-
1
-
-
49749110720
-
Gene expansion and retention leads to a diverse tyrosine kinase superfamily in amphioxus
-
D'Aniello S, Irimia M, Maeso I, et al. Gene expansion and retention leads to a diverse tyrosine kinase superfamily in amphioxus. Mol Biol Evol 2008;25:1841-54.
-
(2008)
Mol Biol Evol
, vol.25
, pp. 1841-1854
-
-
D'Aniello, S.1
Irimia, M.2
Maeso, I.3
-
2
-
-
0345601083
-
Met, metastasis, motility and more
-
Birchmeier C, Birchmeier W, Gherardi E, Vande Woude GF. Met, metastasis, motility and more. Nat Rev Mol Cell Biol 2003;4:915-25.
-
(2003)
Nat Rev Mol Cell Biol
, vol.4
, pp. 915-925
-
-
Birchmeier, C.1
Birchmeier, W.2
Gherardi, E.3
Vande Woude, G.F.4
-
4
-
-
0038724909
-
c-Met: Structure, functions and potential for therapeutic inhibition
-
Ma PC, Maulik G, Christensen J, Salgia R. c-Met: structure, functions and potential for therapeutic inhibition. CancerMetastasis Rev 2003;22:309-25.
-
(2003)
CancerMetastasis Rev
, vol.22
, pp. 309-325
-
-
Ma, P.C.1
Maulik, G.2
Christensen, J.3
Salgia, R.4
-
5
-
-
44449151030
-
Drug development of MET inhibitors: Targeting oncogene addiction and expedience
-
Comoglio PM, Giordano S, Trusolino L. Drug development of MET inhibitors: targeting oncogene addiction and expedience. Nat Rev Drug Discov 2008;7:504-16.
-
(2008)
Nat Rev Drug Discov
, vol.7
, pp. 504-516
-
-
Comoglio, P.M.1
Giordano, S.2
Trusolino, L.3
-
6
-
-
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, 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.
-
(1997)
Nat Genet
, vol.16
, pp. 68-73
-
-
Schmidt, L.1
Duh, F.M.2
Chen, F.3
-
7
-
-
34249075147
-
METamplification leads to gefitinib resistance in lung cancer by activating ERBB3 signaling
-
Engelman JA, Zejnullahu K, Mitsudomi T, et al. METamplification leads to gefitinib resistance in lung cancer by activating ERBB3 signaling. Science (New York) 2007;316:1039-43.
-
(2007)
Science (New York)
, vol.316
, pp. 1039-1043
-
-
Engelman, J.A.1
Zejnullahu, K.2
Mitsudomi, T.3
-
8
-
-
0030690583
-
Met and hepatocyte growth factor/scatter factor expression in human gliomas
-
Koochekpour S, Jeffers M, Rulong S, et al.Met and hepatocyte growth factor/scatter factor expression in human gliomas. Cancer Res 1997;57:5391-8.
-
(1997)
Cancer Res
, vol.57
, pp. 5391-5398
-
-
Koochekpour, S.1
Jeffers, M.2
Rulong, S.3
-
9
-
-
0036365052
-
In vivo targeting of SF/HGF and cmet expression via U1snRNA/ribozymes inhibits glioma growth and angiogenesis and promotes apoptosis
-
Abounader R, Lal B, Luddy C, et al. In vivo targeting of SF/HGF and cmet expression via U1snRNA/ribozymes inhibits glioma growth and angiogenesis and promotes apoptosis. FASEB J 2002;16:108-10.
-
(2002)
FASEB J
, vol.16
, pp. 108-110
-
-
Abounader, R.1
Lal, B.2
Luddy, C.3
-
10
-
-
32944467848
-
Fully human monoclonal antibodies to hepatocyte growth factor with therapeutic potential against hepatocyte growth factor/c-Met-dependent human tumors
-
Burgess T, Coxon A, Meyer S, et al. Fully human monoclonal antibodies to hepatocyte growth factor with therapeutic potential against hepatocyte growth factor/c-Met-dependent human tumors. Cancer Res 2006; 66:1721-9.
-
(2006)
Cancer Res
, vol.66
, pp. 1721-1729
-
-
Burgess, T.1
Coxon, A.2
Meyer, S.3
-
11
-
-
0035912757
-
Neutralizing monoclonal antibodies to hepatocyte growth factor/scatter factor (HGF/SF) display antitumor activity in animal models
-
Cao B, Su Y, Oskarsson M, et al. Neutralizing monoclonal antibodies to hepatocyte growth factor/scatter factor (HGF/SF) display antitumor activity in animal models. Proc Natl Acad Sci U S A 2001;98:7443-8.
-
(2001)
Proc Natl Acad Sci U S A
, vol.98
, pp. 7443-7448
-
-
Cao, B.1
Su, Y.2
Oskarsson, M.3
-
12
-
-
33750683969
-
A novel one-armed anti-c-Met antibody inhibits glioblastoma growth in vivo
-
Martens T, Schmidt NO, Eckerich C, et al. A novel one-armed anti-c-Met antibody inhibits glioblastoma growth in vivo. Clin Cancer Res 2006; 12:6144-52.
-
(2006)
Clin Cancer Res
, vol.12
, pp. 6144-6152
-
-
Martens, T.1
Schmidt, N.O.2
Eckerich, C.3
-
13
-
-
10744228765
-
A selective small molecule inhibitor of c-Met kinase inhibits c-Met-dependent phenotypes in vitro and exhibits cytoreductive antitumor activity in vivo
-
Christensen JG, Schreck R, Burrows J, et al. A selective small molecule inhibitor of c-Met kinase inhibits c-Met-dependent phenotypes in vitro and exhibits cytoreductive antitumor activity in vivo. Cancer Res 2003; 63:7345-55.
-
(2003)
Cancer Res
, vol.63
, pp. 7345-7355
-
-
Christensen, J.G.1
Schreck, R.2
Burrows, J.3
-
14
-
-
34249324494
-
-
Zou HY, Li Q, Lee JH, et al. An orally available small-molecule inhibitor of c-Met, PF-2341066, exhibits cytoreductive antitumor efficacy through antiproliferative and antiangiogenic mechanisms.Cancer Res 2007;67:4408-17.
-
Zou HY, Li Q, Lee JH, et al. An orally available small-molecule inhibitor of c-Met, PF-2341066, exhibits cytoreductive antitumor efficacy through antiproliferative and antiangiogenic mechanisms.Cancer Res 2007;67:4408-17.
-
-
-
-
15
-
-
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, 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
-
16
-
-
73149101361
-
A phase I study of a novel spectrum selective kinase inhibitor (SSKI), XL880, administered orally in patients with solid tumors
-
Philadelphia, PA;
-
LoRusso P, Appleman L, Heath E, et al. A phase I study of a novel spectrum selective kinase inhibitor (SSKI), XL880, administered orally in patients with solid tumors. AACR-NCI-EORTC; 2005 Nov 14-18; Pennsylvania Convention Center, Philadelphia, PA; 2005.
-
(2005)
AACR-NCI-EORTC; 2005 Nov 14-18; Pennsylvania Convention Center
-
-
LoRusso, P.1
Appleman, L.2
Heath, E.3
-
17
-
-
0029020282
-
Protein kinases 6. The eukaryotic protein kinase superfamily: Kinase (catalytic) domain structure and classification
-
Hanks SK, Hunter T. Protein kinases 6. The eukaryotic protein kinase superfamily: kinase (catalytic) domain structure and classification. FASEB J 1995;9:576-96.
-
(1995)
FASEB J
, vol.9
, pp. 576-596
-
-
Hanks, S.K.1
Hunter, T.2
-
18
-
-
38049018155
-
A quantitative analysis of kinase inhibitor selectivity
-
Karaman MW, Herrgard S, Treiber DK, et al. A quantitative analysis of kinase inhibitor selectivity. Nat Biotechnol 2008;26:127-32.
-
(2008)
Nat Biotechnol
, vol.26
, pp. 127-132
-
-
Karaman, M.W.1
Herrgard, S.2
Treiber, D.K.3
-
19
-
-
36549040859
-
The selectivity of protein kinase inhibitors: A further update
-
Bain J, Plater L, Elliott M, et al. The selectivity of protein kinase inhibitors: a further update. Biochem J 2007;408:297-315.
-
(2007)
Biochem J
, vol.408
, pp. 297-315
-
-
Bain, J.1
Plater, L.2
Elliott, M.3
-
20
-
-
0242268455
-
Crystal structure of the tyrosine kinase domain of the hepatocyte growth factor receptor c-Met and its complex with the microbial alkaloid K-252a
-
Schiering N, Knapp S, Marconi M, et al. Crystal structure of the tyrosine kinase domain of the hepatocyte growth factor receptor c-Met and its complex with the microbial alkaloid K-252a. Proc Natl Acad Sci U S A 2003;100:12654-9.
-
(2003)
Proc Natl Acad Sci U S A
, vol.100
, pp. 12654-12659
-
-
Schiering, N.1
Knapp, S.2
Marconi, M.3
-
21
-
-
0028103275
-
The CCP4 suite: Programs for protein crystallography
-
Collaborative Computational Project Number 4
-
Collaborative Computational Project Number 4. The CCP4 suite: programs for protein crystallography. Acta Crystallogr D Biol Crystallogr 1994;50:760-3.
-
(1994)
Acta Crystallogr D Biol Crystallogr
, vol.50
, pp. 760-763
-
-
-
22
-
-
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, 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.
-
(2003)
Cancer Res
, vol.63
, pp. 5462-5469
-
-
Sattler, M.1
Pride, Y.B.2
Ma, P.3
-
23
-
-
33745298429
-
Rational design of inhibitors that bind to inactive kinase conformations
-
Liu Y, Gray NS. Rational design of inhibitors that bind to inactive kinase conformations. Nat Chem Biol 2006;2:358-64.
-
(2006)
Nat Chem Biol
, vol.2
, pp. 358-364
-
-
Liu, Y.1
Gray, N.S.2
-
24
-
-
0037032835
-
The protein kinase complement of the human genome
-
Manning G, Whyte DB, Martinez R, Hunter T, Sudarsanam S. The protein kinase complement of the human genome. Science (New York) 2002;298:1912-34.
-
(2002)
Science (New York)
, vol.298
, pp. 1912-1934
-
-
Manning, G.1
Whyte, D.B.2
Martinez, R.3
Hunter, T.4
Sudarsanam, S.5
-
25
-
-
39749162787
-
Classifying protein kinase structures guides use of ligand-selectivity profiles to predict inactive conformations: Structure of lck/imatinib complex
-
Jacobs MD, Caron PR, Hare BJ. Classifying protein kinase structures guides use of ligand-selectivity profiles to predict inactive conformations: structure of lck/imatinib complex. Proteins 2008;70:1451-60.
-
(2008)
Proteins
, vol.70
, pp. 1451-1460
-
-
Jacobs, M.D.1
Caron, P.R.2
Hare, B.J.3
-
26
-
-
0022472582
-
Mechanism of met oncogene activation
-
Park M, Dean M, Cooper CS, et al. Mechanism of met oncogene activation. Cell 1986;45:895-904.
-
(1986)
Cell
, vol.45
, pp. 895-904
-
-
Park, M.1
Dean, M.2
Cooper, C.S.3
-
27
-
-
16844374901
-
A selective small molecule c-MET Inhibitor, PHA665752, cooperates with rapamycin
-
Ma PC, Schaefer E, Christensen JG, Salgia R. A selective small molecule c-MET Inhibitor, PHA665752, cooperates with rapamycin. Clin Cancer Res 2005;11:2312-9.
-
(2005)
Clin Cancer Res
, vol.11
, pp. 2312-2319
-
-
Ma, P.C.1
Schaefer, E.2
Christensen, J.G.3
Salgia, R.4
-
28
-
-
0033535530
-
Novel mutations of the MET proto-oncogene in papillary renal carcinomas
-
Schmidt L, Junker K, Nakaigawa N, et al. Novel mutations of the MET proto-oncogene in papillary renal carcinomas. Oncogene 1999;18:2343-50.
-
(1999)
Oncogene
, vol.18
, pp. 2343-2350
-
-
Schmidt, L.1
Junker, K.2
Nakaigawa, N.3
-
29
-
-
0030799090
-
Activating mutations for the met tyrosine kinase receptor in human cancer
-
Jeffers M, Schmidt L, Nakaigawa N, et al. Activating mutations for the met tyrosine kinase receptor in human cancer. Proc Natl Acad Sci U S A 1997;94:11445-50.
-
(1997)
Proc Natl Acad Sci U S A
, vol.94
, pp. 11445-11450
-
-
Jeffers, M.1
Schmidt, L.2
Nakaigawa, N.3
-
30
-
-
0034673699
-
Somatic mutations of the METoncogene are selected during metastatic spread of human HNSC carcinomas
-
Di Renzo MF, Olivero M, Martone T, et al. Somatic mutations of the METoncogene are selected during metastatic spread of human HNSC carcinomas. Oncogene 2000;19:1547-55.
-
(2000)
Oncogene
, vol.19
, pp. 1547-1555
-
-
Di Renzo, M.F.1
Olivero, M.2
Martone, T.3
-
31
-
-
33947207989
-
Lung cancer cell lines harboring MET gene amplification are dependent on Met for growth and survival
-
Lutterbach B, Zeng Q, Davis LJ, et al. Lung cancer cell lines harboring MET gene amplification are dependent on Met for growth and survival. Cancer Res 2007;67:2081-8.
-
(2007)
Cancer Res
, vol.67
, pp. 2081-2088
-
-
Lutterbach, B.1
Zeng, Q.2
Davis, L.J.3
-
32
-
-
33144462553
-
Amplification ofMETmay identify a subset of cancers with extreme sensitivity to the selective tyrosine kinase inhibitor PHA-665752
-
Smolen GA, Sordella R,Muir B, et al. Amplification ofMETmay 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.
-
(2006)
Proc Natl Acad Sci U S A
, vol.103
, pp. 2316-2321
-
-
Smolen, G.A.1
Sordella, R.2
Muir, B.3
-
33
-
-
0023661693
-
Scatter factor is a fibroblastderived modulator of epithelial cell mobility
-
Stoker M, Gherardi E, Perryman M, Gray J. Scatter factor is a fibroblastderived modulator of epithelial cell mobility. Nature 1987;327:239-42.
-
(1987)
Nature
, vol.327
, pp. 239-242
-
-
Stoker, M.1
Gherardi, E.2
Perryman, M.3
Gray, J.4
-
34
-
-
34248575532
-
A selective small molecule inhibitor of c-Met, PHA665752, inhibits tumorigenicity and angiogenesis in mouse lung cancer xenografts
-
Puri N, Khramtsov A, Ahmed S, et al. A selective small molecule inhibitor of c-Met, PHA665752, inhibits tumorigenicity and angiogenesis in mouse lung cancer xenografts. Cancer Res 2007;67:3529-34.
-
(2007)
Cancer Res
, vol.67
, pp. 3529-3534
-
-
Puri, N.1
Khramtsov, A.2
Ahmed, S.3
-
35
-
-
43949142094
-
Discovery and optimization of triazolopyridazines as potent and selective inhibitors of the c-Met kinase
-
Albrecht BK, Harmange JC, Bauer D, et al. Discovery and optimization of triazolopyridazines as potent and selective inhibitors of the c-Met kinase. J Med Chem 2008;51:2879-82.
-
(2008)
J Med Chem
, vol.51
, pp. 2879-2882
-
-
Albrecht, B.K.1
Harmange, J.C.2
Bauer, D.3
|