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Journal of Chromatography. A
|
December 4, 2022
Preparation of miniaturized hydrophilic affinity monoliths: Towards a reduction of non-specific interactions and an increased target protein density
Julie Gil, Isabelle Krimm, Vincent Dugas, et al.
Photosynthesis Research
|
November 8, 2006
Protein-protein interactions within peroxiredoxin systems
Valérie Noguera-Mazon, Isabelle Krimm, Olivier Walker, et al.
Journal of Chemical Information and Modeling
|
October 31, 2014
Performance of protein-ligand docking with simulated chemical shift perturbations
Tim Ten Brink, Clémentine Aguirre, Thomas E Exner, et al.
Journal of Medicinal Chemistry
|
June 26, 2010
Ligand specificity in fragment-based drug design
Sarah Barelier, Julien Pons, Kalle Gehring, et al.
Photosynthesis Research
|
December 6, 2005
NMR of redox proteins of plants, yeasts and photosynthetic bacteria
Xavier Trivelli, Sandrine Bouillac, Pascale Tsan, et al.
Expert Opinion on Drug Discovery
|
July 19, 2023
Linkers in fragment-based drug design: an overview of the literature
Dylan Grenier, Solène Audebert, Jordane Preto, et al.
Journal of Medicinal Chemistry
|
March 3, 2010
Fragment-based deconstruction of Bcl-xL inhibitors
Sarah Barelier, Julien Pons, Olivier Marcillat, et al.
Plos One
|
July 16, 2014
Comparing binding modes of analogous fragments using NMR in fragment-based drug design: application to PRDX5
Clémentine Aguirre, Tim ten Brink, Jean-François Guichou, et al.
Journal of Biomolecular NMR
|
September 27, 2014
Protein-ligand structure guided by backbone and side-chain proton chemical shift perturbations
Clémentine Aguirre, Tim ten Brink, Olivier Cala, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry
|
January 18, 2023
Combining nano-differential scanning fluorimetry and microscale thermophoresis to investigate VDAC1 interaction with small molecules
Hubert Gorny, Angélique Mularoni, Jean-Guy Delcros, et al.
Page
of 6
Search research articles
Search
Showing results (11-20 of 52) with videos related to
Sort By:
Page
of 6
Journal of Chromatography. A
|
December 4, 2022
Preparation of miniaturized hydrophilic affinity monoliths: Towards a reduction of non-specific interactions and an increased target protein density
Julie Gil, Isabelle Krimm, Vincent Dugas, et al.
Photosynthesis Research
|
November 8, 2006
Protein-protein interactions within peroxiredoxin systems
Valérie Noguera-Mazon, Isabelle Krimm, Olivier Walker, et al.
Journal of Chemical Information and Modeling
|
October 31, 2014
Performance of protein-ligand docking with simulated chemical shift perturbations
Tim Ten Brink, Clémentine Aguirre, Thomas E Exner, et al.
Journal of Medicinal Chemistry
|
June 26, 2010
Ligand specificity in fragment-based drug design
Sarah Barelier, Julien Pons, Kalle Gehring, et al.
Photosynthesis Research
|
December 6, 2005
NMR of redox proteins of plants, yeasts and photosynthetic bacteria
Xavier Trivelli, Sandrine Bouillac, Pascale Tsan, et al.
Expert Opinion on Drug Discovery
|
July 19, 2023
Linkers in fragment-based drug design: an overview of the literature
Dylan Grenier, Solène Audebert, Jordane Preto, et al.
Journal of Medicinal Chemistry
|
March 3, 2010
Fragment-based deconstruction of Bcl-xL inhibitors
Sarah Barelier, Julien Pons, Olivier Marcillat, et al.
Plos One
|
July 16, 2014
Comparing binding modes of analogous fragments using NMR in fragment-based drug design: application to PRDX5
Clémentine Aguirre, Tim ten Brink, Jean-François Guichou, et al.
Journal of Biomolecular NMR
|
September 27, 2014
Protein-ligand structure guided by backbone and side-chain proton chemical shift perturbations
Clémentine Aguirre, Tim ten Brink, Olivier Cala, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry
|
January 18, 2023
Combining nano-differential scanning fluorimetry and microscale thermophoresis to investigate VDAC1 interaction with small molecules
Hubert Gorny, Angélique Mularoni, Jean-Guy Delcros, et al.
Page
of 6