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D E Mais

Showing results (31-40 of 77) with videos related to

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Biochemical and Biophysical Research Communications|November 15, 1985
Hydrodynamic properties of a thromboxane A2/prostaglandin H2 antagonist binding site solubilized from human plateletsR M Burch, D E Mais, S H Pepkowitz, et al.
The Journal of Pharmacology and Experimental Therapeutics|May 1, 1991
Quantitative autoradiography of the binding sites for [125I] iodoglyburide, a novel high-affinity ligand for ATP-sensitive potassium channels in rat brainD R Gehlert, S L Gackenheimer, D E Mais, et al.
Journal of Medicinal Chemistry|April 23, 1999
5-Aryl-1,2,3,4-tetrahydrochromeno[3,4-f]quinolin-3-ones as a novel class of nonsteroidal progesterone receptor agonists: effect of A-ring modificationL Zhi, C M Tegley, K B Marschke, et al.
Biochemical and Biophysical Research Communications|October 15, 1986
Photoaffinity labelling of a thromboxane A2/prostaglandin H2 antagonist binding site in human plateletsD E Mais, R M Burch, J E Oatis, et al.
Biochimica Et Biophysica Acta|July 11, 1989
Photoaffinity labelling of the human platelet thromboxane A2/prostaglandin H2 receptorD E Mais, C Yoakim, Y Guindon, et al.
Life Sciences|January 1, 1990
Characterization of thromboxane A2/prostaglandin H2 receptors in human vascular smooth muscle cellsT A Morinelli, D E Mais, J E Oatis, et al.
Eicosanoids|January 11, 1992
Binding of a novel radioiodinated thromboxane A2/prostaglandin H2 antagonist to guinea pig lung membranesD L Saussy, P D Clark, D L Gunn, et al.
Biochemical Pharmacology|June 15, 1987
Decrease in agonist affinity for human platelet thromboxane A2/prostaglandin H2 receptors induced by a platelet-derived supernatantG W Dorn, R M Burch, P J Kochel, et al.
The Journal of Endocrinology|May 1, 1995
Anti-progesterone antibody administration and the impairment of postpartum maternal care in miceM W Wang, D L Crombie, D E Mais, et al.
Molecular and Cellular Biology|December 1, 1994
The A and B isoforms of the human progesterone receptor operate through distinct signaling pathways within target cellsD X Wen, Y F Xu, D E Mais, et al.
Pageof 8

Showing results (31-40 of 77) with videos related to

Sort By:
Pageof 8
Biochemical and Biophysical Research Communications|November 15, 1985
Hydrodynamic properties of a thromboxane A2/prostaglandin H2 antagonist binding site solubilized from human plateletsR M Burch, D E Mais, S H Pepkowitz, et al.
The Journal of Pharmacology and Experimental Therapeutics|May 1, 1991
Quantitative autoradiography of the binding sites for [125I] iodoglyburide, a novel high-affinity ligand for ATP-sensitive potassium channels in rat brainD R Gehlert, S L Gackenheimer, D E Mais, et al.
Journal of Medicinal Chemistry|April 23, 1999
5-Aryl-1,2,3,4-tetrahydrochromeno[3,4-f]quinolin-3-ones as a novel class of nonsteroidal progesterone receptor agonists: effect of A-ring modificationL Zhi, C M Tegley, K B Marschke, et al.
Biochemical and Biophysical Research Communications|October 15, 1986
Photoaffinity labelling of a thromboxane A2/prostaglandin H2 antagonist binding site in human plateletsD E Mais, R M Burch, J E Oatis, et al.
Biochimica Et Biophysica Acta|July 11, 1989
Photoaffinity labelling of the human platelet thromboxane A2/prostaglandin H2 receptorD E Mais, C Yoakim, Y Guindon, et al.
Life Sciences|January 1, 1990
Characterization of thromboxane A2/prostaglandin H2 receptors in human vascular smooth muscle cellsT A Morinelli, D E Mais, J E Oatis, et al.
Eicosanoids|January 11, 1992
Binding of a novel radioiodinated thromboxane A2/prostaglandin H2 antagonist to guinea pig lung membranesD L Saussy, P D Clark, D L Gunn, et al.
Biochemical Pharmacology|June 15, 1987
Decrease in agonist affinity for human platelet thromboxane A2/prostaglandin H2 receptors induced by a platelet-derived supernatantG W Dorn, R M Burch, P J Kochel, et al.
The Journal of Endocrinology|May 1, 1995
Anti-progesterone antibody administration and the impairment of postpartum maternal care in miceM W Wang, D L Crombie, D E Mais, et al.
Molecular and Cellular Biology|December 1, 1994
The A and B isoforms of the human progesterone receptor operate through distinct signaling pathways within target cellsD X Wen, Y F Xu, D E Mais, et al.
Pageof 8