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Cells|November 13, 2025
Polydatin Prevents UVA-Induced Damage in Human Dermal Fibroblasts by Maintaining Mitochondrial IntegrityBenedetta Niccolini, Alessia Riente, Duaa Hatem, et al.
Genes|May 4, 2026
NLRP12 as a Regulator of Inflammation: Insights into the Correlation with Autoinflammatory DisordersBeatrice Rosa, Elisabetta Tabolacci, Roberta Pietrobono, et al.
European Journal of Human Genetics : EJHG|September 26, 2024
New Insight into the genotype-phenotype correlation of PTH1R variants and primary failure of tooth eruption on an Italian CohortClarissa Modafferi, Elisabetta Tabolacci, Filomena Lo Vecchio, et al.
Plos One|February 12, 2009
Tumorigenic potential of olfactory bulb-derived human adult neural stem cells associates with activation of TERT and NOTCH1Patrizia Casalbore, Manuela Budoni, Lucia Ricci-Vitiani, et al.
Cells|March 11, 2023
Age-Dependent Dysregulation of APP in Neuronal and Skin Cells from Fragile X IndividualsGiulia Cencelli, Laura Pacini, Anastasia De Luca, et al.
European Journal of Medical Genetics|July 15, 2026
Two new cases of fragile X syndrome without CGG triplet expansion. Clinical-molecular characterization and review of the literatureGiulia Lauretti, Roberta Pietrobono, Benedetta Niccolini, et al.
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.
Genes|June 26, 2026
A Novel Variant of the CHD8 Gene in a Patient with Autism Spectrum DisorderElena Falcone, Alessia Bauleo, Laura De Stefano, 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.
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