Cross talk pathways between coagulation and inflammation

JH Foley, EM Conway - Circulation research, 2016 - Am Heart Assoc
Anatomic pathology studies performed over 150 years ago revealed that excessive
activation of coagulation occurs in the setting of inflammation. However, it has taken over a …

Uncertain thrombophilia markers

M Franchini, I Martinelli… - Thrombosis and …, 2016 - thieme-connect.com
The development of venous thromboembolism (VTE), which includes deep-vein thrombosis
and pulmonary embolism, may be associated with inherited or acquired risk factors that can …

Multilocus genetic risk scores for venous thromboembolism risk assessment

JM Soria, PE Morange, J Vila, JC Souto… - Journal of the …, 2014 - Am Heart Assoc
Background Genetics plays an important role in venous thromboembolism (VTE). Factor V
Leiden (FVL or rs6025) and prothrombin gene G20210A (PT or rs1799963) are the genetic …

Thrombophilic gene mutations in relation to different manifestations of venous thromboembolism: a single tertiary center study

T Bezgin, C Kaymaz, Ö Akbal… - Clinical and Applied …, 2018 - journals.sagepub.com
Background: Venous thromboembolism (VTE) is a common and potentially lethal disorder
that manifests mainly as deep vein thrombosis (DVT) of the extremities or pulmonary …

Identification of genetic variants linking protein C and lipoprotein metabolism: the ARIC study (Atherosclerosis Risk in Communities)

JS Pankow, W Tang, N Pankratz, W Guan… - … , and vascular biology, 2017 - Am Heart Assoc
Objective—Previous studies have identified common genetic variants in 4 chromosomal
regions that together account for 14% to 15% of the variance in circulating levels of protein …

[HTML][HTML] Burden of rare exome sequence variants in PROC gene is associated with venous thromboembolism: a population‐based study

W Tang, MR Stimson, S Basu, SR Heckbert… - Journal of Thrombosis …, 2020 - Elsevier
Background Rare coding mutations underlying deficiencies of antithrombin and proteins C
and S contribute to familial venous thromboembolism (VTE). It is uncertain whether rare …

Thrombotic risk determined by protein C receptor (PROCR) variants among middle-aged and older adults: a population-based cohort study

E Manderstedt, C Halldén… - Thrombosis and …, 2022 - thieme-connect.com
Background The protein C (PC) anticoagulant system has a key role in maintaining
hemostatic balance. One missense (Ser219Gly) variant in the PC receptor (PROCR) was …

基于新一代测序技术的易栓症基因检测Panel 的建立及其在中国静脉血栓患者遗传背景研究中的临床应用

李蕾, 吴希, 许冠群, 梁茜, 戴菁, 武文漫, 丁秋兰… - 诊断学理论与 …, 2019 - qk.sjtu.edu.cn
目的: 研发髙效, 准确, 简单, 实用的易栓症遗传性危险因素的基因检测方法,
用于我国易栓症患者的病因诊断和治疗指导. 方法: 收集上海交通大学医学院附属瑞金医院血栓 …

Human genetics of atherothrombotic disease and its risk factors

DJ Rader - Arteriosclerosis, thrombosis, and vascular biology, 2015 - Am Heart Assoc
After carotid wire-injury, the mice deficient in endothelial Cxcr4 displayed significantly
increased neointima formation accompanied by more macrophages, reduced vascular …

The impact of the endothelial protein C receptor on thrombin generation and clot lysis

L Pepler, C Wu, DJ Dwivedi, C Wu, PY Kim… - Thrombosis Research, 2017 - Elsevier
Introduction When thrombin is bound to thrombomodulin (TM), it becomes a potent activator
of protein C (PC) and thrombin-activable fibrinolysis inhibitor (TAFI). Activation of PC is …