• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

The polymorphisms -1131T>C and the S19W of the APOA5 gene are not associated with coronary artery disease in a Brazilian population.

作者信息

Prochaska Caroline Luise, Picheth Geraldo, Anghebem-Oliveira Mauren Isfer, Costantini Costantino Ortiz, de Souza Emanuel Maltempi, Pedrosa Fábio Oliveira, Scartezini Marileia

机构信息

Department of Medical Pathology, Universidade Federal do Paraná, Curitiba, Paraná, Brazil.

出版信息

Clin Chem Lab Med. 2010 Mar;48(3):419-22. doi: 10.1515/CCLM.2010.070.

DOI:10.1515/CCLM.2010.070
PMID:20170397
Abstract
摘要

相似文献

1
The polymorphisms -1131T>C and the S19W of the APOA5 gene are not associated with coronary artery disease in a Brazilian population.载脂蛋白A5基因的-1131T>C和S19W多态性与巴西人群的冠状动脉疾病无关。
Clin Chem Lab Med. 2010 Mar;48(3):419-22. doi: 10.1515/CCLM.2010.070.
2
Apolipoprotein A-V: a potential modulator of plasma triglyceride levels in Turks.载脂蛋白A-V:土耳其人血浆甘油三酯水平的潜在调节因子。
J Lipid Res. 2006 Jan;47(1):144-53. doi: 10.1194/jlr.M500343-JLR200. Epub 2005 Oct 28.
3
The apolipoprotein A5 -1131T>C promoter polymorphism in Koreans: association with plasma APOA5 and serum triglyceride concentrations, LDL particle size and coronary artery disease.韩国人中载脂蛋白A5 -1131T>C启动子多态性:与血浆载脂蛋白A5、血清甘油三酯浓度、低密度脂蛋白颗粒大小及冠状动脉疾病的关联
Clin Chim Acta. 2009 Apr;402(1-2):83-7. doi: 10.1016/j.cca.2008.12.024. Epub 2008 Dec 31.
4
APOA5 polymorphisms influence plasma triglycerides in young, healthy African Americans and whites of the CARDIA Study.载脂蛋白A5基因多态性影响年轻健康非裔美国人和白人动脉粥样硬化风险发展研究(CARDIA研究)中的血浆甘油三酯水平。
J Lipid Res. 2005 Mar;46(3):564-71. doi: 10.1194/jlr.M400437-JLR200. Epub 2004 Dec 16.
5
The -1131 T>C and S19W APOA5 gene polymorphisms are associated with high levels of triglycerides and apolipoprotein C-III, but not with coronary artery disease: an angiographic study.-1131 T>C和S19W载脂蛋白A5(APOA5)基因多态性与高甘油三酯水平和载脂蛋白C-III相关,但与冠状动脉疾病无关:一项血管造影研究。
Atherosclerosis. 2007 Apr;191(2):409-17. doi: 10.1016/j.atherosclerosis.2006.04.009. Epub 2006 May 8.
6
Association of PON1 and APOA5 gene polymorphisms in a cohort of Indian patients having coronary artery disease with and without type 2 diabetes.印度冠心病患者队列中伴有或不伴有2型糖尿病的对氧磷酶1(PON1)和载脂蛋白A5(APOA5)基因多态性的关联研究
Genet Test Mol Biomarkers. 2011 Jul-Aug;15(7-8):507-12. doi: 10.1089/gtmb.2010.0207. Epub 2011 Mar 25.
7
Mutation screening of the APOA5 gene in subjects with coronary artery disease.载脂蛋白 A5 基因在冠心病患者中的突变筛查。
J Investig Med. 2012 Oct;60(7):1015-9. doi: 10.2310/JIM.0b013e3182686918.
8
Association of APOA1 and APOA5 polymorphisms and haplotypes with lipid parameters in a Brazilian elderly cohort.巴西老年队列中APOA1和APOA5基因多态性及单倍型与血脂参数的关联
Genet Mol Res. 2013 Feb 28;12(3):3495-9. doi: 10.4238/2013.February.28.7.
9
APOA5 gene polymorphism modulates levels of triglyceride, HDL cholesterol and FERHDL but is not a risk factor for coronary artery disease.载脂蛋白A5基因多态性可调节甘油三酯、高密度脂蛋白胆固醇和富含甘油三酯的高密度脂蛋白水平,但并非冠状动脉疾病的危险因素。
Atherosclerosis. 2004 Sep;176(1):165-72. doi: 10.1016/j.atherosclerosis.2004.04.024.
10
Association of USF1 and APOA5 polymorphisms with familial combined hyperlipidemia in an Italian population.美国佛罗里达大学1号因子(USF1)和载脂蛋白A5(APOA5)基因多态性与意大利人群家族性混合性高脂血症的关联
Mol Cell Probes. 2015 Feb;29(1):19-24. doi: 10.1016/j.mcp.2014.10.002. Epub 2014 Oct 13.

引用本文的文献

1
Apolipoprotein A5 gene polymorphism (rs662799) and cardiovascular disease in end-stage kidney disease patients.载脂蛋白 A5 基因多态性(rs662799)与终末期肾病患者的心血管疾病。
BMC Nephrol. 2022 Sep 7;23(1):307. doi: 10.1186/s12882-022-02925-1.
2
Association of c.56C > G (rs3135506) Apolipoprotein A5 Gene Polymorphism with Coronary Artery Disease in Moroccan Subjects: A Case-Control Study and an Updated Meta-Analysis.摩洛哥人群中载脂蛋白A5基因c.56C > G(rs3135506)多态性与冠状动脉疾病的关联:一项病例对照研究及更新的荟萃分析
Cardiol Res Pract. 2020 Aug 4;2020:5981971. doi: 10.1155/2020/5981971. eCollection 2020.
3
Analysis of causal effect of APOA5 variants on premature coronary artery disease.
载脂蛋白A5基因变异对早发性冠状动脉疾病的因果效应分析。
Ann Hum Genet. 2018 Nov;82(6):437-447. doi: 10.1111/ahg.12273. Epub 2018 Jul 19.
4
Association of APOA5 Gene Promoter Region -1131T>C Polymorphism (rs662799) to Plasma Triglyceride Level in Patients with Type 2 Diabetic Nephropathy.2型糖尿病肾病患者中APOA5基因启动子区域-1131T>C多态性(rs662799)与血浆甘油三酯水平的关联
J Clin Diagn Res. 2016 May;10(5):BC09-13. doi: 10.7860/JCDR/2016/19212.7895. Epub 2016 May 1.
5
Association of G894T eNOS, 4G/5G PAI and T1131C APOA5 polymorphisms with susceptibility to myocardial infarction in Morocco.G894T内皮型一氧化氮合酶、4G/5G纤溶酶原激活物抑制剂及T1131C载脂蛋白A5基因多态性与摩洛哥人心肌梗死易感性的关联
Meta Gene. 2016 Apr 3;9:56-61. doi: 10.1016/j.mgene.2016.03.004. eCollection 2016 Sep.
6
Apolipoprotein A5 and apolipoprotein C3 single nucleotide polymorphisms are correlated with an increased risk of coronary heart disease: a case-control and meta-analysis study.载脂蛋白A5和载脂蛋白C3单核苷酸多态性与冠心病风险增加相关:一项病例对照和荟萃分析研究。
Lipids Health Dis. 2015 Sep 19;14:113. doi: 10.1186/s12944-015-0110-6.
7
Association of APOA5 T1131C polymorphism and risk of coronary artery disease.APOA5基因T1131C多态性与冠状动脉疾病风险的关联。
Int J Clin Exp Med. 2015 Jun 15;8(6):8986-94. eCollection 2015.
8
Positive Association between APOA5 rs662799 Polymorphism and Coronary Heart Disease: A Case-Control Study and Meta-Analysis.APOA5基因rs662799多态性与冠心病之间的正相关关系:一项病例对照研究及荟萃分析
PLoS One. 2015 Aug 26;10(8):e0135683. doi: 10.1371/journal.pone.0135683. eCollection 2015.
9
Apolipoprotein A5 gene variants and the risk of coronary heart disease: a case‑control study and meta‑analysis.载脂蛋白 A5 基因变异与冠心病风险:病例对照研究和荟萃分析。
Mol Med Rep. 2013 Oct;8(4):1175-82. doi: 10.3892/mmr.2013.1642. Epub 2013 Aug 16.
10
-1131T>C and SW19 polymorphisms in APOA5 gene and lipid levels in type 2 diabetic patients.载脂蛋白 A5 基因的-1131T>C 和 SW19 多态性与 2 型糖尿病患者的血脂水平。
Mol Biol Rep. 2012 Jul;39(7):7541-8. doi: 10.1007/s11033-012-1588-x. Epub 2012 Feb 19.