pubmed-article:11134322 | rdf:type | pubmed:Citation | lld:pubmed |
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pubmed-article:11134322 | lifeskim:mentions | umls-concept:C0019733 | lld:lifeskim |
pubmed-article:11134322 | lifeskim:mentions | umls-concept:C1704529 | lld:lifeskim |
pubmed-article:11134322 | lifeskim:mentions | umls-concept:C0034790 | lld:lifeskim |
pubmed-article:11134322 | lifeskim:mentions | umls-concept:C0030956 | lld:lifeskim |
pubmed-article:11134322 | lifeskim:mentions | umls-concept:C0036576 | lld:lifeskim |
pubmed-article:11134322 | lifeskim:mentions | umls-concept:C0162326 | lld:lifeskim |
pubmed-article:11134322 | lifeskim:mentions | umls-concept:C1704241 | lld:lifeskim |
pubmed-article:11134322 | lifeskim:mentions | umls-concept:C1515655 | lld:lifeskim |
pubmed-article:11134322 | pubmed:issue | 2 | lld:pubmed |
pubmed-article:11134322 | pubmed:dateCreated | 2001-1-4 | lld:pubmed |
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pubmed-article:11134322 | pubmed:databankReference | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11134322 | pubmed:abstractText | Using HLA-peptide tetrameric complexes, we isolated human T-cell lymphotrophic virus type 1 Tax peptide-specific CD8(+) T cells ex vivo. Antigen-specific amino acid motifs were identified in the T-cell receptor Vbeta CDR3 region of clonally expanded CD8(+) T cells. This result directly confirms the importance of the CDR3 region in determining the antigen specificity in vivo. | lld:pubmed |
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pubmed-article:11134322 | pubmed:language | eng | lld:pubmed |
pubmed-article:11134322 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11134322 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:11134322 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:11134322 | pubmed:month | Jan | lld:pubmed |
pubmed-article:11134322 | pubmed:issn | 0022-538X | lld:pubmed |
pubmed-article:11134322 | pubmed:author | pubmed-author:SaitoMM | lld:pubmed |
pubmed-article:11134322 | pubmed:author | pubmed-author:FurukawaYY | lld:pubmed |
pubmed-article:11134322 | pubmed:author | pubmed-author:SaitoAA | lld:pubmed |
pubmed-article:11134322 | pubmed:author | pubmed-author:OsameMM | lld:pubmed |
pubmed-article:11134322 | pubmed:author | pubmed-author:WeberJ NJN | lld:pubmed |
pubmed-article:11134322 | pubmed:author | pubmed-author:BanghamC RCR | lld:pubmed |
pubmed-article:11134322 | pubmed:author | pubmed-author:UsukuKK | lld:pubmed |
pubmed-article:11134322 | pubmed:author | pubmed-author:TaylorG PGP | lld:pubmed |
pubmed-article:11134322 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:11134322 | pubmed:volume | 75 | lld:pubmed |
pubmed-article:11134322 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:11134322 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:11134322 | pubmed:pagination | 1065-71 | lld:pubmed |
pubmed-article:11134322 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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pubmed-article:11134322 | pubmed:meshHeading | pubmed-meshheading:11134322... | lld:pubmed |
pubmed-article:11134322 | pubmed:year | 2001 | lld:pubmed |
pubmed-article:11134322 | pubmed:articleTitle | In vivo selection of T-cell receptor junctional region sequences by HLA-A2 human T-cell lymphotropic virus type 1 Tax11-19 peptide complexes. | lld:pubmed |
pubmed-article:11134322 | pubmed:affiliation | Departments of Immunology, Imperial College School of Medicine, St. Mary's Campus, London W2 1PG, United Kingdom. | lld:pubmed |
pubmed-article:11134322 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:11134322 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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