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...
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 leiden mutation and Budd-Chiari syndrome. Blood 1998;92:1838,1839.Mohanty D, Shetty S, Narayanan TS, Abraham P. Factor V Leiden muta- tion and Budd-Chiari syndrome. Blood 1998;92:1838-1839.Mohanty D, Shetty S, Narayanan TS, Abraham P. Factor V Leiden mutation and Budd Chiari...
Defects in the Factor V gene can result various diseases including Factor V deficiency, thrombophilia due to activated protein C resistance, Budd-Chiari syndrome, Ischemic stroke, and recurrent pregnancy loss. 仅用于科研。不用于诊断过程。未经明确授权不得转售。
Synonyms for Factor V Leiden mutation in Free Thesaurus. Antonyms for Factor V Leiden mutation. 34 synonyms for mutation: anomaly, variation, deviant, freak of nature, change, variation, evolution, transformation, modification, alteration, deviation...
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...
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...
5-10 µg/mL - 产品规格 种属反应 Human 宿主/亚型 Mouse / IgG 分类 Monoclonal 类型 Antibody 克隆号 5146 抗原 Human factor V and heavy chain of factor Va. 偶联物 Unconjugated 形式 Liquid 浓度 9.2 mg/mL 纯化类型 SDS-PAGE 保存液 50% water with 50% glyc...
A single missense mutation (R506Q) due to a G/A transition (G1691A) in exon 10 of the factor V gene is regarded as the causative molecular defect, resulting in factor V Leiden which is correlated with APCR. Identification of this mutation by polymerase chain reaction-based methods is ...
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 ...