Major carboxypeptidase N deficiency
Author:
Publisher
Elsevier BV
Subject
Biochemistry, medical,Clinical Biochemistry,Biochemistry,General Medicine
Reference8 articles.
1. Carboxypeptidase N: a pleiotropic regulator of inflammation;Mathews;Mol Immunol,2004
2. Familial carboxypeptidase N deficiency;Mathews;Ann Int Med,1980
3. Assay of carboxypeptidase N activity in serum by liquid chromatographic detection of hippuric acid;Hendriks;Clin Chem,1985
4. A rapid and sensitive assay for the quantitation of carboxypeptidase N;Willemse;Clin Chim Acta,2006
5. Limited mutagenesis increases the stability of human carboxypeptidase U (TAFIa) and demonstrates the importance of CPU stability over proCPU concentration in down-regulating fibrinolysis;Knecht;Febs J,2006
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1. Hereditary angioedema with normal C1 inhibitor associated with carboxypeptidase N deficiency;Journal of Allergy and Clinical Immunology: Global;2024-05
2. Carboxypeptidase B2 and carboxypeptidase N in the crosstalk between coagulation, thrombosis, inflammation, and innate immunity;Journal of Thrombosis and Haemostasis;2018-07-11
3. Genetics of Hereditary Angioedema Revisited;Clinical Reviews in Allergy & Immunology;2016-04-26
4. Lysine Carboxypeptidase/Carboxypeptidase N;Handbook of Proteolytic Enzymes;2013
5. Binding of carboxypeptidase N to fibrinogen and fibrin;Biochemical and Biophysical Research Communications;2012-10
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