生物
诱导多能干细胞
重编程
SOX2
KLF4公司
色素性视网膜炎
突变
外周血单个核细胞
遗传学
基因
癌症研究
分子生物学
胚胎干细胞
体外
作者
Yan-Ping Li,Hui Liu,Zi‐Bing Jin
标识
DOI:10.1016/j.scr.2020.102075
摘要
Mutation in SLC7A14 gene causes autosomal recessive retinitis pigmentosa (arRP). Here we describe the generation and characterization of human induced pluripotent stem cell (hiPSC) lines of RP patient with SLC7A14 mutation and his healthy parents. hiPSCs were derived from peripheral blood mononuclear cells (PBMCs) reprogrammed with integration-free plasmids including the reprogramming factors OCT3/4, SOX2, MYC and KLF4. All the established hiPSC lines showed normal karyotype, pluripotency and differentiation capacity.
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