| Literature DB >> 27345792 |
Alisa Tubsuwan1, Carlota Pires2, Mikkel A Rasmussen3, Benjamin Schmid3, Jørgen E Nielsen4, Lena E Hjermind4, Vanessa Hall2, Troels T Nielsen4, Gunhild Waldemar4, Poul Hyttel2, Christian Clausen3, Narisorn Kitiyanant1, Kristine K Freude2, Bjørn Holst3.
Abstract
Induced pluripotent stem cells (iPSCs) were generated from skin fibroblasts isolated from a 58-year old male with a L150P mutation in the presenilin 1 (PSEN-1) gene, which is responsible for the majority of familial cases of Alzheimer's disease (AD). The iPSCs were established by co-electroporation with episomal plasmids containing hOCT4, hSOX2, hL-MYC, hKLF4, hNANOG, hLIN28, and short hairpin RNA against TP53. The iPSCs contained the specific heterozygous mutation c.449C>T, had normal karyotype, expressed the expected pluripotency genes and displayed in vitro differentiation potential to the three germ layers. The iPSCs may be useful for studying familial AD pathology in vitro.Entities:
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Year: 2015 PMID: 27345792 DOI: 10.1016/j.scr.2015.12.015
Source DB: PubMed Journal: Stem Cell Res ISSN: 1873-5061 Impact factor: 2.020