当前位置: X-MOL 学术Stem Cell Res. › 论文详情
Our official English website, www.x-mol.net, welcomes your feedback! (Note: you will need to create a separate account there.)
Generation of an integration-free induced pluripotent stem cell (iPSC) line (ZZUNEUi005-A) from a Wilson's disease patient harboring a homozygous Pro992Leu mutation in ATP7B gene.
Stem Cell Research ( IF 1.2 ) Pub Date : 2020-07-15 , DOI: 10.1016/j.scr.2020.101909
Liting Wei 1 , Jiwei Zhang 2 , Dingbang Chen 3 , Li Feng 3 , Chao Wu 3 , Rui Wang 4 , Xunhua Li 3
Affiliation  

Using non-integrative reprogramming method, a human induced pluripotent stem cell (iPSC) line, ZZUNEUi005-A, was generated from a 36-year-old male patient with Wilson’s disease, carrying a homozygous Pro992Leu mutation in the ATP7B gene. This cell line shows pluripotency both in vitro and in vivo and has a normal karyotype. Furthermore, we showed that this iPSC line could be differentiated into neural and hepatocyte-like cells.



中文翻译:

从具有ATP7B基因纯合Pro992Leu突变的威尔逊病患者中产生无整合诱导多能干细胞(iPSC)系(ZZUNEUi005-A)。

使用非整合重编程方法,从一名威尔逊氏病的36岁男性患者中产生了人类诱导的多能干细胞(iPSC)系ZZUNEUi005-A,该患者在ATP7B基因中携带纯合Pro992Leu突变。该细胞系在体外和体内均显示多能性,并具有正常的核型。此外,我们表明,该iPSC系可以分化为神经细胞和肝细胞样细胞。

更新日期:2020-07-15
down
wechat
bug