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D W Bonhaus

Showing results (41-50 of 61) with videos related to

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British Journal of Pharmacology|June 1, 1995
The pharmacology and distribution of human 5-hydroxytryptamine2B (5-HT2B) receptor gene products: comparison with 5-HT2A and 5-HT2C receptorsD W Bonhaus, C Bach, A DeSouza, et al.
The Journal of Pharmacology and Experimental Therapeutics|March 1, 1995
Characterization of the electrophysiological, biochemical and behavioral actions of epibatidineD W Bonhaus, K R Bley, C A Broka, et al.
Journal of Neurochemistry|August 1, 1994
Cloning and expression of a 5-hydroxytryptamine7 receptor positively coupled to adenylyl cyclaseA P Tsou, A Kosaka, C Bach, et al.
British Journal of Pharmacology|February 1, 1995
The interaction of RS 25259-197, a potent and selective antagonist, with 5-HT3 receptors, in vitroE H Wong, R Clark, E Leung, et al.
British Journal of Pharmacology|September 1, 1993
RS 23597-190: a potent and selective 5-HT4 receptor antagonistR M Eglen, K Bley, D W Bonhaus, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 1, 1991
Increased AMPA-sensitive quisqualate receptor binding and reduced NMDA receptor binding in epileptic human hippocampusD A Hosford, B J Crain, Z Cao, et al.
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.
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.
Pageof 7

Showing results (41-50 of 61) with videos related to

Sort By:
Pageof 7
British Journal of Pharmacology|June 1, 1995
The pharmacology and distribution of human 5-hydroxytryptamine2B (5-HT2B) receptor gene products: comparison with 5-HT2A and 5-HT2C receptorsD W Bonhaus, C Bach, A DeSouza, et al.
The Journal of Pharmacology and Experimental Therapeutics|March 1, 1995
Characterization of the electrophysiological, biochemical and behavioral actions of epibatidineD W Bonhaus, K R Bley, C A Broka, et al.
Journal of Neurochemistry|August 1, 1994
Cloning and expression of a 5-hydroxytryptamine7 receptor positively coupled to adenylyl cyclaseA P Tsou, A Kosaka, C Bach, et al.
British Journal of Pharmacology|February 1, 1995
The interaction of RS 25259-197, a potent and selective antagonist, with 5-HT3 receptors, in vitroE H Wong, R Clark, E Leung, et al.
British Journal of Pharmacology|September 1, 1993
RS 23597-190: a potent and selective 5-HT4 receptor antagonistR M Eglen, K Bley, D W Bonhaus, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 1, 1991
Increased AMPA-sensitive quisqualate receptor binding and reduced NMDA receptor binding in epileptic human hippocampusD A Hosford, B J Crain, Z Cao, et al.
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.
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.
Pageof 7