Browsing by Author D'Adamo, Maria Cristina

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Issue DateTitleAuthor(s)
20135-HT2 receptors-mediated modulation of voltage-gated K+ channels and neurophysiopathological correlatesD'Adamo, Maria Cristina; Servettini, Ilenio; Guglielmi, Luca; Matteo, Vincenzo di; Maio, Roberto di; Di Giovanni, Giuseppe; Pessia, Mauro
2015Animal models of episodic ataxia type 1 (EA1)D'Adamo, Maria Cristina; Di Giovanni, Giuseppe; Pessia, Mauro
2011Autism with seizures and intellectual disability : possible causative role of gain-of-function of the inwardly-rectifying K + channel Kir4.1Sicca, Federico; Imbrici, Paola; D'Adamo, Maria Cristina; Moro, Francesca; Bonatti, Fabrizia; Brovedani, Paola; Grottesi, Alessandro; Guerrini, Renzo; Masi, Gabriele; Santorelli, Filippo Maria; Pessia, Mauro
2016A Calsequestrin-1 mutation associated with a skeletal muscle disease alters sarcoplasmic Ca2+ releaseD'Adamo, Maria Cristina; Sforna, Luigi; Visentin, Sergio; Grottesi, Alessandro; Servettini, Llenio; Guglielmi, Luca; Macchioni, Lara; Saredi, Simona; Curcio, Maurizio; Nuccio de, Chiara; Hasan, Sonia M.; Corazzi, L.; Franciolini, Fabio; Mora, Marina; Catacuzzeno, Luigi; Pessia, Mauro
1993Changes of the hemostatic balance in a model of aging in ratsCurtis, Amalia de; Iacoviello, Licia; D'Adamo, Maria Cristina; Donati, Maria Benedetta
2017A channelopathy mutation in the voltage-sensor discloses contributions of a conserved phenylalanine to gating properties of Kv1.1 channels and ataxiaHasan, Sonia M.; Bove, Cecilia; Silvestri, Gabriella; Mantuano, Elide; Modoni, Anna; Veneziano, Liana; Macchioni, Lara; Hunter, Therese; Hunter, Gary J.; Pessia, Mauro; D'Adamo, Maria Cristina
2009Contributions of the central hydrophobic residue in the PXP motif of voltage-dependent K+ channels to S6 flexibility and gating propertiesImbrici, Paola; Grottesi, Alessandro; D'Adamo, Maria Cristina; Tucker, Stephen J.; Pessia, Mauro
1992Different response of vascular fibrinolysis to adrenergic stimulation in young and aged ratsIacoviello, Licia; D'Adamo, Maria Cristina; Curtis, Amalia de; Donati, Maria Benedetta
2001Differential pH sensitivity of Kir4.1 and Kir4.2 potassium channels and their modulation by heteropolymerisation with Kir5.1Pessia, Mauro; Imbrici, Paola; D'Adamo, Maria Cristina; Salvatore, Lorena; Tucker, Stephen J.
1992Effect of aspirin on the fibrinolytic response in perfused rat hindquartersIacoviello, Licia; Curtis, Amalia de; Amore, Concetta; D'Adamo, Maria Cristina; Buczko, Wlodzimierz; Gaetano, Giovanni de; Donati, Maria Benedetta
2012Episodic ataxia type 1D'Adamo, Maria Cristina; Hanna, Michael G.; Di Giovanni, Giuseppe; Pessia, Mauro
2007Episodic ataxia type 1 mutation F184C alters Zn2+-induced modulation of the human K+ channel Kv1.4-Kv1.1/Kvβ1.1Imbrici, Paola; D'Adamo, Maria Cristina; Cusimano, Antonella; Pessia, Mauro
2011Episodic ataxia type 1 mutations affect fast inactivation of K + channels by a reduction in either subunit surface expression or affinity for inactivation domainImbrici, Paola; D'Adamo, Maria Cristina; Grottesi, Alessandro; Biscarini, Andrea; Pessia, Mauro
2006Episodic ataxia type 1 mutations in the KCNA1 gene impair the fast inactivation properties of the human potassium channels Kv1.4-1.1/Kvβ1.1 and Kv1.4-1.1/Kvβ1.2Imbrici, Paola; D'Adamo, Maria Cristina; Kullmann, Dimitri M.; Pessia, Mauro
2004An episodic ataxia type-1 mutation in the S1 segment sensitises the hKv1.1 potassium channel to extracellular Zn2+Cusimano, Antonella; D'Adamo, Maria Cristina; Pessia, Mauro
1998Episodic ataxia type-1 mutations in the hKv1.1 cytoplasmic pore region alter the gating properties of the channelD'Adamo, Maria Cristina; Liu, Zhaoping; Adelman, John P.; Maylie, James G.; Pessia, Mauro
2002Expression in E. coli and purification of recombinant fragments of wild type and mutant human prion proteinCorsaro, A.; Thellung, Stefano; Russo, Claudio; Villa, Valentina; Arena, Sara; D'Adamo, Maria Cristina; Paludi, Domenico; Rossi Principe, D.; Damonte, Gianluca L.; Benatti, Umberto; Aceto, Antonio; Tagliavini, Fabrizio; Schettini, Gennaro; Florio, Tullio
2007Functional characterisation of a novel mutation causing episodic ataxia type 1 occurring in the KCNA1 geneImbrici, Paola; Gualandi, Francesca; D'Adamo, Maria Cristina; Cudia, Paola; Grandis, Domenico de; Ferlini, Alessandra; Pessia, Mauro
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 de, Amalia; Pessia, Mauro
2016Gain-of-function defects of astrocytic Kir4.1 channels in children with autism spectrum disorders and epilepsySicca, Federico; Ambrosini, Elena; Marchese, Maria; Sforna, Luigi; Servettini, Ilenio; Valvo, Giulia; Brignone, Maria Stefania; Lanciotti, Angela; Moro, Francesca; Grottesi, Alessandro; Catacuzzeno, Luigi; Baldini, Sara; Hasan, Sonia M.; D'Adamo, Maria Cristina; Franciolini, Fabio; Molinari, Paola; Santorelli, Filippo Maria; Pessia, Mauro