Mitochondrial defects of brain and muscle.

Defects in mitochondrial DNA replication and oxidative damage in muscle of mtDNA mutator mice.

Mitochondrial myopathies: clinical defects.

Defects of mitochondrial DNA replication.

Mitochondrial dysfunction and defects in lipid homeostasis as therapeutic targets in neurodegeneration with brain iron accumulation.

Mitochondrial encephalomyopathies: defects of nuclear DNA.

Structural brain defects.

In vivo magnetic resonance spectroscopy of brain and muscle in a type of mitochondrial encephalomyopathy (MERRF).

Preservation of mitochondrial enzymes in brain and muscle in Reye's syndrome.

Reye's syndrome: preservation of mitochondrial enzymes in brain and muscle compared with liver.

CKD and Muscle Mitochondrial Energetics.

Mitochondrial Defects Confer Tolerance against Cellulose Deficiency.

Mitochondrial oxidative phosphorylation defects in Parkinson's disease.

Mitochondrial oxidative phosphorylation defects in Parkinson's disease.

Defects of fatty-acid oxidation in muscle.

Mouse mitochondrial lipid composition is defined by age in brain and muscle.

Brain, skeletal muscle and platelet homogenate mitochondrial function in Parkinson's disease.

Mitochondrial one-carbon metabolism and neural tube defects.

Mitochondrial respiratory defects promote the Warburg effect and cancer progression.

Polyglutamine toxicity in yeast induces metabolic alterations and mitochondrial defects.

Skeletal muscle mitochondrial energetic efficiency and aging.

Mitochondrial calcium and postmortem muscle shortening.

Specificity of expression of the muscle and brain dystrophin gene promoters in muscle and brain cells.

Mitochondrial Quality Control and Muscle Mass Maintenance.

Effect of triiodothyronine and thyroxine on mitochondrial alpha-glycerophosphate dehydrogenase activity and mitochondrial protein content of liver, muscle and brain of toad, Bufo melanostictus.

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Defects in mitochondrial DNA replication and oxidative damage in muscle of mtDNA mutator mice.

Mitochondrial myopathies: clinical defects.

Defects of mitochondrial DNA replication.

Mitochondrial dysfunction and defects in lipid homeostasis as therapeutic targets in neurodegeneration with brain iron accumulation.

Mitochondrial encephalomyopathies: defects of nuclear DNA.

Structural brain defects.

In vivo magnetic resonance spectroscopy of brain and muscle in a type of mitochondrial encephalomyopathy (MERRF).

Preservation of mitochondrial enzymes in brain and muscle in Reye's syndrome.

Reye's syndrome: preservation of mitochondrial enzymes in brain and muscle compared with liver.

CKD and Muscle Mitochondrial Energetics.

Mitochondrial Defects Confer Tolerance against Cellulose Deficiency.

Mitochondrial oxidative phosphorylation defects in Parkinson's disease.

Mitochondrial oxidative phosphorylation defects in Parkinson's disease.

Defects of fatty-acid oxidation in muscle.

Mouse mitochondrial lipid composition is defined by age in brain and muscle.

Brain, skeletal muscle and platelet homogenate mitochondrial function in Parkinson's disease.

Mitochondrial one-carbon metabolism and neural tube defects.

Mitochondrial respiratory defects promote the Warburg effect and cancer progression.

Polyglutamine toxicity in yeast induces metabolic alterations and mitochondrial defects.

Skeletal muscle mitochondrial energetic efficiency and aging.

Mitochondrial calcium and postmortem muscle shortening.

Specificity of expression of the muscle and brain dystrophin gene promoters in muscle and brain cells.

Mitochondrial Quality Control and Muscle Mass Maintenance.

Effect of triiodothyronine and thyroxine on mitochondrial alpha-glycerophosphate dehydrogenase activity and mitochondrial protein content of liver, muscle and brain of toad, Bufo melanostictus.

Mitochondrial defects of brain and muscle.

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