生物
诱导多能干细胞
SOX2
重编程
杂合子优势
复合杂合度
KLF4公司
枫糖尿病
胚芽层
分子生物学
外周血单个核细胞
核型
基因
杂合子丢失
突变
遗传学
体外
癌症研究
基因型
染色体
等位基因
转录因子
氨基酸
胚胎干细胞
亮氨酸
作者
Haiyan Zhang,Yanyan Ma,Xiaomei Li,Xiaomeng Yang,Yue Li,Jingyun Guan,Rui Dong,Zhongtao Gai,Yi Liu
标识
DOI:10.1016/j.scr.2019.101585
摘要
The human induced pluripotent stem cell (iPSC) line SDQLCHi013-A was generated from peripheral blood mononuclear cells of a 7-day-old infant, who was diagnosed with maple syrup urine disease and carried compound heterozygote mutations (c.1280_1282 delTGG and c.632C>T) in BCKDHA gene. Non-integrating episomal vectors coding OCT4, SOX2, KLF4, BCL-XL and MYC were used for reprogramming. The established iPSC line contained the same mutations found in the patient, possessed a normal karyotype, could differentiate into cells of three germ layers in vitro and expressed pluripotency markers.
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