duchenne muscular dystrophy and glutathione Evaluation of the redox alteration in model mice using in vivo DNP-MRI Mitochondrial creatine sensitivity is lost

Mitochondrial creatine sensitivity is lost in the D2.mdx model of Duchenne muscular dystrophy and rescued by the mitochondrial enhancing compound Olesoxime American Journal of Physiology Cell Physiology American Physiological Society The role of fibrosis in the pathophysiology of muscular dystrophy American Journal of Physiology Cell Physiology American Physiological Society Dynamic responses of the glutathione system to acute oxidative stress in dystrophic mouse (mdx) muscles American Journal of Physiology Regulatory, Integrative and Comparative Physiology American Physiological Society Duchenne Muscular Dystrophy YouTube

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