NQO1 gene rs1800566 variant is not associated with risk for multiple sclerosis. - Wikidata - awgldk - TriplyDB

NQO1 gene rs1800566 variant is not associated with risk for multiple sclerosis.

NQO1 gene rs1800566 variant is not associated with risk for multiple sclerosis.

http://www.wikidata.org/entity/Q33617100

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The GSTP1 gene variant rs1695 is not associated with an increased risk of multiple sclerosis Heme Oxygenase-1 and 2 Common Genetic Variants and Risk for Multiple Sclerosis.

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NQO1 gene rs1800566 variant is not associated with risk for multiple sclerosis.

http://www.wikidata.org/entity/Q33617100

description

2014 nî lūn-bûn

@nan

2014 թուականի Ապրիլին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի ապրիլին հրատարակված գիտական հոդված

@hy

2014年の論文

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2014年論文

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2014年論文

@zh-hant

2014年論文

@zh-hk

2014年論文

@zh-mo

2014年論文

@zh-tw

2014年论文

@wuu

name

NQO1 gene rs1800566 variant is not associated with risk for multiple sclerosis.

@ast

NQO1 gene rs1800566 variant is not associated with risk for multiple sclerosis.

@en

type

label

NQO1 gene rs1800566 variant is not associated with risk for multiple sclerosis.

@ast

NQO1 gene rs1800566 variant is not associated with risk for multiple sclerosis.

@en

prefLabel

NQO1 gene rs1800566 variant is not associated with risk for multiple sclerosis.

@ast

NQO1 gene rs1800566 variant is not associated with risk for multiple sclerosis.

@en

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1471-2377-14-87

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NQO1 gene rs1800566 variant is not associated with risk for multiple sclerosis.

@en

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Carmen Martínez

http://www.w3.org/2001/XMLSchema#string

Diana Pisa

http://www.w3.org/2001/XMLSchema#string

Dolores Torrecillas

http://www.w3.org/2001/XMLSchema#string

Félix Javier Jiménez-Jiménez

http://www.w3.org/2001/XMLSchema#string

Hortensia Alonso-Navarro

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Jorge Millán-Pascual

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José A G Agúndez

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José Francisco Plaza-Nieto

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Laura Turpín-Fenoll

http://www.w3.org/2001/XMLSchema#string

Lucía Ayuso-Peralta

http://www.w3.org/2001/XMLSchema#string

P2860

Recommended diagnostic criteria for multiple sclerosis: Guidelines from the international panel on the diagnosis of multiple sclerosis

Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis

Histamine-N-methyl transferase polymorphism and risk for multiple sclerosis

Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci.

Integrating mobile-phone based assessment for psychosis into people's everyday lives and clinical care: a qualitative study.

Accumulation of protein carbonyls within cerebellar astrocytes in murine experimental autoimmune encephalomyelitis.

Elevated protein carbonylation in the brain white matter and gray matter of patients with multiple sclerosis.

Increase of uric acid and purine compounds in biological fluids of multiple sclerosis patients.

LINGO1 rs9652490 and rs11856808 polymorphisms are not associated with risk for multiple sclerosis.

Decreased activity of the 20S proteasome in the brain white matter and gray matter of patients with multiple sclerosis.

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Elena García-Martín

Julián Benito-León

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