Open channel block and open channel destabilization: contrasting effects of phenol, TEA+ and local anaesthetics on Kv1.1 K+ channels

Author:

Elliott A.A.,Harrold J.A.,Newman J.P.,Elliott J.R.

Publisher

Elsevier BV

Subject

Toxicology,General Medicine

Reference22 articles.

1. Use-dependent blockers and exit rate of the last ion from the multi-ion pore of a K+ channel;Baukrowitz;Science,1996

2. Closed- and open-state binding of 4-aminopyridine to the cloned human potassium channel Kv1.5;Bouchard;J. Pharmacol. Exp. Ther.,1995

3. Voltage-dependent inhibition of RCK1 K+ channels by phenol, p-cresol, and benzyl alcohol;Elliott;Mol. Pharmacol.,1997

4. The effects of alcohols and other surface-active compounds on neuronal sodium channels;Elliott;Prog. Neurobiol.,1994

5. A beginner's guide to computer simulation of voltage-gated ion conductances;Elliott;Prog. Neurobiol.,1997

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