Sfoglia per Autore
LOSS OF HETEROZYGOSITY OF IMPRINTED GENES IN SV40 T/T ANTIGEN-INDUCED HEPATOCELLULAR CARCINOMAS
1995 Casola, S; Ungaro, P; Pedone, Paolo Vincenzo; Lazzaro, D; Fattori, E; Ciliberto, G; Zarrilli, R; Bruni, Cb; Riccio, Andrea
Activation of fetal promoters of insulinlike growth factor II gene in hepatitis C virus-related chronic hepatitis, cirrhosis, and hepatocellular carcinoma
1996 Nardone, G; Romano, Marco; Calabro, A; Pedone, Paolo Vincenzo; Desio, I; Persico, M; Budillon, G; Bruni, Cb; Riccio, Andrea; Zarrilli, R.
Expression and parental imprinting of the H19 gene in human rhabdomyosarcoma
1997 Casola, S; Pedone, Paolo Vincenzo; Cavazzana, Ao; Basso, G; Luksch, R; Damore, Esg; Carli, M; Bruni, Cb; Riccio, Andrea
Relaxation of insulin-like growth factor-2 imprinting in rat cultured cells
1997 Ungaro, P; Casola, S; Vernucci, M; Pedone, Paolo Vincenzo; Bruni, Cb; Riccio, Andrea
Role of histone acetylation and DNA methylation in the maintenance of the imprinted expression of the H19 and Igf2 genes
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
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
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
2002 Cerrato, Flavia; Vernucci, M; Pedone, Paolo Vincenzo; Chiariotti, L; Sebastio, G; Bruni, Cb; Riccio, Andrea
The Arabidopsis SUPERMAN protein is able to specifically bind DNA through its single Cys2-His2 zinc finger motif
2002 Dathan, N; Zaccaro, L; Esposito, Sabrina; Isernia, Carla; Omichinski, Jg; Riccio, Andrea; Pedone, C; Di Blasio, B; Fattorusso, Roberto; Pedone, Paolo Vincenzo
Paternal imprints can be established on the maternal Igf2-H19 locus without altering replication timing of DNA
2003 Cerrato, Flavia; Dean, W; Davies, K; Kagotani, K; Mitsuya, K; Okumura, K; Riccio, Andrea; Reik, W.
Developmentally regulated functions of the H19 differentially methylated domain
2004 Vernucci, M.; Cerrato, Flavia; Pedone, Paolo Vincenzo; Dandolo, L.; Bruni, C. B.; Riccio, Andrea
Microdeletions in the human H19 DMR result in loss of IGF2 imprinting and Beckwith-Wiedemann syndrome
2004 Sparago, Angela; Cerrato, Flavia; Vernucci, M.; BATTISTA FERRERO, G.; CIRILLO SILENGO, M.; Riccio, Andrea
The two-domain hypothesis in Beckwith-Wiedemann syndrome: autonomous imprinting of the telomeric domain of the distal chromosome 7 cluster
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
2005 Cerrato, Flavia; Sparago, A; Farina, L; Ferrero, Gb; Silengo, Mc; Riccio, Andrea
Molecular subtypes and phenotypic expression of Beckwith-Wiedemann syndrome
2005 Cooper, Wn; Luharia, A; Evans, Ga; Raza, H; Haire, Ac; Grundy, R; Bowdin, Sc; Riccio, Andrea; Sebastio, G; Bliek, J; Schofield, Pn; Reik, W; Macdonald, F; Maher, Er
Perlman syndrome: Clinical report and nine-year follow-up
2005 Piccione, M; Ceeconi, M; Giuffre, M; Lo Curto, M; Malacarne, M; Piro, E; Riccio, Andrea; Corsello, G.
Familial posterior helical ear pits
2007 Guala, A; Guarino, R; Sparago, A; Riccio, Andrea; Franceschini, P.
Mechanisms causing imprinting defects in familial Beckwith-Wiedemann syndrome with Wilms' tumour
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
The H19 locus acts in vivo as a tumor suppressor
2008 Yoshimizu, T; Miroglio, A; Ripoche, Ma; Gabory, A; Vernucci, M; Riccio, Andrea; Colnot, S; Godard, C; Terris, B; Jammes, H; Dandolo, L.
Different mechanisms cause imprinting defects at the IGF2/H19 locus in Beckwith - Wiedemann syndrome and Wilms' tumour
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
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
LOSS OF HETEROZYGOSITY OF IMPRINTED GENES IN SV40 T/T ANTIGEN-INDUCED HEPATOCELLULAR CARCINOMAS | 1-gen-1995 | Casola, S; Ungaro, P; Pedone, Paolo Vincenzo; Lazzaro, D; Fattori, E; Ciliberto, G; Zarrilli, R; Bruni, Cb; Riccio, Andrea | |
Activation of fetal promoters of insulinlike growth factor II gene in hepatitis C virus-related chronic hepatitis, cirrhosis, and hepatocellular carcinoma | 1-gen-1996 | Nardone, G; Romano, Marco; Calabro, A; Pedone, Paolo Vincenzo; Desio, I; Persico, M; Budillon, G; Bruni, Cb; Riccio, Andrea; Zarrilli, R. | |
Expression and parental imprinting of the H19 gene in human rhabdomyosarcoma | 1-gen-1997 | Casola, S; Pedone, Paolo Vincenzo; Cavazzana, Ao; Basso, G; Luksch, R; Damore, Esg; Carli, M; Bruni, Cb; Riccio, Andrea | |
Relaxation of insulin-like growth factor-2 imprinting in rat cultured cells | 1-gen-1997 | Ungaro, P; Casola, S; Vernucci, M; Pedone, Paolo Vincenzo; Bruni, Cb; Riccio, Andrea | |
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 | |
The Arabidopsis SUPERMAN protein is able to specifically bind DNA through its single Cys2-His2 zinc finger motif | 1-gen-2002 | Dathan, N; Zaccaro, L; Esposito, Sabrina; Isernia, Carla; Omichinski, Jg; Riccio, Andrea; Pedone, C; Di Blasio, B; Fattorusso, Roberto; Pedone, Paolo Vincenzo | |
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. | |
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 | |
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 | |
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 | |
Molecular subtypes and phenotypic expression of Beckwith-Wiedemann syndrome | 1-gen-2005 | Cooper, Wn; Luharia, A; Evans, Ga; Raza, H; Haire, Ac; Grundy, R; Bowdin, Sc; Riccio, Andrea; Sebastio, G; Bliek, J; Schofield, Pn; Reik, W; Macdonald, F; Maher, Er | |
Perlman syndrome: Clinical report and nine-year follow-up | 1-gen-2005 | Piccione, M; Ceeconi, M; Giuffre, M; Lo Curto, M; Malacarne, M; Piro, E; Riccio, Andrea; Corsello, G. | |
Familial posterior helical ear pits | 1-gen-2007 | Guala, A; Guarino, R; Sparago, A; Riccio, Andrea; Franceschini, P. | |
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 | |
The H19 locus acts in vivo as a tumor suppressor | 1-gen-2008 | Yoshimizu, T; Miroglio, A; Ripoche, Ma; Gabory, A; Vernucci, M; Riccio, Andrea; Colnot, S; Godard, C; Terris, B; Jammes, H; Dandolo, L. | |
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 |
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