Rescue of Dystrophic Skeletal Muscle by PGC-1α Involves a Fast to Slow Fiber Type Shift in the mdx Mouse

Proteomic assessment of the acute phase of dystrophin deficiency in mdx mice

(2011) D. Gardan-Salmon et al.   EUROPEAN JOURNAL OF APPLIED PHYSIOLOGY

Leupeptin-based inhibitors do not improve the mdx phenotype

(2010) Joshua Selsby et al.   AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY

Increased catalase expression improves muscle function inmdxmice

(2010) Joshua T. Selsby   EXPERIMENTAL PHYSIOLOGY

Bowman-Birk inhibitor attenuates dystrophic pathology in mdx mice

(2010) C. A. Morris et al.   JOURNAL OF APPLIED PHYSIOLOGY

Restoration of γ-Sarcoglycan Localization and Mechanical Signal Transduction Are Independent in Murine Skeletal Muscle

(2010) Elisabeth R. Barton   JOURNAL OF BIOLOGICAL CHEMISTRY

Activin IIB receptor blockade attenuates dystrophic pathology in a mouse model of duchenne muscular dystrophy

(2010) Kevin J. Morine et al.   MUSCLE & NERVE

Muscular dystrophy begins early in embryonic development deriving from stem cell loss and disrupted skeletal muscle formation

(2009) D. Merrick et al.   Disease Models & Mechanisms

Pharmacological activation of PPAR /  stimulates utrophin A expression in skeletal muscle fibers and restores sarcolemmal integrity in mature mdx mice

(2009) P. Miura et al.   HUMAN MOLECULAR GENETICS

Clinical approaches in the treatment of Duchenne muscular dystrophy (DMD) using oligonucleotides

(2007) Carmen Bertoni   Frontiers in Bioscience-Landmark

Effective Exon Skipping and Restoration of Dystrophin Expression by Peptide Nucleic Acid Antisense Oligonucleotides in mdx Mice

(2007) Haifang Yin et al.   MOLECULAR THERAPY