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Results 41-48 of 48 (Search time: 0.021 seconds).
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Issue DateTitleAuthor(s)
2015Animal models of episodic ataxia type 1 (EA1)D'Adamo, Maria Cristina; Di Giovanni, Giuseppe; Pessia, Mauro
2017Lethal digenic mutations in the K+ 1 channels Kir4.1 (KCNJ10) and SLACK 2 (KCNT1) associated with severe-disabling seizures and neurodevelopmental delayHasan, Sonia M.; Balobaid, Ameera; Grottesi, Alessandro; Dabbagh, Omar; Cenciarini, Marta; Rawashdeh, Rifaat; Al-Sagheir, Afaf; Bove, Cecilia; Macchioni, Lara; Pessia, Mauro; Al-Owain, Mohammed A.; D'Adamo, Maria Cristina
2014Role(s) of the 5-HT2C receptor in the development of maximal dentate activation in the hippocampus of anesthetized ratsOrban, Gergely; Bombardi, Cristiano; Marino Gammazza, Antonella; Colangeli, Roberto; Pierucci, Massimo; Pomara, Cristoforo; Pessia, Mauro; Bucchieri, Fabio; Arcangelo, Benigno; Smolders, Ilse J.; De Deurwaerdère, Philippe; Di Giovanni, Giuseppe
2003Functional characterization of an episodic ataxia type-1 mutation occurring in the S1 segment of hKv1.1 channelsImbrici, Paola; Cusimano, Antonella; D'Adamo, Maria Cristina; Curtis, Amalia de; Pessia, Mauro
2012Dysfunction of voltage-gated K + Channels Kv1.1 in sciatic nerve causes spontaneous and stress-induced neuromuscular hyperexcitabilityBrunetti, Orazio; Imbrici, Paola; Botti, Fabio Massimo; Pettorossi, Vito Enrico; D’Adamo, Maria Cristina; Valentino, Mario; Zammit, Christian; Mora, Marina; Di Giovanni, Giuseppe; Muscat, Richard; Pessia, Mauro
2023An activator of voltage-gated K+ channels Kv1.1 as a therapeutic candidate for episodic ataxia type 1Servettini, Ilenio; Talani, Giuseppe; Megaro, Alfredo; Setzu, Maria Dolores; Biggio, Francesca; Briffa, Michelle; Guglielmi, Luca; Savalli, Nicoletta; Binda, Francesca; Delicata, Francis; Bru–Mercier, Gilles; Vassallo, Neville; Maglione, Vittorio; Cauchi, Ruben J.; Di Pardo, Alba; Colluc, Maria; Imbrici, Paola; Catacuzzeno, Luigi; D’Adamo, Maria Cristina; Olcese, Riccardo; Pessia, Mauro
2020Electromechanical coupling of the Kv1.1 voltage-gated K+ channel is fine-tuned by the simplest amino acid residue in the S4-S5 linkerHasan, Sonia; Megaro, Alfredo; Cenciarini, Marta; Coretti, Lorena; Botti, Fabio Massimo; Imbrici, Paola; Steinbusch, Harry W. M.; Hunter, Therese; Hunter, Gary; Pessia, Mauro; D’Adamo, Maria Cristina
2018Commentary : a channelopathy mutation in the voltage-sensor discloses contributions of a conserved phenylalanine to gating properties of Kv1.1 channels and ataxiaHasan, Sonia; Hunter, Therese; Hunter, Gary; Pessia, Mauro; D'Adamo, Maria Cristina