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The Journal of Biological Chemistry|December 5, 2009
Potassium channel silencing by constitutive endocytosis and intracellular sequestrationSylvain Feliciangeli, Magalie P Tardy, Guillaume Sandoz, et al.
Cell|August 19, 2007
Does sumoylation control K2P1/TWIK1 background K+ channels?Sylvain Feliciangeli, Saïd Bendahhou, Guillaume Sandoz, et al.
International Journal of Molecular Sciences|November 27, 2021
Cross Pharmacological, Biochemical and Computational Studies of a Human Kv3.1b Inhibitor from <i>Androctonus australis</i> VenomSonia Maatoug, Amani Cheikh, Oussema Khamessi, et al.
Cardiovascular Research|July 26, 2005
In vitro molecular interactions and distribution of KCNE family with KCNQ1 in the human heartSaïd Bendahhou, Céline Marionneau, Karinne Haurogne, et al.
Journal of Clinical Medicine|May 14, 2022
Relationships between Plasma Pyrophosphate, Vascular Calcification and Clinical Severity in Patients Affected by Pseudoxanthoma ElasticumGeorges Leftheriotis, Nastassia Navasiolava, Laetitia Clotaire, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 21, 2012
TWIK1, a unique background channel with variable ion selectivityFranck C Chatelain, Delphine Bichet, Dominique Douguet, et al.
Iscience|June 16, 2023
Biological fractionation of lithium isotopes by cellular Na<sup>+</sup>/H<sup>+</sup> exchangers unravels fundamental transport mechanismsMallorie Poet, Nathalie Vigier, Yann Bouret, et al.
Cell and Tissue Research|October 12, 2017
Andersen's syndrome mutants produce a knockdown of inwardly rectifying K<sup>+</sup> channel in mouse skeletal muscle in vivoDina Simkin, Gaëlle Robin, Serena Giuliano, et al.
Annals of Medicine|June 7, 2006
Molecular characterization of two founder mutations causing long QT syndrome and identification of compound heterozygous patientsHeidi Fodstad, Saïd Bendahhou, Jean-Sébastien Rougier, et al.
Scientific Reports|February 3, 2018
Substitutions of the S4DIV R2 residue (R1451) in Na<sub>V</sub>1.4 lead to complex forms of paramyotonia congenita and periodic paralysesHugo Poulin, Pascal Gosselin-Badaroudine, Savine Vicart, et al.
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