Spinocerebellar Ataxia Type 2 Is Associated with the Extracellular Loss of Superoxide Dismutase but Not Catalase Activity
Published 2017 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Spinocerebellar Ataxia Type 2 Is Associated with the Extracellular Loss of Superoxide Dismutase but Not Catalase Activity
Authors
Keywords
-
Journal
Frontiers in Neurology
Volume 8, Issue -, Pages -
Publisher
Frontiers Media SA
Online
2017-06-13
DOI
10.3389/fneur.2017.00276
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Evidence of oxidative stress and mitochondrial dysfunction in spinocerebellar ataxia type 2 (SCA2) patient fibroblasts: Effect of coenzyme Q10 supplementation on these parameters
- (2017) Nanna Cornelius et al. MITOCHONDRION
- Mesenchymal Stem Cells Improve Motor Functions and Decrease Neurodegeneration in Ataxic Mice
- (2015) Jonathan Jones et al. MOLECULAR THERAPY
- Direct Binding of Ataxin-2 to Distinct Elements in 3′ UTRs Promotes mRNA Stability and Protein Expression
- (2014) Moe Yokoshi et al. MOLECULAR CELL
- Consensus Paper: Pathological Mechanisms Underlying Neurodegeneration in Spinocerebellar Ataxias
- (2013) A. Matilla-Dueñas et al. CEREBELLUM
- Association between Machado–Joseph disease and oxidative stress biomarkers
- (2013) Laura Segabinazzi Pacheco et al. MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS
- Glutathione peroxidase activity is neuroprotective in models of Huntington's disease
- (2013) Robert P Mason et al. NATURE GENETICS
- Expanded ataxin-7 cause toxicity by inducing ROS production from NADPH oxidase complexes in a stable inducible Spinocerebellar ataxia type 7 (SCA7) model
- (2012) Abiodun Ajayi et al. BMC NEUROSCIENCE
- Elevated NADPH oxidase activity contributes to oxidative stress and cell death in Huntington's disease
- (2012) A. Valencia et al. HUMAN MOLECULAR GENETICS
- In Vitroandin VivoAggregation of a Fragment of Huntingtin Protein Directly Causes Free Radical Production
- (2011) Sarah Hands et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Oxidative Stress and Cell Membranes in the Pathogenesis of Alzheimer's Disease
- (2011) Paul H. Axelsen et al. PHYSIOLOGY
- The Ataxin-2 protein is required for microRNA function and synapse-specific long-term olfactory habituation
- (2011) C. McCann et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Friedreich Ataxia: Molecular Mechanisms, Redox Considerations, and Therapeutic Opportunities
- (2010) Renata Santos et al. ANTIOXIDANTS & REDOX SIGNALING
- Downregulation of NF-κB signaling by mutant huntingtin proteins induces oxidative stress and cell death
- (2010) Sami Reijonen et al. CELLULAR AND MOLECULAR LIFE SCIENCES
- Early and Late Events Induced by PolyQ-expanded Proteins
- (2010) Alessandra Bertoni et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Mesenchymal stem cell-secreted superoxide dismutase promotes cerebellar neuronal survival
- (2009) Kevin Kemp et al. JOURNAL OF NEUROCHEMISTRY
- Decreased antioxidant enzyme activity and increased mitochondrial DNA damage in cellular models of Machado-Joseph disease
- (2009) Ya-Chun Yu et al. JOURNAL OF NEUROSCIENCE RESEARCH
- Molecular epidemiology of spinocerebellar ataxias in Cuba: Insights into SCA2 founder effect in Holguin
- (2009) Luis Velázquez Pérez et al. NEUROSCIENCE LETTERS
Discover Peeref hubs
Discuss science. Find collaborators. Network.
Join a conversationAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started