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Drug Metabolism and Disposition: the Biological Fate of Chemicals|November 1, 1984
Reductive metabolism of furazolidone by Escherichia coli and rat liver in vitroR T Abraham, J E Knapp, M B Minnigh, et al.Cancer Chemotherapy and Pharmacology|January 1, 1994
Increased intracellular Ca2+ signaling caused by the antitumor agent helenalin and its analoguesG Powis, A Gallegos, R T Abraham, et al.Bioorganic & Medicinal Chemistry|March 18, 2000
Steroidal derived acids as inhibitors of human Cdc25A protein phosphataseH Peng, W Xie, D I Kim, et al.Genes & Development|December 15, 2000
Functional interactions between BRCA1 and the checkpoint kinase ATR during genotoxic stressR S Tibbetts, D Cortez, K M Brumbaugh, et al.Mayo Clinic Proceedings|December 1, 1996
Cyclosporine in the treatment of dermatologic disease: an updateK K Lim, W P Su, A L Schroeter, et al.Progress in Cell Cycle Research|January 1, 1995
Mechanism of action of rapamycin: new insights into the regulation of G1-phase progression in eukaryotic cellsG J Wiederrecht, C J Sabers, G J Brunn, et al.The Journal of Experimental Medicine|December 31, 1997
Regulation of ZAP-70 intracellular localization: visualization with the green fluorescent proteinJ Sloan-Lancaster, W Zhang, J Presley, et al.Cancer Research|July 26, 2000
A direct linkage between the phosphoinositide 3-kinase-AKT signaling pathway and the mammalian target of rapamycin in mitogen-stimulated and transformed cellsA Sekulić, C C Hudson, J L Homme, et al.Cancer Research|September 15, 1999
Inhibition of ATM and ATR kinase activities by the radiosensitizing agent, caffeineJ N Sarkaria, E C Busby, R S Tibbetts, et al.Molecular and Cellular Biology|March 6, 1998
Genetic evidence for differential coupling of Syk family kinases to the T-cell receptor: reconstitution studies in a ZAP-70-deficient Jurkat T-cell lineB L Williams, K L Schreiber, W Zhang, et al.Pageof 11