Showing 1 - 7 results of 7 for search 'Francesco Cecere', query time: 0.03s Refine Results
  1. 1
    The mismatch-repair proteins MSH2 and MSH6 interact with the imprinting control regions through the ZFP57-KAP1 complex

    The mismatch-repair proteins MSH2 and MSH6 interact with the imprinting control regions through the ZFP57-KAP1 complex by Basilia Acurzio, Francesco Cecere, Carlo Giaccari, Ankit Verma, Rosita Russo, Mariangela Valletta, Bruno Hay Mele, Claudia Angelini, Angela Chambery, Andrea Riccio

    Published 2022-08-01
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  2. 2
    ICF1-Syndrome-Associated <i>DNMT3B</i> Mutations Prevent De Novo Methylation at a Subset of Imprinted Loci during iPSC Reprogramming

    ICF1-Syndrome-Associated <i>DNMT3B</i> Mutations Prevent De Novo Methylation at a Subset of Imprinted Loci during iPSC Reprogramming by Ankit Verma, Varsha Poondi Krishnan, Francesco Cecere, Emilia D’Angelo, Vincenzo Lullo, Maria Strazzullo, Sara Selig, Claudia Angelini, Maria R. Matarazzo, Andrea Riccio

    Published 2023-11-01
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  3. 3
    Zfp57 inactivation illustrates the role of ICR methylation in imprinted gene expression during neural differentiation of mouse ESCs

    Zfp57 inactivation illustrates the role of ICR methylation in imprinted gene expression during neural differentiation of mouse ESCs by Basilia Acurzio, Ankit Verma, Alessia Polito, Carlo Giaccari, Francesco Cecere, Salvatore Fioriniello, Floriana Della Ragione, Annalisa Fico, Flavia Cerrato, Claudia Angelini, Robert Feil, Andrea Riccio

    Published 2021-07-01
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  4. 4
    Different Mechanisms Cause Hypomethylation of Both <i>H19</i> and <i>KCNQ1OT1</i> Imprinted Differentially Methylated Regions in Two Cases of Silver–Russell Syndrome Spectrum

    Different Mechanisms Cause Hypomethylation of Both <i>H19</i> and <i>KCNQ1OT1</i> Imprinted Differentially Methylated Regions in Two Cases of Silver–Russell Syndrome Spectrum by Francesco Passaretti, Laura Pignata, Giuseppina Vitiello, Viola Alesi, Gemma D’Elia, Francesco Cecere, Fabio Acquaviva, Daniele De Brasi, Antonio Novelli, Andrea Riccio, Achille Iolascon, Flavia Cerrato

    Published 2022-10-01
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  5. 5
    Co-occurrence of Beckwith-Wiedemann syndrome and pseudohypoparathyroidism type 1B: coincidence or common molecular mechanism?

    Co-occurrence of Beckwith-Wiedemann syndrome and pseudohypoparathyroidism type 1B: coincidence or common molecular mechanism? by Laura Pignata, Francesco Cecere, Fabio Acquaviva, Emilia D’Angelo, Daniela Cioffi, Valeria Pellino, Orazio Palumbo, Pietro Palumbo, Massimo Carella, Angela Sparago, Daniele De Brasi, Flavia Cerrato, Andrea Riccio, Andrea Riccio

    Published 2023-08-01
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  6. 6
    Co-Occurrence of Beckwith–Wiedemann Syndrome and Early-Onset Colorectal Cancer

    Co-Occurrence of Beckwith–Wiedemann Syndrome and Early-Onset Colorectal Cancer by Francesco Cecere, Laura Pignata, Bruno Hay Mele, Abu Saadat, Emilia D’Angelo, Orazio Palumbo, Pietro Palumbo, Massimo Carella, Gioacchino Scarano, Giovanni Battista Rossi, Claudia Angelini, Angela Sparago, Flavia Cerrato, Andrea Riccio

    Published 2023-03-01
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  7. 7
    Understanding the Variability of 22q11.2 Deletion Syndrome: The Role of Epigenetic Factors

    Understanding the Variability of 22q11.2 Deletion Syndrome: The Role of Epigenetic Factors by Francesca Cillo, Emma Coppola, Federico Habetswallner, Francesco Cecere, Laura Pignata, Elisabetta Toriello, Antonio De Rosa, Laura Grilli, Antonio Ammendola, Paolo Salerno, Roberta Romano, Emilia Cirillo, Giuseppe Merla, Andrea Riccio, Claudio Pignata, Giuliana Giardino

    Published 2024-02-01
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