Mutant caveolin-3 induces persistent late sodium current and is associated with long-QT syndrome
about
Novel mechanism for sudden infant death syndrome: persistent late sodium current secondary to mutations in caveolin-3Sudden infant death syndrome-associated mutations in the sodium channel beta subunitsMutation of an A-kinase-anchoring protein causes long-QT syndromeSyntrophin mutation associated with long QT syndrome through activation of the nNOS-SCN5A macromolecular complexSCN4B-encoded sodium channel beta4 subunit in congenital long-QT syndromeGPD1L links redox state to cardiac excitability by PKC-dependent phosphorylation of the sodium channel SCN5ACaveolinopathies: from the biology of caveolin-3 to human diseasesSpectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION long QT syndrome genetic testPathogenesis of lethal cardiac arrhythmias in Mecp2 mutant mice: implication for therapy in Rett syndromeMolecular 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 familyGenetics of channelopathies associated with sudden cardiac deathGenetics of inherited primary arrhythmia disordersThe role of late I Na in development of cardiac arrhythmiasLong-QT syndrome: from genetics to managementChannelopathies from mutations in the cardiac sodium channel protein complexMolecular and genetic basis of sudden cardiac deathIon Channels in the HeartProtein assemblies of sodium and inward rectifier potassium channels control cardiac excitability and arrhythmogenesisRegulation of intracellular Na(+) in health and disease: pathophysiological mechanisms and implications for treatmentThe late Na+ current--origin and pathophysiological relevanceDefective 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 FibrosisThe role of the SCN5A-encoded channelopathy in irritable bowel syndrome and other gastrointestinal disordersIon channel macromolecular complexes in cardiomyocytes: roles in sudden cardiac deathIdentification of a Kir3.4 mutation in congenital long QT syndromeCaveolin regulates endocytosis of the muscle repair protein, dysferlinPost-translational modifications of the cardiac Na channel: contribution of CaMKII-dependent phosphorylation to acquired arrhythmiasA novel and lethal de novo LQT-3 mutation in a newborn with distinct molecular pharmacology and therapeutic responseα1-Syntrophin Variant Identified in Drug-Induced Long QT Syndrome Increases Late Sodium CurrentThe interaction of caveolin 3 protein with the potassium inward rectifier channel Kir2.1: physiology and pathology related to long qt syndrome 9 (LQT9)Caveolae in ventricular myocytes are required for stretch-dependent conduction slowingCongenital 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.The coiled-coil domain of MURC/cavin-4 is involved in membrane trafficking of caveolin-3 in cardiomyocytes.Role of risk stratification and genetics in sudden cardiac death.Sudden cardiac death prediction and prevention: report from a National Heart, Lung, and Blood Institute and Heart Rhythm Society Workshop.Clinical aspects of type-1 long-QT syndrome by location, coding type, and biophysical function of mutations involving the KCNQ1 gene.Sudden arrhythmic death syndrome: familial evaluation identifies inheritable heart disease in the majority of families.
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P2860
Mutant caveolin-3 induces persistent late sodium current and is associated with long-QT syndrome
description
2006 nî lūn-bûn
@nan
2006 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
Mutant caveolin-3 induces pers ...... sociated with long-QT syndrome
@ast
Mutant caveolin-3 induces pers ...... sociated with long-QT syndrome
@en
Mutant caveolin-3 induces pers ...... sociated with long-QT syndrome
@en-gb
Mutant caveolin-3 induces pers ...... sociated with long-QT syndrome
@nl
type
label
Mutant caveolin-3 induces pers ...... sociated with long-QT syndrome
@ast
Mutant caveolin-3 induces pers ...... sociated with long-QT syndrome
@en
Mutant caveolin-3 induces pers ...... sociated with long-QT syndrome
@en-gb
Mutant caveolin-3 induces pers ...... sociated with long-QT syndrome
@nl
prefLabel
Mutant caveolin-3 induces pers ...... sociated with long-QT syndrome
@ast
Mutant caveolin-3 induces pers ...... sociated with long-QT syndrome
@en
Mutant caveolin-3 induces pers ...... sociated with long-QT syndrome
@en-gb
Mutant caveolin-3 induces pers ...... sociated with long-QT syndrome
@nl
P2093
P921
P3181
P1433
P1476
Mutant caveolin-3 induces pers ...... sociated with long-QT syndrome
@en
P2093
David J Tester
Enoh E Ughanze
Erica W Taylor
Jason D Foell
Jonathan C Makielski
Matteo Vatta
Michael J Ackerman
Ravi C Balijepalli
Zhaohui Li
P304
P3181
P356
10.1161/CIRCULATIONAHA.106.635268
P407
P577
2006-11-14T00:00:00Z