Mitochondrial myopathy: tissue-specific expression of a defect in ubiquinol-cytochrome c reductase.

No abstract is available for this paper.

• Publication year

  1986

• Venue

  Clinica chimica acta; international journal of clinical chemistry

• Publication date

  1986-08-15

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1016/0009-8981(86)90289-5PMID 3021360
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Analyses of muscle proteins in a patient with a mitochondrial myopathy.

  1985cited by this paper
• Cytochrome c oxidase deficiency.

  1985cited by this paper
• Mitochondrial myopathies: deficiencies localized to complex I and complex III of the mitochondrial respiratory chain.

  1985cited by this paper
• Six unidentified reading frames of human mitochondrial DNA encode components of the respiratory-chain NADH dehydrogenase

  1985cited by this paper
• Mitochondrial myopathy with lactic acidosis and deficient activity of muscle succinate cytochrome-c-oxidoreductase

  1984cited by this paper
• Histiocytoid Cardiomyopathy of Infancy: Deficiency of Reducible Cytochrome b in Heart Mitochondria

  1984cited by this paper
• 31P NMR study of improvement in oxidative phosphorylation by vitamins K3 and C in a patient with a defect in electron transport at complex III in skeletal muscle.

  1984cited by this paper
• Lactic Acidosis and Mitochondrial Myopathy Associated with Deficiency of Several Components of Complex III of the Respiratory Chain

  1984cited by this paper
• Mitochondrial myopathies: defects in mitochondrial metabolism in human skeletal muscle.

  1983cited by this paper
• Deficiency in ubiquinone cytochrome c reductase in a patient with mitochondrial myopathy and lactic acidosis.

  1983cited by this paper
• Tissue‐specific genes code for polypeptide VIa of bovine liver and heart cytochrome c oxidase

  1982cited by this paper
• Arrangement of proteins in the mitochondrial inner membrane.

  1982cited by this paper
• Mitochondrial Transmission Genetics: Replication, Recombination, and Segregation of Mitochondrial DNA and Its Inheritance in Crosses

  1982cited by this paper
• Mitochondrial encephalomyopathies: biochemical studies in two cases revealing defects in the respiratory chain.

  1982cited by this paper
• Cyclosporin A promotes spontaneous outgrowth in vitro of Epstein–Barr virus-induced B-cell lines

  1981cited by this paper
• Sequence and organization of the human mitochondrial genome

  1981cited by this paper
• Demonstration of a specific mitochondrial isovaleryl-CoA dehydrogenase deficiency in fibroblasts from patients with isovaleric acidemia.

  1980cited by this paper
• Fatal infantile mitochondrial myopathy and renal dysfunction due to cytochrome-c-oxidase deficiency.

  1980cited by this paper
• Biogenesis of mitochondrial proteins in HeLa cells.

  1979cited by this paper
• A mitochondrial myopathy characterized by a deficiency in reducible cytochrome b.

  1977cited by this paper
• Ultrastructural changes accompanying the aging of human diploid cells in culture.

  1972cited by this paper

• Mitochondrial encephalomyopathies and cytochrome c oxidase deficiency: muscle culture study

  2004cites this paper
• Antibody-based approaches to diagnosis and characterization of oxidative phosphorylation diseases.

  2001cites this paper
• Mitochondrial encephalomyopathy and complex III deficiency associated with a stop-codon mutation in the cytochrome b gene.

  2000cites this paper
• Utility of multimodal evoked potential study and electroencephalography in mitochondrial encephalomyopathy

  1998cites this paper
• Clinical heterogeneity in respiratory chain complex III deficiency in childhood.

  1997cites this paper
• Cytochrome c oxidase deficiency in fibroblasts of a patient with mitochondrial encephalomyopathy.

  1996cites this paper
• Metabolic myopathies.

  1996cites this paper
• Mitochondrial Myopathies: Biochemical Aspects

  1994cites this paper
• Deficiency of complex III of the mitochondrial respiratory chain in a patient with facioscapulohumeral disease.

  1991cites this paper
• 8 Defects of the respiratory chain

  1990cites this paper
• Cytochrome oxidase deficiency affecting the structure of the myofibre and the shape of mitochondrial cristae membrane.

  1990cites this paper
• Environmentally induced differential amplification of mitochondrial populations.

  1990cites this paper
• Defects of the respiratory chain.

  1990cites this paper
• Disorders of Pyruvate Metabolism, the Citric Acid Cycle, and the Respiratory Chain

  1990cites this paper
• Tissue specificity in cytochrome c oxidase deficient myopathy.

  1989cites this paper
• Myoclonus epilepsy and ragged-red fibres (MERRF). 1. A clinical, pathological, biochemical, magnetic resonance spectrographic and positron emission tomographic study.

  1989cites this paper
• Defects in the cytochromebc1 complex in mitochondrial diseases

  1988cites this paper
• Mitochondrial myopathies and respiratory chain proteins.

  1988cites this paper
• Mitochondrial myopathy involving ubiquinol-cytochrome c oxidoreductase (complex III) identified by immunoelectron microscopy.

  1987cites this paper
• Progressive dystonia with bilateral putaminal hypodensities.

  1987cites this paper
• The molecular aetiology of human mitochondrial myopathies.

  1987cites this paper
• Mitochondrial myopathies

  1987cites this paper