Establishment of iPSC (KRIBBi001-A) from CD34+ group O D-negative bone marrow blood

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dc.contributor.authorJieun Kim-
dc.contributor.authorHyebin Koh-
dc.contributor.authorX Zhen-
dc.contributor.authorD S Lee-
dc.contributor.authorH Y Ha-
dc.contributor.authorJONG-HEE LEE-
dc.date.accessioned2021-02-26T08:36:01Z-
dc.date.available2021-02-26T08:36:01Z-
dc.date.issued2021-
dc.identifier.issn1873-5061-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/24142-
dc.description.abstractHuman induced pluripotent stem cells with indefinite propagation in vitro provide a potential donor source of cells including erythroid cells for human therapy. Since group O D-negative (RhD-) blood cells are considered as universal donors for transfusion, it is compelling to derive iPSC line from group O/RhD- sample as a new cellular source to generate universal RBCs. The resulting iPSC line derived from group O/RhD- somatic source showed typical features of pluripotent stem cells and could provide an unprecedented cellular tool to develop universal therapeutics for blood transfusion.-
dc.publisherElsevier-
dc.titleEstablishment of iPSC (KRIBBi001-A) from CD34+ group O D-negative bone marrow blood-
dc.title.alternativeEstablishment of iPSC (KRIBBi001-A) from CD34+ group O D-negative bone marrow blood-
dc.typeArticle-
dc.citation.titleStem Cell Research-
dc.citation.number0-
dc.citation.endPage102199-
dc.citation.startPage102199-
dc.citation.volume51-
dc.contributor.affiliatedAuthorJieun Kim-
dc.contributor.affiliatedAuthorHyebin Koh-
dc.contributor.affiliatedAuthorJONG-HEE LEE-
dc.contributor.alternativeName김지은-
dc.contributor.alternativeName고혜빈-
dc.contributor.alternativeNameZhen-
dc.contributor.alternativeName이동석-
dc.contributor.alternativeName하혜영-
dc.contributor.alternativeName이종희-
dc.identifier.bibliographicCitationStem Cell Research, vol. 51, pp. 102199-102199-
dc.identifier.doi10.1016/j.scr.2021.102199-
dc.description.journalClassY-
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Ochang Branch Institute > Division of National Bio-Infrastructure > National Primate Research Center > 1. Journal Articles
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