Julia Driesen

Bonn, NW, Germany

Last Updated: 09/26/2026

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Found 10 publications

An in silico and in vitro approach to elucidate the impact of residues flanking the cleavage scissile bonds of FVIII.

An in silico and in vitro approach to elucidate the impact of residues flanking the cleavage scissile bonds of FVIII.

Journal: PloS one
Published: January 16, 2017

Transcatheter aortic valve implantation leads to a restoration of von Willebrand factor (VWF) abnormalities in patients with severe aortic stenosis - Incidence and relevance of clinical and subclinical VWF dysfunction in patients undergoing transfemoral TAVI.

Transcatheter aortic valve implantation leads to a restoration of von Willebrand factor (VWF) abnormalities in patients with severe aortic stenosis - Incidence and relevance of clinical and subclinical VWF dysfunction in patients undergoing transfemoral TAVI.

Journal: Thrombosis research
Published: July 22, 2016

Intron retention resulting from a silent mutation in the VWF gene that structurally influences the 5' splice site.

Intron retention resulting from a silent mutation in the VWF gene that structurally influences the 5' splice site.

Journal: Blood
Published: February 12, 2016

Congenital combined deficiency of coagulation factors VII and X--different genetic mechanisms.

Congenital combined deficiency of coagulation factors VII and X--different genetic mechanisms.

Journal: Haemophilia : the official journal of the World Federation of Hemophilia
Published: November 13, 2014

Insights into pathological mechanisms of missense mutations in C-terminal domains of von Willebrand factor causing qualitative or quantitative von Willebrand disease.

Insights into pathological mechanisms of missense mutations in C-terminal domains of von Willebrand factor causing qualitative or quantitative von Willebrand disease.

Journal: Haematologica
Published: March 30, 2013

ATZ11 recognizes not only Z-α1-antitrypsin-polymers and complexed forms of non-Z-α1-antitrypsin but also the von Willebrand factor.

ATZ11 recognizes not only Z-α1-antitrypsin-polymers and complexed forms of non-Z-α1-antitrypsin but also the von Willebrand factor.

Journal: PloS one
Published: March 28, 2013

Effect of F8 B domain gene variants on synthesis, secretion, activity and stability of factor VIII protein.

Effect of F8 B domain gene variants on synthesis, secretion, activity and stability of factor VIII protein.

Journal: Thrombosis and haemostasis
Published: January 14, 2013

In vitro characterization of recombinant factor VIII concentrates reveals significant differences in protein content, activity and thrombin activation profile.

In vitro characterization of recombinant factor VIII concentrates reveals significant differences in protein content, activity and thrombin activation profile.

Journal: Haemophilia : the official journal of the World Federation of Hemophilia
Published: November 12, 2012

Mutation distribution in the von Willebrand factor gene related to the different von Willebrand disease (VWD) types in a cohort of VWD patients.

Mutation distribution in the von Willebrand factor gene related to the different von Willebrand disease (VWD) types in a cohort of VWD patients.

Journal: Thrombosis and haemostasis
Published: February 16, 2012

Deficiencies of antithrombin, protein C and protein S - practical experience in genetic analysis of a large patient cohort.

Deficiencies of antithrombin, protein C and protein S - practical experience in genetic analysis of a large patient cohort.

Journal: Thrombosis and haemostasis
Published: December 20, 2011
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Last Updated: 09/26/2026