(Q37630968)

21 August 2017

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title

Mitochondrial respiratory dysfunction and mutations in mitochondrial DNA in PINK1 familial parkinsonism (English)

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21 August 2017

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Sergio Papa

1

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21 August 2017

Anna Maria Sardanelli

series ordinal

2

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21 August 2017

Nazzareno Capitanio

series ordinal

3

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21 August 2017

Claudia Piccoli

series ordinal

4

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21 August 2017

publication date

1 December 2009

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Journal of Bioenergetics and Biomembranes

21 August 2017

published in

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21 August 2017

volume

41

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21 August 2017

issue

6

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21 August 2017

page(s)

509-516

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Redox imbalance in Parkinson's disease

21 August 2017

cites work

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Crossref

https://api.crossref.org/works/10.1007%2FS10863-009-9252-4

GRIM-19, a cell death regulatory gene product, is a subunit of bovine mitochondrial NADH:ubiquinone oxidoreductase (complex I)

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10863-009-9252-4

PINK1 controls mitochondrial localization of Parkin through direct phosphorylation

21 January 2018

1 reference

12 December 2020

Mitochondrial free radical generation, oxidative stress, and aging

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12 December 2020

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

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12 December 2020

Diphenyleneiodonium inhibits reduction of iron-sulfur clusters in the mitochondrial NADH-ubiquinone oxidoreductase (Complex I)

1 reference

12 December 2020

Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase

1 reference

12 December 2020

Leber hereditary optic neuropathy mutations in the ND6 subunit of mitochondrial complex I affect ubiquinone reduction kinetics in a bacterial model of the enzyme

1 reference

12 December 2020

Mitochondrial dysfunction, peroxidation damage and changes in glutathione metabolism in PARK6.

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12 December 2020

Early-onset parkinsonism associated with PINK1 mutations: frequency, genotypes, and phenotypes

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12 December 2020

The mitochondrial ND6 gene is a hot spot for mutations that cause Leber's hereditary optic neuropathy

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12 December 2020

Calpain 10: a mitochondrial calpain and its role in calcium-induced mitochondrial dysfunction

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12 December 2020

ROS-generating mitochondrial DNA mutations can regulate tumor cell metastasis

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12 December 2020

Familial Parkinson disease gene product, parkin, is a ubiquitin-protein ligase

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12 December 2020

Dysfunctions of cellular oxidative metabolism in patients with mutations in the NDUFS1 and NDUFS4 genes of complex I

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12 December 2020

Neurotoxicity of MAO metabolites of catecholamine neurotransmitters: role in neurodegenerative diseases

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12 December 2020

Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism

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12 December 2020

Mitochondrial import and enzymatic activity of PINK1 mutants associated to recessive parkinsonism.

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12 December 2020

Inhibition of growth and increase of alkaline phosphatase activity in cultured human oral cancer cells by all-trans retinoic acid

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12 December 2020

The phosphorylation pattern of bovine heart complex I subunits

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12 December 2020

Mitochondrial dysfunction and oxidative stress in neurodegenerative diseases

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12 December 2020

Inhibition of NADPH oxidase activation in endothelial cells by ortho-methoxy-substituted catechols

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12 December 2020

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

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12 December 2020

DJ-1 has a role in antioxidative stress to prevent cell death

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12 December 2020

Impaired mitochondrial dynamics and function in the pathogenesis of Parkinson's disease

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12 December 2020

Mitochondria in the aetiology and pathogenesis of Parkinson's disease

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12 December 2020

Mitochondrial respiratory dysfunction in familiar parkinsonism associated with PINK1 mutation.

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12 December 2020

PINK1 protects against oxidative stress by phosphorylating mitochondrial chaperone TRAP1

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12 December 2020

Protein phosphatase 2A associates with Rb2/p130 and mediates retinoic acid-induced growth suppression of ovarian carcinoma cells

1 reference

12 December 2020

Characterization of the membrane domain subunit NuoJ (ND6) of the NADH-quinone oxidoreductase from Escherichia coli by chromosomal DNA manipulation

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12 December 2020

Mutation in the alpha-synuclein gene identified in families with Parkinson's disease

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12 December 2020

Emerging pathways in genetic Parkinson's disease: autosomal-recessive genes in Parkinson's disease--a common pathway?

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12 December 2020

Differential effects of all-trans retinoic acid on the growth of human keratinocytes and mouth carcinoma epidermoid cultures. Involvement of GRIM-19 and complex I of the respiratory chain.

1 reference

12 December 2020

Analysis of the assembly profiles for mitochondrial- and nuclear-DNA-encoded subunits into complex I

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12 December 2020

Biochemical features of mtDNA 14484 (ND6/M64V) point mutation associated with Leber's hereditary optic neuropathy

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12 December 2020

Biochemical aspects of the neuroprotective mechanism of PTEN-induced kinase-1 (PINK1)

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12 December 2020

Hereditary early-onset Parkinson's disease caused by mutations in PINK1

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12 December 2020

PINK1 homozygous W437X mutation in a patient with apparent dominant transmission of parkinsonism

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12 December 2020

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12 December 2020

Identification of GRIM-19, a novel cell death-regulatory gene induced by the interferon-beta and retinoic acid combination, using a genetic approach

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12 December 2020

GRIM-19, a cell death regulatory protein, is essential for assembly and function of mitochondrial complex I

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12 December 2020

GRIM-19 associates with the serine protease HtrA2 for promoting cell death

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12 December 2020

Whole gene deletion and splicing mutations expand the PINK1 genotypic spectrum

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12 December 2020

Coexistence of mutations in PINK1 and mitochondrial DNA in early onset parkinsonism

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12 December 2020

The kinase domain of mitochondrial PINK1 faces the cytoplasm

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12 December 2020

cAMP response element-binding protein (CREB) is imported into mitochondria and promotes protein synthesis.

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12 December 2020

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

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12 December 2020

Mitochondrial localization of DJ-1 leads to enhanced neuroprotection

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12 December 2020

Parkin mitochondria in the autophagosome

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12 December 2020

Loss of function mutations in the gene encoding Omi/HtrA2 in Parkinson's disease

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12 December 2020

cAMP controls oxygen metabolism in mammalian cells

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12 December 2020

Mitochondrial biogenesis and mitochondrial DNA maintenance of mammalian cells under oxidative stress.

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12 December 2020

Pathogenetic mechanisms in hereditary dysfunctions of complex I of the respiratory chain in neurological diseases

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12 December 2020

The ubiquitin pathway in Parkinson's disease

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12 December 2020

Molecular Pathways of Neurodegeneration in Parkinson's Disease

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12 December 2020

Free radicals-mediated damage in transmitochondrial cells harboring the T14487C mutation in the ND6 gene of mtDNA

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12 December 2020

The genetics and pathology of oxidative phosphorylation

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12 December 2020

Energy converting NADH:quinone oxidoreductase (complex I).

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12 December 2020

Drosophila pink1 is required for mitochondrial function and interacts genetically with parkin

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12 December 2020

Parkin is recruited selectively to impaired mitochondria and promotes their autophagy

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12 December 2020

PINK1 mutants associated with recessive Parkinson's disease are defective in inhibiting mitochondrial release of cytochrome c.

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12 December 2020

Genetics of Parkinson disease: paradigm shifts and future prospects.

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12 December 2020

The mitochondrial protease HtrA2 is regulated by Parkinson's disease-associated kinase PINK1.

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12 December 2020

Expanding insights of mitochondrial dysfunction in Parkinson's disease.

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12 December 2020

Complex I deficiency in Parkinson's disease frontal cortex

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12 December 2020

Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology

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12 December 2020

Parkin, PINK1, and DJ-1 form a ubiquitin E3 ligase complex promoting unfolded protein degradation

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12 December 2020

Reactive oxygen species, mitochondria, apoptosis and aging.

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12 December 2020

How mitochondria produce reactive oxygen species

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12 December 2020

Pink1 regulates mitochondrial dynamics through interaction with the fission/fusion machinery

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12 December 2020

C-terminal truncation and Parkinson's disease-associated mutations down-regulate the protein serine/threonine kinase activity of PTEN-induced kinase-1.

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12 December 2020

Mitochondrial localization of the Parkinson's disease related protein DJ-1: implications for pathogenesis

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12 December 2020

Energy substrate modulates mitochondrial structure and oxidative capacity in cancer cells

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12 December 2020

cAMP-dependent protein kinase regulates the mitochondrial import of the nuclear encoded NDUFS4 subunit of complex I.

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12 December 2020

The Parkinson disease causing LRRK2 mutation I2020T is associated with increased kinase activity

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12 December 2020

Parkinson's disease brain mitochondrial complex I has oxidatively damaged subunits and is functionally impaired and misassembled.

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12 December 2020

10.1007/S10863-009-9252-4

Identifiers

DOI

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21 August 2017

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