1
|
Small-molecule inhibition of Wee1 kinase by MK-1775 selectively sensitizes p53-deficient tumor cells to DNA-damaging agents.
|
Mol Cancer Ther
|
2009
|
2.50
|
2
|
Preferences for phosphorylation sites in the retinoblastoma protein of D-type cyclin-dependent kinases, Cdk4 and Cdk6, in vitro.
|
J Biochem
|
2005
|
1.11
|
3
|
Structures of the PKC-iota kinase domain in its ATP-bound and apo forms reveal defined structures of residues 533-551 in the C-terminal tail and their roles in ATP binding.
|
Acta Crystallogr D Biol Crystallogr
|
2010
|
0.89
|
4
|
Cdk-mediated phosphorylation of pRB regulates HDAC binding in vitro.
|
Biochem Biophys Res Commun
|
2004
|
0.85
|
5
|
Potent anti-tumor activity of a macrocycle-quinoxalinone class pan-Cdk inhibitor in vitro and in vivo.
|
Invest New Drugs
|
2010
|
0.78
|
6
|
Multiplexed random peptide library and phospho-specific antibodies facilitate human polo-like kinase 1 inhibitor screen.
|
Assay Drug Dev Technol
|
2010
|
0.77
|
7
|
Biological characterization of 2-aminothiazole-derived Cdk4/6 selective inhibitor in vitro and in vivo.
|
Cell Cycle
|
2010
|
0.76
|
8
|
Tracheoesophageal fistula closed by chemoradiotherapy in lung cancer.
|
Case Rep Oncol
|
2011
|
0.75
|
9
|
[Two cases of pulmonary tuberculosis with an intra-familial transmission route].
|
Kekkaku
|
2012
|
0.75
|