Muscular dystrophy research using the mdx mouse
The D2.mdx mouse as a preclinical model of the skeletal muscle pathology associated with Duchenne muscular dystrophy | Scientific Reports
mdx | Animal Resources Centre
Frontiers | Circadian Genes as Exploratory Biomarkers in DMD: Results From Both the mdx Mouse Model and Patients
Correction of Three Prominent Mutations in Mouse and Human Models of Duchenne Muscular Dystrophy by Single-Cut Genome Editing: Molecular Therapy
Models for Muscular Dystrophy Studies | Charles River
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
Dystropathology Increases Energy Expenditure and Protein Turnover in the Mdx Mouse Model of Duchenne Muscular Dystrophy | PLOS ONE
Mouse Models of Duchenne Muscular Dystrophy (DMD) - Aurora Scientific
Akt1 activation increases muscle mass in mdx mice. (A) Timeline of... | Download Scientific Diagram
Voluntary wheel running complements microdystrophin gene therapy to improve muscle function in mdx mice: Molecular Therapy - Methods & Clinical Development
VEGFR-1/Flt-1 inhibition increases angiogenesis and improves muscle function in a mouse model of Duchenne muscular dystrophy: Molecular Therapy - Methods & Clinical Development
Monitoring disease activity noninvasively in the mdx model of Duchenne muscular dystrophy | PNAS
Graphical representation showing the effects of cannabinoids in mdx mice. | Download Scientific Diagram
PTEN Inhibition Ameliorates Muscle Degeneration and Improves Muscle Function in a Mouse Model of Duchenne Muscular Dystrophy | bioRxiv
The Importance of Animal Experimentation and the mdx mouse model to Muscular Dystrophy Research – Speaking of Research
Prevention of muscular dystrophy in mice by CRISPR/Cas9–mediated editing of germline DNA | Science
El Entrenamiento de Baja Intensidad Provoca Adaptaciones en la Fibrosis Muscular de un Modelo de Distrofia Muscular
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
chromocenter Web Page
A Morpholino Oligomer Therapy Regime That Restores Mitochondrial Function and Prevents mdx Cardiomyopathy | JACC: Basic to Translational Science
JCI - microRNA-206 promotes skeletal muscle regeneration and delays progression of Duchenne muscular dystrophy in mice
Assessing functional performance in the mdx mouse model. - Abstract - Europe PMC
