D'Esposito M - Search Results

1

Blood-Brain Barrier Integrity Is Perturbed in a Mecp2-Null Mouse Model of Rett Syndrome.

Pepe G, Fioriniello S, Marracino F, Capocci L, Maglione V, D'Esposito M, Di Pardo A, Della Ragione F. Pepe G, et al. Biomolecules. 2023 Mar 28;13(4):606. doi: 10.3390/biom13040606. Biomolecules. 2023. PMID: 37189354 Free PMC article.

2

Oxidative brain damage in Mecp2-mutant murine models of Rett syndrome.

De Felice C, Della Ragione F, Signorini C, Leoncini S, Pecorelli A, Ciccoli L, Scalabrì F, Marracino F, Madonna M, Belmonte G, Ricceri L, De Filippis B, Laviola G, Valacchi G, Durand T, Galano JM, Oger C, Guy A, Bultel-Poncé V, Guy J, Filosa S, Hayek J, D'Esposito M. De Felice C, et al. Neurobiol Dis. 2014 Aug;68(100):66-77. doi: 10.1016/j.nbd.2014.04.006. Epub 2014 Apr 24. Neurobiol Dis. 2014. PMID: 24769161 Free PMC article.

3

Impairment of blood-brain barrier is an early event in R6/2 mouse model of Huntington Disease.

Di Pardo A, Amico E, Scalabrì F, Pepe G, Castaldo S, Elifani F, Capocci L, De Sanctis C, Comerci L, Pompeo F, D'Esposito M, Filosa S, Crispi S, Maglione V. Di Pardo A, et al. Sci Rep. 2017 Jan 24;7:41316. doi: 10.1038/srep41316. Sci Rep. 2017. PMID: 28117381 Free PMC article.

4

ATRX Contributes to MeCP2-Mediated Pericentric Heterochromatin Organization during Neural Differentiation.

Marano D, Fioriniello S, Fiorillo F, Gibbons RJ, D'Esposito M, Della Ragione F. Marano D, et al. Int J Mol Sci. 2019 Oct 29;20(21):5371. doi: 10.3390/ijms20215371. Int J Mol Sci. 2019. PMID: 31671722 Free PMC article.

5

MeCP2 and Major Satellite Forward RNA Cooperate for Pericentric Heterochromatin Organization.

Fioriniello S, Csukonyi E, Marano D, Brancaccio A, Madonna M, Zarrillo C, Romano A, Marracino F, Matarazzo MR, D'Esposito M, Della Ragione F. Fioriniello S, et al. Stem Cell Reports. 2020 Dec 8;15(6):1317-1332. doi: 10.1016/j.stemcr.2020.11.006. Stem Cell Reports. 2020. PMID: 33296675 Free PMC article.

6

Transcriptomic and Epigenomic Landscape in Rett Syndrome.

Marano D, Fioriniello S, D'Esposito M, Della Ragione F. Marano D, et al. Biomolecules. 2021 Jun 30;11(7):967. doi: 10.3390/biom11070967. Biomolecules. 2021. PMID: 34209228 Free PMC article. Review.

7

The X-linked methyl binding protein gene Kaiso is highly expressed in brain but is not mutated in Rett syndrome patients.

Della Ragione F, Tiunova A, Vacca M, Strazzullo M, González E, Armstrong J, Valero R, Campanile C, Pineda M, Hulten M, Monros E, D'Esposito M, Prokhortchouk E. Della Ragione F, et al. Gene. 2006 May 24;373:83-9. doi: 10.1016/j.gene.2006.01.015. Epub 2006 Mar 13. Gene. 2006. PMID: 16530985

8

Lessons from two human chromatin diseases, ICF syndrome and Rett syndrome.

Matarazzo MR, De Bonis ML, Vacca M, Della Ragione F, D'Esposito M. Matarazzo MR, et al. Int J Biochem Cell Biol. 2009 Jan;41(1):117-26. doi: 10.1016/j.biocel.2008.07.026. Epub 2008 Aug 22. Int J Biochem Cell Biol. 2009. PMID: 18786650 Review.

9

Effects of Mecp2 loss of function in embryonic cortical neurons: a bioinformatics strategy to sort out non-neuronal cells variability from transcriptome profiling.

Vacca M, Tripathi KP, Speranza L, Aiese Cigliano R, Scalabrì F, Marracino F, Madonna M, Sanseverino W, Perrone-Capano C, Guarracino MR, D'Esposito M. Vacca M, et al. BMC Bioinformatics. 2016 Jan 20;17 Suppl 2(Suppl 2):14. doi: 10.1186/s12859-015-0859-7. BMC Bioinformatics. 2016. PMID: 26821710 Free PMC article.

10

MECP2, a multi-talented modulator of chromatin architecture.

Della Ragione F, Vacca M, Fioriniello S, Pepe G, D'Esposito M. Della Ragione F, et al. Brief Funct Genomics. 2016 Nov;15(6):420-431. doi: 10.1093/bfgp/elw023. Epub 2016 Jun 12. Brief Funct Genomics. 2016. PMID: 27296483 Review.

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