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| pubmed-article:20827463 | lifeskim:mentions | umls-concept:C1426330 | lld:lifeskim |
| pubmed-article:20827463 | lifeskim:mentions | umls-concept:C1428424 | lld:lifeskim |
| pubmed-article:20827463 | lifeskim:mentions | umls-concept:C1167622 | lld:lifeskim |
| pubmed-article:20827463 | lifeskim:mentions | umls-concept:C0243076 | lld:lifeskim |
| pubmed-article:20827463 | lifeskim:mentions | umls-concept:C0679932 | lld:lifeskim |
| pubmed-article:20827463 | lifeskim:mentions | umls-concept:C0332120 | lld:lifeskim |
| pubmed-article:20827463 | lifeskim:mentions | umls-concept:C1136161 | lld:lifeskim |
| pubmed-article:20827463 | lifeskim:mentions | umls-concept:C0599278 | lld:lifeskim |
| pubmed-article:20827463 | pubmed:issue | 4 | lld:pubmed |
| pubmed-article:20827463 | pubmed:dateCreated | 2010-11-16 | lld:pubmed |
| pubmed-article:20827463 | pubmed:abstractText | The h5-HT(7) receptor is subject to inactivation by risperidone and 9-OH-risperidone, apparently through a pseudo-irreversible complex formed between these drugs and the receptor. Although risperidone and 9-OH-risperidone ("inactivating antagonists") completely inactivate the receptor, only 50% of the receptors form a pseudo-irreversible complex with these drugs. | lld:pubmed |
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| pubmed-article:20827463 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:20827463 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:20827463 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:20827463 | pubmed:month | Dec | lld:pubmed |
| pubmed-article:20827463 | pubmed:issn | 1432-2072 | lld:pubmed |
| pubmed-article:20827463 | pubmed:author | pubmed-author:SmithCarolC | lld:pubmed |
| pubmed-article:20827463 | pubmed:author | pubmed-author:TeitlerMiltM | lld:pubmed |
| pubmed-article:20827463 | pubmed:author | pubmed-author:KleinMichael... | lld:pubmed |
| pubmed-article:20827463 | pubmed:author | pubmed-author:TooheyNicoleN | lld:pubmed |
| pubmed-article:20827463 | pubmed:author | pubmed-author:KnightJessica... | lld:pubmed |
| pubmed-article:20827463 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:20827463 | pubmed:volume | 212 | lld:pubmed |
| pubmed-article:20827463 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:20827463 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:20827463 | pubmed:pagination | 687-97 | lld:pubmed |
| pubmed-article:20827463 | pubmed:dateRevised | 2011-7-26 | lld:pubmed |
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| pubmed-article:20827463 | pubmed:meshHeading | pubmed-meshheading:20827463... | lld:pubmed |
| pubmed-article:20827463 | pubmed:year | 2010 | lld:pubmed |
| pubmed-article:20827463 | pubmed:articleTitle | Clozapine and other competitive antagonists reactivate risperidone-inactivated h5-HT7 receptors: radioligand binding and functional evidence for GPCR homodimer protomer interactions. | lld:pubmed |
| pubmed-article:20827463 | pubmed:affiliation | Center for Neuropharmacology & Neuroscience, Albany Medical College, 47 New Scotland Avenue, Albany, NY 12208, USA. teitlem@mail.amc.edu | lld:pubmed |
| pubmed-article:20827463 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:20827463 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |
| entrez-gene:3363 | entrezgene:pubmed | pubmed-article:20827463 | lld:entrezgene |
| http://linkedlifedata.com/r... | entrezgene:pubmed | pubmed-article:20827463 | lld:entrezgene |
