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Disease progression and search for monogenic diabetes among children with new onset type 1 diabetes negative for ICA, GAD- and IA-2 Antibodies. , Pörksen S., BMC Endocr Disord. September 23, 2010; 10 16.
Functional analysis of two Kir6.2 ( KCNJ11) mutations, K170T and E322K, causing neonatal diabetes. , Tarasov AI., Diabetes Obes Metab. November 1, 2007; 9 Suppl 2 46-55.
Iptakalim, a vascular ATP-sensitive potassium (KATP) channel opener, closes rat pancreatic beta-cell KATP channels and increases insulin release. , Misaki N., J Pharmacol Exp Ther. August 1, 2007; 322 (2): 871-8.
Scavenging of 14-3-3 proteins reveals their involvement in the cell-surface transport of ATP-sensitive K+ channels. , Heusser K., J Cell Sci. October 15, 2006; 119 (Pt 20): 4353-63.
Functional effects of naturally occurring KCNJ11 mutations causing neonatal diabetes on cloned cardiac KATP channels. , Tammaro P., J Physiol. February 15, 2006; 571 (Pt 1): 3-14.
The novel diazoxide analog 3-isopropylamino-7-methoxy-4H-1,2,4-benzothiadiazine 1,1-dioxide is a selective Kir6.2/ SUR1 channel opener. , Dabrowski M., Diabetes. June 1, 2002; 51 (6): 1896-906.
Structural basis for the interference between nicorandil and sulfonylurea action. , Reimann F., Diabetes. October 1, 2001; 50 (10): 2253-9.
Glimepiride block of cloned beta-cell, cardiac and smooth muscle K(ATP) channels. , Song DK., Br J Pharmacol. May 1, 2001; 133 (1): 193-9.
Effects of mitiglinide (S 21403) on Kir6.2/ SUR1, Kir6.2/ SUR2A and Kir6.2/SUR2B types of ATP-sensitive potassium channel. , Reimann F., Br J Pharmacol. April 1, 2001; 132 (7): 1542-8.
Nucleotide modulation of pinacidil stimulation of the cloned K(ATP) channel Kir6.2/ SUR2A. , Gribble FM., Mol Pharmacol. June 1, 2000; 57 (6): 1256-61.
Altered functional properties of KATP channel conferred by a novel splice variant of SUR1. , Sakura H., J Physiol. December 1, 1999; 521 Pt 2 337-50.
In vitro mechanism of action on insulin release of S-22068, a new putative antidiabetic compound. , Le Brigand L., Br J Pharmacol. November 1, 1999; 128 (5): 1021-6.
Interaction of vanadate with the cloned beta cell K(ATP) channel. , Proks P., J Biol Chem. September 3, 1999; 274 (36): 25393-7.
Differential sensitivity of beta-cell and extrapancreatic K(ATP) channels to gliclazide. , Gribble FM., Diabetologia. July 1, 1999; 42 (7): 845-8.
KATP channel inhibition by ATP requires distinct functional domains of the cytoplasmic C terminus of the pore-forming subunit. , Drain P., Proc Natl Acad Sci U S A. November 10, 1998; 95 (23): 13953-8.
Mechanism of cloned ATP-sensitive potassium channel activation by oleoyl-CoA. , Gribble 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., J Gen Physiol. September 1, 1998; 112 (3): 333-49.
Mechanism of ATP-sensitive K channel inhibition by sulfhydryl modification. , Trapp S., 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., 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., 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., 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., Proc Natl Acad Sci U S A. August 5, 1997; 94 (16): 8872-7.
Properties of cloned ATP-sensitive K+ currents expressed in Xenopus oocytes. , Gribble 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., Diabetologia. October 1, 1996; 39 (10): 1233-6.