Statements in which the resource exists.
SubjectPredicateObjectContext
pubmed-article:10047459rdf:typepubmed:Citationlld:pubmed
pubmed-article:10047459lifeskim:mentionsumls-concept:C1705522lld:lifeskim
pubmed-article:10047459lifeskim:mentionsumls-concept:C0007581lld:lifeskim
pubmed-article:10047459lifeskim:mentionsumls-concept:C0288472lld:lifeskim
pubmed-article:10047459lifeskim:mentionsumls-concept:C1704675lld:lifeskim
pubmed-article:10047459lifeskim:mentionsumls-concept:C1711300lld:lifeskim
pubmed-article:10047459lifeskim:mentionsumls-concept:C0376558lld:lifeskim
pubmed-article:10047459lifeskim:mentionsumls-concept:C0249197lld:lifeskim
pubmed-article:10047459lifeskim:mentionsumls-concept:C1420626lld:lifeskim
pubmed-article:10047459lifeskim:mentionsumls-concept:C1704259lld:lifeskim
pubmed-article:10047459lifeskim:mentionsumls-concept:C0205396lld:lifeskim
pubmed-article:10047459lifeskim:mentionsumls-concept:C1705987lld:lifeskim
pubmed-article:10047459lifeskim:mentionsumls-concept:C0851285lld:lifeskim
pubmed-article:10047459lifeskim:mentionsumls-concept:C2700613lld:lifeskim
pubmed-article:10047459pubmed:issue1lld:pubmed
pubmed-article:10047459pubmed:dateCreated1999-3-17lld:pubmed
pubmed-article:10047459pubmed:abstractTextThe p21((Cip1/Waf1/Sdi1)) protein is a cyclin-dependent kinase inhibitor that is induced in normal human fibroblasts (NHF) following DNA damage, following serum stimulation, and at cellular senescence. Expression of the human papilloma virus 16 E6 oncoprotein in NHF cells results in the loss of the p21 protein, independent of mRNA level under most conditions. The p21 protein levels in NHF-E6 cells remained low following DNA damage or serum stimulation even though mRNA levels increased. In contrast, the p21 protein was transiently induced in NHF-E6 cells at the onset of cellular senescence. Expression of the E6 oncoprotein in transformed cells had no effect on p21 protein levels. This demonstrates that two posttranscriptional pathways regulate expression of p21 protein in NHF cells under different conditions. Disruption of posttranscriptional regulation is correlated with extension of life span, altered cell fate, and transformation.lld:pubmed
pubmed-article:10047459pubmed:languageenglld:pubmed
pubmed-article:10047459pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:10047459pubmed:citationSubsetIMlld:pubmed
pubmed-article:10047459pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:10047459pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:10047459pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:10047459pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:10047459pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:10047459pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:10047459pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:10047459pubmed:statusMEDLINElld:pubmed
pubmed-article:10047459pubmed:monthFeblld:pubmed
pubmed-article:10047459pubmed:issn0014-4827lld:pubmed
pubmed-article:10047459pubmed:authorpubmed-author:BarrettJ CJClld:pubmed
pubmed-article:10047459pubmed:authorpubmed-author:ChiaoCClld:pubmed
pubmed-article:10047459pubmed:authorpubmed-author:BurkhartB ABAlld:pubmed
pubmed-article:10047459pubmed:authorpubmed-author:AlcortaD ADAlld:pubmed
pubmed-article:10047459pubmed:authorpubmed-author:IsaacsJ SJSlld:pubmed
pubmed-article:10047459pubmed:issnTypePrintlld:pubmed
pubmed-article:10047459pubmed:day25lld:pubmed
pubmed-article:10047459pubmed:volume247lld:pubmed
pubmed-article:10047459pubmed:ownerNLMlld:pubmed
pubmed-article:10047459pubmed:authorsCompleteYlld:pubmed
pubmed-article:10047459pubmed:pagination168-75lld:pubmed
pubmed-article:10047459pubmed:dateRevised2006-11-15lld:pubmed
pubmed-article:10047459pubmed:meshHeadingpubmed-meshheading:10047459...lld:pubmed
pubmed-article:10047459pubmed:meshHeadingpubmed-meshheading:10047459...lld:pubmed
pubmed-article:10047459pubmed:meshHeadingpubmed-meshheading:10047459...lld:pubmed
pubmed-article:10047459pubmed:meshHeadingpubmed-meshheading:10047459...lld:pubmed
pubmed-article:10047459pubmed:meshHeadingpubmed-meshheading:10047459...lld:pubmed
pubmed-article:10047459pubmed:meshHeadingpubmed-meshheading:10047459...lld:pubmed
pubmed-article:10047459pubmed:meshHeadingpubmed-meshheading:10047459...lld:pubmed
pubmed-article:10047459pubmed:meshHeadingpubmed-meshheading:10047459...lld:pubmed
pubmed-article:10047459pubmed:meshHeadingpubmed-meshheading:10047459...lld:pubmed
pubmed-article:10047459pubmed:meshHeadingpubmed-meshheading:10047459...lld:pubmed
pubmed-article:10047459pubmed:meshHeadingpubmed-meshheading:10047459...lld:pubmed
pubmed-article:10047459pubmed:meshHeadingpubmed-meshheading:10047459...lld:pubmed
pubmed-article:10047459pubmed:year1999lld:pubmed
pubmed-article:10047459pubmed:articleTitleTwo posttranscriptional pathways that regulate p21(Cip1/Waf1/Sdi1) are identified by HPV16-E6 interaction and correlate with life span and cellular senescence.lld:pubmed
pubmed-article:10047459pubmed:affiliationLaboratory of Molecular Carcinogenesis, National Institute of Environmental Health Science, Research Triangle Park, North Carolina, 27709, USA.lld:pubmed
pubmed-article:10047459pubmed:publicationTypeJournal Articlelld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:10047459lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:10047459lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:10047459lld:pubmed