Properties of regenerated mouse extensor digitorum longus muscle following notexin injury

The role of branched fibres in the pathogenesis of Duchenne muscular dystrophy

(2011) S. Chan et al.   EXPERIMENTAL PHYSIOLOGY

Elevated levels of active matrix metalloproteinase-9 cause hypertrophy in skeletal muscle of normal and dystrophin-deficient mdx mice

(2011) Saurabh Dahiya et al.   HUMAN MOLECULAR GENETICS

The passive mechanical properties of the extensor digitorum longus muscle are compromised in 2- to 20-mo-old mdx mice

(2011) Chady H. Hakim et al.   JOURNAL OF APPLIED PHYSIOLOGY

Microarchitecture Is Severely Compromised but Motor Protein Function Is Preserved in Dystrophic mdx Skeletal Muscle

(2010) O. Friedrich et al.   BIOPHYSICAL JOURNAL

Calcium and the damage pathways in muscular dystrophyThis article is one of a selection of papers published in this special issue on Calcium Signaling.

(2010) David G. Allen et al.   CANADIAN JOURNAL OF PHYSIOLOGY AND PHARMACOLOGY

Branched fibres in old dystrophicmdxmuscle are associated with mechanical weakening of the sarcolemma, abnormal Ca2+transients and a breakdown of Ca2+homeostasis during fatigue

(2010) Stewart I. Head   EXPERIMENTAL PHYSIOLOGY

Malformed mdx myofibers have normal cytoskeletal architecture yet altered EC coupling and stress-induced Ca2+ signaling

(2009) Richard M. Lovering et al.   AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY