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American Journal of Medical Genetics. Part A|October 15, 2013
Epigenetics, fragile X syndrome and transcriptional therapyElisabetta Tabolacci, Pietro ChiurazziMethods in Molecular Biology (Clifton, N.J.)|June 12, 2013
Epigenetic modifications of the FMR1 geneElisabetta Tabolacci, Giovanni NeriAmerican Journal of Medical Genetics. Part A|July 9, 2011
The FRAXopathies: definition, overview, and updateFilomena Pirozzi, Elisabetta Tabolacci, Giovanni NeriCritical Reviews in Clinical Laboratory Sciences|July 24, 2004
X-linked mental retardation (XLMR): from clinical conditions to cloned genesPietro Chiurazzi, Elisabetta Tabolacci, Giovanni NeriGenes|February 26, 2025
Syndromic and Non-Syndromic Primary Failure of Tooth Eruption: A Genetic OverviewClarissa Modafferi, Elisabetta Tabolacci, Cristina Grippaudo, et al.Genes|August 23, 2016
Transcriptional Reactivation of the FMR1 Gene. A Possible Approach to the Treatment of the Fragile X SyndromeElisabetta Tabolacci, Federica Palumbo, Veronica Nobile, et al.International Journal of Molecular Sciences|May 28, 2022
Mechanisms of the FMR1 Repeat Instability: How Does the CGG Sequence Expand?Elisabetta Tabolacci, Veronica Nobile, Cecilia Pucci, 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.Pageof 6