(Q24290607)

NADH:ubiquinone oxidoreductase core subunit S8

1 reference

NADH:ubiquinone oxidoreductase core subunit V1

1 reference

NADH:ubiquinone oxidoreductase subunit S4

1 reference

NADH:ubiquinone oxidoreductase subunit S5

1 reference

NADH:ubiquinone oxidoreductase core subunit S3

1 reference

NADH:ubiquinone oxidoreductase core subunit S7

1 reference

NADH:ubiquinone oxidoreductase core subunit S2

1 reference

NADH dehydrogenase activity

1 reference

1 reference

1 reference

R H Triepels

1

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B J Hanson

2

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L P van den Heuvel

3

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L Sundell

4

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M F Marusich

5

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J A Smeitink

6

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R A Capaldi

Journal of Biological Chemistry

7

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language of work or name

English

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publication date

23 March 2001

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published in

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volume

276

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issue

12

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page(s)

8892-7

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cites work

Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009903200

Isolated complex I deficiency in children: clinical, biochemical and genetic aspects

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009903200

The NADH:ubiquinone oxidoreductase (complex I) of respiratory chains

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009903200

Structure of the respiratory NADH:ubiquinone oxidoreductase (complex I)

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009903200

NADH:ubiquinone oxidoreductase from bovine heart mitochondria: sequence of a novel 17.2-kDa subunit.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009903200

Human mitochondrial complex I in health and disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009903200

Identification of two nuclear genes (ATP11, ATP12) required for assembly of the yeast F1-ATPase

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009903200

Mutations of SURF-1 in Leigh disease associated with cytochrome c oxidase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009903200

Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009903200

Two novel mutations of SURF1 in Leigh syndrome with cytochrome c oxidase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009903200

Missense mutations in SURF1 associated with deficient cytochrome c oxidase assembly in Leigh syndrome patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009903200

Purification and molecular and enzymic properties of mitochondrial NADH dehydrogenase

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009903200

Estimation of NADH oxidation in human skeletal muscle mitochondria.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009903200

Characterization of the human complex I NDUFB7 and 17.2-kDa cDNAs and mutational analysis of 19 genes of the HP fraction in complex I-deficient-patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009903200

Whole mitochondrial genome amplification reveals basal level multiple deletions in mtDNA of patients with dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009903200

Structure, functioning, and assembly of the ATP synthase in cells from patients with the T8993G mitochondrial DNA mutation. Comparison with the enzyme in Rho(0) cells completely lacking mtdna

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009903200

Leigh syndrome associated with a mutation in the NDUFS7 (PSST) nuclear encoded subunit of complex I.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009903200

The first nuclear-encoded complex I mutation in a patient with Leigh syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009903200

Demonstration of a new pathogenic mutation in human complex I deficiency: a 5-bp duplication in the nuclear gene encoding the 18-kD (AQDQ) subunit

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009903200

Mutant NDUFV1 subunit of mitochondrial complex I causes leukodystrophy and myoclonic epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009903200

Efficient hybridoma production using previously frozen splenocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009903200

7 January 2021

Mammalian cytochrome-c oxidase: characterization of enzyme and immunological detection of subunits in tissue extracts and whole cells

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009903200

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009903200

7 January 2021

Resolution of complex I and isolation of NADH dehydrogenase and an iron--sulfur protein

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009903200

7 January 2021

Expression of mtDNA and nDNA encoded respiratory chain proteins in chemically and genetically-derived Rho0 human fibroblasts: a comparison of subunit proteins in normal fibroblasts treated with ethidium bromide and fibroblasts from a patient with mt

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009903200

7 January 2021

Biochemical, genetic and immunoblot analyses of 17 patients with an isolated cytochrome c oxidase deficiency

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009903200

7 January 2021

Nuclear genes of human complex I of the mitochondrial electron transport chain: state of the art

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009903200

7 January 2021