A mechanism for sudden infant death syndrome (SIDS): stress-induced leak via ryanodine receptors.
about
Sudden infant death syndrome-associated mutations in the sodium channel beta subunitsSudden unexplained death in infants and children: the role of undiagnosed inherited cardiac conditionsThe RYR2-encoded ryanodine receptor/calcium release channel in patients diagnosed previously with either catecholaminergic polymorphic ventricular tachycardia or genotype negative, exercise-induced long QT syndrome: a comprehensive open reading framExome Analyses of Long QT Syndrome Reveal Candidate Pathogenic Mutations in Calmodulin-Interacting GenesInfection: the neglected paradigm in SIDS researchSudden Unexpected Death in Fetal Life Through Early ChildhoodLeaky Ca2+ release channel/ryanodine receptor 2 causes seizures and sudden cardiac death in mice.Part 10: Pediatric basic and advanced life support: 2010 International Consensus on Cardiopulmonary Resuscitation and Emergency Cardiovascular Care Science With Treatment Recommendations.Short-coupled polymorphic ventricular tachycardia at rest linked to a novel ryanodine receptor (RyR2) mutation: leaky RyR2 channels under non-stress conditions.Alpha1-syntrophin mutations identified in sudden infant death syndrome cause an increase in late cardiac sodium currentA common single nucleotide polymorphism can exacerbate long-QT type 2 syndrome leading to sudden infant death.The ryanodine receptor in cardiac physiology and disease.Endoplasmic reticulum Ca(2+) handling in excitable cells in health and diseaseGene expression analysis characterizes antemortem stress and has implications for establishing cause of death.Loss-of-function mutations in the KCNJ8-encoded Kir6.1 K(ATP) channel and sudden infant death syndrome.Connexin43 mutation causes heterogeneous gap junction loss and sudden infant deathState of postmortem genetic testing known as the cardiac channel molecular autopsy in the forensic evaluation of unexplained sudden cardiac death in the young.A mechanistic description of gating of the human cardiac ryanodine receptor in a regulated minimal environment.Cardiac ion channelopathies and the sudden infant death syndromeOverrepresentation of the proarrhythmic, sudden death predisposing sodium channel polymorphism S1103Y in a population-based cohort of African-American sudden infant death syndrome.Pediatric basic and advanced life support: 2010 International Consensus on Cardiopulmonary Resuscitation and Emergency Cardiovascular Care Science with Treatment Recommendations.Sudden infant death syndrome: do ion channels play a role?LQTS-associated mutation A257G in α1-syntrophin interacts with the intragenic variant P74L to modify its biophysical phenotype.Sudden infant death syndrome in mice with an inherited mutation in RyR2.Ryanodine receptor mutations in arrhythmia: The continuing mystery of channel dysfunction.Gene variants predisposing to SIDS: current knowledge.Cardiac channelopathies and sudden infant death syndrome.Intact numbers of cerebellar purkinje and granule cells in sudden infant death syndrome: a stereologic analysis and critical review of neuropathologic evidence.Sudden cardiac death in the young: the molecular autopsy and a practical approach to surviving relatives.Sudden infant death syndrome caused by cardiac arrhythmias: only a matter of genes encoding ion channels?Advances in the diagnosis and treatment of catecholaminergic polymorphic ventricular tachycardia.Beyond the cardiac myofilament: hypertrophic cardiomyopathy- associated mutations in genes that encode calcium-handling proteins.A novel ryanodine receptor mutation linked to sudden death increases sensitivity to cytosolic calcium.Just sinus bradycardia or something more serious?Integration of 60,000 exomes and ACMG guidelines question the role of Catecholaminergic Polymorphic Ventricular Tachycardia-associated variants.Physiology and pathophysiology of excitation-contraction coupling: the functional role of ryanodine receptor.Sudden infant death syndrome and inherited cardiac conditions.Structural heterogeneity promotes triggered activity, reflection and arrhythmogenesis in cardiomyocyte monolayers.Postmortem genetic testing of the ryanodine receptor 2 (RYR2) gene in a cohort of sudden unexplained death cases.Genetic analysis of sudden cardiac death victims: a survey of current forensic autopsy practices.
P2860
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P2860
A mechanism for sudden infant death syndrome (SIDS): stress-induced leak via ryanodine receptors.
description
2007 nî lūn-bûn
@nan
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
2007年论文
@zh
2007年论文
@zh-cn
name
A mechanism for sudden infant ...... leak via ryanodine receptors.
@ast
A mechanism for sudden infant ...... leak via ryanodine receptors.
@en
type
label
A mechanism for sudden infant ...... leak via ryanodine receptors.
@ast
A mechanism for sudden infant ...... leak via ryanodine receptors.
@en
prefLabel
A mechanism for sudden infant ...... leak via ryanodine receptors.
@ast
A mechanism for sudden infant ...... leak via ryanodine receptors.
@en
P2093
P2860
P1433
P1476
A mechanism for sudden infant ...... leak via ryanodine receptors.
@en
P2093
Andrew R Marks
Anetta Wronska
David J Tester
Elisa Carturan
Michael J Ackerman
Miroslav Dura
Steven Reiken
P2860
P304
P356
10.1016/J.HRTHM.2007.02.026
P577
2007-03-03T00:00:00Z