(Q37632853)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19913547%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

review article

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title

The rate-dependent biophysical properties of the LQT1 H258R mutant are counteracted by a dominant negative effect on channel trafficking (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19913547%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

author

Jean-Pierre Timmermans

3

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12 February 2020

Dirk J Snyders

5

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12 February 2020

author name string

Alain J Labro

1

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12 February 2020

Inge R Boulet

2

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12 February 2020

Natacha Ottschytsch

4

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12 February 2020

publication date

11 November 2009

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19913547%20AND%20SRC:MED&resulttype=core&format=json

Journal of Molecular and Cellular Cardiology

12 February 2020

published in

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19913547%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

volume

48

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12 February 2020

issue

6

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12 February 2020

page(s)

1096-1104

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19913547%20AND%20SRC:MED&resulttype=core&format=json

Long QT syndrome: novel insights into the mechanisms of cardiac arrhythmias

12 February 2020

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7 January 2021

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The S4-S5 linker directly couples voltage sensor movement to the activation gate in the human ether-a'-go-go-related gene (hERG) K+ channel.

7 January 2021

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Interactions between S4-S5 linker and S6 transmembrane domain modulate gating of HERG K+ channels

7 January 2021

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7 January 2021

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Kv channel gating requires a compatible S4-S5 linker and bottom part of S6, constrained by non-interacting residues

7 January 2021

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Long QT syndrome-associated mutations in the S4-S5 linker of KvLQT1 potassium channels modify gating and interaction with minK subunits.

7 January 2021

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Hypokalemia-induced long QT syndrome with an underlying novel missense mutation in S4-S5 linker of KCNQ1

7 January 2021

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

7 January 2021

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Rate dependency of delayed rectifier currents during the guinea-pig ventricular action potential

7 January 2021

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Autonomic control of cardiac action potentials: role of potassium channel kinetics in response to sympathetic stimulation.

7 January 2021

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Subunit interaction determines IKs participation in cardiac repolarization and repolarization reserve

7 January 2021

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Functional interactions between KCNE1 C-terminus and the KCNQ1 channel

7 January 2021

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Biophysical characteristics of a new mutation on the KCNQ1 potassium channel (L251P) causing long QT syndrome

7 January 2021

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Genomic organization and mutational analysis of KVLQT1, a gene responsible for familial long QT syndrome

7 January 2021

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Role of the S6 C-terminus in KCNQ1 channel gating

7 January 2021

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The slow component of the delayed rectifier potassium current in undiseased human ventricular myocytes

7 January 2021

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Single-channel characteristics of wild-type IKs channels and channels formed with two minK mutants that cause long QT syndrome

7 January 2021

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Single-channel properties of IKs potassium channels

7 January 2021

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Increase of the single-channel conductance of KvLQT1 potassium channels induced by the association with minK.

7 January 2021

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Location of KCNE1 relative to KCNQ1 in the I(KS) potassium channel by disulfide cross-linking of substituted cysteines

7 January 2021

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KCNQ1 and KCNE1 in the IKs channel complex make state-dependent contacts in their extracellular domains

7 January 2021

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The conduction pore of a cardiac potassium channel

7 January 2021

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A single transmembrane site in the KCNE-encoded proteins controls the specificity of KvLQT1 channel gating

7 January 2021

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Interaction of KCNE subunits with the KCNQ1 K+ channel pore

7 January 2021

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Structure of KCNE1 and Implications for How It Modulates the KCNQ1 Potassium Channel † ‡

7 January 2021

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7 January 2021

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KCNE peptides differently affect voltage sensor equilibrium and equilibration rates in KCNQ1 K+ channels

7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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Truncated KCNQ1 mutant, A178fs/105, forms hetero-multimer channel with wild-type causing a dominant-negative suppression due to trafficking defect

7 January 2021

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New KCNQ1 mutations leading to haploinsufficiency in a general population; Defective trafficking of a KvLQT1 mutant.

7 January 2021

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Functional effects of a KCNQ1 mutation associated with the long QT syndrome.

7 January 2021

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A structural requirement for processing the cardiac K+ channel KCNQ1.

7 January 2021

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The N-terminal juxtamembranous domain of KCNQ1 is critical for channel surface expression: implications in the Romano-Ward LQT1 syndrome.

7 January 2021

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The novel C-terminal KCNQ1 mutation M520R alters protein trafficking.

7 January 2021

1 reference

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10.1016/J.YJMCC.2009.10.027

7 January 2021

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19913547%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

1 reference