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dc.contributor.authorChanchao Lorthongpanichen_US
dc.contributor.authorChuti Laowtammathronen_US
dc.contributor.authorNittaya Jiamvoraphongen_US
dc.contributor.authorPimonwan Srisooken_US
dc.contributor.authorPimjai Chingsuwanroteen_US
dc.contributor.authorPhatchanat Klaihmonen_US
dc.contributor.authorSupaporn Waeteekulen_US
dc.contributor.authorYaowalak U-pratyaen_US
dc.contributor.authorSurapol Issaragrisilen_US
dc.contributor.otherFaculty of Medicine, Siriraj Hospital, Mahidol Universityen_US
dc.contributor.otherWattanosoth Hospitalen_US
dc.date.accessioned2020-08-25T09:01:00Z-
dc.date.available2020-08-25T09:01:00Z-
dc.date.issued2020-10-01en_US
dc.identifier.citationStem Cell Research. Vol.48, (2020)en_US
dc.identifier.issn18767753en_US
dc.identifier.issn18735061en_US
dc.identifier.other2-s2.0-85089190010en_US
dc.identifier.urihttp://repository.li.mahidol.ac.th/dspace/handle/123456789/57672-
dc.description.abstract© 2020 The Authors In mammals, there are a number of kinases, including serine/threonine-protein kinase LATS1, that act as a core kinase of the Hippo pathway and that negatively regulate the Hippo effector protein YAP and its paralog TAZ. Using CRISPR/Cas9 technology, we established a stable LATS1 knockdown (LATS1-KD) iPSC from the MUSIi012-A cell line. The LATS1-KD iPSC MUSIi012-A-3 that was developed maintained both the normal karyotype and the pluripotent phenotype, and retained the ability to differentiate into all three embryonic germ layers.en_US
dc.rightsMahidol Universityen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85089190010&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.titleGeneration of a serine/threonine-protein kinase LATS1 gene-edited iPSC MUSIi012-A-3en_US
dc.typeArticleen_US
dc.rights.holderSCOPUSen_US
dc.identifier.doi10.1016/j.scr.2020.101950en_US
dc.identifier.urlhttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85089190010&origin=inwarden_US
Appears in Collections:Scopus 2020

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