nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Accounting for global protein deformability during protein–protein and protein–ligand docking
|
May, Andreas |
|
2005 |
1754 |
1-2 |
p. 225-231 7 p. |
artikel |
2 |
Advances in the structural biology, design and clinical development of Bcr-Abl kinase inhibitors for the treatment of chronic myeloid leukaemia
|
Manley, Paul William |
|
2005 |
1754 |
1-2 |
p. 3-13 11 p. |
artikel |
3 |
Alternative splicing: A new drug target of the post-genome era
|
Hagiwara, Masatoshi |
|
2005 |
1754 |
1-2 |
p. 324-331 8 p. |
artikel |
4 |
Baker's yeast as a tool for the development of antifungal kinase inhibitors—targeting protein kinase C and the cell integrity pathway
|
Heinisch, Jürgen J. |
|
2005 |
1754 |
1-2 |
p. 171-182 12 p. |
artikel |
5 |
Characterisation of kinase-selective inhibitors by chemical proteomics
|
Daub, Henrik |
|
2005 |
1754 |
1-2 |
p. 183-190 8 p. |
artikel |
6 |
Coupling phosphoryl transfer and substrate interactions in protein kinases
|
Lieser, Scot A. |
|
2005 |
1754 |
1-2 |
p. 191-199 9 p. |
artikel |
7 |
Crystallography for protein kinase drug design: PKA and SRC case studies
|
Breitenlechner, Christine B. |
|
2005 |
1754 |
1-2 |
p. 38-49 12 p. |
artikel |
8 |
Development of specific Rho-kinase inhibitors and their clinical application
|
Tamura, Masahiro |
|
2005 |
1754 |
1-2 |
p. 245-252 8 p. |
artikel |
9 |
Dynamical binding of proline-rich peptides to their recognition domains
|
Gu, Wei |
|
2005 |
1754 |
1-2 |
p. 232-238 7 p. |
artikel |
10 |
Dynamics of signaling by PKA
|
Taylor, Susan S. |
|
2005 |
1754 |
1-2 |
p. 25-37 13 p. |
artikel |
11 |
Editorial Board
|
|
|
2005 |
1754 |
1-2 |
p. ii- 1 p. |
artikel |
12 |
Endogenous and synthetic inhibitors of the Src-family protein tyrosine kinases
|
Chong, Yuh-Ping |
|
2005 |
1754 |
1-2 |
p. 210-220 11 p. |
artikel |
13 |
Exploiting structural principles to design cyclin-dependent kinase inhibitors
|
Noble, Martin |
|
2005 |
1754 |
1-2 |
p. 58-64 7 p. |
artikel |
14 |
Features and potentials of ATP-site directed CK2 inhibitors
|
Sarno, Stefania |
|
2005 |
1754 |
1-2 |
p. 263-270 8 p. |
artikel |
15 |
Functional studies of protein tyrosine phosphatases with chemical approaches
|
Zhang, Zhong-Yin |
|
2005 |
1754 |
1-2 |
p. 100-107 8 p. |
artikel |
16 |
Involvement of the small protein tyrosine phosphatases TC-PTP and PTP1B in signal transduction and diseases: From diabetes, obesity to cell cycle, and cancer
|
Dubé, Nadia |
|
2005 |
1754 |
1-2 |
p. 108-117 10 p. |
artikel |
17 |
Mammalian histidine kinases
|
Besant, Paul G. |
|
2005 |
1754 |
1-2 |
p. 281-290 10 p. |
artikel |
18 |
MAPK signalling pathways as molecular targets for anti-inflammatory therapy—from molecular mechanisms to therapeutic benefits
|
Kaminska, Bozena |
|
2005 |
1754 |
1-2 |
p. 253-262 10 p. |
artikel |
19 |
Multiple molecular recognition mechanisms. Cytochrome P450—A case study
|
Wade, Rebecca C. |
|
2005 |
1754 |
1-2 |
p. 239-244 6 p. |
artikel |
20 |
Peptide inhibitors of protein kinases—discovery, characterisation and use
|
Bogoyevitch, Marie A. |
|
2005 |
1754 |
1-2 |
p. 79-99 21 p. |
artikel |
21 |
Protein kinases as drug targets in trypanosomes and Leishmania
|
Naula, Christina |
|
2005 |
1754 |
1-2 |
p. 151-159 9 p. |
artikel |
22 |
Protein kinases as targets for antimalarial intervention: Kinomics, structure-based design, transmission-blockade, and targeting host cell enzymes
|
Doerig, Christian |
|
2005 |
1754 |
1-2 |
p. 132-150 19 p. |
artikel |
23 |
Protein kinase structure and function analysis with chemical tools
|
Shen, Kui |
|
2005 |
1754 |
1-2 |
p. 65-78 14 p. |
artikel |
24 |
Proteins and Proteomics Cumulative Contents
|
|
|
2005 |
1754 |
1-2 |
p. 332-333 2 p. |
artikel |
25 |
P-Ser-HPr—a link between carbon metabolism and the virulence of some pathogenic bacteria
|
Deutscher, Josef |
|
2005 |
1754 |
1-2 |
p. 118-125 8 p. |
artikel |
26 |
Quantifying ERK2–protein interactions by fluorescence anisotropy: PEA-15 inhibits ERK2 by blocking the binding of DEJL domains
|
Callaway, Kari |
|
2005 |
1754 |
1-2 |
p. 316-323 8 p. |
artikel |
27 |
Reversible phosphorylation of histidine residues in vertebrate proteins
|
Klumpp, Susanne |
|
2005 |
1754 |
1-2 |
p. 291-295 5 p. |
artikel |
28 |
Signaling protein inhibitors via the combinatorial modification of peptide scaffolds
|
Lawrence, David S. |
|
2005 |
1754 |
1-2 |
p. 50-57 8 p. |
artikel |
29 |
Special issue—Inhibitors of protein kinases
|
Shugar, David |
|
2005 |
1754 |
1-2 |
p. 1-2 2 p. |
artikel |
30 |
Substrate specificity of protein kinases and computational prediction of substrates
|
Kobe, Boštjan |
|
2005 |
1754 |
1-2 |
p. 200-209 10 p. |
artikel |
31 |
Target flexibility in molecular recognition
|
McCammon, J. Andrew |
|
2005 |
1754 |
1-2 |
p. 221-224 4 p. |
artikel |
32 |
Targeting malaria with specific CDK inhibitors
|
Geyer, Jeanne A. |
|
2005 |
1754 |
1-2 |
p. 160-170 11 p. |
artikel |
33 |
Targeting protein kinase C and “non-kinase” phorbol ester receptors: Emerging concepts and therapeutic implications
|
Kazanietz, Marcelo G. |
|
2005 |
1754 |
1-2 |
p. 296-304 9 p. |
artikel |
34 |
Tetrabromobenzotriazole (TBBt) and tetrabromobenzimidazole (TBBz) as selective inhibitors of protein kinase CK2: Evaluation of their effects on cells and different molecular forms of human CK2
|
Zien, Piotr |
|
2005 |
1754 |
1-2 |
p. 271-280 10 p. |
artikel |
35 |
The bacterial HPr kinase/phosphorylase: A new type of Ser/Thr kinase as antimicrobial target
|
Nessler, Sylvie |
|
2005 |
1754 |
1-2 |
p. 126-131 6 p. |
artikel |
36 |
The RIO kinases: An atypical protein kinase family required for ribosome biogenesis and cell cycle progression
|
LaRonde-LeBlanc, Nicole |
|
2005 |
1754 |
1-2 |
p. 14-24 11 p. |
artikel |
37 |
The role of SMG-1 in nonsense-mediated mRNA decay
|
Yamashita, Akio |
|
2005 |
1754 |
1-2 |
p. 305-315 11 p. |
artikel |