The long QT syndrome family of cardiac ion channelopathies: a HuGE review. - Wikidata - awgldk - TriplyDB

The long QT syndrome family of cardiac ion channelopathies: a HuGE review.

The long QT syndrome family of cardiac ion channelopathies: a HuGE review.

http://www.wikidata.org/entity/Q33153638

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Impaired endocytosis of the ion channel TRPM4 is associated with human progressive familial heart block type I Coupling Data Mining and Laboratory Experiments to Discover Drug Interactions Causing QT Prolongation Increased vulnerability of human ventricle to re-entrant excitation in hERG-linked variant 1 short QT syndrome Relationship between genetic variants in myocardial sodium and potassium channel genes and QT interval duration in diabetics: the Diabetes Heart Study Cardiac models in drug discovery and development: a review.Congenital long QT syndromes: clinical features, molecular genetics and genetic testing.Genetic testing for long QT syndrome and the category of cardiac ion channelopathies.Beyond the Electrocardiogram: Mutations in Cardiac Ion Channel Genes Underlie Nonarrhythmic Phenotypes.A novel genetic modifier for clarithromycin-related cardiac arrhythmia risk?The impact of patents on the development of genome-based clinical diagnostics: an analysis of case studies.Drug-induced QT interval prolongation: mechanisms and clinical management Prevention of torsade de pointes in hospital settings: a scientific statement from the American Heart Association and the American College of Cardiology Foundation.Mendelian-inherited heart disease: a gateway to understanding mechanisms in heart disease Update on work done at the University of Stellenbosch Perceptions of an implantable cardioverter-defibrillator: A qualitative study of families with a history of sudden life-threatening cardiac events and recommendations to improve care.Action potential clamp and pharmacology of the variant 1 Short QT Syndrome T618I hERG K⁺ channel.Protein kinase A activity at the endoplasmic reticulum surface is responsible for augmentation of human ether-a-go-go-related gene product (HERG).Channelopathies: summary of the hot topic keynotes session The use of Bcl-2 over-expression to stabilize hybridomas specific to the HERG potassium channel Primary hyperparathyroidism and its management in a woman with hereditary long QT syndrome.Post-transcriptional regulation of cardiac sodium channel gene SCN5A expression and function by miR-192-5p Dysfunctional potassium channel subunit interaction as a novel mechanism of long QT syndrome.Requisite Role of Kv1.5 Channels in Coronary Metabolic Dilation.Phenotypic variability in Caucasian and Japanese patients with matched LQT1 mutations.Predict, prevent and personalize: Genomic and proteomic approaches to cardiovascular medicine Family history: an essential tool for cardiovascular genetic medicine.The new biology: a bridge to clinical cardiology.Review and management of the dental patient with Long QT syndrome (LQTS).Modification by KCNE1 variants of the hERG potassium channel response to premature stimulation and to pharmacological inhibition.Race and gender representation of hypertrophic cardiomyopathy or long QT syndrome cases in a South African research setting.miRNA in the regulation of ion channel/transporter expression.Association between CACNA1C gene polymorphisms and ritodrine-induced adverse events in preterm labor patients.The hERG K(+) channel S4 domain L532P mutation: characterization at 37°C Acute effects of ethanol on action potential and intracellular Ca(2+) transient in cardiac ventricular cells: a simulation study.An Isoform of Nedd4-2 Plays a Pivotal Role in Electrophysiological Cardiac Abnormalities.Suppression of the hERG potassium channel response to premature stimulation by reduction in extracellular potassium concentration.International Life Sciences Institute (Health and Environmental Sciences Institute, HESI) initiative on moving towards better predictors of drug-induced torsades de pointes.Predicting the Functional Impact of KCNQ1 Variants of Unknown Significance.Genomic-based diagnosis of arrhythmia disease in a personalized medicine era.Antiarrhythmic properties of a rapid delayed-rectifier current activator in rabbit models of acquired long QT syndrome.Differential roles of two delayed rectifier potassium currents in regulation of ventricular action potential duration and arrhythmia susceptibility.

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The long QT syndrome family of cardiac ion channelopathies: a HuGE review.

http://www.wikidata.org/entity/Q33153638

description

2006 nî lūn-bûn

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2006 թուականի Մարտին հրատարակուած գիտական յօդուած

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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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The long QT syndrome family of cardiac ion channelopathies: a HuGE review.

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The long QT syndrome family of cardiac ion channelopathies: a HuGE review.

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The long QT syndrome family of cardiac ion channelopathies: a HuGE review.

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The long QT syndrome family of cardiac ion channelopathies: a HuGE review.

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The long QT syndrome family of cardiac ion channelopathies: a HuGE review.

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P2860

KCNQ1 gain-of-function mutation in familial atrial fibrillation

Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2

A novel long-QT 5 gene mutation in the C-terminus (V109I) is associated with a mild phenotype

Congenital sick sinus syndrome caused by recessive mutations in the cardiac sodium channel gene (SCN5A)

A common human SCN5A polymorphism modifies expression of an arrhythmia causing mutation.

Asthma and the risk of cardiac events in the Long QT syndrome. Long QT Syndrome Investigative Group.

Inherited long QT syndromes: a paradigm for understanding arrhythmogenesis.

Genotype-phenotype correlation in the long-QT syndrome: gene-specific triggers for life-threatening arrhythmias.

Bradycardia-induced long QT syndrome caused by a de novo missense mutation in the S2-S3 inner loop of HERG.

Long QT syndrome in children: the value of the rate corrected QT interval in children who present with fainting.

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