Genetic basis and molecular mechanism for idiopathic ventricular fibrillation
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RYR2 sequencing reveals novel missense mutations in a Kazakh idiopathic ventricular tachycardia study cohortExome sequencing identifies a mutation in the ACTN2 gene in a family with idiopathic ventricular fibrillation, left ventricular noncompaction, and sudden deathBrugada syndromeFunctional consequences of a domain 1/S6 segment sodium channel mutation associated with painful congenital myotoniaMutation in glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) decreases cardiac Na+ current and causes inherited arrhythmiasIdentification of a new co-factor, MOG1, required for the full function of cardiac sodium channel Nav 1.5Identification of an angiogenic factor that when mutated causes susceptibility to Klippel-Trenaunay syndromeSodium channel β1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humansCorrelations between clinical and physiological consequences of the novel mutation R878C in a highly conserved pore residue in the cardiac Na+ channelMOG1 rescues defective trafficking of Na(v)1.5 mutations in Brugada syndrome and sick sinus syndromeGPD1L links redox state to cardiac excitability by PKC-dependent phosphorylation of the sodium channel SCN5ASolution NMR structure of the C-terminal EF-hand domain of human cardiac sodium channel NaV1.5The sodium channel beta-subunit SCN3b modulates the kinetics of SCN5a and is expressed heterogeneously in sheep heartScn3b knockout mice exhibit abnormal ventricular electrophysiological propertiesCharacterization of a new sodium channel mutation at arginine 1448 associated with moderate Paramyotonia congenita in humansFunctional effects of KCNE3 mutation and its role in the development of Brugada syndromeMolecular genetics of coronary artery diseaseLoss-of-function mutations in the cardiac calcium channel underlie a new clinical entity characterized by ST-segment elevation, short QT intervals, and sudden cardiac deathGenetic basis of Brugada syndromeAdvances in the genetic basis of coronary artery diseaseUse of intravenous antiarrhythmics to identify concealed Brugada syndromeRecurrent cardiac events in patients with idiopathic ventricular fibrillation, excluding patients with the Brugada syndromeTherapeutic Approaches to Genetic Ion Channelopathies and Perspectives in Drug DiscoveryThe Brugada Syndrome: A Rare Arrhythmia Disorder with Complex InheritanceConduction abnormalities and ventricular arrhythmogenesis: The roles of sodium channels and gap junctionsGenetics of channelopathies associated with sudden cardiac deathGenetics of inherited primary arrhythmia disordersReprogramming and transdifferentiation for cardiovascular development and regenerative medicine: where do we stand?Molecular and genetic basis of sudden cardiac deathIon Channels in the HeartProtein 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 channelopathiesCardiac disease and arrhythmogenesis: Mechanistic insights from mouse modelsInherited ion channel diseases: a brief reviewElectrophysiological Mechanisms of Brugada Syndrome: Insights from Pre-clinical and Clinical StudiesGenetics of Brugada syndromeClinical and Mechanistic Insights Into the Genetics of CardiomyopathyGain-of-function mutation S422L in the KCNJ8-encoded cardiac K(ATP) channel Kir6.1 as a pathogenic substrate for J-wave syndromesUnraveling the genetics and mechanisms of cardiac arrhythmia.Arrhythmia in heart and brain: KCNQ1 mutations link epilepsy and sudden unexplained death.
P2860
Q21131998-6E314DFC-EDAB-46A8-B248-E1A3D6019B10Q21146705-4C108767-7847-48C7-AA9D-1908B86F3B5DQ21203035-E0E2E8E5-72C4-4A47-9FE0-E1FEC956498FQ22009453-B5AAA0F0-C2D0-4A92-B43B-404481E6A375Q24298971-47A6B544-F00A-4E27-A50F-220608F5EEA6Q24306114-9FE6C228-DCCA-4A2F-B743-119C3B0D4457Q24307874-B0CD7D46-0BFC-4AB1-A480-358D2022382FQ24310498-E373D6A7-DA6C-4E4F-9C5E-D10A68B5475AQ24311774-3D236DED-3BC0-4E60-BE57-D876E16D9056Q24318749-0D96EB71-4FA2-4663-A5FA-E272BFC46D53Q24323030-3800A24F-7C12-4BFA-A7A9-0155AAF67C59Q24324607-A4724B32-EEF0-4694-8BB7-C68B121F0629Q24647082-AB2BF60E-B8DB-4A75-9AA1-AB453E8979A8Q24651316-E61E012A-58ED-4A15-946A-018090B05BEDQ24651364-872771B0-537B-4454-916D-DFB95A038465Q24655604-04C74409-7B4D-400E-862B-527D13B7F105Q24674808-5F08D225-E448-4357-AB61-56451C364ED6Q24675134-81798F2D-5684-4D52-9E61-696398A92F1EQ24681917-060801DB-5C84-4D19-970C-2563C4D25F28Q24682029-AED8B555-2A2F-4FDE-A41F-3A721DE43019Q24792476-1C6ED248-03CC-4F6B-8B8F-7C8138A8327DQ24808740-A41F9997-5362-4C26-98F9-6BE1DD7A46E8Q26744730-81F9EABC-3F1E-4A4D-91FB-118DF3B2FBF5Q26747227-7F4BD337-8632-47DC-A56F-FB9076E426E7Q26769921-FB7C5285-621C-4495-8E80-7E1B5BBA9FF0Q26777170-36139C10-76AC-4990-83A5-A510467B6520Q26783570-C1AB151F-8810-4C2F-9211-6BB6583F7949Q26800082-DDEA5077-337F-4796-8A00-73C6288F5011Q26825973-CD1B490E-6358-4DB4-A6E8-CBB417FCCEAEQ26829681-21E0DD6C-E60E-4691-9F76-A38519B8B4B1Q26830051-8D9229EB-1498-4984-964E-844EAF667E83Q26866107-C137E981-5713-474D-BCDC-FA2740FF269EQ28066019-14443DC8-EA99-4193-A01D-1FE39F7FF7E7Q28071914-D8407FE8-191F-43DD-8711-0D29F2EEA46BQ28073629-651F9633-DB4D-48DC-AE74-E00AC3BFD066Q28074918-AD0FA9C7-2801-4507-B752-CDD2FB3747F3Q28075470-335143DF-C72D-4579-86EA-B396836A4149Q28118815-E3A272E5-6BB0-4531-8977-4EF1AF594CF9Q28216187-6CC08332-2DA3-4535-9A71-42390E2B0149Q28278686-3BEAE118-DC93-426A-B367-24FCC55FF705
P2860
Genetic basis and molecular mechanism for idiopathic ventricular fibrillation
description
1998 nî lūn-bûn
@nan
1998 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի մարտին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
Genetic basis and molecular mechanism for idiopathic ventricular fibrillation
@ast
Genetic basis and molecular mechanism for idiopathic ventricular fibrillation
@en
Genetic basis and molecular mechanism for idiopathic ventricular fibrillation
@nl
type
label
Genetic basis and molecular mechanism for idiopathic ventricular fibrillation
@ast
Genetic basis and molecular mechanism for idiopathic ventricular fibrillation
@en
Genetic basis and molecular mechanism for idiopathic ventricular fibrillation
@nl
prefLabel
Genetic basis and molecular mechanism for idiopathic ventricular fibrillation
@ast
Genetic basis and molecular mechanism for idiopathic ventricular fibrillation
@en
Genetic basis and molecular mechanism for idiopathic ventricular fibrillation
@nl
P2093
P2860
P3181
P356
P1433
P1476
Genetic basis and molecular mechanism for idiopathic ventricular fibrillation
@en
P2093
E Schulze-Bahr
G Breithardt
G E Kirsch
J A Towbin
M Borggrefe
M T Keating
P2860
P2888
P3181
P356
10.1038/32675
P407
P577
1998-03-19T00:00:00Z
P5875
P6179
1019489151