Cargando…

Genetic polymorphisms of C-type lectin receptors in Behcet’s disease in a Chinese Han population

C-type lectin receptors (CLRs) have been demonstrated to be involved in several autoimmune diseases. The role of CLRs in Behcet’s disease (BD) is unknown and thus was the purpose of this study. A two-stage association study was carried out and a total of 766 BD patients and 1674 healthy controls wer...

Descripción completa

Detalles Bibliográficos
Autores principales:	Yang, Yi, Tan, Handan, Deng, Bolin, Yu, Hongsong, Su, Guannan, Hu, Jiayue, Cao, Qingfeng, Yuan, Gangxiang, Kijlstra, Aize, Yang, Peizeng
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Nature Publishing Group UK 2017
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5509750/ https://www.ncbi.nlm.nih.gov/pubmed/28706259 http://dx.doi.org/10.1038/s41598-017-05877-x

Ejemplares similares

Genetic polymorphisms of cell adhesion molecules in Behcet’s disease in a Chinese Han population
por: Zheng, Minming, et al.
Publicado: (2016)

Functional Genetic Polymorphisms in the IL1RL1–IL18R1 Region Confer Risk for Ocular Behçet’s Disease in a Chinese Han Population
por: Tan, Xiao, et al.
Publicado: (2020)

The Association of Chemokine Gene Polymorphisms with VKH and Behcet's Disease in a Chinese Han Population
por: Huang, Yang, et al.
Publicado: (2017)

Association of a NOS3 gene polymorphism with Behçet’s disease but not with Vogt-Koyanagi-Harada syndrome in Han Chinese
por: Zhou, Yan, et al.
Publicado: (2016)

Association of LACC1, CEBPB-PTPN1, RIPK2 and ADO-EGR2 with ocular Behcet’s disease in a Chinese Han population
por: Wu, Pengcheng, et al.
Publicado: (2018)

Analysis of the association between Fc receptor family gene polymorphisms and ocular Behçet’s disease in Han Chinese
por: Zhang, Donglei, et al.
Publicado: (2018)

Genetic aspects of idiopathic paediatric uveitis and juvenile idiopathic arthritis associated uveitis in Chinese Han
por: Deng, Jing, et al.
Publicado: (2020)

Case-Control Study and Meta-Analysis Show a Weak Association between ANTXR2 Polymorphisms and Ankylosing Spondylitis in Chinese Han
por: Hu, Jiayue, et al.
Publicado: (2018)

Different Methylation of CpG-SNPs in Behcet's Disease
por: Huang, Yang, et al.
Publicado: (2019)

Changes in the Gut Microbiome Contribute to the Development of Behcet’s Disease via Adjuvant Effects
por: Wang, Qingfeng, et al.
Publicado: (2021)

Ocular Behcet’s disease is associated with aberrant methylation of interferon regulatory factor 8 (IRF8) in monocyte-derived dendritic cells
por: Qiu, Yiguo, et al.
Publicado: (2017)

Two Genetic Variations in the IRF8 region are associated with Behçet’s disease in Han Chinese
por: Jiang, Yanni, et al.
Publicado: (2016)

Genetic Variations of NLR family genes in Behcet’s Disease
por: Li, Lin, et al.
Publicado: (2016)

Analysis of receptor tyrosine kinase genetics identifies two novel risk loci in GAS6 and PROS1 in Behçet’s disease
por: Qin, Jieying, et al.
Publicado: (2016)

Corrigendum: Genetic Variations of NLR family genes in Behcet’s Disease
por: Li, Lin, et al.
Publicado: (2016)

Genetic analysis of innate immunity in Behcet’s disease identifies an association with IL-37 and IL-18RAP
por: Tan, Handan, et al.
Publicado: (2016)

No Association of PTPN22 Polymorphisms with Susceptibility to Ocular Behcet's Disease in Two Chinese Han Populations
por: Zhang, Qi, et al.
Publicado: (2012)

Association of a TNIP1 Polymorphism with Vogt-Koyanagi-Harada Syndrome but Not with Ocular Behcet’s Disease in Han Chinese
por: Shi, Yanyun, et al.
Publicado: (2014)

Lack of an Association of PD-1 and Its Ligand Genes with Behcet's Disease in a Chinese Han Population
por: Meng, Qianli, et al.
Publicado: (2011)

Interleukin-10 gene polymorphisms are associated with Behcet’s disease but not with Vogt-Koyanagi-Harada syndrome in the Chinese Han population
por: Hu, Jianmin, et al.
Publicado: (2015)

The haplotypes of various TNF related genes associated with scleritis in Chinese Han
por: Gao, Yingnan, et al.
Publicado: (2020)

Hypermethylation of Interferon Regulatory Factor 8 (IRF8) Confers Risk to Vogt-Koyanagi-Harada Disease
por: Qiu, Yiguo, et al.
Publicado: (2017)

Lack of association of miR-146a and Ets-1 gene polymorphisms with Fuchs uveitis syndrome in Chinese Han patients
por: Zhou, Qingyun, et al.
Publicado: (2012)

Metabolomic Analysis of Aqueous Humor Identifies Aberrant Amino Acid and Fatty Acid Metabolism in Vogt-Koyanagi-Harada and Behcet’s Disease
por: Xu, Jing, et al.
Publicado: (2021)

CD40 polymorphisms in Han Chinese patients with Fuch uveitis syndrome
por: Chen, Feilan, et al.
Publicado: (2011)

Decreased B and T lymphocyte attenuator in Behcet’s disease may trigger abnormal Th17 and Th1 immune responses
por: Ye, Zi, et al.
Publicado: (2016)

Association between polymorphisms of FCRL3, a non-HLA gene, and Behçet’s disease in a Chinese population with ophthalmic manifestations
por: Li, Ke, et al.
Publicado: (2008)

Aberrant DNA methylation of GATA binding protein 3 (GATA3), interleukin-4 (IL-4), and transforming growth factor-β (TGF-β) promoters in Behcet's disease
por: Zhu, Yunyun, et al.
Publicado: (2017)

TNFAIP3 Gene Polymorphisms in a Chinese Han Population with Vogt–Koyanagi–Harada Syndrome
por: Li, Hong, et al.
Publicado: (2013)

FGFR1OP tagSNP but Not CCR6 Polymorphisms Are Associated with Vogt-Koyanagi-Harada Syndrome in Chinese Han
por: Yi, Xianglong, et al.
Publicado: (2013)

Copy Number Variants and Genetic Polymorphisms in TBX21, GATA3, Rorc, Foxp3 and Susceptibility to Behcet's Disease and Vogt-Koyanagi-Harada Syndrome
por: Liao, Dan, et al.
Publicado: (2015)

Copy number variations and gene polymorphisms of Complement components in ocular Behcet’s disease and Vogt-Koyanagi-Harada syndrome
por: Xu, Dengfeng, et al.
Publicado: (2015)

Small ubiquitin-like modifier 4 (SUMO4) polymorphisms and Vogt-Koyanagi-Harada (VKH) syndrome in the Chinese Han population
por: Hou, Shengping, et al.
Publicado: (2008)

Decreased Expression of the Aryl Hydrocarbon Receptor in Ocular Behcet's Disease
por: Wang, Chaokui, et al.
Publicado: (2014)

High Ambient Temperature Aggravates Experimental Autoimmune Uveitis Symptoms
por: Pan, Su, et al.
Publicado: (2021)

Genetic Variations of IL-12B, IL-12Rβ1, IL-12Rβ2 in Behcet's Disease and VKH Syndrome
por: Li, Xinyu, et al.
Publicado: (2014)

Increased Complement 3a Receptor is Associated with Behcet’s disease and Vogt-Koyanagi-Harada disease
por: Wang, Chaokui, et al.
Publicado: (2017)

Association of TNFSF4 Polymorphisms with Vogt-Koyanagi-Harada and Behcet’s Disease in Han Chinese
por: Lu, Sha, et al.
Publicado: (2016)

Decreased interleukin 27 expression is associated with active uveitis in Behçet’s disease
por: Wang, Chaokui, et al.
Publicado: (2014)

Replication study confirms the association between UBAC2 and Behçet's disease in two independent Chinese sets of patients and controls
por: Hou, Shengping, et al.
Publicado: (2012)

Cannot write session to /tmp/vufind_sessions/sess_6ucpl686hk9hj3ek1990cvjpr4