(Q52647916)

5 May 2018

title

Analysis of the association between Fc receptor family gene polymorphisms and ocular Behçet's disease in Han Chinese. (English)

1 reference

5 May 2018

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7

Aize Kijlstra

1 reference

5 May 2018

Donglei Zhang

1

1 reference

5 May 2018

Jieying Qin

2

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5 May 2018

Lin Li

3

1 reference

5 May 2018

Guannan Su

4

1 reference

5 May 2018

Guo Huang

5

1 reference

5 May 2018

Qingfeng Cao

6

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5 May 2018

Peizeng Yang

8

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5 May 2018

language of work or name

English

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publication date

19 March 2018

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5 May 2018

published in

Scientific Reports

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5 May 2018

volume

8

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5 May 2018

issue

1

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5 May 2018

page(s)

4850

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5 May 2018

Creative Commons Attribution 4.0 International

copyright license

start time

19 March 2018

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

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Targeted resequencing of candidate genes reveals novel variants associated with severe Behçet's uveitis

22 May 2018

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New insights into the pathogenesis of Behçet's disease

22 May 2018

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IgA and IgG antineutrophil cytoplasmic antibody engagement of Fc receptor genetic variants influences granulomatosis with polyangiitis

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Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behçet's disease

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Natural killer cells control a T-helper 1 response in patients with Behçet's disease

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Association between polymorphisms of FCRL3, a non-HLA gene, and Behçet's disease in a Chinese population with ophthalmic manifestations

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Treatment of retinal vasculitis in Behçet's disease with rituximab

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Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants

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Clinical features of chinese patients with Behçet's disease

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TH17 cells contribute to uveitis and scleritis and are expanded by IL-2 and inhibited by IL-27/STAT1.

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22 May 2018

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22 May 2018

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Chronic signs of memory B cell activation in patients with Behçet's disease are partially restored by anti-tumour necrosis factor treatment.

22 May 2018

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Two-stage association study in Chinese Han identifies two independent associations in CCR1/CCR3 locus as candidate for Behçet's disease susceptibility.

13 August 2018

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Imbalance of Th17 to Th1 cells in Behçet's disease.

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FcgammaRIIa, IIIa and IIIb gene polymorphisms in Behçet's disease: do they have any clinical implications?

13 August 2018

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The high producer variant of the Fc-receptor like-3 (FCRL3) gene is involved in protection against multiple sclerosis

13 August 2018

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Association analysis of functional variants of the FcgRIIa and FcgRIIIa genes with type 1 diabetes, celiac disease and rheumatoid arthritis.

13 August 2018

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CD8brightCD56+ T cells are cytotoxic effectors in patients with active Behcet's uveitis

13 August 2018

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Genetics of Behçet disease inside and outside the MHC

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7 January 2021

Association of FCRL4 polymorphisms on disease susceptibility and severity of ankylosing spondylitis in Chinese Han population

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7 January 2021

Associations between FCGR3A polymorphisms and susceptibility to rheumatoid arthritis: a metaanalysis

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7 January 2021

Genetic susceptibility and haplotype analysis between Fcgamma receptor IIB and IIIA gene with systemic lupus erythematosus in Chinese population

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7 January 2021

The number of CD8+ T cells and NKT cells increases in the aqueous humor of patients with Behçet's uveitis

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https://api.crossref.org/works/10.1038%2FS41598-018-23222-8

7 January 2021

Cytokine profile in Behçet's disease patients. Relationship with disease activity

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https://api.crossref.org/works/10.1038%2FS41598-018-23222-8

7 January 2021

Increased peripheral blood gamma delta+ T cells and natural killer cells in Behçet's disease

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12 December 2020

Criteria for diagnosis of Behçet's disease. International Study Group for Behçet's Disease

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12 December 2020

Serum levels of Th2 cytokines IL-4 and IL-10 in Behçet's disease

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12 December 2020

Behçet's disease: an update on the pathogenesis

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12 December 2020

10.1038/S41598-018-23222-8

Identifiers

DOI

1 reference

5 May 2018

PMCID

5859267

1 reference

5 May 2018

PubMed ID

29555961

1 reference

5 May 2018