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The C46T polymorphism of the coagulation factor XII gene and idiopathic recurrent miscarriage.
Role of coagulation factor XII in unexplained recurrent abortions in the Greek population.
Coagulation factor XII is a protease that is essential for thrombus formation while being dispensable for hemostatic processes that terminate blood loss.
Role of surface in surface-dependent activation of Hageman factor (blood coagulation Factor XII).
A common genetic polymorphism (46 C to T substitution) in the 5'-untranslated region of the coagulation factor XII gene is associated with low transition efficiency and decrease in plasma FXII level.
A common C-T polymorphism at nt 46 in the promoter region of coagulation factor XII is associated with decreased factor XII activity.
Coagulation factor XII activity, activated factor XII, distribution of factor XII C46T gene polymorphism and coronary risk.
This type of HAE may be due to increased activity of coagulation factor XII (6).
C1-INH is a major inhibitor of kallikrein and coagulation factor XII (Fig.
Blood coagulation factor XII (FXII; Hageman factor) is a serine protease.
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