Literature DB >> 11057844

Deficiency causing mutations and common polymorphisms in the factor XIII-A gene.

L Muszbek1.   

Abstract

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Year:  2000        PMID： 11057844

Source DB:  PubMed          Journal:  Thromb Haemost        ISSN： 0340-6245            Impact factor:   5.249


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  6 in total

1.  Impact of FXIII-A Val34Leu polymorphism on coronary artery disease in Croatian patients.

Authors:  Ana Bronić; Goran Ferencak; Renata Zadro; Ana Stavljenić-Rukavina; Robert Bernat
Journal:  Mol Biol Rep       Date:  2007-09-27       Impact factor: 2.316

Review 2.  Newly-Recognized Roles of Factor XIII in Thrombosis.

Authors:  James R Byrnes; Alisa S Wolberg
Journal:  Semin Thromb Hemost       Date:  2016-04-07       Impact factor: 4.180

3.  The factor XIII-A Val34Leu polymorphism decreases whole blood clot mass at high fibrinogen concentrations.

Authors:  Sravya Kattula; Zsuzsa Bagoly; Noémi Klára Tóth; László Muszbek; Alisa S Wolberg
Journal:  J Thromb Haemost       Date:  2020-02-28       Impact factor: 5.824

Review 4.  Role, Laboratory Assessment and Clinical Relevance of Fibrin, Factor XIII and Endogenous Fibrinolysis in Arterial and Venous Thrombosis.

Authors:  Vassilios P Memtsas; Deepa R J Arachchillage; Diana A Gorog
Journal:  Int J Mol Sci       Date:  2021-02-02       Impact factor: 5.923

Review 5.  Factor XIII and Fibrin Clot Properties in Acute Venous Thromboembolism.

Authors:  Michał Ząbczyk; Joanna Natorska; Anetta Undas
Journal:  Int J Mol Sci       Date:  2021-02-05       Impact factor: 5.923

Review 6.  Catridecacog: a breakthrough in the treatment of congenital factor XIII A-subunit deficiency?

Authors:  Wolfgang Korte
Journal:  J Blood Med       Date:  2014-07-09
  6 in total

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