A familial factor XIII subunit B deficiency
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.1990.00282.x-i1/fullpdf
Reference20 articles.
1. Performance characteristics of a commercial kit for assay of factor VIII-related antigen;Cejka;Clinical Chemistry,1984
2. Gerinnungsphysiologische Schnellmethode zur Bestimmung des Fibrinogens;Clauss;Acta Haematologica (Basel),1957
3. Calcium-induced dissociation of human plasma factor XIII and the appearance of catalytic activity;Cooke;Biochemical Journal,1974
4. A hitherto undescribed congenital haemorrhagic diathesis probably due to fibrin stabilizing factor deficiency;Duckert;Thrombosis et Diathesis Haemorrhagica,1960
5. The (μ-glutamyl) lysine crosslink and catalytic role of transglutaminase;Folk;Advances in Protein Chemistry,1977
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1. Reciprocal stabilization of coagulation factor XIII-A and -B subunits is a determinant of plasma FXIII concentration;Blood;2024-02-01
2. The History of Factor XIII Deficiency;Seminars in Thrombosis and Hemostasis;2023-01-27
3. An international collaborative study to assign value for Total Factor XIII‐B Subunit Antigen to the WHO 1st International Standard for Factor XIII Plasma, (02/206): Communication from the ISTH SSC Subcommittee on Factor XIII and Fibrinogen;Journal of Thrombosis and Haemostasis;2021-11-30
4. N‐glycosylation of blood coagulation factor XIII subunit B and its functional consequence;Journal of Thrombosis and Haemostasis;2020-04-15
5. Auto‐ and alloantibodies against factorXIII: laboratory diagnosis and clinical consequences;Journal of Thrombosis and Haemostasis;2018-03-23
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