Post-treatment with an ultra-low dose of NADPH oxidase inhibitor diphenyleneiodonium attenuates disease progression in multiple Parkinson’s disease models
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Title
Post-treatment with an ultra-low dose of NADPH oxidase inhibitor diphenyleneiodonium attenuates disease progression in multiple Parkinson’s disease models
Authors
Keywords
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Journal
BRAIN
Volume 138, Issue 5, Pages 1247-1262
Publisher
Oxford University Press (OUP)
Online
2015-02-26
DOI
10.1093/brain/awv034
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- Advances in the pharmacological treatment of Parkinson's disease: targeting neurotransmitter systems
- (2013) Lars Brichta et al. TRENDS IN NEUROSCIENCES
- The immunology of neurodegeneration
- (2012) Eva Czirr et al. JOURNAL OF CLINICAL INVESTIGATION
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- NSAID use and risk of Parkinson disease: a population-based case-control study
- (2011) C. Becker et al. EUROPEAN JOURNAL OF NEUROLOGY
- HMGB1 Acts on Microglia Mac1 to Mediate Chronic Neuroinflammation That Drives Progressive Neurodegeneration
- (2011) H.-M. Gao et al. JOURNAL OF NEUROSCIENCE
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- Reactive microgliosis: extracellular μ-calpain and microglia-mediated dopaminergic neurotoxicity
- (2010) Shannon Levesque et al. BRAIN
- Microglia in neurodegenerative disease
- (2010) V. Hugh Perry et al. Nature Reviews Neurology
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- NOX enzymes as novel targets for drug development
- (2008) J. David Lambeth et al. Seminars in Immunopathology
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