Generation of human iPS cell line IBCHi001-A from dentatorubral-pallidoluysian atrophy patient's fibroblasts.
Stem Cell Res
; 39: 101512, 2019 08.
Article
em En
| MEDLINE
| ID: mdl-31374462
ABSTRACT
Dentatorubral-pallidoluysian atrophy (DRPLA) is an incurable autosomal dominant disease caused by an expansion of a CAG repeats in ATN1 gene encoding atrophin 1 protein. Here we report the generation of IBCHi001-A, an induced pluripotent stem cell (iPSC) line derived from DRPLA patient fibroblasts using non-integrative reprogramming technology with OCT4, SOX2, cMYC and KLF4 reprogramming factors. The pluripotency of iPSC was confirmed by immunocytochemistry and PCR for pluripotency markers and by the ability to form three germ layers in vitro. The established iPSC line offers a useful resource to study the pathogenesis of DPRLA.
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Base de dados:
MEDLINE
Assunto principal:
Epilepsias Mioclônicas Progressivas
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Células-Tronco Pluripotentes Induzidas
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Fibroblastos
Idioma:
En
Ano de publicação:
2019
Tipo de documento:
Article