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Article: CD4 negative mice as a model for immunodeficiency.

TitleCD4 negative mice as a model for immunodeficiency.
Authors
Issue Date1993
Citation
Philosophical transactions of the Royal Society of London. Series B, Biological sciences, 1993, v. 342, n. 1299, p. 57-58 How to Cite?
AbstractCD4 is a co-receptor required for T cell helper functions. A mouse strain without CD4 expression has been generated. These animals, surprisingly have a normal CTL response and reduced, but not absent, humoral responses. A new population of MHC class II restricted CD4-CD8-TcR alpha beta+ T cells has emerged which possess helper function potential. These findings have important implications on disease situations where CD4 cells are decreased or absent.
Persistent Identifierhttp://hdl.handle.net/10722/292428
ISSN
2023 Impact Factor: 5.4
2023 SCImago Journal Rankings: 2.035
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorRahemtulla, A.-
dc.contributor.authorShahinian, A.-
dc.contributor.authorKundig, T.-
dc.contributor.authorZinkernagel, R.-
dc.contributor.authorMak, T. W.-
dc.date.accessioned2020-11-17T14:56:28Z-
dc.date.available2020-11-17T14:56:28Z-
dc.date.issued1993-
dc.identifier.citationPhilosophical transactions of the Royal Society of London. Series B, Biological sciences, 1993, v. 342, n. 1299, p. 57-58-
dc.identifier.issn0962-8436-
dc.identifier.urihttp://hdl.handle.net/10722/292428-
dc.description.abstractCD4 is a co-receptor required for T cell helper functions. A mouse strain without CD4 expression has been generated. These animals, surprisingly have a normal CTL response and reduced, but not absent, humoral responses. A new population of MHC class II restricted CD4-CD8-TcR alpha beta+ T cells has emerged which possess helper function potential. These findings have important implications on disease situations where CD4 cells are decreased or absent.-
dc.languageeng-
dc.relation.ispartofPhilosophical transactions of the Royal Society of London. Series B, Biological sciences-
dc.titleCD4 negative mice as a model for immunodeficiency.-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1098/rstb.1993.0135-
dc.identifier.pmid7904347-
dc.identifier.scopuseid_2-s2.0-0027925927-
dc.identifier.volume342-
dc.identifier.issue1299-
dc.identifier.spage57-
dc.identifier.epage58-
dc.identifier.isiWOS:A1993MH27700008-
dc.identifier.issnl0962-8436-

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