Somatic mitochondrial DNA mutations in early Parkinson and incidental Lewy body disease. - Wikidata - awgldk - TriplyDB

Somatic mitochondrial DNA mutations in early Parkinson and incidental Lewy body disease.

Somatic mitochondrial DNA mutations in early Parkinson and incidental Lewy body disease.

http://www.wikidata.org/entity/Q34311330

about

Combined defects in oxidative phosphorylation and fatty acid β-oxidation in mitochondrial disease Dysregulation of autophagy and mitochondrial function in Parkinson's disease Mitochondrial Biology and Neurological Diseases Mitochondrial defects and oxidative stress in Alzheimer disease and Parkinson disease Somatic alpha-synuclein mutations in Parkinson's disease: hypothesis and preliminary data.Mitochondrial DNA and primary mitochondrial dysfunction in Parkinson's disease.Mitochondria-Derived Damage-Associated Molecular Patterns in Neurodegeneration.Somatic mitochondrial DNA mutations do not increase neuronal vulnerability to MPTP in young POLG mutator mice.Ultra-sensitive sequencing reveals an age-related increase in somatic mitochondrial mutations that are inconsistent with oxidative damage Metabolomic analysis of exercise effects in the POLG mitochondrial DNA mutator mouse brain Behavioral and metabolic characterization of heterozygous and homozygous POLG mutator mice.The impact of mitochondrial DNA and nuclear genes related to mitochondrial functioning on the risk of Parkinson's disease.Mitochondrial DNA point mutations and relative copy number in 1363 disease and control human brains.Oxidative damage to macromolecules in human Parkinson disease and the rotenone model.The hallmarks of Parkinson's disease.The role of DNA base excision repair in brain homeostasis and disease.Molecular changes in the postmortem parkinsonian brain.Amelioration of premature aging in mtDNA mutator mouse by exercise: the interplay of oxidative stress, PGC-1α, p53, and DNA damage. A hypothesis.Calcium: Alpha-Synuclein Interactions in Alpha-Synucleinopathies.Mitochondrial DNA mutations increase in early stage Alzheimer disease and are inconsistent with oxidative damage.Mitochondrial DNA mutations in Parkinson's disease brain.Response to Simon et al.iPS cells in the study of PD molecular pathogenesis.Capture of somatic mtDNA point mutations with severe effects on oxidative phosphorylation in synaptosome cybrid clones from human brain.Mitochondrial DNA damage and reactive oxygen species in neurodegenerative disease.The mitochondrial transcription factor TFAM in neurodegeneration: emerging evidence and mechanisms.Is There Still Any Role for Oxidative Stress in Mitochondrial DNA-Dependent Aging?Current perspective of mitochondrial biology in Parkinson's disease.Mitochondrial Dysfunction in Parkinson's Disease.HSP90-incorporating chaperome networks as biosensor for disease-related pathways in patient-specific midbrain dopamine neurons

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Somatic mitochondrial DNA mutations in early Parkinson and incidental Lewy body disease.

http://www.wikidata.org/entity/Q34311330

description

2012 nî lūn-bûn

@nan

2012 թուականի Յունիսին հրատարակուած գիտական յօդուած

@hyw

2012 թվականի հունիսին հրատարակված գիտական հոդված

@hy

2012年の論文

@ja

2012年論文

@yue

2012年論文

@zh-hant

2012年論文

@zh-hk

2012年論文

@zh-mo

2012年論文

@zh-tw

2012年论文

@wuu

name

Somatic mitochondrial DNA mutations in early Parkinson and incidental Lewy body disease.

@ast

Somatic mitochondrial DNA mutations in early Parkinson and incidental Lewy body disease.

@en

Somatic mitochondrial DNA mutations in early Parkinson and incidental Lewy body disease.

@nl

type

label

Somatic mitochondrial DNA mutations in early Parkinson and incidental Lewy body disease.

@ast

Somatic mitochondrial DNA mutations in early Parkinson and incidental Lewy body disease.

@en

Somatic mitochondrial DNA mutations in early Parkinson and incidental Lewy body disease.

@nl

prefLabel

Somatic mitochondrial DNA mutations in early Parkinson and incidental Lewy body disease.

@ast

Somatic mitochondrial DNA mutations in early Parkinson and incidental Lewy body disease.

@en

Somatic mitochondrial DNA mutations in early Parkinson and incidental Lewy body disease.

@nl

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P1433

Annals of Neurology

P1476

Somatic mitochondrial DNA mutations in early Parkinson and incidental Lewy body disease.

@en

P2093

David K Simon

http://www.w3.org/2001/XMLSchema#string

Ippolita Cantuti-Castelvetri

http://www.w3.org/2001/XMLSchema#string

Kangni Zheng

http://www.w3.org/2001/XMLSchema#string

Katie E Jackson

http://www.w3.org/2001/XMLSchema#string

M Flint Beal

http://www.w3.org/2001/XMLSchema#string

Michael T Lin

http://www.w3.org/2001/XMLSchema#string

Rebecca A Betensky

http://www.w3.org/2001/XMLSchema#string

Thomas Arzberger

http://www.w3.org/2001/XMLSchema#string

Yong B Tan

http://www.w3.org/2001/XMLSchema#string

P2860

Premature ageing in mice expressing defective mitochondrial DNA polymerase

Chronic systemic pesticide exposure reproduces features of Parkinson's disease

Stages in the development of Parkinson's disease-related pathology

Mitochondrial DNA mutations, oxidative stress, and apoptosis in mammalian aging

High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease

Mitochondrial ND5 mutations in idiopathic Parkinson's disease.

Parkinson's disease brain mitochondria have impaired respirasome assembly, age-related increases in distribution of oxidative damage to mtDNA and no differences in heteroplasmic mtDNA mutation abundance

Origin and functional consequences of the complex I defect in Parkinson's disease.

High aggregate burden of somatic mtDNA point mutations in aging and Alzheimer's disease brain.

Mitochondria in the aetiology and pathogenesis of Parkinson's disease.

P304

850-854

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scholarly article

P356

10.1002/ANA.23568

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P433

6

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71

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Andrew John Lees

P577

2012-06-01T00:00:00Z

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P5875

227710430

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P698

22718549

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P921

Parkinson's disease

mitochondrial DNA

P932

3383820

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