Vincenzo Barrese

St George's University Of London
London, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 38 publications

The fast-dissociating D2 antagonist antipsychotic JNJ-37822681 is a neuronal Kv7 channel opener: Potential repurposing for epilepsy treatment.

The fast-dissociating D2 antagonist antipsychotic JNJ-37822681 is a neuronal Kv7 channel opener: Potential repurposing for epilepsy treatment.

Journal: British journal of pharmacology

Published: December 23, 2024

Constitutive opening of the Kv7.2 pore activation gate causes KCNQ2-developmental encephalopathy.

Constitutive opening of the Kv7.2 pore activation gate causes KCNQ2-developmental encephalopathy.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: November 27, 2024

Crucial role for sensory nerves and Na/H exchanger inhibition in dapagliflozin- and empagliflozin-induced arterial relaxation.

Crucial role for sensory nerves and Na/H exchanger inhibition in dapagliflozin- and empagliflozin-induced arterial relaxation.

Journal: Cardiovascular research

Published: March 19, 2024

Kv7 channel activation reduces brain endothelial cell permeability and prevents kainic acid-induced blood-brain barrier damage.

Kv7 channel activation reduces brain endothelial cell permeability and prevents kainic acid-induced blood-brain barrier damage.

Journal: American journal of physiology. Cell physiology

Published: January 29, 2024

Crucial role for Sodium Hydrogen Exchangers in SGLT2 inhibitor-induced arterial relaxations.

Crucial role for Sodium Hydrogen Exchangers in SGLT2 inhibitor-induced arterial relaxations.

Journal: bioRxiv : the preprint server for biology

Published: December 20, 2023

Beyond Retigabine: Design, Synthesis, and Pharmacological Characterization of a Potent and Chemically Stable Neuronal Kv7 Channel Activator with Anticonvulsant Activity.

Beyond Retigabine: Design, Synthesis, and Pharmacological Characterization of a Potent and Chemically Stable Neuronal Kv7 Channel Activator with Anticonvulsant Activity.

Journal: Journal of medicinal chemistry

Published: August 16, 2022

Key role for Kv11.1 (ether-a-go-go related gene) channels in rat bladder contractility.

Key role for Kv11.1 (ether-a-go-go related gene) channels in rat bladder contractility.

Journal: Physiological reports

Published: August 12, 2022

Gain of function due to increased opening probability by two KCNQ5 pore variants causing developmental and epileptic encephalopathy.

Gain of function due to increased opening probability by two KCNQ5 pore variants causing developmental and epileptic encephalopathy.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: April 04, 2022

Kv7.2 and Kv7.3 potassium channel subunits as new central regulators of blood pressure.

Kv7.2 and Kv7.3 potassium channel subunits as new central regulators of blood pressure.

Journal: Cardiovascular research

Published: January 20, 2022

Marked oestrous cycle-dependent regulation of rat arterial KV 7.4 channels driven by GPER1.

Marked oestrous cycle-dependent regulation of rat arterial KV 7.4 channels driven by GPER1.

Journal: British journal of pharmacology

Published: November 14, 2021

Kv7.4 channels regulate potassium permeability in neuronal mitochondria.

Kv7.4 channels regulate potassium permeability in neuronal mitochondria.

Journal: Biochemical pharmacology

Published: October 21, 2021

Editorial: Kv7 Channels: Structure, Physiology, and Pharmacology.

Editorial: Kv7 Channels: Structure, Physiology, and Pharmacology.

Journal: Frontiers in physiology

Published: March 11, 2021

Showing 1-12 of 38

Last Updated: 09/26/2026