neural Tissues Using a Novel Fibrin Bioink Containing Drug Releasing Microspheres. . 2020-00-00. Pubmed ID: 32117936; DOI: 10.3389/fbioe.2020.00057; PMC: PMC7026266 IBMSi012-A 2020-00-00 2020-00-00 PubMed: 32117936 DOI: 10.3389/fbioe.2020.00057Associated cell lines:
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Frew J, Wu X, Hsiung GY, Feldman HH, Mackenzie IR, Nygaard HB
Generation of an induced pluripotent stem cell line (UBCi001-A) from a presymptomatic individual carrying the R418X progranulin gene mutation
Frew J et al. Generation of an induced pluripotent stem cell line (UBCi001-A) from a presymptomatic individual carrying the R418X progranulin gene mutation. . 2019-12-00. Pubmed ID: 31707213; DOI: 10.1016/j.scr.2019.101582 UBCi001-A 2019-12-00 2019-12-00 PubMed: 31707213 DOI: 10.1016/j.scr.2019.101582Associated cell lines:
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Ding Y, Marcó de la Cruz B, Xia Y, Liu M, Lu Y, McInerney V, Krawczyk J, Lynch SA, Howard L, O'Brien T, Gallagher L, Shen S
Derivation of familial iPSC lines from three ASD patients carrying NRXN1α(+/-) and two controls (NUIGi022-A, NUIGi022-B; NUIGi023-A, NUIGi023-B; NUIGi025-A, NUIGi025-B; NUIGi024-A, NUIGi024-B; NUIGi026-A, NUIGi026-B)
Ding Y et al. Derivation of familial iPSC lines from three ASD patients carrying NRXN1α(+/-) and two controls (NUIGi022-A, NUIGi022-B; NUIGi023-A, NUIGi023-B; NUIGi025-A, NUIGi025-B; NUIGi024-A, NUIGi024-B; NUIGi026-A, NUIGi026-B). . 2019-12-00. Pubmed ID: 31759289; DOI: 10.1016/j.scr.2019.101653 NUIGi022-ANUIGi023-ANUIGi024-ANUIGi025-ANUIGi026-ANUIGi022-BNUIGi024-BNUIGi025-BNUIGi026-BNUIGi023-B 2019-12-00 2019-12-00 PubMed: 31759289 DOI: 10.1016/j.scr.2019.101653Associated cell lines:
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Hu M, Cherkaoui I, Misra S, Rutter GA
Functional Genomics in Pancreatic β Cells: Recent Advances in Gene Deletion and Genome Editing Technologies for Diabetes Research
Hu M et al. Functional Genomics in Pancreatic β Cells: Recent Advances in Gene Deletion and Genome Editing Technologies for Diabetes Research. . 2020-00-00. Pubmed ID: 33162936; DOI: 10.3389/fendo.2020.576632; PMC: PMC7580382 KSCBi005-AKSCBi005-A-3 2020-00-00 2020-00-00 PubMed: 33162936 DOI: 10.3389/fendo.2020.576632Associated cell lines:
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Mishra K, Junday K, Wong CMY, Chan AY, Hesselson S, Muller DW, Iismaa SE, Mehta A, Graham RM
Generation of VCCRIi001-A, a human induced pluripotent stem cell line, from a patient with spontaneous coronary artery dissection
Mishra K et al. Generation of VCCRIi001-A, a human induced pluripotent stem cell line, from a patient with spontaneous coronary artery dissection. . 2019-12-00. Pubmed ID: 31707208; DOI: 10.1016/j.scr.2019.101584 VCCRIi001-A 2019-12-00 2019-12-00 PubMed: 31707208 DOI: 10.1016/j.scr.2019.101584Associated cell lines:
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Dulovic-Mahlow M, Lukomska A, Diaw SH, Balck A, Borsche M, Grütz K, Lenz I, Rudolph F, Lohmann K, Klein C, Seibler P
Generation and characterization of human-derived iPSC lines from three pairs of monozygotic twins discordant for Parkinson's disease
Dulovic-Mahlow M et al. Generation and characterization of human-derived iPSC lines from three pairs of monozygotic twins discordant for Parkinson's disease. . 2019-12-00. Pubmed ID: 31706098; DOI: 10.1016/j.scr.2019.101629 LUEi006-ALUEi007-ALUEi008-ALUEi009-ALUEi010-ALUEi011-A 2019-12-00 2019-12-00 PubMed: 31706098 DOI: 10.1016/j.scr.2019.101629 -
Lai X, Jiang B, Liu J, Wang Y, Wu G
Generation of an induced pluripotent stem cell line (SYSUi002-A) from a patient with coronary slow flow phenomenon
Lai X et al. Generation of an induced pluripotent stem cell line (SYSUi002-A) from a patient with coronary slow flow phenomenon. . 2019-12-00. Pubmed ID: 31783296; DOI: 10.1016/j.scr.2019.101646 SYSUi002-A 2019-12-00 2019-12-00 PubMed: 31783296 DOI: 10.1016/j.scr.2019.101646Associated cell lines:
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Laowtammathron C, Srisook P, Chingsuwanrote P, Jiamvoraphong N, Waeteekul S, Terbto P, U-Pratya Y, Lorthongpanich C, Issaragrisil S
Derivation of a MUSIi012-A iPSCs from mobilized peripheral blood stem cells
Laowtammathron C et al. Derivation of a MUSIi012-A iPSCs from mobilized peripheral blood stem cells. . 2019-12-00. Pubmed ID: 31669974; DOI: 10.1016/j.scr.2019.101597 MUSIi012-A 2019-12-00 2019-12-00 PubMed: 31669974 DOI: 10.1016/j.scr.2019.101597Associated cell lines:
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Arias-Fuenzalida J, Yu J, Abolhassani H, Du L, Custodio J, Pan-Hammarström Q
Generation of a human induced pluripotent stem cell line (PHAi003) from a primary immunodeficient patient with CD70 mutation
Arias-Fuenzalida J et al. Generation of a human induced pluripotent stem cell line (PHAi003) from a primary immunodeficient patient with CD70 mutation. . 2019-12-00. Pubmed ID: 31678777; DOI: 10.1016/j.scr.2019.101612 PHAi003-APHAi003-B 2019-12-00 2019-12-00 PubMed: 31678777 DOI: 10.1016/j.scr.2019.101612 -
Patterson K, Beers J, Linask KL, Lin Y, Hassanzadeh S, Sack MN, Zou J
Generation of two induced pluripotent stem cell lines (NHLBIi001-A and NHLBIi001-B) from a healthy Caucasian female volunteer with normal cardiac function
Patterson K et al. Generation of two induced pluripotent stem cell lines (NHLBIi001-A and NHLBIi001-B) from a healthy Caucasian female volunteer with normal cardiac function. . 2019-12-00. Pubmed ID: 31733441; DOI: 10.1016/j.scr.2019.101627; PMC: PMC6938693 TRNDi008-ANHLBIi001-ANHLBIi001-B 2019-12-00 2019-12-00 PubMed: 31733441 DOI: 10.1016/j.scr.2019.101627Associated cell lines:
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Ruiz JP, Chen G, Haro Mora JJ, Keyvanfar K, Liu C, Zou J, Beers J, Bloomer H, Qanash H, Uchida N, Tisdale JF, Boehm M, Larochelle A
Robust generation of erythroid and multilineage hematopoietic progenitors from human iPSCs using a scalable monolayer culture system
Ruiz JP et al. Robust generation of erythroid and multilineage hematopoietic progenitors from human iPSCs using a scalable monolayer culture system. . 2019-12-00. Pubmed ID: 31710911; DOI: 10.1016/j.scr.2019.101600; PMC: PMC6953424 TRNDi009-CRTIBDi001-A 2019-12-00 2019-12-00 PubMed: 31710911 DOI: 10.1016/j.scr.2019.101600Associated cell lines:
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Tyagi Nishu, Shamim Uzma, Faruq Mohammed
RNA toxicity in tandem nucleotide repeats mediated neurodegenerative disorders
Tyagi Nishu et al. RNA toxicity in tandem nucleotide repeats mediated neurodegenerative disorders. . 2020-00-00. DOI: 10.1016/b978-0-12-817193-6.00009-1 IGIBi002-AIGIBi003-AIGIBi004-A 2020-00-00 2020-00-00 DOI: 10.1016/b978-0-12-817193-6.00009-1Associated cell lines:
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Martins GLS, Paredes BD, Sampaio GLA, Nonaka CKV, da Silva KN, Allahdadi KJ, França LSA, Soares MBP, Dos Santos RR, Souza BSF
Generation of human iPS cell line CBTCi001-A from dermal fibroblasts obtained from a healthy donor
Martins GLS et al. Generation of human iPS cell line CBTCi001-A from dermal fibroblasts obtained from a healthy donor. . 2019-12-00. Pubmed ID: 31706097; DOI: 10.1016/j.scr.2019.101630 CBTCi001-A 2019-12-00 2019-12-00 PubMed: 31706097 DOI: 10.1016/j.scr.2019.101630Associated cell lines:
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Zhang L, Xu M, Liu G, Wu R, Meng S, Xiahou K, Jiang N, Zhang Y, Zhou W
Generation of induced pluripotent stem cell line (IPTi001-A) from a 62-year old sporadic Alzheimer's disease patient with APOE3 (ε3/ε3) genotype
Zhang L et al. Generation of induced pluripotent stem cell line (IPTi001-A) from a 62-year old sporadic Alzheimer's disease patient with APOE3 (ε3/ε3) genotype. . 2019-12-00. Pubmed ID: 31689594; DOI: 10.1016/j.scr.2019.101589 IPTi001-A 2019-12-00 2019-12-00 PubMed: 31689594 DOI: 10.1016/j.scr.2019.101589Associated cell lines:
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Di Lascio S, Benfante R, Cardani S, Fornasari D
Research Advances on Therapeutic Approaches to Congenital Central Hypoventilation Syndrome (CCHS)
Di Lascio S et al. Research Advances on Therapeutic Approaches to Congenital Central Hypoventilation Syndrome (CCHS). . 2020-00-00. Pubmed ID: 33510615; DOI: 10.3389/fnins.2020.615666; PMC: PMC7835644 BGUi004-ABGUi005-A 2020-00-00 2020-00-00 PubMed: 33510615 DOI: 10.3389/fnins.2020.615666 -
Mohammadi Nazanin A., Freude Kristine, Haukedal Henriette, Tümer Zeynep, Møller Rikke S.
Human induced pluripotent cells in personalized treatment of monogenic epilepsies
Mohammadi Nazanin A. et al. Human induced pluripotent cells in personalized treatment of monogenic epilepsies. . 2020-00-00. DOI: 10.20517/jtgg.2020.29 UKWNLi001-A 2020-00-00 2020-00-00 DOI: 10.20517/jtgg.2020.29Associated cell lines:
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Seshagiri PB, Vani V
Research on early mammalian development in India
Seshagiri PB et al. Research on early mammalian development in India. . 2020-00-00. Pubmed ID: 32658999; DOI: 10.1387/ijdb.190189ps CSCRi005-A 2020-00-00 2020-00-00 PubMed: 32658999 DOI: 10.1387/ijdb.190189psAssociated cell lines:
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So S, Lee Y, Choi J, Kang S, Lee JY, Hwang J, Shin J, Dutton JR, Seo EJ, Lee BH, Kim CJ, Mitalipov S, Oh SJ, Kang E
The Rho-associated kinase inhibitor fasudil can replace Y-27632 for use in human pluripotent stem cell research
So S et al. The Rho-associated kinase inhibitor fasudil can replace Y-27632 for use in human pluripotent stem cell research. . 2020-00-00. Pubmed ID: 32396545; DOI: 10.1371/journal.pone.0233057; PMC: PMC7217428 VRFi001-A 2020-00-00 2020-00-00 PubMed: 32396545 DOI: 10.1371/journal.pone.0233057Associated cell lines:
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Yang Y, Wang J, Liang Q, Wang Y, Chen X, Zhang Q, Na S, Liu Y, Yan T, Hang C, Zhu Y
PHACTR1 is associated with disease progression in Chinese Moyamoya disease
Yang Y et al. PHACTR1 is associated with disease progression in Chinese Moyamoya disease. . 2020-00-00. Pubmed ID: 32411507; DOI: 10.7717/peerj.8841; PMC: PMC7207206 CSCRMi001-A 2020-00-00 2020-00-00 PubMed: 32411507 DOI: 10.7717/peerj.8841Associated cell lines:
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Taghizadeh S, Jones MR, Olmer R, Ulrich S, Danopoulos S, Shen C, Chen C, Wilhelm J, Martin U, Chen C, Al Alam D, Bellusci S
Fgf10 Signaling-Based Evidence for the Existence of an Embryonic Stage Distinct From the Pseudoglandular Stage During Mouse Lung Development
Taghizadeh S et al. Fgf10 Signaling-Based Evidence for the Existence of an Embryonic Stage Distinct From the Pseudoglandular Stage During Mouse Lung Development. . 2020-00-00. Pubmed ID: 33195211; DOI: 10.3389/fcell.2020.576604; PMC: PMC7642470 MHHi006-AMHHi006-A-2 2020-00-00 2020-00-00 PubMed: 33195211 DOI: 10.3389/fcell.2020.576604Associated cell lines:
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Cheung Hoi-Hung, Rennert Owen M.
Werner syndrome induced pluripotent stem cells, a study of pathologic aging
Cheung Hoi-Hung et al. Werner syndrome induced pluripotent stem cells, a study of pathologic aging. . 2020-00-00. DOI: 10.1016/b978-0-12-822227-0.00013-2 REGUi003-A 2020-00-00 2020-00-00 DOI: 10.1016/b978-0-12-822227-0.00013-2Associated cell lines:
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Wang AYL, Loh CYY
Episomal Induced Pluripotent Stem Cells: Functional and Potential Therapeutic Applications
Wang AYL et al. Episomal Induced Pluripotent Stem Cells: Functional and Potential Therapeutic Applications. . 2019-12-00. Pubmed ID: 31722555; DOI: 10.1177/0963689719886534; PMC: PMC7016470 UNIPDi001-ATUSMi001-ANCCSi002-ATUSMi003-AUNIPDi003-ATUSMi004-ATUSMi005-AMUSIi004-AHIHCNi002-AHIHCNi003-AFUi002-AIBPi002-AIMEDEAi004-AIMEDEAi004-BCSi001-ANCCSi004-ATUSMi007-ATUSMi008-A 2019-12-00 2019-12-00 PubMed: 31722555 DOI: 10.1177/0963689719886534 -
Zhang J, Wei L, Chen D, Feng L, Wu C, Wang R, Li X
Generation of an integration-free induced pluripotent stem cell (iPSC) line (ZZUNEUi003-A) from a Wilson's disease patient harboring a homozygous R778L mutation in ATP7B gene
Zhang J et al. Generation of an integration-free induced pluripotent stem cell (iPSC) line (ZZUNEUi003-A) from a Wilson's disease patient harboring a homozygous R778L mutation in ATP7B gene. . 2019-12-00. Pubmed ID: 31783295; DOI: 10.1016/j.scr.2019.101664 ZZUNEUi003-A 2019-12-00 2019-12-00 PubMed: 31783295 DOI: 10.1016/j.scr.2019.101664Associated cell lines:
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Valenti MT, Serena M, Carbonare LD, Zipeto D
CRISPR/Cas system: An emerging technology in stem cell research
Valenti MT et al. CRISPR/Cas system: An emerging technology in stem cell research. . 2019-11-26. Pubmed ID: 31768221; DOI: 10.4252/wjsc.v11.i11.937; PMC: PMC6851009 CSSi002-A 2019-11-26 2019-11-26 PubMed: 31768221 DOI: 10.4252/wjsc.v11.i11.937Associated cell lines:
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Heshusius S, Heideveld E, Burger P, Thiel-Valkhof M, Sellink E, Varga E, Ovchynnikova E, Visser A, Martens JHA, von Lindern M, van den Akker E
Large-scale in vitro production of red blood cells from human peripheral blood mononuclear cells
Heshusius S et al. Large-scale in vitro production of red blood cells from human peripheral blood mononuclear cells. . 2019-11-12. Pubmed ID: 31698463; DOI: 10.1182/bloodadvances.2019000689; PMC: PMC6855111 SANi005-A 2019-11-12 2019-11-12 PubMed: 31698463 DOI: 10.1182/bloodadvances.2019000689Associated cell lines:
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Brodehl A, Pour Hakimi SA, Stanasiuk C, Ratnavadivel S, Hendig D, Gaertner A, Gerull B, Gummert J, Paluszkiewicz L, Milting H
Restrictive Cardiomyopathy is Caused by a Novel Homozygous Desmin (DES) Mutation p.Y122H Leading to a Severe Filament Assembly Defect
Brodehl A et al. Restrictive Cardiomyopathy is Caused by a Novel Homozygous Desmin (DES) Mutation p.Y122H Leading to a Severe Filament Assembly Defect. . 2019-11-11. Pubmed ID: 31718026; DOI: 10.3390/genes10110918; PMC: PMC6896098 UKKi011-A 2019-11-11 2019-11-11 PubMed: 31718026 DOI: 10.3390/genes10110918Associated cell lines:
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El-Battrawy I, Müller J, Zhao Z, Cyganek L, Zhong R, Zhang F, Kleinsorge M, Lan H, Li X, Xu Q, Huang M, Liao Z, Moscu-Gregor A, Albers S, Dinkel H, Lang S, Diecke S, Zimmermann W, Utikal J, Wieland T, Borggrefe M, Zhou X, Akin I.
Studying Brugada Syndrome With an SCN1B Variants in Human-Induced Pluripotent Stem Cell-Derived Cardiomyocytes.
El-Battrawy I et al. Studying Brugada Syndrome With an SCN1B Variants in Human-Induced Pluripotent Stem Cell-Derived Cardiomyocytes. . 2019-11-01. UMGi124-AUMGi128-A 2019-11-01 2019-11-01 -
Ren C, Wang F, Guan LN, Cheng XY, Zhang CY, Geng DQ, Liu CF
A compendious summary of Parkinson's disease patient-derived iPSCs in the first decade
Ren C et al. A compendious summary of Parkinson's disease patient-derived iPSCs in the first decade. . 2019-11-00. Pubmed ID: 31930086; DOI: 10.21037/atm.2019.11.16; PMC: PMC6944564 ZZUi007-A 2019-11-00 2019-11-00 PubMed: 31930086 DOI: 10.21037/atm.2019.11.16Associated cell lines:
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Huang CY, Liu CL, Ting CY, Chiu YT, Cheng YC, Nicholson MW, Hsieh PCH
Human iPSC banking: barriers and opportunities
Huang CY et al. Human iPSC banking: barriers and opportunities. . 2019-10-28. Pubmed ID: 31660969; DOI: 10.1186/s12929-019-0578-x; PMC: PMC6819403 KSCBi003-A 2019-10-28 2019-10-28 PubMed: 31660969 DOI: 10.1186/s12929-019-0578-xAssociated cell lines:
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Miklas JW, Clark E, Levy S, Detraux D, Leonard A, Beussman K, Showalter MR, Smith AT, Hofsteen P, Yang X, Macadangdang J, Manninen T, Raftery D, Madan A, Suomalainen A, Kim DH, Murry CE, Fiehn O, Sniadecki NJ, Wang Y, Ruohola-Baker H
TFPa/HADHA is required for fatty acid beta-oxidation and cardiolipin re-modeling in human cardiomyocytes
Miklas JW et al. TFPa/HADHA is required for fatty acid beta-oxidation and cardiolipin re-modeling in human cardiomyocytes. . 2019-10-11. Pubmed ID: 31604922; DOI: 10.1038/s41467-019-12482-1; PMC: PMC6789043 RUESe002-A 2019-10-11 2019-10-11 PubMed: 31604922 DOI: 10.1038/s41467-019-12482-1Associated cell lines:
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Takahashi M, Yamazaki S
Generation of a human induced pluripotent stem cell line, IMSUTi002-A-1, harboring the leukemia-specific fusion gene ETV6-RUNX1
Takahashi M et al. Generation of a human induced pluripotent stem cell line, IMSUTi002-A-1, harboring the leukemia-specific fusion gene ETV6-RUNX1. . 2019-10-00. Pubmed ID: 31476588; DOI: 10.1016/j.scr.2019.101546 IMSUTi002-AIMSUTi002-A-1 2019-10-00 2019-10-00 PubMed: 31476588 DOI: 10.1016/j.scr.2019.101546Associated cell lines:
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Isasi R, Namorado J, Mah N, Bultjer N, Kurtz A
A pathway for attesting ethical provenance of cell lines: Lessons from the European human pluripotent stem cell registry (hPSC(reg))
Isasi R et al. A pathway for attesting ethical provenance of cell lines: Lessons from the European human pluripotent stem cell registry (hPSC(reg)). . 2019-10-00. Pubmed ID: 31450190; DOI: 10.1016/j.scr.2019.101539 SDQLCHi002-A 2019-10-00 2019-10-00 PubMed: 31450190 DOI: 10.1016/j.scr.2019.101539Associated cell lines:
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Nikitina T. V., Kashevarova A. A., Lebedev I. N.
Chromosomal Instability and Karyotype Correction in Human Induced Pluripotent Stem Cells
Nikitina T. V. et al. Chromosomal Instability and Karyotype Correction in Human Induced Pluripotent Stem Cells. . 2019-10-00. DOI: 10.1134/s1022795419100090 IMGTi001-AIMGTi001-BIMGTi003-A 2019-10-00 2019-10-00 DOI: 10.1134/s1022795419100090Associated cell lines:
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Zhang H, Ma Y, Yan B, Yang X, Li Y, Guan J, Dong R, Liu Y, Gai Z
Establishment of a human induced pluripotent stem cell line (SDQLCHi005-A) from a patient with mastocytosis carrying heterozygous mutation in KIT gene
Zhang H et al. Establishment of a human induced pluripotent stem cell line (SDQLCHi005-A) from a patient with mastocytosis carrying heterozygous mutation in KIT gene. . 2019-10-00. Pubmed ID: 31522012; DOI: 10.1016/j.scr.2019.101565 SDQLCHi005-A 2019-10-00 2019-10-00 PubMed: 31522012 DOI: 10.1016/j.scr.2019.101565Associated cell lines:
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Ma Y, Zhang H, Yang X, Li Y, Guan J, Lv Y, Li H, Liu Y, Gai Z
Establishment of a human induced pluripotent stem cell line (SDQLCHi004-A) from a patient with nemaline myopathy-4 disease carrying heterozygous mutation in TPM2 gene
Ma Y et al. Establishment of a human induced pluripotent stem cell line (SDQLCHi004-A) from a patient with nemaline myopathy-4 disease carrying heterozygous mutation in TPM2 gene. . 2019-10-00. Pubmed ID: 31526942; DOI: 10.1016/j.scr.2019.101559 SDQLCHi004-A 2019-10-00 2019-10-00 PubMed: 31526942 DOI: 10.1016/j.scr.2019.101559Associated cell lines:
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Ma Y, Zhang H, Yang X, Li Y, Guan J, Zhang K, Huang Y, Pan G, Gai Z, Liu Y
Generation of two induced pluripotent stem cell lines from patients with unbalanced translocation (3;22)
Ma Y et al. Generation of two induced pluripotent stem cell lines from patients with unbalanced translocation (3;22). . 2019-10-00. Pubmed ID: 31472451; DOI: 10.1016/j.scr.2019.101545 SDQLCHi001-ASDQLCHi002-A 2019-10-00 2019-10-00 PubMed: 31472451 DOI: 10.1016/j.scr.2019.101545Associated cell lines:
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Han HJ, Han HW, Seo HH, Kim JH
Generation of a KSCBi005-A-5(TLR8KO-A10) homozygous knockout human induced pluripotent stem cell line using CRISPR/Cas9
Han HJ et al. Generation of a KSCBi005-A-5(TLR8KO-A10) homozygous knockout human induced pluripotent stem cell line using CRISPR/Cas9. . 2019-10-00. Pubmed ID: 31526944; DOI: 10.1016/j.scr.2019.101561 KSCBi005-AKSCBi005-A-5 2019-10-00 2019-10-00 PubMed: 31526944 DOI: 10.1016/j.scr.2019.101561Associated cell lines:
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Cheng YF, Chan YH, Hu CJ, Lu YC, Saeki T, Hosoya M, Saegusa C, Fujioka M, Okano H, Weng SM, Hsu CJ, Chang KH, Wu CC
Generation of a human iPS cell line (CGMH.SLC26A4919-2) from a Pendred syndrome patient carrying SLC26A4 c.919-2A>G splice-site mutation
Cheng YF et al. Generation of a human iPS cell line (CGMH.SLC26A4919-2) from a Pendred syndrome patient carrying SLC26A4 c.919-2A>G splice-site mutation. . 2019-10-00. Pubmed ID: 31415960; DOI: 10.1016/j.scr.2019.101524 CGMHi001-A 2019-10-00 2019-10-00 PubMed: 31415960 DOI: 10.1016/j.scr.2019.101524Associated cell lines:
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Bidollari E, Rotundo G, Altieri F, Amicucci M, Wiquel D, Ferrari D, Goldoni M, Bernardini L, Consoli F, De Luca A, Fanelli S, Lamorte G, D'Agruma L, Vescovi AL, Squitieri F, Rosati J
Generation of induced pluripotent stem cell line CSSi008-A (4698) from a patient affected by advanced stage of Dentato-Rubral-Pallidoluysian atrophy (DRPLA)
Bidollari E et al. Generation of induced pluripotent stem cell line CSSi008-A (4698) from a patient affected by advanced stage of Dentato-Rubral-Pallidoluysian atrophy (DRPLA). . 2019-10-00. Pubmed ID: 31493762; DOI: 10.1016/j.scr.2019.101551 CSSi008-A 2019-10-00 2019-10-00 PubMed: 31493762 DOI: 10.1016/j.scr.2019.101551Associated cell lines:
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Jelinkova S, Markova L, Pesl M, Valáškova I, Makaturová E, Jurikova L, Vondracek P, Lacampagne A, Dvorak P, Meli AC, Rotrekl V
Generation of two Duchenne muscular dystrophy patient-specific induced pluripotent stem cell lines DMD02 and DMD03 (MUNIi001-A and MUNIi003-A)
Jelinkova S et al. Generation of two Duchenne muscular dystrophy patient-specific induced pluripotent stem cell lines DMD02 and DMD03 (MUNIi001-A and MUNIi003-A). . 2019-10-00. Pubmed ID: 31526943; DOI: 10.1016/j.scr.2019.101562 MUNIi001-AMUNIi003-A 2019-10-00 2019-10-00 PubMed: 31526943 DOI: 10.1016/j.scr.2019.101562Associated cell lines:
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Rodríguez-Traver E, Rodríguez C, Díaz-Guerra E, Arenas F, Araúzo-Bravo M, Orera M, Kulisevsky J, Moratalla R, Vicario C
Generation of an integration-free iPSC line, ICCSICi005-A, derived from a Parkinson's disease patient carrying the L444P mutation in the GBA1 gene
Rodríguez-Traver E et al. Generation of an integration-free iPSC line, ICCSICi005-A, derived from a Parkinson's disease patient carrying the L444P mutation in the GBA1 gene. . 2019-10-00. Pubmed ID: 31539859; DOI: 10.1016/j.scr.2019.101578 ICCSICi005-A 2019-10-00 2019-10-00 PubMed: 31539859 DOI: 10.1016/j.scr.2019.101578Associated cell lines:
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Cerrada V, García-López M, Moreno-Izquierdo A, Villaverde C, Zurita O, Martin-Merida MI, Arenas J, Ayuso C, Gallardo ME
Derivation of a human DOA iPSC line, IISHDOi006-A, with a mutation in the ACO2 gene: c.1999G>A; p.Glu667Lys
Cerrada V et al. Derivation of a human DOA iPSC line, IISHDOi006-A, with a mutation in the ACO2 gene: c.1999G>A; p.Glu667Lys. . 2019-10-00. Pubmed ID: 31509793; DOI: 10.1016/j.scr.2019.101566 IISHDOi006-A 2019-10-00 2019-10-00 PubMed: 31509793 DOI: 10.1016/j.scr.2019.101566Associated cell lines:
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Lee Y, Choi HY, Kwon A, Park H, Park M, Kim YO, Kwak S, Koo SK
Generation of a NESTIN-EGFP reporter human induced pluripotent stem cell line, KSCBi005-A-1, using CRISPR/Cas9 nuclease
Lee Y et al. Generation of a NESTIN-EGFP reporter human induced pluripotent stem cell line, KSCBi005-A-1, using CRISPR/Cas9 nuclease. . 2019-10-00. Pubmed ID: 31499408; DOI: 10.1016/j.scr.2019.101554 KSCBi005-AKSCBi005-A-1 2019-10-00 2019-10-00 PubMed: 31499408 DOI: 10.1016/j.scr.2019.101554Associated cell lines:
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Li Y, Zhang H, Yan B, Ma Y, Yang X, Guan J, Lv Y, Gao M, Ma J, Gai Z, Liu Y
An induced pluripotent stem cell line (SDQLCHi006-A) derived from a patient with maple syrup urine disease type Ib carrying compound heterozygous mutations of p.R168C and p.T322I in BCKDHB gene
Li Y et al. An induced pluripotent stem cell line (SDQLCHi006-A) derived from a patient with maple syrup urine disease type Ib carrying compound heterozygous mutations of p.R168C and p.T322I in BCKDHB gene. . 2019-10-00. Pubmed ID: 31610500; DOI: 10.1016/j.scr.2019.101579 SDQLCHi006-A 2019-10-00 2019-10-00 PubMed: 31610500 DOI: 10.1016/j.scr.2019.101579Associated cell lines:
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Yang M, Liu M, Vajda A, O'Brien T, Henshall D, Hardiman O, Shen S
Generation of six induced pluripotent stem cell (iPSC) lines from two patients with amyotrophic lateral sclerosis (NUIGi043-A, NUIGi043-B, NUIGi043-C, NUIGi044-A, NUIGi044-B, NUIGi044-C)
Yang M et al. Generation of six induced pluripotent stem cell (iPSC) lines from two patients with amyotrophic lateral sclerosis (NUIGi043-A, NUIGi043-B, NUIGi043-C, NUIGi044-A, NUIGi044-B, NUIGi044-C). . 2019-10-00. Pubmed ID: 31514057; DOI: 10.1016/j.scr.2019.101558 NUIGi043-ANUIGi043-BNUIGi043-CNUIGi044-ANUIGi044-BNUIGi044-C 2019-10-00 2019-10-00 PubMed: 31514057 DOI: 10.1016/j.scr.2019.101558Associated cell lines:
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He L, Ye W, Chen Z, Wang C, Zhao H, Li S, Peng L, Han X, Zhou T, Li Z, Tang B, Jiang H
Generation of an induced pluripotent stem cell line (XHCSUi001-A) from urine cells of a patient with spinocerebellar ataxia type 3
He L et al. Generation of an induced pluripotent stem cell line (XHCSUi001-A) from urine cells of a patient with spinocerebellar ataxia type 3. . 2019-10-00. Pubmed ID: 31491691; DOI: 10.1016/j.scr.2019.101555 CSUXHi001-A 2019-10-00 2019-10-00 PubMed: 31491691 DOI: 10.1016/j.scr.2019.101555Associated cell lines:
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Bax M, Balez R, Muñoz SS, Do-Ha D, Stevens CH, Berg T, Cabral-da-Silva MC, Engel M, Nicholson G, Yang S, Blair IP, Ooi L
Generation and characterization of a human induced pluripotent stem cell line UOWi005-A from dermal fibroblasts derived from a CCNF(S621G) familial amyotrophic lateral sclerosis patient using mRNA reprogramming
Bax M et al. Generation and characterization of a human induced pluripotent stem cell line UOWi005-A from dermal fibroblasts derived from a CCNF(S621G) familial amyotrophic lateral sclerosis patient using mRNA reprogramming. . 2019-10-00. Pubmed ID: 31445393; DOI: 10.1016/j.scr.2019.101530 UOWi005-A 2019-10-00 2019-10-00 PubMed: 31445393 DOI: 10.1016/j.scr.2019.101530Associated cell lines:
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Rovina D, Castiglioni E, Farini A, Bellichi M, Gervasini C, Paganini S, Di Segni M, Santoro R, Torrente Y, Pompilio G, Gowran A
Establishment of a Duchenne muscular dystrophy patient-derived induced pluripotent stem cell line carrying a deletion of exons 51-53 of the dystrophin gene (CCMi003-A)
Rovina D et al. Establishment of a Duchenne muscular dystrophy patient-derived induced pluripotent stem cell line carrying a deletion of exons 51-53 of the dystrophin gene (CCMi003-A). . 2019-10-00. Pubmed ID: 31465894; DOI: 10.1016/j.scr.2019.101544 CCMi003-A 2019-10-00 2019-10-00 PubMed: 31465894 DOI: 10.1016/j.scr.2019.101544Associated cell lines:
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Díaz-Guerra E, Oria-Muriel MA, Moreno-Jiménez EP, de Rojasb I, Rodríguez C, Rodríguez-Traver E, Orera M, Hernándezb I, Ruizb A, Vicario C
Generation of an integration-free iPSC line, ICCSICi006-A, derived from a male Alzheimer's disease patient carrying the PSEN1-G206D mutation
Díaz-Guerra E et al. Generation of an integration-free iPSC line, ICCSICi006-A, derived from a male Alzheimer's disease patient carrying the PSEN1-G206D mutation. . 2019-10-00. Pubmed ID: 31627126; DOI: 10.1016/j.scr.2019.101574 ICCSICi006-A 2019-10-00 2019-10-00 PubMed: 31627126 DOI: 10.1016/j.scr.2019.101574Associated cell lines:
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Teinert J, Behne R, D'Amore A, Wimmer M, Dwyer S, Chen T, Buttermore ED, Chen IP, Sahin M, Ebrahimi-Fakhari D
Generation and characterization of six human induced pluripotent stem cell lines (iPSC) from three families with AP4B1-associated hereditary spastic paraplegia (SPG47)
Teinert J et al. Generation and characterization of six human induced pluripotent stem cell lines (iPSC) from three families with AP4B1-associated hereditary spastic paraplegia (SPG47). . 2019-10-00. Pubmed ID: 31525725; DOI: 10.1016/j.scr.2019.101575; PMC: PMC7269118 BCHNEUi001-ABCHNEUi002-ABCHNEUi003-ABCHNEUi004-ABCHNEUi005-ABCHNEUi006-A 2019-10-00 2019-10-00 PubMed: 31525725 DOI: 10.1016/j.scr.2019.101575Associated cell lines:
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Zhang Y, Hu W, Ma K, Zhang C, Fu X
Reprogramming of Keratinocytes as Donor or Target Cells Holds Great Promise for Cell Therapy and Regenerative Medicine
Zhang Y et al. Reprogramming of Keratinocytes as Donor or Target Cells Holds Great Promise for Cell Therapy and Regenerative Medicine. . 2019-10-00. Pubmed ID: 31197578; DOI: 10.1007/s12015-019-09900-8 MUSIi006-A 2019-10-00 2019-10-00 PubMed: 31197578 DOI: 10.1007/s12015-019-09900-8Associated cell lines:
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Li S, Zhao H, Huang R, He L, Tian C, Huang H, Han X, Tang F, Lin Z, Deng S, Zhou J, Li Z
Generation of iPSC line (GIBHi001-A) from a patient with autism spectrum disorder
Li S et al. Generation of iPSC line (GIBHi001-A) from a patient with autism spectrum disorder. . 2019-10-00. Pubmed ID: 31520889; DOI: 10.1016/j.scr.2019.101571 GIBHi001-A 2019-10-00 2019-10-00 PubMed: 31520889 DOI: 10.1016/j.scr.2019.101571Associated cell lines:
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Shivaraj A, Parveen S
Generation of integration free human iPSC line SORMi002-A from neonatal foreskin fibroblasts
Shivaraj A et al. Generation of integration free human iPSC line SORMi002-A from neonatal foreskin fibroblasts. . 2019-10-00. Pubmed ID: 31454679; DOI: 10.1016/j.scr.2019.101534 SORMi002-A 2019-10-00 2019-10-00 PubMed: 31454679 DOI: 10.1016/j.scr.2019.101534Associated cell lines:
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Domingo-Prim J, Riera M, Abad-Morales V, Ruiz-Nogales S, Corcostegui B, Pomares E
Generation of Best disease-derived induced pluripotent stem cell line (FRIMOi006-A) carrying a novel dominant mutation in BEST1 gene
Domingo-Prim J et al. Generation of Best disease-derived induced pluripotent stem cell line (FRIMOi006-A) carrying a novel dominant mutation in BEST1 gene. . 2019-10-00. Pubmed ID: 31518904; DOI: 10.1016/j.scr.2019.101570 FRIMOi006-A 2019-10-00 2019-10-00 PubMed: 31518904 DOI: 10.1016/j.scr.2019.101570Associated cell lines:
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Chiu CC, Wang HL, Weng YH, Chen RS, Chen CM, Yeh TH, Lu CS, Chen YJ, Liu YC, Huang YZ, Chang KH
Generation of induced pluripotent stem cells from a young-onset Parkinson's disease patient carrying the compound heterozygous PLA2G6 p.D331Y/p.M358IfsX mutations
Chiu CC et al. Generation of induced pluripotent stem cells from a young-onset Parkinson's disease patient carrying the compound heterozygous PLA2G6 p.D331Y/p.M358IfsX mutations. . 2019-10-00. Pubmed ID: 31493761; DOI: 10.1016/j.scr.2019.101552 CGMHi002-A 2019-10-00 2019-10-00 PubMed: 31493761 DOI: 10.1016/j.scr.2019.101552Associated cell lines:
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Zeng R, Sidik H, Robinson KS, Zhong FL, Reversade B, Pouladi MA
Generation of four H1 hESC sublines carrying a hemizygous knock-out/mutant MECP2
Zeng R et al. Generation of four H1 hESC sublines carrying a hemizygous knock-out/mutant MECP2. . 2019-10-00. Pubmed ID: 31450191; DOI: 10.1016/j.scr.2019.101533 WAe001-A-25WAe001-A-26WAe001-A-27WAe001-A-28 2019-10-00 2019-10-00 PubMed: 31450191 DOI: 10.1016/j.scr.2019.101533Associated cell lines:
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van der Wal E, den Hamer B, van der Vliet PJ, Tok M, Brands T, Eussen B, Lemmers RJLF, Freund C, de Klein A, Buijsen RAM, van Roon-Mom WMC, Tawil R, van der Maarel SM, de Greef JC
Generation of genetically matched hiPSC lines from two mosaic facioscapulohumeral dystrophy type 1 patients
van der Wal E et al. Generation of genetically matched hiPSC lines from two mosaic facioscapulohumeral dystrophy type 1 patients. . 2019-10-00. Pubmed ID: 31518905; DOI: 10.1016/j.scr.2019.101560 LUMCi002-ALUMCi003-ALUMCi011-ALUMCi011-BLUMCi012-ALUMCi012-B 2019-10-00 2019-10-00 PubMed: 31518905 DOI: 10.1016/j.scr.2019.101560Associated cell lines:
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Yang X, Zhou T, Zhang H, Li Y, Dong R, Liu N, Pan G, Liu Y, Gai Z
Generation of an induced pluripotent stem cell line (SDQLCHi008-A) from a patient with ASD and DD carrying an 830 kb de novo deletion at chr7q11.22 including the exon 1 of AUTS2 gene
Yang X et al. Generation of an induced pluripotent stem cell line (SDQLCHi008-A) from a patient with ASD and DD carrying an 830 kb de novo deletion at chr7q11.22 including the exon 1 of AUTS2 gene. . 2019-10-00. Pubmed ID: 31505389; DOI: 10.1016/j.scr.2019.101557 SDQLCHi008-A 2019-10-00 2019-10-00 PubMed: 31505389 DOI: 10.1016/j.scr.2019.101557Associated cell lines:
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Fernandes S, Khan N, Kale V, Limaye L
Catalase incorporation in freezing mixture leads to improved recovery of cryopreserved iPSC lines
Fernandes S et al. Catalase incorporation in freezing mixture leads to improved recovery of cryopreserved iPSC lines. . 2019-10-00. Pubmed ID: 31494090; DOI: 10.1016/j.cryobiol.2019.09.003 NCCSi003-A 2019-10-00 2019-10-00 PubMed: 31494090 DOI: 10.1016/j.cryobiol.2019.09.003Associated cell lines:
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Domingo-Prim J, Abad-Morales V, Riera M, Navarro R, Corcostegui B, Pomares E
Generation of an induced pluripotent stem cell line (FRIMOi007-A) derived from an incomplete achromatopsia patient carrying a novel homozygous mutation in PDE6C gene
Domingo-Prim J et al. Generation of an induced pluripotent stem cell line (FRIMOi007-A) derived from an incomplete achromatopsia patient carrying a novel homozygous mutation in PDE6C gene. . 2019-10-00. Pubmed ID: 31520890; DOI: 10.1016/j.scr.2019.101569 FRIMOi007-A 2019-10-00 2019-10-00 PubMed: 31520890 DOI: 10.1016/j.scr.2019.101569Associated cell lines:
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Uysal B, Löffler H, Rosa F, Lerche H, Schwarz N
Generation of an induced pluripotent stem cell (iPSC) line (HIHDNEi003-A) from a patient with developmental and epileptic encephalopathy carrying a KCNA2 (p.Thr374Ala) mutation
Uysal B et al. Generation of an induced pluripotent stem cell (iPSC) line (HIHDNEi003-A) from a patient with developmental and epileptic encephalopathy carrying a KCNA2 (p.Thr374Ala) mutation. . 2019-10-00. Pubmed ID: 31465893; DOI: 10.1016/j.scr.2019.101543 HIHDNEi002-AHIHDNEi003-A 2019-10-00 2019-10-00 PubMed: 31465893 DOI: 10.1016/j.scr.2019.101543Associated cell lines:
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Wallace E, Howard L, Liu M, O'Brien T, Ward D, Shen S, Prendiville T
Long QT Syndrome: Genetics and Future Perspective
Wallace E et al. Long QT Syndrome: Genetics and Future Perspective. . 2019-10-00. Pubmed ID: 31440766; DOI: 10.1007/s00246-019-02151-x; PMC: PMC6785594 PSMi002-APSMi003-A 2019-10-00 2019-10-00 PubMed: 31440766 DOI: 10.1007/s00246-019-02151-x -
Naphade S, Tshilenge KT, Ellerby LM
Modeling Polyglutamine Expansion Diseases with Induced Pluripotent Stem Cells
Naphade S et al. Modeling Polyglutamine Expansion Diseases with Induced Pluripotent Stem Cells. . 2019-10-00. Pubmed ID: 31792895; DOI: 10.1007/s13311-019-00810-8; PMC: PMC6985408 LUMCi002-ALUMCi003-ACHOPi002-ACHOPi003-ALUMCi007-ALUMCi008-AIBCHi001-ACSSi008-ACSUXHi001-A 2019-10-00 2019-10-00 PubMed: 31792895 DOI: 10.1007/s13311-019-00810-8Associated cell lines:
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Alari V, Russo S, Rovina D, Garzo M, Crippa M, Calzari L, Scalera C, Concolino D, Castiglioni E, Giardino D, Prosperi E, Finelli P, Gervasini C, Gowran A, Larizza L
Generation of three iPSC lines (IAIi002, IAIi004, IAIi003) from Rubinstein-Taybi syndrome 1 patients carrying CREBBP non sense c.4435G>T, p.(Gly1479*) and c.3474G>A, p.(Trp1158*) and missense c.4627G>T, p.(Asp1543Tyr) mutations
Alari V et al. Generation of three iPSC lines (IAIi002, IAIi004, IAIi003) from Rubinstein-Taybi syndrome 1 patients carrying CREBBP non sense c.4435G>T, p.(Gly1479*) and c.3474G>A, p.(Trp1158*) and missense c.4627G>T, p.(Asp1543Tyr) mutations. . 2019-10-00. Pubmed ID: 31491690; DOI: 10.1016/j.scr.2019.101553 IAIi002-AIAIi003-AIAIi004-A 2019-10-00 2019-10-00 PubMed: 31491690 DOI: 10.1016/j.scr.2019.101553 -
Han HJ, Seo HH, Han HW, Kim JH
Generation of a TLR7 homozygous knockout human induced pluripotent stem cell line using CRISPR/Cas9
Han HJ et al. Generation of a TLR7 homozygous knockout human induced pluripotent stem cell line using CRISPR/Cas9. . 2019-10-00. Pubmed ID: 31445394; DOI: 10.1016/j.scr.2019.101520 KSCBi005-AKSCBi005-A-4 2019-10-00 2019-10-00 PubMed: 31445394 DOI: 10.1016/j.scr.2019.101520Associated cell lines:
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Huang Z, Zhang D, Chen SC, Thompson JA, McLaren T, Lamey T, De Roach JN, McLenachan S, Chen FK
Generation of three induced pluripotent stem cell lines from an isolated inherited retinal dystrophy patient with RCBTB1 frameshifting mutations
Huang Z et al. Generation of three induced pluripotent stem cell lines from an isolated inherited retinal dystrophy patient with RCBTB1 frameshifting mutations. . 2019-10-00. Pubmed ID: 31494449; DOI: 10.1016/j.scr.2019.101549 LEIi010-BLEIi011-ALEIi011-BLEIi011-C 2019-10-00 2019-10-00 PubMed: 31494449 DOI: 10.1016/j.scr.2019.101549 -
Koike H, Iwasawa K, Ouchi R, Maezawa M, Giesbrecht K, Saiki N, Ferguson A, Kimura M, Thompson WL, Wells JM, Zorn AM, Takebe T
Modelling human hepato-biliary-pancreatic organogenesis from the foregut-midgut boundary
Koike H et al. Modelling human hepato-biliary-pancreatic organogenesis from the foregut-midgut boundary. . 2019-10-00. Pubmed ID: 31554966; DOI: 10.1038/s41586-019-1598-0; PMC: PMC7643931 CUSTOMi001-A 2019-10-00 2019-10-00 PubMed: 31554966 DOI: 10.1038/s41586-019-1598-0Associated cell lines:
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Pandolfi EC, Rojas EJ, Sosa E, Gell JJ, Hunt TJ, Goldsmith S, Fan Y, Silber SJ, Clark AT
Generation of three human induced pluripotent stem cell sublines (MZT04D, MZT04J, MZT04C) for reproductive science research
Pandolfi EC et al. Generation of three human induced pluripotent stem cell sublines (MZT04D, MZT04J, MZT04C) for reproductive science research. . 2019-10-00. Pubmed ID: 31622877; DOI: 10.1016/j.scr.2019.101576 UCLAi001-AUCLAi001-BUCLAi001-C 2019-10-00 2019-10-00 PubMed: 31622877 DOI: 10.1016/j.scr.2019.101576Associated cell lines:
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Engels L, Olmer R, de la Roche J, Göhring G, Ulrich S, Haller R, Martin U, Merkert S
Generation of a CFTR knock-in reporter cell line (MHHi006-A-1) from a human induced pluripotent stem cell line
Engels L et al. Generation of a CFTR knock-in reporter cell line (MHHi006-A-1) from a human induced pluripotent stem cell line. . 2019-10-00. Pubmed ID: 31473565; DOI: 10.1016/j.scr.2019.101542 MHHi006-AMHHi006-A-1 2019-10-00 2019-10-00 PubMed: 31473565 DOI: 10.1016/j.scr.2019.101542Associated cell lines:
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Liu H, Tsui Y, Wang J, Su C, Zheng R, Shao Y, Ni B
Establishment of a Beals syndrome patient-derived human induced pluripotent stem cell line HELPi001-A
Liu H et al. Establishment of a Beals syndrome patient-derived human induced pluripotent stem cell line HELPi001-A. . 2019-10-00. Pubmed ID: 31426022; DOI: 10.1016/j.scr.2019.101535 HELPi001-A 2019-10-00 2019-10-00 PubMed: 31426022 DOI: 10.1016/j.scr.2019.101535Associated cell lines:
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Lanzi G, Masneri S, Ferraro RM, Genova E, Piovani G, Barisani C, Pelin M, Stocco G, Decorti G, Bramuzzo M, Giliani S
Generation of 3 clones of induced pluripotent stem cells (iPSCs) from a patient affected by Crohn's disease
Lanzi G et al. Generation of 3 clones of induced pluripotent stem cells (iPSCs) from a patient affected by Crohn's disease. . 2019-10-00. Pubmed ID: 31536868; DOI: 10.1016/j.scr.2019.101548 UNIBSi005-AUNIBSi005-BUNIBSi005-C 2019-10-00 2019-10-00 PubMed: 31536868 DOI: 10.1016/j.scr.2019.101548Associated cell lines:
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Gridina MM, Nikitina TV, Pristyazhnyuk IE, Kashevarova AA, Lopatkina ME, Vasilyev SA, Nazarenko LP, Lebedev IN, Serov OL
Generation of the induced pluripotent stem cell line, ICAGi002-A, from unaffected carrier megabase scaled duplication involving the CNTN6 gene
Gridina MM et al. Generation of the induced pluripotent stem cell line, ICAGi002-A, from unaffected carrier megabase scaled duplication involving the CNTN6 gene. . 2019-10-00. Pubmed ID: 31518906; DOI: 10.1016/j.scr.2019.101556 ICGi017-A 2019-10-00 2019-10-00 PubMed: 31518906 DOI: 10.1016/j.scr.2019.101556Associated cell lines:
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Egorova PA, Bezprozvanny IB
Molecular Mechanisms and Therapeutics for Spinocerebellar Ataxia Type 2
Egorova PA et al. Molecular Mechanisms and Therapeutics for Spinocerebellar Ataxia Type 2. . 2019-10-00. Pubmed ID: 31435879; DOI: 10.1007/s13311-019-00777-6; PMC: PMC6985344 CHOPi002-ACHOPi003-A 2019-10-00 2019-10-00 PubMed: 31435879 DOI: 10.1007/s13311-019-00777-6Associated cell lines:
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Malerba N, Benzoni P, Squeo GM, Milanesi R, Giannetti F, Sadleir LG, Poke G, Augello B, Croce AI, Barbuti A, Merla G
Generation of the induced human pluripotent stem cell lines CSSi009-A from a patient with a GNB5 pathogenic variant, and CSSi010-A from a CRISPR/Cas9 engineered GNB5 knock-out human cell line
Malerba N et al. Generation of the induced human pluripotent stem cell lines CSSi009-A from a patient with a GNB5 pathogenic variant, and CSSi010-A from a CRISPR/Cas9 engineered GNB5 knock-out human cell line. . 2019-10-00. Pubmed ID: 31479876; DOI: 10.1016/j.scr.2019.101547 CSSi009-ACSSi010-A 2019-10-00 2019-10-00 PubMed: 31479876 DOI: 10.1016/j.scr.2019.101547 -
Hasselmann J, Coburn MA, England W, Figueroa Velez DX, Kiani Shabestari S, Tu CH, McQuade A, Kolahdouzan M, Echeverria K, Claes C, Nakayama T, Azevedo R, Coufal NG, Han CZ, Cummings BJ, Davtyan H, Glass CK, Healy LM, Gandhi SP, Spitale RC, Blurton-Jones M
Development of a Chimeric Model to Study and Manipulate Human Microglia In Vivo
Hasselmann J et al. Development of a Chimeric Model to Study and Manipulate Human Microglia In Vivo. . 2019-09-25. Pubmed ID: 31375314; DOI: 10.1016/j.neuron.2019.07.002; PMC: PMC7138101 BIONi010-CBIONi010-C-7 2019-09-25 2019-09-25 PubMed: 31375314 DOI: 10.1016/j.neuron.2019.07.002Associated cell lines:
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Erkilic N, Gatinois V, Torriano S, Bouret P, Sanjurjo-Soriano C, Luca V, Damodar K, Cereso N, Puechberty J, Sanchez-Alcudia R, Hamel CP, Ayuso C, Meunier I, Pellestor F, Kalatzis V
A Novel Chromosomal Translocation Identified due to Complex Genetic Instability in iPSC Generated for Choroideremia
Erkilic N et al. A Novel Chromosomal Translocation Identified due to Complex Genetic Instability in iPSC Generated for Choroideremia. . 2019-09-11. Pubmed ID: 31514470; DOI: 10.3390/cells8091068; PMC: PMC6770680 INMi001-AINMi002-AINMi003-AINMi004-A 2019-09-11 2019-09-11 PubMed: 31514470 DOI: 10.3390/cells8091068 -
Ramme AP, Koenig L, Hasenberg T, Schwenk C, Magauer C, Faust D, Lorenz AK, Krebs AC, Drewell C, Schirrmann K, Vladetic A, Lin GC, Pabinger S, Neuhaus W, Bois F, Lauster R, Marx U, Dehne EM
Autologous induced pluripotent stem cell-derived four-organ-chip
Ramme AP et al. Autologous induced pluripotent stem cell-derived four-organ-chip. . 2019-09-10. Pubmed ID: 31534781; DOI: 10.2144/fsoa-2019-0065; PMC: PMC6745596 TISSUi001-A 2019-09-10 2019-09-10 PubMed: 31534781 DOI: 10.2144/fsoa-2019-0065Associated cell lines:
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Brodehl A, Ebbinghaus H, Deutsch MA, Gummert J, Gärtner A, Ratnavadivel S, Milting H
Human Induced Pluripotent Stem-Cell-Derived Cardiomyocytes as Models for Genetic Cardiomyopathies
Brodehl A et al. Human Induced Pluripotent Stem-Cell-Derived Cardiomyocytes as Models for Genetic Cardiomyopathies. . 2019-09-06. Pubmed ID: 31489928; DOI: 10.3390/ijms20184381; PMC: PMC6770343 ISMMSi002-BEURACi001-AEURACi002-AEURACi003-AEURACi004-ATRNDi003-A 2019-09-06 2019-09-06 PubMed: 31489928 DOI: 10.3390/ijms20184381Associated cell lines:
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Stelcer E, Kulcenty K, Rucinski M, Jopek K, Richter M, Trzeciak T, Suchorska WM
The Role of MicroRNAs in Early Chondrogenesis of Human Induced Pluripotent Stem Cells (hiPSCs)
Stelcer E et al. The Role of MicroRNAs in Early Chondrogenesis of Human Induced Pluripotent Stem Cells (hiPSCs). . 2019-09-05. Pubmed ID: 31492046; DOI: 10.3390/ijms20184371; PMC: PMC6770352 GPCCi001-A 2019-09-05 2019-09-05 PubMed: 31492046 DOI: 10.3390/ijms20184371Associated cell lines:
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El-Battrawy I, Albers S, Cyganek L, Zhao Z, Lan H, Li X, Xu Q, Kleinsorge M, Huang M, Liao Z, Zhong R, Rudic B, Müller J, Dinkel H, Lang S, Diecke S, Zimmermann WH, Utikal J, Wieland T, Borggrefe M, Zhou X, Akin I
A cellular model of Brugada syndrome with SCN10A variants using human-induced pluripotent stem cell-derived cardiomyocytes
El-Battrawy I et al. A cellular model of Brugada syndrome with SCN10A variants using human-induced pluripotent stem cell-derived cardiomyocytes. . 2019-09-01. Pubmed ID: 31106349; DOI: 10.1093/europace/euz122 UMGi126-A 2019-09-01 2019-09-01 PubMed: 31106349 DOI: 10.1093/europace/euz122Associated cell lines:
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Ahmed M, Marziali LN, Arenas E, Feltri ML, Ffrench-Constant C
Laminin α2 controls mouse and human stem cell behaviour during midbrain dopaminergic neuron development
Ahmed M et al. Laminin α2 controls mouse and human stem cell behaviour during midbrain dopaminergic neuron development. . 2019-08-29. Pubmed ID: 31371375; DOI: 10.1242/dev.172668; PMC: PMC6737905 RCe021-A 2019-08-29 2019-08-29 PubMed: 31371375 DOI: 10.1242/dev.172668Associated cell lines:
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Poulin H, Martineau L, Racine V, Puymirat J, Chahine M
Differentiation of lymphoblastoid-derived iPSCs into functional cardiomyocytes, neurons and myoblasts
Poulin H et al. Differentiation of lymphoblastoid-derived iPSCs into functional cardiomyocytes, neurons and myoblasts. . 2019-08-13. Pubmed ID: 31208718; DOI: 10.1016/j.bbrc.2019.05.176 CHUQi001-ATUSMi001-A 2019-08-13 2019-08-13 PubMed: 31208718 DOI: 10.1016/j.bbrc.2019.05.176Associated cell lines:
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Halloin C, Schwanke K, Löbel W, Franke A, Szepes M, Biswanath S, Wunderlich S, Merkert S, Weber N, Osten F, de la Roche J, Polten F, Christoph Wollert K, Kraft T, Fischer M, Martin U, Gruh I, Kempf H, Zweigerdt R
Continuous WNT Control Enables Advanced hPSC Cardiac Processing and Prognostic Surface Marker Identification in Chemically Defined Suspension Culture
Halloin C et al. Continuous WNT Control Enables Advanced hPSC Cardiac Processing and Prognostic Surface Marker Identification in Chemically Defined Suspension Culture. . 2019-08-13. Pubmed ID: 31353227; DOI: 10.1016/j.stemcr.2019.06.004; PMC: PMC6700605 MHHi001-AMHHi006-ASTBCi026-BMHHi007-AMHHi007-A-1 2019-08-13 2019-08-13 PubMed: 31353227 DOI: 10.1016/j.stemcr.2019.06.004Associated cell lines:
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Bilz NC, Willscher E, Binder H, Böhnke J, Stanifer ML, Hübner D, Boulant S, Liebert UG, Claus C
Teratogenic Rubella Virus Alters the Endodermal Differentiation Capacity of Human Induced Pluripotent Stem Cells
Bilz NC et al. Teratogenic Rubella Virus Alters the Endodermal Differentiation Capacity of Human Induced Pluripotent Stem Cells. . 2019-08-10. Pubmed ID: 31405163; DOI: 10.3390/cells8080870; PMC: PMC6721684 TMOi001-A 2019-08-10 2019-08-10 PubMed: 31405163 DOI: 10.3390/cells8080870Associated cell lines:
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de la Roche J, Angsutararux P, Kempf H, Janan M, Bolesani E, Thiemann S, Wojciechowski D, Coffee M, Franke A, Schwanke K, Leffler A, Luanpitpong S, Issaragrisil S, Fischer M, Zweigerdt R
Comparing human iPSC-cardiomyocytes versus HEK293T cells unveils disease-causing effects of Brugada mutation A735V of Na(V)1.5 sodium channels
de la Roche J et al. Comparing human iPSC-cardiomyocytes versus HEK293T cells unveils disease-causing effects of Brugada mutation A735V of Na(V)1.5 sodium channels. . 2019-08-01. Pubmed ID: 31371804; DOI: 10.1038/s41598-019-47632-4; PMC: PMC6673693 MUSIi009-A 2019-08-01 2019-08-01 PubMed: 31371804 DOI: 10.1038/s41598-019-47632-4Associated cell lines:
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Gatinois V, Desprat R, Becker F, Pichard L, Bernex F, Corsini C, Pellestor F, Lemaitre JM
Reprogramming of Human Peripheral Blood Mononuclear Cell (PBMC) from a patient suffering of a Werner syndrome resulting in iPSC line (REGUi003-A) maintaining a short telomere length
Gatinois V et al. Reprogramming of Human Peripheral Blood Mononuclear Cell (PBMC) from a patient suffering of a Werner syndrome resulting in iPSC line (REGUi003-A) maintaining a short telomere length. . 2019-08-00. Pubmed ID: 31404747; DOI: 10.1016/j.scr.2019.101515 REGUi003-A 2019-08-00 2019-08-00 PubMed: 31404747 DOI: 10.1016/j.scr.2019.101515Associated cell lines:
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van der Graaf LM, Gardiner SL, Tok M, Brands T, Boogaard MW, Pepers BA, Eussen B, de Klein A, Aziz NA, Freund C, Buijsen RAM, van Roon-Mom WMC
Generation of 5 induced pluripotent stem cell lines, LUMCi007-A and B and LUMCi008-A, B and C, from 2 patients with Huntington disease
van der Graaf LM et al. Generation of 5 induced pluripotent stem cell lines, LUMCi007-A and B and LUMCi008-A, B and C, from 2 patients with Huntington disease. . 2019-08-00. Pubmed ID: 31326748; DOI: 10.1016/j.scr.2019.101498 LUMCi002-ALUMCi003-ALUMCi007-ALUMCi007-BLUMCi008-ALUMCi008-BLUMCi008-C 2019-08-00 2019-08-00 PubMed: 31326748 DOI: 10.1016/j.scr.2019.101498Associated cell lines:
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Moore LR, Keller L, Bushart DD, Delatorre RG, Li D, McLoughlin HS, do Carmo Costa M, Shakkottai VG, Smith GD, Paulson HL
Antisense oligonucleotide therapy rescues aggresome formation in a novel spinocerebellar ataxia type 3 human embryonic stem cell line
Moore LR et al. Antisense oligonucleotide therapy rescues aggresome formation in a novel spinocerebellar ataxia type 3 human embryonic stem cell line. . 2019-08-00. Pubmed ID: 31374463; DOI: 10.1016/j.scr.2019.101504; PMC: PMC6736695 ZZUi004-AMUSIi004-AHIHCNi002-AUMICHe001-A 2019-08-00 2019-08-00 PubMed: 31374463 DOI: 10.1016/j.scr.2019.101504Associated cell lines:
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Kane MS, Zhao J, Muskett J, Diplock A, Srivastava S, Hauser N, Deeken JF, Niederhuber JE, Smith WE, Vilboux T, Ebrahimi-Fakhari D
EPG5 Variants with Modest Functional Impact Result in an Ameliorated and Primarily Neurological Phenotype in a 3.5-Year-Old Patient with Vici Syndrome
Kane MS et al. EPG5 Variants with Modest Functional Impact Result in an Ameliorated and Primarily Neurological Phenotype in a 3.5-Year-Old Patient with Vici Syndrome. . 2019-08-00. Pubmed ID: 31226715; DOI: 10.1055/s-0039-1692129 CIMRi001-A 2019-08-00 2019-08-00 PubMed: 31226715 DOI: 10.1055/s-0039-1692129Associated cell lines:
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Bhargava N, Jaitly S, Goswami SG, Jain S, Chakraborty D, Ramalingam S
Generation and characterization of induced pluripotent stem cell line (IGIBi001-A) from a sickle cell anemia patient with homozygous β-globin mutation
Bhargava N et al. Generation and characterization of induced pluripotent stem cell line (IGIBi001-A) from a sickle cell anemia patient with homozygous β-globin mutation. . 2019-08-00. Pubmed ID: 31255831; DOI: 10.1016/j.scr.2019.101484 IGIBi001-AIGIBi002-AIGIBi003-AIGIBi004-A 2019-08-00 2019-08-00 PubMed: 31255831 DOI: 10.1016/j.scr.2019.101484Associated cell lines:
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López-Márquez A, Alonso-Barroso E, Cerro-Tello G, Bravo-Alonso I, Arribas-Carreira L, Briso-Montiano Á, Navarrete R, Pérez-Cerdá C, Ugarte M, Pérez B, Desviat LR, Richard E
Corrigendum to "Generation and characterization of a human iPSC line (UAMi004-A) from a patient with propionic acidemia due to defects in the PCCB gene" [Stem Cell Research, Volume 38, July 2019, 101469]
López-Márquez A et al. Corrigendum to "Generation and characterization of a human iPSC line (UAMi004-A) from a patient with propionic acidemia due to defects in the PCCB gene" [Stem Cell Research, Volume 38, July 2019, 101469]. . 2019-08-00. Pubmed ID: 31365893; DOI: 10.1016/j.scr.2019.101513 UAMi004-A 2019-08-00 2019-08-00 PubMed: 31365893 DOI: 10.1016/j.scr.2019.101513Associated cell lines:
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Arribas-Carreira L, Bravo-Alonso I, López-Márquez A, Alonso-Barroso E, Briso-Montiano Á, Arroyo I, Ugarte M, Pérez B, Pérez-Cerdá C, Rodríguez-Pombo P, Richard E
Generation and characterization of a human iPSC line (UAMi005-A) from a patient with nonketotic hyperglycinemia due to mutations in the GLDC gene
Arribas-Carreira L et al. Generation and characterization of a human iPSC line (UAMi005-A) from a patient with nonketotic hyperglycinemia due to mutations in the GLDC gene. . 2019-08-00. Pubmed ID: 31349202; DOI: 10.1016/j.scr.2019.101503 UAMi005-A 2019-08-00 2019-08-00 PubMed: 31349202 DOI: 10.1016/j.scr.2019.101503Associated cell lines:
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Wang X, Malinowski AR, Beckenbauer J, Siehler J, Blöchinger A, Meitinger T, Häring HU, Staiger H, Burtscher I, Lickert H
Generation of a human induced pluripotent stem cell line (HMGUi002-A) from a healthy male individual
Wang X et al. Generation of a human induced pluripotent stem cell line (HMGUi002-A) from a healthy male individual. . 2019-08-00. Pubmed ID: 31419739; DOI: 10.1016/j.scr.2019.101531 HMGUi002-A 2019-08-00 2019-08-00 PubMed: 31419739 DOI: 10.1016/j.scr.2019.101531Associated cell lines:
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Park S, Yoo JE, Lee DR, Jang J, Cho MS, Kim DS, Kim DW
Establishment of PITX3-mCherry knock-in reporter human embryonic stem cell line (WAe009-A-23)
Park S et al. Establishment of PITX3-mCherry knock-in reporter human embryonic stem cell line (WAe009-A-23). . 2019-08-00. Pubmed ID: 31352199; DOI: 10.1016/j.scr.2019.101499 WAe009-AWAe009-A-23 2019-08-00 2019-08-00 PubMed: 31352199 DOI: 10.1016/j.scr.2019.101499Associated cell lines:
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Overeem AW, Klappe K, Parisi S, Klöters-Planchy P, Mataković L, du Teil Espina M, Drouin CA, Weiss KH, van IJzendoorn SCD
Pluripotent stem cell-derived bile canaliculi-forming hepatocytes to study genetic liver diseases involving hepatocyte polarity
Overeem AW et al. Pluripotent stem cell-derived bile canaliculi-forming hepatocytes to study genetic liver diseases involving hepatocyte polarity. . 2019-08-00. Pubmed ID: 30965071; DOI: 10.1016/j.jhep.2019.03.031 UMCGi010-A 2019-08-00 2019-08-00 PubMed: 30965071 DOI: 10.1016/j.jhep.2019.03.031Associated cell lines:
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Schuster J, Sobol M, Fatima A, Khalfallah A, Laan L, Anderlid BM, Nordgren A, Dahl N
Mowat-Wilson syndrome: Generation of two human iPS cell lines (UUIGPi004A and UUIGPi005A) from siblings with a truncating ZEB2 gene variant
Schuster J et al. Mowat-Wilson syndrome: Generation of two human iPS cell lines (UUIGPi004A and UUIGPi005A) from siblings with a truncating ZEB2 gene variant. . 2019-08-00. Pubmed ID: 31376723; DOI: 10.1016/j.scr.2019.101518 UUIGPi004-AUUIGPi005-A 2019-08-00 2019-08-00 PubMed: 31376723 DOI: 10.1016/j.scr.2019.101518Associated cell lines:
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Yang S, Cheng YS, Li R, Pradhan M, Hong J, Beers J, Zou J, Liu C, Might M, Rodems S, Zheng W
An induced pluripotent stem cell line (TRNDi010-C) from a patient carrying a homozygous p.R401X mutation in the NGLY1 gene
Yang S et al. An induced pluripotent stem cell line (TRNDi010-C) from a patient carrying a homozygous p.R401X mutation in the NGLY1 gene. . 2019-08-00. Pubmed ID: 31326749; DOI: 10.1016/j.scr.2019.101496; PMC: PMC6910241 TRNDi010-C 2019-08-00 2019-08-00 PubMed: 31326749 DOI: 10.1016/j.scr.2019.101496Associated cell lines:
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Giri S, Purushottam M, Viswanath B, Muddashetty RS
Generation of a FMR1 homozygous knockout human embryonic stem cell line (WAe009-A-16) by CRISPR/Cas9 editing
Giri S et al. Generation of a FMR1 homozygous knockout human embryonic stem cell line (WAe009-A-16) by CRISPR/Cas9 editing. . 2019-08-00. Pubmed ID: 31280136; DOI: 10.1016/j.scr.2019.101494 WAe001-AWAe009-AWAe001-A-20WAe009-A-16 2019-08-00 2019-08-00 PubMed: 31280136 DOI: 10.1016/j.scr.2019.101494Associated cell lines:
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Fernandes S, Vinnakota R, Kumar J, Kale V, Limaye L
Improved neural differentiation of normal and abnormal induced pluripotent stem cell lines in the presence of valproic acid
Fernandes S et al. Improved neural differentiation of normal and abnormal induced pluripotent stem cell lines in the presence of valproic acid. . 2019-08-00. Pubmed ID: 31148385; DOI: 10.1002/term.2904 NCCSi002-ANCCSi003-A 2019-08-00 2019-08-00 PubMed: 31148385 DOI: 10.1002/term.2904Associated cell lines:
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Kolundzic N, Khurana P, Devito L, Jeriha J, Marx J, Hobbs C, Wong XFCC, Common JEA, Liovic M, Dubrac S, Gruber R, Schmuth M, Mauro TM, Ilic D
Induced pluripotent stem cell line heterozygous for p.R501X mutation in filaggrin: KCLi003-A
Kolundzic N et al. Induced pluripotent stem cell line heterozygous for p.R501X mutation in filaggrin: KCLi003-A. . 2019-08-00. Pubmed ID: 31408836; DOI: 10.1016/j.scr.2019.101527 KCLi003-A 2019-08-00 2019-08-00 PubMed: 31408836 DOI: 10.1016/j.scr.2019.101527Associated cell lines:
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Mura M, Pisano F, Stefanello M, Ginevrino M, Boni M, Calabrò F, Crotti L, Valente EM, Schwartz PJ, Brink PA, Gnecchi M
Generation of two human induced pluripotent stem cell (hiPSC) lines from a long QT syndrome South African founder population
Mura M et al. Generation of two human induced pluripotent stem cell (hiPSC) lines from a long QT syndrome South African founder population. . 2019-08-00. Pubmed ID: 31398660; DOI: 10.1016/j.scr.2019.101510 PSMi001-APSMi008-A 2019-08-00 2019-08-00 PubMed: 31398660 DOI: 10.1016/j.scr.2019.101510 -
Yamamoto T, Otsu M, Okumura T, Horie Y, Ueno Y, Taniguchi H, Ohtaka M, Nakanishi M, Abe Y, Murase T, Umehara T, Ikematsu K
Generation of three induced pluripotent stem cell lines from postmortem tissue derived following sudden death of a young patient with STXBP1 mutation
Yamamoto T et al. Generation of three induced pluripotent stem cell lines from postmortem tissue derived following sudden death of a young patient with STXBP1 mutation. . 2019-08-00. Pubmed ID: 31255830; DOI: 10.1016/j.scr.2019.101485 IMSUTi001-AIMSUTi001-BIMSUTi001-C 2019-08-00 2019-08-00 PubMed: 31255830 DOI: 10.1016/j.scr.2019.101485Associated cell lines:
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Bai X, Yang XJ, Chen L
Generation of an integration-free induced pluripotent stem cell line (FDEENTi003-A) from a patient with pathological myopia
Bai X et al. Generation of an integration-free induced pluripotent stem cell line (FDEENTi003-A) from a patient with pathological myopia. . 2019-08-00. Pubmed ID: 31376721; DOI: 10.1016/j.scr.2019.101495; PMC: PMC7077977 FDEENTi003-A 2019-08-00 2019-08-00 PubMed: 31376721 DOI: 10.1016/j.scr.2019.101495Associated cell lines:
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Zhang H, Ma Y, Song F, Yang X, Li Y, Guan J, Lv Y, Gao M, Ma J, Liu Y, Gai Z
Generation of an induced pluripotent stem cell line (SDQLCHi003-a) from a patient with short rib-thoracic dysplasia syndrome type III carrying compound heterozygous mutations in DYNC2H1
Zhang H et al. Generation of an induced pluripotent stem cell line (SDQLCHi003-a) from a patient with short rib-thoracic dysplasia syndrome type III carrying compound heterozygous mutations in DYNC2H1. . 2019-08-00. Pubmed ID: 31415973; DOI: 10.1016/j.scr.2019.101505 SDQLCHi003-A 2019-08-00 2019-08-00 PubMed: 31415973 DOI: 10.1016/j.scr.2019.101505Associated cell lines:
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Netsrithong R, Promnakhon N, Boonkaew B, Vatanashevanopakorn C, Pattanapanyasat K, Wattanapanitch M
Generation of two induced pluripotent stem cell lines (MUSIi011-A and MUSIi011-B) from peripheral blood T lymphocytes of a healthy individual
Netsrithong R et al. Generation of two induced pluripotent stem cell lines (MUSIi011-A and MUSIi011-B) from peripheral blood T lymphocytes of a healthy individual. . 2019-08-00. Pubmed ID: 31229899; DOI: 10.1016/j.scr.2019.101487 MUSIi011-AMUSIi011-B 2019-08-00 2019-08-00 PubMed: 31229899 DOI: 10.1016/j.scr.2019.101487Associated cell lines:
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Bozaoglu K, Gao Y, Stanley E, Fanjul-Fernández M, Brown NJ, Pope K, Green CC, Vlahos K, Sourris K, Bahlo M, Delatycki M, Scheffer I, Lockhart PJ
Generation of seven iPSC lines from peripheral blood mononuclear cells suitable to investigate Autism Spectrum Disorder
Bozaoglu K et al. Generation of seven iPSC lines from peripheral blood mononuclear cells suitable to investigate Autism Spectrum Disorder. . 2019-08-00. Pubmed ID: 31415975; DOI: 10.1016/j.scr.2019.101516 MCRIi011-AMCRIi012-AMCRIi013-AMCRIi014-AMCRIi015-AMCRIi016-AMCRIi017-A 2019-08-00 2019-08-00 PubMed: 31415975 DOI: 10.1016/j.scr.2019.101516Associated cell lines:
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Tang C, Lu C, Ji X, Ma L, Zhou Q, Xiong M, Zhou W
Generation of two induced pluripotent stem cell (iPSC) lines from human breast milk using episomal reprogramming system
Tang C et al. Generation of two induced pluripotent stem cell (iPSC) lines from human breast milk using episomal reprogramming system. . 2019-08-00. Pubmed ID: 31404746; DOI: 10.1016/j.scr.2019.101511 FDCHi001-AFDCHi002-A 2019-08-00 2019-08-00 PubMed: 31404746 DOI: 10.1016/j.scr.2019.101511Associated cell lines:
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Tongkobpetch S, Rungsiwiwut R, Pruksananonda K, Suphapeetiporn K, Shotelersuk V
Generation of two human iPSC lines (MDCUi001-A and MDCUi001-B) from dermal fibroblasts of a Thai patient with X-linked osteogenesis imperfecta using integration-free Sendai virus
Tongkobpetch S et al. Generation of two human iPSC lines (MDCUi001-A and MDCUi001-B) from dermal fibroblasts of a Thai patient with X-linked osteogenesis imperfecta using integration-free Sendai virus. . 2019-08-00. Pubmed ID: 31326747; DOI: 10.1016/j.scr.2019.101493 MDCUi001-AMDCUi001-B 2019-08-00 2019-08-00 PubMed: 31326747 DOI: 10.1016/j.scr.2019.101493Associated cell lines:
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Olmer R, Dahlmann J, Merkert S, Baus S, Göhring G, Martin U
Generation of a NKX2.1 knock-in reporter cell line from human induced pluripotent stem cells (MHHi006-A-2)
Olmer R et al. Generation of a NKX2.1 knock-in reporter cell line from human induced pluripotent stem cells (MHHi006-A-2). . 2019-08-00. Pubmed ID: 31299562; DOI: 10.1016/j.scr.2019.101492 MHHi006-AMHHi006-A-2 2019-08-00 2019-08-00 PubMed: 31299562 DOI: 10.1016/j.scr.2019.101492Associated cell lines:
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Khan M, Zende S, Vaidyanath A, Avatade R, Shiras A
Generation of two induced pluripotent stem cell lines NCCSi005A and NCCSi006A from CD4(+)T cells of healthy individuals of Indian origin
Khan M et al. Generation of two induced pluripotent stem cell lines NCCSi005A and NCCSi006A from CD4(+)T cells of healthy individuals of Indian origin. . 2019-08-00. Pubmed ID: 31352200; DOI: 10.1016/j.scr.2019.101506 NCCSi005-ANCCSi006-ANCCSi005-BNCCSi005-CNCCSi006-BNCCSi006-C 2019-08-00 2019-08-00 PubMed: 31352200 DOI: 10.1016/j.scr.2019.101506Associated cell lines:
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Díaz-Guerra E, Moreno-Jiménez EP, de Rojas I, Rodríguez C, Rodríguez-Traver E, Arribas-González E, Orera M, Hernández I, Ruiz A, Vicario C
A collection of four integration-free iPSC lines derived from diagnosed sporadic Alzheimer's disease patients with different APOE alleles
Díaz-Guerra E et al. A collection of four integration-free iPSC lines derived from diagnosed sporadic Alzheimer's disease patients with different APOE alleles. . 2019-08-00. Pubmed ID: 31401456; DOI: 10.1016/j.scr.2019.101522 ICCSICi008-AICCSICi009-AICCSICi010-AICCSICi011-A 2019-08-00 2019-08-00 PubMed: 31401456 DOI: 10.1016/j.scr.2019.101522Associated cell lines:
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Zhang Y, Li A, Huang CL, Wang G, Wang D
Generation of induced pluripotent stem cells (iPSCs) from an infant with catecholaminergic polymorphic ventricular tachycardia carrying the double heterozygous mutations A1855D in RyR2 and Q1362H in SCN10A
Zhang Y et al. Generation of induced pluripotent stem cells (iPSCs) from an infant with catecholaminergic polymorphic ventricular tachycardia carrying the double heterozygous mutations A1855D in RyR2 and Q1362H in SCN10A. . 2019-08-00. Pubmed ID: 31382203; DOI: 10.1016/j.scr.2019.101509 XACHi001-A 2019-08-00 2019-08-00 PubMed: 31382203 DOI: 10.1016/j.scr.2019.101509Associated cell lines:
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Li C, Wang Q, Peng Z, Lin Y, Liu H, Yang X, Li S, Liu X, Chen J
Generation of FOS gene knockout lines from a human embryonic stem cell line using CRISPR/Cas9
Li C et al. Generation of FOS gene knockout lines from a human embryonic stem cell line using CRISPR/Cas9. . 2019-08-00. Pubmed ID: 31229900; DOI: 10.1016/j.scr.2019.101479 WAe001-A-23WAe001-A-24 2019-08-00 2019-08-00 PubMed: 31229900 DOI: 10.1016/j.scr.2019.101479Associated cell lines:
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Sampaio GLA, Martins GLS, Paredes BD, Nonaka CKV, da Silva KN, Rossi EA, Dos Santos RR, Soares MBP, Souza BSF
Generation of an induced pluripotent stem cell line from a patient with autism spectrum disorder and SCN2A haploinsufficiency
Sampaio GLA et al. Generation of an induced pluripotent stem cell line from a patient with autism spectrum disorder and SCN2A haploinsufficiency. . 2019-08-00. Pubmed ID: 31272037; DOI: 10.1016/j.scr.2019.101488 CBTCi008-A 2019-08-00 2019-08-00 PubMed: 31272037 DOI: 10.1016/j.scr.2019.101488Associated cell lines:
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Tofoli FA, Chien HF, Barbosa ER, Pereira LV
Generation of three human induced pluripotent stem cell (hiPSC) lines derived from one Gaucher disease patient with Parkinson's disease and two unrelated Parkinson's disease patients with GBA mutations
Tofoli FA et al. Generation of three human induced pluripotent stem cell (hiPSC) lines derived from one Gaucher disease patient with Parkinson's disease and two unrelated Parkinson's disease patients with GBA mutations. . 2019-08-00. Pubmed ID: 31401455; DOI: 10.1016/j.scr.2019.101519 LANCEi011-ALANCEi012-ALANCEi013-A 2019-08-00 2019-08-00 PubMed: 31401455 DOI: 10.1016/j.scr.2019.101519Associated cell lines:
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Kozlowska E, Ciolak A, Olejniczak M, Fiszer A
Generation of human iPS cell line IBCHi001-A from dentatorubral-pallidoluysian atrophy patient's fibroblasts
Kozlowska E et al. Generation of human iPS cell line IBCHi001-A from dentatorubral-pallidoluysian atrophy patient's fibroblasts. . 2019-08-00. Pubmed ID: 31374462; DOI: 10.1016/j.scr.2019.101512 IBCHi001-A 2019-08-00 2019-08-00 PubMed: 31374462 DOI: 10.1016/j.scr.2019.101512Associated cell lines:
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Menges J, Cremanns M, Steenpass L
Generation of two H1 hESC sublines carrying deletions of RB1 exon 1/promoter in heterozygous or compound heterozygous state
Menges J et al. Generation of two H1 hESC sublines carrying deletions of RB1 exon 1/promoter in heterozygous or compound heterozygous state. . 2019-08-00. Pubmed ID: 31404748; DOI: 10.1016/j.scr.2019.101517 WAe001-A-31WAe001-A-32 2019-08-00 2019-08-00 PubMed: 31404748 DOI: 10.1016/j.scr.2019.101517Associated cell lines:
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Ge N, Liu M, Krawczyk J, McInerney V, Galvin J, Shen S, O'Brien T, Prendiville T
Generation of eight human induced pluripotent stem cell (iPSC) lines from familial Long QT Syndrome type 1 (LQT1) patients carrying KCNQ1 c.1697C>A mutation (NUIGi005-A, NUIGi005-B, NUIGi005-C, NUIGi006-A, NUIGi006-B, NUIGi006-C, NUIGi007-A, and NUIGi007-B)
Ge N et al. Generation of eight human induced pluripotent stem cell (iPSC) lines from familial Long QT Syndrome type 1 (LQT1) patients carrying KCNQ1 c.1697C>A mutation (NUIGi005-A, NUIGi005-B, NUIGi005-C, NUIGi006-A, NUIGi006-B, NUIGi006-C, NUIGi007-A, and NUIGi007-B). . 2019-08-00. Pubmed ID: 31415974; DOI: 10.1016/j.scr.2019.101502 NUIGi005-ANUIGi005-BNUIGi005-CNUIGi006-ANUIGi006-BNUIGi006-CNUIGi007-ANUIGi007-B 2019-08-00 2019-08-00 PubMed: 31415974 DOI: 10.1016/j.scr.2019.101502Associated cell lines:
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Domozhirov AY, Mazzilli JL, Wetsel RA, Zsigmond EM
Generation of CDMLe012-A-1 cells: A pluripotent human embryonic stem cell model of Turner's syndrome
Domozhirov AY et al. Generation of CDMLe012-A-1 cells: A pluripotent human embryonic stem cell model of Turner's syndrome. . 2019-08-00. Pubmed ID: 31357114; DOI: 10.1016/j.scr.2019.101508 CDMLe012-ACDMLe012-A-1 2019-08-00 2019-08-00 PubMed: 31357114 DOI: 10.1016/j.scr.2019.101508Associated cell lines:
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Gubert F, Vasques JF, Cozendey TD, Domizi P, Toledo MF, Kasai-Brunswick TH, Hochman-Mendez C, Junior MC, Zembrzuski VM, Loureiro MPS, Lima JMB, Gress CH, Cabello GMK, Cabello PH, Borgonovo T, Vaz IM, Silva R, Mendez-Otero R
Generation of patient-specific pluripotent induced stem cell line UFRJi007-A from a Brazilian familial amyotrophic lateral sclerosis patient
Gubert F et al. Generation of patient-specific pluripotent induced stem cell line UFRJi007-A from a Brazilian familial amyotrophic lateral sclerosis patient. . 2019-08-00. Pubmed ID: 31301488; DOI: 10.1016/j.scr.2019.101490 UFRJi007-A 2019-08-00 2019-08-00 PubMed: 31301488 DOI: 10.1016/j.scr.2019.101490Associated cell lines:
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Schuster J, Fatima A, Sobol M, Norradin FH, Laan L, Dahl N
Generation of three human induced pluripotent stem cell (iPSC) lines from three patients with Dravet syndrome carrying distinct SCN1A gene mutations
Schuster J et al. Generation of three human induced pluripotent stem cell (iPSC) lines from three patients with Dravet syndrome carrying distinct SCN1A gene mutations. . 2019-08-00. Pubmed ID: 31400703; DOI: 10.1016/j.scr.2019.101523 UUIGPi006-AUUIGPi007-AUUIGPi008-A 2019-08-00 2019-08-00 PubMed: 31400703 DOI: 10.1016/j.scr.2019.101523Associated cell lines:
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Kulcenty K, Wroblewska JP, Rucinski M, Kozlowska E, Jopek K, Suchorska WM
MicroRNA Profiling During Neural Differentiation of Induced Pluripotent Stem Cells
Kulcenty K et al. MicroRNA Profiling During Neural Differentiation of Induced Pluripotent Stem Cells. . 2019-07-26. Pubmed ID: 31357387; DOI: 10.3390/ijms20153651; PMC: PMC6696086 GPCCi001-A 2019-07-26 2019-07-26 PubMed: 31357387 DOI: 10.3390/ijms20153651Associated cell lines:
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Regent F, Morizur L, Lesueur L, Habeler W, Plancheron A, Ben M'Barek K, Monville C
Automation of human pluripotent stem cell differentiation toward retinal pigment epithelial cells for large-scale productions
Regent F et al. Automation of human pluripotent stem cell differentiation toward retinal pigment epithelial cells for large-scale productions. . 2019-07-23. Pubmed ID: 31337830; DOI: 10.1038/s41598-019-47123-6; PMC: PMC6650487 RCe013-A 2019-07-23 2019-07-23 PubMed: 31337830 DOI: 10.1038/s41598-019-47123-6Associated cell lines:
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Okur FV, Cevher İ, Özdemir C, Kocaefe Ç, Çetinkaya DU
Osteopetrotic induced pluripotent stem cells derived from patients with different disease-associated mutations by non-integrating reprogramming methods
Okur FV et al. Osteopetrotic induced pluripotent stem cells derived from patients with different disease-associated mutations by non-integrating reprogramming methods. . 2019-07-17. Pubmed ID: 31315669; DOI: 10.1186/s13287-019-1316-8; PMC: PMC6637500 KSCBi003-A 2019-07-17 2019-07-17 PubMed: 31315669 DOI: 10.1186/s13287-019-1316-8Associated cell lines:
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Skarnes WC, Pellegrino E, McDonough JA
Improving homology-directed repair efficiency in human stem cells
Skarnes WC et al. Improving homology-directed repair efficiency in human stem cells. . 2019-07-15. Pubmed ID: 31216442; DOI: 10.1016/j.ymeth.2019.06.016 WTSIi018-BWTSIi018-B-1 2019-07-15 2019-07-15 PubMed: 31216442 DOI: 10.1016/j.ymeth.2019.06.016Associated cell lines:
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Zhang XH, Šarić T, Mehrjardi NZ, Hamad S, Morad M
Acid-Sensitive Ion Channels Are Expressed in Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes
Zhang XH et al. Acid-Sensitive Ion Channels Are Expressed in Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes. . 2019-07-15. Pubmed ID: 31119982; DOI: 10.1089/scd.2018.0234; PMC: PMC6648204 UKKi011-A 2019-07-15 2019-07-15 PubMed: 31119982 DOI: 10.1089/scd.2018.0234Associated cell lines:
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Jiang C, Zeng X, Xue B, Campbell D, Wang Y, Sun H, Xu Y, Wen X
Screening of pure synthetic coating substrates for induced pluripotent stem cells and iPSC-derived neuroepithelial progenitors with short peptide based integrin array
Jiang C et al. Screening of pure synthetic coating substrates for induced pluripotent stem cells and iPSC-derived neuroepithelial progenitors with short peptide based integrin array. . 2019-07-01. Pubmed ID: 30981669; DOI: 10.1016/j.yexcr.2019.04.013 ZZUi011-A 2019-07-01 2019-07-01 PubMed: 30981669 DOI: 10.1016/j.yexcr.2019.04.013Associated cell lines:
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Bolinches-Amorós A, León M, Del Buey Furió V, Marfany G, Gonzàlez-Duarte R, Erceg S, Lukovic D
Generation of an iPSC line from a retinitis pigmentosa patient carrying a homozygous mutation in CERKL and a healthy sibling
Bolinches-Amorós A et al. Generation of an iPSC line from a retinitis pigmentosa patient carrying a homozygous mutation in CERKL and a healthy sibling. . 2019-07-00. Pubmed ID: 31082679; DOI: 10.1016/j.scr.2019.101455 ESi066-AESi067-A 2019-07-00 2019-07-00 PubMed: 31082679 DOI: 10.1016/j.scr.2019.101455 -
Paredes BD, Martins GLS, Azevedo CM, Sampaio GLA, Nonaka CKV, Silva KND, Soares MBP, Santos RRD, Souza BSF
Generation of three control iPS cell lines for sickle cell disease studies by reprogramming erythroblasts from individuals without hemoglobinopathies
Paredes BD et al. Generation of three control iPS cell lines for sickle cell disease studies by reprogramming erythroblasts from individuals without hemoglobinopathies. . 2019-07-00. Pubmed ID: 31078962; DOI: 10.1016/j.scr.2019.101454 CBTCi002-ACBTCi003-ACBTCi004-A 2019-07-00 2019-07-00 PubMed: 31078962 DOI: 10.1016/j.scr.2019.101454Associated cell lines:
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Howden S, Hosseini Far H, Motazedian A, Elefanty AG, Stanley EG, Lamandé SR, Bateman JF
The use of simultaneous reprogramming and gene correction to generate an osteogenesis imperfecta patient COL1A1 c. 3936 G>T iPSC line and an isogenic control iPSC line
Howden S et al. The use of simultaneous reprogramming and gene correction to generate an osteogenesis imperfecta patient COL1A1 c. 3936 G>T iPSC line and an isogenic control iPSC line. . 2019-07-00. Pubmed ID: 31082677; DOI: 10.1016/j.scr.2019.101453 MCRIi018-AMCRIi018-B 2019-07-00 2019-07-00 PubMed: 31082677 DOI: 10.1016/j.scr.2019.101453Associated cell lines:
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Kolundzic N, Khurana P, Devito L, Donne M, Hobbs C, Jeriha J, Wong XFCC, Common JAE, Lane EB, Dubrac S, Gruber R, Schmuth M, Mauro TM, Ilic D
Induced pluripotent stem cell line heterozygous for p.R2447X mutation in filaggrin: KCLi002-A
Kolundzic N et al. Induced pluripotent stem cell line heterozygous for p.R2447X mutation in filaggrin: KCLi002-A. . 2019-07-00. Pubmed ID: 31103941; DOI: 10.1016/j.scr.2019.101462 KCLi002-A 2019-07-00 2019-07-00 PubMed: 31103941 DOI: 10.1016/j.scr.2019.101462Associated cell lines:
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Greuel S, Hanci G, Böhme M, Miki T, Schubert F, Sittinger M, Mandenius CF, Zeilinger K, Freyer N
Effect of inoculum density on human-induced pluripotent stem cell expansion in 3D bioreactors
Greuel S et al. Effect of inoculum density on human-induced pluripotent stem cell expansion in 3D bioreactors. . 2019-07-00. Pubmed ID: 31069891; DOI: 10.1111/cpr.12604; PMC: PMC6668975 ZZUi009-A 2019-07-00 2019-07-00 PubMed: 31069891 DOI: 10.1111/cpr.12604Associated cell lines:
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López-Márquez A, Alonso-Barroso E, Cerro-Tello G, Bravo-Alonso I, Arribas-Carreira L, Briso-Montiano Á, Navarrete R, Pérez-Cerdá C, Ugarte M, Pérez B, Desviat LR, Richard E
Generation and characterization of a human iPSC line (UAMi004-A) from a patient with propionic acidemia due to defects in the PCCB gene
López-Márquez A et al. Generation and characterization of a human iPSC line (UAMi004-A) from a patient with propionic acidemia due to defects in the PCCB gene. . 2019-07-00. Pubmed ID: 31132581; DOI: 10.1016/j.scr.2019.101469 UAMi004-A 2019-07-00 2019-07-00 PubMed: 31132581 DOI: 10.1016/j.scr.2019.101469Associated cell lines:
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Yan X, Guo Y, Chen J, Cui Z, Gu J, Wang Y, Mao S, Ding C, Chen J, Tang S
Establishment of CSUASOi001-A, a non-integrated induced pluripotent stem cell line from urine-derived cells of a Chinese patient carrying RS1 gene mutation
Yan X et al. Establishment of CSUASOi001-A, a non-integrated induced pluripotent stem cell line from urine-derived cells of a Chinese patient carrying RS1 gene mutation. . 2019-07-00. Pubmed ID: 31141763; DOI: 10.1016/j.scr.2019.101466 CSUASOi001-A 2019-07-00 2019-07-00 PubMed: 31141763 DOI: 10.1016/j.scr.2019.101466Associated cell lines:
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Domingo-Prim J, Riera M, Burés-Jelstrup A, Corcostegui B, Pomares E
Establishment of an induced pluripotent stem cell line (FRIMOi005-A) derived from a retinitis pigmentosa patient carrying a dominant mutation in RHO gene
Domingo-Prim J et al. Establishment of an induced pluripotent stem cell line (FRIMOi005-A) derived from a retinitis pigmentosa patient carrying a dominant mutation in RHO gene. . 2019-07-00. Pubmed ID: 31146251; DOI: 10.1016/j.scr.2019.101468 FRIMOi005-A 2019-07-00 2019-07-00 PubMed: 31146251 DOI: 10.1016/j.scr.2019.101468Associated cell lines:
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Chen G, Jin H, Yu Z, Liu Y, Li Z, Navarengom K, Schwartzbeck R, Dmitrieva N, Cudrici C, Ferrante EA, Biesecker LG, Yang D, Boehm M
Generation of human induced pluripotent stem cells from individuals with a homozygous CCR5Δ32 mutation
Chen G et al. Generation of human induced pluripotent stem cells from individuals with a homozygous CCR5Δ32 mutation. . 2019-07-00. Pubmed ID: 31234109; DOI: 10.1016/j.scr.2019.101481; PMC: PMC6662727 NIHTVBi001-ANIHTVBi002-ANIHTVBi003-A 2019-07-00 2019-07-00 PubMed: 31234109 DOI: 10.1016/j.scr.2019.101481Associated cell lines:
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Üçeyler N, Urlaub D, Mayer C, Uehlein S, Held M, Sommer C
Tumor necrosis factor-α links heat and inflammation with Fabry pain
Üçeyler N et al. Tumor necrosis factor-α links heat and inflammation with Fabry pain. . 2019-07-00. Pubmed ID: 31221509; DOI: 10.1016/j.ymgme.2019.05.009 UKWNLi001-A 2019-07-00 2019-07-00 PubMed: 31221509 DOI: 10.1016/j.ymgme.2019.05.009Associated cell lines:
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Garcia-Delgado AB, Calado SM, Valdes-Sanchez LM, Montero-Sanchez A, Ponte-Zuñiga B, de la Cerda B, Bhattacharya SS, Diaz-Corrales FJ
Generation of a human iPS cell line (CABi003-A) from a patient with age-related macular degeneration carrying the CFH Y402H polymorphism
Garcia-Delgado AB et al. Generation of a human iPS cell line (CABi003-A) from a patient with age-related macular degeneration carrying the CFH Y402H polymorphism. . 2019-07-00. Pubmed ID: 31176916; DOI: 10.1016/j.scr.2019.101473 CABi003-A 2019-07-00 2019-07-00 PubMed: 31176916 DOI: 10.1016/j.scr.2019.101473Associated cell lines:
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Sun J, Zhang X, Cong Q, Wang C, Chen D, Wang Y, Wang X, Yi Z, Qin S
Generation of refractory schizophrenia patient-derived induced pluripotent stem cell line UJSi001-A
Sun J et al. Generation of refractory schizophrenia patient-derived induced pluripotent stem cell line UJSi001-A. . 2019-07-00. Pubmed ID: 31102833; DOI: 10.1016/j.scr.2019.101460 UJSi001-A 2019-07-00 2019-07-00 PubMed: 31102833 DOI: 10.1016/j.scr.2019.101460Associated cell lines:
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Altieri F, D'Anzi A, Martello F, Tardivo S, Spasari I, Ferrari D, Bernardini L, Lamorte G, Mazzoccoli G, Valente EM, Vescovi AL, Rosati J
Production and characterization of human induced pluripotent stem cells (iPSC) CSSi007-A (4383) from Joubert Syndrome
Altieri F et al. Production and characterization of human induced pluripotent stem cells (iPSC) CSSi007-A (4383) from Joubert Syndrome. . 2019-07-00. Pubmed ID: 31202121; DOI: 10.1016/j.scr.2019.101480; PMC: PMC6617992 CSSi007-A 2019-07-00 2019-07-00 PubMed: 31202121 DOI: 10.1016/j.scr.2019.101480Associated cell lines:
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Schuster J, Fatima A, Schwarz F, Klar J, Laan L, Dahl N
Generation of human induced pluripotent stem cell (iPSC) lines from three patients with von Hippel-Lindau syndrome carrying distinct VHL gene mutations
Schuster J et al. Generation of human induced pluripotent stem cell (iPSC) lines from three patients with von Hippel-Lindau syndrome carrying distinct VHL gene mutations. . 2019-07-00. Pubmed ID: 31176917; DOI: 10.1016/j.scr.2019.101474 UUIGPi001-AUUIGPi002-AUUIGPi003-A 2019-07-00 2019-07-00 PubMed: 31176917 DOI: 10.1016/j.scr.2019.101474Associated cell lines:
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Bai X, Yang XJ, Chen L
Establishment of an induced pluripotent stem cell line (FDEENTi002-A) from a patient with Best's disease carrying c.888C > A mutation in BEST1 gene
Bai X et al. Establishment of an induced pluripotent stem cell line (FDEENTi002-A) from a patient with Best's disease carrying c.888C > A mutation in BEST1 gene. . 2019-07-00. Pubmed ID: 31146250; DOI: 10.1016/j.scr.2019.101459; PMC: PMC7156156 FDEENTi002-A 2019-07-00 2019-07-00 PubMed: 31146250 DOI: 10.1016/j.scr.2019.101459Associated cell lines:
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Tantarungsee N, Bostan Ali Z, Soi-Ampornkul R, Rujitharanawong C, Subchookul C, Ritthaphai A, Boonkaew B, Wattanapanitch M, Thanomkitti K, Triwongwaranat D, Vatanashevanopakorn C, Thuangtong R
Generation of an integration-free human induced pluripotent stem cell line MUSIi010-A from occipital scalp fibroblasts of a male patient with androgenetic alopecia
Tantarungsee N et al. Generation of an integration-free human induced pluripotent stem cell line MUSIi010-A from occipital scalp fibroblasts of a male patient with androgenetic alopecia. . 2019-07-00. Pubmed ID: 31228683; DOI: 10.1016/j.scr.2019.101486 MUSIi010-A 2019-07-00 2019-07-00 PubMed: 31228683 DOI: 10.1016/j.scr.2019.101486Associated cell lines:
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Rodríguez-Traver E, Díaz-Guerra E, Rodríguez C, Fernández P, Arenas F, Araúzo-Bravo M, Orera M, Kulisevsky J, Moratalla R, Vicario C
A collection of integration-free iPSCs derived from Parkinson's disease patients carrying mutations in the GBA1 gene
Rodríguez-Traver E et al. A collection of integration-free iPSCs derived from Parkinson's disease patients carrying mutations in the GBA1 gene. . 2019-07-00. Pubmed ID: 31203165; DOI: 10.1016/j.scr.2019.101482 ICCSICi001-AICCSICi002-AICCSICi003-AICCSICi004-A 2019-07-00 2019-07-00 PubMed: 31203165 DOI: 10.1016/j.scr.2019.101482Associated cell lines:
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Erkilic N, Sanjurjo-Soriano C, Manes G, Dubois G, Hamel CP, Meunier I, Kalatzis V
Generation of a human iPSC line, INMi004-A, with a point mutation in CRX associated with autosomal dominant Leber congenital amaurosis
Erkilic N et al. Generation of a human iPSC line, INMi004-A, with a point mutation in CRX associated with autosomal dominant Leber congenital amaurosis. . 2019-07-00. Pubmed ID: 31247521; DOI: 10.1016/j.scr.2019.101476 INMi004-A 2019-07-00 2019-07-00 PubMed: 31247521 DOI: 10.1016/j.scr.2019.101476Associated cell lines:
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Baskfield A, Li R, Beers J, Zou J, Liu C, Zheng W
An induced pluripotent stem cell line (TRNDi009-C) from a Niemann-Pick disease type A patient carrying a heterozygous p.L302P (c.905 T>C) mutation in the SMPD1 gene
Baskfield A et al. An induced pluripotent stem cell line (TRNDi009-C) from a Niemann-Pick disease type A patient carrying a heterozygous p.L302P (c.905 T>C) mutation in the SMPD1 gene. . 2019-07-00. Pubmed ID: 31132580; DOI: 10.1016/j.scr.2019.101461; PMC: PMC6686851 TRNDi009-C 2019-07-00 2019-07-00 PubMed: 31132580 DOI: 10.1016/j.scr.2019.101461Associated cell lines:
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Erkilic N, Sanjurjo-Soriano C, Diakatou M, Manes G, Dubois G, Hamel CP, Meunier I, Kalatzis V
Generation of a human iPSC line, INMi003-A, with a missense mutation in CRX associated with autosomal dominant cone-rod dystrophy
Erkilic N et al. Generation of a human iPSC line, INMi003-A, with a missense mutation in CRX associated with autosomal dominant cone-rod dystrophy. . 2019-07-00. Pubmed ID: 31203166; DOI: 10.1016/j.scr.2019.101478 INMi003-A 2019-07-00 2019-07-00 PubMed: 31203166 DOI: 10.1016/j.scr.2019.101478Associated cell lines:
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Park CY, Sung JJ, Cho SR, Kim J, Kim DW
Universal Correction of Blood Coagulation Factor VIII in Patient-Derived Induced Pluripotent Stem Cells Using CRISPR/Cas9
Park CY et al. Universal Correction of Blood Coagulation Factor VIII in Patient-Derived Induced Pluripotent Stem Cells Using CRISPR/Cas9. . 2019-06-11. Pubmed ID: 31105049; DOI: 10.1016/j.stemcr.2019.04.016; PMC: PMC6565751 YCMi001-B 2019-06-11 2019-06-11 PubMed: 31105049 DOI: 10.1016/j.stemcr.2019.04.016Associated cell lines:
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Zhang J, McIntosh BE, Wang B, Brown ME, Probasco MD, Webster S, Duffin B, Zhou Y, Guo LW, Burlingham WJ, Kent C, Ferris M, Thomson JA
A Human Pluripotent Stem Cell-Based Screen for Smooth Muscle Cell Differentiation and Maturation Identifies Inhibitors of Intimal Hyperplasia
Zhang J et al. A Human Pluripotent Stem Cell-Based Screen for Smooth Muscle Cell Differentiation and Maturation Identifies Inhibitors of Intimal Hyperplasia. . 2019-06-11. Pubmed ID: 31080110; DOI: 10.1016/j.stemcr.2019.04.013; PMC: PMC6565755 WAe001-A-1X 2019-06-11 2019-06-11 PubMed: 31080110 DOI: 10.1016/j.stemcr.2019.04.013Associated cell lines:
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Merkert S, Schubert M, Olmer R, Engels L, Radetzki S, Veltman M, Scholte BJ, Zöllner J, Pedemonte N, Galietta LJV, von Kries JP, Martin U
High-Throughput Screening for Modulators of CFTR Activity Based on Genetically Engineered Cystic Fibrosis Disease-Specific iPSCs
Merkert S et al. High-Throughput Screening for Modulators of CFTR Activity Based on Genetically Engineered Cystic Fibrosis Disease-Specific iPSCs. . 2019-06-11. Pubmed ID: 31080112; DOI: 10.1016/j.stemcr.2019.04.014; PMC: PMC6565754 MHHi001-AMHHi002-AMHHi006-AMHHi006-A-1MHHi002-A-1MHHi002-A-2MHHi006-A-3MHHi002-A-3 2019-06-11 2019-06-11 PubMed: 31080112 DOI: 10.1016/j.stemcr.2019.04.014Associated cell lines:
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Mendivil-Perez M, Velez-Pardo C, Kosik KS, Lopera F, Jimenez-Del-Rio M
iPSCs-derived nerve-like cells from familial Alzheimer's disease PSEN 1 E280A reveal increased amyloid-beta levels and loss of the Y chromosome
Mendivil-Perez M et al. iPSCs-derived nerve-like cells from familial Alzheimer's disease PSEN 1 E280A reveal increased amyloid-beta levels and loss of the Y chromosome. . 2019-06-11. Pubmed ID: 30904577; DOI: 10.1016/j.neulet.2019.03.032; PMC: PMC7845654 ZZUi010-A 2019-06-11 2019-06-11 PubMed: 30904577 DOI: 10.1016/j.neulet.2019.03.032Associated cell lines:
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Cao X, Yakala GK, van den Hil FE, Cochrane A, Mummery CL, Orlova VV
Differentiation and Functional Comparison of Monocytes and Macrophages from hiPSCs with Peripheral Blood Derivatives
Cao X et al. Differentiation and Functional Comparison of Monocytes and Macrophages from hiPSCs with Peripheral Blood Derivatives. . 2019-06-11. Pubmed ID: 31189095; DOI: 10.1016/j.stemcr.2019.05.003; PMC: PMC6565887 LUMCi001-A 2019-06-11 2019-06-11 PubMed: 31189095 DOI: 10.1016/j.stemcr.2019.05.003Associated cell lines:
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Georgomanoli M, Papapetrou EP
Modeling blood diseases with human induced pluripotent stem cells
Georgomanoli M et al. Modeling blood diseases with human induced pluripotent stem cells. . 2019-06-04. Pubmed ID: 31171568; DOI: 10.1242/dmm.039321; PMC: PMC6602313 CHOPi001-A 2019-06-04 2019-06-04 PubMed: 31171568 DOI: 10.1242/dmm.039321Associated cell lines:
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Lach MS, Wroblewska J, Kulcenty K, Richter M, Trzeciak T, Suchorska WM
Chondrogenic Differentiation of Pluripotent Stem Cells under Controllable Serum-Free Conditions
Lach MS et al. Chondrogenic Differentiation of Pluripotent Stem Cells under Controllable Serum-Free Conditions. . 2019-06-02. Pubmed ID: 31159483; DOI: 10.3390/ijms20112711; PMC: PMC6600514 GPCCi001-A 2019-06-02 2019-06-02 PubMed: 31159483 DOI: 10.3390/ijms20112711Associated cell lines:
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Uniyal AP, Mansotra K, Yadav SK, Kumar V
An overview of designing and selection of sgRNAs for precise genome editing by the CRISPR-Cas9 system in plants
Uniyal AP et al. An overview of designing and selection of sgRNAs for precise genome editing by the CRISPR-Cas9 system in plants. . 2019-06-00. Pubmed ID: 31139538; DOI: 10.1007/s13205-019-1760-2; PMC: PMC6529479 WAe001-ACSCRMi001-AWAe001-A-16 2019-06-00 2019-06-00 PubMed: 31139538 DOI: 10.1007/s13205-019-1760-2Associated cell lines:
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Meents JE, Bressan E, Sontag S, Foerster A, Hautvast P, Rösseler C, Hampl M, Schüler H, Goetzke R, Le TKC, Kleggetveit IP, Le Cann K, Kerth C, Rush AM, Rogers M, Kohl Z, Schmelz M, Wagner W, Jørum E, Namer B, Winner B, Zenke M, Lampert A
The role of Nav1.7 in human nociceptors: insights from human induced pluripotent stem cell-derived sensory neurons of erythromelalgia patients
Meents JE et al. The role of Nav1.7 in human nociceptors: insights from human induced pluripotent stem cell-derived sensory neurons of erythromelalgia patients. . 2019-06-00. Pubmed ID: 30720580; DOI: 10.1097/j.pain.0000000000001511; PMC: PMC6554007 UKAi005-AUKAi006-A 2019-06-00 2019-06-00 PubMed: 30720580 DOI: 10.1097/j.pain.0000000000001511 -
de Graaf MNS, Cochrane A, van den Hil FE, Buijsman W, van der Meer AD, van den Berg A, Mummery CL, Orlova VV
Scalable microphysiological system to model three-dimensional blood vessels
de Graaf MNS et al. Scalable microphysiological system to model three-dimensional blood vessels. . 2019-06-00. Pubmed ID: 31263797; DOI: 10.1063/1.5090986; PMC: PMC6588522 CRMi003-A 2019-06-00 2019-06-00 PubMed: 31263797 DOI: 10.1063/1.5090986Associated cell lines:
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Lin H, Shangguan Z, Zhu M, Bao L, Zhang Q, Pan S
lncRNA FLVCR1-AS1 silencing inhibits lung cancer cell proliferation, migration, and invasion by inhibiting the activity of the Wnt/β-catenin signaling pathway
Lin H et al. lncRNA FLVCR1-AS1 silencing inhibits lung cancer cell proliferation, migration, and invasion by inhibiting the activity of the Wnt/β-catenin signaling pathway. . 2019-06-00. Pubmed ID: 30697812; DOI: 10.1002/jcb.28352 NERCe003-ANERCe003-A-1 2019-06-00 2019-06-00 PubMed: 30697812 DOI: 10.1002/jcb.28352Associated cell lines:
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Del Carmen Ortuño-Costela M, García-López M, Cerrada V, Gallardo ME
iPSCs: A powerful tool for skeletal muscle tissue engineering
Del Carmen Ortuño-Costela M et al. iPSCs: A powerful tool for skeletal muscle tissue engineering. . 2019-06-00. Pubmed ID: 30933431; DOI: 10.1111/jcmm.14292; PMC: PMC6533516 IISHDOi001-A 2019-06-00 2019-06-00 PubMed: 30933431 DOI: 10.1111/jcmm.14292Associated cell lines:
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Xu M, Shaw G, Murphy M, Barry F
Induced Pluripotent Stem Cell-Derived Mesenchymal Stromal Cells Are Functionally and Genetically Different From Bone Marrow-Derived Mesenchymal Stromal Cells
Xu M et al. Induced Pluripotent Stem Cell-Derived Mesenchymal Stromal Cells Are Functionally and Genetically Different From Bone Marrow-Derived Mesenchymal Stromal Cells. . 2019-06-00. Pubmed ID: 30779868; DOI: 10.1002/stem.2993; PMC: PMC6591688 UMNi001-A 2019-06-00 2019-06-00 PubMed: 30779868 DOI: 10.1002/stem.2993Associated cell lines:
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Sacco AM, Belviso I, Romano V, Carfora A, Schonauer F, Nurzynska D, Montagnani S, Di Meglio F, Castaldo C
Diversity of dermal fibroblasts as major determinant of variability in cell reprogramming
Sacco AM et al. Diversity of dermal fibroblasts as major determinant of variability in cell reprogramming. . 2019-06-00. Pubmed ID: 30980516; DOI: 10.1111/jcmm.14316; PMC: PMC6533477 UKWNLi002-A 2019-06-00 2019-06-00 PubMed: 30980516 DOI: 10.1111/jcmm.14316Associated cell lines:
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Schulze ML, Lemoine MD, Fischer AW, Scherschel K, David R, Riecken K, Hansen A, Eschenhagen T, Ulmer BM
Dissecting hiPSC-CM pacemaker function in a cardiac organoid model
Schulze ML et al. Dissecting hiPSC-CM pacemaker function in a cardiac organoid model. . 2019-06-00. Pubmed ID: 30933775; DOI: 10.1016/j.biomaterials.2019.03.023 UKEi003-C 2019-06-00 2019-06-00 PubMed: 30933775 DOI: 10.1016/j.biomaterials.2019.03.023Associated cell lines:
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Quinn PM, Buck TM, Mulder AA, Ohonin C, Alves CH, Vos RM, Bialecka M, van Herwaarden T, van Dijk EHC, Talib M, Freund C, Mikkers HMM, Hoeben RC, Goumans MJ, Boon CJF, Koster AJ, Chuva de Sousa Lopes SM, Jost CR, Wijnholds J
Human iPSC-Derived Retinas Recapitulate the Fetal CRB1 CRB2 Complex Formation and Demonstrate that Photoreceptors and Müller Glia Are Targets of AAV5
Quinn PM et al. Human iPSC-Derived Retinas Recapitulate the Fetal CRB1 CRB2 Complex Formation and Demonstrate that Photoreceptors and Müller Glia Are Targets of AAV5. . 2019-05-14. Pubmed ID: 30956116; DOI: 10.1016/j.stemcr.2019.03.002; PMC: PMC6522954 LUMCi055-ALUMCi056-ALUMCi054-A-2 2019-05-14 2019-05-14 PubMed: 30956116 DOI: 10.1016/j.stemcr.2019.03.002Associated cell lines:
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Matheus F, Rusha E, Rehimi R, Molitor L, Pertek A, Modic M, Feederle R, Flatley A, Kremmer E, Geerlof A, Rishko V, Rada-Iglesias A, Drukker M
Pathological ASXL1 Mutations and Protein Variants Impair Neural Crest Development
Matheus F et al. Pathological ASXL1 Mutations and Protein Variants Impair Neural Crest Development. . 2019-05-14. Pubmed ID: 31006630; DOI: 10.1016/j.stemcr.2019.03.006; PMC: PMC6524927 ISFi001-A 2019-05-14 2019-05-14 PubMed: 31006630 DOI: 10.1016/j.stemcr.2019.03.006Associated cell lines:
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Falzarano MS, Ferlini A
Urinary Stem Cells as Tools to Study Genetic Disease: Overview of the Literature
Falzarano MS et al. Urinary Stem Cells as Tools to Study Genetic Disease: Overview of the Literature. . 2019-05-08. Pubmed ID: 31071994; DOI: 10.3390/jcm8050627; PMC: PMC6572423 ZZUi004-A 2019-05-08 2019-05-08 PubMed: 31071994 DOI: 10.3390/jcm8050627Associated cell lines:
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Baskfield A, Li R, Beers J, Zou J, Liu C, Zheng W
Generation of an induced pluripotent stem cell line (TRNDi004-I) from a Niemann-Pick disease type B patient carrying a heterozygous mutation of p.L43_A44delLA in the SMPD1 gene
Baskfield A et al. Generation of an induced pluripotent stem cell line (TRNDi004-I) from a Niemann-Pick disease type B patient carrying a heterozygous mutation of p.L43_A44delLA in the SMPD1 gene. . 2019-05-00. Pubmed ID: 31009819; DOI: 10.1016/j.scr.2019.101436; PMC: PMC6643268 TRNDi004-I 2019-05-00 2019-05-00 PubMed: 31009819 DOI: 10.1016/j.scr.2019.101436Associated cell lines:
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Bikkuzin T, Shi Y, Sun B, Guo Y, Jin X, Han Z, Pavlov V, Zhang H
Human induced pluripotent stem cell line HMUi001-A derived from corneal stromal cells
Bikkuzin T et al. Human induced pluripotent stem cell line HMUi001-A derived from corneal stromal cells. . 2019-05-00. Pubmed ID: 31121475; DOI: 10.1016/j.scr.2019.101409 HMUi001-A 2019-05-00 2019-05-00 PubMed: 31121475 DOI: 10.1016/j.scr.2019.101409Associated cell lines:
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Lenz D, Staufner C, Wächter S, Hagedorn M, Ebersold J, Göhring G, Kölker S, Hoffmann GF, Jung-Klawitter S
Generation of an induced pluripotent stem cell (iPSC) line, DHMCi005-A, from a patient with CALFAN syndrome due to mutations in SCYL1
Lenz D et al. Generation of an induced pluripotent stem cell (iPSC) line, DHMCi005-A, from a patient with CALFAN syndrome due to mutations in SCYL1. . 2019-05-00. Pubmed ID: 30959346; DOI: 10.1016/j.scr.2019.101428 DHMCi005-A 2019-05-00 2019-05-00 PubMed: 30959346 DOI: 10.1016/j.scr.2019.101428Associated cell lines:
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Ross S, Holliday M, Lim S, Semsarian C
Characterization of the first induced pluripotent stem cell line generated from a patient with autosomal dominant catecholaminergic polymorphic ventricular tachycardia due to a heterozygous mutation in cardiac calsequestrin-2
Ross S et al. Characterization of the first induced pluripotent stem cell line generated from a patient with autosomal dominant catecholaminergic polymorphic ventricular tachycardia due to a heterozygous mutation in cardiac calsequestrin-2. . 2019-05-00. Pubmed ID: 31039485; DOI: 10.1016/j.scr.2019.101450 CIAUi003-A 2019-05-00 2019-05-00 PubMed: 31039485 DOI: 10.1016/j.scr.2019.101450Associated cell lines:
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Arasala RR, Jayaram M, Chattai J, Kumarasamy T, Sambasivan R, Rampalli S
Characterization of new variant human ES line VH9 hESC (INSTEMe001-a): a tool for human stem cell and cancer research
Arasala RR et al. Characterization of new variant human ES line VH9 hESC (INSTEMe001-a): a tool for human stem cell and cancer research. . 2019-05-00. Pubmed ID: 31075691; DOI: 10.1016/j.scr.2019.101444 WAe009-A-G 2019-05-00 2019-05-00 PubMed: 31075691 DOI: 10.1016/j.scr.2019.101444Associated cell lines:
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Yuan X, Li C, Chen X, Liu L, Liu G, Wen F
A Study of Congenital Protein C Deficiency With Infancy Onset of CADASIL in a Chinese Baby
Yuan X et al. A Study of Congenital Protein C Deficiency With Infancy Onset of CADASIL in a Chinese Baby. . 2019-05-00. Pubmed ID: 30883460; DOI: 10.1097/mph.0000000000001436; PMC: PMC6493701 IDISi001-A 2019-05-00 2019-05-00 PubMed: 30883460 DOI: 10.1097/mph.0000000000001436Associated cell lines:
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Hong J, Xu M, Li R, Cheng YS, Kouznetsova J, Beers J, Liu C, Zou J, Zheng W
Generation of an induced pluripotent stem cell line (TRNDi008-A) from a Hunter syndrome patient carrying a hemizygous 208insC mutation in the IDS gene
Hong J et al. Generation of an induced pluripotent stem cell line (TRNDi008-A) from a Hunter syndrome patient carrying a hemizygous 208insC mutation in the IDS gene. . 2019-05-00. Pubmed ID: 31071499; DOI: 10.1016/j.scr.2019.101451; PMC: PMC6642610 TRNDi002-BTRNDi008-A 2019-05-00 2019-05-00 PubMed: 31071499 DOI: 10.1016/j.scr.2019.101451Associated cell lines:
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Vallejo-Diez S, Fleischer A, Martín-Fernández JM, Sánchez-Gilabert A, Castresana M, Aguillón D, Villegas A, Mastronardi CA, Espinosa LG, Arcos-Burgos M, Del Pozo Á, Herrán E, Gainza E, Isaza-Ruget M, Lopera F, Bachiller D
Generation of one iPSC line (IMEDEAi006-A) from an early-onset familial Alzheimer's Disease (fAD) patient carrying the E280A mutation in the PSEN1 gene
Vallejo-Diez S et al. Generation of one iPSC line (IMEDEAi006-A) from an early-onset familial Alzheimer's Disease (fAD) patient carrying the E280A mutation in the PSEN1 gene. . 2019-05-00. Pubmed ID: 31026686; DOI: 10.1016/j.scr.2019.101440 IMEDEAi006-A 2019-05-00 2019-05-00 PubMed: 31026686 DOI: 10.1016/j.scr.2019.101440Associated cell lines:
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Sato T, Migita O, Hata H, Okamoto A, Hata K
Analysis of chromosome microstructures in products of conception associated with recurrent miscarriage
Sato T et al. Analysis of chromosome microstructures in products of conception associated with recurrent miscarriage. . 2019-05-00. Pubmed ID: 30926177; DOI: 10.1016/j.rbmo.2018.12.010 RCe015-A 2019-05-00 2019-05-00 PubMed: 30926177 DOI: 10.1016/j.rbmo.2018.12.010Associated cell lines:
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Cheng YC, Lin HI, Syu SH, Lu HE, Huang CY, Lin CH, Hsieh PCH
Reprogramming of a human induced pluripotent stem cell (iPSC) line (IBMSi012-A) from an early-onset Parkinson's disease patient harboring a homozygous p.D331Y mutation in the PLA2G6 gene
Cheng YC et al. Reprogramming of a human induced pluripotent stem cell (iPSC) line (IBMSi012-A) from an early-onset Parkinson's disease patient harboring a homozygous p.D331Y mutation in the PLA2G6 gene. . 2019-05-00. Pubmed ID: 30978640; DOI: 10.1016/j.scr.2019.101432 IBMSi012-A 2019-05-00 2019-05-00 PubMed: 30978640 DOI: 10.1016/j.scr.2019.101432Associated cell lines:
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Zhang X, Moon SY, Zhang D, Chen SC, Lamey T, Thompson JA, McLaren T, De Roach JN, McLenachan S, Chen FK
Generation of an induced pluripotent stem cell line from a patient with retinitis pigmentosa caused by RP1 mutation
Zhang X et al. Generation of an induced pluripotent stem cell line from a patient with retinitis pigmentosa caused by RP1 mutation. . 2019-05-00. Pubmed ID: 31059986; DOI: 10.1016/j.scr.2019.101452 LEIi005-B 2019-05-00 2019-05-00 PubMed: 31059986 DOI: 10.1016/j.scr.2019.101452Associated cell lines:
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Mura M, Lee YK, Pisano F, Ginevrino M, Boni M, Calabrò F, Crotti L, Valente EM, Schwartz PJ, Tse HF, Gnecchi M
Generation of the human induced pluripotent stem cell (hiPSC) line PSMi005-A from a patient carrying the KCNQ1-R190W mutation
Mura M et al. Generation of the human induced pluripotent stem cell (hiPSC) line PSMi005-A from a patient carrying the KCNQ1-R190W mutation. . 2019-05-00. Pubmed ID: 31009818; DOI: 10.1016/j.scr.2019.101437 PSMi005-A 2019-05-00 2019-05-00 PubMed: 31009818 DOI: 10.1016/j.scr.2019.101437Associated cell lines:
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Mura M, Lee YK, Pisano F, Ginevrino M, Boni M, Calabrò F, Crotti L, Valente EM, Schwartz PJ, Tse HF, Gnecchi M
Generation of the human induced pluripotent stem cell (hiPSC) line PSMi004-A from a carrier of the KCNQ1-R594Q mutation
Mura M et al. Generation of the human induced pluripotent stem cell (hiPSC) line PSMi004-A from a carrier of the KCNQ1-R594Q mutation. . 2019-05-00. Pubmed ID: 30974404; DOI: 10.1016/j.scr.2019.101431 PSMi004-A 2019-05-00 2019-05-00 PubMed: 30974404 DOI: 10.1016/j.scr.2019.101431Associated cell lines:
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Gubert F, Vasques JF, Cozendey TD, Domizi P, Toledo MF, Kasai-Brunswick TH, Loureiro MPS, Lima JMB, Gress CH, Cabello GMK, Cabello PH, Borgonovo T, Vaz IM, Silva R, Mendez-Otero R
Generation of four patient-specific pluripotent induced stem cell lines from two Brazilian patients with amyotrophic lateral sclerosis and two healthy subjects
Gubert F et al. Generation of four patient-specific pluripotent induced stem cell lines from two Brazilian patients with amyotrophic lateral sclerosis and two healthy subjects. . 2019-05-00. Pubmed ID: 31077962; DOI: 10.1016/j.scr.2019.101448 UFRJi005-AUFRJi006-AUFRJi008-AUFRJi009-A 2019-05-00 2019-05-00 PubMed: 31077962 DOI: 10.1016/j.scr.2019.101448Associated cell lines:
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Cheng YS, Li R, Baskfield A, Beers J, Zou J, Liu C, Zheng W
A human induced pluripotent stem cell line (TRNDi007-B) from an infantile onset Pompe patient carrying p.R854X mutation in the GAA gene
Cheng YS et al. A human induced pluripotent stem cell line (TRNDi007-B) from an infantile onset Pompe patient carrying p.R854X mutation in the GAA gene. . 2019-05-00. Pubmed ID: 31026687; DOI: 10.1016/j.scr.2019.101435; PMC: PMC6658133 TRNDi007-B 2019-05-00 2019-05-00 PubMed: 31026687 DOI: 10.1016/j.scr.2019.101435Associated cell lines:
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Sala L, Gnecchi M, Schwartz PJ
Long QT Syndrome Modelling with Cardiomyocytes Derived from Human-induced Pluripotent Stem Cells
Sala L et al. Long QT Syndrome Modelling with Cardiomyocytes Derived from Human-induced Pluripotent Stem Cells. . 2019-05-00. Pubmed ID: 31114684; DOI: 10.15420/aer.2019.1.1; PMC: PMC6528025 PSMi003-A 2019-05-00 2019-05-00 PubMed: 31114684 DOI: 10.15420/aer.2019.1.1Associated cell lines:
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Montes R, Mollinedo P, Perales S, Gonzalez-Lamuño D, Ramos-Mejía V, Fernandez-Luna JL, Real PJ
GENYOi004-A: An induced pluripotent stem cells (iPSCs) line generated from a patient with autism-related ADNP syndrome carrying a pTyr719* mutation
Montes R et al. GENYOi004-A: An induced pluripotent stem cells (iPSCs) line generated from a patient with autism-related ADNP syndrome carrying a pTyr719* mutation. . 2019-05-00. Pubmed ID: 31035039; DOI: 10.1016/j.scr.2019.101446 GENYOi003-AGENYOi004-A 2019-05-00 2019-05-00 PubMed: 31035039 DOI: 10.1016/j.scr.2019.101446Associated cell lines:
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Lu CY, Chen YA, Syu SH, Lu HE, Ho HN, Chen HF
Generation of induced pluripotent stem cell line-NTUHi001-A from a premature ovarian failure patient with Turner's syndrome mosaicism
Lu CY et al. Generation of induced pluripotent stem cell line-NTUHi001-A from a premature ovarian failure patient with Turner's syndrome mosaicism. . 2019-05-00. Pubmed ID: 31004936; DOI: 10.1016/j.scr.2019.101422 NTUHi001-A 2019-05-00 2019-05-00 PubMed: 31004936 DOI: 10.1016/j.scr.2019.101422Associated cell lines:
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Kolundzic N, Khurana P, Hobbs C, Rogar M, Ropret S, Törmä H, Ilic D, Liovic M
Induced pluripotent stem cell (iPSC) line from an epidermolysis bullosa simplex patient heterozygous for keratin 5 E475G mutation and with the Dowling Meara phenotype
Kolundzic N et al. Induced pluripotent stem cell (iPSC) line from an epidermolysis bullosa simplex patient heterozygous for keratin 5 E475G mutation and with the Dowling Meara phenotype. . 2019-05-00. Pubmed ID: 30933721; DOI: 10.1016/j.scr.2019.101424 MLi002-A 2019-05-00 2019-05-00 PubMed: 30933721 DOI: 10.1016/j.scr.2019.101424Associated cell lines:
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Huang W, Xu M, Li R, Baskfield A, Kouznetsova J, Beers J, Zou J, Liu C, Zheng W
An induced pluripotent stem cell line (TRNDi006-A) from a MPS IIIB patient carrying homozygous mutation of p.Glu153Lys in the NAGLU gene
Huang W et al. An induced pluripotent stem cell line (TRNDi006-A) from a MPS IIIB patient carrying homozygous mutation of p.Glu153Lys in the NAGLU gene. . 2019-05-00. Pubmed ID: 30933722; DOI: 10.1016/j.scr.2019.101427; PMC: PMC6559735 TRNDi002-BTRNDi006-A 2019-05-00 2019-05-00 PubMed: 30933722 DOI: 10.1016/j.scr.2019.101427Associated cell lines:
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Lin HI, Cheng YC, Ko HW, Wen CH, Lu HE, Huang CY, Hsieh PCH, Lin CH
Generation of induced pluripotent stem cells (IBMSi011-A) from a patient with Parkinson's disease carrying LRRK2 p.I1371V mutation
Lin HI et al. Generation of induced pluripotent stem cells (IBMSi011-A) from a patient with Parkinson's disease carrying LRRK2 p.I1371V mutation. . 2019-05-00. Pubmed ID: 31029016; DOI: 10.1016/j.scr.2019.101447 IBMSi011-A 2019-05-00 2019-05-00 PubMed: 31029016 DOI: 10.1016/j.scr.2019.101447Associated cell lines:
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Schwarz N, Uysal B, Rosa F, Löffler H, Mau-Holzmann UA, Liebau S, Lerche H
Establishment of a human induced pluripotent stem cell (iPSC) line (HIHDNEi002-A) from a patient with developmental and epileptic encephalopathy carrying a KCNA2 (p.Arg297Gln) mutation
Schwarz N et al. Establishment of a human induced pluripotent stem cell (iPSC) line (HIHDNEi002-A) from a patient with developmental and epileptic encephalopathy carrying a KCNA2 (p.Arg297Gln) mutation. . 2019-05-00. Pubmed ID: 31075689; DOI: 10.1016/j.scr.2019.101445 HIHDNEi002-A 2019-05-00 2019-05-00 PubMed: 31075689 DOI: 10.1016/j.scr.2019.101445Associated cell lines:
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Auboyer L, Monzo C, Wallon D, Rovelet-Lecrux A, Gabelle A, Gazagne I, Cacheux V, Lehmann S, Crozet C
Generation of induced pluripotent stem cells (iPSCs) IRMBi002-A from an Alzheimer's disease patient carrying a D694N mutation in the APP gene
Auboyer L et al. Generation of induced pluripotent stem cells (iPSCs) IRMBi002-A from an Alzheimer's disease patient carrying a D694N mutation in the APP gene. . 2019-05-00. Pubmed ID: 31004935; DOI: 10.1016/j.scr.2019.101438 IRMBi002-A 2019-05-00 2019-05-00 PubMed: 31004935 DOI: 10.1016/j.scr.2019.101438Associated cell lines:
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Hosseini Far H, Patria YN, Motazedian A, Elefanty AG, Stanley EG, Lamandé SR, Bateman JF
Generation of a heterozygous COL1A1 (c.3969_3970insT) osteogenesis imperfecta mutation human iPSC line, MCRIi001-A-1, using CRISPR/Cas9 editing
Hosseini Far H et al. Generation of a heterozygous COL1A1 (c.3969_3970insT) osteogenesis imperfecta mutation human iPSC line, MCRIi001-A-1, using CRISPR/Cas9 editing. . 2019-05-00. Pubmed ID: 31075690; DOI: 10.1016/j.scr.2019.101449 MCRIi001-AMCRIi001-A-1 2019-05-00 2019-05-00 PubMed: 31075690 DOI: 10.1016/j.scr.2019.101449Associated cell lines:
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Trakarnsanga K, Ferguson D, Daniels DE, Griffiths RE, Wilson MC, Mordue KE, Gartner A, Andrienko TN, Calvert A, Condie A, McCahill A, Mountford JC, Toye AM, Anstee DJ, Frayne J
Vimentin expression is retained in erythroid cells differentiated from human iPSC and ESC and indicates dysregulation in these cells early in differentiation
Trakarnsanga K et al. Vimentin expression is retained in erythroid cells differentiated from human iPSC and ESC and indicates dysregulation in these cells early in differentiation. . 2019-04-29. Pubmed ID: 31036072; DOI: 10.1186/s13287-019-1231-z; PMC: PMC6489253 RCe013-A 2019-04-29 2019-04-29 PubMed: 31036072 DOI: 10.1186/s13287-019-1231-zAssociated cell lines:
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Jarosz-Griffiths HH, Corbett NJ, Rowland HA, Fisher K, Jones AC, Baron J, Howell GJ, Cowley SA, Chintawar S, Cader MZ, Kellett KAB, Hooper NM
Proteolytic shedding of the prion protein via activation of metallopeptidase ADAM10 reduces cellular binding and toxicity of amyloid-β oligomers
Jarosz-Griffiths HH et al. Proteolytic shedding of the prion protein via activation of metallopeptidase ADAM10 reduces cellular binding and toxicity of amyloid-β oligomers. . 2019-04-26. Pubmed ID: 30872401; DOI: 10.1074/jbc.ra118.005364; PMC: PMC6497954 UOXFi004-B 2019-04-26 2019-04-26 PubMed: 30872401 DOI: 10.1074/jbc.ra118.005364Associated cell lines:
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Khandany Bardia, Heidari Mohammad Mehdi, Khatami Mehri
Induced pluripotent stem cells (iPSCs) based approaches for hematopoietic cancer therapy
Khandany Bardia et al. Induced pluripotent stem cells (iPSCs) based approaches for hematopoietic cancer therapy. . 2019-04-13. DOI: 10.18502/ijpho.v9i2.611 CHOPi001-A 2019-04-13 2019-04-13 DOI: 10.18502/ijpho.v9i2.611Associated cell lines:
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Halaidych OV, Cochrane A, van den Hil FE, Mummery CL, Orlova VV
Quantitative Analysis of Intracellular Ca(2+) Release and Contraction in hiPSC-Derived Vascular Smooth Muscle Cells
Halaidych OV et al. Quantitative Analysis of Intracellular Ca(2+) Release and Contraction in hiPSC-Derived Vascular Smooth Muscle Cells. . 2019-04-09. Pubmed ID: 30853373; DOI: 10.1016/j.stemcr.2019.02.003; PMC: PMC6449838 LUMCi001-A 2019-04-09 2019-04-09 PubMed: 30853373 DOI: 10.1016/j.stemcr.2019.02.003Associated cell lines:
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Bertero A, Fields PA, Ramani V, Bonora G, Yardimci GG, Reinecke H, Pabon L, Noble WS, Shendure J, Murry CE
Dynamics of genome reorganization during human cardiogenesis reveal an RBM20-dependent splicing factory
Bertero A et al. Dynamics of genome reorganization during human cardiogenesis reveal an RBM20-dependent splicing factory. . 2019-04-04. Pubmed ID: 30948719; DOI: 10.1038/s41467-019-09483-5; PMC: PMC6449405 RUESe002-A 2019-04-04 2019-04-04 PubMed: 30948719 DOI: 10.1038/s41467-019-09483-5Associated cell lines:
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Borgohain MP, Haridhasapavalan KK, Dey C, Adhikari P, Thummer RP
An Insight into DNA-free Reprogramming Approaches to Generate Integration-free Induced Pluripotent Stem Cells for Prospective Biomedical Applications
Borgohain MP et al. An Insight into DNA-free Reprogramming Approaches to Generate Integration-free Induced Pluripotent Stem Cells for Prospective Biomedical Applications. . 2019-04-00. Pubmed ID: 30417242; DOI: 10.1007/s12015-018-9861-6 MUSIi006-A 2019-04-00 2019-04-00 PubMed: 30417242 DOI: 10.1007/s12015-018-9861-6Associated cell lines:
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Arellano-Viera E, Zabaleta L, Castaño J, Azkona G, Carvajal-Vergara X, Giorgetti A
Generation of two transgene-free human iPSC lines from CD133(+) cord blood cells
Arellano-Viera E et al. Generation of two transgene-free human iPSC lines from CD133(+) cord blood cells. . 2019-04-00. Pubmed ID: 30878013; DOI: 10.1016/j.scr.2019.101410 ESi007-A 2019-04-00 2019-04-00 PubMed: 30878013 DOI: 10.1016/j.scr.2019.101410Associated cell lines:
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Ma J, Guo R, Song Y, Zhang J, Feng B, Amponsah AE, Kong D, He J, Zhang W, Liu A, Wei L, Shen S, O'Brien T, Cui H
Generation and characterization of a human induced pluripotent stem cell (iPSC) line (HEBHMUi001-A) from a sporadic Parkinson's disease patient
Ma J et al. Generation and characterization of a human induced pluripotent stem cell (iPSC) line (HEBHMUi001-A) from a sporadic Parkinson's disease patient. . 2019-04-00. Pubmed ID: 30875588; DOI: 10.1016/j.scr.2019.101417 HEBHMUi001-A 2019-04-00 2019-04-00 PubMed: 30875588 DOI: 10.1016/j.scr.2019.101417Associated cell lines:
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Mura M, Pisano F, Stefanello M, Ginevrino M, Boni M, Calabrò F, Crotti L, Valente EM, Schwartz PJ, Brink PA, Gnecchi M
Generation of the human induced pluripotent stem cell (hiPSC) line PSMi007-A from a Long QT Syndrome type 1 patient carrier of two common variants in the NOS1AP gene
Mura M et al. Generation of the human induced pluripotent stem cell (hiPSC) line PSMi007-A from a Long QT Syndrome type 1 patient carrier of two common variants in the NOS1AP gene. . 2019-04-00. Pubmed ID: 30878014; DOI: 10.1016/j.scr.2019.101416 PSMi007-A 2019-04-00 2019-04-00 PubMed: 30878014 DOI: 10.1016/j.scr.2019.101416Associated cell lines:
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Li R, Baskfield A, Beers J, Zou J, Liu C, Alméciga-Díaz CJ, Zheng W
Generation of an induced pluripotent stem cell line (TRNDi005-A) from a Mucopolysaccharidosis Type IVA (MPS IVA) patient carrying compound heterozygous p.R61W and p.WT405del mutations in the GALNS gene
Li R et al. Generation of an induced pluripotent stem cell line (TRNDi005-A) from a Mucopolysaccharidosis Type IVA (MPS IVA) patient carrying compound heterozygous p.R61W and p.WT405del mutations in the GALNS gene. . 2019-04-00. Pubmed ID: 30797135; DOI: 10.1016/j.scr.2019.101408; PMC: PMC8045742 TRNDi005-A 2019-04-00 2019-04-00 PubMed: 30797135 DOI: 10.1016/j.scr.2019.101408Associated cell lines:
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Huijbregts L, Petersen MBK, Berthault C, Hansson M, Aiello V, Rachdi L, Grapin-Botton A, Honore C, Scharfmann R
Bromodomain and Extra Terminal Protein Inhibitors Promote Pancreatic Endocrine Cell Fate
Huijbregts L et al. Bromodomain and Extra Terminal Protein Inhibitors Promote Pancreatic Endocrine Cell Fate. . 2019-04-00. Pubmed ID: 30655386; DOI: 10.2337/db18-0224 STBCi322-A 2019-04-00 2019-04-00 PubMed: 30655386 DOI: 10.2337/db18-0224Associated cell lines:
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Garreta E, Prado P, Tarantino C, Oria R, Fanlo L, Martí E, Zalvidea D, Trepat X, Roca-Cusachs P, Gavaldà-Navarro A, Cozzuto L, Campistol JM, Izpisúa Belmonte JC, Hurtado Del Pozo C, Montserrat N
Fine tuning the extracellular environment accelerates the derivation of kidney organoids from human pluripotent stem cells
Garreta E et al. Fine tuning the extracellular environment accelerates the derivation of kidney organoids from human pluripotent stem cells. . 2019-04-00. Pubmed ID: 30778227; DOI: 10.1038/s41563-019-0287-6; PMC: PMC9845070 ESe014-AESi007-A 2019-04-00 2019-04-00 PubMed: 30778227 DOI: 10.1038/s41563-019-0287-6 -
Suga M, Kondo T, Imamura K, Shibukawa R, Okanishi Y, Sagara Y, Tsukita K, Enami T, Furujo M, Saijo K, Nakamura Y, Osawa M, Saito MK, Yamanaka S, Inoue H
Generation of a human induced pluripotent stem cell line, BRCi001-A, derived from a patient with mucopolysaccharidosis type I
Suga M et al. Generation of a human induced pluripotent stem cell line, BRCi001-A, derived from a patient with mucopolysaccharidosis type I. . 2019-04-00. Pubmed ID: 30849633; DOI: 10.1016/j.scr.2019.101406 BRCi001-A 2019-04-00 2019-04-00 PubMed: 30849633 DOI: 10.1016/j.scr.2019.101406Associated cell lines:
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Xu J, Fu Y, Xia W, He J, Zou Y, Ruan W, Lou Q, Li Y, Pan J, Li H, Chen W
Generation of induced pluripotent stem cell line, ZJUCHi002-A, from Charcot-Marie-Tooth disease type 2A (CMT2A) patient with a mutation of c.752C>T in MFN2
Xu J et al. Generation of induced pluripotent stem cell line, ZJUCHi002-A, from Charcot-Marie-Tooth disease type 2A (CMT2A) patient with a mutation of c.752C>T in MFN2. . 2019-04-00. Pubmed ID: 30807887; DOI: 10.1016/j.scr.2019.101411 ZJUCHi002-A 2019-04-00 2019-04-00 PubMed: 30807887 DOI: 10.1016/j.scr.2019.101411Associated cell lines:
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Riera M, Patel A, Burés-Jelstrup A, Corcostegui B, Chang S, Pomares E, Corneo B, Sparrow JR
Generation of two iPS cell lines (FRIMOi003-A and FRIMOi004-A) derived from Stargardt patients carrying ABCA4 compound heterozygous mutations
Riera M et al. Generation of two iPS cell lines (FRIMOi003-A and FRIMOi004-A) derived from Stargardt patients carrying ABCA4 compound heterozygous mutations. . 2019-04-00. Pubmed ID: 30798147; DOI: 10.1016/j.scr.2019.101389; PMC: PMC6668028 FRIMOi003-AFRIMOi004-A 2019-04-00 2019-04-00 PubMed: 30798147 DOI: 10.1016/j.scr.2019.101389Associated cell lines:
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Cederquist GY, Asciolla JJ, Tchieu J, Walsh RM, Cornacchia D, Resh MD, Studer L
Specification of positional identity in forebrain organoids
Cederquist GY et al. Specification of positional identity in forebrain organoids. . 2019-04-00. Pubmed ID: 30936566; DOI: 10.1038/s41587-019-0085-3; PMC: PMC6447454 WAe009-A-1W 2019-04-00 2019-04-00 PubMed: 30936566 DOI: 10.1038/s41587-019-0085-3Associated cell lines:
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Li X, Dong T, Li Y, Wu F, Lan F
Generation of a human iPSC line from a patient with Marfan syndrome caused by mutation in FBN1
Li X et al. Generation of a human iPSC line from a patient with Marfan syndrome caused by mutation in FBN1. . 2019-04-00. Pubmed ID: 30870686; DOI: 10.1016/j.scr.2019.101414 CMUi001-A 2019-04-00 2019-04-00 PubMed: 30870686 DOI: 10.1016/j.scr.2019.101414Associated cell lines:
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Buijsen RAM, Toonen LJA, Gardiner SL, van Roon-Mom WMC
Genetics, Mechanisms, and Therapeutic Progress in Polyglutamine Spinocerebellar Ataxias
Buijsen RAM et al. Genetics, Mechanisms, and Therapeutic Progress in Polyglutamine Spinocerebellar Ataxias. . 2019-04-00. Pubmed ID: 30607747; DOI: 10.1007/s13311-018-00696-y; PMC: PMC6554265 LUMCi002-ALUMCi003-A 2019-04-00 2019-04-00 PubMed: 30607747 DOI: 10.1007/s13311-018-00696-yAssociated cell lines:
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de la Cerda B, Díez-Lloret A, Ponte B, Vallés-Saiz L, Calado SM, Rodríguez-Bocanegra E, Garcia-Delgado AB, Moya-Molina M, Bhattacharya SS, Díaz-Corrales FJ
Generation and characterization of the human iPSC line CABi001-A from a patient with retinitis pigmentosa caused by a novel mutation in PRPF31 gene
de la Cerda B et al. Generation and characterization of the human iPSC line CABi001-A from a patient with retinitis pigmentosa caused by a novel mutation in PRPF31 gene. . 2019-04-00. Pubmed ID: 30921587; DOI: 10.1016/j.scr.2019.101426 ESi077-A 2019-04-00 2019-04-00 PubMed: 30921587 DOI: 10.1016/j.scr.2019.101426Associated cell lines:
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Farkhondeh A, Li R, Gorshkov K, Chen KG, Might M, Rodems S, Lo DC, Zheng W
Induced pluripotent stem cells for neural drug discovery
Farkhondeh A et al. Induced pluripotent stem cells for neural drug discovery. . 2019-04-00. Pubmed ID: 30664937; DOI: 10.1016/j.drudis.2019.01.007; PMC: PMC6476685 TRNDi002-B 2019-04-00 2019-04-00 PubMed: 30664937 DOI: 10.1016/j.drudis.2019.01.007Associated cell lines:
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Wang Y, Zhang J, Hu J, Li G, Lei Y, Zhao J
Establishment of TUSMi008-A, an induced pluripotent stem cell (iPSC) line from a 76-year old Alzheimer's disease (AD) patient with PAXIP1 gene mutation
Wang Y et al. Establishment of TUSMi008-A, an induced pluripotent stem cell (iPSC) line from a 76-year old Alzheimer's disease (AD) patient with PAXIP1 gene mutation. . 2019-04-00. Pubmed ID: 30831521; DOI: 10.1016/j.scr.2019.101391 TUSMi008-A 2019-04-00 2019-04-00 PubMed: 30831521 DOI: 10.1016/j.scr.2019.101391Associated cell lines:
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Jung-Klawitter S, Wächter S, Hagedorn M, Ebersold J, Göhring G, Opladen T
Generation of 2 iPSC clones from a patient with DNAJC12 deficiency: DHMCi003-A and DHMCi003-B
Jung-Klawitter S et al. Generation of 2 iPSC clones from a patient with DNAJC12 deficiency: DHMCi003-A and DHMCi003-B. . 2019-04-00. Pubmed ID: 30901742; DOI: 10.1016/j.scr.2019.101402 DHMCi003-ADHMCi003-B 2019-04-00 2019-04-00 PubMed: 30901742 DOI: 10.1016/j.scr.2019.101402Associated cell lines:
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Wang Y, Zhang J, Lei Y, Zhao J
Corrigendum to "Establishment of TUSMi007-A, an induced pluripotent stem cell (iPSC) line from an 83-year old Chinese Han patient with Alzheimer's disease (AD)" [Stem Cell Research 33(2018) 265-268]
Wang Y et al. Corrigendum to "Establishment of TUSMi007-A, an induced pluripotent stem cell (iPSC) line from an 83-year old Chinese Han patient with Alzheimer's disease (AD)" [Stem Cell Research 33(2018) 265-268]. . 2019-04-00. Pubmed ID: 30826348; DOI: 10.1016/j.scr.2019.101412 TUSMi007-A 2019-04-00 2019-04-00 PubMed: 30826348 DOI: 10.1016/j.scr.2019.101412Associated cell lines:
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Grigor'eva EV, Malankhanova TB, Ustyantseva EI, Minina JM, Redina OE, Morozov VV, Shevela AI, Zakian SM, Medvedev SP
Generation of two iPSC lines (ICGi008-A and ICGi008-B) from skin fibroblasts of a patient with early-onset Alzheimer's disease caused by London familial APP mutation (V717I)
Grigor'eva EV et al. Generation of two iPSC lines (ICGi008-A and ICGi008-B) from skin fibroblasts of a patient with early-onset Alzheimer's disease caused by London familial APP mutation (V717I). . 2019-04-00. Pubmed ID: 30851551; DOI: 10.1016/j.scr.2019.101415 ICGi007-AICGi008-AICGi008-B 2019-04-00 2019-04-00 PubMed: 30851551 DOI: 10.1016/j.scr.2019.101415 -
Zhao J
Corrigendum to Establishment of TUSMi005-A, an induced pluripotent stem cell (iPSC) line from a 32-year old Chinese Han patient with Bipolar Disorder (BD). Stem Cell Research 33(2018) 65-68
Zhao J. Corrigendum to Establishment of TUSMi005-A, an induced pluripotent stem cell (iPSC) line from a 32-year old Chinese Han patient with Bipolar Disorder (BD). Stem Cell Research 33(2018) 65-68. . 2019-04-00. Pubmed ID: 30826347; DOI: 10.1016/j.scr.2019.101413 TUSMi005-A 2019-04-00 2019-04-00 PubMed: 30826347 DOI: 10.1016/j.scr.2019.101413Associated cell lines:
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Tangprasittipap A, Jittorntrum B, Kadegasem P, Sasanakul W, Sirachainan N, Kitiyanant N, Hongeng S
Generation of a human induced pluripotent stem cell line (MUi010-A) from skin fibroblast of patient carrying a c.2104C>T mutation in MYH9 gene
Tangprasittipap A et al. Generation of a human induced pluripotent stem cell line (MUi010-A) from skin fibroblast of patient carrying a c.2104C>T mutation in MYH9 gene. . 2019-04-00. Pubmed ID: 30798146; DOI: 10.1016/j.scr.2019.101397 MUi010-A 2019-04-00 2019-04-00 PubMed: 30798146 DOI: 10.1016/j.scr.2019.101397Associated cell lines:
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Klaus J, Kanton S, Kyrousi C, Ayo-Martin AC, Di Giaimo R, Riesenberg S, O'Neill AC, Camp JG, Tocco C, Santel M, Rusha E, Drukker M, Schroeder M, Götz M, Robertson SP, Treutlein B, Cappello S
Altered neuronal migratory trajectories in human cerebral organoids derived from individuals with neuronal heterotopia
Klaus J et al. Altered neuronal migratory trajectories in human cerebral organoids derived from individuals with neuronal heterotopia. . 2019-04-00. Pubmed ID: 30858616; DOI: 10.1038/s41591-019-0371-0 ISFi001-AISFi003-AISFi004-A 2019-04-00 2019-04-00 PubMed: 30858616 DOI: 10.1038/s41591-019-0371-0 -
McLenachan S, Wong EYM, Zhang X, Leith F, Moon SY, Zhang D, Chen SC, Thompson JA, McLaren T, Lamey T, De Roach JN, Atlas MD, Dilley RJ, Chen FK
Generation of two induced pluripotent stem cell lines from a patient with compound heterozygous mutations in the USH2A gene
McLenachan S et al. Generation of two induced pluripotent stem cell lines from a patient with compound heterozygous mutations in the USH2A gene. . 2019-04-00. Pubmed ID: 30904819; DOI: 10.1016/j.scr.2019.101420 LEIi010-ALEIi010-B 2019-04-00 2019-04-00 PubMed: 30904819 DOI: 10.1016/j.scr.2019.101420 -
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Deep Learning-Based Proarrhythmia Analysis Using Field Potentials Recorded From Human Pluripotent Stem Cells Derived Cardiomyocytes.
(unknown author). Deep Learning-Based Proarrhythmia Analysis Using Field Potentials Recorded From Human Pluripotent Stem Cells Derived Cardiomyocytes. . 2019-03-28. UKKi007-AUKKi009-A 2019-03-28 2019-03-28 -
Fenske P, Grauel MK, Brockmann MM, Dorrn AL, Trimbuch T, Rosenmund C
Autaptic cultures of human induced neurons as a versatile platform for studying synaptic function and neuronal morphology
Fenske P et al. Autaptic cultures of human induced neurons as a versatile platform for studying synaptic function and neuronal morphology. . 2019-03-20. Pubmed ID: 30894602; DOI: 10.1038/s41598-019-41259-1; PMC: PMC6427022 BIHi001-ABIHi004-A 2019-03-20 2019-03-20 PubMed: 30894602 DOI: 10.1038/s41598-019-41259-1 -
Devito L, Klontzas ME, Cvoro A, Galleu A, Simon M, Hobbs C, Dazzi F, Mantalaris A, Khalaf Y, Ilic D
Comparison of human isogeneic Wharton's jelly MSCs and iPSC-derived MSCs reveals differentiation-dependent metabolic responses to IFNG stimulation
Devito L et al. Comparison of human isogeneic Wharton's jelly MSCs and iPSC-derived MSCs reveals differentiation-dependent metabolic responses to IFNG stimulation. . 2019-03-20. Pubmed ID: 30894508; DOI: 10.1038/s41419-019-1498-0; PMC: PMC6426992 KCLi001-A 2019-03-20 2019-03-20 PubMed: 30894508 DOI: 10.1038/s41419-019-1498-0Associated cell lines:
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Xiang Y, Tanaka Y, Cakir B, Patterson B, Kim KY, Sun P, Kang YJ, Zhong M, Liu X, Patra P, Lee SH, Weissman SM, Park IH
hESC-Derived Thalamic Organoids Form Reciprocal Projections When Fused with Cortical Organoids
Xiang Y et al. hESC-Derived Thalamic Organoids Form Reciprocal Projections When Fused with Cortical Organoids. . 2019-03-07. Pubmed ID: 30799279; DOI: 10.1016/j.stem.2018.12.015; PMC: PMC6853597 WAe001-A 2019-03-07 2019-03-07 PubMed: 30799279 DOI: 10.1016/j.stem.2018.12.015Associated cell lines:
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Fanning S, Haque A, Imberdis T, Baru V, Barrasa MI, Nuber S, Termine D, Ramalingam N, Ho GPH, Noble T, Sandoe J, Lou Y, Landgraf D, Freyzon Y, Newby G, Soldner F, Terry-Kantor E, Kim TE, Hofbauer HF, Becuwe M, Jaenisch R, Pincus D, Clish CB, Walther TC, Farese RV Jr, Srinivasan S, Welte MA, Kohlwein SD, Dettmer U, Lindquist S, Selkoe D
Lipidomic Analysis of α-Synuclein Neurotoxicity Identifies Stearoyl CoA Desaturase as a Target for Parkinson Treatment
Fanning S et al. Lipidomic Analysis of α-Synuclein Neurotoxicity Identifies Stearoyl CoA Desaturase as a Target for Parkinson Treatment. . 2019-03-07. Pubmed ID: 30527540; DOI: 10.1016/j.molcel.2018.11.028; PMC: PMC6408259 EDi001-AEDi001-A-4 2019-03-07 2019-03-07 PubMed: 30527540 DOI: 10.1016/j.molcel.2018.11.028Associated cell lines:
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Fernandes S, Tembe S, Singh S, Vardhan S, Nair V, Kale V, Limaye L
Erratum to "Development and characterization of human iPSC line NCCSi004-A from umbilical cord blood (UCB) derived CD34 + cells obtained from donor belonging to Indian ethnic population" [Stem Cell Research Volume 35, March 2019, 101,392]
Fernandes S et al. Erratum to "Development and characterization of human iPSC line NCCSi004-A from umbilical cord blood (UCB) derived CD34 + cells obtained from donor belonging to Indian ethnic population" [Stem Cell Research Volume 35, March 2019, 101,392]. . 2019-03-00. Pubmed ID: 30772284; DOI: 10.1016/j.scr.2019.101404 NCCSi004-A 2019-03-00 2019-03-00 PubMed: 30772284 DOI: 10.1016/j.scr.2019.101404Associated cell lines:
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Riera M, Patel A, Corcostegui B, Chang S, Sparrow JR, Pomares E, Corneo B
Establishment and characterization of an iPSC line (FRIMOi001-A) derived from a retinitis pigmentosa patient carrying PDE6A mutations
Riera M et al. Establishment and characterization of an iPSC line (FRIMOi001-A) derived from a retinitis pigmentosa patient carrying PDE6A mutations. . 2019-03-00. Pubmed ID: 30685614; DOI: 10.1016/j.scr.2019.101385 FRIMOi001-A 2019-03-00 2019-03-00 PubMed: 30685614 DOI: 10.1016/j.scr.2019.101385Associated cell lines:
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Kahounová Z, Slabáková E, Binó L, Remšík J, Fedr R, Bouchal J, Vrtěl R, Jurečková L, Porokh V, Páralová D, Hampl A, Souček K
Generation of human iPSCs from fetal prostate fibroblasts HPrF
Kahounová Z et al. Generation of human iPSCs from fetal prostate fibroblasts HPrF. . 2019-03-00. Pubmed ID: 30776675; DOI: 10.1016/j.scr.2019.101405 IBPi001-A 2019-03-00 2019-03-00 PubMed: 30776675 DOI: 10.1016/j.scr.2019.101405Associated cell lines:
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Zhang Q, Li Z, Sun H, Zhang S, Zhang J, Wang Y, Fang H, Xu Y
Generation of induced pluripotent stem cell line (ZZUi0012-A) from a patient with Fahr's disease caused by a novel mutation in SLC20A2 gene
Zhang Q et al. Generation of induced pluripotent stem cell line (ZZUi0012-A) from a patient with Fahr's disease caused by a novel mutation in SLC20A2 gene. . 2019-03-00. Pubmed ID: 30776674; DOI: 10.1016/j.scr.2019.101395 ZZUi012-A 2019-03-00 2019-03-00 PubMed: 30776674 DOI: 10.1016/j.scr.2019.101395Associated cell lines:
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Haase A, Glienke W, Engels L, Göhring G, Esser R, Arseniev L, Martin U
GMP-compatible manufacturing of three iPS cell lines from human peripheral blood
Haase A et al. GMP-compatible manufacturing of three iPS cell lines from human peripheral blood. . 2019-03-00. Pubmed ID: 30772682; DOI: 10.1016/j.scr.2019.101394 MHHi008-AMHHi008-BMHHi008-C 2019-03-00 2019-03-00 PubMed: 30772682 DOI: 10.1016/j.scr.2019.101394 -
Frederiksen HR, Holst B, Mau-Holzmann UA, Freude K, Schmid B
Generation of two isogenic iPSC lines with either a heterozygous or a homozygous E280A mutation in the PSEN1 gene
Frederiksen HR et al. Generation of two isogenic iPSC lines with either a heterozygous or a homozygous E280A mutation in the PSEN1 gene. . 2019-03-00. Pubmed ID: 30769329; DOI: 10.1016/j.scr.2019.101403 BIONi010-C-29BIONi010-C-30 2019-03-00 2019-03-00 PubMed: 30769329 DOI: 10.1016/j.scr.2019.101403Associated cell lines:
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Klein T, Klug K, Henkel L, Kwok CK, Edenhofer F, Klopocki E, Kurth I, Üçeyler N
Generation of two induced pluripotent stem cell lines from skin fibroblasts of sisters carrying a c.1094C>A variation in the SCN10A gene potentially associated with small fiber neuropathy
Klein T et al. Generation of two induced pluripotent stem cell lines from skin fibroblasts of sisters carrying a c.1094C>A variation in the SCN10A gene potentially associated with small fiber neuropathy. . 2019-03-00. Pubmed ID: 30731422; DOI: 10.1016/j.scr.2019.101396 UKWNLi003-AUKWNLi004-A 2019-03-00 2019-03-00 PubMed: 30731422 DOI: 10.1016/j.scr.2019.101396Associated cell lines:
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Fernandes S, Tembe S, Singh S, Vardhan S, Nair V, Kale V, Limaye L
Development and characterization of human iPSC line NCCSi004-A from umbilical cord blood (UCB) derived CD34(+)cells obtained from donor belonging to Indian ethnic population
Fernandes S et al. Development and characterization of human iPSC line NCCSi004-A from umbilical cord blood (UCB) derived CD34(+)cells obtained from donor belonging to Indian ethnic population. . 2019-03-00. Pubmed ID: 30711803; DOI: 10.1016/j.scr.2019.101392 NCCSi004-A 2019-03-00 2019-03-00 PubMed: 30711803 DOI: 10.1016/j.scr.2019.101392Associated cell lines:
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Riera M, Patel A, Corcostegui B, Chang S, Corneo B, Sparrow JR, Pomares E
Generation of an induced pluripotent stem cell line (FRIMOi002-A) from a retinitis pigmentosa patient carrying compound heterozygous mutations in USH2A gene
Riera M et al. Generation of an induced pluripotent stem cell line (FRIMOi002-A) from a retinitis pigmentosa patient carrying compound heterozygous mutations in USH2A gene. . 2019-03-00. Pubmed ID: 30685615; DOI: 10.1016/j.scr.2019.101386 FRIMOi002-A 2019-03-00 2019-03-00 PubMed: 30685615 DOI: 10.1016/j.scr.2019.101386Associated cell lines:
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Eisen B, Ben Jehuda R, Cuttitta AJ, Mekies LN, Shemer Y, Baskin P, Reiter I, Willi L, Freimark D, Gherghiceanu M, Monserrat L, Scherr M, Hilfiker-Kleiner D, Arad M, Michele DE, Binah O
Electrophysiological abnormalities in induced pluripotent stem cell-derived cardiomyocytes generated from Duchenne muscular dystrophy patients
Eisen B et al. Electrophysiological abnormalities in induced pluripotent stem cell-derived cardiomyocytes generated from Duchenne muscular dystrophy patients. . 2019-03-00. Pubmed ID: 30618214; DOI: 10.1111/jcmm.14124; PMC: PMC6378185 IITi001-A 2019-03-00 2019-03-00 PubMed: 30618214 DOI: 10.1111/jcmm.14124Associated cell lines:
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Fang EF, Hou Y, Palikaras K, Adriaanse BA, Kerr JS, Yang B, Lautrup S, Hasan-Olive MM, Caponio D, Dan X, Rocktäschel P, Croteau DL, Akbari M, Greig NH, Fladby T, Nilsen H, Cader MZ, Mattson MP, Tavernarakis N, Bohr VA
Mitophagy inhibits amyloid-β and tau pathology and reverses cognitive deficits in models of Alzheimer's disease
Fang EF et al. Mitophagy inhibits amyloid-β and tau pathology and reverses cognitive deficits in models of Alzheimer's disease. . 2019-03-00. Pubmed ID: 30742114; DOI: 10.1038/s41593-018-0332-9; PMC: PMC6693625 STBCi322-A 2019-03-00 2019-03-00 PubMed: 30742114 DOI: 10.1038/s41593-018-0332-9Associated cell lines:
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Nagel M, Reichbauer J, Böhringer J, Schelling Y, Krägeloh-Mann I, Schüle R, Ulmer U
Generation of two iPSC lines derived from two unrelated patients with Gaucher disease
Nagel M et al. Generation of two iPSC lines derived from two unrelated patients with Gaucher disease. . 2019-03-00. Pubmed ID: 30606667; DOI: 10.1016/j.scr.2018.10.021 HIHRSi001-AHIHRSi002-A 2019-03-00 2019-03-00 PubMed: 30606667 DOI: 10.1016/j.scr.2018.10.021Associated cell lines:
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Wei R, Han H, Ye M, He L, Lei Q, Zhou T, Cai X, Li Z
Generation of an integration-free iPSC line(SYSUi001-A) from a sporadic Alzheimer's disease patient
Wei R et al. Generation of an integration-free iPSC line(SYSUi001-A) from a sporadic Alzheimer's disease patient. . 2019-03-00. Pubmed ID: 30797990; DOI: 10.1016/j.scr.2018.101375 SYSUi001-A 2019-03-00 2019-03-00 PubMed: 30797990 DOI: 10.1016/j.scr.2018.101375Associated cell lines:
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Khudiakov AA, Smolina NA, Perepelina KI, Malashicheva AB, Kostareva AA
Extracellular MicroRNAs and Mitochondrial DNA as Potential Biomarkers of Arrhythmogenic Cardiomyopathy
Khudiakov AA et al. Extracellular MicroRNAs and Mitochondrial DNA as Potential Biomarkers of Arrhythmogenic Cardiomyopathy. . 2019-03-00. Pubmed ID: 31221065; DOI: 10.1134/s000629791903009x FAMRCi001-AFAMRCi003-AFAMRCi001-BFAMRCi003-B 2019-03-00 2019-03-00 PubMed: 31221065 DOI: 10.1134/s000629791903009xAssociated cell lines:
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Lenz D, Staufner C, Wächter S, Hagedorn M, Ebersold J, Göhring G, Kölker S, Hoffmann GF, Jung-Klawitter S
Generation of an iPSC line from a patient with infantile liver failure syndrome 2 due to mutations in NBAS: DHMCi004-A
Lenz D et al. Generation of an iPSC line from a patient with infantile liver failure syndrome 2 due to mutations in NBAS: DHMCi004-A. . 2019-03-00. Pubmed ID: 30772683; DOI: 10.1016/j.scr.2019.101398 DHMCi004-A 2019-03-00 2019-03-00 PubMed: 30772683 DOI: 10.1016/j.scr.2019.101398Associated cell lines:
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Xu J, Wang Y, He J, Xia W, Zou Y, Ruan W, Lou Q, Li Y, Li H, Chen W
Generation of a human Charcot-Marie-Tooth disease type 1B (CMT1B) iPSC line, ZJUCHi001-A, with a mutation of c.292C>T in MPZ
Xu J et al. Generation of a human Charcot-Marie-Tooth disease type 1B (CMT1B) iPSC line, ZJUCHi001-A, with a mutation of c.292C>T in MPZ. . 2019-03-00. Pubmed ID: 30785048; DOI: 10.1016/j.scr.2019.101407 ZJUCHi001-A 2019-03-00 2019-03-00 PubMed: 30785048 DOI: 10.1016/j.scr.2019.101407Associated cell lines:
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Camargo Ortega G, Falk S, Johansson PA, Peyre E, Broix L, Sahu SK, Hirst W, Schlichthaerle T, De Juan Romero C, Draganova K, Vinopal S, Chinnappa K, Gavranovic A, Karakaya T, Steininger T, Merl-Pham J, Feederle R, Shao W, Shi SH, Hauck SM, Jungmann R, Bradke F, Borrell V, Geerlof A, Reber S, Tiwari VK, Huttner WB, Wilsch-Bräuninger M, Nguyen L, Götz M
The centrosome protein AKNA regulates neurogenesis via microtubule organization
Camargo Ortega G et al. The centrosome protein AKNA regulates neurogenesis via microtubule organization. . 2019-03-00. Pubmed ID: 30787442; DOI: 10.1038/s41586-019-0962-4 ISFi001-A 2019-03-00 2019-03-00 PubMed: 30787442 DOI: 10.1038/s41586-019-0962-4Associated cell lines:
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Piovani G, Lanzi G, Ferraro RM, Masneri S, Barisani C, Savio G, Giliani SC
Generation of induced pluripotent stem cells (iPSCs) from patient with Cri du Chat Syndrome
Piovani G et al. Generation of induced pluripotent stem cells (iPSCs) from patient with Cri du Chat Syndrome. . 2019-03-00. Pubmed ID: 30711802; DOI: 10.1016/j.scr.2019.101393 UNIBSi004-A 2019-03-00 2019-03-00 PubMed: 30711802 DOI: 10.1016/j.scr.2019.101393Associated cell lines:
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Hennig AF, Rössler U, Boiti F, von der Hagen M, Gossen M, Kornak U, Stachelscheid H
Generation of a human induced pluripotent stem cell line (BIHi002-A) from a patient with CLCN7-related infantile malignant autosomal recessive osteopetrosis
Hennig AF et al. Generation of a human induced pluripotent stem cell line (BIHi002-A) from a patient with CLCN7-related infantile malignant autosomal recessive osteopetrosis. . 2019-03-00. Pubmed ID: 30763735; DOI: 10.1016/j.scr.2018.101367 BIHi002-A 2019-03-00 2019-03-00 PubMed: 30763735 DOI: 10.1016/j.scr.2018.101367Associated cell lines:
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Vigilante A, Laddach A, Moens N, Meleckyte R, Leha A, Ghahramani A, Culley OJ, Kathuria A, Hurling C, Vickers A, Wiseman E, Tewary M, Zandstra PW, HipSci Consortium, Durbin R, Fraternali F, Stegle O, Birney E, Luscombe NM, Danovi D, Watt FM
Identifying Extrinsic versus Intrinsic Drivers of Variation in Cell Behavior in Human iPSC Lines from Healthy Donors
Vigilante A et al. Identifying Extrinsic versus Intrinsic Drivers of Variation in Cell Behavior in Human iPSC Lines from Healthy Donors. . 2019-02-19. Pubmed ID: 30784590; DOI: 10.1016/j.celrep.2019.01.094; PMC: PMC6381787 WTSIi033-AWTSIi034-AWTSIi035-AWTSIi036-AWTSIi055-AWTSIi068-AWTSIi082-AWTSIi085-AWTSIi098-AWTSIi102-AWTSIi103-AWTSIi104-AWTSIi105-AWTSIi108-AWTSIi106-BWTSIi109-AWTSIi110-AWTSIi102-BWTSIi104-BWTSIi111-AWTSIi112-AWTSIi113-AWTSIi114-AWTSIi115-AWTSIi116-AWTSIi118-AWTSIi119-AWTSIi120-AWTSIi121-AWTSIi121-BWTSIi123-AWTSIi124-AWTSIi124-BWTSIi125-AWTSIi126-AWTSIi127-AWTSIi128-AWTSIi129-AWTSIi109-BWTSIi113-BWTSIi140-AWTSIi141-AWTSIi157-AWTSIi159-AWTSIi206-AWTSIi207-AWTSIi208-AWTSIi209-AWTSIi211-AWTSIi212-AWTSIi213-AWTSIi214-AWTSIi216-AWTSIi217-AWTSIi219-AWTSIi222-AWTSIi223-AWTSIi225-AWTSIi227-AWTSIi232-AWTSIi233-AWTSIi235-AWTSIi236-AWTSIi241-AWTSIi248-AWTSIi279-AWTSIi297-AWTSIi140-BWTSIi116-BWTSIi112-BWTSIi123-BWTSIi141-BWTSIi055-BWTSIi110-BWTSIi111-BWTSIi217-BWTSIi216-BWTSIi212-BWTSIi118-BWTSIi225-BWTSIi117-BWTSIi214-BWTSIi129-BWTSIi213-BWTSIi297-BWTSIi297-CWTSIi297-D 2019-02-19 2019-02-19 PubMed: 30784590 DOI: 10.1016/j.celrep.2019.01.094 -
Velazco-Cruz L, Song J, Maxwell KG, Goedegebuure MM, Augsornworawat P, Hogrebe NJ, Millman JR
Acquisition of Dynamic Function in Human Stem Cell-Derived β Cells
Velazco-Cruz L et al. Acquisition of Dynamic Function in Human Stem Cell-Derived β Cells. . 2019-02-12. Pubmed ID: 30661993; DOI: 10.1016/j.stemcr.2018.12.012; PMC: PMC6372986 HVRDi007-A 2019-02-12 2019-02-12 PubMed: 30661993 DOI: 10.1016/j.stemcr.2018.12.012Associated cell lines:
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Majolo F, Marinowic DR, Machado DC, Da Costa JC
Important advances in Alzheimer's disease from the use of induced pluripotent stem cells
Majolo F et al. Important advances in Alzheimer's disease from the use of induced pluripotent stem cells. . 2019-02-06. Pubmed ID: 30728025; DOI: 10.1186/s12929-019-0501-5; PMC: PMC6366077 ASUi001-AASUi002-AASUi003-AASUi004-AZZUi010-A 2019-02-06 2019-02-06 PubMed: 30728025 DOI: 10.1186/s12929-019-0501-5 -
Rajaei S, Fatahi Y, Dabbagh A
Meeting Between Rumi and Shams in Notch Signaling; Implications for Pain Management: A Narrative Review
Rajaei S et al. Meeting Between Rumi and Shams in Notch Signaling; Implications for Pain Management: A Narrative Review. . 2019-02-00. Pubmed ID: 30881911; DOI: 10.5812/aapm.85279; PMC: PMC6412915 CSCRMi001-A 2019-02-00 2019-02-00 PubMed: 30881911 DOI: 10.5812/aapm.85279Associated cell lines:
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Giulitti S, Pellegrini M, Zorzan I, Martini P, Gagliano O, Mutarelli M, Ziller MJ, Cacchiarelli D, Romualdi C, Elvassore N, Martello G
Direct generation of human naive induced pluripotent stem cells from somatic cells in microfluidics
Giulitti S et al. Direct generation of human naive induced pluripotent stem cells from somatic cells in microfluidics. . 2019-02-00. Pubmed ID: 30598530; DOI: 10.1038/s41556-018-0254-5 UNIPDi004-AUNIPDi004-BUNIPDi005-A 2019-02-00 2019-02-00 PubMed: 30598530 DOI: 10.1038/s41556-018-0254-5Associated cell lines:
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Chen Y, Dolt KS, Kriek M, Baker T, Downey P, Drummond NJ, Canham MA, Natalwala A, Rosser S, Kunath T
Engineering synucleinopathy-resistant human dopaminergic neurons by CRISPR-mediated deletion of the SNCA gene
Chen Y et al. Engineering synucleinopathy-resistant human dopaminergic neurons by CRISPR-mediated deletion of the SNCA gene. . 2019-02-00. Pubmed ID: 30472757; DOI: 10.1111/ejn.14286; PMC: PMC6492083 RCe021-AEDi001-B-1EDi001-B-2EDi001-B-3EDi001-B-4 2019-02-00 2019-02-00 PubMed: 30472757 DOI: 10.1111/ejn.14286Associated cell lines:
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Min YL, Bassel-Duby R, Olson EN
CRISPR Correction of Duchenne Muscular Dystrophy
Min YL et al. CRISPR Correction of Duchenne Muscular Dystrophy. . 2019-01-27. Pubmed ID: 30379597; DOI: 10.1146/annurev-med-081117-010451; PMC: PMC6415693 CSCRMi001-A 2019-01-27 2019-01-27 PubMed: 30379597 DOI: 10.1146/annurev-med-081117-010451Associated cell lines:
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Jelinkova S, Fojtik P, Kohutova A, Vilotic A, Marková L, Pesl M, Jurakova T, Kruta M, Vrbsky J, Gaillyova R, Valášková I, Frák I, Lacampagne A, Forte G, Dvorak P, Meli AC, Rotrekl V
Dystrophin Deficiency Leads to Genomic Instability in Human Pluripotent Stem Cells via NO Synthase-Induced Oxidative Stress
Jelinkova S et al. Dystrophin Deficiency Leads to Genomic Instability in Human Pluripotent Stem Cells via NO Synthase-Induced Oxidative Stress. . 2019-01-15. Pubmed ID: 30650618; DOI: 10.3390/cells8010053; PMC: PMC6356905 MUNIe005-AMUNIe007-AMUNIi001-AMUNIi003-A 2019-01-15 2019-01-15 PubMed: 30650618 DOI: 10.3390/cells8010053Associated cell lines:
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Lang C, Campbell KR, Ryan BJ, Carling P, Attar M, Vowles J, Perestenko OV, Bowden R, Baig F, Kasten M, Hu MT, Cowley SA, Webber C, Wade-Martins R
Single-Cell Sequencing of iPSC-Dopamine Neurons Reconstructs Disease Progression and Identifies HDAC4 as a Regulator of Parkinson Cell Phenotypes
Lang C et al. Single-Cell Sequencing of iPSC-Dopamine Neurons Reconstructs Disease Progression and Identifies HDAC4 as a Regulator of Parkinson Cell Phenotypes. . 2019-01-03. Pubmed ID: 30503143; DOI: 10.1016/j.stem.2018.10.023; PMC: PMC6327112 UOXFi001-BUOXFi002-AUOXFi003-AUOXFi004-AUOXFi004-BUOXFi005-AUOXFi005-BSTBCi025-ASTBCi025-BSTBCi043-BSTBCi026-DSTBCi044-BSTBCi101-ASTBCi105-ASTBCi268-ASTBCi294-ASTBCi298-A 2019-01-03 2019-01-03 PubMed: 30503143 DOI: 10.1016/j.stem.2018.10.023 -
Ma L.J.
Induced pluripotent stem cell transplantation for systemic lupus erythematosus in a mouse model
Ma L.J.. Induced pluripotent stem cell transplantation for systemic lupus erythematosus in a mouse model. . 2019-01-01. DOI: 10.3969/j.issn.2095-4344.1826 IMGTi003-A 2019-01-01 2019-01-01 DOI: 10.3969/j.issn.2095-4344.1826Associated cell lines:
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Vlahos K, Sourris K, Mayberry R, McDonald P, Bruveris FF, Schiesser JV, Bozaoglu K, Lockhart PJ, Stanley EG, Elefanty AG
Generation of iPSC lines from peripheral blood mononuclear cells from 5 healthy adults
Vlahos K et al. Generation of iPSC lines from peripheral blood mononuclear cells from 5 healthy adults. . 2019-01-00. Pubmed ID: 30605840; DOI: 10.1016/j.scr.2018.101380 MCRIi001-AMCRIi004-AMCRIi005-AMCRIi006-AMCRIi010-A 2019-01-00 2019-01-00 PubMed: 30605840 DOI: 10.1016/j.scr.2018.101380Associated cell lines:
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Niki T, Imamura K, Enami T, Kinoshita M, Inoue H
Establishment of human induced pluripotent stem cell line from a patient with Angelman syndrome carrying the deletion of maternal chromosome 15q11.2-q13
Niki T et al. Establishment of human induced pluripotent stem cell line from a patient with Angelman syndrome carrying the deletion of maternal chromosome 15q11.2-q13. . 2019-01-00. Pubmed ID: 30605843; DOI: 10.1016/j.scr.2018.101363 CIRAi004-A 2019-01-00 2019-01-00 PubMed: 30605843 DOI: 10.1016/j.scr.2018.101363Associated cell lines:
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Schöndorf DC, Elschami M, Schieck M, Ercan-Herbst E, Weber C, Riesinger Y, Kalman S, Steinemann D, Ehrnhoefer DE
Generation of an induced pluripotent stem cell cohort suitable to investigate sporadic Alzheimer's Disease
Schöndorf DC et al. Generation of an induced pluripotent stem cell cohort suitable to investigate sporadic Alzheimer's Disease. . 2019-01-00. Pubmed ID: 30611016; DOI: 10.1016/j.scr.2018.11.012 BIOMEDi001-ABIOMEDi002-ABIOMEDi004-ABIOMEDi005-ABIOMEDi006-A 2019-01-00 2019-01-00 PubMed: 30611016 DOI: 10.1016/j.scr.2018.11.012Associated cell lines:
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Auboyer L, Monzo C, Wallon D, Rovelet-Lecrux A, Gabelle A, Gazagne I, Cacheux V, Lehmann S, Crozet C
Generation of induced pluripotent stem cells (IRMBi001-A) from an Alzheimer's disease patient carrying a G217D mutation in the PSEN1 gene
Auboyer L et al. Generation of induced pluripotent stem cells (IRMBi001-A) from an Alzheimer's disease patient carrying a G217D mutation in the PSEN1 gene. . 2019-01-00. Pubmed ID: 30677723; DOI: 10.1016/j.scr.2018.101381 IRMBi001-A 2019-01-00 2019-01-00 PubMed: 30677723 DOI: 10.1016/j.scr.2018.101381Associated cell lines:
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Khabarova AA, Pristyazhnyuk IE, Nikitina TV, Gayner TA, Torkhova NB, Skryabin NA, Kashevarova AA, Babushkina NP, Markova ZG, Minzhenkova ME, Nazarenko LP, Shilova NV, Shorina AR, Lebedev IN, Serov OL
Induced pluripotent stem cell line, ICAGi001-A, derived from human skin fibroblasts of a patient with 2p25.3 deletion and 2p25.3-p23.3 inverted duplication
Khabarova AA et al. Induced pluripotent stem cell line, ICAGi001-A, derived from human skin fibroblasts of a patient with 2p25.3 deletion and 2p25.3-p23.3 inverted duplication. . 2019-01-00. Pubmed ID: 30616144; DOI: 10.1016/j.scr.2018.101377 ICGi016-A 2019-01-00 2019-01-00 PubMed: 30616144 DOI: 10.1016/j.scr.2018.101377Associated cell lines:
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Daoutsali E, Buijsen RAM, van de Pas S, Jong A', Mikkers H, Brands T, Eussen B, de Klein A, van der Graaf LM, Pepers BA, Freund C, Terwindt GM, Orlova VV, van Roon-Mom WMC
Generation of 3 human induced pluripotent stem cell lines LUMCi005-A, B and C from a Hereditary Cerebral Hemorrhage with Amyloidosis-Dutch type patient
Daoutsali E et al. Generation of 3 human induced pluripotent stem cell lines LUMCi005-A, B and C from a Hereditary Cerebral Hemorrhage with Amyloidosis-Dutch type patient. . 2019-01-00. Pubmed ID: 30611017; DOI: 10.1016/j.scr.2018.101359 LUMCi005-ALUMCi005-BLUMCi005-C 2019-01-00 2019-01-00 PubMed: 30611017 DOI: 10.1016/j.scr.2018.101359Associated cell lines:
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Lu YQ, Dong EL, Yang WQ, Lai LL, Lin XH, Ma LX, Chen WJ, Wang N, Lin X
Generation of an integration-free induced pluripotent stem cell line, FJMUi001-A, from a hereditary spastic paraplegia patient carrying compound heterozygous p.P498L and p.R618W mutations in CAPN1 (SPG76)
Lu YQ et al. Generation of an integration-free induced pluripotent stem cell line, FJMUi001-A, from a hereditary spastic paraplegia patient carrying compound heterozygous p.P498L and p.R618W mutations in CAPN1 (SPG76). . 2019-01-00. Pubmed ID: 30611022; DOI: 10.1016/j.scr.2018.11.015 FJMUi001-A 2019-01-00 2019-01-00 PubMed: 30611022 DOI: 10.1016/j.scr.2018.11.015Associated cell lines:
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Schmid B, Prehn KR, Nimsanor N, Garcia BIA, Poulsen U, Jørring I, Rasmussen MA, Clausen C, Mau-Holzmann UA, Ramakrishna S, Muddashetty R, Steeg R, Bruce K, Mackintosh P, Ebneth A, Holst B, Cabrera-Socorro A
Generation of a set of isogenic, gene-edited iPSC lines homozygous for all main APOE variants and an APOE knock-out line
Schmid B et al. Generation of a set of isogenic, gene-edited iPSC lines homozygous for all main APOE variants and an APOE knock-out line. . 2019-01-00. Pubmed ID: 30660866; DOI: 10.1016/j.scr.2018.11.010 BIONi010-CBIONi010-C-2BIONi010-C-3BIONi010-C-4BIONi010-C-6 2019-01-00 2019-01-00 PubMed: 30660866 DOI: 10.1016/j.scr.2018.11.010Associated cell lines:
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Wang Y, Sun H, Yang J, Shi C, Liu Y, Xu Y, Zhang J
Generation of induced pluripotent stem cell line (ZZUi0013-A) from a 65-year-old patient with a novel MEOX2 gene mutation in Alzheimer's disease
Wang Y et al. Generation of induced pluripotent stem cell line (ZZUi0013-A) from a 65-year-old patient with a novel MEOX2 gene mutation in Alzheimer's disease. . 2019-01-00. Pubmed ID: 30616143; DOI: 10.1016/j.scr.2018.101366 ZZUi013-A 2019-01-00 2019-01-00 PubMed: 30616143 DOI: 10.1016/j.scr.2018.101366Associated cell lines:
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Ávila-González D, Martínez-Alarcón O, García-López G, Díaz-Martínez NE, Razo-Aguilera G, Valdespino-Vázquez MY, Moreno-Verduzco ER, Vega-Hernández E, Regalado-Hernández JC, De la Jara-Díaz JF, Molina-Hernández A, Flores-Herrera H, Portillo W, Díaz NF
Establishment of human embryonic stem cell line Amicqui-2 using poor-quality embryos from Mexican population
Ávila-González D et al. Establishment of human embryonic stem cell line Amicqui-2 using poor-quality embryos from Mexican population. . 2019-01-00. Pubmed ID: 30611019; DOI: 10.1016/j.scr.2018.101364 INPERe002-A 2019-01-00 2019-01-00 PubMed: 30611019 DOI: 10.1016/j.scr.2018.101364Associated cell lines:
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Bai X, Yang X, Cheng Y, Chen L
Establishment of an induced pluripotent stem cell line (FDEENTi001-A) from a patient with pathological myopia
Bai X et al. Establishment of an induced pluripotent stem cell line (FDEENTi001-A) from a patient with pathological myopia. . 2019-01-00. Pubmed ID: 30611020; DOI: 10.1016/j.scr.2018.101369; PMC: PMC6441353 FDEENTi001-A 2019-01-00 2019-01-00 PubMed: 30611020 DOI: 10.1016/j.scr.2018.101369Associated cell lines:
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Maguire JA, Gagne AL, Gonzalez-Alegre P, Davidson BL, Shakkottai V, Gadue P, French DL
Generation of Spinocerebellar Ataxia Type 2 induced pluripotent stem cell lines, CHOPi002-A and CHOPi003-A, from patients with abnormal CAG repeats in the coding region of the ATXN2 gene
Maguire JA et al. Generation of Spinocerebellar Ataxia Type 2 induced pluripotent stem cell lines, CHOPi002-A and CHOPi003-A, from patients with abnormal CAG repeats in the coding region of the ATXN2 gene. . 2019-01-00. Pubmed ID: 30611021; DOI: 10.1016/j.scr.2018.101361 CHOPi002-ACHOPi003-A 2019-01-00 2019-01-00 PubMed: 30611021 DOI: 10.1016/j.scr.2018.101361Associated cell lines:
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Gustavsson N, Marote A, Pomeshchik Y, Russ K, Azevedo C, Chumarina M, Goldwurm S, Collin A, Pinto L, Salgado AJ, Klementieva O, Roybon L, Savchenko E
Generation of an induced pluripotent stem cell line (CSC-46) from a patient with Parkinson's disease carrying a novel p.R301C mutation in the GBA gene
Gustavsson N et al. Generation of an induced pluripotent stem cell line (CSC-46) from a patient with Parkinson's disease carrying a novel p.R301C mutation in the GBA gene. . 2019-01-00. Pubmed ID: 30640063; DOI: 10.1016/j.scr.2018.101373 ULUNDi007-A 2019-01-00 2019-01-00 PubMed: 30640063 DOI: 10.1016/j.scr.2018.101373Associated cell lines:
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Artero Castro A, Long K, Bassett A, Machuca C, León M, Ávila-Fernandez A, Cortón M, Vidal-Puig T, Ayuso C, Lukovic D, Erceg S
Generation of gene-corrected human induced pluripotent stem cell lines derived from retinitis pigmentosa patient with Ser331Cysfs*5 mutation in MERTK
Artero Castro A et al. Generation of gene-corrected human induced pluripotent stem cell lines derived from retinitis pigmentosa patient with Ser331Cysfs*5 mutation in MERTK. . 2019-01-00. Pubmed ID: 30612079; DOI: 10.1016/j.scr.2018.11.003 RCPFi003-ARCPFi003-A-1RCPFi003-A-2 2019-01-00 2019-01-00 PubMed: 30612079 DOI: 10.1016/j.scr.2018.11.003Associated cell lines:
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Valetdinova KR, Maretina MA, Kuranova ML, Grigor'eva EV, Minina YM, Kizilova EA, Kiselev AV, Medvedev SP, Baranov VS, Zakian SM
Generation of two spinal muscular atrophy (SMA) type I patient-derived induced pluripotent stem cell (iPSC) lines and two SMA type II patient-derived iPSC lines
Valetdinova KR et al. Generation of two spinal muscular atrophy (SMA) type I patient-derived induced pluripotent stem cell (iPSC) lines and two SMA type II patient-derived iPSC lines. . 2019-01-00. Pubmed ID: 30660867; DOI: 10.1016/j.scr.2018.101376 ICGi005-AICGi005-BICGi006-AICGi006-B 2019-01-00 2019-01-00 PubMed: 30660867 DOI: 10.1016/j.scr.2018.101376 -
Li R, Pradhan M, Xu M, Baskfield A, Farkhondeh A, Cheng YS, Beers J, Zou J, Liu C, Might M, Rodems S, Zheng W
Generation of an induced pluripotent stem cell line (TRNDi002-B) from a patient carrying compound heterozygous p.Q208X and p.G310G mutations in the NGLY1 gene
Li R et al. Generation of an induced pluripotent stem cell line (TRNDi002-B) from a patient carrying compound heterozygous p.Q208X and p.G310G mutations in the NGLY1 gene. . 2019-01-00. Pubmed ID: 30612078; DOI: 10.1016/j.scr.2018.101362; PMC: PMC6492929 TRNDi002-B 2019-01-00 2019-01-00 PubMed: 30612078 DOI: 10.1016/j.scr.2018.101362Associated cell lines:
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Li R, Baskfield A, Lin Y, Beers J, Zou J, Liu C, Jaffré F, Roberts AE, Ottinger EA, Kontaridis MI, Zheng W
Generation of an induced pluripotent stem cell line (TRNDi003-A) from a Noonan syndrome with multiple lentigines (NSML) patient carrying a p.Q510P mutation in the PTPN11 gene
Li R et al. Generation of an induced pluripotent stem cell line (TRNDi003-A) from a Noonan syndrome with multiple lentigines (NSML) patient carrying a p.Q510P mutation in the PTPN11 gene. . 2019-01-00. Pubmed ID: 30640061; DOI: 10.1016/j.scr.2018.101374; PMC: PMC7017387 TRNDi003-A 2019-01-00 2019-01-00 PubMed: 30640061 DOI: 10.1016/j.scr.2018.101374Associated cell lines:
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Potirat P, Wattanapanitch M, Viprakasit V, Kheolamai P, Issaragrisil S
An integration-free iPSC line (MUSIi008-A) derived from a patient with severe hemolytic anemia carrying compound heterozygote mutations in KLF1 gene for disease modeling
Potirat P et al. An integration-free iPSC line (MUSIi008-A) derived from a patient with severe hemolytic anemia carrying compound heterozygote mutations in KLF1 gene for disease modeling. . 2019-01-00. Pubmed ID: 30605837; DOI: 10.1016/j.scr.2018.09.021 MUSIi008-A 2019-01-00 2019-01-00 PubMed: 30605837 DOI: 10.1016/j.scr.2018.09.021Associated cell lines:
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Martins S, Bohndorf M, Graffmann N, Wruck W, Chrzanowska KH, Adjaye J
Fibroblast-derived integration-free iPSC line ISRM-NBS1 from an 18-year-old Nijmegen Breakage Syndrome patient carrying the homozygous NBN c.657_661del5 mutation
Martins S et al. Fibroblast-derived integration-free iPSC line ISRM-NBS1 from an 18-year-old Nijmegen Breakage Syndrome patient carrying the homozygous NBN c.657_661del5 mutation. . 2019-01-00. Pubmed ID: 30616142; DOI: 10.1016/j.scr.2018.101372 HHUUKDi006-A 2019-01-00 2019-01-00 PubMed: 30616142 DOI: 10.1016/j.scr.2018.101372Associated cell lines:
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Frederiksen HR, Holst B, Ramakrishna S, Muddashetty R, Schmid B, Freude K
Generation of two iPSC lines with either a heterozygous V717I or a heterozygous KM670/671NL mutation in the APP gene
Frederiksen HR et al. Generation of two iPSC lines with either a heterozygous V717I or a heterozygous KM670/671NL mutation in the APP gene. . 2019-01-00. Pubmed ID: 30634129; DOI: 10.1016/j.scr.2018.101368 BIONi010-C-29BIONi010-C-30BIONi010-C-37BIONi010-C-38 2019-01-00 2019-01-00 PubMed: 30634129 DOI: 10.1016/j.scr.2018.101368Associated cell lines:
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Claassen JN, Zhang D, Chen SC, Moon SY, Lamey T, Thompson JA, McLaren T, De Roach JN, McLenachan S, Chen FK
Generation of the induced pluripotent stem cell line from a patient with autosomal recessive ABCA4-mediated Stargardt Macular Dystrophy
Claassen JN et al. Generation of the induced pluripotent stem cell line from a patient with autosomal recessive ABCA4-mediated Stargardt Macular Dystrophy. . 2019-01-00. Pubmed ID: 30634128; DOI: 10.1016/j.scr.2018.11.013 LEIi007-A 2019-01-00 2019-01-00 PubMed: 30634128 DOI: 10.1016/j.scr.2018.11.013Associated cell lines:
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Tong J, Lee KM, Liu X, Nefzger CM, Vijayakumar P, Hawi Z, Pang KC, Parish CL, Polo JM, Bellgrove MA
Generation of four iPSC lines from peripheral blood mononuclear cells (PBMCs) of an attention deficit hyperactivity disorder (ADHD) individual and a healthy sibling in an Australia-Caucasian family
Tong J et al. Generation of four iPSC lines from peripheral blood mononuclear cells (PBMCs) of an attention deficit hyperactivity disorder (ADHD) individual and a healthy sibling in an Australia-Caucasian family. . 2019-01-00. Pubmed ID: 30622032; DOI: 10.1016/j.scr.2018.11.014 MICCNi001-AMICCNi001-BMICCNi002-AMICCNi002-B 2019-01-00 2019-01-00 PubMed: 30622032 DOI: 10.1016/j.scr.2018.11.014Associated cell lines:
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Marin Navarro A, Day K, Kogner P, Wilhelm M, Falk A
Generation of induced pluripotent stem cell lines from two Neuroblastoma patients carrying a germline ALK R1275Q mutation
Marin Navarro A et al. Generation of induced pluripotent stem cell lines from two Neuroblastoma patients carrying a germline ALK R1275Q mutation. . 2019-01-00. Pubmed ID: 30605844; DOI: 10.1016/j.scr.2018.11.017 KIi001-AKIi002-A 2019-01-00 2019-01-00 PubMed: 30605844 DOI: 10.1016/j.scr.2018.11.017 -
Grigor'eva EV, Malankhanova TB, Surumbayeva A, Minina JM, Morozov VV, Abramycheva NY, Illarioshkin SN, Malakhova AA, Zakian SM
Generation of induced pluripotent stem cell line, ICGi007-A, by reprogramming peripheral blood mononuclear cells from a patient with Huntington's disease
Grigor'eva EV et al. Generation of induced pluripotent stem cell line, ICGi007-A, by reprogramming peripheral blood mononuclear cells from a patient with Huntington's disease. . 2019-01-00. Pubmed ID: 30658253; DOI: 10.1016/j.scr.2018.101382 ICGi007-A 2019-01-00 2019-01-00 PubMed: 30658253 DOI: 10.1016/j.scr.2018.101382Associated cell lines:
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Hariharan K, Stachelscheid H, Rossbach B, Oh SJ, Mah N, Schmidt-Ott K, Kurtz A, Reinke P
Parallel generation of easily selectable multiple nephronal cell types from human pluripotent stem cells
Hariharan K et al. Parallel generation of easily selectable multiple nephronal cell types from human pluripotent stem cells. . 2019-01-00. Pubmed ID: 30310934; DOI: 10.1007/s00018-018-2929-2; PMC: PMC11105784 WAe001-AWISCi004-ABCRTi004-ABCRTi005-A 2019-01-00 2019-01-00 PubMed: 30310934 DOI: 10.1007/s00018-018-2929-2Associated cell lines:
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Najar AH, Sneha KM, Ashok A, Babu S, Subramaniam AG, Kannan R, Viswanath B, Purushottam M, Varghese M, Parvez S, Panicker MM, Mukherjee O, Jain S
Derivation of iPSC lines from two patients with familial Alzheimer's disease from India
Najar AH et al. Derivation of iPSC lines from two patients with familial Alzheimer's disease from India. . 2019-01-00. Pubmed ID: 30605839; DOI: 10.1016/j.scr.2018.101370 NCBSi001-ANCBSi002-A 2019-01-00 2019-01-00 PubMed: 30605839 DOI: 10.1016/j.scr.2018.101370Associated cell lines:
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Peng CH, Huang KC, Lu HE, Syu SH, Yarmishyn AA, Lu JF, Buddhakosai W, Lin TC, Hsu CC, Hwang DK, Shen CN, Chen SJ, Chiou SH
Corrigendum to "Generation of induced pluripotent stem cells from a patient with X-linked juvenile retinoschisis" [Stem Cell Res. 29(2018): 152-156]
Peng CH et al. Corrigendum to "Generation of induced pluripotent stem cells from a patient with X-linked juvenile retinoschisis" [Stem Cell Res. 29(2018): 152-156]. . 2019-01-00. Pubmed ID: 30736915; DOI: 10.1016/j.scr.2019.101388 TVGHi003-A 2019-01-00 2019-01-00 PubMed: 30736915 DOI: 10.1016/j.scr.2019.101388Associated cell lines:
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Yin Y, Petersen AJ, Soref C, Richards WD, Ludwig T, Taapken S, Berndt E, Zhang SC, Bhattacharyya A
Generation of seven induced pluripotent stem cell lines from neonates of different ethnic backgrounds
Yin Y et al. Generation of seven induced pluripotent stem cell lines from neonates of different ethnic backgrounds. . 2019-01-00. Pubmed ID: 30605841; DOI: 10.1016/j.scr.2018.101365; PMC: PMC7086470 WISCi007-AWISCi007-BWISCi007-CWISCi008-AWISCi008-BWISCi008-CWISCi009-A 2019-01-00 2019-01-00 PubMed: 30605841 DOI: 10.1016/j.scr.2018.101365Associated cell lines:
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Schuster S, Saravanakumar S, Schöls L, Hauser S
Generation of a homozygous CRISPR/Cas9-mediated knockout human iPSC line for the STUB1 locus
Schuster S et al. Generation of a homozygous CRISPR/Cas9-mediated knockout human iPSC line for the STUB1 locus. . 2019-01-00. Pubmed ID: 30605842; DOI: 10.1016/j.scr.2018.101378 HIHCNi004-AHIHCNi004-A-1 2019-01-00 2019-01-00 PubMed: 30605842 DOI: 10.1016/j.scr.2018.101378Associated cell lines:
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McLenachan S, Zhang D, Zhang X, Chen SC, Lamey T, Thompson JA, McLaren T, De Roach JN, Fletcher S, Chen FK
Generation of two induced pluripotent stem cell lines from a patient with dominant PRPF31 mutation and a related non-penetrant carrier
McLenachan S et al. Generation of two induced pluripotent stem cell lines from a patient with dominant PRPF31 mutation and a related non-penetrant carrier. . 2019-01-00. Pubmed ID: 30611018; DOI: 10.1016/j.scr.2018.11.018 LEIi008-ALEIi009-A 2019-01-00 2019-01-00 PubMed: 30611018 DOI: 10.1016/j.scr.2018.11.018 -
Li Y, Huang C, Zha L, Kong M, Yang Q, Zhu Y, Peng Y, Ouyang Q, Lu G, Lin G, Zhou D
Generation of NERCe003-A-3, a p53 compound heterozygous mutation human embryonic stem cell line, by CRISPR/Cas9 editing
Li Y et al. Generation of NERCe003-A-3, a p53 compound heterozygous mutation human embryonic stem cell line, by CRISPR/Cas9 editing. . 2019-01-00. Pubmed ID: 30658254; DOI: 10.1016/j.scr.2018.101371 NERCe003-ANERCe003-A-3 2019-01-00 2019-01-00 PubMed: 30658254 DOI: 10.1016/j.scr.2018.101371Associated cell lines:
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Huo Z, Tu J, Xu A, Li Y, Wang D, Liu M, Zhou R, Zhu D, Lin Y, Gingold JA, Yen CJ, Xiao H, Zhao R
Generation of a heterozygous p53 R249S mutant human embryonic stem cell line by TALEN-mediated genome editing
Huo Z et al. Generation of a heterozygous p53 R249S mutant human embryonic stem cell line by TALEN-mediated genome editing. . 2019-01-00. Pubmed ID: 30640060; DOI: 10.1016/j.scr.2018.101360 WAe009-A-11 2019-01-00 2019-01-00 PubMed: 30640060 DOI: 10.1016/j.scr.2018.101360Associated cell lines:
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Namer B, Schmidt D, Eberhardt E, Maroni M, Dorfmeister E, Kleggetveit IP, Kaluza L, Meents J, Gerlach A, Lin Z, Winterpacht A, Dragicevic E, Kohl Z, Schüttler J, Kurth I, Warncke T, Jorum E, Winner B, Lampert A
Pain relief in a neuropathy patient by lacosamide: Proof of principle of clinical translation from patient-specific iPS cell-derived nociceptors
Namer B et al. Pain relief in a neuropathy patient by lacosamide: Proof of principle of clinical translation from patient-specific iPS cell-derived nociceptors. . 2019-01-00. Pubmed ID: 30503201; DOI: 10.1016/j.ebiom.2018.11.042; PMC: PMC6354557 UKERi005-AUKERi006-B 2019-01-00 2019-01-00 PubMed: 30503201 DOI: 10.1016/j.ebiom.2018.11.042Associated cell lines:
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Xue Y, Liao B, Xie Y, Li S, Ma X, Sun X
Establishment of an ectodermal dysplasia related gene EDA Knockout human embryonic stem cell line (WAe001-A-22) by CRISPR-Cas9 technology
Xue Y et al. Establishment of an ectodermal dysplasia related gene EDA Knockout human embryonic stem cell line (WAe001-A-22) by CRISPR-Cas9 technology. . 2019-01-00. Pubmed ID: 30605838; DOI: 10.1016/j.scr.2018.101379 WAe001-AWAe001-A-22 2019-01-00 2019-01-00 PubMed: 30605838 DOI: 10.1016/j.scr.2018.101379Associated cell lines:
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Danesi C, Achuta VS, Corcoran P, Peteri UK, Turconi G, Matsui N, Albayrak I, Rezov V, Isaksson A, Castrén ML
Increased Calcium Influx through L-type Calcium Channels in Human and Mouse Neural Progenitors Lacking Fragile X Mental Retardation Protein
Danesi C et al. Increased Calcium Influx through L-type Calcium Channels in Human and Mouse Neural Progenitors Lacking Fragile X Mental Retardation Protein. . 2018-12-11. Pubmed ID: 30503263; DOI: 10.1016/j.stemcr.2018.11.003; PMC: PMC6294261 ULBi003-AUHi007-B 2018-12-11 2018-12-11 PubMed: 30503263 DOI: 10.1016/j.stemcr.2018.11.003 -
Lemme M, Ulmer BM, Lemoine MD, Zech ATL, Flenner F, Ravens U, Reichenspurner H, Rol-Garcia M, Smith G, Hansen A, Christ T, Eschenhagen T
Atrial-like Engineered Heart Tissue: An In Vitro Model of the Human Atrium
Lemme M et al. Atrial-like Engineered Heart Tissue: An In Vitro Model of the Human Atrium. . 2018-12-11. Pubmed ID: 30416051; DOI: 10.1016/j.stemcr.2018.10.008; PMC: PMC6294072 UKEi001-A 2018-12-11 2018-12-11 PubMed: 30416051 DOI: 10.1016/j.stemcr.2018.10.008Associated cell lines:
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Echigoya Y, Lim KRQ, Nakamura A, Yokota T
Multiple Exon Skipping in the Duchenne Muscular Dystrophy Hot Spots: Prospects and Challenges
Echigoya Y et al. Multiple Exon Skipping in the Duchenne Muscular Dystrophy Hot Spots: Prospects and Challenges. . 2018-12-07. Pubmed ID: 30544634; DOI: 10.3390/jpm8040041; PMC: PMC6313462 IITi001-A 2018-12-07 2018-12-07 PubMed: 30544634 DOI: 10.3390/jpm8040041Associated cell lines:
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O'Neill AC, Kyrousi C, Klaus J, Leventer RJ, Kirk EP, Fry A, Pilz DT, Morgan T, Jenkins ZA, Drukker M, Berkovic SF, Scheffer IE, Guerrini R, Markie DM, Götz M, Cappello S, Robertson SP
A Primate-Specific Isoform of PLEKHG6 Regulates Neurogenesis and Neuronal Migration
O'Neill AC et al. A Primate-Specific Isoform of PLEKHG6 Regulates Neurogenesis and Neuronal Migration. . 2018-12-04. Pubmed ID: 30517861; DOI: 10.1016/j.celrep.2018.11.029 ISFi001-A 2018-12-04 2018-12-04 PubMed: 30517861 DOI: 10.1016/j.celrep.2018.11.029Associated cell lines:
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Sasaki-Honda M, Jonouchi T, Arai M, Hotta A, Mitsuhashi S, Nishino I, Matsuda R, Sakurai H
A patient-derived iPSC model revealed oxidative stress increases facioscapulohumeral muscular dystrophy-causative DUX4
Sasaki-Honda M et al. A patient-derived iPSC model revealed oxidative stress increases facioscapulohumeral muscular dystrophy-causative DUX4. . 2018-12-01. Pubmed ID: 30107443; DOI: 10.1093/hmg/ddy293; PMC: PMC6240734 CIRAi005-A 2018-12-01 2018-12-01 PubMed: 30107443 DOI: 10.1093/hmg/ddy293Associated cell lines:
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Anderson RH, Kerkvliet JG, Otta JJ, Ross AD, Leiferman PC, Hoppe AD, Francis KR
Generation of a CLTA reporter human induced pluripotent stem cell line, CRMi001-A-1, using the CRISPR/Cas9 system to monitor endogenous clathrin trafficking
Anderson RH et al. Generation of a CLTA reporter human induced pluripotent stem cell line, CRMi001-A-1, using the CRISPR/Cas9 system to monitor endogenous clathrin trafficking. . 2018-12-00. Pubmed ID: 30340091; DOI: 10.1016/j.scr.2018.10.001; PMC: PMC6383648 CRMi001-ACRMi001-A-1 2018-12-00 2018-12-00 PubMed: 30340091 DOI: 10.1016/j.scr.2018.10.001Associated cell lines:
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Wang Y, Fen Q, Yu H, Qiu H, Ma X, Lei Y, Zhao J
Establishment of TUSMi005-A, an induced pluripotent stem cell (iPSC) line from a 32-year old Chinese Han patient with Bipolar Disorder (BD)
Wang Y et al. Establishment of TUSMi005-A, an induced pluripotent stem cell (iPSC) line from a 32-year old Chinese Han patient with Bipolar Disorder (BD). . 2018-12-00. Pubmed ID: 30316949; DOI: 10.1016/j.scr.2018.10.014 TUSMi005-A 2018-12-00 2018-12-00 PubMed: 30316949 DOI: 10.1016/j.scr.2018.10.014Associated cell lines:
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Baulier E, Garcia Diaz A, Corneo B, Farber DB
Generation of a human Ocular Albinism type 1 iPSC line, SEIi001-A, with a mutation in GPR143
Baulier E et al. Generation of a human Ocular Albinism type 1 iPSC line, SEIi001-A, with a mutation in GPR143. . 2018-12-00. Pubmed ID: 30513407; DOI: 10.1016/j.scr.2018.11.016 SEIi001-A 2018-12-00 2018-12-00 PubMed: 30513407 DOI: 10.1016/j.scr.2018.11.016Associated cell lines:
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Neureiter A, Brändl B, Hiber M, Tandon R, Müller FJ, Steenpass L
Generation of an iPSC line of a patient with Angelman syndrome due to an imprinting defect
Neureiter A et al. Generation of an iPSC line of a patient with Angelman syndrome due to an imprinting defect. . 2018-12-00. Pubmed ID: 30296670; DOI: 10.1016/j.scr.2018.09.015 ZIPi015-K 2018-12-00 2018-12-00 PubMed: 30296670 DOI: 10.1016/j.scr.2018.09.015Associated cell lines:
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Sanjurjo-Soriano C, Erkilic N, Manes G, Dubois G, Hamel CP, Meunier I, Kalatzis V
Generation of an iPSC line, INMi001-A, carrying the two most common USH2A mutations from a compound heterozygote with non-syndromic retinitis pigmentosa
Sanjurjo-Soriano C et al. Generation of an iPSC line, INMi001-A, carrying the two most common USH2A mutations from a compound heterozygote with non-syndromic retinitis pigmentosa. . 2018-12-00. Pubmed ID: 30453153; DOI: 10.1016/j.scr.2018.11.004 INMi001-A 2018-12-00 2018-12-00 PubMed: 30453153 DOI: 10.1016/j.scr.2018.11.004Associated cell lines:
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Tandon R, Brändl B, Baryshnikova N, Landshammer A, Steenpaß L, Keminer O, Pless O, Müller FJ
Generation of two human isogenic iPSC lines from fetal dermal fibroblasts
Tandon R et al. Generation of two human isogenic iPSC lines from fetal dermal fibroblasts. . 2018-12-00. Pubmed ID: 30343101; DOI: 10.1016/j.scr.2018.10.004 ZIPi013-BZIPi013-E 2018-12-00 2018-12-00 PubMed: 30343101 DOI: 10.1016/j.scr.2018.10.004 -
Erdlenbruch F, Rohwedel J, Ralfs P, Thomitzek A, Kramer J, Cakiroglu F
Generation of induced pluripotent stem cells (iPSCs) from human foreskin fibroblasts
Erdlenbruch F et al. Generation of induced pluripotent stem cells (iPSCs) from human foreskin fibroblasts. . 2018-12-00. Pubmed ID: 30321832; DOI: 10.1016/j.scr.2018.10.010 VUZUZLi001-A 2018-12-00 2018-12-00 PubMed: 30321832 DOI: 10.1016/j.scr.2018.10.010Associated cell lines:
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Huang C, Li Y, Zhao W, Zhang A, Lu C, Wang Z, Liu L
α2δ1 may be a potential marker for cancer stem cell in laryngeal squamous cell carcinoma
Huang C et al. α2δ1 may be a potential marker for cancer stem cell in laryngeal squamous cell carcinoma. . 2019-00-00. Pubmed ID: 30475757; DOI: 10.3233/cbm-181947; PMC: PMC6398553 ISMMSi002-B 2019-00-00 2019-00-00 PubMed: 30475757 DOI: 10.3233/cbm-181947Associated cell lines:
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Wattanapanitch M
Recent Updates on Induced Pluripotent Stem Cells in Hematological Disorders
Wattanapanitch M. Recent Updates on Induced Pluripotent Stem Cells in Hematological Disorders. . 2019-00-00. Pubmed ID: 31191673; DOI: 10.1155/2019/5171032; PMC: PMC6525795 MUSIi005-AMUSIi006-A 2019-00-00 2019-00-00 PubMed: 31191673 DOI: 10.1155/2019/5171032Associated cell lines:
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Nikitina TV, Menzorov AG, Kashevarova AA, Gridina MM, Khabarova AA, Yakovleva YS, Lopatkina ME, Pristyazhnyuk IE, Vasilyev SA, Serov OL, Lebedev IN
Induced pluripotent stem cell line, IMGTi003-A, derived from skin fibroblasts of an intellectually disabled patient with ring chromosome 13
Nikitina TV et al. Induced pluripotent stem cell line, IMGTi003-A, derived from skin fibroblasts of an intellectually disabled patient with ring chromosome 13. . 2018-12-00. Pubmed ID: 30500678; DOI: 10.1016/j.scr.2018.11.009 IMGTi003-A 2018-12-00 2018-12-00 PubMed: 30500678 DOI: 10.1016/j.scr.2018.11.009Associated cell lines:
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Sanjurjo-Soriano C, Erkilic N, Manes G, Dubois G, Hamel CP, Meunier I, Kalatzis V
Generation of a human iPSC line, INMi002-A, carrying the most prevalent USH2A variant associated with Usher syndrome type 2
Sanjurjo-Soriano C et al. Generation of a human iPSC line, INMi002-A, carrying the most prevalent USH2A variant associated with Usher syndrome type 2. . 2018-12-00. Pubmed ID: 30468996; DOI: 10.1016/j.scr.2018.11.007 INMi002-A 2018-12-00 2018-12-00 PubMed: 30468996 DOI: 10.1016/j.scr.2018.11.007Associated cell lines:
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Angelini C, Pinzan E
Advances in imaging of brain abnormalities in neuromuscular disease
Angelini C et al. Advances in imaging of brain abnormalities in neuromuscular disease. . 2019-00-00. Pubmed ID: 31105770; DOI: 10.1177/1756286419845567; PMC: PMC6503605 CSCRMi001-A 2019-00-00 2019-00-00 PubMed: 31105770 DOI: 10.1177/1756286419845567Associated cell lines:
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Ahmed E, Sansac C, Fieldes M, Bergougnoux A, Bourguignon C, Mianné J, Arnould C, Vachier I, Assou S, Bourdin A, De Vos J
Generation of the induced pluripotent stem cell line UHOMi001-A from a patient with mutations in CCDC40 gene causing Primary Ciliary Dyskinesia (PCD)
Ahmed E et al. Generation of the induced pluripotent stem cell line UHOMi001-A from a patient with mutations in CCDC40 gene causing Primary Ciliary Dyskinesia (PCD). . 2018-12-00. Pubmed ID: 30296669; DOI: 10.1016/j.scr.2018.09.019 UHOMi001-A 2018-12-00 2018-12-00 PubMed: 30296669 DOI: 10.1016/j.scr.2018.09.019Associated cell lines:
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Schipper L, Kanber D, Steenpass L
Generation of heterozygous and homozygous hESC H9 sublines carrying inactivating mutations in RB1
Schipper L et al. Generation of heterozygous and homozygous hESC H9 sublines carrying inactivating mutations in RB1. . 2018-12-00. Pubmed ID: 30312872; DOI: 10.1016/j.scr.2018.09.016 WAe009-AWAe009-A-12WAe009-A-13 2018-12-00 2018-12-00 PubMed: 30312872 DOI: 10.1016/j.scr.2018.09.016Associated cell lines:
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Fernández-Susavila H, Bugallo-Casal A, Castillo J, Campos F
Adult Stem Cells and Induced Pluripotent Stem Cells for Stroke Treatment
Fernández-Susavila H et al. Adult Stem Cells and Induced Pluripotent Stem Cells for Stroke Treatment. . 2019-00-00. Pubmed ID: 31555195; DOI: 10.3389/fneur.2019.00908; PMC: PMC6722184 IDISi001-A 2019-00-00 2019-00-00 PubMed: 31555195 DOI: 10.3389/fneur.2019.00908Associated cell lines:
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Wang Y, Zhang J, Lei Y, Zhao J
Establishment of TUSMi007-A, an induced pluripotent stem cell (iPSC) line from an 83-year old Chinese Han patient with Alzheimer's disease (AD)
Wang Y et al. Establishment of TUSMi007-A, an induced pluripotent stem cell (iPSC) line from an 83-year old Chinese Han patient with Alzheimer's disease (AD). . 2018-12-00. Pubmed ID: 30503970; DOI: 10.1016/j.scr.2018.11.008 TUSMi007-A 2018-12-00 2018-12-00 PubMed: 30503970 DOI: 10.1016/j.scr.2018.11.008Associated cell lines:
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Chan YH, Cheng YF, Chen YT, Huang CY, Lin CH, Hu CJ, Lu YC, Wu CC, Hsu CJ
Generation of induced pluripotent stem cells from a patient with hearing loss carrying GJB2 p.V37I mutation
Chan YH et al. Generation of induced pluripotent stem cells from a patient with hearing loss carrying GJB2 p.V37I mutation. . 2018-12-00. Pubmed ID: 30316039; DOI: 10.1016/j.scr.2018.10.002 IBMSi010-A 2018-12-00 2018-12-00 PubMed: 30316039 DOI: 10.1016/j.scr.2018.10.002Associated cell lines:
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Zhao Z, Ji S, Shi Z, Liu H
Generation of CSi001-A, a transgene-free, induced pluripotent stem cell line derived from a Parkinson Disease (PD) patient
Zhao Z et al. Generation of CSi001-A, a transgene-free, induced pluripotent stem cell line derived from a Parkinson Disease (PD) patient. . 2018-12-00. Pubmed ID: 30292881; DOI: 10.1016/j.scr.2018.09.020 CSi001-A 2018-12-00 2018-12-00 PubMed: 30292881 DOI: 10.1016/j.scr.2018.09.020Associated cell lines:
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Srivastava AchalK, Kumar Deepak, Faruq Mohammad, Gundluru VarunR
Spinocerebellar ataxia type 12: An update
Srivastava AchalK et al. Spinocerebellar ataxia type 12: An update. . 2019-00-00. DOI: 10.4103/aomd.aomd_5_19 IGIBi002-AIGIBi003-AIGIBi004-A 2019-00-00 2019-00-00 DOI: 10.4103/aomd.aomd_5_19Associated cell lines:
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Golgooni Zeinab, Mirsadeghi Sara, Soleymani Baghshah Mahdieh, Ataee Pedram, Baharvand Hossein, Pahlavan Sara, Rabiee Hamid R.
Deep Learning-Based Proarrhythmia Analysis Using Field Potentials Recorded From Human Pluripotent Stem Cells Derived Cardiomyocytes
Golgooni Zeinab et al. Deep Learning-Based Proarrhythmia Analysis Using Field Potentials Recorded From Human Pluripotent Stem Cells Derived Cardiomyocytes. . 2019-00-00. DOI: 10.1109/jtehm.2019.2907945 UKKi007-AUKKi009-A 2019-00-00 2019-00-00 DOI: 10.1109/jtehm.2019.2907945 -
Schwarz N, Uysal B, Rosa F, Löffler H, Mau-Holzmann UA, Liebau S, Lerche H
Generation of an induced pluripotent stem cell (iPSC) line from a patient with developmental and epileptic encephalopathy carrying a KCNA2 (p.Leu328Val) mutation
Schwarz N et al. Generation of an induced pluripotent stem cell (iPSC) line from a patient with developmental and epileptic encephalopathy carrying a KCNA2 (p.Leu328Val) mutation. . 2018-12-00. Pubmed ID: 30292882; DOI: 10.1016/j.scr.2018.08.019 HIHDNEi001-A 2018-12-00 2018-12-00 PubMed: 30292882 DOI: 10.1016/j.scr.2018.08.019Associated cell lines:
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Klein T, Henkel L, Klug K, Kwok CK, Klopocki E, Üçeyler N
Generation of the human induced pluripotent stem cell line UKWNLi002-A from dermal fibroblasts of a woman with a heterozygous c.608 C>T (p.Thr203Met) mutation in exon 3 of the nerve growth factor gene potentially associated with hereditary sensory and autonomic neuropathy type 5
Klein T et al. Generation of the human induced pluripotent stem cell line UKWNLi002-A from dermal fibroblasts of a woman with a heterozygous c.608 C>T (p.Thr203Met) mutation in exon 3 of the nerve growth factor gene potentially associated with hereditary sensory and autonomic neuropathy type 5. . 2018-12-00. Pubmed ID: 30384131; DOI: 10.1016/j.scr.2018.10.017 UKWNLi002-A 2018-12-00 2018-12-00 PubMed: 30384131 DOI: 10.1016/j.scr.2018.10.017Associated cell lines:
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Calado SM, Garcia-Delgado AB, De la Cerda B, Ponte-Zuñiga B, Bhattacharya SS, Díaz-Corrales FJ
Generation of a human iPS cell line from a patient with retinitis pigmentosa due to EYS mutation
Calado SM et al. Generation of a human iPS cell line from a patient with retinitis pigmentosa due to EYS mutation. . 2018-12-00. Pubmed ID: 30471616; DOI: 10.1016/j.scr.2018.11.002 CABi002-A 2018-12-00 2018-12-00 PubMed: 30471616 DOI: 10.1016/j.scr.2018.11.002Associated cell lines:
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Tai L, Teoh HK, Cheong SK
Reprogramming human dermal fibroblast into induced pluripotent stem cells using nonintegrative Sendai virus for transduction
Tai L et al. Reprogramming human dermal fibroblast into induced pluripotent stem cells using nonintegrative Sendai virus for transduction. . 2018-12-00. Pubmed ID: 30580364 UTARi001-A 2018-12-00 2018-12-00 PubMed: 30580364Associated cell lines:
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Piga D, Salani S, Magri F, Brusa R, Mauri E, Comi GP, Bresolin N, Corti S
Human induced pluripotent stem cell models for the study and treatment of Duchenne and Becker muscular dystrophies
Piga D et al. Human induced pluripotent stem cell models for the study and treatment of Duchenne and Becker muscular dystrophies. . 2019-00-00. Pubmed ID: 31105767; DOI: 10.1177/1756286419833478; PMC: PMC6501480 IITi001-A 2019-00-00 2019-00-00 PubMed: 31105767 DOI: 10.1177/1756286419833478Associated cell lines:
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Jewell BE, Liu M, Lu L, Zhou R, Tu J, Zhu D, Huo Z, Xu A, Wang D, Mata H, Jin W, Xia W, Rao PH, Zhao R, Hung MC, Wang LL, Lee DF
Generation of an induced pluripotent stem cell line from an individual with a heterozygous RECQL4 mutation
Jewell BE et al. Generation of an induced pluripotent stem cell line from an individual with a heterozygous RECQL4 mutation. . 2018-12-00. Pubmed ID: 30312871; DOI: 10.1016/j.scr.2018.10.003; PMC: PMC6317900 CDMLi002-A 2018-12-00 2018-12-00 PubMed: 30312871 DOI: 10.1016/j.scr.2018.10.003Associated cell lines:
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Baumann H, Jahn M, Muenchau A, Trilck-Winkler M, Lohmann K, Seibler P
Generation and characterization of eight human-derived iPSC lines from affected and unaffected THAP1 mutation carriers
Baumann H et al. Generation and characterization of eight human-derived iPSC lines from affected and unaffected THAP1 mutation carriers. . 2018-12-00. Pubmed ID: 30316041; DOI: 10.1016/j.scr.2018.09.018 LUEi001-ALUEi002-ALUEi002-BLUEi003-ALUEi004-ALUEi004-BLUEi005-ALUEi005-B 2018-12-00 2018-12-00 PubMed: 30316041 DOI: 10.1016/j.scr.2018.09.018 -
Hamad S, Derichsweiler D, Papadopoulos S, Nguemo F, Šarić T, Sachinidis A, Brockmeier K, Hescheler J, Boukens BJ, Pfannkuche K
Generation of human induced pluripotent stem cell-derived cardiomyocytes in 2D monolayer and scalable 3D suspension bioreactor cultures with reduced batch-to-batch variations
Hamad S et al. Generation of human induced pluripotent stem cell-derived cardiomyocytes in 2D monolayer and scalable 3D suspension bioreactor cultures with reduced batch-to-batch variations. . 2019-00-00. Pubmed ID: 31695764; DOI: 10.7150/thno.32058; PMC: PMC6831300 UKKi011-AUKKi032-C 2019-00-00 2019-00-00 PubMed: 31695764 DOI: 10.7150/thno.32058 -
Vallejo-Diez S, Fleischer A, Martín-Fernández JM, Sánchez-Gilabert A, Bachiller D
Generation of two induced pluripotent stem cells lines from a Mucopolysaccharydosis IIIB (MPSIIIB) patient
Vallejo-Diez S et al. Generation of two induced pluripotent stem cells lines from a Mucopolysaccharydosis IIIB (MPSIIIB) patient. . 2018-12-00. Pubmed ID: 30408744; DOI: 10.1016/j.scr.2018.10.019 IMEDEAi005-AIMEDEAi005-B 2018-12-00 2018-12-00 PubMed: 30408744 DOI: 10.1016/j.scr.2018.10.019Associated cell lines:
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Slembrouck-Brec A, Rodrigues A, Rabesandratana O, Gagliardi G, Nanteau C, Fouquet S, Thuret G, Reichman S, Orieux G, Goureau O
Reprogramming of Adult Retinal Müller Glial Cells into Human-Induced Pluripotent Stem Cells as an Efficient Source of Retinal Cells
Slembrouck-Brec A et al. Reprogramming of Adult Retinal Müller Glial Cells into Human-Induced Pluripotent Stem Cells as an Efficient Source of Retinal Cells. . 2019-00-00. Pubmed ID: 31396286; DOI: 10.1155/2019/7858796; PMC: PMC6664555 IDVi005-A 2019-00-00 2019-00-00 PubMed: 31396286 DOI: 10.1155/2019/7858796Associated cell lines:
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Ackermann M, Kempf H, Hetzel M, Hesse C, Hashtchin AR, Brinkert K, Schott JW, Haake K, Kühnel MP, Glage S, Figueiredo C, Jonigk D, Sewald K, Schambach A, Wronski S, Moritz T, Martin U, Zweigerdt R, Munder A, Lachmann N
Bioreactor-based mass production of human iPSC-derived macrophages enables immunotherapies against bacterial airway infections
Ackermann M et al. Bioreactor-based mass production of human iPSC-derived macrophages enables immunotherapies against bacterial airway infections. . 2018-11-30. Pubmed ID: 30504915; DOI: 10.1038/s41467-018-07570-7; PMC: PMC6269475 MHHi015-A 2018-11-30 2018-11-30 PubMed: 30504915 DOI: 10.1038/s41467-018-07570-7Associated cell lines:
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Machuca C, Vilches A, Clemente E, Pascual-Pascual SI, Bolinches-Amorós A, Artero Castro A, Espinos C, Leon M, Jendelova P, Erceg S
Generation of human induced pluripotent stem cell (iPSC) line from an unaffected female carrier of mutation in SACSIN gene
Machuca C et al. Generation of human induced pluripotent stem cell (iPSC) line from an unaffected female carrier of mutation in SACSIN gene. . 2018-12-00. Pubmed ID: 30384130; DOI: 10.1016/j.scr.2018.10.016 ESi043-AESi064-A 2018-12-00 2018-12-00 PubMed: 30384130 DOI: 10.1016/j.scr.2018.10.016 -
Ciampi O, Romano E, Benigni A, Tomasoni S
Generation of two isogenic iPS cell lines (IRFMNi002-A and IRFMNi002-B) from a patient affected by Focal Segmental Glomerulosclerosis carrying a heterozygous c.565G>A mutation in PAX2 gene
Ciampi O et al. Generation of two isogenic iPS cell lines (IRFMNi002-A and IRFMNi002-B) from a patient affected by Focal Segmental Glomerulosclerosis carrying a heterozygous c.565G>A mutation in PAX2 gene. . 2018-12-00. Pubmed ID: 30399566; DOI: 10.1016/j.scr.2018.10.018; PMC: PMC6288238 IRFMNi002-AIRFMNi002-BIRFMNi001-BIRFMNi001-B-1 2018-12-00 2018-12-00 PubMed: 30399566 DOI: 10.1016/j.scr.2018.10.018Associated cell lines:
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Martins GLS, Paredes BD, Azevedo CM, Sampaio GLA, Nonaka CKV, Cavalcante BRR, Da Silva KN, Pereira CSE, Soares MBP, Dos Santos RR, Souza BSF
Generation of integration-free iPS cell lines from three sickle cell disease patients from the state of Bahia, Brazil
Martins GLS et al. Generation of integration-free iPS cell lines from three sickle cell disease patients from the state of Bahia, Brazil. . 2018-12-00. Pubmed ID: 30296668; DOI: 10.1016/j.scr.2018.09.011 CBTCi005-ACBTCi006-ACBTCi007-A 2018-12-00 2018-12-00 PubMed: 30296668 DOI: 10.1016/j.scr.2018.09.011Associated cell lines:
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Kahounová Z, Slabáková E, Binó L, Remšík J, Fedr R, Bouchal J, Kurfűrstová D, Vrtěl R, Študent V, Jurečková L, Porokh V, Hampl A, Souček K
Generation of human iPSCs from human prostate cancer-associated fibroblasts IBPi002-A
Kahounová Z et al. Generation of human iPSCs from human prostate cancer-associated fibroblasts IBPi002-A. . 2018-12-00. Pubmed ID: 30481741; DOI: 10.1016/j.scr.2018.11.006 IBPi002-A 2018-12-00 2018-12-00 PubMed: 30481741 DOI: 10.1016/j.scr.2018.11.006Associated cell lines:
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Avazzadeh S, McDonagh K, Reilly J, Wang Y, Boomkamp SD, McInerney V, Krawczyk J, Fitzgerald J, Feerick N, O'Sullivan M, Jalali A, Forman EB, Lynch SA, Ennis S, Cosemans N, Peeters H, Dockery P, O'Brien T, Quinlan LR, Gallagher L, Shen S
Increased Ca(2+) signaling in NRXN1α(+/-) neurons derived from ASD induced pluripotent stem cells
Avazzadeh S et al. Increased Ca(2+) signaling in NRXN1α(+/-) neurons derived from ASD induced pluripotent stem cells. . 2019-00-00. Pubmed ID: 31893021; DOI: 10.1186/s13229-019-0303-3; PMC: PMC6937972 NUIGi039-ANUIGi045-A 2019-00-00 2019-00-00 PubMed: 31893021 DOI: 10.1186/s13229-019-0303-3Associated cell lines:
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Lukovic D, Artero Castro A, León M, Del Buey Furió V, Cortón M, Ayuso C, Erceg S
Generation of a human iPSC line from a patient with Leber congenital amaurosis caused by mutation in AIPL1
Lukovic D et al. Generation of a human iPSC line from a patient with Leber congenital amaurosis caused by mutation in AIPL1. . 2018-12-00. Pubmed ID: 30366342; DOI: 10.1016/j.scr.2018.10.012 RCPFi007-A 2018-12-00 2018-12-00 PubMed: 30366342 DOI: 10.1016/j.scr.2018.10.012Associated cell lines:
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Pollini D, Loffredo R, Cardano M, Conti L, Lattante S, Notarangelo A, Sabatelli M, Provenzani A
Generation and characterization of a human iPSC line from an ALS patient carrying the Q66K-MATR3 mutation
Pollini D et al. Generation and characterization of a human iPSC line from an ALS patient carrying the Q66K-MATR3 mutation. . 2018-12-00. Pubmed ID: 30366341; DOI: 10.1016/j.scr.2018.10.011 CIBIOi001-A 2018-12-00 2018-12-00 PubMed: 30366341 DOI: 10.1016/j.scr.2018.10.011Associated cell lines:
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Bluhmki T, Traub S, Schruf E, Garnett J, Gantner F, Bischoff D, Heilker R
Differentiation of hiPS Cells into Definitive Endoderm for High-Throughput Screening
Bluhmki T et al. Differentiation of hiPS Cells into Definitive Endoderm for High-Throughput Screening. . 2019-00-00. Pubmed ID: 31124108; DOI: 10.1007/978-1-4939-9477-9_9 STBCi052-A 2019-00-00 2019-00-00 PubMed: 31124108 DOI: 10.1007/978-1-4939-9477-9_9Associated cell lines:
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Peng GY, Lin Y, Li JJ, Wang Y, Huang HY, Shen ZY
The Application of Induced Pluripotent Stem Cells in Pathogenesis Study and Gene Therapy for Vascular Disorders: Current Progress and Future Challenges
Peng GY et al. The Application of Induced Pluripotent Stem Cells in Pathogenesis Study and Gene Therapy for Vascular Disorders: Current Progress and Future Challenges. . 2019-00-00. Pubmed ID: 31281393; DOI: 10.1155/2019/9613258; PMC: PMC6594248 ISMMSi002-B 2019-00-00 2019-00-00 PubMed: 31281393 DOI: 10.1155/2019/9613258Associated cell lines:
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El-Battrawy I, Müller J, Zhao Z, Cyganek L, Zhong R, Zhang F, Kleinsorge M, Lan H, Li X, Xu Q, Huang M, Liao Z, Moscu-Gregor A, Albers S, Dinkel H, Lang S, Diecke S, Zimmermann WH, Utikal J, Wieland T, Borggrefe M, Zhou X, Akin I
Studying Brugada Syndrome With an SCN1B Variants in Human-Induced Pluripotent Stem Cell-Derived Cardiomyocytes
El-Battrawy I et al. Studying Brugada Syndrome With an SCN1B Variants in Human-Induced Pluripotent Stem Cell-Derived Cardiomyocytes. . 2019-00-00. Pubmed ID: 31737628; DOI: 10.3389/fcell.2019.00261; PMC: PMC6839339 UMGi124-AUMGi128-AUMGi014-B 2019-00-00 2019-00-00 PubMed: 31737628 DOI: 10.3389/fcell.2019.00261 -
Gomez Limia CE, Devalle S, Reis M, Sochacki J, Madeiro da Costa R, D'Andrea M, Padilha T, Zalcberg IR, Solza C, Daumas A, Rehen S, Bonamino MH, Monte-Mór B
Characterization of a human induced Pluripotent Stem (iPS) cell line (INCABRi002-A) derived from a primary myelofibrosis patient harboring the 5-bp insertion in CALR and the p.W146X mutation in TP53
Gomez Limia CE et al. Characterization of a human induced Pluripotent Stem (iPS) cell line (INCABRi002-A) derived from a primary myelofibrosis patient harboring the 5-bp insertion in CALR and the p.W146X mutation in TP53. . 2018-12-00. Pubmed ID: 30343103; DOI: 10.1016/j.scr.2018.09.012 INCABRi002-A 2018-12-00 2018-12-00 PubMed: 30343103 DOI: 10.1016/j.scr.2018.09.012Associated cell lines:
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Hey CAB, Saltõkowa KB, Larsen LJ, Tümer Z, Brøndum-Nielsen K, Grønskov K, Hjortshøj TD, Møller LB
Generation of induced pluripotent stem cells, KCi002-A derived from a patient with Bardet-Biedl syndrome homozygous for the BBS10 variant c.271insT
Hey CAB et al. Generation of induced pluripotent stem cells, KCi002-A derived from a patient with Bardet-Biedl syndrome homozygous for the BBS10 variant c.271insT. . 2018-12-00. Pubmed ID: 30312873; DOI: 10.1016/j.scr.2018.09.013 KCi001-AKCi002-A 2018-12-00 2018-12-00 PubMed: 30312873 DOI: 10.1016/j.scr.2018.09.013 -
Corbett JL, Duncan SA
iPSC-Derived Hepatocytes as a Platform for Disease Modeling and Drug Discovery
Corbett JL et al. iPSC-Derived Hepatocytes as a Platform for Disease Modeling and Drug Discovery. . 2019-00-00. Pubmed ID: 31803747; DOI: 10.3389/fmed.2019.00265; PMC: PMC6873655 TRNDi007-B 2019-00-00 2019-00-00 PubMed: 31803747 DOI: 10.3389/fmed.2019.00265Associated cell lines:
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Hemonnot AL, Hua J, Ulmann L, Hirbec H
Microglia in Alzheimer Disease: Well-Known Targets and New Opportunities
Hemonnot AL et al. Microglia in Alzheimer Disease: Well-Known Targets and New Opportunities. . 2019-00-00. Pubmed ID: 31543810; DOI: 10.3389/fnagi.2019.00233; PMC: PMC6730262 IRMBi001-A 2019-00-00 2019-00-00 PubMed: 31543810 DOI: 10.3389/fnagi.2019.00233Associated cell lines:
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Perriot S, Mathias A, Perriard G, Canales M, Jonkmans N, Merienne N, Meunier C, El Kassar L, Perrier AL, Laplaud DA, Schluep M, Déglon N, Du Pasquier R
Human Induced Pluripotent Stem Cell-Derived Astrocytes Are Differentially Activated by Multiple Sclerosis-Associated Cytokines
Perriot S et al. Human Induced Pluripotent Stem Cell-Derived Astrocytes Are Differentially Activated by Multiple Sclerosis-Associated Cytokines. . 2018-11-13. Pubmed ID: 30409508; DOI: 10.1016/j.stemcr.2018.09.015; PMC: PMC6234919 CHUVi001-ALNISi001-A 2018-11-13 2018-11-13 PubMed: 30409508 DOI: 10.1016/j.stemcr.2018.09.015Associated cell lines:
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Cosentino C, Toivonen S, Diaz Villamil E, Atta M, Ravanat JL, Demine S, Schiavo AA, Pachera N, Deglasse JP, Jonas JC, Balboa D, Otonkoski T, Pearson ER, Marchetti P, Eizirik DL, Cnop M, Igoillo-Esteve M
Pancreatic β-cell tRNA hypomethylation and fragmentation link TRMT10A deficiency with diabetes
Cosentino C et al. Pancreatic β-cell tRNA hypomethylation and fragmentation link TRMT10A deficiency with diabetes. . 2018-11-02. Pubmed ID: 30247717; DOI: 10.1093/nar/gky839; PMC: PMC6212784 ULBi002-AULBi003-A 2018-11-02 2018-11-02 PubMed: 30247717 DOI: 10.1093/nar/gky839 -
Ludwig TE, Kujak A, Rauti A, Andrzejewski S, Langbehn S, Mayfield J, Fuller J, Yashiro Y, Hara Y, Bhattacharyya A
20 Years of Human Pluripotent Stem Cell Research: It All Started with Five Lines
Ludwig TE et al. 20 Years of Human Pluripotent Stem Cell Research: It All Started with Five Lines. . 2018-11-01. Pubmed ID: 30388422; DOI: 10.1016/j.stem.2018.10.009 WAe001-AWAe007-AWAe009-AWAe013-AWAe014-A 2018-11-01 2018-11-01 PubMed: 30388422 DOI: 10.1016/j.stem.2018.10.009 -
Daviaud N, Friedel RH, Zou H
Vascularization and Engraftment of Transplanted Human Cerebral Organoids in Mouse Cortex
Daviaud N et al. Vascularization and Engraftment of Transplanted Human Cerebral Organoids in Mouse Cortex. . 2018-11-00. Pubmed ID: 30460331; DOI: 10.1523/eneuro.0219-18.2018; PMC: PMC6243198 WAe009-A 2018-11-00 2018-11-00 PubMed: 30460331 DOI: 10.1523/eneuro.0219-18.2018Associated cell lines:
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Kutsche LK, Gysi DM, Fallmann J, Lenk K, Petri R, Swiersy A, Klapper SD, Pircs K, Khattak S, Stadler PF, Jakobsson J, Nowick K, Busskamp V
Combined Experimental and System-Level Analyses Reveal the Complex Regulatory Network of miR-124 during Human Neurogenesis
Kutsche LK et al. Combined Experimental and System-Level Analyses Reveal the Complex Regulatory Network of miR-124 during Human Neurogenesis. . 2018-10-24. Pubmed ID: 30292704; DOI: 10.1016/j.cels.2018.08.011; PMC: PMC6205824 CRTDi005-B 2018-10-24 2018-10-24 PubMed: 30292704 DOI: 10.1016/j.cels.2018.08.011Associated cell lines:
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Jones JR, Kong L, Hanna MG 4th, Hoffman B, Krencik R, Bradley R, Hagemann T, Choi J, Doers M, Dubovis M, Sherafat MA, Bhattacharyya A, Kendziorski C, Audhya A, Messing A, Zhang SC
Mutations in GFAP Disrupt the Distribution and Function of Organelles in Human Astrocytes
Jones JR et al. Mutations in GFAP Disrupt the Distribution and Function of Organelles in Human Astrocytes. . 2018-10-23. Pubmed ID: 30355500; DOI: 10.1016/j.celrep.2018.09.083; PMC: PMC6275075 WISCi015-AWISCi015-A-1WISCi016-AWISCi016-A-1 2018-10-23 2018-10-23 PubMed: 30355500 DOI: 10.1016/j.celrep.2018.09.083Associated cell lines:
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Pereira LC, Duarte RB, Maior RS, Barros M
Natural predator and a human stimulus differently affect the behavior, cortisol and cerebral hemisphere activity of marmoset monkeys
Pereira LC et al. Natural predator and a human stimulus differently affect the behavior, cortisol and cerebral hemisphere activity of marmoset monkeys. . 2018-10-15. Pubmed ID: 30063904; DOI: 10.1016/j.physbeh.2018.07.027 ZZUi008-A 2018-10-15 2018-10-15 PubMed: 30063904 DOI: 10.1016/j.physbeh.2018.07.027Associated cell lines:
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Buskin A, Zhu L, Chichagova V, Basu B, Mozaffari-Jovin S, Dolan D, Droop A, Collin J, Bronstein R, Mehrotra S, Farkas M, Hilgen G, White K, Pan KT, Treumann A, Hallam D, Bialas K, Chung G, Mellough C, Ding Y, Krasnogor N, Przyborski S, Zwolinski S, Al-Aama J, Alharthi S, Xu Y, Wheway G, Szymanska K, McKibbin M, Inglehearn CF, Elliott DJ, Lindsay S, Ali RR, Steel DH, Armstrong L, Sernagor E, Urlaub H, Pierce E, Lührmann R, Grellscheid SN, Johnson CA, Lako M
Disrupted alternative splicing for genes implicated in splicing and ciliogenesis causes PRPF31 retinitis pigmentosa
Buskin A et al. Disrupted alternative splicing for genes implicated in splicing and ciliogenesis causes PRPF31 retinitis pigmentosa. . 2018-10-12. Pubmed ID: 30315276; DOI: 10.1038/s41467-018-06448-y; PMC: PMC6185938 UNEWi001-AUNEWi004-AUNEWi005-A 2018-10-12 2018-10-12 PubMed: 30315276 DOI: 10.1038/s41467-018-06448-yAssociated cell lines:
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Harmuth T, Prell-Schicker C, Weber JJ, Gellerich F, Funke C, Drießen S, Magg JCD, Krebiehl G, Wolburg H, Hayer SN, Hauser S, Krüger R, Schöls L, Riess O, Hübener-Schmid J.
Mitochondrial Morphology, Function and Homeostasis Are Impaired by Expression of an N-terminal Calpain Cleavage Fragment of Ataxin-3.
Harmuth T et al. Mitochondrial Morphology, Function and Homeostasis Are Impaired by Expression of an N-terminal Calpain Cleavage Fragment of Ataxin-3. . 2018-10-10. HIHCNi002-A 2018-10-10 2018-10-10Associated cell lines:
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Volpato V, Smith J, Sandor C, Ried JS, Baud A, Handel A, Newey SE, Wessely F, Attar M, Whiteley E, Chintawar S, Verheyen A, Barta T, Lako M, Armstrong L, Muschet C, Artati A, Cusulin C, Christensen K, Patsch C, Sharma E, Nicod J, Brownjohn P, Stubbs V, Heywood WE, Gissen P, De Filippis R, Janssen K, Reinhardt P, Adamski J, Royaux I, Peeters PJ, Terstappen GC, Graf M, Livesey FJ, Akerman CJ, Mills K, Bowden R, Nicholson G, Webber C, Cader MZ, Lakics V
Reproducibility of Molecular Phenotypes after Long-Term Differentiation to Human iPSC-Derived Neurons: A Multi-Site Omics Study
Volpato V et al. Reproducibility of Molecular Phenotypes after Long-Term Differentiation to Human iPSC-Derived Neurons: A Multi-Site Omics Study. . 2018-10-09. Pubmed ID: 30245212; DOI: 10.1016/j.stemcr.2018.08.013; PMC: PMC6178242 STBCi014-BSTBCi322-AUOXFi012-A 2018-10-09 2018-10-09 PubMed: 30245212 DOI: 10.1016/j.stemcr.2018.08.013Associated cell lines:
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Renzova T, Bohaciakova D, Esner M, Pospisilova V, Barta T, Hampl A, Cajanek L
Inactivation of PLK4-STIL Module Prevents Self-Renewal and Triggers p53-Dependent Differentiation in Human Pluripotent Stem Cells
Renzova T et al. Inactivation of PLK4-STIL Module Prevents Self-Renewal and Triggers p53-Dependent Differentiation in Human Pluripotent Stem Cells. . 2018-10-09. Pubmed ID: 30197118; DOI: 10.1016/j.stemcr.2018.08.008; PMC: PMC6178195 MUNIe005-AMUNIe007-A 2018-10-09 2018-10-09 PubMed: 30197118 DOI: 10.1016/j.stemcr.2018.08.008Associated cell lines:
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Trisno SL, Philo KED, McCracken KW, Catá EM, Ruiz-Torres S, Rankin SA, Han L, Nasr T, Chaturvedi P, Rothenberg ME, Mandegar MA, Wells SI, Zorn AM, Wells JM
Esophageal Organoids from Human Pluripotent Stem Cells Delineate Sox2 Functions during Esophageal Specification
Trisno SL et al. Esophageal Organoids from Human Pluripotent Stem Cells Delineate Sox2 Functions during Esophageal Specification. . 2018-10-04. Pubmed ID: 30244869; DOI: 10.1016/j.stem.2018.08.008; PMC: PMC6225525 CUSTOMi001-A 2018-10-04 2018-10-04 PubMed: 30244869 DOI: 10.1016/j.stem.2018.08.008Associated cell lines:
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Husa AM, Strobl MR, Strajeriu A, Wieser M, Strehl S, Fortschegger K
Generation of CD34 Fluorescent Reporter Human Induced Pluripotent Stem Cells for Monitoring Hematopoietic Differentiation
Husa AM et al. Generation of CD34 Fluorescent Reporter Human Induced Pluripotent Stem Cells for Monitoring Hematopoietic Differentiation. . 2018-10-01. Pubmed ID: 30009677; DOI: 10.1089/scd.2018.0093 TMOi001-ATMOi001-A-1 2018-10-01 2018-10-01 PubMed: 30009677 DOI: 10.1089/scd.2018.0093Associated cell lines:
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Zhu X, Cai A, Meng J, Liu L, Cui S, Qu S, Zhao J, Liu N, Kong X
Generation of ZZUi008-A, a transgene-free, induced pluripotent stem cell line derived from chorionic villi cells of a fetus with Duchenne muscular dystrophy
Zhu X et al. Generation of ZZUi008-A, a transgene-free, induced pluripotent stem cell line derived from chorionic villi cells of a fetus with Duchenne muscular dystrophy. . 2018-10-00. Pubmed ID: 30172907; DOI: 10.1016/j.scr.2018.07.017 ZZUi008-A 2018-10-00 2018-10-00 PubMed: 30172907 DOI: 10.1016/j.scr.2018.07.017Associated cell lines:
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Turco EM, Vinci E, Altieri F, Ferrari D, Torres B, Goldoni M, Lamorte G, Tata AM, Mazzoccoli G, Postorivo D, Della Monica M, Bernardini L, Vescovi AL, Rosati J
Copy number variations in healthy subjects. Case study: iPSC line CSSi005-A (3544) production from an individual with variation in 15q13.3 chromosome duplicating gene CHRNA7
Turco EM et al. Copy number variations in healthy subjects. Case study: iPSC line CSSi005-A (3544) production from an individual with variation in 15q13.3 chromosome duplicating gene CHRNA7. . 2018-10-00. Pubmed ID: 30218896; DOI: 10.1016/j.scr.2018.09.002 CSSi005-A 2018-10-00 2018-10-00 PubMed: 30218896 DOI: 10.1016/j.scr.2018.09.002Associated cell lines:
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Gaspari E, Franke A, Robles-Diaz D, Zweigerdt R, Roeder I, Zerjatke T, Kempf H
Paracrine mechanisms in early differentiation of human pluripotent stem cells: Insights from a mathematical model
Gaspari E et al. Paracrine mechanisms in early differentiation of human pluripotent stem cells: Insights from a mathematical model. . 2018-10-00. Pubmed ID: 30145492; DOI: 10.1016/j.scr.2018.07.025 ESIBIe003-A 2018-10-00 2018-10-00 PubMed: 30145492 DOI: 10.1016/j.scr.2018.07.025Associated cell lines:
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Palladino VS, Subrata NOC, Geburtig-Chiocchetti A, McNeill R, Hoffmann P, Reif A, Kittel-Schneider S
Generation of human induced pluripotent stem cell lines (hiPSC) from one bipolar disorder patient carrier of a DGKH risk haplotype and one non-risk-variant-carrier bipolar disorder patient
Palladino VS et al. Generation of human induced pluripotent stem cell lines (hiPSC) from one bipolar disorder patient carrier of a DGKH risk haplotype and one non-risk-variant-carrier bipolar disorder patient. . 2018-10-00. Pubmed ID: 30266033; DOI: 10.1016/j.scr.2018.09.008 KGUi001-AKGUi002-A 2018-10-00 2018-10-00 PubMed: 30266033 DOI: 10.1016/j.scr.2018.09.008 -
Ermon B, Volpato CB, Cattelan G, Silipigni R, Di Segni M, Cantaloni C, Casella M, Pramstaller PP, Pompilio G, Sommariva E, Meraviglia V, Rossini A
Derivation of human induced pluripotent stem cell line EURACi004-A from skin fibroblasts of a patient with Arrhythmogenic Cardiomyopathy carrying the heterozygous PKP2 mutation c.2569_3018del50
Ermon B et al. Derivation of human induced pluripotent stem cell line EURACi004-A from skin fibroblasts of a patient with Arrhythmogenic Cardiomyopathy carrying the heterozygous PKP2 mutation c.2569_3018del50. . 2018-10-00. Pubmed ID: 30219716; DOI: 10.1016/j.scr.2018.09.003; PMC: PMC6189521 EURACi004-AINEUi002-A-1 2018-10-00 2018-10-00 PubMed: 30219716 DOI: 10.1016/j.scr.2018.09.003Associated cell lines:
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Wang Y, Kang C, Yu H, Fen J, Ma X, Lei Y, Zhao J
Establishment of TUSMi004-A, an induced pluripotent stem cell (iPSC) line from a 32-year old Chinese Han patient with Obsessive-Compulsive Disorder (OCD)
Wang Y et al. Establishment of TUSMi004-A, an induced pluripotent stem cell (iPSC) line from a 32-year old Chinese Han patient with Obsessive-Compulsive Disorder (OCD). . 2018-10-00. Pubmed ID: 30223146; DOI: 10.1016/j.scr.2018.08.020 TUSMi004-A 2018-10-00 2018-10-00 PubMed: 30223146 DOI: 10.1016/j.scr.2018.08.020Associated cell lines:
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Vallejo S, Fleischer A, Martín JM, Sánchez A, Palomino E, Bachiller D
Generation of two induced pluripotent stem cells lines from Mucopolysaccharydosis IIIA patient: IMEDEAi004-A and IMEDEAi004-B
Vallejo S et al. Generation of two induced pluripotent stem cells lines from Mucopolysaccharydosis IIIA patient: IMEDEAi004-A and IMEDEAi004-B. . 2018-10-00. Pubmed ID: 30269021; DOI: 10.1016/j.scr.2018.09.009 IMEDEAi004-AIMEDEAi004-B 2018-10-00 2018-10-00 PubMed: 30269021 DOI: 10.1016/j.scr.2018.09.009Associated cell lines:
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Wang Y, Wang Z, Sun H, Shi C, Yang J, Liu Y, Liu H, Zhang S, Zhang L, Xu Y, Zhang J
Generation of induced pluripotent stem cell line(ZZUi006-A)from a patient with myotonic dystrophy type 1
Wang Y et al. Generation of induced pluripotent stem cell line(ZZUi006-A)from a patient with myotonic dystrophy type 1. . 2018-10-00. Pubmed ID: 30216892; DOI: 10.1016/j.scr.2018.08.013 CHUQi001-AZZUi006-A 2018-10-00 2018-10-00 PubMed: 30216892 DOI: 10.1016/j.scr.2018.08.013Associated cell lines:
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Fujimori K, Ishikawa M, Otomo A, Atsuta N, Nakamura R, Akiyama T, Hadano S, Aoki M, Saya H, Sobue G, Okano H
Modeling sporadic ALS in iPSC-derived motor neurons identifies a potential therapeutic agent
Fujimori K et al. Modeling sporadic ALS in iPSC-derived motor neurons identifies a potential therapeutic agent. . 2018-10-00. Pubmed ID: 30127392; DOI: 10.1038/s41591-018-0140-5 KUIFMSi004-CCIRAi007-A 2018-10-00 2018-10-00 PubMed: 30127392 DOI: 10.1038/s41591-018-0140-5Associated cell lines:
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Fischer B, Meier A, Dehne A, Salhotra A, Tran TA, Neumann S, Schmidt K, Meiser I, Neubauer JC, Zimmermann H, Gentile L
A complete workflow for the differentiation and the dissociation of hiPSC-derived cardiospheres
Fischer B et al. A complete workflow for the differentiation and the dissociation of hiPSC-derived cardiospheres. . 2018-10-00. Pubmed ID: 30218895; DOI: 10.1016/j.scr.2018.08.015 UKBi005-A 2018-10-00 2018-10-00 PubMed: 30218895 DOI: 10.1016/j.scr.2018.08.015Associated cell lines:
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Engel M, Balez R, Muñoz SS, Cabral-da-Silva MC, Stevens CH, Bax M, Do-Ha D, Sidhu K, Sachdev P, Ooi L
Viral-free generation and characterization of a human induced pluripotent stem cell line from dermal fibroblasts
Engel M et al. Viral-free generation and characterization of a human induced pluripotent stem cell line from dermal fibroblasts. . 2018-10-00. Pubmed ID: 30278375; DOI: 10.1016/j.scr.2018.09.014 UOWi001-A 2018-10-00 2018-10-00 PubMed: 30278375 DOI: 10.1016/j.scr.2018.09.014Associated cell lines:
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Wang Y, Wang Z, Sun H, Mao C, Yang J, Liu Y, Liu H, Zhang S, Zhang J, Xu Y, Shi C
Generation of induced pluripotent stem cell line (ZZUi007-A) from a 52-year-old patient with a novel CHCHD2 gene mutation in Parkinson's disease
Wang Y et al. Generation of induced pluripotent stem cell line (ZZUi007-A) from a 52-year-old patient with a novel CHCHD2 gene mutation in Parkinson's disease. . 2018-10-00. Pubmed ID: 30237140; DOI: 10.1016/j.scr.2018.08.011 ZZUi007-A 2018-10-00 2018-10-00 PubMed: 30237140 DOI: 10.1016/j.scr.2018.08.011Associated cell lines:
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Brookhouser N, Zhang P, Caselli R, Kim JJ, Brafman DA
Generation and characterization of two human induced pluripotent stem cell (hiPSC) lines homozygous for the Apolipoprotein e4 (APOE4) risk variant-Alzheimer's disease (ASUi005-A) and healthy non-demented control (ASUi006-A)
Brookhouser N et al. Generation and characterization of two human induced pluripotent stem cell (hiPSC) lines homozygous for the Apolipoprotein e4 (APOE4) risk variant-Alzheimer's disease (ASUi005-A) and healthy non-demented control (ASUi006-A). . 2018-10-00. Pubmed ID: 30296667; DOI: 10.1016/j.scr.2018.09.007; PMC: PMC6217860 ASUi005-AASUi006-A 2018-10-00 2018-10-00 PubMed: 30296667 DOI: 10.1016/j.scr.2018.09.007 -
Osaki T, Uzel SGM, Kamm RD
Microphysiological 3D model of amyotrophic lateral sclerosis (ALS) from human iPS-derived muscle cells and optogenetic motor neurons
Osaki T et al. Microphysiological 3D model of amyotrophic lateral sclerosis (ALS) from human iPS-derived muscle cells and optogenetic motor neurons. . 2018-10-00. Pubmed ID: 30324134; DOI: 10.1126/sciadv.aat5847; PMC: PMC6179377 WAe009-ACDIi001-A 2018-10-00 2018-10-00 PubMed: 30324134 DOI: 10.1126/sciadv.aat5847 -
Wei R, Yuan F, Wu Y, Liu Y, You K, Yang Z, Chen Y, Getachew A, Wang N, Xu Y, Zhuang Y, Yang F, Li YX
Construction of a GLI3 compound heterozygous knockout human embryonic stem cell line WAe001-A-20 by CRISPR/Cas9 editing
Wei R et al. Construction of a GLI3 compound heterozygous knockout human embryonic stem cell line WAe001-A-20 by CRISPR/Cas9 editing. . 2018-10-00. Pubmed ID: 30278376; DOI: 10.1016/j.scr.2018.09.010 WAe001-AWAe001-A-20 2018-10-00 2018-10-00 PubMed: 30278376 DOI: 10.1016/j.scr.2018.09.010Associated cell lines:
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Potirat P, Wattanapanitch M, Kheolamai P, Issaragrisil S
Establishment of a human iPSC line (MUSIi007-A) from peripheral blood of normal individual using Sendai viral vectors
Potirat P et al. Establishment of a human iPSC line (MUSIi007-A) from peripheral blood of normal individual using Sendai viral vectors. . 2018-10-00. Pubmed ID: 30172906; DOI: 10.1016/j.scr.2018.08.014 MUSIi007-A 2018-10-00 2018-10-00 PubMed: 30172906 DOI: 10.1016/j.scr.2018.08.014Associated cell lines:
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Lee S, Huh JY, Turner DM, Lee S, Robinson J, Stein JE, Shim SH, Hong CP, Kang MS, Nakagawa M, Kaneko S, Nakanishi M, Rao MS, Kurtz A, Stacey GN, Marsh SGE, Turner ML, Song J
Repurposing the Cord Blood Bank for Haplobanking of HLA-Homozygous iPSCs and Their Usefulness to Multiple Populations
Lee S et al. Repurposing the Cord Blood Bank for Haplobanking of HLA-Homozygous iPSCs and Their Usefulness to Multiple Populations. . 2018-10-00. Pubmed ID: 30004605; DOI: 10.1002/stem.2865 CHAi001-ACHAi002-ACHAi003-ACHAi004-ACHAi005-ACHAi006-ACHAi007-ACHAi008-ACHAi009-ACHAi010-A 2018-10-00 2018-10-00 PubMed: 30004605 DOI: 10.1002/stem.2865 -
Re S, Dogan AA, Ben-Shachar D, Berger G, Werling AM, Walitza S, Grünblatt E.
Improved Generation of Induced Pluripotent Stem Cells From Hair Derived Keratinocytes – A Tool to Study Neurodevelopmental Disorders as ADHD.
Re S et al. Improved Generation of Induced Pluripotent Stem Cells From Hair Derived Keratinocytes – A Tool to Study Neurodevelopmental Disorders as ADHD. . 2018-09-25. MUSIi006-A 2018-09-25 2018-09-25Associated cell lines:
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Buchrieser J, Oliva-Martin MJ, Moore MD, Long JCD, Cowley SA, Perez-Simón JA, James W, Venero JL
RIPK1 is a critical modulator of both tonic and TLR-responsive inflammatory and cell death pathways in human macrophage differentiation
Buchrieser J et al. RIPK1 is a critical modulator of both tonic and TLR-responsive inflammatory and cell death pathways in human macrophage differentiation. . 2018-09-24. Pubmed ID: 30250197; DOI: 10.1038/s41419-018-1053-4; PMC: PMC6155173 STBCi044-A 2018-09-24 2018-09-24 PubMed: 30250197 DOI: 10.1038/s41419-018-1053-4Associated cell lines:
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Chan CKF, Gulati GS, Sinha R, Tompkins JV, Lopez M, Carter AC, Ransom RC, Reinisch A, Wearda T, Murphy M, Brewer RE, Koepke LS, Marecic O, Manjunath A, Seo EY, Leavitt T, Lu WJ, Nguyen A, Conley SD, Salhotra A, Ambrosi TH, Borrelli MR, Siebel T, Chan K, Schallmoser K, Seita J, Sahoo D, Goodnough H, Bishop J, Gardner M, Majeti R, Wan DC, Goodman S, Weissman IL, Chang HY, Longaker MT
Identification of the Human Skeletal Stem Cell
Chan CKF et al. Identification of the Human Skeletal Stem Cell. . 2018-09-20. Pubmed ID: 30241615; DOI: 10.1016/j.cell.2018.07.029; PMC: PMC6400492 BIHi050-A 2018-09-20 2018-09-20 PubMed: 30241615 DOI: 10.1016/j.cell.2018.07.029Associated cell lines:
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Meyer K, Kirchner M, Uyar B, Cheng JY, Russo G, Hernandez-Miranda LR, Szymborska A, Zauber H, Rudolph IM, Willnow TE, Akalin A, Haucke V, Gerhardt H, Birchmeier C, Kühn R, Krauss M, Diecke S, Pascual JM, Selbach M
Mutations in Disordered Regions Can Cause Disease by Creating Dileucine Motifs
Meyer K et al. Mutations in Disordered Regions Can Cause Disease by Creating Dileucine Motifs. . 2018-09-20. Pubmed ID: 30197081; DOI: 10.1016/j.cell.2018.08.019 BIHi037-ABIHi037-BBIHi037-CBIHi037-DBIHi037-E 2018-09-20 2018-09-20 PubMed: 30197081 DOI: 10.1016/j.cell.2018.08.019 -
D'Amario D, Gowran A, Canonico F, Castiglioni E, Rovina D, Santoro R, Spinelli P, Adorisio R, Amodeo A, Perrucci GL, Borovac JA, Pompilio G, Crea F
Dystrophin Cardiomyopathies: Clinical Management, Molecular Pathogenesis and Evolution towards Precision Medicine
D'Amario D et al. Dystrophin Cardiomyopathies: Clinical Management, Molecular Pathogenesis and Evolution towards Precision Medicine. . 2018-09-19. Pubmed ID: 30235804; DOI: 10.3390/jcm7090291; PMC: PMC6162458 IITi001-A 2018-09-19 2018-09-19 PubMed: 30235804 DOI: 10.3390/jcm7090291Associated cell lines:
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Vu M, Li R, Baskfield A, Lu B, Farkhondeh A, Gorshkov K, Motabar O, Beers J, Chen G, Zou J, Espejo-Mojica AJ, Rodríguez-López A, Alméciga-Díaz CJ, Barrera LA, Jiang X, Ory DS, Marugan JJ, Zheng W
Neural stem cells for disease modeling and evaluation of therapeutics for Tay-Sachs disease
Vu M et al. Neural stem cells for disease modeling and evaluation of therapeutics for Tay-Sachs disease. . 2018-09-17. Pubmed ID: 30220252; DOI: 10.1186/s13023-018-0886-3; PMC: PMC6139903 TRNDi028-A 2018-09-17 2018-09-17 PubMed: 30220252 DOI: 10.1186/s13023-018-0886-3Associated cell lines:
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Rosati J, Ferrari D, Altieri F, Tardivo S, Ricciolini C, Fusilli C, Zalfa C, Profico DC, Pinos F, Bernardini L, Torres B, Manni I, Piaggio G, Binda E, Copetti M, Lamorte G, Mazza T, Carella M, Gelati M, Valente EM, Simeone A, Vescovi AL
Establishment of stable iPS-derived human neural stem cell lines suitable for cell therapies
Rosati J et al. Establishment of stable iPS-derived human neural stem cell lines suitable for cell therapies. . 2018-09-17. Pubmed ID: 30224709; DOI: 10.1038/s41419-018-0990-2; PMC: PMC6141489 CSSi001-ACSSi002-A 2018-09-17 2018-09-17 PubMed: 30224709 DOI: 10.1038/s41419-018-0990-2 -
Golas MM
Human cellular models of medium spiny neuron development and Huntington disease
Golas MM. Human cellular models of medium spiny neuron development and Huntington disease. . 2018-09-15. Pubmed ID: 30031060; DOI: 10.1016/j.lfs.2018.07.030 CSSi002-A 2018-09-15 2018-09-15 PubMed: 30031060 DOI: 10.1016/j.lfs.2018.07.030Associated cell lines:
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Gyllborg D, Ahmed M, Toledo EM, Theofilopoulos S, Yang S, Ffrench-Constant C, Arenas E
The Matricellular Protein R-Spondin 2 Promotes Midbrain Dopaminergic Neurogenesis and Differentiation
Gyllborg D et al. The Matricellular Protein R-Spondin 2 Promotes Midbrain Dopaminergic Neurogenesis and Differentiation. . 2018-09-11. Pubmed ID: 30146491; DOI: 10.1016/j.stemcr.2018.07.014; PMC: PMC6135723 RCe021-A 2018-09-11 2018-09-11 PubMed: 30146491 DOI: 10.1016/j.stemcr.2018.07.014Associated cell lines:
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Xiang X, Piers TM, Wefers B, Zhu K, Mallach A, Brunner B, Kleinberger G, Song W, Colonna M, Herms J, Wurst W, Pocock JM, Haass C
The Trem2 R47H Alzheimer's risk variant impairs splicing and reduces Trem2 mRNA and protein in mice but not in humans
Xiang X et al. The Trem2 R47H Alzheimer's risk variant impairs splicing and reduces Trem2 mRNA and protein in mice but not in humans. . 2018-09-06. Pubmed ID: 30185230; DOI: 10.1186/s13024-018-0280-6; PMC: PMC6126019 BIONi010-CSTBCi322-A 2018-09-06 2018-09-06 PubMed: 30185230 DOI: 10.1186/s13024-018-0280-6Associated cell lines:
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Froese N, Wang H, Zwadlo C, Wang Y, Grund A, Gigina A, Hofmann M, Kilian K, Scharf G, Korf-Klingebiel M, Melchert A, Signorini MER, Halloin C, Zweigerdt R, Martin U, Gruh I, Wollert KC, Geffers R, Bauersachs J, Heineke J
Anti-androgenic therapy with finasteride improves cardiac function, attenuates remodeling and reverts pathologic gene-expression after myocardial infarction in mice
Froese N et al. Anti-androgenic therapy with finasteride improves cardiac function, attenuates remodeling and reverts pathologic gene-expression after myocardial infarction in mice. . 2018-09-00. Pubmed ID: 30118791; DOI: 10.1016/j.yjmcc.2018.08.011 MHHi001-A 2018-09-00 2018-09-00 PubMed: 30118791 DOI: 10.1016/j.yjmcc.2018.08.011Associated cell lines:
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Garcia-Reitboeck P, Phillips A, Piers TM, Villegas-Llerena C, Butler M, Mallach A, Rodrigues C, Arber CE, Heslegrave A, Zetterberg H, Neumann H, Neame S, Houlden H, Hardy J, Pocock JM
Human Induced Pluripotent Stem Cell-Derived Microglia-Like Cells Harboring TREM2 Missense Mutations Show Specific Deficits in Phagocytosis
Garcia-Reitboeck P et al. Human Induced Pluripotent Stem Cell-Derived Microglia-Like Cells Harboring TREM2 Missense Mutations Show Specific Deficits in Phagocytosis. . 2018-08-28. Pubmed ID: 30157425; DOI: 10.1016/j.celrep.2018.07.094; PMC: PMC6130048 STBCi026-BSTBCi322-A 2018-08-28 2018-08-28 PubMed: 30157425 DOI: 10.1016/j.celrep.2018.07.094Associated cell lines:
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Haupt A, Grancharova T, Arakaki J, Fuqua MA, Roberts B, Gunawardane RN
Endogenous Protein Tagging in Human Induced Pluripotent Stem Cells Using CRISPR/Cas9
Haupt A et al. Endogenous Protein Tagging in Human Induced Pluripotent Stem Cells Using CRISPR/Cas9. . 2018-08-25. Pubmed ID: 30199041; DOI: 10.3791/58130; PMC: PMC6231893 UCSFi001-AUCSFi001-A-6 2018-08-25 2018-08-25 PubMed: 30199041 DOI: 10.3791/58130Associated cell lines:
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Simão D, Silva MM, Terrasso AP, Arez F, Sousa MFQ, Mehrjardi NZ, Šarić T, Gomes-Alves P, Raimundo N, Alves PM, Brito C
Recapitulation of Human Neural Microenvironment Signatures in iPSC-Derived NPC 3D Differentiation
Simão D et al. Recapitulation of Human Neural Microenvironment Signatures in iPSC-Derived NPC 3D Differentiation. . 2018-08-14. Pubmed ID: 30057262; DOI: 10.1016/j.stemcr.2018.06.020; PMC: PMC6094163 RIi001-ARIi007-A 2018-08-14 2018-08-14 PubMed: 30057262 DOI: 10.1016/j.stemcr.2018.06.020 -
Guhr A, Kobold S, Seltmann S, Seiler Wulczyn AEM, Kurtz A, Löser P
Recent Trends in Research with Human Pluripotent Stem Cells: Impact of Research and Use of Cell Lines in Experimental Research and Clinical Trials
Guhr A et al. Recent Trends in Research with Human Pluripotent Stem Cells: Impact of Research and Use of Cell Lines in Experimental Research and Clinical Trials. . 2018-08-14. Pubmed ID: 30033087; DOI: 10.1016/j.stemcr.2018.06.012; PMC: PMC6092712 KIe001-AHVRDe001-AHVRDe003-AHVRDe006-AHVRDe007-AHVRDe008-AHVRDe009-ASCSe001-AWAe001-AWAe007-AWAe009-AWAe013-AWAe014-AVIACe001-AESIBIe002-AESIBIe003-AUCSFe002-AKUIMSe001-AKUIMSe003-AMSHRIe001-A 2018-08-14 2018-08-14 PubMed: 30033087 DOI: 10.1016/j.stemcr.2018.06.012 -
Verheyen A, Diels A, Reumers J, Van Hoorde K, Van den Wyngaert I, van Outryve d'Ydewalle C, De Bondt A, Kuijlaars J, De Muynck L, De Hoogt R, Bretteville A, Jaensch S, Buist A, Cabrera-Socorro A, Wray S, Ebneth A, Roevens P, Royaux I, Peeters PJ
Genetically Engineered iPSC-Derived FTDP-17 MAPT Neurons Display Mutation-Specific Neurodegenerative and Neurodevelopmental Phenotypes
Verheyen A et al. Genetically Engineered iPSC-Derived FTDP-17 MAPT Neurons Display Mutation-Specific Neurodegenerative and Neurodevelopmental Phenotypes. . 2018-08-14. Pubmed ID: 30057263; DOI: 10.1016/j.stemcr.2018.06.022; PMC: PMC6093179 SIGi001-ASIGi001-A-9SIGi001-A-12SIGi001-A-13 2018-08-14 2018-08-14 PubMed: 30057263 DOI: 10.1016/j.stemcr.2018.06.022Associated cell lines:
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Kho J, Tian X, Wong WT, Bertin T, Jiang MM, Chen S, Jin Z, Shchelochkov OA, Burrage LC, Reddy AK, Jiang H, Abo-Zahrah R, Ma S, Zhang P, Bissig KD, Kim JJ, Devaraj S, Rodney GG, Erez A, Bryan NS, Nagamani SCS, Lee BH
Argininosuccinate Lyase Deficiency Causes an Endothelial-Dependent Form of Hypertension
Kho J et al. Argininosuccinate Lyase Deficiency Causes an Endothelial-Dependent Form of Hypertension. . 2018-08-02. Pubmed ID: 30075114; DOI: 10.1016/j.ajhg.2018.07.008; PMC: PMC6080833 BCMi001-ABCMi001-B 2018-08-02 2018-08-02 PubMed: 30075114 DOI: 10.1016/j.ajhg.2018.07.008 -
Happle C, Lachmann N, Ackermann M, Mirenska A, Göhring G, Thomay K, Mucci A, Hetzel M, Glomb T, Suzuki T, Chalk C, Glage S, Dittrich-Breiholz O, Trapnell B, Moritz T, Hansen G
Pulmonary Transplantation of Human Induced Pluripotent Stem Cell-derived Macrophages Ameliorates Pulmonary Alveolar Proteinosis
Happle C et al. Pulmonary Transplantation of Human Induced Pluripotent Stem Cell-derived Macrophages Ameliorates Pulmonary Alveolar Proteinosis. . 2018-08-01. Pubmed ID: 29652170; DOI: 10.1164/rccm.201708-1562oc; PMC: PMC6835058 MHHi015-A 2018-08-01 2018-08-01 PubMed: 29652170 DOI: 10.1164/rccm.201708-1562ocAssociated cell lines:
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Zurita-Díaz F, Ortuño-Costela MDC, Moreno-Izquierdo A, Galbis L, Millán JM, Ayuso C, Garesse R, Gallardo ME
Establishment of a human iPSC line, IISHDOi004-A, from a patient with Usher syndrome associated with the mutation c.2276G>T; p.Cys759Phe in the USH2A gene
Zurita-Díaz F et al. Establishment of a human iPSC line, IISHDOi004-A, from a patient with Usher syndrome associated with the mutation c.2276G>T; p.Cys759Phe in the USH2A gene. . 2018-08-00. Pubmed ID: 30096711; DOI: 10.1016/j.scr.2018.08.002 IISHDOi004-A 2018-08-00 2018-08-00 PubMed: 30096711 DOI: 10.1016/j.scr.2018.08.002Associated cell lines:
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Wang Y, Yu H, Chen Y, Li G, Lei Y, Zhao J
Derivation of induced pluripotent stem cells TUSMi006 from an 87-year old Chinese Han Alzheimer's disease patient carrying GRINB and SORL1 mutations
Wang Y et al. Derivation of induced pluripotent stem cells TUSMi006 from an 87-year old Chinese Han Alzheimer's disease patient carrying GRINB and SORL1 mutations. . 2018-08-00. Pubmed ID: 30077089; DOI: 10.1016/j.scr.2018.07.018 TUSMi006-A 2018-08-00 2018-08-00 PubMed: 30077089 DOI: 10.1016/j.scr.2018.07.018Associated cell lines:
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Gao X, Yourick JJ, Sprando RL
Generation of nine induced pluripotent stem cell lines as an ethnic diversity panel
Gao X et al. Generation of nine induced pluripotent stem cell lines as an ethnic diversity panel. . 2018-08-00. Pubmed ID: 30099336; DOI: 10.1016/j.scr.2018.07.013 OARSAi001-AOARSAi002-AOARSAi003-AOARSAi004-AOARSAi005-AOARSAi006-AOARSAi007-AOARSAi008-AOARSAi009-A 2018-08-00 2018-08-00 PubMed: 30099336 DOI: 10.1016/j.scr.2018.07.013Associated cell lines:
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Ntai A, La Spada A, De Blasio P, Biunno I
Trehalose to cryopreserve human pluripotent stem cells
Ntai A et al. Trehalose to cryopreserve human pluripotent stem cells. . 2018-08-00. Pubmed ID: 30071393; DOI: 10.1016/j.scr.2018.07.021 RCe021-A 2018-08-00 2018-08-00 PubMed: 30071393 DOI: 10.1016/j.scr.2018.07.021Associated cell lines:
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Li H, Pei H, Nie J, Qu M, Fan Z, Jia Y, He L, Nan X, Yue W, Pei X
Integration-free reprogramming of human umbilical arterial endothelial cells into induced pluripotent stem cells IHSTMi001-A
Li H et al. Integration-free reprogramming of human umbilical arterial endothelial cells into induced pluripotent stem cells IHSTMi001-A. . 2018-08-00. Pubmed ID: 30138849; DOI: 10.1016/j.scr.2018.08.007 IHSTMi001-A 2018-08-00 2018-08-00 PubMed: 30138849 DOI: 10.1016/j.scr.2018.08.007Associated cell lines:
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Tanaka Y, Higurashi N, Shirasu N, Yasunaga S, Moreira KM, Okano H, Hirose S
Establishment of a human induced stem cell line (FUi002-A) from Dravet syndrome patient carrying heterozygous R1525X mutation in SCN1A gene
Tanaka Y et al. Establishment of a human induced stem cell line (FUi002-A) from Dravet syndrome patient carrying heterozygous R1525X mutation in SCN1A gene. . 2018-08-00. Pubmed ID: 29981888; DOI: 10.1016/j.scr.2018.06.008 FUi002-A 2018-08-00 2018-08-00 PubMed: 29981888 DOI: 10.1016/j.scr.2018.06.008Associated cell lines:
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Wang H, Zhao S, Finnell RH, George T, Cooney AJ
Generation of integration-free induced pluripotent stem cells from a patient with spina bifida
Wang H et al. Generation of integration-free induced pluripotent stem cells from a patient with spina bifida. . 2018-08-00. Pubmed ID: 30007220; DOI: 10.1016/j.scr.2018.05.007 DUTi001-A 2018-08-00 2018-08-00 PubMed: 30007220 DOI: 10.1016/j.scr.2018.05.007Associated cell lines:
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Oksanen M, Hyötyläinen I, Voutilainen J, Puttonen KA, Hämäläinen RH, Graff C, Lehtonen Š, Koistinaho J
Generation of a human induced pluripotent stem cell line (LL008 1.4) from a familial Alzheimer's disease patient carrying a double KM670/671NL (Swedish) mutation in APP gene
Oksanen M et al. Generation of a human induced pluripotent stem cell line (LL008 1.4) from a familial Alzheimer's disease patient carrying a double KM670/671NL (Swedish) mutation in APP gene. . 2018-08-00. Pubmed ID: 30099334; DOI: 10.1016/j.scr.2018.07.024 UEFi002-A 2018-08-00 2018-08-00 PubMed: 30099334 DOI: 10.1016/j.scr.2018.07.024Associated cell lines:
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Kasai-Brunswick TH, Silva Dos Santos D, Ferreira RP, Araujo DS, Dias GM, Coutinho JLA, Cruz FESF, Sternick EB, Gubert F, Oliveira JCG, Vaz IM, Borgonovo T, Brofman PRS, Moura-Neto RS, Silva R, Campos-de-Carvalho AC, Carvalho AB
Generation of patient-specific induced pluripotent stem cell lines from one patient with Jervell and Lange-Nielsen syndrome, one with type 1 long QT syndrome and two healthy relatives
Kasai-Brunswick TH et al. Generation of patient-specific induced pluripotent stem cell lines from one patient with Jervell and Lange-Nielsen syndrome, one with type 1 long QT syndrome and two healthy relatives. . 2018-08-00. Pubmed ID: 30099333; DOI: 10.1016/j.scr.2018.07.016 UFRJi001-AUFRJi002-AUFRJi003-AUFRJi004-A 2018-08-00 2018-08-00 PubMed: 30099333 DOI: 10.1016/j.scr.2018.07.016Associated cell lines:
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Klein T, Günther K, Kwok CK, Edenhofer F, Üçeyler N
Generation of the human induced pluripotent stem cell line (UKWNLi001-A) from skin fibroblasts of a woman with Fabry disease carrying the X-chromosomal heterozygous c.708 G > C (W236C) missense mutation in exon 5 of the alpha-galactosidase-A gene
Klein T et al. Generation of the human induced pluripotent stem cell line (UKWNLi001-A) from skin fibroblasts of a woman with Fabry disease carrying the X-chromosomal heterozygous c.708 G > C (W236C) missense mutation in exon 5 of the alpha-galactosidase-A gene. . 2018-08-00. Pubmed ID: 30130681; DOI: 10.1016/j.scr.2018.08.009 UKWNLi001-A 2018-08-00 2018-08-00 PubMed: 30130681 DOI: 10.1016/j.scr.2018.08.009Associated cell lines:
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Hey CAB, Saltõkowa KB, Larsen LJ, Tümer Z, Brøndum-Nielsen K, Grønskov K, Hjortshøj TD, Møller LB
Generation of induced pluripotent stem cells, KCi001-A derived from a Bardet-Biedl syndrome patient compound heterozygous for the BBS1 variants c.1169T>G/c.1135G>C
Hey CAB et al. Generation of induced pluripotent stem cells, KCi001-A derived from a Bardet-Biedl syndrome patient compound heterozygous for the BBS1 variants c.1169T>G/c.1135G>C. . 2018-08-00. Pubmed ID: 30142598; DOI: 10.1016/j.scr.2018.08.005 KCi001-A 2018-08-00 2018-08-00 PubMed: 30142598 DOI: 10.1016/j.scr.2018.08.005Associated cell lines:
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Arellano CM, Vilches A, Clemente E, Pascual-Pascual SI, Bolinches-Amorós A, Castro AA, Espinos C, Rodriguez ML, Jendelova P, Erceg S
Generation of a human iPSC line from a patient with autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) caused by mutation in SACSIN gene
Arellano CM et al. Generation of a human iPSC line from a patient with autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) caused by mutation in SACSIN gene. . 2018-08-00. Pubmed ID: 30144656; DOI: 10.1016/j.scr.2018.07.012 ESi043-AESi063-A 2018-08-00 2018-08-00 PubMed: 30144656 DOI: 10.1016/j.scr.2018.07.012 -
Muñoz SS, Balez R, Castro Cabral-da-Silva ME, Berg T, Engel M, Bax M, Do-Ha D, Stevens CH, Greenough M, Bush A, Ooi L
Generation and characterization of human induced pluripotent stem cell lines from a familial Alzheimer's disease PSEN1 A246E patient and a non-demented family member bearing wild-type PSEN1
Muñoz SS et al. Generation and characterization of human induced pluripotent stem cell lines from a familial Alzheimer's disease PSEN1 A246E patient and a non-demented family member bearing wild-type PSEN1. . 2018-08-00. Pubmed ID: 30138848; DOI: 10.1016/j.scr.2018.08.006 UOWi002-AUOWi003-A 2018-08-00 2018-08-00 PubMed: 30138848 DOI: 10.1016/j.scr.2018.08.006 -
Graffmann N, Bohndorf M, Ncube A, Kawala MA, Wruck W, Kashofer K, Zatloukal K, Adjaye J
Establishment and characterization of an iPSC line from a 35 years old high grade patient with nonalcoholic fatty liver disease (30-40% steatosis) with homozygous wildtype PNPLA3 genotype
Graffmann N et al. Establishment and characterization of an iPSC line from a 35 years old high grade patient with nonalcoholic fatty liver disease (30-40% steatosis) with homozygous wildtype PNPLA3 genotype. . 2018-08-00. Pubmed ID: 30071394; DOI: 10.1016/j.scr.2018.07.015 HHUUKDi008-A 2018-08-00 2018-08-00 PubMed: 30071394 DOI: 10.1016/j.scr.2018.07.015Associated cell lines:
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Kumar D, Hussain A, Srivastava AK, Mukerji M, Mukherjee O, Faruq M
Generation of three spinocerebellar ataxia type-12 patients derived induced pluripotent stem cell lines (IGIBi002-A, IGIBi003-A and IGIBi004-A)
Kumar D et al. Generation of three spinocerebellar ataxia type-12 patients derived induced pluripotent stem cell lines (IGIBi002-A, IGIBi003-A and IGIBi004-A). . 2018-08-00. Pubmed ID: 30130680; DOI: 10.1016/j.scr.2018.08.008 IGIBi002-AIGIBi003-AIGIBi004-A 2018-08-00 2018-08-00 PubMed: 30130680 DOI: 10.1016/j.scr.2018.08.008Associated cell lines:
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Devito L, Donne M, Kolundzic N, Khurana P, Hobbs C, Kaddour G, Dubrac S, Gruber R, Schmuth M, Mauro T, Ilic D
Induced pluripotent stem cell line from an atopic dermatitis patient heterozygous for c.2282del4 mutation in filaggrin: KCLi001-A
Devito L et al. Induced pluripotent stem cell line from an atopic dermatitis patient heterozygous for c.2282del4 mutation in filaggrin: KCLi001-A. . 2018-08-00. Pubmed ID: 30075366; DOI: 10.1016/j.scr.2018.07.014; PMC: PMC7514110 KCLi001-A 2018-08-00 2018-08-00 PubMed: 30075366 DOI: 10.1016/j.scr.2018.07.014Associated cell lines:
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Zhang X, Zhang D, Chen SC, Lamey T, Thompson JA, McLaren T, De Roach JN, Chen FK, McLenachan S
Establishment of an induced pluripotent stem cell line from a retinitis pigmentosa patient with compound heterozygous CRB1 mutation
Zhang X et al. Establishment of an induced pluripotent stem cell line from a retinitis pigmentosa patient with compound heterozygous CRB1 mutation. . 2018-08-00. Pubmed ID: 30092450; DOI: 10.1016/j.scr.2018.08.001 LEIi006-A 2018-08-00 2018-08-00 PubMed: 30092450 DOI: 10.1016/j.scr.2018.08.001Associated cell lines:
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Graffmann N, Bohndorf M, Ncube A, Wruck W, Kashofer K, Zatloukal K, Adjaye J
Establishment and characterization of an iPSC line from a 58 years old high grade patient with nonalcoholic fatty liver disease (70% steatosis) with homozygous wildtype PNPLA3 genotype
Graffmann N et al. Establishment and characterization of an iPSC line from a 58 years old high grade patient with nonalcoholic fatty liver disease (70% steatosis) with homozygous wildtype PNPLA3 genotype. . 2018-08-00. Pubmed ID: 30081348; DOI: 10.1016/j.scr.2018.07.011 HHUUKDi007-A 2018-08-00 2018-08-00 PubMed: 30081348 DOI: 10.1016/j.scr.2018.07.011Associated cell lines:
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Gagne AL, Maguire JA, Gandre-Babbe S, Chou ST, Tasian SK, Loh ML, Weiss MJ, Gadue P, French DL
Generation of a human Juvenile myelomonocytic leukemia iPSC line, CHOPi001-A, with a mutation in CBL
Gagne AL et al. Generation of a human Juvenile myelomonocytic leukemia iPSC line, CHOPi001-A, with a mutation in CBL. . 2018-08-00. Pubmed ID: 30096712; DOI: 10.1016/j.scr.2018.07.001; PMC: PMC7885123 CHOPi001-A 2018-08-00 2018-08-00 PubMed: 30096712 DOI: 10.1016/j.scr.2018.07.001Associated cell lines:
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Choi HY, Kim SJ, Go GY, Kwon A, Im YS, Ha HY, Hong JT, Jung JW, Koo SK
Generation of a human induced pluripotent stem cell line, KSCBi003-A, from human adipose tissue-derived mesenchymal stem cells using a chromosomal integration-free system
Choi HY et al. Generation of a human induced pluripotent stem cell line, KSCBi003-A, from human adipose tissue-derived mesenchymal stem cells using a chromosomal integration-free system. . 2018-08-00. Pubmed ID: 29979972; DOI: 10.1016/j.scr.2018.06.003 KSCBi003-A 2018-08-00 2018-08-00 PubMed: 29979972 DOI: 10.1016/j.scr.2018.06.003Associated cell lines:
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Boonkaew B, Tapeng L, Netsrithong R, Vatanashevanopakorn C, Pattanapanyasat K, Wattanapanitch M
Induced pluripotent stem cell line MUSIi006-A derived from hair follicle keratinocytes as a non-invasive somatic cell source
Boonkaew B et al. Induced pluripotent stem cell line MUSIi006-A derived from hair follicle keratinocytes as a non-invasive somatic cell source. . 2018-08-00. Pubmed ID: 30031234; DOI: 10.1016/j.scr.2018.07.007 MUSIi006-A 2018-08-00 2018-08-00 PubMed: 30031234 DOI: 10.1016/j.scr.2018.07.007Associated cell lines:
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Arioka Y, Kushima I, Mori D, Ozaki N
Three lines of induced pluripotent stem cells derived from a 15q11.2-q13.1 duplication syndrome patient
Arioka Y et al. Three lines of induced pluripotent stem cells derived from a 15q11.2-q13.1 duplication syndrome patient. . 2018-08-00. Pubmed ID: 30144654; DOI: 10.1016/j.scr.2018.08.004 PNUi002-APNUi002-BPNUi002-C 2018-08-00 2018-08-00 PubMed: 30144654 DOI: 10.1016/j.scr.2018.08.004 -
Trevisan M, Alvisi G, Barbaro V, Barzon L, Raffa P, Migliorati A, Desole G, Ruzittu S, Masi G, Di Iorio E, Palù G
Oral Mucosa-Derived Induced Pluripotent Stem Cells from Patients with Ectrodactyly-Ectodermal Dysplasia-Clefting Syndrome
Trevisan M et al. Oral Mucosa-Derived Induced Pluripotent Stem Cells from Patients with Ectrodactyly-Ectodermal Dysplasia-Clefting Syndrome. . 2018-08-00. Pubmed ID: 29989433; DOI: 10.1089/cell.2017.0064 UNIPDi001-AUNIPDi002-AUNIPDi003-A 2018-08-00 2018-08-00 PubMed: 29989433 DOI: 10.1089/cell.2017.0064Associated cell lines:
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Lee J, Woo DH, Park HJ, Ko DS, Kim JH
Generation of cytochrome P450 polymorphic human induced pluripotent stem cell lines with defective CYP activities
Lee J et al. Generation of cytochrome P450 polymorphic human induced pluripotent stem cell lines with defective CYP activities. . 2018-08-00. Pubmed ID: 30071395; DOI: 10.1016/j.scr.2018.07.010 LSCTRi002-ALSCTRi003-ALSCTRi004-A 2018-08-00 2018-08-00 PubMed: 30071395 DOI: 10.1016/j.scr.2018.07.010Associated cell lines:
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Nikitina TV, Menzorov AG, Kashevarova AA, Gridina MM, Khabarova AA, Yakovleva YS, Lopatkina ME, Kizilova EA, Vasilyev SA, Serov OL, Lebedev IN
Generation of two iPSC lines (IMGTi001-A and IMGTi001-B) from human skin fibroblasts with ring chromosome 22
Nikitina TV et al. Generation of two iPSC lines (IMGTi001-A and IMGTi001-B) from human skin fibroblasts with ring chromosome 22. . 2018-08-00. Pubmed ID: 30144655; DOI: 10.1016/j.scr.2018.08.012 IMGTi001-AIMGTi001-B 2018-08-00 2018-08-00 PubMed: 30144655 DOI: 10.1016/j.scr.2018.08.012Associated cell lines:
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Cárdenas A, Villalba A, de Juan Romero C, Picó E, Kyrousi C, Tzika AC, Tessier-Lavigne M, Ma L, Drukker M, Cappello S, Borrell V
Evolution of Cortical Neurogenesis in Amniotes Controlled by Robo Signaling Levels
Cárdenas A et al. Evolution of Cortical Neurogenesis in Amniotes Controlled by Robo Signaling Levels. . 2018-07-26. Pubmed ID: 29961574; DOI: 10.1016/j.cell.2018.06.007; PMC: PMC6063992 ISFi001-A 2018-07-26 2018-07-26 PubMed: 29961574 DOI: 10.1016/j.cell.2018.06.007Associated cell lines:
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Ramme Anja Patricia, Koenig Leopold, Hasenberg Tobias, Schwenk Christine, Magauer Corinna, Faust Daniel, Lorenz Alexandra K., Krebs Anna, Drewell Christopher, Schirrmann Kerstin, Vladetic Alexandra, Lin Grace-Chiaen, Pabinger Stephan, Neuhaus Winfried, Bois Frederic, Lauster Roland, Marx Uwe, Dehne Eva-Maria
Towards an autologous iPSC-derived patient-on-a-chip
Ramme Anja Patricia et al. Towards an autologous iPSC-derived patient-on-a-chip. . 2018-07-25. DOI: 10.1101/376970 TISSUi001-A 2018-07-25 2018-07-25 DOI: 10.1101/376970Associated cell lines:
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Coulter ME, Dorobantu CM, Lodewijk GA, Delalande F, Cianferani S, Ganesh VS, Smith RS, Lim ET, Xu CS, Pang S, Wong ET, Lidov HGW, Calicchio ML, Yang E, Gonzalez DM, Schlaeger TM, Mochida GH, Hess H, Lee WA, Lehtinen MK, Kirchhausen T, Haussler D, Jacobs FMJ, Gaudin R, Walsh CA
The ESCRT-III Protein CHMP1A Mediates Secretion of Sonic Hedgehog on a Distinctive Subtype of Extracellular Vesicles
Coulter ME et al. The ESCRT-III Protein CHMP1A Mediates Secretion of Sonic Hedgehog on a Distinctive Subtype of Extracellular Vesicles. . 2018-07-24. Pubmed ID: 30044992; DOI: 10.1016/j.celrep.2018.06.100; PMC: PMC6178983 WISCi004-B 2018-07-24 2018-07-24 PubMed: 30044992 DOI: 10.1016/j.celrep.2018.06.100Associated cell lines:
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Koyuncu S, Saez I, Lee HJ, Gutierrez-Garcia R, Pokrzywa W, Fatima A, Hoppe T, Vilchez D
The ubiquitin ligase UBR5 suppresses proteostasis collapse in pluripotent stem cells from Huntington's disease patients
Koyuncu S et al. The ubiquitin ligase UBR5 suppresses proteostasis collapse in pluripotent stem cells from Huntington's disease patients. . 2018-07-23. Pubmed ID: 30038412; DOI: 10.1038/s41467-018-05320-3; PMC: PMC6056416 UKBi003-AUKBi001-B 2018-07-23 2018-07-23 PubMed: 30038412 DOI: 10.1038/s41467-018-05320-3 -
MacAskill MG, Saif J, Condie A, Jansen MA, MacGillivray TJ, Tavares AAS, Fleisinger L, Spencer HL, Besnier M, Martin E, Biglino G, Newby DE, Hadoke PWF, Mountford JC, Emanueli C, Baker AH
Robust Revascularization in Models of Limb Ischemia Using a Clinically Translatable Human Stem Cell-Derived Endothelial Cell Product
MacAskill MG et al. Robust Revascularization in Models of Limb Ischemia Using a Clinically Translatable Human Stem Cell-Derived Endothelial Cell Product. . 2018-07-05. Pubmed ID: 29703701; DOI: 10.1016/j.ymthe.2018.03.017; PMC: PMC6035339 RCe021-A 2018-07-05 2018-07-05 PubMed: 29703701 DOI: 10.1016/j.ymthe.2018.03.017Associated cell lines:
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Lopez-Yrigoyen M, Fidanza A, Cassetta L, Axton RA, Taylor AH, Meseguer-Ripolles J, Tsakiridis A, Wilson V, Hay DC, Pollard JW, Forrester LM
A human iPSC line capable of differentiating into functional macrophages expressing ZsGreen: a tool for the study and in vivo tracking of therapeutic cells
Lopez-Yrigoyen M et al. A human iPSC line capable of differentiating into functional macrophages expressing ZsGreen: a tool for the study and in vivo tracking of therapeutic cells. . 2018-07-05. Pubmed ID: 29786554; DOI: 10.1098/rstb.2017.0219; PMC: PMC5974442 EDi020-A 2018-07-05 2018-07-05 PubMed: 29786554 DOI: 10.1098/rstb.2017.0219Associated cell lines:
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Rodriguez-Muela N, Parkhitko A, Grass T, Gibbs RM, Norabuena EM, Perrimon N, Singh R, Rubin LL
Blocking p62-dependent SMN degradation ameliorates spinal muscular atrophy disease phenotypes
Rodriguez-Muela N et al. Blocking p62-dependent SMN degradation ameliorates spinal muscular atrophy disease phenotypes. . 2018-07-02. Pubmed ID: 29672276; DOI: 10.1172/jci95231; PMC: PMC6025996 HVRDi005-AHVRDi015-AHVRDi016-AHVRDi017-A 2018-07-02 2018-07-02 PubMed: 29672276 DOI: 10.1172/jci95231Associated cell lines:
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Srinivasan G, Morgan D, Varun D, Brookhouser N, Brafman DA
An integrated biomanufacturing platform for the large-scale expansion and neuronal differentiation of human pluripotent stem cell-derived neural progenitor cells
Srinivasan G et al. An integrated biomanufacturing platform for the large-scale expansion and neuronal differentiation of human pluripotent stem cell-derived neural progenitor cells. . 2018-07-01. Pubmed ID: 29775730; DOI: 10.1016/j.actbio.2018.05.008; PMC: PMC8171278 ASUi003-AASUi004-A 2018-07-01 2018-07-01 PubMed: 29775730 DOI: 10.1016/j.actbio.2018.05.008 -
Hayer SN, Schelling Y, Hoeflinger P, Hauser S, Schöls L
Generation of an induced pluripotent stem cell line from a patient with adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP): HIHCNi003-A
Hayer SN et al. Generation of an induced pluripotent stem cell line from a patient with adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP): HIHCNi003-A. . 2018-07-00. Pubmed ID: 29980109; DOI: 10.1016/j.scr.2018.06.011 HIHCNi003-A 2018-07-00 2018-07-00 PubMed: 29980109 DOI: 10.1016/j.scr.2018.06.011Associated cell lines:
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Lehtonen Š, Höytyläinen I, Voutilainen J, Sonninen TM, Kuusisto J, Laakso M, Hämäläinen RH, Oksanen M, Koistinaho J
Generation of a human induced pluripotent stem cell line from a patient with a rare A673T variant in amyloid precursor protein gene that reduces the risk for Alzheimer's disease
Lehtonen Š et al. Generation of a human induced pluripotent stem cell line from a patient with a rare A673T variant in amyloid precursor protein gene that reduces the risk for Alzheimer's disease. . 2018-07-00. Pubmed ID: 29807259; DOI: 10.1016/j.scr.2018.05.014 UEFi001-A 2018-07-00 2018-07-00 PubMed: 29807259 DOI: 10.1016/j.scr.2018.05.014Associated cell lines:
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Chou SJ, Ko YL, Yang YH, Yarmishyn AA, Wu YT, Chen CT, Lee HC, Wei YH, Chiou SH
Generation of two isogenic human induced pluripotent stem cell lines from a 15 year-old female patient with MERRF syndrome and A8344G mutation of mitochondrial DNA
Chou SJ et al. Generation of two isogenic human induced pluripotent stem cell lines from a 15 year-old female patient with MERRF syndrome and A8344G mutation of mitochondrial DNA. . 2018-07-00. Pubmed ID: 29960149; DOI: 10.1016/j.scr.2018.05.011 TVGHi005-ATVGHi006-A 2018-07-00 2018-07-00 PubMed: 29960149 DOI: 10.1016/j.scr.2018.05.011Associated cell lines:
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Stelcer E, Kulcenty K, Rucinski M, Jopek K, Richter M, Trzeciak T, Suchorska WM
Chondrogenic differentiation in vitro of hiPSCs activates pathways engaged in limb development
Stelcer E et al. Chondrogenic differentiation in vitro of hiPSCs activates pathways engaged in limb development. . 2018-07-00. Pubmed ID: 29783101; DOI: 10.1016/j.scr.2018.05.006 GPCCi001-A 2018-07-00 2018-07-00 PubMed: 29783101 DOI: 10.1016/j.scr.2018.05.006Associated cell lines:
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Hayer SN, Schelling Y, Huebener-Schmid J, Weber JJ, Hauser S, Schöls L
Generation of an induced pluripotent stem cell line from a patient with spinocerebellar ataxia type 3 (SCA3): HIHCNi002-A
Hayer SN et al. Generation of an induced pluripotent stem cell line from a patient with spinocerebellar ataxia type 3 (SCA3): HIHCNi002-A. . 2018-07-00. Pubmed ID: 29936336; DOI: 10.1016/j.scr.2018.06.006 HIHCNi002-A 2018-07-00 2018-07-00 PubMed: 29936336 DOI: 10.1016/j.scr.2018.06.006Associated cell lines:
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Boonkaew B, Thummavichit W, Netsrithong R, Vatanashevanopakorn C, Pattanapanyasat K, Wattanapanitch M
Establishment of an integration-free induced pluripotent stem cell line (MUSIi005-A) from exfoliated renal epithelial cells
Boonkaew B et al. Establishment of an integration-free induced pluripotent stem cell line (MUSIi005-A) from exfoliated renal epithelial cells. . 2018-07-00. Pubmed ID: 29778975; DOI: 10.1016/j.scr.2018.05.002 MUSIi005-A 2018-07-00 2018-07-00 PubMed: 29778975 DOI: 10.1016/j.scr.2018.05.002Associated cell lines:
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Alari V, Russo S, Terragni B, Ajmone PF, Sironi A, Catusi I, Calzari L, Concolino D, Marotta R, Milani D, Giardino D, Mantegazza M, Gervasini C, Finelli P, Larizza L
iPSC-derived neurons of CREBBP- and EP300-mutated Rubinstein-Taybi syndrome patients show morphological alterations and hypoexcitability
Alari V et al. iPSC-derived neurons of CREBBP- and EP300-mutated Rubinstein-Taybi syndrome patients show morphological alterations and hypoexcitability. . 2018-07-00. Pubmed ID: 29883886; DOI: 10.1016/j.scr.2018.05.019 IAIi001-AIAIi002-AIAIi003-AIAIi004-A 2018-07-00 2018-07-00 PubMed: 29883886 DOI: 10.1016/j.scr.2018.05.019 -
Malysheva SV, Wunderlich S, Haase A, Göhring G, Martin U, Merkert S
Generation of a human CDX2 knock-in reporter iPSC line (MHHi007-A-1) to model human trophoblast differentiation
Malysheva SV et al. Generation of a human CDX2 knock-in reporter iPSC line (MHHi007-A-1) to model human trophoblast differentiation. . 2018-07-00. Pubmed ID: 29852468; DOI: 10.1016/j.scr.2018.05.015 MHHi007-AMHHi007-A-1 2018-07-00 2018-07-00 PubMed: 29852468 DOI: 10.1016/j.scr.2018.05.015Associated cell lines:
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Iyer S, Bhatia P, Rao M, Mukherjee O
Developing two reference control samples for the Indian population
Iyer S et al. Developing two reference control samples for the Indian population. . 2018-07-00. Pubmed ID: 29778976; DOI: 10.1016/j.scr.2018.05.001 ADBSi001-AADBSi002-A 2018-07-00 2018-07-00 PubMed: 29778976 DOI: 10.1016/j.scr.2018.05.001Associated cell lines:
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Ritthaphai A, Wattanapanitch M, Pithukpakorn M, Heepchantree W, Soi-Ampornkul R, Mahaisavariya P, Triwongwaranat D, Pattanapanyasat K, Vatanashevanopakorn C
Derivation of an induced pluripotent stem cell line (MUSIi004-A) from dermal fibroblasts of a 48-year-old spinocerebellar ataxia type 3 patient
Ritthaphai A et al. Derivation of an induced pluripotent stem cell line (MUSIi004-A) from dermal fibroblasts of a 48-year-old spinocerebellar ataxia type 3 patient. . 2018-07-00. Pubmed ID: 29852467; DOI: 10.1016/j.scr.2018.05.012 MUSIi004-A 2018-07-00 2018-07-00 PubMed: 29852467 DOI: 10.1016/j.scr.2018.05.012Associated cell lines:
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Lemoine MD, Krause T, Koivumäki JT, Prondzynski M, Schulze ML, Girdauskas E, Willems S, Hansen A, Eschenhagen T, Christ T
Human Induced Pluripotent Stem Cell-Derived Engineered Heart Tissue as a Sensitive Test System for QT Prolongation and Arrhythmic Triggers
Lemoine MD et al. Human Induced Pluripotent Stem Cell-Derived Engineered Heart Tissue as a Sensitive Test System for QT Prolongation and Arrhythmic Triggers. . 2018-07-00. Pubmed ID: 29925535; DOI: 10.1161/circep.117.006035 UKEi003-C 2018-07-00 2018-07-00 PubMed: 29925535 DOI: 10.1161/circep.117.006035Associated cell lines:
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Martins S, Yigit H, Bohndorf M, Graffmann N, Fiszl AR, Wruck W, Sleegers K, Van Broeckhoven C, Adjaye J
Lymphoblast-derived integration-free iPSC line AD-TREM2-3 from a 74 year-old Alzheimer's disease patient expressing the TREM2 p.R47H variant
Martins S et al. Lymphoblast-derived integration-free iPSC line AD-TREM2-3 from a 74 year-old Alzheimer's disease patient expressing the TREM2 p.R47H variant. . 2018-07-00. Pubmed ID: 29902745; DOI: 10.1016/j.scr.2018.05.018 HHUUKDi004-A 2018-07-00 2018-07-00 PubMed: 29902745 DOI: 10.1016/j.scr.2018.05.018Associated cell lines:
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Alari V, Russo S, Rovina D, Gowran A, Garzo M, Crippa M, Mazzanti L, Scalera C, Prosperi E, Giardino D, Gervasini C, Finelli P, Pompilio G, Larizza L
Generation of the Rubinstein-Taybi syndrome type 2 patient-derived induced pluripotent stem cell line (IAIi001-A) carrying the EP300 exon 23 stop mutation c.3829A > T, p.(Lys1277*)
Alari V et al. Generation of the Rubinstein-Taybi syndrome type 2 patient-derived induced pluripotent stem cell line (IAIi001-A) carrying the EP300 exon 23 stop mutation c.3829A > T, p.(Lys1277*). . 2018-07-00. Pubmed ID: 29944992; DOI: 10.1016/j.scr.2018.06.009 IAIi001-A 2018-07-00 2018-07-00 PubMed: 29944992 DOI: 10.1016/j.scr.2018.06.009Associated cell lines:
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Arioka Y, Kushima I, Kubo H, Mori D, Ozaki N
Induced pluripotent stem cells derived from a schizophrenia patient with ASTN2 deletion
Arioka Y et al. Induced pluripotent stem cells derived from a schizophrenia patient with ASTN2 deletion. . 2018-07-00. Pubmed ID: 29803967; DOI: 10.1016/j.scr.2018.05.013 PNUi001-B 2018-07-00 2018-07-00 PubMed: 29803967 DOI: 10.1016/j.scr.2018.05.013Associated cell lines:
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Cyganek L, Tiburcy M, Sekeres K, Gerstenberg K, Bohnenberger H, Lenz C, Henze S, Stauske M, Salinas G, Zimmermann WH, Hasenfuss G, Guan K
Deep phenotyping of human induced pluripotent stem cell-derived atrial and ventricular cardiomyocytes
Cyganek L et al. Deep phenotyping of human induced pluripotent stem cell-derived atrial and ventricular cardiomyocytes. . 2018-06-21. Pubmed ID: 29925689; DOI: 10.1172/jci.insight.99941; PMC: PMC6124434 UMGi001-AUMGi005-AUMGi014-A 2018-06-21 2018-06-21 PubMed: 29925689 DOI: 10.1172/jci.insight.99941 -
Juhola M, Joutsijoki H, Penttinen K, Aalto-Setälä K
Detection of genetic cardiac diseases by Ca(2+) transient profiles using machine learning methods
Juhola M et al. Detection of genetic cardiac diseases by Ca(2+) transient profiles using machine learning methods. . 2018-06-19. Pubmed ID: 29921843; DOI: 10.1038/s41598-018-27695-5; PMC: PMC6008430 TAUi006-BTAUi007-A 2018-06-19 2018-06-19 PubMed: 29921843 DOI: 10.1038/s41598-018-27695-5 -
Dorn T, Kornherr J, Parrotta EI, Zawada D, Ayetey H, Santamaria G, Iop L, Mastantuono E, Sinnecker D, Goedel A, Dirschinger RJ, My I, Laue S, Bozoglu T, Baarlink C, Ziegler T, Graf E, Hinkel R, Cuda G, Kääb S, Grace AA, Grosse R, Kupatt C, Meitinger T, Smith AG, Laugwitz KL, Moretti A
Interplay of cell-cell contacts and RhoA/MRTF-A signaling regulates cardiomyocyte identity
Dorn T et al. Interplay of cell-cell contacts and RhoA/MRTF-A signaling regulates cardiomyocyte identity. . 2018-06-15. Pubmed ID: 29764980; DOI: 10.15252/embj.201798133; PMC: PMC6003642 MRIi004-AMRIi013-AMRIi014-A 2018-06-15 2018-06-15 PubMed: 29764980 DOI: 10.15252/embj.201798133 -
Czerniecki SM, Cruz NM, Harder JL, Menon R, Annis J, Otto EA, Gulieva RE, Islas LV, Kim YK, Tran LM, Martins TJ, Pippin JW, Fu H, Kretzler M, Shankland SJ, Himmelfarb J, Moon RT, Paragas N, Freedman BS
High-Throughput Screening Enhances Kidney Organoid Differentiation from Human Pluripotent Stem Cells and Enables Automated Multidimensional Phenotyping
Czerniecki SM et al. High-Throughput Screening Enhances Kidney Organoid Differentiation from Human Pluripotent Stem Cells and Enables Automated Multidimensional Phenotyping. . 2018-06-01. Pubmed ID: 29779890; DOI: 10.1016/j.stem.2018.04.022; PMC: PMC5984728 WAe009-A 2018-06-01 2018-06-01 PubMed: 29779890 DOI: 10.1016/j.stem.2018.04.022Associated cell lines:
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El-Battrawy I, Zhao Z, Lan H, Cyganek L, Tombers C, Li X, Buljubasic F, Lang S, Tiburcy M, Zimmermann WH, Utikal J, Wieland T, Borggrefe M, Zhou XB, Akin I
Electrical dysfunctions in human-induced pluripotent stem cell-derived cardiomyocytes from a patient with an arrhythmogenic right ventricular cardiomyopathy
El-Battrawy I et al. Electrical dysfunctions in human-induced pluripotent stem cell-derived cardiomyocytes from a patient with an arrhythmogenic right ventricular cardiomyopathy. . 2018-06-01. Pubmed ID: 29566126; DOI: 10.1093/europace/euy042 UMGi121-AUMGi014-B 2018-06-01 2018-06-01 PubMed: 29566126 DOI: 10.1093/europace/euy042 -
André LM, Ausems CRM, Wansink DG, Wieringa B.
Abnormalities in Skeletal Muscle Myogenesis, Growth, and Regeneration in Myotonic Dystrophy.
André LM et al. Abnormalities in Skeletal Muscle Myogenesis, Growth, and Regeneration in Myotonic Dystrophy. . 2018-05-28. CHUQi001-A 2018-05-28 2018-05-28Associated cell lines:
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Vogt MA, Ehsaei Z, Knuckles P, Higginbottom A, Helmbrecht MS, Kunath T, Eggan K, Williams LA, Shaw PJ, Wurst W, Floss T, Huber AB, Taylor V
TDP-43 induces p53-mediated cell death of cortical progenitors and immature neurons
Vogt MA et al. TDP-43 induces p53-mediated cell death of cortical progenitors and immature neurons. . 2018-05-25. Pubmed ID: 29802307; DOI: 10.1038/s41598-018-26397-2; PMC: PMC5970242 HVRDi014-A 2018-05-25 2018-05-25 PubMed: 29802307 DOI: 10.1038/s41598-018-26397-2Associated cell lines:
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Matloka M, Klein AF, Rau F, Furling D.
Cells of Matter—In Vitro Models for Myotonic Dystrophy.
Matloka M et al. Cells of Matter—In Vitro Models for Myotonic Dystrophy. . 2018-05-23. CHUQi001-A 2018-05-23 2018-05-23Associated cell lines:
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Panova AV, Bogomazova AN, Lagarkova MA, Kiselev SL
Epigenetic reprogramming by naïve conditions establishes an irreversible state of partial X chromosome reactivation in female stem cells
Panova AV et al. Epigenetic reprogramming by naïve conditions establishes an irreversible state of partial X chromosome reactivation in female stem cells. . 2018-05-18. Pubmed ID: 29861859; DOI: 10.18632/oncotarget.25353; PMC: PMC5982739 HVRDe009-AWAe009-ARASe001-ARASe003-A 2018-05-18 2018-05-18 PubMed: 29861859 DOI: 10.18632/oncotarget.25353Associated cell lines:
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Olmer R, Engels L, Usman A, Menke S, Malik MNH, Pessler F, Göhring G, Bornhorst D, Bolten S, Abdelilah-Seyfried S, Scheper T, Kempf H, Zweigerdt R, Martin U
Differentiation of Human Pluripotent Stem Cells into Functional Endothelial Cells in Scalable Suspension Culture
Olmer R et al. Differentiation of Human Pluripotent Stem Cells into Functional Endothelial Cells in Scalable Suspension Culture. . 2018-05-08. Pubmed ID: 29681541; DOI: 10.1016/j.stemcr.2018.03.017; PMC: PMC5995343 MHHi001-AMHHi006-A 2018-05-08 2018-05-08 PubMed: 29681541 DOI: 10.1016/j.stemcr.2018.03.017 -
Halaidych OV, Freund C, van den Hil F, Salvatori DCF, Riminucci M, Mummery CL, Orlova VV
Inflammatory Responses and Barrier Function of Endothelial Cells Derived from Human Induced Pluripotent Stem Cells
Halaidych OV et al. Inflammatory Responses and Barrier Function of Endothelial Cells Derived from Human Induced Pluripotent Stem Cells. . 2018-05-08. Pubmed ID: 29657098; DOI: 10.1016/j.stemcr.2018.03.012; PMC: PMC5995303 LUMCi001-ALUMCi001-B 2018-05-08 2018-05-08 PubMed: 29657098 DOI: 10.1016/j.stemcr.2018.03.012Associated cell lines:
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Fleischer A, Lorenzo IM, Palomino E, Aasen T, Gómez F, Servera M, Asensio VJ, Gálvez V, Izpisúa-Belmonte JC, Bachiller D
Generation of two induced pluripotent stem cell (iPSC) lines from p.F508del Cystic Fibrosis patients
Fleischer A et al. Generation of two induced pluripotent stem cell (iPSC) lines from p.F508del Cystic Fibrosis patients. . 2018-05-00. Pubmed ID: 29554588; DOI: 10.1016/j.scr.2018.03.004 IMEDEAi001-AIMEDEAi001-BIMEDEAi001-CIMEDEAi001-DIMEDEAi001-EIMEDEAi001-FIMEDEAi001-GIMEDEAi002-AIMEDEAi002-BIMEDEAi003-A 2018-05-00 2018-05-00 PubMed: 29554588 DOI: 10.1016/j.scr.2018.03.004Associated cell lines:
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Sevilla A, Forero E, Zimmer M, Martinez H, Reggio K, Paull D, Egli D, Noggle S
Derivation and characterization of the NIH registry human stem cell line NYSCF100 line under defined feeder-free conditions
Sevilla A et al. Derivation and characterization of the NIH registry human stem cell line NYSCF100 line under defined feeder-free conditions. . 2018-05-00. Pubmed ID: 29631040; DOI: 10.1016/j.scr.2018.03.017 NYSCFe001-A 2018-05-00 2018-05-00 PubMed: 29631040 DOI: 10.1016/j.scr.2018.03.017Associated cell lines:
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Griscelli F, Ezanno H, Soubeyrand M, Feraud O, Oudrhiri N, Bonnefond A, Turhan AG, Froguel P, Bennaceur-Griscelli A
Generation of an induced pluripotent stem cell (iPSC) line from a patient with maturity-onset diabetes of the young type 3 (MODY3) carrying a hepatocyte nuclear factor 1-alpha (HNF1A) mutation
Griscelli F et al. Generation of an induced pluripotent stem cell (iPSC) line from a patient with maturity-onset diabetes of the young type 3 (MODY3) carrying a hepatocyte nuclear factor 1-alpha (HNF1A) mutation. . 2018-05-00. Pubmed ID: 29597128; DOI: 10.1016/j.scr.2018.02.017 UPSFRi013-A 2018-05-00 2018-05-00 PubMed: 29597128 DOI: 10.1016/j.scr.2018.02.017Associated cell lines:
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Gupta SK, Wesolowska-Andersen A, Ringgaard AK, Jaiswal H, Song L, Hastoy B, Ingvorsen C, Taheri-Ghahfarokhi A, Magnusson B, Maresca M, Jensen RR, Beer NL, Fels JJ, Grunnet LG, Thomas MK, Gloyn AL, Hicks R, McCarthy MI, Hansson M, Honoré C
NKX6.1 induced pluripotent stem cell reporter lines for isolation and analysis of functionally relevant neuronal and pancreas populations
Gupta SK et al. NKX6.1 induced pluripotent stem cell reporter lines for isolation and analysis of functionally relevant neuronal and pancreas populations. . 2018-05-00. Pubmed ID: 29734117; DOI: 10.1016/j.scr.2018.04.010 STBCi322-AUOXFi012-ASTBCi322-A-1 2018-05-00 2018-05-00 PubMed: 29734117 DOI: 10.1016/j.scr.2018.04.010Associated cell lines:
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Rotundo G, Bidollari E, Ferrari D, Spasari I, Bernardini L, Consoli F, De Luca A, Santimone I, Lamorte G, Migliore S, Squitieri F, Vescovi AL, Rosati J
Generation of the induced pluripotent stem cell line CSSi006-A (3681) from a patient affected by advanced-stage Juvenile Onset Huntington's Disease
Rotundo G et al. Generation of the induced pluripotent stem cell line CSSi006-A (3681) from a patient affected by advanced-stage Juvenile Onset Huntington's Disease. . 2018-05-00. Pubmed ID: 29704769; DOI: 10.1016/j.scr.2018.04.008 CSSi006-A 2018-05-00 2018-05-00 PubMed: 29704769 DOI: 10.1016/j.scr.2018.04.008Associated cell lines:
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Manian KV, Bharathan SP, Maddali M, Srivastava VM, Srivastava A, Velayudhan SR
Generation of an integration-free iPSC line (CSCRi005-A) from erythroid progenitor cells of a healthy Indian male individual
Manian KV et al. Generation of an integration-free iPSC line (CSCRi005-A) from erythroid progenitor cells of a healthy Indian male individual. . 2018-05-00. Pubmed ID: 29665501; DOI: 10.1016/j.scr.2018.03.020 CSCRi005-A 2018-05-00 2018-05-00 PubMed: 29665501 DOI: 10.1016/j.scr.2018.03.020Associated cell lines:
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Buijsen RAM, Gardiner SL, Bouma MJ, van der Graaf LM, Boogaard MW, Pepers BA, Eussen B, de Klein A, Freund C, van Roon-Mom WMC
Generation of 3 spinocerebellar ataxia type 1 (SCA1) patient-derived induced pluripotent stem cell lines LUMCi002-A, B, and C and 2 unaffected sibling control induced pluripotent stem cell lines LUMCi003-A and B
Buijsen RAM et al. Generation of 3 spinocerebellar ataxia type 1 (SCA1) patient-derived induced pluripotent stem cell lines LUMCi002-A, B, and C and 2 unaffected sibling control induced pluripotent stem cell lines LUMCi003-A and B. . 2018-05-00. Pubmed ID: 29656178; DOI: 10.1016/j.scr.2018.03.018 LUMCi002-ALUMCi003-ALUMCi002-BLUMCi002-CLUMCi003-B 2018-05-00 2018-05-00 PubMed: 29656178 DOI: 10.1016/j.scr.2018.03.018Associated cell lines:
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Sun H, Zhang F, Wang Y, Wang Z, Zhang S, Xu Y, Shi C
Generation of induced pluripotent stem cell line (ZZUi011-A) from urine sample of a normal human
Sun H et al. Generation of induced pluripotent stem cell line (ZZUi011-A) from urine sample of a normal human. . 2018-05-00. Pubmed ID: 29574173; DOI: 10.1016/j.scr.2018.03.002 ZZUi005-AZZUi009-AZZUi011-A 2018-05-00 2018-05-00 PubMed: 29574173 DOI: 10.1016/j.scr.2018.03.002 -
Sevilla A, Forero E, Zimmer M, Martinez H, Reggio K, Paull D, Egli D, Noggle S
Derivation and characterization of the NIH registry human stem cell line NYSCF101 under defined feeder-free conditions
Sevilla A et al. Derivation and characterization of the NIH registry human stem cell line NYSCF101 under defined feeder-free conditions. . 2018-05-00. Pubmed ID: 29730569; DOI: 10.1016/j.scr.2018.04.017 NYSCFe002-A 2018-05-00 2018-05-00 PubMed: 29730569 DOI: 10.1016/j.scr.2018.04.017Associated cell lines:
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Peng CH, Huang KC, Lu HE, Syu SH, Yarmishyn AA, Lu JF, Buddhakosai W, Lin TC, Hsu CC, Hwang DK, Shen CN, Chen SJ, Chiou SH
Generation of induced pluripotent stem cells from a patient with X-linked juvenile retinoschisis
Peng CH et al. Generation of induced pluripotent stem cells from a patient with X-linked juvenile retinoschisis. . 2018-05-00. Pubmed ID: 29674172; DOI: 10.1016/j.scr.2018.04.005 TVGHi003-A 2018-05-00 2018-05-00 PubMed: 29674172 DOI: 10.1016/j.scr.2018.04.005Associated cell lines:
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Hsu CC, Lu HE, Chuang JH, Ko YL, Tsai YC, Tai HY, Yarmishyn AA, Hwang DK, Wang ML, Yang YP, Chen SJ, Peng CH, Chiou SH, Lin TC
Generation of induced pluripotent stem cells from a patient with Best Dystrophy carrying 11q12.3 (BEST1 (VMD2)) mutation
Hsu CC et al. Generation of induced pluripotent stem cells from a patient with Best Dystrophy carrying 11q12.3 (BEST1 (VMD2)) mutation. . 2018-05-00. Pubmed ID: 29660606; DOI: 10.1016/j.scr.2018.03.019 TVGHi002-A 2018-05-00 2018-05-00 PubMed: 29660606 DOI: 10.1016/j.scr.2018.03.019Associated cell lines:
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Schuster S, Schelling Y, Synofzik M, Höflinger P, Schöls L, Hauser S
Establishment of STUB1/CHIP mutant induced pluripotent stem cells (iPSCs) from a patient with Gordon Holmes syndrome/SCAR16
Schuster S et al. Establishment of STUB1/CHIP mutant induced pluripotent stem cells (iPSCs) from a patient with Gordon Holmes syndrome/SCAR16. . 2018-05-00. Pubmed ID: 29679845; DOI: 10.1016/j.scr.2018.04.001 HIHCNi001-A 2018-05-00 2018-05-00 PubMed: 29679845 DOI: 10.1016/j.scr.2018.04.001Associated cell lines:
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Qi Z, Cui Y, Shi L, Luan J, Zhou X, Han J
Generation of urine-derived induced pluripotent stem cells from a patient with phenylketonuria
Qi Z et al. Generation of urine-derived induced pluripotent stem cells from a patient with phenylketonuria. . 2018-05-00. Pubmed ID: 29862149; DOI: 10.5582/irdr.2018.01032; PMC: PMC5982629 NJMUi001-A 2018-05-00 2018-05-00 PubMed: 29862149 DOI: 10.5582/irdr.2018.01032Associated cell lines:
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Liu Y, Wu F, Liu D, Wei R, Abbas N, Xia J, Li D, Wang H, Zhuang Y, Guo D, Chen Y, Wu Y, Ke X, Tao J, Yang F, Lai K, Shu X, Li YX
Generation of WAe001-A-15, a human embryonic stem cell line with miR-122 doxycycline-inducible expression
Liu Y et al. Generation of WAe001-A-15, a human embryonic stem cell line with miR-122 doxycycline-inducible expression. . 2018-05-00. Pubmed ID: 29627726; DOI: 10.1016/j.scr.2018.03.007 WAe001-AWAe001-A-15 2018-05-00 2018-05-00 PubMed: 29627726 DOI: 10.1016/j.scr.2018.03.007Associated cell lines:
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Eisen B, Ben Jehuda R, Cuttitta AJ, Mekies LN, Reiter I, Ramchandren S, Arad M, Michele DE, Binah O
Generation of Duchenne muscular dystrophy patient-specific induced pluripotent stem cell line lacking exons 45-50 of the dystrophin gene (IITi001-A)
Eisen B et al. Generation of Duchenne muscular dystrophy patient-specific induced pluripotent stem cell line lacking exons 45-50 of the dystrophin gene (IITi001-A). . 2018-05-00. Pubmed ID: 29653394; DOI: 10.1016/j.scr.2018.03.023; PMC: PMC5999581 IITi001-A 2018-05-00 2018-05-00 PubMed: 29653394 DOI: 10.1016/j.scr.2018.03.023Associated cell lines:
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Martins S, Yigit H, Bohndorf M, Graffmann N, Fiszl AR, Wruck W, Sleegers K, Van Broeckhoven C, Adjaye J
Lymphoblast-derived integration-free iPSC line AD-TREM2-1 from a 67year-old Alzheimer's disease patient expressing the TREM2 p.R47H variant
Martins S et al. Lymphoblast-derived integration-free iPSC line AD-TREM2-1 from a 67year-old Alzheimer's disease patient expressing the TREM2 p.R47H variant. . 2018-05-00. Pubmed ID: 29602048; DOI: 10.1016/j.scr.2018.03.011 HHUUKDi003-A 2018-05-00 2018-05-00 PubMed: 29602048 DOI: 10.1016/j.scr.2018.03.011Associated cell lines:
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Hansen M, Varga E, Aarts C, Wust T, Kuijpers T, von Lindern M, van den Akker E
Efficient production of erythroid, megakaryocytic and myeloid cells, using single cell-derived iPSC colony differentiation
Hansen M et al. Efficient production of erythroid, megakaryocytic and myeloid cells, using single cell-derived iPSC colony differentiation. . 2018-05-00. Pubmed ID: 29751281; DOI: 10.1016/j.scr.2018.04.016 SANi003-ASANi003-B 2018-05-00 2018-05-00 PubMed: 29751281 DOI: 10.1016/j.scr.2018.04.016 -
Vincent A, Khetan V, Rishi P, Suganeswari G, Krishnakumar S, Krishnan UM, Parameswaran S
Generation of a human induced pluripotent stem cell line (VRFi001-A) from orbital adipose tissue of a bilateral retinoblastoma patient with heterozygous RB1 gene deletion
Vincent A et al. Generation of a human induced pluripotent stem cell line (VRFi001-A) from orbital adipose tissue of a bilateral retinoblastoma patient with heterozygous RB1 gene deletion. . 2018-05-00. Pubmed ID: 29579639; DOI: 10.1016/j.scr.2018.03.012 VRFi001-A 2018-05-00 2018-05-00 PubMed: 29579639 DOI: 10.1016/j.scr.2018.03.012Associated cell lines:
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Guo Y, Zeng Q, Liu S, Yu Q, Wang P, Ma H, Shi S, Yan X, Cui Z, Xie M, Xue Y, Zha Q, Li Z, Zhang J, Tang S, Chen J
Generation of an iPS cell line via a non-integrative method using urine-derived cells from a patient with USH2A-associated retinitis pigmentosa
Guo Y et al. Generation of an iPS cell line via a non-integrative method using urine-derived cells from a patient with USH2A-associated retinitis pigmentosa. . 2018-05-00. Pubmed ID: 29660607; DOI: 10.1016/j.scr.2018.03.022 KLRMMEi001-A 2018-05-00 2018-05-00 PubMed: 29660607 DOI: 10.1016/j.scr.2018.03.022Associated cell lines:
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Peitz M, Bechler T, Thiele CC, Veltel M, Bloschies M, Fliessbach K, Ramirez A, Brüstle O
Blood-derived integration-free iPS cell line UKBi011-A from a diagnosed male Alzheimer's disease patient with APOE ɛ4/ɛ4 genotype
Peitz M et al. Blood-derived integration-free iPS cell line UKBi011-A from a diagnosed male Alzheimer's disease patient with APOE ɛ4/ɛ4 genotype. . 2018-05-00. Pubmed ID: 29753274; DOI: 10.1016/j.scr.2018.04.011 UKBi011-A 2018-05-00 2018-05-00 PubMed: 29753274 DOI: 10.1016/j.scr.2018.04.011Associated cell lines:
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Zhang X, Zhang D, Chen SC, Lamey T, Thompson JA, McLaren T, De Roach JN, Chen FK, McLenachan S
Generation of an induced pluripotent stem cell line from a patient with non-syndromic CLN3-associated retinal degeneration and a coisogenic control line
Zhang X et al. Generation of an induced pluripotent stem cell line from a patient with non-syndromic CLN3-associated retinal degeneration and a coisogenic control line. . 2018-05-00. Pubmed ID: 29753273; DOI: 10.1016/j.scr.2018.04.014 LEIi004-ALEIi004-A-1 2018-05-00 2018-05-00 PubMed: 29753273 DOI: 10.1016/j.scr.2018.04.014Associated cell lines:
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Zhang J, Wu S, Hu M, Liu Q
Generation of a human induced pluripotent stem cell line from urinary cells of a patient with primary congenital glaucoma using integration free Sendai technology
Zhang J et al. Generation of a human induced pluripotent stem cell line from urinary cells of a patient with primary congenital glaucoma using integration free Sendai technology. . 2018-05-00. Pubmed ID: 29677590; DOI: 10.1016/j.scr.2018.04.004 BIOi001-A 2018-05-00 2018-05-00 PubMed: 29677590 DOI: 10.1016/j.scr.2018.04.004Associated cell lines:
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Mura M, Ginevrino M, Zappatore R, Pisano F, Boni M, Castelletti S, Crotti L, Valente EM, Schwartz PJ, Gnecchi M
Generation of the human induced pluripotent stem cell (hiPSC) line PSMi003-A from a patient affected by an autosomal recessive form of Long QT Syndrome type 1
Mura M et al. Generation of the human induced pluripotent stem cell (hiPSC) line PSMi003-A from a patient affected by an autosomal recessive form of Long QT Syndrome type 1. . 2018-05-00. Pubmed ID: 29684900; DOI: 10.1016/j.scr.2018.04.003 PSMi003-A 2018-05-00 2018-05-00 PubMed: 29684900 DOI: 10.1016/j.scr.2018.04.003Associated cell lines:
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Mura M, Lee YK, Ginevrino M, Zappatore R, Pisano F, Boni M, Dagradi F, Crotti L, Valente EM, Schwartz PJ, Tse HF, Gnecchi M
Generation of the human induced pluripotent stem cell (hiPSC) line PSMi002-A from a patient affected by the Jervell and Lange-Nielsen syndrome and carrier of two compound heterozygous mutations on the KCNQ1 gene
Mura M et al. Generation of the human induced pluripotent stem cell (hiPSC) line PSMi002-A from a patient affected by the Jervell and Lange-Nielsen syndrome and carrier of two compound heterozygous mutations on the KCNQ1 gene. . 2018-05-00. Pubmed ID: 29677589; DOI: 10.1016/j.scr.2018.04.002 PSMi002-A 2018-05-00 2018-05-00 PubMed: 29677589 DOI: 10.1016/j.scr.2018.04.002Associated cell lines:
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Richard E, Brasil S, Briso-Montiano A, Alonso-Barroso E, Gallardo ME, Merinero B, Ugarte M, Desviat LR, Pérez B
Generation and characterization of two human iPSC lines from patients with methylmalonic acidemia cblB type
Richard E et al. Generation and characterization of two human iPSC lines from patients with methylmalonic acidemia cblB type. . 2018-05-00. Pubmed ID: 29660608; DOI: 10.1016/j.scr.2018.03.021 UAMi002-AUAMi003-A 2018-05-00 2018-05-00 PubMed: 29660608 DOI: 10.1016/j.scr.2018.03.021 -
Xu A, Zhou R, Tu J, Huo Z, Zhu D, Wang D, Gingold JA, Mata H, Rao PH, Liu M, Mohamed AMT, Kong CSL, Jewell BE, Xia W, Zhao R, Hung MC, Lee DF
Establishment of a human embryonic stem cell line with homozygous TP53 R248W mutant by TALEN mediated gene editing
Xu A et al. Establishment of a human embryonic stem cell line with homozygous TP53 R248W mutant by TALEN mediated gene editing. . 2018-05-00. Pubmed ID: 29730572; DOI: 10.1016/j.scr.2018.04.013; PMC: PMC6021017 WAe001-AWAe001-A-17 2018-05-00 2018-05-00 PubMed: 29730572 DOI: 10.1016/j.scr.2018.04.013Associated cell lines:
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Pars S, Cristo F, Inácio JM, Rosas G, Carreira IM, Melo JB, Mendes P, Martins DS, de Almeida LP, Maio J, Anjos R, Belo JA
Generation and characterization of a human iPS cell line from a patient-related control to study disease mechanisms associated with DAND5 p.R152H alteration
Pars S et al. Generation and characterization of a human iPS cell line from a patient-related control to study disease mechanisms associated with DAND5 p.R152H alteration. . 2018-05-00. Pubmed ID: 29730570; DOI: 10.1016/j.scr.2018.04.015 NMSUNLi001-A 2018-05-00 2018-05-00 PubMed: 29730570 DOI: 10.1016/j.scr.2018.04.015Associated cell lines:
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Sima N, Li R, Huang W, Xu M, Beers J, Zou J, Titus S, Ottinger EA, Marugan JJ, Xie X, Zheng W
Neural stem cells for disease modeling and evaluation of therapeutics for infantile (CLN1/PPT1) and late infantile (CLN2/TPP1) neuronal ceroid lipofuscinoses
Sima N et al. Neural stem cells for disease modeling and evaluation of therapeutics for infantile (CLN1/PPT1) and late infantile (CLN2/TPP1) neuronal ceroid lipofuscinoses. . 2018-04-10. Pubmed ID: 29631617; DOI: 10.1186/s13023-018-0798-2; PMC: PMC5891977 TRNDi027-ATRNDi028-A 2018-04-10 2018-04-10 PubMed: 29631617 DOI: 10.1186/s13023-018-0798-2Associated cell lines:
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Vögtle FN, Brändl B, Larson A, Pendziwiat M, Friederich MW, White SM, Basinger A, Kücükköse C, Muhle H, Jähn JA, Keminer O, Helbig KL, Delto CF, Myketin L, Mossmann D, Burger N, Miyake N, Burnett A, van Baalen A, Lovell MA, Matsumoto N, Walsh M, Yu HC, Shinde DN, Stephani U, Van Hove JLK, Müller FJ, Helbig I
Mutations in PMPCB Encoding the Catalytic Subunit of the Mitochondrial Presequence Protease Cause Neurodegeneration in Early Childhood
Vögtle FN et al. Mutations in PMPCB Encoding the Catalytic Subunit of the Mitochondrial Presequence Protease Cause Neurodegeneration in Early Childhood. . 2018-04-05. Pubmed ID: 29576218; DOI: 10.1016/j.ajhg.2018.02.014; PMC: PMC5985287 ZIPi013-A 2018-04-05 2018-04-05 PubMed: 29576218 DOI: 10.1016/j.ajhg.2018.02.014Associated cell lines:
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Duan X, Xie M, Peng Y, Hu L, Yu J, Zeng S, Wang Y, Lu G, Lin G, Sun Y
Generation of a human embryonic stem cell line expressing tetrameric Zoanthus sp. green fluorescent protein: NERCe002-A-1
Duan X et al. Generation of a human embryonic stem cell line expressing tetrameric Zoanthus sp. green fluorescent protein: NERCe002-A-1. . 2018-04-00. Pubmed ID: 29414419; DOI: 10.1016/j.scr.2018.01.033 NERCe002-ANERCe002-A-1 2018-04-00 2018-04-00 PubMed: 29414419 DOI: 10.1016/j.scr.2018.01.033Associated cell lines:
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Tu J, Huo Z, Liu M, Wang D, Xu A, Zhou R, Zhu D, Gingold J, Shen J, Zhao R, Lee DF
Generation of human embryonic stem cell line with heterozygous RB1 deletion by CRIPSR/Cas9 nickase
Tu J et al. Generation of human embryonic stem cell line with heterozygous RB1 deletion by CRIPSR/Cas9 nickase. . 2018-04-00. Pubmed ID: 29414415; DOI: 10.1016/j.scr.2018.01.021; PMC: PMC5905711 WAe001-A-19 2018-04-00 2018-04-00 PubMed: 29414415 DOI: 10.1016/j.scr.2018.01.021Associated cell lines:
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Sultanov R, Lebedeva O, Arapidi G, Lagarkova M, Kiselev S
Methylation profile of induced pluripotent stem cells generated by integration and integration-free approaches
Sultanov R et al. Methylation profile of induced pluripotent stem cells generated by integration and integration-free approaches. . 2018-04-00. Pubmed ID: 29552616; DOI: 10.1016/j.dib.2018.01.061; PMC: PMC5852269 RCPCMi009-A 2018-04-00 2018-04-00 PubMed: 29552616 DOI: 10.1016/j.dib.2018.01.061Associated cell lines:
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Maffioletti Sara Martina, Sarcar Shilpita, Henderson Alexander B.H., Mannhardt Ingra, Pinton Luca, Moyle Louise Anne, Steele-Stallard Heather, Cappellari Ornella, Wells Kim E., Ferrari Giulia, Mitchell Jamie S., Tyzack Giulia E., Kotiadis Vassilios N., Khedr Moustafa, Ragazzi Martina, Wang Weixin, Duchen Michael R., Patani Rickie, Zammit Peter S., Wells Dominic J., Eschenhagen Thomas, Tedesco Francesco Saverio
Three-Dimensional Human iPSC-Derived Artificial Skeletal Muscles Model Muscular Dystrophies and Enable Multilineage Tissue Engineering
Maffioletti Sara Martina et al. Three-Dimensional Human iPSC-Derived Artificial Skeletal Muscles Model Muscular Dystrophies and Enable Multilineage Tissue Engineering. . 2018-04-00. DOI: 10.1016/j.celrep.2018.03.091 CMDi001-ACMDi002-ACMDi003-ACMDi004-ACMDi005-A 2018-04-00 2018-04-00 DOI: 10.1016/j.celrep.2018.03.091 -
Guerra A, Musallam KM, Taher AT, Rivella S
Emerging Therapies
Guerra A et al. Emerging Therapies. . 2018-04-00. Pubmed ID: 29458736; DOI: 10.1016/j.hoc.2017.11.002; PMC: PMC5823282 MUi009-A 2018-04-00 2018-04-00 PubMed: 29458736 DOI: 10.1016/j.hoc.2017.11.002Associated cell lines:
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Song M, Ramakrishna S
Genome Editing in Stem Cells for Disease Therapeutics
Song M et al. Genome Editing in Stem Cells for Disease Therapeutics. . 2018-04-00. Pubmed ID: 29516417; DOI: 10.1007/s12033-018-0072-9 WAe001-AWAe001-A-14 2018-04-00 2018-04-00 PubMed: 29516417 DOI: 10.1007/s12033-018-0072-9Associated cell lines:
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Trevisan M, Di Iorio E, Masi G, Riccetti S, Barzon L, Alvisi G, Caenazzo L, Barbaro V, Palù G
Induced pluripotent stem cells line (UNIPDi003-A) from a patient affected by EEC syndrome carrying the R279H mutation in TP63 gene
Trevisan M et al. Induced pluripotent stem cells line (UNIPDi003-A) from a patient affected by EEC syndrome carrying the R279H mutation in TP63 gene. . 2018-04-00. Pubmed ID: 29477592; DOI: 10.1016/j.scr.2018.02.008 UNIPDi003-A 2018-04-00 2018-04-00 PubMed: 29477592 DOI: 10.1016/j.scr.2018.02.008Associated cell lines:
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Ortuño-Costela MDC, Moreno-Izquierdo A, Garesse R, Gallardo ME
Generation of a human iPSC line, IISHDOi002-A, with a 46, XY/47, XYY mosaicism and belonging to an African mitochondrial haplogroup
Ortuño-Costela MDC et al. Generation of a human iPSC line, IISHDOi002-A, with a 46, XY/47, XYY mosaicism and belonging to an African mitochondrial haplogroup. . 2018-04-00. Pubmed ID: 29471262; DOI: 10.1016/j.scr.2018.02.009 IISHDOi002-A 2018-04-00 2018-04-00 PubMed: 29471262 DOI: 10.1016/j.scr.2018.02.009Associated cell lines:
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Gao Y, Wilson GR, Bozaoglu K, Elefanty AG, Stanley EG, Dottori M, Lockhart PJ
Generation of RAB39B knockout isogenic human embryonic stem cell lines to model RAB39B-mediated Parkinson's disease
Gao Y et al. Generation of RAB39B knockout isogenic human embryonic stem cell lines to model RAB39B-mediated Parkinson's disease. . 2018-04-00. Pubmed ID: 29499499; DOI: 10.1016/j.scr.2018.02.015 SCSe001-ASCSe001-A-1SCSe001-A-2 2018-04-00 2018-04-00 PubMed: 29499499 DOI: 10.1016/j.scr.2018.02.015Associated cell lines:
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Gowran A, Spaltro G, Casalnuovo F, Vigorelli V, Spinelli P, Castiglioni E, Rovina D, Paganini S, Di Segni M, Gervasini C, Nigro P, Pompilio G
Generation of induced pluripotent stem cells from a Becker muscular dystrophy patient carrying a deletion of exons 45-55 of the dystrophin gene (CCMi002BMD-A-9 ∆45-55)
Gowran A et al. Generation of induced pluripotent stem cells from a Becker muscular dystrophy patient carrying a deletion of exons 45-55 of the dystrophin gene (CCMi002BMD-A-9 ∆45-55). . 2018-04-00. Pubmed ID: 29414413; DOI: 10.1016/j.scr.2018.01.025 CCMi002-A 2018-04-00 2018-04-00 PubMed: 29414413 DOI: 10.1016/j.scr.2018.01.025Associated cell lines:
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Peng Y, Xie M, Duan X, Hu L, Yu J, Zeng S, Wang Y, Ouyang Q, Lu G, Lin G, Sun Y
Generation of a luciferase-expressing human embryonic stem cell line: NERCe002-A-2
Peng Y et al. Generation of a luciferase-expressing human embryonic stem cell line: NERCe002-A-2. . 2018-04-00. Pubmed ID: 29501955; DOI: 10.1016/j.scr.2018.02.010 NERCe002-ANERCe002-A-2 2018-04-00 2018-04-00 PubMed: 29501955 DOI: 10.1016/j.scr.2018.02.010Associated cell lines:
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Bidollari E, Rotundo G, Ferrari D, Candido O, Bernardini L, Consoli F, De Luca A, Santimone I, Lamorte G, Ilari A, Squitieri F, Vescovi AL, Rosati J
Generation of induced pluripotent stem cell line, CSSi004-A (2962), from a patient diagnosed with Huntington's disease at the presymptomatic stage
Bidollari E et al. Generation of induced pluripotent stem cell line, CSSi004-A (2962), from a patient diagnosed with Huntington's disease at the presymptomatic stage. . 2018-04-00. Pubmed ID: 29486399; DOI: 10.1016/j.scr.2018.02.014 CSSi004-A 2018-04-00 2018-04-00 PubMed: 29486399 DOI: 10.1016/j.scr.2018.02.014Associated cell lines:
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Alvisi G, Trevisan M, Masi G, Canel V, Caenazzo L, Nespeca P, Barzon L, Di Iorio E, Barbaro V, Palù G
Generation of a transgene-free human induced pluripotent stem cell line (UNIPDi001-A) from oral mucosa epithelial stem cells
Alvisi G et al. Generation of a transgene-free human induced pluripotent stem cell line (UNIPDi001-A) from oral mucosa epithelial stem cells. . 2018-04-00. Pubmed ID: 29547871; DOI: 10.1016/j.scr.2018.02.007 UNIPDi001-A 2018-04-00 2018-04-00 PubMed: 29547871 DOI: 10.1016/j.scr.2018.02.007Associated cell lines:
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Wang Y, Shi C, Wang Z, Sun H, Yang Z, Zhang F, Liu Y, Liu H, Jiang C, Zhang S, Xu Y, Wen X
Generation of induced pluripotent stem cell line (ZZUi004-A) from urine sample of a patient with spinocerebellar ataxia type 3
Wang Y et al. Generation of induced pluripotent stem cell line (ZZUi004-A) from urine sample of a patient with spinocerebellar ataxia type 3. . 2018-04-00. Pubmed ID: 29444500; DOI: 10.1016/j.scr.2018.01.027 ZZUi004-A 2018-04-00 2018-04-00 PubMed: 29444500 DOI: 10.1016/j.scr.2018.01.027Associated cell lines:
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Artero Castro A, León M, Del Buey Furió V, Erceg S, Lukovic D
Generation of a human iPSC line by mRNA reprogramming
Artero Castro A et al. Generation of a human iPSC line by mRNA reprogramming. . 2018-04-00. Pubmed ID: 29499498; DOI: 10.1016/j.scr.2018.02.011 ESi062-A 2018-04-00 2018-04-00 PubMed: 29499498 DOI: 10.1016/j.scr.2018.02.011Associated cell lines:
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Marote A, Pomeshchik Y, Collin A, Goldwurm S, Lamas NJ, Pinto L, Salgado AJ, Roybon L
Generation of an induced pluripotent stem cell line (CSC-41) from a Parkinson's disease patient carrying a p.G2019S mutation in the LRRK2 gene
Marote A et al. Generation of an induced pluripotent stem cell line (CSC-41) from a Parkinson's disease patient carrying a p.G2019S mutation in the LRRK2 gene. . 2018-04-00. Pubmed ID: 29414418; DOI: 10.1016/j.scr.2018.01.022 ULUNDi002-A 2018-04-00 2018-04-00 PubMed: 29414418 DOI: 10.1016/j.scr.2018.01.022Associated cell lines:
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Altieri F, Turco EM, Vinci E, Torres B, Ferrari D, De Jaco A, Mazzoccoli G, Lamorte G, Nardone A, Della Monica M, Bernardini L, Vescovi AL, Rosati J
Production and characterization of CSSI003 (2961) human induced pluripotent stem cells (iPSCs) carrying a novel puntiform mutation in RAI1 gene, Causative of Smith-Magenis syndrome
Altieri F et al. Production and characterization of CSSI003 (2961) human induced pluripotent stem cells (iPSCs) carrying a novel puntiform mutation in RAI1 gene, Causative of Smith-Magenis syndrome. . 2018-04-00. Pubmed ID: 29494847; DOI: 10.1016/j.scr.2018.02.016 CSSi003-A 2018-04-00 2018-04-00 PubMed: 29494847 DOI: 10.1016/j.scr.2018.02.016Associated cell lines:
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He J, Duan X, Li W, Peng Y, Yu J, Hu L, Zeng S, Wang Y, Lu G, Lin G, Sun Y
Establishment and characterization of a human embryonic stem cell line, NERCe002-A-3, with inducible 14-3-3ζ overexpression
He J et al. Establishment and characterization of a human embryonic stem cell line, NERCe002-A-3, with inducible 14-3-3ζ overexpression. . 2018-04-00. Pubmed ID: 29414411; DOI: 10.1016/j.scr.2018.01.017 NERCe002-ANERCe002-A-3 2018-04-00 2018-04-00 PubMed: 29414411 DOI: 10.1016/j.scr.2018.01.017Associated cell lines:
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Wang Y, Yu J, Liu L, Li W, Duan X, Peng Y, Zeng S, Ouyang Q, Lu G, Lin G, Sun Y
Generation of a human embryonic stem cell line, NERCe003-A-1, with lentivirus vector-mediated inducible CTNNB1 overexpression
Wang Y et al. Generation of a human embryonic stem cell line, NERCe003-A-1, with lentivirus vector-mediated inducible CTNNB1 overexpression. . 2018-04-00. Pubmed ID: 29428849; DOI: 10.1016/j.scr.2018.01.020 NERCe003-ANERCe003-A-1 2018-04-00 2018-04-00 PubMed: 29428849 DOI: 10.1016/j.scr.2018.01.020Associated cell lines:
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Sarafian R, Morato-Marques M, Borsoi J, Pereira LV
Monitoring cell line identity in collections of human induced pluripotent stem cells
Sarafian R et al. Monitoring cell line identity in collections of human induced pluripotent stem cells. . 2018-04-00. Pubmed ID: 29433076; DOI: 10.1016/j.scr.2018.01.030 LANCEi007-ALANCEi009-ALANCEi014-ALANCEi015-ALANCEi016-ALANCEi017-ALANCEi018-ALANCEi020-ALANCEi029-A 2018-04-00 2018-04-00 PubMed: 29433076 DOI: 10.1016/j.scr.2018.01.030Associated cell lines:
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Cheng YC, Huang CY, Ho MC, Hsu YH, Syu SH, Lu HE, Lin HI, Lin CH, Hsieh PCH
Generation of 2 induced pluripotent stem cell lines derived from patients with Parkinson's disease carrying LRRK2 G2385R variant
Cheng YC et al. Generation of 2 induced pluripotent stem cell lines derived from patients with Parkinson's disease carrying LRRK2 G2385R variant. . 2018-04-00. Pubmed ID: 29414410; DOI: 10.1016/j.scr.2018.01.034 IBMSi007-AIBMSi008-A 2018-04-00 2018-04-00 PubMed: 29414410 DOI: 10.1016/j.scr.2018.01.034Associated cell lines:
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Jansch C, Günther K, Waider J, Ziegler GC, Forero A, Kollert S, Svirin E, Pühringer D, Kwok CK, Ullmann R, Maierhofer A, Flunkert J, Haaf T, Edenhofer F, Lesch KP
Generation of a human induced pluripotent stem cell (iPSC) line from a 51-year-old female with attention-deficit/hyperactivity disorder (ADHD) carrying a duplication of SLC2A3
Jansch C et al. Generation of a human induced pluripotent stem cell (iPSC) line from a 51-year-old female with attention-deficit/hyperactivity disorder (ADHD) carrying a duplication of SLC2A3. . 2018-04-00. Pubmed ID: 29477591; DOI: 10.1016/j.scr.2018.02.005 UKWi001-A 2018-04-00 2018-04-00 PubMed: 29477591 DOI: 10.1016/j.scr.2018.02.005Associated cell lines:
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Fernández-Susavila H, Mora C, Aramburu-Núñez M, Quintas-Rey R, Arias S, Collado M, López-Arias E, Sobrino T, Castillo J, Dell'Era P, Campos F
Generation and characterization of the human iPSC line IDISi001-A isolated from blood cells of a CADASIL patient carrying a NOTCH3 mutation
Fernández-Susavila H et al. Generation and characterization of the human iPSC line IDISi001-A isolated from blood cells of a CADASIL patient carrying a NOTCH3 mutation. . 2018-04-00. Pubmed ID: 29414412; DOI: 10.1016/j.scr.2018.01.023 IDISi001-A 2018-04-00 2018-04-00 PubMed: 29414412 DOI: 10.1016/j.scr.2018.01.023Associated cell lines:
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Bolinches-Amorós A, Lukovic D, Castro AA, León M, Kamenarova K, Kaneva R, Jendelova P, Blanco-Kelly F, Ayuso C, Cortón M, Erceg S
Generation of a human iPSC line from a patient with congenital glaucoma caused by mutation in CYP1B1 gene
Bolinches-Amorós A et al. Generation of a human iPSC line from a patient with congenital glaucoma caused by mutation in CYP1B1 gene. . 2018-04-00. Pubmed ID: 29453128; DOI: 10.1016/j.scr.2018.01.004 ESi047-A 2018-04-00 2018-04-00 PubMed: 29453128 DOI: 10.1016/j.scr.2018.01.004Associated cell lines:
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Liu SP, Hsu YH, Huang CY, Ho MC, Cheng YC, Wen CH, Lu HE, Tsai CH, Shyu WC, Hsieh PCH
Generation of novel induced pluripotent stem cell (iPSC) line from a 16-year-old sialidosis patient with NEU-1 gene mutation
Liu SP et al. Generation of novel induced pluripotent stem cell (iPSC) line from a 16-year-old sialidosis patient with NEU-1 gene mutation. . 2018-04-00. Pubmed ID: 29414417; DOI: 10.1016/j.scr.2018.01.024 IBMSi009-A 2018-04-00 2018-04-00 PubMed: 29414417 DOI: 10.1016/j.scr.2018.01.024Associated cell lines:
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Trevisan M, Barbaro V, Riccetti S, Masi G, Barzon L, Nespeca P, Alvisi G, Di Iorio E, Palù G
Generation of a transgene-free induced pluripotent stem cells line (UNIPDi002-A) from oral mucosa epithelial stem cells carrying the R304Q mutation in TP63 gene
Trevisan M et al. Generation of a transgene-free induced pluripotent stem cells line (UNIPDi002-A) from oral mucosa epithelial stem cells carrying the R304Q mutation in TP63 gene. . 2018-04-00. Pubmed ID: 29486400; DOI: 10.1016/j.scr.2018.02.006 UNIPDi002-A 2018-04-00 2018-04-00 PubMed: 29486400 DOI: 10.1016/j.scr.2018.02.006Associated cell lines:
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Tanaka Y, Sone T, Higurashi N, Sakuma T, Suzuki S, Ishikawa M, Yamamoto T, Mitsui J, Tsuji H, Okano H, Hirose S
Generation of D1-1 TALEN isogenic control cell line from Dravet syndrome patient iPSCs using TALEN-mediated editing of the SCN1A gene
Tanaka Y et al. Generation of D1-1 TALEN isogenic control cell line from Dravet syndrome patient iPSCs using TALEN-mediated editing of the SCN1A gene. . 2018-04-00. Pubmed ID: 29453127; DOI: 10.1016/j.scr.2018.01.036 FUi001-AFUi001-B 2018-04-00 2018-04-00 PubMed: 29453127 DOI: 10.1016/j.scr.2018.01.036 -
El-Battrawy I, Lan H, Cyganek L, Zhao Z, Li X, Buljubasic F, Lang S, Yücel G, Sattler K, Zimmermann WH, Utikal J, Wieland T, Ravens U, Borggrefe M, Zhou XB, Akin I
Modeling Short QT Syndrome Using Human-Induced Pluripotent Stem Cell-Derived Cardiomyocytes
El-Battrawy I et al. Modeling Short QT Syndrome Using Human-Induced Pluripotent Stem Cell-Derived Cardiomyocytes. . 2018-03-24. Pubmed ID: 29574456; DOI: 10.1161/jaha.117.007394; PMC: PMC5907581 UMGi120-AUMGi014-B 2018-03-24 2018-03-24 PubMed: 29574456 DOI: 10.1161/jaha.117.007394 -
van den Berg CW, Ritsma L, Avramut MC, Wiersma LE, van den Berg BM, Leuning DG, Lievers E, Koning M, Vanslambrouck JM, Koster AJ, Howden SE, Takasato M, Little MH, Rabelink TJ
Renal Subcapsular Transplantation of PSC-Derived Kidney Organoids Induces Neo-vasculogenesis and Significant Glomerular and Tubular Maturation In Vivo
van den Berg CW et al. Renal Subcapsular Transplantation of PSC-Derived Kidney Organoids Induces Neo-vasculogenesis and Significant Glomerular and Tubular Maturation In Vivo. . 2018-03-13. Pubmed ID: 29503086; DOI: 10.1016/j.stemcr.2018.01.041; PMC: PMC5918682 ESIBIe003-A-4LUMCi004-ALUMCi029-A 2018-03-13 2018-03-13 PubMed: 29503086 DOI: 10.1016/j.stemcr.2018.01.041Associated cell lines:
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Ulmer BM, Stoehr A, Schulze ML, Patel S, Gucek M, Mannhardt I, Funcke S, Murphy E, Eschenhagen T, Hansen A
Contractile Work Contributes to Maturation of Energy Metabolism in hiPSC-Derived Cardiomyocytes
Ulmer BM et al. Contractile Work Contributes to Maturation of Energy Metabolism in hiPSC-Derived Cardiomyocytes. . 2018-03-13. Pubmed ID: 29503093; DOI: 10.1016/j.stemcr.2018.01.039; PMC: PMC5919410 UKEi003-C 2018-03-13 2018-03-13 PubMed: 29503093 DOI: 10.1016/j.stemcr.2018.01.039Associated cell lines:
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Ferrer CM, Alders M, Postma AV, Park S, Klein MA, Cetinbas M, Pajkrt E, Glas A, van Koningsbruggen S, Christoffels VM, Mannens MMAM, Knegt L, Etchegaray JP, Sadreyev RI, Denu JM, Mostoslavsky G, van Maarle MC, Mostoslavsky R
An inactivating mutation in the histone deacetylase SIRT6 causes human perinatal lethality
Ferrer CM et al. An inactivating mutation in the histone deacetylase SIRT6 causes human perinatal lethality. . 2018-03-01. Pubmed ID: 29555651; DOI: 10.1101/gad.307330.117; PMC: PMC5900711 BUCREMi001-ABUCREMi002-A 2018-03-01 2018-03-01 PubMed: 29555651 DOI: 10.1101/gad.307330.117Associated cell lines:
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Chang CW, Chang CC, Hsia KC, Tsai SY
Generation of FHL2 homozygous knockout lines from human embryonic stem cells by CRISPR/Cas9-mediated ablation
Chang CW et al. Generation of FHL2 homozygous knockout lines from human embryonic stem cells by CRISPR/Cas9-mediated ablation. . 2018-03-00. Pubmed ID: 29291512; DOI: 10.1016/j.scr.2017.12.015 WAe009-A-8WAe009-A-9 2018-03-00 2018-03-00 PubMed: 29291512 DOI: 10.1016/j.scr.2017.12.015Associated cell lines:
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Lee J, Woo DH, Park HJ, Park K, Ko DS, Kim JH
Human induced pluripotent stem cell line with cytochrome P450 enzyme polymorphism (CYP2C19*2/CYP3A5*3C) generated from lymphoblastoid cells
Lee J et al. Human induced pluripotent stem cell line with cytochrome P450 enzyme polymorphism (CYP2C19*2/CYP3A5*3C) generated from lymphoblastoid cells. . 2018-03-00. Pubmed ID: 29310059; DOI: 10.1016/j.scr.2017.12.014 LSCTRi001-A 2018-03-00 2018-03-00 PubMed: 29310059 DOI: 10.1016/j.scr.2017.12.014Associated cell lines:
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Wu F, Gao G, Pan T, Yang Z, Xu G, Abbas N, Liu Y, Chen Y, Tan S, You K, Ke X, Zhuang Y, Lin X, Yang F, Li YX
Generation of a SMO homozygous knockout human embryonic stem cell line WAe001-A-16 by CRISPR/Cas9 editing
Wu F et al. Generation of a SMO homozygous knockout human embryonic stem cell line WAe001-A-16 by CRISPR/Cas9 editing. . 2018-03-00. Pubmed ID: 29278761; DOI: 10.1016/j.scr.2017.12.002 WAe001-AWAe001-A-16 2018-03-00 2018-03-00 PubMed: 29278761 DOI: 10.1016/j.scr.2017.12.002Associated cell lines:
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Fang F, Li Z, Zhao Q, Ye Z, Zhao K, Gu X, Shen S, Reijo Pera RA, Xiong C
Derivation of human induced pluripotent stem cell line (HUSTi001-A) from a 40-year-old patient with idiopathic infertility
Fang F et al. Derivation of human induced pluripotent stem cell line (HUSTi001-A) from a 40-year-old patient with idiopathic infertility. . 2018-03-00. Pubmed ID: 29414604; DOI: 10.1016/j.scr.2018.01.026 HUSTi001-A 2018-03-00 2018-03-00 PubMed: 29414604 DOI: 10.1016/j.scr.2018.01.026Associated cell lines:
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Wang Y, Yu H, Zhang Y, Zhang J, Chen K, Sun H, Meng S, Li G, Lei Y, Zhao J
Establishment of TUSMi003-A, an induced pluripotent stem cell (iPSC) line from a 62-year old Chinese Han patient with Alzheimer's disease with ApoE3/4 genetic background
Wang Y et al. Establishment of TUSMi003-A, an induced pluripotent stem cell (iPSC) line from a 62-year old Chinese Han patient with Alzheimer's disease with ApoE3/4 genetic background. . 2018-03-00. Pubmed ID: 29328972; DOI: 10.1016/j.scr.2018.01.005 TUSMi003-A 2018-03-00 2018-03-00 PubMed: 29328972 DOI: 10.1016/j.scr.2018.01.005Associated cell lines:
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Rim YA, Park N, Nam Y, Ham DS, Kim JW, Ha HY, Jung JW, Jung SM, Baek IC, Kim SY, Kim TG, Song J, Lee J, Park SH, Chung NG, Yoon KH, Ju JH
Recent progress of national banking project on homozygous HLA-typed induced pluripotent stem cells in South Korea
Rim YA et al. Recent progress of national banking project on homozygous HLA-typed induced pluripotent stem cells in South Korea. . 2018-03-00. Pubmed ID: 28941241; DOI: 10.1002/term.2578 KSCBi005-AKSCBi018-AKSCBi019-AKSCBi021-A 2018-03-00 2018-03-00 PubMed: 28941241 DOI: 10.1002/term.2578Associated cell lines:
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Marote A, Pomeshchik Y, Goldwurm S, Collin A, Lamas NJ, Pinto L, Salgado AJ, Roybon L
Generation of an induced pluripotent stem cell line (CSC-44) from a Parkinson's disease patient carrying a compound heterozygous mutation (c.823C>T and EX6 del) in the PARK2 gene
Marote A et al. Generation of an induced pluripotent stem cell line (CSC-44) from a Parkinson's disease patient carrying a compound heterozygous mutation (c.823C>T and EX6 del) in the PARK2 gene. . 2018-03-00. Pubmed ID: 29353703; DOI: 10.1016/j.scr.2018.01.006 ULUNDi006-A 2018-03-00 2018-03-00 PubMed: 29353703 DOI: 10.1016/j.scr.2018.01.006Associated cell lines:
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Correia C, Koshkin A, Duarte P, Hu D, Carido M, Sebastião MJ, Gomes-Alves P, Elliott DA, Domian IJ, Teixeira AP, Alves PM, Serra M
3D aggregate culture improves metabolic maturation of human pluripotent stem cell derived cardiomyocytes
Correia C et al. 3D aggregate culture improves metabolic maturation of human pluripotent stem cell derived cardiomyocytes. . 2018-03-00. Pubmed ID: 29178315; DOI: 10.1002/bit.26504 UKKi006-A 2018-03-00 2018-03-00 PubMed: 29178315 DOI: 10.1002/bit.26504Associated cell lines:
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Xu G, Guo D, Wu F, Abbas N, Lai K, Yuan F, You K, Liu Y, Zhuang Y, Wu Y, Xu Y, Chen Y, Yang F, Pan T, Li YX
Generation of a GDE heterozygous mutation human embryonic stem cell line WAe001-A-14 by CRISPR/Cas9 editing
Xu G et al. Generation of a GDE heterozygous mutation human embryonic stem cell line WAe001-A-14 by CRISPR/Cas9 editing. . 2018-03-00. Pubmed ID: 29310060; DOI: 10.1016/j.scr.2017.12.009 WAe001-AWAe001-A-14 2018-03-00 2018-03-00 PubMed: 29310060 DOI: 10.1016/j.scr.2017.12.009Associated cell lines:
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Wu YT, Hsu YH, Huang CY, Ho MC, Cheng YC, Wen CH, Ko HW, Lu HE, Chen YC, Tsai CL, Hsu YC, Wei YH, Hsieh PCH
Generation of an induced pluripotent stem cell (iPSC) line from a 40-year-old patient with the A8344G mutation of mitochondrial DNA and MERRF (myoclonic epilepsy with ragged red fibers) syndrome
Wu YT et al. Generation of an induced pluripotent stem cell (iPSC) line from a 40-year-old patient with the A8344G mutation of mitochondrial DNA and MERRF (myoclonic epilepsy with ragged red fibers) syndrome. . 2018-03-00. Pubmed ID: 29288969; DOI: 10.1016/j.scr.2017.12.013 IBMSi005-A 2018-03-00 2018-03-00 PubMed: 29288969 DOI: 10.1016/j.scr.2017.12.013Associated cell lines:
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Marote A, Pomeshchik Y, Goldwurm S, Collin A, Lamas NJ, Pinto L, Salgado AJ, Roybon L
Generation of an integration-free induced pluripotent stem cell line (CSC-43) from a patient with sporadic Parkinson's disease
Marote A et al. Generation of an integration-free induced pluripotent stem cell line (CSC-43) from a patient with sporadic Parkinson's disease. . 2018-03-00. Pubmed ID: 29334630; DOI: 10.1016/j.scr.2018.01.007 ULUNDi005-A 2018-03-00 2018-03-00 PubMed: 29334630 DOI: 10.1016/j.scr.2018.01.007Associated cell lines:
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Zhou R, Xu A, Wang D, Zhu D, Mata H, Huo Z, Tu J, Liu M, Mohamed AMT, Jewell BE, Gingold J, Xia W, Rao PH, Hung MC, Zhao R, Lee DF
A homozygous p53 R282W mutant human embryonic stem cell line generated using TALEN-mediated precise gene editing
Zhou R et al. A homozygous p53 R282W mutant human embryonic stem cell line generated using TALEN-mediated precise gene editing. . 2018-03-00. Pubmed ID: 29414603; DOI: 10.1016/j.scr.2018.01.035 WAe001-A-18 2018-03-00 2018-03-00 PubMed: 29414603 DOI: 10.1016/j.scr.2018.01.035Associated cell lines:
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Wang X, Sterr M, Burtscher I, Chen S, Hieronimus A, Machicao F, Staiger H, Häring HU, Lederer G, Meitinger T, Cernilogar FM, Schotta G, Irmler M, Beckers J, Hrabě de Angelis M, Ray M, Wright CVE, Bakhti M, Lickert H
Genome-wide analysis of PDX1 target genes in human pancreatic progenitors
Wang X et al. Genome-wide analysis of PDX1 target genes in human pancreatic progenitors. . 2018-03-00. Pubmed ID: 29396371; DOI: 10.1016/j.molmet.2018.01.011; PMC: PMC5870105 HMGUi001-A 2018-03-00 2018-03-00 PubMed: 29396371 DOI: 10.1016/j.molmet.2018.01.011Associated cell lines:
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Savchenko E, Marote A, Russ K, Collin A, Goldwurm S, Roybon L, Pomeshchik Y
Generation of a human induced pluripotent stem cell line (CSC-42) from a patient with sporadic form of Parkinson's disease
Savchenko E et al. Generation of a human induced pluripotent stem cell line (CSC-42) from a patient with sporadic form of Parkinson's disease. . 2018-03-00. Pubmed ID: 29334629; DOI: 10.1016/j.scr.2018.01.002 ULUNDi004-A 2018-03-00 2018-03-00 PubMed: 29334629 DOI: 10.1016/j.scr.2018.01.002Associated cell lines:
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Rosati J, Altieri F, Tardivo S, Turco EM, Goldoni M, Spasari I, Ferrari D, Bernardini L, Lamorte G, Valente EM, Vescovi AL
Production and characterization of human induced pluripotent stem cells (iPSCs) from Joubert Syndrome: CSSi001-A (2850)
Rosati J et al. Production and characterization of human induced pluripotent stem cells (iPSCs) from Joubert Syndrome: CSSi001-A (2850). . 2018-03-00. Pubmed ID: 29334628; DOI: 10.1016/j.scr.2018.01.012 CSSi001-A 2018-03-00 2018-03-00 PubMed: 29334628 DOI: 10.1016/j.scr.2018.01.012Associated cell lines:
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Wattanapanitch M, Ritthaphai A, Park C, Boonkaew B, Netsrithong R, Pattanapanyasat K, Limsiri P, Vatanashevanopakorn C
Generation of a human induced pluripotent stem cell line (MUSIi001-A) from caesarean section scar fibroblasts using Sendai viral vectors
Wattanapanitch M et al. Generation of a human induced pluripotent stem cell line (MUSIi001-A) from caesarean section scar fibroblasts using Sendai viral vectors. . 2018-03-00. Pubmed ID: 29367084; DOI: 10.1016/j.scr.2018.01.013 MUSIi001-A 2018-03-00 2018-03-00 PubMed: 29367084 DOI: 10.1016/j.scr.2018.01.013Associated cell lines:
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Wang Y, Jing N, Su L, Shi C, Zhang P, Wang Z, Sun H, Yang J, Liu Y, Wen X, Zhang J, Zhang S, Xu Y
Establishment of induced pluripotent stem cell line (ZZUi009-A) from an Alzheimer's disease patient carrying a PSEN1 gene mutation
Wang Y et al. Establishment of induced pluripotent stem cell line (ZZUi009-A) from an Alzheimer's disease patient carrying a PSEN1 gene mutation. . 2018-03-00. Pubmed ID: 29304399; DOI: 10.1016/j.scr.2017.12.005 ZZUi009-AZZUi037-A 2018-03-00 2018-03-00 PubMed: 29304399 DOI: 10.1016/j.scr.2017.12.005 -
Meraviglia V, Benzoni P, Landi S, Murano C, Langione M, Motta BM, Baratto S, Silipigni R, Di Segni M, Pramstaller PP, DiFrancesco D, Gazzerro E, Barbuti A, Rossini A
Generation of human induced pluripotent stem cells (EURACi001-A, EURACi002-A, EURACi003-A) from peripheral blood mononuclear cells of three patients carrying mutations in the CAV3 gene
Meraviglia V et al. Generation of human induced pluripotent stem cells (EURACi001-A, EURACi002-A, EURACi003-A) from peripheral blood mononuclear cells of three patients carrying mutations in the CAV3 gene. . 2018-03-00. Pubmed ID: 29304398; DOI: 10.1016/j.scr.2017.12.012 EURACi001-AEURACi002-AEURACi003-A 2018-03-00 2018-03-00 PubMed: 29304398 DOI: 10.1016/j.scr.2017.12.012Associated cell lines:
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Rosati J, Bidollari E, Rotundo G, Ferrari D, Torres B, Bernardini L, Consoli F, De Luca A, Santimone I, Lamorte G, Squitieri F, Vescovi AL
Generation of induced pluripotent stem cell line, CSSi002-A (2851), from a patient with juvenile Huntington Disease
Rosati J et al. Generation of induced pluripotent stem cell line, CSSi002-A (2851), from a patient with juvenile Huntington Disease. . 2018-03-00. Pubmed ID: 29342448; DOI: 10.1016/j.scr.2018.01.011 CSSi002-A 2018-03-00 2018-03-00 PubMed: 29342448 DOI: 10.1016/j.scr.2018.01.011Associated cell lines:
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Parveen S
Establishment and characterization of induced pluripotent stem cells from placental mesenchymal stromal cells
Parveen S. Establishment and characterization of induced pluripotent stem cells from placental mesenchymal stromal cells. . 2018-03-00. Pubmed ID: 29291511; DOI: 10.1016/j.scr.2017.12.008 SORMi001-A 2018-03-00 2018-03-00 PubMed: 29291511 DOI: 10.1016/j.scr.2017.12.008Associated cell lines:
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Fernandes S, Tembe S, Shinde P, Melinkeri S, Kale V, Limaye L
Establishment of human iPSC line NCCSi003-A from CD34(+)cells of peripheral blood collected during apheresis of healthy donor from Indian ethnicity
Fernandes S et al. Establishment of human iPSC line NCCSi003-A from CD34(+)cells of peripheral blood collected during apheresis of healthy donor from Indian ethnicity. . 2018-03-00. Pubmed ID: 29274886; DOI: 10.1016/j.scr.2017.12.011 NCCSi003-A 2018-03-00 2018-03-00 PubMed: 29274886 DOI: 10.1016/j.scr.2017.12.011Associated cell lines:
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Russ K, Marote A, Savchenko E, Collin A, Goldwurm S, Pomeshchik Y, Roybon L
Generation of a human induced pluripotent stem cell line (CSC-40) from a Parkinson's disease patient with a PINK1 p.Q456X mutation
Russ K et al. Generation of a human induced pluripotent stem cell line (CSC-40) from a Parkinson's disease patient with a PINK1 p.Q456X mutation. . 2018-03-00. Pubmed ID: 29331938; DOI: 10.1016/j.scr.2018.01.001 ULUNDi001-A 2018-03-00 2018-03-00 PubMed: 29331938 DOI: 10.1016/j.scr.2018.01.001Associated cell lines:
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Ogawa K, Suga H, Ozone C, Sakakibara M, Yamada T, Kano M, Mitsumoto K, Kasai T, Kodani Y, Nagasaki H, Yamamoto N, Hagiwara D, Goto M, Banno R, Sugimura Y, Arima H
Vasopressin-secreting neurons derived from human embryonic stem cells through specific induction of dorsal hypothalamic progenitors
Ogawa K et al. Vasopressin-secreting neurons derived from human embryonic stem cells through specific induction of dorsal hypothalamic progenitors. . 2018-02-26. Pubmed ID: 29483626; DOI: 10.1038/s41598-018-22053-x; PMC: PMC5827757 KUIMSe001-AKUIMSe003-A 2018-02-26 2018-02-26 PubMed: 29483626 DOI: 10.1038/s41598-018-22053-xAssociated cell lines:
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Stelcer E, Kulcenty K, Rucinski M, Jopek K, Trzeciak T, Richter M, Wroblewska JP, Suchorska WM
Expression of Pluripotency Genes in Chondrocyte-Like Cells Differentiated from Human Induced Pluripotent Stem Cells
Stelcer E et al. Expression of Pluripotency Genes in Chondrocyte-Like Cells Differentiated from Human Induced Pluripotent Stem Cells. . 2018-02-12. Pubmed ID: 29439516; DOI: 10.3390/ijms19020550; PMC: PMC5855772 GPCCi001-A 2018-02-12 2018-02-12 PubMed: 29439516 DOI: 10.3390/ijms19020550Associated cell lines:
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Böiers C, Richardson SE, Laycock E, Zriwil A, Turati VA, Brown J, Wray JP, Wang D, James C, Herrero J, Sitnicka E, Karlsson S, Smith AJH, Jacobsen SEW, Enver T
A Human IPS Model Implicates Embryonic B-Myeloid Fate Restriction as Developmental Susceptibility to B Acute Lymphoblastic Leukemia-Associated ETV6-RUNX1
Böiers C et al. A Human IPS Model Implicates Embryonic B-Myeloid Fate Restriction as Developmental Susceptibility to B Acute Lymphoblastic Leukemia-Associated ETV6-RUNX1. . 2018-02-05. Pubmed ID: 29290585; DOI: 10.1016/j.devcel.2017.12.005; PMC: PMC5807056 WAe001-AUOSi001-B 2018-02-05 2018-02-05 PubMed: 29290585 DOI: 10.1016/j.devcel.2017.12.005 -
Reuter Miriam S., Walker Susan, Thiruvahindrapuram Bhooma, Whitney Joe, Cohn Iris, Sondheimer Neal, Yuen Ryan K.C., Trost Brett, Paton Tara A., Pereira Sergio L., Herbrick Jo-Anne, Wintle Richard F., Merico Daniele, Howe Jennifer, MacDonald Jeffrey R., Lu Chao, Nalpathamkalam Thomas, Sung Wilson W.L., Wang Zhuozhi, Patel Rohan V., Pellecchia Giovanna, Wei John, Strug Lisa J., Bell Sherilyn, Kellam Barbara, Mahtani Melanie M., Bassett Anne S., Bombard Yvonne, Weksberg Rosanna, Shuman Cheryl, Cohn Ronald D., Stavropoulos Dimitri J., Bowdin Sarah, Hildebrandt Matthew R., Wei Wei, Romm Asli, Pasceri Peter, Ellis James, Ray Peter, Meyn M. Stephen, Monfared Nasim, Hosseini S. Mohsen, Joseph-George Ann M., Keeley Fred W., Cook Ryan A., Fiume Marc, Lee Hin C., Marshall Christian R., Davies Jill, Hazell Allison, Buchanan Janet A., Szego Michael J., Scherer Stephen W.
The Personal Genome Project Canada: findings from whole genome sequences of the inaugural 56 participants
Reuter Miriam S. et al. The Personal Genome Project Canada: findings from whole genome sequences of the inaugural 56 participants. . 2018-02-05. DOI: 10.1503/cmaj.171151 SKi001-A 2018-02-05 2018-02-05 DOI: 10.1503/cmaj.171151Associated cell lines:
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Phillips MJ, Capowski EE, Petersen A, Jansen AD, Barlow K, Edwards KL, Gamm DM
Generation of a rod-specific NRL reporter line in human pluripotent stem cells
Phillips MJ et al. Generation of a rod-specific NRL reporter line in human pluripotent stem cells. . 2018-02-05. Pubmed ID: 29402929; DOI: 10.1038/s41598-018-20813-3; PMC: PMC5799252 WAe009-A-R 2018-02-05 2018-02-05 PubMed: 29402929 DOI: 10.1038/s41598-018-20813-3Associated cell lines:
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Kwok CK, Ueda Y, Kadari A, Günther K, Ergün S, Heron A, Schnitzler AC, Rook M, Edenhofer F
Scalable stirred suspension culture for the generation of billions of human induced pluripotent stem cells using single-use bioreactors
Kwok CK et al. Scalable stirred suspension culture for the generation of billions of human induced pluripotent stem cells using single-use bioreactors. . 2018-02-00. Pubmed ID: 28382727; DOI: 10.1002/term.2435 JMUi001-A 2018-02-00 2018-02-00 PubMed: 28382727 DOI: 10.1002/term.2435Associated cell lines:
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Kunze C, Börner K, Kienle E, Orschmann T, Rusha E, Schneider M, Radivojkov-Blagojevic M, Drukker M, Desbordes S, Grimm D, Brack-Werner R
Synthetic AAV/CRISPR vectors for blocking HIV-1 expression in persistently infected astrocytes
Kunze C et al. Synthetic AAV/CRISPR vectors for blocking HIV-1 expression in persistently infected astrocytes. . 2018-02-00. Pubmed ID: 29119608; DOI: 10.1002/glia.23254 ISFi001-A 2018-02-00 2018-02-00 PubMed: 29119608 DOI: 10.1002/glia.23254Associated cell lines:
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Naaman H, Rabinski T, Yizhak A, Mizrahi S, Avni YS, Taube R, Rager B, Weinstein Y, Rall G, Gopas J, Ofir R
Measles Virus Persistent Infection of Human Induced Pluripotent Stem Cells
Naaman H et al. Measles Virus Persistent Infection of Human Induced Pluripotent Stem Cells. . 2018-02-00. Pubmed ID: 29412740; DOI: 10.1089/cell.2017.0034; PMC: PMC5804099 BGUi013-ABGUi014-A 2018-02-00 2018-02-00 PubMed: 29412740 DOI: 10.1089/cell.2017.0034 -
Achuta VS, Möykkynen T, Peteri UK, Turconi G, Rivera C, Keinänen K, Castrén ML
Functional changes of AMPA responses in human induced pluripotent stem cell-derived neural progenitors in fragile X syndrome
Achuta VS et al. Functional changes of AMPA responses in human induced pluripotent stem cell-derived neural progenitors in fragile X syndrome. . 2018-01-16. Pubmed ID: 29339535; DOI: 10.1126/scisignal.aan8784 ULBi003-AUHi007-B 2018-01-16 2018-01-16 PubMed: 29339535 DOI: 10.1126/scisignal.aan8784 -
Kurtz A, Seltmann S, Bairoch A, Bittner MS, Bruce K, Capes-Davis A, Clarke L, Crook JM, Daheron L, Dewender J, Faulconbridge A, Fujibuchi W, Gutteridge A, Hei DJ, Kim YO, Kim JH, Kokocinski AK, Lekschas F, Lomax GP, Loring JF, Ludwig T, Mah N, Matsui T, Müller R, Parkinson H, Sheldon M, Smith K, Stachelscheid H, Stacey G, Streeter I, Veiga A, Xu RH
A Standard Nomenclature for Referencing and Authentication of Pluripotent Stem Cells
Kurtz A et al. A Standard Nomenclature for Referencing and Authentication of Pluripotent Stem Cells. . 2018-01-09. Pubmed ID: 29320760; DOI: 10.1016/j.stemcr.2017.12.002; PMC: PMC5768986 WAe009-A 2018-01-09 2018-01-09 PubMed: 29320760 DOI: 10.1016/j.stemcr.2017.12.002Associated cell lines:
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Neehus AL, Lam J, Haake K, Merkert S, Schmidt N, Mucci A, Ackermann M, Schubert M, Happle C, Kühnel MP, Blank P, Philipp F, Goethe R, Jonigk D, Martin U, Kalinke U, Baumann U, Schambach A, Roesler J, Lachmann N
Impaired IFNγ-Signaling and Mycobacterial Clearance in IFNγR1-Deficient Human iPSC-Derived Macrophages
Neehus AL et al. Impaired IFNγ-Signaling and Mycobacterial Clearance in IFNγR1-Deficient Human iPSC-Derived Macrophages. . 2018-01-09. Pubmed ID: 29249666; DOI: 10.1016/j.stemcr.2017.11.011; PMC: PMC5768914 MHHi015-A 2018-01-09 2018-01-09 PubMed: 29249666 DOI: 10.1016/j.stemcr.2017.11.011Associated cell lines:
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Martineau L, Racine V, Benichou SA, Puymirat J
Lymphoblastoids cell lines - Derived iPSC line from a 26-year-old myotonic dystrophy type 1 patient carrying (CTG)(200) expansion in the DMPK gene: CHUQi001-A
Martineau L et al. Lymphoblastoids cell lines - Derived iPSC line from a 26-year-old myotonic dystrophy type 1 patient carrying (CTG)(200) expansion in the DMPK gene: CHUQi001-A. . 2018-01-00. Pubmed ID: 29274549; DOI: 10.1016/j.scr.2017.12.010 CHUQi001-A 2018-01-00 2018-01-00 PubMed: 29274549 DOI: 10.1016/j.scr.2017.12.010Associated cell lines:
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Vaňhara P, Kučera L, Prokeš L, Jurečková L, Peña-Méndez EM, Havel J, Hampl A
Intact Cell Mass Spectrometry as a Quality Control Tool for Revealing Minute Phenotypic Changes of Cultured Human Embryonic Stem Cells
Vaňhara P et al. Intact Cell Mass Spectrometry as a Quality Control Tool for Revealing Minute Phenotypic Changes of Cultured Human Embryonic Stem Cells. . 2018-01-00. Pubmed ID: 29248004; DOI: 10.1002/sctm.17-0107; PMC: PMC5746154 MUNIe007-A 2018-01-00 2018-01-00 PubMed: 29248004 DOI: 10.1002/sctm.17-0107Associated cell lines:
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Takada S, Kambe N, Kawasaki Y, Niwa A, Honda-Ozaki F, Kobayashi K, Osawa M, Nagahashi A, Semi K, Hotta A, Asaka I, Yamada Y, Nishikomori R, Heike T, Matsue H, Nakahata T, Saito MK
Pluripotent stem cell models of Blau syndrome reveal an IFN-γ-dependent inflammatory response in macrophages
Takada S et al. Pluripotent stem cell models of Blau syndrome reveal an IFN-γ-dependent inflammatory response in macrophages. . 2018-01-00. Pubmed ID: 28587749; DOI: 10.1016/j.jaci.2017.04.013 KUIFMSi004-C 2018-01-00 2018-01-00 PubMed: 28587749 DOI: 10.1016/j.jaci.2017.04.013Associated cell lines:
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Martins S, Bohndorf M, Schröter F, Assar F, Wruck W, Sleegers K, Van Broeckhoven C, Adjaye J
Lymphoblast-derived integration-free ISRM-CON9 iPS cell line from a 75year old female
Martins S et al. Lymphoblast-derived integration-free ISRM-CON9 iPS cell line from a 75year old female. . 2018-01-00. Pubmed ID: 29268155; DOI: 10.1016/j.scr.2017.12.007 HHUUKDi002-A 2018-01-00 2018-01-00 PubMed: 29268155 DOI: 10.1016/j.scr.2017.12.007Associated cell lines:
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Yuan F, Guo D, Liu Y, Xu Y, Gao G, Wu Y, Yang F, Ke X, Lai K, Wei H, Li YX
Generation of an ASS1 heterozygous knockout human embryonic stem cell line, WAe001-A-13, using CRISPR/Cas9
Yuan F et al. Generation of an ASS1 heterozygous knockout human embryonic stem cell line, WAe001-A-13, using CRISPR/Cas9. . 2018-01-00. Pubmed ID: 29247816; DOI: 10.1016/j.scr.2017.11.007 WAe001-AWAe001-A-13 2018-01-00 2018-01-00 PubMed: 29247816 DOI: 10.1016/j.scr.2017.11.007Associated cell lines:
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Dejosez M, Zwaka TP
Generation of hiPSTZ16 (ISMMSi003-A) cell line from normal human foreskin fibroblasts
Dejosez M et al. Generation of hiPSTZ16 (ISMMSi003-A) cell line from normal human foreskin fibroblasts. . 2018-01-00. Pubmed ID: 29227831; DOI: 10.1016/j.scr.2017.11.019 ISMMSi003-A 2018-01-00 2018-01-00 PubMed: 29227831 DOI: 10.1016/j.scr.2017.11.019Associated cell lines:
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Kim H, Kim JW, Kim SJ, Choi YJ, Kim DS, Park HJ
Generation of a PXR reporter human induced pluripotent stem cell line (PXR-mCherry hiPSC) using the CRISPR/Cas9 system
Kim H et al. Generation of a PXR reporter human induced pluripotent stem cell line (PXR-mCherry hiPSC) using the CRISPR/Cas9 system. . 2018-01-00. Pubmed ID: 29247817; DOI: 10.1016/j.scr.2017.12.001 KITi001-A 2018-01-00 2018-01-00 PubMed: 29247817 DOI: 10.1016/j.scr.2017.12.001Associated cell lines:
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Fernandes S, Shinde P, Khan N, Singh S, Vardhan S, Nair V, Kale V, Limaye L
Derivation of human iPSC line NCCSi002-A from umbilical cord blood (UCB) CD34+cells of donor from Indian ethnicity
Fernandes S et al. Derivation of human iPSC line NCCSi002-A from umbilical cord blood (UCB) CD34+cells of donor from Indian ethnicity. . 2018-01-00. Pubmed ID: 29268156; DOI: 10.1016/j.scr.2017.12.006 NCCSi002-A 2018-01-00 2018-01-00 PubMed: 29268156 DOI: 10.1016/j.scr.2017.12.006Associated cell lines:
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Ahola A, Pölönen RP, Aalto-Setälä K, Hyttinen J
Simultaneous Measurement of Contraction and Calcium Transients in Stem Cell Derived Cardiomyocytes
Ahola A et al. Simultaneous Measurement of Contraction and Calcium Transients in Stem Cell Derived Cardiomyocytes. . 2018-01-00. Pubmed ID: 28975460; DOI: 10.1007/s10439-017-1933-2; PMC: PMC5754453 TAUi002-A 2018-01-00 2018-01-00 PubMed: 28975460 DOI: 10.1007/s10439-017-1933-2Associated cell lines:
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Ben M'Barek K, Habeler W, Plancheron A, Jarraya M, Regent F, Terray A, Yang Y, Chatrousse L, Domingues S, Masson Y, Sahel JA, Peschanski M, Goureau O, Monville C
Human ESC-derived retinal epithelial cell sheets potentiate rescue of photoreceptor cell loss in rats with retinal degeneration
Ben M'Barek K et al. Human ESC-derived retinal epithelial cell sheets potentiate rescue of photoreceptor cell loss in rats with retinal degeneration. . 2017-12-20. Pubmed ID: 29263231; DOI: 10.1126/scitranslmed.aai7471 RCe013-A 2017-12-20 2017-12-20 PubMed: 29263231 DOI: 10.1126/scitranslmed.aai7471Associated cell lines:
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Buskin Adriana, Zhu Lili, Chichagova Valeria, Basu Basudha, Mozaffari-Jovin Sina, Dolan David, Droop Alastair, Collin Joseph, Bronstein Revital, Mehrotra Sudeep, Farkas Michael, Hilgen Gerrit, White Kathryn, Hallam Dean, Bialas Katarzyna, Chung Git, Mellough Carla, Ding Yuchun, Krasnogor Natalio, Przyborski Stefan, Al-Aama Jumana, Alharthi Sameer, Xu Yaobo, Wheway Gabrielle, Szymanska Katarzyna, McKibbin Martin, Inglehearn Chris F, Elliott David J, Lindsay Susan, Ali Robin R, Steel David H, Armstrong Lyle, Sernagor Evelyne, Pierce Eric, Lüehrmann Reinhard, Grellscheid Sushma-Nagaraja, Johnson Colin A, Lako Majlinda
Human iPSC-derived RPE and retinal organoids reveal impaired alternative splicing of genes involved in pre-mRNA splicing in PRPF31 autosomal dominant retinitis pigmentosa
Buskin Adriana et al. Human iPSC-derived RPE and retinal organoids reveal impaired alternative splicing of genes involved in pre-mRNA splicing in PRPF31 autosomal dominant retinitis pigmentosa. . 2017-12-11. DOI: 10.1101/232397 UNEWi001-AUNEWi004-AUNEWi005-A 2017-12-11 2017-12-11 DOI: 10.1101/232397Associated cell lines:
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Stelcer E, Kulcenty K, Suchorska WM
Chondrocytes differentiated from human induced pluripotent stem cells: Response to ionizing radiation
Stelcer E et al. Chondrocytes differentiated from human induced pluripotent stem cells: Response to ionizing radiation. . 2018-00-00. Pubmed ID: 30352062; DOI: 10.1371/journal.pone.0205691; PMC: PMC6198947 GPCCi001-A 2018-00-00 2018-00-00 PubMed: 30352062 DOI: 10.1371/journal.pone.0205691Associated cell lines:
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Spaltro G, Vigorelli V, Casalnuovo F, Spinelli P, Castiglioni E, Rovina D, Paganini S, Di Segni M, Nigro P, Gervasini C, Pompilio G, Gowran A
Derivation of the Duchenne muscular dystrophy patient-derived induced pluripotent stem cell line lacking DMD exons 49 and 50 (CCMi001DMD-A-3, ∆49, ∆50)
Spaltro G et al. Derivation of the Duchenne muscular dystrophy patient-derived induced pluripotent stem cell line lacking DMD exons 49 and 50 (CCMi001DMD-A-3, ∆49, ∆50). . 2017-12-00. Pubmed ID: 29127875; DOI: 10.1016/j.scr.2017.10.018 CCMi001-A 2017-12-00 2017-12-00 PubMed: 29127875 DOI: 10.1016/j.scr.2017.10.018Associated cell lines:
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Varga E, Hansen M, Wüst T, von Lindern M, van den Akker E
Generation of human erythroblast-derived iPSC line using episomal reprogramming system
Varga E et al. Generation of human erythroblast-derived iPSC line using episomal reprogramming system. . 2017-12-00. Pubmed ID: 29040913; DOI: 10.1016/j.scr.2017.10.001 SANi003-A 2017-12-00 2017-12-00 PubMed: 29040913 DOI: 10.1016/j.scr.2017.10.001Associated cell lines:
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Domingo-Reines J, López-Ornelas A, Montes R, Romero T, Rodriguez-Llamas JL, Lara-Rodarte R, González-Pozas F, Ayllon V, Menendez P, Velasco I, Ramos-Mejia V
Hoxa9 and EGFP reporter expression in human Embryonic Stem Cells (hESC) as useful tools for studying human development
Domingo-Reines J et al. Hoxa9 and EGFP reporter expression in human Embryonic Stem Cells (hESC) as useful tools for studying human development. . 2017-12-00. Pubmed ID: 29246576; DOI: 10.1016/j.scr.2017.08.004 WAe009-AWAe009-A-4WAe009-A-7 2017-12-00 2017-12-00 PubMed: 29246576 DOI: 10.1016/j.scr.2017.08.004Associated cell lines:
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Schick R, Mekies LN, Shemer Y, Eisen B, Hallas T, Ben Jehuda R, Ben-Ari M, Szantai A, Willi L, Shulman R, Gramlich M, Pane LS, My I, Freimark D, Murgia M, Santamaria G, Gherghiceanu M, Arad M, Moretti A, Binah O
Functional abnormalities in induced Pluripotent Stem Cell-derived cardiomyocytes generated from titin-mutated patients with dilated cardiomyopathy
Schick R et al. Functional abnormalities in induced Pluripotent Stem Cell-derived cardiomyocytes generated from titin-mutated patients with dilated cardiomyopathy. . 2018-00-00. Pubmed ID: 30332462; DOI: 10.1371/journal.pone.0205719; PMC: PMC6192629 IITi001-A 2018-00-00 2018-00-00 PubMed: 30332462 DOI: 10.1371/journal.pone.0205719Associated cell lines:
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Xu T, Liang D, Zhang J, Ji X, Hu H, Sun Y, Jiang T, Wang X, Hu P, Xu Z
Generation of integration-free induced pluripotent stem cell line (NJMUi001-A) from a phenylketonuria patient
Xu T et al. Generation of integration-free induced pluripotent stem cell line (NJMUi001-A) from a phenylketonuria patient. . 2017-12-00. Pubmed ID: 29154227; DOI: 10.1016/j.scr.2017.11.008 NJMUi001-A 2017-12-00 2017-12-00 PubMed: 29154227 DOI: 10.1016/j.scr.2017.11.008Associated cell lines:
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Bohndorf M, Ncube A, Spitzhorn LS, Enczmann J, Wruck W, Adjaye J
Derivation and characterization of integration-free iPSC line ISRM-UM51 derived from SIX2-positive renal cells isolated from urine of an African male expressing the CYP2D6 *4/*17 variant which confers intermediate drug metabolizing activity
Bohndorf M et al. Derivation and characterization of integration-free iPSC line ISRM-UM51 derived from SIX2-positive renal cells isolated from urine of an African male expressing the CYP2D6 *4/*17 variant which confers intermediate drug metabolizing activity. . 2017-12-00. Pubmed ID: 29035842; DOI: 10.1016/j.scr.2017.10.004 HHUUKDi001-A 2017-12-00 2017-12-00 PubMed: 29035842 DOI: 10.1016/j.scr.2017.10.004Associated cell lines:
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Kuebler B, Aran B, Miquel-Serra L, Muñoz Y, Ars E, Bullich G, Furlano M, Torra R, Marti M, Veiga A, Raya A
Generation of integration-free induced pluripotent stem cell lines derived from two patients with X-linked Alport syndrome (XLAS)
Kuebler B et al. Generation of integration-free induced pluripotent stem cell lines derived from two patients with X-linked Alport syndrome (XLAS). . 2017-12-00. Pubmed ID: 29150092; DOI: 10.1016/j.scr.2017.08.019 ESi055-AESi056-A 2017-12-00 2017-12-00 PubMed: 29150092 DOI: 10.1016/j.scr.2017.08.019 -
Stelcer E, Kulcenty K, Rucinski M, Jopek K, Richter M, Trzeciak T, Suchorska WM
Forced differentiation in vitro leads to stress-induced activation of DNA damage response in hiPSC-derived chondrocyte-like cells
Stelcer E et al. Forced differentiation in vitro leads to stress-induced activation of DNA damage response in hiPSC-derived chondrocyte-like cells. . 2018-00-00. Pubmed ID: 29864138; DOI: 10.1371/journal.pone.0198079; PMC: PMC5986142 GPCCi001-A 2018-00-00 2018-00-00 PubMed: 29864138 DOI: 10.1371/journal.pone.0198079Associated cell lines:
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Kuebler B, Aran B, Miquel-Serra L, Muñoz Y, Ars E, Bullich G, Furlano M, Torra R, Marti M, Veiga A, Raya A
Integration-free induced pluripotent stem cells derived from a patient with autosomal recessive Alport syndrome (ARAS)
Kuebler B et al. Integration-free induced pluripotent stem cells derived from a patient with autosomal recessive Alport syndrome (ARAS). . 2017-12-00. Pubmed ID: 29246570; DOI: 10.1016/j.scr.2017.08.021 ESi054-A 2017-12-00 2017-12-00 PubMed: 29246570 DOI: 10.1016/j.scr.2017.08.021Associated cell lines:
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Rauch C, Feifel E, Kern G, Murphy C, Meier F, Parson W, Beilmann M, Jennings P, Gstraunthaler G, Wilmes A
Differentiation of human iPSCs into functional podocytes
Rauch C et al. Differentiation of human iPSCs into functional podocytes. . 2018-00-00. Pubmed ID: 30222766; DOI: 10.1371/journal.pone.0203869; PMC: PMC6141081 STBCi028-ASTBCi321-ASTBCi322-AUOXFi012-A 2018-00-00 2018-00-00 PubMed: 30222766 DOI: 10.1371/journal.pone.0203869Associated cell lines:
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Wang Z, Zhang P, Wang Y, Shi C, Jing N, Sun H, Yang J, Liu Y, Wen X, Zhang J, Zhang S, Xu Y
Establishment of induced pluripotent stem cell line (ZZUi010-A) from an Alzheimer's disease patient carrying an APP gene mutation
Wang Z et al. Establishment of induced pluripotent stem cell line (ZZUi010-A) from an Alzheimer's disease patient carrying an APP gene mutation. . 2017-12-00. Pubmed ID: 29156377; DOI: 10.1016/j.scr.2017.10.025 ZZUi010-A 2017-12-00 2017-12-00 PubMed: 29156377 DOI: 10.1016/j.scr.2017.10.025Associated cell lines:
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Terray A, Fort V, Slembrouck A, Nanteau C, Sahel JA, Reichman S, Audo I, Goureau O
Establishment of an induced pluripotent stem (iPS) cell line from dermal fibroblasts of an asymptomatic patient with dominant PRPF31 mutation
Terray A et al. Establishment of an induced pluripotent stem (iPS) cell line from dermal fibroblasts of an asymptomatic patient with dominant PRPF31 mutation. . 2017-12-00. Pubmed ID: 29040912; DOI: 10.1016/j.scr.2017.10.007 IDVi002-A 2017-12-00 2017-12-00 PubMed: 29040912 DOI: 10.1016/j.scr.2017.10.007Associated cell lines:
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Son D, Quan Z, Kang PJ, Park G, Kang HC, You S
Generation of two induced pluripotent stem cell (iPSC) lines from X-linked adrenoleukodystrophy (X-ALD) patients with adrenomyeloneuropathy (AMN)
Son D et al. Generation of two induced pluripotent stem cell (iPSC) lines from X-linked adrenoleukodystrophy (X-ALD) patients with adrenomyeloneuropathy (AMN). . 2017-12-00. Pubmed ID: 29065337; DOI: 10.1016/j.scr.2017.10.003 SCHi001-A 2017-12-00 2017-12-00 PubMed: 29065337 DOI: 10.1016/j.scr.2017.10.003Associated cell lines:
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Sevilla A, Forero E, Zimmer M, Martinez H, Reggio K, Paull D, Egli D, Noggle S
Derivation and characterization of the NYSCFe003-A human embryonic stem cell line
Sevilla A et al. Derivation and characterization of the NYSCFe003-A human embryonic stem cell line. . 2017-12-00. Pubmed ID: 29161648; DOI: 10.1016/j.scr.2017.10.017 NYSCFe003-A 2017-12-00 2017-12-00 PubMed: 29161648 DOI: 10.1016/j.scr.2017.10.017Associated cell lines:
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Matloka M, Klein AF, Rau F, Furling D
Cells of Matter-In Vitro Models for Myotonic Dystrophy
Matloka M et al. Cells of Matter-In Vitro Models for Myotonic Dystrophy. . 2018-00-00. Pubmed ID: 29875732; DOI: 10.3389/fneur.2018.00361; PMC: PMC5974047 CHUQi001-A 2018-00-00 2018-00-00 PubMed: 29875732 DOI: 10.3389/fneur.2018.00361Associated cell lines:
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Skrzypczyk A, Kehr S, Krystel I, Bernhart SH, Giri S, Bader A, Stadler PF
Noncoding RNA Transcripts during Differentiation of Induced Pluripotent Stem Cells into Hepatocytes
Skrzypczyk A et al. Noncoding RNA Transcripts during Differentiation of Induced Pluripotent Stem Cells into Hepatocytes. . 2018-00-00. Pubmed ID: 30210551; DOI: 10.1155/2018/5692840; PMC: PMC6120260 ULEIi001-A 2018-00-00 2018-00-00 PubMed: 30210551 DOI: 10.1155/2018/5692840Associated cell lines:
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André LM, Ausems CRM, Wansink DG, Wieringa B
Abnormalities in Skeletal Muscle Myogenesis, Growth, and Regeneration in Myotonic Dystrophy
André LM et al. Abnormalities in Skeletal Muscle Myogenesis, Growth, and Regeneration in Myotonic Dystrophy. . 2018-00-00. Pubmed ID: 29892259; DOI: 10.3389/fneur.2018.00368; PMC: PMC5985300 CHUQi001-A 2018-00-00 2018-00-00 PubMed: 29892259 DOI: 10.3389/fneur.2018.00368Associated cell lines:
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Evert BO, Nalavade R, Jungverdorben J, Matthes F, Weber S, Rajput A, Bonn S, Brüstle O, Peitz M, Krauß S
Upregulation of miR-370 and miR-543 is associated with reduced expression of heat shock protein 40 in spinocerebellar ataxia type 3
Evert BO et al. Upregulation of miR-370 and miR-543 is associated with reduced expression of heat shock protein 40 in spinocerebellar ataxia type 3. . 2018-00-00. Pubmed ID: 30086154; DOI: 10.1371/journal.pone.0201794; PMC: PMC6080806 UKBi005-A 2018-00-00 2018-00-00 PubMed: 30086154 DOI: 10.1371/journal.pone.0201794Associated cell lines:
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González-Pozas F, Montes R, Domingo-Reinés J, Ayllón V, Ramos-Mejía V
Establishment of 2 control and 2 hPSC cell lines constitutively expressing the Notch ligand DLL4
González-Pozas F et al. Establishment of 2 control and 2 hPSC cell lines constitutively expressing the Notch ligand DLL4. . 2017-12-00. Pubmed ID: 29246573; DOI: 10.1016/j.scr.2017.07.008 WAe009-AGENYOi001-AGENYOi001-A-1GENYOi001-A-2WAe009-A-5WAe009-A-6 2017-12-00 2017-12-00 PubMed: 29246573 DOI: 10.1016/j.scr.2017.07.008Associated cell lines:
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Zhang Y, Zhu J, Dai Y, Wang L, Liu R
Development of one control and one tumor-specific induced pluripotent stem cell line from laryngeal carcinoma patient
Zhang Y et al. Development of one control and one tumor-specific induced pluripotent stem cell line from laryngeal carcinoma patient. . 2017-12-00. Pubmed ID: 29246575; DOI: 10.1016/j.scr.2017.07.027 ZZUi001-AZZUi002-A 2017-12-00 2017-12-00 PubMed: 29246575 DOI: 10.1016/j.scr.2017.07.027 -
Wang Y, Sun H, Wang Z, Yang Z, Shi M, Yang J, Liu Y, Liu H, Zhang S, Shi C, Xu Y
Generation of induced pluripotent stem cell line (ZZUi005-A) from a 21-year-old patient with a novel RAB39B gene mutation in X-linked juvenile parkinsonism
Wang Y et al. Generation of induced pluripotent stem cell line (ZZUi005-A) from a 21-year-old patient with a novel RAB39B gene mutation in X-linked juvenile parkinsonism. . 2017-12-00. Pubmed ID: 29128816; DOI: 10.1016/j.scr.2017.10.021 ZZUi005-A 2017-12-00 2017-12-00 PubMed: 29128816 DOI: 10.1016/j.scr.2017.10.021Associated cell lines:
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Hsu YH, Wu YT, Huang CY, Ho MC, Cheng YC, Syu SH, Lu HE, Chen YC, Tsai CL, Lin HC, Wei YH, Hsu YC, Hsieh PCH
Generation of an induced pluripotent stem cell line from a 39-year-old female patient with severe-to-profound non-syndromic sensorineural hearing loss and a A1555G mutation in the mitochondrial MTRNR1 gene
Hsu YH et al. Generation of an induced pluripotent stem cell line from a 39-year-old female patient with severe-to-profound non-syndromic sensorineural hearing loss and a A1555G mutation in the mitochondrial MTRNR1 gene. . 2017-12-00. Pubmed ID: 29174977; DOI: 10.1016/j.scr.2017.10.024 IBMSi004-A 2017-12-00 2017-12-00 PubMed: 29174977 DOI: 10.1016/j.scr.2017.10.024Associated cell lines:
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Harmuth T, Prell-Schicker C, Weber JJ, Gellerich F, Funke C, Drießen S, Magg JCD, Krebiehl G, Wolburg H, Hayer SN, Hauser S, Krüger R, Schöls L, Riess O, Hübener-Schmid J
Mitochondrial Morphology, Function and Homeostasis Are Impaired by Expression of an N-terminal Calpain Cleavage Fragment of Ataxin-3
Harmuth T et al. Mitochondrial Morphology, Function and Homeostasis Are Impaired by Expression of an N-terminal Calpain Cleavage Fragment of Ataxin-3. . 2018-00-00. Pubmed ID: 30364204; DOI: 10.3389/fnmol.2018.00368; PMC: PMC6192284 HIHCNi002-A 2018-00-00 2018-00-00 PubMed: 30364204 DOI: 10.3389/fnmol.2018.00368Associated cell lines:
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Lee JJ, Ho MC, Huang CY, Wen CH, Cheng YC, Hsu YH, Hwang DY, Lu HE, Chen HC, Hsieh PCH
Induced pluripotent stem cells derived from an autosomal dominant polycystic kidney disease patient carrying a PKD1 Q533X mutation
Lee JJ et al. Induced pluripotent stem cells derived from an autosomal dominant polycystic kidney disease patient carrying a PKD1 Q533X mutation. . 2017-12-00. Pubmed ID: 29121521; DOI: 10.1016/j.scr.2017.10.026 IBMSi002-A 2017-12-00 2017-12-00 PubMed: 29121521 DOI: 10.1016/j.scr.2017.10.026Associated cell lines:
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Wang Y, Zhang Y, Zhang J, Lu J, Yang C, Zhao J, Li G, Liu Z, Lei Y
Generation of a human control PBMC derived iPS cell line TUSMi001-A from a healthy male donor of Han Chinese genetic background
Wang Y et al. Generation of a human control PBMC derived iPS cell line TUSMi001-A from a healthy male donor of Han Chinese genetic background. . 2017-12-00. Pubmed ID: 29035843; DOI: 10.1016/j.scr.2017.10.006 TUSMi001-A 2017-12-00 2017-12-00 PubMed: 29035843 DOI: 10.1016/j.scr.2017.10.006Associated cell lines:
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Cristo F, Inácio JM, Rosas G, Carreira IM, Melo JB, de Almeida LP, Mendes P, Martins DS, Maio J, Anjos R, Belo JA
Generation of human iPSC line from a patient with laterality defects and associated congenital heart anomalies carrying a DAND5 missense alteration
Cristo F et al. Generation of human iPSC line from a patient with laterality defects and associated congenital heart anomalies carrying a DAND5 missense alteration. . 2017-12-00. Pubmed ID: 29136563; DOI: 10.1016/j.scr.2017.10.019 NMSUNLi001-A 2017-12-00 2017-12-00 PubMed: 29136563 DOI: 10.1016/j.scr.2017.10.019Associated cell lines:
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Re S, Dogan AA, Ben-Shachar D, Berger G, Werling AM, Walitza S, Grünblatt E
Improved Generation of Induced Pluripotent Stem Cells From Hair Derived Keratinocytes - A Tool to Study Neurodevelopmental Disorders as ADHD
Re S et al. Improved Generation of Induced Pluripotent Stem Cells From Hair Derived Keratinocytes - A Tool to Study Neurodevelopmental Disorders as ADHD. . 2018-00-00. Pubmed ID: 30319360; DOI: 10.3389/fncel.2018.00321; PMC: PMC6167495 MUSIi006-A 2018-00-00 2018-00-00 PubMed: 30319360 DOI: 10.3389/fncel.2018.00321Associated cell lines:
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Steenpass L
Generation of two H1 hESC sublines carrying a heterozygous and homozygous knock-out of RB1
Steenpass L. Generation of two H1 hESC sublines carrying a heterozygous and homozygous knock-out of RB1. . 2017-12-00. Pubmed ID: 29246572; DOI: 10.1016/j.scr.2017.07.005 WAe001-AWAe001-A-10WAe001-A-11 2017-12-00 2017-12-00 PubMed: 29246572 DOI: 10.1016/j.scr.2017.07.005Associated cell lines:
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Ho MC, Huang CY, Lee JJ, Hsu SH, Cheng YC, Hsu YH, Hwang DY, Lu HE, Chen HC, Hsieh PCH
Generation of an induced pluripotent stem cell line, IBMS-iPSC-014-05, from a female autosomal dominant polycystic kidney disease patient carrying a common mutation of R803X in PKD2
Ho MC et al. Generation of an induced pluripotent stem cell line, IBMS-iPSC-014-05, from a female autosomal dominant polycystic kidney disease patient carrying a common mutation of R803X in PKD2. . 2017-12-00. Pubmed ID: 29055226; DOI: 10.1016/j.scr.2017.10.005 IBMSi003-A 2017-12-00 2017-12-00 PubMed: 29055226 DOI: 10.1016/j.scr.2017.10.005Associated cell lines:
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Zafar F, Valappil RA, Kim S, Johansen KK, Chang ALS, Tetrud JW, Eis PS, Hatchwell E, Langston JW, Dickson DW, Schüle B
Genetic fine-mapping of the Iowan SNCA gene triplication in a patient with Parkinson's disease
Zafar F et al. Genetic fine-mapping of the Iowan SNCA gene triplication in a patient with Parkinson's disease. . 2018-00-00. Pubmed ID: 29928688; DOI: 10.1038/s41531-018-0054-4; PMC: PMC6003950 SUSMi005-A 2018-00-00 2018-00-00 PubMed: 29928688 DOI: 10.1038/s41531-018-0054-4Associated cell lines:
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Steele-Stallard HB, Pinton L, Sarcar S, Ozdemir T, Maffioletti SM, Zammit PS, Tedesco FS
Modeling Skeletal Muscle Laminopathies Using Human Induced Pluripotent Stem Cells Carrying Pathogenic LMNA Mutations
Steele-Stallard HB et al. Modeling Skeletal Muscle Laminopathies Using Human Induced Pluripotent Stem Cells Carrying Pathogenic LMNA Mutations. . 2018-00-00. Pubmed ID: 30405424; DOI: 10.3389/fphys.2018.01332; PMC: PMC6201196 CMDi001-ACMDi002-ACMDi003-ACMDi004-ACMDi005-A 2018-00-00 2018-00-00 PubMed: 30405424 DOI: 10.3389/fphys.2018.01332 -
Hansen M, Varga E, Wüst T, Mellink C, van der Kevie-Kersemaekers AM, Marneth AE, von Lindern M, van der Reijden B, van den Akker E
Generation and characterization of a human iPSC line SANi005-A containing the gray platelet associated heterozygous mutation p.Q287* in GFI1B
Hansen M et al. Generation and characterization of a human iPSC line SANi005-A containing the gray platelet associated heterozygous mutation p.Q287* in GFI1B. . 2017-12-00. Pubmed ID: 29055225; DOI: 10.1016/j.scr.2017.10.008 SANi003-ASANi005-A 2017-12-00 2017-12-00 PubMed: 29055225 DOI: 10.1016/j.scr.2017.10.008 -
Hansen M, Varga E, Wüst T, Mellink C, van der Kevie-Kersemaekers AM, von Lindern M, van den Akker E
Generation and characterization of human iPSC lines SANi001-A and SANi002-A from mobilized peripheral blood derived megakaryoblasts
Hansen M et al. Generation and characterization of human iPSC lines SANi001-A and SANi002-A from mobilized peripheral blood derived megakaryoblasts. . 2017-12-00. Pubmed ID: 29055227; DOI: 10.1016/j.scr.2017.10.002 SANi001-ASANi002-ASANi003-B 2017-12-00 2017-12-00 PubMed: 29055227 DOI: 10.1016/j.scr.2017.10.002 -
Lin CH, Cheng YC, Lin HI, Ho MC, Hsu YH, Wen CH, Ko HW, Lu HE, Huang CY, Hsieh PCH
Generation of induced pluripotent stem cells from a patient with Parkinson's disease carrying LRRK2 p.I2012T mutation
Lin CH et al. Generation of induced pluripotent stem cells from a patient with Parkinson's disease carrying LRRK2 p.I2012T mutation. . 2017-12-00. Pubmed ID: 29127874; DOI: 10.1016/j.scr.2017.10.020 IBMSi006-A 2017-12-00 2017-12-00 PubMed: 29127874 DOI: 10.1016/j.scr.2017.10.020Associated cell lines:
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Merleau-Ponty N, Vertommen S, Pucéat M
"I6 passages: on the reproduction of a human embryonic stem cell line from Israel to France"
Merleau-Ponty N et al. "I6 passages: on the reproduction of a human embryonic stem cell line from Israel to France". . 2018-00-00. Pubmed ID: 30679931; DOI: 10.1080/14636778.2018.1548269; PMC: PMC6319182 TECHe003-A 2018-00-00 2018-00-00 PubMed: 30679931 DOI: 10.1080/14636778.2018.1548269Associated cell lines:
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O'Neill AC, Kyrousi C, Einsiedler M, Burtscher I, Drukker M, Markie DM, Kirk EP, Götz M, Robertson SP, Cappello S
Mob2 Insufficiency Disrupts Neuronal Migration in the Developing Cortex
O'Neill AC et al. Mob2 Insufficiency Disrupts Neuronal Migration in the Developing Cortex. . 2018-00-00. Pubmed ID: 29593499; DOI: 10.3389/fncel.2018.00057; PMC: PMC5857600 ISFi001-A 2018-00-00 2018-00-00 PubMed: 29593499 DOI: 10.3389/fncel.2018.00057Associated cell lines:
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Brookhouser N, Zhang P, Caselli R, Kim JJ, Brafman DA
Generation and characterization of human induced pluripotent stem cell (hiPSC) lines from an Alzheimer's disease (ASUi003-A) and non-demented control (ASUi004-A) patient homozygous for the Apolipoprotein e4 (APOE4) risk variant
Brookhouser N et al. Generation and characterization of human induced pluripotent stem cell (hiPSC) lines from an Alzheimer's disease (ASUi003-A) and non-demented control (ASUi004-A) patient homozygous for the Apolipoprotein e4 (APOE4) risk variant. . 2017-12-00. Pubmed ID: 29246571; DOI: 10.1016/j.scr.2017.07.003 ASUi003-AASUi004-A 2017-12-00 2017-12-00 PubMed: 29246571 DOI: 10.1016/j.scr.2017.07.003 -
Okuno H, Renault Mihara F, Ohta S, Fukuda K, Kurosawa K, Akamatsu W, Sanosaka T, Kohyama J, Hayashi K, Nakajima K, Takahashi T, Wysocka J, Kosaki K, Okano H
CHARGE syndrome modeling using patient-iPSCs reveals defective migration of neural crest cells harboring CHD7 mutations
Okuno H et al. CHARGE syndrome modeling using patient-iPSCs reveals defective migration of neural crest cells harboring CHD7 mutations. . 2017-11-28. Pubmed ID: 29179815; DOI: 10.7554/elife.21114; PMC: PMC5705211 KUIFMSi004-CWAe029-A 2017-11-28 2017-11-28 PubMed: 29179815 DOI: 10.7554/elife.21114Associated cell lines:
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Yin J, Li J, Chen H, Wang J, Yan P, Liu M, Liu W, Lu W, Xu Z, Zhang W, Wang J, Sun Z, Ruan S
Large-area highly crystalline WSe(2) atomic layers for ultrafast pulsed lasers
Yin J et al. Large-area highly crystalline WSe(2) atomic layers for ultrafast pulsed lasers. . 2017-11-27. Pubmed ID: 29221037; DOI: 10.1364/oe.25.030020 TISSUi001-A 2017-11-27 2017-11-27 PubMed: 29221037 DOI: 10.1364/oe.25.030020Associated cell lines:
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Matson JP, Dumitru R, Coryell P, Baxley RM, Chen W, Twaroski K, Webber BR, Tolar J, Bielinsky AK, Purvis JE, Cook JG
Rapid DNA replication origin licensing protects stem cell pluripotency
Matson JP et al. Rapid DNA replication origin licensing protects stem cell pluripotency. . 2017-11-17. Pubmed ID: 29148972; DOI: 10.7554/elife.30473; PMC: PMC5720591 WAe009-A 2017-11-17 2017-11-17 PubMed: 29148972 DOI: 10.7554/elife.30473Associated cell lines:
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Siller R, Sullivan GJ
Rapid Screening of the Endodermal Differentiation Potential of Human Pluripotent Stem Cells
Siller R et al. Rapid Screening of the Endodermal Differentiation Potential of Human Pluripotent Stem Cells. . 2017-11-15. Pubmed ID: 29140570; DOI: 10.1002/cpsc.36 UIOi001-A 2017-11-15 2017-11-15 PubMed: 29140570 DOI: 10.1002/cpsc.36Associated cell lines:
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Zeng S, Liu L, Sun Y, Lu G, Lin G
Role of telomeric repeat-containing RNA in telomeric chromatin remodeling during the early expansion of human embryonic stem cells
Zeng S et al. Role of telomeric repeat-containing RNA in telomeric chromatin remodeling during the early expansion of human embryonic stem cells. . 2017-11-00. Pubmed ID: 28765174; DOI: 10.1096/fj.201600939rr NERCe003-A 2017-11-00 2017-11-00 PubMed: 28765174 DOI: 10.1096/fj.201600939rrAssociated cell lines:
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Roberts B, Haupt A, Tucker A, Grancharova T, Arakaki J, Fuqua MA, Nelson A, Hookway C, Ludmann SA, Mueller IA, Yang R, Horwitz R, Rafelski SM, Gunawardane RN
Systematic gene tagging using CRISPR/Cas9 in human stem cells to illuminate cell organization
Roberts B et al. Systematic gene tagging using CRISPR/Cas9 in human stem cells to illuminate cell organization. . 2017-10-15. Pubmed ID: 28814507; DOI: 10.1091/mbc.e17-03-0209; PMC: PMC5638588 UCSFi001-AUCSFi001-A-1UCSFi001-A-2UCSFi001-A-3UCSFi001-A-5UCSFi001-A-6UCSFi001-A-7UCSFi001-A-8UCSFi001-A-9UCSFi001-A-10UCSFi001-A-11 2017-10-15 2017-10-15 PubMed: 28814507 DOI: 10.1091/mbc.e17-03-0209Associated cell lines:
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Säljö K, Barone A, Mölne J, Rydberg L, Teneberg S, Breimer ME
HLA and Histo-Blood Group Antigen Expression in Human Pluripotent Stem Cells and their Derivatives
Säljö K et al. HLA and Histo-Blood Group Antigen Expression in Human Pluripotent Stem Cells and their Derivatives. . 2017-10-12. Pubmed ID: 29026098; DOI: 10.1038/s41598-017-12231-8; PMC: PMC5638960 CEBe012-ACEBe015-AESe019-AUODi001-ACEBi001-A 2017-10-12 2017-10-12 PubMed: 29026098 DOI: 10.1038/s41598-017-12231-8 -
Lehnen D, Barral S, Cardoso T, Grealish S, Heuer A, Smiyakin A, Kirkeby A, Kollet J, Cremer H, Parmar M, Bosio A, Knöbel S
IAP-Based Cell Sorting Results in Homogeneous Transplantable Dopaminergic Precursor Cells Derived from Human Pluripotent Stem Cells
Lehnen D et al. IAP-Based Cell Sorting Results in Homogeneous Transplantable Dopaminergic Precursor Cells Derived from Human Pluripotent Stem Cells. . 2017-10-10. Pubmed ID: 28943253; DOI: 10.1016/j.stemcr.2017.08.016; PMC: PMC5639383 MILi001-A 2017-10-10 2017-10-10 PubMed: 28943253 DOI: 10.1016/j.stemcr.2017.08.016Associated cell lines:
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Cliff TS, Wu T, Boward BR, Yin A, Yin H, Glushka JN, Prestegaard JH, Dalton S
MYC Controls Human Pluripotent Stem Cell Fate Decisions through Regulation of Metabolic Flux
Cliff TS et al. MYC Controls Human Pluripotent Stem Cell Fate Decisions through Regulation of Metabolic Flux. . 2017-10-05. Pubmed ID: 28965765; DOI: 10.1016/j.stem.2017.08.018; PMC: PMC5644510 WAe007-AWAe009-A 2017-10-05 2017-10-05 PubMed: 28965765 DOI: 10.1016/j.stem.2017.08.018 -
Tian L, Eldridge L, Chaudhari P, Zhang L, Anders RA, Schwarz KB, Ye Z, Jang YY
Derivation of a disease-specific human induced pluripotent stem cell line from a biliary atresia patient
Tian L et al. Derivation of a disease-specific human induced pluripotent stem cell line from a biliary atresia patient. . 2017-10-00. Pubmed ID: 29034890; DOI: 10.1016/j.scr.2017.08.001; PMC: PMC5881114 JHUi001-A 2017-10-00 2017-10-00 PubMed: 29034890 DOI: 10.1016/j.scr.2017.08.001Associated cell lines:
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Griscelli F, Oudrhiri N, Feraud O, Divers D, Portier L, Turhan AG, Bennaceur Griscelli A
Generation of induced pluripotent stem cell (iPSC) line from a patient with triple negative breast cancer with hereditary exon 17 deletion of BRCA1 gene
Griscelli F et al. Generation of induced pluripotent stem cell (iPSC) line from a patient with triple negative breast cancer with hereditary exon 17 deletion of BRCA1 gene. . 2017-10-00. Pubmed ID: 29034880; DOI: 10.1016/j.scr.2017.09.003 UPSFRi011-A 2017-10-00 2017-10-00 PubMed: 29034880 DOI: 10.1016/j.scr.2017.09.003Associated cell lines:
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Zurita-Díaz F, Galera-Monge T, Moreno-Izquierdo A, Corton M, Ayuso C, Garesse R, Gallardo ME
Establishment of a human DOA 'plus' iPSC line, IISHDOi003-A, with the mutation in the OPA1 gene: c.1635C>A; p.Ser545Arg
Zurita-Díaz F et al. Establishment of a human DOA 'plus' iPSC line, IISHDOi003-A, with the mutation in the OPA1 gene: c.1635C>A; p.Ser545Arg. . 2017-10-00. Pubmed ID: 29034899; DOI: 10.1016/j.scr.2017.08.017 IISHDOi003-A 2017-10-00 2017-10-00 PubMed: 29034899 DOI: 10.1016/j.scr.2017.08.017Associated cell lines:
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Gomez Limia CE, Devalle S, Reis M, Sochacki J, Carneiro M, Madeiro da Costa R, D'Andrea M, Padilha T, Zalcberg IR, Solza C, Daumas A, Rehen S, Monte-Mór B, Bonamino MH
Generation and characterization of a human induced pluripotent stem (iPS) cell line derived from an acute myeloid leukemia patient evolving from primary myelofibrosis carrying the CALR 52bp deletion and the ASXL1 p.R693X mutation
Gomez Limia CE et al. Generation and characterization of a human induced pluripotent stem (iPS) cell line derived from an acute myeloid leukemia patient evolving from primary myelofibrosis carrying the CALR 52bp deletion and the ASXL1 p.R693X mutation. . 2017-10-00. Pubmed ID: 29034885; DOI: 10.1016/j.scr.2017.08.006 INCABRi001-A 2017-10-00 2017-10-00 PubMed: 29034885 DOI: 10.1016/j.scr.2017.08.006Associated cell lines:
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Uhm KO, Go GY, Kim SJ, Jo EH, Choi HY, Im YS, Ha HY, Kim JH, Koo SK
Generation of human induced pluripotent stem cell lines from human dermal fibroblasts using a modified RNA system
Uhm KO et al. Generation of human induced pluripotent stem cell lines from human dermal fibroblasts using a modified RNA system. . 2017-10-00. Pubmed ID: 29034882; DOI: 10.1016/j.scr.2017.02.009 KSCBi002-BKSCBi002-B-1 2017-10-00 2017-10-00 PubMed: 29034882 DOI: 10.1016/j.scr.2017.02.009Associated cell lines:
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Wu J, Hunt SD, Matthias N, Servián-Morilla E, Lo J, Jafar-Nejad H, Paradas C, Darabi R
Generation of an induced pluripotent stem cell line (CSCRMi001-A) from a patient with a new type of limb-girdle muscular dystrophy (LGMD) due to a missense mutation in POGLUT1 (Rumi)
Wu J et al. Generation of an induced pluripotent stem cell line (CSCRMi001-A) from a patient with a new type of limb-girdle muscular dystrophy (LGMD) due to a missense mutation in POGLUT1 (Rumi). . 2017-10-00. Pubmed ID: 29034878; DOI: 10.1016/j.scr.2017.08.020; PMC: PMC5679726 CSCRMi001-A 2017-10-00 2017-10-00 PubMed: 29034878 DOI: 10.1016/j.scr.2017.08.020Associated cell lines:
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Xue Y, Zhu M, Qin D, Li Y, Cen X, Sun X, Lian W, Liao B
Establishment of a congenital tooth agenesis related gene MSX1 knockout human embryonic stem cell lines by CRISPR-Cas9 technology
Xue Y et al. Establishment of a congenital tooth agenesis related gene MSX1 knockout human embryonic stem cell lines by CRISPR-Cas9 technology. . 2017-10-00. Pubmed ID: 29034883; DOI: 10.1016/j.scr.2017.05.008 WAe001-A-3 2017-10-00 2017-10-00 PubMed: 29034883 DOI: 10.1016/j.scr.2017.05.008Associated cell lines:
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Khudiakov A, Kostina D, Zlotina A, Yany N, Sergushichev A, Pervunina T, Tomilin A, Kostareva A, Malashicheva A
Generation of iPSC line from patient with arrhythmogenic right ventricular cardiomyopathy carrying mutations in PKP2 gene
Khudiakov A et al. Generation of iPSC line from patient with arrhythmogenic right ventricular cardiomyopathy carrying mutations in PKP2 gene. . 2017-10-00. Pubmed ID: 29034900; DOI: 10.1016/j.scr.2017.08.014 FAMRCi001-A 2017-10-00 2017-10-00 PubMed: 29034900 DOI: 10.1016/j.scr.2017.08.014Associated cell lines:
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Wang Y, Zhang J, Zhang Y, Huang D, Zhao J, Li G, Lei Y
Generation of a human induced pluripotent stem cell line from a 65-year old healthy female donor with Chinese Han genetic background
Wang Y et al. Generation of a human induced pluripotent stem cell line from a 65-year old healthy female donor with Chinese Han genetic background. . 2017-10-00. Pubmed ID: 29034892; DOI: 10.1016/j.scr.2017.08.008 TUSMi002-A 2017-10-00 2017-10-00 PubMed: 29034892 DOI: 10.1016/j.scr.2017.08.008Associated cell lines:
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Miquel-Serra L, Duarri A, Muñoz Y, Kuebler B, Aran B, Costa C, Martí M, Comabella M, Malhotra S, Montalban X, Veiga A, Raya A
Generation of six multiple sclerosis patient-derived induced pluripotent stem cell lines
Miquel-Serra L et al. Generation of six multiple sclerosis patient-derived induced pluripotent stem cell lines. . 2017-10-00. Pubmed ID: 29034884; DOI: 10.1016/j.scr.2017.06.001 ESi048-AESi049-AESi050-AESi051-AESi052-AESi053-A 2017-10-00 2017-10-00 PubMed: 29034884 DOI: 10.1016/j.scr.2017.06.001 -
Khudiakov A, Kostina D, Zlotina A, Nikulina T, Sergushichev A, Gudkova A, Tomilin A, Malashicheva A, Kostareva A
Generation of iPSC line from desmin-related cardiomyopathy patient carrying splice site mutation of DES gene
Khudiakov A et al. Generation of iPSC line from desmin-related cardiomyopathy patient carrying splice site mutation of DES gene. . 2017-10-00. Pubmed ID: 29034897; DOI: 10.1016/j.scr.2017.08.015 FAMRCi002-A 2017-10-00 2017-10-00 PubMed: 29034897 DOI: 10.1016/j.scr.2017.08.015Associated cell lines:
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Brookhouser N, Zhang P, Caselli R, Kim JJ, Brafman DA
Generation and characterization of human induced pluripotent stem cell (hiPSC) lines from an Alzheimer's disease (ASUi001-A) and non-demented control (ASUi002-A) patient homozygous for the Apolipoprotein e4 (APOE4) risk variant
Brookhouser N et al. Generation and characterization of human induced pluripotent stem cell (hiPSC) lines from an Alzheimer's disease (ASUi001-A) and non-demented control (ASUi002-A) patient homozygous for the Apolipoprotein e4 (APOE4) risk variant. . 2017-10-00. Pubmed ID: 29034886; DOI: 10.1016/j.scr.2017.06.003 ASUi001-AASUi002-A 2017-10-00 2017-10-00 PubMed: 29034886 DOI: 10.1016/j.scr.2017.06.003 -
Xu M, Stattin EL, Murphy M, Barry F
Generation of induced pluripotent stem cells (ARO-iPSC1-11) from a patient with autosomal recessive osteopetrosis harboring the c.212+1G>T mutation in SNX10 gene
Xu M et al. Generation of induced pluripotent stem cells (ARO-iPSC1-11) from a patient with autosomal recessive osteopetrosis harboring the c.212+1G>T mutation in SNX10 gene. . 2017-10-00. Pubmed ID: 29034896; DOI: 10.1016/j.scr.2017.07.024 NUIGi001-A 2017-10-00 2017-10-00 PubMed: 29034896 DOI: 10.1016/j.scr.2017.07.024Associated cell lines:
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Terray A, Slembrouck A, Nanteau C, Chondroyer C, Zeitz C, Sahel JA, Audo I, Reichman S, Goureau O
Generation of an induced pluripotent stem cell (iPSC) line from a patient with autosomal dominant retinitis pigmentosa due to a mutation in the NR2E3 gene
Terray A et al. Generation of an induced pluripotent stem cell (iPSC) line from a patient with autosomal dominant retinitis pigmentosa due to a mutation in the NR2E3 gene. . 2017-10-00. Pubmed ID: 29034877; DOI: 10.1016/j.scr.2017.08.003 IDVi001-A 2017-10-00 2017-10-00 PubMed: 29034877 DOI: 10.1016/j.scr.2017.08.003Associated cell lines:
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Murakami N, Ishikawa T, Kondo T, Imamura K, Tsukita K, Enami T, Funayama M, Shibukawa R, Matsumoto S, Izumi Y, Ohta E, Obata F, Kaji R, Inoue H
Establishment of DYT5 patient-specific induced pluripotent stem cells with a GCH1 mutation
Murakami N et al. Establishment of DYT5 patient-specific induced pluripotent stem cells with a GCH1 mutation. . 2017-10-00. Pubmed ID: 29034893; DOI: 10.1016/j.scr.2017.07.029 CIRAi001-A 2017-10-00 2017-10-00 PubMed: 29034893 DOI: 10.1016/j.scr.2017.07.029Associated cell lines:
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Huang CY, Ho MC, Lee JJ, Hwang DY, Ko HW, Cheng YC, Hsu YH, Lu HE, Chen HC, Hsieh PCH
Generation of induced pluripotent stem cells derived from an autosomal dominant polycystic kidney disease patient with a p.Ser1457fs mutation in PKD1
Huang CY et al. Generation of induced pluripotent stem cells derived from an autosomal dominant polycystic kidney disease patient with a p.Ser1457fs mutation in PKD1. . 2017-10-00. Pubmed ID: 29034881; DOI: 10.1016/j.scr.2017.09.004 IBMSi001-A 2017-10-00 2017-10-00 PubMed: 29034881 DOI: 10.1016/j.scr.2017.09.004Associated cell lines:
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Sekine SI, Kondo T, Murakami N, Imamura K, Enami T, Shibukawa R, Tsukita K, Funayama M, Inden M, Kurita H, Hozumi I, Inoue H
Induced pluripotent stem cells derived from a patient with familial idiopathic basal ganglia calcification (IBGC) caused by a mutation in SLC20A2 gene
Sekine SI et al. Induced pluripotent stem cells derived from a patient with familial idiopathic basal ganglia calcification (IBGC) caused by a mutation in SLC20A2 gene. . 2017-10-00. Pubmed ID: 29034894; DOI: 10.1016/j.scr.2017.07.028 CIRAi003-A 2017-10-00 2017-10-00 PubMed: 29034894 DOI: 10.1016/j.scr.2017.07.028Associated cell lines:
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Son D, Kang PJ, Yun W, You S
Generation of induced pluripotent stem cell (iPSC) line from Charcot-Marie-Tooth disease patient with MPZ mutation (CMT1B)
Son D et al. Generation of induced pluripotent stem cell (iPSC) line from Charcot-Marie-Tooth disease patient with MPZ mutation (CMT1B). . 2017-10-00. Pubmed ID: 29034895; DOI: 10.1016/j.scr.2017.08.002 KUCFRi002-A 2017-10-00 2017-10-00 PubMed: 29034895 DOI: 10.1016/j.scr.2017.08.002Associated cell lines:
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Mora C, Serzanti M, Giacomelli A, Turco V, Marchina E, Bertini V, Piovani G, Savio G, Refsgaard L, Olesen MS, Cortellini V, Dell'Era P
Generation of induced pluripotent stem cells (iPSC) from an atrial fibrillation patient carrying a KCNA5 p.D322H mutation
Mora C et al. Generation of induced pluripotent stem cells (iPSC) from an atrial fibrillation patient carrying a KCNA5 p.D322H mutation. . 2017-10-00. Pubmed ID: 29034891; DOI: 10.1016/j.scr.2017.08.009 UNIBSi001-A 2017-10-00 2017-10-00 PubMed: 29034891 DOI: 10.1016/j.scr.2017.08.009Associated cell lines:
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Mora C, Serzanti M, Giacomelli A, Beltramone S, Marchina E, Bertini V, Piovani G, Refsgaard L, Olesen MS, Cortellini V, Dell'Era P
Generation of induced pluripotent stem cells (iPSC) from an atrial fibrillation patient carrying a PITX2 p.M200V mutation
Mora C et al. Generation of induced pluripotent stem cells (iPSC) from an atrial fibrillation patient carrying a PITX2 p.M200V mutation. . 2017-10-00. Pubmed ID: 29034898; DOI: 10.1016/j.scr.2017.08.007 UNIBSi003-A 2017-10-00 2017-10-00 PubMed: 29034898 DOI: 10.1016/j.scr.2017.08.007Associated cell lines:
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Yuan F, Guo D, Gao G, Liu Y, Xu Y, Wu Y, Yang F, Ke X, Lai K, Hong L, Li YX
Generation of a KCNJ11 homozygous knockout human embryonic stem cell line WAe001-A-12 using CRISPR/Cas9
Yuan F et al. Generation of a KCNJ11 homozygous knockout human embryonic stem cell line WAe001-A-12 using CRISPR/Cas9. . 2017-10-00. Pubmed ID: 29034901; DOI: 10.1016/j.scr.2017.08.016 WAe001-AWAe001-A-12 2017-10-00 2017-10-00 PubMed: 29034901 DOI: 10.1016/j.scr.2017.08.016Associated cell lines:
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Liu Y, Ruzi A, Guo D, Wu F, Liu H, Wu H, Wu Y, Yuan F, Zhuang Y, Yang F, Lai K, Lai L, Li YX
Generation of two MEN1 knockout lines from a human embryonic stem cell line
Liu Y et al. Generation of two MEN1 knockout lines from a human embryonic stem cell line. . 2017-10-00. Pubmed ID: 29034888; DOI: 10.1016/j.scr.2017.06.005 WAe001-AWAe001-A-4WAe001-A-5 2017-10-00 2017-10-00 PubMed: 29034888 DOI: 10.1016/j.scr.2017.06.005Associated cell lines:
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Liu Y, Wu F, Zhuang Y, Guo D, Abbas N, Wei R, Wang K, Chen Y, Tao J, Wu Y, Yuan F, Pan T, Yang F, Lai K, Lai L, Li YX
Generation of three miR-122 knockout lines from a human embryonic stem cell line
Liu Y et al. Generation of three miR-122 knockout lines from a human embryonic stem cell line. . 2017-10-00. Pubmed ID: 29034887; DOI: 10.1016/j.scr.2017.06.004 WAe001-AWAe001-A-7WAe001-A-8WAe001-A-9 2017-10-00 2017-10-00 PubMed: 29034887 DOI: 10.1016/j.scr.2017.06.004Associated cell lines:
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Tan GW, Kondo T, Murakami N, Imamura K, Enami T, Tsukita K, Shibukawa R, Funayama M, Matsumoto R, Ikeda A, Takahashi R, Inoue H
Induced pluripotent stem cells derived from an autosomal dominant lateral temporal epilepsy (ADLTE) patient carrying S473L mutation in leucine-rich glioma inactivated 1 (LGI1)
Tan GW et al. Induced pluripotent stem cells derived from an autosomal dominant lateral temporal epilepsy (ADLTE) patient carrying S473L mutation in leucine-rich glioma inactivated 1 (LGI1). . 2017-10-00. Pubmed ID: 29034879; DOI: 10.1016/j.scr.2017.07.030 CIRAi002-A 2017-10-00 2017-10-00 PubMed: 29034879 DOI: 10.1016/j.scr.2017.07.030Associated cell lines:
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Liu R, Lee J, Kim BS, Wang Q, Buxton SK, Balasubramanyam N, Kim JJ, Dong J, Zhang A, Li S, Gupte AA, Hamilton DJ, Martin JF, Rodney GG, Coarfa C, Wehrens XH, Yechoor VK, Moulik M
Tead1 is required for maintaining adult cardiomyocyte function, and its loss results in lethal dilated cardiomyopathy
Liu R et al. Tead1 is required for maintaining adult cardiomyocyte function, and its loss results in lethal dilated cardiomyopathy. . 2017-09-07. Pubmed ID: 28878117; DOI: 10.1172/jci.insight.93343; PMC: PMC5621883 BCMi001-A 2017-09-07 2017-09-07 PubMed: 28878117 DOI: 10.1172/jci.insight.93343Associated cell lines:
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Mittal S, Bjørnevik K, Im DS, Flierl A, Dong X, Locascio JJ, Abo KM, Long E, Jin M, Xu B, Xiang YK, Rochet JC, Engeland A, Rizzu P, Heutink P, Bartels T, Selkoe DJ, Caldarone BJ, Glicksman MA, Khurana V, Schüle B, Park DS, Riise T, Scherzer CR
β2-Adrenoreceptor is a regulator of the α-synuclein gene driving risk of Parkinson's disease
Mittal S et al. β2-Adrenoreceptor is a regulator of the α-synuclein gene driving risk of Parkinson's disease. . 2017-09-01. Pubmed ID: 28860381; DOI: 10.1126/science.aaf3934; PMC: PMC5761666 SUSMi005-A 2017-09-01 2017-09-01 PubMed: 28860381 DOI: 10.1126/science.aaf3934Associated cell lines:
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Kikuchi T, Morizane A, Doi D, Okita K, Nakagawa M, Yamakado H, Inoue H, Takahashi R, Takahashi J
Idiopathic Parkinson's disease patient-derived induced pluripotent stem cells function as midbrain dopaminergic neurons in rodent brains
Kikuchi T et al. Idiopathic Parkinson's disease patient-derived induced pluripotent stem cells function as midbrain dopaminergic neurons in rodent brains. . 2017-09-00. Pubmed ID: 28233934; DOI: 10.1002/jnr.24014 KUIMSi012-A 2017-09-00 2017-09-00 PubMed: 28233934 DOI: 10.1002/jnr.24014Associated cell lines:
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Kikuchi T, Morizane A, Doi D, Magotani H, Onoe H, Hayashi T, Mizuma H, Takara S, Takahashi R, Inoue H, Morita S, Yamamoto M, Okita K, Nakagawa M, Parmar M, Takahashi J
Human iPS cell-derived dopaminergic neurons function in a primate Parkinson's disease model
Kikuchi T et al. Human iPS cell-derived dopaminergic neurons function in a primate Parkinson's disease model. . 2017-08-30. Pubmed ID: 28858313; DOI: 10.1038/nature23664 KUIMSi012-A 2017-08-30 2017-08-30 PubMed: 28858313 DOI: 10.1038/nature23664Associated cell lines:
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Haenseler W, Zambon F, Lee H, Vowles J, Rinaldi F, Duggal G, Houlden H, Gwinn K, Wray S, Luk KC, Wade-Martins R, James WS, Cowley SA
Excess α-synuclein compromises phagocytosis in iPSC-derived macrophages
Haenseler W et al. Excess α-synuclein compromises phagocytosis in iPSC-derived macrophages. . 2017-08-21. Pubmed ID: 28827786; DOI: 10.1038/s41598-017-09362-3; PMC: PMC5567139 STBCi019-ASTBCi023-BSTBCi023-CSTBCi024-ASTBCi024-BSTBCi024-CSTBCi026-ASTBCi019-CSTBCi026-CSTBCi026-DSTBCi044-ASTBCi063-ASTBCi064-ASTBCi066-ASTBCi083-ASTBCi083-B 2017-08-21 2017-08-21 PubMed: 28827786 DOI: 10.1038/s41598-017-09362-3 -
Koseki H, Donegá M, Lam BY, Petrova V, van Erp S, Yeo GS, Kwok JC, Ffrench-Constant C, Eva R, Fawcett JW
Selective rab11 transport and the intrinsic regenerative ability of CNS axons
Koseki H et al. Selective rab11 transport and the intrinsic regenerative ability of CNS axons. . 2017-08-08. Pubmed ID: 28829741; DOI: 10.7554/elife.26956; PMC: PMC5779230 RCe015-ARCe021-A 2017-08-08 2017-08-08 PubMed: 28829741 DOI: 10.7554/elife.26956 -
Merkert S, Bednarski C, Göhring G, Cathomen T, Martin U
Generation of a gene-corrected isogenic control iPSC line from cystic fibrosis patient-specific iPSCs homozygous for p.Phe508del mutation mediated by TALENs and ssODN
Merkert S et al. Generation of a gene-corrected isogenic control iPSC line from cystic fibrosis patient-specific iPSCs homozygous for p.Phe508del mutation mediated by TALENs and ssODN. . 2017-08-00. Pubmed ID: 28925369; DOI: 10.1016/j.scr.2017.07.010 MHHi002-AMHHi002-A-1 2017-08-00 2017-08-00 PubMed: 28925369 DOI: 10.1016/j.scr.2017.07.010Associated cell lines:
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Gündner AL, Meyer CA, Aigner S, Christensen K, Patsch C, Jagasia R, Baumann K, Burcin M
Generation of a homozygous GBA deletion human embryonic stem cell line
Gündner AL et al. Generation of a homozygous GBA deletion human embryonic stem cell line. . 2017-08-00. Pubmed ID: 28925361; DOI: 10.1016/j.scr.2017.07.009 CEBe033-A-1 2017-08-00 2017-08-00 PubMed: 28925361 DOI: 10.1016/j.scr.2017.07.009Associated cell lines:
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Balboa D, Weltner J, Novik Y, Eurola S, Wartiovaara K, Otonkoski T
Generation of an OCT4 reporter human induced pluripotent stem cell line using CRISPR/SpCas9
Balboa D et al. Generation of an OCT4 reporter human induced pluripotent stem cell line using CRISPR/SpCas9. . 2017-08-00. Pubmed ID: 28925359; DOI: 10.1016/j.scr.2017.07.006 UHi006-A-2 2017-08-00 2017-08-00 PubMed: 28925359 DOI: 10.1016/j.scr.2017.07.006Associated cell lines:
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Shekari F, Nezari H, Chen YJ, Baharvand H, Hosseini Salekdeh G
Data for whole and mitochondrial proteome of human embryonic stem cells
Shekari F et al. Data for whole and mitochondrial proteome of human embryonic stem cells. . 2017-08-00. Pubmed ID: 28664172; DOI: 10.1016/j.dib.2017.05.036; PMC: PMC5480819 WAe009-A 2017-08-00 2017-08-00 PubMed: 28664172 DOI: 10.1016/j.dib.2017.05.036Associated cell lines:
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Klein S, Dvornik JL, Yarrabothula AR, Schaniel C
A Marfan syndrome human induced pluripotent stem cell line with a heterozygous FBN1 c.4082G>A mutation, ISMMSi002-B, for disease modeling
Klein S et al. A Marfan syndrome human induced pluripotent stem cell line with a heterozygous FBN1 c.4082G>A mutation, ISMMSi002-B, for disease modeling. . 2017-08-00. Pubmed ID: 28925368; DOI: 10.1016/j.scr.2017.06.016 ISMMSi002-B 2017-08-00 2017-08-00 PubMed: 28925368 DOI: 10.1016/j.scr.2017.06.016Associated cell lines:
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Alonso-Barroso E, Brasil S, Briso-Montiano Á, Navarrete R, Pérez-Cerdá C, Ugarte M, Pérez B, Desviat LR, Richard E
Generation and characterization of a human iPSC line from a patient with propionic acidemia due to defects in the PCCA gene
Alonso-Barroso E et al. Generation and characterization of a human iPSC line from a patient with propionic acidemia due to defects in the PCCA gene. . 2017-08-00. Pubmed ID: 28925364; DOI: 10.1016/j.scr.2017.07.021 UAMi001-A 2017-08-00 2017-08-00 PubMed: 28925364 DOI: 10.1016/j.scr.2017.07.021Associated cell lines:
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Chen Y, Ou Z, Song B, Xian Y, Ouyang S, Xie Y, Xue Y, Sun X
Generation of integration-free induced pluripotent stem cells (GZHMUi001-A) by reprogramming peripheral blood mononuclear cells from a 47, XXX syndrome patient
Chen Y et al. Generation of integration-free induced pluripotent stem cells (GZHMUi001-A) by reprogramming peripheral blood mononuclear cells from a 47, XXX syndrome patient. . 2017-08-00. Pubmed ID: 28925367; DOI: 10.1016/j.scr.2017.06.002 GZHMUi001-A 2017-08-00 2017-08-00 PubMed: 28925367 DOI: 10.1016/j.scr.2017.06.002Associated cell lines:
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Noack C, Haupt LP, Zimmermann WH, Streckfuss-Bömeke K, Zelarayán LC
Generation of a KLF15 homozygous knockout human embryonic stem cell line using paired CRISPR/Cas9n, and human cardiomyocytes derivation
Noack C et al. Generation of a KLF15 homozygous knockout human embryonic stem cell line using paired CRISPR/Cas9n, and human cardiomyocytes derivation. . 2017-08-00. Pubmed ID: 28925362; DOI: 10.1016/j.scr.2017.07.007 ESIBIe002-AESIBIe002-A-1 2017-08-00 2017-08-00 PubMed: 28925362 DOI: 10.1016/j.scr.2017.07.007Associated cell lines:
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Griscelli F, Feraud O, Ernault T, Oudrihri N, Turhan AG, Bonnefond A, Froguel P, Bennaceur-Griscelli A
Generation of an induced pluripotent stem cell (iPSC) line from a patient with maturity-onset diabetes of the young type 13 (MODY13) with a the potassium inwardly-rectifying channel, subfamily J, member 11 (KCNJ11) mutation
Griscelli F et al. Generation of an induced pluripotent stem cell (iPSC) line from a patient with maturity-onset diabetes of the young type 13 (MODY13) with a the potassium inwardly-rectifying channel, subfamily J, member 11 (KCNJ11) mutation. . 2017-08-00. Pubmed ID: 28925365; DOI: 10.1016/j.scr.2017.07.023 UPSFRi012-A 2017-08-00 2017-08-00 PubMed: 28925365 DOI: 10.1016/j.scr.2017.07.023Associated cell lines:
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Bennaceur-Griscelli A, Hadoux J, Féraud O, Opolon P, Divers D, Gobbo E, Schlumberger M, Griscelli F, Turhan AG
Generation of an induced pluripotent stem cell line from a patient with hereditary multiple endocrine neoplasia 2B (MEN2B) syndrome with "highest risk" RET mutation
Bennaceur-Griscelli A et al. Generation of an induced pluripotent stem cell line from a patient with hereditary multiple endocrine neoplasia 2B (MEN2B) syndrome with "highest risk" RET mutation. . 2017-08-00. Pubmed ID: 28925363; DOI: 10.1016/j.scr.2017.07.022 UPSFRi010-A 2017-08-00 2017-08-00 PubMed: 28925363 DOI: 10.1016/j.scr.2017.07.022Associated cell lines:
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Ortuño-Costela MDC, Rodríguez-Mancera N, García-López M, Zurita-Díaz F, Moreno-Izquierdo A, Lucía A, Martín MÁ, Garesse R, Gallardo ME
Establishment of a human iPSC line (IISHDOi001-A) from a patient with McArdle disease
Ortuño-Costela MDC et al. Establishment of a human iPSC line (IISHDOi001-A) from a patient with McArdle disease. . 2017-08-00. Pubmed ID: 28925366; DOI: 10.1016/j.scr.2017.07.020 IISHDOi001-A 2017-08-00 2017-08-00 PubMed: 28925366 DOI: 10.1016/j.scr.2017.07.020Associated cell lines:
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Zheng X, Zhu Z, Chen K, Guo S, Liu T, Liu H
Establishment of an induced pluripotent stem cell line ZZUi003-A from a 65-year-old male with sporadic Parkinson's disease
Zheng X et al. Establishment of an induced pluripotent stem cell line ZZUi003-A from a 65-year-old male with sporadic Parkinson's disease. . 2017-08-00. Pubmed ID: 28925360; DOI: 10.1016/j.scr.2017.07.004 ZZUi003-A 2017-08-00 2017-08-00 PubMed: 28925360 DOI: 10.1016/j.scr.2017.07.004Associated cell lines:
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Gu Q, Wang J, Wang L, Liu ZX, Zhu WW, Tan YQ, Han WF, Wu J, Feng CJ, Fang JH, Liu L, Wang L, Li W, Zhao XY, Hu BY, Hao J, Zhou Q
Accreditation of Biosafe Clinical-Grade Human Embryonic Stem Cells According to Chinese Regulations
Gu Q et al. Accreditation of Biosafe Clinical-Grade Human Embryonic Stem Cells According to Chinese Regulations. . 2017-07-11. Pubmed ID: 28506532; DOI: 10.1016/j.stemcr.2017.04.017; PMC: PMC5511037 IOZe001-AIOZe002-A 2017-07-11 2017-07-11 PubMed: 28506532 DOI: 10.1016/j.stemcr.2017.04.017 -
Múnera JO, Sundaram N, Rankin SA, Hill D, Watson C, Mahe M, Vallance JE, Shroyer NF, Sinagoga KL, Zarzoso-Lacoste A, Hudson JR, Howell JC, Chatuvedi P, Spence JR, Shannon JM, Zorn AM, Helmrath MA, Wells JM
Differentiation of Human Pluripotent Stem Cells into Colonic Organoids via Transient Activation of BMP Signaling
Múnera JO et al. Differentiation of Human Pluripotent Stem Cells into Colonic Organoids via Transient Activation of BMP Signaling. . 2017-07-06. Pubmed ID: 28648364; DOI: 10.1016/j.stem.2017.05.020; PMC: PMC5531599 CCHMCi001-ACUSTOMi001-A 2017-07-06 2017-07-06 PubMed: 28648364 DOI: 10.1016/j.stem.2017.05.020Associated cell lines:
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Susaimanickam PJ, Maddileti S, Pulimamidi VK, Boyinpally SR, Naik RR, Naik MN, Reddy GB, Sangwan VS, Mariappan I
Generating minicorneal organoids from human induced pluripotent stem cells
Susaimanickam PJ et al. Generating minicorneal organoids from human induced pluripotent stem cells. . 2017-07-01. Pubmed ID: 28559289; DOI: 10.1242/dev.143040 LVPEIi001-A 2017-07-01 2017-07-01 PubMed: 28559289 DOI: 10.1242/dev.143040Associated cell lines:
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Balboa D, Weltner J, Novik Y, Eurola S, Wartiovaara K, Otonkoski T
Generation of a SOX2 reporter human induced pluripotent stem cell line using CRISPR/SaCas9
Balboa D et al. Generation of a SOX2 reporter human induced pluripotent stem cell line using CRISPR/SaCas9. . 2017-07-00. Pubmed ID: 28952927; DOI: 10.1016/j.scr.2017.05.005 UHi006-A-1 2017-07-00 2017-07-00 PubMed: 28952927 DOI: 10.1016/j.scr.2017.05.005Associated cell lines:
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Xu Y, Wu Y, Guo D, Gao G, Lai K, Yang F, Wang K, Wu H, Lai L, Li J, Xu K, Li YX
Generation of an ASGR1 homozygous mutant human embryonic stem cell line WAe001-A-6 using CRISPR/Cas9
Xu Y et al. Generation of an ASGR1 homozygous mutant human embryonic stem cell line WAe001-A-6 using CRISPR/Cas9. . 2017-07-00. Pubmed ID: 28952928; DOI: 10.1016/j.scr.2017.05.006 WAe001-AWAe001-A-6 2017-07-00 2017-07-00 PubMed: 28952928 DOI: 10.1016/j.scr.2017.05.006Associated cell lines:
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Kuusela J, Larsson K, Shah D, Prajapati C, Aalto-Setälä K
Low extracellular potassium prolongs repolarization and evokes early afterdepolarization in human induced pluripotent stem cell-derived cardiomyocytes
Kuusela J et al. Low extracellular potassium prolongs repolarization and evokes early afterdepolarization in human induced pluripotent stem cell-derived cardiomyocytes. . 2017-06-15. Pubmed ID: 28619993; DOI: 10.1242/bio.024216; PMC: PMC5483019 TAUi006-BTAUi007-A 2017-06-15 2017-06-15 PubMed: 28619993 DOI: 10.1242/bio.024216 -
Kilpinen H, Goncalves A, Leha A, Afzal V, Alasoo K, Ashford S, Bala S, Bensaddek D, Casale FP, Culley OJ, Danecek P, Faulconbridge A, Harrison PW, Kathuria A, McCarthy D, McCarthy SA, Meleckyte R, Memari Y, Moens N, Soares F, Mann A, Streeter I, Agu CA, Alderton A, Nelson R, Harper S, Patel M, White A, Patel SR, Clarke L, Halai R, Kirton CM, Kolb-Kokocinski A, Beales P, Birney E, Danovi D, Lamond AI, Ouwehand WH, Vallier L, Watt FM, Durbin R, Stegle O, Gaffney DJ
Common genetic variation drives molecular heterogeneity in human iPSCs
Kilpinen H et al. Common genetic variation drives molecular heterogeneity in human iPSCs. . 2017-06-15. Pubmed ID: 28489815; DOI: 10.1038/nature22403; PMC: PMC5524171 WTSIi001-AWTSIi002-AWTSIi003-AWTSIi004-AWTSIi005-AWTSIi006-AWTSIi007-AWTSIi008-AWTSIi009-AWTSIi010-AWTSIi011-AWTSIi012-AWTSIi013-AWTSIi014-AWTSIi015-AWTSIi016-AWTSIi017-AWTSIi018-AWTSIi019-AWTSIi020-AWTSIi021-AWTSIi022-AWTSIi023-AWTSIi024-AWTSIi025-AWTSIi026-AWTSIi027-AWTSIi028-AWTSIi029-AWTSIi030-AWTSIi031-AWTSIi032-AWTSIi037-AWTSIi038-AWTSIi039-AWTSIi040-AWTSIi041-AWTSIi042-AWTSIi018-BWTSIi015-BWTSIi014-BWTSIi010-BWTSIi025-BWTSIi021-BWTSIi044-AWTSIi045-AWTSIi005-BWTSIi004-BWTSIi046-AWTSIi022-BWTSIi047-AWTSIi038-BWTSIi048-AWTSIi047-BWTSIi006-BWTSIi049-AWTSIi019-BWTSIi030-BWTSIi049-BWTSIi050-AWTSIi051-AWTSIi052-AWTSIi053-AWTSIi054-AWTSIi055-AWTSIi056-AWTSIi057-AWTSIi058-AWTSIi059-AWTSIi060-AWTSIi061-AWTSIi062-AWTSIi063-AWTSIi064-AWTSIi065-AWTSIi066-AWTSIi067-AWTSIi067-BWTSIi068-AWTSIi069-AWTSIi070-AWTSIi071-AWTSIi072-AWTSIi073-AWTSIi065-BWTSIi066-BWTSIi070-BWTSIi012-BWTSIi042-BWTSIi074-AWTSIi017-BWTSIi075-AWTSIi076-AWTSIi077-AWTSIi078-AWTSIi011-BWTSIi071-BWTSIi079-AWTSIi080-AWTSIi081-AWTSIi082-AWTSIi083-AWTSIi084-AWTSIi085-AWTSIi086-AWTSIi087-AWTSIi088-AWTSIi089-AWTSIi090-AWTSIi092-AWTSIi093-AWTSIi094-AWTSIi095-AWTSIi096-AWTSIi097-AWTSIi098-AWTSIi099-AWTSIi100-AWTSIi101-AWTSIi102-AWTSIi103-AWTSIi104-AWTSIi105-AWTSIi106-AWTSIi107-AWTSIi106-BWTSIi109-AWTSIi110-AWTSIi081-BWTSIi084-BWTSIi097-BWTSIi102-BWTSIi104-BWTSIi107-BWTSIi111-AWTSIi112-AWTSIi068-BWTSIi114-AWTSIi115-AWTSIi116-AWTSIi117-AWTSIi118-AWTSIi119-AWTSIi120-AWTSIi121-AWTSIi121-BWTSIi122-AWTSIi123-AWTSIi124-AWTSIi124-BWTSIi125-AWTSIi126-AWTSIi127-AWTSIi128-AWTSIi129-AWTSIi130-AWTSIi131-AWTSIi105-BWTSIi132-AWTSIi109-BWTSIi133-AWTSIi133-BWTSIi134-AWTSIi134-BWTSIi020-BWTSIi135-AWTSIi057-BWTSIi136-AWTSIi137-AWTSIi137-BWTSIi138-AWTSIi054-BWTSIi139-AWTSIi140-AWTSIi141-AWTSIi142-AWTSIi143-AWTSIi073-BWTSIi144-AWTSIi046-BWTSIi145-AWTSIi146-AWTSIi023-BWTSIi168-AWTSIi169-AWTSIi170-AWTSIi170-BWTSIi171-AWTSIi171-BWTSIi172-AWTSIi173-AWTSIi174-AWTSIi175-AWTSIi176-AWTSIi177-AWTSIi178-AWTSIi179-AWTSIi176-BWTSIi178-BWTSIi180-AWTSIi181-AWTSIi182-AWTSIi172-BWTSIi183-AWTSIi174-BWTSIi168-BWTSIi184-AWTSIi185-AWTSIi183-BWTSIi184-BWTSIi186-AWTSIi187-AWTSIi188-AWTSIi189-AWTSIi190-AWTSIi180-BWTSIi190-BWTSIi169-BWTSIi191-AWTSIi208-AWTSIi209-AWTSIi211-AWTSIi212-AWTSIi213-AWTSIi214-AWTSIi216-AWTSIi217-AWTSIi218-AWTSIi219-AWTSIi222-AWTSIi223-AWTSIi225-AWTSIi227-AWTSIi228-AWTSIi232-AWTSIi233-AWTSIi235-AWTSIi236-AWTSIi238-AWTSIi243-AWTSIi245-AWTSIi247-AWTSIi249-AWTSIi250-AWTSIi252-AWTSIi253-AWTSIi254-AWTSIi255-AWTSIi256-AWTSIi257-AWTSIi258-AWTSIi259-AWTSIi260-AWTSIi261-AWTSIi262-AWTSIi263-AWTSIi265-AWTSIi266-AWTSIi267-AWTSIi268-AWTSIi269-AWTSIi270-AWTSIi271-AWTSIi274-AWTSIi275-AWTSIi276-AWTSIi277-AWTSIi281-AWTSIi283-AWTSIi284-AWTSIi285-AWTSIi287-AWTSIi288-AWTSIi291-AWTSIi293-AWTSIi294-AWTSIi296-AWTSIi297-AWTSIi300-AWTSIi302-AWTSIi303-AWTSIi308-AWTSIi310-AWTSIi311-AWTSIi316-AWTSIi317-AWTSIi318-AWTSIi322-AWTSIi327-AWTSIi341-AWTSIi342-AWTSIi345-AWTSIi347-AWTSIi349-AWTSIi350-AWTSIi351-AWTSIi353-AWTSIi354-AWTSIi355-AWTSIi357-AWTSIi362-AWTSIi363-AWTSIi364-AWTSIi365-AWTSIi368-AWTSIi369-AWTSIi370-AWTSIi373-AWTSIi374-AWTSIi377-AWTSIi378-AWTSIi380-AWTSIi382-AWTSIi385-AWTSIi388-AWTSIi389-AWTSIi390-AWTSIi392-AWTSIi394-AWTSIi411-AWTSIi412-AWTSIi467-AWTSIi468-AWTSIi560-AWTSIi561-AWTSIi564-AWTSIi565-AWTSIi567-AWTSIi569-AWTSIi571-AWTSIi140-BWTSIi296-BWTSIi099-BWTSIi116-BWTSIi089-BWTSIi112-BWTSIi135-BWTSIi123-BWTSIi141-BWTSIi261-BWTSIi355-BWTSIi055-BWTSIi142-BWTSIi110-BWTSIi111-BWTSIi222-BWTSIi217-BWTSIi216-BWTSIi130-BWTSIi079-BWTSIi122-BWTSIi041-BWTSIi212-BWTSIi003-BWTSIi118-BWTSIi362-BWTSIi225-BWTSIi001-BWTSIi117-BWTSIi214-BWTSIi342-BWTSIi131-BWTSIi129-BWTSIi139-BWTSIi208-BWTSIi569-BWTSIi235-BWTSIi032-BWTSIi213-BWTSIi077-BWTSIi297-BWTSIi297-DWTSIi243-BWTSIi185-BWTSIi260-BWTSIi285-BWTSIi270-BWTSIi287-BWTSIi322-BWTSIi253-BWTSIi316-BWTSIi247-BWTSIi263-BWTSIi310-BWTSIi389-BWTSIi412-BWTSIi284-BWTSIi249-BWTSIi265-BWTSIi245-BWTSIi257-BWTSIi274-BWTSIi268-BWTSIi300-BWTSIi347-BWTSIi303-BWTSIi238-BWTSIi254-BWTSIi294-BWTSIi256-BWTSIi302-BWTSIi277-BWTSIi269-BWTSIi250-BWTSIi252-BWTSIi255-BWTSIi267-BWTSIi388-BWTSIi281-BWTSIi191-BWTSIi293-BWTSIi311-BWTSIi288-BWTSIi327-B 2017-06-15 2017-06-15 PubMed: 28489815 DOI: 10.1038/nature22403 -
Shekari F, Nezari H, Larijani MR, Han CL, Baharvand H, Chen YJ, Salekdeh GH
Proteome analysis of human embryonic stem cells organelles
Shekari F et al. Proteome analysis of human embryonic stem cells organelles. . 2017-06-06. Pubmed ID: 28435121; DOI: 10.1016/j.jprot.2017.04.017 WAe009-A 2017-06-06 2017-06-06 PubMed: 28435121 DOI: 10.1016/j.jprot.2017.04.017Associated cell lines:
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Haenseler W, Sansom SN, Buchrieser J, Newey SE, Moore CS, Nicholls FJ, Chintawar S, Schnell C, Antel JP, Allen ND, Cader MZ, Wade-Martins R, James WS, Cowley SA
A Highly Efficient Human Pluripotent Stem Cell Microglia Model Displays a Neuronal-Co-culture-Specific Expression Profile and Inflammatory Response
Haenseler W et al. A Highly Efficient Human Pluripotent Stem Cell Microglia Model Displays a Neuronal-Co-culture-Specific Expression Profile and Inflammatory Response. . 2017-06-06. Pubmed ID: 28591653; DOI: 10.1016/j.stemcr.2017.05.017; PMC: PMC5470330 STBCi026-ASTBCi026-BSTBCi063-ASTBCi064-ASTBCi321-ASTBCi322-ASTBCi323-AUOXFi012-A 2017-06-06 2017-06-06 PubMed: 28591653 DOI: 10.1016/j.stemcr.2017.05.017Associated cell lines:
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Ye J, Bates N, Soteriou D, Grady L, Edmond C, Ross A, Kerby A, Lewis PA, Adeniyi T, Wright R, Poulton KV, Lowe M, Kimber SJ, Brison DR
High quality clinical grade human embryonic stem cell lines derived from fresh discarded embryos
Ye J et al. High quality clinical grade human embryonic stem cell lines derived from fresh discarded embryos. . 2017-06-05. Pubmed ID: 28583200; DOI: 10.1186/s13287-017-0561-y; PMC: PMC5460457 RCe013-ARCe015-AUMANe003-ACMFTe002-AUMANe002-AUMANe004-ACMFTe003-ACMFTe004-ACMFTe005-A 2017-06-05 2017-06-05 PubMed: 28583200 DOI: 10.1186/s13287-017-0561-yAssociated cell lines:
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Yokobayashi S, Okita K, Nakagawa M, Nakamura T, Yabuta Y, Yamamoto T, Saitou M
Clonal variation of human induced pluripotent stem cells for induction into the germ cell fate
Yokobayashi S et al. Clonal variation of human induced pluripotent stem cells for induction into the germ cell fate. . 2017-06-01. Pubmed ID: 28453617; DOI: 10.1093/biolre/iox038 KUIFMSi004-CBRCi014-A 2017-06-01 2017-06-01 PubMed: 28453617 DOI: 10.1093/biolre/iox038Associated cell lines:
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Ackermann M, Kuhn A, Kunkiel J, Merkert S, Martin U, Moritz T, Lachmann N
Ex vivo Generation of Genetically Modified Macrophages from Human Induced Pluripotent Stem Cells
Ackermann M et al. Ex vivo Generation of Genetically Modified Macrophages from Human Induced Pluripotent Stem Cells. . 2017-06-00. Pubmed ID: 28626364; DOI: 10.1159/000477129; PMC: PMC5473066 MHHi015-A 2017-06-00 2017-06-00 PubMed: 28626364 DOI: 10.1159/000477129Associated cell lines:
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Breckwoldt K, Letuffe-Brenière D, Mannhardt I, Schulze T, Ulmer B, Werner T, Benzin A, Klampe B, Reinsch MC, Laufer S, Shibamiya A, Prondzynski M, Mearini G, Schade D, Fuchs S, Neuber C, Krämer E, Saleem U, Schulze ML, Rodriguez ML, Eschenhagen T, Hansen A
Differentiation of cardiomyocytes and generation of human engineered heart tissue
Breckwoldt K et al. Differentiation of cardiomyocytes and generation of human engineered heart tissue. . 2017-06-00. Pubmed ID: 28492526; DOI: 10.1038/nprot.2017.033 UKEi003-C 2017-06-00 2017-06-00 PubMed: 28492526 DOI: 10.1038/nprot.2017.033Associated cell lines:
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Hall CE, Yao Z, Choi M, Tyzack GE, Serio A, Luisier R, Harley J, Preza E, Arber C, Crisp SJ, Watson PMD, Kullmann DM, Abramov AY, Wray S, Burley R, Loh SHY, Martins LM, Stevens MM, Luscombe NM, Sibley CR, Lakatos A, Ule J, Gandhi S, Patani R
Progressive Motor Neuron Pathology and the Role of Astrocytes in a Human Stem Cell Model of VCP-Related ALS
Hall CE et al. Progressive Motor Neuron Pathology and the Role of Astrocytes in a Human Stem Cell Model of VCP-Related ALS. . 2017-05-30. Pubmed ID: 28564594; DOI: 10.1016/j.celrep.2017.05.024; PMC: PMC5464993 UCLi009-AUCLi009-BUCLi010-AUCLi010-B 2017-05-30 2017-05-30 PubMed: 28564594 DOI: 10.1016/j.celrep.2017.05.024 -
Ludtmann MHR, Arber C, Bartolome F, de Vicente M, Preza E, Carro E, Houlden H, Gandhi S, Wray S, Abramov AY
Mutations in valosin-containing protein (VCP) decrease ADP/ATP translocation across the mitochondrial membrane and impair energy metabolism in human neurons
Ludtmann MHR et al. Mutations in valosin-containing protein (VCP) decrease ADP/ATP translocation across the mitochondrial membrane and impair energy metabolism in human neurons. . 2017-05-26. Pubmed ID: 28360103; DOI: 10.1074/jbc.m116.762898; PMC: PMC5448124 UCLi009-AUCLi009-BUCLi010-AUCLi010-B 2017-05-26 2017-05-26 PubMed: 28360103 DOI: 10.1074/jbc.m116.762898 -
Merkle FT, Ghosh S, Kamitaki N, Mitchell J, Avior Y, Mello C, Kashin S, Mekhoubad S, Ilic D, Charlton M, Saphier G, Handsaker RE, Genovese G, Bar S, Benvenisty N, McCarroll SA, Eggan K
Human pluripotent stem cells recurrently acquire and expand dominant negative P53 mutations
Merkle FT et al. Human pluripotent stem cells recurrently acquire and expand dominant negative P53 mutations. . 2017-05-11. Pubmed ID: 28445466; DOI: 10.1038/nature22312; PMC: PMC5427175 KIe007-AKIe019-AKIe022-ATECHe001-ATECHe002-ASCSe001-ASCSe002-AWAe001-AWAe007-AWAe009-AWAe013-AWAe014-ABCHe002-ABCHe003-ABCHe004-ABCHe005-ABCHe006-ASCSe003-ASCSe004-AWISCe001-ARUESe001-ASSCCe003-ASSCCe004-ASSCCe005-ASSCCe007-ASSCCe008-AKIe032-AKIe033-AWAe022-AUMANe003-ACMFTe002-AVCYTe001-AUOSe007-AUOSe008-AUOSe009-AUOSe010-AUOSe012-AUOSe013-AUOSe014-AUOSe015-AUOSe016-AUOSe017-AUOSe018-AWIBRe001-AWIBRe002-AWIBRe003-ARUESe002-AWAe023-AWAe024-AWAe025-AWAe026-AWAe027-A 2017-05-11 2017-05-11 PubMed: 28445466 DOI: 10.1038/nature22312 -
Lorenz C, Lesimple P, Bukowiecki R, Zink A, Inak G, Mlody B, Singh M, Semtner M, Mah N, Auré K, Leong M, Zabiegalov O, Lyras EM, Pfiffer V, Fauler B, Eichhorst J, Wiesner B, Huebner N, Priller J, Mielke T, Meierhofer D, Izsvák Z, Meier JC, Bouillaud F, Adjaye J, Schuelke M, Wanker EE, Lombès A, Prigione A
Human iPSC-Derived Neural Progenitors Are an Effective Drug Discovery Model for Neurological mtDNA Disorders
Lorenz C et al. Human iPSC-Derived Neural Progenitors Are an Effective Drug Discovery Model for Neurological mtDNA Disorders. . 2017-05-04. Pubmed ID: 28132834; DOI: 10.1016/j.stem.2016.12.013 HHUUKDi009-AHHUi001-AHHUi002-A 2017-05-04 2017-05-04 PubMed: 28132834 DOI: 10.1016/j.stem.2016.12.013Associated cell lines:
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Buonocore F, Kühnen P, Suntharalingham JP, Del Valle I, Digweed M, Stachelscheid H, Khajavi N, Didi M, Brady AF, Blankenstein O, Procter AM, Dimitri P, Wales JKH, Ghirri P, Knöbl D, Strahm B, Erlacher M, Wlodarski MW, Chen W, Kokai GK, Anderson G, Morrogh D, Moulding DA, McKee SA, Niemeyer CM, Grüters A, Achermann JC
Somatic mutations and progressive monosomy modify SAMD9-related phenotypes in humans
Buonocore F et al. Somatic mutations and progressive monosomy modify SAMD9-related phenotypes in humans. . 2017-05-01. Pubmed ID: 28346228; DOI: 10.1172/jci91913; PMC: PMC5409795 BIHi001-ABIHi004-ACUBi001-ACUBi002-B 2017-05-01 2017-05-01 PubMed: 28346228 DOI: 10.1172/jci91913 -
Castaño J, Bueno C, Jiménez-Delgado S, Roca-Ho H, Fraga MF, Fernandez AF, Nakanishi M, Torres-Ruiz R, Rodríguez-Perales S, Menéndez P
Generation and characterization of a human iPSC cell line expressing inducible Cas9 in the "safe harbor" AAVS1 locus
Castaño J et al. Generation and characterization of a human iPSC cell line expressing inducible Cas9 in the "safe harbor" AAVS1 locus. . 2017-05-00. Pubmed ID: 28677529; DOI: 10.1016/j.scr.2017.04.011; PMC: PMC5446316 JCLRIi001-AJCLRIi001-A-1 2017-05-00 2017-05-00 PubMed: 28677529 DOI: 10.1016/j.scr.2017.04.011Associated cell lines:
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Uhm KO, Jo EH, Go GY, Kim SJ, Choi HY, Im YS, Ha HY, Jung JW, Koo SK
Generation of human induced pluripotent stem cells from urinary cells of a healthy donor using a non-integration system
Uhm KO et al. Generation of human induced pluripotent stem cells from urinary cells of a healthy donor using a non-integration system. . 2017-05-00. Pubmed ID: 28677537; DOI: 10.1016/j.scr.2017.03.019 KSCBi001-A 2017-05-00 2017-05-00 PubMed: 28677537 DOI: 10.1016/j.scr.2017.03.019Associated cell lines:
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Marczenke M, Fell J, Piccini I, Röpke A, Seebohm G, Greber B
Generation and cardiac subtype-specific differentiation of PITX2-deficient human iPS cell lines for exploring familial atrial fibrillation
Marczenke M et al. Generation and cardiac subtype-specific differentiation of PITX2-deficient human iPS cell lines for exploring familial atrial fibrillation. . 2017-05-00. Pubmed ID: 28677534; DOI: 10.1016/j.scr.2017.03.015 HVRDe006-A 2017-05-00 2017-05-00 PubMed: 28677534 DOI: 10.1016/j.scr.2017.03.015Associated cell lines:
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Son D, Kang PJ, Yun W, You S
Generation of induced pluripotent stem cell (iPSC) line from a 36-year-old Charcot-Marie-Tooth disease patient with GJB1 mutation (CMTX)
Son D et al. Generation of induced pluripotent stem cell (iPSC) line from a 36-year-old Charcot-Marie-Tooth disease patient with GJB1 mutation (CMTX). . 2017-05-00. Pubmed ID: 28677541; DOI: 10.1016/j.scr.2017.03.006 KUCFRi001-A 2017-05-00 2017-05-00 PubMed: 28677541 DOI: 10.1016/j.scr.2017.03.006Associated cell lines:
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Haase A, Göhring G, Martin U
Generation of non-transgenic iPS cells from human cord blood CD34(+) cells under animal component-free conditions
Haase A et al. Generation of non-transgenic iPS cells from human cord blood CD34(+) cells under animal component-free conditions. . 2017-05-00. Pubmed ID: 28677540; DOI: 10.1016/j.scr.2017.03.022 MHHi001-A 2017-05-00 2017-05-00 PubMed: 28677540 DOI: 10.1016/j.scr.2017.03.022Associated cell lines:
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Lukovic D, Bolinches-Amorós A, Artero-Castro A, Pascual B, Carballo M, Hernan I, Erceg S
Generation of a human iPSC line from a patient with retinitis pigmentosa caused by mutation in PRPF8 gene
Lukovic D et al. Generation of a human iPSC line from a patient with retinitis pigmentosa caused by mutation in PRPF8 gene. . 2017-05-00. Pubmed ID: 28677533; DOI: 10.1016/j.scr.2017.03.007 RCPFi001-A 2017-05-00 2017-05-00 PubMed: 28677533 DOI: 10.1016/j.scr.2017.03.007Associated cell lines:
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Uhm KO, Kim SJ, Jo EH, Go GY, Choi HY, Im YS, Ha HY, Kim JH, Koo SK
Generation of human induced pluripotent stem cell lines from human dermal fibroblasts using a non-integration system
Uhm KO et al. Generation of human induced pluripotent stem cell lines from human dermal fibroblasts using a non-integration system. . 2017-05-00. Pubmed ID: 28677527; DOI: 10.1016/j.scr.2017.03.009 KSCBi002-A 2017-05-00 2017-05-00 PubMed: 28677527 DOI: 10.1016/j.scr.2017.03.009Associated cell lines:
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Rossbach B, Hildebrand L, El-Ahmad L, Stachelscheid H, Reinke P, Kurtz A
Generation of a human induced pluripotent stem cell line from urinary cells of a healthy donor using integration free Sendai virus technology
Rossbach B et al. Generation of a human induced pluripotent stem cell line from urinary cells of a healthy donor using integration free Sendai virus technology. . 2017-05-00. Pubmed ID: 28677531; DOI: 10.1016/j.scr.2016.09.002 WISCi004-ABCRTi005-A 2017-05-00 2017-05-00 PubMed: 28677531 DOI: 10.1016/j.scr.2016.09.002Associated cell lines:
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Saarimäki-Vire J, Balboa D, Russell MA, Saarikettu J, Kinnunen M, Keskitalo S, Malhi A, Valensisi C, Andrus C, Eurola S, Grym H, Ustinov J, Wartiovaara K, Hawkins RD, Silvennoinen O, Varjosalo M, Morgan NG, Otonkoski T
An Activating STAT3 Mutation Causes Neonatal Diabetes through Premature Induction of Pancreatic Differentiation
Saarimäki-Vire J et al. An Activating STAT3 Mutation Causes Neonatal Diabetes through Premature Induction of Pancreatic Differentiation. . 2017-04-11. Pubmed ID: 28402852; DOI: 10.1016/j.celrep.2017.03.055 UHi006-AUHi007-AULBi003-A 2017-04-11 2017-04-11 PubMed: 28402852 DOI: 10.1016/j.celrep.2017.03.055 -
Panopoulos AD, D'Antonio M, Benaglio P, Williams R, Hashem SI, Schuldt BM, DeBoever C, Arias AD, Garcia M, Nelson BC, Harismendy O, Jakubosky DA, Donovan MKR, Greenwald WW, Farnam K, Cook M, Borja V, Miller CA, Grinstein JD, Drees F, Okubo J, Diffenderfer KE, Hishida Y, Modesto V, Dargitz CT, Feiring R, Zhao C, Aguirre A, McGarry TJ, Matsui H, Li H, Reyna J, Rao F, O'Connor DT, Yeo GW, Evans SM, Chi NC, Jepsen K, Nariai N, Müller FJ, Goldstein LSB, Izpisua Belmonte JC, Adler E, Loring JF, Berggren WT, D'Antonio-Chronowska A, Smith EN, Frazer KA
iPSCORE: A Resource of 222 iPSC Lines Enabling Functional Characterization of Genetic Variation across a Variety of Cell Types
Panopoulos AD et al. iPSCORE: A Resource of 222 iPSC Lines Enabling Functional Characterization of Genetic Variation across a Variety of Cell Types. . 2017-04-11. Pubmed ID: 28410642; DOI: 10.1016/j.stemcr.2017.03.012; PMC: PMC5390244 UCSDi001-A 2017-04-11 2017-04-11 PubMed: 28410642 DOI: 10.1016/j.stemcr.2017.03.012Associated cell lines:
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Rocchetti M, Sala L, Dreizehnter L, Crotti L, Sinnecker D, Mura M, Pane LS, Altomare C, Torre E, Mostacciuolo G, Severi S, Porta A, De Ferrari GM, George AL Jr, Schwartz PJ, Gnecchi M, Moretti A, Zaza A
Elucidating arrhythmogenic mechanisms of long-QT syndrome CALM1-F142L mutation in patient-specific induced pluripotent stem cell-derived cardiomyocytes
Rocchetti M et al. Elucidating arrhythmogenic mechanisms of long-QT syndrome CALM1-F142L mutation in patient-specific induced pluripotent stem cell-derived cardiomyocytes. . 2017-04-01. Pubmed ID: 28158429; DOI: 10.1093/cvr/cvx006 MRIi011-A 2017-04-01 2017-04-01 PubMed: 28158429 DOI: 10.1093/cvr/cvx006Associated cell lines:
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Hu K, Li J, Zhu K, Chen J, Liu D, Wang Y, Sun Y, Lai H, Wang C
Generation of an induced pluripotent stem cell line from a Loeys-Dietz syndrome patient with transforming growth factor-beta receptor-2 gene mutation
Hu K et al. Generation of an induced pluripotent stem cell line from a Loeys-Dietz syndrome patient with transforming growth factor-beta receptor-2 gene mutation. . 2017-04-00. Pubmed ID: 28395736; DOI: 10.1016/j.scr.2017.03.012 FDZSi001-A 2017-04-00 2017-04-00 PubMed: 28395736 DOI: 10.1016/j.scr.2017.03.012Associated cell lines:
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Sontag S, Förster M, Qin J, Wanek P, Mitzka S, Schüler HM, Koschmieder S, Rose-John S, Seré K, Zenke M
Modelling IRF8 Deficient Human Hematopoiesis and Dendritic Cell Development with Engineered iPS Cells
Sontag S et al. Modelling IRF8 Deficient Human Hematopoiesis and Dendritic Cell Development with Engineered iPS Cells. . 2017-04-00. Pubmed ID: 28090699; DOI: 10.1002/stem.2565 ESIBIe003-AUKAi001-AUKAi001-BUKAi001-CUKAi001-A-1UKAi001-B-1UKAi001-C-1ESIBIe003-A-7 2017-04-00 2017-04-00 PubMed: 28090699 DOI: 10.1002/stem.2565Associated cell lines:
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Achuta VS, Grym H, Putkonen N, Louhivuori V, Kärkkäinen V, Koistinaho J, Roybon L, Castrén ML
Metabotropic glutamate receptor 5 responses dictate differentiation of neural progenitors to NMDA-responsive cells in fragile X syndrome
Achuta VS et al. Metabotropic glutamate receptor 5 responses dictate differentiation of neural progenitors to NMDA-responsive cells in fragile X syndrome. . 2017-04-00. Pubmed ID: 27411166; DOI: 10.1002/dneu.22419 ULBi003-AUHi007-B 2017-04-00 2017-04-00 PubMed: 27411166 DOI: 10.1002/dneu.22419 -
Phanthong P, Borwornpinyo S, Kitiyanant N, Jearawiriyapaisarn N, Nuntakarn L, Saetan J, Nualkaew T, Sa-Ngiamsuntorn K, Anurathapan U, Dinnyes A, Kitiyanant Y, Hongeng S
Enhancement of β-Globin Gene Expression in Thalassemic IVS2-654 Induced Pluripotent Stem Cell-Derived Erythroid Cells by Modified U7 snRNA
Phanthong P et al. Enhancement of β-Globin Gene Expression in Thalassemic IVS2-654 Induced Pluripotent Stem Cell-Derived Erythroid Cells by Modified U7 snRNA. . 2017-04-00. Pubmed ID: 28213976; DOI: 10.1002/sctm.16-0121; PMC: PMC5442829 MUi001-AMUi002-A 2017-04-00 2017-04-00 PubMed: 28213976 DOI: 10.1002/sctm.16-0121 -
Jung-Klawitter S, Ebersold J, Göhring G, Blau N, Opladen T
Generation of an iPSC line from a patient with GTP cyclohydrolase 1 (GCH1) deficiency: HDMC0061i-GCH1
Jung-Klawitter S et al. Generation of an iPSC line from a patient with GTP cyclohydrolase 1 (GCH1) deficiency: HDMC0061i-GCH1. . 2017-04-00. Pubmed ID: 28395739; DOI: 10.1016/j.scr.2017.02.010 DHMCi002-A 2017-04-00 2017-04-00 PubMed: 28395739 DOI: 10.1016/j.scr.2017.02.010Associated cell lines:
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Wongkummool W, Maneepitasut W, Tong-Ngam P, Tangprasittipap A, Munkongdee T, Boonchuay C, Svasti S, Kitiyanant N, Paiboonsukwong K, Fucharoen S, Tubsuwan A
Establishment of MUi009 - A human induced pluripotent stem cells from a 32year old male with homozygous β°-thalassemia coinherited with heterozygous α-thalassemia 2
Wongkummool W et al. Establishment of MUi009 - A human induced pluripotent stem cells from a 32year old male with homozygous β°-thalassemia coinherited with heterozygous α-thalassemia 2. . 2017-04-00. Pubmed ID: 28395745; DOI: 10.1016/j.scr.2017.02.012 MUi009-A 2017-04-00 2017-04-00 PubMed: 28395745 DOI: 10.1016/j.scr.2017.02.012Associated cell lines:
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Wongkummool W, Maneepitasut W, Munkongdee T, Tong-Ngam P, Tangprasittipap A, Svasti S, Kitiyanant N, Paiboonsukwong K, Fucharoen S, Tubsuwan A
Derivation of the human induced pluripotent stem cell line MUi017-A from a patient with homozygous Hemoglobin Constant Spring
Wongkummool W et al. Derivation of the human induced pluripotent stem cell line MUi017-A from a patient with homozygous Hemoglobin Constant Spring. . 2017-04-00. Pubmed ID: 28395746; DOI: 10.1016/j.scr.2017.02.014 MUi017-A 2017-04-00 2017-04-00 PubMed: 28395746 DOI: 10.1016/j.scr.2017.02.014Associated cell lines:
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Tangprasittipap A, Jittorntrum B, Wongkummool W, Kitiyanant N, Tubsuwan A
Generation of induced pluripotent stem cells from peripheral blood CD34+ hematopoietic progenitors of a 31year old healthy woman
Tangprasittipap A et al. Generation of induced pluripotent stem cells from peripheral blood CD34+ hematopoietic progenitors of a 31year old healthy woman. . 2017-04-00. Pubmed ID: 28395748; DOI: 10.1016/j.scr.2017.02.013 MUi019-A 2017-04-00 2017-04-00 PubMed: 28395748 DOI: 10.1016/j.scr.2017.02.013Associated cell lines:
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Yang CT, Ma R, Axton RA, Jackson M, Taylor AH, Fidanza A, Marenah L, Frayne J, Mountford JC, Forrester LM
Activation of KLF1 Enhances the Differentiation and Maturation of Red Blood Cells from Human Pluripotent Stem Cells
Yang CT et al. Activation of KLF1 Enhances the Differentiation and Maturation of Red Blood Cells from Human Pluripotent Stem Cells. . 2017-04-00. Pubmed ID: 28026072; DOI: 10.1002/stem.2562; PMC: PMC5396323 EDi020-A 2017-04-00 2017-04-00 PubMed: 28026072 DOI: 10.1002/stem.2562Associated cell lines:
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Lach MS, Wroblewska JP, Augustyniak E, Kulcenty K, Suchorska WM
A feeder- and xeno-free human induced pluripotent stem cell line obtained from primary human dermal fibroblasts with epigenetic repression of reprogramming factors expression: GPCCi001-A
Lach MS et al. A feeder- and xeno-free human induced pluripotent stem cell line obtained from primary human dermal fibroblasts with epigenetic repression of reprogramming factors expression: GPCCi001-A. . 2017-04-00. Pubmed ID: 28395738; DOI: 10.1016/j.scr.2017.02.004 GPCCi001-A 2017-04-00 2017-04-00 PubMed: 28395738 DOI: 10.1016/j.scr.2017.02.004Associated cell lines:
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De Sousa PA, Steeg R, Wachter E, Bruce K, King J, Hoeve M, Khadun S, McConnachie G, Holder J, Kurtz A, Seltmann S, Dewender J, Reimann S, Stacey G, O'Shea O, Chapman C, Healy L, Zimmermann H, Bolton B, Rawat T, Atkin I, Veiga A, Kuebler B, Serano BM, Saric T, Hescheler J, Brüstle O, Peitz M, Thiele C, Geijsen N, Holst B, Clausen C, Lako M, Armstrong L, Gupta SK, Kvist AJ, Hicks R, Jonebring A, Brolén G, Ebneth A, Cabrera-Socorro A, Foerch P, Geraerts M, Stummann TC, Harmon S, George C, Streeter I, Clarke L, Parkinson H, Harrison PW, Faulconbridge A, Cherubin L, Burdett T, Trigueros C, Patel MJ, Lucas C, Hardy B, Predan R, Dokler J, Brajnik M, Keminer O, Pless O, Gribbon P, Claussen C, Ringwald A, Kreisel B, Courtney A, Allsopp TE
Rapid establishment of the European Bank for induced Pluripotent Stem Cells (EBiSC) - the Hot Start experience
De Sousa PA et al. Rapid establishment of the European Bank for induced Pluripotent Stem Cells (EBiSC) - the Hot Start experience. . 2017-04-00. Pubmed ID: 28334554; DOI: 10.1016/j.scr.2017.03.002 UKBi005-A 2017-04-00 2017-04-00 PubMed: 28334554 DOI: 10.1016/j.scr.2017.03.002Associated cell lines:
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Ayllón V, Vogel-González M, González-Pozas F, Domingo-Reinés J, Montes R, Morales-Cacho L, Ramos-Mejía V
New hPSC-based human models to study pediatric Acute Megakaryoblastic Leukemia harboring the fusion oncogene RBM15-MKL1
Ayllón V et al. New hPSC-based human models to study pediatric Acute Megakaryoblastic Leukemia harboring the fusion oncogene RBM15-MKL1. . 2017-03-00. Pubmed ID: 28412998; DOI: 10.1016/j.scr.2016.12.019 WAe009-A-5GENYOi003-A 2017-03-00 2017-03-00 PubMed: 28412998 DOI: 10.1016/j.scr.2016.12.019Associated cell lines:
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Rodriguez-Muela N, Litterman NK, Norabuena EM, Mull JL, Galazo MJ, Sun C, Ng SY, Makhortova NR, White A, Lynes MM, Chung WK, Davidow LS, Macklis JD, Rubin LL
Single-Cell Analysis of SMN Reveals Its Broader Role in Neuromuscular Disease
Rodriguez-Muela N et al. Single-Cell Analysis of SMN Reveals Its Broader Role in Neuromuscular Disease. . 2017-02-07. Pubmed ID: 28178525; DOI: 10.1016/j.celrep.2017.01.035; PMC: PMC5463539 HVRDi005-AHVRDi015-AHVRDi016-AHVRDi017-A 2017-02-07 2017-02-07 PubMed: 28178525 DOI: 10.1016/j.celrep.2017.01.035Associated cell lines:
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Sandor C, Robertson P, Lang C, Heger A, Booth H, Vowles J, Witty L, Bowden R, Hu M, Cowley SA, Wade-Martins R, Webber C
Transcriptomic profiling of purified patient-derived dopamine neurons identifies convergent perturbations and therapeutics for Parkinson's disease
Sandor C et al. Transcriptomic profiling of purified patient-derived dopamine neurons identifies convergent perturbations and therapeutics for Parkinson's disease. . 2017-02-01. Pubmed ID: 28096185; DOI: 10.1093/hmg/ddw412; PMC: PMC5409122 UOXFi004-BUOXFi007-AUOXFi008-B 2017-02-01 2017-02-01 PubMed: 28096185 DOI: 10.1093/hmg/ddw412Associated cell lines:
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Alasoo Kaur, Rodrigues Julia, Mukhopadhyay Subhankar, Knights Andrew J., Mann Alice L., Kundu Kousik, Hale Christine, Dougan Gordon, Gaffney Daniel J.
Shared genetic effects on chromatin and gene expression reveal widespread enhancer priming in immune response
Alasoo Kaur et al. Shared genetic effects on chromatin and gene expression reveal widespread enhancer priming in immune response. . 2017-01-26. DOI: 10.1101/102392 WTSIi362-B 2017-01-26 2017-01-26 DOI: 10.1101/102392Associated cell lines:
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Schwartzentruber Jeremy, Foskolou Stefanie, Kilpinen Helena, Rodrigues Julia, Alasoo Kaur, Knights Andrew J, Patel Minal, Goncalves Angela, Ferreira Rita, Benn Caroline Louise, Wilbrey Anna, Bictash Magda, Impey Emma, Cao Lishuang, Lainez Sergio, Loucif Alexandre Julien, Whiting Paul John, Gutteridge Alex, Gaffney Daniel J
Molecular and functional variation in iPSC-derived sensory neurons
Schwartzentruber Jeremy et al. Molecular and functional variation in iPSC-derived sensory neurons. . 2017-01-06. DOI: 10.1101/095943 WTSIi089-B 2017-01-06 2017-01-06 DOI: 10.1101/095943Associated cell lines:
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Kirkeby A, Nolbrant S, Tiklova K, Heuer A, Kee N, Cardoso T, Ottosson DR, Lelos MJ, Rifes P, Dunnett SB, Grealish S, Perlmann T, Parmar M
Predictive Markers Guide Differentiation to Improve Graft Outcome in Clinical Translation of hESC-Based Therapy for Parkinson's Disease
Kirkeby A et al. Predictive Markers Guide Differentiation to Improve Graft Outcome in Clinical Translation of hESC-Based Therapy for Parkinson's Disease. . 2017-01-05. Pubmed ID: 28094017; DOI: 10.1016/j.stem.2016.09.004; PMC: PMC5222722 RCe021-A 2017-01-05 2017-01-05 PubMed: 28094017 DOI: 10.1016/j.stem.2016.09.004Associated cell lines:
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Rehakova D.
Standardized hiPSCs culture – vitronectin coating for cGMP compliant protocol
Rehakova D.. Standardized hiPSCs culture – vitronectin coating for cGMP compliant protocol. . 2017-01-01. CSCRMi001-A 2017-01-01 2017-01-01Associated cell lines:
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Acquaviva F, Sana ME, Della Monica M, Pinelli M, Postorivo D, Fontana P, Falco MT, Nardone AM, Lonardo F, Iascone M, Scarano G
First evidence of Smith-Magenis syndrome in mother and daughter due to a novel RAI mutation
Acquaviva F et al. First evidence of Smith-Magenis syndrome in mother and daughter due to a novel RAI mutation. . 2017-01-00. Pubmed ID: 27683195; DOI: 10.1002/ajmg.a.37989 CSSi003-A 2017-01-00 2017-01-00 PubMed: 27683195 DOI: 10.1002/ajmg.a.37989Associated cell lines:
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Uhlin E, Rönnholm H, Day K, Kele M, Tammimies K, Bölte S, Falk A
Derivation of human iPS cell lines from monozygotic twins in defined and xeno free conditions
Uhlin E et al. Derivation of human iPS cell lines from monozygotic twins in defined and xeno free conditions. . 2017-01-00. Pubmed ID: 28395796; DOI: 10.1016/j.scr.2016.12.006 KICRi002-A 2017-01-00 2017-01-00 PubMed: 28395796 DOI: 10.1016/j.scr.2016.12.006Associated cell lines:
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Kuusela J, Kim J, Räsänen E, Aalto-Setälä K
The Effects of Pharmacological Compounds on Beat Rate Variations in Human Long QT-Syndrome Cardiomyocytes
Kuusela J et al. The Effects of Pharmacological Compounds on Beat Rate Variations in Human Long QT-Syndrome Cardiomyocytes. . 2016-12-00. Pubmed ID: 27646833; DOI: 10.1007/s12015-016-9686-0; PMC: PMC5106508 TAUi002-ATAUi007-ATAUi007-B 2016-12-00 2016-12-00 PubMed: 27646833 DOI: 10.1007/s12015-016-9686-0 -
Bruce KW, Campbell JD, De Sousa P
Quality Assured Characterization of Stem Cells for Safety in Banking for Clinical Application
Bruce KW et al. Quality Assured Characterization of Stem Cells for Safety in Banking for Clinical Application. . 2017-00-00. Pubmed ID: 28353263; DOI: 10.1007/978-1-4939-6921-0_6 RCe013-A 2017-00-00 2017-00-00 PubMed: 28353263 DOI: 10.1007/978-1-4939-6921-0_6Associated cell lines:
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Hunt CJ
Cryopreservation: Vitrification and Controlled Rate Cooling
Hunt CJ. Cryopreservation: Vitrification and Controlled Rate Cooling. . 2017-00-00. Pubmed ID: 28353262; DOI: 10.1007/978-1-4939-6921-0_5 RCe016-A 2017-00-00 2017-00-00 PubMed: 28353262 DOI: 10.1007/978-1-4939-6921-0_5Associated cell lines:
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Baker D, Hirst AJ, Gokhale PJ, Juarez MA, Williams S, Wheeler M, Bean K, Allison TF, Moore HD, Andrews PW, Barbaric I
Detecting Genetic Mosaicism in Cultures of Human Pluripotent Stem Cells
Baker D et al. Detecting Genetic Mosaicism in Cultures of Human Pluripotent Stem Cells. . 2016-11-08. Pubmed ID: 27829140; DOI: 10.1016/j.stemcr.2016.10.003; PMC: PMC5106530 AXORe005-AUOSe013-AUOSe018-A 2016-11-08 2016-11-08 PubMed: 27829140 DOI: 10.1016/j.stemcr.2016.10.003Associated cell lines:
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Xu C, Zhang Y, Wang Q, Xu Z, Jiang J, Gao Y, Gao M, Kang J, Wu M, Xiong J, Ji K, Yuan W, Wang Y, Liu H
Long non-coding RNA GAS5 controls human embryonic stem cell self-renewal by maintaining NODAL signalling
Xu C et al. Long non-coding RNA GAS5 controls human embryonic stem cell self-renewal by maintaining NODAL signalling. . 2016-11-04. Pubmed ID: 27811843; DOI: 10.1038/ncomms13287; PMC: PMC5097163 WAe001-AWAe009-A 2016-11-04 2016-11-04 PubMed: 27811843 DOI: 10.1038/ncomms13287 -
Ishida Y, Kawakami H, Kitajima H, Nishiyama A, Sasai Y, Inoue H, Muguruma K
Vulnerability of Purkinje Cells Generated from Spinocerebellar Ataxia Type 6 Patient-Derived iPSCs
Ishida Y et al. Vulnerability of Purkinje Cells Generated from Spinocerebellar Ataxia Type 6 Patient-Derived iPSCs. . 2016-11-01. Pubmed ID: 27806289; DOI: 10.1016/j.celrep.2016.10.026 KUIFMSi004-C 2016-11-01 2016-11-01 PubMed: 27806289 DOI: 10.1016/j.celrep.2016.10.026Associated cell lines:
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Nimsanor N, Kitiyanant N, Poulsen U, Rasmussen MA, Clausen C, Mau-Holzmann UA, Nielsen JE, Nielsen TT, Hyttel P, Holst B, Schmid B
Generation of an isogenic, gene-corrected iPSC line from a symptomatic 57-year-old female patient with frontotemporal dementia caused by a P301L mutation in the microtubule associated protein tau (MAPT) gene
Nimsanor N et al. Generation of an isogenic, gene-corrected iPSC line from a symptomatic 57-year-old female patient with frontotemporal dementia caused by a P301L mutation in the microtubule associated protein tau (MAPT) gene. . 2016-11-00. Pubmed ID: 27789409; DOI: 10.1016/j.scr.2016.09.021 BIONi010-C 2016-11-00 2016-11-00 PubMed: 27789409 DOI: 10.1016/j.scr.2016.09.021Associated cell lines:
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Skrzypczyk A, Giri S, Bader A
Generation of induced pluripotent stem cell line from foreskin fibroblasts
Skrzypczyk A et al. Generation of induced pluripotent stem cell line from foreskin fibroblasts. . 2016-11-00. Pubmed ID: 27789413; DOI: 10.1016/j.scr.2016.09.014 ULEIi001-A 2016-11-00 2016-11-00 PubMed: 27789413 DOI: 10.1016/j.scr.2016.09.014Associated cell lines:
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Nimsanor N, Poulsen U, Rasmussen MA, Clausen C, Mau-Holzmann UA, Nielsen JE, Nielsen TT, Hyttel P, Holst B, Schmid B
Generation of an isogenic, gene-corrected iPSC line from a pre-symptomatic 28-year-old woman with an R406W mutation in the microtubule associated protein tau (MAPT) gene
Nimsanor N et al. Generation of an isogenic, gene-corrected iPSC line from a pre-symptomatic 28-year-old woman with an R406W mutation in the microtubule associated protein tau (MAPT) gene. . 2016-11-00. Pubmed ID: 27934590; DOI: 10.1016/j.scr.2016.09.024 BIONi010-C 2016-11-00 2016-11-00 PubMed: 27934590 DOI: 10.1016/j.scr.2016.09.024Associated cell lines:
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Nimsanor N, Jørring I, Rasmussen MA, Clausen C, Mau-Holzmann UA, Bus C, Hoffmann SA, Gasser T, Kluba T, Holst B, Schmid B
Generation of induced pluripotent stem cells derived from a 77-year-old healthy woman as control for age related diseases
Nimsanor N et al. Generation of induced pluripotent stem cells derived from a 77-year-old healthy woman as control for age related diseases. . 2016-11-00. Pubmed ID: 27789407; DOI: 10.1016/j.scr.2016.09.019 BIONi010-CBIONi037-A 2016-11-00 2016-11-00 PubMed: 27789407 DOI: 10.1016/j.scr.2016.09.019Associated cell lines:
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Nimsanor N, Poulsen U, Rasmussen MA, Clausen C, Mau-Holzmann UA, Nielsen JE, Nielsen TT, Hyttel P, Holst B, Schmid B
Generation of an isogenic, gene-corrected iPSC line from a symptomatic 59-year-old female patient with frontotemporal dementia caused by an R406W mutation in the microtubule associated protein tau (MAPT) gene
Nimsanor N et al. Generation of an isogenic, gene-corrected iPSC line from a symptomatic 59-year-old female patient with frontotemporal dementia caused by an R406W mutation in the microtubule associated protein tau (MAPT) gene. . 2016-11-00. Pubmed ID: 27934586; DOI: 10.1016/j.scr.2016.09.020 BIONi010-C 2016-11-00 2016-11-00 PubMed: 27934586 DOI: 10.1016/j.scr.2016.09.020Associated cell lines:
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Jung-Klawitter S, Blau N, Sebe A, Ebersold J, Göhring G, Opladen T
Generation of an iPSC line from a patient with tyrosine hydroxylase (TH) deficiency: TH-1 iPSC
Jung-Klawitter S et al. Generation of an iPSC line from a patient with tyrosine hydroxylase (TH) deficiency: TH-1 iPSC. . 2016-11-00. Pubmed ID: 27934587; DOI: 10.1016/j.scr.2016.10.008 DHMCi001-A 2016-11-00 2016-11-00 PubMed: 27934587 DOI: 10.1016/j.scr.2016.10.008Associated cell lines:
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Nimsanor N, Jørring I, Rasmussen MA, Clausen C, Mau-Holzmann UA, Kitiyanant N, Nielsen JE, Nielsen TT, Hyttel P, Holst B, Schmid B
Induced pluripotent stem cells (iPSCs) derived from a symptomatic carrier of a S305I mutation in the microtubule-associated protein tau (MAPT)-gene causing frontotemporal dementia
Nimsanor N et al. Induced pluripotent stem cells (iPSCs) derived from a symptomatic carrier of a S305I mutation in the microtubule-associated protein tau (MAPT)-gene causing frontotemporal dementia. . 2016-11-00. Pubmed ID: 27789411; DOI: 10.1016/j.scr.2016.10.006 BIONi010-C 2016-11-00 2016-11-00 PubMed: 27789411 DOI: 10.1016/j.scr.2016.10.006Associated cell lines:
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Tofoli FA, Dasso M, Morato-Marques M, Nunes K, Pereira LA, da Silva GS, Fonseca SA, Costas RM, Santos HC, da Costa Pereira A, Lotufo PA, Bensenor IM, Meyer D, Pereira LV
Increasing The Genetic Admixture of Available Lines of Human Pluripotent Stem Cells
Tofoli FA et al. Increasing The Genetic Admixture of Available Lines of Human Pluripotent Stem Cells. . 2016-10-06. Pubmed ID: 27708369; DOI: 10.1038/srep34699; PMC: PMC5052616 LANCEi020-A 2016-10-06 2016-10-06 PubMed: 27708369 DOI: 10.1038/srep34699Associated cell lines:
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Mor-Shaked H, Eiges R
Modeling Fragile X Syndrome Using Human Pluripotent Stem Cells
Mor-Shaked H et al. Modeling Fragile X Syndrome Using Human Pluripotent Stem Cells. . 2016-09-28. Pubmed ID: 27690107; DOI: 10.3390/genes7100077; PMC: PMC5083916 VUBe011-AVUBe012-AHADe005-AVUBe013-ARGIe116-AINSRMe002-AINSRMe005-A 2016-09-28 2016-09-28 PubMed: 27690107 DOI: 10.3390/genes7100077Associated cell lines:
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Sugai K, Fukuzawa R, Shofuda T, Fukusumi H, Kawabata S, Nishiyama Y, Higuchi Y, Kawai K, Isoda M, Kanematsu D, Hashimoto-Tamaoki T, Kohyama J, Iwanami A, Suemizu H, Ikeda E, Matsumoto M, Kanemura Y, Nakamura M, Okano H
Pathological classification of human iPSC-derived neural stem/progenitor cells towards safety assessment of transplantation therapy for CNS diseases
Sugai K et al. Pathological classification of human iPSC-derived neural stem/progenitor cells towards safety assessment of transplantation therapy for CNS diseases. . 2016-09-19. Pubmed ID: 27642008; DOI: 10.1186/s13041-016-0265-8; PMC: PMC5027634 KUIMSi012-A 2016-09-19 2016-09-19 PubMed: 27642008 DOI: 10.1186/s13041-016-0265-8Associated cell lines:
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Nishizawa M, Chonabayashi K, Nomura M, Tanaka A, Nakamura M, Inagaki A, Nishikawa M, Takei I, Oishi A, Tanabe K, Ohnuki M, Yokota H, Koyanagi-Aoi M, Okita K, Watanabe A, Takaori-Kondo A, Yamanaka S, Yoshida Y
Epigenetic Variation between Human Induced Pluripotent Stem Cell Lines Is an Indicator of Differentiation Capacity
Nishizawa M et al. Epigenetic Variation between Human Induced Pluripotent Stem Cell Lines Is an Indicator of Differentiation Capacity. . 2016-09-01. Pubmed ID: 27476965; DOI: 10.1016/j.stem.2016.06.019 WAe001-AWAe009-AKUIMSe001-AKUIMSe003-AKUIFMSi004-BKUIFMSi004-CKUIFMSi011-ACIRAi007-A 2016-09-01 2016-09-01 PubMed: 27476965 DOI: 10.1016/j.stem.2016.06.019Associated cell lines:
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Rossbach B, Hildebrand L, El-Ahmad L, Stachelscheid H, Reinke P, Kurtz A
Corrigendum to "Generation of a human induced pluripotent stem cell line from urinary cells of a healthy donor using an integration free vector" [Stem Cell Res. 16/2 (2016) 314-317]
Rossbach B et al. Corrigendum to "Generation of a human induced pluripotent stem cell line from urinary cells of a healthy donor using an integration free vector" [Stem Cell Res. 16/2 (2016) 314-317]. . 2016-09-00. Pubmed ID: 27638042; DOI: 10.1016/j.scr.2016.09.003 BCRTi004-A 2016-09-00 2016-09-00 PubMed: 27638042 DOI: 10.1016/j.scr.2016.09.003Associated cell lines:
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Hansen SK, Stummann TC, Borland H, Hasholt LF, Tümer Z, Nielsen JE, Rasmussen MA, Nielsen TT, Daechsel JC, Fog K, Hyttel P
Induced pluripotent stem cell - derived neurons for the study of spinocerebellar ataxia type 3
Hansen SK et al. Induced pluripotent stem cell - derived neurons for the study of spinocerebellar ataxia type 3. . 2016-09-00. Pubmed ID: 27596958; DOI: 10.1016/j.scr.2016.07.004 BIONi010-ABIONi010-BBIONi010-C 2016-09-00 2016-09-00 PubMed: 27596958 DOI: 10.1016/j.scr.2016.07.004Associated cell lines:
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Caron L, Kher D, Lee KL, McKernan R, Dumevska B, Hidalgo A, Li J, Yang H, Main H, Ferri G, Petek LM, Poellinger L, Miller DG, Gabellini D, Schmidt U
A Human Pluripotent Stem Cell Model of Facioscapulohumeral Muscular Dystrophy-Affected Skeletal Muscles
Caron L et al. A Human Pluripotent Stem Cell Model of Facioscapulohumeral Muscular Dystrophy-Affected Skeletal Muscles. . 2016-09-00. Pubmed ID: 27217344; DOI: 10.5966/sctm.2015-0224; PMC: PMC4996435 GENEAe020-A 2016-09-00 2016-09-00 PubMed: 27217344 DOI: 10.5966/sctm.2015-0224Associated cell lines:
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Jung HS, Uenishi G, Kumar A, Park MA, Raymond M, Fink D, McLeod E, Slukvin I
A human VE-cadherin-tdTomato and CD43-green fluorescent protein dual reporter cell line for study endothelial to hematopoietic transition
Jung HS et al. A human VE-cadherin-tdTomato and CD43-green fluorescent protein dual reporter cell line for study endothelial to hematopoietic transition. . 2016-09-00. Pubmed ID: 27879215; DOI: 10.1016/j.scr.2016.09.004; PMC: PMC5123598 WAe001-A-80 2016-09-00 2016-09-00 PubMed: 27879215 DOI: 10.1016/j.scr.2016.09.004Associated cell lines:
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De Sousa PA, Downie JM, Tye BJ, Bruce K, Dand P, Dhanjal S, Serhal P, Harper J, Turner M, Bateman M
Development and production of good manufacturing practice grade human embryonic stem cell lines as source material for clinical application
De Sousa PA et al. Development and production of good manufacturing practice grade human embryonic stem cell lines as source material for clinical application. . 2016-09-00. Pubmed ID: 27639108; DOI: 10.1016/j.scr.2016.08.011 RCe006-ARCe007-ARCe008-ARCe009-ARCe010-ARCe011-ARCe012-ARCe013-ARCe014-ARCe015-ARCe016-ARCe017-ARCe018-ARCe019-ARCe020-ARCe021-A 2016-09-00 2016-09-00 PubMed: 27639108 DOI: 10.1016/j.scr.2016.08.011 -
Sala L, Yu Z, Ward-van Oostwaard D, van Veldhoven JP, Moretti A, Laugwitz KL, Mummery CL, IJzerman AP, Bellin M
A new hERG allosteric modulator rescues genetic and drug-induced long-QT syndrome phenotypes in cardiomyocytes from isogenic pairs of patient induced pluripotent stem cells
Sala L et al. A new hERG allosteric modulator rescues genetic and drug-induced long-QT syndrome phenotypes in cardiomyocytes from isogenic pairs of patient induced pluripotent stem cells. . 2016-09-00. Pubmed ID: 27470144; DOI: 10.15252/emmm.201606260; PMC: PMC5009811 LUMCi039-A 2016-09-00 2016-09-00 PubMed: 27470144 DOI: 10.15252/emmm.201606260Associated cell lines:
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Mathapati S, Siller R, Impellizzeri AA, Lycke M, Vegheim K, Almaas R, Sullivan GJ
Small-Molecule-Directed Hepatocyte-Like Cell Differentiation of Human Pluripotent Stem Cells
Mathapati S et al. Small-Molecule-Directed Hepatocyte-Like Cell Differentiation of Human Pluripotent Stem Cells. . 2016-08-17. Pubmed ID: 27532814; DOI: 10.1002/cpsc.13 UIOi001-A 2016-08-17 2016-08-17 PubMed: 27532814 DOI: 10.1002/cpsc.13Associated cell lines:
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Veerman CC, Mengarelli I, Guan K, Stauske M, Barc J, Tan HL, Wilde AA, Verkerk AO, Bezzina CR
hiPSC-derived cardiomyocytes from Brugada Syndrome patients without identified mutations do not exhibit clear cellular electrophysiological abnormalities
Veerman CC et al. hiPSC-derived cardiomyocytes from Brugada Syndrome patients without identified mutations do not exhibit clear cellular electrophysiological abnormalities. . 2016-08-03. Pubmed ID: 27485484; DOI: 10.1038/srep30967; PMC: PMC4971529 UMGi046-AUMGi047-AUMGi048-A 2016-08-03 2016-08-03 PubMed: 27485484 DOI: 10.1038/srep30967 -
Kiselev A, Mikhaylov E, Parmon E, Sjoberg G, Sejersen T, Tarnovskaya S, Nugnyi P, Mitrofanova L, Lebedev D, Kostareva A
Progressive cardiac conduction disease associated with a DSP gene mutation
Kiselev A et al. Progressive cardiac conduction disease associated with a DSP gene mutation. . 2016-08-01. Pubmed ID: 27166992; DOI: 10.1016/j.ijcard.2016.04.164 FAMRCi004-AFAMRCi004-B 2016-08-01 2016-08-01 PubMed: 27166992 DOI: 10.1016/j.ijcard.2016.04.164Associated cell lines:
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Gerami-Naini B, Smith A, Maione AG, Kashpur O, Carpinito G, Veves A, Mooney DJ, Garlick JA
Generation of Induced Pluripotent Stem Cells from Diabetic Foot Ulcer Fibroblasts Using a Nonintegrative Sendai Virus
Gerami-Naini B et al. Generation of Induced Pluripotent Stem Cells from Diabetic Foot Ulcer Fibroblasts Using a Nonintegrative Sendai Virus. . 2016-08-00. Pubmed ID: 27328415; DOI: 10.1089/cell.2015.0087; PMC: PMC4964760 RCSIi002-ARCSIi003-ARCSIi004-ARCSIi005-A 2016-08-00 2016-08-00 PubMed: 27328415 DOI: 10.1089/cell.2015.0087Associated cell lines:
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Heuer A, Kirkeby A, Pfisterer U, Jönsson ME, Parmar M
hESC-derived neural progenitors prevent xenograft rejection through neonatal desensitisation
Heuer A et al. hESC-derived neural progenitors prevent xenograft rejection through neonatal desensitisation. . 2016-08-00. Pubmed ID: 27235932; DOI: 10.1016/j.expneurol.2016.05.027; PMC: PMC4920671 RCe021-A 2016-08-00 2016-08-00 PubMed: 27235932 DOI: 10.1016/j.expneurol.2016.05.027Associated cell lines:
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Salomonis N, Dexheimer PJ, Omberg L, Schroll R, Bush S, Huo J, Schriml L, Ho Sui S, Keddache M, Mayhew C, Shanmukhappa SK, Wells J, Daily K, Hubler S, Wang Y, Zambidis E, Margolin A, Hide W, Hatzopoulos AK, Malik P, Cancelas JA, Aronow BJ, Lutzko C
Integrated Genomic Analysis of Diverse Induced Pluripotent Stem Cells from the Progenitor Cell Biology Consortium
Salomonis N et al. Integrated Genomic Analysis of Diverse Induced Pluripotent Stem Cells from the Progenitor Cell Biology Consortium. . 2016-07-12. Pubmed ID: 27293150; DOI: 10.1016/j.stemcr.2016.05.006; PMC: PMC4944587 WAe007-AWAe009-ABCHe002-ATMOi001-AWAi001-BWAi001-CUMNi001-AWAe024-A 2016-07-12 2016-07-12 PubMed: 27293150 DOI: 10.1016/j.stemcr.2016.05.006 -
De Sousa PA, Tye BJ, Bruce K, Dand P, Russell G, Collins DM, Greenshields A, McDonald K, Bradburn H, Canham MA, Kunath T, Downie JM, Bateman M, Courtney A
Derivation of the clinical grade human embryonic stem cell line RCe013-A (RC-9)
De Sousa PA et al. Derivation of the clinical grade human embryonic stem cell line RCe013-A (RC-9). . 2016-07-00. Pubmed ID: 27558601; DOI: 10.1016/j.scr.2016.04.020 RCe013-A 2016-07-00 2016-07-00 PubMed: 27558601 DOI: 10.1016/j.scr.2016.04.020Associated cell lines:
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Lenzi J, Pagani F, De Santis R, Limatola C, Bozzoni I, Di Angelantonio S, Rosa A
Differentiation of control and ALS mutant human iPSCs into functional skeletal muscle cells, a tool for the study of neuromuscolar diseases
Lenzi J et al. Differentiation of control and ALS mutant human iPSCs into functional skeletal muscle cells, a tool for the study of neuromuscolar diseases. . 2016-07-00. Pubmed ID: 27318155; DOI: 10.1016/j.scr.2016.06.003; PMC: PMC5009183 SAPi002-ASAPi003-ASAPi004-A 2016-07-00 2016-07-00 PubMed: 27318155 DOI: 10.1016/j.scr.2016.06.003 -
De Sousa PA, Tye BJ, Bruce K, Dand P, Russell G, Collins DM, Greenshields A, McDonald K, Bradburn H, Laurie A, Canham M, Kunath T, Downie JM, Bateman M, Courtney A
Derivation of the clinical grade human embryonic stem cell line RCe015-A (RC-11)
De Sousa PA et al. Derivation of the clinical grade human embryonic stem cell line RCe015-A (RC-11). . 2016-07-00. Pubmed ID: 27558602; DOI: 10.1016/j.scr.2016.04.021 RCe015-A 2016-07-00 2016-07-00 PubMed: 27558602 DOI: 10.1016/j.scr.2016.04.021Associated cell lines:
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Nemes C, Varga E, Táncos Z, Bock I, Francz B, Kobolák J, Dinnyés A
Establishment of PSEN1 mutant induced pluripotent stem cell (iPSC) line from an Alzheimer's disease (AD) female patient
Nemes C et al. Establishment of PSEN1 mutant induced pluripotent stem cell (iPSC) line from an Alzheimer's disease (AD) female patient. . 2016-07-00. Pubmed ID: 27558604; DOI: 10.1016/j.scr.2016.05.019 BIOTi001-A 2016-07-00 2016-07-00 PubMed: 27558604 DOI: 10.1016/j.scr.2016.05.019Associated cell lines:
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De Sousa PA, Tye BJ, Bruce K, Dand P, Russell G, Collins DM, Greenshields A, McDonald K, Bradburn H, Allan D, Laurie A, Kunath T, Canham MA, Downie JM, Bateman M, Courtney A
Derivation of the clinical grade human embryonic stem cell line RCe021-A (RC-17)
De Sousa PA et al. Derivation of the clinical grade human embryonic stem cell line RCe021-A (RC-17). . 2016-07-00. Pubmed ID: 27558596; DOI: 10.1016/j.scr.2016.04.019 RCe021-A 2016-07-00 2016-07-00 PubMed: 27558596 DOI: 10.1016/j.scr.2016.04.019Associated cell lines:
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Millman JR, Xie C, Van Dervort A, Gürtler M, Pagliuca FW, Melton DA
Generation of stem cell-derived β-cells from patients with type 1 diabetes
Millman JR et al. Generation of stem cell-derived β-cells from patients with type 1 diabetes. . 2016-05-10. Pubmed ID: 27163171; DOI: 10.1038/ncomms11463; PMC: PMC4866045 HVRDi007-A 2016-05-10 2016-05-10 PubMed: 27163171 DOI: 10.1038/ncomms11463Associated cell lines:
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Pei Y, Peng J, Behl M, Sipes NS, Shockley KR, Rao MS, Tice RR, Zeng X
Comparative neurotoxicity screening in human iPSC-derived neural stem cells, neurons and astrocytes
Pei Y et al. Comparative neurotoxicity screening in human iPSC-derived neural stem cells, neurons and astrocytes. . 2016-05-01. Pubmed ID: 26254731; DOI: 10.1016/j.brainres.2015.07.048; PMC: PMC5032144 CRMi003-A-1 2016-05-01 2016-05-01 PubMed: 26254731 DOI: 10.1016/j.brainres.2015.07.048Associated cell lines:
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Hansen SK, Borland H, Hasholt LF, Tümer Z, Nielsen JE, Rasmussen MA, Nielsen TT, Stummann TC, Fog K, Hyttel P
Generation of spinocerebellar ataxia type 3 patient-derived induced pluripotent stem cell line SCA3.A11
Hansen SK et al. Generation of spinocerebellar ataxia type 3 patient-derived induced pluripotent stem cell line SCA3.A11. . 2016-05-00. Pubmed ID: 27346190; DOI: 10.1016/j.scr.2016.02.040 BIONi010-B 2016-05-00 2016-05-00 PubMed: 27346190 DOI: 10.1016/j.scr.2016.02.040Associated cell lines:
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De Sousa PA, Tye BJ, Bruce K, Dand P, Russell G, Collins DM, Greenshields A, McDonald K, Bradburn H, Laurie A, Downie JM, Bateman M, Courtney A
Derivation of the clinical grade human embryonic stem cell line RCe020-a (RC-16)
De Sousa PA et al. Derivation of the clinical grade human embryonic stem cell line RCe020-a (RC-16). . 2016-05-00. Pubmed ID: 27346205; DOI: 10.1016/j.scr.2016.04.002 RCe020-A 2016-05-00 2016-05-00 PubMed: 27346205 DOI: 10.1016/j.scr.2016.04.002Associated cell lines:
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De Sousa PA, Tye BJ, Bruce K, Dand P, Russell G, Collins DM, Greenshields A, McDonald K, Bradburn H, Laurie A, Downie JM, Bateman M, Courtney A
Derivation of the clinical grade human embryonic stem cell line RCe017-A (RC-13)
De Sousa PA et al. Derivation of the clinical grade human embryonic stem cell line RCe017-A (RC-13). . 2016-05-00. Pubmed ID: 27346201; DOI: 10.1016/j.scr.2016.04.006 RCe017-A 2016-05-00 2016-05-00 PubMed: 27346201 DOI: 10.1016/j.scr.2016.04.006Associated cell lines:
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De Sousa PA, Tye BJ, Bruce K, Dand P, Russell G, Collins DM, Greenshields A, McDonald K, Bradburn H, Laurie A, Downie JM, Bateman M, Courtney A
Derivation of the clinical grade human embryonic stem cell line RCe018-A (RC-14)
De Sousa PA et al. Derivation of the clinical grade human embryonic stem cell line RCe018-A (RC-14). . 2016-05-00. Pubmed ID: 27346202; DOI: 10.1016/j.scr.2016.04.004 RCe018-A 2016-05-00 2016-05-00 PubMed: 27346202 DOI: 10.1016/j.scr.2016.04.004Associated cell lines:
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De Sousa PA, Tye BJ, Bruce K, Dand P, Russell G, Collins DM, Greenshields A, McDonald K, Bradburn H, Laurie A, Downie JM, Bateman M, Courtney A
Derivation of the clinical grade human embryonic stem cell line RCe019-A (RC-15)
De Sousa PA et al. Derivation of the clinical grade human embryonic stem cell line RCe019-A (RC-15). . 2016-05-00. Pubmed ID: 27346200; DOI: 10.1016/j.scr.2016.04.003 RCe018-ARCe019-A 2016-05-00 2016-05-00 PubMed: 27346200 DOI: 10.1016/j.scr.2016.04.003 -
De Sousa PA, Tye B, Bruce K, Dand P, Russell G, Gardner J, Downie JM, Bateman M, Courtney A
Derivation of the human embryonic stem cell line RCe007-A (RC-3)
De Sousa PA et al. Derivation of the human embryonic stem cell line RCe007-A (RC-3). . 2016-05-00. Pubmed ID: 27346192; DOI: 10.1016/j.scr.2016.02.041 RCe007-A 2016-05-00 2016-05-00 PubMed: 27346192 DOI: 10.1016/j.scr.2016.02.041Associated cell lines:
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González-Pozas F, Montes R, López-Onieva L, Romero T, Domingo-Reinés J, Real PJ, Ramos-Mejía V, Ayllón V
Generation of human pluripotent stem cell lines with suppressed expression of the Notch ligand DLL4 using short hairpin RNAs
González-Pozas F et al. Generation of human pluripotent stem cell lines with suppressed expression of the Notch ligand DLL4 using short hairpin RNAs. . 2016-05-00. Pubmed ID: 27346199; DOI: 10.1016/j.scr.2016.04.005 GENYOi001-AGENYOi001-A-1GENYOi001-A-2WAe009-A-5WAe009-A-6 2016-05-00 2016-05-00 PubMed: 27346199 DOI: 10.1016/j.scr.2016.04.005Associated cell lines:
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De Sousa PA, Tye B, Bruce K, Dand P, Gardner J, Downie JM, Bateman M, Courtney A
Derivation of the human embryonic stem cell line RCe008-A (RC-4)
De Sousa PA et al. Derivation of the human embryonic stem cell line RCe008-A (RC-4). . 2016-05-00. Pubmed ID: 27346193; DOI: 10.1016/j.scr.2016.02.039 RCe008-A 2016-05-00 2016-05-00 PubMed: 27346193 DOI: 10.1016/j.scr.2016.02.039Associated cell lines:
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Hmadcha A, Aguilera Y, Lozano-Arana MD, Mellado N, Sánchez J, Moya C, Sánchez-Palazón L, Palacios J, Antiñolo G, Soria B
Derivation of HVR1, HVR2 and HVR3 human embryonic stem cell lines from IVF embryos after preimplantation genetic diagnosis (PGD) for monogenic disorder
Hmadcha A et al. Derivation of HVR1, HVR2 and HVR3 human embryonic stem cell lines from IVF embryos after preimplantation genetic diagnosis (PGD) for monogenic disorder. . 2016-05-00. Pubmed ID: 27346196; DOI: 10.1016/j.scr.2016.03.012 CABFPSe001-ACABFPSe002-ACABFPSe003-A 2016-05-00 2016-05-00 PubMed: 27346196 DOI: 10.1016/j.scr.2016.03.012Associated cell lines:
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Hansen SK, Borland H, Hasholt LF, Tümer Z, Nielsen JE, Rasmussen MA, Nielsen TT, Stummann TC, Fog K, Hyttel P
Generation of spinocerebellar ataxia type 3 patient-derived induced pluripotent stem cell line SCA3.B11
Hansen SK et al. Generation of spinocerebellar ataxia type 3 patient-derived induced pluripotent stem cell line SCA3.B11. . 2016-05-00. Pubmed ID: 27346191; DOI: 10.1016/j.scr.2016.02.042 BIONi010-B 2016-05-00 2016-05-00 PubMed: 27346191 DOI: 10.1016/j.scr.2016.02.042Associated cell lines:
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De Sousa PA, Tye BJ, Bruce K, Dand P, Russell G, Collins DM, Greenshields A, McDonald K, Bradburn H, Laurie A, Downie JM, Bateman M, Courtney A
Derivation of the clinical grade human embryonic stem cell line RCe016-A (RC-12)
De Sousa PA et al. Derivation of the clinical grade human embryonic stem cell line RCe016-A (RC-12). . 2016-05-00. Pubmed ID: 27346204; DOI: 10.1016/j.scr.2016.04.001 RCe016-A 2016-05-00 2016-05-00 PubMed: 27346204 DOI: 10.1016/j.scr.2016.04.001Associated cell lines:
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Greenwood-Goodwin M, Yang J, Hassanipour M, Larocca D
A novel lineage restricted, pericyte-like cell line isolated from human embryonic stem cells
Greenwood-Goodwin M et al. A novel lineage restricted, pericyte-like cell line isolated from human embryonic stem cells. . 2016-04-25. Pubmed ID: 27109637; DOI: 10.1038/srep24403; PMC: PMC4842973 SSCCe003-A 2016-04-25 2016-04-25 PubMed: 27109637 DOI: 10.1038/srep24403Associated cell lines:
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Rungsiwiwut R, Numchaisrika P, Ahnonkitpanit V, Virutamasen P, Pruksananonda K
Triploid human embryonic stem cells derived from tripronuclear zygotes displayed pluripotency and trophoblast differentiation ability similar to the diploid human embryonic stem cells
Rungsiwiwut R et al. Triploid human embryonic stem cells derived from tripronuclear zygotes displayed pluripotency and trophoblast differentiation ability similar to the diploid human embryonic stem cells. . 2016-04-22. Pubmed ID: 26821869; DOI: 10.1262/jrd.2015-113; PMC: PMC4848574 CHULAe001-A 2016-04-22 2016-04-22 PubMed: 26821869 DOI: 10.1262/jrd.2015-113Associated cell lines:
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Cao L, McDonnell A, Nitzsche A, Alexandrou A, Saintot PP, Loucif AJ, Brown AR, Young G, Mis M, Randall A, Waxman SG, Stanley P, Kirby S, Tarabar S, Gutteridge A, Butt R, McKernan RM, Whiting P, Ali Z, Bilsland J, Stevens EB
Pharmacological reversal of a pain phenotype in iPSC-derived sensory neurons and patients with inherited erythromelalgia
Cao L et al. Pharmacological reversal of a pain phenotype in iPSC-derived sensory neurons and patients with inherited erythromelalgia. . 2016-04-20. Pubmed ID: 27099175; DOI: 10.1126/scitranslmed.aad7653 RCi001-ARCi001-BRCi002-ARCi002-BPFIZi001-APFIZi002-APFIZi003-APFIZi004-A 2016-04-20 2016-04-20 PubMed: 27099175 DOI: 10.1126/scitranslmed.aad7653Associated cell lines:
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Guo G, von Meyenn F, Santos F, Chen Y, Reik W, Bertone P, Smith A, Nichols J
Naive Pluripotent Stem Cells Derived Directly from Isolated Cells of the Human Inner Cell Mass
Guo G et al. Naive Pluripotent Stem Cells Derived Directly from Isolated Cells of the Human Inner Cell Mass. . 2016-04-12. Pubmed ID: 26947977; DOI: 10.1016/j.stemcr.2016.02.005; PMC: PMC4834040 CAMe001-ACAMe002-A 2016-04-12 2016-04-12 PubMed: 26947977 DOI: 10.1016/j.stemcr.2016.02.005 -
Ichiyanagi N, Fujimori K, Yano M, Ishihara-Fujisaki C, Sone T, Akiyama T, Okada Y, Akamatsu W, Matsumoto T, Ishikawa M, Nishimoto Y, Ishihara Y, Sakuma T, Yamamoto T, Tsuiji H, Suzuki N, Warita H, Aoki M, Okano H
Establishment of In Vitro FUS-Associated Familial Amyotrophic Lateral Sclerosis Model Using Human Induced Pluripotent Stem Cells
Ichiyanagi N et al. Establishment of In Vitro FUS-Associated Familial Amyotrophic Lateral Sclerosis Model Using Human Induced Pluripotent Stem Cells. . 2016-04-12. Pubmed ID: 26997647; DOI: 10.1016/j.stemcr.2016.02.011; PMC: PMC4834049 CIRAi007-A 2016-04-12 2016-04-12 PubMed: 26997647 DOI: 10.1016/j.stemcr.2016.02.011Associated cell lines:
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Mandegar MA, Huebsch N, Frolov EB, Shin E, Truong A, Olvera MP, Chan AH, Miyaoka Y, Holmes K, Spencer CI, Judge LM, Gordon DE, Eskildsen TV, Villalta JE, Horlbeck MA, Gilbert LA, Krogan NJ, Sheikh SP, Weissman JS, Qi LS, So PL, Conklin BR
CRISPR Interference Efficiently Induces Specific and Reversible Gene Silencing in Human iPSCs
Mandegar MA et al. CRISPR Interference Efficiently Induces Specific and Reversible Gene Silencing in Human iPSCs. . 2016-04-07. Pubmed ID: 26971820; DOI: 10.1016/j.stem.2016.01.022; PMC: PMC4830697 UCSFi001-A 2016-04-07 2016-04-07 PubMed: 26971820 DOI: 10.1016/j.stem.2016.01.022Associated cell lines:
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Ito N, Hendriks WT, Dhakal J, Vaine CA, Liu C, Shin D, Shin K, Wakabayashi-Ito N, Dy M, Multhaupt-Buell T, Sharma N, Breakefield XO, Bragg DC
Decreased N-TAF1 expression in X-linked dystonia-parkinsonism patient-specific neural stem cells
Ito N et al. Decreased N-TAF1 expression in X-linked dystonia-parkinsonism patient-specific neural stem cells. . 2016-04-00. Pubmed ID: 26769797; DOI: 10.1242/dmm.022590; PMC: PMC4852502 XDPi001-AXDPi001-BXDPi002-AXDPi003-AXDPi004-AXDPi004-BXDPi005-AXDPi006-AXDPi006-BXDPi007-AXDPi007-BXDPi008-AXDPi008-BXDPi009-AXDPi010-AXDPi010-BXDPi011-AXDPi011-BXDPi012-AXDPi003-B 2016-04-00 2016-04-00 PubMed: 26769797 DOI: 10.1242/dmm.022590 -
Fernandes HJ, Hartfield EM, Christian HC, Emmanoulidou E, Zheng Y, Booth H, Bogetofte H, Lang C, Ryan BJ, Sardi SP, Badger J, Vowles J, Evetts S, Tofaris GK, Vekrellis K, Talbot K, Hu MT, James W, Cowley SA, Wade-Martins R
ER Stress and Autophagic Perturbations Lead to Elevated Extracellular α-Synuclein in GBA-N370S Parkinson's iPSC-Derived Dopamine Neurons
Fernandes HJ et al. ER Stress and Autophagic Perturbations Lead to Elevated Extracellular α-Synuclein in GBA-N370S Parkinson's iPSC-Derived Dopamine Neurons. . 2016-03-08. Pubmed ID: 26905200; DOI: 10.1016/j.stemcr.2016.01.013; PMC: PMC4788783 UOXFi001-AUOXFi001-BUOXFi003-AUOXFi004-BSTBCi025-ASTBCi025-BSTBCi026-ASTBCi026-B 2016-03-08 2016-03-08 PubMed: 26905200 DOI: 10.1016/j.stemcr.2016.01.013Associated cell lines:
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Handel AE, Chintawar S, Lalic T, Whiteley E, Vowles J, Giustacchini A, Argoud K, Sopp P, Nakanishi M, Bowden R, Cowley S, Newey S, Akerman C, Ponting CP, Cader MZ
Assessing similarity to primary tissue and cortical layer identity in induced pluripotent stem cell-derived cortical neurons through single-cell transcriptomics
Handel AE et al. Assessing similarity to primary tissue and cortical layer identity in induced pluripotent stem cell-derived cortical neurons through single-cell transcriptomics. . 2016-03-01. Pubmed ID: 26740550; DOI: 10.1093/hmg/ddv637; PMC: PMC4754051 STBCi321-A 2016-03-01 2016-03-01 PubMed: 26740550 DOI: 10.1093/hmg/ddv637Associated cell lines:
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Fatima A, Ivanyuk D, Herms S, Heilmann-Heimbach S, O'Shea O, Chapman C, Izsvák Z, Farr M, Hescheler J, Šarić T
Generation of human induced pluripotent stem cell line from a patient with a long QT syndrome type 2
Fatima A et al. Generation of human induced pluripotent stem cell line from a patient with a long QT syndrome type 2. . 2016-03-00. Pubmed ID: 27345990; DOI: 10.1016/j.scr.2015.12.039 UKKi009-AUKKi009-B 2016-03-00 2016-03-00 PubMed: 27345990 DOI: 10.1016/j.scr.2015.12.039 -
Rossbach B, Hildebrand L, El-Ahmad L, Stachelscheid H, Reinke P, Kurtz A
Generation of a human induced pluripotent stem cell line from urinary cells of a healthy donor using an integration free vector
Rossbach B et al. Generation of a human induced pluripotent stem cell line from urinary cells of a healthy donor using an integration free vector. . 2016-03-00. Pubmed ID: 27345993; DOI: 10.1016/j.scr.2015.12.018 WISCi004-ABCRTi004-A 2016-03-00 2016-03-00 PubMed: 27345993 DOI: 10.1016/j.scr.2015.12.018Associated cell lines:
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De Sousa PA, Tye BJ, Bruce K, Dand P, Russell G, Collins DM, Greenshields A, Bradburn H, Downie JM, Bateman M, Courtney A
Derivation of the human embryonic stem cell line RCe014-A (RC-10)
De Sousa PA et al. Derivation of the human embryonic stem cell line RCe014-A (RC-10). . 2016-03-00. Pubmed ID: 27346029; DOI: 10.1016/j.scr.2016.02.034 RCe014-A 2016-03-00 2016-03-00 PubMed: 27346029 DOI: 10.1016/j.scr.2016.02.034Associated cell lines:
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De Sousa PA, Tye BJ, Sneddon S, Bruce K, Dand P, Russell G, Collins DM, Greenshields A, McDonald K, Bradburn H, Gardner J, Downie JM, Courtney A, Brison DR
Derivation of the human embryonic stem cell line RCM1
De Sousa PA et al. Derivation of the human embryonic stem cell line RCM1. . 2016-03-00. Pubmed ID: 27346018; DOI: 10.1016/j.scr.2015.12.020 RCe005-A 2016-03-00 2016-03-00 PubMed: 27346018 DOI: 10.1016/j.scr.2015.12.020Associated cell lines:
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Dumevska B, Bosman A, McKernan R, Schmidt U, Peura T
Derivation of human embryonic stem cell line Genea022
Dumevska B et al. Derivation of human embryonic stem cell line Genea022. . 2016-03-00. Pubmed ID: 27346017; DOI: 10.1016/j.scr.2016.02.011 GENEAe016-A 2016-03-00 2016-03-00 PubMed: 27346017 DOI: 10.1016/j.scr.2016.02.011Associated cell lines:
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Jacquet L, Hewitson H, Wood V, Kadeva N, Cornwell G, Codognotto S, Stephenson E, Ilic D
Generation of KCL013 research grade human embryonic stem cell line carrying a mutation in the HTT gene
Jacquet L et al. Generation of KCL013 research grade human embryonic stem cell line carrying a mutation in the HTT gene. . 2016-03-00. Pubmed ID: 27345987; DOI: 10.1016/j.scr.2016.01.011; PMC: PMC4823765 KCLe010-A 2016-03-00 2016-03-00 PubMed: 27345987 DOI: 10.1016/j.scr.2016.01.011Associated cell lines:
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Dumevska B, Peura T, McKernan R, Goel D, Schmidt U
Derivation of Huntington disease affected Genea020 human embryonic stem cell line
Dumevska B et al. Derivation of Huntington disease affected Genea020 human embryonic stem cell line. . 2016-03-00. Pubmed ID: 27346007; DOI: 10.1016/j.scr.2016.02.009 GENEAe015-A 2016-03-00 2016-03-00 PubMed: 27346007 DOI: 10.1016/j.scr.2016.02.009Associated cell lines:
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De Sousa PA, Tye BJ, Bruce K, Dand P, Russell G, Collins DM, Bradburn H, Gardner J, Downie JM, Bateman M, Courtney A
Derivation of the human embryonic stem cell line RCe010-A (RC-6)
De Sousa PA et al. Derivation of the human embryonic stem cell line RCe010-A (RC-6). . 2016-03-00. Pubmed ID: 27346019; DOI: 10.1016/j.scr.2016.02.035 RCe010-A 2016-03-00 2016-03-00 PubMed: 27346019 DOI: 10.1016/j.scr.2016.02.035Associated cell lines:
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Hewitson H, Wood V, Kadeva N, Cornwell G, Codognotto S, Stephenson E, Ilic D
Generation of KCL017 research grade human embryonic stem cell line carrying a mutation in VHL gene
Hewitson H et al. Generation of KCL017 research grade human embryonic stem cell line carrying a mutation in VHL gene. . 2016-03-00. Pubmed ID: 27345980; DOI: 10.1016/j.scr.2016.01.013; PMC: PMC4823763 KCLe013-A 2016-03-00 2016-03-00 PubMed: 27345980 DOI: 10.1016/j.scr.2016.01.013Associated cell lines:
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Jacquet L, Hewitson H, Wood V, Kadeva N, Cornwell G, Codognotto S, Hobbs C, Stephenson E, Ilic D
Generation of KCL012 research grade human embryonic stem cell line carrying a mutation in the HTT gene
Jacquet L et al. Generation of KCL012 research grade human embryonic stem cell line carrying a mutation in the HTT gene. . 2016-03-00. Pubmed ID: 27345979; DOI: 10.1016/j.scr.2016.01.012; PMC: PMC4823764 KCLe009-A 2016-03-00 2016-03-00 PubMed: 27345979 DOI: 10.1016/j.scr.2016.01.012Associated cell lines:
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Dumevska B, McKernan R, Hu J, Schmidt U
Derivation of Huntington Disease affected Genea089 human embryonic stem cell line
Dumevska B et al. Derivation of Huntington Disease affected Genea089 human embryonic stem cell line. . 2016-03-00. Pubmed ID: 27346008; DOI: 10.1016/j.scr.2016.02.013 GENEAe013-A 2016-03-00 2016-03-00 PubMed: 27346008 DOI: 10.1016/j.scr.2016.02.013Associated cell lines:
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Dumevska B, Bosman A, McKernan R, Main H, Schmidt U, Peura T
Derivation of Trisomy 21 affected human embryonic stem cell line Genea021
Dumevska B et al. Derivation of Trisomy 21 affected human embryonic stem cell line Genea021. . 2016-03-00. Pubmed ID: 27346003; DOI: 10.1016/j.scr.2016.02.010 GENEAe021-A 2016-03-00 2016-03-00 PubMed: 27346003 DOI: 10.1016/j.scr.2016.02.010Associated cell lines:
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Questa M, Romorini L, Blüguermann C, Solari CM, Neiman G, Luzzani C, Scassa MÉ, Sevlever GE, Guberman AS, Miriuka SG
Generation of iPSC line iPSC-FH2.1 in hypoxic conditions from human foreskin fibroblasts
Questa M et al. Generation of iPSC line iPSC-FH2.1 in hypoxic conditions from human foreskin fibroblasts. . 2016-03-00. Pubmed ID: 27345989; DOI: 10.1016/j.scr.2015.12.026 INEUi002-A 2016-03-00 2016-03-00 PubMed: 27345989 DOI: 10.1016/j.scr.2015.12.026Associated cell lines:
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Dumevska B, Schaft J, McKernan R, Hu J, Schmidt U
Derivation of Huntington Disease affected Genea090 human embryonic stem cell line
Dumevska B et al. Derivation of Huntington Disease affected Genea090 human embryonic stem cell line. . 2016-03-00. Pubmed ID: 27346026; DOI: 10.1016/j.scr.2016.02.024 GENEAe018-A 2016-03-00 2016-03-00 PubMed: 27346026 DOI: 10.1016/j.scr.2016.02.024Associated cell lines:
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Dumevska B, Peura T, McKernan R, Goel D, Schmidt U
Derivation of human embryonic stem cell line Genea019
Dumevska B et al. Derivation of human embryonic stem cell line Genea019. . 2016-03-00. Pubmed ID: 27346002; DOI: 10.1016/j.scr.2016.02.008 GENEAe020-A 2016-03-00 2016-03-00 PubMed: 27346002 DOI: 10.1016/j.scr.2016.02.008Associated cell lines:
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Dumevska B, Bosman A, McKernan R, Goel D, Schmidt U, Peura T
Derivation of human embryonic stem cell line Genea023
Dumevska B et al. Derivation of human embryonic stem cell line Genea023. . 2016-03-00. Pubmed ID: 27346015; DOI: 10.1016/j.scr.2016.02.012 GENEAe017-A 2016-03-00 2016-03-00 PubMed: 27346015 DOI: 10.1016/j.scr.2016.02.012Associated cell lines:
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De Sousa PA, Tye B, Bruce K, Dand P, Russell G, Collins DM, Gardner J, Downie JM, Bateman M, Courtney A
Derivation of the human embryonic stem cell line RCe009-A (RC-5)
De Sousa PA et al. Derivation of the human embryonic stem cell line RCe009-A (RC-5). . 2016-03-00. Pubmed ID: 27346004; DOI: 10.1016/j.scr.2016.02.030 RCe007-ARCe009-A 2016-03-00 2016-03-00 PubMed: 27346004 DOI: 10.1016/j.scr.2016.02.030 -
De Sousa PA, Tye BJ, Collins DM, Bruce K, Dand P, Russell G, Bradburn H, Downie JM, Bateman M, Courtney A
Derivation of the human embryonic stem cell line RCe011-A (RC-7)
De Sousa PA et al. Derivation of the human embryonic stem cell line RCe011-A (RC-7). . 2016-03-00. Pubmed ID: 27346020; DOI: 10.1016/j.scr.2016.02.036 RCe011-A 2016-03-00 2016-03-00 PubMed: 27346020 DOI: 10.1016/j.scr.2016.02.036Associated cell lines:
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Dumevska B, Schaft J, McKernan R, Hu J, Schmidt U
Derivation of Huntington Disease affected Genea091 human embryonic stem cell line
Dumevska B et al. Derivation of Huntington Disease affected Genea091 human embryonic stem cell line. . 2016-03-00. Pubmed ID: 27346013; DOI: 10.1016/j.scr.2016.02.022 GENEAe019-A 2016-03-00 2016-03-00 PubMed: 27346013 DOI: 10.1016/j.scr.2016.02.022Associated cell lines:
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De Sousa PA, Tye B, Bruce K, Dand P, Russell G, Gardner J, Downie JM, Bateman M, Courtney A
Derivation of the human embryonic stem cell line RCe006-A (RC-2)
De Sousa PA et al. Derivation of the human embryonic stem cell line RCe006-A (RC-2). . 2016-03-00. Pubmed ID: 27346014; DOI: 10.1016/j.scr.2016.02.029 RCe006-A 2016-03-00 2016-03-00 PubMed: 27346014 DOI: 10.1016/j.scr.2016.02.029Associated cell lines:
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Miere C, Hewitson H, Devito L, Wood V, Kadeva N, Cornwell G, Codognotto S, Stephenson E, Ilic D
Generation of KCL018 research grade human embryonic stem cell line carrying a mutation in the DMPK gene
Miere C et al. Generation of KCL018 research grade human embryonic stem cell line carrying a mutation in the DMPK gene. . 2016-03-00. Pubmed ID: 27346000; DOI: 10.1016/j.scr.2016.01.004; PMC: PMC4823665 KCLe014-A 2016-03-00 2016-03-00 PubMed: 27346000 DOI: 10.1016/j.scr.2016.01.004Associated cell lines:
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De Sousa PA, Tye BJ, Bruce K, Dand P, Russell G, Collins DM, Greenshields A, Bradburn H, Downie JM, Bateman M, Courtney A
Derivation of the human embryonic stem cell line RCe012-A (RC-8)
De Sousa PA et al. Derivation of the human embryonic stem cell line RCe012-A (RC-8). . 2016-03-00. Pubmed ID: 27346021; DOI: 10.1016/j.scr.2016.02.033 RCe012-A 2016-03-00 2016-03-00 PubMed: 27346021 DOI: 10.1016/j.scr.2016.02.033Associated cell lines:
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Asplund A, Pradip A, van Giezen M, Aspegren A, Choukair H, Rehnström M, Jacobsson S, Ghosheh N, El Hajjam D, Holmgren S, Larsson S, Benecke J, Butron M, Wigander A, Noaksson K, Sartipy P, Björquist P, Edsbagge J, Küppers-Munther B
One Standardized Differentiation Procedure Robustly Generates Homogenous Hepatocyte Cultures Displaying Metabolic Diversity from a Large Panel of Human Pluripotent Stem Cells
Asplund A et al. One Standardized Differentiation Procedure Robustly Generates Homogenous Hepatocyte Cultures Displaying Metabolic Diversity from a Large Panel of Human Pluripotent Stem Cells. . 2016-02-00. Pubmed ID: 26385115; DOI: 10.1007/s12015-015-9621-9 CEBe012-ACEBe014-ACEBe015-ACEBe027-AESe019-AUODi001-ACEBi001-A 2016-02-00 2016-02-00 PubMed: 26385115 DOI: 10.1007/s12015-015-9621-9 -
Desmarais JA, Unger C, Damjanov I, Meuth M, Andrews P
Apoptosis and failure of checkpoint kinase 1 activation in human induced pluripotent stem cells under replication stress
Desmarais JA et al. Apoptosis and failure of checkpoint kinase 1 activation in human induced pluripotent stem cells under replication stress. . 2016-01-25. Pubmed ID: 26810087; DOI: 10.1186/s13287-016-0279-2; PMC: PMC4727355 UOSi001-AUOSi001-B 2016-01-25 2016-01-25 PubMed: 26810087 DOI: 10.1186/s13287-016-0279-2 -
Seltmann S, Lekschas F, Müller R, Stachelscheid H, Bittner MS, Zhang W, Kidane L, Seriola A, Veiga A, Stacey G, Kurtz A
hPSCreg--the human pluripotent stem cell registry
Seltmann S et al. hPSCreg--the human pluripotent stem cell registry. . 2016-01-04. Pubmed ID: 26400179; DOI: 10.1093/nar/gkv963; PMC: PMC4702942 WAe009-A 2016-01-04 2016-01-04 PubMed: 26400179 DOI: 10.1093/nar/gkv963Associated cell lines:
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Rasmussen MA, Hjermind LE, Hasholt LF, Waldemar G, Nielsen JE, Clausen C, Hyttel P, Holst B
Induced pluripotent stem cells (iPSCs) derived from a patient with frontotemporal dementia caused by a P301L mutation in microtubule-associated protein tau (MAPT)
Rasmussen MA et al. Induced pluripotent stem cells (iPSCs) derived from a patient with frontotemporal dementia caused by a P301L mutation in microtubule-associated protein tau (MAPT). . 2016-01-00. Pubmed ID: 27345788; DOI: 10.1016/j.scr.2015.12.008 BIONi010-A 2016-01-00 2016-01-00 PubMed: 27345788 DOI: 10.1016/j.scr.2015.12.008Associated cell lines:
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Rasmussen MA, Hjermind LE, Hasholt LF, Waldemar G, Nielsen JE, Clausen C, Hyttel P, Holst B
Induced pluripotent stem cells (iPSCs) derived from a patient with frontotemporal dementia caused by a R406W mutation in microtubule-associated protein tau (MAPT)
Rasmussen MA et al. Induced pluripotent stem cells (iPSCs) derived from a patient with frontotemporal dementia caused by a R406W mutation in microtubule-associated protein tau (MAPT). . 2016-01-00. Pubmed ID: 27345789; DOI: 10.1016/j.scr.2015.12.006 BIONi010-A 2016-01-00 2016-01-00 PubMed: 27345789 DOI: 10.1016/j.scr.2015.12.006Associated cell lines:
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Rasmussen MA, Hjermind LE, Hasholt LF, Waldemar G, Nielsen JE, Clausen C, Hyttel P, Holst B
Induced pluripotent stem cells (iPSCs) derived from a pre-symptomatic carrier of a R406W mutation in microtubule-associated protein tau (MAPT) causing frontotemporal dementia
Rasmussen MA et al. Induced pluripotent stem cells (iPSCs) derived from a pre-symptomatic carrier of a R406W mutation in microtubule-associated protein tau (MAPT) causing frontotemporal dementia. . 2016-01-00. Pubmed ID: 27345791; DOI: 10.1016/j.scr.2015.12.012 BIONi010-A 2016-01-00 2016-01-00 PubMed: 27345791 DOI: 10.1016/j.scr.2015.12.012Associated cell lines:
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Rossbach B, Hildebrand L, El-Ahmad L, Stachelscheid H, Reinke P, Kurtz A
WITHDRAWN: Generation of a human induced pluripotent stem cell line from urinary cells of a healthy donor using integration free Sendai technology
Rossbach B et al. WITHDRAWN: Generation of a human induced pluripotent stem cell line from urinary cells of a healthy donor using integration free Sendai technology. . 2016-01-00. Pubmed ID: 27345798; DOI: 10.1016/j.scr.2015.12.021 WISCi004-ABCRTi004-A 2016-01-00 2016-01-00 PubMed: 27345798 DOI: 10.1016/j.scr.2015.12.021Associated cell lines:
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Tubsuwan A, Pires C, Rasmussen MA, Schmid B, Nielsen JE, Hjermind LE, Hall V, Nielsen TT, Waldemar G, Hyttel P, Clausen C, Kitiyanant N, Freude KK, Holst B
Generation of induced pluripotent stem cells (iPSCs) from an Alzheimer's disease patient carrying a L150P mutation in PSEN-1
Tubsuwan A et al. Generation of induced pluripotent stem cells (iPSCs) from an Alzheimer's disease patient carrying a L150P mutation in PSEN-1. . 2016-01-00. Pubmed ID: 27345792; DOI: 10.1016/j.scr.2015.12.015 BIONi010-A 2016-01-00 2016-01-00 PubMed: 27345792 DOI: 10.1016/j.scr.2015.12.015Associated cell lines:
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Miere C, Hewitson H, Wood V, Kadeva N, Cornwell G, Codognotto S, Stephenson E, Ilic D
Generation of KCL016 research grade human embryonic stem cell line carrying a mutation in VHL gene
Miere C et al. Generation of KCL016 research grade human embryonic stem cell line carrying a mutation in VHL gene. . 2016-01-00. Pubmed ID: 27345783; DOI: 10.1016/j.scr.2015.12.003; PMC: PMC4757726 KCLe012-A 2016-01-00 2016-01-00 PubMed: 27345783 DOI: 10.1016/j.scr.2015.12.003Associated cell lines:
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Hildebrand L, Rossbach B, Kühnen P, Gossen M, Kurtz A, Reinke P, Seemann P, Stachelscheid H
Generation of integration free induced pluripotent stem cells from fibrodysplasia ossificans progressiva (FOP) patients from urine samples
Hildebrand L et al. Generation of integration free induced pluripotent stem cells from fibrodysplasia ossificans progressiva (FOP) patients from urine samples. . 2016-01-00. Pubmed ID: 27345784; DOI: 10.1016/j.scr.2015.11.017 BCRTi001-ABCRTi002-A 2016-01-00 2016-01-00 PubMed: 27345784 DOI: 10.1016/j.scr.2015.11.017Associated cell lines:
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Si-Tayeb K, Idriss S, Champon B, Caillaud A, Pichelin M, Arnaud L, Lemarchand P, Le May C, Zibara K, Cariou B
Urine-sample-derived human induced pluripotent stem cells as a model to study PCSK9-mediated autosomal dominant hypercholesterolemia
Si-Tayeb K et al. Urine-sample-derived human induced pluripotent stem cells as a model to study PCSK9-mediated autosomal dominant hypercholesterolemia. . 2016-01-00. Pubmed ID: 26586530; DOI: 10.1242/dmm.022277; PMC: PMC4728336 ITXi001-A 2016-01-00 2016-01-00 PubMed: 26586530 DOI: 10.1242/dmm.022277Associated cell lines:
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Kang H, Minder P, Park MA, Mesquitta WT, Torbett BE, Slukvin II
CCR5 Disruption in Induced Pluripotent Stem Cells Using CRISPR/Cas9 Provides Selective Resistance of Immune Cells to CCR5-tropic HIV-1 Virus
Kang H et al. CCR5 Disruption in Induced Pluripotent Stem Cells Using CRISPR/Cas9 Provides Selective Resistance of Immune Cells to CCR5-tropic HIV-1 Virus. . 2015-12-15. Pubmed ID: 26670276; DOI: 10.1038/mtna.2015.42 WAi001-A-1WAi001-B 2015-12-15 2015-12-15 PubMed: 26670276 DOI: 10.1038/mtna.2015.42Associated cell lines:
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Schwab AJ, Ebert AD
Neurite Aggregation and Calcium Dysfunction in iPSC-Derived Sensory Neurons with Parkinson's Disease-Related LRRK2 G2019S Mutation
Schwab AJ et al. Neurite Aggregation and Calcium Dysfunction in iPSC-Derived Sensory Neurons with Parkinson's Disease-Related LRRK2 G2019S Mutation. . 2015-12-08. Pubmed ID: 26651604; DOI: 10.1016/j.stemcr.2015.11.004; PMC: PMC4682343 MUSCSDi001-A 2015-12-08 2015-12-08 PubMed: 26651604 DOI: 10.1016/j.stemcr.2015.11.004Associated cell lines:
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Chung YG, Matoba S, Liu Y, Eum JH, Lu F, Jiang W, Lee JE, Sepilian V, Cha KY, Lee DR, Zhang Y
Histone Demethylase Expression Enhances Human Somatic Cell Nuclear Transfer Efficiency and Promotes Derivation of Pluripotent Stem Cells
Chung YG et al. Histone Demethylase Expression Enhances Human Somatic Cell Nuclear Transfer Efficiency and Promotes Derivation of Pluripotent Stem Cells. . 2015-12-03. Pubmed ID: 26526725; DOI: 10.1016/j.stem.2015.10.001 CHAHESe001-A 2015-12-03 2015-12-03 PubMed: 26526725 DOI: 10.1016/j.stem.2015.10.001Associated cell lines:
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Shimojo D, Onodera K, Doi-Torii Y, Ishihara Y, Hattori C, Miwa Y, Tanaka S, Okada R, Ohyama M, Shoji M, Nakanishi A, Doyu M, Okano H, Okada Y
Rapid, efficient, and simple motor neuron differentiation from human pluripotent stem cells
Shimojo D et al. Rapid, efficient, and simple motor neuron differentiation from human pluripotent stem cells. . 2015-12-01. Pubmed ID: 26626025; DOI: 10.1186/s13041-015-0172-4; PMC: PMC4666063 KUIFMSi004-C 2015-12-01 2015-12-01 PubMed: 26626025 DOI: 10.1186/s13041-015-0172-4Associated cell lines:
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Kuusela J, Kujala VJ, Kiviaho A, Ojala M, Swan H, Kontula K, Aalto-Setälä K
Effects of cardioactive drugs on human induced pluripotent stem cell derived long QT syndrome cardiomyocytes
Kuusela J et al. Effects of cardioactive drugs on human induced pluripotent stem cell derived long QT syndrome cardiomyocytes. . 2016-00-00. Pubmed ID: 27026928; DOI: 10.1186/s40064-016-1889-y; PMC: PMC4771667 TAUi007-ATAUi007-B 2016-00-00 2016-00-00 PubMed: 27026928 DOI: 10.1186/s40064-016-1889-y -
Holmqvist S, Lehtonen Š, Chumarina M, Puttonen KA, Azevedo C, Lebedeva O, Ruponen M, Oksanen M, Djelloul M, Collin A, Goldwurm S, Meyer M, Lagarkova M, Kiselev S, Koistinaho J, Roybon L
Creation of a library of induced pluripotent stem cells from Parkinsonian patients
Holmqvist S et al. Creation of a library of induced pluripotent stem cells from Parkinsonian patients. . 2016-00-00. Pubmed ID: 28725696; DOI: 10.1038/npjparkd.2016.9; PMC: PMC5516589 RCPCMi009-A 2016-00-00 2016-00-00 PubMed: 28725696 DOI: 10.1038/npjparkd.2016.9Associated cell lines:
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Nagaria PK, Robert C, Park TS, Huo JS, Zambidis ET, Rassool FV
High-Fidelity Reprogrammed Human IPSCs Have a High Efficacy of DNA Repair and Resemble hESCs in Their MYC Transcriptional Signature
Nagaria PK et al. High-Fidelity Reprogrammed Human IPSCs Have a High Efficacy of DNA Repair and Resemble hESCs in Their MYC Transcriptional Signature. . 2016-00-00. Pubmed ID: 27688775; DOI: 10.1155/2016/3826249; PMC: PMC5023833 WAe007-AWAe009-AESIBIe003-ATMOi001-A 2016-00-00 2016-00-00 PubMed: 27688775 DOI: 10.1155/2016/3826249Associated cell lines:
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Hossini AM, Quast AS, Plötz M, Grauel K, Exner T, Küchler J, Stachelscheid H, Eberle J, Rabien A, Makrantonaki E, Zouboulis CC
PI3K/AKT Signaling Pathway Is Essential for Survival of Induced Pluripotent Stem Cells
Hossini AM et al. PI3K/AKT Signaling Pathway Is Essential for Survival of Induced Pluripotent Stem Cells. . 2016-00-00. Pubmed ID: 27138223; DOI: 10.1371/journal.pone.0154770; PMC: PMC4854383 WAe001-ABIHi001-ABIHi004-A 2016-00-00 2016-00-00 PubMed: 27138223 DOI: 10.1371/journal.pone.0154770 -
Féraud O, Valogne Y, Melkus MW, Zhang Y, Oudrhiri N, Haddad R, Daury A, Rocher C, Larbi A, Duquesnoy P, Divers D, Gobbo E, Brunet de la Grange P, Louache F, Bennaceur-Griscelli A, Mitjavila-Garcia MT
Donor Dependent Variations in Hematopoietic Differentiation among Embryonic and Induced Pluripotent Stem Cell Lines
Féraud O et al. Donor Dependent Variations in Hematopoietic Differentiation among Embryonic and Induced Pluripotent Stem Cell Lines. . 2016-00-00. Pubmed ID: 26938212; DOI: 10.1371/journal.pone.0149291; PMC: PMC4777368 UPSFRi001-AUPSFRi002-AUPSFRi004-AUPSFRi006-AUPSFRi007-AUPSFRi008-AUPSFRi009-A 2016-00-00 2016-00-00 PubMed: 26938212 DOI: 10.1371/journal.pone.0149291Associated cell lines:
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Momcilovic O, Sivapatham R, Oron TR, Meyer M, Mooney S, Rao MS, Zeng X
Derivation, Characterization, and Neural Differentiation of Integration-Free Induced Pluripotent Stem Cell Lines from Parkinson's Disease Patients Carrying SNCA, LRRK2, PARK2, and GBA Mutations
Momcilovic O et al. Derivation, Characterization, and Neural Differentiation of Integration-Free Induced Pluripotent Stem Cell Lines from Parkinson's Disease Patients Carrying SNCA, LRRK2, PARK2, and GBA Mutations. . 2016-00-00. Pubmed ID: 27191603; DOI: 10.1371/journal.pone.0154890; PMC: PMC4871453 CRMi003-A-1 2016-00-00 2016-00-00 PubMed: 27191603 DOI: 10.1371/journal.pone.0154890Associated cell lines:
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Ojala M, Prajapati C, Pölönen RP, Rajala K, Pekkanen-Mattila M, Rasku J, Larsson K, Aalto-Setälä K
Mutation-Specific Phenotypes in hiPSC-Derived Cardiomyocytes Carrying Either Myosin-Binding Protein C Or α-Tropomyosin Mutation for Hypertrophic Cardiomyopathy
Ojala M et al. Mutation-Specific Phenotypes in hiPSC-Derived Cardiomyocytes Carrying Either Myosin-Binding Protein C Or α-Tropomyosin Mutation for Hypertrophic Cardiomyopathy. . 2016-00-00. Pubmed ID: 27057166; DOI: 10.1155/2016/1684792; PMC: PMC4707351 TAUi002-A 2016-00-00 2016-00-00 PubMed: 27057166 DOI: 10.1155/2016/1684792Associated cell lines:
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Riera M, Fontrodona L, Albert S, Ramirez DM, Seriola A, Salas A, Muñoz Y, Ramos D, Villegas-Perez MP, Zapata MA, Raya A, Ruberte J, Veiga A, Garcia-Arumi J
Comparative study of human embryonic stem cells (hESC) and human induced pluripotent stem cells (hiPSC) as a treatment for retinal dystrophies
Riera M et al. Comparative study of human embryonic stem cells (hESC) and human induced pluripotent stem cells (hiPSC) as a treatment for retinal dystrophies. . 2016-00-00. Pubmed ID: 27006969; DOI: 10.1038/mtm.2016.10; PMC: PMC4793806 ESe014-A 2016-00-00 2016-00-00 PubMed: 27006969 DOI: 10.1038/mtm.2016.10Associated cell lines:
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Canham MA, Van Deusen A, Brison DR, De Sousa PA, Downie J, Devito L, Hewitt ZA, Ilic D, Kimber SJ, Moore HD, Murray H, Kunath T
The Molecular Karyotype of 25 Clinical-Grade Human Embryonic Stem Cell Lines
Canham MA et al. The Molecular Karyotype of 25 Clinical-Grade Human Embryonic Stem Cell Lines. . 2015-11-26. Pubmed ID: 26607962; DOI: 10.1038/srep17258; PMC: PMC4660465 RCe013-ARCe015-ARCe021-AUMANe003-ACMFTe002-AUOSe007-AUOSe008-AUOSe009-AUOSe010-AUOSe012-AUOSe013-AUOSe014-AUOSe015-AUOSe016-AUOSe017-AUOSe018-A 2015-11-26 2015-11-26 PubMed: 26607962 DOI: 10.1038/srep17258 -
Oliveira LM, Falomir-Lockhart LJ, Botelho MG, Lin KH, Wales P, Koch JC, Gerhardt E, Taschenberger H, Outeiro TF, Lingor P, Schüle B, Arndt-Jovin DJ, Jovin TM
Elevated α-synuclein caused by SNCA gene triplication impairs neuronal differentiation and maturation in Parkinson's patient-derived induced pluripotent stem cells
Oliveira LM et al. Elevated α-synuclein caused by SNCA gene triplication impairs neuronal differentiation and maturation in Parkinson's patient-derived induced pluripotent stem cells. . 2015-11-26. Pubmed ID: 26610207; DOI: 10.1038/cddis.2015.318; PMC: PMC4670926 SUSMi005-A 2015-11-26 2015-11-26 PubMed: 26610207 DOI: 10.1038/cddis.2015.318Associated cell lines:
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Ng SY, Soh BS, Rodriguez-Muela N, Hendrickson DG, Price F, Rinn JL, Rubin LL
Genome-wide RNA-Seq of Human Motor Neurons Implicates Selective ER Stress Activation in Spinal Muscular Atrophy
Ng SY et al. Genome-wide RNA-Seq of Human Motor Neurons Implicates Selective ER Stress Activation in Spinal Muscular Atrophy. . 2015-11-05. Pubmed ID: 26321202; DOI: 10.1016/j.stem.2015.08.003; PMC: PMC4839185 HVRDi016-AHVRDi017-A 2015-11-05 2015-11-05 PubMed: 26321202 DOI: 10.1016/j.stem.2015.08.003Associated cell lines:
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Montes R, Romero T, Cabrera S, Ayllon V, Lopez-Escamez JA, Ramos-Mejia V, Real PJ
Generation and characterization of the human iPSC line PBMC1-iPS4F1 from adult peripheral blood mononuclear cells
Montes R et al. Generation and characterization of the human iPSC line PBMC1-iPS4F1 from adult peripheral blood mononuclear cells. . 2015-11-00. Pubmed ID: 26987924; DOI: 10.1016/j.scr.2015.10.009 GENYOi001-A 2015-11-00 2015-11-00 PubMed: 26987924 DOI: 10.1016/j.scr.2015.10.009Associated cell lines:
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Tangprasittipap A, Satirapod C, Jittorntrum B, Lertritanan S, Anurathaphan U, Phanthong P, Borwornpinyo S, Kitiyanant N, Hongeng S
Generation of iPSC line MU011.A-hiPS from homozygous α-thalassemia fetal skin fibroblasts
Tangprasittipap A et al. Generation of iPSC line MU011.A-hiPS from homozygous α-thalassemia fetal skin fibroblasts. . 2015-11-00. Pubmed ID: 26432158; DOI: 10.1016/j.scr.2015.09.003 MUi011-A 2015-11-00 2015-11-00 PubMed: 26432158 DOI: 10.1016/j.scr.2015.09.003Associated cell lines:
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Birket MJ, Ribeiro MC, Kosmidis G, Ward D, Leitoguinho AR, van de Pol V, Dambrot C, Devalla HD, Davis RP, Mastroberardino PG, Atsma DE, Passier R, Mummery CL
Contractile Defect Caused by Mutation in MYBPC3 Revealed under Conditions Optimized for Human PSC-Cardiomyocyte Function
Birket MJ et al. Contractile Defect Caused by Mutation in MYBPC3 Revealed under Conditions Optimized for Human PSC-Cardiomyocyte Function. . 2015-10-27. Pubmed ID: 26489474; DOI: 10.1016/j.celrep.2015.09.025; PMC: PMC4644234 LUMCi029-B 2015-10-27 2015-10-27 PubMed: 26489474 DOI: 10.1016/j.celrep.2015.09.025Associated cell lines:
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Mariappan I, Maddileti S, Joseph P, Siamwala JH, Vauhini V
Enriched Cultures of Retinal Cells From BJNhem20 Human Embryonic Stem Cell Line of Indian Origin
Mariappan I et al. Enriched Cultures of Retinal Cells From BJNhem20 Human Embryonic Stem Cell Line of Indian Origin. . 2015-10-00. Pubmed ID: 26567782; DOI: 10.1167/iovs.15-17364 JNCSRe002-A 2015-10-00 2015-10-00 PubMed: 26567782 DOI: 10.1167/iovs.15-17364Associated cell lines:
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Sposito T, Preza E, Mahoney CJ, Setó-Salvia N, Ryan NS, Morris HR, Arber C, Devine MJ, Houlden H, Warner TT, Bushell TJ, Zagnoni M, Kunath T, Livesey FJ, Fox NC, Rossor MN, Hardy J, Wray S
Developmental regulation of tau splicing is disrupted in stem cell-derived neurons from frontotemporal dementia patients with the 10 + 16 splice-site mutation in MAPT
Sposito T et al. Developmental regulation of tau splicing is disrupted in stem cell-derived neurons from frontotemporal dementia patients with the 10 + 16 splice-site mutation in MAPT. . 2015-09-15. Pubmed ID: 26136155; DOI: 10.1093/hmg/ddv246; PMC: PMC4550814 UCLi003-AUCLi003-B 2015-09-15 2015-09-15 PubMed: 26136155 DOI: 10.1093/hmg/ddv246 -
Kiviaho AL, Ahola A, Larsson K, Penttinen K, Swan H, Pekkanen-Mattila M, Venäläinen H, Paavola K, Hyttinen J, Aalto-Setälä K
Distinct electrophysiological and mechanical beating phenotypes of long QT syndrome type 1-specific cardiomyocytes carrying different mutations
Kiviaho AL et al. Distinct electrophysiological and mechanical beating phenotypes of long QT syndrome type 1-specific cardiomyocytes carrying different mutations. . 2015-09-01. Pubmed ID: 28785673; DOI: 10.1016/j.ijcha.2015.04.008; PMC: PMC5497295 TAUi002-ATAUi006-ATAUi006-BTAUi007-ATAUi007-B 2015-09-01 2015-09-01 PubMed: 28785673 DOI: 10.1016/j.ijcha.2015.04.008 -
Srikanth P, Han K, Callahan DG, Makovkina E, Muratore CR, Lalli MA, Zhou H, Boyd JD, Kosik KS, Selkoe DJ, Young-Pearse TL
Genomic DISC1 Disruption in hiPSCs Alters Wnt Signaling and Neural Cell Fate
Srikanth P et al. Genomic DISC1 Disruption in hiPSCs Alters Wnt Signaling and Neural Cell Fate. . 2015-09-01. Pubmed ID: 26299970; DOI: 10.1016/j.celrep.2015.07.061; PMC: PMC4558300 WISCi004-A-1WISCi004-A-2WISCi004-A-3WISCi004-A-4 2015-09-01 2015-09-01 PubMed: 26299970 DOI: 10.1016/j.celrep.2015.07.061Associated cell lines:
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Ávila-González D, Vega-Hernández E, Regalado-Hernández JC, De la Jara-Díaz JF, García-Castro IL, Molina-Hernández A, Moreno-Verduzco ER, Razo-Aguilera G, Flores-Herrera H, Portillo W, Díaz-Martínez NE, García-López G, Díaz NF
Human amniotic epithelial cells as feeder layer to derive and maintain human embryonic stem cells from poor-quality embryos
Ávila-González D et al. Human amniotic epithelial cells as feeder layer to derive and maintain human embryonic stem cells from poor-quality embryos. . 2015-09-00. Pubmed ID: 26246271; DOI: 10.1016/j.scr.2015.07.006 INPERe001-A 2015-09-00 2015-09-00 PubMed: 26246271 DOI: 10.1016/j.scr.2015.07.006Associated cell lines:
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Cabrera S, Ji AR, Frejo L, Ramos-Mejia V, Romero T, Real P, Lopez-Escamez JA
Generation of human iPSC line GRX-MCiPS4F-A2 from adult peripheral blood mononuclear cells (PBMCs) with Spanish genetic background
Cabrera S et al. Generation of human iPSC line GRX-MCiPS4F-A2 from adult peripheral blood mononuclear cells (PBMCs) with Spanish genetic background. . 2015-09-00. Pubmed ID: 26284980; DOI: 10.1016/j.scr.2015.07.002 GENYOi006-A 2015-09-00 2015-09-00 PubMed: 26284980 DOI: 10.1016/j.scr.2015.07.002Associated cell lines:
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Andersen LL, Mørk N, Reinert LS, Kofod-Olsen E, Narita R, Jørgensen SE, Skipper KA, Höning K, Gad HH, Østergaard L, Ørntoft TF, Hornung V, Paludan SR, Mikkelsen JG, Fujita T, Christiansen M, Hartmann R, Mogensen TH
Functional IRF3 deficiency in a patient with herpes simplex encephalitis
Andersen LL et al. Functional IRF3 deficiency in a patient with herpes simplex encephalitis. . 2015-08-24. Pubmed ID: 26216125; DOI: 10.1084/jem.20142274; PMC: PMC4548062 AUi001-A 2015-08-24 2015-08-24 PubMed: 26216125 DOI: 10.1084/jem.20142274Associated cell lines:
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Lukovic D, Artero Castro A, Delgado AB, Bernal Mde L, Luna Pelaez N, Díez Lloret A, Perez Espejo R, Kamenarova K, Fernández Sánchez L, Cuenca N, Cortón M, Avila Fernandez A, Sorkio A, Skottman H, Ayuso C, Erceg S, Bhattacharya SS
Human iPSC derived disease model of MERTK-associated retinitis pigmentosa
Lukovic D et al. Human iPSC derived disease model of MERTK-associated retinitis pigmentosa. . 2015-08-11. Pubmed ID: 26263531; DOI: 10.1038/srep12910; PMC: PMC4531787 RCPFi003-A 2015-08-11 2015-08-11 PubMed: 26263531 DOI: 10.1038/srep12910Associated cell lines:
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Kadari A, Mekala S, Wagner N, Malan D, Köth J, Doll K, Stappert L, Eckert D, Peitz M, Matthes J, Sasse P, Herzig S, Brüstle O, Ergün S, Edenhofer F
Robust Generation of Cardiomyocytes from Human iPS Cells Requires Precise Modulation of BMP and WNT Signaling
Kadari A et al. Robust Generation of Cardiomyocytes from Human iPS Cells Requires Precise Modulation of BMP and WNT Signaling. . 2015-08-00. Pubmed ID: 25392050; DOI: 10.1007/s12015-014-9564-6; PMC: PMC4493626 UKBi004-A 2015-08-00 2015-08-00 PubMed: 25392050 DOI: 10.1007/s12015-014-9564-6Associated cell lines:
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Lenzi J, De Santis R, de Turris V, Morlando M, Laneve P, Calvo A, Caliendo V, Chiò A, Rosa A, Bozzoni I
ALS mutant FUS proteins are recruited into stress granules in induced pluripotent stem cell-derived motoneurons
Lenzi J et al. ALS mutant FUS proteins are recruited into stress granules in induced pluripotent stem cell-derived motoneurons. . 2015-07-01. Pubmed ID: 26035390; DOI: 10.1242/dmm.020099; PMC: PMC4486861 SAPi002-ASAPi003-ASAPi004-A 2015-07-01 2015-07-01 PubMed: 26035390 DOI: 10.1242/dmm.020099 -
Trokovic R, Weltner J, Otonkoski T
Generation of iPSC line HEL24.3 from human neonatal foreskin fibroblasts
Trokovic R et al. Generation of iPSC line HEL24.3 from human neonatal foreskin fibroblasts. . 2015-07-00. Pubmed ID: 26093941; DOI: 10.1016/j.scr.2015.05.012 UHi006-A 2015-07-00 2015-07-00 PubMed: 26093941 DOI: 10.1016/j.scr.2015.05.012Associated cell lines:
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Trokovic R, Weltner J, Otonkoski T
Generation of iPSC line HEL47.2 from healthy human adult fibroblasts
Trokovic R et al. Generation of iPSC line HEL47.2 from healthy human adult fibroblasts. . 2015-07-00. Pubmed ID: 26096151; DOI: 10.1016/j.scr.2015.05.013 UHi007-A 2015-07-00 2015-07-00 PubMed: 26096151 DOI: 10.1016/j.scr.2015.05.013Associated cell lines:
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Zhang H, Xue C, Shah R, Bermingham K, Hinkle CC, Li W, Rodrigues A, Tabita-Martinez J, Millar JS, Cuchel M, Pashos EE, Liu Y, Yan R, Yang W, Gosai SJ, VanDorn D, Chou ST, Gregory BD, Morrisey EE, Li M, Rader DJ, Reilly MP
Functional analysis and transcriptomic profiling of iPSC-derived macrophages and their application in modeling Mendelian disease
Zhang H et al. Functional analysis and transcriptomic profiling of iPSC-derived macrophages and their application in modeling Mendelian disease. . 2015-06-19. Pubmed ID: 25904599; DOI: 10.1161/circresaha.117.305860; PMC: PMC4565503 PENNi001-A 2015-06-19 2015-06-19 PubMed: 25904599 DOI: 10.1161/circresaha.117.305860Associated cell lines:
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Tanaka Y, Hysolli E, Su J, Xiang Y, Kim KY, Zhong M, Li Y, Heydari K, Euskirchen G, Snyder MP, Pan X, Weissman SM, Park IH
Transcriptome Signature and Regulation in Human Somatic Cell Reprogramming
Tanaka Y et al. Transcriptome Signature and Regulation in Human Somatic Cell Reprogramming. . 2015-06-09. Pubmed ID: 26004630; DOI: 10.1016/j.stemcr.2015.04.009; PMC: PMC4471828 HVRDi004-B 2015-06-09 2015-06-09 PubMed: 26004630 DOI: 10.1016/j.stemcr.2015.04.009Associated cell lines:
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Shaltouki A, Sivapatham R, Pei Y, Gerencser AA, Momčilović O, Rao MS, Zeng X
Mitochondrial alterations by PARKIN in dopaminergic neurons using PARK2 patient-specific and PARK2 knockout isogenic iPSC lines
Shaltouki A et al. Mitochondrial alterations by PARKIN in dopaminergic neurons using PARK2 patient-specific and PARK2 knockout isogenic iPSC lines. . 2015-05-12. Pubmed ID: 25843045; DOI: 10.1016/j.stemcr.2015.02.019; PMC: PMC4437475 CRMi003-A-1 2015-05-12 2015-05-12 PubMed: 25843045 DOI: 10.1016/j.stemcr.2015.02.019Associated cell lines:
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Bosman A, Letourneau A, Sartiani L, Del Lungo M, Ronzoni F, Kuziakiv R, Tohonen V, Zucchelli M, Santoni F, Guipponi M, Dumevska B, Hovatta O, Antonarakis SE, Jaconi ME
Perturbations of heart development and function in cardiomyocytes from human embryonic stem cells with trisomy 21
Bosman A et al. Perturbations of heart development and function in cardiomyocytes from human embryonic stem cells with trisomy 21. . 2015-05-00. Pubmed ID: 25645121; DOI: 10.1002/stem.1961 GENEAe016-AGENEAe017-AGENEAe021-A 2015-05-00 2015-05-00 PubMed: 25645121 DOI: 10.1002/stem.1961Associated cell lines:
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Gramlich M, Pane LS, Zhou Q, Chen Z, Murgia M, Schötterl S, Goedel A, Metzger K, Brade T, Parrotta E, Schaller M, Gerull B, Thierfelder L, Aartsma-Rus A, Labeit S, Atherton JJ, McGaughran J, Harvey RP, Sinnecker D, Mann M, Laugwitz KL, Gawaz MP, Moretti A
Antisense-mediated exon skipping: a therapeutic strategy for titin-based dilated cardiomyopathy
Gramlich M et al. Antisense-mediated exon skipping: a therapeutic strategy for titin-based dilated cardiomyopathy. . 2015-05-00. Pubmed ID: 25759365; DOI: 10.15252/emmm.201505047; PMC: PMC4492817 MRIi001-AMRIi010-A 2015-05-00 2015-05-00 PubMed: 25759365 DOI: 10.15252/emmm.201505047 -
Jenny
Preimplantation Genetic Screening
Jenny. Preimplantation Genetic Screening. . 2015-04-15. CEBe002-A 2015-04-15 2015-04-15Associated cell lines:
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Pei Y, Sierra G, Sivapatham R, Swistowski A, Rao MS, Zeng X
A platform for rapid generation of single and multiplexed reporters in human iPSC lines
Pei Y et al. A platform for rapid generation of single and multiplexed reporters in human iPSC lines. . 2015-03-17. Pubmed ID: 25777362; DOI: 10.1038/srep09205; PMC: PMC4361878 CRMi003-A-1 2015-03-17 2015-03-17 PubMed: 25777362 DOI: 10.1038/srep09205Associated cell lines:
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Imberti B, Tomasoni S, Ciampi O, Pezzotta A, Derosas M, Xinaris C, Rizzo P, Papadimou E, Novelli R, Benigni A, Remuzzi G, Morigi M
Renal progenitors derived from human iPSCs engraft and restore function in a mouse model of acute kidney injury
Imberti B et al. Renal progenitors derived from human iPSCs engraft and restore function in a mouse model of acute kidney injury. . 2015-03-06. Pubmed ID: 25744951; DOI: 10.1038/srep08826; PMC: PMC4351529 IRFMNi001-AIRFMNi001-B 2015-03-06 2015-03-06 PubMed: 25744951 DOI: 10.1038/srep08826Associated cell lines:
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Toyoda T, Mae S, Tanaka H, Kondo Y, Funato M, Hosokawa Y, Sudo T, Kawaguchi Y, Osafune K
Cell aggregation optimizes the differentiation of human ESCs and iPSCs into pancreatic bud-like progenitor cells
Toyoda T et al. Cell aggregation optimizes the differentiation of human ESCs and iPSCs into pancreatic bud-like progenitor cells. . 2015-03-00. Pubmed ID: 25665923; DOI: 10.1016/j.scr.2015.01.007 KUIMSe003-ACIRAi007-A 2015-03-00 2015-03-00 PubMed: 25665923 DOI: 10.1016/j.scr.2015.01.007Associated cell lines:
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Müller-Kuller U, Ackermann M, Kolodziej S, Brendel C, Fritsch J, Lachmann N, Kunkel H, Lausen J, Schambach A, Moritz T, Grez M
A minimal ubiquitous chromatin opening element (UCOE) effectively prevents silencing of juxtaposed heterologous promoters by epigenetic remodeling in multipotent and pluripotent stem cells
Müller-Kuller U et al. A minimal ubiquitous chromatin opening element (UCOE) effectively prevents silencing of juxtaposed heterologous promoters by epigenetic remodeling in multipotent and pluripotent stem cells. . 2015-02-18. Pubmed ID: 25605798; DOI: 10.1093/nar/gkv019; PMC: PMC4330381 MHHi015-B 2015-02-18 2015-02-18 PubMed: 25605798 DOI: 10.1093/nar/gkv019Associated cell lines:
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Lachmann N, Ackermann M, Frenzel E, Liebhaber S, Brennig S, Happle C, Hoffmann D, Klimenkova O, Lüttge D, Buchegger T, Kühnel MP, Schambach A, Janciauskiene S, Figueiredo C, Hansen G, Skokowa J, Moritz T
Large-scale hematopoietic differentiation of human induced pluripotent stem cells provides granulocytes or macrophages for cell replacement therapies
Lachmann N et al. Large-scale hematopoietic differentiation of human induced pluripotent stem cells provides granulocytes or macrophages for cell replacement therapies. . 2015-02-10. Pubmed ID: 25680479; DOI: 10.1016/j.stemcr.2015.01.005; PMC: PMC4325194 MHHi015-AMHHi015-B 2015-02-10 2015-02-10 PubMed: 25680479 DOI: 10.1016/j.stemcr.2015.01.005 -
Adamo A, Atashpaz S, Germain PL, Zanella M, D'Agostino G, Albertin V, Chenoweth J, Micale L, Fusco C, Unger C, Augello B, Palumbo O, Hamilton B, Carella M, Donti E, Pruneri G, Selicorni A, Biamino E, Prontera P, McKay R, Merla G, Testa G
7q11.23 dosage-dependent dysregulation in human pluripotent stem cells affects transcriptional programs in disease-relevant lineages
Adamo A et al. 7q11.23 dosage-dependent dysregulation in human pluripotent stem cells affects transcriptional programs in disease-relevant lineages. . 2015-02-00. Pubmed ID: 25501393; DOI: 10.1038/ng.3169 UOSi001-AUOSi001-B 2015-02-00 2015-02-00 PubMed: 25501393 DOI: 10.1038/ng.3169 -
Irie N, Weinberger L, Tang WW, Kobayashi T, Viukov S, Manor YS, Dietmann S, Hanna JH, Surani MA
SOX17 is a critical specifier of human primordial germ cell fate
Irie N et al. SOX17 is a critical specifier of human primordial germ cell fate. . 2015-01-15. Pubmed ID: 25543152; DOI: 10.1016/j.cell.2014.12.013; PMC: PMC4310934 WISe001-A 2015-01-15 2015-01-15 PubMed: 25543152 DOI: 10.1016/j.cell.2014.12.013Associated cell lines:
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McCracken KW, Catá EM, Crawford CM, Sinagoga KL, Schumacher M, Rockich BE, Tsai YH, Mayhew CN, Spence JR, Zavros Y, Wells JM
Modelling human development and disease in pluripotent stem-cell-derived gastric organoids
McCracken KW et al. Modelling human development and disease in pluripotent stem-cell-derived gastric organoids. . 2014-12-18. Pubmed ID: 25363776; DOI: 10.1038/nature13863; PMC: PMC4270898 CCHMCi001-ACUSTOMi001-A 2014-12-18 2014-12-18 PubMed: 25363776 DOI: 10.1038/nature13863Associated cell lines:
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Zhang M, D'Aniello C, Verkerk AO, Wrobel E, Frank S, Ward-van Oostwaard D, Piccini I, Freund C, Rao J, Seebohm G, Atsma DE, Schulze-Bahr E, Mummery CL, Greber B, Bellin M
Recessive cardiac phenotypes in induced pluripotent stem cell models of Jervell and Lange-Nielsen syndrome: disease mechanisms and pharmacological rescue
Zhang M et al. Recessive cardiac phenotypes in induced pluripotent stem cell models of Jervell and Lange-Nielsen syndrome: disease mechanisms and pharmacological rescue. . 2014-12-16. Pubmed ID: 25453094; DOI: 10.1073/pnas.1419553111; PMC: PMC4273331 MPIi005-ALUMCi028-ALUMCi039-A 2014-12-16 2014-12-16 PubMed: 25453094 DOI: 10.1073/pnas.1419553111Associated cell lines:
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McQuade LR, Balachandran A, Scott HA, Khaira S, Baker MS, Schmidt U
Proteomics of Huntington's disease-affected human embryonic stem cells reveals an evolving pathology involving mitochondrial dysfunction and metabolic disturbances
McQuade LR et al. Proteomics of Huntington's disease-affected human embryonic stem cells reveals an evolving pathology involving mitochondrial dysfunction and metabolic disturbances. . 2014-12-05. Pubmed ID: 25316320; DOI: 10.1021/pr500649m GENEAe013-AGENEAe014-AGENEAe015-AGENEAe016-AGENEAe017-AGENEAe018-AGENEAe019-AGENEAe020-A 2014-12-05 2014-12-05 PubMed: 25316320 DOI: 10.1021/pr500649mAssociated cell lines:
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Penttinen K, Siirtola H, Àvalos-Salguero J, Vainio T, Juhola M, Aalto-Setälä K
Novel Analysis Software for Detecting and Classifying Ca2+ Transient Abnormalities in Stem Cell-Derived Cardiomyocytes
Penttinen K et al. Novel Analysis Software for Detecting and Classifying Ca2+ Transient Abnormalities in Stem Cell-Derived Cardiomyocytes. . 2015-00-00. Pubmed ID: 26308621; DOI: 10.1371/journal.pone.0135806; PMC: PMC4550257 TAUi002-ATAUi004-A 2015-00-00 2015-00-00 PubMed: 26308621 DOI: 10.1371/journal.pone.0135806 -
Lefler S, Cohen MA, Kantor G, Cheishvili D, Even A, Birger A, Turetsky T, Gil Y, Even-Ram S, Aizenman E, Bashir N, Maayan C, Razin A, Reubinoff BE, Weil M
Familial Dysautonomia (FD) Human Embryonic Stem Cell Derived PNS Neurons Reveal that Synaptic Vesicular and Neuronal Transport Genes Are Directly or Indirectly Affected by IKBKAP Downregulation
Lefler S et al. Familial Dysautonomia (FD) Human Embryonic Stem Cell Derived PNS Neurons Reveal that Synaptic Vesicular and Neuronal Transport Genes Are Directly or Indirectly Affected by IKBKAP Downregulation. . 2015-00-00. Pubmed ID: 26437462; DOI: 10.1371/journal.pone.0138807; PMC: PMC4593545 HADe004-A 2015-00-00 2015-00-00 PubMed: 26437462 DOI: 10.1371/journal.pone.0138807Associated cell lines:
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Penttinen K, Swan H, Vanninen S, Paavola J, Lahtinen AM, Kontula K, Aalto-Setälä K
Antiarrhythmic Effects of Dantrolene in Patients with Catecholaminergic Polymorphic Ventricular Tachycardia and Replication of the Responses Using iPSC Models
Penttinen K et al. Antiarrhythmic Effects of Dantrolene in Patients with Catecholaminergic Polymorphic Ventricular Tachycardia and Replication of the Responses Using iPSC Models. . 2015-00-00. Pubmed ID: 25955245; DOI: 10.1371/journal.pone.0125366; PMC: PMC4425399 TAUi002-ATAUi004-A 2015-00-00 2015-00-00 PubMed: 25955245 DOI: 10.1371/journal.pone.0125366 -
Kruse V, Hamann C, Monecke S, Cyganek L, Elsner L, Hübscher D, Walter L, Streckfuss-Bömeke K, Guan K, Dressel R
Human Induced Pluripotent Stem Cells Are Targets for Allogeneic and Autologous Natural Killer (NK) Cells and Killing Is Partly Mediated by the Activating NK Receptor DNAM-1
Kruse V et al. Human Induced Pluripotent Stem Cells Are Targets for Allogeneic and Autologous Natural Killer (NK) Cells and Killing Is Partly Mediated by the Activating NK Receptor DNAM-1. . 2015-00-00. Pubmed ID: 25950680; DOI: 10.1371/journal.pone.0125544; PMC: PMC4423859 UMGi007-AUMGi009-AUMGi011-A 2015-00-00 2015-00-00 PubMed: 25950680 DOI: 10.1371/journal.pone.0125544 -
Orban M, Goedel A, Haas J, Sandrock-Lang K, Gärtner F, Jung CB, Zieger B, Parrotta E, Kurnik K, Sinnecker D, Wanner G, Laugwitz KL, Massberg S, Moretti A
Functional comparison of induced pluripotent stem cell- and blood-derived GPIIbIIIa deficient platelets
Orban M et al. Functional comparison of induced pluripotent stem cell- and blood-derived GPIIbIIIa deficient platelets. . 2015-00-00. Pubmed ID: 25607928; DOI: 10.1371/journal.pone.0115978; PMC: PMC4301811 MRIi002-AMRIi009-A 2015-00-00 2015-00-00 PubMed: 25607928 DOI: 10.1371/journal.pone.0115978 -
Masotti A, Celluzzi A, Petrini S, Bertini E, Zanni G, Compagnucci C
Aged iPSCs display an uncommon mitochondrial appearance and fail to undergo in vitro neurogenesis
Masotti A et al. Aged iPSCs display an uncommon mitochondrial appearance and fail to undergo in vitro neurogenesis. . 2014-12-00. Pubmed ID: 25567319; DOI: 10.18632/aging.100708; PMC: PMC4298368 SBIi006-A 2014-12-00 2014-12-00 PubMed: 25567319 DOI: 10.18632/aging.100708Associated cell lines:
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Badja C, Maleeva G, El-Yazidi C, Barruet E, Lasserre M, Tropel P, Binetruy B, Bregestovski P, Magdinier F
Efficient and cost-effective generation of mature neurons from human induced pluripotent stem cells
Badja C et al. Efficient and cost-effective generation of mature neurons from human induced pluripotent stem cells. . 2014-12-00. Pubmed ID: 25355730; DOI: 10.5966/sctm.2014-0024; PMC: PMC4250204 PGNMi001-APGNMi001-A-1 2014-12-00 2014-12-00 PubMed: 25355730 DOI: 10.5966/sctm.2014-0024Associated cell lines:
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Busskamp V, Lewis NE, Guye P, Ng AH, Shipman SL, Byrne SM, Sanjana NE, Murn J, Li Y, Li S, Stadler M, Weiss R, Church GM
Rapid neurogenesis through transcriptional activation in human stem cells
Busskamp V et al. Rapid neurogenesis through transcriptional activation in human stem cells. . 2014-11-17. Pubmed ID: 25403753; DOI: 10.15252/msb.20145508; PMC: PMC4299601 HVRDi004-B-1 2014-11-17 2014-11-17 PubMed: 25403753 DOI: 10.15252/msb.20145508Associated cell lines:
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Pagliuca FW, Millman JR, Gürtler M, Segel M, Van Dervort A, Ryu JH, Peterson QP, Greiner D, Melton DA
Generation of functional human pancreatic β cells in vitro
Pagliuca FW et al. Generation of functional human pancreatic β cells in vitro. . 2014-10-09. Pubmed ID: 25303535; DOI: 10.1016/j.cell.2014.09.040; PMC: PMC4617632 HVRDi007-A 2014-10-09 2014-10-09 PubMed: 25303535 DOI: 10.1016/j.cell.2014.09.040Associated cell lines:
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Theunissen TW, Powell BE, Wang H, Mitalipova M, Faddah DA, Reddy J, Fan ZP, Maetzel D, Ganz K, Shi L, Lungjangwa T, Imsoonthornruksa S, Stelzer Y, Rangarajan S, D'Alessio A, Zhang J, Gao Q, Dawlaty MM, Young RA, Gray NS, Jaenisch R
Systematic identification of culture conditions for induction and maintenance of naive human pluripotency
Theunissen TW et al. Systematic identification of culture conditions for induction and maintenance of naive human pluripotency. . 2014-10-02. Pubmed ID: 25090446; DOI: 10.1016/j.stem.2014.07.002; PMC: PMC4184977 WIBRe001-AWIBRe002-AWIBRe001-A-1WIBRe004-AWIBRe001-A-2 2014-10-02 2014-10-02 PubMed: 25090446 DOI: 10.1016/j.stem.2014.07.002Associated cell lines:
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Yamashita A, Morioka M, Kishi H, Kimura T, Yahara Y, Okada M, Fujita K, Sawai H, Ikegawa S, Tsumaki N
Statin treatment rescues FGFR3 skeletal dysplasia phenotypes
Yamashita A et al. Statin treatment rescues FGFR3 skeletal dysplasia phenotypes. . 2014-09-25. Pubmed ID: 25231866; DOI: 10.1038/nature13775 CIRAi007-A 2014-09-25 2014-09-25 PubMed: 25231866 DOI: 10.1038/nature13775Associated cell lines:
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Rasmussen MA, Holst B, Tümer Z, Johnsen MG, Zhou S, Stummann TC, Hyttel P, Clausen C
Transient p53 suppression increases reprogramming of human fibroblasts without affecting apoptosis and DNA damage
Rasmussen MA et al. Transient p53 suppression increases reprogramming of human fibroblasts without affecting apoptosis and DNA damage. . 2014-09-09. Pubmed ID: 25241739; DOI: 10.1016/j.stemcr.2014.07.006; PMC: PMC4266010 BIONi010-ABIONi010-BBIONi010-C 2014-09-09 2014-09-09 PubMed: 25241739 DOI: 10.1016/j.stemcr.2014.07.006Associated cell lines:
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Frobel J, Hemeda H, Lenz M, Abagnale G, Joussen S, Denecke B, Sarić T, Zenke M, Wagner W
Epigenetic rejuvenation of mesenchymal stromal cells derived from induced pluripotent stem cells
Frobel J et al. Epigenetic rejuvenation of mesenchymal stromal cells derived from induced pluripotent stem cells. . 2014-09-09. Pubmed ID: 25241740; DOI: 10.1016/j.stemcr.2014.07.003; PMC: PMC4266008 UKKi006-A 2014-09-09 2014-09-09 PubMed: 25241740 DOI: 10.1016/j.stemcr.2014.07.003Associated cell lines:
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Dambrot C, Braam SR, Tertoolen LG, Birket M, Atsma DE, Mummery CL
Serum supplemented culture medium masks hypertrophic phenotypes in human pluripotent stem cell derived cardiomyocytes
Dambrot C et al. Serum supplemented culture medium masks hypertrophic phenotypes in human pluripotent stem cell derived cardiomyocytes. . 2014-08-00. Pubmed ID: 24981391; DOI: 10.1111/jcmm.12356; PMC: PMC4190898 LUMCi029-B 2014-08-00 2014-08-00 PubMed: 24981391 DOI: 10.1111/jcmm.12356Associated cell lines:
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Friedli M, Turelli P, Kapopoulou A, Rauwel B, Castro-Díaz N, Rowe HM, Ecco G, Unzu C, Planet E, Lombardo A, Mangeat B, Wildhaber BE, Naldini L, Trono D
Loss of transcriptional control over endogenous retroelements during reprogramming to pluripotency
Friedli M et al. Loss of transcriptional control over endogenous retroelements during reprogramming to pluripotency. . 2014-08-00. Pubmed ID: 24879558; DOI: 10.1101/gr.172809.114; PMC: PMC4120079 EPFLi001-AEPFLi002-AEPFLi003-AEPFLi004-AEPFLi005-AEPFLi006-A 2014-08-00 2014-08-00 PubMed: 24879558 DOI: 10.1101/gr.172809.114Associated cell lines:
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Muratore CR, Rice HC, Srikanth P, Callahan DG, Shin T, Benjamin LN, Walsh DM, Selkoe DJ, Young-Pearse TL
The familial Alzheimer's disease APPV717I mutation alters APP processing and Tau expression in iPSC-derived neurons
Muratore CR et al. The familial Alzheimer's disease APPV717I mutation alters APP processing and Tau expression in iPSC-derived neurons. . 2014-07-01. Pubmed ID: 24524897; DOI: 10.1093/hmg/ddu064; PMC: PMC4049307 HVRDi001-AHVRDi001-A-1HVRDi002-AHVRDi002-A-1 2014-07-01 2014-07-01 PubMed: 24524897 DOI: 10.1093/hmg/ddu064Associated cell lines:
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Yoshida T, Ozawa Y, Suzuki K, Yuki K, Ohyama M, Akamatsu W, Matsuzaki Y, Shimmura S, Mitani K, Tsubota K, Okano H
The use of induced pluripotent stem cells to reveal pathogenic gene mutations and explore treatments for retinitis pigmentosa
Yoshida T et al. The use of induced pluripotent stem cells to reveal pathogenic gene mutations and explore treatments for retinitis pigmentosa. . 2014-06-16. Pubmed ID: 24935155; DOI: 10.1186/1756-6606-7-45; PMC: PMC4058693 KUIFMSi004-C 2014-06-16 2014-06-16 PubMed: 24935155 DOI: 10.1186/1756-6606-7-45Associated cell lines:
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Kiskinis E, Sandoe J, Williams LA, Boulting GL, Moccia R, Wainger BJ, Han S, Peng T, Thams S, Mikkilineni S, Mellin C, Merkle FT, Davis-Dusenbery BN, Ziller M, Oakley D, Ichida J, Di Costanzo S, Atwater N, Maeder ML, Goodwin MJ, Nemesh J, Handsaker RE, Paull D, Noggle S, McCarroll SA, Joung JK, Woolf CJ, Brown RH, Eggan K
Pathways disrupted in human ALS motor neurons identified through genetic correction of mutant SOD1
Kiskinis E et al. Pathways disrupted in human ALS motor neurons identified through genetic correction of mutant SOD1. . 2014-06-05. Pubmed ID: 24704492; DOI: 10.1016/j.stem.2014.03.004; PMC: PMC4653065 HVRDi006-A 2014-06-05 2014-06-05 PubMed: 24704492 DOI: 10.1016/j.stem.2014.03.004Associated cell lines:
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Maetzel D, Sarkar S, Wang H, Abi-Mosleh L, Xu P, Cheng AW, Gao Q, Mitalipova M, Jaenisch R
Genetic and chemical correction of cholesterol accumulation and impaired autophagy in hepatic and neural cells derived from Niemann-Pick Type C patient-specific iPS cells
Maetzel D et al. Genetic and chemical correction of cholesterol accumulation and impaired autophagy in hepatic and neural cells derived from Niemann-Pick Type C patient-specific iPS cells. . 2014-06-03. Pubmed ID: 24936472; DOI: 10.1016/j.stemcr.2014.03.014; PMC: PMC4050353 WIBRe001-A 2014-06-03 2014-06-03 PubMed: 24936472 DOI: 10.1016/j.stemcr.2014.03.014Associated cell lines:
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Bradley CK, Peura T, Dumevska B, Jovasevic A, Chami O, Schmidt U, Jansen RP, Stojanov T
Cell lines from morphologically abnormal discarded IVF embryos are typically euploid and unaccompanied by intrachromosomal aberrations
Bradley CK et al. Cell lines from morphologically abnormal discarded IVF embryos are typically euploid and unaccompanied by intrachromosomal aberrations. . 2014-06-00. Pubmed ID: 24745836; DOI: 10.1016/j.rbmo.2014.02.001 GENEAe014-A 2014-06-00 2014-06-00 PubMed: 24745836 DOI: 10.1016/j.rbmo.2014.02.001Associated cell lines:
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Sterthaus O, Feutz AC, Zhang H, Pletscher F, Bruder E, Miny P, Lezzi G, De Geyter M, De Geyter C
Gene expression profiles of similarly derived human embryonic stem cell lines correlate with their distinct propensity to exit stemness and their different differentiation behavior in culture
Sterthaus O et al. Gene expression profiles of similarly derived human embryonic stem cell lines correlate with their distinct propensity to exit stemness and their different differentiation behavior in culture. . 2014-06-00. Pubmed ID: 24811852; DOI: 10.1089/cell.2013.0089 UBASe001-AUBASe002-AUBASe003-A 2014-06-00 2014-06-00 PubMed: 24811852 DOI: 10.1089/cell.2013.0089Associated cell lines:
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Letourneau A, Santoni FA, Bonilla X, Sailani MR, Gonzalez D, Kind J, Chevalier C, Thurman R, Sandstrom RS, Hibaoui Y, Garieri M, Popadin K, Falconnet E, Gagnebin M, Gehrig C, Vannier A, Guipponi M, Farinelli L, Robyr D, Migliavacca E, Borel C, Deutsch S, Feki A, Stamatoyannopoulos JA, Herault Y, van Steensel B, Guigo R, Antonarakis SE
Domains of genome-wide gene expression dysregulation in Down's syndrome
Letourneau A et al. Domains of genome-wide gene expression dysregulation in Down's syndrome. . 2014-04-17. Pubmed ID: 24740065; DOI: 10.1038/nature13200 UNIGEi004-A 2014-04-17 2014-04-17 PubMed: 24740065 DOI: 10.1038/nature13200Associated cell lines:
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Ahola A, Kiviaho AL, Larsson K, Honkanen M, Aalto-Setälä K, Hyttinen J
Video image-based analysis of single human induced pluripotent stem cell derived cardiomyocyte beating dynamics using digital image correlation
Ahola A et al. Video image-based analysis of single human induced pluripotent stem cell derived cardiomyocyte beating dynamics using digital image correlation. . 2014-04-07. Pubmed ID: 24708714; DOI: 10.1186/1475-925x-13-39; PMC: PMC3984432 TAUi002-A 2014-04-07 2014-04-07 PubMed: 24708714 DOI: 10.1186/1475-925x-13-39Associated cell lines:
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Miyaoka Y, Chan AH, Judge LM, Yoo J, Huang M, Nguyen TD, Lizarraga PP, So PL, Conklin BR
Isolation of single-base genome-edited human iPS cells without antibiotic selection
Miyaoka Y et al. Isolation of single-base genome-edited human iPS cells without antibiotic selection. . 2014-03-00. Pubmed ID: 24509632; DOI: 10.1038/nmeth.2840; PMC: PMC4063274 UCSFi001-A 2014-03-00 2014-03-00 PubMed: 24509632 DOI: 10.1038/nmeth.2840Associated cell lines:
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Mallon BS, Hamilton RS, Kozhich OA, Johnson KR, Fann YC, Rao MS, Robey PG
Comparison of the molecular profiles of human embryonic and induced pluripotent stem cells of isogenic origin
Mallon BS et al. Comparison of the molecular profiles of human embryonic and induced pluripotent stem cells of isogenic origin. . 2014-03-00. Pubmed ID: 24374290; DOI: 10.1016/j.scr.2013.11.010; PMC: PMC4157340 WAe001-A 2014-03-00 2014-03-00 PubMed: 24374290 DOI: 10.1016/j.scr.2013.11.010Associated cell lines:
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Alami NH, Smith RB, Carrasco MA, Williams LA, Winborn CS, Han SSW, Kiskinis E, Winborn B, Freibaum BD, Kanagaraj A, Clare AJ, Badders NM, Bilican B, Chaum E, Chandran S, Shaw CE, Eggan KC, Maniatis T, Taylor JP
Axonal transport of TDP-43 mRNA granules is impaired by ALS-causing mutations
Alami NH et al. Axonal transport of TDP-43 mRNA granules is impaired by ALS-causing mutations. . 2014-02-05. Pubmed ID: 24507191; DOI: 10.1016/j.neuron.2013.12.018; PMC: PMC3939050 HVRDi014-A 2014-02-05 2014-02-05 PubMed: 24507191 DOI: 10.1016/j.neuron.2013.12.018Associated cell lines:
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Hibaoui Y, Grad I, Letourneau A, Sailani MR, Dahoun S, Santoni FA, Gimelli S, Guipponi M, Pelte MF, Béna F, Antonarakis SE, Feki A
Modelling and rescuing neurodevelopmental defect of Down syndrome using induced pluripotent stem cells from monozygotic twins discordant for trisomy 21
Hibaoui Y et al. Modelling and rescuing neurodevelopmental defect of Down syndrome using induced pluripotent stem cells from monozygotic twins discordant for trisomy 21. . 2014-02-00. Pubmed ID: 24375627; DOI: 10.1002/emmm.201302848; PMC: PMC3927959 UNIGEi002-AUNIGEi004-A 2014-02-00 2014-02-00 PubMed: 24375627 DOI: 10.1002/emmm.201302848Associated cell lines:
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Ackermann M, Lachmann N, Hartung S, Eggenschwiler R, Pfaff N, Happle C, Mucci A, Göhring G, Niemann H, Hansen G, Schambach A, Cantz T, Zweigerdt R, Moritz T
Promoter and lineage independent anti-silencing activity of the A2 ubiquitous chromatin opening element for optimized human pluripotent stem cell-based gene therapy
Ackermann M et al. Promoter and lineage independent anti-silencing activity of the A2 ubiquitous chromatin opening element for optimized human pluripotent stem cell-based gene therapy. . 2014-02-00. Pubmed ID: 24290698; DOI: 10.1016/j.biomaterials.2013.11.024 MHHi015-AMHHi015-B 2014-02-00 2014-02-00 PubMed: 24290698 DOI: 10.1016/j.biomaterials.2013.11.024 -
Vitaloni M, Pulecio J, Bilic J, Kuebler B, Laricchia-Robbio L, Izpisua Belmonte JC
MicroRNAs contribute to induced pluripotent stem cell somatic donor memory
Vitaloni M et al. MicroRNAs contribute to induced pluripotent stem cell somatic donor memory. . 2014-01-24. Pubmed ID: 24311783; DOI: 10.1074/jbc.m113.538702; PMC: PMC3900956 ESi041-AESi041-BESi041-C 2014-01-24 2014-01-24 PubMed: 24311783 DOI: 10.1074/jbc.m113.538702 -
Lachmann N, Happle C, Ackermann M, Lüttge D, Wetzke M, Merkert S, Hetzel M, Kensah G, Jara-Avaca M, Mucci A, Skuljec J, Dittrich AM, Pfaff N, Brennig S, Schambach A, Steinemann D, Göhring G, Cantz T, Martin U, Schwerk N, Hansen G, Moritz T
Gene correction of human induced pluripotent stem cells repairs the cellular phenotype in pulmonary alveolar proteinosis
Lachmann N et al. Gene correction of human induced pluripotent stem cells repairs the cellular phenotype in pulmonary alveolar proteinosis. . 2014-01-15. Pubmed ID: 24279725; DOI: 10.1164/rccm.201306-1012oc MHHi015-A 2014-01-15 2014-01-15 PubMed: 24279725 DOI: 10.1164/rccm.201306-1012ocAssociated cell lines:
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Gerhardt J, Tomishima MJ, Zaninovic N, Colak D, Yan Z, Zhan Q, Rosenwaks Z, Jaffrey SR, Schildkraut CL
The DNA replication program is altered at the FMR1 locus in fragile X embryonic stem cells
Gerhardt J et al. The DNA replication program is altered at the FMR1 locus in fragile X embryonic stem cells. . 2014-01-09. Pubmed ID: 24289922; DOI: 10.1016/j.molcel.2013.10.029; PMC: PMC3920742 RGIe116-A 2014-01-09 2014-01-09 PubMed: 24289922 DOI: 10.1016/j.molcel.2013.10.029Associated cell lines:
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Nakagawa M, Taniguchi Y, Senda S, Takizawa N, Ichisaka T, Asano K, Morizane A, Doi D, Takahashi J, Nishizawa M, Yoshida Y, Toyoda T, Osafune K, Sekiguchi K, Yamanaka S
A novel efficient feeder-free culture system for the derivation of human induced pluripotent stem cells
Nakagawa M et al. A novel efficient feeder-free culture system for the derivation of human induced pluripotent stem cells. . 2014-01-08. Pubmed ID: 24399248; DOI: 10.1038/srep03594; PMC: PMC3884228 KUIFMSi004-BKUIFMSi004-C 2014-01-08 2014-01-08 PubMed: 24399248 DOI: 10.1038/srep03594Associated cell lines:
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Koyanagi-Aoi M, Ohnuki M, Takahashi K, Okita K, Noma H, Sawamura Y, Teramoto I, Narita M, Sato Y, Ichisaka T, Amano N, Watanabe A, Morizane A, Yamada Y, Sato T, Takahashi J, Yamanaka S
Differentiation-defective phenotypes revealed by large-scale analyses of human pluripotent stem cells
Koyanagi-Aoi M et al. Differentiation-defective phenotypes revealed by large-scale analyses of human pluripotent stem cells. . 2013-12-17. Pubmed ID: 24259714; DOI: 10.1073/pnas.1319061110; PMC: PMC3870695 WAe001-AWAe009-AESIBIe003-AESIBIe004-AKUIMSe001-AKUIMSe003-ACEBe034-AESIBIe006-AKUIFMSi004-DKUIFMSi004-BKUIFMSi004-CKUIFMSi011-ACIRAi007-A 2013-12-17 2013-12-17 PubMed: 24259714 DOI: 10.1073/pnas.1319061110Associated cell lines:
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Gafni O, Weinberger L, Mansour AA, Manor YS, Chomsky E, Ben-Yosef D, Kalma Y, Viukov S, Maza I, Zviran A, Rais Y, Shipony Z, Mukamel Z, Krupalnik V, Zerbib M, Geula S, Caspi I, Schneir D, Shwartz T, Gilad S, Amann-Zalcenstein D, Benjamin S, Amit I, Tanay A, Massarwa R, Novershtern N, Hanna JH
Derivation of novel human ground state naive pluripotent stem cells
Gafni O et al. Derivation of novel human ground state naive pluripotent stem cells. . 2013-12-12. Pubmed ID: 24172903; DOI: 10.1038/nature12745 VIACe001-AWIBRe001-AWISi006-A 2013-12-12 2013-12-12 PubMed: 24172903 DOI: 10.1038/nature12745Associated cell lines:
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Bellin M, Casini S, Davis RP, D'Aniello C, Haas J, Ward-van Oostwaard D, Tertoolen LG, Jung CB, Elliott DA, Welling A, Laugwitz KL, Moretti A, Mummery CL
Isogenic human pluripotent stem cell pairs reveal the role of a KCNH2 mutation in long-QT syndrome
Bellin M et al. Isogenic human pluripotent stem cell pairs reveal the role of a KCNH2 mutation in long-QT syndrome. . 2013-12-11. Pubmed ID: 24213244; DOI: 10.1038/emboj.2013.240; PMC: PMC3981141 MRIi006-A 2013-12-11 2013-12-11 PubMed: 24213244 DOI: 10.1038/emboj.2013.240Associated cell lines:
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Warlich E, Schambach A, Lock D, Wedekind D, Glage S, Eckardt D, Bosio A, Knöbel S
FAS-based cell depletion facilitates the selective isolation of mouse induced pluripotent stem cells
Warlich E et al. FAS-based cell depletion facilitates the selective isolation of mouse induced pluripotent stem cells. . 2014-00-00. Pubmed ID: 25029550; DOI: 10.1371/journal.pone.0102171; PMC: PMC4100888 MILi001-A 2014-00-00 2014-00-00 PubMed: 25029550 DOI: 10.1371/journal.pone.0102171Associated cell lines:
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Wattanapanitch M, Klincumhom N, Potirat P, Amornpisutt R, Lorthongpanich C, U-pratya Y, Laowtammathron C, Kheolamai P, Poungvarin N, Issaragrisil S
Dual small-molecule targeting of SMAD signaling stimulates human induced pluripotent stem cells toward neural lineages
Wattanapanitch M et al. Dual small-molecule targeting of SMAD signaling stimulates human induced pluripotent stem cells toward neural lineages. . 2014-00-00. Pubmed ID: 25207966; DOI: 10.1371/journal.pone.0106952; PMC: PMC4160199 MUSIi009-A 2014-00-00 2014-00-00 PubMed: 25207966 DOI: 10.1371/journal.pone.0106952Associated cell lines:
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Lim ML, Jungebluth P, Sjöqvist S, Nikdin H, Kjartansdóttir KR, Unger C, Vassliev I, Macchiarini P
Decellularized feeders: an optimized method for culturing pluripotent cells
Lim ML et al. Decellularized feeders: an optimized method for culturing pluripotent cells. . 2013-12-00. Pubmed ID: 24167316; DOI: 10.5966/sctm.2013-0077; PMC: PMC3841092 UOSi001-A 2013-12-00 2013-12-00 PubMed: 24167316 DOI: 10.5966/sctm.2013-0077Associated cell lines:
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Rodin S, Antonsson L, Niaudet C, Simonson OE, Salmela E, Hansson EM, Domogatskaya A, Xiao Z, Damdimopoulou P, Sheikhi M, Inzunza J, Nilsson AS, Baker D, Kuiper R, Sun Y, Blennow E, Nordenskjöld M, Grinnemo KH, Kere J, Betsholtz C, Hovatta O, Tryggvason K
Clonal culturing of human embryonic stem cells on laminin-521/E-cadherin matrix in defined and xeno-free environment
Rodin S et al. Clonal culturing of human embryonic stem cells on laminin-521/E-cadherin matrix in defined and xeno-free environment. . 2014-00-00. Pubmed ID: 24463987; DOI: 10.1038/ncomms4195 KIe001-AKIe019-AKIe032-AKIe033-AKIe051-AKIe053-AKIe054-AKIe055-A 2014-00-00 2014-00-00 PubMed: 24463987 DOI: 10.1038/ncomms4195 -
Flierl A, Oliveira LM, Falomir-Lockhart LJ, Mak SK, Hesley J, Soldner F, Arndt-Jovin DJ, Jaenisch R, Langston JW, Jovin TM, Schüle B
Higher vulnerability and stress sensitivity of neuronal precursor cells carrying an alpha-synuclein gene triplication
Flierl A et al. Higher vulnerability and stress sensitivity of neuronal precursor cells carrying an alpha-synuclein gene triplication. . 2014-00-00. Pubmed ID: 25390032; DOI: 10.1371/journal.pone.0112413; PMC: PMC4229205 SUSMi005-A 2014-00-00 2014-00-00 PubMed: 25390032 DOI: 10.1371/journal.pone.0112413Associated cell lines:
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Chung CY, Khurana V, Auluck PK, Tardiff DF, Mazzulli JR, Soldner F, Baru V, Lou Y, Freyzon Y, Cho S, Mungenast AE, Muffat J, Mitalipova M, Pluth MD, Jui NT, Schüle B, Lippard SJ, Tsai LH, Krainc D, Buchwald SL, Jaenisch R, Lindquist S
Identification and rescue of α-synuclein toxicity in Parkinson patient-derived neurons
Chung CY et al. Identification and rescue of α-synuclein toxicity in Parkinson patient-derived neurons. . 2013-11-22. Pubmed ID: 24158904; DOI: 10.1126/science.1245296; PMC: PMC4022187 SUSMi005-A 2013-11-22 2013-11-22 PubMed: 24158904 DOI: 10.1126/science.1245296Associated cell lines:
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Auré K, Dubourg O, Jardel C, Clarysse L, Sternberg D, Fournier E, Laforêt P, Streichenberger N, Petiot P, Gervais-Bernard H, Vial C, Bedat-Millet AL, Drouin-Garraud V, Bouillaud F, Vandier C, Fontaine B, Lombès A
Episodic weakness due to mitochondrial DNA MT-ATP6/8 mutations
Auré K et al. Episodic weakness due to mitochondrial DNA MT-ATP6/8 mutations. . 2013-11-19. Pubmed ID: 24153443; DOI: 10.1212/01.wnl.0000436067.43384.0b HHUi001-AHHUi002-A 2013-11-19 2013-11-19 PubMed: 24153443 DOI: 10.1212/01.wnl.0000436067.43384.0b -
Cappello S, Gray MJ, Badouel C, Lange S, Einsiedler M, Srour M, Chitayat D, Hamdan FF, Jenkins ZA, Morgan T, Preitner N, Uster T, Thomas J, Shannon P, Morrison V, Di Donato N, Van Maldergem L, Neuhann T, Newbury-Ecob R, Swinkells M, Terhal P, Wilson LC, Zwijnenburg PJ, Sutherland-Smith AJ, Black MA, Markie D, Michaud JL, Simpson MA, Mansour S, McNeill H, Götz M, Robertson SP
Mutations in genes encoding the cadherin receptor-ligand pair DCHS1 and FAT4 disrupt cerebral cortical development
Cappello S et al. Mutations in genes encoding the cadherin receptor-ligand pair DCHS1 and FAT4 disrupt cerebral cortical development. . 2013-11-00. Pubmed ID: 24056717; DOI: 10.1038/ng.2765 ISFi003-AISFi004-A 2013-11-00 2013-11-00 PubMed: 24056717 DOI: 10.1038/ng.2765 -
Donnelly CJ, Zhang PW, Pham JT, Haeusler AR, Mistry NA, Vidensky S, Daley EL, Poth EM, Hoover B, Fines DM, Maragakis N, Tienari PJ, Petrucelli L, Traynor BJ, Wang J, Rigo F, Bennett CF, Blackshaw S, Sattler R, Rothstein JD
RNA toxicity from the ALS/FTD C9ORF72 expansion is mitigated by antisense intervention
Donnelly CJ et al. RNA toxicity from the ALS/FTD C9ORF72 expansion is mitigated by antisense intervention. . 2013-10-16. Pubmed ID: 24139042; DOI: 10.1016/j.neuron.2013.10.015; PMC: PMC4098943 UHi002-AUHi003-A 2013-10-16 2013-10-16 PubMed: 24139042 DOI: 10.1016/j.neuron.2013.10.015 -
Ulvestad M, Nordell P, Asplund A, Rehnström M, Jacobsson S, Holmgren G, Davidson L, Brolén G, Edsbagge J, Björquist P, Küppers-Munther B, Andersson TB
Drug metabolizing enzyme and transporter protein profiles of hepatocytes derived from human embryonic and induced pluripotent stem cells
Ulvestad M et al. Drug metabolizing enzyme and transporter protein profiles of hepatocytes derived from human embryonic and induced pluripotent stem cells. . 2013-09-01. Pubmed ID: 23856292; DOI: 10.1016/j.bcp.2013.06.029 CEBe015-AUODi001-A 2013-09-01 2013-09-01 PubMed: 23856292 DOI: 10.1016/j.bcp.2013.06.029 -
Dudek J, Cheng IF, Balleininger M, Vaz FM, Streckfuss-Bömeke K, Hübscher D, Vukotic M, Wanders RJ, Rehling P, Guan K
Cardiolipin deficiency affects respiratory chain function and organization in an induced pluripotent stem cell model of Barth syndrome
Dudek J et al. Cardiolipin deficiency affects respiratory chain function and organization in an induced pluripotent stem cell model of Barth syndrome. . 2013-09-00. Pubmed ID: 23792436; DOI: 10.1016/j.scr.2013.05.005 UMGi054-AUMGi055-AUMGi056-A 2013-09-00 2013-09-00 PubMed: 23792436 DOI: 10.1016/j.scr.2013.05.005 -
Streckfuss-Bömeke K, Wolf F, Azizian A, Stauske M, Tiburcy M, Wagner S, Hübscher D, Dressel R, Chen S, Jende J, Wulf G, Lorenz V, Schön MP, Maier LS, Zimmermann WH, Hasenfuss G, Guan K
Comparative study of human-induced pluripotent stem cells derived from bone marrow cells, hair keratinocytes, and skin fibroblasts
Streckfuss-Bömeke K et al. Comparative study of human-induced pluripotent stem cells derived from bone marrow cells, hair keratinocytes, and skin fibroblasts. . 2013-09-00. Pubmed ID: 22798560; DOI: 10.1093/eurheartj/ehs203 UMGi001-AUMGi002-AUMGi003-AUMGi004-AUMGi005-AUMGi006-AUMGi007-AUMGi008-AUMGi009-AUMGi010-AUMGi012-A 2013-09-00 2013-09-00 PubMed: 22798560 DOI: 10.1093/eurheartj/ehs203 -
Zhang XH, Haviland S, Wei H, Sarić T, Fatima A, Hescheler J, Cleemann L, Morad M
Ca2+ signaling in human induced pluripotent stem cell-derived cardiomyocytes (iPS-CM) from normal and catecholaminergic polymorphic ventricular tachycardia (CPVT)-afflicted subjects
Zhang XH et al. Ca2+ signaling in human induced pluripotent stem cell-derived cardiomyocytes (iPS-CM) from normal and catecholaminergic polymorphic ventricular tachycardia (CPVT)-afflicted subjects. . 2013-08-00. Pubmed ID: 23684427; DOI: 10.1016/j.ceca.2013.04.004; PMC: PMC3781932 UKKi007-AUKKi007-B 2013-08-00 2013-08-00 PubMed: 23684427 DOI: 10.1016/j.ceca.2013.04.004 -
Tang Z, Berlin DS, Toji L, Toruner GA, Beiswanger C, Kulkarni S, Martin CL, Emanuel BS, Christman M, Gerry NP
A dynamic database of microarray-characterized cell lines with various cytogenetic and genomic backgrounds
Tang Z et al. A dynamic database of microarray-characterized cell lines with various cytogenetic and genomic backgrounds. . 2013-07-08. Pubmed ID: 23665875; DOI: 10.1534/g3.113.006577; PMC: PMC3704242 KAUSTi001-AKAUSTi001-B 2013-07-08 2013-07-08 PubMed: 23665875 DOI: 10.1534/g3.113.006577Associated cell lines:
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Weick JP, Held DL, Bonadurer GF 3rd, Doers ME, Liu Y, Maguire C, Clark A, Knackert JA, Molinarolo K, Musser M, Yao L, Yin Y, Lu J, Zhang X, Zhang SC, Bhattacharyya A
Deficits in human trisomy 21 iPSCs and neurons
Weick JP et al. Deficits in human trisomy 21 iPSCs and neurons. . 2013-06-11. Pubmed ID: 23716668; DOI: 10.1073/pnas.1216575110; PMC: PMC3683748 WISCi005-AWISCi006-AWISCi005-BWISCi005-C 2013-06-11 2013-06-11 PubMed: 23716668 DOI: 10.1073/pnas.1216575110Associated cell lines:
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Higurashi N, Uchida T, Lossin C, Misumi Y, Okada Y, Akamatsu W, Imaizumi Y, Zhang B, Nabeshima K, Mori MX, Katsurabayashi S, Shirasaka Y, Okano H, Hirose S
A human Dravet syndrome model from patient induced pluripotent stem cells
Higurashi N et al. A human Dravet syndrome model from patient induced pluripotent stem cells. . 2013-05-02. Pubmed ID: 23639079; DOI: 10.1186/1756-6606-6-19; PMC: PMC3655893 FUi001-B 2013-05-02 2013-05-02 PubMed: 23639079 DOI: 10.1186/1756-6606-6-19Associated cell lines:
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Kiely AP, Asi YT, Kara E, Limousin P, Ling H, Lewis P, Proukakis C, Quinn N, Lees AJ, Hardy J, Revesz T, Houlden H, Holton JL
α-Synucleinopathy associated with G51D SNCA mutation: a link between Parkinson's disease and multiple system atrophy?
Kiely AP et al. α-Synucleinopathy associated with G51D SNCA mutation: a link between Parkinson's disease and multiple system atrophy?. . 2013-05-00. Pubmed ID: 23404372; DOI: 10.1007/s00401-013-1096-7; PMC: PMC3681325 EDi008-B 2013-05-00 2013-05-00 PubMed: 23404372 DOI: 10.1007/s00401-013-1096-7Associated cell lines:
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Kondo T, Asai M, Tsukita K, Kutoku Y, Ohsawa Y, Sunada Y, Imamura K, Egawa N, Yahata N, Okita K, Takahashi K, Asaka I, Aoi T, Watanabe A, Watanabe K, Kadoya C, Nakano R, Watanabe D, Maruyama K, Hori O, Hibino S, Choshi T, Nakahata T, Hioki H, Kaneko T, Naitoh M, Yoshikawa K, Yamawaki S, Suzuki S, Hata R, Ueno S, Seki T, Kobayashi K, Toda T, Murakami K, Irie K, Klein WL, Mori H, Asada T, Takahashi R, Iwata N, Yamanaka S, Inoue H
Modeling Alzheimer's disease with iPSCs reveals stress phenotypes associated with intracellular Aβ and differential drug responsiveness
Kondo T et al. Modeling Alzheimer's disease with iPSCs reveals stress phenotypes associated with intracellular Aβ and differential drug responsiveness. . 2013-04-04. Pubmed ID: 23434393; DOI: 10.1016/j.stem.2013.01.009 CIRAi007-A 2013-04-04 2013-04-04 PubMed: 23434393 DOI: 10.1016/j.stem.2013.01.009Associated cell lines:
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Reinhardt P, Schmid B, Burbulla LF, Schöndorf DC, Wagner L, Glatza M, Höing S, Hargus G, Heck SA, Dhingra A, Wu G, Müller S, Brockmann K, Kluba T, Maisel M, Krüger R, Berg D, Tsytsyura Y, Thiel CS, Psathaki OE, Klingauf J, Kuhlmann T, Klewin M, Müller H, Gasser T, Schöler HR, Sterneckert J
Genetic correction of a LRRK2 mutation in human iPSCs links parkinsonian neurodegeneration to ERK-dependent changes in gene expression
Reinhardt P et al. Genetic correction of a LRRK2 mutation in human iPSCs links parkinsonian neurodegeneration to ERK-dependent changes in gene expression. . 2013-03-07. Pubmed ID: 23472874; DOI: 10.1016/j.stem.2013.01.008 CRTDi001-AMPIi002-AMPIi003-AMPIi003-A-1 2013-03-07 2013-03-07 PubMed: 23472874 DOI: 10.1016/j.stem.2013.01.008Associated cell lines:
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Mikkola M, Toivonen S, Tamminen K, Alfthan K, Tuuri T, Satomaa T, Natunen J, Saarinen J, Tiittanen M, Lampinen M, Valmu L, Partanen J, Otonkoski T
Lectin from Erythrina cristagalli supports undifferentiated growth and differentiation of human pluripotent stem cells
Mikkola M et al. Lectin from Erythrina cristagalli supports undifferentiated growth and differentiation of human pluripotent stem cells. . 2013-03-01. Pubmed ID: 23106381; DOI: 10.1089/scd.2012.0365 UHi007-B 2013-03-01 2013-03-01 PubMed: 23106381 DOI: 10.1089/scd.2012.0365Associated cell lines:
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Briggs JA, Sun J, Shepherd J, Ovchinnikov DA, Chung TL, Nayler SP, Kao LP, Morrow CA, Thakar NY, Soo SY, Peura T, Grimmond S, Wolvetang EJ
Integration-free induced pluripotent stem cells model genetic and neural developmental features of down syndrome etiology
Briggs JA et al. Integration-free induced pluripotent stem cells model genetic and neural developmental features of down syndrome etiology. . 2013-03-00. Pubmed ID: 23225669; DOI: 10.1002/stem.1297 SCSe001-A 2013-03-00 2013-03-00 PubMed: 23225669 DOI: 10.1002/stem.1297Associated cell lines:
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Varley KE, Gertz J, Bowling KM, Parker SL, Reddy TE, Pauli-Behn F, Cross MK, Williams BA, Stamatoyannopoulos JA, Crawford GE, Absher DM, Wold BJ, Myers RM
Dynamic DNA methylation across diverse human cell lines and tissues
Varley KE et al. Dynamic DNA methylation across diverse human cell lines and tissues. . 2013-03-00. Pubmed ID: 23325432; DOI: 10.1101/gr.147942.112; PMC: PMC3589544 WAe001-A 2013-03-00 2013-03-00 PubMed: 23325432 DOI: 10.1101/gr.147942.112Associated cell lines:
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Tiscornia G, Vivas EL, Matalonga L, Berniakovich I, Barragán Monasterio M, Eguizábal C, Gort L, González F, Ortiz Mellet C, García Fernández JM, Ribes A, Veiga A, Izpisua Belmonte JC
Neuronopathic Gaucher's disease: induced pluripotent stem cells for disease modelling and testing chaperone activity of small compounds
Tiscornia G et al. Neuronopathic Gaucher's disease: induced pluripotent stem cells for disease modelling and testing chaperone activity of small compounds. . 2013-02-15. Pubmed ID: 23118351; DOI: 10.1093/hmg/dds471 ESi031-C 2013-02-15 2013-02-15 PubMed: 23118351 DOI: 10.1093/hmg/dds471Associated cell lines:
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Koch CM, Reck K, Shao K, Lin Q, Joussen S, Ziegler P, Walenda G, Drescher W, Opalka B, May T, Brümmendorf T, Zenke M, Saric T, Wagner W
Pluripotent stem cells escape from senescence-associated DNA methylation changes
Koch CM et al. Pluripotent stem cells escape from senescence-associated DNA methylation changes. . 2013-02-00. Pubmed ID: 23080539; DOI: 10.1101/gr.141945.112; PMC: PMC3561866 UKKi006-A 2013-02-00 2013-02-00 PubMed: 23080539 DOI: 10.1101/gr.141945.112Associated cell lines:
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Freitas ER, Santos RL, Lima EC, Guillo LA
Feeder-free culture of human embryonic stem cell line BG01V/hOG using magnetic field-magnetic nanoparticles system
Freitas ER et al. Feeder-free culture of human embryonic stem cell line BG01V/hOG using magnetic field-magnetic nanoparticles system. . 2013-02-00. Pubmed ID: 23089476; DOI: 10.1016/j.biopha.2012.08.004 VIACe001-A-1 2013-02-00 2013-02-00 PubMed: 23089476 DOI: 10.1016/j.biopha.2012.08.004Associated cell lines:
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Toivonen S, Ojala M, Hyysalo A, Ilmarinen T, Rajala K, Pekkanen-Mattila M, Äänismaa R, Lundin K, Palgi J, Weltner J, Trokovic R, Silvennoinen O, Skottman H, Narkilahti S, Aalto-Setälä K, Otonkoski T
Comparative analysis of targeted differentiation of human induced pluripotent stem cells (hiPSCs) and human embryonic stem cells reveals variability associated with incomplete transgene silencing in retrovirally derived hiPSC lines
Toivonen S et al. Comparative analysis of targeted differentiation of human induced pluripotent stem cells (hiPSCs) and human embryonic stem cells reveals variability associated with incomplete transgene silencing in retrovirally derived hiPSC lines. . 2013-02-00. Pubmed ID: 23341440; DOI: 10.5966/sctm.2012-0047; PMC: PMC3659749 UHe003-AWAe007-AUTAe007-AUHi006-A 2013-02-00 2013-02-00 PubMed: 23341440 DOI: 10.5966/sctm.2012-0047 -
Yamana R, Iwasaki M, Wakabayashi M, Nakagawa M, Yamanaka S, Ishihama Y
Rapid and deep profiling of human induced pluripotent stem cell proteome by one-shot NanoLC-MS/MS analysis with meter-scale monolithic silica columns
Yamana R et al. Rapid and deep profiling of human induced pluripotent stem cell proteome by one-shot NanoLC-MS/MS analysis with meter-scale monolithic silica columns. . 2013-01-04. Pubmed ID: 23210603; DOI: 10.1021/pr300837u KUIFMSi004-C 2013-01-04 2013-01-04 PubMed: 23210603 DOI: 10.1021/pr300837uAssociated cell lines:
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Mallon BS, Chenoweth JG, Johnson KR, Hamilton RS, Tesar PJ, Yavatkar AS, Tyson LJ, Park K, Chen KG, Fann YC, McKay RD
StemCellDB: the human pluripotent stem cell database at the National Institutes of Health
Mallon BS et al. StemCellDB: the human pluripotent stem cell database at the National Institutes of Health. . 2013-01-00. Pubmed ID: 23117585; DOI: 10.1016/j.scr.2012.09.002; PMC: PMC3590800 TECHe001-ATECHe002-ATECHe003-AWAe001-AWAe007-AWAe009-AWAe013-AWAe014-AVIACe001-AVIACe002-AVIACe003-AESIBIe001-AESIBIe002-AESIBIe003-AESIBIe004-AESIBIe005-AUCSFe002-ACEBe033-ACEBe034-AESIBIe006-A 2013-01-00 2013-01-00 PubMed: 23117585 DOI: 10.1016/j.scr.2012.09.002 -
Shao K, Koch C, Gupta MK, Lin Q, Lenz M, Laufs S, Denecke B, Schmidt M, Linke M, Hennies HC, Hescheler J, Zenke M, Zechner U, Šarić T, Wagner W
Induced pluripotent mesenchymal stromal cell clones retain donor-derived differences in DNA methylation profiles
Shao K et al. Induced pluripotent mesenchymal stromal cell clones retain donor-derived differences in DNA methylation profiles. . 2013-01-00. Pubmed ID: 23032973; DOI: 10.1038/mt.2012.207; PMC: PMC3538313 UKKi006-A 2013-01-00 2013-01-00 PubMed: 23032973 DOI: 10.1038/mt.2012.207Associated cell lines:
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Fatima A, Kaifeng S, Dittmann S, Xu G, Gupta MK, Linke M, Zechner U, Nguemo F, Milting H, Farr M, Hescheler J, Sarić T
The disease-specific phenotype in cardiomyocytes derived from induced pluripotent stem cells of two long QT syndrome type 3 patients
Fatima A et al. The disease-specific phenotype in cardiomyocytes derived from induced pluripotent stem cells of two long QT syndrome type 3 patients. . 2013-00-00. Pubmed ID: 24349418; DOI: 10.1371/journal.pone.0083005; PMC: PMC3859612 UKKi008-AUKKi009-AUKKi009-B 2013-00-00 2013-00-00 PubMed: 24349418 DOI: 10.1371/journal.pone.0083005 -
Lesbros C, Martin V, Najbar W, Sanquer A, McGahie D, Eun HM, Gueguen S
Protective Efficacy of the Calicivirus Valency of the Leucofeligen Vaccine against a Virulent Heterologous Challenge in Kittens
Lesbros C et al. Protective Efficacy of the Calicivirus Valency of the Leucofeligen Vaccine against a Virulent Heterologous Challenge in Kittens. . 2013-00-00. Pubmed ID: 23864986; DOI: 10.1155/2013/232397; PMC: PMC3705951 UNEWi001-AUNEWi004-AUNEWi005-A 2013-00-00 2013-00-00 PubMed: 23864986 DOI: 10.1155/2013/232397Associated cell lines:
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Kreitzer FR, Salomonis N, Sheehan A, Huang M, Park JS, Spindler MJ, Lizarraga P, Weiss WA, So PL, Conklin BR
A robust method to derive functional neural crest cells from human pluripotent stem cells
Kreitzer FR et al. A robust method to derive functional neural crest cells from human pluripotent stem cells. . 2013-00-00. Pubmed ID: 23862100; PMC: PMC3708511 UCSFi001-A 2013-00-00 2013-00-00 PubMed: 23862100Associated cell lines:
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Vuoristo S, Toivonen S, Weltner J, Mikkola M, Ustinov J, Trokovic R, Palgi J, Lund R, Tuuri T, Otonkoski T
A novel feeder-free culture system for human pluripotent stem cell culture and induced pluripotent stem cell derivation
Vuoristo S et al. A novel feeder-free culture system for human pluripotent stem cell culture and induced pluripotent stem cell derivation. . 2013-00-00. Pubmed ID: 24098444; DOI: 10.1371/journal.pone.0076205; PMC: PMC3788803 UHe003-AUHi007-B 2013-00-00 2013-00-00 PubMed: 24098444 DOI: 10.1371/journal.pone.0076205 -
van Wilgenburg B, Browne C, Vowles J, Cowley SA
Efficient, long term production of monocyte-derived macrophages from human pluripotent stem cells under partly-defined and fully-defined conditions
van Wilgenburg B et al. Efficient, long term production of monocyte-derived macrophages from human pluripotent stem cells under partly-defined and fully-defined conditions. . 2013-00-00. Pubmed ID: 23951090; DOI: 10.1371/journal.pone.0071098; PMC: PMC3741356 UOXFi004-AUOXFi004-B 2013-00-00 2013-00-00 PubMed: 23951090 DOI: 10.1371/journal.pone.0071098Associated cell lines:
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Liu GH, Qu J, Suzuki K, Nivet E, Li M, Montserrat N, Yi F, Xu X, Ruiz S, Zhang W, Wagner U, Kim A, Ren B, Li Y, Goebl A, Kim J, Soligalla RD, Dubova I, Thompson J, Yates J 3rd, Esteban CR, Sancho-Martinez I, Izpisua Belmonte JC
Progressive degeneration of human neural stem cells caused by pathogenic LRRK2
Liu GH et al. Progressive degeneration of human neural stem cells caused by pathogenic LRRK2. . 2012-11-22. Pubmed ID: 23075850; DOI: 10.1038/nature11557; PMC: PMC3504651 ESi061-A 2012-11-22 2012-11-22 PubMed: 23075850 DOI: 10.1038/nature11557Associated cell lines:
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Imaizumi Y, Okada Y, Akamatsu W, Koike M, Kuzumaki N, Hayakawa H, Nihira T, Kobayashi T, Ohyama M, Sato S, Takanashi M, Funayama M, Hirayama A, Soga T, Hishiki T, Suematsu M, Yagi T, Ito D, Kosakai A, Hayashi K, Shouji M, Nakanishi A, Suzuki N, Mizuno Y, Mizushima N, Amagai M, Uchiyama Y, Mochizuki H, Hattori N, Okano H
Mitochondrial dysfunction associated with increased oxidative stress and α-synuclein accumulation in PARK2 iPSC-derived neurons and postmortem brain tissue
Imaizumi Y et al. Mitochondrial dysfunction associated with increased oxidative stress and α-synuclein accumulation in PARK2 iPSC-derived neurons and postmortem brain tissue. . 2012-10-06. Pubmed ID: 23039195; DOI: 10.1186/1756-6606-5-35; PMC: PMC3546866 KUIFMSi004-C 2012-10-06 2012-10-06 PubMed: 23039195 DOI: 10.1186/1756-6606-5-35Associated cell lines:
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Zahabi A, Shahbazi E, Ahmadieh H, Hassani SN, Totonchi M, Taei A, Masoudi N, Ebrahimi M, Aghdami N, Seifinejad A, Mehrnejad F, Daftarian N, Salekdeh GH, Baharvand H
A new efficient protocol for directed differentiation of retinal pigmented epithelial cells from normal and retinal disease induced pluripotent stem cells
Zahabi A et al. A new efficient protocol for directed differentiation of retinal pigmented epithelial cells from normal and retinal disease induced pluripotent stem cells. . 2012-08-10. Pubmed ID: 22145677; DOI: 10.1089/scd.2011.0599 RIe006-ARIi009-ARIi010-ARIi011-ARIi012-ARIi014-A 2012-08-10 2012-08-10 PubMed: 22145677 DOI: 10.1089/scd.2011.0599 -
Pruksananonda K, Rungsiwiwut R, Numchaisrika P, Ahnonkitpanit V, Isarasena N, Virutamasen P
Eighteen-year cryopreservation does not negatively affect the pluripotency of human embryos: evidence from embryonic stem cell derivation
Pruksananonda K et al. Eighteen-year cryopreservation does not negatively affect the pluripotency of human embryos: evidence from embryonic stem cell derivation. . 2012-08-00. Pubmed ID: 23514952; DOI: 10.1089/biores.2012.0242; PMC: PMC3559204 CHULAe001-A 2012-08-00 2012-08-00 PubMed: 23514952 DOI: 10.1089/biores.2012.0242Associated cell lines:
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Kajiwara M, Aoi T, Okita K, Takahashi R, Inoue H, Takayama N, Endo H, Eto K, Toguchida J, Uemoto S, Yamanaka S
Donor-dependent variations in hepatic differentiation from human-induced pluripotent stem cells
Kajiwara M et al. Donor-dependent variations in hepatic differentiation from human-induced pluripotent stem cells. . 2012-07-31. Pubmed ID: 22802639; DOI: 10.1073/pnas.1209979109; PMC: PMC3411998 WAe001-AWAe009-AESIBIe003-AESIBIe004-AKUIMSe001-AKUIMSe003-AESIBIe006-AKUIFMSi004-BKUIFMSi004-CCIRAi007-A 2012-07-31 2012-07-31 PubMed: 22802639 DOI: 10.1073/pnas.1209979109Associated cell lines:
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Tedesco FS, Gerli MF, Perani L, Benedetti S, Ungaro F, Cassano M, Antonini S, Tagliafico E, Artusi V, Longa E, Tonlorenzi R, Ragazzi M, Calderazzi G, Hoshiya H, Cappellari O, Mora M, Schoser B, Schneiderat P, Oshimura M, Bottinelli R, Sampaolesi M, Torrente Y, Broccoli V, Cossu G
Transplantation of genetically corrected human iPSC-derived progenitors in mice with limb-girdle muscular dystrophy
Tedesco FS et al. Transplantation of genetically corrected human iPSC-derived progenitors in mice with limb-girdle muscular dystrophy. . 2012-06-27. Pubmed ID: 22745439; DOI: 10.1126/scitranslmed.3003541 UCLi005-A 2012-06-27 2012-06-27 PubMed: 22745439 DOI: 10.1126/scitranslmed.3003541Associated cell lines:
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Ramos-Mejía V, Fernández AF, Ayllón V, Real PJ, Bueno C, Anderson P, Martín F, Fraga MF, Menendez P
Maintenance of human embryonic stem cells in mesenchymal stem cell-conditioned media augments hematopoietic specification
Ramos-Mejía V et al. Maintenance of human embryonic stem cells in mesenchymal stem cell-conditioned media augments hematopoietic specification. . 2012-06-10. Pubmed ID: 21936705; DOI: 10.1089/scd.2011.0400 AXORe002-AWAe009-AWAe013-AESe029-A 2012-06-10 2012-06-10 PubMed: 21936705 DOI: 10.1089/scd.2011.0400Associated cell lines:
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Faradonbeh MZ, Gharechahi J, Mollamohammadi S, Pakzad M, Taei A, Rassouli H, Baharvand H, Salekdeh GH
An orthogonal comparison of the proteome of human embryonic stem cells with that of human induced pluripotent stem cells of different genetic background
Faradonbeh MZ et al. An orthogonal comparison of the proteome of human embryonic stem cells with that of human induced pluripotent stem cells of different genetic background. . 2012-06-00. Pubmed ID: 22543856; DOI: 10.1039/c2mb25018g RIe005-ARIe006-ARIi001-ARIi002-ARIi005-ARIi007-A 2012-06-00 2012-06-00 PubMed: 22543856 DOI: 10.1039/c2mb25018g -
Griscelli F, Féraud O, Oudrhiri N, Gobbo E, Casal I, Chomel JC, Biéche I, Duvillard P, Opolon P, Turhan AG, Bennaceur-Griscelli A
Malignant germ cell-like tumors, expressing Ki-1 antigen (CD30), are revealed during in vivo differentiation of partially reprogrammed human-induced pluripotent stem cells
Griscelli F et al. Malignant germ cell-like tumors, expressing Ki-1 antigen (CD30), are revealed during in vivo differentiation of partially reprogrammed human-induced pluripotent stem cells. . 2012-05-00. Pubmed ID: 22425713; DOI: 10.1016/j.ajpath.2012.01.011 UPSFRi001-AUPSFRi002-AUPSFRi004-AUPSFRi005-AUPSFRi008-AUPSFRi009-AUPSFRi004-A-1 2012-05-00 2012-05-00 PubMed: 22425713 DOI: 10.1016/j.ajpath.2012.01.011Associated cell lines:
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Sánchez-Danés A, Richaud-Patin Y, Carballo-Carbajal I, Jiménez-Delgado S, Caig C, Mora S, Di Guglielmo C, Ezquerra M, Patel B, Giralt A, Canals JM, Memo M, Alberch J, López-Barneo J, Vila M, Cuervo AM, Tolosa E, Consiglio A, Raya A
Disease-specific phenotypes in dopamine neurons from human iPS-based models of genetic and sporadic Parkinson's disease
Sánchez-Danés A et al. Disease-specific phenotypes in dopamine neurons from human iPS-based models of genetic and sporadic Parkinson's disease. . 2012-05-00. Pubmed ID: 22407749; DOI: 10.1002/emmm.201200215; PMC: PMC3403296 ESi001-AESi002-AESi006-AESi081-A 2012-05-00 2012-05-00 PubMed: 22407749 DOI: 10.1002/emmm.201200215 -
Funk WD, Labat I, Sampathkumar J, Gourraud PA, Oksenberg JR, Rosler E, Steiger D, Sheibani N, Caillier S, Stache-Crain B, Johnson JA, Meisner L, Lacher MD, Chapman KB, Park MJ, Shin KJ, Drmanac R, West MD
Evaluating the genomic and sequence integrity of human ES cell lines; comparison to normal genomes
Funk WD et al. Evaluating the genomic and sequence integrity of human ES cell lines; comparison to normal genomes. . 2012-03-00. Pubmed ID: 22265736; DOI: 10.1016/j.scr.2011.10.001 SSCCe003-ASSCCe004-ASSCCe005-ASSCCe007-ASSCCe008-A 2012-03-00 2012-03-00 PubMed: 22265736 DOI: 10.1016/j.scr.2011.10.001Associated cell lines:
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Brøchner CB, Johansen JS, Larsen LA, Bak M, Mikkelsen HB, Byskov AG, Andersen CY, Møllgård K
YKL-40 is differentially expressed in human embryonic stem cells and in cell progeny of the three germ layers
Brøchner CB et al. YKL-40 is differentially expressed in human embryonic stem cells and in cell progeny of the three germ layers. . 2012-03-00. Pubmed ID: 22140133; DOI: 10.1369/0022155411433331; PMC: PMC3351129 KUe001-AKUe002-AKUe003-AKUe013-AKUe014-A 2012-03-00 2012-03-00 PubMed: 22140133 DOI: 10.1369/0022155411433331 -
Jung CB, Moretti A, Mederos y Schnitzler M, Iop L, Storch U, Bellin M, Dorn T, Ruppenthal S, Pfeiffer S, Goedel A, Dirschinger RJ, Seyfarth M, Lam JT, Sinnecker D, Gudermann T, Lipp P, Laugwitz KL
Dantrolene rescues arrhythmogenic RYR2 defect in a patient-specific stem cell model of catecholaminergic polymorphic ventricular tachycardia
Jung CB et al. Dantrolene rescues arrhythmogenic RYR2 defect in a patient-specific stem cell model of catecholaminergic polymorphic ventricular tachycardia. . 2012-03-00. Pubmed ID: 22174035; DOI: 10.1002/emmm.201100194; PMC: PMC3376852 MRIi007-A 2012-03-00 2012-03-00 PubMed: 22174035 DOI: 10.1002/emmm.201100194Associated cell lines:
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Kunisada Y, Tsubooka-Yamazoe N, Shoji M, Hosoya M
Small molecules induce efficient differentiation into insulin-producing cells from human induced pluripotent stem cells
Kunisada Y et al. Small molecules induce efficient differentiation into insulin-producing cells from human induced pluripotent stem cells. . 2012-03-00. Pubmed ID: 22056147; DOI: 10.1016/j.scr.2011.10.002 KUIFMSi004-C 2012-03-00 2012-03-00 PubMed: 22056147 DOI: 10.1016/j.scr.2011.10.002Associated cell lines:
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Lahti AL, Kujala VJ, Chapman H, Koivisto AP, Pekkanen-Mattila M, Kerkelä E, Hyttinen J, Kontula K, Swan H, Conklin BR, Yamanaka S, Silvennoinen O, Aalto-Setälä K
Model for long QT syndrome type 2 using human iPS cells demonstrates arrhythmogenic characteristics in cell culture
Lahti AL et al. Model for long QT syndrome type 2 using human iPS cells demonstrates arrhythmogenic characteristics in cell culture. . 2012-03-00. Pubmed ID: 22052944; DOI: 10.1242/dmm.008409; PMC: PMC3291643 TAUi002-A 2012-03-00 2012-03-00 PubMed: 22052944 DOI: 10.1242/dmm.008409Associated cell lines:
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Yagi T, Ito D, Okada Y, Akamatsu W, Nihei Y, Yoshizaki T, Yamanaka S, Okano H, Suzuki N
Modeling familial Alzheimer's disease with induced pluripotent stem cells
Yagi T et al. Modeling familial Alzheimer's disease with induced pluripotent stem cells. . 2011-12-01. Pubmed ID: 21900357; DOI: 10.1093/hmg/ddr394 KUIFMSi004-C 2011-12-01 2011-12-01 PubMed: 21900357 DOI: 10.1093/hmg/ddr394Associated cell lines:
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Kujala K, Paavola J, Lahti A, Larsson K, Pekkanen-Mattila M, Viitasalo M, Lahtinen AM, Toivonen L, Kontula K, Swan H, Laine M, Silvennoinen O, Aalto-Setälä K
Cell model of catecholaminergic polymorphic ventricular tachycardia reveals early and delayed afterdepolarizations
Kujala K et al. Cell model of catecholaminergic polymorphic ventricular tachycardia reveals early and delayed afterdepolarizations. . 2012-00-00. Pubmed ID: 22962621; DOI: 10.1371/journal.pone.0044660; PMC: PMC3433449 TAUi002-ATAUi004-A 2012-00-00 2012-00-00 PubMed: 22962621 DOI: 10.1371/journal.pone.0044660 -
Schulz TC, Young HY, Agulnick AD, Babin MJ, Baetge EE, Bang AG, Bhoumik A, Cepa I, Cesario RM, Haakmeester C, Kadoya K, Kelly JR, Kerr J, Martinson LA, McLean AB, Moorman MA, Payne JK, Richardson M, Ross KG, Sherrer ES, Song X, Wilson AZ, Brandon EP, Green CE, Kroon EJ, Kelly OG, D'Amour KA, Robins AJ
A scalable system for production of functional pancreatic progenitors from human embryonic stem cells
Schulz TC et al. A scalable system for production of functional pancreatic progenitors from human embryonic stem cells. . 2012-00-00. Pubmed ID: 22623968; DOI: 10.1371/journal.pone.0037004; PMC: PMC3356395 VCYTe001-A 2012-00-00 2012-00-00 PubMed: 22623968 DOI: 10.1371/journal.pone.0037004Associated cell lines:
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Tannenbaum SE, Turetsky TT, Singer O, Aizenman E, Kirshberg S, Ilouz N, Gil Y, Berman-Zaken Y, Perlman TS, Geva N, Levy O, Arbell D, Simon A, Ben-Meir A, Shufaro Y, Laufer N, Reubinoff BE
Derivation of xeno-free and GMP-grade human embryonic stem cells--platforms for future clinical applications
Tannenbaum SE et al. Derivation of xeno-free and GMP-grade human embryonic stem cells--platforms for future clinical applications. . 2012-00-00. Pubmed ID: 22745653; DOI: 10.1371/journal.pone.0035325; PMC: PMC3380026 HADe007-AHADe008-AHADe009-AHADe012-AHADe013-AHADe007-BHADe008-BHADe009-BHADe007-C 2012-00-00 2012-00-00 PubMed: 22745653 DOI: 10.1371/journal.pone.0035325 -
Sandt C, Féraud O, Oudrhiri N, Bonnet ML, Meunier MC, Valogne Y, Bertrand A, Raphaël M, Griscelli F, Turhan AG, Dumas P, Bennaceur-Griscelli A
Identification of spectral modifications occurring during reprogramming of somatic cells
Sandt C et al. Identification of spectral modifications occurring during reprogramming of somatic cells. . 2012-00-00. Pubmed ID: 22514597; DOI: 10.1371/journal.pone.0030743; PMC: PMC3326006 HVRDe003-AWAe001-AWAe009-AUPSFRe001-AUPSFRe002-AUPSFRe003-AUPSFRi001-AUPSFRi002-AUPSFRi007-AUPSFRi008-AUPSFRi009-A 2012-00-00 2012-00-00 PubMed: 22514597 DOI: 10.1371/journal.pone.0030743Associated cell lines:
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Park TS, Huo JS, Peters A, Talbot CC Jr, Verma K, Zimmerlin L, Kaplan IM, Zambidis ET
Growth factor-activated stem cell circuits and stromal signals cooperatively accelerate non-integrated iPSC reprogramming of human myeloid progenitors
Park TS et al. Growth factor-activated stem cell circuits and stromal signals cooperatively accelerate non-integrated iPSC reprogramming of human myeloid progenitors. . 2012-00-00. Pubmed ID: 22905176; DOI: 10.1371/journal.pone.0042838; PMC: PMC3414503 WISCi004-AWISCi004-BTMOi001-A 2012-00-00 2012-00-00 PubMed: 22905176 DOI: 10.1371/journal.pone.0042838Associated cell lines:
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Ojala M, Rajala K, Pekkanen-Mattila M, Miettinen M, Huhtala H, Aalto-Setälä K
Culture conditions affect cardiac differentiation potential of human pluripotent stem cells
Ojala M et al. Culture conditions affect cardiac differentiation potential of human pluripotent stem cells. . 2012-00-00. Pubmed ID: 23119085; DOI: 10.1371/journal.pone.0048659; PMC: PMC3485380 TAUi002-A 2012-00-00 2012-00-00 PubMed: 23119085 DOI: 10.1371/journal.pone.0048659Associated cell lines:
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Pekkanen-Mattila M, Ojala M, Kerkelä E, Rajala K, Skottman H, Aalto-Setälä K
The effect of human and mouse fibroblast feeder cells on cardiac differentiation of human pluripotent stem cells
Pekkanen-Mattila M et al. The effect of human and mouse fibroblast feeder cells on cardiac differentiation of human pluripotent stem cells. . 2012-00-00. Pubmed ID: 22315618; DOI: 10.1155/2012/875059; PMC: PMC3270482 WAe007-AUTAe006-A 2012-00-00 2012-00-00 PubMed: 22315618 DOI: 10.1155/2012/875059 -
Yagi T, Kosakai A, Ito D, Okada Y, Akamatsu W, Nihei Y, Nabetani A, Ishikawa F, Arai Y, Hirose N, Okano H, Suzuki N
Establishment of induced pluripotent stem cells from centenarians for neurodegenerative disease research
Yagi T et al. Establishment of induced pluripotent stem cells from centenarians for neurodegenerative disease research. . 2012-00-00. Pubmed ID: 22848530; DOI: 10.1371/journal.pone.0041572; PMC: PMC3405135 KUIFMSi004-C 2012-00-00 2012-00-00 PubMed: 22848530 DOI: 10.1371/journal.pone.0041572Associated cell lines:
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Koch P, Breuer P, Peitz M, Jungverdorben J, Kesavan J, Poppe D, Doerr J, Ladewig J, Mertens J, Tüting T, Hoffmann P, Klockgether T, Evert BO, Wüllner U, Brüstle O
Excitation-induced ataxin-3 aggregation in neurons from patients with Machado-Joseph disease
Koch P et al. Excitation-induced ataxin-3 aggregation in neurons from patients with Machado-Joseph disease. . 2011-11-23. Pubmed ID: 22113611; DOI: 10.1038/nature10671 UKBi002-AUKBi003-AUKBi004-AUKBi007-AUKBi008-AUKBi001-B 2011-11-23 2011-11-23 PubMed: 22113611 DOI: 10.1038/nature10671 -
Munoz J, Low TY, Kok YJ, Chin A, Frese CK, Ding V, Choo A, Heck AJ
The quantitative proteomes of human-induced pluripotent stem cells and embryonic stem cells
Munoz J et al. The quantitative proteomes of human-induced pluripotent stem cells and embryonic stem cells. . 2011-11-22. Pubmed ID: 22108792; DOI: 10.1038/msb.2011.84; PMC: PMC3261715 ESIBIe003-A 2011-11-22 2011-11-22 PubMed: 22108792 DOI: 10.1038/msb.2011.84Associated cell lines:
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Greber B, Coulon P, Zhang M, Moritz S, Frank S, Müller-Molina AJ, Araúzo-Bravo MJ, Han DW, Pape HC, Schöler HR
FGF signalling inhibits neural induction in human embryonic stem cells
Greber B et al. FGF signalling inhibits neural induction in human embryonic stem cells. . 2011-11-15. Pubmed ID: 22085933; DOI: 10.1038/emboj.2011.407; PMC: PMC3243624 HVRDe006-AUNEWe003-A 2011-11-15 2011-11-15 PubMed: 22085933 DOI: 10.1038/emboj.2011.407Associated cell lines:
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Larijani MR, Seifinejad A, Pournasr B, Hajihoseini V, Hassani SN, Totonchi M, Yousefi M, Shamsi F, Salekdeh GH, Baharvand H
Long-term maintenance of undifferentiated human embryonic and induced pluripotent stem cells in suspension
Larijani MR et al. Long-term maintenance of undifferentiated human embryonic and induced pluripotent stem cells in suspension. . 2011-11-00. Pubmed ID: 21198400; DOI: 10.1089/scd.2010.0517 RIe005-ARIe006-ARIi001-ARIi007-A 2011-11-00 2011-11-00 PubMed: 21198400 DOI: 10.1089/scd.2010.0517 -
Yusa K, Rashid ST, Strick-Marchand H, Varela I, Liu PQ, Paschon DE, Miranda E, Ordóñez A, Hannan NR, Rouhani FJ, Darche S, Alexander G, Marciniak SJ, Fusaki N, Hasegawa M, Holmes MC, Di Santo JP, Lomas DA, Bradley A, Vallier L
Targeted gene correction of α1-antitrypsin deficiency in induced pluripotent stem cells
Yusa K et al. Targeted gene correction of α1-antitrypsin deficiency in induced pluripotent stem cells. . 2011-10-12. Pubmed ID: 21993621; DOI: 10.1038/nature10424; PMC: PMC3198846 CAMi014-A 2011-10-12 2011-10-12 PubMed: 21993621 DOI: 10.1038/nature10424Associated cell lines:
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Nihat Zafer, Kahram Semra
Derivation and Characterization of New hESC Lines from Supernumerary Embryos, Experience from Turkey
Nihat Zafer et al. Derivation and Characterization of New hESC Lines from Supernumerary Embryos, Experience from Turkey. . 2011-09-15. DOI: 10.5772/25010 IMHe001-AIMHe002-AIMHe003-AIMHe004-AIMHe005-AIMHe006-AIMHe007-AIMHe008-AIMHe009-AIMHe010-AIMHe011-AIMHe012-AIMHe013-AIMHe014-AIMHe015-AIMHe016-AIMHe017-AIMHe018-A 2011-09-15 2011-09-15 DOI: 10.5772/25010 -
Phanstiel DH, Brumbaugh J, Wenger CD, Tian S, Probasco MD, Bailey DJ, Swaney DL, Tervo MA, Bolin JM, Ruotti V, Stewart R, Thomson JA, Coon JJ
Proteomic and phosphoproteomic comparison of human ES and iPS cells
Phanstiel DH et al. Proteomic and phosphoproteomic comparison of human ES and iPS cells. . 2011-09-11. Pubmed ID: 21983960; DOI: 10.1038/nmeth.1699; PMC: PMC3432645 WAe001-AWAe007-AWAe009-AWAe014-AWAi001-AWAi001-BWAi001-C 2011-09-11 2011-09-11 PubMed: 21983960 DOI: 10.1038/nmeth.1699 -
Ma YL, Zhang P, Wang F, Moyer MP, Yang JJ, Liu ZH, Peng JY, Chen HQ, Zhou YK, Liu WJ, Qin HL
Human embryonic stem cells and metastatic colorectal cancer cells shared the common endogenous human microRNA-26b
Ma YL et al. Human embryonic stem cells and metastatic colorectal cancer cells shared the common endogenous human microRNA-26b. . 2011-09-00. Pubmed ID: 20831567; DOI: 10.1111/j.1582-4934.2010.01170.x; PMC: PMC3918049 HVRDe017-A 2011-09-00 2011-09-00 PubMed: 20831567 DOI: 10.1111/j.1582-4934.2010.01170.xAssociated cell lines:
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Lee JY, Lee DY, Choi YS, Lee KJ, Kim YO
Registration of human embryonic stem cell lines: Korea, 2010
Lee JY et al. Registration of human embryonic stem cell lines: Korea, 2010. . 2011-09-00. Pubmed ID: 24159464; DOI: 10.1016/j.phrp.2011.07.002; PMC: PMC3766916 SNUe001-ASNUe002-ASNUe003-ACHAe001-AMIZMe007-ASNUe004-ASNUe005-ASNUe006-ACHAe002-ASNUe007-A 2011-09-00 2011-09-00 PubMed: 24159464 DOI: 10.1016/j.phrp.2011.07.002 -
Ramirez JM, Gerbal-Chaloin S, Milhavet O, Qiang B, Becker F, Assou S, Lemaître JM, Hamamah S, De Vos J
Brief report: benchmarking human pluripotent stem cell markers during differentiation into the three germ layers unveils a striking heterogeneity: all markers are not equal
Ramirez JM et al. Brief report: benchmarking human pluripotent stem cell markers during differentiation into the three germ layers unveils a striking heterogeneity: all markers are not equal. . 2011-09-00. Pubmed ID: 21714037; DOI: 10.1002/stem.681 HVRDe001-AWAe001-A 2011-09-00 2011-09-00 PubMed: 21714037 DOI: 10.1002/stem.681Associated cell lines:
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Devine MJ, Ryten M, Vodicka P, Thomson AJ, Burdon T, Houlden H, Cavaleri F, Nagano M, Drummond NJ, Taanman JW, Schapira AH, Gwinn K, Hardy J, Lewis PA, Kunath T
Parkinson's disease induced pluripotent stem cells with triplication of the α-synuclein locus
Devine MJ et al. Parkinson's disease induced pluripotent stem cells with triplication of the α-synuclein locus. . 2011-08-23. Pubmed ID: 21863007; DOI: 10.1038/ncomms1453; PMC: PMC3265381 EDi001-AEDi001-A-1EDi002-AEDi001-BEDi001-B-1EDi001-B-2EDi001-B-3EDi001-B-4 2011-08-23 2011-08-23 PubMed: 21863007 DOI: 10.1038/ncomms1453Associated cell lines:
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Zhou T, Benda C, Duzinger S, Huang Y, Li X, Li Y, Guo X, Cao G, Chen S, Hao L, Chan YC, Ng KM, Ho JC, Wieser M, Wu J, Redl H, Tse HF, Grillari J, Grillari-Voglauer R, Pei D, Esteban MA
Generation of induced pluripotent stem cells from urine
Zhou T et al. Generation of induced pluripotent stem cells from urine. . 2011-07-00. Pubmed ID: 21636641; DOI: 10.1681/asn.2011010106; PMC: PMC3137570 GIBHi002-A 2011-07-00 2011-07-00 PubMed: 21636641 DOI: 10.1681/asn.2011010106Associated cell lines:
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Treff NR, Su J, Tao X, Northrop LE, Scott RT Jr
Single-cell whole-genome amplification technique impacts the accuracy of SNP microarray-based genotyping and copy number analyses
Treff NR et al. Single-cell whole-genome amplification technique impacts the accuracy of SNP microarray-based genotyping and copy number analyses. . 2011-06-00. Pubmed ID: 21177337; DOI: 10.1093/molehr/gaq103; PMC: PMC3097071 KAUSTi003-AKAUSTi004-AKAUSTi004-BKAUSTi005-AKAUSTi005-BKAUSTi005-C 2011-06-00 2011-06-00 PubMed: 21177337 DOI: 10.1093/molehr/gaq103Associated cell lines:
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Nagvenkar P, Pethe P, Pawani H, Telang J, Kumar N, Hinduja I, Zaveri K, Bhartiya D
Evaluating differentiation propensity of in-house derived human embryonic stem cell lines KIND-1 and KIND-2
Nagvenkar P et al. Evaluating differentiation propensity of in-house derived human embryonic stem cell lines KIND-1 and KIND-2. . 2011-06-00. Pubmed ID: 21614653; DOI: 10.1007/s11626-011-9420-9 NIRRHe001-ANIRRHe002-A 2011-06-00 2011-06-00 PubMed: 21614653 DOI: 10.1007/s11626-011-9420-9Associated cell lines:
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Nishino K, Toyoda M, Yamazaki-Inoue M, Fukawatase Y, Chikazawa E, Sakaguchi H, Akutsu H, Umezawa A
DNA methylation dynamics in human induced pluripotent stem cells over time
Nishino K et al. DNA methylation dynamics in human induced pluripotent stem cells over time. . 2011-05-00. Pubmed ID: 21637780; DOI: 10.1371/journal.pgen.1002085; PMC: PMC3102737 HVRDe002-AHVRDe003-AHVRDe006-AHVRDe008-AHVRDe009-AKUIFMSi004-C 2011-05-00 2011-05-00 PubMed: 21637780 DOI: 10.1371/journal.pgen.1002085Associated cell lines:
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Okita K, Matsumura Y, Sato Y, Okada A, Morizane A, Okamoto S, Hong H, Nakagawa M, Tanabe K, Tezuka K, Shibata T, Kunisada T, Takahashi M, Takahashi J, Saji H, Yamanaka S
A more efficient method to generate integration-free human iPS cells
Okita K et al. A more efficient method to generate integration-free human iPS cells. . 2011-05-00. Pubmed ID: 21460823; DOI: 10.1038/nmeth.1591 KUIMSe001-AKUIMSe003-AKUIFMSi004-CCIRAi007-AKUIMSi004-F 2011-05-00 2011-05-00 PubMed: 21460823 DOI: 10.1038/nmeth.1591Associated cell lines:
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Chen G, Gulbranson DR, Hou Z, Bolin JM, Ruotti V, Probasco MD, Smuga-Otto K, Howden SE, Diol NR, Propson NE, Wagner R, Lee GO, Antosiewicz-Bourget J, Teng JM, Thomson JA
Chemically defined conditions for human iPSC derivation and culture
Chen G et al. Chemically defined conditions for human iPSC derivation and culture. . 2011-05-00. Pubmed ID: 21478862; DOI: 10.1038/nmeth.1593; PMC: PMC3084903 NHLBIi003-A 2011-05-00 2011-05-00 PubMed: 21478862 DOI: 10.1038/nmeth.1593Associated cell lines:
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Burridge PW, Thompson S, Millrod MA, Weinberg S, Yuan X, Peters A, Mahairaki V, Koliatsos VE, Tung L, Zambidis ET
A universal system for highly efficient cardiac differentiation of human induced pluripotent stem cells that eliminates interline variability
Burridge PW et al. A universal system for highly efficient cardiac differentiation of human induced pluripotent stem cells that eliminates interline variability. . 2011-04-08. Pubmed ID: 21494607; DOI: 10.1371/journal.pone.0018293; PMC: PMC3072973 TMOi001-ATMOi001-A-1 2011-04-08 2011-04-08 PubMed: 21494607 DOI: 10.1371/journal.pone.0018293Associated cell lines:
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Hu K, Yu J, Suknuntha K, Tian S, Montgomery K, Choi KD, Stewart R, Thomson JA, Slukvin II
Efficient generation of transgene-free induced pluripotent stem cells from normal and neoplastic bone marrow and cord blood mononuclear cells
Hu K et al. Efficient generation of transgene-free induced pluripotent stem cells from normal and neoplastic bone marrow and cord blood mononuclear cells. . 2011-04-07. Pubmed ID: 21296996; DOI: 10.1182/blood-2010-07-298331; PMC: PMC3083304 WAi001-AWAi001-BWAi001-C 2011-04-07 2011-04-07 PubMed: 21296996 DOI: 10.1182/blood-2010-07-298331 -
Rigbolt KT, Prokhorova TA, Akimov V, Henningsen J, Johansen PT, Kratchmarova I, Kassem M, Mann M, Olsen JV, Blagoev B
System-wide temporal characterization of the proteome and phosphoproteome of human embryonic stem cell differentiation
Rigbolt KT et al. System-wide temporal characterization of the proteome and phosphoproteome of human embryonic stem cell differentiation. . 2011-03-15. Pubmed ID: 21406692; DOI: 10.1126/scisignal.2001570 HVRDe009-A 2011-03-15 2011-03-15 PubMed: 21406692 DOI: 10.1126/scisignal.2001570Associated cell lines:
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Gore A, Li Z, Fung HL, Young JE, Agarwal S, Antosiewicz-Bourget J, Canto I, Giorgetti A, Israel MA, Kiskinis E, Lee JH, Loh YH, Manos PD, Montserrat N, Panopoulos AD, Ruiz S, Wilbert ML, Yu J, Kirkness EF, Izpisua Belmonte JC, Rossi DJ, Thomson JA, Eggan K, Daley GQ, Goldstein LS, Zhang K
Somatic coding mutations in human induced pluripotent stem cells
Gore A et al. Somatic coding mutations in human induced pluripotent stem cells. . 2011-03-03. Pubmed ID: 21368825; DOI: 10.1038/nature09805; PMC: PMC3074107 HVRDi009-A 2011-03-03 2011-03-03 PubMed: 21368825 DOI: 10.1038/nature09805Associated cell lines:
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Boulting GL, Kiskinis E, Croft GF, Amoroso MW, Oakley DH, Wainger BJ, Williams DJ, Kahler DJ, Yamaki M, Davidow L, Rodolfa CT, Dimos JT, Mikkilineni S, MacDermott AB, Woolf CJ, Henderson CE, Wichterle H, Eggan K
A functionally characterized test set of human induced pluripotent stem cells
Boulting GL et al. A functionally characterized test set of human induced pluripotent stem cells. . 2011-03-00. Pubmed ID: 21293464; DOI: 10.1038/nbt.1783; PMC: PMC3229307 HVRDi006-AHVRDi008-AHVRDi009-AHVRDi008-BHVRDi009-B 2011-03-00 2011-03-00 PubMed: 21293464 DOI: 10.1038/nbt.1783Associated cell lines:
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Bradley CK, Scott HA, Chami O, Peura TT, Dumevska B, Schmidt U, Stojanov T
Derivation of Huntington's disease-affected human embryonic stem cell lines
Bradley CK et al. Derivation of Huntington's disease-affected human embryonic stem cell lines. . 2011-03-00. Pubmed ID: 20649476; DOI: 10.1089/scd.2010.0120 GENEAe015-AGENEAe020-A 2011-03-00 2011-03-00 PubMed: 20649476 DOI: 10.1089/scd.2010.0120Associated cell lines:
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Bock C, Kiskinis E, Verstappen G, Gu H, Boulting G, Smith ZD, Ziller M, Croft GF, Amoroso MW, Oakley DH, Gnirke A, Eggan K, Meissner A
Reference Maps of human ES and iPS cell variation enable high-throughput characterization of pluripotent cell lines
Bock C et al. Reference Maps of human ES and iPS cell variation enable high-throughput characterization of pluripotent cell lines. . 2011-02-04. Pubmed ID: 21295703; DOI: 10.1016/j.cell.2010.12.032; PMC: PMC3063454 HVRDe001-AHVRDe003-AHVRDe006-AHVRDe008-AHVRDe009-AHVRDe013-AWAe001-AWAe007-AWAe009-AHVRDi006-AHVRDi008-AHVRDi008-B 2011-02-04 2011-02-04 PubMed: 21295703 DOI: 10.1016/j.cell.2010.12.032Associated cell lines:
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Ohta S, Imaizumi Y, Okada Y, Akamatsu W, Kuwahara R, Ohyama M, Amagai M, Matsuzaki Y, Yamanaka S, Okano H, Kawakami Y
Generation of human melanocytes from induced pluripotent stem cells
Ohta S et al. Generation of human melanocytes from induced pluripotent stem cells. . 2011-01-13. Pubmed ID: 21249204; DOI: 10.1371/journal.pone.0016182; PMC: PMC3020956 WAe029-A 2011-01-13 2011-01-13 PubMed: 21249204 DOI: 10.1371/journal.pone.0016182Associated cell lines:
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Ström S, Rodriguez-Wallberg K, Holm F, Bergström R, Eklund L, Strömberg AM, Hovatta O
No relationship between embryo morphology and successful derivation of human embryonic stem cell lines
Ström S et al. No relationship between embryo morphology and successful derivation of human embryonic stem cell lines. . 2010-12-31. Pubmed ID: 21217828; DOI: 10.1371/journal.pone.0015329; PMC: PMC3013107 KIe001-AKIe002-AKIe003-AKIe004-AKIe005-AKIe006-AKIe007-AKIe008-AKIe009-AKIe010-AKIe011-AKIe012-AKIe013-AKIe014-AKIe015-AKIe016-AKIe017-AKIe018-AKIe019-AKIe020-AKIe021-AKIe022-AKIe023-AKIe024-AKIe025-AKIe026-AKIe027-AKIe028-AKIe029-AKIe031-A 2010-12-31 2010-12-31 PubMed: 21217828 DOI: 10.1371/journal.pone.0015329 -
Takayama N, Nishimura S, Nakamura S, Shimizu T, Ohnishi R, Endo H, Yamaguchi T, Otsu M, Nishimura K, Nakanishi M, Sawaguchi A, Nagai R, Takahashi K, Yamanaka S, Nakauchi H, Eto K
Transient activation of c-MYC expression is critical for efficient platelet generation from human induced pluripotent stem cells
Takayama N et al. Transient activation of c-MYC expression is critical for efficient platelet generation from human induced pluripotent stem cells. . 2010-12-20. Pubmed ID: 21098095; DOI: 10.1084/jem.20100844; PMC: PMC3005234 KUIMSe003-AKUIFMSi004-BKUIFMSi004-C 2010-12-20 2010-12-20 PubMed: 21098095 DOI: 10.1084/jem.20100844Associated cell lines:
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Fraga AM, Sukoyan M, Rajan P, Braga DP, Iaconelli A Jr, Franco JG Jr, Borges E Jr, Pereira LV
Establishment of a Brazilian line of human embryonic stem cells in defined medium: implications for cell therapy in an ethnically diverse population
Fraga AM et al. Establishment of a Brazilian line of human embryonic stem cells in defined medium: implications for cell therapy in an ethnically diverse population. . 2011-00-00. Pubmed ID: 20719082; DOI: 10.3727/096368910x522261 USPe001-A 2011-00-00 2011-00-00 PubMed: 20719082 DOI: 10.3727/096368910x522261Associated cell lines:
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Fatima A, Xu G, Shao K, Papadopoulos S, Lehmann M, Arnáiz-Cot JJ, Rosa AO, Nguemo F, Matzkies M, Dittmann S, Stone SL, Linke M, Zechner U, Beyer V, Hennies HC, Rosenkranz S, Klauke B, Parwani AS, Haverkamp W, Pfitzer G, Farr M, Cleemann L, Morad M, Milting H, Hescheler J, Saric T
In vitro modeling of ryanodine receptor 2 dysfunction using human induced pluripotent stem cells
Fatima A et al. In vitro modeling of ryanodine receptor 2 dysfunction using human induced pluripotent stem cells. . 2011-00-00. Pubmed ID: 22178870; DOI: 10.1159/000335753; PMC: PMC3709175 UKKi007-AUKKi007-B 2011-00-00 2011-00-00 PubMed: 22178870 DOI: 10.1159/000335753 -
Ghodsizadeh A, Taei A, Totonchi M, Seifinejad A, Gourabi H, Pournasr B, Aghdami N, Malekzadeh R, Almadani N, Salekdeh GH, Baharvand H
Generation of liver disease-specific induced pluripotent stem cells along with efficient differentiation to functional hepatocyte-like cells
Ghodsizadeh A et al. Generation of liver disease-specific induced pluripotent stem cells along with efficient differentiation to functional hepatocyte-like cells. . 2010-12-00. Pubmed ID: 20821352; DOI: 10.1007/s12015-010-9189-3 RIi004-ARIi005-ARIi006-ARIi015-ARIi016-A 2010-12-00 2010-12-00 PubMed: 20821352 DOI: 10.1007/s12015-010-9189-3 -
Byers B, Cord B, Nguyen HN, Schüle B, Fenno L, Lee PC, Deisseroth K, Langston JW, Pera RR, Palmer TD
SNCA triplication Parkinson's patient's iPSC-derived DA neurons accumulate α-synuclein and are susceptible to oxidative stress
Byers B et al. SNCA triplication Parkinson's patient's iPSC-derived DA neurons accumulate α-synuclein and are susceptible to oxidative stress. . 2011-00-00. Pubmed ID: 22110584; DOI: 10.1371/journal.pone.0026159; PMC: PMC3217921 SUSMi005-A 2011-00-00 2011-00-00 PubMed: 22110584 DOI: 10.1371/journal.pone.0026159Associated cell lines:
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Ramos-Mejia V, Melen GJ, Sanchez L, Gutierrez-Aranda I, Ligero G, Cortes JL, Real PJ, Bueno C, Menendez P
Nodal/Activin signaling predicts human pluripotent stem cell lines prone to differentiate toward the hematopoietic lineage
Ramos-Mejia V et al. Nodal/Activin signaling predicts human pluripotent stem cell lines prone to differentiate toward the hematopoietic lineage. . 2010-12-00. Pubmed ID: 20736931; DOI: 10.1038/mt.2010.179; PMC: PMC2997587 KIe001-AESe009-AESe011-AESe013-AAXORe001-AAXORe002-AUOSe003-AWAe001-AWAe009-AWAe013-AESe029-A 2010-12-00 2010-12-00 PubMed: 20736931 DOI: 10.1038/mt.2010.179 -
Moretti A, Bellin M, Welling A, Jung CB, Lam JT, Bott-Flügel L, Dorn T, Goedel A, Höhnke C, Hofmann F, Seyfarth M, Sinnecker D, Schömig A, Laugwitz KL
Patient-specific induced pluripotent stem-cell models for long-QT syndrome
Moretti A et al. Patient-specific induced pluripotent stem-cell models for long-QT syndrome. . 2010-10-07. Pubmed ID: 20660394; DOI: 10.1056/nejmoa0908679 TUMi001-AMRIi005-A 2010-10-07 2010-10-07 PubMed: 20660394 DOI: 10.1056/nejmoa0908679 -
FAN Y, LUO Y, CHEN X, SUN X
A modified culture medium increases blastocyst formation and the efficiency of human embryonic stem cell derivation from poor-quality embryos
FAN Y et al. A modified culture medium increases blastocyst formation and the efficiency of human embryonic stem cell derivation from poor-quality embryos. . 2010-10-00. Pubmed ID: 20657158; DOI: 10.1262/jrd.09-225m GZHMCe002-AGZHMCe003-AGZHMCe004-A 2010-10-00 2010-10-00 PubMed: 20657158 DOI: 10.1262/jrd.09-225mAssociated cell lines:
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Gutierrez-Aranda I, Ramos-Mejia V, Bueno C, Munoz-Lopez M, Real PJ, Mácia A, Sanchez L, Ligero G, Garcia-Parez JL, Menendez P
Human induced pluripotent stem cells develop teratoma more efficiently and faster than human embryonic stem cells regardless the site of injection
Gutierrez-Aranda I et al. Human induced pluripotent stem cells develop teratoma more efficiently and faster than human embryonic stem cells regardless the site of injection. . 2010-09-00. Pubmed ID: 20641038; DOI: 10.1002/stem.471; PMC: PMC2996086 KIe001-AWAe001-AWAe009-AESe029-A 2010-09-00 2010-09-00 PubMed: 20641038 DOI: 10.1002/stem.471 -
Si-Tayeb K, Noto FK, Sepac A, Sedlic F, Bosnjak ZJ, Lough JW, Duncan SA
Generation of human induced pluripotent stem cells by simple transient transfection of plasmid DNA encoding reprogramming factors
Si-Tayeb K et al. Generation of human induced pluripotent stem cells by simple transient transfection of plasmid DNA encoding reprogramming factors. . 2010-08-03. Pubmed ID: 20682060; DOI: 10.1186/1471-213x-10-81; PMC: PMC2923111 MUSCSDi001-A 2010-08-03 2010-08-03 PubMed: 20682060 DOI: 10.1186/1471-213x-10-81Associated cell lines:
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Pryzhkova MV, Peters A, Zambidis ET
Erythropoietic differentiation of a human embryonic stem cell line harbouring the sickle cell anaemia mutation
Pryzhkova MV et al. Erythropoietic differentiation of a human embryonic stem cell line harbouring the sickle cell anaemia mutation. . 2010-08-00. Pubmed ID: 20541472; DOI: 10.1016/j.rbmo.2010.04.017; PMC: PMC3507446 RGIe133-A 2010-08-00 2010-08-00 PubMed: 20541472 DOI: 10.1016/j.rbmo.2010.04.017Associated cell lines:
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Wu R, Xu C, Jin F, Tan Z, Gu B, Chen L, Yao X, Zhang M
Derivation, characterization and differentiation of a new human embryonic stem cell line from a Chinese hatched blastocyst assisted by a non-contact laser system
Wu R et al. Derivation, characterization and differentiation of a new human embryonic stem cell line from a Chinese hatched blastocyst assisted by a non-contact laser system. . 2010-08-00. Pubmed ID: 20973834; DOI: 10.1111/j.1749-0774.2010.00090.x HVRDe003-A 2010-08-00 2010-08-00 PubMed: 20973834 DOI: 10.1111/j.1749-0774.2010.00090.xAssociated cell lines:
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Nilbratt M, Porras O, Marutle A, Hovatta O, Nordberg A
Neurotrophic factors promote cholinergic differentiation in human embryonic stem cell-derived neurons
Nilbratt M et al. Neurotrophic factors promote cholinergic differentiation in human embryonic stem cell-derived neurons. . 2010-06-00. Pubmed ID: 19799651; DOI: 10.1111/j.1582-4934.2009.00916.x; PMC: PMC3829014 KIe007-AKIe009-A 2010-06-00 2010-06-00 PubMed: 19799651 DOI: 10.1111/j.1582-4934.2009.00916.x -
Lengner CJ, Gimelbrant AA, Erwin JA, Cheng AW, Guenther MG, Welstead GG, Alagappan R, Frampton GM, Xu P, Muffat J, Santagata S, Powers D, Barrett CB, Young RA, Lee JT, Jaenisch R, Mitalipova M
Derivation of pre-X inactivation human embryonic stem cells under physiological oxygen concentrations
Lengner CJ et al. Derivation of pre-X inactivation human embryonic stem cells under physiological oxygen concentrations. . 2010-05-28. Pubmed ID: 20471072; DOI: 10.1016/j.cell.2010.04.010 WIBRe001-AWIBRe002-AWIBRe003-AWIBRe001-A-1WIBRe001-A-2 2010-05-28 2010-05-28 PubMed: 20471072 DOI: 10.1016/j.cell.2010.04.010Associated cell lines:
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Pellestor F., Monzo C., Nadal L., De Vos J., Hamamah S.
P56 Acquisition of a trisomy 20 in the human embryonic stem cell line HD90
Pellestor F. et al. P56 Acquisition of a trisomy 20 in the human embryonic stem cell line HD90. . 2010-05-00. DOI: 10.1016/s1472-6483(10)62372-3 UHOMe001-A 2010-05-00 2010-05-00 DOI: 10.1016/s1472-6483(10)62372-3Associated cell lines:
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Singh H, Mok P, Balakrishnan T, Rahmat SN, Zweigerdt R
Up-scaling single cell-inoculated suspension culture of human embryonic stem cells
Singh H et al. Up-scaling single cell-inoculated suspension culture of human embryonic stem cells. . 2010-05-00. Pubmed ID: 20363202; DOI: 10.1016/j.scr.2010.03.001 ESi049-A 2010-05-00 2010-05-00 PubMed: 20363202 DOI: 10.1016/j.scr.2010.03.001Associated cell lines:
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Hovatta O, Jaconi M, Töhönen V, Béna F, Gimelli S, Bosman A, Holm F, Wyder S, Zdobnov EM, Irion O, Andrews PW, Antonarakis SE, Zucchelli M, Kere J, Feki A
A teratocarcinoma-like human embryonic stem cell (hESC) line and four hESC lines reveal potentially oncogenic genomic changes
Hovatta O et al. A teratocarcinoma-like human embryonic stem cell (hESC) line and four hESC lines reveal potentially oncogenic genomic changes. . 2010-04-23. Pubmed ID: 20428235; DOI: 10.1371/journal.pone.0010263; PMC: PMC2859053 KIe005-AKIe019-AWAe001-AUNIGEe001-A 2010-04-23 2010-04-23 PubMed: 20428235 DOI: 10.1371/journal.pone.0010263Associated cell lines:
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Rajala K, Lindroos B, Hussein SM, Lappalainen RS, Pekkanen-Mattila M, Inzunza J, Rozell B, Miettinen S, Narkilahti S, Kerkelä E, Aalto-Setälä K, Otonkoski T, Suuronen R, Hovatta O, Skottman H
A defined and xeno-free culture method enabling the establishment of clinical-grade human embryonic, induced pluripotent and adipose stem cells
Rajala K et al. A defined and xeno-free culture method enabling the establishment of clinical-grade human embryonic, induced pluripotent and adipose stem cells. . 2010-04-19. Pubmed ID: 20419109; DOI: 10.1371/journal.pone.0010246; PMC: PMC2856688 UTAe001-AUTAe002-AUTAe004-AUTAe005-A 2010-04-19 2010-04-19 PubMed: 20419109 DOI: 10.1371/journal.pone.0010246 -
Aguilar-Gallardo C, Poo M, Gomez E, Galan A, Sanchez E, Marques-Mari A, Ruiz V, Medrano J, Riboldi M, Valbuena D, Simon C
Derivation, characterization, differentiation, and registration of seven human embryonic stem cell lines (VAL-3, -4, -5, -6M, -7, -8, and -9) on human feeder
Aguilar-Gallardo C et al. Derivation, characterization, differentiation, and registration of seven human embryonic stem cell lines (VAL-3, -4, -5, -6M, -7, -8, and -9) on human feeder. . 2010-04-00. Pubmed ID: 20186513; DOI: 10.1007/s11626-010-9285-3 ESe011-AESe012-AESe013-AESe017-AESe018-AESe019-AESe021-A 2010-04-00 2010-04-00 PubMed: 20186513 DOI: 10.1007/s11626-010-9285-3 -
Skottman H
Derivation and characterization of three new human embryonic stem cell lines in Finland
Skottman H. Derivation and characterization of three new human embryonic stem cell lines in Finland. . 2010-04-00. Pubmed ID: 20177999; DOI: 10.1007/s11626-010-9286-2 UTAe006-AUTAe007-AUTAe008-A 2010-04-00 2010-04-00 PubMed: 20177999 DOI: 10.1007/s11626-010-9286-2 -
Aflatoonian B, Ruban L, Shamsuddin S, Baker D, Andrews P, Moore H
Generation of Sheffield (Shef) human embryonic stem cell lines using a microdrop culture system
Aflatoonian B et al. Generation of Sheffield (Shef) human embryonic stem cell lines using a microdrop culture system. . 2010-04-00. Pubmed ID: 20224972; DOI: 10.1007/s11626-010-9294-2 AXORe001-AAXORe002-AUOSe003-AAXORe004-AAXORe005-AUOSe006-AAXORe007-A 2010-04-00 2010-04-00 PubMed: 20224972 DOI: 10.1007/s11626-010-9294-2Associated cell lines:
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Tropel P, Tournois J, Côme J, Varela C, Moutou C, Fragner P, Cailleret M, Laâbi Y, Peschanski M, Viville S
High-efficiency derivation of human embryonic stem cell lines following pre-implantation genetic diagnosis
Tropel P et al. High-efficiency derivation of human embryonic stem cell lines following pre-implantation genetic diagnosis. . 2010-04-00. Pubmed ID: 20217271; DOI: 10.1007/s11626-010-9300-8 INSRMe002-AINSRMe003-AINSRMe004-AINSRMe005-AINSRMe006-AINSRMe007-AINSRMe008-AINSRMe009-AINSRMe010-AINSRMe011-AINSRMe012-A 2010-04-00 2010-04-00 PubMed: 20217271 DOI: 10.1007/s11626-010-9300-8Associated cell lines:
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Bradley CK, Chami O, Peura TT, Bosman A, Dumevska B, Schmidt U, Stojanov T
Derivation of three new human embryonic stem cell lines
Bradley CK et al. Derivation of three new human embryonic stem cell lines. . 2010-04-00. Pubmed ID: 20198447; DOI: 10.1007/s11626-010-9298-y GENEAe001-A 2010-04-00 2010-04-00 PubMed: 20198447 DOI: 10.1007/s11626-010-9298-yAssociated cell lines:
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Taei A, Gourabi H, Seifinejad A, Totonchi M, Shahbazi E, Valojerdi MR, Eftekhari P, Karimian L, Baharvand H
Derivation of new human embryonic stem cell lines from preimplantation genetic screening and diagnosis-analyzed embryos
Taei A et al. Derivation of new human embryonic stem cell lines from preimplantation genetic screening and diagnosis-analyzed embryos. . 2010-04-00. Pubmed ID: 20177993; DOI: 10.1007/s11626-010-9293-3 RIe007-ARIe008-ARIe009-ARIe010-A 2010-04-00 2010-04-00 PubMed: 20177993 DOI: 10.1007/s11626-010-9293-3 -
Stephenson EL, Braude PR
Derivation of the King's College London human embryonic stem cell lines
Stephenson EL et al. Derivation of the King's College London human embryonic stem cell lines. . 2010-04-00. Pubmed ID: 20178004; DOI: 10.1007/s11626-010-9276-4 KCLe004-AKCLe005-AKCLe006-AKCLe007-AKCLe008-A 2010-04-00 2010-04-00 PubMed: 20178004 DOI: 10.1007/s11626-010-9276-4 -
Camarasa MV, Kerr RW, Sneddon SF, Bates N, Shaw L, Oldershaw RA, Small F, Baxter MA, Mckay TR, Brison DR, Kimber SJ
Derivation of Man-1 and Man-2 research grade human embryonic stem cell lines
Camarasa MV et al. Derivation of Man-1 and Man-2 research grade human embryonic stem cell lines. . 2010-04-00. Pubmed ID: 20177994; DOI: 10.1007/s11626-010-9291-5 UMANe001-ACMFTe001-A 2010-04-00 2010-04-00 PubMed: 20177994 DOI: 10.1007/s11626-010-9291-5Associated cell lines:
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Lagarkova MA, Eremeev AV, Svetlakov AV, Rubtsov NB, Kiselev SL
Human embryonic stem cell lines isolation, cultivation, and characterization
Lagarkova MA et al. Human embryonic stem cell lines isolation, cultivation, and characterization. . 2010-04-00. Pubmed ID: 20178000; DOI: 10.1007/s11626-010-9282-6 RASe001-ARASe002-ARASe003-A 2010-04-00 2010-04-00 PubMed: 20178000 DOI: 10.1007/s11626-010-9282-6 -
Candan ZN, Kahraman S
Establishment and characterization of human embryonic stem cell lines, Turkey perspectives
Candan ZN et al. Establishment and characterization of human embryonic stem cell lines, Turkey perspectives. . 2010-04-00. Pubmed ID: 20349214; DOI: 10.1007/s11626-010-9299-x IMHe001-AIMHe002-AIMHe003-AIMHe004-AIMHe005-AIMHe006-AIMHe007-AIMHe008-AIMHe009-AIMHe010-AIMHe011-AIMHe012-AIMHe013-AIMHe014-AIMHe015-AIMHe016-AIMHe017-AIMHe018-A 2010-04-00 2010-04-00 PubMed: 20349214 DOI: 10.1007/s11626-010-9299-x -
Giorgetti A, Montserrat N, Rodriguez-Piza I, Azqueta C, Veiga A, Izpisúa Belmonte JC
Generation of induced pluripotent stem cells from human cord blood cells with only two factors: Oct4 and Sox2
Giorgetti A et al. Generation of induced pluripotent stem cells from human cord blood cells with only two factors: Oct4 and Sox2. . 2010-04-00. Pubmed ID: 20360773; DOI: 10.1038/nprot.2010.16 ESi033-AESi034-AESi034-BESi038-AESi038-BESi038-C 2010-04-00 2010-04-00 PubMed: 20360773 DOI: 10.1038/nprot.2010.16 -
Ström S, Holm F, Bergström R, Strömberg AM, Hovatta O
Derivation of 30 human embryonic stem cell lines--improving the quality
Ström S et al. Derivation of 30 human embryonic stem cell lines--improving the quality. . 2010-04-00. Pubmed ID: 20198446; DOI: 10.1007/s11626-010-9308-0; PMC: PMC2855803 KIe001-AKIe002-AKIe003-AKIe004-AKIe005-AKIe006-AKIe007-AKIe008-AKIe009-AKIe010-AKIe011-AKIe012-AKIe013-AKIe014-AKIe015-AKIe016-AKIe017-AKIe018-AKIe019-AKIe020-AKIe021-AKIe022-AKIe023-AKIe024-AKIe025-AKIe026-AKIe027-AKIe028-AKIe029-AKIe031-A 2010-04-00 2010-04-00 PubMed: 20198446 DOI: 10.1007/s11626-010-9308-0 -
Harkness L, Rasmussen IA, Erb K, Kassem M
Derivation and characterisation of hESC lines from supernumerary embryos, experience from Odense, Denmark
Harkness L et al. Derivation and characterisation of hESC lines from supernumerary embryos, experience from Odense, Denmark. . 2010-04-00. Pubmed ID: 20198448; DOI: 10.1007/s11626-010-9281-7 SDUe002-ASDUe003-ASDUe004-ASDUe005-ASDUe007-A 2010-04-00 2010-04-00 PubMed: 20198448 DOI: 10.1007/s11626-010-9281-7 -
Sivarajah S, Raj GS, Mathews AJ, Sahib NB, Hwang WS, Crook JM
The generation of GLP-grade human embryonic stem cell banks from four clinical-grade cell lines for preclinical research
Sivarajah S et al. The generation of GLP-grade human embryonic stem cell banks from four clinical-grade cell lines for preclinical research. . 2010-04-00. Pubmed ID: 20177998; DOI: 10.1007/s11626-010-9287-1 SSCCe003-ASSCCe004-ASSCCe007-ASSCCe008-A 2010-04-00 2010-04-00 PubMed: 20177998 DOI: 10.1007/s11626-010-9287-1Associated cell lines:
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Englund MC, Caisander G, Noaksson K, Emanuelsson K, Lundin K, Bergh C, Hansson C, Semb H, Strehl R, Hyllner J
The establishment of 20 different human embryonic stem cell lines and subclones; a report on derivation, culture, characterisation and banking
Englund MC et al. The establishment of 20 different human embryonic stem cell lines and subclones; a report on derivation, culture, characterisation and banking. . 2010-04-00. Pubmed ID: 20177996; DOI: 10.1007/s11626-010-9289-z CEBe034-A-1CEBe002-ACEBe006-ACEBe007-ACEBe011-ACEBe012-ACEBe013-ACEBe014-ACEBe015-ACEBe017-ACEBe018-ACEBe022-ACEBe023-ACEBe027-ACEBe031-ACEBe032-ACEBe033-ACEBe034-ACEBe002-A-1CEBe002-A-3 2010-04-00 2010-04-00 PubMed: 20177996 DOI: 10.1007/s11626-010-9289-z -
Priddle H, Allegrucci C, Burridge P, Munoz M, Smith NM, Devlin L, Sjoblom C, Chamberlain S, Watson S, Young LE, Denning C
Derivation and characterisation of the human embryonic stem cell lines, NOTT1 and NOTT2
Priddle H et al. Derivation and characterisation of the human embryonic stem cell lines, NOTT1 and NOTT2. . 2010-04-00. Pubmed ID: 20177995; DOI: 10.1007/s11626-010-9290-6 UNOTe001-AUNOTe002-A 2010-04-00 2010-04-00 PubMed: 20177995 DOI: 10.1007/s11626-010-9290-6Associated cell lines:
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Aran B, Rodríguez-Pizà I, Raya A, Consiglio A, Muñoz Y, Barri PN, Izpisúa JC, Veiga A
Derivation of human embryonic stem cells at the Center of Regenerative Medicine in Barcelona
Aran B et al. Derivation of human embryonic stem cells at the Center of Regenerative Medicine in Barcelona. . 2010-04-00. Pubmed ID: 20177997; DOI: 10.1007/s11626-010-9288-0 ESe009-AESe010-AESe014-AESe015-AESe016-AESe022-AESe023-AESe024-AESe025-A 2010-04-00 2010-04-00 PubMed: 20177997 DOI: 10.1007/s11626-010-9288-0 -
Mateizel I, Spits C, De Rycke M, Liebaers I, Sermon K
Derivation, culture, and characterization of VUB hESC lines
Mateizel I et al. Derivation, culture, and characterization of VUB hESC lines. . 2010-04-00. Pubmed ID: 20224973; DOI: 10.1007/s11626-010-9284-4 VUBe006-AVUBe007-AVUBe008-AVUBe009-AVUBe010-AVUBe011-AVUBe012-AVUBe013-AVUBe014-AVUBe015-AVUBe016-AVUBe017-AVUBe018-AVUBe019-AVUBe020-AVUBe021-AVUBe022-AVUBe023-AVUBe024-AVUBe028-A 2010-04-00 2010-04-00 PubMed: 20224973 DOI: 10.1007/s11626-010-9284-4 -
Venu P, Chakraborty S, Inamdar MS
Analysis of long-term culture properties and pluripotent character of two sibling human embryonic stem cell lines derived from discarded embryos
Venu P et al. Analysis of long-term culture properties and pluripotent character of two sibling human embryonic stem cell lines derived from discarded embryos. . 2010-04-00. Pubmed ID: 20178003; DOI: 10.1007/s11626-010-9277-3; PMC: PMC2855808 JNCSRe001-AJNCSRe002-AJNCSRe002-A-1JNCSRe002-A-2 2010-04-00 2010-04-00 PubMed: 20178003 DOI: 10.1007/s11626-010-9277-3Associated cell lines:
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Sidhu KS, Ryan JP, Lees JG, Tuch BE
Derivation of a new human embryonic stem cell line, Endeavour-2, and its characterization
Sidhu KS et al. Derivation of a new human embryonic stem cell line, Endeavour-2, and its characterization. . 2010-04-00. Pubmed ID: 20178001; DOI: 10.1007/s11626-010-9280-8 POWHe002-A 2010-04-00 2010-04-00 PubMed: 20178001 DOI: 10.1007/s11626-010-9280-8Associated cell lines:
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Zachar V, Prasad SM, Weli SC, Gabrielsen A, Petersen K, Petersen MB, Fink T
The effect of human embryonic stem cells (hESCs) long-term normoxic and hypoxic cultures on the maintenance of pluripotency
Zachar V et al. The effect of human embryonic stem cells (hESCs) long-term normoxic and hypoxic cultures on the maintenance of pluripotency. . 2010-04-00. Pubmed ID: 20177991; DOI: 10.1007/s11626-010-9305-3 AAUe001-AAAUe002-AAAUe003-AAAUe004-A 2010-04-00 2010-04-00 PubMed: 20177991 DOI: 10.1007/s11626-010-9305-3 -
Lagarkova MA, Shutova MV, Bogomazova AN, Vassina EM, Glazov EA, Zhang P, Rizvanov AA, Chestkov IV, Kiselev SL
Induction of pluripotency in human endothelial cells resets epigenetic profile on genome scale
Lagarkova MA et al. Induction of pluripotency in human endothelial cells resets epigenetic profile on genome scale. . 2010-03-01. Pubmed ID: 20160486; DOI: 10.4161/cc.9.5.10869 RASe001-ARASe003-A 2010-03-01 2010-03-01 PubMed: 20160486 DOI: 10.4161/cc.9.5.10869 -
Mosher JT, Pemberton TJ, Harter K, Wang C, Buzbas EO, Dvorak P, Simón C, Morrison SJ, Rosenberg NA
Lack of population diversity in commonly used human embryonic stem-cell lines
Mosher JT et al. Lack of population diversity in commonly used human embryonic stem-cell lines. . 2010-01-14. Pubmed ID: 20018958; DOI: 10.1056/nejmc0910371 MUNIe001-AMUNIe002-AMUNIe006-AWAe007-AWAe013-AWAe014-A 2010-01-14 2010-01-14 PubMed: 20018958 DOI: 10.1056/nejmc0910371Associated cell lines:
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Tsai ZY, Singh S, Yu SL, Kao LP, Chen BZ, Ho BC, Yang PC, Li SS
Identification of microRNAs regulated by activin A in human embryonic stem cells
Tsai ZY et al. Identification of microRNAs regulated by activin A in human embryonic stem cells. . 2010-01-01. Pubmed ID: 19885849; DOI: 10.1002/jcb.22385 KMUe003-A 2010-01-01 2010-01-01 PubMed: 19885849 DOI: 10.1002/jcb.22385Associated cell lines:
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Rodríguez-Pizà I, Richaud-Patin Y, Vassena R, González F, Barrero MJ, Veiga A, Raya A, Izpisúa Belmonte JC
Reprogramming of human fibroblasts to induced pluripotent stem cells under xeno-free conditions
Rodríguez-Pizà I et al. Reprogramming of human fibroblasts to induced pluripotent stem cells under xeno-free conditions. . 2010-01-00. Pubmed ID: 19890879; DOI: 10.1002/stem.248 ESi031-AESi032-A 2010-01-00 2010-01-00 PubMed: 19890879 DOI: 10.1002/stem.248 -
Takahashi K, Narita M, Yokura M, Ichisaka T, Yamanaka S
Human induced pluripotent stem cells on autologous feeders
Takahashi K et al. Human induced pluripotent stem cells on autologous feeders. . 2009-12-02. Pubmed ID: 19956543; DOI: 10.1371/journal.pone.0008067; PMC: PMC2780725 KUIFMSi004-C 2009-12-02 2009-12-02 PubMed: 19956543 DOI: 10.1371/journal.pone.0008067Associated cell lines:
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Lee JE, Kang MS, Park MH, Shim SH, Yoon TK, Chung HM, Lee DR
Evaluation of 28 human embryonic stem cell lines for use as unrelated donors in stem cell therapy: implications of HLA and ABO genotypes
Lee JE et al. Evaluation of 28 human embryonic stem cell lines for use as unrelated donors in stem cell therapy: implications of HLA and ABO genotypes. . 2010-00-00. Pubmed ID: 20587141; DOI: 10.3727/096368910x513991 CHAe001-ACHAe002-A 2010-00-00 2010-00-00 PubMed: 20587141 DOI: 10.3727/096368910x513991 -
Totonchi M, Taei A, Seifinejad A, Tabebordbar M, Rassouli H, Farrokhi A, Gourabi H, Aghdami N, Hosseini-Salekdeh G, Baharvand H
Feeder- and serum-free establishment and expansion of human induced pluripotent stem cells
Totonchi M et al. Feeder- and serum-free establishment and expansion of human induced pluripotent stem cells. . 2010-00-00. Pubmed ID: 19876814; DOI: 10.1387/ijdb.092903mt RIi001-ARIi007-ARIi008-A 2010-00-00 2010-00-00 PubMed: 19876814 DOI: 10.1387/ijdb.092903mt -
International Stem Cell Banking Initiative
Consensus guidance for banking and supply of human embryonic stem cell lines for research purposes
International Stem Cell Banking Initiative. Consensus guidance for banking and supply of human embryonic stem cell lines for research purposes. . 2009-12-00. Pubmed ID: 20016957; DOI: 10.1007/s12015-009-9085-x MUNIe001-AMUNIe002-AMUNIe003-AMUNIe004-AMUNIe005-AMUNIe006-AMUNIe007-A 2009-12-00 2009-12-00 PubMed: 20016957 DOI: 10.1007/s12015-009-9085-xAssociated cell lines:
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Sterthaus O, Zhang H, De Geyter C
[Embryonic stem cells - a scientific by-product of the assisted reproduction technology?]
Sterthaus O et al. [Embryonic stem cells - a scientific by-product of the assisted reproduction technology?]. . 2009-12-00. Pubmed ID: 19950064; DOI: 10.1024/0040-5930.66.12.839 UBASe001-A 2009-12-00 2009-12-00 PubMed: 19950064 DOI: 10.1024/0040-5930.66.12.839Associated cell lines:
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Lin G, Xie Y, Ouyang Q, Qian X, Xie P, Zhou X, Xiong B, Tan Y, Li W, Deng L, Zhou J, Zhou D, Du L, Cheng D, Liao Y, Gu Y, Zhang S, Liu T, Sun Y, Lu G
HLA-matching potential of an established human embryonic stem cell bank in China
Lin G et al. HLA-matching potential of an established human embryonic stem cell bank in China. . 2009-11-06. Pubmed ID: 19896436; DOI: 10.1016/j.stem.2009.10.009 CSUe004-ACSUe005-ANERCe002-ANERCe003-A 2009-11-06 2009-11-06 PubMed: 19896436 DOI: 10.1016/j.stem.2009.10.009Associated cell lines:
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Geens M, Mateizel I, Sermon K, De Rycke M, Spits C, Cauffman G, Devroey P, Tournaye H, Liebaers I, Van de Velde H
Human embryonic stem cell lines derived from single blastomeres of two 4-cell stage embryos
Geens M et al. Human embryonic stem cell lines derived from single blastomeres of two 4-cell stage embryos. . 2009-11-00. Pubmed ID: 19633307; DOI: 10.1093/humrep/dep262; PMC: PMC2763129 VUBe019-AVUBe020-AVUBe026-AVUBe027-A 2009-11-00 2009-11-00 PubMed: 19633307 DOI: 10.1093/humrep/dep262 -
Lee JH, Park IH, Gao Y, Li JB, Li Z, Daley GQ, Zhang K, Church GM
A robust approach to identifying tissue-specific gene expression regulatory variants using personalized human induced pluripotent stem cells
Lee JH et al. A robust approach to identifying tissue-specific gene expression regulatory variants using personalized human induced pluripotent stem cells. . 2009-11-00. Pubmed ID: 19911041; DOI: 10.1371/journal.pgen.1000718; PMC: PMC2766639 HVRDi004-B 2009-11-00 2009-11-00 PubMed: 19911041 DOI: 10.1371/journal.pgen.1000718Associated cell lines:
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Haase A, Olmer R, Schwanke K, Wunderlich S, Merkert S, Hess C, Zweigerdt R, Gruh I, Meyer J, Wagner S, Maier LS, Han DW, Glage S, Miller K, Fischer P, Schöler HR, Martin U
Generation of induced pluripotent stem cells from human cord blood
Haase A et al. Generation of induced pluripotent stem cells from human cord blood. . 2009-10-02. Pubmed ID: 19796623; DOI: 10.1016/j.stem.2009.08.021 MHHi009-A 2009-10-02 2009-10-02 PubMed: 19796623 DOI: 10.1016/j.stem.2009.08.021Associated cell lines:
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Giorgetti A, Montserrat N, Aasen T, Gonzalez F, Rodríguez-Pizà I, Vassena R, Raya A, Boué S, Barrero MJ, Corbella BA, Torrabadella M, Veiga A, Izpisua Belmonte JC
Generation of induced pluripotent stem cells from human cord blood using OCT4 and SOX2
Giorgetti A et al. Generation of induced pluripotent stem cells from human cord blood using OCT4 and SOX2. . 2009-10-02. Pubmed ID: 19796614; DOI: 10.1016/j.stem.2009.09.008; PMC: PMC2779776 ESi033-AESi034-AESi034-BESi038-BESi038-C 2009-10-02 2009-10-02 PubMed: 19796614 DOI: 10.1016/j.stem.2009.09.008 -
Sacchetti P, Sousa KM, Hall AC, Liste I, Steffensen KR, Theofilopoulos S, Parish CL, Hazenberg C, Richter LA, Hovatta O, Gustafsson JA, Arenas E
Liver X receptors and oxysterols promote ventral midbrain neurogenesis in vivo and in human embryonic stem cells
Sacchetti P et al. Liver X receptors and oxysterols promote ventral midbrain neurogenesis in vivo and in human embryonic stem cells. . 2009-10-02. Pubmed ID: 19796621; DOI: 10.1016/j.stem.2009.08.019 KIe001-A 2009-10-02 2009-10-02 PubMed: 19796621 DOI: 10.1016/j.stem.2009.08.019Associated cell lines:
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Unger C, Gao S, Cohen M, Jaconi M, Bergstrom R, Holm F, Galan A, Sanchez E, Irion O, Dubuisson JB, Giry-Laterriere M, Salmon P, Simon C, Hovatta O, Feki A
Immortalized human skin fibroblast feeder cells support growth and maintenance of both human embryonic and induced pluripotent stem cells
Unger C et al. Immortalized human skin fibroblast feeder cells support growth and maintenance of both human embryonic and induced pluripotent stem cells. . 2009-10-00. Pubmed ID: 19556288; DOI: 10.1093/humrep/dep232 KIe001-AWAe001-AWAe009-A 2009-10-00 2009-10-00 PubMed: 19556288 DOI: 10.1093/humrep/dep232 -
Lacoste A, Berenshteyn F, Brivanlou AH
An efficient and reversible transposable system for gene delivery and lineage-specific differentiation in human embryonic stem cells
Lacoste A et al. An efficient and reversible transposable system for gene delivery and lineage-specific differentiation in human embryonic stem cells. . 2009-09-04. Pubmed ID: 19733544; DOI: 10.1016/j.stem.2009.07.011 RUESe002-A 2009-09-04 2009-09-04 PubMed: 19733544 DOI: 10.1016/j.stem.2009.07.011Associated cell lines:
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Lu B, Malcuit C, Wang S, Girman S, Francis P, Lemieux L, Lanza R, Lund R
Long-term safety and function of RPE from human embryonic stem cells in preclinical models of macular degeneration
Lu B et al. Long-term safety and function of RPE from human embryonic stem cells in preclinical models of macular degeneration. . 2009-09-00. Pubmed ID: 19521979; DOI: 10.1002/stem.149 ACTe002-A 2009-09-00 2009-09-00 PubMed: 19521979 DOI: 10.1002/stem.149Associated cell lines:
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Papapetrou EP, Tomishima MJ, Chambers SM, Mica Y, Reed E, Menon J, Tabar V, Mo Q, Studer L, Sadelain M
Stoichiometric and temporal requirements of Oct4, Sox2, Klf4, and c-Myc expression for efficient human iPSC induction and differentiation
Papapetrou EP et al. Stoichiometric and temporal requirements of Oct4, Sox2, Klf4, and c-Myc expression for efficient human iPSC induction and differentiation. . 2009-08-04. Pubmed ID: 19549847; DOI: 10.1073/pnas.0904825106; PMC: PMC2722286 MSKi002-A 2009-08-04 2009-08-04 PubMed: 19549847 DOI: 10.1073/pnas.0904825106Associated cell lines:
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Cortes JL, Sanchez L, Ligero G, Gutierrez-Aranda I, Catalina P, Elosua C, Leone PE, Montes R, Bueno C, Ramos-Mejía V, Maleno I, García-Pérez JL, Menendez P
Mesenchymal stem cells facilitate the derivation of human embryonic stem cells from cryopreserved poor-quality embryos
Cortes JL et al. Mesenchymal stem cells facilitate the derivation of human embryonic stem cells from cryopreserved poor-quality embryos. . 2009-08-00. Pubmed ID: 19401322; DOI: 10.1093/humrep/dep107 ESe029-A 2009-08-00 2009-08-00 PubMed: 19401322 DOI: 10.1093/humrep/dep107Associated cell lines:
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Eiselleova L, Matulka K, Kriz V, Kunova M, Schmidtova Z, Neradil J, Tichy B, Dvorakova D, Pospisilova S, Hampl A, Dvorak P
A complex role for FGF-2 in self-renewal, survival, and adhesion of human embryonic stem cells
Eiselleova L et al. A complex role for FGF-2 in self-renewal, survival, and adhesion of human embryonic stem cells. . 2009-08-00. Pubmed ID: 19544431; DOI: 10.1002/stem.128; PMC: PMC2798073 MUNIe005-AMUNIe007-A 2009-08-00 2009-08-00 PubMed: 19544431 DOI: 10.1002/stem.128Associated cell lines:
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Raya A, Rodríguez-Pizà I, Guenechea G, Vassena R, Navarro S, Barrero MJ, Consiglio A, Castellà M, Río P, Sleep E, González F, Tiscornia G, Garreta E, Aasen T, Veiga A, Verma IM, Surrallés J, Bueren J, Izpisúa Belmonte JC
Disease-corrected haematopoietic progenitors from Fanconi anaemia induced pluripotent stem cells
Raya A et al. Disease-corrected haematopoietic progenitors from Fanconi anaemia induced pluripotent stem cells. . 2009-07-02. Pubmed ID: 19483674; DOI: 10.1038/nature08129; PMC: PMC2720823 ESi005-AESi005-B 2009-07-02 2009-07-02 PubMed: 19483674 DOI: 10.1038/nature08129 -
Martín-Ibáñez R, Strömberg AM, Hovatta O, Canals JM
Cryopreservation of dissociated human embryonic stem cells in the presence of ROCK inhibitor
Martín-Ibáñez R et al. Cryopreservation of dissociated human embryonic stem cells in the presence of ROCK inhibitor. . 2009-07-00. Pubmed ID: 19585460; DOI: 10.1002/9780470151808.sc01c08s10 KIe002-AKIe019-A 2009-07-00 2009-07-00 PubMed: 19585460 DOI: 10.1002/9780470151808.sc01c08s10 -
Catalina P, Bueno C, Montes R, Nieto A, Ligero G, Sanchez L, Jara M, Rasillo A, Orfao A, Cigudosa J, Hovatta O, Greaves M, Menendez P
Genetic stability of human embryonic stem cells: A first-step toward the development of potential hESC-based systems for modeling childhood leukemia
Catalina P et al. Genetic stability of human embryonic stem cells: A first-step toward the development of potential hESC-based systems for modeling childhood leukemia. . 2009-07-00. Pubmed ID: 18930318; DOI: 10.1016/j.leukres.2008.08.028 KIe001-AKIe005-A 2009-07-00 2009-07-00 PubMed: 18930318 DOI: 10.1016/j.leukres.2008.08.028 -
Yu J, Hu K, Smuga-Otto K, Tian S, Stewart R, Slukvin II, Thomson JA
Human induced pluripotent stem cells free of vector and transgene sequences
Yu J et al. Human induced pluripotent stem cells free of vector and transgene sequences. . 2009-05-08. Pubmed ID: 19325077; DOI: 10.1126/science.1172482; PMC: PMC2758053 WAi001-AWAi001-BWAi001-C 2009-05-08 2009-05-08 PubMed: 19325077 DOI: 10.1126/science.1172482 -
Friling S, Andersson E, Thompson LH, Jönsson ME, Hebsgaard JB, Nanou E, Alekseenko Z, Marklund U, Kjellander S, Volakakis N, Hovatta O, El Manira A, Björklund A, Perlmann T, Ericson J
Efficient production of mesencephalic dopamine neurons by Lmx1a expression in embryonic stem cells
Friling S et al. Efficient production of mesencephalic dopamine neurons by Lmx1a expression in embryonic stem cells. . 2009-05-05. Pubmed ID: 19383789; DOI: 10.1073/pnas.0902396106; PMC: PMC2671325 KIe005-AKIe008-AKIe019-A 2009-05-05 2009-05-05 PubMed: 19383789 DOI: 10.1073/pnas.0902396106 -
Deleu S, Gonzalez-Merino E, Gaspard N, Nguyen TM, Vanderhaeghen P, Lagneaux L, Toungouz M, Englert Y, Devreker F
Human cystic fibrosis embryonic stem cell lines derived on placental mesenchymal stromal cells
Deleu S et al. Human cystic fibrosis embryonic stem cell lines derived on placental mesenchymal stromal cells. . 2009-05-00. Pubmed ID: 19549452; DOI: 10.1016/s1472-6483(10)60018-1 ULBe001-AULBe002-AULBe003-AULBe004-AULBe005-A 2009-05-00 2009-05-00 PubMed: 19549452 DOI: 10.1016/s1472-6483(10)60018-1 -
De Sousa PA, Gardner J, Sneddon S, Pells S, Tye BJ, Dand P, Collins DM, Stewart K, Shaw L, Przyborski S, Cooke M, McLaughlin KJ, Kimber SJ, Lieberman BA, Wilmut I, Brison DR
Clinically failed eggs as a source of normal human embryo stem cells
De Sousa PA et al. Clinically failed eggs as a source of normal human embryo stem cells. . 2009-05-00. Pubmed ID: 19393594; DOI: 10.1016/j.scr.2009.01.002 RCe005-A 2009-05-00 2009-05-00 PubMed: 19393594 DOI: 10.1016/j.scr.2009.01.002Associated cell lines:
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Liu W, Yin Y, Long X, Luo Y, Jiang Y, Zhang W, Du H, Li S, Zheng Y, Li Q, Chen X, Liao B, Xiao G, Wang W, Sun X
Derivation and characterization of human embryonic stem cell lines from poor quality embryos
Liu W et al. Derivation and characterization of human embryonic stem cell lines from poor quality embryos. . 2009-04-00. Pubmed ID: 19376483; DOI: 10.1016/s1673-8527(08)60110-1 GZHMCe001-AGZHMCe002-AGZHMCe003-AGZHMCe004-A 2009-04-00 2009-04-00 PubMed: 19376483 DOI: 10.1016/s1673-8527(08)60110-1Associated cell lines:
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Kumar N, Hinduja I, Nagvenkar P, Pillai L, Zaveri K, Mukadam L, Telang J, Desai S, Mangoli V, Mangoli R, Padgaonkar S, Kaur G, Puri C, Bhartiya D
Derivation and characterization of two genetically unique human embryonic stem cell lines on in-house-derived human feeders
Kumar N et al. Derivation and characterization of two genetically unique human embryonic stem cell lines on in-house-derived human feeders. . 2009-04-00. Pubmed ID: 18699724; DOI: 10.1089/scd.2008.0234 NIRRHe001-ANIRRHe002-A 2009-04-00 2009-04-00 PubMed: 18699724 DOI: 10.1089/scd.2008.0234Associated cell lines:
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Inamdar MS, Venu P, Srinivas MS, Rao K, VijayRaghavan K
Derivation and characterization of two sibling human embryonic stem cell lines from discarded grade III embryos
Inamdar MS et al. Derivation and characterization of two sibling human embryonic stem cell lines from discarded grade III embryos. . 2009-04-00. Pubmed ID: 18616385; DOI: 10.1089/scd.2008.0131 JNCSRe001-AJNCSRe002-AJNCSRe002-A-1JNCSRe002-A-2JNCSRe002-A-3 2009-04-00 2009-04-00 PubMed: 18616385 DOI: 10.1089/scd.2008.0131Associated cell lines:
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Wang J, Lin G, Zhao HP, Lu GX
[Spontaneous differentiation of human embryonic stem cells into hematopoietic cells]
Wang J et al. [Spontaneous differentiation of human embryonic stem cells into hematopoietic cells]. . 2009-04-00. Pubmed ID: 19403374 CSUe001-A 2009-04-00 2009-04-00 PubMed: 19403374Associated cell lines:
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Sundberg M, Jansson L, Ketolainen J, Pihlajamäki H, Suuronen R, Skottman H, Inzunza J, Hovatta O, Narkilahti S
CD marker expression profiles of human embryonic stem cells and their neural derivatives, determined using flow-cytometric analysis, reveal a novel CD marker for exclusion of pluripotent stem cells
Sundberg M et al. CD marker expression profiles of human embryonic stem cells and their neural derivatives, determined using flow-cytometric analysis, reveal a novel CD marker for exclusion of pluripotent stem cells. . 2009-03-00. Pubmed ID: 19383417; DOI: 10.1016/j.scr.2008.08.001 KIe001-AKIe007-AKIe009-AKIe011-AKIe019-A 2009-03-00 2009-03-00 PubMed: 19383417 DOI: 10.1016/j.scr.2008.08.001 -
Chen AE, Egli D, Niakan K, Deng J, Akutsu H, Yamaki M, Cowan C, Fitz-Gerald C, Zhang K, Melton DA, Eggan K
Optimal timing of inner cell mass isolation increases the efficiency of human embryonic stem cell derivation and allows generation of sibling cell lines
Chen AE et al. Optimal timing of inner cell mass isolation increases the efficiency of human embryonic stem cell derivation and allows generation of sibling cell lines. . 2009-02-06. Pubmed ID: 19200798; DOI: 10.1016/j.stem.2008.12.001; PMC: PMC3335201 HVRDe001-AHVRDe002-AHVRDe003-AHVRDe004-AHVRDe005-AHVRDe006-AHVRDe007-AHVRDe008-AHVRDe009-AHVRDe010-AHVRDe011-AHVRDe012-AHVRDe013-AHVRDe014-AHVRDe015-AHVRDe016-AHVRDe017-A 2009-02-06 2009-02-06 PubMed: 19200798 DOI: 10.1016/j.stem.2008.12.001 -
Hicks AU, Lappalainen RS, Narkilahti S, Suuronen R, Corbett D, Sivenius J, Hovatta O, Jolkkonen J
Transplantation of human embryonic stem cell-derived neural precursor cells and enriched environment after cortical stroke in rats: cell survival and functional recovery
Hicks AU et al. Transplantation of human embryonic stem cell-derived neural precursor cells and enriched environment after cortical stroke in rats: cell survival and functional recovery. . 2009-02-00. Pubmed ID: 19175403; DOI: 10.1111/j.1460-9568.2008.06599.x KIe001-A 2009-02-00 2009-02-00 PubMed: 19175403 DOI: 10.1111/j.1460-9568.2008.06599.xAssociated cell lines:
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Assou S, Cerecedo D, Tondeur S, Pantesco V, Hovatta O, Klein B, Hamamah S, De Vos J
A gene expression signature shared by human mature oocytes and embryonic stem cells
Assou S et al. A gene expression signature shared by human mature oocytes and embryonic stem cells. . 2009-01-08. Pubmed ID: 19128516; DOI: 10.1186/1471-2164-10-10; PMC: PMC2628676 KIe001-AUHOMe001-A 2009-01-08 2009-01-08 PubMed: 19128516 DOI: 10.1186/1471-2164-10-10Associated cell lines:
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Prokhorova TA, Harkness LM, Frandsen U, Ditzel N, Schrøder HD, Burns JS, Kassem M
Teratoma formation by human embryonic stem cells is site dependent and enhanced by the presence of Matrigel
Prokhorova TA et al. Teratoma formation by human embryonic stem cells is site dependent and enhanced by the presence of Matrigel. . 2009-01-00. Pubmed ID: 18393673; DOI: 10.1089/scd.2007.0266 SDUe001-ASDUe002-ASDUe003-ASDUe004-ASDUe005-ASDUe007-A 2009-01-00 2009-01-00 PubMed: 18393673 DOI: 10.1089/scd.2007.0266 -
Verlinsky Y, Strelchenko N, Kukharenko V, Zech NH, Shkumatov A, Zlatopolsky Z, Kuliev A
Impact of meiotic and mitotic non-disjunction on generation of human embryonic stem cell lines
Verlinsky Y et al. Impact of meiotic and mitotic non-disjunction on generation of human embryonic stem cell lines. . 2009-01-00. Pubmed ID: 19146778; DOI: 10.1016/s1472-6483(10)60433-6 RGIe063-ARGIe067-ARGIe068-ARGIe088-ARGIe089-ARGIe090-ARGIe103-ARGIe110-ARGIe112-ARGIe121-ARGIe122-ARGIe130-ARGIe139-ARGIe142-ARGIe144-ARGIe152-A 2009-01-00 2009-01-00 PubMed: 19146778 DOI: 10.1016/s1472-6483(10)60433-6 -
Lu SJ, Feng Q, Park JS, Vida L, Lee BS, Strausbauch M, Wettstein PJ, Honig GR, Lanza R
Biologic properties and enucleation of red blood cells from human embryonic stem cells
Lu SJ et al. Biologic properties and enucleation of red blood cells from human embryonic stem cells. . 2008-12-01. Pubmed ID: 18713948; DOI: 10.1182/blood-2008-05-157198; PMC: PMC2597123 HVRDe003-AACTe001-AWAe001-A 2008-12-01 2008-12-01 PubMed: 18713948 DOI: 10.1182/blood-2008-05-157198Associated cell lines:
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Feki A, Hovatta O, Jaconi M
Derivation of human embryonic stem cell lines from single cells of 4-cell stage embryos: be aware of the risks
Feki A et al. Derivation of human embryonic stem cell lines from single cells of 4-cell stage embryos: be aware of the risks. . 2008-12-00. Pubmed ID: 18854403; DOI: 10.1093/humrep/den369 UNIGEe001-A 2008-12-00 2008-12-00 PubMed: 18854403 DOI: 10.1093/humrep/den369Associated cell lines:
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Kubikova I, Konecna H, Sedo O, Zdrahal Z, Rehulka P, Hribkova H, Rehulkova H, Hampl A, Chmelik J, Dvorak P
Proteomic profiling of human embryonic stem cell-derived microvesicles reveals a risk of transfer of proteins of bovine and mouse origin
Kubikova I et al. Proteomic profiling of human embryonic stem cell-derived microvesicles reveals a risk of transfer of proteins of bovine and mouse origin. . 2009-00-00. Pubmed ID: 19401887; DOI: 10.1080/14653240802595531 MUNIe005-AMUNIe007-A 2009-00-00 2009-00-00 PubMed: 19401887 DOI: 10.1080/14653240802595531Associated cell lines:
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Aasen T, Raya A, Barrero MJ, Garreta E, Consiglio A, Gonzalez F, Vassena R, Bilić J, Pekarik V, Tiscornia G, Edel M, Boué S, Izpisúa Belmonte JC
Efficient and rapid generation of induced pluripotent stem cells from human keratinocytes
Aasen T et al. Efficient and rapid generation of induced pluripotent stem cells from human keratinocytes. . 2008-11-00. Pubmed ID: 18931654; DOI: 10.1038/nbt.1503 ESi028-AESi008-A 2008-11-00 2008-11-00 PubMed: 18931654 DOI: 10.1038/nbt.1503 -
Sun X, Long X, Yin Y, Jiang Y, Chen X, Liu W, Zhang W, Du H, Li S, Zheng Y, Kong S, Pang Q, Shi Y, Huang Y, Huang S, Liao B, Xiao G, Wang W
Similar biological characteristics of human embryonic stem cell lines with normal and abnormal karyotypes
Sun X et al. Similar biological characteristics of human embryonic stem cell lines with normal and abnormal karyotypes. . 2008-10-00. Pubmed ID: 18611919; DOI: 10.1093/humrep/den137; PMC: PMC2538585 GZHMCe001-AGZHMCe003-A 2008-10-00 2008-10-00 PubMed: 18611919 DOI: 10.1093/humrep/den137Associated cell lines:
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Feki A, Bosman A, Dubuisson JB, Irion O, Dahoun S, Pelte MF, Hovatta O, Jaconi ME
Derivation of the first Swiss human embryonic stem cell line from a single blastomere of an arrested four-cell stage embryo
Feki A et al. Derivation of the first Swiss human embryonic stem cell line from a single blastomere of an arrested four-cell stage embryo. . 2008-09-20. Pubmed ID: 18803035; DOI: 10.4414/smw.2008.12385 UNIGEe001-A 2008-09-20 2008-09-20 PubMed: 18803035 DOI: 10.4414/smw.2008.12385Associated cell lines:
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Grinnemo KH, Genead R, Kumagai-Braesch M, Andersson A, Danielsson C, Månsson-Broberg A, Dellgren G, Strömberg AM, Ekberg H, Hovatta O, Sylvén C, Corbascio M
Costimulation blockade induces tolerance to HESC transplanted to the testis and induces regulatory T-cells to HESC transplanted into the heart
Grinnemo KH et al. Costimulation blockade induces tolerance to HESC transplanted to the testis and induces regulatory T-cells to HESC transplanted into the heart. . 2008-07-00. Pubmed ID: 18467659; DOI: 10.1634/stemcells.2008.0111 KIe019-A 2008-07-00 2008-07-00 PubMed: 18467659 DOI: 10.1634/stemcells.2008.0111Associated cell lines:
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De Temmerman N, Seneca S, Van Steirteghem A, Haentjens P, Van der Elst J, Liebaers I, Sermon KD
CTG repeat instability in a human embryonic stem cell line carrying the myotonic dystrophy type 1 mutation
De Temmerman N et al. CTG repeat instability in a human embryonic stem cell line carrying the myotonic dystrophy type 1 mutation. . 2008-07-00. Pubmed ID: 18577525; DOI: 10.1093/molehr/gan034 VUBe001-AVUBe003-AVUBe004-A 2008-07-00 2008-07-00 PubMed: 18577525 DOI: 10.1093/molehr/gan034 -
Peura T, Bosman A, Chami O, Jansen RP, Texlova K, Stojanov T
Karyotypically normal and abnormal human embryonic stem cell lines derived from PGD-analyzed embryos
Peura T et al. Karyotypically normal and abnormal human embryonic stem cell lines derived from PGD-analyzed embryos. . 2008-06-00. Pubmed ID: 18386991; DOI: 10.1089/clo.2007.0062 GENEAe002-AGENEAe003-AGENEAe004-AGENEAe005-AGENEAe006-AGENEAe007-AGENEAe008-AGENEAe009-AGENEAe010-AGENEAe011-AGENEAe012-A 2008-06-00 2008-06-00 PubMed: 18386991 DOI: 10.1089/clo.2007.0062Associated cell lines:
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Chavez SL, Meneses JJ, Nguyen HN, Kim SK, Pera RA
Characterization of six new human embryonic stem cell lines (HSF7, -8, -9, -10, -12, and -13) derived under minimal-animal component conditions
Chavez SL et al. Characterization of six new human embryonic stem cell lines (HSF7, -8, -9, -10, -12, and -13) derived under minimal-animal component conditions. . 2008-06-00. Pubmed ID: 18513167; DOI: 10.1089/scd.2007.0216 SUSMe001-ASUSMe002-ASUSMe003-ASUSMe004-ASUSMe005-ASUSMe006-A 2008-06-00 2008-06-00 PubMed: 18513167 DOI: 10.1089/scd.2007.0216Associated cell lines:
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Mateizel I, De Becker A, Van de Velde H, De Rycke M, Van Steirteghem A, Cornelissen R, Van der Elst J, Liebaers I, Van Riet I, Sermon K
Efficient differentiation of human embryonic stem cells into a homogeneous population of osteoprogenitor-like cells
Mateizel I et al. Efficient differentiation of human embryonic stem cells into a homogeneous population of osteoprogenitor-like cells. . 2008-05-00. Pubmed ID: 18492382; DOI: 10.1016/s1472-6483(10)60490-7 VUBe001-AVUBe003-A 2008-05-00 2008-05-00 PubMed: 18492382 DOI: 10.1016/s1472-6483(10)60490-7 -
Braam SR, Denning C, van den Brink S, Kats P, Hochstenbach R, Passier R, Mummery CL
Improved genetic manipulation of human embryonic stem cells
Braam SR et al. Improved genetic manipulation of human embryonic stem cells. . 2008-05-00. Pubmed ID: 18391958; DOI: 10.1038/nmeth.1200 LUMCe001-ALUMCe002-ALUMCe003-ALUMCe004-AUNOTe001-AUNOTe002-A 2008-05-00 2008-05-00 PubMed: 18391958 DOI: 10.1038/nmeth.1200Associated cell lines:
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Kroon E, Martinson LA, Kadoya K, Bang AG, Kelly OG, Eliazer S, Young H, Richardson M, Smart NG, Cunningham J, Agulnick AD, D'Amour KA, Carpenter MK, Baetge EE
Pancreatic endoderm derived from human embryonic stem cells generates glucose-responsive insulin-secreting cells in vivo
Kroon E et al. Pancreatic endoderm derived from human embryonic stem cells generates glucose-responsive insulin-secreting cells in vivo. . 2008-04-00. Pubmed ID: 18288110; DOI: 10.1038/nbt1393 VIACe005-AVCYTe001-A 2008-04-00 2008-04-00 PubMed: 18288110 DOI: 10.1038/nbt1393Associated cell lines:
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Kiprilov EN, Awan A, Desprat R, Velho M, Clement CA, Byskov AG, Andersen CY, Satir P, Bouhassira EE, Christensen ST, Hirsch RE
Human embryonic stem cells in culture possess primary cilia with hedgehog signaling machinery
Kiprilov EN et al. Human embryonic stem cells in culture possess primary cilia with hedgehog signaling machinery. . 2008-03-10. Pubmed ID: 18332216; DOI: 10.1083/jcb.200706028; PMC: PMC2265400 KUe003-A 2008-03-10 2008-03-10 PubMed: 18332216 DOI: 10.1083/jcb.200706028Associated cell lines:
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Ullmann U, Gilles C, De Rycke M, Van de Velde H, Sermon K, Liebaers I
GSK-3-specific inhibitor-supplemented hESC medium prevents the epithelial-mesenchymal transition process and the up-regulation of matrix metalloproteinases in hESCs cultured in feeder-free conditions
Ullmann U et al. GSK-3-specific inhibitor-supplemented hESC medium prevents the epithelial-mesenchymal transition process and the up-regulation of matrix metalloproteinases in hESCs cultured in feeder-free conditions. . 2008-03-00. Pubmed ID: 18263607; DOI: 10.1093/molehr/gan001 VUBe001-AVUBe002-AVUBe004-A 2008-03-00 2008-03-00 PubMed: 18263607 DOI: 10.1093/molehr/gan001 -
Freund C, Ward-van Oostwaard D, Monshouwer-Kloots J, van den Brink S, van Rooijen M, Xu X, Zweigerdt R, Mummery C, Passier R
Insulin redirects differentiation from cardiogenic mesoderm and endoderm to neuroectoderm in differentiating human embryonic stem cells
Freund C et al. Insulin redirects differentiation from cardiogenic mesoderm and endoderm to neuroectoderm in differentiating human embryonic stem cells. . 2008-03-00. Pubmed ID: 18096723; DOI: 10.1634/stemcells.2007-0617 LUMCe003-ALUMCe004-A 2008-03-00 2008-03-00 PubMed: 18096723 DOI: 10.1634/stemcells.2007-0617Associated cell lines:
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Sidhu KS, Ryan JP, Tuch BE
Derivation of a new human embryonic stem cell line, endeavour-1, and its clonal propagation
Sidhu KS et al. Derivation of a new human embryonic stem cell line, endeavour-1, and its clonal propagation. . 2008-02-00. Pubmed ID: 18271699; DOI: 10.1089/scd.2007.0055 POWHe001-APOWHe001-A-1POWHe001-A-2POWHe001-A-3POWHe001-A-4 2008-02-00 2008-02-00 PubMed: 18271699 DOI: 10.1089/scd.2007.0055Associated cell lines:
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Lerou PH, Yabuuchi A, Huo H, Takeuchi A, Shea J, Cimini T, Ince TA, Ginsburg E, Racowsky C, Daley GQ
Human embryonic stem cell derivation from poor-quality embryos
Lerou PH et al. Human embryonic stem cell derivation from poor-quality embryos. . 2008-02-00. Pubmed ID: 18223642; DOI: 10.1038/nbt1378 BCHe002-ABCHe003-ABCHe004-ABCHe005-ABCHe006-A 2008-02-00 2008-02-00 PubMed: 18223642 DOI: 10.1038/nbt1378 -
Turetsky T, Aizenman E, Gil Y, Weinberg N, Shufaro Y, Revel A, Laufer N, Simon A, Abeliovich D, Reubinoff BE
Laser-assisted derivation of human embryonic stem cell lines from IVF embryos after preimplantation genetic diagnosis
Turetsky T et al. Laser-assisted derivation of human embryonic stem cell lines from IVF embryos after preimplantation genetic diagnosis. . 2008-01-00. Pubmed ID: 17989069; DOI: 10.1093/humrep/dem351 HADe001-AHADe002-AHADe003-AHADe004-AHADe005-AHADe006-A 2008-01-00 2008-01-00 PubMed: 17989069 DOI: 10.1093/humrep/dem351 -
Lee MH, Hook B, Pan G, Kershner AM, Merritt C, Seydoux G, Thomson JA, Wickens M, Kimble J
Conserved regulation of MAP kinase expression by PUF RNA-binding proteins
Lee MH et al. Conserved regulation of MAP kinase expression by PUF RNA-binding proteins. . 2007-12-28. Pubmed ID: 18166083; DOI: 10.1371/journal.pgen.0030233; PMC: PMC2323325 WAe009-A-10 2007-12-28 2007-12-28 PubMed: 18166083 DOI: 10.1371/journal.pgen.0030233Associated cell lines:
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Yu J, Vodyanik MA, Smuga-Otto K, Antosiewicz-Bourget J, Frane JL, Tian S, Nie J, Jonsdottir GA, Ruotti V, Stewart R, Slukvin II, Thomson JA
Induced pluripotent stem cell lines derived from human somatic cells
Yu J et al. Induced pluripotent stem cell lines derived from human somatic cells. . 2007-12-21. Pubmed ID: 18029452; DOI: 10.1126/science.1151526 WISCi003-AWISCi004-AWISCi004-B 2007-12-21 2007-12-21 PubMed: 18029452 DOI: 10.1126/science.1151526Associated cell lines:
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Raya A, Rodríguez-Pizà I, Arán B, Consiglio A, Barri PN, Veiga A, Izpisúa Belmonte JC
Generation of cardiomyocytes from new human embryonic stem cell lines derived from poor-quality blastocysts
Raya A et al. Generation of cardiomyocytes from new human embryonic stem cell lines derived from poor-quality blastocysts. . 2008-00-00. Pubmed ID: 19028986; DOI: 10.1101/sqb.2008.73.038 ESe009-AESe010-AESe014-AESe015-AESe016-A 2008-00-00 2008-00-00 PubMed: 19028986 DOI: 10.1101/sqb.2008.73.038 -
Kim KP, Thurston A, Mummery C, Ward-van Oostwaard D, Priddle H, Allegrucci C, Denning C, Young L
Gene-specific vulnerability to imprinting variability in human embryonic stem cell lines
Kim KP et al. Gene-specific vulnerability to imprinting variability in human embryonic stem cell lines. . 2007-12-00. Pubmed ID: 17989250; DOI: 10.1101/gr.6609207; PMC: PMC2099582 UNOTe001-AUNOTe002-A 2007-12-00 2007-12-00 PubMed: 17989250 DOI: 10.1101/gr.6609207Associated cell lines:
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Takahashi K, Tanabe K, Ohnuki M, Narita M, Ichisaka T, Tomoda K, Yamanaka S
Induction of pluripotent stem cells from adult human fibroblasts by defined factors
Takahashi K et al. Induction of pluripotent stem cells from adult human fibroblasts by defined factors. . 2007-11-30. Pubmed ID: 18035408; DOI: 10.1016/j.cell.2007.11.019 KUIFMSi004-AKUIFMSi004-DKUIFMSi004-EKUIFMSi004-BKUIFMSi004-CKUIFMSi009-AKUIFMSi009-BKUIFMSi011-AKUIFMSi011-BKUIFMSi011-CKUIFMSi011-DKUIFMSi011-E 2007-11-30 2007-11-30 PubMed: 18035408 DOI: 10.1016/j.cell.2007.11.019 -
Mai Q, Yu Y, Li T, Wang L, Chen MJ, Huang SZ, Zhou C, Zhou Q
Derivation of human embryonic stem cell lines from parthenogenetic blastocysts
Mai Q et al. Derivation of human embryonic stem cell lines from parthenogenetic blastocysts. . 2007-12-00. Pubmed ID: 18071366; DOI: 10.1038/cr.2007.102 GUCASe001-AGUCASe002-A 2007-12-00 2007-12-00 PubMed: 18071366 DOI: 10.1038/cr.2007.102Associated cell lines:
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Braam SR, Denning C, Matsa E, Young LE, Passier R, Mummery CL
Feeder-free culture of human embryonic stem cells in conditioned medium for efficient genetic modification
Braam SR et al. Feeder-free culture of human embryonic stem cells in conditioned medium for efficient genetic modification. . 2008-00-00. Pubmed ID: 18772870; DOI: 10.1038/nprot.2008.140 LUMCe001-ALUMCe002-ALUMCe003-ALUMCe004-AUNOTe001-AUNOTe002-AHVRDe001-AHVRDe005-AHVRDe007-AHVRDe015-AVIACe001-AESIBIe002-ACEBe002-A-2ESIBIe003-A-4 2008-00-00 2008-00-00 PubMed: 18772870 DOI: 10.1038/nprot.2008.140 -
Ström S, Inzunza J, Grinnemo KH, Holmberg K, Matilainen E, Strömberg AM, Blennow E, Hovatta O
Mechanical isolation of the inner cell mass is effective in derivation of new human embryonic stem cell lines
Ström S et al. Mechanical isolation of the inner cell mass is effective in derivation of new human embryonic stem cell lines. . 2007-12-00. Pubmed ID: 17959612; DOI: 10.1093/humrep/dem335 KIe021-AKIe022-AKIe023-AKIe024-AKIe025-AKIe026-AKIe027-AKIe029-A 2007-12-00 2007-12-00 PubMed: 17959612 DOI: 10.1093/humrep/dem335 -
Crook JM, Peura TT, Kravets L, Bosman AG, Buzzard JJ, Horne R, Hentze H, Dunn NR, Zweigerdt R, Chua F, Upshall A, Colman A
The generation of six clinical-grade human embryonic stem cell lines
Crook JM et al. The generation of six clinical-grade human embryonic stem cell lines. . 2007-11-00. Pubmed ID: 18938745; DOI: 10.1016/j.stem.2007.10.004 SSCCe001-ASSCCe002-ASSCCe003-ASSCCe004-ASSCCe005-ASSCCe006-ASSCCe007-ASSCCe008-A 2007-11-00 2007-11-00 PubMed: 18938745 DOI: 10.1016/j.stem.2007.10.004Associated cell lines:
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Eiges R, Urbach A, Malcov M, Frumkin T, Schwartz T, Amit A, Yaron Y, Eden A, Yanuka O, Benvenisty N, Ben-Yosef D
Developmental study of fragile X syndrome using human embryonic stem cells derived from preimplantation genetically diagnosed embryos
Eiges R et al. Developmental study of fragile X syndrome using human embryonic stem cells derived from preimplantation genetically diagnosed embryos. . 2007-11-00. Pubmed ID: 18371394; DOI: 10.1016/j.stem.2007.09.001 HUJIe001-A 2007-11-00 2007-11-00 PubMed: 18371394 DOI: 10.1016/j.stem.2007.09.001Associated cell lines:
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Bettiol E, Sartiani L, Chicha L, Krause KH, Cerbai E, Jaconi ME
Fetal bovine serum enables cardiac differentiation of human embryonic stem cells
Bettiol E et al. Fetal bovine serum enables cardiac differentiation of human embryonic stem cells. . 2007-10-00. Pubmed ID: 17459089; DOI: 10.1111/j.1432-0436.2007.00174.x WAe001-A 2007-10-00 2007-10-00 PubMed: 17459089 DOI: 10.1111/j.1432-0436.2007.00174.xAssociated cell lines:
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Ek M, Söderdahl T, Küppers-Munther B, Edsbagge J, Andersson TB, Björquist P, Cotgreave I, Jernström B, Ingelman-Sundberg M, Johansson I
Expression of drug metabolizing enzymes in hepatocyte-like cells derived from human embryonic stem cells
Ek M et al. Expression of drug metabolizing enzymes in hepatocyte-like cells derived from human embryonic stem cells. . 2007-08-01. Pubmed ID: 17568565; DOI: 10.1016/j.bcp.2007.05.009 CEBe034-A-1CEBe014-A 2007-08-01 2007-08-01 PubMed: 17568565 DOI: 10.1016/j.bcp.2007.05.009Associated cell lines:
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Söderdahl T, Küppers-Munther B, Heins N, Edsbagge J, Björquist P, Cotgreave I, Jernström B
Glutathione transferases in hepatocyte-like cells derived from human embryonic stem cells
Söderdahl T et al. Glutathione transferases in hepatocyte-like cells derived from human embryonic stem cells. . 2007-08-00. Pubmed ID: 17346923; DOI: 10.1016/j.tiv.2007.01.021 CEBe034-A-1CEBe002-ACEBe012-ACEBe014-A 2007-08-00 2007-08-00 PubMed: 17346923 DOI: 10.1016/j.tiv.2007.01.021Associated cell lines:
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Ellerström C, Strehl R, Noaksson K, Hyllner J, Semb H
Facilitated expansion of human embryonic stem cells by single-cell enzymatic dissociation
Ellerström C et al. Facilitated expansion of human embryonic stem cells by single-cell enzymatic dissociation. . 2007-07-00. Pubmed ID: 17379766; DOI: 10.1634/stemcells.2006-0607 CEBe034-A-1CEBe012-ACEBe014-A 2007-07-00 2007-07-00 PubMed: 17379766 DOI: 10.1634/stemcells.2006-0607Associated cell lines:
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International Stem Cell Initiative, Adewumi O, Aflatoonian B, Ahrlund-Richter L, Amit M, Andrews PW, Beighton G, Bello PA, Benvenisty N, Berry LS, Bevan S, Blum B, Brooking J, Chen KG, Choo AB, Churchill GA, Corbel M, Damjanov I, Draper JS, Dvorak P, Emanuelsson K, Fleck RA, Ford A, Gertow K, Gertsenstein M, Gokhale PJ, Hamilton RS, Hampl A, Healy LE, Hovatta O, Hyllner J, Imreh MP, Itskovitz-Eldor J, Jackson J, Johnson JL, Jones M, Kee K, King BL, Knowles BB, Lako M, Lebrin F, Mallon BS, Manning D, Mayshar Y, McKay RD, Michalska AE, Mikkola M, Mileikovsky M, Minger SL, Moore HD, Mummery CL, Nagy A, Nakatsuji N, O'Brien CM, Oh SK, Olsson C, Otonkoski T, Park KY, Passier R, Patel H, Patel M, Pedersen R, Pera MF, Piekarczyk MS, Pera RA, Reubinoff BE, Robins AJ, Rossant J, Rugg-Gunn P, Schulz TC, Semb H, Sherrer ES, Siemen H, Stacey GN, Stojkovic M, Suemori H, Szatkiewicz J, Turetsky T, Tuuri T, van den Brink S, Vintersten K, Vuoristo S, Ward D, Weaver TA, Young LA, Zhang W
Characterization of human embryonic stem cell lines by the International Stem Cell Initiative
International Stem Cell Initiative et al. Characterization of human embryonic stem cell lines by the International Stem Cell Initiative. . 2007-07-00. Pubmed ID: 17572666; DOI: 10.1038/nbt1318 KIe001-AKIe007-ALUMCe001-AMUNIe003-AMUNIe005-AMUNIe007-AUHe001-AUHe002-AUHe003-AUHe004-ATECHe001-ATECHe003-AAXORe001-AAXORe002-AUOSe003-AKCLe003-AHVRDe001-AHVRDe002-AHVRDe003-AHVRDe004-AHVRDe005-AHVRDe006-AHVRDe007-AHVRDe008-AHVRDe009-AHVRDe010-AHVRDe011-AHVRDe012-AHVRDe013-AHVRDe014-AHVRDe015-AHVRDe016-AHVRDe017-ASCSe001-ASCSe002-AWAe001-AWAe007-AWAe009-AWAe013-AWAe014-AVIACe001-AVIACe002-AVIACe003-AESIBIe001-AESIBIe002-AESIBIe003-AESIBIe004-AESIBIe005-AKUIMSe001-AKUIMSe002-AKUIMSe003-AMSHRIe001-AMSHRIe002-ACEBe033-ACEBe034-AUNEWe001-A 2007-07-00 2007-07-00 PubMed: 17572666 DOI: 10.1038/nbt1318 -
Laursen SB, Møllgård K, Olesen C, Oliveri RS, Brøchner CB, Byskov AG, Andersen AN, Høyer PE, Tommerup N, Yding Andersen C
Regional differences in expression of specific markers for human embryonic stem cells
Laursen SB et al. Regional differences in expression of specific markers for human embryonic stem cells. . 2007-07-00. Pubmed ID: 17623545; DOI: 10.1016/s1472-6483(10)60697-9 KUe001-AKUe002-AKUe003-AKUe004-A 2007-07-00 2007-07-00 PubMed: 17623545 DOI: 10.1016/s1472-6483(10)60697-9 -
Liao L, Li L, Zhao RC
Stem cell research in China
Liao L et al. Stem cell research in China. . 2007-06-29. Pubmed ID: 17341453; DOI: 10.1098/rstb.2007.2037; PMC: PMC2435574 SYSUe004-ASYSUe005-ASYSUe006-A 2007-06-29 2007-06-29 PubMed: 17341453 DOI: 10.1098/rstb.2007.2037Associated cell lines:
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Allegrucci C, Wu YZ, Thurston A, Denning CN, Priddle H, Mummery CL, Ward-van Oostwaard D, Andrews PW, Stojkovic M, Smith N, Parkin T, Jones ME, Warren G, Yu L, Brena RM, Plass C, Young LE
Restriction landmark genome scanning identifies culture-induced DNA methylation instability in the human embryonic stem cell epigenome
Allegrucci C et al. Restriction landmark genome scanning identifies culture-induced DNA methylation instability in the human embryonic stem cell epigenome. . 2007-05-15. Pubmed ID: 17409196; DOI: 10.1093/hmg/ddm074 UNOTe001-AUNOTe002-A 2007-05-15 2007-05-15 PubMed: 17409196 DOI: 10.1093/hmg/ddm074Associated cell lines:
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Sartiani L, Bettiol E, Stillitano F, Mugelli A, Cerbai E, Jaconi ME
Developmental changes in cardiomyocytes differentiated from human embryonic stem cells: a molecular and electrophysiological approach
Sartiani L et al. Developmental changes in cardiomyocytes differentiated from human embryonic stem cells: a molecular and electrophysiological approach. . 2007-05-00. Pubmed ID: 17255522; DOI: 10.1634/stemcells.2006-0466 WAe001-A 2007-05-00 2007-05-00 PubMed: 17255522 DOI: 10.1634/stemcells.2006-0466Associated cell lines:
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Rajala K, Hakala H, Panula S, Aivio S, Pihlajamäki H, Suuronen R, Hovatta O, Skottman H
Testing of nine different xeno-free culture media for human embryonic stem cell cultures
Rajala K et al. Testing of nine different xeno-free culture media for human embryonic stem cell cultures. . 2007-05-00. Pubmed ID: 17251355; DOI: 10.1093/humrep/del523 KIe001-AKIe004-AKIe005-AKIe006-A 2007-05-00 2007-05-00 PubMed: 17251355 DOI: 10.1093/humrep/del523 -
Narkilahti S, Rajala K, Pihlajamäki H, Suuronen R, Hovatta O, Skottman H
Monitoring and analysis of dynamic growth of human embryonic stem cells: comparison of automated instrumentation and conventional culturing methods
Narkilahti S et al. Monitoring and analysis of dynamic growth of human embryonic stem cells: comparison of automated instrumentation and conventional culturing methods. . 2007-04-12. Pubmed ID: 17428350; DOI: 10.1186/1475-925x-6-11; PMC: PMC1854905 KIe004-AKIe005-A 2007-04-12 2007-04-12 PubMed: 17428350 DOI: 10.1186/1475-925x-6-11 -
Huang G, Li WQ, Chen R, Chen ZG, Zhang XM, Mao FX, Huang SL, Li SN, Lahn BT, Xiang AP
Establishment and characterization of two new human embryonic stem cell lines, SYSU-1 and SYSU-2
Huang G et al. Establishment and characterization of two new human embryonic stem cell lines, SYSU-1 and SYSU-2. . 2007-04-05. Pubmed ID: 17442208 SYSUe001-ASYSUe002-A 2007-04-05 2007-04-05 PubMed: 17442208Associated cell lines:
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van Harmelen V, Aström G, Strömberg A, Sjölin E, Dicker A, Hovatta O, Rydén M
Differential lipolytic regulation in human embryonic stem cell-derived adipocytes
van Harmelen V et al. Differential lipolytic regulation in human embryonic stem cell-derived adipocytes. . 2007-04-00. Pubmed ID: 17426319; DOI: 10.1038/oby.2007.595 KIe006-AKIe007-A 2007-04-00 2007-04-00 PubMed: 17426319 DOI: 10.1038/oby.2007.595 -
Assou S, Le Carrour T, Tondeur S, Ström S, Gabelle A, Marty S, Nadal L, Pantesco V, Réme T, Hugnot JP, Gasca S, Hovatta O, Hamamah S, Klein B, De Vos J
A meta-analysis of human embryonic stem cells transcriptome integrated into a web-based expression atlas
Assou S et al. A meta-analysis of human embryonic stem cells transcriptome integrated into a web-based expression atlas. . 2007-04-00. Pubmed ID: 17204602; DOI: 10.1634/stemcells.2006-0352; PMC: PMC1906587 KIe003-AKIe005-A 2007-04-00 2007-04-00 PubMed: 17204602 DOI: 10.1634/stemcells.2006-0352 -
Burridge PW, Anderson D, Priddle H, Barbadillo Muñoz MD, Chamberlain S, Allegrucci C, Young LE, Denning C
Improved human embryonic stem cell embryoid body homogeneity and cardiomyocyte differentiation from a novel V-96 plate aggregation system highlights interline variability
Burridge PW et al. Improved human embryonic stem cell embryoid body homogeneity and cardiomyocyte differentiation from a novel V-96 plate aggregation system highlights interline variability. . 2007-04-00. Pubmed ID: 17185609; DOI: 10.1634/stemcells.2006-0598 UNOTe001-AUNOTe002-A 2007-04-00 2007-04-00 PubMed: 17185609 DOI: 10.1634/stemcells.2006-0598Associated cell lines:
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Kim SE, Kim BK, Gil JE, Kim SK, Kim JH
Comparative analysis of the developmental competence of three human embryonic stem cell lines in vitro
Kim SE et al. Comparative analysis of the developmental competence of three human embryonic stem cell lines in vitro. . 2007-02-28. Pubmed ID: 17464211 MIZMe007-AMIZMe008-AMIZMe009-A 2007-02-28 2007-02-28 PubMed: 17464211Associated cell lines:
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Zhang P, Kerkelä E, Skottman H, Levkov L, Kivinen K, Lahesmaa R, Hovatta O, Kere J
Distinct sets of developmentally regulated genes that are expressed by human oocytes and human embryonic stem cells
Zhang P et al. Distinct sets of developmentally regulated genes that are expressed by human oocytes and human embryonic stem cells. . 2007-03-00. Pubmed ID: 17126334; DOI: 10.1016/j.fertnstert.2006.07.1509 KIe004-A 2007-03-00 2007-03-00 PubMed: 17126334 DOI: 10.1016/j.fertnstert.2006.07.1509Associated cell lines:
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Nat R, Nilbratt M, Narkilahti S, Winblad B, Hovatta O, Nordberg A
Neurogenic neuroepithelial and radial glial cells generated from six human embryonic stem cell lines in serum-free suspension and adherent cultures
Nat R et al. Neurogenic neuroepithelial and radial glial cells generated from six human embryonic stem cell lines in serum-free suspension and adherent cultures. . 2007-03-00. Pubmed ID: 17152062; DOI: 10.1002/glia.20463 KIe001-AKIe004-AKIe005-AKIe006-AKIe007-AKIe017-A 2007-03-00 2007-03-00 PubMed: 17152062 DOI: 10.1002/glia.20463 -
Chen HF, Kuo HC, Chien CL, Shun CT, Yao YL, Ip PL, Chuang CY, Wang CC, Yang YS, Ho HN
Derivation, characterization and differentiation of human embryonic stem cells: comparing serum-containing versus serum-free media and evidence of germ cell differentiation
Chen HF et al. Derivation, characterization and differentiation of human embryonic stem cells: comparing serum-containing versus serum-free media and evidence of germ cell differentiation. . 2007-02-00. Pubmed ID: 17071820; DOI: 10.1093/humrep/del412 NTUe001-ANTUe002-ANTUe003-A 2007-02-00 2007-02-00 PubMed: 17071820 DOI: 10.1093/humrep/del412 -
Synnergren J, Giesler TL, Adak S, Tandon R, Noaksson K, Lindahl A, Nilsson P, Nelson D, Olsson B, Englund MC, Abbot S, Sartipy P
Differentiating human embryonic stem cells express a unique housekeeping gene signature
Synnergren J et al. Differentiating human embryonic stem cells express a unique housekeeping gene signature. . 2007-02-00. Pubmed ID: 17284652; DOI: 10.1634/stemcells.2006-0247 CEBe034-A-1 2007-02-00 2007-02-00 PubMed: 17284652 DOI: 10.1634/stemcells.2006-0247Associated cell lines:
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Baker DE, Harrison NJ, Maltby E, Smith K, Moore HD, Shaw PJ, Heath PR, Holden H, Andrews PW
Adaptation to culture of human embryonic stem cells and oncogenesis in vivo
Baker DE et al. Adaptation to culture of human embryonic stem cells and oncogenesis in vivo. . 2007-02-00. Pubmed ID: 17287758; DOI: 10.1038/nbt1285 AXORe001-AAXORe004-AAXORe005-AHVRDe005-AHVRDe006-AHVRDe007-AHVRDe010-AHVRDe013-AHVRDe014-AHVRDe017-AWAe001-AWAe007-AWAe014-A 2007-02-00 2007-02-00 PubMed: 17287758 DOI: 10.1038/nbt1285Associated cell lines:
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Ullmann U, In't Veld P, Gilles C, Sermon K, De Rycke M, Van de Velde H, Van Steirteghem A, Liebaers I
Epithelial-mesenchymal transition process in human embryonic stem cells cultured in feeder-free conditions
Ullmann U et al. Epithelial-mesenchymal transition process in human embryonic stem cells cultured in feeder-free conditions. . 2007-01-00. Pubmed ID: 17090644; DOI: 10.1093/molehr/gal091 VUBe001-A 2007-01-00 2007-01-00 PubMed: 17090644 DOI: 10.1093/molehr/gal091Associated cell lines:
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Hasegawa K, Fujioka T, Nakamura Y, Nakatsuji N, Suemori H
A method for the selection of human embryonic stem cell sublines with high replating efficiency after single-cell dissociation
Hasegawa K et al. A method for the selection of human embryonic stem cell sublines with high replating efficiency after single-cell dissociation. . 2006-12-00. Pubmed ID: 16931777; DOI: 10.1634/stemcells.2005-0657 KUIMSe003-A-1 2006-12-00 2006-12-00 PubMed: 16931777 DOI: 10.1634/stemcells.2005-0657Associated cell lines:
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Valbuena D, Galán A, Sánchez E, Poo ME, Gómez E, Sánchez-Luengo S, Melguizo D, García A, Ruiz V, Moreno R, Pellicer A, Simón C
Derivation and characterization of three new Spanish human embryonic stem cell lines (VAL -3 -4 -5) on human feeder and in serum-free conditions
Valbuena D et al. Derivation and characterization of three new Spanish human embryonic stem cell lines (VAL -3 -4 -5) on human feeder and in serum-free conditions. . 2006-12-00. Pubmed ID: 17169214; DOI: 10.1016/s1472-6483(10)61038-3 ESe011-AESe012-AESe013-A 2006-12-00 2006-12-00 PubMed: 17169214 DOI: 10.1016/s1472-6483(10)61038-3 -
Zhang X, Stojkovic P, Przyborski S, Cooke M, Armstrong L, Lako M, Stojkovic M
Derivation of human embryonic stem cells from developing and arrested embryos
Zhang X et al. Derivation of human embryonic stem cells from developing and arrested embryos. . 2006-12-00. Pubmed ID: 16990582; DOI: 10.1634/stemcells.2006-0377 UNEWe006-AUNEWe007-AUNEWe008-AUNEWe009-A 2006-12-00 2006-12-00 PubMed: 16990582 DOI: 10.1634/stemcells.2006-0377Associated cell lines:
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Norström A, Akesson K, Hardarson T, Hamberger L, Björquist P, Sartipy P
Molecular and pharmacological properties of human embryonic stem cell-derived cardiomyocytes
Norström A et al. Molecular and pharmacological properties of human embryonic stem cell-derived cardiomyocytes. . 2006-12-00. Pubmed ID: 17138763; DOI: 10.1177/153537020623101113 CEBe012-A 2006-12-00 2006-12-00 PubMed: 17138763 DOI: 10.1177/153537020623101113Associated cell lines:
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Hirst M, Delaney A, Rogers SA, Schnerch A, Persaud DR, O'Connor MD, Zeng T, Moksa M, Fichter K, Mah D, Go A, Morin RD, Baross A, Zhao Y, Khattra J, Prabhu AL, Pandoh P, McDonald H, Asano J, Dhalla N, Ma K, Lee S, Ally A, Chahal N, Menzies S, Siddiqui A, Holt R, Jones S, Gerhard DS, Thomson JA, Eaves CJ, Marra MA
LongSAGE profiling of nine human embryonic stem cell lines
Hirst M et al. LongSAGE profiling of nine human embryonic stem cell lines. . 2007-00-00. Pubmed ID: 17570852; DOI: 10.1186/gb-2007-8-6-r113; PMC: PMC2394759 WAe001-AWAe007-AWAe009-AWAe013-AWAe014-AVIACe001-AESIBIe003-AESIBIe004-AUCSFe002-A 2007-00-00 2007-00-00 PubMed: 17570852 DOI: 10.1186/gb-2007-8-6-r113Associated cell lines:
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Klimanskaya I, Chung Y, Becker S, Lu SJ, Lanza R
Human embryonic stem cell lines derived from single blastomeres
Klimanskaya I et al. Human embryonic stem cell lines derived from single blastomeres. . 2006-11-23. Pubmed ID: 16929302; DOI: 10.1038/nature05142 ACTe001-AACTe002-A 2006-11-23 2006-11-23 PubMed: 16929302 DOI: 10.1038/nature05142 -
Trivedi HL, Mishra VV, Vanikar AV, Modi PR, Shah VR, Shah PR, Firoz A
Embryonic stem cell derived and adult hematopoietic stem cell transplantation for tolerance induction in a renal allograft recipient:--a case report
Trivedi HL et al. Embryonic stem cell derived and adult hematopoietic stem cell transplantation for tolerance induction in a renal allograft recipient:--a case report. . 2006-11-00. Pubmed ID: 17112910; DOI: 10.1016/j.transproceed.2006.08.173 ITSe001-A 2006-11-00 2006-11-00 PubMed: 17112910 DOI: 10.1016/j.transproceed.2006.08.173Associated cell lines:
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Grinnemo KH, Kumagai-Braesch M, Månsson-Broberg A, Skottman H, Hao X, Siddiqui A, Andersson A, Strömberg AM, Lahesmaa R, Hovatta O, Sylven C, Corbascio M, Dellgren G
Human embryonic stem cells are immunogenic in allogeneic and xenogeneic settings
Grinnemo KH et al. Human embryonic stem cells are immunogenic in allogeneic and xenogeneic settings. . 2006-11-00. Pubmed ID: 17169186; DOI: 10.1016/s1472-6483(10)60663-3 KIe004-AKIe005-AKIe006-AKIe007-AKIe011-AKIe012-AKIe015-A 2006-11-00 2006-11-00 PubMed: 17169186 DOI: 10.1016/s1472-6483(10)60663-3 -
D'Amour KA, Bang AG, Eliazer S, Kelly OG, Agulnick AD, Smart NG, Moorman MA, Kroon E, Carpenter MK, Baetge EE
Production of pancreatic hormone-expressing endocrine cells from human embryonic stem cells
D'Amour KA et al. Production of pancreatic hormone-expressing endocrine cells from human embryonic stem cells. . 2006-11-00. Pubmed ID: 17053790; DOI: 10.1038/nbt1259 VIACe005-A 2006-11-00 2006-11-00 PubMed: 17053790 DOI: 10.1038/nbt1259Associated cell lines:
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Aghajanova L, Skottman H, Strömberg AM, Inzunza J, Lahesmaa R, Hovatta O
Expression of leukemia inhibitory factor and its receptors is increased during differentiation of human embryonic stem cells
Aghajanova L et al. Expression of leukemia inhibitory factor and its receptors is increased during differentiation of human embryonic stem cells. . 2006-10-00. Pubmed ID: 16949591; DOI: 10.1016/j.fertnstert.2005.12.081 KIe001-AKIe003-AKIe004-AKIe005-A 2006-10-00 2006-10-00 PubMed: 16949591 DOI: 10.1016/j.fertnstert.2005.12.081 -
Ellerström C, Strehl R, Moya K, Andersson K, Bergh C, Lundin K, Hyllner J, Semb H
Derivation of a xeno-free human embryonic stem cell line
Ellerström C et al. Derivation of a xeno-free human embryonic stem cell line. . 2006-10-00. Pubmed ID: 16741223; DOI: 10.1634/stemcells.2006-0130 CEBe012-ACEBe032-A 2006-10-00 2006-10-00 PubMed: 16741223 DOI: 10.1634/stemcells.2006-0130 -
Bibikova M, Chudin E, Wu B, Zhou L, Garcia EW, Liu Y, Shin S, Plaia TW, Auerbach JM, Arking DE, Gonzalez R, Crook J, Davidson B, Schulz TC, Robins A, Khanna A, Sartipy P, Hyllner J, Vanguri P, Savant-Bhonsale S, Smith AK, Chakravarti A, Maitra A, Rao M, Barker DL, Loring JF, Fan JB
Human embryonic stem cells have a unique epigenetic signature
Bibikova M et al. Human embryonic stem cells have a unique epigenetic signature. . 2006-09-00. Pubmed ID: 16899657; DOI: 10.1101/gr.5319906; PMC: PMC1557765 CEBe034-A-1 2006-09-00 2006-09-00 PubMed: 16899657 DOI: 10.1101/gr.5319906Associated cell lines:
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Josephson R, Sykes G, Liu Y, Ording C, Xu W, Zeng X, Shin S, Loring J, Maitra A, Rao MS, Auerbach JM
A molecular scheme for improved characterization of human embryonic stem cell lines
Josephson R et al. A molecular scheme for improved characterization of human embryonic stem cell lines. . 2006-08-18. Pubmed ID: 16919167; DOI: 10.1186/1741-7007-4-28; PMC: PMC1601965 CEBe034-A-1TECHe001-ATECHe002-ATECHe003-AHVRDe007-AWAe001-AWAe007-AWAe009-AVIACe001-AVIACe002-AVIACe003-AESIBIe002-AESIBIe003-ACEBe033-ACEBe034-AVIACe001-A-2DALCe001-A 2006-08-18 2006-08-18 PubMed: 16919167 DOI: 10.1186/1741-7007-4-28 -
Mikkola M, Olsson C, Palgi J, Ustinov J, Palomaki T, Horelli-Kuitunen N, Knuutila S, Lundin K, Otonkoski T, Tuuri T
Distinct differentiation characteristics of individual human embryonic stem cell lines
Mikkola M et al. Distinct differentiation characteristics of individual human embryonic stem cell lines. . 2006-08-08. Pubmed ID: 16895598; DOI: 10.1186/1471-213x-6-40; PMC: PMC1557488 UHe001-AUHe002-AUHe003-AUHe004-AUHe005-A 2006-08-08 2006-08-08 PubMed: 16895598 DOI: 10.1186/1471-213x-6-40 -
Li SS, Liu YH, Tseng CN, Chung TL, Lee TY, Singh S
Characterization and gene expression profiling of five new human embryonic stem cell lines derived in Taiwan
Li SS et al. Characterization and gene expression profiling of five new human embryonic stem cell lines derived in Taiwan. . 2006-08-00. Pubmed ID: 16978057; DOI: 10.1089/scd.2006.15.532 KMUe001-AKMUe002-AKMUe003-AKMUe004-AKMUe005-A 2006-08-00 2006-08-00 PubMed: 16978057 DOI: 10.1089/scd.2006.15.532 -
Suemori H, Yasuchika K, Hasegawa K, Fujioka T, Tsuneyoshi N, Nakatsuji N
Efficient establishment of human embryonic stem cell lines and long-term maintenance with stable karyotype by enzymatic bulk passage
Suemori H et al. Efficient establishment of human embryonic stem cell lines and long-term maintenance with stable karyotype by enzymatic bulk passage. . 2006-07-07. Pubmed ID: 16707099; DOI: 10.1016/j.bbrc.2006.04.135 KUIMSe001-AKUIMSe002-AKUIMSe003-A 2006-07-07 2006-07-07 PubMed: 16707099 DOI: 10.1016/j.bbrc.2006.04.135Associated cell lines:
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James D, Noggle SA, Swigut T, Brivanlou AH
Contribution of human embryonic stem cells to mouse blastocysts
James D et al. Contribution of human embryonic stem cells to mouse blastocysts. . 2006-07-01. Pubmed ID: 16769046; DOI: 10.1016/j.ydbio.2006.03.026 RUESe001-A 2006-07-01 2006-07-01 PubMed: 16769046 DOI: 10.1016/j.ydbio.2006.03.026Associated cell lines:
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Heins N, Lindahl A, Karlsson U, Rehnström M, Caisander G, Emanuelsson K, Hanson C, Semb H, Björquist P, Sartipy P, Hyllner J
Clonal derivation and characterization of human embryonic stem cell lines
Heins N et al. Clonal derivation and characterization of human embryonic stem cell lines. . 2006-04-20. Pubmed ID: 16324761; DOI: 10.1016/j.jbiotec.2005.10.010 CEBe034-A-1CEBe002-A-3 2006-04-20 2006-04-20 PubMed: 16324761 DOI: 10.1016/j.jbiotec.2005.10.010Associated cell lines:
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Plaia TW, Josephson R, Liu Y, Zeng X, Ording C, Toumadje A, Brimble SN, Sherrer ES, Uhl EW, Freed WJ, Schulz TC, Maitra A, Rao MS, Auerbach JM
Characterization of a new NIH-registered variant human embryonic stem cell line, BG01V: a tool for human embryonic stem cell research
Plaia TW et al. Characterization of a new NIH-registered variant human embryonic stem cell line, BG01V: a tool for human embryonic stem cell research. . 2006-03-00. Pubmed ID: 16293579; DOI: 10.1634/stemcells.2005-0315 VIACe001-A-2 2006-03-00 2006-03-00 PubMed: 16293579 DOI: 10.1634/stemcells.2005-0315Associated cell lines:
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Mandal A, Tipnis S, Pal R, Ravindran G, Bose B, Patki A, Rao MS, Khanna A
Characterization and in vitro differentiation potential of a new human embryonic stem cell line, ReliCellhES1
Mandal A et al. Characterization and in vitro differentiation potential of a new human embryonic stem cell line, ReliCellhES1. . 2006-03-00. Pubmed ID: 16533307; DOI: 10.1111/j.1432-0436.2006.00051.x DALCe001-A 2006-03-00 2006-03-00 PubMed: 16533307 DOI: 10.1111/j.1432-0436.2006.00051.xAssociated cell lines:
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Baharvand H, Ashtiani SK, Taee A, Massumi M, Valojerdi MR, Yazdi PE, Moradi SZ, Farrokhi A
Generation of new human embryonic stem cell lines with diploid and triploid karyotypes
Baharvand H et al. Generation of new human embryonic stem cell lines with diploid and triploid karyotypes. . 2006-02-00. Pubmed ID: 16512855; DOI: 10.1111/j.1440-169x.2006.00851.x RIe002-ARIe003-ARIe004-ARIe005-ARIe006-A 2006-02-00 2006-02-00 PubMed: 16512855 DOI: 10.1111/j.1440-169x.2006.00851.x -
Mateizel I, De Temmerman N, Ullmann U, Cauffman G, Sermon K, Van de Velde H, De Rycke M, Degreef E, Devroey P, Liebaers I, Van Steirteghem A
Derivation of human embryonic stem cell lines from embryos obtained after IVF and after PGD for monogenic disorders
Mateizel I et al. Derivation of human embryonic stem cell lines from embryos obtained after IVF and after PGD for monogenic disorders. . 2006-02-00. Pubmed ID: 16284066; DOI: 10.1093/humrep/dei345 VUBe001-AVUBe002-AVUBe003-AVUBe004-AVUBe005-A 2006-02-00 2006-02-00 PubMed: 16284066 DOI: 10.1093/humrep/dei345 -
Ludwig TE, Levenstein ME, Jones JM, Berggren WT, Mitchen ER, Frane JL, Crandall LJ, Daigh CA, Conard KR, Piekarczyk MS, Llanas RA, Thomson JA
Derivation of human embryonic stem cells in defined conditions
Ludwig TE et al. Derivation of human embryonic stem cells in defined conditions. . 2006-02-00. Pubmed ID: 16388305; DOI: 10.1038/nbt1177 WAe001-AWAe007-AWAe009-AWAe014-AWISCe001-AWISCe002-A 2006-02-00 2006-02-00 PubMed: 16388305 DOI: 10.1038/nbt1177Associated cell lines:
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Sidhu KS, Tuch BE
Derivation of three clones from human embryonic stem cell lines by FACS sorting and their characterization
Sidhu KS et al. Derivation of three clones from human embryonic stem cell lines by FACS sorting and their characterization. . 2006-02-00. Pubmed ID: 16522163; DOI: 10.1089/scd.2006.15.61 ESIBIe003-A-1ESIBIe003-A-2ESIBIe003-A-3 2006-02-00 2006-02-00 PubMed: 16522163 DOI: 10.1089/scd.2006.15.61Associated cell lines:
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Sun BW, Yang AC, Feng Y, Sun YJ, Zhu Yf, Zhang Y, Jiang H, Li CL, Gao FR, Zhang ZH, Wang WC, Kong XY, Jin G, Fu SJ, Jin Y
Temporal and parental-specific expression of imprinted genes in a newly derived Chinese human embryonic stem cell line and embryoid bodies
Sun BW et al. Temporal and parental-specific expression of imprinted genes in a newly derived Chinese human embryonic stem cell line and embryoid bodies. . 2006-01-01. Pubmed ID: 16319131; DOI: 10.1093/hmg/ddi427 SJTUe001-A 2006-01-01 2006-01-01 PubMed: 16319131 DOI: 10.1093/hmg/ddi427Associated cell lines:
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Lysdahl H, Gabrielsen A, Minger SL, Patel MJ, Fink T, Petersen K, Ebbesen P, Zachar V
Derivation and characterization of four new human embryonic stem cell lines: the Danish experience
Lysdahl H et al. Derivation and characterization of four new human embryonic stem cell lines: the Danish experience. . 2006-01-00. Pubmed ID: 16454946; DOI: 10.1016/s1472-6483(10)60990-x AAUe001-AAAUe002-AAAUe003-AAAUe004-A 2006-01-00 2006-01-00 PubMed: 16454946 DOI: 10.1016/s1472-6483(10)60990-x -
Skottman H, Strömberg AM, Matilainen E, Inzunza J, Hovatta O, Lahesmaa R
Unique gene expression signature by human embryonic stem cells cultured under serum-free conditions correlates with their enhanced and prolonged growth in an undifferentiated stage
Skottman H et al. Unique gene expression signature by human embryonic stem cells cultured under serum-free conditions correlates with their enhanced and prolonged growth in an undifferentiated stage. . 2006-01-00. Pubmed ID: 16100004; DOI: 10.1634/stemcells.2004-0189 KIe001-AKIe003-AKIe004-A 2006-01-00 2006-01-00 PubMed: 16100004 DOI: 10.1634/stemcells.2004-0189 -
Hong-mei P, Gui-an C
Serum-free medium cultivation to improve efficacy in establishment of human embryonic stem cell lines
Hong-mei P et al. Serum-free medium cultivation to improve efficacy in establishment of human embryonic stem cell lines. . 2006-01-00. Pubmed ID: 16143641; DOI: 10.1093/humrep/dei275 BJMUe001-ABJMUe002-ABJMUe003-ABJMUe004-A 2006-01-00 2006-01-00 PubMed: 16143641 DOI: 10.1093/humrep/dei275Associated cell lines:
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Muotri AR, Nakashima K, Toni N, Sandler VM, Gage FH
Development of functional human embryonic stem cell-derived neurons in mouse brain
Muotri AR et al. Development of functional human embryonic stem cell-derived neurons in mouse brain. . 2005-12-20. Pubmed ID: 16352714; DOI: 10.1073/pnas.0509315102; PMC: PMC1317971 SALKe001-A 2005-12-20 2005-12-20 PubMed: 16352714 DOI: 10.1073/pnas.0509315102Associated cell lines:
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Caisander G, Park H, Frej K, Lindqvist J, Bergh C, Lundin K, Hanson C
Chromosomal integrity maintained in five human embryonic stem cell lines after prolonged in vitro culture
Caisander G et al. Chromosomal integrity maintained in five human embryonic stem cell lines after prolonged in vitro culture. . 2006-00-00. Pubmed ID: 16544187; DOI: 10.1007/s10577-006-1019-8 CEBe034-A-1CEBe012-ACEBe027-ACEBe002-A-3 2006-00-00 2006-00-00 PubMed: 16544187 DOI: 10.1007/s10577-006-1019-8Associated cell lines:
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Fletcher JM, Ferrier PM, Gardner JO, Harkness L, Dhanjal S, Serhal P, Harper J, Delhanty J, Brownstein DG, Prasad YR, Lebkowski J, Mandalam R, Wilmut I, De Sousa PA
Variations in humanized and defined culture conditions supporting derivation of new human embryonic stem cell lines
Fletcher JM et al. Variations in humanized and defined culture conditions supporting derivation of new human embryonic stem cell lines. . 2006-00-00. Pubmed ID: 17196096; DOI: 10.1089/clo.2006.8.319 EDe001-AEDe002-AEDe003-AEDe004-AEDe005-AEDe006-A 2006-00-00 2006-00-00 PubMed: 17196096 DOI: 10.1089/clo.2006.8.319 -
Noaksson K, Zoric N, Zeng X, Rao MS, Hyllner J, Semb H, Kubista M, Sartipy P
Monitoring differentiation of human embryonic stem cells using real-time PCR
Noaksson K et al. Monitoring differentiation of human embryonic stem cells using real-time PCR. . 2005-11-00. Pubmed ID: 16081663; DOI: 10.1634/stemcells.2005-0093 CEBe002-ACEBe012-ACEBe015-ACEBe018-ACEBe002-A-1 2005-11-00 2005-11-00 PubMed: 16081663 DOI: 10.1634/stemcells.2005-0093Associated cell lines:
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Maitra A, Arking DE, Shivapurkar N, Ikeda M, Stastny V, Kassauei K, Sui G, Cutler DJ, Liu Y, Brimble SN, Noaksson K, Hyllner J, Schulz TC, Zeng X, Freed WJ, Crook J, Abraham S, Colman A, Sartipy P, Matsui S, Carpenter M, Gazdar AF, Rao M, Chakravarti A
Genomic alterations in cultured human embryonic stem cells
Maitra A et al. Genomic alterations in cultured human embryonic stem cells. . 2005-10-00. Pubmed ID: 16142235; DOI: 10.1038/ng1631 CEBe034-A-1 2005-10-00 2005-10-00 PubMed: 16142235 DOI: 10.1038/ng1631Associated cell lines:
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van de Stolpe A, van den Brink S, van Rooijen M, Ward-van Oostwaard D, van Inzen W, Slaper-Cortenbach I, Fauser B, van den Hout N, Weima S, Passier R, Smith N, Denning C, Mummery C
Human embryonic stem cells: towards therapies for cardiac disease. Derivation of a Dutch human embryonic stem cell line
van de Stolpe A et al. Human embryonic stem cells: towards therapies for cardiac disease. Derivation of a Dutch human embryonic stem cell line. . 2005-10-00. Pubmed ID: 16274613; DOI: 10.1016/s1472-6483(10)61144-3 LUMCe001-ALUMCe002-ALUMCe003-ALUMCe004-A 2005-10-00 2005-10-00 PubMed: 16274613 DOI: 10.1016/s1472-6483(10)61144-3Associated cell lines:
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Skottman H, Mikkola M, Lundin K, Olsson C, Strömberg AM, Tuuri T, Otonkoski T, Hovatta O, Lahesmaa R
Gene expression signatures of seven individual human embryonic stem cell lines
Skottman H et al. Gene expression signatures of seven individual human embryonic stem cell lines. . 2005-10-00. Pubmed ID: 16081666; DOI: 10.1634/stemcells.2004-0341 KIe001-AKIe003-AKIe004-A 2005-10-00 2005-10-00 PubMed: 16081666 DOI: 10.1634/stemcells.2004-0341 -
Wang Q, Fang ZF, Jin F, Lu Y, Gai H, Sheng HZ
Derivation and growing human embryonic stem cells on feeders derived from themselves
Wang Q et al. Derivation and growing human embryonic stem cells on feeders derived from themselves. . 2005-10-00. Pubmed ID: 15955827; DOI: 10.1634/stemcells.2004-0347 SSMUe001-ASSMUe002-ASSMUe003-A 2005-10-00 2005-10-00 PubMed: 15955827 DOI: 10.1634/stemcells.2004-0347Associated cell lines:
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Dvorak P, Dvorakova D, Koskova S, Vodinska M, Najvirtova M, Krekac D, Hampl A
Expression and potential role of fibroblast growth factor 2 and its receptors in human embryonic stem cells
Dvorak P et al. Expression and potential role of fibroblast growth factor 2 and its receptors in human embryonic stem cells. . 2005-09-00. Pubmed ID: 15955829; DOI: 10.1634/stemcells.2004-0303 MUNIe003-AMUNIe004-AMUNIe005-AMUNIe007-A 2005-09-00 2005-09-00 PubMed: 15955829 DOI: 10.1634/stemcells.2004-0303Associated cell lines:
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Sjögren-Jansson E, Zetterström M, Moya K, Lindqvist J, Strehl R, Eriksson PS
Large-scale propagation of four undifferentiated human embryonic stem cell lines in a feeder-free culture system
Sjögren-Jansson E et al. Large-scale propagation of four undifferentiated human embryonic stem cell lines in a feeder-free culture system. . 2005-08-00. Pubmed ID: 15965986; DOI: 10.1002/dvdy.20459 CEBe006-ACEBe012-ACEBe014-A 2005-08-00 2005-08-00 PubMed: 15965986 DOI: 10.1002/dvdy.20459 -
Klimanskaya I, Chung Y, Meisner L, Johnson J, West MD, Lanza R
Human embryonic stem cells derived without feeder cells
Klimanskaya I et al. Human embryonic stem cells derived without feeder cells. . 2005-05-07. Pubmed ID: 15885296; DOI: 10.1016/s0140-6736(05)66473-2 ACTe003-A 2005-05-07 2005-05-07 PubMed: 15885296 DOI: 10.1016/s0140-6736(05)66473-2Associated cell lines:
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Findikli N, Kahraman S, Akcin O, Sertyel S, Candan Z
Establishment and characterization of new human embryonic stem cell lines
Findikli N et al. Establishment and characterization of new human embryonic stem cell lines. . 2005-05-00. Pubmed ID: 15949219; DOI: 10.1016/s1472-6483(10)61669-0 IMHe001-A 2005-05-00 2005-05-00 PubMed: 15949219 DOI: 10.1016/s1472-6483(10)61669-0Associated cell lines:
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Fang ZF, Jin F, Gai H, Chen Y, Wu L, Liu AL, Chen B, Sheng HZ
Human embryonic stem cell lines derived from the Chinese population
Fang ZF et al. Human embryonic stem cell lines derived from the Chinese population. . 2005-05-00. Pubmed ID: 15916726; DOI: 10.1038/sj.cr.7290307 SSMUe004-ASSMUe005-ASSMUe006-ASSMUe008-ASSMUe009-ASSMUe010-A 2005-05-00 2005-05-00 PubMed: 15916726 DOI: 10.1038/sj.cr.7290307Associated cell lines:
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Inzunza J, Gertow K, Strömberg MA, Matilainen E, Blennow E, Skottman H, Wolbank S, Ahrlund-Richter L, Hovatta O
Derivation of human embryonic stem cell lines in serum replacement medium using postnatal human fibroblasts as feeder cells
Inzunza J et al. Derivation of human embryonic stem cell lines in serum replacement medium using postnatal human fibroblasts as feeder cells. . 2005-04-00. Pubmed ID: 15790775; DOI: 10.1634/stemcells.2004-0201 KIe005-AKIe006-AKIe007-AKIe008-AKIe009-AKIe010-AKIe011-AKIe012-AKIe013-AKIe014-AKIe015-AKIe030-A 2005-04-00 2005-04-00 PubMed: 15790775 DOI: 10.1634/stemcells.2004-0201 -
Costa M, Dottori M, Ng E, Hawes SM, Sourris K, Jamshidi P, Pera MF, Elefanty AG, Stanley EG
The hESC line Envy expresses high levels of GFP in all differentiated progeny
Costa M et al. The hESC line Envy expresses high levels of GFP in all differentiated progeny. . 2005-04-00. Pubmed ID: 15782217; DOI: 10.1038/nmeth748 ESIBIe003-A-4 2005-04-00 2005-04-00 PubMed: 15782217 DOI: 10.1038/nmeth748Associated cell lines:
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Darnfors C, Flodin A, Andersson K, Caisander G, Lindqvist J, Hyllner J, Wahlström J, Sartipy P
High-resolution analysis of the subtelomeric regions of human embryonic stem cells
Darnfors C et al. High-resolution analysis of the subtelomeric regions of human embryonic stem cells. . 2005-04-00. Pubmed ID: 15790769; DOI: 10.1634/stemcells.2004-0254 CEBe002-ACEBe006-ACEBe012-ACEBe015-ACEBe022-ACEBe027-ACEBe002-A-1 2005-04-00 2005-04-00 PubMed: 15790769 DOI: 10.1634/stemcells.2004-0254 -
Kim SJ, Lee JE, Park JH, Lee JB, Kim JM, Yoon BS, Song JM, Roh SI, Kim CG, Yoon HS
Efficient derivation of new human embryonic stem cell lines
Kim SJ et al. Efficient derivation of new human embryonic stem cell lines. . 2005-02-28. Pubmed ID: 15750339 MIZMe007-AMIZMe008-AMIZMe009-AMIZMe010-AMIZMe011-AMIZMe012-AMIZMe013-AMIZMe014-AMIZMe015-A 2005-02-28 2005-02-28 PubMed: 15750339Associated cell lines:
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Pickering SJ, Minger SL, Patel M, Taylor H, Black C, Burns CJ, Ekonomou A, Braude PR
Generation of a human embryonic stem cell line encoding the cystic fibrosis mutation deltaF508, using preimplantation genetic diagnosis
Pickering SJ et al. Generation of a human embryonic stem cell line encoding the cystic fibrosis mutation deltaF508, using preimplantation genetic diagnosis. . 2005-03-00. Pubmed ID: 15820050; DOI: 10.1016/s1472-6483(10)61801-9 KCLe003-A 2005-03-00 2005-03-00 PubMed: 15820050 DOI: 10.1016/s1472-6483(10)61801-9Associated cell lines:
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Oh SK, Kim HS, Ahn HJ, Seol HW, Kim YY, Park YB, Yoon CJ, Kim DW, Kim SH, Moon SY
Derivation and characterization of new human embryonic stem cell lines: SNUhES1, SNUhES2, and SNUhES3
Oh SK et al. Derivation and characterization of new human embryonic stem cell lines: SNUhES1, SNUhES2, and SNUhES3. . 2005-02-00. Pubmed ID: 15671144; DOI: 10.1634/stemcells.2004-0122 SNUe001-ASNUe002-ASNUe003-A 2005-02-00 2005-02-00 PubMed: 15671144 DOI: 10.1634/stemcells.2004-0122 -
Verlinsky Y, Strelchenko N, Kukharenko V, Rechitsky S, Verlinsky O, Galat V, Kuliev A
Human embryonic stem cell lines with genetic disorders
Verlinsky Y et al. Human embryonic stem cell lines with genetic disorders. . 2005-01-00. Pubmed ID: 15705304; DOI: 10.1016/s1472-6483(10)60810-3 RGIe040-ARGIe041-ARGIe049-ARGIe050-ARGIe051-ARGIe052-ARGIe053-ARGIe057-ARGIe061-ARGIe062-ARGIe066-ARGIe072-ARGIe077-ARGIe086-ARGIe091-ARGIe092-ARGIe098-ARGIe105-A 2005-01-00 2005-01-00 PubMed: 15705304 DOI: 10.1016/s1472-6483(10)60810-3 -
Lee JB, Lee JE, Park JH, Kim SJ, Kim MK, Roh SI, Yoon HS
Establishment and maintenance of human embryonic stem cell lines on human feeder cells derived from uterine endometrium under serum-free condition
Lee JB et al. Establishment and maintenance of human embryonic stem cell lines on human feeder cells derived from uterine endometrium under serum-free condition. . 2005-01-00. Pubmed ID: 15317691; DOI: 10.1095/biolreprod.104.033480 MIZMe004-AMIZMe005-AMIZMe006-A 2005-01-00 2005-01-00 PubMed: 15317691 DOI: 10.1095/biolreprod.104.033480Associated cell lines:
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Ren CP, Zhao M, Shan WJ, Yang XY, Yin ZH, Jiang XJ, Zhang HB, Yao KT
Establishment of human embryonic stem cell line stably expressing Epstein-Barr virus-encoded nuclear antigen 1
Ren CP et al. Establishment of human embryonic stem cell line stably expressing Epstein-Barr virus-encoded nuclear antigen 1. . 2005-01-00. Pubmed ID: 15645084; DOI: 10.1093/abbs/37.1.68 WAe009-A-10 2005-01-00 2005-01-00 PubMed: 15645084 DOI: 10.1093/abbs/37.1.68Associated cell lines:
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Brimble SN, Zeng X, Weiler DA, Luo Y, Liu Y, Lyons IG, Freed WJ, Robins AJ, Rao MS, Schulz TC
Karyotypic stability, genotyping, differentiation, feeder-free maintenance, and gene expression sampling in three human embryonic stem cell lines derived prior to August 9, 2001
Brimble SN et al. Karyotypic stability, genotyping, differentiation, feeder-free maintenance, and gene expression sampling in three human embryonic stem cell lines derived prior to August 9, 2001. . 2004-12-00. Pubmed ID: 15684826; DOI: 10.1089/scd.2004.13.585 VIACe001-AVIACe002-AVIACe003-A 2004-12-00 2004-12-00 PubMed: 15684826 DOI: 10.1089/scd.2004.13.585Associated cell lines:
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Nat R, Hovatta O
In vitro neural differentiation of human embryonic stem cells
Nat R et al. In vitro neural differentiation of human embryonic stem cells. . 2004-10-00. Pubmed ID: 15601586; DOI: 10.1111/j.1582-4934.2004.tb00482.x; PMC: PMC6740232 KIe004-A 2004-10-00 2004-10-00 PubMed: 15601586 DOI: 10.1111/j.1582-4934.2004.tb00482.xAssociated cell lines:
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Hansson M, Tonning A, Frandsen U, Petri A, Rajagopal J, Englund MC, Heller RS, Håkansson J, Fleckner J, Sköld HN, Melton D, Semb H, Serup P
Artifactual insulin release from differentiated embryonic stem cells
Hansson M et al. Artifactual insulin release from differentiated embryonic stem cells. . 2004-10-00. Pubmed ID: 15448090; DOI: 10.2337/diabetes.53.10.2603 CEBe010-A 2004-10-00 2004-10-00 PubMed: 15448090 DOI: 10.2337/diabetes.53.10.2603Associated cell lines:
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Koivisto H, Hyvärinen M, Strömberg AM, Inzunza J, Matilainen E, Mikkola M, Hovatta O, Teerijoki H
Cultures of human embryonic stem cells: serum replacement medium or serum-containing media and the effect of basic fibroblast growth factor
Koivisto H et al. Cultures of human embryonic stem cells: serum replacement medium or serum-containing media and the effect of basic fibroblast growth factor. . 2004-09-00. Pubmed ID: 15353086; DOI: 10.1016/s1472-6483(10)62150-5 KIe004-A 2004-09-00 2004-09-00 PubMed: 15353086 DOI: 10.1016/s1472-6483(10)62150-5Associated cell lines:
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Draper JS, Moore HD, Ruban LN, Gokhale PJ, Andrews PW
Culture and characterization of human embryonic stem cells
Draper JS et al. Culture and characterization of human embryonic stem cells. . 2004-08-00. Pubmed ID: 15345125; DOI: 10.1089/scd.2004.13.325 AXORe001-AWAe007-A 2004-08-00 2004-08-00 PubMed: 15345125 DOI: 10.1089/scd.2004.13.325Associated cell lines:
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Imreh MP, Wolbank S, Unger C, Gertow K, Aints A, Szeles A, Imreh S, Hovatta O, Fried G, Dilber S, Ahrlund-Richter L
Culture and expansion of the human embryonic stem cell line HS181, evaluated in a double-color system
Imreh MP et al. Culture and expansion of the human embryonic stem cell line HS181, evaluated in a double-color system. . 2004-08-00. Pubmed ID: 15345126; DOI: 10.1089/scd.2004.13.337 KIe001-A 2004-08-00 2004-08-00 PubMed: 15345126 DOI: 10.1089/scd.2004.13.337Associated cell lines:
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Inzunza J, Sahlén S, Holmberg K, Strömberg AM, Teerijoki H, Blennow E, Hovatta O, Malmgren H
Comparative genomic hybridization and karyotyping of human embryonic stem cells reveals the occurrence of an isodicentric X chromosome after long-term cultivation
Inzunza J et al. Comparative genomic hybridization and karyotyping of human embryonic stem cells reveals the occurrence of an isodicentric X chromosome after long-term cultivation. . 2004-06-00. Pubmed ID: 15044603; DOI: 10.1093/molehr/gah051 KIe001-AKIe003-AKIe004-A 2004-06-00 2004-06-00 PubMed: 15044603 DOI: 10.1093/molehr/gah051 -
Baharvand H, Ashtiani SK, Valojerdi MR, Shahverdi A, Taee A, Sabour D
Establishment and in vitro differentiation of a new embryonic stem cell line from human blastocyst
Baharvand H et al. Establishment and in vitro differentiation of a new embryonic stem cell line from human blastocyst. . 2004-06-00. Pubmed ID: 15270778; DOI: 10.1111/j.1432-0436.2004.07205005.x RIe001-A 2004-06-00 2004-06-00 PubMed: 15270778 DOI: 10.1111/j.1432-0436.2004.07205005.xAssociated cell lines:
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Cowan CA, Klimanskaya I, McMahon J, Atienza J, Witmyer J, Zucker JP, Wang S, Morton CC, McMahon AP, Powers D, Melton DA
Derivation of embryonic stem-cell lines from human blastocysts
Cowan CA et al. Derivation of embryonic stem-cell lines from human blastocysts. . 2004-03-25. Pubmed ID: 14999088; DOI: 10.1056/nejmsr040330 HVRDe001-AHVRDe002-AHVRDe003-AHVRDe004-AHVRDe005-AHVRDe006-AHVRDe007-AHVRDe008-AHVRDe009-AHVRDe010-AHVRDe011-AHVRDe012-AHVRDe013-AHVRDe014-AHVRDe015-AHVRDe016-AHVRDe017-A 2004-03-25 2004-03-25 PubMed: 14999088 DOI: 10.1056/nejmsr040330 -
Abeyta MJ, Clark AT, Rodriguez RT, Bodnar MS, Pera RA, Firpo MT
Unique gene expression signatures of independently-derived human embryonic stem cell lines
Abeyta MJ et al. Unique gene expression signatures of independently-derived human embryonic stem cell lines. . 2004-03-15. Pubmed ID: 14749348; DOI: 10.1093/hmg/ddh068 UCSFe002-A 2004-03-15 2004-03-15 PubMed: 14749348 DOI: 10.1093/hmg/ddh068Associated cell lines:
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Park SP, Lee YJ, Lee KS, Ah Shin H, Cho HY, Chung KS, Kim EY, Lim JH
Establishment of human embryonic stem cell lines from frozen-thawed blastocysts using STO cell feeder layers
Park SP et al. Establishment of human embryonic stem cell lines from frozen-thawed blastocysts using STO cell feeder layers. . 2004-03-00. Pubmed ID: 14998970; DOI: 10.1093/humrep/deh102 MIHe001-AMIHe002-AMIHe003-AMIHe004-AMIHe005-AMIHe006-AMIHe007-AMIHe008-AMIHe009-A 2004-03-00 2004-03-00 PubMed: 14998970 DOI: 10.1093/humrep/deh102 -
Carpenter MK, Rosler ES, Fisk GJ, Brandenberger R, Ares X, Miura T, Lucero M, Rao MS
Properties of four human embryonic stem cell lines maintained in a feeder-free culture system
Carpenter MK et al. Properties of four human embryonic stem cell lines maintained in a feeder-free culture system. . 2004-02-00. Pubmed ID: 14745950; DOI: 10.1002/dvdy.10431 WAe001-AWAe007-AWAe009-AWAe014-A 2004-02-00 2004-02-00 PubMed: 14745950 DOI: 10.1002/dvdy.10431 -
Park JH, Kim SJ, Oh EJ, Moon SY, Roh SI, Kim CG, Yoon HS
Establishment and maintenance of human embryonic stem cells on STO, a permanently growing cell line
Park JH et al. Establishment and maintenance of human embryonic stem cells on STO, a permanently growing cell line. . 2003-12-00. Pubmed ID: 12930726; DOI: 10.1095/biolreprod.103.017467 MIZMe001-AMIZMe002-AMIZMe003-A 2003-12-00 2003-12-00 PubMed: 12930726 DOI: 10.1095/biolreprod.103.017467Associated cell lines:
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Zeng X, Chen J, Liu Y, Luo Y, Schulz TC, Robins AJ, Rao MS, Freed WJ
BG01V: a variant human embryonic stem cell line which exhibits rapid growth after passaging and reliable dopaminergic differentiation
Zeng X et al. BG01V: a variant human embryonic stem cell line which exhibits rapid growth after passaging and reliable dopaminergic differentiation. . 2004-00-00. Pubmed ID: 15798361 VIACe001-A-2 2004-00-00 2004-00-00 PubMed: 15798361Associated cell lines:
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Zeng X, Miura T, Luo Y, Bhattacharya B, Condie B, Chen J, Ginis I, Lyons I, Mejido J, Puri RK, Rao MS, Freed WJ
Properties of pluripotent human embryonic stem cells BG01 and BG02
Zeng X et al. Properties of pluripotent human embryonic stem cells BG01 and BG02. . 2004-00-00. Pubmed ID: 15153607; DOI: 10.1634/stemcells.22-3-292 VIACe001-AVIACe002-A 2004-00-00 2004-00-00 PubMed: 15153607 DOI: 10.1634/stemcells.22-3-292Associated cell lines:
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Heins N, Englund MC, Sjöblom C, Dahl U, Tonning A, Bergh C, Lindahl A, Hanson C, Semb H
Derivation, characterization, and differentiation of human embryonic stem cells
Heins N et al. Derivation, characterization, and differentiation of human embryonic stem cells. . 2004-00-00. Pubmed ID: 15153613; DOI: 10.1634/stemcells.22-3-367 CEBe001-ACEBe002-ACEBe006-ACEBe012-ACEBe015-ACEBe034-ACEBe002-A-1 2004-00-00 2004-00-00 PubMed: 15153613 DOI: 10.1634/stemcells.22-3-367 -
Pickering SJ, Braude PR, Patel M, Burns CJ, Trussler J, Bolton V, Minger S
Preimplantation genetic diagnosis as a novel source of embryos for stem cell research
Pickering SJ et al. Preimplantation genetic diagnosis as a novel source of embryos for stem cell research. . 2003-10-00. Pubmed ID: 14653899; DOI: 10.1016/s1472-6483(10)61877-9 KCLe001-A 2003-10-00 2003-10-00 PubMed: 14653899 DOI: 10.1016/s1472-6483(10)61877-9Associated cell lines:
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Hovatta O, Mikkola M, Gertow K, Strömberg AM, Inzunza J, Hreinsson J, Rozell B, Blennow E, Andäng M, Ahrlund-Richter L
A culture system using human foreskin fibroblasts as feeder cells allows production of human embryonic stem cells
Hovatta O et al. A culture system using human foreskin fibroblasts as feeder cells allows production of human embryonic stem cells. . 2003-07-00. Pubmed ID: 12832363; DOI: 10.1093/humrep/deg290 KIe001-AKIe002-A 2003-07-00 2003-07-00 PubMed: 12832363 DOI: 10.1093/humrep/deg290 -
Mitalipova M, Calhoun J, Shin S, Wininger D, Schulz T, Noggle S, Venable A, Lyons I, Robins A, Stice S
Human embryonic stem cell lines derived from discarded embryos
Mitalipova M et al. Human embryonic stem cell lines derived from discarded embryos. . 2003-00-00. Pubmed ID: 12968106; DOI: 10.1634/stemcells.21-5-521 VIACe001-AVIACe002-AVIACe003-AVIACe004-A 2003-00-00 2003-00-00 PubMed: 12968106 DOI: 10.1634/stemcells.21-5-521Associated cell lines:
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He Z, Huang S, Li Y, Zhang Q
[Human embryonic stem cell lines preliminarily established in China]
He Z et al. [Human embryonic stem cell lines preliminarily established in China]. . 2002-10-10. Pubmed ID: 12509934 SYSUe004-ASYSUe005-ASYSUe006-A 2002-10-10 2002-10-10 PubMed: 12509934Associated cell lines:
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Lanzendorf SE, Boyd CA, Wright DL, Muasher S, Oehninger S, Hodgen GD
Use of human gametes obtained from anonymous donors for the production of human embryonic stem cell lines
Lanzendorf SE et al. Use of human gametes obtained from anonymous donors for the production of human embryonic stem cell lines. . 2001-07-00. Pubmed ID: 11438331; DOI: 10.1016/s0015-0282(01)01825-8 EVMSe001-AEVMSe002-AEVMSe003-A 2001-07-00 2001-07-00 PubMed: 11438331 DOI: 10.1016/s0015-0282(01)01825-8Associated cell lines:
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Amit M, Carpenter MK, Inokuma MS, Chiu CP, Harris CP, Waknitz MA, Itskovitz-Eldor J, Thomson JA
Clonally derived human embryonic stem cell lines maintain pluripotency and proliferative potential for prolonged periods of culture
Amit M et al. Clonally derived human embryonic stem cell lines maintain pluripotency and proliferative potential for prolonged periods of culture. . 2000-11-15. Pubmed ID: 11071754; DOI: 10.1006/dbio.2000.9912 WAe009-A-1WAe009-A-2 2000-11-15 2000-11-15 PubMed: 11071754 DOI: 10.1006/dbio.2000.9912Associated cell lines:
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Reubinoff BE, Pera MF, Fong CY, Trounson A, Bongso A
Embryonic stem cell lines from human blastocysts: somatic differentiation in vitro
Reubinoff BE et al. Embryonic stem cell lines from human blastocysts: somatic differentiation in vitro. . 2000-04-00. Pubmed ID: 10748519; DOI: 10.1038/74447 ESIBIe001-AESIBIe002-A 2000-04-00 2000-04-00 PubMed: 10748519 DOI: 10.1038/74447Associated cell lines:
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Thomson JA, Itskovitz-Eldor J, Shapiro SS, Waknitz MA, Swiergiel JJ, Marshall VS, Jones JM
Embryonic stem cell lines derived from human blastocysts
Thomson JA et al. Embryonic stem cell lines derived from human blastocysts. . 1998-11-06. Pubmed ID: 9804556; DOI: 10.1126/science.282.5391.1145 WAe001-AWAe007-AWAe009-AWAe013-AWAe014-A 1998-11-06 1998-11-06 PubMed: 9804556 DOI: 10.1126/science.282.5391.1145 -
Blackwood DH, He L, Morris SW, McLean A, Whitton C, Thomson M, Walker MT, Woodburn K, Sharp CM, Wright AF, Shibasaki Y, St Clair DM, Porteous DJ, Muir WJ
A locus for bipolar affective disorder on chromosome 4p
Blackwood DH et al. A locus for bipolar affective disorder on chromosome 4p. . 1996-04-00. Pubmed ID: 8630499; DOI: 10.1038/ng0496-427 EDi010-AEDi010-BEDi011-AEDi011-BEDi011-CEDi012-AEDi012-BEDi012-CEDi013-AEDi013-BEDi013-CEDi014-AEDi014-BEDi014-CEDi015-AEDi015-CEDi016-AEDi016-CEDi017-AEDi017-BEDi017-CEDi018-AEDi018-BEDi018-C 1996-04-00 1996-04-00 PubMed: 8630499 DOI: 10.1038/ng0496-427 -
Goldman D, Goldin LR, Rathnagiri P, O'Brien SJ, Egeland JA, Merril CR
Twenty-seven protein polymorphisms by two-dimensional electrophoresis of serum, erythrocytes, and fibroblasts in two pedigrees
Goldman D et al. Twenty-seven protein polymorphisms by two-dimensional electrophoresis of serum, erythrocytes, and fibroblasts in two pedigrees. . 1985-09-00. Pubmed ID: 3863481; PMC: PMC1684690 KAUSTi004-AKAUSTi004-BKAUSTi005-AKAUSTi005-BKAUSTi005-C 1985-09-00 1985-09-00 PubMed: 3863481Associated cell lines:
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Aronson MM, Nichols WW, Mulivor RA, Greene AE, Coriell LL
Chromosome maps of cell lines with specific monosomic or trisomic portions of the genome in the NIGMS Human Genetic Mutant Cell Repository
Aronson MM et al. Chromosome maps of cell lines with specific monosomic or trisomic portions of the genome in the NIGMS Human Genetic Mutant Cell Repository. . 1983-00-00. Pubmed ID: 6661932; DOI: 10.1159/000131990 KAUSTi001-AKAUSTi003-AKAUSTi005-AKAUSTi005-BKAUSTi005-CKAUSTi001-B 1983-00-00 1983-00-00 PubMed: 6661932 DOI: 10.1159/000131990Associated cell lines:
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The human genetic mutant cell repository : list of genetic variants, chromosomal aberrations and normal cell cultures submitted to the repository / Institute for Medical Research, Camden, New Jersey.
(unknown author). The human genetic mutant cell repository : list of genetic variants, chromosomal aberrations and normal cell cultures submitted to the repository / Institute for Medical Research, Camden, New Jersey. . 1977-00-00. DOI: 10.5962/bhl.title.4090 KAUSTi003-AKAUSTi004-AKAUSTi004-BKAUSTi005-AKAUSTi005-BKAUSTi005-C 1977-00-00 1977-00-00 DOI: 10.5962/bhl.title.4090Associated cell lines:
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Errata
(unknown author). Errata. . 1975-00-00. DOI: 10.1159/000130510 KAUSTi001-AKAUSTi001-B 1975-00-00 1975-00-00 DOI: 10.1159/000130510Associated cell lines:
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de la Chapelle A, Miller RC, Greene AE, Coriell LL
A (4;11) translocation, balanced, XXXXp-Y, 49 chromosomes. Repository identification No. GM-157
de la Chapelle A et al. A (4;11) translocation, balanced, XXXXp-Y, 49 chromosomes. Repository identification No. GM-157. . 1975-00-00. Pubmed ID: 1132249; DOI: 10.1159/000130320 KAUSTi001-AKAUSTi001-B 1975-00-00 1975-00-00 PubMed: 1132249 DOI: 10.1159/000130320Associated cell lines:
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Mulivor R.A., Suchy S.F.
1992/1993 catalog of cell lines. NIGMS human genetic mutant cell repository. 16th edition.
Mulivor R.A. et al. 1992/1993 catalog of cell lines. NIGMS human genetic mutant cell repository. 16th edition. . . KAUSTi008-AKAUSTi008-BKAUSTi008-CKAUSTi008-DKAUSTi008-EKAUSTi008-FKAUSTi008-GAssociated cell lines:
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Electrophysiological Evaluation of Human Induced Pluripotent Stem Cell- Derived Cardiomyocytes Obtained by Different Methods
(unknown author). Electrophysiological Evaluation of Human Induced Pluripotent Stem Cell- Derived Cardiomyocytes Obtained by Different Methods. . . TAUi002-AAssociated cell lines:
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Janny Pineiro-Llanes, Lais da Silva, John Huang, Rodrigo Cristofoletti
Comparative Study of Basement-membrane Matrices for Human Stem Cell Maintenance and Intestinal Organoid Generation
Janny Pineiro-Llanes et al. Comparative Study of Basement-membrane Matrices for Human Stem Cell Maintenance and Intestinal Organoid Generation. . . SCTi003-AAssociated cell lines:
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