| pubmed-article:8324824 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:8324824 | lifeskim:mentions | umls-concept:C0040300 | lld:lifeskim |
| pubmed-article:8324824 | lifeskim:mentions | umls-concept:C1171362 | lld:lifeskim |
| pubmed-article:8324824 | lifeskim:mentions | umls-concept:C0597298 | lld:lifeskim |
| pubmed-article:8324824 | lifeskim:mentions | umls-concept:C0017262 | lld:lifeskim |
| pubmed-article:8324824 | lifeskim:mentions | umls-concept:C0013138 | lld:lifeskim |
| pubmed-article:8324824 | lifeskim:mentions | umls-concept:C1515670 | lld:lifeskim |
| pubmed-article:8324824 | lifeskim:mentions | umls-concept:C1326579 | lld:lifeskim |
| pubmed-article:8324824 | lifeskim:mentions | umls-concept:C0058913 | lld:lifeskim |
| pubmed-article:8324824 | pubmed:issue | 7 | lld:pubmed |
| pubmed-article:8324824 | pubmed:dateCreated | 1993-8-12 | lld:pubmed |
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| pubmed-article:8324824 | pubmed:abstractText | In D. melanogaster a pulse of the steroid hormone ecdysone triggers the larval-to-adult metamorphosis, a complex process in which this hormone induces imaginal tissues to generate adult structures and larval tissues to degenerate. We show that the EcR gene encodes three ecdysone receptor isoforms (EcR-A, EcR-B1, and EcR-B2) that have common DNA- and hormone-binding domains but different N-terminal regions. We have used isoform-specific monoclonal antibodies to show that at the onset of metamorphosis different ecdysone target tissues express different isoform combinations in a manner consistent with the proposition that the different metamorphic responses of these tissues require different combinations of the EcR isoforms. We have also determined temporal developmental profiles of the EcR isoforms and their mRNAs in whole animals, showing that different isoforms predominate at different developmental stages that are marked by a pulse of ecdysone. | lld:pubmed |
| pubmed-article:8324824 | pubmed:language | eng | lld:pubmed |
| pubmed-article:8324824 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:8324824 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:8324824 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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| pubmed-article:8324824 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:8324824 | pubmed:month | Jul | lld:pubmed |
| pubmed-article:8324824 | pubmed:issn | 0092-8674 | lld:pubmed |
| pubmed-article:8324824 | pubmed:author | pubmed-author:SwyrydE AEA | lld:pubmed |
| pubmed-article:8324824 | pubmed:author | pubmed-author:HognessD SDS | lld:pubmed |
| pubmed-article:8324824 | pubmed:author | pubmed-author:TalbotW SWS | lld:pubmed |
| pubmed-article:8324824 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:8324824 | pubmed:day | 2 | lld:pubmed |
| pubmed-article:8324824 | pubmed:volume | 73 | lld:pubmed |
| pubmed-article:8324824 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:8324824 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:8324824 | pubmed:pagination | 1323-37 | lld:pubmed |
| pubmed-article:8324824 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
| pubmed-article:8324824 | pubmed:meshHeading | pubmed-meshheading:8324824-... | lld:pubmed |
| pubmed-article:8324824 | pubmed:meshHeading | pubmed-meshheading:8324824-... | lld:pubmed |
| pubmed-article:8324824 | pubmed:meshHeading | pubmed-meshheading:8324824-... | lld:pubmed |
| pubmed-article:8324824 | pubmed:meshHeading | pubmed-meshheading:8324824-... | lld:pubmed |
| pubmed-article:8324824 | pubmed:meshHeading | pubmed-meshheading:8324824-... | lld:pubmed |
| pubmed-article:8324824 | pubmed:meshHeading | pubmed-meshheading:8324824-... | lld:pubmed |
| pubmed-article:8324824 | pubmed:meshHeading | pubmed-meshheading:8324824-... | lld:pubmed |
| pubmed-article:8324824 | pubmed:meshHeading | pubmed-meshheading:8324824-... | lld:pubmed |
| pubmed-article:8324824 | pubmed:meshHeading | pubmed-meshheading:8324824-... | lld:pubmed |
| pubmed-article:8324824 | pubmed:meshHeading | pubmed-meshheading:8324824-... | lld:pubmed |
| pubmed-article:8324824 | pubmed:year | 1993 | lld:pubmed |
| pubmed-article:8324824 | pubmed:articleTitle | Drosophila tissues with different metamorphic responses to ecdysone express different ecdysone receptor isoforms. | lld:pubmed |
| pubmed-article:8324824 | pubmed:affiliation | Department of Biochemistry, Stanford University School of Medicine, California 94305. | lld:pubmed |
| pubmed-article:8324824 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:8324824 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
| pubmed-article:8324824 | pubmed:publicationType | Research Support, U.S. Gov't, Non-P.H.S. | lld:pubmed |
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