Genetic variation in the IL7RA/IL7 pathway increases multiple sclerosis susceptibility. - Wikidata - wikimedia - TriplyDB

Genetic variation in the IL7RA/IL7 pathway increases multiple sclerosis susceptibility.

Genetic variation in the IL7RA/IL7 pathway increases multiple sclerosis susceptibility.

http://www.wikidata.org/entity/Q33790356

about

Stage-specific immune dysregulation in multiple sclerosis The genetic basis of multiple sclerosis: a model for MS susceptibility.IL7Rα contributes to experimental autoimmune encephalomyelitis through altered T cell responses and nonhematopoietic cell lineages IL-7Rα confers susceptibility to experimental autoimmune encephalomyelitis.Genetic association of rs1520333 G/A polymorphism in the IL7 gene with multiple sclerosis susceptibility in Isfahan population.Fine mapping and functional analysis of the multiple sclerosis risk gene CD6 Body fluid biomarkers in multiple sclerosis: how far we have come and how they could affect the clinic now and in the future Interrogating the complex role of chromosome 16p13.13 in multiple sclerosis susceptibility: independent genetic signals in the CIITA-CLEC16A-SOCS1 gene complex IL17 Mediates Pelvic Pain in Experimental Autoimmune Prostatitis (EAP)Variants of Interleukin-7/Interleukin-7 Receptor Alpha are Associated with Both Neuromyelitis Optica and Multiple Sclerosis Among Chinese Han Population in Southeastern China Association study of four polymorphisms in the interleukin-7 receptor alpha gene with multiple sclerosis in Eastern Iran An integrated approach to design novel therapeutic interventions for demyelinating disorders Regulation of CD4+ T-cell polarization by suppressor of cytokine signalling proteins.Cytokine gene polymorphisms and human autoimmune disease in the era of genome-wide association studies IL-7: the global builder of the innate lymphoid network and beyond, one niche at a time.From Identification to Characterization of the Multiple Sclerosis Susceptibility Gene CLEC16A.Clinical biomarkers in multiple sclerosis.The L-coding region of the DA strain of Theiler's murine encephalomyelitis virus causes dysfunction and death of myelin-synthesizing cells.Regulation of suppressors of cytokine signaling as a therapeutic approach in autoimmune diseases, with an emphasis on multiple sclerosis.Tolerance of activated pathogenic CD4+ T cells by transcriptional targeting of dendritic cells.A cytokine gene screen uncovers SOCS1 as genetic risk factor for multiple sclerosis.IL7RA haplotype-associated alterations in cellular immune function and gene expression patterns in multiple sclerosis.Cytokine gene polymorphisms in multiple sclerosis: a meta-analysis of 45 studies including 7379 cases and 8131 controls.Age and Age-Related Diseases: Role of Inflammation Triggers and Cytokines.

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P2860

Genetic variation in the IL7RA/IL7 pathway increases multiple sclerosis susceptibility.

http://www.wikidata.org/entity/Q33790356

description

2010 nî lūn-bûn

@nan

2010 թուականի Յունուարին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի հունվարին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

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name

Genetic variation in the IL7RA/IL7 pathway increases multiple sclerosis susceptibility.

@ast

Genetic variation in the IL7RA/IL7 pathway increases multiple sclerosis susceptibility.

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type

label

Genetic variation in the IL7RA/IL7 pathway increases multiple sclerosis susceptibility.

@ast

Genetic variation in the IL7RA/IL7 pathway increases multiple sclerosis susceptibility.

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prefLabel

Genetic variation in the IL7RA/IL7 pathway increases multiple sclerosis susceptibility.

@ast

Genetic variation in the IL7RA/IL7 pathway increases multiple sclerosis susceptibility.

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Genetic variation in the IL7RA/IL7 pathway increases multiple sclerosis susceptibility.

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Cristin Aubin

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Denis Evans

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International Multiple Sclerosis Genetics Consortium

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Jacob L McCauley

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Jorge R Oksenberg

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Laura Piccio

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Neelum T Aggarwal

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Philip L De Jager

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Rebecca L Zuvich

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Stephen L Hauser

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P2860

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

A comprehensive review of genetic association studies

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

The expanding genetic overlap between multiple sclerosis and type I diabetes

Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci

Haploview: analysis and visualization of LD and haplotype maps

Genomic convergence: identifying candidate genes for Parkinson's disease by combining serial analysis of gene expression and genetic linkage

Signaling through the JAK/STAT pathway, recent advances and future challenges

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A genome screen in multiple sclerosis reveals susceptibility loci on chromosome 6p21 and 17q22

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5

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127

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Alastair Compston

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Margaret A. Pericak-Vance

Jonathan L Haines

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2010-01-30T00:00:00Z

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41175291

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1035939162

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20112030

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multiple sclerosis

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