-
1
-
-
0026320118
-
Phase II study of amonafide in advanced breast cancer
-
Scheithauer W, Dittrich C, Kornek G, Haider K, Linkesch W, Gisslinger H, Depisch D. Phase II study of amonafide in advanced breast cancer. Breast Cancer Res Treat 1991; 20:63-7.
-
(1991)
Breast Cancer Res Treat
, vol.20
, pp. 63-67
-
-
Scheithauer, W.1
Dittrich, C.2
Kornek, G.3
Haider, K.4
Linkesch, W.5
Gisslinger, H.6
Depisch, D.7
-
2
-
-
0029041153
-
Amonafide: An active agent in the treatment of previously untreated advanced breast cancer-a cancer and leukemia group B study (CALGB 8642)
-
Costanza ME, Berry D, Henderson IC, Ratain MJ, Wu K, Shapiro C, Duggan D, Kalra J, Berkowitz I, Lyss AP. Amonafide: An active agent in the treatment of previously untreated advanced breast cancer-a cancer and leukemia group B study (CALGB 8642). Clin Cancer Res 1995; 1:699-704.
-
(1995)
Clin Cancer Res
, vol.1
, pp. 699-704
-
-
Costanza, M.E.1
Berry, D.2
Henderson, I.C.3
Ratain, M.J.4
Wu, K.5
Shapiro, C.6
Duggan, D.7
Kalra, J.8
Berkowitz, I.9
Lyss, A.P.10
-
3
-
-
0025947335
-
Paradoxical relationship between acetylator phenotype and amonafide toxicity
-
Ratain MJ, Mick R, Berezin F, Janisch L, Schilsky RL, Williams SF, Smiddy J. Paradoxical relationship between acetylator phenotype and amonafide toxicity. Clin Pharmacol Ther 1991; 50:573-9.
-
(1991)
Clin Pharmacol Ther
, vol.50
, pp. 573-579
-
-
Ratain, M.J.1
Mick, R.2
Berezin, F.3
Janisch, L.4
Schilsky, R.L.5
Williams, S.F.6
Smiddy, J.7
-
4
-
-
0027195119
-
Phase I study of amonafide dosing based on acetylator phenotype
-
Ratain MJ, Mick R, Berezin F, Janisch L, Schilsky RL, Vogelzang NJ, Lane LB. Phase I study of amonafide dosing based on acetylator phenotype. Cancer Res 1993; 53:2304-8.
-
(1993)
Cancer Res
, vol.53
, pp. 2304-2308
-
-
Ratain, M.J.1
Mick, R.2
Berezin, F.3
Janisch, L.4
Schilsky, R.L.5
Vogelzang, N.J.6
Lane, L.B.7
-
5
-
-
33847400139
-
2-M arrest via poisoning topoisomerase II
-
2-M arrest via poisoning topoisomerase II. Molecular cancer therapeutics 2007; 6:484-95.
-
(2007)
Molecular cancer therapeutics
, vol.6
, pp. 484-495
-
-
Zhu, H.1
Huang, M.2
Yang, F.3
Chen, Y.4
Miao, Z.H.5
Qian, X.H.6
Xu, Y.F.7
Qin, Y.X.8
Luo, H.B.9
Shen, X.10
Geng, M.Y.11
Cai, Y.J.12
Ding, J.13
-
6
-
-
0034282984
-
Histological type-selective, tumor-predominant expression of a novel CHK1 isoform and infrequent in vivo somatic CHK2 mutation in small cell lung cancer
-
Haruki N, Saito H, Tatematsu Y, Konishi H, Harano T, Masuda A, Osada H, Fujii Y, Takahashi T. Histological type-selective, tumor-predominant expression of a novel CHK1 isoform and infrequent in vivo somatic CHK2 mutation in small cell lung cancer. Cancer Res 2000; 60:4689-92.
-
(2000)
Cancer Res
, vol.60
, pp. 4689-4692
-
-
Haruki, N.1
Saito, H.2
Tatematsu, Y.3
Konishi, H.4
Harano, T.5
Masuda, A.6
Osada, H.7
Fujii, Y.8
Takahashi, T.9
-
7
-
-
1842691021
-
PI3K/Akt is required for heat shock proteins to protect hypoxia-inducible factor 1alpha from pVHL-independent degradation
-
Zhou J, Schmid T, Frank R, Brune B. PI3K/Akt is required for heat shock proteins to protect hypoxia-inducible factor 1alpha from pVHL-independent degradation. The Journal of biological chemistry 2004; 279:13506-13.
-
(2004)
The Journal of biological chemistry
, vol.279
, pp. 13506-13513
-
-
Zhou, J.1
Schmid, T.2
Frank, R.3
Brune, B.4
-
8
-
-
2942584848
-
Characterization of salvicine-resistant lung adenocarcinoma A549/SAL cell line
-
Miao ZH, Tong LJ, Zhang JS, Han JX, Ding J. Characterization of salvicine-resistant lung adenocarcinoma A549/SAL cell line. Int J Cancer 2004; 110:627-32.
-
(2004)
Int J Cancer
, vol.110
, pp. 627-632
-
-
Miao, Z.H.1
Tong, L.J.2
Zhang, J.S.3
Han, J.X.4
Ding, J.5
-
9
-
-
0035710746
-
Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method
-
Livak KJ, Schmittgen TD. Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method. Methods 2001; 25:402-8.
-
(2001)
Methods
, vol.25
, pp. 402-408
-
-
Livak, K.J.1
Schmittgen, T.D.2
-
10
-
-
24044476837
-
Genotoxic stress targets human Chk1 for degradation by the ubiquitin-proteasome pathway
-
Zhang YW, Otterness DM, Chiang GG, Xie W, Liu YC, Mercurio F, Abraham RT. Genotoxic stress targets human Chk1 for degradation by the ubiquitin-proteasome pathway. Molecular cell 2005; 19:607-18.
-
(2005)
Molecular cell
, vol.19
, pp. 607-618
-
-
Zhang, Y.W.1
Otterness, D.M.2
Chiang, G.G.3
Xie, W.4
Liu, Y.C.5
Mercurio, F.6
Abraham, R.T.7
-
11
-
-
0027980321
-
The ubiquitin-proteasome pathway is required for processing the NFkappaB1 precursor protein and the activation of NFkappaB
-
Palombella VJ, Rando OJ, Goldberg AL, Maniatis T. The ubiquitin-proteasome pathway is required for processing the NFkappaB1 precursor protein and the activation of NFkappaB. Cell 1994; 78:773-85.
-
(1994)
Cell
, vol.78
, pp. 773-785
-
-
Palombella, V.J.1
Rando, O.J.2
Goldberg, A.L.3
Maniatis, T.4
-
12
-
-
0033790297
-
-
Tomoda H, Omura S. Lactacystin, a proteasome inhibitor: discovery and its application in cell biology. Yakugaku Zasshi 2000; 120:935-49.
-
Tomoda H, Omura S. Lactacystin, a proteasome inhibitor: discovery and its application in cell biology. Yakugaku Zasshi 2000; 120:935-49.
-
-
-
-
13
-
-
0026955094
-
Ubiquitin-mediated protein modification and degradation
-
Schwartz AL, Ciechanover A. Ubiquitin-mediated protein modification and degradation. Am J Respir Cell Mol Biol 1992; 7:463-8.
-
(1992)
Am J Respir Cell Mol Biol
, vol.7
, pp. 463-468
-
-
Schwartz, A.L.1
Ciechanover, A.2
-
14
-
-
0347993069
-
Hsp90 inhibition depletes Chk1 and sensitizes tumor cells to replication stress
-
Arlander SJ, Eapen AK, Vroman BT, McDonald RJ, Toft DO, Karnitz LM. Hsp90 inhibition depletes Chk1 and sensitizes tumor cells to replication stress. The Journal of biological chemistry 2003; 278:52572-7.
-
(2003)
The Journal of biological chemistry
, vol.278
, pp. 52572-52577
-
-
Arlander, S.J.1
Eapen, A.K.2
Vroman, B.T.3
McDonald, R.J.4
Toft, D.O.5
Karnitz, L.M.6
-
15
-
-
0030014783
-
DNA topoisomerases
-
Wang JC. DNA topoisomerases. Annu Rev Biochem 1996; 65:635-92.
-
(1996)
Annu Rev Biochem
, vol.65
, pp. 635-692
-
-
Wang, J.C.1
-
16
-
-
0024316466
-
DNA topoisomerase poisons as antitumor drugs
-
Liu LF. DNA topoisomerase poisons as antitumor drugs. Annu Rev Biochem 1989; 58:351-75.
-
(1989)
Annu Rev Biochem
, vol.58
, pp. 351-375
-
-
Liu, L.F.1
-
17
-
-
0035449355
-
Cell cycle checkpoint signaling through the ATM and ATR kinases
-
Abraham RT. Cell cycle checkpoint signaling through the ATM and ATR kinases. Genes & development 2001; 15:2177-96.
-
(2001)
Genes & development
, vol.15
, pp. 2177-2196
-
-
Abraham, R.T.1
-
18
-
-
38949147038
-
2 checkpoint abrogation and checkpoint kinase-1 targeting in the treatment of cancer
-
2 checkpoint abrogation and checkpoint kinase-1 targeting in the treatment of cancer. Br J Cancer 2008; 98:523-8.
-
(2008)
Br J Cancer
, vol.98
, pp. 523-528
-
-
Bucher, N.1
Britten, C.D.2
-
19
-
-
33846636785
-
Chk1 is required for spindle checkpoint function
-
Zachos G, Black EJ, Walker M, Scott MT, Vagnarelli P, Earnshaw WC, Gillespie DA. Chk1 is required for spindle checkpoint function. Developmental cell 2007; 12:247-60.
-
(2007)
Developmental cell
, vol.12
, pp. 247-260
-
-
Zachos, G.1
Black, E.J.2
Walker, M.3
Scott, M.T.4
Vagnarelli, P.5
Earnshaw, W.C.6
Gillespie, D.A.7
-
20
-
-
34247481285
-
Targeting checkpoint kinase 1 in cancer therapeutics
-
Tse AN, Carvajal R, Schwartz GK. Targeting checkpoint kinase 1 in cancer therapeutics. Clin Cancer Res 2007; 13:1955-60.
-
(2007)
Clin Cancer Res
, vol.13
, pp. 1955-1960
-
-
Tse, A.N.1
Carvajal, R.2
Schwartz, G.K.3
|