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D W Robertson

Showing results (31-40 of 88) with videos related to

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Journal of Medicinal Chemistry|May 1, 1987
Imidazole anticonvulsants: structure-activity relationships of [(biphenylyloxy)alkyl]imidazolesD W Robertson, E E Beedle, R Lawson, et al.
Journal of Medicinal Chemistry|February 1, 1982
Antiestrogen basicity--activity relationships: a comparison of the estrogen receptor binding and antiuterotrophic potencies of several analogues of (Z)-1,2-diphenyl-1-[4-[2-(dimethylamino)ethoxy]phenyl]-1-butene (tamoxifen, Nolvadex) having altered basicityD W Robertson, J A Katzenellenbogen, J R Hayes, et al.
Molecular Pharmacology|December 1, 1986
LY195115: a potent, selective inhibitor of cyclic nucleotide phosphodiesterase located in the sarcoplasmic reticulumR F Kauffman, V G Crowe, B G Utterback, et al.
Journal of Medicinal Chemistry|July 1, 1988
Absolute configurations and pharmacological activities of the optical isomers of fluoxetine, a selective serotonin-uptake inhibitorD W Robertson, J H Krushinski, R W Fuller, et al.
Brain Research|July 5, 1991
Localization of 5-HT3 receptors in the rat brain using [3H]LY278584D R Gehlert, S L Gackenheimer, D T Wong, et al.
The Journal of Biological Chemistry|March 25, 1981
Interaction of a high affinity anti-estrogen (alpha-[4-pyrrolidinoethoxy]phenyl-4-hydroxy-alpha'-nitrostilbene, CI628M) with uterine estrogen receptorsB S Katzenellenbogen, E J Pavlik, D W Robertson, et al.
Journal of Medicinal Chemistry|July 1, 1989
Synthesis of a tritium-labeled indolidan analogue and its use as a radioligand for phosphodiesterase-inhibitor cardiotonic binding sitesD W Robertson, J H Krushinski, B G Utterback, et al.
Neuropharmacology|October 1, 1992
Comparison of norfluoxetine enantiomers as serotonin uptake inhibitors in vivoR W Fuller, H D Snoddy, J H Krushinski, et al.
The Journal of Pharmacology and Experimental Therapeutics|April 1, 1992
LY215840, a potent 5-hydroxytryptamine (5-HT)2 receptor antagonist, blocks vascular and platelet 5-HT2 receptors and delays occlusion in a rabbit model of thrombosisM L Cohen, D W Robertson, W E Bloomquist, 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.
Pageof 9

Showing results (31-40 of 88) with videos related to

Sort By:
Pageof 9
Journal of Medicinal Chemistry|May 1, 1987
Imidazole anticonvulsants: structure-activity relationships of [(biphenylyloxy)alkyl]imidazolesD W Robertson, E E Beedle, R Lawson, et al.
Journal of Medicinal Chemistry|February 1, 1982
Antiestrogen basicity--activity relationships: a comparison of the estrogen receptor binding and antiuterotrophic potencies of several analogues of (Z)-1,2-diphenyl-1-[4-[2-(dimethylamino)ethoxy]phenyl]-1-butene (tamoxifen, Nolvadex) having altered basicityD W Robertson, J A Katzenellenbogen, J R Hayes, et al.
Molecular Pharmacology|December 1, 1986
LY195115: a potent, selective inhibitor of cyclic nucleotide phosphodiesterase located in the sarcoplasmic reticulumR F Kauffman, V G Crowe, B G Utterback, et al.
Journal of Medicinal Chemistry|July 1, 1988
Absolute configurations and pharmacological activities of the optical isomers of fluoxetine, a selective serotonin-uptake inhibitorD W Robertson, J H Krushinski, R W Fuller, et al.
Brain Research|July 5, 1991
Localization of 5-HT3 receptors in the rat brain using [3H]LY278584D R Gehlert, S L Gackenheimer, D T Wong, et al.
The Journal of Biological Chemistry|March 25, 1981
Interaction of a high affinity anti-estrogen (alpha-[4-pyrrolidinoethoxy]phenyl-4-hydroxy-alpha'-nitrostilbene, CI628M) with uterine estrogen receptorsB S Katzenellenbogen, E J Pavlik, D W Robertson, et al.
Journal of Medicinal Chemistry|July 1, 1989
Synthesis of a tritium-labeled indolidan analogue and its use as a radioligand for phosphodiesterase-inhibitor cardiotonic binding sitesD W Robertson, J H Krushinski, B G Utterback, et al.
Neuropharmacology|October 1, 1992
Comparison of norfluoxetine enantiomers as serotonin uptake inhibitors in vivoR W Fuller, H D Snoddy, J H Krushinski, et al.
The Journal of Pharmacology and Experimental Therapeutics|April 1, 1992
LY215840, a potent 5-hydroxytryptamine (5-HT)2 receptor antagonist, blocks vascular and platelet 5-HT2 receptors and delays occlusion in a rabbit model of thrombosisM L Cohen, D W Robertson, W E Bloomquist, 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.
Pageof 9