(Q38362439)

2 September 2017

title

A novel mutation (T65P) in the PAS domain of the human potassium channel HERG results in the long QT syndrome by trafficking deficiency (English)

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2 September 2017

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Aimée Paulussen

1

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2 September 2017

Adam Raes

2

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2 September 2017

Gert Matthijs

3

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2 September 2017

Dirk J Snyders

4

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2 September 2017

Nadine Cohen

5

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2 September 2017

Jeroen Aerssens

6

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2 September 2017

language of work or name

English

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publication date

26 September 2002

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Journal of Biological Chemistry

2 September 2017

number of pages

7

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based on heuristic

inferred from page(s)

published in

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2 September 2017

volume

277

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2 September 2017

issue

50

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2 September 2017

page(s)

48610-48616

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

2 September 2017

cites work

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https://api.crossref.org/works/10.1074%2FJBC.M206569200

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/10.1074%2FJBC.M206569200

HERG, a Human Inward Rectifier in the Voltage-Gated Potassium Channel Family

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M206569200

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

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Two isoforms of the mouse ether-a-go-go-related gene coassemble to form channels with properties similar to the rapidly activating component of the cardiac delayed rectifier K+ current

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206569200

Electrophysiological characterization of an alternatively processed ERG K+ channel in mouse and human hearts

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M206569200

MiRP1 forms IKr potassium channels with HERG and is associated with cardiac arrhythmia

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M206569200

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

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M206569200

Novel KCNQ1 and HERG missense mutations in Dutch long-QT families

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M206569200

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

21 January 2018

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

21 January 2018

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206569200

Long-QT syndrome-associated missense mutations in the pore helix of the HERG potassium channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206569200

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/10.1074%2FJBC.M206569200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206569200

Mutations of the S4-S5 linker alter activation properties of HERG potassium channels expressed in Xenopus oocytes

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M206569200

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

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M206569200

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/10.1074%2FJBC.M206569200

Correction of defective protein trafficking of a mutant HERG potassium channel in human long QT syndrome. Pharmacological and temperature effects

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M206569200

Retention in the endoplasmic reticulum as a mechanism of dominant-negative current suppression in human long QT syndrome

21 January 2018

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Processing of mutant cystic fibrosis transmembrane conductance regulator is temperature-sensitive

21 January 2018

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Defective aquaporin-2 trafficking in nephrogenic diabetes insipidus and correction by chemical chaperones

21 January 2018

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Crystal structure and functional analysis of the HERG potassium channel N terminus: a eukaryotic PAS domain

21 January 2018

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Genomic organization of the KCNQ1 K+ channel gene and identification of C-terminal mutations in the long-QT syndrome.

21 January 2018

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Genomic structure of three long QT syndrome genes: KVLQT1, HERG, and KCNE1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206569200

Properties of HERG channels stably expressed in HEK 293 cells studied at physiological temperature

21 January 2018

1 reference

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Obligatory heterotetramerization of three previously uncharacterized Kv channel alpha-subunits identified in the human genome.

21 January 2018

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Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patches

21 January 2018

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The binding site for channel blockers that rescue misprocessed human long QT syndrome type 2 ether-a-gogo-related gene (HERG) mutations

21 January 2018

1 reference

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Pharmacological rescue of human K(+) channel long-QT2 mutations: human ether-a-go-go-related gene rescue without block

21 January 2018

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PAS domain S-boxes in Archaea, Bacteria and sensors for oxygen and redox

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M206569200

Photoactive yellow protein: a structural prototype for the three-dimensional fold of the PAS domain superfamily.

21 January 2018

1 reference

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Fast inactivation causes rectification of the IKr channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206569200

Molecular determinants for activation and inactivation of HERG, a human inward rectifier potassium channel.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206569200

Amino terminal-dependent gating of the potassium channel rat eag is compensated by a mutation in the S4 segment

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M206569200

21 January 2018

Identifiers

DOI

10.1074/JBC.M206569200

1 reference

2 September 2017

1 reference