S-(+)-aporphines are not selective for human D3 dopamine receptors
- 1 April 1994
- journal article
- Published by Springer Nature in Cellular and Molecular Neurobiology
- Vol. 14 (2) , 185-191
- https://doi.org/10.1007/bf02090784
Abstract
No abstract availableKeywords
This publication has 20 references indexed in Scilit:
- Hexahydrobenzo[a]phenanthridines: novel dopamine D3 receptor ligandsEuropean Journal of Pharmacology, 1993
- Isomeric selectivity at dopamine D3 receptorsEuropean Journal of Pharmacology, 1993
- Synthesis of (.+-.)-2'-trans-7-hydroxy-2-[N-(3'-iodo-2'-propenyl)-N-n-propylamino]tetralin (trans-7-OH-PIPAT): a new D3 dopamine receptor ligandJournal of Medicinal Chemistry, 1993
- Differential Visualization of Dopamine D2 and D3 Receptor Sites in Rat Brain. A Comparative Study Using In Situ Hybridization Histochemistry and Ligand Binding AutoradiographyEuropean Journal of Neuroscience, 1993
- Stable expression of human D3 dopamine receptors in GH4C1 pituitary cellsFEBS Letters, 1992
- Antagonism of limbic and extrapyramidal actions of intracerebrally injected dopamine by ergolines with partial D2 agonist activity in the ratBrain Research, 1992
- Pharmacology of human dopamine D3 receptor expressed in a mammalian cell line: comparison with D2 receptorEuropean Journal of Pharmacology: Molecular Pharmacology, 1992
- Localization of dopamine D3 receptor mRNA in the rat brain using in situ hybridization histochemistry: comparison with dopamine D2 receptor mRNABrain Research, 1991
- Molecular cloning and characterization of a novel dopamine receptor (D3) as a target for neurolepticsNature, 1990
- Multiple receptors for dopamineNature, 1979