Elisabetta Tabolacci

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 21

Top Topics

Particulate Matter

Duchenne Muscular Dystrophy

Dna Methylation

Top Venues

International journal of molecular sciences

Antioxidants (Basel, Switzerland)

This page only lists publications with an associated author ORCID identifier.

Publications

Martina Grandi, Chiara Galber, Cristina Gatto, Veronica Nobile, Cecilia Pucci, Ida Schaldemose Nielsen, Francesco Boldrin, Giovanni Neri, Pietro Chiurazzi, Giancarlo Solaini, Alessandra Baracca, Valentina Giorgio, Elisabetta Tabolacci
Mitochondrial Dysfunction Causes Cell Death in Patients Affected by Fragile-X-Associated Disorders. International journal of molecular sciences 25 (6) (2024)
Martina Grandi, Chiara Galber, Cristina Gatto, Veronica Nobile, Cecilia Pucci, Ida Schaldemose Nielsen, Francesco Boldrin, Giovanni Neri, Pietro Chiurazzi, Giancarlo Solaini, Alessandra Baracca, Valentina Giorgio, Elisabetta Tabolacci
Mitochondrial Dysfunction Causes Cell Death in Patients Affected by Fragile-X-Associated Disorders. International journal of molecular sciences 25 (6) (2024)
Martina Grandi, Chiara Galber, Cristina Gatto, Veronica Nobile, Cecilia Pucci, Ida Schaldemose Nielsen, Francesco Boldrin, Giovanni Neri, Pietro Chiurazzi, Giancarlo Solaini, Alessandra Baracca, Valentina Giorgio, Elisabetta Tabolacci
Mitochondrial Dysfunction Causes Cell Death in Patients Affected by Fragile-X-Associated Disorders. International journal of molecular sciences 25 (6) (2024)
Giulia Cencelli, Laura Pacini, Anastasia De Luca, Ilenia Messia, Antonietta Gentile, Yunhee Kang, Veronica Nobile, Elisabetta Tabolacci, Peng Jin, Maria Giulia Farace, Claudia Bagni
Age-Dependent Dysregulation of APP in Neuronal and Skin Cells from Fragile X Individuals. Cells 12 (5) (2023)
Alessia Azzarà, Roberto Rumore, Fulvia Brugnoletti, Elisabetta Tabolacci, Irene Bottillo, Eugenio Sangiorgi, Fiorella Gurrieri
RADX Gene Variant May Predispose to Familial Asperger Syndrome. Genes 14 (2) (2023)
Giulia Cencelli, Laura Pacini, Anastasia De Luca, Ilenia Messia, Antonietta Gentile, Yunhee Kang, Veronica Nobile, Elisabetta Tabolacci, Peng Jin, Maria Giulia Farace, Claudia Bagni
Age-Dependent Dysregulation of APP in Neuronal and Skin Cells from Fragile X Individuals. Cells 12 (5) (2023)
Giulia Cencelli, Laura Pacini, Anastasia De Luca, Ilenia Messia, Antonietta Gentile, Yunhee Kang, Veronica Nobile, Elisabetta Tabolacci, Peng Jin, Maria Giulia Farace, Claudia Bagni
Age-Dependent Dysregulation of APP in Neuronal and Skin Cells from Fragile X Individuals. Cells 12 (5) (2023)
Elisabetta Tabolacci, Giuseppe Tringali, Veronica Nobile, Sara Duca, Michela Pizzoferrato, Patrizia Bottoni, Maria Elisabetta Clementi
Rutin Protects Fibroblasts from UVA Radiation through Stimulation of Nrf2 Pathway. Antioxidants (Basel, Switzerland) 12 (4) (2023)
Giulia Cencelli, Laura Pacini, Anastasia De Luca, Ilenia Messia, Antonietta Gentile, Yunhee Kang, Veronica Nobile, Elisabetta Tabolacci, Peng Jin, Maria Giulia Farace, Claudia Bagni
Age-Dependent Dysregulation of APP in Neuronal and Skin Cells from Fragile X Individuals. Cells 12 (5) (2023)
Alessia Azzarà, Roberto Rumore, Fulvia Brugnoletti, Elisabetta Tabolacci, Irene Bottillo, Eugenio Sangiorgi, Fiorella Gurrieri
RADX Gene Variant May Predispose to Familial Asperger Syndrome. Genes 14 (2) (2023)
Alessia Azzarà, Roberto Rumore, Fulvia Brugnoletti, Elisabetta Tabolacci, Irene Bottillo, Eugenio Sangiorgi, Fiorella Gurrieri
RADX Gene Variant May Predispose to Familial Asperger Syndrome. Genes 14 (2) (2023)
Alessia Azzarà, Roberto Rumore, Fulvia Brugnoletti, Elisabetta Tabolacci, Irene Bottillo, Eugenio Sangiorgi, Fiorella Gurrieri
RADX Gene Variant May Predispose to Familial Asperger Syndrome. Genes 14 (2) (2023)
Elisabetta Tabolacci, Giuseppe Tringali, Veronica Nobile, Sara Duca, Michela Pizzoferrato, Patrizia Bottoni, Maria Elisabetta Clementi
Rutin Protects Fibroblasts from UVA Radiation through Stimulation of Nrf2 Pathway. Antioxidants (Basel, Switzerland) 12 (4) (2023)
Filomena Lo Vecchio, Elisabetta Tabolacci, Veronica Nobile, Maria Grazia Pomponi, Roberta Pietrobono, Giovanni Neri, Simona Amenta, Ettore Candida, Cristina Grippaudo, Ettore Lo Cascio, Alessia Vita, Federica Tiberio, Alessandro Arcovito, Wanda Lattanzi, Maurizio Genuardi, Pietro Chiurazzi
Mother and Daughter Carrying of the Same Pathogenic Variant in FGFR2 with Discordant Phenotype. Genes 13 (7) (2022)
Elisabetta Tabolacci, Veronica Nobile, Cecilia Pucci, Pietro Chiurazzi
Mechanisms of the FMR1 Repeat Instability: How Does the CGG Sequence Expand? International journal of molecular sciences 23 (10) (2022)
Elisabetta Tabolacci, Maria Grazia Pomponi, Laura Remondini, Roberta Pietrobono, Daniela Orteschi, Veronica Nobile, Cecilia Pucci, Elisa Musto, Marika Pane, Eugenio M Mercuri, Giovanni Neri, Maurizio Genuardi, Pietro Chiurazzi, Marcella Zollino
Co-Occurrence of Fragile X Syndrome with a Second Genetic Condition: Three Independent Cases of Double Diagnosis. Genes 12 (12) (2021)
Veronica Nobile, Cecilia Pucci, Pietro Chiurazzi, Giovanni Neri, Elisabetta Tabolacci
DNA Methylation, Mechanisms of FMR1 Inactivation and Therapeutic Perspectives for Fragile X Syndrome. Biomolecules 11 (2) (2021)
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 Maria Tabano, Elisabetta Tabolacci, Isabella Torrente, Maurizio Genuardi, Giovanni Neri, Andrea Riccio
DNA Methylation in the Diagnosis of Monogenic Diseases. Genes 11 (4) (2020)
Elisabetta Tabolacci, Clelia Molinario, Giuseppe Marangi, Veronica Nobile, Vincenzo Arena, Marisa I Mendes, Desiree E C Smith, Gajja S Salomons, Milena Tana, Simonetta Costa, Giovanni Vento, Maurizio Genuardi
Infantile Liver Failure Syndrome 1 associated with a novel variant of the LARS1 gene: Clinical, genetic, and functional characterization. Clinical genetics 99 (4) (2020)
Veronica Nobile, Federica Palumbo, Stella Lanni, Valentina Ghisio, Alberto Vitali, Massimo Castagnola, Valeria Marzano, Giuseppe Maulucci, Claudio De Angelis, Marco De Spirito, Laura Pacini, Laura D'Andrea, Rino Ragno, Giulia Stazi, Sergio Valente, Antonello Mai, Pietro Chiurazzi, Maurizio Genuardi, Giovanni Neri, Elisabetta Tabolacci
Altered mitochondrial function in cells carrying a premutation or unmethylated full mutation of the FMR1 gene. Human genetics 139 (2) (2020)
Elisabetta Tabolacci, Maria Grazia Pomponi, Laura Remondini, Roberta Pietrobono, Veronica Nobile, Gaetana Pennacchio, Fiorella Gurrieri, Giovanni Neri, Maurizio Genuardi, Pietro Chiurazzi
Methylated premutation of the FMR1 gene in three sisters: correlating CGG expansion and epigenetic inactivation. European journal of human genetics : EJHG 28 (5) (2019)