-
2
-
-
84897901864
-
Bruton's tyrosine kinase (BTK) function is important to the development and expansion of chronic lymphocytic leukemia (CLL)
-
Woyach JA, Bojnik E, Ruppert AS, Stefanovski MR, Goettl VM, Smucker KA, Smith LL, Dubovsky JA, Towns WH, MacMurray J, Harrington BK, Davis ME, Gobessi S, Laurenti L, Chang BY, Buggy JJ, et al. Bruton's tyrosine kinase (BTK) function is important to the development and expansion of chronic lymphocytic leukemia (CLL). Blood. 2014; 123:1207-1213.
-
(2014)
Blood
, vol.123
, pp. 1207-1213
-
-
Woyach, J.A.1
Bojnik, E.2
Ruppert, A.S.3
Stefanovski, M.R.4
Goettl, V.M.5
Smucker, K.A.6
Smith, L.L.7
Dubovsky, J.A.8
Towns, W.H.9
MacMurray, J.10
Harrington, B.K.11
Davis, M.E.12
Gobessi, S.13
Laurenti, L.14
Chang, B.Y.15
Buggy, J.J.16
-
3
-
-
84922787400
-
Combination of ibrutinib with ABT-199: synergistic effects on proliferation inhibition and apoptosis in mantle cell lymphoma cells through perturbation of BTK, AKT and BCL2 pathways
-
Zhao X, Bodo J, Sun D, Durkin L, Lin J, Smith MR, Hsi ED. Combination of ibrutinib with ABT-199: synergistic effects on proliferation inhibition and apoptosis in mantle cell lymphoma cells through perturbation of BTK, AKT and BCL2 pathways. British journal of haematology. 2015; 168:765-8.
-
(2015)
British journal of haematology
, vol.168
, pp. 765-768
-
-
Zhao, X.1
Bodo, J.2
Sun, D.3
Durkin, L.4
Lin, J.5
Smith, M.R.6
Hsi, E.D.7
-
4
-
-
84897853580
-
Identification of Bruton's tyrosine kinase as a therapeutic target in acute myeloid leukemia
-
Rushworth SA, Murray MY, Zaitseva L, Bowles KM, MacEwan DJ. Identification of Bruton's tyrosine kinase as a therapeutic target in acute myeloid leukemia. Blood. 2014; 123:1229-1238.
-
(2014)
Blood
, vol.123
, pp. 1229-1238
-
-
Rushworth, S.A.1
Murray, M.Y.2
Zaitseva, L.3
Bowles, K.M.4
MacEwan, D.J.5
-
5
-
-
84881225049
-
Targeting BTK with ibrutinib in relapsed or refractory mantle-cell lymphoma
-
Wang ML, Rule S, Martin P, Goy A, Auer R, Kahl BS, Jurczak W, Advani RH, Romaguera JE, Williams ME, Barrientos JC, Chmielowska E, Radford J, Stilgenbauer S, Dreyling M, Jedrzejczak WW, et al. Targeting BTK with ibrutinib in relapsed or refractory mantle-cell lymphoma. The New England journal of medicine. 2013; 369:507-516.
-
(2013)
The New England journal of medicine
, vol.369
, pp. 507-516
-
-
Wang, M.L.1
Rule, S.2
Martin, P.3
Goy, A.4
Auer, R.5
Kahl, B.S.6
Jurczak, W.7
Advani, R.H.8
Romaguera, J.E.9
Williams, M.E.10
Barrientos, J.C.11
Chmielowska, E.12
Radford, J.13
Stilgenbauer, S.14
Dreyling, M.15
Jedrzejczak, W.W.16
-
6
-
-
84879748062
-
Targeting BTK with ibrutinib in relapsed chronic lymphocytic leukemia
-
Byrd JC, Furman RR, Coutre SE, Flinn IW, Burger JA, Blum KA, Grant B, Sharman JP, Coleman M, Wierda WG, Jones JA, Zhao W, Heerema NA, Johnson AJ, Sukbuntherng J, Chang BY, et al. Targeting BTK with ibrutinib in relapsed chronic lymphocytic leukemia. The New England journal of medicine. 2013; 369:32-42.
-
(2013)
The New England journal of medicine
, vol.369
, pp. 32-42
-
-
Byrd, J.C.1
Furman, R.R.2
Coutre, S.E.3
Flinn, I.W.4
Burger, J.A.5
Blum, K.A.6
Grant, B.7
Sharman, J.P.8
Coleman, M.9
Wierda, W.G.10
Jones, J.A.11
Zhao, W.12
Heerema, N.A.13
Johnson, A.J.14
Sukbuntherng, J.15
Chang, B.Y.16
-
7
-
-
84867589196
-
BTK inhibitor ibrutinib is cytotoxic to myeloma and potently enhances bortezomib and lenalidomide activities through NF-kappaB
-
Rushworth SA, Bowles KM, Barrera LN, Murray MY, Zaitseva L, MacEwan DJ. BTK inhibitor ibrutinib is cytotoxic to myeloma and potently enhances bortezomib and lenalidomide activities through NF-kappaB. Cellular signalling. 2013; 25:106-112.
-
(2013)
Cellular signalling
, vol.25
, pp. 106-112
-
-
Rushworth, S.A.1
Bowles, K.M.2
Barrera, L.N.3
Murray, M.Y.4
Zaitseva, L.5
MacEwan, D.J.6
-
8
-
-
84874405894
-
Bruton's Tyrosine Kinase mediates platelet receptor-induced generation of microparticles: a potential mechanism for amplification of inflammatory responses in rheumatoid arthritis synovial joints
-
Hsu J, Gu Y, Tan SL, Narula S, DeMartino JA, Liao C. Bruton's Tyrosine Kinase mediates platelet receptor-induced generation of microparticles: a potential mechanism for amplification of inflammatory responses in rheumatoid arthritis synovial joints. Immunology letters. 2013; 150:97-104.
-
(2013)
Immunology letters
, vol.150
, pp. 97-104
-
-
Hsu, J.1
Gu, Y.2
Tan, S.L.3
Narula, S.4
DeMartino, J.A.5
Liao, C.6
-
9
-
-
79960133279
-
The Bruton tyrosine kinase inhibitor PCI-32765 ameliorates autoimmune arthritis by inhibition of multiple effector cells
-
Chang BY, Huang MM, Francesco M, Chen J, Sokolove J, Magadala P, Robinson WH, Buggy JJ. The Bruton tyrosine kinase inhibitor PCI-32765 ameliorates autoimmune arthritis by inhibition of multiple effector cells. Arthritis research & therapy. 2011; 13:R115.
-
(2011)
Arthritis research & therapy
, vol.13
, pp. R115
-
-
Chang, B.Y.1
Huang, M.M.2
Francesco, M.3
Chen, J.4
Sokolove, J.5
Magadala, P.6
Robinson, W.H.7
Buggy, J.J.8
-
10
-
-
77955625479
-
The Bruton tyrosine kinase inhibitor PCI-32765 blocks B-cell activation and is efficacious in models of autoimmune disease and B-cell malignancy
-
Honigberg LA, Smith AM, Sirisawad M, Verner E, Loury D, Chang B, Li S, Pan Z, Thamm DH, Miller RA, Buggy JJ. The Bruton tyrosine kinase inhibitor PCI-32765 blocks B-cell activation and is efficacious in models of autoimmune disease and B-cell malignancy. Proceedings of the National Academy of Sciences of the United States of America. 2010; 107:13075-13080.
-
(2010)
Proceedings of the National Academy of Sciences of the United States of America
, vol.107
, pp. 13075-13080
-
-
Honigberg, L.A.1
Smith, A.M.2
Sirisawad, M.3
Verner, E.4
Loury, D.5
Chang, B.6
Li, S.7
Pan, Z.8
Thamm, D.H.9
Miller, R.A.10
Buggy, J.J.11
-
11
-
-
0034992521
-
The epidermal growth factor receptor family as a central element for cellular signal transduction and diversification
-
Prenzel N, Fischer OM, Streit S, Hart S, Ullrich A. The epidermal growth factor receptor family as a central element for cellular signal transduction and diversification. Endocrine-related cancer. 2001; 8:11-31.
-
(2001)
Endocrine-related cancer
, vol.8
, pp. 11-31
-
-
Prenzel, N.1
Fischer, O.M.2
Streit, S.3
Hart, S.4
Ullrich, A.5
-
14
-
-
13844317894
-
EGFR mutation and resistance of non-small-cell lung cancer to gefitinib
-
Kobayashi S, Boggon TJ, Dayaram T, Janne PA, Kocher O, Meyerson M, Johnson BE, Eck MJ, Tenen DG, Halmos B. EGFR mutation and resistance of non-small-cell lung cancer to gefitinib. The New England journal of medicine. 2005; 352:786-792.
-
(2005)
The New England journal of medicine
, 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
-
15
-
-
18244371651
-
Acquired resistance of lung adenocarcinomas to gefitinib or erlotinib is associated with a second mutation in the EGFR kinase domain
-
Pao W, Miller VA, Politi KA, Riely GJ, Somwar R, Zakowski MF, Kris MG, Varmus H. Acquired resistance of lung adenocarcinomas to gefitinib or erlotinib is associated with a second mutation in the EGFR kinase domain. PLoS medicine. 2005; 2:e73.
-
(2005)
PLoS medicine
, vol.2
-
-
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
-
16
-
-
49149118719
-
BIBW2992, an irreversible EGFR/HER2 inhibitor highly effective in preclinical lung cancer models
-
Li D, Ambrogio L, Shimamura T, Kubo S, Takahashi M, Chirieac LR, Padera RF, Shapiro GI, Baum A, Himmelsbach F, Rettig WJ, Meyerson M, Solca F, Greulich H, Wong KK. BIBW2992, an irreversible EGFR/HER2 inhibitor highly effective in preclinical lung cancer models. Oncogene. 2008; 27:4702-4711.
-
(2008)
Oncogene
, vol.27
, pp. 4702-4711
-
-
Li, D.1
Ambrogio, L.2
Shimamura, T.3
Kubo, S.4
Takahashi, M.5
Chirieac, L.R.6
Padera, R.F.7
Shapiro, G.I.8
Baum, A.9
Himmelsbach, F.10
Rettig, W.J.11
Meyerson, M.12
Solca, F.13
Greulich, H.14
Wong, K.K.15
-
17
-
-
0034611617
-
Tyrosine kinase inhibitos. 17. Irreversible inhibitors of the epidermal growth factor receptor: 4-(phenylamino)quinazoline-and 4-(phenylamino) pyrido [3,2-d]pyrimidine-6-acrylamides bearing additional solubilizing functions
-
Smaill JB, Rewcastle GW, Loo JA, Greis KD, Chan OH, Reyner EL, Lipka E, Showalter HD, Vincent PW, Elliott WL, Denny WA. Tyrosine kinase inhibitors. 17. Irreversible inhibitors of the epidermal growth factor receptor: 4-(phenylamino)quinazoline-and 4-(phenylamino) pyrido [3,2-d]pyrimidine-6-acrylamides bearing additional solubilizing functions. Journal of medicinal chemistry. 2000; 43:1380-1397.
-
(2000)
Journal of medicinal chemistry
, vol.43
, pp. 1380-1397
-
-
Smaill, J.B.1
Rewcastle, G.W.2
Loo, J.A.3
Greis, K.D.4
Chan, O.H.5
Reyner, E.L.6
Lipka, E.7
Showalter, H.D.8
Vincent, P.W.9
Elliott, W.L.10
Denny, W.A.11
-
18
-
-
84858669035
-
Second-generation irreversible epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs): a better mousetrap? A review of the clinical evidence
-
Ou SH. Second-generation irreversible epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs): a better mousetrap? A review of the clinical evidence. Critical reviews in oncology/hematology. 2012; 83:407-421.
-
(2012)
Critical reviews in oncology/hematology
, vol.83
, pp. 407-421
-
-
Ou, S.H.1
-
19
-
-
84887977876
-
Discovery of a mutant-selective covalent inhibitor of EGFR that overcomes T790M-mediated resistance in NSCLC
-
Walter AO, Sjin RT, Haringsma HJ, Ohashi K, Sun J, Lee K, Dubrovskiy A, Labenski M, Zhu Z, Wang Z, Sheets M, St Martin T, Karp R, van Kalken D, Chaturvedi P, Niu D, et al. Discovery of a mutant-selective covalent inhibitor of EGFR that overcomes T790M-mediated resistance in NSCLC. Cancer discovery. 2013; 3:1404-1415.
-
(2013)
Cancer discovery
, vol.3
, pp. 1404-1415
-
-
Walter, A.O.1
Sjin, R.T.2
Haringsma, H.J.3
Ohashi, K.4
Sun, J.5
Lee, K.6
Dubrovskiy, A.7
Labenski, M.8
Zhu, Z.9
Wang, Z.10
Sheets, M.11
St Martin, T.12
Karp, R.13
van Kalken, D.14
Chaturvedi, P.15
Niu, D.16
-
20
-
-
84904898065
-
AZD9291, an irreversible EGFR TKI, overcomes T790M-mediated resistance to EGFR inhibitors in lung cancer
-
Cross DA, Ashton SE, Ghiorghiu S, Eberlein C, Nebhan CA, Spitzler PJ, Orme JP, Finlay MR, Ward RA, Mellor MJ, Hughes G, Rahi A, Jacobs VN, Red Brewer M, Ichihara E, Sun J, et al. AZD9291, an irreversible EGFR TKI, overcomes T790M-mediated resistance to EGFR inhibitors in lung cancer. Cancer discovery. 2014; 4:1046-1061.
-
(2014)
Cancer discovery
, vol.4
, pp. 1046-1061
-
-
Cross, D.A.1
Ashton, S.E.2
Ghiorghiu, S.3
Eberlein, C.4
Nebhan, C.A.5
Spitzler, P.J.6
Orme, J.P.7
Finlay, M.R.8
Ward, R.A.9
Mellor, M.J.10
Hughes, G.11
Rahi, A.12
Jacobs, V.N.13
Red Brewer, M.14
Ichihara, E.15
Sun, J.16
-
21
-
-
84922753595
-
Toward precision medicine with next-generation EGFR inhibitors in non-small-cell lung cancer
-
Yap TA, Popat S. Toward precision medicine with next-generation EGFR inhibitors in non-small-cell lung cancer. Pharmacogenomics and personalized medicine. 2014; 7:285-295.
-
(2014)
Pharmacogenomics and personalized medicine
, vol.7
, pp. 285-295
-
-
Yap, T.A.1
Popat, S.2
-
22
-
-
72949092456
-
Novel mutant-selective EGFR kinase inhibitors against EGFR T790M
-
Zhou W, Ercan D, Chen L, Yun CH, Li D, Capelletti M, Cortot AB, Chirieac L, Iacob RE, Padera R, Engen JR, Wong KK, Eck MJ, Gray NS, Janne PA. 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
-
23
-
-
84929465568
-
Selective antitumor activity of ibrutinib in EGFR-mutant non-small cell lung cancer cells
-
Gao W, Wang M, Wang L, Lu H, Wu S, Dai B, Ou Z, Zhang L, Heymach JV, Gold KA, Minna J, Roth JA, Hofstetter WL, Swisher SG, Fang B. Selective antitumor activity of ibrutinib in EGFR-mutant non-small cell lung cancer cells. Journal of the National Cancer Institute. 2014; 106. doi: 10.1093/jnci/dju204.
-
(2014)
Journal of the National Cancer Institute
, vol.106
-
-
Gao, W.1
Wang, M.2
Wang, L.3
Lu, H.4
Wu, S.5
Dai, B.6
Ou, Z.7
Zhang, L.8
Heymach, J.V.9
Gold, K.A.10
Minna, J.11
Roth, J.A.12
Hofstetter, W.L.13
Swisher, S.G.14
Fang, B.15
-
24
-
-
33751328082
-
ErbB receptors: new insights on mechanisms and biology
-
Linggi B, Carpenter G. ErbB receptors: new insights on mechanisms and biology. Trends in cell biology. 2006; 16:649-656.
-
(2006)
Trends in cell biology
, vol.16
, pp. 649-656
-
-
Linggi, B.1
Carpenter, G.2
-
25
-
-
70349684791
-
Dual targeting of EGFR can overcome a major drug resistance mutation in mouse models of EGFR mutant lung cancer
-
Regales L, Gong Y, Shen R, de Stanchina E, Vivanco I, Goel A, Koutcher JA, Spassova M, Ouerfelli O, Mellinghoff IK, Zakowski MF, Politi KA, Pao W. Dual targeting of EGFR can overcome a major drug resistance mutation in mouse models of EGFR mutant lung cancer. The Journal of clinical investigation. 2009; 119:3000-3010.
-
(2009)
The Journal of clinical investigation
, vol.119
, pp. 3000-3010
-
-
Regales, L.1
Gong, Y.2
Shen, R.3
de Stanchina, E.4
Vivanco, I.5
Goel, A.6
Koutcher, J.A.7
Spassova, M.8
Ouerfelli, O.9
Mellinghoff, I.K.10
Zakowski, M.F.11
Politi, K.A.12
Pao, W.13
-
26
-
-
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, Eck MJ. The T790M mutation in EGFR kinase causes drug resistance by increasing the affinity for ATP. Proceedings of the National Academy of Sciences of the United States of America. 2008; 105:2070-2075.
-
(2008)
Proceedings of the National Academy of Sciences of the United States of America
, 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
-
27
-
-
79958080372
-
Phase II trial of dasatinib for patients with acquired resistance to treatment with the epidermal growth factor receptor tyrosine kinase inhibitors erlotinib or gefitinib
-
Johnson ML, Riely GJ, Rizvi NA, Azzoli CG, Kris MG, Sima CS, Ginsberg MS, Pao W, Miller VA. Phase II trial of dasatinib for patients with acquired resistance to treatment with the epidermal growth factor receptor tyrosine kinase inhibitors erlotinib or gefitinib. Journal of thoracic oncology: official publication of the International Association for the Study of Lung Cancer. 2011; 6:1128-1131.
-
(2011)
Journal of thoracic oncology: official publication of the International Association for the Study of Lung Cancer
, vol.6
, pp. 1128-1131
-
-
Johnson, M.L.1
Riely, G.J.2
Rizvi, N.A.3
Azzoli, C.G.4
Kris, M.G.5
Sima, C.S.6
Ginsberg, M.S.7
Pao, W.8
Miller, V.A.9
-
28
-
-
84925269097
-
Overcoming EGFR T790M-based Tyrosine Kinase Inhibitor Resistance with an Allele-specific DNAzyme
-
Lai WY, Chen CY, Yang SC, Wu JY, Chang CJ, Yang PC, Peck K. Overcoming EGFR T790M-based Tyrosine Kinase Inhibitor Resistance with an Allele-specific DNAzyme. Molecular therapy Nucleic acids. 2014; 3:e150.
-
(2014)
Molecular therapy Nucleic acids
, vol.3
-
-
Lai, W.Y.1
Chen, C.Y.2
Yang, S.C.3
Wu, J.Y.4
Chang, C.J.5
Yang, P.C.6
Peck, K.7
-
29
-
-
38049084406
-
Discovery of selective irreversible inhibitors for Bruton's tyrosine kinase
-
Pan Z, Scheerens H, Li SJ, Schultz BE, Sprengeler PA, Burrill LC, Mendonca RV, Sweeney MD, Scott KC, Grothaus PG, Jeffery DA, Spoerke JM, Honigberg LA, Young PR, Dalrymple SA, Palmer JT. Discovery of selective irreversible inhibitors for Bruton's tyrosine kinase. ChemMedChem. 2007; 2:58-61.
-
(2007)
ChemMedChem
, vol.2
, pp. 58-61
-
-
Pan, Z.1
Scheerens, H.2
Li, S.J.3
Schultz, B.E.4
Sprengeler, P.A.5
Burrill, L.C.6
Mendonca, R.V.7
Sweeney, M.D.8
Scott, K.C.9
Grothaus, P.G.10
Jeffery, D.A.11
Spoerke, J.M.12
Honigberg, L.A.13
Young, P.R.14
Dalrymple, S.A.15
Palmer, J.T.16
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