Search Results - Flavia Cerrato

  • Showing 1 - 15 results of 15
Refine Results
  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 by Manuela Priolo, Angela Sparago, Corrado Mammì, Flavia Cerrato, Carmelo Laganà, Andrea Riccio

    Published 2008
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  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 by Angela Sparago, Flavia Cerrato, Maria Vernucci, Giovanni Battista Ferrero, Margherita Silengo, Andrea Riccio

    Published 2004
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  3. 3
    Assisted Reproductive Techniques and Risk of Beckwith-Wiedemann Syndrome

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

    Published 2017
    Get full text
    Artigo
    Save to List
    Saved in:
  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 by 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

    Published 2008
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  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 by 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

    Published 2006
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  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... by 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

    Published 2008
    Get full text
    Artigo
    Save to List
    Saved in:
  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 by 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

    Published 2020
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  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 by 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

    Published 2015
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  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 by 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

    Published 2011
    Get full text
    Artigo
    Save to List
    Saved in:
  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... by 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

    Published 2024
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  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 by 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

    Published 2012
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  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 by 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

    Published 2008
    Get full text
    Artigo
    Save to List
    Saved in:
  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 by 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

    Published 2019
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  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 by 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

    Published 2008
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  15. 15
    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 by 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

    Published 2024
    Get full text
    Revisão
    Save to List
    Saved in:

Search Tools: