VARGIOLU, MANUELA
VARGIOLU, MANUELA
CIRI SCIENZE DELLA VITA E TECNOLOGIE PER LA SALUTE
Assegnisti
Prucalopride exerts neuroprotection in human enteric neurons
2016 Bianco, F; Bonora, E; Natarajan, D; Vargiolu, M; Thapar, N; Torresan, F; Giancola, F; Boschetti, E; Volta, U; Bazzoli, F; Mazzoni, M; Seri, M; Clavenzani, P; Stanghellini, V; Sternini, C; De Giorgio, R.
Cytogenetic and molecular characterization of a recombinant X chromosome in a family with a severe neurologic phenotype and macular degeneration
2015 Magini, Pamela; Poscente, Monica; Ferrari, Simona; Vargiolu, Manuela; Bacchelli, Elena; Graziano, Claudio; Wischmeijer, Anita; Turchetti, Daniela; Malaspina, Elisabetta; Marchiani, Valentina; Cordelli, Duccio Maria; Franzoni, Emilio; Romeo, Giovanni; Seri, Marco
Su1852 The 5-HT4 Selective Agonist Prucalopride Exerts Neural and Epithelial Protective Effects In Vitro
2015 Bianco, Francesca; Bonora, Elena; Vargiolu, Manuela; Giancola, Fiorella; Natarajan, Dipa; Thapar, Nikhil; Stanghellini, Vincenzo; Seri, Marco; Clavenzani, Paolo; DE GIORGIO, Roberto
Corrigendum: Maternally inherited genetic variants of CADPS2 are present in Autism Spectrum Disorders and Intellectual Disability patients(EMBO Mol Med, (2014), 6, (795–809), 10.1002/emmm.201303235)
2014 Bonora, E.; Graziano, C.; Minopoli, F.; Bacchelli, E.; Magini, P.; Diquigiovanni, C.; Lomartire, S.; Bianco, F.; Vargiolu, M.; Parchi, P.; Marasco, E.; Mantovani, V.; Rampoldi, L.; Trudu, M.; Parmeggiani, A.; Battaglia, A.; Mazzone, L.; Tortora, G.; Maestrini, E.; Seri, M.; Romeo, G.
Maternally inherited genetic variants of CADPS2 are present in Autism Spectrum Disorders and Intellectual Disability patients.
2014 Bonora E;Graziano C;Minopoli F;Bacchelli E;Magini P;Diquigiovanni C;Lomartire S;Bianco F;Vargiolu M;Parchi P;Marasco E;Mantovani V;Rampoldi L;Trudu M;Parmeggiani A;Battaglia A;Mazzone L;Tortora G;Maestrini E;Seri M;Romeo G;IMGSAC
The FOXE1 locus is a major genetic determinant for familial nonmedullary thyroid carcinoma
2014 Bonora, Elena; Rizzato, Cosmeri; Diquigiovanni, Chiara; Oudot-Mellakh, Tiphaine; Campa, Daniele; Vargiolu, Manuela; Guedj, Mickaël; Mckay, James D.; Romeo, Giovanni; Canzian, Federico; Lesueur, Fabienne
The KIT Gene Is Associated with the English Spotting Coat Color Locus and Congenital Megacolon in Checkered Giant Rabbits (Oryctolagus cuniculus)
2014 Luca Fontanesi;Manuela Vargiolu;Emilio Scotti;Rocco Latorre;Maria Simonetta Faussone Pellegrini;Maurizio Mazzoni;Martina Asti;Roberto Chiocchetti;Giovanni Romeo;Paolo Clavenzani;Roberto De Giorgio
Apolipoprotein B is a new target of the GDNF/RET and ET-3/EDNRB signalling pathways
2012 C. Evangelisti;F. Bianco;L. M. Pradella;A. Puliti;A. Goldoni;I. Sbrana;M. Rossi;M. Vargiolu;M. Seri;G. Romeo;V. Stanghellini;R. de Giorgio;E. Bonora
Evidence of RET/GDNF-related apolipoprotein B (APOB) activation and altered expression in patients with chronic intestinal pseudo-obstruction (CIPO)
2012 Bianco F; Bonora E; Cogliandro R; Vargiolu M; Giancola F; Boschetti E; Seri M; Barbara G; Corinaldesi R; Stanghellini V; De Giorgio R
Caratterizzazione genetico-molecolare e morfologica di un modello sperimentale di megacolon congenito non agangliare.
2011 Latorre R.; Clavenzani P.; Mazzoni M.; Asti M.; Fontanesi L.; Vargiolu M.; Faussone Pellegrini MS.; Barbara G.; Corinaldesi R.; Stanghellini V.; De Giorgio R.
Molecular and Pathological characterization of a non-aganglionic congenital megacolon in the rabbit
2011 Fontanesi L.; Vargiolu M.; Scotti E.; Faussone Pellegrini MS.; Clavenzani P.; Asti M.; Mazzoni M.; Latorre R.; Chiocchetti R.; Loche E.; Naponelli V.; Russo V.; Stanghellini V.; Corinaldesi R.; De Giorgio R.
Endothelin receptor B (EDNRB) is not the causative gene of the English spotting locus in the domestic rabbit (Oryctolagus cuniculus)
2010 Fontanesi L.; Vargiolu M.; Scotti E.; Mazzoni M.; Clavenzani P.; De Giorgio R.; Romeo G.; Russo V.
The RET51/FKBP52 complex and its involvement in Parkinson disease.
2010 Fusco D; Vargiolu M; Vidone M; Mariani E; Pennisi LF; Bonora E; Capellari S; Dirnberger D; Baumeister R; Martinelli P; Romeo G.
Aryl hydrocarbon receptor interacting protein mutations seem not to associate with familial non-medullary thyroid cancer.
2009 Raitila A; Georgitsi M; Bonora E; Vargiolu M; Tuppurainen K; Mäkinen MJ; Vierimaa O; Salmela PI; Launonen V; Vahteristo P; Aaltonen LA; Romeo G; Karhu A.
The FAGenomicH project: Towards a whole candidate gene approach to identify markers associated with fatness and production traits in pigs and investigate the pig as a model for human obesity
2009 Fontanesi L.; Fronza R.; Scotti E.; Colombo M.; Speroni C.; Tognazzi L.; Galimberti G.; Calò DG; Bonora E.; Vargiolu M.; Romeo G.; Casadio R.; Russo V.
The tyrosine kinase receptor RET interacts in vivo with aryl hydrocarbon receptor-interacting protein to alter survivin availability.
2009 Vargiolu M; Fusco D; Kurelac I; Dirnberger D; Baumeister R; Morra I; Melcarne A; Rimondini R; Romeo G; Bonora E
The FAGenomicH project: a whole candidate gene approach to identify markers associated with fatness traits in pigs and investigate the pig as a model for human obesity
2008 Fontanesi L.; Fronza R.; Scotti E.; Galimberti G.; Calò D.G.; Bonora E.; Vargiolu M.; Colombo M.; Casadio R.; Romeo G.; Russo V.