Muscle-specific expression of insulin-like growth factor 1 improves outcome in Lama2(Dy-w) mice, a model for congenital muscular dystrophy type 1A

Por Kumar, Ajay, Yamauchi, Jenny, Girgenrath, Tanya, Girgenrath, Mahasweta
Publicado em 2011

Dysregulation of matricellular proteins is an early signature of pathology in laminin-deficient muscular dystrophy

Por Mehuron, Thomas, Kumar, Ajay, Duarte, Lina, Yamauchi, Jenny, Accorsi, Anthony, Girgenrath, Mahasweta
Publicado em 2014

Correction: dysregulation of matricellular proteins is an early signature of pathology in laminin-deficient muscular dystrophy

Por Mehuron, Thomas, Kumar, Ajay, Duarte, Lina, Yamauchi, Jenny, Accorsi, Anthony, Girgenrath, Mahasweta
Publicado em 2014