Mitochondrial biogenesis dysfunction and metabolic dysfunction from a novel mitochondrial tRNAMet 4467 C>A mutation in a Han Chinese family with maternally inherited hypertension.

A Mitochondrial DNA A8701G Mutation Partly Associated with Maternally Inherited Hypertension and Dilated Cardiomyopathy in a Chinese Pedigree.

Systematic analysis of the clinical and biochemical characteristics of maternally inherited hypertension in Chinese Han families associated with mitochondrial.

A Mitochondrial DNA A8701G Mutation Associated with Maternally Inherited Hypertension and Dilated Cardiomyopathy in a Chinese Pedigree of a Consanguineous Marriage.

Mitochondrial mutations in maternally inherited hearing loss.

Maternally inherited myopathy and cardiomyopathy: association with mutation in mitochondrial DNA tRNA(Leu)(UUR).

Mitochondrial dysfunction in inherited renal disease and acute kidney injury.

Heterogeneous phenotypic manifestations of maternally inherited deafness associated with the mitochondrial A3243G mutation. Case report.

Mitochondrial respiratory dysfunction caused by a heteroplasmic mitochondrial DNA mutation blocks cellular reprogramming.

Mitochondrial injury and dysfunction in hypertension-induced cardiac damage.

Mitochondrial dysfunction in gliomas.

Amphetamines promote mitochondrial dysfunction and DNA damage in pulmonary hypertension.

Lipophilic antioxidants prevent lipopolysaccharide-induced mitochondrial dysfunction through mitochondrial biogenesis improvement.

Mitochondrial dysfunction in cancer.

A novel maternally inherited 8q24.3 and a rare paternally inherited 14q23.3 CNVs in a family with neurodevelopmental disorders.

Mitochondrial Dysfunction in Depression.

Mitochondrial dysfunction in cancer.

Novel CLCN7 mutation identified in a Han Chinese family with autosomal dominant osteopetrosis-2.

A novel point mutation in the mitochondrial tRNA(Leu)(UUR) gene in a family with mitochondrial myopathy.

Mitochondrial Dysfunction Meets Senescence.

Mitochondrial dysfunction and complications associated with diabetes.

The mitochondrial tRNA(Gln) T4353C mutation may not be associated with essential hypertension in Han Chinese population.

Exercise Intolerance and Myoglobinuria Associated with a Novel Maternally Inherited MT-ND1 Mutation.

Mitochondrial dysfunction and bipolar disorder.

Dysferlin mutations and mitochondrial dysfunction.

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A Mitochondrial DNA A8701G Mutation Partly Associated with Maternally Inherited Hypertension and Dilated Cardiomyopathy in a Chinese Pedigree.

Systematic analysis of the clinical and biochemical characteristics of maternally inherited hypertension in Chinese Han families associated with mitochondrial.

A Mitochondrial DNA A8701G Mutation Associated with Maternally Inherited Hypertension and Dilated Cardiomyopathy in a Chinese Pedigree of a Consanguineous Marriage.

Mitochondrial mutations in maternally inherited hearing loss.

Maternally inherited myopathy and cardiomyopathy: association with mutation in mitochondrial DNA tRNA(Leu)(UUR).

Mitochondrial dysfunction in inherited renal disease and acute kidney injury.

Heterogeneous phenotypic manifestations of maternally inherited deafness associated with the mitochondrial A3243G mutation. Case report.

Mitochondrial respiratory dysfunction caused by a heteroplasmic mitochondrial DNA mutation blocks cellular reprogramming.

Mitochondrial injury and dysfunction in hypertension-induced cardiac damage.

Mitochondrial dysfunction in gliomas.

Amphetamines promote mitochondrial dysfunction and DNA damage in pulmonary hypertension.

Lipophilic antioxidants prevent lipopolysaccharide-induced mitochondrial dysfunction through mitochondrial biogenesis improvement.

Mitochondrial dysfunction in cancer.

A novel maternally inherited 8q24.3 and a rare paternally inherited 14q23.3 CNVs in a family with neurodevelopmental disorders.

Mitochondrial Dysfunction in Depression.

Mitochondrial dysfunction in cancer.

Novel CLCN7 mutation identified in a Han Chinese family with autosomal dominant osteopetrosis-2.

A novel point mutation in the mitochondrial tRNA(Leu)(UUR) gene in a family with mitochondrial myopathy.

Mitochondrial Dysfunction Meets Senescence.

Mitochondrial dysfunction and complications associated with diabetes.

The mitochondrial tRNA(Gln) T4353C mutation may not be associated with essential hypertension in Han Chinese population.

Exercise Intolerance and Myoglobinuria Associated with a Novel Maternally Inherited MT-ND1 Mutation.

Mitochondrial dysfunction and bipolar disorder.

Dysferlin mutations and mitochondrial dysfunction.

Mitochondrial biogenesis dysfunction and metabolic dysfunction from a novel mitochondrial tRNAMet 4467 C>A mutation in a Han Chinese family with maternally inherited hypertension.

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