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Generation of human induced pluripotent stem cell line (MUi026-A) from a patient with autosomal dominant polycystic kidney disease carrying PKD1 point mutation.
Maneepitasut, Warun; Wongkummool, Wasinee; Tong-Ngam, Pirut; Promthep, Kornkanok; Tubsuwan, Alisa; Khine Linn, Aung; Phakdeekitcharoen, Bunyong; Borwornpinyo, Suparerk; Kitiyanant, Narisorn; Phanthong, Phetcharat; Hongeng, Suradej.
Afiliação
  • Maneepitasut W; Molecular Medicine Program, Multidisciplinary Unit, Faculty of Science, Mahidol University, Bangkok 10400, Thailand.
  • Wongkummool W; Stem Cell Research Group, Institute of Molecular Biosciences, Mahidol University, Nakhon Pathom 73170, Thailand.
  • Tong-Ngam P; Stem Cell Research Group, Institute of Molecular Biosciences, Mahidol University, Nakhon Pathom 73170, Thailand.
  • Promthep K; Research Center for Neuroscience, Institute of Molecular Biosciences, Mahidol University, Nakhon Pathom 73170, Thailand.
  • Tubsuwan A; Stem Cell Research Group, Institute of Molecular Biosciences, Mahidol University, Nakhon Pathom 73170, Thailand.
  • Khine Linn A; Excellent Center for Drug Discovery, Faculty of Science, Mahidol University, Bangkok 10400 Thailand.
  • Phakdeekitcharoen B; Division of Nephrology, Department of Medicine, Faculty of Medicine, Ramathibodi Hospital, Mahidol University, Bangkok 10400, Thailand.
  • Borwornpinyo S; Excellent Center for Drug Discovery, Faculty of Science, Mahidol University, Bangkok 10400 Thailand; Department of Biotechnology, Faculty of Science, Mahidol University, Bangkok 10400, Thailand.
  • Kitiyanant N; Stem Cell Research Group, Institute of Molecular Biosciences, Mahidol University, Nakhon Pathom 73170, Thailand. Electronic address: narisorn.kit@mahidol.ac.th.
  • Phanthong P; Department of Anatomy, Faculty of Science, Mahidol University, Bangkok 10400, Thailand. Electronic address: phetcharat.pha@mahidol.edu.
  • Hongeng S; Department of Pediatrics, Faculty of Medicine, Ramathibodi Hospital, Mahidol University, Bangkok 10400, Thailand.
Stem Cell Res ; 53: 102306, 2021 05.
Article em En | MEDLINE | ID: mdl-33799277
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

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Rim Policístico Autossômico Dominante / Células-Tronco Pluripotentes Induzidas Limite: Female / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Rim Policístico Autossômico Dominante / Células-Tronco Pluripotentes Induzidas Limite: Female / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article