pubmed-article:11506195 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:11506195 | lifeskim:mentions | umls-concept:C0035820 | lld:lifeskim |
pubmed-article:11506195 | lifeskim:mentions | umls-concept:C0039194 | lld:lifeskim |
pubmed-article:11506195 | lifeskim:mentions | umls-concept:C0007578 | lld:lifeskim |
pubmed-article:11506195 | lifeskim:mentions | umls-concept:C0037083 | lld:lifeskim |
pubmed-article:11506195 | lifeskim:mentions | umls-concept:C1710082 | lld:lifeskim |
pubmed-article:11506195 | lifeskim:mentions | umls-concept:C1879547 | lld:lifeskim |
pubmed-article:11506195 | pubmed:issue | 4 | lld:pubmed |
pubmed-article:11506195 | pubmed:dateCreated | 2001-8-16 | lld:pubmed |
pubmed-article:11506195 | pubmed:abstractText | The T cell and antigen-presenting cell communicate to initiate an immune response through formation of an immunological synapse. This specialized cell-cell junction is compartmentalized into adhesion molecule and T cell receptor enriched regions or SMACs. Distinct signals seem to be generated in the T cell receptor and adhesion molecule-dominated regions. This review focuses on how these distinct signaling pathways may be integrated within the T cell to set thresholds for T cell activation, proliferation, and survival. | lld:pubmed |
pubmed-article:11506195 | pubmed:language | eng | lld:pubmed |
pubmed-article:11506195 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11506195 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:11506195 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11506195 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:11506195 | pubmed:month | Jul | lld:pubmed |
pubmed-article:11506195 | pubmed:issn | 0271-9142 | lld:pubmed |
pubmed-article:11506195 | pubmed:author | pubmed-author:DustinM LML | lld:pubmed |
pubmed-article:11506195 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:11506195 | pubmed:volume | 21 | lld:pubmed |
pubmed-article:11506195 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:11506195 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:11506195 | pubmed:pagination | 258-63 | lld:pubmed |
pubmed-article:11506195 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
pubmed-article:11506195 | pubmed:meshHeading | pubmed-meshheading:11506195... | lld:pubmed |
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pubmed-article:11506195 | pubmed:year | 2001 | lld:pubmed |
pubmed-article:11506195 | pubmed:articleTitle | Role of adhesion molecules in activation signaling in T lymphocytes. | lld:pubmed |
pubmed-article:11506195 | pubmed:affiliation | Department of Pathology, Skirball Institute of Molecular Medicine, New York University School of Medicine, New York 10016, USA. dustin@saturn.med.nyu.edu | lld:pubmed |
pubmed-article:11506195 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:11506195 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
pubmed-article:11506195 | pubmed:publicationType | Review | lld:pubmed |
pubmed-article:11506195 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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