-
1
-
-
0036527429
-
Protein kinases-the major drug targets of the twenty-first century?
-
Cohen P. Protein kinases-the major drug targets of the twenty-first century?. Nat Rev Drug Discov 2002, 1:309-315.
-
(2002)
Nat Rev Drug Discov
, vol.1
, pp. 309-315
-
-
Cohen, P.1
-
3
-
-
0034306450
-
Specificity and mechanism of action of some commonly used protein kinase inhibitors
-
Davies S.P., Reddy H., Caivano M., Cohen P. Specificity and mechanism of action of some commonly used protein kinase inhibitors. Biochem J 2000, 351:95-105.
-
(2000)
Biochem J
, vol.351
, pp. 95-105
-
-
Davies, S.P.1
Reddy, H.2
Caivano, M.3
Cohen, P.4
-
4
-
-
57749188299
-
Targeting cancer with small molecule kinase inhibitors
-
Zhang J., Yang P.L., Gray N.S. Targeting cancer with small molecule kinase inhibitors. Nat Rev Cancer 2009, 9:28-39.
-
(2009)
Nat Rev Cancer
, vol.9
, pp. 28-39
-
-
Zhang, J.1
Yang, P.L.2
Gray, N.S.3
-
5
-
-
33745298429
-
Rational design of inhibitors that bind to inactive kinase conformations
-
Liu Y., Gray N.S. Rational design of inhibitors that bind to inactive kinase conformations. Nat Chem Biol 2006, 2:358-364.
-
(2006)
Nat Chem Biol
, vol.2
, pp. 358-364
-
-
Liu, Y.1
Gray, N.S.2
-
6
-
-
77950573400
-
Through the " gatekeeper door" : exploiting the active kinase conformation
-
Zuccotto F., Ardini E., Casale E., Angiolini M. Through the " gatekeeper door" : exploiting the active kinase conformation. J Med Chem 2010, 53:2681-2694.
-
(2010)
J Med Chem
, vol.53
, pp. 2681-2694
-
-
Zuccotto, F.1
Ardini, E.2
Casale, E.3
Angiolini, M.4
-
7
-
-
38049018155
-
A quantitative analysis of kinase inhibitor selectivity
-
Karaman M.W., Herrgard S., Treiber D.K., et al. A quantitative analysis of kinase inhibitor selectivity. Nat Biotechnol 2008, 26:127-132.
-
(2008)
Nat Biotechnol
, vol.26
, pp. 127-132
-
-
Karaman, M.W.1
Herrgard, S.2
Treiber, D.K.3
-
8
-
-
42949150113
-
High-throughput kinase profiling as a platform for drug discovery
-
Goldstien D.M., Gray N.S., Zarrinkar P.P. High-throughput kinase profiling as a platform for drug discovery. Nat Rev Drug Discov 2008, 7:391-397.
-
(2008)
Nat Rev Drug Discov
, vol.7
, pp. 391-397
-
-
Goldstien, D.M.1
Gray, N.S.2
Zarrinkar, P.P.3
-
9
-
-
45949106612
-
The challenge of selecting protein kinase assays for lead discovery optimization
-
Ma H., Deacon S., Horiuchi K. The challenge of selecting protein kinase assays for lead discovery optimization. Expert Opin Drug Dis 2008, 3:607-621.
-
(2008)
Expert Opin Drug Dis
, vol.3
, pp. 607-621
-
-
Ma, H.1
Deacon, S.2
Horiuchi, K.3
-
10
-
-
58849089632
-
High-throughput biochemical kinase selectivity assays: Panel development and screening
-
Card A., Caldwell C., Min H., et al. High-throughput biochemical kinase selectivity assays: Panel development and screening. J Biomol Screen 2009, 14:31-42.
-
(2009)
J Biomol Screen
, vol.14
, pp. 31-42
-
-
Card, A.1
Caldwell, C.2
Min, H.3
-
11
-
-
41249099841
-
Efficacy of TG101348, a selective JAK2 inhibitor, in treatment of a murine model of JAK2V617F-induced polycythemia vera
-
Wernig G., Kharas M.G., Okabe R., et al. Efficacy of TG101348, a selective JAK2 inhibitor, in treatment of a murine model of JAK2V617F-induced polycythemia vera. Cancer Cell 2008, 13:311-320.
-
(2008)
Cancer Cell
, vol.13
, pp. 311-320
-
-
Wernig, G.1
Kharas, M.G.2
Okabe, R.3
-
12
-
-
77950684805
-
Preclinical characterization of the selective JAK1/2 inhibitor INCB018424: therapeutic implications for the treatment of myeloproliferative neoplasms
-
Quintás-Cardama A., Vaddi K., Liu P., et al. Preclinical characterization of the selective JAK1/2 inhibitor INCB018424: therapeutic implications for the treatment of myeloproliferative neoplasms. Blood 2010, 115:3109-3117.
-
(2010)
Blood
, vol.115
, pp. 3109-3117
-
-
Quintás-Cardama, A.1
Vaddi, K.2
Liu, P.3
-
14
-
-
77951517669
-
Advances in the discovery of small molecule JAK3 inhibitors
-
San Diego: Academic Press, J.E. Macor (Ed.)
-
Wrobleski S.T., Pitts W.J. Advances in the discovery of small molecule JAK3 inhibitors. Annual reports in medicinal chemistry volume 44 2009, 247-264. San Diego: Academic Press. J.E. Macor (Ed.).
-
(2009)
Annual reports in medicinal chemistry volume 44
, pp. 247-264
-
-
Wrobleski, S.T.1
Pitts, W.J.2
-
15
-
-
47249157224
-
Therapeutic targeting of Janus kinases
-
Pesu M., Laurence A., Kishore N., et al. Therapeutic targeting of Janus kinases. Immunol Rev 2008, 223:132-142.
-
(2008)
Immunol Rev
, vol.223
, pp. 132-142
-
-
Pesu, M.1
Laurence, A.2
Kishore, N.3
-
16
-
-
0032076183
-
Disruption of the Jak1 gene demonstrates obligatory and nonredundant roles of the Jaks in cytokine-induced biologic responses
-
Rodig S.J., Meraz M.A., White J.M., et al. Disruption of the Jak1 gene demonstrates obligatory and nonredundant roles of the Jaks in cytokine-induced biologic responses. Cell 1998, 93:373-383.
-
(1998)
Cell
, vol.93
, pp. 373-383
-
-
Rodig, S.J.1
Meraz, M.A.2
White, J.M.3
-
17
-
-
18244432009
-
Jak2 deficiency defines an essential developmental checkpoint in definitive hematopoiesis
-
Neubauer H., Cumano A., Müller M., et al. Jak2 deficiency defines an essential developmental checkpoint in definitive hematopoiesis. Cell 1998, 93:397-409.
-
(1998)
Cell
, vol.93
, pp. 397-409
-
-
Neubauer, H.1
Cumano, A.2
Müller, M.3
-
18
-
-
0032076542
-
Jak2 is essential for signaling through a variety of cytokine receptors
-
Parganas E., Wang D., Stravopodis D., et al. Jak2 is essential for signaling through a variety of cytokine receptors. Cell 1998, 93:385-395.
-
(1998)
Cell
, vol.93
, pp. 385-395
-
-
Parganas, E.1
Wang, D.2
Stravopodis, D.3
-
19
-
-
0028799457
-
Defects in B lymphocyte maturation and T lymphocyte activation in mice lacking Jak3
-
Thomis D.C., Gurniak C.B., Tivol E., et al. Defects in B lymphocyte maturation and T lymphocyte activation in mice lacking Jak3. Science 1995, 270:794-797.
-
(1995)
Science
, vol.270
, pp. 794-797
-
-
Thomis, D.C.1
Gurniak, C.B.2
Tivol, E.3
-
20
-
-
0028840706
-
Defective lymphoid development in mice lacking Jak3
-
Nosaka T., van Deursen J.M.A., Tripp R.A., et al. Defective lymphoid development in mice lacking Jak3. Science 1995, 270:800-802.
-
(1995)
Science
, vol.270
, pp. 800-802
-
-
Nosaka, T.1
van Deursen, J.M.A.2
Tripp, R.A.3
-
21
-
-
0033696404
-
Partial impairment of cytokine responses in Tyk2-deficient mice
-
Karaghiosoff M., Neubauer H., Lassnig C., et al. Partial impairment of cytokine responses in Tyk2-deficient mice. Immunity 2000, 13:549-560.
-
(2000)
Immunity
, vol.13
, pp. 549-560
-
-
Karaghiosoff, M.1
Neubauer, H.2
Lassnig, C.3
-
22
-
-
15244349726
-
TYK2 is a key regulator of the surveillance of B lymphoid tumors
-
Stoiber D., Kovacic B., Schuster C., et al. TYK2 is a key regulator of the surveillance of B lymphoid tumors. J Clin Invest 2004, 114:1650-1658.
-
(2004)
J Clin Invest
, vol.114
, pp. 1650-1658
-
-
Stoiber, D.1
Kovacic, B.2
Schuster, C.3
-
23
-
-
52949127317
-
The JAK kinases: not just another kinase drug discovery target
-
Wilks A.F. The JAK kinases: not just another kinase drug discovery target. Semin Cell Dev Biol 2008, 19:319-328.
-
(2008)
Semin Cell Dev Biol
, vol.19
, pp. 319-328
-
-
Wilks, A.F.1
-
24
-
-
68749084623
-
CYT387, a selective JAK1/JAK2 inhibitor: in vitro assessment of kinase selectivity and preclinical studies using cell lines and primary cells from polycythemia vera patients
-
Pardanani A., Lasho T., Smith G., et al. CYT387, a selective JAK1/JAK2 inhibitor: in vitro assessment of kinase selectivity and preclinical studies using cell lines and primary cells from polycythemia vera patients. Leukemia 2009, 23:1441-1445.
-
(2009)
Leukemia
, vol.23
, pp. 1441-1445
-
-
Pardanani, A.1
Lasho, T.2
Smith, G.3
-
25
-
-
33845360035
-
Ba/F3 cells and their use in kinase drug discovery
-
Warmuth M., Kim S., Gu X.J., et al. Ba/F3 cells and their use in kinase drug discovery. Curr Opin Oncol 2007, 19:55-60.
-
(2007)
Curr Opin Oncol
, vol.19
, pp. 55-60
-
-
Warmuth, M.1
Kim, S.2
Gu, X.J.3
-
26
-
-
0034653478
-
Transforming properties of chimeric TEL-JAK proteins in Ba/F3 cells
-
Lacronique V., Boureux A., Monni R., et al. Transforming properties of chimeric TEL-JAK proteins in Ba/F3 cells. Blood 2000, 95:2076-2083.
-
(2000)
Blood
, vol.95
, pp. 2076-2083
-
-
Lacronique, V.1
Boureux, A.2
Monni, R.3
-
27
-
-
33645322121
-
Robust regression for high throughput drug screening
-
Fomenko I., Durst M., Balaban D. Robust regression for high throughput drug screening. Comput Meth Prog Bio 2006, 82:31-37.
-
(2006)
Comput Meth Prog Bio
, vol.82
, pp. 31-37
-
-
Fomenko, I.1
Durst, M.2
Balaban, D.3
-
28
-
-
78650362917
-
Discovery of CP-690,550: a potent and selective janus kinase (JAK) inhibitor for the treatment of autoimmune disease and organ transplant rejection
-
Flanagan M.E., Blumenkopf T.A., Brissette W.H., et al. Discovery of CP-690,550: a potent and selective janus kinase (JAK) inhibitor for the treatment of autoimmune disease and organ transplant rejection. J Med Chem 2010, 53:8468-8484.
-
(2010)
J Med Chem
, vol.53
, pp. 8468-8484
-
-
Flanagan, M.E.1
Blumenkopf, T.A.2
Brissette, W.H.3
-
29
-
-
77954581104
-
Kinetic study of human full-length wild-type JAK2 and V617F mutant proteins
-
Erdman D., Allard B., Bohn J., et al. Kinetic study of human full-length wild-type JAK2 and V617F mutant proteins. Open Enzyme Inhibition J 2008, 1:80-84.
-
(2008)
Open Enzyme Inhibition J
, vol.1
, pp. 80-84
-
-
Erdman, D.1
Allard, B.2
Bohn, J.3
-
30
-
-
24944497371
-
Features of selective kinase inhibitors
-
Knight Z.A., Shokat K.M. Features of selective kinase inhibitors. Chem Biol 2005, 12:621-637.
-
(2005)
Chem Biol
, vol.12
, pp. 621-637
-
-
Knight, Z.A.1
Shokat, K.M.2
-
31
-
-
84055211821
-
Discovery of potent and highly selective thienopyridine Janus kinase 2 inhibitors
-
Schenkel L.B., Huang X., Cheng A., et al. Discovery of potent and highly selective thienopyridine Janus kinase 2 inhibitors. J Med Chem 2011, 54:8440-8450.
-
(2011)
J Med Chem
, vol.54
, pp. 8440-8450
-
-
Schenkel, L.B.1
Huang, X.2
Cheng, A.3
-
32
-
-
84858855487
-
JAK inhibitors for myeloproliferative neoplasms: clarifying facts from myths
-
Tefferi A. JAK inhibitors for myeloproliferative neoplasms: clarifying facts from myths. Blood 2012, 119:2721-2730.
-
(2012)
Blood
, vol.119
, pp. 2721-2730
-
-
Tefferi, A.1
|