血管性血友病因子
ADAMTS13号
止血
血管性血友病
狭窄
血栓形成
医学
内科学
血栓性血小板减少性紫癜
心脏病学
血小板
出处
期刊:Asaio Journal
[Lippincott Williams & Wilkins]
日期:2012-02-25
卷期号:58 (2): 163-169
被引量:33
标识
DOI:10.1097/mat.0b013e31824363e7
摘要
von Willebrand factor (VWF), an adhesive glycoprotein whose deficiency is best known for causing bleeding in patients with von Willebrand disease (VWD), is a complex molecule with a myriad of mysterious properties including its dependence on shear stress for adhesive functions. The discovery of ADAMTS13 has provided a critical impetus for understanding the regulation of VWF activity by shear stress. This communication reviews the current knowledge in VWF homeostasis and illustrates how this knowledge may help understand the changes affecting patients with various conditions including thrombotic thrombocytopenic purpura, VWD, hemolytic uremic syndrome, aortic stenosis, and ventricular assist devices.
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