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Molecular Pharmacology|July 1, 1995
Serotonergic antagonists differentially inhibit spontaneous activity and decrease ligand binding capacity of the rat 5-hydroxytryptamine type 2C receptor in Sf9 cellsJ Labrecque, A Fargin, M Bouvier, et al.
Molecular Pharmacology|March 1, 1994
Inverse agonist activity of beta-adrenergic antagonistsP Chidiac, T E Hebert, M Valiquette, et al.
Biochemistry|June 17, 1997
Cardiac muscarinic receptors. Cooperativity as the basis for multiple states of affinityP Chidiac, M A Green, A B Pawagi, et al.
Endocrinology|September 21, 2001
Calcitonin (CT) rapidly increases NA(+)/H(+) exchange and metabolic acid production: effects mediated selectively by the C1A CT receptor isoformA Santhanagopal, P Chidiac, W C Horne, et al.
The Journal of Clinical Endocrinology and Metabolism|August 15, 2001
Stimulation of human extravillous trophoblast migration by IGF-II is mediated by IGF type 2 receptor involving inhibitory G protein(s) and phosphorylation of MAPKT McKinnon, C Chakraborty, L M Gleeson, et al.
European Journal of Pharmacology|May 12, 1997
Influence of receptor density on the patterns of beta2-adrenocepter desensitizationG Rousseau, N Guilbault, A Da Silva, et al.
Molecular Pharmacology|September 22, 2000
RGS3 is a GTPase-activating protein for g(ialpha) and g(qalpha) and a potent inhibitor of signaling by GTPase-deficient forms of g(qalpha) and g(11alpha)A Scheschonka, C W Dessauer, S Sinnarajah, et al.
Australian and New Zealand Journal of Medicine|October 1, 1978
Radionuclide quantitation of left-to-right cardiac shunts in childrenB M McIlveen, R Höschl, I P Murray, et al.
The Journal of Biological Chemistry|December 18, 1998
The N-terminal domain of RGS4 confers receptor-selective inhibition of G protein signalingW Zeng, X Xu, S Popov, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|September 16, 1998
Dynamic regulation of RGS2 suggests a novel mechanism in G-protein signaling and neuronal plasticityT Ingi, A M Krumins, P Chidiac, et al.
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