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Titolo Data di pubblicazione Autore(i) File
Wilms tumor and constitutional epigenetic defects 1-gen-2008 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.
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
Silver-russell syndrome following in vitro fertilization 1-gen-2008 Douzgou, S; Mingarelli, R; Tarani, L; De Crescenzo, A; Riccio, Andrea
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
Silver-Russell Syndrome and Beckwith-Wiedemann Syndrome Phenotypes Associated with 11p Duplication in a Single Family 1-gen-2010 Cardarelli, L; Sparago, A; De Crescenzo, A; Nalesso, E; Zavan, B; Cubellis, Mv; Selicorni, A; Cavicchioli, P; Pozzan, Gb; Petrella, M; Riccio, Andrea
A case of Beckwith-Wiedemann syndrome caused by a cryptic 11p15 deletion encompassing the centromeric imprinted domain of the BWS locus 1-gen-2010 Zollino, M; Orteschi, D; Marangi, G; De Crescenzo, A; Pecile, V; Riccio, Andrea; Neri, G.
22q11.2 distal deletion syndrome: Description of a new case with truncus arteriosus type 2 and review 1-gen-2011 Garavelli, L; Rosato, S; Wischmeijer, A; Gelmini, C; Esposito, A; Mazzanti, L; Franchi, F; De Crescenzo, A; Palumbo, O; Carella, M; Riccio, Andrea
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
In Embryonic Stem Cells, ZFP57/KAP1 Recognize a Methylated Hexanucleotide to Affect Chromatin and DNA Methylation of Imprinting Control Regions 1-gen-2011 Quenneville, S; Verde, G; Corsinotti, A; Kapopoulou, A; Jakobsson, J; Offner, S; Baglivo, I; Pedone, Paolo Vincenzo; Grimaldi, G; Riccio, Andrea; Trono, D.
Disruption of genomic neighbourhood at the imprinted IGF2-H19 locus in Beckwith-Wiedemann syndrome and Silver-Russell syndrome 1-gen-2011 Nativio, R; Sparago, A; Ito, Y; Weksberg, R; Riccio, Andrea; Murrell, A.
Nephrological findings and genotype-phenotype correlation in Beckwith-Wiedemann syndrome 1-gen-2012 Mussa, A; Peruzzi, L; Chiesa, N; De Crescenzo, A; Russo, S; Melis, D; Tarani, L; Baldassarre, G; Larizza, L; Riccio, Andrea; Silengo, M; Ferrero, Gb
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
Gain of function in CDKN1C 1-gen-2012 Riccio, Andrea; Cubellis, Mv
Genetic and epigenetic mutations affect the DNA binding capability of human ZFP57 in transient neonatal diabetes type 1 1-gen-2013 Baglivo, Ilaria; Esposito, Sabrina; De Cesare, L; Rivellino, A; Sparago, A; Anvar, Z; Riso, V; Cammisa, Marco; Fattorusso, Roberto; Grimaldi, Giuseppe; Riccio, Andrea; Pedone, Paolo Vincenzo
Silver-Russell syndrome due to paternal H19/IGF2 hypomethylation in a twin girl born after in vitro fertilization 1-gen-2013 Cocchi, G; Marsico, C; Cosentino, A; Spadoni, C; Rocca, A; De Crescenzo, A; Riccio, Andrea
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.
Imprinting at the PLAGL1 domain is contained within a 70-kb CTCF/cohesin-mediated non-allelic chromatin loop 1-gen-2013 Iglesias Platas, I; Court, F; Camprubi, C; Sparago, A; Guillaumet Adkins, A; Martin Trujillo, A; Riccio, Andrea; Moore, G. E.; Monk, D.
Mostrati risultati da 41 a 60 di 125
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