Nathalie Bourg

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

Isabelle Richard, Odile Broux, Valéerie Allamand et al. · Cell · 1995 · 997 citations · Full text

Life Sciences, Genetics, Molecular Biology +11

A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B

Rumaisa Bashir, S. Britton, Tom Strachan et al. · Nature Genetics · 1998 · 683 citations

Medicine, Genetics, Molecular Genetics +11

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 · 449 citations

Medicine, Biochemistry, Molecular Biology +10

Calpain 3 deficiency is associated with myonuclear apoptosis and profound perturbation of the IκBα/NF-κB pathway in limb-girdle muscular dystrophy type 2A

Stephen Baghdiguian, Marianne Martin, Françoise Pons et al. · Nature Medicine · 1999 · 276 citations

Life Sciences, Cell Biology, Pathology +10

Loss of Calpain 3 Proteolytic Activity Leads to Muscular Dystrophy and to Apoptosis-Associated Iκbα/Nuclear Factor κb Pathway Perturbation in Mice

Carinne Roudaut, Sylvie Marchand, Stephen Baghdiguian et al. · The Journal of Cell Biology · 2000 · 174 citations · Full text

Medicine, Genetics, Molecular Genetics +14