Pages that link to "Q69958309"
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The following pages link to Mitochondrial myopathies (Q69958309):
Displaying 50 items.
- Mitochondrial encephalomyopathy: variable clinical expression within a single kindred (Q24514945) (← links)
- Mitochondrial myopathy: a genetic study of 71 cases (Q24522304) (← links)
- Replication-competent human mitochondrial DNA lacking the heavy-strand promoter region (Q24607395) (← links)
- A mitochondrial DNA variant, identified in Leber hereditary optic neuropathy patients, which extends the amino acid sequence of cytochrome c oxidase subunit I (Q24670009) (← links)
- Formation of cristae and crista junctions in mitochondria depends on antagonism between Fcj1 and Su e/g. (Q27929830) (← links)
- MIP1, a new yeast gene homologous to the rat mitochondrial intermediate peptidase gene, is required for oxidative metabolism in Saccharomyces cerevisiae (Q27930008) (← links)
- Oxidative myocytes of heart and skeletal muscle express abundant sarcomeric mitochondrial creatine kinase (Q28142966) (← links)
- Myo-, neuro-, gastrointestinal encephalopathy (MNGIE syndrome) due to partial deficiency of cytochrome-c-oxidase. A new mitochondrial multisystem disorder (Q28280475) (← links)
- Effect of 'binary mitochondrial heteroplasmy' on respiration and ATP synthesis: implications for mitochondrial diseases (Q28344441) (← links)
- Muscle coenzyme Q deficiency in familial mitochondrial encephalomyopathy (Q28360128) (← links)
- Transgenic overexpression of mitofilin attenuates diabetes mellitus-associated cardiac and mitochondria dysfunction (Q28386173) (← links)
- Historical perspective on mitochondrial medicine (Q28661465) (← links)
- Muscle oxidative phosphorylation quantitation using creatine chemical exchange saturation transfer (CrCEST) MRI in mitochondrial disorders (Q28820743) (← links)
- Human cells lacking mtDNA: repopulation with exogenous mitochondria by complementation (Q29614475) (← links)
- The C-terminal domain of Fcj1 is required for formation of crista junctions and interacts with the TOB/SAM complex in mitochondria (Q30155339) (← links)
- The mitochondrial respiratory chain controls intracellular calcium signaling and NFAT activity essential for heart formation in Xenopus laevis (Q30480776) (← links)
- Epilepsy in a mitochondrial disorder (Q33590168) (← links)
- Screening for mitochondrial cytopathies: the sub-anaerobic threshold exercise test (SATET). (Q33627799) (← links)
- Biochemical studies in mitochondrial encephalomyopathy (Q33629607) (← links)
- Restriction endonuclease analysis of leukocyte mitochondrial DNA in Leber's optic atrophy (Q33631235) (← links)
- Restriction enzyme analysis of the mitochondrial genome in mitochondrial myopathy (Q33681824) (← links)
- MELAS syndrome with mitochondrial tRNA(Leu(UUR)) gene mutation in a Chinese family (Q33732462) (← links)
- Metabolic myopathies. A diagnostic evaluation (Q33829436) (← links)
- Myoclonus and epilepsies (Q33894847) (← links)
- Cardiomyopathy in the Kearns-Sayre syndrome (Q33999538) (← links)
- Clinical and molecular studies of mitochondrial disease (Q34280992) (← links)
- Exercise intolerance, lactic acidosis, and abnormal cardiopulmonary regulation in exercise associated with adult skeletal muscle cytochrome c oxidase deficiency (Q34450667) (← links)
- Neuromuscular manifestations of endocrine disorders (Q34469054) (← links)
- Chronic intestinal pseudoobstruction and ophthalmoplegia in a patient with mitochondrial myopathy (Q34529668) (← links)
- X-linked dilated cardiomyopathy with neutropenia, growth retardation, and 3-methylglutaconic aciduria (Q34595191) (← links)
- A new mitochondrial disease associated with mitochondrial DNA heteroplasmy (Q34627393) (← links)
- Iron-overload disease in infants involving fetal growth retardation, lactic acidosis, liver haemosiderosis, and aminoaciduria (Q34745515) (← links)
- A molecular basis for human hypersensitivity to aminoglycoside antibiotics (Q35000709) (← links)
- Respiration-deficient cells are caused by a single point mutation in the mitochondrial tRNA-Leu (UUR) gene in mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS) (Q35196821) (← links)
- Genetic heterogeneity in Leber hereditary optic neuroretinopathy revealed by mitochondrial DNA polymorphism (Q35197226) (← links)
- Mitochondrial creatine kinase: a major constituent of pathological inclusions seen in mitochondrial myopathies (Q35369919) (← links)
- Deficiency of the reduced nicotinamide adenine dinucleotide dehydrogenase component of complex I of mitochondrial electron transport. Fatal infantile lactic acidosis and hypermetabolism with skeletal-cardiac myopathy and encephalopathy (Q35575407) (← links)
- Cytoplasmic transfer of the mtDNA nt 8993 T-->G (ATP6) point mutation associated with Leigh syndrome into mtDNA-less cells demonstrates cosegregation with a decrease in state III respiration and ADP/O ratio (Q35696491) (← links)
- Cytochrome-c-oxidase deficient cardiomyocytes in the human heart--an age-related phenomenon. A histochemical ultracytochemical study. (Q35816863) (← links)
- Visualization of mitochondrial respiratory function using cytochrome c oxidase/succinate dehydrogenase (COX/SDH) double-labeling histochemistry (Q35841506) (← links)
- Deletions of the mitochondrial genome (Q35848675) (← links)
- Mitochondrial disorders in pediatrics. Clinical, biochemical, and genetic implications. (Q35942786) (← links)
- Mitochondrial encephalomyopathy with pilovacuolar inclusion or phenocopy with mitochondrial artefact? (Q36220580) (← links)
- Late onset familial dystonia: could mitochondrial deficits induce a diffuse lesioning process of the whole basal ganglia system? (Q36317027) (← links)
- Leigh syndrome, a mitochondrial encephalo(myo)pathy. A review of the literature (Q36447731) (← links)
- Quantitative nuclear magnetic resonance imaging: characterisation of experimental cerebral oedema (Q36465659) (← links)
- Contribution of somatic mutations in the mitochondrial genome to the development of cancer and tolerance against anticancer drugs (Q36558016) (← links)
- Neurological disease and mitochondrial genes (Q36654770) (← links)
- Adult-onset mitochondrial myopathy (Q36682510) (← links)
- In vitro genetic transfer of protein synthesis and respiration defects to mitochondrial DNA-less cells with myopathy-patient mitochondria (Q36689236) (← links)