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Generation of an induced pluripotent stem cell line (IUFi001) from a Cockayne syndrome patient carrying a mutation in the ERCC6 gene.
Martins, Soraia; Hacheney, Inken; Teichweyde, Nadine; Hildebrandt, Barbara; Krutmann, Jean; Rossi, Andrea.
Afiliação
  • Martins S; IUF-Leibniz Research Institute for Environmental Medicine, Duesseldorf, Germany.
  • Hacheney I; IUF-Leibniz Research Institute for Environmental Medicine, Duesseldorf, Germany.
  • Teichweyde N; IUF-Leibniz Research Institute for Environmental Medicine, Duesseldorf, Germany.
  • Hildebrandt B; Institute of Human Genetics, Medical Faculty, Heinrich-Heine-University Düsseldorf, Düsseldorf, Germany.
  • Krutmann J; IUF-Leibniz Research Institute for Environmental Medicine, Duesseldorf, Germany.
  • Rossi A; IUF-Leibniz Research Institute for Environmental Medicine, Duesseldorf, Germany. Electronic address: andrea.rossi@iuf-duesseldorf.de.
Stem Cell Res ; 55: 102456, 2021 08.
Article em En | MEDLINE | ID: mdl-34271225
Human fibroblasts from a Cockayne Syndrome (CS) patient carrying the compound heterozygous c.1131 A > T and c.2571C > T within ERCC Excision Repair 6 (ERCC6) were reprogramed to generate integration-free induced pluripotent stem cells (iPSCs). Characterization of IUFi001-iPSCs demonstrated that this iPSC line is free of exogenous reprogrammed genes and maintains the genomic integrity. The pluripotency of IUFi001-iPSCs was confirmed by the expression of the pluripotency-associated markers and by embryoid body-based differentiation into cell types representative of the three germ layers. The generated iPSC line provides a powerful tool to dissect the molecular mechanisms underlying CS caused by mutations within ERCC6.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Cockayne / Células-Tronco Pluripotentes Induzidas Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Cockayne / Células-Tronco Pluripotentes Induzidas Idioma: En Ano de publicação: 2021 Tipo de documento: Article