-
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? Nature Rev. Drug Discovery 2002, 1 (4) 309-315
-
(2002)
Nature Rev. Drug Discovery
, vol.1
, Issue.4
, pp. 309-315
-
-
Cohen, P.1
-
2
-
-
0037032835
-
The protein kinase complement of the human genome
-
Manning, G.; Whyte, D.; Martinez, R.; Hunter, T.; Sudarsanam, S. The protein kinase complement of the human genome Science (New York, N.Y.) 2002, 298 (5600) 1912-1934
-
(2002)
Science (New York, N.Y.)
, vol.298
, Issue.5600
, pp. 1912-1934
-
-
Manning, G.1
Whyte, D.2
Martinez, R.3
Hunter, T.4
Sudarsanam, S.5
-
3
-
-
33947101019
-
Patterns of somatic mutation in human cancer genomes
-
Greenman, C.; Stephens, P.; Smith, R.; Dalgliesh, G.; Hunter, C.; Bignell, G.; Davies, H.; Teague, J.; Butler, A.; Stevens, C.; Edkins, S.; O'Meara, S.; Vastrik, I.; Schmidt, E.; Avis, T.; Barthorpe, S.; Bhamra, G.; Buck, G.; Choudhury, B.; Clements, J.; Cole, J.; Dicks, E.; Forbes, S.; Gray, K.; Halliday, K.; Harrison, R.; Hills, K.; Hinton, J.; Jenkinson, A.; Jones, D.; Menzies, A.; Mironenko, T.; Perry, J.; Raine, K.; Richardson, D.; Shepherd, R.; Small, A.; Tofts, C.; Varian, J.; Webb, T.; West, S.; Widaa, S.; Yates, A.; Cahill, D.; Louis, D.; Goldstraw, P.; Nicholson, A.; Brasseur, F.; Looijenga, L.; Weber, B.; Chiew, Y.-E.; DeFazio, A.; Greaves, M.; Green, A.; Campbell, P.; Birney, E.; Easton, D.; Chenevix-Trench, G.; Tan, M.-H.; Khoo, S.; Teh, B.; Yuen, S.; Leung, S.; Wooster, R.; Futreal, P.; Stratton, M. Patterns of somatic mutation in human cancer genomes Nature 2007, 446 (7132) 153-158
-
(2007)
Nature
, vol.446
, Issue.7132
, pp. 153-158
-
-
Greenman, C.1
Stephens, P.2
Smith, R.3
Dalgliesh, G.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.14
Avis, T.15
Barthorpe, S.16
Bhamra, G.17
Buck, G.18
Choudhury, B.19
Clements, J.20
Cole, J.21
Dicks, E.22
Forbes, S.23
Gray, K.24
Halliday, K.25
Harrison, R.26
Hills, K.27
Hinton, J.28
Jenkinson, A.29
Jones, D.30
Menzies, A.31
Mironenko, T.32
Perry, J.33
Raine, K.34
Richardson, D.35
Shepherd, R.36
Small, A.37
Tofts, C.38
Varian, J.39
Webb, T.40
West, S.41
Widaa, S.42
Yates, A.43
Cahill, D.44
Louis, D.45
Goldstraw, P.46
Nicholson, A.47
Brasseur, F.48
Looijenga, L.49
Weber, B.50
Chiew, Y.-E.51
Defazio, A.52
Greaves, M.53
Green, A.54
Campbell, P.55
Birney, E.56
Easton, D.57
Chenevix-Trench, G.58
Tan, M.-H.59
Khoo, S.60
Teh, B.61
Yuen, S.62
Leung, S.63
Wooster, R.64
Futreal, P.65
Stratton, M.66
more..
-
4
-
-
38049018155
-
A quantitative analysis of kinase inhibitor selectivity
-
Karaman, M.; Herrgard, S.; Treiber, D.; Gallant, P.; Atteridge, C.; Campbell, B.; Chan, K.; Ciceri, P.; Davis, M.; Edeen, P.; Faraoni, R.; Floyd, M.; Hunt, J.; Lockhart, D.; Milanov, Z.; Morrison, M.; Pallares, G.; Patel, H.; Pritchard, S.; Wodicka, L.; Zarrinkar, P. A quantitative analysis of kinase inhibitor selectivity Nat. Biotechnol. 2008, 26 (1) 127-132
-
(2008)
Nat. Biotechnol.
, vol.26
, Issue.1
, pp. 127-132
-
-
Karaman, M.1
Herrgard, S.2
Treiber, D.3
Gallant, P.4
Atteridge, C.5
Campbell, B.6
Chan, K.7
Ciceri, P.8
Davis, M.9
Edeen, P.10
Faraoni, R.11
Floyd, M.12
Hunt, J.13
Lockhart, D.14
Milanov, Z.15
Morrison, M.16
Pallares, G.17
Patel, H.18
Pritchard, S.19
Wodicka, L.20
Zarrinkar, P.21
more..
-
5
-
-
77950473958
-
Kinase selectivity potential for inhibitors targeting the ATP binding site: a network analysis
-
Huang, D.; Zhou, T.; Lafleur, K.; Nevado, C.; Caflisch, A. Kinase selectivity potential for inhibitors targeting the ATP binding site: a network analysis Bioinformatics (Oxford, England) 2009, 26 (2) 198-204
-
(2009)
Bioinformatics (Oxford, England)
, vol.26
, Issue.2
, pp. 198-204
-
-
Huang, D.1
Zhou, T.2
Lafleur, K.3
Nevado, C.4
Caflisch, A.5
-
6
-
-
80755125575
-
Comprehensive analysis of kinase inhibitor selectivity
-
Davis, M.; Hunt, J.; Herrgard, S.; Ciceri, P.; Wodicka, L.; Pallares, G.; Hocker, M.; Treiber, D.; Zarrinkar, P. Comprehensive analysis of kinase inhibitor selectivity Nature Biotechnol. 2011, 29 (11) 1046-1051
-
(2011)
Nature Biotechnol.
, vol.29
, Issue.11
, pp. 1046-1051
-
-
Davis, M.1
Hunt, J.2
Herrgard, S.3
Ciceri, P.4
Wodicka, L.5
Pallares, G.6
Hocker, M.7
Treiber, D.8
Zarrinkar, P.9
-
7
-
-
77649204688
-
Selectively nonselective kinase inhibition: striking the right balance
-
Morphy, R. Selectively nonselective kinase inhibition: striking the right balance J. Med. Chem. 2010, 53 (4) 1413-1437
-
(2010)
J. Med. Chem.
, vol.53
, Issue.4
, pp. 1413-1437
-
-
Morphy, R.1
-
8
-
-
4344668661
-
Drug repositioning: identifying and developing new uses for existing drugs
-
Ashburn, T.; Thor, K. Drug repositioning: identifying and developing new uses for existing drugs Nature Rev. Drug Discovery 2004, 3 (8) 673-683
-
(2004)
Nature Rev. Drug Discovery
, vol.3
, Issue.8
, pp. 673-683
-
-
Ashburn, T.1
Thor, K.2
-
9
-
-
84864952187
-
Predicting new indications for approved drugs using a proteochemometric method
-
Dakshanamurthy, S.; Issa, N.; Assefnia, S.; Seshasayee, A.; Peters, O.; Madhavan, S.; Uren, A.; Brown, M.; Byers, S. Predicting new indications for approved drugs using a proteochemometric method J. Med. Chem. 2012, 55 (15) 6832-6848
-
(2012)
J. Med. Chem.
, vol.55
, Issue.15
, pp. 6832-6848
-
-
Dakshanamurthy, S.1
Issa, N.2
Assefnia, S.3
Seshasayee, A.4
Peters, O.5
Madhavan, S.6
Uren, A.7
Brown, M.8
Byers, S.9
-
10
-
-
84861490509
-
Modern phenotypic drug discovery is a viable, neoclassic pharma strategy
-
Lee, J.; Uhlik, M.; Moxham, C.; Tomandl, D.; Sall, D. Modern phenotypic drug discovery is a viable, neoclassic pharma strategy J. Med. Chem. 2012, 55 (10) 4527-4538
-
(2012)
J. Med. Chem.
, vol.55
, Issue.10
, pp. 4527-4538
-
-
Lee, J.1
Uhlik, M.2
Moxham, C.3
Tomandl, D.4
Sall, D.5
-
11
-
-
84886953565
-
Phenotypic screens as a renewed approach for drug discovery
-
Zheng, W.; Thorne, N.; McKew, J. Phenotypic screens as a renewed approach for drug discovery Drug Discovery Today 2013, 18 (21-22) 1067-73
-
(2013)
Drug Discovery Today
, vol.18
, Issue.2122
, pp. 1067-1073
-
-
Zheng, W.1
Thorne, N.2
McKew, J.3
-
12
-
-
84905496728
-
Phenotypic screening in cancer drug discovery - past, present and future
-
Moffat, J. G.; Rudolph, J.; Bailey, D. Phenotypic screening in cancer drug discovery-past, present and future Nature Rev. Drug Discovery 2014, 13 (8) 588-602
-
(2014)
Nature Rev. Drug Discovery
, vol.13
, Issue.8
, pp. 588-602
-
-
Moffat, J.G.1
Rudolph, J.2
Bailey, D.3
-
13
-
-
35748983210
-
Target deconvolution strategies in drug discovery
-
Terstappen, G.; Schlüpen, C.; Raggiaschi, R.; Gaviraghi, G. Target deconvolution strategies in drug discovery Nature Rev. Drug Discovery 2007, 6 (11) 891-903
-
(2007)
Nature Rev. Drug Discovery
, vol.6
, Issue.11
, pp. 891-903
-
-
Terstappen, G.1
Schlüpen, C.2
Raggiaschi, R.3
Gaviraghi, G.4
-
14
-
-
84874630073
-
Target Identification for Small Bioactive Molecules: Finding the Needle in the Haystack
-
Ziegler, S.; Pries, V.; Hedberg, C.; Waldmann, H. Target Identification for Small Bioactive Molecules: Finding the Needle in the Haystack Angew. Chem., Int. Ed. Engl. 2013, 52, 2744-2792
-
(2013)
Angew. Chem., Int. Ed. Engl.
, vol.52
, pp. 2744-2792
-
-
Ziegler, S.1
Pries, V.2
Hedberg, C.3
Waldmann, H.4
-
15
-
-
84863772301
-
The Kinome and its Impact on Medicinal Chemistry
-
Drewry, D. H.; Bamborough, P.; Schneider, K.; Smith, G. K. The Kinome and its Impact on Medicinal Chemistry Kinase Drug Discovery 2012, 1-29
-
(2012)
Kinase Drug Discovery
, pp. 1-29
-
-
Drewry, D.H.1
Bamborough, P.2
Schneider, K.3
Smith, G.K.4
-
16
-
-
84875619719
-
A broad activity screen in support of a chemogenomic map for kinase signalling research and drug discovery
-
Gao, Y.; Davies, S.; Augustin, M.; Woodward, A.; Patel, U.; Kovelman, R.; Harvey, K. A broad activity screen in support of a chemogenomic map for kinase signalling research and drug discovery Biochem. J. 2013, 451 (2) 313-328
-
(2013)
Biochem. J.
, vol.451
, Issue.2
, pp. 313-328
-
-
Gao, Y.1
Davies, S.2
Augustin, M.3
Woodward, A.4
Patel, U.5
Kovelman, R.6
Harvey, K.7
-
17
-
-
84856392676
-
Mass spectrometry-based proteomics in preclinical drug discovery
-
Schirle, M.; Bantscheff, M.; Kuster, B. Mass spectrometry-based proteomics in preclinical drug discovery Chemistry & biology 2012, 19 (1) 72-84
-
(2012)
Chemistry & biology
, vol.19
, Issue.1
, pp. 72-84
-
-
Schirle, M.1
Bantscheff, M.2
Kuster, B.3
-
18
-
-
69249136243
-
Target profiling of small molecules by chemical proteomics
-
Rix, U.; Superti-Furga, G. Target profiling of small molecules by chemical proteomics Nat. Chem. Biol. 2009, 5 (9) 616-624
-
(2009)
Nat. Chem. Biol.
, vol.5
, Issue.9
, pp. 616-624
-
-
Rix, U.1
Superti-Furga, G.2
-
19
-
-
84979524500
-
Global discovery of protein kinases and other nucleotide-binding proteins by mass spectrometry
-
Xiao, Y.; Wang, Y., Global discovery of protein kinases and other nucleotide-binding proteins by mass spectrometry. Mass Spectrom Rev., DOI: 10.1002/mas.21447.
-
Mass Spectrom Rev.
-
-
Xiao, Y.1
Wang, Y.2
-
20
-
-
37049014938
-
Chemical proteomic profiles of the BCR-ABL inhibitors imatinib, nilotinib, and dasatinib reveal novel kinase and nonkinase targets
-
Rix, U.; Hantschel, O.; Dürnberger, G.; Remsing Rix, L.; Planyavsky, M.; Fernbach, N.; Kaupe, I.; Bennett, K.; Valent, P.; Colinge, J.; Köcher, T.; Superti-Furga, G. Chemical proteomic profiles of the BCR-ABL inhibitors imatinib, nilotinib, and dasatinib reveal novel kinase and nonkinase targets Blood 2007, 110 (12) 4055-4063
-
(2007)
Blood
, vol.110
, Issue.12
, pp. 4055-4063
-
-
Rix, U.1
Hantschel, O.2
Dürnberger, G.3
Remsing Rix, L.4
Planyavsky, M.5
Fernbach, N.6
Kaupe, I.7
Bennett, K.8
Valent, P.9
Colinge, J.10
Köcher, T.11
Superti-Furga, G.12
-
21
-
-
74249085402
-
A comprehensive target selectivity survey of the BCR-ABL kinase inhibitor INNO-406 by kinase profiling and chemical proteomics in chronic myeloid leukemia cells
-
Rix, U.; Remsing Rix, L.; Terker, A.; Fernbach, N.; Hantschel, O.; Planyavsky, M.; Breitwieser, F.; Herrmann, H.; Colinge, J.; Bennett, K.; Augustin, M.; Till, J.; Heinrich, M.; Valent, P.; Superti-Furga, G. A comprehensive target selectivity survey of the BCR-ABL kinase inhibitor INNO-406 by kinase profiling and chemical proteomics in chronic myeloid leukemia cells Leukemia 2010, 24 (1) 44-50
-
(2010)
Leukemia
, vol.24
, Issue.1
, pp. 44-50
-
-
Rix, U.1
Remsing Rix, L.2
Terker, A.3
Fernbach, N.4
Hantschel, O.5
Planyavsky, M.6
Breitwieser, F.7
Herrmann, H.8
Colinge, J.9
Bennett, K.10
Augustin, M.11
Till, J.12
Heinrich, M.13
Valent, P.14
Superti-Furga, G.15
-
22
-
-
63849172494
-
Identifying the proteins to which small-molecule probes and drugs bind in cells
-
Ong, S. E.; Schenone, M.; Margolin, A. A.; Li, X.; Do, K.; Doud, M. K.; Mani, D. R.; Kuai, L.; Wang, X.; Wood, J. L.; Tolliday, N. J.; Koehler, A. N.; Marcaurelle, L. A.; Golub, T. R.; Gould, R. J.; Schreiber, S. L.; Carr, S. A. Identifying the proteins to which small-molecule probes and drugs bind in cells Proc. Natl. Acad. Sci. U. S. A. 2009, 106 (12) 4617-22
-
(2009)
Proc. Natl. Acad. Sci. U. S. A.
, vol.106
, Issue.12
, pp. 4617-4622
-
-
Ong, S.E.1
Schenone, M.2
Margolin, A.A.3
Li, X.4
Do, K.5
Doud, M.K.6
Mani, D.R.7
Kuai, L.8
Wang, X.9
Wood, J.L.10
Tolliday, N.J.11
Koehler, A.N.12
Marcaurelle, L.A.13
Golub, T.R.14
Gould, R.J.15
Schreiber, S.L.16
Carr, S.A.17
-
23
-
-
79959493188
-
In situ kinase profiling reveals functionally relevant properties of native kinases
-
Patricelli, M.; Nomanbhoy, T.; Wu, J.; Brown, H.; Zhou, D.; Zhang, J.; Jagannathan, S.; Aban, A.; Okerberg, E.; Herring, C.; Nordin, B.; Weissig, H.; Yang, Q.; Lee, J.-D.; Gray, N.; Kozarich, J. In situ kinase profiling reveals functionally relevant properties of native kinases Chem. Biol. 2011, 18 (6) 699-710
-
(2011)
Chem. Biol.
, vol.18
, Issue.6
, pp. 699-710
-
-
Patricelli, M.1
Nomanbhoy, T.2
Wu, J.3
Brown, H.4
Zhou, D.5
Zhang, J.6
Jagannathan, S.7
Aban, A.8
Okerberg, E.9
Herring, C.10
Nordin, B.11
Weissig, H.12
Yang, Q.13
Lee, J.-D.14
Gray, N.15
Kozarich, J.16
-
24
-
-
84898751411
-
A Targeted Quantitative Proteomics Strategy for Global Kinome Profiling of Cancer Cells and Tissues
-
Xiao, Y.; Guo, L.; Wang, Y. A Targeted Quantitative Proteomics Strategy for Global Kinome Profiling of Cancer Cells and Tissues Mol. Cell Proteomics 2014, 13 (4) 1065-75
-
(2014)
Mol. Cell Proteomics
, vol.13
, Issue.4
, pp. 1065-1075
-
-
Xiao, Y.1
Guo, L.2
Wang, Y.3
-
25
-
-
34948875686
-
Quantitative chemical proteomics reveals mechanisms of action of clinical ABL kinase inhibitors
-
Bantscheff, M.; Eberhard, D.; Abraham, Y.; Bastuck, S.; Boesche, M.; Hobson, S.; Mathieson, T.; Perrin, J.; Raida, M.; Rau, C.; Reader, V. r.; Sweetman, G.; Bauer, A.; Bouwmeester, T.; Hopf, C.; Kruse, U.; Neubauer, G.; Ramsden, N.; Rick, J.; Kuster, B.; Drewes, G. Quantitative chemical proteomics reveals mechanisms of action of clinical ABL kinase inhibitors Nature Biotechnol. 2007, 25 (9) 1035-1044
-
(2007)
Nature Biotechnol.
, vol.25
, Issue.9
, pp. 1035-1044
-
-
Bantscheff, M.1
Eberhard, D.2
Abraham, Y.3
Bastuck, S.4
Boesche, M.5
Hobson, S.6
Mathieson, T.7
Perrin, J.8
Raida, M.9
Rau, C.10
Reader, V.R.11
Sweetman, G.12
Bauer, A.13
Bouwmeester, T.14
Hopf, C.15
Kruse, U.16
Neubauer, G.17
Ramsden, N.18
Rick, J.19
Kuster, B.20
Drewes, G.21
more..
-
26
-
-
84875914218
-
Comparing Immobilized Kinase Inhibitors and Covalent ATP Probes for Proteomic Profiling of Kinase Expression and Drug Selectivity
-
Lemeer, S.; Zörgiebel, C.; Ruprecht, B.; Kohl, K.; Kuster, B. Comparing Immobilized Kinase Inhibitors and Covalent ATP Probes for Proteomic Profiling of Kinase Expression and Drug Selectivity J. Proteome Res. 2013, 12 (4) 1723-1731
-
(2013)
J. Proteome Res.
, vol.12
, Issue.4
, pp. 1723-1731
-
-
Lemeer, S.1
Zörgiebel, C.2
Ruprecht, B.3
Kohl, K.4
Kuster, B.5
-
27
-
-
84859765844
-
Dynamic reprogramming of the kinome in response to targeted MEK inhibition in triple-negative breast cancer
-
Duncan, J.; Whittle, M.; Nakamura, K.; Abell, A.; Midland, A.; Zawistowski, J.; Johnson, N.; Granger, D.; Jordan, N.; Darr, D.; Usary, J.; Kuan, P.-F.; Smalley, D.; Major, B.; He, X.; Hoadley, K.; Zhou, B.; Sharpless, N.; Perou, C.; Kim, W.; Gomez, S.; Chen, X.; Jin, J.; Frye, S.; Earp, H.; Graves, L.; Johnson, G. Dynamic reprogramming of the kinome in response to targeted MEK inhibition in triple-negative breast cancer Cell 2012, 149 (2) 307-321
-
(2012)
Cell
, vol.149
, Issue.2
, pp. 307-321
-
-
Duncan, J.1
Whittle, M.2
Nakamura, K.3
Abell, A.4
Midland, A.5
Zawistowski, J.6
Johnson, N.7
Granger, D.8
Jordan, N.9
Darr, D.10
Usary, J.11
Kuan, P.-F.12
Smalley, D.13
Major, B.14
He, X.15
Hoadley, K.16
Zhou, B.17
Sharpless, N.18
Perou, C.19
Kim, W.20
Gomez, S.21
Chen, X.22
Jin, J.23
Frye, S.24
Earp, H.25
Graves, L.26
Johnson, G.27
more..
-
28
-
-
84879907745
-
Characterization of the novel broad-spectrum kinase inhibitor CTx-0294885 as an affinity reagent for mass spectrometry-based kinome profiling
-
Zhang, L.; Holmes, I.; Hochgräfe, F.; Walker, S.; Ali, N.; Humphrey, E.; Wu, J.; de Silva, M.; Kersten, W.; Connor, T.; Falk, H.; Allan, L.; Street, I.; Bentley, J.; Pilling, P.; Monahan, B.; Peat, T.; Daly, R. Characterization of the novel broad-spectrum kinase inhibitor CTx-0294885 as an affinity reagent for mass spectrometry-based kinome profiling J. Proteome Res. 2013, 12 (7) 3104-3116
-
(2013)
J. Proteome Res.
, vol.12
, Issue.7
, pp. 3104-3116
-
-
Zhang, L.1
Holmes, I.2
Hochgräfe, F.3
Walker, S.4
Ali, N.5
Humphrey, E.6
Wu, J.7
De Silva, M.8
Kersten, W.9
Connor, T.10
Falk, H.11
Allan, L.12
Street, I.13
Bentley, J.14
Pilling, P.15
Monahan, B.16
Peat, T.17
Daly, R.18
-
29
-
-
84865576726
-
Quantitative mass spectrometry in proteomics: critical review update from 2007 to the present
-
Bantscheff, M.; Lemeer, S.; Savitski, M.; Kuster, B. Quantitative mass spectrometry in proteomics: critical review update from 2007 to the present Anal. Bioanal. Chem. 2012, 404 (4) 939-965
-
(2012)
Anal. Bioanal. Chem.
, vol.404
, Issue.4
, pp. 939-965
-
-
Bantscheff, M.1
Lemeer, S.2
Savitski, M.3
Kuster, B.4
-
30
-
-
84871312669
-
A public-private partnership to unlock the untargeted kinome
-
Knapp, S.; Arruda, P.; Blagg, J.; Burley, S.; Drewry, D.; Edwards, A.; Fabbro, D.; Gillespie, P.; Gray, N.; Kuster, B.; Lackey, K.; Mazzafera, P.; Tomkinson, N.; Willson, T.; Workman, P.; Zuercher, W. A public-private partnership to unlock the untargeted kinome Nat. Chem. Biol. 2013, 9 (1) 3-6
-
(2013)
Nat. Chem. Biol.
, vol.9
, Issue.1
, pp. 3-6
-
-
Knapp, S.1
Arruda, P.2
Blagg, J.3
Burley, S.4
Drewry, D.5
Edwards, A.6
Fabbro, D.7
Gillespie, P.8
Gray, N.9
Kuster, B.10
Lackey, K.11
Mazzafera, P.12
Tomkinson, N.13
Willson, T.14
Workman, P.15
Zuercher, W.16
-
31
-
-
70549086229
-
Large-scale proteomics analysis of the human kinome
-
Oppermann, F. S.; Gnad, F.; Olsen, J. V.; Hornberger, R.; Greff, Z.; Keri, G.; Mann, M.; Daub, H. Large-scale proteomics analysis of the human kinome Mol. Cell Proteomics 2009, 8 (7) 1751-64
-
(2009)
Mol. Cell Proteomics
, vol.8
, Issue.7
, pp. 1751-1764
-
-
Oppermann, F.S.1
Gnad, F.2
Olsen, J.V.3
Hornberger, R.4
Greff, Z.5
Keri, G.6
Mann, M.7
Daub, H.8
-
32
-
-
80555144285
-
Kinase inhibitor profiling using chemoproteomics
-
Schirle, M.; Petrella, E.; Brittain, S.; Schwalb, D.; Harrington, E.; Cornella-Taracido, I.; Tallarico, J. Kinase inhibitor profiling using chemoproteomics Methods Mol. Biol. (Clifton, N.J.) 2012, 795, 161-177
-
(2012)
Methods Mol. Biol. (Clifton, N.J.)
, vol.795
, pp. 161-177
-
-
Schirle, M.1
Petrella, E.2
Brittain, S.3
Schwalb, D.4
Harrington, E.5
Cornella-Taracido, I.6
Tallarico, J.7
-
33
-
-
84881159771
-
Characterization of a Chemical Affinity Probe Targeting Akt Kinases
-
Pachl, F.; Plattner, P.; Ruprecht, B.; Médard, G.; Sewald, N.; Kuster, B. Characterization of a Chemical Affinity Probe Targeting Akt Kinases J. Proteome Res. 2013, 12, 3792-3800
-
(2013)
J. Proteome Res.
, vol.12
, pp. 3792-3800
-
-
Pachl, F.1
Plattner, P.2
Ruprecht, B.3
Médard, G.4
Sewald, N.5
Kuster, B.6
-
34
-
-
84899863913
-
New Affinity Probe Targeting VEGF Receptors for Kinase Inhibitor Selectivity Profiling by Chemical Proteomics
-
Ku, X.; Heinzlmeir, S.; Helm, D.; Médard, G.; Kuster, B. New Affinity Probe Targeting VEGF Receptors for Kinase Inhibitor Selectivity Profiling by Chemical Proteomics J. Proteome Res. 2014, 13 (5) 2445-2452
-
(2014)
J. Proteome Res.
, vol.13
, Issue.5
, pp. 2445-2452
-
-
Ku, X.1
Heinzlmeir, S.2
Helm, D.3
Médard, G.4
Kuster, B.5
-
35
-
-
84881613658
-
Global Proteome Analysis of the NCI-60 Cell Line Panel
-
Gholami, A.; Hahne, H.; Wu, Z.; Auer, F.; Meng, C.; Wilhelm, M.; Kuster, B. Global Proteome Analysis of the NCI-60 Cell Line Panel Cell Rep. 2013, 4 (3) 609-620
-
(2013)
Cell Rep.
, vol.4
, Issue.3
, pp. 609-620
-
-
Gholami, A.1
Hahne, H.2
Wu, Z.3
Auer, F.4
Meng, C.5
Wilhelm, M.6
Kuster, B.7
-
36
-
-
84924382604
-
-
https://github.com/ThomasKuehne/kinaseblender.
-
-
-
-
37
-
-
0032977124
-
Frequent co-alterations of TP53, p16/CDKN2A, p14ARF, PTEN tumor suppressor genes in human glioma cell lines
-
Ishii, N.; Maier, D.; Merlo, A.; Tada, M.; Sawamura, Y.; Diserens, A. C.; Van Meir, E. G. Frequent co-alterations of TP53, p16/CDKN2A, p14ARF, PTEN tumor suppressor genes in human glioma cell lines Brain Pathol. 1999, 9 (3) 469-79
-
(1999)
Brain Pathol.
, vol.9
, Issue.3
, pp. 469-479
-
-
Ishii, N.1
Maier, D.2
Merlo, A.3
Tada, M.4
Sawamura, Y.5
Diserens, A.C.6
Van Meir, E.G.7
-
38
-
-
84888093389
-
A new chemical probe for quantitative proteomic profiling of fibroblast growth factor receptor and its inhibitors
-
Ku, X.; Heinzlmeir, S.; Liu, X.; Médard, G.; Kuster, B. A new chemical probe for quantitative proteomic profiling of fibroblast growth factor receptor and its inhibitors J. Proteomics 2014, 96 (16) 44-55
-
(2014)
J. Proteomics
, vol.96
, Issue.16
, pp. 44-55
-
-
Ku, X.1
Heinzlmeir, S.2
Liu, X.3
Médard, G.4
Kuster, B.5
-
39
-
-
84884903629
-
DMSO enhances electrospray response, boosting sensitivity of proteomic experiments
-
Hahne, H.; Pachl, F.; Ruprecht, B.; Maier, S.; Klaeger, S.; Helm, D.; Médard, G.; Wilm, M.; Lemeer, S.; Kuster, B. DMSO enhances electrospray response, boosting sensitivity of proteomic experiments Nat. Methods 2013, 10, 989-991
-
(2013)
Nat. Methods
, vol.10
, pp. 989-991
-
-
Hahne, H.1
Pachl, F.2
Ruprecht, B.3
Maier, S.4
Klaeger, S.5
Helm, D.6
Médard, G.7
Wilm, M.8
Lemeer, S.9
Kuster, B.10
-
40
-
-
57449099865
-
MaxQuant enables high peptide identification rates, individualized p.p.b.-range mass accuracies and proteome-wide protein quantification
-
Cox, J.; Mann, M. MaxQuant enables high peptide identification rates, individualized p.p.b.-range mass accuracies and proteome-wide protein quantification Nat. Biotechnol. 2008, 26 (12) 1367-72
-
(2008)
Nat. Biotechnol.
, vol.26
, Issue.12
, pp. 1367-1372
-
-
Cox, J.1
Mann, M.2
-
41
-
-
84907197082
-
Accurate proteome-wide label-free quantification by delayed normalization and maximal peptide ratio extraction, termed MaxLFQ
-
Cox, J.; Hein, M. Y.; Luber, C. A.; Paron, I.; Nagaraj, N.; Mann, M. Accurate proteome-wide label-free quantification by delayed normalization and maximal peptide ratio extraction, termed MaxLFQ Mol. Cell Proteomics 2014, 13 (9) 2513-26
-
(2014)
Mol. Cell Proteomics
, vol.13
, Issue.9
, pp. 2513-2526
-
-
Cox, J.1
Hein, M.Y.2
Luber, C.A.3
Paron, I.4
Nagaraj, N.5
Mann, M.6
-
42
-
-
70349624519
-
Proteomics strategy for quantitative protein interaction profiling in cell extracts
-
Sharma, K.; Weber, C.; Bairlein, M.; Greff, Z.; Kéri, G.; Cox, J.; Olsen, J.; Daub, H. Proteomics strategy for quantitative protein interaction profiling in cell extracts Nat. Methods 2009, 6 (10) 741-744
-
(2009)
Nat. Methods
, vol.6
, Issue.10
, pp. 741-744
-
-
Sharma, K.1
Weber, C.2
Bairlein, M.3
Greff, Z.4
Kéri, G.5
Cox, J.6
Olsen, J.7
Daub, H.8
-
43
-
-
19744365702
-
A small molecule-kinase interaction map for clinical kinase inhibitors
-
Fabian, M.; Biggs, W.; Treiber, D.; Atteridge, C.; Azimioara, M.; Benedetti, M.; Carter, T.; Ciceri, P.; Edeen, P.; Floyd, M.; Ford, J.; Galvin, M.; Gerlach, J.; Grotzfeld, R.; Herrgard, S.; Insko, D.; Insko, M.; Lai, A.; Lélias, J.-M.; Mehta, S.; Milanov, Z.; Velasco, A.; Wodicka, L.; Patel, H.; Zarrinkar, P.; Lockhart, D. A small molecule-kinase interaction map for clinical kinase inhibitors Nature Biotechnol. 2005, 23 (3) 329-336
-
(2005)
Nature Biotechnol.
, vol.23
, Issue.3
, pp. 329-336
-
-
Fabian, M.1
Biggs, W.2
Treiber, D.3
Atteridge, C.4
Azimioara, M.5
Benedetti, M.6
Carter, T.7
Ciceri, P.8
Edeen, P.9
Floyd, M.10
Ford, J.11
Galvin, M.12
Gerlach, J.13
Grotzfeld, R.14
Herrgard, S.15
Insko, D.16
Insko, M.17
Lai, A.18
Lélias, J.-M.19
Mehta, S.20
Milanov, Z.21
Velasco, A.22
Wodicka, L.23
Patel, H.24
Zarrinkar, P.25
Lockhart, D.26
more..
-
44
-
-
0037194619
-
Discovery of aminothiazole inhibitors of cyclin-dependent kinase 2: synthesis, X-ray crystallographic analysis, and biological activities
-
Kim, K. S.; Kimball, S. D.; Misra, R. N.; Rawlins, D. B.; Hunt, J. T.; Xiao, H. Y.; Lu, S.; Qian, L.; Han, W. C.; Shan, W.; Mitt, T.; Cai, Z. W.; Poss, M. A.; Zhu, H.; Sack, J. S.; Tokarski, J. S.; Chang, C. Y.; Pavletich, N.; Kamath, A.; Humphreys, W. G.; Marathe, P.; Bursuker, I.; Kellar, K. A.; Roongta, U.; Batorsky, R.; Mulheron, J. G.; Bol, D.; Fairchild, C. R.; Lee, F. Y.; Webster, K. R. Discovery of aminothiazole inhibitors of cyclin-dependent kinase 2: synthesis, X-ray crystallographic analysis, and biological activities J. Med. Chem. 2002, 45 (18) 3905-27
-
(2002)
J. Med. Chem.
, vol.45
, Issue.18
, pp. 3905-3927
-
-
Kim, K.S.1
Kimball, S.D.2
Misra, R.N.3
Rawlins, D.B.4
Hunt, J.T.5
Xiao, H.Y.6
Lu, S.7
Qian, L.8
Han, W.C.9
Shan, W.10
Mitt, T.11
Cai, Z.W.12
Poss, M.A.13
Zhu, H.14
Sack, J.S.15
Tokarski, J.S.16
Chang, C.Y.17
Pavletich, N.18
Kamath, A.19
Humphreys, W.G.20
Marathe, P.21
Bursuker, I.22
Kellar, K.A.23
Roongta, U.24
Batorsky, R.25
Mulheron, J.G.26
Bol, D.27
Fairchild, C.R.28
Lee, F.Y.29
Webster, K.R.30
more..
-
45
-
-
13444311605
-
Crystal structure of a human cyclin-dependent kinase 6 complex with a flavonol inhibitor, fisetin
-
Lu, H.; Chang, D. J.; Baratte, B.; Meijer, L.; Schulze-Gahmen, U. Crystal structure of a human cyclin-dependent kinase 6 complex with a flavonol inhibitor, fisetin J. Med. Chem. 2005, 48 (3) 737-43
-
(2005)
J. Med. Chem.
, vol.48
, Issue.3
, pp. 737-743
-
-
Lu, H.1
Chang, D.J.2
Baratte, B.3
Meijer, L.4
Schulze-Gahmen, U.5
-
46
-
-
84899619048
-
Stereospecific targeting of MTH1 by (S)-crizotinib as an anticancer strategy
-
Huber, K. V.; Salah, E.; Radic, B.; Gridling, M.; Elkins, J. M.; Stukalov, A.; Jemth, A. S.; Gokturk, C.; Sanjiv, K.; Stromberg, K.; Pham, T.; Berglund, U. W.; Colinge, J.; Bennett, K. L.; Loizou, J. I.; Helleday, T.; Knapp, S.; Superti-Furga, G. Stereospecific targeting of MTH1 by (S)-crizotinib as an anticancer strategy Nature 2014, 508 (7495) 222-7
-
(2014)
Nature
, vol.508
, Issue.7495
, pp. 222-227
-
-
Huber, K.V.1
Salah, E.2
Radic, B.3
Gridling, M.4
Elkins, J.M.5
Stukalov, A.6
Jemth, A.S.7
Gokturk, C.8
Sanjiv, K.9
Stromberg, K.10
Pham, T.11
Berglund, U.W.12
Colinge, J.13
Bennett, K.L.14
Loizou, J.I.15
Helleday, T.16
Knapp, S.17
Superti-Furga, G.18
-
47
-
-
80755125565
-
Comprehensive assay of kinase catalytic activity reveals features of kinase inhibitor selectivity
-
Anastassiadis, T.; Deacon, S.; Devarajan, K.; Ma, H.; Peterson, J. Comprehensive assay of kinase catalytic activity reveals features of kinase inhibitor selectivity Nature Biotechnol. 2011, 29 (11) 1039-1045
-
(2011)
Nature Biotechnol.
, vol.29
, Issue.11
, pp. 1039-1045
-
-
Anastassiadis, T.1
Deacon, S.2
Devarajan, K.3
Ma, H.4
Peterson, J.5
-
48
-
-
84873056956
-
Activity-based kinase profiling of approved tyrosine kinase inhibitors
-
Kitagawa, D.; Yokota, K.; Gouda, M.; Narumi, Y.; Ohmoto, H.; Nishiwaki, E.; Akita, K.; Kirii, Y. Activity-based kinase profiling of approved tyrosine kinase inhibitors Genes Cells 2013, 18 (2) 110-22
-
(2013)
Genes Cells
, vol.18
, Issue.2
, pp. 110-122
-
-
Kitagawa, D.1
Yokota, K.2
Gouda, M.3
Narumi, Y.4
Ohmoto, H.5
Nishiwaki, E.6
Akita, K.7
Kirii, Y.8
-
49
-
-
84857422382
-
Testing the promiscuity of commercial kinase inhibitors against the AGC kinase group using a split-luciferase screen
-
Jester, B.; Gaj, A.; Shomin, C.; Cox, K.; Ghosh, I. Testing the promiscuity of commercial kinase inhibitors against the AGC kinase group using a split-luciferase screen J. Med. Chem. 2012, 55 (4) 1526-1537
-
(2012)
J. Med. Chem.
, vol.55
, Issue.4
, pp. 1526-1537
-
-
Jester, B.1
Gaj, A.2
Shomin, C.3
Cox, K.4
Ghosh, I.5
-
50
-
-
77249114233
-
Hit to lead account of the discovery of bisbenzamide and related ureidobenzamide inhibitors of Rho kinase
-
Morwick, T.; Buttner, F. H.; Cywin, C. L.; Dahmann, G.; Hickey, E.; Jakes, S.; Kaplita, P.; Kashem, M. A.; Kerr, S.; Kugler, S.; Mao, W.; Marshall, D.; Paw, Z.; Shih, C. K.; Wu, F.; Young, E. Hit to lead account of the discovery of bisbenzamide and related ureidobenzamide inhibitors of Rho kinase J. Med. Chem. 2010, 53 (2) 759-77
-
(2010)
J. Med. Chem.
, vol.53
, Issue.2
, pp. 759-777
-
-
Morwick, T.1
Buttner, F.H.2
Cywin, C.L.3
Dahmann, G.4
Hickey, E.5
Jakes, S.6
Kaplita, P.7
Kashem, M.A.8
Kerr, S.9
Kugler, S.10
Mao, W.11
Marshall, D.12
Paw, Z.13
Shih, C.K.14
Wu, F.15
Young, E.16
-
51
-
-
77953287632
-
Substituted 2H-isoquinolin-1-one as potent Rho-Kinase inhibitors. Part 1: Hit-to-lead account
-
Wu, F.; Buttner, F. H.; Chen, R.; Hickey, E.; Jakes, S.; Kaplita, P.; Kashem, M. A.; Kerr, S.; Kugler, S.; Paw, Z.; Prokopowicz, A.; Shih, C. K.; Snow, R.; Young, E.; Cywin, C. L. Substituted 2H-isoquinolin-1-one as potent Rho-Kinase inhibitors. Part 1: Hit-to-lead account Bioorg. Med. Chem. Lett. 2010, 20 (11) 3235-9
-
(2010)
Bioorg. Med. Chem. Lett.
, vol.20
, Issue.11
, pp. 3235-3239
-
-
Wu, F.1
Buttner, F.H.2
Chen, R.3
Hickey, E.4
Jakes, S.5
Kaplita, P.6
Kashem, M.A.7
Kerr, S.8
Kugler, S.9
Paw, Z.10
Prokopowicz, A.11
Shih, C.K.12
Snow, R.13
Young, E.14
Cywin, C.L.15
-
52
-
-
0030656619
-
Calcium sensitization of smooth muscle mediated by a Rho-associated protein kinase in hypertension
-
Uehata, M.; Ishizaki, T.; Satoh, H.; Ono, T.; Kawahara, T.; Morishita, T.; Tamakawa, H.; Yamagami, K.; Inui, J.; Maekawa, M.; Narumiya, S. Calcium sensitization of smooth muscle mediated by a Rho-associated protein kinase in hypertension Nature 1997, 389 (6654) 990-4
-
(1997)
Nature
, vol.389
, Issue.6654
, pp. 990-994
-
-
Uehata, M.1
Ishizaki, T.2
Satoh, H.3
Ono, T.4
Kawahara, T.5
Morishita, T.6
Tamakawa, H.7
Yamagami, K.8
Inui, J.9
Maekawa, M.10
Narumiya, S.11
-
53
-
-
26444518165
-
Inhibition of Rho kinase (ROCK) leads to increased cerebral blood flow and stroke protection
-
Rikitake, Y.; Kim, H. H.; Huang, Z.; Seto, M.; Yano, K.; Asano, T.; Moskowitz, M. A.; Liao, J. K. Inhibition of Rho kinase (ROCK) leads to increased cerebral blood flow and stroke protection Stroke 2005, 36 (10) 2251-7
-
(2005)
Stroke
, vol.36
, Issue.10
, pp. 2251-2257
-
-
Rikitake, Y.1
Kim, H.H.2
Huang, Z.3
Seto, M.4
Yano, K.5
Asano, T.6
Moskowitz, M.A.7
Liao, J.K.8
-
54
-
-
33644857442
-
The structure of dimeric ROCK I reveals the mechanism for ligand selectivity
-
Jacobs, M.; Hayakawa, K.; Swenson, L.; Bellon, S.; Fleming, M.; Taslimi, P.; Doran, J. The structure of dimeric ROCK I reveals the mechanism for ligand selectivity J. Biol. Chem. 2006, 281 (1) 260-8
-
(2006)
J. Biol. Chem.
, vol.281
, Issue.1
, pp. 260-268
-
-
Jacobs, M.1
Hayakawa, K.2
Swenson, L.3
Bellon, S.4
Fleming, M.5
Taslimi, P.6
Doran, J.7
-
55
-
-
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, L. A.; Smith, A. M.; Sirisawad, M.; Verner, E.; Loury, D.; Chang, B.; Li, S.; Pan, Z.; Thamm, D. H.; Miller, R. A.; Buggy, J. J. 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. U. S. A. 2010, 107 (29) 13075-80
-
(2010)
Proc. Natl. Acad. Sci. U. S. A.
, vol.107
, Issue.29
, 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
-
56
-
-
12244301581
-
In vivo antitumor activity of SU11248, a novel tyrosine kinase inhibitor targeting vascular endothelial growth factor and platelet-derived growth factor receptors: determination of a pharmacokinetic/pharmacodynamic relationship
-
Mendel, D. B.; Laird, A. D.; Xin, X.; Louie, S. G.; Christensen, J. G.; Li, G.; Schreck, R. E.; Abrams, T. J.; Ngai, T. J.; Lee, L. B.; Murray, L. J.; Carver, J.; Chan, E.; Moss, K. G.; Haznedar, J. O.; Sukbuntherng, J.; Blake, R. A.; Sun, L.; Tang, C.; Miller, T.; Shirazian, S.; McMahon, G.; Cherrington, J. M. In vivo antitumor activity of SU11248, a novel tyrosine kinase inhibitor targeting vascular endothelial growth factor and platelet-derived growth factor receptors: determination of a pharmacokinetic/pharmacodynamic relationship Clin. Cancer Res. 2003, 9 (1) 327-37
-
(2003)
Clin. Cancer Res.
, vol.9
, Issue.1
, pp. 327-337
-
-
Mendel, D.B.1
Laird, A.D.2
Xin, X.3
Louie, S.G.4
Christensen, J.G.5
Li, G.6
Schreck, R.E.7
Abrams, T.J.8
Ngai, T.J.9
Lee, L.B.10
Murray, L.J.11
Carver, J.12
Chan, E.13
Moss, K.G.14
Haznedar, J.O.15
Sukbuntherng, J.16
Blake, R.A.17
Sun, L.18
Tang, C.19
Miller, T.20
Shirazian, S.21
Mcmahon, G.22
Cherrington, J.M.23
more..
-
57
-
-
80052806086
-
Structure based drug design of crizotinib (PF-02341066), a potent and selective dual inhibitor of mesenchymal-epithelial transition factor (c-MET) kinase and anaplastic lymphoma kinase (ALK)
-
Cui, J. J.; Tran-Dubé, M.; Shen, H.; Nambu, M.; Kung, P. P.; Pairish, M.; Jia, L.; Meng, J.; Funk, L.; Botrous, I.; McTigue, M.; Grodsky, N.; Ryan, K.; Padrique, E.; Alton, G.; Timofeevski, S.; Yamazaki, S.; Li, Q.; Zou, H.; Christensen, J.; Mroczkowski, B.; Bender, S.; Kania, R. S.; Edwards, M. P. Structure based drug design of crizotinib (PF-02341066), a potent and selective dual inhibitor of mesenchymal-epithelial transition factor (c-MET) kinase and anaplastic lymphoma kinase (ALK) J. Med. Chem. 2011, 54 (18) 6342-63
-
(2011)
J. Med. Chem.
, vol.54
, Issue.18
, pp. 6342-6363
-
-
Cui, J.J.1
Tran-Dubé, M.2
Shen, H.3
Nambu, M.4
Kung, P.P.5
Pairish, M.6
Jia, L.7
Meng, J.8
Funk, L.9
Botrous, I.10
Mctigue, M.11
Grodsky, N.12
Ryan, K.13
Padrique, E.14
Alton, G.15
Timofeevski, S.16
Yamazaki, S.17
Li, Q.18
Zou, H.19
Christensen, J.20
Mroczkowski, B.21
Bender, S.22
Kania, R.S.23
Edwards, M.P.24
more..
-
58
-
-
84864621502
-
Identification of regulators of polyploidization presents therapeutic targets for treatment of AMKL
-
Wen, Q.; Goldenson, B.; Silver, S. J.; Schenone, M.; Dancik, V.; Huang, Z.; Wang, L. Z.; Lewis, T. A.; An, W. F.; Li, X.; Bray, M. A.; Thiollier, C.; Diebold, L.; Gilles, L.; Vokes, M. S.; Moore, C. B.; Bliss-Moreau, M.; Verplank, L.; Tolliday, N. J.; Mishra, R.; Vemula, S.; Shi, J.; Wei, L.; Kapur, R.; Lopez, C. K.; Gerby, B.; Ballerini, P.; Pflumio, F.; Gilliland, D. G.; Goldberg, L.; Birger, Y.; Izraeli, S.; Gamis, A. S.; Smith, F. O.; Woods, W. G.; Taub, J.; Scherer, C. A.; Bradner, J. E.; Goh, B. C.; Mercher, T.; Carpenter, A. E.; Gould, R. J.; Clemons, P. A.; Carr, S. A.; Root, D. E.; Schreiber, S. L.; Stern, A. M.; Crispino, J. D. Identification of regulators of polyploidization presents therapeutic targets for treatment of AMKL Cell 2012, 150 (3) 575-89
-
(2012)
Cell
, vol.150
, Issue.3
, pp. 575-589
-
-
Wen, Q.1
Goldenson, B.2
Silver, S.J.3
Schenone, M.4
Dancik, V.5
Huang, Z.6
Wang, L.Z.7
Lewis, T.A.8
An, W.F.9
Li, X.10
Bray, M.A.11
Thiollier, C.12
Diebold, L.13
Gilles, L.14
Vokes, M.S.15
Moore, C.B.16
Bliss-Moreau, M.17
Verplank, L.18
Tolliday, N.J.19
Mishra, R.20
Vemula, S.21
Shi, J.22
Wei, L.23
Kapur, R.24
Lopez, C.K.25
Gerby, B.26
Ballerini, P.27
Pflumio, F.28
Gilliland, D.G.29
Goldberg, L.30
Birger, Y.31
Izraeli, S.32
Gamis, A.S.33
Smith, F.O.34
Woods, W.G.35
Taub, J.36
Scherer, C.A.37
Bradner, J.E.38
Goh, B.C.39
Mercher, T.40
Carpenter, A.E.41
Gould, R.J.42
Clemons, P.A.43
Carr, S.A.44
Root, D.E.45
Schreiber, S.L.46
Stern, A.M.47
Crispino, J.D.48
more..
-
59
-
-
0035838950
-
Pharmacological profile of hydroxy fasudil as a selective rho kinase inhibitor on ischemic brain damage
-
Satoh, S.; Utsunomiya, T.; Tsurui, K.; Kobayashi, T.; Ikegaki, I.; Sasaki, Y.; Asano, T. Pharmacological profile of hydroxy fasudil as a selective rho kinase inhibitor on ischemic brain damage Life Sci. 2001, 69 (12) 1441-53
-
(2001)
Life Sci.
, vol.69
, Issue.12
, pp. 1441-1453
-
-
Satoh, S.1
Utsunomiya, T.2
Tsurui, K.3
Kobayashi, T.4
Ikegaki, I.5
Sasaki, Y.6
Asano, T.7
-
60
-
-
0026534605
-
Effect of AT877 on cerebral vasospasm after aneurysmal subarachnoid hemorrhage. Results of a prospective placebo-controlled double-blind trial
-
Shibuya, M.; Suzuki, Y.; Sugita, K.; Saito, I.; Sasaki, T.; Takakura, K.; Nagata, I.; Kikuchi, H.; Takemae, T.; Hidaka, H. Effect of AT877 on cerebral vasospasm after aneurysmal subarachnoid hemorrhage. Results of a prospective placebo-controlled double-blind trial J. Neurosurg. 1992, 76 (4) 571-7
-
(1992)
J. Neurosurg.
, vol.76
, Issue.4
, pp. 571-577
-
-
Shibuya, M.1
Suzuki, Y.2
Sugita, K.3
Saito, I.4
Sasaki, T.5
Takakura, K.6
Nagata, I.7
Kikuchi, H.8
Takemae, T.9
Hidaka, H.10
-
61
-
-
84861600515
-
PRKX, TTBK2 and RSK4 expression causes Sunitinib resistance in kidney carcinoma- and melanoma-cell lines
-
Bender, C.; Ullrich, A. PRKX, TTBK2 and RSK4 expression causes Sunitinib resistance in kidney carcinoma- and melanoma-cell lines Int. J. Cancer 2012, 131 (2) E45-E55
-
(2012)
Int. J. Cancer
, vol.131
, Issue.2
, pp. E45-E55
-
-
Bender, C.1
Ullrich, A.2
-
62
-
-
79960555189
-
PRKX critically regulates endothelial cell proliferation, migration, and vascular-like structure formation
-
Li, X.; Iomini, C.; Hyink, D.; Wilson, P. D. PRKX critically regulates endothelial cell proliferation, migration, and vascular-like structure formation Dev. Biol. 2011, 356 (2) 475-85
-
(2011)
Dev. Biol.
, vol.356
, Issue.2
, pp. 475-485
-
-
Li, X.1
Iomini, C.2
Hyink, D.3
Wilson, P.D.4
-
63
-
-
33749538874
-
The Rho kinase inhibitor fasudil inhibits tumor progression in human and rat tumor models
-
Ying, H.; Biroc, S. L.; Li, W. W.; Alicke, B.; Xuan, J. A.; Pagila, R.; Ohashi, Y.; Okada, T.; Kamata, Y.; Dinter, H. The Rho kinase inhibitor fasudil inhibits tumor progression in human and rat tumor models Mol. Cancer Ther 2006, 5 (9) 2158-64
-
(2006)
Mol. Cancer Ther
, vol.5
, Issue.9
, pp. 2158-2164
-
-
Ying, H.1
Biroc, S.L.2
Li, W.W.3
Alicke, B.4
Xuan, J.A.5
Pagila, R.6
Ohashi, Y.7
Okada, T.8
Kamata, Y.9
Dinter, H.10
-
64
-
-
77954412580
-
Rho-kinase inhibitor, fasudil, suppresses glioblastoma cell line progression in vitro and in vivo
-
Deng, L.; Li, G.; Li, R.; Liu, Q.; He, Q.; Zhang, J. Rho-kinase inhibitor, fasudil, suppresses glioblastoma cell line progression in vitro and in vivo Cancer Biol. Ther 2010, 9 (11) 875-84
-
(2010)
Cancer Biol. Ther
, vol.9
, Issue.11
, pp. 875-884
-
-
Deng, L.1
Li, G.2
Li, R.3
Liu, Q.4
He, Q.5
Zhang, J.6
-
65
-
-
67049118923
-
Accurate and sensitive peptide identification with Mascot Percolator
-
Brosch, M.; Yu, L.; Hubbard, T.; Choudhary, J. Accurate and sensitive peptide identification with Mascot Percolator J. Proteome Res. 2009, 8 (6) 3176-81
-
(2009)
J. Proteome Res.
, vol.8
, Issue.6
, pp. 3176-3181
-
-
Brosch, M.1
Yu, L.2
Hubbard, T.3
Choudhary, J.4
-
66
-
-
77952283597
-
Toward a unified approach to dose-response modeling in ecotoxicology
-
Ritz, C. Toward a unified approach to dose-response modeling in ecotoxicology Environ. Toxicol. Chem. 2010, 29 (1) 220-9
-
(2010)
Environ. Toxicol. Chem.
, vol.29
, Issue.1
, pp. 220-229
-
-
Ritz, C.1
-
67
-
-
84901611036
-
Mass-spectrometry-based draft of the human proteome
-
Wilhelm, M.; Schlegl, J.; Hahne, H.; Moghaddas Gholami, A.; Lieberenz, M.; Savitski, M. M.; Ziegler, E.; Butzmann, L.; Gessulat, S.; Marx, H.; Mathieson, T.; Lemeer, S.; Schnatbaum, K.; Reimer, U.; Wenschuh, H.; Mollenhauer, M.; Slotta-Huspenina, J.; Boese, J. H.; Bantscheff, M.; Gerstmair, A.; Faerber, F.; Kuster, B. Mass-spectrometry-based draft of the human proteome Nature 2014, 509 (7502) 582-7
-
(2014)
Nature
, vol.509
, Issue.7502
, pp. 582-587
-
-
Wilhelm, M.1
Schlegl, J.2
Hahne, H.3
Moghaddas Gholami, A.4
Lieberenz, M.5
Savitski, M.M.6
Ziegler, E.7
Butzmann, L.8
Gessulat, S.9
Marx, H.10
Mathieson, T.11
Lemeer, S.12
Schnatbaum, K.13
Reimer, U.14
Wenschuh, H.15
Mollenhauer, M.16
Slotta-Huspenina, J.17
Boese, J.H.18
Bantscheff, M.19
Gerstmair, A.20
Faerber, F.21
Kuster, B.22
more..
|