(Q46398878)

21 December 2017

title

Roles of alternative splicing in the functional properties of inner ear-specific KCNQ4 channels (English)

1 reference

21 December 2017

alternative mRNA splicing, via spliceosome

main subject

1 reference

12

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author name string

Tonghui Xu

1

1 reference

21 December 2017

Liping Nie

2

1 reference

21 December 2017

Yi Zhang

3

1 reference

21 December 2017

Jiling Mo

4

1 reference

21 December 2017

Weihong Feng

5

1 reference

21 December 2017

Dongguang Wei

6

1 reference

21 December 2017

Evgueni Petrov

7

1 reference

21 December 2017

Lilian E Calisto

8

1 reference

21 December 2017

Bechara Kachar

9

1 reference

21 December 2017

Kirk W Beisel

10

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21 December 2017

Ana E Vazquez

11

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21 December 2017

language of work or name

English

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publication date

7 June 2007

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21 December 2017

Journal of Biological Chemistry

number of pages

11

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based on heuristic

inferred from page(s)

published in

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21 December 2017

volume

282

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21 December 2017

issue

33

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21 December 2017

page(s)

23899-23909

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21 December 2017

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

cites work

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702108200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702108200

KCNQ4, a K+ channel mutated in a form of dominant deafness, is expressed in the inner ear and the central auditory pathway.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702108200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702108200

Targeted disruption of the Kvlqt1 gene causes deafness and gastric hyperplasia in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702108200

Targeted point mutagenesis of mouse Kcnq1: phenotypic analysis of mice with point mutations that cause Romano-Ward syndrome in humans.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702108200

Differential expression of KCNQ4 in inner hair cells and sensory neurons is the basis of progressive high-frequency hearing loss.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702108200

Ionic currents of outer hair cells isolated from the guinea-pig cochlea

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702108200

Developmental expression of the potassium current IK,n contributes to maturation of mouse outer hair cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702108200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702108200

Calmodulin mediates Ca2+-dependent modulation of M-type K+ channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702108200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702108200

A potassium channel mutation in neonatal human epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702108200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702108200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702108200

How many conductance states do potassium channels have?

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702108200

The Nature of the Negative Resistance in Bimolecular Lipid Membranes Containing Excitability-Inducing Material

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702108200

Mechanisms of calcium channel modulation by beta-adrenergic agents and dihydropyridine calcium agonists.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702108200

The variance of sodium current fluctuations at the node of Ranvier

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702108200

A new ER trafficking signal regulates the subunit stoichiometry of plasma membrane K(ATP) channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702108200

Regulatory actions of the A-kinase anchoring protein Yotiao on a heart potassium channel downstream of PKA phosphorylation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702108200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702108200

Neuronal KCNQ potassium channels: physiology and role in disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702108200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702108200

Differential expression of outer hair cell potassium currents in the isolated cochlea of the guinea-pig

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702108200

Mice with altered KCNQ4 K+ channels implicate sensory outer hair cells in human progressive deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702108200

A PI3K pathway mediates hair cell survival and opposes gentamicin toxicity in neonatal rat organ of Corti.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702108200

Calmodulin supports both inactivation and facilitation of L-type calcium channels.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702108200

Isoform-specific modulation of voltage-gated Na(+) channels by calmodulin.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702108200

Calmodulin mediates Ca2+ sensitivity of sodium channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702108200

Novel mutations in the KCNQ2 gene link epilepsy to a dysfunction of the KCNQ2-calmodulin interaction.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702108200

Deletion of the Ca2+-activated potassium (BK) alpha-subunit but not the BKbeta1-subunit leads to progressive hearing loss

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702108200

Regulation of the voltage-gated potassium channel KCNQ4 in the auditory pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702108200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702108200

Differential K+ channel clustering activity of PSD-95 and SAP97, two related membrane-associated putative guanylate kinases

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702108200

21 January 2018

Identifiers

DOI

10.1074/JBC.M702108200

1 reference

21 December 2017

release_jiwhqzcdvvdy3mq77wiqj2lrwe

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/jiwhqzcdvvdy3mq77wiqj2lrwe

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference

21 December 2017