IRIS

RICCIO, Andrea

RICCIO, Andrea  

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

Mostra records
Risultati 1 - 20 di 130 (tempo di esecuzione: 0.044 secondi).
Titolo Data di pubblicazione Autore(i) File
(Epi)genotype-phenotype correlations in Beckwith-Wiedemann syndrome 1-gen-2016 Mussa, Alessandro; Russo, Silvia; de Crescenzo, Agostina; Freschi, Andrea; Calzari, Luciano; Maitz, Silvia; Macchiaiolo, Marina; Molinatto, Cristina; Baldassarre, Giuseppina; Mariani, Milena; Tarani, Luigi; Bedeschi, Maria Francesca; Milani, Donatella; Melis, Daniela; Bartuli, Andrea; Cubellis, Maria Vittoria; Selicorni, Angelo; Cirillo Silengo, Margherita; Larizza, Lidia; Riccio, Andrea; Ferrero, Giovanni Battista
(Epi)genotype-phenotype correlations in Beckwith-Wiedemann syndrome: A paradigm for genomic medicine 1-gen-2016 Mussa, A.; Russo, S.; Larizza, L.; Riccio, Andrea; Ferrero, G. B.
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 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.
A common response element mediates differential effects of phorbol esters and forskolin on type‐1 plasminogen activator inhibitor gene expression in human breast carcinoma cells 1-gen-1994 Knudsen, H; Olesen, T; Riccio, Andrea; Ungaro, P; Christensen, L; Andreasen, Pa
A KHDC3L mutation resulting in recurrent hydatidiform mole causes genome-wide DNA methylation loss in oocytes and persistent imprinting defects post-fertilisation 1-gen-2019 Demond, H.; Anvar, Z.; Jahromi, B. N.; Sparago, A.; Verma, A.; Davari, M.; Calzari, L.; Russo, S.; Jahromi, M. A.; Monk, D.; Andrews, S.; Riccio, A.; Kelsey, G.
A maternal-effectPadi6variant causes nuclear and cytoplasmic abnormalities in oocytes, as well as failure of epigenetic reprogramming and zygotic genome activation in embryos 1-gen-2024 Giaccari, Carlo; Cecere, Francesco; Argenziano, Lucia; Pagano, Angela; Galvao, Antonio; Acampora, Dario; Rossi, Gianna; Hay Mele, Bruno; Acurzio, Basilia; Coonrod, Scott; Cubellis, Maria Vittoria; Cerrato, Flavia; Andrews, Simon; Cecconi, Sandra; Kelsey, Gavin; Riccio, Andrea
A new case of de novo 6q24.2-q25.2 deletion on paternal chromosome 6 with growth hormone deficiency: A twelve-year follow-up and literature review 1-gen-2015 Stagi, Stefano; Lapi, Elisabetta; Pantaleo, Marilena; Carella, Massimo; Petracca, Antonio; De Crescenzo, Agostina; Zelante, Leopoldo; Riccio, Andrea; de Martino, Maurizio
A novel iPSC-based model of ICF syndrome subtype 2 recapitulates the molecular phenotype of ZBTB24 deficiency 1-gen-2024 Lullo, Vincenzo; Cecere, Francesco; Batti, Saveria; Allegretti, Sara; Morone, Barbara; Fioriniello, Salvatore; Pisapia, Laura; Genesio, Rita; Della Ragione, Floriana; Giardino, Giuliana; Pignata, Claudio; Riccio, Andrea; Matarazzo, Maria R.; Strazzullo, Maria
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
A novel missense variant in PNLDC1 associated with nonobstructive azoospermia 1-gen-2024 Rahimian, Mouness; Askari, Masomeh; Salehi, Najmeh; Jaafarinia, Mojtaba; Forouzanfar, Mohsen; Almadani, Navid; Riccio, Andrea; Totonchi, Mehdi
A paternally inherited 1.4 kb deletion of the 11p15.5 imprinting center 2 is associated with a mild familial Silver–Russell syndrome phenotype 1-gen-2021 Mio, C.; Allegri, L.; Passon, N.; Bregant, E.; Demori, E.; Franzoni, A.; Driul, D.; Riccio, A.; Damante, G.; Baldan, F.
A splicing mutation of the HMGA2 gene is associated with Silver-Russell syndrome phenotype 1-gen-2015 De Crescenzo, Agostina; Citro, Valentina; Freschi, Andrea; Sparago, Angela; Palumbo, Orazio; Cubellis, Maria Vittoria; Carella, Massimo; Castelluccio, Pia; Cavaliere, Maria Luigia; Cerrato, Flavia; 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.
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
BamHI RFLP linked to the human urokinase gene 1-gen-1985 Sebastio, G; Riccio, Andrea; Verde, P; Scarpato, N; Blasi, F.
Beckwith-Wiedemann Syndrome 1-gen-2019 Mussa, A; Kalish, J; Cerrato, F; Riccio, A; Ferrero, Gb
Beckwith-Wiedemann syndrome and twinning: case report and brief review of literature 1-gen-2023 Elefante, Pierandrea; Spedicati, Beatrice; Faletra, Flavio; Pignata, Laura; Cerrato, Flavia; Riccio, Andrea; Barbi, Egidio; Memo, Luigi; Travan, Laura
Beckwith-Wiedemann syndrome. Clinical and etiopathogenic aspects of a model genomic imprinting entity 1-gen-2018 Cammarata-Scalisi, Francisco; Avendaño, Andrea; Stock, Frances; Callea, Michele; Sparago, Angela; Riccio, Andrea