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Page 1
Mechanisms of the FMR1 Repeat Instability: How Does the CGG Sequence Expand?
Int J Mol Sci. 2022 May 12;23(10):5425. doi: 10.3390/ijms23105425.
Int J Mol Sci. 2022.
PMID: 35628235
Free PMC article.
Review.
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: pucci c.
Biomolecules. 2021 Feb 16;11(2):296. doi: 10.3390/biom11020296.
Biomolecules. 2021.
PMID: 33669384
Free PMC article.
Review.
Item in Clipboard
CRISPR/Cas9-Induced Inactivation of the Autism-Risk Gene setd5 Leads to Social Impairments in Zebrafish.
Gabellini C, Pucci C, De Cesari C, Martini D, Di Lauro C, Digregorio M, Norton W, Zippo A, Sessa A, Broccoli V, Andreazzoli M.
Gabellini C, et al. Among authors: pucci c.
Int J Mol Sci. 2022 Dec 22;24(1):167. doi: 10.3390/ijms24010167.
Int J Mol Sci. 2022.
PMID: 36613611
Free PMC article.
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Mitochondrial Dysfunction Causes Cell Death in Patients Affected by Fragile-X-Associated Disorders.
Grandi M, Galber C, Gatto C, Nobile V, Pucci C, Schaldemose Nielsen I, Boldrin F, Neri G, Chiurazzi P, Solaini G, Baracca A, Giorgio V, Tabolacci E.
Grandi M, et al. Among authors: pucci c.
Int J Mol Sci. 2024 Mar 18;25(6):3421. doi: 10.3390/ijms25063421.
Int J Mol Sci. 2024.
PMID: 38542395
Free PMC article.
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SETD5 Regulates Chromatin Methylation State and Preserves Global Transcriptional Fidelity during Brain Development and Neuronal Wiring.
Sessa A, Fagnocchi L, Mastrototaro G, Massimino L, Zaghi M, Indrigo M, Cattaneo S, Martini D, Gabellini C, Pucci C, Fasciani A, Belli R, Taverna S, Andreazzoli M, Zippo A, Broccoli V.
Sessa A, et al. Among authors: pucci c.
Neuron. 2019 Oct 23;104(2):271-289.e13. doi: 10.1016/j.neuron.2019.07.013. Epub 2019 Sep 9.
Neuron. 2019.
PMID: 31515109
Free article.
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Exposure to the natural alkaloid Berberine affects cardiovascular system morphogenesis and functionality during zebrafish development.
Martini D, Pucci C, Gabellini C, Pellegrino M, Andreazzoli M.
Martini D, et al. Among authors: pucci c.
Sci Rep. 2020 Oct 15;10(1):17358. doi: 10.1038/s41598-020-73661-5.
Sci Rep. 2020.
PMID: 33060638
Free PMC article.
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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: pucci c.
Genes (Basel). 2021 Nov 27;12(12):1909. doi: 10.3390/genes12121909.
Genes (Basel). 2021.
PMID: 34946857
Free PMC article.
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