(Q69834284)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2841308%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

title

Defects in the cytochrome bc1 complex in mitochondrial diseases (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2841308%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

author name string

N G Kennaway

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2841308%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

publication date

1 June 1988

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2841308%20AND%20SRC:MED&resulttype=core&format=json

Journal of Bioenergetics and Biomembranes

6 October 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2841308%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

volume

20

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2841308%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2841308%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

page(s)

325-352

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2841308%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/bf00769636

6 October 2019

exact match

0 references

cites work

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

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Sequence and organization of the human mitochondrial genome

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Cytochrome b is necessary for the effective processing of core protein I and the iron-sulfur protein of complex III in the mitochondria

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Purification of all thirteen polypeptides of bovine heart cytochrome c oxidase from one aliquot of enzyme. Characterization of bovine fetal heart cytochrome c oxidase

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Morphological observations in skeletal muscle from patients with a mitochondrial myopathy

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Treatment of mitochondrial myopathy due to complex III deficiency with vitamins K3 and C: A 31P-NMR follow-up study

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12 December 2020

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

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Fatal infantile cytochrome c oxidase deficiency: decrease of immunologically detectable enzyme in muscle

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12 December 2020

A mitochondrial myopathy with a defective respiratory chain and carnitine deficiency

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12 December 2020

Partial deficiency of subunits in complex I or IV of patients with mitochondrial myopathies

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12 December 2020

Difficulties in assessing biochemical properties of abnormal muscle mitochondria

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12 December 2020

Myoclonus epilepsy associated with ragged-red fibres (mitochondrial abnormalities ): disease entity or a syndrome? Light-and electron-microscopic studies of two cases and review of literature

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A mitochondrial encephalomyopathy: the first case with an established defect at the level of coenzyme Q.

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A novel mutation selectively decreases complex I and cytochrome c oxidase subunits in Chinese hamster mitochondria

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12 December 2020

Differential investigation of the capacity of succinate oxidation in human skeletal muscle

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Kearns-Sayre syndrome with reduced plasma and cerebrospinal fluid folate

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Multiple cytochrome deficiency and deteriorated mitochondrial polypeptide composition in fatal infantile mitochondrial myopathy and renal dysfunction

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12 December 2020

How are proteins imported into mitochondria?

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12 December 2020

Transcription of the mammalian mitochondrial genome

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12 December 2020

Fatal infhntile mitochondrial myopathy and renal dysfunction due to cytochrome-c-oxidase deficiency

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12 December 2020

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

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12 December 2020

Tissue-specific genes code for polypeptide VIa of bovine liver and heart cytochrome c oxidase

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12 December 2020

Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies

1 reference

12 December 2020

Chronic progressive external ophthalmoplegia (CPEO): Clinical, morphologic, and biochemical studies

1 reference

12 December 2020

An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytes

1 reference

12 December 2020

Cooperative Interaction between Mitochondrial and Nuclear Genomes: Cytochrome c Oxidase Assembly as a Model

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12 December 2020

Maternal inheritance of human mitochondrial DNA

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12 December 2020

Therapy of mitochondrial disorders

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12 December 2020

Mitochondria1 encephalomyopathy with decreased succinate-cytochrome c reductase activity

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12 December 2020

Pyruvate oxidation in rat and human skeletal muscle mitochondria

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12 December 2020

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

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12 December 2020

Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: A distinctive clinical syndrome

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12 December 2020

Deficiency in ubiquinone cytochrome c reductase in a patient with mitochondrial myopathy and lactic acidosis

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12 December 2020

A new mitochondrial myopathy. Biochemical studies revealing a deficiency in the cytochrome b-c1 complex (complex III) of the respiratory chain

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12 December 2020

Assembly of the mitochondrial membrane system. CBP6, a yeast nuclear gene necessary for synthesis of cytochrome b.

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Peroxisomal and mitochondrial defects in the cerebro-hepato-renal syndrome

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Maternally inherited mitochondrial myopathy and myoclonic epilepsy.

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12 December 2020

Mitochondrial myopathy due to complex III deficiency with normal reducible cytochrome b concentration

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Identification and cloning of a yeast nuclear gene (CBP1) involved in expression of mitochondrial cytochrome b.

1 reference

12 December 2020

Mitochondrial myopathy involving ubiquinol-cytochrome c oxidoreductase (complex III) identified by immunoelectron microscopy

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12 December 2020

Adenine nucleotide transport in sonic submitochondrial particles. Kinetic properties and binding of specific inhibitors

1 reference

12 December 2020

Subunit II of yeast QH2:cytochrome-c oxidoreductase. Nucleotide sequence of the gene and features of the protein

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12 December 2020

Deficiency of cytochromes b and aa3 in muscle from a floppy infant with cytochrome oxidase deficiency

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12 December 2020

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12 December 2020

Mitochondrial myopathies: deficiencies localized to complex I and complex III of the mitochondrial respiratory chain.

1 reference

12 December 2020

Mitochondrial myopathies

1 reference

12 December 2020

Isolation and properties of cytochrome c oxidase from rat liver and quantification of immunological differences between isozymes from various rat tissues with subunit-specific antisera

1 reference

12 December 2020

Lumping or splitting? "Ophthalmoplegia-plus" or Kearns-Sayre syndrome?

1 reference

12 December 2020

Mitochondrial myopathies involving the respiratory chain: a biochemical analysis

1 reference

12 December 2020

Mitochondrial genes and disease

1 reference

12 December 2020

Peroxisomal disorders: a newly recognised group of genetic diseases

1 reference

12 December 2020

Histiocytoid Cardiomyopathy of Infancy: Deficiency of Reducible Cytochrome b in Heart Mitochondria

1 reference

12 December 2020

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

1 reference

12 December 2020

Phosphorus magnetic resonance spectroscopy studies of the role of mitochondria in the disease process

1 reference

12 December 2020

Mitochondrial myopathies: defects in mitochondrial metabolism in human skeletal muscle.

1 reference

12 December 2020

Defects in citric acid cycle and the electron transport chain in progressive poliodystrophy.

1 reference

12 December 2020

An electron-transport system associated with the outer membrane of liver mitochondria. A biochemical and morphological study

1 reference

12 December 2020

The inborn errors of mitochondrial fatty acid oxidation

1 reference

12 December 2020

Defects in oxidative phosphorylation. Biochemical investigations in skeletal muscle and expression of the lesion in other cells

1 reference

12 December 2020