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The functional -169T-->C single-nucleotide polymorphism in FCRL3 is not associated with rheumatoid arthritis in white North Americans.

作者信息

Hu Xiaolan, Chang Monica, Saiki Randall K, Cargill Michelle A, Begovich Ann B, Ardlie Kristin G, Criswell Lindsey A, Seldin Michael F, Amos Christopher I, Gregersen Peter K, Kastner Daniel L, Remmers Elaine F

机构信息

Celera Diagnostics, Alameda, CA.

出版信息

Arthritis Rheum. 2006 Mar;54(3):1022-5. doi: 10.1002/art.21636.

DOI:10.1002/art.21636
PMID:16508985
Abstract
摘要

相似文献

1
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.
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 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.
4
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.
5
Disease phenotypes and gender association of FCRL3 single-nucleotide polymorphism -169T/C in Taiwanese patients with systemic lupus erythematosus and rheumatoid arthritis.台湾地区系统性红斑狼疮和类风湿关节炎患者 FCRL3 单核苷酸多态性-169T/C 与疾病表型和性别相关性。
J Rheumatol. 2011 Feb;38(2):264-70. doi: 10.3899/jrheum.100437. Epub 2010 Nov 15.
6
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.
7
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.
8
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.
9
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.
10
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.

引用本文的文献

1
Comorbidities of rheumatoid arthritis: Results from the Korean National Health and Nutrition Examination Survey.类风湿关节炎的合并症：韩国国民健康与营养检查调查结果
PLoS One. 2017 Apr 19;12(4):e0176260. doi: 10.1371/journal.pone.0176260. eCollection 2017.
2
Pooled genome wide association detects association upstream of FCRL3 with Graves' disease.全基因组关联分析揭示FCRL3基因上游区域与格雷夫斯病的关联。
BMC Genomics. 2016 Nov 18;17(1):939. doi: 10.1186/s12864-016-3276-z.
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
Association of FCRL4 polymorphisms on disease susceptibility and severity of ankylosing spondylitis in Chinese Han population.FCRL4 多态性与中国汉族人群强直性脊柱炎易感性及严重程度的相关性。
Clin Rheumatol. 2012 Oct;31(10):1449-54. doi: 10.1007/s10067-012-2028-y. Epub 2012 Jul 10.
6
Caucasian and Asian specific rheumatoid arthritis risk loci reveal limited replication and apparent allelic heterogeneity in north Indians.高加索人和亚洲人特有的类风湿关节炎风险基因座在北印度人中显示出有限的复制和明显的等位基因异质性。
PLoS One. 2012;7(2):e31584. doi: 10.1371/journal.pone.0031584. Epub 2012 Feb 15.
7
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.
8
No significant association between Fc receptor-like 3 gene polymorphisms and human leukocyte antigen-B27 positive ankylosing spondylitis in Han Chinese population.汉族人群中Fc受体样3基因多态性与人类白细胞抗原-B27阳性强直性脊柱炎之间无显著关联。
Mol Biol Rep. 2010 Jan;37(1):297-300. doi: 10.1007/s11033-009-9690-4. Epub 2009 Aug 6.
9
Genetic risk factors for rheumatoid arthritis differ in Caucasian and Korean populations.类风湿关节炎的遗传风险因素在白种人和韩国人群中存在差异。
Arthritis Rheum. 2009 Feb;60(2):364-71. doi: 10.1002/art.24245.
10
FCRL3 promoter 169 CC homozygosity is associated with susceptibility to rheumatoid arthritis in Dutch Caucasians.FCRL3基因启动子169位点CC纯合性与荷兰白种人患类风湿关节炎的易感性相关。
Ann Rheum Dis. 2007 Jun;66(6):803-6. doi: 10.1136/ard.2006.064949. Epub 2006 Dec 19.