Papers associated with inner ear (and dtl)

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	Identification of Aethina tumida Kir Channels as Putative Targets of the Bee Venom Peptide Tertiapin Using Structure-Based Virtual Screening Methods., Doupnik CA., Toxins (Basel). September 19, 2019; 11 (9):
	A valve-like mechanism controls desensitization of functional mammalian isoforms of acid-sensing ion channels., Wu Y., Elife. May 2, 2019; 8
	Expression and Purification of the Pain Receptor TRPV1 for Spectroscopic Analysis., Velisetty P., Sci Rep. August 29, 2017; 7 (1): 9861.
	Ion conduction and selectivity in acid-sensing ion channel 1., Yang L., J Gen Physiol. September 1, 2014; 144 (3): 245-55.
	Three charged amino acids in extracellular loop 1 are involved in maintaining the outer pore architecture of CFTR., Cui G., J Gen Physiol. August 1, 2014; 144 (2): 159-79.
	5-HT3 receptor ion size selectivity is a property of the transmembrane channel, not the cytoplasmic vestibule portals., McKinnon NK., J Gen Physiol. October 1, 2011; 138 (4): 453-66.
	The N terminus of monoamine transporters is a lever required for the action of amphetamines., Sucic S., J Biol Chem. April 2, 2010; 285 (14): 10924-38.
	Molecular basis of inward rectification: polyamine interaction sites located by combined channel and ligand mutagenesis., Kurata HT., J Gen Physiol. November 1, 2004; 124 (5): 541-54.
	Spermine block of the strong inward rectifier potassium channel Kir2.1: dual roles of surface charge screening and pore block., Xie LH., J Gen Physiol. July 1, 2002; 120 (1): 53-66.

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