Federica Palumbo - Search Results

Year	Number of Results
2013	1
2014	1
2015	1
2016	3
2020	1
2021	1
2024	0

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: palumbo f. Genes (Basel). 2016 Aug 17;7(8):49. doi: 10.3390/genes7080049. Genes (Basel). 2016. PMID: 27548224 Free PMC article. Review.

2

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: palumbo f. 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.

3

Performance of conventional cytogenetic analysis on chorionic villi when only one cell layer, cytotrophoblast or mesenchyme alone, is analyzed.

Grati FR, Malvestiti F, Gallazzi G, Saragozza S, Grimi B, Agrati C, Branca L, Palumbo F, Trotta A, Chinetti S, Simoni G, Ferreira J, Benn P. Grati FR, et al. Among authors: palumbo f. Prenat Diagn. 2021 May;41(6):652-660. doi: 10.1002/pd.5941. Epub 2021 Apr 10. Prenat Diagn. 2021. PMID: 33782989

4

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: palumbo f. Hum Genet. 2020 Feb;139(2):227-245. doi: 10.1007/s00439-019-02104-7. Epub 2020 Jan 9. Hum Genet. 2020. PMID: 31919630

5

Need and disparities in primary care management of patients with diabetes.

Buja A, Gini R, Visca M, Damiani G, Federico B, Donato D, Francesconi P, Marini A, Donatini A, Brugaletta S, Bardelle G, Baldo V, Bellentani M; Valore Project. Buja A, et al. BMC Endocr Disord. 2014 Jul 10;14:56. doi: 10.1186/1472-6823-14-56. BMC Endocr Disord. 2014. PMID: 25011729 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: palumbo f. 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

Prevalence of chronic diseases by immigrant status and disparities in chronic disease management in immigrants: a population-based cohort study, Valore Project.

Buja A, Gini R, Visca M, Damiani G, Federico B, Francesconi P, Donato D, Marini A, Donatini A, Brugaletta S, Baldo V, Bellentani M; Valore Project. Buja A, et al. BMC Public Health. 2013 May 24;13:504. doi: 10.1186/1471-2458-13-504. BMC Public Health. 2013. PMID: 23706129 Free PMC article.

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