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10.1016/j.blre.2020.100733

http://scihub22266oqcxt.onion/10.1016/j.blre.2020.100733
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32682574!7354275!32682574
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suck abstract from ncbi

pmid32682574      Blood+Rev 2021 ; 46 (ä): 100733
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  • Interplay between platelets and coagulation #MMPMID32682574
  • Sang Y; Roest M; de Laat B; de Groot PG; Huskens D
  • Blood Rev 2021[Mar]; 46 (ä): 100733 PMID32682574show ga
  • Haemostasis stops bleeding at the site of vascular injury and maintains the integrity of blood vessels through clot formation. This regulated physiological process consists of complex interactions between endothelial cells, platelets, von Willebrand factor and coagulation factors. Haemostasis is initiated by a damaged vessel wall, followed with a rapid adhesion, activation and aggregation of platelets to the exposed subendothelial extracellular matrix. At the same time, coagulation factors aggregate on the procoagulant surface of activated platelets to consolidate the platelet plug by forming a mesh of cross-linked fibrin. Platelets and coagulation mutually influence each other and there are strong indications that, thanks to the interplay between platelets and coagulation, haemostasis is far more effective than the two processes separately. Clinically this is relevant because impaired interaction between platelets and coagulation may result in bleeding complications, while excessive platelet-coagulation interaction induces a high thrombotic risk. In this review, platelets, coagulation factors and the complex interaction between them will be discussed in detail.
  • |*Blood Coagulation[MESH]
  • |*Hemostasis[MESH]
  • |Blood Coagulation Disorders/blood/diagnosis/etiology[MESH]
  • |Blood Coagulation Factors/metabolism[MESH]
  • |Blood Coagulation Tests[MESH]
  • |Blood Platelets/*physiology[MESH]
  • |Disease Susceptibility[MESH]
  • |Humans[MESH]
  • |Platelet Activation[MESH]
  • |Platelet Aggregation[MESH]
  • |Platelet Membrane Glycoproteins/metabolism[MESH]


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