Suppr超能文献

[缺血性心脏病早期发展患者止血因子基因的多态性。]

[Polymorphism of genes of factors of hemostasis in patients with early development of ischemic heart disease.].

作者信息

Dankovtseva E N, Zateĭshchikov D A, Sidorenko B A

机构信息

Presidential Medical Center of Russia; ul. Marshala Timoshenko, 15, 121356 Moscow, Russia.

出版信息

Kardiologiia. 2006;46(2):56-65.

Abstract

The review is devoted to analysis of data, related to contribution of genetic peculiarities of the hemostasis system to early development of ischemic heart disease (IHD). Information is presented on polymorphisms of tissue factor, coagulation factors VII, V, prothrombin, thrombomodulin, fibrinogen, thrombin activated fibrinolysis inhibitor, tissue plasminogen activator inhibitor, platelet membrane glycoproteines Ia, Iba, IIIa in patients with early development of IHD. Contradictoriness of existing data on effects of genetic heterogeneity of factors of hemostasis on risk of development of IHD at young age and necessity of further investigations in this area are underlined.

摘要

本综述致力于分析与止血系统遗传特性对缺血性心脏病(IHD)早期发展的贡献相关的数据。文中介绍了IHD早期发病患者中组织因子、凝血因子VII、V、凝血酶原、血栓调节蛋白、纤维蛋白原、凝血酶激活的纤溶抑制物、组织型纤溶酶原激活物抑制剂、血小板膜糖蛋白Ia、Iba、IIIa的多态性。强调了现有关于止血因子遗传异质性对年轻时IHD发病风险影响的数据存在矛盾性,以及该领域进一步研究的必要性。

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