(Q33814293)

29 July 2017

title

Mechanistic basis for LQT1 caused by S3 mutations in the KCNQ1 subunit of IKs. (English)

1 reference

29 July 2017

Amanda Degenhardt

6

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Glen F. Tibbits

object named as

Glen F Tibbits

8

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Shubhayan Sanatani

object named as

Shubhayan Sanatani

7

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CongBao Kang

object named as

Congbao Kang

4

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author name string

Jodene Eldstrom

1

1 reference

29 July 2017

Hongjian Xu

2

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29 July 2017

Daniel Werry

3

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29 July 2017

Matthew E Loewen

5

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29 July 2017

Charles Sanders

9

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29 July 2017

David Fedida

10

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29 July 2017

publication date

1 May 2010

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The Journal of General Physiology

29 July 2017

published in

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29 July 2017

volume

135

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29 July 2017

issue

5

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29 July 2017

page(s)

433-448

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describes a project that uses

29 July 2017

PyMOL

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/efetch.fcgi?db=pmc&rettype=xml&id=PMC2860592

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Common variants at ten loci influence QT interval duration in the QTGEN Study

4 July 2018

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Two separate interfaces between the voltage sensor and pore are required for the function of voltage-dependent K(+) channels

4 July 2018

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4 July 2018

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4 July 2018

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

4 July 2018

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4 July 2018

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Role of S3 and S4 transmembrane domain charged amino acids in channel biogenesis and gating of KCa2.3 and KCa3.1

4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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

21 January 2018

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Restricting excessive cardiac action potential and QT prolongation: a vital role for IKs in human ventricular muscle.

21 January 2018

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21 January 2018

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Genetic testing in the long QT syndrome: development and validation of an efficient approach to genotyping in clinical practice.

21 January 2018

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Identification of an ethnic-specific variant (V207M) of the KCNQ1 cardiac potassium channel gene in sudden unexplained death and implications from a knock-in mouse model

21 January 2018

1 reference

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Cooperative interactions between R531 and acidic residues in the voltage sensing module of hERG1 channels

21 January 2018

1 reference

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21 January 2018

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Dominant-negative KvLQT1 mutations underlie the LQT1 form of long QT syndrome

21 January 2018

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Temporal patterns of electrical remodeling in canine ventricular hypertrophy: focus on IKs downregulation and blunted beta-adrenergic activation.

21 January 2018

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A KCNQ1 V205M missense mutation causes a high rate of long QT syndrome in a First Nations community of northern British Columbia: a community-based approach to understanding the impact

21 January 2018

1 reference

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Novel mutations in KvLQT1 that affect Iks activation through interactions with Isk

21 January 2018

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12 December 2020

Ethnic differences in cardiac potassium channel variants: implications for genetic susceptibility to sudden cardiac death and genetic testing for congenital long QT syndrome

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12 December 2020

Compendium of cardiac channel mutations in 541 consecutive unrelated patients referred for long QT syndrome genetic testing

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12 December 2020

Clinical diagnosis of long QT syndrome: back to the caliper

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12 December 2020

Identifiers

DOI

10.1085/JGP.200910351

1 reference

29 July 2017

1 reference

29 July 2017

1 reference