Y. Le Merrer*

Synthesis of polyhydroxylated piperidines and evaluation as glycosidase inhibitors.

Marie-Christine Lallemand, F. Tillequin, C. Gravier-Pelletier, 2004, Bioorganic & medicinal chemistry.

Synthesis and biological evaluation of a triazole-based library of pyrido[2,3-d]pyrimidines as FGFR3 tyrosine kinase inhibitors.

François Radvanyi, F. Radvanyi, J. Aubertin, 2010, Organic & biomolecular chemistry.

A novel tyrosine kinase inhibitor restores chondrocyte differentiation and promotes bone growth in a gain-of-function Fgfr3 mouse model.

Arnold Munnich, Florent Barbault, A. Munnich, 2012, Human molecular genetics.

Synthesis and biological evaluation of potential new inhibitors of the bacterial transferase MraY with a β-ketophosphonate structure.

A. Bouhss, R. Frlan, C. Gravier-Pelletier, 2011, Organic & biomolecular chemistry.

Mono, di and tri-mannopyranosyl phosphates as mannose-1-phosphate prodrugs for potential CDG-Ia therapy.

C. Gravier-Pelletier, Y. Le Merrer, T. Dupré, 2007, Bioorganic & medicinal chemistry letters.

Synthesis and biological evaluation of a diazepanone-based library of liposidomycins analogs as MraY inhibitors.

Janez Mravljak, A. Bouhss, C. Gravier-Pelletier, 2011, European journal of medicinal chemistry.

Synthesis of purin-2-yl and purin-6-yl-aminoglucitols as C-nucleosidic ATP mimics and biological evaluation as FGFR3 inhibitors.

François Maurel, Florent Barbault, Y. Le Merrer, 2011, European journal of medicinal chemistry.