Murine models of Duchenne muscular dystrophy: is there a best model? | American Journal of Physiology-Cell Physiology
In vivo non-invasive monitoring of dystrophin correction in a new Duchenne muscular dystrophy reporter mouse | Nature Communications
Whole-body clearing, staining and screening of calcium deposits in the mdx mouse model of Duchenne muscular dystrophy | Skeletal Muscle | Full Text
JCI Insight - Micro-dystrophin gene therapy prevents heart failure in an improved Duchenne muscular dystrophy cardiomyopathy mouse model
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
Cardiac Protection after Systemic Transplant of Dystrophin Expressing Chimeric (DEC) Cells to the mdx Mouse Model of Duchenne Muscular Dystrophy | SpringerLink
JCI Insight - Duchenne muscular dystrophy hiPSC–derived myoblast drug screen identifies compounds that ameliorate disease in mdx mice
Cardiac Myoediting Attenuates Cardiac Abnormalities in Human and Mouse Models of Duchenne Muscular Dystrophy | Circulation Research
001801 - mdx Strain Details
Rodent Duchenne Muscular Dystrophy (DMD) Model - Creative Biolabs
Phenotypic characterization of the Dmd / Large mouse: (A) Growth and... | Download Scientific Diagram
Synthesis of SMT022357 enantiomers and in vivo evaluation in a Duchenne muscular dystrophy mouse model - ScienceDirect
Models for Muscular Dystrophy Studies | Charles River
Full-length dystrophin restoration via targeted exon integration by AAV-CRISPR in a humanized mouse model of Duchenne muscular dystrophy: Molecular Therapy
Mouse Models of Duchenne Muscular Dystrophy (DMD) - Aurora Scientific
Tamoxifen ameliorates symptoms of Duchenne mu | EurekAlert!
Duchenne's muscular dystrophy involves a defective transsulfuration pathway activity - ScienceDirect
Deleting Mss51 Gene in DMD Mice Eases Fatigue, Increases Endurance
Representative animal models for DMD. (A) Representative pictures of... | Download Scientific Diagram
Stem Cell–Derived Cardiomyocytes and Beta-Adrenergic Receptor Blockade in Duchenne Muscular Dystrophy Cardiomyopathy - ScienceDirect
VEGFR-1/Flt-1 inhibition increases angiogenesis and improves muscle function in a mouse model of Duchenne muscular dystrophy: Molecular Therapy - Methods & Clinical Development
PTEN Inhibition Ameliorates Muscle Degeneration and Improves Muscle Function in a Mouse Model of Duchenne Muscular Dystrophy | bioRxiv
Penn developed Gene Therapy for Duchenne Muscular Dystrophy Safely Preserves Muscle Function – REGENHEALTHSOLUTIONS (RHS)
El Entrenamiento de Baja Intensidad Provoca Adaptaciones en la Fibrosis Muscular de un Modelo de Distrofia Muscular
Prevention of muscular dystrophy in mice by CRISPR/Cas9–mediated editing of germline DNA | Science
Animal model choice for DMD - TREAT-NMD
Monitoring disease activity noninvasively in the mdx model of Duchenne muscular dystrophy | PNAS
