Molecular pathophysiology of Parkinson's disease.

Published

Book

Parkinson's disease (PD) is a progressive neurodegenerative movement disorder that results primarily from the death of dopaminergic neurons in the substantia nigra. Although the etiology of PD is incompletely understood, the recent discovery of genes associated with rare monogenic forms of the disease, together with earlier studies and new experimental animal models, has provided important and novel insight into the molecular pathways involved in disease pathogenesis. Increasing evidence indicates that deficits in mitochondrial function, oxidative and nitrosative stress, the accumulation of aberrant or misfolded proteins, and ubiquitin-proteasome system dysfunction may represent the principal molecular pathways or events that commonly underlie the pathogenesis of sporadic and familial forms of PD .

Full Text

Duke Authors

Cited Authors

  • Moore, DJ; West, AB; Dawson, VL; Dawson, TM

Published Date

  • January 2005

Volume / Issue

  • 28 /

Start / End Page

  • 57 - 87

PubMed ID

  • 16022590

Pubmed Central ID

  • 16022590

Digital Object Identifier (DOI)

  • 10.1146/annurev.neuro.28.061604.135718