coagulation factor XII

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Coagulation factor XII is a protease that is essential for thrombus formation while being dispensable for hemostatic processes that terminate blood loss.

PolyP-FXII in cancer: The polyphosphate/factor-XII pathway in cancer-driven thrombosis and tumor growth

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.

Association of FXII 5'UTR 46C>T polymorphism with FXII activity and risk of thrombotic disease/FXII 5'UTR 46C>T polimorfizmi ile FXII aktivitesi ve trombotik hastalik riskinin iliskisi

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.

In some families, individuals with HAE with normal C1-INH function have a gain-of-function mutation in coagulation factor XII that may result in enhanced generation of bradykinin.

A girl with severe hand swelling and abdominal cramps

Blood coagulation factor XII (FXII; Hageman factor) is a serine protease.

Rapid factor XII (46C [right arrow] T) genotyping by fluorescence resonance energy transfer in patients with coronary artery disease or thrombophilia

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