-
1
-
-
0141465061
-
The role of FLT3 in haematopoietic malignancies
-
Stirewalt DL, Radich JP. The role of FLT3 in haematopoietic malignancies. Nat Rev Cancer 2003;3:650-65. (Pubitemid 37328820)
-
(2003)
Nature Reviews Cancer
, vol.3
, Issue.9
, pp. 650-665
-
-
Stirewalt, D.L.1
Radich, J.P.2
-
2
-
-
78650073854
-
FLT3 as a therapeutic target in AML: Still challenging after all these years
-
Kindler T, Lipka DB, Fischer T. FLT3 as a therapeutic target in AML: still challenging after all these years. Blood 2010;116:5089-102.
-
(2010)
Blood
, vol.116
, pp. 5089-5102
-
-
Kindler, T.1
Lipka, D.B.2
Fischer, T.3
-
3
-
-
0031686409
-
Internal tandem duplication of the FLT3 gene is a novel modality of elongation mutation which causes constitutive activation of the product
-
Kiyoi H, Towatari M, Yokota S, Hamaguchi M, Ohno R, Saito H, et al. Internal tandem duplication of the FLT3 gene is a novel modality of elongation mutation which causes constitutive activation of the product. Leukemia 1998;12:1333-7. (Pubitemid 28442377)
-
(1998)
Leukemia
, vol.12
, Issue.9
, pp. 1333-1337
-
-
Kiyoi, H.1
Towatari, M.2
Yokota, S.3
Hamaguchi, M.4
Ohno, R.5
Saito, H.6
Naoe, T.7
-
4
-
-
0033758958
-
FLT3 internal tandem duplication mutations in adult acute myeloid leukaemia define a high-risk group
-
Abu-Duhier FM, Goodeve AC, Wilson GA, Gari MA, Peake IR, Rees DC, et al. FLT3 internal tandem duplication mutations in adult acute myeloid leukaemia define a high-risk group. Br J Haematol 2000; 111:190-5.
-
(2000)
Br J Haematol
, vol.111
, pp. 190-195
-
-
Abu-Duhier, F.M.1
Goodeve, A.C.2
Wilson, G.A.3
Gari, M.A.4
Peake, I.R.5
Rees, D.C.6
-
5
-
-
33745198953
-
Stability and prognostic influence of FLT3 mutations in paired initial and relapsed AML samples
-
DOI 10.1038/sj.leu.2404246, PII 2404246
-
Cloos J, Goemans BF, Hess CJ, van Oostveen JW, Waisfisz Q, Corthals S, et al. Stability and prognostic influence of FLT3 mutations in paired initial and relapsed AML samples. Leukemia 2006; 20:1217-20. (Pubitemid 43905824)
-
(2006)
Leukemia
, vol.20
, Issue.7
, pp. 1217-1220
-
-
Cloos, J.1
Goemans, B.F.2
Hess, C.J.3
Van Oostveen, J.W.4
Waisfisz, Q.5
Corthals, S.6
De Lange, D.7
Boeckx, N.8
Hahlen, K.9
Reinhardt, D.10
Creutzig, U.11
Schuurhuis, G.J.12
Zwaan, Ch.M.13
Kaspers, G.J.L.14
-
6
-
-
0036720398
-
The roles of FLT3 in hematopoiesis and leukemia
-
DOI 10.1182/blood-2002-02-0492
-
Gilliland DG, Griffin JD. The roles of FLT3 in hematopoiesis and leukemia. Blood 2002;100:1532-42. (Pubitemid 34925124)
-
(2002)
Blood
, vol.100
, Issue.5
, pp. 1532-1542
-
-
Gary Gilliland, D.1
Griffin, J.D.2
-
7
-
-
0035476264
-
Absence of the wild-type allele predicts poor prognosis in adult de novo acute myeloid leukemia with normal cytogenetics and the internal tandem duplication of FLT3: A cancer and leukemia group B study
-
Whitman SP, Archer KJ, Feng L, Baldus C, Becknell B, Carlson BD, et al. Absence of the wild-type allele predicts poor prognosis in adult de novo acute myeloid leukemia with normal cytogenetics and the internal tandem duplication of FLT3: a cancer and leukemia group B study. Cancer Res 2001;61:7233-9. (Pubitemid 32946520)
-
(2001)
Cancer Research
, vol.61
, Issue.19
, pp. 7233-7239
-
-
Whitman, S.P.1
Archer, K.J.2
Feng, L.3
Baldus, C.4
Becknell, B.5
Carlson, B.D.6
Carroll, A.J.7
Mrozek, K.8
Vardiman, J.W.9
George, S.L.10
Kolitz, J.E.11
Larson, R.A.12
Bloomfield, C.D.13
Caligiuri, M.A.14
-
8
-
-
10744230464
-
Biologic and clinical significance of the FLT3 transcript level in acute myeloid leukemia
-
DOI 10.1182/blood-2003-06-1845
-
Ozeki K, Kiyoi H, Hirose Y, Iwai M, Ninomiya M, Kodera Y, et al. Biologic and clinical significance of the FLT3 transcript level in acute myeloid leukemia. Blood 2004;103:1901-8. (Pubitemid 38268989)
-
(2004)
Blood
, vol.103
, Issue.5
, pp. 1901-1908
-
-
Ozeki, K.1
Kiyoi, H.2
Hirose, Y.3
Iwai, M.4
Ninomiya, M.5
Kodera, Y.6
Miyawaki, S.7
Kuriyama, K.8
Shimazaki, C.9
Akiyama, H.10
Nishimura, M.11
Motoji, T.12
Shinagawa, K.13
Takeshita, A.14
Ueda, R.15
Ohno, R.16
Emi, N.17
Naoe, T.18
-
9
-
-
27544450742
-
Constitutive activation of Akt by Flt3 internal tandem duplications is necessary for increased survival, proliferation, and myeloid transformation
-
DOI 10.1158/0008-5472.CAN-05-0422
-
Brandts CH, Sargin B, Rode M, Biermann C, Lindtner B, Schwable J, et al. Constitutive activation of Akt by Flt3 internal tandem duplications is necessary for increased survival, proliferation, and myeloid transformation. Cancer Res 2005;65:9643-50. (Pubitemid 41541439)
-
(2005)
Cancer Research
, vol.65
, Issue.21
, pp. 9643-9650
-
-
Brandts, C.H.1
Sargin, B.2
Rode, M.3
Biermann, C.4
Lindtner, B.5
Schwable, J.6
Buerger, H.7
Muller-Tidow, C.8
Choudhary, C.9
McMahon, M.10
Berdel, W.E.11
Serve, H.12
-
10
-
-
34347401419
-
Activation mechanisms of STAT5 by oncogenic Flt3-ITD
-
DOI 10.1182/blood-2006-05-024018
-
Choudhary C, Brandts C, Schwable J, Tickenbrock L, Sargin B, Ueker A, et al. Activation mechanisms of STAT5 by oncogenic Flt3-ITD. Blood 2007;110:370-4. (Pubitemid 47026856)
-
(2007)
Blood
, vol.110
, Issue.1
, pp. 370-374
-
-
Choudhary, C.1
Brandts, C.2
Schwable, J.3
Tickenbrock, L.4
Sargin, B.5
Ueker, A.6
Bohmer, F.-D.7
Berdel, W.E.8
Muller-Tidow, C.9
Serve, H.10
-
11
-
-
0034598830
-
Tandem-duplicated Flt3 constitutively activates STAT5 and MAP kinase and introduces autonomous cell growth in IL-3-dependent cell lines
-
Hayakawa F, Towatari M, Kiyoi H, Tanimoto M, Kitamura T, Saito H, et al. Tandem-duplicated Flt3 constitutively activates STAT5 and MAP kinase and introduces autonomous cell growth in IL-3-dependent cell lines. Oncogene 2000;19:624-31. (Pubitemid 30102913)
-
(2000)
Oncogene
, vol.19
, Issue.5
, pp. 624-631
-
-
Hayakawa, F.1
Towatari, M.2
Kiyoi, H.3
Tanimoto, M.4
Kitamura, T.5
Saito, H.6
Naoe, T.7
-
12
-
-
0034554796
-
Flt3 mutations from patients with acute myeloid leukemia induce transformation of 32D cells mediated by the Ras and STAT5 pathways
-
Mizuki M, Fenski R, Halfter H, Matsumura I, Schmidt R, Muller C, et al. Flt3 mutations from patients with acute myeloid leukemia induce transformation of 32D cells mediated by the Ras and STAT5 pathways. Blood 2000;96:3907-14.
-
(2000)
Blood
, vol.96
, pp. 3907-3914
-
-
Mizuki, M.1
Fenski, R.2
Halfter, H.3
Matsumura, I.4
Schmidt, R.5
Muller, C.6
-
13
-
-
33747189188
-
Roles of tyrosine 589 and 591 in STAT5 activation and transformation mediated by FLT3-ITD
-
DOI 10.1182/blood-2005-11-011429
-
Rocnik JL, Okabe R, Yu JC, Lee BH, Giese N, Schenkein DP, et al. Roles of tyrosine 589 and 591 in STAT5 activation and transformation mediated by FLT3-ITD. Blood 2006;108:1339-45. (Pubitemid 44232034)
-
(2006)
Blood
, vol.108
, Issue.4
, pp. 1339-1345
-
-
Rocnik, J.L.1
Okabe, R.2
Yu, J.-C.3
Lee, B.H.4
Giese, N.5
Schenkein, D.P.6
Gilliland, D.G.7
-
15
-
-
33845240584
-
Phase 1 clinical results with tandutinib (MLN518), a novel FLT3 antagonist, in patients with acute myelogenous leukemia or high-risk myelodysplastic syndrome: Safety, pharmacokinetics, and pharmacodynamics
-
DOI 10.1182/blood-2006-02-005702
-
DeAngelo DJ, Stone RM, Heaney ML, Nimer SD, Paquette RL, Klisovic RB, et al. Phase 1 clinical results with tandutinib (MLN518), a novel FLT3 antagonist, in patients with acute myelogenous leukemia or high-risk myelodysplastic syndrome: safety, pharmacokinetics, and phar-macodynamics. Blood 2006;108:3674-81. (Pubitemid 44864544)
-
(2006)
Blood
, vol.108
, Issue.12
, pp. 3674-3681
-
-
DeAngelo, D.J.1
Stone, R.M.2
Heaney, M.L.3
Nimer, S.D.4
Paquette, R.L.5
Klisovic, R.B.6
Caligiuri, M.A.7
Cooper, M.R.8
Lecerf, J.-M.9
Karol, M.D.10
Sheng, S.11
Holford, N.12
Curtin, P.T.13
Druker, B.J.14
Heinrich, M.C.15
-
16
-
-
19944431093
-
A phase 1 study of SU11248 in the treatment of patients with refractory or resistant acute myeloid leukemia (AML) or not amenable to conventional therapy for the disease
-
DOI 10.1182/blood-2004-05-1846
-
Fiedler W, Serve H, Dohner H, Schwittay M, Ottmann OG, O'Farrell AM, et al. A phase 1 study of SU11248 in the treatment of patients with refractory or resistant acute myeloid leukemia (AML) or not amenable to conventional therapy for the disease. Blood 2005;105:986-93. (Pubitemid 40170865)
-
(2005)
Blood
, vol.105
, Issue.3
, pp. 986-993
-
-
Fiedler, W.1
Serve, H.2
Dohner, H.3
Schwittay, M.4
Ottmann, O.G.5
O'Farrell, A.-M.6
Bello, C.L.7
Allred, R.8
Manning, W.C.9
Cherrington, J.M.10
Louie, S.G.11
Hong, W.12
Brega, N.M.13
Massimini, G.14
Scigalla, P.15
Berdel, W.E.16
Hossfeld, D.K.17
-
17
-
-
33751173636
-
A phase 2 trial of the FLT3 inhibitor lestaurtinib (CEP701) as firstline treatment for older patients with acute myeloid leukemia not considered fit for intensive chemotherapy
-
Knapper S, Burnett AK, Littlewood T, Kell WJ, Agrawal S, Chopra R, et al. A phase 2 trial of the FLT3 inhibitor lestaurtinib (CEP701) as firstline treatment for older patients with acute myeloid leukemia not considered fit for intensive chemotherapy. Blood 2006;108:3262-70.
-
(2006)
Blood
, vol.108
, pp. 3262-3270
-
-
Knapper, S.1
Burnett, A.K.2
Littlewood, T.3
Kell, W.J.4
Agrawal, S.5
Chopra, R.6
-
18
-
-
0038204144
-
SU11248 is a novel FLT3 tyrosine kinase inhibitor with potent activity in vitro and in vivo
-
DOI 10.1182/blood-2002-07-2307
-
O'Farrell AM, Abrams TJ, Yuen HA, Ngai TJ, Louie SG, Yee KW, et al. SU11248 is a novel FLT3 tyrosine kinase inhibitor with potent activity in vitro and in vivo. Blood 2003;101:3597-605. (Pubitemid 36857948)
-
(2003)
Blood
, vol.101
, Issue.9
, pp. 3597-3605
-
-
O'Farrell, A.-M.1
Abrams, T.J.2
Yuen, H.A.3
Ngai, T.J.4
Louie, S.G.5
Yee, K.W.H.6
Wong, L.M.7
Hong, W.8
Lee, L.B.9
Town, A.10
Smolich, B.D.11
Manning, W.C.12
Murray, L.J.13
Heinrich, M.C.14
Cherrington, J.M.15
-
19
-
-
0345359585
-
An innovative phase i clinical study demonstrates inhibition of FLT3 phosphorylation by SU11248 in acute myeloid leukemia patients
-
O'Farrell AM, Foran JM, Fiedler W, Serve H, Paquette RL, Cooper MA, et al. An innovative phase I clinical study demonstrates inhibition of FLT3 phosphorylation by SU11248 in acute myeloid leukemia patients. Clin Cancer Res 2003;9:5465-76. (Pubitemid 37499464)
-
(2003)
Clinical Cancer Research
, vol.9
, Issue.15
, pp. 5465-5476
-
-
O'Farrell, A.-M.1
Foran, J.M.2
Fiedler, W.3
Serve, H.4
Paquette, R.L.5
Cooper, M.A.6
Yuen, H.A.7
Louie, S.G.8
Kim, H.9
Nicholas, S.10
Heinrich, M.C.11
Berdel, W.E.12
Bello, C.13
Jacobs, M.14
Scigalla, P.15
Manning, W.C.16
Kelsey, S.17
Cherrington, J.M.18
-
20
-
-
1842420032
-
Single-agent CEP-701, a novel FLT3 inhibitor, shows biologic and clinical activity in patients with relapsed or refractory acute myeloid leukemia
-
DOI 10.1182/blood-2003-11-3775
-
Smith BD, Levis M, Beran M, Giles F, Kantarjian H, Berg K, et al. Singleagent CEP-701, a novel FLT3 inhibitor, shows biologic and clinical activity in patients with relapsed or refractory acute myeloid leukemia. Blood 2004;103:3669-76. (Pubitemid 38596280)
-
(2004)
Blood
, vol.103
, Issue.10
, pp. 3669-3676
-
-
Smith, B.D.1
Levis, M.2
Beran, M.3
Giles, F.4
Kantarjian, H.5
Berg, K.6
Murphy, K.M.7
Dauses, T.8
Allebach, J.9
Small, D.10
-
21
-
-
19944427559
-
Patients with acute myeloid leukemia and an activating mutation in FLT3 respond to a small-molecule FLT3 tyrosine kinase inhibitor, PKC412
-
DOI 10.1182/blood-2004-03-0891
-
Stone RM, DeAngelo DJ, Klimek V, Galinsky I, Estey E, Nimer SD, et al. Patients with acute myeloid leukemia and an activating mutation in FLT3 respond to a small-molecule FLT3 tyrosine kinase inhibitor, PKC412. Blood 2005;105:54-60. (Pubitemid 40053063)
-
(2005)
Blood
, vol.105
, Issue.1
, pp. 54-60
-
-
Stone, R.M.1
DeAngelo, D.J.2
Klimek, V.3
Galinsky, I.4
Estey, E.5
Nimer, S.D.6
Grandin, W.7
Lebwohl, D.8
Wang, Y.9
Cohen, P.10
Fox, E.A.11
Neuberg, D.12
Clark, J.13
Gilliland, D.G.14
Griffin, J.D.15
-
22
-
-
77954494236
-
FLT3 inhibitors for the treatment of acute myeloid leukemia
-
Wiernik PH. FLT3 inhibitors for the treatment of acute myeloid leukemia. Clin Adv Hematol Oncol 2010;8:429-44.
-
(2010)
Clin Adv Hematol Oncol
, vol.8
, pp. 429-444
-
-
Wiernik, P.H.1
-
23
-
-
33847195060
-
Antitumor activity of sorafenib in FLT3-driven leukemic cells
-
Auclair D, Miller D, Yatsula V, Pickett W, Carter C, Chang Y, et al. Antitumor activity of sorafenib in FLT3-driven leukemic cells. Leukemia 2007;21:439-45.
-
(2007)
Leukemia
, vol.21
, pp. 439-445
-
-
Auclair, D.1
Miller, D.2
Yatsula, V.3
Pickett, W.4
Carter, C.5
Chang, Y.6
-
24
-
-
0013102301
-
CT53518, a novel selective FLT3 antagonist for the treatment of acute myelogenous leukemia (AML)
-
DOI 10.1016/S1535-6108(02)00070-3
-
Kelly LM, Yu JC, Boulton CL, Apatira M, Li J, Sullivan CM, et al. CT53518, a novel selective FLT3 antagonist for the treatment of acute myelogenous leukemia (AML). Cancer Cell 2002;1:421-32. (Pubitemid 41039123)
-
(2002)
Cancer Cell
, vol.1
, Issue.5
, pp. 421-432
-
-
Kelly, L.M.1
Yu, J.-C.2
Boulton, C.L.3
Apatira, M.4
Li, J.5
Sullivan, C.M.6
Williams, I.7
Amaral, S.M.8
Curley, D.P.9
Duclos, N.10
Neuberg, D.11
Scarborough, R.M.12
Pandey, A.13
Hollenbach, S.14
Abe, K.15
Lokker, N.A.16
Gilliland, D.G.17
Giese, N.A.18
-
25
-
-
0036624916
-
A FLT3-targeted tyrosine kinase inhibitor is cytotoxic to leukemia cells in vitro and in vivo
-
DOI 10.1182/blood.V99.11.3885
-
Levis M, Allebach J, Tse KF, Zheng R, Baldwin BR, Smith BD, et al. A FLT3-targeted tyrosine kinase inhibitor is cytotoxic to leukemia cells in vitro and in vivo. Blood 2002;99:3885-91. (Pubitemid 35332023)
-
(2002)
Blood
, vol.99
, Issue.11
, pp. 3885-3891
-
-
Levis, M.1
Allebach, J.2
Tse, K.-F.3
Zheng, R.4
Brenda, R.5
Baldwin, B.6
Smith, D.7
Jones-Bolin, S.8
Ruggeri, B.9
Dionne, C.10
Small, D.11
-
26
-
-
62949087552
-
A pharmacodynamic study of the FLT3 inhibitor KW-2449 yields insight into the basis for clinical response
-
Pratz KW, Cortes J, Roboz GJ, Rao N, Arowojolu O, Stine A, et al. A pharmacodynamic study of the FLT3 inhibitor KW-2449 yields insight into the basis for clinical response. Blood 2009;113:3938-46.
-
(2009)
Blood
, vol.113
, pp. 3938-3946
-
-
Pratz, K.W.1
Cortes, J.2
Roboz, G.J.3
Rao, N.4
Arowojolu, O.5
Stine, A.6
-
27
-
-
34147102941
-
ABT-869, a multitargeted receptor tyrosine kinase inhibitor: Inhibition of FLT3 phosphorylation and signaling in acute myeloid leukemia
-
DOI 10.1182/blood-2006-06-029579
-
Shankar DB, Li J, Tapang P, Owen McCall J, Pease LJ, Dai Y, et al. ABT-869, a multitargeted receptor tyrosine kinase inhibitor: inhibition of FLT3 phosphorylation and signaling in acute myeloid leukemia. Blood 2007;109:3400-8. (Pubitemid 46572529)
-
(2007)
Blood
, vol.109
, Issue.8
, pp. 3400-3408
-
-
Shankar, D.B.1
Li, J.2
Tapang, P.3
McCall, J.O.4
Pease, L.J.5
Dai, Y.6
Wei, R.-Q.7
Albert, D.H.8
Bouska, J.J.9
Osterling, D.J.10
Guo, J.11
Marcotte, P.A.12
Johnson, E.F.13
Soni, N.14
Hartandi, K.15
Michaelides, M.R.16
Davidsen, S.K.17
Priceman, S.J.18
Chang, J.C.19
Rhodes, K.20
Shah, N.21
Moore, T.B.22
Sakamoto, K.M.23
Glaser, K.B.24
more..
-
28
-
-
0036595143
-
Inhibition of mutant FLT3 receptors in leukemia cells by the small molecule tyrosine kinase inhibitor PKC412
-
DOI 10.1016/S1535-6108(02)00069-7
-
Weisberg E, Boulton C, Kelly LM, Manley P, Fabbro D, Meyer T, et al. Inhibition of mutant FLT3 receptors in leukemia cells by the small molecule tyrosine kinase inhibitor PKC412. Cancer Cell 2002;1: 433-43. (Pubitemid 41039124)
-
(2002)
Cancer Cell
, vol.1
, Issue.5
, pp. 433-443
-
-
Weisberg, E.1
Boulton, C.2
Kelly, L.M.3
Manley, P.4
Fabbro, D.5
Meyer, T.6
Gilliland, D.G.7
Griffin, J.D.8
-
29
-
-
77954750384
-
Bench to bedside targeting of FLT3 in acute leukemia
-
Pratz KW, Levis MJ. Bench to bedside targeting of FLT3 in acute leukemia. Curr Drug Targets 2010;11:781-9.
-
(2010)
Curr Drug Targets
, vol.11
, pp. 781-789
-
-
Pratz, K.W.1
Levis, M.J.2
-
30
-
-
70449475105
-
AC220 is a uniquely potent and selective inhibitor of FLT3 for the treatment of acute myeloid leukemia (AML)
-
Zarrinkar PP, Gunawardane RN, Cramer MD, Gardner MF, Brigham D, Belli B, et al. AC220 is a uniquely potent and selective inhibitor of FLT3 for the treatment of acute myeloid leukemia (AML). Blood 2009;114: 2984-92.
-
(2009)
Blood
, vol.114
, pp. 2984-2992
-
-
Zarrinkar, P.P.1
Gunawardane, R.N.2
Cramer, M.D.3
Gardner, M.F.4
Brigham, D.5
Belli, B.6
-
31
-
-
33751170444
-
Plasma inhibitory activity (PIA): A pharmacodynamic assay reveals insights into the basis for cytotoxic response to FLT3 inhibitors
-
Levis M, Brown P, Smith BD, Stine A, Pham R, Stone R, et al. Plasma inhibitory activity (PIA): a pharmacodynamic assay reveals insights into the basis for cytotoxic response to FLT3 inhibitors. Blood 2006;108: 3477-83.
-
(2006)
Blood
, vol.108
, pp. 3477-3483
-
-
Levis, M.1
Brown, P.2
Smith, B.D.3
Stine, A.4
Pham, R.5
Stone, R.6
-
32
-
-
39149129114
-
Mutant FLT3: A direct target of sorafenib in acute myelogenous leukemia
-
DOI 10.1093/jnci/djm328
-
Zhang W, Konopleva M, Shi YX, McQueen T, Harris D, Ling X, et al. Mutant FLT3: a direct target of sorafenib in acute myelogenous leukemia. J Natl Cancer Inst 2008;100:184-98. (Pubitemid 351480557)
-
(2008)
Journal of the National Cancer Institute
, vol.100
, Issue.3
, pp. 184-198
-
-
Zhang, W.1
Konopleva, M.2
Shi, Y.-X.3
McQueen, T.4
Harris, D.5
Ling, X.6
Estrov, Z.7
Quintas-Cardama, A.8
Small, D.9
Cortes, J.10
Andreeff, M.11
-
33
-
-
78649340278
-
Activation state-dependent binding of small molecule kinase inhibitors: Structural insights from biochemistry
-
Wodicka LM, Ciceri P, Davis MI, Hunt JP, Floyd M, Salerno S, et al. Activation state-dependent binding of small molecule kinase inhibitors: structural insights from biochemistry. Chem Biol 2010;17: 1241-9.
-
(2010)
Chem Biol
, vol.17
, pp. 1241-1249
-
-
Wodicka, L.M.1
Ciceri, P.2
Davis, M.I.3
Hunt, J.P.4
Floyd, M.5
Salerno, S.6
-
34
-
-
0026425674
-
Experimental antitumor activity of taxotere (RP 56976, NSC 628503), a taxol analogue
-
Bissery MC, Guenard D, Gueritte-Voegelein F, Lavelle F. Experimental antitumor activity of taxotere (RP 56976, NSC 628503), a taxol analogue. Cancer Res 1991;51:4845-52.
-
(1991)
Cancer Res
, vol.51
, pp. 4845-4852
-
-
Bissery, M.C.1
Guenard, D.2
Gueritte-Voegelein, F.3
Lavelle, F.4
-
35
-
-
0037265645
-
FLT3 mutations in acute myeloid leukemia cell lines
-
DOI 10.1038/sj.leu.2402740
-
Quentmeier H, Reinhardt J, Zaborski M, Drexler HG. FLT3 mutations in acute myeloid leukemia cell lines. Leukemia 2003;17:120-4. (Pubitemid 36175896)
-
(2003)
Leukemia
, vol.17
, Issue.1
, pp. 120-124
-
-
Quentmeier, H.1
Reinhardt, J.2
Zaborski, M.3
Drexler, H.G.4
-
36
-
-
0037838661
-
Overexpression and constitutive activation of FLT3 induces STAT5 activation in primary acute myeloid leukemia blast cells
-
Spiekermann K, Bagrintseva K, Schwab R, Schmieja K, Hiddemann W. Overexpression and constitutive activation of FLT3 induces STAT5 activation in primary acute myeloid leukemia blast cells. Clin Cancer Res 2003;9:2140-50. (Pubitemid 36687636)
-
(2003)
Clinical Cancer Research
, vol.9
, Issue.6
, pp. 2140-2150
-
-
Spiekermann, K.1
Bagrintseva, K.2
Schwab, R.3
Schmieja, K.4
Hiddemann, W.5
-
37
-
-
33846930383
-
The ability of sorafenib to inhibit oncogenic PDGFRβ and FLT3 mutants and overcome resistance to other small molecule inhibitors
-
DOI 10.3324/haematol.10692
-
Lierman E, Lahortiga I, Van Miegroet H, Mentens N, Marynen P, Cools J. The ability of sorafenib to inhibit oncogenic PDGFRbeta and FLT3 mutants and overcome resistance to other small molecule inhibitors. Haematologica 2007;92:27-34. (Pubitemid 46232655)
-
(2007)
Haematologica
, vol.92
, Issue.1
, pp. 27-34
-
-
Lierman, E.1
Lahortiga, I.2
Van Miegroet, H.3
Mentens, N.4
Marynen, P.5
Cools, J.6
-
38
-
-
4444342401
-
Pediatric AML primary samples with FLT3/ITD mutations are preferentially killed by FLT3 inhibition
-
DOI 10.1182/blood-2004-03-1034
-
Brown P, Meshinchi S, Levis M, Alonzo TA, Gerbing R, Lange B, et al. Pediatric AML primary samples with FLT3/ITD mutations are preferentially killed by FLT3 inhibition. Blood 2004;104:1841-9. (Pubitemid 39202295)
-
(2004)
Blood
, vol.104
, Issue.6
, pp. 1841-1849
-
-
Brown, P.1
Meshinchi, S.2
Levis, M.3
Alonzo, T.A.4
Gerbing, R.5
Lange, B.6
Arceci, R.7
Small, D.8
-
39
-
-
0035437140
-
A FLT3 tyrosine kinase inhibitor is selectively cytotoxic to acute myeloid leukemia blasts harboring FLT3 internal tandem duplication mutations
-
Levis M, Tse KF, Smith BD, Garrett E, Small D. A FLT3 tyrosine kinase inhibitor is selectively cytotoxic to acute myeloid leukemia blasts harboring FLT3 internal tandem duplication mutations. Blood 2001;98:885-7.
-
(2001)
Blood
, vol.98
, pp. 885-887
-
-
Levis, M.1
Tse, K.F.2
Smith, B.D.3
Garrett, E.4
Small, D.5
-
40
-
-
78650967539
-
Phase i dose escalation trial of sorafenib as a single agent for adults with relapsed and refractory acute leukemias
-
abstr 7065
-
Pratz KW, Cho E, Karp JE, Levis M, Zhao M, Rudek M, et al. Phase I dose escalation trial of sorafenib as a single agent for adults with relapsed and refractory acute leukemias. J Clin Oncol 2009;27:abstr 7065.
-
(2009)
J Clin Oncol
, vol.27
-
-
Pratz, K.W.1
Cho, E.2
Karp, J.E.3
Levis, M.4
Zhao, M.5
Rudek, M.6
-
41
-
-
56949083913
-
Sorafenib (Nexavar) induces molecular remission and regression of extramedullary disease in a patient with FLT3-ITD acute myeloid leukemia
-
Safaian NN, Czibere A, Bruns I, Fenk R, Reinecke P, Dienst A, et al. Sorafenib (Nexavar) induces molecular remission and regression of extramedullary disease in a patient with FLT3-ITD acute myeloid leukemia. Leuk Res 2009;33:348-50.
-
(2009)
Leuk Res
, vol.33
, pp. 348-350
-
-
Safaian, N.N.1
Czibere, A.2
Bruns, I.3
Fenk, R.4
Reinecke, P.5
Dienst, A.6
-
42
-
-
70350727160
-
Acute dasatinib exposure commits Bcr-Abl-dependent cells to apo-ptosis
-
Snead JL, O'Hare T, Adrian LT, Eide CA, Lange T, Druker BJ, et al. Acute dasatinib exposure commits Bcr-Abl-dependent cells to apo-ptosis. Blood 2009;114:3459-63.
-
(2009)
Blood
, vol.114
, pp. 3459-3463
-
-
Snead, J.L.1
O'Hare, T.2
Adrian, L.T.3
Eide, C.A.4
Lange, T.5
Druker, B.J.6
-
43
-
-
4644289313
-
A unique structure for epidermal growth factor receptor bound to GW572016 (Lapatinib): Relationships among protein conformation, inhibitor off-rate, and receptor activity in tumor cells
-
DOI 10.1158/0008-5472.CAN-04-1168
-
Wood ER, Truesdale AT, McDonald AB, Derek Y, Hassell A, Dickerson SH, et al. A unique structure for epidermal growth factor receptor bound to GW572016(Lapatinib): relationships among protein conformation, inhibitor off-rate, and receptor activity in tumor cells. Cancer Res 2004;64:6652-9 (Pubitemid 39297926)
-
(2004)
Cancer Research
, vol.64
, Issue.18
, pp. 6652-6659
-
-
Wood, E.R.1
Truesdale, A.T.2
McDonald, O.B.3
Yuan, D.4
Hassell, A.5
Dickerson, S.H.6
Ellis, B.7
Pennisi, C.8
Horne, E.9
Lackey, K.10
Alligood, K.J.11
Rusnak, D.W.12
Gilmer, T.M.13
Shewchuk, L.14
-
44
-
-
77949887020
-
FLT3-mutant allelic burden and clinical status are predictive of response to FLT3 inhibitors in AML
-
Pratz KW, Sato T, Murphy KM, Stine A, Rajkhowa T, Levis M. FLT3-mutant allelic burden and clinical status are predictive of response to FLT3 inhibitors in AML. Blood 2010;115:1425-32.
-
(2010)
Blood
, vol.115
, pp. 1425-1432
-
-
Pratz, K.W.1
Sato, T.2
Murphy, K.M.3
Stine, A.4
Rajkhowa, T.5
Levis, M.6
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