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Factor VIII
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Definition of 'Factor VIII'

Blood-coagulation factor VIII. Antihemophilic factor that is part of the factor VIII/von Willebrand factor complex. Factor VIII is produced in the liver and acts in the intrinsic pathway of blood coagulation. It serves as a cofactor in factor X activation and this action is markedly enhanced by small amounts of thrombin.

Common names: Factor VIII; Thromboplastinogen; Coagulation Factor VIII; Factor VIII, Coagulation; VIII, Coagulation Factor; Antihemophilic Factor; Blood Coagulation Factor VIII; Factor VIII Procoagulant Activity; Factor VIII-Heavy Chain; Factor VIII Heavy Chain; Factor VIIIC; F VIII-C; F VIII C; Humate-P

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Monday, November 23, 2009

Structural organization of Weibel-Palade bodies revealed by cryo-EM of vitrified endothelial cells.

27 Sep 2009 In endothelial cells, the multifunctional blood glycoprotein von Willebrand Factor (VWF) is stored for rapid exocytic release in specialized secretory granules called Weibel-Palade bodies (WPBs). Electron cryomicroscopy at the thin periphery of ... Read more...


Adsorption and function of recombinant Factor VIII at the air-water interface in the presence of Tween 80.

30 Aug 2009 The air-water surface tension kinetic and steady state behavior exhibited by a recombinant Factor VIII were recorded in the presence of the surfactant Tween 80. The rate of surface tension decrease was determined to be greater for rFVIII-Tween ... Read more...


A review of ERGIC-53: its structure, functions, regulation and relations with diseases.

30 Aug 2009 ERGIC-53 is a type I transmembrane protein. It includes an N-terminal signal sequence, a carbohydrate recognition domain, which is calcium-dependent and pH-sensitive, a stalk region, a transmembrane domain, and a short cytoplasmic domain; ERGIC-53 ... Read more...

 

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Technical information about 'Factor VIII'

Definition: Blood-coagulation factor VIII. Antihemophilic factor that is part of the factor VIII/von Willebrand factor complex. Factor VIII is produced in the liver and acts in the intrinsic pathway of blood coagulation. It serves as a cofactor in factor X activation and this action is markedly enhanced by small amounts of thrombin.

Chemical name: Blood-coagulation factor VIII, complex

Registry Number: 9001-27-8

Descriptor UI: D005169

Alternative terms: Factor VIII; Thromboplastinogen; Coagulation Factor VIII; Factor VIII, Coagulation; VIII, Coagulation Factor; Antihemophilic Factor; Blood Coagulation Factor VIII; Factor VIII Procoagulant Activity; Factor VIII-Heavy Chain; Factor VIII Heavy Chain; Factor VIIIC; F VIII-C; F VIII C; Humate-P; Humate P; HumateP; Hyatt-C; Hyatt C; HyattC; Hyate-C; Hyate C; HyateC; Monoclate; Factor VIII Coagulant Antigen; Factor VIII Clotting Antigen; Hemofil; Hemofil M; Hemophil; Hemofil HM;

Allowable Qualifiers: administration & dosage; adverse effects; analysis; antagonists & inhibitors; biosynthesis; cerebrospinal fluid; chemical synthesis; classification; diagnostic use; drug effects; economics; genetics; history; immunology; isolation & purification; metabolism; pharmacokinetics; pharmacology; physiology; poisoning; radiation effects; secretion; standards; supply & distribution; therapeutic use; toxicity; ultrastructure; urine; chemistry; contraindications; agonists;

Pharmacological Action: Coagulants;

Tree Number: D12.776.124.125.350; D23.119.350;

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