| pubmed-article:9388192 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:9388192 | lifeskim:mentions | umls-concept:C1367307 | lld:lifeskim |
| pubmed-article:9388192 | lifeskim:mentions | umls-concept:C0034809 | lld:lifeskim |
| pubmed-article:9388192 | lifeskim:mentions | umls-concept:C1514762 | lld:lifeskim |
| pubmed-article:9388192 | lifeskim:mentions | umls-concept:C1551336 | lld:lifeskim |
| pubmed-article:9388192 | pubmed:issue | 49 | lld:pubmed |
| pubmed-article:9388192 | pubmed:dateCreated | 1998-1-8 | lld:pubmed |
| pubmed-article:9388192 | pubmed:abstractText | Interleukin-6 (IL-6) and glucocorticoids are important mediators of inflammatory and immunological responses. Glucocorticoids are known to synergistically enhance IL-6-mediated cellular responses. We now show that IL-6 also has a synergistic effect upon glucocorticoid signaling. In particular, IL-6-activated STAT3 associates with ligand-bound glucocorticoid receptor to form a transactivating/signaling complex, which can function through either an IL-6-responsive element or a glucocorticoid-responsive element. These findings reveal a new level of interaction between these two crucial signaling cascades and indicate that activated STAT3 can also act as a transcriptional co-activator without direct association with its DNA binding motif. | lld:pubmed |
| pubmed-article:9388192 | pubmed:language | eng | lld:pubmed |
| pubmed-article:9388192 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9388192 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:9388192 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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| pubmed-article:9388192 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9388192 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:9388192 | pubmed:month | Dec | lld:pubmed |
| pubmed-article:9388192 | pubmed:issn | 0021-9258 | lld:pubmed |
| pubmed-article:9388192 | pubmed:author | pubmed-author:JonesSS | lld:pubmed |
| pubmed-article:9388192 | pubmed:author | pubmed-author:FullerG MGM | lld:pubmed |
| pubmed-article:9388192 | pubmed:author | pubmed-author:ZhangZZ | lld:pubmed |
| pubmed-article:9388192 | pubmed:author | pubmed-author:FuentesN LNL | lld:pubmed |
| pubmed-article:9388192 | pubmed:author | pubmed-author:HagoodJ SJS | lld:pubmed |
| pubmed-article:9388192 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:9388192 | pubmed:day | 5 | lld:pubmed |
| pubmed-article:9388192 | pubmed:volume | 272 | lld:pubmed |
| pubmed-article:9388192 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:9388192 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:9388192 | pubmed:pagination | 30607-10 | lld:pubmed |
| pubmed-article:9388192 | pubmed:dateRevised | 2005-11-17 | lld:pubmed |
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| pubmed-article:9388192 | pubmed:meshHeading | pubmed-meshheading:9388192-... | lld:pubmed |
| pubmed-article:9388192 | pubmed:year | 1997 | lld:pubmed |
| pubmed-article:9388192 | pubmed:articleTitle | STAT3 acts as a co-activator of glucocorticoid receptor signaling. | lld:pubmed |
| pubmed-article:9388192 | pubmed:affiliation | Department of Cell Biology, Pulmonary Division, University of Alabama at Birmingham, Birmingham, Alabama 35294, USA. | lld:pubmed |
| pubmed-article:9388192 | pubmed:publicationType | Journal Article | lld:pubmed |
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