Quantitative modelling of interaction of propafenone with sodium channels in cardiac cells
Author:
Publisher
Springer Science and Business Media LLC
Subject
Computer Science Applications,Biomedical Engineering
Link
http://link.springer.com/content/pdf/10.1007/BF02344625.pdf
Reference33 articles.
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2. Balser, J. R. (2001): ‘The cardiac sodium channel: gating function and molecular pharmacology’,J. Mol. Cell. Cardiol.,33, pp. 599–613
3. Benz, I., andKohlhardt, M. (1991): ‘Responsiveness of cardiac Na+ channels to antiarrhythmic drugs: the role of inactivation’,J. Membr. Biol.,122, pp. 267–278
4. Benz, I., andKohlhardt, M. (1994): ‘Chemically modified cardiac Na+ channels and their sensitivity to antiarrhythmics: is there a hidden drug receptor?’,J. Membr. Biol.,139, pp. 191–201
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