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  2. List of human blood components - Wikipedia

    en.wikipedia.org/wiki/List_of_human_blood_components

    Antihemophilic factor: 1 × 10 −7: Christmas factor: 4 × 10 −6: Stuart factor: 5 × 10 −6: Plasma thrmb. anteced. 4 × 10 −6: Hageman factor: 2.9 × 10 −5: Fibrin-stabilizing factor: 1 × 10 −5: Fibrin split products <1 × 10 −5: Fletcher factor: 5 × 10 −5: Fitzgerald factor: 7 × 10 −5: von Willebrand factor: 7 × 10 −6 ...

  3. Coagulation - Wikipedia

    en.wikipedia.org/wiki/Coagulation

    The coagulation factors are generally enzymes called serine proteases, which act by cleaving downstream proteins. The exceptions are tissue factor, FV, FVIII, FXIII. [28] Tissue factor, FV and FVIII are glycoproteins, and Factor XIII is a transglutaminase. [27] The coagulation factors circulate as inactive zymogens. The coagulation cascade is ...

  4. Contact activation system - Wikipedia

    en.wikipedia.org/wiki/Contact_activation_system

    FXIIa's cleavage of FXI initiates coagulation. In the contact activation system or CAS, three proteins in the blood, factor XII (FXII), prekallikrein (PK) and high molecular weight kininogen (HK), bind to a surface and cause blood coagulation and inflammation. FXII and PK are proteases and HK is a non-enzymatic co-factor

  5. Hemostasis - Wikipedia

    en.wikipedia.org/wiki/Hemostasis

    The third and last step is called coagulation or blood clotting. Coagulation reinforces the platelet plug with fibrin threads that act as a "molecular glue". [3] Platelets are a large factor in the hemostatic process. They allow for the creation of the "platelet plug" that forms almost directly after a blood vessel has been ruptured.

  6. Tenase - Wikipedia

    en.wikipedia.org/wiki/Tenase

    In coagulation, the coagulation factor X can be activated into factor Xa in two ways: either extrinsically or intrinsically. The activating complexes are together called tenase . Tenase is a blend word of "ten" and the suffix "-ase", which means, that the complex activates its substrate (inactive factor X) by cleaving it.

  7. Factor XIII - Wikipedia

    en.wikipedia.org/wiki/Factor_XIII

    Factor XIII, or fibrin stabilizing factor, is a plasma protein and zymogen. It is activated by thrombin to factor XIIIa which crosslinks fibrin in coagulation. Deficiency of XIII worsens clot stability and increases bleeding tendency. [1] Human XIII is a heterotetramer. It consists of 2 enzymatic A peptides and 2 non-enzymatic B peptides.

  8. Thrombosis - Wikipedia

    en.wikipedia.org/wiki/Thrombosis

    Thrombosis (from Ancient Greek θρόμβωσις (thrómbōsis) 'clotting') is the formation of a blood clot inside a blood vessel, obstructing the flow of blood through the circulatory system. When a blood vessel (a vein or an artery) is injured, the body uses platelets (thrombocytes) and fibrin to form a blood clot to prevent blood loss ...

  9. Category:Coagulation system - Wikipedia

    en.wikipedia.org/wiki/Category:Coagulation_system

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