Sudden infant death syndrome-associated mutations in the sodium channel beta subunits - Test2 - elhamkhani - TriplyDB

Sudden infant death syndrome-associated mutations in the sodium channel beta subunits

Sudden infant death syndrome-associated mutations in the sodium channel beta subunits

http://www.wikidata.org/entity/Q24302400

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Crystallographic insights into sodium-channel modulation by the β4 subunit Inherited arrhythmias: The cardiac channelopathies The role of late I Na in development of cardiac arrhythmias Channelopathies from mutations in the cardiac sodium channel protein complex Sudden unexplained death in infants and children: the role of undiagnosed inherited cardiac conditions Protein assemblies of sodium and inward rectifier potassium channels control cardiac excitability and arrhythmogenesis Crystal Structure and Molecular Imaging of the Nav Channel 3 Subunit Indicates a Trimeric Assembly Sodium channel β subunits: emerging targets in channelopathies Congenital Long QT Syndrome: An Update and Present Perspective in Saudi Arabia.Role of risk stratification and genetics in sudden cardiac death.Digenic inheritance novel mutations in SCN5a and SNTA1 increase late I(Na) contributing to LQT syndrome.Fetal cardiac arrhythmia detection and in utero therapy Genomic risk factors in sudden infant death syndrome Functional dominant-negative mutation of sodium channel subunit gene SCN3B associated with atrial fibrillation in a Chinese GeneID population Na Channel β Subunits: Overachievers of the Ion Channel Family.A novel rare variant in SCN1Bb linked to Brugada syndrome and SIDS by combined modulation of Na(v)1.5 and K(v)4.3 channel currents.Cardiac ion channelopathies and the sudden infant death syndrome Binary architecture of the Nav1.2-β2 signaling complex Caveolin-3 suppresses late sodium current by inhibiting nNOS-dependent S-nitrosylation of SCN5A.Embryonic type Na+ channel β-subunit, SCN3B masks the disease phenotype of Brugada syndrome.Developmental changes in expression and biophysics of ion channels in the canine ventricle.SCN4B acts as a metastasis-suppressor gene preventing hyperactivation of cell migration in breast cancer Sudden infant death syndrome due to long QT syndrome: a brief review of the genetic substrate and prevalence.Cardiac channelopathies and sudden infant death syndrome.Neurological perspectives on voltage-gated sodium channels.A new look at sodium channel β subunits Molecular Pathophysiology of Congenital Long QT Syndrome.Murine Electrophysiological Models of Cardiac Arrhythmogenesis.Parallel homodimer structures of the extracellular domains of the voltage-gated sodium channel β4 subunit explain its role in cell-cell adhesion.Sudden infant death syndrome, sleep, and seizures.Investigations of the Navβ1b sodium channel subunit in human ventricle; functional characterization of the H162P Brugada syndrome mutant.Singular localization of sodium channel β4 subunit in unmyelinated fibres and its role in the striatum.Voltage-Gated Sodium Channel β Subunits and Their Related Diseases.Infant sudden death: Mutations responsible for impaired Nav1.5 channel trafficking and function.Voltage-gated sodium channel β subunits: The power outside the pore in brain development and disease.Sudden infant death syndrome and inherited cardiac conditions.Cardiac channelopathies associated with infantile fatal ventricular arrhythmias: from the cradle to the bench.Dysfunction of NaV1.4, a skeletal muscle voltage-gated sodium channel, in sudden infant death syndrome: a case-control study.Functional implications of a rare variant in the sodium channel β1B subunit (SCN1B) in a 5-month-old male sudden infant death syndrome case.Variants: Association With Cardiac Disorders

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P2860

Sudden infant death syndrome-associated mutations in the sodium channel beta subunits

http://www.wikidata.org/entity/Q24302400

description

2010 nî lūn-bûn

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2010 թուականի Յունիսին հրատարակուած գիտական յօդուած

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2010 թվականի հունիսին հրատարակված գիտական հոդված

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2010年の論文

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2010年论文

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Sudden infant death syndrome-associated mutations in the sodium channel beta subunits

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Sudden infant death syndrome-associated mutations in the sodium channel beta subunits

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Sudden infant death syndrome-associated mutations in the sodium channel beta subunits

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Sudden infant death syndrome-associated mutations in the sodium channel beta subunits

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type

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Sudden infant death syndrome-associated mutations in the sodium channel beta subunits

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Sudden infant death syndrome-associated mutations in the sodium channel beta subunits

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Sudden infant death syndrome-associated mutations in the sodium channel beta subunits

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Sudden infant death syndrome-associated mutations in the sodium channel beta subunits

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Sudden infant death syndrome-associated mutations in the sodium channel beta subunits

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Sudden infant death syndrome-associated mutations in the sodium channel beta subunits

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Sudden infant death syndrome-associated mutations in the sodium channel beta subunits

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Sudden infant death syndrome-associated mutations in the sodium channel beta subunits

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J.HRTHM.2010.01.032

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Sudden infant death syndrome-associated mutations in the sodium channel beta subunits

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Bi-Hua Tan

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Carmen R Valdivia

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David J Tester

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David W Van Norstrand

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Jonathan C Makielski

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Kavitha N Pundi

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Michael J Ackerman

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P2860

Loss-of-function mutation of the SCN3B-encoded sodium channel {beta}3 subunit associated with a case of idiopathic ventricular fibrillation

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

Mutation in glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) decreases cardiac Na+ current and causes inherited arrhythmias

Syntrophin mutation associated with long QT syndrome through activation of the nNOS-SCN5A macromolecular complex

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

Sodium channel β1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans

SCN4B-encoded sodium channel beta4 subunit in congenital long-QT syndrome

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

Nav1.5 E1053K mutation causing Brugada syndrome blocks binding to ankyrin-G and expression of Nav1.5 on the surface of cardiomyocytes

Mutations in sodium channel β1- and β2-subunits associated with atrial fibrillation

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771-778

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scholarly article

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3307585

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10.1016/J.HRTHM.2010.01.032

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6

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Argelia Medeiros-domingo

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2010-02-01T00:00:00Z

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41942415

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20226894

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membrane depolarization during action potential

Sodium voltage-gated channel beta subunit 3

Sodium voltage-gated channel beta subunit 4

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2909680

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