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FAM167A gene

Known as: FAM167A, CHROMOSOME 8 OPEN READING FRAME 13, FAMILY WITH SEQUENCE SIMILARITY 167, MEMBER A 
National Institutes of Health

Related topics

Related topics

1 relation
C8orf4 gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
P014 FAM167A/BLK is a susceptibility locus in autoimmune diseases: characterisation of the FAM167 gene family
Introduction Genome-wide association studies of multiple autoimmune diseases, including Sjögren’s syndrome, systemic lupus… 
2018
2018
Clinical associations and expression pattern of the autoimmunity susceptibility factor DIORA-1 in patients with primary Sjögren’s syndrome
Sjogren’s syndrome (SS) is characterised by B cell abnormalities and immune-mediated destruction of exocrine glands, primarily… 
2018
2018
CD4+ and B lymphocyte expression quantitative traits at rheumatoid arthritis risk loci in untreated early arthritis: implications for causal gene identification
Objective Rheumatoid arthritis (RA) is a genetically complex disease of immune dysregulation. This study sought to gain further… 
2016
2016
Genetic risk of TNFSF4 and FAM167A-BLK polymorphisms in children with asthma and allergic rhinitis in a Han Chinese population
Abstract Background: Asthma and allergic rhinitis (AR) frequently occur as comorbid diseases of the upper airways. Single… 
2016
2016
Association of FAM 167 A-BLK rs 2736340 Polymorphism with Susceptibility to Autoimmune Diseases : A Meta-Analysis
Objective: The purpose of this study is to evaluate the correlation between family with sequence similarity 167A-B lymphoid… 
2014
2014
Possible Single-Nucleotide Polymorphism Loci Associated with Systemic Sclerosis Susceptibility: A Genetic Association Study in a Chinese Han Population
Objective The aim of this study was to confirm the association of RHOB and FAM167A-BLK gene polymorphisms with susceptibility to… 
2013
2013
Polymorphisms in the FAM167A-BLK, but not BANK1, are associated with primary Sjögren's syndrome in a Han Chinese population.
OBJECTIVES Primary Sjögren's syndrome (pSS) is an autoimmune disease with a complex genetic background. Single nucleotide… 
Review
2010
Review
2010
The genetics of systemic sclerosis.
Systemic sclerosis (SSc, scleroderma) is an autoimmune disease clinically characterized by progressive fibrosis in the skin and… 
2010
2010
Gene Variants In Fam167A-Blk And Tnfsf4 Are Associated With Primary Sjogren'S Syndrome
2010
2010
GENE VARIANTS IN FAM167A-BLK AND TNFSF4 ARE ASSOCIATED WITH PRIMARY SJOGRENS SYNDROME in SCANDINAVIAN JOURNAL OF RHEUMATOLOGY, vol 39, issue , pp 32-32
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