• 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

相似文献

1
Cardiovascular Risk and Matrix Metalloproteinase Polymorphisms: Not Just a Simple Substitution.心血管风险与基质金属蛋白酶多态性:并非只是简单的替换
Circ Cardiovasc Genet. 2017 Dec;10(6):e001958. doi: 10.1161/CIRCGENETICS.117.001958.
2
Genetic Variants Contributing to Circulating Matrix Metalloproteinase 8 Levels and Their Association With Cardiovascular Diseases: A Genome-Wide Analysis.影响循环基质金属蛋白酶8水平的基因变异及其与心血管疾病的关联:一项全基因组分析
Circ Cardiovasc Genet. 2017 Dec;10(6). doi: 10.1161/CIRCGENETICS.117.001731.
3
Matrix metalloproteinase-8 and tissue inhibitor of matrix metalloproteinase-1 predict incident cardiovascular disease events and all-cause mortality in a population-based cohort.基质金属蛋白酶-8 和基质金属蛋白酶组织抑制剂-1 可预测基于人群的队列中心血管疾病事件和全因死亡率的发生。
Eur J Prev Cardiol. 2017 Jul;24(11):1136-1144. doi: 10.1177/2047487317706585. Epub 2017 Apr 21.
4
Genetic analysis of polymorphisms in biologically relevant candidate genes in patients with abdominal aortic aneurysms.腹主动脉瘤患者生物学相关候选基因多态性的遗传分析。
J Vasc Surg. 2005 Jun;41(6):1036-42. doi: 10.1016/j.jvs.2005.02.020.
5
Matrix metalloproteinase-1 (MMP-1) and (MMP-8) gene polymorphisms promote increase and remodeling of the collagen III and V in posterior tibial tendinopathy.基质金属蛋白酶-1(MMP-1)和基质金属蛋白酶-8(MMP-8)基因多态性促进胫后肌腱病中III型和V型胶原蛋白的增加和重塑。
Histol Histopathol. 2018 Sep;33(9):929-936. doi: 10.14670/HH-11-982. Epub 2018 Mar 13.
6
Serum tissue-degrading proteinases and incident cardiovascular disease events.血清组织降解蛋白酶与心血管疾病事件的发生。
Eur J Prev Cardiol. 2014 Jul;21(7):806-12. doi: 10.1177/2047487312465524. Epub 2012 Oct 18.
7
Plasma matrix metalloproteinase-9 levels, MMP-9 gene haplotypes, and cardiovascular risk in obese subjects.肥胖受试者的血浆基质金属蛋白酶-9水平、MMP-9基因单倍型与心血管风险
Mol Biol Rep. 2016 Jun;43(6):463-71. doi: 10.1007/s11033-016-3993-z. Epub 2016 May 5.
8
A functional polymorphism in MMP1 could influence osteomyelitis development.基质金属蛋白酶 1 中的一个功能性多态性可能会影响骨髓炎的发展。
J Bone Miner Res. 2010 Apr;25(4):912-9. doi: 10.1359/jbmr.091013.
9
Matrix Matalloproteinase-8 Gene Polymorphism in Chronic Periapical Lesions.慢性根尖周病变中基质金属蛋白酶-8基因多态性
Pril (Makedon Akad Nauk Umet Odd Med Nauki). 2015;36(2):217-24. doi: 10.1515/prilozi-2015-0070.
10
Genetic variability of matrix metalloproteinase genes in cardiovascular disease.基质金属蛋白酶基因在心血管疾病中的遗传变异性。
Curr Top Med Chem. 2012;12(10):1206-13. doi: 10.2174/1568026611208011206.

引用本文的文献

1
The Predictive Role of Plasma Biomarkers in the Evolution of Aortopathies Associated with Congenital Heart Malformations.血浆生物标志物在先天性心脏畸形相关主动脉病变演变中的预测作用。
Int J Mol Sci. 2022 Apr 30;23(9):4993. doi: 10.3390/ijms23094993.
2
Assessment of the correlation between oxidative stress and expression of , and in human aortic smooth muscle cells.评估氧化应激与人类主动脉平滑肌细胞中、和表达之间的相关性。
Arch Med Sci Atheroscler Dis. 2021 Sep 20;6:e158-e165. doi: 10.5114/amsad.2021.109255. eCollection 2021.

本文引用的文献

1
Genetic Variants Contributing to Circulating Matrix Metalloproteinase 8 Levels and Their Association With Cardiovascular Diseases: A Genome-Wide Analysis.影响循环基质金属蛋白酶8水平的基因变异及其与心血管疾病的关联:一项全基因组分析
Circ Cardiovasc Genet. 2017 Dec;10(6). doi: 10.1161/CIRCGENETICS.117.001731.
2
Matrix metalloproteinase family polymorphisms and the risk of aortic aneurysmal diseases: A systematic review and meta-analysis.基质金属蛋白酶家族多态性与主动脉瘤疾病风险:系统评价和荟萃分析。
Clin Genet. 2018 Jan;93(1):15-32. doi: 10.1111/cge.13050. Epub 2017 Jul 18.
3
Relationship of long-term prognosis to MMP and TIMP polymorphisms in patients after ST elevation myocardial infarction.ST段抬高型心肌梗死后患者长期预后与基质金属蛋白酶(MMP)和基质金属蛋白酶组织抑制因子(TIMP)基因多态性的关系。
J Appl Genet. 2017 Aug;58(3):331-341. doi: 10.1007/s13353-016-0388-8. Epub 2017 Jan 18.
4
Matrix Metalloproteinase-2 Polymorphisms in Chronic Heart Failure: Relationship with Susceptibility and Long-Term Survival.慢性心力衰竭中基质金属蛋白酶-2多态性:与易感性和长期生存的关系
PLoS One. 2016 Aug 23;11(8):e0161666. doi: 10.1371/journal.pone.0161666. eCollection 2016.
5
Plasma matrix metalloproteinase-9 levels, MMP-9 gene haplotypes, and cardiovascular risk in obese subjects.肥胖受试者的血浆基质金属蛋白酶-9水平、MMP-9基因单倍型与心血管风险
Mol Biol Rep. 2016 Jun;43(6):463-71. doi: 10.1007/s11033-016-3993-z. Epub 2016 May 5.
6
The MMP-9 -1562 C/T polymorphism in the presence of metabolic syndrome increases the risk of clinical events in patients with coronary artery disease.在代谢综合征存在的情况下,基质金属蛋白酶-9(MMP-9)-1562 C/T基因多态性会增加冠心病患者发生临床事件的风险。
PLoS One. 2014 Sep 5;9(9):e106816. doi: 10.1371/journal.pone.0106816. eCollection 2014.
7
S100A8 and S100A9: DAMPs at the crossroads between innate immunity, traditional risk factors, and cardiovascular disease.S100A8 和 S100A9:固有免疫、传统危险因素和心血管疾病之间的 DAMPs 交汇点。
Mediators Inflamm. 2013;2013:828354. doi: 10.1155/2013/828354. Epub 2013 Dec 22.
8
Sex-specific effect of matrix metalloproteinase-9 functional promoter polymorphism on carotid artery stiffness.基质金属蛋白酶-9 功能启动子多态性对颈动脉僵硬度的性别特异性影响。
Atherosclerosis. 2012 Aug;223(2):416-20. doi: 10.1016/j.atherosclerosis.2012.05.031. Epub 2012 Jun 6.
9
Genetic variants in matrix metalloproteinase-9 gene modify metalloproteinase-9 levels in black subjects.基质金属蛋白酶-9 基因中的遗传变异修饰黑人受试者的基质金属蛋白酶-9 水平。
DNA Cell Biol. 2012 Apr;31(4):504-10. doi: 10.1089/dna.2011.1388. Epub 2011 Sep 21.
10
Association of MMP-8 promoter gene polymorphisms with carotid atherosclerosis: preliminary study.基质金属蛋白酶-8 启动子基因多态性与颈动脉粥样硬化的相关性:初步研究。
Atherosclerosis. 2011 Dec;219(2):673-8. doi: 10.1016/j.atherosclerosis.2011.08.025. Epub 2011 Aug 22.

Cardiovascular Risk and Matrix Metalloproteinase Polymorphisms: Not Just a Simple Substitution.

作者信息

Spinale Francis G, Sapp Ashley A

机构信息

From the Cardiovascular Translational Research Center, University of South Carolina School of Medicine and WJB Dorn Veteran Affairs Medical Center, Columbia (F.G.S., A.A.S.).

出版信息

Circ Cardiovasc Genet. 2017 Dec;10(6):e001958. doi: 10.1161/CIRCGENETICS.117.001958.

DOI:10.1161/CIRCGENETICS.117.001958
PMID:29212903
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5726789/
Abstract
摘要