Interleukin‐1A (−889) genetic polymorphism increases the risk of multiple system atrophy
Identifieur interne : 002990 ( Istex/Checkpoint ); précédent : 002989; suivant : 002991Interleukin‐1A (−889) genetic polymorphism increases the risk of multiple system atrophy
Auteurs : Onofre Combarros [Espagne] ; Jon Infante [Espagne] ; Javier Llorca [Espagne] ; José Berciano [Espagne]Source :
- Movement Disorders [ 0885-3185 ] ; 2003-11.
English descriptors
- KwdEn :
Abstract
In a case‐control study using a clinically well‐defined group of 30 multiple system atrophy (MSA) patients and 110 control subjects, homozygosity for interleukin‐1A (IL‐1A) allele 2 (high secretor of proinflammatory cytokine) in the regulatory region (‐889) of the IL‐1A gene was associated with a fivefold increased risk for MSA. © 2003 Movement Disorder Society
Url:
DOI: 10.1002/mds.10540
Affiliations:
Links toward previous steps (curation, corpus...)
Links to Exploration step
ISTEX:EA0122126C20CDFB90F8EF625D60F95ED90A83E1Le document en format XML
<record><TEI wicri:istexFullTextTei="biblStruct"><teiHeader><fileDesc><titleStmt><title xml:lang="en">Interleukin‐1A (−889) genetic polymorphism increases the risk of multiple system atrophy</title>
<author><name sortKey="Combarros, Onofre" sort="Combarros, Onofre" uniqKey="Combarros O" first="Onofre" last="Combarros">Onofre Combarros</name>
</author>
<author><name sortKey="Infante, Jon" sort="Infante, Jon" uniqKey="Infante J" first="Jon" last="Infante">Jon Infante</name>
</author>
<author><name sortKey="Llorca, Javier" sort="Llorca, Javier" uniqKey="Llorca J" first="Javier" last="Llorca">Javier Llorca</name>
</author>
<author><name sortKey="Berciano, Jose" sort="Berciano, Jose" uniqKey="Berciano J" first="José" last="Berciano">José Berciano</name>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">ISTEX</idno>
<idno type="RBID">ISTEX:EA0122126C20CDFB90F8EF625D60F95ED90A83E1</idno>
<date when="2003" year="2003">2003</date>
<idno type="doi">10.1002/mds.10540</idno>
<idno type="url">https://api.istex.fr/document/EA0122126C20CDFB90F8EF625D60F95ED90A83E1/fulltext/pdf</idno>
<idno type="wicri:Area/Istex/Corpus">003A23</idno>
<idno type="wicri:Area/Istex/Curation">003A23</idno>
<idno type="wicri:Area/Istex/Checkpoint">002990</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">Interleukin‐1A (−889) genetic polymorphism increases the risk of multiple system atrophy</title>
<author><name sortKey="Combarros, Onofre" sort="Combarros, Onofre" uniqKey="Combarros O" first="Onofre" last="Combarros">Onofre Combarros</name>
<affiliation wicri:level="1"><country xml:lang="fr">Espagne</country>
<wicri:regionArea>Neurology Service, University Hospital Marqués de Valdecilla, University of Cantabria, Santander</wicri:regionArea>
<wicri:noRegion>Santander</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Infante, Jon" sort="Infante, Jon" uniqKey="Infante J" first="Jon" last="Infante">Jon Infante</name>
<affiliation wicri:level="1"><country xml:lang="fr">Espagne</country>
<wicri:regionArea>Neurology Service, University Hospital Marqués de Valdecilla, University of Cantabria, Santander</wicri:regionArea>
<wicri:noRegion>Santander</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Llorca, Javier" sort="Llorca, Javier" uniqKey="Llorca J" first="Javier" last="Llorca">Javier Llorca</name>
<affiliation wicri:level="1"><country xml:lang="fr">Espagne</country>
<wicri:regionArea>Division of Preventive Medicine, University of Cantabria School of Medicine, Santander</wicri:regionArea>
<wicri:noRegion>Santander</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Berciano, Jose" sort="Berciano, Jose" uniqKey="Berciano J" first="José" last="Berciano">José Berciano</name>
<affiliation wicri:level="1"><country xml:lang="fr">Espagne</country>
<wicri:regionArea>Neurology Service, University Hospital Marqués de Valdecilla, University of Cantabria, Santander</wicri:regionArea>
<wicri:noRegion>Santander</wicri:noRegion>
</affiliation>
</author>
</analytic>
<monogr></monogr>
<series><title level="j">Movement Disorders</title>
<title level="j" type="sub">Official Journal of the Movement Disorder Society</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="2003-11">2003-11</date>
<biblScope unit="vol">18</biblScope>
<biblScope unit="issue">11</biblScope>
<biblScope unit="page" from="1385">1385</biblScope>
<biblScope unit="page" to="1386">1386</biblScope>
</imprint>
<idno type="ISSN">0885-3185</idno>
</series>
<idno type="istex">EA0122126C20CDFB90F8EF625D60F95ED90A83E1</idno>
<idno type="DOI">10.1002/mds.10540</idno>
<idno type="ArticleID">MDS10540</idno>
</biblStruct>
</sourceDesc>
<seriesStmt><idno type="ISSN">0885-3185</idno>
</seriesStmt>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>IL‐1A</term>
<term>multiple system atrophy</term>
<term>polymorphism</term>
</keywords>
</textClass>
<langUsage><language ident="en">en</language>
</langUsage>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">In a case‐control study using a clinically well‐defined group of 30 multiple system atrophy (MSA) patients and 110 control subjects, homozygosity for interleukin‐1A (IL‐1A) allele 2 (high secretor of proinflammatory cytokine) in the regulatory region (‐889) of the IL‐1A gene was associated with a fivefold increased risk for MSA. © 2003 Movement Disorder Society</div>
</front>
</TEI>
<affiliations><list><country><li>Espagne</li>
</country>
</list>
<tree><country name="Espagne"><noRegion><name sortKey="Combarros, Onofre" sort="Combarros, Onofre" uniqKey="Combarros O" first="Onofre" last="Combarros">Onofre Combarros</name>
</noRegion>
<name sortKey="Berciano, Jose" sort="Berciano, Jose" uniqKey="Berciano J" first="José" last="Berciano">José Berciano</name>
<name sortKey="Infante, Jon" sort="Infante, Jon" uniqKey="Infante J" first="Jon" last="Infante">Jon Infante</name>
<name sortKey="Llorca, Javier" sort="Llorca, Javier" uniqKey="Llorca J" first="Javier" last="Llorca">Javier Llorca</name>
</country>
</tree>
</affiliations>
</record>
Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Santé/explor/MovDisordV3/Data/Istex/Checkpoint
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 002990 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Istex/Checkpoint/biblio.hfd -nk 002990 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien |wiki= Wicri/Santé |area= MovDisordV3 |flux= Istex |étape= Checkpoint |type= RBID |clé= ISTEX:EA0122126C20CDFB90F8EF625D60F95ED90A83E1 |texte= Interleukin‐1A (−889) genetic polymorphism increases the risk of multiple system atrophy }}
This area was generated with Dilib version V0.6.23. |