Prevention of muscular dystrophy in mice by CRISPR/Cas9–mediated editing of germline DNA | Science
Voluntary wheel running complements microdystrophin gene therapy to improve muscle function in mdx mice: Molecular Therapy - Methods & Clinical Development
A humanized knockin mouse model of Duchenne muscular dystrophy and its correction by CRISPR-Cas9 therapeutic gene editing - ScienceDirect
Utrophin Compensates dystrophin Loss during Mouse Spermatogenesis | Scientific Reports
Monitoring disease activity noninvasively in the mdx model of Duchenne muscular dystrophy | PNAS
mdx | Animal Resources Centre
Correction of Three Prominent Mutations in Mouse and Human Models of Duchenne Muscular Dystrophy by Single-Cut Genome Editing: Molecular Therapy
The Importance of Animal Experimentation and the mdx mouse model to Muscular Dystrophy Research – Speaking of Research
Humanizing the mdx mouse model of DMD: the long and the short of it | npj Regenerative Medicine
Peptide-conjugated phosphodiamidate oligomer-mediated exon skipping has benefits for cardiac function in mdx and Cmah-/-mdx mouse models of Duchenne muscular dystrophy | PLOS ONE
Assessing functional performance in the mdx mouse model. - Abstract - Europe PMC
JCI - microRNA-206 promotes skeletal muscle regeneration and delays progression of Duchenne muscular dystrophy in mice
Mouse Models of Duchenne Muscular Dystrophy (DMD) - Aurora Scientific
Humanizing the mdx mouse model of DMD: the long and the short of it | npj Regenerative Medicine
El Entrenamiento de Baja Intensidad Provoca Adaptaciones en la Fibrosis Muscular de un Modelo de Distrofia Muscular
Murine models of Duchenne muscular dystrophy: is there a best model? | American Journal of Physiology-Cell Physiology
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
Treatment with human immunoglobulin G improves the early disease course in a mouse model of Duchenne muscular dystrophy - Zschüntzsch - 2016 - Journal of Neurochemistry - Wiley Online Library
The D2.mdx mouse as a preclinical model of the skeletal muscle pathology associated with Duchenne muscular dystrophy | Scientific Reports
Cardiac Protection after Systemic Transplant of Dystrophin Expressing Chimeric (DEC) Cells to the mdx Mouse Model of Duchenne Muscular Dystrophy | SpringerLink
Akt1 activation increases muscle mass in mdx mice. (A) Timeline of... | Download Scientific Diagram
Social stress is lethal in the mdx model of Duchenne muscular dystrophy - eBioMedicine
