
Mitochondria in Parkinson Disease
Back in Fashion With a Little Help From Genetics
Miratul M. K. Muqit, MRCP;
Sonia Gandhi, MRCP;
Nicholas W. Wood, PhD, FRCP, FMedSci
Arch Neurol. 2006;63:649-654.
Parkinson disease is a devastating neurodegenerative disorder with no known cure. Impairment in mitochondrial dysfunction is thought to play a major role in the pathogenesis. Recent genetic advances suggest that mitochondrial dysfunction may be the primary defect. Drugs that target the mitochondria may therefore represent the best hope for disease-modifying therapies in Parkinson disease.
Author Affiliations: Department of Molecular Neuroscience, Institute of Neurology, University College London, London, England.
CiteULike Connotea Delicious Digg Facebook Reddit Technorati Twitter
What's this?
THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES
Paullinia cupana Mart. var. Sorbilis protects human dopaminergic neuroblastoma SH-SY5Y cell line against rotenone-induced cytotoxicity
de Oliveira et al.
Hum Exp Toxicol 2011;30:1382-1391.
ABSTRACT
Genomic variants at the PINK1 locus are associated with transcript abundance and plasma nonesterified fatty acid concentrations in European whites
Franks et al.
FASEB J. 2008;22:3135-3145.
ABSTRACT
| FULL TEXT
Spare Respiratory Capacity Rather Than Oxidative Stress Regulates Glutamate Excitotoxicity after Partial Respiratory Inhibition of Mitochondrial Complex I with Rotenone
Yadava and Nicholls
J. Neurosci. 2007;27:7310-7317.
ABSTRACT
| FULL TEXT
|