Low copy number (CN) of the FCGR3B gene reduces FCGR3B membrane expression on neutrophils and results in clearance of a smaller amount of immune complex. We investigated FCGR3B CN in relation to the clinical phenotype in a Caucasian SLE cohort (n = 107). FCGR3B CN was determined by three different qPCR parameter estimations (Ct-, Cy0, and cpD1) and confirmed by the FCGR2C/FCGR2A paralog ratio test. Clinical and serological data were then analyzed for their association with FCGR3B CN. Low FCGR3B CN (2). In multivariate analyses, LN was independently associated with anti-C1q-Ab levels (P = 0.03) and low FCGR3B CN (P = 0.09). We conclude that the susceptibility for LN in patients with low FCGR3B CN is linked to increased levels of pathogenic a...
Introduction: Low copy number (CN) of the Fc gamma receptor 3B (FCGR3B) gene has been associated wit...
Introduction: Low copy number (CN) of the Fc gamma receptor 3B (FCGR3B) gene has been associated wit...
The Fcγ RIIIA-F158 allele is a risk factor for the development of lupus nephritis: A meta-analysis.B...
Low copy number (CN) of the FCGR3B gene reduces FCGR3B membrane expression on neutrophils and result...
Copy number (CN) variation (CNV) has been shown to be common in regions of the genome coding for imm...
Copy number (CN) variation (CNV) has been shown to be common in regions of the genome coding for imm...
Copy number (CN) variation (CNV) has been shown to be common in regions of the genome coding for imm...
Low-affinity Fc receptors (FcR) act as key mediators of the pathogenic effects of autoantibodies. In...
Copy number variation (CNV) is common in genomic regions encoding immune-related genes and can impac...
Antibodies to C1q in systemic lupus erythematosus: Characteristics and relation to FcγRIIA alleles. ...
Reduced FCGR3B copy number is associated with increased risk of systemic lupus erythematosus (SLE). ...
The Fcgamma-receptor locus on chromosome 1q23 shows copy-number variation (CNV), and it has previous...
There is increasing evidence that gene copy number (CN) variation influences clinical phenotype. The...
There is increasing evidence that gene copy number (CN) variation influences clinical phenotype. The...
Item does not contain fulltextThere is increasing evidence that gene copy number (CN) variation infl...
Introduction: Low copy number (CN) of the Fc gamma receptor 3B (FCGR3B) gene has been associated wit...
Introduction: Low copy number (CN) of the Fc gamma receptor 3B (FCGR3B) gene has been associated wit...
The Fcγ RIIIA-F158 allele is a risk factor for the development of lupus nephritis: A meta-analysis.B...
Low copy number (CN) of the FCGR3B gene reduces FCGR3B membrane expression on neutrophils and result...
Copy number (CN) variation (CNV) has been shown to be common in regions of the genome coding for imm...
Copy number (CN) variation (CNV) has been shown to be common in regions of the genome coding for imm...
Copy number (CN) variation (CNV) has been shown to be common in regions of the genome coding for imm...
Low-affinity Fc receptors (FcR) act as key mediators of the pathogenic effects of autoantibodies. In...
Copy number variation (CNV) is common in genomic regions encoding immune-related genes and can impac...
Antibodies to C1q in systemic lupus erythematosus: Characteristics and relation to FcγRIIA alleles. ...
Reduced FCGR3B copy number is associated with increased risk of systemic lupus erythematosus (SLE). ...
The Fcgamma-receptor locus on chromosome 1q23 shows copy-number variation (CNV), and it has previous...
There is increasing evidence that gene copy number (CN) variation influences clinical phenotype. The...
There is increasing evidence that gene copy number (CN) variation influences clinical phenotype. The...
Item does not contain fulltextThere is increasing evidence that gene copy number (CN) variation infl...
Introduction: Low copy number (CN) of the Fc gamma receptor 3B (FCGR3B) gene has been associated wit...
Introduction: Low copy number (CN) of the Fc gamma receptor 3B (FCGR3B) gene has been associated wit...
The Fcγ RIIIA-F158 allele is a risk factor for the development of lupus nephritis: A meta-analysis.B...