Tabolacci, Elisabetta
Tabolacci, Elisabetta
ROMA - Dipartimento di Scienze della vita e sanità pubblica
Age-Dependent Dysregulation of APP in Neuronal and Skin Cells from Fragile X Individuals
2023 Cencelli, G; Pacini, L; De Luca, A; Messia, I; Gentile, A; Kang, Y; Nobile, Veronica; Tabolacci, Elisabetta; Jin, P; Farace, Mg; Bagni, C.
RADX Gene Variant May Predispose to Familial Asperger Syndrome
2023 Azzarà, Alessia; Rumore, Roberto; Brugnoletti, Fulvia; Tabolacci, Elisabetta; Bottillo, Irene; Sangiorgi, Eugenio; Gurrieri, Fiorella
REMIFENTANIL DOES NOT AFFECT HUMAN MICROGLIAL IMMUNE ACTIVATION IN RESPONSE TO PRO-INFLAMMATORY CYTOKINES
2023 Dello Russo, Cinzia; Cappoli, Natalia; Tabolacci, Elisabetta; Sollazzi, Liliana; Navarra, Pierluigi; Aceto, Paola
Rutin Protects Fibroblasts from UVA Radiation through Stimulation of Nrf2 Pathway.
2023 Tabolacci, Elisabetta; Tringali, Giuseppe; Nobile, Veronica; Duca, Sara; Pizzoferrato, Michela; Bottoni, Patrizia; Clementi, Maria Elisabetta
Mechanisms of the FMR1 Repeat Instability: How Does the CGG Sequence Expand?
2022 Tabolacci, Elisabetta; Nobile, Veronica; Pucci, Cecilia; Chiurazzi, Pietro
Mother and Daughter Carrying of the Same Pathogenic Variant in FGFR2 with Discordant Phenotype
2022 Lo Vecchio, F.; Tabolacci, E.; Nobile, V.; Pomponi, M. G.; Pietrobono, R.; Neri, G.; Amenta, S.; Candida, E.; Grippaudo, C.; Lo Cascio, E.; Vita, A.; Tiberio, F.; Arcovito, A.; Lattanzi, W.; Genuardi, M.; Chiurazzi, P.
Co-occurrence of fragile x syndrome with a second genetic condition: Three independent cases of double diagnosis
2021 Tabolacci, Elisabetta; Pomponi, M. G.; Remondini, L.; Pietrobono, R.; Orteschi, D.; Nobile, Veronica; Pucci, Cecilia; Musto, Elisa; Pane, Marika; Mercuri, Eugenio Maria; Neri, G.; Genuardi, Maurizio; Chiurazzi, Pietro; Zollino, Marcella
DNA Methylation, Mechanisms of FMR1 Inactivation and Therapeutic Perspectives for Fragile X Syndrome
2021 Nobile, Veronica; Pucci, Cecilia; Chiurazzi, Pietro; Neri, Giovanni; Tabolacci, Elisabetta
Effects of remifentanil on human C20 microglial pro-inflammatory activation
2021 Cappoli, N.; Aceto, P.; Tabolacci, E.; Mezzogori, D.; Sollazzi, L.; Navarra, P.; Dello Russo, C.
Infantile Liver Failure Syndrome 1 associated with a novel variant of the LARS1 gene: Clinical, genetic, and functional characterization
2021 Tabolacci, Elisabetta; Molinario, C; Marangi, Giuseppe; Nobile, Veronica; Arena, Vincenzo; Mendes, Mi; Smith, Dec; Salomons, Gs; Tana, Milena; Costa, S; Vento, Giovanni; Genuardi, Maurizio
Altered mitochondrial function in cells carrying a premutation or unmethylated full mutation of the FMR1 gene
2020 Nobile, V.; Palumbo, F.; Lanni, S.; Ghisio, V.; Vitali, A.; Castagnola, M.; Marzano, V.; Maulucci, G.; De Angelis, C.; De Spirito, M.; Pacini, L.; D'Andrea, L.; Ragno, R.; Stazi, G.; Valente, S.; Mai, A.; Chiurazzi, P.; Genuardi, M.; Neri, G.; Tabolacci, E.
DNA Methylation in the Diagnosis of Monogenic Diseases.
2020 Cerrato, F; Sparago, A; Ariani, F; Brugnoletti, F; Calzari, L; Coppedè, F; De Luca, A; Gervasini, C; Giardina, E; Gurrieri, F; Lo Nigro, C; Merla, G; Miozzo, M; Russo, S; Sangiorgi, E; Sirchia, Sm; Squeo, Gm; Tabano, S; Tabolacci, E; Torrente, I; Genuardi, M; Neri, G; Riccio, A.
Reversion to Normal of FMR1 Expanded Alleles: A Rare Event in Two Independent Fragile X Syndrome Families
2020 Tabolacci, Elisabetta; Pietrobono, Roberta; Maneri, Giulia; Remondini, Laura; Nobile, Veronica; Della Monica, Matteo; Pomponi, Maria Grazia; Genuardi, Maurizio; Neri, Giovanni; Chiurazzi, Pietro
The emerging role of the BDNF-TrkB signaling pathway in the modulation of pain perception
2020 Cappoli, N.; Tabolacci, E.; Aceto, P.; Dello Russo, C.
Methylated premutation of the FMR1 gene in three sisters: correlating CGG expansion and epigenetic inactivation
2020 Tabolacci, E.; Pomponi, M. G.; Remondini, L.; Pietrobono, R.; Nobile, V.; Pennacchio, G.; Gurrieri, F.; Neri, G.; Genuardi, M.; Chiurazzi, P.
The mTOR kinase inhibitor rapamycin enhances the expression and release of pro-inflammatory cytokine interleukin 6 modulating the activation of human microglial cells.
2019 Cappoli, N; Mezzogori, D; Tabolacci, E; Coletta, I; Navarra, P; Pani, G; Dello Russo, C.
Simpson–Golabi–Behmel syndrome in a female: A case report and an unsolved issue
2017 Vaisfeld, Alessandro; Pomponi, Maria Grazia; Pietrobono, Roberta; Tabolacci, Elisabetta; Neri, Giovanni
CGG Repeat-Induced FMR1 Silencing Depends on the Expansion Size in Human iPSCs and Neurons Carrying Unmethylated Full Mutations
2016 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.
Defining the role of the CGGBP1 protein in FMR1 gene expression
2016 Goracci, Martina; Lanni, Stella; Mancano, Giorgia; Palumbo, Federica; Chiurazzi, Pietro; Neri, Giovanni; Tabolacci, Elisabetta
Genome-wide methylation analysis demonstrates that 5-aza-2-deoxycytidine treatment does not cause random DNA demethylation in fragile X syndrome cells
2016 Tabolacci, Elisabetta; Mancano, Giorgia; Lanni, Stella; Palumbo, Federica; Goracci, Martina; Ferrè, Fabrizio; Helmer Citterich, Manuela; Neri, Giovanni
Data di pubblicazione | Titolo | Autore(i) | File |
---|---|---|---|
1-gen-2023 | Age-Dependent Dysregulation of APP in Neuronal and Skin Cells from Fragile X Individuals | Cencelli, G; Pacini, L; De Luca, A; Messia, I; Gentile, A; Kang, Y; Nobile, Veronica; Tabolacci, Elisabetta; Jin, P; Farace, Mg; Bagni, C. | |
1-gen-2023 | RADX Gene Variant May Predispose to Familial Asperger Syndrome | Azzarà, Alessia; Rumore, Roberto; Brugnoletti, Fulvia; Tabolacci, Elisabetta; Bottillo, Irene; Sangiorgi, Eugenio; Gurrieri, Fiorella | |
1-gen-2023 | REMIFENTANIL DOES NOT AFFECT HUMAN MICROGLIAL IMMUNE ACTIVATION IN RESPONSE TO PRO-INFLAMMATORY CYTOKINES | Dello Russo, Cinzia; Cappoli, Natalia; Tabolacci, Elisabetta; Sollazzi, Liliana; Navarra, Pierluigi; Aceto, Paola | |
1-gen-2023 | Rutin Protects Fibroblasts from UVA Radiation through Stimulation of Nrf2 Pathway. | Tabolacci, Elisabetta; Tringali, Giuseppe; Nobile, Veronica; Duca, Sara; Pizzoferrato, Michela; Bottoni, Patrizia; Clementi, Maria Elisabetta | |
1-gen-2022 | Mechanisms of the FMR1 Repeat Instability: How Does the CGG Sequence Expand? | Tabolacci, Elisabetta; Nobile, Veronica; Pucci, Cecilia; Chiurazzi, Pietro | |
1-gen-2022 | Mother and Daughter Carrying of the Same Pathogenic Variant in FGFR2 with Discordant Phenotype | Lo Vecchio, F.; Tabolacci, E.; Nobile, V.; Pomponi, M. G.; Pietrobono, R.; Neri, G.; Amenta, S.; Candida, E.; Grippaudo, C.; Lo Cascio, E.; Vita, A.; Tiberio, F.; Arcovito, A.; Lattanzi, W.; Genuardi, M.; Chiurazzi, P. | |
1-gen-2021 | Co-occurrence of fragile x syndrome with a second genetic condition: Three independent cases of double diagnosis | Tabolacci, Elisabetta; Pomponi, M. G.; Remondini, L.; Pietrobono, R.; Orteschi, D.; Nobile, Veronica; Pucci, Cecilia; Musto, Elisa; Pane, Marika; Mercuri, Eugenio Maria; Neri, G.; Genuardi, Maurizio; Chiurazzi, Pietro; Zollino, Marcella | |
1-gen-2021 | DNA Methylation, Mechanisms of FMR1 Inactivation and Therapeutic Perspectives for Fragile X Syndrome | Nobile, Veronica; Pucci, Cecilia; Chiurazzi, Pietro; Neri, Giovanni; Tabolacci, Elisabetta | |
1-gen-2021 | Effects of remifentanil on human C20 microglial pro-inflammatory activation | Cappoli, N.; Aceto, P.; Tabolacci, E.; Mezzogori, D.; Sollazzi, L.; Navarra, P.; Dello Russo, C. | |
1-gen-2021 | Infantile Liver Failure Syndrome 1 associated with a novel variant of the LARS1 gene: Clinical, genetic, and functional characterization | Tabolacci, Elisabetta; Molinario, C; Marangi, Giuseppe; Nobile, Veronica; Arena, Vincenzo; Mendes, Mi; Smith, Dec; Salomons, Gs; Tana, Milena; Costa, S; Vento, Giovanni; Genuardi, Maurizio | |
1-gen-2020 | Altered mitochondrial function in cells carrying a premutation or unmethylated full mutation of the FMR1 gene | Nobile, V.; Palumbo, F.; Lanni, S.; Ghisio, V.; Vitali, A.; Castagnola, M.; Marzano, V.; Maulucci, G.; De Angelis, C.; De Spirito, M.; Pacini, L.; D'Andrea, L.; Ragno, R.; Stazi, G.; Valente, S.; Mai, A.; Chiurazzi, P.; Genuardi, M.; Neri, G.; Tabolacci, E. | |
1-gen-2020 | DNA Methylation in the Diagnosis of Monogenic Diseases. | Cerrato, F; Sparago, A; Ariani, F; Brugnoletti, F; Calzari, L; Coppedè, F; De Luca, A; Gervasini, C; Giardina, E; Gurrieri, F; Lo Nigro, C; Merla, G; Miozzo, M; Russo, S; Sangiorgi, E; Sirchia, Sm; Squeo, Gm; Tabano, S; Tabolacci, E; Torrente, I; Genuardi, M; Neri, G; Riccio, A. | |
1-gen-2020 | Reversion to Normal of FMR1 Expanded Alleles: A Rare Event in Two Independent Fragile X Syndrome Families | Tabolacci, Elisabetta; Pietrobono, Roberta; Maneri, Giulia; Remondini, Laura; Nobile, Veronica; Della Monica, Matteo; Pomponi, Maria Grazia; Genuardi, Maurizio; Neri, Giovanni; Chiurazzi, Pietro | |
1-gen-2020 | The emerging role of the BDNF-TrkB signaling pathway in the modulation of pain perception | Cappoli, N.; Tabolacci, E.; Aceto, P.; Dello Russo, C. | |
1-gen-2020 | Methylated premutation of the FMR1 gene in three sisters: correlating CGG expansion and epigenetic inactivation | Tabolacci, E.; Pomponi, M. G.; Remondini, L.; Pietrobono, R.; Nobile, V.; Pennacchio, G.; Gurrieri, F.; Neri, G.; Genuardi, M.; Chiurazzi, P. | |
1-gen-2019 | The mTOR kinase inhibitor rapamycin enhances the expression and release of pro-inflammatory cytokine interleukin 6 modulating the activation of human microglial cells. | Cappoli, N; Mezzogori, D; Tabolacci, E; Coletta, I; Navarra, P; Pani, G; Dello Russo, C. | |
1-gen-2017 | Simpson–Golabi–Behmel syndrome in a female: A case report and an unsolved issue | Vaisfeld, Alessandro; Pomponi, Maria Grazia; Pietrobono, Roberta; Tabolacci, Elisabetta; Neri, Giovanni | |
1-gen-2016 | CGG Repeat-Induced FMR1 Silencing Depends on the Expansion Size in Human iPSCs and Neurons Carrying Unmethylated Full Mutations | 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. | |
1-gen-2016 | Defining the role of the CGGBP1 protein in FMR1 gene expression | Goracci, Martina; Lanni, Stella; Mancano, Giorgia; Palumbo, Federica; Chiurazzi, Pietro; Neri, Giovanni; Tabolacci, Elisabetta | |
1-gen-2016 | Genome-wide methylation analysis demonstrates that 5-aza-2-deoxycytidine treatment does not cause random DNA demethylation in fragile X syndrome cells | Tabolacci, Elisabetta; Mancano, Giorgia; Lanni, Stella; Palumbo, Federica; Goracci, Martina; Ferrè, Fabrizio; Helmer Citterich, Manuela; Neri, Giovanni |