Clustering and enhanced activity of an inwardly rectifying potassium channel, Kir4.1, by an anchoring protein, PSD-95/SAP90
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The cloning, genomic organization and tissue expression profile of the human DLG5 geneThe multivalent PDZ domain-containing protein PDZK1 regulates transport activity of renal urate-anion exchanger URAT1 via its C terminusDifferent isoforms of synapse-associated protein, SAP97, are expressed in the heart and have distinct effects on the voltage-gated K+ channel Kv1.5PSD-95 promotes Fyn-mediated tyrosine phosphorylation of the N-methyl-D-aspartate receptor subunit NR2ASpecific localization of an inwardly rectifying K(+) channel, Kir4.1, at the apical membrane of rat gastric parietal cells; its possible involvement in K(+) recycling for the H(+)-K(+)-pumpMolecular cloning and characterization of a novel splicing variant of the Kir3.2 subunit predominantly expressed in mouse testisExpression of a functional Kir4 family inward rectifier K+ channel from a gene cloned from mouse liverA sequence motif responsible for ER export and surface expression of Kir2.0 inward rectifier K(+) channelsN-terminal PDZ-binding domain in Kv1 potassium channelsFunctional Kir7.1 channels localized at the root of apical processes in rat retinal pigment epitheliumEvidence for direct physical association between a K+ channel (Kir6.2) and an ATP-binding cassette protein (SUR1) which affects cellular distribution and kinetic behavior of an ATP-sensitive K+ channelElasticity and adhesion force mapping reveals real-time clustering of growth factor receptors and associated changes in local cellular rheological propertiesA hyperprostaglandin E syndrome mutation in Kir1.1 (renal outer medullary potassium) channels reveals a crucial residue for channel function in Kir1.3 channels.A novel junction-like membrane complex in the optic nerve astrocyte of the Japanese macaque with a possible relation to a potassium ion channel.Downregulation of gene expression in the ageing lens: a possible contributory factor in senile cataract.MUPP1 complexes renal K+ channels to alter cell surface expression and whole cell currents.Signaling pathways are focused at specialized regions of the plasma membrane by scaffolding proteins of the MAGUK family.Shear stress regulates the endothelial Kir2.1 ion channel.Potassium buffering in the central nervous systemMolecular aspects of structure, gating, and physiology of pH-sensitive background K2P and Kir K+-transport channels.Human slack potassium channel mutations increase positive cooperativity between individual channelsCell signal control of the G protein-gated potassium channel and its subcellular localization.PSD-95 and SAP97 exhibit distinct mechanisms for regulating K(+) channel surface expression and clustering.Tandem gramicidin channels cross-linked by streptavidin.Distinct structural requirements for clustering and immobilization of K+ channels by PSD-95.SAP97 regulates Kir2.3 channels by multiple mechanisms.Expression of Kir4.1 and Kir5.1 inwardly rectifying potassium channels in oligodendrocytes, the myelinating cells of the CNS.Variable loss of Kir4.1 channel function in SeSAME syndrome mutations.Lin-7 targets the Kir 2.3 channel on the basolateral membrane via a L27 domain interaction with CASK.Targeted Gene Resequencing (Astrochip) to Explore the Tripartite Synapse in Autism-Epilepsy Phenotype with Macrocephaly.Allosteric regulation and spatial distribution of kainate receptors bound to ancillary proteins.PSD-95 assembles a ternary complex with the N-methyl-D-aspartic acid receptor and a bivalent neuronal NO synthase PDZ domain.Emerging roles of Dlg-like PDZ proteins in the organization of the NMDA-type glutamatergic synapseImmunogold evidence suggests that coupling of K+ siphoning and water transport in rat retinal Müller cells is mediated by a coenrichment of Kir4.1 and AQP4 in specific membrane domains.KCNJ10 (Kir4.1) potassium channel knockout abolishes endocochlear potential.Distribution of members of the PSD-95 family of MAGUK proteins at the synaptic region of inner and outer hair cells of the guinea pig cochlea.Electrophysiological properties of rat retinal Müller (glial) cells in postnatally developing and in pathologically altered retinae.The potassium channel Kir4.1 associates with the dystrophin-glycoprotein complex via alpha-syntrophin in glia.Altered membrane physiology in Müller glial cells after transient ischemia of the rat retina.Identification of an inward rectifier potassium channel gene expressed in mouse cortical astrocytes.
P2860
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P2860
Clustering and enhanced activity of an inwardly rectifying potassium channel, Kir4.1, by an anchoring protein, PSD-95/SAP90
description
1997 nî lūn-bûn
@nan
1997 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
1997 թվականի մայիսին հրատարակված գիտական հոդված
@hy
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
name
Clustering and enhanced activi ...... nchoring protein, PSD-95/SAP90
@ast
Clustering and enhanced activi ...... nchoring protein, PSD-95/SAP90
@en
Clustering and enhanced activi ...... nchoring protein, PSD-95/SAP90
@nl
type
label
Clustering and enhanced activi ...... nchoring protein, PSD-95/SAP90
@ast
Clustering and enhanced activi ...... nchoring protein, PSD-95/SAP90
@en
Clustering and enhanced activi ...... nchoring protein, PSD-95/SAP90
@nl
prefLabel
Clustering and enhanced activi ...... nchoring protein, PSD-95/SAP90
@ast
Clustering and enhanced activi ...... nchoring protein, PSD-95/SAP90
@en
Clustering and enhanced activi ...... nchoring protein, PSD-95/SAP90
@nl
P2093
P2860
P356
P1476
Clustering and enhanced activi ...... nchoring protein, PSD-95/SAP90
@en
P2093
P2860
P304
P356
10.1074/JBC.272.20.12885
P407
P577
1997-05-16T00:00:00Z