نتایج جستجو برای: platelet von willebrand factor

تعداد نتایج: 1021349  

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...

Journal: :Blood 1996
C P Hayward G E Rivard W H Kane J Drouin S Zheng J C Moore J G Kelton

Multimerin is a massive soluble, multimeric protein found in platelets and endothelial cells. Recent studies identified multimerin as a specific coagulation factor V binding protein, complexed with platelet, but not plasma, factor V. These findings led us to investigate individuals with inherited factor V deficiencies for possible multimerin abnormalities. Platelet proteins were evaluated using...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1995
T C Nichols C M Samama D A Bellinger J Roussi R L Reddick M Bonneau M S Read O Bailliart G G Koch M Vaiman

von Willebrand factor (vWF) is essential for the induction of occlusive thrombosis in stenosed and injured pig arteries and for normal hemostasis. To separate the relative contribution of plasma and platelet vWF to arterial thrombosis, we produced chimeric normal and von Willebrand disease pigs by crossed bone marrow transplantation; von Willebrand disease (vWD) pigs were engrafted with normal ...

Journal: :Blood 1983
B S Coller E I Peerschke L E Scudder C A Sullivan

A murine monoclonal antibody directed at or near a platelet membrane receptor for the von Willebrand factor was produced by the hybridoma technique. Purified F(ab')2 fragments and/or intact antibody completely blocked the agglutination of platelets induced by both ristocetin and bovine von Willebrand factor and the binding of von Willebrand factor antigen to platelets. The antibody also decreas...

2013
Neetu Grover Vincent Boama Munazzah Rifat Chou

BACKGROUND Pseudo (platelet-type)-von Willebrand disease is a rare autosomal dominant bleeding disorder caused by an abnormal function of the glycoprotein lb protein; the receptor for von Willebrand factor. This leads to an increased removal of VWF multimers from the circulation as well as platelets and this results in a bleeding diathesis. Worldwide, less than 50 patients are reported with pla...

Journal: :Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2017
Dan Secor Scott Swarbreck Christopher G Ellis Michael D Sharpe Qingping Feng Karel Tyml

Plugging of the capillary bed can lead to organ failure and mortality in sepsis. We have reported that intravenous ascorbate injection reduces platelet adhesion to the capillary wall and capillary plugging in septic mice. Both platelet adhesion and capillary plugging require P-selectin, a key adhesion molecule. To elucidate the beneficial effect of ascorbate, we hypothesized that ascorbate redu...

Journal: :Arteriosclerosis, thrombosis, and vascular biology 2013
Eliane Berrou Frédéric Adam Marilyne Lebret Patricia Fergelot Alexandre Kauskot Isabelle Coupry Martine Jandrot-Perrus Alan Nurden Rémi Favier Jean-Philippe Rosa Cyril Goizet Paquita Nurden Marijke Bryckaert

OBJECTIVE We examined platelet functions in 4 unrelated patients with filaminopathy A caused by dominant mutations of the X-linked filamin A (FLNA) gene. METHODS AND RESULTS Patients P1, P2, and P4 exhibited periventricular nodular heterotopia, heterozygozity for truncating FLNA mutations, and thrombocytopenia (except P2). P3 exhibited isolated thrombocytopenia and heterozygozity for a p.Glu1...

Journal: :Arteriosclerosis, thrombosis, and vascular biology 2014
Adam Corken Susan Russell Judith Dent Steven R Post Jerry Ware

OBJECTIVE The platelet glycoprotein Ib-IX (GP Ib-IX) receptor is a well-characterized adhesion receptor supporting hemostasis and thrombosis via interactions with von Willebrand factor. We examine the GP Ib-IX/von Willebrand factor axis in murine polymicrobial sepsis, as modeled by cecal ligation and puncture (CLP). APPROACH AND RESULTS Genetic absence of the GP Ib-IX ligand, von Willebrand f...

Journal: :Stroke 2014
Andrew M Naidech Matthew B Maas Kimberly E Levasseur-Franklin Eric M Liotta James C Guth Micheal Berman Joshua M Rosenow Paul F Lindholm Bernard R Bendok Shyam Prabhakaran Richard A Bernstein Hau C Kwaan

BACKGROUND AND PURPOSE Minimizing hematoma growth in high-risk patients is an attractive strategy to improve outcomes after intracerebral hemorrhage. We tested the hypothesis that desmopressin (DDAVP), which improves hemostasis through the release of von Willebrand factor, improves platelet activity after intracerebral hemorrhage. METHODS Patients with reduced platelet activity on point-of-ca...

Journal: :Blood 1990
J D Sweeney E K Novak M Reddington K H Takeuchi R T Swank

Mice of the RIIIS/J inbred strain have prolonged bleeding times (greater than 15 minutes) after experimental injury when compared with normal C57BL/6J mice (1.8 minutes) and other strains of mice. The prolonged bleeding time was accompanied by normal platelet counts. Platelet aggregation with collagen and agglutination with ristocetin were not significantly altered in RIIIS/J mice. Also, platel...

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