Pages that link to "Q37019675"

The following pages link to Divergent biophysical defects caused by mutant sodium channels in dilated cardiomyopathy with arrhythmia (Q37019675):

Displaying 35 items.

• Multifocal ectopic Purkinje-related premature contractions: a new SCN5A-related cardiac channelopathy (Q24339527) (← links)
• Cellular hyper-excitability caused by mutations that alter the activation process of voltage-gated sodium channels (Q27008161) (← links)
• Aberrant sodium influx causes cardiomyopathy and atrial fibrillation in mice (Q27329882) (← links)
• Fibroblast growth factor homologous factor 13 regulates Na+ channels and conduction velocity in murine hearts (Q28118243) (← links)
• Targeted analysis of whole genome sequence data to diagnose genetic cardiomyopathy (Q30847057) (← links)
• LQTS mutation N1325S in cardiac sodium channel gene SCN5A causes cardiomyocyte apoptosis, cardiac fibrosis and contractile dysfunction in mice (Q33157825) (← links)
• Voltage-gated sodium channels were differentially expressed in human normal prostate, benign prostatic hyperplasia and prostate cancer cells (Q33778333) (← links)
• Cardiac sodium channelopathies (Q33906972) (← links)
• Novel SCN5A mutation in amiodarone-responsive multifocal ventricular ectopy-associated cardiomyopathy (Q33940611) (← links)
• A proton leak current through the cardiac sodium channel is linked to mixed arrhythmia and the dilated cardiomyopathy phenotype (Q34295483) (← links)
• Pathological role of serum- and glucocorticoid-regulated kinase 1 in adverse ventricular remodeling. (Q34302400) (← 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)
• Augmented Rififylin Is a Risk Factor Linked to Aberrant Cardiomyocyte Function, Short-QT Interval and Hypertension (Q34694622) (← links)
• Deletion of PDK1 causes cardiac sodium current reduction in mice (Q35188267) (← links)
• Developmentally regulated SCN5A splice variant potentiates dysfunction of a novel mutation associated with severe fetal arrhythmia (Q35798904) (← links)
• Striking In vivo phenotype of a disease-associated human SCN5A mutation producing minimal changes in vitro (Q35816436) (← links)
• Changes in Intracellular Na+ following Enhancement of Late Na+ Current in Virtual Human Ventricular Myocytes (Q36201210) (← 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)
• Gating pore current is a novel biophysical defect of Nav1.5 mutations associated with unusual cardiac arrhythmias and dilation (Q38506245) (← links)
• The cardiac sodium channel gene SCN5A and its gene product NaV1.5: Role in physiology and pathophysiology. (Q38585131) (← links)
• Nav 1.5 mutations linked to dilated cardiomyopathy phenotypes: Is the gating pore current the missing link? (Q40402516) (← links)
• Gating pore currents, a new pathological mechanism underlying cardiac arrhythmias associated with dilated cardiomyopathy. (Q41277802) (← links)
• Aberrant sialylation causes dilated cardiomyopathy and stress-induced heart failure (Q41466008) (← links)
• CaMKII modulates sodium current in neurons from epileptic Scn2a mutant mice (Q42219555) (← links)
• Mutations in the Voltage Sensors of Domains I and II of Nav1.5 that are Associated with Arrhythmias and Dilated Cardiomyopathy Generate Gating Pore Currents. (Q43110938) (← links)
• Molecular and Functional Changes in Voltage-Gated Na+ Channels in Cardiomyocytes During Mouse Embryogenesis (Q45910529) (← links)
• A New Cardiac Channelopathy: From Clinical Phenotypes to Molecular Mechanisms Associated With Na1.5 Gating Pores (Q57816587) (← links)
• Gating Pore Currents in Sodium Channels (Q58327238) (← links)
• A common polymorphism in the SCN5A gene is associated with dilated cardiomyopathy (Q88755888) (← links)
• Roles for Countercharge in the Voltage Sensor Domain of Ion Channels (Q90379579) (← links)
• Cardiac Sodium Channel Dysfunction and Dilated Cardiomyopathy: A Contemporary Reappraisal of Pathophysiological Concepts (Q92129342) (← links)
• Role of the voltage sensor module in Nav domain IV on fast inactivation in sodium channelopathies: The implication of closed-state inactivation (Q92259842) (← links)
• A combination of quinidine/mexiletine reduces arrhythmia in dilated cardiomyopathy in two patients with R814W SCN5A mutation (Q100754373) (← links)