Sodium channel β1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans
about
Loss-of-function mutation of the SCN3B-encoded sodium channel {beta}3 subunit associated with a case of idiopathic ventricular fibrillationA connexin40 mutation associated with a malignant variant of progressive familial heart block type ISudden infant death syndrome-associated mutations in the sodium channel beta subunitsCrystallographic insights into sodium-channel modulation by the β4 subunitImpaired endocytosis of the ion channel TRPM4 is associated with human progressive familial heart block type IMexiletine differentially restores the trafficking defects caused by two brugada syndrome mutationsMutations in sodium channel β1- and β2-subunits associated with atrial fibrillationGPD1L links redox state to cardiac excitability by PKC-dependent phosphorylation of the sodium channel SCN5AScn3b knockout mice exhibit abnormal ventricular electrophysiological propertiesThe Brugada Syndrome: A Rare Arrhythmia Disorder with Complex InheritanceGenetics of channelopathies associated with sudden cardiac deathGenetics of inherited primary arrhythmia disordersEarly repolarization syndrome: A cause of sudden cardiac deathChannelopathies from mutations in the cardiac sodium channel protein complexMolecular and genetic basis of sudden cardiac deathIon Channels in the HeartJ-wave syndromes: Brugada and early repolarization syndromesInherited bradyarrhythmia: A diverse genetic backgroundElectrophysiological Mechanisms of Brugada Syndrome: Insights from Pre-clinical and Clinical StudiesGenetics of Brugada syndromeOn the multiple roles of the voltage gated sodium channel β1 subunit in genetic diseasesSodium channel β subunits: emerging targets in channelopathiesChannelopathies of skeletal muscle excitabilityThe cardiac conduction systemVariants of Transient Receptor Potential Melastatin Member 4 in Childhood Atrioventricular BlockScn3b knockout mice exhibit abnormal sino-atrial and cardiac conduction propertiesAxon initial segment dysfunction in a mouse model of genetic epilepsy with febrile seizures plus.Distinct functional defect of three novel Brugada syndrome related cardiac sodium channel mutationsAccelerated inactivation of the L-type calcium current due to a mutation in CACNB2b underlies Brugada syndromeRisk Stratification and Therapeutic Approach in Brugada Syndrome.A mutation in the beta 3 subunit of the cardiac sodium channel associated with Brugada ECG phenotypeAbnormal repolarization as the basis for late potentials and fractionated electrograms recorded from epicardium in experimental models of Brugada syndrome.An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing.Functional reciprocity between Na+ channel Nav1.6 and beta1 subunits in the coordinated regulation of excitability and neurite outgrowth.J wave syndromes.Cardiac sodium channelopathies.Gain-of-function mutation in TASK-4 channels and severe cardiac conduction disorder.Dual variation in SCN5A and CACNB2b underlies the development of cardiac conduction disease without Brugada syndrome.SCN5A mutations in Brugada syndrome are associated with increased cardiac dimensions and reduced contractility.Empiric quinidine therapy for asymptomatic Brugada syndrome: time for a prospective registry.
P2860
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P2860
Sodium channel β1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans
description
2008 nî lūn-bûn
@nan
2008 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
Sodium channel β1 subunit muta ...... c conduction disease in humans
@ast
Sodium channel β1 subunit muta ...... c conduction disease in humans
@en
Sodium channel β1 subunit muta ...... c conduction disease in humans
@en-gb
Sodium channel β1 subunit muta ...... c conduction disease in humans
@nl
type
label
Sodium channel β1 subunit muta ...... c conduction disease in humans
@ast
Sodium channel β1 subunit muta ...... c conduction disease in humans
@en
Sodium channel β1 subunit muta ...... c conduction disease in humans
@en-gb
Sodium channel β1 subunit muta ...... c conduction disease in humans
@nl
prefLabel
Sodium channel β1 subunit muta ...... c conduction disease in humans
@ast
Sodium channel β1 subunit muta ...... c conduction disease in humans
@en
Sodium channel β1 subunit muta ...... c conduction disease in humans
@en-gb
Sodium channel β1 subunit muta ...... c conduction disease in humans
@nl
P2093
P2860
P50
P921
P3181
P356
P1476
Sodium channel β1 subunit muta ...... c conduction disease in humans
@en
P2093
Ans C P Wiesfeld
Can Hasdemir
Christiana R Ingram
Connie R Bezzina
Dan M Roden
Frédéric Anselme
Hiroshi Watanabe
Sophie Demolombe
Tamara T Koopmann
P2860
P304
P3181
P356
10.1172/JCI33891
P407
P50
P577
2008-06-01T00:00:00Z