• 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 prothrombin 20210 A allele is frequently coinherited in young carriers of the factor V Arg 506 to Gln mutation with venous thrombophilia.

作者信息

Ehrenforth S, Ludwig G, Klinke S, Krause M, Scharrer I, Nowak-Gottl U

出版信息

Blood. 1998 Mar 15;91(6):2209-10.

PMID:9490711
Abstract
摘要

相似文献

1
The prothrombin 20210 A allele is frequently coinherited in young carriers of the factor V Arg 506 to Gln mutation with venous thrombophilia.凝血酶原20210 A等位基因在因子V Arg 506至Gln突变且患有静脉血栓形成倾向的年轻携带者中经常共同遗传。
Blood. 1998 Mar 15;91(6):2209-10.
2
The A20210 allele of the prothrombin gene is frequently associated with the factor V Arg 506 to Gln mutation but not with protein S deficiency in thrombophilic families.凝血酶原基因的A20210等位基因在血栓形成倾向家族中常与因子V精氨酸506突变为谷氨酰胺相关，但与蛋白S缺乏无关。
Blood. 1998 Mar 15;91(6):2210-1.
3
Type and location of venous thromboembolism in carriers of Factor V Leiden or prothrombin G20210A mutation versus patients with no mutation.携带因子 V 莱顿或凝血酶原 G20210A 突变的患者与无突变患者的静脉血栓栓塞类型和位置。
Clin Appl Thromb Hemost. 2010 Feb;16(1):66-70. doi: 10.1177/1076029608320721. Epub 2008 Sep 15.
4
Prevalence of factor V Leiden and prothrombin G20210A gene mutation.
Saudi Med J. 2005 Nov;26(11):1844.
5
Combined carrier status of prothrombin 20210A and factor XIII-A Leu34 alleles as a strong risk factor for myocardial infarction: evidence of a gene-gene interaction.凝血酶原20210A和凝血因子XIII-A Leu34等位基因的联合携带状态作为心肌梗死的强风险因素：基因-基因相互作用的证据
Blood. 2003 Apr 15;101(8):3037-41. doi: 10.1182/blood-2002-09-2888. Epub 2002 Dec 12.
6
The heterozygous 20210 G/A prothrombin genotype is associated with early venous thrombosis in inherited thrombophilias and is not increased in frequency in artery disease.
Arterioscler Thromb Vasc Biol. 1997 Nov;17(11):2418-22. doi: 10.1161/01.atv.17.11.2418.
7
Rapid simultaneous screening of factor V Leiden and G20210A prothrombin variant by multiplex polymerase chain reaction on whole blood.
Blood. 1998 Mar 15;91(6):2208-9.
8
A Study on Hereditary Thrombophilia and Stroke in a Cohort from Sri Lanka.斯里兰卡一组人群中遗传性血栓形成倾向与中风的研究
J Stroke Cerebrovasc Dis. 2016 Jan;25(1):102-9. doi: 10.1016/j.jstrokecerebrovasdis.2015.08.042. Epub 2015 Oct 27.
9
Thrombophilic risk of individuals with rare compound factor V Leiden and prothrombin G20210A polymorphisms: an international case series of 100 individuals.具有罕见复合因子V莱顿突变和凝血酶原G20210A多态性个体的血栓形成风险：100例个体的国际病例系列
Eur J Haematol. 2016 Oct;97(4):353-60. doi: 10.1111/ejh.12738. Epub 2016 Feb 18.
10
Co-inheritance of the 20210A allele of the prothrombin gene increases the risk of thrombosis in subjects with familial thrombophilia.凝血酶原基因20210A等位基因的共同遗传增加了家族性血栓形成倾向患者发生血栓形成的风险。
Thromb Haemost. 1997 Dec;78(6):1426-9.

引用本文的文献

1
Phenotypic Heterogeneity in Patients with Homozygous Prothrombin 20210AA Genotype. A paper from the 2005 William Beaumont Hospital Symposium on Molecular Pathology.纯合子凝血酶原20210AA基因型患者的表型异质性。一篇来自2005年威廉·博蒙特医院分子病理学研讨会的论文。
J Mol Diagn. 2006 Sep;8(4):420-5. doi: 10.2353/jmoldx.2006.060014.
2
Congenital thrombophilia and thrombosis: a study in a single centre.先天性血栓形成倾向与血栓形成：单中心研究
Arch Dis Child. 1999 Aug;81(2):176-8. doi: 10.1136/adc.81.2.176.