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Num Mark Subjects (1-10 of 10) Year Entries
10 Found
1 Factor XI. : The physiology and pathology of coagulation factor XI / David Gailani  2007 1
2 Factor XI -- antagonists & inhibitors. : Inhibitors in patients with haemophilia / edited by E.C. Rodriguez-Merchan, C.A. Lee  2002 1
3  

Factor XI, Coagulation -- See Factor XI


Stable blood coagulation factor involved in the intrinsic pathway. The activated form XIa activates factor IX to IXa. Deficiency of factor XI is often called hemophilia C
  1
4  

Factor XI Deficiencies -- See Factor XI Deficiency


A hereditary deficiency of blood coagulation factor XI (also known as plasma thromboplastin antecedent or PTA or antihemophilic factor C) resulting in a systemic blood-clotting defect called hemophilia C or Rosenthal's syndrome, that may resemble classical hemophilia
  1
5  

Factor XI Deficiency -- See Also Factor XI


Stable blood coagulation factor involved in the intrinsic pathway. The activated form XIa activates factor IX to IXa. Deficiency of factor XI is often called hemophilia C
  1
6 Factor XI Deficiency. : The physiology and pathology of coagulation factor XI / David Gailani  2007 1
7 Factor XI -- physiology. : The physiology and pathology of coagulation factor XI / David Gailani  2007 1
8 Factor XIII. : Fibrinogen and factor XIII / John W. Weisel  2007 1
9  

Factor XIII, Coagulation -- See Factor XIII


A fibrin-stabilizing plasma enzyme (TRANSGLUTAMINASES) that is activated by THROMBIN and CALCIUM to form FACTOR XIIIA. It is important for stabilizing the formation of the fibrin polymer (clot) which culminates the coagulation cascade
  1
10  

Factor XIII Transamidase -- See Factor XIII


A fibrin-stabilizing plasma enzyme (TRANSGLUTAMINASES) that is activated by THROMBIN and CALCIUM to form FACTOR XIIIA. It is important for stabilizing the formation of the fibrin polymer (clot) which culminates the coagulation cascade
  1
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