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Biochemistry|December 11, 1990
Interaction of a macrocyclic bisacridine with DNAJ M Veal, Y Li, S C Zimmerman, et al.Nucleic Acids Research|September 25, 1990
Crystal and solution structures of the oligonucleotide d(ATGCGCAT)2: a combined X-ray and NMR studyG R Clark, D G Brown, M R Sanderson, et al.Journal of Medicinal Chemistry|November 24, 1995
Design and synthesis of conformationally constrained analogues of 4-(3-butoxy-4-methoxybenzyl)imidazolidin-2-one (Ro 20-1724) as potent inhibitors of cAMP-specific phosphodiesteraseM F Brackeen, D J Cowan, J A Stafford, et al.Bioorganic & Medicinal Chemistry Letters|March 4, 2000
The discovery of potent cRaf1 kinase inhibitorsK Lackey, M Cory, R Davis, et al.Journal of Medicinal Chemistry|December 1, 2001
Oxindole-based inhibitors of cyclin-dependent kinase 2 (CDK2): design, synthesis, enzymatic activities, and X-ray crystallographic analysisH N Bramson, J Corona, S T Davis, et al.Science (New York, N.Y.)|January 6, 2001
Prevention of chemotherapy-induced alopecia in rats by CDK inhibitorsS T Davis, B G Benson, H N Bramson, et al.Pageof 2