-
1
-
-
0031008896
-
ALK, the chromosome 2 gene locus altered by the t(2;5) in non-Hodgkin's lymphoma, encodes a novel neural receptor tyrosine kinase that is highly related to leukocyte tyrosine kinase (LTK)
-
Morris, S. W.; Naeve, C.; Mathew, P.; James, P. L.; Kirstein, M. N.; Cui, X.; Witte, D. P. ALK, the chromosome 2 gene locus altered by the t(2;5) in non-Hodgkin's lymphoma, encodes a novel neural receptor tyrosine kinase that is highly related to leukocyte tyrosine kinase (LTK). Oncogene 1997, 14, 2175-2188.
-
(1997)
Oncogene
, vol.14
, pp. 2175-2188
-
-
Morris, S.W.1
Naeve, C.2
Mathew, P.3
James, P.L.4
Kirstein, M.N.5
Cui, X.6
Witte, D.P.7
-
2
-
-
0031035052
-
Molecular characterization of ALK, a receptor tyrosine kinase expressed specifically in the nervous system
-
Iwahara, T.; Fujimoto, J.; Wen, D.; Cupples, R.; Bucay, N.; Arakawa, T.; Mori, S.; Ratzkin, B.; Yamamoto, T. Molecular characterization of ALK, a receptor tyrosine kinase expressed specifically in the nervous system. Oncogene 1997, 14, 439-449.
-
(1997)
Oncogene
, vol.14
, pp. 439-449
-
-
Iwahara, T.1
Fujimoto, J.2
Wen, D.3
Cupples, R.4
Bucay, N.5
Arakawa, T.6
Mori, S.7
Ratzkin, B.8
Yamamoto, T.9
-
3
-
-
0028198206
-
Fusion of a kinase gene, ALK, to a nucleolar protein gene, NPM, in non- Hodgkin's lymphoma
-
Morris, S. W.; Kirstein, M. N.; Valentine, M. B.; Dittmer, K. G.; Shapiro, D. N.; Saltman, D. L.; Look, A. T. Fusion of a kinase gene, ALK, to a nucleolar protein gene, NPM, in non- Hodgkin's lymphoma. Science 1994, 263, 1281-1284.
-
(1994)
Science
, vol.263
, pp. 1281-1284
-
-
Morris, S.W.1
Kirstein, M.N.2
Valentine, M.B.3
Dittmer, K.G.4
Shapiro, D.N.5
Saltman, D.L.6
Look, A.T.7
-
4
-
-
0034761584
-
Anaplastic lymphoma kinase (ALK) expression in the inflammatory myofibroblastic tumor: A comparative immunohistochemical study
-
Cook, J. R.; Dehner, L. P.; Collins, M. H.; Ma, Z.; Morris, S. W.; Coffin, C. M.; Hill, D. A. Anaplastic lymphoma kinase (ALK) expression in the inflammatory myofibroblastic tumor: a comparative immunohistochemical study. Am. J. Surg. Pathol. 2001, 25, 1364-1371.
-
(2001)
Am. J. Surg. Pathol.
, vol.25
, pp. 1364-1371
-
-
Cook, J.R.1
Dehner, L.P.2
Collins, M.H.3
Ma, Z.4
Morris, S.W.5
Coffin, C.M.6
Hill, D.A.7
-
5
-
-
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.; Lestou, V. S.; Harris, N. L.; Muller-Hermelink, H. K.; Seymour, J. F.; Campbell, L. J.; Horsman, D. E.; Auvigne, I.; Espinos, E.; Siebert, R.; Delsol, G. ALK-positive diffuse large B-cell lymphoma is associated with Clathrin-ALK rearrangements: report of 6 cases. Blood 2003, 102, 2568-2573.
-
(2003)
Blood
, vol.102
, pp. 2568-2573
-
-
Gascoyne, R.D.1
Lamant, L.2
Martin-Subero, J.I.3
Lestou, V.S.4
Harris, N.L.5
Muller-Hermelink, H.K.6
Seymour, J.F.7
Campbell, L.J.8
Horsman, D.E.9
Auvigne, I.10
Espinos, E.11
Siebert, R.12
Delsol, G.13
-
6
-
-
0031755958
-
Nucleophosmin-anaplastic lymphoma kinase of large-cell anaplastic lymphoma is a constitutively active tyrosine kinase that utilizes phospholipase C-gamma to mediate its mitogenicity
-
Bai, R. Y.; Dieter, P.; Peschel, C.; Morris, S. W.; Duyster, J. Nucleophosmin-anaplastic lymphoma kinase of large-cell anaplastic lymphoma is a constitutively active tyrosine kinase that utilizes phospholipase C-gamma to mediate its mitogenicity. Mol. Cell. Biol. 1998, 18, 6951-6961.
-
(1998)
Mol. Cell. Biol.
, vol.18
, pp. 6951-6961
-
-
Bai, R.Y.1
Dieter, P.2
Peschel, C.3
Morris, S.W.4
Duyster, J.5
-
7
-
-
0035266314
-
Role of phosphatidylinositol 3-kinase-Akt pathway in nucleophosmin/ anaplastic lymphoma kinase-mediated lymphomagenesis
-
Slupianek, A.; Nieborowska-Skorska, M.; Hoser, G.; Morrione, A.; Majewski, M.; Xue, L.; Morris, S. W.; Wasik, M. A.; Skorski, T. Role of phosphatidylinositol 3-kinase-Akt pathway in nucleophosmin/anaplastic lymphoma kinase-mediated lymphomagenesis. Cancer Res. 2001, 61, 2194-2199.
-
(2001)
Cancer Res.
, vol.61
, pp. 2194-2199
-
-
Slupianek, A.1
Nieborowska-Skorska, M.2
Hoser, G.3
Morrione, A.4
Majewski, M.5
Xue, L.6
Morris, S.W.7
Wasik, M.A.8
Skorski, T.9
-
8
-
-
85047699293
-
Anaplastic lymphoma kinase (ALK) activates Stat3 and protects hematopoietic cells from cell death
-
Zamo, A.; Chiarle, R.; Piva, R.; Howes, J.; Fan, Y.; Chilosi, M.; Levy, D. E.; Inghirami, G. Anaplastic lymphoma kinase (ALK) activates Stat3 and protects hematopoietic cells from cell death. Oncogene 2002, 21, 1038-1047.
-
(2002)
Oncogene
, vol.21
, pp. 1038-1047
-
-
Zamo, A.1
Chiarle, R.2
Piva, R.3
Howes, J.4
Fan, Y.5
Chilosi, M.6
Levy, D.E.7
Inghirami, G.8
-
9
-
-
0030934862
-
Role of the nucleophosmin (NPM) portion of the non-Hodgkin's lymphoma-associated NPM-anaplastic lymphoma kinase fusion protein in oncogenesis
-
Bischof, D.; Pulford, K.; Mason, D. Y.; Morris, S. W. Role of the nucleophosmin (NPM) portion of the non-Hodgkin's lymphoma-associated NPM-anaplastic lymphoma kinase fusion protein in oncogenesis. Mol. Cell. Biol. 1997, 17, 2312-2325.
-
(1997)
Mol. Cell. Biol.
, vol.17
, pp. 2312-2325
-
-
Bischof, D.1
Pulford, K.2
Mason, D.Y.3
Morris, S.W.4
-
10
-
-
30444446194
-
Ablation of oncogenic ALK is a viable therapeutic approach for anaplastic large-cell lymphomas
-
Piva, R.; Chiarle, R.; Manazza, A. D.; Taulli, R.; Simmons, W.; Ambrogio, C.; D'Escamard, V.; Pellegrino, E.; Ponzetto, C.; Palestro, G.; Inghirami, G. Ablation of oncogenic ALK is a viable therapeutic approach for anaplastic large-cell lymphomas. Blood 2006, 107, 689-697.
-
(2006)
Blood
, vol.107
, pp. 689-697
-
-
Piva, R.1
Chiarle, R.2
Manazza, A.D.3
Taulli, R.4
Simmons, W.5
Ambrogio, C.6
D'Escamard, V.7
Pellegrino, E.8
Ponzetto, C.9
Palestro, G.10
Inghirami, G.11
-
11
-
-
21244497345
-
Anaplastic lymphoma kinase and its signaling molecules as novel targets in lymphoma therapy
-
Coluccia, A. M.; Gunby, R. H.; Tartari, C. J.; Scapozza, L.; Gambacorti-Passerini, C.; Passoni, L. Anaplastic lymphoma kinase and its signaling molecules as novel targets in lymphoma therapy. Expert Opin. Ther. Targets 2005, 9, 515-532.
-
(2005)
Expert Opin. Ther. Targets
, vol.9
, pp. 515-532
-
-
Coluccia, A.M.1
Gunby, R.H.2
Tartari, C.J.3
Scapozza, L.4
Gambacorti-Passerini, C.5
Passoni, L.6
-
12
-
-
15944404601
-
The development of imatinib as a therapeutic agent for chronic myeloid leukemia
-
Deininger, M.; Buchdunger, E.; Druker, B. J. The development of imatinib as a therapeutic agent for chronic myeloid leukemia. Blood 2005, 105, 2640-2653.
-
(2005)
Blood
, vol.105
, pp. 2640-2653
-
-
Deininger, M.1
Buchdunger, E.2
Druker, B.J.3
-
13
-
-
20044362947
-
State-of-the art therapy for gastrointestinal stromal tumors
-
Blanke, C. D.; Corless, C. L. State-of-the art therapy for gastrointestinal stromal tumors. Cancer Invest. 2005, 23, 274-280.
-
(2005)
Cancer Invest.
, vol.23
, pp. 274-280
-
-
Blanke, C.D.1
Corless, C.L.2
-
14
-
-
12144261476
-
Oncogenic derivatives of platelet-derived growth factor receptors
-
Jones, A. V.; Cross, N. C. Oncogenic derivatives of platelet-derived growth factor receptors. Cell. Mol. Life Sci. 2004, 61, 2912-2923.
-
(2004)
Cell. Mol. Life Sci.
, vol.61
, pp. 2912-2923
-
-
Jones, A.V.1
Cross, N.C.2
-
15
-
-
0034665713
-
Structural mechanism for STI-571 inhibition of abelson tyrosine kinase
-
Schindler, T.; Bornmann, W.; Pellicena, P.; Miller, W. T.; Clarkson, B.; Kuriyan, J. Structural mechanism for STI-571 inhibition of abelson tyrosine kinase. Science 2000, 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
-
16
-
-
0036682301
-
Crystal structures of the kinase domain of c-Abl in complex with the small molecule inhibitors PD173955 and imatinib (STI-571)
-
Nagar, B.; Bornmann, W. G.; Pellicena, P.; Schindler, T.; Veach, D. R.; Miller, W. T.; Clarkson, B.; Kuriyan, J. Crystal structures of the kinase domain of c-Abl in complex with the small molecule inhibitors PD173955 and imatinib (STI-571). Cancer Res. 2002, 62, 4236-4243.
-
(2002)
Cancer Res.
, vol.62
, pp. 4236-4243
-
-
Nagar, B.1
Bornmann, W.G.2
Pellicena, P.3
Schindler, T.4
Veach, D.R.5
Miller, W.T.6
Clarkson, B.7
Kuriyan, J.8
-
17
-
-
0035990893
-
Protein kinases as targets for anticancer agents: From inhibitors to useful drugs
-
Fabbro, D.; Ruetz, S.; Buchdunger, E.; Cowan-Jacob, S. W.; Fendrich, G.; Liebetanz, J.; Mestan, J.; O'Reilly, T.; Traxler, P.; Chaudhuri, B.; Fretz, H.; Zimmermann, J.; Meyer, T.; Caravatti, G.; Furet, P.; Manley, P. W. Protein kinases as targets for anticancer agents: from inhibitors to useful drugs. Pharmacol. Ther. 2002, 93, 79-98.
-
(2002)
Pharmacol. Ther.
, vol.93
, pp. 79-98
-
-
Fabbro, D.1
Ruetz, S.2
Buchdunger, E.3
Cowan-Jacob, S.W.4
Fendrich, G.5
Liebetanz, J.6
Mestan, J.7
O'Reilly, T.8
Traxler, P.9
Chaudhuri, B.10
Fretz, H.11
Zimmermann, J.12
Meyer, T.13
Caravatti, G.14
Furet, P.15
Manley, P.W.16
-
18
-
-
0032102902
-
Conversion of SB 203580-insensitive MAP kinase family members to drug-sensitive forms by a single amino acid substitution
-
Eyers, P. A.; Craxton, M.; Morrice, N.; Cohen, P.; Goedert, M. Conversion of SB 203580-insensitive MAP kinase family members to drug-sensitive forms by a single amino acid substitution. Chem. Biol. 1998, 5, 321-328.
-
(1998)
Chem. Biol.
, vol.5
, pp. 321-328
-
-
Eyers, P.A.1
Craxton, M.2
Morrice, N.3
Cohen, P.4
Goedert, M.5
-
19
-
-
0037674323
-
Mutation of threonine 766 in the epidermal growth factor receptor reveals a hotspot for resistance formation against selective tyrosine kinase inhibitors
-
Blencke, S.; Ullrich, A.; Daub, H. Mutation of threonine 766 in the epidermal growth factor receptor reveals a hotspot for resistance formation against selective tyrosine kinase inhibitors. J. Biol. Chem. 2003, 278, 15435-15440.
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 15435-15440
-
-
Blencke, S.1
Ullrich, A.2
Daub, H.3
-
20
-
-
2642558897
-
Characterization of a conserved structural determinant controlling protein kinase sensitivity to selective inhibitors
-
Blencke, S.; Zech, B.; Engkvist, O.; Greff, Z.; Orfi, L.; Horvath, Z.; Keri, G.; Ullrich, A.; Daub, H. Characterization of a conserved structural determinant controlling protein kinase sensitivity to selective inhibitors. Chem. Biol. 2004, 11, 691-701.
-
(2004)
Chem. Biol.
, vol.11
, pp. 691-701
-
-
Blencke, S.1
Zech, B.2
Engkvist, O.3
Greff, Z.4
Orfi, L.5
Horvath, Z.6
Keri, G.7
Ullrich, A.8
Daub, H.9
-
21
-
-
3042716081
-
A single amino acid exchange inverts susceptibility of related receptor tyrosine kinases for the ATP site inhibitor STI-571
-
Bohmer, F. D.; Karagyozov, L.; Uecker, A.; Serve, H.; Botzki, A.; Mahboobi, S.; Dove, S. A single amino acid exchange inverts susceptibility of related receptor tyrosine kinases for the ATP site inhibitor STI-571. J. Biol. Chem. 2003, 278, 5148-5155.
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 5148-5155
-
-
Bohmer, F.D.1
Karagyozov, L.2
Uecker, A.3
Serve, H.4
Botzki, A.5
Mahboobi, S.6
Dove, S.7
-
22
-
-
0035800507
-
Clinical resistance to STI-571 cancer therapy caused by BCR-ABL gene mutation or amplification
-
Gorre, M. E.; Mohammed, M.; Ellwood, K.; Hsu, N.; Paquette, R.; Rao, P. N.; Sawyers, C. L. Clinical resistance to STI-571 cancer therapy caused by BCR-ABL gene mutation or amplification. Science 2001, 293, 876-880.
-
(2001)
Science
, vol.293
, pp. 876-880
-
-
Gorre, M.E.1
Mohammed, M.2
Ellwood, K.3
Hsu, N.4
Paquette, R.5
Rao, P.N.6
Sawyers, C.L.7
-
23
-
-
0035576134
-
Three-dimensional model of the cyclin-dependent kinase 1 (CDK1): Ab initio active site parameters for molecular dynamics studies of CDKS
-
Cavalli, A.; Dezi, C.; Folkers, G.; Scapozza, L.; Recanatini, M. Three-dimensional model of the cyclin-dependent kinase 1 (CDK1): Ab initio active site parameters for molecular dynamics studies of CDKS. Proteins 2001, 45, 478-485.
-
(2001)
Proteins
, vol.45
, pp. 478-485
-
-
Cavalli, A.1
Dezi, C.2
Folkers, G.3
Scapozza, L.4
Recanatini, M.5
-
24
-
-
20544455834
-
3D-QSAR studies on c-Src kinase inhibitors and docking analyses of a potent dual kinase inhibitor of c-Src and c-Abl kinases
-
Thaimattam, R.; Daga, P. R.; Banerjee, R.; Iqbal, J. 3D-QSAR studies on c-Src kinase inhibitors and docking analyses of a potent dual kinase inhibitor of c-Src and c-Abl kinases. Bioorg. Med. Chem. 2005, 13, 4704-4712.
-
(2005)
Bioorg. Med. Chem.
, vol.13
, pp. 4704-4712
-
-
Thaimattam, R.1
Daga, P.R.2
Banerjee, R.3
Iqbal, J.4
-
25
-
-
0141953998
-
Inhibition of wild-type and mutant Bcr-Abl by pyrido-pyrimidine-type small molecule kinase inhibitors
-
von Bubnoff, N.; Veach, D. R.; Miller, W. T.; Li, W.; Sanger, J.; Peschel, C.; Bornmann, W. G.; Clarkson, B.; Duyster, J. Inhibition of wild-type and mutant Bcr-Abl by pyrido-pyrimidine-type small molecule kinase inhibitors. Cancer Res. 2003, 63, 6395-6404.
-
(2003)
Cancer Res.
, vol.63
, pp. 6395-6404
-
-
Bubnoff, N.1
Veach, D.R.2
Miller, W.T.3
Li, W.4
Sanger, J.5
Peschel, C.6
Bornmann, W.G.7
Clarkson, B.8
Duyster, J.9
-
26
-
-
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.; Lucas, J.; Nardin, D.; Gibbons, J.; Frost, P.; Ye, F.; Boschelli, D. H.; Boschelli, F. 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. 2003, 63, 375-381.
-
(2003)
Cancer Res.
, vol.63
, pp. 375-381
-
-
Golas, J.M.1
Arndt, K.2
Etienne, C.3
Lucas, J.4
Nardin, D.5
Gibbons, J.6
Frost, P.7
Ye, F.8
Boschelli, D.H.9
Boschelli, F.10
-
27
-
-
0036682230
-
Characterization of potent inhibitors of the Bcr-Abl and the c-kit receptor tyrosine kinases
-
Wisniewski, D.; Lambek, C. L.; Liu, C.; Strife, A.; Veach, D. R.; Nagar, B.; Young, M. A.; Schindler, T.; Bornmann, W. G.; Bertino, J. R.; Kuriyan, J.; Clarkson, B. Characterization of potent inhibitors of the Bcr-Abl and the c-kit receptor tyrosine kinases. Cancer Res. 2002, 62, 4244-4255.
-
(2002)
Cancer Res.
, vol.62
, pp. 4244-4255
-
-
Wisniewski, D.1
Lambek, C.L.2
Liu, C.3
Strife, A.4
Veach, D.R.5
Nagar, B.6
Young, M.A.7
Schindler, T.8
Bornmann, W.G.9
Bertino, J.R.10
Kuriyan, J.11
Clarkson, B.12
-
28
-
-
14744274624
-
Comparative analysis of two clinically active BCR-ABL kinase inhibitors reveals the role of conformation-specific binding in resistance
-
Burgess, M. R.; Skaggs, B. J.; Shah, N. P.; Lee, F. Y.; Sawyers, C. L. Comparative analysis of two clinically active BCR-ABL kinase inhibitors reveals the role of conformation-specific binding in resistance. Proc. Natl. Acad. Sci. U.S.A. 2005, 102, 3395-3400.
-
(2005)
Proc. Natl. Acad. Sci. U.S.A.
, vol.102
, pp. 3395-3400
-
-
Burgess, M.R.1
Skaggs, B.J.2
Shah, N.P.3
Lee, F.Y.4
Sawyers, C.L.5
-
29
-
-
0028582185
-
Crystal structure of the tyrosine kinase domain of the human insulin receptor
-
Hubbard, S. R.; Wei, L.; Ellis, L.; Hendrickson, W. A. Crystal structure of the tyrosine kinase domain of the human insulin receptor. Nature 1994, 372, 746-754.
-
(1994)
Nature
, vol.372
, pp. 746-754
-
-
Hubbard, S.R.1
Wei, L.2
Ellis, L.3
Hendrickson, W.A.4
-
30
-
-
0030766163
-
Crystal structure of the activated insulin receptor tyrosine kinase in complex with peptide substrate and ATP analogue
-
Hubbard, S. R. Crystal structure of the activated insulin receptor tyrosine kinase in complex with peptide substrate and ATP analogue. EMBO J. 1997, 16, 5572-5581.
-
(1997)
EMBO J.
, vol.16
, pp. 5572-5581
-
-
Hubbard, S.R.1
-
31
-
-
16144364951
-
Structural basis for activation of human lymphocyte kinase Lck upon tyrosine phosphorylation
-
Yamaguchi, H.; Hendrickson, W. A. Structural basis for activation of human lymphocyte kinase Lck upon tyrosine phosphorylation. Nature 1996, 384, 484-489.
-
(1996)
Nature
, vol.384
, pp. 484-489
-
-
Yamaguchi, H.1
Hendrickson, W.A.2
-
32
-
-
0030599010
-
A fast flexible docking method using an incremental construction algorithm
-
Rarey, M.; Kramer, B.; Lengauer, T.; Klebe, G. A fast flexible docking method using an incremental construction algorithm. J. Mol. Biol. 1996, 261, 470-489.
-
(1996)
J. Mol. Biol.
, vol.261
, pp. 470-489
-
-
Rarey, M.1
Kramer, B.2
Lengauer, T.3
Klebe, G.4
-
33
-
-
19944429284
-
A novel mode of Gleevec binding is revealed by the structure of spleen tyrosine kinase
-
Atwell, S.; Adams, J. M.; Badger, J.; Buchanan, M. D.; Feil, I. K.; Froning, K. J.; Gao, X.; Hendle, J.; Keegan, K.; Leon, B. C.; Muller-Dieckmann, H. J.; Nienaber, V. L.; Noland, B. W.; Post, K.; Rajashankar, K. R.; Ramos, A.; Russell, M.; Burley, S. K.; Buchanan, S. G. A novel mode of Gleevec binding is revealed by the structure of spleen tyrosine kinase. J. Biol. Chem. 2004, 279, 55827-55832.
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 55827-55832
-
-
Atwell, S.1
Adams, J.M.2
Badger, J.3
Buchanan, M.D.4
Feil, I.K.5
Froning, K.J.6
Gao, X.7
Hendle, J.8
Keegan, K.9
Leon, B.C.10
Muller-Dieckmann, H.J.11
Nienaber, V.L.12
Noland, B.W.13
Post, K.14
Rajashankar, K.R.15
Ramos, A.16
Russell, M.17
Burley, S.K.18
Buchanan, S.G.19
-
34
-
-
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.; Quail, M. R.; Becknell, N. C.; Weinberg, L. R.; Reddy, D. R.; Holskin, B. P.; Angeles, T. S.; Underiner, T. L.; Meyer, S. L.; Hudkins, R. L.; Dorsey, B. D.; Ator, M. A.; Ruggeri, B. A.; Cheng, M. Anaplastic lymphoma kinase activity is essential for the proliferation and survival of anaplastic large-cell lymphoma cells. Blood 2006, 107, 1617-1623.
-
(2006)
Blood
, vol.107
, pp. 1617-1623
-
-
Wan, W.1
Albom, M.S.2
Lu, L.3
Quail, M.R.4
Becknell, N.C.5
Weinberg, L.R.6
Reddy, D.R.7
Holskin, B.P.8
Angeles, T.S.9
Underiner, T.L.10
Meyer, S.L.11
Hudkins, R.L.12
Dorsey, B.D.13
Ator, M.A.14
Ruggeri, B.A.15
Cheng, M.16
-
35
-
-
32344432487
-
Design and synthesis of 5-aryl-pyridone-carboxamides as inhibitors of anaplastic lymphoma kinase
-
Li, R.; Xue, L.; Zhu, T.; Jiang, Q.; Cui, X.; Yan, Z.; McGee, D.; Wang, J.; Gantla, V. R.; Pickens, J. C.; McGrath, D.; Chucholowski, A.; Morris, S. W.; Webb, T. R. Design and synthesis of 5-aryl-pyridone-carboxamides as inhibitors of anaplastic lymphoma kinase. J. Med. Chem. 2006, 49, 1006-1015.
-
(2006)
J. Med. Chem.
, vol.49
, pp. 1006-1015
-
-
Li, R.1
Xue, L.2
Zhu, T.3
Jiang, Q.4
Cui, X.5
Yan, Z.6
McGee, D.7
Wang, J.8
Gantla, V.R.9
Pickens, J.C.10
McGrath, D.11
Chucholowski, A.12
Morris, S.W.13
Webb, T.R.14
-
36
-
-
27944485366
-
Inhibition of ALK enzymatic activity in T-cell lymphoma cells induces apoptosis and suppresses proliferation and STAT3 phosphorylation independently of Jak3
-
Marzec, M.; Kasprzycka, M.; Ptasznik, A.; Wlodarski, P.; Zhang, Q.; Odum, N.; Wasik, M. A. Inhibition of ALK enzymatic activity in T-cell lymphoma cells induces apoptosis and suppresses proliferation and STAT3 phosphorylation independently of Jak3. Lab. Invest 2005, 85, 1544-1554.
-
(2005)
Lab. Invest
, vol.85
, pp. 1544-1554
-
-
Marzec, M.1
Kasprzycka, M.2
Ptasznik, A.3
Wlodarski, P.4
Zhang, Q.5
Odum, N.6
Wasik, M.A.7
-
37
-
-
0035829463
-
Optimization of 4-phenylamino-3-quinolinecarbonitriles as potent inhibitors of Src kinase activity
-
Boschelli, D. H.; Ye, F.; Wang, Y. D.; Dutia, M.; Johnson, S. L.; Wu, B.; Miller, K.; Powell, D. W.; Yaczko, D.; Young, M.; Tischler, M.; Arndt, K.; Discafani, C.; Etienne, C.; Gibbons, J.; Grod, J.; Lucas, J.; Weber, J. M.; Boschelli, F. Optimization of 4-phenylamino-3-quinolinecarbonitriles as potent inhibitors of Src kinase activity. J. Med. Chem. 2001, 44, 3965-3977.
-
(2001)
J. Med. Chem.
, vol.44
, pp. 3965-3977
-
-
Boschelli, D.H.1
Ye, F.2
Wang, Y.D.3
Dutia, M.4
Johnson, S.L.5
Wu, B.6
Miller, K.7
Powell, D.W.8
Yaczko, D.9
Young, M.10
Tischler, M.11
Arndt, K.12
Discafani, C.13
Etienne, C.14
Gibbons, J.15
Grod, J.16
Lucas, J.17
Weber, J.M.18
Boschelli, F.19
-
38
-
-
0038035638
-
Sensitivity to imatinib but low frequency of the TEL/PDGFRbeta fusion protein in chronic myelomonocytic leukemia
-
Gunby, R. H.; Cazzaniga, G.; Tassi, E.; Le Coutre, P.; Pogliani, E.; Specchia, G.; Biondi, A.; Gambacorti-Passerini, C. Sensitivity to imatinib but low frequency of the TEL/PDGFRbeta fusion protein in chronic myelomonocytic leukemia. Haematologica 2003, 88, 408-415.
-
(2003)
Haematologica
, vol.88
, pp. 408-415
-
-
Gunby, R.H.1
Cazzaniga, G.2
Tassi, E.3
Le Coutre, P.4
Pogliani, E.5
Specchia, G.6
Biondi, A.7
Gambacorti-Passerini, C.8
-
39
-
-
6044271269
-
Swiss-Prot: Juggling between evolution and stability
-
Bairoch, A.; Boeckmann, B.; Ferro, S.; Gasteiger, E. Swiss-Prot: juggling between evolution and stability. Briefings Bioinf. 2004, 5, 39-55.
-
(2004)
Briefings Bioinf.
, vol.5
, pp. 39-55
-
-
Bairoch, A.1
Boeckmann, B.2
Ferro, S.3
Gasteiger, E.4
-
40
-
-
0030801002
-
Gapped BLAST and PSI-BLAST: A new generation of protein database search programs
-
Altschul, S. F.; Madden, T. L.; Schaffer, A. A.; Zhang, J.; Zhang, Z.; Miller, W.; Lipman, D. J. Gapped BLAST and PSI-BLAST: a new generation of protein database search programs. Nucleic Acids Res. 1997, 25, 3389-3402.
-
(1997)
Nucleic Acids Res.
, vol.25
, pp. 3389-3402
-
-
Altschul, S.F.1
Madden, T.L.2
Schaffer, A.A.3
Zhang, J.4
Zhang, Z.5
Miller, W.6
Lipman, D.J.7
-
41
-
-
19944426826
-
BODIL: A molecular modeling environment for structure-function analysis and drug design
-
Lehtonen, J. V.; Still, D. J.; Rantanen, V. V.; Ekholm, J.; Bjorklund, D.; Iftikhar, Z.; Huhtala, M.; Repo, S.; Jussila, A.; Jaakkola, J.; Pentikainen, O.; Nyronen, T.; Salminen, T.; Gyllenberg, M.; Johnson, M. S. BODIL: a molecular modeling environment for structure-function analysis and drug design. J. Comput.-Aided Mol. Des. 2004, 18, 401-419.
-
(2004)
J. Comput.-Aided Mol. Des.
, vol.18
, pp. 401-419
-
-
Lehtonen, J.V.1
Still, D.J.2
Rantanen, V.V.3
Ekholm, J.4
Bjorklund, D.5
Iftikhar, Z.6
Huhtala, M.7
Repo, S.8
Jussila, A.9
Jaakkola, J.10
Pentikainen, O.11
Nyronen, T.12
Salminen, T.13
Gyllenberg, M.14
Johnson, M.S.15
-
42
-
-
0000931192
-
Fast multiple alignment of ungapped DNA sequences using information theory and a relaxation method
-
Schneider, T. D.; Mastronarde, D. Fast multiple alignment of ungapped DNA sequences using information theory and a relaxation method. Discrete Applied Mathematics 1996, 71, 259-268.
-
(1996)
Discrete Applied Mathematics
, vol.71
, pp. 259-268
-
-
Schneider, T.D.1
Mastronarde, D.2
-
43
-
-
0027361123
-
A structural basis for sequence comparisons. An evaluation of scoring methodologies
-
Johnson, M. S.; Overington, J. P. A structural basis for sequence comparisons. An evaluation of scoring methodologies. J. Mol. Biol. 1993, 233, 716-738.
-
(1993)
J. Mol. Biol.
, vol.233
, pp. 716-738
-
-
Johnson, M.S.1
Overington, J.P.2
-
44
-
-
0033873929
-
Comparative protein structure modeling of genes and genomes
-
Marti-Renom, M. A.; Stuart, A. C.; Fiser, A.; Sanchez, R.; Melo, F.; Sali, A. Comparative protein structure modeling of genes and genomes. Annu. Rev. Biophys. Biomol. Struct. 2000, 29, 291-325.
-
(2000)
Annu. Rev. Biophys. Biomol. Struct.
, vol.29
, pp. 291-325
-
-
Marti-Renom, M.A.1
Stuart, A.C.2
Fiser, A.3
Sanchez, R.4
Melo, F.5
Sali, A.6
-
45
-
-
0000243829
-
PROCHECK: A program to check the stereochemical quality of protein structures
-
Laskowski, R. A.; MacArthur, M. W.; Moss, D. S.; Thornton, J. M. PROCHECK: a program to check the stereochemical quality of protein structures. J. Appl. Crystallogr. 1993, 26, 283-291.
-
(1993)
J. Appl. Crystallogr.
, vol.26
, pp. 283-291
-
-
Laskowski, R.A.1
MacArthur, M.W.2
Moss, D.S.3
Thornton, J.M.4
-
46
-
-
0033625531
-
TEXshade: Shading and labeling of multiple sequence alignments using LATEX2 epsilon
-
Beitz, E. TEXshade: shading and labeling of multiple sequence alignments using LATEX2 epsilon. Bioinformatics 2000, 16, 135-139.
-
(2000)
Bioinformatics
, vol.16
, pp. 135-139
-
-
Beitz, E.1
|