Allocryptopine and benzyltetrahydropalmatine block hERG potassium channels expressed in HEK293 cells

Berberine elicits anti-arrhythmic effects via IK1/Kir2.1 in the rat type 2 diabetic myocardial infarction model.

Functional characterization of the LQT2-causing mutation R582C and the associated voltage-dependent fluorescence signal.

Ginsenoside Rg(3) decelerates hERG K(+) channel deactivation through Ser631 residue interaction.

Models of HERG gating.

The hERG K+ channel S4 domain L532P mutation: Characterization at 37 °C

hERG potassium channel gating is mediated by N- and C-terminal region interactions

Acidosis impairs the protective role of hERG K(+) channels against premature stimulation.

Investigating dynamic protocol-dependence of hERG potassium channel inhibition at 37 degrees C: Cisapride versus dofetilide.

QT alterations in psychopharmacology: proven candidates and suspects.

Comparative effects of the short QT N588K mutation at 37 degrees C on hERG K+ channel current during ventricular, Purkinje fibre and atrial action potentials: an action potential clamp study.

Allocryptopine and benzyltetrahydropalmatine block hERG potassium channels expressed in HEK293 cells

Shuyu Capsules Relieve Premenstrual Syndrome Depression by Reducing 5-HT3AR and 5-HT3BR Expression in the Rat Brain

Berberine elicits anti-arrhythmic effects via IK1/Kir2.1 in the rat type 2 diabetic myocardial infarction model.

Functional characterization of the LQT2-causing mutation R582C and the associated voltage-dependent fluorescence signal.

Ginsenoside Rg(3) decelerates hERG K(+) channel deactivation through Ser631 residue interaction.

Models of HERG gating.

The hERG K+ channel S4 domain L532P mutation: Characterization at 37 °C

hERG potassium channel gating is mediated by N- and C-terminal region interactions

Acidosis impairs the protective role of hERG K(+) channels against premature stimulation.

Investigating dynamic protocol-dependence of hERG potassium channel inhibition at 37 degrees C: Cisapride versus dofetilide.

QT alterations in psychopharmacology: proven candidates and suspects.

Comparative effects of the short QT N588K mutation at 37 degrees C on hERG K+ channel current during ventricular, Purkinje fibre and atrial action potentials: an action potential clamp study.

Allocryptopine and benzyltetrahydropalmatine block hERG potassium channels expressed in HEK293 cells

Shuyu Capsules Relieve Premenstrual Syndrome Depression by Reducing 5-HT3AR and 5-HT3BR Expression in the Rat Brain

Berberine elicits anti-arrhythmic effects via IK1/Kir2.1 in the rat type 2 diabetic myocardial infarction model.

Functional characterization of the LQT2-causing mutation R582C and the associated voltage-dependent fluorescence signal.

Ginsenoside Rg(3) decelerates hERG K(+) channel deactivation through Ser631 residue interaction.

Models of HERG gating.

The hERG K+ channel S4 domain L532P mutation: Characterization at 37 °C

hERG potassium channel gating is mediated by N- and C-terminal region interactions

Acidosis impairs the protective role of hERG K(+) channels against premature stimulation.

Investigating dynamic protocol-dependence of hERG potassium channel inhibition at 37 degrees C: Cisapride versus dofetilide.

QT alterations in psychopharmacology: proven candidates and suspects.

Comparative effects of the short QT N588K mutation at 37 degrees C on hERG K+ channel current during ventricular, Purkinje fibre and atrial action potentials: an action potential clamp study.