-
1
-
-
3242734038
-
Receptor tyrosine kinase signaling and trafficking-paradigms revisited
-
Barbieri, M. A., Ramkumar, T. P., Fernadez-Pol, S., Chen, P. I. and Stahl, P. D. (2004) Receptor tyrosine kinase signaling and trafficking-paradigms revisited. Curr. Top. Microbiol. Immunol. 286, 1-20
-
(2004)
Curr. Top. Microbiol. Immunol.
, vol.286
, pp. 1-20
-
-
Barbieri, M.A.1
Ramkumar, T.P.2
Fernadez-Pol, S.3
Chen, P.I.4
Stahl, P.D.5
-
2
-
-
1942445085
-
Endocytosis: Signaling from endocytic membranes to the nucleus
-
Benmerah, A. (2004) Endocytosis: signaling from endocytic membranes to the nucleus. Curr. Biol. 14, R314-R316
-
(2004)
Curr. Biol.
, vol.14
-
-
Benmerah, A.1
-
3
-
-
0242443214
-
Integrative nuclear FGFR1 signaling (INFS) as a part of a universal 'feed-forward-and-gate' signaling module that controls cell growth and differentiation
-
Stachowiak, M. K., Fang, X., Myers, J. M. et al. (2003) Integrative nuclear FGFR1 signaling (INFS) as a part of a universal 'feed-forward-and-gate' signaling module that controls cell growth and differentiation. J. Cell Biochem. 90, 662-691
-
(2003)
J. Cell Biochem.
, vol.90
, pp. 662-691
-
-
Stachowiak, M.K.1
Fang, X.2
Myers, J.M.3
-
4
-
-
3242804413
-
Biology of chronic myelogenous leukemia: Signaling pathways of initiation and transformation
-
Melo, J. V. and Deininger, M. W. (2004) Biology of chronic myelogenous leukemia: signaling pathways of initiation and transformation. Hematol. Oncol. Clin. North Am. 18, 545-568
-
(2004)
Hematol. Oncol. Clin. North Am.
, vol.18
, pp. 545-568
-
-
Melo, J.V.1
Deininger, M.W.2
-
5
-
-
1242307380
-
JAK/STAT, Raf/MEK/ERK, PI3K/Akt and BCR-ABL in cell cycle progression and leukemogenesis
-
Steelman, L. S., Pohnert, S. C., Shelton, J. G., Franklin, R. A., Bertrand, F. E. and McCubrey, J. A. (2004) JAK/STAT, Raf/MEK/ERK, PI3K/Akt and BCR-ABL in cell cycle progression and leukemogenesis. Leukemia 18, 189-218
-
(2004)
Leukemia
, vol.18
, pp. 189-218
-
-
Steelman, L.S.1
Pohnert, S.C.2
Shelton, J.G.3
Franklin, R.A.4
Bertrand, F.E.5
McCubrey, J.A.6
-
8
-
-
0022967572
-
Phenotypic change from transformed to normal induced by benzoquinonoid ansamycins accompanies inactivation of p60src in rat kidney cells infected with Rous sarcoma virus
-
Uehara, Y., Hori, M., Takeuchi, T. and Umezawa, H. (1986) Phenotypic change from transformed to normal induced by benzoquinonoid ansamycins accompanies inactivation of p60src in rat kidney cells infected with Rous sarcoma virus. Mol. Cell. Biol. 6, 2198-2206
-
(1986)
Mol. Cell. Biol.
, vol.6
, pp. 2198-2206
-
-
Uehara, Y.1
Hori, M.2
Takeuchi, T.3
Umezawa, H.4
-
9
-
-
0021932292
-
Screening of agents which convert 'transformed morphology' of Rous sarcoma virus-infected rat kidney cells to 'normal morphology': Identification of an active agent as herbimycin and its inhibition of intracellular src kinase
-
Uehara, Y., Hori, M., Takeuchi, T. and Umezawa, H. (1985) Screening of agents which convert 'transformed morphology' of Rous sarcoma virus-infected rat kidney cells to 'normal morphology': identification of an active agent as herbimycin and its inhibition of intracellular src kinase. Jpn J. Cancer Res. 76, 672-675
-
(1985)
Jpn J. Cancer Res.
, vol.76
, pp. 672-675
-
-
Uehara, Y.1
Hori, M.2
Takeuchi, T.3
Umezawa, H.4
-
10
-
-
0018702929
-
Inhibition of the transformation-specific kinase in ASV-transformed cells by N-α-tosyl-L-lysyl chloromethyl ketone
-
Richert, N., Davies, P. J., Jay, G. and Pastan, I. (1979) Inhibition of the transformation-specific kinase in ASV-transformed cells by N-α-tosyl-L-lysyl chloromethyl ketone. Cell 18, 369-374
-
(1979)
Cell
, vol.18
, pp. 369-374
-
-
Richert, N.1
Davies, P.J.2
Jay, G.3
Pastan, I.4
-
11
-
-
0023940887
-
Inhibition of transforming activity of tyrosine kinase oncogenes by herbimycin A
-
Uehara, Y., Murakami, Y., Mizuno, S. and Kawai, S. (1988) Inhibition of transforming activity of tyrosine kinase oncogenes by herbimycin A. Virology 164, 294-298
-
(1988)
Virology
, vol.164
, pp. 294-298
-
-
Uehara, Y.1
Murakami, Y.2
Mizuno, S.3
Kawai, S.4
-
12
-
-
0024240990
-
Blocking of EGF-dependent cell proliferation by EGF receptor kinase inhibitors
-
Yaish, P., Gazit, A., Gilon, C. and Levitzki, A. (1988) Blocking of EGF-dependent cell proliferation by EGF receptor kinase inhibitors. Science 242, 933-935
-
(1988)
Science
, vol.242
, pp. 933-935
-
-
Yaish, P.1
Gazit, A.2
Gilon, C.3
Levitzki, A.4
-
13
-
-
0026648901
-
Selective interactions of transforming and normal abl proteins with ATP, tyrosine-copolymer substrates, and tyrphostins
-
Anafi, M., Gazit, A., Gilon, C., Ben-Neriah, Y. and Levitzki, A. (1992) Selective interactions of transforming and normal abl proteins with ATP, tyrosine-copolymer substrates, and tyrphostins. J. Biol. Chem. 267, 4518-4523
-
(1992)
J. Biol. Chem.
, vol.267
, pp. 4518-4523
-
-
Anafi, M.1
Gazit, A.2
Gilon, C.3
Ben-Neriah, Y.4
Levitzki, A.5
-
14
-
-
0034665713
-
Structural mechanism for STI-571 inhibition of abelson tyrosine kinase
-
Schindler, T., Bornmann, W., Pellicena, P., Miller, W. T., Clarkson, B. and Kuriyan, J. (2000) Structural mechanism for STI-571 inhibition of abelson tyrosine kinase. Science 289, 1938-1942
-
(2000)
Science
, vol.289
, pp. 1938-1942
-
-
Schindler, T.1
Bornmann, W.2
Pellicena, P.3
Miller, W.T.4
Clarkson, B.5
Kuriyan, J.6
-
15
-
-
0033816156
-
Abl protein-tyrosine kinase inhibitor STI571 inhibits in vitro signal transduction mediated by c-kit and platelet-derived growth factor receptors
-
Buchdunger, E., Cioffi, C. L., Law, N. et al. (2000) Abl protein-tyrosine kinase inhibitor STI571 inhibits in vitro signal transduction mediated by c-kit and platelet-derived growth factor receptors. J. Pharmacol. Exp. Ther. 295, 139-145
-
(2000)
J. Pharmacol. Exp. Ther.
, vol.295
, pp. 139-145
-
-
Buchdunger, E.1
Cioffi, C.L.2
Law, N.3
-
16
-
-
0035871874
-
ARG tyrosine kinase activity is inhibited by STI571
-
Okuda, K., Weisberg, E., Gilliland, D. G. and Griffin, J. D. (2001) ARG tyrosine kinase activity is inhibited by STI571. Blood 97, 2440-2448
-
(2001)
Blood
, vol.97
, pp. 2440-2448
-
-
Okuda, K.1
Weisberg, E.2
Gilliland, D.G.3
Griffin, J.D.4
-
17
-
-
17044403497
-
Macrophage colony-stimulating factor receptor c-fms is a novel target of imatinib
-
Dewar, A. L., Cambareri, A. C., Zannettino, A. C. et al. (2005) Macrophage colony-stimulating factor receptor c-fms is a novel target of imatinib. Blood 105, 3127-3132
-
(2005)
Blood
, vol.105
, pp. 3127-3132
-
-
Dewar, A.L.1
Cambareri, A.C.2
Zannettino, A.C.3
-
19
-
-
0030853063
-
The tyrosine kinase inhibitor CGP57148B selectively inhibits the growth of BCR-ABL-positive cells
-
Deininger, M. W., Goldman, J. M., Lydon, N. and Melo, J. V. (1997) The tyrosine kinase inhibitor CGP57148B selectively inhibits the growth of BCR-ABL-positive cells. Blood 90, 3691-3698
-
(1997)
Blood
, vol.90
, pp. 3691-3698
-
-
Deininger, M.W.1
Goldman, J.M.2
Lydon, N.3
Melo, J.V.4
-
20
-
-
0022274007
-
IL-3-dependent mouse clones that express B-220 surface antigen, contain Ig genes in germ-line configuration, and generate B lymphocytes in vivo
-
Palacios, R. and Steinmetz, M. (1985) IL-3-dependent mouse clones that express B-220 surface antigen, contain Ig genes in germ-line configuration, and generate B lymphocytes in vivo. Cell 41, 727-734
-
(1985)
Cell
, vol.41
, pp. 727-734
-
-
Palacios, R.1
Steinmetz, M.2
-
21
-
-
0029947186
-
Effects of a selective inhibitor of the Abl tyrosine kinase on the growth of Bcr-Abl positive cells
-
Druker, B. J., Tamura, S., Buchdunger, E. et al. (1996) Effects of a selective inhibitor of the Abl tyrosine kinase on the growth of Bcr-Abl positive cells. Nat. Med. 2, 561-566
-
(1996)
Nat. Med.
, vol.2
, pp. 561-566
-
-
Druker, B.J.1
Tamura, S.2
Buchdunger, E.3
-
22
-
-
0030031766
-
Inhibition of the Abl protein-tyrosine kinase in vitro and in vivo by a 2-phenylaminopyrimidine derivative
-
Buchdunger, E., Zimmermann, J., Mett, H. et al. (1996) Inhibition of the Abl protein-tyrosine kinase in vitro and in vivo by a 2-phenylaminopyrimidine derivative. Cancer Res. 56, 100-104
-
(1996)
Cancer Res.
, vol.56
, pp. 100-104
-
-
Buchdunger, E.1
Zimmermann, J.2
Mett, H.3
-
23
-
-
30444446680
-
PKC412 inhibits in vitro growth of neoplastic human mast cells expressing the D816V-mutated variant of KIT: Comparison with AMN107, imatinib, and cladribine (2CdA) and evaluation of cooperative drug effects
-
Gleixner, K. V., Mayerhofer, M., Aichberger, K. J. et al. (2006) PKC412 inhibits in vitro growth of neoplastic human mast cells expressing the D816V-mutated variant of KIT: comparison with AMN107, imatinib, and cladribine (2CdA) and evaluation of cooperative drug effects. Blood 107, 752-759
-
(2006)
Blood
, vol.107
, pp. 752-759
-
-
Gleixner, K.V.1
Mayerhofer, M.2
Aichberger, K.J.3
-
24
-
-
24644464172
-
AMN107, a novel aminopyrimidine inhibitor of p190 Bcr-Abl activation and of in vitro proliferation of Philadelphia-positive acute lymphoblastic leukemia cells
-
Verstovsek, S., Golemovic, M., Kantarjian, H. et al. (2005) AMN107, a novel aminopyrimidine inhibitor of p190 Bcr-Abl activation and of in vitro proliferation of Philadelphia-positive acute lymphoblastic leukemia cells. Cancer 104, 1230-1236
-
(2005)
Cancer
, vol.104
, pp. 1230-1236
-
-
Verstovsek, S.1
Golemovic, M.2
Kantarjian, H.3
-
25
-
-
24644435728
-
AMN107, a novel aminopyrimidine inhibitor of Bcr-Abl, has in vitro activity against imatinib-resistant chronic myeloid leukemia
-
Golemovic, M., Verstovsek, S., Giles, F. et al. (2005) AMN107, a novel aminopyrimidine inhibitor of Bcr-Abl, has in vitro activity against imatinib-resistant chronic myeloid leukemia. Clin. Cancer Res. 11, 4941-4947
-
(2005)
Clin. Cancer Res.
, vol.11
, pp. 4941-4947
-
-
Golemovic, M.1
Verstovsek, S.2
Giles, F.3
-
26
-
-
13844251975
-
Characterization of AMN107, a selective inhibitor of native and mutant Bcr-Abl
-
Weisberg, E., Manley, P. W., Breitenstein, W. et al. (2005) Characterization of AMN107, a selective inhibitor of native and mutant Bcr-Abl. Cancer Cell 7, 129-141
-
(2005)
Cancer Cell
, vol.7
, pp. 129-141
-
-
Weisberg, E.1
Manley, P.W.2
Breitenstein, W.3
-
27
-
-
27144551665
-
The small molecule tyrosine kinase inhibitor AMN107 inhibits TEL-PDGFRβ and FIP1L1-PDGFRα in vitro and in vivo
-
Stover, E. H., Chen, J., Lee, B. H. et al. (2005) The small molecule tyrosine kinase inhibitor AMN107 inhibits TEL-PDGFRβ and FIP1L1-PDGFRα in vitro and in vivo. Blood 106, 3206-3213
-
(2005)
Blood
, vol.106
, pp. 3206-3213
-
-
Stover, E.H.1
Chen, J.2
Lee, B.H.3
-
28
-
-
31544459272
-
Dasatinib (BMS-354825), a dual SRC/ABL kinase inhibitor, inhibits the kinase activity of wild-type, juxtamembrane, and activation loop mutant KIT isoforms associated with human malignancies
-
Schittenhelm, M. M., Shiraga, S., Schroeder, A. et al. (2006) Dasatinib (BMS-354825), a dual SRC/ABL kinase inhibitor, inhibits the kinase activity of wild-type, juxtamembrane, and activation loop mutant KIT isoforms associated with human malignancies. Cancer Res. 66, 473-481
-
(2006)
Cancer Res.
, vol.66
, pp. 473-481
-
-
Schittenhelm, M.M.1
Shiraga, S.2
Schroeder, A.3
-
29
-
-
21144451094
-
In vitro activity of Bcr-Abl inhibitors AMN107 and BMS-354825 against clinically relevant imatinib-resistant Abl kinase domain mutants
-
O'hare, T., Walters, D. K., Stoffregen, E. P. et al. (2005) In vitro activity of Bcr-Abl inhibitors AMN107 and BMS-354825 against clinically relevant imatinib-resistant Abl kinase domain mutants. Cancer Res. 65, 4500-4505
-
(2005)
Cancer Res.
, vol.65
, pp. 4500-4505
-
-
O'Hare, T.1
Walters, D.K.2
Stoffregen, E.P.3
-
30
-
-
19944428353
-
Discovery of N-(2-chloro-6-methyl-phenyl)-2-(6-(4-(2-hydroxyethyl)- piperazin-1-yl)-2-methylpyrimidin-4-ylamino)thiazole-5-carboxamide (BMS-354825), a dual Src/Abl kinase inhibitor with potent antitumor activity in preclinical assays
-
Lombardo, L. J., Lee, F. Y., Chen, P. et al. (2004) Discovery of N-(2-chloro-6-methyl-phenyl)-2-(6-(4-(2-hydroxyethyl)-piperazin-1-yl) -2-methylpyrimidin-4-ylamino)thiazole-5-carboxamide (BMS-354825), a dual Src/Abl kinase inhibitor with potent antitumor activity in preclinical assays. J. Med. Chem. 47, 6658-6661
-
(2004)
J. Med. Chem.
, vol.47
, pp. 6658-6661
-
-
Lombardo, L.J.1
Lee, F.Y.2
Chen, P.3
-
31
-
-
13844261144
-
A non-ATP-competitive inhibitor of BCR-ABL overrides imatinib resistance
-
Gumireddy, K., Baker, S. J., Cosenza, S. C. et al. (2005) A non-ATP-competitive inhibitor of BCR-ABL overrides imatinib resistance. Proc. Natl. Acad. Sci. U.S.A. 102, 1992-1997
-
(2005)
Proc. Natl. Acad. Sci. U.S.A.
, vol.102
, pp. 1992-1997
-
-
Gumireddy, K.1
Baker, S.J.2
Cosenza, S.C.3
-
32
-
-
23344440655
-
Inhibition of drug-resistant mutants of ABL, KIT, and EGF receptor kinases
-
Carter, T. A., Wodicka, L. M., Shah, N. P. et al. (2005) Inhibition of drug-resistant mutants of ABL, KIT, and EGF receptor kinases. Proc. Natl. Acad. Sci. U.S.A. 102, 11011-11016
-
(2005)
Proc. Natl. Acad. Sci. U.S.A.
, vol.102
, pp. 11011-11016
-
-
Carter, T.A.1
Wodicka, L.M.2
Shah, N.P.3
-
33
-
-
22044443112
-
In vitro and in vivo activity of ATP-based kinase inhibitors AP23464 and AP23848 against activation-loop mutants of Kit
-
Corbin, A. S., Demehri, S., Griswold, I. J. et al. (2005) In vitro and in vivo activity of ATP-based kinase inhibitors AP23464 and AP23848 against activation-loop mutants of Kit. Blood 106, 227-234
-
(2005)
Blood
, vol.106
, pp. 227-234
-
-
Corbin, A.S.1
Demehri, S.2
Griswold, I.J.3
-
34
-
-
4644368478
-
Inhibition of wild-type and mutant Bcr-Abl by AP23464, a potent ATP-based oncogenic protein kinase inhibitor: Implications for CML
-
O'hare, T., Pollock, R., Stoffregen, E. P. et al. (2004) Inhibition of wild-type and mutant Bcr-Abl by AP23464, a potent ATP-based oncogenic protein kinase inhibitor: implications for CML. Blood 104, 2532-2539
-
(2004)
Blood
, vol.104
, pp. 2532-2539
-
-
O'Hare, T.1
Pollock, R.2
Stoffregen, E.P.3
-
35
-
-
26444442452
-
Combined Abl inhibitor therapy for minimizing drug resistance in chronic myeloid leukemia: Src/Abl inhibitors are compatible with imatinib
-
O'hare, T., Walters, D. K., Stoffregen, E. P. et al. (2005) Combined Abl inhibitor therapy for minimizing drug resistance in chronic myeloid leukemia: Src/Abl inhibitors are compatible with imatinib. Clin. Cancer Res. 11, 6987-6993
-
(2005)
Clin. Cancer Res.
, vol.11
, pp. 6987-6993
-
-
O'Hare, T.1
Walters, D.K.2
Stoffregen, E.P.3
-
36
-
-
0038813693
-
The Src-selective kinase inhibitor PP1 also inhibits Kit and Bcr-Abl tyrosine kinases
-
Tatton, L., Morley, G. M., Chopra, R. and Khwaja, A. (2003) The Src-selective kinase inhibitor PP1 also inhibits Kit and Bcr-Abl tyrosine kinases. J. Biol. Chem. 278, 4847-4853
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 4847-4853
-
-
Tatton, L.1
Morley, G.M.2
Chopra, R.3
Khwaja, A.4
-
37
-
-
0037438513
-
Dual-specific Src and Abl kinase inhibitors, PP1 and CGP76030, inhibit growth and survival of cells expressing imatinib mesylate-resistant Bcr-Abl kinases
-
Warmuth, M., Simon, N., Mitina, O. et al. (2003) Dual-specific Src and Abl kinase inhibitors, PP1 and CGP76030, inhibit growth and survival of cells expressing imatinib mesylate-resistant Bcr-Abl kinases. Blood 101, 664-672
-
(2003)
Blood
, vol.101
, pp. 664-672
-
-
Warmuth, M.1
Simon, N.2
Mitina, O.3
-
38
-
-
0037439689
-
SKI-606, a 4-anilino-3-quinolinecarbonitrile dual inhibitor of Src and Abl kinases, is a potent antiproliferative agent against chronic myelogenous leukemia cells in culture and causes regression of K562 xenografts in nude mice
-
Golas, J. M., Arndt, K., Etienne, C. et al. (2003) SKI-606, a 4-anilino-3-quinolinecarbonitrile dual inhibitor of Src and Abl kinases, is a potent antiproliferative agent against chronic myelogenous leukemia cells in culture and causes regression of K562 xenografts in nude mice. Cancer Res. 63, 375-381
-
(2003)
Cancer Res.
, vol.63
, pp. 375-381
-
-
Golas, J.M.1
Arndt, K.2
Etienne, C.3
-
39
-
-
28444479480
-
NS-187, a potent and selective dual Bcr-Abl/Lyn tyrosine kinase inhibitor, is a novel agent for imatinib-resistant leukemia
-
Kimura, S., Naito, H., Segawa, H. et al. (2005) NS-187, a potent and selective dual Bcr-Abl/Lyn tyrosine kinase inhibitor, is a novel agent for imatinib-resistant leukemia. Blood 106, 3948-3954
-
(2005)
Blood
, vol.106
, pp. 3948-3954
-
-
Kimura, S.1
Naito, H.2
Segawa, H.3
-
40
-
-
18544366598
-
PD166326, a novel tyrosine kinase inhibitor, has greater antileukemic activity than imatinib mesylate in a murine model of chronic myeloid leukemia
-
Wolff, N. C., Veach, D. R., Tong, W. P., Bornmann, W. G., Clarkson, B. and Ilaria, Jr, R. L. (2005) PD166326, a novel tyrosine kinase inhibitor, has greater antileukemic activity than imatinib mesylate in a murine model of chronic myeloid leukemia. Blood 105, 3995-4003
-
(2005)
Blood
, vol.105
, pp. 3995-4003
-
-
Wolff, N.C.1
Veach, D.R.2
Tong, W.P.3
Bornmann, W.G.4
Clarkson, B.5
Ilaria Jr., R.L.6
-
41
-
-
9444258068
-
Sensitivity of oncogenic KIT mutants to the kinase inhibitors MLN518 and PD180970
-
Corbin, A. S., Griswold, I. J., La, Rosee P. et al. (2004) Sensitivity of oncogenic KIT mutants to the kinase inhibitors MLN518 and PD180970. Blood 104, 3754-3757
-
(2004)
Blood
, vol.104
, pp. 3754-3757
-
-
Corbin, A.S.1
Griswold, I.J.2
La Rosee, P.3
-
42
-
-
0037115644
-
Activity of the Bcr-Abl kinase inhibitor PD180970 against clinically relevant Bcr-Abl isoforms that cause resistance to imatinib mesylate (Gleevec, STI571)
-
La, Rosee P., Corbin, A. S., Stoffregen, E. P., Deininger, M. W. and Druker, B. J. (2002) Activity of the Bcr-Abl kinase inhibitor PD180970 against clinically relevant Bcr-Abl isoforms that cause resistance to imatinib mesylate (Gleevec, STI571). Cancer Res. 62, 7149-7153
-
(2002)
Cancer Res.
, vol.62
, pp. 7149-7153
-
-
La Rosee, P.1
Corbin, A.S.2
Stoffregen, E.P.3
Deininger, M.W.4
Druker, B.J.5
-
43
-
-
15944378835
-
CHIR-258, a novel, multitargeted tyrosine kinase inhibitor for the potential treatment of t(4;14) multiple myeloma
-
Trudel, S., Li, Z. H., Wei, E. et al. (2005) CHIR-258, a novel, multitargeted tyrosine kinase inhibitor for the potential treatment of t(4;14) multiple myeloma. Blood 105, 2941-2948
-
(2005)
Blood
, vol.105
, pp. 2941-2948
-
-
Trudel, S.1
Li, Z.H.2
Wei, E.3
-
44
-
-
22344453138
-
CHIR-258: A potent inhibitor of FLT3 kinase in experimental tumor xenograft models of human acute myelogenous leukemia
-
Lopes de Menezes, D. E., Peng, J., Garrett, E. N. et al. (2005) CHIR-258: a potent inhibitor of FLT3 kinase in experimental tumor xenograft models of human acute myelogenous leukemia. Clin Cancer Res. 11, 5281-5291
-
(2005)
Clin Cancer Res.
, vol.11
, pp. 5281-5291
-
-
Lopes De Menezes, D.E.1
Peng, J.2
Garrett, E.N.3
-
45
-
-
1842420032
-
Single-agent CEP-701, a novel FLT3 inhibitor, shows biologic and clinical activity in patients with relapsed or refractory acute myeloid leukemia
-
Smith, B. D., Levis, M., Beran, M. et al. (2004) Single-agent CEP-701, a novel FLT3 inhibitor, shows biologic and clinical activity in patients with relapsed or refractory acute myeloid leukemia. Blood 103, 3669-3676
-
(2004)
Blood
, vol.103
, pp. 3669-3676
-
-
Smith, B.D.1
Levis, M.2
Beran, M.3
-
46
-
-
0037783433
-
A model of APL with FLT3 mutation is responsive to retinoic acid and a receptor tyrosine kinase inhibitor, SU11657
-
Sohal, J., Phan, V. T., Chan, P. V. et al. (2003) A model of APL with FLT3 mutation is responsive to retinoic acid and a receptor tyrosine kinase inhibitor, SU11657. Blood 101, 3188-3197
-
(2003)
Blood
, vol.101
, pp. 3188-3197
-
-
Sohal, J.1
Phan, V.T.2
Chan, P.V.3
-
47
-
-
3142515944
-
Complete remission of TEL-PDGFRB-induced myeloproliferative disease in mice by receptor tyrosine kinase inhibitor SU11657
-
Cain, J. A., Grisolano, J. L., Laird, A. D. and Tomasson, M. H. (2004) Complete remission of TEL-PDGFRB-induced myeloproliferative disease in mice by receptor tyrosine kinase inhibitor SU11657. Blood 104, 561-564
-
(2004)
Blood
, vol.104
, pp. 561-564
-
-
Cain, J.A.1
Grisolano, J.L.2
Laird, A.D.3
Tomasson, M.H.4
-
48
-
-
5144234541
-
PKC412 inhibits the zinc finger 198-fibroblast growth factor receptor 1 fusion tyrosine kinase and is active in treatment of stem cell myeloproliferative disorder
-
Chen, J., DeAngelo, D. J., Kutok, J. L. et al. (2004) PKC412 inhibits the zinc finger 198-fibroblast growth factor receptor 1 fusion tyrosine kinase and is active in treatment of stem cell myeloproliferative disorder. Proc. Natl. Acad. Sci. U.S.A. 101, 14479-14484
-
(2004)
Proc. Natl. Acad. Sci. U.S.A.
, vol.101
, pp. 14479-14484
-
-
Chen, J.1
Deangelo, D.J.2
Kutok, J.L.3
-
49
-
-
27144499798
-
Targeting FLT3 in primary MLL-gene-rearranged infant acute lymphoblastic leukemia
-
Stam, R. W., den Boer, M. L., Schneider, P. et al. (2005) Targeting FLT3 in primary MLL-gene-rearranged infant acute lymphoblastic leukemia. Blood 106, 2484-2490
-
(2005)
Blood
, vol.106
, pp. 2484-2490
-
-
Stam, R.W.1
Den Boer, M.L.2
Schneider, P.3
-
50
-
-
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. (2005) 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 105, 986-993
-
(2005)
Blood
, vol.105
, pp. 986-993
-
-
Fiedler, W.1
Serve, H.2
Dohner, H.3
-
51
-
-
10244277976
-
Synergistic effect of SU11248 with cytarabine or daunorubicin on FLT3 ITD-positive leukemic cells 1
-
Yee, K. W., Schittenhelm, M., O'Farrell, A. M. et al. (2004) Synergistic effect of SU11248 with cytarabine or daunorubicin on FLT3 ITD-positive leukemic cells 1. Blood 104, 4202-4209
-
(2004)
Blood
, vol.104
, pp. 4202-4209
-
-
Yee, K.W.1
Schittenhelm, M.2
O'Farrell, A.M.3
-
52
-
-
0141993064
-
A phase 2 clinical study of SU5416 in patients with refractory acute myeloid leukemia
-
Fiedler, W., Mesters, R., Tinnefeld, H. et al. (2003) A phase 2 clinical study of SU5416 in patients with refractory acute myeloid leukemia. Blood 102, 2763-2767
-
(2003)
Blood
, vol.102
, pp. 2763-2767
-
-
Fiedler, W.1
Mesters, R.2
Tinnefeld, H.3
-
53
-
-
7244251613
-
Variable sensitivity of FLT3 activation loop mutations to the small molecule tyrosine kinase inhibitor MLN518
-
Clark, J. J., Cools, J., Curley, D. P. et al. (2004) Variable sensitivity of FLT3 activation loop mutations to the small molecule tyrosine kinase inhibitor MLN518. Blood 104, 2867-2872
-
(2004)
Blood
, vol.104
, pp. 2867-2872
-
-
Clark, J.J.1
Cools, J.2
Curley, D.P.3
-
54
-
-
20844431698
-
Identification of Ki23819, a highly potent inhibitor of kinase activity of mutant FLT3 receptor tyrosine kinase
-
Komeno, Y., Kurokawa, M., Imai, Y. et al. (2005) Identification of Ki23819, a highly potent inhibitor of kinase activity of mutant FLT3 receptor tyrosine kinase. Leukemia 19, 930-935
-
(2005)
Leukemia
, vol.19
, pp. 930-935
-
-
Komeno, Y.1
Kurokawa, M.2
Imai, Y.3
-
55
-
-
33644889108
-
Allosteric inhibitors of Bcr-abl-dependent cell proliferation
-
Adrian, F. J., Ding, Q., Sim, T. et al. (2006) Allosteric inhibitors of Bcr-abl-dependent cell proliferation. Nat. Chem. Biol. 2, 95-102
-
(2006)
Nat. Chem. Biol.
, vol.2
, pp. 95-102
-
-
Adrian, F.J.1
Ding, Q.2
Sim, T.3
-
56
-
-
0035810147
-
Efficacy and safety of a specific inhibitor of the BCR-ABL tyrosine kinase in chronic myeloid leukemia
-
Druker, B. J., Talpaz, M., Resta, D. J. et al. (2001) Efficacy and safety of a specific inhibitor of the BCR-ABL tyrosine kinase in chronic myeloid leukemia. N. Engl. J. Med. 344, 1031-1037
-
(2001)
N. Engl. J. Med.
, vol.344
, pp. 1031-1037
-
-
Druker, B.J.1
Talpaz, M.2
Resta, D.J.3
-
57
-
-
0035810142
-
Activity of a specific inhibitor of the BCR-ABL tyrosine kinase in the blast crisis of chronic myeloid leukemia and acute lymphoblastic leukemia with the Philadelphia chromosome
-
Druker, B. J., Sawyers, C. L., Kantarjian, H. et al. (2001) Activity of a specific inhibitor of the BCR-ABL tyrosine kinase in the blast crisis of chronic myeloid leukemia and acute lymphoblastic leukemia with the Philadelphia chromosome. N. Engl. J. Med. 344, 1038-1042
-
(2001)
N. Engl. J. Med.
, vol.344
, pp. 1038-1042
-
-
Druker, B.J.1
Sawyers, C.L.2
Kantarjian, H.3
-
58
-
-
0035992329
-
Imatinib mesylate for Philadelphia chromosome-positive, chronic-phase myeloid leukemia after failure of interferon-α: Follow-up results
-
Kantarjian, H. M., Talpaz, M., O'Brien, S. et al. (2002) Imatinib mesylate for Philadelphia chromosome-positive, chronic-phase myeloid leukemia after failure of interferon-α: follow-up results. Clin. Cancer Res. 8, 2177-2187
-
(2002)
Clin. Cancer Res.
, vol.8
, pp. 2177-2187
-
-
Kantarjian, H.M.1
Talpaz, M.2
O'Brien, S.3
-
59
-
-
0037085785
-
Imatinib induces durable hematologic and cytogenetic responses in patients with accelerated phase chronic myeloid leukemia: Results of a phase 2 study
-
Talpaz, M., Silver, R. T., Druker, B. J. et al. (2002) Imatinib induces durable hematologic and cytogenetic responses in patients with accelerated phase chronic myeloid leukemia: results of a phase 2 study. Blood 99, 1928-1937
-
(2002)
Blood
, vol.99
, pp. 1928-1937
-
-
Talpaz, M.1
Silver, R.T.2
Druker, B.J.3
-
60
-
-
0037093092
-
Imatinib induces hematologic and cytogenetic responses in patients with chronic myelogenous leukemia in myeloid blast crisis: Results of a phase II study
-
Sawyers, C. L., Hochhaus, A., Feldman, E. et al. (2002) Imatinib induces hematologic and cytogenetic responses in patients with chronic myelogenous leukemia in myeloid blast crisis: results of a phase II study. Blood 99, 3530-3539
-
(2002)
Blood
, vol.99
, pp. 3530-3539
-
-
Sawyers, C.L.1
Hochhaus, A.2
Feldman, E.3
-
61
-
-
10744233716
-
Imatinib compared with interferon and low-dose cytarabine for newly diagnosed chronic-phase chronic myeloid leukemia
-
O'Brien, S. G., Guilhot, F., Larson, R. A. et al. (2003) Imatinib compared with interferon and low-dose cytarabine for newly diagnosed chronic-phase chronic myeloid leukemia. N. Engl. J. Med. 348, 994-1004
-
(2003)
N. Engl. J. Med.
, vol.348
, pp. 994-1004
-
-
O'Brien, S.G.1
Guilhot, F.2
Larson, R.A.3
-
62
-
-
33644538458
-
Beneficial effects of cytogenetic and molecular response on long-term outcome in patients with newly diagnosed chronic myeloid leukemia in chronic phase (CML-CP) treated with imatinib (IM): Update from the IRIS study
-
Simonsson, B. (2006) Beneficial effects of cytogenetic and molecular response on long-term outcome in patients with newly diagnosed chronic myeloid leukemia in chronic phase (CML-CP) treated with imatinib (IM): update from the IRIS study. Blood 106, 52a
-
(2006)
Blood
, vol.106
-
-
Simonsson, B.1
-
63
-
-
0035800507
-
Clinical resistance to STI-571 cancer therapy caused by BCR-ABL gene mutation or amplification
-
Gorre, M. E., Mohammed, M., Ellwood, K. et al. (2001) Clinical resistance to STI-571 cancer therapy caused by BCR-ABL gene mutation or amplification. Science 293, 876-880
-
(2001)
Science
, vol.293
, pp. 876-880
-
-
Gorre, M.E.1
Mohammed, M.2
Ellwood, K.3
-
64
-
-
9144234689
-
Imatinib mesylate resistance through BCR-ABL independence in chronic myelogenous leukemia
-
Donato, N. J., Wu, J. Y., Stapley, J. et al. (2004) Imatinib mesylate resistance through BCR-ABL independence in chronic myelogenous leukemia. Cancer Res. 64, 672-677
-
(2004)
Cancer Res.
, vol.64
, pp. 672-677
-
-
Donato, N.J.1
Wu, J.Y.2
Stapley, J.3
-
65
-
-
4344672552
-
Imatinib therapy in chronic myelogenous leukemia: Strategies to avoid and overcome resistance
-
Hochhaus, A. and La, Rosee P. (2004) Imatinib therapy in chronic myelogenous leukemia: strategies to avoid and overcome resistance. Leukemia 18, 1321-1331
-
(2004)
Leukemia
, vol.18
, pp. 1321-1331
-
-
Hochhaus, A.1
La Rosee, P.2
-
66
-
-
17844389113
-
New tyrosine kinase inhibitors in chronic myeloid leukemia
-
Martinelli, G., Soverini, S., Rosti, G., Cilloni, D. and Baccarani, M. (2005) New tyrosine kinase inhibitors in chronic myeloid leukemia. Haematologica 90, 534-541
-
(2005)
Haematologica
, vol.90
, pp. 534-541
-
-
Martinelli, G.1
Soverini, S.2
Rosti, G.3
Cilloni, D.4
Baccarani, M.5
-
67
-
-
13744251502
-
Targeting the silent minority: Emerging immunotherapeutic strategies for eradication of malignant stem cells in chronic myeloid leukaemia
-
Copland, M., Fraser, A. R., Harrison, S. J. and Holyoake, T. L. (2005) Targeting the silent minority: emerging immunotherapeutic strategies for eradication of malignant stem cells in chronic myeloid leukaemia. Cancer Immunol. Immunother. 54, 297-306
-
(2005)
Cancer Immunol. Immunother.
, vol.54
, pp. 297-306
-
-
Copland, M.1
Fraser, A.R.2
Harrison, S.J.3
Holyoake, T.L.4
-
68
-
-
0036683409
-
Overcoming STI571 resistance with the farnesyl transferase inhibitor SCH66336
-
Hoover, R. R., Mahon, F. X., Melo, J. V. and Daley, G. Q. (2002) Overcoming STI571 resistance with the farnesyl transferase inhibitor SCH66336. Blood 100, 1068-1071
-
(2002)
Blood
, vol.100
, pp. 1068-1071
-
-
Hoover, R.R.1
Mahon, F.X.2
Melo, J.V.3
Daley, G.Q.4
-
69
-
-
20144387198
-
Acquired resistance to imatinib in gastrointestinal stromal tumours caused by multiple KIT mutations
-
Wardelmann, E., Thomas, N., Merkelbach-Bruse, S. et al. (2005) Acquired resistance to imatinib in gastrointestinal stromal tumours caused by multiple KIT mutations. Lancet Oncol. 6, 249-251
-
(2005)
Lancet Oncol.
, vol.6
, pp. 249-251
-
-
Wardelmann, E.1
Thomas, N.2
Merkelbach-Bruse, S.3
-
70
-
-
13844317894
-
EGFR mutation and resistance of non-small-cell lung cancer to gefitinib
-
Kobayashi, S., Boggon, T. J., Dayaram, T. et al. (2005) EGFR mutation and resistance of non-small-cell lung cancer to gefitinib. N. Engl. J. Med. 352, 786-792
-
(2005)
N. Engl. J. Med.
, vol.352
, pp. 786-792
-
-
Kobayashi, S.1
Boggon, T.J.2
Dayaram, T.3
-
71
-
-
23844474533
-
A phase I study of BMS-354825 in patients with imatinib-resistant and intolerant accelerated and blast phase chronic myeloid leukemia (CML): Results from CA180002
-
Sawyers, C. L., Shah, N. P., Kantarjian, H. et al. (2005) A phase I study of BMS-354825 in patients with imatinib-resistant and intolerant accelerated and blast phase chronic myeloid leukemia (CML): Results from CA180002. J. Clin. Oncol. 23, 6520
-
(2005)
J. Clin. Oncol.
, vol.23
, pp. 6520
-
-
Sawyers, C.L.1
Shah, N.P.2
Kantarjian, H.3
-
72
-
-
29144511279
-
AMN107, a novel aminopyrimidine inhibitor of Bcr-Abl, has significant activity in imatinib-resistant bcr-abl positive chronic myeloid leukemia (CML)
-
Kantarjian, H., Ottmann, O. G., Cortes, J. et al. (2005) AMN107, a novel aminopyrimidine inhibitor of Bcr-Abl, has significant activity in imatinib-resistant bcr-abl positive chronic myeloid leukemia (CML). J. Clin. Oncol. 23, 3014
-
(2005)
J. Clin. Oncol.
, vol.23
, pp. 3014
-
-
Kantarjian, H.1
Ottmann, O.G.2
Cortes, J.3
-
73
-
-
23844515505
-
A phase I study of BMS-354825 in patients with imatinib-resistant and intolerant chronic phase chronic myeloid leukemia (CML): Results from CA180002
-
Talpaz, M., Kantarjian, H., Paquette, R. et al. (2005) A phase I study of BMS-354825 in patients with imatinib-resistant and intolerant chronic phase chronic myeloid leukemia (CML): Results from CA180002. J. Clin. Oncol. 23, 6519
-
(2005)
J. Clin. Oncol.
, vol.23
, pp. 6519
-
-
Talpaz, M.1
Kantarjian, H.2
Paquette, R.3
-
74
-
-
31344472945
-
Novel targeted therapies to overcome imatinib mesylate resistance in chronic myeloid leukemia (CML)
-
Walz, C. and Sattler, M. (2005) Novel targeted therapies to overcome imatinib mesylate resistance in chronic myeloid leukemia (CML). Crit. Rev. Oncol. Hematol. 57, 145-164
-
(2005)
Crit. Rev. Oncol. Hematol.
, vol.57
, pp. 145-164
-
-
Walz, C.1
Sattler, M.2
-
75
-
-
27244437924
-
New targeted approaches in chronic myeloid leukemia
-
Cortes, J. and Kantarjian, H. (2005) New targeted approaches in chronic myeloid leukemia. J. Clin. Oncol. 23, 6316-6324
-
(2005)
J. Clin. Oncol.
, vol.23
, pp. 6316-6324
-
-
Cortes, J.1
Kantarjian, H.2
-
76
-
-
29144464371
-
Advances in the structural biology, design and clinical development of Bcr-Abl kinase inhibitors for the treatment of chronic myeloid leukaemia
-
Manley, P. W., Cowan-Jacob, S. W. and Mestan, J. (2005) Advances in the structural biology, design and clinical development of Bcr-Abl kinase inhibitors for the treatment of chronic myeloid leukaemia. Biochim. Biophys. Acta 1754, 3-13
-
(2005)
Biochim. Biophys. Acta
, vol.1754
, pp. 3-13
-
-
Manley, P.W.1
Cowan-Jacob, S.W.2
Mestan, J.3
-
77
-
-
0037105560
-
A phase 2 study of imatimb in patients with relapsed or refractory Philadelphia chromosome-positive acute lymphoid leukemias
-
Ottmann, O. G., Druker, B. J., Sawyers, C. L. et al. (2002) A phase 2 study of imatimb in patients with relapsed or refractory Philadelphia chromosome-positive acute lymphoid leukemias. Blood 100, 1965-1971
-
(2002)
Blood
, vol.100
, pp. 1965-1971
-
-
Ottmann, O.G.1
Druker, B.J.2
Sawyers, C.L.3
-
78
-
-
26944439774
-
Clinical effect of imatinib added to intensive combination chemotherapy for newly diagnosed Philadelphia chromosome-positive acute lymphoblastic leukemia
-
Lee, K. H., Lee, J. H., Choi, S. J. et al. (2005) Clinical effect of imatinib added to intensive combination chemotherapy for newly diagnosed Philadelphia chromosome-positive acute lymphoblastic leukemia. Leukemia 19, 1509-1516
-
(2005)
Leukemia
, vol.19
, pp. 1509-1516
-
-
Lee, K.H.1
Lee, J.H.2
Choi, S.J.3
-
79
-
-
18244407767
-
The effect of first-line imatinib interim therapy on the outcome of allogeneic stem cell transplantation in adults with newly-diagnosed Philadelphia chromosome-positive acute lymphoblastic leukemia
-
Lee, S., Kim, Y. J., Min, C. K. et al. (2005) The effect of first-line imatinib interim therapy on the outcome of allogeneic stem cell transplantation in adults with newly-diagnosed Philadelphia chromosome-positive acute lymphoblastic leukemia. Blood 105, 3449-3457
-
(2005)
Blood
, vol.105
, pp. 3449-3457
-
-
Lee, S.1
Kim, Y.J.2
Min, C.K.3
-
80
-
-
33644845774
-
High complete remission rate and promising outcome by combination of imatinib and chemotherapy for newly-diagnosed BCR-ABL-positive acute lymphoblastic leukemia: A phase II study by the Japan Adult Leukemia Study Group
-
Yanada, M., Takeuchi, J., Sugiura, I. et al. (2006) High complete remission rate and promising outcome by combination of imatinib and chemotherapy for newly-diagnosed BCR-ABL-positive acute lymphoblastic leukemia: a phase II study by the Japan Adult Leukemia Study Group. J. Clin. Oncol. 24, 460-466
-
(2006)
J. Clin. Oncol.
, vol.24
, pp. 460-466
-
-
Yanada, M.1
Takeuchi, J.2
Sugiura, I.3
-
81
-
-
33748353278
-
Treatment of Philadelphia-positive acute lymphocytic leukemia (Ph+ ALL) in the elderly with imatinib mesylate (STI571) and Chemotherapy
-
Delannoy, A., Lheritier, V., Thomas, X. et al. (2005) Treatment of Philadelphia-positive acute lymphocytic leukemia (Ph+ ALL) in the elderly with imatinib mesylate (STI571) and Chemotherapy. Blood 106, 46a
-
(2005)
Blood
, vol.106
-
-
Delannoy, A.1
Lheritier, V.2
Thomas, X.3
-
82
-
-
33644506345
-
AMN107, a novel aminopyrimidine inhibitor of Bcr-Abl, has significant activity in imatinib-resistant chronic myeloid leukemia (CML) or Philadelphia-chromosome positive acute lymphoid leukemia (Ph+ ALL)
-
Kantarjian, H. M., Ottman, O., Corte, J. et al. (2006) AMN107, a novel aminopyrimidine inhibitor of Bcr-Abl, has significant activity in imatinib-resistant chronic myeloid leukemia (CML) or Philadelphia-chromosome positive acute lymphoid leukemia (Ph+ ALL). Blood 106, 15a-16a
-
(2006)
Blood
, vol.106
-
-
Kantarjian, H.M.1
Ottman, O.2
Corte, J.3
-
83
-
-
33644548543
-
Dasatinib (BMS-354825) in patients with chronic myeloid Leukemia (CML) and Philadelphia-chromosome positive acute lymphoblastic leukemia (Ph+ ALL) who are resistant or intolerant to imatinib: Update of a Phase I study
-
Sawyers, C. L., Kantarjian, H. M., Shah, N. P. et al. (2006) Dasatinib (BMS-354825) in patients with chronic myeloid Leukemia (CML) and Philadelphia-chromosome positive acute lymphoblastic leukemia (Ph+ ALL) who are resistant or intolerant to imatinib: update of a Phase I study. Blood 106, 16a
-
(2006)
Blood
, vol.106
-
-
Sawyers, C.L.1
Kantarjian, H.M.2
Shah, N.P.3
-
84
-
-
29144509820
-
Activity of AMN107, a novel aminopyrimidine inhibitor of Bcr-Abl, in imatimb-resistant bcr-abl positive lymphoid malignancies
-
Ottmann, O. G., Giles, F., Hochhaus, A. et al. (2005) Activity of AMN107, a novel aminopyrimidine inhibitor of Bcr-Abl, in imatimb-resistant bcr-abl positive lymphoid malignancies. J. Clin. Oncol. 23, 3015
-
(2005)
J. Clin. Oncol.
, vol.23
, pp. 3015
-
-
Ottmann, O.G.1
Giles, F.2
Hochhaus, A.3
-
85
-
-
0036566196
-
Transient response to imatinib mesylate (STI571) in a patient with the ETV6-ABL t(9;12) translocation
-
O'Brien, S. G., Vieira, S. A., Connors, S. et al. (2002) Transient response to imatinib mesylate (STI571) in a patient with the ETV6-ABL t(9;12) translocation. Blood 99, 3465-3467
-
(2002)
Blood
, vol.99
, pp. 3465-3467
-
-
O'Brien, S.G.1
Vieira, S.A.2
Connors, S.3
-
86
-
-
0038683894
-
Clinical and genetic studies of ETV6/ABL1-positive chronic myeloid leukaemia in blast crisis treated with imatinib mesylate
-
Barbouti, A., Ahlgren, T., Johansson, B. et al. (2003) Clinical and genetic studies of ETV6/ABL1-positive chronic myeloid leukaemia in blast crisis treated with imatinib mesylate. Br. J. Haematol. 122, 85-93
-
(2003)
Br. J. Haematol.
, vol.122
, pp. 85-93
-
-
Barbouti, A.1
Ahlgren, T.2
Johansson, B.3
-
87
-
-
12844278757
-
Molecular and cytogenetic characterization of a novel rearrangement involving chromosomes 9, 12, and 17 resulting in ETV6 (TEL) and ABL fusion
-
Tirado, C. A., Sebastian, S., Moore, J. O., Gong, J. Z. and Goodman, B. K. (2005) Molecular and cytogenetic characterization of a novel rearrangement involving chromosomes 9, 12, and 17 resulting in ETV6 (TEL) and ABL fusion. Cancer Genet. Cytogenet. 157, 74-77
-
(2005)
Cancer Genet. Cytogenet.
, vol.157
, pp. 74-77
-
-
Tirado, C.A.1
Sebastian, S.2
Moore, J.O.3
Gong, J.Z.4
Goodman, B.K.5
-
88
-
-
20844451217
-
Broad molecular screening of an unclassifiable myeloproliferative disorder reveals an unexpected ETV6/ABL1 fusion transcript
-
Meyer-Monard, S., Muhlematter, D., Streit, A. et al. (2005) Broad molecular screening of an unclassifiable myeloproliferative disorder reveals an unexpected ETV6/ABL1 fusion transcript. Leukemia 19, 1096-1099
-
(2005)
Leukemia
, vol.19
, pp. 1096-1099
-
-
Meyer-Monard, S.1
Muhlematter, D.2
Streit, A.3
-
89
-
-
20444378917
-
Fusion of EML1 to ABL1 in T-cell acute lymphoblastic leukemia with cryptic t(9;14)(q34;q32)
-
De Keersmaecker, K., Graux, C., Odero, M. D. et al. (2005) Fusion of EML1 to ABL1 in T-cell acute lymphoblastic leukemia with cryptic t(9;14)(q34;q32). Blood 105, 4849-4852
-
(2005)
Blood
, vol.105
, pp. 4849-4852
-
-
De Keersmaecker, K.1
Graux, C.2
Odero, M.D.3
-
90
-
-
6944252248
-
Fusion of NUP214 to ABL1 on amplified episomes in T-cell acute lymphoblastic leukemia
-
Graux, C., Cools, J., Melotte, C. et al. (2004) Fusion of NUP214 to ABL1 on amplified episomes in T-cell acute lymphoblastic leukemia. Nat. Genet. 36, 1084-1089
-
(2004)
Nat. Genet.
, vol.36
, pp. 1084-1089
-
-
Graux, C.1
Cools, J.2
Melotte, C.3
-
91
-
-
2942633624
-
Amplification of the ABL gene in T-cell acute lymphoblastic leukemia
-
Barber, K. E., Martineau, M., Harewood, L. et al. (2004) Amplification of the ABL gene in T-cell acute lymphoblastic leukemia. Leukemia 18, 1153-1156
-
(2004)
Leukemia
, vol.18
, pp. 1153-1156
-
-
Barber, K.E.1
Martineau, M.2
Harewood, L.3
-
92
-
-
26444600120
-
ABL1 amplification in T-cell acute lymphoblastic leukemia
-
Bernasconi, P., Calatroni, S., Giardini, I. et al. (2005) ABL1 amplification in T-cell acute lymphoblastic leukemia. Cancer Genet. Cytogenet. 162, 146-150
-
(2005)
Cancer Genet. Cytogenet.
, vol.162
, pp. 146-150
-
-
Bernasconi, P.1
Calatroni, S.2
Giardini, I.3
-
93
-
-
20144373994
-
NUP214-ABL1 amplification in t(5;14)/HOX11L2-positive ALL present with several forms and may have a prognostic significance
-
Ballerini, P., Busson, M., Fasola, S. et al. (2005) NUP214-ABL1 amplification in t(5;14)/HOX11L2-positive ALL present with several forms and may have a prognostic significance. Leukemia 19, 468-470
-
(2005)
Leukemia
, vol.19
, pp. 468-470
-
-
Ballerini, P.1
Busson, M.2
Fasola, S.3
-
94
-
-
26944431683
-
Fusion of NUP214 to ABL1 on amplified episomes in T-ALL: Implications for treatment
-
Stergianou, K., Fox, C. and Russell, N. H. (2005) Fusion of NUP214 to ABL1 on amplified episomes in T-ALL: implications for treatment. Leukemia 19, 1680-1681
-
(2005)
Leukemia
, vol.19
, pp. 1680-1681
-
-
Stergianou, K.1
Fox, C.2
Russell, N.H.3
-
95
-
-
0035823530
-
Case report: Rapid and complete control of idiopathic hypereosinophilia with imatinib mesylate
-
Schaller, J. L. and Burkland, G. A. (2001) Case report: rapid and complete control of idiopathic hypereosinophilia with imatinib mesylate. Med. Gen. Med. 3, 9
-
(2001)
Med. Gen. Med.
, vol.3
, pp. 9
-
-
Schaller, J.L.1
Burkland, G.A.2
-
96
-
-
0037018763
-
Treatment of hypereosinophilic syndrome with imatinib mesilate
-
Gleich, G. J., Leiferman, K. M., Pardanani, A., Tefferi, A. and Butterfield, J. H. (2002) Treatment of hypereosinophilic syndrome with imatinib mesilate. Lancet 359, 1577-1578
-
(2002)
Lancet
, vol.359
, pp. 1577-1578
-
-
Gleich, G.J.1
Leiferman, K.M.2
Pardanani, A.3
Tefferi, A.4
Butterfield, J.H.5
-
97
-
-
0344987881
-
A tyrosine kinase created by fusion of the PDGFRA and FIP1L1 genes as a therapeutic target of imatinib in idiopathic hypereosinophilic syndrome
-
Cools, J., DeAngelo, D. J., Gotlib, J. et al. (2003) A tyrosine kinase created by fusion of the PDGFRA and FIP1L1 genes as a therapeutic target of imatinib in idiopathic hypereosinophilic syndrome. N. Engl. J. Med. 348, 1201-1214
-
(2003)
N. Engl. J. Med.
, vol.348
, pp. 1201-1214
-
-
Cools, J.1
Deangelo, D.J.2
Gotlib, J.3
-
98
-
-
0037596569
-
Discovery of a fusion kinase in EOL-1 cells and idiopathic hypereosinophilic syndrome
-
Griffin, J. H., Leung, J., Bruner, R. J., Caligiuri, M. A. and Briesewitz, R. (2003) Discovery of a fusion kinase in EOL-1 cells and idiopathic hypereosinophilic syndrome. Proc. Natl. Acad. Sci. U.S.A. 100, 7830-7835
-
(2003)
Proc. Natl. Acad. Sci. U.S.A.
, vol.100
, pp. 7830-7835
-
-
Griffin, J.H.1
Leung, J.2
Bruner, R.J.3
Caligiuri, M.A.4
Briesewitz, R.5
-
99
-
-
8644263305
-
FIP1L1-PDGFRA fusion: Prevalence and clinicopathologic correlates in 89 consecutive patients with moderate to severe eosinophilia
-
Pardanani, A., Brockman, S. R., Paternoster, S. F. et al. (2004) FIP1L1-PDGFRA fusion: prevalence and clinicopathologic correlates in 89 consecutive patients with moderate to severe eosinophilia. Blood 104, 3038-3045
-
(2004)
Blood
, vol.104
, pp. 3038-3045
-
-
Pardanani, A.1
Brockman, S.R.2
Paternoster, S.F.3
-
100
-
-
0942276859
-
Molecular remission and reversal of myelofibrosis in response to imatinib mesylate treatment in patients with the myeloproliferative variant of hypereosinophilic syndrome
-
Klion, A. D., Robyn, J., Akin, C. et al. (2004) Molecular remission and reversal of myelofibrosis in response to imatinib mesylate treatment in patients with the myeloproliferative variant of hypereosinophilic syndrome. Blood 103, 473-478
-
(2004)
Blood
, vol.103
, pp. 473-478
-
-
Klion, A.D.1
Robyn, J.2
Akin, C.3
-
101
-
-
4243139496
-
Relationship between idiopathic hypereosinophilic syndrome, eosinophilic leukemia, and systemic mastocytosis
-
Bain, B. J. (2004) Relationship between idiopathic hypereosinophilic syndrome, eosinophilic leukemia, and systemic mastocytosis. Am. J. Hematol. 77, 82-85
-
(2004)
Am. J. Hematol.
, vol.77
, pp. 82-85
-
-
Bain, B.J.1
-
102
-
-
1842474941
-
The FIP1L1-PDGFRalpha fusion tyrosine kinase in hypereosinophilic syndrome and chronic eosinophilic leukemia: Implications for diagnosis, classification, and management
-
Gotlib, J., Cools, J., Malone, III, J. M., Schrier, S. L., Gilliland, D. G. and Coutre, S. E. (2004) The FIP1L1-PDGFRalpha fusion tyrosine kinase in hypereosinophilic syndrome and chronic eosinophilic leukemia: implications for diagnosis, classification, and management. Blood 103, 2879-2891
-
(2004)
Blood
, vol.103
, pp. 2879-2891
-
-
Gotlib, J.1
Cools, J.2
Malone III, J.M.3
Schrier, S.L.4
Gilliland, D.G.5
Coutre, S.E.6
-
103
-
-
33646532818
-
FIP1L1-PDGFRA in eosinophilic disorders: Prevalence in routine clinical practice, long-term experience with imatinib therapy, and a critical review of the literature
-
Pardanani, A., Ketterling, R. P., Li, C. Y. et al. (2006) FIP1L1-PDGFRA in eosinophilic disorders: prevalence in routine clinical practice, long-term experience with imatinib therapy, and a critical review of the literature. Leuk. Res. 30, 965-970
-
(2006)
Leuk. Res.
, vol.30
, pp. 965-970
-
-
Pardanani, A.1
Ketterling, R.P.2
Li, C.Y.3
-
104
-
-
2942548188
-
Imatinib mesylate can induce complete molecular remission in FIP1L1-PDGFR-a positive idiopathic hypereosinophilic syndrome
-
Martinelli, G., Malagola, M., Ottaviani, E., Rosti, G., Trabacchi, E. and Baccarani, M. (2004) Imatinib mesylate can induce complete molecular remission in FIP1L1-PDGFR-a positive idiopathic hypereosinophilic syndrome. Haematologica 89, 236-237
-
(2004)
Haematologica
, vol.89
, pp. 236-237
-
-
Martinelli, G.1
Malagola, M.2
Ottaviani, E.3
Rosti, G.4
Trabacchi, E.5
Baccarani, M.6
-
105
-
-
0142119964
-
PKC412 overcomes resistance to imatinib in a murine model of FIP1L1-PDGFRα-induced myeloproliferative disease
-
Cools, J., Stover, E. H., Boulton, C. L. et al. (2003) PKC412 overcomes resistance to imatinib in a murine model of FIP1L1-PDGFRα-induced myeloproliferative disease. Cancer Cell 3, 459-469
-
(2003)
Cancer Cell
, vol.3
, pp. 459-469
-
-
Cools, J.1
Stover, E.H.2
Boulton, C.L.3
-
106
-
-
29744466285
-
(6,7-Dimethoxy-2,4-dihydroindeno[1,2-c]pyrazol-3-yl)phenylamines: Platelet-derived growth factor receptor tyrosine kinase inhibitors with broad antiproliferative activity against tumor cells
-
Ho, C. Y., Ludovici, D. W., Maharoof, U. S. et al. (2005) (6,7-Dimethoxy-2,4-dihydroindeno[1,2-c]pyrazol-3-yl)phenylamines: platelet-derived growth factor receptor tyrosine kinase inhibitors with broad antiproliferative activity against tumor cells. J. Med. Chem. 48, 8163-8173
-
(2005)
J. Med. Chem.
, vol.48
, pp. 8163-8173
-
-
Ho, C.Y.1
Ludovici, D.W.2
Maharoof, U.S.3
-
107
-
-
0346186282
-
Novel translocations that disrupt the platelet-derived growth factor receptor beta (PDGFRB) gene in BCR-ABL-negative chronic myeloproliferative disorders
-
Baxter, E. J., Kulkarni, S., Vizmanos, J. L. et al. (2003) Novel translocations that disrupt the platelet-derived growth factor receptor beta (PDGFRB) gene in BCR-ABL-negative chronic myeloproliferative disorders. Br. J. Haematol. 120, 251-256
-
(2003)
Br. J. Haematol.
, vol.120
, pp. 251-256
-
-
Baxter, E.J.1
Kulkarni, S.2
Vizmanos, J.L.3
-
108
-
-
0041335547
-
Chronic myeloproliferative disorders with rearrangement of the platelet-derived growth factor α receptor: A new clinical target for STI571/Glivec
-
Trempat, P., Villalva, C., Laurent, G. et al. (2003) Chronic myeloproliferative disorders with rearrangement of the platelet-derived growth factor α receptor: a new clinical target for STI571/Glivec. Oncogene 22, 5702-5706
-
(2003)
Oncogene
, vol.22
, pp. 5702-5706
-
-
Trempat, P.1
Villalva, C.2
Laurent, G.3
-
109
-
-
1942453753
-
Molecular and cytogenetic characterization of a novel translocation t(4;22) involving the breakpoint cluster region and platelet-derived growth factor receptor-alpha genes in a patient with atypical chronic myeloid leukemia
-
Safley, A. M., Sebastian, S., Collins, T. S. et al. (2004) Molecular and cytogenetic characterization of a novel translocation t(4;22) involving the breakpoint cluster region and platelet-derived growth factor receptor-alpha genes in a patient with atypical chronic myeloid leukemia. Genes Chromosomes Cancer 40, 44-50
-
(2004)
Genes Chromosomes Cancer
, vol.40
, pp. 44-50
-
-
Safley, A.M.1
Sebastian, S.2
Collins, T.S.3
-
110
-
-
0028224348
-
Fusion of PDGF receptor beta to a novel ets-like gene, tel, in chronic myelomonocytic leukemia with t(5;12) chromosomal translocation
-
Golub, T. R., Barker, G. F., Lovett, M. and Gilliland, D. G. (1994) Fusion of PDGF receptor beta to a novel ets-like gene, tel, in chronic myelomonocytic leukemia with t(5;12) chromosomal translocation. Cell 77, 307-316
-
(1994)
Cell
, vol.77
, pp. 307-316
-
-
Golub, T.R.1
Barker, G.F.2
Lovett, M.3
Gilliland, D.G.4
-
111
-
-
0036202529
-
Myeloproliferative disorders with translocations of chromosome 5q31-5q35: Role of the platelet-derived growth factor receptor β
-
Steer, E. J. and Cross, N. C. (2002) Myeloproliferative disorders with translocations of chromosome 5q31-5q35: role of the platelet-derived growth factor receptor β. Acta Haematol. 107, 113-122
-
(2002)
Acta Haematol.
, vol.107
, pp. 113-122
-
-
Steer, E.J.1
Cross, N.C.2
-
112
-
-
0030669455
-
Fusion of the platelet-derived growth factor receptor beta to a novel gene CEV14 in acute myelogenous leukemia after clonal evolution
-
Abe, A., Emi, N., Tanimoto, M., Terasaki, H., Marunouchi, T. and Saito, H. (1997) Fusion of the platelet-derived growth factor receptor beta to a novel gene CEV14 in acute myelogenous leukemia after clonal evolution. Blood 90, 4271-4277
-
(1997)
Blood
, vol.90
, pp. 4271-4277
-
-
Abe, A.1
Emi, N.2
Tanimoto, M.3
Terasaki, H.4
Marunouchi, T.5
Saito, H.6
-
113
-
-
0031864246
-
Fusion of Huntingtin interacting protein 1 to platelet-derived growth factor β receptor (PDGFβR) in chronic myelomonocytic leukemia with t(5;7)(q33;q11.2)
-
Ross, T. S., Bernard, O. A., Berger, R. and Gilliland, D. G. (1998) Fusion of Huntingtin interacting protein 1 to platelet-derived growth factor β receptor (PDGFβR) in chronic myelomonocytic leukemia with t(5;7)(q33;q11.2). Blood 91, 4419-4426
-
(1998)
Blood
, vol.91
, pp. 4419-4426
-
-
Ross, T.S.1
Bernard, O.A.2
Berger, R.3
Gilliland, D.G.4
-
114
-
-
0038035638
-
Sensitivity to imatinib but low frequency of the TEL/PDGFRβ fusion protein in chronic myelomonocytic leukemia
-
Gunby, R. H., Cazzaniga, G., Tassi, E. et al. (2003) Sensitivity to imatinib but low frequency of the TEL/PDGFRβ fusion protein in chronic myelomonocytic leukemia. Haematologica 88, 408-415
-
(2003)
Haematologica
, vol.88
, pp. 408-415
-
-
Gunby, R.H.1
Cazzaniga, G.2
Tassi, E.3
-
115
-
-
18344404198
-
Fusion of H4/D10S170 to the platelet-derived growth factor receptor β in BCR-ABL-negative myeloproliferative disorders with a t(5;10)(q33;q21)
-
Kulkarni, S., Heath, C., Parker, S. et al. (2000) Fusion of H4/D10S170 to the platelet-derived growth factor receptor β in BCR-ABL-negative myeloproliferative disorders with a t(5;10)(q33;q21). Cancer Res. 60, 3592-3598
-
(2000)
Cancer Res.
, vol.60
, pp. 3592-3598
-
-
Kulkarni, S.1
Heath, C.2
Parker, S.3
-
116
-
-
0035877975
-
H4(D10S170), a gene frequently rearranged in papillary thyroid carcinoma, is fused to the platelet-derived growth factor receptor β gene in atypical chronic myeloid leukemia with t(5;10)(q33;q22)
-
Schwaller, J., Anastasiadou, E., Cain, D. et al. (2001) H4(D10S170), a gene frequently rearranged in papillary thyroid carcinoma, is fused to the platelet-derived growth factor receptor β gene in atypical chronic myeloid leukemia with t(5;10)(q33;q22). Blood 97, 3910-3918
-
(2001)
Blood
, vol.97
, pp. 3910-3918
-
-
Schwaller, J.1
Anastasiadou, E.2
Cain, D.3
-
117
-
-
0141816686
-
Imatinib mesylate elicits positive clinical response in atypical chronic myeloid leukemia involving the platelet-derived growth factor receptor β
-
Garcia, J. L., Font, de Mora, Hernandez, J. M. et al. (2003) Imatinib mesylate elicits positive clinical response in atypical chronic myeloid leukemia involving the platelet-derived growth factor receptor β. Blood 102, 2699-2700
-
(2003)
Blood
, vol.102
, pp. 2699-2700
-
-
Garcia, J.L.1
Font2
De Mora3
Hernandez, J.M.4
-
118
-
-
0035889128
-
Rabaptin-5 is a novel fusion partner to platelet-derived growth factor beta receptor in chronic myelomonocytic leukemia
-
Magnusson, M. K., Meade, K. E., Brown, K. E. et al. (2001) Rabaptin-5 is a novel fusion partner to platelet-derived growth factor beta receptor in chronic myelomonocytic leukemia. Blood 98, 2518-2525
-
(2001)
Blood
, vol.98
, pp. 2518-2525
-
-
Magnusson, M.K.1
Meade, K.E.2
Brown, K.E.3
-
119
-
-
0344826038
-
Cloning of the t(1;5)(q23;q33) in a myeloproliferative disorder associated with eosinophilia: Involvement of PDGFRB and response to imatinib
-
Wilkinson, K., Velloso, E. R., Lopes, L. F. et al. (2003) Cloning of the t(1;5)(q23;q33) in a myeloproliferative disorder associated with eosinophilia: involvement of PDGFRB and response to imatinib. Blood 102, 4187-4190
-
(2003)
Blood
, vol.102
, pp. 4187-4190
-
-
Wilkinson, K.1
Velloso, E.R.2
Lopes, L.F.3
-
120
-
-
11844290650
-
KIAA1509 is a novel PDGFRB fusion partner in imatinib-responsive myeloproliferative disease associated with a t(5;14)(q33;q32)
-
Levine, R. L., Wadleigh, M., Sternberg, D. W. et al. (2005) KIAA1509 is a novel PDGFRB fusion partner in imatinib-responsive myeloproliferative disease associated with a t(5;14)(q33;q32). Leukemia 19, 27-30
-
(2005)
Leukemia
, vol.19
, pp. 27-30
-
-
Levine, R.L.1
Wadleigh, M.2
Sternberg, D.W.3
-
121
-
-
5644271514
-
p53-binding protein 1 is fused to the platelet-derived growth factor receptor β in a patient with a t(5;15)(q33;q22) and an imatinib-responsive eosinophilic myeloproliferative disorder
-
Grand, F. H., Burgstaller, S., Ruhr, T. et al. (2004) p53-Binding protein 1 is fused to the platelet-derived growth factor receptor β in a patient with a t(5;15)(q33;q22) and an imatinib-responsive eosinophilic myeloproliferative disorder. Cancer Res. 64, 7216-7219
-
(2004)
Cancer Res.
, vol.64
, pp. 7216-7219
-
-
Grand, F.H.1
Burgstaller, S.2
Ruhr, T.3
-
122
-
-
5644284103
-
HCMOGT-1 is a novel fusion partner to PDGFRB in juvenile myelomonocytic leukemia with t(5;17)(q33;p11.2)
-
Morerio, C., Acquila, M., Rosanda, C. et al. (2004) HCMOGT-1 is a novel fusion partner to PDGFRB in juvenile myelomonocytic leukemia with t(5;17)(q33;p11.2). Cancer Res. 64, 2649-2651
-
(2004)
Cancer Res.
, vol.64
, pp. 2649-2651
-
-
Morerio, C.1
Acquila, M.2
Rosanda, C.3
-
123
-
-
5644251199
-
NIN, a gene encoding a CEP110-like centrosomal protein, is fused to PDGFRB in a patient with a t(5;14)(q33;q24) and an imatinib-responsive myeloproliferative disorder
-
Vizmanos, J. L., Novo, F. J., Roman, J. P. et al. (2004) NIN, a gene encoding a CEP110-like centrosomal protein, is fused to PDGFRB in a patient with a t(5;14)(q33;q24) and an imatinib-responsive myeloproliferative disorder. Cancer Res. 64, 2673-2676
-
(2004)
Cancer Res.
, vol.64
, pp. 2673-2676
-
-
Vizmanos, J.L.1
Novo, F.J.2
Roman, J.P.3
-
124
-
-
0031454003
-
CGP 57148, a tyrosine kinase inhibitor, inhibits the growth of cells expressing BCR-ABL, TEL-ABL, and TEL-PDGFR fusion proteins
-
Carroll, M., Ohno-Jones, S., Tamura, S. et al. (1997) CGP 57148, a tyrosine kinase inhibitor, inhibits the growth of cells expressing BCR-ABL, TEL-ABL, and TEL-PDGFR fusion proteins. Blood 90, 4947-4952
-
(1997)
Blood
, vol.90
, pp. 4947-4952
-
-
Carroll, M.1
Ohno-Jones, S.2
Tamura, S.3
-
125
-
-
0037103624
-
Response to imatinib mesylate in patients with chronic myeloproliferative diseases with rearrangements of the platelet-derived growth factor receptor β
-
Apperley, J. F., Gardembas, M., Melo, J. V. et al. (2002) Response to imatinib mesylate in patients with chronic myeloproliferative diseases with rearrangements of the platelet-derived growth factor receptor β. N. Engl. J. Med. 347, 481-487
-
(2002)
N. Engl. J. Med.
, vol.347
, pp. 481-487
-
-
Apperley, J.F.1
Gardembas, M.2
Melo, J.V.3
-
126
-
-
1342279448
-
A 2-year-old with atypical CML with a t(5;12)(q33;p13) treated successfully with imatinib mesylate
-
Wittman, B., Horan, J., Baxter, J. et al. (2004) A 2-year-old with atypical CML with a t(5;12)(q33;p13) treated successfully with imatinib mesylate. Leuk. Res. 28 (Suppl. 1), S65-S69
-
(2004)
Leuk. Res.
, vol.28
, Issue.SUPPL. 1
-
-
Wittman, B.1
Horan, J.2
Baxter, J.3
-
127
-
-
6344255327
-
Lack of response to imatinib mesylate in a patient with accelerated phase myeloproliferative disorder with rearrangement of the platelet-derived growth factor receptor β-gene
-
Bastie, J. N., Garcia, I., Terre, C., Cross, N. C., Mahon, F. X. and Castaigne, S. (2004) Lack of response to imatinib mesylate in a patient with accelerated phase myeloproliferative disorder with rearrangement of the platelet-derived growth factor receptor β-gene. Haematologica 89, 1263-1264
-
(2004)
Haematologica
, vol.89
, pp. 1263-1264
-
-
Bastie, J.N.1
Garcia, I.2
Terre, C.3
Cross, N.C.4
Mahon, F.X.5
Castaigne, S.6
-
128
-
-
0026760470
-
Differential inhibition of the epidermal growth factor-, platelet-derived growth factor-, and protein kinase C-mediated signal transduction pathways by the staurosporine derivative CGP 41251
-
Andrejauskas-Buchdunger, E. and Regenass, U. (1992) Differential inhibition of the epidermal growth factor-, platelet-derived growth factor-, and protein kinase C-mediated signal transduction pathways by the staurosporine derivative CGP 41251. Cancer Res. 52, 5353-5358
-
(1992)
Cancer Res.
, vol.52
, pp. 5353-5358
-
-
Andrejauskas-Buchdunger, E.1
Regenass, U.2
-
129
-
-
3042725365
-
Stable expression of small interfering RNA sensitizes TEL-PDGFβR to inhibition with imatinib or rapamycin
-
Chen, J., Wall, N. R., Kocher, K. et al. (2004) Stable expression of small interfering RNA sensitizes TEL-PDGFβR to inhibition with imatinib or rapamycin. J. Clin. Invest 113, 1784-1791
-
(2004)
J. Clin. Invest
, vol.113
, pp. 1784-1791
-
-
Chen, J.1
Wall, N.R.2
Kocher, K.3
-
130
-
-
0022626874
-
A new acute transforming feline retrovirus and relationship of its oncogene v-kit with the protein kinase gene family
-
Besmer, P., Murphy, J. E., George, P. C. et al. (1986) A new acute transforming feline retrovirus and relationship of its oncogene v-kit with the protein kinase gene family. Nature (London) 320, 415-421
-
(1986)
Nature (London)
, vol.320
, pp. 415-421
-
-
Besmer, P.1
Murphy, J.E.2
George, P.C.3
-
131
-
-
2742529418
-
Human proto-oncogene c-kit: A new cell surface receptor tyrosine kinase for an unidentified ligand
-
Yarden, Y., Kuang, W. J., Yang-Feng, T. et al. (1987) Human proto-oncogene c-kit: a new cell surface receptor tyrosine kinase for an unidentified ligand. EMBO J. 6, 3341-3351
-
(1987)
EMBO J.
, vol.6
, pp. 3341-3351
-
-
Yarden, Y.1
Kuang, W.J.2
Yang-Feng, T.3
-
132
-
-
0642368571
-
Kinase mutations and imatinib response in patients with metastatic gastrointestinal stromal tumor
-
Heinrich, M. C., Corless, C. L., Demetri, G. D. et al. (2003) Kinase mutations and imatinib response in patients with metastatic gastrointestinal stromal tumor. J. Clin. Oncol. 21, 4342-4349
-
(2003)
J. Clin. Oncol.
, vol.21
, pp. 4342-4349
-
-
Heinrich, M.C.1
Corless, C.L.2
Demetri, G.D.3
-
133
-
-
1542784354
-
KIT mutations are common in testicular seminomas
-
Kemmer, K., Corless, C. L., Fletcher, J. A. et al. (2004) KIT mutations are common in testicular seminomas. Am. J. Pathol. 164, 305-313
-
(2004)
Am. J. Pathol.
, vol.164
, pp. 305-313
-
-
Kemmer, K.1
Corless, C.L.2
Fletcher, J.A.3
-
134
-
-
0027359443
-
Identification of mutations in the coding sequence of the proto-oncogene c-kit in a human mast cell leukemia cell line causing ligand-independent activation of c-kit product
-
Furitsu, T., Tsujimura, T., Tono, T. et al. (1993) Identification of mutations in the coding sequence of the proto-oncogene c-kit in a human mast cell leukemia cell line causing ligand-independent activation of c-kit product. J. Clin. Invest. 92, 1736-1744
-
(1993)
J. Clin. Invest.
, vol.92
, pp. 1736-1744
-
-
Furitsu, T.1
Tsujimura, T.2
Tono, T.3
-
135
-
-
0028856070
-
Identification of a point mutation in the catalytic domain of the protooncogene c-kit in peripheral blood mononuclear cells of patients who have mastocytosis with an associated hematologic disorder
-
Nagata, H., Worobec, A. S., Oh, C. K. et al. (1995) Identification of a point mutation in the catalytic domain of the protooncogene c-kit in peripheral blood mononuclear cells of patients who have mastocytosis with an associated hematologic disorder. Proc. Natl. Acad. Sci. U.S.A. 92, 10560-10564
-
(1995)
Proc. Natl. Acad. Sci. U.S.A.
, vol.92
, pp. 10560-10564
-
-
Nagata, H.1
Worobec, A.S.2
Oh, C.K.3
-
136
-
-
13044305857
-
Activating and dominant inactivating c-KIT catalytic domain mutations in distinct clinical forms of human mastocytosis
-
Longley, Jr, B. J., Metcalfe, D. D., Tharp, M. et al. (1999) Activating and dominant inactivating c-KIT catalytic domain mutations in distinct clinical forms of human mastocytosis. Proc. Natl. Acad. Sci. U.S.A. 96, 1609-1614
-
(1999)
Proc. Natl. Acad. Sci. U.S.A.
, vol.96
, pp. 1609-1614
-
-
Longley Jr., B.J.1
Metcalfe, D.D.2
Tharp, M.3
-
137
-
-
21344465615
-
Clonality and molecular pathogenesis of mastocytosis
-
Akin, C. (2005) Clonality and molecular pathogenesis of mastocytosis. Acta Haematol. 114, 61-69
-
(2005)
Acta Haematol.
, vol.114
, pp. 61-69
-
-
Akin, C.1
-
138
-
-
1842579440
-
A novel form of mastocytosis associated with a transmembrane c-kit mutation and response to imatinib
-
Akin, C., Fumo, G., Yavuz, A. S., Lipsky, P. E., Neckers, L. and Metcalfe, D. D. (2004) A novel form of mastocytosis associated with a transmembrane c-kit mutation and response to imatinib. Blood 103, 3222-3225
-
(2004)
Blood
, vol.103
, pp. 3222-3225
-
-
Akin, C.1
Fumo, G.2
Yavuz, A.S.3
Lipsky, P.E.4
Neckers, L.5
Metcalfe, D.D.6
-
139
-
-
0031039992
-
A new c-kit mutation in a case of aggressive mast cell disease
-
Pignon, J. M., Giraudier, S., Duquesnoy, P. et al. (1997) A new c-kit mutation in a case of aggressive mast cell disease. Br. J. Haematol. 96, 374-376
-
(1997)
Br. J. Haematol.
, vol.96
, pp. 374-376
-
-
Pignon, J.M.1
Giraudier, S.2
Duquesnoy, P.3
-
140
-
-
24144503371
-
Novel germline mutation of KIT associated with familial gastrointestinal stromal tumors and mastocytosis
-
Hartmann, K., Wardelmann, E., Ma, Y. et al. (2005) Novel germline mutation of KIT associated with familial gastrointestinal stromal tumors and mastocytosis. Gastroenterology 129, 1042-1046
-
(2005)
Gastroenterology
, vol.129
, pp. 1042-1046
-
-
Hartmann, K.1
Wardelmann, E.2
Ma, Y.3
-
141
-
-
19444371824
-
A germline mutation in KIT in familial diffuse cutaneous mastocytosis
-
Tang, X., Boxer, M., Drummond, A., Ogston, P., Hodgins, M. and Burden, A. D. (2004) A germline mutation in KIT in familial diffuse cutaneous mastocytosis. J. Med. Genet. 41, e88
-
(2004)
J. Med. Genet.
, vol.41
-
-
Tang, X.1
Boxer, M.2
Drummond, A.3
Ogston, P.4
Hodgins, M.5
Burden, A.D.6
-
142
-
-
32844455834
-
A novel K509I mutation of KIT identified in familial mastocytosis: In vitro and in vivo responsiveness to imatinib therapy
-
Zhang, L. Y., Smith, M. L., Schultheis, B. et al. (2006) A novel K509I mutation of KIT identified in familial mastocytosis: in vitro and in vivo responsiveness to imatinib therapy. Leuk. Res. 30, 373-378
-
(2006)
Leuk. Res.
, vol.30
, pp. 373-378
-
-
Zhang, L.Y.1
Smith, M.L.2
Schultheis, B.3
-
143
-
-
27144506215
-
Activity of the tyrosine kinase inhibitor PKC412 in a patient with mast cell leukemia with the D816V KIT mutation
-
Gotlib, J., Berube, C., Growney, J. D. et al. (2005) Activity of the tyrosine kinase inhibitor PKC412 in a patient with mast cell leukemia with the D816V KIT mutation. Blood 106, 2865-2870
-
(2005)
Blood
, vol.106
, pp. 2865-2870
-
-
Gotlib, J.1
Berube, C.2
Growney, J.D.3
-
144
-
-
26944458584
-
The systemic mastocytosis-specific activating cKit mutation D816V can be inhibited by the tyrosine kinase inhibitor AMN107
-
von Bubnoff, N., Gorantla, S. H., Kancha, R. K., Lordick, F., Peschel, C. and Duyster, J. (2005) The systemic mastocytosis-specific activating cKit mutation D816V can be inhibited by the tyrosine kinase inhibitor AMN107. Leukemia 19, 1670-1671
-
(2005)
Leukemia
, vol.19
, pp. 1670-1671
-
-
Bubnoff, N.1
Gorantla, S.H.2
Kancha, R.K.3
Lordick, F.4
Peschel, C.5
Duyster, J.6
-
145
-
-
33645687784
-
D816V, an imatinib-resistant activating mutation that triggers neoplastic growth in the majority of patients with systemic mastocytosis
-
D816V, an imatinib-resistant activating mutation that triggers neoplastic growth in the majority of patients with systemic mastocytosis. Blood 108, 286-291
-
(2006)
Blood
, vol.108
, pp. 286-291
-
-
Shah, N.P.1
Lee, F.Y.2
Luo, R.3
Jiang, Y.4
Donker, M.5
Akin, C.6
-
146
-
-
22144455380
-
Activation mutations of human c-KIT resistant to imatinib mesylate are sensitive to the tyrosine kinase inhibitor PKC412
-
Growney, J. D., Clark, J. J., Adelsperger, J. et al. (2005) Activation mutations of human c-KIT resistant to imatinib mesylate are sensitive to the tyrosine kinase inhibitor PKC412. Blood 106, 721-724
-
(2005)
Blood
, vol.106
, pp. 721-724
-
-
Growney, J.D.1
Clark, J.J.2
Adelsperger, J.3
-
147
-
-
27144506215
-
Activity of the tyrosine kinase inhibitor PKC412 in a patient with mast cell leukemia with the D816V KIT mutation
-
Gotlib, J., Berube, C., Growney, J. D. et al. (2005) Activity of the tyrosine kinase inhibitor PKC412 in a patient with mast cell leukemia with the D816V KIT mutation. Blood 106, 2865-2870
-
(2005)
Blood
, vol.106
, pp. 2865-2870
-
-
Gotlib, J.1
Berube, C.2
Growney, J.D.3
-
148
-
-
0032989226
-
c-kit proto-oncogene exon 8 in-frame deletion plus insertion mutations in acute myeloid leukaemia
-
Gari, M., Goodeve, A., Wilson, G. et al. (1999) c-kit proto-oncogene exon 8 in-frame deletion plus insertion mutations in acute myeloid leukaemia. Br. J. Haematol. 105, 894-900
-
(1999)
Br. J. Haematol.
, vol.105
, pp. 894-900
-
-
Gari, M.1
Goodeve, A.2
Wilson, G.3
-
149
-
-
3943068350
-
KIT activating mutations: Incidence in adult and pediatric acute myeloid leukemia, and identification of an internal tandem duplication
-
Beghini, A., Ripamonti, C. B., Cairoli, R. et al. (2004) KIT activating mutations: incidence in adult and pediatric acute myeloid leukemia, and identification of an internal tandem duplication. Haematologica 89, 920-925
-
(2004)
Haematologica
, vol.89
, pp. 920-925
-
-
Beghini, A.1
Ripamonti, C.B.2
Cairoli, R.3
-
150
-
-
33646432204
-
Prognostic impact of c-KIT mutations in core binding factor leukemias. An Italian retrospective study
-
Cairoli, R., Beghini, A., Grillo, G. et al. (2005) Prognostic impact of c-KIT mutations in core binding factor leukemias. an Italian retrospective study. Blood 107, 3463-3468
-
(2005)
Blood
, vol.107
, pp. 3463-3468
-
-
Cairoli, R.1
Beghini, A.2
Grillo, G.3
-
151
-
-
19944431253
-
AML1-ETO and C-KIT mutation/overexpression in t(8;21) leukemia: Implication in stepwise leukemogenesis and response to Gleevec
-
Wang, Y. Y., Zhou, G. B., Yin, T. et al. (2005) AML1-ETO and C-KIT mutation/overexpression in t(8;21) leukemia: implication in stepwise leukemogenesis and response to Gleevec. Proc. Natl. Acad. Sci. U.S.A. 102, 1104-1109
-
(2005)
Proc. Natl. Acad. Sci. U.S.A.
, vol.102
, pp. 1104-1109
-
-
Wang, Y.Y.1
Zhou, G.B.2
Yin, T.3
-
152
-
-
23744498520
-
Mutations in the receptor tyrosine kinase pathway are associated with clinical outcome in patients with acute myeloblastic leukemia harboring t(8;21)(q22;q22)
-
Nanri, T., Matsuno, N., Kawakita, T. et al. (2005) Mutations in the receptor tyrosine kinase pathway are associated with clinical outcome in patients with acute myeloblastic leukemia harboring t(8;21)(q22;q22). Leukemia 19, 1361-1366
-
(2005)
Leukemia
, vol.19
, pp. 1361-1366
-
-
Nanri, T.1
Matsuno, N.2
Kawakita, T.3
-
153
-
-
0032104728
-
In vivo differentiation of mast cells from acute myeloid leukemia blasts carrying a novel activating ligand-independent C-kit mutation
-
Beghini, A., Cairoli, R., Morra, E. and Larizza, L. (1998) In vivo differentiation of mast cells from acute myeloid leukemia blasts carrying a novel activating ligand-independent C-kit mutation. Blood Cells Mol. Dis. 24, 262-270
-
(1998)
Blood Cells Mol. Dis.
, vol.24
, pp. 262-270
-
-
Beghini, A.1
Cairoli, R.2
Morra, E.3
Larizza, L.4
-
154
-
-
0033749308
-
Mast cell disease associated with acute myeloid leukemia: Detection of a new c-kit mutation Asp816His
-
Pullarkat, V. A., Pullarkat, S. T., Calverley, D. C. and Brynes, R. K. (2000) Mast cell disease associated with acute myeloid leukemia: detection of a new c-kit mutation Asp816His. Am. J. Hematol. 65, 307-309
-
(2000)
Am. J. Hematol.
, vol.65
, pp. 307-309
-
-
Pullarkat, V.A.1
Pullarkat, S.T.2
Calverley, D.C.3
Brynes, R.K.4
-
155
-
-
33344465478
-
KIT-D816 mutations in AML1-ETO-positive AML are associated with impaired event-free and overall survival
-
Schnittger, S., Kohl, T. M., Haferlach, T. et al. (2006) KIT-D816
-
(2006)
Blood
, vol.107
, pp. 1791-1799
-
-
Schnittger, S.1
Kohl, T.M.2
Haferlach, T.3
-
156
-
-
33344471932
-
KIT mutations, and not FLT3 internal tandem duplication, are strongly associated with a poor prognosis in pediatric acute myeloid leukemia with t(8;21): A study of the Japanese Childhood AML Cooperative Study Group
-
Shimada, A., Taki, T., Tabuchi, K. et al. (2006) KIT mutations, and not FLT3 internal tandem duplication, are strongly associated with a poor prognosis in pediatric acute myeloid leukemia with t(8;21): a study of the Japanese Childhood AML Cooperative Study Group. Blood 107, 1806-1809
-
(2006)
Blood
, vol.107
, pp. 1806-1809
-
-
Shimada, A.1
Taki, T.2
Tabuchi, K.3
-
157
-
-
2342518106
-
Efficacy and safety of imatinib in adult patients with c-kit-positive acute myeloid leukemia
-
Kindler, T., Breitenbuecher, F., Marx, A. et al. (2004) Efficacy and safety of imatinib in adult patients with c-kit-positive acute myeloid leukemia. Blood 103, 3644-3654
-
(2004)
Blood
, vol.103
, pp. 3644-3654
-
-
Kindler, T.1
Breitenbuecher, F.2
Marx, A.3
-
158
-
-
85117738549
-
Imatinib mesylate in the treatment of c-kit-positive acute myeloid leukemia: Is this the real target?
-
Malagola, M., Martinelli, G., Rondini, M. et al. (2005) Imatinib mesylate in the treatment of c-kit-positive acute myeloid leukemia: is this the real target? Blood 105, 904
-
(2005)
Blood
, vol.105
, pp. 904
-
-
Malagola, M.1
Martinelli, G.2
Rondini, M.3
-
159
-
-
13844275633
-
Imatinib mesylate in the treatment of core binding factor leukemias with KIT mutations: A report of three cases
-
Cairoli, R., Beghini, A., Morello, E. et al. (2005) Imatinib mesylate in the treatment of core binding factor leukemias with KIT mutations: a report of three cases. Leuk. Res. 29, 397-400
-
(2005)
Leuk. Res.
, vol.29
, pp. 397-400
-
-
Cairoli, R.1
Beghini, A.2
Morello, E.3
-
160
-
-
26944457435
-
Imatinib mesylate for refractory acute myeloblastic leukemia harboring inv(16) and a C-KIT exon 8 mutation
-
Nanri, T., Matsuno, N., Kawakita, T., Mitsuya, H. and Asou, N. (2005) Imatinib mesylate for refractory acute myeloblastic leukemia harboring inv(16) and a C-KIT exon 8 mutation. Leukemia 19, 1673-1675
-
(2005)
Leukemia
, vol.19
, pp. 1673-1675
-
-
Nanri, T.1
Matsuno, N.2
Kawakita, T.3
Mitsuya, H.4
Asou, N.5
-
161
-
-
0035412371
-
Stable remission after administration of the receptor tyrosine kinase inhibitor SU5416 in a patient with refractory acute myeloid leukemia
-
Mesters, R. M., Padro, T., Bieker, R. et al. (2001) Stable remission after administration of the receptor tyrosine kinase inhibitor SU5416 in a patient with refractory acute myeloid leukemia. Blood 98, 241-243
-
(2001)
Blood
, vol.98
, pp. 241-243
-
-
Mesters, R.M.1
Padro, T.2
Bieker, R.3
-
162
-
-
0037606031
-
Sustained complete hematologic remission after administration of the tyrosine kinase inhibitor imatinib mesylate in a patient with refractory, secondary AML
-
Kindler, T., Breitenbuecher, F., Marx, A. et al. (2003) Sustained complete hematologic remission after administration of the tyrosine kinase inhibitor imatinib mesylate in a patient with refractory, secondary AML. Blood 101, 2960-2962
-
(2003)
Blood
, vol.101
, pp. 2960-2962
-
-
Kindler, T.1
Breitenbuecher, F.2
Marx, A.3
-
163
-
-
17344373285
-
FGFR1 is fused with a novel zinc-finger gene, ZNF198, in the t(8;13) leukaemia/lymphoma syndrome
-
Xiao, S., Nalabolu, S. R., Aster, J. C. et al. (1998) FGFR1 is fused with a novel zinc-finger gene, ZNF198, in the t(8;13) leukaemia/lymphoma syndrome. Nat. Genet. 18, 84-87
-
(1998)
Nat. Genet.
, vol.18
, pp. 84-87
-
-
Xiao, S.1
Nalabolu, S.R.2
Aster, J.C.3
-
164
-
-
6844255886
-
The t(8;13)(p11;q11-q12) rearrangement associated with an atypical myeloproliferative disorder fuses the fibroblast growth factor receptor 1 gene to a novel gene RAMP
-
Smedley, D., Hamoudi, R., Clark, J. et al. (1998) The t(8;13)(p11;q11-q12) rearrangement associated with an atypical myeloproliferative disorder fuses the fibroblast growth factor receptor 1 gene to a novel gene RAMP. Hum. Mol. Genet. 7, 637-642
-
(1998)
Hum. Mol. Genet.
, vol.7
, pp. 637-642
-
-
Smedley, D.1
Hamoudi, R.2
Clark, J.3
-
165
-
-
0032510791
-
Fibroblast growth factor receptor 1 is fused to FIM in stem-cell myeloproliferative disorder with t(8;13)
-
Popovici, C., Adelaide, J., Ollendorff, V. et al. (1998) Fibroblast growth factor receptor 1 is fused to FIM in stem-cell myeloproliferative disorder with t(8;13). Proc. Natl. Acad. Sci. U.S.A. 95, 5712-5717
-
(1998)
Proc. Natl. Acad. Sci. U.S.A.
, vol.95
, pp. 5712-5717
-
-
Popovici, C.1
Adelaide, J.2
Ollendorff, V.3
-
166
-
-
0032170974
-
Consistent fusion of ZNF198 to the fibroblast growth factor receptor-1 in the t(8;13)(p11;q12) myeloproliferative syndrome
-
Reiter, A., Sohal, J., Kulkarni, S. et al. (1998) Consistent fusion of ZNF198 to the fibroblast growth factor receptor-1 in the t(8;13)(p11;q12) myeloproliferative syndrome. Blood 92, 1735-1742
-
(1998)
Blood
, vol.92
, pp. 1735-1742
-
-
Reiter, A.1
Sohal, J.2
Kulkarni, S.3
-
167
-
-
22344446662
-
Dual lympho-myeloproliferative disorder in a patient with t(8;22) with BCR-FGFR1 gene fusion
-
Murati, A., Arnoulet, C., Lafage-Pochitaloff, M. et al. (2005) Dual lympho-myeloproliferative disorder in a patient with t(8;22) with BCR-FGFR1 gene fusion. Int. J. Oncol. 26, 1485-1492
-
(2005)
Int. J. Oncol.
, vol.26
, pp. 1485-1492
-
-
Murati, A.1
Arnoulet, C.2
Lafage-Pochitaloff, M.3
-
168
-
-
0035159831
-
Fusion of the BCR and the fibroblast growth factor receptor-1 (FGFR1) genes as a result of t(8;22)(p11;q11) in a myeloproliferative disorder: The first fusion gene involving BCR but not ABL
-
Fioretos, T., Panagopoulos, I., Lassen, C. et al. (2001) Fusion of the BCR and the fibroblast growth factor receptor-1 (FGFR1) genes as a result of t(8;22)(p11;q11) in a myeloproliferative disorder: the first fusion gene involving BCR but not ABL. Genes Chromosomes Cancer 32, 302-310
-
(2001)
Genes Chromosomes Cancer
, vol.32
, pp. 302-310
-
-
Fioretos, T.1
Panagopoulos, I.2
Lassen, C.3
-
169
-
-
0036972521
-
A fourth case of BCR-FGFR1 positive CML-like disease with t(8;22) translocation showing an extensive deletion on the derivative chromosome 8p
-
Pini, M., Gottardi, E., Scaravaglio, P. et al. (2002) A fourth case of BCR-FGFR1 positive CML-like disease with t(8;22) translocation showing an extensive deletion on the derivative chromosome 8p. Hematol. J. 3, 315-316
-
(2002)
Hematol. J.
, vol.3
, pp. 315-316
-
-
Pini, M.1
Gottardi, E.2
Scaravaglio, P.3
-
170
-
-
19944432120
-
8p11 myeloproliferative syndrome with a novel t(7;8) translocation leading to fusion of the FGFR1 and TIF1 genes
-
Belloni, E., Trubia, M., Gasparini, P. et al. (2005) 8p11 myeloproliferative syndrome with a novel t(7;8) translocation leading to fusion of the FGFR1 and TIF1 genes. Genes Chromosomes Cancer 42, 320-325
-
(2005)
Genes Chromosomes Cancer
, vol.42
, pp. 320-325
-
-
Belloni, E.1
Trubia, M.2
Gasparini, P.3
-
171
-
-
20844443647
-
The t(8;17)(p11;q23) in the 8p11 myeloproliferative syndrome fuses MYO18A to FGFR1
-
Walz, C., Chase, A., Schoch, C. et al. (2005) The t(8;17)(p11;q23) in the 8p11 myeloproliferative syndrome fuses MYO18A to FGFR1. Leukemia 19, 1005-1009
-
(2005)
Leukemia
, vol.19
, pp. 1005-1009
-
-
Walz, C.1
Chase, A.2
Schoch, C.3
-
172
-
-
0034161335
-
FGFR1 is fused to the centrosome-associated protein CEP110 in the 8p12 stem cell myeloproliferative disorder with t(8;9)(p12;q33)
-
Guasch, G., Mack, G. J., Popovici, C. et al. (2000) FGFR1 is fused to the centrosome-associated protein CEP110 in the 8p12 stem cell myeloproliferative disorder with t(8;9)(p12;q33). Blood 95, 1788-1796
-
(2000)
Blood
, vol.95
, pp. 1788-1796
-
-
Guasch, G.1
Mack, G.J.2
Popovici, C.3
-
173
-
-
0033558253
-
The t(6;8)(q27;p11) translocation in a stem cell myeloproliferative disorder fuses a novel gene, FOP, to fibroblast growth factor receptor 1
-
Popovici, C., Zhang, B., Gregoire, M. J. et al. (1999) The t(6;8)(q27;p11) translocation in a stem cell myeloproliferative disorder fuses a novel gene, FOP, to fibroblast growth factor receptor 1. Blood 93, 1381-1389
-
(1999)
Blood
, vol.93
, pp. 1381-1389
-
-
Popovici, C.1
Zhang, B.2
Gregoire, M.J.3
-
174
-
-
11044238012
-
Clinical variability of patients with the t(6;8)(q27;p12) and FGFR1OP-FGFR1 fusion: Two further cases
-
Vizmanos, J. L., Hernandez, R., Vidal, M. J. et al. (2004) Clinical variability of patients with the t(6;8)(q27;p12) and FGFR1OP-FGFR1 fusion: two further cases. Hematol. J. 5, 534-537
-
(2004)
Hematol. J.
, vol.5
, pp. 534-537
-
-
Vizmanos, J.L.1
Hernandez, R.2
Vidal, M.J.3
-
175
-
-
1942422114
-
Identification of a novel gene, FGFR1OP2, fused to FGFR1 in the 8p11 myeloproliferative syndrome
-
Grand, E. K., Grand, F. H., Chase, A. J. et al. (2003) Identification of a novel gene, FGFR1OP2, fused to FGFR1 in the 8p11 myeloproliferative syndrome. Genes Chromosomes Cancer 40, 78-83
-
(2003)
Genes Chromosomes Cancer
, vol.40
, pp. 78-83
-
-
Grand, E.K.1
Grand, F.H.2
Chase, A.J.3
-
176
-
-
0037216062
-
Endogenous retroviral sequence is fused to FGFR1 kinase in the 8p12 stem-cell myeloproliferative disorder with t(8;19)(p12;q13.3)
-
Guasch, G., Popovici, C., Mugneret, F. et al. (2003) Endogenous retroviral sequence is fused to FGFR1 kinase in the 8p12 stem-cell myeloproliferative disorder with t(8;19)(p12;q13.3). Blood 101, 286-288
-
(2003)
Blood
, vol.101
, pp. 286-288
-
-
Guasch, G.1
Popovici, C.2
Mugneret, F.3
-
177
-
-
2342566403
-
Targeting FGFR3 in multiple myeloma: Inhibition of t(4;14)-positive cells by SU5402 and PD173074
-
Grand, E. K., Chase, A. J., Heath, C., Rahemtulla, A. and Cross, N. C. (2004) Targeting FGFR3 in multiple myeloma: inhibition of t(4;14)-positive cells by SU5402 and PD173074. Leukemia 18, 962-966
-
(2004)
Leukemia
, vol.18
, pp. 962-966
-
-
Grand, E.K.1
Chase, A.J.2
Heath, C.3
Rahemtulla, A.4
Cross, N.C.5
-
178
-
-
0036036768
-
A molecular study of the t(4;14) in multiple myeloma
-
Sibley, K., Fenton, J. A., Dring, A. M., Ashcroft, A. J., Rawstron, A. C. and Morgan, G. J. (2002) A molecular study of the t(4;14) in multiple myeloma. Br. J. Haematol. 118, 514-520
-
(2002)
Br. J. Haematol.
, vol.118
, pp. 514-520
-
-
Sibley, K.1
Fenton, J.A.2
Dring, A.M.3
Ashcroft, A.J.4
Rawstron, A.C.5
Morgan, G.J.6
-
179
-
-
0035577690
-
Fusion of ETV6 to fibroblast growth factor receptor 3 in peripheral T-cell lymphoma with a t(4;12)(p16;p13) chromosomal translocation
-
Yagasaki, F., Wakao, D., Yokoyama, Y. et al. (2001) Fusion of ETV6 to fibroblast growth factor receptor 3 in peripheral T-cell lymphoma with a t(4;12)(p16;p13) chromosomal translocation. Cancer Res. 61, 8371-8374
-
(2001)
Cancer Res.
, vol.61
, pp. 8371-8374
-
-
Yagasaki, F.1
Wakao, D.2
Yokoyama, Y.3
-
180
-
-
1542329588
-
Preclinical studies of fibroblast growth factor receptor 3 as a therapeutic target in multiple myeloma
-
Paterson, J. L., Li, Z., Wen, X. Y. et al. (2004) Preclinical studies of fibroblast growth factor receptor 3 as a therapeutic target in multiple myeloma. Br. J. Haematol. 124, 595-603
-
(2004)
Br. J. Haematol.
, vol.124
, pp. 595-603
-
-
Paterson, J.L.1
Li, Z.2
Wen, X.Y.3
-
181
-
-
31744438381
-
FGFR3 as a therapeutic target of the small molecule inhibitor PKC412 in hematopoietic malignancies
-
Chen, J., Lee, B. H., Williams, I. R. et al. (2005) FGFR3 as a therapeutic target of the small molecule inhibitor PKC412 in hematopoietic malignancies. Oncogene 24, 8259-8267
-
(2005)
Oncogene
, vol.24
, pp. 8259-8267
-
-
Chen, J.1
Lee, B.H.2
Williams, I.R.3
-
182
-
-
0030451722
-
Internal tandem duplication of the flt3 gene found in acute myeloid leukemia
-
Nakao, M., Yokota, S., Iwai, T. et al. (1996) Internal tandem duplication of the flt3 gene found in acute myeloid leukemia. Leukemia 10, 1911-1918
-
(1996)
Leukemia
, vol.10
, pp. 1911-1918
-
-
Nakao, M.1
Yokota, S.2
Iwai, T.3
-
183
-
-
0033134792
-
Prognostic implication of FLT3 and N-RAS gene mutations in acute myeloid leukemia
-
Kiyoi, H., Naoe, T., Nakano, Y. et al. (1999) Prognostic implication of FLT3 and N-RAS gene mutations in acute myeloid leukemia. Blood 93, 3074-3080
-
(1999)
Blood
, vol.93
, pp. 3074-3080
-
-
Kiyoi, H.1
Naoe, T.2
Nakano, Y.3
-
184
-
-
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, P. D., Gale, R. E., Frew, M. E. et al. (2001) 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 98, 1752-1759
-
(2001)
Blood
, vol.98
, pp. 1752-1759
-
-
Kottaridis, P.D.1
Gale, R.E.2
Frew, M.E.3
-
185
-
-
0035168677
-
Prevalence and prognostic significance of Flt3 internal tandem duplication in pediatric acute myeloid leukemia
-
Meshinchi, S., Woods, W. G., Stirewalt, D. L. et al. (2001) Prevalence and prognostic significance of Flt3 internal tandem duplication in pediatric acute myeloid leukemia. Blood 97, 89-94
-
(2001)
Blood
, vol.97
, pp. 89-94
-
-
Meshinchi, S.1
Woods, W.G.2
Stirewalt, D.L.3
-
186
-
-
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. (2002) 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 100, 59-66
-
(2002)
Blood
, vol.100
, pp. 59-66
-
-
Schnittger, S.1
Schoch, C.2
Dugas, M.3
-
187
-
-
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. (2002) Analysis of FLT3-activating mutations in 979 patients with acute myelogenous leukemia: association with FAB subtypes and identification of subgroups with poor prognosis. Blood 99, 4326-4335
-
(2002)
Blood
, vol.99
, pp. 4326-4335
-
-
Thiede, C.1
Steudel, C.2
Mohr, B.3
-
188
-
-
0034936404
-
Identification of novel FLT-3 Asp835 mutations in adult acute myeloid leukaemia
-
Abu-Duhier, F. M., Goodeve, A. C., Wilson, G. A., Care, R. S., Peake, I. R. and Reilly, J. T. (2001) Identification of novel FLT-3 Asp835 mutations in adult acute myeloid leukaemia. Br. J. Haematol. 113, 983-988
-
(2001)
Br. J. Haematol.
, vol.113
, 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
-
189
-
-
0035871889
-
Activating mutation of D835 within the activation loop of FLT3 in human hematologic malignancies
-
Yamamoto, Y., Kiyoi, H., Nakano, Y. et al. (2001) Activating mutation of D835 within the activation loop of FLT3 in human hematologic malignancies. Blood 97, 2434-2439
-
(2001)
Blood
, vol.97
, pp. 2434-2439
-
-
Yamamoto, Y.1
Kiyoi, H.2
Nakano, Y.3
-
190
-
-
1242315428
-
Novel FLT3 point mutations within exon 14 found in patients with acute myeloid leukaemia
-
Stirewalt, D. L., Meshinchi, S., Kussick, S. J. et al. (2004) Novel FLT3 point mutations within exon 14 found in patients with acute myeloid leukaemia. Br. J. Haematol. 124, 481-484
-
(2004)
Br. J. Haematol.
, vol.124
, pp. 481-484
-
-
Stirewalt, D.L.1
Meshinchi, S.2
Kussick, S.J.3
-
191
-
-
33645312560
-
Point mutations found in the juxtamembrane domain of FLT3 define a new class of activating mutations in AML
-
Reindl, C., Bagrintseva, K., Vempati, S. et al. (2006) Point mutations found in the juxtamembrane domain of FLT3 define a new class of activating mutations in AML. Blood 107, 3700-3709
-
(2006)
Blood
, vol.107
, pp. 3700-3709
-
-
Reindl, C.1
Bagrintseva, K.2
Vempati, S.3
-
192
-
-
33751284416
-
Favourable prognosis associated with FLT3 tyrosine kinase domain mutations in AML in contrast to the adverse outcome associated with internal tandem duplications
-
Mead, A., Linch, D., Hills, R., Wheatley, K., Burnett, A. K. and Gale, R. E. (2006) Favourable prognosis associated with FLT3 tyrosine kinase domain mutations in AML in contrast to the adverse outcome associated with internal tandem duplications. Blood 106, 101a
-
(2006)
Blood
, vol.106
-
-
Mead, A.1
Linch, D.2
Hills, R.3
Wheatley, K.4
Burnett, A.K.5
Gale, R.E.6
-
193
-
-
0345359585
-
An innovative phase I clinical study demonstrates inhibition of FLT3 phosphorylation by SU11248 in acute myeloid leukemia patients
-
O'Farrell, A. M., Foran, J. M., Fiedler, W. et al. (2003) An innovative phase I clinical study demonstrates inhibition of FLT3 phosphorylation by SU11248 in acute myeloid leukemia patients. Clin. Cancer Res. 9, 5465-5476
-
(2003)
Clin. Cancer Res.
, vol.9
, pp. 5465-5476
-
-
O'Farrell, A.M.1
Foran, J.M.2
Fiedler, W.3
-
194
-
-
22344453138
-
CHIR-258: A potent inhibitor of FLT3 kinase in experimental tumor xenograft models of human acute myelogenous leukemia
-
Lopes de Menezes, D. E., Peng, J., Garrett, E. N. et al. (2005) CHIR-258: a potent inhibitor of FLT3 kinase in experimental tumor xenograft models of human acute myelogenous leukemia. Clin Cancer Res. 11, 5281-5291
-
(2005)
Clin Cancer Res.
, vol.11
, pp. 5281-5291
-
-
Lopes De Menezes, D.E.1
Peng, J.2
Garrett, E.N.3
-
195
-
-
19944427559
-
Patients with acute myeloid leukemia and an activating mutation in FLT3 respond to a small-molecule FLT3 tyrosine kinase inhibitor, PKC412
-
Stone, R. M., DeAngelo, D. J., Klimek, V. et al. (2005) Patients with acute myeloid leukemia and an activating mutation in FLT3 respond to a small-molecule FLT3 tyrosine kinase inhibitor, PKC412. Blood 105, 54-60
-
(2005)
Blood
, vol.105
, pp. 54-60
-
-
Stone, R.M.1
Deangelo, D.J.2
Klimek, V.3
-
196
-
-
33747378382
-
Phase IB study of PKC412, an oral FLT3 kinase inhibitor, in sequential and simultaneous combinations with daunorubicin and cytarabine (DA) induction and high-dose cytarabine consolidation in newly diagnosed patients with AML
-
Stone, R., Fischer, T., Paquette, R. et al. (2006) Phase IB study of PKC412, an oral FLT3 kinase inhibitor, in sequential and simultaneous combinations with daunorubicin and cytarabine (DA) induction and high-dose cytarabine consolidation in newly diagnosed patients with AML. Blood 106, 121a-122a
-
(2006)
Blood
, vol.106
-
-
Stone, R.1
Fischer, T.2
Paquette, R.3
-
197
-
-
33747105356
-
A Randomized, open-label study of lestaurtinib (CEP-701), an oral FLT3 inhibitor, administered in sequence with chemotherapy in patients with relapsed AML harboring FLT3 activating mutations: Clinical response correlates with successful FLT3 inhibition
-
Levis, M., Smith, B. D., Beran, M. et al. (2006) A Randomized, open-label study of lestaurtinib (CEP-701), an oral FLT3 inhibitor, administered in sequence with chemotherapy in patients with relapsed AML harboring FLT3 activating mutations: clinical response correlates with successful FLT3 inhibition. Blood 106, 121a
-
(2006)
Blood
, vol.106
-
-
Levis, M.1
Smith, B.D.2
Beran, M.3
-
198
-
-
9144244169
-
FLT3 mutations in the activation loop of tyrosine kinase domain are frequently found in infant ALL with MLL rearrangements and pediatric ALL with hyperdiploidy
-
Taketani, T., Taki, T., Sugita, K. et al. (2004) FLT3 mutations in the activation loop of tyrosine kinase domain are frequently found in infant ALL with MLL rearrangements and pediatric ALL with hyperdiploidy. Blood 103, 1085-1088
-
(2004)
Blood
, vol.103
, pp. 1085-1088
-
-
Taketani, T.1
Taki, T.2
Sugita, K.3
-
199
-
-
0013312329
-
Inhibition of FLT3 in MLL. Validation of a therapeutic target identified by gene expression based classification
-
Armstrong, S. A., Kung, A. L., Mabon, M. E. et al. (2003) Inhibition of FLT3 in MLL. Validation of a therapeutic target identified by gene expression based classification. Cancer Cell 3, 173-183
-
(2003)
Cancer Cell
, vol.3
, pp. 173-183
-
-
Armstrong, S.A.1
Kung, A.L.2
Mabon, M.E.3
-
200
-
-
1542276560
-
FLT3 mutations in childhood acute lymphoblastic leukemia
-
Armstrong, S. A., Mabon, M. E., Silverman, L. B. et al. (2004) FLT3 mutations in childhood acute lymphoblastic leukemia. Blood 103, 3544-3546
-
(2004)
Blood
, vol.103
, pp. 3544-3546
-
-
Armstrong, S.A.1
Mabon, M.E.2
Silverman, L.B.3
-
201
-
-
3142512347
-
Activating FLT3 mutations in CD117/KIT(+) T-cell acute lymphoblastic leukemias
-
Paietta, E., Ferrando, A. A., Neuberg, D. et al. (2004) Activating FLT3 mutations in CD117/KIT(+) T-cell acute lymphoblastic leukemias. Blood 104, 558-560
-
(2004)
Blood
, vol.104
, pp. 558-560
-
-
Paietta, E.1
Ferrando, A.A.2
Neuberg, D.3
-
202
-
-
28844482915
-
Activating FLT3 mutations in CD4+/CD8-pediatric T-cell acute lymphoblastic leukemias
-
Van Vlierberghe, P., Meijerink, J. P., Stam, R. W. et al. (2005) Activating FLT3 mutations in CD4+/CD8-pediatric T-cell acute lymphoblastic leukemias. Blood 106, 4414-4415
-
(2005)
Blood
, vol.106
, pp. 4414-4415
-
-
Van Vlierberghe, P.1
Meijerink, J.P.2
Stam, R.W.3
-
203
-
-
17844383458
-
A unique clonal JAK2 mutation leading to constitutive signalling causes polycythaemia vera
-
James, C., Ugo, V., Le Couedic, J. P. et al. (2005) A unique clonal JAK2 mutation leading to constitutive signalling causes polycythaemia vera. Nature (London) 434, 1144-1148
-
(2005)
Nature (London)
, vol.434
, pp. 1144-1148
-
-
James, C.1
Ugo, V.2
Le Couedic, J.P.3
-
204
-
-
20144363192
-
Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders
-
Baxter, E. J., Scott, L. M., Campbell, P. J. et al. (2005) Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders. Lancet 365, 1054-1061
-
(2005)
Lancet
, vol.365
, pp. 1054-1061
-
-
Baxter, E.J.1
Scott, L.M.2
Campbell, P.J.3
-
205
-
-
20244369569
-
Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelofibrosis
-
Levine, R. L., Wadleigh, M., Cools, J. et al. (2005) Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelofibrosis. Cancer Cell 7. 387-397
-
(2005)
Cancer Cell
, vol.7
, pp. 387-397
-
-
Levine, R.L.1
Wadleigh, M.2
Cools, J.3
-
206
-
-
17644424955
-
A gain-of-function mutation of JAK2 in myeloproliferative disorders
-
Kralovics, R., Passamonti, F., Buser, A. S. et al. (2005) A gain-of-function mutation of JAK2 in myeloproliferative disorders. N. Engl. J. Med. 352, 1779-1790
-
(2005)
N. Engl. J. Med.
, vol.352
, pp. 1779-1790
-
-
Kralovics, R.1
Passamonti, F.2
Buser, A.S.3
-
207
-
-
20744460045
-
Identification of an acquired JAK2 mutation in Polycythemia vera
-
Zhao, R., Xing, S., Li, Z. et al. (2005) Identification of an acquired JAK2 mutation in Polycythemia vera. J. Biol. Chem. 280, 22788-22792
-
(2005)
J. Biol. Chem.
, vol.280
, pp. 22788-22792
-
-
Zhao, R.1
Xing, S.2
Li, Z.3
-
208
-
-
21344440357
-
The JAK2 V617F activating tyrosine kinase mutation is an infrequent event in both 'atypical' myeloproliferative disorders and the myelodysplastic syndrome
-
Steensma, D. P., Dewald, G. W., Lasho, T. L. et al. (2005) The JAK2 V617F activating tyrosine kinase mutation is an infrequent event in both 'atypical' myeloproliferative disorders and the myelodysplastic syndrome. Blood 106, 1207-1209
-
(2005)
Blood
, vol.106
, pp. 1207-1209
-
-
Steensma, D.P.1
Dewald, G.W.2
Lasho, T.L.3
-
209
-
-
21344467318
-
Widespread occurrence of the JAK2 V617F mutation in chronic myeloproliferative disorders
-
Jones, A. V., Kreil, S., Zoi, K. et al. (2005) Widespread occurrence of the JAK2 V617F mutation in chronic myeloproliferative disorders. Blood 106, 2162-2168
-
(2005)
Blood
, vol.106
, pp. 2162-2168
-
-
Jones, A.V.1
Kreil, S.2
Zoi, K.3
-
210
-
-
25844447519
-
JAK2 mutation 1849G>T is rare in acute leukemias but can be found in CMML, Philadelphia-chromosome negative CML and megakaryocytic leukemia
-
Jelinek, J., Oki, Y., Gharibyan, V. et al. (2005) JAK2 mutation 1849G>T is rare in acute leukemias but can be found in CMML, Philadelphia-chromosome negative CML and megakaryocytic leukemia. Blood 106, 3370-3373
-
(2005)
Blood
, vol.106
, pp. 3370-3373
-
-
Jelinek, J.1
Oki, Y.2
Gharibyan, V.3
-
211
-
-
9944248665
-
Janus kinase-3 (JAK3) inhibition: A novel immunosuppressive option for allogeneic transplantation
-
Saemann, M. D., Zeyda, M., Stulnig, T. M. et al. (2004) Janus kinase-3 (JAK3) inhibition: a novel immunosuppressive option for allogeneic transplantation. Transpl. Int. 17, 481-489
-
(2004)
Transpl. Int.
, vol.17
, pp. 481-489
-
-
Saemann, M.D.1
Zeyda, M.2
Stulnig, T.M.3
-
212
-
-
33645734511
-
Imatinib mesylate (GLEEVEC) is effective in the treatment of Polycythemia vera: A multi-institutional clinical trial
-
Silver, R. T., Fruchtman, S. M., Feldman, E., Spivak, J. L. and Salvado, A. J. (2004) Imatinib mesylate (GLEEVEC) is effective in the treatment of Polycythemia vera: a multi-institutional clinical trial. Blood 104, 4747a
-
(2004)
Blood
, vol.104
-
-
Silver, R.T.1
Fruchtman, S.M.2
Feldman, E.3
Spivak, J.L.4
Salvado, A.J.5
-
213
-
-
23844481514
-
Treatment of polycythemia vera with recombinant interferon α (rIFNα) or imatinib mesylate
-
Silver, R. T. (2005) Treatment of polycythemia vera with recombinant interferon α (rIFNα) or imatinib mesylate. Curr. Hematol. Rep. 4, 235-237
-
(2005)
Curr. Hematol. Rep.
, vol.4
, pp. 235-237
-
-
Silver, R.T.1
-
214
-
-
33645740979
-
Minimal molecular response in polycythemia vera patients treated with imatinib or interferon α
-
Jones, A. V., Silver, R. T., Waghorn, K. et al. (2006) Minimal molecular response in polycythemia vera patients treated with imatinib or interferon α. Blood 107, 3339-3341
-
(2006)
Blood
, vol.107
, pp. 3339-3341
-
-
Jones, A.V.1
Silver, R.T.2
Waghorn, K.3
-
215
-
-
15444339209
-
A TEL-JAK2 fusion protein with constitutive kinase activity in human leukemia
-
Lacronique, V., Boureux, A., Valle, V. D. et al. (1997) A TEL-JAK2 fusion protein with constitutive kinase activity in human leukemia. Science 278, 1309-1312
-
(1997)
Science
, vol.278
, pp. 1309-1312
-
-
Lacronique, V.1
Boureux, A.2
Valle, V.D.3
-
216
-
-
0030852328
-
Fusion of TEL, the ETS-variant gene 6 (ETV6), to the receptor-associated kinase JAK2 as a result of t(9;12) in a lymphoid and t(9;15;12) in a myeloid leukemia
-
Peeters, P., Raynaud, S. D., Cools, J. et al. (1997) Fusion of TEL, the ETS-variant gene 6 (ETV6), to the receptor-associated kinase JAK2 as a result of t(9;12) in a lymphoid and t(9;15;12) in a myeloid leukemia. Blood 90, 2535-2540
-
(1997)
Blood
, vol.90
, pp. 2535-2540
-
-
Peeters, P.1
Raynaud, S.D.2
Cools, J.3
-
217
-
-
25844469587
-
A BCR-JAK2 fusion gene as the result of a t(9;22)(p24;q11.2) translocation in a patient with a clinically typical chronic myeloid leukemia
-
Griesinger, F., Hennig, H., Hillmer, F. et al. (2005) A BCR-JAK2 fusion gene as the result of a t(9;22)(p24;q11.2) translocation in a patient with a clinically typical chronic myeloid leukemia. Genes Chromosomes Cancer 44, 329-333
-
(2005)
Genes Chromosomes Cancer
, vol.44
, pp. 329-333
-
-
Griesinger, F.1
Hennig, H.2
Hillmer, F.3
-
218
-
-
20144389913
-
The t(8;9)(p22;p24) is a recurrent abnormality in chronic and acute leukemia that fuses PCM1 to JAK2
-
Reiter, A., Walz, C., Watmore, A. et al. (2005) The t(8;9)(p22;p24) is a recurrent abnormality in chronic and acute leukemia that fuses PCM1 to JAK2. Cancer Res. 65, 2662-2667
-
(2005)
Cancer Res.
, vol.65
, pp. 2662-2667
-
-
Reiter, A.1
Walz, C.2
Watmore, A.3
-
219
-
-
27944481825
-
The t(8;9)(p22;p24) translocation in atypical chronic myeloid leukaemia yields a new PCM1-JAK2 fusion gene
-
Bousquet, M., Quelen, C., De Mas, V. et al. (2005) The t(8;9)(p22;p24) translocation in atypical chronic myeloid leukaemia yields a new PCM1-JAK2 fusion gene. Oncogene 24, 7248-7252
-
(2005)
Oncogene
, vol.24
, pp. 7248-7252
-
-
Bousquet, M.1
Quelen, C.2
De Mas, V.3
-
220
-
-
26944481210
-
PCM1-JAK2 fusion in myeloproliferative disorders and acute erythroid leukemia with t(8;9) translocation
-
Murati, A., Gelsi-Boyer, V., Adelaide, J. et al. (2005) PCM1-JAK2 fusion in myeloproliferative disorders and acute erythroid leukemia with t(8;9) translocation. Leukemia 19, 1692-1696
-
(2005)
Leukemia
, vol.19
, pp. 1692-1696
-
-
Murati, A.1
Gelsi-Boyer, V.2
Adelaide, J.3
-
221
-
-
33644552449
-
A t(8;9) translocation with PCM1-JAK2 fusion in a patient with T-cell lymphoma
-
Adelaide, J., Perot, C., Gelsi-Boyer, V. et al. (2006) A t(8;9) translocation with PCM1-JAK2 fusion in a patient with T-cell lymphoma. Leukemia 20, 536-537
-
(2006)
Leukemia
, vol.20
, pp. 536-537
-
-
Adelaide, J.1
Perot, C.2
Gelsi-Boyer, V.3
-
222
-
-
2342635959
-
Anaplastic lymphoma kinase proteins in growth control and cancer
-
Pulford, K., Morris, S. W. and Turturro, F. (2004) Anaplastic lymphoma kinase proteins in growth control and cancer. J. Cell. Physiol. 199, 330-358
-
(2004)
J. Cell. Physiol.
, vol.199
, pp. 330-358
-
-
Pulford, K.1
Morris, S.W.2
Turturro, F.3
-
223
-
-
0141705307
-
ALK activation by the CLTC-ALK fusion is a recurrent event in large B-cell lymphoma
-
De Paepe, P., Baens, M., van Krieken, H. et al. (2003) ALK activation by the CLTC-ALK fusion is a recurrent event in large B-cell lymphoma. Blood 102, 2638-2641
-
(2003)
Blood
, vol.102
, pp. 2638-2641
-
-
De Paepe, P.1
Baens, M.2
Van Krieken, H.3
-
224
-
-
0141705308
-
ALK-positive diffuse large B-cell lymphoma is associated with clathrin-ALK rearrangements: Report of 6 cases
-
Gascoyne, R. D., Lamant, L., Martin-Subero, J. I. et al. (2003) ALK-positive diffuse large B-cell lymphoma is associated with clathrin-ALK rearrangements: report of 6 cases. Blood 102, 2568-2573
-
(2003)
Blood
, vol.102
, pp. 2568-2573
-
-
Gascoyne, R.D.1
Lamant, L.2
Martin-Subero, J.I.3
-
225
-
-
0033890820
-
TPM3-ALK and TPM4-ALK oncogenes in inflammatory myofibroblastic tumors
-
Lawrence, B., Perez-Atayde, A., Hibbard, M. K. et al. (2000) TPM3-ALK and TPM4-ALK oncogenes in inflammatory myofibroblastic tumors. Am. J. Pathol. 157, 377-384
-
(2000)
Am. J. Pathol.
, vol.157
, pp. 377-384
-
-
Lawrence, B.1
Perez-Atayde, A.2
Hibbard, M.K.3
-
226
-
-
0041353435
-
A novel CLTC-TFE3 gene fusion in pediatric renal adenocarcinoma with t(X;17)(p11.2;q23)
-
Argani, P., Lui, M. Y., Couturier, J., Bouvier, R., Fournet, J. C. and Ladanyi, M. (2003) A novel CLTC-TFE3 gene fusion in pediatric renal adenocarcinoma with t(X;17)(p11.2;q23). Oncogene 22, 5374-5378
-
(2003)
Oncogene
, vol.22
, pp. 5374-5378
-
-
Argani, P.1
Lui, M.Y.2
Couturier, J.3
Bouvier, R.4
Fournet, J.C.5
Ladanyi, M.6
-
227
-
-
0037402562
-
Fusion of ALK to the Ran-binding protein 2 (RANBP2) gene in inflammatory myofibroblastic tumor
-
Ma, Z., Hill, D. A., Collins, M. H. et al. (2003) Fusion of ALK to the Ran-binding protein 2 (RANBP2) gene in inflammatory myofibroblastic tumor. Genes Chromosomes Cancer 37, 98-105
-
(2003)
Genes Chromosomes Cancer
, vol.37
, pp. 98-105
-
-
Ma, Z.1
Hill, D.A.2
Collins, M.H.3
-
228
-
-
0141701928
-
Identification of CARS-ALK fusion in primary and metastatic lesions of an inflammatory myofibroblastic tumor
-
Debelenko, L. V., Arthur, D. C., Pack, S. D., Helman, L. J., Schrump, D. S. and Tsokos, M. (2003) Identification of CARS-ALK fusion in primary and metastatic lesions of an inflammatory myofibroblastic tumor. Lab. Invest. 83, 1255-1265
-
(2003)
Lab. Invest.
, vol.83
, pp. 1255-1265
-
-
Debelenko, L.V.1
Arthur, D.C.2
Pack, S.D.3
Helman, L.J.4
Schrump, D.S.5
Tsokos, M.6
-
229
-
-
31844448139
-
Fusion of the SEC31L1 and ALK genes in an inflammatory myofibroblastic tumor
-
Panagopoulos, I., Nilsson, T., Domanski, H. A. et al. (2006) Fusion of the SEC31L1 and ALK genes in an inflammatory myofibroblastic tumor. Int. J. Cancer 118, 1181-1186
-
(2006)
Int. J. Cancer
, vol.118
, pp. 1181-1186
-
-
Panagopoulos, I.1
Nilsson, T.2
Domanski, H.A.3
-
230
-
-
23044468779
-
Antibody techniques used in the study of anaplastic lymphoma kinase-positive ALCL
-
Pulford, K., Roberton, H. M. and Jones, M. (2005) Antibody techniques used in the study of anaplastic lymphoma kinase-positive ALCL. Methods Mol. Med. 115, 271-294
-
(2005)
Methods Mol. Med.
, vol.115
, pp. 271-294
-
-
Pulford, K.1
Roberton, H.M.2
Jones, M.3
-
231
-
-
32644442671
-
Anaplastic lymphoma kinase activity is essential for the proliferation and survival of anaplastic large cell lymphoma cells
-
Wan, W., Albom, M. S., Lu, L. et al. (2005) Anaplastic lymphoma kinase activity is essential for the proliferation and survival of anaplastic large cell lymphoma cells. Blood 107, 1617-1623
-
(2005)
Blood
, vol.107
, pp. 1617-1623
-
-
Wan, W.1
Albom, M.S.2
Lu, L.3
-
232
-
-
19944434021
-
Identification of a SRC-like tyrosine kinase gene, FRK, fused with ETV6 in a patient with acute myelogenous leukemia carrying a t(6;12)(q21;p13) translocation
-
Hosoya, N., Qiao, Y., Hangaishi, A. et al. (2005) Identification of a SRC-like tyrosine kinase gene, FRK, fused with ETV6 in a patient with acute myelogenous leukemia carrying a t(6;12)(q21;p13) translocation. Genes Chromosomes Cancer 42, 269-279
-
(2005)
Genes Chromosomes Cancer
, vol.42
, pp. 269-279
-
-
Hosoya, N.1
Qiao, Y.2
Hangaishi, A.3
-
233
-
-
0025950015
-
Chromosomal translocations joining LCK and TCRB loci in human T cell leukemia
-
Tycko, B., Smith, S. D. and Sklar, J. (1991) Chromosomal translocations joining LCK and TCRB loci in human T cell leukemia. J. Exp. Med. 174, 867-873
-
(1991)
J. Exp. Med.
, vol.174
, pp. 867-873
-
-
Tycko, B.1
Smith, S.D.2
Sklar, J.3
-
234
-
-
0032778537
-
The tyrosine kinase abl-related gene ARG is fused to ETV6 in an AML-M4Eo patient with a t(1;12)(q25;p13): Molecular cloning of both reciprocal transcripts
-
Cazzaniga, G., Tosi, S., Aloisi, A. et al. (1999) The tyrosine kinase abl-related gene ARG is fused to ETV6 in an AML-M4Eo patient with a t(1;12)(q25;p13): molecular cloning of both reciprocal transcripts. Blood 94, 4370-4373
-
(1999)
Blood
, vol.94
, pp. 4370-4373
-
-
Cazzaniga, G.1
Tosi, S.2
Aloisi, A.3
-
235
-
-
17544386390
-
A new ETV6/TEL partner gene, ARG (ABL-related gene or ABL2), identified in an AML-M3 cell line with a t(1;12)(q25;p13) translocation
-
Iijima, Y., Ito, T., Oikawa, T. et al. (2000) A new ETV6/TEL partner gene, ARG (ABL-related gene or ABL2), identified in an AML-M3 cell line with a t(1;12)(q25;p13) translocation. Blood 95, 2126-2131
-
(2000)
Blood
, vol.95
, pp. 2126-2131
-
-
Iijima, Y.1
Ito, T.2
Oikawa, T.3
-
236
-
-
0036436878
-
Identification of an ETV6-ABL2 fusion transcript in combination with an ETV6 point mutation in a T-cell acute lymphoblastic leukaemia cell line
-
Griesinger, F., Janke, A., Podleschny, M. and Bohlander, S. K. (2002) Identification of an ETV6-ABL2 fusion transcript in combination with an ETV6 point mutation in a T-cell acute lymphoblastic leukaemia cell line. Br. J. Haematol. 119, 454-458
-
(2002)
Br. J. Haematol.
, vol.119
, pp. 454-458
-
-
Griesinger, F.1
Janke, A.2
Podleschny, M.3
Bohlander, S.K.4
-
237
-
-
31444450512
-
Novel t(5;9)(q33;q22) fuses ITK to SYK in unspecified peripheral T-cell lymphoma
-
Streubel, B., Vinatzer, U., Willheim, M., Raderer, M. and Chott, A. (2005) Novel t(5;9)(q33;q22) fuses ITK to SYK in unspecified peripheral T-cell lymphoma. Leukemia 20, 313-318
-
(2005)
Leukemia
, vol.20
, pp. 313-318
-
-
Streubel, B.1
Vinatzer, U.2
Willheim, M.3
Raderer, M.4
Chott, A.5
-
238
-
-
0035865603
-
Constitutive kinase activation of the TEL-Syk fusion gene in myelodysplastic syndrome with t(9;12)(q22;p12)
-
Kuno, Y., Abe, A., Emi, N. et al. (2001) Constitutive kinase activation of the TEL-Syk fusion gene in myelodysplastic syndrome with t(9;12)(q22;p12). Blood 97, 1050-1055
-
(2001)
Blood
, vol.97
, pp. 1050-1055
-
-
Kuno, Y.1
Abe, A.2
Emi, N.3
-
239
-
-
0033557864
-
Fusion of ETV6 to neurotrophin-3 receptor TRKC in acute myeloid leukemia with t(12;15)(p13;q25)
-
Eguchi, M., Eguchi-Ishimae, M., Tojo, A. et al. (1999) Fusion of ETV6 to neurotrophin-3 receptor TRKC in acute myeloid leukemia with t(12;15)(p13;q25). Blood 93, 1355-1363
-
(1999)
Blood
, vol.93
, pp. 1355-1363
-
-
Eguchi, M.1
Eguchi-Ishimae, M.2
Tojo, A.3
-
240
-
-
0031953233
-
A novel ETV6-NTRK3 gene fusion in congenital fibrosarcoma
-
Knezevich, S. R., McFadden, D. E., Tao, W., Lim, J. F. and Sorensen, P. H. (1998) A novel ETV6-NTRK3 gene fusion in congenital fibrosarcoma. Nat. Genet. 18, 184-187
-
(1998)
Nat. Genet.
, vol.18
, pp. 184-187
-
-
Knezevich, S.R.1
McFadden, D.E.2
Tao, W.3
Lim, J.F.4
Sorensen, P.H.5
-
241
-
-
0031738824
-
Congenital mesoblastic nephroma t(12;15) is associated with ETV6-NTRK3 gene fusion: Cytogenetic and molecular relationship to congenital (infantile) fibrosarcoma
-
Rubin, B. P., Chen, C. J., Morgan, T. W. et al. (1998) Congenital mesoblastic nephroma t(12;15) is associated with ETV6-NTRK3 gene fusion: cytogenetic and molecular relationship to congenital (infantile) fibrosarcoma. Am. J. Pathol. 153, 1451-1458
-
(1998)
Am. J. Pathol.
, vol.153
, pp. 1451-1458
-
-
Rubin, B.P.1
Chen, C.J.2
Morgan, T.W.3
-
242
-
-
19044391610
-
Expression of the ETV6-NTRK3 gene fusion as a primary event in human secretory breast carcinoma
-
Tognon, C., Knezevich, S. R., Huntsman, D. et al. (2002) Expression of the ETV6-NTRK3 gene fusion as a primary event in human secretory breast carcinoma. Cancer Cell 2, 367-376
-
(2002)
Cancer Cell
, vol.2
, pp. 367-376
-
-
Tognon, C.1
Knezevich, S.R.2
Huntsman, D.3
-
243
-
-
12744259891
-
Pediatric malignancies provide unique cancer therapy targets
-
Uren, A. and Toretsky, J. A. (2005) Pediatric malignancies provide unique cancer therapy targets. Curr. Opin. Pediatr. 17, 14-19
-
(2005)
Curr. Opin. Pediatr.
, vol.17
, pp. 14-19
-
-
Uren, A.1
Toretsky, J.A.2
-
244
-
-
12444324540
-
Potent small molecule inhibitors of spleen tyrosine kinase (Syk)
-
Lai, J. Y., Cox, P. J., Patel, R. et al. (2003) Potent small molecule inhibitors of spleen tyrosine kinase (Syk). Bioorg. Med. Chem. Lett. 13, 3111-3114
-
(2003)
Bioorg. Med. Chem. Lett.
, vol.13
, pp. 3111-3114
-
-
Lai, J.Y.1
Cox, P.J.2
Patel, R.3
-
245
-
-
33644851486
-
Genomic and expression profiling identifies the B-cell associated tyrosine kinase Syk as a possible therapeutic target in mantle cell lymphoma
-
Rinaldi, A., Kwee, I., Taborelli, M. et al. (2006) Genomic and expression profiling identifies the B-cell associated tyrosine kinase Syk as a possible therapeutic target in mantle cell lymphoma. Br. J. Haematol. 132, 303-316
-
(2006)
Br. J. Haematol.
, vol.132
, pp. 303-316
-
-
Rinaldi, A.1
Kwee, I.2
Taborelli, M.3
-
246
-
-
33750171885
-
Novel methods for the sensitive detection of c-KIT D816V and other exon 17 mutations in patients with mastocytosis
-
Tan, A. Y., Westerman, D. A., Lynch, K. P., Grant, A., McArthur, G. A. and Dobrovic, A. (2005) Novel methods for the sensitive detection of c-KIT D816V and other exon 17 mutations in patients with mastocytosis. Blood 106, 915a
-
(2005)
Blood
, vol.106
-
-
Tan, A.Y.1
Westerman, D.A.2
Lynch, K.P.3
Grant, A.4
McArthur, G.A.5
Dobrovic, A.6
|