| Literature DB >> 30611022 |
Ying-Qian Lu1, En-Lin Dong1, Wei-Qi Yang2, Lu-Lu Lai1, Xiao-Hong Lin1, Li-Xiang Ma2, Wan-Jin Chen3, Ning Wang3, Xiang Lin4.
Abstract
The human iPS cell line, hiPS-SPG76 (FJMUi001-A), derived from skin fibroblasts from a 42-year-old male hereditary spastic paraplegia patient carrying compound heterozygous p.P498L (c.1493C > T) and p.R618W (c.1852C > T) mutations in the CAPN1 gene, was generated by non-integrative reprogramming vectors encoding OCT3/4, SOX2, KLF4, and c-MYC. The established hiPS-SPG76 was free of genomically integrated reprogramming genes, had a normal karyotype, expressed pluripotency markers, and had capacity to form three germ layers in vitro and in vivo. This generated hiPS cell line offers a useful resource to study the pathogenesis of SPG76.Entities:
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Year: 2018 PMID: 30611022 DOI: 10.1016/j.scr.2018.11.015
Source DB: PubMed Journal: Stem Cell Res ISSN: 1873-5061 Impact factor: 2.020