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Rh D blood group conversion using transcription activator-like effector nucleases

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dc.contributor.authorKim, Young-Hoon-
dc.contributor.authorKim, Hyun O.-
dc.contributor.authorBaek, Eun J.-
dc.contributor.authorKurita, Ryo-
dc.contributor.authorCha, Hyuk-Jin-
dc.contributor.authorNakamura, Yukio-
dc.contributor.authorKim, Hyongbum-
dc.date.accessioned2022-07-15T22:44:36Z-
dc.date.available2022-07-15T22:44:36Z-
dc.date.issued2015-06-
dc.identifier.issn2041-1723-
dc.identifier.issn2041-1723-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/157145-
dc.description.abstractGroup O D-negative blood cells are universal donors in transfusion medicine and methods for converting other blood groups into this universal donor group have been researched. However, conversion of D-positive cells into D-negative is yet to be achieved, although conversion of group A or B cells into O cells has been reported. The Rh D blood group is determined by the RHD gene, which encodes a 12-transmembrane domain protein. Here we convert Rh D-positive erythroid progenitor cells into D-negative cells using RHD-targeting transcription activator-like effector nucleases (TALENs). After transfection of TALEN-encoding plasmids, RHD-knockout clones are obtained. Erythroid-lineage cells differentiated from these knockout erythroid progenitor cells do not agglutinate in the presence of anti-D reagents and do not express D antigen, as assessed using flow cytometry. Our programmable nuclease-induced blood group conversion opens new avenues for compatible donor cell generation in transfusion medicine.-
dc.format.extent14-
dc.language영어-
dc.language.isoENG-
dc.publisherNature Publishing Group-
dc.titleRh D blood group conversion using transcription activator-like effector nucleases-
dc.typeArticle-
dc.publisher.location영국-
dc.identifier.doi10.1038/ncomms8451-
dc.identifier.scopusid2-s2.0-84935856216-
dc.identifier.wosid000357177100002-
dc.identifier.bibliographicCitationNature Communications, v.6, pp 1 - 14-
dc.citation.titleNature Communications-
dc.citation.volume6-
dc.citation.startPage1-
dc.citation.endPage14-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaScience & Technology - Other Topics-
dc.relation.journalWebOfScienceCategoryMultidisciplinary Sciences-
dc.subject.keywordPlusZINC-FINGER-
dc.subject.keywordPlusRNA SURVEILLANCE-
dc.subject.keywordPlusGENE-
dc.subject.keywordPlusCELLS-
dc.subject.keywordPlusENRICHMENT-
dc.subject.keywordPlusDISRUPTION-
dc.subject.keywordPlusMUTATION-
dc.subject.keywordPlusLIBRARY-
dc.subject.keywordPlusDISEASE-
dc.subject.keywordPlusPROTEIN-
dc.identifier.urlhttps://www.nature.com/articles/ncomms8451-
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서울 의과대학 (DEPARTMENT OF LABORATORY MEDICINE)
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