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Stem Cells (Dayton, Ohio)|September 25, 2016
Depletion of the Fragile X Mental Retardation Protein in Embryonic Stem Cells Alters the Kinetics of NeurogenesisOlfa Khalfallah, Marielle Jarjat, Laetitia Davidovic, et al.
Human Mutation|April 30, 2009
A rescuable folding defective Nav1.1 (SCN1A) sodium channel mutant causes GEFS+: common mechanism in Nav1.1 related epilepsies?Raffaella Rusconi, Romina Combi, Sandrine Cestèle, et al.
Toxicon : Official Journal of the International Society on Toxinology|January 24, 2007
Voltage-gated ion channels and gating modifier toxinsWilliam A Catterall, Sandrine Cestèle, Vladimir Yarov-Yarovoy, et al.
Epilepsia|February 13, 2013
Divergent effects of the T1174S SCN1A mutation associated with seizures and hemiplegic migraineSandrine Cestèle, Angelo Labate, Raffaella Rusconi, et al.
The Journal of Clinical Investigation|September 7, 2021
Initiation of migraine-related cortical spreading depolarization by hyperactivity of GABAergic neurons and NaV1.1 channelsOana Chever, Sarah Zerimech, Paolo Scalmani, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 28, 2024
Brainstem depolarization-induced lethal apnea associated with gain-of-function SCN1AL263V is prevented by sodium channel blockadeNico A Jansen, Sandrine Cestèle, Silvia Sanchez Marco, et al.
Epilepsia|August 1, 2013
Loss-of-function KCNH2 mutation in a family with long QT syndrome, epilepsy, and sudden deathSara Partemi, Sandrine Cestèle, Marianna Pezzella, et al.
Journal of Peptide Science : an Official Publication of the European Peptide Society|December 1, 2004
First chemical synthesis of a scorpion alpha-toxin affecting sodium channels: the Aah I toxin of Androctonus australis hectorSarrah M'Barek, Ziad Fajloun, Sandrine Cestèle, et al.
Neurology. Genetics|April 27, 2026
Elicited Repetitive Daily Blindness Associated With Gain-of-Function SCN1A Variants and Responsiveness to Sodium Channel BlockersSandrine Cestèle, Alexander James Harper, Sebastian Marra, et al.
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