scholarly article | Q13442814 |
P50 | author | Nikita Gamper | Q41275613 |
P2093 | author name string | Yang Li | |
Mark S Shapiro | |||
P2860 | cites work | KCNQ2 and KCNQ3 potassium channel subunits: molecular correlates of the M-channel | Q22008501 |
KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafness | Q22008780 | ||
A constitutively open potassium channel formed by KCNQ1 and KCNE3 | Q22011154 | ||
Molecular cloning and functional expression of KCNQ5, a potassium channel subunit that may contribute to neuronal M-current diversity | Q22254006 | ||
Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias | Q24311437 | ||
Coassembly of K(V)LQT1 and minK (IsK) proteins to form cardiac I(Ks) potassium channel | Q24318271 | ||
A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome | Q24318498 | ||
A carboxy-terminal domain determines the subunit specificity of KCNQ K+ channel assembly | Q24534565 | ||
Receptor-induced transient reduction in plasma membrane PtdIns(4,5)P2 concentration monitored in living cells | Q74344711 | ||
Phosphatidylinositol 4,5-bisphosphate functions as a second messenger that regulates cytoskeleton-plasma membrane adhesion | Q27939824 | ||
The novel anticonvulsant retigabine activates M-currents in Chinese hamster ovary-cells tranfected with human KCNQ2/3 subunits | Q28138343 | ||
Retigabine, a novel anti-convulsant, enhances activation of KCNQ2/Q3 potassium channels | Q28144303 | ||
KCNQ5, a novel potassium channel broadly expressed in brain, mediates M-type currents | Q28144661 | ||
Reconstitution of muscarinic modulation of the KCNQ2/KCNQ3 K(+) channels that underlie the neuronal M current | Q28145290 | ||
International Union of Pharmacology. XLI. Compendium of voltage-gated ion channels: potassium channels | Q28189496 | ||
The identification and characterization of a noncontinuous calmodulin-binding site in noninactivating voltage-dependent KCNQ potassium channels | Q28198311 | ||
K(V)LQT1 and lsK (minK) proteins associate to form the I(Ks) cardiac potassium current | Q28295470 | ||
Calmodulin is an auxiliary subunit of KCNQ2/3 potassium channels | Q28511803 | ||
Imaging actin and dynamin recruitment during invagination of single clathrin-coated pits | Q29620473 | ||
A real-time view of life within 100 nm of the plasma membrane | Q31890399 | ||
KCNQ potassium channels: physiology, pathophysiology, and pharmacology | Q34305841 | ||
Genes and mutations in idiopathic epilepsy | Q34386799 | ||
Emerging structure of the nicotinic acetylcholine receptors | Q34522883 | ||
Secretory granules are recaptured largely intact after stimulated exocytosis in cultured endocrine cells. | Q34763388 | ||
Calmodulin mediates Ca2+-dependent modulation of M-type K+ channels | Q36447189 | ||
Bradykinin excites rat sympathetic neurons by inhibition of M current through a mechanism involving B2 receptors and G alpha q/11. | Q38299056 | ||
M-channel gating and simulation | Q40147110 | ||
Total internal reflection fluorescence | Q40181869 | ||
Activation of KCNQ5 channels stably expressed in HEK293 cells by BMS-204352. | Q40745093 | ||
KCNQ4 channel activation by BMS-204352 and retigabine | Q40802799 | ||
Mechanisms underlying modulation of neuronal KCNQ2/KCNQ3 potassium channels by extracellular protons | Q41939192 | ||
M channel KCNQ2 subunits are localized to key sites for control of neuronal network oscillations and synchronization in mouse brain. | Q42513993 | ||
Antibodies and a cysteine-modifying reagent show correspondence of M current in neurons to KCNQ2 and KCNQ3 K+ channels | Q43263581 | ||
Activation of expressed KCNQ potassium currents and native neuronal M-type potassium currents by the anti-convulsant drug retigabine. | Q43683699 | ||
Recovery from muscarinic modulation of M current channels requires phosphatidylinositol 4,5-bisphosphate synthesis | Q44092262 | ||
Molecular correlates of the M-current in cultured rat hippocampal neurons | Q44161111 | ||
Subunit-specific modulation of KCNQ potassium channels by Src tyrosine kinase. | Q44270181 | ||
PIP(2) activates KCNQ channels, and its hydrolysis underlies receptor-mediated inhibition of M currents | Q44386912 | ||
Effect of the KCNQ potassium channel opener retigabine on single KCNQ2/3 channels expressed in CHO cells | Q44408542 | ||
(S)-N-[1-(3-morpholin-4-ylphenyl)ethyl]- 3-phenylacrylamide: an orally bioavailable KCNQ2 opener with significant activity in a cortical spreading depression model of migraine | Q44507857 | ||
Direct activation of the epithelial Na(+) channel by phosphatidylinositol 3,4,5-trisphosphate and phosphatidylinositol 3,4-bisphosphate produced by phosphoinositide 3-OH kinase | Q47930919 | ||
Two new potent neurotransmitter release enhancers, 10,10-bis(4-pyridinylmethyl)-9(10H)-anthracenone and 10,10-bis(2-fluoro-4-pyridinylmethyl)-9(10H)-anthracenone: comparison to linopirdine | Q48473252 | ||
C-terminal interaction of KCNQ2 and KCNQ3 K+ channels | Q48831806 | ||
Interdomain interactions underlying activation of cyclic nucleotide-gated channels. | Q52527323 | ||
Inhibition of the muscarinic receptor-activated K+ current by N-ethylmaleimide in rabbit heart | Q67988107 | ||
Modulation of Ca2+ channels by PTX-sensitive G-proteins is blocked by N-ethylmaleimide in rat sympathetic neurons | Q71657344 | ||
Total internal reflection fluorescence microscopy in cell biology | Q73096752 | ||
Blocker protection in the pore of a voltage-gated K+ channel and its structural implications | Q73412357 | ||
Properties of single M-type KCNQ2/KCNQ3 potassium channels expressed in mammalian cells | Q74120884 | ||
P433 | issue | 22 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 5079-5090 | |
P577 | publication date | 2004-06-01 | |
P1433 | published in | Journal of Neuroscience | Q1709864 |
P1476 | title | Single-channel analysis of KCNQ K+ channels reveals the mechanism of augmentation by a cysteine-modifying reagent | |
P478 | volume | 24 |
Q36843204 | A carboxy-terminal inter-helix linker as the site of phosphatidylinositol 4,5-bisphosphate action on Kv7 (M-type) K+ channels. |
Q46947143 | A spontaneous mutation involving Kcnq2 (Kv7.2) reduces M-current density and spike frequency adaptation in mouse CA1 neurons. |
Q37402286 | Affinity for phosphatidylinositol 4,5-bisphosphate determines muscarinic agonist sensitivity of Kv7 K+ channels |
Q42619127 | Atypical gating of M-type potassium channels conferred by mutations in uncharged residues in the S4 region of KCNQ2 causing benign familial neonatal convulsions. |
Q30480033 | Ca2+/calmodulin disrupts AKAP79/150 interactions with KCNQ (M-Type) K+ channels |
Q54229916 | Cholinergic signalling-regulated KV7.5 currents are expressed in colonic ICC-IM but not ICC-MP. |
Q36498532 | Combinatorial augmentation of voltage-gated KCNQ potassium channels by chemical openers |
Q33744493 | Depolarization increases phosphatidylinositol (PI) 4,5-bisphosphate level and KCNQ currents through PI 4-kinase mechanisms |
Q30484864 | Determinants within the turret and pore-loop domains of KCNQ3 K+ channels governing functional activity. |
Q42032547 | Direct modulation of TRPM4 and TRPM3 channels by the phospholipase C inhibitor U73122. |
Q33401229 | Discovery of a novel activator of KCNQ1-KCNE1 K channel complexes |
Q27023978 | Driving with no brakes: molecular pathophysiology of Kv7 potassium channels |
Q28575228 | Dual phosphorylations underlie modulation of unitary KCNQ K(+) channels by Src tyrosine kinase |
Q35849402 | Effects of KCNQ channel modulators on the M-type potassium current in primate retinal pigment epithelium. |
Q34972352 | Effects of KCNQ2 gene truncation on M-type Kv7 potassium currents |
Q35644862 | G-protein βγ subunits are positive regulators of Kv7.4 and native vascular Kv7 channel activity. |
Q36838876 | Gating consequences of charge neutralization of arginine residues in the S4 segment of K(v)7.2, an epilepsy-linked K+ channel subunit |
Q35843838 | Gating currents from Kv7 channels carrying neuronal hyperexcitability mutations in the voltage-sensing domain. |
Q30485406 | Homomeric and heteromeric assembly of KCNQ (Kv7) K+ channels assayed by total internal reflection fluorescence/fluorescence resonance energy transfer and patch clamp analysis |
Q28284500 | IKs channels open slowly because KCNE1 accessory subunits slow the movement of S4 voltage sensors in KCNQ1 pore-forming subunits |
Q24676507 | Inactivation as a new regulatory mechanism for neuronal Kv7 channels |
Q43024045 | Inhibitory role of phosphatidylinositol 4,5-bisphosphate on TMEM16A-encoded calcium-activated chloride channels in rat pulmonary artery. |
Q48112896 | Intracellular zinc activates KCNQ channels by reducing their dependence on phosphatidylinositol 4,5-bisphosphate |
Q26774667 | KCNQ potassium channels in sensory system and neural circuits |
Q64122292 | KCNQ/M-channels regulate mouse vagal bronchopulmonary C-fiber excitability and cough sensitivity |
Q35543305 | KCNQ5/K(v)7.5 potassium channel expression and subcellular localization in primate retinal pigment epithelium and neural retina |
Q79782370 | L-Arginine currents in rat cardiac ventricular myocytes |
Q64079484 | Mechanisms of cannabinoid CB receptor-mediated reduction of dopamine neuronal excitability in mouse ventral tegmental area |
Q39066787 | Mg²⁺ modulation of the single-channel properties of KCa3.1 in human erythroleukemia cells |
Q36823889 | N-ethylmaleimide activates a Cl(-)-independent component of K(+) flux in mouse erythrocytes |
Q92165160 | Neuropathic pain and Kv7 voltage-gated potassium channels: The potential role of Kv7 activators in the treatment of neuropathic pain |
Q35102221 | Oxidative modification of M-type K(+) channels as a mechanism of cytoprotective neuronal silencing |
Q34464180 | Pathways modulating neural KCNQ/M (Kv7) potassium channels |
Q29303618 | Phospholipase C in Living Cells |
Q36010857 | Pore helix-S6 interactions are critical in governing current amplitudes of KCNQ3 K+ channels |
Q37362041 | Potassium channels in peripheral pain pathways: expression, function and therapeutic potential |
Q35068102 | Redox and nitric oxide-mediated regulation of sensory neuron ion channel function |
Q42424237 | Regions of KCNQ K(+) channels controlling functional expression |
Q46776132 | Regulation of Kv7 (KCNQ) K+ channel open probability by phosphatidylinositol 4,5-bisphosphate. |
Q80065013 | Regulation of M(Kv7.2/7.3) channels in neurons by PIP(2) and products of PIP(2) hydrolysis: significance for receptor-mediated inhibition |
Q36986504 | Regulation of ion transport proteins by membrane phosphoinositides |
Q37073174 | Regulation of neural KCNQ channels: signalling pathways, structural motifs and functional implications |
Q34317893 | Specification of skeletal muscle differentiation by repressor element-1 silencing transcription factor (REST)-regulated Kv7.4 potassium channels |
Q33911083 | Structural requirements for differential sensitivity of KCNQ K+ channels to modulation by Ca2+/calmodulin |
Q27675217 | Structure of a Ca2+/CaM:Kv7.4 (KCNQ4) B-Helix Complex Provides Insight into M Current Modulation |
Q36782546 | Target-specific PIP(2) signalling: how might it work? |
Q33933223 | The KCNQ5 potassium channel mediates a component of the afterhyperpolarization current in mouse hippocampus |
Q90399746 | The KV 7 channel activator retigabine suppresses mouse urinary bladder afferent nerve activity without affecting detrusor smooth muscle K+ channel currents |
Q35874979 | The Role of the Carboxyl Terminus Helix C-D Linker in Regulating KCNQ3 K+ Current Amplitudes by Controlling Channel Trafficking |
Q36548403 | The Sensorless Pore Module of Voltage-gated K+ Channel Family 7 Embodies the Target Site for the Anticonvulsant Retigabine |
Q41879401 | The Voltage-Sensing Domain of K(v)7.2 Channels as a Molecular Target for Epilepsy-Causing Mutations and Anticonvulsants. |
Q28472214 | The acrylamide (S)-2 as a positive and negative modulator of Kv7 channels expressed in Xenopus laevis oocytes |
Q48810175 | Three mechanisms underlie KCNQ2/3 heteromeric potassium M-channel potentiation. |
Q39194934 | Voltage dependence of the Ca(2+)-activated K(+) channel K(Ca)3.1 in human erythroleukemia cells. |
Q40145551 | Zinc pyrithione-mediated activation of voltage-gated KCNQ potassium channels rescues epileptogenic mutants |
Q48221664 | β-Secretase BACE1 regulates hippocampal and reconstituted M-currents in a β-subunit-like fashion. |
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