Papers associated with peripheral nervous system (and kcnj6)

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	Conformational changes underlying pore dilation in the cytoplasmic domain of mammalian inward rectifier K+ channels., Inanobe A., PLoS One. January 1, 2013; 8 (11): e79844.
	Intron 4 containing novel GABAB1 isoforms impair GABAB receptor function., Lee C, Lee C., PLoS One. November 16, 2010; 5 (11): e14044.
	Inhibition of G-protein-activated inwardly rectifying K+ channels by the selective norepinephrine reuptake inhibitors atomoxetine and reboxetine., Kobayashi T., Neuropsychopharmacology. June 1, 2010; 35 (7): 1560-9.
	Pregnenolone sulfate potentiates the inwardly rectifying K channel Kir2.3., Kobayashi T., PLoS One. July 21, 2009; 4 (7): e6311.
	Divergent regulation of GIRK1 and GIRK2 subunits of the neuronal G protein gated K+ channel by GalphaiGDP and Gbetagamma., Rubinstein M., J Physiol. July 15, 2009; 587 (Pt 14): 3473-91.
	Inhibition of G protein-activated inwardly rectifying K+ channels by ifenprodil., Kobayashi T., Neuropsychopharmacology. March 1, 2006; 31 (3): 516-24.
	G protein-activated inwardly rectifying K+ channel inhibition and rescue of weaver mouse motor functions by antidepressants., Takahashi T., Neurosci Res. February 1, 2006; 54 (2): 104-11.
	Modulators of G protein-activated inwardly rectifying K+ channels: potentially therapeutic agents for addictive drug users., Kobayashi T., Ann N Y Acad Sci. October 1, 2004; 1025 590-4.
	Inhibition of G protein-activated inwardly rectifying K+ channels by various antidepressant drugs., Kobayashi T., Neuropsychopharmacology. October 1, 2004; 29 (10): 1841-51.
	The sensitivity of G protein-activated K+ channels toward halothane is essentially determined by the C terminus., Milovic S., J Biol Chem. August 13, 2004; 279 (33): 34240-9.
	Evolving potassium channels by means of yeast selection reveals structural elements important for selectivity., Bichet D., Proc Natl Acad Sci U S A. March 30, 2004; 101 (13): 4441-6.
	betaL-betaM loop in the C-terminal domain of G protein-activated inwardly rectifying K(+) channels is important for G(betagamma) subunit activation., Finley M., J Physiol. March 16, 2004; 555 (Pt 3): 643-57.
	Inhibition of G protein-activated inwardly rectifying K+ channels by fluoxetine (Prozac)., Kobayashi T., Br J Pharmacol. March 1, 2003; 138 (6): 1119-28.
	Serine 329 of the mu-opioid receptor interacts differently with agonists., Pil J., J Pharmacol Exp Ther. March 1, 2003; 304 (3): 924-30.

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