A de novo missense mutation of human cardiac Na+ channel exhibiting novel molecular mechanisms of long QT syndrome. (Q48944651)

17 February 2018

title

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

1 reference

17 February 2018

author name string

Makita N

1

1 reference

17 February 2018

Shirai N

2

1 reference

17 February 2018

Nagashima M

3

1 reference

17 February 2018

Matsuoka R

4

1 reference

17 February 2018

Yamada Y

5

1 reference

17 February 2018

Tohse N

6

1 reference

17 February 2018

Kitabatake A

7

1 reference

17 February 2018

language of work or name

English

0 references

publication date

1 February 1998

1 reference

17 February 2018

published in

FEBS Letters

1 reference

17 February 2018

volume

423

1 reference

17 February 2018

page(s)

5-9

1 reference

17 February 2018

issue

1

1 reference

17 February 2018

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

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900033-7

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900033-7

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900033-7

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900033-7

Assignment of the human heart tetrodotoxin-resistant voltage-gated Na+ channel alpha-subunit gene (SCN5A) to band 3p21.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900033-7

Cardiac sodium channel mutations in patients with long QT syndrome, an inherited cardiac arrhythmia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900033-7

Molecular mechanism for an inherited cardiac arrhythmia

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900033-7

Characterization of human cardiac Na+ channel mutations in the congenital long QT syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900033-7

Pharmacological targeting of long QT mutant sodium channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900033-7

In vitro RNA synthesis with SP6 RNA polymerase

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900033-7

Voltage clamping of Xenopus laevis oocytes utilizing agarose-cushion electrodes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900033-7

On the molecular nature of the lidocaine receptor of cardiac Na+ channels. Modification of block by alterations in the alpha-subunit III-IV interdomain

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900033-7

Inactivation viewed through single sodium channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900033-7

Multiple mechanisms of Na+ channel--linked long-QT syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900033-7

Mutations in an S4 segment of the adult skeletal muscle sodium channel cause paramyotonia congenita

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900033-7

Sodium channel mutations in paramyotonia congenita uncouple inactivation from activation

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900033-7

Sodium channel mutations in paramyotonia congenita exhibit similar biophysical phenotypes in vitro

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900033-7

Structure and function of voltage-gated ion channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900033-7

Molecular basis of charge movement in voltage-gated sodium channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900033-7

Inhibition of inactivation of single sodium channels by a site-directed antibody

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900033-7

A cluster of hydrophobic amino acid residues required for fast Na(+)-channel inactivation

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900033-7

Amino acid residues required for fast Na(+)-channel inactivation: charge neutralizations and deletions in the III-IV linker

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900033-7

Gating of cardiac Na+ channels in excised membrane patches after modification by alpha-chymotrypsin

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900033-7

A reinterpretation of mammalian sodium channel gating based on single channel recording

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900033-7

Structural parts involved in activation and inactivation of the sodium channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900033-7

Multiple domains contribute to the distinct inactivation properties of human heart and skeletal muscle Na+ channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900033-7

Molecular determinants of beta 1 subunit-induced gating modulation in voltage-dependent Na+ channels.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900033-7

Structure and function of voltage-dependent sodium channels: comparison of brain II and cardiac isoforms

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2900033-7

10.1016/S0014-5793(98)00033-7

7 January 2021

Identifiers

DOI

1 reference

17 February 2018

PubMed ID

9506831

1 reference

17 February 2018