Transcriptional Reactivation of the FMR1 Gene. A Possible Approach to the Treatment of the Fragile X Syndrome

by Elisabetta Tabolacci, Federica Palumbo, Veronica Nobile, Giovanni Neri
Published 2016-08-01

DNA Methylation, Mechanisms of <i>FMR1</i> Inactivation and Therapeutic Perspectives for Fragile X Syndrome

by Veronica Nobile, Cecilia Pucci, Pietro Chiurazzi, Giovanni Neri, Elisabetta Tabolacci
Published 2021-02-01

Role of CTCF protein in regulating FMR1 locus transcription.

by Stella Lanni, Martina Goracci, Loredana Borrelli, Giorgia Mancano, Pietro Chiurazzi, Umberto Moscato, Fabrizio Ferrè, Manuela Helmer-Citterich, Elisabetta Tabolacci, Giovanni Neri
Published 2013-01-01

Reversion to Normal of <i>FMR1</i> Expanded Alleles: A Rare Event in Two Independent Fragile X Syndrome Families

by Elisabetta Tabolacci, Roberta Pietrobono, Giulia Maneri, Laura Remondini, Veronica Nobile, Matteo Della Monica, Maria Grazia Pomponi, Maurizio Genuardi, Giovanni Neri, Pietro Chiurazzi
Published 2020-02-01

Tumorigenic potential of olfactory bulb-derived human adult neural stem cells associates with activation of TERT and NOTCH1.

by Patrizia Casalbore, Manuela Budoni, Lucia Ricci-Vitiani, Carlo Cenciarelli, Giovanna Petrucci, Luisa Milazzo, Nicola Montano, Elisabetta Tabolacci, Giulio Maira, Luigi M Larocca, Roberto Pallini
Published 2009-01-01

DNA Methylation in the Diagnosis of Monogenic Diseases

by 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 M Sirchia, Gabriella Maria Squeo, Silvia Tabano, Elisabetta Tabolacci, Isabella Torrente, Maurizio Genuardi, Giovanni Neri, Andrea Riccio
Published 2020-03-01