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Nucleic Acids Research|July 24, 2002
Quantitative analysis of DNA demethylation and transcriptional reactivation of the FMR1 gene in fragile X cells treated with 5-azadeoxycytidineRoberta Pietrobono, Maria Grazia Pomponi, Elisabetta Tabolacci, et al.
European Journal of Human Genetics : EJHG|March 3, 2005
Differential epigenetic modifications in the FMR1 gene of the fragile X syndrome after reactivating pharmacological treatmentsElisabetta Tabolacci, Roberta Pietrobono, Umberto Moscato, et al.
American Journal of Medical Genetics. Part A|February 14, 2006
A truncating mutation in the IL1RAPL1 gene is responsible for X-linked mental retardation in the MRX21 familyElisabetta Tabolacci, M Grazia Pomponi, Roberta Pietrobono, et al.
EXCLI Journal|May 23, 2023
Remifentanil does not affect human microglial immune activation in response to pro-inflammatory cytokinesCinzia Dello Russo, Natalia Cappoli, Elisabetta Tabolacci, et al.
Genes|February 25, 2023
RADX Gene Variant May Predispose to Familial Asperger SyndromeAlessia Azzarà, Roberto Rumore, Fulvia Brugnoletti, et al.
European Journal of Human Genetics : EJHG|August 27, 2015
Defining the role of the CGGBP1 protein in FMR1 gene expressionMartina Goracci, Stella Lanni, Giorgia Mancano, et al.
Antioxidants (Basel, Switzerland)|April 28, 2023
Rutin Protects Fibroblasts from UVA Radiation through Stimulation of Nrf2 PathwayElisabetta Tabolacci, Giuseppe Tringali, Veronica Nobile, et al.
EXCLI Journal|October 25, 2019
The mTOR kinase inhibitor rapamycin enhances the expression and release of pro-inflammatory cytokine interleukin 6 modulating the activation of human microglial cellsNatalia Cappoli, Daniele Mezzogori, Elisabetta Tabolacci, et al.
Pharmacogenetics and Genomics|July 16, 2008
Modest reactivation of the mutant FMR1 gene by valproic acid is accompanied by histone modifications but not DNA demethylationElisabetta Tabolacci, Ivana De Pascalis, Maria Accadia, et al.
Clinical Dysmorphology|June 3, 2005
Two brothers with 22q13 deletion syndrome and features suggestive of the Clark-Baraitser syndromeElisabetta Tabolacci, Marcella Zollino, Rosetta Lecce, et al.
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