-
1
-
-
0029849620
-
Cancer cell cycles
-
Sherr, C. J. Cancer cell cycles. Science 1996, 274, (5293)), 1672-1677.
-
(1996)
Science
, vol.274
, Issue.5293
, pp. 1672-1677
-
-
Sherr, C.J.1
-
2
-
-
0642378446
-
Cell cycle deregulation: A common motif in cancer
-
Meijer, L.; Jézéquel, A., Roberge, M., Eds.
-
Malumbers, M.; Carnero, A. Cell cycle deregulation: a common motif in cancer. In Progress in Cell Cycle Research; Meijer, L.; Jézéquel, A., Roberge, M., Eds.; 2003; Vol. 5, pp 5-18.
-
(2003)
Progress in Cell Cycle Research
, vol.5
, pp. 5-18
-
-
Malumbers, M.1
Carnero, A.2
-
3
-
-
0347917093
-
Cell-cycle targeted therapies
-
Swanton, C. Cell-cycle targeted therapies. Lancet Oncol. 2004, 5, (1), 27-36.
-
(2004)
Lancet Oncol.
, vol.5
, Issue.1
, pp. 27-36
-
-
Swanton, C.1
-
4
-
-
0031895560
-
Cyclin D1 and human neoplasia
-
Donnellan, R.; Chetty, R. Cyclin D1 and human neoplasia. Mol. Pathol. 1998, 51, (1)), 1-7.
-
(1998)
Mol. Pathol.
, vol.51
, Issue.1
, pp. 1-7
-
-
Donnellan, R.1
Chetty, R.2
-
5
-
-
0032517341
-
The p16INK4a/CDKN2A tumor suppressor and its relatives
-
Ruas, M.; Peters, G. The p16INK4a/CDKN2A tumor suppressor and its relatives. Biochim. Biophys. Acta 1998, 1378, (2)), F115-77.
-
(1998)
Biochim. Biophys. Acta
, vol.1378
, Issue.2
-
-
Ruas, M.1
Peters, G.2
-
6
-
-
0031466305
-
Cyclin-dependent kinases: Engines, clocks and microprocessors
-
Morgan, D. O. Cyclin-dependent kinases: Engines, Clocks and Microprocessors. Annu. Rev. Cell Dev. Biol. 1997, 13, 261-291.
-
(1997)
Annu. Rev. Cell Dev. Biol.
, vol.13
, pp. 261-291
-
-
Morgan, D.O.1
-
7
-
-
16944363001
-
Decreased levels of the cell-cycle inhibitor p27Kip1 protein: Prognostic implications in primary breast cancer
-
Catzavelos, C.; Bhattacharya, N.; Ung, Y. C.; Wilson, J. A.; Roncari, L.; Sandhu, C.; Shaw, P.; Yeger, H.; Morava-Protzner, I.; Kapusta, L.; Franssen, E.; Pritchard, K. I.; Slingerland, J. M. Decreased levels of the cell-cycle inhibitor p27Kip1 protein: prognostic implications in primary breast cancer. Nat. Med. 1997, 3 (2), 227-230.
-
(1997)
Nat. Med.
, vol.3
, Issue.2
, pp. 227-230
-
-
Catzavelos, C.1
Bhattacharya, N.2
Ung, Y.C.3
Wilson, J.A.4
Roncari, L.5
Sandhu, C.6
Shaw, P.7
Yeger, H.8
Morava-Protzner, I.9
Kapusta, L.10
Franssen, E.11
Pritchard, K.I.12
Slingerland, J.M.13
-
8
-
-
0031048716
-
Expression of cell-cycle regulators p27Kip1 and cyclin E, alone and in combination, correlate with survival in young breast cancer patients
-
Porter, P. L.; Malone, K. E.; Heagerty, P. J.; Alexander, G. M.; Gatti, L. A.; Firpo, E. J.; Daling, J. R.; Roberts, J. M. Expression of cell-cycle regulators p27Kip1 and cyclin E, alone and in combination, correlate with survival in young breast cancer patients. Nat. Med. 1997, 3, (2), 222-225.
-
(1997)
Nat. Med.
, vol.3
, Issue.2
, pp. 222-225
-
-
Porter, P.L.1
Malone, K.E.2
Heagerty, P.J.3
Alexander, G.M.4
Gatti, L.A.5
Firpo, E.J.6
Daling, J.R.7
Roberts, J.M.8
-
9
-
-
0037079027
-
Cyclin E and survival in patients with breast cancer
-
Keyomarsi, K.; Tucker, S. L.; Buchholz, T. A.; Callister, M.; Ding, Y.; Hortobagyi, G. N.; Bedrosian, I.; Knickerbocker, C.; Toyofuku, W.; Lowe, M.; Herliczek, T. W.; Bacus, S. S. Cyclin E and survival in patients with breast cancer N. Engl. J. Med. 2002, 347 (20), 1566-1575.
-
(2002)
N. Engl. J. Med.
, vol.347
, Issue.20
, pp. 1566-1575
-
-
Keyomarsi, K.1
Tucker, S.L.2
Buchholz, T.A.3
Callister, M.4
Ding, Y.5
Hortobagyi, G.N.6
Bedrosian, I.7
Knickerbocker, C.8
Toyofuku, W.9
Lowe, M.10
Herliczek, T.W.11
Bacus, S.S.12
-
10
-
-
0029024015
-
Role of the ubiquitin-proteasome pathway in regulating abundance of the cyclin-dependent kinase inhibitor p27
-
Pagano, M.; Tam, S. W.; Theodoras, A. M.; Beer-Romero, P.; Del Sal, G.; Chau, V.; Yew, P. R.; Draetta, G. F.; Rolfe, M. Role of the ubiquitin-proteasome pathway in regulating abundance of the cyclin-dependent kinase inhibitor p27. Science 1995, 269 (5224), 682-685.
-
(1995)
Science
, vol.269
, Issue.5224
, pp. 682-685
-
-
Pagano, M.1
Tam, S.W.2
Theodoras, A.M.3
Beer-Romero, P.4
Del Sal, G.5
Chau, V.6
Yew, P.R.7
Draetta, G.F.8
Rolfe, M.9
-
11
-
-
0036181669
-
Designing inhibitors of cyclin-dependent kinases
-
Hardcastle, I.-R.; Golding, B.-T.; Griffin, R.-J. Designing inhibitors of cyclin-dependent kinases. Annu. Rev. Pharmacol. Toxicol. 2002, 42, 325-348.
-
(2002)
Annu. Rev. Pharmacol. Toxicol.
, vol.42
, pp. 325-348
-
-
Hardcastle, I.-R.1
Golding, B.-T.2
Griffin, R.-J.3
-
12
-
-
0034736093
-
Pyrido[2,3-d]pyrimidin-7-one inhibitors of cyclin-dependent kinases
-
Barvian, M.; Boschelli, D. H.; Cossrow, J.; Dobrusin, E.; Fattaey, A.; Fritsch, A.; Fry, D.; Harvey, P.; Keller, P.; Garrett, M.; La, F.; Leopold, W.; McNamara, D.; Quin, M.; Trumpp-Kallmeyer, S.; Toogood, P.; Wu, Z.; Zhang, E. Pyrido[2,3-d]pyrimidin-7-one inhibitors of cyclin-dependent kinases. J. Med. Chem. 2000, 43 (24), 4606-4616.
-
(2000)
J. Med. Chem.
, vol.43
, Issue.24
, pp. 4606-4616
-
-
Barvian, M.1
Boschelli, D.H.2
Cossrow, J.3
Dobrusin, E.4
Fattaey, A.5
Fritsch, A.6
Fry, D.7
Harvey, P.8
Keller, P.9
Garrett, M.10
La, F.11
Leopold, W.12
McNamara, D.13
Quin, M.14
Trumpp-Kallmeyer, S.15
Toogood, P.16
Wu, Z.17
Zhang, E.18
-
13
-
-
0034618674
-
Inhibition of cyclin-dependent kinase 4 (Cdk4) by fascaplysin, a marine natural product
-
Soni, R.; Muller, L.; Furet, P.; Schoepfer, J.; Stephan, C.; Zumstein-Mecker, S.; Fretz, H.; Chaudhuri, B. Inhibition of cyclin-dependent kinase 4 (Cdk4) by fascaplysin, a marine natural product. Biochem. Biophys. Res. Commun. 2000, 275, (3)), 877-884.
-
(2000)
Biochem. Biophys. Res. Commun.
, vol.275
, Issue.3
, pp. 877-884
-
-
Soni, R.1
Muller, L.2
Furet, P.3
Schoepfer, J.4
Stephan, C.5
Zumstein-Mecker, S.6
Fretz, H.7
Chaudhuri, B.8
-
14
-
-
0035924235
-
Structure-based generation of a new class of potent Cdk4 inhibitors: New de novo design strategy and library design
-
Honma, T.; Hayashi, K.; Aoyama, T.; Hashimoto, N.; Machida, T.; Fukasawa, K.; Iwama, T.; Ikeura, C.; Ikuta, M.; Suzuki-Takahashi, I.; Iwasawa, Y.; Hayama, T.; Nishimura, S.; Morishima, H. Structure-based generation of a new class of potent Cdk4 inhibitors: new de novo design strategy and library design. J. Med. Chem. 2001, 44, (26)), 4615-4627.
-
(2001)
J. Med. Chem.
, vol.44
, Issue.26
, pp. 4615-4627
-
-
Honma, T.1
Hayashi, K.2
Aoyama, T.3
Hashimoto, N.4
Machida, T.5
Fukasawa, K.6
Iwama, T.7
Ikeura, C.8
Ikuta, M.9
Suzuki-Takahashi, I.10
Iwasawa, Y.11
Hayama, T.12
Nishimura, S.13
Morishima, H.14
-
15
-
-
0028103275
-
The CCP4 suite: Programs for protein crystallography
-
CCP4. The CCP4 suite: programs for protein crystallography. Acta Crystallogr. D 1994, 50, 760-763.
-
(1994)
Acta Crystallogr. D
, vol.50
, pp. 760-763
-
-
-
16
-
-
0027182223
-
Crystal structure of cyclin-dependent kinase 2
-
De Bondt, H. L.; Rosenblatt, J.; Jancarik, J.; Jones, H. D.; Morgan, D. O.; Kim, S.-H. Crystal structure of cyclin-dependent kinase 2. Nature 1993, 363, 595-602.
-
(1993)
Nature
, vol.363
, pp. 595-602
-
-
De Bondt, H.L.1
Rosenblatt, J.2
Jancarik, J.3
Jones, H.D.4
Morgan, D.O.5
Kim, S.-H.6
-
17
-
-
0029767016
-
Structural basis of cyclin-dependent kinase activation by phosphorylation
-
Russo, A. A.; Jeffrey, P. D.; Pavletich, N. P. Structural basis of cyclin-dependent kinase activation by phosphorylation. Nat. Struct. Biol. 1996, 3 (8), 696-700.
-
(1996)
Nat. Struct. Biol.
, vol.3
, Issue.8
, pp. 696-700
-
-
Russo, A.A.1
Jeffrey, P.D.2
Pavletich, N.P.3
-
18
-
-
0036785882
-
Structure-based design of a potent purine-based cyclin-dependent kinase inhibitor
-
Davies, T.-G.; Bentley, J.; Arris, C.-E.; Boyle, F. T.; Curtin, N.-J.; Endicott, J.-A.; Gibson, A.-E.; Golding, B.-T.; Griffin, R.-J.; Hardcastle, I.-R.; Jewsbury, P.; Johnson, L.-N.; Mesguiche, V.; Newell, D.-R.; Noble, M.-E. M.; Tucker, J.-A.; Wang, L.; Whitfield, H.-J. Structure-based design of a potent purine-based cyclin-dependent kinase inhibitor. Nat. Struct. Biol. 2002, 9 (10), 745-749.
-
(2002)
Nat. Struct. Biol.
, vol.9
, Issue.10
, pp. 745-749
-
-
Davies, T.-G.1
Bentley, J.2
Arris, C.-E.3
Boyle, F.T.4
Curtin, N.-J.5
Endicott, J.-A.6
Gibson, A.-E.7
Golding, B.-T.8
Griffin, R.-J.9
Hardcastle, I.-R.10
Jewsbury, P.11
Johnson, L.-N.12
Mesguiche, V.13
Newell, D.-R.14
Noble, M.-E.M.15
Tucker, J.-A.16
Wang, L.17
Whitfield, H.-J.18
-
19
-
-
0032563315
-
Exploiting chemical libraries, structure, and genomics in the search for kinase inhibitors
-
Gray, N. S.; Wodicka, L.; Thunnissen, A. M.; Norman, T. C.; Kwon, S.; Espinoza, F. H.; Morgan, D. O.; Barnes, G.; LeClerc, S.; Meijer, L.; Kim, S. H.; Lockhart, D. J.; Schultz, P. G. Exploiting chemical libraries, structure, and genomics in the search for kinase inhibitors. Science 1998, 281 (5376), 533-538.
-
(1998)
Science
, vol.281
, Issue.5376
, pp. 533-538
-
-
Gray, N.S.1
Wodicka, L.2
Thunnissen, A.M.3
Norman, T.C.4
Kwon, S.5
Espinoza, F.H.6
Morgan, D.O.7
Barnes, G.8
LeClerc, S.9
Meijer, L.10
Kim, S.H.11
Lockhart, D.J.12
Schultz, P.G.13
-
20
-
-
0034988970
-
Inhibitor binding to active and inactive CDK2: The crystal structure of CDK2-cyclin A/indirubin-5-sulphonate
-
Davies, T. G.; Tunnah, P.; Meijer, L.; Marko, D.; Eisenbrand, G.; Endicott, J. A.; Noble, M. E. Inhibitor binding to active and inactive CDK2: the crystal structure of CDK2-cyclin A/indirubin-5-sulphonate. Structure (Camb) 2001, 9 (5), 389-397.
-
(2001)
Structure (Camb)
, vol.9
, Issue.5
, pp. 389-397
-
-
Davies, T.G.1
Tunnah, P.2
Meijer, L.3
Marko, D.4
Eisenbrand, G.5
Endicott, J.A.6
Noble, M.E.7
-
21
-
-
0034010742
-
Inhibition of cyclin-dependent kinases, GSK-3beta and CK1 by hymenialdisine, a marine sponge constituent
-
Meijer, L.; Thunnissen, A. M.; White, A. W.; Garnier, M.; Nikolic, M.; Tsai, L. H.; Walter, J.; Cleverley, K. E.; Salinas, P. C.; Wu, Y. Z.; Biernat, J.; Mandelkow, E. M.; Kim, S. H.; Pettit, G. R. Inhibition of cyclin-dependent kinases, GSK-3beta and CK1 by hymenialdisine, a marine sponge constituent. Chem. Biol. 2000, 7 (1), 51-63.
-
(2000)
Chem. Biol.
, vol.7
, Issue.1
, pp. 51-63
-
-
Meijer, L.1
Thunnissen, A.M.2
White, A.W.3
Garnier, M.4
Nikolic, M.5
Tsai, L.H.6
Walter, J.7
Cleverley, K.E.8
Salinas, P.C.9
Wu, Y.Z.10
Biernat, J.11
Mandelkow, E.M.12
Kim, S.H.13
Pettit, G.R.14
-
22
-
-
0035808599
-
Prevention of chemotherapy-induced alopecia in rats by CDK inhibitors
-
Davis, S. T.; Benson, B. G.; Bramson, H. N.; Chapman, D. E.; Dickerson, S. H.; Dold, K. M.; Eberwein, D. J.; Edelstein, M.; Frye, S. V.; Gampe, R. T., Jr.; Griffin, R. J.; Harris, P. A.; Hassell, A. M.; Holmes, W. D.; Hunter, R. N.; Knick, V. B.; Lackey, K.; Lovejoy, B.; Luzzio, M. J.; Murray, D.; Parker, P.; Rocque, W. J.; Shewchuk, L.; Veal, J. M.; Walker, D. H.; Kuyper, L. F. Prevention of chemotherapy-induced alopecia in rats by CDK inhibitors. Science 2001, 291 (5501), 134-137.
-
(2001)
Science
, vol.291
, Issue.5501
, pp. 134-137
-
-
Davis, S.T.1
Benson, B.G.2
Bramson, H.N.3
Chapman, D.E.4
Dickerson, S.H.5
Dold, K.M.6
Eberwein, D.J.7
Edelstein, M.8
Frye, S.V.9
Gampe Jr., R.T.10
Griffin, R.J.11
Harris, P.A.12
Hassell, A.M.13
Holmes, W.D.14
Hunter, R.N.15
Knick, V.B.16
Lackey, K.17
Lovejoy, B.18
Luzzio, M.J.19
Murray, D.20
Parker, P.21
Rocque, W.J.22
Shewchuk, L.23
Veal, J.M.24
Walker, D.H.25
Kuyper, L.F.26
more..
-
23
-
-
0034642482
-
Binding mode of the 4-anilinoquinazoline class of protein kinase inhibitor: X-ray crystallographic studies of 4-anilinoquinazolines bound to cyclin-dependent kinase 2 and p38 kinase
-
Shewchuk, L.; Hassell, A.; Wisely, B.; Rocque, W.; Holmes, W.; Veal, J.; Kuyper, L. F. Binding mode of the 4-anilinoquinazoline class of protein kinase inhibitor: X-ray crystallographic studies of 4-anilinoquinazolines bound to cyclin-dependent kinase 2 and p38 kinase. J. Med. Chem. 2000, 43 (1), 133-138.
-
(2000)
J. Med. Chem.
, vol.43
, Issue.1
, pp. 133-138
-
-
Shewchuk, L.1
Hassell, A.2
Wisely, B.3
Rocque, W.4
Holmes, W.5
Veal, J.6
Kuyper, L.F.7
-
24
-
-
0031253655
-
Protein kinase inhibition by staurosporine: Details of the molecular interaction determined by X-ray crystallographic analysis of a CDK2-staurosporine complex
-
Lawrie, A. M.; Noble, M. E. M.; Tunnah, P. R.; Brown, N. R.; Johnson, L. N.; Endicott, J. A. Protein kinase inhibition by staurosporine: details of the molecular interaction determined by X-ray crystallographic analysis of a CDK2-staurosporine complex. Nat. Struct. Biol. 1997, 4, 796-801.
-
(1997)
Nat. Struct. Biol.
, vol.4
, pp. 796-801
-
-
Lawrie, A.M.1
Noble, M.E.M.2
Tunnah, P.R.3
Brown, N.R.4
Johnson, L.N.5
Endicott, J.A.6
-
25
-
-
0031829372
-
Removing near-neighbour redundancy from large protein sequence collections
-
Holm, L.; Sander, C. Removing near-neighbour redundancy from large protein sequence collections. Bioinformatics 1998, 14 (5), 423-429.
-
(1998)
Bioinformatics
, vol.14
, Issue.5
, pp. 423-429
-
-
Holm, L.1
Sander, C.2
-
26
-
-
0025183708
-
Basic local alignment search tool
-
Altschul, S. F.; Gish, W.; Miller, W.; Myers, E. W.; Lipman, D. J. Basic local alignment search tool. J. Mol. Biol. 1990, 215, (3), 403-410.
-
(1990)
J. Mol. Biol.
, vol.215
, Issue.3
, pp. 403-410
-
-
Altschul, S.F.1
Gish, W.2
Miller, W.3
Myers, E.W.4
Lipman, D.J.5
-
27
-
-
0027968068
-
CLUSTAL W: Improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice
-
Thompson, J. D.; Higgins, D. G.; Gibson, T. J. CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. Nucleic Acids Res. 1994, 22 (22), 4673-4680.
-
(1994)
Nucleic Acids Res.
, vol.22
, Issue.22
, pp. 4673-4680
-
-
Thompson, J.D.1
Higgins, D.G.2
Gibson, T.J.3
-
28
-
-
0343471377
-
Modification of a PCR based site-directed mutagenesis method
-
Fisher, C. L.; Pei, G. K. Modification of a PCR Based Site-Directed Mutagenesis Method. BioTechniques 1997, 23, 570-574.
-
(1997)
BioTechniques
, vol.23
, pp. 570-574
-
-
Fisher, C.L.1
Pei, G.K.2
-
29
-
-
0033224309
-
The structural basis for specificity of substrate and recruitment peptides for cyclin-dependent kinases
-
Brown, N. R.; Noble, M. E. M.; Endicott, J. E.; Johnson, L. N. The structural basis for specificity of substrate and recruitment peptides for cyclin-dependent kinases. Nat. Cell Biol. 1999, 1 (7), 438-443.
-
(1999)
Nat. Cell Biol.
, vol.1
, Issue.7
, pp. 438-443
-
-
Brown, N.R.1
Noble, M.E.M.2
Endicott, J.E.3
Johnson, L.N.4
-
30
-
-
0028093182
-
Inhibition of cyclin-dependent kinases by purine analogues
-
Vesely, J.; Havlicek, L.; Strnad, M.; Blow, J. J.; Donella-Deana, A.; Pinna, L.; Letham, D. S.; Kato, J.-Y.; Detivaud, L.; Leclerc, S.; Meijer, L. Inhibition of cyclin-dependent kinases by purine analogues. Eur. J. Biochem. 1994, 224, 771-786.
-
(1994)
Eur. J. Biochem.
, vol.224
, pp. 771-786
-
-
Vesely, J.1
Havlicek, L.2
Strnad, M.3
Blow, J.J.4
Donella-Deana, A.5
Pinna, L.6
Letham, D.S.7
Kato, J.-Y.8
Detivaud, L.9
Leclerc, S.10
Meijer, L.11
-
31
-
-
0003076963
-
Recent changes to the MOSFLM package for processing film and image plate data joint CCP4 and ESF-EAMCB
-
Leslie, A. G. W. Recent changes to the MOSFLM package for processing film and image plate data Joint CCP4 and ESF-EAMCB. Newsl. Protein Crystallogr. 1992, 26.
-
(1992)
Newsl. Protein Crystallogr.
, pp. 26
-
-
Leslie, A.G.W.1
-
32
-
-
0002454081
-
-
Science and Engineering Research Council UK: Daresbury Laboratory, Warrington
-
Evans, P. R. Data Reduction; Science and Engineering Research Council UK: Daresbury Laboratory, Warrington, 1993; pp 114-122.
-
(1993)
Data Reduction
, pp. 114-122
-
-
Evans, P.R.1
-
33
-
-
0030924992
-
Refinement of macromolecular structures by the maximum-liklihood method
-
Murshudov, G. N.; Vagin, A. A.; Dodson, E. J. Refinement of macromolecular structures by the maximum-liklihood method. Acta Crystallogr. D 1997, 53, 240-255.
-
(1997)
Acta Crystallogr. D
, vol.53
, pp. 240-255
-
-
Murshudov, G.N.1
Vagin, A.A.2
Dodson, E.J.3
-
34
-
-
84889120137
-
Improved methods for binding protein models in electron density maps and the location of errors in these models
-
Jones, T. A.; Zou, J. Y.; Cowan, S. W.; Kjeldgaard. Improved methods for binding protein models in electron density maps and the location of errors in these models. Acta Crystallogr A 1991, 47 (2), 110-119.
-
(1991)
Acta Crystallogr. A
, vol.47
, Issue.2
, pp. 110-119
-
-
Jones, T.A.1
Zou, J.Y.2
Cowan, S.W.3
Kjeldgaard4
-
35
-
-
0032964481
-
Automated protein model building combined with iterative structure refinement
-
Perrakis, A.; Morris, R.; Lamzin, V. S. Automated protein model building combined with iterative structure refinement. Nat. Struct. Biol. 1999, 6 (5), 458-463.
-
(1999)
Nat. Struct. Biol.
, vol.6
, Issue.5
, pp. 458-463
-
-
Perrakis, A.1
Morris, R.2
Lamzin, V.S.3
-
36
-
-
12444262227
-
Cyclin-dependent kinase 4 inhibitors as a treatment for cancer. Part 1: Identification and optimisation of substituted 4,6-Bis anilino pyrimidines
-
Beattie, J. F.; Breault, G. A.; Ellston, R. P.; Green, S.; Jewsbury, P. J.; Midgley, C. J.; Naven, R. T.; Minshull, C. A.; Pauptit, R. A.; Tucker, J. A.; Pease, J. E. Cyclin-dependent kinase 4 inhibitors as a treatment for cancer. Part 1: identification and optimisation of substituted 4,6-Bis anilino pyrimidines. Bioorg. Med. Chem. Lett. 2003, 13 (18), 2955-2960.
-
(2003)
Bioorg. Med. Chem. Lett.
, vol.13
, Issue.18
, pp. 2955-2960
-
-
Beattie, J.F.1
Breault, G.A.2
Ellston, R.P.3
Green, S.4
Jewsbury, P.J.5
Midgley, C.J.6
Naven, R.T.7
Minshull, C.A.8
Pauptit, R.A.9
Tucker, J.A.10
Pease, J.E.11
-
37
-
-
12444273643
-
Cyclin-dependent kinase 4 inhibitors as a treatment for cancer. Part 2: Identification and optimisation of substituted 2,4-bis anilino pyrimidines
-
Breault, G. A.; Ellston, R. P.; Green, S.; James, S. R.; Jewsbury, P. J.; Midgley, C. J.; Pauptit, R. A.; Minshull, C. A.; Tucker, J. A.; Pease, J. E. Cyclin-dependent kinase 4 inhibitors as a treatment for cancer. Part 2: identification and optimisation of substituted 2,4-bis anilino pyrimidines. Bioorg. Med. Chem. Lett. 2003, 13 (18), 2961-2966.
-
(2003)
Bioorg. Med. Chem. Lett.
, vol.13
, Issue.18
, pp. 2961-2966
-
-
Breault, G.A.1
Ellston, R.P.2
Green, S.3
James, S.R.4
Jewsbury, P.J.5
Midgley, C.J.6
Pauptit, R.A.7
Minshull, C.A.8
Tucker, J.A.9
Pease, J.E.10
-
38
-
-
0035924240
-
A novel approach for the development of selective Cdk4 inhibitors: Library design based on locations of Cdk4 specific amino acid residues
-
Honma, T.; Yoshizumi, T.; Hashimoto, N.; Hayashi, K.; Kawanishi, N.; Fukasawa, K.; Takaki, T.; Ikeura, C.; Ikuta, M.; Suzuki-Takahashi, I.; Hayama, T.; Nishimura, S.; Morishima, H. A novel approach for the development of selective Cdk4 inhibitors: library design based on locations of Cdk4 specific amino acid residues. J. Med. Chem. 2001, 44 (26), 4628-4640.
-
(2001)
J. Med. Chem.
, vol.44
, Issue.26
, pp. 4628-4640
-
-
Honma, T.1
Yoshizumi, T.2
Hashimoto, N.3
Hayashi, K.4
Kawanishi, N.5
Fukasawa, K.6
Takaki, T.7
Ikeura, C.8
Ikuta, M.9
Suzuki-Takahashi, I.10
Hayama, T.11
Nishimura, S.12
Morishima, H.13
-
39
-
-
0035920248
-
Crystallographic approach to identification of cyclin-dependent kinase 4 (CDK4)-specific inhibitors by using CDK4 mimic CDK2 protein
-
Ikuta, M.; Kamata, K.; Fukasawa, K.; Honma, T.; Machida, T.; Hirai, H.; Suzuki-Takahashi, I.; Hayama, T.; Nishimura, S. Crystallographic approach to identification of cyclin-dependent kinase 4 (CDK4)-specific inhibitors by using CDK4 mimic CDK2 protein. J. Biol. Chem. 2001, 276 (29), 27548-2754.
-
(2001)
J. Biol. Chem.
, vol.276
, Issue.29
, pp. 27548-32754
-
-
Ikuta, M.1
Kamata, K.2
Fukasawa, K.3
Honma, T.4
Machida, T.5
Hirai, H.6
Suzuki-Takahashi, I.7
Hayama, T.8
Nishimura, S.9
-
40
-
-
3142580855
-
N2-substituted O6-cyclohexylmethylguanine derivatives: Potent inhibitors of cyclin-dependent kinases 1 and 2
-
Hardcastle, I. R.; Arris, C. E.; Bentley, J.; Boyle, F. T.; Chen, Y.; Curtin, N. J.; Endicott, J. A.; Gibson, A. E.; Golding, B. T.; Griffin, R. J.; Jewsbury, P.; Menyerol, J.; Mesguiche, V.; Newell, D. R.; Noble, M. E.; Pratt, D. J.; Wang, L. Z.; Whitfield, H. J. N2-substituted O6-cyclohexylmethylguanine derivatives: potent inhibitors of cyclin-dependent kinases 1 and 2. J. Med. Chem. 2004, 47 (15), 3710-3722.
-
(2004)
J. Med. Chem.
, vol.47
, Issue.15
, pp. 3710-3722
-
-
Hardcastle, I.R.1
Arris, C.E.2
Bentley, J.3
Boyle, F.T.4
Chen, Y.5
Curtin, N.J.6
Endicott, J.A.7
Gibson, A.E.8
Golding, B.T.9
Griffin, R.J.10
Jewsbury, P.11
Menyerol, J.12
Mesguiche, V.13
Newell, D.R.14
Noble, M.E.15
Pratt, D.J.16
Wang, L.Z.17
Whitfield, H.J.18
-
41
-
-
19744365702
-
A small molecule-kinase interaction map for clinical kinase inhibitors
-
Fabian, M. A.; Biggs, W. H., 3rd; Treiber, D. K.; Atteridge, C. E.; Azimioara, M. D.; Benedetti, M. G.; Carter, T. A.; Ciceri, P.; Edeen, P. T.; Floyd, M.; Ford, J. M.; Galvin, M.; Gerlach, J. L.; Grotzfeld, R. M.; Herrgard, S.; Insko, D. E.; Insko, M. A.; Lai, A. G.; Lelias, J. M.; Mehta, S. A.; Milanov, Z. V.; Velasco, A. M.; Wodicka, L. M.; Patel, H. K.; Zarrinkar, P. P.; Lockhart, D. J. A small molecule-kinase interaction map for clinical kinase inhibitors. Nat. Biotechnol. 2005, 23 (3), 329-336.
-
(2005)
Nat. Biotechnol.
, vol.23
, Issue.3
, pp. 329-336
-
-
Fabian, M.A.1
Biggs III, W.H.2
Treiber, D.K.3
Atteridge, C.E.4
Azimioara, M.D.5
Benedetti, M.G.6
Carter, T.A.7
Ciceri, P.8
Edeen, P.T.9
Floyd, M.10
Ford, J.M.11
Galvin, M.12
Gerlach, J.L.13
Grotzfeld, R.M.14
Herrgard, S.15
Insko, D.E.16
Insko, M.A.17
Lai, A.G.18
Lelias, J.M.19
Mehta, S.A.20
Milanov, Z.V.21
Velasco, A.M.22
Wodicka, L.M.23
Patel, H.K.24
Zarrinkar, P.P.25
Lockhart, D.J.26
more..
-
42
-
-
16644397843
-
Developments in the CCP4 molecular-graphics project
-
Potterton, L.; McNicholas, S.; Krissinel, E.; Gruber, J.; Cowtan, K.; Emsley, P.; Murshudov, G. N.; Cohen, S.; Perrakis, A.; Noble, M. Developments in the CCP4 molecular-graphics project. Acta Crystallogr. D Biol. Crystallogr. 2004, 60 (Pt 12, Pt 1), 2288-2294.
-
(2004)
Acta Crystallogr. D Biol. Crystallogr.
, vol.60
, Issue.PART 12 AND PART 1
, pp. 2288-2294
-
-
Potterton, L.1
McNicholas, S.2
Krissinel, E.3
Gruber, J.4
Cowtan, K.5
Emsley, P.6
Murshudov, G.N.7
Cohen, S.8
Perrakis, A.9
Noble, M.10
-
43
-
-
0000243829
-
PROCHECK: A program to check the stereochemical quality of protein structures
-
Laskowski, R. A.; MacArthur, M. W.; Moss, D. S.; Thornton, J. M. PROCHECK: a program to check the stereochemical quality of protein structures. J. Appl. Crystallogr. 1993, 26, 283-291.
-
(1993)
J. Appl. Crystallogr.
, vol.26
, pp. 283-291
-
-
Laskowski, R.A.1
MacArthur, M.W.2
Moss, D.S.3
Thornton, J.M.4
|