CECERE, FRANCESCO
CECERE, FRANCESCO
Dipartimento di Scienze e Tecnologie Ambientali Biologiche e Farmaceutiche (DISTABiF)
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
A novel iPSC-based model of ICF syndrome subtype 2 recapitulates the molecular phenotype of ZBTB24 deficiency
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
Co-occurrence of Beckwith-Wiedemann syndrome and pseudohypoparathyroidism type 1B: coincidence or common molecular mechanism?
2023 Pignata, Laura; Cecere, Francesco; Acquaviva, Fabio; D'Angelo, Emilia; Cioffi, Daniela; Pellino, Valeria; Palumbo, Orazio; Palumbo, Pietro; Carella, Massimo; Sparago, Angela; De Brasi, Daniele; Cerrato, Flavia; Riccio, Andrea
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.
Different Mechanisms Cause Hypomethylation of Both H19 and KCNQ1OT1 Imprinted Differentially Methylated Regions in Two Cases of Silver-Russell Syndrome Spectrum
2022 Passaretti, Francesco; Pignata, Laura; Vitiello, Giuseppina; Alesi, Viola; D'Elia, Gemma; Cecere, Francesco; Acquaviva, Fabio; De Brasi, Daniele; Novelli, Antonio; Riccio, Andrea; Iolascon, Achille; Cerrato, Flavia
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.
New insights into oocyte cytoplasmic lattice-associated proteins
2024 Giaccari, Carlo; Cecere, Francesco; Argenziano, Lucia; Pagano, 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
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
The number of the CTCF binding sites of the H19/IGF2:IG-DMR correlates with DNA methylation and expression imprinting in a humanized mouse model
2021 Freschi, A.; Del Prete, R.; Pignata, L.; Cecere, F.; Manfrevola, F.; Mattia, M.; Cobellis, G.; Sparago, A.; Bartolomei, M. S.; Riccio, A.; Cerrato, F.
Zfp57 inactivation illustrates the role of ICR methylation in imprinted gene expression during neural differentiation of mouse ESCs
2021 Acurzio, B.; Verma, A.; Polito, A.; Giaccari, C.; Cecere, F.; Fioriniello, S.; Della Ragione, F.; Fico, A.; Cerrato, F.; Angelini, C.; Feil, R.; Riccio, A.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| 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 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 | |
| Co-occurrence of Beckwith-Wiedemann syndrome and pseudohypoparathyroidism type 1B: coincidence or common molecular mechanism? | 1-gen-2023 | Pignata, Laura; Cecere, Francesco; Acquaviva, Fabio; D'Angelo, Emilia; Cioffi, Daniela; Pellino, Valeria; Palumbo, Orazio; Palumbo, Pietro; Carella, Massimo; Sparago, Angela; De Brasi, Daniele; Cerrato, Flavia; Riccio, Andrea | |
| 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. | |
| Different Mechanisms Cause Hypomethylation of Both H19 and KCNQ1OT1 Imprinted Differentially Methylated Regions in Two Cases of Silver-Russell Syndrome Spectrum | 1-gen-2022 | Passaretti, Francesco; Pignata, Laura; Vitiello, Giuseppina; Alesi, Viola; D'Elia, Gemma; Cecere, Francesco; Acquaviva, Fabio; De Brasi, Daniele; Novelli, Antonio; Riccio, Andrea; Iolascon, Achille; Cerrato, Flavia | |
| 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. | |
| New insights into oocyte cytoplasmic lattice-associated proteins | 1-gen-2024 | Giaccari, Carlo; Cecere, Francesco; Argenziano, Lucia; Pagano, 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 | |
| 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 | |
| The number of the CTCF binding sites of the H19/IGF2:IG-DMR correlates with DNA methylation and expression imprinting in a humanized mouse model | 1-gen-2021 | Freschi, A.; Del Prete, R.; Pignata, L.; Cecere, F.; Manfrevola, F.; Mattia, M.; Cobellis, G.; Sparago, A.; Bartolomei, M. S.; Riccio, A.; Cerrato, F. | |
| Zfp57 inactivation illustrates the role of ICR methylation in imprinted gene expression during neural differentiation of mouse ESCs | 1-gen-2021 | Acurzio, B.; Verma, A.; Polito, A.; Giaccari, C.; Cecere, F.; Fioriniello, S.; Della Ragione, F.; Fico, A.; Cerrato, F.; Angelini, C.; Feil, R.; Riccio, A. |