The use of peptide-membrane interactions in the design of selective and potent sodium channel inhibitors
Schroeder, Christina, Agwa, Akello, Mueller, Alexander, Chow, Chun Yuen, Peigneur, Steve, Lawrence, Nicole, Deplazes, Evelyne, Mark, Alan, Craik, David, Tytgat, Jan, King, Glenn, Vetter, Irina and Henriques, Sonia Troeira (2018). The use of peptide-membrane interactions in the design of selective and potent sodium channel inhibitors. 35th European Peptide Symposium, Dublin City University, Ireland, 26-31 August 2018. Oxford, United Kingdom: John Wiley & Sons.
Bibic, L., Herzig, V., King, G. F., Ma, L., Chow, C. Y. and Stokes, L. (2018). Bug off pain: probing P2X channels with venoms. Purines 2018 Basic and Translational Science on Purinergic Signaling and its Components for a Healthy and Better World, Foz do Iguaçu, Brazil, 19-22 June 2018. Dordrecht, Netherlands: Springer.
Novel Human Eag Channel Antagonists from Spider Venoms
Ma, Linlin, Chin, Yanni K., Dekan, Zoltan, Ikonomopoulou, Maria, Herzig, Volker, Chow, Chun Yuen, Alewood, Paul and King, Glenn F. (2017). Novel Human Eag Channel Antagonists from Spider Venoms. 58th Annual Meeting of the Biophysical-Society, San Francisco, CA, United States, 15-19 February 2014. St. Louis, MO 63146 United States: Cell Press. doi: 10.1016/j.bpj.2016.11.1800
Three peptide modulators of the human voltage-gated sodium channel 1.7, an important analgesic target, from venom of an Australian tarantula
Chow, Chun Yuen, Cristofori-Armstrong, Ben, Undheim, Eivind A. B., King, Glenn F. and Rash, Lachlan D. (2015). Three peptide modulators of the human voltage-gated sodium channel 1.7, an important analgesic target, from venom of an Australian tarantula. Toxins, 7 (7), 2494-2513. doi: 10.3390/toxins7072494
