Jolien De Waele

Jette, BRU, Belgium

Last Updated: 09/26/2026

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Found 8 publications

A neurocutaneous NaV1.8 channelopathy underlies a genetic subtype of primary idiopathic hyperhidrosis.

A neurocutaneous NaV1.8 channelopathy underlies a genetic subtype of primary idiopathic hyperhidrosis.

Journal: Science advances

Published: July 17, 2026

Differential regulation of β1-dependent voltage shifts and kinetic modulation by an extracellular glutamate in NaV1.6 VSDIV.

Differential regulation of β1-dependent voltage shifts and kinetic modulation by an extracellular glutamate in NaV1.6 VSDIV.

Journal: The Journal of general physiology

Published: March 30, 2026

Gene expression, purification, and functional characterization of recombinant conotoxin μ-TIIIA and TIIIAlaMut in Escherichia coli with clinical evaluation of antiwrinkle efficacy.

Gene expression, purification, and functional characterization of recombinant conotoxin μ-TIIIA and TIIIAlaMut in Escherichia coli with clinical evaluation of antiwrinkle efficacy.

Journal: Biotechnologia

Published: September 09, 2025

A robust expression system reveals distinct gating mechanisms and calmodulin regulation of NaV1.9 channels.

A robust expression system reveals distinct gating mechanisms and calmodulin regulation of NaV1.9 channels.

Journal: Science advances

Published: May 28, 2025

Structure-function relationship of new peptides activating human Nav1.1.

Structure-function relationship of new peptides activating human Nav1.1.

Journal: Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie

Published: March 23, 2023

N-Type Inactivation Variances in Honeybee and Asian Giant Hornet Kv Channels.

N-Type Inactivation Variances in Honeybee and Asian Giant Hornet Kv Channels.

Journal: Bioelectricity

Published: September 08, 2022

Biophysical Investigation of Sodium Channel Interaction with β-Subunit Variants Associated with Arrhythmias.

Biophysical Investigation of Sodium Channel Interaction with β-Subunit Variants Associated with Arrhythmias.

Journal: Bioelectricity

Published: September 03, 2021

Homozygous SCN1B variants causing early infantile epileptic encephalopathy 52 affect voltage-gated sodium channel function.

Homozygous SCN1B variants causing early infantile epileptic encephalopathy 52 affect voltage-gated sodium channel function.

Journal: Epilepsia

Published: September 11, 2020

Showing 1-8 of 8

Last Updated: 09/26/2026