Publication:
Generation of human induced pluripotent stem cell line (MUi026-A) from a patient with autosomal dominant polycystic kidney disease carrying PKD1 point mutation

dc.contributor.authorWarun Maneepitasuten_US
dc.contributor.authorWasinee Wongkummoolen_US
dc.contributor.authorPirut Tong-ngamen_US
dc.contributor.authorKornkanok Promthepen_US
dc.contributor.authorAlisa Tubsuwanen_US
dc.contributor.authorAung Khine Linnen_US
dc.contributor.authorBunyong Phakdeekitcharoenen_US
dc.contributor.authorSuparerk Borwornpinyoen_US
dc.contributor.authorNarisorn Kitiyananten_US
dc.contributor.authorPhetcharat Phanthongen_US
dc.contributor.authorSuradej Hongengen_US
dc.contributor.otherRamathibodi Hospitalen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherInstitute of Molecular Biosciences, Mahidol Universityen_US
dc.date.accessioned2022-08-04T08:09:43Z
dc.date.available2022-08-04T08:09:43Z
dc.date.issued2021-05-01en_US
dc.description.abstractAutosomal 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.en_US
dc.identifier.citationStem Cell Research. Vol.53, (2021)en_US
dc.identifier.doi10.1016/j.scr.2021.102306en_US
dc.identifier.issn18767753en_US
dc.identifier.issn18735061en_US
dc.identifier.other2-s2.0-85104951634en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/76193
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85104951634&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.titleGeneration of human induced pluripotent stem cell line (MUi026-A) from a patient with autosomal dominant polycystic kidney disease carrying PKD1 point mutationen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85104951634&origin=inwarden_US

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