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Nature Neuroscience|April 10, 2007
A new function for the fragile X mental retardation protein in regulation of PSD-95 mRNA stabilityFrancesca Zalfa, Boris Eleuteri, Kirsten S Dickson, et al.International Journal of Molecular Sciences|March 28, 2024
Mitochondrial Dysfunction Causes Cell Death in Patients Affected by Fragile-X-Associated DisordersMartina Grandi, Chiara Galber, Cristina Gatto, et al.Journal of Neuroimmunology|October 1, 2020
The emerging role of the BDNF-TrkB signaling pathway in the modulation of pain perceptionNatalia Cappoli, Elisabetta Tabolacci, Paola Aceto, et al.Genes|March 28, 2026
Genetic Determinants of Primary Failure of Eruption: A Comprehensive Review of PTH1R VariantsBenedetta Niccolini, Giulia Lauretti, Pietro Chiurazzi, et al.Journal of Neurodevelopmental Disorders|April 26, 2025
Transcriptomic profiling of unmethylated full mutation carriers implicates TET3 in FMR1 CGG repeat expansion methylation dynamics in fragile X syndromeGrace Farmiloe, Veronika Bejczy, Elisabetta Tabolacci, et al.Genes|December 24, 2021
Co-Occurrence of Fragile X Syndrome with a Second Genetic Condition: Three Independent Cases of Double DiagnosisElisabetta Tabolacci, Maria Grazia Pomponi, Laura Remondini, et al.Human Mutation|January 16, 2007
MID1 mutation screening in a large cohort of Opitz G/BBB syndrome patients: twenty-nine novel mutations identifiedRosa Ferrentino, Maria Teresa Bassi, David Chitayat, et al.Progress in Orthodontics|July 3, 2025
Permanent first molar eruption failure in children: leading signs for early diagnosisCristina Grippaudo, Elisabetta Tabolacci, Marco Farronato, et al.European Journal of Pharmacology|May 3, 2025
The role of sevoflurane exposure on systemic inflammation and neuroinflammation: a systematic review and meta-analysis of in vivo and in vitro studiesFrancesca Rapido, Valeria Di Franco, Elisabetta Tabolacci, et al.Pageof 30