TAGLIALATELA, Maurizio

TAGLIALATELA, Maurizio  

DIPARTIMENTO DI MEDICINA E DI SCIENZE DELLA SALUTE  

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Risultati 1 - 20 di 166 (tempo di esecuzione: 0.03 secondi).
Titolo Data di pubblicazione Autore(i) File
"Janus face" of nitric oxide action on plasma membrane and intracellular ionic channels 1-gen-2001 Taglialatela, Maurizio; Pannaccione, A; Cataldi, M; Castaldo, P; Secondo, A; Iossa, S; Di Renzo, Gf; Annunziato, L.
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 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.
Activation and Desensitization of Trpv1 Channels in Sensory Neurons by the Peroxisome Proliferator-Activated Receptor α Agonist Palmitoylethanolamide 1-gen-2013 Ambrosino, P; Soldovieri, Maria Virginia; Russo, Claudio; Taglialatela, Maurizio
Activation of Kv7 potassium channels inhibits intracellular Ca2+ increases triggered by TRPV1-mediated pain-inducing stimuli in F11 immortalized sensory neurons 1-gen-2019 Ambrosino, P.; Soldovieri, M. V.; Di Zazzo, E.; Paventi, G.; Iannotti, F. A.; Mosca, I.; Miceli, F.; Franco, C.; Canzoniero, L. M. T.; Taglialatela, M.
Activation of pre-synaptic M-type K+ channels inhibits [H-3]d-aspartate release by reducing Ca2+ entry through P/Q-type voltage-gated Ca(2+)channels 1-gen-2009 Luisi, R; Panza, E; Barrese, V; Iannotti, Fa; Viggiano, Davide; Secondo, A; Canzoniero, Lm; Martire, M; Annunziato, L; Taglialatela, Maurizio
Adenosine receptors modulate the Na(+)-Ca2+ exchanger in cerebral nerve endings. 1-gen-1991 Taglialatela, Maurizio; Canzoniero, Lm; Rossi, Am; Mita, G; Direnzo, Gf; Annunziato, L.
AMPA- and P2X7-receptor-mediated facilitation of [H-3]D-aspartate release from nerve terminals isolated from the rat caudal brainstem 1-gen-2010 D'Amico, M; Samengo, I; Navarra, P; Taglialatela, Maurizio; Martire, M.
Atypical gating of M-type potassium channels conferred by mutations in uncharged residues in the S-4 region of KCNQ2 causing benign familial neonatal convulsions 1-gen-2007 Soldovieri, Maria Virginia; Cilio, Mr; Miceli, F; Bellini, G; del Giudice, Em; Castaldo, P; Hernandez, Cc; Shapiro, Ms; Pascotto, A; Annunziato, L; Taglialatela, Maurizio
Autism and developmental disability caused by KCNQ3 gain-of-function variants 1-gen-2019 Sands, T. T.; Miceli, F.; Lesca, G.; Beck, A. E.; Sadleir, L. G.; Arrington, D. K.; Schonewolf-Greulich, B.; Moutton, S.; Lauritano, A.; Nappi, P.; Soldovieri, M. V.; Scheffer, I. E.; Mefford, H. C.; Stong, N.; Heinzen, E. L.; Goldstein, D. B.; Perez, A. G.; Kossoff, E. H.; Stocco, A.; Sullivan, J. A.; Shashi, V.; Gerard, B.; Francannet, C.; Bisgaard, A. -M.; Tumer, Z.; Willems, M.; Rivier, F.; Vitobello, A.; Thakkar, K.; Rajan, D. S.; Barkovich, A. J.; Weckhuysen, S.; Cooper, E. C.; Taglialatela, M.; Cilio, M. R.
BARIUM BLOCKADE OF A CLONAL POTASSIUM CHANNEL AND ITS REGULATION BY A CRITICAL PORE RESIDUE 1-gen-1993 Taglialatela, Maurizio; Drewe, Ja; Brown, Am
Benign familial neonatal convulsions caused by altered gating of KCNQ2/KCNQ3 potassium channels 1-gen-2002 Castaldo, P; del Giudice, Em; Coppola, G; Pascotto, A; Annunziato, L; Taglialatela, Maurizio
Brain distribution of the Na+/Ca2+ exchanger-encoding genes NCX1, NCX2, and NCX3 and their related proteins in the central nervous system 1-gen-2002 Canitano, A; Papa, M; Boscia, F; Castaldo, P; Sellitti, S; Taglialatela, Maurizio; Annunziato, L.