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Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
8
|
pubmed:dateCreated |
1996-12-3
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pubmed:abstractText |
To test the hypothesis that the expanded population of non-proliferative CD28-CD8+ T cells in HIV disease have shortened telomeres, thereby providing evidence that increased rounds of CD8+ cell division occur during HIV disease, possibly leading to replicative senescence and exhaustion of CD8+ T-cell responses.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Jul
|
pubmed:issn |
0269-9370
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pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
10
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
|
pubmed:pagination |
F17-22
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:8828735-Antigens, CD28,
pubmed-meshheading:8828735-CD8-Positive T-Lymphocytes,
pubmed-meshheading:8828735-Cell Aging,
pubmed-meshheading:8828735-Cell Division,
pubmed-meshheading:8828735-DNA,
pubmed-meshheading:8828735-HIV Infections,
pubmed-meshheading:8828735-Humans,
pubmed-meshheading:8828735-Molecular Weight,
pubmed-meshheading:8828735-T-Lymphocyte Subsets,
pubmed-meshheading:8828735-Telomere
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pubmed:year |
1996
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pubmed:articleTitle |
Shortened telomeres in the expanded CD28-CD8+ cell subset in HIV disease implicate replicative senescence in HIV pathogenesis.
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pubmed:affiliation |
Department of Pathology and Laboratory Medicine, University of California Los Angeles (UCLA) School of Medicine 90095-1745, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
|