Specificity of inhibitors lacking in alpha1 antitrypsin deficiency and hereditary angioedema toward human proteolytic enzymes
- 1 June 1972
- journal article
- Published by Elsevier in Clinica Chimica Acta; International Journal of Clinical Chemistry
- Vol. 39 (1) , 5-14
- https://doi.org/10.1016/0009-8981(72)90293-8
Abstract
No abstract availableKeywords
This publication has 24 references indexed in Scilit:
- Activation of plasminogen by human plasma kallikreinPublished by Elsevier ,2004
- Genetically determined heterogeneity of the C1 esterase inhibitor in patients with hereditary angioneurotic edemaJournal of Clinical Investigation, 1971
- HUMAN PLASMA ALPHA 2-MACROGLOBULINThe Journal of Experimental Medicine, 1970
- Permeability-increasing activity in hereditary angioneurotic edema plasmaJournal of Clinical Investigation, 1969
- Effect of proteolytic enzymes on bovine factor V. I. Kinetics of activation and inactivation by bovine thrombinBiochemistry, 1969
- Studies on the prekallikrein (kallikreinogen)-kallikrein enzyme system of human plasmaJournal of Clinical Investigation, 1969
- The plasmin inhibitors of human plasmaBiochimica et Biophysica Acta (BBA) - General Subjects, 1966
- Hereditary Angioneurotic Edema: Two Genetic VariantsScience, 1965
- Action of Complement in Hereditary Angioneurotic Edema: The Role of C′1-Esterase *Journal of Clinical Investigation, 1964
- Hereditary angioneurotic edema: II. Deficiency of inhibitor for serum globulin permeability factor and/or plasma kallikreinJournal of Allergy, 1962