Abnormal von Willebrand factor in bleeding angiodysplasias of the digestive tract |
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Acquired von Willebrand syndrome: data from an international registry. |
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Analysis of von Willebrand factor mRNA from the lung of pigs with severe von Willebrand disease by using a human cDNA probe |
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Aplastic anemia presenting as spontaneous orbital hemorrhage |
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APPORT DES DIFFERENTES METHODES DE DOSAGE DES PRODUITS DE DEGRADATION DU FIBRINOGENE ET DE LA FIBRINE AU DIAGNOSTIC ET AU SUIVI EVOLUTIF DES COAGULATIONS INTRAVASCULAIRES DISSEMINEES |
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Assessment of the expression of candidate human plasma membrane phospholipid scramblase in Scott syndrome cells |
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CARACTERISATION DE LA REGION 5' DU GENE DU FACTEUR WILLEBRAND BOVIN COMPARAISON DE L'ACTIVITE FONCTIONNELLE DES PROMOTEURS DU GENE HUMAIN ET BOVIN DANS LES CELLULES ENDOTHELIALES |
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Carbon monoxide exposure in the urban environment: an insidious foe for the heart? |
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Carbon monoxide pollution impairs myocardial perfusion reserve: implication of coronary endothelial dysfunction. |
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Characterization of recombinant von Willebrand factors mutated on cysteine 509 or 695. |
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Comparison of FRETS-VWF73 to full-length VWF as a substrate for ADAMTS13 activity measurement in human plasma samples |
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Cyclic adenosine monophosphate-dependent mechanisms induce von Willebrand factor expression in the Dami megakaryoblastic cell line. |
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Effet des variations in vivo de la concentration plasmatique de lipoproteine(a) sur la formation de plasmine |
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Estimation of the von Willebrand factor-cleaving protease in plasma using monoclonal antibodies to vWF. |
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Etude fonctionnelle des interactions entre le facteur willebrand et ses récepteurs : Vaisseaux-hémostase-coagulation |
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ETUDE IN VITRO DE LA LIAISON DU FACTEUR WILLEBRAND A L'HEPARINE ET A SES DERIVES |
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Evidence that a secondary binding and protecting site for factor VIII on von Willebrand factor is highly unlikely |
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Exercise-induced cardioprotection: a role for eNOS uncoupling and NO metabolites. |
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Factor VIII and IX variants. Relationship between haemophilia B M and haemophilia B+. |
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Generation of von Willebrand factor epitope libraries expressed in E. coli |
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Heterogeneity of von Willebrand's disease: study of 40 Iranian cases |
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Hydrogénations asymétriques de deshydropeptides catalysées par des complexes chiraux du rhodium |
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Identification of a CpG mutation in the coagulation factor-IX gene by analysis of amplified DNA sequences |
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Immort'elles : Florence Delay, Brigitte Terziev, Dominique Meyer, Edith Canat de Chizy |
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Immort'elles. Oeuvres gravées. Anne-Catherine Nesa |
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Impaired megakaryocytopoiesis in type 2B von Willebrand disease with severe thrombocytopenia |
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Influence of high ionic strength buffers on factor VIII/von Willebrand factor from different species |
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Influence of mutations and size of multimers in type II von Willebrand disease upon the function of von Willebrand factor. |
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Interactions de la protéase spécifique et d'anticorps developpés chez des patients atteints de maladie de Willebrand sévère avec le facteur Willebrand |
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Moderate exercise prevents impaired Ca2+ handling in heart of CO-exposed rat: implication for sensitivity to ischemia-reperfusion |
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Modification des fonctions plaquettaires induites par les contraintes de cisaillement hémodynamiques |
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Modification ofplatelet functions induced by shear. |
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Molecular genetics of type 2 von Willebrand disease |
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A monoclonal antibody (B724) to von Willebrand factor recognizing an epitope within the A1 disulphide loop (Cys509-Cys695) discriminates between type 2A and type 2B von Willebrand disease |
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Mutations C1157F and C1234W of von Willebrand factor cause intracellular retention with defective multimerization and secretion |
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NOUVELLES METHODES D'EXPLORATION BIOLOGIQUE DE LA MALADIE DE WILLEBRAND (DES BIOL. MED.) |
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A novel case of compound heterozygosity with "Normandy"/type I von Willebrand disease (vWD). Direct demonstration of the segregation of one allele with a defective expression at the mRNA level causing type I vWD. |
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Optimization of the transfection of human endothelial cells by electroporation |
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Patho-physiological interaction of von willebrand factor with platelets : binding to glycoprotein IIb/IIIa and influence of shear stress of microcirculation. |
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Platelet membrane glycoproteins implicated in ristocetin-induced aggregation. Studies of the proteins on platelets from patients with Bernard-Soulier syndrome and von Willebrand's disease |
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Primary structure of the factor VIII binding domain of human, porcine and rabbit von Willebrand factor. |
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Prognostic value of anti-ADAMTS 13 antibody features (Ig isotype, titer, and inhibitory effect) in a cohort of 35 adult French patients undergoing a first episode of thrombotic microangiopathy with undetectable ADAMTS 13 activity |
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THE PROMOTOR REGION FOR THE VON WILLEBRAND FACTOR GENE : CHARACTERIZATION AND FUNCTIONAL ANALYSIS. |
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Relation structure-functions of the couple Von Willebrand factor-ADAMTS13. |
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Requirement of prestimulated THP-1 monocytic cells for endothelial cell activation. Involvement of TNF alpha |
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The role of the 5'-flanking region in the cell-specific transcription of the human von Willebrand factor gene |
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Scott syndrome: an inherited defect of the procoagulant activity of platelets |
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Séance publique annuelle des cinq académies, mardi 26 octobre 2004 |
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Ser968Thr mutation within the A3 domain of von Willebrand factor (VWF) in two related patients leads to a defective binding of VWF to collagen. |
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A simple and efficient method for isolating high molecular weight DNA from mammalian sperm |
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Simulated urban carbon monoxide air pollution exacerbates rat heart ischemia-reperfusion injury |
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Ten candidate ADAMTS13 mutations in six French families with congenital thrombotic thrombocytopenic purpura (Upshaw-Schulman syndrome). |
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LES THROMBOPENIES INDUITES PAR L'HEPARINE IDENTIFICATION DES CIBLES ANTIGENIQUES, MECANISMES D'ACTION ET APPLICATIONS CLINIQUES |
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Thrombotic thrombocytopenic purpura associated with von Willebrand factor-cleaving protease (ADAMTS13) deficiency in children |
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Thrombotic thrombocytopenic purpura with severe ADAMTS-13 deficiency in two patients with primary antiphospholipid syndrome |
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Trafic intracellulaire dans la lignée mégacaryocyto-plaquettaire : biogenèse des granules denses et interaction avec le virus de l'immunodéficience humaine |
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Update on the pathophysiology and classification of von Willebrand disease: a report of the Subcommittee on von Willebrand Factor |
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Vitronectin receptor biosynthesis and maturation in endothelial cells. |
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