Pink, parkin and the brain
- 28 June 2006
- journal article
- editorial
- Published by Springer Nature in Nature
- Vol. 441 (7097) , 1058
- https://doi.org/10.1038/4411058a
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- Homozygous and heterozygous PINK1 mutations: Considerations for diagnosis and care of Parkinson's disease patientsMovement Disorders, 2006
- Mitochondrial dysfunction in Drosophila PINK1 mutants is complemented by parkinNature, 2006
- Drosophila pink1 is required for mitochondrial function and interacts genetically with parkinNature, 2006
- How genetics research in Parkinson's disease is enhancing understanding of the common idiopathic forms of the diseaseCurrent Opinion in Neurology, 2005
- Hereditary Early-Onset Parkinson's Disease Caused by Mutations in PINK1Science, 2004
- Mitochondrial Dysfunction and Oxidative Damage in parkin-deficient MiceJournal of Biological Chemistry, 2004
- Mitochondrial complex I and IV activities in leukocytes from patients with parkin mutationsMovement Disorders, 2003
- Mitochondrial pathology and apoptotic muscle degeneration in Drosophila parkin mutantsProceedings of the National Academy of Sciences, 2003
- Parkin prevents mitochondrial swelling and cytochrome c release in mitochondria-dependent cell deathHuman Molecular Genetics, 2003
- Complex I and Parkinson's DiseaseIUBMB Life, 2001