Role of DJ-1 in the mechanism of pathogenesis of Parkinson's disease
LP Dolgacheva, AV Berezhnov, EI Fedotova… - Journal of Bioenergetics …, 2019 - Springer
DJ-1 protein has multiple specific mechanisms to protect dopaminergic neurons against
neurodegeneration in Parkinson's disease. Wild type DJ-1 can acts as oxidative stress …
neurodegeneration in Parkinson's disease. Wild type DJ-1 can acts as oxidative stress …
Neuroprotective Function of DJ‐1 in Parkinson's Disease
H Ariga, K Takahashi-Niki, I Kato… - Oxidative medicine …, 2013 - Wiley Online Library
Parkinson's disease (PD) is caused by dopaminergic neuronal death in the substantia nigra,
resulting in a reduced level of dopamine in the striatum. Oxidative stress and mitochondrial …
resulting in a reduced level of dopamine in the striatum. Oxidative stress and mitochondrial …
Molecular pathophysiology of Parkinson's disease
Parkinson's disease (PD) is a progressive neurodegenerative movement disorder that
results primarily from the death of dopaminergic neurons in the substantia nigra. Although …
results primarily from the death of dopaminergic neurons in the substantia nigra. Although …
The Parkinson's disease protein DJ-1 is neuroprotective due to cysteine-sulfinic acid-driven mitochondrial localization
RM Canet-Avilés, MA Wilson… - Proceedings of the …, 2004 - National Acad Sciences
Loss-of-function DJ-1 mutations can cause early-onset Parkinson's disease. The function of
DJ-1 is unknown, but an acidic isoform accumulates after oxidative stress, leading to the …
DJ-1 is unknown, but an acidic isoform accumulates after oxidative stress, leading to the …
Expanding insights of mitochondrial dysfunction in Parkinson's disease
The quest to disentangle the aetiopathogenesis of Parkinson's disease has been heavily
influenced by the genes associated with the disease. The α-synuclein-centric theory of …
influenced by the genes associated with the disease. The α-synuclein-centric theory of …
DJ‐1 has a role in antioxidative stress to prevent cell death
T Taira, Y Saito, T Niki, SMM Iguchi‐Ariga… - EMBO …, 2004 - embopress.org
Deletion and point (L166P) mutations of DJ‐1 have recently been shown to be responsible
for the onset of familial Parkinson's disease (PD, PARK7). The aim of this study was to …
for the onset of familial Parkinson's disease (PD, PARK7). The aim of this study was to …
Genetics of Parkinson disease: paradigm shifts and future prospects
MJ Farrer - Nature Reviews Genetics, 2006 - nature.com
Parkinson disease is a complex, multifactorial neurodegenerative disease. Although a
heritable basis was originally thought unlikely, recent studies have implicated several genes …
heritable basis was originally thought unlikely, recent studies have implicated several genes …
Hypersensitivity of DJ-1-deficient mice to 1-methyl-4-phenyl-1, 2, 3, 6-tetrahydropyrindine (MPTP) and oxidative stress
Mutations of the DJ-1 (PARK7) gene are linked to familial Parkinson's disease. We used
gene targeting to generate DJ-1-deficient mice that were viable, fertile, and showed no gross …
gene targeting to generate DJ-1-deficient mice that were viable, fertile, and showed no gross …
DJ-1 is a redox-dependent molecular chaperone that inhibits α-synuclein aggregate formation
S Shendelman, A Jonason, C Martinat, T Leete… - PLoS …, 2004 - journals.plos.org
Parkinson's disease (PD) pathology is characterized by the degeneration of midbrain
dopamine neurons (DNs) ultimately leading to a progressive movement disorder in patients …
dopamine neurons (DNs) ultimately leading to a progressive movement disorder in patients …
The glyoxalase pathway: the first hundred years… and beyond
M Sousa Silva, RA Gomes, AEN Ferreira… - Biochemical …, 2013 - portlandpress.com
The discovery of the enzymatic formation of lactic acid from methylglyoxal dates back to
1913 and was believed to be associated with one enzyme termed ketonaldehydemutase or …
1913 and was believed to be associated with one enzyme termed ketonaldehydemutase or …