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Sarah Barelier

Showing results (1-10 of 18) with videos related to

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Current Opinion in Chemical Biology|March 18, 2011
Ligand specificity, privileged substructures and protein druggability from fragment-based screeningSarah Barelier, Isabelle Krimm
Structure (London, England : 1993)|October 7, 2022
The long-awaited structure of human fucosidase FucA1 opens novel avenues for the treatment of fucosidosisSarah Barelier, Gerlind Sulzenbacher
ACS Chemical Biology|October 1, 2015
The Recognition of Identical Ligands by Unrelated ProteinsSarah Barelier, Teague Sterling, Matthew J O'Meara, et al.
Journal of Medicinal Chemistry|June 26, 2010
Ligand specificity in fragment-based drug designSarah Barelier, Julien Pons, Kalle Gehring, et al.
Journal of Medicinal Chemistry|March 3, 2010
Fragment-based deconstruction of Bcl-xL inhibitorsSarah Barelier, Julien Pons, Olivier Marcillat, et al.
Biochemical and Biophysical Research Communications|August 31, 2010
The role of the glycine triad in human glutathione synthetaseAdriana Dinescu, Teresa R Brown, Sarah Barelier, et al.
Nucleic Acids Research|April 30, 2024
ChemoDOTS: a web server to design chemistry-driven focused librariesLaurent Hoffer, Guillaume Charifi-Hoareau, Sarah Barelier, et al.
Plos One|July 23, 2013
Roles for ordered and bulk solvent in ligand recognition and docking in two related cavitiesSarah Barelier, Sarah E Boyce, Inbar Fish, et al.
Plos One|March 23, 2010
Discovery of fragment molecules that bind the human peroxiredoxin 5 active siteSarah Barelier, Dominique Linard, Julien Pons, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 9, 2012
Fragment-guided design of subnanomolar β-lactamase inhibitors active in vivoOliv Eidam, Chiara Romagnoli, Guillaume Dalmasso, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
Current Opinion in Chemical Biology|March 18, 2011
Ligand specificity, privileged substructures and protein druggability from fragment-based screeningSarah Barelier, Isabelle Krimm
Structure (London, England : 1993)|October 7, 2022
The long-awaited structure of human fucosidase FucA1 opens novel avenues for the treatment of fucosidosisSarah Barelier, Gerlind Sulzenbacher
ACS Chemical Biology|October 1, 2015
The Recognition of Identical Ligands by Unrelated ProteinsSarah Barelier, Teague Sterling, Matthew J O'Meara, et al.
Journal of Medicinal Chemistry|June 26, 2010
Ligand specificity in fragment-based drug designSarah Barelier, Julien Pons, Kalle Gehring, et al.
Journal of Medicinal Chemistry|March 3, 2010
Fragment-based deconstruction of Bcl-xL inhibitorsSarah Barelier, Julien Pons, Olivier Marcillat, et al.
Biochemical and Biophysical Research Communications|August 31, 2010
The role of the glycine triad in human glutathione synthetaseAdriana Dinescu, Teresa R Brown, Sarah Barelier, et al.
Nucleic Acids Research|April 30, 2024
ChemoDOTS: a web server to design chemistry-driven focused librariesLaurent Hoffer, Guillaume Charifi-Hoareau, Sarah Barelier, et al.
Plos One|July 23, 2013
Roles for ordered and bulk solvent in ligand recognition and docking in two related cavitiesSarah Barelier, Sarah E Boyce, Inbar Fish, et al.
Plos One|March 23, 2010
Discovery of fragment molecules that bind the human peroxiredoxin 5 active siteSarah Barelier, Dominique Linard, Julien Pons, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 9, 2012
Fragment-guided design of subnanomolar β-lactamase inhibitors active in vivoOliv Eidam, Chiara Romagnoli, Guillaume Dalmasso, et al.
Pageof 2