Sfoglia per Autore
Performance Metrics of the Scoring System for the Diagnosis of the Beckwith-Wiedemann Spectrum (BWSp) and Its Correlation with Cancer Development
2023 Luca, Maria; Carli, Diana; Cardaropoli, Simona; Milani, Donatella; Cocchi, Guido; Leoni, Chiara; Macchiaiolo, Marina; Bartuli, Andrea; Tarani, Luigi; Melis, Daniela; Bontempo, Piera; D'Elia, Gemma; Prada, Elisabetta; Vitale, Raffaele; Grammegna, Angelina; Tannorella, Pierpaola; Sparago, Angela; Pignata, Laura; Riccio, Andrea; Russo, Silvia; Ferrero, Giovanni Battista; Mussa, Alessandro
Imprinting disorders
2023 Eggermann, Thomas; Monk, David; Perez de Nanclares, Guiomar; Kagami, Masayo; Giabicani, Eloïse; Riccio, Andrea; Tümer, Zeynep; Kalish, Jennifer M.; Tauber, Maithé; Duis, Jessica; Weksberg, Rosanna; Maher, Eamonn R.; Begemann, Matthias; Elbracht, Miriam
ICF1-Syndrome-Associated DNMT3B Mutations Prevent De Novo Methylation at a Subset of Imprinted Loci during iPSC Reprogramming
2023 Verma, A.; Poondi Krishnan, V.; Cecere, F.; D'Angelo, E.; Lullo, V.; Strazzullo, M.; Selig, S.; Angelini, C.; Matarazzo, M. R.; Riccio, A.
Co-Occurrence of Beckwith–Wiedemann Syndrome and Early-Onset Colorectal Cancer
2023 Cecere, F.; Pignata, L.; Hay Mele, B.; Saadat, A.; D'Angelo, E.; Palumbo, O.; Palumbo, P.; Carella, M.; Scarano, G.; Rossi, G. B.; Angelini, C.; Sparago, A.; Cerrato, F.; Riccio, A.
A maternal-effectPadi6variant causes nuclear and cytoplasmic abnormalities in oocytes, as well as failure of epigenetic reprogramming and zygotic genome activation in embryos
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
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Performance Metrics of the Scoring System for the Diagnosis of the Beckwith-Wiedemann Spectrum (BWSp) and Its Correlation with Cancer Development | 1-gen-2023 | Luca, Maria; Carli, Diana; Cardaropoli, Simona; Milani, Donatella; Cocchi, Guido; Leoni, Chiara; Macchiaiolo, Marina; Bartuli, Andrea; Tarani, Luigi; Melis, Daniela; Bontempo, Piera; D'Elia, Gemma; Prada, Elisabetta; Vitale, Raffaele; Grammegna, Angelina; Tannorella, Pierpaola; Sparago, Angela; Pignata, Laura; Riccio, Andrea; Russo, Silvia; Ferrero, Giovanni Battista; Mussa, Alessandro | |
| Imprinting disorders | 1-gen-2023 | Eggermann, Thomas; Monk, David; Perez de Nanclares, Guiomar; Kagami, Masayo; Giabicani, Eloïse; Riccio, Andrea; Tümer, Zeynep; Kalish, Jennifer M.; Tauber, Maithé; Duis, Jessica; Weksberg, Rosanna; Maher, Eamonn R.; Begemann, Matthias; Elbracht, Miriam | |
| ICF1-Syndrome-Associated DNMT3B Mutations Prevent De Novo Methylation at a Subset of Imprinted Loci during iPSC Reprogramming | 1-gen-2023 | Verma, A.; Poondi Krishnan, V.; Cecere, F.; D'Angelo, E.; Lullo, V.; Strazzullo, M.; Selig, S.; Angelini, C.; Matarazzo, M. R.; Riccio, A. | |
| Co-Occurrence of Beckwith–Wiedemann Syndrome and Early-Onset Colorectal Cancer | 1-gen-2023 | Cecere, F.; Pignata, L.; Hay Mele, B.; Saadat, A.; D'Angelo, E.; Palumbo, O.; Palumbo, P.; Carella, M.; Scarano, G.; Rossi, G. B.; Angelini, C.; Sparago, A.; Cerrato, F.; Riccio, A. | |
| 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 |
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