H. Yadegari

发表

von Willebrand factor propeptide missense variants affect anterograde transport to Golgi resulting in ER retention

A. Biswas, J. Oldenburg, A. Naz, 2021, Human mutation.

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

A. Biswas, J. Oldenburg, A. Pavlova, 2013, Haematologica.

Von Willebrand factor propeptide and pathophysiological mechanisms in European and Iranian patients with type 3 von Willebrand disease enrolled in the 3WINTERS‐IPS study

F. Rosendaal, P. Mannucci, A. Tosetto, 2022, Journal of thrombosis and haemostasis : JTH.

The Current Understanding of Molecular Pathogenesis of Quantitative von Willebrand Disease, Types 1 and 3

J. Oldenburg, H. Yadegari, 2020, Hämostaseologie.

Exploring the structural similarity yet functional distinction between coagulation factor XIII-B and complement factor H sushi domains

A. Biswas, J. Oldenburg, Sneha Singh, 2019, Journal of Thrombosis and Thrombolysis.

ATZ11 Recognizes Not Only Z-α1-Antitrypsin-Polymers and Complexed Forms of Non-Z-α1-Antitrypsin but Also the von Willebrand Factor

D. Goltz, S. Steiner, J. Driesen, 2014, PloS one.

Large deletions identified in patients with von Willebrand disease using multiple ligation‐dependent probe amplification

J. Oldenburg, A. Pavlova, J. Driesen, 2011, Journal of thrombosis and haemostasis : JTH.

Disruption of Structural Disulfides of Coagulation FXIII-B Subunit; Functional Implications for a Rare Bleeding Disorder

A. Biswas, J. Oldenburg, Sneha Singh, 2019, International journal of molecular sciences.

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

A. Biswas, J. Oldenburg, A. Pavlova, 2012, Thrombosis and Haemostasis.

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

A. Biswas, J. Oldenburg, J. Driesen, 2016, Blood.

A Homozygous Deep Intronic Variant Causes Von Willebrand Factor Deficiency and Lack of Endothelial-Specific Secretory Organelles, Weibel–Palade Bodies

M. Jamil, J. Oldenburg, H. Yadegari, 2022, International journal of molecular sciences.

Ex Vivo Modeling of the PC (Protein C) Pathway Using Endothelial Cells and Plasma: A Personalized Approach

H. Yadegari, J. Oldenburg, N. S. Hamedani, 2022, Arteriosclerosis, thrombosis, and vascular biology.

Multifaceted pathomolecular mechanism of a VWF large deletion involved in the pathogenesis of severe VWD

M. Jamil, J. Oldenburg, O. el-Maarri, 2021, Blood advances.

Characterization of the mutation spectrum in a Pakistani cohort of type 3 von Willebrand disease

A. Biswas, J. Oldenburg, A. Pavlova, 2019, Haemophilia : the official journal of the World Federation of Hemophilia.

Potentials of Endothelial Colony-Forming Cells: Applications in Hemostasis and Thrombosis Disorders, from Unveiling Disease Pathophysiology to Cell Therapy

H. Yadegari, N. Schwarz, 2023, Hämostaseologie.