-
1
-
-
0034762203
-
The Raf/MEK/ERK pathway: New concepts of activation
-
DOI 10.1016/S0248-4900(01)01125-X
-
Peyssonnaux, C.; Eychene, A. The Raf/MEK/ERK pathway: New concepts of activation Biol. Cell. 2001, 93, 53-62 (Pubitemid 33040860)
-
(2001)
Biology of the Cell
, vol.93
, Issue.1-2
, pp. 53-62
-
-
Peyssonnaux, C.1
Eychene, A.2
-
2
-
-
18444374405
-
Mutations of the BRAF gene in human cancer
-
DOI 10.1038/nature00766
-
Davies, H.; Bignell, G. R.; Cox, C.; Stephens, P.; Edkins, S.; Clegg, S.; Teague, J.; Woffendin, H.; Garnett, M. J.; Bottomley, W.; Davis, N.; Dicks, E.; Ewing, R.; Floyd, Y.; Gray, K.; Hall, S.; Hawes, R.; Hughes, J.; Kosmidou, V.; Menzies, A.; Mould, C.; Parker, A.; Stevens, C.; Watt, S.; Hooper, S.; Wilson, R.; Jayatilake, H.; Gusterson, B. A.; Cooper, C.; Shipley, J.; Hargrave, D.; Pritchard-Jones, K.; Maitland, N.; Chenevix-Trench, G.; Riggins, G. J.; Bigner, D. D.; Palmieri, G.; Cossu, A.; Flanagan, A.; Nicholson, A.; Ho, J. W. C.; Leung, S. Y.; Yuen, S. T.; Weber, B. L.; Seigler, H. F.; Darrow, T. L.; Paterson, H.; Marais, R.; Marshall, C. J.; Wooster, R.; Stratton, M. R.; Futreal, P. A. Mutations of the BRAF gene in human cancer Nature 2002, 417, 949-954 (Pubitemid 34716871)
-
(2002)
Nature
, vol.417
, Issue.6892
, pp. 949-954
-
-
Davies, H.1
Bignell, G.R.2
Cox, C.3
Stephens, P.4
Edkins, S.5
Clegg, S.6
Teague, J.7
Woffendin, H.8
Garnett, M.J.9
Bottomley, W.10
Davis, N.11
Dicks, E.12
Ewing, R.13
Floyd, Y.14
Gray, K.15
Hall, S.16
Hawes, R.17
Hughes, J.18
Kosmidou, V.19
Menzies, A.20
Mould, C.21
Parker, A.22
Stevens, C.23
Watt, S.24
Hooper, S.25
Wilson, R.26
Jayatilake, H.27
Gusterson, B.A.28
Cooper, C.29
Shipley, J.30
Hargrave, D.31
Pritchard-Jones, K.32
Maitland, N.33
Chenevix-Trench, G.34
Riggins, G.J.35
Bigner, D.D.36
Palmleri, G.37
Cossu, A.38
Flanagan, A.39
Nicholson, A.40
Ho, J.W.C.41
Leung, S.Y.42
Yuen, S.T.43
Weber, B.L.44
Seigler, H.F.45
Darrow, T.L.46
Paterson, H.47
Marais, R.48
Marshall, C.J.49
Wooster, R.50
Stratton, M.R.51
Futreal, P.A.52
more..
-
3
-
-
0037228055
-
High frequency of BRAF mutations in nevi
-
DOI 10.1038/ng1054
-
Pollock., P. M.; Harper, U. L.; Hansen, K. S.; Yudt, L. M.; Stark, M.; Robbins, C. M.; Moses, T. Y.; Hostetter, G.; Wagner, U.; Kakereka, J.; Salem, G.; Pohida, T.; Heenean, P.; Duray, P.; Kallioniemi, O.; Hayward, N. K.; Trent, J. M.; Meltzer, P. S. High frequency of B-Raf mutations in nevi Nat. Genet. 2003, 33, 19-20 (Pubitemid 36068675)
-
(2003)
Nature Genetics
, vol.33
, Issue.1
, pp. 19-20
-
-
Pollock, P.M.1
Harper, U.L.2
Hansen, K.S.3
Yudt, L.M.4
Stark, M.5
Robbins, C.M.6
Moses, T.Y.7
Hostetter, G.8
Wagner, U.9
Kakareka, J.10
Salem, G.11
Pohida, T.12
Heenan, P.13
Duray, P.14
Kallioniemi, O.15
Hayward, N.K.16
Trent, J.M.17
Meltzer, P.S.18
-
4
-
-
0042173193
-
Analysis of BRAF and N-RAS mutations in metastatic melanoma tissues
-
Gorden, A.; Osman, I.; Gai, W.; He, D.; Huang, W.; Davidson, A.; Houghton, A. N.; Busam, K.; Polsky, D. Analysis of B-Raf and N-Ras mutations in metastatic melanoma tissues Cancer Res. 2003, 63, 3955-3957 (Pubitemid 36917911)
-
(2003)
Cancer Research
, vol.63
, Issue.14
, pp. 3955-3957
-
-
Gorden, A.1
Osman, I.2
Gai, W.3
He, D.4
Huang, W.5
Davidson, A.6
Houghton, A.N.7
Busam, K.8
Polsky, D.9
-
5
-
-
0041333110
-
BRAF mutations in metastatic melanoma: A possible association with clinical outcome
-
Kuman, R.; Angelini, S.; Czene, K.; Sauroja, I.; Hahka-Kemppinen, M.; Pyrhonen, S.; Hemminki, K. B-Raf mutations in metastatic melanoma: A possible association with clinical outcome Clin. Cancer Res. 2003, 9, 3362-3368 (Pubitemid 37082731)
-
(2003)
Clinical Cancer Research
, vol.9
, Issue.9
, pp. 3362-3368
-
-
Kumar, R.1
Angelini, S.2
Czene, K.3
Sauroja, I.4
Hahka-Kemppinen, M.5
Pyrhonen, S.6
Hemminki, K.7
-
6
-
-
39149083748
-
New insights in thyroid follicular cell biology and its impact in thyroid cancer therapy
-
DOI 10.1677/ERC-07-0085
-
Riesco-Eizaguirre, G.; Santisteban, P. New insights in thyroid follicular cell biology and its impact in thyroid cancer therapy Endocr.-Relat. Cancer 2007, 14, 957-977 (Pubitemid 351252429)
-
(2007)
Endocrine-Related Cancer
, vol.14
, Issue.4
, pp. 957-977
-
-
Riesco-Eizaguirre, G.1
Santisteban, P.2
-
7
-
-
70350364867
-
Targeting of the BRAF gene in papillary thyroid carcinoma (Review)
-
Li, Y.; Nakamura, M.; Kakudo, K. Targeting of the BRAF gene in papillary thyroid carcinoma (Review) Oncol. Rep. 2009, 22, 671-681
-
(2009)
Oncol. Rep.
, vol.22
, pp. 671-681
-
-
Li, Y.1
Nakamura, M.2
Kakudo, K.3
-
8
-
-
0037624602
-
Mutations of the BRAF gene in cholangiocarcinoma but not in hepatocellular carcinoma
-
DOI 10.1136/gut.52.5.706
-
Tannapfel, A.; Sommerer, F.; Benicke, M.; Katalinic, A.; Uhlmann, D.; Witzigmann, H.; Hauss, J.; Wittekind, C. Mutations of the BRAF gene in cholangiocarcinoma but not in hepatocellular carcinoma Gut 2003, 52, 706-712 (Pubitemid 36528874)
-
(2003)
Gut
, vol.52
, Issue.5
, pp. 706-712
-
-
Tannapfel, A.1
Sommerer, F.2
Benicke, M.3
Katalinic, A.4
Uhlmann, D.5
Witzigmann, H.6
Hauss, J.7
Wittekind, C.8
-
9
-
-
12144289677
-
Mechanism of activation of the RAF-ERK signaling pathway by oncogenic mutations of B-RAF
-
DOI 10.1016/S0092-8674(04)00215-6, PII S0092867404002156
-
Wan, P. T.; Garnett, M. J.; Roe, S. M.; Lee, S.; Niculescu-Duvaz, D.; Good, V. M.; Jones, C. M.; Marshall, C. J.; Springer, C. J.; Barford, D.; Marais, R. Mechanism of activation of the RAF-ERK signaling pathway by oncogenic mutations of B-RAF Cell 2004, 116, 855-867 (Pubitemid 38410730)
-
(2004)
Cell
, vol.116
, Issue.6
, pp. 855-867
-
-
Wan, P.T.C.1
Garnett, M.J.2
Roe, S.M.3
Lee, S.4
Niculescu-Duvaz, D.5
Good, V.M.6
Project, C.G.7
Jones, C.M.8
Marshall, C.J.9
Springer, C.J.10
Barford, D.11
Marais, R.12
-
10
-
-
22244472992
-
Poor survival associated with the BRAF V600E mutation in microsatellite-stable colon cancers
-
Samowitz, W. S.; Sweeney, C.; Herrick, J.; Albertsen, H.; Levin, T. R.; Murtaugh, M. A.; Wolff, R. K.; Slattery, M. L. Poor survival associated with the BRAF V600E mutation in microsatellite-stable colon cancers Cancer Res. 2005, 65, 6063-6069
-
(2005)
Cancer Res.
, vol.65
, pp. 6063-6069
-
-
Samowitz, W.S.1
Sweeney, C.2
Herrick, J.3
Albertsen, H.4
Levin, T.R.5
Murtaugh, M.A.6
Wolff, R.K.7
Slattery, M.L.8
-
11
-
-
33645964942
-
The oncogene BRAF V600E is associated with a high risk of recurrence and less differentiated papillary thyroid carcinoma due to the impairment of Na+/I-targeting to the membrane
-
Riesco-Eizaguirre, G.; Gutierrez-Martinez, P.; Garcia-Cabezas, M. A.; Mistal, M.; Santisteban, P. The oncogene BRAF V600E is associated with a high risk of recurrence and less differentiated papillary thyroid carcinoma due to the impairment of Na+/I-targeting to the membrane Endocr.-Relat. Cancer 2006, 13, 257-269
-
(2006)
Endocr.-Relat. Cancer
, vol.13
, pp. 257-269
-
-
Riesco-Eizaguirre, G.1
Gutierrez-Martinez, P.2
Garcia-Cabezas, M.A.3
Mistal, M.4
Santisteban, P.5
-
12
-
-
2942607408
-
Constitutive activation of the Ras-Raf signaling pathway in metastatic melanoma is associated with poor prognosis
-
Houben, R.; Becker, J. C.; Kappel, A.; Terheyden, P.; Bröcker, E. B.; Goetz, R.; Rapp, U. R. Constitutive activation of the Ras-Raf signaling pathway in metastatic melanoma is associated with poor prognosis J. Carcinog. 2004, 3, 6-18
-
(2004)
J. Carcinog.
, vol.3
, pp. 6-18
-
-
Houben, R.1
Becker, J.C.2
Kappel, A.3
Terheyden, P.4
Bröcker, E.B.5
Goetz, R.6
Rapp, U.R.7
-
13
-
-
9244222261
-
Targeted cancer therapy
-
DOI 10.1038/nature03095
-
Sawyers, C. Targeted cancer therapy Nature 2004, 432, 294-297 (Pubitemid 39551656)
-
(2004)
Nature
, vol.432
, Issue.7015
, pp. 294-297
-
-
Sawyers, C.1
-
14
-
-
67649726156
-
Protein kinase inhibitors: Contributions from structure to clinical compounds
-
Johnson, L. N. Protein kinase inhibitors: Contributions from structure to clinical compounds Q. Rev. Biophys. 2009, 42, 1-40
-
(2009)
Q. Rev. Biophys.
, vol.42
, pp. 1-40
-
-
Johnson, L.N.1
-
15
-
-
79956101161
-
-
ClinicalTrials.gov web site. (accessed Feb 22). A study to evaluate RAF265, an oral drug administered to subjects with locally advanced or metastatic melanoma.
-
ClinicalTrials.gov web site. http://www.clinicaltrials.gov (accessed Feb 22, 2011). A study to evaluate RAF265, an oral drug administered to subjects with locally advanced or metastatic melanoma.
-
(2011)
-
-
-
16
-
-
68949106943
-
A phase i study of XL281, a selective oral RAF kinase inhibitor, in patients (Pts) with advanced solid tumors
-
Abstr. 3513
-
Schwartz, G. L.; Robertson, S.; Shen, A.; Wang, E.; Pace, L.; Dials, H.; Mendelson, D.; Shannon, P.; Gordon, M. A phase I study of XL281, a selective oral RAF kinase inhibitor, in patients (Pts) with advanced solid tumors J. Clin. Oncol. 2009, 27, 15s Abstr. 3513
-
(2009)
J. Clin. Oncol.
, vol.27
-
-
Schwartz, G.L.1
Robertson, S.2
Shen, A.3
Wang, E.4
Pace, L.5
Dials, H.6
Mendelson, D.7
Shannon, P.8
Gordon, M.9
-
17
-
-
77957350123
-
Phase I/II study of GSK2118436, a selective inhibitor of oncogenic mutant BRAF kinase, in patients with metastatic melanoma and other solid tumors
-
Abstr. 8503
-
Kefford, R.; Arkenau, H.; Brown, M. P.; Millward, M.; Infante, J. R.; Long, G. V.; Ouellet, D.; Curtis, M.; Lebowitz, P. F.; Falchook, G. S. Phase I/II study of GSK2118436, a selective inhibitor of oncogenic mutant BRAF kinase, in patients with metastatic melanoma and other solid tumors J. Clin Oncol. 2010, 28, 15s Abstr. 8503
-
(2010)
J. Clin Oncol.
, vol.28
-
-
Kefford, R.1
Arkenau, H.2
Brown, M.P.3
Millward, M.4
Infante, J.R.5
Long, G.V.6
Ouellet, D.7
Curtis, M.8
Lebowitz, P.F.9
Falchook, G.S.10
-
18
-
-
77956030786
-
Inhibition of mutated, activated BRAF in metastatic melanoma
-
Flaherty, K. T.; Puzanov, I.; Kim, K. B.; Ribas, A.; McArthur, G. A.; Sosman, J. A.; O'Dwyer, P. J.; Lee, R. J.; Grippo, J. F.; Nolop, K.; Chapman, P. B. Inhibition of mutated, activated BRAF in metastatic melanoma N. Engl. J. Med. 2010, 363, 809-819
-
(2010)
N. Engl. J. Med.
, vol.363
, pp. 809-819
-
-
Flaherty, K.T.1
Puzanov, I.2
Kim, K.B.3
Ribas, A.4
McArthur, G.A.5
Sosman, J.A.6
O'Dwyer, P.J.7
Lee, R.J.8
Grippo, J.F.9
Nolop, K.10
Chapman, P.B.11
-
19
-
-
33845730781
-
Demonstration of a genetic therapeutic index for tumors expressing oncogenic BRAF by the kinase inhibitor SB-590885
-
DOI 10.1158/0008-5472.CAN-06-2554
-
King, A. J.; Patrick, D. R.; Batorsky, R. S.; Ho, M. L; Do, H. T.; Zhang, S. Y.; Kumar, R.; Rusnak, D. W.; Takle, A. K.; Wilson, D. M.; Hugger, E.; Wang, L.; Karreth, F.; Lougheed, J. C.; Lee, J.; Chau, D.; Stout, T. J.; May, E. W.; Rominger, C.; M.; Schaber, M.; D.; Luo, L.; Lakdawala, A. S.; Adams, J. L.; Contractor, R. G.; Smalley, K. S. M.; Herlyn, M.; Morrissey, M. M.; Tuveson, D. A.; Huang, P. S. Demonstration of a Genetic Therapeutic Index for Tumors Expressing Oncogenic BRAF by the Kinase Cancer Res. 2006, 66, 11100-11105 (Pubitemid 46009933)
-
(2006)
Cancer Research
, vol.66
, Issue.23
, pp. 11100-11105
-
-
King, A.J.1
Patrick, D.R.2
Batorsky, R.S.3
Ho, M.L.4
Do, H.T.5
Zhang, S.Y.6
Kumar, R.7
Rusnak, D.W.8
Takle, A.K.9
Wilson, D.M.10
Hugger, E.11
Wang, L.12
Karreth, F.13
Lougheed, J.C.14
Lee, J.15
Chau, D.16
Stout, T.J.17
May, E.W.18
Rominger, C.M.19
Schaber, M.D.20
Luo, L.21
Lakdawala, A.S.22
Adams, J.L.23
Contractor, R.G.24
Smalley, K.S.M.25
Herlyn, M.26
Morrissey, M.M.27
Tuveson, D.A.28
Huang, P.S.29
more..
-
20
-
-
66149126085
-
V600E mutational status and sustained extracellular signal-regulated kinase/mitogen-activated protein kinase pathway suppression
-
V600E mutational status and sustained extracellular signal-regulated kinase/mitogen-activated protein kinase pathway suppression Cancer Res. 2009, 69, 3042-3051
-
(2009)
Cancer Res.
, vol.69
, pp. 3042-3051
-
-
Hoeflich, K.P.1
Herter, S.2
Tien, J.3
Wong, L.4
Berru, L.5
Chan, J.6
O'Brien, C.7
Modrusan, Z.8
Seshagiri, S.9
Lackner, M.10
Stern, H.11
Choo, E.12
Murray, L.13
Friedman, L.S.14
Belvin, M.15
-
21
-
-
48649100604
-
Knowledge-based design of 7-azaindoles as selective B-Raf inhibitors
-
Tang, J.; Hamajima, T.; Nakano, M.; Sato, H.; Dickerson, S. H.; Lackey, K. E. Knowledge-based design of 7-azaindoles as selective B-Raf inhibitors Bioorg. Med. Chem. Lett. 2008, 18, 4610-4614
-
(2008)
Bioorg. Med. Chem. Lett.
, vol.18
, pp. 4610-4614
-
-
Tang, J.1
Hamajima, T.2
Nakano, M.3
Sato, H.4
Dickerson, S.H.5
Lackey, K.E.6
-
22
-
-
70350061746
-
Selective inhibitors of the mutant B-Raf pathway: Discovery of a potent and orally bioavailable aminoisoquinoline
-
Smith, A. L.; DeMorin, F. F.; Paras, M. A.; Huang, Q.; Petkus, J. K.; Doherty, E. M.; Nixey, T.; Kim, J. L.; Whittington, D. A.; Epstein, L. F.; Lee, M. R.; Rose, M. J.; Babij, C.; Fernando, M.; Hess, K.; Le, Q.; Beltran, P.; Carnahan, J. Selective inhibitors of the mutant B-Raf pathway: Discovery of a potent and orally bioavailable aminoisoquinoline J. Med. Chem. 2009, 52, 6289-6292
-
(2009)
J. Med. Chem.
, vol.52
, pp. 6289-6292
-
-
Smith, A.L.1
Demorin, F.F.2
Paras, M.A.3
Huang, Q.4
Petkus, J.K.5
Doherty, E.M.6
Nixey, T.7
Kim, J.L.8
Whittington, D.A.9
Epstein, L.F.10
Lee, M.R.11
Rose, M.J.12
Babij, C.13
Fernando, M.14
Hess, K.15
Le, Q.16
Beltran, P.17
Carnahan, J.18
-
23
-
-
77956513286
-
Clinical efficacy of a RAF inhibitor needs broad target blockade in BRAF-mutant melanoma
-
Bollag, G.; Hirth, P.; Tsai, J.; Zhang, J.; Ibrahim, P. N.; Cho, H.; Spevak, W.; Zhang, C.; Zhang, Y.; Habets, G.; Burton, E. A.; Wong, B.; Tsang, G.; West., B. L.; Powell, B.; Shellooe, R.; Marimuthu, A.; Nguyen, H.; Zhang, K. Y. J.; Artis, D. R.; Schlessinger, J.; Su, F.; Higgins, B.; Iyer, R.; D'Andrea, K.; Koehler, A.; Stumm, M.; Lin., P. S.; Lee, R. J.; Grippo, J.; Puzanov, I.; Kim, K. B.; Ribas, A.; McArthur, G. A.; Sosman, J. A.; Chapman, P. B.; Flaherty, K. T.; Xu, X.; Nathanson, K. L.; Nolop, K. Clinical efficacy of a RAF inhibitor needs broad target blockade in BRAF-mutant melanoma Nature 2010, 467, 596-599
-
(2010)
Nature
, vol.467
, pp. 596-599
-
-
Bollag, G.1
Hirth, P.2
Tsai, J.3
Zhang, J.4
Ibrahim, P.N.5
Cho, H.6
Spevak, W.7
Zhang, C.8
Zhang, Y.9
Habets, G.10
Burton, E.A.11
Wong, B.12
Tsang, G.13
West, B.L.14
Powell, B.15
Shellooe, R.16
Marimuthu, A.17
Nguyen, H.18
Zhang, K.Y.J.19
Artis, D.R.20
Schlessinger, J.21
Su, F.22
Higgins, B.23
Iyer, R.24
D'Andrea, K.25
Koehler, A.26
Stumm, M.27
Lin, P.S.28
Lee, R.J.29
Grippo, J.30
Puzanov, I.31
Kim, K.B.32
Ribas, A.33
McArthur, G.A.34
Sosman, J.A.35
Chapman, P.B.36
Flaherty, K.T.37
Xu, X.38
Nathanson, K.L.39
Nolop, K.40
more..
-
24
-
-
4644289313
-
A unique structure for epidermal growth factor receptor bound to GW572016 (Lapatinib): Relationships among protein conformation, inhibitor off-rate, and receptor activity in tumor cells
-
DOI 10.1158/0008-5472.CAN-04-1168
-
Via a substituted benzyl ether, lapatinib also traps a shifted αC-helix in EGFR kinase, which similarly leads to high kinase selectivity: Wood, E. R.; Truesdale, A. T.; McDonald, O. B.; Yuan, D.; Hassell, A.; Dickerson, S. H.; Ellis, B.; Pennisi, C.; Horne, E.; Lackey, K.; Alligood, K. J.; Rusnak, D. W.; Gilmer, T. M.; Shewchuk, L. A unique structure for epidermal growth factor receptor bound to GW572016 (lapatinib): Relationships among protein conformation, inhibitor off-rate, and receptor activity in tumor cells Cancer Res. 2004, 64, 6652-6659 (Pubitemid 39297926)
-
(2004)
Cancer Research
, vol.64
, Issue.18
, pp. 6652-6659
-
-
Wood, E.R.1
Truesdale, A.T.2
McDonald, O.B.3
Yuan, D.4
Hassell, A.5
Dickerson, S.H.6
Ellis, B.7
Pennisi, C.8
Horne, E.9
Lackey, K.10
Alligood, K.J.11
Rusnak, D.W.12
Gilmer, T.M.13
Shewchuk, L.14
-
25
-
-
79956080960
-
-
WO 2009/111279.
-
Ahrendt, K. A.; Buckmelter, A. J.; De Meese, J.; Grina, J.; Hansen, J. D.; Laird, E. R.; Lunghofer, P.; Moreno, D.; Newhouse, B.; Ren, L.; Seo, J.; Tian, H.; Wenglowsky, S. M.; Feng, B.; Gunzner, J.; Malesky, K.; Mathieu, S.; Rudolph, J.; Wen, Z.; Young, W. B. N-Pyrazolo[3,4-b]pyridinyl benzamide derivatives as Raf inhibitors and their preparation, pharmaceutical compositions and use in the treatment of diseases. WO 2009/111279.
-
N-Pyrazolo[3,4-b]pyridinyl Benzamide Derivatives As Raf Inhibitors and Their Preparation, Pharmaceutical Compositions and Use in the Treatment of Diseases
-
-
Ahrendt, K.A.1
Buckmelter, A.J.2
De Meese, J.3
Grina, J.4
Hansen, J.D.5
Laird, E.R.6
Lunghofer, P.7
Moreno, D.8
Newhouse, B.9
Ren, L.10
Seo, J.11
Tian, H.12
Wenglowsky, S.M.13
Feng, B.14
Gunzner, J.15
Malesky, K.16
Mathieu, S.17
Rudolph, J.18
Wen, Z.19
Young, W.B.20
more..
-
26
-
-
31544446922
-
Potent and selective mitogen-activated protein kinase kinase (MEK) 1,2 inhibitors. 1. 4-(4-bromo-2-fluorophenylamino)-1-methylpyridin-2(1h)-ones
-
DOI 10.1021/jm050834y
-
Wallace, E. M.; Lyssikatos, J.; Blake, J. F.; Seo, J.; Yang, H. W.; Yeh, T. C.; Perrier, M.; Jarski, H.; Marsh, V.; Poch, G.; Livingston, M. G.; Otten, J.; Hingorani, G.; Woessner, R.; Lee, P.; Winkler, J.; Koch, K. Potent and selective mitogen-activated protein kinase kinase (MEK) 1,2 inhibitors. 1. 4-(4-bromo2-2fluorophenylamino)-1-methylpyridin-2(1 H)-ones J. Med. Chem. 2006, 49, 441-444 (Pubitemid 43157473)
-
(2006)
Journal of Medicinal Chemistry
, vol.49
, Issue.2
, pp. 441-444
-
-
Wallace, E.M.1
Lyssikatos, J.2
Blake, J.F.3
Seo, J.4
Yang, H.W.5
Yeh, T.C.6
Perrier, M.7
Jarski, H.8
Marsh, V.9
Poch, G.10
Livingston, M.G.11
Otten, J.12
Hingorani, G.13
Woessner, R.14
Lee, P.15
Winkler, J.16
Koch, K.17
-
27
-
-
0023884412
-
Pyrazolo[3,4-b]pyridines: Syntheses, reactions, and nuclear magnetic resonance spectra
-
Lynch, B. M.; Khan, M. A.; Teo, H. C.; Pedrotti, F. Pyrazolo[3,4-b] pyridines: Syntheses, reactions, and nuclear magnetic resonance spectra Can. J. Chem. 1988, 66, 420-428
-
(1988)
Can. J. Chem.
, vol.66
, pp. 420-428
-
-
Lynch, B.M.1
Khan, M.A.2
Teo, H.C.3
Pedrotti, F.4
-
28
-
-
79956116188
-
-
WO 2009/089359.
-
Blake, J.; Gunawardana, I. W.; Le Huerou, Y.; Mohr, P. J.; Wallace, E. M.; Wang, B. Pyrazolopyridine derivatives and their pharmaceutical compositions as CHK1 and CHK2 kinase inhibitors for the treatment of various diseases and preparation thereof. WO 2009/089359.
-
Pyrazolopyridine Derivatives and Their Pharmaceutical Compositions As CHK1 and CHK2 Kinase Inhibitors for the Treatment of Various Diseases and Preparation Thereof
-
-
Blake, J.1
Gunawardana, I.W.2
Le Huerou, Y.3
Mohr, P.J.4
Wallace, E.M.5
Wang, B.6
-
29
-
-
64649100465
-
Hydroxypropyl methylcellulose acetate succinate-based spray-dried dispersions: An overview
-
Friesen, D. T.; Shanker, R.; Crew, M.; Smithey, D. T.; Curatolo, W. J.; Nightingale, J. A. S. Hydroxypropyl methylcellulose acetate succinate-based spray-dried dispersions: An overview Mol. Pharmaceutics 2008, 5, 1003-1019
-
(2008)
Mol. Pharmaceutics
, vol.5
, pp. 1003-1019
-
-
Friesen, D.T.1
Shanker, R.2
Crew, M.3
Smithey, D.T.4
Curatolo, W.J.5
Nightingale, J.A.S.6
-
30
-
-
79956099589
-
Preclinical Assessment of Novel B-RAF Inhibitors: Integrating Pharmacokinetic-Pharmacodynamic Modeling in the Drug Discovery Process
-
Details and discussion regarding the relationship between pERK inhibition and tumor response will be reported:;;;;;;;;;;;., manuscript in preparation.
-
Details and discussion regarding the relationship between pERK inhibition and tumor response will be reported: Choo, E. F.; Afflerbaugh, L.; Alicke, B.; Boggs, J.; Dinkel, D.; Gould, S.; Grina, J.; West, K.; Menghrajani, K.; Ran, Y.; Rudolph, J.; Wenglowsky, S. Preclinical Assessment of Novel B-RAF Inhibitors: Integrating Pharmacokinetic-Pharmacodynamic Modeling in the Drug Discovery Process. Xenobiotica, manuscript in preparation.
-
Xenobiotica
-
-
Choo, E.F.1
Afflerbaugh, L.2
Alicke, B.3
Boggs, J.4
Dinkel, D.5
Gould, S.6
Grina, J.7
West, K.8
Menghrajani, K.9
Ran, Y.10
Rudolph, J.11
Wenglowsky, S.12
-
31
-
-
77949685981
-
RAF inhibitors prime wild-type RAF to activate the MAPK pathway and enhance growth
-
Hatzivassiliou, G.; Song, K.; Yen, I.; Brandhuber, B. J.; Anderson, D. J.; Alvarado, R.; Ludlam, M. C.; Stokoe, D.; Gloor, S. L.; Vigers, G.; Morales, T.; Aliagas, I.; Liu, B.; Siberis, S.; Hoeflich, K. P.; Jaiswal, B. S.; Seshagiri, S.; Koeppen, H.; Belvin, M.; Friedman, L. S.; Malek, S. RAF inhibitors prime wild-type RAF to activate the MAPK pathway and enhance growth Nature 2010, 464, 431-435
-
(2010)
Nature
, vol.464
, pp. 431-435
-
-
Hatzivassiliou, G.1
Song, K.2
Yen, I.3
Brandhuber, B.J.4
Anderson, D.J.5
Alvarado, R.6
Ludlam, M.C.7
Stokoe, D.8
Gloor, S.L.9
Vigers, G.10
Morales, T.11
Aliagas, I.12
Liu, B.13
Siberis, S.14
Hoeflich, K.P.15
Jaiswal, B.S.16
Seshagiri, S.17
Koeppen, H.18
Belvin, M.19
Friedman, L.S.20
Malek, S.21
more..
-
32
-
-
74849109743
-
Kinase-dead BRAF and oncogenic RAS cooperate to drive tumor progression through CRAF
-
Heidhorn, S. J.; Milagre, C.; Whittaker, S.; Nourry, A.; Niculescu-Duvas, I.; Dhomen, N.; Hussain, J.; Reis-Filho, J.; Springer, C. J.; Pritchard, C.; Marais, R. Kinase-dead BRAF and oncogenic RAS cooperate to drive tumor progression through CRAF Cell 2010, 140, 209-221
-
(2010)
Cell
, vol.140
, pp. 209-221
-
-
Heidhorn, S.J.1
Milagre, C.2
Whittaker, S.3
Nourry, A.4
Niculescu-Duvas, I.5
Dhomen, N.6
Hussain, J.7
Reis-Filho, J.8
Springer, C.J.9
Pritchard, C.10
Marais, R.11
-
33
-
-
77949732073
-
RAF inhibitors transactivate RAF dimers and ERK signaling in cells with wild-type BRAF
-
Poulikakos, P.; Zhang, C.; Bollag, G.; Shokat, K. M.; Rosen, N. RAF inhibitors transactivate RAF dimers and ERK signaling in cells with wild-type BRAF Nature 2010, 464, 427-430
-
(2010)
Nature
, vol.464
, pp. 427-430
-
-
Poulikakos, P.1
Zhang, C.2
Bollag, G.3
Shokat, K.M.4
Rosen, N.5
-
34
-
-
77955475709
-
Selective and potent Raf inhibitors paradoxically stimulate normal cell proliferation and tumor growth
-
Carnahan, J.; Beltran, P. J.; Babij, C.; Le, Q.; Rose, M. J.; Vonderfecht, S.; Kim, J. L.; Smith, A. L.; Nagapudi, K.; Broome, M. A.; Fernando, M.; Kha, H.; Belmontes, B.; Radinsky, R.; Kendall, R.; Burgess, T. L. Selective and potent Raf inhibitors paradoxically stimulate normal cell proliferation and tumor growth Mol. Cancer Ther. 2010, 9, 2399-2410
-
(2010)
Mol. Cancer Ther.
, vol.9
, pp. 2399-2410
-
-
Carnahan, J.1
Beltran, P.J.2
Babij, C.3
Le, Q.4
Rose, M.J.5
Vonderfecht, S.6
Kim, J.L.7
Smith, A.L.8
Nagapudi, K.9
Broome, M.A.10
Fernando, M.11
Kha, H.12
Belmontes, B.13
Radinsky, R.14
Kendall, R.15
Burgess, T.L.16
|