1.Enyedi, P. and G. Czirjak, Molecular background of leak K+ currents: two-pore domain potassium channels. Physiol Rev, 2010. 90(2): p. 559-605.
2. Cohen, A., Y. Ben-Abu, and N. Zilberberg, Gating the pore of potassium leak channels. Eur Biophys J, 2009. 39(1): p. 61-73.
3. Dedman, A., et al., The mechano-gated K(2P) channel TREK-1. Eur Biophys J, 2009. 38(3): p. 293-303.
4. Noel, J., G. Sandoz, and F. Lesage, Molecular regulations governing TREK and TRAAK channel functions. Channels (Austin), 2011. 5(5): p. 402-9.
5. Patel, A.J. and E. Honore, 2P domain K+ channels: novel pharmacological targets for volatile general anesthetics. Adv Exp Med Biol, 2003. 536: p. 9-23.
6. Cadaveira-Mosquera, A., et al., Activation of TREK currents by the neuroprotective agent riluzole in mouse sympathetic neurons. J Neurosci, 2011. 31(4): p. 1375-85.
7. Heurteaux, C., et al., Deletion of the background potassium channel TREK-1 results in a depression-resistant phenotype. Nat Neurosci, 2006. 9(9): p. 1134-41.
8. Kennard, L.E., et al., Inhibition of the human two-pore domain potassium channel, TREK-1, by fluoxetine and its metabolite norfluoxetine. Br J Pharmacol, 2005. 144(6): p. 821-9.
9. Bayliss, D.A. and P.Q. Barrett, Emerging roles for two-pore-domain potassium channels and their potential therapeutic impact. Trends Pharmacol Sci, 2008. 29(11): p. 566-75.
10. Es-Salah-Lamoureux, Z., D.F. Steele, and D. Fedida, Research into the therapeutic roles of two-pore-domain potassium channels. Trends Pharmacol Sci, 2010. 31(12): p. 587-95.
11. Mathie, A. and E.L. Veale, Therapeutic potential of neuronal two-pore domain potassium-channel modulators. Curr Opin Investig Drugs, 2007. 8(7): p. 555-62.