Accumulation of mitochondrial DNA deletions within dopaminergic neurons triggers neuroprotective mechanisms.
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Ageing and Parkinson's disease: why is advancing age the biggest risk factor?Lack of GDAP1 induces neuronal calcium and mitochondrial defects in a knockout mouse model of charcot-marie-tooth neuropathyMitochondrial DNA and primary mitochondrial dysfunction in Parkinson's disease.Somatic mitochondrial DNA mutations do not increase neuronal vulnerability to MPTP in young POLG mutator mice.Mitochondrial alterations by PARKIN in dopaminergic neurons using PARK2 patient-specific and PARK2 knockout isogenic iPSC lines.Mitochondrial Diseases Part II: Mouse models of OXPHOS deficiencies caused by defects in regulatory factors and other components required for mitochondrial function.The Polg Mutator Phenotype Does Not Cause Dopaminergic Neurodegeneration in DJ-1-Deficient Mice.One complex world of mitochondrial parkinsonismDefective mitochondrial DNA homeostasis in the substantia nigra in Parkinson diseaseUnravelling mitochondrial pathways to Parkinson's disease.The Parkinson Disease Mitochondrial Hypothesis: Where Are We at?DRAM Is Involved in Regulating Nucleoside Analog-Induced Neuronal Autophagy in a p53-Independent Manner.Naked mole-rats maintain healthy skeletal muscle and Complex IV mitochondrial enzyme function into old age.Lack of Parkin anticipates the phenotype and affects mitochondrial morphology and mtDNA levels in a mouse model of Parkinson's Disease.Reply: DGUOK recessive mutations in patients with CPEO, mitochondrial myopathy, parkinsonism and mtDNA deletions.Oxygen Concentration and Oxidative Stress Modulate the Influence of Alzheimer's Disease Aβ1-42 Peptide on Human Cells.Current perspective of mitochondrial biology in Parkinson's disease.Environmental and Genetic Variables Influencing Mitochondrial Health and Parkinson's Disease Penetrance.Mitochondrial Quality Control in Neurodegenerative Diseases: Focus on Parkinson's Disease and Huntington's Disease.Mitochondrial Targeting in Neurodegeneration: A Heme PerspectiveDefective mitochondrial protein import contributes to complex I-induced mitochondrial dysfunction and neurodegeneration in Parkinson's diseaseModeling Parkinson's Disease Using Patient-specific Induced Pluripotent Stem Cells
P2860
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P2860
Accumulation of mitochondrial DNA deletions within dopaminergic neurons triggers neuroprotective mechanisms.
description
2013 nî lūn-bûn
@nan
2013 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
Accumulation of mitochondrial ...... rs neuroprotective mechanisms.
@ast
Accumulation of mitochondrial ...... rs neuroprotective mechanisms.
@en
Accumulation of mitochondrial ...... rs neuroprotective mechanisms.
@nl
type
label
Accumulation of mitochondrial ...... rs neuroprotective mechanisms.
@ast
Accumulation of mitochondrial ...... rs neuroprotective mechanisms.
@en
Accumulation of mitochondrial ...... rs neuroprotective mechanisms.
@nl
prefLabel
Accumulation of mitochondrial ...... rs neuroprotective mechanisms.
@ast
Accumulation of mitochondrial ...... rs neuroprotective mechanisms.
@en
Accumulation of mitochondrial ...... rs neuroprotective mechanisms.
@nl
P2093
P2860
P356
P1433
P1476
Accumulation of mitochondrial ...... rs neuroprotective mechanisms.
@en
P2093
Andreas Bender
Antoni L Andreu
Celine Perier
Christoph Laub
Elena García-Arumí
Jordi Bové
Ma Jesus Melià
Matthias Elstner
Miquel Vila
Peter Teismann
P2860
P304
P356
10.1093/BRAIN/AWT196
P407
P577
2013-08-01T00:00:00Z