| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A potent and selective inhibitor for the UBLCP1 proteasome phosphatase
|
He, Yantao
|
|
2015
|
23 |
12 |
p. 2798-2809
12 p.
|
artikel
|
| 2 |
A single-cell model of PIP3 dynamics using chemical dimerization
|
MacNamara, Aidan
|
|
2015
|
23 |
12 |
p. 2868-2876
9 p.
|
artikel
|
| 3 |
Azide–alkyne cycloaddition-mediated cyclization of phosphonopeptides and their evaluation as PTP1B binders and enrichment tools
|
Meyer, Christoph
|
|
2015
|
23 |
12 |
p. 2848-2853
6 p.
|
artikel
|
| 4 |
Biology-oriented synthesis of benzopyrano[3,4-c]pyrrolidines
|
Potowski, Marco
|
|
2015
|
23 |
12 |
p. 2895-2903
9 p.
|
artikel
|
| 5 |
Chemistry and biology of protein and inositol phosphorylation
|
Köhn, Maja
|
|
2015
|
23 |
12 |
p. 2747-2748
2 p.
|
artikel
|
| 6 |
Design of a selenylsulfide-bridged EGFR dimerization arm mimic
|
Hanold, Laura E.
|
|
2015
|
23 |
12 |
p. 2761-2766
6 p.
|
artikel
|
| 7 |
Desymmetrization of myo-inositol derivatives by lanthanide catalyzed phosphitylation with C 2-symmetric phosphites
|
Duss, Michael
|
|
2015
|
23 |
12 |
p. 2854-2861
8 p.
|
artikel
|
| 8 |
Developing new chemical tools for DNA methyltransferase 1 (DNMT 1): A small-molecule activity-based probe and novel tetrazole-containing inhibitors
|
Zhu, Biwei
|
|
2015
|
23 |
12 |
p. 2917-2927
11 p.
|
artikel
|
| 9 |
Editorial board
|
|
|
2015
|
23 |
12 |
p. IFC-
1 p.
|
artikel
|
| 10 |
Graphical contents list
|
|
|
2015
|
23 |
12 |
p. 2741-2746
6 p.
|
artikel
|
| 11 |
Light-switched inhibitors of protein tyrosine phosphatase PTP1B based on phosphonocarbonyl phenylalanine as photoactive phosphotyrosine mimetic
|
Wagner, Stefan
|
|
2015
|
23 |
12 |
p. 2839-2847
9 p.
|
artikel
|
| 12 |
Molecular mechanisms of protein kinase regulation by calcium/calmodulin
|
Simon, Bertrand
|
|
2015
|
23 |
12 |
p. 2749-2760
12 p.
|
artikel
|
| 13 |
Native chemical ligation between asparagine and valine: Application and limitations for the synthesis of tri-phosphorylated C-terminal tau
|
Reimann, Oliver
|
|
2015
|
23 |
12 |
p. 2890-2894
5 p.
|
artikel
|
| 14 |
Perspective: Tyrosine phosphatases as novel targets for antiplatelet therapy
|
Tautz, Lutz
|
|
2015
|
23 |
12 |
p. 2786-2797
12 p.
|
artikel
|
| 15 |
Rational design of allosteric-inhibition sites in classical protein tyrosine phosphatases
|
Chio, Cynthia M.
|
|
2015
|
23 |
12 |
p. 2828-2838
11 p.
|
artikel
|
| 16 |
Reversible chemical dimerizer-induced recovery of PIP2 levels moves clathrin to the plasma membrane
|
Schifferer, Martina
|
|
2015
|
23 |
12 |
p. 2862-2867
6 p.
|
artikel
|
| 17 |
Semisynthesis and initial characterization of sortase A mutants containing selenocysteine and homocysteine
|
Schmohl, Lena
|
|
2015
|
23 |
12 |
p. 2883-2889
7 p.
|
artikel
|
| 18 |
Strategies to make protein serine/threonine (PP1, calcineurin) and tyrosine phosphatases (PTP1B) druggable: Achieving specificity by targeting substrate and regulatory protein interaction sites
|
Peti, Wolfgang
|
|
2015
|
23 |
12 |
p. 2781-2785
5 p.
|
artikel
|
| 19 |
Structure–activity studies in the development of a hydrazone based inhibitor of adipose-triglyceride lipase (ATGL)
|
Mayer, Nicole
|
|
2015
|
23 |
12 |
p. 2904-2916
13 p.
|
artikel
|
| 20 |
Structure-based design and synthesis of covalent-reversible inhibitors to overcome drug resistance in EGFR
|
Basu, Debjit
|
|
2015
|
23 |
12 |
p. 2767-2780
14 p.
|
artikel
|
| 21 |
Synthesis and biological evaluation of 3-aminoisoquinolin-1(2H)-one based inhibitors of the dual-specificity phosphatase Cdc25B
|
George Rosenker, Kara M.
|
|
2015
|
23 |
12 |
p. 2810-2818
9 p.
|
artikel
|
| 22 |
Synthesis of hydrolysis-resistant pyridoxal 5′-phosphate analogs and their biochemical and X-ray crystallographic characterization with the pyridoxal phosphatase chronophin
|
Knobloch, Gunnar
|
|
2015
|
23 |
12 |
p. 2819-2827
9 p.
|
artikel
|
| 23 |
Towards the computational design of protein post-translational regulation
|
Strumillo, Marta
|
|
2015
|
23 |
12 |
p. 2877-2882
6 p.
|
artikel
|
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