IMBRICI, Paola
IMBRICI, Paola
DIPARTIMENTO DI MEDICINA INTERNA (attivo dal 14/09/1994 al 31/12/2013)
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 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
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
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
Contributions of the central hydrophobic residue in the PXP motif of Voltage-Dependent K+ Channels to S6 flexibility and Gating Properties.
2009 Imbrici, Paola; A., Grottesi; D'Adamo, Maria Cristina; S. J., Tucker; Pessia, Mauro
Copertina della rivista The Journal of Physiology
2001 Pessia, Mauro; Imbrici, Paola; D'Adamo, Maria Cristina; Salvatore, L.; Tucker, S. J.
Differential pH-sensitivity of Kir4.1 and Kir4.2 and modulation by heteropolymerisation with Kir5.1
2001 Pessia, Mauro; Imbrici, Paola; D'Adamo, Maria Cristina; Salvatore, L.; Tucker, S. J.
EA-1 mutations alter the fast inactivation properties of Kv1.1 channels conferred by Kv1.4 and Kvbeta1.1 subunits
2005 Pessia, Mauro; Imbrici, Paola; D’Adamo, M.
Effects of Episodic Ataxia-Associated Mutations on hKv1.4-1.1/Kvbeta1 channels
2005 D'Adamo, Maria Cristina; Imbrici, Paola; Servettini, Ilenio; Picconi, B.; Pessia, Mauro
Electromechanical coupling of the Kv1.1 voltage-gated K+ channel is fine-tuned by the simplest amino acid residue in the S4-S5 linker
2020 Hasan, S; Megaro, A; Cenciarini, M; Coretti, L; Botti, F. M.; Imbrici, P; Steinbusch, H. W. M.; Hunter, T; Hunter, G; Pessia, M.; D’Adamo, M. C.
Episodic Ataxia Type 1 Mutation F184C Alters Zn2+-Induced Modulation of the Human Potassium Channel Kv1.4-Kv1.1/Kvbeta1.1
2007 Imbrici, Paola; D'Adamo, Maria Cristina; Cusimano, A; Pessia, Mauro
Episodic Ataxia Type 1 Mutations Affect Fast Inactivation of K+ Channels by a Reduction in Either Subunit Surface Expression or Affinity for Inactivation Domain
2011 Imbrici, Paola; D'Adamo, Maria Cristina; Grottesi, A.; Biscarini, Andrea; Pessia, Mauro
Episodic ataxia type 1 mutations cause loss-of-function impairments of heteromeric channels formed by the Kv1.4 and Kv1.1 subunits.
2007 Imbrici, Paola; D'Adamo, Maria Cristina; Servettini, Ilenio; Pessia, Mauro
Episodic Ataxia Type 1 Mutations in the KCNA1 Gene Impair the Fast Inactivation Properties of the Human K+ Channels Kv1.4-1.1/Kvbeta1.1 and Kv1.4-1.1/Kvbeta1.2.
2006 Imbrici, Paola; D'Adamo, Maria Cristina; Kullmann, D. M.; Pessia, Mauro
Episodic Ataxias as Ion Channel Diseases.
2002 D'Adamo, Maria Cristina; Imbrici, Paola; Pessia, Mauro
Functional Characterization of an Episodic Ataxia Type-1 Mutation Occurring in the S1 Segment of hKv1.1 Channels.
2003 Imbrici, Paola; Cusimano, A.; D'Adamo, Maria Cristina; Pessia, Mauro
Functional Properties of Voltage-Gated Potassium Channels Probed with Methanethiosulfonate Reagents.
2001 Cusimano, A.; Imbrici, Paola; D'Adamo, Maria Cristina; Pessia, Mauro
Gain-of-Function of the Inwardly-Rectifying K+ Channel Kir4.1 Contributes to Autism with Seizures and Intellectual Disability.
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
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| 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 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 | |
| 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 | |
| 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 | |
| Contributions of the central hydrophobic residue in the PXP motif of Voltage-Dependent K+ Channels to S6 flexibility and Gating Properties. | 2009 | Imbrici, Paola; A., Grottesi; D'Adamo, Maria Cristina; S. J., Tucker; Pessia, Mauro | |
| Copertina della rivista The Journal of Physiology | 2001 | Pessia, Mauro; Imbrici, Paola; D'Adamo, Maria Cristina; Salvatore, L.; Tucker, S. J. | |
| Differential pH-sensitivity of Kir4.1 and Kir4.2 and modulation by heteropolymerisation with Kir5.1 | 2001 | Pessia, Mauro; Imbrici, Paola; D'Adamo, Maria Cristina; Salvatore, L.; Tucker, S. J. | |
| EA-1 mutations alter the fast inactivation properties of Kv1.1 channels conferred by Kv1.4 and Kvbeta1.1 subunits | 2005 | Pessia, Mauro; Imbrici, Paola; D’Adamo, M. | |
| Effects of Episodic Ataxia-Associated Mutations on hKv1.4-1.1/Kvbeta1 channels | 2005 | D'Adamo, Maria Cristina; Imbrici, Paola; Servettini, Ilenio; Picconi, B.; Pessia, Mauro | |
| Electromechanical coupling of the Kv1.1 voltage-gated K+ channel is fine-tuned by the simplest amino acid residue in the S4-S5 linker | 2020 | Hasan, S; Megaro, A; Cenciarini, M; Coretti, L; Botti, F. M.; Imbrici, P; Steinbusch, H. W. M.; Hunter, T; Hunter, G; Pessia, M.; D’Adamo, M. C. | |
| Episodic Ataxia Type 1 Mutation F184C Alters Zn2+-Induced Modulation of the Human Potassium Channel Kv1.4-Kv1.1/Kvbeta1.1 | 2007 | Imbrici, Paola; D'Adamo, Maria Cristina; Cusimano, A; Pessia, Mauro | |
| Episodic Ataxia Type 1 Mutations Affect Fast Inactivation of K+ Channels by a Reduction in Either Subunit Surface Expression or Affinity for Inactivation Domain | 2011 | Imbrici, Paola; D'Adamo, Maria Cristina; Grottesi, A.; Biscarini, Andrea; Pessia, Mauro | |
| Episodic ataxia type 1 mutations cause loss-of-function impairments of heteromeric channels formed by the Kv1.4 and Kv1.1 subunits. | 2007 | Imbrici, Paola; D'Adamo, Maria Cristina; Servettini, Ilenio; Pessia, Mauro | |
| Episodic Ataxia Type 1 Mutations in the KCNA1 Gene Impair the Fast Inactivation Properties of the Human K+ Channels Kv1.4-1.1/Kvbeta1.1 and Kv1.4-1.1/Kvbeta1.2. | 2006 | Imbrici, Paola; D'Adamo, Maria Cristina; Kullmann, D. M.; Pessia, Mauro | |
| Episodic Ataxias as Ion Channel Diseases. | 2002 | D'Adamo, Maria Cristina; Imbrici, Paola; Pessia, Mauro | |
| Functional Characterization of an Episodic Ataxia Type-1 Mutation Occurring in the S1 Segment of hKv1.1 Channels. | 2003 | Imbrici, Paola; Cusimano, A.; D'Adamo, Maria Cristina; Pessia, Mauro | |
| Functional Properties of Voltage-Gated Potassium Channels Probed with Methanethiosulfonate Reagents. | 2001 | Cusimano, A.; Imbrici, Paola; D'Adamo, Maria Cristina; Pessia, Mauro | |
| Gain-of-Function of the Inwardly-Rectifying K+ Channel Kir4.1 Contributes to Autism with Seizures and Intellectual Disability. | 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 |