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Showing 1 to 20 of 51 for “"vWF"”.

  1. Understanding the Role of von Willebrand Factor (VWF) in Angiogenesis and Angiodysplasia

    von Willebrand factor (VWF) is a large multimeric glycoprotein essential for hemostasis, mediating platelet adhesion to sites of vascular injury and stabilizing coagulation factor VIII (FVIII) in circulation. Deficiency or dysfunction of VWF results in von Willebrand disease (VWD), the most common …

    queens Repository record for Understanding the Role of von Willebrand Factor (VWF) in Angiogenesis and Angiodysplasia (opens in a new tab)

  2. A genome-wide association study in chronic thromboembolic pulmonary hypertension and the ADAMTS13-VWF axis

    … variation in plasma von Willebrand factor (VWF) levels. Abnormalities in haemostasis are implicated in CTEPH pathobiology, including elevated levels of VWF, which is cleaved by ADAMTS13 (a disintegrin and metalloproteinase with a thrombospondin type 1 motif, member 13). The ADAMTS13-VWF axis …

    cambridge Repository record for A genome-wide association study in chronic thromboembolic pulmonary hypertension and the ADAMTS13-VWF axis (opens in a new tab)

  3. von Willebrand factor interaction with subendothelial collagens and platelet surface receptor GPIBalpha under shear conditions

    … platelet surface receptors GPIbalpha, multimeric vWf acts as a bridge between subendothelium and circulating platelets. In this study, the molecular binding between vWf multimers and human pepsin-digested collagen I, III and VI was characterized using Surface Plasmon Resonance (BIAcore). Compared …

    rice Repository record for von Willebrand factor interaction with subendothelial collagens and platelet surface receptor GPIBalpha under shear conditions (opens in a new tab)

  4. A Microfluidic Approach For Investigating The Role Of Blood Flow In Thrombosis

    … rates to aggregate von Willebrand factor (VWF) into insoluble fibers held in place by a micropost. VWF fibers were non-amyloid and resistant to ADAMTS13 and tissue plasminogen activator. Factors XIIa and XIa were captured in VWF fibers during aggregation, and could initiate fibrin formation …

    penn Repository record for A Microfluidic Approach For Investigating The Role Of Blood Flow In Thrombosis (opens in a new tab)

  5. Characterization of platelet glycoprotein Ib-IX-V: von Willebrand factor interaction under shear conditions

    … glycoprotein (GP) Ib and von Willebrand factor (VWF). In the first part of the work, we evaluated the kinetics of interaction between platelet GP Ib-IX-V complex and VWF under arterial flow conditions. The GP Ibalpha subunit of GP Ib complex binds to VWF through the Al domain of VWF. Impaired GP …

    rice Repository record for Characterization of platelet glycoprotein Ib-IX-V: von Willebrand factor interaction under shear conditions (opens in a new tab)

  6. Aberrant and Alternative Splicing of von Willebrand Factor

    … or qualitative defects of von Willebrand factor (VWF). VWD can be caused by a variety of mutations throughout the VWF gene, the majority of which are missense changes. Approximately 10% of pathologic VWF mutations are thought to disrupt the process of VWF splicing leading to VWD; however, this …

    queens Repository record for Aberrant and Alternative Splicing of von Willebrand Factor (opens in a new tab)

  7. The Role of YAP/TAZ in von Willebrand Factor Gene Expression

    von Willebrand Factor (VWF) is a large multimeric glycoprotein with important procoagulant roles in the circulation, including mediating platelet adhesion at sites of vascular injury and stabilizing Factor VIII in the plasma. VWF expression and activity is critically regulated to protect against …

    queens Repository record for The Role of YAP/TAZ in von Willebrand Factor Gene Expression (opens in a new tab)

  8. Interaction Between the Metalloprotease ADAMTS-13 and the Proteins of the Alternative Pathway of the Complement System

    Von Willebrand factor (VWF), a multimeric protein that has a central role in hemostasis, has been shown to interact with complement components. However results are contrasting and inconclusive. By studying 20 patients with congenital thrombotic thrombocytopenic purpura (cTTP) who can not cleave VWF

    the-open-u Repository record for Interaction Between the Metalloprotease ADAMTS-13 and the Proteins of the Alternative Pathway of the Complement System (opens in a new tab)

  9. Determination of ADAMTS13 Susceptibility in Type IIA von Willebrand Disease

    … caused by a deficiency in von Willebrand Factor (vWF), a large glycoprotein that assists in coagulation. Specifically, large vWF multimers in the blood stream are key components in starting the coagulation cascade. vWF is cleaved by the metalloprotease ADAMTS13, regulating the multimers size, …

    dominican Repository record for Determination of ADAMTS13 Susceptibility in Type IIA von Willebrand Disease (opens in a new tab)

  10. VON WILLEBRAND DISEASE: NEW INSIGHTS INTO THE EPIDEMIOLOGY, PATHOPHYSIOLOGY AND GENOTYPE/PHENOTYPE CORRELATION

    … della glicoproteina fattore di von Willebrand (VWF). Questa tesi mirava a fornire nuove informazioni sull'epidemiologia, la fisiopatologia e il genotipo/fenotipo della VWD. Abbiamo condotto 5 studi per affrontare questi obiettivi. (i) Analizzando i dati dell'esoma e del genoma di 141.456 …

    milano Repository record for VON WILLEBRAND DISEASE: NEW INSIGHTS INTO THE EPIDEMIOLOGY, PATHOPHYSIOLOGY AND GENOTYPE/PHENOTYPE CORRELATION (opens in a new tab)

  11. Effect of Levothyroxine Administration on Hemostatic Analytes in Doberman Pinschers with von Willebrand's Disease

    … increases plasma von Willebrand factor (vWf) concentration and enhances vWf function. The effects of levothyroxine administration were evaluated in 8 euthyroid Doberman Pinschers with plasma vWf concentration <30%. Levothyroxine (0.04mg/kg PO q12hours) and placebo were administered for 30 …

    vt Repository record for Effect of Levothyroxine Administration on Hemostatic Analytes in Doberman Pinschers with von Willebrand's Disease (opens in a new tab)

  12. PATHOPHYSIOLOGY OF VON WILLEBRAND FACTOR IN BLEEDING AND THROMBOSIS

    von Willebrand factor (VWF) is a multimeric glycoprotein mainly known to be involved in primary hemostasis recruiting platelets at the site of damaged vessels and acting as factor VIII (FVIII) carrier. Quantitative or qualitative alteration of VWF protein is responsible for von Willebrand disease …

    milano Repository record for PATHOPHYSIOLOGY OF VON WILLEBRAND FACTOR IN BLEEDING AND THROMBOSIS (opens in a new tab)

  13. Multi-scale computational modeling of particle adhesion dynamics under shear flow

    … description of the von Willebrand factor (VWF) mediated thrombus growth process was formulated. The physics-based model captures distinct stages of the thrombus growth process in shear-induced platelet adhesion (SIPA) and platelet-aggregate morphology. It describes platelets dynamics, VWF

    gatech Repository record for Multi-scale computational modeling of particle adhesion dynamics under shear flow (opens in a new tab)

  14. The role of von Willebrand factor and its cleaving protease, ADAMTS13, in young patients with HIV-related stroke.

    … adults. High levels of von Willebrand factor (VWF), a protein with key roles in platelet adhesion and aggregation, and low levels of A Disintegrin and Metalloproteinase with a Thrombospondin type 1 motif, member 13 (ADAMTS13), the protease that cleaves ultra large VWF multimers into smaller …

    cape-town Repository record for The role of von Willebrand factor and its cleaving protease, ADAMTS13, in young patients with HIV-related stroke. (opens in a new tab)

  15. CLINICAL AND LABORATORY CHARACTERISATION OF ACQUIRED VON WILLEBRAND SYNDROME

    … disorder due to reduced or dysfunctional VWF in individuals without a personal or familial bleeding history. It is associated with systemic diseases such as lymphoproliferative (LPDs) and myeloproliferative neoplasms (MPNs), cardiovascular, and autoimmune conditions. The underlying …

    milano Repository record for CLINICAL AND LABORATORY CHARACTERISATION OF ACQUIRED VON WILLEBRAND SYNDROME (opens in a new tab)

  16. Role of von Willebrand factor in shear induced platelet accumulation in a microfluidic device

    … via the glycoprotein von Willebrand factor (vWF). To investigate the relative contributions of vWF and platelets in high shear thrombosis, the present work developed a microfluidic thrombosis assay to meet low blood volume requirements and fluid shear conditions (3500-6000 s-1). Microfluidic …

    gatech Repository record for Role of von Willebrand factor in shear induced platelet accumulation in a microfluidic device (opens in a new tab)

  17. Vibration-induced white finger in dockyard employees

    Vibration-induced white finger (VWF) is a vascular condition associated with occupational exposure to hand-transmitted vibration. The fingers are prone to intermittent blanching attacks which may be triggered by cold conditions and are usually accompanied by numbness and tingling or pain. VWF has …

    soton Repository record for Vibration-induced white finger in dockyard employees (opens in a new tab)

  18. Genetic characterization of families with von Willebrand disease

    … defects of the von Willebrand factor (VWF). The severity of the disease can vary considerably, as can the hereditary patterns. The variable phenotypes of VWD have given rise to a classification scheme that divides the disease into three types according to how it is manifested and …

    lund Repository record for Genetic characterization of families with von Willebrand disease (opens in a new tab)

  19. Die Wirkung von niedrig dosiertem Desmopressin auf die durch Acetylsalicylsäure verlängerte Blutungszeit

    … von FVIII und den von Willebrand-Faktor (vWF) ist lange bekannt und gut untersucht. Zur Erklärung dieser Beobachtung wird meist die plättchenadhäsive Wirkung des vWF genannt. Obwohl die Bedeutung der vor¬liegenden Daten zur vWF-/FVIII-Freisetzung für die Therapie von Plättchenstörungen …

    goettingen Repository record for Die Wirkung von niedrig dosiertem Desmopressin auf die durch Acetylsalicylsäure verlängerte Blutungszeit (opens in a new tab)

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