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The Journal of Pharmacology and Experimental Therapeutics|December 1, 1995
Pharmacological evaluation of 1229U91, a novel high-affinity and selective neuropeptide Y-Y1 receptor antagonistS S Hegde, D W Bonhaus, W Stanley, et al.
Neuropharmacology|May 1, 1996
The beta 1 sodium channel subunit modifies the interactions of neurotoxins and local anesthetics with the rat brain IIA alpha sodium channel in isolated membranes but not in intact cellsD W Bonhaus, R C Herman, C M Brown, et al.
Toxicon : Official Journal of the International Society on Toxinology|August 1, 1995
The sea anemone purine, caissarone: adenosine receptor antagonismR A Cooper, J C de Freitas, F Porreca, et al.
Journal of Computer-Aided Molecular Design|March 29, 2002
High-affinity interactions of ligands at recombinant guinea pig 5HT7 receptorsR E Wilcox, J E Ragan, R S Pearlman, et al.
Neuropharmacology|March 1, 1994
(R) and (S) RS 56532: mixed 5-HT3 and 5-HT4 receptor ligands with opposing enantiomeric selectivityR M Eglen, D W Bonhaus, R D Clark, et al.
Psychopharmacology|April 16, 1998
Enhanced delayed matching performance in younger and older macaques administered the 5-HT4 receptor agonist, RS 17017A V Terry, J J Buccafusco, W J Jackson, et al.
The Journal of Pharmacology and Experimental Therapeutics|October 1, 1994
[3H]RS-23597-190, a potent 5-hydroxytryptamine4 antagonist labels sigma-1 but not sigma-2 binding sites in guinea pig brainD W Bonhaus, D N Loury, L B Jakeman, et al.
Biochemical Pharmacology|May 30, 1998
Ligand efficacy and potency at recombinant alpha2 adrenergic receptors: agonist-mediated [35S]GTPgammaS bindingJ R Jasper, J D Lesnick, L K Chang, et al.
Naunyn-Schmiedeberg'S Archives of Pharmacology|July 1, 1996
Comparison of 5-HT4 receptors in guinea-pig colon and rat oesophagus: effects of novel agonists and antagonistsE Leung, M T Pulido-Rios, D W Bonhaus, et al.
Neuropharmacology|April 1, 1997
[3H]RS 57639, a high affinity, selective 5-HT4 receptor partial agonist, specifically labels guinea-pig striatal and rat cloned (5-HT4S and 5-HT4L) receptorsD W Bonhaus, J Berger, N Adham, et al.
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