BARONE, VIRGINIA

BARONE, VIRGINIA  

Dipartimento di Medicina Molecolare e dello Sviluppo  

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Risultati 1 - 20 di 43 (tempo di esecuzione: 0.0 secondi).
Titolo Data di pubblicazione Autore(i) File Abstract
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 -
A chloride conductance evoked by hypotonic shock in epithelial cells 1-gen-1991 Galietta, L. J. V.; Barone, V.; Gruenert, D. C.; Romeo, G. -
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. -
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. -
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. -
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. -
The gas 5 gene shows four alternative splicing patterns without coding for a protein 1-gen-2000 Raho, G.; Barone, V.; Rossi, D.; Philipson, L.; Sorrentino, V. -
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 -
Identification of the Cys 634->Tyr mutation of the RET proto-oncogene in a pedigree with Multiple Endocrine Neoplasia type 2A and localized cutaneous lichen amyloidosis 1-gen-1994 Ceccherini, I.; Romei, C.; Barone, V.; Pacini, F.; Martino, E.; Loviselli, A.; Pinchera, A.; Romeo, G. -
Increased Susceptibility to Cortical Spreading Depression in the Mouse Model of Familial Hemiplegic Migraine Type 2 1-gen-2011 Leo, Loredana; Gherardini, Lisa; Barone, Virginia; DE FUSCO, Maurizio; Pietrobon, Daniela; Pizzorusso, Tommaso; Casari, Giorgio -
Intracellular Ca(2+) release channels in evolution 1-gen-2000 Sorrentino, V.; Barone, V.; Rossi, D. -