Pages that link to "Q36802965"
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The following pages link to Is FCRL3 a new general autoimmunity gene? (Q36802965):
Displaying 37 items.
- Systemic lupus erythematosus features in rheumatoid arthritis and their effect on overall mortality (Q33381978) (← links)
- Expression of the autoimmune susceptibility gene FcRL3 on human regulatory T cells is associated with dysfunction and high levels of programmed cell death-1. (Q33951920) (← links)
- Human FcR polymorphism and disease (Q34406254) (← links)
- A refined study of FCRL genes from a genome-wide association study for Graves' disease (Q34625570) (← links)
- Replication of association of nine susceptibility loci with Graves' disease in the Chinese Han population (Q34770032) (← links)
- FCRL3 gene polymorphisms confer autoimmunity risk for allergic rhinitis in a Chinese Han population (Q34977535) (← links)
- CD4+FOXP3+ T regulatory cells in human autoimmunity: more than a numbers game (Q35178495) (← links)
- Association of Fc receptor-like 5 (FCRL5) with Graves' disease is secondary to the effect of FCRL3. (Q35822169) (← links)
- A functional variant in FCRL3 is associated with higher Fc receptor-like 3 expression on T cell subsets and rheumatoid arthritis disease activity. (Q36028278) (← links)
- Immunogenetics of autoimmune thyroid diseases: A comprehensive review (Q36236762) (← links)
- The Fc Receptor-Like 3 Polymorphisms (rs7528684, rs945635, rs3761959 and rs2282284) and The Risk of Neuromyelitis Optica in A Chinese Population (Q36255859) (← links)
- Genetic associations of FCRL3 polymorphisms with the susceptibility of Graves ophthalmopathy in a Chinese population (Q36318253) (← links)
- Cell damage and autoimmunity: a critical appraisal (Q36440448) (← links)
- Association between polymorphisms of FCRL3, a non-HLA gene, and Behçet's disease in a Chinese population with ophthalmic manifestations (Q36992630) (← links)
- Autoimmunity since the 1957 clonal selection theory: a little acorn to a large oak. (Q37015268) (← links)
- Polymorphisms of FCRL3 in a Chinese population with Vogt-Koyanagi-Harada (VKH) syndrome (Q37194571) (← links)
- Concordant and discordant associations between rheumatoid arthritis, systemic lupus erythematosus and ankylosing spondylitis based on all hospitalizations in Sweden between 1973 and 2004. (Q37324671) (← links)
- Association between Fc receptor-like 3 C169T polymorphism and risk of systemic lupus erythematosus: a meta-analysis. (Q37535675) (← links)
- Treg cells in rheumatoid arthritis: an update (Q38124277) (← links)
- Emerging roles for the FCRL family members in lymphocyte biology and disease (Q38239271) (← links)
- Four FCRL3 Gene Polymorphisms (FCRL3_3, _5, _6, _8) Confer Susceptibility to Multiple Sclerosis: Results from a Case-Control Study (Q39019331) (← links)
- FCRL3 promotes TLR9-induced B-cell activation and suppresses plasma cell differentiation (Q39125477) (← links)
- A genome-wide association study identifies two new risk loci for Graves' disease. (Q39671701) (← links)
- MHC2TA and FCRL3 genes are not associated with rheumatoid arthritis in Mexican patients. (Q41388881) (← links)
- Association of FCRL3 genotypes with susceptibility of Iranian patients to rheumatoid arthritis (Q43453423) (← links)
- Trisomy 21 causes changes in the circulating proteome indicative of chronic autoinflammation. (Q44645053) (← links)
- No significant association between Fc receptor-like 3 gene polymorphisms and human leukocyte antigen-B27 positive ankylosing spondylitis in Han Chinese population (Q46921963) (← links)
- Genomic determinants of long-term cardiometabolic complications in childhood acute lymphoblastic leukemia survivors (Q47098257) (← links)
- Coincidence of PTPN22 c.1858CC and FCRL3 -169CC genotypes as a biomarker of preserved residual β-cell function in children with type 1 diabetes. (Q48004863) (← links)
- FcRL3 gene promoter variant is associated with peripheral arthritis in Crohn's disease (Q51655067) (← links)
- Fc receptor-like 3 (FCRL3) -169 C/T polymorphism and systemic lupus erythematosus: a meta-analysis. (Q53116634) (← links)
- Three Case Reports of Rhupus Syndrome: An Overlap Syndrome of Rheumatoid Arthritis and Systemic Lupus Erythematosus. (Q55280876) (← links)
- Fc receptor-like 3 (-169T>C) polymorphism increases the risk of tendinopathy in volleyball athletes: a case control study (Q56667671) (← links)
- Association of FCRL4 polymorphisms on disease susceptibility and severity of ankylosing spondylitis in Chinese Han population (Q84552445) (← links)
- Single Nucleotide Polymorphisms of FCRL3 in Iranian Patients with Behcet's Disease (Q92158221) (← links)
- Genetic basis of rotator cuff injury: a systematic review (Q93059911) (← links)
- Two genetic variants explain the association of European ancestry with multiple sclerosis risk in African-Americans (Q100512373) (← links)