نتایج جستجو برای: von willebrand factor

تعداد نتایج: 931957  

Journal: :Lymphology 1996
A Di Nucci C Marchetti S Serafini F Piovella

P-selectin (PADGEM, GMP-140, CD62) is an integral membrane protein specific to alpha granules of platelets and Weibel-Palade bodies of blood vascular endothelial cells. The presence in lymphatic endothelial cells of numerous Weibel-Palade bodies and their positivity to immunocytochemical reaction for von Willebrand factor have previously been characterized and described. Because von Willebrand ...

Journal: :Haemophilia : the official journal of the World Federation of Hemophilia 1991
D Ginsburg

von Willebrand disease is the most common inherited bleeding disorder in humans, with the general population prevalence estimated to be as high as 1% in some studies. This condition exhibits extensive heterogeneity with over 20 distinct subtypes distinguished based on subtle clinical and laboratory differences in presentation. Recent research laboratory advances have shed considerable new light...

2016
Xin Wang Francesca M. Chappell Maria Valdes Hernandez Gordon Lowe Ann Rumley Kirsten Shuler Fergus Doubal Joanna M. Wardlaw

BACKGROUND AND OBJECTIVE Recent studies suggest perivascular spaces are a marker of small vessel disease, blood-brain barrier permeability, and inflammation, but little is known about their risk factors and associations with peripheral blood markers. MATERIALS AND METHODS In prospectively recruited patients with recent minor ischemic stroke, we investigated the influence of age, sex, hyperten...

2017
P. Baud A. Tobler B. Lämmle L. Alberio

We present a woman (age: 57 years) with an excessive bleeding episode under acetylsalicylic acid after bone marrow puncture due to an acquired von Willebrand syndrome (avWS) in the context of a myeloproliferative disorder. The laboratory features showed a high platelet concentration and a qualitative defect of von Willebrand factor (vWF) with a low normal vWF ristocetin cofactor activity, a nor...

Journal: :Mayo Clinic proceedings 2006
Rajiv K Pruthi

von Willebrand disease (vWD) is the most commonly diagnosed congenital bleeding disorder. The laboratory diagnosis of type 2 variants and type 3 vWD is reasonably well defined, and characterization of the von Willebrand factor (vWF) gene has facilitated definition of their molecular basis. However, for type 1 vWD, the laboratory diagnosis poses a diagnostic dilemma, and knowledge of its molecul...

Journal: :European heart journal 2002
P H Whincup J Danesh M Walker L Lennon A Thomson P Appleby A Rumley G D O Lowe

AIMS To determine whether circulating von Willebrand factor concentrations are prospectively related to risk of coronary heart disease in the general population. METHODS AND RESULTS We measured baseline von Willebrand factor values in the stored serum samples of 625 men with major coronary events and in 1266 controls 'nested' in a prospective study of 5661 men aged 40-59 years, recruited from...

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 ...

2010
Renske G. Wieberdink Albert Hofman Jacqueline C.M. Witteman Frank W.G. Leebeek Monique M.B. Breteler

Background and Purpose—Many studies have investigated the role of plasma von Willebrand factor level in coronary heart disease, but few have investigated its role in stroke. The aim of this study was to determine if von Willebrand factor levels are associated with the risk of stroke. Methods—The study was part of the Rotterdam Study, a large population-based cohort study among subjects aged 55 ...

Journal: :Journal of cell science 2003
Matthew J Hannah Alistair N Hume Monica Arribas Ross Williams Lindsay J Hewlett Miguel C Seabra Daniel F Cutler

The identification of organelles is crucial for efficient cellular function, yet the basic underlying mechanisms by which this might occur have not been established. One group of proteins likely to be central to organelle identity is the Rab family of small GTPases. We have thus investigated Rab recruitment to membranes using endothelial cells as a model system. We report that Weibel-Palade bod...

Journal: :Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2012
Nathalie C Péquériaux Rob Fijnheer Eugenie F Gemen Arjan D Barendrecht Friedo W Dekker Raymond T Krediet Jaap J Beutler Elisabeth W Boeschoten Mark Roest

BACKGROUND Traditional cardiovascular risk factors do not explain the high incidence of cardiovascular mortality and morbidity in patients with end-stage renal disease. A prothrombotic state could accelerate the process of vascular disease in these patients. METHODS In this study, four platelet activation markers (NAP-2, P-selectin, GP1b and RANTES) and two endothelial cell activation markers...

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