PESSIA, Mauro
PESSIA, Mauro
DIPARTIMENTO DI MEDICINA SPERIMENTALE (attivo dal 01/01/2014 al 31/10/2020)
5-HT2 receptors-mediated modulation of voltage-gated K+ channels and neurophysiopathological correlates
2013 D'Adamo, Maria Cristina; Servettini, Ilenio; Luca, Guglielmi; Vincenzo Di, Matteo; Roberto Di, Maio; Giuseppe Di, Giovanni; Pessia, Mauro
A Calsequestrin-1 mutation associated with a skeletal muscle disease alters sarcoplasmic Ca2+ release
2016 D'Adamo, Maria Cristina; Sforna, Luigi; Visentin, Sergio; Grottesi, Alessandro; Servettini, Llenio; Guglielmi, Luca; Macchioni, Lara; Saredi, Simona; Curcio, Maurizio; De Nuccio, Chiara; Hasan, Sonia; Corazzi, Lanfranco; Franciolini, Fabio; Mora, Marina; Catacuzzeno, Luigi; Pessia, Mauro
A CASQ1 founder mutation in three Italian families with protein aggregate myopathy and hyperCKaemia
2015 Di Blasi, Claudia; Sansanelli, Serena; Ruggieri, Alessandra; Moriggi, Manuela; Vasso, Michele; D'Adamo, Adamo Pio; Blasevich, Flavia; Zanotti, Simona; Paolini, Cecilia; Protasi, Feliciano; Tezzon, Frediano; Gelfi, Cecilia; Morandi, Lucia; Pessia, Mauro; Mora, Marina
A channelopathy mutation in the voltage-sensor discloses contributions of a conserved phenylalanine to gating properties of Kv1.1 channels and ataxia
2017 Hasan, Sonia; Bove, Cecilia; Silvestri, Gabriella; Mantuano, Elide; Modoni, Anna; Veneziano, Liana; Macchioni, Lara; Hunter, Therese; Hunter, Gary; Pessia, Mauro; D'Adamo, Maria Cristina
A large cohort of myotonia congenita probands: novel mutations and a high-frequency mutation region in exons 4 and 5 of the CLCN1 gene.
2013 Brugnoni, R.; Kapetis, D.; Imbrici, Paola; Pessia, Mauro; Canioni, E.; Colleoni, L.; de Rosbo, N. K.; Morandi, L.; Cudia, P.; Gashemi, N.; Bernasconi, P.; Desaphy, J. F.; Conte, D.; Mantegazza, R.
A method to identify tissue cell subpopulations with distinct multi-molecular profiles from data on co-localization of two markers at a time: the case of sensory ganglia
2014 Catacuzzeno, Luigi; Sforna, Luigi; D'Adamo, Maria Cristina; Pessia, Mauro; Franciolini, Fabio
A Novel KCNA1 Mutation Identified in an Italian Family Affected by Episodic Ataxia Type 1
2008 Imbrici, Paola; Gualandi, F; D'Adamo, Maria Cristina; TADDEI MASIERI, M; Cudia, P; DE GRANDIS, D; Mannucci, R; Nicoletti, Ildo; Tucker, Sj; Ferlini, A; Pessia, Mauro
A novel KCNA1 mutation in a patient with paroxysmal ataxia, myokymia, painful contractures and metabolic dysfunctions
2017 Imbrici, Paola; Altamura, Concetta; Gualandi, Francesca; Mangiatordi, Giuseppe Felice; Neri, Marcella; De Maria, Giovanni; Ferlini, Alessandra; Padovani, Alessandro; D'Adamo, Maria Cristina; Nicolotti, Orazio; Pessia, Mauro; Conte, Diana; Filosto, Massimiliano; Desaphy, Jean-Francois
Actions of 5-hydroxytryptamine on ventral tegmental area neurons of the rat in vitro.
1994 Pessia, Mauro; Jiang, Z. G.; North, R. A.; Johnson, S. W.
All atom molecular dynamics simulation of the K+ Channel Chimera Kv1.2/2.1
2010 Grottesi, A.; Imbrici, Paola; Chillemi, G.; Pessia, Mauro
An activator of voltage-gated K + channels Kv1.1 as a therapeutic candidate for episodic ataxia type 1
2023 Servettini, 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; Collu, Maria; Imbrici, Paola; Catacuzzeno, Luigi; D’Adamo, Maria Cristina; Olcese, Riccardo; Pessia, Mauro
An Episodic Ataxia Type-1 (EA1) mutation in the S1 segment sensitises the hKv1.1 potassium channel to extracellular Zn2+
2004 Cusimano, A.; D'Adamo, Maria Cristina; Pessia, Mauro
Animal Models of Episodic Ataxia Type 1 (EA1).
2014 D'Adamo, Maria Cristina; Di Giovanni, G.; Pessia, Mauro
Author Correction: Thymosin α1 represents a potential potent single-molecule-based therapy for cystic fibrosis
2018 Romani, Luigina; Oikonomou, Vasilis; Moretti, Silvia; Iannitti, Rossana G; D'Adamo, Maria Cristina; Villella, Valeria R; Pariano, Marilena; Sforna, Luigi; Borghi, Monica; Bellet, Marina M; Fallarino, Francesca; Pallotta, Maria Teresa; Servillo, Giuseppe; Ferrari, Eleonora; Puccetti, Paolo; Kroemer, Guido; Pessia, Mauro; Maiuri, Luigi; Goldstein, Allan L; Garaci, Enrico
Autism with Seizures and Intellectual Disability: Possible Causative Role of Gain-of-Function of the Inwardly-Rectifying K+ Channel Kir4.1.
2011 Sicca, F.; Imbrici, Paola; D'Adamo, Maria Cristina; Moro, F.; Bonatti, F.; Brovedani, P; Grottesi, A.; Guerrini, R.; Masi, G.; Santorelli, F. M.; Pessia, Mauro
CIC-1 chloride channels: State-of-the-art research and future challenges
2015 Imbrici, Paola; Altamura, Concetta; Pessia, Mauro; Mantegazza, Renato; Desaphy, Jean François; Camerino, Diana Conte
Cloning and expression of a family of inward rectifier potassium channels.
1994 Bond, C. T.; Pessia, Mauro; Xia, X. M.; Lagrutta, A.; Kavanaugh, M. P.; Adelman, J. P.
Commentary: A channelopathy mutation in the voltage-sensor discloses contributions of a conserved phenylalanine to gating properties of Kv1.1 channels and ataxia
2018 Hasan, Sonia; Hunter, Therese; Hunter, Gary; Pessia, Mauro; D'Adamo, Maria Cristina
Contributions of the C-terminal domain to gating properties of inward rectifier potassium channels.
1995 Pessia, Mauro; Bond, C. T.; Kavanaugh, M. P.; Adelman, J. P.
Contributions of the central hydrophobic residue in the PXP motif of Voltage-Dependent K+ Channels to S6 flexibility and Gating Properties
2009 Imbrici, P; Grottesi, A; D'Adamo, Maria Cristina; Mannucci, R; Tucker, Sj; Pessia, Mauro
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| 5-HT2 receptors-mediated modulation of voltage-gated K+ channels and neurophysiopathological correlates | 2013 | D'Adamo, Maria Cristina; Servettini, Ilenio; Luca, Guglielmi; Vincenzo Di, Matteo; Roberto Di, Maio; Giuseppe Di, Giovanni; Pessia, Mauro | |
| A Calsequestrin-1 mutation associated with a skeletal muscle disease alters sarcoplasmic Ca2+ release | 2016 | D'Adamo, Maria Cristina; Sforna, Luigi; Visentin, Sergio; Grottesi, Alessandro; Servettini, Llenio; Guglielmi, Luca; Macchioni, Lara; Saredi, Simona; Curcio, Maurizio; De Nuccio, Chiara; Hasan, Sonia; Corazzi, Lanfranco; Franciolini, Fabio; Mora, Marina; Catacuzzeno, Luigi; Pessia, Mauro | |
| A CASQ1 founder mutation in three Italian families with protein aggregate myopathy and hyperCKaemia | 2015 | Di Blasi, Claudia; Sansanelli, Serena; Ruggieri, Alessandra; Moriggi, Manuela; Vasso, Michele; D'Adamo, Adamo Pio; Blasevich, Flavia; Zanotti, Simona; Paolini, Cecilia; Protasi, Feliciano; Tezzon, Frediano; Gelfi, Cecilia; Morandi, Lucia; Pessia, Mauro; Mora, Marina | |
| A channelopathy mutation in the voltage-sensor discloses contributions of a conserved phenylalanine to gating properties of Kv1.1 channels and ataxia | 2017 | Hasan, Sonia; Bove, Cecilia; Silvestri, Gabriella; Mantuano, Elide; Modoni, Anna; Veneziano, Liana; Macchioni, Lara; Hunter, Therese; Hunter, Gary; Pessia, Mauro; D'Adamo, Maria Cristina | |
| A large cohort of myotonia congenita probands: novel mutations and a high-frequency mutation region in exons 4 and 5 of the CLCN1 gene. | 2013 | Brugnoni, R.; Kapetis, D.; Imbrici, Paola; Pessia, Mauro; Canioni, E.; Colleoni, L.; de Rosbo, N. K.; Morandi, L.; Cudia, P.; Gashemi, N.; Bernasconi, P.; Desaphy, J. F.; Conte, D.; Mantegazza, R. | |
| A method to identify tissue cell subpopulations with distinct multi-molecular profiles from data on co-localization of two markers at a time: the case of sensory ganglia | 2014 | Catacuzzeno, Luigi; Sforna, Luigi; D'Adamo, Maria Cristina; Pessia, Mauro; Franciolini, Fabio | |
| A Novel KCNA1 Mutation Identified in an Italian Family Affected by Episodic Ataxia Type 1 | 2008 | Imbrici, Paola; Gualandi, F; D'Adamo, Maria Cristina; TADDEI MASIERI, M; Cudia, P; DE GRANDIS, D; Mannucci, R; Nicoletti, Ildo; Tucker, Sj; Ferlini, A; Pessia, Mauro | |
| A novel KCNA1 mutation in a patient with paroxysmal ataxia, myokymia, painful contractures and metabolic dysfunctions | 2017 | Imbrici, Paola; Altamura, Concetta; Gualandi, Francesca; Mangiatordi, Giuseppe Felice; Neri, Marcella; De Maria, Giovanni; Ferlini, Alessandra; Padovani, Alessandro; D'Adamo, Maria Cristina; Nicolotti, Orazio; Pessia, Mauro; Conte, Diana; Filosto, Massimiliano; Desaphy, Jean-Francois | |
| Actions of 5-hydroxytryptamine on ventral tegmental area neurons of the rat in vitro. | 1994 | Pessia, Mauro; Jiang, Z. G.; North, R. A.; Johnson, S. W. | |
| All atom molecular dynamics simulation of the K+ Channel Chimera Kv1.2/2.1 | 2010 | Grottesi, A.; Imbrici, Paola; Chillemi, G.; Pessia, Mauro | |
| An activator of voltage-gated K + channels Kv1.1 as a therapeutic candidate for episodic ataxia type 1 | 2023 | Servettini, 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; Collu, Maria; Imbrici, Paola; Catacuzzeno, Luigi; D’Adamo, Maria Cristina; Olcese, Riccardo; Pessia, Mauro | |
| An Episodic Ataxia Type-1 (EA1) mutation in the S1 segment sensitises the hKv1.1 potassium channel to extracellular Zn2+ | 2004 | Cusimano, A.; D'Adamo, Maria Cristina; Pessia, Mauro | |
| Animal Models of Episodic Ataxia Type 1 (EA1). | 2014 | D'Adamo, Maria Cristina; Di Giovanni, G.; Pessia, Mauro | |
| Author Correction: Thymosin α1 represents a potential potent single-molecule-based therapy for cystic fibrosis | 2018 | Romani, Luigina; Oikonomou, Vasilis; Moretti, Silvia; Iannitti, Rossana G; D'Adamo, Maria Cristina; Villella, Valeria R; Pariano, Marilena; Sforna, Luigi; Borghi, Monica; Bellet, Marina M; Fallarino, Francesca; Pallotta, Maria Teresa; Servillo, Giuseppe; Ferrari, Eleonora; Puccetti, Paolo; Kroemer, Guido; Pessia, Mauro; Maiuri, Luigi; Goldstein, Allan L; Garaci, Enrico | |
| Autism with Seizures and Intellectual Disability: Possible Causative Role of Gain-of-Function of the Inwardly-Rectifying K+ Channel Kir4.1. | 2011 | Sicca, F.; Imbrici, Paola; D'Adamo, Maria Cristina; Moro, F.; Bonatti, F.; Brovedani, P; Grottesi, A.; Guerrini, R.; Masi, G.; Santorelli, F. M.; Pessia, Mauro | |
| CIC-1 chloride channels: State-of-the-art research and future challenges | 2015 | Imbrici, Paola; Altamura, Concetta; Pessia, Mauro; Mantegazza, Renato; Desaphy, Jean François; Camerino, Diana Conte | |
| Cloning and expression of a family of inward rectifier potassium channels. | 1994 | Bond, C. T.; Pessia, Mauro; Xia, X. M.; Lagrutta, A.; Kavanaugh, M. P.; Adelman, J. P. | |
| Commentary: A channelopathy mutation in the voltage-sensor discloses contributions of a conserved phenylalanine to gating properties of Kv1.1 channels and ataxia | 2018 | Hasan, Sonia; Hunter, Therese; Hunter, Gary; Pessia, Mauro; D'Adamo, Maria Cristina | |
| Contributions of the C-terminal domain to gating properties of inward rectifier potassium channels. | 1995 | Pessia, Mauro; Bond, C. T.; Kavanaugh, M. P.; Adelman, J. P. | |
| Contributions of the central hydrophobic residue in the PXP motif of Voltage-Dependent K+ Channels to S6 flexibility and Gating Properties | 2009 | Imbrici, P; Grottesi, A; D'Adamo, Maria Cristina; Mannucci, R; Tucker, Sj; Pessia, Mauro |