Structural and functional evaluation of branched myofibers lacking intermediate filaments

Physiology, structure, and susceptibility to injury of skeletal muscle in mice lacking keratin 19-based and desmin-based intermediate filaments

(2011) Richard M. Lovering et al.   AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY

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

(2011) S. Chan et al.   EXPERIMENTAL PHYSIOLOGY

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

(2010) O. Friedrich et al.   BIOPHYSICAL JOURNAL

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

Mechanical and Electrophysiological Properties of the Sarcolemma of Muscle Fibers in Two Murine Models of Muscle Dystrophy: Col6a1−/−and Mdx

(2010) M. Canato et al.   JOURNAL OF BIOMEDICINE AND BIOTECHNOLOGY

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

Mammalian animal models for Duchenne muscular dystrophy

(2009) Raffaella Willmann et al.   NEUROMUSCULAR DISORDERS

Comparison of the myoplasmic calcium transient elicited by an action potential in intact fibres ofmdxand normal mice

(2008) Stephen Hollingworth et al.   JOURNAL OF PHYSIOLOGY-LONDON

Enhanced Excitation-Coupled Calcium Entry in Myotubes Expressing Malignant Hyperthermia Mutation R163C Is Attenuated by Dantrolene

(2008) G. Cherednichenko et al.   MOLECULAR PHARMACOLOGY

Muscle-specific overexpression of IGF-I improves E-C coupling in skeletal muscle fibers from dystrophic mdx mice

(2007) Jonathan D. Schertzer et al.   AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY