Warun ManeepitasutWasinee WongkummoolPirut Tong-ngamKornkanok PromthepAlisa TubsuwanAung Khine LinnBunyong PhakdeekitcharoenSuparerk BorwornpinyoNarisorn KitiyanantPhetcharat PhanthongSuradej HongengRamathibodi HospitalMahidol UniversityInstitute of Molecular Biosciences, Mahidol University2022-08-042022-08-042021-05-01Stem Cell Research. Vol.53, (2021)18767753187350612-s2.0-85104951634https://repository.li.mahidol.ac.th/handle/20.500.14594/76193Autosomal 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.Mahidol UniversityBiochemistry, Genetics and Molecular BiologyArticleSCOPUS10.1016/j.scr.2021.102306