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Frontiers in Pharmacology|January 11, 2020
Pharmacological Profile of the Sodium Current in Human Stem Cell-Derived Cardiomyocytes Compares to Heterologous Nav1.5+β1 ModelDieter V Van de Sande, Ivan Kopljar, Ard Teisman, et al.
The Journal of Biological Chemistry|November 10, 2010
The S4-S5 linker of KCNQ1 channels forms a structural scaffold with the S6 segment controlling gate closureAlain J Labro, Inge R Boulet, Frank S Choveau, et al.
International Journal of Biological Macromolecules|June 21, 2016
Dromedary immune response and specific Kv2.1 antibody generation using a specific immunization approachRym Hassiki, Alain J Labro, Zakaria Benlasfar, et al.
International Journal of Molecular Sciences|December 10, 2021
Developmental Toxicity and Biotransformation of Two Anti-Epileptics in Zebrafish Embryos and Early LarvaeChloé Bars, Jente Hoyberghs, Allan Valenzuela, et al.
Science Advances|September 16, 2022
The nonconducting W434F mutant adopts upon membrane depolarization an inactivated-like state that differs from wild-type Shaker-IR potassium channelsLaura Coonen, Evelyn Martinez-Morales, Dieter V Van De Sande, et al.
The Journal of Biological Chemistry|August 31, 2012
Dual effect of phosphatidylinositol (4,5)-bisphosphate PIP(2) on Shaker K(+) [corrected] channelsFayal Abderemane-Ali, Zeineb Es-Salah-Lamoureux, Lucie Delemotte, et al.
Channels (Austin, Tex.)|January 19, 2021
The resting membrane potential of hSC-CM in a syncytium is more hyperpolarised than that of isolated cellsDieter V Van de Sande, Ivan Kopljar, Alaerts Maaike, et al.
The Journal of Biological Chemistry|October 14, 2010
KCNQ1 channels voltage dependence through a voltage-dependent binding of the S4-S5 linker to the pore domainFrank S Choveau, Nicolas Rodriguez, Fayal Abderemane Ali, et al.
Cardiovascular Research|August 19, 2020
Impaired cytoplasmic domain interactions cause co-assembly defect and loss of function in the p.Glu293Lys KNCJ2 variant isolated from an Andersen-Tawil syndrome patientSzilvia Déri, János Borbás, Teodóra Hartai, et al.
Frontiers in Cardiovascular Medicine|August 28, 2020
Compound Heterozygous <i>SCN5A</i> Mutations in Severe Sodium Channelopathy With Brugada Syndrome: A Case ReportAleksandra Nijak, Alain J Labro, Hans De Wilde, et al.
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