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European Journal of Pharmacology|July 23, 1991
Tedisamil (KC 8857) differentially inhibits the 86Rb+ efflux-stimulating and vasorelaxant properties of cromakalimK Bray, U QuastNaunyn-Schmiedeberg'S Archives of Pharmacology|October 1, 1996
Binding of [3H]-P1075, an opener of ATP-sensitive K+ channels, to rat glomerular preparationsF Metzger, U QuastBiochimica Et Biophysica Acta|January 15, 1981
Soybean trypsin inhibitor (Kunitz) is doubleheaded. Kinetics of the interaction of alpha-chymotrypsin with each sideB Bösterling, U QuastStrahlentherapie|May 1, 1978
New individual tissue compensators for high-energetic photons. Part I. Principle and procedureU Quast, K KrauseNaunyn-Schmiedeberg'S Archives of Pharmacology|February 1, 1992
Differential inhibition by tedisamil (KC 8857) and glibenclamide of the responses to cromakalim and minoxidil sulphate in rat isolated aortaK Bray, U QuastEuropean Journal of Pharmacology|August 6, 1991
Cromakalim inhibits contractions of the rat isolated mesenteric bed induced by noradrenaline but not caffeine in Ca(2+)-free medium: evidence for interference with receptor-mediated Ca2+ mobilizationU Quast, Y BaumlinNaunyn-Schmiedeberg'S Archives of Pharmacology|September 1, 1988
Comparison of the effluxes of 42K+ and 86Rb+ elicited by cromakalim (BRL 34915) in tonic and phasic vascular tissueU Quast, Y BaumlinBiochemical Pharmacology|September 1, 1982
Interaction of [3H]flunitrazepam with the benzodiazepine receptor: evidence for a ligand-induced conformation changeU Quast, H MählmannNaunyn-Schmiedeberg'S Archives of Pharmacology|September 28, 1998
Interaction of the diuretics torasemide and U-37883A with the K(ATP) channel in rat isolated aortaC Löffler-Walz, U QuastEuropean Journal of Pharmacology|April 15, 1993
The individual enantiomers of cis-cromakalim possess K+ channel opening activityU Quast, E B VillhauerPageof 15