| pubmed-article:3486423 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:3486423 | lifeskim:mentions | umls-concept:C0036536 | lld:lifeskim |
| pubmed-article:3486423 | lifeskim:mentions | umls-concept:C0036537 | lld:lifeskim |
| pubmed-article:3486423 | lifeskim:mentions | umls-concept:C0567416 | lld:lifeskim |
| pubmed-article:3486423 | lifeskim:mentions | umls-concept:C0039194 | lld:lifeskim |
| pubmed-article:3486423 | lifeskim:mentions | umls-concept:C0017262 | lld:lifeskim |
| pubmed-article:3486423 | lifeskim:mentions | umls-concept:C0220781 | lld:lifeskim |
| pubmed-article:3486423 | lifeskim:mentions | umls-concept:C1879547 | lld:lifeskim |
| pubmed-article:3486423 | pubmed:issue | 9 | lld:pubmed |
| pubmed-article:3486423 | pubmed:dateCreated | 1986-6-6 | lld:pubmed |
| pubmed-article:3486423 | pubmed:abstractText | The biosynthesis and expression of the tissue-specific class I molecule Qa-2 have been studied in resting and activated T-cell populations. Polyclonal activation of T lymphocytes induces a 3- to 4-fold increase in the biosynthesis of Qa-2 molecules but no increase in cell-surface levels. Analysis of the biosynthetic pathway of the Qa-2 molecule in activated lymphocytes reveals that approximately equal to 70% of the newly synthesized Qa-2 molecules are secreted as soluble molecules. In resting-cell populations, Qa-2 remains entirely cell-associated. This process is unique to the Qa-2 molecule, since other class I molecules (e.g., H-2Kb and H-2Db) synthesized by activated cells remain cell-associated. The possibility that the secreted Qa-2 molecule is the product of a new Qa gene or an alternatively spliced mRNA is considered. These results indicate that the Qa-2 molecules may not just function as a cell-surface recognition structure but also may serve a role as a soluble factor synthesized by activated lymphoid cell populations. | lld:pubmed |
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| pubmed-article:3486423 | pubmed:language | eng | lld:pubmed |
| pubmed-article:3486423 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:3486423 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:3486423 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:3486423 | pubmed:month | May | lld:pubmed |
| pubmed-article:3486423 | pubmed:issn | 0027-8424 | lld:pubmed |
| pubmed-article:3486423 | pubmed:author | pubmed-author:SoloskiM JMJ | lld:pubmed |
| pubmed-article:3486423 | pubmed:author | pubmed-author:EinhornGG | lld:pubmed |
| pubmed-article:3486423 | pubmed:author | pubmed-author:LattimoreAA | lld:pubmed |
| pubmed-article:3486423 | pubmed:author | pubmed-author:VernachioJJ | lld:pubmed |
| pubmed-article:3486423 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:3486423 | pubmed:volume | 83 | lld:pubmed |
| pubmed-article:3486423 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:3486423 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:3486423 | pubmed:pagination | 2949-53 | lld:pubmed |
| pubmed-article:3486423 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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| pubmed-article:3486423 | pubmed:year | 1986 | lld:pubmed |
| pubmed-article:3486423 | pubmed:articleTitle | Qa gene expression: biosynthesis and secretion of Qa-2 molecules in activated T cells. | lld:pubmed |
| pubmed-article:3486423 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:3486423 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
| pubmed-article:3486423 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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