(Q42645829)

4 November 2017

title

Reduced voltage dependence of inactivation in the SCN5A sodium channel mutation delF1617. (English)

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4 November 2017

Tiehua Chen

1

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4 November 2017

Masashi Inoue

series ordinal

2

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4 November 2017

Michael F Sheets

series ordinal

3

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4 November 2017

language of work or name

1 reference

21 January 2005

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American Journal of Physiology Heart and Circulatory Physiology

4 November 2017

published in

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4 November 2017

volume

288

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4 November 2017

issue

6

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4 November 2017

page(s)

H2666-76

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Brugada syndrome: 1992-2002: a historical perspective

4 November 2017

cites work

1 reference

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SCN5A mutation (T1620M) causing Brugada syndrome exhibits different phenotypes when expressed in Xenopus oocytes and mammalian cells

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Sodium channel mutations in paramyotonia congenita uncouple inactivation from activation

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Ionic mechanisms responsible for the electrocardiographic phenotype of the Brugada syndrome are temperature dependent

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Effects of III-IV linker mutations on human heart Na+ channel inactivation gating

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21 January 2018

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Phenotypic characterization of a novel long-QT syndrome mutation (R1623Q) in the cardiac sodium channel.

21 January 2018

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21 January 2018

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21 January 2018

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Movement of voltage sensor S4 in domain 4 is tightly coupled to sodium channel fast inactivation and gating charge immobilization

21 January 2018

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A ubiquitous splice variant and a common polymorphism affect heterologous expression of recombinant human SCN5A heart sodium channels

21 January 2018

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A de novo missense mutation of human cardiac Na+ channel exhibiting novel molecular mechanisms of long QT syndrome.

21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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The Na channel voltage sensor associated with inactivation is localized to the external charged residues of domain IV, S4.

21 January 2018

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Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2

21 January 2018

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21 January 2018

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Myasthenic syndrome caused by mutation of the SCN4A sodium channel

21 January 2018

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Functional suppression of sodium channels by beta(1)-subunits as a molecular mechanism of idiopathic ventricular fibrillation

21 January 2018

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Enhanced Na(+) channel intermediate inactivation in Brugada syndrome

21 January 2018

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21 January 2018

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Congenital long-QT syndrome caused by a novel mutation in a conserved acidic domain of the cardiac Na+ channel.

21 January 2018

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Molecular basis of charge movement in voltage-gated sodium channels

21 January 2018

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10.1152/AJPHEART.00521.2004

21 January 2018

Identifiers

DOI

1 reference

4 November 2017

1 reference