-
1
-
-
0035237649
-
Chronic myelogenous leukemia
-
Druker B., Sawyers C., Capdeville R., Ford J., Baccarani M., Goldman J. Chronic myelogenous leukemia. Hematology Am Soc Hematol Educ Program 2001, 1:87-112.
-
(2001)
Hematology Am Soc Hematol Educ Program
, vol.1
, pp. 87-112
-
-
Druker, B.1
Sawyers, C.2
Capdeville, R.3
Ford, J.4
Baccarani, M.5
Goldman, J.6
-
2
-
-
0037672877
-
Philadelphia chromosome-positive leukemias: from basic mechanisms to molecular therapeutics
-
Kurzrock R., Kantarjian H., Druker B., Talpaz M. Philadelphia chromosome-positive leukemias: from basic mechanisms to molecular therapeutics. Ann Intern Med 2003, 138:819-830.
-
(2003)
Ann Intern Med
, vol.138
, pp. 819-830
-
-
Kurzrock, R.1
Kantarjian, H.2
Druker, B.3
Talpaz, M.4
-
3
-
-
0034670036
-
The molecular biology of chronic myeloid leukemia
-
Deininger M., Goldman J., Melo J. The molecular biology of chronic myeloid leukemia. Blood 2000, 96:3343-3356.
-
(2000)
Blood
, vol.96
, pp. 3343-3356
-
-
Deininger, M.1
Goldman, J.2
Melo, J.3
-
4
-
-
15944404601
-
The development of imatinib as a therapeutic agent for chronic myeloid leukemia
-
Deininger M., Buchdunger E., Druker B. The development of imatinib as a therapeutic agent for chronic myeloid leukemia. Blood 2005, 105:2640-2653.
-
(2005)
Blood
, vol.105
, pp. 2640-2653
-
-
Deininger, M.1
Buchdunger, E.2
Druker, B.3
-
5
-
-
0041466445
-
Specific targeted therapy of chronic myelogenous leukemia with imatinib
-
Deininger M., Druker B. Specific targeted therapy of chronic myelogenous leukemia with imatinib. Pharmacol Rev 2003, 55:401-423.
-
(2003)
Pharmacol Rev
, vol.55
, pp. 401-423
-
-
Deininger, M.1
Druker, B.2
-
6
-
-
34548825795
-
Bcr-Abl kinase domain mutations, drug resistance, and the road to a cure for chronic myeloid leukemia
-
O'Hare T., Eide C.A., Deininger M.W. Bcr-Abl kinase domain mutations, drug resistance, and the road to a cure for chronic myeloid leukemia. Blood 2007, 110:2242-2249.
-
(2007)
Blood
, vol.110
, pp. 2242-2249
-
-
O'Hare, T.1
Eide, C.A.2
Deininger, M.W.3
-
7
-
-
0001686739
-
Multiple BCR-ABL kinase domain mutations confer polyclonal resistance to the tyrosine kinase inhibitor imatinib (STI571) in chronic phase and blast crisis chronic myeloid leukemia
-
Shah N.P., Nicoll J.M., Nagar B., Gorre M.E., Paquette R.L., Kuriyan J., et al. Multiple BCR-ABL kinase domain mutations confer polyclonal resistance to the tyrosine kinase inhibitor imatinib (STI571) in chronic phase and blast crisis chronic myeloid leukemia. Cancer Cell 2002, 2:99-102.
-
(2002)
Cancer Cell
, vol.2
, pp. 99-102
-
-
Shah, N.P.1
Nicoll, J.M.2
Nagar, B.3
Gorre, M.E.4
Paquette, R.L.5
Kuriyan, J.6
-
8
-
-
44649155314
-
New combination therapies with cell-cycle agents
-
Deep G., Agarwal R. New combination therapies with cell-cycle agents. Curr Opin Investig Drugs 2008, 9:591-604.
-
(2008)
Curr Opin Investig Drugs
, vol.9
, pp. 591-604
-
-
Deep, G.1
Agarwal, R.2
-
9
-
-
0034033865
-
Pyrrolo-1,5-benzoxazepines induce apoptosis in HL-60, Jurkat, and Hut-78 cells: a new class of apoptotic agents
-
Zisterer D.M., Campiani G., Nacci V., Williams D.C. Pyrrolo-1,5-benzoxazepines induce apoptosis in HL-60, Jurkat, and Hut-78 cells: a new class of apoptotic agents. J Pharmacol Exp Ther 2000, 293:48-59.
-
(2000)
J Pharmacol Exp Ther
, vol.293
, pp. 48-59
-
-
Zisterer, D.M.1
Campiani, G.2
Nacci, V.3
Williams, D.C.4
-
10
-
-
0035197959
-
Pyrrolo-1,5-benzoxazepines induce apoptosis in chronic myelogenous leukemia (CML) cells by bypassing the apoptotic suppressor bcr-abl
-
Mc Gee M.M., Campiani G., Ramunno A., Fattorusso C., Nacci V., Lawler M., et al. Pyrrolo-1,5-benzoxazepines induce apoptosis in chronic myelogenous leukemia (CML) cells by bypassing the apoptotic suppressor bcr-abl. J Pharmacol Exp Ther 2001, 296:31-40.
-
(2001)
J Pharmacol Exp Ther
, vol.296
, pp. 31-40
-
-
Mc Gee, M.M.1
Campiani, G.2
Ramunno, A.3
Fattorusso, C.4
Nacci, V.5
Lawler, M.6
-
11
-
-
33745231363
-
Identification of tubulin as the molecular target of proapoptotic pyrrolo-1,5-benzoxazepines
-
Mulligan J.M., Greene L.M., Cloonan S., Mc Gee M.M., Onnis V., Campiani G., et al. Identification of tubulin as the molecular target of proapoptotic pyrrolo-1,5-benzoxazepines. Mol Pharmacol 2006, 70:60-70.
-
(2006)
Mol Pharmacol
, vol.70
, pp. 60-70
-
-
Mulligan, J.M.1
Greene, L.M.2
Cloonan, S.3
Mc Gee, M.M.4
Onnis, V.5
Campiani, G.6
-
12
-
-
0037166238
-
Activation of the c-Jun N-terminal kinase (JNK) signaling pathway is essential during PBOX-6-induced apoptosis in chronic myelogenous leukemia (CML) cells
-
Mc Gee M.M., Campiani G., Ramunno A., Nacci V., Lawler M., Williams D.C., et al. Activation of the c-Jun N-terminal kinase (JNK) signaling pathway is essential during PBOX-6-induced apoptosis in chronic myelogenous leukemia (CML) cells. J Biol Chem 2002, 277:18383-18389.
-
(2002)
J Biol Chem
, vol.277
, pp. 18383-18389
-
-
Mc Gee, M.M.1
Campiani, G.2
Ramunno, A.3
Nacci, V.4
Lawler, M.5
Williams, D.C.6
-
13
-
-
4243195883
-
Selective induction of apoptosis by the pyrrolo-1,5-benzoxazepine 7-[[dimethylcarbamoyl]oxy]-6-(2-naphthyl)pyrrolo-[2,1-d] (1,5)-benzoxazepine (PBOX-6) in leukemia cells occurs via the c-Jun NH2-terminal kinase-dependent phosphorylation and inactivation of Bcl-2 and Bcl-XL
-
Mc Gee M.M., Greene L.M., Ledwidge S., Campiani G., Nacci V., Lawler M., et al. Selective induction of apoptosis by the pyrrolo-1,5-benzoxazepine 7-[[dimethylcarbamoyl]oxy]-6-(2-naphthyl)pyrrolo-[2,1-d] (1,5)-benzoxazepine (PBOX-6) in leukemia cells occurs via the c-Jun NH2-terminal kinase-dependent phosphorylation and inactivation of Bcl-2 and Bcl-XL. J Pharmacol Exp Ther 2004, 310:1084-1095.
-
(2004)
J Pharmacol Exp Ther
, vol.310
, pp. 1084-1095
-
-
Mc Gee, M.M.1
Greene, L.M.2
Ledwidge, S.3
Campiani, G.4
Nacci, V.5
Lawler, M.6
-
14
-
-
70350528658
-
The novel tubulin-targeting agent pyrrolo-1,5-benzoxazepine-15 induces apoptosis in poor prognostic subgroups of chronic lymphocytic leukemia
-
McElligott A.M., Maginn E.N., Greene L.M., McGuckin S., Hayat A., Browne P.V., et al. The novel tubulin-targeting agent pyrrolo-1,5-benzoxazepine-15 induces apoptosis in poor prognostic subgroups of chronic lymphocytic leukemia. Cancer Res 2009, 69:8366-8375.
-
(2009)
Cancer Res
, vol.69
, pp. 8366-8375
-
-
McElligott, A.M.1
Maginn, E.N.2
Greene, L.M.3
McGuckin, S.4
Hayat, A.5
Browne, P.V.6
-
15
-
-
77952287929
-
-
Novel pyrrolo-1,5-benzoxazepine compounds display significant activity against resistant chronic myeloid leukaemia cells in vitro, in ex vivo patient samples and in vivo; 2010 (unpublished results)
-
Bright SA, McElligott AM, O'Connell JW, O'Connor L, Carroll P, Campiani G, et al. Novel pyrrolo-1,5-benzoxazepine compounds display significant activity against resistant chronic myeloid leukaemia cells in vitro, in ex vivo patient samples and in vivo; 2010 (unpublished results).
-
-
-
Bright, S.A.1
McElligott, A.M.2
O'Connell, J.W.3
O'Connor, L.4
Carroll, P.5
Campiani, G.6
-
16
-
-
27744573115
-
The pyrrolo-1,5-benzoxazepine, PBOX-6, inhibits the growth of breast cancer cells in vitro independent of estrogen receptor status and inhibits breast tumour growth in vivo
-
Greene L.M., Fleeton M., Mulligan J., Gowda C., Sheahan B.J., Atkins G.J., et al. The pyrrolo-1,5-benzoxazepine, PBOX-6, inhibits the growth of breast cancer cells in vitro independent of estrogen receptor status and inhibits breast tumour growth in vivo. Oncol Rep 2005, 14:1357-1363.
-
(2005)
Oncol Rep
, vol.14
, pp. 1357-1363
-
-
Greene, L.M.1
Fleeton, M.2
Mulligan, J.3
Gowda, C.4
Sheahan, B.J.5
Atkins, G.J.6
-
17
-
-
33947409844
-
STI-571 enhances the apoptotic efficacy of PBOX-6, a novel microtubule targeting agent, in both STI-571-sensitive and -resistant Bcr-Abl-positive human chronic myeloid leukemia cells
-
Greene L.M., Kelly L., Onnis V., Campiani G., Lawler M., Williams D.C., et al. STI-571 enhances the apoptotic efficacy of PBOX-6, a novel microtubule targeting agent, in both STI-571-sensitive and -resistant Bcr-Abl-positive human chronic myeloid leukemia cells. J Pharmacol Exp Ther 2007, 321:288-297.
-
(2007)
J Pharmacol Exp Ther
, vol.321
, pp. 288-297
-
-
Greene, L.M.1
Kelly, L.2
Onnis, V.3
Campiani, G.4
Lawler, M.5
Williams, D.C.6
-
18
-
-
0033375469
-
Flavopiridol: the first cyclin-dependent kinase inhibitor in human clinical trials
-
Senderowicz A.M. Flavopiridol: the first cyclin-dependent kinase inhibitor in human clinical trials. Invest New Drugs 1999, 17:313-320.
-
(1999)
Invest New Drugs
, vol.17
, pp. 313-320
-
-
Senderowicz, A.M.1
-
19
-
-
3042536038
-
Preclinical and clinical development of the cyclin-dependent kinase inhibitor flavopiridol
-
Shapiro G.I. Preclinical and clinical development of the cyclin-dependent kinase inhibitor flavopiridol. Clin Cancer Res 2004, 10:4270-4275.
-
(2004)
Clin Cancer Res
, vol.10
, pp. 4270-4275
-
-
Shapiro, G.I.1
-
20
-
-
33644830944
-
Targeting the cell cycle: a new approach to cancer therapy
-
Schwartz G.K., Shah M.A. Targeting the cell cycle: a new approach to cancer therapy. J Clin Oncol 2005, 23:9408-9421.
-
(2005)
J Clin Oncol
, vol.23
, pp. 9408-9421
-
-
Schwartz, G.K.1
Shah, M.A.2
-
21
-
-
0043011497
-
Phase II study of flavopiridol in patients with advanced colorectal cancer
-
Aklilu M., Kindler H.L., Donehower R.C., Mani S., Vokes E.E. Phase II study of flavopiridol in patients with advanced colorectal cancer. Ann Oncol 2003, 14:1270-1273.
-
(2003)
Ann Oncol
, vol.14
, pp. 1270-1273
-
-
Aklilu, M.1
Kindler, H.L.2
Donehower, R.C.3
Mani, S.4
Vokes, E.E.5
-
22
-
-
0033955395
-
Flavopiridol, a novel cyclin-dependent kinase inhibitor, in metastatic renal cancer: a University of Chicago Phase II Consortium study
-
Stadler W.M., Vogelzang N.J., Amato R., Sosman J., Taber D., Liebowitz D., et al. Flavopiridol, a novel cyclin-dependent kinase inhibitor, in metastatic renal cancer: a University of Chicago Phase II Consortium study. J Clin Oncol 2000, 18:371-375.
-
(2000)
J Clin Oncol
, vol.18
, pp. 371-375
-
-
Stadler, W.M.1
Vogelzang, N.J.2
Amato, R.3
Sosman, J.4
Taber, D.5
Liebowitz, D.6
-
23
-
-
10744230675
-
A Phase II trial of flavopiridol (NSC #649890) in patients with previously untreated metastatic androgen-independent prostate cancer
-
Liu G., Gandara D.R., Lara P.N.J., Raghavan D., Doroshow J.H., Twardowski P., et al. A Phase II trial of flavopiridol (NSC #649890) in patients with previously untreated metastatic androgen-independent prostate cancer. Clin Cancer Res 2004, 10:924-928.
-
(2004)
Clin Cancer Res
, vol.10
, pp. 924-928
-
-
Liu, G.1
Gandara, D.R.2
Lara, P.N.J.3
Raghavan, D.4
Doroshow, J.H.5
Twardowski, P.6
-
24
-
-
0035300684
-
Phase II study of the cyclin-dependent kinase inhibitor flavopiridol administered to patients with advanced gastric carcinoma
-
Schwartz G.K., Ilson D., Saltz L., O'Reilly E., Tong W., Maslak P., et al. Phase II study of the cyclin-dependent kinase inhibitor flavopiridol administered to patients with advanced gastric carcinoma. J Clin Oncol 2001, 19:1985-1992.
-
(2001)
J Clin Oncol
, vol.19
, pp. 1985-1992
-
-
Schwartz, G.K.1
Ilson, D.2
Saltz, L.3
O'Reilly, E.4
Tong, W.5
Maslak, P.6
-
25
-
-
34848818485
-
Flavopiridol in the treatment of chronic lymphocytic leukemia
-
Christian B.A., Grever M.R., Byrd J.C., Lin T.S. Flavopiridol in the treatment of chronic lymphocytic leukemia. Curr Opin Oncol 2007, 19:573-578.
-
(2007)
Curr Opin Oncol
, vol.19
, pp. 573-578
-
-
Christian, B.A.1
Grever, M.R.2
Byrd, J.C.3
Lin, T.S.4
-
26
-
-
63849246351
-
Clinical response and pharmacokinetics from a phase 1 study of an active dosing schedule of flavopiridol in relapsed chronic lymphocytic leukemia
-
Phelps M.A., Lin T.S., Johnson A.J., Hurh E., Rozewski D.M., Farley K.L., et al. Clinical response and pharmacokinetics from a phase 1 study of an active dosing schedule of flavopiridol in relapsed chronic lymphocytic leukemia. Blood 2009, 113:2637-2645.
-
(2009)
Blood
, vol.113
, pp. 2637-2645
-
-
Phelps, M.A.1
Lin, T.S.2
Johnson, A.J.3
Hurh, E.4
Rozewski, D.M.5
Farley, K.L.6
-
27
-
-
34547650860
-
Sequential flavopiridol, cytosine arabinoside, and mitoxantrone: a phase II trial in adults with poor-risk acute myelogenous leukemia
-
Karp J.E., Smith B.D., Levis M.J., Gore S.D., Greer J., Hattenburg C., et al. Sequential flavopiridol, cytosine arabinoside, and mitoxantrone: a phase II trial in adults with poor-risk acute myelogenous leukemia. Clin Cancer Res 2007, 13:4467-4473.
-
(2007)
Clin Cancer Res
, vol.13
, pp. 4467-4473
-
-
Karp, J.E.1
Smith, B.D.2
Levis, M.J.3
Gore, S.D.4
Greer, J.5
Hattenburg, C.6
-
28
-
-
35348859609
-
Phase I dose-finding study of weekly docetaxel followed by flavopiridol for patients with advanced solid tumors
-
Fornier M.N., Rathkopf D., Shah M., Patil S., O'Reilly E., Tse A.N., et al. Phase I dose-finding study of weekly docetaxel followed by flavopiridol for patients with advanced solid tumors. Clin Cancer Res 2007, 13:5841-5846.
-
(2007)
Clin Cancer Res
, vol.13
, pp. 5841-5846
-
-
Fornier, M.N.1
Rathkopf, D.2
Shah, M.3
Patil, S.4
O'Reilly, E.5
Tse, A.N.6
-
29
-
-
4143122204
-
Phase I trial of the cyclin-dependent kinase inhibitor flavopiridol in combination with docetaxel in patients with metastatic breast cancer
-
Tan A.R., Yang X., Berman A., Zhai S., Sparreboom A., Parr A.L., et al. Phase I trial of the cyclin-dependent kinase inhibitor flavopiridol in combination with docetaxel in patients with metastatic breast cancer. Clin Cancer Res 2004, 10:5038-5047.
-
(2004)
Clin Cancer Res
, vol.10
, pp. 5038-5047
-
-
Tan, A.R.1
Yang, X.2
Berman, A.3
Zhai, S.4
Sparreboom, A.5
Parr, A.L.6
-
30
-
-
45849087334
-
Phase I study of flavopiridol in combination with paclitaxel and carboplatin in patients with non-small-cell lung cancer
-
George S., Kasimis B.S., Cogswell J., Schwarzenberger P., Shapiro G.I., Fidias P., et al. Phase I study of flavopiridol in combination with paclitaxel and carboplatin in patients with non-small-cell lung cancer. Clin Lung Cancer 2008, 9:160-165.
-
(2008)
Clin Lung Cancer
, vol.9
, pp. 160-165
-
-
George, S.1
Kasimis, B.S.2
Cogswell, J.3
Schwarzenberger, P.4
Shapiro, G.I.5
Fidias, P.6
-
31
-
-
0034700154
-
Regulation of apoptosis at cell division by p34cdc2 phosphorylation of survivin
-
O'Connor D.S., Grossman D., Plescia J., Li F., Zhang H., Villa A., et al. Regulation of apoptosis at cell division by p34cdc2 phosphorylation of survivin. Proc Natl Acad Sci USA 2000, 97:13103-13107.
-
(2000)
Proc Natl Acad Sci USA
, vol.97
, pp. 13103-13107
-
-
O'Connor, D.S.1
Grossman, D.2
Plescia, J.3
Li, F.4
Zhang, H.5
Villa, A.6
-
32
-
-
33645463461
-
Targeted therapy by disabling crossroad signaling networks: the survivin paradigm
-
Altieri D.C. Targeted therapy by disabling crossroad signaling networks: the survivin paradigm. Mol Cancer Ther 2006, 5:478-482.
-
(2006)
Mol Cancer Ther
, vol.5
, pp. 478-482
-
-
Altieri, D.C.1
-
33
-
-
0030812207
-
Cytotoxic synergy between flavopiridol (NSC 649890, L86-8275) and various antineoplastic agents: the importance of sequence of administration
-
Bible K.C., Kaufmannm S.H. Cytotoxic synergy between flavopiridol (NSC 649890, L86-8275) and various antineoplastic agents: the importance of sequence of administration. Cancer Res 1997, 57:3375-3380.
-
(1997)
Cancer Res
, vol.57
, pp. 3375-3380
-
-
Bible, K.C.1
Kaufmannm, S.H.2
-
34
-
-
0032804733
-
Sequential dependent enhancement of caspase activation and apoptosis by flavopiridol on paclitaxel-treated human gastric and breast cancer cells
-
Motwani M., Delohery T.M., Schwartz G.K. Sequential dependent enhancement of caspase activation and apoptosis by flavopiridol on paclitaxel-treated human gastric and breast cancer cells. Clin Cancer Res 1999, 7:1876-1883.
-
(1999)
Clin Cancer Res
, vol.7
, pp. 1876-1883
-
-
Motwani, M.1
Delohery, T.M.2
Schwartz, G.K.3
-
35
-
-
0034019911
-
Flavopiridol, a cyclin-dependent kinase inhibitor, prevents spindle inhibitor-induced endoreduplication in human cancer cells
-
Motwani M., Li X., Schwartz G.K. Flavopiridol, a cyclin-dependent kinase inhibitor, prevents spindle inhibitor-induced endoreduplication in human cancer cells. Clin Cancer Res 2000, 6:924-932.
-
(2000)
Clin Cancer Res
, vol.6
, pp. 924-932
-
-
Motwani, M.1
Li, X.2
Schwartz, G.K.3
-
36
-
-
0037228959
-
Suppression of survivin phosphorylation on Thr34 by flavopiridol enhances tumor cell apoptosis
-
Wall N.R., O'Connor D.S., Plescia J., Pommier Y., Altieri D.C. Suppression of survivin phosphorylation on Thr34 by flavopiridol enhances tumor cell apoptosis. Cancer Res 2003, 63:230-235.
-
(2003)
Cancer Res
, vol.63
, pp. 230-235
-
-
Wall, N.R.1
O'Connor, D.S.2
Plescia, J.3
Pommier, Y.4
Altieri, D.C.5
-
37
-
-
43749086323
-
SGX393 inhibits the CML mutant Bcr-AblT315I and preempts in vitro resistance when combined with nilotinib or dasatinib
-
O'Hare T., Eide C.A., Tyner J.W., Corbin A.S., Wong M.J., Buchanan S., et al. SGX393 inhibits the CML mutant Bcr-AblT315I and preempts in vitro resistance when combined with nilotinib or dasatinib. Proc Natl Acad Sci USA 2008, 105:5507-5512.
-
(2008)
Proc Natl Acad Sci USA
, vol.105
, pp. 5507-5512
-
-
O'Hare, T.1
Eide, C.A.2
Tyner, J.W.3
Corbin, A.S.4
Wong, M.J.5
Buchanan, S.6
-
38
-
-
0021118703
-
Quantitative analysis of dose-effect relationships: the combined effects of multiple drugs or enzyme inhibitors
-
Chou T.C., Talalay P. Quantitative analysis of dose-effect relationships: the combined effects of multiple drugs or enzyme inhibitors. Adv Enzyme Regul 1984, 22:27-55.
-
(1984)
Adv Enzyme Regul
, vol.22
, pp. 27-55
-
-
Chou, T.C.1
Talalay, P.2
-
39
-
-
58649117744
-
The novel pyrrolo-1,5-benzoxazepine, PBOX-21, potentiates the apoptotic efficacy of STI571 (imatinib mesylate) in human chronic myeloid leukaemia cells
-
Bright S.A., Greene L.M., Greene T.F., Campiani G., Butini S., Brindisi M., et al. The novel pyrrolo-1,5-benzoxazepine, PBOX-21, potentiates the apoptotic efficacy of STI571 (imatinib mesylate) in human chronic myeloid leukaemia cells. Biochem Pharmacol 2009, 77:310-321.
-
(2009)
Biochem Pharmacol
, vol.77
, pp. 310-321
-
-
Bright, S.A.1
Greene, L.M.2
Greene, T.F.3
Campiani, G.4
Butini, S.5
Brindisi, M.6
-
40
-
-
0035210294
-
Pyrrolo-1,5-benzoxazepines: a new class of apoptotic agents
-
Zisterer D.M., McGee M.M., Campiani G., Ramunno A., Fattorusso C., Nacci V., et al. Pyrrolo-1,5-benzoxazepines: a new class of apoptotic agents. Biochem Soc Trans 2001, 29:704-706.
-
(2001)
Biochem Soc Trans
, vol.29
, pp. 704-706
-
-
Zisterer, D.M.1
McGee, M.M.2
Campiani, G.3
Ramunno, A.4
Fattorusso, C.5
Nacci, V.6
-
41
-
-
38549128934
-
BubR1 is required for a sustained mitotic spindle checkpoint arrest in human cancer cells treated with tubulin-targeting pyrrolo-1,5-benzoxazepines
-
Greene L.M., Campiani G., Lawler M., Williams D.C., Zisterer D.M. BubR1 is required for a sustained mitotic spindle checkpoint arrest in human cancer cells treated with tubulin-targeting pyrrolo-1,5-benzoxazepines. Mol Pharmacol 2008, 73:419-430.
-
(2008)
Mol Pharmacol
, vol.73
, pp. 419-430
-
-
Greene, L.M.1
Campiani, G.2
Lawler, M.3
Williams, D.C.4
Zisterer, D.M.5
-
42
-
-
2442534189
-
Induction of survivin expression by taxol (paclitaxel) is an early event, which is independent of taxol-mediated G2/M arrest
-
Ling X., Bernacki R.J., Brattain M.G., Li F. Induction of survivin expression by taxol (paclitaxel) is an early event, which is independent of taxol-mediated G2/M arrest. J Biol Chem 2004, 279:15196-15203.
-
(2004)
J Biol Chem
, vol.279
, pp. 15196-15203
-
-
Ling, X.1
Bernacki, R.J.2
Brattain, M.G.3
Li, F.4
-
43
-
-
76749118103
-
Multicenter phase II trial of YM155, a small-molecule suppressor of survivin, in patients with advanced, refractory, non-small-cell lung cancer
-
Giaccone G., Zatloukal P., Roubec J., Floor K., Musil J., Kuta M., et al. Multicenter phase II trial of YM155, a small-molecule suppressor of survivin, in patients with advanced, refractory, non-small-cell lung cancer. J Clin Oncol 2009, 27:4481-4486.
-
(2009)
J Clin Oncol
, vol.27
, pp. 4481-4486
-
-
Giaccone, G.1
Zatloukal, P.2
Roubec, J.3
Floor, K.4
Musil, J.5
Kuta, M.6
-
44
-
-
66649126940
-
Phase I study of YM155, a novel survivin suppressant, in patients with advanced solid tumors
-
Satoh T., Okamoto I., Miyazaki M., Morinaga R., Tsuya A., Hasegawa Y., et al. Phase I study of YM155, a novel survivin suppressant, in patients with advanced solid tumors. Clin Cancer Res 2009, 15:3872-3880.
-
(2009)
Clin Cancer Res
, vol.15
, pp. 3872-3880
-
-
Satoh, T.1
Okamoto, I.2
Miyazaki, M.3
Morinaga, R.4
Tsuya, A.5
Hasegawa, Y.6
-
45
-
-
36348998080
-
Phase I/II clinical safety studies of terameprocol vaginal ointment
-
Khanna N., Dalby R., Tan M., Arnold S., Stern J., Frazer N. Phase I/II clinical safety studies of terameprocol vaginal ointment. Gynecol Oncol 2007, 107:554-562.
-
(2007)
Gynecol Oncol
, vol.107
, pp. 554-562
-
-
Khanna, N.1
Dalby, R.2
Tan, M.3
Arnold, S.4
Stern, J.5
Frazer, N.6
-
46
-
-
0036220822
-
Complexities in the development of cyclin-dependent kinase inhibitor drugs
-
Sausville E.A. Complexities in the development of cyclin-dependent kinase inhibitor drugs. Trends Mol Med 2002, 4:S32-S37.
-
(2002)
Trends Mol Med
, vol.4
-
-
Sausville, E.A.1
-
47
-
-
0034661538
-
Protein kinase inhibitors flavopiridol and 7-hydroxy-staurosporine down-regulate antiapoptosis proteins in B-cell chronic lymphocytic leukemia
-
Kitada S., Zapata J.M., Andreeff M., Reed J.C. Protein kinase inhibitors flavopiridol and 7-hydroxy-staurosporine down-regulate antiapoptosis proteins in B-cell chronic lymphocytic leukemia. Blood 2000, 96:393-397.
-
(2000)
Blood
, vol.96
, pp. 393-397
-
-
Kitada, S.1
Zapata, J.M.2
Andreeff, M.3
Reed, J.C.4
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