The role of parkin in familial and sporadic Parkinson's disease
Identifieur interne : 001949 ( Main/Exploration ); précédent : 001948; suivant : 001950The role of parkin in familial and sporadic Parkinson's disease
Auteurs : Ted M. Dawson [États-Unis] ; Valina L. Dawson [États-Unis]Source :
- Movement Disorders [ 0885-3185 ] ; 2010.
Descripteurs français
- Pascal (Inist)
English descriptors
- KwdEn :
- AIMP2, Animals, FBP‐1, Familial disease, Humans, Mitochondria, Mitochondria (metabolism), Multicatalytic endopeptidase complex, Mutation (genetics), Nervous system diseases, PINK1, Parkin, Parkinson Disease (classification), Parkinson Disease (genetics), Parkinson Disease (metabolism), Parkinson Disease (pathology), Parkinson disease, Sporadic, Ubiquitin, Ubiquitin-Protein Ligases (genetics), Ubiquitin-Protein Ligases (metabolism), mitochondria, proteasome, ubiquitin.
- MESH :
- chemical , genetics : Ubiquitin-Protein Ligases.
- classification : Parkinson Disease.
- genetics : Mutation, Parkinson Disease.
- metabolism : Mitochondria, Parkinson Disease, Ubiquitin-Protein Ligases.
- pathology : Parkinson Disease.
- Animals, Humans.
Abstract
Mutations in parkin are the second most common known cause of Parkinson's disease (PD). Parkin is an ubiquitin E3 ligase that monoubiquitinates and polyubiquitinates proteins to regulate a variety of cellular processes. Loss of parkin's E3 ligase activity is thought to play a pathogenic role in both inherited and sporadic PD. Here, we review parkin biology and pathobiology and its role in the pathogenesis of PD. © 2010 Movement Disorder Society
Url:
- https://api.istex.fr/document/574280DDE25B1A05218AFEE387A41ECAF43B80AD/fulltext/pdf
- http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4115293
DOI: 10.1002/mds.22798
Affiliations:
Links toward previous steps (curation, corpus...)
- to stream Istex, to step Corpus: 001B84
- to stream Istex, to step Curation: 001B84
- to stream Istex, to step Checkpoint: 000628
- to stream Pmc, to step Corpus: 000218
- to stream Pmc, to step Curation: 000218
- to stream Pmc, to step Checkpoint: 000298
- to stream PubMed, to step Corpus: 001943
- to stream PubMed, to step Curation: 001943
- to stream PubMed, to step Checkpoint: 001555
- to stream Ncbi, to step Merge: 002A59
- to stream Ncbi, to step Curation: 002A59
- to stream Ncbi, to step Checkpoint: 002A59
- to stream Main, to step Merge: 001D85
- to stream PascalFrancis, to step Corpus: 000B92
- to stream PascalFrancis, to step Curation: 002127
- to stream PascalFrancis, to step Checkpoint: 000784
- to stream Main, to step Merge: 002371
- to stream Main, to step Curation: 001949
Le document en format XML
<record><TEI wicri:istexFullTextTei="biblStruct"><teiHeader><fileDesc><titleStmt><title xml:lang="en">The role of parkin in familial and sporadic Parkinson's disease</title>
<author><name sortKey="Dawson, Ted M" sort="Dawson, Ted M" uniqKey="Dawson T" first="Ted M." last="Dawson">Ted M. Dawson</name>
</author>
<author><name sortKey="Dawson, Valina L" sort="Dawson, Valina L" uniqKey="Dawson V" first="Valina L." last="Dawson">Valina L. Dawson</name>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">ISTEX</idno>
<idno type="RBID">ISTEX:574280DDE25B1A05218AFEE387A41ECAF43B80AD</idno>
<date when="2010" year="2010">2010</date>
<idno type="doi">10.1002/mds.22798</idno>
<idno type="url">https://api.istex.fr/document/574280DDE25B1A05218AFEE387A41ECAF43B80AD/fulltext/pdf</idno>
<idno type="wicri:Area/Istex/Corpus">001B84</idno>
<idno type="wicri:Area/Istex/Curation">001B84</idno>
<idno type="wicri:Area/Istex/Checkpoint">000628</idno>
<idno type="wicri:doubleKey">0885-3185:2010:Dawson T:the:role:of</idno>
<idno type="wicri:source">PMC</idno>
<idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4115293</idno>
<idno type="RBID">PMC:4115293</idno>
<idno type="wicri:Area/Pmc/Corpus">000218</idno>
<idno type="wicri:Area/Pmc/Curation">000218</idno>
<idno type="wicri:Area/Pmc/Checkpoint">000298</idno>
<idno type="wicri:source">PubMed</idno>
<idno type="wicri:Area/PubMed/Corpus">001943</idno>
<idno type="wicri:Area/PubMed/Curation">001943</idno>
<idno type="wicri:Area/PubMed/Checkpoint">001555</idno>
<idno type="wicri:Area/Ncbi/Merge">002A59</idno>
<idno type="wicri:Area/Ncbi/Curation">002A59</idno>
<idno type="wicri:Area/Ncbi/Checkpoint">002A59</idno>
<idno type="wicri:doubleKey">0885-3185:2010:Dawson T:the:role:of</idno>
<idno type="wicri:Area/Main/Merge">001D85</idno>
<idno type="wicri:source">INIST</idno>
<idno type="RBID">Pascal:10-0193453</idno>
<idno type="wicri:Area/PascalFrancis/Corpus">000B92</idno>
<idno type="wicri:Area/PascalFrancis/Curation">002127</idno>
<idno type="wicri:Area/PascalFrancis/Checkpoint">000784</idno>
<idno type="wicri:doubleKey">0885-3185:2010:Dawson T:the:role:of</idno>
<idno type="wicri:Area/Main/Merge">002371</idno>
<idno type="wicri:Area/Main/Curation">001949</idno>
<idno type="wicri:Area/Main/Exploration">001949</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">The role of parkin in familial and sporadic Parkinson's disease</title>
<author><name sortKey="Dawson, Ted M" sort="Dawson, Ted M" uniqKey="Dawson T" first="Ted M." last="Dawson">Ted M. Dawson</name>
<affiliation wicri:level="2"><country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Neuroregeneration and Stem Cell Programs, Institute for Cell Engineering, Johns Hopkins University School of Medicine, Baltimore, Maryland</wicri:regionArea>
<placeName><region type="state">Maryland</region>
</placeName>
</affiliation>
<affiliation wicri:level="2"><country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, Maryland</wicri:regionArea>
<placeName><region type="state">Maryland</region>
</placeName>
</affiliation>
<affiliation wicri:level="2"><country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Solomon H. Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, Maryland</wicri:regionArea>
<placeName><region type="state">Maryland</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Dawson, Valina L" sort="Dawson, Valina L" uniqKey="Dawson V" first="Valina L." last="Dawson">Valina L. Dawson</name>
<affiliation wicri:level="2"><country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Neuroregeneration and Stem Cell Programs, Institute for Cell Engineering, Johns Hopkins University School of Medicine, Baltimore, Maryland</wicri:regionArea>
<placeName><region type="state">Maryland</region>
</placeName>
</affiliation>
<affiliation wicri:level="2"><country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, Maryland</wicri:regionArea>
<placeName><region type="state">Maryland</region>
</placeName>
</affiliation>
<affiliation wicri:level="2"><country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Solomon H. Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, Maryland</wicri:regionArea>
<placeName><region type="state">Maryland</region>
</placeName>
</affiliation>
<affiliation wicri:level="2"><country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Physiology, Johns Hopkins University School of Medicine, Baltimore, Maryland</wicri:regionArea>
<placeName><region type="state">Maryland</region>
</placeName>
</affiliation>
</author>
</analytic>
<monogr></monogr>
<series><title level="j">Movement Disorders</title>
<title level="j" type="abbrev">Mov. Disord.</title>
<idno type="ISSN">0885-3185</idno>
<idno type="eISSN">1531-8257</idno>
<imprint><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher>
<pubPlace>Hoboken</pubPlace>
<date type="published" when="2010">2010</date>
<biblScope unit="vol">25</biblScope>
<biblScope unit="issue">S1</biblScope>
<biblScope unit="page" from="S32">S32</biblScope>
<biblScope unit="page" to="S39">S39</biblScope>
</imprint>
<idno type="ISSN">0885-3185</idno>
</series>
<idno type="istex">574280DDE25B1A05218AFEE387A41ECAF43B80AD</idno>
<idno type="DOI">10.1002/mds.22798</idno>
<idno type="ArticleID">MDS22798</idno>
</biblStruct>
</sourceDesc>
<seriesStmt><idno type="ISSN">0885-3185</idno>
</seriesStmt>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>AIMP2</term>
<term>Animals</term>
<term>FBP‐1</term>
<term>Familial disease</term>
<term>Humans</term>
<term>Mitochondria</term>
<term>Mitochondria (metabolism)</term>
<term>Multicatalytic endopeptidase complex</term>
<term>Mutation (genetics)</term>
<term>Nervous system diseases</term>
<term>PINK1</term>
<term>Parkin</term>
<term>Parkinson Disease (classification)</term>
<term>Parkinson Disease (genetics)</term>
<term>Parkinson Disease (metabolism)</term>
<term>Parkinson Disease (pathology)</term>
<term>Parkinson disease</term>
<term>Sporadic</term>
<term>Ubiquitin</term>
<term>Ubiquitin-Protein Ligases (genetics)</term>
<term>Ubiquitin-Protein Ligases (metabolism)</term>
<term>mitochondria</term>
<term>proteasome</term>
<term>ubiquitin</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Ubiquitin-Protein Ligases</term>
</keywords>
<keywords scheme="MESH" qualifier="classification" xml:lang="en"><term>Parkinson Disease</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Mutation</term>
<term>Parkinson Disease</term>
</keywords>
<keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Mitochondria</term>
<term>Parkinson Disease</term>
<term>Ubiquitin-Protein Ligases</term>
</keywords>
<keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Parkinson Disease</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Animals</term>
<term>Humans</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr"><term>Maladie de Parkinson</term>
<term>Maladie familiale</term>
<term>Mitochondrie</term>
<term>Multicatalytic endopeptidase complex</term>
<term>Parkine</term>
<term>Pathologie du système nerveux</term>
<term>Sporadique</term>
<term>Ubiquitine</term>
</keywords>
</textClass>
<langUsage><language ident="en">en</language>
</langUsage>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">Mutations in parkin are the second most common known cause of Parkinson's disease (PD). Parkin is an ubiquitin E3 ligase that monoubiquitinates and polyubiquitinates proteins to regulate a variety of cellular processes. Loss of parkin's E3 ligase activity is thought to play a pathogenic role in both inherited and sporadic PD. Here, we review parkin biology and pathobiology and its role in the pathogenesis of PD. © 2010 Movement Disorder Society</div>
</front>
</TEI>
<affiliations><list><country><li>États-Unis</li>
</country>
<region><li>Maryland</li>
</region>
</list>
<tree><country name="États-Unis"><region name="Maryland"><name sortKey="Dawson, Ted M" sort="Dawson, Ted M" uniqKey="Dawson T" first="Ted M." last="Dawson">Ted M. Dawson</name>
</region>
<name sortKey="Dawson, Ted M" sort="Dawson, Ted M" uniqKey="Dawson T" first="Ted M." last="Dawson">Ted M. Dawson</name>
<name sortKey="Dawson, Ted M" sort="Dawson, Ted M" uniqKey="Dawson T" first="Ted M." last="Dawson">Ted M. Dawson</name>
<name sortKey="Dawson, Valina L" sort="Dawson, Valina L" uniqKey="Dawson V" first="Valina L." last="Dawson">Valina L. Dawson</name>
<name sortKey="Dawson, Valina L" sort="Dawson, Valina L" uniqKey="Dawson V" first="Valina L." last="Dawson">Valina L. Dawson</name>
<name sortKey="Dawson, Valina L" sort="Dawson, Valina L" uniqKey="Dawson V" first="Valina L." last="Dawson">Valina L. Dawson</name>
<name sortKey="Dawson, Valina L" sort="Dawson, Valina L" uniqKey="Dawson V" first="Valina L." last="Dawson">Valina L. Dawson</name>
</country>
</tree>
</affiliations>
</record>
Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Santé/explor/MovDisordV3/Data/Main/Exploration
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 001949 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd -nk 001949 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien |wiki= Wicri/Santé |area= MovDisordV3 |flux= Main |étape= Exploration |type= RBID |clé= ISTEX:574280DDE25B1A05218AFEE387A41ECAF43B80AD |texte= The role of parkin in familial and sporadic Parkinson's disease }}
This area was generated with Dilib version V0.6.23. |