Literature DB >> 22004444

A family with type 2M VWD with normal VWF:RCo but reduced VWF:CB and a M1761K mutation in the A3 domain.

D Keeling, J Beavis, R Marr, K Sukhu, P Bignell.   

Abstract

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Year:  2011        PMID： 22004444     DOI： 10.1111/j.1365-2516.2011.02676.x

Source DB:  PubMed          Journal:  Haemophilia        ISSN： 1351-8216            Impact factor:   4.287


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  5 in total

1.  Crucial role for the VWF A1 domain in binding to type IV collagen.

Authors:  Veronica H Flood; Abraham C Schlauderaff; Sandra L Haberichter; Tricia L Slobodianuk; Paula M Jacobi; Daniel B Bellissimo; Pamela A Christopherson; Kenneth D Friedman; Joan Cox Gill; Raymond G Hoffmann; Robert R Montgomery
Journal:  Blood       Date:  2015-02-06       Impact factor: 22.113

2.  Defective collagen binding and increased bleeding in a murine model of von Willebrand disease affecting collagen IV binding.

Authors:  T L Slobodianuk; C Kochelek; J Foeckler; S Kalloway; H Weiler; V H Flood
Journal:  J Thromb Haemost       Date:  2018-12-18       Impact factor: 5.824

3.  Identification of a missense mutation (p.Leu1733Pro) in the A3 domain of von Willebrand factor in a family with type 2M von Willebrand disease.

Authors:  Toshio Shigekiyo; Hikaru Yagi; Etsuko Sekimoto; Hironobu Shibata; Shuji Ozaki; Masanori Matsumoto
Journal:  Int J Hematol       Date:  2019-10-11       Impact factor: 2.490

Review 4.  New insights into genotype and phenotype of VWD.

Authors:  Veronica H Flood
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2014-11-18

Review 5.  Current issues in diagnosis and treatment of von Willebrand disease.

Authors:  Daniel A Keesler; Veronica H Flood
Journal:  Res Pract Thromb Haemost       Date:  2017-12-12
  5 in total

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