Studies on mitochondria from dystrophic skeletal muscle of mice
Author:
Publisher
Elsevier BV
Subject
Biochemistry,Endocrinology, Diabetes and Metabolism
Reference18 articles.
1. OXIDATIVE PHOSPHORYLATION BY MUSCLE MITOCHONDRIA OF DYSTROPHIC MICE
2. Respiration and oxidative phosphorylation by muscle and heart mitochondria of hamsters with hereditary myocardiopathy and polymyopathy
3. Defective respiration and oxidative phosphorylation in muscle mitochondria of hamsters in the late stages of hereditary muscular dystrophy
4. Fatty acid metabolism in dystrophic muscle
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1. Is the fundamental pathology in Duchenne's muscular dystrophy caused by a failure of glycogenolysis–glycolysis in costameres?;Journal of Genetics;2023-01-09
2. Mitigation of pathological parameters under Jagged1 influence in DMD knockout zebrafish and patient-derived myoblast cultures;Indian Journal of Biochemistry and Biophysics;2023
3. Givinostat as metabolic enhancer reverting mitochondrial biogenesis deficit in Duchenne Muscular Dystrophy;Pharmacological Research;2021-08
4. Skeletal Muscle Mitochondria Dysfunction in Genetic Neuromuscular Disorders with Cardiac Phenotype;International Journal of Molecular Sciences;2021-07-08
5. Revisiting the dystrophin-ATP connection: How half a century of research still implicates mitochondrial dysfunction in Duchenne Muscular Dystrophy aetiology;Medical Hypotheses;2015-12
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