-
1
-
-
31144453233
-
BRAF mutation predicts sensitivity to MEK inhibition
-
Solit, D. B. et al. BRAF mutation predicts sensitivity to MEK inhibition. Nature 439, 358-362 (2006).
-
(2006)
Nature
, vol.439
, pp. 358-362
-
-
Solit, D.B.1
-
2
-
-
38049097938
-
Identification of genotype-correlated sensitivity to selective kinase inhibitors by using high-throughput tumor cell line profiling
-
McDermott, U. et al. Identification of genotype-correlated sensitivity to selective kinase inhibitors by using high-throughput tumor cell line profiling. Proc. Natl Acad. Sci. USA 104, 19936-19941 (2007).
-
(2007)
Proc. Natl Acad. Sci. USA
, vol.104
, pp. 19936-19941
-
-
McDermott, U.1
-
3
-
-
1942506706
-
V599EB-RAF is an oncogene in melanocytes
-
Wellbrock, C. et al. V599EB-RAF is an oncogene in melanocytes. Cancer Res. 64, 2338-2342 (2004).
-
(2004)
Cancer Res.
, vol.64
, pp. 2338-2342
-
-
Wellbrock, C.1
-
4
-
-
76149102749
-
Early efficacy signal demonstrated in advanced melanoma in a phase i trial of the oncogenic BRAF-selective inhibitor PLX4032
-
Chapman, P. et al. Early efficacy signal demonstrated in advanced melanoma in a phase I trial of the oncogenic BRAF-selective inhibitor PLX4032. Eur. J. Cancer 7 (suppl.), 5 (2009).
-
(2009)
Eur. J. Cancer
, vol.7
, Issue.SUPPL.5
-
-
Chapman, P.1
-
5
-
-
67651246671
-
Phase i study of PLX4032: Proof of concept for V600E BRAF mutation as a therapeutic target in human cancer
-
abstr
-
Flaherty, K. et al. Phase I study of PLX4032: Proof of concept for V600E BRAF mutation as a therapeutic target in human cancer. J. Clin. Oncol. 27 (suppl.), abstr. 9000 (2009).
-
(2009)
J. Clin. Oncol.
, vol.27
, Issue.SUPPL.
, pp. 9000
-
-
Flaherty, K.1
-
6
-
-
42949149240
-
Discovery of a selective inhibitor of oncogenic B-Raf kinase with potent antimelanoma activity
-
Tsai, J. et al. Discovery of a selective inhibitor of oncogenic B-Raf kinase with potent antimelanoma activity. Proc. Natl Acad. Sci. USA 105, 3041-3046 (2008).
-
(2008)
Proc. Natl Acad. Sci. USA
, vol.105
, pp. 3041-3046
-
-
Tsai, J.1
-
7
-
-
8444238236
-
The RAF proteins take centre stage
-
Wellbrock, C., Karasarides, M. & Marais, R. The RAF proteins take centre stage. Nature Rev. Mol. Cell Biol. 5, 875-885 (2004).
-
(2004)
Nature Rev. Mol. Cell Biol.
, vol.5
, pp. 875-885
-
-
Wellbrock, C.1
Karasarides, M.2
Marais, R.3
-
8
-
-
67649770887
-
Ras signaling and therapies
-
Young, A. et al. Ras signaling and therapies. Adv. Cancer Res. 102, 1-17 (2009).
-
(2009)
Adv. Cancer Res.
, vol.102
, pp. 1-17
-
-
Young, A.1
-
9
-
-
32944461545
-
Activity of the dual kinase inhibitor lapatinib (GW572016) against HER-2-overexpressing and trastuzumab-treated breast cancer cells
-
Konecny, G. E. et al. Activity of the dual kinase inhibitor lapatinib (GW572016) against HER-2-overexpressing and trastuzumab-treated breast cancer cells. Cancer Res. 66, 1630-1639 (2006).
-
(2006)
Cancer Res.
, vol.66
, pp. 1630-1639
-
-
Konecny, G.E.1
-
10
-
-
0035328521
-
Active Ras induces heterodimerization of cRaf and BRaf
-
Weber, C. K., Slupsky, J. R., Kalmes, H. A. & Rapp, U. R. Active Ras induces heterodimerization of cRaf and BRaf. Cancer Res. 61, 3595-3598 (2001).
-
(2001)
Cancer Res.
, vol.61
, pp. 3595-3598
-
-
Weber, C.K.1
Slupsky, J.R.2
Kalmes, H.A.3
Rapp, U.R.4
-
11
-
-
12144289677
-
Mechanism of activation of the RAF-ERK signaling pathway by oncogenic mutations of B-RAF
-
Wan, P. T. et al. Mechanism of activation of the RAF-ERK signaling pathway by oncogenic mutations of B-RAF. Cell 116, 855-867 (2004).
-
(2004)
Cell
, vol.116
, pp. 855-867
-
-
Wan, P.T.1
-
12
-
-
33644786244
-
Regulation and role of Raf-1/B-Raf heterodimerization
-
Rushworth, L. K., Hindley, A. D., O'Neill, E. & Kolch, W. Regulation and role of Raf-1/B-Raf heterodimerization. Mol. Cell. Biol. 26, 2262-2272 (2006).
-
(2006)
Mol. Cell. Biol.
, vol.26
, pp. 2262-2272
-
-
Rushworth, L.K.1
Hindley, A.D.2
O'Neill, E.3
Kolch, W.4
-
13
-
-
13144279271
-
Autoregulation of the Raf-1 serine/threonine kinase
-
Cutler, R. E. Jr, Stephens, R. M., Saracino, M. R. & Morrison, D. K. Autoregulation of the Raf-1 serine/threonine kinase. Proc. Natl Acad. Sci. USA 95, 9214-9219 (1998).
-
(1998)
Proc. Natl Acad. Sci. USA
, vol.95
, pp. 9214-9219
-
-
Cutler Jr., R.E.1
Stephens, R.M.2
Saracino, M.R.3
Morrison, D.K.4
-
14
-
-
67650337799
-
Inhibitor hijacking of Akt activation
-
Okuzumi, T. et al. Inhibitor hijacking of Akt activation. Nature Chem. Biol. 5, 484-493 (2009).
-
(2009)
Nature Chem. Biol.
, vol.5
, pp. 484-493
-
-
Okuzumi, T.1
-
15
-
-
67349125149
-
PKC maturation is promoted by nucleotide pocket occupation independently of intrinsic kinase activity
-
Cameron, A. J., Escribano, C., Saurin, A. T., Kostelecky, B. & Parker, P. J. PKC maturation is promoted by nucleotide pocket occupation independently of intrinsic kinase activity. Nature Struct. Mol. Biol. 16, 624-630 (2009).
-
(2009)
Nature Struct. Mol. Biol.
, vol.16
, pp. 624-630
-
-
Cameron, A.J.1
Escribano, C.2
Saurin, A.T.3
Kostelecky, B.4
Parker, P.J.5
-
16
-
-
70449123573
-
C-Raf inhibits MAPK activation and transformation by B-Raf(V600E)
-
Karreth, F. A., DeNicola, G. M., Winter, S. P. & Tuveson, D. A. C-Raf inhibits MAPK activation and transformation by B-Raf(V600E). Mol. Cell 36, 477-486 (2009).
-
(2009)
Mol. Cell
, vol.36
, pp. 477-486
-
-
Karreth, F.A.1
Denicola, G.M.2
Winter, S.P.3
Tuveson, D.A.4
-
17
-
-
33947317223
-
Structure-guided development of affinity probes for tyrosine kinases using chemical genetics
-
Blair, J. A. et al. Structure-guided development of affinity probes for tyrosine kinases using chemical genetics. Nature Chem. Biol. 3, 229-238 (2007).
-
(2007)
Nature Chem. Biol.
, vol.3
, pp. 229-238
-
-
Blair, J.A.1
-
18
-
-
0033023489
-
Growth inhibition of nasopharyngeal carcinoma cells by EGF receptor tyrosine kinase inhibitors
-
Sun, Y. et al. Growth inhibition of nasopharyngeal carcinoma cells by EGF receptor tyrosine kinase inhibitors. Anticancer Res. 19, 919-924 (1999).
-
(1999)
Anticancer Res.
, vol.19
, pp. 919-924
-
-
Sun, Y.1
-
19
-
-
70349438995
-
A dimerization-dependent mechanism drives RAF catalytic activation
-
Rajakulendran, T., Sahmi, M., Lefrancois, M., Sicheri, F. & Therrien, M. A dimerization-dependent mechanism drives RAF catalytic activation. Nature 461, 542-545 (2009).
-
(2009)
Nature
, vol.461
, pp. 542-545
-
-
Rajakulendran, T.1
Sahmi, M.2
Lefrancois, M.3
Sicheri, F.4
Therrien, M.5
-
20
-
-
0033179479
-
Paradoxical activation of Raf by a novel Raf inhibitor
-
Hall-Jackson, C. A. et al. Paradoxical activation of Raf by a novel Raf inhibitor. Chem. Biol. 6, 559-568 (1999).
-
(1999)
Chem. Biol.
, vol.6
, pp. 559-568
-
-
Hall-Jackson, C.A.1
-
21
-
-
33845730781
-
Demonstration of a genetic therapeutic index for tumors expressing oncogenic BRAF by the kinase inhibitor SB-590885
-
King, A. J. et al. Demonstration of a genetic therapeutic index for tumors expressing oncogenic BRAF by the kinase inhibitor SB-590885. Cancer Res. 66, 11100-11105 (2006).
-
(2006)
Cancer Res.
, vol.66
, pp. 11100-11105
-
-
King, A.J.1
-
22
-
-
66149126085
-
V600Emutational status and sustained extracellular signal-regulated kinase/mitogen-activated protein kinase pathway suppression
-
Hoeflich, K. P. et al. Antitumor efficacy of the novel RAF inhibitor GDC-0879 is predicted by BRAFV600E mutational status and sustained extracellular signal-regulated kinase/mitogen-activated protein kinase pathway suppression. Cancer Res. 69, 3042-3051 (2009).
-
(2009)
Cancer Res.
, vol.69
, pp. 3042-3051
-
-
Hoeflich, K.P.1
-
23
-
-
74849109743
-
Kinase-dead BRAF and oncogenic RAS cooperate to drive tumor progression through CRAF
-
Heidorn, S. J. et al. Kinase-dead BRAF and oncogenic RAS cooperate to drive tumor progression through CRAF. Cell 140, 209-221 (2010).
-
(2010)
Cell
, vol.140
, pp. 209-221
-
-
Heidorn, S.J.1
-
24
-
-
65649108998
-
AZD6244 (ARRY-142886) vs temozolomide (TMZ) in patients (pts) with advanced melanoma: An open-label, randomized, multicenter, phase II study
-
abstr
-
Dummer, R. et al. AZD6244 (ARRY-142886) vs temozolomide (TMZ) in patients (pts) with advanced melanoma: An open-label, randomized, multicenter, phase II study. J. Clin. Oncol. 26 (suppl.), abstr. 9033 (2008).
-
(2008)
J. Clin. Oncol.
, vol.26
, Issue.SUPPL.
, pp. 9033
-
-
Dummer, R.1
-
25
-
-
49649118852
-
Elevated CRAF as a potential mechanism of acquired resistance to BRAF inhibition in melanoma
-
Montagut, C. et al. Elevated CRAF as a potential mechanism of acquired resistance to BRAF inhibition in melanoma. Cancer Res. 68, 4853-4861 (2008).
-
(2008)
Cancer Res.
, vol.68
, pp. 4853-4861
-
-
Montagut, C.1
-
26
-
-
0036857484
-
A scaleable synthesis of BAY 43-9006: A potent Raf kinase inhibitor for the treatment of cancer
-
Bankston, D. et al. A scaleable synthesis of BAY 43-9006: A potent Raf kinase inhibitor for the treatment of cancer. Org. Process Res. Dev. 6, 777-781 (2002).
-
(2002)
Org. Process Res. Dev.
, vol.6
, pp. 777-781
-
-
Bankston, D.1
|