Sfoglia per Autore HAY MELE, Bruno
The mismatch-repair proteins MSH2 and MSH6 interact with the imprinting control regions through the ZFP57-KAP1 complex
2022 Acurzio, Basilia; Cecere, Francesco; Giaccari, Carlo; Verma, Ankit; Russo, Rosita; Valletta, Mariangela; Hay Mele, Bruno; Angelini, Claudia; Chambery, Angela; Riccio, Andrea
Novel genetic variants of KHDC3L and other members of the subcortical maternal complex associated with Beckwith-Wiedemann syndrome or Pseudohypoparathyroidism 1B and multi-locus imprinting disturbances
2022 Pignata, Laura; Cecere, Francesco; Verma, Ankit; Hay Mele, Bruno; Monticelli, Maria; Acurzio, Basilia; Giaccari, Carlo; Sparago, Angela; Hernandez Mora, Jose Ramon; Monteagudo-Sánchez, Ana; Esteller, Manel; Pereda, Arrate; Tenorio-Castano, Jair; Palumbo, Orazio; Carella, Massimo; Prontera, Paolo; Piscopo, Carmelo; Accadia, Maria; Lapunzina, Pablo; Cubellis, Maria Vittoria; de Nanclares, Guiomar Perez; Monk, David; Riccio, Andrea; Cerrato, Flavia
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 |
|---|---|---|---|
| The mismatch-repair proteins MSH2 and MSH6 interact with the imprinting control regions through the ZFP57-KAP1 complex | 1-gen-2022 | Acurzio, Basilia; Cecere, Francesco; Giaccari, Carlo; Verma, Ankit; Russo, Rosita; Valletta, Mariangela; Hay Mele, Bruno; Angelini, Claudia; Chambery, Angela; Riccio, Andrea | |
| Novel genetic variants of KHDC3L and other members of the subcortical maternal complex associated with Beckwith-Wiedemann syndrome or Pseudohypoparathyroidism 1B and multi-locus imprinting disturbances | 1-gen-2022 | Pignata, Laura; Cecere, Francesco; Verma, Ankit; Hay Mele, Bruno; Monticelli, Maria; Acurzio, Basilia; Giaccari, Carlo; Sparago, Angela; Hernandez Mora, Jose Ramon; Monteagudo-Sánchez, Ana; Esteller, Manel; Pereda, Arrate; Tenorio-Castano, Jair; Palumbo, Orazio; Carella, Massimo; Prontera, Paolo; Piscopo, Carmelo; Accadia, Maria; Lapunzina, Pablo; Cubellis, Maria Vittoria; de Nanclares, Guiomar Perez; Monk, David; Riccio, Andrea; Cerrato, Flavia | |
| 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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