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European Journal of Medicinal Chemistry|October 8, 2013
Isoxazole derivatives as potent transient receptor potential melastatin type 8 (TRPM8) agonistsCarmine Ostacolo, Paolo Ambrosino, Roberto Russo, et al.
Epilepsia|December 20, 2014
A novel KCNQ3 mutation in familial epilepsy with focal seizures and intellectual disabilityFrancesco Miceli, Pasquale Striano, Maria Virginia Soldovieri, et al.
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.
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.
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 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.
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