Association between copy number variation of complement component C4 and Graves' disease - Wikidata - wikimedia - TriplyDB

Association between copy number variation of complement component C4 and Graves' disease

Association between copy number variation of complement component C4 and Graves' disease

http://www.wikidata.org/entity/Q35540370

about

Early Components of the Complement Classical Activation Pathway in Human Systemic Autoimmune Diseases Dual effect of a polymorphism in the macrophage migration inhibitory factor gene is associated with new-onset Graves disease in a Taiwanese Chinese population.Association of IL12B polymorphisms with susceptibility to Graves ophthalmopathy in a Taiwan Chinese population.Copy number variations exploration of multiple genes in Graves' disease.Association between C4, C4A, and C4B copy number variations and susceptibility to autoimmune diseases: a meta-analysis.The complement system: a gateway to gene-environment interactions in schizophrenia pathogenesis.Copy number variations of complement component C4 are associated with Behçet's disease but not with ankylosing spondylitis associated with acute anterior uveitis.High C4 gene copy numbers protects against Vogt-Koyanagi-Harada syndrome in Chinese Han.

P2860

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P2860

Association between copy number variation of complement component C4 and Graves' disease

http://www.wikidata.org/entity/Q35540370

description

2011 nî lūn-bûn

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2011 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

@hyw

2011 թվականի սեպտեմբերին հրատարակված գիտական հոդված

@hy

2011年の論文

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2011年論文

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2011年論文

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2011年論文

@zh-hk

2011年論文

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2011年論文

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2011年论文

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name

Association between copy number variation of complement component C4 and Graves' disease

@ast

Association between copy number variation of complement component C4 and Graves' disease

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type

label

Association between copy number variation of complement component C4 and Graves' disease

@ast

Association between copy number variation of complement component C4 and Graves' disease

@en

prefLabel

Association between copy number variation of complement component C4 and Graves' disease

@ast

Association between copy number variation of complement component C4 and Graves' disease

@en

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Journal of Biomedical Science

P1476

Association between copy number variation of complement component C4 and Graves' disease

@en

P2093

Chang-Hai Tsai

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

Chwen-Tzuei Chang

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

Fuu-Jen Tsai

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

Lei Wan

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

Wen-Chi Chen

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

Wen-Ling Liao

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

Yu-Huei Liu

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

Yuhsin Tsai

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

P2860

Real-time PCR quantification of human complement C4A and C4B genes.

Genome-wide association study for vitiligo identifies susceptibility loci at 6q27 and the MHC

Copy number variation in the human genome and its implication in autoimmunity.

Disease association of the CD103 polymorphisms in Taiwan Chinese Graves' ophthalmopathy patients.

Genome-wide analysis identifies a quantitative trait locus in the MHC class II region associated with generalized vitiligo age of onset

Gene copy-number variation and associated polymorphisms of complement component C4 in human systemic lupus erythematosus (SLE): low copy number is a risk factor for and high copy number is a protective factor against SLE susceptibility in European A

Sex, MHC and complement C4 in autoimmune diseases.

The role of complement in inflammatory diseases from behind the scenes into the spotlight

The role of complement in autoimmune renal disease.

The etiology of autoimmune thyroid disease: a story of genes and environment

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18

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