Della Ragione F - Search Results

1

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. Among authors: della ragione f. Liver Transpl. 2007 Jan;13(1):99-113. doi: 10.1002/lt.20960. Liver Transpl. 2007. PMID: 17192907 Free article.

2

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

3

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

4

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. Among authors: della ragione f. 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.

5

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. Among authors: della ragione f. Epigenetics. 2010 Jul 1;5(5):427-43. doi: 10.4161/epi.5.5.11999. Epub 2010 Jul 1. Epigenetics. 2010. PMID: 20448464 Free article.

6

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.

7

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. Among authors: della ragione f. BMC Mol Biol. 2011 May 24;12:26. doi: 10.1186/1471-2199-12-26. BMC Mol Biol. 2011. PMID: 21609427 Free PMC article.

8

MeCP2 as a genome-wide modulator: the renewal of an old story.

Della Ragione F, Filosa S, Scalabrì F, D'Esposito M. Della Ragione F, et al. Front Genet. 2012 Sep 11;3:181. doi: 10.3389/fgene.2012.00181. eCollection 2012. Front Genet. 2012. PMID: 22973303 Free PMC article.

9

MeCP2 dependent heterochromatin reorganization during neural differentiation of a novel Mecp2-deficient embryonic stem cell reporter line.

Bertulat B, De Bonis ML, Della Ragione F, Lehmkuhl A, Milden M, Storm C, Jost KL, Scala S, Hendrich B, D'Esposito M, Cardoso MC. Bertulat B, et al. Among authors: della ragione f. PLoS One. 2012;7(10):e47848. doi: 10.1371/journal.pone.0047848. Epub 2012 Oct 24. PLoS One. 2012. PMID: 23112857 Free PMC article.

10

Non-coding RNAs in chromatin disease involving neurological defects.

Della Ragione F, Gagliardi M, D'Esposito M, Matarazzo MR. Della Ragione F, et al. Front Cell Neurosci. 2014 Feb 25;8:54. doi: 10.3389/fncel.2014.00054. eCollection 2014. Front Cell Neurosci. 2014. PMID: 24616662 Free PMC article. Review.

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