Free Radicals, Oxidative Stress and Oxidative Damage in Parkinson's Disease (original) (raw)

Increased oxidation, glycoxidation, and lipoxidation of brain proteins in prion disease

Reinald Pamplona

Free Radical Biology and Medicine, 2008

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Section: Neurotoxicology Normal Cellular Prion Protein Protects against Manganese-induced Oxidative Stress and Apoptotic Cell Death

Chris Choi

2007

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Increased levels of oxidative stress markers detected in the brains of mice devoid of prion protein

Boon Seng Wong, Robert B Petersen, George Perry

Journal of …, 2001

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Prion disease: A loss of antioxidant function?

Boon Seng Wong, Robert B Petersen

Biochemical and …, 2000

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Prion Protein-Deficient Neurons Reveal Lower Glutathione Reductase Activity and Increased Susceptibility to Hydrogen Peroxide Toxicity

Anthony White

American Journal of Pathology, 1999

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Imbalance of antioxidant defense in mice lacking cellular prion protein

FA BIO

Free Radical Biology and Medicine, 2001

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Cellular prion protein neuroprotective function: implications in prion diseases

Xavier Roucou

Journal of Molecular Medicine, 2005

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Parkinson's Disease and Alpha Synuclein: Is Parkinson's Disease a Prion-Like Disorder?

Patrik Brundin

Movement Disorders, 2013

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Oxidative stress in the brain at early preclinical stages of mouse scrapie

Michael Klein

Experimental Neurology, 2006

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Neurodegenerative Diseases: Parkinson’s and Alzheimer’s Diseases

Mikhail Kogan

Oxford Medicine Online, 2018

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Prion protein fragment PrP-(106-126) induces apoptosis via mitochondrial disruption in human neuronal SH-SY5Y cells

Deirdre Tobin

The Journal of biological chemistry, 2001

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Are oxidative stress and mitochondrial dysfunction the key players in the neurodegenerative diseases?

Domenico Nuzzo, Pier Luigi San Biagio

Free Radical Research, 2012

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Normal brain mitochondrial respiration in adult mice lacking cellular prion protein

marcelo linhares

Neuroscience Letters, 2005

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p62-Keap1-NRF2-ARE Pathway: A Contentious Player for Selective Targeting of Autophagy, Oxidative Stress and Mitochondrial Dysfunction in Prion Diseases

Tariq Hussain

Frontiers in molecular neuroscience, 2018

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Redox metals and oxidative abnormalities in human prion diseases

Robert B Petersen, George Perry

Acta Neuropathologica, 2005

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Mitochondrial dysfunction and oxidative stress in Alzheimer’s disease, and Parkinson’s disease, Huntington’s disease and Amyotrophic Lateral Sclerosis -An updated review

NIKITA KALE

Mitochondrion, 2023

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Role of Mitochondria and Oxidative Stress in Parkinson’s Disease

Cristina Carvalho

Role of Oxidative Stress in Chronic Diseases, 2014

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Neuronal death induced by misfolded prion protein is due to NAD+ depletion and can be relieved in vitro and in vivo by NAD+ replenishment

Alicia Brantley

Brain : a journal of neurology, 2015

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Protective effect of prion protein via the N-terminal region in mediating a protective effect on paraquat-induced oxidative injury in neuronal cells

Ingrid Dupiereux, Willy Zorzi, Ernst Heinen, Olivier Thellin

Journal of Neuroscience Research, 2008

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Proteinopathy, oxidative stress and mitochondrial dysfunction: cross talk in Alzheimer's disease and Parkinson's disease

Sasanka Chakrabarti

Drug design, development and therapy, 2017

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Prion Proteins Leading to Neurodegeneration

Claudio Zannoni, Giuseppe Pappalardo

Current Alzheimer Research, 2008

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Prion-induced neurotoxicity: Possible role for cell cycle activity and DNA damage response

Walker Jackson

World journal of virology, 2015

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Redox Control of Prion and Disease Pathogenesis

Neena Singh

Antioxidants & Redox Signaling, 2010

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