(Q50484599)

14 March 2018

title

Time course of inner ear degeneration and deafness in mice lacking the Kir4.1 potassium channel subunit. (English)

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14 March 2018

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14 March 2018

Paulo Kofuji

4

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14 March 2018

author name string

Nora Rozengurt

1

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14 March 2018

Chi-Sung Chiu

3

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14 March 2018

Henry A Lester

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14 March 2018

Clemens Neusch

6

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14 March 2018

publication date

1 March 2003

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14 March 2018

published in

Hearing Research

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14 March 2018

volume

177

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14 March 2018

issue

1-2

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14 March 2018

page(s)

71-80

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14 March 2018

Immunological identification of an inward rectifier K+ channel (Kir4.1) in the intermediate cell (melanocyte) of the cochlear stria vascularis of gerbils and rats

cites work

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https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900799-2

7 January 2021

Homozygous deletion in KVLQT1 associated with Jervell and Lange-Nielsen syndrome.

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https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900799-2

7 January 2021

Novel mutations in KvLQT1 that affect Iks activation through interactions with Isk

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https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900799-2

7 January 2021

An ATP-dependent inwardly rectifying potassium channel, KAB-2 (Kir4. 1), in cochlear stria vascularis of inner ear: its specific subcellular localization and correlation with the formation of endocochlear potential.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900799-2

7 January 2021

Expression of an inwardly rectifying K(+) channel, Kir4.1, in satellite cells of rat cochlear ganglia

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900799-2

7 January 2021

Expression and clustered distribution of an inwardly rectifying potassium channel, KAB-2/Kir4.1, on mammalian retinal Müller cell membrane: their regulation by insulin and laminin signals

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https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900799-2

7 January 2021

Inwardly rectifying potassium channels: their molecular heterogeneity and function

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900799-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900799-2

7 January 2021

Genetic inactivation of an inwardly rectifying potassium channel (Kir4.1 subunit) in mice: phenotypic impact in retina

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https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900799-2

7 January 2021

Expression and polarized distribution of an inwardly rectifying K+ channel, Kir4.1, in rat retinal pigment epithelium.

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https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900799-2

7 January 2021

Inward rectifier potassium channels. Cloning, expression and structure-function studies.

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https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900799-2

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900799-2

7 January 2021

KCNJ10 (Kir4.1) potassium channel knockout abolishes endocochlear potential

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https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900799-2

7 January 2021

Kir4.1 potassium channel subunit is crucial for oligodendrocyte development and in vivo myelination.

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7 January 2021

Inwardly rectifying potassium channels.

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7 January 2021

Molecular mechanism and functional significance of the MinK control of the KvLQT1 channel activity

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https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900799-2

7 January 2021

Autosomal recessive long-QT syndrome (Jervell Lange-Nielsen syndrome) is genetically heterogeneous

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https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900799-2

7 January 2021

Mechanism generating endocochlear potential: role played by intermediate cells in stria vascularis

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https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900799-2

7 January 2021

Three-dimensional and ultrastructural relationships between intermediate cells and capillaries in the gerbil stria vascularis

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900799-2

7 January 2021

Novel mutation in the KCNQ4 gene in a large kindred with dominant progressive hearing loss

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https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900799-2

7 January 2021

Inner ear defects induced by null mutation of the isk gene

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https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900799-2

7 January 2021

The molecular basis of long QT syndrome and prospects for therapy

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https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900799-2

7 January 2021

Pathophysiological mechanisms of dominant and recessive KVLQT1 K+ channel mutations found in inherited cardiac arrhythmias.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900799-2

7 January 2021

Modulation of kir4.1 and kir5.1 by hypercapnia and intracellular acidosis.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900799-2

7 January 2021

Biophysical and molecular mechanisms underlying the modulation of heteromeric Kir4.1-Kir5.1 channels by CO2 and pH.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900799-2

7 January 2021

10.1016/S0378-5955(02)00799-2

Identifiers

DOI

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14 March 2018

PubMed ID

12618319

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14 March 2018