-
1
-
-
0026515757
-
Quinone chemistry and toxicity
-
Monks TJ, Hanzlik RP, Cohen GM, Ross D, Graham DG. Quinone chemistry and toxicity. Toxicol Appl Pharmacol 1992; 112:2-16.
-
(1992)
Toxicol Appl Pharmacol
, vol.112
, pp. 2-16
-
-
Monks, T.J.1
Hanzlik, R.P.2
Cohen, G.M.3
Ross, D.4
Graham, D.G.5
-
2
-
-
0001885549
-
Anthracyclines
-
Chabner BA, Collins JM (editors). Philadelphia, PA: Lippincott
-
Myers CE, Chabner BA. Anthracyclines. In: Chabner BA, Collins JM (editors): Cancer Chemotherapy: Principles and Practice. Philadelphia, PA: Lippincott; 1990, pp. 356-381.
-
(1990)
Cancer Chemotherapy: Principles and Practice
, pp. 356-381
-
-
Myers, C.E.1
Chabner, B.A.2
-
4
-
-
0024316466
-
DNA topoisomerase poisons as antitumor drugs
-
Liu LF. DNA topoisomerase poisons as antitumor drugs. Annu Rev Biochem 1989; 58:351-375.
-
(1989)
Annu Rev Biochem
, vol.58
, pp. 351-375
-
-
Liu, L.F.1
-
5
-
-
0025090826
-
Modulation of doxorubicin-induced chromosomal damage by calmodulin inhibitors and its relationship to cytotoxicity in progressively doxorubicin-resistant tumor cells
-
Ganapathi R, Grabowski D, Hoeltge G, Neelon R. Modulation of doxorubicin-induced chromosomal damage by calmodulin inhibitors and its relationship to cytotoxicity in progressively doxorubicin-resistant tumor cells. Biochem Pharmacol 1990; 40:1657-1662.
-
(1990)
Biochem Pharmacol
, vol.40
, pp. 1657-1662
-
-
Ganapathi, R.1
Grabowski, D.2
Hoeltge, G.3
Neelon, R.4
-
6
-
-
0027278808
-
Apoptosis induced by anthracycline antibiotics in P388 parent and multidrug-resistant cells
-
Ling Y-H, Priebe W, Perez-Soler R. Apoptosis induced by anthracycline antibiotics in P388 parent and multidrug-resistant cells. Cancer Res 1993; 53:1845-1852.
-
(1993)
Cancer Res
, vol.53
, pp. 1845-1852
-
-
Ling, Y.-H.1
Priebe, W.2
Perez-Soler, R.3
-
7
-
-
0030775164
-
Bcl-2 and mdr-1 gene expression during doxorubicin-induced apoptosis in murine leukemic P388 and P388/R84 cells
-
Ramachandran C, You W, Krishan A. Bcl-2 and mdr-1 gene expression during doxorubicin-induced apoptosis in murine leukemic P388 and P388/R84 cells. Anticancer Res 1997; 17:3369-3376.
-
(1997)
Anticancer Res
, vol.17
, pp. 3369-3376
-
-
Ramachandran, C.1
You, W.2
Krishan, A.3
-
8
-
-
0000146455
-
Triptycenes: A novel synthetic class of bifunctional anticancer drugs that inhibit nucleoside transport, induce DNA cleavage and decrease the viability of leukemic cells in the nanomolar range in vitro
-
Perchellet EM, Magill MJ, Huang X, Brantis CE, Hua DH, Perchellet JP. Triptycenes: a novel synthetic class of bifunctional anticancer drugs that inhibit nucleoside transport, induce DNA cleavage and decrease the viability of leukemic cells in the nanomolar range in vitro. Anticancer Drugs 1999; 10:749-766.
-
(1999)
Anticancer Drugs
, vol.10
, pp. 749-766
-
-
Perchellet, E.M.1
Magill, M.J.2
Huang, X.3
Brantis, C.E.4
Hua, D.H.5
Perchellet, J.P.6
-
9
-
-
0036021016
-
Among substituted 9,10-dihydro-9,10-[1,2]benzenoanthracene-4,5,8-tetraones, the lead antitumor triptycene bisquinone TT24 blocks nucleoside transport, induces apoptotic DNA fragmentation and decreases the viability of L1210 leukemic cells in the nanomolar range of daunorubicin in vitro
-
Perchellet EM, Sperfslage BJ, Wang Y, et al. Among substituted 9,10-dihydro-9,10-[1,2]benzenoanthracene-4,5,8-tetraones, the lead antitumor triptycene bisquinone TT24 blocks nucleoside transport, induces apoptotic DNA fragmentation and decreases the viability of L1210 leukemic cells in the nanomolar range of daunorubicin in vitro. Anticancer Drugs 2002; 13:567-582.
-
(2002)
Anticancer Drugs
, vol.13
, pp. 567-582
-
-
Perchellet, E.M.1
Sperfslage, B.J.2
Wang, Y.3
-
10
-
-
0035656150
-
A synthetic triptycene bisquinone, which blocks nucleoside transport and induces DNA fragmentation, retains its cytotoxic efficacy in daunorubiein-resistant HL-60 cell lines
-
Wang B, Wu M, Perchellet EM, et al. A synthetic triptycene bisquinone, which blocks nucleoside transport and induces DNA fragmentation, retains its cytotoxic efficacy in daunorubiein-resistant HL-60 cell lines. Int J Oncol 2001; 19:1169-1178.
-
(2001)
Int J Oncol
, vol.19
, pp. 1169-1178
-
-
Wang, B.1
Wu, M.2
Perchellet, E.M.3
-
11
-
-
0034630317
-
Apoptotic DNA fragmentation
-
Nagata S. Apoptotic DNA fragmentation. Exp Cell Res 2000; 256:12-18.
-
(2000)
Exp Cell Res
, vol.256
, pp. 12-18
-
-
Nagata, S.1
-
12
-
-
0031298259
-
Cleavage of poly(ADP-ribose) polymerase: A sensitive parameter to study cell death
-
Duriez PJ, Shah GM. Cleavage of poly(ADP-ribose) polymerase: a sensitive parameter to study cell death. Biochem Cell Biol 1997; 75:337-349.
-
(1997)
Biochem Cell Biol
, vol.75
, pp. 337-349
-
-
Duriez, P.J.1
Shah, G.M.2
-
13
-
-
0035796025
-
Functions of poly(ADP-ribose) polymerase (PARP) in DNA repair, genomic integrity and cell death
-
Herceg Z, Wang ZQ. Functions of poly(ADP-ribose) polymerase (PARP) in DNA repair, genomic integrity and cell death. Mutat Res 2001; 477:97-110.
-
(2001)
Mutat Res
, vol.477
, pp. 97-110
-
-
Herceg, Z.1
Wang, Z.Q.2
-
14
-
-
0028990125
-
Yama/CPP32 beta, a mammalian homolog of CED-3, is a CrmA-inhibitable protease that cleaves the death substrate poly(ADP-ribose) polymerase
-
Tewari M, Quan LT, O'Rourke K, et al. Yama/CPP32 beta, a mammalian homolog of CED-3, is a CrmA-inhibitable protease that cleaves the death substrate poly(ADP-ribose) polymerase. Cell 1995; 81:801-809.
-
(1995)
Cell
, vol.81
, pp. 801-809
-
-
Tewari, M.1
Quan, L.T.2
O'Rourke, K.3
-
15
-
-
0030187244
-
Proteolytic cleavage during chemotherapy-induced apoptosis
-
Kaufmann SH. Proteolytic cleavage during chemotherapy-induced apoptosis. Mol Med Today 1996; 2:298-303.
-
(1996)
Mol Med Today
, vol.2
, pp. 298-303
-
-
Kaufmann, S.H.1
-
16
-
-
0037114350
-
Induction of poly(ADP-ribose) polymerase-1 cleavage by antitumor triptycene bisquinones in wild-type and daunorubicin-resistant HL-60 cell lines
-
Wang Y, Perchellet EM, Tamura M, Hua DH, Perchellet JP. Induction of poly(ADP-ribose) polymerase-1 cleavage by antitumor triptycene bisquinones in wild-type and daunorubicin-resistant HL-60 cell lines. Cancer Lett 2002; 188:73-83.
-
(2002)
Cancer Lett
, vol.188
, pp. 73-83
-
-
Wang, Y.1
Perchellet, E.M.2
Tamura, M.3
Hua, D.H.4
Perchellet, J.P.5
-
17
-
-
0029144134
-
Topoisomerase poisons: Harnessing the dark side of enzyme mechanism
-
Froelich-Ammon SJ, Osheroff N. Topoisomerase poisons: harnessing the dark side of enzyme mechanism. J Biol Chem 1995; 270:21429-21432.
-
(1995)
J Biol Chem
, vol.270
, pp. 21429-21432
-
-
Froelich-Ammon, S.J.1
Osheroff, N.2
-
19
-
-
0029731177
-
Beyond DNA cross-linking: History and prospect of DNA-targeted cancer treatment. Fifteenth Bruce F. Cain Memorial Award lecture
-
Kohn KW. Beyond DNA cross-linking: history and prospect of DNA-targeted cancer treatment. Fifteenth Bruce F. Cain Memorial Award lecture. Cancer Res 1996; 56:5533-5546.
-
(1996)
Cancer Res
, vol.56
, pp. 5533-5546
-
-
Kohn, K.W.1
-
20
-
-
0026720052
-
The topoisomerase II inhibitor teniposide (VM-26) induces apoptosis in unstimulated mature murine lymphocytes
-
Roy C, Brown DL, Little JE, et al. The topoisomerase II inhibitor teniposide (VM-26) induces apoptosis in unstimulated mature murine lymphocytes. Exp Cell Res 1992; 200:416-424.
-
(1992)
Exp Cell Res
, vol.200
, pp. 416-424
-
-
Roy, C.1
Brown, D.L.2
Little, J.E.3
-
21
-
-
0027498112
-
Topoisomerase inhibitors induce apoptosis in thymocytes
-
Onishi Y, Azuma Y, Sato Y, Mizuno Y, Tadakuma T, Kizaki H. Topoisomerase inhibitors induce apoptosis in thymocytes. Biochim Biophys Acta 1993; 1175:147-154.
-
(1993)
Biochim Biophys Acta
, vol.1175
, pp. 147-154
-
-
Onishi, Y.1
Azuma, Y.2
Sato, Y.3
Mizuno, Y.4
Tadakuma, T.5
Kizaki, H.6
-
22
-
-
0035029153
-
Tumor cell death induced by topoisomerase-targeting drugs
-
Li T-K, Liu LF. Tumor cell death induced by topoisomerase-targeting drugs. Annu Rev Pharmacol Toxicol 2001; 41:53-77.
-
(2001)
Annu Rev Pharmacol Toxicol
, vol.41
, pp. 53-77
-
-
Li, T.-K.1
Liu, L.F.2
-
23
-
-
0024420685
-
Arrest of replication forks by drug-stabilized topoisomerase I-DNA cleavable complexes as a mechanism of cell killing by camptothecin
-
Hsiang Y-H, Lihou MG, Liu LF. Arrest of replication forks by drug-stabilized topoisomerase I-DNA cleavable complexes as a mechanism of cell killing by camptothecin. Cancer Res 1989; 49:5077-5082.
-
(1989)
Cancer Res
, vol.49
, pp. 5077-5082
-
-
Hsiang, Y.-H.1
Lihou, M.G.2
Liu, L.F.3
-
24
-
-
0024388737
-
Differential requirement of DNA replication for the cytotoxicity of DNA topoisomerase I and II inhibitors in Chinese hamster DC3F cells
-
Holm C, Covey JM, Kerrigan D, Pommier Y. Differential requirement of DNA replication for the cytotoxicity of DNA topoisomerase I and II inhibitors in Chinese hamster DC3F cells. Cancer Res 1989; 49:6365-6368.
-
(1989)
Cancer Res
, vol.49
, pp. 6365-6368
-
-
Holm, C.1
Covey, J.M.2
Kerrigan, D.3
Pommier, Y.4
-
25
-
-
0025133118
-
Involvement of nucleic acid synthesis in cell killing mechanisms of topoisomerase poisons
-
D'Arpa P, Beardmore C, Liu LF. Involvement of nucleic acid synthesis in cell killing mechanisms of topoisomerase poisons. Cancer Res 1990; 50:6919-6924.
-
(1990)
Cancer Res
, vol.50
, pp. 6919-6924
-
-
D'Arpa, P.1
Beardmore, C.2
Liu, L.F.3
-
26
-
-
0027137938
-
Intoplicine (RP 60475) and its derivatives, a new class of antitumor agents inhibiting both topoisomerase I and II activities
-
Riou J-F, Fossé P, Nguyen CH, et al. Intoplicine (RP 60475) and its derivatives, a new class of antitumor agents inhibiting both topoisomerase I and II activities. Cancer Res 1993; 63:5987-5993.
-
(1993)
Cancer Res
, vol.63
, pp. 5987-5993
-
-
Riou, J.-F.1
Fossé, P.2
Nguyen, C.H.3
-
27
-
-
0025866667
-
Induction of mammalian DNA topoisomerase I and II-mediated DNA cleavage by saintopin, a new antitumor agent from fungus
-
Yamashita Y, Kawada S, Fujii N, Nakano H. Induction of mammalian DNA topoisomerase I and II-mediated DNA cleavage by saintopin, a new antitumor agent from fungus. Biochemistry 1991; 30:5838-5845.
-
(1991)
Biochemistry
, vol.30
, pp. 5838-5845
-
-
Yamashita, Y.1
Kawada, S.2
Fujii, N.3
Nakano, H.4
-
28
-
-
0025303197
-
Effects of morpholinyl doxorubicins, doxorubicin, and actinomycin D on mammalian DNA topoisomerases I and II
-
Wassermann K, Markovits J, Jaxel C, Capranico G, Kohn KW, Pommier Y. Effects of morpholinyl doxorubicins, doxorubicin, and actinomycin D on mammalian DNA topoisomerases I and II. Mol Pharmacol 1990; 38:38-45.
-
(1990)
Mol Pharmacol
, vol.38
, pp. 38-45
-
-
Wassermann, K.1
Markovits, J.2
Jaxel, C.3
Capranico, G.4
Kohn, K.W.5
Pommier, Y.6
-
29
-
-
0027369170
-
The antileukemic alkaloid fagaronine is an inhibitor of DNA topoisomerases I and II
-
Larsen AK, Grondard L, Couprie J, et al. The antileukemic alkaloid fagaronine is an inhibitor of DNA topoisomerases I and II. Biochem Pharmcol 1993; 46:1403-1412.
-
(1993)
Biochem Pharmcol
, vol.46
, pp. 1403-1412
-
-
Larsen, A.K.1
Grondard, L.2
Couprie, J.3
-
30
-
-
0025719308
-
Inhibition of eukaryotic DNA topoisomerase I and II activities by indoloquinolinedione derivatives
-
Riou JF, Helissey P, Grondard L, Giorgi-Renault S. Inhibition of eukaryotic DNA topoisomerase I and II activities by indoloquinolinedione derivatives. Mol Pharmacol 1991; 40:699-706.
-
(1991)
Mol Pharmacol
, vol.40
, pp. 699-706
-
-
Riou, J.F.1
Helissey, P.2
Grondard, L.3
Giorgi-Renault, S.4
-
31
-
-
0030659850
-
Antitumor activity of a novel quinoline derivative, TAS-103, with inhibitory effects on topoisomerases I and II
-
Utsugi T, Aoyagi K, Asao T, et al. Antitumor activity of a novel quinoline derivative, TAS-103, with inhibitory effects on topoisomerases I and II. Jpn J Cancer Res 1997; 88:992-1002.
-
(1997)
Jpn J Cancer Res
, vol.88
, pp. 992-1002
-
-
Utsugi, T.1
Aoyagi, K.2
Asao, T.3
-
32
-
-
0029893321
-
From amsacrine to DACA (N-[2-(dimethylamino)ethyl]acridine-4-carboxamide): Selectivity for topoisomerases I and II among acridine derivatives
-
Finlay GJ, Riou JF, Baguley BC. From amsacrine to DACA (N-[2-(dimethylamino)ethyl]acridine-4-carboxamide): selectivity for topoisomerases I and II among acridine derivatives. Eur J Cancer 1996; 32A:708-714.
-
(1996)
Eur J Cancer
, vol.32 A
, pp. 708-714
-
-
Finlay, G.J.1
Riou, J.F.2
Baguley, B.C.3
-
33
-
-
0036180994
-
In vitro and in vivo characterization of XR11576, a novel, orally active, dual inhibitor of topoisomerase I and II
-
Mistry P, Stewart AJ, Dangerfield W, et al. In vitro and in vivo characterization of XR11576, a novel, orally active, dual inhibitor of topoisomerase I and II. Anticancer Drugs 2002; 13:15-28.
-
(2002)
Anticancer Drugs
, vol.13
, pp. 15-28
-
-
Mistry, P.1
Stewart, A.J.2
Dangerfield, W.3
-
34
-
-
0033962122
-
F 11782, a novel epipodophylloid non-intercalating dual catalytic inhibitor of topoisomerases I and II with an original mechanism action
-
Perrin D, vanHille B, Barret J-M, et al. F 11782, a novel epipodophylloid non-intercalating dual catalytic inhibitor of topoisomerases I and II with an original mechanism action. Biochem Pharmacol 2000; 59:807-819.
-
(2000)
Biochem Pharmacol
, vol.59
, pp. 807-819
-
-
Perrin, D.1
VanHille, B.2
Barret, J.-M.3
-
35
-
-
0037334275
-
Apoptotic cell death induction by F 11782 a novel dual catalytic inhibitor of topoisomerases I and II
-
Etiévant C, Kruczynski A, Barret J-M, Perrin D, Hill BT. Apoptotic cell death induction by F 11782 a novel dual catalytic inhibitor of topoisomerases I and II. Biochem Pharmacol 2003; 65:755-763.
-
(2003)
Biochem Pharmacol
, vol.65
, pp. 755-763
-
-
Etiévant, C.1
Kruczynski, A.2
Barret, J.-M.3
Perrin, D.4
Hill, B.T.5
-
36
-
-
0036784064
-
Inhibition of DNA topoisomerases II and/or I by pyrazolo[1,5-a]indole derivatives and their growth inhibitory activities
-
Umemura K, Mizushima T, Katayama H, Kiryu Y, Yamori T, Andoh T. Inhibition of DNA topoisomerases II and/or I by pyrazolo[1,5-a]indole derivatives and their growth inhibitory activities. Mol Pharmacol 2002; 62:873-880.
-
(2002)
Mol Pharmacol
, vol.62
, pp. 873-880
-
-
Umemura, K.1
Mizushima, T.2
Katayama, H.3
Kiryu, Y.4
Yamori, T.5
Andoh, T.6
-
37
-
-
0036471448
-
Selective inhibition of the activities of both eukaryotic DNA polymerases and DNA topoisomerases by elenic acid
-
Mizushina Y, Murakami C, Ohta K, et al. Selective inhibition of the activities of both eukaryotic DNA polymerases and DNA topoisomerases by elenic acid. Biochem Pharmacol 2002; 63:399-407.
-
(2002)
Biochem Pharmacol
, vol.63
, pp. 399-407
-
-
Mizushina, Y.1
Murakami, C.2
Ohta, K.3
-
38
-
-
0028948095
-
The dietary anticancer agent ellagic acid is a potent inhibitor of DNA topoisomerases in vitro
-
Constantinou A, Stoner GD, Mehta R, Rao K, Runyan C, Moon R. The dietary anticancer agent ellagic acid is a potent inhibitor of DNA topoisomerases in vitro. Nutr Cancer 1996; 23:121-130.
-
(1996)
Nutr Cancer
, vol.23
, pp. 121-130
-
-
Constantinou, A.1
Stoner, G.D.2
Mehta, R.3
Rao, K.4
Runyan, C.5
Moon, R.6
-
40
-
-
0037012889
-
Syntheses and bioactivities of substituted 9,10-dihydro-9,10-[1,2]benzenoanthracene-1,4,5,8-tetraones. Unusual reactivities with amines
-
Hua DH, Tamura M, Huang X, et al. Syntheses and bioactivities of substituted 9,10-dihydro-9,10-[1,2]benzenoanthracene-1,4,5,8-tetraones. Unusual reactivities with amines. J Org Chem 2002; 67:2907-2912.
-
(2002)
J Org Chem
, vol.67
, pp. 2907-2912
-
-
Hua, D.H.1
Tamura, M.2
Huang, X.3
-
41
-
-
0025899234
-
Use of an aqueous soluble tetrazolium/formazan assay for cell growth assays in culture
-
Cory AH, Owen TC, Barltrop JA, Cory JG. Use of an aqueous soluble tetrazolium/formazan assay for cell growth assays in culture. Cancer Commun 1991; 3:207-212.
-
(1991)
Cancer Commun
, vol.3
, pp. 207-212
-
-
Cory, A.H.1
Owen, T.C.2
Barltrop, J.A.3
Cory, J.G.4
-
42
-
-
0025056628
-
Eukaryotic topoisomerase II preferentially cleaves alternating purine-pyrimidine repeats
-
Spitzner JR, Chung IK, Muller MT. Eukaryotic topoisomerase II preferentially cleaves alternating purine-pyrimidine repeats. Nucleic Acids Res 1990; 18:1-11.
-
(1990)
Nucleic Acids Res
, vol.18
, pp. 1-11
-
-
Spitzner, J.R.1
Chung, I.K.2
Muller, M.T.3
-
43
-
-
0024592332
-
Free radical formation by antitumor quinones
-
Powis G. Free radical formation by antitumor quinones. Free Rad Biol Med 1989; 6:63-101.
-
(1989)
Free Rad Biol Med
, vol.6
, pp. 63-101
-
-
Powis, G.1
-
44
-
-
0032189942
-
Investigating the biological functions of DNA topoisomerases in eukaryotic cells
-
Nitiss JL. Investigating the biological functions of DNA topoisomerases in eukaryotic cells. Biochim Biophys Acta 1998; 1400:63-81.
-
(1998)
Biochim Biophys Acta
, vol.1400
, pp. 63-81
-
-
Nitiss, J.L.1
-
45
-
-
0036085460
-
Cellular roles of DNA topoisomerases: A molecular perspective
-
Wang JC. Cellular roles of DNA topoisomerases: a molecular perspective. Nat Rev Mol Cell Biol 2002; 3:430-440.
-
(2002)
Nat Rev Mol Cell Biol
, vol.3
, pp. 430-440
-
-
Wang, J.C.1
-
46
-
-
0034923502
-
DNA topoisomerases: Structure, function, and mechanism
-
Champoux JJ. DNA topoisomerases: structure, function, and mechanism. Annu Rev Biochem 2001; 70:369-413.
-
(2001)
Annu Rev Biochem
, vol.70
, pp. 369-413
-
-
Champoux, J.J.1
-
47
-
-
0032189683
-
Mechanism of action of eukaryotic DNA topoisomerase I and drugs targeted to the enzyme
-
Pommier Y, Pourquier P, Fan Y, Strumberg D. Mechanism of action of eukaryotic DNA topoisomerase I and drugs targeted to the enzyme. Biochim Biophys Acta 1998; 1400:83-105.
-
(1998)
Biochim Biophys Acta
, vol.1400
, pp. 83-105
-
-
Pommier, Y.1
Pourquier, P.2
Fan, Y.3
Strumberg, D.4
-
48
-
-
0037130269
-
Sequence-specific interactions of drugs interfering with the topoisomerase-DNA cleavage complex
-
Palumbo M, Gatto B, More S, Sissi C, Zagotto G. Sequence-specific interactions of drugs interfering with the topoisomerase-DNA cleavage complex. Biochim Biophys Acta 2002; 1587:145-154.
-
(2002)
Biochim Biophys Acta
, vol.1587
, pp. 145-154
-
-
Palumbo, M.1
Gatto, B.2
More, S.3
Sissi, C.4
Zagotto, G.5
-
50
-
-
0035724690
-
DNA topoisomerases as targets for anticancer drugs
-
Topcu Z. DNA topoisomerases as targets for anticancer drugs. J Clin Pharm Ther 2001; 26:405-416.
-
(2001)
J Clin Pharm Ther
, vol.26
, pp. 405-416
-
-
Topcu, Z.1
-
51
-
-
0036287867
-
DNA topoisomerase II as a target for cancer chemotherapy
-
Walker JV, Nitiss JL. DNA topoisomerase II as a target for cancer chemotherapy. Cancer Invest 2002; 20:570-589.
-
(2002)
Cancer Invest
, vol.20
, pp. 570-589
-
-
Walker, J.V.1
Nitiss, J.L.2
-
52
-
-
0025758625
-
Effects of antineoplastic drugs on the post-strand-passage DNA cleavage/religation equilibrium of topoisomerase II
-
Robinson MJ, Osheroff N. Effects of antineoplastic drugs on the post-strand-passage DNA cleavage/religation equilibrium of topoisomerase II. Biochemistry 1991; 30:1807-1813.
-
(1991)
Biochemistry
, vol.30
, pp. 1807-1813
-
-
Robinson, M.J.1
Osheroff, N.2
-
53
-
-
0030713374
-
Azatoxin is a mechanistic hybrid of the topoisomerase II-targeted anticancer drugs etoposide and ellipticine
-
Cline SD, Macdonald TL, Osheroff N. Azatoxin is a mechanistic hybrid of the topoisomerase II-targeted anticancer drugs etoposide and ellipticine. Biochemistry 1997; 36:13095-13101.
-
(1997)
Biochemistry
, vol.36
, pp. 13095-13101
-
-
Cline, S.D.1
Macdonald, T.L.2
Osheroff, N.3
-
54
-
-
0018639773
-
DNA gyrase: Purification and catalytic properties of a fragment of gyrase B protein
-
Gellert M, Fisher LM, O'Dea MH. DNA gyrase: purification and catalytic properties of a fragment of gyrase B protein. Proc Natl Acad Sci USA 1979; 76:6289-6293.
-
(1979)
Proc Natl Acad Sci USA
, vol.76
, pp. 6289-6293
-
-
Gellert, M.1
Fisher, L.M.2
O'Dea, M.H.3
-
55
-
-
1842319108
-
Energy coupling in DNA gyrase and the mechanism of action of novobiocin
-
Sugino A, Higgins NP, Brown PC, Peebles CL, Cozzarelli NR. Energy coupling in DNA gyrase and the mechanism of action of novobiocin. Proc Natl Acad Sci USA 1978; 75:4838-4842.
-
(1978)
Proc Natl Acad Sci USA
, vol.75
, pp. 4838-4842
-
-
Sugino, A.1
Higgins, N.P.2
Brown, P.C.3
Peebles, C.L.4
Cozzarelli, N.R.5
-
56
-
-
0022400533
-
DNA topoisomerase II is required at the time of mitosis in yeast
-
Holm C, Goto T, Wang JC, Botstein D. DNA topoisomerase II is required at the time of mitosis in yeast. Cell 1985; 41:553-563.
-
(1985)
Cell
, vol.41
, pp. 553-563
-
-
Holm, C.1
Goto, T.2
Wang, J.C.3
Botstein, D.4
-
57
-
-
0024389052
-
A rapid and quantitative microtiter assay for eukaryotic topoisomerase II
-
Muller MT, Helal K, Soisson S, Spitzner JR. A rapid and quantitative microtiter assay for eukaryotic topoisomerase II. Nucleic Acids Res 1989; 17:9499.
-
(1989)
Nucleic Acids Res
, vol.17
, pp. 9499
-
-
Muller, M.T.1
Helal, K.2
Soisson, S.3
Spitzner, J.R.4
-
58
-
-
0021955171
-
Quantitation of eukaryotic topoisomerase I reactivity with DNA. Preferential cleavage of supercoiled DNA
-
Muller MT. Quantitation of eukaryotic topoisomerase I reactivity with DNA. Preferential cleavage of supercoiled DNA. Biochim Biophys Acta 1985; 824:263-267.
-
(1985)
Biochim Biophys Acta
, vol.824
, pp. 263-267
-
-
Muller, M.T.1
-
59
-
-
0028099438
-
Inhibition of topoisomerase I by anthracycline antibiotics: Evidence for general inhibition of topoisomerase I by DNA-binding agents
-
Crow RT, Crothers DM. Inhibition of topoisomerase I by anthracycline antibiotics: evidence for general inhibition of topoisomerase I by DNA-binding agents. J Med Chem 1994; 37:3191-3194.
-
(1994)
J Med Chem
, vol.37
, pp. 3191-3194
-
-
Crow, R.T.1
Crothers, D.M.2
-
60
-
-
0034937266
-
Mitochondria as targets for established and novel anti-cancer agents
-
Grad JM, Cepero E, Boise LH. Mitochondria as targets for established and novel anti-cancer agents. Drug Resistance Updates 2001; 4:85-91.
-
(2001)
Drug Resistance Updates
, vol.4
, pp. 85-91
-
-
Grad, J.M.1
Cepero, E.2
Boise, L.H.3
-
61
-
-
0023971164
-
Stabilization of type I topoisomerase-DNA covalent complexes by actinomycin D
-
Trask DK, Muller MT. Stabilization of type I topoisomerase-DNA covalent complexes by actinomycin D. Proc Natl Acad Sci USA 1988; 85:1417-1421.
-
(1988)
Proc Natl Acad Sci USA
, vol.85
, pp. 1417-1421
-
-
Trask, D.K.1
Muller, M.T.2
-
62
-
-
0030827993
-
Aclacinomycin A stabilizes topoisomerase I covalent complexes
-
Nitiss J L, Pourquier P, Pommier Y. Aclacinomycin A stabilizes topoisomerase I covalent complexes. Cancer Res 1997; 57:4564-4569.
-
(1997)
Cancer Res
, vol.57
, pp. 4564-4569
-
-
Nitiss, J.L.1
Pourquier, P.2
Pommier, Y.3
|