Obligatory heterotetramerization of three previously uncharacterized Kv channel alpha-subunits identified in the human genome.
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Mutation of histidine 105 in the T1 domain of the potassium channel Kv2.1 disrupts heteromerization with Kv6.3 and Kv6.4Fluorescence measurements reveal stoichiometry of K+ channels formed by modulatory and delayed rectifier alpha-subunits.Domain analysis of Kv6.3, an electrically silent channelMutations in the gene KCNV2 encoding a voltage-gated potassium channel subunit cause "cone dystrophy with supernormal rod electroretinogram" in humansKv5, Kv6, Kv8, and Kv9 subunits: No simple silent bystandersA novel mechanism for the suppression of a voltage-gated potassium channel by glucose-dependent insulinotropic polypeptide: protein kinase A-dependent endocytosis.Convergent evolution of marine mammals is associated with distinct substitutions in common genesIndependent movement of the voltage sensors in KV2.1/KV6.4 heterotetramersLocalization and targeting of voltage-dependent ion channels in mammalian central neurons.Voltage-gated potassium channel KCNV2 (Kv8.2) contributes to epilepsy susceptibility.Biochemical characterization of the native Kv2.1 potassium channel.Studies of alpha-helicity and intersegmental interactions in voltage-gated Na+ channels: S2D4.Conserved negative charges in the N-terminal tetramerization domain mediate efficient assembly of Kv2.1 and Kv2.1/Kv6.4 channels.Fine mapping of an epilepsy modifier gene on mouse Chromosome 19.Gestational high-fat diet and bisphenol A exposure heightens mammary cancer risk.Expression and distribution of voltage-gated ion channels in ferret sinoatrial nodeThe electrically silent Kv6.4 subunit confers hyperpolarized gating charge movement in Kv2.1/Kv6.4 heterotetrameric channels.Auxiliary KCNE subunits modulate both homotetrameric Kv2.1 and heterotetrameric Kv2.1/Kv6.4 channels.Phenotypic characteristics including in vivo cone photoreceptor mosaic in KCNV2-related "cone dystrophy with supernormal rod electroretinogram"Expanded functional diversity of shaker K(+) channels in cnidarians is driven by gene expansion.Novel mutations in the KCNV2 gene in patients with cone dystrophy and a supernormal rod electroretinogram.Major diversification of voltage-gated K+ channels occurred in ancestral parahoxozoans.The subfamily-specific interaction between Kv2.1 and Kv6.4 subunits is determined by interactions between the N- and C-termini.Contribution of Kv2.1 channels to the delayed rectifier current in freshly dispersed smooth muscle cells from rabbit urethra.Modulation of Closed-State Inactivation in Kv2.1/Kv6.4 Heterotetramers as Mechanism for 4-AP Induced Potentiation.KV2.1 and electrically silent KV channel subunits control excitability and contractility of guinea pig detrusor smooth muscleFRET imaging in living maize cells reveals that plasma membrane aquaporins interact to regulate their subcellular localization.KCNE Regulation of K(+) Channel Trafficking - a Sisyphean Task?Myogenic regulation of arterial diameter: role of potassium channels with a focus on delayed rectifier potassium current.Dual-targeting of Arabidopsis DMP1 isoforms to the tonoplast and the plasma membraneModeling-independent elucidation of inactivation pathways in recombinant and native A-type Kv channels.Functional analysis of missense mutations in Kv8.2 causing cone dystrophy with supernormal rod electroretinogram.KV1 and KV3 Potassium Channels Identified at Presynaptic Terminals of the Corticostriatal Synapses in Rat.Surface expression and distribution of voltage-gated potassium channels in neurons (Review).Voltage-gated potassium channels as therapeutic targets.Pharmacological modulation of voltage-gated potassium channels as a therapeutic strategy.Electrically silent Kv subunits: their molecular and functional characteristics.K(+) channels: function-structural overview.Potassium channels in pancreatic duct epithelial cells: their role, function and pathophysiological relevance.A novel mutation (T65P) in the PAS domain of the human potassium channel HERG results in the long QT syndrome by trafficking deficiency.
P2860
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P2860
Obligatory heterotetramerization of three previously uncharacterized Kv channel alpha-subunits identified in the human genome.
description
2002 nî lūn-bûn
@nan
2002 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
Obligatory heterotetramerizati ...... identified in the human genome
@nl
Obligatory heterotetramerizati ...... dentified in the human genome.
@ast
Obligatory heterotetramerizati ...... dentified in the human genome.
@en
Obligatory heterotetramerizati ...... dentified in the human genome.
@en-gb
type
label
Obligatory heterotetramerizati ...... identified in the human genome
@nl
Obligatory heterotetramerizati ...... dentified in the human genome.
@ast
Obligatory heterotetramerizati ...... dentified in the human genome.
@en
Obligatory heterotetramerizati ...... dentified in the human genome.
@en-gb
prefLabel
Obligatory heterotetramerizati ...... identified in the human genome
@nl
Obligatory heterotetramerizati ...... dentified in the human genome.
@ast
Obligatory heterotetramerizati ...... dentified in the human genome.
@en
Obligatory heterotetramerizati ...... dentified in the human genome.
@en-gb
P2093
P2860
P3181
P356
P1476
Obligatory heterotetramerizati ...... identified in the human genome
@en
P2093
D Van Hoorick
N Ottschytsch
P2860
P304
P3181
P356
10.1073/PNAS.122617999
P407
P577
2002-06-01T00:00:00Z