Identification of Topoisomerase I Mutations Affecting Both DNA Cleavage and Interaction with Camptothecin a
暂无分享,去创建一个
D. Kufe | P. Haluska | Y. Hsiang | E. Rubin | A. Bharti | Xi-guang Li
[1] D. Hall,et al. Detailed analysis of the basic domain of the E2F1 transcription factor indicates that it is unique among bHLH proteins. , 1994, Oncogene.
[2] D. Kufe,et al. Identification of a mutant human topoisomerase I with intact catalytic activity and resistance to 9-nitro-camptothecin. , 1994, The Journal of biological chemistry.
[3] O. Westergaard,et al. Characterization of intra- and intermolecular DNA ligation mediated by eukaryotic topoisomerase I. Role of bipartite DNA interaction in the ligation process. , 1994, The Journal of biological chemistry.
[4] S. Shuman,et al. Requirements for noncovalent binding of vaccinia topoisomerase I to duplex DNA. , 1994, Nucleic acids research.
[5] Y. Pommier,et al. Cloning of Chinese hamster DNA topoisomerase I cDNA and identification of a single point mutation responsible for camptothecin resistance. , 1993, The Journal of biological chemistry.
[6] J. Wang,et al. Camptothecin resistance from a single mutation changing glycine 363 of human DNA topoisomerase I to cysteine. , 1993, Cancer research.
[7] B. Gatto,et al. DNA minor groove-binding ligands: a different class of mammalian DNA topoisomerase I inhibitors. , 1993, Proceedings of the National Academy of Sciences of the United States of America.
[8] P. Traktman,et al. Biochemical analysis of mutant alleles of the vaccinia virus topoisomerase I carrying targeted substitutions in a highly conserved domain. , 1993, The Journal of biological chemistry.
[9] A. Andersen,et al. Eukaryotic topoisomerase I-mediated cleavage requires bipartite DNA interaction. Cleavage of DNA substrates containing strand interruptions implicates a role for topoisomerase I in illegitimate recombination. , 1993, The Journal of biological chemistry.
[10] A. Bodley,et al. A new mammalian DNA topoisomerase I poison Hoechst 33342: cytotoxicity and drug resistance in human cell cultures. , 1993, Cancer research.
[11] E K Rowinsky,et al. The current status of camptothecin analogues as antitumor agents. , 1993, Journal of the National Cancer Institute.
[12] J. Alsner,et al. Characterization of an altered DNA catalysis of a camptothecin-resistant eukaryotic topoisomerase I. , 1993, Nucleic acids research.
[13] J. Alsner,et al. Camptothecin inhibits both the cleavage and religation reactions of eukaryotic DNA topoisomerase I. , 1992, Journal of molecular biology.
[14] N. Saijo,et al. Detection of topoisomerase I gene point mutation in CPT-11 resistant lung cancer cell line. , 1992, Biochemical and biophysical research communications.
[15] S. Shuman,et al. Covalent and noncovalent DNA binding by mutants of vaccinia DNA topoisomerase I. , 1992, The Journal of biological chemistry.
[16] Peggy J. Farnham,et al. Expression cloning of a cDNA encoding a retinoblastoma-binding protein with E2F-like properties , 1992, Cell.
[17] J. Svejstrup,et al. New technique for uncoupling the cleavage and religation reactions of eukaryotic topoisomerase I. The mode of action of camptothecin at a specific recognition site. , 1991, Journal of molecular biology.
[18] S. Shuman. Site-specific interaction of vaccinia virus topoisomerase I with duplex DNA. Minimal DNA substrate for strand cleavage in vitro. , 1991, The Journal of biological chemistry.
[19] J. Wang,et al. DNA topoisomerases: why so many? , 1991, The Journal of biological chemistry.
[20] N. Osheroff,et al. Eukaryotic topoisomerases recognize nucleic acid topology by preferentially interacting with DNA crossovers. , 1990, The EMBO journal.
[21] R. Hertzberg,et al. Irreversible trapping of the DNA-topoisomerase I covalent complex. Affinity labeling of the camptothecin binding site. , 1990, The Journal of biological chemistry.
[22] M. Nissen,et al. The A.T-DNA-binding domain of mammalian high mobility group I chromosomal proteins. A novel peptide motif for recognizing DNA structure. , 1990, The Journal of biological chemistry.
[23] L. Liu,et al. Arrest of replication forks by drug-stabilized topoisomerase I-DNA cleavable complexes as a mechanism of cell killing by camptothecin. , 1989, Cancer research.
[24] R. Sternglanz,et al. Mapping of the active site tyrosine of eukaryotic DNA topoisomerase I. , 1989, The Journal of biological chemistry.
[25] M. McHugh,et al. Effect of minor groove binding drugs on mammalian topoisomerase I activity. , 1989, Biochemical pharmacology.
[26] R. Hertzberg,et al. On the mechanism of topoisomerase I inhibition by camptothecin: evidence for binding to an enzyme-DNA complex. , 1989, Biochemistry.
[27] E. Di Mauro,et al. Regulation of the function of eukaryotic DNA topoisomerase I: topological conditions for inactivity. , 1989, Proceedings of the National Academy of Sciences of the United States of America.
[28] K. Kohn,et al. Topoisomerase I interaction with SV40 DNA in the presence and absence of camptothecin. , 1988, Nucleic acids research.
[29] L. Bolund,et al. Sequence-dependent effect of camptothecin on human topoisomerase I DNA cleavage. , 1988, Journal of molecular biology.
[30] L. Liu,et al. Identification of mammalian DNA topoisomerase I as an intracellular target of the anticancer drug camptothecin. , 1988, Cancer research.
[31] Y. Suzuki,et al. Characterization of a mammalian mutant with a camptothecin-resistant DNA topoisomerase I. , 1987, Proceedings of the National Academy of Sciences of the United States of America.
[32] R. Burgess,et al. Nucleotide sequence preference at rat liver and wheat germ type 1 DNA topoisomerase breakage sites in duplex SV40 DNA. , 1984, Nucleic acids research.
[33] L. Liu,et al. Recognition sites of eukaryotic DNA topoisomerase I: DNA nucleotide sequencing analysis of topo I cleavage sites on SV40 DNA. , 1982, Nucleic acids research.
[34] J. Champoux,et al. The effect of salt on the binding of the eucaryotic DNA nicking-closing enzyme to DNA and chromatin. , 1981, Biochimica et biophysica acta.