No association between common POLG1 variants and sporadic idiopathic Parkinson's disease
Identifieur interne : 002181 ( Main/Exploration ); précédent : 002180; suivant : 002182No association between common POLG1 variants and sporadic idiopathic Parkinson's disease
Auteurs : Gavin Hudson [Royaume-Uni] ; Watcharee Tiangyou [Royaume-Uni] ; Andrea Stutt [Royaume-Uni] ; Martin Eccles [Royaume-Uni] ; Louise Robinson [Royaume-Uni] ; David J. Burn [Royaume-Uni] ; Patrick F. Chinnery [Royaume-Uni]Source :
- Movement Disorders [ 0885-3185 ] ; 2009-05-15.
English descriptors
- KwdEn :
- MESH :
- chemical , genetics : DNA-Directed DNA Polymerase.
- genetics : Genetic Variation, Parkinson Disease.
- statistics & numerical data : Residence Characteristics.
- Aged, Female, Gene Frequency, Genotype, Humans, Male, Middle Aged.
Url:
DOI: 10.1002/mds.22310
Affiliations:
Links toward previous steps (curation, corpus...)
- to stream Istex, to step Corpus: 002200
- to stream Istex, to step Curation: 002200
- to stream Istex, to step Checkpoint: 000D83
- to stream PubMed, to step Corpus: 001D99
- to stream PubMed, to step Curation: 001D99
- to stream PubMed, to step Checkpoint: 001C88
- to stream Ncbi, to step Merge: 002578
- to stream Ncbi, to step Curation: 002578
- to stream Ncbi, to step Checkpoint: 002578
- to stream Main, to step Merge: 002A42
- to stream Main, to step Curation: 002181
Le document en format XML
<record><TEI wicri:istexFullTextTei="biblStruct"><teiHeader><fileDesc><titleStmt><title xml:lang="en">No association between common POLG1 variants and sporadic idiopathic Parkinson's disease</title>
<author><name sortKey="Hudson, Gavin" sort="Hudson, Gavin" uniqKey="Hudson G" first="Gavin" last="Hudson">Gavin Hudson</name>
</author>
<author><name sortKey="Tiangyou, Watcharee" sort="Tiangyou, Watcharee" uniqKey="Tiangyou W" first="Watcharee" last="Tiangyou">Watcharee Tiangyou</name>
</author>
<author><name sortKey="Stutt, Andrea" sort="Stutt, Andrea" uniqKey="Stutt A" first="Andrea" last="Stutt">Andrea Stutt</name>
</author>
<author><name sortKey="Eccles, Martin" sort="Eccles, Martin" uniqKey="Eccles M" first="Martin" last="Eccles">Martin Eccles</name>
</author>
<author><name sortKey="Robinson, Louise" sort="Robinson, Louise" uniqKey="Robinson L" first="Louise" last="Robinson">Louise Robinson</name>
</author>
<author><name sortKey="Burn, David J" sort="Burn, David J" uniqKey="Burn D" first="David J." last="Burn">David J. Burn</name>
</author>
<author><name sortKey="Chinnery, Patrick F" sort="Chinnery, Patrick F" uniqKey="Chinnery P" first="Patrick F." last="Chinnery">Patrick F. Chinnery</name>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">ISTEX</idno>
<idno type="RBID">ISTEX:EB7E0C791710AD1283024516B49CC57A01C0C2B2</idno>
<date when="2009" year="2009">2009</date>
<idno type="doi">10.1002/mds.22310</idno>
<idno type="url">https://api.istex.fr/document/EB7E0C791710AD1283024516B49CC57A01C0C2B2/fulltext/pdf</idno>
<idno type="wicri:Area/Istex/Corpus">002200</idno>
<idno type="wicri:Area/Istex/Curation">002200</idno>
<idno type="wicri:Area/Istex/Checkpoint">000D83</idno>
<idno type="wicri:doubleKey">0885-3185:2009:Hudson G:no:association:between</idno>
<idno type="wicri:source">PubMed</idno>
<idno type="RBID">pubmed:19243043</idno>
<idno type="wicri:Area/PubMed/Corpus">001D99</idno>
<idno type="wicri:Area/PubMed/Curation">001D99</idno>
<idno type="wicri:Area/PubMed/Checkpoint">001C88</idno>
<idno type="wicri:Area/Ncbi/Merge">002578</idno>
<idno type="wicri:Area/Ncbi/Curation">002578</idno>
<idno type="wicri:Area/Ncbi/Checkpoint">002578</idno>
<idno type="wicri:Area/Main/Merge">002A42</idno>
<idno type="wicri:Area/Main/Curation">002181</idno>
<idno type="wicri:Area/Main/Exploration">002181</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">No association between common POLG1 variants and sporadic idiopathic Parkinson's disease</title>
<author><name sortKey="Hudson, Gavin" sort="Hudson, Gavin" uniqKey="Hudson G" first="Gavin" last="Hudson">Gavin Hudson</name>
<affiliation wicri:level="1"><country xml:lang="fr">Royaume-Uni</country>
<wicri:regionArea>Mitochondrial Research Group, University of Newcastle Upon Tyne</wicri:regionArea>
<wicri:noRegion>University of Newcastle Upon Tyne</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Tiangyou, Watcharee" sort="Tiangyou, Watcharee" uniqKey="Tiangyou W" first="Watcharee" last="Tiangyou">Watcharee Tiangyou</name>
<affiliation wicri:level="1"><country xml:lang="fr">Royaume-Uni</country>
<wicri:regionArea>Mitochondrial Research Group, University of Newcastle Upon Tyne</wicri:regionArea>
<wicri:noRegion>University of Newcastle Upon Tyne</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Stutt, Andrea" sort="Stutt, Andrea" uniqKey="Stutt A" first="Andrea" last="Stutt">Andrea Stutt</name>
<affiliation wicri:level="1"><country xml:lang="fr">Royaume-Uni</country>
<wicri:regionArea>Institute for Ageing and Health, University of Newcastle Upon Tyne</wicri:regionArea>
<wicri:noRegion>University of Newcastle Upon Tyne</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Eccles, Martin" sort="Eccles, Martin" uniqKey="Eccles M" first="Martin" last="Eccles">Martin Eccles</name>
<affiliation wicri:level="1"><country xml:lang="fr">Royaume-Uni</country>
<wicri:regionArea>Institute for Health and Society, University of Newcastle Upon Tyne</wicri:regionArea>
<wicri:noRegion>University of Newcastle Upon Tyne</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Robinson, Louise" sort="Robinson, Louise" uniqKey="Robinson L" first="Louise" last="Robinson">Louise Robinson</name>
<affiliation wicri:level="1"><country xml:lang="fr">Royaume-Uni</country>
<wicri:regionArea>Institute for Health and Society, University of Newcastle Upon Tyne</wicri:regionArea>
<wicri:noRegion>University of Newcastle Upon Tyne</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Burn, David J" sort="Burn, David J" uniqKey="Burn D" first="David J." last="Burn">David J. Burn</name>
<affiliation wicri:level="1"><country xml:lang="fr">Royaume-Uni</country>
<wicri:regionArea>Institute for Ageing and Health, University of Newcastle Upon Tyne</wicri:regionArea>
<wicri:noRegion>University of Newcastle Upon Tyne</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Chinnery, Patrick F" sort="Chinnery, Patrick F" uniqKey="Chinnery P" first="Patrick F." last="Chinnery">Patrick F. Chinnery</name>
<affiliation wicri:level="1"><country xml:lang="fr">Royaume-Uni</country>
<wicri:regionArea>Institute for Ageing and Health, University of Newcastle Upon Tyne</wicri:regionArea>
<wicri:noRegion>University of Newcastle Upon Tyne</wicri:noRegion>
</affiliation>
<affiliation wicri:level="1"><country xml:lang="fr">Royaume-Uni</country>
<wicri:regionArea>Institute for Ageing and Health, University of Newcastle Upon Tyne</wicri:regionArea>
<wicri:noRegion>University of Newcastle Upon Tyne</wicri:noRegion>
</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="2009-05-15">2009-05-15</date>
<biblScope unit="vol">24</biblScope>
<biblScope unit="issue">7</biblScope>
<biblScope unit="page" from="1092">1092</biblScope>
<biblScope unit="page" to="1094">1094</biblScope>
</imprint>
<idno type="ISSN">0885-3185</idno>
</series>
<idno type="istex">EB7E0C791710AD1283024516B49CC57A01C0C2B2</idno>
<idno type="DOI">10.1002/mds.22310</idno>
<idno type="ArticleID">MDS22310</idno>
</biblStruct>
</sourceDesc>
<seriesStmt><idno type="ISSN">0885-3185</idno>
</seriesStmt>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Aged</term>
<term>DNA-Directed DNA Polymerase (genetics)</term>
<term>Female</term>
<term>Gene Frequency</term>
<term>Genetic Variation (genetics)</term>
<term>Genotype</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Parkinson Disease (genetics)</term>
<term>Residence Characteristics (statistics & numerical data)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>DNA-Directed DNA Polymerase</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Genetic Variation</term>
<term>Parkinson Disease</term>
</keywords>
<keywords scheme="MESH" qualifier="statistics & numerical data" xml:lang="en"><term>Residence Characteristics</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Aged</term>
<term>Female</term>
<term>Gene Frequency</term>
<term>Genotype</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
</keywords>
</textClass>
<langUsage><language ident="en">en</language>
</langUsage>
</profileDesc>
</teiHeader>
</TEI>
<affiliations><list><country><li>Royaume-Uni</li>
</country>
</list>
<tree><country name="Royaume-Uni"><noRegion><name sortKey="Hudson, Gavin" sort="Hudson, Gavin" uniqKey="Hudson G" first="Gavin" last="Hudson">Gavin Hudson</name>
</noRegion>
<name sortKey="Burn, David J" sort="Burn, David J" uniqKey="Burn D" first="David J." last="Burn">David J. Burn</name>
<name sortKey="Chinnery, Patrick F" sort="Chinnery, Patrick F" uniqKey="Chinnery P" first="Patrick F." last="Chinnery">Patrick F. Chinnery</name>
<name sortKey="Chinnery, Patrick F" sort="Chinnery, Patrick F" uniqKey="Chinnery P" first="Patrick F." last="Chinnery">Patrick F. Chinnery</name>
<name sortKey="Eccles, Martin" sort="Eccles, Martin" uniqKey="Eccles M" first="Martin" last="Eccles">Martin Eccles</name>
<name sortKey="Robinson, Louise" sort="Robinson, Louise" uniqKey="Robinson L" first="Louise" last="Robinson">Louise Robinson</name>
<name sortKey="Stutt, Andrea" sort="Stutt, Andrea" uniqKey="Stutt A" first="Andrea" last="Stutt">Andrea Stutt</name>
<name sortKey="Tiangyou, Watcharee" sort="Tiangyou, Watcharee" uniqKey="Tiangyou W" first="Watcharee" last="Tiangyou">Watcharee Tiangyou</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 002181 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd -nk 002181 | 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:EB7E0C791710AD1283024516B49CC57A01C0C2B2 |texte= No association between common POLG1 variants and sporadic idiopathic Parkinson's disease }}
This area was generated with Dilib version V0.6.23. |