-
1
-
-
0035902180
-
Oncogenic kinase signalling
-
Blume-Jensen, P.; Hunter, T. Oncogenic kinase signalling. Nature 2001, 411, 355-365.
-
(2001)
Nature
, vol.411
, pp. 355-365
-
-
Blume-Jensen, P.1
Hunter, T.2
-
2
-
-
0026729382
-
The SH2 and SH3 domain-containing protein GRB2 links receptor tyrosine kinases to ras signaling
-
Lowenstein, E. J.; Daly, R. J.; Batzer, A. G.; Li, W.; Margolis, B.; Lammers, R.; Ullrich, A.; Skolnik, E. Y.; Bar-Sagi, D.; Schlessinger, J. The SH2 and SH3 domain-containing protein GRB2 links receptor tyrosine kinases to ras signaling. Cell 1992, 70, 431-442.
-
(1992)
Cell
, vol.70
, pp. 431-442
-
-
Lowenstein, E.J.1
Daly, R.J.2
Batzer, A.G.3
Li, W.4
Margolis, B.5
Lammers, R.6
Ullrich, A.7
Skolnik, E.Y.8
Bar-Sagi, D.9
Schlessinger, J.10
-
3
-
-
0028351583
-
Specific motifs recognized by the SH2 domains of Csk, 3BP2, fps/fes, GRB-2, HCP, SHC, Syk, and Vav
-
Songyang, Z.; Shoelson, S. E.; McGlade, J.; Olivier, P.; Pawson, T.; Bustelo, X. R.; Barbacid, M.; Sabe, H.; Hanafusa, H.; Yi, T. Specific motifs recognized by the SH2 domains of Csk, 3BP2, fps/fes, GRB-2, HCP, SHC, Syk, and Vav. Mol. Cell. Biol. 1994, 14, 2777-2785.
-
(1994)
Mol. Cell. Biol
, vol.14
, pp. 2777-2785
-
-
Songyang, Z.1
Shoelson, S.E.2
McGlade, J.3
Olivier, P.4
Pawson, T.5
Bustelo, X.R.6
Barbacid, M.7
Sabe, H.8
Hanafusa, H.9
Yi, T.10
-
4
-
-
0035161915
-
GRB2: A pivotal protein in signal transduction
-
Tari, A. M.; Lopez-Berestein, G. GRB2: A pivotal protein in signal transduction. Semin. Oncol. 2001, 28, 142-147.
-
(2001)
Semin. Oncol
, vol.28
, pp. 142-147
-
-
Tari, A.M.1
Lopez-Berestein, G.2
-
5
-
-
33745684525
-
p21-activated kinases in cancer
-
Kumar, R.; Gururaj, A. E.; Barnes, C. J. p21-activated kinases in cancer. Nat. Rev. Cancer 2006, 6, 459-471.
-
(2006)
Nat. Rev. Cancer
, vol.6
, pp. 459-471
-
-
Kumar, R.1
Gururaj, A.E.2
Barnes, C.J.3
-
6
-
-
0028609382
-
Integrin-mediated signal transduction linked to Ras pathway by GRB2 binding to focal adhesion kinase
-
Schlaepfer, D. D.; Hanks, S. K.; Hunter, T.; Van der Geer, P. Integrin-mediated signal transduction linked to Ras pathway by GRB2 binding to focal adhesion kinase. Nature 1994, 372, 786-791.
-
(1994)
Nature
, vol.372
, pp. 786-791
-
-
Schlaepfer, D.D.1
Hanks, S.K.2
Hunter, T.3
Van der Geer, P.4
-
7
-
-
33749188459
-
Intrinsic FAK activity and Y925 phosphorylation facilitate an angiogenic switch in tumors
-
Mitra, S. K.; Mikolon, D.; Molina, J. E.; Hsia, D. A.; Hanson, D. A.; Chi, A.; Lim, S. T.; Bernard-Trifilo, J. A.; Ilic, D.; Stupack, D. G.; Cheresh, D. A.; Schlaepfer, D. D. Intrinsic FAK activity and Y925 phosphorylation facilitate an angiogenic switch in tumors. Oncogene 2006, 25, 5969-5984.
-
(2006)
Oncogene
, vol.25
, pp. 5969-5984
-
-
Mitra, S.K.1
Mikolon, D.2
Molina, J.E.3
Hsia, D.A.4
Hanson, D.A.5
Chi, A.6
Lim, S.T.7
Bernard-Trifilo, J.A.8
Ilic, D.9
Stupack, D.G.10
Cheresh, D.A.11
Schlaepfer, D.D.12
-
8
-
-
21744435478
-
The role of focal-adhesion kinase in cancer - a new therapeutic opportunity
-
McLean, G. W.; Carragher, N. O.; Avizienyte, E.; Evans, J.; Brunton, V. G.; Frame, M. C. The role of focal-adhesion kinase in cancer - a new therapeutic opportunity. Nat. Rev. Cancer 2005, 5, 505-515.
-
(2005)
Nat. Rev. Cancer
, vol.5
, pp. 505-515
-
-
McLean, G.W.1
Carragher, N.O.2
Avizienyte, E.3
Evans, J.4
Brunton, V.G.5
Frame, M.C.6
-
9
-
-
33646104191
-
Molecular targeting of growth factor receptor-bound 2 (Grb2) as an anti-cancer strategy
-
Dharmawardana, P. G.; Peruzzi, B.; Giubellino, A.; Burke, J.; Bottaro, D. P. Molecular targeting of growth factor receptor-bound 2 (Grb2) as an anti-cancer strategy. Anti-Cancer Drugs 2006, 17, 13-20.
-
(2006)
Anti-Cancer Drugs
, vol.17
, pp. 13-20
-
-
Dharmawardana, P.G.1
Peruzzi, B.2
Giubellino, A.3
Burke, J.4
Bottaro, D.P.5
-
10
-
-
33645465610
-
Development of Grb2 SH2 domain signaling antagonists: A potential new class of antiproliferative agents
-
Burke, T. R. Development of Grb2 SH2 domain signaling antagonists: a potential new class of antiproliferative agents. Int. J. Pept. Res. Ther. 2006, 12, 33-48.
-
(2006)
Int. J. Pept. Res. Ther
, vol.12
, pp. 33-48
-
-
Burke, T.R.1
-
11
-
-
0035957990
-
Potent blockade of hepatocyte growth factor-stimulated cell motility, matrix invasion and branching morphogenesis by antagonists of Grb2 Src homology 2 domain interactions
-
Atabey, N.; Gao, Y.; Yao, Z. J.; Breckenridge, D.; Soon, L.; Soriano, J. V.; Burke, T. R.; Bottaro, D. P. Potent blockade of hepatocyte growth factor-stimulated cell motility, matrix invasion and branching morphogenesis by antagonists of Grb2 Src homology 2 domain interactions. J. Biol. Chem. 2001, 276, 14308-14314.
-
(2001)
J. Biol. Chem
, vol.276
, pp. 14308-14314
-
-
Atabey, N.1
Gao, Y.2
Yao, Z.J.3
Breckenridge, D.4
Soon, L.5
Soriano, J.V.6
Burke, T.R.7
Bottaro, D.P.8
-
12
-
-
7444229834
-
Inhibition of angiogenesis by growth factor receptor bound protein 2-Src homology 2 domain binding antagonists
-
Soriano, J. V.; Liu, N.; Gao, Y.; Yao, Z. Y.; Ishibashi, T.; Underhill, C.; Burke, T. R.; Bottaro, D. P. Inhibition of angiogenesis by growth factor receptor bound protein 2-Src homology 2 domain binding antagonists. Mol. Cancer Ther. 2004, 3, 1289-1299.
-
(2004)
Mol. Cancer Ther
, vol.3
, pp. 1289-1299
-
-
Soriano, J.V.1
Liu, N.2
Gao, Y.3
Yao, Z.Y.4
Ishibashi, T.5
Underhill, C.6
Burke, T.R.7
Bottaro, D.P.8
-
13
-
-
34447132249
-
Inhibition of tumor metastasis by a growth factor receptor bound protein 2 Src homology 2 domain-binding antagonist
-
Giubellino, A.; Gao, Y.; Lee, S.; Lee, M. J.; Vasselli, J. R.; Medepalli, S.; Trepel, J. B.; Burke, T. R.; Bottaro, D. P. Inhibition of tumor metastasis by a growth factor receptor bound protein 2 Src homology 2 domain-binding antagonist. Cancer Res. 2007, 67, 6012-6016.
-
(2007)
Cancer Res
, vol.67
, pp. 6012-6016
-
-
Giubellino, A.1
Gao, Y.2
Lee, S.3
Lee, M.J.4
Vasselli, J.R.5
Medepalli, S.6
Trepel, J.B.7
Burke, T.R.8
Bottaro, D.P.9
-
14
-
-
20344377158
-
Synthesis of a C-terminally biotinylated macrocyclic peptide mimetic exhibiting high Grb2 SH2 domain-binding affinity
-
Shi, Z. D.; Liu, H.; Zhang, M.; Worthy, K. M.; Bindu, L.; Yang, D.; Fisher, R. J.; Burke, T. R. Synthesis of a C-terminally biotinylated macrocyclic peptide mimetic exhibiting high Grb2 SH2 domain-binding affinity. Bioorg. Med. Chem. 2005, 13, 4200-4208.
-
(2005)
Bioorg. Med. Chem
, vol.13
, pp. 4200-4208
-
-
Shi, Z.D.1
Liu, H.2
Zhang, M.3
Worthy, K.M.4
Bindu, L.5
Yang, D.6
Fisher, R.J.7
Burke, T.R.8
-
15
-
-
0028074623
-
Rational design of Mn-salen catalyst (2): Highly enantioselective epoxidation of conjugated cis-olefins
-
Sasaki, H.; Irie, R.; Hamada, T.; Suzuki, K.; Katsuki, T. Rational design of Mn-salen catalyst (2): highly enantioselective epoxidation of conjugated cis-olefins. Tetrahedron 1994, 50, 11827-11838.
-
(1994)
Tetrahedron
, vol.50
, pp. 11827-11838
-
-
Sasaki, H.1
Irie, R.2
Hamada, T.3
Suzuki, K.4
Katsuki, T.5
-
16
-
-
0027769849
-
1,10-Phenanthroline derivatives: A new ligand class in the Heck reaction. Mechanistic aspects
-
Cabri, W.; Candiani, I.; Bedeschi, A.; Santi, R. 1,10-Phenanthroline derivatives: a new ligand class in the Heck reaction. Mechanistic aspects. J. Org. Chem. 1993, 58, 7421-7426.
-
(1993)
J. Org. Chem
, vol.58
, pp. 7421-7426
-
-
Cabri, W.1
Candiani, I.2
Bedeschi, A.3
Santi, R.4
-
17
-
-
0033955133
-
Stereoselective preparation of L-4- (2′-malonyl)phenylalanine suitably protected for Fmoc-based synthesis of potent signal transduction inhibitory ligands
-
Gao, Y.; Burke, T. R. Stereoselective preparation of L-4- (2′-malonyl)phenylalanine suitably protected for Fmoc-based synthesis of potent signal transduction inhibitory ligands. Synlett 2000, 134-136.
-
(2000)
Synlett
, pp. 134-136
-
-
Gao, Y.1
Burke, T.R.2
-
18
-
-
0028845294
-
Crystal structure of the SH2 domain from the adaptor protein SHC: A model for peptide binding based on X-ray and NMR data
-
Mikol, V.; Baumann, G.; Zurini, M. G. M.; Hommel, U. Crystal structure of the SH2 domain from the adaptor protein SHC: a model for peptide binding based on X-ray and NMR data. J. Mol. Biol. 1995, 254, 86-95.
-
(1995)
J. Mol. Biol
, vol.254
, pp. 86-95
-
-
Mikol, V.1
Baumann, G.2
Zurini, M.G.M.3
Hommel, U.4
-
19
-
-
20044370456
-
Evaluation of macrocyclic Grb2 SH2 domain-binding peptide mimetics prepared by ring-closing metathesis of C-terminal allylglycines with an N-terminal beta-vinyl-substituted phosphotyrosyl mimetic
-
Oishi, S.; Karki, R. G.; Shi, Z. D.; Worthy, K. M.; Bindu, L.; Chertov, O.; Esposito, D.; Frank, P.; Gillette, W. K.; Maderia, M.; Hartley, J.; Nicklaus, M. C.; Barchi, J.; Fisher, R. J.; Burke, T. R. Evaluation of macrocyclic Grb2 SH2 domain-binding peptide mimetics prepared by ring-closing metathesis of C-terminal allylglycines with an N-terminal beta-vinyl-substituted phosphotyrosyl mimetic. Bioorg. Med. Chem. 2005, 13, 2431-2438.
-
(2005)
Bioorg. Med. Chem
, vol.13
, pp. 2431-2438
-
-
Oishi, S.1
Karki, R.G.2
Shi, Z.D.3
Worthy, K.M.4
Bindu, L.5
Chertov, O.6
Esposito, D.7
Frank, P.8
Gillette, W.K.9
Maderia, M.10
Hartley, J.11
Nicklaus, M.C.12
Barchi, J.13
Fisher, R.J.14
Burke, T.R.15
-
20
-
-
0038660689
-
p21-activated kinase 1 (PAK1) interacts with the Grb2 adapter protein to couple to growth factor signaling
-
Puto, L. A.; Pestonjamasp, K.; King, C. C.; Bokoch, G. M. p21-activated kinase 1 (PAK1) interacts with the Grb2 adapter protein to couple to growth factor signaling. J. Biol. Chem. 2003, 278, 9388-9393.
-
(2003)
J. Biol. Chem
, vol.278
, pp. 9388-9393
-
-
Puto, L.A.1
Pestonjamasp, K.2
King, C.C.3
Bokoch, G.M.4
-
21
-
-
24044525271
-
Nuclear localization and chromatin targets of p21-activated kinase 1
-
Singh, R. R.; Song, C.; Yang, Z.; Kumar, R. Nuclear localization and chromatin targets of p21-activated kinase 1. J. Biol. Chem. 2005, 280, 18130-18137.
-
(2005)
J. Biol. Chem
, vol.280
, pp. 18130-18137
-
-
Singh, R.R.1
Song, C.2
Yang, Z.3
Kumar, R.4
-
22
-
-
34648828070
-
Modulation of p21-activated kinase 1 alters the behavior of renal cell carcinoma
-
O'Sullivan, G. C.; Tangney, M.; Casey, G.; Ambrose, M.; Houston, A.; Barry, O. P. Modulation of p21-activated kinase 1 alters the behavior of renal cell carcinoma. Int. J. Cancer 2007, 121, 1930-1940.
-
(2007)
Int. J. Cancer
, vol.121
, pp. 1930-1940
-
-
O'Sullivan, G.C.1
Tangney, M.2
Casey, G.3
Ambrose, M.4
Houston, A.5
Barry, O.P.6
-
23
-
-
34547734371
-
Sliding p21-activated kinase 1 to nucleus impacts tamoxifen sensitivity
-
Rayala, S. K.; Kumar, R. Sliding p21-activated kinase 1 to nucleus impacts tamoxifen sensitivity. Biomed. Pharmacother. 2007, 61, 408-411.
-
(2007)
Biomed. Pharmacother
, vol.61
, pp. 408-411
-
-
Rayala, S.K.1
Kumar, R.2
-
24
-
-
12844283323
-
The SH2 domain: Versatile signaling module and pharmaceutical target
-
Machida, K.; Mayer, B. J. The SH2 domain: versatile signaling module and pharmaceutical target. Biochim. Biophys. Actaica et Biophysica Acta, Proteins Proteomics 2005, 1747, 1-25.
-
(2005)
Biochim. Biophys. Actaica et Biophysica Acta, Proteins Proteomics
, vol.1747
, pp. 1-25
-
-
Machida, K.1
Mayer, B.J.2
-
25
-
-
0027403027
-
SH2 domains recognize specific phosphopeptide sequences
-
Songyang, Z.; Shoelson, S. E.; Chaudhuri, M.; Gish, G.; Pawson, T.; Haser, W. G.; King, F.; Roberts, T.; Ratnofsky, S.; Lechleider, R. J.; Neel, B. G.; Birge, R. B.; Fajardo, J. E.; Chou, M. M.; Hanafusa, H.; Schaffhausen, B.; Cantley, L. C. SH2 domains recognize specific phosphopeptide sequences. Cell 1993, 72, 767-778.
-
(1993)
Cell
, vol.72
, pp. 767-778
-
-
Songyang, Z.1
Shoelson, S.E.2
Chaudhuri, M.3
Gish, G.4
Pawson, T.5
Haser, W.G.6
King, F.7
Roberts, T.8
Ratnofsky, S.9
Lechleider, R.J.10
Neel, B.G.11
Birge, R.B.12
Fajardo, J.E.13
Chou, M.M.14
Hanafusa, H.15
Schaffhausen, B.16
Cantley, L.C.17
-
26
-
-
0034624812
-
Inhibition of Grb2 SH2 domain binding by non-phosphate- containing ligands 2. 4-(2-Malonyl)phenylalanine as a potent phosphotyrosyl mimetic
-
Gao, Y.; Luo, J.; Yao, Z.-J.; Guo, R.; Zou, H.; Kelley, J.; Voigt, J. H.; Yang, D.; Burke, T. R. Inhibition of Grb2 SH2 domain binding by non-phosphate- containing ligands 2. 4-(2-Malonyl)phenylalanine as a potent phosphotyrosyl mimetic. J. Med. Chem. 2000, 43, 911-920.
-
(2000)
J. Med. Chem
, vol.43
, pp. 911-920
-
-
Gao, Y.1
Luo, J.2
Yao, Z.-J.3
Guo, R.4
Zou, H.5
Kelley, J.6
Voigt, J.H.7
Yang, D.8
Burke, T.R.9
-
27
-
-
0032880670
-
Selective Grb2 SH2 inhibitors as anti-Ras therapy
-
Gay, B.; Suarez, S.; Caravatti, G.; Furet, P.; Meyer, T.; Schoepfer, J. Selective Grb2 SH2 inhibitors as anti-Ras therapy. Int. J. Cancer 1999, 83, 235-241.
-
(1999)
Int. J. Cancer
, vol.83
, pp. 235-241
-
-
Gay, B.1
Suarez, S.2
Caravatti, G.3
Furet, P.4
Meyer, T.5
Schoepfer, J.6
-
28
-
-
21044437830
-
Ring-closing metathesis of C-terminal allylglycine residues with an N-terminal beta-vinyl-substituted phosphotyrosyl mimetic as an approach to novel Grb2 SH2 domain-binding macrocyles
-
Oishi, S.; Shi, Z. D.; Worthy, K. M.; Bindu, L. K.; Fisher, R. J.; Burke, T. R. Ring-closing metathesis of C-terminal allylglycine residues with an N-terminal beta-vinyl-substituted phosphotyrosyl mimetic as an approach to novel Grb2 SH2 domain-binding macrocyles. ChemBioChem 2005, 6, 668-674.
-
(2005)
ChemBioChem
, vol.6
, pp. 668-674
-
-
Oishi, S.1
Shi, Z.D.2
Worthy, K.M.3
Bindu, L.K.4
Fisher, R.J.5
Burke, T.R.6
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