相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。Extracellular potassium dependency of block of HERG by quinidine and cisapride is primarily determined by the permeant ion and not by inactivation.
Brad Barrows et al.
Channels (2010)
The Membrane-Bound State of K2P Potassium Channels
Werner Treptow et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2010)
A structural model for K2P potassium channels based on 23 pairs of interacting sites and continuum electrostatics
Astrid Kollewe et al.
JOURNAL OF GENERAL PHYSIOLOGY (2009)
TWIK-related acid-sensitive K+ channel 1 (TASK1) and TASK3 critically influence T lymphocyte effector functions
Sven G. Meuth et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2008)
A role for TASK-1 (KCNK3) channels in the chemosensory control of breathing
Stefan Trapp et al.
JOURNAL OF NEUROSCIENCE (2008)
Reciprocal modulation of Ih and ITASK in thalamocortical relay neurons by halothane
Thomas Budde et al.
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY (2008)
Atomic structure of a voltage-dependent K+ channel in a lipid membrane-like environment
Stephen B. Long et al.
NATURE (2007)
The acid-sensitive potassium channel TASK-1 in rat cardiac muscle
Caroline Putzke et al.
CARDIOVASCULAR RESEARCH (2007)
Chromanol 293B binding in KCNQ1 (Kv7.1) channels involves electrostatic interactions with a potassium ion in the selectivity filter
Christian Lerche et al.
MOLECULAR PHARMACOLOGY (2007)
Monte Carlo-energy minimization of correolide in the Kv1.3 channel: possible role of potassium ion in ligand-receptor interactions
Iva Bruhova et al.
BMC STRUCTURAL BIOLOGY (2007)
Mechanism of intracellular block of the KcsA K+ channel by tetrabutylammonium:: Insights from X-ray crystallography, electrophysiology and replica-exchange molecular dynamics simulations
Jose D. Faraldo-Gomez et al.
JOURNAL OF MOLECULAR BIOLOGY (2007)
Comparison of potent Kv1.5 potassium channel inhibitors reveals the molecular basis for blocking kinetics and binding mode
Nathalie Strutz-Seebohm et al.
CELLULAR PHYSIOLOGY AND BIOCHEMISTRY (2007)
Binding site of a novel Kv1.5 blocker: A foot in the door against atrial fibrillation
Niels Decher et al.
MOLECULAR PHARMACOLOGY (2006)
The pore helix dipole has a minor role in inward rectifier channel function
FC Chatelain et al.
NEURON (2005)
Molecular determinants of frequency dependence and Ca2+ potentiation of verapamil block in the pore region of Cav1.2
N Dilmac et al.
MOLECULAR PHARMACOLOGY (2004)
Crystal structure of the potassium channel KirBac1.1 in the closed state
AL Kuo et al.
SCIENCE (2003)
Position of aromatic residues in the S6 domain, not inactivation, dictates cisapride sensitivity of HERG and eag potassium channels
J Chen et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2002)
TASK-5, a novel member of the tandem pore K+ channel family
I Ashmole et al.
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY (2001)
Characterization of TASK-4, a novel member of the pH-sensitive, two-pore domain potassium channel family
N Decher et al.
FEBS LETTERS (2001)
Functional characterisation of human TASK-3, an acid-sensitive two-pore domain potassium channel
HJ Meadows et al.
NEUROPHARMACOLOGY (2001)
The endocannabinoid anandamide is a direct and selective blocker of the background K+ channel TASK-1
F Maingret et al.
EMBO JOURNAL (2001)
A structural basis for drug-induced long QT syndrome
JS Mitcheson et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2000)
TASK-3, a novel tandem pore domain acid-sensitive K+ channel -: An extracellular histidine as pH sensor
S Rajan et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2000)
TASK (TWIK-related acid-sensitive K+ channel) is expressed in glomerulosa cells of rat adrenal cortex and inhibited by angiotensin II
G Czirják et al.
MOLECULAR ENDOCRINOLOGY (2000)