Serveur d'exploration sur la maladie de Parkinson

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Recessive Parkinson's disease

Identifieur interne : 000C59 ( Main/Corpus ); précédent : 000C58; suivant : 000C60

Recessive Parkinson's disease

Auteurs : Shin-Ichiro Kubo ; Nobutaka Hattori ; Yoshikuni Mizuno

Source :

RBID : ISTEX:11A1C677F7100DB04F91F2EF9CE3CBB879261529

English descriptors

Abstract

Parkinson's disease (PD) is a progressive neurodegenerative disease caused by loss of dopaminergic neurons in the substantia nigra pars compacta. Although the etiology of PD remains unclear, it is now clear that genetic factors contribute to the pathogenesis of the disease. Recently, several causative genes have been identified in monogenic forms of PD. Accumulating evidence indicates that their gene products play important roles in mitochondrial function, oxidative stress response, and the ubiquitin–proteasome system, which are also implicated in sporadic PD, suggesting that these gene products share a common pathway to nigral degeneration in both familial and sporadic PD. Here, we review recent advances in knowledge about genes associated with recessive PD, including parkin, PINK1, and DJ‐1. © 2006 Movement Disorder Society

Url:
DOI: 10.1002/mds.20841

Links to Exploration step

ISTEX:11A1C677F7100DB04F91F2EF9CE3CBB879261529

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<affiliation>Department of Neurology, Juntendo University School of Medicine, Tokyo, Japan</affiliation>
<affiliation>Research Institute for Diseases of Old Age, Juntendo University School of Medicine, Tokyo, Japan</affiliation>
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<dateIssued encoding="w3cdtf">2006-07</dateIssued>
<dateCaptured encoding="w3cdtf">2005-07-21</dateCaptured>
<dateValid encoding="w3cdtf">2005-10-03</dateValid>
<copyrightDate encoding="w3cdtf">2006</copyrightDate>
</originInfo>
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<languageTerm type="code" authority="rfc3066">en</languageTerm>
<languageTerm type="code" authority="iso639-2b">eng</languageTerm>
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<abstract lang="en">Parkinson's disease (PD) is a progressive neurodegenerative disease caused by loss of dopaminergic neurons in the substantia nigra pars compacta. Although the etiology of PD remains unclear, it is now clear that genetic factors contribute to the pathogenesis of the disease. Recently, several causative genes have been identified in monogenic forms of PD. Accumulating evidence indicates that their gene products play important roles in mitochondrial function, oxidative stress response, and the ubiquitin–proteasome system, which are also implicated in sporadic PD, suggesting that these gene products share a common pathway to nigral degeneration in both familial and sporadic PD. Here, we review recent advances in knowledge about genes associated with recessive PD, including parkin, PINK1, and DJ‐1. © 2006 Movement Disorder Society</abstract>
<subject lang="en">
<genre>Keywords</genre>
<topic>parkin</topic>
<topic>PINK1</topic>
<topic>DJ‐1</topic>
<topic>recessive Parkinson's disease</topic>
<topic>mitochondria</topic>
<topic>oxidative stress</topic>
<topic>ubiquitin–proteasome system</topic>
</subject>
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<title>Movement Disorders</title>
<subTitle>Official Journal of the Movement Disorder Society</subTitle>
</titleInfo>
<titleInfo type="abbreviated">
<title>Mov. Disord.</title>
</titleInfo>
<genre type="Journal">journal</genre>
<subject>
<genre>article category</genre>
<topic>Research Review</topic>
</subject>
<identifier type="ISSN">0885-3185</identifier>
<identifier type="eISSN">1531-8257</identifier>
<identifier type="DOI">10.1002/(ISSN)1531-8257</identifier>
<identifier type="PublisherID">MDS</identifier>
<part>
<date>2006</date>
<detail type="volume">
<caption>vol.</caption>
<number>21</number>
</detail>
<detail type="issue">
<caption>no.</caption>
<number>7</number>
</detail>
<extent unit="pages">
<start>885</start>
<end>893</end>
<total>9</total>
</extent>
</part>
</relatedItem>
<identifier type="istex">11A1C677F7100DB04F91F2EF9CE3CBB879261529</identifier>
<identifier type="DOI">10.1002/mds.20841</identifier>
<identifier type="ArticleID">MDS20841</identifier>
<accessCondition type="use and reproduction" contentType="copyright">Copyright © 2006 Movement Disorder Society</accessCondition>
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<recordContentSource>WILEY</recordContentSource>
<recordOrigin>Wiley Subscription Services, Inc., A Wiley Company</recordOrigin>
</recordInfo>
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