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Nature Communications|February 4, 2026
Two-step voltage-sensor activation of the human KV7.4 channel and effect of a deafness-associated mutationMario Nappi, Damon J A Frampton, Ali S Kusay, et al.
International Journal of Molecular Sciences|September 7, 2019
Activation of Kv7 Potassium Channels Inhibits Intracellular Ca2+ Increases Triggered By TRPV1-Mediated Pain-Inducing Stimuli in F11 Immortalized Sensory NeuronsPaolo Ambrosino, Maria Virginia Soldovieri, Erika Di Zazzo, et al.
The Journal of Biological Chemistry|November 2, 2005
Decreased subunit stability as a novel mechanism for potassium current impairment by a KCNQ2 C terminus mutation causing benign familial neonatal convulsionsMaria Virginia Soldovieri, Pasqualina Castaldo, Luisa Iodice, et al.
Journal of the Peripheral Nervous System : JPNS|November 11, 2019
Insights into the pathogenesis of ATP1A1-related CMT disease using patient-specific iPSCsFiore Manganelli, Silvia Parisi, Maria Nolano, et al.
Scientific Reports|December 2, 2016
Early-onset epileptic encephalopathy caused by a reduced sensitivity of Kv7.2 potassium channels to phosphatidylinositol 4,5-bisphosphateMaria Virginia Soldovieri, Paolo Ambrosino, Ilaria Mosca, et al.
The Journal of Biological Chemistry|April 7, 2004
A novel hyperekplexia-causing mutation in the pre-transmembrane segment 1 of the human glycine receptor alpha1 subunit reduces membrane expression and impairs gating by agonistsPasqualina Castaldo, Patrizia Stefanoni, Francesco Miceli, et al.
Neurogenetics|October 20, 2005
Functional analysis of novel KCNQ2 and KCNQ3 gene variants found in a large pedigree with benign familial neonatal convulsions (BFNC)Maria T Bassi, Umberto Balottin, Chris Panzeri, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|May 4, 2007
Atypical gating of M-type potassium channels conferred by mutations in uncharged residues in the S4 region of KCNQ2 causing benign familial neonatal convulsionsMaria Virginia Soldovieri, Maria Roberta Cilio, Francesco Miceli, et al.
Epilepsia|November 19, 2016
Infantile spasms and encephalopathy without preceding neonatal seizures caused by KCNQ2 R198Q, a gain-of-function variantJohn J Millichap, Francesco Miceli, Michela De Maria, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|January 19, 2024
Phenotypic and functional assessment of two novel KCNQ2 gain-of-function variants Y141N and G239S and effects of amitriptyline treatmentAllan Bayat, Stefano Iavarone, Francesco Miceli, et al.
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