• 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
Genetics of atherothrombotic and lacunar stroke.动脉粥样硬化血栓形成性和腔隙性卒中的遗传学
Circ Cardiovasc Genet. 2009 Apr;2(2):191-8. doi: 10.1161/CIRCGENETICS.108.828319.
2
Tissue plasminogen activator -7351C/T polymorphism and lacunar stroke.组织型纤溶酶原激活剂-7351C/T多态性与腔隙性卒中
Stroke. 2006 Feb;37(2):329; author reply 329-30. doi: 10.1161/01.STR.0000199663.64894.4f. Epub 2005 Dec 29.
3
Fibrinogen gene promoter -455 A allele as a risk factor for lacunar stroke.纤维蛋白原基因启动子-455 A等位基因作为腔隙性卒中的一个危险因素。
Stroke. 2003 Apr;34(4):886-91. doi: 10.1161/01.STR.0000060029.23872.55. Epub 2003 Mar 13.
4
Tissue plasminogen activator -7351C/T enhancer polymorphism is a risk factor for lacunar stroke.组织型纤溶酶原激活剂-7351C/T增强子多态性是腔隙性卒中的一个危险因素。
Stroke. 2004 May;35(5):1090-4. doi: 10.1161/01.STR.0000124123.76658.6c. Epub 2004 Mar 18.
5
Family history of stroke is an independent risk factor for lacunar stroke subtype with asymptomatic lacunar infarcts at younger ages.家族性卒中史是腔隙性卒中亚型的独立危险因素，其无症状腔隙性梗死发生在年龄较轻的人群中。
Stroke. 2011 May;42(5):1196-200. doi: 10.1161/STROKEAHA.110.602383. Epub 2011 Mar 24.
6
[A study of association between atherothrombotic brain infarction and HLA-DQA1 peptide binding motifs].动脉粥样硬化血栓形成性脑梗死与HLA - DQA1肽结合基序之间的关联研究
Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2001 Aug;18(4):272-5.
7
Estimating the magnitude of genetic factors by calculating the genetic relative risk of stroke in first-ever lacunar stroke patients.通过计算首发腔隙性脑卒中患者的脑卒中遗传相对风险来估计遗传因素的大小。
PLoS One. 2011;6(6):e21439. doi: 10.1371/journal.pone.0021439. Epub 2011 Jun 29.
8
Ischaemic stroke patients with heterozygous factor V Leiden present with multiple brain infarctions and widespread atherothrombotic disease.患有杂合子因子V莱顿突变的缺血性中风患者会出现多发性脑梗死和广泛的动脉粥样硬化血栓形成疾病。
Thromb Haemost. 2009 Jan;101(1):145-50.
9
Promoter variant of angiopoietin-2 and plasma angiopoietin-2 are associated with risk of stroke recurrence in lacunar infarct patients.血管生成素-2 启动子变异体和血浆血管生成素-2 与腔隙性梗死患者卒中复发风险相关。
Biochem Biophys Res Commun. 2010 Jul 23;398(2):212-6. doi: 10.1016/j.bbrc.2010.06.062. Epub 2010 Jun 18.
10
Association of PRKCH gene with lacunar infarction in a local Chinese Han population.PRKCH基因与中国当地汉族人群腔隙性脑梗死的相关性
Neurosci Lett. 2009 Oct 23;464(2):146-9. doi: 10.1016/j.neulet.2009.08.046. Epub 2009 Aug 22.

引用本文的文献

1
Dissecting Polygenic Etiology of Ischemic Stroke in the Era of Precision Medicine.精准医学时代缺血性卒中多基因病因剖析
J Clin Med. 2022 Oct 11;11(20):5980. doi: 10.3390/jcm11205980.
2
Increased risk of stroke in oral contraceptive users carried replicated genetic variants: a population-based case-control study in China.口服避孕药使用者中风风险增加与携带可重复的遗传变异有关：中国基于人群的病例对照研究。
Hum Genet. 2012 Aug;131(8):1337-44. doi: 10.1007/s00439-012-1161-7. Epub 2012 Apr 4.
3
Heterogeneity of the phenotypic definition of coronary artery disease and its impact on genetic association studies.冠状动脉疾病表型定义的异质性及其对基因关联研究的影响。
Circ Cardiovasc Genet. 2011 Feb;4(1):58-67. doi: 10.1161/CIRCGENETICS.110.957738. Epub 2010 Dec 13.

本文引用的文献

1
Cardiovascular genomics, personalized medicine, and the National Heart, Lung, and Blood Institute: part I: the beginning of an era.心血管基因组学、个性化医疗与美国国立心肺血液研究所：第一部分：一个时代的开端
Circ Cardiovasc Genet. 2008 Oct;1(1):51-7. doi: 10.1161/CIRCGENETICS.108.813337.
2
Genetic polymorphisms for the study of multifactorial stroke.用于多因素中风研究的基因多态性。
Hum Mutat. 2008 Jun;29(6):776-95. doi: 10.1002/humu.20666.
3
Variation in the PDE4D gene and ischemic stroke risk: a systematic review and meta-analysis on 5200 cases and 6600 controls.磷酸二酯酶4D基因变异与缺血性中风风险：对5200例病例和6600例对照的系统评价和荟萃分析
Stroke. 2008 Jul;39(7):1966-71. doi: 10.1161/STROKEAHA.107.509992. Epub 2008 Apr 17.
4
Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes.全基因组关联数据的荟萃分析及大规模重复研究确定了2型糖尿病的其他易感基因座。
Nat Genet. 2008 May;40(5):638-45. doi: 10.1038/ng.120. Epub 2008 Mar 30.
5
Genetic variation in members of the leukotriene biosynthesis pathway confer an increased risk of ischemic stroke: a replication study in two independent populations.白三烯生物合成途径成员的基因变异会增加缺血性中风的风险：在两个独立人群中的重复研究。
Stroke. 2008 Apr;39(4):1109-14. doi: 10.1161/STROKEAHA.107.491969. Epub 2008 Mar 6.
6
Association and linkage disequilibrium analyses of APOE polymorphisms in atherosclerosis.载脂蛋白E基因多态性在动脉粥样硬化中的关联分析和连锁不平衡分析
Dis Markers. 2008;24(2):65-72. doi: 10.1155/2008/650410.
7
Designing candidate gene and genome-wide case-control association studies.设计候选基因和全基因组病例对照关联研究。
Nat Protoc. 2007;2(10):2492-501. doi: 10.1038/nprot.2007.366.
8
Genes, endothelial function and cerebral small vessel disease in man.人类的基因、内皮功能与脑小血管疾病
Exp Physiol. 2008 Jan;93(1):121-7. doi: 10.1113/expphysiol.2007.038752. Epub 2007 Oct 12.
9
ACE I/D polymorphism in Korean patients with ischemic stroke and silent brain infarction.韩国缺血性脑卒中及无症状脑梗死患者的ACE I/D基因多态性
Acta Neurol Scand. 2008 Apr;117(4):244-9. doi: 10.1111/j.1600-0404.2007.00932.x. Epub 2007 Oct 8.
10
Paraoxonase/arylesterase ratio, PON1 192Q/R polymorphism and PON1 status are associated with increased risk of ischemic stroke.对氧磷酶/芳基酯酶比值、对氧磷酶1（PON1）192Q/R多态性及对氧磷酶1状态与缺血性中风风险增加相关。
Clin Biochem. 2008 Jan;41(1-2):1-9. doi: 10.1016/j.clinbiochem.2007.08.010. Epub 2007 Aug 24.

Genetics of atherothrombotic and lacunar stroke.

作者信息

Debette Stéphanie, Seshadri Sudha

机构信息

Department of Neurology, Boston University School of Medicine, 72 East Concord Street, Boston, MA 02118-2526, USA.

出版信息

Circ Cardiovasc Genet. 2009 Apr;2(2):191-8. doi: 10.1161/CIRCGENETICS.108.828319.

DOI:10.1161/CIRCGENETICS.108.828319
PMID:20031584
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2798146/
Abstract
摘要