(Q50723364)

18 March 2018

title

Characterization of S818L mutation in HERG C-terminus in LQT2. Modification of activation-deactivation gating properties. (English)

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18 March 2018

author

Toshihiro Tanaka

8

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18 March 2018

author name string

T Nakajima

1

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18 March 2018

M Kurabayashi

2

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18 March 2018

Y Ohyama

3

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18 March 2018

Y Kaneko

4

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18 March 2018

T Furukawa

5

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18 March 2018

T Itoh

6

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18 March 2018

Y Taniguchi

7

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18 March 2018

Y Nakamura

9

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18 March 2018

M Hiraoka

10

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18 March 2018

R Nagai

11

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18 March 2018

language of work or name

English

0 references

publication date

1 September 2000

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18 March 2018

published in

FEBS Letters

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18 March 2018

volume

481

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18 March 2018

issue

2

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18 March 2018

page(s)

197-203

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18 March 2018

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

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901988-8

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901988-8

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%2800%2901988-8

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%2800%2901988-8

A family of potassium channel genes related to eag in Drosophila and mammals

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901988-8

Two components of cardiac delayed rectifier K+ current. Differential sensitivity to block by class III antiarrhythmic agents

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901988-8

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/10.1016%2FS0014-5793%2800%2901988-8

Missense mutation in the pore region of HERG causes familial long QT syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901988-8

A mutation in HERG associated with notched T waves in long QT syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901988-8

Four novel KVLQT1 and four novel HERG mutations in familial long-QT syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901988-8

Genomic organization and mutational analysis of HERG, a gene responsible for familial long QT syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901988-8

Spectrum of HERG K+-channel dysfunction in an inherited cardiac arrhythmia

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901988-8

Novel mechanism of HERG current suppression in LQT2: shift in voltage dependence of HERG inactivation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901988-8

Voltage-shift of the current activation in HERG S4 mutation (R534C) in LQT2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901988-8

HERG channel dysfunction in human long QT syndrome. Intracellular transport and functional defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901988-8

Novel mechanism associated with an inherited cardiac arrhythmia: defective protein trafficking by the mutant HERG (G601S) potassium channel.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901988-8

Long QT syndrome-associated mutations in the Per-Arnt-Sim (PAS) domain of HERG potassium channels accelerate channel deactivation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901988-8

Novel gain-of-function mechanism in K(+) channel-related long-QT syndrome: altered gating and selectivity in the HERG1 N629D mutant.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901988-8

The human delta1261 mutation of the HERG potassium channel results in a truncated protein that contains a subunit interaction domain and decreases the channel expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901988-8

The inward rectification mechanism of the HERG cardiac potassium channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901988-8

A quantitative analysis of the activation and inactivation kinetics of HERG expressed in Xenopus oocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901988-8

A K+ channel splice variant common in human heart lacks a C-terminal domain required for expression of rapidly activating delayed rectifier current

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901988-8

The dominant negative LQT2 mutation A561V reduces wild-type HERG expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901988-8

C-terminal HERG mutations: the role of hypokalemia and a KCNQ1-associated mutation in cardiac event occurrence

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901988-8

Gated access to the pore of a voltage-dependent K+ channel

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901988-8

10.1016/S0014-5793(00)01988-8

7 January 2021

Identifiers

DOI

1 reference

18 March 2018

1 reference

18 March 2018