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20 Einträge gefunden

Genotypes of European and Iranian patients with type 3 von Willebrand disease enrolled in 3WINTERS-IPS
2021 - Forschungsinformationssystem des UKE - frei zugänglich
Comparison of von Willebrand factor platelet-binding activity assays:ELISA overreads type 2B with loss of HMW multimers
2020 - Forschungsinformationssystem des UKE
Upshaw-Schulman syndrome-associated ADAMTS13 variants possess proteolytic activity at the surface of endothelial cells and in simulated circulation
2020 - Forschungsinformationssystem des UKE
Advancing multimer analysis of von Willebrand factor by single-molecule AFM imaging
2019 - Forschungsinformationssystem des UKE - frei zugänglich
Alteration in GPIIb/IIIa Binding of VWD-Associated von Willebrand Factor Variants with C-Terminal Missense Mutations
2019 - Forschungsinformationssystem des UKE
Characterization of VWF gene conversions causing von Willebrand disease
2019 - Forschungsinformationssystem des UKE
Genetic and Functional Characterization of ADAMTS13 Variants in a Patient Cohort with Upshaw-Schulman Syndrome Investigated in Germany
2018 - Forschungsinformationssystem des UKE
Mutation G1629E Increases von Willebrand Factor Cleavage via a Cooperative Destabilization Mechanism
2017 - Forschungsinformationssystem des UKE
Von Willebrand factor regulates complement on endothelial cells
2016 - Forschungsinformationssystem des UKE
Shear-Induced Unfolding and Enzymatic Cleavage of Full-Length VWF Multimers
2016 - Forschungsinformationssystem des UKE
Update on von Willebrand factor multimers: focus on high-molecular-weight multimers and their role in hemostasis
2014 - Forschungsinformationssystem des UKE
Inherited thrombotic thrombocytopenic purpura in children
2014 - Forschungsinformationssystem des UKE
Characterisation of the p.A1461D mutation causing von Willebrand disease type 2B with severe thrombocytopenia, circulating giant platelets, and defective α-granule secretion
2014 - Forschungsinformationssystem des UKE
Performance evaluation and multicentre study of a von Willebrand factor activity assay based on GPIb binding in the absence of ristocetin
2014 - Forschungsinformationssystem des UKE
Acquired hemophilia A and von Willebrand syndrome in a patient with late-onset systemic lupus erythematosus
2014 - Forschungsinformationssystem des UKE - frei zugänglich
Phenotypic and molecular characterisation of type 3 von Willebrand disease in a cohort of Indian patients
2013 - Forschungsinformationssystem des UKE
Characterisation of mutations and molecular studies of type 2 von Willebrand disease.
2013 - Forschungsinformationssystem des UKE
Exponential size distribution of von Willebrand factor
2013 - Forschungsinformationssystem des UKE
Inflammation-associated ADAMTS13 deficiency promotes formation of ultra-large von Willebrand factor.
2008 - Forschungsinformationssystem des UKE - frei zugänglich
Recombinant expression of mutations causing von Willebrand disease type Normandy: characterization of a combined defect of factor VIII binding and multimerization.
2004 - Forschungsinformationssystem des UKE

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Genotypes of European and Iranian patients with type 3 von Willebrand disease enrolled in 3WINTERS-IPS

Comparison of von Willebrand factor platelet-binding activity assays:ELISA overreads type 2B with loss of HMW multimers

Upshaw-Schulman syndrome-associated ADAMTS13 variants possess proteolytic activity at the surface of endothelial cells and in simulated circulation

Advancing multimer analysis of von Willebrand factor by single-molecule AFM imaging

Alteration in GPIIb/IIIa Binding of VWD-Associated von Willebrand Factor Variants with C-Terminal Missense Mutations

Characterization of VWF gene conversions causing von Willebrand disease

Genetic and Functional Characterization of ADAMTS13 Variants in a Patient Cohort with Upshaw-Schulman Syndrome Investigated in Germany

Mutation G1629E Increases von Willebrand Factor Cleavage via a Cooperative Destabilization Mechanism

Von Willebrand factor regulates complement on endothelial cells

Shear-Induced Unfolding and Enzymatic Cleavage of Full-Length VWF Multimers

Update on von Willebrand factor multimers: focus on high-molecular-weight multimers and their role in hemostasis

Inherited thrombotic thrombocytopenic purpura in children

Characterisation of the p.A1461D mutation causing von Willebrand disease type 2B with severe thrombocytopenia, circulating giant platelets, and defective α-granule secretion

Performance evaluation and multicentre study of a von Willebrand factor activity assay based on GPIb binding in the absence of ristocetin

Acquired hemophilia A and von Willebrand syndrome in a patient with late-onset systemic lupus erythematosus

Phenotypic and molecular characterisation of type 3 von Willebrand disease in a cohort of Indian patients

Characterisation of mutations and molecular studies of type 2 von Willebrand disease.

Exponential size distribution of von Willebrand factor

Inflammation-associated ADAMTS13 deficiency promotes formation of ultra-large von Willebrand factor.

Recombinant expression of mutations causing von Willebrand disease type Normandy: characterization of a combined defect of factor VIII binding and multimerization.