Publications associated with registered cell lines
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Graffmann Nina, Martins Soraia, Ljubikj Tijana, Matte Julie Carole, Bohndorf Martina, Wruck Wasco, Adjaye James
Generation of a Crigler-Najjar Syndrome Type I patient-derived induced pluripotent stem cell line CNS705 (HHUUKDi005-A)
Graffmann Nina et al. Generation of a Crigler-Najjar Syndrome Type I patient-derived induced pluripotent stem cell line CNS705 (HHUUKDi005-A). . 2021-03-00. DOI: 10.1016/j.scr.2021.102167 HHUUKDi005-A 2021-03-00 2021-03-00 DOI: 10.1016/j.scr.2021.102167Associated cell lines:
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Chen Zhi-ting, Zhao Zhen-hua, Chen Li-na, Fan Fei, Cai Guo-en, Weng Hui-dan, Wang Ying-qing, Liao Lian-ming, Chen Xiao-chun, Huang En, Ye Qin-yong
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 Zhi-ting 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. DOI: 10.1016/j.scr.2021.102175 FJMUUHi001-A 2021-03-00 2021-03-00 DOI: 10.1016/j.scr.2021.102175Associated 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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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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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). . 2021-01-15. Pubmed ID: 33482465; DOI: 10.1016/j.scr.2021.102178 BGUi011-ABGUi012-A 2021-01-15 2021-01-15 PubMed: 33482465 DOI: 10.1016/j.scr.2021.102178 -
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. . 2021-01-12. Pubmed ID: 33472125; DOI: 10.1016/j.scr.2021.102172 SIAISi006-ASIAISi007-ASIAISi008-A 2021-01-12 2021-01-12 PubMed: 33472125 DOI: 10.1016/j.scr.2021.102172Associated 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. . 2021-01-12. Pubmed ID: 33472124; DOI: 10.1016/j.scr.2021.102170 WMUi014-A 2021-01-12 2021-01-12 PubMed: 33472124 DOI: 10.1016/j.scr.2021.102170Associated 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 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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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. . 2021-01-12. Pubmed ID: 33465532; DOI: 10.1016/j.scr.2021.102173 SIAISi011-A 2021-01-12 2021-01-12 PubMed: 33465532 DOI: 10.1016/j.scr.2021.102173Associated 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. . 2021-01-11. Pubmed ID: 33428073; DOI: 10.1007/s10815-021-02063-x HUSTi002-A 2021-01-11 2021-01-11 PubMed: 33428073 DOI: 10.1007/s10815-021-02063-xAssociated 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. . 2021-01-09. Pubmed ID: 33454628; DOI: 10.1016/j.scr.2021.102157 JTUi002-ACSUXHi003-A 2021-01-09 2021-01-09 PubMed: 33454628 DOI: 10.1016/j.scr.2021.102157Associated 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. . 2021-01-09. Pubmed ID: 33477036; DOI: 10.1016/j.scr.2021.102166 GZHMCi003-A 2021-01-09 2021-01-09 PubMed: 33477036 DOI: 10.1016/j.scr.2021.102166Associated 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. . 2021-01-08. Pubmed ID: 33461039; DOI: 10.1016/j.scr.2021.102161 WAe001-AWAe001-A-21 2021-01-08 2021-01-08 PubMed: 33461039 DOI: 10.1016/j.scr.2021.102161Associated 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. . 2021-01-08. Pubmed ID: 33453578; DOI: 10.1016/j.scr.2021.102158 ZZUNEUi020-A 2021-01-08 2021-01-08 PubMed: 33453578 DOI: 10.1016/j.scr.2021.102158Associated 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. . 2021-01-08. Pubmed ID: 33450697; DOI: 10.1016/j.scr.2021.102163 ZZUSAHi003-A 2021-01-08 2021-01-08 PubMed: 33450697 DOI: 10.1016/j.scr.2021.102163Associated 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). . 2021-01-08. Pubmed ID: 33477035; DOI: 10.1016/j.scr.2021.102159 WMUi017-A 2021-01-08 2021-01-08 PubMed: 33477035 DOI: 10.1016/j.scr.2021.102159Associated cell lines:
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Zehravi Mehwish, WAHID MOHSIN, Ashraf Junaid
Episomal reprogramming of Duchenne muscular dystrophy patients derived CD3+ T cells towards induced pluripotent stem cells
Zehravi Mehwish et al. Episomal reprogramming of Duchenne muscular dystrophy patients derived CD3+ T cells towards induced pluripotent stem cells. . 2021-01-08. DOI: 10.12669/pjms.37.2.3388 MUSIi011-AMUSIi011-B 2021-01-08 2021-01-08 DOI: 10.12669/pjms.37.2.3388Associated 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. . 2021-01-08. Pubmed ID: 33465529; DOI: 10.1016/j.scr.2021.102160 SDQLCHi018-A 2021-01-08 2021-01-08 PubMed: 33465529 DOI: 10.1016/j.scr.2021.102160Associated 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. . 2021-01-08. Pubmed ID: 33453577; DOI: 10.1016/j.scr.2021.102165 SDQLCHi039-A 2021-01-08 2021-01-08 PubMed: 33453577 DOI: 10.1016/j.scr.2021.102165Associated 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. . 2021-01-08. Pubmed ID: 33465531; DOI: 10.1016/j.scr.2021.102162 SDQLCHi037-A 2021-01-08 2021-01-08 PubMed: 33465531 DOI: 10.1016/j.scr.2021.102162Associated 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. . 2021-01-05. Pubmed ID: 33429167; DOI: 10.1016/j.scr.2020.102154 LEIi015-ALEIi015-B 2021-01-05 2021-01-05 PubMed: 33429167 DOI: 10.1016/j.scr.2020.102154 -
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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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. . 2021-01-04. Pubmed ID: 33398492; DOI: 10.1007/s10561-020-09896-3 ZZUi010-A 2021-01-04 2021-01-04 PubMed: 33398492 DOI: 10.1007/s10561-020-09896-3Associated 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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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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Hou Cuilan, Xie Lijian, Qiu Qingzhu, Lin Hao, liu Wei, Sun Xiaomin, Zhang Yongwei, Xu Meng, Li Yun, Xiao Tingting
Generation of an induced pluripotent stem cell line from a Chinese Han infant with floating-harbor syndrome accompanied with dilated cardiomyopathy
Hou Cuilan et al. Generation of an induced pluripotent stem cell line from a Chinese Han infant with floating-harbor syndrome accompanied with dilated cardiomyopathy. . 2021-01-00. DOI: 10.1016/j.scr.2021.102182 SHETi001-A 2021-01-00 2021-01-00 DOI: 10.1016/j.scr.2021.102182Associated cell lines:
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Hou Cuilan, Liu Wei, Xie Lijian, Zheng Junmin, Chen Xiaonan, Sun Xiaomin, Zhang Yongwei, Xu Meng, Li Yun, Xiao Tingting
Generation of an induced pluripotent stem cell line from a Chinese Han child with arrhythmia
Hou Cuilan et al. Generation of an induced pluripotent stem cell line from a Chinese Han child with arrhythmia. . 2021-01-00. DOI: 10.1016/j.scr.2021.102183 SHETi002-A 2021-01-00 2021-01-00 DOI: 10.1016/j.scr.2021.102183Associated 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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Guo Jinghui, Fang Fang, Dai Qiuting, Zhang Wenxin, Di Weihai, Hu Jiaan, Zhao Jian, Cao Jiumei, Wang Ying
Generation of a human-derived induced pluripotent stem cell line (SIAISi012-A) from an 82-year-old healthy Chinese Han male
Guo Jinghui et al. Generation of a human-derived induced pluripotent stem cell line (SIAISi012-A) from an 82-year-old healthy Chinese Han male. . 2021-01-00. DOI: 10.1016/j.scr.2021.102186 SIAISi012-A 2021-01-00 2021-01-00 DOI: 10.1016/j.scr.2021.102186Associated cell lines:
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Han Hyeong-jun, Kim Jung-Hyun
Establishment of a TLR3 homozygous knockout human induced pluripotent stem cell line using CRISPR/Cas9
Han Hyeong-jun et al. Establishment of a TLR3 homozygous knockout human induced pluripotent stem cell line using CRISPR/Cas9. . 2021-01-00. DOI: 10.1016/j.scr.2021.102187 KSCBi005-A-6 2021-01-00 2021-01-00 DOI: 10.1016/j.scr.2021.102187Associated cell lines:
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Liu Xiaolin, Liu Yong, Ma Yanyan, Gong Yaoqin, Liu Qiji, Sun Wenjie, Guo Hui
Establishment of patient-specific induced pluripotent stem cell line SDUBMSi009-A from a patient with X-linked Lowe syndrome
Liu Xiaolin et al. Establishment of patient-specific induced pluripotent stem cell line SDUBMSi009-A from a patient with X-linked Lowe syndrome. . 2021-01-00. DOI: 10.1016/j.scr.2021.102171 SDUBMSi009-A 2021-01-00 2021-01-00 DOI: 10.1016/j.scr.2021.102171Associated cell lines:
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Kamand Morad, Louise Forsberg Sheena, Thomassen Mads, Ilieva Mirolyuba, Meyer Morten, Fex Svenningsen Åsa, Maria Michel Tanja
Establishment of an induced pluripotent stem (iPS) cell line (SDUKIi006-A) from a 21-year old male patient diagnosed with atypical autism disorder
Kamand Morad 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. . 2021-01-00. DOI: 10.1016/j.scr.2021.102185 SDUKIi006-A 2021-01-00 2021-01-00 DOI: 10.1016/j.scr.2021.102185Associated cell lines:
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Harding Philippa, Lima Cunha Dulce, Méjécase Cécile, Eintracht Jonathan, Toualbi Lyes, Sarkar Hajrah, Moosajee Mariya
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 Philippa 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. . 2021-01-00. DOI: 10.1016/j.scr.2021.102184 UCLi013-A 2021-01-00 2021-01-00 DOI: 10.1016/j.scr.2021.102184Associated cell lines:
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Hornig NC, Holterhus PM
Molecular basis of androgen insensitivity syndromes
Hornig NC et al. Molecular basis of androgen insensitivity syndromes. . 2020-12-29. Pubmed ID: 33385475; DOI: 10.1016/j.mce.2020.111146 SKLRMi001-A 2020-12-29 2020-12-29 PubMed: 33385475 DOI: 10.1016/j.mce.2020.111146Associated cell lines:
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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. . 2020-12-29. Pubmed ID: 33300436; DOI: 10.1080/15592294.2020.1861172 KSCBi007-A 2020-12-29 2020-12-29 PubMed: 33300436 DOI: 10.1080/15592294.2020.1861172Associated 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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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 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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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 BNIi001-ABNIi001-B 2020-12-24 2020-12-24 PubMed: 33388707 DOI: 10.1016/j.scr.2020.102141 -
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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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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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. . 2020-12-23. Pubmed ID: 33369228; DOI: 10.1002/2211-5463.13072 WAe001-AWAe001-A-15 2020-12-23 2020-12-23 PubMed: 33369228 DOI: 10.1002/2211-5463.13072Associated 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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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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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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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. . 2020-12-19. Pubmed ID: 33347831; DOI: 10.1016/j.expneurol.2020.113573 ZZUi004-ALUMCi002-ALUMCi003-AMUSIi004-AHIHCNi002-AICGi007-AIBCHi001-ACSSi008-ACSUXHi002-A 2020-12-19 2020-12-19 PubMed: 33347831 DOI: 10.1016/j.expneurol.2020.113573Associated cell lines:
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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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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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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-A 2020-12-16 2020-12-16 PubMed: 33268331 DOI: 10.1242/bio.055087Associated cell lines:
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Völkner C, Liedtke M, Petters J, Lukas J, Escobar HM, Knuebel G, Bullerdiek J, Holzmann C, Hermann A, Frech MJ
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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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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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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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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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-G 2020-12-10 2020-12-10 PubMed: 33333453 DOI: 10.1016/j.scr.2020.102119 -
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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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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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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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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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 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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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 -
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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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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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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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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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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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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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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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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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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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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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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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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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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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-A 2020-12-00 2020-12-00 PubMed: 33059130 DOI: 10.1016/j.scr.2020.102020Associated 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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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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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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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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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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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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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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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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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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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 -
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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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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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-B 2020-12-00 2020-12-00 PubMed: 33039804 DOI: 10.1016/j.scr.2020.102021 -
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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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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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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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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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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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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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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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 -
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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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 ICGi024-A 2020-12-00 2020-12-00 PubMed: 33212351 DOI: 10.1016/j.scr.2020.102076Associated 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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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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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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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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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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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-B 2020-12-00 2020-12-00 PubMed: 33264725 DOI: 10.1016/j.scr.2020.102089Associated 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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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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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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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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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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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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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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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 -
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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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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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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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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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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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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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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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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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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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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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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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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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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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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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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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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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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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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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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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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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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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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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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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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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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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 NDi001-A 2020-12-00 2020-12-00 PubMed: 33370871 DOI: 10.1016/j.scr.2020.102096Associated 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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Abdelalim EM
Modeling different types of diabetes using human pluripotent stem cells
Abdelalim EM. Modeling different types of diabetes using human pluripotent stem cells. . 2020-11-26. Pubmed ID: 33242105; DOI: 10.1007/s00018-020-03710-9 QBRIi007-A 2020-11-26 2020-11-26 PubMed: 33242105 DOI: 10.1007/s00018-020-03710-9Associated 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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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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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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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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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. . 2020-11-18. Pubmed ID: 33206286; DOI: 10.1007/s10571-020-01007-w NIMHi001-A 2020-11-18 2020-11-18 PubMed: 33206286 DOI: 10.1007/s10571-020-01007-wAssociated 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-AIPTi005-AIPTi007-A 2020-11-15 2020-11-15 PubMed: 32988331 DOI: 10.1089/scd.2020.0103 -
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. . 2020-11-12. Pubmed ID: 33179450; DOI: 10.1002/sctm.20-0322 ISMMSi002-BMHHi012-AMHHi013-AMHHi014-A 2020-11-12 2020-11-12 PubMed: 33179450 DOI: 10.1002/sctm.20-0322Associated 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. . 2020-11-12. Pubmed ID: 33223277; DOI: 10.1016/j.cmpb.2020.105831 ZJUi005-A 2020-11-12 2020-11-12 PubMed: 33223277 DOI: 10.1016/j.cmpb.2020.105831Associated 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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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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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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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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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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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. . 2020-11-03. Pubmed ID: 33142012; DOI: 10.1002/mds.28365 LCSBi001-A 2020-11-03 2020-11-03 PubMed: 33142012 DOI: 10.1002/mds.28365Associated 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 -
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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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 -
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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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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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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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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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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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. . 2020-10-26. Pubmed ID: 33106889; DOI: 10.1007/s00415-020-10218-6 CSSi008-A 2020-10-26 2020-10-26 PubMed: 33106889 DOI: 10.1007/s00415-020-10218-6Associated 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. . 2020-10-26. Pubmed ID: 33106888; DOI: 10.1007/s00415-020-10274-y HIHCNi002-A 2020-10-26 2020-10-26 PubMed: 33106888 DOI: 10.1007/s00415-020-10274-yAssociated 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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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. . 2020-10-23. 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 2020-10-23 2020-10-23 PubMed: 33098306 DOI: 10.1007/s12015-020-10061-2 -
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, 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-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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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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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. . 2020-10-07. Pubmed ID: 33025588; DOI: 10.1111/jnc.15207 BIONi010-C 2020-10-07 2020-10-07 PubMed: 33025588 DOI: 10.1111/jnc.15207Associated cell lines:
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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. . 2020-10-03. Pubmed ID: 33011821; DOI: 10.1007/s00018-020-03653-1 FAMRCi007-AFAMRCi007-B 2020-10-03 2020-10-03 PubMed: 33011821 DOI: 10.1007/s00018-020-03653-1Associated 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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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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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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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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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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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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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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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 -
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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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 -
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 -
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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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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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 -
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 -
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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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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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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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 -
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 -
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 -
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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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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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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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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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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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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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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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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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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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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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 -
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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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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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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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
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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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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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 -
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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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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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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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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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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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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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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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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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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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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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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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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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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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-36 2020-10-00 2020-10-00 PubMed: 32777767 DOI: 10.1016/j.scr.2020.101930Associated 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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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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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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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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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 SOD1L39R Linked Amyotrophic Lateral Sclerosis
Rajpurohit CS et al. Mechanistic Insights of Astrocyte-Mediated Hyperactive Autophagy and Loss of Motor Neuron Function in SOD1L39R 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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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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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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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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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 -
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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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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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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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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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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Zhang B
CRISPR/Cas gene therapy
Zhang B. CRISPR/Cas gene therapy. . 2020-09-22. Pubmed ID: 32959897; DOI: 10.1002/jcp.30064 ZSSYe001-A 2020-09-22 2020-09-22 PubMed: 32959897 DOI: 10.1002/jcp.30064Associated 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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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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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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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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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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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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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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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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56th EASD Annual Meeting of the European Association for the Study of Diabetes : 21-25 September 2020
(unknown author). 56th 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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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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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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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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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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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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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 PIP3 to support axon regeneration in the adult CNS
Nieuwenhuis B et al. PI 3-kinase delta enhances axonal PIP3 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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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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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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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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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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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. . 2020-07-25. Pubmed ID: 32721458; DOI: 10.1016/j.preteyeres.2020.100880 CABi003-A 2020-07-25 2020-07-25 PubMed: 32721458 DOI: 10.1016/j.preteyeres.2020.100880Associated cell lines:
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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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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 -
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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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-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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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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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 NIHTVBi014-A 2020-07-20 2020-07-20 PubMed: 32721894 DOI: 10.1016/j.scr.2020.101921Associated 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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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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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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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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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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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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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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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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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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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 NIDCRi001-A 2020-07-00 2020-07-00 PubMed: 32505898 DOI: 10.1016/j.scr.2020.101823Associated cell lines:
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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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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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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 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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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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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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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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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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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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Moya N, Shahryari A, Burtscher I, Beckenbauer J, Bakhti M, Lickert H
Generation of a homozygous ARX nuclear CFP (ARXnCFP/nCFP) reporter human iPSC line (HMGUi001-A-4)
Moya N et al. Generation of a homozygous ARX nuclear CFP (ARXnCFP/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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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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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 -
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 -
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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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 -
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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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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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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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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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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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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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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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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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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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 -
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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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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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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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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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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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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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 -
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-6UKERe006-BUKERe006-CUKERe006-D 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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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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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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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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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-B 2020-06-19 2020-06-19 PubMed: 32592954 DOI: 10.1016/j.scr.2020.101881Associated cell lines:
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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-F 2020-06-12 2020-06-12 PubMed: 32373648 DOI: 10.1016/j.omtm.2020.04.005Associated 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 -
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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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. . 2020-06-04. Pubmed ID: 32500482; DOI: 10.1007/s12015-020-09989-2; PMC: PMC7272136 CSSi001-A 2020-06-04 2020-06-04 PubMed: 32500482 DOI: 10.1007/s12015-020-09989-2Associated 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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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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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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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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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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Heck AM, Russo J, Wilusz J, Nishimura EO, Wilusz CJ
YTHDF2 destabilizes m6A-modified neural-specific RNAs to restrain differentiation in induced pluripotent stem cells
Heck AM et al. YTHDF2 destabilizes m6A-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-2 2020-05-06 2020-05-06 PubMed: 32384610 DOI: 10.3390/genes11050511Associated 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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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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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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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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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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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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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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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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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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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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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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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-A 2020-05-00 2020-05-00 PubMed: 32335389 DOI: 10.1016/j.scr.2020.101785Associated 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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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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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 CSUXHi002-A 2020-05-00 2020-05-00 PubMed: 32335388 DOI: 10.1016/j.scr.2020.101816Associated 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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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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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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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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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 INSAi002-A 2020-05-00 2020-05-00 PubMed: 32388441 DOI: 10.1016/j.scr.2020.101794Associated 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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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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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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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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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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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 -
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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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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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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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 -
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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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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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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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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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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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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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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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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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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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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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 -
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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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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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 -
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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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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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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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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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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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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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 SDQLCHi004-A 2020-04-01 2020-04-01 PubMed: 31794866 DOI: 10.1016/j.bbadis.2019.165624Associated 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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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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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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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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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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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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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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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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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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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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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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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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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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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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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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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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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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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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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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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
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