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Interconnections between the coagulation process and complement cascade have been reported by many authors [ 53, 54].
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The coagulation process destabilizes colloidal particles by adding a coagulant and results in the sedimentation process (Shammas 2004).
For both PCA and CCA, the coagulation process is completed when the maximum distance between any pair of monomers of the aggregate exceeds a certain upper limit.
Moreover, because whole blood is analysed, TEG takes account of interactions between all blood components (platelets, coagulation factors, leucocytes etc). in the coagulation process.
Fibrinogen is an important coagulation factor, acting not only as the precursor of fibrin, the end product of the coagulation process [ 6, 27], but also as a key ligand between activated platelets [ 28].
Such cross-activation serves to amplify the coagulation process.
Congenital disorders of the coagulation process usually become manifest during infancy or early childhood.
This might have increased the concentration of active coagulation polymer in the extract, which improved the coagulation process.
The coagulation process was monitored using near infrared spectrometry, small amplitude oscillatory rheometry and visual coagulation indexes.
Fibrinogen is one of the most important proteins in the coagulation process.
The main objective of this work was to optimize the coagulation process by BBD of RSM.
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