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.
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A C-terminal motif found in the beta2-adrenergic receptor, P2Y1 receptor and cystic fibrosis transmembrane conductance regulator determines binding to the Na+/H+ exchanger regulatory factor family of PDZ proteinsDefective regulation of gap junctional coupling in cystic fibrosis pancreatic duct cellsInhibition of cystic fibrosis transmembrane conductance regulator by novel interaction with the metabolic sensor AMP-activated protein kinaseAssembly and trafficking of a multiprotein ROMK (Kir 1.1) channel complex by PDZ interactionsChloride channels: an emerging molecular pictureRegulation of ROMK1 channels by protein-tyrosine kinase and -tyrosine phosphataseMouse cystic fibrosis transmembrane conductance regulator forms cAMP-PKA-regulated apical chloride channels in cortical collecting ductInvestigating CFTR and KCa3.1 Protein/Protein InteractionsThe cystic fibrosis transmembrane conductance regulator activates aquaporin 3 in airway epithelial cells.Rat homolog of sulfonylurea receptor 2B determines glibenclamide sensitivity of ROMK2 in Xenopus laevis oocyte.Protein kinase C (PKC)-induced phosphorylation of ROMK1 is essential for the surface expression of ROMK1 channelsA hyperprostaglandin E syndrome mutation in Kir1.1 (renal outer medullary potassium) channels reveals a crucial residue for channel function in Kir1.3 channels.CFTR modulates programmed cell death by decreasing intracellular pH in Chinese hamster lung fibroblasts.CFTR and TNR-CFTR expression and function in the kidney.Regulation of ROMK (Kir1.1) channels: new mechanisms and aspects.The pathophysiological and molecular basis of Bartter's and Gitelman's syndromes.Molecular diversity and regulation of renal potassium channels.Evidence for the existence of a sulfonylurea-receptor-like protein in plants: modulation of stomatal movements and guard cell potassium channels by sulfonylureas and potassium channel openers.Regulation of the ROMK channel: interaction of the ROMK with associate proteins.Ion channels and the control of blood pressure.Nucleotides and phospholipids compete for binding to the C terminus of KATP channels.Gating of inward-rectifier K+ channels by intracellular pH.The cystic fibrosis transmembrane regulator (CFTR) in the kidney.Cystic fibrosis transmembrane conductance regulator and the outwardly rectifying chloride channel: a relationship between two chloride channels expressed in epithelial cells.Renal tubule potassium channels: function, regulation and structure.The glycolytic enzymes glyceraldehyde 3-phosphate dehydrogenase and enolase interact with the renal epithelial K+ channel ROMK2 and regulate its function.Potassium transport in the mammalian collecting duct.Functional interaction between CFTR and the sodium-phosphate co-transport type 2a in Xenopus laevis oocytesCFTR chloride channel in the apical compartments: spatiotemporal coupling to its interacting partners.The hypertonic environment differentially regulates wild-type CFTR and TNR-CFTR chloride channels.Glyburide is anti-inflammatory and associated with reduced mortality in melioidosis.Chloride channels in the kidney: lessons learned from knockout animals.ABCA1: regulation, trafficking and association with heteromeric proteins.Analysis of CFTR interactome in the macromolecular complexes.Continuous detection of extracellular ATP on living cells by using atomic force microscopyProperties of an inwardly rectifying ATP-sensitive K+ channel in the basolateral membrane of renal proximal tubuleIon channels: function unravelled by dysfunction.Chloride channel and chloride conductance regulator domains of CFTR, the cystic fibrosis transmembrane conductance regulator.Salt handling in the distal nephron: lessons learned from inherited human disorders.Chloride channel diseases resulting from impaired transepithelial transport or vesicular function
P2860
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P2860
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.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on July 1996
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Sensitivity of a renal K+ chan ...... rosis transmembrane regulator.
@en
Sensitivity of a renal K+ channel
@nl
type
label
Sensitivity of a renal K+ chan ...... rosis transmembrane regulator.
@en
Sensitivity of a renal K+ channel
@nl
prefLabel
Sensitivity of a renal K+ chan ...... rosis transmembrane regulator.
@en
Sensitivity of a renal K+ channel
@nl
P2093
P2860
P356
P1476
Sensitivity of a renal K+ chan ...... rosis transmembrane regulator.
@en
P2093
C M McNicholas
E M Schwiebert
G Giebisch
S C Hebert
W B Guggino
P2860
P304
P356
10.1073/PNAS.93.15.8083
P407
P577
1996-07-01T00:00:00Z