نتایج جستجو برای: human factor viii light chain

تعداد نتایج: 2850410  

Journal: :iranian journal of blood and cancer 0
mohsin sh jaffar j hussain sh suhail sh ikram ullah m amjad s

background: factor viii administration to hemophilia a patients results in an immune response (inhibitor formation) which significantly complicates the therapy. the present study was performed to determine the prevalence of inhibitor development in hemophilia a patients receiving recombinant factor viii therapy. materials and methods: this was an observational descriptive study. clotting factor...

Journal: :Blood 1985
V T Turitto H J Weiss T S Zimmerman I I Sussman

The present studies were undertaken to determine whether factor VIII/von Willebrand factor (vWF) present in the vessel wall (in addition to that in plasma) may mediate the attachment of platelets to subendothelium. Subendothelium from everted rabbit aorta was exposed to human citrated blood flowing through an annular perfusion chamber at 40 mL/min (wall shear rate of 2,600 s-1 for five minutes)...

Journal: :The Journal of Experimental Medicine 1975
R L Nachman E A Jaffe

Subcellular membrane and granule fractions derived from human platelets contain factor VIIII antigen and von Willebrand factor activity but not factor VII procoagulant activity. Circulating platelets constitute a significant reservoir of plasma factor VIII antigen, containing approximately 15% of the amount of factor VIII antigen present in platelet-poor plasma. The antibiotic ristocetin, which...

Journal: :The Journal of biological chemistry 1991
R J Wise A J Dorner M Krane D D Pittman R J Kaufman

von Willebrand factor (vWF) is a multimeric glycoprotein that promotes platelet aggregation and stabilizes coagulation factor VIII in the plasma. vWF is also required for the stable accumulation of recombinant factor VIII secreted from cells in a heterologous expression system. In this report, we show that vWF can promote the in vitro reconstitution of factor VIII activity from dissociated heav...

Journal: :Blood 2000
H P Schwarz P J Lenting B Binder J Mihaly C Denis F Dorner P L Turecek

Factor VIII is tightly noncovalently linked to von Willebrand factor (vWF) in plasma with a stoichiometry of 1:50, and vWF deficiency results in secondary factor VIII deficiency, with accelerated clearance of factor VIII from the circulation. We used a murine model of severe von Willebrand disease (vWF knockout mice) to study the effect of a recombinant vWF/pro-vWF preparation (rpvWF) on factor...

ژورنال: پژوهش در پزشکی 2006
دکتر امیر هوشنگ محمد علیزاده, , دکتر سید محسن موسوی, , دکتر فرحناز فلاحیان, , دکتر محمد رضا زالی, , دکتر محمد عباسی, , دکتر مهرداد حاجیلویی, , دکتر میترا رنجبر, , دکترمهدی رضازاده, ,

Abstract: Background: Hemophilia is a x-linked deficiency of factor VIII. The aim of the present study was to determine the frequencies of hepatitis B and C infections, markers of inflammation and liver function tests and also to assess the possible association between factor VIII inhibitor and hepatitis B and C infections in hemophiliacs of Hamedan Province of Iran. Materials and methods: Si...

Journal: :medical journal of islamic republic of iran 0
t zandieh from the iranian blood fractionation and research company, tehran m farhadi the iranian blood transfusion service, tehran m shahr-abadi the virology lab, rasool akram hospital, tehran, i.r. iran. h lotfi from the iranian blood fractionation and research company, tehran

we prepared a highly purified and relatively heat stable form of factor viii which contained 25 units per ml (u/ml) activity using peg-4000 and developed an effective and new manufacturing process. heat treatment was performed at 80°c for 72 hrs in the presence of different stabilizers. in our studies, we used different organic solvents as preservatives to maintain factor viii activity, since f...

Journal: :Blood 1976
B N Bouma J A van Mourik S de Graaf J M Hordijk-Hos J J Sixma

Since dialysis of human factor VIII against buffers of low ionic strength yielded two distinct components, and since the factor VIII fraction isolated from normal plasma showed von Willebrand factor activity as defined by the corrective effect on abnormal platelet retention and ristocetin aggregation in von Willebrand's disease, the present studies were performed to determine if the correcting ...

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