IRIS

CERRATO, Flavia

CERRATO, Flavia  

Dipartimento di Scienze e Tecnologie Ambientali Biologiche e Farmaceutiche (DISTABiF)  

Mostra records
Risultati 1 - 20 di 42 (tempo di esecuzione: 0.013 secondi).
Titolo Data di pubblicazione Autore(i) File
A novel large deletion of the ICR1 region including H19 and putative enhancer elements 1-gen-2015 Fryssira, Helen; Amenta, Stella; Kanber, Deniz; Sofocleous, Christalena; Lykopoulou, Evangelia; Kanaka Gantenbein, Christina; Cerrato, Flavia; Lüdecke, Hermann Josef; Bens, Susanne; Riccio, Andrea; Buiting, Karin
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
Assisted Reproductive Techniques and Risk of Beckwith-Wiedemann Syndrome 1-gen-2017 Mussa, Alessandro; Molinatto, Cristina; Cerrato, Flavia; Palumbo, Orazio; Carella, Massimo; Baldassarre, Giuseppina; Carli, Diana; Peris, Clementina; Riccio, Andrea; Ferrero, Giovanni Battista
Beckwith-Wiedemann Syndrome 1-gen-2019 Mussa, A; Kalish, J; Cerrato, F; Riccio, A; Ferrero, Gb
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
Both Epimutations and Chromosome Aberrations Affect Multiple Imprinted Loci in Aggressive Wilms Tumors 1-gen-2020 Pignata, L.; Palumbo, O.; Cerrato, F.; Acurzio, B.; de Alava, E.; Roma, J.; Gallego, S.; Mora, J.; Carella, M.; Riccio, A.; Verde, G.
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
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
DNA Methylation in the Diagnosis of Monogenic Diseases 1-gen-2020 Cerrato, F.; Sparago, A.; Ariani, F.; Brugnoletti, F.; Calzari, L.; Coppede, F.; De Luca, A.; Gervasini, C.; Giardina, E.; Gurrieri, F.; Lo Nigro, C.; Merla, G.; Miozzo, M.; Russo, S.; Sangiorgi, E.; Sirchia, S. M.; Squeo, G. M.; Tabano, S.; Tabolacci, E.; Torrente, I.; Genuardi, M.; Neri, G.; Riccio, A.
EFFECTS OF PROLONGED WAKEFULNESS: THE ROLE OF PERIOD3 GENOTYPES AND PERSONALITY TRAITS 1-gen-2013 Barbato, Giuseppe; Costanzo, A; della Monica, C; D'Onofrio, P; Cerrato, Flavia; De Padova, V.
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.
Humanized H19/Igf2 locus reveals diverged imprinting mechanism between mouse and human and reflects Silver-Russell syndrome phenotypes 1-gen-2016 Hur, Stella K.; Freschi, Andrea; Ideraabdullah, Folami; Thorvaldsen, Joanne L.; Luense, Lacey J.; Weller, Angela H.; Berger, Shelley L.; Cerrato, Flavia; Riccio, Andrea; Bartolomei, Marisa S.
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
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
Is ZFP57 binding to H19/IGF2: IG-DMR affected in Silver-Russell syndrome? 1-gen-2018 Sparago, Angela; Cerrato, Flavia; Riccio, Andrea
Looking for CDKN1C enhancers 1-gen-2014 Cerrato, Flavia; De Crescenzo, A; Riccio, Andrea
Loss-of-function maternal-effect mutations of PADI6 are associated with familial and sporadic Beckwith-Wiedemann syndrome with multi-locus imprinting disturbance 1-gen-2020 Cubellis, M. V.; Pignata, L.; Verma, A.; Sparago, A.; Del Prete, R.; Monticelli, M.; Calzari, L.; Antona, V.; Melis, D.; Tenconi, R.; Russo, S.; Cerrato, F.; Riccio, A.
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
Microdeletion and IGF2 loss of imprinting in a cascade causing Beckwith-Wiedemann syndrome with Wilms' tumor (multiple letters) 1-gen-2005 Prawitt D.; Enklaar T.; Gartner-Rupprecht B.; Spangenberg C.; Lausch E.; Reutzel D.; Fees S.; Korzon M.; Brozek I.; Limon J.; Housman D.E.; Pelletier J.; Zabel B.; Cerrato F.; Sparago A.; Farina L.; Ferrero G.B.; Silengo M.C.; Riccio A.