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Frontiers in Pharmacology|October 22, 2011
Skeletal muscle na channel disordersDina Simkin, Saïd BendahhouBiochimica Et Biophysica Acta|April 20, 2007
Role of hydrophobic residues in the voltage sensors of the voltage-gated sodium channelSaïd Bendahhou, Andrias O O'Reilly, Hervé DuclohierStem Cells and Development|November 18, 2015
Modeling Andersen's Syndrome in Human Induced Pluripotent Stem CellsJonathan Pini, Matthieu Rouleau, Claude Desnuelle, et al.British Journal of Pharmacology|February 19, 2026
Opening closed inward rectifier potassium channel doorsAnna Stary-Weinzinger, Fabian Kaiser, Marcel A G van der Heyden, et al.International Journal of Molecular Sciences|October 2, 2020
First Evidence of Kv3.1b Potassium Channel Subtype Expression during Neuronal Serotonergic 1C11 Cell Line DevelopmentHager Tabka, Amani Cheikh, Sonia Maatoug, et al.Human Molecular Genetics|February 28, 2007
Corticosteroid-exacerbated symptoms in an Andersen's syndrome kindredSaïd Bendahhou, Emmanuel Fournier, Serge Gallet, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|May 30, 2018
Osteogenic and Chondrogenic Master Genes Expression Is Dependent on the Kir2.1 Potassium Channel Through the Bone Morphogenetic Protein PathwayJonathan Pini, Serena Giuliano, Julia Matonti, et al.Human Molecular Genetics|September 11, 2014
The inward rectifier potassium channel Kir2.1 is required for osteoblastogenesisSonia Sacco, Serena Giuliano, Sabrina Sacconi, et al.The Journal of Physiology|April 28, 2011
Mechanisms underlying a life-threatening skeletal muscle Na+ channel disorderDina Simkin, Isabelle Léna, Pierre Landrieu, et al.The Journal of Biological Chemistry|October 3, 2003
Defective potassium channel Kir2.1 trafficking underlies Andersen-Tawil syndromeSaïd Bendahhou, Matthew R Donaldson, Nikki M Plaster, et al.Pageof 4