MAVS is not a Likely Susceptibility Locus for Addison's Disease and Type 1 Diabetes. - Wikidata - wikimedia - TriplyDB

MAVS is not a Likely Susceptibility Locus for Addison's Disease and Type 1 Diabetes.

MAVS is not a Likely Susceptibility Locus for Addison's Disease and Type 1 Diabetes.

http://www.wikidata.org/entity/Q33695036

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MAVS is not a Likely Susceptibility Locus for Addison's Disease and Type 1 Diabetes.

http://www.wikidata.org/entity/Q33695036

description

2016 nî lūn-bûn

@nan

2016 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

@hyw

2016 թվականի սեպտեմբերին հրատարակված գիտական հոդված

@hy

2016年の論文

@ja

2016年学术文章

@wuu

2016年学术文章

@zh-cn

2016年学术文章

@zh-hans

2016年学术文章

@zh-my

2016年学术文章

@zh-sg

2016年學術文章

@yue

name

MAVS is not a Likely Susceptibility Locus for Addison's Disease and Type 1 Diabetes.

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MAVS is not a Likely Susceptibility Locus for Addison's Disease and Type 1 Diabetes.

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type

label

MAVS is not a Likely Susceptibility Locus for Addison's Disease and Type 1 Diabetes.

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MAVS is not a Likely Susceptibility Locus for Addison's Disease and Type 1 Diabetes.

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prefLabel

MAVS is not a Likely Susceptibility Locus for Addison's Disease and Type 1 Diabetes.

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MAVS is not a Likely Susceptibility Locus for Addison's Disease and Type 1 Diabetes.

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Archivum Immunologiae et Therapiae Experimentalis

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MAVS is not a Likely Susceptibility Locus for Addison's Disease and Type 1 Diabetes.

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Grzegorz Przybylski

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Jerzy Nowak

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Marek Ruchala

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Marta Fichna

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Marta Kazimierska

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Piotr Fichna

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P2860

A large-scale replication study identifies TNIP1, PRDM1, JAZF1, UHRF1BP1 and IL10 as risk loci for systemic lupus erythematosus

Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes

A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1.

Mutations in DDX58, which encodes RIG-I, cause atypical Singleton-Merten syndrome.

Aicardi-Goutières syndrome is caused by IFIH1 mutations.

A specific IFIH1 gain-of-function mutation causes Singleton-Merten syndrome.

Copy Number Variation of TLR-7 Gene and its Association with the Development of Systemic Lupus Erythematosus in Female Patients from Yucatan Mexico.

A loss-of-function variant of the antiviral molecule MAVS is associated with a subset of systemic lupus patients.

Toll-like receptors, RIG-I-like RNA helicases and the antiviral innate immune response.

Intracellular pathogen detection by RIG-I-like receptors.

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271-274

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10.1007/S00005-016-0426-6

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3

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Agnieszka Dzikiewicz-Krawczyk

Magdalena Zurawek

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2016-09-20T00:00:00Z

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1005039927

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27652379

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type-1 diabetes

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