Functional effects of mutations in KvLQT1 that cause long QT syndrome. (Q48914938)

16 February 2018

title

Functional effects of mutations in KvLQT1 that cause long QT syndrome. (English)

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16 February 2018

author name string

Wang Z

1

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16 February 2018

Tristani-Firouzi M

2

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16 February 2018

Xu Q

3

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16 February 2018

Lin M

4

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16 February 2018

Keating MT

5

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16 February 2018

Sanguinetti MC

6

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16 February 2018

publication date

1 June 1999

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16 February 2018

Journal of Cardiovascular Electrophysiology

published in

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volume

10

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16 February 2018

issue

6

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16 February 2018

page(s)

817-826

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16 February 2018

SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1999.TB00262.X

A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1999.TB00262.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1999.TB00262.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1999.TB00262.X

Molecular basis of the long-QT syndrome associated with deafness.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1999.TB00262.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1999.TB00262.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1999.TB00262.X

Dominant-negative KvLQT1 mutations underlie the LQT1 form of long QT syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1999.TB00262.X

Properties of KvLQT1 K+ channel mutations in Romano-Ward and Jervell and Lange-Nielsen inherited cardiac arrhythmias

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1999.TB00262.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1999.TB00262.X

KvLQT1, a voltage-gated potassium channel responsible for human cardiac arrhythmias

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1999.TB00262.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1999.TB00262.X

Site-specific mutations in a minimal voltage-dependent K+ channel alter ion selectivity and open-channel block

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1999.TB00262.X

Inhibition of IKs in guinea pig cardiac myocytes and guinea pig IsK channels by the chromanol 293B.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1999.TB00262.X

IsK and KvLQT1: mutation in either of the two subunits of the slow component of the delayed rectifier potassium channel can cause Jervell and Lange-Nielsen syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1999.TB00262.X

Mutation of the gene for IsK associated with both Jervell and Lange-Nielsen and Romano-Ward forms of Long-QT syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1999.TB00262.X

Suppression of slow delayed rectifier current by a truncated isoform of KvLQT1 cloned from normal human heart

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1999.TB00262.X

Influence of the genotype on the clinical course of the long-QT syndrome. International Long-QT Syndrome Registry Research Group.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1999.TB00262.X

Multiple mechanisms in the long-QT syndrome. Current knowledge, gaps, and future directions. The SADS Foundation Task Force on LQTS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1999.TB00262.X

The S4-S5 loop contributes to the ion-selective pore of potassium channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1999.TB00262.X

Putative receptor for the cytoplasmic inactivation gate in the Shaker K+ channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1999.TB00262.X

10.1111/J.1540-8167.1999.TB00262.X

21 January 2018

Identifiers

DOI

1 reference

16 February 2018

PubMed ID

10376919

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16 February 2018