نتائج البحث - Flavia Cerrato

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  1. 1
    MS-MLPA is a specific and sensitive technique for detecting all chromosome 11p15.5 imprinting defects of BWS and SRS in a single-tube experiment

    MS-MLPA is a specific and sensitive technique for detecting all chromosome 11p15.5 imprinting defects of BWS and SRS in a single-tube experiment حسب Manuela Priolo, Angela Sparago, Corrado Mammì, Flavia Cerrato, Carmelo Laganà, Andrea Riccio

    منشور في 2008
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  2. 2
    Microdeletions in the human H19 DMR result in loss of IGF2 imprinting and Beckwith-Wiedemann syndrome

    Microdeletions in the human H19 DMR result in loss of IGF2 imprinting and Beckwith-Wiedemann syndrome حسب Angela Sparago, Flavia Cerrato, Maria Vernucci, Giovanni Battista Ferrero, Margherita Silengo, Andrea Riccio

    منشور في 2004
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  3. 3
    Assisted Reproductive Techniques and Risk of Beckwith-Wiedemann Syndrome

    Assisted Reproductive Techniques and Risk of Beckwith-Wiedemann Syndrome حسب Alessandro Mussa, Cristina Molinatto, Flavia Cerrato, Orazio Palumbo, Massimo Carella, Giuseppina Baldassarre, Diana Carli, Clementina Peris, Andrea Riccio, Giovanni Battista Ferrero

    منشور في 2017
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  4. 4
    Distinct Methylation Changes at the IGF2-H19 Locus in Congenital Growth Disorders and Cancer

    Distinct Methylation Changes at the IGF2-H19 Locus in Congenital Growth Disorders and Cancer حسب Adele Murrell, Yoko Itō, Gaetano Verde, Joanna E. Huddleston, Kathryn Woodfine, Margherita Silengo, Filippo Spreafico, Daniela Perotti, Agostina De Crescenzo, Angela Sparago, Flavia Cerrato, Andrea Riccio

    منشور في 2008
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  5. 5
    Mechanisms causing imprinting defects in familial Beckwith–Wiedemann syndrome with Wilms' tumour

    Mechanisms causing imprinting defects in familial Beckwith–Wiedemann syndrome with Wilms' tumour حسب Angela Sparago, Silvia Russo, Flavia Cerrato, Serena Ferraiuolo, Pierangela Castorina, Angelo Selicorni, Christine Schwienbacher, Massimo Negrini, Giovanni Battista Ferrero, Margherita Silengo, Cecilia Anichini, Lidia Larizza, Andrea Riccio

    منشور في 2006
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  6. 6
    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

    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 mutatio... حسب Roberto Rosati, Flavia Cerrato, Mabrouka Doghman, Mara Albonei Dudeque Pianovski, Guilherme A. Parise, Gislaine Custódio, Gerard P. Zambetti, Raul C. Ribeiro, Andrea Riccio, Bonald C. Figueiredo, Enzo Lalli

    منشور في 2008
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  7. 7
    Loss-of-function maternal-effect mutations of PADI6 are associated with familial and sporadic Beckwith-Wiedemann syndrome with multi-locus imprinting disturbance

    Loss-of-function maternal-effect mutations of PADI6 are associated with familial and sporadic Beckwith-Wiedemann syndrome with multi-locus imprinting disturbance حسب Maria Vittoria Cubellis, Laura Pignata, Ankit Verma, Angela Sparago, Rosita Del Prete, Maria Monticelli, Luciano Calzari, Vincenzo Antona, Daniela Melis, Romano Tenconi, Silvia Russo, Flavia Cerrato, Andrea Riccio

    منشور في 2020
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  8. 8
    ZFP57 recognizes multiple and closely spaced sequence motif variants to maintain repressive epigenetic marks in mouse embryonic stem cells

    ZFP57 recognizes multiple and closely spaced sequence motif variants to maintain repressive epigenetic marks in mouse embryonic stem cells حسب Zahra Anvar, M Cammisa, Vincenzo Riso, Ilaria Baglivo, Harpreet Kukreja, Angela Sparago, Michael Girardot, Shraddha Lad, Italia De Feis, Flavia Cerrato, Claudia Angelini, Robert Feil, Paolo V. Pedone, Giovanna Grimaldi, Andrea Riccio

    منشور في 2015
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  9. 9
    The KCNQ1OT1 imprinting control region and non-coding RNA: new properties derived from the study of Beckwith–Wiedemann syndrome and Silver–Russell syndrome cases

    The KCNQ1OT1 imprinting control region and non-coding RNA: new properties derived from the study of Beckwith–Wiedemann syndrome and Silver–Russell syndrome cases حسب Nicoletta Chiesa, Agostina De Crescenzo, Kankadeb Mishra, Lucia Perone, Massimo Carella, Orazio Palumbo, Alessandro Mussa, Angela Sparago, Flavia Cerrato, Silvia Russo, Elisabetta Lapi, Maria Vittoria Cubellis, Chandrasekhar Kanduri, Margherita Silengo, Andrea Riccio, Giovanni Battista Ferrero

    منشور في 2011
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  10. 10
    A maternal-effect<i>Padi6</i>variant causes nuclear and cytoplasmic abnormalities in oocytes, as well as failure of epigenetic reprogramming and zygotic genome activation in embryos

    A maternal-effect<i>Padi6</i>variant causes nuclear and cytoplasmic abnormalities in oocytes, as well as failure of epigenetic reprogramming and zygotic genome activation in embryo... حسب Carlo Giaccari, Francesco Cecere, Lucia Argenziano, Angela Pagano, António Galvão, Dario Acampora, Gianna Rossi, Bruno Hay Mele, Basilia Acurzio, Scott A. Coonrod, Maria Vittoria Cubellis, Flavia Cerrato, Simon Andrews, Sandra Cecconi, Gavin Kelsey, Andrea Riccio

    منشور في 2024
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  11. 11
    The molecular function and clinical phenotype of partial deletions of the IGF2/H19 imprinting control region depends on the spatial arrangement of the remaining CTCF-binding sites

    The molecular function and clinical phenotype of partial deletions of the IGF2/H19 imprinting control region depends on the spatial arrangement of the remaining CTCF-binding sites حسب Jasmin Beygo, Valentina Citro, Angela Sparago, Agostina De Crescenzo, Flavia Cerrato, Melanie Heitmann, Katrin Rademacher, Andrea Guala, Thorsten Enklaar, Cecilia Anichini, Margherita Silengo, Notker Graf, Dirk Prawitt, Maria Vittoria Cubellis, Bernhard Horsthemke, Karin Buiting, Andrea Riccio

    منشور في 2012
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  12. 12
    Different mechanisms cause imprinting defects at the IGF2/H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumour

    Different mechanisms cause imprinting defects at the IGF2/H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumour حسب Flavia Cerrato, Angela Sparago, Gaetano Verde, Agostina De Crescenzo, Valentina Citro, Maria Vittoria Cubellis, M M Rinaldi, Luigi Boccuto, Giampiero Neri, Corrado Magnani, Paolo D’Angelo, Paola Collini, Daniela Perotti, Gianfranco Sebastio, Eamonn R. Maher, Andrea Riccio

    منشور في 2008
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  13. 13
    Transcription alterations of KCNQ1 associated with imprinted methylation defects in the Beckwith–Wiedemann locus

    Transcription alterations of KCNQ1 associated with imprinted methylation defects in the Beckwith–Wiedemann locus حسب Federica Maria Valente, Angela Sparago, Andrea Freschi, Katherine L Hill-Harfe, Saskia M. Maas, Suzanna G.M. Frints, Mariëlle Alders, Laura Pignata, Monica Franzese, Claudia Angelini, Diana Carli, Alessandro Mussa, Andrea Gazzin, Fulvio Gabbarini, Basilia Acurzio, Giovanni Battista Ferrero, Jet Bliek, Charles A. Williams, Andrea Riccio, Flavia Cerrato

    منشور في 2019
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  14. 14
    Hypomethylation at multiple maternally methylated imprinted regions including PLAGL1 and GNAS loci in Beckwith–Wiedemann syndrome

    Hypomethylation at multiple maternally methylated imprinted regions including PLAGL1 and GNAS loci in Beckwith–Wiedemann syndrome حسب Jet Bliek, Gaetano Verde, Jonathan L A Callaway, Saskia M. Maas, Agostina De Crescenzo, Angela Sparago, Flavia Cerrato, Silvia Russo, Serena Ferraiuolo, Maria Michela Rinaldi, Rita Fischetto, Faustina Lalatta, Lucio Giordano, Paola Ferrari, Maria Vittoria Cubellis, Lidia Larizza, I. Karen Temple, Marcel M.A.M. Mannens, Deborah Mackay, Andrea Riccio

    منشور في 2008
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  15. 15
    DNA Methylation in the Diagnosis of Monogenic Diseases

    DNA Methylation in the Diagnosis of Monogenic Diseases حسب Flavia Cerrato, Angela Sparago, Francesca Ariani, Fulvia Brugnoletti, Luciano Calzari, Fabio Coppedè, Alessandro De Luca, Cristina Gervasini, Emiliano Giardina, Fiorella Gurrieri, Cristiana Lo Nigro, Giuseppe Merla, Monica Miozzo, Silvia Russo, Eugenio Sangiorgi, Silvia Maria Sirchia, Gabriella Maria Squeo, Silvia Tabano, Elisabetta Tabolacci, Isabella Torrente, Maurizio Genuardi, Giovanni Neri, Andrea Riccio

    منشور في 2020
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  16. 16
    Multi-locus imprinting disturbance (MLID): interim joint statement for clinical and molecular diagnosis

    Multi-locus imprinting disturbance (MLID): interim joint statement for clinical and molecular diagnosis حسب Deborah Mackay, Gabriella Gazdagh, David Monk, Frédéric Brioude, Éloïse Giabicani, I. Krzyzewska, Jennifer M. Kalish, Saskia M. Maas, Masayo Kagami, Jasmin Beygo, Tiina Kahre, Jair Tenorio, Laima Ambrozaitytė, Birutė Burnytė, Flavia Cerrato, Justin H. Davies, Giovanni Battista Ferrero, Olga Fjodorova, África Manero-Azua, Arrate Pereda, Silvia Russo, Pierpaola Tannorella, I. Karen Temple, Katrin Õunap, Andrea Riccio, Guiomar Pérez de Nanclares, Eamonn R. Maher, Pablo Lapunzina, Irène Netchine, Thomas Eggermann, Jet Bliek, Zeynep Tümer

    منشور في 2024
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