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pubmed-article:20948629rdf:typepubmed:Citationlld:pubmed
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pubmed-article:20948629pubmed:dateCreated2010-10-15lld:pubmed
pubmed-article:20948629pubmed:abstractTextIn recent studies, two distinct mechanisms have been proposed to account for major histocompatibility complex (MHC) restriction of T-cell activity: (a) evolution-driven interactions between T-cell receptor (TCR) variable regions and MHC, and (b) a requirement for CD4 or CD8 binding to MHC to initiate signalling through the TCR complex. Both mechanisms are likely to be essential, but for different reasons.lld:pubmed
pubmed-article:20948629pubmed:languageenglld:pubmed
pubmed-article:20948629pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:20948629pubmed:statusPubMed-not-MEDLINElld:pubmed
pubmed-article:20948629pubmed:issn1757-594Xlld:pubmed
pubmed-article:20948629pubmed:authorpubmed-author:KranzDavid...lld:pubmed
pubmed-article:20948629pubmed:issnTypeElectroniclld:pubmed
pubmed-article:20948629pubmed:volume1lld:pubmed
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pubmed-article:20948629pubmed:pagination55lld:pubmed
pubmed-article:20948629pubmed:year2009lld:pubmed
pubmed-article:20948629pubmed:articleTitleTwo mechanisms that account for major histocompatibility complex restriction of T cells.lld:pubmed
pubmed-article:20948629pubmed:affiliationDepartment of Biochemistry, University of Illinois 600 South Mathews Avenue, Urbana-Champaign, IL 61801 USA. d-kranz@illinois.edulld:pubmed
pubmed-article:20948629pubmed:publicationTypeJournal Articlelld:pubmed