Thrombophilic defects, such as factor V Leiden (FVL) gene mutation may play a role in the pathogenesis of thrombosis in Behcet's disease (BD). Recently, an association of FVL mutation with thrombosis and ocular involvement in BD has been reported. The object of this present study was to ...
mutation 1.Inheritable change in a gene‘s DNA. 2.Change in a gene orgenesof a living cell. A mutation in some way changes the cell’s characteristics and will be inherited.Seechromosome,genes. Dictionary of Unfamiliar Words by Diagram Group Copyright © 2008 by Diagram Visual Information ...
factor V Lei·den -ˈlī-dᵊn 1 : a point mutation producing an abnormal version of factor V that is resistant to inactivation and causes prolonged clotting of blood 2 also factor V Leiden thrombophilia : a genetic disorder caused by factor V Leiden that is marked by an ...
检验第五凝血因子(Factor V leiden)上的G1691A突变：造成容易产生血栓的体质(血栓病, thrombophilia)。北美洲有 5% 的人遗传有莱登第五因子 ( Factor V Leiden )﹐影响凝血功能。 年长﹑肥胖﹑抽烟﹐与及曾经出现过静脉栓塞症状的人士﹐再次...
gender-specific association of the factor v leiden mutation:因子第五因子莱顿突变的性别特异性关联.pdf 2016-11-11上传 gender-specific association of the factor v leiden mutation:因子第五因子莱顿突变的性别特异性关联 文档格式: .pdf 文档大小:
遗传阻断导读:Factor V Leiden易栓症是一种儿科疾病。佳学基因对Factor V Leiden易栓症的发生进行了基因解码,并将之收入《人的基因序列变化与人体疾病表征》中,便于医生选择和使用,进行Factor V Leiden易栓症遗传阻断,也便于患者更好地进行治疗和健康管理。
Factor V Leiden refers to the c.1691G>A variant in the FV gene, which encodes coagulation factor V. This variant results in resistance to factor V protein degradation by activated protein C and increases the risk of VTE 6 to 8 fold in heterozygous carriers and 80 fold in homozygous carrier...
1) Factor V Leiden mutation 凝血因子V Leiden突变 2) Factor V 凝血因子V 1. Preparation and Activity Analysis of PorcineFactor V; 猪凝血因子V的制备及其活性分析 3) Coagulation factor V 凝血因子V 1. Association of activated protein resistance and coagulation factor V gene polymorphism with prethromb...
Factor v Leiden: Pathophysiology and clinical implications Factor V Leiden is the most common inherited risk factor for the development of thrombosis. The factor V Leiden mutation is a single point mutation in the gene coding for factor V, a substitution of adenine for guanine at the nucleotide ...
1. OBJECTIVE: The Factor V Leiden mutation(FVL mutation) represents the most common genetic risk factor for venous thromboembolism. 目的FV Leiden突变是导致静脉血栓栓塞(VTE)的最常见的遗传因素,然而该突变与缺血性脑血管病(ICVD)的关系尚不明确,而且其分布存在种族差异。