Papers associated with kcnj11

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	Mechanism of cloned ATP-sensitive potassium channel activation by oleoyl-CoA., Gribble FM, Proks P, Corkey BE, Ashcroft FM., J Biol Chem. October 9, 1998; 273 (41): 26383-7.
	Molecular analysis of ATP-sensitive K channel gating and implications for channel inhibition by ATP., Trapp S, Proks P, Tucker SJ, Ashcroft FM., J Gen Physiol. September 1, 1998; 112 (3): 333-49.
	Mechanism of ATP-sensitive K channel inhibition by sulfhydryl modification., Trapp S, Tucker SJ, Ashcroft FM., J Gen Physiol. September 1, 1998; 112 (3): 325-32.
	MgATP activates the beta cell KATP channel by interaction with its SUR1 subunit., Gribble FM, Tucker SJ, Haug T, Ashcroft FM., Proc Natl Acad Sci U S A. June 9, 1998; 95 (12): 7185-90.
	Phentolamine block of KATP channels is mediated by Kir6.2., Proks P, Ashcroft FM., Proc Natl Acad Sci U S A. October 14, 1997; 94 (21): 11716-20.
	The interaction of nucleotides with the tolbutamide block of cloned ATP-sensitive K+ channel currents expressed in Xenopus oocytes: a reinterpretation., Gribble FM, Tucker SJ, Ashcroft FM., J Physiol. October 1, 1997; 504 ( Pt 1) 35-45.
	Activation and inhibition of K-ATP currents by guanine nucleotides is mediated by different channel subunits., Trapp S, Tucker SJ, Ashcroft FM., Proc Natl Acad Sci U S A. August 5, 1997; 94 (16): 8872-7.
	Truncation of Kir6.2 produces ATP-sensitive K+ channels in the absence of the sulphonylurea receptor., Tucker SJ, Gribble FM, Zhao C, Trapp S, Ashcroft FM., Nature. May 8, 1997; 387 (6629): 179-83.
	Properties of cloned ATP-sensitive K+ currents expressed in Xenopus oocytes., Gribble FM, Ashfield R, Ammälä C, Ashcroft FM., J Physiol. January 1, 1997; 498 ( Pt 1) 87-98.
	Sequence variations in the human Kir6.2 gene, a subunit of the beta-cell ATP-sensitive K-channel: no association with NIDDM in while Caucasian subjects or evidence of abnormal function when expressed in vitro., Sakura H, Wat N, Horton V, Millns H, Turner RC, Ashcroft FM., Diabetologia. October 1, 1996; 39 (10): 1233-6.
	Molecular site for nucleotide binding on an ATP-sensitive renal K+ channel (ROMK2)., McNicholas CM, Yang Y, Giebisch G, Hebert SC., Am J Physiol. August 1, 1996; 271 (2 Pt 2): F275-85.
	Sensitivity of a renal K+ channel (ROMK2) to the inhibitory sulfonylurea compound glibenclamide is enhanced by coexpression with the ATP-binding cassette transporter cystic fibrosis transmembrane regulator., McNicholas CM, Guggino WB, Schwiebert EM, Hebert SC, Giebisch G, Egan ME., Proc Natl Acad Sci U S A. July 23, 1996; 93 (15): 8083-8.

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