Prevention of muscular dystrophy in mice by CRISPR/Cas9–mediated editing of germline DNA | Science
Inhibition of FLT1 ameliorates muscular dystrophy phenotype by increased vasculature in a mouse model of Duchenne muscular dystrophy | PLOS Genetics
Correction of Three Prominent Mutations in Mouse and Human Models of Duchenne Muscular Dystrophy by Single-Cut Genome Editing: Molecular Therapy
JCI - microRNA-206 promotes skeletal muscle regeneration and delays progression of Duchenne muscular dystrophy in mice
Whole-body clearing, staining and screening of calcium deposits in the mdx mouse model of Duchenne muscular dystrophy | Skeletal Muscle | Full Text
Muscular dystrophy research using the mdx mouse
mdx | Animal Resources Centre
Humanizing the mdx mouse model of DMD: the long and the short of it | npj Regenerative Medicine
001801 - mdx Strain Details
Full-length dystrophin restoration via targeted exon integration by AAV-CRISPR in a humanized mouse model of Duchenne muscular dystrophy: Molecular Therapy
PTEN Inhibition Ameliorates Muscle Degeneration and Improves Muscle Function in a Mouse Model of Duchenne Muscular Dystrophy | bioRxiv
Frontiers | Circadian Genes as Exploratory Biomarkers in DMD: Results From Both the mdx Mouse Model and Patients
A humanized knockin mouse model of Duchenne muscular dystrophy and its correction by CRISPR-Cas9 therapeutic gene editing - ScienceDirect
Graphical representation showing the effects of cannabinoids in mdx mice. | Download Scientific Diagram
Humanizing the mdx mouse model of DMD: the long and the short of it | npj Regenerative Medicine
Murine models of Duchenne muscular dystrophy: is there a best model? | American Journal of Physiology-Cell Physiology
Utrophin Compensates dystrophin Loss during Mouse Spermatogenesis | Scientific Reports
Postnatal genome editing partially restores dystrophin expression in a mouse model of muscular dystrophy | Science
Akt1 activation increases muscle mass in mdx mice. (A) Timeline of... | Download Scientific Diagram
Models for Muscular Dystrophy Studies | Charles River
Monitoring disease activity noninvasively in the mdx model of Duchenne muscular dystrophy | PNAS
GLPG0492, a novel selective androgen receptor modulator, improves muscle performance in the exercised-mdx mouse model of muscular dystrophy - ScienceDirect
El Entrenamiento de Baja Intensidad Provoca Adaptaciones en la Fibrosis Muscular de un Modelo de Distrofia Muscular
Cardiac Protection after Systemic Transplant of Dystrophin Expressing Chimeric (DEC) Cells to the mdx Mouse Model of Duchenne Muscular Dystrophy | SpringerLink
Voluntary wheel running complements microdystrophin gene therapy to improve muscle function in mdx mice: Molecular Therapy - Methods & Clinical Development
