DC Field | Value | Language |
---|---|---|
dc.contributor.author | Notarangelo, LD | - |
dc.contributor.author | Kim, MS | - |
dc.contributor.author | Walter, JE | - |
dc.contributor.author | Lee, YN | - |
dc.date.accessioned | 2018-01-04T11:42:33Z | - |
dc.date.available | 2018-01-04T11:42:33Z | - |
dc.date.created | 2017-08-03 | - |
dc.date.issued | 2016-04 | - |
dc.identifier.issn | 1474-1733 | - |
dc.identifier.uri | https://oasis.postech.ac.kr/handle/2014.oak/39275 | - |
dc.description.abstract | The recombination-activating gene 1 (RAG1) and RAG2 proteins initiate the V(D)J recombination process, which ultimately enables the generation of T cells and B cells with a diversified repertoire of antigen-specific receptors. Mutations of the RAG genes in humans are associated with a broad spectrum of clinical phenotypes, ranging from severe combined immunodeficiency to autoimmunity. Recently, novel insights into the phenotypic diversity of this disease have been provided by resolving the crystal structure of the RAG complex, by developing novel assays to test recombination activity of the mutant RAG proteins and by characterizing the molecular and cellular basis of immune dysregulation in patients with RAG deficiency. | - |
dc.language | English | - |
dc.publisher | NATURE PUBLISHING GROUP | - |
dc.relation.isPartOf | NATURE REVIEWS IMMUNOLOGY | - |
dc.title | Human RAG mutations: biochemistry and clinical implications | - |
dc.type | Article | - |
dc.identifier.doi | 10.1038/NRI.2016.28 | - |
dc.type.rims | ART | - |
dc.identifier.bibliographicCitation | NATURE REVIEWS IMMUNOLOGY, v.4, no.4, pp.234 - 246 | - |
dc.identifier.wosid | 000372977200009 | - |
dc.date.tcdate | 2019-02-01 | - |
dc.citation.endPage | 246 | - |
dc.citation.number | 4 | - |
dc.citation.startPage | 234 | - |
dc.citation.title | NATURE REVIEWS IMMUNOLOGY | - |
dc.citation.volume | 4 | - |
dc.contributor.affiliatedAuthor | Kim, MS | - |
dc.identifier.scopusid | 2-s2.0-84961279265 | - |
dc.description.journalClass | 1 | - |
dc.description.journalClass | 1 | - |
dc.description.wostc | 42 | - |
dc.description.scptc | 30 | * |
dc.date.scptcdate | 2018-05-121 | * |
dc.description.isOpenAccess | N | - |
dc.type.docType | Review | - |
dc.subject.keywordPlus | SEVERE COMBINED IMMUNODEFICIENCY | - |
dc.subject.keywordPlus | COMBINED IMMUNE-DEFICIENCY | - |
dc.subject.keywordPlus | RECOMBINATION-ACTIVATING GENE | - |
dc.subject.keywordPlus | IMMUNOGLOBULIN-SECRETING CELLS | - |
dc.subject.keywordPlus | REGULATORY T-CELLS | - |
dc.subject.keywordPlus | OMENN-SYNDROME | - |
dc.subject.keywordPlus | V(D)J RECOMBINATION | - |
dc.subject.keywordPlus | B-CELL | - |
dc.subject.keywordPlus | RAG-1-DEFICIENT MICE | - |
dc.subject.keywordPlus | HOMOZYGOUS MUTATION | - |
dc.relation.journalWebOfScienceCategory | Immunology | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalResearchArea | Immunology | - |
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