Expression studies on a novel type 2B variant of the von Willebrand factor gene (R1308L) characterized by defective collagen binding
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1538-7836.2005.01638.x/fullpdf
Reference17 articles.
1. A Revised Classification of von Willebrand Disease
2. Initiation of Platelet Adhesion by Arrest onto Fibrinogen or Translocation on von Willebrand Factor
3. Heightened Interaction between Platelets and Factor VIII/von Willebrand Factor in a New Subtype of von Willebrand's Disease
4. Platelet Aggregation Induced by I-Desamino-8-D-Arginine Vasopressin (dDAVP) in Type IIb von Willebrand's Disease
5. A new von Willebrand variant (type I, New York): increased ristocetin- induced platelet aggregation and plasma von Willebrand factor containing the full range of multimers
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1. The dominant p.Thr274Pro mutation in the von Willebrand factor propeptide causes the von Willebrand disease type 1 phenotype in two unrelated patients;Haemophilia;2022-01-22
2. Shear Stress Accumulation Enhances von Willebrand Factor-Induced Platelet P-Selectin Translocation in a PI3K/Akt Pathway-Dependent Manner;Frontiers in Cell and Developmental Biology;2021-06-01
3. Genetic Background of von Willebrand Disease: History, Current State, and Future Perspectives;Seminars in Thrombosis and Hemostasis;2019-12-30
4. The Von Willebrand Factor A1–Collagen III Interaction Is Independent of Conformation and Type 2 Von Willebrand Disease Phenotype;Journal of Molecular Biology;2017-01
5. Phenotypic Parameters in Genotypically Selected Type 2B von Willebrand Disease Patients: A Large, Single-Center Experience Including a New Novel Mutation;Seminars in Thrombosis and Hemostasis;2016-12-15
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