(Q53443485)

14 May 2018

title

FAS Gene Copy Numbers are Associated with Susceptibility to Behçet Disease and VKH Syndrome in Han Chinese. (English)

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14 May 2018

0 references

1

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14 May 2018

Qingfeng Cao

8

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14 May 2018

Aize Kijlstra

9

object named as

Aize Kijlstra

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14 May 2018

Le Luo

2

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14 May 2018

Lili Wu

3

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14 May 2018

Minming Zheng

4

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14 May 2018

Lijun Zhang

5

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14 May 2018

Yunjia Liu

6

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14 May 2018

Hua Li

7

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14 May 2018

Peizeng Yang

10

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14 May 2018

publication date

3 August 2015

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14 May 2018

published in

Human Mutation

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14 May 2018

volume

36

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14 May 2018

issue

11

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14 May 2018

page(s)

1064-1069

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14 May 2018

Copy number polymorphism in Fcgr3 predisposes to glomerulonephritis in rats and humans

cites work

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22829

Fas (CD95) and bcl-2 expression in active skin lesions of Behçet's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22829

Correlating multiallelic copy number polymorphisms with disease susceptibility

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22829

Association of FCGR3A and FCGR3B copy number variations with systemic lupus erythematosus and rheumatoid arthritis in Taiwanese patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22829

Structural variants: changing the landscape of chromosomes and design of disease studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22829

Human gene copy number variation and infectious disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22829

High C4 gene copy numbers protects against Vogt-Koyanagi-Harada syndrome in Chinese Han.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22829

Copy number variations of complement component C4 are associated with Behçet's disease but not with ankylosing spondylitis associated with acute anterior uveitis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22829

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/10.1002%2FHUMU.22829

Genetic association analysis of copy-number variation (CNV) in human disease pathogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22829

Epidemiology of Behçet disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22829

A functional copy-number variation in MAPKAPK2 predicts risk and prognosis of lung cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22829

Copy-number variation and association studies of human disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22829

Apoptosis in the pathogenesis of systemic lupus erythematosus.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22829

Revised diagnostic criteria for Vogt-Koyanagi-Harada disease: report of an international committee on nomenclature

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22829

Global variation in copy number in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22829

Confirmation of association of FCGR3B but not FCGR3A copy number with susceptibility to autoantibody positive rheumatoid arthritis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22829

Targeting immune privilege to prevent pathogenic neovascularization

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22829

Relative impact of nucleotide and copy number variation on gene expression phenotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22829

The possible impact of uveitis in blindness: a literature survey

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22829

A gender-specific association of CNV at 6p21.3 with NPC susceptibility

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22829

The Fas signaling pathway: more than a paradigm

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22829

A high copy number of FCGR3B is associated with psoriasis vulgaris in Han Chinese.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22829

Clinical features of chinese patients with Behçet's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22829

Clinical characteristics of Vogt-Koyanagi-Harada syndrome in Chinese patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22829

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22829

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22829

Relation of the Fas and FasL gene polymorphisms with susceptibility to and severity of rheumatoid arthritis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22829

Predisposition to Behçet's disease and VKH syndrome by genetic variants of miR-182.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22829

BCL-2 (-938C > A) polymorphism is associated with breast cancer susceptibility.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22829

Age-dependent changes in FasL (CD95L) modulate macrophage function in a model of age-related macular degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22829

FAS -670A>G promoter polymorphism is associated with soluble Fas levels in primary Sjögren’s syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22829

Functional polymorphisms of the FAS/FASLG genes are associated with risk of alopecia areata in a Chinese population: a case-control analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22829

7 January 2021

Genome-wide association analysis of Vogt-Koyanagi-Harada syndrome identifies two new susceptibility loci at 1p31.2 and 10q21.3.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22829

7 January 2021

Apoptosis and autoimmune diseases

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22829

7 January 2021

A six-nucleotide insertion-deletion polymorphism in the CASP8 promoter is associated with susceptibility to multiple cancers

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22829

7 January 2021

Aberrant Fas ligand expression in lymphocytes in patients with Behçet's disease

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22829

7 January 2021

A functional copy number variation in the WWOX gene is associated with lung cancer risk in Chinese

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22829

7 January 2021

Disturbed expression of Fas/FasL on CD4(+) and CD8(+)T cells in Behcet's disease, Vogt-Koyanagi-Harada syndrome, and idiopathic anterior uveitis

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22829

7 January 2021

Copy number variations of interleukin-17F, interleukin-21, and interleukin-22 are associated with systemic lupus erythematosus

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22829

7 January 2021

Identifiers

DOI

10.1002/HUMU.22829

1 reference

14 May 2018

PubMed ID

26136352

1 reference

14 May 2018