-
1
-
-
84878942800
-
Molecular mechanisms of fibroblast growth factor signaling in physiology and pathology.
-
Belov AA and Mohammadi M. Molecular mechanisms of fibroblast growth factor signaling in physiology and pathology. Cold Spring Harb Perspect Biol. 2013; 5.
-
(2013)
Cold Spring Harb Perspect Biol.
, vol.5
-
-
Belov, A.A.1
Mohammadi, M.2
-
3
-
-
84925456768
-
Careless talk costs lives: fibroblast growth factor receptor signalling and the consequences of pathway malfunction
-
Carter EP, Fearon AE and Grose RP. Careless talk costs lives: fibroblast growth factor receptor signalling and the consequences of pathway malfunction. Trends Cell Biol. 2015; 25:221-233.
-
(2015)
Trends Cell Biol.
, vol.25
, pp. 221-233
-
-
Carter, E.P.1
Fearon, A.E.2
Grose, R.P.3
-
4
-
-
84942194341
-
Fibroblast growth factor receptor signaling in hereditary and neoplastic disease: biologic and clinical implications.
-
Helsten T, Schwaederle M and Kurzrock R. Fibroblast growth factor receptor signaling in hereditary and neoplastic disease: biologic and clinical implications. Cancer Metastasis Rev. 2015.
-
(2015)
Cancer Metastasis Rev.
-
-
Helsten, T.1
Schwaederle, M.2
Kurzrock, R.3
-
5
-
-
84859415553
-
Molecular pathways: fibroblast growth factor signaling: a new therapeutic opportunity in cancer
-
Brooks AN, Kilgour E and Smith PD. Molecular pathways: fibroblast growth factor signaling: a new therapeutic opportunity in cancer. Clin Cancer Res. 2012; 18:1855-1862.
-
(2012)
Clin Cancer Res.
, vol.18
, pp. 1855-1862
-
-
Brooks, A.N.1
Kilgour, E.2
Smith, P.D.3
-
6
-
-
84942163775
-
Targeting FGFR Signaling in Cancer
-
Touat M, Ileana E, Postel-Vinay S, Andre F and Soria JC. Targeting FGFR Signaling in Cancer. Clin Cancer Res. 2015; 21:2684-2694.
-
(2015)
Clin Cancer Res.
, vol.21
, pp. 2684-2694
-
-
Touat, M.1
Ileana, E.2
Postel-Vinay, S.3
Andre, F.4
Soria, J.C.5
-
7
-
-
79959713140
-
Fibroblast growth factors and their receptors in cancer
-
Wesche J, Haglund K and Haugsten EM. Fibroblast growth factors and their receptors in cancer. Biochem J. 2011; 437:199-213.
-
(2011)
Biochem J.
, vol.437
, pp. 199-213
-
-
Wesche, J.1
Haglund, K.2
Haugsten, E.M.3
-
8
-
-
79955667838
-
Targeting mutant fibroblast growth factor receptors in cancer
-
Greulich H and Pollock PM. Targeting mutant fibroblast growth factor receptors in cancer. Trends Mol Med. 2011; 17:283-292.
-
(2011)
Trends Mol Med.
, vol.17
, pp. 283-292
-
-
Greulich, H.1
Pollock, P.M.2
-
9
-
-
84938286765
-
Functions of Fibroblast Growth Factor Receptors in cancer defined by novel translocations and mutations
-
Gallo LH, Nelson KN, Meyer AN and Donoghue DJ. Functions of Fibroblast Growth Factor Receptors in cancer defined by novel translocations and mutations. Cytokine Growth Factor Rev. 2015; 26:425-449.
-
(2015)
Cytokine Growth Factor Rev.
, vol.26
, pp. 425-449
-
-
Gallo, L.H.1
Nelson, K.N.2
Meyer, A.N.3
Donoghue, D.J.4
-
10
-
-
84954469968
-
The FGFR Landscape in Cancer: Analysis of 4,853 Tumors by Next-Generation Sequencing
-
Helsten T, Elkin S, Arthur E, Tomson BN, Carter J and Kurzrock R. The FGFR Landscape in Cancer: Analysis of 4,853 Tumors by Next-Generation Sequencing. Clin Cancer Res. 2016; 22:259-267.
-
(2016)
Clin Cancer Res.
, vol.22
, pp. 259-267
-
-
Helsten, T.1
Elkin, S.2
Arthur, E.3
Tomson, B.N.4
Carter, J.5
Kurzrock, R.6
-
11
-
-
73549108711
-
Amplification of chromosomal segment 4q12 in non-small cell lung cancer
-
Ramos AH, Dutt A, Mermel C, Perner S, Cho J, Lafargue CJ, Johnson LA, Stiedl AC, Tanaka KE, Bass AJ, Barretina J, Weir BA, Beroukhim R, Thomas RK, Minna JD, Chirieac LR, et al. Amplification of chromosomal segment 4q12 in non-small cell lung cancer. Cancer Biol Ther. 2009; 8:2042-2050.
-
(2009)
Cancer Biol Ther.
, vol.8
, pp. 2042-2050
-
-
Ramos, A.H.1
Dutt, A.2
Mermel, C.3
Perner, S.4
Cho, J.5
Lafargue, C.J.6
Johnson, L.A.7
Stiedl, A.C.8
Tanaka, K.E.9
Bass, A.J.10
Barretina, J.11
Weir, B.A.12
Beroukhim, R.13
Thomas, R.K.14
Minna, J.D.15
Chirieac, L.R.16
-
12
-
-
0027469474
-
DNA amplification in human gastric carcinomas
-
Mor O, Ranzani GN, Ravia Y, Rotman G, Gutman M, Manor A, Amadori D, Houldsworth J, Hollstein M, Schwab M and Shiloh Y. DNA amplification in human gastric carcinomas. Cancer Genet Cytogenet. 1993; 65:111-114.
-
(1993)
Cancer Genet Cytogenet.
, vol.65
, pp. 111-114
-
-
Mor, O.1
Ranzani, G.N.2
Ravia, Y.3
Rotman, G.4
Gutman, M.5
Manor, A.6
Amadori, D.7
Houldsworth, J.8
Hollstein, M.9
Schwab, M.10
Shiloh, Y.11
-
13
-
-
34250829395
-
Frequent activating FGFR2 mutations in endometrial carcinomas parallel germline mutations associated with craniosynostosis and skeletal dysplasia syndromes
-
Pollock PM, Gartside MG, Dejeza LC, Powell MA, Mallon MA, Davies H, Mohammadi M, Futreal PA, Stratton MR, Trent JM and Goodfellow PJ. Frequent activating FGFR2 mutations in endometrial carcinomas parallel germline mutations associated with craniosynostosis and skeletal dysplasia syndromes. Oncogene. 2007; 26:7158-7162.
-
(2007)
Oncogene.
, vol.26
, pp. 7158-7162
-
-
Pollock, P.M.1
Gartside, M.G.2
Dejeza, L.C.3
Powell, M.A.4
Mallon, M.A.5
Davies, H.6
Mohammadi, M.7
Futreal, P.A.8
Stratton, M.R.9
Trent, J.M.10
Goodfellow, P.J.11
-
14
-
-
0030922231
-
Frequent translocation t(4;14) (p16.3;q32.3) in multiple myeloma is associated with increased expression and activating mutations of fibroblast growth factor receptor 3
-
Chesi M, Nardini E, Brents LA, Schrock E, Ried T, Kuehl WM and Bergsagel PL. Frequent translocation t(4;14) (p16.3;q32.3) in multiple myeloma is associated with increased expression and activating mutations of fibroblast growth factor receptor 3. Nature genetics. 1997; 16:260-264.
-
(1997)
Nature genetics.
, vol.16
, pp. 260-264
-
-
Chesi, M.1
Nardini, E.2
Brents, L.A.3
Schrock, E.4
Ried, T.5
Kuehl, W.M.6
Bergsagel, P.L.7
-
15
-
-
0032841519
-
Frequent activating mutations of FGFR3 in human bladder and cervix carcinomas
-
Cappellen D, De Oliveira C, Ricol D, de Medina S, Bourdin J, Sastre-Garau X, Chopin D, Thiery JP and Radvanyi F. Frequent activating mutations of FGFR3 in human bladder and cervix carcinomas. Nature genetics. 1999; 23:18-20.
-
(1999)
Nature genetics.
, vol.23
, pp. 18-20
-
-
Cappellen, D.1
De Oliveira, C.2
Ricol, D.3
de Medina, S.4
Bourdin, J.5
Sastre-Garau, X.6
Chopin, D.7
Thiery, J.P.8
Radvanyi, F.9
-
16
-
-
70449450426
-
Identification of FGFR4-activating mutations in human rhabdomyosarcomas that promote metastasis in xenotransplanted models
-
Taylor JGt, Cheuk AT, Tsang PS, Chung JY, Song YK, Desai K, Yu Y, Chen QR, Shah K, Youngblood V, Fang J, Kim SY, Yeung C, Helman LJ, Mendoza A, Ngo V, et al. Identification of FGFR4-activating mutations in human rhabdomyosarcomas that promote metastasis in xenotransplanted models. J Clin Invest. 2009; 119:3395-3407.
-
(2009)
J Clin Invest.
, vol.119
, pp. 3395-3407
-
-
Taylor, J.Gt.1
Cheuk, A.T.2
Tsang, P.S.3
Chung, J.Y.4
Song, Y.K.5
Desai, K.6
Yu, Y.7
Chen, Q.R.8
Shah, K.9
Youngblood, V.10
Fang, J.11
Kim, S.Y.12
Yeung, C.13
Helman, L.J.14
Mendoza, A.15
Ngo, V.16
-
17
-
-
84878781242
-
Identification of targetable FGFR gene fusions in diverse cancers
-
Wu YM, Su F, Kalyana-Sundaram S, Khazanov N, Ateeq B, Cao X, Lonigro RJ, Vats P, Wang R, Lin SF, Cheng AJ, Kunju LP, Siddiqui J, Tomlins SA, Wyngaard P, Sadis S, et al. Identification of targetable FGFR gene fusions in diverse cancers. Cancer Discov. 2013; 3:636-647.
-
(2013)
Cancer Discov.
, vol.3
, pp. 636-647
-
-
Wu, Y.M.1
Su, F.2
Kalyana-Sundaram, S.3
Khazanov, N.4
Ateeq, B.5
Cao, X.6
Lonigro, R.J.7
Vats, P.8
Wang, R.9
Lin, S.F.10
Cheng, A.J.11
Kunju, L.P.12
Siddiqui, J.13
Tomlins, S.A.14
Wyngaard, P.15
Sadis, S.16
-
18
-
-
84860120185
-
AZD4547: an orally bioavailable, potent, and selective inhibitor of the fibroblast growth factor receptor tyrosine kinase family
-
Gavine PR, Mooney L, Kilgour E, Thomas AP, Al-Kadhimi K, Beck S, Rooney C, Coleman T, Baker D, Mellor MJ, Brooks AN and Klinowska T. AZD4547: an orally bioavailable, potent, and selective inhibitor of the fibroblast growth factor receptor tyrosine kinase family. Cancer Res. 2012; 72:2045-2056.
-
(2012)
Cancer Res.
, vol.72
, pp. 2045-2056
-
-
Gavine, P.R.1
Mooney, L.2
Kilgour, E.3
Thomas, A.P.4
Al-Kadhimi, K.5
Beck, S.6
Rooney, C.7
Coleman, T.8
Baker, D.9
Mellor, M.J.10
Brooks, A.N.11
Klinowska, T.12
-
19
-
-
80054900437
-
Discovery of 3-(2,6-dichloro-3,5-dimethoxy-phenyl)-1-(6-[4-(4-ethyl-piperazin-1-yl)-phenylamin o]-pyrimidin-4-yl)-1-methyl-urea (NVPBGJ398), a potent and selective inhibitor of the fibroblast growth factor receptor family of receptor tyrosine kinase
-
Guagnano V, Furet P, Spanka C, Bordas V, Le Douget M, Stamm C, Brueggen J, Jensen MR, Schnell C, Schmid H, Wartmann M, Berghausen J, Drueckes P, Zimmerlin A, Bussiere D, Murray J, et al. Discovery of 3-(2,6-dichloro-3,5-dimethoxy-phenyl)-1-(6-[4-(4-ethyl-piperazin-1-yl)-phenylamin o]-pyrimidin-4-yl)-1-methyl-urea (NVPBGJ398), a potent and selective inhibitor of the fibroblast growth factor receptor family of receptor tyrosine kinase. J Med Chem. 2011; 54:7066-7083.
-
(2011)
J Med Chem.
, vol.54
, pp. 7066-7083
-
-
Guagnano, V.1
Furet, P.2
Spanka, C.3
Bordas, V.4
Le Douget, M.5
Stamm, C.6
Brueggen, J.7
Jensen, M.R.8
Schnell, C.9
Schmid, H.10
Wartmann, M.11
Berghausen, J.12
Drueckes, P.13
Zimmerlin, A.14
Bussiere, D.15
Murray, J.16
-
20
-
-
84966675289
-
JNJ-42756493 is a potent and selective FGFR1-4 kinase inhibitor with promise for clinical use in patients with FGFR driven tumors.
-
Presented at the 15th World Conference on Lung Cancer, Sydney, Australia, October 27-31
-
Perera T, Jovcheva E, Vialard J and al e. JNJ-42756493 is a potent and selective FGFR1-4 kinase inhibitor with promise for clinical use in patients with FGFR driven tumors. Presented at the 15th World Conference on Lung Cancer, Sydney, Australia, October 27-31. 2013.
-
(2013)
-
-
Perera, T.1
Jovcheva, E.2
Vialard, J.3
-
21
-
-
71349085679
-
Mutant fibroblast growth factor receptor 3 induces intracellular signaling and cellular transformation in a cell type-and mutation-specific manner
-
di Martino E, L'Hote CG, Kennedy W, Tomlinson DC and Knowles MA. Mutant fibroblast growth factor receptor 3 induces intracellular signaling and cellular transformation in a cell type-and mutation-specific manner. Oncogene. 2009; 28:4306-4316.
-
(2009)
Oncogene.
, vol.28
, pp. 4306-4316
-
-
di Martino, E.1
L'Hote, C.G.2
Kennedy, W.3
Tomlinson, D.C.4
Knowles, M.A.5
-
22
-
-
84879417823
-
Tumour cell responses to new fibroblast growth factor receptor tyrosine kinase inhibitors and identification of a gatekeeper mutation in FGFR3 as a mechanism of acquired resistance
-
Chell V, Balmanno K, Little AS, Wilson M, Andrews S, Blockley L, Hampson M, Gavine PR and Cook SJ. Tumour cell responses to new fibroblast growth factor receptor tyrosine kinase inhibitors and identification of a gatekeeper mutation in FGFR3 as a mechanism of acquired resistance. Oncogene. 2013; 32:3059-3070.
-
(2013)
Oncogene.
, vol.32
, pp. 3059-3070
-
-
Chell, V.1
Balmanno, K.2
Little, A.S.3
Wilson, M.4
Andrews, S.5
Blockley, L.6
Hampson, M.7
Gavine, P.R8
Cook, S.J.9
-
23
-
-
84885432815
-
Structural mimicry of a-loop tyrosine phosphorylation by a pathogenic FGF receptor 3 mutation
-
Huang Z, Chen H, Blais S, Neubert TA, Li X and Mohammadi M. Structural mimicry of a-loop tyrosine phosphorylation by a pathogenic FGF receptor 3 mutation. Structure. 2013; 21:1889-1896.
-
(2013)
Structure.
, vol.21
, pp. 1889-1896
-
-
Huang, Z.1
Chen, H.2
Blais, S.3
Neubert, T.A.4
Li, X.5
Mohammadi, M.6
-
24
-
-
17844402791
-
Bad bones, absent smell, selfish testes: the pleiotropic consequences of human FGF receptor mutations
-
Wilkie AO. Bad bones, absent smell, selfish testes: the pleiotropic consequences of human FGF receptor mutations. Cytokine Growth Factor Rev. 2005; 16:187-203.
-
(2005)
Cytokine Growth Factor Rev.
, vol.16
, pp. 187-203
-
-
Wilkie, A.O.1
-
25
-
-
84875421249
-
Exploring mechanisms of FGF signalling through the lens of structural biology
-
Goetz R and Mohammadi M. Exploring mechanisms of FGF signalling through the lens of structural biology. Nat Rev Mol Cell Biol. 2013; 14:166-180.
-
(2013)
Nat Rev Mol Cell Biol.
, vol.14
, pp. 166-180
-
-
Goetz, R.1
Mohammadi, M.2
-
26
-
-
84881396090
-
Computational approaches to identify functional genetic variants in cancer genomes
-
Gonzalez-Perez A, Mustonen V, Reva B, Ritchie GR, Creixell P, Karchin R, Vazquez M, Fink JL, Kassahn KS, Pearson JV, Bader GD, Boutros PC, Muthuswamy L, Ouellette BF, Reimand J, Linding R, et al. Computational approaches to identify functional genetic variants in cancer genomes. Nat Methods. 2013; 10:723-729.
-
(2013)
Nat Methods.
, vol.10
, pp. 723-729
-
-
Gonzalez-Perez, A.1
Mustonen, V.2
Reva, B.3
Ritchie, G.R.4
Creixell, P.5
Karchin, R.6
Vazquez, M.7
Fink, J.L.8
Kassahn, K.S.9
Pearson, J.V.10
Bader, G.D.11
Boutros, P.C.12
Muthuswamy, L.13
Ouellette, B.F.14
Reimand, J.15
Linding, R.16
-
27
-
-
84991233923
-
Benchmarking mutation effect prediction algorithms using functionally validated cancer-related missense mutations
-
Martelotto LG, Ng CK, De Filippo MR, Zhang Y, Piscuoglio S, Lim RS, Shen R, Norton L, Reis-Filho JS and Weigelt B. Benchmarking mutation effect prediction algorithms using functionally validated cancer-related missense mutations. Genome Biol. 2014; 15:484.
-
(2014)
Genome Biol.
, vol.15
, pp. 484
-
-
Martelotto, L.G.1
Ng, C.K.2
De Filippo, M.R.3
Zhang, Y.4
Piscuoglio, S.5
Lim, R.S.6
Shen, R.7
Norton, L.8
Reis-Filho, J.S.9
Weigelt, B.10
-
28
-
-
79953715693
-
Improving the assessment of the outcome of nonsynonymous SNVs with a consensus deleteriousness score, Condel
-
Gonzalez-Perez A and Lopez-Bigas N. Improving the assessment of the outcome of nonsynonymous SNVs with a consensus deleteriousness score, Condel. Am J Hum Genet. 2011; 88:440-449.
-
(2011)
Am J Hum Genet.
, vol.88
, pp. 440-449
-
-
Gonzalez-Perez, A.1
Lopez-Bigas, N.2
-
29
-
-
23144436398
-
The FoldX web server: an online force field
-
Schymkowitz J, Borg J, Stricher F, Nys R, Rousseau F and Serrano L. The FoldX web server: an online force field. Nucleic Acids Res. 2005; 33:W382-388.
-
(2005)
Nucleic Acids Res.
, vol.33
, pp. W382-388
-
-
Schymkowitz, J.1
Borg, J.2
Stricher, F.3
Nys, R.4
Rousseau, F.5
Serrano, L.6
-
30
-
-
77953679934
-
The precise sequence of FGF receptor autophosphorylation is kinetically driven and is disrupted by oncogenic mutations
-
Lew ED, Furdui CM, Anderson KS and Schlessinger J. The precise sequence of FGF receptor autophosphorylation is kinetically driven and is disrupted by oncogenic mutations. Sci Signal. 2009; 2:ra6.
-
(2009)
Sci Signal.
, vol.2
, pp. ra6
-
-
Lew, E.D.1
Furdui, C.M.2
Anderson, K.S.3
Schlessinger, J.4
-
31
-
-
84880806523
-
Cracking the molecular origin of intrinsic tyrosine kinase activity through analysis of pathogenic gain-of-function mutations
-
Chen H, Huang Z, Dutta K, Blais S, Neubert TA, Li X, Cowburn D, Traaseth NJ and Mohammadi M. Cracking the molecular origin of intrinsic tyrosine kinase activity through analysis of pathogenic gain-of-function mutations. Cell Rep. 2013; 4:376-384.
-
(2013)
Cell Rep.
, vol.4
, pp. 376-384
-
-
Chen, H.1
Huang, Z.2
Dutta, K.3
Blais, S.4
Neubert, T.A.5
Li, X.6
Cowburn, D.7
Traaseth, N.J.8
Mohammadi, M.9
-
32
-
-
0029032394
-
A recurrent mutation in the tyrosine kinase domain of fibroblast growth factor receptor 3 causes hypochondroplasia
-
Bellus GA, McIntosh I, Smith EA, Aylsworth AS, Kaitila I, Horton WA, Greenhaw GA, Hecht JT and Francomano CA. A recurrent mutation in the tyrosine kinase domain of fibroblast growth factor receptor 3 causes hypochondroplasia. Nature genetics. 1995; 10:357-359.
-
(1995)
Nature genetics.
, vol.10
, pp. 357-359
-
-
Bellus, G.A.1
McIntosh, I.2
Smith, E.A.3
Aylsworth, A.S.4
Kaitila, I.5
Horton, W.A.6
Greenhaw, G.A.7
Hecht, J.T.8
Francomano, C.A.9
-
33
-
-
0029945085
-
Profound ligand-independent kinase activation of fibroblast growth factor receptor 3 by the activation loop mutation responsible for a lethal skeletal dysplasia, thanatophoric dysplasia type II
-
Webster MK, D'Avis PY, Robertson SC and Donoghue DJ. Profound ligand-independent kinase activation of fibroblast growth factor receptor 3 by the activation loop mutation responsible for a lethal skeletal dysplasia, thanatophoric dysplasia type II. Molecular and cellular biology. 1996; 16:4081-4087.
-
(1996)
Molecular and cellular biology.
, vol.16
, pp. 4081-4087
-
-
Webster, M.K.1
D'Avis, P.Y.2
Robertson, S.C.3
Donoghue, D.J.4
-
34
-
-
0029935895
-
Graded activation of fibroblast growth factor receptor 3 by mutations causing achondroplasia and thanatophoric dysplasia
-
Naski MC, Wang Q, Xu J and Ornitz DM. Graded activation of fibroblast growth factor receptor 3 by mutations causing achondroplasia and thanatophoric dysplasia. Nature genetics. 1996; 13:233-237.
-
(1996)
Nature genetics.
, vol.13
, pp. 233-237
-
-
Naski, M.C.1
Wang, Q.2
Xu, J.3
Ornitz, D.M.4
-
35
-
-
53549104402
-
Activation of tyrosine kinases by mutation of the gatekeeper threonine
-
Azam M, Seeliger MA, Gray NS, Kuriyan J and Daley GQ. Activation of tyrosine kinases by mutation of the gatekeeper threonine. Nat Struct Mol Biol. 2008; 15:1109-1118.
-
(2008)
Nat Struct Mol Biol.
, vol.15
, pp. 1109-1118
-
-
Azam, M.1
Seeliger, M.A.2
Gray, N.S.3
Kuriyan, J.4
Daley, G.Q.5
-
36
-
-
40049099220
-
The T790M mutation in EGFR kinase causes drug resistance by increasing the affinity for ATP
-
Yun CH, Mengwasser KE, Toms AV, Woo MS, Greulich H, Wong KK, Meyerson M and Eck MJ. The T790M mutation in EGFR kinase causes drug resistance by increasing the affinity for ATP. Proc Natl Acad Sci U S A. 2008; 105:2070-2075.
-
(2008)
Proc Natl Acad Sci U S A.
, vol.105
, pp. 2070-2075
-
-
Yun, C.H.1
Mengwasser, K.E.2
Toms, A.V.3
Woo, M.S.4
Greulich, H.5
Wong, K.K.6
Meyerson, M.7
Eck, M.J.8
-
37
-
-
84928731157
-
The Effect of Mutations on Drug Sensitivity and Kinase Activity of Fibroblast Growth Factor Receptors: A Combined Experimental and Theoretical Study
-
Bunney TD, Wan S, Thiyagarajan N, Sutto L, Williams SV, Ashford P, Koss H, Knowles MA, Gervasio FL, Coveney PV and Katan M. The Effect of Mutations on Drug Sensitivity and Kinase Activity of Fibroblast Growth Factor Receptors: A Combined Experimental and Theoretical Study. EBioMedicine. 2015; 2:194-204.
-
(2015)
EBioMedicine.
, vol.2
, pp. 194-204
-
-
Bunney, T.D.1
Wan, S.2
Thiyagarajan, N.3
Sutto, L.4
Williams, S.V.5
Ashford, P.6
Koss, H.7
Knowles, M.A.8
Gervasio, F.L.9
Coveney, P.V.10
Katan, M.11
-
38
-
-
33947101019
-
Patterns of somatic mutation in human cancer genomes
-
Greenman C, Stephens P, Smith R, Dalgliesh GL, Hunter C, Bignell G, Davies H, Teague J, Butler A, Stevens C, Edkins S, O'Meara S, Vastrik I, Schmidt EE, Avis T, Barthorpe S, et al. Patterns of somatic mutation in human cancer genomes. Nature. 2007; 446:153-158.
-
(2007)
Nature.
, vol.446
, pp. 153-158
-
-
Greenman, C.1
Stephens, P.2
Smith, R.3
Dalgliesh, G.L.4
Hunter, C.5
Bignell, G.6
Davies, H.7
Teague, J.8
Butler, A.9
Stevens, C.10
Edkins, S.11
O'Meara, S.12
Vastrik, I.13
Schmidt, E.E.14
Avis, T.15
Barthorpe, S.16
-
39
-
-
84922056687
-
ProKinO: a unified resource for mining the cancer kinome
-
McSkimming DI, Dastgheib S, Talevich E, Narayanan A, Katiyar S, Taylor SS, Kochut K and Kannan N. ProKinO: a unified resource for mining the cancer kinome. Hum Mutat. 2015; 36:175-186.
-
(2015)
Hum Mutat.
, vol.36
, pp. 175-186
-
-
McSkimming, D.I.1
Dastgheib, S.2
Talevich, E.3
Narayanan, A.4
Katiyar, S.5
Taylor, S.S.6
Kochut, K.7
Kannan, N.8
-
40
-
-
75149170979
-
Fibroblast growth factor signalling: from development to cancer
-
Turner N and Grose R. Fibroblast growth factor signalling: from development to cancer. Nat Rev Cancer. 2010; 10:116-129.
-
(2010)
Nat Rev Cancer.
, vol.10
, pp. 116-129
-
-
Turner, N.1
Grose, R.2
-
41
-
-
34548250374
-
A molecular brake in the kinase hinge region regulates the activity of receptor tyrosine kinases
-
Chen H, Ma J, Li W, Eliseenkova AV, Xu C, Neubert TA, Miller WT and Mohammadi M. A molecular brake in the kinase hinge region regulates the activity of receptor tyrosine kinases. Mol Cell. 2007; 27:717-730.
-
(2007)
Mol Cell.
, vol.27
, pp. 717-730
-
-
Chen, H.1
Ma, J.2
Li, W.3
Eliseenkova, A.V.4
Xu, C.5
Neubert, T.A.6
Miller, W.T.7
Mohammadi, M.8
-
42
-
-
84871491773
-
FGFR genetic alterations predict for sensitivity to NVPBGJ398, a selective pan-FGFR inhibitor
-
Guagnano V, Kauffmann A, Wohrle S, Stamm C, Ito M, Barys L, Pornon A, Yao Y, Li F, Zhang Y, Chen Z, Wilson CJ, Bordas V, Le Douget M, Gaither LA, Borawski J, et al. FGFR genetic alterations predict for sensitivity to NVPBGJ398, a selective pan-FGFR inhibitor. Cancer Discov. 2012; 2:1118-1133.
-
(2012)
Cancer Discov.
, vol.2
, pp. 1118-1133
-
-
Guagnano, V.1
Kauffmann, A.2
Wohrle, S.3
Stamm, C.4
Ito, M.5
Barys, L.6
Pornon, A.7
Yao, Y.8
Li, F.9
Zhang, Y.10
Chen, Z.11
Wilson, C.J.12
Bordas, V.13
Le Douget, M.14
Gaither, L.A.15
Borawski, J.16
-
43
-
-
84914094459
-
Structural insights into FGFR kinase isoform selectivity: diverse binding modes of AZD4547 and ponatinib in complex with FGFR1 and FGFR4
-
Tucker JA, Klein T, Breed J, Breeze AL, Overman R, Phillips C and Norman RA. Structural insights into FGFR kinase isoform selectivity: diverse binding modes of AZD4547 and ponatinib in complex with FGFR1 and FGFR4. Structure. 2014; 22:1764-1774.
-
(2014)
Structure.
, vol.22
, pp. 1764-1774
-
-
Tucker, J.A.1
Klein, T.2
Breed, J.3
Breeze, A.L.4
Overman, R.5
Phillips, C.6
Norman, R.A.7
-
44
-
-
84945186800
-
Phase I Dose-Escalation Study of JNJ-42756493, an Oral Pan-Fibroblast Growth Factor Receptor Inhibitor, in Patients With Advanced Solid Tumors
-
Tabernero J, Bahleda R, Dienstmann R, Infante JR, Mita A, Italiano A, Calvo E, Moreno V, Adamo B, Gazzah A, Zhong B, Platero SJ, Smit JW, Stuyckens K, Chatterjee-Kishore M, Rodon J, et al. Phase I Dose-Escalation Study of JNJ-42756493, an Oral Pan-Fibroblast Growth Factor Receptor Inhibitor, in Patients With Advanced Solid Tumors. J Clin Oncol. 2015; 33:3401-3408.
-
(2015)
J Clin Oncol.
, vol.33
, pp. 3401-3408
-
-
Tabernero, J.1
Bahleda, R.2
Dienstmann, R.3
Infante, J.R.4
Mita, A.5
Italiano, A.6
Calvo, E.7
Moreno, V.8
Adamo, B.9
Gazzah, A.10
Zhong, B.11
Platero, S.J.12
Smit, J.W.13
Stuyckens, K.14
Chatterjee-Kishore, M.15
Rodon, J.16
-
45
-
-
84862285959
-
Protein-ligand crystal structures can guide the design of selective inhibitors of the FGFR tyrosine kinase
-
Norman RA, Schott AK, Andrews DM, Breed J, Foote KM, Garner AP, Ogg D, Orme JP, Pink JH, Roberts K, Rudge DA, Thomas AP and Leach AG. Protein-ligand crystal structures can guide the design of selective inhibitors of the FGFR tyrosine kinase. J Med Chem. 2012; 55:5003-5012.
-
(2012)
J Med Chem.
, vol.55
, pp. 5003-5012
-
-
Norman, R.A.1
Schott, A.K.2
Andrews, D.M.3
Breed, J.4
Foote, K.M.5
Garner, A.P.6
Ogg, D.7
Orme, J.P.8
Pink, J.H.9
Roberts, K.10
Rudge, D.A.11
Thomas, A.P.12
Leach, A.G.13
-
46
-
-
84881039897
-
The N550K/H mutations in FGFR2 confer differential resistance to PD173074, dovitinib, and ponatinib ATP-competitive inhibitors
-
Byron SA, Chen H, Wortmann A, Loch D, Gartside MG, Dehkhoda F, Blais SP, Neubert TA, Mohammadi M and Pollock PM. The N550K/H mutations in FGFR2 confer differential resistance to PD173074, dovitinib, and ponatinib ATP-competitive inhibitors. Neoplasia. 2013; 15:975-988.
-
(2013)
Neoplasia.
, vol.15
, pp. 975-988
-
-
Byron, S.A.1
Chen, H.2
Wortmann, A.3
Loch, D.4
Gartside, M.G.5
Dehkhoda, F.6
Blais, S.P.7
Neubert, T.A.8
Mohammadi, M.9
Pollock, P.M.10
-
47
-
-
70350507997
-
AP24534, a pan-BCR-ABL inhibitor for chronic myeloid leukemia, potently inhibits the T315I mutant and overcomes mutation-based resistance
-
O'Hare T, Shakespeare WC, Zhu X, Eide CA, Rivera VM, Wang F, Adrian LT, Zhou T, Huang WS, Xu Q, Metcalf CA, 3rd, Tyner JW, Loriaux MM, Corbin AS, Wardwell S, Ning Y, et al. AP24534, a pan-BCR-ABL inhibitor for chronic myeloid leukemia, potently inhibits the T315I mutant and overcomes mutation-based resistance. Cancer Cell. 2009; 16:401-412.
-
(2009)
Cancer Cell.
, vol.16
, pp. 401-412
-
-
O'Hare, T.1
Shakespeare, W.C.2
Zhu, X.3
Eide, C.A.4
Rivera, V.M.5
Wang, F.6
Adrian, L.T.7
Zhou, T.8
Huang, W.S.9
Xu, Q.10
Metcalf, C.A.11
Tyner, J.W.12
Loriaux, M.M.13
Corbin, A.S.14
Wardwell, S.15
Ning, Y.16
-
48
-
-
84937944992
-
Structural and dynamic insights into the energetics of activation loop rearrangement in FGFR1 kinase
-
Klein T, Vajpai N, Phillips JJ, Davies G, Holdgate GA, Phillips C, Tucker JA, Norman RA, Scott AD, Higazi DR, Lowe D, Thompson GS and Breeze AL. Structural and dynamic insights into the energetics of activation loop rearrangement in FGFR1 kinase. Nat Commun. 2015; 6:7877.
-
(2015)
Nat Commun.
, vol.6
, pp. 7877
-
-
Klein, T.1
Vajpai, N.2
Phillips, J.J.3
Davies, G.4
Holdgate, G.A.5
Phillips, C.6
Tucker, J.A.7
Norman, R.A.8
Scott, A.D.9
Higazi, D.R.10
Lowe, D.11
Thompson, G.S.12
Breeze, A.L.13
-
50
-
-
24344468707
-
Constitutive activating mutation of the FGFR3b in oral squamous cell carcinomas
-
Zhang Y, Hiraishi Y, Wang H, Sumi KS, Hayashido Y, Toratani S, Kan M, Sato JD and Okamoto T. Constitutive activating mutation of the FGFR3b in oral squamous cell carcinomas. Int J Cancer. 2005; 117:166-168.
-
(2005)
Int J Cancer.
, vol.117
, pp. 166-168
-
-
Zhang, Y.1
Hiraishi, Y.2
Wang, H.3
Sumi, K.S.4
Hayashido, Y.5
Toratani, S.6
Kan, M.7
Sato, J.D.8
Okamoto, T.9
-
51
-
-
33947257482
-
Analysis of fibroblast growth factor receptor 3 G697C mutation in oral squamous cell carcinomas
-
author reply 2060
-
Aubertin J, Tourpin S, Janot F, Ahomadegbe JC and Radvanyi F. Analysis of fibroblast growth factor receptor 3 G697C mutation in oral squamous cell carcinomas. Int J Cancer. 2007; 120:2058-2059; author reply 2060.
-
(2007)
Int J Cancer.
, vol.120
, pp. 2058-2059
-
-
Aubertin, J.1
Tourpin, S.2
Janot, F.3
Ahomadegbe, J.C.4
Radvanyi, F.5
-
52
-
-
0033659625
-
Distinct missense mutations of the FGFR3 lys650 codon modulate receptor kinase activation and the severity of the skeletal dysplasia phenotype
-
Bellus GA, Spector EB, Speiser PW, Weaver CA, Garber AT, Bryke CR, Israel J, Rosengren SS, Webster MK, Donoghue DJ and Francomano CA. Distinct missense mutations of the FGFR3 lys650 codon modulate receptor kinase activation and the severity of the skeletal dysplasia phenotype. Am J Hum Genet. 2000; 67:1411-1421.
-
(2000)
Am J Hum Genet.
, vol.67
, pp. 1411-1421
-
-
Bellus, G.A.1
Spector, E.B.2
Speiser, P.W.3
Weaver, C.A.4
Garber, A.T.5
Bryke, C.R.6
Israel, J.7
Rosengren, S.S.8
Webster, M.K.9
Donoghue, D.J.10
Francomano, C.A.11
-
53
-
-
78650875209
-
Small molecule FGF receptor inhibitors block FGFR-dependent urothelial carcinoma growth in vitro and in vivo
-
Lamont FR, Tomlinson DC, Cooper PA, Shnyder SD, Chester JD and Knowles MA. Small molecule FGF receptor inhibitors block FGFR-dependent urothelial carcinoma growth in vitro and in vivo. Br J Cancer. 2011; 104:75-82.
-
(2011)
Br J Cancer.
, vol.104
, pp. 75-82
-
-
Lamont, F.R.1
Tomlinson, D.C.2
Cooper, P.A.3
Shnyder, S.D.4
Chester, J.D.5
Knowles, M.A.6
-
54
-
-
84871217393
-
Translating the therapeutic potential of AZD4547 in FGFR1-amplified non-small cell lung cancer through the use of patient-derived tumor xenograft models
-
Zhang J, Zhang L, Su X, Li M, Xie L, Malchers F, Fan S, Yin X, Xu Y, Liu K, Dong Z, Zhu G, Qian Z, Tang L, Schottle J, Zhan P, et al. Translating the therapeutic potential of AZD4547 in FGFR1-amplified non-small cell lung cancer through the use of patient-derived tumor xenograft models. Clin Cancer Res. 2012; 18:6658-6667.
-
(2012)
Clin Cancer Res.
, vol.18
, pp. 6658-6667
-
-
Zhang, J.1
Zhang, L.2
Su, X.3
Li, M.4
Xie, L.5
Malchers, F.6
Fan, S.7
Yin, X.8
Xu, Y.9
Liu, K.10
Dong, Z.11
Zhu, G.12
Qian, Z.13
Tang, L.14
Schottle, J.15
Zhan, P.16
-
55
-
-
84877100340
-
FGFR2 gene amplification in gastric cancer predicts sensitivity to the selective FGFR inhibitor AZD4547
-
Xie L, Su X, Zhang L, Yin X, Tang L, Zhang X, Xu Y, Gao Z, Liu K, Zhou M, Gao B, Shen D, Zhang L, Ji J, Gavine PR, Zhang J, et al. FGFR2 gene amplification in gastric cancer predicts sensitivity to the selective FGFR inhibitor AZD4547. Clin Cancer Res. 2013; 19:2572-2583.
-
(2013)
Clin Cancer Res.
, vol.19
, pp. 2572-2583
-
-
Xie, L.1
Su, X.2
Zhang, L.3
Yin, X.4
Tang, L.5
Zhang, X.6
Xu, Y.7
Gao, Z.8
Liu, K.9
Zhou, M.10
Gao, B.11
Shen, D.12
Zhang, L.13
Ji, J.14
Gavine, P.R.15
Zhang, J.16
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