Suchergebnis | Hamburg Open Science

Facetten

16 Einträge gefunden

Upshaw-Schulman syndrome-associated ADAMTS13 variants possess proteolytic activity at the surface of endothelial cells and in simulated circulation
2020 - Forschungsinformationssystem des UKE
Alteration in GPIIb/IIIa Binding of VWD-Associated von Willebrand Factor Variants with C-Terminal Missense Mutations
2019 - Forschungsinformationssystem des UKE
Advancing multimer analysis of von Willebrand factor by single-molecule AFM imaging
2019 - Forschungsinformationssystem des UKE - frei zugänglich
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
von Willebrand factor is dimerized by protein disulfide isomerase
2016 - Forschungsinformationssystem des UKE
Von Willebrand factor regulates complement on endothelial cells
2016 - Forschungsinformationssystem des UKE
Distinct mechanisms account for acquired von Willebrand syndrome in plasma cell dyscrasias
2016 - 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
Inherited thrombotic thrombocytopenic purpura in children
2014 - Forschungsinformationssystem des UKE
Correction of acquired von Willebrand syndrome by transcatheter aortic valve implantation
2014 - Forschungsinformationssystem des UKE
The mutation N528S in the von Willebrand factor (VWF) propeptide causes defective multimerization and storage of VWF.
2010 - Forschungsinformationssystem des UKE
A cluster of mutations in the D3 domain of von Willebrand factor correlates with a distinct subgroup of von Willebrand disease: type 2A/IIE.
2010 - Forschungsinformationssystem des UKE
Impact of mutations in the von Willebrand factor A2 domain on ADAMTS13-dependent proteolysis.
2006 - Forschungsinformationssystem des UKE
The spectrum of aldolase B (ALDOB) mutations and the prevalence of hereditary fructose intolerance in Central Europe.
2005 - Forschungsinformationssystem des UKE
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

Aktive Facetten

Facetten

Zugriff

Einrichtung

Medientyp

Karte

Erscheinungsjahr

Autor/in

Sprache

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

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

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

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

von Willebrand factor is dimerized by protein disulfide isomerase

Von Willebrand factor regulates complement on endothelial cells

Distinct mechanisms account for acquired von Willebrand syndrome in plasma cell dyscrasias

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

Inherited thrombotic thrombocytopenic purpura in children

Correction of acquired von Willebrand syndrome by transcatheter aortic valve implantation

The mutation N528S in the von Willebrand factor (VWF) propeptide causes defective multimerization and storage of VWF.

A cluster of mutations in the D3 domain of von Willebrand factor correlates with a distinct subgroup of von Willebrand disease: type 2A/IIE.

Impact of mutations in the von Willebrand factor A2 domain on ADAMTS13-dependent proteolysis.

The spectrum of aldolase B (ALDOB) mutations and the prevalence of hereditary fructose intolerance in Central Europe.

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