Characterization of drug binding within the HCN1 channel pore
Author:
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/s41598-018-37116-2.pdf
Reference91 articles.
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3. Vemana, S., Pandey, S. & Larsson, H. P. S4 movement in a mammalian HCN channel. J Gen Physiol 123, 21–32, https://doi.org/10.1085/jgp.200308916 (2004).
4. Biel, M., Wahl-Schott, C., Michalakis, S. & Zong, X. Hyperpolarization-activated cation channels: from genes to function. Physiological reviews 89, 847–885, https://doi.org/10.1152/physrev.00029.2008 (2009).
5. Ishii, T. M., Takano, M., Xie, L. H., Noma, A. & Ohmori, H. Molecular characterization of the hyperpolarization-activated cation channel in rabbit heart sinoatrial node. J Biol Chem 274, 12835–12839 (1999).
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