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pubmed-article:15076711pubmed:abstractTextOne possible cause for the neuronal loss in sporadic amyotrophic lateral sclerosis (S-ALS) is an increase of free radicals, which may produce oxidative damage to susceptible biomolecules, which, in turn, can damage the mitochondrial DNA (mtDNA). Following laser microdissection of single motor neurons from paraffin-embedded autopsy tissue, we analyzed the presence of a common mtDNA deletion, the 5 kb common deletion (CD). Spinal cord neurons showed slightly higher CD detection rate in patients than controls (94% vs 75%). No significant differences were found between patients and controls for neurons derived from other motor or non-motor regions. A PCR assay of serial DNA dilutions (10-fold) showed no CD level differences between motor neurons in S-ALS and controls. These data suggest that neuronal death in S-ALS is not associated with significant accumulation of mtDNA deletions.lld:pubmed
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pubmed-article:15076711pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:15076711pubmed:articleTitleSingle-cell analysis of mtDNA deletion levels in sporadic amyotrophic lateral sclerosis.lld:pubmed
pubmed-article:15076711pubmed:affiliationDepartment of Neuropathology, Otto-von-Guericke-University, Leipziger Strasse 44, D-39120 Magdeburg, Germany. Christian.Marwin@Medizin.Uni-Magdeburg.delld:pubmed
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