BARONE, VIRGINIA

BARONE, VIRGINIA  

Dipartimento di Medicina Molecolare e dello Sviluppo  

Mostra records
Risultati 1 - 20 di 45 (tempo di esecuzione: 0.0 secondi).
Titolo Data di pubblicazione Autore(i) File Abstract
A chloride conductance evoked by hypotonic shock in epithelial cells 1-gen-1991 Galietta, L. J. V.; Barone, V.; Gruenert, D. C.; Romeo, G. -
A forskolin and verapamil sensitive potassium current in human tracheal cells 1-gen-1991 Galietta, L. J. V.; Rasola, A.; Barone, V.; Gruenert, D. C.; Romeo, G. -
A mutation in the CASQ1 gene causes a vacuolar myopathy with accumulation of sarcoplasmic reticulum protein aggregates 1-gen-2014 Rossi, D.; Vezzani, B.; Galli, L.; Paolini, C.; Toniolo, L.; Pierantozzi, E.; Spinozzi, S.; Barone, V.; Pegoraro, E.; Bello, L.; Cenacchi, G.; Vattemi, G.; Tomelleri, G.; Ricci, G.; Siciliano, G.; Protasi, F.; Reggiani, C.; Sorrentino, V. -
A novel FLNC frameshift and an OBSCN variant in a family with distal muscular dystrophy 1-gen-2017 Rossi, Daniela; Palmio, Johanna; Evilã¤, Anni; Galli, Lucia; Barone, Virginia; Caldwell, Tracy A.; Policke, Rachel A.; Aldkheil, Esraa; Berndsen, Christopher E.; Wright, Nathan T.; Malfatti, Edoardo; Brochier, Guy; Pierantozzi, Enrico; Jordanova, Albena; Guergueltcheva, Velina; Romero, Norma Beatriz; Hackman, Peter; Eymard, Bruno; Udd, Bjarne; Sorrentino, Vincenzo -
A novel mutation in the ATP1A2 gene causes alternating hemiplegia of childhood 1-gen-2004 Bassi, M. T.; Bresolin, N.; Tonelli, A.; Nazos, K.; Crippa, F.; Baschirotto, C.; Zucca, C.; Bersano, A.; Dolcetta, D.; Boneschi, F. M.; Barone, V.; Casari, G. -
Binding of an ankyrin-1 isoform to obscurin suggests a molecular link between the sarcoplasmic reticulum and myofibrils in striated muscles 1-gen-2003 Bagnato, P.; Barone, V.; Giacomello, E.; Rossi, D.; Sorrentino, V. -
Characterization of chloride and cation channels in cultured human keratinocytes 1-gen-1991 Galietta, L. J. V.; Barone, V.; DE LUCA, M.; Romeo, G. -
Chemical characterization and antihypertensive effects of locular gel and serum of Lycopersicum esculentum L. var. “Camone” tomato in spontaneously hypertensive rats 1-gen-2020 Marcolongo, Paola; Gamberucci, Alessandra; Tamasi, Gabriella; Pardini, Alessio; Bonechi, Claudia; Rossi, Claudio; Giunti, Roberta; Barone, Virginia; Borghini, Annalisa; Fiorenzani, Paolo; Frosini, Maria; Valoti, Massimo; Pessina, Federica -
Close linkage with the RET proto-oncogene and boundaries of deletion mutations in autosamal dominant Hirschsprung disease 1-gen-1993 Yin, L.; Ceccherini, I.; Pasini, B.; Matera, I.; Bicocchi, M. P.; Barone, V.; Bocciardi, R.; Kaariainen, H.; Weber, D.; Devoto, M.; Romeo, G. -
Co-Expression of Podoplanin and CD44 in Proliferative Vitreoretinopathy Epiretinal Membranes 1-gen-2023 Bonente, Denise; Bianchi, Laura; De Salvo, Rossana; Nicoletti, Claudio; De Benedetto, Elena; Bacci, Tommaso; Bini, Luca; Inzalaco, Giovanni; Franci, Lorenzo; Chiariello, Mario; Tosi, Gian Marco; Bertelli, Eugenio; Barone, Virginia -
Contractile impairment and structural alterations of skeletal muscles from knockout mice lacking type 1 and type 3 ryanodine receptors 1-gen-1998 Barone, V.; Bertocchini, F.; Bottinelli, R.; Protasi, F.; Allen, P. D.; Armstrong, C. F.; Reggiani, C.; Sorrentino, V. -
Contribution of ryanodine receptor type 3 to Ca(2+) sparks in embryonic mouse skeletal muscle 1-gen-1999 Conklin, M. W.; Barone, V.; Sorrentino, V.; Coronado, R. -
Deletion of the ryanodine receptor type 3 (RyR3) impairs forms of synaptic plasticity and spatial learning 1-gen-1999 Balschun, D.; Wolfer, D. P.; Bertocchini, F.; Barone, V.; Conti, A.; Zuschratter, A.; Missiaen, L.; Lipp, H. P.; Frey, J. U.; Sorrentino, V. -
DNA polymorphisms and conditions for SSCP analysis of the 20 exons of the RET proto-oncogene 1-gen-1994 Ceccherini, I.; Hofstra, R. M. W.; Yin, L.; Stulp, R. P.; Barone, V.; Stelwagen, T.; Bocciardi, R.; Nijeveen, H.; Bolino, A.; Seri, M.; Ronchetto, P.; Pasini, B.; Bozzano, M.; C. H. C. M. BUYS, C. H. C. M.; Romeo, G. -
Examining the impact of maternal individual features on children’s behavioral problems in adoptive families: The role of maternal temperament and neurobiological markers 1-gen-2018 Ozturk, Yagmur; Barone, Virginia; Barone, Lavinia -
Exclusion of linkage between RET and Neuronal Intestinal Dysplasia Type B 1-gen-1996 Barone, V.; Weber, D.; Yin, L.; Brancolini, V.; Devoto, M.; Romeo, G. -
Frequency of RET mutations in long and short segment Hirschsprung disease 1-gen-1997 Seri, M.; Yin, L.; Barone, V.; Bolino, A.; Celli, J.; Bocciardi, R.; Pasini, B.; Ceccherini, I.; Lerone, M.; Kristoffersson, U.; Larsson, L. T.; Casasa, J. M.; Abramowicz, M. J.; Vanderwinden, J. M.; Kravcenkiene, I.; Baric, I.; Silengo, M.; Martucciello, G.; Romeo, G. -
Heterogeneity and low detection rate of RET mutations in Hirschsprung disease 1-gen-1994 Yin, L.; Barone, V.; Seri, M.; Bolino, A.; Bocciardi, R.; Ceccherini, I.; Pasini, B.; Tocco, T.; Lerone, M.; Cywes, S.; Moore, S.; Vanderwinden, J. M.; Abramowicz, M. J.; Kristoffersson, U.; Larsson, L. Y.; Hamel, B. C. J.; Silengo, M.; Martucciello, G.; Romeo, G. -
Homer proteins and InsP(3) receptors co-localise in the longitudinal sarcoplasmic reticulum of skeletal muscle fibres 1-gen-2002 Salanova, M.; Priori, G.; Barone, V.; Intravaia, E.; Flucher, B.; Ciruela, F.; Mcilhinney, R. A.; Parys, J. B.; Mikoshiba, K.; Sorrentino, V. -
Identification and characterization of three novel mutations in the CASQ1 gene in four patients with tubular aggregate myopathy 1-gen-2017 Barone, Virginia; DEL RE, Valeria; Gamberucci, Alessandra; Polverino, Valentina; Galli, Lucia; Rossi, Daniela; Costanzi, Elisa; Toniolo, Luana; Berti, Gianna; Malandrini, Alessandro; Ricci, Giulia; Siciliano, Gabriele; Vattemi, Gaetano; Tomelleri, Giuliano; Pierantozzi, Enrico; Spinozzi, Simone; Volpi, Nila; Fulceri, Rosella; Battistutta, Roberto; Reggiani, Carlo; Sorrentino, Vincenzo -