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Factor XII

More information in Books or onNLM PubMed
Definition: Stable blood coagulation factor activated by contact with the subendothelial surface of an injured vessel. Along with prekallikrein, it serves as the contact factor that initiates the intrinsic pathway of blood coagulation. Kallikrein activates factor XII to XIIa. Deficiency of factor XII, also called the Hageman trait, leads to increased incidence of thromboembolic disease. Mutations in the gene for factor XII that appear to increase factor XII amidolytic activity are associated with HEREDITARY ANGIOEDEMA TYPE III.     
See Also Coagulants; Hereditary Angioedema Type III
Examples Factor XIIa
Other names Hageman Factor; Coagulation Factor XII
 
SubstanceCAS Registry & nameCategoriesSourceDrugs*
factor XII Mie-1, human  0   *Factor XII Factor XII Deficiency. Thromb Haemost 2003 Jul;90(1):59-63
factor XII Locarno  0   *Factor XII. Thromb Haemost 1992 Feb 3;67(2):219-25
factor XII Bern  0   *Factor XII. Blood 1991;78(4):997
factor XII Washington D.C.  0   *Factor XII. Proc Natl Acad Sci USA 1989;86(21):8319
factor XII Toronto  0   *Factor XII. J Biochem 1988;103(4):641
factor XIIa inhibitor  0   *Blood Proteins Factor XII/antagonists & inhibitors Glycoproteins. J Biol Chem 1987;262(26):12714

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Sources: NLM Medical Subject Headings, NIH UMLS, Drugs@FDA, FDA AERS original data copyright United States Government. No endorsement implied. Last modified 6/6/2012

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