Integrated analyses of single-cell transcriptome and Mendelian randomization reveal the protective role of FCRL3 in multiple sclerosis. | Integrated analyses of single-cell transcriptome and Mendelian randomization reveal the protective role of FCRL3 in multiple sclerosis. Yu K, Jiang R, Li Z, Ren X, Jiang H, Zhao Z., Free PMC Article | 07/31/2024 |
FCRL3 expression is upregulated and closely correlates with TIGIT expression in regulatory T cells of patients with systemic lupus erythematosus. | FCRL3 expression is upregulated and closely correlates with TIGIT expression in regulatory T cells of patients with systemic lupus erythematosus. Bahabayi A, Zhang YH, Yuan Z, Wang Y, Zhang Z, Zeng X, Guan Z, Wang P, Liu C. | 05/28/2024 |
No evidence for a direct extracellular interaction between human Fc receptor-like 3 (MAIA) and the sperm ligand IZUMO1. | No evidence for a direct extracellular interaction between human Fc receptor-like 3 (MAIA) and the sperm ligand IZUMO1. Bianchi E, Jiménez-Movilla M, Cots-Rodríguez P, Viola C, Wright GJ., Free PMC Article | 02/26/2024 |
Single nucleotide polymorphisms of Interleukin - 4, Interleukin-18, FCRL3 and sPLA2IIa genes and their association in pathogenesis of endometriosis. | Single nucleotide polymorphisms of Interleukin - 4, Interleukin-18, FCRL3 and sPLA2IIa genes and their association in pathogenesis of endometriosis. Balunathan N, Rani G U, Perumal V, Kumarasamy P. | 05/4/2023 |
FCRL3 promotes IL-10 expression in B cells through the SHP-1 and p38 MAPK signaling pathways. | FCRL3 promotes IL-10 expression in B cells through the SHP-1 and p38 MAPK signaling pathways. Cui X, Liu CM, Liu QB. | 06/26/2021 |
Expression profile of Fc receptor-like molecules in patients with IgA nephropathy. | Expression profile of Fc receptor-like molecules in patients with IgA nephropathy. Zhong Z, Shi D, Xiao M, Fu D, Feng S, Kong Q, Li J, Li Z. | 04/3/2021 |
Human Fc Receptor-like 3 Inhibits Regulatory T Cell Function and Binds Secretory IgA. | Human Fc Receptor-like 3 Inhibits Regulatory T Cell Function and Binds Secretory IgA. Agarwal S, Kraus Z, Dement-Brown J, Alabi O, Starost K, Tolnay M. | 03/20/2021 |
Three SNPs of FCRL3 and one SNP of MTMR3 are associated with immunoglobulin A nephropathy risk. | Three SNPs of FCRL3 and one SNP of MTMR3 are associated with immunoglobulin A nephropathy risk. Zhang H, He Y, He X, Wang L, Jin T, Yuan D. | 01/9/2021 |
The results indicate that FCRL3 gene polymorphisms are associated with the development and progression of IgA nephropathy (IgAN) in a Chinese Han population, and the rs11264794-A allele showed a protective role for IgAN due to reduced specific binding between miR-183-5p.1 and FCRL3 3'-untranslated region. | Association of FCRL3 Gene Polymorphisms with IgA Nephropathy in a Chinese Han Population. Zhong Z, Feng S, Shi D, Xu R, Yin P, Wang M, Mao H, Huang F, Li Z, Yu X, Li M. | 10/19/2019 |
This study identified novel single nucleotide polymorphism in FCRL3 and FCRL5 significantly associated with the risk for asthma with comorbid allergic rhinitis in the Chinese population | Genetic risk of FCRL3 and FCRL5 polymorphisms in children with asthma and allergic rhinitis in a Chinese Han population. Gu Z, Shen Y, Tang XY, Ke X, Yao HB, Hong SL, Kang HY. | 05/11/2019 |
FCRL3 -169C allele may increase the risk of developing tendinopathy. | Fc receptor-like 3 (-169T>C) polymorphism increases the risk of tendinopathy in volleyball athletes: a case control study. Salles JI, Lopes LR, Duarte MEL, Morrissey D, Martins MB, Machado DE, Guimarães JAM, Perini JA., Free PMC Article | 04/20/2019 |
no association between the FCRL-3 rs7528684 SNP with susceptibility to allergic asthma in Iranian North-Western Azeri population. | Investigation of Fc Receptor-Like 3 (FCRL-3) Gene Polymorphism (rs7528684) with Susceptibility to Allergic Asthma in Iranian North-Western Azeri Population. Aslanian-Kalkhoran L, Elieh-Ali-Komi D, Sadeghi-Shabestari M, Shanebandi D, Babaloo Z, Razavi A, Sadigh-Eteghad S, Kazemi T. | 08/25/2018 |
-169CC genotype associated with a beneficial functional effect on residual insulin secretion and HbA1c level dynamics in type 1 diabetes | Coincidence of PTPN22 c.1858CC and FCRL3 -169CC genotypes as a biomarker of preserved residual β-cell function in children with type 1 diabetes. Pawłowicz M, Filipów R, Krzykowski G, Stanisławska-Sachadyn A, Morzuch L, Kulczycka J, Balcerska A, Limon J. | 07/14/2018 |
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. | Pooled genome wide association detects association upstream of FCRL3 with Graves' disease. Khong JJ, Burdon KP, Lu Y, Laurie K, Leonardos L, Baird PN, Sahebjada S, Walsh JP, Gajdatsy A, Ebeling PR, Hamblin PS, Wong R, Forehan SP, Fourlanos S, Roberts AP, Doogue M, Selva D, Montgomery GW, Macgregor S, Craig JE., Free PMC Article | 08/19/2017 |
The expression of Sezary signature genes: FCRL3, Tox, and miR-214, was significantly higher in samples from Sezary syndrome patients with CD164 expressing CD4(+) T cells. | CD164 identifies CD4(+) T cells highly expressing genes associated with malignancy in Sézary syndrome: the Sézary signature genes, FCRL3, Tox, and miR-214. Benoit BM, Jariwala N, O'Connor G, Oetjen LK, Whelan TM, Werth A, Troxel AB, Sicard H, Zhu L, Miller C, Takeshita J, McVicar DW, Kim BS, Rook AH, Wysocka M., Free PMC Article | 02/25/2017 |
This study aims to investigate the association between common polymorphisms of FCRL3 gene and multiple sclerosis risk in a Chinese Han population. | Four FCRL3 Gene Polymorphisms (FCRL3_3, _5, _6, _8) Confer Susceptibility to Multiple Sclerosis: Results from a Case-Control Study. Yuan M, Wei L, Zhou R, Bai Q, Wei Y, Zhang W, Huang Y. | 12/17/2016 |
Observed no association between the MHC2TA or FCRL3 SNPs and rheumatoid arthritis in Mexican patients. | MHC2TA and FCRL3 genes are not associated with rheumatoid arthritis in Mexican patients. Mendoza Rincón JF, Rodríguez Elias AK, Fragoso JM, Vargas Alarcón G, Maldonado Murillo K, Rivas Jiménez ML, Barbosa Cobos RE, Jimenez Morales S, Lugo Zamudio G, Tovilla Zárate C, Ramírez Bello J. | 12/17/2016 |
genetic polymorphism is associated with rheumatoid arthritis in Chinese Han population | FCRL3 gene polymorphisms as risk factors for rheumatoid arthritis. Lin X, Zhang Y, Chen Q. | 11/12/2016 |
Genetic polymorphisms in FCRL3 are genetic risk factors for neuromyelitis optica in the Chinese population. | Significant Association Between Fc Receptor-Like 3 Polymorphisms (-1901A>G and -658C>T) and Neuromyelitis Optica (NMO) Susceptibility in the Chinese Population. Wang X, Yu T, Yan Q, Wang W, Meng N, Li X, Luo Y. | 10/8/2016 |
FCRL3_3, FCRL3_5 and FCRL3_6 polymorphisms could increase susceptibility to Graves' disease only in Asians, rather than in Caucasians. | Genetic association of Fc receptor-like glycoprotein with susceptibility to Graves' disease in a Chinese Han population. Fang Y, Li Y, Zeng J, Wang J, Liu R, Cao C. | 08/20/2016 |
CTLA4 and FCRL3 genes overexpression may play an important role in children suffering from autoimmune thyroiditis. | In children with autoimmune thyroiditis CTLA4 and FCRL3 genes--but not PTPN22--are overexpressed when compared to adults. Wojciechowska-Durczynska K, Krawczyk-Rusiecka K, Zygmunt A, Stawerska R, Lewinski A. | 07/30/2016 |
FCRL3 genetic polymorphisms were associated with an increased risk of endometriosis-related infertility, regardless of symptoms. | Association of FCRL3 Genetic Polymorphisms With Endometriosis-Related Infertility Risk: An Independent Study in Han Chinese. Zhang H, Zhang Z, Li G, Wang S, Zhang S, Xie B., Free PMC Article | 02/13/2016 |
4 Single Nucleotide Polymorphisms (rs7528684, rs945635, rs3761959, and rs2282284) could significantly elevate the risk of Neuromyelitis Optica in Chinese Han population. | The Fc Receptor-Like 3 Polymorphisms (rs7528684, rs945635, rs3761959 and rs2282284) and The Risk of Neuromyelitis Optica in A Chinese Population. Lan W, Fang S, Zhang H, Wang DTJ, Wu J., Free PMC Article | 12/19/2015 |
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 | FCRL3 gene polymorphisms confer autoimmunity risk for allergic rhinitis in a Chinese Han population. Gu Z, Hong SL, Ke X, Shen Y, Wang XQ, Hu D, Hu GH, Kang HY., Free PMC Article | 12/12/2015 |
Association between FCRL3 polymorphisms and increased risk of sudden sensorineural hearing loss in a Chinese Han population. | FCRL3 gene polymorphisms confer risk for sudden sensorineural hearing loss in a Chinese Han Population. Liu H, Gu Z, Kang HY, Ke X, Shen Y, Wang XQ, Hu GH, Zeng JH, Hong SL. | 10/10/2015 |