Odile Broux

Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A

Isabelle Richard, Odile Broux, Valéerie Allamand et al. · Cell · 1995 · 989 citations · Full text

Molecular Physiology, Skeletal Muscle, Genetics +2

β–sarcoglycan: characterization and role in limb–girdle muscular dystrophy linked to 4q12

Leland E. Lim, Franck Duclos, Odile Broux et al. · Nature Genetics · 1995 · 447 citations

Mechanobiology, Skeletal Muscle, Pathology +3

TNF-α and IL-1β inhibit RUNX2 and collagen expression but increase alkaline phosphatase activity and mineralization in human mesenchymal stem cells

Jie Ding, Olfa Ghali, P. Lencel et al. · Life Sciences · 2009 · 216 citations

Regenerative Medicine, Inflammation, Alkaline Phosphatase Activity +11

A gene for limb-girdle muscular dystrophy maps to chromosome 15 by linkage.

J. Beckmann, Isabelle Richard, Dominique Hillaire et al. · PubMed · 1991 · 152 citations

Genetics, Genetic Epidemiology, Molecular Genetics +17

A biochemical, genetic, and clinical survey of autosomal recessive limb girdle muscular dystrophies in Turkey

Pervin Dinçer, France Leturcq, Isabelle Richard et al. · Annals of Neurology · 1997 · 120 citations