-
1
-
-
0035800507
-
Clinical resistance to STI-571 cancer therapy caused by BCR-ABL gene mutation or amplification
-
DOI 10.1126/science.1062538
-
Gorre ME, Mohammed M, Ellwood K, Hsu N, Paquette R, Rao PN, et al. Clinical resistance to STI-571 cancer therapy caused by BCR-ABL gene mutation or amplification. Science 2001;293:876-80. (Pubitemid 32743979)
-
(2001)
Science
, vol.293
, Issue.5531
, pp. 876-880
-
-
Gorre, M.E.1
Mohammed, M.2
Ellwood, K.3
Hsu, N.4
Paquette, R.5
Nagesh, R.P.6
Sawyers, C.L.7
-
2
-
-
45749084492
-
New Bcr-Abl inhibitors in chronic myeloid leukemia: Keeping resistance in check
-
DOI 10.1517/13543784.17.6.865
-
O'Hare T, Eide CA, Deininger MW. New Bcr-Abl inhibitors in chronic myeloid leukemia: keeping resistance in check. Expert Opin Investig Drugs 2008;17:865-78. (Pubitemid 351864324)
-
(2008)
Expert Opinion on Investigational Drugs
, vol.17
, Issue.6
, pp. 865-878
-
-
O'Hare, T.1
Eide, C.A.2
Deininger, M.W.3
-
3
-
-
34249018869
-
Gastrointestinal stromal tumour
-
DOI 10.1016/S0140-6736(07)60780-6, PII S0140673607607806
-
Rubin BP, Heinrich MC, Corless CL. Gastrointestinal stromal tumour. Lancet 2007;369:1731-41. (Pubitemid 46778870)
-
(2007)
Lancet
, vol.369
, Issue.9574
, pp. 1731-1741
-
-
Rubin, B.P.1
Heinrich, M.C.2
Corless, C.L.3
-
4
-
-
37049003546
-
Dynamics of BCR-ABL kinase domain mutations in chronic myeloid leukemia after sequential treatment with multiple tyrosine kinase inhibitors
-
DOI 10.1182/blood-2007-03-080838
-
Cortes J, Jabbour E, Kantarjian H, Yin CC, Shan J, O'Brien S, et al. Dynamics of BCR-ABL kinase domain mutations in chronic myeloid leukemia after sequential treatment with multiple tyrosine kinase inhibitors. Blood 2007;110:4005-11. (Pubitemid 350248456)
-
(2007)
Blood
, vol.110
, Issue.12
, pp. 4005-4011
-
-
Cortes, J.1
Jabbour, E.2
Kantarjian, H.3
Yin, C.C.4
Shan, J.5
O'Brien, S.6
Garcia-Manero, G.7
Giles, F.8
Breeden, M.9
Reeves, N.10
Wierda, W.G.11
Jones, D.12
-
5
-
-
44249125258
-
Challenges of detecting EGFR T790M in gefitinib/erlotinib-resistant tumours
-
DOI 10.1016/S0169-5002(08)70099-0, PII S0169500208700990
-
Janne PA. Challenges of detecting EGFR T790M in gefitinib/ erlotinibresistant tumours. Lung Cancer 2008;60 Suppl 2:S3-9. (Pubitemid 351726031)
-
(2008)
Lung Cancer
, vol.60
, Issue.SUPPL. 2
-
-
Janne, P.A.1
-
6
-
-
0037459344
-
Mechanisms of autoinhibition and STI-571/imatinib resistance revealed by mutagenesis of BCR-ABL
-
DOI 10.1016/S0092-8674(03)00190-9
-
Azam M, Latek RR, Daley GQ. Mechanisms of autoinhibition and STI-571/imatinib resistance revealed by mutagenesis of BCR-ABL. Cell 2003;112:831-43. (Pubitemid 36378885)
-
(2003)
Cell
, vol.112
, Issue.6
, pp. 831-843
-
-
Azam, M.1
Latek, R.R.2
Daley, G.Q.3
-
7
-
-
34247506325
-
Identification of BCR-ABL point mutations conferring resistance to the Abl kinase inhibitor AMN107 (nilotinib) by a random mutagenesis study
-
DOI 10.1182/blood-2006-01-015347
-
Ray A, Cowan-Jacob SW, Manley PW, Mestan J, Griffin JD. Identification of BCR-ABL point mutations conferring resistance to the Abl kinase inhibitor AMN107 (nilotinib) by a random mutagenesis study. Blood 2007;109:5011-5. (Pubitemid 46827801)
-
(2007)
Blood
, vol.109
, Issue.11
, pp. 5011-5015
-
-
Ray, A.1
Cowan-Jacob, S.W.2
Manley, P.W.3
Mestan, J.4
Griffin, J.D.5
-
8
-
-
73949083834
-
MEK1 mutations confer resistance to MEK and B-RAF inhibition
-
Emery CM, Vijayendran KG, Zipser MC, Sawyer AM, Niu L, Kim JJ, et al. MEK1 mutations confer resistance to MEK and B-RAF inhibition. Proc Natl Acad Sci U S A 2009;106:20411-6.
-
(2009)
Proc Natl Acad Sci U S A
, vol.106
, pp. 20411-20416
-
-
Emery, C.M.1
Vijayendran, K.G.2
Zipser, M.C.3
Sawyer, A.M.4
Niu, L.5
Kim, J.J.6
-
9
-
-
33749325184
-
Comparison of imatinib mesylate, dasatinib (BMS-354825), and nilotinib (AMN107) in an N-ethyl-N-nitrosourea (ENU)-based mutagenesis screen: High efficacy of drug combinations
-
DOI 10.1182/blood-2006-02-004580
-
Bradeen HA, Eide CA, O'Hare T, Johnson KJ, Willis SG, Lee FY, et al. Comparison of imatinib mesylate, dasatinib (BMS-354825), and nilotinib (AMN107) in an N-ethyl-N-nitrosourea (ENU)-based mutagenesis screen: high efficacy of drug combinations. Blood 2006;108:2332-8. (Pubitemid 44497517)
-
(2006)
Blood
, vol.108
, Issue.7
, pp. 2332-2338
-
-
Bradeen, H.A.1
Eide, C.A.2
O'Hare, T.3
Johnson, K.J.4
Willis, S.G.5
Lee, F.Y.6
Druker, B.J.7
Deininger, M.W.8
-
10
-
-
43749086323
-
T315I and preempts in vitro resistance when combined with nilotinib or dasatinib
-
DOI 10.1073/pnas.0800587105
-
O'Hare T, Eide CA, Tyner JW, Corbin AS, Wong MJ, Buchanan S, et al. SGX393 inhibits the CML mutant Bcr-AblT315I and preempts in vitro resistance when combined with nilotinib or dasatinib. Proc Natl Acad Sci U S A 2008;105:5507-12. (Pubitemid 351753893)
-
(2008)
Proceedings of the National Academy of Sciences of the United States of America
, vol.105
, Issue.14
, pp. 5507-5512
-
-
O'Hare, T.1
Eide, C.A.2
Tyner, J.W.3
Corbin, A.S.4
Wong, M.J.5
Buchanan, S.6
Holme, K.7
Jessen, K.A.8
Tang, C.9
Lewis, H.A.10
Romero, R.D.11
Burley, S.K.12
Deininger, M.W.13
-
11
-
-
33745069351
-
Bcr-Abl resistance screening predicts a limited spectrum of point mutations to be associated with clinical resistance to the Abl kinase inhibitor nilotinib (AMN107)
-
DOI 10.1182/blood-2005-12-010132
-
von Bubnoff N, Manley PW, Mestan J, Sanger J, Peschel C, Duyster J. Bcr-Abl resistance screening predicts a limited spectrum of point mutations to be associated with clinical resistance to the Abl kinase inhibitor nilotinib (AMN107). Blood 2006;108:1328-33. (Pubitemid 44232032)
-
(2006)
Blood
, vol.108
, Issue.4
, pp. 1328-1333
-
-
Von Bubnoff, N.1
Manley, P.W.2
Mestan, J.3
Sanger, J.4
Peschel, C.5
Duyster, J.6
-
12
-
-
44449151030
-
Drug development of MET inhibitors: Targeting oncogene addiction and expedience
-
DOI 10.1038/nrd2530, PII NRD2530
-
Comoglio PM, Giordano S, Trusolino L. Drug development of MET inhibitors: targeting oncogene addiction and expedience. Nat Rev Drug Discov 2008;7:504-16. (Pubitemid 351767118)
-
(2008)
Nature Reviews Drug Discovery
, vol.7
, Issue.6
, pp. 504-516
-
-
Comoglio, P.M.1
Giordano, S.2
Trusolino, L.3
-
13
-
-
73449111266
-
Developing c-MET pathway inhibitors for cancer therapy: Progress and challenges
-
Liu X, Newton RC, Scherle PA. Developing c-MET pathway inhibitors for cancer therapy: progress and challenges. Trends Mol Med 2009;16:37-45.
-
(2009)
Trends Mol Med
, vol.16
, pp. 37-45
-
-
Liu, X.1
Newton, R.C.2
Scherle, P.A.3
-
14
-
-
0141481285
-
A novel small molecule Met inhibitor induces apoptosis in cells transformed by the oncogenic TPR-MET tyrosine kinase
-
Sattler M, Pride YB, Ma P, Gramlich JL, Chu SC, Quinnan LA, et al. A novel small molecule met inhibitor induces apoptosis in cells transformed by the oncogenic TPR-MET tyrosine kinase. Cancer Res 2003;63:5462-9. (Pubitemid 37139865)
-
(2003)
Cancer Research
, vol.63
, Issue.17
, pp. 5462-5469
-
-
Sattler, M.1
Pride, Y.B.2
Ma, P.3
Gramlich, J.L.4
Chu, S.C.5
Quinnan, L.A.6
Shirazian, S.7
Liang, C.8
Podar, K.9
Christensen, J.G.10
Salgia, R.11
-
15
-
-
79960961887
-
Imidazo [1,2-b] pyridazine derivatives for the treatment of c-Met tyrosine kinase mediated disease
-
Furet P, McCarthy C, Schoepfer J, Spanka C, Stang M, Stauffer F inventors; Novartis AG (Lichtstrasse 35, Basel, CH-4056, CH), assignee. WO/2009/106577
-
Furet P, McCarthy C, Schoepfer J, Spanka C, Stang M, Stauffer F inventors; Novartis AG (Lichtstrasse 35, Basel, CH-4056, CH), assignee. Imidazo [1,2-b] pyridazine derivatives for the treatment of c-Met tyrosine kinase mediated disease. WO/2009/106577. 2009.
-
(2009)
-
-
-
16
-
-
46849101000
-
Discovery of a potent, selective, and orally bioavailable c-met inhibitor: 1-(2-hydroxy-2-methylpropyl)-N-(5-(7-methoxyquinolin-4-yloxy)pyridin- 2-yl) -5-methyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxamide (AMG 458)
-
DOI 10.1021/jm800401t
-
Liu L, Siegmund A, Xi N, Kaplan-Lefko P, Rex K, Chen A, et al. Discovery of a potent, selective, and orally bioavailable c-Met inhibitor: 1-(2-hydroxy-2-methylpropyl)-N-(5-(7-methoxyquinolin-4-yloxy)pyridin-2-yl) -5-methyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxamide (AMG 458). J Med Chem 2008;51:3688-91. (Pubitemid 351956499)
-
(2008)
Journal of Medicinal Chemistry
, vol.51
, Issue.13
, pp. 3688-3691
-
-
Liu, L.1
Siegmund, A.2
Xi, N.3
Kaplan-Lefko, P.4
Rex, K.5
Chen, A.6
Lin, J.7
Moriguchi, J.8
Berry, L.9
Huang, L.10
Teffera, Y.11
Yang, Y.12
Zhang, Y.13
Bellon, S.F.14
Lee, M.15
Shimanovich, R.16
Bak, A.17
Dominguez, C.18
Norman, M.H.19
Harmange, J.-C.20
Dussault, I.21
Kim, T.-S.22
more..
-
18
-
-
33644875355
-
Scaling and assessment of data quality
-
Evans P. Scaling and assessment of data quality. Acta Crystallogr D Biol Crystallogr 2006;62:72-82.
-
(2006)
Acta Crystallogr D Biol Crystallogr
, vol.62
, pp. 72-82
-
-
Evans, P.1
-
19
-
-
34447508216
-
Phaser crystallographic software
-
DOI 10.1107/S0021889807021206, PII S0021889807021206
-
McCoy AJ, Grosse-Kunstleve RW, Adams PD, Winn MD, Storoni LC, Read RJ. Phaser crystallographic software. J Appl Crystallogr 2007;40:658-74. (Pubitemid 47080256)
-
(2007)
Journal of Applied Crystallography
, vol.40
, Issue.4
, pp. 658-674
-
-
McCoy, A.J.1
Grosse-Kunstleve, R.W.2
Adams, P.D.3
Winn, M.D.4
Storoni, L.C.5
Read, R.J.6
-
20
-
-
76449098262
-
PHENIX: A comprehensive Python-based system for macro-molecular structure solution
-
Adams PD, Afonine PV, Bunkoczi G, Chen VB, Davis IW, Echols N, et al. PHENIX: a comprehensive Python-based system for macro-molecular structure solution. Acta Crystallogr D Biol Crystallogr 2010;66:213-21.
-
(2010)
Acta Crystallogr D Biol Crystallogr
, vol.66
, pp. 213-221
-
-
Adams, P.D.1
Afonine, P.V.2
Bunkoczi, G.3
Chen, V.B.4
Davis, I.W.5
Echols, N.6
-
21
-
-
77955445279
-
-
version 2.8.0. Cambridge, UK: Global Phasing Ltd
-
Bricogne G, Blanc E, Brandl M, Flensburg C, Keller P, Paciorek W, et al. BUSTER, version 2.8.0. Cambridge, UK: Global Phasing Ltd;2009.
-
(2009)
BUSTER
-
-
Bricogne, G.1
Blanc, E.2
Brandl, M.3
Flensburg, C.4
Keller, P.5
Paciorek, W.6
-
23
-
-
33947207989
-
Lung cancer cell lines harboring Met gene amplification are dependent on Met for growth and survival
-
DOI 10.1158/0008-5472.CAN-06-3495
-
Lutterbach B, Zeng Q, Davis LJ, Hatch H, Hang G, Kohl NE, et al. Lung cancer cell lines harboring MET gene amplification are dependent on Met for growth and survival. Cancer Res 2007;67:2081-8. (Pubitemid 46424226)
-
(2007)
Cancer Research
, vol.67
, Issue.5
, pp. 2081-2088
-
-
Lutterbach, B.1
Zeng, Q.2
Davis, L.J.3
Hatch, H.4
Hang, G.5
Kohl, N.E.6
Gibbs, J.B.7
Pan, B.-S.8
-
24
-
-
33144462553
-
Amplification of MET may identify a subset of cancers with extreme sensitivity to the selective tyrosine kinase inhibitor PHA-665752
-
DOI 10.1073/pnas.0508776103
-
Smolen GA, Sordella R, Muir B, Mohapatra G, Barmettler A, Archibald H, et al. Amplification of MET may identify a subset of cancers with extreme sensitivity to the selective tyrosine kinase inhibitor PHA-665752. Proc Natl Acad Sci U S A 2006;103:2316-21. (Pubitemid 43271667)
-
(2006)
Proceedings of the National Academy of Sciences of the United States of America
, vol.103
, Issue.7
, pp. 2316-2321
-
-
Smolen, G.A.1
Sordella, R.2
Muir, B.3
Mohapatra, G.4
Barmettler, A.5
Archibald, H.6
Kim, W.J.7
Okimoto, R.A.8
Bell, D.W.9
Sgroi, D.C.10
Christensen, J.G.11
Settleman, J.12
Haber, D.A.13
-
25
-
-
51849105600
-
Discovery of pyrrolopyridine-pyridone based inhibitors of Met kinase: Synthesis, X-ray crystallographic analysis, and biological activities
-
Kim KS, Zhang L, Schmidt R, Cai ZW, Wei D, Williams DK, et al. Discovery of pyrrolopyridine-pyridone based inhibitors of Met kinase: synthesis, X-ray crystallographic analysis, and biological activities. J Med Chem 2008;51:5330-41.
-
(2008)
J Med Chem
, vol.51
, pp. 5330-5341
-
-
Kim, K.S.1
Zhang, L.2
Schmidt, R.3
Cai, Z.W.4
Wei, D.5
Williams, D.K.6
-
26
-
-
67049134253
-
Enzymatic characterization of c-Met receptor tyrosine kinase oncogenic mutants and kinetic studies with aminopyridine and triazolopyrazine inhibitors
-
Timofeevski SL, McTigue MA, Ryan K, Cui J, Zou HY, Zhu JX, et al. Enzymatic characterization of c-Met receptor tyrosine kinase oncogenic mutants and kinetic studies with aminopyridine and triazolopyrazine inhibitors. Biochemistry 2009;48:5339-49.
-
(2009)
Biochemistry
, vol.48
, pp. 5339-5349
-
-
Timofeevski, S.L.1
McTigue, M.A.2
Ryan, K.3
Cui, J.4
Zou, H.Y.5
Zhu, J.X.6
-
27
-
-
70350230210
-
Inhibition of tumor cell growth, invasion, and metastasis by EXEL-2880 (XL880, GSK1363089), a novel inhibitor of HGF and VEGF receptor tyrosine kinases
-
Qian F, Engst S, Yamaguchi K, Yu P, Won KA, Mock L, et al. Inhibition of tumor cell growth, invasion, and metastasis by EXEL-2880 (XL880, GSK1363089), a novel inhibitor of HGF and VEGF receptor tyrosine kinases. Cancer Res 2009;69:8009-16.
-
(2009)
Cancer Res
, vol.69
, pp. 8009-8016
-
-
Qian, F.1
Engst, S.2
Yamaguchi, K.3
Yu, P.4
Won, K.A.5
Mock, L.6
-
28
-
-
17344381429
-
Germline and somatic mutations in the tyrosine kinase domain of the MET proto-oncogene in papillary renal carcinomas
-
Schmidt L, Duh FM, Chen F, Kishida T, Glenn G, Choyke P, et al. Germline and somatic mutations in the tyrosine kinase domain of the MET proto-oncogene in papillary renal carcinomas. Nat Genet 1997;16:68-73. (Pubitemid 27198158)
-
(1997)
Nature Genetics
, vol.16
, Issue.1
, pp. 68-73
-
-
Schmidt, L.1
Duh, F.-M.2
Chen, F.3
Kishida, T.4
Glenn, G.5
Choyke, P.6
Scherer, S.W.7
Zhuang, Z.8
Lubensky, I.9
Dean, M.10
Allikmets, R.11
Chidambaram, A.12
Bergerheim, U.R.13
Feltis, J.T.14
Casadevall, C.15
Zamarron, A.16
Bernues, M.17
Richard, S.18
Lips, C.J.M.19
-
29
-
-
0033535530
-
Novel mutations of the MET proto-oncogene in papillary renal carcinomas
-
Schmidt L, Junker K, Nakaigawa N, Kinjerski T, Weirich G, Miller M, et al. Novel mutations of the MET proto-oncogene in papillary renal carcinomas. Oncogene 1999;18:2343-50. (Pubitemid 29192711)
-
(1999)
Oncogene
, vol.18
, Issue.14
, pp. 2343-2350
-
-
Schmidt, L.1
Junker, K.2
Nakaigawa, N.3
Kinjerski, T.4
Weirich, G.5
Miller, M.6
Lubensky, I.7
Neumann, H.P.8
Brauch, H.9
Decker, J.10
Vocke, C.11
Brown, J.A.12
Jenkins, R.13
Richard, S.14
Bergerheim, U.15
Gerrard, B.16
Dean, M.17
Linehan, W.M.18
Zbar, B.19
-
30
-
-
0034673699
-
Somatic mutations of the MET oncogene are selected during metastatic spread of human HNSC carcinomas
-
Di Renzo MF, Olivero M, Martone T, Maffe A, Maggiora P, Stefani AD, et al. Somatic mutations of the MET oncogene are selected during metastatic spread of human HNSC carcinomas. Oncogene 2000;19:1547-55. (Pubitemid 30175676)
-
(2000)
Oncogene
, vol.19
, Issue.12
, pp. 1547-1555
-
-
Di, R.M.F.1
Olivero, M.2
Martone, T.3
Maffe, A.4
Maggiora, P.5
De Stefani, A.6
Valente, G.7
Giordano, S.8
Cortesina, G.9
Comoglio, P.M.10
-
31
-
-
0036896226
-
Novel somatic mutations of the MET oncogene in human carcinoma metastases activating cell motility and invasion
-
Lorenzato A, Olivero M, Patane S, Rosso E, Oliaro A, Comoglio PM, et al. Novel somatic mutations of the MET oncogene in human carcinoma metastases activating cell motility and invasion. Cancer Res 2002;62:7025-30. (Pubitemid 35424097)
-
(2002)
Cancer Research
, vol.62
, Issue.23
, pp. 7025-7030
-
-
Lorenzato, A.1
Olivero, M.2
Patane, S.3
Rosso, E.4
Oliaro, A.5
Comoglio, P.M.6
Di, R.M.F.7
-
32
-
-
33644872197
-
Structural characterization of autoinhibited c-Met kinase produced by coexpression in bacteria with phosphatase
-
DOI 10.1073/pnas.0600048103
-
Wang W, Marimuthu A, Tsai J, Kumar A, Krupka HI, Zhang C, et al. Structural characterization of autoinhibited c-Met kinase produced by coexpression in bacteria with phosphatase. Proc Natl Acad Sci U S A 2006;103:3563-8. (Pubitemid 43376595)
-
(2006)
Proceedings of the National Academy of Sciences of the United States of America
, vol.103
, Issue.10
, pp. 3563-3568
-
-
Wang, W.1
Marimuthu, A.2
Tsai, J.3
Kumar, A.4
Krupka, H.I.5
Zhang, C.6
Powell, B.7
Suzuki, Y.8
Nguyen, H.9
Tabrizizad, M.10
Luu, C.11
West, B.L.12
-
33
-
-
71049184440
-
Discovery and optimization of potent and selective triazolopyridazine series of c-Met inhibitors
-
Boezio AA, Berry L, Albrecht BK, Bauer D, Bellon SF, Bode C, et al. Discovery and optimization of potent and selective triazolopyridazine series of c-Met inhibitors. Bioorg Med Chem Lett 2009;19:6307-12.
-
(2009)
Bioorg Med Chem Lett
, vol.19
, pp. 6307-6312
-
-
Boezio, A.A.1
Berry, L.2
Albrecht, B.K.3
Bauer, D.4
Bellon, S.F.5
Bode, C.6
-
34
-
-
73149091443
-
SGX523 is an exquisitely selective, ATP-competitive inhibitor of the MET receptor tyrosine kinase with antitumor activity in vivo
-
Buchanan SG, Hendle J, Lee PS, Smith CR, Bounaud PY, Jessen KA, et al. SGX523 is an exquisitely selective, ATP-competitive inhibitor of the MET receptor tyrosine kinase with antitumor activity in vivo. Mol Cancer Ther 2009;8:3181-90.
-
(2009)
Mol Cancer Ther
, vol.8
, pp. 3181-3190
-
-
Buchanan, S.G.1
Hendle, J.2
Lee, P.S.3
Smith, C.R.4
Bounaud, P.Y.5
Jessen, K.A.6
-
35
-
-
79960958002
-
JNJ-38877605: A selective oral c-Met inhibitor for the treatment of cancer
-
[abstract]. Exhibit Hall A-C, Poster Section 26. Washington (DC): AACR; Abstract nr 3628
-
King P. JNJ-38877605: a selective oral c-Met inhibitor for the treatment of cancer [abstract]. In: Proceedings of the 101st Annual Meeting of the American Association for Cancer Research; 2010 Apr 20; Exhibit Hall A-C, Poster Section 26. Washington (DC): AACR; 2010. Abstract nr 3628.
-
(2010)
Proceedings of the 101st Annual Meeting of the American Association for Cancer Research; 2010 Apr 20
-
-
King, P.1
-
36
-
-
76149091189
-
Small molecule c-Met kinase inhibitors: A review of recent patents
-
Porter J. Small molecule c-Met kinase inhibitors: a review of recent patents. Expert Opin Ther Pat 2010;20:159-77.
-
(2010)
Expert Opin Ther Pat
, vol.20
, pp. 159-177
-
-
Porter, J.1
-
37
-
-
43949142094
-
Discovery and optimization of triazolopyridazines as potent and selective inhibitors of the c-Met kinase
-
DOI 10.1021/jm800043g
-
Albrecht BK, Harmange JC, Bauer D, Berry L, Bode C, Boezio AA, et al. Discovery and optimization of triazolopyridazines as potent and selective inhibitors of the c-Met kinase. J Med Chem 2008;51:2879-82. (Pubitemid 351706015)
-
(2008)
Journal of Medicinal Chemistry
, vol.51
, Issue.10
, pp. 2879-2882
-
-
Albrecht, B.K.1
Harmange, J.-C.2
Bauer, D.3
Berry, L.4
Bode, C.5
Boezio, A.A.6
Chen, A.7
Choquette, D.8
Dussault, I.9
Fridrich, C.10
Hirai, S.11
Hoffman, D.12
Larrow, J.F.13
Kaplan-Lefko, P.14
Lin, J.15
Lohman, J.16
Long, A.M.17
Moriguchi, J.18
O'Connor, A.19
Potashman, M.H.20
Reese, M.21
Rex, K.22
Siegmund, A.23
Shah, K.24
Shimanovich, R.25
Springer, S.K.26
Teffera, Y.27
Yang, Y.28
Zhang, Y.29
Bellon, S.F.30
more..
-
38
-
-
41449107739
-
c-Met inhibitors with novel binding mode show activity against several hereditary papillary renal cell carcinoma-related mutations
-
Bellon SF, Kaplan-Lefko P, Yang Y, Zhang Y, Moriguchi J, Rex K, et al. c-Met inhibitors with novel binding mode show activity against several hereditary papillary renal cell carcinoma-related mutations. J Biol Chem 2008;283:2675-83.
-
(2008)
J Biol Chem
, vol.283
, pp. 2675-2683
-
-
Bellon, S.F.1
Kaplan-Lefko, P.2
Yang, Y.3
Zhang, Y.4
Moriguchi, J.5
Rex, K.6
-
39
-
-
33749435816
-
Allelic dilution obscures detection of a biologically significant resistance mutation in EGFR-amplified lung cancer
-
DOI 10.1172/JCI28656
-
Engelman JA, Mukohara T, Zejnullahu K, Lifshits E, Borras AM, Gale CM, et al. Allelic dilution obscures detection of a biologically significant resistance mutation in EGFR-amplified lung cancer. J Clin Invest 2006;116:2695-706. (Pubitemid 44511633)
-
(2006)
Journal of Clinical Investigation
, vol.116
, Issue.10
, pp. 2695-2706
-
-
Engelman, J.A.1
Mukohara, T.2
Zejnullahu, K.3
Lifshits, E.4
Borras, A.M.5
Gale, C.-M.6
Naumov, G.N.7
Yeap, B.Y.8
Jarrell, E.9
Sun, J.10
Tracy, S.11
Zhao, X.12
Heymach, J.V.13
Johnson, B.E.14
Cantley, L.C.15
Janne, P.A.16
-
40
-
-
79551559942
-
Multiple mutations and bypass mechanisms can contribute to development of acquired resistance to MET inhibitors
-
Qi J, McTigue MA, Rogers A, Lifshits E, Christensen JG, Janne PA, et al. Multiple mutations and bypass mechanisms can contribute to development of acquired resistance to MET inhibitors. Cancer Res 2011;71:1081-91.
-
(2011)
Cancer Res
, vol.71
, pp. 1081-1091
-
-
Qi, J.1
McTigue, M.A.2
Rogers, A.3
Lifshits, E.4
Christensen, J.G.5
Janne, P.A.6
-
41
-
-
56249137901
-
HER kinase activation confers resistance to MET tyrosine kinase inhibition in MET oncogene-addicted gastric cancer cells
-
Bachleitner-Hofmann T, Sun MY, Chen CT, Tang L, Song L, Zeng Z, et al. HER kinase activation confers resistance to MET tyrosine kinase inhibition in MET oncogene-addicted gastric cancer cells. Mol Cancer Ther 2008;7:3499-508.
-
(2008)
Mol Cancer Ther
, vol.7
, pp. 3499-3508
-
-
Bachleitner-Hofmann, T.1
Sun, M.Y.2
Chen, C.T.3
Tang, L.4
Song, L.5
Zeng, Z.6
-
42
-
-
76749157917
-
Acquired resistance of non-small cell lung cancer cells to MET kinase inhibition is mediated by a switch to epidermal growth factor receptor dependency
-
McDermott U, Pusapati RV, Christensen JG, Gray NS, Settleman J. Acquired resistance of non-small cell lung cancer cells to MET kinase inhibition is mediated by a switch to epidermal growth factor receptor dependency. Cancer Res 2010;70:1625-34.
-
(2010)
Cancer Res
, vol.70
, pp. 1625-1634
-
-
McDermott, U.1
Pusapati, R.V.2
Christensen, J.G.3
Gray, N.S.4
Settleman, J.5
-
43
-
-
77957328515
-
MET and KRAS gene amplification mediates acquired resistance to MET tyrosine kinase inhibitors
-
Cepero V, Sierra JR, Corso S, Ghiso E, Casorzo L, Perera T, et al. MET and KRAS gene amplification mediates acquired resistance to MET tyrosine kinase inhibitors. Cancer Res 2010;70:7580-90.
-
(2010)
Cancer Res
, vol.70
, pp. 7580-7590
-
-
Cepero, V.1
Sierra, J.R.2
Corso, S.3
Ghiso, E.4
Casorzo, L.5
Perera, T.6
-
44
-
-
77952612183
-
Activation of HER family members in gastric carcinoma cells mediates resistance to MET inhibition
-
Corso S, Ghiso E, Cepero V, Sierra JR, Migliore C, Bertotti A, et al. Activation of HER family members in gastric carcinoma cells mediates resistance to MET inhibition. Mol Cancer 2010;9:121.
-
(2010)
Mol Cancer
, vol.9
, pp. 121
-
-
Corso, S.1
Ghiso, E.2
Cepero, V.3
Sierra, J.R.4
Migliore, C.5
Bertotti, A.6
-
45
-
-
34249075147
-
MET amplification leads to gefitinib resistance in lung cancer by activating ERBB3 signaling
-
DOI 10.1126/science.1141478
-
Engelman JA, Zejnullahu K, Mitsudomi T, Song Y, Hyland C, Park JO, et al. MET amplification leads to gefitinib resistance in lung cancer by activating ERBB3 signaling. Science 2007;316:1039-43. (Pubitemid 46799492)
-
(2007)
Science
, vol.316
, Issue.5827
, pp. 1039-1043
-
-
Engelman, J.A.1
Zejnullahu, K.2
Mitsudomi, T.3
Song, Y.4
Hyland, C.5
Joon, O.P.6
Lindeman, N.7
Gale, C.-M.8
Zhao, X.9
Christensen, J.10
Kosaka, T.11
Holmes, A.J.12
Rogers, A.M.13
Cappuzzo, F.14
Mok, T.15
Lee, C.16
Johnson, B.E.17
Cantley, L.C.18
Janne, P.A.19
-
46
-
-
73649102105
-
Preexistence and clonal selection of MET amplification in EGFR mutant NSCLC
-
Turke AB, Zejnullahu K, Wu YL, Song Y, Dias-Santagata D, Lifshits E, et al. Preexistence and clonal selection of MET amplification in EGFR mutant NSCLC. Cancer Cell 2010;17:77-88.
-
(2010)
Cancer Cell
, vol.17
, pp. 77-88
-
-
Turke, A.B.1
Zejnullahu, K.2
Wu, Y.L.3
Song, Y.4
Dias-Santagata, D.5
Lifshits, E.6
-
47
-
-
56449089812
-
Hepatocyte growth factor induces gefitinib resistance of lung adenocarcinoma with epidermal growth factor receptor-activating mutations
-
Yano S, Wang W, Li Q, Matsumoto K, Sakurama H, Nakamura T, et al. Hepatocyte growth factor induces gefitinib resistance of lung adenocarcinoma with epidermal growth factor receptor-activating mutations. Cancer Res 2008;68:9479-87.
-
(2008)
Cancer Res
, vol.68
, pp. 9479-9487
-
-
Yano, S.1
Wang, W.2
Li, Q.3
Matsumoto, K.4
Sakurama, H.5
Nakamura, T.6
|