Targeted disruption of the Kcnq1 gene produces a mouse model of Jervell and Lange-Nielsen Syndrome. (Q30497826)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11226272%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

title

Targeted disruption of the Kcnq1 gene produces a mouse model of Jervell and Lange-Nielsen Syndrome (English)

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5 November 2019

2

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Karl Pfeifer

9

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5 November 2019

author name string

M C Casimiro

1

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5 November 2019

S N Ebert

3

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J C Vary

4

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5 November 2019

A E Greene

5

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M R Franz

6

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A Grinberg

7

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S P Huang

8

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5 November 2019

language of work or name

English

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publication date

1 February 2001

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Proceedings of the National Academy of Sciences of the United States of America

5 November 2019

published in

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volume

98

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issue

5

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page(s)

2526-2531

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RARE CARDIAC ARRYTHMIAS OF THE PEDIATRIC AGE. II. SYNCOPAL ATTACKS DUE TO PAROXYSMAL VENTRICULAR FIBRILLATION. (PRESENTATION OF 1ST CASE IN ITALIAN PEDIATRIC LITERATURE)

5 November 2019

cites work

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

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20 June 2018

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

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Mutations in the gene encoding gap junction protein beta-3 associated with autosomal dominant hearing impairment

20 June 2018

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20 June 2018

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Syntenic organization of the mouse distal chromosome 7 imprinting cluster and the Beckwith-Wiedemann syndrome region in chromosome 11p15.5.

20 June 2018

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20 June 2018

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Mutations in the hminK gene cause long QT syndrome and suppress IKs function

20 June 2018

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Endothelin-1 inhibits the slow component of cardiac delayed rectifier K+ currents via a pertussis toxin-sensitive mechanism

20 June 2018

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Immunohistochemical localization of the Na-K-Cl co-transporter (NKCC1) in the gerbil inner ear.

20 June 2018

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Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

20 June 2018

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

20 June 2018

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Inner ear defects induced by null mutation of the isk gene

20 June 2018

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

20 June 2018

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

20 June 2018

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

20 June 2018

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20 June 2018

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20 June 2018

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20 June 2018

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Involvement of IsK-associated K+ channel in heart rate control of repolarization in a murine engineered model of Jervell and Lange-Nielsen syndrome.

21 January 2018

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21 January 2018

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21 January 2018

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26 November 2018

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26 November 2018

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26 November 2018

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The behavioral syndrome caused by 3,3'-iminodipropionitrile and related nitriles in the rat is associated with degeneration of the vestibular sensory hair cells

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Slowly activating voltage-dependent K+ conductance is apical pathway for K+ secretion in vestibular dark cells

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ECG T-Wave Patterns in Genetically Distinct Forms of the Hereditary Long QT Syndrome

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Identifiers

DOI

10.1073/PNAS.041398998

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5 November 2019

0 references

1 reference

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5 November 2019

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