| Literature DB >> 29554588 |
Aarne Fleischer1, Iván M Lorenzo1, Esther Palomino1, Trond Aasen2, Fernando Gómez3, Miguel Servera4, Víctor J Asensio5, Víctor Gálvez5, Juan Carlos Izpisúa-Belmonte6, Daniel Bachiller7.
Abstract
Cystic Fibrosis (CF) is a monogenic, lethal disease caused by mutations in the cystic fibrosis transmembrane conductance (CFTR) gene. Here we report the production of CF-iPS cell lines from two different p.F508del homozygous female patients (Table 1). Two different primary cell types, skin fibroblasts and keratinocytes, were transfected with retroviral cocktails containing four: c-MYC, KLF4, OCT4 and SOX2 (MKOS) or three: KLF4, OCT4 and SOX2 (KOS) reprogramming factors. Two fibroblast-derived MKOS lines are described in the main text. The lines carry the p.F508del mutation, have a normal karyotype, express pluripotency markers and are able to differentiate into the three germ layers.Entities:
Mesh:
Year: 2018 PMID: 29554588 DOI: 10.1016/j.scr.2018.03.004
Source DB: PubMed Journal: Stem Cell Res ISSN: 1873-5061 Impact factor: 2.020