Structure, Gating and Basic Functions of the Ca(2+)-activated K Channel of Intermediate Conductance

por Sforna, Luigi, Megaro, Alfredo, Pessia, Mauro, Franciolini, Fabio, Catacuzzeno, Luigi
Publicado 2018

Commentary: A channelopathy mutation in the voltage-sensor discloses contributions of a conserved phenylalanine to gating properties of Kv1.1 channels and ataxia

por Hasan, Sonia, Hunter, Therese, Hunter, Gary, Pessia, Mauro, D'Adamo, Maria Cristina
Publicado 2018

K(+) channelepsy: progress in the neurobiology of potassium channels and epilepsy

por D'Adamo, Maria Cristina, Catacuzzeno, Luigi, Di Giovanni, Giuseppe, Franciolini, Fabio, Pessia, Mauro
Publicado 2013

Erratum: K(+) channelepsy: progress in the neurobiology of potassium channels and epilepsy

por D'Adamo, Maria C., Catacuzzeno, Luigi, Di Giovanni, Giuseppe, Franciolini, Fabio, Pessia, Mauro
Publicado 2014

Kv1.1 Channelopathies: Pathophysiological Mechanisms and Therapeutic Approaches

por D’Adamo, Maria Cristina, Liantonio, Antonella, Rolland, Jean-Francois, Pessia, Mauro, Imbrici, Paola
Publicado 2020

ClC-1 chloride channels: state-of-the-art research and future challenges

por Imbrici, Paola, Altamura, Concetta, Pessia, Mauro, Mantegazza, Renato, Desaphy, Jean-François, Camerino, Diana Conte
Publicado 2015

The role of ion channels in the hypoxia-induced aggressiveness of glioblastoma

por Sforna, Luigi, Cenciarini, Marta, Belia, Silvia, D’Adamo, Maria Cristina, Pessia, Mauro, Franciolini, Fabio, Catacuzzeno, Luigi
Publicado 2015

Update on the implication of potassium channels in autism: K(+) channelautism spectrum disorder

por Guglielmi, Luca, Servettini, Ilenio, Caramia, Martino, Catacuzzeno, Luigi, Franciolini, Fabio, D’Adamo, Maria Cristina, Pessia, Mauro
Publicado 2015

Reconciling the discrepancies on the involvement of large-conductance Ca(2+)-activated K channels in glioblastoma cell migration

por Catacuzzeno, Luigi, Caramia, Martino, Sforna, Luigi, Belia, Silvia, Guglielmi, Luca, D’Adamo, Maria Cristina, Pessia, Mauro, Franciolini, Fabio
Publicado 2015

Dexamethasone in Glioblastoma Multiforme Therapy: Mechanisms and Controversies

por Cenciarini, Marta, Valentino, Mario, Belia, Silvia, Sforna, Luigi, Rosa, Paolo, Ronchetti, Simona, D’Adamo, Maria Cristina, Pessia, Mauro
Publicado 2019

Kcnj16 (Kir5.1) Gene Ablation Causes Subfertility and Increases the Prevalence of Morphologically Abnormal Spermatozoa

por Poli, Giulia, Hasan, Sonia, Belia, Silvia, Cenciarini, Marta, Tucker, Stephen J., Imbrici, Paola, Shehab, Safa, Pessia, Mauro, Brancorsini, Stefano, D’Adamo, Maria Cristina
Publicado 2021

Locus Coeruleus Neurons’ Firing Pattern Is Regulated by ERG Voltage-Gated K(+) Channels

por Hasan, Sonia, Delicata, Francis, Guasti, Leonardo, Duranti, Claudia, Haidar, Fatemah Mousalem, Arcangeli, Annarosa, Imbrici, Paola, Pessia, Mauro, Valentino, Mario, D’Adamo, Maria Cristina
Publicado 2022

A channelopathy mutation in the voltage-sensor discloses contributions of a conserved phenylalanine to gating properties of Kv1.1 channels and ataxia

por Hasan, Sonia, Bove, Cecilia, Silvestri, Gabriella, Mantuano, Elide, Modoni, Anna, Veneziano, Liana, Macchioni, Lara, Hunter, Therese, Hunter, Gary, Pessia, Mauro, D’Adamo, Maria Cristina
Publicado 2017

Identification of a New de Novo Mutation Underlying Regressive Episodic Ataxia Type I

por Karalok, Zeynep S., Megaro, Alfredo, Cenciarini, Marta, Guven, Alev, Hasan, Sonia M., Taskin, Birce D., Imbrici, Paola, Ceylaner, Serdar, Pessia, Mauro, D'Adamo, Maria C.
Publicado 2018

Association of A Novel Splice Site Mutation in P/Q-Type Calcium Channels with Childhood Epilepsy and Late-Onset Slowly Progressive Non-Episodic Cerebellar Ataxia

por Stendel, Claudia, D’Adamo, Maria Cristina, Wiessner, Manuela, Dusl, Marina, Cenciarini, Marta, Belia, Silvia, Nematian-Ardestani, Ehsan, Bauer, Peter, Senderek, Jan, Klopstock, Thomas, Pessia, Mauro
Publicado 2020

Kv1.1 knock-in ataxic mice exhibit spontaneous myokymic activity exacerbated by fatigue, ischemia and low temperature

por Brunetti, Orazio, Imbrici, Paola, Botti, Fabio Massimo, Pettorossi, Vito Enrico, D'Adamo, Maria Cristina, Valentino, Mario, Zammit, Christian, Mora, Marina, Gibertini, Sara, Di Giovanni, Giuseppe, Muscat, Richard, Pessia, Mauro
Publicado 2012

KCNK18 Biallelic Variants Associated with Intellectual Disability and Neurodevelopmental Disorders Alter TRESK Channel Activity

por Pavinato, Lisa, Nematian-Ardestani, Ehsan, Zonta, Andrea, De Rubeis, Silvia, Buxbaum, Joseph, Mancini, Cecilia, Bruselles, Alessandro, Tartaglia, Marco, Pessia, Mauro, Tucker, Stephen J., D’Adamo, Maria Cristina, Brusco, Alfredo
Publicado 2021

A Calsequestrin-1 Mutation Associated with a Skeletal Muscle Disease Alters Sarcoplasmic Ca(2+) Release

por 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
Publicado 2016

Novel phenotype associated with a mutation in the KCNA1(Kv1.1) gene

por D'Adamo, Maria C., Gallenmüller, Constanze, Servettini, Ilenio, Hartl, Elisabeth, Tucker, Stephen J., Arning, Larissa, Biskup, Saskia, Grottesi, Alessandro, Guglielmi, Luca, Imbrici, Paola, Bernasconi, Pia, Di Giovanni, Giuseppe, Franciolini, Fabio, Catacuzzeno, Luigi, Pessia, Mauro, Klopstock, Thomas
Publicado 2015

The CaMKII/MLC1 Axis Confers Ca(2+)-Dependence to Volume-Regulated Anion Channels (VRAC) in Astrocytes

por Brignone, Maria Stefania, Lanciotti, Angela, Michelucci, Antonio, Mallozzi, Cinzia, Camerini, Serena, Catacuzzeno, Luigi, Sforna, Luigi, Caramia, Martino, D’Adamo, Maria Cristina, Ceccarini, Marina, Molinari, Paola, Macioce, Pompeo, Macchia, Gianfranco, Petrucci, Tamara Corinna, Pessia, Mauro, Visentin, Sergio, Ambrosini, Elena
Publicado 2022