acetylcysteine and Muscular Dystrophy, Animal

acetylcysteine has been researched along with Muscular Dystrophy, Animal in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (50.00)29.6817
2010's2 (50.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Boittin, FX; Dorchies, OM; Patthey-Vuadens, O; Reutenauer-Patte, J; Ruegg, UT1
Arthur, PG; Grounds, MD; Radley-Crabb, HG; Terrill, JR1
Allen, DG; Gervasio, OL; Pham, C; Whitehead, NP1
Reggiani, C1

Other Studies

4 other study(ies) available for acetylcysteine and Muscular Dystrophy, Animal

ArticleYear
Urocortins improve dystrophic skeletal muscle structure and function through both PKA- and Epac-dependent pathways.
    The American journal of pathology, 2012, Volume: 180, Issue:2

    Topics: Acetylcysteine; Animals; Brefeldin A; Calcium; Calcium Channels; Cyclic AMP-Dependent Protein Kinases; Erythromycin; Group VI Phospholipases A2; Injections, Intradermal; Membrane Glycoproteins; Mice; Mice, Inbred C57BL; Muscle Contraction; Muscle Relaxation; Muscle Strength; Muscle, Skeletal; Muscular Dystrophy, Animal; Protein Kinase Inhibitors; Protein Synthesis Inhibitors; Receptors, Corticotropin-Releasing Hormone; Stromal Interaction Molecule 1; Urocortins

2012
N-Acetylcysteine treatment of dystrophic mdx mice results in protein thiol modifications and inhibition of exercise induced myofibre necrosis.
    Neuromuscular disorders : NMD, 2012, Volume: 22, Issue:5

    Topics: Acetylcysteine; Animals; Antioxidants; Glutathione; Male; Mice; Mice, Inbred C57BL; Mice, Inbred mdx; Muscle, Skeletal; Muscular Dystrophy, Animal; Necrosis; Oxidative Stress; Physical Conditioning, Animal; Protein Carbonylation; Proteins; Sulfhydryl Compounds

2012
N-Acetylcysteine ameliorates skeletal muscle pathophysiology in mdx mice.
    The Journal of physiology, 2008, Apr-01, Volume: 586, Issue:7

    Topics: Acetylcysteine; Animals; Caveolin 3; Disease Models, Animal; Dystroglycans; Dystrophin; Free Radical Scavengers; Mice; Mice, Inbred mdx; Muscle Contraction; Muscle, Skeletal; Muscular Dystrophy, Animal; Muscular Dystrophy, Duchenne; Mutation; NF-kappa B; Reactive Oxygen Species

2008
Between channels and tears: aim at ROS to save the membrane of dystrophic fibres.
    The Journal of physiology, 2008, Apr-01, Volume: 586, Issue:7

    Topics: Acetylcysteine; Animals; Caveolin 3; Disease Models, Animal; Dystroglycans; Dystrophin; Free Radical Scavengers; Mice; Mice, Inbred mdx; Mitochondria, Muscle; Muscle Fibers, Skeletal; Muscle, Skeletal; Muscular Dystrophy, Animal; Muscular Dystrophy, Duchenne; Mutation; Reactive Oxygen Species

2008