Publications associated with registered cell lines
Sort by:
-
Sun Lingyu, Zhu Xiyu, Zhang Xiaoxuan, Chen Guopu, Bian Feika, Wang Junxia, Zhou Qing, Wang Dongjin, Zhao Yuanjin
Induced cardiomyocytes-integrated conductive microneedle patch for treating myocardial infarction
Sun Lingyu et al. Induced cardiomyocytes-integrated conductive microneedle patch for treating myocardial infarction. . 2021-06-00. DOI: 10.1016/j.cej.2021.128723 NJDTHi001-A 2021-06-00 2021-06-00 DOI: 10.1016/j.cej.2021.128723Associated cell lines:
-
Woo MS, Ufer F, Rothammer N, Di Liberto G, Binkle L, Haferkamp U, Sonner JK, Engler JB, Hornig S, Bauer S, Wagner I, Egervari K, Raber J, Duvoisin RM, Pless O, Merkler D, Friese MA
Neuronal metabotropic glutamate receptor 8 protects against neurodegeneration in CNS inflammation
Woo MS et al. Neuronal metabotropic glutamate receptor 8 protects against neurodegeneration in CNS inflammation. . 2021-05-03. Pubmed ID: 33661276; DOI: 10.1084/jem.20201290; PMC: PMC7938362 ZIPi013-B 2021-05-03 2021-05-03 PubMed: 33661276 DOI: 10.1084/jem.20201290Associated cell lines:
-
Yin Xiaojuan, Zhao Danhua, Tian Zhichen, Chen Jia, Chi Jinghan, Ke Yan, He Liu, Zhang Xuan, He Yanmei, Feng Zhichun
Generation of an induced pluripotent stem cell line from a patient with surfactant metabolism dysfunction carrying ABCA3 mutations
Yin Xiaojuan et al. Generation of an induced pluripotent stem cell line from a patient with surfactant metabolism dysfunction carrying ABCA3 mutations. . 2021-05-00. DOI: 10.1016/j.scr.2021.102286 SMCPGHi001-A 2021-05-00 2021-05-00 DOI: 10.1016/j.scr.2021.102286Associated cell lines:
-
Huang Y, Wu H, Han X, Wu J, Yu M, Zhao ZA, Shen Z, Hu S, Lei W
Generation of an EFNB2-2A-mCherry reporter human embryonic stem cell line using CRISPR/Cas9-mediated site-specific homologous recombination
Huang Y et al. Generation of an EFNB2-2A-mCherry reporter human embryonic stem cell line using CRISPR/Cas9-mediated site-specific homologous recombination. . 2021-04-00. Pubmed ID: 33611045; DOI: 10.1016/j.scr.2021.102241 WAe001-AWAe001-A-57 2021-04-00 2021-04-00 PubMed: 33611045 DOI: 10.1016/j.scr.2021.102241Associated cell lines:
-
Hong W, Yun W, Choi W, Son D, Song G, You S
Generation of a WA14 hESC sub-line carrying a hemizygous ABCD1 (C.1696_1710 del) mutation introduced by CRISPR/Cas9 technology
Hong W et al. Generation of a WA14 hESC sub-line carrying a hemizygous ABCD1 (C.1696_1710 del) mutation introduced by CRISPR/Cas9 technology. . 2021-04-00. Pubmed ID: 33611043; DOI: 10.1016/j.scr.2021.102244 WAe014-A-1 2021-04-00 2021-04-00 PubMed: 33611043 DOI: 10.1016/j.scr.2021.102244Associated cell lines:
-
Guan J, Tian G, Dong R, Zhang H, Yang X, Li Y, Gai Z, Liu Y
Induced pluripotent stem cell line (SDQLCHi041-A) from a male patient with mucopolysaccharidosis type IIIB
Guan J et al. Induced pluripotent stem cell line (SDQLCHi041-A) from a male patient with mucopolysaccharidosis type IIIB. . 2021-04-00. Pubmed ID: 33550137; DOI: 10.1016/j.scr.2021.102212 SDQLCHi021-ASDQLCHi041-A 2021-04-00 2021-04-00 PubMed: 33550137 DOI: 10.1016/j.scr.2021.102212Associated cell lines:
-
Yi C, Dingya C, Nengqing L, Hongmei G, Yi L, Huimin Z, Jiajia X, Bing S, Xiaofang S
Generation of induced pluripotent stem cell GZHMCi005-A from amniotic fluid-derived cells with duplication of chromosome 8p
Yi C et al. Generation of induced pluripotent stem cell GZHMCi005-A from amniotic fluid-derived cells with duplication of chromosome 8p. . 2021-04-00. Pubmed ID: 33588214; DOI: 10.1016/j.scr.2021.102226 GZHMCi005-A 2021-04-00 2021-04-00 PubMed: 33588214 DOI: 10.1016/j.scr.2021.102226Associated cell lines:
-
Ma Y, Wang Z, Liu X, Sun W, Gong Y, Liu G, Sun G
Generation and characterization of an integration-free iPSC line SDUBMSi006-A from a patient with Alport syndrome caused by COL4A3 gene mutations
Ma Y et al. Generation and characterization of an integration-free iPSC line SDUBMSi006-A from a patient with Alport syndrome caused by COL4A3 gene mutations. . 2021-04-00. Pubmed ID: 33601099; DOI: 10.1016/j.scr.2021.102237 SDUBMSi006-A 2021-04-00 2021-04-00 PubMed: 33601099 DOI: 10.1016/j.scr.2021.102237Associated cell lines:
-
Kondrateva E, Demchenko A, Slesarenko Y, Pozhitnova V, Yasinovsky M, Amelina E, Tabakov V, Voronina E, Lavrov A, Smirnikhina S
Generation of two induced pluripotent stem cell lines (RCMGi004-A and -B) from human skin fibroblasts of a cystic fibrosis patient with compound heterozygous F508del/W1282X mutations in CFTR gene
Kondrateva E et al. Generation of two induced pluripotent stem cell lines (RCMGi004-A and -B) from human skin fibroblasts of a cystic fibrosis patient with compound heterozygous F508del/W1282X mutations in CFTR gene. . 2021-04-00. Pubmed ID: 33607467; DOI: 10.1016/j.scr.2021.102232 RCMGi004-ARCMGi004-B 2021-04-00 2021-04-00 PubMed: 33607467 DOI: 10.1016/j.scr.2021.102232Associated cell lines:
-
Guo J, Fang F, Dai Q, Zhang W, Di W, Hu J, Zhao J, Cao J, Wang Y
Generation of a human-derived induced pluripotent stem cell line (SIAISi012-A) from an 82-year-old healthy Chinese Han male
Guo J et al. Generation of a human-derived induced pluripotent stem cell line (SIAISi012-A) from an 82-year-old healthy Chinese Han male. . 2021-04-00. Pubmed ID: 33610016; DOI: 10.1016/j.scr.2021.102186 SIAISi012-A 2021-04-00 2021-04-00 PubMed: 33610016 DOI: 10.1016/j.scr.2021.102186Associated cell lines:
-
Silva TP, Pereira CA, Oliveira AR, Raposo AC, Arez M, Cabral JMS, Milagre I, Carmo-Fonseca M, da Rocha ST
Generation and characterization of induced pluripotent stem cells from a family carrying the BRCA1 mutation c.3612delA
Silva TP et al. Generation and characterization of induced pluripotent stem cells from a family carrying the BRCA1 mutation c.3612delA. . 2021-04-00. Pubmed ID: 33631522; DOI: 10.1016/j.scr.2021.102242 IBBISTi001-AIBBISTi001-BIBBISTi001-CIBBISTi001-DIBBISTi002-AIBBISTi002-B 2021-04-00 2021-04-00 PubMed: 33631522 DOI: 10.1016/j.scr.2021.102242Associated cell lines:
-
Gonsior K, Kaucher GA, Pelz P, Schumann D, Gansel M, Kuhs S, Klockgether T, Forlani S, Durr A, Hauser S, Rattay TW, Synofzik M, Hengel H, Schöls L, Rieß OH, Hübener-Schmid J
PolyQ-expanded ataxin-3 protein levels in peripheral blood mononuclear cells correlate with clinical parameters in SCA3: a pilot study
Gonsior K et al. PolyQ-expanded ataxin-3 protein levels in peripheral blood mononuclear cells correlate with clinical parameters in SCA3: a pilot study. . 2021-04-00. Pubmed ID: 33106888; DOI: 10.1007/s00415-020-10274-y HIHCNi002-A 2021-04-00 2021-04-00 PubMed: 33106888 DOI: 10.1007/s00415-020-10274-yAssociated cell lines:
-
Han HJ, Kim JH
Establishment of a TLR3 homozygous knockout human induced pluripotent stem cell line using CRISPR/Cas9
Han HJ et al. Establishment of a TLR3 homozygous knockout human induced pluripotent stem cell line using CRISPR/Cas9. . 2021-04-00. Pubmed ID: 33582546; DOI: 10.1016/j.scr.2021.102187 KSCBi005-AKSCBi005-A-5KSCBi005-A-6 2021-04-00 2021-04-00 PubMed: 33582546 DOI: 10.1016/j.scr.2021.102187Associated cell lines:
-
Li Y, Dong R, Wang G, Zhang H, Yang X, Li Z, Guan J, Gai Z, Liu Y
Establishment of a novel human iPSC line (SDQLCHi032-A) derived from a patient with primary hypertrophic osteoarthropathy caused by HPGD homozygous mutation
Li Y et al. Establishment of a novel human iPSC line (SDQLCHi032-A) derived from a patient with primary hypertrophic osteoarthropathy caused by HPGD homozygous mutation. . 2021-04-00. Pubmed ID: 33550138; DOI: 10.1016/j.scr.2021.102217 SDQLCHi032-A 2021-04-00 2021-04-00 PubMed: 33550138 DOI: 10.1016/j.scr.2021.102217Associated cell lines:
-
Zhang B
CRISPR/Cas gene therapy
Zhang B. CRISPR/Cas gene therapy. . 2021-04-00. Pubmed ID: 32959897; DOI: 10.1002/jcp.30064 ZSSYe001-A 2021-04-00 2021-04-00 PubMed: 32959897 DOI: 10.1002/jcp.30064Associated cell lines:
-
Yuan A, Tao R, Yu S, Jing N, Sun J
Generation of human induced pluripotent stem cell line FDCHDPi001-A from a Chinese Han Tourette's syndrome patient
Yuan A et al. Generation of human induced pluripotent stem cell line FDCHDPi001-A from a Chinese Han Tourette's syndrome patient. . 2021-04-00. Pubmed ID: 33607468; DOI: 10.1016/j.scr.2021.102227 FDCHDPi001-A 2021-04-00 2021-04-00 PubMed: 33607468 DOI: 10.1016/j.scr.2021.102227Associated cell lines:
-
Tian X, Fu W, Guo G, Huang S, Dong Y, Li X, Dong J, Zhao X, Zhang Y
Generation of a human iPSC line ZZUNEUi015-A from a patient with hypertrophic cardiomyopathy caused by mutation in ALPK3
Tian X et al. Generation of a human iPSC line ZZUNEUi015-A from a patient with hypertrophic cardiomyopathy caused by mutation in ALPK3. . 2021-04-00. Pubmed ID: 33607470; DOI: 10.1016/j.scr.2021.102247 ZZUNEUi015-A 2021-04-00 2021-04-00 PubMed: 33607470 DOI: 10.1016/j.scr.2021.102247Associated cell lines:
-
Tangprasittipap A, Chumchuen S, Pornratananont G, Kitiyanant N, Hongeng S
Generation of a human induced pluripotent stem cells (MUi015-A) from skin fibroblast of retinoblastoma patient with 13q deletion syndrome
Tangprasittipap A et al. Generation of a human induced pluripotent stem cells (MUi015-A) from skin fibroblast of retinoblastoma patient with 13q deletion syndrome. . 2021-04-00. Pubmed ID: 33550139; DOI: 10.1016/j.scr.2021.102211 MUi015-A 2021-04-00 2021-04-00 PubMed: 33550139 DOI: 10.1016/j.scr.2021.102211Associated cell lines:
-
Sun X, Zhou X, Dong B, Wang C, Xiao X, Wang Y
Generation of a gene-corrected isogenic iPSC line (AHQUi001-A-1) from a patient with familial hypertriglyceridemia (FHTG) carrying a heterozygous p.C310R (c.928 T > C) mutation in LPL gene using CRISPR/Cas9
Sun X et al. Generation of a gene-corrected isogenic iPSC line (AHQUi001-A-1) from a patient with familial hypertriglyceridemia (FHTG) carrying a heterozygous p.C310R (c.928 T > C) mutation in LPL gene using CRISPR/Cas9. . 2021-04-00. Pubmed ID: 33592566; DOI: 10.1016/j.scr.2021.102230 AHQUi001-AAHQUi001-A-1 2021-04-00 2021-04-00 PubMed: 33592566 DOI: 10.1016/j.scr.2021.102230Associated cell lines:
-
Huang S, Fu W, Guo G, Tiana X, Zhao X, Dong J, Li X, Yang H
Generation of a hiPSC line ZZUNEUi017-A from a patient with dilated cardiomyopathy caused by mutation in TTN
Huang S et al. Generation of a hiPSC line ZZUNEUi017-A from a patient with dilated cardiomyopathy caused by mutation in TTN. . 2021-04-00. Pubmed ID: 33610015; DOI: 10.1016/j.scr.2021.102248 ZZUSAHi002-AZZUNEUi017-A 2021-04-00 2021-04-00 PubMed: 33610015 DOI: 10.1016/j.scr.2021.102248Associated cell lines:
-
Hedges EC, Topp S, Shaw CE, Nishimura AL
Generation of six induced pluripotent stem cell lines from patients with amyotrophic lateral sclerosis with associated genetic mutations in either FUS or ANXA11
Hedges EC et al. Generation of six induced pluripotent stem cell lines from patients with amyotrophic lateral sclerosis with associated genetic mutations in either FUS or ANXA11. . 2021-04-00. Pubmed ID: 33610019; DOI: 10.1016/j.scr.2021.102246; PMC: PMC7988463 KCLi008-AKCLi009-AKCLi010-AKCLi011-AKCLi012-AKCLi013-A 2021-04-00 2021-04-00 PubMed: 33610019 DOI: 10.1016/j.scr.2021.102246 -
Zhang C, Wei Y, Zhang Y, Zhang J, Xing Q, Zhou M, Shan Y
Establishment of a CRISPR/Cas9-mediated ANP32A homozygous knockout human embryonic stem cell line
Zhang C et al. Establishment of a CRISPR/Cas9-mediated ANP32A homozygous knockout human embryonic stem cell line. . 2021-04-00. Pubmed ID: 33607472; DOI: 10.1016/j.scr.2021.102234 WAe001-A-53 2021-04-00 2021-04-00 PubMed: 33607472 DOI: 10.1016/j.scr.2021.102234Associated cell lines:
-
Sawangareetrakul P, Ngiwsara L, Champattanachai V, Chokchaichamnankit D, Saharat K, Ketudat Cairns JR, Srisomsap C, Khwanraj K, Dharmasaroja P, Pulkes T, Svasti J
Aberrant proteins expressed in skin fibroblasts of Parkinson's disease patients carrying heterozygous variants of glucocerebrosidase and parkin genes
Sawangareetrakul P et al. Aberrant proteins expressed in skin fibroblasts of Parkinson's disease patients carrying heterozygous variants of glucocerebrosidase and parkin genes. . 2021-04-00. Pubmed ID: 33732455; DOI: 10.3892/br.2021.1412; PMC: PMC7907964 RCPCMi004-A 2021-04-00 2021-04-00 PubMed: 33732455 DOI: 10.3892/br.2021.1412Associated cell lines:
-
Schmid B, Holst B, Poulsen U, Jørring I, Clausen C, Rasmussen M, Mau-Holzmann UA, Steeg R, Nuthall H, Ebneth A, Cabrera-Socorro A
Generation of two gene edited iPSC-lines carrying a DOX-inducible NGN2 expression cassette with and without GFP in the AAVS1 locus
Schmid B et al. Generation of two gene edited iPSC-lines carrying a DOX-inducible NGN2 expression cassette with and without GFP in the AAVS1 locus. . 2021-04-00. Pubmed ID: 33610017; DOI: 10.1016/j.scr.2021.102240 BIONi010-CBIONi010-C-13BIONi010-C-15 2021-04-00 2021-04-00 PubMed: 33610017 DOI: 10.1016/j.scr.2021.102240Associated cell lines:
-
Guan J, Yan B, Zhang H, Liu C, Li Y, Yang X, Li Z, Gai Z, Liu Y
Generation of a human induced pluripotent stem cell line (SDQLCHi036-A) from a patient with ornithine transcarbamylase deficiency carrying a deletion involving 3-9 exons of OTC gene
Guan J et al. Generation of a human induced pluripotent stem cell line (SDQLCHi036-A) from a patient with ornithine transcarbamylase deficiency carrying a deletion involving 3-9 exons of OTC gene. . 2021-04-00. Pubmed ID: 33550136; DOI: 10.1016/j.scr.2021.102220 SDQLCHi036-A 2021-04-00 2021-04-00 PubMed: 33550136 DOI: 10.1016/j.scr.2021.102220Associated cell lines:
-
Guo Y, Wang J, Wang Z, Lou Y, Chen W, Sheng M, Wang Y, Zhang B, Gao L, Feng J
Establishment of an induced pluripotent stem cell line (ZJSHi001-A) from a patient with epileptic encephalopathy carrying KCNB1 Glu330Asp mutation
Guo Y et al. Establishment of an induced pluripotent stem cell line (ZJSHi001-A) from a patient with epileptic encephalopathy carrying KCNB1 Glu330Asp mutation. . 2021-04-00. Pubmed ID: 33607466; DOI: 10.1016/j.scr.2021.102224 ZJSHi001-A 2021-04-00 2021-04-00 PubMed: 33607466 DOI: 10.1016/j.scr.2021.102224Associated cell lines:
-
Schmid B, Holst B, Clausen C, Bahnassawy L, Reinhardt P, Bakker MHM, Díaz-Guerra E, Vicario C, Martino-Adami PV, Thoenes M, Ramirez A, Fliessbach K, Grezella C, Brüstle O, Peitz M, Ebneth A, Cabrera-Socorro A
Generation of a set of isogenic iPSC lines carrying all APOE genetic variants (Ɛ2/Ɛ3/Ɛ4) and knock-out for the study of APOE biology in health and disease
Schmid B et al. Generation of a set of isogenic iPSC lines carrying all APOE genetic variants (Ɛ2/Ɛ3/Ɛ4) and knock-out for the study of APOE biology in health and disease. . 2021-04-00. Pubmed ID: 33556820; DOI: 10.1016/j.scr.2021.102180 UKBi011-AUKBi011-A-1UKBi011-A-2UKBi011-A-3UKBi011-A-4 2021-04-00 2021-04-00 PubMed: 33556820 DOI: 10.1016/j.scr.2021.102180Associated cell lines:
-
Merkert S, Wunderlich S, Beier J, Franke A, Schwanke K, Göhring G, Kraft T, Francino A, Zweigerdt R, Martin U
Generation of two iPSC clones (MHHi021-A and MHHi021-B) from a patient with hypertrophic cardiomyopathy with p.Arg723Gly mutation in the MYH7 gene
Merkert S et al. Generation of two iPSC clones (MHHi021-A and MHHi021-B) from a patient with hypertrophic cardiomyopathy with p.Arg723Gly mutation in the MYH7 gene. . 2021-04-00. Pubmed ID: 33578365; DOI: 10.1016/j.scr.2021.102208 MHHi021-AMHHi021-B 2021-04-00 2021-04-00 PubMed: 33578365 DOI: 10.1016/j.scr.2021.102208 -
Liszewska E, Majchrowicz L, Krogulec E, Kotulska K, Kaczmarek L, Kalita K, Dobrzyń A, Jaworski J
Establishment of two hiPSC lines (IIMCBi001-A and IIMCBi002-A) from dermal fibroblasts of healthy donors and characterization of their cell cycle
Liszewska E et al. Establishment of two hiPSC lines (IIMCBi001-A and IIMCBi002-A) from dermal fibroblasts of healthy donors and characterization of their cell cycle. . 2021-04-00. Pubmed ID: 33588215; DOI: 10.1016/j.scr.2021.102225 IIMCBi001-AIIMCBi002-A 2021-04-00 2021-04-00 PubMed: 33588215 DOI: 10.1016/j.scr.2021.102225Associated cell lines:
-
Lu HE, Pan YL, Ko HW, Hsu SH, Wen CH, Hsu YC
Generation of induced pluripotent stem cells FIRDIi001-A from a Taiwanese subject carrying ALDH2 pE487K mutation
Lu HE et al. Generation of induced pluripotent stem cells FIRDIi001-A from a Taiwanese subject carrying ALDH2 pE487K mutation. . 2021-04-00. Pubmed ID: 33592568; DOI: 10.1016/j.scr.2021.102229 MMCi001-AFIRDIi001-A 2021-04-00 2021-04-00 PubMed: 33592568 DOI: 10.1016/j.scr.2021.102229Associated cell lines:
-
Laverde-Paz MJ, Nuytemans K, Wang L, Vance JM, Pericak-Vance MA, Dykxhoorn DM, Cukier HN
Derivation of stem cell line UMi028-A-2 containing a CRISPR/Cas9 induced Alzheimer's disease risk variant p.S1038C in the TTC3 gene
Laverde-Paz MJ et al. Derivation of stem cell line UMi028-A-2 containing a CRISPR/Cas9 induced Alzheimer's disease risk variant p.S1038C in the TTC3 gene. . 2021-04-00. Pubmed ID: 33626494; DOI: 10.1016/j.scr.2021.102258 UMi028-AUMi028-A-2 2021-04-00 2021-04-00 PubMed: 33626494 DOI: 10.1016/j.scr.2021.102258Associated cell lines:
-
Ding Y, O'Brien A, de la Cruz BM, Yang M, Fitzgerald J, Yang G, Li W, McInerney V, Krawczyk J, Lynch SA, Howard L, Allen NM, O'Brien T, Gallagher L, Shen S
Derivation of iPSC lines from two patients with autism spectrum disorder carrying NRXN1α deletion (NUIGi041-A, NUIG041-B; NUIGi045-A) and one sibling control (NUIGi042-A, NUIGi042-B)
Ding Y et al. Derivation of iPSC lines from two patients with autism spectrum disorder carrying NRXN1α deletion (NUIGi041-A, NUIG041-B; NUIGi045-A) and one sibling control (NUIGi042-A, NUIGi042-B). . 2021-04-00. Pubmed ID: 33578364; DOI: 10.1016/j.scr.2021.102222 NUIGi041-ANUIGi042-ANUIGi045-ANUIGi041-BNUIGi042-B 2021-04-00 2021-04-00 PubMed: 33578364 DOI: 10.1016/j.scr.2021.102222Associated cell lines:
-
Ji W, Wang D, Chen C, Chen H, Ding Y, Li C, Rong X, Shan X, Chu M, Shen X, Guo X
Generation of an induced pluripotent stem cell line from a Bartter syndrome patient with the homozygote mutation p.A244D (c.731C>A) in SLC12A1 gene
Ji W et al. Generation of an induced pluripotent stem cell line from a Bartter syndrome patient with the homozygote mutation p.A244D (c.731C>A) in SLC12A1 gene. . 2021-04-00. Pubmed ID: 33607471; DOI: 10.1016/j.scr.2021.102228 WMUi019-A 2021-04-00 2021-04-00 PubMed: 33607471 DOI: 10.1016/j.scr.2021.102228Associated cell lines:
-
Haase A, Kohrn T, Fricke V, Ricci Signorini ME, Witte M, Göhring G, Gruh I, Martin U
Establishment of MHHi001-A-5, a GCaMP6f and RedStar dual reporter human iPSC line for in vitro and in vivo characterization and in situ tracing of iPSC derivatives
Haase A et al. Establishment of MHHi001-A-5, a GCaMP6f and RedStar dual reporter human iPSC line for in vitro and in vivo characterization and in situ tracing of iPSC derivatives. . 2021-04-00. Pubmed ID: 33571874; DOI: 10.1016/j.scr.2021.102206 MHHi001-AMHHi001-A-5 2021-04-00 2021-04-00 PubMed: 33571874 DOI: 10.1016/j.scr.2021.102206Associated cell lines:
-
Fan Y, Liu F, Fan LY, Mao CY, Liu H, Zhang C, Yuan YP, Yang J, Wang YL, Liu YT, Shi CH, Xu YM
Generation of an induced pluripotent stem cell line (ZZUi020-A) from a patient with Parkinson's disease harboring the intermediate-length GGC repeat expansions in the NOTCH2NLC gene
Fan Y et al. Generation of an induced pluripotent stem cell line (ZZUi020-A) from a patient with Parkinson's disease harboring the intermediate-length GGC repeat expansions in the NOTCH2NLC gene. . 2021-04-00. Pubmed ID: 33626493; DOI: 10.1016/j.scr.2021.102257 ZZUi020-A 2021-04-00 2021-04-00 PubMed: 33626493 DOI: 10.1016/j.scr.2021.102257Associated cell lines:
-
Sims CHC, Autio MI, Buskin A, Cheung C, Heer R, Foo RSY, Wang X
Modified CRISPR/Cas9 mediated generation of two MKK7 knockout human embryonic stem cell lines
Sims CHC et al. Modified CRISPR/Cas9 mediated generation of two MKK7 knockout human embryonic stem cell lines. . 2021-04-00. Pubmed ID: 33611044; DOI: 10.1016/j.scr.2021.102238 WAe001-AWAe001-A-54WAe001-A-55 2021-04-00 2021-04-00 PubMed: 33611044 DOI: 10.1016/j.scr.2021.102238Associated cell lines:
-
Fogerty J, Perkins BD
Knockout of the CEP290 gene in human induced pluripotent stem cells
Fogerty J et al. Knockout of the CEP290 gene in human induced pluripotent stem cells. . 2021-04-00. Pubmed ID: 33626495; DOI: 10.1016/j.scr.2021.102243 CEIi001-A 2021-04-00 2021-04-00 PubMed: 33626495 DOI: 10.1016/j.scr.2021.102243Associated cell lines:
-
Guo X, Wang D, Shan X, Yang L, Ding Y, Chen H, Rong X, Chu M, Lin J, Chen C
Establishment of an induced pluripotent stem cell line from a Antley-Bixler Syndrome (ABS) patient with the homozygote mutation p.R457H (c.1370G>A) in POR gene
Guo X et al. Establishment of an induced pluripotent stem cell line from a Antley-Bixler Syndrome (ABS) patient with the homozygote mutation p.R457H (c.1370G>A) in POR gene. . 2021-04-00. Pubmed ID: 33631521; DOI: 10.1016/j.scr.2021.102261 WMUi018-A 2021-04-00 2021-04-00 PubMed: 33631521 DOI: 10.1016/j.scr.2021.102261Associated cell lines:
-
Campostrini G, Meraviglia V, Giacomelli E, van Helden RWJ, Yiangou L, Davis RP, Bellin M, Orlova VV, Mummery CL
Generation, functional analysis and applications of isogenic three-dimensional self-aggregating cardiac microtissues from human pluripotent stem cells
Campostrini G et al. Generation, functional analysis and applications of isogenic three-dimensional self-aggregating cardiac microtissues from human pluripotent stem cells. . 2021-03-26. Pubmed ID: 33772245; DOI: 10.1038/s41596-021-00497-2 LUMCi027-A 2021-03-26 2021-03-26 PubMed: 33772245 DOI: 10.1038/s41596-021-00497-2Associated cell lines:
-
Dai Q, Di W, Zhang Y, Gu S, Zhao J, Zhang B, Wang Y
Generation of a human induced pluripotent stem cell line (SIAISi010-A) from a 31-year-old healthy donor with Chinese Han genetic background
Dai Q et al. Generation of a human induced pluripotent stem cell line (SIAISi010-A) from a 31-year-old healthy donor with Chinese Han genetic background. . 2021-03-26. Pubmed ID: 33799282; DOI: 10.1016/j.scr.2021.102314 SIAISi010-A 2021-03-26 2021-03-26 PubMed: 33799282 DOI: 10.1016/j.scr.2021.102314Associated cell lines:
-
Antonov SA, Novosadova EV
Current State-of-the-Art and Unresolved Problems in Using Human Induced Pluripotent Stem Cell-Derived Dopamine Neurons for Parkinson's Disease Drug Development
Antonov SA et al. Current State-of-the-Art and Unresolved Problems in Using Human Induced Pluripotent Stem Cell-Derived Dopamine Neurons for Parkinson's Disease Drug Development. . 2021-03-25. Pubmed ID: 33806103; DOI: 10.3390/ijms22073381 GIBHi003-ARCPCMi004-A 2021-03-25 2021-03-25 PubMed: 33806103 DOI: 10.3390/ijms22073381Associated cell lines:
-
Tang X, Fu J, Chen Z, Luo L, Li DW, Liu Y
Generation of a homozygous CRISPR/Cas9-mediated knockout H9 hESC subline for the MERTK locus
Tang X et al. Generation of a homozygous CRISPR/Cas9-mediated knockout H9 hESC subline for the MERTK locus. . 2021-03-24. Pubmed ID: 33812335; DOI: 10.1016/j.scr.2021.102310 WAe009-A-39 2021-03-24 2021-03-24 PubMed: 33812335 DOI: 10.1016/j.scr.2021.102310Associated cell lines:
-
Longobardi E, Miceli F, Secondo A, Cicatiello R, Izzo A, Tinto N, Moutton S, Tran Mau-Them F, Vitobello A, Taglialatela M
Generation of an iPSC line (UNINAi001-A) from a girl with neonatal-onset epilepsy and non-syndromic intellectual disability carrying the homozygous KCNQ3 p.PHE534ILEfs*15 variant and of an iPSC line (UNINAi002-A) from a non-carrier, unaffected brother
Longobardi E et al. Generation of an iPSC line (UNINAi001-A) from a girl with neonatal-onset epilepsy and non-syndromic intellectual disability carrying the homozygous KCNQ3 p.PHE534ILEfs*15 variant and of an iPSC line (UNINAi002-A) from a non-carrier, unaffected brother. . 2021-03-24. Pubmed ID: 33799276; DOI: 10.1016/j.scr.2021.102311 UNINAi001-AUNINAi002-A 2021-03-24 2021-03-24 PubMed: 33799276 DOI: 10.1016/j.scr.2021.102311Associated cell lines:
-
Xiao X, Chen Y, Peng L, Zhang T
Generation of a homozygous ALX1 knockout human embryonic stem cell line (WAe001-A-060) by a CRISPR/Cas9 system
Xiao X et al. Generation of a homozygous ALX1 knockout human embryonic stem cell line (WAe001-A-060) by a CRISPR/Cas9 system. . 2021-03-24. Pubmed ID: 33799274; DOI: 10.1016/j.scr.2021.102309 WAe001-AWAe001-A-60 2021-03-24 2021-03-24 PubMed: 33799274 DOI: 10.1016/j.scr.2021.102309Associated cell lines:
-
Du M, Li L, Hu Y, Mi H, Wang T
Derivation of a human induced pluripotent stem cell (hiPSC) line (PUMCSMi001-A) from peripheral blood mononuclear cells of one healthy female donor
Du M et al. Derivation of a human induced pluripotent stem cell (hiPSC) line (PUMCSMi001-A) from peripheral blood mononuclear cells of one healthy female donor. . 2021-03-24. Pubmed ID: 33812336; DOI: 10.1016/j.scr.2021.102312 PUMCSMi001-A 2021-03-24 2021-03-24 PubMed: 33812336 DOI: 10.1016/j.scr.2021.102312Associated cell lines:
-
Duong Phu M, Bross S, Burkhalter MD, Philipp M
Limitations and opportunities in the pharmacotherapy of ciliopathies
Duong Phu M et al. Limitations and opportunities in the pharmacotherapy of ciliopathies. . 2021-03-23. Pubmed ID: 33771583; DOI: 10.1016/j.pharmthera.2021.107841 MHHi016-AMHHi016-B 2021-03-23 2021-03-23 PubMed: 33771583 DOI: 10.1016/j.pharmthera.2021.107841 -
Maneepitasut W, Wongkummool W, Tong-Ngam P, Promthep K, Tubsuwan A, Khine Linn A, Phakdeekitcharoen B, Borwornpinyo S, Kitiyanant N, Phanthong P, Hongeng S
Generation of human induced pluripotent stem cell line (MUi026-A) from a patient with autosomal dominant polycystic kidney disease carrying PKD1 point mutation
Maneepitasut W et al. Generation of human induced pluripotent stem cell line (MUi026-A) from a patient with autosomal dominant polycystic kidney disease carrying PKD1 point mutation. . 2021-03-22. Pubmed ID: 33799277; DOI: 10.1016/j.scr.2021.102306 MUi026-A 2021-03-22 2021-03-22 PubMed: 33799277 DOI: 10.1016/j.scr.2021.102306Associated cell lines:
-
Caengprasath N, Theerapanon T, Porntaveetus T, Shotelersuk V
MBTPS2, a membrane bound protease, underlying several distinct skin and bone disorders
Caengprasath N et al. MBTPS2, a membrane bound protease, underlying several distinct skin and bone disorders. . 2021-03-20. Pubmed ID: 33743732; DOI: 10.1186/s12967-021-02779-5; PMC: PMC7981912 MDCUi001-AMDCUi001-B 2021-03-20 2021-03-20 PubMed: 33743732 DOI: 10.1186/s12967-021-02779-5Associated cell lines:
-
Ma L, Wu Z, Tang Q, Ji X, Mei Y, Peng T, Xu Q, Zhou W, Xiong M
Generation of an induced pluripotent stem cell line from a patient with global development delay carrying DYRK1A mutation (c.1730T>A) and a gene correction isogenic iPSC line
Ma L et al. Generation of an induced pluripotent stem cell line from a patient with global development delay carrying DYRK1A mutation (c.1730T>A) and a gene correction isogenic iPSC line. . 2021-03-20. Pubmed ID: 33813175; DOI: 10.1016/j.scr.2021.102305 FDCHi005-AFDCHi005-B 2021-03-20 2021-03-20 PubMed: 33813175 DOI: 10.1016/j.scr.2021.102305Associated cell lines:
-
Devito LG, Healy L, Mohammed S, Guillemot F, Dias C
Generation of an iPSC line (CRICKi001-A) from an individual with a germline SMARCA4 missense mutation and autism spectrum disorder
Devito LG et al. Generation of an iPSC line (CRICKi001-A) from an individual with a germline SMARCA4 missense mutation and autism spectrum disorder. . 2021-03-20. Pubmed ID: 33799280; DOI: 10.1016/j.scr.2021.102304 KCLi001-ACRICKi001-A 2021-03-20 2021-03-20 PubMed: 33799280 DOI: 10.1016/j.scr.2021.102304Associated cell lines:
-
Sun C, Li B, Yang M, Guo R, Yuan S, Wang J, Hu H
Generation of GPAM knockout human embryonic stem cell line SYSUe-008-A using CRISPR/Cas9
Sun C et al. Generation of GPAM knockout human embryonic stem cell line SYSUe-008-A using CRISPR/Cas9. . 2021-03-19. Pubmed ID: 33831647; DOI: 10.1016/j.scr.2021.102303 SYSUe008-A 2021-03-19 2021-03-19 PubMed: 33831647 DOI: 10.1016/j.scr.2021.102303Associated cell lines:
-
Calado SM, Bento D, Justino D, Mendes-Silva L, Marques N, Bragança J
Generation of a human induced pluripotent stem cell line (UALGi001-A) from a patient with Left-Ventricular Noncompaction Cardiomyopathy
Calado SM et al. Generation of a human induced pluripotent stem cell line (UALGi001-A) from a patient with Left-Ventricular Noncompaction Cardiomyopathy. . 2021-03-19. Pubmed ID: 33799278; DOI: 10.1016/j.scr.2021.102302 UALGi001-A 2021-03-19 2021-03-19 PubMed: 33799278 DOI: 10.1016/j.scr.2021.102302Associated cell lines:
-
Wang D, Lin J, Jin M, Wang N
Establishment of a human iPSC line XMDYYYi001-A from a patient with Becker muscular dystrophy harboring duplications of exons 2-19 in dystrophin gene
Wang D et al. Establishment of a human iPSC line XMDYYYi001-A from a patient with Becker muscular dystrophy harboring duplications of exons 2-19 in dystrophin gene. . 2021-03-18. Pubmed ID: 33799273; DOI: 10.1016/j.scr.2021.102298 XMDYYYi001-A 2021-03-18 2021-03-18 PubMed: 33799273 DOI: 10.1016/j.scr.2021.102298Associated cell lines:
-
Cañibano-Hernández A, Valdes-Sanchez L, Garcia-Delgado AB, Ponte-Zúñiga B, Diaz-Corrales FJ, de la Cerda B
Generation of the human iPSC line ESi082-A from a patient with macular dystrophy associated to mutations in the CRB1 gene
Cañibano-Hernández A et al. Generation of the human iPSC line ESi082-A from a patient with macular dystrophy associated to mutations in the CRB1 gene. . 2021-03-18. Pubmed ID: 33773389; DOI: 10.1016/j.scr.2021.102301 ESi082-A 2021-03-18 2021-03-18 PubMed: 33773389 DOI: 10.1016/j.scr.2021.102301Associated cell lines:
-
Pichard L, Brondello JM, Becker F, Desprat R, De Ceuninck F, Pastoureau P, Noel D, Jorgensen C, Lemaitre JM
Establishment of a collection of human pluripotent stem cell lines (iPSC) from mesenchymal stem cells (MSC) from three healthy elderly donors
Pichard L et al. Establishment of a collection of human pluripotent stem cell lines (iPSC) from mesenchymal stem cells (MSC) from three healthy elderly donors. . 2021-03-18. Pubmed ID: 33780731; DOI: 10.1016/j.scr.2021.102297 REGUi012-AREGUi013-AREGUi014-A 2021-03-18 2021-03-18 PubMed: 33780731 DOI: 10.1016/j.scr.2021.102297Associated cell lines:
-
Magusali Naciye, Graham Andrew C., Piers Thomas M., Panichnantakul Pantila, Yaman Umran, Shoai Maryam, Reynolds Regina H., Botia Juan A., Brookes Keeley J., Guetta-Baranes Tamar, Bellou Eftychia, Bayram Sevinc, Sokolova Dimitra, Ryten Mina, Frigerio Carlo Sala, Escott-Price Valentina, Morgan Kevin, Pocock Jennifer M., Hardy John, Salih Dervis A.
Genetic variability associated with OAS1 expression in myeloid cells increases the risk of Alzheimer’s disease and severe COVID-19 outcomes
Magusali Naciye et al. Genetic variability associated with OAS1 expression in myeloid cells increases the risk of Alzheimer’s disease and severe COVID-19 outcomes. . 2021-03-18. DOI: 10.1101/2021.03.16.435702 BIONi010-C 2021-03-18 2021-03-18 DOI: 10.1101/2021.03.16.435702Associated cell lines:
-
Wen J, He C, Feng Y, Song J, Liu J, Liu X, Mei L, Ling J, Chen H, Liu Y
Establishment of an iPSC line (CSUXHi004-A) from a patient with Waardenburg syndrome type I caused by a PAX3 splice mutation
Wen J et al. Establishment of an iPSC line (CSUXHi004-A) from a patient with Waardenburg syndrome type I caused by a PAX3 splice mutation. . 2021-03-18. Pubmed ID: 33774334; DOI: 10.1016/j.scr.2021.102300 CSUXHi004-A 2021-03-18 2021-03-18 PubMed: 33774334 DOI: 10.1016/j.scr.2021.102300Associated cell lines:
-
He L, Han X, Zhao H, Li S, Chen Z, Wang C, Wang S, Peng L, Deng W, Li Z, Tang B, Jiang H
Generation of spinocerebellar ataxia type 3 patient-derived induced pluripotent stem cell line (CSUXHi005-A) from human urine epithelial cells
He L et al. Generation of spinocerebellar ataxia type 3 patient-derived induced pluripotent stem cell line (CSUXHi005-A) from human urine epithelial cells. . 2021-03-17. Pubmed ID: 33761381; DOI: 10.1016/j.scr.2021.102289 CSUXHi002-ACSUXHi005-A 2021-03-17 2021-03-17 PubMed: 33761381 DOI: 10.1016/j.scr.2021.102289Associated cell lines:
-
Yuan F, Wang S, Wang Y, Wang A, Wang C, Luo X, Xu Q, Yin R, Cheng H, Wang C, Guo M, Zhang Y, Xi J, Yang J, Sun X, Yan J, Zeng F, Chen Y
Generation and characterization of the induced pluripotent stem cell line SHCDNi004-A from a ten-year-old Chinese boy with X-linked mental retardation in IL1RAPL1 deficiency
Yuan F et al. Generation and characterization of the induced pluripotent stem cell line SHCDNi004-A from a ten-year-old Chinese boy with X-linked mental retardation in IL1RAPL1 deficiency. . 2021-03-17. Pubmed ID: 33774333; DOI: 10.1016/j.scr.2021.102292 SHCDNi004-A 2021-03-17 2021-03-17 PubMed: 33774333 DOI: 10.1016/j.scr.2021.102292Associated cell lines:
-
Qian R, Wang L, Chen H, Ding Y, Wang D, Chen C, Chu M, Shan X, Guo X
Establishment of a human induced pluripotent stem cell line (WMUi031-A) from a Lowe syndrome patient carrying a OCRL gene mutation (c.2626dupA)
Qian R et al. Establishment of a human induced pluripotent stem cell line (WMUi031-A) from a Lowe syndrome patient carrying a OCRL gene mutation (c.2626dupA). . 2021-03-17. Pubmed ID: 33765594; DOI: 10.1016/j.scr.2021.102294 WMUi031-A 2021-03-17 2021-03-17 PubMed: 33765594 DOI: 10.1016/j.scr.2021.102294Associated cell lines:
-
Wu H, Wang G, Gao E, Zhao J, Zhang L, Chen L, Zhu Y, Zhang J, Liu Z
Generation of the induced pluripotent stem cell line (NCKDi002-A) from a 22-year-old patient with Focal Segmental Glomerular Sclerosis carrying a heterozygous mutation in WT1 gene
Wu H et al. Generation of the induced pluripotent stem cell line (NCKDi002-A) from a 22-year-old patient with Focal Segmental Glomerular Sclerosis carrying a heterozygous mutation in WT1 gene. . 2021-03-17. Pubmed ID: 33780729; DOI: 10.1016/j.scr.2021.102293 NCKDi002-A 2021-03-17 2021-03-17 PubMed: 33780729 DOI: 10.1016/j.scr.2021.102293Associated cell lines:
-
Fukunaga I, Oe Y, Danzaki K, Ohta S, Chen C, Iizumi M, Shiga T, Matsuoka R, Anzai T, Hibiya-Motegi R, Tajima S, Ikeda K, Akamatsu W, Kamiya K
Generation of two iPSC lines from siblings of a homozygous patient with hearing loss and a heterozygous carrier with normal hearing carrying p.G45E/Y136X mutation in GJB2
Fukunaga I et al. Generation of two iPSC lines from siblings of a homozygous patient with hearing loss and a heterozygous carrier with normal hearing carrying p.G45E/Y136X mutation in GJB2. . 2021-03-16. Pubmed ID: 33780732; DOI: 10.1016/j.scr.2021.102290 JUFMDOi001-AJUFMDOi002-A 2021-03-16 2021-03-16 PubMed: 33780732 DOI: 10.1016/j.scr.2021.102290Associated cell lines:
-
Yuzuriha A, Nakamura S, Sugimoto N, Kihara S, Nakagawa M, Yamamoto T, Sekiguchi K, Eto K
Extracellular laminin regulates hematopoietic potential of pluripotent stem cells through integrin β1-ILK-β-catenin-JUN axis
Yuzuriha A et al. Extracellular laminin regulates hematopoietic potential of pluripotent stem cells through integrin β1-ILK-β-catenin-JUN axis. . 2021-03-16. Pubmed ID: 33813173; DOI: 10.1016/j.scr.2021.102287 KUIMSe003-AKUIMSe004-A 2021-03-16 2021-03-16 PubMed: 33813173 DOI: 10.1016/j.scr.2021.102287Associated cell lines:
-
Srivastava A, Lester Sequiera G, Narayan Alagarsamy K, Rockman-Greenberg C, Dhingra S
Generation of human induced pluripotent stem cell (hiPSC) line UOMi005-A from PBMCs of a patient with Kearns-Sayre syndrome
Srivastava A et al. Generation of human induced pluripotent stem cell (hiPSC) line UOMi005-A from PBMCs of a patient with Kearns-Sayre syndrome. . 2021-03-16. Pubmed ID: 33756177; DOI: 10.1016/j.scr.2021.102283 UOMi001-AUOMi002-AUOMi005-A 2021-03-16 2021-03-16 PubMed: 33756177 DOI: 10.1016/j.scr.2021.102283 -
Li Y, Li J, Zhou T, Pan G, Huang K
Generation of PARP1 gene knockout human embryonic stem cell line using CRISPR/Cas9
Li Y et al. Generation of PARP1 gene knockout human embryonic stem cell line using CRISPR/Cas9. . 2021-03-13. Pubmed ID: 33740642; DOI: 10.1016/j.scr.2021.102288 WAe001-A-63 2021-03-13 2021-03-13 PubMed: 33740642 DOI: 10.1016/j.scr.2021.102288Associated cell lines:
-
Zhang XH, Xie Y, Xu K, Li Y
Generation of an induced pluripotent stem cell line BIOi002-A from a patient with autosomal dominant optic atrophy
Zhang XH et al. Generation of an induced pluripotent stem cell line BIOi002-A from a patient with autosomal dominant optic atrophy. . 2021-03-13. Pubmed ID: 33752025; DOI: 10.1016/j.scr.2021.102278 BIOi002-A 2021-03-13 2021-03-13 PubMed: 33752025 DOI: 10.1016/j.scr.2021.102278Associated cell lines:
-
Jahng JWS, Black KE, Liu L, Bae HR, Perez M, Ashley EA, Sallam K, Wu JC
Generation of three induced pluripotent stem cell lines, SCVIi003-A, SCVIi004-A, SCVIi005-A, from patients with ARVD/C caused by heterozygous mutations in the PKP2 gene
Jahng JWS et al. Generation of three induced pluripotent stem cell lines, SCVIi003-A, SCVIi004-A, SCVIi005-A, from patients with ARVD/C caused by heterozygous mutations in the PKP2 gene. . 2021-03-12. Pubmed ID: 33743362; DOI: 10.1016/j.scr.2021.102284 SCVIi003-ASCVIi004-ASCVIi005-A 2021-03-12 2021-03-12 PubMed: 33743362 DOI: 10.1016/j.scr.2021.102284Associated cell lines:
-
Wang Y, Sun H, Wang Z, Zhang Q, Yang J, Liu Y, Liu H, Shi C, Wang Y, Xu Y
Generation of induced pluripotent stem cell line (ZZUi019-A) derived from skin fibroblasts from a healthy volunteer
Wang Y et al. Generation of induced pluripotent stem cell line (ZZUi019-A) derived from skin fibroblasts from a healthy volunteer. . 2021-03-12. Pubmed ID: 33740644; DOI: 10.1016/j.scr.2021.102285 ZZUi005-AZZUi019-A 2021-03-12 2021-03-12 PubMed: 33740644 DOI: 10.1016/j.scr.2021.102285 -
Zhang L, Ren Q, Liu X, Liu G, Meng S, Xiahou K, Zhang Y, Jiang N, Zhou W
Generation of induced pluripotent stem cell line (IPTi002-A) from an 87-year old sporadic Alzheimer's disease patient with APOE3 (ε3/ε3) genotype
Zhang L et al. Generation of induced pluripotent stem cell line (IPTi002-A) from an 87-year old sporadic Alzheimer's disease patient with APOE3 (ε3/ε3) genotype. . 2021-03-12. Pubmed ID: 33799279; DOI: 10.1016/j.scr.2021.102282 IPTi002-A 2021-03-12 2021-03-12 PubMed: 33799279 DOI: 10.1016/j.scr.2021.102282Associated cell lines:
-
Kong D, Feng B, Amponsah AE, He J, Guo R, Liu B, Du X, Liu X, Zhang S, Lv F, Ma J, Cui H
hiPSC-derived NSCs effectively promote the functional recovery of acute spinal cord injury in mice
Kong D et al. hiPSC-derived NSCs effectively promote the functional recovery of acute spinal cord injury in mice. . 2021-03-11. Pubmed ID: 33706803; DOI: 10.1186/s13287-021-02217-9; PMC: PMC7953804 HEBHMUi002-A 2021-03-11 2021-03-11 PubMed: 33706803 DOI: 10.1186/s13287-021-02217-9Associated cell lines:
-
Liu L, Shenoy SP, Jahng JWS, Liu Y, Knowles JW, Zhuge Y, Wu JC
Generation of two heterozygous MYBPC3 mutation-carrying human iPSC lines, SCVIi001-A and SCVIi002-A, for modeling hypertrophic cardiomyopathy
Liu L et al. Generation of two heterozygous MYBPC3 mutation-carrying human iPSC lines, SCVIi001-A and SCVIi002-A, for modeling hypertrophic cardiomyopathy. . 2021-03-11. Pubmed ID: 33743363; DOI: 10.1016/j.scr.2021.102279 SCVIi001-ASCVIi002-A 2021-03-11 2021-03-11 PubMed: 33743363 DOI: 10.1016/j.scr.2021.102279Associated cell lines:
-
Guo X, Qian R, Shan X, Yang L, Chen H, Ding Y, Chen C, Chu M, Lin J, Wang D
Generation of a human induced pluripotent stem cell line (WMUi021-A) from a Gitelman syndrome patient carrying a SLC12A3 gene mutation (c.179C > T)
Guo X et al. Generation of a human induced pluripotent stem cell line (WMUi021-A) from a Gitelman syndrome patient carrying a SLC12A3 gene mutation (c.179C > T). . 2021-03-11. Pubmed ID: 33735743; DOI: 10.1016/j.scr.2021.102280 WMUi021-A 2021-03-11 2021-03-11 PubMed: 33735743 DOI: 10.1016/j.scr.2021.102280Associated cell lines:
-
Lester Sequiera G, Srivastava A, Alagarsamy KN, Rockman-Greenberg C, Dhingra S
Generation and Evaluation of Isogenic iPSC as a Source of Cell Replacement Therapies in Patients with Kearns Sayre Syndrome
Lester Sequiera G et al. Generation and Evaluation of Isogenic iPSC as a Source of Cell Replacement Therapies in Patients with Kearns Sayre Syndrome. . 2021-03-05. Pubmed ID: 33807701; DOI: 10.3390/cells10030568; PMC: PMC7998189 UOMi005-AUOMi006-A 2021-03-05 2021-03-05 PubMed: 33807701 DOI: 10.3390/cells10030568 -
Diakatou M, Dubois G, Erkilic N, Sanjurjo-Soriano C, Meunier I, Kalatzis V
Allele-Specific Knockout by CRISPR/Cas to Treat Autosomal Dominant Retinitis Pigmentosa Caused by the G56R Mutation in NR2E3
Diakatou M et al. Allele-Specific Knockout by CRISPR/Cas to Treat Autosomal Dominant Retinitis Pigmentosa Caused by the G56R Mutation in NR2E3. . 2021-03-05. Pubmed ID: 33807610; DOI: 10.3390/ijms22052607; PMC: PMC7961898 INMi003-AINMi004-A 2021-03-05 2021-03-05 PubMed: 33807610 DOI: 10.3390/ijms22052607 -
Chen PF, Chen T, Forman TE, Swanson AC, O'Kelly B, Dwyer SA, Buttermore ED, Kleiman R, Js Carrington S, Lavery DJ, Swanson LC, Olson HE, Sahin M
Generation and characterization of human induced pluripotent stem cells (iPSCs) from three male and three female patients with CDKL5 Deficiency Disorder (CDD)
Chen PF et al. Generation and characterization of human induced pluripotent stem cells (iPSCs) from three male and three female patients with CDKL5 Deficiency Disorder (CDD). . 2021-03-05. Pubmed ID: 33714067; DOI: 10.1016/j.scr.2021.102276 BCHi001-ABCHi001-BBCHi002-ABCHi003-ABCHi003-BBCHi004-ABCHi004-BBCHi005-ABCHi005-BBCHi006-ABCHi006-B 2021-03-05 2021-03-05 PubMed: 33714067 DOI: 10.1016/j.scr.2021.102276 -
Wu J, Ren J, Luo H, Zuo X, Tang Y
Generation of patient-specific induced pluripotent stem cell line (CSUi002-A) from a patient with isolated dystonia carrying TOR1A mutation
Wu J et al. Generation of patient-specific induced pluripotent stem cell line (CSUi002-A) from a patient with isolated dystonia carrying TOR1A mutation. . 2021-03-04. Pubmed ID: 33706202; DOI: 10.1016/j.scr.2021.102277 CSUi002-A 2021-03-04 2021-03-04 PubMed: 33706202 DOI: 10.1016/j.scr.2021.102277Associated cell lines:
-
Nilsri N, Jangprasert P, Pawinwongchai J, Israsena N, Rojnuckarin P
Distinct effects of V617F and exon12-mutated JAK2 expressions on erythropoiesis in a human induced pluripotent stem cell (iPSC)-based model
Nilsri N et al. Distinct effects of V617F and exon12-mutated JAK2 expressions on erythropoiesis in a human induced pluripotent stem cell (iPSC)-based model. . 2021-03-04. Pubmed ID: 33664283; DOI: 10.1038/s41598-021-83895-6; PMC: PMC7933160 ASUi001-AASUi002-A 2021-03-04 2021-03-04 PubMed: 33664283 DOI: 10.1038/s41598-021-83895-6 -
Liu M, Li X, Fu W, Wang M, Liu Y, Wang L, Hu L, Zhao X, Dong J
Induced pluripotent stem cell (iPSC) line (ZZUNEUi009-A) from a healthy female individual
Liu M et al. Induced pluripotent stem cell (iPSC) line (ZZUNEUi009-A) from a healthy female individual. . 2021-03-03. Pubmed ID: 33730648; DOI: 10.1016/j.scr.2021.102275 ZZUNEUi009-A 2021-03-03 2021-03-03 PubMed: 33730648 DOI: 10.1016/j.scr.2021.102275Associated cell lines:
-
Hornig NC, Holterhus PM
Molecular basis of androgen insensitivity syndromes
Hornig NC et al. Molecular basis of androgen insensitivity syndromes. . 2021-03-01. Pubmed ID: 33385475; DOI: 10.1016/j.mce.2020.111146 SKLRMi001-A 2021-03-01 2021-03-01 PubMed: 33385475 DOI: 10.1016/j.mce.2020.111146Associated cell lines:
-
Rabinski T, Sagiv ST, Hausman-Kedem M, Fattal-Valevski A, Rubinstein M, Avraham KB, Vatine GD
Reprogramming of two induced pluripotent stem cell lines from a heterozygous GRIN2D developmental and epileptic encephalopathy (DEE) patient (BGUi011-A) and from a healthy family relative (BGUi012-A)
Rabinski T et al. Reprogramming of two induced pluripotent stem cell lines from a heterozygous GRIN2D developmental and epileptic encephalopathy (DEE) patient (BGUi011-A) and from a healthy family relative (BGUi012-A). . 2021-03-00. Pubmed ID: 33482465; DOI: 10.1016/j.scr.2021.102178 BGUi001-ABGUi002-ABGUi003-ABGUi004-ABGUi005-ABGUi011-ABGUi012-A 2021-03-00 2021-03-00 PubMed: 33482465 DOI: 10.1016/j.scr.2021.102178 -
Abdelalim EM
Modeling different types of diabetes using human pluripotent stem cells
Abdelalim EM. Modeling different types of diabetes using human pluripotent stem cells. . 2021-03-00. Pubmed ID: 33242105; DOI: 10.1007/s00018-020-03710-9 QBRIi007-A 2021-03-00 2021-03-00 PubMed: 33242105 DOI: 10.1007/s00018-020-03710-9Associated cell lines:
-
Chen H, Ding Y, Zhou W, Li J, Qian W, Zhang Z, Li C, Tong H, Rong X, Chu M, Chen C, Wang D, Guo X
Establishment of an induced pluripotent stem cell line (WMUi016-A) from a patient with X-linked Dent disease (X-Dent) carrying the hemizygote mutation p.R718* (c.2152C > T) in the CLCN5 gene
Chen H et al. Establishment of an induced pluripotent stem cell line (WMUi016-A) from a patient with X-linked Dent disease (X-Dent) carrying the hemizygote mutation p.R718* (c.2152C > T) in the CLCN5 gene. . 2021-03-00. Pubmed ID: 33545640; DOI: 10.1016/j.scr.2021.102209 WMUi016-A 2021-03-00 2021-03-00 PubMed: 33545640 DOI: 10.1016/j.scr.2021.102209Associated cell lines:
-
Karthik R, Menaka R, Hariharan M, Won D
Ischemic Lesion Segmentation using Ensemble of Multi-Scale Region Aligned CNN
Karthik R et al. Ischemic Lesion Segmentation using Ensemble of Multi-Scale Region Aligned CNN. . 2021-03-00. Pubmed ID: 33223277; DOI: 10.1016/j.cmpb.2020.105831 ZJUi005-A 2021-03-00 2021-03-00 PubMed: 33223277 DOI: 10.1016/j.cmpb.2020.105831Associated cell lines:
-
Meng-Jie L.
Application progress of induced pluripotent stem cells in Alzheimer's disease
Meng-Jie L.. Application progress of induced pluripotent stem cells in Alzheimer's disease. . 2021-02-28. DOI: 10.11855/j.issn.0577-7402.2021.02.14 IMEDEAi006-A 2021-02-28 2021-02-28 DOI: 10.11855/j.issn.0577-7402.2021.02.14Associated cell lines:
-
Liu X, Liu Y, Ma Y, Gong Y, Liu Q, Sun W, Guo H
Establishment of patient-specific induced pluripotent stem cell line SDUBMSi009-A from a patient with X-linked Lowe syndrome
Liu X et al. Establishment of patient-specific induced pluripotent stem cell line SDUBMSi009-A from a patient with X-linked Lowe syndrome. . 2021-03-00. Pubmed ID: 33540283; DOI: 10.1016/j.scr.2021.102171 SDUBMSi009-A 2021-03-00 2021-03-00 PubMed: 33540283 DOI: 10.1016/j.scr.2021.102171Associated cell lines:
-
Guo J, Di W, Zhang W, Dai Q, Zhao J, Deng Y, Wang Y
Generation of an induced pluripotent stem cell line (SIAISi009-A) from a 60-year-old Chinese Han female with mild cognitive impairment (MCI) having two copies of APOE4/4 allele
Guo J et al. Generation of an induced pluripotent stem cell line (SIAISi009-A) from a 60-year-old Chinese Han female with mild cognitive impairment (MCI) having two copies of APOE4/4 allele. . 2021-03-00. Pubmed ID: 33524675; DOI: 10.1016/j.scr.2021.102198 SIAISi009-A 2021-03-00 2021-03-00 PubMed: 33524675 DOI: 10.1016/j.scr.2021.102198Associated cell lines:
-
Fan L, Mao C, Shi C, Fan Y, Liu F, Zheng H, Su Y, Liu H, Wang Y, Liu YT, Yang J, Xu Y
Generation of an induced pluripotent stem cell line (ZZUi022-A) from a paroxysmal kinesigenic dyskinesia individual carrying the PRRT2 gene mutation
Fan L et al. Generation of an induced pluripotent stem cell line (ZZUi022-A) from a paroxysmal kinesigenic dyskinesia individual carrying the PRRT2 gene mutation. . 2021-03-00. Pubmed ID: 33550051; DOI: 10.1016/j.scr.2021.102210 ZZUi022-A 2021-03-00 2021-03-00 PubMed: 33550051 DOI: 10.1016/j.scr.2021.102210Associated cell lines:
-
Zhang D, McLenachan S, Chen SC, Zaw K, Alziyadat Y, Zhang X, Lamey TM, Thompson JA, McLaren TL, Mellough C, De Roach JN, Chen FK
Generation of two induced pluripotent stem cell lines from a patient with recessive inherited retinal disease caused by compound heterozygous mutations in SNRNP200
Zhang D et al. Generation of two induced pluripotent stem cell lines from a patient with recessive inherited retinal disease caused by compound heterozygous mutations in SNRNP200. . 2021-03-00. Pubmed ID: 33429167; DOI: 10.1016/j.scr.2020.102154 LEIi015-ALEIi015-B 2021-03-00 2021-03-00 PubMed: 33429167 DOI: 10.1016/j.scr.2020.102154 -
Kim J, Koh H, Zhen X, Lee DS, Ha HY, Lee JH
Establishment of iPSC (KRIBBi001-A) from CD34+ group O D-negative bone marrow blood
Kim J et al. Establishment of iPSC (KRIBBi001-A) from CD34+ group O D-negative bone marrow blood. . 2021-03-00. Pubmed ID: 33529979; DOI: 10.1016/j.scr.2021.102199 KRIBBi001-A 2021-03-00 2021-03-00 PubMed: 33529979 DOI: 10.1016/j.scr.2021.102199Associated cell lines:
-
Hanss Z, Larsen SB, Antony P, Mencke P, Massart F, Jarazo J, Schwamborn JC, Barbuti PA, Mellick GD, Krüger R
Mitochondrial and Clearance Impairment in p.D620N VPS35 Patient-Derived Neurons
Hanss Z et al. Mitochondrial and Clearance Impairment in p.D620N VPS35 Patient-Derived Neurons. . 2021-03-00. Pubmed ID: 33142012; DOI: 10.1002/mds.28365 LCSBi001-A 2021-03-00 2021-03-00 PubMed: 33142012 DOI: 10.1002/mds.28365Associated cell lines:
-
Hou C, Liu W, Xie L, Zheng J, Chen X, Sun X, Zhang Y, Xu M, Li Y, Xiao T
Generation of an induced pluripotent stem cell line from a Chinese Han child with arrhythmia
Hou C et al. Generation of an induced pluripotent stem cell line from a Chinese Han child with arrhythmia. . 2021-03-00. Pubmed ID: 33497884; DOI: 10.1016/j.scr.2021.102183 SHETi002-A 2021-03-00 2021-03-00 PubMed: 33497884 DOI: 10.1016/j.scr.2021.102183Associated cell lines:
-
Hou C, Xie L, Qiu Q, Lin H, Liu W, Sun X, Zhang Y, Xu M, Li Y, Xiao T
Generation of an induced pluripotent stem cell line from a Chinese Han infant with floating-harbor syndrome accompanied with dilated cardiomyopathy
Hou C et al. Generation of an induced pluripotent stem cell line from a Chinese Han infant with floating-harbor syndrome accompanied with dilated cardiomyopathy. . 2021-03-00. Pubmed ID: 33517121; DOI: 10.1016/j.scr.2021.102182 SHETi001-A 2021-03-00 2021-03-00 PubMed: 33517121 DOI: 10.1016/j.scr.2021.102182Associated cell lines:
-
Guo Xiaoling, Qian Rengcheng, Yang Liang, Chen Huihui, Ding Yinjuan, Shan Xiaoou, Chen Congde, Ni Wenfei, Lin Jian, Chu Maoping
Establishment of an induced pluripotent stem cell line from a Noonan syndrome patient with the heterozygote mutation p.S257L (c.770C>T) in RAF1 gene
Guo Xiaoling et al. Establishment of an induced pluripotent stem cell line from a Noonan syndrome patient with the heterozygote mutation p.S257L (c.770C>T) in RAF1 gene. . 2021-03-00. DOI: 10.1016/j.scr.2021.102281 WMUi022-A 2021-03-00 2021-03-00 DOI: 10.1016/j.scr.2021.102281Associated cell lines:
-
Yang X, Wu F, Zhong J, Li F
Establishment of human embryonic stem cell WAe009-A-48 carrying a long QT syndrome mutation in SCN5A
Yang X et al. Establishment of human embryonic stem cell WAe009-A-48 carrying a long QT syndrome mutation in SCN5A. . 2021-03-00. Pubmed ID: 33517120; DOI: 10.1016/j.scr.2021.102194 WAe009-AWAe009-A-48 2021-03-00 2021-03-00 PubMed: 33517120 DOI: 10.1016/j.scr.2021.102194Associated cell lines:
-
Wen J, Song J, He C, Ling J, Liu Y, Chen H, Gong W, Mei L, Feng Y
Establishment of an iPSC line (CSUXHi003-A) from a patient with Waardenburg syndrome type Ⅱ caused by a MITF mutation
Wen J et al. Establishment of an iPSC line (CSUXHi003-A) from a patient with Waardenburg syndrome type Ⅱ caused by a MITF mutation. . 2021-03-00. Pubmed ID: 33454628; DOI: 10.1016/j.scr.2021.102157 JTUi002-ACSUXHi003-A 2021-03-00 2021-03-00 PubMed: 33454628 DOI: 10.1016/j.scr.2021.102157Associated cell lines:
-
Madrid M, Sumen C, Aivio S, Saklayen N
Autologous Induced Pluripotent Stem Cell-Based Cell Therapies: Promise, Progress, and Challenges
Madrid M et al. Autologous Induced Pluripotent Stem Cell-Based Cell Therapies: Promise, Progress, and Challenges. . 2021-03-00. Pubmed ID: 33725407; DOI: 10.1002/cpz1.88 NYGCe001-A 2021-03-00 2021-03-00 PubMed: 33725407 DOI: 10.1002/cpz1.88Associated cell lines:
-
Xu M, Wang L, Yin J, Xiong J, Guo Q, Yang W
Establishment of an induced pluripotent stem cell line (SAHGMUi001-A) from a patient with Netherton syndrome carrying SPINK5 mutation
Xu M et al. Establishment of an induced pluripotent stem cell line (SAHGMUi001-A) from a patient with Netherton syndrome carrying SPINK5 mutation. . 2021-03-00. Pubmed ID: 33556917; DOI: 10.1016/j.scr.2021.102213 SAHGMUi001-A 2021-03-00 2021-03-00 PubMed: 33556917 DOI: 10.1016/j.scr.2021.102213Associated cell lines:
-
Zhang W, Hua Y, Di W, Guo J, Dai Q, Zhao J, Zhang B, Wang Y
Generation of a human induced pluripotent stem cell line (SIAISi011-A) from a 61-year-old Chinese Han healthy female donor
Zhang W et al. Generation of a human induced pluripotent stem cell line (SIAISi011-A) from a 61-year-old Chinese Han healthy female donor. . 2021-03-00. Pubmed ID: 33465532; DOI: 10.1016/j.scr.2021.102173 SIAISi011-A 2021-03-00 2021-03-00 PubMed: 33465532 DOI: 10.1016/j.scr.2021.102173Associated cell lines:
-
Sahabian A, Dahlmann J, Martin U, Olmer R
Production and cryopreservation of definitive endoderm from human pluripotent stem cells under defined and scalable culture conditions
Sahabian A et al. Production and cryopreservation of definitive endoderm from human pluripotent stem cells under defined and scalable culture conditions. . 2021-03-00. Pubmed ID: 33580232; DOI: 10.1038/s41596-020-00470-5 MHHi006-AMHHi006-A-4 2021-03-00 2021-03-00 PubMed: 33580232 DOI: 10.1038/s41596-020-00470-5Associated cell lines:
-
Yang X, Liu N, Mu H, Lv Y, Zhang H, Li Y, Guan J, Gai Z, Liu Y
Reprogramming of human peripheral blood mononuclear cell (PBMC) from a patient suffering from hearing loss into iPSC line (SDQLCHi035-A) maintaining compound heterozygous variations in GJB2 gene
Yang X et al. Reprogramming of human peripheral blood mononuclear cell (PBMC) from a patient suffering from hearing loss into iPSC line (SDQLCHi035-A) maintaining compound heterozygous variations in GJB2 gene. . 2021-03-00. Pubmed ID: 33517119; DOI: 10.1016/j.scr.2021.102188 SDQLCHi035-A 2021-03-00 2021-03-00 PubMed: 33517119 DOI: 10.1016/j.scr.2021.102188Associated cell lines:
-
Wang B, Yang L, Li Y, Gao M, Zhang H, Yang X, Guan J, Liu Y, Gai Z
Establishment of a human induced pluripotent stem cell line (SDQLCHi037-A) from a patient with Alagille syndrome carrying heterozygous mutation in JAG1 gene
Wang B et al. Establishment of a human induced pluripotent stem cell line (SDQLCHi037-A) from a patient with Alagille syndrome carrying heterozygous mutation in JAG1 gene. . 2021-03-00. Pubmed ID: 33465531; DOI: 10.1016/j.scr.2021.102162 SDQLCHi037-A 2021-03-00 2021-03-00 PubMed: 33465531 DOI: 10.1016/j.scr.2021.102162Associated cell lines:
-
Qin Z, Sun L, Sun X, Gao X, Su H
Reprogramming of a human induced pluripotent stem cell line from a Marfan syndrome patient harboring a heterozygous mutation of c.2939G > A in FBN1 gene
Qin Z et al. Reprogramming of a human induced pluripotent stem cell line from a Marfan syndrome patient harboring a heterozygous mutation of c.2939G > A in FBN1 gene. . 2021-03-00. Pubmed ID: 33450697; DOI: 10.1016/j.scr.2021.102163 ZZUSAHi003-A 2021-03-00 2021-03-00 PubMed: 33450697 DOI: 10.1016/j.scr.2021.102163Associated cell lines:
-
Ou-Yang CH, Tai CH, Lin HY, Huang CY, Lin CH
Generation of a human induced pluripotent stem cell (iPSC) line (IBMS-iPSC-070-02) from a patient with neurodegeneration with brain iron accumulation (NBIA) having compound heterozygous mutations in PANK2 gene
Ou-Yang CH et al. Generation of a human induced pluripotent stem cell (iPSC) line (IBMS-iPSC-070-02) from a patient with neurodegeneration with brain iron accumulation (NBIA) having compound heterozygous mutations in PANK2 gene. . 2021-03-00. Pubmed ID: 33517123; DOI: 10.1016/j.scr.2021.102190 IBMSi025-A 2021-03-00 2021-03-00 PubMed: 33517123 DOI: 10.1016/j.scr.2021.102190Associated cell lines:
-
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:
-
Schnichels S, Paquet-Durand F, Löscher M, Tsai T, Hurst J, Joachim SC, Klettner A
Retina in a dish: Cell cultures, retinal explants and animal models for common diseases of the retina
Schnichels S et al. Retina in a dish: Cell cultures, retinal explants and animal models for common diseases of the retina. . 2021-03-00. Pubmed ID: 32721458; DOI: 10.1016/j.preteyeres.2020.100880 CABi003-A 2021-03-00 2021-03-00 PubMed: 32721458 DOI: 10.1016/j.preteyeres.2020.100880Associated cell lines:
-
Yang Z, Yuan F, Wang N, Liu Y, Zhang J, Wei R, Wu F, Wu Y, You K, Chen Y, Yang F, Li YX
Generation of a DKK1 homozygous knockout human embryonic stem cell line WAe001-A-21 using CRISPR/Cas9
Yang Z et al. Generation of a DKK1 homozygous knockout human embryonic stem cell line WAe001-A-21 using CRISPR/Cas9. . 2021-03-00. Pubmed ID: 33461039; DOI: 10.1016/j.scr.2021.102161 WAe001-AWAe001-A-21 2021-03-00 2021-03-00 PubMed: 33461039 DOI: 10.1016/j.scr.2021.102161Associated cell lines:
-
Zhao T, Bai R, Wu F, Lu WJ, Zhang J
Generation of a TBX5 homozygous knockout embryonic stem cell line (WAe009-A-45) by CRISPR/Cas9 genome editing
Zhao T et al. Generation of a TBX5 homozygous knockout embryonic stem cell line (WAe009-A-45) by CRISPR/Cas9 genome editing. . 2021-03-00. Pubmed ID: 33497883; DOI: 10.1016/j.scr.2021.102156 WAe009-AWAe009-A-45 2021-03-00 2021-03-00 PubMed: 33497883 DOI: 10.1016/j.scr.2021.102156Associated cell lines:
-
Liu Y, Li X, Fu W, Liu M, Wang M, Hu L, Wang L, Zhao X, Ding Z, Dong J
An induced pluripotent stem cells line (ZZUNEUi022-A) derived from urine cells of healthy male human
Liu Y et al. An induced pluripotent stem cells line (ZZUNEUi022-A) derived from urine cells of healthy male human. . 2021-03-00. Pubmed ID: 33529980; DOI: 10.1016/j.scr.2021.102191 ZZUNEUi007-AZZUNEUi022-A 2021-03-00 2021-03-00 PubMed: 33529980 DOI: 10.1016/j.scr.2021.102191Associated cell lines:
-
Yang X, Duan C, Zhang H, Li Y, Guan J, Wang D, Lv Y, Gai Z, Liu Y
Establishment of a non-integrate iPS cell line (SDQLCHi023-A) from a patient with Xq25 microduplication syndrome carrying a 1.3 Mb hemizygote duplication at chrXq25
Yang X et al. Establishment of a non-integrate iPS cell line (SDQLCHi023-A) from a patient with Xq25 microduplication syndrome carrying a 1.3 Mb hemizygote duplication at chrXq25. . 2021-03-00. Pubmed ID: 33493992; DOI: 10.1016/j.scr.2020.102147 SDQLCHi023-A 2021-03-00 2021-03-00 PubMed: 33493992 DOI: 10.1016/j.scr.2020.102147Associated cell lines:
-
Zhang W, Dai Q, Hua Y, Di W, Guo J, Zhao J, Deng Y, Wang Y
Generation of three iPSC cell lines (SIAISi006-A, SIAISi007-A and SIAISi008-A) from a 66-year-old Alzheimer's disease (AD) patient and her two unaffected children from Chinese Han population
Zhang W et al. Generation of three iPSC cell lines (SIAISi006-A, SIAISi007-A and SIAISi008-A) from a 66-year-old Alzheimer's disease (AD) patient and her two unaffected children from Chinese Han population. . 2021-03-00. Pubmed ID: 33472125; DOI: 10.1016/j.scr.2021.102172 SIAISi006-ASIAISi007-ASIAISi008-A 2021-03-00 2021-03-00 PubMed: 33472125 DOI: 10.1016/j.scr.2021.102172Associated cell lines:
-
Kamand M, Forsberg SL, Thomassen M, Ilieva M, Meyer M, Svenningsen ÅF, Michel TM
Establishment of an induced pluripotent stem (iPS) cell line (SDUKIi006-A) from a 21-year old male patient diagnosed with atypical autism disorder
Kamand M et al. Establishment of an induced pluripotent stem (iPS) cell line (SDUKIi006-A) from a 21-year old male patient diagnosed with atypical autism disorder. . 2021-03-00. Pubmed ID: 33524673; DOI: 10.1016/j.scr.2021.102185 SDUKIi002-ASDUKIi006-A 2021-03-00 2021-03-00 PubMed: 33524673 DOI: 10.1016/j.scr.2021.102185Associated cell lines:
-
Ghanami Gashti N, Sadighi Gilani MA, Abbasi M
Sertoli cell-only syndrome: etiology and clinical management
Ghanami Gashti N et al. Sertoli cell-only syndrome: etiology and clinical management. . 2021-03-00. Pubmed ID: 33428073; DOI: 10.1007/s10815-021-02063-x; PMC: PMC7910341 HUSTi002-A 2021-03-00 2021-03-00 PubMed: 33428073 DOI: 10.1007/s10815-021-02063-xAssociated cell lines:
-
Liu N, Yang X, Wang S, Dong R, Li Y, Lv Y, Liu Y, Gai Z
PBMC-derived integration-free iPSCs line SDQLCHi039-A from a patient with X-linked agammaglobulinemia carrying a novel 9-bp in-frame deletion in BTK gene
Liu N et al. PBMC-derived integration-free iPSCs line SDQLCHi039-A from a patient with X-linked agammaglobulinemia carrying a novel 9-bp in-frame deletion in BTK gene. . 2021-03-00. Pubmed ID: 33453577; DOI: 10.1016/j.scr.2021.102165 SDQLCHi039-A 2021-03-00 2021-03-00 PubMed: 33453577 DOI: 10.1016/j.scr.2021.102165Associated cell lines:
-
Zhang H, Zhang H, Ma Y, Lv Y, Gai Z, Liu Y
Generation and characterization of an induced pluripotent stem cell line SDQLCHi018-A from a congenital myasthenic syndrome patient carrying compound heterozygote mutations in RAPSN gene
Zhang H et al. Generation and characterization of an induced pluripotent stem cell line SDQLCHi018-A from a congenital myasthenic syndrome patient carrying compound heterozygote mutations in RAPSN gene. . 2021-03-00. Pubmed ID: 33465529; DOI: 10.1016/j.scr.2021.102160 SDQLCHi018-A 2021-03-00 2021-03-00 PubMed: 33465529 DOI: 10.1016/j.scr.2021.102160Associated cell lines:
-
Graffmann N, Martins S, Ljubikj T, Matte JC, Bohndorf M, Wruck W, Adjaye J
Generation of a Crigler-Najjar Syndrome Type I patient-derived induced pluripotent stem cell line CNS705 (HHUUKDi005-A)
Graffmann N et al. Generation of a Crigler-Najjar Syndrome Type I patient-derived induced pluripotent stem cell line CNS705 (HHUUKDi005-A). . 2021-03-00. Pubmed ID: 33485181; DOI: 10.1016/j.scr.2021.102167 HHUUKDi005-A 2021-03-00 2021-03-00 PubMed: 33485181 DOI: 10.1016/j.scr.2021.102167Associated cell lines:
-
Li D, Hong X, Li W, Meng S, Yu H, Zhang X, Wang C, Samokhvalov IM, Liu D, Tang D, Dai Y
Establishment of an induced pluripotent stem cell line SPHi001-A from a systemic lupus erythematosus patient combined with preeclampsia and psoriasis
Li D et al. Establishment of an induced pluripotent stem cell line SPHi001-A from a systemic lupus erythematosus patient combined with preeclampsia and psoriasis. . 2021-03-00. Pubmed ID: 33516123; DOI: 10.1016/j.scr.2021.102192 SPHi001-A 2021-03-00 2021-03-00 PubMed: 33516123 DOI: 10.1016/j.scr.2021.102192Associated cell lines:
-
He L, Chen Z, Peng L, Tang B, Jiang H
Human stem cell models of polyglutamine diseases: Sources for disease models and cell therapy
He L et al. Human stem cell models of polyglutamine diseases: Sources for disease models and cell therapy. . 2021-03-00. Pubmed ID: 33347831; DOI: 10.1016/j.expneurol.2020.113573 ZZUi004-ALUMCi002-ALUMCi003-AMUSIi004-AHIHCNi002-AICGi007-AIBCHi001-ACSSi008-ACSUXHi002-A 2021-03-00 2021-03-00 PubMed: 33347831 DOI: 10.1016/j.expneurol.2020.113573Associated cell lines:
-
Chen M, Lin SM, Li N, Li Y, Li Y, Zhang L
An induced pluripotent stem cell line (GZHMCi003-A) derived from a fetus with exon 3 heterozygous deletion in RUNX2 gene causing cleidocranial dysplasia
Chen M et al. An induced pluripotent stem cell line (GZHMCi003-A) derived from a fetus with exon 3 heterozygous deletion in RUNX2 gene causing cleidocranial dysplasia. . 2021-03-00. Pubmed ID: 33477036; DOI: 10.1016/j.scr.2021.102166 GZHMCi003-A 2021-03-00 2021-03-00 PubMed: 33477036 DOI: 10.1016/j.scr.2021.102166Associated cell lines:
-
Li Zilong, Zhang Xue, Li Xiaomei, Yang Yanan, Xin Hongmei, Yang Xiaomeng, Liu Ning, Gai Zhongtao, Liu Yi
A non-integrated iPSC line (SDQLCHi042-A) from a boy suffering from familial combined hyperlipidemia with compound heterozygous mutations of lipoprotein lipase gene
Li Zilong et al. A non-integrated iPSC line (SDQLCHi042-A) from a boy suffering from familial combined hyperlipidemia with compound heterozygous mutations of lipoprotein lipase gene. . 2021-03-00. DOI: 10.1016/j.scr.2021.102313 SDQLCHi042-A 2021-03-00 2021-03-00 DOI: 10.1016/j.scr.2021.102313Associated cell lines:
-
Li X, Fu W, Guo G, Liu M, Du W, Zhao J, Liu Y, Wang L, Dong J, Zhao X
A heterozygous MYH7 (c. 2156G > A) mutant human induced pluripotent stem cell line (ZZUNEUi020-A) generated from a patient with hypertrophic cardiomyopathy
Li X et al. A heterozygous MYH7 (c. 2156G > A) mutant human induced pluripotent stem cell line (ZZUNEUi020-A) generated from a patient with hypertrophic cardiomyopathy. . 2021-03-00. Pubmed ID: 33453578; DOI: 10.1016/j.scr.2021.102158 ZZUNEUi020-A 2021-03-00 2021-03-00 PubMed: 33453578 DOI: 10.1016/j.scr.2021.102158Associated cell lines:
-
Dong T, Zhang S, Chang Y, Bai R, Jiang Y, Ma S, Li Y, Jiang HF, Lu WJ
The establishment of a homozygous SNTA1 knockout human embryonic stem cell line (WAe009-A-50) using the CRISPR/Cas9 system
Dong T et al. The establishment of a homozygous SNTA1 knockout human embryonic stem cell line (WAe009-A-50) using the CRISPR/Cas9 system. . 2021-03-00. Pubmed ID: 33524674; DOI: 10.1016/j.scr.2021.102196 WAe009-AWAe009-A-50 2021-03-00 2021-03-00 PubMed: 33524674 DOI: 10.1016/j.scr.2021.102196Associated cell lines:
-
Wang L, Gao B, Mo X, Guo X, Huang J
Generation of an urine-derived induced pluripotent stem cell line from a 6-year old X-linked adrenoleukodystrophy (X-ALD) patient
Wang L et al. Generation of an urine-derived induced pluripotent stem cell line from a 6-year old X-linked adrenoleukodystrophy (X-ALD) patient. . 2021-03-00. Pubmed ID: 33472124; DOI: 10.1016/j.scr.2021.102170 WMUi014-A 2021-03-00 2021-03-00 PubMed: 33472124 DOI: 10.1016/j.scr.2021.102170Associated cell lines:
-
Vitale MR, Zöller JEM, Jansch C, Janz A, Edenhofer F, Klopocki E, van den Hove D, Vanmierlo T, Rivero O, Nadif Kasri N, Ziegler GC, Lesch KP
Generation of induced pluripotent stem cell (iPSC) lines carrying a heterozygous (UKWMPi002-A-1) and null mutant knockout (UKWMPi002-A-2) of Cadherin 13 associated with neurodevelopmental disorders using CRISPR/Cas9
Vitale MR et al. Generation of induced pluripotent stem cell (iPSC) lines carrying a heterozygous (UKWMPi002-A-1) and null mutant knockout (UKWMPi002-A-2) of Cadherin 13 associated with neurodevelopmental disorders using CRISPR/Cas9. . 2021-03-00. Pubmed ID: 33486346; DOI: 10.1016/j.scr.2021.102169 UKWMPi002-AUKWMPi002-A-1UKWMPi002-A-2 2021-03-00 2021-03-00 PubMed: 33486346 DOI: 10.1016/j.scr.2021.102169Associated cell lines:
-
Inzunza J, Arias-Fuenzalida J, Segura-Aguilar J, Nalvarte I, Varshney M
Generation of nonviral integration-free human iPS cell line KISCOi001-A from normal human fibroblasts, under defined xeno-free and feeder-free conditions
Inzunza J et al. Generation of nonviral integration-free human iPS cell line KISCOi001-A from normal human fibroblasts, under defined xeno-free and feeder-free conditions. . 2021-03-00. Pubmed ID: 33517122; DOI: 10.1016/j.scr.2021.102193 KISCOi001-A 2021-03-00 2021-03-00 PubMed: 33517122 DOI: 10.1016/j.scr.2021.102193Associated cell lines:
-
Guo X, Zhang X, Wang L, He L, Ding Y, Chen H, Wang D, Rong X, Shen X, Lin J, Chu M
Generation of an urine-derived induced pluripotent stem cell line WMUi017-A from a X-linked Renpenning syndrome (X-RSY) patient with the hemizygous PQBP1 gene mutation p.P609A (c.1825C>G)
Guo X et al. Generation of an urine-derived induced pluripotent stem cell line WMUi017-A from a X-linked Renpenning syndrome (X-RSY) patient with the hemizygous PQBP1 gene mutation p.P609A (c.1825C>G). . 2021-03-00. Pubmed ID: 33477035; DOI: 10.1016/j.scr.2021.102159 WMUi017-A 2021-03-00 2021-03-00 PubMed: 33477035 DOI: 10.1016/j.scr.2021.102159Associated cell lines:
-
Bono F, Mutti V, Piovani G, Minelli A, Mingardi J, Guglielmi A, Missale C, Gennarelli M, Fiorentini C, Barbon A
Establishment and characterization of induced pluripotent stem cell (iPSCs) line UNIBSi014-A from a healthy female donor
Bono F et al. Establishment and characterization of induced pluripotent stem cell (iPSCs) line UNIBSi014-A from a healthy female donor. . 2021-03-00. Pubmed ID: 33548809; DOI: 10.1016/j.scr.2021.102216 UNIBSi012-AUNIBSi013-AUNIBSi014-A 2021-03-00 2021-03-00 PubMed: 33548809 DOI: 10.1016/j.scr.2021.102216Associated cell lines:
-
Zehravi M, Wahid M, Ashraf J
Episomal reprogramming of Duchenne muscular dystrophy patients derived CD3+ T cells towards induced pluripotent stem cells
Zehravi M et al. Episomal reprogramming of Duchenne muscular dystrophy patients derived CD3+ T cells towards induced pluripotent stem cells. . 2021-03-00. Pubmed ID: 33679927; DOI: 10.12669/pjms.37.2.3388; PMC: PMC7931302 MUSIi011-AMUSIi011-B 2021-03-00 2021-03-00 PubMed: 33679927 DOI: 10.12669/pjms.37.2.3388Associated cell lines:
-
Harding P, Lima Cunha D, Méjécase C, Eintracht J, Toualbi L, Sarkar H, Moosajee M
Generation of human iPSC line (UCLi013-A) from a patient with microphthalmia and aniridia, carrying a heterozygous missense mutation c.372C>A p.(Asn124Lys) in PAX6
Harding P et al. Generation of human iPSC line (UCLi013-A) from a patient with microphthalmia and aniridia, carrying a heterozygous missense mutation c.372C>A p.(Asn124Lys) in PAX6. . 2021-03-00. Pubmed ID: 33524672; DOI: 10.1016/j.scr.2021.102184; PMC: PMC7957338 UCLi013-A 2021-03-00 2021-03-00 PubMed: 33524672 DOI: 10.1016/j.scr.2021.102184Associated cell lines:
-
Cui S, Shin YJ, Ko EJ, Lim SW, Ju JH, Lee KI, Lee JY, Yang CW, Chung BH
Human-induced pluripotent stem cell lines (CMCi006-A and CMCi007-A) from a female and male patient with Fabry disease carrying the same frameshift deletion mutation
Cui S et al. Human-induced pluripotent stem cell lines (CMCi006-A and CMCi007-A) from a female and male patient with Fabry disease carrying the same frameshift deletion mutation. . 2021-03-00. Pubmed ID: 33545641; DOI: 10.1016/j.scr.2021.102214 CMCi006-ACMCi007-A 2021-03-00 2021-03-00 PubMed: 33545641 DOI: 10.1016/j.scr.2021.102214 -
Chen ZT, Zhao ZH, Chen LN, Fan F, Cai GE, Weng HD, Wang YQ, Liao LM, Chen XC, Huang E, Ye QY
Generation of an induced pluripotent stem cell line, FJMUUHi001-A, from a hereditary Parkinson's disease patient with homozygous mutation of c.189dupA in PARK7
Chen ZT et al. Generation of an induced pluripotent stem cell line, FJMUUHi001-A, from a hereditary Parkinson's disease patient with homozygous mutation of c.189dupA in PARK7. . 2021-03-00. Pubmed ID: 33485186; DOI: 10.1016/j.scr.2021.102175 FJMUUHi001-A 2021-03-00 2021-03-00 PubMed: 33485186 DOI: 10.1016/j.scr.2021.102175Associated cell lines:
-
Ko EJ, Cui S, Shin YJ, Lim SW, Lee KI, Lee JY, Yang CW, Kim M, Chung BH
Generation of the human induced pluripotent stem cell lines (CMCi009-A) from a patient with Birt-Hogg-Dubé syndrome (BHD) with heterozygous frameshift deletion mutation c.1285delC of the FLCN gene
Ko EJ et al. Generation of the human induced pluripotent stem cell lines (CMCi009-A) from a patient with Birt-Hogg-Dubé syndrome (BHD) with heterozygous frameshift deletion mutation c.1285delC of the FLCN gene. . 2021-03-00. Pubmed ID: 33540282; DOI: 10.1016/j.scr.2021.102215 CMCi009-A 2021-03-00 2021-03-00 PubMed: 33540282 DOI: 10.1016/j.scr.2021.102215Associated cell lines:
-
Dong W, Shi D, Zhang L, Huang M, Luo Q
Generation of an induced pluripotent stem cell line ZZUNEUi019-A from a five-year-old Chinese girl with Susceptibility to idiopathic generalized epilepsy-15
Dong W et al. Generation of an induced pluripotent stem cell line ZZUNEUi019-A from a five-year-old Chinese girl with Susceptibility to idiopathic generalized epilepsy-15. . 2021-03-00. Pubmed ID: 33540281; DOI: 10.1016/j.scr.2021.102177 SHCDNi001-AZZUNEUi019-A 2021-03-00 2021-03-00 PubMed: 33540281 DOI: 10.1016/j.scr.2021.102177Associated cell lines:
-
Li J, Shang S, Wang T, Fu B, Wang P, Cai G, Chen X, Li Q
Generation of iPSC from peripheral blood mononuclear cells obtained from a patient with TSC2-PKD1 contiguous gene deletion syndrome
Li J et al. Generation of iPSC from peripheral blood mononuclear cells obtained from a patient with TSC2-PKD1 contiguous gene deletion syndrome. . 2021-03-00. Pubmed ID: 33485185; DOI: 10.1016/j.scr.2021.102181 PUMCHi004-A 2021-03-00 2021-03-00 PubMed: 33485185 DOI: 10.1016/j.scr.2021.102181Associated cell lines:
-
Li Y, Liu X, Chen D, Liu Y, Ma Y, Liu Q, Sun W, Li J
Generation of an induced pluripotent stem cell line SDUBMSi005-A from a patient with double primary gastric and colon carcinoma
Li Y et al. Generation of an induced pluripotent stem cell line SDUBMSi005-A from a patient with double primary gastric and colon carcinoma. . 2021-02-27. Pubmed ID: 33770698; DOI: 10.1016/j.scr.2021.102253 SDUBMSi005-A 2021-02-27 2021-02-27 PubMed: 33770698 DOI: 10.1016/j.scr.2021.102253Associated cell lines:
-
Clayton JS, Scriba CK, Romero NB, Malfatti E, Saker S, Larmonier T, Nowak KJ, Ravenscroft G, Laing NG, Taylor RL
Generation of two isogenic induced pluripotent stem cell lines from a 4-month-old severe nemaline myopathy patient with a heterozygous dominant c.553C > A (p.Arg183Ser) variant in the ACTA1 gene
Clayton JS et al. Generation of two isogenic induced pluripotent stem cell lines from a 4-month-old severe nemaline myopathy patient with a heterozygous dominant c.553C > A (p.Arg183Ser) variant in the ACTA1 gene. . 2021-02-26. Pubmed ID: 33740643; DOI: 10.1016/j.scr.2021.102273 HPIi001-AHPIi001-B 2021-02-26 2021-02-26 PubMed: 33740643 DOI: 10.1016/j.scr.2021.102273 -
Wu H, Cheng Y, Lv Z, Liu L, Gong W, Zhang S
Characterization of human induced pluripotent stem cells line JLUEYEi002-A from a 48 year old healthy male
Wu H et al. Characterization of human induced pluripotent stem cells line JLUEYEi002-A from a 48 year old healthy male. . 2021-02-26. Pubmed ID: 33677395; DOI: 10.1016/j.scr.2021.102221 JLUEYEi002-A 2021-02-26 2021-02-26 PubMed: 33677395 DOI: 10.1016/j.scr.2021.102221Associated cell lines:
-
Goh KJ, Tan EK, Lu H, Roy S, Dunn NR
An NKX2-1GFP and TP63tdTomato dual fluorescent reporter for the investigation of human lung basal cell biology
Goh KJ et al. An NKX2-1GFP and TP63tdTomato dual fluorescent reporter for the investigation of human lung basal cell biology. . 2021-02-25. Pubmed ID: 33633173; DOI: 10.1038/s41598-021-83825-6; PMC: PMC7907081 MHHi002-AMHHi006-AMHHi002-A-2MHHi006-A-2MHHi006-A-4 2021-02-25 2021-02-25 PubMed: 33633173 DOI: 10.1038/s41598-021-83825-6Associated cell lines:
-
Appelt PA, Comella K, de Souza LAPS, Luvizutto GJ
Effect of stem cell treatment on functional recovery of spinocerebellar ataxia: systematic review and meta-analysis
Appelt PA et al. Effect of stem cell treatment on functional recovery of spinocerebellar ataxia: systematic review and meta-analysis. . 2021-02-25. Pubmed ID: 33632326; DOI: 10.1186/s40673-021-00130-8; PMC: PMC7905903 CHOPi002-ACHOPi003-A 2021-02-25 2021-02-25 PubMed: 33632326 DOI: 10.1186/s40673-021-00130-8Associated cell lines:
-
Gao X, Qiu SW, Wang WQ, Kang DY, Su N, Dai P, Yuan YY
Generation of a gene corrected human isogenic iPSC line (CPGHi002-A-1) from a DDOD patient with heterozygous c.1516 C>T mutation in the ATP6V1B2 gene
Gao X et al. Generation of a gene corrected human isogenic iPSC line (CPGHi002-A-1) from a DDOD patient with heterozygous c.1516 C>T mutation in the ATP6V1B2 gene. . 2021-02-25. Pubmed ID: 33714068; DOI: 10.1016/j.scr.2021.102271 CPGHi002-ACPGHi002-A-1 2021-02-25 2021-02-25 PubMed: 33714068 DOI: 10.1016/j.scr.2021.102271Associated cell lines:
-
Huang S, Song J, He C, Cai X, Yuan K, Mei L, Feng Y
Genetic insights, disease mechanisms, and biological therapeutics for Waardenburg syndrome
Huang S et al. Genetic insights, disease mechanisms, and biological therapeutics for Waardenburg syndrome. . 2021-02-25. Pubmed ID: 33633356; DOI: 10.1038/s41434-021-00240-2 JTUi002-ATYWHSTi002-AIMAGINi022-A 2021-02-25 2021-02-25 PubMed: 33633356 DOI: 10.1038/s41434-021-00240-2Associated cell lines:
-
Kondrateva E, Demchenko A, Slesarenko Y, Yasinovsky M, Amelina E, Tabakov V, Voronina E, Lavrov A, Smirnikhina S
Derivation of iPSC line (RCMGi002-A) from dermal fibroblasts of a cystic fibrosis female patient with homozygous F508del mutation
Kondrateva E et al. Derivation of iPSC line (RCMGi002-A) from dermal fibroblasts of a cystic fibrosis female patient with homozygous F508del mutation. . 2021-02-25. Pubmed ID: 33684631; DOI: 10.1016/j.scr.2021.102251 RCMGi002-A 2021-02-25 2021-02-25 PubMed: 33684631 DOI: 10.1016/j.scr.2021.102251Associated cell lines:
-
Yde Ohki CM, Grossmann L, Döring C, Hoffmann P, Herms S, Werling AM, Walitza S, Grünblatt E
Generation of integration-free induced pluripotent stem cells from healthy individuals
Yde Ohki CM et al. Generation of integration-free induced pluripotent stem cells from healthy individuals. . 2021-02-24. Pubmed ID: 33667761; DOI: 10.1016/j.scr.2021.102269 TMPi001-ATMPi001-BTMPi002-ATMPi002-BTMPi003-ATMPi003-BTMPi004-ATMPi004-BTMPi005-ATMPi005-B 2021-02-24 2021-02-24 PubMed: 33667761 DOI: 10.1016/j.scr.2021.102269 -
Wang Z, Sun H, Zhang Q, Yang J, Liu Y, Liu H, Shi C, Wang Y, Xu Y
Generation of induced pluripotent stem cell line (ZZUi0024-A) from a 51-year-old patient with APP gene mutation in Alzheimer' s disease
Wang Z et al. Generation of induced pluripotent stem cell line (ZZUi0024-A) from a 51-year-old patient with APP gene mutation in Alzheimer' s disease. . 2021-02-24. Pubmed ID: 33652304; DOI: 10.1016/j.scr.2021.102267 ZZUi024-A 2021-02-24 2021-02-24 PubMed: 33652304 DOI: 10.1016/j.scr.2021.102267Associated cell lines:
-
Grossmann L, Yde Ohki CM, Döring C, Hoffmann P, Herms S, Werling AM, Walitza S, Grünblatt E
Generation of integration-free induced pluripotent stem cell lines from four pediatric ADHD patients
Grossmann L et al. Generation of integration-free induced pluripotent stem cell lines from four pediatric ADHD patients. . 2021-02-24. Pubmed ID: 33662736; DOI: 10.1016/j.scr.2021.102268 TMPi006-ATMPi006-BTMPi007-ATMPi007-BTMPi008-ATMPi009-ATMPi009-B 2021-02-24 2021-02-24 PubMed: 33662736 DOI: 10.1016/j.scr.2021.102268 -
Nikitina TV, Kashevarova AA, Gridina MM, Lopatkina ME, Khabarova AA, Yakovleva YS, Menzorov AG, Minina YA, Pristyazhnyuk IE, Vasilyev SA, Fedotov DA, Serov OL, Lebedev IN
Complex biology of constitutional ring chromosomes structure and (in)stability revealed by somatic cell reprogramming
Nikitina TV et al. Complex biology of constitutional ring chromosomes structure and (in)stability revealed by somatic cell reprogramming. . 2021-02-22. Pubmed ID: 33619287; DOI: 10.1038/s41598-021-83399-3; PMC: PMC7900208 IMGTi001-AIMGTi001-BIMGTi003-AICGi024-AICGi025-A 2021-02-22 2021-02-22 PubMed: 33619287 DOI: 10.1038/s41598-021-83399-3Associated cell lines:
-
Rebs S, Beier J, Argyriou L, Schill T, Hasenfuss G, Vollmann D, Sossalla S, Streckfuss-Bömeke K
Generation and cardiac differentiation of an induced pluripotent stem cell line from a patient with arrhythmia-induced cardiomyopathy
Rebs S et al. Generation and cardiac differentiation of an induced pluripotent stem cell line from a patient with arrhythmia-induced cardiomyopathy. . 2021-02-20. Pubmed ID: 33631417; DOI: 10.1016/j.scr.2021.102263 UMGi157-A 2021-02-20 2021-02-20 PubMed: 33631417 DOI: 10.1016/j.scr.2021.102263Associated cell lines:
-
Janz A, Zink M, Cirnu A, Hartleb A, Albrecht C, Rost S, Klopocki E, Günther K, Edenhofer F, Ergün S, Gerull B
CRISPR/Cas9-edited PKP2 knock-out (JMUi001-A-2) and DSG2 knock-out (JMUi001-A-3) iPSC lines as an isogenic human model system for arrhythmogenic cardiomyopathy (ACM)
Janz A et al. CRISPR/Cas9-edited PKP2 knock-out (JMUi001-A-2) and DSG2 knock-out (JMUi001-A-3) iPSC lines as an isogenic human model system for arrhythmogenic cardiomyopathy (ACM). . 2021-02-18. Pubmed ID: 33640690; DOI: 10.1016/j.scr.2021.102256 JMUi001-AJMUi001-A-2JMUi001-A-3 2021-02-18 2021-02-18 PubMed: 33640690 DOI: 10.1016/j.scr.2021.102256Associated cell lines:
-
Dong L, Zhang H, Quan Y, Jin P, Yang J, Fan X, Fan J, Li M, Gong Y, Wang Y
Establishment and characterization of human induced pluripotent stem cell line (WMUi020-A) from a patient with bicuspid aortic valve aortopathy
Dong L et al. Establishment and characterization of human induced pluripotent stem cell line (WMUi020-A) from a patient with bicuspid aortic valve aortopathy. . 2021-02-18. Pubmed ID: 33631418; DOI: 10.1016/j.scr.2021.102260 WMUi001-AWMUi020-A 2021-02-18 2021-02-18 PubMed: 33631418 DOI: 10.1016/j.scr.2021.102260 -
Wu H, Yang B, Lv Z, Liu L, Gong W, Zhang S
Generation and characterization of human induced pluripotent stem cells line JLUEYEi001-A from a 45 year old female with Stickler syndrome
Wu H et al. Generation and characterization of human induced pluripotent stem cells line JLUEYEi001-A from a 45 year old female with Stickler syndrome. . 2021-02-18. Pubmed ID: 33647874; DOI: 10.1016/j.scr.2021.102255 JLUEYEi001-A 2021-02-18 2021-02-18 PubMed: 33647874 DOI: 10.1016/j.scr.2021.102255Associated cell lines:
-
Marín-Quílez A, García-Tuñón I, Fernández-Infante C, Hernández-Cano L, Palma-Barqueros V, Vuelta E, Sánchez-Martín M, González-Porras JR, Guerrero C, Benito R, Rivera J, Hernández-Rivas JM, Bastida JM
Characterization of the Platelet Phenotype Caused by a Germline RUNX1 Variant in a CRISPR/Cas9-Generated Murine Model
Marín-Quílez A et al. Characterization of the Platelet Phenotype Caused by a Germline RUNX1 Variant in a CRISPR/Cas9-Generated Murine Model. . 2021-02-18. Pubmed ID: 33626581; DOI: 10.1055/s-0041-1723987 GENYOi005-A 2021-02-18 2021-02-18 PubMed: 33626581 DOI: 10.1055/s-0041-1723987Associated cell lines:
-
Guo G, Fu W, Li X, Dong J, Zhao X, Zhang Y
Generation of an iPSC line (ZZUNEUi016-A) derived from a hypertrophic cardiomyopathy patient with the heterozygote mutation in MYH7 gene
Guo G et al. Generation of an iPSC line (ZZUNEUi016-A) derived from a hypertrophic cardiomyopathy patient with the heterozygote mutation in MYH7 gene. . 2021-02-18. Pubmed ID: 33636496; DOI: 10.1016/j.scr.2021.102262 ZZUNEUi016-A 2021-02-18 2021-02-18 PubMed: 33636496 DOI: 10.1016/j.scr.2021.102262Associated cell lines:
-
Ding Y, O'Brien A, Marcó de la Cruz B, Yang M, Lu Y, Qian X, Yang G, McInerney V, Krawczyk J, Lynch SA, Howard L, Allen NM, O'Brien T, Gallagher L, Shen S
Derivation of four iPSC lines from a male ASD patient carrying a deletion in the middle coding region of NRXN1α gene (NUIGi039-A and NUIGi039-B) and a male sibling control (NUIGi040-A and NUIGi040-B)
Ding Y et al. Derivation of four iPSC lines from a male ASD patient carrying a deletion in the middle coding region of NRXN1α gene (NUIGi039-A and NUIGi039-B) and a male sibling control (NUIGi040-A and NUIGi040-B). . 2021-02-18. Pubmed ID: 33631419; DOI: 10.1016/j.scr.2021.102254 NUIGi039-ANUIGi040-ANUIGi039-BNUIGi040-B 2021-02-18 2021-02-18 PubMed: 33631419 DOI: 10.1016/j.scr.2021.102254Associated cell lines:
-
Zhou T, Yang X, Chen Z, Zhou Y, Cao X, Zhao C, Zhao J
A novel COL2A1 mutation causing spondyloepiphyseal dysplasia congenita in a Chinese family
Zhou T et al. A novel COL2A1 mutation causing spondyloepiphyseal dysplasia congenita in a Chinese family. . 2021-02-16. Pubmed ID: 33590889; DOI: 10.1002/jcla.23728 MCRIi001-B 2021-02-16 2021-02-16 PubMed: 33590889 DOI: 10.1002/jcla.23728Associated cell lines:
-
Lima Cunha D, Oram A, Gruber R, Plank R, Lingenhel A, Gupta MK, Altmüller J, Nürnberg P, Schmuth M, Zschocke J, Šarić T, Eckl KM, Hennies HC
hiPSC-Derived Epidermal Keratinocytes from Ichthyosis Patients Show Altered Expression of Cornification Markers
Lima Cunha D et al. hiPSC-Derived Epidermal Keratinocytes from Ichthyosis Patients Show Altered Expression of Cornification Markers. . 2021-02-11. Pubmed ID: 33670118; DOI: 10.3390/ijms22041785; PMC: PMC7916893 UCLi016-AUCLi017-A 2021-02-11 2021-02-11 PubMed: 33670118 DOI: 10.3390/ijms22041785 -
Wang L, Sievert D, Clark AE, Federman H, Gastfriend BD, Shusta E, Palecek SP, Carlin AF, Gleeson J
A Human 3D neural assembloid model for SARS-CoV-2 infection
Wang L et al. A Human 3D neural assembloid model for SARS-CoV-2 infection. . 2021-02-09. Pubmed ID: 33594369; DOI: 10.1101/2021.02.09.430349; PMC: PMC7885921 WAe001-A 2021-02-09 2021-02-09 PubMed: 33594369 DOI: 10.1101/2021.02.09.430349Associated cell lines:
-
Li Q, Sun Y, van IJzendoorn SCD
A Link between Intrahepatic Cholestasis and Genetic Variations in Intracellular Trafficking Regulators
Li Q et al. A Link between Intrahepatic Cholestasis and Genetic Variations in Intracellular Trafficking Regulators. . 2021-02-04. Pubmed ID: 33557414; DOI: 10.3390/biology10020119; PMC: PMC7914782 DHMCi005-A 2021-02-04 2021-02-04 PubMed: 33557414 DOI: 10.3390/biology10020119Associated cell lines:
-
Wißfeld J, Nozaki I, Mathews M, Raschka T, Ebeling C, Hornung V, Brüstle O, Neumann H
Deletion of Alzheimer's disease-associated CD33 results in an inflammatory human microglia phenotype
Wißfeld J et al. Deletion of Alzheimer's disease-associated CD33 results in an inflammatory human microglia phenotype. . 2021-02-04. Pubmed ID: 33539598; DOI: 10.1002/glia.23968 BIONi010-C-5BIONi010-C-9 2021-02-04 2021-02-04 PubMed: 33539598 DOI: 10.1002/glia.23968Associated cell lines:
-
Jansch C, Ziegler GC, Forero A, Gredy S, Wäldchen S, Vitale MR, Svirin E, Zöller JEM, Waider J, Günther K, Edenhofer F, Sauer M, Wischmeyer E, Lesch KP
Serotonin-specific neurons differentiated from human iPSCs form distinct subtypes with synaptic protein assembly
Jansch C et al. Serotonin-specific neurons differentiated from human iPSCs form distinct subtypes with synaptic protein assembly. . 2021-02-00. Pubmed ID: 33560471; DOI: 10.1007/s00702-021-02303-5; PMC: PMC7914246 JMUi001-AUKWMPi001-B 2021-02-00 2021-02-00 PubMed: 33560471 DOI: 10.1007/s00702-021-02303-5Associated cell lines:
-
Zhu K, Ma W, Li J, Zhang YS, Zhang W, Lai H, Wang C
Modeling aortic diseases using induced pluripotent stem cells
Zhu K et al. Modeling aortic diseases using induced pluripotent stem cells. . 2021-02-00. Pubmed ID: 33179450; DOI: 10.1002/sctm.20-0322; PMC: PMC7848399 ISMMSi002-BMHHi012-AMHHi013-AMHHi014-A 2021-02-00 2021-02-00 PubMed: 33179450 DOI: 10.1002/sctm.20-0322Associated cell lines:
-
Sinenko SA, Ponomartsev SV, Tomilin AN
Pluripotent stem cell-based gene therapy approach: human de novo synthesized chromosomes
Sinenko SA et al. Pluripotent stem cell-based gene therapy approach: human de novo synthesized chromosomes. . 2021-02-00. Pubmed ID: 33011821; DOI: 10.1007/s00018-020-03653-1 FAMRCi007-AFAMRCi007-B 2021-02-00 2021-02-00 PubMed: 33011821 DOI: 10.1007/s00018-020-03653-1Associated cell lines:
-
Bose B
Induced Pluripotent Stem Cells (iPSCs) Derived 3D Human Lung Organoids from Different Ethnicities to Understand the SARS-CoV2 Severity/Infectivity Percentage
Bose B. Induced Pluripotent Stem Cells (iPSCs) Derived 3D Human Lung Organoids from Different Ethnicities to Understand the SARS-CoV2 Severity/Infectivity Percentage. . 2021-02-00. Pubmed ID: 32500482; DOI: 10.1007/s12015-020-09989-2; PMC: PMC7272136 CSSi001-A 2021-02-00 2021-02-00 PubMed: 32500482 DOI: 10.1007/s12015-020-09989-2Associated cell lines:
-
Dong Y, Long J, Luo X, Xie G, Xiao ZJ, Tong Y
Targeting of ΔNp63α by miR-522 promotes the migration of breast epithelial cells
Dong Y et al. Targeting of ΔNp63α by miR-522 promotes the migration of breast epithelial cells. . 2021-02-00. Pubmed ID: 33369228; DOI: 10.1002/2211-5463.13072; PMC: PMC7876488 WAe001-AWAe001-A-15 2021-02-00 2021-02-00 PubMed: 33369228 DOI: 10.1002/2211-5463.13072Associated cell lines:
-
Sorriento D, Iaccarino G
The Cardiovascular Phenotype in Fabry Disease: New Findings in the Research Field
Sorriento D et al. The Cardiovascular Phenotype in Fabry Disease: New Findings in the Research Field. . 2021-01-29. Pubmed ID: 33572752; DOI: 10.3390/ijms22031331; PMC: PMC7865937 INSAi002-A 2021-01-29 2021-01-29 PubMed: 33572752 DOI: 10.3390/ijms22031331Associated cell lines:
-
Hey CAB, Larsen LJ, Tümer Z, Brøndum-Nielsen K, Grønskov K, Hjortshøj TD, Møller LB
BBS Proteins Affect Ciliogenesis and Are Essential for Hedgehog Signaling, but Not for Formation of iPSC-Derived RPE-65 Expressing RPE-Like Cells
Hey CAB et al. BBS Proteins Affect Ciliogenesis and Are Essential for Hedgehog Signaling, but Not for Formation of iPSC-Derived RPE-65 Expressing RPE-Like Cells. . 2021-01-29. Pubmed ID: 33572860; DOI: 10.3390/ijms22031345; PMC: PMC7866284 KCi001-AKCi002-A 2021-01-29 2021-01-29 PubMed: 33572860 DOI: 10.3390/ijms22031345 -
Amponsah AE, Guo R, Kong D, Feng B, He J, Zhang W, Liu X, Du X, Ma Z, Liu B, Ma J, Cui H
Patient-derived iPSCs, a reliable in vitro model for the investigation of Alzheimer's disease
Amponsah AE et al. Patient-derived iPSCs, a reliable in vitro model for the investigation of Alzheimer's disease. . 2021-01-29. Pubmed ID: 33550785; DOI: 10.1515/revneuro-2020-0065 HEBHMUi001-A 2021-01-29 2021-01-29 PubMed: 33550785 DOI: 10.1515/revneuro-2020-0065Associated cell lines:
-
Burkert K, Taheri H, Hamad S, Oliverio M, Peinkofer G, Kornfeld JW, Harnying W, Pfannkuche K, Hescheler J, Berkessel A, Šarić T
Salicylic diamines selectively eliminate residual undifferentiated cells from pluripotent stem cell-derived cardiomyocyte preparations
Burkert K et al. Salicylic diamines selectively eliminate residual undifferentiated cells from pluripotent stem cell-derived cardiomyocyte preparations. . 2021-01-27. Pubmed ID: 33504837; DOI: 10.1038/s41598-021-81351-z; PMC: PMC7841182 UKKi007-A 2021-01-27 2021-01-27 PubMed: 33504837 DOI: 10.1038/s41598-021-81351-zAssociated cell lines:
-
Moya-Garzon MD, Gomez-Vidal JA, Alejo-Armijo A, Altarejos J, Rodriguez-Madoz JR, Fernandes MX, Salido E, Salido S, Diaz-Gavilan M
Small Molecule-Based Enzyme Inhibitors in the Treatment of Primary Hyperoxalurias
Moya-Garzon MD et al. Small Molecule-Based Enzyme Inhibitors in the Treatment of Primary Hyperoxalurias. . 2021-01-27. Pubmed ID: 33513899; DOI: 10.3390/jpm11020074; PMC: PMC7912158 CIMAi001-A 2021-01-27 2021-01-27 PubMed: 33513899 DOI: 10.3390/jpm11020074Associated cell lines:
-
Böhnke J, Pinkert S, Schmidt M, Binder H, Bilz NC, Jung M, Reibetanz U, Beling A, Rujescu D, Claus C
Coxsackievirus B3 Infection of Human iPSC Lines and Derived Primary Germ-Layer Cells Regarding Receptor Expression
Böhnke J et al. Coxsackievirus B3 Infection of Human iPSC Lines and Derived Primary Germ-Layer Cells Regarding Receptor Expression. . 2021-01-27. Pubmed ID: 33513663; DOI: 10.3390/ijms22031220; PMC: PMC7865966 WISCi004-ATMOi001-A 2021-01-27 2021-01-27 PubMed: 33513663 DOI: 10.3390/ijms22031220Associated cell lines:
-
Wu F, Chen Y, You K, Tan S, Xu Y, Wang PH, Liu S, Li YX
Generation of WAe001-A-58 human embryonic stem cell line with inducible expression of the SARS-CoV-2 nucleocapsid protein
Wu F et al. Generation of WAe001-A-58 human embryonic stem cell line with inducible expression of the SARS-CoV-2 nucleocapsid protein. . 2021-01-26. Pubmed ID: 33771478; DOI: 10.1016/j.scr.2021.102197; PMC: PMC7835078 WAe001-AWAe001-A-58 2021-01-26 2021-01-26 PubMed: 33771478 DOI: 10.1016/j.scr.2021.102197Associated cell lines:
-
Alonso-Barroso E, Pérez B, Desviat LR, Richard E
Cardiomyocytes Derived from Induced Pluripotent Stem Cells as a Disease Model for Propionic Acidemia
Alonso-Barroso E et al. Cardiomyocytes Derived from Induced Pluripotent Stem Cells as a Disease Model for Propionic Acidemia. . 2021-01-25. Pubmed ID: 33503868; DOI: 10.3390/ijms22031161; PMC: PMC7865492 UAMi001-A 2021-01-25 2021-01-25 PubMed: 33503868 DOI: 10.3390/ijms22031161Associated cell lines:
-
Wu S.
Research progress in differentiation of male germ cells derived from induced pluripotent stem cells in vitro
Wu S.. Research progress in differentiation of male germ cells derived from induced pluripotent stem cells in vitro. . 2021-01-25. DOI: 10.3760/cma.j.cn101441-20200111-00021 HUSTi001-A 2021-01-25 2021-01-25 DOI: 10.3760/cma.j.cn101441-20200111-00021Associated cell lines:
-
Ronchi C, Bernardi J, Mura M, Stefanello M, Badone B, Rocchetti M, Crotti L, Brink P, Schwartz PJ, Gnecchi M, Zaza A
NOS1AP polymorphisms reduce NOS1 activity and interact with prolonged repolarization in arrhythmogenesis
Ronchi C et al. NOS1AP polymorphisms reduce NOS1 activity and interact with prolonged repolarization in arrhythmogenesis. . 2021-01-21. Pubmed ID: 32061134; DOI: 10.1093/cvr/cvaa036; PMC: PMC7820868 PSMi007-A 2021-01-21 2021-01-21 PubMed: 32061134 DOI: 10.1093/cvr/cvaa036Associated cell lines:
-
Elsayed AK, Younis I, Ali G, Hussain K, Abdelalim EM
Aberrant development of pancreatic beta cells derived from human iPSCs with FOXA2 deficiency
Elsayed AK et al. Aberrant development of pancreatic beta cells derived from human iPSCs with FOXA2 deficiency. . 2021-01-20. Pubmed ID: 33473118; DOI: 10.1038/s41419-021-03390-8; PMC: PMC7817686 QBRIi009-A 2021-01-20 2021-01-20 PubMed: 33473118 DOI: 10.1038/s41419-021-03390-8Associated cell lines:
-
Manini A, Pantoni L
CADASIL from Bench to Bedside: Disease Models and Novel Therapeutic Approaches
Manini A et al. CADASIL from Bench to Bedside: Disease Models and Novel Therapeutic Approaches. . 2021-01-19. Pubmed ID: 33464533; DOI: 10.1007/s12035-021-02282-4 IDISi001-A 2021-01-19 2021-01-19 PubMed: 33464533 DOI: 10.1007/s12035-021-02282-4Associated cell lines:
-
Kulikova O, Brodehl A, Kiseleva A, Myasnikov R, Meshkov A, Stanasiuk C, Gärtner A, Divashuk M, Sotnikova E, Koretskiy S, Kharlap M, Kozlova V, Mershina E, Pilus P, Sinitsyn V, Milting H, Boytsov S, Drapkina O
The Desmin (DES) Mutation p.A337P Is Associated with Left-Ventricular Non-Compaction Cardiomyopathy
Kulikova O et al. The Desmin (DES) Mutation p.A337P Is Associated with Left-Ventricular Non-Compaction Cardiomyopathy. . 2021-01-19. Pubmed ID: 33478057; DOI: 10.3390/genes12010121; PMC: PMC7835827 UKKi011-A 2021-01-19 2021-01-19 PubMed: 33478057 DOI: 10.3390/genes12010121Associated cell lines:
-
Lau S, Gossen M, Lendlein A, Jung F
Venous and Arterial Endothelial Cells from Human Umbilical Cords: Potential Cell Sources for Cardiovascular Research
Lau S et al. Venous and Arterial Endothelial Cells from Human Umbilical Cords: Potential Cell Sources for Cardiovascular Research. . 2021-01-19. Pubmed ID: 33478148; DOI: 10.3390/ijms22020978; PMC: PMC7835953 IHSTMi001-A 2021-01-19 2021-01-19 PubMed: 33478148 DOI: 10.3390/ijms22020978Associated cell lines:
-
García-López M, Arenas J, Gallardo ME
Hereditary Optic Neuropathies: Induced Pluripotent Stem Cell-Based 2D/3D Approaches
García-López M et al. Hereditary Optic Neuropathies: Induced Pluripotent Stem Cell-Based 2D/3D Approaches. . 2021-01-18. Pubmed ID: 33477675; DOI: 10.3390/genes12010112; PMC: PMC7831942 IISHDOi003-AFINCBi001-AIISHDOi006-A 2021-01-18 2021-01-18 PubMed: 33477675 DOI: 10.3390/genes12010112Associated cell lines:
-
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:
-
Arber C, Lovejoy C, Harris L, Willumsen N, Alatza A, Casey JM, Lines G, Kerins C, Mueller AK, Zetterberg H, Hardy J, Ryan NS, Fox NC, Lashley T, Wray S
Familial Alzheimer's Disease Mutations in PSEN1 Lead to Premature Human Stem Cell Neurogenesis
Arber C et al. Familial Alzheimer's Disease Mutations in PSEN1 Lead to Premature Human Stem Cell Neurogenesis. . 2021-01-12. Pubmed ID: 33440141; DOI: 10.1016/j.celrep.2020.108615; PMC: PMC7809623 RBi001-A 2021-01-12 2021-01-12 PubMed: 33440141 DOI: 10.1016/j.celrep.2020.108615Associated cell lines:
-
Völkner C, Liedtke M, Hermann A, Frech MJ
Pluripotent Stem Cells for Disease Modeling and Drug Discovery in Niemann-Pick Type C1
Völkner C et al. Pluripotent Stem Cells for Disease Modeling and Drug Discovery in Niemann-Pick Type C1. . 2021-01-12. Pubmed ID: 33445799; DOI: 10.3390/ijms22020710; PMC: PMC7828283 AKOSi001-ATRNDi001-DAKOSi004-AAKOSi005-AAKOSi006-AAKOSi007-A 2021-01-12 2021-01-12 PubMed: 33445799 DOI: 10.3390/ijms22020710Associated cell lines:
-
Nilsson F, Storm P, Sozzi E, Hidalgo Gil D, Birtele M, Sharma Y, Parmar M, Fiorenzano A
Single-Cell Profiling of Coding and Noncoding Genes in Human Dopamine Neuron Differentiation
Nilsson F et al. Single-Cell Profiling of Coding and Noncoding Genes in Human Dopamine Neuron Differentiation. . 2021-01-12. Pubmed ID: 33445654; DOI: 10.3390/cells10010137; PMC: PMC7827700 RCe021-A 2021-01-12 2021-01-12 PubMed: 33445654 DOI: 10.3390/cells10010137Associated cell lines:
-
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:
-
Reinert LS, Rashidi AS, Tran DN, Katzilieris-Petras G, Hvidt AK, Gohr M, Fruhwürth S, Bodda C, Thomsen MK, Vendelbo MH, Khan AR, Hansen B, Bergström P, Agholme L, Mogensen TH, Christensen MH, Nyengaard JR, Sen GC, Zetterberg H, Verjans GM, Paludan SR
Brain immune cells undergo cGAS/STING-dependent apoptosis during herpes simplex virus type 1 infection to limit type I IFN production
Reinert LS et al. Brain immune cells undergo cGAS/STING-dependent apoptosis during herpes simplex virus type 1 infection to limit type I IFN production. . 2021-01-04. Pubmed ID: 32990676; DOI: 10.1172/jci136824; PMC: PMC7773356 WTSIi015-A 2021-01-04 2021-01-04 PubMed: 32990676 DOI: 10.1172/jci136824Associated cell lines:
-
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:
-
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:
-
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:
-
Fiorenzano A, Birtele M, Wahlestedt J, Parmar M.
Evaluation of TH-Cre knock-in cell lines for detection and specific targeting of stem cell-derived dopaminergic neurons
Fiorenzano A et al. Evaluation of TH-Cre knock-in cell lines for detection and specific targeting of stem cell-derived dopaminergic neurons. . 2021-01-01. RCe021-A 2021-01-01 2021-01-01Associated cell lines:
-
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:
-
Zhang X, Ding J, Xia S
A preliminary study of MMP-9 and sCD40L in patients with coronary slow flow
Zhang X et al. A preliminary study of MMP-9 and sCD40L in patients with coronary slow flow. . 2021-01-00. Pubmed ID: 33545794; DOI: 10.21037/apm-20-2271 SYSUi002-A 2021-01-00 2021-01-00 PubMed: 33545794 DOI: 10.21037/apm-20-2271Associated cell lines:
-
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:
-
Fiorenzano A, Birtele M, Wahlestedt JN, Parmar M
Evaluation of TH-Cre knock-in cell lines for detection and specific targeting of stem cell-derived dopaminergic neurons
Fiorenzano A et al. Evaluation of TH-Cre knock-in cell lines for detection and specific targeting of stem cell-derived dopaminergic neurons. . 2021-01-00. Pubmed ID: 33532642; DOI: 10.1016/j.heliyon.2021.e06006; PMC: PMC7821040 RCe021-A 2021-01-00 2021-01-00 PubMed: 33532642 DOI: 10.1016/j.heliyon.2021.e06006Associated cell lines:
-
Fang Jing, Wang Yanlin, Wang Zhuoya, Sun Huifang, Zhang Qi, Yang Jing, Liu Yutao, Liu Han, Shi Changhe, Kan Quancheng, Xu Yuming
Generation of induced pluripotent stem cell line (ZZUi0026-A) from a patient with spinocerebellar ataxia type 3
Fang Jing et al. Generation of induced pluripotent stem cell line (ZZUi0026-A) from a patient with spinocerebellar ataxia type 3. . 2021-01-00. DOI: 10.1016/j.scr.2021.102205 ZZUi026-A 2021-01-00 2021-01-00 DOI: 10.1016/j.scr.2021.102205Associated cell lines:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
Wang L, Li X, Fu W, Zhang S, Du W, Zhao J, Liu M, Wang M, Liu Y, Hu L, Ding Z, Li L, Zhao X, Dong J
Generation of an IPSC line from a patient with hypertrophic cardiomyopathy carrying a mutation in MYH6 gene
Wang L et al. Generation of an IPSC line from a patient with hypertrophic cardiomyopathy carrying a mutation in MYH6 gene. . 2020-12-24. Pubmed ID: 33385793; DOI: 10.1016/j.scr.2020.102138 ZZUNEUi013-A 2020-12-24 2020-12-24 PubMed: 33385793 DOI: 10.1016/j.scr.2020.102138Associated cell lines:
-
Toledo MAS, Gatz M, Sontag S, Gleixner KV, Eisenwort G, Feldberg K, Hamouda AEI, Kluge F, Guareschi R, Rossetti G, Sechi AS, Dufva O, Mustjoki S, Maurer A, Schüler HM, Goetzke R, Braunschweig T, Kaiser A, Panse JP, Jawhar M, Reiter A, Hilberg F, Ettmayer P, Wagner W, Koschmieder S, Brümmendorf TH, Valent P, Chatain N, Zenke M
Nintedanib Targets KIT D816V Neoplastic Cells Derived from Induced Pluripotent Stem cells of Systemic Mastocytosis
Toledo MAS et al. Nintedanib Targets KIT D816V Neoplastic Cells Derived from Induced Pluripotent Stem cells of Systemic Mastocytosis. . 2020-12-23. Pubmed ID: 33512435; DOI: 10.1182/blood.2019004509 UKAi004-AUKAi004-BUKAi004-CUKAi004-DUKAi004-EUKAi007-AUKAi007-BUKAi008-AUKAi008-BUKAi008-CESIBIe003-A-8ESIBIe003-A-9 2020-12-23 2020-12-23 PubMed: 33512435 DOI: 10.1182/blood.2019004509 -
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:
-
Cheng YS, Yang S, Hong J, Li R, Beers J, Zou J, Huang W, Zheng W
Modeling CNS Involvement in Pompe Disease Using Neural Stem Cells Generated from Patient-Derived Induced Pluripotent Stem Cells
Cheng YS et al. Modeling CNS Involvement in Pompe Disease Using Neural Stem Cells Generated from Patient-Derived Induced Pluripotent Stem Cells. . 2020-12-22. Pubmed ID: 33375166; DOI: 10.3390/cells10010008; PMC: PMC7822217 TRNDi007-B 2020-12-22 2020-12-22 PubMed: 33375166 DOI: 10.3390/cells10010008Associated cell lines:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
Fiacco E, Alowaysi M, Astro V, Adamo A
Generation of an iPSC cohort of isogenic iPSC lines (46-XY and 47-XXY) from a non-mosaic Klinefelter Syndrome patient (47-XXY) (KAUSTi008-A, KAUSTi008-B, KAUSTi008-C, KAUSTi008-D, KAUSTi008-E, KAUSTi008-F, KAUSTi008-G)
Fiacco E et al. Generation of an iPSC cohort of isogenic iPSC lines (46-XY and 47-XXY) from a non-mosaic Klinefelter Syndrome patient (47-XXY) (KAUSTi008-A, KAUSTi008-B, KAUSTi008-C, KAUSTi008-D, KAUSTi008-E, KAUSTi008-F, KAUSTi008-G). . 2020-12-10. Pubmed ID: 33333453; DOI: 10.1016/j.scr.2020.102119 KAUSTi003-AKAUSTi004-AKAUSTi004-BKAUSTi005-AKAUSTi005-BKAUSTi005-CKAUSTi006-AKAUSTi006-BKAUSTi008-AKAUSTi008-BKAUSTi008-CKAUSTi008-DKAUSTi008-EKAUSTi008-FKAUSTi008-GKAUSTi008-F-1KAUSTi008-F-2 2020-12-10 2020-12-10 PubMed: 33333453 DOI: 10.1016/j.scr.2020.102119 -
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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 -
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:
-
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:
-
Nishihara H, Gastfriend BD, Soldati S, Perriot S, Mathias A, Sano Y, Shimizu F, Gosselet F, Kanda T, Palecek SP, Du Pasquier R, Shusta EV, Engelhardt B
Advancing human induced pluripotent stem cell-derived blood-brain barrier models for studying immune cell interactions
Nishihara H et al. Advancing human induced pluripotent stem cell-derived blood-brain barrier models for studying immune cell interactions. . 2020-12-00. Pubmed ID: 33124083; DOI: 10.1096/fj.202001507rr; PMC: PMC7686106 CHUVi001-A 2020-12-00 2020-12-00 PubMed: 33124083 DOI: 10.1096/fj.202001507rrAssociated cell lines:
-
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:
-
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:
-
Wang Z, Cui Y, Shan Y, Kang B, Shi L, Geng K, Han J
Generation of a MCPH1 knockout human embryonic stem cell line by CRISPR/Cas9 technology
Wang Z et al. Generation of a MCPH1 knockout human embryonic stem cell line by CRISPR/Cas9 technology. . 2020-12-00. Pubmed ID: 33370873; DOI: 10.1016/j.scr.2020.102105 WAe001-A-52 2020-12-00 2020-12-00 PubMed: 33370873 DOI: 10.1016/j.scr.2020.102105Associated cell lines:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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 -
Santos Hallana Souza, Poletto Edina, Schuh Roselena, Matte Ursula, Baldo Guilherme
Genome editing in mucopolysaccharidoses and mucolipidoses
Santos Hallana Souza et al. Genome editing in mucopolysaccharidoses and mucolipidoses. . 2021-00-00. DOI: 10.1016/bs.pmbts.2021.01.026 TRNDi005-ABRCi001-ATRNDi006-A 2021-00-00 2021-00-00 DOI: 10.1016/bs.pmbts.2021.01.026Associated cell lines:
-
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:
-
Ji X, Tang Q, Tang C, Wu Z, Ma L, Guo X, Cheng G, Chen Y, Yang T, Xiong M, Zhou W
Generation of an induced pluripotent stem cell line from an Alström Syndrome patient with ALMS1 mutation (c.3902C > A, c.6436C > T) and a gene correction isogenic iPSC line
Ji X et al. Generation of an induced pluripotent stem cell line from an Alström Syndrome patient with ALMS1 mutation (c.3902C > A, c.6436C > T) and a gene correction isogenic iPSC line. . 2020-12-00. Pubmed ID: 33264725; DOI: 10.1016/j.scr.2020.102089 FDCHi003-AFDCHi003-A-1 2020-12-00 2020-12-00 PubMed: 33264725 DOI: 10.1016/j.scr.2020.102089Associated cell lines:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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 -
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:
-
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:
-
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:
-
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:
-
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:
-
Schäfer-Korting M, Zoschke C
How Qualification of 3D Disease Models Cuts the Gordian Knot in Preclinical Drug Development
Schäfer-Korting M et al. How Qualification of 3D Disease Models Cuts the Gordian Knot in Preclinical Drug Development. . 2021-00-00. Pubmed ID: 32894342; DOI: 10.1007/164_2020_374 KCLi001-A 2021-00-00 2021-00-00 PubMed: 32894342 DOI: 10.1007/164_2020_374Associated cell lines:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
Hsia GSP, Esposito J, da Rocha LA, Ramos SLG, Okamoto OK
Clinical Application of Human Induced Pluripotent Stem Cell-Derived Organoids as an Alternative to Organ Transplantation
Hsia GSP et al. Clinical Application of Human Induced Pluripotent Stem Cell-Derived Organoids as an Alternative to Organ Transplantation. . 2021-00-00. Pubmed ID: 33679987; DOI: 10.1155/2021/6632160; PMC: PMC7929656 WAe009-A 2021-00-00 2021-00-00 PubMed: 33679987 DOI: 10.1155/2021/6632160Associated cell lines:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
Li J, Li Y, Zhan XY, Ran X, Tse HF, Dang S, Nie Y, Huang K
Generation of GADD45A gene knockout human embryonic stem cell line using CRISPR/Cas9
Li J et al. Generation of GADD45A gene knockout human embryonic stem cell line using CRISPR/Cas9. . 2020-12-00. Pubmed ID: 33232900; DOI: 10.1016/j.scr.2020.102090 WAe001-A-59 2020-12-00 2020-12-00 PubMed: 33232900 DOI: 10.1016/j.scr.2020.102090Associated cell lines:
-
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:
-
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:
-
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:
-
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:
-
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 -
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:
-
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:
-
Shaker MR, Pietrogrande G, Martin S, Lee JH, Sun W, Wolvetang EJ
Rapid and Efficient Generation of Myelinating Human Oligodendrocytes in Organoids
Shaker MR et al. Rapid and Efficient Generation of Myelinating Human Oligodendrocytes in Organoids. . 2021-00-00. Pubmed ID: 33815061; DOI: 10.3389/fncel.2021.631548; PMC: PMC8010307 UCSFi001-A 2021-00-00 2021-00-00 PubMed: 33815061 DOI: 10.3389/fncel.2021.631548Associated cell lines:
-
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:
-
Yan R, Liu P, Li F, Chu M, Lei J, Wang F, Luo L, Xu X
Generation of a human induced pluripotent stem cell line (SBWCHi001-A) from a patient with NEDSDV carrying a pathogenic mutation in CTNNB1 gene
Yan R et al. Generation of a human induced pluripotent stem cell line (SBWCHi001-A) from a patient with NEDSDV carrying a pathogenic mutation in CTNNB1 gene. . 2020-12-00. Pubmed ID: 33264726; DOI: 10.1016/j.scr.2020.102091 SBWCHi001-A 2020-12-00 2020-12-00 PubMed: 33264726 DOI: 10.1016/j.scr.2020.102091Associated cell lines:
-
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:
-
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:
-
Sar Pranati, Dalai Sarat
CRISPR/Cas9 in epigenetics studies of health and disease
Sar Pranati et al. CRISPR/Cas9 in epigenetics studies of health and disease. . 2021-00-00. DOI: 10.1016/bs.pmbts.2021.01.022 CSSi002-A 2021-00-00 2021-00-00 DOI: 10.1016/bs.pmbts.2021.01.022Associated cell lines:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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 -
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:
-
Ahmed Engi, Fieldes Mathieu, Bourguignon Chloé, Mianné Joffrey, Petit Aurélie, Vernisse Charlotte, Jory Myriam, Cazevieille Chantal, Boukhaddaoui Hassan, Garnett James P., Massiera Gladys, Vachier Isabelle, Assou Said, Bourdin Arnaud, De Vos John
Differentiation of human induced pluripotent stem cells into functional airway epithelium
Ahmed Engi et al. Differentiation of human induced pluripotent stem cells into functional airway epithelium. . 2020-11-29. DOI: 10.1101/2020.11.29.400358 UHOMi001-AUHOMi002-AUHOMi003-AUHOMi004-AUHOMi005-A 2020-11-29 2020-11-29 DOI: 10.1101/2020.11.29.400358Associated cell lines:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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 -
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:
-
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 -
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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 -
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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 -
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:
-
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:
-
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:
-
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:
-
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 -
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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 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 -
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:
-
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:
-
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:
-
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:
-
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:
-
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 -
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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 -
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 -
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 -
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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 -
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:
-
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 -
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:
-
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:
-
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:
-
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:
-
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 -
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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 -
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 -
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:
-
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 -
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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 -
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:
-
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:
-
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:
-
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:
-
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 -
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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:
-
Chen D, Li Z, Liu Y, Sampaio N, Yang D, Aksentijevich I, Boehm M, Chen G
Human induced pluripotent stem cells generated from a patient with a homozygous L272P mutation in the OTULIN gene (NIHTVBi014-A)
Chen D et al. Human induced pluripotent stem cells generated from a patient with a homozygous L272P mutation in the OTULIN gene (NIHTVBi014-A). . 2020-07-20. Pubmed ID: 32721894; DOI: 10.1016/j.scr.2020.101921; PMC: PMC7855794 NIHTVBi014-A 2020-07-20 2020-07-20 PubMed: 32721894 DOI: 10.1016/j.scr.2020.101921Associated cell lines:
-
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:
-
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:
-
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:
-
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:
-
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:
-
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-thalassaem