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- immunocytochemistry; human; 1:100; loading ...; fig s1g
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- immunohistochemistry - frozen section; chicken; 1:1000; fig 5m
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| Adhicary S, Ye S, Lin H, Texter K, Garg V, Zhao M. Establishment of NCHi009-A, an iPSC line from a patient with hypoplastic left heart syndrome (HLHS) carrying a heterozygous NOTCH1 mutation. Stem Cell Res. 2023;66:103013 pubmed publisher
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| Li L, Si X, Yang J, Lei M, Liu H, Ruan J, et al. Generation of a human iPSC line (CIBi014-A) from a patient with Parkinson's disease carrying a novel heterozygotic PARK8 (LRRK2) mutation. Stem Cell Res. 2023;66:102995 pubmed publisher
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| Chen I, Olshausen J, Thomas D, Lai C, McLaughlin T, Wu J. Generation of three induced pluripotent stem cell lines to model and investigate diseases affecting Hispanics. Stem Cell Res. 2022;65:102969 pubmed publisher
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| Contreras J, Alonzo M, Ye S, Lin H, Hernandez Rosario L, McBride K, et al. Generation of an induced pluripotent stem cell line NCHi003-A from a 11-year-old male with pulmonary atresia with intact ventricular septum (PA-IVS). Stem Cell Res. 2022;64:102893 pubmed publisher
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| Jiang Z, Gu X, Su W, Duan Q, Lin J, Cao B, et al. Production of a human iPSC line from an early-onset Parkinson's disease patient with a novel CHCHD2 gene truncated mutation. Stem Cell Res. 2022;64:102881 pubmed publisher
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| Liu J, Black G, Kimber S, Sergouniotis P. Generation of a human induced pluripotent stem cell line carrying the TYR c.575C>A (p.Ser192Tyr) and c.1205G>A (p.Arg402Gln) variants in homozygous state using CRISPR-Cas9 genome editing. Stem Cell Res. 2022;64:102880 pubmed publisher
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| Chen Y, Huang P, Wen M, Pan M, Lee D, Chen T. Generation of a homozygous knock-in human embryonic stem cell line expressing mEos4b-tagged CTR1. Stem Cell Res. 2022;63:102845 pubmed publisher
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| B xe9 renger Currias N, Mircea M, Adegeest E, van den Berg P, Feliksik M, Hochane M, et al. A gastruloid model of the interaction between embryonic and extra-embryonic cell types. J Tissue Eng. 2022;13:20417314221103042 pubmed publisher
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| Shi Y, Wu S, Yang B, Yu B, Yan Y, Yang J, et al. Generation of a human iPSC line CIBi011-A from amniocytes of a healthy fetus. Stem Cell Res. 2022;62:102801 pubmed publisher
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| Fan Y, Zhao L, Lai Y, Lu K, Huang J. CRISPR-Cas9-mediated loss of function of β-catenin attenuates intervertebral disc degeneration. Mol Ther Nucleic Acids. 2022;28:387-396 pubmed publisher
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| Lee H, Kim A, Hwang S, Jung J, Seol H, Sung J, et al. Generation of αMHC-EGFP knock-in in human pluripotent stem cell line, SNUe003-A-3 using CRISPR/Cas9-based gene targeting. Stem Cell Res. 2022;61:102779 pubmed publisher
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| Hu X, Xiong S, Zhou X, Sun L. Generation of a human induced pluripotent stem cell line FMUPDCi001-A from a patient with mental retardation, autosomal recessive 36 (MRT36) carrying the variants c.219dupA and c.587C > T in ADAT3. Stem Cell Res. 2022;61:102777 pubmed publisher
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| Breyer M, Klein T, Klug K, Klopocki E, Uceyler N. Generation of the induced pluripotent stem cell line UKWNLi005-A derived from a patient with the GLA mutation c.376A > G of unknown pathogenicity in Fabry disease. Stem Cell Res. 2022;61:102747 pubmed publisher
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| Belbachir N, Lai C, Rhee J, Zhuge Y, PEREZ M, Sallam K, et al. Generation of two induced pluripotent stem cell lines from Brugada syndrome affected patients carrying SCN5A mutations. Stem Cell Res. 2021;57:102605 pubmed publisher
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| Shamshirgaran Y, Jonebring A, Svensson A, Leefa I, Bohlooly Y M, Firth M, et al. Rapid target validation in a Cas9-inducible hiPSC derived kidney model. Sci Rep. 2021;11:16532 pubmed publisher
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| Iannello G, Patel A, Sirabella D, Corneo B, Thaker V. Generation of the iPSC line CUIMCi003-A derived from a patient with severe early onset obesity. Stem Cell Res. 2021;54:102432 pubmed publisher
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| Ma L, Schmidt M, Morrow E. Human iPSC lines from a Christianson syndrome patient with NHE6 W523X mutation, a biologically-related control, and CRISPR/Cas9 gene-corrected isogenic controls. Stem Cell Res. 2021;54:102435 pubmed publisher
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| Argenziano M, Burgos Angulo M, Najari Beidokhti M, Yang J, Bertalovitz A, McDonald T. Generation of a heterozygous FLNC mutation-carrying human iPSC line, USFi002-A, for modeling dilated cardiomyopathy. Stem Cell Res. 2021;53:102394 pubmed publisher
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| Beylina A, Langston R, Rosen D, Reed X, Cookson M. Generation of fourteen isogenic cell lines for Parkinson's disease-associated leucine-rich repeat kinase (LRRK2). Stem Cell Res. 2021;53:102354 pubmed publisher
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| Yang J, Samal E, Burgos Angulo M, Bertalovitz A, McDonald T. Establishment of an arrhythmogenic right ventricular cardiomyopathy derived iPSC cell line (USFi004-A) carrying a heterozygous mutation in PKP2 (c.1799delA). Stem Cell Res. 2021;54:102398 pubmed publisher
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| Yang J, Burgos Angulo M, Argenziano M, Bertalovitz A, Najari Beidokhti M, McDonald T. Generation of an iPSC cell line (USFi003-A) from a patient with dilated cardiomyopathy carrying a heterozygous mutation in LMNA (p.R541C). Stem Cell Res. 2021;54:102396 pubmed publisher
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| Morgani S, Su J, Nichols J, Massague J, Hadjantonakis A. The transcription factor Rreb1 regulates epithelial architecture, invasiveness, and vasculogenesis in early mouse embryos. elife. 2021;10: pubmed publisher
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| Lucchino V, Scaramuzzino L, Scalise S, Grillone K, Lo Conte M, Esposito C, et al. Generation of human induced pluripotent stem cell lines (UNIMGi003-A and UNIMGi004-A) from two Italian siblings affected by Unverricht-Lundborg disease. Stem Cell Res. 2021;53:102329 pubmed publisher
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| Ma L, Prada A, Schmidt M, Morrow E. Generation of pathogenic TPP1 mutations in human stem cells as a model for neuronal ceroid lipofuscinosis type 2 disease. Stem Cell Res. 2021;53:102323 pubmed publisher
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| Devito L, 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. Stem Cell Res. 2021;53:102304 pubmed publisher
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| Liu L, Shenoy S, Jahng J, Liu Y, Knowles J, Zhuge Y, et al. Generation of two heterozygous MYBPC3 mutation-carrying human iPSC lines, SCVIi001-A and SCVIi002-A, for modeling hypertrophic cardiomyopathy. Stem Cell Res. 2021;53:102279 pubmed publisher
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