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Meta-analysis evidence of a differential risk of the FCRL3 -169T-->C polymorphism in white and East Asian rheumatoid arthritis patients.

作者信息

Begovich Ann B, Chang Monica, Schrodi Steven J

机构信息

Celera, Alameda, CA, USA.

出版信息

Arthritis Rheum. 2007 Sep;56(9):3168-71. doi: 10.1002/art.22857.

DOI:10.1002/art.22857
PMID:17763442
Abstract
摘要

相似文献

1
Meta-analysis evidence of a differential risk of the FCRL3 -169T-->C polymorphism in white and East Asian rheumatoid arthritis patients.FCRL3基因-169T→C多态性在白种人和东亚类风湿关节炎患者中存在差异风险的Meta分析证据。
Arthritis Rheum. 2007 Sep;56(9):3168-71. doi: 10.1002/art.22857.
2
FCRL3 gene polymorphisms as risk factors for rheumatoid arthritis.FCRL3基因多态性作为类风湿性关节炎的危险因素
Hum Immunol. 2016 Feb;77(2):223-9. doi: 10.1016/j.humimm.2015.12.007. Epub 2015 Dec 31.
3
The functional -169T-->C single-nucleotide polymorphism in FCRL3 is not associated with rheumatoid arthritis in white North Americans.FCRL3基因中功能性的-169T→C单核苷酸多态性与北美白人的类风湿性关节炎无关。
Arthritis Rheum. 2006 Mar;54(3):1022-5. doi: 10.1002/art.21636.
4
An updated meta-analysis of the Fc receptor-like 3 -169T/C polymorphism and rheumatoid arthritis risk.Fc 受体样蛋白 3-169T/C 多态性与类风湿关节炎风险的一项更新的荟萃分析。
Scand J Rheumatol. 2013;42(4):270-5. doi: 10.3109/03009742.2012.754938. Epub 2013 Mar 7.
5
Association between functional Fc receptor-like 3 (FCRL3) -169 C/T polymorphism and susceptibility to seropositive rheumatoid arthritis in Asians: a meta-analysis.功能 Fc 受体样 3（FCRL3）-169 C/T 多态性与亚洲人血清阳性类风湿关节炎易感性的关联：一项荟萃分析。
Hum Immunol. 2013 Sep;74(9):1206-13. doi: 10.1016/j.humimm.2013.05.018. Epub 2013 Jun 15.
6
The FCRL3 -169T>C polymorphism is associated with rheumatoid arthritis and shows suggestive evidence of involvement with juvenile idiopathic arthritis in a Scandinavian panel of autoimmune diseases.FCRL3基因-169T>C多态性与类风湿性关节炎相关，并且在一组斯堪的纳维亚自身免疫性疾病中显示出与青少年特发性关节炎有关的提示性证据。
Ann Rheum Dis. 2008 Sep;67(9):1287-91. doi: 10.1136/ard.2007.077826. Epub 2007 Dec 7.
7
FCRL3 -169C/C genotype is associated with anti-citrullinated protein antibody-positive rheumatoid arthritis and with radiographic progression.FCRL3-169C/C 基因型与抗瓜氨酸化蛋白抗体阳性类风湿关节炎和放射学进展相关。
J Rheumatol. 2011 Nov;38(11):2329-35. doi: 10.3899/jrheum.110489. Epub 2011 Sep 1.
8
Fc receptor-like 3 -169 C/T polymorphism and RA susceptibility: a meta-analysis.Fc 受体样 3-169C/T 多态性与 RA 易感性的关联：一项荟萃分析。
Rheumatol Int. 2010 May;30(7):947-53. doi: 10.1007/s00296-009-1082-5. Epub 2009 Aug 19.
9
MHC2TA and FCRL3 genes are not associated with rheumatoid arthritis in Mexican patients.MHC2TA和FCRL3基因与墨西哥患者的类风湿性关节炎无关。
Rheumatol Int. 2016 Feb;36(2):249-54. doi: 10.1007/s00296-015-3358-2. Epub 2015 Sep 8.
10
The FCRL3 -169T>C polymorphism might be associated with some autoantibody presence in patients with SLE in a Polish population.FCRL3基因-169T>C多态性可能与波兰人群系统性红斑狼疮患者体内某些自身抗体的存在有关。
Mod Rheumatol. 2014 Mar;24(2):296-9. doi: 10.3109/14397595.2013.854066.

引用本文的文献

1
Association of Optic Neuritis with Gene Single Nucleotide Polymorphism and IL-17A Concentration.视神经炎与基因单核苷酸多态性及白细胞介素-17A浓度的关联
J Ophthalmol. 2018 Mar 15;2018:1686297. doi: 10.1155/2018/1686297. eCollection 2018.
2
The Fc Receptor-Like 3 Polymorphisms (rs7528684, rs945635, rs3761959 and rs2282284) and The Risk of Neuromyelitis Optica in A Chinese Population.Fc 受体样 3 基因多态性（rs7528684、rs945635、rs3761959 和 rs2282284）与中国人群视神经脊髓炎的风险
Medicine (Baltimore). 2015 Sep;94(38):e1320. doi: 10.1097/MD.0000000000001320.
3
MHC2TA and FCRL3 genes are not associated with rheumatoid arthritis in Mexican patients.
MHC2TA和FCRL3基因与墨西哥患者的类风湿性关节炎无关。
Rheumatol Int. 2016 Feb;36(2):249-54. doi: 10.1007/s00296-015-3358-2. Epub 2015 Sep 8.
4
Four FCRL3 Gene Polymorphisms (FCRL3_3, _5, _6, _8) Confer Susceptibility to Multiple Sclerosis: Results from a Case-Control Study.四个FCRL3基因多态性（FCRL3_3、_5、_6、_8）赋予多发性硬化症易感性：一项病例对照研究的结果。
Mol Neurobiol. 2016 Apr;53(3):2029-2035. doi: 10.1007/s12035-015-9149-7. Epub 2015 Apr 11.
5
A systems genetics approach provides a bridge from discovered genetic variants to biological pathways in rheumatoid arthritis.系统遗传学方法为从已发现的遗传变异到类风湿关节炎的生物途径提供了桥梁。
PLoS One. 2011;6(9):e25389. doi: 10.1371/journal.pone.0025389. Epub 2011 Sep 28.
6
[Genetics of rheumatoid arthritis].[类风湿关节炎的遗传学]
Z Rheumatol. 2011 Apr;70(3):186-8, 190-1. doi: 10.1007/s00393-010-0690-5.
7
Expression of the autoimmune susceptibility gene FcRL3 on human regulatory T cells is associated with dysfunction and high levels of programmed cell death-1.自身免疫易感性基因 FcRL3 在人调节性 T 细胞上的表达与功能障碍和程序性细胞死亡-1 高水平相关。
J Immunol. 2010 Apr 1;184(7):3639-47. doi: 10.4049/jimmunol.0903943. Epub 2010 Feb 26.
8
Fc receptor-like 3 -169 C/T polymorphism and RA susceptibility: a meta-analysis.Fc 受体样 3-169C/T 多态性与 RA 易感性的关联：一项荟萃分析。
Rheumatol Int. 2010 May;30(7):947-53. doi: 10.1007/s00296-009-1082-5. Epub 2009 Aug 19.
9
Polymorphisms of FCRL3 in a Chinese population with Vogt-Koyanagi-Harada (VKH) syndrome.中国Vogt-小柳-原田（VKH）综合征患者中FCRL3基因多态性研究
Mol Vis. 2009 May 11;15:955-61.
10
A large-scale rheumatoid arthritis genetic study identifies association at chromosome 9q33.2.一项大规模类风湿性关节炎基因研究确定了9号染色体q33.2区域的关联。
PLoS Genet. 2008 Jun 27;4(6):e1000107. doi: 10.1371/journal.pgen.1000107.