Novel mechanism for sudden infant death syndrome: persistent late sodium current secondary to mutations in caveolin-3
about
Sudden infant death syndrome-associated mutations in the sodium channel beta subunitsSyntrophin mutation associated with long QT syndrome through activation of the nNOS-SCN5A macromolecular complexGPD1L links redox state to cardiac excitability by PKC-dependent phosphorylation of the sodium channel SCN5ACaveolinopathies: from the biology of caveolin-3 to human diseasesMolecular and functional characterization of novel glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) mutations in sudden infant death syndromealpha-1-syntrophin mutation and the long-QT syndrome: a disease of sodium channel disruptionMolecular evolution of the junctophilin gene familyChannelopathies from mutations in the cardiac sodium channel protein complexSudden unexplained death in infants and children: the role of undiagnosed inherited cardiac conditionsProtein assemblies of sodium and inward rectifier potassium channels control cardiac excitability and arrhythmogenesisDefective interactions of protein partner with ion channels and transporters as alternative mechanisms of membrane channelopathiesPTRF/Cavin-1 Deficiency Causes Cardiac Dysfunction Accompanied by Cardiomyocyte Hypertrophy and Cardiac FibrosisIon channel macromolecular complexes in cardiomyocytes: roles in sudden cardiac deathα1-Syntrophin Variant Identified in Drug-Induced Long QT Syndrome Increases Late Sodium CurrentCongenital Long QT Syndrome: An Update and Present Perspective in Saudi Arabia.Caveolin-1 modulates cardiac gap junction homeostasis and arrhythmogenecity by regulating cSrc tyrosine kinase.Infection: the neglected paradigm in SIDS researchSudden Unexpected Death in Fetal Life Through Early ChildhoodPart 10: Pediatric basic and advanced life support: 2010 International Consensus on Cardiopulmonary Resuscitation and Emergency Cardiovascular Care Science With Treatment Recommendations.Identification of a novel KCNQ1 mutation associated with both Jervell and Lange-Nielsen and Romano-Ward forms of long QT syndrome in a Chinese family.Digenic inheritance novel mutations in SCN5a and SNTA1 increase late I(Na) contributing to LQT syndrome.Alpha1-syntrophin mutations identified in sudden infant death syndrome cause an increase in late cardiac sodium currentCaveolae, ion channels and cardiac arrhythmias.A common single nucleotide polymorphism can exacerbate long-QT type 2 syndrome leading to sudden infant death.Cardiac sodium channelopathies.Identification and functional analysis of a new putative caveolin-3 variant found in a patient with sudden unexplained deathRNAi-based gene therapy for dominant Limb Girdle Muscular Dystrophies.Defining a new paradigm for human arrhythmia syndromes: phenotypic manifestations of gene mutations in ion channel- and transporter-associated proteins.LQTS gene LOVD databaseGenomic risk factors in sudden infant death syndromeDiseases caused by mutations in Nav1.5 interacting proteinsPalmitate diet-induced loss of cardiac caveolin-3: a novel mechanism for lipid-induced contractile dysfunction.The genetic basis for inherited forms of sinoatrial dysfunction and atrioventricular node dysfunctionNav channel mechanosensitivity: activation and inactivation accelerate reversibly with stretch.Sudden infant death syndrome and long QT syndrome: the zealots versus the naysayers.State of postmortem genetic testing known as the cardiac channel molecular autopsy in the forensic evaluation of unexplained sudden cardiac death in the young.A mechanism for sudden infant death syndrome (SIDS): stress-induced leak via ryanodine receptors.Rippling muscle disease and facioscapulohumeral dystrophy-like phenotype in a patient carrying a heterozygous CAV3 T78M mutation and a D4Z4 partial deletion: Further evidence for "double trouble" overlapping syndromesCardiac ion channelopathies and the sudden infant death syndromeUnderdiagnosis of Conditions Associated with Sudden Cardiac Death in Children--Is it the Absence of a Comprehensive Screening Program or a True Low Prevalence?
P2860
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P2860
Novel mechanism for sudden infant death syndrome: persistent late sodium current secondary to mutations in caveolin-3
description
2007 nî lūn-bûn
@nan
2007 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
name
Novel mechanism for sudden inf ...... ary to mutations in caveolin-3
@ast
Novel mechanism for sudden inf ...... ary to mutations in caveolin-3
@en
Novel mechanism for sudden inf ...... ary to mutations in caveolin-3
@en-gb
Novel mechanism for sudden inf ...... ary to mutations in caveolin-3
@nl
type
label
Novel mechanism for sudden inf ...... ary to mutations in caveolin-3
@ast
Novel mechanism for sudden inf ...... ary to mutations in caveolin-3
@en
Novel mechanism for sudden inf ...... ary to mutations in caveolin-3
@en-gb
Novel mechanism for sudden inf ...... ary to mutations in caveolin-3
@nl
prefLabel
Novel mechanism for sudden inf ...... ary to mutations in caveolin-3
@ast
Novel mechanism for sudden inf ...... ary to mutations in caveolin-3
@en
Novel mechanism for sudden inf ...... ary to mutations in caveolin-3
@en-gb
Novel mechanism for sudden inf ...... ary to mutations in caveolin-3
@nl
P2093
P2860
P3181
P1433
P1476
Novel mechanism for sudden inf ...... ary to mutations in caveolin-3
@en
P2093
David J Tester
Jonathan C Makielski
Lisa B Cronk
Matteo Vatta
Michael J Ackerman
Toshihiko Kaku
P2860
P3181
P356
10.1016/J.HRTHM.2006.11.030
P407
P577
2007-02-01T00:00:00Z