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Stem Cell Res ; 53: 102306, 2021 05.
Artigo em Inglês | MEDLINE | ID: mdl-33799277

RESUMO

Autosomal dominant polycystic kidney disease (ADPKD) is one of the common genetic kidney disorders that are caused by mutations in PKD1 or PKD2 gene. In this report, the MUi026-A human induced pluripotent stem cell (hiPSC) line was established from the skin fibroblasts of a female ADPKD patient who had the PKD1 mutation with c.5878C > T. The iPSC line retained normal karyotype. The cells displayed embryonic stem cell-like characteristics with pluripotency marker expression and were able to differentiate into three germ layers.


Assuntos
Células-Tronco Pluripotentes Induzidas , Rim Policístico Autossômico Dominante , Feminino , Humanos , Mutação , Mutação Puntual , Rim Policístico Autossômico Dominante/genética , Canais de Cátion TRPP/genética
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