Kv11.1
2538 literature references associated to Kv11.1
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Activation of hERG3 channel stimulates autophagy and promotes cellular senescence in melanoma.
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Comparison between Hodgkin-Huxley and Markov formulations of cardiac ion channels.
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Histone Deacetylase Inhibitors Prolong Cardiac Repolarization through Transcriptional Mechanisms.
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Tyrosine residues from the S4-S5 linker of Kv11.1 channels are critical for slow deactivation.
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Molecular Basis of Cardiac Delayed Rectifier Potassium Channel Function and Pharmacology.
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Investigation of miscellaneous hERG inhibition in large diverse compound collection using automated patch-clamp assay.
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An evaluation of 30 clinical drugs against the comprehensive in vitro proarrhythmia assay (CiPA) proposed ion channel panel.
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The Scorpion Toxin Analogue BmKTX-D33H as a Potential Kv1.3 Channel-Selective Immunomodulator for Autoimmune Diseases.
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Autonomous beating rate adaptation in human stem cell-derived cardiomyocytes.
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Molecular basis and drug sensitivity of the delayed rectifier (IKr) in the fish heart.
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Transmural dispersion of repolarization and cardiac remodeling in ventricles of rabbit with right ventricular hypertrophy.
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In response to Melgari et al. "hERG potassium channel inhibition by ivabradine requires channel gating".
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hERG potassium channel inhibition by ivabradine requires channel gating.
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New echocardiographic insights in short QT syndrome: More than a channelopathy?
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Mechanism of inhibition by olanzapine of cloned hERG potassium channels.
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Regulation of the human ether-a-go-go-related gene (hERG) potassium channel by Nedd4 family interacting proteins (Ndfips).
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A Novel Pyrazolopyridine with in Vivo Activity in Plasmodium berghei- and Plasmodium falciparum-Infected Mouse Models from Structure-Activity Relationship Studies around the Core of Recently Identified Antimalarial Imidazopyridazines.
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Hypaconitine-induced QT prolongation mediated through inhibition of KCNH2 (hERG) potassium channels in conscious dogs.
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High-performance beating pattern function of human induced pluripotent stem cell-derived cardiomyocyte-based biosensors for hERG inhibition recognition.
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Cardiac Mechanical Alterations and Genotype Specific Differences in Subjects With Long QT Syndrome.
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Antiarrhythmic ionic mechanism of Guanfu base A--Selective inhibition of late sodium current in isolated ventricular myocytes from guinea pigs.
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Analysis for Genetic Modifiers of Disease Severity in Patients with Long QT Syndrome Type 2.
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Getting to the heart of hERG K(+) channel gating.
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Heterogeneous Phenotype of Long QT Syndrome Caused by the KCNH2-H562R Mutation: Importance of Familial Genetic Testing.
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Kinetic model for NS1643 drug activation of WT and L529I variants of Kv11.1 (hERG1) potassium channel.
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NS1643 interacts around L529 of hERG to alter voltage sensor movement on the path to activation.
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The interaction between delayed rectifier channel alpha-subunits does not involve hetero-tetramer formation.
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hERG1 channels drive tumour malignancy and may serve as prognostic factor in pancreatic ductal adenocarcinoma.
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Computational investigations of hERG channel blockers: New insights and current predictive models.
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Identification of drug targets related to the induction of ventricular tachyarrhythmia through a systems chemical biology approach.
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[Effects of midazolam on hERG K+ channel].
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Intravenous anesthetic propofol inhibits multiple human cardiac potassium channels.
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Functional Characterization of Rare Variants Implicated in Susceptibility to Lone Atrial Fibrillation.
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Two New Classes of T-Type Calcium Channel Inhibitors with New Chemical Scaffolds from Ganoderma cochlear.
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In silico investigation of PARP-1 catalytic domains in holo and apo states for the design of high-affinity PARP-1 inhibitors.
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Human Ether-à-go-go Related Gene (hERG) Channel Blocking Aporphine Alkaloids from Lotus Leaves and Their Quantitative Analysis in Dietary Weight Loss Supplements.
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The Link between Inactivation and High-Affinity Block of hERG1 Channels.
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Up-regulation of miR-21 and miR-23a Contributes to As2 O3 -induced hERG Channel Deficiency.
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Aromatase knockout mice reveal an impact of estrogen on drug-induced alternation of murine electrocardiography parameters.
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The cardiomyocyte molecular clock regulates the circadian expression of Kcnh2 and contributes to ventricular repolarization.
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Genetic screening in sudden cardiac death in the young can save future lives.
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Kcnh2 and Kcnj8 Interactively Regulate Skin Wound Healing and Regeneration.
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Pathogenesis of the Novel Autoimmune-Associated Long-QT Syndrome.
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hERG Channel Inhibitory Daphnane Diterpenoid Orthoesters and Polycephalones A and B with Unprecedented Skeletons from Gnidia polycephala.
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QT interval prolongation in a patient with LQT2 on levetiracetam.
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Characterization of a Chinese KCNQ1 mutation (R259H) that shortens repolarization and causes short QT syndrome 2.
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C-Linker Accounts for Differential Sensitivity of ERG1 and ERG2 K+ Channels to RPR260243-Induced Slow Deactivation.
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Arsenic trioxide inhibits breast cancer cell growth via microRNA-328/hERG pathway in MCF-7 cells.
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Genetic variants of potassium voltage-gated channel genes (KCNQ1, KCNH2, and KCNE1) affected the risk of atrial fibrillation in elderly patients.
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A novel pan-negative-gating modulator of KCa2/3 channels, fluoro-di-benzoate, RA-2, inhibits endothelium-derived hyperpolarization-type relaxation in coronary artery and produces bradycardia in vivo.
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Antipsychotic drugs and the risk of ventricular arrhythmia and/or sudden cardiac death: a nation-wide case-crossover study.
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