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

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14 March 2018

author name string

Nora Rozengurt

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14 March 2018

Chi-Sung Chiu

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14 March 2018

Henry A Lester

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14 March 2018

Clemens Neusch

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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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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.

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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

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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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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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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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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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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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7 January 2021

The molecular basis of long QT syndrome and prospects for therapy

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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

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14 March 2018