A Morpholino Oligomer Therapy Regime That Restores Mitochondrial Function and Prevents mdx Cardiomyopathy | JACC: Basic to Translational Science
Phenotypic characterization of the Dmd / Large mouse: (A) Growth and... | Download Scientific Diagram
Moderate exercise improves function and increases adiponectin in the mdx mouse model of muscular dystrophy | Scientific Reports
Humanizing the mdx mouse model of DMD: the long and the short of it | npj Regenerative Medicine
The D2.mdx mouse as a preclinical model of the skeletal muscle pathology associated with Duchenne muscular dystrophy | Scientific Reports
Duchenne Muscular Dystrophy Models | Charles River
538. Transgenic Mini-Dystrophin Expression in Skeletal Muscles of Mdx:utrn-/- Double KO Mice Ameliorates Dystrophic Phenotypes and Remarkably Extends Life Span: Molecular Therapy
Muscular dystrophy research using the mdx mouse
Whole-body clearing, staining and screening of calcium deposits in the mdx mouse model of Duchenne muscular dystrophy | Skeletal Muscle | Full Text
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
Correction of Three Prominent Mutations in Mouse and Human Models of Duchenne Muscular Dystrophy by Single-Cut Genome Editing: Molecular Therapy
Frontiers | Oxidative Stress, Inflammation, and Activators of Mitochondrial Biogenesis: Tempol Targets in the Diaphragm Muscle of Exercise Trained-mdx Mice
![IJMS | Free Full-Text | A Protocol for Simultaneous In Vivo Imaging of Cardiac and Neuroinflammation in Dystrophin-Deficient MDX Mice Using [18F]FEPPA PET](https://www.mdpi.com/ijms/ijms-24-07522/article_deploy/html/images/ijms-24-07522-g001.png "IJMS | Free Full-Text | A Protocol for Simultaneous In Vivo Imaging of Cardiac and Neuroinflammation in Dystrophin-Deficient MDX Mice Using [18F]FEPPA PET")
IJMS | Free Full-Text | A Protocol for Simultaneous In Vivo Imaging of Cardiac and Neuroinflammation in Dystrophin-Deficient MDX Mice Using [18F]FEPPA PET
Resveratrol Ameliorates Muscular Pathology in the Dystrophic mdx Mouse, a Model for Duchenne Muscular Dystrophy | Journal of Pharmacology and Experimental Therapeutics
Stem Cell–Derived Cardiomyocytes and Beta-Adrenergic Receptor Blockade in Duchenne Muscular Dystrophy Cardiomyopathy - ScienceDirect
Utrophin-Dystrophin-Deficient Mice as a Model for Duchenne Muscular Dystrophy: Cell
Social stress is lethal in the mdx model of Duchenne muscular dystrophy - eBioMedicine
GLPG0492, a novel selective androgen receptor modulator, improves muscle performance in the exercised-mdx mouse model of muscular dystrophy - ScienceDirect
001801 - mdx Strain Details
IJMS | Free Full-Text | Microdystrophin Gene Addition Significantly Improves Muscle Functionality and Diaphragm Muscle Histopathology in a Fibrotic Mouse Model of Duchenne Muscular Dystrophy
Voluntary wheel running complements microdystrophin gene therapy to improve muscle function in mdx mice: Molecular Therapy - Methods & Clinical Development
Full-length dystrophin restoration via targeted exon integration by AAV-CRISPR in a humanized mouse model of Duchenne muscular dystrophy: Molecular Therapy
Muscle Structure Influences Utrophin Expression in mdx Mice | PLOS Genetics
JCI Insight - Lack of miR-378 attenuates muscular dystrophy in mdx mice
