Copyright: © 2015 Arkun K et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Objective: Our objective was to evaluate mitochondrial DNA (mtDNA) gene copy numbers in substantia nigra neurons from post-mortem Parkinson’s Disease cases and determine if the presence of Lewy bodies (LBs) altered mtDNA copy numbers or changed apparent deletion of mtDNAs. Methods: We used laser capture micro dissection to isolate neuromelanin-containing cells with or without Lewy bodies from 6 Parkinson’s Disease cases. Anti-alpha-synuclein immunohistochemistry was used to i...
AbstractA 5 kilobase deletion in mitochondrial DNA (mtDNA) has been reported to be responsible for t...
AbstractThere is a growing body of evidence linking mitochondrial dysfunction, mediated either throu...
DNA damage can cause (and result from) oxidative stress and mitochondrial impairment, both of which ...
OBJECTIVE: To determine the extent of respiratory chain abnormalities and investigate the contributi...
Increased somatic mitochondrial DNA (mtDNA) mutagenesis causes premature aging in mice, and mtDNA da...
Mitochondrial DNA (mtDNA) deletions have been investigated in a number of neurodegenerative diseases...
peer reviewedMitochondria play important roles in the regulation of key cellular processes, includin...
AbstractLike any organ, the brain is susceptible to the march of time and a reduction in mitochondri...
Mitochondria play a key role in common neurodegenerative diseases and contain their own genome: mtDN...
Mitochondria play a key role in common neurodegenerative diseases and contain their own genome: mtDN...
BACKGROUND: Deletions of the mitochondrial DNA (mtDNA) accumulate to high levels in dopaminergic neu...
Parkinson's disease (PD) is the most common neurodegenerative movement disorder, and neuroprotective...
Abstract Background Deletions of the mitochondrial DNA (mtDNA) accumulate to high levels in dopamine...
In Parkinson’s disease (PD), mitochondrial dysfunction associates with nigral dopaminergic neuronal ...
DNA damage can cause (and result from) oxidative stress and mitochondrial impairment, both of which ...
AbstractA 5 kilobase deletion in mitochondrial DNA (mtDNA) has been reported to be responsible for t...
AbstractThere is a growing body of evidence linking mitochondrial dysfunction, mediated either throu...
DNA damage can cause (and result from) oxidative stress and mitochondrial impairment, both of which ...
OBJECTIVE: To determine the extent of respiratory chain abnormalities and investigate the contributi...
Increased somatic mitochondrial DNA (mtDNA) mutagenesis causes premature aging in mice, and mtDNA da...
Mitochondrial DNA (mtDNA) deletions have been investigated in a number of neurodegenerative diseases...
peer reviewedMitochondria play important roles in the regulation of key cellular processes, includin...
AbstractLike any organ, the brain is susceptible to the march of time and a reduction in mitochondri...
Mitochondria play a key role in common neurodegenerative diseases and contain their own genome: mtDN...
Mitochondria play a key role in common neurodegenerative diseases and contain their own genome: mtDN...
BACKGROUND: Deletions of the mitochondrial DNA (mtDNA) accumulate to high levels in dopaminergic neu...
Parkinson's disease (PD) is the most common neurodegenerative movement disorder, and neuroprotective...
Abstract Background Deletions of the mitochondrial DNA (mtDNA) accumulate to high levels in dopamine...
In Parkinson’s disease (PD), mitochondrial dysfunction associates with nigral dopaminergic neuronal ...
DNA damage can cause (and result from) oxidative stress and mitochondrial impairment, both of which ...
AbstractA 5 kilobase deletion in mitochondrial DNA (mtDNA) has been reported to be responsible for t...
AbstractThere is a growing body of evidence linking mitochondrial dysfunction, mediated either throu...
DNA damage can cause (and result from) oxidative stress and mitochondrial impairment, both of which ...