| Literature DB >> 28395808 |
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 Xu4, Yin-Xiong Li5.
Abstract
Urine resource cells were collected from a 59-year-old female patient with multiple endocrine neoplasia type 1 syndrome (MEN1) for generating iPS cells with episomal plasmids carrying Oct4, Sox2, Klf4 and miR-302-367. The patient sustained a heterozygous G>T transition mutation on the exon 9 of Men1 gene that was confirmed by sequencing analysis on the obtained iPSC lines. Karyotyping indicated the chromosomes with normal appearances and numbers. Their pluripotency was demonstrated by gene expression, as well as their abilities for differentiating into three germ layers. This cell line provides an ideal model for studying MEN1.Entities:
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Year: 2016 PMID: 28395808 DOI: 10.1016/j.scr.2016.12.009
Source DB: PubMed Journal: Stem Cell Res ISSN: 1873-5061 Impact factor: 2.020