Regions responsible for the assembly of inwardly rectifying potassium channels.
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Mutations in potassium channel Kir2.6 cause susceptibility to thyrotoxic hypokalemic periodic paralysisHeteromerization of Kir2.x potassium channels contributes to the phenotype of Andersen's syndrome.A carboxy-terminal domain determines the subunit specificity of KCNQ K+ channel assembly.A mechanism for ATP-sensitive potassium channel diversity: Functional coassembly of two pore-forming subunitsFunctional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome)Ablation of a Ca2+-activated K+ channel (SK2 channel) results in action potential prolongation in atrial myocytes and atrial fibrillationMapping of the physical interaction between the intracellular domains of an inwardly rectifying potassium channel, Kir6.2Identification of human Kir2.2 (KCNJ12) gene encoding functional inward rectifier potassium channel in both mammalian cells and Xenopus oocytesIdentification of domains that control the heteromeric assembly of Kir5.1/Kir4.0 potassium channelsNumber and stoichiometry of subunits in the native atrial G-protein-gated K+ channel, IKAChEvidence 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+ channelProximal C-terminal domain of sulphonylurea receptor 2A interacts with pore-forming Kir6 subunits in KATP channelsThe ATP-sensitive K(+)-channel (K(ATP)) controls early left-right patterning in Xenopus and chick embryos.Cellular and molecular mechanisms of autosomal dominant form of progressive hearing loss, DFNA2.Rat homolog of sulfonylurea receptor 2B determines glibenclamide sensitivity of ROMK2 in Xenopus laevis oocyte.Molecular diversity and regulation of renal potassium channels.The metal-ion-dependent adhesion site in the Von Willebrand factor-A domain of alpha2delta subunits is key to trafficking voltage-gated Ca2+ channels.Equalizing excitation-inhibition ratios across visual cortical neuronsSynchrotron radiation circular dichroism spectroscopy-defined structure of the C-terminal domain of NaChBac and its role in channel assembly.Graded contribution of the Gbeta gamma binding domains to GIRK channel activation.Assembly of ROMK1 (Kir 1.1a) inward rectifier K+ channel subunits involves multiple interaction sitesAsymmetrical contributions of subunit pore regions to ion selectivity in an inward rectifier K+ channel.The consequences of disrupting cardiac inwardly rectifying K(+) current (I(K1)) as revealed by the targeted deletion of the murine Kir2.1 and Kir2.2 genes.Molecular dissection of the inward rectifier potassium current (IK1) in rabbit cardiomyocytes: evidence for heteromeric co-assembly of Kir2.1 and Kir2.2.GCN4 enhances the stability of the pore domain of potassium channel KcsA.Selective heteromeric assembly of cyclic nucleotide-gated channelsFunctional role of inward rectifier current in heart probed by Kir2.1 overexpression and dominant-negative suppression.The upregulation of α2δ-1 subunit modulates activity-dependent Ca2+ signals in sensory neuronsExpression of three topologically distinct membrane proteins elicits unique stress response pathways in the yeast Saccharomyces cerevisiaeLovastatin-Induced Phosphatidylinositol-4-Phosphate 5-Kinase Diffusion from Microvilli Stimulates ROMK Channels.Human myoblast fusion requires expression of functional inward rectifier Kir2.1 channelsA mutation linked with Bartter's syndrome locks Kir 1.1a (ROMK1) channels in a closed stateDominant-negative mutants identify a role for GIRK channels in D3 dopamine receptor-mediated regulation of spontaneous secretory activityStructural and functional determinants of conserved lipid interaction domains of inward rectifying Kir6.2 channelsRare KCNJ18 variants do not explain hypokalaemic periodic paralysis in 263 unrelated patients.Abnormalities of pancreatic islets by targeted expression of a dominant-negative KATP channel.Functional and clinical characterization of a mutation in KCNJ2 associated with Andersen-Tawil syndromeThe stargazin-related protein gamma 7 interacts with the mRNA-binding protein heterogeneous nuclear ribonucleoprotein A2 and regulates the stability of specific mRNAs, including CaV2.2.KCNJ2 mutation results in Andersen syndrome with sex-specific cardiac and skeletal muscle phenotypes.ESCRT regulates surface expression of the Kir2.1 potassium channel.
P2860
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P2860
Regions responsible for the assembly of inwardly rectifying potassium channels.
description
1996 nî lūn-bûn
@nan
1996年の論文
@ja
1996年論文
@yue
1996年論文
@zh-hant
1996年論文
@zh-hk
1996年論文
@zh-mo
1996年論文
@zh-tw
1996年论文
@wuu
1996年论文
@zh
1996年论文
@zh-cn
name
Regions responsible for the assembly of inwardly rectifying potassium channels.
@en
type
label
Regions responsible for the assembly of inwardly rectifying potassium channels.
@en
prefLabel
Regions responsible for the assembly of inwardly rectifying potassium channels.
@en
P2093
P1433
P1476
Regions responsible for the assembly of inwardly rectifying potassium channels.
@en
P2093
P304
P356
10.1016/S0092-8674(00)81993-5
P407
P577
1996-11-01T00:00:00Z