DC Field | Value | Language |
---|---|---|
dc.contributor.author | Jieun Kim | - |
dc.contributor.author | Hyebin Koh | - |
dc.contributor.author | X Zhen | - |
dc.contributor.author | D S Lee | - |
dc.contributor.author | H Y Ha | - |
dc.contributor.author | JONG-HEE LEE | - |
dc.date.accessioned | 2021-02-26T08:36:01Z | - |
dc.date.available | 2021-02-26T08:36:01Z | - |
dc.date.issued | 2021 | - |
dc.identifier.issn | 1873-5061 | - |
dc.identifier.uri | https://oak.kribb.re.kr/handle/201005/24142 | - |
dc.description.abstract | Human 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.publisher | Elsevier | - |
dc.title | Establishment of iPSC (KRIBBi001-A) from CD34+ group O D-negative bone marrow blood | - |
dc.title.alternative | Establishment of iPSC (KRIBBi001-A) from CD34+ group O D-negative bone marrow blood | - |
dc.type | Article | - |
dc.citation.title | Stem Cell Research | - |
dc.citation.number | 0 | - |
dc.citation.endPage | 102199 | - |
dc.citation.startPage | 102199 | - |
dc.citation.volume | 51 | - |
dc.contributor.affiliatedAuthor | Jieun Kim | - |
dc.contributor.affiliatedAuthor | Hyebin Koh | - |
dc.contributor.affiliatedAuthor | JONG-HEE LEE | - |
dc.contributor.alternativeName | 김지은 | - |
dc.contributor.alternativeName | 고혜빈 | - |
dc.contributor.alternativeName | Zhen | - |
dc.contributor.alternativeName | 이동석 | - |
dc.contributor.alternativeName | 하혜영 | - |
dc.contributor.alternativeName | 이종희 | - |
dc.identifier.bibliographicCitation | Stem Cell Research, vol. 51, pp. 102199-102199 | - |
dc.identifier.doi | 10.1016/j.scr.2021.102199 | - |
dc.description.journalClass | Y | - |
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