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Role of histone acetylation and DNA methylation in the maintenance of the imprinted expression of the H19 and Igf2 genes 1-gen-1999 Pedone, Paolo Vincenzo; Pikaart, M. J.; Cerrato, Flavia; Vernucci, M.; Ungaro, P.; Bruni, C. B.; Riccio, Andrea
The H19 endodermal enhancer is required for Igf2 activation and tumor formation in experimental liver carcinogenesis 1-gen-2000 Vernucci, M; Cerrato, Flavia; Besnard, N; Casola, S; Pedone, Paolo Vincenzo; Bruni, Cb; Riccio, Andrea
Relaxation of insulin-like growth factor 2 imprinting and discordant methylation at KvDMR1 in two first cousins affected by Beckwith-Wiedemann and Klippel-Trenaunay-Weber syndromes 1-gen-2000 Sperandeo, Mp; Ungaro, P; Vernucci, M; Pedone, Paolo Vincenzo; Cerrato, Flavia; Perone, L; Casola, S; Cubellis, Mv; Bruni, Cb; Andria, G; Sebastio, G; Riccio, Andrea
The 5′ end of the KCNQ10T1 gene is hypomethylated in the Beckwith-Wiedemann syndrome 1-gen-2002 Cerrato, Flavia; Vernucci, M; Pedone, Paolo Vincenzo; Chiariotti, L; Sebastio, G; Bruni, Cb; Riccio, Andrea
Paternal imprints can be established on the maternal Igf2-H19 locus without altering replication timing of DNA 1-gen-2003 Cerrato, Flavia; Dean, W; Davies, K; Kagotani, K; Mitsuya, K; Okumura, K; Riccio, Andrea; Reik, W.
Microdeletions in the human H19 DMR result in loss of IGF2 imprinting and Beckwith-Wiedemann syndrome 1-gen-2004 Sparago, Angela; Cerrato, Flavia; Vernucci, M.; BATTISTA FERRERO, G.; CIRILLO SILENGO, M.; Riccio, Andrea
Developmentally regulated functions of the H19 differentially methylated domain 1-gen-2004 Vernucci, M.; Cerrato, Flavia; Pedone, Paolo Vincenzo; Dandolo, L.; Bruni, C. B.; Riccio, Andrea
The two-domain hypothesis in Beckwith-Wiedemann syndrome: autonomous imprinting of the telomeric domain of the distal chromosome 7 cluster 1-gen-2005 Cerrato, Flavia; Sparago, A.; DI MATTEO, I.; Zou, X.; Dean, W.; Sasaki, H.; Smith, P.; Genesio, R.; Bruggemann, M.; Reik, W.; Riccio, Andrea
Microdeletion and IGF2 loss of imprinting in a cascade causing Beckwith-Wiedemann syndrome with Wilms' tumor - Reply 1-gen-2005 Cerrato, Flavia; Sparago, A; Farina, L; Ferrero, Gb; Silengo, Mc; Riccio, Andrea
Mechanisms causing imprinting defects in familial Beckwith-Wiedemann syndrome with Wilms' tumour 1-gen-2007 Sparago, A; Russo, S; Cerrato, Flavia; Ferraiuolo, S; Castorina, P; Selicorni, A; Schwienbacher, C; Negrini, M; Ferrero, Gb; Silengo, Mc; Anichini, C; Larizza, L; Riccio, Andrea
High frequency of loss of heterozygosity at 11p15 and IGF2 overexpression are not related to clinical outcome in childhood adrenocortical tumors positive for the R337H TP53 mutation 1-gen-2008 Rosati, R; Cerrato, Flavia; Doghman, M; Pianovski, Mad; Parise, Ga; Custodio, G; Zambetti, Gp; Ribeiro, Rc; Riccio, Andrea; Figueiredo, Bc; Lalli, E.
Different mechanisms cause imprinting defects at the IGF2/H19 locus in Beckwith - Wiedemann syndrome and Wilms' tumour 1-gen-2008 Cerrato, Flavia; Sparago, A.; Verde, G.; DE CRESCENZO, A.; Citro, V.; Cubellis, M.; Rinaldi, M.; Boccuto, L.; Neri, G.; Magnani, C.; D'Angelo, P.; Collini, P.; Perrotti, D.; Sebastio, G.; Maher, E.; Riccio, Andrea
Distinct methylation changes at the IGF2-H19 locus in congenital growth disorders and cancer 1-gen-2008 Murrell, Adele; Ito, Yoko; Verde, Gaetano; Huddleston, Joanna; Woodfine, Kathryn; Cirillo Silengo, Margherita; Spreafico, Filippo; Perotti, Daniela; De Crescenzo, Agostina; Sparago, Angela; Cerrato, Flavia; Riccio, Andrea
MS-MLPA is a specific and sensitive technique for detecting all chromosome 11p15.5 imprinting defects of BWS and SRS in a single-tube experiment 1-gen-2008 Priolo, M; Sparago, A; Mammi, C; Cerrato, Flavia; Lagana, C; Riccio, Andrea
Inherited and sporadic epimutations at the IGF2-H19 locus in beckwith-wiedemann syndrome and wilms' tumor 1-gen-2009 Riccio, Andrea; Sparago, A; Verde, G; DE CRESCENZO, A; Citro, V; Cubellis, Mv; Ferrero, Gb; Silengo, Mc; Russo, S; Larizza, L; Cerrato, Flavia
Hypomethylation at multiple maternally methylated imprinted regions including PLAGL1 and GNAS loci in Beckwith-Wiedemann syndrome 1-gen-2009 Bliek, J.; Verde, G.; Callaway, J.; Maas, S.; DE CRESCENZO, A.; Sparago, A.; Cerrato, Flavia; Russo, S.; Ferraiuolo, S.; Rinaldi, M. M.; Fischetto, R.; Lalatta, F.; Giordano, L.; Ferrari, P.; Cubellis, M. V.; Larizza, L.; Temple, K.; Mannes, M.; Mackay, D.; Riccio, Andrea
BEHAVIORAL CHANGES FOLLOWING TOTAL SLEEP DEPRIVATION. THE ROLE OF PER3 POLYMORPHISM AND OF PERSONALITY FACTORS 1-gen-2010 Barbato, Giuseppe; Costanzo, A; della Monica, C; Cerrato, Flavia
A novel microdeletion in the IGF2/H19 imprinting centre region defines a recurrent mutation mechanism in familial Beckwith-Wiedemann syndrome 1-gen-2011 De Crescenzo, A; Coppola, F; Falco, P; Bernardo, I; Ausanio, G; Cerrato, Flavia; Falco, L; Riccio, Andrea
The KCNQ1OT1 imprinting control region and non-coding RNA: New properties derived from the study of Beckwith-Wiedemann syndrome and Silver-Russell syndrome cases 1-gen-2012 Chiesa, N; De Crescenzo, A; Mishra, K; Perone, L; Carella, M; Palumbo, O; Mussa, A; Sparago, A; Cerrato, Flavia; Russo, S; Lapi, E; Cubellis, Mv; Kanduri, C; Silengo, Mc; Riccio, Andrea; Ferrero, Gb
Paternal deletion of the 11p15.5 centromeric-imprinting control region is associated with alteration of imprinted gene expression and recurrent severe intrauterine growth restriction 1-gen-2013 De Crescenzo, A; Sparago, A; Cerrato, Flavia; Palumbo, O; Carella, M; Miceli, M; Bronshtein, M; Riccio, Andrea; Yaron, Y.
Mostrati risultati da 1 a 20 di 48
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