generation of a gene-corrected isogenic control ipsc line from cystic fibrosis patient-specific ipscs homozygous for p.phe508del mutation mediated by talens and ssodn

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ID: 207442
2017
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Abstract
Cystic fibrosis (CF) is a monogenetic disease caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene, which affects multiple organs. Human induced pluripotent stem cells (iPSCs) derived from CF patients and the generation of isogeneic gene-corrected control cell lines enable disease modelling, drug discovery or toxicological studies and therefore the development of CF patient-specific therapies. We have previously generated a hiPSC line from a CF patient homozygous for the p.Phe508del mutation. Here we used TALENs and single-stranded oligonucleotides to correct the mutated triplet in our CF-iPSC line.
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merkert2017stemgeneration Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors ;Sylvia Merkert;Christien Bednarski;Gudrun Göhring;Toni Cathomen;Ulrich Martin
Journal journal of energy chemistry
Year 2017
DOI
10.1016/j.scr.2017.07.010
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