Murine models of Duchenne muscular dystrophy: is there a best model? | American Journal of Physiology-Cell Physiology
Duchenne Muscular Dystrophy Models | Charles River
Prevention of muscular dystrophy in mice by CRISPR/Cas9–mediated editing of germline DNA | Science
Full-length dystrophin restoration via targeted exon integration by AAV-CRISPR in a humanized mouse model of Duchenne muscular dystrophy: Molecular Therapy
Mechanics of dystrophin deficient skeletal muscles in very young mice and effects of age | American Journal of Physiology-Cell Physiology
PTEN Inhibition Ameliorates Muscle Degeneration and Improves Muscle Function in a Mouse Model of Duchenne Muscular Dystrophy | bioRxiv
Cardiac Protection after Systemic Transplant of Dystrophin Expressing Chimeric (DEC) Cells to the mdx Mouse Model of Duchenne Muscular Dystrophy | SpringerLink
Early manifestation of alteration in cardiac function in dystrophin deficient mdx mouse using 3D CMR tagging | Journal of Cardiovascular Magnetic Resonance | Full Text
pGz increases muscle strength and reduces muscle damage in mdx mice.
The D2.mdx mouse as a preclinical model of the skeletal muscle pathology associated with Duchenne muscular dystrophy | Scientific Reports
Humanizing the mdx mouse model of DMD: the long and the short of it | npj Regenerative Medicine
001801 - mdx Strain Details
Mouse Models of Duchenne Muscular Dystrophy (DMD) - Aurora Scientific
Enhanced Arteriogenesis and Wound Repair in Dystrophin-Deficient mdx Mice | Circulation
The Importance of Animal Experimentation and the mdx mouse model to Muscular Dystrophy Research – Speaking of Research
The D2.mdx mouse as a preclinical model of the skeletal muscle pathology associated with Duchenne muscular dystrophy | Scientific Reports
Life | Free Full-Text | Deficiency of MMP-10 Aggravates the Diseased Phenotype of Aged Dystrophic Mice
chromocenter Web Page
Humanizing the mdx mouse model of DMD: the long and the short of it | npj Regenerative Medicine
JCI Insight - Myocyte-derived Myomaker expression is required for regenerative fusion but exacerbates membrane instability in dystrophic myofibers
Micro-utrophin Improves Cardiac and Skeletal Muscle Function of Severely Affected D2/mdx Mice: Molecular Therapy - Methods & Clinical Development
