Mitochondrial dysfunction in neurodegenerative disorders

This publication has 65 references indexed in Scilit:

• Reversible inhibition of cytochrome c oxidase, the terminal enzyme of the mitochondrial respiratory chain, by nitric oxide
  Published by Wiley ,2001
• AlaSOPro mutation in the gene encoding α-synuclein in Parkinson's disease
  Nature Genetics, 1998
• Aggregation of Huntingtin in Neuronal Intranuclear Inclusions and Dystrophic Neurites in Brain
  Science, 1997
• Respiratory deficiency due to loss of mitochondrial DNA in yeast lacking the frataxin homologue
  Nature Genetics, 1997
• Studies of human, mouse and yeast homologues indicate a mitochondrial function for frataxin
  Nature Genetics, 1997
• Mutation in the α-Synuclein Gene Identified in Families with Parkinson's Disease
  Science, 1997
• Mitochondrial respiratory chain function in multiple system atrophy
  Movement Disorders, 1997
• Exon 1 of the HD Gene with an Expanded CAG Repeat Is Sufficient to Cause a Progressive Neurological Phenotype in Transgenic Mice
  Cell, 1996
• A huntingtin-associated protein enriched in brain with implications for pathology
  Nature, 1995
• Accumulation of mtDNA with a Mutation at Position 3271 in tRNALeu(UUR) Gene Introduced from a Melas Patient to HeLa Cells Lacking mtDNA Results in Progressive Inhibition of Mitochondrial Respiratory Function
  Biochemical and Biophysical Research Communications, 1993