Mitochondrial DNA Depletion in Respiratory Chain-Deficient Parkinson Disease Neurons. - Wikidata - awgldk - TriplyDB

Mitochondrial DNA Depletion in Respiratory Chain-Deficient Parkinson Disease Neurons.

Mitochondrial DNA Depletion in Respiratory Chain-Deficient Parkinson Disease Neurons.

http://www.wikidata.org/entity/Q35852144

about

Mitochondrial DNA and primary mitochondrial dysfunction in Parkinson's disease.Colonic Oxidative and Mitochondrial Function in Parkinson's Disease and Idiopathic REM Sleep Behavior Disorder.Effect of high fat diet on phenotype, brain transcriptome and lipidome in Alzheimer's model mice Proteomic Analysis of the Effect of Korean Red Ginseng in the Striatum of a Parkinson's Disease Mouse Model.Mitochondrial dysfunction in myofibrillar myopathy.Lack of Parkin anticipates the phenotype and affects mitochondrial morphology and mtDNA levels in a mouse model of Parkinson's Disease.Neuronal complex I deficiency occurs throughout the Parkinson's disease brain, but is not associated with neurodegeneration or mitochondrial DNA damage.DGUOK recessive mutations in patients with CPEO, mitochondrial myopathy, parkinsonism and mtDNA deletions.Mitochondrial DNA changes in pedunculopontine cholinergic neurons in Parkinson disease.mtDNA Heteroplasmy in Monozygotic Twins Discordant for Schizophrenia.Single Cell Neurometabolomics.Mitochondrial DNA damage and reactive oxygen species in neurodegenerative disease.The mitochondrial transcription factor TFAM in neurodegeneration: emerging evidence and mechanisms.Sarcopenia, age, atrophy, and myopathy: Mitochondrial oxidative enzyme activities.Increased Degradation Rates in the Components of the Mitochondrial Oxidative Phosphorylation Chain in the Cerebellum of Old Mice.Mitochondrial Dysfunction in Parkinson's Disease: New Mechanistic Insights and Therapeutic Perspectives.Current perspective of mitochondrial biology in Parkinson's disease.Environmental and Genetic Variables Influencing Mitochondrial Health and Parkinson's Disease Penetrance.Cellular and Molecular Basis of Neurodegeneration in Parkinson Disease.Hallmarks of Brain Aging: Adaptive and Pathological Modification by Metabolic States.Reversing wrinkled skin and hair loss in mice by restoring mitochondrial function Droplet digital PCR shows the D-Loop to be an error prone locus for mitochondrial DNA copy number determination Subcellular origin of mitochondrial DNA deletions in human skeletal muscle

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P2860

Mitochondrial DNA Depletion in Respiratory Chain-Deficient Parkinson Disease Neurons.

http://www.wikidata.org/entity/Q35852144

description

2015 nî lūn-bûn

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2015年の論文

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2015年論文

@yue

2015年論文

@zh-hant

2015年論文

@zh-hk

2015年論文

@zh-mo

2015年論文

@zh-tw

2015年论文

@wuu

2015年论文

@zh

2015年论文

@zh-cn

name

Mitochondrial DNA Depletion in Respiratory Chain-Deficient Parkinson Disease Neurons.

@ast

Mitochondrial DNA Depletion in Respiratory Chain-Deficient Parkinson Disease Neurons.

@en

type

label

Mitochondrial DNA Depletion in Respiratory Chain-Deficient Parkinson Disease Neurons.

@ast

Mitochondrial DNA Depletion in Respiratory Chain-Deficient Parkinson Disease Neurons.

@en

prefLabel

Mitochondrial DNA Depletion in Respiratory Chain-Deficient Parkinson Disease Neurons.

@ast

Mitochondrial DNA Depletion in Respiratory Chain-Deficient Parkinson Disease Neurons.

@en

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P1433

Annals of Neurology

P1476

Mitochondrial DNA Depletion in Respiratory Chain-Deficient Parkinson Disease Neurons

@en

P2093

Anne Grünewald

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

Karolina A Rygiel

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

Philippa D Hepplewhite

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

P2860

Chronic Parkinsonism in humans due to a product of meperidine-analog synthesis

Control of mitochondrial transcription specificity factors (TFB1M and TFB2M) by nuclear respiratory factors (NRF-1 and NRF-2) and PGC-1 family coactivators

Relative abundance of the human mitochondrial transcription system and distinct roles for h-mtTFB1 and h-mtTFB2 in mitochondrial biogenesis and gene expression

Structure of human mitochondrial RNA polymerase

Distinct structural features of TFAM drive mitochondrial DNA packaging versus transcriptional activation

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

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

Quantitative quadruple-label immunofluorescence of mitochondrial and cytoplasmic proteins in single neurons from human midbrain tissue.

The ratio of oxidative phosphorylation complexes I-V in bovine heart mitochondria and the composition of respiratory chain supercomplexes.

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366-378

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scholarly article

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10.1002/ANA.24571

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3

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79

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Christopher M Morris

Doug M Turnbull

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2016-01-28T00:00:00Z

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284720597

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26605748

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Parkinson's disease

mitochondrial DNA

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4819690

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