-
1
-
-
84879859652
-
Targeting FGFR with dovitinib (TKI258): preclinical and clinical data in breast cancer
-
Andre F., Bachelot T., Campone M., Dalenc F., Perez-Garcia J.M., Hurvitz S.A., Turner N., Rugo H., Smith J.W., Deudon S., Shi M., Zhang Y., Kay A., Porta D.G., Yovine A., Baselga J. Targeting FGFR with dovitinib (TKI258): preclinical and clinical data in breast cancer. Clin. Cancer Res. 2013, 19:3693-3702.
-
(2013)
Clin. Cancer Res.
, vol.19
, pp. 3693-3702
-
-
Andre, F.1
Bachelot, T.2
Campone, M.3
Dalenc, F.4
Perez-Garcia, J.M.5
Hurvitz, S.A.6
Turner, N.7
Rugo, H.8
Smith, J.W.9
Deudon, S.10
Shi, M.11
Zhang, Y.12
Kay, A.13
Porta, D.G.14
Yovine, A.15
Baselga, J.16
-
2
-
-
84923829774
-
Novel mutations in neuroendocrine carcinoma of the breast: possible therapeutic targets
-
Ang D., Ballard M., Beadling C., Warrick A., Schilling A., O'Gara R., Pukay M., Neff T.L., West R.B., Corless C.L., Troxell M.L. Novel mutations in neuroendocrine carcinoma of the breast: possible therapeutic targets. Diagn. Mol. Pathol. 2015, 23:97-103.
-
(2015)
Diagn. Mol. Pathol.
, vol.23
, pp. 97-103
-
-
Ang, D.1
Ballard, M.2
Beadling, C.3
Warrick, A.4
Schilling, A.5
O'Gara, R.6
Pukay, M.7
Neff, T.L.8
West, R.B.9
Corless, C.L.10
Troxell, M.L.11
-
3
-
-
33646259689
-
Anticipating clinical resistance to target-directed agents: the BCR-ABL paradigm
-
Azam M., Daley G.Q. Anticipating clinical resistance to target-directed agents: the BCR-ABL paradigm. Mol. Diagn. Ther. 2006, 10:67-76.
-
(2006)
Mol. Diagn. Ther.
, vol.10
, pp. 67-76
-
-
Azam, M.1
Daley, G.Q.2
-
4
-
-
53549104402
-
Activation of tyrosine kinases by mutation of the gatekeeper threonine
-
Azam M., Seeliger M.A., Gray N.S., Kuriyan J., Daley G.Q. 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
-
5
-
-
77649251478
-
Asymmetric receptor contact is required for tyrosine autophosphorylation of fibroblast growth factor receptor in living cells
-
Bae J.H., Boggon T.J., Tome F., Mandiyan V., Lax I., Schlessinger J. Asymmetric receptor contact is required for tyrosine autophosphorylation of fibroblast growth factor receptor in living cells. Proc. Natl. Acad. Sci. U. S. A. 2010, 107:2866-2871.
-
(2010)
Proc. Natl. Acad. Sci. U. S. A.
, vol.107
, pp. 2866-2871
-
-
Bae, J.H.1
Boggon, T.J.2
Tome, F.3
Mandiyan, V.4
Lax, I.5
Schlessinger, J.6
-
6
-
-
61649100307
-
The FGF family: biology, pathophysiology and therapy
-
Beenken A., Mohammadi M. The FGF family: biology, pathophysiology and therapy. Nat. Rev. Drug Discov. 2009, 8:235-253.
-
(2009)
Nat. Rev. Drug Discov.
, vol.8
, pp. 235-253
-
-
Beenken, A.1
Mohammadi, M.2
-
7
-
-
84859415553
-
Molecular pathways: fibroblast growth factor signaling: a new therapeutic opportunity in cancer
-
Brooks A.N., Kilgour E., Smith P.D. 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
-
8
-
-
33750040264
-
Free-energy landscape for beta hairpin folding from combined parallel tempering and metadynamics
-
Bussi G., Gervasio F.L., Laio A., Parrinello M. Free-energy landscape for beta hairpin folding from combined parallel tempering and metadynamics. J. Am. Chem. Soc. 2006, 128:13435-13441.
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 13435-13441
-
-
Bussi, G.1
Gervasio, F.L.2
Laio, A.3
Parrinello, M.4
-
9
-
-
84881039897
-
The N550K/H mutations in FGFR2 confer differential resistance to PD173074, dovitinib, and ponatinib ATP-competitive inhibitors
-
Byron S.A., Chen H., Wortmann A., Loch D., Gartside M.G., Dehkhoda F., Blais S.P., Neubert T.A., Mohammadi M., Pollock P.M. 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
-
10
-
-
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 A.S., Wilson M., Andrews S., Blockley L., Hampson M., Gavine P.R., Cook S.J. 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.R.8
Cook, S.J.9
-
11
-
-
77955367484
-
A type-II kinase inhibitor capable of inhibiting the T315I "gatekeeper" mutant of Bcr-Abl
-
Choi H.G., Ren P., Adrian F., Sun F., Lee H.S., Wang X., Ding Q., Zhang G., Xie Y., Zhang J., Liu Y., Tuntland T., Warmuth M., Manley P.W., Mestan J., Gray N.S., Sim T. A type-II kinase inhibitor capable of inhibiting the T315I "gatekeeper" mutant of Bcr-Abl. J. Med. Chem. 2010, 53:5439-5448.
-
(2010)
J. Med. Chem.
, vol.53
, pp. 5439-5448
-
-
Choi, H.G.1
Ren, P.2
Adrian, F.3
Sun, F.4
Lee, H.S.5
Wang, X.6
Ding, Q.7
Zhang, G.8
Xie, Y.9
Zhang, J.10
Liu, Y.11
Tuntland, T.12
Warmuth, M.13
Manley, P.W.14
Mestan, J.15
Gray, N.S.16
Sim, T.17
-
12
-
-
78049426513
-
EML4-ALK mutations in lung cancer that confer resistance to ALK inhibitors
-
Choi Y.L., Soda M., Yamashita Y., Ueno T., Takashima J., Nakajima T., Yatabe Y., Takeuchi K., Hamada T., Haruta H., Ishikawa Y., Kimura H., Mitsudomi T., Tanio Y., Mano H., Group, A.L.K.L.C. EML4-ALK mutations in lung cancer that confer resistance to ALK inhibitors. N. Engl. J. Med. 2010, 363:1734-1739.
-
(2010)
N. Engl. J. Med.
, vol.363
, pp. 1734-1739
-
-
Choi, Y.L.1
Soda, M.2
Yamashita, Y.3
Ueno, T.4
Takashima, J.5
Nakajima, T.6
Yatabe, Y.7
Takeuchi, K.8
Hamada, T.9
Haruta, H.10
Ishikawa, Y.11
Kimura, H.12
Mitsudomi, T.13
Tanio, Y.14
Mano, H.15
-
13
-
-
0344987881
-
A tyrosine kinase created by fusion of the PDGFRA and FIP1L1 genes as a therapeutic target of imatinib in idiopathic hypereosinophilic syndrome
-
Cools J., Deangelo D.J., Gotlib J., Stover E.H., Legare R.D., Cortes J., Kutok J., Clark J., Galinsky I., Griffin J.D., Cross N.C., Tefferi A., Malone J., Alam R., Schrier S.L., Schmid J., Rose M., Vandenberghe P., Verhoef G., Boogaerts M., Wlodarska I., Kantarjian H., Marynen P., Coutre S.E., Stone R., Gilliland D.G. A tyrosine kinase created by fusion of the PDGFRA and FIP1L1 genes as a therapeutic target of imatinib in idiopathic hypereosinophilic syndrome. N. Engl. J. Med. 2003, 348:1201-1214.
-
(2003)
N. Engl. J. Med.
, vol.348
, pp. 1201-1214
-
-
Cools, J.1
Deangelo, D.J.2
Gotlib, J.3
Stover, E.H.4
Legare, R.D.5
Cortes, J.6
Kutok, J.7
Clark, J.8
Galinsky, I.9
Griffin, J.D.10
Cross, N.C.11
Tefferi, A.12
Malone, J.13
Alam, R.14
Schrier, S.L.15
Schmid, J.16
Rose, M.17
Vandenberghe, P.18
Verhoef, G.19
Boogaerts, M.20
Wlodarska, I.21
Kantarjian, H.22
Marynen, P.23
Coutre, S.E.24
Stone, R.25
Gilliland, D.G.26
more..
-
14
-
-
84919443958
-
Patient-derived models of acquired resistance can identify effective drug combinations for cancer
-
Crystal A.S., Shaw A.T., Sequist L.V., Friboulet L., Niederst M.J., Lockerman E.L., Frias R.L., Gainor J.F., Amzallag A., Greninger P., Lee D., Kalsy A., Gomez-Caraballo M., Elamine L., Howe E., Hur W., Lifshits E., Robinson H.E., Katayama R., Faber A.C., Awad M.M., Ramaswamy S., Mino-Kenudson M., Iafrate A.J., Benes C.H., Engelman J.A. Patient-derived models of acquired resistance can identify effective drug combinations for cancer. Science 2014, 346:1480-1486.
-
(2014)
Science
, vol.346
, pp. 1480-1486
-
-
Crystal, A.S.1
Shaw, A.T.2
Sequist, L.V.3
Friboulet, L.4
Niederst, M.J.5
Lockerman, E.L.6
Frias, R.L.7
Gainor, J.F.8
Amzallag, A.9
Greninger, P.10
Lee, D.11
Kalsy, A.12
Gomez-Caraballo, M.13
Elamine, L.14
Howe, E.15
Hur, W.16
Lifshits, E.17
Robinson, H.E.18
Katayama, R.19
Faber, A.C.20
Awad, M.M.21
Ramaswamy, S.22
Mino-Kenudson, M.23
Iafrate, A.J.24
Benes, C.H.25
Engelman, J.A.26
more..
-
15
-
-
10444280878
-
Strategies to overcome resistance to targeted protein kinase inhibitors
-
Daub H., Specht K., Ullrich A. Strategies to overcome resistance to targeted protein kinase inhibitors. Nat. Rev. Drug Discov. 2004, 3:1001-1010.
-
(2004)
Nat. Rev. Drug Discov.
, vol.3
, pp. 1001-1010
-
-
Daub, H.1
Specht, K.2
Ullrich, A.3
-
16
-
-
84876048479
-
Fibroblast growth factor receptor inhibitors as a cancer treatment: from a biologic rationale to medical perspectives
-
Dieci M.V., Arnedos M., Andre F., Soria J.C. Fibroblast growth factor receptor inhibitors as a cancer treatment: from a biologic rationale to medical perspectives. Cancer Discov. 2013, 3:264-279.
-
(2013)
Cancer Discov.
, vol.3
, pp. 264-279
-
-
Dieci, M.V.1
Arnedos, M.2
Andre, F.3
Soria, J.C.4
-
17
-
-
47249122523
-
Drug-sensitive FGFR2 mutations in endometrial carcinoma
-
Dutt A., Salvesen H.B., Chen T.H., Ramos A.H., Onofrio R.C., Hatton C., Nicoletti R., Winckler W., Grewal R., Hanna M., Wyhs N., Ziaugra L., Richter D.J., Trovik J., Engelsen I.B., Stefansson I.M., Fennell T., Cibulskis K., Zody M.C., Akslen L.A., Gabriel S., Wong K.K., Sellers W.R., Meyerson M., Greulich H. Drug-sensitive FGFR2 mutations in endometrial carcinoma. Proc. Natl. Acad. Sci. U. S. A. 2008, 105:8713-8717.
-
(2008)
Proc. Natl. Acad. Sci. U. S. A.
, vol.105
, pp. 8713-8717
-
-
Dutt, A.1
Salvesen, H.B.2
Chen, T.H.3
Ramos, A.H.4
Onofrio, R.C.5
Hatton, C.6
Nicoletti, R.7
Winckler, W.8
Grewal, R.9
Hanna, M.10
Wyhs, N.11
Ziaugra, L.12
Richter, D.J.13
Trovik, J.14
Engelsen, I.B.15
Stefansson, I.M.16
Fennell, T.17
Cibulskis, K.18
Zody, M.C.19
Akslen, L.A.20
Gabriel, S.21
Wong, K.K.22
Sellers, W.R.23
Meyerson, M.24
Greulich, H.25
more..
-
19
-
-
33344455174
-
Autophosphorylation of FGFR1 kinase is mediated by a sequential and precisely ordered reaction
-
Furdui C.M., Lew E.D., Schlessinger J., Anderson K.S. Autophosphorylation of FGFR1 kinase is mediated by a sequential and precisely ordered reaction. Mol. Cell 2006, 21:711-717.
-
(2006)
Mol. Cell
, vol.21
, pp. 711-717
-
-
Furdui, C.M.1
Lew, E.D.2
Schlessinger, J.3
Anderson, K.S.4
-
20
-
-
67649992842
-
Hybrid compound design to overcome the gatekeeper T338M mutation in cSrc
-
Getlik M., Grutter C., Simard J.R., Kluter S., Rabiller M., Rode H.B., Robubi A., Rauh D. Hybrid compound design to overcome the gatekeeper T338M mutation in cSrc. J. Med. Chem. 2009, 52:3915-3926.
-
(2009)
J. Med. Chem.
, vol.52
, pp. 3915-3926
-
-
Getlik, M.1
Grutter, C.2
Simard, J.R.3
Kluter, S.4
Rabiller, M.5
Rode, H.B.6
Robubi, A.7
Rauh, D.8
-
21
-
-
84855503769
-
The rise and fall of gatekeeper mutations? The BCR-ABL1 T315I paradigm
-
Gibbons D.L., Pricl S., Kantarjian H., Cortes J., Quintas-Cardama A. The rise and fall of gatekeeper mutations? The BCR-ABL1 T315I paradigm. Cancer 2012, 118:293-299.
-
(2012)
Cancer
, vol.118
, pp. 293-299
-
-
Gibbons, D.L.1
Pricl, S.2
Kantarjian, H.3
Cortes, J.4
Quintas-Cardama, A.5
-
22
-
-
0035800507
-
Clinical resistance to STI-571 cancer therapy caused by BCR-ABL gene mutation or amplification
-
Gorre M.E., Mohammed M., Ellwood K., Hsu N., Paquette R., Rao P.N., Sawyers C.L. Clinical resistance to STI-571 cancer therapy caused by BCR-ABL gene mutation or amplification. Science 2001, 293:876-880.
-
(2001)
Science
, vol.293
, pp. 876-880
-
-
Gorre, M.E.1
Mohammed, M.2
Ellwood, K.3
Hsu, N.4
Paquette, R.5
Rao, P.N.6
Sawyers, C.L.7
-
23
-
-
84859402751
-
Ponatinib (AP24534), a multitargeted pan-FGFR inhibitor with activity in multiple FGFR-amplified or mutated cancer models
-
Gozgit J.M., Wong M.J., Moran L., Wardwell S., Mohemmad Q.K., Narasimhan N.I., Shakespeare W.C., Wang F., Clackson T., Rivera V.M. Ponatinib (AP24534), a multitargeted pan-FGFR inhibitor with activity in multiple FGFR-amplified or mutated cancer models. Mol. Cancer Ther. 2012, 11:690-699.
-
(2012)
Mol. Cancer Ther.
, vol.11
, pp. 690-699
-
-
Gozgit, J.M.1
Wong, M.J.2
Moran, L.3
Wardwell, S.4
Mohemmad, Q.K.5
Narasimhan, N.I.6
Shakespeare, W.C.7
Wang, F.8
Clackson, T.9
Rivera, V.M.10
-
24
-
-
79955667838
-
Targeting mutant fibroblast growth factor receptors in cancer
-
Greulich H., Pollock P.M. 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
-
25
-
-
84921373464
-
DFG-out mode of inhibition by an irreversible type-1 inhibitor capable of overcoming gate-keeper mutations in FGF receptors
-
Huang Z., Tan L., Wang H., Liu Y., Blais S., Deng J., Neubert T.A., Gray N.S., Li X., Mohammadi M. DFG-out mode of inhibition by an irreversible type-1 inhibitor capable of overcoming gate-keeper mutations in FGF receptors. ACS Chem. Biol. 2015, 10:299-309.
-
(2015)
ACS Chem. Biol.
, vol.10
, pp. 299-309
-
-
Huang, Z.1
Tan, L.2
Wang, H.3
Liu, Y.4
Blais, S.5
Deng, J.6
Neubert, T.A.7
Gray, N.S.8
Li, X.9
Mohammadi, M.10
-
26
-
-
84905492809
-
Processing of X-ray snapshots from crystals in random orientations
-
Kabsch W. Processing of X-ray snapshots from crystals in random orientations. Acta Crystallogr. D Biol. Crystallogr. 2014, 70:2204-2216.
-
(2014)
Acta Crystallogr. D Biol. Crystallogr.
, vol.70
, pp. 2204-2216
-
-
Kabsch, W.1
-
27
-
-
84887022715
-
Phase II study of dovitinib in patients with metastatic and/or unresectable gastrointestinal stromal tumours after failure of imatinib and sunitinib
-
Kang Y.K., Yoo C., Ryoo B.Y., Lee J.J., Tan E., Park I., Park J.H., Choi Y.J., Jo J., Ryu J.S., Ryu M.H. Phase II study of dovitinib in patients with metastatic and/or unresectable gastrointestinal stromal tumours after failure of imatinib and sunitinib. Br. J. Cancer 2013, 109:2309-2315.
-
(2013)
Br. J. Cancer
, vol.109
, pp. 2309-2315
-
-
Kang, Y.K.1
Yoo, C.2
Ryoo, B.Y.3
Lee, J.J.4
Tan, E.5
Park, I.6
Park, J.H.7
Choi, Y.J.8
Jo, J.9
Ryu, J.S.10
Ryu, M.H.11
-
28
-
-
13844317894
-
EGFR mutation and resistance of non-small-cell lung cancer to gefitinib
-
Kobayashi S., Boggon T.J., Dayaram T., Janne P.A., Kocher O., Meyerson M., Johnson B.E., Eck M.J., Tenen D.G., Halmos B. EGFR mutation and resistance of non-small-cell lung cancer to gefitinib. N. Engl. J. Med. 2005, 352:786-792.
-
(2005)
N. Engl. J. Med.
, vol.352
, pp. 786-792
-
-
Kobayashi, S.1
Boggon, T.J.2
Dayaram, T.3
Janne, P.A.4
Kocher, O.5
Meyerson, M.6
Johnson, B.E.7
Eck, M.J.8
Tenen, D.G.9
Halmos, B.10
-
29
-
-
84877679916
-
Activity of the fibroblast growth factor receptor inhibitors dovitinib (TKI258) and NVP-BGJ398 in human endometrial cancer cells
-
Konecny G.E., Kolarova T., O'Brien N.A., Winterhoff B., Yang G., Qi J., Qi Z., Venkatesan N., Ayala R., Luo T., Finn R.S., Kristof J., Galderisi C., Porta D.G., Anderson L., Shi M.M., Yovine A., Slamon D.J. Activity of the fibroblast growth factor receptor inhibitors dovitinib (TKI258) and NVP-BGJ398 in human endometrial cancer cells. Mol. Cancer Ther. 2013, 12:632-642.
-
(2013)
Mol. Cancer Ther.
, vol.12
, pp. 632-642
-
-
Konecny, G.E.1
Kolarova, T.2
O'Brien, N.A.3
Winterhoff, B.4
Yang, G.5
Qi, J.6
Qi, Z.7
Venkatesan, N.8
Ayala, R.9
Luo, T.10
Finn, R.S.11
Kristof, J.12
Galderisi, C.13
Porta, D.G.14
Anderson, L.15
Shi, M.M.16
Yovine, A.17
Slamon, D.J.18
-
30
-
-
78650875209
-
Small molecule FGF receptor inhibitors block FGFR-dependent urothelial carcinoma growth in vitro and in vivo
-
Lamont F.R., Tomlinson D.C., Cooper P.A., Shnyder S.D., Chester J.D., Knowles M.A. 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
-
31
-
-
84903289523
-
TC-1 overexpression promotes cell proliferation in human non-small cell lung cancer that can be inhibited by PD173074
-
Lei J., Li W., Yang Y., Lu Q., Zhang N., Bai G., Zhong D., Su K., Liu B., Li X., Wang Y., Wang X. TC-1 overexpression promotes cell proliferation in human non-small cell lung cancer that can be inhibited by PD173074. PLoS One 2014, 9:e100075.
-
(2014)
PLoS One
, vol.9
, pp. e100075
-
-
Lei, J.1
Li, W.2
Yang, Y.3
Lu, Q.4
Zhang, N.5
Bai, G.6
Zhong, D.7
Su, K.8
Liu, B.9
Li, X.10
Wang, Y.11
Wang, X.12
-
32
-
-
84895932502
-
Reductions in myeloid-derived suppressor cells and lung metastases using AZD4547 treatment of a metastatic murine breast tumor model
-
Liu L., Ye T.H., Han Y.P., Song H., Zhang Y.K., Xia Y., Wang N.Y., Xiong Y., Song X.J., Zhu Y.X., Li de L., Zeng J., Ran K., Peng C.T., Wei Y.Q., Yu L.T. Reductions in myeloid-derived suppressor cells and lung metastases using AZD4547 treatment of a metastatic murine breast tumor model. Cell. Physiol. Biochem. 2014, 33:633-645.
-
(2014)
Cell. Physiol. Biochem.
, vol.33
, pp. 633-645
-
-
Liu, L.1
Ye, T.H.2
Han, Y.P.3
Song, H.4
Zhang, Y.K.5
Xia, Y.6
Wang, N.Y.7
Xiong, Y.8
Song, X.J.9
Zhu, Y.X.10
Li de, L.11
Zeng, J.12
Ran, K.13
Peng, C.T.14
Wei, Y.Q.15
Yu, L.T.16
-
33
-
-
84856694630
-
The different flexibility of c-Src and c-Abl kinases regulates the accessibility of a druggable inactive conformation
-
Lovera S., Sutto L., Boubeva R., Scapozza L., Dolker N., Gervasio F.L. The different flexibility of c-Src and c-Abl kinases regulates the accessibility of a druggable inactive conformation. J. Am. Chem. Soc. 2012, 134:2496-2499.
-
(2012)
J. Am. Chem. Soc.
, vol.134
, pp. 2496-2499
-
-
Lovera, S.1
Sutto, L.2
Boubeva, R.3
Scapozza, L.4
Dolker, N.5
Gervasio, F.L.6
-
34
-
-
84911887331
-
Dovitinib: rationale, preclinical and early clinical data in urothelial carcinoma of the bladder
-
Mazzola C.R., Siddiqui K.M., Billia M., Chin J. Dovitinib: rationale, preclinical and early clinical data in urothelial carcinoma of the bladder. Exp. Opin. Investig. Drugs 2014, 1-10.
-
(2014)
Exp. Opin. Investig. Drugs
, pp. 1-10
-
-
Mazzola, C.R.1
Siddiqui, K.M.2
Billia, M.3
Chin, J.4
-
35
-
-
84886629236
-
Deciphering the structural basis of eukaryotic protein kinase regulation
-
Meharena H.S., Chang P., Keshwani M.M., Oruganty K., Nene A.K., Kannan N., Taylor S.S., Kornev A.P. Deciphering the structural basis of eukaryotic protein kinase regulation. PLoS Biol. 2013, 11:e1001680.
-
(2013)
PLoS Biol.
, vol.11
, pp. e1001680
-
-
Meharena, H.S.1
Chang, P.2
Keshwani, M.M.3
Oruganty, K.4
Nene, A.K.5
Kannan, N.6
Taylor, S.S.7
Kornev, A.P.8
-
36
-
-
0030598848
-
Structure of the FGF receptor tyrosine kinase domain reveals a novel autoinhibitory mechanism
-
Mohammadi M., Schlessinger J., Hubbard S.R. Structure of the FGF receptor tyrosine kinase domain reveals a novel autoinhibitory mechanism. Cell 1996, 86:577-587.
-
(1996)
Cell
, vol.86
, pp. 577-587
-
-
Mohammadi, M.1
Schlessinger, J.2
Hubbard, S.R.3
-
37
-
-
0032531929
-
Crystal structure of an angiogenesis inhibitor bound to the FGF receptor tyrosine kinase domain
-
Mohammadi M., Froum S., Hamby J.M., Schroeder M.C., Panek R.L., Lu G.H., Eliseenkova A.V., Green D., Schlessinger J., Hubbard S.R. Crystal structure of an angiogenesis inhibitor bound to the FGF receptor tyrosine kinase domain. EMBO J. 1998, 17:5896-5904.
-
(1998)
EMBO J.
, vol.17
, pp. 5896-5904
-
-
Mohammadi, M.1
Froum, S.2
Hamby, J.M.3
Schroeder, M.C.4
Panek, R.L.5
Lu, G.H.6
Eliseenkova, A.V.7
Green, D.8
Schlessinger, J.9
Hubbard, S.R.10
-
38
-
-
0014454095
-
Kinetics of the reversible inhibition of enzyme-catalysed reactions by tight-binding inhibitors
-
Morrison J.F. Kinetics of the reversible inhibition of enzyme-catalysed reactions by tight-binding inhibitors. Biochim. Biophys. Acta 1969, 185:269-286.
-
(1969)
Biochim. Biophys. Acta
, vol.185
, pp. 269-286
-
-
Morrison, J.F.1
-
39
-
-
84896713052
-
Dovitinib versus sorafenib for third-line targeted treatment of patients with metastatic renal cell carcinoma: an open-label, randomised phase 3 trial
-
Motzer R.J., Porta C., Vogelzang N.J., Sternberg C.N., Szczylik C., Zolnierek J., Kollmannsberger C., Rha S.Y., Bjarnason G.A., Melichar B., De Giorgi U., Grunwald V., Davis I.D., Lee J.L., Esteban E., Urbanowitz G., Cai C., Squires M., Marker M., Shi M.M., Escudier B. Dovitinib versus sorafenib for third-line targeted treatment of patients with metastatic renal cell carcinoma: an open-label, randomised phase 3 trial. Lancet Oncol. 2014, 15:286-296.
-
(2014)
Lancet Oncol.
, vol.15
, pp. 286-296
-
-
Motzer, R.J.1
Porta, C.2
Vogelzang, N.J.3
Sternberg, C.N.4
Szczylik, C.5
Zolnierek, J.6
Kollmannsberger, C.7
Rha, S.Y.8
Bjarnason, G.A.9
Melichar, B.10
De Giorgi, U.11
Grunwald, V.12
Davis, I.D.13
Lee, J.L.14
Esteban, E.15
Urbanowitz, G.16
Cai, C.17
Squires, M.18
Marker, M.19
Shi, M.M.20
Escudier, B.21
more..
-
40
-
-
84862285959
-
Protein-ligand crystal structures can guide the design of selective inhibitors of the FGFR tyrosine kinase
-
Norman R.A., Schott A.K., Andrews D.M., Breed J., Foote K.M., Garner A.P., Ogg D., Orme J.P., Pink J.H., Roberts K., Rudge D.A., Thomas A.P., Leach A.G. 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
-
41
-
-
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 W.C., Zhu X., Eide C.A., Rivera V.M., Wang F., Adrian L.T., Zhou T., Huang W.S., Xu Q., Metcalf C.A., Tyner J.W., Loriaux M.M., Corbin A.S., Wardwell S., Ning Y., Keats J.A., Wang Y., Sundaramoorthi R., Thomas M., Zhou D., Snodgrass J., Commodore L., Sawyer T.K., Dalgarno D.C., Deininger M.W., Druker B.J., Clackson T. 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
Keats, J.A.17
Wang, Y.18
Sundaramoorthi, R.19
Thomas, M.20
Zhou, D.21
Snodgrass, J.22
Commodore, L.23
Sawyer, T.K.24
Dalgarno, D.C.25
Deininger, M.W.26
Druker, B.J.27
Clackson, T.28
more..
-
42
-
-
18244371651
-
Acquired resistance of lung adenocarcinomas to gefitinib or erlotinib is associated with a second mutation in the EGFR kinase domain
-
Pao W., Miller V.A., Politi K.A., Riely G.J., Somwar R., Zakowski M.F., Kris M.G., Varmus H. Acquired resistance of lung adenocarcinomas to gefitinib or erlotinib is associated with a second mutation in the EGFR kinase domain. PLoS Med. 2005, 2:e73.
-
(2005)
PLoS Med.
, vol.2
, pp. e73
-
-
Pao, W.1
Miller, V.A.2
Politi, K.A.3
Riely, G.J.4
Somwar, R.5
Zakowski, M.F.6
Kris, M.G.7
Varmus, H.8
-
43
-
-
84880875969
-
FGFR2 signaling underlies p63 oncogenic function in squamous cell carcinoma
-
Ramsey M.R., Wilson C., Ory B., Rothenberg S.M., Faquin W., Mills A.A., Ellisen L.W. FGFR2 signaling underlies p63 oncogenic function in squamous cell carcinoma. J. Clin. Invest. 2013, 123:3525-3538.
-
(2013)
J. Clin. Invest.
, vol.123
, pp. 3525-3538
-
-
Ramsey, M.R.1
Wilson, C.2
Ory, B.3
Rothenberg, S.M.4
Faquin, W.5
Mills, A.A.6
Ellisen, L.W.7
-
44
-
-
60549084927
-
Design, structure-activity relationships and in vivo characterization of 4-amino-3-benzimidazol-2-ylhydroquinolin-2-ones: a novel class of receptor tyrosine kinase inhibitors
-
Renhowe P.A., Pecchi S., Shafer C.M., Machajewski T.D., Jazan E.M., Taylor C., Antonios-McCrea W., McBride C.M., Frazier K., Wiesmann M., Lapointe G.R., Feucht P.H., Warne R.L., Heise C.C., Menezes D., Aardalen K., Ye H., He M., Le V., Vora J., Jansen J.M., Wernette-Hammond M.E., Harris A.L. Design, structure-activity relationships and in vivo characterization of 4-amino-3-benzimidazol-2-ylhydroquinolin-2-ones: a novel class of receptor tyrosine kinase inhibitors. J. Med. Chem. 2009, 52:278-292.
-
(2009)
J. Med. Chem.
, vol.52
, pp. 278-292
-
-
Renhowe, P.A.1
Pecchi, S.2
Shafer, C.M.3
Machajewski, T.D.4
Jazan, E.M.5
Taylor, C.6
Antonios-McCrea, W.7
McBride, C.M.8
Frazier, K.9
Wiesmann, M.10
Lapointe, G.R.11
Feucht, P.H.12
Warne, R.L.13
Heise, C.C.14
Menezes, D.15
Aardalen, K.16
Ye, H.17
He, M.18
Le, V.19
Vora, J.20
Jansen, J.M.21
Wernette-Hammond, M.E.22
Harris, A.L.23
more..
-
45
-
-
84878872190
-
FGFR fusions in the driver's seat
-
Sabnis A.J., Bivona T.G. FGFR fusions in the driver's seat. Cancer Discov. 2013, 3:607-609.
-
(2013)
Cancer Discov.
, vol.3
, pp. 607-609
-
-
Sabnis, A.J.1
Bivona, T.G.2
-
46
-
-
0001686739
-
Multiple BCR-ABL kinase domain mutations confer polyclonal resistance to the tyrosine kinase inhibitor imatinib (STI571) in chronic phase and blast crisis chronic myeloid leukemia
-
Shah N.P., Nicoll J.M., Nagar B., Gorre M.E., Paquette R.L., Kuriyan J., Sawyers C.L. Multiple BCR-ABL kinase domain mutations confer polyclonal resistance to the tyrosine kinase inhibitor imatinib (STI571) in chronic phase and blast crisis chronic myeloid leukemia. Cancer Cell 2002, 2:117-125.
-
(2002)
Cancer Cell
, vol.2
, pp. 117-125
-
-
Shah, N.P.1
Nicoll, J.M.2
Nagar, B.3
Gorre, M.E.4
Paquette, R.L.5
Kuriyan, J.6
Sawyers, C.L.7
-
47
-
-
84860870716
-
Oncogenic mutations counteract intrinsic disorder in the EGFR kinase and promote receptor dimerization
-
Shan Y., Eastwood M.P., Zhang X., Kim E.T., Arkhipov A., Dror R.O., Jumper J., Kuriyan J., Shaw D.E. Oncogenic mutations counteract intrinsic disorder in the EGFR kinase and promote receptor dimerization. Cell 2012, 149:860-870.
-
(2012)
Cell
, vol.149
, pp. 860-870
-
-
Shan, Y.1
Eastwood, M.P.2
Zhang, X.3
Kim, E.T.4
Arkhipov, A.5
Dror, R.O.6
Jumper, J.7
Kuriyan, J.8
Shaw, D.E.9
-
48
-
-
84856555606
-
Oncogene mutation profiling of pediatric solid tumors reveals significant subsets of embryonal rhabdomyosarcoma and neuroblastoma with mutated genes in growth signaling pathways
-
Shukla N., Ameur N., Yilmaz I., Nafa K., Lau C.Y., Marchetti A., Borsu L., Barr F.G., Ladanyi M. Oncogene mutation profiling of pediatric solid tumors reveals significant subsets of embryonal rhabdomyosarcoma and neuroblastoma with mutated genes in growth signaling pathways. Clin. Cancer Res. 2012, 18:748-757.
-
(2012)
Clin. Cancer Res.
, vol.18
, pp. 748-757
-
-
Shukla, N.1
Ameur, N.2
Yilmaz, I.3
Nafa, K.4
Lau, C.Y.5
Marchetti, A.6
Borsu, L.7
Barr, F.G.8
Ladanyi, M.9
-
49
-
-
84865805666
-
Transforming fusions of FGFR and TACC genes in human glioblastoma
-
Singh D., Chan J.M., Zoppoli P., Niola F., Sullivan R., Castano A., Liu E.M., Reichel J., Porrati P., Pellegatta S., Qiu K., Gao Z., Ceccarelli M., Riccardi R., Brat D.J., Guha A., Aldape K., Golfinos J.G., Zagzag D., Mikkelsen T., Finocchiaro G., Lasorella A., Rabadan R., Iavarone A. Transforming fusions of FGFR and TACC genes in human glioblastoma. Science 2012, 337:1231-1235.
-
(2012)
Science
, vol.337
, pp. 1231-1235
-
-
Singh, D.1
Chan, J.M.2
Zoppoli, P.3
Niola, F.4
Sullivan, R.5
Castano, A.6
Liu, E.M.7
Reichel, J.8
Porrati, P.9
Pellegatta, S.10
Qiu, K.11
Gao, Z.12
Ceccarelli, M.13
Riccardi, R.14
Brat, D.J.15
Guha, A.16
Aldape, K.17
Golfinos, J.G.18
Zagzag, D.19
Mikkelsen, T.20
Finocchiaro, G.21
Lasorella, A.22
Rabadan, R.23
Iavarone, A.24
more..
-
50
-
-
84879510153
-
Effects of oncogenic mutations on the conformational free-energy landscape of EGFR kinase
-
Sutto L., Gervasio F.L. Effects of oncogenic mutations on the conformational free-energy landscape of EGFR kinase. Proc. Natl. Acad. Sci. U. S. A. 2013, 110:10616-10621.
-
(2013)
Proc. Natl. Acad. Sci. U. S. A.
, vol.110
, pp. 10616-10621
-
-
Sutto, L.1
Gervasio, F.L.2
-
51
-
-
33749824425
-
Functional analyses and molecular modeling of two c-Kit mutations responsible for imatinib secondary resistance in GIST patients
-
Tamborini E., Pricl S., Negri T., Lagonigro M.S., Miselli F., Greco A., Gronchi A., Casali P.G., Ferrone M., Fermeglia M., Carbone A., Pierotti M.A., Pilotti S. Functional analyses and molecular modeling of two c-Kit mutations responsible for imatinib secondary resistance in GIST patients. Oncogene 2006, 25:6140-6146.
-
(2006)
Oncogene
, vol.25
, pp. 6140-6146
-
-
Tamborini, E.1
Pricl, S.2
Negri, T.3
Lagonigro, M.S.4
Miselli, F.5
Greco, A.6
Gronchi, A.7
Casali, P.G.8
Ferrone, M.9
Fermeglia, M.10
Carbone, A.11
Pierotti, M.A.12
Pilotti, S.13
-
52
-
-
84909594628
-
Development of covalent inhibitors that can overcome resistance to first-generation FGFR kinase inhibitors
-
Tan L., Wang J., Tanizaki J., Huang Z., Aref A.R., Rusan M., Zhu S.J., Zhang Y., Ercan D., Liao R.G., Capelletti M., Zhou W., Hur W., Kim N., Sim T., Gaudet S., Barbie D.A., Yeh J.R., Yun C.H., Hammerman P.S., Mohammadi M., Janne P.A., Gray N.S. Development of covalent inhibitors that can overcome resistance to first-generation FGFR kinase inhibitors. Proc. Natl. Acad. Sci. U. S. A. 2014, 111:E4869-E4877.
-
(2014)
Proc. Natl. Acad. Sci. U. S. A.
, vol.111
, pp. E4869-E4877
-
-
Tan, L.1
Wang, J.2
Tanizaki, J.3
Huang, Z.4
Aref, A.R.5
Rusan, M.6
Zhu, S.J.7
Zhang, Y.8
Ercan, D.9
Liao, R.G.10
Capelletti, M.11
Zhou, W.12
Hur, W.13
Kim, N.14
Sim, T.15
Gaudet, S.16
Barbie, D.A.17
Yeh, J.R.18
Yun, C.H.19
Hammerman, P.S.20
Mohammadi, M.21
Janne, P.A.22
Gray, N.S.23
more..
-
53
-
-
70449450426
-
Identification of FGFR4-activating mutations in human rhabdomyosarcomas that promote metastasis in xenotransplanted models
-
Taylor J.G.T., Cheuk A.T., Tsang P.S., Chung J.Y., Song Y.K., Desai K., Yu Y., Chen Q.R., Shah K., Youngblood V., Fang J., Kim S.Y., Yeung C., Helman L.J., Mendoza A., Ngo V., Staudt L.M., Wei J.S., Khanna C., Catchpoole D., Qualman S.J., Hewitt S.M., Merlino G., Chanock S.J., Khan J. 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.G.T.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
Staudt, L.M.17
Wei, J.S.18
Khanna, C.19
Catchpoole, D.20
Qualman, S.J.21
Hewitt, S.M.22
Merlino, G.23
Chanock, S.J.24
Khan, J.25
more..
-
54
-
-
75149170979
-
Fibroblast growth factor signalling: from development to cancer
-
Turner N., 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
-
55
-
-
77950278598
-
FGFR1 amplification drives endocrine therapy resistance and is a therapeutic target in breast cancer
-
Turner N., Pearson A., Sharpe R., Lambros M., Geyer F., Lopez-Garcia M.A., Natrajan R., Marchio C., Iorns E., Mackay A., et al. FGFR1 amplification drives endocrine therapy resistance and is a therapeutic target in breast cancer. Cancer Res. 2010, 70:2085-2094.
-
(2010)
Cancer Res.
, vol.70
, pp. 2085-2094
-
-
Turner, N.1
Pearson, A.2
Sharpe, R.3
Lambros, M.4
Geyer, F.5
Lopez-Garcia, M.A.6
Natrajan, R.7
Marchio, C.8
Iorns, E.9
Mackay, A.10
-
56
-
-
79960092299
-
Rapid and accurate ranking of binding affinities of epidermal growth factor receptor sequences with selected lung cancer drugs
-
Wan S., Coveney P.V. Rapid and accurate ranking of binding affinities of epidermal growth factor receptor sequences with selected lung cancer drugs. J. R. Soc. Interface 2011, 8:1114-1127.
-
(2011)
J. R. Soc. Interface
, vol.8
, pp. 1114-1127
-
-
Wan, S.1
Coveney, P.V.2
-
57
-
-
79959713140
-
Fibroblast growth factors and their receptors in cancer
-
Wesche J., Haglund K., Haugsten E.M. 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
-
59
-
-
84864286442
-
Widespread potential for growth-factor-driven resistance to anticancer kinase inhibitors
-
Wilson T.R., Fridlyand J., Yan Y., Penuel E., Burton L., Chan E., Peng J., Lin E., Wang Y., Sosman J., Ribas A., Li J., Moffat J., Sutherlin D.P., Koeppen H., Merchant M., Neve R., Settleman J. Widespread potential for growth-factor-driven resistance to anticancer kinase inhibitors. Nature 2012, 487:505-509.
-
(2012)
Nature
, vol.487
, pp. 505-509
-
-
Wilson, T.R.1
Fridlyand, J.2
Yan, Y.3
Penuel, E.4
Burton, L.5
Chan, E.6
Peng, J.7
Lin, E.8
Wang, Y.9
Sosman, J.10
Ribas, A.11
Li, J.12
Moffat, J.13
Sutherlin, D.P.14
Koeppen, H.15
Merchant, M.16
Neve, R.17
Settleman, J.18
-
60
-
-
79953737180
-
Overview of the CCP4 suite and current developments
-
Winn M.D., Ballard C.C., Cowtan K.D., Dodson E.J., Emsley P., Evans P.R., Keegan R.M., Krissinel E.B., Leslie A.G., McCoy A., Mcnicholas S.J., Murshudov G.N., Pannu N.S., Potterton E.A., Powell H.R., Read R.J., Vagin A., Wilson K.S. Overview of the CCP4 suite and current developments. Acta Crystallogr. D Biol. Crystallogr. 2011, 67:235-242.
-
(2011)
Acta Crystallogr. D Biol. Crystallogr.
, vol.67
, pp. 235-242
-
-
Winn, M.D.1
Ballard, C.C.2
Cowtan, K.D.3
Dodson, E.J.4
Emsley, P.5
Evans, P.R.6
Keegan, R.M.7
Krissinel, E.B.8
Leslie, A.G.9
McCoy, A.10
Mcnicholas, S.J.11
Murshudov, G.N.12
Pannu, N.S.13
Potterton, E.A.14
Powell, H.R.15
Read, R.J.16
Vagin, A.17
Wilson, K.S.18
-
62
-
-
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 P.R., Zhang J., Kilgour E., Zhang X., Ji Q. 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
Kilgour, E.17
Zhang, X.18
Ji, Q.19
-
63
-
-
84894027173
-
Inhibition of FGFR signaling by PD173074 improves antitumor immunity and impairs breast cancer metastasis
-
Ye T., Wei X., Yin T., Xia Y., Li D., Shao B., Song X., He S., Luo M., Gao X., He Z., Luo C., Xiong Y., Wang N., Zeng J., Zhao L., Shen G., Xie Y., Yu L., Wei Y. Inhibition of FGFR signaling by PD173074 improves antitumor immunity and impairs breast cancer metastasis. Breast Cancer Res. Treat. 2014, 143:435-446.
-
(2014)
Breast Cancer Res. Treat.
, vol.143
, pp. 435-446
-
-
Ye, T.1
Wei, X.2
Yin, T.3
Xia, Y.4
Li, D.5
Shao, B.6
Song, X.7
He, S.8
Luo, M.9
Gao, X.10
He, Z.11
Luo, C.12
Xiong, Y.13
Wang, N.14
Zeng, J.15
Zhao, L.16
Shen, G.17
Xie, Y.18
Yu, L.19
Wei, Y.20
more..
-
64
-
-
40049099220
-
The T790M mutation in EGFR kinase causes drug resistance by increasing the affinity for ATP
-
Yun C.H., Mengwasser K.E., Toms A.V., Woo M.S., Greulich H., Wong K.K., Meyerson M., Eck M.J. 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
-
65
-
-
72949092456
-
Novel mutant-selective EGFR kinase inhibitors against EGFR T790M
-
Zhou W., Ercan D., Chen L., Yun C.H., Li D., Capelletti M., Cortot A.B., Chirieac L., Iacob R.E., Padera R., Engen J.R., Wong K.K., Eck M.J., Gray N.S., Janne P.A. Novel mutant-selective EGFR kinase inhibitors against EGFR T790M. Nature 2009, 462:1070-1074.
-
(2009)
Nature
, vol.462
, pp. 1070-1074
-
-
Zhou, W.1
Ercan, D.2
Chen, L.3
Yun, C.H.4
Li, D.5
Capelletti, M.6
Cortot, A.B.7
Chirieac, L.8
Iacob, R.E.9
Padera, R.10
Engen, J.R.11
Wong, K.K.12
Eck, M.J.13
Gray, N.S.14
Janne, P.A.15
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