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Neuropharmacology|April 23, 2017
Effects of natural and synthetic isothiocyanate-based H2S-releasers against chemotherapy-induced neuropathic pain: Role of Kv7 potassium channelsLorenzo Di Cesare Mannelli, Elena Lucarini, Laura Micheli, et al.International Journal of Molecular Sciences|July 13, 2019
Epileptic Encephalopathy In A Patient With A Novel Variant In The Kv7.2 S2 Transmembrane Segment: Clinical, Genetic, and Functional FeaturesMaria Virginia Soldovieri, Paolo Ambrosino, Ilaria Mosca, et al.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.Journal of Molecular Biology|May 27, 2014
The ever changing moods of calmodulin: how structural plasticity entails transductional adaptabilityAlvaro Villarroel, Maurizio Taglialatela, Ganeko Bernardo-Seisdedos, 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.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.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.Pageof 13