نتایج جستجو برای: beta agonists

تعداد نتایج: 220167  

Journal: :Journal of clinical pathology 1989
D H Pamphilon R J Boon A G Prentice A Rozkovec

Propranolol, a non-selective beta blocker, was administered orally in therapeutic doses. The effects of a single dose (160 mg) and one week's treatment (80 mg twice a day) on platelet function were compared in healthy young subjects. There were no significant changes in circulating platelet aggregates, template bleeding time, platelet factor 3 availability and thromboxane beta 2 (TX beta 2) gen...

Journal: :The Journal of experimental biology 1980
E Marder D Paupardin-Tritsch

A pharmacological analysis was made of the depolarizing acetylcholine (ACh) response found on the gastric mill I muscles of the crabs Cancer pagurus, Cancer irroratus and Cancer borealis. Acetylcholine, carbamylcholine, trimethylammonium, nicotine, and dimethyl-4-phenyl-piperazinium were effective in producing contractures and depolarizations in these muscles. No response to decamethonium, sube...

Journal: :The Journal of pharmacology and experimental therapeutics 1998
M I Damaj M Fei-Yin M Dukat W Glassco R A Glennon B R Martin

The objective of this study was to determine which nicotinic receptor subtypes are involved in antinociception and their site of action. For that, the antinociceptive effects of several nicotinic receptor ligands were evaluated in the tail-flick test both after s.c. and intrathecal (i.t.) administration. Nicotine and other nicotine agonists increased tail-flick latencies in a dose-dependent man...

Journal: :Clinical infectious diseases : an official publication of the Infectious Diseases Society of America 1997
F Moosdeen

The expression of resistance to cephalosporins is highly varied and due to various mechanisms. The greatest disadvantage of the cephalosporins is that they are inactivated by the array of beta-lactamases produced by bacteria. The high levels of chromosomal enzymes produced by these organisms are a major cause of cephalosporin resistance. Plasmid-mediated beta-lactamases (PMBLs) have also been i...

Journal: :Journal of biomolecular screening 2002
Yu-Xin Yan Deborah M Boldt-Houle Bonnie P Tillotson Melissa A Gee Brian J D'Eon Xiao-Jia Chang Corinne E M Olesen Michelle A J Palmer

A novel cell-based functional assay to directly monitor G protein-coupled receptor (GPCR) activation in a high-throughput format, based on a common GPCR regulation mechanism, the interaction between beta-arrestin and ligand-activated GPCR, is described. A protein-protein interaction technology, the InteraX trade mark system, uses a pair of inactive beta-galactosidase (beta-gal) deletion mutants...

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