C.C. Kuo
Department of Physiology
National Taiwan University College of Medicine
Taipei
Taiwan
Name/email consistency: high
- Use-dependent inhibition of the N-methyl-D-aspartate currents by felbamate: a gating modifier with selective binding to the desensitized channels. Kuo, C.C., Lin, B.J., Chang, H.R., Hsieh, C.P. Mol. Pharmacol. (2004)
- Block of tetrodotoxin-resistant Na+ channel pore by multivalent cations: gating modification and Na+ flow dependence. Kuo, C.C., Chen, W.Y., Yang, Y.C. J. Gen. Physiol. (2004)
- Effect of Na(+) flow on Cd(2+) block of tetrodotoxin-resistant Na(+) channels. Kuo, C.C., Lin, T.J., Hsieh, C.P. J. Gen. Physiol. (2002)
- Recovery from inactivation of t-type ca2+ channels in rat thalamic neurons. Kuo, C.C., Yang, S. J. Neurosci. (2001)
- Inhibition of Na(+) current by diphenhydramine and other diphenyl compounds: molecular determinants of selective binding to the inactivated channels. Kuo, C.C., Huang, R.C., Lou, B.S. Mol. Pharmacol. (2000)
- Facilitation of recovery from inactivation by external Na+ and location of the activation gate in neuronal Na+ channels. Kuo, C.C., Liao, S.Y. J. Neurosci. (2000)
- A common anticonvulsant binding site for phenytoin, carbamazepine, and lamotrigine in neuronal Na+ channels. Kuo, C.C. Mol. Pharmacol. (1998)
- Imipramine inhibition of transient K+ current: an external open channel blocker preventing fast inactivation. Kuo, C.C. Biophys. J. (1998)
