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首页> 外文期刊>Stem cell research >Generation of a human iPSC line from a patient with retinitis pigmentosa caused by mutation in PRPF8 gene - ScienceDirect
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Generation of a human iPSC line from a patient with retinitis pigmentosa caused by mutation in PRPF8 gene - ScienceDirect

机译:由PRPF8基因突变引起的色素性视网膜炎患者生成人iPSC细胞系-ScienceDirect

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摘要

The human iPSC cell line, RP2-FiPS4F1 (RCPFi001-A), derived from dermal fibroblasts from the patient with retinitis pigmentosa caused by the mutation of the gene PRPF8, was generated by non-integrative reprogramming technology using OCT3/4, SOX2, CMYC and KLF4 reprogramming factors.
机译:通过使用OCT3 / 4,SOX2,CMYC的非整合重编程技术产生了人iPSC细胞系RP2-FiPS4F1(RCPFi001-A),该细胞系来源于色素PREF8基因突变引起的色素性视网膜炎患者的皮肤成纤维细胞和KLF4重编程因子。

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