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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.Frontiers in Systems Neuroscience|July 5, 2016
Intrinsic Hippocampal Excitability Changes of Opposite Signs and Different Origins in CA1 and CA3 Pyramidal Neurons Underlie Aging-Related Cognitive DeficitsM Matthew Oh, Dina Simkin, John F DisterhoftHuman Molecular Genetics|September 11, 2014
The inward rectifier potassium channel Kir2.1 is required for osteoblastogenesisSonia Sacco, Serena Giuliano, Sabrina Sacconi, et al.Brain Research|March 18, 2006
Evaluation of HCN2 abnormalities as a cause of juvenile audiogenic seizures in Black Swiss miceMinyoung Shin, Dina Simkin, Genn M Suyeoka, 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.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.Pageof 5