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Genomics|December 9, 2000
Cloning and characterization of human NTT5 and v7-3: two orphan transporters of the Na+/Cl- -dependent neurotransmitter transporter gene familyM K Farmer, M J Robbins, A D Medhurst, et al.British Journal of Pharmacology|March 1, 1996
Potentiation by 2,2'-pyridylisatogen tosylate of ATP-responses at a recombinant P2Y1 purinoceptorB F King, C Dacquet, A U Ziganshin, et al.Journal of Medicinal Chemistry|May 28, 1993
Synthesis and serotonergic activity of 5-(oxadiazolyl)tryptamines: potent agonists for 5-HT1D receptorsL J Street, R Baker, J L Castro, et al.The Journal of Pharmacology and Experimental Therapeutics|November 1, 1995
Functional correlates of dopamine D3 receptor activation in the rat in vivo and their modulation by the selective antagonist, (+)-S 14297: II. Both D2 and "silent" D3 autoreceptors control synthesis and release in mesolimbic, mesocortical and nigrostriatal pathwaysA Gobert, J M Rivet, V Audinot, et al.Journal of Medicinal Chemistry|March 1, 1990
Structure and activity of hydrogenated derivatives of (+)-5-methyl-10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5,10-imine (MK-801)T A Lyle, C A Magill, S F Britcher, et al.Neuropharmacology|August 26, 1998
Interaction of the anxiogenic agent, RS-30199, with 5-HT1A receptors: modulation of sexual activity in the male ratM Spedding, A Newman-Tancredi, M J Millan, et al.Journal of Medicinal Chemistry|February 1, 1990
Affinity of 2-(tetrahydroisoquinolin-2-ylmethyl)- and 2-(isoindolin-2-ylmethyl)imidazolines for alpha-adrenoceptors. Differential affinity of imidazolines for the [3H]idazoxan-labeled alpha 2-adrenoceptor vs the [3H]yohimbine-labeled siteR D Clark, J Berger, P Garg, et al.British Journal of Pharmacology|February 1, 1993
Modulation of central noradrenergic function by RS-15385-197W S Redfern, A C MacKinnon, C M Brown, et al.European Journal of Pharmacology|August 1, 1994
S 14297, a novel selective ligand at cloned human dopamine D3 receptors, blocks 7-OH-DPAT-induced hypothermia in ratsM J Millan, V Audinot, J M Rivet, et al.British Journal of Pharmacology|August 6, 2000
Characterization of SB-271046: a potent, selective and orally active 5-HT(6) receptor antagonistC Routledge, S M Bromidge, S F Moss, et al.Pageof 21