(Q38060661)

28 August 2017

1 reference

title

The genetics of Behçet's disease in a Chinese population (English)

1 reference

28 August 2017

0 references

2

Aize Kijlstra

1 reference

28 August 2017

Shengping Hou

1

1 reference

28 August 2017

Peizeng Yang

series ordinal

3

1 reference

28 August 2017

publication date

15 November 2012

1 reference

28 August 2017

published in

Frontiers of medicine

1 reference

28 August 2017

volume

6

1 reference

28 August 2017

issue

4

1 reference

28 August 2017

page(s)

354-359

1 reference

Shared and distinct genetic variants in type 1 diabetes and celiac disease

28 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1007%2FS11684-012-0234-2

Current concepts in the etiology and treatment of Behçet disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11684-012-0234-2

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11684-012-0234-2

Clinical patterns and characteristics of uveitis in a tertiary center for uveitis in China.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11684-012-0234-2

Number VII Behçet's disease (Adamantiades syndrome).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11684-012-0234-2

Prevalence of Behçet's disease in Istanbul, Turkey.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11684-012-0234-2

Behçet's disease as an autoinflammatory disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11684-012-0234-2

SUMO4 gene polymorphisms in Chinese Han patients with Behcet's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11684-012-0234-2

HLA-B51/B5 and the risk of Behçet's disease: a systematic review and meta-analysis of case-control genetic association studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11684-012-0234-2

Ocular involvement is associated with HLA-B51 in Adamantiades-Behçet's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11684-012-0234-2

An insertion-deletion polymorphism in the interferon regulatory Factor 5 (IRF5) gene confers risk of inflammatory bowel diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11684-012-0234-2

Interferon regulatory factor 5 (IRF5) gene variants are associated with multiple sclerosis in three distinct populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11684-012-0234-2

No association of PTPN22 polymorphisms with susceptibility to ocular Behcet's disease in two Chinese Han populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11684-012-0234-2

The association of the PTPN22 620W polymorphism with Behcet's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11684-012-0234-2

No association of CTLA-4 polymorphisms with susceptibility to Behçet disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11684-012-0234-2

CTLA-4 polymorphisms are not associated with ocular inflammatory disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11684-012-0234-2

CTLA-4 +49A/G polymorphism is associated with Behçet's disease in a Tunisian population

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11684-012-0234-2

Common variants at CD40 and other loci confer risk of rheumatoid arthritis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11684-012-0234-2

PD-1 and its ligands in tolerance and immunity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11684-012-0234-2

Lack of an association of PD-1 and its ligand genes with Behcet's disease in a Chinese Han population

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11684-012-0234-2

A new haplotype of PDCD1 is associated with rheumatoid arthritis in Hong Kong Chinese.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11684-012-0234-2

A PD-1 polymorphism is associated with disease progression in multiple sclerosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11684-012-0234-2

A regulatory polymorphism in PDCD1 is associated with susceptibility to systemic lupus erythematosus in humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11684-012-0234-2

Role of Rho family GTPases in CCR1- and CCR5-induced actin reorganization in macrophages

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11684-012-0234-2

CCR1 chemokine receptor antagonist

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11684-012-0234-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11684-012-0234-2

STAT4 polymorphism in a Chinese Han population with Vogt-Koyanagi-Harada syndrome and Behçet's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11684-012-0234-2

Identification of a susceptibility locus in STAT4 for Behçet's disease in Han Chinese in a genome-wide association study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11684-012-0234-2

Behçet's disease exhibits an increased osteopontin serum level in active stage but no association with osteopontin and its receptor gene polymorphisms.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11684-012-0234-2

JAK2 and STAT3 polymorphisms in a Han Chinese population with Behçet's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11684-012-0234-2

Interleukin-17 gene polymorphism is associated with Vogt-Koyanagi-Harada syndrome but not with Behçet's disease in a Chinese Han population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11684-012-0234-2

Genome-wide association studies identify IL23R-IL12RB2 and IL10 as Behçet's disease susceptibility loci

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11684-012-0234-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11684-012-0234-2

Monocyte chemoattractant protein-1 -2518 A/G single nucleotide polymorphism in Chinese Han patients with ocular Behçet's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11684-012-0234-2

Association analysis of TGFBR3 gene with Vogt-Koyanagi-Harada disease and Behcet's disease in the Chinese Han population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11684-012-0234-2

Identification of novel genetic susceptibility loci for Behçet's disease using a genome-wide association study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11684-012-0234-2

Replication study confirms the association between UBAC2 and Behçet's disease in two independent Chinese sets of patients and controls

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11684-012-0234-2

A putative functional variant within the UBAC2 gene is associated with increased risk of Behçet's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11684-012-0234-2

SUMO4 C438T polymorphism is associated with papulopustular skin lesion in Korean patients with Behçet's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11684-012-0234-2

Interferon regulatory factor-5 is genetically associated with systemic lupus erythematosus in African Americans

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11684-012-0234-2

Analysis ofIRF5 gene functional polymorphisms in rheumatoid arthritis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11684-012-0234-2

Evidence for linkage of the HLA-B locus in Behçet's disease, obtained using the transmission disequilibrium test

21 January 2018

1 reference

12 December 2020

HLA-B*51 allele analysis by the PCR-SBT method and a strong association of HLA-B*5101 with Japanese patients with Behçet's disease

1 reference

12 December 2020

Association of small ubiquitin-like modifier 4 gene polymorphisms with rheumatoid arthritis in a Tunisian population.

1 reference

12 December 2020

Comparison of patients with Behçet's disease in the 1980s and 1990s

1 reference

12 December 2020

LPS induces eosinophil migration via CCR3 signaling through a mechanism independent of RANTES and Eotaxin

1 reference

12 December 2020

CD40 gene polymorphisms confer risk of Behcet's disease but not of Vogt-Koyanagi-Harada syndrome in a Han Chinese population

1 reference

12 December 2020

There is no association of CCR6 polymorphisms with susceptibility to Behcet's disease in two Chinese Han populations

1 reference

12 December 2020

The role of CD40-CD154 interaction in cell immunoregulation

1 reference

12 December 2020

IL-23R gene confers susceptibility to Behcet's disease in a Chinese Han population

1 reference

12 December 2020

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

1 reference

12 December 2020

Lack of association between CTLA-4 +49A/G and -318C/T polymorphisms and Behçet's disease risk: a meta-analysis

1 reference

12 December 2020

Lack of association of two polymorphisms of IRF5 with Behcet's disease

1 reference

12 December 2020

10.1007/S11684-012-0234-2

Identifiers

DOI

1 reference

Dimensions Publication ID

28 August 2017

1016697232

0 references

Fatcat ID

release_rqvq2nuhqfeynf7bhq54sec7ni

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/rqvq2nuhqfeynf7bhq54sec7ni

24 November 2022

mapped directly with Wikidata item

1 reference