-
1
-
-
0034923502
-
DNA topoisomerases: Structure, function, and mechanism
-
Champoux,J.J. (2001) DNA topoisomerases: Structure, function, and mechanism. Annu. Rev. Biochem, 70, 369-413.
-
(2001)
Annu. Rev. Biochem
, vol.70
, pp. 369-413
-
-
Champoux, J.J.1
-
2
-
-
0036085460
-
Cellular roles of DNA topoisomerases: A molecular perspective
-
Wang,J.C. (2002) Cellular roles of DNA topoisomerases: A molecular perspective. Nature Rev. Mol. Cell. Biol, 3, 430-440.
-
(2002)
Nature Rev. Mol. Cell. Biol
, vol.3
, pp. 430-440
-
-
Wang, J.C.1
-
3
-
-
0030014783
-
DNA topoisomerases
-
Wang,J.C. (1996) DNA topoisomerases. Annu. Rev. Biochem, 65, 635-692.
-
(1996)
Annu. Rev. Biochem
, vol.65
, pp. 635-692
-
-
Wang, J.C.1
-
4
-
-
0032190561
-
Mechanism of action of eukaryotic topoisomerase II and drugs targeted to the enzyme
-
Burden,D.A. and Osheroff,N. (1998) Mechanism of action of eukaryotic topoisomerase II and drugs targeted to the enzyme. Biochim. Biophys. Acta, 1400, 139-154.
-
(1998)
Biochim. Biophys. Acta
, vol.1400
, pp. 139-154
-
-
Burden, D.A.1
Osheroff, N.2
-
5
-
-
0032189945
-
DNA sequence selectivity of topoisomerases and topoisomerase poisons
-
Capranico,G. and Binaschi,M. (1998) DNA sequence selectivity of topoisomerases and topoisomerase poisons. Biochim. Biophys. Acta, 1400, 185-194.
-
(1998)
Biochim. Biophys. Acta
, vol.1400
, pp. 185-194
-
-
Capranico, G.1
Binaschi, M.2
-
6
-
-
3142662140
-
Development of DNA topoisomerase-related therapeutics: A short perspective of new challenges
-
Capranico,G., Zagotto,G. and Palumbo,M. (2004) Development of DNA topoisomerase-related therapeutics: A short perspective of new challenges. Curr. Med. Chem. Anti-Canc. Agents, 4, 335-345.
-
(2004)
Curr. Med. Chem. Anti-Canc. Agents
, vol.4
, pp. 335-345
-
-
Capranico, G.1
Zagotto, G.2
Palumbo, M.3
-
7
-
-
0032168167
-
Etoposide: Four decades of development of a topoisomerase II inhibitor
-
Hande,K.R. (1998) Etoposide: Four decades of development of a topoisomerase II inhibitor. Eur. J. Cancer, 34, 1514-1521.
-
(1998)
Eur. J. Cancer
, vol.34
, pp. 1514-1521
-
-
Hande, K.R.1
-
9
-
-
22144473328
-
Etoposide, topoisomerase II and cancer
-
Baldwin,E.L. and Osheroff,N. (2005) Etoposide, topoisomerase II and cancer. Curr. Med. Chem. Anti-Canc. Agents, 5, 363-372.
-
(2005)
Curr. Med. Chem. Anti-Canc. Agents
, vol.5
, pp. 363-372
-
-
Baldwin, E.L.1
Osheroff, N.2
-
10
-
-
0032189262
-
Cell death induced by topoisomerase-targeted drugs: More questions than answers
-
Kaufmann,S.H. (1998) Cell death induced by topoisomerase-targeted drugs: more questions than answers. Biochim. Biophys. Acta, 1400, 195-211.
-
(1998)
Biochim. Biophys. Acta
, vol.1400
, pp. 195-211
-
-
Kaufmann, S.H.1
-
11
-
-
0037868272
-
Apoptosis induced by topoisomerase inhibitors
-
Sordet,O., Khan,Q.A., Kohn,K.W. and Pommier,Y. (2003) Apoptosis induced by topoisomerase inhibitors. Curr. Med. Chem. Anti-Canc. Agents, 3, 271-290.
-
(2003)
Curr. Med. Chem. Anti-Canc. Agents
, vol.3
, pp. 271-290
-
-
Sordet, O.1
Khan, Q.A.2
Kohn, K.W.3
Pommier, Y.4
-
12
-
-
0032189081
-
Secondary leukemias induced by topoisomerase-targeted drugs
-
Felix,C.A. (1998) Secondary leukemias induced by topoisomerase-targeted drugs. Biochim. Biophys. Acta, 1400, 233-255.
-
(1998)
Biochim. Biophys. Acta
, vol.1400
, pp. 233-255
-
-
Felix, C.A.1
-
13
-
-
0035859820
-
Near-precise interchromosomal recombination and functional DNA topoisomerase II cleavage sites at MLL and AF-4 genomic breakpoints in treatment-related acute lymphoblastic leukemia with t(4;11) translocation
-
Lovett,B.D., Lo Nigro,L., Rappaport,E.F., Blair,I.A., Osheroff,N., Zheng,N., Megonigal,M.D., Williams,W.R., Nowell,P.C. and Felix,C.A. (2001) Near-precise interchromosomal recombination and functional DNA topoisomerase II cleavage sites at MLL and AF-4 genomic breakpoints in treatment-related acute lymphoblastic leukemia with t(4;11) translocation. Proc. Natl Acad. Sci. USA, 98, 9802-9807.
-
(2001)
Proc. Natl Acad. Sci. USA
, vol.98
, pp. 9802-9807
-
-
Lovett, B.D.1
Lo Nigro, L.2
Rappaport, E.F.3
Blair, I.A.4
Osheroff, N.5
Zheng, N.6
Megonigal, M.D.7
Williams, W.R.8
Nowell, P.C.9
Felix, C.A.10
-
14
-
-
0035814808
-
Etoposide metabolites enhance DNA topoisomerase II cleavage near leukemia-associated MLL translocation breakpoints
-
Lovett,B.D., Strumberg,D., Blair,I.A., Pang,S., Burden,D.A., Megonigal,M.D., Rappaport,E.F., Rebbeck,T.R., Osheroff,N., Pommier,Y.G. et al. (2001) Etoposide metabolites enhance DNA topoisomerase II cleavage near leukemia-associated MLL translocation breakpoints. Biochemistry, 40, 1159-1170.
-
(2001)
Biochemistry
, vol.40
, pp. 1159-1170
-
-
Lovett, B.D.1
Strumberg, D.2
Blair, I.A.3
Pang, S.4
Burden, D.A.5
Megonigal, M.D.6
Rappaport, E.F.7
Rebbeck, T.R.8
Osheroff, N.9
Pommier, Y.G.10
-
15
-
-
0346753588
-
Reciprocal DNA topoisomerase II cleavage events at 50′-TATTA-3′ sequences in MLL and AF-9 create homologous single-stranded overhangs that anneal to form der(11) and der(9) genomic breakpoint junctions in treatment-related AML without further processing
-
Whitmarsh,R.J., Saginario,C., Zhuo,Y., Hilgenfeld,E., Rappaport,E.F., Megonigal,M.D., Carroll,M., Liu,M., Osheroff,N., Cheung,N.K. et al. (2003) Reciprocal DNA topoisomerase II cleavage events at 50′-TATTA-3′ sequences in MLL and AF-9 create homologous single-stranded overhangs that anneal to form der(11) and der(9) genomic breakpoint junctions in treatment-related AML without further processing. Oncogene, 22, 8448-8459.
-
(2003)
Oncogene
, vol.22
, pp. 8448-8459
-
-
Whitmarsh, R.J.1
Saginario, C.2
Zhuo, Y.3
Hilgenfeld, E.4
Rappaport, E.F.5
Megonigal, M.D.6
Carroll, M.7
Liu, M.8
Osheroff, N.9
Cheung, N.K.10
-
16
-
-
0030878687
-
Sequence-specific targeting of duplex DNA using a camptothecin-triple helix forming oligonucleotide conjugate and topoisomerase I
-
Matteucci,M., Lin,K.-Y., Huang,T., Wagner,R., Sternbach,D.D., Mehrotra,M. and Besterman,J.M. (1997) Sequence-specific targeting of duplex DNA using a camptothecin-triple helix forming oligonucleotide conjugate and topoisomerase I. J. Am. Chem. Soc, 119, 6939-6940.
-
(1997)
J. Am. Chem. Soc
, vol.119
, pp. 6939-6940
-
-
Matteucci, M.1
Lin, K.-Y.2
Huang, T.3
Wagner, R.4
Sternbach, D.D.5
Mehrotra, M.6
Besterman, J.M.7
-
17
-
-
0033303826
-
Targeting topoisomerase I cleavage to specific sequences of DNA by triple helix-forming oligonucleotide conjugates. A comparison between a rebeccamycin derivative and camptothecin
-
Arimondo,P.B., Bailly,C., Boutorine,A., Sun,J.S., Garestier,T. and Hélène,C. (1999) Targeting topoisomerase I cleavage to specific sequences of DNA by triple helix-forming oligonucleotide conjugates. A comparison between a rebeccamycin derivative and camptothecin. C R Acad. Sci. III, 322, 785-790.
-
(1999)
C R Acad. Sci. III
, vol.322
, pp. 785-790
-
-
Arimondo, P.B.1
Bailly, C.2
Boutorine, A.3
Sun, J.S.4
Garestier, T.5
Hélène, C.6
-
18
-
-
0036479132
-
Design and optimization of camptothecin conjugates of triple helix-forming oligonucleotides for sequence-specific DNA cleavage by topoisomerase I
-
Arimondo,P.B., Boutorine,A., Baldeyrou,B., Bailly,C., Kuwahara,M., Hecht,S.M., Sun,J.S., Garestier,T. and Hélène,C. (2002) Design and optimization of camptothecin conjugates of triple helix-forming oligonucleotides for sequence-specific DNA cleavage by topoisomerase I. J. Biol. Chem, 277, 3132-3140.
-
(2002)
J. Biol. Chem
, vol.277
, pp. 3132-3140
-
-
Arimondo, P.B.1
Boutorine, A.2
Baldeyrou, B.3
Bailly, C.4
Kuwahara, M.5
Hecht, S.M.6
Sun, J.S.7
Garestier, T.8
Hélène, C.9
-
19
-
-
4444358344
-
Camptothecins and topoisomerase I: A foot in the door. Targeting the genome beyond topoisomerase I with camptothecins and novel anticancer drugs: Importance of DNA replication, repair and cell cycle checkpoints
-
Pommier,Y. (2004) Camptothecins and topoisomerase I: A foot in the door. Targeting the genome beyond topoisomerase I with camptothecins and novel anticancer drugs: Importance of DNA replication, repair and cell cycle checkpoints. Curr. Med. Chem. Anti-Canc. Agents, 4, 429-434.
-
(2004)
Curr. Med. Chem. Anti-Canc. Agents
, vol.4
, pp. 429-434
-
-
Pommier, Y.1
-
20
-
-
0033736149
-
Linkage of a triple helix-forming oligonucleotide to amsacrine-4-carboxamide derivatives modulates the sequence-selectivity of topoisomerase II-mediated DNA cleavage
-
Arimondo,P., Bailly,C., Boutorine,A., Asseline,U., Sun,J.S., Garestier,T. and Hélène,C. (2000) Linkage of a triple helix-forming oligonucleotide to amsacrine-4-carboxamide derivatives modulates the sequence-selectivity of topoisomerase II-mediated DNA cleavage. Nucleosides Nucleotides Nucleic Acids, 19, 1205-1218.
-
(2000)
Nucleosides Nucleotides Nucleic Acids
, vol.19
, pp. 1205-1218
-
-
Arimondo, P.1
Bailly, C.2
Boutorine, A.3
Asseline, U.4
Sun, J.S.5
Garestier, T.6
Hélène, C.7
-
21
-
-
11144353698
-
Synthesis and biological activity of sulfonamide derivatives of epipodophyllotoxin
-
Guianvarc'h,D., Duca,M., Boukarim,C., Kraus-Berthier,L., Leonce,S., Pierre,A., Pfeiffer,B., Renard,P., Arimondo,P.B., Monneret,C. et al. (2004) Synthesis and biological activity of sulfonamide derivatives of epipodophyllotoxin. J. Med. Chem, 47, 2365-2374.
-
(2004)
J. Med. Chem
, vol.47
, pp. 2365-2374
-
-
Guianvarc'h, D.1
Duca, M.2
Boukarim, C.3
Kraus-Berthier, L.4
Leonce, S.5
Pierre, A.6
Pfeiffer, B.7
Renard, P.8
Arimondo, P.B.9
Monneret, C.10
-
22
-
-
19944430141
-
Synthesis and biological study of a new series of 4′-demethylepipodophyllotoxin derivatives
-
Duca,M., Guianvarc'h,D., Meresse,P., Bertounesque,E., Dauzonne,D., Kraus-Berthier,L., Thirot,S., Leonce,S., Pierre,A., Pfeiffer,B. et al. (2005) Synthesis and biological study of a new series of 4′-demethylepipodophyllotoxin derivatives. J. Med. Chem, 48, 593-603.
-
(2005)
J. Med. Chem
, vol.48
, pp. 593-603
-
-
Duca, M.1
Guianvarc'h, D.2
Meresse, P.3
Bertounesque, E.4
Dauzonne, D.5
Kraus-Berthier, L.6
Thirot, S.7
Leonce, S.8
Pierre, A.9
Pfeiffer, B.10
-
23
-
-
22644434395
-
Triple helix-forming oligonucleotides conjugated to new inhibitors of topoisomerase II: Synthesis and binding properties
-
Duca,M., Oussedik,K., Ceccaldi,A., Halby,L., Guianvarc'h,D., Dauzonne,D., Monneret,C., Sun,J.S. and Arimondo,P.B. (2005) Triple helix-forming oligonucleotides conjugated to new inhibitors of topoisomerase II: Synthesis and binding properties. Bioconjug Chem, 16, 873-884.
-
(2005)
Bioconjug Chem
, vol.16
, pp. 873-884
-
-
Duca, M.1
Oussedik, K.2
Ceccaldi, A.3
Halby, L.4
Guianvarc'h, D.5
Dauzonne, D.6
Monneret, C.7
Sun, J.S.8
Arimondo, P.B.9
-
24
-
-
0037470042
-
A two-drug model for etoposide action against human topoisomerase IIalpha
-
Bromberg,K.D., Burgin,A.B. and Osheroff,N. (2003) A two-drug model for etoposide action against human topoisomerase IIalpha. J. Biol. Chem, 278, 7406-7412.
-
(2003)
J. Biol. Chem
, vol.278
, pp. 7406-7412
-
-
Bromberg, K.D.1
Burgin, A.B.2
Osheroff, N.3
-
25
-
-
33751499160
-
Synthesis of a tetrafluoro-substituted aryl azide and its protio analogue as photoaffinity labeling reagents for the estrogen receptor
-
Pinney,K.G. and Katzenellenbogen,J.A. (1991) Synthesis of a tetrafluoro-substituted aryl azide and its protio analogue as photoaffinity labeling reagents for the estrogen receptor. J. Org. Chem., 56, 3125-3133.
-
(1991)
J. Org. Chem.
, vol.56
, pp. 3125-3133
-
-
Pinney, K.G.1
Katzenellenbogen, J.A.2
-
26
-
-
0014725117
-
Oligonucleotides interactions III. Circular dichroism studies of the conformation of deoxyoligonucleotides
-
Cantor,C.R., Warshaw,M.M. and Shapiro,H. (1970) Oligonucleotides interactions III. Circular dichroism studies of the conformation of deoxyoligonucleotides. Biopolymers, 9, 1059-1077.
-
(1970)
Biopolymers
, vol.9
, pp. 1059-1077
-
-
Cantor, C.R.1
Warshaw, M.M.2
Shapiro, H.3
-
27
-
-
0034502384
-
Rapid routes of synthesis of oligonucleotide conjugates from non-protected oligonucleotides and ligands possessing different nucleophilic or electrophilic functional groups
-
Grimm,G.N., Boutorine,A.S. and Hélène,C. (2000) Rapid routes of synthesis of oligonucleotide conjugates from non-protected oligonucleotides and ligands possessing different nucleophilic or electrophilic functional groups. Nucleosides Nucleotides Nucleic Acids, 19, 1943-1965.
-
(2000)
Nucleosides Nucleotides Nucleic Acids
, vol.19
, pp. 1943-1965
-
-
Grimm, G.N.1
Boutorine, A.S.2
Hélène, C.3
-
28
-
-
0034434229
-
Design of two etoposide-amsacrine conjugates: Topoisomerase II and tubuline polymerization inhibition and relation to cytotoxicity
-
Arimondo,P., Boukarim,C., Bailly,C., Dauzonne,D. and Monneret,C. (2000) Design of two etoposide-amsacrine conjugates: Topoisomerase II and tubuline polymerization inhibition and relation to cytotoxicity. Anticancer Drug Des, 15, 413-421.
-
(2000)
Anticancer Drug Des
, vol.15
, pp. 413-421
-
-
Arimondo, P.1
Boukarim, C.2
Bailly, C.3
Dauzonne, D.4
Monneret, C.5
-
29
-
-
0027418105
-
Oligonucleotides derived from 5-(1-propynyl)-2′-O- allyl-uridine and 5-(1-propynyl)-2′-O-allyl-cytidine: Synthesis and RNA duplex formation
-
Froehler,B.C., Jones,R.J., Cao,X.D. and Terhorst,T.J. (1993) Oligonucleotides derived from 5-(1-propynyl)-2′-O- allyl-uridine and 5-(1-propynyl)-2′-O-allyl-cytidine: Synthesis and RNA duplex formation. Tetrahedron Lett., 34, 1003-1006.
-
(1993)
Tetrahedron Lett.
, vol.34
, pp. 1003-1006
-
-
Froehler, B.C.1
Jones, R.J.2
Cao, X.D.3
Terhorst, T.J.4
-
30
-
-
0032971841
-
Triplex formation by oligonucleotides containing 5-(1-propynyl) -2′- deoxyuridine: Decreased magnesium dependence and improved intracellular gene targeting
-
Lacroix,L., Lacoste,J., Reddoch,J.F., Mergny,J.L., Levy,D.D., Seidman,M.M., Matteucci,M.D. and Glazer,P.M. (1999) Triplex formation by oligonucleotides containing 5-(1-propynyl)-2′-deoxyuridine: Decreased magnesium dependence and improved intracellular gene targeting. Biochemistry, 38, 1893-1901.
-
(1999)
Biochemistry
, vol.38
, pp. 1893-1901
-
-
Lacroix, L.1
Lacoste, J.2
Reddoch, J.F.3
Mergny, J.L.4
Levy, D.D.5
Seidman, M.M.6
Matteucci, M.D.7
Glazer, P.M.8
-
31
-
-
0034066219
-
Recognition and cleavage of DNA by rebeccamycin- or benzopyridoquinoxaline conjugated of triple helix-forming oligonucleotides
-
Arimondo,P.B., Moreau,P., Boutorine,A., Bailly,C., Prudhomme,M., Sun,J.S., Garestier,T. and Hélène,C. (2000) Recognition and cleavage of DNA by rebeccamycin- or benzopyridoquinoxaline conjugated of triple helix-forming oligonucleotides. Bioorg. Med. Chem, 8, 777-784.
-
(2000)
Bioorg. Med. Chem
, vol.8
, pp. 777-784
-
-
Arimondo, P.B.1
Moreau, P.2
Boutorine, A.3
Bailly, C.4
Prudhomme, M.5
Sun, J.S.6
Garestier, T.7
Hélène, C.8
-
32
-
-
0024849694
-
Nuclease protection by Drosophila DNA topoisomerase II. Enzyme/DNA contacts at the strong topoisomerase II cleavage sites
-
Lee,M.P., Sander,M. and Hsieh,T. (1989) Nuclease protection by Drosophila DNA topoisomerase II. Enzyme/DNA contacts at the strong topoisomerase II cleavage sites. J. Biol. Chem, 264, 21779-21787.
-
(1989)
J. Biol. Chem
, vol.264
, pp. 21779-21787
-
-
Lee, M.P.1
Sander, M.2
Hsieh, T.3
-
33
-
-
0025056628
-
Eukaryotic topoisomerase II preferentially cleaves alternating purine-pyrimidine repeats
-
Spitzner,J.R., Chung,I.K. and Muller,M.T. (1990) Eukaryotic topoisomerase II preferentially cleaves alternating purine-pyrimidine repeats. Nucleic Acids Res, 18, 1-11.
-
(1990)
Nucleic Acids Res
, vol.18
, pp. 1-11
-
-
Spitzner, J.R.1
Chung, I.K.2
Muller, M.T.3
-
34
-
-
0025119181
-
Characterization of the interaction between topoisomerase II and DNA by transcriptional footprinting
-
Thomsen,B., Bendixen,C., Lund,K., Andersen,A.H., Sorensen,B.S. and Westergaard,O. (1990) Characterization of the interaction between topoisomerase II and DNA by transcriptional footprinting. J. Mol. Biol, 215, 237-244.
-
(1990)
J. Mol. Biol
, vol.215
, pp. 237-244
-
-
Thomsen, B.1
Bendixen, C.2
Lund, K.3
Andersen, A.H.4
Sorensen, B.S.5
Westergaard, O.6
-
35
-
-
0032557571
-
Mapping drug interactions at the covalent topoisomerase II-DNA complex by bisantrene/amsacrine congeners
-
Capranico,G., Guano,F., Moro,S., Zagotto,G., Sissi,C., Gatto,B., Zunino,F., Menta,E. and Palumbo,M.(1998) Mapping drug interactions at the covalent topoisomerase II-DNA complex by bisantrene/amsacrine congeners. J. Biol. Chem, 273, 12732-12739.
-
(1998)
J. Biol. Chem
, vol.273
, pp. 12732-12739
-
-
Capranico, G.1
Guano, F.2
Moro, S.3
Zagotto, G.4
Sissi, C.5
Gatto, B.6
Zunino, F.7
Menta, E.8
Palumbo, M.9
-
36
-
-
0028007482
-
Localization of an aminoacridine antitumor agent in a type II topoisomerase-DNA complex
-
Freudenreich,C.H. and Kreuzer,K.N. (1994) Localization of an aminoacridine antitumor agent in a type II topoisomerase-DNA complex. Proc. Natl Acad. Sci. USA, 91, 11007-11011.
-
(1994)
Proc. Natl Acad. Sci. USA
, vol.91
, pp. 11007-11011
-
-
Freudenreich, C.H.1
Kreuzer, K.N.2
-
37
-
-
0000385944
-
Design of new anti-cancer agents based on topoisomerase poisons targeted to specific DNA sequences
-
Arimondo,P.B. and Hélène,C. (2001) Design of new anti-cancer agents based on topoisomerase poisons targeted to specific DNA sequences. Curr. Med. Chem. Anti-Canc. Agents, 1, 219-235.
-
(2001)
Curr. Med. Chem. Anti-Canc. Agents
, vol.1
, pp. 219-235
-
-
Arimondo, P.B.1
Hélène, C.2
-
38
-
-
0242317688
-
Spatial organization of topoisomerase I-mediated DNA cleavage induced by camptothecin-oligonucleotide conjugates
-
Arimondo,P.B., Angenault,S., Halby,L., Boutorine,A., Schmidt,F., Monneret,C., Garestier,T., Sun,J.S., Bailly,C. and Hélène,C. (2003) Spatial organization of topoisomerase I-mediated DNA cleavage induced by camptothecin-oligonucleotide conjugates. Nucleic Acids Res, 31, 4031-4040.
-
(2003)
Nucleic Acids Res
, vol.31
, pp. 4031-4040
-
-
Arimondo, P.B.1
Angenault, S.2
Halby, L.3
Boutorine, A.4
Schmidt, F.5
Monneret, C.6
Garestier, T.7
Sun, J.S.8
Bailly, C.9
Hélène, C.10
-
39
-
-
0034637574
-
Assignment of functional amino acids around the active site of human DNA topoisomerase IIalpha
-
Okada,Y., Ito,Y., Kikuchi,A., Nimura,Y., Yoshida,S. and Suzuki,M. (2000) Assignment of functional amino acids around the active site of human DNA topoisomerase IIalpha. J. Biol. Chem, 275, 24630-24638.
-
(2000)
J. Biol. Chem
, vol.275
, pp. 24630-24638
-
-
Okada, Y.1
Ito, Y.2
Kikuchi, A.3
Nimura, Y.4
Yoshida, S.5
Suzuki, M.6
-
40
-
-
0033214044
-
Molecular analysis of yeast and human type II topoisomerases. Enzyme-DNA and drug interactions
-
Strumberg,D., Nitiss,J.L., Dong,J., Kohn,K.W. and Pommier,Y. (1999) Molecular analysis of yeast and human type II topoisomerases. Enzyme-DNA and drug interactions. J. Biol. Chem, 274, 28246-28255.
-
(1999)
J. Biol. Chem
, vol.274
, pp. 28246-28255
-
-
Strumberg, D.1
Nitiss, J.L.2
Dong, J.3
Kohn, K.W.4
Pommier, Y.5
-
41
-
-
0035852792
-
Analysis of etoposide binding to subdomains of human DNA topoisomerase II alpha in the absence of DNA
-
Leroy,D., Kajava,A.V., Frei,C. and Gasser,S.M. (2001) Analysis of etoposide binding to subdomains of human DNA topoisomerase II alpha in the absence of DNA. Biochemistry, 40, 1624-1634.
-
(2001)
Biochemistry
, vol.40
, pp. 1624-1634
-
-
Leroy, D.1
Kajava, A.V.2
Frei, C.3
Gasser, S.M.4
-
42
-
-
9644295787
-
A mutation in Escherichia coli DNA gyrase conferring quinolone resistance results in sensitivity to drugs targeting eukaryotic topoisomerase II
-
Gruger,T., Nitiss,J.L., Maxwell,A., Zechiedrich,E.L., Heisig,P., Seeber,S., Pommier,Y. and Strumberg,D. (2004) A mutation in Escherichia coli DNA gyrase conferring quinolone resistance results in sensitivity to drugs targeting eukaryotic topoisomerase II. Antimicrob. Agents Chemother., 48, 4495-4504.
-
(2004)
Antimicrob. Agents Chemother.
, vol.48
, pp. 4495-4504
-
-
Gruger, T.1
Nitiss, J.L.2
Maxwell, A.3
Zechiedrich, E.L.4
Heisig, P.5
Seeber, S.6
Pommier, Y.7
Strumberg, D.8
-
43
-
-
11144257689
-
Random mutagenesis of the B′A′ core domain of yeast DNA topoisomerase II and large-scale screens of mutants resistant to the anticancer drug etoposide
-
Jiang,X. (2005) Random mutagenesis of the B′A′ core domain of yeast DNA topoisomerase II and large-scale screens of mutants resistant to the anticancer drug etoposide. Biochem. Biophys. Res. Commun, 327, 597-603.
-
(2005)
Biochem. Biophys. Res. Commun
, vol.327
, pp. 597-603
-
-
Jiang, X.1
-
44
-
-
0141940254
-
Modulation of drug sensitivity in yeast cells by the ATP-binding domain of human DNA topoisomerase IIalpha
-
Vilain,N., Tsai-Pflugfelder,M., Benoit,A., Gasser,S.M. and Leroy,D. (2003) Modulation of drug sensitivity in yeast cells by the ATP-binding domain of human DNA topoisomerase IIalpha. Nucleic Acids Res, 31, 5714-5722.
-
(2003)
Nucleic Acids Res
, vol.31
, pp. 5714-5722
-
-
Vilain, N.1
Tsai-Pflugfelder, M.2
Benoit, A.3
Gasser, S.M.4
Leroy, D.5
-
45
-
-
0141591551
-
Structure of the topoisomerase II ATPase region and its mechanism of inhibition by the chemotherapeutic agent ICRF-187
-
Classen,S., Olland,S. and Berger,J.M. (2003) Structure of the topoisomerase II ATPase region and its mechanism of inhibition by the chemotherapeutic agent ICRF-187. Proc. Natl Acad. Sci. USA, 100, 10629-10634.
-
(2003)
Proc. Natl Acad. Sci. USA
, vol.100
, pp. 10629-10634
-
-
Classen, S.1
Olland, S.2
Berger, J.M.3
-
46
-
-
0029909081
-
The combination of different types of antitumor topoisomerase II inhibitors, ICRF-193 and VP-16, has synergistic and antagonistic effects on cell survival, depending on treatment schedule
-
Ishida,R., Iwai,M., Hara,A. and Andoh,T. (1996) The combination of different types of antitumor topoisomerase II inhibitors, ICRF-193 and VP-16, has synergistic and antagonistic effects on cell survival, depending on treatment schedule. Anticancer Res., 16, 2735-2740.
-
(1996)
Anticancer Res.
, vol.16
, pp. 2735-2740
-
-
Ishida, R.1
Iwai, M.2
Hara, A.3
Andoh, T.4
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