| pubmed-article:7799918 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:7799918 | lifeskim:mentions | umls-concept:C0086418 | lld:lifeskim |
| pubmed-article:7799918 | lifeskim:mentions | umls-concept:C0015576 | lld:lifeskim |
| pubmed-article:7799918 | lifeskim:mentions | umls-concept:C0221920 | lld:lifeskim |
| pubmed-article:7799918 | lifeskim:mentions | umls-concept:C0016030 | lld:lifeskim |
| pubmed-article:7799918 | lifeskim:mentions | umls-concept:C0033684 | lld:lifeskim |
| pubmed-article:7799918 | lifeskim:mentions | umls-concept:C0017337 | lld:lifeskim |
| pubmed-article:7799918 | lifeskim:mentions | umls-concept:C0205341 | lld:lifeskim |
| pubmed-article:7799918 | lifeskim:mentions | umls-concept:C0018270 | lld:lifeskim |
| pubmed-article:7799918 | lifeskim:mentions | umls-concept:C0598312 | lld:lifeskim |
| pubmed-article:7799918 | lifeskim:mentions | umls-concept:C0679058 | lld:lifeskim |
| pubmed-article:7799918 | lifeskim:mentions | umls-concept:C0679622 | lld:lifeskim |
| pubmed-article:7799918 | lifeskim:mentions | umls-concept:C1547699 | lld:lifeskim |
| pubmed-article:7799918 | lifeskim:mentions | umls-concept:C2700640 | lld:lifeskim |
| pubmed-article:7799918 | lifeskim:mentions | umls-concept:C0205314 | lld:lifeskim |
| pubmed-article:7799918 | lifeskim:mentions | umls-concept:C1519595 | lld:lifeskim |
| pubmed-article:7799918 | pubmed:issue | 1 | lld:pubmed |
| pubmed-article:7799918 | pubmed:dateCreated | 1995-1-24 | lld:pubmed |
| pubmed-article:7799918 | pubmed:databankReference | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:7799918 | pubmed:abstractText | We carried out subtractive enrichment of a cDNA library derived from mRNA of senescent human diploid fibroblasts (HDF) established from a subject with Werner syndrome of premature aging. By differential screening, we isolated an overexpressed cDNA sequence (S1-5) that codes for a novel protein containing epidermal growth factor (EGF)-like domains which match the EGF-like consensus sequences within several known extracellular proteins that play a role in cell growth, development, and cell signalling. S1-5 mRNA is overexpressed in Werner syndrome and senescent normal HDF, is induced by growth arrest of young normal cells, but is significantly decreased by high serum, conditions which promote cellular proliferation. Paradoxically, microinjection into young HDF of two different lengths of S1-5 mRNA, containing different putative AUG translational start sites, consistently stimulated rather than inhibited DNA synthesis by an apparent autocrine/paracrine mechanism. Thus, the S1-5 gene product may represent a negative and/or positive factor whose ultimate activity is modulated by the cell environment as occurs with other members of EGF-like family. | lld:pubmed |
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| pubmed-article:7799918 | pubmed:language | eng | lld:pubmed |
| pubmed-article:7799918 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:7799918 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:7799918 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:7799918 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:7799918 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:7799918 | pubmed:month | Jan | lld:pubmed |
| pubmed-article:7799918 | pubmed:issn | 0270-7306 | lld:pubmed |
| pubmed-article:7799918 | pubmed:author | pubmed-author:GoldsteinSS | lld:pubmed |
| pubmed-article:7799918 | pubmed:author | pubmed-author:LumpkinC... | lld:pubmed |
| pubmed-article:7799918 | pubmed:author | pubmed-author:Lecka-Czernik... | lld:pubmed |
| pubmed-article:7799918 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:7799918 | pubmed:volume | 15 | lld:pubmed |
| pubmed-article:7799918 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:7799918 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:7799918 | pubmed:pagination | 120-8 | lld:pubmed |
| pubmed-article:7799918 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
| pubmed-article:7799918 | pubmed:meshHeading | pubmed-meshheading:7799918-... | lld:pubmed |
| pubmed-article:7799918 | pubmed:meshHeading | pubmed-meshheading:7799918-... | lld:pubmed |
| pubmed-article:7799918 | pubmed:meshHeading | pubmed-meshheading:7799918-... | lld:pubmed |
| pubmed-article:7799918 | pubmed:meshHeading | pubmed-meshheading:7799918-... | lld:pubmed |
| pubmed-article:7799918 | pubmed:meshHeading | pubmed-meshheading:7799918-... | lld:pubmed |
