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D E Mais

Showing results (41-50 of 77) with videos related to

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The Journal of Pharmacology and Experimental Therapeutics|December 1, 1985
Binding of a thromboxane A2/prostaglandin H2 receptor antagonist to washed human plateletsD E Mais, R M Burch, D L Saussy, et al.
Biochemical Pharmacology|February 15, 1988
Subcellular localization of a thromboxane A2/prostaglandin H2 receptor antagonist binding site in human plateletsD L Saussy, D E Mais, D A Baron, et al.
The Journal of Pharmacology and Experimental Therapeutics|August 11, 1992
7-[(1R,2S,3S,5R)-6,6-dimethyl-3-(4- iodobenzenesulfonylamino)bicyclo[3.1.1]hept-2-yl]-5(Z)-heptenoic acid: a novel high-affinity radiolabeled antagonist for platelet thromboxane A2/prostaglandin H2 receptorsM Naka, D E Mais, T A Morinelli, et al.
Bioorganic & Medicinal Chemistry Letters|January 5, 1999
Development of dual-acting agents for thromboxane receptor antagonism and thromboxane synthase inhibition. 2. Design, synthesis, and evaluation of a novel series of phenyl oxazole derivativesK Takeuchi, T J Kohn, D E Mais, et al.
Circulation|January 1, 1990
Increased platelet thromboxane A2/prostaglandin H2 receptors in patients with acute myocardial infarctionG W Dorn, N Liel, J L Trask, et al.
The Journal of Biological Chemistry|August 26, 1998
Expression, characterization, and purification of C-terminally hexahistidine-tagged thromboxane A2 receptorsS Pawate, K L Schey, G P Meier, et al.
Neurochemistry International|October 1, 1993
Synthesis and evaluation of [125I]-(S)-iodozacopride, a high affinity radioligand for 5HT3 receptorsD R Gehlert, D A Schober, S L Gackenheimer, et al.
Journal of Medicinal Chemistry|February 17, 1998
5-Aryl-1,2-dihydro-5H-chromeno[3,4-f]quinolines as potent, orally active, nonsteroidal progesterone receptor agonists: the effect of D-ring substituentsJ P Edwards, S J West, K B Marschke, et al.
The Journal of Biological Chemistry|August 25, 1986
Alpha 1-adrenergic stimulation of arachidonic acid release and metabolism in a rat thyroid cell line. Mediation of cell replication by prostaglandin E2R M Burch, A Luini, D E Mais, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 1, 1989
Difluorothromboxane A2 and stereoisomers: stable derivatives of thromboxane A2 with differential effects on platelets and blood vesselsT A Morinelli, A K Okwu, D E Mais, et al.
Pageof 8

Showing results (41-50 of 77) with videos related to

Sort By:
Pageof 8
The Journal of Pharmacology and Experimental Therapeutics|December 1, 1985
Binding of a thromboxane A2/prostaglandin H2 receptor antagonist to washed human plateletsD E Mais, R M Burch, D L Saussy, et al.
Biochemical Pharmacology|February 15, 1988
Subcellular localization of a thromboxane A2/prostaglandin H2 receptor antagonist binding site in human plateletsD L Saussy, D E Mais, D A Baron, et al.
The Journal of Pharmacology and Experimental Therapeutics|August 11, 1992
7-[(1R,2S,3S,5R)-6,6-dimethyl-3-(4- iodobenzenesulfonylamino)bicyclo[3.1.1]hept-2-yl]-5(Z)-heptenoic acid: a novel high-affinity radiolabeled antagonist for platelet thromboxane A2/prostaglandin H2 receptorsM Naka, D E Mais, T A Morinelli, et al.
Bioorganic & Medicinal Chemistry Letters|January 5, 1999
Development of dual-acting agents for thromboxane receptor antagonism and thromboxane synthase inhibition. 2. Design, synthesis, and evaluation of a novel series of phenyl oxazole derivativesK Takeuchi, T J Kohn, D E Mais, et al.
Circulation|January 1, 1990
Increased platelet thromboxane A2/prostaglandin H2 receptors in patients with acute myocardial infarctionG W Dorn, N Liel, J L Trask, et al.
The Journal of Biological Chemistry|August 26, 1998
Expression, characterization, and purification of C-terminally hexahistidine-tagged thromboxane A2 receptorsS Pawate, K L Schey, G P Meier, et al.
Neurochemistry International|October 1, 1993
Synthesis and evaluation of [125I]-(S)-iodozacopride, a high affinity radioligand for 5HT3 receptorsD R Gehlert, D A Schober, S L Gackenheimer, et al.
Journal of Medicinal Chemistry|February 17, 1998
5-Aryl-1,2-dihydro-5H-chromeno[3,4-f]quinolines as potent, orally active, nonsteroidal progesterone receptor agonists: the effect of D-ring substituentsJ P Edwards, S J West, K B Marschke, et al.
The Journal of Biological Chemistry|August 25, 1986
Alpha 1-adrenergic stimulation of arachidonic acid release and metabolism in a rat thyroid cell line. Mediation of cell replication by prostaglandin E2R M Burch, A Luini, D E Mais, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 1, 1989
Difluorothromboxane A2 and stereoisomers: stable derivatives of thromboxane A2 with differential effects on platelets and blood vesselsT A Morinelli, A K Okwu, D E Mais, et al.
Pageof 8