-
1
-
-
33751267902
-
Acute myeloid leukaemia
-
Estey E, Dohner H. Acute myeloid leukaemia. Lancet. 2006;368(9550):1894- 1907.
-
(2006)
Lancet
, vol.368
, Issue.9550
, pp. 1894-1907
-
-
Estey, E.1
Dohner, H.2
-
2
-
-
0141465061
-
The role of FLT3 in haematopoietic malignancies
-
Stirewalt DL, Radich JP. The role of FLT3 in haematopoietic malignancies. Nat Rev Cancer. 2003;3(9):650-665.
-
(2003)
Nat Rev Cancer
, vol.3
, Issue.9
, pp. 650-665
-
-
Stirewalt, D.L.1
Radich, J.P.2
-
3
-
-
9044233643
-
Expression and signal transduction of the FLT3 tyrosine kinase receptor
-
Rosnet O, Buhring HJ, deLapeyriere O, et al. Expression and signal transduction of the FLT3 tyrosine kinase receptor. Acta Haematol. 1996; 95(3-4):218-223.
-
(1996)
Acta Haematol
, vol.95
, Issue.3-4
, pp. 218-223
-
-
Rosnet, O.1
Buhring, H.J.2
DeLapeyriere, O.3
-
4
-
-
0029134556
-
Multi-level effects of flt3 ligand on human hematopoiesis: Expansion of putative stem cells and proliferation of granulomonocytic progenitors/ monocytic precursors
-
Gabbianelli M, Pelosi E, Montesoro E, et al. Multi-level effects of flt3 ligand on human hematopoiesis: expansion of putative stem cells and proliferation of granulomonocytic progenitors/ monocytic precursors. Blood. 1995;86(5):1661-1670.
-
(1995)
Blood
, vol.86
, Issue.5
, pp. 1661-1670
-
-
Gabbianelli, M.1
Pelosi, E.2
Montesoro, E.3
-
5
-
-
0030059543
-
The FLT3 ligand is a direct and potent stimulator of the growth of primitive and committed human CD34+ bone marrow progenitor cells in vitro
-
Rusten LS, Lyman SD, Veiby OP, Jacobsen SE. The FLT3 ligand is a direct and potent stimulator of the growth of primitive and committed human CD34+ bone marrow progenitor cells in vitro. Blood. 1996;87(4):1317-1325.
-
(1996)
Blood
, vol.87
, Issue.4
, pp. 1317-1325
-
-
Rusten, L.S.1
Lyman, S.D.2
Veiby, O.P.3
Jacobsen, S.E.4
-
6
-
-
0030005639
-
- cells and maintains progenitor cells in vitro
-
Shah AJ, Smogorzewska EM, Hannum C, Crooks GM. Flt3 ligand induces proliferation of quiescent human bone marrow CD34+CD38- cells and maintains progenitor cells in vitro. Blood. 1996; 87(9):3563-3570. (Pubitemid 26129582)
-
(1996)
Blood
, vol.87
, Issue.9
, pp. 3563-3570
-
-
Shah, A.J.1
Smogorzewska, E.M.2
Hannum, A.C.3
Crooks, G.M.4
-
7
-
-
0041743233
-
Human CD34+ hematopoietic stem cells capable of multilineage engrafting NOD/SCID mice express flt3: Distinct flt3 and c-kit expression and response patterns on mouse and candidate human hematopoietic stem cells
-
Sitnicka E, Buza-Vidas N, Larsson S, Nygren JM, Liuba K, Jacobsen SE. Human CD34+ hematopoietic stem cells capable of multilineage engrafting NOD/SCID mice express flt3: distinct flt3 and c-kit expression and response patterns on mouse and candidate human hematopoietic stem cells. Blood. 2003;102(3):881-886.
-
(2003)
Blood
, vol.102
, Issue.3
, pp. 881-886
-
-
Sitnicka, E.1
Buza-Vidas, N.2
Larsson, S.3
Nygren, J.M.4
Liuba, K.5
Jacobsen, S.E.6
-
8
-
-
13344282746
-
Expression of the hematopoietic growth factor receptor FLT3 (STK-1/Flk2) in human leukemias
-
Carow CE, Levenstein M, Kaufmann SH, et al. Expression of the hematopoietic growth factor receptor FLT3 (STK-1/Flk2) in human leukemias. Blood. 1996;87(3):1089-1096.
-
(1996)
Blood
, vol.87
, Issue.3
, pp. 1089-1096
-
-
Carow, C.E.1
Levenstein, M.2
Kaufmann, S.H.3
-
9
-
-
9244260192
-
Human FLT3/FLK2 receptor tyrosine kinase is expressed at the surface of normal and malignant hematopoietic cells
-
Rosnet O, Buhring HJ, Marchetto S, et al. Human FLT3/FLK2 receptor tyrosine kinase is expressed at the surface of normal and malignant hematopoietic cells. Leukemia. 1996;10(2):238-248.
-
(1996)
Leukemia
, vol.10
, Issue.2
, pp. 238-248
-
-
Rosnet, O.1
Buhring, H.J.2
Marchetto, S.3
-
10
-
-
1542276560
-
FLT3 mutations in childhood acute lymphoblastic leukemia
-
DOI 10.1182/blood-2003-07-2441
-
Armstrong SA, Mabon ME, Silverman LB, et al. FLT3 mutations in childhood acute lymphoblastic leukemia. Blood. 2004;103(9):3544-3546. (Pubitemid 38525690)
-
(2004)
Blood
, vol.103
, Issue.9
, pp. 3544-3546
-
-
Armstrong, S.A.1
Mabon, M.E.2
Silverman, L.B.3
Li, A.4
Gribben, J.G.5
Fox, E.A.6
Sallan, S.E.7
Korsmeyer, S.J.8
-
11
-
-
0030451722
-
Internal tandem duplication of the flt3 gene found in acute myeloid leukemia
-
Nakao M, Yokota S, Iwai T, et al. Internal tandem duplication of the flt3 gene found in acute myeloid leukemia. Leukemia. 1996;10(12):1911-1918.
-
(1996)
Leukemia
, vol.10
, Issue.12
, pp. 1911-1918
-
-
Nakao, M.1
Yokota, S.2
Iwai, T.3
-
12
-
-
0037114829
-
Prognostic significance of activating FLT3 mutations in younger adults (16 to 60 years) with acute myeloid leukemia and normal cytogenetics: A study of the AML study group Ulm
-
DOI 10.1182/blood-2002-05-1440
-
Frohling S, Schlenk RF, Breitruck J, et al. Prognostic significance of activating FLT3 mutations in younger adults (16 to 60 years) with acute myeloid leukemia and normal cytogenetics: a study of the AML Study Group Ulm. Blood. 2002;100(13): 4372-4380. (Pubitemid 35434129)
-
(2002)
Blood
, vol.100
, Issue.13
, pp. 4372-4380
-
-
Frohling, S.1
Schlenk, R.F.2
Breitruck, J.3
Benner, A.4
Kreitmeier, S.5
Tobis, K.6
Dohner, H.7
Dohner, K.8
-
13
-
-
0035885955
-
The presence of a FLT3 internal tandem duplication in patients with acute myeloid leukemia (AML) adds important prognostic information to cytogenetic risk group and response to the first cycle of chemotherapy: Analysis of 854 patients from the United Kingdom Medical Research Council AML 10 and 12 trials
-
Kottaridis PD, Gale RE, Frew ME, et al. The presence of a FLT3 internal tandem duplication in patients with acute myeloid leukemia (AML) adds important prognostic information to cytogenetic risk group and response to the first cycle of chemotherapy: analysis of 854 patients from the United Kingdom Medical Research Council AML 10 and 12 trials. Blood. 2001;98(6):1752-1759.
-
(2001)
Blood
, vol.98
, Issue.6
, pp. 1752-1759
-
-
Kottaridis, P.D.1
Gale, R.E.2
Frew, M.E.3
-
14
-
-
0036659931
-
Analysis of FLT3 length mutations in 1003 patients with acute myeloid leukemia: Correlation to cytogenetics, FAB subtype, and prognosis in the AMLCG study and usefulness as a marker for the detection of minimal residual disease
-
Schnittger S, Schoch C, Dugas M, et al. Analysis of FLT3 length mutations in 1003 patients with acute myeloid leukemia: correlation to cytogenetics, FAB subtype, and prognosis in the AMLCG study and usefulness as a marker for the detection of minimal residual disease. Blood. 2002; 100(1):59-66.
-
(2002)
Blood
, vol.100
, Issue.1
, pp. 59-66
-
-
Schnittger, S.1
Schoch, C.2
Dugas, M.3
-
15
-
-
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, 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(19):7233-7239.
-
(2001)
Cancer Res
, vol.61
, Issue.19
, pp. 7233-7239
-
-
Whitman, S.P.1
Archer, K.J.2
Feng, L.3
-
16
-
-
0033134792
-
Prognostic implication of FLT3 and N-RAS gene mutations in acute myeloid leukemia
-
Kiyoi H, Naoe T, Nakano Y, et al. Prognostic implication of FLT3 and N-RAS gene mutations in acute myeloid leukemia. Blood. 1999;93(9):3074-3080.
-
(1999)
Blood
, vol.93
, Issue.9
, pp. 3074-3080
-
-
Kiyoi, H.1
Naoe, T.2
Nakano, Y.3
-
17
-
-
65449180371
-
Identification of a novel type of ITD mutations located in nonjuxtamembrane domains of the FLT3 tyrosine kinase receptor
-
Breitenbuecher F, Schnittger S, Grundler R, et al. Identification of a novel type of ITD mutations located in nonjuxtamembrane domains of the FLT3 tyrosine kinase receptor. Blood. 2009;113(17): 4074-4077.
-
(2009)
Blood
, vol.113
, Issue.17
, pp. 4074-4077
-
-
Breitenbuecher, F.1
Schnittger, S.2
Grundler, R.3
-
18
-
-
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, 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(12): 3907-3914.
-
(2000)
Blood
, vol.96
, Issue.12
, pp. 3907-3914
-
-
Mizuki, M.1
Fenski, R.2
Halfter, H.3
-
19
-
-
27544450742
-
Constitutive activation of Akt by Flt3 internal tandem duplications is necessary for increased survival, proliferation, and myeloid transformation
-
Brandts CH, Sargin B, Rode M, et al. Constitutive activation of Akt by Flt3 internal tandem duplications is necessary for increased survival, proliferation, and myeloid transformation. Cancer Res. 2005;65(21):9643-9650.
-
(2005)
Cancer Res
, vol.65
, Issue.21
, pp. 9643-9650
-
-
Brandts, C.H.1
Sargin, B.2
Rode, M.3
-
20
-
-
0036093475
-
FLT3 internal tandem duplication mutations associated with human acute myeloid leukemias induce myeloproliferative disease in a murine bone marrow transplant model
-
Kelly LM, Liu Q, Kutok JL, Williams IR, Boulton CL, Gilliland DG. FLT3 internal tandem duplication mutations associated with human acute myeloid leukemias induce myeloproliferative disease in a murine bone marrow transplant model. Blood. 2002;99(1):310-318.
-
(2002)
Blood
, vol.99
, Issue.1
, pp. 310-318
-
-
Kelly, L.M.1
Liu, Q.2
Kutok, J.L.3
Williams, I.R.4
Boulton, C.L.5
Gilliland, D.G.6
-
21
-
-
20444402664
-
FLT3-ITD and tyrosine kinase domain mutants induce 2 distinct phenotypes in a murine bone marrow transplantation model
-
DOI 10.1182/blood-2004-11-4430
-
Grundler R, Miething C, Thiede C, Peschel C, Duyster J. FLT3-ITD and tyrosine kinase domain mutants induce 2 distinct phenotypes in a murine bone marrow transplantation model. Blood. 2005; 105(12):4792-4799. (Pubitemid 40807305)
-
(2005)
Blood
, vol.105
, Issue.12
, pp. 4792-4799
-
-
Grundler, R.1
Miething, C.2
Thiede, C.3
Peschel, C.4
Duyster, J.5
-
22
-
-
35048848955
-
FLT3 mutations confer enhanced proliferation and survival properties to multipotent progenitors in a murine model of chronic myelomonocytic leukemia
-
Lee BH, Tothova Z, Levine RL, et al. FLT3 mutations confer enhanced proliferation and survival properties to multipotent progenitors in a murine model of chronic myelomonocytic leukemia. Cancer Cell. 2007;12(4):367-380.
-
(2007)
Cancer Cell
, vol.12
, Issue.4
, pp. 367-380
-
-
Lee, B.H.1
Tothova, Z.2
Levine, R.L.3
-
23
-
-
43549123118
-
Knock-in of an internal tandem duplication mutation into murine FLT3 confers myeloproliferative disease in a mouse model
-
Li L, Piloto O, Nguyen HB, et al. Knock-in of an internal tandem duplication mutation into murine FLT3 confers myeloproliferative disease in a mouse model. Blood. 2008;111(7):3849-3858.
-
(2008)
Blood
, vol.111
, Issue.7
, pp. 3849-3858
-
-
Li, L.1
Piloto, O.2
Nguyen, H.B.3
-
24
-
-
19944427369
-
Identification of a novel activating mutation (Y842C) within the activation loop of FLT3 in patients with acute myeloid leukemia (AML)
-
Kindler T, Breitenbuecher F, Kasper S, et al. Identification of a novel activating mutation (Y842C) within the activation loop of FLT3 in patients with acute myeloid leukemia (AML). Blood. 2005; 105(1):335-340.
-
(2005)
Blood
, vol.105
, Issue.1
, pp. 335-340
-
-
Kindler, T.1
Breitenbuecher, F.2
Kasper, S.3
-
25
-
-
36649000489
-
Identification of driver and passenger mutations of FLT3 by high-throughput DNA sequence analysis and functional assessment of candidate alleles
-
Frohling S, Scholl C, Levine RL, et al. Identification of driver and passenger mutations of FLT3 by high-throughput DNA sequence analysis and functional assessment of candidate alleles. Cancer Cell. 2007;12(6):501-513.
-
(2007)
Cancer Cell
, vol.12
, Issue.6
, pp. 501-513
-
-
Frohling, S.1
Scholl, C.2
Levine, R.L.3
-
26
-
-
0036839326
-
A new and recurrent activating length mutation in exon 20 of the FLT3 gene in acute myeloid leukemia
-
Spiekermann K, Bagrintseva K, Schoch C, Haferlach T, Hiddemann W, Schnittger S. A new and recurrent activating length mutation in exon 20 of the FLT3 gene in acute myeloid leukemia. Blood. 2002;100(9):3423-3425.
-
(2002)
Blood
, vol.100
, Issue.9
, pp. 3423-3425
-
-
Spiekermann, K.1
Bagrintseva, K.2
Schoch, C.3
Haferlach, T.4
Hiddemann, W.5
Schnittger, S.6
-
27
-
-
33645312560
-
Point mutations in the juxtamembrane domain of FLT3 define a new class of activating mutations in AML
-
Reindl C, Bagrintseva K, Vempati S, et al. Point mutations in the juxtamembrane domain of FLT3 define a new class of activating mutations in AML. Blood. 2006;107(9):3700-3707.
-
(2006)
Blood
, vol.107
, Issue.9
, pp. 3700-3707
-
-
Reindl, C.1
Bagrintseva, K.2
Vempati, S.3
-
28
-
-
0033758958
-
FLT3 internal tandem duplication mutations in adult acute myeloid leukaemia define a high-risk group
-
Abu-Duhier FM, Goodeve AC, Wilson GA, et al. FLT3 internal tandem duplication mutations in adult acute myeloid leukaemia define a high-risk group. Br J Haematol. 2000;111(1):190-195.
-
(2000)
Br J Haematol
, vol.111
, Issue.1
, pp. 190-195
-
-
Abu-Duhier, F.M.1
Goodeve, A.C.2
Wilson, G.A.3
-
29
-
-
0037097716
-
Analysis of FLT3-activating mutations in 979 patients with acute myelogenous leukemia: Association with FAB subtypes and identification of subgroups with poor prognosis
-
Thiede C, Steudel C, Mohr B, et al. Analysis of FLT3-activating mutations in 979 patients with acute myelogenous leukemia: association with FAB subtypes and identification of subgroups with poor prognosis. Blood. 2002;99(12):4326- 4335.
-
(2002)
Blood
, vol.99
, Issue.12
, pp. 4326-4335
-
-
Thiede, C.1
Steudel, C.2
Mohr, B.3
-
30
-
-
27744451026
-
No evidence that FLT3 status should be considered as an indicator for transplantation in acute myeloid leukemia (AML): An analysis of 1135 patients, excluding acute promyelocytic leukemia, from the UK MRC AML10 and 12 trials
-
Gale RE, Hills R, Kottaridis PD, et al. No evidence that FLT3 status should be considered as an indicator for transplantation in acute myeloid leukemia (AML): an analysis of 1135 patients, excluding acute promyelocytic leukemia, from the UK MRC AML10 and 12 trials. Blood. 2005; 106(10):3658-3665.
-
(2005)
Blood
, vol.106
, Issue.10
, pp. 3658-3665
-
-
Gale, R.E.1
Hills, R.2
Kottaridis, P.D.3
-
31
-
-
70350504884
-
Insertion of FLT3 internal tandem duplication in the tyrosine kinase domain-1 is associated with resistance to chemotherapy and inferior outcome
-
Kayser S, Schlenk RF, Londono MC, et al. Insertion of FLT3 internal tandem duplication in the tyrosine kinase domain-1 is associated with resistance to chemotherapy and inferior outcome. Blood. 2009;114(12):2386-2392.
-
(2009)
Blood
, vol.114
, Issue.12
, pp. 2386-2392
-
-
Kayser, S.1
Schlenk, R.F.2
Londono, M.C.3
-
32
-
-
33646431111
-
Size of FLT3 internal tandem duplication has prognostic significance in patients with acute myeloid leukemia
-
Stirewalt DL, Kopecky KJ, Meshinchi S, et al. Size of FLT3 internal tandem duplication has prognostic significance in patients with acute myeloid leukemia. Blood. 2006;107(9):3724-3726.
-
(2006)
Blood
, vol.107
, Issue.9
, pp. 3724-3726
-
-
Stirewalt, D.L.1
Kopecky, K.J.2
Meshinchi, S.3
-
33
-
-
33745628343
-
More on prognostic significance of FLT3/ITD size in acute myeloid leukemia (AML)
-
author reply 406
-
Kusec R, Jaksic O, Ostojic S, Kardum-Skelin I, Vrhovac R, Jaksic B. More on prognostic significance of FLT3/ITD size in acute myeloid leukemia (AML). Blood. 2006;108(1):405-406; author reply 406.
-
(2006)
Blood
, vol.108
, Issue.1
, pp. 405-406
-
-
Kusec, R.1
Jaksic, O.2
Ostojic, S.3
Kardum-Skelin, I.4
Vrhovac, R.5
Jaksic, B.6
-
34
-
-
33750369309
-
The size of duplication does not add to the prognostic significance of FLT3 internal tandem duplication in acute myeloid leukemia patients
-
Ponziani V, Gianfaldoni G, Mannelli F, et al. The size of duplication does not add to the prognostic significance of FLT3 internal tandem duplication in acute myeloid leukemia patients. Leukemia. 2006;20(11):2074-2076.
-
(2006)
Leukemia
, vol.20
, Issue.11
, pp. 2074-2076
-
-
Ponziani, V.1
Gianfaldoni, G.2
Mannelli, F.3
-
35
-
-
19944427850
-
Cytoplasmic nucleophosmin in acute myelogenous leukemia with a normal karyotype
-
DOI 10.1056/NEJMoa041974
-
Falini B, Mecucci C, Tiacci E, et al. Cytoplasmic nucleophosmin in acute myelogenous leukemia with a normal karyotype. N Engl J Med. 2005; 352(3):254-266. (Pubitemid 40110814)
-
(2005)
New England Journal of Medicine
, vol.352
, Issue.3
, pp. 254-266
-
-
Falini, B.1
Mecucci, C.2
Tiacci, E.3
Alcalay, M.4
Rosati, R.5
Pasqualucci, L.6
La Starza, R.7
Diverio, D.8
Colombo, E.9
Santucci, A.10
Bigerna, B.11
Pacini, R.12
Pucciarini, A.13
Liso, A.14
Vignetti, M.15
Fazi, P.16
Meani, N.17
Pettirossi, V.18
Saglio, G.19
Mandelli, F.20
Lo-Coco, F.21
Pelicci, P.-G.22
Martelli, M.F.23
more..
-
36
-
-
28444449081
-
Nucleophosmin gene mutations are predictors of favorable prognosis in acute myelogenous leukemia with a normal karyotype
-
Schnittger S, Schoch C, Kern W, et al. Nucleophosmin gene mutations are predictors of favorable prognosis in acute myelogenous leukemia with a normal karyotype. Blood. 2005;106(12): 3733-3739.
-
(2005)
Blood
, vol.106
, Issue.12
, pp. 3733-3739
-
-
Schnittger, S.1
Schoch, C.2
Kern, W.3
-
37
-
-
28444473100
-
Mutant nucleophosmin (NPM1) predicts favorable prognosis in younger adults with acute myeloid leukemia and normal cytogenetics: Interaction with other gene mutations
-
Dohner K, Schlenk RF, Habdank M, et al. Mutant nucleophosmin (NPM1) predicts favorable prognosis in younger adults with acute myeloid leukemia and normal cytogenetics: interaction with other gene mutations. Blood. 2005;106(12):3740-3746.
-
(2005)
Blood
, vol.106
, Issue.12
, pp. 3740-3746
-
-
Dohner, K.1
Schlenk, R.F.2
Habdank, M.3
-
38
-
-
28444446313
-
Mutations in nucleophosmin (NPM1) in acute myeloid leukemia (AML): Association with other gene abnormalities and previously established gene expression signatures and their favorable prognostic significance
-
Verhaak RG, Goudswaard CS, van Putten W, et al. Mutations in nucleophosmin (NPM1) in acute myeloid leukemia (AML): association with other gene abnormalities and previously established gene expression signatures and their favorable prognostic significance. Blood. 2005;106(12): 3747-3754.
-
(2005)
Blood
, vol.106
, Issue.12
, pp. 3747-3754
-
-
Verhaak, R.G.1
Goudswaard, C.S.2
Van Putten, W.3
-
39
-
-
33646557337
-
Prevalence and prognostic impact of NPM1 mutations in 1485 adult patients with acute myeloid leukemia (AML)
-
DOI 10.1182/blood-2005-08-3167
-
Thiede C, Koch S, Creutzig E, et al. Prevalence and prognostic impact of NPM1 mutations in 1485 adult patients with acute myeloid leukemia (AML). Blood. 2006;107(10):4011-4020. (Pubitemid 43726809)
-
(2006)
Blood
, vol.107
, Issue.10
, pp. 4011-4020
-
-
Thiede, C.1
Koch, S.2
Creutzig, E.3
Steudel, C.4
Illmer, T.5
Schaich, M.6
Ehninger, G.7
-
40
-
-
42949142189
-
Mutations and treatment outcome in cytogenetically normal acute myeloid leukemia
-
Schlenk RF, Dohner K, Krauter J, et al. Mutations and treatment outcome in cytogenetically normal acute myeloid leukemia. N Engl J Med. 2008; 358(18):1909-1918.
-
(2008)
N Engl J Med
, vol.358
, Issue.18
, pp. 1909-1918
-
-
Schlenk, R.F.1
Dohner, K.2
Krauter, J.3
-
41
-
-
41949090673
-
The impact of FLT3 internal tandem duplication mutant level, number, size, and interaction with NPM1 mutations in a large cohort of young adult patients with acute myeloid leukemia
-
Gale RE, Green C, Allen C, et al. The impact of FLT3 internal tandem duplication mutant level, number, size, and interaction with NPM1 mutations in a large cohort of young adult patients with acute myeloid leukemia. Blood. 2008;111(5): 2776-2784.
-
(2008)
Blood
, vol.111
, Issue.5
, pp. 2776-2784
-
-
Gale, R.E.1
Green, C.2
Allen, C.3
-
42
-
-
41949087055
-
Prognostic relevance of FLT3-TKD mutations in AML: The combination matters - An analysis of 3082 patients
-
Bacher U, Haferlach C, Kern W, Haferlach T, Schnittger S. Prognostic relevance of FLT3-TKD mutations in AML: the combination matters - an analysis of 3082 patients. Blood. 2008;111(5): 2527-2537.
-
(2008)
Blood
, vol.111
, Issue.5
, pp. 2527-2537
-
-
Bacher, U.1
Haferlach, C.2
Kern, W.3
Haferlach, T.4
Schnittger, S.5
-
43
-
-
23744444913
-
Prognostic significance of FLT3 internal tandem duplication and tyrosine kinase domain mutations for acute myeloid leukemia: A meta-analysis
-
Yanada M, Matsuo K, Suzuki T, Kiyoi H, Naoe T. Prognostic significance of FLT3 internal tandem duplication and tyrosine kinase domain mutations for acute myeloid leukemia: a meta-analysis. Leukemia. 2005;19(8):1345-1349.
-
(2005)
Leukemia
, vol.19
, Issue.8
, pp. 1345-1349
-
-
Yanada, M.1
Matsuo, K.2
Suzuki, T.3
Kiyoi, H.4
Naoe, T.5
-
44
-
-
12244282411
-
Incidence and prognostic value of FLT3 internal tandem duplication and D835 mutations in acute myeloid leukemia
-
Moreno I, Martin G, Bolufer P, et al. Incidence and prognostic value of FLT3 internal tandem duplication and D835 mutations in acute myeloid leukemia. Haematologica. 2003;88(1):19-24.
-
(2003)
Haematologica
, vol.88
, Issue.1
, pp. 19-24
-
-
Moreno, I.1
Martin, G.2
Bolufer, P.3
-
45
-
-
38949212204
-
FLT3 D835/I836 mutations are associated with poor disease-free survival and a distinct gene-expression signature among younger adults with de novo cytogenetically normal acute myeloid leukemia lacking FLT3 internal tandem duplications
-
Whitman SP, Ruppert AS, Radmacher MD, et al. FLT3 D835/I836 mutations are associated with poor disease-free survival and a distinct gene-expression signature among younger adults with de novo cytogenetically normal acute myeloid leukemia lacking FLT3 internal tandem duplications. Blood. 2008;111(3):1552- 1559.
-
(2008)
Blood
, vol.111
, Issue.3
, pp. 1552-1559
-
-
Whitman, S.P.1
Ruppert, A.S.2
Radmacher, M.D.3
-
46
-
-
34548029756
-
FLT3 tyrosine kinase domain mutations are biologically distinct from and have a significantly more favorable prognosis than FLT3 internal tandem duplications in patients with acute myeloid leukemia
-
Mead AJ, Linch DC, Hills RK, Wheatley K, Burnett AK, Gale RE. FLT3 tyrosine kinase domain mutations are biologically distinct from and have a significantly more favorable prognosis than FLT3 internal tandem duplications in patients with acute myeloid leukemia. Blood. 2007; 110(4):1262-1270.
-
(2007)
Blood
, vol.110
, Issue.4
, pp. 1262-1270
-
-
Mead, A.J.1
Linch, D.C.2
Hills, R.K.3
Wheatley, K.4
Burnett, A.K.5
Gale, R.E.6
-
47
-
-
0034936404
-
Identification of novel FLT-3 Asp835 mutations in adult acute myeloid leukaemia
-
Abu-Duhier FM, Goodeve AC, Wilson GA, Care RS, Peake IR, Reilly JT. Identification of novel FLT-3 Asp835 mutations in adult acute myeloid leukaemia. Br J Haematol. 2001;113(4):983-988.
-
(2001)
Br J Haematol
, vol.113
, Issue.4
, pp. 983-988
-
-
Abu-Duhier, F.M.1
Goodeve, A.C.2
Wilson, G.A.3
Care, R.S.4
Peake, I.R.5
Reilly, J.T.6
-
48
-
-
0035871889
-
Activating mutation of D835 within the activation loop of FLT3 in human hematologic malignancies
-
Yamamoto Y, Kiyoi H, Nakano Y, et al. Activating mutation of D835 within the activation loop of FLT3 in human hematologic malignancies. Blood. 2001;97(8):2434-2439.
-
(2001)
Blood
, vol.97
, Issue.8
, pp. 2434-2439
-
-
Yamamoto, Y.1
Kiyoi, H.2
Nakano, Y.3
-
49
-
-
19944427559
-
Patients with acute myeloid leukemia and an activating mutation in FLT3 respond to a small-molecule FLT3 tyrosine kinase inhibitor, PKC412
-
Stone RM, DeAngelo DJ, Klimek V, 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(1):54-60.
-
(2005)
Blood
, vol.105
, Issue.1
, pp. 54-60
-
-
Stone, R.M.1
DeAngelo, D.J.2
Klimek, V.3
-
50
-
-
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, et al. Plasma inhibitory activity (PIA): a pharmacodynamic assay reveals insights into the basis for cytotoxic response to FLT3 inhibitors. Blood. 2006;108(10): 3477-3483.
-
(2006)
Blood
, vol.108
, Issue.10
, pp. 3477-3483
-
-
Levis, M.1
Brown, P.2
Smith, B.D.3
-
51
-
-
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, et al. Single-agent CEP-701, a novel FLT3 inhibitor, shows biologic and clinical activity in patients with relapsed or refractory acute myeloid leukemia. Blood. 2004; 103(10):3669-3676. (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
-
52
-
-
33751173636
-
A phase 2 trial of the FLT3 inhibitor lestaurtinib (CEP701) as first-line treatment for older patients with acute myeloid leukemia not considered fit for intensive chemotherapy
-
Knapper S, Burnett AK, Littlewood T, et al. A phase 2 trial of the FLT3 inhibitor lestaurtinib (CEP701) as first-line treatment for older patients with acute myeloid leukemia not considered fit for intensive chemotherapy. Blood. 2006;108(10): 3262-3270.
-
(2006)
Blood
, vol.108
, Issue.10
, pp. 3262-3270
-
-
Knapper, S.1
Burnett, A.K.2
Littlewood, T.3
-
53
-
-
33751177110
-
The effects of lestaurtinib (CEP701) and PKC412 on primary AML blasts: The induction of cytotoxicity varies with dependence on FLT3 signaling in both FLT3-mutated and wild-type cases
-
Knapper S, Mills KI, Gilkes AF, Austin SJ, Walsh V, Burnett AK. The effects of lestaurtinib (CEP701) and PKC412 on primary AML blasts: the induction of cytotoxicity varies with dependence on FLT3 signaling in both FLT3-mutated and wild-type cases. Blood. 2006;108(10):3494-3503.
-
(2006)
Blood
, vol.108
, Issue.10
, pp. 3494-3503
-
-
Knapper, S.1
Mills, K.I.2
Gilkes, A.F.3
Austin, S.J.4
Walsh, V.5
Burnett, A.K.6
-
54
-
-
39149129114
-
Mutant FLT3: A direct target of sorafenib in acute myelogenous leukemia
-
Zhang W, Konopleva M, Shi YX, et al. Mutant FLT3: a direct target of sorafenib in acute myelogenous leukemia. J Natl Cancer Inst. 2008;100(3): 184-198.
-
(2008)
J Natl Cancer Inst
, vol.100
, Issue.3
, pp. 184-198
-
-
Zhang, W.1
Konopleva, M.2
Shi, Y.X.3
-
55
-
-
69249221392
-
Compassionate use of sorafenib in FLT3-ITD-positive acute myeloid leukemia: Sustained regression before and after allogeneic stem cell transplantation
-
Metzelder S, Wang Y, Wollmer E, et al. Compassionate use of sorafenib in FLT3-ITD-positive acute myeloid leukemia: sustained regression before and after allogeneic stem cell transplantation. Blood. 2009;113(26):6567-6571.
-
(2009)
Blood
, vol.113
, Issue.26
, pp. 6567-6571
-
-
Metzelder, S.1
Wang, Y.2
Wollmer, E.3
-
56
-
-
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(7):1425-1432.
-
(2010)
Blood
, vol.115
, Issue.7
, pp. 1425-1432
-
-
Pratz, K.W.1
Sato, T.2
Murphy, K.M.3
Stine, A.4
Rajkhowa, T.5
Levis, M.6
-
57
-
-
0043245991
-
SU5416, a small molecule tyrosine kinase receptor inhibitor, has biologic activity in patients with refractory acute myeloid leukemia or myelodysplastic syndromes
-
Giles FJ, Stopeck AT, Silverman LR, et al. SU5416, a small molecule tyrosine kinase receptor inhibitor, has biologic activity in patients with refractory acute myeloid leukemia or myelodysplastic syndromes. Blood. 2003;102(3):795-801.
-
(2003)
Blood
, vol.102
, Issue.3
, pp. 795-801
-
-
Giles, F.J.1
Stopeck, A.T.2
Silverman, L.R.3
-
58
-
-
2442584575
-
Effects of SU5416, a small molecule tyrosine kinase receptor inhibitor, on FLT3 expression and phosphorylation in patients with refractory acute myeloid leukemia
-
O'Farrell AM, Yuen HA, Smolich B, et al. Effects of SU5416, a small molecule tyrosine kinase receptor inhibitor, on FLT3 expression and phosphorylation in patients with refractory acute myeloid leukemia. Leuk Res. 2004;28(7):679-689.
-
(2004)
Leuk Res
, vol.28
, Issue.7
, pp. 679-689
-
-
O'Farrell, A.M.1
Yuen, H.A.2
Smolich, B.3
-
59
-
-
0141993064
-
A phase 2 clinical study of SU5416 in patients with refractory acute myeloid leukemia
-
Fiedler W, Mesters R, Tinnefeld H, et al. A phase 2 clinical study of SU5416 in patients with refractory acute myeloid leukemia. Blood. 2003;102(8): 2763-2767.
-
(2003)
Blood
, vol.102
, Issue.8
, pp. 2763-2767
-
-
Fiedler, W.1
Mesters, R.2
Tinnefeld, H.3
-
60
-
-
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, 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(15):5465-5476.
-
(2003)
Clin Cancer Res
, vol.9
, Issue.15
, pp. 5465-5476
-
-
O'Farrell, A.M.1
Foran, J.M.2
Fiedler, W.3
-
61
-
-
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
-
Fiedler W, Serve H, Dohner H, 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(3):986-993.
-
(2005)
Blood
, vol.105
, Issue.3
, pp. 986-993
-
-
Fiedler, W.1
Serve, H.2
Dohner, H.3
-
62
-
-
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
-
DeAngelo DJ, Stone RM, Heaney ML, 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 pharmacodynamics. Blood. 2006;108(12):3674-3681.
-
(2006)
Blood
, vol.108
, Issue.12
, pp. 3674-3681
-
-
DeAngelo, D.J.1
Stone, R.M.2
Heaney, M.L.3
-
63
-
-
24144487571
-
Phase II evaluation of the tyrosine kinase inhibitor MLN518 in patients with acute myeloid leukemia (AML) bearing a FLT3 internal tandem duplication (ITD) mutation
-
Abstract 1792
-
DeAngelo DJ, Stone RM, Heaney ML, et al. Phase II evaluation of the tyrosine kinase inhibitor MLN518 in patients with acute myeloid leukemia (AML) bearing a FLT3 internal tandem duplication (ITD) mutation. Blood). 2004;104:496. Abstract 1792.
-
(2004)
Blood
, vol.104
, pp. 496
-
-
DeAngelo, D.J.1
Stone, R.M.2
Heaney, M.L.3
-
64
-
-
67349137674
-
A phase I dose escalation study of KW-2449, an oral multi-kinase inhibitor against FLT3, Abl, FGFR1 and aurora in patients with relapsed/ refractory AML, ALL and MDS or resistant/intolerant CML
-
Abstract 2967
-
Cortes J, Robos GJ, Kantarjian HM, et al. A phase I dose escalation study of KW-2449, an oral multi-kinase inhibitor against FLT3, Abl, FGFR1 and aurora in patients with relapsed/ refractory AML, ALL and MDS or resistant/intolerant CML. Blood. 2008;112. Abstract 2967.
-
(2008)
Blood
, pp. 112
-
-
Cortes, J.1
Robos, G.J.2
Kantarjian, H.M.3
-
65
-
-
62949087552
-
A pharmacodynamic study of the FLT3 inhibitor KW-2449 yields insight into the basis for clinical response
-
Pratz KW, Cortes J, Roboz GJ, et al. A pharmacodynamic study of the FLT3 inhibitor KW-2449 yields insight into the basis for clinical response. Blood. 2009;113(17):3938-3946.
-
(2009)
Blood
, vol.113
, Issue.17
, pp. 3938-3946
-
-
Pratz, K.W.1
Cortes, J.2
Roboz, G.J.3
-
66
-
-
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, et al. AC220 is a uniquely potent and selective inhibitor of FLT3 for the treatment of acute myeloid leukemia (AML). Blood. 2009;114(14):2984-2992.
-
(2009)
Blood
, vol.114
, Issue.14
, pp. 2984-2992
-
-
Zarrinkar, P.P.1
Gunawardane, R.N.2
Cramer, M.D.3
-
67
-
-
77950421846
-
AC220, a potent, selective second generation FLT3 receptor tyrosine kinase (RTK) inhibitor, in a first-in-human (FIH) phase 1 AML study
-
Abstract 636
-
Cortes J, Foran J, Ghirdaladze D, et al. AC220, a potent, selective second generation FLT3 receptor tyrosine kinase (RTK) inhibitor, in a first-in-human (FIH) phase 1 AML study. Blood. 2009; 114. Abstract 636.
-
(2009)
Blood
, pp. 114
-
-
Cortes, J.1
Foran, J.2
Ghirdaladze, D.3
-
68
-
-
69249212433
-
The FLT3 inhibitor tandutinib (formerly MLN518) has sequence-independent synergistic effects with cytarabine and daunorubicin
-
Schittenhelm MM, Kampa KM, Yee KW, Heinrich MC. The FLT3 inhibitor tandutinib (formerly MLN518) has sequence-independent synergistic effects with cytarabine and daunorubicin. Cell Cycle. 2009;8(16):2621-2630.
-
(2009)
Cell Cycle
, vol.8
, Issue.16
, pp. 2621-2630
-
-
Schittenhelm, M.M.1
Kampa, K.M.2
Yee, K.W.3
Heinrich, M.C.4
-
69
-
-
45749129047
-
The FLT3 inhibitor PKC412 in combination with cytostatic drugs in vitro in acute myeloid leukemia
-
DOI 10.1007/s00280-007-0623-4
-
Mollgard L, Deneberg S, Nahi H, et al. The FLT3 inhibitor PKC412 in combination with cytostatic drugs in vitro in acute myeloid leukemia. Cancer Chemother Pharmacol. 2008;62(3):439-448. (Pubitemid 351871802)
-
(2008)
Cancer Chemotherapy and Pharmacology
, vol.62
, Issue.3
, pp. 439-448
-
-
Mollgard, L.1
Deneberg, S.2
Nahi, H.3
Bengtzen, S.4
Jonsson-Videsater, K.5
Fioretos, T.6
Andersson, A.7
Paul, C.8
Lehmann, S.9
-
70
-
-
3843142735
-
In vitro studies of a FLT3 inhibitor combined with chemotherapy: Sequence of administration is important to achieve synergistic cytotoxic effects
-
Levis M, Pham R, Smith BD, Small D. In vitro studies of a FLT3 inhibitor combined with chemotherapy: sequence of administration is important to achieve synergistic cytotoxic effects. Blood. 2004;104(4):1145-1150.
-
(2004)
Blood
, vol.104
, Issue.4
, pp. 1145-1150
-
-
Levis, M.1
Pham, R.2
Smith, B.D.3
Small, D.4
-
71
-
-
10244277976
-
Synergistic effect of SU11248 with cytarabine or daunorubicin on FLT3 ITD-positive leukemic cells
-
Yee KW, Schittenhelm M, O'Farrell AM, et al. Synergistic effect of SU11248 with cytarabine or daunorubicin on FLT3 ITD-positive leukemic cells. Blood. 2004;104(13):4202-4209.
-
(2004)
Blood
, vol.104
, Issue.13
, pp. 4202-4209
-
-
Yee, K.W.1
Schittenhelm, M.2
O'Farrell, A.M.3
-
72
-
-
38849174002
-
Phase 1/2 study of tandutinib (MLN518) plus standard induction chemotherapy in newly diagnosed acute myeloid leukemia
-
Abstract 158
-
DeAngelo DJ, Amrein PC, Kovacsovics TJ, et al. Phase 1/2 study of tandutinib (MLN518) plus standard induction chemotherapy in newly diagnosed acute myeloid leukemia. Blood. 2006;108. Abstract 158.
-
(2006)
Blood
, pp. 108
-
-
DeAngelo, D.J.1
Amrein, P.C.2
Kovacsovics, T.J.3
-
73
-
-
77950423964
-
A Phase 1b study of midostaurin (PKC412) in combination with daunorubicin and cytarabine induction and high-dose cytarabine consolidation in patients under age 61 with newly diagnosed de novo acute myeloid leukemia: Overall survival of patients whose blasts have FLT3 mutations is similar to those with wild-type FLT3
-
Abstract 634
-
Stone RM, Fischer T, Paquette R, et al. A Phase 1b study of midostaurin (PKC412) in combination with daunorubicin and cytarabine induction and high-dose cytarabine consolidation in patients under age 61 with newly diagnosed de novo acute myeloid leukemia: Overall survival of patients whose blasts have FLT3 mutations is similar to those with wild-type FLT3. Blood. 2009;114. Abstract 634.
-
(2009)
Blood
, pp. 114
-
-
Stone, R.M.1
Fischer, T.2
Paquette, R.3
-
74
-
-
77951645227
-
Phase I/II study of combination therapy with sorafenib, idarubicin, and cytarabine in younger patients with acute myeloid leukemia
-
Ravandi F, Cortes JE, Jones D, et al. Phase I/II study of combination therapy with sorafenib, idarubicin, and cytarabine in younger patients with acute myeloid leukemia. J Clin Oncol. 2010; 28(11):1856-1862.
-
(2010)
J Clin Oncol
, vol.28
, Issue.11
, pp. 1856-1862
-
-
Ravandi, F.1
Cortes, J.E.2
Jones, D.3
-
75
-
-
77954474254
-
Results from a randomized trial of salvage chemotherapy followed by lestaurtinib for FLT3 mutant AML patients in first relapse
-
Abstract 788
-
Levis M, Ravandi F, Wang ES, et al. Results from a randomized trial of salvage chemotherapy followed by lestaurtinib for FLT3 mutant AML patients in first relapse. Blood. 2009;114. Abstract 788.
-
(2009)
Blood
, pp. 114
-
-
Levis, M.1
Ravandi, F.2
Wang, E.S.3
-
76
-
-
3843117641
-
Suppression of leukemia expressing wild-type or ITD-mutant FLT3 receptor by a fully human anti-FLT3 neutralizing antibody
-
Li Y, Li H, Wang MN, et al. Suppression of leukemia expressing wild-type or ITD-mutant FLT3 receptor by a fully human anti-FLT3 neutralizing antibody. Blood. 2004;104(4):1137-1144.
-
(2004)
Blood
, vol.104
, Issue.4
, pp. 1137-1144
-
-
Li, Y.1
Li, H.2
Wang, M.N.3
-
77
-
-
14044249427
-
Inhibitory anti- FLT3 antibodies are capable of mediating anti-body- dependent cell-mediated cytotoxicity and reducing engraftment of acute myelogenous leukemia blasts in nonobese diabetic/severe combined immunodeficient mice
-
Piloto O, Levis M, Huso D, et al. Inhibitory anti- FLT3 antibodies are capable of mediating anti-body- dependent cell-mediated cytotoxicity and reducing engraftment of acute myelogenous leukemia blasts in nonobese diabetic/severe combined immunodeficient mice. Cancer Res. 2005; 65(4):1514-1522.
-
(2005)
Cancer Res
, vol.65
, Issue.4
, pp. 1514-1522
-
-
Piloto, O.1
Levis, M.2
Huso, D.3
-
78
-
-
33646432479
-
IMC-EB10, an anti-FLT3 monoclonal antibody, prolongs survival and reduces nonobese diabetic/severe combined immunodeficient engraftment of some acute lymphoblastic leukemia cell lines and primary leukemic samples
-
Piloto O, Nguyen B, Huso D, et al. IMC-EB10, an anti-FLT3 monoclonal antibody, prolongs survival and reduces nonobese diabetic/severe combined immunodeficient engraftment of some acute lymphoblastic leukemia cell lines and primary leukemic samples. Cancer Res. 2006;66(9):4843-4851.
-
(2006)
Cancer Res
, vol.66
, Issue.9
, pp. 4843-4851
-
-
Piloto, O.1
Nguyen, B.2
Huso, D.3
-
79
-
-
33846936758
-
Prolonged exposure to FLT3 inhibitors leads to resistance via activation of parallel signaling pathways
-
Piloto O, Wright M, Brown P, Kim KT, Levis M, Small D. Prolonged exposure to FLT3 inhibitors leads to resistance via activation of parallel signaling pathways. Blood. 2007;109(4):1643-1652.
-
(2007)
Blood
, vol.109
, Issue.4
, pp. 1643-1652
-
-
Piloto, O.1
Wright, M.2
Brown, P.3
Kim, K.T.4
Levis, M.5
Small, D.6
-
80
-
-
65449158845
-
A novel molecular mechanism of primary resistance to FLT3-kinase inhibitors in AML
-
Breitenbuecher F, Markova B, Kasper S, et al. A novel molecular mechanism of primary resistance to FLT3-kinase inhibitors in AML. Blood. 2009; 113(17):4063-4073.
-
(2009)
Blood
, vol.113
, Issue.17
, pp. 4063-4073
-
-
Breitenbuecher, F.1
Markova, B.2
Kasper, S.3
-
81
-
-
7244251613
-
Variable sensitivity of FLT3 activation loop mutations to the small molecule tyrosine kinase inhibitor MLN518
-
DOI 10.1182/blood-2003-12-4446
-
Clark JJ, Cools J, Curley DP, et al. Variable sensitivity of FLT3 activation loop mutations to the small molecule tyrosine kinase inhibitor MLN518. Blood. 2004;104(9):2867-2872. (Pubitemid 39434973)
-
(2004)
Blood
, vol.104
, Issue.9
, pp. 2867-2872
-
-
Clark, J.J.1
Cools, J.2
Curley, D.P.3
Yu, J.-C.4
Lokker, N.A.5
Giese, N.A.6
Gilliland, D.G.7
-
82
-
-
1542313903
-
Mutations in the tyrosine kinase domain of FLT3 define a new molecular mechanism of acquired drug resistance to PTK inhibitors in FLT3-ITD-transformed hematopoietic cells
-
Bagrintseva K, Schwab R, Kohl TM, et al. Mutations in the tyrosine kinase domain of FLT3 define a new molecular mechanism of acquired drug resistance to PTK inhibitors in FLT3-ITD-transformed hematopoietic cells. Blood. 2004; 103(6):2266-2275.
-
(2004)
Blood
, vol.103
, Issue.6
, pp. 2266-2275
-
-
Bagrintseva, K.1
Schwab, R.2
Kohl, T.M.3
-
83
-
-
0038156174
-
Sensitivity toward tyrosine kinase inhibitors varies between different activating mutations of the FLT3 receptor
-
Grundler R, Thiede C, Miething C, Steudel C, Peschel C, Duyster J. Sensitivity toward tyrosine kinase inhibitors varies between different activating mutations of the FLT3 receptor. Blood. 2003; 102(2):646-651.
-
(2003)
Blood
, vol.102
, Issue.2
, pp. 646-651
-
-
Grundler, R.1
Thiede, C.2
Miething, C.3
Steudel, C.4
Peschel, C.5
Duyster, J.6
-
84
-
-
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(5682):399-401.
-
(2004)
Science
, vol.305
, Issue.5682
, pp. 399-401
-
-
Shah, N.P.1
Tran, C.2
Lee, F.Y.3
Chen, P.4
Norris, D.5
Sawyers, C.L.6
-
85
-
-
4644240387
-
Prediction of resistance to small molecule FLT3 inhibitors: Implications for molecularly targeted therapy of acute leukemia
-
DOI 10.1158/0008-5472.CAN-04-2148
-
Cools J, Mentens N, Furet P, et al. Prediction of resistance to small molecule FLT3 inhibitors: implications for molecularly targeted therapy of acute leukemia. Cancer Res. 2004;64(18):6385-6389. (Pubitemid 39297890)
-
(2004)
Cancer Research
, vol.64
, Issue.18
, pp. 6385-6389
-
-
Cools, J.1
Mentens, N.2
Furet, P.3
Fabbro, D.4
Clark, J.J.5
Griffin, J.D.6
Marynen, P.7
Gilliland, D.G.8
-
86
-
-
30144432781
-
Clinical resistance to the kinase inhibitor PKC412 in acute myeloid leukemia by mutation of Asn-676 in the FLT3 tyrosine kinase domain
-
Heidel F, Solem FK, Breitenbuecher F, et al. Clinical resistance to the kinase inhibitor PKC412 in acute myeloid leukemia by mutation of Asn-676 in the FLT3 tyrosine kinase domain. Blood. 2006; 107(1):293-300.
-
(2006)
Blood
, vol.107
, Issue.1
, pp. 293-300
-
-
Heidel, F.1
Solem, F.K.2
Breitenbuecher, F.3
-
87
-
-
66149152278
-
FMS-like tyrosine kinase 3-internal tandem duplication tyrosine kinase inhibitors display a nonoverlapping profile of resistance mutations in vitro
-
von Bubnoff N, Engh RA, Aberg E, Sanger J, Peschel C, Duyster J. FMS-like tyrosine kinase 3-internal tandem duplication tyrosine kinase inhibitors display a nonoverlapping profile of resistance mutations in vitro. Cancer Res. 2009;69(7): 3032-3041.
-
(2009)
Cancer Res
, vol.69
, Issue.7
, pp. 3032-3041
-
-
Von Bubnoff, N.1
Engh, R.A.2
Aberg, E.3
Sanger, J.4
Peschel, C.5
Duyster, J.6
-
88
-
-
65449117656
-
Enhanced activation of STAT pathways and overexpression of survivin confer resistance to FLT3 inhibitors and could be therapeutic targets in AML
-
Zhou J, Bi C, Janakakumara JV, et al. Enhanced activation of STAT pathways and overexpression of survivin confer resistance to FLT3 inhibitors and could be therapeutic targets in AML. Blood. 2009;113(17):4052-4062.
-
(2009)
Blood
, vol.113
, Issue.17
, pp. 4052-4062
-
-
Zhou, J.1
Bi, C.2
Janakakumara, J.V.3
-
89
-
-
0036595143
-
Inhibition of mutant FLT3 receptors in leukemia cells by the small molecule tyrosine kinase inhibitor PKC412
-
Weisberg E, Boulton C, Kelly LM, et al. Inhibition of mutant FLT3 receptors in leukemia cells by the small molecule tyrosine kinase inhibitor PKC412. Cancer Cell. 2002;1(5):433-443.
-
(2002)
Cancer Cell
, vol.1
, Issue.5
, pp. 433-443
-
-
Weisberg, E.1
Boulton, C.2
Kelly, L.M.3
-
90
-
-
77953070292
-
Mechanisms of resistance against PKC412 in resistant FLT3-ITD positive human acute myeloid leukemia cells
-
Stolzel F, Steudel C, Oelschlagel U, et al. Mechanisms of resistance against PKC412 in resistant FLT3-ITD positive human acute myeloid leukemia cells. Ann Hematol. 2010;89(7):653-662.
-
(2010)
Ann Hematol
, vol.89
, Issue.7
, pp. 653-662
-
-
Stolzel, F.1
Steudel, C.2
Oelschlagel, U.3
-
91
-
-
77950452556
-
Increased plasma FLT3 ligand levels following chemotherapy may interfere with the clinical efficacy of FLT3 inhibitors
-
Abstract 937
-
Sato TKS, Burnett AK, White P, Levis M. Increased plasma FLT3 ligand levels following chemotherapy may interfere with the clinical efficacy of FLT3 inhibitors. Blood. 2009;114. Abstract 937.
-
(2009)
Blood
, pp. 114
-
-
Sato, T.K.S.1
Burnett, A.K.2
White, P.3
Levis, M.4
-
92
-
-
73949096431
-
FLT3-ITD up-regulates MCL-1 to promote survival of stem cells in acute myeloid leukemia via FLT3-ITD-specific STAT5 activation
-
Yoshimoto G, Miyamoto T, Jabbarzadeh-Tabrizi S, et al. FLT3-ITD up-regulates MCL-1 to promote survival of stem cells in acute myeloid leukemia via FLT3-ITD-specific STAT5 activation. Blood. 2009;114(24):5034-5043.
-
(2009)
Blood
, vol.114
, Issue.24
, pp. 5034-5043
-
-
Yoshimoto, G.1
Miyamoto, T.2
Jabbarzadeh-Tabrizi, S.3
-
93
-
-
34447642522
-
BH3 mimetic ABT-737 neutralizes resistance to FLT3 inhibitor treatment mediated by FLT3-independent expression of BCL2 in primary AML blasts
-
Kohl TM, Hellinger C, Ahmed F, et al. BH3 mimetic ABT-737 neutralizes resistance to FLT3 inhibitor treatment mediated by FLT3-independent expression of BCL2 in primary AML blasts. Leukemia. 2007;21(8):1763-1772.
-
(2007)
Leukemia
, vol.21
, Issue.8
, pp. 1763-1772
-
-
Kohl, T.M.1
Hellinger, C.2
Ahmed, F.3
-
94
-
-
10744230464
-
Biologic and clinical significance of the FLT3 transcript level in acute myeloid leukemia
-
Ozeki K, Kiyoi H, Hirose Y, et al. Biologic and clinical significance of the FLT3 transcript level in acute myeloid leukemia. Blood. 2004;103(5): 1901-1908.
-
(2004)
Blood
, vol.103
, Issue.5
, pp. 1901-1908
-
-
Ozeki, K.1
Kiyoi, H.2
Hirose, Y.3
-
95
-
-
33749337234
-
Simultaneous activation of multiple signal transduction pathways confers poor prognosis in acute myelogenous leukemia
-
DOI 10.1182/blood-2006-02-003475
-
Kornblau SM, Womble M, Qiu YH, et al. Simultaneous activation of multiple signal transduction pathways confers poor prognosis in acute myelogenous leukemia. Blood. 2006;108(7):2358-2365. (Pubitemid 44497520)
-
(2006)
Blood
, vol.108
, Issue.7
, pp. 2358-2365
-
-
Kornblau, S.M.1
Womble, M.2
Yi, H.Q.3
Jackson, C.E.4
Chen, W.5
Konopleva, M.6
Estey, E.H.7
Andreeff, M.8
-
96
-
-
1542327671
-
Combination of rapamycin and protein tyrosine kinase (PTK) inhibitors for the treatment of leukemias caused by oncogenic PTKs
-
Mohi MG, Boulton C, Gu TL, et al. Combination of rapamycin and protein tyrosine kinase (PTK) inhibitors for the treatment of leukemias caused by oncogenic PTKs. Proc Natl Acad Sci U S A. 2004; 101(9):3130-3135.
-
(2004)
Proc Natl Acad Sci U S A
, vol.101
, Issue.9
, pp. 3130-3135
-
-
Mohi, M.G.1
Boulton, C.2
Gu, T.L.3
-
97
-
-
43549112362
-
Potentiation of antileukemic therapies by the dual PI3K/ PDK-1 inhibitor, BAG956: Effects on BCR-ABL-and mutant FLT3-expressing cells
-
Weisberg E, Banerji L, Wright RD, et al. Potentiation of antileukemic therapies by the dual PI3K/ PDK-1 inhibitor, BAG956: effects on BCR-ABL-and mutant FLT3-expressing cells. Blood. 2008; 111(7):3723-3734.
-
(2008)
Blood
, vol.111
, Issue.7
, pp. 3723-3734
-
-
Weisberg, E.1
Banerji, L.2
Wright, R.D.3
-
98
-
-
33750483896
-
The anti-tumor effects of sunitinib (formerly SU11248) against a variety of human hematologic malignancies: Enhancement of growth inhibition via inhibition of mammalian target of rapamycin signaling
-
Ikezoe T, Nishioka C, Tasaka T, et al. The anti-tumor effects of sunitinib (formerly SU11248) against a variety of human hematologic malignancies: enhancement of growth inhibition via inhibition of mammalian target of rapamycin signaling. Mol Cancer Ther. 2006;5(10):2522-2530.
-
(2006)
Mol Cancer Ther
, vol.5
, Issue.10
, pp. 2522-2530
-
-
Ikezoe, T.1
Nishioka, C.2
Tasaka, T.3
-
99
-
-
40749143500
-
Blockade of MEK/ERK signaling enhances sunitinib-induced growth inhibition and apoptosis of leukemia cells possessing activating mutations of the FLT3 gene
-
Nishioka C, Ikezoe T, Yang J, et al. Blockade of MEK/ERK signaling enhances sunitinib-induced growth inhibition and apoptosis of leukemia cells possessing activating mutations of the FLT3 gene. Leuk Res. 2008;32(6):865-872.
-
(2008)
Leuk Res
, vol.32
, Issue.6
, pp. 865-872
-
-
Nishioka, C.1
Ikezoe, T.2
Yang, J.3
-
100
-
-
42249109027
-
Heat shock protein 90 inhibition is cytotoxic to primary AML cells expressing mutant FLT3 and results in altered downstream signalling
-
Al Shaer L, Walsby E, Gilkes A, et al. Heat shock protein 90 inhibition is cytotoxic to primary AML cells expressing mutant FLT3 and results in altered downstream signalling. Br J Haematol. 2008;141(4):483-493.
-
(2008)
Br J Haematol
, vol.141
, Issue.4
, pp. 483-493
-
-
Al Shaer, L.1
Walsby, E.2
Gilkes, A.3
-
101
-
-
43049173740
-
MS-275, a novel histone deacetylase inhibitor with selectivity against HDAC1, induces degradation of FLT3 via inhibition of chaperone function of heat shock protein 90 in AML cells
-
Nishioka C, Ikezoe T, Yang J, Takeuchi S, Koeffler HP, Yokoyama A. MS-275, a novel histone deacetylase inhibitor with selectivity against HDAC1, induces degradation of FLT3 via inhibition of chaperone function of heat shock protein 90 in AML cells. Leuk Res. 2008;32(9):1382-1392.
-
(2008)
Leuk Res
, vol.32
, Issue.9
, pp. 1382-1392
-
-
Nishioka, C.1
Ikezoe, T.2
Yang, J.3
Takeuchi, S.4
Koeffler, H.P.5
Yokoyama, A.6
-
103
-
-
0030789242
-
Human acute myeloid leukemia is organized as a hierarchy that originates from a primitive hematopoietic cell
-
Bonnet D, Dick JE. Human acute myeloid leukemia is organized as a hierarchy that originates from a primitive hematopoietic cell. Nat Med. 1997;3(7):730-737.
-
(1997)
Nat Med
, vol.3
, Issue.7
, pp. 730-737
-
-
Bonnet, D.1
Dick, J.E.2
-
104
-
-
11144235821
-
Enforced expression of an Flt3 internal tandem duplication in human CD34+ cells confers properties of self-renewal and enhanced erythropoiesis
-
Chung KY, Morrone G, Schuringa JJ, Wong B, Dorn DC, Moore MA. Enforced expression of an Flt3 internal tandem duplication in human CD34+ cells confers properties of self-renewal and enhanced erythropoiesis. Blood. 2005;105(1):77-84.
-
(2005)
Blood
, vol.105
, Issue.1
, pp. 77-84
-
-
Chung, K.Y.1
Morrone, G.2
Schuringa, J.J.3
Wong, B.4
Dorn, D.C.5
Moore, M.A.6
-
105
-
-
33947220301
-
FLT3/ITD expression increases expansion, survival and entry into cell cycle of human haematopoietic stem/progenitor cells
-
Li L, Piloto O, Kim KT, et al. FLT3/ITD expression increases expansion, survival and entry into cell cycle of human haematopoietic stem/progenitor cells. Br J Haematol. 2007;137(1):64-75.
-
(2007)
Br J Haematol
, vol.137
, Issue.1
, pp. 64-75
-
-
Li, L.1
Piloto, O.2
Kim, K.T.3
-
106
-
-
0036785393
-
Studies of FLT3 mutations in paired presentation and relapse samples from patients with acute myeloid leukemia: Implications for the role of FLT3 mutations in leukemogenesis, minimal residual disease detection, and possible therapy with FLT3 inhibitors
-
Kottaridis PD, Gale RE, Langabeer SE, Frew ME, Bowen DT, Linch DC. Studies of FLT3 mutations in paired presentation and relapse samples from patients with acute myeloid leukemia: implications for the role of FLT3 mutations in leukemogenesis, minimal residual disease detection, and possible therapy with FLT3 inhibitors. Blood. 2002;100(7):2393-2398.
-
(2002)
Blood
, vol.100
, Issue.7
, pp. 2393-2398
-
-
Kottaridis, P.D.1
Gale, R.E.2
Langabeer, S.E.3
Frew, M.E.4
Bowen, D.T.5
Linch, D.C.6
-
107
-
-
1642301466
-
Heterogeneous patterns of FLT3 Asp(835) mutations in relapsed de novo acute myeloid leukemia: A comparative analysis of 120 paired diagnostic and relapse bone marrow samples
-
Shih LY, Huang CF, Wu JH, et al. Heterogeneous patterns of FLT3 Asp(835) mutations in relapsed de novo acute myeloid leukemia: a comparative analysis of 120 paired diagnostic and relapse bone marrow samples. Clin Cancer Res. 2004; 10(4):1326-1332.
-
(2004)
Clin Cancer Res
, vol.10
, Issue.4
, pp. 1326-1332
-
-
Shih, L.Y.1
Huang, C.F.2
Wu, J.H.3
-
108
-
-
46949098927
-
A rapid, one step assay for simultaneous detection of FLT3/ITD and NPM1 mutations in AML with normal cytogenetics
-
Huang Q, Chen W, Gaal KK, Slovak ML, Stein A, Weiss LM. A rapid, one step assay for simultaneous detection of FLT3/ITD and NPM1 mutations in AML with normal cytogenetics. Br J Haematol. 2008;142(3):489-492.
-
(2008)
Br J Haematol
, vol.142
, Issue.3
, pp. 489-492
-
-
Huang, Q.1
Chen, W.2
Gaal, K.K.3
Slovak, M.L.4
Stein, A.5
Weiss, L.M.6
-
109
-
-
0033043084
-
Molecular evolution of acute myeloid leukaemia in relapse: Unstable N- Ras and FLT3 genes compared with p53 gene
-
Nakano Y, Kiyoi H, Miyawaki S, et al. Molecular evolution of acute myeloid leukaemia in relapse: unstable N-ras and FLT3 genes compared with p53 gene. Br J Haematol. 1999;104(4):659-664. (Pubitemid 29143481)
-
(1999)
British Journal of Haematology
, vol.104
, Issue.4
, pp. 659-664
-
-
Nakano, Y.1
Kiyoi, H.2
Miyawaki, S.3
Asou, N.4
Ohno, R.5
Saito, H.6
Naoe, T.7
-
110
-
-
37449023112
-
Monitoring of minimal residual disease in acute myeloid leukemia
-
Kern W, Haferlach C, Haferlach T, Schnittger S. Monitoring of minimal residual disease in acute myeloid leukemia. Cancer. 2008;112(1):4-16.
-
(2008)
Cancer
, vol.112
, Issue.1
, pp. 4-16
-
-
Kern, W.1
Haferlach, C.2
Haferlach, T.3
Schnittger, S.4
-
111
-
-
22144469473
-
Internal tandem duplications of the FLT3 gene are present in leukemia stem cells
-
Levis M, Murphy KM, Pham R, et al. Internal tandem duplications of the FLT3 gene are present in leukemia stem cells. Blood. 2005;106(2):673-680.
-
(2005)
Blood
, vol.106
, Issue.2
, pp. 673-680
-
-
Levis, M.1
Murphy, K.M.2
Pham, R.3
-
112
-
-
0036738149
-
Stromal cells prevent apoptosis of AML cells by up-regulation of anti-apoptotic proteins
-
Konopleva M, Konoplev S, Hu W, Zaritskey AY, Afanasiev BV, Andreeff M. Stromal cells prevent apoptosis of AML cells by up-regulation of anti-apoptotic proteins. Leukemia. 2002;16(9):1713-1724.
-
(2002)
Leukemia
, vol.16
, Issue.9
, pp. 1713-1724
-
-
Konopleva, M.1
Konoplev, S.2
Hu, W.3
Zaritskey, A.Y.4
Afanasiev, B.V.5
Andreeff, M.6
-
113
-
-
47549089642
-
Resistance to FLT3 inhibition in an in vitro model of primary AML cells with a stem cell phenotype in a defined microenvironment
-
Mony U, Jawad M, Seedhouse C, Russell N, Pallis M. Resistance to FLT3 inhibition in an in vitro model of primary AML cells with a stem cell phenotype in a defined microenvironment. Leukemia. 2008;22(7):1395-1401.
-
(2008)
Leukemia
, vol.22
, Issue.7
, pp. 1395-1401
-
-
Mony, U.1
Jawad, M.2
Seedhouse, C.3
Russell, N.4
Pallis, M.5
-
114
-
-
0141461414
-
Interaction between leukemic-cell VLA-4 and stromal fibronectin is a decisive factor for minimal residual disease of acute myelogenous leukemia
-
Matsunaga T, Takemoto N, Sato T, et al. Interaction between leukemic-cell VLA-4 and stromal fibronectin is a decisive factor for minimal residual disease of acute myelogenous leukemia. Nat Med. 2003;9(9):1158-1165.
-
(2003)
Nat Med
, vol.9
, Issue.9
, pp. 1158-1165
-
-
Matsunaga, T.1
Takemoto, N.2
Sato, T.3
-
115
-
-
39149106436
-
Combination therapy of an anticancer drug with the FNIII14 peptide of fibronectin effectively over-comes cell adhesion-mediated drug resistance of acute myelogenous leukemia
-
Matsunaga T, Fukai F, Miura S, et al. Combination therapy of an anticancer drug with the FNIII14 peptide of fibronectin effectively over-comes cell adhesion-mediated drug resistance of acute myelogenous leukemia. Leukemia. 2008; 22(2):353-360.
-
(2008)
Leukemia
, vol.22
, Issue.2
, pp. 353-360
-
-
Matsunaga, T.1
Fukai, F.2
Miura, S.3
-
116
-
-
13744255245
-
CXCR4 regulates migration and development of human acute myelogenous leukemia stem cells in transplanted NOD/SCID mice
-
Tavor S, Petit I, Porozov S, et al. CXCR4 regulates migration and development of human acute myelogenous leukemia stem cells in transplanted NOD/SCID mice. Cancer Res. 2004;64(8):2817-2824.
-
(2004)
Cancer Res
, vol.64
, Issue.8
, pp. 2817-2824
-
-
Tavor, S.1
Petit, I.2
Porozov, S.3
-
117
-
-
17044418635
-
Flt3 ligand and the Flt3 receptor regulate hematopoietic cell migration by modulating the SDF-1alpha(CXCL12)/ CXCR4 axis
-
Fukuda S, Broxmeyer HE, Pelus LM. Flt3 ligand and the Flt3 receptor regulate hematopoietic cell migration by modulating the SDF-1alpha(CXCL12)/ CXCR4 axis. Blood. 2005;105(8):3117-3126.
-
(2005)
Blood
, vol.105
, Issue.8
, pp. 3117-3126
-
-
Fukuda, S.1
Broxmeyer, H.E.2
Pelus, L.M.3
-
118
-
-
3142620882
-
Relation between CXCR-4 expression, Flt3 mutations, and unfavorable prognosis of adult acute myeloid leukemia
-
Rombouts EJ, Pavic B, Lowenberg B, Ploemacher RE. Relation between CXCR-4 expression, Flt3 mutations, and unfavorable prognosis of adult acute myeloid leukemia. Blood. 2004;104(2):550-557.
-
(2004)
Blood
, vol.104
, Issue.2
, pp. 550-557
-
-
Rombouts, E.J.1
Pavic, B.2
Lowenberg, B.3
Ploemacher, R.E.4
-
119
-
-
69549086437
-
Dissection of PIM serine/threonine kinases in FLT3-ITDinduced leukemogenesis reveals PIM1 as regulator of CXCL12-CXCR4-mediated homing and migration
-
Grundler R, Brault L, Gasser C, et al. Dissection of PIM serine/threonine kinases in FLT3-ITDinduced leukemogenesis reveals PIM1 as regulator of CXCL12-CXCR4-mediated homing and migration. J Exp Med. 2009;206(9):1957-1970.
-
(2009)
J Exp Med
, vol.206
, Issue.9
, pp. 1957-1970
-
-
Grundler, R.1
Brault, L.2
Gasser, C.3
-
120
-
-
67650410440
-
Chemosensitization of acute myeloid leukemia (AML) following mobilization by the CXCR4 antagonist AMD3100
-
Nervi B, Ramirez P, Rettig MP, et al. Chemosensitization of acute myeloid leukemia (AML) following mobilization by the CXCR4 antagonist AMD3100. Blood. 2009;113(24):6206-6214.
-
(2009)
Blood
, vol.113
, Issue.24
, pp. 6206-6214
-
-
Nervi, B.1
Ramirez, P.2
Rettig, M.P.3
-
121
-
-
34249692617
-
CXCR4 antagonists mobilize childhood acute lymphoblastic leukemia cells into the peripheral blood and inhibit engraftment
-
Juarez J, Dela Pena A, Baraz R, et al. CXCR4 antagonists mobilize childhood acute lymphoblastic leukemia cells into the peripheral blood and inhibit engraftment. Leukemia. 2007;21(6): 1249-1257.
-
(2007)
Leukemia
, vol.21
, Issue.6
, pp. 1249-1257
-
-
Juarez, J.1
Dela Pena, A.2
Baraz, R.3
-
122
-
-
67650367598
-
Targeting the leukemia microenvironment by CXCR4 inhibition overcomes resistance to kinase inhibitors and chemotherapy in AML
-
Zeng Z, Shi YX, Samudio IJ, et al. Targeting the leukemia microenvironment by CXCR4 inhibition overcomes resistance to kinase inhibitors and chemotherapy in AML. Blood. 2009;113(24): 6215-6224.
-
(2009)
Blood
, vol.113
, Issue.24
, pp. 6215-6224
-
-
Zeng, Z.1
Shi, Y.X.2
Samudio, I.J.3
-
123
-
-
0036624916
-
AFLT3-targeted tyrosine kinase inhibitor is cytotoxic to leukemia cells in vitro and in vivo
-
Levis M, Allebach J, Tse KF, et al. AFLT3-targeted tyrosine kinase inhibitor is cytotoxic to leukemia cells in vitro and in vivo. Blood. 2002;99(11): 3885-3891.
-
(2002)
Blood
, vol.99
, Issue.11
, pp. 3885-3891
-
-
Levis, M.1
Allebach, J.2
Tse, K.F.3
-
124
-
-
33847195060
-
Antitumor activity of sorafenib in FLT3-driven leukemic cells
-
Auclair D, Miller D, Yatsula V, et al. Antitumor activity of sorafenib in FLT3-driven leukemic cells. Leukemia. 2007;21(3):439-445.
-
(2007)
Leukemia
, vol.21
, Issue.3
, pp. 439-445
-
-
Auclair, D.1
Miller, D.2
Yatsula, V.3
-
125
-
-
33846930383
-
The ability of sorafenib to inhibit oncogenic PDGFRbeta and FLT3 mutants and overcome resistance to other small molecule inhibitors
-
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(1):27-34.
-
(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
-
126
-
-
0037108298
-
SU5416 and SU5614 inhibit kinase activity of wild-type and mutant FLT3 receptor tyrosine kinase
-
Yee KW, O'Farrell AM, Smolich BD, et al. SU5416 and SU5614 inhibit kinase activity of wild-type and mutant FLT3 receptor tyrosine kinase. Blood. 2002;100(8):2941-2949.
-
(2002)
Blood
, vol.100
, Issue.8
, pp. 2941-2949
-
-
Yee, K.W.1
O'Farrell, A.M.2
Smolich, B.D.3
-
127
-
-
0037441745
-
The protein tyrosine kinase inhibitor SU5614 inhibits FLT3 and induces growth arrest and apoptosis in AML-derived cell lines expressing a constitutively activated FLT3
-
Spiekermann K, Dirschinger RJ, Schwab R, et al. The protein tyrosine kinase inhibitor SU5614 inhibits FLT3 and induces growth arrest and apoptosis in AML-derived cell lines expressing a constitutively activated FLT3. Blood. 2003;101(4): 1494-1504.
-
(2003)
Blood
, vol.101
, Issue.4
, pp. 1494-1504
-
-
Spiekermann, K.1
Dirschinger, R.J.2
Schwab, R.3
-
128
-
-
12244301581
-
In vivo antitumor activity of SU11248, a novel tyrosine kinase inhibitor targeting vascular endothelial growth factor and platelet-derived growth factor receptors: Determination of a pharmacokinetic/pharmacodynamic relationship
-
Mendel DB, Laird AD, Xin X, et al. In vivo antitumor activity of SU11248, a novel tyrosine kinase inhibitor targeting vascular endothelial growth factor and platelet-derived growth factor receptors: determination of a pharmacokinetic/pharmacodynamic relationship. Clin Cancer Res. 2003; 9(1):327-337.
-
(2003)
Clin Cancer Res
, vol.9
, Issue.1
, pp. 327-337
-
-
Mendel, D.B.1
Laird, A.D.2
Xin, X.3
-
129
-
-
0038204144
-
SU11248 is a novel FLT3 tyrosine kinase inhibitor with potent activity in vitro and in vivo
-
O'Farrell AM, Abrams TJ, Yuen HA, et al. SU11248 is a novel FLT3 tyrosine kinase inhibitor with potent activity in vitro and in vivo. Blood. 2003;101(9): 3597-3605.
-
(2003)
Blood
, vol.101
, Issue.9
, pp. 3597-3605
-
-
O'Farrell, A.M.1
Abrams, T.J.2
Yuen, H.A.3
-
130
-
-
0034888832
-
Efficacy of the novel selective platelet-derived growth factor receptor antagonist CT52923 on cellular proliferation, migration, and suppression of neointima following vascular injury
-
Yu JC, Lokker NA, Hollenbach S, et al. Efficacy of the novel selective platelet-derived growth factor receptor antagonist CT52923 on cellular proliferation, migration, and suppression of neointima following vascular injury. J Pharmacol Exp Ther. 2001;298(3):1172-1178.
-
(2001)
J Pharmacol Exp Ther
, vol.298
, Issue.3
, pp. 1172-1178
-
-
Yu, J.C.1
Lokker, N.A.2
Hollenbach, S.3
-
131
-
-
0013102301
-
CT53518, a novel selective FLT3 antagonist for the treatment of acute myelogenous leukemia (AML)
-
Kelly LM, Yu JC, Boulton CL, et al. CT53518, a novel selective FLT3 antagonist for the treatment of acute myelogenous leukemia (AML). Cancer Cell. 2002;1(5):421-432.
-
(2002)
Cancer Cell
, vol.1
, Issue.5
, pp. 421-432
-
-
Kelly, L.M.1
Yu, J.C.2
Boulton, C.L.3
-
132
-
-
7244253001
-
Effects of MLN518, a dual FLT3 and KIT inhibitor, on normal and malignant hematopoiesis
-
Griswold IJ, Shen LJ, La Rosee P, et al. Effects of MLN518, a dual FLT3 and KIT inhibitor, on normal and malignant hematopoiesis. Blood. 2004;104(9): 2912-2918.
-
(2004)
Blood
, vol.104
, Issue.9
, pp. 2912-2918
-
-
Griswold, I.J.1
Shen, L.J.2
La Rosee, P.3
-
133
-
-
70349566478
-
KW-2449, a novel multikinase inhibitor, suppresses the growth of leukemia cells with FLT3 mutations or T315I-mutated BCR/ABL translocation
-
Shiotsu Y, Kiyoi H, Ishikawa Y, et al. KW-2449, a novel multikinase inhibitor, suppresses the growth of leukemia cells with FLT3 mutations or T315I-mutated BCR/ABL translocation. Blood. 2009;114(8):1607-1617.
-
(2009)
Blood
, vol.114
, Issue.8
, pp. 1607-1617
-
-
Shiotsu, Y.1
Kiyoi, H.2
Ishikawa, Y.3
-
134
-
-
67349142616
-
FLT3 inhibition and mechanisms of drug resistance in mutant FLT3-positive AML
-
Weisberg E, Barrett R, Liu Q, Stone R, Gray N, Griffin JD. FLT3 inhibition and mechanisms of drug resistance in mutant FLT3-positive AML. Drug Resist Updat. 2009;12(3):81-89.
-
(2009)
Drug Resist Updat
, vol.12
, Issue.3
, pp. 81-89
-
-
Weisberg, E.1
Barrett, R.2
Liu, Q.3
Stone, R.4
Gray, N.5
Griffin, J.D.6
|