Alain J. Labro
Gent, VLG, Belgium
Last Updated: 09/26/2026
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Found 36 publications
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
Oxygen Handling Practices for in Vitro Human Pluripotent Stem Cell Cardiomyocyte Differentiation: A Scoping Literature Review.
Journal: Stem cell reviews and reports
Published: August 14, 2025
Evaluating the proarrhythmic risk of delayed-action compounds in serum free cell culture conditions; serum-starvation accelerates/amplifies the effect of probucol on the KCNQ1 + KCNE1 channel.
Journal: Journal of pharmacological and toxicological methods
Published: June 26, 2024
Immunosuppressive effects of new thiophene-based KV1.3 inhibitors.
Journal: European journal of medicinal chemistry
Published: January 19, 2023
A Possible Explanation for the Low Penetrance of Pathogenic KCNE1 Variants in Long QT Syndrome Type 5.
Journal: Pharmaceuticals (Basel, Switzerland)
Published: November 07, 2022
Correction: Gubič et al. Design of New Potent and Selective Thiophene-Based KV1.3 Inhibitors and Their Potential for Anticancer Activity. Cancers 2022, 14, 2595.
Journal: Cancers
Published: September 22, 2022
The nonconducting W434F mutant adopts upon membrane depolarization an inactivated-like state that differs from wild-type Shaker-IR potassium channels.
Journal: Science advances
Published: September 16, 2022
Clinical and functional characterisation of a recurrent KCNQ1 variant in the Belgian population.
Journal: Orphanet journal of rare diseases
Published: July 19, 2022
Developmental Toxicity and Biotransformation of Two Anti-Epileptics in Zebrafish Embryos and Early Larvae.
Journal: International journal of molecular sciences
Published: October 13, 2021
Morpho-functional comparison of differentiation protocols to create iPSC-derived cardiomyocytes.
Journal: Biology open
Published: September 02, 2021
Molecular autopsy and subsequent functional analysis reveal de novo DSG2 mutation as cause of sudden death.
Journal: European journal of medical genetics
Published: February 15, 2021
Last Updated: 09/26/2026