Dissecting the mechanisms underlying the accumulation of mitochondrial DNA deletions in human skeletal muscle

Keyphrases

• Human Skeletal muscle 100%
• Mitochondrial DNA mutation 100%
• Clonal Expansion 33%
• Muscle Fiber 25%
• Mitochondrial DNA 16%
• Mitochondrial DNA Maintenance 16%
• Maintenance Disorders 16%
• No Significant Difference 8%
• Neurodegenerative Diseases 8%
• Large Mode Area Fiber 8%
• Mitochondrial Disease 8%
• Oxidase 8%
• Human muscle 8%
• Cytochrome c Oxidase 8%
• Small Fibers 8%
• Respiratory Chain Deficiency 8%
• Cellular Pathology 8%
• MtDNA Heteroplasmy 8%
• Age-related Illnesses 8%

Biochemistry, Genetics and Molecular Biology

• Skeletal Muscle 100%
• Mitochondrial DNA 100%
• Mitochondrial Genome 13%
• Oxidase 6%
• Heteroplasmy 6%
• Electron Transport Chain 6%
• Mitochondrial Disease 6%
• Oxidoreductase 6%
• Cytochrome C Oxidase 6%