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The Journal of General Physiology|January 28, 2004
The Na+ channel inactivation gate is a molecular complex: a novel role of the COOH-terminal domainHoward K Motoike, Huajun Liu, Ian W Glaaser, et al.Nature Communications|March 20, 2012
Perturbation of sodium channel structure by an inherited Long QT Syndrome mutationIan W Glaaser, Jeremiah D Osteen, Akil Puckerin, et al.Channels (Austin, Tex.)|August 19, 2008
A novel LQT-3 mutation disrupts an inactivation gate complex with distinct rate-dependent phenotypic consequencesJohn R Bankston, Kevin J Sampson, Suneel Kateriya, et al.The Journal of General Physiology|December 19, 2025
A critical residue mediates proper assembly and gating of GIRK2 channelsHa Nguyen, Jonathan Mount, Keino Hutchinson, et al.The Journal of General Physiology|July 20, 2017
Dynamic role of the tether helix in PIP2-dependent gating of a G protein-gated potassium channelEmre Lacin, Prafulla Aryal, Ian W Glaaser, et al.Neuroscience Letters|February 5, 2008
Mutation of sodium channel SCN3A in a patient with cryptogenic pediatric partial epilepsyKatherine D Holland, Jennifer A Kearney, Tracy A Glauser, et al.Cell Reports|June 20, 2020
Identification of a G-Protein-Independent Activator of GIRK ChannelsYulin Zhao, Peter Man-Un Ung, Gergely Zahoránszky-Kőhalmi, et al.Pageof 2