Genotype in the 24-kDa subunit gene (NDUFV2) of mitochondrial complex I and susceptibility to Parkinson disease (Q24312172)

NADH dehydrogenase (ubiquinone) activity

GOA release 2020-03-11

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GOA release 2020-03-11

author name string

N Hattori

1

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H Yoshino

2

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M Tanaka

3

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H Suzuki

4

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Y Mizuno

Variant cytochrome P450 CYP2D6 allelic frequencies in Parkinson's disease

5

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language of work or name

English

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publication date

1 April 1998

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published in

Genomics

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volume

49

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issue

1

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page(s)

52-8

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cites work

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Criteria for diagnosing Parkinson's disease

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Association of a monoamine oxidase B allele with Parkinson's disease

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An immunohistochemical study on alpha-ketoglutarate dehydrogenase complex in Parkinson's disease.

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An allelic association study of monoamine oxidase B in Parkinson's disease

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Hereditary variations in monoamine oxidase as a risk factor for Parkinson's disease

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Structural organization and chromosomal localization of the human nuclear gene (NDUFV2) for the 24-kDa iron-sulfur subunit of complex I in mitochondrial respiratory chain

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Structural dimorphism in the mitochondrial targeting sequence in the human manganese superoxide dismutase gene. A predictive evidence for conformational change to influence mitochondrial transport and a study of allelic association in Parkinson's di

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Mitochondrial DNA variants observed in Alzheimer disease and Parkinson disease patients.

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Deficiencies in complex I subunits of the respiratory chain in Parkinson's disease

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Neuromelanin-containing neurons of the substantia nigra accumulate iron and aluminum in Parkinson's disease: a LAMMA study

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Cloning and sequencing of a cDNA encoding the precursor to the 24 kDa iron-sulfur protein of human mitochondrial NADH dehydrogenase

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A simple method for displaying the hydropathic character of a protein

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Sequences of 20 subunits of NADH: Ubiquinone oxidoreductase from bovine heart mitochondria

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Sequences of 20 subunits of NADH:ubiquinone oxidoreductase from bovine heart mitochondria. Application of a novel strategy for sequencing proteins using the polymerase chain reaction

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Oxygen toxicity protecting enzymes in Parkinson's disease. Increase of superoxide dismutase-like activity in the substantia nigra and basal nucleus

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Mutant debrisoquine hydroxylation genes in Parkinson's disease

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Debrisoquine hydroxylase gene polymorphism and susceptibility to Parkinson's disease

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Point mutations of mitochondrial genome in Parkinson's disease.

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Molecular cloning and characterization of the active human mitochondrial NADH:ubiquinone oxidoreductase 24-kDa gene (NDUFV2) and its pseudogene

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Role of mitochondria in the etiology and pathogenesis of Parkinson's disease

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Is there a genetic susceptibility to idiopathic parkinsonism?

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The amino acid sequence of the 24-kDa subunit, an iron-sulfur protein, of rat liver mitochondrial NADH dehydrogenase deduced from cDNA sequence

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Aetiology of Parkinson's disease

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Mitochondrial complex I deficiency in Parkinson's disease

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Geography, drinking water chemistry, pesticides and herbicides and the etiology of Parkinson's disease

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Relationship between mitochondrial NADH-ubiquinone reductase and a bacterial NAD-reducing hydrogenase

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Mitochondrial NADH-ubiquinone reductase: complementary DNA sequences of import precursors of the bovine and human 24-kDa subunit

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Prediction of protein conformation

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Immunohistochemical detection of 4-hydroxynonenal protein adducts in Parkinson disease

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A simple salting out procedure for extracting DNA from human nucleated cells

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A novel cytochrome P-450IID6 mutant gene associated with Parkinson's disease

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Domain structure of mitochondrial and chloroplast targeting peptides

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Basal lipid peroxidation in substantia nigra is increased in Parkinson's disease

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Transition Metals, Ferritin, Glutathione, and Ascorbic Acid in Parkinsonian Brains

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A selective increase in particulate superoxide dismutase activity in parkinsonian substantia nigra

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Anatomic and disease specificity of NADH CoQ1 reductase (complex I) deficiency in Parkinson's disease

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Decreased ferritin levels in brain in Parkinson's disease

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Iron-melanin complex in substantia nigra of parkinsonian brains: an x-ray microanalysis

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Amino acid difference formula to help explain protein evolution

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New insights into the cause of Parkinson's disease

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