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	61.	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 cells. [electronic resource] by Bonhaus, D W Herman, R C Brown, C M Cao, Z Chang, L F Loury, D N Sze, P Zhang, L Hunter, J C Producer: 19970213 In: Neuropharmacology vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	62.	[3H]RS-23597-190, a potent 5-hydroxytryptamine4 antagonist labels sigma-1 but not sigma-2 binding sites in guinea pig brain. [electronic resource] by Bonhaus, D W Loury, D N Jakeman, L B Hsu, S A To, Z P Leung, E Zeitung, K D Eglen, R M Wong, E H Producer: 19941125 In: The Journal of pharmacology and experimental therapeutics vol. 271 Availability: No items available. Save to lists Add to cart (remove)
	63.	Enhanced delayed matching performance in younger and older macaques administered the 5-HT4 receptor agonist, RS 17017. [electronic resource] by Terry, A V Buccafusco, J J Jackson, W J Prendergast, M A Fontana, D J Wong, E H Bonhaus, D W Weller, P Eglen, R M Producer: 19980521 In: Psychopharmacology vol. 135 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	64.	(R) and (S) RS 56532: mixed 5-HT3 and 5-HT4 receptor ligands with opposing enantiomeric selectivity. [electronic resource] by Eglen, R M Bonhaus, D W Clark, R D Johnson, L G Lee, C H Leung, E Smith, W L Wong, E H Whiting, R L Producer: 19941230 In: Neuropharmacology vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	65.	Functional evidence equating the pharmacologically-defined alpha 1A- and cloned alpha 1C-adrenoceptor: studies in the isolated perfused kidney of rat. [electronic resource] by Blue, D R Bonhaus, D W Ford, A P Pfister, J R Sharif, N A Shieh, I A Vimont, R L Williams, T J Clarke, D E Producer: 19951018 In: British journal of pharmacology vol. 115 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	66.	Comparison of 5-HT4 receptors in guinea-pig colon and rat oesophagus: effects of novel agonists and antagonists. [electronic resource] by Leung, E Pulido-Rios, M T Bonhaus, D W Pekins, L A Zeitung, K D Hsu, S A Clark, R D Wong, E H Eglen, R M Producer: 19961219 In: Naunyn-Schmiedeberg's archives of pharmacology vol. 354 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	67.	Ligand efficacy and potency at recombinant alpha2 adrenergic receptors: agonist-mediated [35S]GTPgammaS binding. [electronic resource] by Jasper, J R Lesnick, J D Chang, L K Yamanishi, S S Chang, T K Hsu, S A Daunt, D A Bonhaus, D W Eglen, R M Producer: 19980608 In: Biochemical pharmacology vol. 55 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	68.	[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) receptors. [electronic resource] by Bonhaus, D W Berger, J Adham, N Branchek, T A Hsu, S A Loury, D N Leung, E Wong, E H Clark, R D Eglen, R M Producer: 19970915 In: Neuropharmacology vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	69.	Catecholamine modulatory effects of nepicastat (RS-25560-197), a novel, potent and selective inhibitor of dopamine-beta-hydroxylase. [electronic resource] by Stanley, W C Li, B Bonhaus, D W Johnson, L G Lee, K Porter, S Walker, K Martinez, G Eglen, R M Whiting, R L Hegde, S S Producer: 19980105 In: British journal of pharmacology vol. 121 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	70.	2-(Quinuclidin-3-yl)pyrido[4,3-b]indol-1-ones and isoquinolin-1-ones. Potent conformationally restricted 5-HT3 receptor antagonists. [electronic resource] by Clark, R D Miller, A B Berger, J Repke, D B Weinhardt, K K Kowalczyk, B A Eglen, R M Bonhaus, D W Lee, C H Michel, A D Producer: 19931029 In: Journal of medicinal chemistry vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	71.	RS-102221: a novel high affinity and selective, 5-HT2C receptor antagonist. [electronic resource] by Bonhaus, D W Weinhardt, K K Taylor, M DeSouza, A McNeeley, P M Szczepanski, K Fontana, D J Trinh, J Rocha, C L Dawson, M W Flippin, L A Eglen, R M Producer: 19970915 In: Neuropharmacology vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	72.	RS-127445: a selective, high affinity, orally bioavailable 5-HT2B receptor antagonist. [electronic resource] by Bonhaus, D W Flippin, L A Greenhouse, R J Jaime, S Rocha, C Dawson, M Van Natta, K Chang, L K Pulido-Rios, T Webber, A Leung, E Eglen, R M Martin, G R Producer: 19991005 In: British journal of pharmacology vol. 127 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	73.	RS-17053 (N-[2-(2-cyclopropylmethoxyphenoxy)ethyl]-5-chloro-alpha, alpha-dimethyl-1H-indole-3-ethanamine hydrochloride), a selective alpha 1A-adrenoceptor antagonist, displays low affinity for functional alpha 1-adrenoceptors in human prostate: implications for adrenoceptor classification. [electronic resource] by Ford, A P Arredondo, N F Blue, D R Bonhaus, D W Jasper, J Kava, M S Lesnick, J Pfister, J R Shieh, I A Vimont, R L Williams, T J McNeal, J E Stamey, T A Clarke, D E Producer: 19960703 In: Molecular pharmacology vol. 49 Availability: No items available. Save to lists Add to cart (remove)