Cargando…

A metagenomic study of the gut microbiome in Behcet’s disease

BACKGROUND: Behcet’s disease (BD) is a recalcitrant, multisystemic inflammatory disease that can lead to irreversible blindness. Microbial agents have been considered to contribute to the pathogenesis of this disease, but the underlying mechanisms remain unclear. In this study, we investigated the a...

Descripción completa

Detalles Bibliográficos
Autores principales:	Ye, Zi, Zhang, Ni, Wu, Chunyan, Zhang, Xinyuan, Wang, Qingfeng, Huang, Xinyue, Du, Liping, Cao, Qingfeng, Tang, Jihong, Zhou, Chunjiang, Hou, Shengping, He, Yue, Xu, Qian, Xiong, Xiao, Kijlstra, Aize, Qin, Nan, Yang, Peizeng
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2018
Materias:	Research
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6091101/ https://www.ncbi.nlm.nih.gov/pubmed/30077182 http://dx.doi.org/10.1186/s40168-018-0520-6

Ejemplares similares

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

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)

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

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)

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)

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)

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

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)

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)

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)

miR-23a, miR-146a and miR-301a confer predisposition to Vogt-Koyanagi-Harada syndrome but not to Behcet’s disease
por: Hou, Shengping, et al.
Publicado: (2016)

Increased Expression of IL-22 Is Associated with Disease Activity in Behcet’s Disease
por: Cai, Tao, et al.
Publicado: (2013)

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

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)

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

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

UVEOGENE: An SNP database for investigations on genetic factors associated with uveitis and their relationship with other systemic autoimmune diseases
por: Wang, Qingfeng, et al.
Publicado: (2019)

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)

A Functional Variant of PTPN22 Confers Risk for Vogt-Koyanagi-Harada Syndrome but Not for Ankylosing Spondylitis
por: Zhang, Qi, et al.
Publicado: (2014)

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)

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)

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

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)

Genetic polymorphisms of C-type lectin receptors in Behcet’s disease in a Chinese Han population
por: Yang, Yi, et al.
Publicado: (2017)

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)

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

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)

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

TRAF5 and TRAF3IP2 Gene Polymorphisms Are Associated with Behçet's Disease and Vogt-Koyanagi-Harada Syndrome: A Case-Control Study
por: Xiang, Qin, 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)

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

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

Label-Free Proteomics Reveals Decreased Expression of CD18 and AKNA in Peripheral CD4(+) T Cells from Patients with Vogt-Koyanagi-Harada Syndrome
por: Mao, Liming, et al.
Publicado: (2011)

Correction: Label-Free Proteomics Reveals Decreased Expression of CD18 and AKNA in Peripheral CD4(+) T Cells from Patients with Vogt-Koyanagi-Harada Syndrome
por: Mao, Liming, et al.
Publicado: (2011)

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

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)

PDCD1 genes may protect against extraocular manifestations in Chinese Han patients with Vogt-Koyanagi-Harada syndrome
por: Meng, Qianli, et al.
Publicado: (2009)

Polymorphisms of FCRL3 in a Chinese population with Vogt-Koyanagi-Harada (VKH) syndrome
por: Li, Ke, et al.
Publicado: (2009)

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

Development of revised diagnostic criteria for Fuchs’ uveitis syndrome in a Chinese population
por: Yang, Peizeng, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_n84g3893cle125kfh4n4voicfv