A candidate gene for human neurodegenerative disorders: a rat PKCγ mutation causes a Parkinsonian syndrome
- 15 October 2001
- journal article
- research article
- Published by Springer Nature in Nature Neuroscience
- Vol. 4 (11), 1061-1062
- https://doi.org/10.1038/nn740
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- Genetics of Parkinson's DiseaseAnnals of the New York Academy of Sciences, 2000
- The AS/AGU rat: a spontaneous model of disruption and degeneration in the nigrostriatal dopaminergic systemJournal of Anatomy, 2000
- Protein kinase C binding partnersBioEssays, 2000
- Parkinson's DiseaseNew England Journal of Medicine, 1998
- Activity-Dependent Regulation of [Ca2+]iin Avian Cochlear Nucleus Neurons: Roles of Protein Kinases A and C and Relation to Cell DeathJournal of Neurophysiology, 1998
- Structure of the first C2 domain of synaptotagmin I: A novel Ca2+/phospholipid-binding foldCell, 1995
- The Protein Kinase C Family for Neuronal SignalingAnnual Review of Neuroscience, 1994
- Protein kinase C isoenzymes: divergence in signal transduction?Biochemical Journal, 1993
- Postnatal development of a brain-specific subspecies of protein kinase C in ratJournal of Neuroscience, 1988
- Distribution of protein kinase C-like immunoreactive neurons in rat brainJournal of Neuroscience, 1988