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Kir6.2 activation by sulfonylurea receptors: a different mechanism of action for SUR1 and SUR2A subunits via the same residues. , Principalli MA., Physiol Rep. September 1, 2015; 3 (9):
A universally conserved residue in the SUR1 subunit of the KATP channel is essential for translating nucleotide binding at SUR1 into channel opening. , de Wet H., J Physiol. October 15, 2012; 590 (20): 5025-36.
Neurally Derived Tissues in Xenopus laevis Embryos Exhibit a Consistent Bioelectrical Left- Right Asymmetry. , Pai VP ., Stem Cells Int. January 1, 2012; 2012 353491.
Expression of complement components coincides with early patterning and organogenesis in Xenopus laevis. , McLin VA ., Int J Dev Biol. January 1, 2008; 52 (8): 1123-33.
Remodelling of the SUR- Kir6.2 interface of the KATP channel upon ATP binding revealed by the conformational blocker rhodamine 123. , Hosy E., J Physiol. July 1, 2007; 582 (Pt 1): 27-39.
N-terminal transmembrane domain of the SUR controls trafficking and gating of Kir6 channel subunits. , Chan KW., EMBO J. August 1, 2003; 22 (15): 3833-43.
Mutations in the linker domain of NBD2 of SUR inhibit transduction but not nucleotide binding. , Matsuo M., EMBO J. August 15, 2002; 21 (16): 4250-8.
Sulfonylurea receptors inhibit the epithelial sodium channel (ENaC) by reducing surface expression. , Konstas AA., Pflugers Arch. August 1, 2001; 442 (5): 752-61.
Chromanol 293B, a blocker of the slow delayed rectifier K+ current (IKs), inhibits the CFTR Cl- current. , Bachmann A., Naunyn Schmiedebergs Arch Pharmacol. June 1, 2001; 363 (6): 590-6.
Molecular basis for K(ATP) assembly: transmembrane interactions mediate association of a K+ channel with an ABC transporter. , Schwappach B., Neuron. April 1, 2000; 26 (1): 155-67.
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 novel sulfonylurea receptor family member expressed in the embryonic Drosophila dorsal vessel and tracheal system. , Nasonkin I., J Biol Chem. October 8, 1999; 274 (41): 29420-5.
The first-nucleotide binding domain of the cystic-fibrosis transmembrane conductance regulator is important for inhibition of the epithelial Na+ channel. , Schreiber R., Proc Natl Acad Sci U S A. April 27, 1999; 96 (9): 5310-5.
Expression of Xenopus snail in mesoderm and prospective neural fold ectoderm. , Essex LJ., Dev Dyn. October 1, 1993; 198 (2): 108-22.