alpha-1-syntrophin mutation and the long-QT syndrome: a disease of sodium channel disruption (Q24651586)

10

object named as

Michael J Ackerman

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author name string

Geru Wu

1

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Tomohiko Ai

2

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Jeffrey J Kim

3

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Bhagyalaxmi Mohapatra

4

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Yutao Xi

5

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Zhaohui Li

6

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Shahrzad Abbasi

7

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Enkhsaikhan Purevjav

8

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Kaveh Samani

9

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Ming Qi

11

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Arthur J Moss

12

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Wataru Shimizu

13

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Jie Cheng

15

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Matteo Vatta

Circulation: Arrhythmia and Electrophysiology

16

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language of work or name

English

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publication date

August 2008

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published in

1 reference

Mutation of an A-kinase-anchoring protein causes long-QT syndrome

volume

1

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issue

3

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page(s)

193-201

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cites work

1 reference

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Novel mechanism for sudden infant death syndrome: persistent late sodium current secondary to mutations in caveolin-3

7 April 2017

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Mutant caveolin-3 induces persistent late sodium current and is associated with long-QT syndrome

7 April 2017

1 reference

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Ankyrin-B mutation causes type 4 long-QT cardiac arrhythmia and sudden cardiac death

7 April 2017

1 reference

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Gamma1- and gamma2-syntrophins, two novel dystrophin-binding proteins localized in neuronal cells

7 April 2017

1 reference

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Cloning of human basic A1, a distinct 59-kDa dystrophin-associated protein encoded on chromosome 8q23-24

7 April 2017

1 reference

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Heterogeneity of the 59-kDa dystrophin-associated protein revealed by cDNA cloning and expression

7 April 2017

1 reference

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Interaction of muscle and brain sodium channels with multiple members of the syntrophin family of dystrophin-associated proteins

7 April 2017

1 reference

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Mouse α1- and β2-Syntrophin Gene Structure, Chromosome Localization, and Homology with a Discs Large Domain

7 April 2017

1 reference

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Molecular aspects of the congenital and acquired Long QT Syndrome: clinical implications

7 April 2017

1 reference

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Common NOS1AP variants are associated with a prolonged QTc interval in the Rotterdam Study

28 September 2017

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Management of long QT syndrome

28 September 2017

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Molecular basis of arrhythmias

28 September 2017

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Molecular etiopathogenesis of limb girdle muscular and congenital muscular dystrophies: boundaries and contiguities

28 September 2017

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A novel mutation L619F in the cardiac Na+ channel SCN5A associated with long-QT syndrome (LQT3): a role for the I-II linker in inactivation gating

28 September 2017

1 reference

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Syntrophin gamma 2 regulates SCN5A gating by a PDZ domain-mediated interaction

28 September 2017

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Cardiac arrhythmias: the genetic connection

28 September 2017

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

28 September 2017

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Diagnostic criteria for the long QT syndrome. An update

28 September 2017

1 reference

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A common SCN5A variant alters the responsiveness of human sodium channels to class I antiarrhythmic agents

28 September 2017

1 reference

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Improved splice site detection in Genie

30 May 2018

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Cardiac sodium channel Nav1.5 is regulated by a multiprotein complex composed of syntrophins and dystrophin.

30 May 2018

1 reference

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Two forms of mouse syntrophin, a 58 kd dystrophin-associated protein, differ in primary structure and tissue distribution

28 November 2018

1 reference

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ECG T-Wave Patterns in Genetically Distinct Forms of the Hereditary Long QT Syndrome

28 November 2018

1 reference

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