Genetically induced dysfunctions of Kir2.1 channels: implications for short QT3 syndrome and autism–epilepsy phenotypeElena Ambrosini, Mauro Pessia, Federico Sicca et al.|Human Molecular Genetics|2014Cited by 85
The Inhibition of KCa3.1 Channels Activity Reduces Cell Motility in Glioblastoma Derived Cancer Stem CellsPaola Ruggieri, Antonella Calogero, Giorgio Mangino et al.|PLoS ONE|2012Cited by 82
Gain-of-function defects of astrocytic Kir4.1 channels in children with autism spectrum disorders and epilepsyFederico Sicca, Mauro Pessia, Elena Ambrosini et al.|Scientific Reports|2016Cited by 74
The CaMKII/MLC1 Axis Confers Ca2+-Dependence to Volume-Regulated Anion Channels (VRAC) in AstrocytesMaria Stefania Brignone, Elena Ambrosini, Angela Lanciotti et al.|Cells|2022Cited by 14
MLC1: A New Calcium-regulated Protein Conferring Calcium Dependence to Volume-regulated Anion Channels (VRAC) in Astrocytes.Maria Stefania Brignone, Elena Ambrosini, Angela Lanciotti et al.|Research Square|2022Cited by 1