D'Esposito M - Search Results

1

Epigenetic Factors That Control Pericentric Heterochromatin Organization in Mammals.

Fioriniello S, Marano D, Fiorillo F, D'Esposito M, Della Ragione F. Fioriniello S, et al. Genes (Basel). 2020 May 28;11(6):595. doi: 10.3390/genes11060595. Genes (Basel). 2020. PMID: 32481609 Free PMC article. Review.

2

MECP2 gene mutation analysis in the British and Italian Rett Syndrome patients: hot spot map of the most recurrent mutations and bioinformatic analysis of a new MECP2 conserved region.

Vacca M, Filippini F, Budillon A, Rossi V, Della Ragione F, De Bonis ML, Mercadante G, Manzati E, Gualandi F, Bigoni S, Trabanelli C, Pini G, Calzolari E, Ferlini A, Meloni I, Hayek G, Zappella M, Renieri A, D'Urso M, D'Esposito M, Macdonald F, Kerr A, Dhanjal S, Hulten M. Vacca M, et al. Brain Dev. 2001 Dec;23 Suppl 1:S246-50. doi: 10.1016/s0387-7604(01)00343-6. Brain Dev. 2001. PMID: 11738884

3

Molecular cloning and characterization of the clock gene period2 in the testis of lizard Podarcis sicula and its expression during seasonal reproductive cycle.

Della Ragione F, Comitato R, Angelini F, D'Esposito M, Cardone A. Della Ragione F, et al. Gene. 2005 Dec 19;363:105-12. doi: 10.1016/j.gene.2005.08.018. Epub 2005 Nov 14. Gene. 2005. PMID: 16289937

4

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

5

Wide gene expression profiling of ischemia-reperfusion injury in human liver transplantation.

Conti A, Scala S, D'Agostino P, Alimenti E, Morelli D, Andria B, Tammaro A, Attanasio C, Della Ragione F, Scuderi V, Fabbrini F, D'Esposito M, Di Florio E, Nitsch L, Calise F, Faiella A. Conti A, et al. Liver Transpl. 2007 Jan;13(1):99-113. doi: 10.1002/lt.20960. Liver Transpl. 2007. PMID: 17192907 Free article.

6

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.

7

Epigenetic alteration of microRNAs in DNMT3B-mutated patients of ICF syndrome.

Gatto S, Della Ragione F, Cimmino A, Strazzullo M, Fabbri M, Mutarelli M, Ferraro L, Weisz A, D'Esposito M, Matarazzo MR. Gatto S, et al. Epigenetics. 2010 Jul 1;5(5):427-43. doi: 10.4161/epi.5.5.11999. Epub 2010 Jul 1. Epigenetics. 2010. PMID: 20448464

8

Differential DNA methylation as a tool for noninvasive prenatal diagnosis (NIPD) of X chromosome aneuploidies.

Della Ragione F, Mastrovito P, Campanile C, Conti A, Papageorgiou EA, Hultén MA, Patsalis PC, Carter NP, D'Esposito M. Della Ragione F, et al. J Mol Diagn. 2010 Nov;12(6):797-807. doi: 10.2353/jmoldx.2010.090199. Epub 2010 Sep 16. J Mol Diagn. 2010. PMID: 20847278 Free PMC article.

9

F₄-neuroprostanes mediate neurological severity in Rett syndrome.

Signorini C, De Felice C, Leoncini S, Giardini A, D'Esposito M, Filosa S, Della Ragione F, Rossi M, Pecorelli A, Valacchi G, Ciccoli L, Hayek J. Signorini C, et al. Clin Chim Acta. 2011 Jul 15;412(15-16):1399-406. doi: 10.1016/j.cca.2011.04.016. Epub 2011 Apr 17. Clin Chim Acta. 2011. PMID: 21530498

10

Alternative splicing of the human gene SYBL1 modulates protein domain architecture of Longin VAMP7/TI-VAMP, showing both non-SNARE and synaptobrevin-like isoforms.

Vacca M, Albania L, Della Ragione F, Carpi A, Rossi V, Strazzullo M, De Franceschi N, Rossetto O, Filippini F, D'Esposito M. Vacca M, et al. BMC Mol Biol. 2011 May 24;12:26. doi: 10.1186/1471-2199-12-26. BMC Mol Biol. 2011. PMID: 21609427 Free PMC article.

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