Fc-Gamma Receptor 3B Copy Number Variation Is Not a Risk Factor for Behçet's Disease. (Q36014406)

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5 February 2020

title

Fc-Gamma Receptor 3B Copy Number Variation Is Not a Risk Factor for Behçet's Disease (English)

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1

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Keyvan Saeedfar

7

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Fereydoun Davatchi

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author name string

Sue Lester

2

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Emma Dunstan

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Farhad Shahram

4

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Abdolhadi Nadji

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Noushin Bayat

6

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Naghmeh Ziaei

8

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Catherine Hill

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Maureen Rischmueller

10

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publication date

30 May 2012

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International journal of rheumatology

5 February 2020

published in

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volume

2012

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page(s)

167096

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Creative Commons Attribution 3.0 Unported

5 February 2020

copyright license

start time

1 January 2012

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April 2022 Public Data File from Crossref

copyright status

copyrighted

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April 2022 Public Data File from Crossref

cites work

Low copy number of the FCGR3B gene and rheumatoid arthritis: a case-control study and meta-analysis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3369435

Genome-wide association study identifies FCGR2A as a susceptibility locus for Kawasaki disease

2 October 2017

1 reference

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Etiopathogenesis of Behçet's disease with emphasis on the role of immunological aberrations

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3369435

Association of variation in Fcgamma receptor 3B gene copy number with rheumatoid arthritis in Caucasian samples

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3369435

FcgammaRIIB, FcgammaRIIIB, and systemic lupus erythematosus.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3369435

Structural variation in the human genome and its role in disease

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3369435

Copy number of FCGR3B, which is associated with systemic lupus erythematosus, correlates with protein expression and immune complex uptake

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3369435

Fcgamma receptors as regulators of immune responses

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3369435

FCGR3B copy number variation is associated with susceptibility to systemic, but not organ-specific, autoimmunity

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3369435

A proposed classification of the immunological diseases

2 October 2017

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2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3369435

Association of copy number variation in the FCGR3B gene with risk of autoimmune diseases

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3369435

Association of FCGR2A and FCGR2A-FCGR3A haplotypes with susceptibility to giant cell arteritis

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3369435

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

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3369435

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

23 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22701122

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1155/2012/167096

1 reference

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5 February 2020

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5 February 2020

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