Neri G - Search Results

1

Transcriptional Reactivation of the FMR1 Gene. A Possible Approach to the Treatment of the Fragile X Syndrome.

Tabolacci E, Palumbo F, Nobile V, Neri G. Tabolacci E, et al. Among authors: neri g. Genes (Basel). 2016 Aug 17;7(8):49. doi: 10.3390/genes7080049. Genes (Basel). 2016. PMID: 27548224 Free PMC article. Review.

2

Modest reactivation of the mutant FMR1 gene by valproic acid is accompanied by histone modifications but not DNA demethylation.

Tabolacci E, De Pascalis I, Accadia M, Terracciano A, Moscato U, Chiurazzi P, Neri G. Tabolacci E, et al. Among authors: neri g. Pharmacogenet Genomics. 2008 Aug;18(8):738-41. doi: 10.1097/FPC.0b013e32830500a1. Pharmacogenet Genomics. 2008. PMID: 18622267

3

Epigenetic analysis reveals a euchromatic configuration in the FMR1 unmethylated full mutations.

Tabolacci E, Moscato U, Zalfa F, Bagni C, Chiurazzi P, Neri G. Tabolacci E, et al. Among authors: neri g. Eur J Hum Genet. 2008 Dec;16(12):1487-98. doi: 10.1038/ejhg.2008.130. Epub 2008 Jul 16. Eur J Hum Genet. 2008. PMID: 18628788

4

Epigenetic modifications of the FMR1 gene.

Tabolacci E, Neri G. Tabolacci E, et al. Among authors: neri g. Methods Mol Biol. 2013;1010:141-53. doi: 10.1007/978-1-62703-411-1_10. Methods Mol Biol. 2013. PMID: 23754224

5

Defining the role of the CGGBP1 protein in FMR1 gene expression.

Goracci M, Lanni S, Mancano G, Palumbo F, Chiurazzi P, Neri G, Tabolacci E. Goracci M, et al. Among authors: neri g. Eur J Hum Genet. 2016 May;24(5):697-703. doi: 10.1038/ejhg.2015.182. Epub 2015 Aug 26. Eur J Hum Genet. 2016. PMID: 26306647 Free PMC article.

6

Genome-wide methylation analysis demonstrates that 5-aza-2-deoxycytidine treatment does not cause random DNA demethylation in fragile X syndrome cells.

Tabolacci E, Mancano G, Lanni S, Palumbo F, Goracci M, Ferrè F, Helmer-Citterich M, Neri G. Tabolacci E, et al. Among authors: neri g. Epigenetics Chromatin. 2016 Mar 24;9:12. doi: 10.1186/s13072-016-0060-x. eCollection 2016. Epigenetics Chromatin. 2016. PMID: 27014370 Free PMC article.

7

DNA Methylation, Mechanisms of FMR1 Inactivation and Therapeutic Perspectives for Fragile X Syndrome.

Nobile V, Pucci C, Chiurazzi P, Neri G, Tabolacci E. Nobile V, et al. Among authors: neri g. Biomolecules. 2021 Feb 16;11(2):296. doi: 10.3390/biom11020296. Biomolecules. 2021. PMID: 33669384 Free PMC article. Review.

8

Altered mitochondrial function in cells carrying a premutation or unmethylated full mutation of the FMR1 gene.

Nobile V, Palumbo F, Lanni S, Ghisio V, Vitali A, Castagnola M, Marzano V, Maulucci G, De Angelis C, De Spirito M, Pacini L, D'Andrea L, Ragno R, Stazi G, Valente S, Mai A, Chiurazzi P, Genuardi M, Neri G, Tabolacci E. Nobile V, et al. Among authors: neri g. Hum Genet. 2020 Feb;139(2):227-245. doi: 10.1007/s00439-019-02104-7. Epub 2020 Jan 9. Hum Genet. 2020. PMID: 31919630

9

Reversion to Normal of FMR1 Expanded Alleles: A Rare Event in Two Independent Fragile X Syndrome Families.

Tabolacci E, Pietrobono R, Maneri G, Remondini L, Nobile V, Della Monica M, Pomponi MG, Genuardi M, Neri G, Chiurazzi P. Tabolacci E, et al. Among authors: neri g. Genes (Basel). 2020 Feb 26;11(3):248. doi: 10.3390/genes11030248. Genes (Basel). 2020. PMID: 32111011 Free PMC article.

10

Co-Occurrence of Fragile X Syndrome with a Second Genetic Condition: Three Independent Cases of Double Diagnosis.

Tabolacci E, Pomponi MG, Remondini L, Pietrobono R, Orteschi D, Nobile V, Pucci C, Musto E, Pane M, Mercuri EM, Neri G, Genuardi M, Chiurazzi P, Zollino M. Tabolacci E, et al. Among authors: neri g. Genes (Basel). 2021 Nov 27;12(12):1909. doi: 10.3390/genes12121909. Genes (Basel). 2021. PMID: 34946857 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

908 results

Search Page