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Factor VIII
Research News and Information
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 |
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...
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...
Latest indexed articles for 'Factor VIII'
These are the very latest articles for this heading:
- Clinical problem-solving. A bloody mystery.
3 Nov 2009 - Acquired factor VIII inhibitor.
30 Oct 2009 - Structural organization of Weibel-Palade bodies revealed by cryo-EM of vitrified endothelial cells.
27 Sep 2009 - [89-year-old woman with hemorrhagic diathesis]
14 Sep 2009 - Adsorption and function of recombinant Factor VIII at the air-water interface in the presence of Tween 80.
30 Aug 2009 - A review of ERGIC-53: its structure, functions, regulation and relations with diseases.
30 Aug 2009 - Anastomosing hemangioma of the genitourinary tract: a lesion mimicking angiosarcoma.
30 Aug 2009 - Factor VIII C1 domain residues Lys 2092 and Phe 2093 contribute to membrane binding and cofactor activity.
15 Aug 2009 - Inflammation and thrombosis biomarkers and incident frailty in postmenopausal women.
11 Aug 2009 - Enhanced efficacy of recombinant FVIII in noncovalent complex with PEGylated liposome in hemophilia A mice.
2 Aug 2009 - Multimerization of peptide mimotopes for blocking of factor VIII neutralizing antibodies.
30 Jul 2009 - Stroke in sickle cell anemia: alternative etiologies.
30 Jul 2009 - Fresh frozen plasma is independently associated with a higher risk of multiple organ failure and acute respiratory distress syndrome.
30 Jul 2009 - Novel human pathological mutations. Gene symbol: F8. Disease: Hemophilia A.
30 Jul 2009 - Novel human pathological mutations. Gene symbol: F8. Disease: Haemophilia A.
30 Jul 2009 - Furtive bleeding.
30 Jul 2009 - Inhibitors of factor VIII in hemophilia.
14 Jul 2009 - Inhibitors of factor VIII in hemophilia.
14 Jul 2009 - Inhibitors of factor VIII in hemophilia.
14 Jul 2009 - Inhibitors of factor VIII in hemophilia.
14 Jul 2009
See a longer list of these articles.
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;