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Epigenetics & Chromatin|March 26, 2016
Genome-wide methylation analysis demonstrates that 5-aza-2-deoxycytidine treatment does not cause random DNA demethylation in fragile X syndrome cellsElisabetta Tabolacci, Giorgia Mancano, Stella Lanni, et al.Pain|December 4, 2023
Remifentanil-induced hyperalgesia in healthy volunteers: a systematic review and meta-analysis of randomized controlled trialsCinzia Dello Russo, Valeria Di Franco, Elisabetta Tabolacci, et al.Human Molecular Genetics|November 26, 2004
Molecular dissection of the events leading to inactivation of the FMR1 geneRoberta Pietrobono, Elisabetta Tabolacci, Francesca Zalfa, et al.European Journal of Human Genetics : EJHG|December 6, 2019
Methylated premutation of the FMR1 gene in three sisters: correlating CGG expansion and epigenetic inactivationElisabetta Tabolacci, Maria Grazia Pomponi, Laura Remondini, et al.Plos Genetics|July 23, 2013
Role of CTCF protein in regulating FMR1 locus transcriptionStella Lanni, Martina Goracci, Loredana Borrelli, et al.Journal of Photochemistry and Photobiology. B, Biology|March 27, 2026
Subcellular photoprotection through precision nutraceuticals: Divergent actions of rutin and punicalagin on redox and mitochondrial homeostasis in human dermal fibroblastsAlessia Riente, Flavio Di Giacinto, Michele Maria De Giulio, et al.Human Mutation|July 29, 2011
Insertion of 16 amino acids in the BAR domain of the oligophrenin 1 protein causes mental retardation and cerebellar hypoplasia in an Italian familyFilomena Pirozzi, Francesca Romana Di Raimo, Ginevra Zanni, et al.Movement Disorders : Official Journal of the Movement Disorder Society|December 7, 2006
Prevalence of spinocerebellar ataxia type 2 mutation among Italian Parkinsonian patientsAnna Modoni, Maria Fiorella Contarino, Anna Rita Bentivoglio, et al.Genes|March 1, 2020
Reversion to Normal of FMR1 Expanded Alleles: A Rare Event in Two Independent Fragile X Syndrome FamiliesElisabetta Tabolacci, Roberta Pietrobono, Giulia Maneri, et al.American Journal of Medical Genetics. Part A|May 27, 2010
Treatment with valproic acid ameliorates ADHD symptoms in fragile X syndrome boysMariagiulia Torrioli, Silvia Vernacotola, Chiara Setini, et al.Pageof 6