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Biological Chemistry
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November 20, 2002
Trypsin mutants for structure-based drug design: expression, refolding and crystallisation
Daniel Rauh, Sabine Reyda, Gerhard Klebe, et al.
The Journal of Biological Chemistry
|
October 2, 2008
Human carbonyl reductase 1 is an S-nitrosoglutathione reductase
Raynard L Bateman, Daniel Rauh, Brandon Tavshanjian, et al.
RSC Medicinal Chemistry
|
January 22, 2021
KRasG12C inhibitors in clinical trials: a short historical perspective
Lisa Goebel, Matthias P Müller, Roger S Goody, et al.
Current Opinion in Chemical Biology
|
May 5, 2009
The therapeutic potential of phosphatase inhibitors
Viktor V Vintonyak, Andrey P Antonchick, Daniel Rauh, et al.
Chemical Communications (Cambridge, England)
|
August 5, 2020
Conformational selection vs. induced fit: insights into the binding mechanisms of p38α MAP Kinase inhibitors
Patrick Roser, Jörn Weisner, Juliane Stehle, et al.
Angewandte Chemie (International Ed. in English)
|
August 24, 2017
Covalent Lipid Pocket Ligands Targeting p38α MAPK Mutants
Mike Bührmann, Julia Hardick, Jörn Weisner, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)
|
February 16, 2023
Insights into the Conformational Plasticity of the Protein Kinase Akt1 by Multi-Lateral Dipolar Spectroscopy
Juliane Stehle, Jörn Weisner, Leanne Eichhorn, et al.
Journal of the American Chemical Society
|
April 25, 2013
Selective detection of allosteric phosphatase inhibitors
Ralf Schneider, Claudia Beumer, Jeffrey R Simard, et al.
Chemical Communications (Cambridge, England)
|
October 9, 2018
Direct monitoring of the conformational equilibria of the activation loop in the mitogen-activated protein kinase p38α
Patrick Roser, Jörn Weisner, Jeffrey R Simard, et al.
Nanotechnology
|
August 13, 2011
Effect of doping- and field-induced charge carrier density on the electron transport in nanocrystalline ZnO
Maria S Hammer, Daniel Rauh, Volker Lorrmann, et al.
Page
of 16
Search research articles
Search
Showing results (31-40 of 159) with videos related to
Sort By:
Page
of 16
Biological Chemistry
|
November 20, 2002
Trypsin mutants for structure-based drug design: expression, refolding and crystallisation
Daniel Rauh, Sabine Reyda, Gerhard Klebe, et al.
The Journal of Biological Chemistry
|
October 2, 2008
Human carbonyl reductase 1 is an S-nitrosoglutathione reductase
Raynard L Bateman, Daniel Rauh, Brandon Tavshanjian, et al.
RSC Medicinal Chemistry
|
January 22, 2021
KRasG12C inhibitors in clinical trials: a short historical perspective
Lisa Goebel, Matthias P Müller, Roger S Goody, et al.
Current Opinion in Chemical Biology
|
May 5, 2009
The therapeutic potential of phosphatase inhibitors
Viktor V Vintonyak, Andrey P Antonchick, Daniel Rauh, et al.
Chemical Communications (Cambridge, England)
|
August 5, 2020
Conformational selection vs. induced fit: insights into the binding mechanisms of p38α MAP Kinase inhibitors
Patrick Roser, Jörn Weisner, Juliane Stehle, et al.
Angewandte Chemie (International Ed. in English)
|
August 24, 2017
Covalent Lipid Pocket Ligands Targeting p38α MAPK Mutants
Mike Bührmann, Julia Hardick, Jörn Weisner, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)
|
February 16, 2023
Insights into the Conformational Plasticity of the Protein Kinase Akt1 by Multi-Lateral Dipolar Spectroscopy
Juliane Stehle, Jörn Weisner, Leanne Eichhorn, et al.
Journal of the American Chemical Society
|
April 25, 2013
Selective detection of allosteric phosphatase inhibitors
Ralf Schneider, Claudia Beumer, Jeffrey R Simard, et al.
Chemical Communications (Cambridge, England)
|
October 9, 2018
Direct monitoring of the conformational equilibria of the activation loop in the mitogen-activated protein kinase p38α
Patrick Roser, Jörn Weisner, Jeffrey R Simard, et al.
Nanotechnology
|
August 13, 2011
Effect of doping- and field-induced charge carrier density on the electron transport in nanocrystalline ZnO
Maria S Hammer, Daniel Rauh, Volker Lorrmann, et al.
Page
of 16