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109. Involvement of the Na+-H+ antiporter on the effect of protein kinase-C activation on dopamine synthesis in rat corpus striatum
1988-01-01 Amoroso, S; Annunziato, L; Taglialatela, Maurizio; Di Renzo, Gf; Canzoniero, Lm; Galizia, G; Marino, A.
A novel homozygous KCNQ3 loss-of-function variant causes non-syndromic intellectual disability and neonatal-onset pharmacodependent epilepsy
2019-01-01 Lauritano, A.; Moutton, S.; Longobardi, E.; Tran Mau-Them, F.; Laudati, G.; Nappi, P.; Soldovieri, M. V.; Ambrosino, P.; Cataldi, M.; Jouan, T.; Lehalle, D.; Maurey, H.; Philippe, C.; Miceli, F.; Vitobello, A.; Taglialatela, M.
A novel hyperekplexia-causing mutation in the pre-transmembrane segment 1 of the human glycine receptor alpha(1) subunit reduces membrane expression and impairs gating by agonists
2004-01-01 Castaldo, P; Stefanoni, P; Miceli, F; Coppola, G; del Giudice, Em; Bellini, G; Pascotto, A; Trudell, Jr; Harrison, Nl; Annunziato, L; Taglialatela, Maurizio
A novel KCNC1 gain-of-function variant causing developmental and epileptic encephalopathy: "Precision medicine" approach with fluoxetine
2023-01-01 Ambrosino, Paolo; Ragona, Francesca; Mosca, Ilaria; Vannicola, Chiara; Canafoglia, Laura; Solazzi, Roberta; Rivolta, Ilaria; Freri, Elena; Granata, Tiziana; Messina, Giuliana; Castellotti, Barbara; Gellera, Cinzia; Soldovieri, Maria Virginia; Difrancesco, Jacopo Cosimo; Taglialatela, Maurizio
A novel KCNQ2 K+ channel mutation in benign neonatal convulsions and centrotemporal spikes
2003-01-01 Coppola, G; Castaldo, P; del Giudice, Em; Bellini, G; Galasso, F; Soldovieri, Maria Virginia; Anzalone, L; Sferro, C; Annuniziato, L; Taglialatela, Maurizio
A novel KCNQ3 mutation in familial epilepsy with focal seizures and intellectual disability.
2015-01-01 Miceli, F; Striano, P; Soldovieri, Maria Virginia; Fontana, A; Nardello, R; Robbiano, A; Bellini, G; Elia, M; Zara, F; Taglialatela, Maurizio; Mangano, S.
A Novel Kv7.3 Variant in the Voltage-Sensing S4 Segment in a Family With Benign Neonatal Epilepsy: Functional Characterization and in vitro Rescue by β-Hydroxybutyrate
2020-01-01 Miceli, F.; Carotenuto, L.; Barrese, V.; Soldovieri, M. V.; Heinzen, E. L.; Mandel, A. M.; Lippa, N.; Bier, L.; Goldstein, D. B.; Cooper, E. C.; Cilio, M. R.; Taglialatela, M.; Sands, T. T.
A novel mutation in KCNQ2 associated with BFNC, drug resistant epilepsy, and mental retardation
2004-01-01 Borgatti, R; Zucca, C; Cavallini, A; Ferrario, M; Panzeri, C; Castaldo, P; Soldovieri, Maria Virginia; Baschirotto, C; Bresolin, N; Dalla Bernardina, B; Taglialatela, Maurizio; Bassi, Mt
A SINGLE NONPOLAR RESIDUE IN THE DEEP PORE OF RELATED K+ CHANNELS ACTS AS A K+-RB+ CONDUCTANCE SWITCH
1992-01-01 Kirsch, Ge; Drewe, Ja; Taglialatela, Maurizio; Joho, Rh; Debiasi, M; Hartmann, Ha; Brown, Am
A y(+)LAT-1 mutant protein interferes with y(+)LAT-2 activity: implications for the molecular pathogenesis of lysinuric protein intolerance
2005-01-01 Sperandeo, Mp; Paladino, S; Maiuri, L; Maroupulos, Gd; Zurzolo, C; Taglialatela, Maurizio; Andria, G; Sebastio, G.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| 109. Involvement of the Na+-H+ antiporter on the effect of protein kinase-C activation on dopamine synthesis in rat corpus striatum | 1-gen-1988 | Amoroso, S; Annunziato, L; Taglialatela, Maurizio; Di Renzo, Gf; Canzoniero, Lm; Galizia, G; Marino, A. | |
| A novel homozygous KCNQ3 loss-of-function variant causes non-syndromic intellectual disability and neonatal-onset pharmacodependent epilepsy | 1-gen-2019 | Lauritano, A.; Moutton, S.; Longobardi, E.; Tran Mau-Them, F.; Laudati, G.; Nappi, P.; Soldovieri, M. V.; Ambrosino, P.; Cataldi, M.; Jouan, T.; Lehalle, D.; Maurey, H.; Philippe, C.; Miceli, F.; Vitobello, A.; Taglialatela, M. | |
| A novel hyperekplexia-causing mutation in the pre-transmembrane segment 1 of the human glycine receptor alpha(1) subunit reduces membrane expression and impairs gating by agonists | 1-gen-2004 | Castaldo, P; Stefanoni, P; Miceli, F; Coppola, G; del Giudice, Em; Bellini, G; Pascotto, A; Trudell, Jr; Harrison, Nl; Annunziato, L; Taglialatela, Maurizio | |
| A novel KCNC1 gain-of-function variant causing developmental and epileptic encephalopathy: "Precision medicine" approach with fluoxetine | 1-gen-2023 | Ambrosino, Paolo; Ragona, Francesca; Mosca, Ilaria; Vannicola, Chiara; Canafoglia, Laura; Solazzi, Roberta; Rivolta, Ilaria; Freri, Elena; Granata, Tiziana; Messina, Giuliana; Castellotti, Barbara; Gellera, Cinzia; Soldovieri, Maria Virginia; Difrancesco, Jacopo Cosimo; Taglialatela, Maurizio | |
| A novel KCNQ2 K+ channel mutation in benign neonatal convulsions and centrotemporal spikes | 1-gen-2003 | Coppola, G; Castaldo, P; del Giudice, Em; Bellini, G; Galasso, F; Soldovieri, Maria Virginia; Anzalone, L; Sferro, C; Annuniziato, L; Taglialatela, Maurizio | |
| A novel KCNQ3 mutation in familial epilepsy with focal seizures and intellectual disability. | 1-gen-2015 | Miceli, F; Striano, P; Soldovieri, Maria Virginia; Fontana, A; Nardello, R; Robbiano, A; Bellini, G; Elia, M; Zara, F; Taglialatela, Maurizio; Mangano, S. | |
| A Novel Kv7.3 Variant in the Voltage-Sensing S4 Segment in a Family With Benign Neonatal Epilepsy: Functional Characterization and in vitro Rescue by β-Hydroxybutyrate | 1-gen-2020 | Miceli, F.; Carotenuto, L.; Barrese, V.; Soldovieri, M. V.; Heinzen, E. L.; Mandel, A. M.; Lippa, N.; Bier, L.; Goldstein, D. B.; Cooper, E. C.; Cilio, M. R.; Taglialatela, M.; Sands, T. T. | |
| A novel mutation in KCNQ2 associated with BFNC, drug resistant epilepsy, and mental retardation | 1-gen-2004 | Borgatti, R; Zucca, C; Cavallini, A; Ferrario, M; Panzeri, C; Castaldo, P; Soldovieri, Maria Virginia; Baschirotto, C; Bresolin, N; Dalla Bernardina, B; Taglialatela, Maurizio; Bassi, Mt | |
| A SINGLE NONPOLAR RESIDUE IN THE DEEP PORE OF RELATED K+ CHANNELS ACTS AS A K+-RB+ CONDUCTANCE SWITCH | 1-gen-1992 | Kirsch, Ge; Drewe, Ja; Taglialatela, Maurizio; Joho, Rh; Debiasi, M; Hartmann, Ha; Brown, Am | |
| A y(+)LAT-1 mutant protein interferes with y(+)LAT-2 activity: implications for the molecular pathogenesis of lysinuric protein intolerance | 1-gen-2005 | Sperandeo, Mp; Paladino, S; Maiuri, L; Maroupulos, Gd; Zurzolo, C; Taglialatela, Maurizio; Andria, G; Sebastio, G. |
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Opzioni
Scopri
Tipologia
- 1 Contributo su Rivista 155
- 1 Contributo su Rivista::1.1 Articolo in rivista 155
Data di pubblicazione
- 2020 - 2024 14
- 2010 - 2019 44
- 2000 - 2009 37
- 1990 - 1999 43
- 1984 - 1989 17
Rivista
- MOLECULAR PHARMACOLOGY 9
- BIOPHYSICAL JOURNAL 6
- EUROPEAN JOURNAL OF PHARMACOLOGY 6
- THE JOURNAL OF BIOLOGICAL CHEMISTRY 6
- PHARMACOLOGICAL RESEARCH 5
- THE JOURNAL OF NEUROSCIENCE 5
- THE JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS 5
- JOURNAL OF NEUROCHEMISTRY 4
- ANNALS OF THE NEW YORK ACADEMY OF SCIENCES 3
- BIOCHEMICAL PHARMACOLOGY 3
Keyword
- Kv7 channels 5
- KCNQ2 4
- Retigabine 4
- channelopathies 3
- epilepsy 3
- Humans 3
- Animals 2
- CHO Cells 2
- Cricetulus 2
- Epilepsy 2
Lingua
- eng 59
Accesso al fulltext
- no fulltext 155
Appartenenza
- DIPARTIMENTO DI MEDICINA E DI SCIENZE DELLA SALUTE 155