Roles of alternative splicing in the functional properties of inner ear-specific KCNQ4 channels. - Wikidata - awgldk - TriplyDB

Roles of alternative splicing in the functional properties of inner ear-specific KCNQ4 channels.

Roles of alternative splicing in the functional properties of inner ear-specific KCNQ4 channels.

http://www.wikidata.org/entity/Q46398878

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Cellular mechanisms of mutations in Kv7.1: auditory functions in Jervell and Lange-Nielsen syndrome vs. Romano-Ward syndrome The candidate splicing factor Sfswap regulates growth and patterning of inner ear sensory organs Structure of a Ca2+/CaM:Kv7.4 (KCNQ4) B-Helix Complex Provides Insight into M Current Modulation The voltage-gated potassium channel subfamily KQT member 4 (KCNQ4) displays parallel evolution in echolocating bats.Malleable ribonucleoprotein machine: protein intrinsic disorder in the Saccharomyces cerevisiae spliceosome.KCNQ5 channels control resting properties and release probability of a synapse Cellular and molecular mechanisms of autosomal dominant form of progressive hearing loss, DFNA2.Effect of salicylate on KCNQ4 of the guinea pig outer hair cell.Alternative splicing of Na(V)1.7 exon 5 increases the impact of the painful PEPD mutant channel I1461T.Kv7-type channel currents in spiral ganglion neurons: involvement in sensorineural hearing loss.KCNQ5/K(v)7.5 potassium channel expression and subcellular localization in primate retinal pigment epithelium and neural retina Postnatal expression of an apamin-sensitive k(ca) current in vestibular calyx terminals Molecular microdomains in a sensory terminal, the vestibular calyx ending Mechanisms of Calmodulin Regulation of Different Isoforms of Kv7.4 K+ Channels Impaired surface expression and conductance of the KCNQ4 channel lead to sensorineural hearing loss KCNQ4 mutations associated with nonsyndromic progressive sensorineural hearing loss Differential Regulation of PI(4,5)P2 Sensitivity of Kv7.2 and Kv7.3 Channels by Calmodulin.Effect of capsaicin on potassium conductance and electromotility of the guinea pig outer hair cell.KCNQ modulators reveal a key role for KCNQ potassium channels in regulating the tone of rat pulmonary artery smooth muscle.Coordinated Expression of Two Types of Low-Threshold K+ Channels Establishes Unique Single Spiking of Mauthner Cells among Segmentally Homologous Neurons in the Zebrafish Hindbrain.Dorsoventral differences in Kv7/M-current and its impact on resonance, temporal summation and excitability in rat hippocampal pyramidal cells.Intracellular Regulome Variability Along the Organ of Corti: Evidence, Approaches, Challenges, and Perspective.

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P2860

Roles of alternative splicing in the functional properties of inner ear-specific KCNQ4 channels.

http://www.wikidata.org/entity/Q46398878

description

2007 nî lūn-bûn

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2007年の論文

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2007年学术文章

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2007年学术文章

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2007年学术文章

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2007年学术文章

@zh-hans

2007年学术文章

@zh-my

2007年学术文章

@zh-sg

2007年學術文章

@yue

2007年學術文章

@zh-hant

name

Roles of alternative splicing ...... r ear-specific KCNQ4 channels.

@en

Roles of alternative splicing ...... r ear-specific KCNQ4 channels.

@nl

type

label

Roles of alternative splicing ...... r ear-specific KCNQ4 channels.

@en

Roles of alternative splicing ...... r ear-specific KCNQ4 channels.

@nl

prefLabel

Roles of alternative splicing ...... r ear-specific KCNQ4 channels.

@en

Roles of alternative splicing ...... r ear-specific KCNQ4 channels.

@nl

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Journal of Biological Chemistry

P1476

Roles of alternative splicing ...... r ear-specific KCNQ4 channels.

@en

P2093

Ana E Vazquez

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Bechara Kachar

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Dongguang Wei

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Evgueni Petrov

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Jiling Mo

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Kirk W Beisel

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Lilian E Calisto

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Liping Nie

http://www.w3.org/2001/XMLSchema#string

Tonghui Xu

http://www.w3.org/2001/XMLSchema#string

Weihong Feng

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P2860

KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafness

Molecular cloning and functional expression of KCNQ5, a potassium channel subunit that may contribute to neuronal M-current diversity

A mechanistic link between an inherited and an acquired cardiac arrhythmia: HERG encodes the IKr potassium channel

A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome

A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns

A potassium channel mutation in neonatal human epilepsy

Polarized axonal surface expression of neuronal KCNQ channels is mediated by multiple signals in the KCNQ2 and KCNQ3 C-terminal domains

Myokymia and neonatal epilepsy caused by a mutation in the voltage sensor of the KCNQ2 K+ channel

The identification and characterization of a noncontinuous calmodulin-binding site in noninactivating voltage-dependent KCNQ potassium channels

Determination of the subunit stoichiometry of a voltage-activated potassium channel

P304

23899-23909

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scholarly article

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10.1074/JBC.M702108200

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P433

33

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P478

282

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Ebenezer N. Yamoah

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2007-06-07T00:00:00Z

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6276462

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17561493

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