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Assay and Drug Development Technologies|July 3, 2008
A robust and high-capacity [(35)S]GTPgammaS binding assay for determining antagonist and inverse agonist pharmacological parameters of histamine H(3) receptor ligandsThomas R Miller, John L Baranowski, Brian R Estvander, et al.The Journal of Pharmacology and Experimental Therapeutics|September 15, 2007
An 80-amino acid deletion in the third intracellular loop of a naturally occurring human histamine H3 isoform confers pharmacological differences and constitutive activityGerold Bongers, Kathleen M Krueger, Thomas R Miller, et al.Journal of Neuroscience Methods|July 5, 2011
KCNQ2/3 openers show differential selectivity and site of action across multiple KCNQ channelsDi Zhang, Rama Thimmapaya, Xu-Feng Zhang, et al.Biochemical Pharmacology|August 6, 2004
Pharmacological and behavioral properties of A-349821, a selective and potent human histamine H3 receptor antagonistTimothy A Esbenshade, Gerard B Fox, Kathleen M Krueger, et al.British Journal of Pharmacology|May 6, 2009
In vitro and in vivo characterization of A-940894: a potent histamine H4 receptor antagonist with anti-inflammatory propertiesM I Strakhova, C A Cuff, A M Manelli, et al.Biochemical Pharmacology|March 21, 2007
Novel heterocyclic-substituted benzofuran histamine H3 receptor antagonists: in vitro properties, drug-likeness, and behavioral activityMarlon Cowart, Gregory A Gfesser, Kaitlin E Browman, et al.Chemical Biology & Drug Design|June 22, 2007
From bacterial genomes to novel antibacterial agents: discovery, characterization, and antibacterial activity of compounds that bind to HI0065 (YjeE) from Haemophilus influenzaeClaude G Lerner, Philip J Hajduk, Rolf Wagner, et al.Pageof 4