PTEN Inhibition Ameliorates Muscle Degeneration and Improves Muscle Function in a Mouse Model of Duchenne Muscular Dystrophy | bioRxiv
Prevention of muscular dystrophy in mice by CRISPR/Cas9–mediated editing of germline DNA | Science
Murine models of Duchenne muscular dystrophy: is there a best model? | American Journal of Physiology-Cell Physiology
538. Transgenic Mini-Dystrophin Expression in Skeletal Muscles of Mdx:utrn-/- Double KO Mice Ameliorates Dystrophic Phenotypes and Remarkably Extends Life Span: Molecular Therapy
Graphical representation showing the effects of cannabinoids in mdx mice. | Download Scientific Diagram
A Morpholino Oligomer Therapy Regime That Restores Mitochondrial Function and Prevents mdx Cardiomyopathy | JACC: Basic to Translational Science
Mouse Models of Duchenne Muscular Dystrophy (DMD) - Aurora Scientific
Duchenne's muscular dystrophy involves a defective transsulfuration pathway activity - ScienceDirect
Mechanics of dystrophin deficient skeletal muscles in very young mice and effects of age | American Journal of Physiology-Cell Physiology
Humanizing the mdx mouse model of DMD: the long and the short of it | npj Regenerative Medicine
Whole-body clearing, staining and screening of calcium deposits in the mdx mouse model of Duchenne muscular dystrophy | Skeletal Muscle | Full Text
Life | Free Full-Text | Deficiency of MMP-10 Aggravates the Diseased Phenotype of Aged Dystrophic Mice
The D2.mdx mouse as a preclinical model of the skeletal muscle pathology associated with Duchenne muscular dystrophy | Scientific Reports
Muscle Structure Influences Utrophin Expression in mdx Mice | PLOS Genetics
JCI Insight - TGF-β–driven muscle degeneration and failed regeneration underlie disease onset in a DMD mouse model
![PDF] Commentary : SU 9516 increases α 7 β 1 Integrin and Ameliorates Disease Progression in the mdx Mouse Model of Duchenne Muscular Dystrophy | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/af5983836a603cfcb49fd97df5c2fe24f1d30b25/3-Figure1-1.png "PDF] Commentary : SU 9516 increases α 7 β 1 Integrin and Ameliorates Disease Progression in the mdx Mouse Model of Duchenne Muscular Dystrophy | Semantic Scholar")
PDF] Commentary : SU 9516 increases α 7 β 1 Integrin and Ameliorates Disease Progression in the mdx Mouse Model of Duchenne Muscular Dystrophy | Semantic Scholar
Cells | Free Full-Text | Oligonucleotide Enhancing Compound Increases Tricyclo-DNA Mediated Exon-Skipping Efficacy in the Mdx Mouse Model
JCI Insight - Lack of miR-378 attenuates muscular dystrophy in 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
Assessing Functional Performance in the Mdx Mouse Model | Protocol (Translated to Spanish)
Myofiber / pro-inflammatory macrophage interplay controls muscle damage in mdx mice | bioRxiv
miR-146a deficiency does not aggravate muscular dystrophy in mdx mice | Skeletal Muscle | Full Text
