-
1
-
-
0027441332
-
The gene involved in X-linked agammaglobulinaemia is a member of the src family of protein-tyrosine kinases
-
Vetrie D, Vorechovsky I, Sideras P, Holland J, Davies A, Flinter F et al. The gene involved in X-linked agammaglobulinaemia is a member of the src family of protein-tyrosine kinases. Nature 1993; 361: 226-233.
-
(1993)
Nature
, vol.361
, pp. 226-233
-
-
Vetrie, D.1
Vorechovsky, I.2
Sideras, P.3
Holland, J.4
Davies, A.5
Flinter, F.6
-
2
-
-
0027399081
-
Deficient expression of a B cell cytoplasmic tyrosine kinase in human X-linked agammaglobulinemia
-
Tsukada S, Saffran DC, Rawlings DJ, Parolini O, Allen RC, Klisak I et al. Deficient expression of a B cell cytoplasmic tyrosine kinase in human X-linked agammaglobulinemia. Cell 1993; 72: 279-290.
-
(1993)
Cell
, vol.72
, pp. 279-290
-
-
Tsukada, S.1
Saffran, D.C.2
Rawlings, D.J.3
Parolini, O.4
Allen, R.C.5
Klisak, I.6
-
3
-
-
84871765731
-
Targeting B-Cell receptor signaling for anticancer therapy: The Bruton's tyrosine kinase inhibitor ibrutinib induces impressive responses in B-cell malignancies
-
Wiestner A. Targeting B-Cell receptor signaling for anticancer therapy: the Bruton's tyrosine kinase inhibitor ibrutinib induces impressive responses in B-cell malignancies. J Clin Oncol 2013; 31: 128-130.
-
(2013)
J Clin Oncol
, vol.31
, pp. 128-130
-
-
Wiestner, A.1
-
4
-
-
84897055483
-
Targeting Bruton's tyrosine kinase in B cell malignancies
-
Hendriks RW, Yuvaraj S, Kil LP. Targeting Bruton's tyrosine kinase in B cell malignancies. Nat Rev Cancer 2014; 14: 219-232.
-
(2014)
Nat Rev Cancer
, vol.14
, pp. 219-232
-
-
Hendriks, R.W.1
Yuvaraj, S.2
Kil, L.P.3
-
5
-
-
0028151518
-
Bruton tyrosine kinase is tyrosine phosphorylated and activated in pre-B lymphocytes and receptor-ligated B cells
-
Aoki Y, Isselbacher KJ, Pillai S. Bruton tyrosine kinase is tyrosine phosphorylated and activated in pre-B lymphocytes and receptor-ligated B cells. Proc Natl Acad Sci USA 1994; 91: 10606-10609.
-
(1994)
Proc Natl Acad Sci USA
, vol.91
, pp. 10606-10609
-
-
Aoki, Y.1
Isselbacher, K.J.2
Pillai, S.3
-
6
-
-
0033959733
-
BLNK: Connecting Syk and Btk to calcium signals
-
Kurosaki T, Tsukada S. BLNK: connecting Syk and Btk to calcium signals. Immunity 2000; 12: 1-5.
-
(2000)
Immunity
, vol.12
, pp. 1-5
-
-
Kurosaki, T.1
Tsukada, S.2
-
8
-
-
84875032090
-
Novel Bruton's tyrosine kinase inhibitors currently in development
-
D'Cruz OJ, Uckun FM. Novel Bruton's tyrosine kinase inhibitors currently in development. Onco Targets Ther 2013; 6: 161-176.
-
(2013)
Onco Targets Ther
, vol.6
, pp. 161-176
-
-
D'Cruz, O.J.1
Uckun, F.M.2
-
9
-
-
84879748062
-
Targeting BTK with ibrutinib in relapsed chronic lymphocytic leukemia
-
Byrd JC, Furman RR, Coutre SE, Flinn IW, Burger JA, Blum KA et al. Targeting BTK with ibrutinib in relapsed chronic lymphocytic leukemia. N Engl J Med 2013; 369: 32-42.
-
(2013)
N Engl J Med
, 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
-
10
-
-
84881225049
-
Targeting BTK with ibrutinib in relapsed or refractory mantle-cell lymphoma
-
Wang ML, Rule S, Martin P, Goy A, Auer R, Kahl BS et al. Targeting BTK with ibrutinib in relapsed or refractory mantle-cell lymphoma. N Engl J Med 2013; 369: 507-516.
-
(2013)
N Engl J Med
, 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
-
11
-
-
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 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
-
12
-
-
84883160397
-
Ibrutinib and novel BTK inhibitors in clinical development
-
Akinleye A, Chen Y, Mukhi N, Song Y, Liu D. Ibrutinib and novel BTK inhibitors in clinical development. J Hematol Oncol 2013; 6: 59.
-
(2013)
J Hematol Oncol
, vol.6
, pp. 59
-
-
Akinleye, A.1
Chen, Y.2
Mukhi, N.3
Song, Y.4
Liu, D.5
-
13
-
-
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
-
14
-
-
84899624581
-
MAP kinaseinteracting kinases-emerging targets against cancer
-
Diab S, Kumarasiri M, Yu M, Teo T, Proud C, Milne R et al. MAP kinaseinteracting kinases-emerging targets against cancer. Chem Biol 2014; 21: 441-452.
-
(2014)
Chem Biol
, vol.21
, pp. 441-452
-
-
Diab, S.1
Kumarasiri, M.2
Yu, M.3
Teo, T.4
Proud, C.5
Milne, R.6
-
15
-
-
0025314596
-
Malignant transformation by a eukaryotic initiation factor subunit that binds to mRNA 5' cap
-
Lazaris-Karatzas A, Montine KS, Sonenberg N. Malignant transformation by a eukaryotic initiation factor subunit that binds to mRNA 5' cap. Nature 1990; 345: 544-547.
-
(1990)
Nature
, vol.345
, pp. 544-547
-
-
Lazaris-Karatzas, A.1
Montine, K.S.2
Sonenberg, N.3
-
16
-
-
34250755685
-
Epigenetic activation of a subset of mRNAs by eIF4E explains its effects on cell proliferation
-
Mamane Y, Petroulakis E, Martineau Y, Sato TA, Larsson O, Rajasekhar VK et al. Epigenetic activation of a subset of mRNAs by eIF4E explains its effects on cell proliferation. PLoS One 2007; 2: e242.
-
(2007)
PLoS One
, vol.2
, pp. e242
-
-
Mamane, Y.1
Petroulakis, E.2
Martineau, Y.3
Sato, T.A.4
Larsson, O.5
Rajasekhar, V.K.6
-
17
-
-
38849180436
-
Targeting the eukaryotic translation initiation factor 4E for cancer therapy
-
Graff JR, Konicek BW, Carter JH, Marcusson EG. Targeting the eukaryotic translation initiation factor 4E for cancer therapy. Cancer Res 2008; 68: 631-634.
-
(2008)
Cancer Res
, vol.68
, pp. 631-634
-
-
Graff, J.R.1
Konicek, B.W.2
Carter, J.H.3
Marcusson, E.G.4
-
18
-
-
2442648845
-
The translation factor eIF-4E promotes tumor formation and cooperates with c-Myc in lymphomagenesis
-
Ruggero D, Montanaro L, Ma L, Xu W, Londei P, Cordon-Cardo C et al. The translation factor eIF-4E promotes tumor formation and cooperates with c-Myc in lymphomagenesis. Nat Med 2004; 10: 484-486.
-
(2004)
Nat Med
, vol.10
, pp. 484-486
-
-
Ruggero, D.1
Montanaro, L.2
Ma, L.3
Xu, W.4
Londei, P.5
Cordon-Cardo, C.6
-
20
-
-
79952223149
-
Therapeutic inhibition of MAP kinase interacting kinase blocks eukaryotic initiation factor 4E phosphorylation and suppresses outgrowth of experimental lung metastases
-
Konicek BW, Stephens JR, McNulty AM, Robichaud N, Peery RB, Dumstorf CA et al. Therapeutic inhibition of MAP kinase interacting kinase blocks eukaryotic initiation factor 4E phosphorylation and suppresses outgrowth of experimental lung metastases. Cancer Res 2011; 71: 1849-1857.
-
(2011)
Cancer Res
, vol.71
, pp. 1849-1857
-
-
Konicek, B.W.1
Stephens, J.R.2
McNulty, A.M.3
Robichaud, N.4
Peery, R.B.5
Dumstorf, C.A.6
-
21
-
-
84879720960
-
Inhibition of Mnk kinase activity by cercosporamide and suppressive effects on acute myeloid leukemia precursors
-
Altman JK, Szilard A, Konicek BW, Iversen PW, Kroczynska B, Glaser H et al. Inhibition of Mnk kinase activity by cercosporamide and suppressive effects on acute myeloid leukemia precursors. Blood 2013; 121: 3675-3681.
-
(2013)
Blood
, vol.121
, pp. 3675-3681
-
-
Altman, J.K.1
Szilard, A.2
Konicek, B.W.3
Iversen, P.W.4
Kroczynska, B.5
Glaser, H.6
-
22
-
-
84875055944
-
The Bruton tyrosine kinase (BTK) inhibitor PCI-32765 synergistically increases proteasome inhibitor activity in diffuse large-B cell lymphoma (DLBCL) and mantle cell lymphoma (MCL) cells sensitive or resistant to bortezomib
-
Dasmahapatra G, Patel H, Dent P, Fisher RI, Friedberg J, Grant S. The Bruton tyrosine kinase (BTK) inhibitor PCI-32765 synergistically increases proteasome inhibitor activity in diffuse large-B cell lymphoma (DLBCL) and mantle cell lymphoma (MCL) cells sensitive or resistant to bortezomib. Br J Haematol 2013; 161: 43-56.
-
(2013)
Br J Haematol
, vol.161
, pp. 43-56
-
-
Dasmahapatra, G.1
Patel, H.2
Dent, P.3
Fisher, R.I.4
Friedberg, J.5
Grant, S.6
-
23
-
-
53549085163
-
Inhibition of polysome assembly enhances imatinib activity against chronic myelogenous leukemia and overcomes imatinib resistance
-
Zhang M, Fu W, Prabhu S, Moore JC, Ko J, Kim JW et al. Inhibition of polysome assembly enhances imatinib activity against chronic myelogenous leukemia and overcomes imatinib resistance. Mol Cell Biol 2008; 28: 6496-6509.
-
(2008)
Mol Cell Biol
, vol.28
, pp. 6496-6509
-
-
Zhang, M.1
Fu, W.2
Prabhu, S.3
Moore, J.C.4
Ko, J.5
Kim, J.W.6
-
24
-
-
72949092456
-
Novel mutant-selective EGFR kinase inhibitors against EGFR T790M
-
Zhou W, Ercan D, Chen L, Yun CH, Li D, Capelletti M et al. 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
-
25
-
-
33745933955
-
HKL-3000: The integration of data reduction and structure solution-from diffraction images to an initial model in minutes
-
Minor W, Cymborowski M, Otwinowski Z, Chruszcz M. HKL-3000: the integration of data reduction and structure solution-from diffraction images to an initial model in minutes. Acta Crystallogr D Biol Crystallogr 2006; 62: 859-866.
-
(2006)
Acta Crystallogr D Biol Crystallogr
, vol.62
, pp. 859-866
-
-
Minor, W.1
Cymborowski, M.2
Otwinowski, Z.3
Chruszcz, M.4
-
26
-
-
76449098262
-
PHENIX: A comprehensive Python-based system for macromolecular structure solution
-
Adams PD, Afonine PV, Bunkoczi G, Chen VB, Davis IW, Echols N et al. PHENIX: a comprehensive Python-based system for macromolecular structure solution. Acta Crystallogr D Biol Crystallogr 2010; 66: 213-221.
-
(2010)
Acta Crystallogr D Biol Crystallogr
, vol.66
, pp. 213-221
-
-
Adams, P.D.1
Afonine, P.V.2
Bunkoczi, G.3
Chen, V.B.4
Davis, I.W.5
Echols, N.6
-
28
-
-
7544226311
-
PRODRG: A tool for high-throughput crystallography of protein-ligand complexes
-
Schuttelkopf AW, van Aalten DM. PRODRG: a tool for high-throughput crystallography of protein-ligand complexes. Acta Crystallogr D Biol Crystallogr 2004; 60: 1355-1363.
-
(2004)
Acta Crystallogr D Biol Crystallogr
, vol.60
, pp. 1355-1363
-
-
Schuttelkopf, A.W.1
Van Aalten, D.M.2
-
29
-
-
38049084406
-
Discovery of selective irreversible inhibitors for Bruton's tyrosine kinase
-
Pan Z, Scheerens H, Li SJ, Schultz BE, Sprengeler PA, Burrill LC et al. Discovery of selective irreversible inhibitors for Bruton's tyrosine kinase. Chem Med Chem 2007; 2: 58-61.
-
(2007)
Chem Med Chem
, 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
-
30
-
-
84880447005
-
Inhibition of Btk with CC-292 provides early pharmacodynamic assessment of activity in mice and humans
-
Evans EK, Tester R, Aslanian S, Karp R, Sheets M, Labenski MT et al. Inhibition of Btk with CC-292 provides early pharmacodynamic assessment of activity in mice and humans. J Pharmacol Exp Ther 2013; 346: 219-228.
-
(2013)
J Pharmacol Exp Ther
, vol.346
, pp. 219-228
-
-
Evans, E.K.1
Tester, R.2
Aslanian, S.3
Karp, R.4
Sheets, M.5
Labenski, M.T.6
-
31
-
-
26444592983
-
Crystal structures of the Mnk2 kinase domain reveal an inhibitory conformation and a zinc binding site
-
Jauch R, Jakel S, Netter C, Schreiter K, Aicher B, Jackle H et al. Crystal structures of the Mnk2 kinase domain reveal an inhibitory conformation and a zinc binding site. Structure 2005; 13: 1559-1568.
-
(2005)
Structure
, vol.13
, pp. 1559-1568
-
-
Jauch, R.1
Jakel, S.2
Netter, C.3
Schreiter, K.4
Aicher, B.5
Jackle, H.6
-
32
-
-
79952265072
-
Discovery of 9-(6-aminopyridin-3-yl)-1-(3-(trifluoromethyl)phenyl)benzo[h][1,6]naphthyridin-2 (1H)-one (Torin2) as a potent, selective, and orally available mammalian target of rapamycin (mTOR) inhibitor for treatment of cancer
-
Liu Q, Wang J, Kang SA, Thoreen CC, Hur W, Ahmed T et al. Discovery of 9-(6-aminopyridin-3-yl)-1-(3-(trifluoromethyl)phenyl)benzo[h][1,6]naphthyridin-2 (1H)-one (Torin2) as a potent, selective, and orally available mammalian target of rapamycin (mTOR) inhibitor for treatment of cancer. J Med Chem 2011; 54: 1473-1480.
-
(2011)
J Med Chem
, vol.54
, pp. 1473-1480
-
-
Liu, Q.1
Wang, J.2
Kang, S.A.3
Thoreen, C.C.4
Hur, W.5
Ahmed, T.6
-
33
-
-
19744365702
-
A small molecule-kinase interaction map for clinical kinase inhibitors
-
Fabian MA, Biggs WH 3rd, Treiber DK, Atteridge CE, Azimioara MD, Benedetti MG et al. A small molecule-kinase interaction map for clinical kinase inhibitors. Nat Biotechnol 2005; 23: 329-336.
-
(2005)
Nat Biotechnol
, vol.23
, pp. 329-336
-
-
Fabian, M.A.1
Biggs, W.H.2
Treiber, D.K.3
Atteridge, C.E.4
Azimioara, M.D.5
Benedetti, M.G.6
-
34
-
-
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 et al. The Bruton tyrosine kinase inhibitor PCI-32765 blocks B-cell activation and is efficacious in models of autoimmune disease and B-cell malignancy. Proc Natl Acad Sci USA 2010; 107: 13075-13080.
-
(2010)
Proc Natl Acad Sci USA
, 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
-
35
-
-
84880532700
-
Discovery of a selective irreversible BMX inhibitor for prostate cancer
-
Liu F, Zhang X, Weisberg E, Chen S, Hur W, Wu H et al. Discovery of a selective irreversible BMX inhibitor for prostate cancer. ACS Chem Biol 2013; 8: 1423-1428.
-
(2013)
ACS Chem Biol
, vol.8
, pp. 1423-1428
-
-
Liu, F.1
Zhang, X.2
Weisberg, E.3
Chen, S.4
Hur, W.5
Wu, H.6
-
36
-
-
84894095058
-
Adaptation to mTOR kinase inhibitors by amplification of eIF4E to maintain cap-dependent translation
-
Cope CL, Gilley R, Balmanno K, Sale MJ, Howarth KD, Hampson M et al. Adaptation to mTOR kinase inhibitors by amplification of eIF4E to maintain cap-dependent translation. J Cell Sci 2014; 127: 788-800.
-
(2014)
J Cell Sci
, vol.127
, pp. 788-800
-
-
Cope, C.L.1
Gilley, R.2
Balmanno, K.3
Sale, M.J.4
Howarth, K.D.5
Hampson, M.6
-
37
-
-
84881478230
-
Rapamycin enhances eIF4E phosphorylation by activating MAP kinase-interacting kinase 2a (Mnk2a)
-
Stead RL, Proud CG. Rapamycin enhances eIF4E phosphorylation by activating MAP kinase-interacting kinase 2a (Mnk2a). FEBS Lett 2013; 587: 2623-2628.
-
(2013)
FEBS Lett
, vol.587
, pp. 2623-2628
-
-
Stead, R.L.1
Proud, C.G.2
-
38
-
-
84893801239
-
Combinatorial drug screening identifies synergistic co-targeting of Bruton's tyrosine kinase and the proteasome in mantle cell lymphoma
-
Axelrod M, Ou Z, Brett LK, Zhang L, Lopez ER, Tamayo AT et al. Combinatorial drug screening identifies synergistic co-targeting of Bruton's tyrosine kinase and the proteasome in mantle cell lymphoma. Leukemia 2014; 28: 407-410.
-
(2014)
Leukemia
, vol.28
, pp. 407-410
-
-
Axelrod, M.1
Ou, Z.2
Brett, L.K.3
Zhang, L.4
Lopez, E.R.5
Tamayo, A.T.6
-
39
-
-
78049457409
-
Utilizing targeted cancer therapeutic agents in combination: Novel approaches and urgent requirements
-
Kummar S, Chen HX, Wright J, Holbeck S, Millin MD, Tomaszewski J et al. Utilizing targeted cancer therapeutic agents in combination: novel approaches and urgent requirements. Nat Rev Drug Discov 2010; 9: 843-856.
-
(2010)
Nat Rev Drug Discov
, vol.9
, pp. 843-856
-
-
Kummar, S.1
Chen, H.X.2
Wright, J.3
Holbeck, S.4
Millin, M.D.5
Tomaszewski, J.6
-
40
-
-
3242794178
-
From magic bullets to designed multiple ligands
-
Morphy R, Kay C, Rankovic Z. From magic bullets to designed multiple ligands. Drug Discov Today 2004; 9: 641-651.
-
(2004)
Drug Discov Today
, vol.9
, pp. 641-651
-
-
Morphy, R.1
Kay, C.2
Rankovic, Z.3
-
41
-
-
47349124275
-
What does systems biology mean for drug development
-
Schrattenholz A, Soskic V. What does systems biology mean for drug development Curr Med Chem 2008; 15: 1520-1528.
-
(2008)
Curr Med Chem
, vol.15
, pp. 1520-1528
-
-
Schrattenholz, A.1
Soskic, V.2
-
42
-
-
54249155522
-
Network pharmacology: The next paradigm in drug discovery
-
Hopkins AL. Network pharmacology: the next paradigm in drug discovery. Nat Chem Biol 2008; 4: 682-690.
-
(2008)
Nat Chem Biol
, vol.4
, pp. 682-690
-
-
Hopkins, A.L.1
|