Pages that link to "Q39977115"

The following pages link to Molecular and clinical characterization of a novel SCN5A mutation associated with atrioventricular block and dilated cardiomyopathy (Q39977115):

Displaying 34 items.

• Physiological and Pathophysiological Insights of Nav1.4 and Nav1.5 Comparison (Q26772794) (← links)
• Cellular hyper-excitability caused by mutations that alter the activation process of voltage-gated sodium channels (Q27008161) (← links)
• SCN5A mutation in Chinese patients with arrhythmogenic right ventricular dysplasia (Q33163606) (← links)
• Cardiac sodium channelopathies (Q33906972) (← links)
• A Proton Leak Current through the Cardiac Sodium Channel Is Linked to Mixed Arrhythmia and the Dilated Cardiomyopathy Phenotype (Q34295483) (← links)
• Sodium MRI in human heart: a review (Q34462810) (← links)
• SCN5A Rare Variants in Familial Dilated Cardiomyopathy Decrease Peak Sodium Current Depending on the Common Polymorphism H558R and Common Splice Variant Q1077del (Q34517554) (← links)
• The genetic basis for inherited forms of sinoatrial dysfunction and atrioventricular node dysfunction (Q35800619) (← links)
• Striking In vivo phenotype of a disease-associated human SCN5A mutation producing minimal changes in vitro (Q35816436) (← links)
• Cardiac Nav 1.5 is modulated by ubiquitin protein ligase E3 component n-recognin UBR3 and 6. (Q36057480) (← links)
• A1180V of cardiac sodium channel gene (SCN5A): is it a risk factor for dilated cardiomyopathy or just a common variant in Han Chinese? (Q37280116) (← links)
• Sodium channel mutations and arrhythmias (Q37450777) (← links)
• Mouse Models of SCN5A-Related Cardiac Arrhythmias (Q38022001) (← links)
• Cardiac sodium channelopathy associated with SCN5A mutations: electrophysiological, molecular and genetic aspects (Q38118751) (← links)
• Biophysics, pathophysiology, and pharmacology of ion channel gating pores (Q38207583) (← links)
• Reduced Penetrance and Variable Expression of SCN5A Mutations and the Importance of Co-inherited Genetic Variants: Case Report and Review of the Literature. (Q38221847) (← links)
• Cardiac sodium channels and inherited electrophysiological disorders: an update on the pharmacotherapy (Q38225937) (← links)
• Sodium channel haploinsufficiency and structural change in ventricular arrhythmogenesis (Q38568991) (← links)
• Murine Electrophysiological Models of Cardiac Arrhythmogenesis (Q39038606) (← links)
• Analysis of SCN5A Gene Variants in East Slovak Patients with Cardiomyopathy. (Q39460292) (← links)
• Nav 1.5 mutations linked to dilated cardiomyopathy phenotypes: Is the gating pore current the missing link? (Q40402516) (← links)
• Aberrant sialylation causes dilated cardiomyopathy and stress-induced heart failure (Q41466008) (← links)
• Genetic Mechanisms Contribute to the Development of Heart Failure in Patients with Atrioventricular Block and Right Ventricular Apical Pacing (Q41633912) (← links)
• Wnt signalling suppresses voltage-dependent Na⁺ channel expression in postnatal rat cardiomyocytes (Q41643746) (← links)
• The Connexin40A96S mutation from a patient with atrial fibrillation causes decreased atrial conduction velocities and sustained episodes of induced atrial fibrillation in mice. (Q44672435) (← links)
• Isolated Left Atrial Standstill Identified during Catheter Ablation (Q45987297) (← links)
• The SCN5A mutation A1180V is associated with electrocardiographic features of LQT3. (Q46367175) (← links)
• Editor's Highlight: The Altered DNA Methylome of Chronic Doxorubicin Exposure in Sprague Dawley Rats (Q47666634) (← links)
• Variants: Association With Cardiac Disorders (Q58578329) (← links)
• Quantitative trait loci for electrocardiographic parameters and arrhythmia in the mouse (Q63359102) (← links)
• Protein structure aids predicting functional perturbation of missense variants in and (Q64264242) (← links)
• A common polymorphism in the SCN5A gene is associated with dilated cardiomyopathy (Q88755888) (← links)
• Reevaluating the Mutation Classification in Genetic Studies of Bradycardia Using ACMG/AMP Variant Classification Framework (Q90643495) (← links)
• Cardiac Sodium Channel Dysfunction and Dilated Cardiomyopathy: A Contemporary Reappraisal of Pathophysiological Concepts (Q92129342) (← links)