(Q24318498)

Potassium voltage-gated channel subfamily E regulatory subunit 1

GOA release 2020-03-11

1 reference

sensory perception of sound

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

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C Petit

10

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Pascale Guicheney

object named as

P Guicheney

12

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author name string

N Neyroud

1

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F Tesson

2

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I Denjoy

3

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M Leibovici

4

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C Donger

5

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J Barhanin

6

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S Fauré

7

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F Gary

8

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P Coumel

9

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K Schwartz

https://scigraph.springernature.com/pub.10.1038/ng0297-186

11

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language of work or name

English

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publication date

February 1997

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published in

Nature Genetics

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volume

15

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page(s)

186-9

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issue

2

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exact match

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cites work

Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval and sudden death

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-186

7 January 2021

GENETICAL ASPECTS OF THE CARDIO-AUDITORY SYNDROME OF JERVELL AND LANGE-NIELSEN (CONGENITAL DEAFNESS AND ELECTROCARDIOGRAPHIC ABNORMALITIES).

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-186

7 January 2021

The long Q-T syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-186

7 January 2021

Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-186

7 January 2021

Homozygosity mapping: a way to map human recessive traits with the DNA of inbred children

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-186

7 January 2021

Exclusion of KCNE1 (IsK) as a Candidate Gene for Jervell and Lange-Nielsen Syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-186

7 January 2021

Two long QT syndrome loci map to chromosomes 3 and 7 with evidence for further heterogeneity

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-186

7 January 2021

Genomic organization, nucleotide sequence, biophysical properties, and localization of the voltage-gated K+ channel gene KCNA4/Kv1.4 to mouse chromosome 2/human 11p14 and mapping of KCNC1/Kv3.1 to mouse 7/human 11p14.3-p15.2 and KCNA1/Kv1.1 to human

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-186

7 January 2021

Cellular localization of rat Isk protein in the stria vascularis by immunohistochemical observation

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-186

7 January 2021

An immunohistochemical and electrophysiological study on Isk protein in the stria vascularis of the guinea pig

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-186

7 January 2021

Ion transport mechanisms responsible for K+ secretion and the transepithelial voltage across marginal cells of stria vascularis in vitro

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-186

7 January 2021

Cloning of a membrane protein that induces a slow voltage-gated potassium current

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-186

7 January 2021

The protein IsK is a dual activator of K+ and Cl- channels.

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-186

7 January 2021

K(V)LQT1 and lsK (minK) proteins associate to form the I(Ks) cardiac potassium current

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-186

7 January 2021

Coassembly of K(V)LQT1 and minK (IsK) proteins to form cardiac I(Ks) potassium channel

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-186

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-186

7 January 2021

Molecular mechanism for an inherited cardiac arrhythmia

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-186

7 January 2021

How the ear's works work

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-186

7 January 2021

Overexcited or inactive: ion channels in muscle disease

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-186

7 January 2021

Osteogenesis imperfecta: translation of mutation to phenotype

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-186

7 January 2021

Genetic linkage of recessive dystrophic epidermolysis bullosa to the type VII collagen gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-186

7 January 2021

Long QT and Harvey-ras

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-186

7 January 2021

A comprehensive genetic map of the human genome based on 5,264 microsatellites

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-186

7 January 2021

Mutations in the laminin alpha 2-chain gene (LAMA2) cause merosin-deficient congenital muscular dystrophy

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-186

7 January 2021

A single protocol to detect transcripts of various types and expression levels in neural tissue and cultured cells: in situ hybridization using digoxigenin-labelled cRNA probes

1 reference

https://api.crossref.org/works/10.1038%2FNG0297-186

7 January 2021