Literature DB >> 28395795

Generation of a disease-specific iPS cell line derived from a patient with Charcot-Marie-Tooth type 2K lacking functional GDAP1 gene.

Salvador Martí1, Marian León2, Carmen Orellana3, Javier Prieto2, Xavier Ponsoda2, Carlos López-García2, Juan Jesús Vílchez4, Teresa Sevilla4, Josema Torres5.   

Abstract

Human CMT2-FiPS4F1 cell line was generated from fibroblasts of a patient with Charcot-Marie-Tooth disease harbouring the following mutations in the GDAP1 gene in heterozygosis: p.Q163X/p.T288NfsX3. This patient did not present mutations in the PM22, MPZ or GJB genes. Human reprogramming factors OCT3/4, KLF4, SOX2 and C-MYC were delivered using a non-integrative methodology that involves the use of Sendai virus.
Copyright © 2016 The Authors. Published by Elsevier B.V. All rights reserved.

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Year:  2016        PMID: 28395795     DOI: 10.1016/j.scr.2016.11.017

Source DB:  PubMed          Journal:  Stem Cell Res        ISSN: 1873-5061            Impact factor:   2.020


  1 in total

1.  Energy metabolism and mitochondrial defects in X-linked Charcot-Marie-Tooth (CMTX6) iPSC-derived motor neurons with the p.R158H PDK3 mutation.

Authors:  G Perez-Siles; A Cutrupi; M Ellis; R Screnci; D Mao; M Uesugi; Eppie M Yiu; Monique M Ryan; B O Choi; G Nicholson; M L Kennerson
Journal:  Sci Rep       Date:  2020-06-05       Impact factor: 4.379

  1 in total

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