Showing results (171-180 of 201) with videos related to

Sort By:
Pageof 21
Physical Review. E|August 20, 2024
Hexagonal vortices enable faster colloidal crystal grain coarseningHelen K Chaffee, Eric Corona-Oceguera, Chris G Couto, et al.
Journal of Medicinal Chemistry|April 14, 1995
Discovery and structure-activity relationships of sulfonamide ETA-selective antagonistsP D Stein, D M Floyd, S Bisaha, et al.
Emerging Infectious Diseases|December 19, 2001
A unique Mycobacterium species isolated from an epizootic of striped bass (Morone saxatilis)M W Rhodes, H Kator, S Kotob, et al.
International Journal of Systematic and Evolutionary Microbiology|April 12, 2000
Mycobacterium septicum sp. nov., a new rapidly growing species associated with catheter-related bacteraemiaM F Schinsky, M M McNeil, A M Whitney, et al.
Prevention Science : the Official Journal of the Society for Prevention Research|April 10, 2018
Marijuana Promotion Online: an Investigation of Dispensary PracticesPatricia A Cavazos-Rehg, Melissa J Krauss, Elizabeth Cahn, 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.
Bioorganic & Medicinal Chemistry|October 1, 1993
1-Benzazepin-2-one calcium channel blockers--VI. Receptor-binding model and possible relationship to desmethoxyverapamilS D Kimball, J T Hunt, J C Barrish, et al.
Journal of Medicinal Chemistry|September 1, 1990
Dihydropyrimidine calcium channel blockers. 2. 3-substituted-4-aryl-1,4-dihydro-6-methyl-5-pyrimidinecarboxylic acid esters as potent mimics of dihydropyridinesK S Atwal, G C Rovnyak, S D Kimball, et al.
Journal of Medicinal Chemistry|February 21, 1992
Benzazepinone calcium channel blockers. 2. Structure-activity and drug metabolism studies leading to potent antihypertensive agents. Comparison with benzothiazepinonesD M Floyd, S D Kimball, J Krapcho, et al.
Pageof 21