Sequence-Specific Targeting of Duplex DNA Using a Camptothecin-Triple Helix Forming Oligonucleotide Conjugate and Topoisomerase I
- 1 July 1997
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 119 (29) , 6939-6940
- https://doi.org/10.1021/ja9702475
Abstract
No abstract availableThis publication has 18 references indexed in Scilit:
- X-ray lenses near realityNature, 1996
- Sequence‐Specific Recognition of DNA by a Major and Minor Groove Binding LigandAngewandte Chemie International Edition in English, 1996
- Antisense Sequence-Directed Cross-Linking of DNA Oligonucleotides by Mitomycin CBioconjugate Chemistry, 1996
- The Current Status of Camptothecin Analogues as Antitumor AgentsJNCI Journal of the National Cancer Institute, 1993
- A kinetic and Mechanistic Study of the Hydrolysis of Camptothecin and Some AnaloguesJournal of Pharmaceutical Sciences, 1992
- New technique for uncoupling the cleavage and religation reactions of Eukaryotic Topoisomerase I.Journal of Molecular Biology, 1991
- Synthesis of water-soluble (aminoalkyl)camptothecin analogs: inhibition of topoisomerase I and antitumor activityJournal of Medicinal Chemistry, 1991
- On the mechanism of topoisomerase I inhibition by camptothecin: evidence for binding to an enzyme-DNA complexBiochemistry, 1989
- Complementary addressed modification of double‐stranded DNA within a ternary complexFEBS Letters, 1988
- Sequence-Specific Cleavage of Double Helical DNA by Triple Helix FormationScience, 1987