Sfoglia per Autore
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
Mutations in KCNA1 affect stoichiometry and fast inactivation of heteromeric K+ channels
2009 Imbrici, Paola; D'Adamo, Maria Cristina; Maylie, J.; Pessia, Mauro
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
All atom molecular dynamics simulation of the K+ Channel Chimera Kv1.2/2.1
2010 Grottesi, A.; Imbrici, Paola; Chillemi, G.; Pessia, Mauro
Trace amines depress D2-autoreceptor-mediated responses on midbrain dopaminergic cells.
2010 Ledonne, A; Federici, M; Giustizieri, M; Pessia, Mauro; Imbrici, Paola; Millan, Mj; Bernardi, G; Mercuri, Nb
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
The emerging role of the inwardly rectifying K+channels in autism spectrum disorders andepilepsy
2011 D'Adamo, Maria Cristina; Moro, F.; Imbrici, Paola; Martino, D.; Roscini, Mauro; Santorelli, F. M.; Sicca, F.; Pessia, Mauro
The Kir5.1 Potassium Channel is an Important Determinant of Neuronal PCO2/pH Sensitivity
2011 D'Adamo, Maria Cristina; Shang, L.; Imbrici, Paola; Brown, S. D. M.; Pessia, Mauro; Tucker, S. J.
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
Genetic inactivation of Kcnj16 identifies Kir5.1 as an important determinant of neuronal PCO2/pH sensitivity
2011 D'Adamo, Maria Cristina; Shang, L; Imbrici, Paola; Brown, Sdm; Pessia, Mauro; Tucker, S.
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
The neurobiology of episodic ataxia type 1: a Shaker-like K+ channel disorder.
2012 Pessia, Mauro; D'Adamo, Maria Cristina; Imbrici, Paola
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.
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
Identification of a New de Novo Mutation Underlying Regressive Episodic Ataxia Type I
2018 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.
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.
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
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| 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 | |
| Mutations in KCNA1 affect stoichiometry and fast inactivation of heteromeric K+ channels | 2009 | Imbrici, Paola; D'Adamo, Maria Cristina; Maylie, J.; Pessia, Mauro | |
| 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 | |
| All atom molecular dynamics simulation of the K+ Channel Chimera Kv1.2/2.1 | 2010 | Grottesi, A.; Imbrici, Paola; Chillemi, G.; Pessia, Mauro | |
| Trace amines depress D2-autoreceptor-mediated responses on midbrain dopaminergic cells. | 2010 | Ledonne, A; Federici, M; Giustizieri, M; Pessia, Mauro; Imbrici, Paola; Millan, Mj; Bernardi, G; Mercuri, Nb | |
| 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 | |
| The emerging role of the inwardly rectifying K+channels in autism spectrum disorders andepilepsy | 2011 | D'Adamo, Maria Cristina; Moro, F.; Imbrici, Paola; Martino, D.; Roscini, Mauro; Santorelli, F. M.; Sicca, F.; Pessia, Mauro | |
| The Kir5.1 Potassium Channel is an Important Determinant of Neuronal PCO2/pH Sensitivity | 2011 | D'Adamo, Maria Cristina; Shang, L.; Imbrici, Paola; Brown, S. D. M.; Pessia, Mauro; Tucker, S. J. | |
| 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 | |
| Genetic inactivation of Kcnj16 identifies Kir5.1 as an important determinant of neuronal PCO2/pH sensitivity | 2011 | D'Adamo, Maria Cristina; Shang, L; Imbrici, Paola; Brown, Sdm; Pessia, Mauro; Tucker, S. | |
| 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 | |
| The neurobiology of episodic ataxia type 1: a Shaker-like K+ channel disorder. | 2012 | Pessia, Mauro; D'Adamo, Maria Cristina; Imbrici, Paola | |
| 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. | |
| 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 | |
| Identification of a New de Novo Mutation Underlying Regressive Episodic Ataxia Type I | 2018 | 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. | |
| 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. | |
| 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 |
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