Papers associated with artery (and kcnj3)

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	Pregnenolone sulfate potentiates the inwardly rectifying K channel Kir2.3., Kobayashi T., PLoS One. July 21, 2009; 4 (7): e6311.
	Differential ion current activation by human 5-HT(1A) receptors in Xenopus oocytes: evidence for agonist-directed trafficking of receptor signalling., Heusler P., Neuropharmacology. December 1, 2005; 49 (7): 963-76.
	Tertiapin-Q blocks recombinant and native large conductance K+ channels in a use-dependent manner., Kanjhan R., J Pharmacol Exp Ther. September 1, 2005; 314 (3): 1353-61.
	Effects of ginsenoside on G protein-coupled inwardly rectifying K+ channel activity expressed in Xenopus oocytes., Choi S., Eur J Pharmacol. May 9, 2003; 468 (2): 83-92.
	The Orphan G protein-coupled receptors GPR41 and GPR43 are activated by propionate and other short chain carboxylic acids., Brown AJ., J Biol Chem. March 28, 2003; 278 (13): 11312-9.
	Distinct sites on G protein beta gamma subunits regulate different effector functions., Mirshahi T., J Biol Chem. September 27, 2002; 277 (39): 36345-50.
	Functional expression of a novel ginsenoside Rf binding protein from rat brain mRNA in Xenopus laevis oocytes., Choi S., Mol Pharmacol. April 1, 2002; 61 (4): 928-35.
	Identification of melanin concentrating hormone (MCH) as the natural ligand for the orphan somatostatin-like receptor 1 (SLC-1)., Bächner D., FEBS Lett. September 3, 1999; 457 (3): 522-4.
	Positive and negative coupling of the metabotropic glutamate receptors to a G protein-activated K+ channel, GIRK, in Xenopus oocytes., Sharon D., J Gen Physiol. April 1, 1997; 109 (4): 477-90.

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