pubmed-article:2563241 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:2563241 | lifeskim:mentions | umls-concept:C0002844 | lld:lifeskim |
pubmed-article:2563241 | lifeskim:mentions | umls-concept:C0017710 | lld:lifeskim |
pubmed-article:2563241 | lifeskim:mentions | umls-concept:C0041487 | lld:lifeskim |
pubmed-article:2563241 | lifeskim:mentions | umls-concept:C0017262 | lld:lifeskim |
pubmed-article:2563241 | lifeskim:mentions | umls-concept:C0600508 | lld:lifeskim |
pubmed-article:2563241 | lifeskim:mentions | umls-concept:C0086597 | lld:lifeskim |
pubmed-article:2563241 | lifeskim:mentions | umls-concept:C2349975 | lld:lifeskim |
pubmed-article:2563241 | lifeskim:mentions | umls-concept:C1627358 | lld:lifeskim |
pubmed-article:2563241 | pubmed:issue | 2 | lld:pubmed |
pubmed-article:2563241 | pubmed:dateCreated | 1989-3-7 | lld:pubmed |
pubmed-article:2563241 | pubmed:abstractText | A glucocorticoid response element of the tyrosine aminotransferase gene was demonstrated to mediate effects of androgen when located upstream of a heterologous promoter linked to the chloramphenicol acetyl transferase gene (CAT). | lld:pubmed |
pubmed-article:2563241 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:2563241 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:2563241 | pubmed:language | eng | lld:pubmed |
pubmed-article:2563241 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:2563241 | pubmed:citationSubset | AIM | lld:pubmed |
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pubmed-article:2563241 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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pubmed-article:2563241 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:2563241 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:2563241 | pubmed:month | Feb | lld:pubmed |
pubmed-article:2563241 | pubmed:issn | 0013-7227 | lld:pubmed |
pubmed-article:2563241 | pubmed:author | pubmed-author:TindallD JDJ | lld:pubmed |
pubmed-article:2563241 | pubmed:author | pubmed-author:SandsAA | lld:pubmed |
pubmed-article:2563241 | pubmed:author | pubmed-author:DenisonS HSH | lld:pubmed |
pubmed-article:2563241 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:2563241 | pubmed:volume | 124 | lld:pubmed |
pubmed-article:2563241 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:2563241 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:2563241 | pubmed:pagination | 1091-3 | lld:pubmed |
pubmed-article:2563241 | pubmed:dateRevised | 2008-11-21 | lld:pubmed |
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pubmed-article:2563241 | pubmed:meshHeading | pubmed-meshheading:2563241-... | lld:pubmed |
pubmed-article:2563241 | pubmed:meshHeading | pubmed-meshheading:2563241-... | lld:pubmed |
pubmed-article:2563241 | pubmed:meshHeading | pubmed-meshheading:2563241-... | lld:pubmed |
pubmed-article:2563241 | pubmed:year | 1989 | lld:pubmed |
pubmed-article:2563241 | pubmed:articleTitle | A tyrosine aminotransferase glucocorticoid response element also mediates androgen enhancement of gene expression. | lld:pubmed |
pubmed-article:2563241 | pubmed:affiliation | Department of Cell Biology, Baylor College of Medicine, Houston, Texas 77030. | lld:pubmed |
pubmed-article:2563241 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:2563241 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
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