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

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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