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Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/12643
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dc.contributor.authorBeart, P Men
dc.date.accessioned2015-05-16T02:22:10Z
dc.date.available2015-05-16T02:22:10Z
dc.date.issued1989-06-01en
dc.identifier.citationClinical and Experimental Pharmacology & Physiology; 16(6): 511-5en
dc.identifier.govdoc2569952en
dc.identifier.otherPUBMEDen
dc.identifier.urihttp://ahro.austin.org.au/austinjspui/handle/1/12643en
dc.description.abstract1. The pharmacology, biochemistry and structure-activity relationships pertinent to the D1 and D2 subtypes of dopamine receptors are reviewed. 2. Recent advances in receptor purification and our understanding of the secondary messenger systems involved are presented. 3. D1 and D2 receptors of central nervous, endocrine and peripheral systems are identical.en
dc.language.isoenen
dc.subject.otherAnimalsen
dc.subject.otherDopamine Agents.pharmacologyen
dc.subject.otherDrug Designen
dc.subject.otherHumansen
dc.subject.otherReceptors, Dopamine.drug effectsen
dc.titleDopamine receptors: classification, properties and drug development.en
dc.typeJournal Articleen
dc.identifier.journaltitleClinical and Experimental Pharmacology & Physiologyen
dc.identifier.affiliationUniversity of Melbourne, Clinical Pharmacology and Therapeutics Unit, Austin Hospital, Heidelberg, Victoria, Australiaen
dc.description.pages511-5en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/2569952en
dc.type.austinJournal Articleen
item.grantfulltextnone-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.openairetypeJournal Article-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
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