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

por Tabolacci, Elisabetta, Palumbo, Federica, Nobile, Veronica, Neri, Giovanni
Publicado 2016

Mechanisms of the FMR1 Repeat Instability: How Does the CGG Sequence Expand?

por Tabolacci, Elisabetta, Nobile, Veronica, Pucci, Cecilia, Chiurazzi, Pietro
Publicado 2022

DNA Methylation, Mechanisms of FMR1 Inactivation and Therapeutic Perspectives for Fragile X Syndrome

por Nobile, Veronica, Pucci, Cecilia, Chiurazzi, Pietro, Neri, Giovanni, Tabolacci, Elisabetta
Publicado 2021

The mGluR5 antagonist AFQ056 does not affect methylation and transcription of the mutant FMR1 gene in vitro

por Tabolacci, Elisabetta, Pirozzi, Filomena, Gomez-Mancilla, Baltazar, Gasparini, Fabrizio, Neri, Giovanni
Publicado 2012

Remifentanil does not affect human microglial immune activation in response to pro-inflammatory cytokines

por Dello Russo, Cinzia, Cappoli, Natalia, Tabolacci, Elisabetta, Sollazzi, Liliana, Navarra, Pierluigi, Aceto, Paola
Publicado 2023

RADX Gene Variant May Predispose to Familial Asperger Syndrome

por Azzarà, Alessia, Rumore, Roberto, Brugnoletti, Fulvia, Tabolacci, Elisabetta, Bottillo, Irene, Sangiorgi, Eugenio, Gurrieri, Fiorella
Publicado 2023

Rutin Protects Fibroblasts from UVA Radiation through Stimulation of Nrf2 Pathway

por Tabolacci, Elisabetta, Tringali, Giuseppe, Nobile, Veronica, Duca, Sara, Pizzoferrato, Michela, Bottoni, Patrizia, Maria Elisabetta, Clementi
Publicado 2023

The mTOR kinase inhibitor rapamycin enhances the expression and release of pro-inflammatory cytokine interleukin 6 modulating the activation of human microglial cells

por Cappoli, Natalia, Mezzogori, Daniele, Tabolacci, Elisabetta, Coletta, Isabella, Navarra, Pierluigi, Pani, Giovambattista, Dello Russo, Cinzia
Publicado 2019

Genome-wide methylation analysis demonstrates that 5-aza-2-deoxycytidine treatment does not cause random DNA demethylation in fragile X syndrome cells

por Tabolacci, Elisabetta, Mancano, Giorgia, Lanni, Stella, Palumbo, Federica, Goracci, Martina, Ferrè, Fabrizio, Helmer-Citterich, Manuela, Neri, Giovanni
Publicado 2016

Role of CTCF Protein in Regulating FMR1 Locus Transcription

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

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

por Tabolacci, Elisabetta, Pietrobono, Roberta, Maneri, Giulia, Remondini, Laura, Nobile, Veronica, Della Monica, Matteo, Pomponi, Maria Grazia, Genuardi, Maurizio, Neri, Giovanni, Chiurazzi, Pietro
Publicado 2020

Age-Dependent Dysregulation of APP in Neuronal and Skin Cells from Fragile X Individuals

por Cencelli, Giulia, Pacini, Laura, De Luca, Anastasia, Messia, Ilenia, Gentile, Antonietta, Kang, Yunhee, Nobile, Veronica, Tabolacci, Elisabetta, Jin, Peng, Farace, Maria Giulia, Bagni, Claudia
Publicado 2023

Tumorigenic Potential of Olfactory Bulb-Derived Human Adult Neural Stem Cells Associates with Activation of TERT and NOTCH1

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

Co-Occurrence of Fragile X Syndrome with a Second Genetic Condition: Three Independent Cases of Double Diagnosis

por Tabolacci, Elisabetta, Pomponi, Maria Grazia, Remondini, Laura, Pietrobono, Roberta, Orteschi, Daniela, Nobile, Veronica, Pucci, Cecilia, Musto, Elisa, Pane, Marika, Mercuri, Eugenio M., Neri, Giovanni, Genuardi, Maurizio, Chiurazzi, Pietro, Zollino, Marcella
Publicado 2021

Mother and Daughter Carrying of the Same Pathogenic Variant in FGFR2 with Discordant Phenotype

por Lo Vecchio, Filomena, Tabolacci, Elisabetta, Nobile, Veronica, Pomponi, Maria Grazia, Pietrobono, Roberta, Neri, Giovanni, Amenta, Simona, Candida, Ettore, Grippaudo, Cristina, Lo Cascio, Ettore, Vita, Alessia, Tiberio, Federica, Arcovito, Alessandro, Lattanzi, Wanda, Genuardi, Maurizio, Chiurazzi, Pietro
Publicado 2022

DNA Methylation in the Diagnosis of Monogenic Diseases

por Cerrato, Flavia, Sparago, Angela, Ariani, Francesca, Brugnoletti, Fulvia, Calzari, Luciano, Coppedè, Fabio, De Luca, Alessandro, Gervasini, Cristina, Giardina, Emiliano, Gurrieri, Fiorella, Lo Nigro, Cristiana, Merla, Giuseppe, Miozzo, Monica, Russo, Silvia, Sangiorgi, Eugenio, Sirchia, Silvia M, Squeo, Gabriella Maria, Tabano, Silvia, Tabolacci, Elisabetta, Torrente, Isabella, Genuardi, Maurizio, Neri, Giovanni, Riccio, Andrea
Publicado 2020

CGG Repeat-Induced FMR1 Silencing Depends on the Expansion Size in Human iPSCs and Neurons Carrying Unmethylated Full Mutations

por Brykczynska, Urszula, Pecho-Vrieseling, Eline, Thiemeyer, Anke, Klein, Jessica, Fruh, Isabelle, Doll, Thierry, Manneville, Carole, Fuchs, Sascha, Iazeolla, Mariavittoria, Beibel, Martin, Roma, Guglielmo, Naumann, Ulrike, Kelley, Nicholas, Oakeley, Edward J., Mueller, Matthias, Gomez-Mancilla, Baltazar, Bühler, Marc, Tabolacci, Elisabetta, Chiurazzi, Pietro, Neri, Giovanni, Bouwmeester, Tewis, Di Giorgio, Francesco Paolo, Fodor, Barna D.
Publicado 2016