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D Kimball

Showing results (51-60 of 72) with videos related to

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International Journal for Parasitology|February 27, 1999
Influence of permethrin, diazinon and ivermectin treatments on insecticide resistance in the horn fly (Diptera: Muscidae)R L Byford, M E Craig, S M DeRouen, et al.
Current Pharmaceutical Biotechnology|May 24, 2014
BSA Au clusters as a probe for enhanced fluorescence detection using multipulse excitation schemeSangram L Raut, Ryan Rich, Rafal Fudala, et al.
The Journal of Antibiotics|March 1, 1986
New mitomycin analogs produced by directed biosynthesisC A Claridge, J A Bush, T W Doyle, et al.
Journal of Photochemistry and Photobiology. B, Biology|January 7, 2016
Photophysical characterization of anticancer drug valrubicin in rHDL nanoparticles and its use as an imaging agentSunil Shah, Rahul Chib, Sangram Raut, et al.
Journal of Medicinal Chemistry|August 21, 1992
Dihydropyrimidine calcium channel blockers. 4. Basic 3-substituted-4-aryl-1,4-dihydropyrimidine-5-carboxylic acid esters. Potent antihypertensive agentsG C Rovnyak, K S Atwal, A Hedberg, et al.
Biochemistry|March 14, 1995
Benzothiazepine binding domain of purified L-type calcium channels: direct labeling using a novel fluorescent diltiazem analogueT Brauns, Z W Cai, S D Kimball, et al.
Journal of Medicinal Chemistry|January 6, 1995
Calcium entry blockers and activators: conformational and structural determinants of dihydropyrimidine calcium channel modulatorsG C Rovnyak, S D Kimball, B Beyer, et al.
Physical Chemistry Chemical Physics : PCCP|January 23, 2016
A triazine-based BODIPY trimer as a molecular viscometerSangram L Raut, Joseph D Kimball, Rafal Fudala, et al.
Journal of Medicinal Chemistry|February 21, 1992
Benzazepinone calcium channel blockers. 4. Structure-activity overview and intracellular binding siteS D Kimball, D M Floyd, J Das, et al.
Journal of Medicinal Chemistry|July 10, 1992
Benzazepinone calcium channel blockers. 5. Effects on antihypertensive activity associated with N1 and aromatic substituentsJ Das, D M Floyd, S D Kimball, et al.
Pageof 8

Showing results (51-60 of 72) with videos related to

Sort By:
Pageof 8
International Journal for Parasitology|February 27, 1999
Influence of permethrin, diazinon and ivermectin treatments on insecticide resistance in the horn fly (Diptera: Muscidae)R L Byford, M E Craig, S M DeRouen, et al.
Current Pharmaceutical Biotechnology|May 24, 2014
BSA Au clusters as a probe for enhanced fluorescence detection using multipulse excitation schemeSangram L Raut, Ryan Rich, Rafal Fudala, et al.
The Journal of Antibiotics|March 1, 1986
New mitomycin analogs produced by directed biosynthesisC A Claridge, J A Bush, T W Doyle, et al.
Journal of Photochemistry and Photobiology. B, Biology|January 7, 2016
Photophysical characterization of anticancer drug valrubicin in rHDL nanoparticles and its use as an imaging agentSunil Shah, Rahul Chib, Sangram Raut, et al.
Journal of Medicinal Chemistry|August 21, 1992
Dihydropyrimidine calcium channel blockers. 4. Basic 3-substituted-4-aryl-1,4-dihydropyrimidine-5-carboxylic acid esters. Potent antihypertensive agentsG C Rovnyak, K S Atwal, A Hedberg, et al.
Biochemistry|March 14, 1995
Benzothiazepine binding domain of purified L-type calcium channels: direct labeling using a novel fluorescent diltiazem analogueT Brauns, Z W Cai, S D Kimball, et al.
Journal of Medicinal Chemistry|January 6, 1995
Calcium entry blockers and activators: conformational and structural determinants of dihydropyrimidine calcium channel modulatorsG C Rovnyak, S D Kimball, B Beyer, et al.
Physical Chemistry Chemical Physics : PCCP|January 23, 2016
A triazine-based BODIPY trimer as a molecular viscometerSangram L Raut, Joseph D Kimball, Rafal Fudala, et al.
Journal of Medicinal Chemistry|February 21, 1992
Benzazepinone calcium channel blockers. 4. Structure-activity overview and intracellular binding siteS D Kimball, D M Floyd, J Das, et al.
Journal of Medicinal Chemistry|July 10, 1992
Benzazepinone calcium channel blockers. 5. Effects on antihypertensive activity associated with N1 and aromatic substituentsJ Das, D M Floyd, S D Kimball, et al.
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