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British Journal of Pharmacology|August 6, 2000
Disparate ligand-mediated Ca(2+) responses by wild-type, mutant Ser(200)Ala and Ser(204)Ala alpha(2A)-adrenoceptor: G(alpha15) fusion proteins: evidence for multiple ligand-activation binding sitesP J Pauwels, F C ColpaertThe Journal of Pharmacology and Experimental Therapeutics|March 1, 1991
5-hydroxytryptamine (HT)1A receptors and the tail-flick response. II. High efficacy 5-HT1A agonists attenuate morphine-induced antinociception in mice in a competitive-like mannerM J Millan, F C ColpaertThe Journal of Pharmacology and Experimental Therapeutics|March 1, 1991
5-hydroxytryptamine (HT)1A receptors and the tail-flick response. III. Structurally diverse 5-HT1A partial agonists attenuate mu- but not kappa-opioid antinociception in mice and ratsM J Millan, F C ColpaertArchives Internationales De Pharmacodynamie Et De Therapie|September 1, 1975
On the narcotic cuing action of fentanyl and other narcotic analgesic drugsF C Colpaert, C J NiemegeersNeuropharmacology|February 1, 1995
The 5-HT1D receptor antagonist GR 127,935 is an agonist at cloned human 5-HT1D alpha receptor sitesP J Pauwels, F C ColpaertBiochemical Pharmacology|November 9, 1995
Differentiation between partial and silent 5-HT1D beta receptor antagonists using rat C6-glial and Chinese hamster ovary cell lines permanently transfected with a cloned human 5-HT1D beta receptor geneP J Pauwels, F C ColpaertThe Journal of Pharmacology and Experimental Therapeutics|July 1, 1984
Agonist and antagonist effects of prototype opiate drugs in rats discriminating fentanyl from saline: characteristics of partial generalizationF C Colpaert, P A JanssenNeuropharmacology|August 1, 1983
A characterization of LSD-antagonist effects of pirenperone in the ratF C Colpaert, P A JanssenEuropean Journal of Pharmacology|January 1, 1975
Narcotic withdrawal like mouse jumping produced by amphetamine and L-DOPAH Lal, F C Colpaert, P LaduronEuropean Journal of Pharmacology|November 20, 1990
Binding of typical and atypical antipsychotics to 5-HT1C and 5-HT2 sites: clozapine potently interacts with 5-HT1C sitesH Canton, L Verrièle, F C ColpaertPageof 24