-
1
-
-
0038100233
-
Molecular mechanisms of transformation by the BCR-ABLoncogene. Se-min
-
Sattler M, Griffin JD. Molecular mechanisms of transformation by the BCR-ABLoncogene. Se-min Hematol. 2003;40:4-10.
-
(2003)
Hematol
, vol.40
, pp. 4-10
-
-
Sattler, M.1
Griffin, J.D.2
-
2
-
-
15944404601
-
The development of imatinib as a therapeutic agent for chronic myeloid leukemia
-
Deininger M, Buchdunger E, Druker BJ. 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.J.3
-
3
-
-
10744233716
-
Imatinib compared with Interferon and low-dose cytara-bine for newly diagnosed chronic-phase chronic myeloid leukemia
-
O'Brien SG, Guilhot F. Larson RA, et al. Imatinib compared with Interferon and low-dose cytara-bine for newly diagnosed chronic-phase chronic myeloid leukemia. N Engl J Med. 2003;348:994-1004.
-
(2003)
N Engl J Med
, vol.348
, pp. 994-1004
-
-
O'Brien, S.G.1
Guilhot, F.2
Larson, R.A.3
-
4
-
-
33745085275
-
OCT-1-mediated influx is a key determinant of the intracellular uptake of imatinib but not nilotinib (AMN107): Reduced OCT-1 activity is the cause of low in vitro sensitivity to imatinib
-
White DL. Saunders VA, Dang P, et al. OCT-1-mediated influx is a key determinant of the intracellular uptake of imatinib but not nilotinib (AMN107): reduced OCT-1 activity is the cause of low in vitro sensitivity to imatinib. Blood. 2006; 108:697-704.
-
(2006)
Blood
, vol.108
, pp. 697-704
-
-
White, D.L.1
Saunders, V.A.2
Dang, P.3
-
5
-
-
0037085785
-
Imatinib induces durable hematologic and cytogenetic responses in patients with accelerated phase chronic myeloid leukemia: Results of a phase 2 study
-
Talpaz M, Silver RT, Druker BJ, et al. Imatinib induces durable hematologic and cytogenetic responses in patients with accelerated phase chronic myeloid leukemia: results of a phase 2 study. Blood. 2002;99:1928-1937.
-
(2002)
Blood
, vol.99
, pp. 1928-1937
-
-
Talpaz, M.1
Silver, R.T.2
Druker, B.J.3
-
6
-
-
0037093092
-
Imatinib induces hematologic and cytogenetic responses in patients with chronic myelogenous leukemia in myeloid blast crisis: Results of a phase II study
-
Sawyers CL; Hochhaus A, Feldman E, et al. Imatinib induces hematologic and cytogenetic responses in patients with chronic myelogenous leukemia in myeloid blast crisis: results of a phase II study. Blood. 2002;99:3530-3539.
-
(2002)
Blood
, vol.99
, pp. 3530-3539
-
-
Sawyers, C.L.1
Hochhaus, A.2
Feldman, E.3
-
7
-
-
0038375012
-
Several Bcr-Abl kinase domain mutants associated with imatinib mesylate resistance remain sensitive to imatinib
-
Corbin AS, La Rosee P, Stoffregen EP, Druker BJ, Deininger MW. Several Bcr-Abl kinase domain mutants associated with imatinib mesylate resistance remain sensitive to imatinib. Blood. 2003; 101:4611-4614.
-
(2003)
Blood
, vol.101
, pp. 4611-4614
-
-
Corbin, A.S.1
La Rosee, P.2
Stoffregen, E.P.3
Druker, B.J.4
Deininger, M.W.5
-
8
-
-
21144451094
-
In vitro activity of Bcr-Abl inhibitors AMN 107 and BMS-354825 against clinically relevant imatinib-resistant Abl kinase domain mutants
-
O'Hare T, Walters DK, Stoffregen EP, et al. In vitro activity of Bcr-Abl inhibitors AMN 107 and BMS-354825 against clinically relevant imatinib-resistant Abl kinase domain mutants. Cancer Res. 2005;65:4500-4505.
-
(2005)
Cancer Res
, vol.65
, pp. 4500-4505
-
-
O'Hare, T.1
Walters, D.K.2
Stoffregen, E.P.3
-
9
-
-
3142676436
-
Overriding imatinib resistance with a novel ABL kinase inhibitor
-
Shah NP, Tran C, Lee FY, Chen P, Norris D, Sawyers CL. Overriding imatinib resistance with a novel ABL kinase inhibitor. Science. 2004;305: 399-401.
-
(2004)
Science
, vol.305
, pp. 399-401
-
-
Shah, N.P.1
Tran, C.2
Lee, F.Y.3
Chen, P.4
Norris, D.5
Sawyers, C.L.6
-
10
-
-
13844251975
-
Characterization of AMN107, a selective inhibitor of native and mutant Bcr-Abl
-
Weisberg E, Manley PW, Breitenstein W, et al. Characterization of AMN107, a selective inhibitor of native and mutant Bcr-Abl. Cancer Cell. 2005; 7:129-141.
-
(2005)
Cancer Cell
, vol.7
, pp. 129-141
-
-
Weisberg, E.1
Manley, P.W.2
Breitenstein, W.3
-
11
-
-
33845806858
-
In vitro and in vivo activity of SKI-606, a novel Src-Abl inhibitor, against imatinib-resistant Bcr-Abl+ neoplastic cells
-
Puttini M, Coluccia AM, Boschelli F, et al. In vitro and in vivo activity of SKI-606, a novel Src-Abl inhibitor, against imatinib-resistant Bcr-Abl+ neoplastic cells. Cancer Res. 2006;66:11314-11322.
-
(2006)
Cancer Res
, vol.66
, pp. 11314-11322
-
-
Puttini, M.1
Coluccia, A.M.2
Boschelli, F.3
-
12
-
-
30644462841
-
Targeted CML therapy: Controlling drug resistance, seeking cure
-
O'Hare T, Corbin AS, Druker BJ. Targeted CML therapy: controlling drug resistance, seeking cure. Curr Opin Genet Dev. 2006;16:92-99.
-
(2006)
Curr Opin Genet Dev
, vol.16
, pp. 92-99
-
-
O'Hare, T.1
Corbin, A.S.2
Druker, B.J.3
-
15
-
-
0038341158
-
The Aurora kinases: Role in cell transformation and tumori-genesis
-
Katayama H, Brinkley WR, Sen S. The Aurora kinases: role in cell transformation and tumori-genesis. Cancer Metastasis Rev. 2003;22:451-464.
-
(2003)
Cancer Metastasis Rev
, vol.22
, pp. 451-464
-
-
Katayama, H.1
Brinkley, W.R.2
Sen, S.3
-
16
-
-
23744503085
-
Aurora kinases: Shining lights on the therapeutic horizon?
-
Andrews PD. Aurora kinases: shining lights on the therapeutic horizon? Oncogene. 2005;24: 5005-5015.
-
(2005)
Oncogene
, vol.24
, pp. 5005-5015
-
-
Andrews, P.D.1
-
17
-
-
10344236486
-
Aurora-kinase inhibitors as anticancer agents
-
Keen N, Taylor S. Aurora-kinase inhibitors as anticancer agents. Nat Rev Cancer. 2004;4: 927-936.
-
(2004)
Nat Rev Cancer
, vol.4
, pp. 927-936
-
-
Keen, N.1
Taylor, S.2
-
18
-
-
2342639645
-
VX-680, a potent and selective small-molecule inhibitor of the Aurora kinases, suppresses tumor growth in vivo
-
Harrington EA, Bebbington D, Moore J, et al. VX-680, a potent and selective small-molecule inhibitor of the Aurora kinases, suppresses tumor growth in vivo. Nat Med. 2004;10:262-267.
-
(2004)
Nat Med
, vol.10
, pp. 262-267
-
-
Harrington, E.A.1
Bebbington, D.2
Moore, J.3
-
19
-
-
31644438945
-
Structure of the kinase domain of an imatinib-resistant Abl mutant in complex with the Aurora kinase inhibitor VX-680
-
Young MA, Shah NP, Chao LH, et al. Structure of the kinase domain of an imatinib-resistant Abl mutant in complex with the Aurora kinase inhibitor VX-680. Cancer Res. 2006;66:1007-1014.
-
(2006)
Cancer Res
, vol.66
, pp. 1007-1014
-
-
Young, M.A.1
Shah, N.P.2
Chao, L.H.3
-
20
-
-
33846240316
-
MK-0457, a novel kinase inhibitor, is active in patients with chronic myeloid leukemia or acute lymphocytic leukemia with the T315I BCR-ABL mutation
-
Giles FJ, Cortes J, Jones D, Bergstrom D, Kan- tarjian H, Freedman SJ. MK-0457, a novel kinase inhibitor, is active in patients with chronic myeloid leukemia or acute lymphocytic leukemia with the T315I BCR-ABL mutation. Blood. 2007;109:500-502.
-
(2007)
Blood
, vol.109
, pp. 500-502
-
-
Giles, F.J.1
Cortes, J.2
Jones, D.3
Bergstrom, D.4
Kan- tarjian, H.5
Freedman, S.J.6
-
21
-
-
33845367377
-
-
Fancelli D, Moll J, Varasi M, et al. 1,4,5,6-tetrahy- dropyrrolo[3.4-c]pyrazoles: identification of a potent Aurora kinase inhibitor with a favorable antitumor kinase inhibition profile. J Med Chem. 2006:49:7247-7251.
-
Fancelli D, Moll J, Varasi M, et al. 1,4,5,6-tetrahy- dropyrrolo[3.4-c]pyrazoles: identification of a potent Aurora kinase inhibitor with a favorable antitumor kinase inhibition profile. J Med Chem. 2006:49:7247-7251.
-
-
-
-
22
-
-
9144233483
-
Inhibitory effect of imatinib on normal progenitor cells in vitro
-
Bartolovic K, Balabanov S, Hartmann U, et al. Inhibitory effect of imatinib on normal progenitor cells in vitro. Blood. 2004;103:523-529.
-
(2004)
Blood
, vol.103
, pp. 523-529
-
-
Bartolovic, K.1
Balabanov, S.2
Hartmann, U.3
-
23
-
-
33846939244
-
Hy- pusination of eukaryotic initiation factor 5A (elF5A): A novel therapeutic target in BCR-ABL-positive leukemias identified by a proteomics approach
-
Balabanov S, Gontarewicz A, Ziegler P, et al. Hy- pusination of eukaryotic initiation factor 5A (elF5A): a novel therapeutic target in BCR-ABL-positive leukemias identified by a proteomics approach. Blood. 2007;109:1701 -1711.
-
(2007)
Blood
, vol.109
, pp. 1701-1711
-
-
Balabanov, S.1
Gontarewicz, A.2
Ziegler, P.3
-
24
-
-
61849136570
-
PHA-739358. an Aurora kinase inhibitor, induces clinical responses in chronic myeloid leukemia harboring T3151 mutations of BGR-ABL [abstract]
-
Paquette L, Shah NR Sawyers CL, et al. PHA-739358. an Aurora kinase inhibitor, induces clinical responses in chronic myeloid leukemia harboring T3151 mutations of BGR-ABL [abstract]. Blood. 2007;108(Suppl 1):1030.
-
(2007)
Blood
, vol.108
, Issue.SUPPL. 1
, pp. 1030
-
-
Paquette, L.1
Shah, N.R.2
Sawyers, C.L.3
-
25
-
-
0036090222
-
Primitive, quiescent, Philadelphia-positive stem cells from patients with chronic myeloid leukemia are insensitive to STI571 in vitro
-
Graham SM, Jorgensen HG, Allan E, et al. Primitive, quiescent, Philadelphia-positive stem cells from patients with chronic myeloid leukemia are insensitive to STI571 in vitro. Blood. 2002;99:319-325.
-
(2002)
Blood
, vol.99
, pp. 319-325
-
-
Graham, S.M.1
Jorgensen, H.G.2
Allan, E.3
-
26
-
-
33745069351
-
Bcr-Abl resistance screening predicts a limited spectrum of point mutations to be associated with clinical resistance to the Abl kinase inhibitor nilotinib (AMN107)
-
von Bubnoff N, Manley PW. Mestan J, Sanger J, Peschel G, Duyster J. Bcr-Abl resistance screening predicts a limited spectrum of point mutations to be associated with clinical resistance to the Abl kinase inhibitor nilotinib (AMN107). Blood. 2006; 108:1328-1333.
-
(2006)
Blood
, vol.108
, pp. 1328-1333
-
-
von Bubnoff, N.1
Manley, P.W.2
Mestan, J.3
Sanger, J.4
Peschel, G.5
Duyster, J.6
-
27
-
-
33749325184
-
Comparison of imatinib mesylate, dasatinib (BMS-354825), and nilotinib (AMN107) in an N-ethyl-N-nitrosourea (ENU)-based mutagenesis screen: High efficacy of drug combinations
-
Bradeen HA, Eide CA, O'Hare T, et al. Comparison of imatinib mesylate, dasatinib (BMS-354825), and nilotinib (AMN107) in an N-ethyl-N-nitrosourea (ENU)-based mutagenesis screen: high efficacy of drug combinations. Blood. 2006; 108:2332-2338.
-
(2006)
Blood
, vol.108
, pp. 2332-2338
-
-
Bradeen, H.A.1
Eide, C.A.2
O'Hare, T.3
-
28
-
-
34247615972
-
Structural basis for potent inhibition of the Aurora kinases and a T315l multi-drug resistant mutant form of Abl kinase by VX-680
-
Cheetham GM, Charlton PA, Golec JM, Pollard JR. Structural basis for potent inhibition of the Aurora kinases and a T315l multi-drug resistant mutant form of Abl kinase by VX-680. Cancer Lett. 2007;251:323-329.
-
(2007)
Cancer Lett
, vol.251
, pp. 323-329
-
-
Cheetham, G.M.1
Charlton, P.A.2
Golec, J.M.3
Pollard, J.R.4
-
29
-
-
33845285906
-
A sequential blockade strategy for the design of combination therapies to overcome oncogene addiction in chronic myelogenous leukemia
-
Chen R, Gandhi V, Plunkett W. A sequential blockade strategy for the design of combination therapies to overcome oncogene addiction in chronic myelogenous leukemia. Cancer Res. 2006;66:10959-10966.
-
(2006)
Cancer Res
, vol.66
, pp. 10959-10966
-
-
Chen, R.1
Gandhi, V.2
Plunkett, W.3
-
30
-
-
33750303818
-
Cotreat-ment with vorinostat (suberoylanilide hydroxamic acid) enhances activity of dasatinib (BMS-354825) against imatinib rnesylate-sensitive or irnatinib mesylate-resistant chronic myelogenous leukemia cells
-
Fiskus W, Pranpat M, Balasis M, et al. Cotreat-ment with vorinostat (suberoylanilide hydroxamic acid) enhances activity of dasatinib (BMS-354825) against imatinib rnesylate-sensitive or irnatinib mesylate-resistant chronic myelogenous leukemia cells. Clin Cancer Res. 2006;12:5869-5878.
-
(2006)
Clin Cancer Res
, vol.12
, pp. 5869-5878
-
-
Fiskus, W.1
Pranpat, M.2
Balasis, M.3
-
31
-
-
33745888156
-
Combined effects of novel tyrosine kinase inhibitor AMN107 and histone deacetylase inhibitor LBH589 against Bcr-Abl-expressing human leukemia cells
-
Fiskus W, Pranpat M, Bali P, et al. Combined effects of novel tyrosine kinase inhibitor AMN107 and histone deacetylase inhibitor LBH589 against Bcr-Abl-expressing human leukemia cells. Blood. 2006;108:645-652.
-
(2006)
Blood
, vol.108
, pp. 645-652
-
-
Fiskus, W.1
Pranpat, M.2
Bali, P.3
-
32
-
-
0013057087
-
Aurora B couples chromosome alignment with anaphase by targeting BubR1. Mad2. and Cenp-E to kineto- chores
-
Ditchfield C; Johnson VL, Tighe A, et al. Aurora B couples chromosome alignment with anaphase by targeting BubR1. Mad2. and Cenp-E to kineto- chores. J Cell Biol. 2003;161:267-280.
-
(2003)
J Cell Biol
, vol.161
, pp. 267-280
-
-
Ditchfield, C.1
Johnson, V.L.2
Tighe, A.3
-
33
-
-
0038746733
-
The small molecule Hesperadin reveals a role for Aurora B in correcting kinetochore-microtubule attachment and in maintaining the spindle assembly checkpoint
-
Hauf S, Cole RW, LaTerra S, et al. The small molecule Hesperadin reveals a role for Aurora B in correcting kinetochore-microtubule attachment and in maintaining the spindle assembly checkpoint. J Cell Biol. 2003;161: 281-294.
-
(2003)
J Cell Biol
, vol.161
, pp. 281-294
-
-
Hauf, S.1
Cole, R.W.2
LaTerra, S.3
-
34
-
-
34548548332
-
Crystal structure of the T3151 Abl mutant in complex with the aurora kinases inhibitor PHA-739358
-
Modugno M, Casale E, Soncini C, et al. Crystal structure of the T3151 Abl mutant in complex with the aurora kinases inhibitor PHA-739358. Cancer Res. 2007;67:7987-7990.
-
(2007)
Cancer Res
, vol.67
, pp. 7987-7990
-
-
Modugno, M.1
Casale, E.2
Soncini, C.3
|