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Plos One|October 31, 2012
The inhibition of KCa3.1 channels activity reduces cell motility in glioblastoma derived cancer stem cellsPaola Ruggieri, Giorgio Mangino, Bernard Fioretti, et al.American Journal of Physiology. Cell Physiology|April 16, 2010
CXCL12-induced glioblastoma cell migration requires intermediate conductance Ca2+-activated K+ channel activityMiriam Sciaccaluga, Bernard Fioretti, Luigi Catacuzzeno, et al.Plos One|May 20, 2016
A Calsequestrin-1 Mutation Associated with a Skeletal Muscle Disease Alters Sarcoplasmic Ca2+ ReleaseMaria Cristina D'Adamo, Luigi Sforna, Sergio Visentin, et al.Human Molecular Genetics|February 25, 2016
Megalencephalic leukoencephalopathy with subcortical cysts protein-1 regulates epidermal growth factor receptor signaling in astrocytesAngela Lanciotti, Maria Stefania Brignone, Sergio Visentin, et al.Frontiers in Physiology|February 3, 2015
Novel phenotype associated with a mutation in the KCNA1(Kv1.1) geneMaria C D'Adamo, Constanze Gallenmüller, Ilenio Servettini, et al.Scientific Reports|September 29, 2016
Gain-of-function defects of astrocytic Kir4.1 channels in children with autism spectrum disorders and epilepsyFederico Sicca, Elena Ambrosini, Maria Marchese, et al.Human Molecular Genetics|May 6, 2014
Genetically induced dysfunctions of Kir2.1 channels: implications for short QT3 syndrome and autism-epilepsy phenotypeElena Ambrosini, Federico Sicca, Maria S Brignone, et al.Pageof 6