In a wild type individual, the factor V protein activates prothrombin to form thrombin, which is involed in the clotting pathway. Factor V Leiden is a variant of the factor V protein, with a G> A substitution at nucleotide position 1,691 in the F5 gene. The substitution leads to aV ...
“Factor V Leiden.” Merriam-Webster.com Medical Dictionary, Merriam-Webster, https://www.merriam-webster.com/medical/factor%20V%20Leiden. Accessed 16 Dec. 2024. Copy Citation Share Post the Definition of factor V Leiden to Facebook Facebook Share the Definition of factor V Leiden on Tw...
Factor V Leiden 第五凝血因子；莱登第五因子 第五凝血因子 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...
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...
factor-V Leidenfactor-V Leiden A common mutation of coagulation factor-V gene, which is found in 3 to 8% of Caucasians, and results in resistance to activated C protein and an increased risk in deep-vein and other thromboses. Segen's Medical Dictionary. © 2012 Farlex, Inc. All rights...
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易栓症疾病介绍: Factor V Leiden易栓症是一种遗传性血液凝固障碍。Factor V Leiden是导致易...
Factor V (FV) Leiden is the most common genetic risk factor for venous thrombosis. It is caused by a single point mutation in the factor V gene ( F5 ), which results in the replacement of arginine at position 506 with a glutamine. Arginine 506 constitutes one of three cleavage sites for...
网络第五凝血因子;莱登第五因子 网络释义
b.The process by which such a change occurs, either through an alteration in the nucleotide sequence coding for a gene or through a change in the physical arrangement of the genetic material. c.The nucleotide sequence, trait, or individual that results from such a change. ...
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: