| pubmed-article:10549624 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:10549624 | lifeskim:mentions | umls-concept:C1456820 | lld:lifeskim |
| pubmed-article:10549624 | lifeskim:mentions | umls-concept:C0205263 | lld:lifeskim |
| pubmed-article:10549624 | lifeskim:mentions | umls-concept:C0679622 | lld:lifeskim |
| pubmed-article:10549624 | lifeskim:mentions | umls-concept:C0205314 | lld:lifeskim |
| pubmed-article:10549624 | lifeskim:mentions | umls-concept:C1334043 | lld:lifeskim |
| pubmed-article:10549624 | pubmed:issue | 4 | lld:pubmed |
| pubmed-article:10549624 | pubmed:dateCreated | 1999-11-23 | lld:pubmed |
| pubmed-article:10549624 | pubmed:abstractText | In a screen to identify genes induced by NF-kappaB/Rel transcription factors, we cloned a novel gene, b7h, that is a close homolog of B7 costimulatory ligands expressed on antigen-presenting cells. B7h can costimulate proliferation of purified T cells through a receptor on T cells distinct from CD28 or CTLA-4. Surprisingly, although B7h is expressed in unstimulated B cells, its expression is induced in both 3T3 cells and embryonic fibroblasts treated with TNFalpha, and it is upregulated in nonlymphoid tissues of mice treated with LPS, a potent activator of TNFalpha. These data define a novel costimulatory ligand for T cells and suggest that induction of B7h by TNFalpha may function as a mechanism to directly augment recognition of self during inflammation. | lld:pubmed |
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| pubmed-article:10549624 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:10549624 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:10549624 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:10549624 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:10549624 | pubmed:month | Oct | lld:pubmed |
| pubmed-article:10549624 | pubmed:issn | 1074-7613 | lld:pubmed |
| pubmed-article:10549624 | pubmed:author | pubmed-author:ShaW CWC | lld:pubmed |
| pubmed-article:10549624 | pubmed:author | pubmed-author:WallinJ JJJ | lld:pubmed |
| pubmed-article:10549624 | pubmed:author | pubmed-author:SwallowM MMM | lld:pubmed |
| pubmed-article:10549624 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:10549624 | pubmed:volume | 11 | lld:pubmed |
| pubmed-article:10549624 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:10549624 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:10549624 | pubmed:pagination | 423-32 | lld:pubmed |
| pubmed-article:10549624 | pubmed:dateRevised | 2011-11-17 | lld:pubmed |
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| pubmed-article:10549624 | pubmed:year | 1999 | lld:pubmed |
| pubmed-article:10549624 | pubmed:articleTitle | B7h, a novel costimulatory homolog of B7.1 and B7.2, is induced by TNFalpha. | lld:pubmed |
| pubmed-article:10549624 | pubmed:affiliation | Molecular and Cell Biology Department, University of California, Berkeley 94720, USA. | lld:pubmed |
| pubmed-article:10549624 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:10549624 | pubmed:publicationType | Comparative Study | lld:pubmed |
| pubmed-article:10549624 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
| pubmed-article:10549624 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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