AbstractObjectivesThe physiological role of the contact system remains inconclusive. No obvious clinical complications have been observed for factor XII (FXII), prekallikrein (PK), or high molecular weight kininogen deficiencies even though the contact system in vitro is associated with coagulation, fibrinolysis, and inflammation. A global generation assay measuring the initial phase of the contact system could be a valuable tool for studies of its physiological role.Design and methodsWe investigated whether such a method could be developed using the principle of the Calibrated Automated Thrombin generation method as a template.ResultsA suitable kallikrein specific fluorogenic substrate was identified (KM=0.91mM, kcat=19s−1), and kallikrein...
High molecular weight kininogen (HMW)-kininogen, the cofactor of contact-activated blood coagulation...
Apart from tissue-type plasminogen activator (t-PA) and urokinase-type plasminogen activator (u-PA),...
by plasma protease inhibitors. This study was designed to determine the nature of these protease inh...
AbstractObjectivesThe physiological role of the contact system remains inconclusive. No obvious clin...
Blood biocompatibility of medical devices is in many ways dependent on surface characteristics and b...
BACKGROUND: The contact system (CS) proteins, factor XII and prekallikrein are thought to have roles...
Activation of the kallikrein-kinin system in hemodialysis: Role of membrane electronegativity, blood...
The activation of human plasma prekallikrein (PKK) to kallikrein (KK), induced by the contact of blo...
When blood is exposed to negatively charged surface materials such as glass, an enzymatic cascade kn...
When blood is exposed to variety of artificial surfaces and biologic substances, the plasma proteins...
Essentials During contact system activation, factor XII is progressively cleaved by plasma kallikrei...
High Mr kininogen increases the activation rate of prekallikrein by activated factor XII on a surfac...
Exposure of human blood polymorphonuclear leukocytes (PMN) to purified active plasma kallikrein resu...
I NITIATION of the intrinsic coagulation-kinin pathway requires the interaction of certain negativel...
During blood-material interaction, the enzymes factor XII fragment (factor XIIf) and kallikrein are ...
High molecular weight kininogen (HMW)-kininogen, the cofactor of contact-activated blood coagulation...
Apart from tissue-type plasminogen activator (t-PA) and urokinase-type plasminogen activator (u-PA),...
by plasma protease inhibitors. This study was designed to determine the nature of these protease inh...
AbstractObjectivesThe physiological role of the contact system remains inconclusive. No obvious clin...
Blood biocompatibility of medical devices is in many ways dependent on surface characteristics and b...
BACKGROUND: The contact system (CS) proteins, factor XII and prekallikrein are thought to have roles...
Activation of the kallikrein-kinin system in hemodialysis: Role of membrane electronegativity, blood...
The activation of human plasma prekallikrein (PKK) to kallikrein (KK), induced by the contact of blo...
When blood is exposed to negatively charged surface materials such as glass, an enzymatic cascade kn...
When blood is exposed to variety of artificial surfaces and biologic substances, the plasma proteins...
Essentials During contact system activation, factor XII is progressively cleaved by plasma kallikrei...
High Mr kininogen increases the activation rate of prekallikrein by activated factor XII on a surfac...
Exposure of human blood polymorphonuclear leukocytes (PMN) to purified active plasma kallikrein resu...
I NITIATION of the intrinsic coagulation-kinin pathway requires the interaction of certain negativel...
During blood-material interaction, the enzymes factor XII fragment (factor XIIf) and kallikrein are ...
High molecular weight kininogen (HMW)-kininogen, the cofactor of contact-activated blood coagulation...
Apart from tissue-type plasminogen activator (t-PA) and urokinase-type plasminogen activator (u-PA),...
by plasma protease inhibitors. This study was designed to determine the nature of these protease inh...