(Q24304454)

NADH:ubiquinone oxidoreductase core subunit S1

GOA release 2020-03-11

1 reference

NADH dehydrogenase (ubiquinone) activity

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

author

Massimo Zeviani

10

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Maria Ripoli

Maria Ripoli

8

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Vittoria Petruzzella

Vittoria Petruzzella

5

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Salvatore Scacco

Salvatore Scacco

2

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Sergio Papa

Sergio Papa

11

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Claudia Piccoli

3

Claudia Piccoli

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Francesco Bellomo

4

Francesco Bellomo

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Arcangela Iuso

1

Arcangela Iuso

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Nazzareno Capitanio

9

Nazzareno Capitanio

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Raffaella Trentadue

6

Raffaella Trentadue

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author name string

Michele Minuto

Journal of Biological Chemistry

7

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language of work or name

English

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publication date

14 April 2006

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published in

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volume

281

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issue

15

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page(s)

10374-80

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cites work

Human complex I deficiency: clinical spectrum and involvement of oxygen free radicals in the pathogenicity of the defect

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M513387200

Respiratory chain complex I deficiency: an underdiagnosed energy generation disorder

21 January 2018

1 reference

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Mutations in the complex I NDUFS2 gene of patients with cardiomyopathy and encephalomyopathy

21 January 2018

1 reference

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Mutations in human nuclear genes encoding for subunits of mitochondrial respiratory complex I: the NDUFS4 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M513387200

Clinical and molecular findings in children with complex I deficiency

21 January 2018

1 reference

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Mitochondrial complex I deficiency in Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M513387200

The reduction of NADH ubiquinone oxidoreductase 24- and 75-kDa subunits in brains of patients with Down syndrome and Alzheimer's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M513387200

Alzheimer's brains harbor somatic mtDNA control-region mutations that suppress mitochondrial transcription and replication

21 January 2018

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Complex I defect in muscle from patients with Huntington's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M513387200

Analysis of the subunit composition of complex I from bovine heart mitochondria

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M513387200

Familial myopathy: new insights into the T14709C mitochondrial tRNA mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M513387200

A nonsense mutation in the NDUFS4 gene encoding the 18 kDa (AQDQ) subunit of complex I abolishes assembly and activity of the complex in a patient with Leigh-like syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M513387200

Mutant NDUFS3 subunit of mitochondrial complex I causes Leigh syndrome

21 January 2018

1 reference

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NDUFS6 mutations are a novel cause of lethal neonatal mitochondrial complex I deficiency

21 January 2018

1 reference

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cAMP-dependent phosphorylation of the nuclear encoded 18-kDa (IP) subunit of respiratory complex I and activation of the complex in serum-starved mouse fibroblast cultures

21 January 2018

1 reference

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Cyclic adenosine monophosphate-dependent phosphorylation of mammalian mitochondrial proteins: enzyme and substrate characterization and functional role.

21 January 2018

1 reference

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Contribution of the phosphorylable complex I in the growth phase-dependent respiration of C6 glioma cells in vitro

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M513387200

Mutation in the NDUFS4 gene of complex I abolishes cAMP-dependent activation of the complex in a child with fatal neurological syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M513387200

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.M513387200

Pathological mutations of the human NDUFS4 gene of the 18-kDa (AQDQ) subunit of complex I affect the expression of the protein and the assembly and function of the complex

21 January 2018

1 reference

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A perfect message: RNA surveillance and nonsense-mediated decay

21 January 2018

1 reference

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Mutations in the NDUFS4 gene of mitochondrial complex I alter stability of the splice variants

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M513387200

Large-scale deletion and point mutations of the nuclear NDUFV1 and NDUFS1 genes in mitochondrial complex I deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M513387200

A convenient one-step extraction of cellular ATP using boiling water for the luciferin-luciferase assay of ATP.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M513387200

Loss of m-AAA protease in mitochondria causes complex I deficiency and increased sensitivity to oxidative stress in hereditary spastic paraplegia

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M513387200

Mitochondrial free radical generation, oxidative stress, and aging

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M513387200

Oxidants, oxidative stress and the biology of ageing

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M513387200

Generation of superoxide-radical by the NADH:ubiquinone oxidoreductase of heart mitochondria

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M513387200

Identification and characterization of a common set of complex I assembly intermediates in mitochondria from patients with complex I deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M513387200

Reversible glutathionylation of complex I increases mitochondrial superoxide formation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M513387200

Combined enzymatic complex I and III deficiency associated with mutations in the nuclear encoded NDUFS4 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M513387200

7 January 2021

Genotyping microsatellite DNA markers at putative disease loci in inbred/multiplex families with respiratory chain complex I deficiency allows rapid identification of a novel nonsense mutation (IVS1nt -1) in the NDUFS4 gene in Leigh syndrome

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M513387200

7 January 2021

Enzymic method for quantitative determination of nanogram amounts of total and oxidized glutathione: applications to mammalian blood and other tissues

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M513387200

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.M513387200

7 January 2021

Assays of glutathione peroxidase

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M513387200

7 January 2021

Dihydrofluorescein diacetate is superior for detecting intracellular oxidants: comparison with 2',7'-dichlorodihydrofluorescein diacetate, 5(and 6)-carboxy-2',7'-dichlorodihydrofluorescein diacetate, and dihydrorhodamine 123

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M513387200

7 January 2021

Mitochondrial membrane potential in single living adult rat cardiac myocytes exposed to anoxia or metabolic inhibition

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M513387200

7 January 2021

Role of NADH shuttle system in glucose-induced activation of mitochondrial metabolism and insulin secretion

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M513387200

7 January 2021