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Anti-Cancer Drug Design|April 15, 2000
The quinobenzoxazines: relationship between DNA binding and biological activityY Kwok, D Sun, J J Clement, et al.Biochemistry|August 17, 1993
Structure of the altromycin B (N7-guanine)-DNA adduct. A proposed prototypic DNA adduct structure for the pluramycin antitumor antibioticsD Sun, M Hansen, J J Clement, et al.The Journal of Biological Chemistry|November 26, 1998
Topoisomerase II site-directed alkylation of DNA by psorospermin and its effect on topoisomerase II-mediated DNA cleavageY Kwok, L H HurleyThe Journal of Biological Chemistry|June 8, 1999
Structural insight into a quinolone-topoisomerase II-DNA complex. Further evidence for a 2:2 quinobenzoxazine-mg2+ self-assembly model formed in the presence of topoisomerase iiY Kwok, Q Zeng, L H HurleyProceedings of the National Academy of Sciences of the United States of America|November 13, 1998
Topoisomerase II-mediated site-directed alkylation of DNA by psorospermin and its use in mapping other topoisomerase II poison binding sitesY Kwok, Q Zeng, L H HurleyBiochemistry|August 24, 2000
Efficient, Mg(2+)-dependent photochemical DNA cleavage by the antitumor quinobenzoxazine (S)-A-62176H Yu, Y Kwok, L H Hurley, et al.Journal of Medicinal Chemistry|May 15, 1992
Structure-activity relationships of (+)-CC-1065 analogues in the inhibition of helicase-catalyzed unwinding of duplex DNAD Sun, L H HurleyGene|November 4, 1994
Binding of Sp1 to the 21-bp repeat region of SV40 DNA: effect of intrinsic and drug-induced DNA bending between GC boxesD Sun, L H HurleyAnti-Cancer Drug Design|February 1, 1992
Inhibition of T4 DNA ligase activity by (+)-CC-1065: demonstration of the importance of the stiffening and winding effects of (+)-CC-1065 on DNAD Sun, L H HurleyChemistry & Biology|July 1, 1995
TBP binding to the TATA box induces a specific downstream unwinding site that is targeted by pluramycinD Sun, L H HurleyPageof 182