A model to explain the pharmacological effects of snake venom phospholipases A2
- 1 January 1989
- Vol. 27 (6) , 613-635
- https://doi.org/10.1016/0041-0101(89)90013-5
Abstract
No abstract availableKeywords
This publication has 122 references indexed in Scilit:
- Toxicity domain in presynaptically toxic phospholipase A2 of snake venomBiochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology, 1987
- Specific binding of three neurotoxins with phospholipase A2 activity to synaptosomal membrane preparations from the guinea pig brainProtein Journal, 1986
- Selective modification of tyrosine-68 in β1-bungarotoxin from the venom ofBungarus multicinctus (Taiwan banded krait)Protein Journal, 1986
- Cardiotoxic effects of venom phospholipase A2 are not due to phospholipid hydrolytic productsLife Sciences, 1984
- Potent platelet aggregation inhibitor from Trimeresurus gramineus snake venomBiochimica et Biophysica Acta (BBA) - General Subjects, 1983
- Effect of methylation of histidine-48 on some enzymatic and pharmacological activities of snake venom phospholipases A2Life Sciences, 1983
- Basic phospholipase A2 from Naja nigricollis snake venom: Phospholipid hydrolysis and effects of electrical and contractile activity of the rat heartToxicology and Applied Pharmacology, 1982
- The morphology of rat soleus neuromuscular junctions treated in vitro with purified β-bungarotoxinBrain Research, 1980
- Deenergization of nerve terminals by β-bungarotoxinBiochemistry, 1978
- The effect of phospholipases and proteases on the binding of γ-aminobutyric acid to junctional complexes of rat cerebellumBiochimica et Biophysica Acta (BBA) - Biomembranes, 1976