Functional characterization of human blood coagulation factor XIa using hybridoma antibodies.
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference29 articles.
1. New Hemophilia-like Disease Caused by Deficiency of a Third Plasma Thromboplastin Factor.
2. Isolation and characterization of bovine factor XI (plasma thromboplastin antecedent)
3. Activation of human factor XI (plasma thromboplastin antecedent) by factor XIIa (activated Hageman factor)
4. Human blood coagulation factor XI. Purification, properties, and mechanism of activation by activated factor XII.
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1. Coagulation Factor XIa;Handbook of Proteolytic Enzymes;2013
2. Productive Recognition of Factor IX by Factor XIa Exosites Requires Disulfide Linkage between Heavy and Light Chains of Factor XIa;Journal of Biological Chemistry;2012-02
3. The Role of Factor XIa (FXIa) Catalytic Domain Exosite Residues in Substrate Catalysis and Inhibition by the Kunitz Protease Inhibitor Domain of Protease Nexin 2;Journal of Biological Chemistry;2011-09
4. Solution structure of the A4 domain of factor XI sheds light on the mechanism of zymogen activation;Proceedings of the National Academy of Sciences;2007-09-20
5. Macromolecular Substrate-Binding Exosites on Both the Heavy and Light Chains of Factor XIa Mediate the Formation of the Michaelis Complex Required for Factor IX-Activation;Biochemistry;2007-08-01
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