Publication:
An integration-free iPSC line (MUSIi008-A) derived from a patient with severe hemolytic anemia carrying compound heterozygote mutations in KLF1 gene for disease modeling

dc.contributor.authorPonthip Potiraten_US
dc.contributor.authorMethichit Wattanapanitchen_US
dc.contributor.authorVip Viprakasiten_US
dc.contributor.authorPakpoom Kheolamaien_US
dc.contributor.authorSurapol Issaragrisilen_US
dc.contributor.otherFaculty of Medicine, Thammasat Universityen_US
dc.contributor.otherFaculty of Medicine, Siriraj Hospital, Mahidol Universityen_US
dc.date.accessioned2020-01-27T07:55:50Z
dc.date.available2020-01-27T07:55:50Z
dc.date.issued2019-01-01en_US
dc.description.abstract© 2018 The Authors We generated an induced pluripotent stem cell (iPSC) line from peripheral blood mononuclear cells (PBMNCs) isolated from a 1-year old female carrying compound heterozygote for KLF1 mutations (G176RfsX179 and A298P mutations). Non-integrating Sendai viral (SeV) vectors containing KOS, hc-MYC and hKLF4 were used for reprogramming. The established MUSIi008-A cell line contained the same mutations found in the patient, expressed pluripotent markers, differentiated into cells of three embryonic germ layers both in vitro and in vivo, and exhibited normal karyotype. This cell line may provide an alternative renewable source of cells for in vitro disease modeling of severe transfusion-dependent hemolytic anemia.en_US
dc.identifier.citationStem Cell Research. Vol.34, (2019)en_US
dc.identifier.doi10.1016/j.scr.2018.09.021en_US
dc.identifier.issn18767753en_US
dc.identifier.issn18735061en_US
dc.identifier.other2-s2.0-85059233299en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/50364
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85059233299&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.titleAn integration-free iPSC line (MUSIi008-A) derived from a patient with severe hemolytic anemia carrying compound heterozygote mutations in KLF1 gene for disease modelingen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85059233299&origin=inwarden_US

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