KCNQ1/KCNE1 potassium channels in mammalian vestibular dark cells
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KCNE1 and KCNE3 beta-subunits regulate membrane surface expression of Kv12.2 K(+) channels in vitro and form a tripartite complex in vivoIon channel gene expression in the inner earPolymorphisms in KCNE1 or KCNE3 are not associated with Ménière disease in the Caucasian populationKCNQ1/KCNE1 channels during germ-cell differentiation in the rat: expression associated with testis pathologiesHomomeric and heteromeric assembly of KCNQ (Kv7) K+ channels assayed by total internal reflection fluorescence/fluorescence resonance energy transfer and patch clamp analysis.A quantitative survey of gravity receptor function in mutant mouse strains.Identification of a protein-protein interaction between KCNE1 and the activation gate machinery of KCNQ1The KCNQ1 potassium channel: from gene to physiological function.The multifaceted phenotype of the knockout mouse for the KCNE1 potassium channel gene.Identification of a key residue in Kv7.1 potassium channel essential for sensing external potassium ions.Protein kinase A stimulates Kv7.1 surface expression by regulating Nedd4-2-dependent endocytic trafficking.KCNQ1 and KCNE1 K+ channel components are involved in early left-right patterning in Xenopus laevis embryos.Hypothyroidism of gene-targeted mice lacking Kcnq1.Voltage-dependent C-type inactivation in a constitutively open K+ channelStria vascularis and vestibular dark cells: characterisation of main structures responsible for inner-ear homeostasis, and their pathophysiological relations.Enhanced insulin sensitivity of gene-targeted mice lacking functional KCNQ1The KCNE Tango - How KCNE1 Interacts with Kv7.1.Functional IsK/KvLQT1 potassium channel in a new corticosteroid-sensitive cell line derived from the inner ear.Variants in the KCNE1 or KCNE3 gene and risk of Ménière's disease: A meta-analysis.Trafficking of the IKs -complex in MDCK cells: site of subunit assembly and determinants of polarized localization.Contribution of KCNQ1 to the regulatory volume decrease in the human mammary epithelial cell line MCF-7.Modulation of ERG channels by XE991.KCNE1 subunits require co-assembly with K+ channels for efficient trafficking and cell surface expression.Vestibular dysfunction is a clinical feature of the Jervell and Lange-Nielsen Syndrome.Upregulation of KCNQ1/KCNE1 K+ channels by Klotho.An allosteric gating model recapitulates the biophysical properties of IK,L expressed in mouse vestibular type I hair cells.Inhibition of the heterotetrameric K+ channel KCNQ1/KCNE1 by the AMP-activated protein kinase.Deafness in LIMP2-deficient mice due to early loss of the potassium channel KCNQ1/KCNE1 in marginal cells of the stria vascularis.Ion channel proteins in mouse and human vestibular tissue.An arrhythmia susceptibility gene in Caenorhabditis elegans.Regulation and physiological function of Nav1.5 and KCNQ1 channelsA novel cancer syndrome caused by -deficiency in the golden Syrian hamster
P2860
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P2860
KCNQ1/KCNE1 potassium channels in mammalian vestibular dark cells
description
2001 nî lūn-bûn
@nan
2001 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի մարտին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
KCNQ1/KCNE1 potassium channels in mammalian vestibular dark cells
@ast
KCNQ1/KCNE1 potassium channels in mammalian vestibular dark cells
@en
KCNQ1/KCNE1 potassium channels in mammalian vestibular dark cells
@nl
type
label
KCNQ1/KCNE1 potassium channels in mammalian vestibular dark cells
@ast
KCNQ1/KCNE1 potassium channels in mammalian vestibular dark cells
@en
KCNQ1/KCNE1 potassium channels in mammalian vestibular dark cells
@nl
prefLabel
KCNQ1/KCNE1 potassium channels in mammalian vestibular dark cells
@ast
KCNQ1/KCNE1 potassium channels in mammalian vestibular dark cells
@en
KCNQ1/KCNE1 potassium channels in mammalian vestibular dark cells
@nl
P2093
P1433
P1476
KCNQ1/KCNE1 potassium channels in mammalian vestibular dark cells
@en
P2093
J Barhanin
S Kupershmidt
P304
P356
10.1016/S0378-5955(00)00268-9
P407
P577
2001-03-01T00:00:00Z