诱导多能干细胞
生物
色素性视网膜炎
重编程
复合杂合度
突变
遗传学
干细胞
分子生物学
表型
视网膜变性
癌症研究
胚胎干细胞
细胞
基因
作者
Yalan Zhou,Chengcheng Ding,Shu‐Tao Xia,Yutong Jing,Shengru Mao,Jian Liu,Juan Chen,Hon Fai Chan,Shibo Tang,Jiansu Chen
标识
DOI:10.1016/j.scr.2020.101742
摘要
Crumbs homologue 1 (CRB1) mutations have been found in retinitis pigmentosa (RP) patients lead to severe retinal dystrophies. The human induced pluripotent stem (iPS) cell line CSUASOi003-A derived from peripheral blood mononuclear cells (PBMCs) of a patient carrying two heterozygous mutations (2249G>A p.G750D and c.2809G>A p.A937T) in CRB1 gene was generated by non-integrative reprogramming technology. Pluripotency and differentiation capacity were assessed by immunocytochemistry and quantitative polymerase chain reaction (qPCR). The RP patient-specific iPS cell line provide a powerful model for evaluating the pathological phenotypes of the disease.
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