1
|
The structure of P-TEFb (CDK9/cyclin T1), its complex with flavopiridol and regulation by phosphorylation.
|
EMBO J
|
2008
|
2.36
|
2
|
Identification of Mcm2 phosphorylation sites by S-phase-regulating kinases.
|
J Biol Chem
|
2006
|
2.04
|
3
|
Structural basis for CARM1 inhibition by indole and pyrazole inhibitors.
|
Biochem J
|
2011
|
1.20
|
4
|
Identification of Myb-binding protein 1A (MYBBP1A) as a novel substrate for aurora B kinase.
|
J Biol Chem
|
2010
|
0.89
|
5
|
Monolithic capillary columns for liquid chromatography-electrospray ionization mass spectrometry in proteomic and genomic research.
|
J Chromatogr B Analyt Technol Biomed Life Sci
|
2002
|
0.89
|
6
|
A Perl procedure for protein identification by Peptide Mass Fingerprinting.
|
BMC Bioinformatics
|
2009
|
0.83
|
7
|
Phosphorylation of TCTP as a marker for polo-like kinase-1 activity in vivo.
|
Anticancer Res
|
2010
|
0.80
|
8
|
Multidimensional proteomic analysis of photosynthetic membrane proteins by liquid extraction-ultracentrifugation-liquid chromatography-mass spectrometry.
|
Proteomics
|
2004
|
0.80
|
9
|
Synthesis and biological evaluation of RGD peptidomimetic-paclitaxel conjugates bearing lysosomally cleavable linkers.
|
Chemistry
|
2015
|
0.79
|
10
|
Discovery of 2-(cyclohexylmethylamino)pyrimidines as a new class of reversible valosine containing protein inhibitors.
|
J Med Chem
|
2014
|
0.79
|