M. Rabiller

发表

Proteus in the World of Proteins: Conformational Changes in Protein Kinases

Daniel Rauh, D. Rauh, Matthäus Getlik, 2010, Archiv der Pharmazie.

Human TPST1 transmembrane domain triggers enzyme dimerisation and localisation to the Golgi compartment.

C. Wotzlaw, J. W. Mueller, P. Bayer, 2006, Journal of molecular biology.

A molecular handshake

P. Bayer, M. Rabiller, 2002 .

Displacement assay for the detection of stabilizers of inactive kinase conformations.

C. Grütter, D. Rauh, M. Rabiller, 2010, Journal of Medicinal Chemistry.

Specification of SUMO 1-and SUMO 2-interacting Motifs *

I. Dikic, P. Bayer, M. Rabiller, 2006 .

Specification of SUMO1- and SUMO2-interacting Motifs*

Ivan Dikic, Peter Bayer, I. Dikic, 2006, Journal of Biological Chemistry.

High-throughput screening to identify inhibitors which stabilize inactive kinase conformations in p38alpha.

Daniel Rauh, Christian Ottmann, C. Ottmann, 2009, Journal of the American Chemical Society.

Hybrid compound design to overcome the gatekeeper T338M mutation in cSrc.

C. Grütter, D. Rauh, M. Rabiller, 2009, Journal of medicinal chemistry.

Dissecting Phosphorylation Networks: The Use of Analogue‐Sensitive Kinases and More Specific Kinase Inhibitors as Tools

D. Rauh, M. Rabiller, J. Simard, 2011 .

Characterization of Irreversible Kinase Inhibitors by Directly Detecting Covalent Bond Formation: A Tool for Dissecting Kinase Drug Resistance

C. Grütter, M. Rabiller, H. Raaijmakers, 2010, Chembiochem : a European journal of chemical biology.

Synthesis and biological evaluation of 4-anilinoquinolines as potent inhibitors of epidermal growth factor receptor.

Roman K. Thomas, M. Sos, W. V. van Otterlo, 2010, Journal of medicinal chemistry.

Chemogenomic profiling provides insights into the limited activity of irreversible EGFR Inhibitors in tumor cells expressing the T790M EGFR resistance mutation.

Martin Peifer, Daniel Rauh, Lars Ruddigkeit, 2010, Cancer research.

Development of a fluorescent-tagged kinase assay system for the detection and characterization of allosteric kinase inhibitors.

Daniel Rauh, Jeffrey R. Simard, C. Grütter, 2009, Journal of the American Chemical Society.

A new screening assay for allosteric inhibitors of cSrc.

Daniel Rauh, C. Grütter, D. Rauh, 2009, Nature chemical biology.

Structural insights into how irreversible inhibitors can overcome drug resistance in EGFR.

C. Grütter, D. Rauh, A. Michalczyk, 2008, Bioorganic & medicinal chemistry.

Fluorophore Labeled Kinase Detects Ligands That Bind within the MAPK Insert of p38α Kinase

W. V. van Otterlo, C. Grütter, D. Rauh, 2012, PloS one.

Characterization of Irreversible Kinase Inhibitors by Directly Detecting Covalent Bond Formation: A Tool for Dissecting Kinase Drug Resistance

C. Grütter, M. Rabiller, H. Raaijmakers, 2010, Chembiochem : a European journal of chemical biology.

Interactions of SUMO proteins

M. Rabiller, 2007 .

A new screening assay for allosteric inhibitors of cSrc.

C. Grütter, D. Rauh, M. Rabiller, 2009, Nature chemical biology.

High-throughput screening to identify inhibitors which stabilize inactive kinase conformations in p38alpha.

C. Ottmann, Alexander Wolf, C. Grütter, 2009, Journal of the American Chemical Society.