| Literature DB >> 28395810 |
Dongsheng Guo1, Feima Wu1, Haikun Liu1, Ge Gao1, Shanglong Kou1, Fan Yang1, Nasir Abbas1, Tiancheng Zhou2, Xiujuan Cai2, Hui Zhang2, Dajiang Qin2, Jialiang Li3, Kecheng Xu3, Yin-Xiong Li4.
Abstract
Urine resource cells were collected from a 23-year-old male with multiple endocrine neoplasia type 1 syndrome (MEN1) for generating iPS cells with episomal plasmids. Two stable iPSC lines with free of episomal plasmid were established. The patient has a heterozygous G>T mutation on the exon 9 of Men1 gene that was confirmed by sequencing analysis on all resulted cell lines. Karyotyping indicated the chromosomes with normal appearances and numbers. Their pluripotency was demonstrated by gene expression and their abilities for differentiating into three germ layers. These iPSC lines provide valuable in vitro resources for pathological study on MEN1 syndrome.Entities:
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Year: 2016 PMID: 28395810 DOI: 10.1016/j.scr.2016.12.002
Source DB: PubMed Journal: Stem Cell Res ISSN: 1873-5061 Impact factor: 2.020