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FCRL3 encodes a member of the immunoglobulin receptor superfamily and is one of several Fc receptor-like glycoproteins clustered on the long arm of chromosome 1. Zusätzlich bieten wir Ihnen Fc Receptor-Like 3 Antikörper (19) und Fc Receptor-Like 3 Kits (2) und viele weitere Produktgruppen zu diesem Protein an.
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Pooled genome wide association study identified a genetic variant upstream of FCRL3 as a susceptibility locus for Graves' disease in addition to those identified in the Major Histo-compatibility Complex.
The expression of Sezary signature genes: FCRL3, Tox (zeige TOX Proteine), and miR (zeige MLXIP Proteine)-214, was significantly higher in samples from Sezary syndrome patients with CD164 (zeige CD164 Proteine) expressing CD4 (zeige CD4 Proteine)(+) T cells.
This study aims to investigate the association between common polymorphisms of FCRL3 gene and multiple sclerosis risk in a Chinese Han population.
Observed no association between the MHC2TA (zeige CIITA Proteine) or FCRL3 SNPs and rheumatoid arthritis in Mexican patients.
genetic polymorphism is associated with rheumatoid arthritis in Chinese Han population
Genetic polymorphisms in FCRL3 are genetic risk factors for neuromyelitis optica in the Chinese population.
CTLA4 (zeige CTLA4 Proteine) and FCRL3 genes overexpression may play an important role in children suffering from autoimmune thyroiditis.
FCRL3 genetic polymorphisms were associated with an increased risk of endometriosis-related infertility, regardless of symptoms.
4 Single Nucleotide Polymorphisms (rs7528684, rs945635, rs3761959, and rs2282284) could significantly elevate the risk of Neuromyelitis Optica in Chinese Han population.
study found a significant association between the SNPs in FCRL3 gene and allergic rhinitis (AR) in Chinese Han patients; results suggest these gene polymorphisms might be the autoimmunity risk for AR
FCRL5 (zeige FCRL5 Proteine) exerts binary and compartment-specific influence on innate-like B-cell receptor signaling.
The three amino-terminal immunoglobulin domains of FCRL5 (zeige FCRL5 Proteine) are required for binding of orthopoxvirus histocompatibility class I-like protein to B (zeige TDO2 Proteine) cells and monocytes/macrophages.
Fc receptor-like 5 inhibits B cell activation via SHP-1 tyrosine phosphatase recruitment.
This gene encodes a member of the immunoglobulin receptor superfamily and is one of several Fc receptor-like glycoproteins clustered on the long arm of chromosome 1. The encoded protein contains immunoreceptor-tyrosine activation motifs and immunoreceptor-tyrosine inhibitory motifs in its cytoplasmic domain and may play a role in regulation of the immune system. Mutations in this gene have been associated with rheumatoid arthritis, autoimmune thyroid disease, and systemic lupus erythematosus.
Fc receptor-like 3
, type I TM-receptor XFL1.2a
, type I TM-receptor XFL1.2b
, Fc receptor-like protein 3-like
, Fc receptor homolog 3
, Fc receptor-like protein 3
, IFGP family protein 3
, SH2 domain-containing phosphatase anchor protein 2
, fcR-like protein 3
, immune receptor translocation-associated protein 3
, immunoglobulin superfamily receptor translocation associated protein 3
, BXMAS1-like protein 2
, Fc receptor-like protein 5
, fc receptor homolog 3
, fcR-like protein 5