-
1
-
-
78649905124
-
Independent prognostic variables in acute myeloid leukaemia
-
Smith ML, Hills RK, Grimwade D. Independent prognostic variables in acute myeloid leukaemia. Blood Rev 2010; 25: 39-51.
-
(2010)
Blood Rev
, vol.25
, pp. 39-51
-
-
Smith, M.L.1
Hills, R.K.2
Grimwade, D.3
-
2
-
-
67650351086
-
Structural and functional alterations of FLT3 in acute myeloid leukemia
-
Meshinchi S, Appelbaum FR. Structural and functional alterations of FLT3 in acute myeloid leukemia. Clin Cancer Res 2009; 15: 4263-4269.
-
(2009)
Clin Cancer Res
, vol.15
, pp. 4263-4269
-
-
Meshinchi, S.1
Appelbaum, F.R.2
-
3
-
-
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: 7233-7239.
-
(2001)
Cancer Res
, vol.61
, pp. 7233-7239
-
-
Whitman, S.P.1
Archer, K.J.2
Feng, L.3
Baldus, C.4
Becknell, B.5
Carlson, B.D.6
-
4
-
-
33845254595
-
Clinical implications of FLT3 mutations in pediatric AML
-
Meshinchi S, Alonzo TA, Stirewalt DL, Zwaan M, Zimmerman M, Reinhardt D et al. Clinical implications of FLT3 mutations in pediatric AML. Blood 2006; 108: 3654-3661.
-
(2006)
Blood
, vol.108
, pp. 3654-3661
-
-
Meshinchi, S.1
Alonzo, T.A.2
Stirewalt, D.L.3
Zwaan, M.4
Zimmerman, M.5
Reinhardt, D.6
-
5
-
-
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: 1262-1270.
-
(2007)
Blood
, vol.110
, 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
-
6
-
-
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, Mrozek K, Paschka P, Langer C 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: 1552-1559.
-
(2008)
Blood
, vol.111
, pp. 1552-1559
-
-
Whitman, S.P.1
Ruppert, A.S.2
Radmacher, M.D.3
Mrozek, K.4
Paschka, P.5
Langer, C.6
-
7
-
-
80052713073
-
The clinical development of FLT3 inhibitors in acute myeloid leukemia
-
Knapper S. The clinical development of FLT3 inhibitors in acute myeloid leukemia. Expert Opin Investig Drugs 2011; 20: 1377-1395.
-
(2011)
Expert Opin Investig Drugs
, vol.20
, pp. 1377-1395
-
-
Knapper, S.1
-
8
-
-
78649931161
-
Will newer tyrosine kinase inhibitors have an impact in AML?
-
Levis MJ. Will newer tyrosine kinase inhibitors have an impact in AML? Best Pract Res Clin Haematol 2010; 23: 489-494.
-
(2010)
Best Pract Res Clin Haematol
, vol.23
, pp. 489-494
-
-
Levis, M.J.1
-
9
-
-
84863784729
-
Validation of FLT3-ITD as a therapeutic target in human acute myeloid leukemia
-
(abstract 937)
-
Smith CC, Chin J, Wang Q, Salerno S, Damon LE, Hunt JP et al. Validation of FLT3-ITD as a therapeutic target in human acute myeloid leukemia. Blood (ASH Annual Meeting Abstracts) 2011; 118 (abstract 937).
-
(2011)
Blood (ASH Annual Meeting Abstracts)
, vol.118
-
-
Smith, C.C.1
Chin, J.2
Wang, Q.3
Salerno, S.4
Damon, L.E.5
Hunt, J.P.6
-
11
-
-
77950949478
-
Aurora kinase inhibitors: Novel small molecules with promising activity in acute myeloid and Philadelphiapositive leukemias
-
Moore AS, Blagg J, Linardopoulos S, Pearson AD. Aurora kinase inhibitors: novel small molecules with promising activity in acute myeloid and Philadelphiapositive leukemias. Leukemia 2010; 24: 671-678.
-
(2010)
Leukemia
, vol.24
, pp. 671-678
-
-
Moore, A.S.1
Blagg, J.2
Linardopoulos, S.3
Pearson, A.D.4
-
12
-
-
33749409412
-
Validating Aurora B as an anti-cancer drug target
-
Girdler F, Gascoigne KE, Eyers PA, Hartmuth S, Crafter C, Foote KM et al. Validating Aurora B as an anti-cancer drug target. J Cell Sci 2006; 119: 3664-3675.
-
(2006)
J Cell Sci
, vol.119
, pp. 3664-3675
-
-
Girdler, F.1
Gascoigne, K.E.2
Eyers, P.A.3
Hartmuth, S.4
Crafter, C.5
Foote, K.M.6
-
13
-
-
39049166077
-
Aurora kinase inhibitors: Identification and preclinical validation of their biomarkers
-
Carpinelli P, Moll J. Aurora kinase inhibitors: identification and preclinical validation of their biomarkers. Expert Opin Ther Targets 2008; 12: 69-80.
-
(2008)
Expert Opin Ther Targets
, vol.12
, pp. 69-80
-
-
Carpinelli, P.1
Moll, J.2
-
14
-
-
33745275629
-
The chromosomal passenger complex: Guiding Aurora-B through mitosis
-
Vader G, Medema RH, Lens SM. The chromosomal passenger complex: guiding Aurora-B through mitosis. J Cell Biol 2006; 173: 833-837.
-
(2006)
J Cell Biol
, vol.173
, pp. 833-837
-
-
Vader, G.1
Medema, R.H.2
Lens, S.M.3
-
15
-
-
82955217793
-
Phase I/II study to assess the safety, efficacy, and pharmacokinetics of barasertib (AZD1152) in patients with advanced acute myeloid leukemia
-
Lowenberg B, Muus P, Ossenkoppele G, Rousselot P, Cahn JY, Ifrah N et al. Phase I/II study to assess the safety, efficacy, and pharmacokinetics of barasertib (AZD1152) in patients with advanced acute myeloid leukemia. Blood 2011; 118: 6030-6036.
-
(2011)
Blood
, vol.118
, pp. 6030-6036
-
-
Lowenberg, B.1
Muus, P.2
Ossenkoppele, G.3
Rousselot, P.4
Cahn, J.Y.5
Ifrah, N.6
-
16
-
-
81155124082
-
Phase 2 study of MLN8237 an investigational Aurora A kinase (AAK) inhibitor in patients with acute myelogenous leukemia (AML) or myelodysplastic syndromes (MDS)
-
(abstract 3273)
-
Goldberg SL, Fenaux P, Craig MD, Gyan E, Lister J, Kassis J et al. Phase 2 study of MLN8237, an investigational Aurora A kinase (AAK) inhibitor in patients with acute myelogenous leukemia (AML) or myelodysplastic syndromes (MDS). Blood (ASH Annual Meeting Abstracts) 2010; 116 (abstract 3273).
-
(2010)
Blood (ASH Annual Meeting Abstracts)
, pp. 116
-
-
Goldberg, S.L.1
Fenaux, P.2
Craig, M.D.3
Gyan, E.4
Lister, J.5
Kassis, J.6
-
17
-
-
77954715614
-
Imidazopyridine derivatives as inhibitors of Aurora kinases: Lead optimization studies toward the identification of an orally bioavailable preclinical development candidate
-
Bavetsias V, Large JM, Sun C, Bouloc N, Kosmopoulou M, Matteucci M et al. Imidazopyridine derivatives as inhibitors of Aurora kinases: lead optimization studies toward the identification of an orally bioavailable preclinical development candidate. J Med Chem 2010; 53: 5213-5228.
-
(2010)
J Med Chem
, vol.53
, pp. 5213-5228
-
-
Bavetsias, V.1
Large, J.M.2
Sun, C.3
Bouloc, N.4
Kosmopoulou, M.5
Matteucci, M.6
-
18
-
-
35649014837
-
Hit generation and exploration: Imidazopyridine derivatives as inhibitors of Aurora kinases
-
Bavetsias V, Sun C, Bouloc N, Reynisson J, Workman P, Linardopoulos S et al. Hit generation and exploration: imidazopyridine derivatives as inhibitors of Aurora kinases. Bioorg Med Chem Lett 2007; 17: 6567-6571.
-
(2007)
Bioorg Med Chem Lett
, vol.17
, pp. 6567-6571
-
-
Bavetsias, V.1
Sun, C.2
Bouloc, N.3
Reynisson, J.4
Workman, P.5
Linardopoulos, S.6
-
19
-
-
37549027270
-
Mechanism of action of the Aurora kinase inhibitor CCT129202 and in vivo quantification of biological activity
-
Chan F, Sun C, Perumal M, Nguyen QD, Bavetsias V, McDonald E et al. Mechanism of action of the Aurora kinase inhibitor CCT129202 and in vivo quantification of biological activity. Mol Cancer Ther 2007; 6: 3147-3157.
-
(2007)
Mol Cancer Ther
, vol.6
, pp. 3147-3157
-
-
Chan, F.1
Sun, C.2
Perumal, M.3
Nguyen, Q.D.4
Bavetsias, V.5
McDonald, E.6
-
21
-
-
0038365363
-
Detection of FLT3 internal tandem duplication and D835 mutations by a multiplex polymerase chain reaction and capillary electrophoresis assay
-
Murphy KM, Levis M, Hafez MJ, Geiger T, Cooper LC, Smith BD et al. Detection of FLT3 internal tandem duplication and D835 mutations by a multiplex polymerase chain reaction and capillary electrophoresis assay. J Mol Diagn 2003; 5: 96-102.
-
(2003)
J Mol Diagn
, vol.5
, pp. 96-102
-
-
Murphy, K.M.1
Levis, M.2
Hafez, M.J.3
Geiger, T.4
Cooper, L.C.5
Smith, B.D.6
-
22
-
-
77952812169
-
Guidelines for the welfare and use of animals in cancer research
-
Workman P, Aboagye EO, Balkwill F, Balmain A, Bruder G, Chaplin DJ et al. Guidelines for the welfare and use of animals in cancer research. Br J Cancer 2010; 102: 1555-1577.
-
(2010)
Br J Cancer
, vol.102
, pp. 1555-1577
-
-
Workman, P.1
Aboagye, E.O.2
Balkwill, F.3
Balmain, A.4
Bruder, G.5
Chaplin, D.J.6
-
23
-
-
84863775225
-
Saturation mutagenesis of FLT3-ITD: AC220-resistance-conferring kinase domain mutations are restricted to a limited number of residues and are cross-resistant to sorafenib in vitro
-
(abstract 4737)
-
Smith CC, Damon L, Salerno S, Shah NP. Saturation mutagenesis of FLT3-ITD: AC220-resistance-conferring kinase domain mutations are restricted to a limited number of residues and are cross-resistant to sorafenib in vitro. Am Assoc Cancer Res (AACR) Meeting Abstracts 2011 (abstract 4737).
-
(2011)
Am Assoc Cancer Res (AACR) Meeting Abstracts
-
-
Smith, C.C.1
Damon, L.2
Salerno, S.3
Shah, N.P.4
-
25
-
-
0027461633
-
Close physical linkage of the FLT1 and FLT3 genes on chromosome 13 in man and chromosome 5 in mouse
-
Rosnet O, Stephenson D, Mattei MG, Marchetto S, Shibuya M, Chapman VM et al. Close physical linkage of the FLT1 and FLT3 genes on chromosome 13 in man and chromosome 5 in mouse. Oncogene 1993; 8: 173-179.
-
(1993)
Oncogene
, vol.8
, pp. 173-179
-
-
Rosnet, O.1
Stephenson, D.2
Mattei, M.G.3
Marchetto, S.4
Shibuya, M.5
Chapman, V.M.6
-
26
-
-
34547673146
-
A novel FLT3 inhibitor FI-700 selectively suppresses the growth of leukemia cells with FLT3 mutations
-
Kiyoi H, Shiotsu Y, Ozeki K, Yamaji S, Kosugi H, Umehara H et al. A novel FLT3 inhibitor FI-700 selectively suppresses the growth of leukemia cells with FLT3 mutations. Clin Cancer Res 2007; 13: 4575-4582.
-
(2007)
Clin Cancer Res
, vol.13
, pp. 4575-4582
-
-
Kiyoi, H.1
Shiotsu, Y.2
Ozeki, K.3
Yamaji, S.4
Kosugi, H.5
Umehara, H.6
-
27
-
-
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, Müller 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: 3907-3914.
-
(2000)
Blood
, vol.96
, pp. 3907-3914
-
-
Mizuki, M.1
Fenski, R.2
Halfter, H.3
Matsumura, I.4
Schmidt, R.5
Müller, C.6
-
28
-
-
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: 2984-2992.
-
(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
-
29
-
-
7244251613
-
Variable sensitivity of FLT3 activation loop mutations to the small molecule tyrosine kinase inhibitor MLN518
-
Clark JJ, Cools J, Curley DP, Yu JC, Lokker NA, Giese NA et al. Variable sensitivity of FLT3 activation loop mutations to the small molecule tyrosine kinase inhibitor MLN518. Blood 2004; 104: 2867-2872.
-
(2004)
Blood
, vol.104
, 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
-
30
-
-
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: 3032-3041.
-
(2009)
Cancer Res
, vol.69
, pp. 3032-3041
-
-
Von Bubnoff, N.1
Engh, R.A.2
Aberg, E.3
Sanger, J.4
Peschel, C.5
Duyster, J.6
-
31
-
-
84863780489
-
Analysis of in vitro activity of the clinically-active ABL/FLT3 inhibitor Ponatinib (AP24534) against AC220-resistant FLT3-ITD mutants
-
(abstract 930)
-
Smith CC, Damon LE, Zhu X, Salerno S, Shah N. Analysis of in vitro activity of the clinically-active ABL/FLT3 inhibitor Ponatinib (AP24534) against AC220-resistant FLT3-ITD mutants. Blood (ASH Annual Meeting Abstracts) 2011; 118 (abstract 930).
-
(2011)
Blood (ASH Annual Meeting Abstracts)
, vol.118
-
-
Smith, C.C.1
Damon, L.E.2
Zhu, X.3
Salerno, S.4
Shah, N.5
-
32
-
-
84904282055
-
PLX3397 is an investigational selective FLT3 inhibitor that retains activity against the clinicallyrelevant FLT3-ITD/F691 L 'gatekeeper' mutation in vitro
-
(abstract 764)
-
Smith CC, Perl AE, Lasater E, Zhang C, Jeschke GR, Damon LE et al. PLX3397 is an investigational selective FLT3 inhibitor that retains activity against the clinicallyrelevant FLT3-ITD/F691 L 'gatekeeper' mutation in vitro. Blood (ASH Annual Meeting Abstracts) 2011; 118 (abstract 764).
-
(2011)
Blood (ASH Annual Meeting Abstracts)
, pp. 118
-
-
Smith, C.C.1
Perl, A.E.2
Lasater, E.3
Zhang, C.4
Jeschke, G.R.5
Damon, L.E.6
-
33
-
-
84886725614
-
Activity of allosteric, switch-pocket, ABL/FLT3 kinase inhibitor DCC2036 against cultured and primary aml progenitors with FLT-ITD or FLT3 kinase domain mutations
-
(abstract 2611)
-
Fiskus W, Smith CC, Smith J, Wise SC, Lasater E, Damon LE et al. Activity of allosteric, switch-pocket, ABL/FLT3 kinase inhibitor DCC2036 against cultured and primary aml progenitors with FLT-ITD or FLT3 kinase domain mutations. Blood (ASH Annual Meeting Abstracts) 2011; 118 (abstract 2611).
-
(2011)
Blood (ASH Annual Meeting Abstracts)
, pp. 118
-
-
Fiskus, W.1
Smith, C.C.2
Smith, J.3
Wise, S.C.4
Lasater, E.5
Damon, L.E.6
-
34
-
-
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, Lipka DB, Kasper S, Thiede MH 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: 293-300.
-
(2006)
Blood
, vol.107
, pp. 293-300
-
-
Heidel, F.1
Solem, F.K.2
Breitenbuecher, F.3
Lipka, D.B.4
Kasper, S.5
Thiede, M.H.6
-
35
-
-
0036786289
-
Internal tandem duplication of FLT3 in relapsed acute myeloid leukemia: A comparative analysis of bone marrow samples from 108 adult patients at diagnosis and relapse
-
Shih LY, Huang CF, Wu JH, Lin TL, Dunn P, Wang PN et al. Internal tandem duplication of FLT3 in relapsed acute myeloid leukemia: a comparative analysis of bone marrow samples from 108 adult patients at diagnosis and relapse. Blood 2002; 100: 2387-2392.
-
(2002)
Blood
, vol.100
, pp. 2387-2392
-
-
Shih, L.Y.1
Huang, C.F.2
Wu, J.H.3
Lin, T.L.4
Dunn, P.5
Wang, P.N.6
-
36
-
-
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: 1425-1432.
-
(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
-
37
-
-
50949113696
-
Segmental uniparental disomy is a commonly acquired genetic event in relapsed acute myeloid leukemia
-
Raghavan M, Smith LL, Lillington DM, Chaplin T, Kakkas I, Molloy G et al. Segmental uniparental disomy is a commonly acquired genetic event in relapsed acute myeloid leukemia. Blood 2008; 112: 814-821.
-
(2008)
Blood
, vol.112
, pp. 814-821
-
-
Raghavan, M.1
Smith, L.L.2
Lillington, D.M.3
Chaplin, T.4
Kakkas, I.5
Molloy, G.6
-
38
-
-
80855133514
-
Loss of the wild-type allele contributes to myeloid expansion and disease aggressiveness in FLT3/ITD knockin mice
-
Li L, Bailey E, Greenblatt S, Huso D, Small D. Loss of the wild-type allele contributes to myeloid expansion and disease aggressiveness in FLT3/ITD knockin mice. Blood 2011; 118: 4935-4945.
-
(2011)
Blood
, vol.118
, pp. 4935-4945
-
-
Li, L.1
Bailey, E.2
Greenblatt, S.3
Huso, D.4
Small, D.5
-
39
-
-
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, Schaich M, Schakel U, Platzbecker U 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: 4326-4335.
-
(2002)
Blood
, vol.99
, pp. 4326-4335
-
-
Thiede, C.1
Steudel, C.2
Mohr, B.3
Schaich, M.4
Schakel, U.5
Platzbecker, U.6
-
40
-
-
27244453278
-
Acute myeloid leukaemia with FLT3 gene mutations of both internal tandem duplication and point mutation type
-
Chen W, Jones D, Medeiros LJ, Luthra R, Lin P. Acute myeloid leukaemia with FLT3 gene mutations of both internal tandem duplication and point mutation type. Br J Haematol 2005; 130: 726-728.
-
(2005)
Br J Haematol
, vol.130
, pp. 726-728
-
-
Chen, W.1
Jones, D.2
Medeiros, L.J.3
Luthra, R.4
Lin, P.5
-
41
-
-
0242551845
-
FLT3 mutations are associated with other molecular lesions in AML
-
Carnicer MJ, Nomdedeu JF, Lasa A, Estivill C, Brunet S, Aventin A et al. FLT3 mutations are associated with other molecular lesions in AML. Leuk Res 2004; 28: 19-23.
-
(2004)
Leuk Res
, vol.28
, pp. 19-23
-
-
Carnicer, M.J.1
Nomdedeu, J.F.2
Lasa, A.3
Estivill, C.4
Brunet, S.5
Aventin, A.6
|