Muscle coenzyme Q deficiency in familial mitochondrial encephalomyopathy (Q28360128)

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A case of severe hypermetabolism of nonthyroid origin with a defect in the maintenance of mitochondrial respiratory control: a correlated clinical, biochemical, and morphological study

20 March 2017

1 reference

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Improvement of abnormal pyruvate metabolism and cardiac conduction defect with coenzyme Q10 in Kearns-Sayre syndrome

20 March 2017

1 reference

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Identification of 3-methoxy-4-hydroxy-5-hexaprenylbenzoic acid as a new intermediate in ubiquinone biosynthesis by Saccharomyces cerevisiae

20 March 2017

1 reference

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Protonmotive redox mechanism of the cytochrome b-c 1 complex in the respiratory chain: Protonmotive ubiquinone cycle

20 March 2017

1 reference

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New concepts on the role of ubiquinone in the mitochondrial respiratory chain

20 March 2017

1 reference

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Deficiency of the iron-sulfur clusters of mitochondrial reduced nicotinamide-adenine dinucleotide-ubiquinone oxidoreductase (complex I) in an infant with congenital lactic acidosis

29 September 2017

1 reference

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Arrangement of proteins in the mitochondrial inner membrane

29 September 2017

1 reference

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The mitochondrial electron transport and oxidative phosphorylation system

29 September 2017

1 reference

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The protonmotive Q cycle: A general formulation

29 September 2017

1 reference

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58 Isolation and characterization of intermediates in ubiquinone biosynthesis

29 September 2017

1 reference

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7 Preparation and properties of dihydroubiquinone: Cytochrome c oxidoreductase (complex III)

29 September 2017

1 reference

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Neuromuscular Disorder Associated With a Defect in Mitochondrial Energy Supply

29 September 2017

1 reference

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Studies on reduced and oxidized coenzyme Q (ubiquinones). II. The determination of oxidation-reduction levels of coenzyme Q in mitochondria, microsomes and plasma by high-performance liquid chromatography

29 September 2017

1 reference

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Identification of 3,4-dihydroxy-5-hexaprenylbenzoic acid as an intermediate in the biosynthesis of ubiquinone-6 by Saccharomyces cerevisiae

2 June 2018

1 reference

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Lactic Acidosis and Mitochondrial Myopathy Associated with Deficiency of Several Components of Complex III of the Respiratory Chain

2 June 2018

1 reference

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Biochemical studies of skeletal muscle mitochondria. I. Microanalysis of cytochrome content, oxidative and phosphorylative activities of mammalian skeletal muscle mitochondria

2 June 2018

1 reference

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Measurement of cytochromes in human skeletal muscle mitochondria, isolated from fresh and frozen stored muscle specimens

2 June 2018

1 reference

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A mitochondrial myopathy characterized by a deficiency in reducible cytochrome b.

2 June 2018

1 reference

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Respiratory enzymes in oxidative phosphorylation. I. Kinetics of oxygen utilization

2 June 2018

1 reference

https://pubmed.ncbi.nlm.nih.gov/2928337

12 December 2020

Hereditary mitochondrial myopathy with lactic acidemia, a De Toni-Fanconi-Debré syndrome, and a defective respiratory chain in voluntary striated muscles

1 reference

https://pubmed.ncbi.nlm.nih.gov/2928337

12 December 2020

Preparation and properties of NADH: ubiquinone oxidoreductase (complexI), EC 1.6.5.3

1 reference

https://pubmed.ncbi.nlm.nih.gov/2928337

12 December 2020

A mitochondrial myopathy with a deficiency of respiratory chain NADH-CoQ reductase activity

1 reference

https://pubmed.ncbi.nlm.nih.gov/2928337

12 December 2020

Liposome-mitochondrial inner membrane fusion. Lateral diffusion of integral electron transfer components

1 reference

https://pubmed.ncbi.nlm.nih.gov/2928337

12 December 2020

Benign infantile mitochondrial myopathy due to reversible cytochrome c oxidase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/2928337

12 December 2020

Mitochondrial myopathies: disorders of the respiratory chain and oxidative phosphorylation

1 reference

https://pubmed.ncbi.nlm.nih.gov/2928337

12 December 2020

Mitochondrial myopathies

1 reference

https://pubmed.ncbi.nlm.nih.gov/2928337

12 December 2020

Decreased activities in mitochondrial inner membrane electron transport system in muscle from patients with Kearns-Sayre syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2928337

12 December 2020