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The Biochemical Journal|November 15, 1994
Structural comparisons lead to the definition of a new superfamily of NAD(P)(H)-accepting oxidoreductases: the single-domain reductases/epimerases/dehydrogenases (the 'RED' family)G Labesse, A Vidal-Cros, J Chomilier, et al.
FEBS Letters|March 10, 2000
MOMP (major outer membrane protein) of Campylobacter jejuni; a versatile pore-forming proteinE Dé, M Jullien, G Labesse, et al.
Biochemical and Biophysical Research Communications|February 13, 2001
MOMP, a divergent porin from Campylobacter: cloning and primary structural characterizationG Labesse, E Garnotel, S Bonnel, et al.
Biochemical and Biophysical Research Communications|May 21, 1999
Sequence analysis identifies a ras-associating (RA)-like domain in the N-termini of band 4.1/JEF domains and in the Grb7/10/14 adapter familyJ Wojcik, J A Girault, G Labesse, et al.
The Journal of Biological Chemistry|January 27, 1998
HAH1 is a copper-binding protein with distinct amino acid residues mediating copper homeostasis and antioxidant defenseI H Hung, R L Casareno, G Labesse, et al.
Proteins|December 3, 1999
Structure modelling and site-directed mutagenesis of the rat aromatic L-amino acid pyridoxal 5'-phosphate-dependent decarboxylase: a functional studyA Poupon, F Jebai, G Labesse, et al.
European Journal of Biochemistry|October 16, 1999
Characterization and molecular cloning of an adenosine kinase from Babesia canis rossiC Carret, S Delbecq, G Labesse, et al.
Cellular and Molecular Life Sciences : CMLS|August 1, 1997
Deciphering protein sequence information through hydrophobic cluster analysis (HCA): current status and perspectivesI Callebaut, G Labesse, P Durand, et al.
The Journal of Biological Chemistry|September 25, 1998
Crystallographic and spectroscopic studies of native, aminoquinol, and monovalent cation-bound forms of methylamine dehydrogenase from Methylobacterium extorquens AM1G Labesse, D Ferrari, Z W Chen, et al.
International Journal for Parasitology. Drugs and Drug Resistance|February 8, 2018
Synthesis of aminophenylhydroxamate and aminobenzylhydroxamate derivatives and in vitro screening for antiparasitic and histone deacetylase inhibitory activityC Loeuillet, B Touquet, B Oury, et al.
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