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Rh D blood group conversion using transcription activator-like effector nucleases
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Kim, Young-Hoon | - |
| dc.contributor.author | Kim, Hyun O. | - |
| dc.contributor.author | Baek, Eun J. | - |
| dc.contributor.author | Kurita, Ryo | - |
| dc.contributor.author | Cha, Hyuk-Jin | - |
| dc.contributor.author | Nakamura, Yukio | - |
| dc.contributor.author | Kim, Hyongbum | - |
| dc.date.accessioned | 2022-07-15T22:44:36Z | - |
| dc.date.available | 2022-07-15T22:44:36Z | - |
| dc.date.issued | 2015-06 | - |
| dc.identifier.issn | 2041-1723 | - |
| dc.identifier.issn | 2041-1723 | - |
| dc.identifier.uri | https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/157145 | - |
| dc.description.abstract | Group 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.extent | 14 | - |
| dc.language | 영어 | - |
| dc.language.iso | ENG | - |
| dc.publisher | Nature Publishing Group | - |
| dc.title | Rh D blood group conversion using transcription activator-like effector nucleases | - |
| dc.type | Article | - |
| dc.publisher.location | 영국 | - |
| dc.identifier.doi | 10.1038/ncomms8451 | - |
| dc.identifier.scopusid | 2-s2.0-84935856216 | - |
| dc.identifier.wosid | 000357177100002 | - |
| dc.identifier.bibliographicCitation | Nature Communications, v.6, pp 1 - 14 | - |
| dc.citation.title | Nature Communications | - |
| dc.citation.volume | 6 | - |
| dc.citation.startPage | 1 | - |
| dc.citation.endPage | 14 | - |
| dc.type.docType | Article | - |
| dc.description.isOpenAccess | N | - |
| dc.description.journalRegisteredClass | sci | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalResearchArea | Science & Technology - Other Topics | - |
| dc.relation.journalWebOfScienceCategory | Multidisciplinary Sciences | - |
| dc.subject.keywordPlus | ZINC-FINGER | - |
| dc.subject.keywordPlus | RNA SURVEILLANCE | - |
| dc.subject.keywordPlus | GENE | - |
| dc.subject.keywordPlus | CELLS | - |
| dc.subject.keywordPlus | ENRICHMENT | - |
| dc.subject.keywordPlus | DISRUPTION | - |
| dc.subject.keywordPlus | MUTATION | - |
| dc.subject.keywordPlus | LIBRARY | - |
| dc.subject.keywordPlus | DISEASE | - |
| dc.subject.keywordPlus | PROTEIN | - |
| dc.identifier.url | https://www.nature.com/articles/ncomms8451 | - |
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