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Full-length dystrophin restoration via targeted exon integration by AAV-CRISPR in a humanized mouse model of Duchenne muscular dystrophy: Molecular Therapy
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Mechanics of dystrophin deficient skeletal muscles in very young mice and effects of age | American Journal of Physiology-Cell Physiology
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IJMS | Free Full-Text | Lipocalin 2 Influences Bone and Muscle Phenotype in the MDX Mouse Model of Duchenne Muscular Dystrophy
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Resveratrol Ameliorates Muscular Pathology in the Dystrophic mdx Mouse, a Model for Duchenne Muscular Dystrophy | Journal of Pharmacology and Experimental Therapeutics
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Functional correction of adult mdx mouse muscle using gutted adenoviral vectors expressing full-length dystrophin | PNAS
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Micro-utrophin Improves Cardiac and Skeletal Muscle Function of Severely Affected D2/mdx Mice: Molecular Therapy Methods & Clinical Development
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The D2.mdx mouse as a preclinical model of the skeletal muscle pathology associated with Duchenne muscular dystrophy | Scientific Reports
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JCI Insight - TGF-β–driven muscle degeneration and failed regeneration underlie disease onset in a DMD mouse model
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Cells | Free Full-Text | Oligonucleotide Enhancing Compound Increases Tricyclo-DNA Mediated Exon-Skipping Efficacy in the Mdx Mouse Model
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Whole-body clearing, staining and screening of calcium deposits in the mdx mouse model of Duchenne muscular dystrophy | Skeletal Muscle | Full Text
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Duchenne's muscular dystrophy involves a defective transsulfuration pathway activity - ScienceDirect
Graphical representation showing the effects of cannabinoids in mdx mice. | Download Scientific Diagram
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IJMS | Free Full-Text | A Protocol for Simultaneous In Vivo Imaging of Cardiac and Neuroinflammation in Dystrophin-Deficient MDX Mice Using [18F]FEPPA PET
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Voluntary wheel running complements microdystrophin gene therapy to improve muscle function in mdx mice - ScienceDirect
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Moderate exercise improves function and increases adiponectin in the mdx mouse model of muscular dystrophy | Scientific Reports
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