Acute and subacute effects of the selective serotonin-noradrenaline reuptake inhibitor duloxetine on cardiac hERG channels.

about

Inhibition of cardiac Kv1.5 potassium current by the anesthetic midazolam: mode of action.Anesthetic drug midazolam inhibits cardiac human ether-à-go-go-related gene channels: mode of action Cardiovascular adverse effects of newer antidepressants.

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P2860

Acute and subacute effects of the selective serotonin-noradrenaline reuptake inhibitor duloxetine on cardiac hERG channels.

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Acute and subacute effects of ...... tine on cardiac hERG channels.

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P2860

A mechanistic link between an inherited and an acquired cardiac arrhythmia: HERG encodes the IKr potassium channel

A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome

A structural basis for drug-induced long QT syndrome

HERG1 channelopathies

Inhibition of G protein-activated inwardly rectifying K+ channels by different classes of antidepressants.

Cardiac ion channels.

Anticholinergic antiparkinson drug orphenadrine inhibits HERG channels: block attenuation by mutations of the pore residues Y652 or F656.

Genetic defects of cardiac ion channels. The hidden substrate for torsades de pointes.

Relationships between preclinical cardiac electrophysiology, clinical QT interval prolongation and torsade de pointes for a broad range of drugs: evidence for a provisional safety margin in drug development.

Drug-induced long QT syndrome: hERG K+ channel block and disruption of protein trafficking by fluoxetine and norfluoxetine.

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Acute and subacute effects of the selective serotonin-noradrenaline reuptake inhibitor duloxetine on cardiac hERG channels.

about

P2860

P2860

Acute and subacute effects of the selective serotonin-noradrenaline reuptake inhibitor duloxetine on cardiac hERG channels.

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