نتایج جستجو برای: gpib

تعداد نتایج: 652  

Journal: :Journal of cardiovascular pharmacology 2001
G Amoroso A J van Boven D J van Veldhuisen R A Tio C P Baljé-Volkers A S Petronio W van Oeveren

Platelet deposition and aggregation are the major determinants of acute thrombosis in coronary stents. We aimed to compare the antiplatelet efficacy of different treatments--glycoprotein (Gp) IIb/IIIa inhibitors and conventional antiaggregants--in an experimental model for stenting. Blood samples were obtained from patients with coronary artery disease (n = 15) and healthy volunteers (n = 8) an...

Journal: :Blood 1999
S Béguin R Kumar I Keularts U Seligsohn B S Coller H C Hemker

Thrombin generation in platelet-rich plasma (PRP) involves complex interactions between platelets and coagulation proteins. We previously reported that the addition of fibrin to PRP enhances tissue-factor initiated thrombin generation by approximately 40%, and the current studies were designed to assess the mechanism(s) underlying thrombin generation in the absence and presence of fibrin. Block...

Journal: :Journal of thrombosis and haemostasis : JTH 2011
Y Buyukasik

BACKGROUND Severe thrombocytopenia is a major risk factor for hemorrhage, but platelet function and bleeding risk at low platelet counts are poorly understood, because of the limitations of platelet function testing at very low platelet counts. OBJECTIVES To examine and compare platelet function in severely thrombocytopenic patients with acute myeloid leukemia (AML) or myelodysplasia (MDS) wi...

Journal: :Blood 2000
N Ajzenberg A S Ribba G Rastegar-Lari D Meyer D Baruch

The aim was to better understand the function of von Willebrand factor (vWF) A1 domain in shear-induced platelet aggregation (SIPA), at low (200) and high shear rate (4000 seconds(-1)) generated by a Couette viscometer. We report on 9 fully multimerized recombinant vWFs (rvWFs) expressing type 2M or type 2B von Willebrand disease (vWD) mutations, characterized respectively by a decreased or inc...

Journal: :Blood 1991
A S Ribba J M Lavergne B R Bahnak A Derlon G Piétu D Meyer

von Willebrand disease (vWD) type IIB is characterized by an increased reactivity of von Willebrand factor (vWF) with platelets and a lack of large multimers. Exon 28 of the vWF gene encodes for functional domains involved in the binding of vWF to GPIb, and it is presumed that the defects in type IIB vWD lie within or adjacent to these functional domains. We screened overlapping DNA fragments g...

Journal: :Blood 2008
Utpal P Davé

on the activated platelets can bind PSGL-1, strengthening the association between the activated neutrophil microparticle and the platelets. It has been previously established that GPIb directly binds activated leukocyte Mac-1,5 as well as P-selectin expressed on activated platelets/endothelial cells,3,6 enabling GPIb -mediated plateletleukocyte-endothelial cell crosstalk; for example, platelets...

Journal: :Circulation 2007
Christoph Kleinschnitz Miroslava Pozgajova Mirko Pham Martin Bendszus Bernhard Nieswandt Guido Stoll

BACKGROUND Ischemic stroke is a frequent and serious disease with limited treatment options. Platelets can adhere to hypoxic cerebral endothelial cells by binding of their glycoprotein (GP) Ib receptor to von Willebrand factor. Exposure of subendothelial matrix proteins further facilitates firm attachment of platelets to the vessel wall by binding of collagen to their GPVI receptor. In the pres...

ژورنال: :مجله علمی دانشگاه علوم پزشکی قزوین 0
کریم شمس اسنجان k. shams asanjan قزوین، دانشگاه علوم پزشکی، دانشکده بهداشت و پیراپزشکی، گروه علوم آزمایشگاهی

چکیده زمینه : سندرم برنارد سولیر بیماری نادری است که کلید تشخیصی آن اثبات عدم حضور کمپلکس غشایی پلاکت ib/ix با استفاده از روش تجمع سنجی پلاکتی است. هدف : مطالعه به منظور بررسی امکان استفاده از روش فلوسیتومتری پلاکت ها در تشخیص بیماری برنارد سولیر انجام شد. مواد و روش ها : در سال 1379 در سازمان انتقال خون ایران 15 بیمار مشکوک به سندرم برنارد سولیر به عنوان گروه مورد و بیست فرد سالم به عنوان گروه...

Journal: :Blood 1996
J W Semple Y Milev D Cosgrave M Mody A Hornstein V Blanchette J Freedman

Patients with both acute and chronic autoimmune thrombocytopenic purpura (AITP) have in vitro lymphocyte defects in the form of platelet-stimulated proliferation and cytokine secretion. A blinded study was performed to determine if these defects are related to serum cytokine levels and/or platelet antigen expression. Compared with controls, 53% of children with chronic AITP, but only 9% of thos...

Journal: :Blood 1993
B R Alevriadou J L Moake N A Turner Z M Ruggeri B J Folie M D Phillips A B Schreiber M E Hrinda L V McIntire

Two likely mechanisms for the initiation of arterial platelet thrombus formation under conditions of elevated fluid shear stresses are: (1) excessive adhesion and aggregation of platelets from rapidly flowing blood onto the exposed sub-endothelium of injured, atherosclerotic arteries; or (2) direct, fluid shear stress-induced aggregation of platelets in constricted arteries with intact endothel...

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