نتایج جستجو برای: fxiii 100 gt polymorphism

تعداد نتایج: 586334  

Farsinejad, Alireza, Ala, Fereydoun , Faranoush, Mohammad, Kazemzadeh, Shima, Mohammadi, Rezvan , Shadkam Farokhi, Fatemeh, Shafiian, Alireza,

Background: The most common polymorphisms identified in the Methylenetetrahydrofolate reductase (MTHFR) gene, C677T and A1298C lead to defective activity of this enzyme and increase the risk of venous and arterial thrombosis. There are limited investigations regarding the effects of thrombogenic polymorphisms on the clinical phenotypes of rare hereditary hemorrhagic disorders like Glanzmann's t...

2013
José Hinz Daniel Schöndorf Christian Bireta Christina Lipke Onnen Moerer Ingo Bergmann Christoph Herman Wiese Ashham Mansur Hanna Schotola Anton Sabashnikov Michael Quintel Friedrich Albert Schoendube Aron Frederik Popov

BACKGROUND The eNOS 894G/T polymorphism (GG, GT, and TT) is associated with cardiovascular mortality and may influence cardiovascular diseases as a genetic risk factor. Moreover, this polymorphism has an impact on intraoperative hemodynamics during cardiac surgery with cardiopulmonary bypass (CPB). In this study, we analyzed the influence of this gene polymorphism on early clinical outcome in p...

2000
Alexis Elbaz Odette Poirier Sandrine Canaple François Chédru François Cambien

Factor XIII catalyzes the formation of covalent bounds between fibrin monomers, thus stabilizing the fibrin clot and increasing its resistance to fibrinolysis. The frequency of a frequent Val34Leu polymorphism in the FXIII A-subunit gene has been shown to be lower in patients with myocardial infarction or venous thrombosis than in controls, whereas it was higher in patients with hemorrhagic str...

Journal: :American journal of epidemiology 2009
Fangfang Song Xiangyang Li Muxun Zhang Ping Yao Nianhong Yang Xiufa Sun Frank B Hu Liegang Liu

The authors aimed to determine whether 2 functional polymorphisms in the heme oxygenase-1 (HO-1) gene promoter are associated with type 2 diabetes mellitus (T2DM). A Chinese case-control study involving 1,103 newly diagnosed T2DM patients, 371 patients with impaired glucose regulation (IGR), and 1,615 controls was performed (December 2004-December 2007). A (GT)(n) microsatellite polymorphism an...

Journal: :Blood 2000
A Elbaz O Poirier S Canaple F Chédru F Cambien P Amarenco

Factor XIII catalyzes the formation of covalent bounds between fibrin monomers, thus stabilizing the fibrin clot and increasing its resistance to fibrinolysis. The frequency of a frequent Val34Leu polymorphism in the FXIII A-subunit gene has been shown to be lower in patients with myocardial infarction or venous thrombosis than in controls, whereas it was higher in patients with hemorrhagic str...

Journal: :Pathophysiology of haemostasis and thrombosis 2003
Zsuzsanna Bereczky Eva Katona László Muszbek

Factor XIII (FXIII) is a zymogen that is converted into an active transglutaminase (FXIIIa) by the concerted action of thrombin and Ca2+. Its main task is to crosslink alpha-, and gamma-chains of fibrin and alpha2-plasmin inhibitor to fibrin. By this way FXIIIa strengthens fibrin and protects it from the prompt elimination by fibrinolytic system.The changes of FXIII level in thrombotic diseases...

2009
Éva Ajzner Ágota Schlammadinger Adrienne Kerényi Zsuzsanna Bereczky Éva Katona Gizella Haramura Zoltán Boda László Muszbek

Acquired factor XIII (FXIII) deficiency due to autoantibody against FXIII is a very rare severe hemorrhagic diathesis. Antibodies directed against theAsubunit of FXIII, which interfere with different functions of FXIII, have been described. Here, for the first time, we report an autoantibody against the B subunit of FXIII (FXIII-B) that caused lifethreatening bleeding in a patient with systemic...

Journal: :Journal of the American College of Cardiology 2005
Francisco Marín Rocío González-Conejero Kaeng W Lee Javier Corral Vanessa Roldán Francisca López Francisco Sogorb Juan Caturla Gregory Y H Lip Vicente Vicente

OBJECTIVES The aim of this study was to evaluate the pharmacogenetic role of the factor XIII (FXIII) valine 34 leucine (Val34Leu) polymorphism in the fibrinolytic therapy of acute myocardial infarction (MI). BACKGROUND Fibrinolytic therapy is an established treatment for acute MI, but up to 40% of treated patients do not achieve optimal tissue reperfusion. The FXIII Val34Leu polymorphism is o...

Journal: :QJM : monthly journal of the Association of Physicians 1999
H P Kohler P J Grant

Blood coagulation factor XIII (also called fibrinplasma as a tetramer (A 2 B 2 ).12 All A-subunit molecules in plasma are in complex with the B-subunit (carrier stabilizing factor1) plays an important role in clot stabilization by crosslinking fibrin chains.2 Factor XIII protein) at a concentration of approximately 21 mg/ml, whereas the B-subunit is present in both free and (FXIII) was discover...

Journal: :Thrombosis and haemostasis 2007
Verena Schroeder Jean-Marc Vuissoz Amedeo Caflisch Hans P Kohler

The first step of coagulation factor XIII (FXIII) activation involves cleavage of the FXIII activation peptide (FXIII-AP) by thrombin. However, it is not known whether the FXIII-AP is released into plasma upon cleavage or remains attached to activated FXIII. The aim of the present work was to study the structure of free FXIII-AP, develop an assay for FXIII-AP determination in human plasma, and ...

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