Mitochondrial DNA homeostasis is essential for nigrostriatal integrity

This publication has 22 references indexed in Scilit:

• Syndromic parkinsonism and dementia associated with OPA1 missense mutations
  Annals of Neurology, 2015
• Detailed analysis of mitochondrial respiratory chain defects caused by loss of PINK1
  Neuroscience Letters, 2014
• Neuron-Specific Mitochondrial DNA Deletion Levels in Sporadic Alzheimer´s Disease
  Current Alzheimer Research, 2013
• Parkinson's Disease and Parkinsonism: Neuropathology
  Cold Spring Harbor Perspectives in Medicine, 2012
• Proposal for the standardisation of multi-centre trials in nuclear medicine imaging: prerequisites for a European 123I-FP-CIT SPECT database
  European Journal of Nuclear Medicine and Molecular Imaging, 2011
• Mitochondrial DNA deletions and neurodegeneration in multiple sclerosis
  Annals of Neurology, 2010
• Infantile-onset spinocerebellar ataxia and mitochondrial recessive ataxia syndrome are associated with neuronal complex I defect and mtDNA depletion
  Human Molecular Genetics, 2008
• The impact of mitochondrial tRNA mutations on the amount of ATP synthase differs in the brain compared to other tissues
  Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, 2008
• Mitochondrial DNA deletions are abundant and cause functional impairment in aged human substantia nigra neurons
  Nature Genetics, 2006
• High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease
  Nature Genetics, 2006