Your browser doesn't support javascript.
loading
Generation of transgene-free iPSC lines from three patients with Friedreich's ataxia (FRDA) carrying GAA triplet expansions in the first intron of FXN gene.
Kelekçi, Simge; Ugurlu-Çimen, Deniz; Demir, Ata Berk; Özçimen, Burcu; Burak Yildiz, Abdullah; Batuhan Karakus, Mehmet; Börklü Yücel, Esra; Önder, Tamer T.
Afiliação
  • Kelekçi S; School of Medicine, Koc University, Istanbul, Turkey.
  • Ugurlu-Çimen D; School of Medicine, Koc University, Istanbul, Turkey.
  • Demir AB; School of Medicine, Koc University, Istanbul, Turkey.
  • Özçimen B; School of Medicine, Koc University, Istanbul, Turkey.
  • Burak Yildiz A; School of Medicine, Koc University, Istanbul, Turkey.
  • Batuhan Karakus M; School of Medicine, Koc University, Istanbul, Turkey.
  • Börklü Yücel E; Diagnostic Center for Genetic Diseases, Koc University Hospital, Koc University, Istanbul, Turkey.
  • Önder TT; School of Medicine, Koc University, Istanbul, Turkey. Electronic address: tonder@ku.edu.tr.
Stem Cell Res ; 54: 102438, 2021 07.
Article em En | MEDLINE | ID: mdl-34214898
Friedreich's ataxia (FRDA) is a rare neurodegenerative disorder which is caused by triplet repeat expansion (GAA) in the first intron of FXN gene. In this present study, we generated induced pluripotent stem cells (iPSC) lines from fibroblasts of three unrelated FRDA patients using integration-free episomal vectors. All iPSC lines express the pluripotency markers such as OCT4 and SSEA4, display normal karyotypes and can differentiate into all three germ layers via in vivo teratoma formation assay.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ataxia de Friedreich / Proteínas de Ligação ao Ferro / Células-Tronco Pluripotentes Induzidas Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ataxia de Friedreich / Proteínas de Ligação ao Ferro / Células-Tronco Pluripotentes Induzidas Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article