(Q24308735)

GOA release 2020-03-11

Caveolin 3

1 reference

Sodium voltage-gated channel alpha subunit 5

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

0 references

Timothy J Kamp

11

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Jeffrey A Towbin

12

object named as

Jeffrey A Towbin

0 references

Michael J Ackerman

2

object named as

Michael J Ackerman

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author name string

Matteo Vatta

1

0 references

Bin Ye

3

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Jonathan C Makielski

4

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Enoh E Ughanze

5

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Erica W Taylor

6

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David J Tester

7

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Ravi C Balijepalli

8

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Jason D Foell

9

0 references

Zhaohui Li

Postmortem molecular analysis of SCN5A defects in sudden infant death syndrome.

10

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language of work or name

English

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publication date

14 November 2006

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published in

Circulation

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volume

114

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page(s)

2104-12

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issue

20

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cites work

1 reference

https://api.crossref.org/works/10.1161%2FCIRCULATIONAHA.106.635268

7 January 2021

Mutations in the caveolin-3 gene: When are they pathogenic?

1 reference

https://api.crossref.org/works/10.1161%2FCIRCULATIONAHA.106.635268

7 January 2021

The "final common pathway" hypothesis and inherited cardiovascular disease. The role of cytoskeletal proteins in dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1161%2FCIRCULATIONAHA.106.635268

7 January 2021

Belt-like localisation of caveolin in deep caveolae and its re-distribution after cholesterol depletion

1 reference

https://api.crossref.org/works/10.1161%2FCIRCULATIONAHA.106.635268

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1161%2FCIRCULATIONAHA.106.635268

7 January 2021

SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome

1 reference

https://api.crossref.org/works/10.1161%2FCIRCULATIONAHA.106.635268

7 January 2021

Identification and functional analysis of a caveolin-3 mutation associated with familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1161%2FCIRCULATIONAHA.106.635268

7 January 2021

Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism

1 reference

https://api.crossref.org/works/10.1161%2FCIRCULATIONAHA.106.635268

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1161%2FCIRCULATIONAHA.106.635268

7 January 2021

Long QT syndrome caused by a large duplication in the KCNH2 (HERG) gene undetectable by current polymerase chain reaction-based exon-scanning methodologies.

1 reference

https://api.crossref.org/works/10.1161%2FCIRCULATIONAHA.106.635268

7 January 2021

Regulation of the voltage-gated cardiac sodium channel Nav1.5 by interacting proteins.

1 reference

https://api.crossref.org/works/10.1161%2FCIRCULATIONAHA.106.635268

7 January 2021

Cryptic 5' splice site activation in SCN5A associated with Brugada syndrome

1 reference

https://api.crossref.org/works/10.1161%2FCIRCULATIONAHA.106.635268

7 January 2021

Molecular biology and the prolonged QT syndromes

1 reference

https://api.crossref.org/works/10.1161%2FCIRCULATIONAHA.106.635268

7 January 2021

Molecular remodelling of dystrophin in patients with end-stage cardiomyopathies and reversal in patients on assistance-device therapy.

1 reference

https://api.crossref.org/works/10.1161%2FCIRCULATIONAHA.106.635268

7 January 2021

Cardiac conduction defects associate with mutations in SCN5A

1 reference

https://api.crossref.org/works/10.1161%2FCIRCULATIONAHA.106.635268

7 January 2021

Molecular mechanism for an inherited cardiac arrhythmia

1 reference

https://api.crossref.org/works/10.1161%2FCIRCULATIONAHA.106.635268

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1161%2FCIRCULATIONAHA.106.635268

7 January 2021

Mutations in the hminK gene cause long QT syndrome and suppress IKs function

1 reference

https://api.crossref.org/works/10.1161%2FCIRCULATIONAHA.106.635268

7 January 2021

Cardiac channelopathies: it's in the genes.

1 reference

https://api.crossref.org/works/10.1161%2FCIRCULATIONAHA.106.635268

7 January 2021

Assembly of a Ca2+-dependent BK channel signaling complex by binding to beta2 adrenergic receptor

1 reference

https://api.crossref.org/works/10.1161%2FCIRCULATIONAHA.106.635268

7 January 2021

Influence of the genotype on the clinical course of the long-QT syndrome. International Long-QT Syndrome Registry Research Group.

1 reference

https://api.crossref.org/works/10.1161%2FCIRCULATIONAHA.106.635268

7 January 2021

Localization of cardiac L-type Ca(2+) channels to a caveolar macromolecular signaling complex is required for beta(2)-adrenergic regulation

1 reference

https://api.crossref.org/works/10.1161%2FCIRCULATIONAHA.106.635268

7 January 2021

Differential targeting of beta -adrenergic receptor subtypes and adenylyl cyclase to cardiomyocyte caveolae. A mechanism to functionally regulate the cAMP signaling pathway

1 reference

https://api.crossref.org/works/10.1161%2FCIRCULATIONAHA.106.635268

7 January 2021

Isoform-specific localization of voltage-gated K+ channels to distinct lipid raft populations. Targeting of Kv1.5 to caveolae

1 reference

https://api.crossref.org/works/10.1161%2FCIRCULATIONAHA.106.635268

7 January 2021

Genetic and biophysical basis of sudden unexplained nocturnal death syndrome (SUNDS), a disease allelic to Brugada syndrome

1 reference

https://api.crossref.org/works/10.1161%2FCIRCULATIONAHA.106.635268

7 January 2021

Caveolin-3 in muscular dystrophy

1 reference

https://api.crossref.org/works/10.1161%2FCIRCULATIONAHA.106.635268

7 January 2021

Molecular biology of arrhythmic syndromes

1 reference

https://api.crossref.org/works/10.1161%2FCIRCULATIONAHA.106.635268

7 January 2021

The cardiac sodium-calcium exchanger associates with caveolin-3.

1 reference

https://api.crossref.org/works/10.1161%2FCIRCULATIONAHA.106.635268

7 January 2021

A beta2 adrenergic receptor signaling complex assembled with the Ca2+ channel Cav1.2

1 reference

https://api.crossref.org/works/10.1161%2FCIRCULATIONAHA.106.635268

7 January 2021

Gaining Respectability

1 reference

https://api.crossref.org/works/10.1161%2FCIRCULATIONAHA.106.635268

7 January 2021

Contribution of sodium channel mutations to bradycardia and sinus node dysfunction in LQT3 families

1 reference

https://api.crossref.org/works/10.1161%2FCIRCULATIONAHA.106.635268

7 January 2021

A ubiquitous splice variant and a common polymorphism affect heterologous expression of recombinant human SCN5A heart sodium channels

1 reference

https://api.crossref.org/works/10.1161%2FCIRCULATIONAHA.106.635268

7 January 2021

Localization of pacemaker channels in lipid rafts regulates channel kinetics

1 reference

https://api.crossref.org/works/10.1161%2FCIRCULATIONAHA.106.635268

7 January 2021

Common sodium channel promoter haplotype in asian subjects underlies variability in cardiac conduction.

1 reference

https://api.crossref.org/works/10.1161%2FCIRCULATIONAHA.106.635268

7 January 2021

A CAV3 microdeletion differentially affects skeletal muscle and myocardium

1 reference

https://api.crossref.org/works/10.1161%2FCIRCULATIONAHA.106.635268

7 January 2021