| pubmed-article:1309938 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:1309938 | lifeskim:mentions | umls-concept:C0020971 | lld:lifeskim |
| pubmed-article:1309938 | lifeskim:mentions | umls-concept:C0337611 | lld:lifeskim |
| pubmed-article:1309938 | lifeskim:mentions | umls-concept:C0003069 | lld:lifeskim |
| pubmed-article:1309938 | lifeskim:mentions | umls-concept:C0030956 | lld:lifeskim |
| pubmed-article:1309938 | lifeskim:mentions | umls-concept:C0205419 | lld:lifeskim |
| pubmed-article:1309938 | lifeskim:mentions | umls-concept:C1283195 | lld:lifeskim |
| pubmed-article:1309938 | pubmed:issue | 6357 | lld:pubmed |
| pubmed-article:1309938 | pubmed:dateCreated | 1992-2-18 | lld:pubmed |
| pubmed-article:1309938 | pubmed:abstractText | To test models of T-cell recognition, mice transgenic for T-cell receptor alpha or beta chain have been immunized with variant peptides that force changes in the resulting T-cell response. In particular, charge substitutions on the peptide often elicit reciprocal charges in the junctional (CDR3) sequences of T-cell receptor V alpha or V beta chains, indicating direct T-cell receptor-peptide contact, and allowing derivation of a topology for the T-cell receptor-MHC interaction. At one position on the peptide, variants transformed a homogeneous V beta response into a very heterogeneous one. | lld:pubmed |
| pubmed-article:1309938 | pubmed:language | eng | lld:pubmed |
| pubmed-article:1309938 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:1309938 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:1309938 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:1309938 | pubmed:month | Jan | lld:pubmed |
| pubmed-article:1309938 | pubmed:issn | 0028-0836 | lld:pubmed |
| pubmed-article:1309938 | pubmed:author | pubmed-author:EsserUU | lld:pubmed |
| pubmed-article:1309938 | pubmed:author | pubmed-author:DavisM MMM | lld:pubmed |
| pubmed-article:1309938 | pubmed:author | pubmed-author:PORTEOUSDD | lld:pubmed |
| pubmed-article:1309938 | pubmed:author | pubmed-author:ReayP APA | lld:pubmed |
| pubmed-article:1309938 | pubmed:author | pubmed-author:JorgensenJ... | lld:pubmed |
| pubmed-article:1309938 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:1309938 | pubmed:day | 16 | lld:pubmed |
| pubmed-article:1309938 | pubmed:volume | 355 | lld:pubmed |
| pubmed-article:1309938 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:1309938 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:1309938 | pubmed:pagination | 224-30 | lld:pubmed |
| pubmed-article:1309938 | pubmed:dateRevised | 2008-11-21 | lld:pubmed |
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| pubmed-article:1309938 | pubmed:year | 1992 | lld:pubmed |
| pubmed-article:1309938 | pubmed:articleTitle | Mapping T-cell receptor-peptide contacts by variant peptide immunization of single-chain transgenics. | lld:pubmed |
| pubmed-article:1309938 | pubmed:affiliation | Department of Microbiology and Immunology, Stanford University, California 94305. | lld:pubmed |
| pubmed-article:1309938 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:1309938 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
| pubmed-article:1309938 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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