MovDisordV3, Main, Exploration, bibRecord, 004060

Interleukin‐1A (−889) genetic polymorphism increases the risk of multiple system atrophy

Identifieur interne : 004060 ( Main/Exploration ); précédent : 004059; suivant : 004061

Interleukin‐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.

RBID : ISTEX:EA0122126C20CDFB90F8EF625D60F95ED90A83E1

Descripteurs français

Pascal (Inist)
- Atrophie multisystématisée, Facteur risque, Génétique, Homme, Homozygotie, Interleukine 1α, Polymorphisme.
Wicri :
- topic : Génétique, Homme.

English descriptors

KwdEn :
- Adult, Aged, Female, Genetics, Genotype, Homozygosity, Human, Humans, IL‐1A, Interleukin 1α, Interleukin-1 (genetics), Male, Middle Aged, Multiple System Atrophy (genetics), Multiple System Atrophy (immunology), Multiple system atrophy, Polymorphism, Polymorphism, Genetic (genetics), Promoter Regions, Genetic (genetics), Risk Factors, Risk factor, multiple system atrophy, polymorphism.
MESH :
- chemical , genetics : Interleukin-1.
- genetics : Multiple System Atrophy, Polymorphism, Genetic, Promoter Regions, Genetic.
- immunology : Multiple System Atrophy.
- Adult, Aged, Female, Genotype, Humans, Male, Middle Aged, Risk Factors.

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:

https://api.istex.fr/document/EA0122126C20CDFB90F8EF625D60F95ED90A83E1/fulltext/pdf

DOI: 10.1002/mds.10540

Affiliations:

Espagne

Le document en format XML

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<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>
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Movement Disorders (revue)

Interleukin‐1A (−889) genetic polymorphism increases the risk of multiple system atrophy

Interleukin‐1A (−889) genetic polymorphism increases the risk of multiple system atrophy

Source :

Descripteurs français

English descriptors

Abstract

Links toward previous steps (curation, corpus...)

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri

	Movement Disorders (revue)
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