Generation of a human fibroblast-derived induced pluripotent stem cell line KRIBBi009-A from a patient with breast cancer

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dc.contributor.authorNaeun Son-
dc.contributor.authorYe Seul Son-
dc.contributor.authorCho-Rok Jung-
dc.contributor.authorMi-Young Son-
dc.date.accessioned2023-03-18T16:33:15Z-
dc.date.available2023-03-18T16:33:15Z-
dc.date.issued2023-
dc.identifier.issn1873-5061-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/31381-
dc.description.abstractPatient-derived human induced pluripotent stem cells (iPSCs) provide a potentially useful resource for studying disease pathology and therapeutics. In this study, we generated the breast cancer patient-derived KRIBBi009-A-iPSC line from normal fibroblasts using the Sendai virus, which expressed pluripotent markers and exhibited differentiation capacity across 3 germ layers through in vitro differentiation and in vivo teratoma assay. A normal karyotype and the absence of cross-contamination of the cell lines were confirmed. Consequently, the developed iPSC line has been confirmed to be suitable for use in various studies.-
dc.publisherElsevier-
dc.titleGeneration of a human fibroblast-derived induced pluripotent stem cell line KRIBBi009-A from a patient with breast cancer-
dc.title.alternativeGeneration of a human fibroblast-derived induced pluripotent stem cell line KRIBBi009-A from a patient with breast cancer-
dc.typeArticle-
dc.citation.titleStem Cell Research-
dc.citation.number0-
dc.citation.endPage103060-
dc.citation.startPage103060-
dc.citation.volume68-
dc.contributor.affiliatedAuthorNaeun Son-
dc.contributor.affiliatedAuthorYe Seul Son-
dc.contributor.affiliatedAuthorCho-Rok Jung-
dc.contributor.affiliatedAuthorMi-Young Son-
dc.contributor.alternativeName손나은-
dc.contributor.alternativeName손예슬-
dc.contributor.alternativeName정초록-
dc.contributor.alternativeName손미영-
dc.identifier.bibliographicCitationStem Cell Research, vol. 68, pp. 103060-103060-
dc.identifier.doi10.1016/j.scr.2023.103060-
dc.description.journalClassY-
Appears in Collections:
Division of Research on National Challenges > Stem Cell Convergenece Research Center > 1. Journal Articles
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