| Literature DB >> 29444500 |
Yanlin Wang1, Changhe Shi1, Zhilei Wang1, Huifang Sun1, Zhihua Yang1, Fan Zhang2, Yutao Liu1, Han Liu1, Chenyang Jiang1, Shoutao Zhang3, Yuming Xu4, Xuejun Wen5.
Abstract
Spinocerebellar ataxia type 3 (SCA3) is a dominantly inherited neurodegenerative disease caused by a CAG repeat expansion in the region of the ATXN3 gene. The main feature of SCA3 is progressive ataxia, which affects balance, gait, and speech. Urine cells (UCs) of a SCA3 patient were successfully translated to induced pluripotent stem cells (iPSCs) by using the Sendai virus delivery system. ZZUi004-A cell line may provide a robust platform for further study of SCA3 pathogenesis as well as drug testing and gene therapy research.Entities:
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Year: 2018 PMID: 29444500 DOI: 10.1016/j.scr.2018.01.027
Source DB: PubMed Journal: Stem Cell Res ISSN: 1873-5061 Impact factor: 2.020