Identification of a heteromeric interaction that influences the rectification, gating, and pH sensitivity of Kir4.1/Kir5.1 potassium channels
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Gain-of-function defects of astrocytic Kir4.1 channels in children with autism spectrum disorders and epilepsy.Control of KirBac3.1 Potassium Channel Gating at the Interface between Cytoplasmic DomainsFunctional characterization of a prokaryotic Kir channelKir5.1 underlies long-lived subconductance levels in heteromeric Kir4.1/Kir5.1 channels from Xenopus tropicalisK(+) channelepsy: progress in the neurobiology of potassium channels and epilepsy.MUPP1 complexes renal K+ channels to alter cell surface expression and whole cell currents.Astrocyte chemoreceptors: mechanisms of H+ sensing by astrocytes in the retrotrapezoid nucleus and their possible contribution to respiratory drive.Modulation of the heteromeric Kir4.1-Kir5.1 channel by multiple neurotransmitters via Galphaq-coupled receptorsAstrocytes in the retrotrapezoid nucleus sense H+ by inhibition of a Kir4.1-Kir5.1-like current and may contribute to chemoreception by a purinergic mechanism.Subunit-subunit interactions are critical for proton sensitivity of ROMK: evidence in support of an intermolecular gating mechanismInwardly rectifying potassium channels (Kir) in central nervous system glia: a special role for Kir4.1 in glial functions.Novel KCNJ10 Gene Variations Compromise Function of Inwardly Rectifying Potassium Channel 4.1.A structural model for K2P potassium channels based on 23 pairs of interacting sites and continuum electrostatics.The salt-wasting phenotype of EAST syndrome, a disease with multifaceted symptoms linked to the KCNJ10 K+ channel.Update on the implication of potassium channels in autism: K(+) channelautism spectrum disorder.The central role of aquaporins in the pathophysiology of ischemic stroke.Destabilization of ATP-sensitive potassium channel activity by novel KCNJ11 mutations identified in congenital hyperinsulinism.Protein kinase C dependent inhibition of the heteromeric Kir4.1-Kir5.1 channelNon-equivalent role of TM2 gating hinges in heteromeric Kir4.1/Kir5.1 potassium channels.Lethal digenic mutations in the K+ channels Kir4.1 (KCNJ10) and SLACK (KCNT1) associated with severe-disabling seizures and neurodevelopmental delay.
P2860
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P2860
Identification of a heteromeric interaction that influences the rectification, gating, and pH sensitivity of Kir4.1/Kir5.1 potassium channels
description
2003 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
article publié dans la revue scientifique Journal of Biological Chemistry
@fr
artículu científicu espublizáu en 2003
@ast
im Oktober 2003 veröffentlichter wissenschaftlicher Artikel
@de
scientific article (publication date: 31 October 2003)
@en
vedecký článok (publikovaný 2003/10/31)
@sk
vědecký článek publikovaný v roce 2003
@cs
wetenschappelijk artikel (gepubliceerd op 2003/10/31)
@nl
наукова стаття, опублікована в жовтні 2003
@uk
name
Identification of a heteromeri ...... r4.1/Kir5.1 potassium channels
@ast
Identification of a heteromeri ...... r4.1/Kir5.1 potassium channels
@en
Identification of a heteromeri ...... r4.1/Kir5.1 potassium channels
@nl
type
label
Identification of a heteromeri ...... r4.1/Kir5.1 potassium channels
@ast
Identification of a heteromeri ...... r4.1/Kir5.1 potassium channels
@en
Identification of a heteromeri ...... r4.1/Kir5.1 potassium channels
@nl
prefLabel
Identification of a heteromeri ...... r4.1/Kir5.1 potassium channels
@ast
Identification of a heteromeri ...... r4.1/Kir5.1 potassium channels
@en
Identification of a heteromeri ...... r4.1/Kir5.1 potassium channels
@nl
P2093
P2860
P3181
P356
P1476
Identification of a heteromeri ...... r4.1/Kir5.1 potassium channels
@en
P2093
M Cristina D'Adamo
Maria Casamassima
Mauro Pessia
Stephen J Tucker
P2860
P304
P3181
P356
10.1074/JBC.M306596200
P407
P577
2003-10-31T00:00:00Z