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Journal ArticleDOI

Mutations in the DJ-1 Gene Associated with Autosomal Recessive Early-Onset Parkinsonism

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TLDR
It is shown that DJ-1 mutations are associated with PARK7, a monogenic form of human parkinsonism, and these findings indicate that loss ofDJ-1 function leads to neurodegeneration.
Abstract
The DJ-1 gene encodes a ubiquitous, highly conserved protein. Here, we show that DJ-1 mutations are associated with PARK7, a monogenic form of human parkinsonism. The function of the DJ-1 protein remains unknown, but evidence suggests its involvement in the oxidative stress response. Our findings indicate that loss of DJ-1 function leads to neurodegeneration. Elucidating the physiological role of DJ-1 protein may promote understanding of the mechanisms of brain neuronal maintenance and pathogenesis of Parkinson's disease.

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Journal ArticleDOI

The biochemistry of parkinson's disease*

TL;DR: Several genes have been identified for monogenic disorders that variably resemble Parkinson's disease, but it is not yet fully resolved how the recessive genes relate to alpha-synuclein, or whether they represent different ways to induce a similar phenotype.
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Mitochondrial dysfunction in Parkinson's disease

TL;DR: Recent research indicated that several PD-associated genes interface with pathways regulating mitochondrial function, morphology, and dynamics, and in fact, sporadic and familial PD seem to converge at the level of mitochondrial integrity.
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Diagnosis and treatment of Parkinson disease: molecules to medicine

TL;DR: Recent discoveries in the fields of diagnosis and treatment of PD are discussed and a better understanding of disease mechanisms gained through the study of monogenetic forms of PD has provided novel therapeutic targets are discussed.
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The genetic epidemiology of neurodegenerative disease

TL;DR: The current status of genetic epidemiology of the most common neurodegenerative diseases: Alzheimer disease, Parkinson disease, Lewy body dementia, frontotemporal dementia, amyotrophic lateral sclerosis, Huntington disease, and prion diseases is discussed, with a particular focus on similarities and differences among these syndromes.
References
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DJ-1, a novel oncogene which transforms mouse NIH3T3 cells in cooperation with ras.

TL;DR: DJ-1 showed a cooperative transforming activity with H-Ras, more than 3 times as strong as the activity of ras/myc combination and is suggested to be a novel mitogen-dependent oncogene product involved in a Ras-related signal transduction pathway.
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