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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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Citations
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The environment and Parkinson's disease: is the nigrostriatal system preferentially targeted by neurotoxins?

TL;DR: Similarities between clinical and experimental findings, such as the role of pesticide exposure as a potential environmental risk factor, highlight the importance of a multidisciplinary approach to the aetiology of PD.
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Comparison between proliferative and neuron-like SH-SY5Y cells as an in vitro model for Parkinson disease studies.

TL;DR: The data suggest that SH-SY5Y cells differentiated by 7 days with the protocol described here represent a more suitable experimental model for studying the molecular and cellular mechanisms underlying the pathophysiology of PD.
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Multifunctional activities of green tea catechins in neuroprotection. Modulation of cell survival genes, iron-dependent oxidative stress and PKC signaling pathway.

TL;DR: This review will focus on the multifunctional properties of green tea and its major component (–)-epigallocatechin-3-gallate (EGCG) and their ability to induce neuroprotection and neurorescue in vitro and in vivo and their transitional metal chelating property and inhibition of oxidative stress.
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Loss of locus coeruleus neurons and reduced startle in parkin null mice

TL;DR: This mouse model will help gain a better understanding of parkin function and the mechanisms underlying parkin-associated PD, and there is a dramatic reduction of the norepinephrine-dependent startle response.
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Parkin disease: a phenotypic study of a large case series

TL;DR: A number of clinical features that can be seen in parkin disease are emphasized: focal dystonia; early instability; freezing; festination or retropulsion; concurrent autonomic failure; dramatic response to anticholinergics; early or atypical L- dopa-induced dyskinesias; exquisite sensitivity to small doses of L-dopa; and recurrent psychosis.
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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