Louise V.B. Anderson

Dysferlin is a Plasma Membrane Protein and is Expressed Early in Human Development

Louise V.B. Anderson, Kenneth Davison, Jessica Moss et al. · Human Molecular Genetics · 1999 · 292 citations

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, Isabelle Richard et al. · Nature Medicine · 1999 · 275 citations

Signal Transduction, Molecular Physiology, Skeletal Muscle +12

Calpainopathy—A Survey of Mutations and Polymorphisms

Isabelle Richard, Carinne Roudaut, Amets Sáenz et al. · The American Journal of Human Genetics · 1999 · 206 citations · Full text

Genetic Disorder, Genetics, Genetic Epidemiology +5

AHNAK a novel component of the dysferlin protein complex, redistributes to the cytoplasm with dysferlin during skeletal muscle regeneration

Yanchao Huang, Steven H. Laval, Alexandra van Remoortere et al. · The FASEB Journal · 2006 · 180 citations

Muscle Function, Cytoskeleton, Dysferlin Protein Complex +20

Identical Mutation in Patients with Limb Girdle Muscular Dystrophy Type 2B Or Miyoshi Myopathy Suggests a Role for Modifier Gene(s)

Tracey Weiler, R. Bashir, Louise V.B. Anderson et al. · Human Molecular Genetics · 1999 · 179 citations

Miyoshi Myopathy, Rare Diseases, Or Miyoshi Myopathy +13