Mutations in the D′D3 region of VWF traditionally associated with type 1 VWD lead to quantitative and qualitative deficiencies of VWF-Reference-Cited by-同舟云学术

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Mutations in the D′D3 region of VWF traditionally associated with type 1 VWD lead to quantitative and qualitative deficiencies of VWF

Published:2016-09 Issue: Volume:145 Page:112-118
ISSN:0049-3848
Container-title:Thrombosis Research
language:en
Short-container-title:Thrombosis Research

Author:

White-Adams Tara C.,Ng Christopher J.,Jacobi Paula M.,Haberichter Sandra L.,Di Paola Jorge A.

Funder

Postle Chair in Pediatric Blood Disorders

Judith Graham Pool Award of the National Hemophilia Foundation

Publisher

Elsevier BV

Subject

Hematology

Reference25 articles.

1. Synthesis of antihemophilic factor antigen by cultured human endothelial cells;Jaffe;J. Clin. Invest.,1973

2. Synthesis of factor VIII antigen by cultured guinea pig megakaryocytes;Nachman;J. Clin. Invest.,1977

3. Full-length von Willebrand factor (vWF) cDNA encodes a highly repetitive protein considerably larger than the mature vWF subunit;Verweij;EMBO J.,1986

4. Von Willebrand factor, Jedi knight of the bloodstream;Springer;Blood,2014

5. Basal secretion of von Willebrand factor from human endothelial cells;Giblin;Blood,2008

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2. Phenotypic and genetic characterizations of the Milan cohort of von Willebrand disease type 2;Blood Advances;2022-07-11

3. Single-cell transcriptional analysis of human endothelial colony-forming cells from patients with low VWF levels;Blood;2022-04-07

4. Genotypes of European and Iranian patients with type 3 von Willebrand disease enrolled in 3WINTERS-IPS;Blood Advances;2021-08-05

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