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Journal of Medicinal Chemistry|January 22, 1998
Strategies for rapid deconvolution of combinational libraries: comparative evaluation using a model systemD A Konings, J R Wyatt, D J Ecker, et al.Nucleic Acids Research|April 25, 1993
Rational screening of oligonucleotide combinatorial libraries for drug discoveryD J Ecker, T A Vickers, R Hanecak, et al.Journal of Medicinal Chemistry|July 5, 1996
Deconvolution of combinatorial libraries for Drug discovery: theoretical comparison of pooling strategiesD A Konings, J R Wyatt, D J Ecker, et al.Molecular Pharmacology|August 1, 1987
SKF 104353, a high affinity antagonist for human and guinea pig lung leukotriene D4 receptor, blocked phosphatidylinositol metabolism and thromboxane synthesis induced by leukotriene D4S Mong, H L Wu, J Miller, et al.Cancer Research|January 1, 1985
Evaluation of the in vivo antitumor activity and in vitro cytotoxic properties of auranofin, a coordinated gold compound, in murine tumor modelsC K Mirabelli, R K Johnson, C M Sung, et al.The Biochemical Journal|July 1, 1989
Solubilization of rat liver vasopressin receptors as a complex with a guanine-nucleotide-binding protein and phosphoinositide-specific phospholipase CN Aiyar, C F Bennett, P Nambi, et al.Biochemical Pharmacology|November 1, 1986
Evidence for tyrosine at the ligand binding center of beta-adrenergic receptorsR G Shorr, M D Minnich, L Gotlib, et al.Journal of Medicinal Chemistry|January 20, 1995
Deconvolution of combinatorial libraries for drug discovery: a model systemS M Freier, D A Konings, J R Wyatt, et al.Bioorganic & Medicinal Chemistry|May 1, 1996
'Mutational SURF': a strategy for improving lead compounds identified from combinatorial librariesS M Freier, D A Konings, J R Wyatt, et al.Molecular Pharmacology|March 1, 1987
A novel radiolabeled vasopressin antagonist: [3H-Phe]-desGlyd(CH2)5D-Tyr(Et)VAVP, [3H]-SK&F 101926F L Stassen, G Heckman, D Schmidt, et al.Pageof 27