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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 KrimmJournal 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.Plos One|March 23, 2010
Discovery of fragment molecules that bind the human peroxiredoxin 5 active siteSarah Barelier, Dominique Linard, Julien Pons, et al.Chemmedchem|March 7, 2017
Identifying Protein Allosteric Transitions for Drug Discovery with 1D NMRIsabelle KrimmMedecine Sciences : M/S|March 7, 2015
[Fragment-based screening: a promising avenue for drug design]Isabelle KrimmStructure (London, England : 1993)|October 7, 2022
The long-awaited structure of human fucosidase FucA1 opens novel avenues for the treatment of fucosidosisSarah Barelier, Gerlind SulzenbacherPlos Computational Biology|February 12, 2021
The intrinsically disordered N-terminus of the voltage-dependent anion channelJordane Preto, Isabelle KrimmJournal of Medicinal Chemistry|October 23, 2015
Ligand-Orientation Based Fragment Selection in STD NMR ScreeningOlivier Cala, Isabelle KrimmFuture Medicinal Chemistry|July 10, 2019
NMR investigation of protein-ligand interactions for G-protein coupled receptorsClaire Raingeval, Isabelle KrimmPageof 7