Papers associated with limb (and kcnj1)

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	Tamm-Horsfall glycoprotein interacts with renal outer medullary potassium channel ROMK2 and regulates its function., Renigunta A., J Biol Chem. January 21, 2011; 286 (3): 2224-35.
	The glycolytic enzymes glyceraldehyde 3-phosphate dehydrogenase and enolase interact with the renal epithelial K+ channel ROMK2 and regulate its function., Renigunta A., Cell Physiol Biochem. January 1, 2011; 28 (4): 663-72.
	Organization of the pronephric kidney revealed by large-scale gene expression mapping., Raciti D., Genome Biol. January 1, 2008; 9 (5): R84.
	H bonding at the helix-bundle crossing controls gating in Kir potassium channels., Rapedius M., Neuron. August 16, 2007; 55 (4): 602-14.
	Moving the pH gate of the Kir1.1 inward rectifier channel., Nanazashvili M., Channels (Austin). January 1, 2007; 1 (1): 21-8.
	CFTR is required for PKA-regulated ATP sensitivity of Kir1.1 potassium channels in mouse kidney., Lu M., J Clin Invest. March 1, 2006; 116 (3): 797-807.
	Apical localization of renal K channel was not altered in mutant WNK4 transgenic mice., Yamauchi K., Biochem Biophys Res Commun. July 8, 2005; 332 (3): 750-5.
	Structural locus of the pH gate in the Kir1.1 inward rectifier channel., Sackin H., Biophys J. April 1, 2005; 88 (4): 2597-606.
	Mechanism of rectification in inward-rectifier K+ channels., Guo D., J Gen Physiol. April 1, 2003; 121 (4): 261-75.
	The serum and glucocorticoid-inducible kinase SGK1 and the Na+/H+ exchange regulating factor NHERF2 synergize to stimulate the renal outer medullary K+ channel ROMK1., Yun CC., J Am Soc Nephrol. December 1, 2002; 13 (12): 2823-30.
	Functional implications of mutations in the human renal outer medullary potassium channel (ROMK2) identified in Bartter syndrome., Starremans PG., Pflugers Arch. January 1, 2002; 443 (3): 466-72.
	Mechanism underlying bupivacaine inhibition of G protein-gated inwardly rectifying K+ channels., Zhou W., Proc Natl Acad Sci U S A. May 22, 2001; 98 (11): 6482-7.
	Rat homolog of sulfonylurea receptor 2B determines glibenclamide sensitivity of ROMK2 in Xenopus laevis oocyte., Tanemoto M., Am J Physiol Renal Physiol. April 1, 2000; 278 (4): F659-66.
	A Bartter's syndrome mutation of ROMK1 exerts dominant negative effects on K(+) conductance., Kunzelmann K., Cell Physiol Biochem. January 1, 2000; 10 (3): 117-24.
	Regulation of the ROMK potassium channel in the kidney., Wald H., Exp Nephrol. January 1, 1999; 7 (3): 201-6.
	Localization of ROMK channels in the rat kidney., Mennitt PA., J Am Soc Nephrol. December 1, 1997; 8 (12): 1823-30.
	A conserved cytoplasmic region of ROMK modulates pH sensitivity, conductance, and gating., Choe H., Am J Physiol. October 1, 1997; 273 (4): F516-29.
	Arachidonic acid inhibits activity of cloned renal K+ channel, ROMK1., Macica CM., Am J Physiol. September 1, 1996; 271 (3 Pt 2): F588-94.
	Susceptibility of cloned K+ channels to reactive oxygen species., Duprat F., Proc Natl Acad Sci U S A. December 5, 1995; 92 (25): 11796-800.
	Cloning provides evidence for a family of inward rectifier and G-protein coupled K+ channels in the brain., Lesage F., FEBS Lett. October 10, 1994; 353 (1): 37-42.

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