SCN5A mutation associated with dilated cardiomyopathy, conduction disorder, and arrhythmia
about
Brugada syndromeA connexin40 mutation associated with a malignant variant of progressive familial heart block type IVoltage-gated ion channel dysfunction precedes cardiomyopathy development in the dystrophic heartCell membrane expression of cardiac sodium channel Na(v)1.5 is modulated by alpha-actinin-2 interactionMutations in sodium channel β1- and β2-subunits associated with atrial fibrillationGenetics of Human and Canine Dilated CardiomyopathyThe role of late I Na in development of cardiac arrhythmiasCellular hyper-excitability caused by mutations that alter the activation process of voltage-gated sodium channelsClinical and Mechanistic Insights Into the Genetics of CardiomyopathyThe role of the SCN5A-encoded channelopathy in irritable bowel syndrome and other gastrointestinal disordersCoding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathyArrhythmia-Induced Cardiomyopathies: Mechanisms, Recognition, and ManagementTissue distribution and subcellular localization of the cardiac sodium channel during mouse heart developmentOrdered assembly of the adhesive and electrochemical connections within newly formed intercalated disks in primary cultures of adult rat cardiomyocytesPerinatal loss of Nkx2-5 results in rapid conduction and contraction defectsComplexities of Genetic Testing in Familial Dilated CardiomyopathyImaging phenotype vs genotype in nonhypertrophic heritable cardiomyopathies: dilated cardiomyopathy and arrhythmogenic right ventricular cardiomyopathyAblation of Nkx2-5 at mid-embryonic stage results in premature lethality and cardiac malformationIs there an overlap between Brugada syndrome and arrhythmogenic right ventricular cardiomyopathy/dysplasia?The cardiac sodium channel mutation delQKP 1507-1509 is associated with the expanding phenotypic spectrum of LQT3, conduction disorder, dilated cardiomyopathy, and high incidence of youth sudden deathLQTS mutation N1325S in cardiac sodium channel gene SCN5A causes cardiomyocyte apoptosis, cardiac fibrosis and contractile dysfunction in miceWhole-exome sequencing identifies Y1495X of SCN5A to be associated with familial conduction disease and sudden death.Loss-of-Function SCN5A Mutations Associated With Sinus Node Dysfunction, Atrial Arrhythmias, and Poor Pacemaker CaptureCanine candidate genes for dilated cardiomyopathy: annotation of and polymorphic markers for 14 genes.Beyond the Electrocardiogram: Mutations in Cardiac Ion Channel Genes Underlie Nonarrhythmic Phenotypes.Genetics and Sinus Node Dysfunction.Multiple loss-of-function mechanisms contribute to SCN5A-related familial sick sinus syndrome.A novel GJA1 mutation causing familial oculodentodigital dysplasia with dilated cardiomyopathy and arrhythmiaCardiomyopathies: Evolution of pathogenesis concepts and potential for new therapies.Alternative splicing of the cardiac sodium channel creates multiple variants of mutant T1620K channels.Inherited disorders of voltage-gated sodium channels.Cardiac sodium channelopathies.Improved understanding of the pathophysiology of atrial fibrillation through the lens of discrete pathological pathwaysNovel SCN5A mutation in amiodarone-responsive multifocal ventricular ectopy-associated cardiomyopathy.Atrial fibrillation in congestive heart failure.Gain-of-function mutation in TASK-4 channels and severe cardiac conduction disorder.Association of 25 bp deletion in MYBPC3 gene with left ventricle dysfunction in coronary artery disease patients.Genetics of human cardiovascular diseaseA proton leak current through the cardiac sodium channel is linked to mixed arrhythmia and the dilated cardiomyopathy phenotype.Personalized medicine and atrial fibrillation: will it ever happen?
P2860
Q21203035-C20487D7-0A67-404D-90F2-84DD24004222Q24302041-807DCB4E-8FEA-4D5F-B12F-238DE2077F82Q24306601-6D6FB099-848D-452F-A2C4-9F0185AF39AEQ24322255-076FA126-14F0-40D1-A860-F43F40CC44C5Q24322712-58249D3C-3187-4006-86FE-10FC261CCEB5Q26798712-4D4BDEC5-C706-47A1-8356-A76DFF917A2AQ26823149-DA3FDA53-F0D8-4CF6-AAD9-EAEFB6CFC17FQ27008161-736D99A9-BBAF-4F33-BDCA-C874AE78EF55Q28075470-1F929E3D-2D76-412F-855D-8B7FFCD7F04EQ28081627-B034AE7D-B554-42F9-8F05-461EFA798BD0Q28243560-7DE097D9-BDF9-4B2D-82EA-EFCCDFBAB7E5Q28268244-FC1820D9-15E8-494B-99B4-D9A25F224866Q28509012-8233945D-D59F-4E95-B278-428937B53668Q28571997-B38702DA-9524-4FA7-BB0B-2CC7E30CE559Q28593447-6A6A8CFF-028E-4796-A281-DEC4E5FA49F9Q30277328-55BF1B4B-9F6C-458F-9312-AEE3B3FE2635Q30473247-CD3390F1-A4CE-4A1B-BA62-93DD9ECFCE4DQ30501669-8F7B53FA-CD20-4EDE-97DC-F3E5B6F4CFD2Q33152891-C67104B1-0EB3-40BD-8CF9-A86BE6074CF2Q33156531-3AB000B1-F453-459D-85A4-A8383978814AQ33157825-A829FBDC-8CEF-4ABA-B57E-F4E89E3516B0Q33164501-867CDE3C-BC9B-451E-8E06-907AEA265D3BQ33165910-F2E23A50-7EDF-4AB2-A9EB-DD3E64DAA015Q33303253-B6379DE8-03AA-40C0-BD9A-F3374D95ED84Q33565907-D76BD9DD-70BA-4477-BDEC-214D82F88A2AQ33585556-10E45CC4-DE8A-419A-B03E-3A1AFC9ED6B7Q33601521-6CF852DA-62A6-4A49-AE37-F64610B37DABQ33625438-9BD9AD93-8467-49FC-B656-0F52946FF3FAQ33812953-6C4B53D2-9C8B-41D3-8C0A-1C22BF0D9A29Q33892566-3B882A9F-445A-4554-B131-FD4445B71546Q33905815-63CD5CEE-1662-492B-A0E2-116807D72CFCQ33906972-5DB5189F-5FB8-442D-81E4-5444D4BCBA81Q33923776-BCC62C00-8B77-4A7E-8D16-8D6B0293E59DQ33940611-103832C2-864B-46E7-9068-9364BF91E56EQ33954432-DA8D4CC4-846B-4306-AE5E-B25D0EF67123Q33991477-E2931C8A-9D09-46E2-BE11-A530FC9CCA98Q34018918-7B89AD1F-57BC-4814-AD16-5B011841136FQ34261931-A996459D-FAC9-418D-A598-92527CD7B047Q34295483-03CDD4C5-BFC4-4A78-B6B6-0C93ABA3799FQ34501117-6E0DF78C-2EEC-483D-8C7D-640CE28DF5FE
P2860
SCN5A mutation associated with dilated cardiomyopathy, conduction disorder, and arrhythmia
description
2004 nî lūn-bûn
@nan
2004 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
name
SCN5A mutation associated with ...... ction disorder, and arrhythmia
@ast
SCN5A mutation associated with ...... ction disorder, and arrhythmia
@en
SCN5A mutation associated with ...... ction disorder, and arrhythmia
@nl
type
label
SCN5A mutation associated with ...... ction disorder, and arrhythmia
@ast
SCN5A mutation associated with ...... ction disorder, and arrhythmia
@en
SCN5A mutation associated with ...... ction disorder, and arrhythmia
@nl
prefLabel
SCN5A mutation associated with ...... ction disorder, and arrhythmia
@ast
SCN5A mutation associated with ...... ction disorder, and arrhythmia
@en
SCN5A mutation associated with ...... ction disorder, and arrhythmia
@nl
P2093
P3181
P1433
P1476
SCN5A mutation associated with ...... ction disorder, and arrhythmia
@en
P2093
Eugene Wolfel
Matthew R G Taylor
Pam R Fain
William P McNair
P304
P3181
P356
10.1161/01.CIR.0000144458.58660.BB
P407
P577
2004-10-12T00:00:00Z