Inherited conduction system abnormalities--one group of diseases, many genes
about
Abnormal conduction and morphology in the atrioventricular node of mice with atrioventricular canal targeted deletion of Alk3/Bmpr1a receptorErbb2 is required for cardiac atrial electrical activity during developmentTissue distribution and subcellular localization of the cardiac sodium channel during mouse heart developmentLethal arrhythmias in Tbx3-deficient mice reveal extreme dosage sensitivity of cardiac conduction system function and homeostasisPerinatal loss of Nkx2-5 results in rapid conduction and contraction defectsCommon variants in 22 loci are associated with QRS duration and cardiac ventricular conduction.Whole-exome sequencing to identify a novel LMNA gene mutation associated with inherited cardiac conduction diseaseThe ionic bases of the action potential in isolated mouse cardiac Purkinje cellEfficient Generation of Cardiac Purkinje Cells from ESCs by Activating cAMP Signaling.The genetic basis for inherited forms of sinoatrial dysfunction and atrioventricular node dysfunctionThe primary arrhythmia syndromes: same mutation, different manifestations. Are we starting to understand why?Genetic basis of malignant channelopathies and ventricular fibrillation in the structurally normal heart.Cardiac sodium channelopathy associated with SCN5A mutations: electrophysiological, molecular and genetic aspects.Evaluation and management of bradycardia in neonates and children.Genetic isolation of stem cell-derived pacemaker-nodal cardiac myocytes.Islet1 is a direct transcriptional target of the homeodomain transcription factor Shox2 and rescues the Shox2-mediated bradycardia.Cardiac-specific overexpression of SCN5A gene leads to shorter P wave duration and PR interval in transgenic mice.Executive summary: HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes.Spatially resolved RNA-sequencing of the embryonic heart identifies a role for Wnt/β-catenin signaling in autonomic control of heart rate.Lineages of the Cardiac Conduction System.Inducible recombination in the cardiac conduction system of minK: CreERT² BAC transgenic mice.Executive Summary: HRS/EHRA/APHRS Expert Consensus Statement on the Diagnosis and Management of Patients with Inherited Primary Arrhythmia SyndromesHRS/EHRA/APHRS Expert Consensus Statement on the Diagnosis and Management of Patients with Inherited Primary Arrhythmia SyndromesElectrocardiogram changes and atrial arrhythmias in individuals carrying sodium channel SCN5A D1275N mutationThe Medical Management of Pediatric Arrhythmias
P2860
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P2860
Inherited conduction system abnormalities--one group of diseases, many genes
description
2006 nî lūn-bûn
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2006 թուականի Ապրիլին հրատարակուած գիտական յօդուած
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2006 թվականի ապրիլին հրատարակված գիտական հոդված
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2006年の論文
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2006年論文
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2006年論文
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2006年論文
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2006年論文
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2006年論文
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2006年论文
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Inherited conduction system abnormalities--one group of diseases, many genes
@ast
Inherited conduction system abnormalities--one group of diseases, many genes
@en
Inherited conduction system abnormalities--one group of diseases, many genes
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Inherited conduction system abnormalities--one group of diseases, many genes
@ast
Inherited conduction system abnormalities--one group of diseases, many genes
@en
Inherited conduction system abnormalities--one group of diseases, many genes
@nl
prefLabel
Inherited conduction system abnormalities--one group of diseases, many genes
@ast
Inherited conduction system abnormalities--one group of diseases, many genes
@en
Inherited conduction system abnormalities--one group of diseases, many genes
@nl
P2860
P1476
Inherited conduction system abnormalities--one group of diseases, many genes
@en
P2093
Charles I Berul
Cordula M Wolf
P2860
P304
P356
10.1111/J.1540-8167.2006.00427.X
P407
P577
2006-04-01T00:00:00Z