-
1
-
-
0345256169
-
-
5th ed., Proteome, Inc., Beverly, USA
-
Hodges, P.E. (ed). Yeast Proteome Handbook (1998, 5th ed.), Proteome, Inc., Beverly, USA.
-
(1998)
Yeast Proteome Handbook
-
-
Hodges, P.E.1
-
2
-
-
0028093182
-
Inhibition of cyclin-dependent kinases by purine analogues
-
Vesely, J., et al., & Meijer, L. (1994). Inhibition of cyclin-dependent kinases by purine analogues. Eur. J. Biochem. 224, 771-786.
-
(1994)
Eur. J. Biochem.
, vol.224
, pp. 771-786
-
-
Vesely, J.1
Meijer, L.2
-
3
-
-
0031037714
-
Biochemical and cellular effects of roscovitine, a potent and selective inhibitor of the cyclin-dependent kinases cdc2, cdk2 and cdk5
-
Meijer, L. et al., & Moulinoux, J.-P. (1997). Biochemical and cellular effects of roscovitine, a potent and selective inhibitor of the cyclin-dependent kinases cdc2, cdk2 and cdk5. Eur. J. Biochem. 243, 527-536.
-
(1997)
Eur. J. Biochem.
, vol.243
, pp. 527-536
-
-
Meijer, L.1
Moulinoux, J.-P.2
-
4
-
-
0029090514
-
Multiple modes of ligand recognition - Crystal structure of cyclin dependent protein kinase 2 in complexes with ATP and two inhibitors, olomoucine and isopentenyladenine
-
Schulze-Gahmen, U. et al., & Kim, S.-H. (1995). Multiple modes of ligand recognition - Crystal structure of cyclin dependent protein kinase 2 in complexes with ATP and two inhibitors, olomoucine and isopentenyladenine. Proteins 22, 378-391.
-
(1995)
Proteins
, vol.22
, pp. 378-391
-
-
Schulze-Gahmen, U.1
Kim, S.-H.2
-
5
-
-
0029317904
-
Cyclin-dependent protein kinases - Key regulators of the eukaryotic cell cycle
-
Nigg, E.A. (1995). Cyclin-dependent protein kinases - Key regulators of the eukaryotic cell cycle. BioEssays 17, 471-480.
-
(1995)
BioEssays
, vol.17
, pp. 471-480
-
-
Nigg, E.A.1
-
6
-
-
0029740469
-
A structure-based library approach to kinase inhibitors
-
Norman, T.C., Gray, N.S., Koh, J.T. & Schultz, P.G. (1996). A structure-based library approach to kinase inhibitors. J. Am. Chem. Soc. 118, 7430-7431.
-
(1996)
J. Am. Chem. Soc.
, vol.118
, pp. 7430-7431
-
-
Norman, T.C.1
Gray, N.S.2
Koh, J.T.3
Schultz, P.G.4
-
7
-
-
0031575637
-
Combinatorial synthesis of 2,9-substituted purines
-
Gray, N.S., Kwon, S. & Schultz, P.G. (1997). Combinatorial synthesis of 2,9-substituted purines. Tetrahedron Lett. 38, 1161-1164.
-
(1997)
Tetrahedron Lett.
, vol.38
, pp. 1161-1164
-
-
Gray, N.S.1
Kwon, S.2
Schultz, P.G.3
-
8
-
-
0031013919
-
Facile preparation of 2,6-disubstituted purines using solid-phase chemistry
-
Nugiel, D.A., Cornelius, L.A.M. & Corbett, J.W. (1997). Facile preparation of 2,6-disubstituted purines using solid-phase chemistry. J. Org. Chem. 62, 201-203.
-
(1997)
J. Org. Chem.
, vol.62
, pp. 201-203
-
-
Nugiel, D.A.1
Cornelius, L.A.M.2
Corbett, J.W.3
-
9
-
-
0032492705
-
Synthesis of C2 alkynylated purines, a new family of potent inhibitors of cyclin-dependent kinases
-
Legraverend, M., Ludwig, O., Bisagni, E., Leclerc, S. & Meijer, L. (1998). Synthesis of C2 alkynylated purines, a new family of potent inhibitors of cyclin-dependent kinases. Bioorg. Med. Chem. Lett. 8, 793-798.
-
(1998)
Bioorg. Med. Chem. Lett.
, vol.8
, pp. 793-798
-
-
Legraverend, M.1
Ludwig, O.2
Bisagni, E.3
Leclerc, S.4
Meijer, L.5
-
10
-
-
0030869845
-
Synthesis and activity of 2,6,9-trisubsituted purines
-
Schow, S.R., et al., & Lum, R.T. (1997). Synthesis and activity of 2,6,9-trisubsituted purines. Bioorg. Med. Chem. Lett. 7, 2697-2702.
-
(1997)
Bioorg. Med. Chem. Lett.
, vol.7
, pp. 2697-2702
-
-
Schow, S.R.1
Lum, R.T.2
-
11
-
-
0032568333
-
Solution-phase synthesis of 2,6,9-trisubstituted purines
-
Fiorini, M.T. & Abell, C. (1998). Solution-phase synthesis of 2,6,9-trisubstituted purines. Tetrahedron Lett. 39, 1827-1830.
-
(1998)
Tetrahedron Lett.
, vol.39
, pp. 1827-1830
-
-
Fiorini, M.T.1
Abell, C.2
-
12
-
-
0029993339
-
Structural basis for specificity and potency of a flavonoid inhibitor of human CDK2, a cell cycle kinase
-
de Azevedo, Jr., W.F., Mueller-Diechmann, H.-J., Schulze-Gahmen, U., Worland, P.J., Sausville, E. & Kim, S.-H. (1996). Structural basis for specificity and potency of a flavonoid inhibitor of human CDK2, a cell cycle kinase. Proc. Natl Acad. Sci. USA 93, 2735-2740.
-
(1996)
Proc. Natl Acad. Sci. USA
, vol.93
, pp. 2735-2740
-
-
De Azevedo W.F., Jr.1
Mueller-Diechmann, H.-J.2
Schulze-Gahmen, U.3
Worland, P.J.4
Sausville, E.5
Kim, S.-H.6
-
13
-
-
0031253655
-
Protein kinase inhibition by staurosporine revealed in details of the molecular interaction with CDK2
-
Lawrie, A.M., Noble, M.E.M., Tunnah, P., Brown, N.R., Johnson, L.N. & Endicott, J.A. (1997). Protein kinase inhibition by staurosporine revealed in details of the molecular interaction with CDK2. Nat. Struct. Biol. 4, 796-801.
-
(1997)
Nat. Struct. Biol.
, vol.4
, pp. 796-801
-
-
Lawrie, A.M.1
Noble, M.E.M.2
Tunnah, P.3
Brown, N.R.4
Johnson, L.N.5
Endicott, J.A.6
-
14
-
-
0000284254
-
The alkylation of 2-amino-6-chloropurine with alcohols by Mitsunobu reaction for a synthesis of carbocyclic guanosine analogs
-
Toyota, A., Katagiri, N. & Kaneko, C. (1993). The alkylation of 2-amino-6-chloropurine with alcohols by Mitsunobu reaction for a synthesis of carbocyclic guanosine analogs. Heterocycle 36, 1625-1630.
-
(1993)
Heterocycle
, vol.36
, pp. 1625-1630
-
-
Toyota, A.1
Katagiri, N.2
Kaneko, C.3
-
16
-
-
0032563315
-
Exploiting chemical libraries, structure and genomics in the search for kinase inhibitors
-
Gray, N.S., et al., & Schultz, P.G. (1998). Exploiting chemical libraries, structure and genomics in the search for kinase inhibitors. Science 281, 533-538.
-
(1998)
Science
, vol.281
, pp. 533-538
-
-
Gray, N.S.1
Schultz, P.G.2
-
17
-
-
0024595042
-
Re-examination and further development of a precise and rapid dye method for measuring cell growth/cell kill
-
Hansen, M.B., Nielsen, S.E. & Berg, K.J. (1989). Re-examination and further development of a precise and rapid dye method for measuring cell growth/cell kill. Immunol. Methods 119, 203-210.
-
(1989)
Immunol. Methods
, vol.119
, pp. 203-210
-
-
Hansen, M.B.1
Nielsen, S.E.2
Berg, K.J.3
-
18
-
-
0030061451
-
CDK2 kinase is required for entry into mitosis as a positive regulator of cdc2-cyclin B kinase activity
-
Guadagno, T.M. & Newport, J.W. (1996). CDK2 kinase is required for entry into mitosis as a positive regulator of cdc2-cyclin B kinase activity. Cell 84, 73-82.
-
(1996)
Cell
, vol.84
, pp. 73-82
-
-
Guadagno, T.M.1
Newport, J.W.2
-
19
-
-
0032559829
-
The coordination of centrosome reproduction with nuclear events of the cell cycle in the sea urchin zygote
-
Hinchliffe, E.H., Cassels, G.O., Rieder, C.L & Sluder, G. (1998). The coordination of centrosome reproduction with nuclear events of the cell cycle in the sea urchin zygote. J. Cell Biol. 140, 1417-1426.
-
(1998)
J. Cell Biol.
, vol.140
, pp. 1417-1426
-
-
Hinchliffe, E.H.1
Cassels, G.O.2
Rieder, C.L.3
Sluder, G.4
-
20
-
-
0031563780
-
The effect of the cyclin-dependent kinase inhibitor olomoucine on cell cycle kinetics
-
Schutte, B., Nieland, L., van Engeland, M., Henfling, M.E.R., Meijer, L. & Ramaekers, F.C.S. (1997). The effect of the cyclin-dependent kinase inhibitor olomoucine on cell cycle kinetics. Exp. Cell Res. 236, 4-15.
-
(1997)
Exp. Cell Res.
, vol.236
, pp. 4-15
-
-
Schutte, B.1
Nieland, L.2
Van Engeland, M.3
Henfling, M.E.R.4
Meijer, L.5
Ramaekers, F.C.S.6
-
21
-
-
0031194040
-
Roscovitine, a novel cyclin-dependent kinase inhibitor, characterizes restriction point and G2/M transition in tobacco BY-2 cell suspension
-
Planchais, S. et al., & Bergounioux, C. (1997). Roscovitine, a novel cyclin-dependent kinase inhibitor, characterizes restriction point and G2/M transition in tobacco BY-2 cell suspension. Plant J. 12, 191-202.
-
(1997)
Plant J.
, vol.12
, pp. 191-202
-
-
Planchais, S.1
Bergounioux, C.2
|