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Items: 1 to 20 of 23

1.

Inflammatory response in repeat breeder buffaloes.

Salzano A, Pesce A, D'Andrea L, Paciello O, Della Ragione F, Ciaramella P, Salzano C, Costagliola A, Licitra F, Neglia G.

Theriogenology. 2020 Jan 18;145:31-38. doi: 10.1016/j.theriogenology.2020.01.034. [Epub ahead of print]

PMID:
31982692
2.

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.

Int J Mol Sci. 2019 Oct 29;20(21). pii: E5371. doi: 10.3390/ijms20215371.

3.

Evaluation of factors involved in the failure of ovum capture in superovulated buffaloes.

Salzano A, De Canditiis C, Della Ragione F, Prandi A, Zullo G, Neglia G, Campanile G, Gasparrini B.

Theriogenology. 2018 Dec;122:102-108. doi: 10.1016/j.theriogenology.2018.09.007. Epub 2018 Sep 11.

PMID:
30245332
4.

Glycosphingolipid metabolic reprogramming drives neural differentiation.

Russo D, Della Ragione F, Rizzo R, Sugiyama E, Scalabrì F, Hori K, Capasso S, Sticco L, Fioriniello S, De Gregorio R, Granata I, Guarracino MR, Maglione V, Johannes L, Bellenchi GC, Hoshino M, Setou M, D'Esposito M, Luini A, D'Angelo G.

EMBO J. 2018 Apr 3;37(7). pii: e97674. doi: 10.15252/embj.201797674. Epub 2017 Dec 27.

5.

Reduced brain UCP2 expression mediated by microRNA-503 contributes to increased stroke susceptibility in the high-salt fed stroke-prone spontaneously hypertensive rat.

Rubattu S, Stanzione R, Bianchi F, Cotugno M, Forte M, Della Ragione F, Fioriniello S, D'Esposito M, Marchitti S, Madonna M, Baima S, Morelli G, Sciarretta S, Sironi L, Gelosa P, Volpe M.

Cell Death Dis. 2017 Jun 22;8(6):e2891. doi: 10.1038/cddis.2017.278.

6.

MECP2, a multi-talented modulator of chromatin architecture.

Della Ragione F, Vacca M, Fioriniello S, Pepe G, D'Esposito M.

Brief Funct Genomics. 2016 Nov;15(6):420-431. Epub 2016 Jun 12. Review.

PMID:
27296483
7.

X inactivation and reactivation in X-linked diseases.

Vacca M, Della Ragione F, Scalabrì F, D'Esposito M.

Semin Cell Dev Biol. 2016 Aug;56:78-87. doi: 10.1016/j.semcdb.2016.03.009. Epub 2016 Mar 17. Review.

PMID:
26994527
8.

Scavenger Receptor B1 oxidative post-translational modifications are responsible for its loss in Rett syndrome.

Valacchi G, Sticozzi C, Belmonte G, Cervellati F, Pecorelli A, Signorini C, Leoncini S, Ciccoli L, De Felice C, Della Ragione F, Scalabri F, Marracino F, Madonna M, D'Esposito M, Joussef H, Cervellati F, Stefania F.

Free Radic Biol Med. 2014 Oct;75 Suppl 1:S10-1. doi: 10.1016/j.freeradbiomed.2014.10.855. Epub 2014 Dec 10.

PMID:
26461280
9.

Experience-dependent DNA methylation regulates plasticity in the developing visual cortex.

Tognini P, Napoli D, Tola J, Silingardi D, Della Ragione F, D'Esposito M, Pizzorusso T.

Nat Neurosci. 2015 Jul;18(7):956-8. doi: 10.1038/nn.4026. Epub 2015 May 25.

PMID:
26005848
10.

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.

Neurobiol Dis. 2014 Aug;68:66-77. doi: 10.1016/j.nbd.2014.04.006. Epub 2014 Apr 24.

11.

Non-coding RNAs in chromatin disease involving neurological defects.

Della Ragione F, Gagliardi M, D'Esposito M, Matarazzo MR.

Front Cell Neurosci. 2014 Feb 25;8:54. doi: 10.3389/fncel.2014.00054. eCollection 2014. Review.

12.

Epigenetic control of hypoxia inducible factor-1α-dependent expression of placental growth factor in hypoxic conditions.

Tudisco L, Della Ragione F, Tarallo V, Apicella I, D'Esposito M, Matarazzo MR, De Falco S.

Epigenetics. 2014 Apr;9(4):600-10. doi: 10.4161/epi.27835. Epub 2014 Feb 6.

13.

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.

PLoS One. 2012;7(10):e47848. doi: 10.1371/journal.pone.0047848. Epub 2012 Oct 24.

14.

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

Della Ragione F, Filosa S, Scalabrì F, D'Esposito M.

Front Genet. 2012 Sep 11;3:181. doi: 10.3389/fgene.2012.00181. eCollection 2012.

15.

Absence of TI-VAMP/Vamp7 leads to increased anxiety in mice.

Danglot L, Zylbersztejn K, Petkovic M, Gauberti M, Meziane H, Combe R, Champy MF, Birling MC, Pavlovic G, Bizot JC, Trovero F, Della Ragione F, Proux-Gillardeaux V, Sorg T, Vivien D, D'Esposito M, Galli T.

J Neurosci. 2012 Feb 8;32(6):1962-8. doi: 10.1523/JNEUROSCI.4436-11.2012.

16.

Subclinical myocardial dysfunction in Rett syndrome.

De Felice C, Maffei S, Signorini C, Leoncini S, Lunghetti S, Valacchi G, D'Esposito M, Filosa S, Della Ragione F, Butera G, Favilli R, Ciccoli L, Hayek J.

Eur Heart J Cardiovasc Imaging. 2012 Apr;13(4):339-45. doi: 10.1093/ejechocard/jer256. Epub 2011 Nov 23.

PMID:
22113206
17.

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.

BMC Mol Biol. 2011 May 24;12:26. doi: 10.1186/1471-2199-12-26.

18.

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.

Clin Chim Acta. 2011 Jul 15;412(15-16):1399-406. doi: 10.1016/j.cca.2011.04.016. Epub 2011 Apr 17.

PMID:
21530498
19.

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.

J Mol Diagn. 2010 Nov;12(6):797-807. doi: 10.2353/jmoldx.2010.090199. Epub 2010 Sep 16.

20.

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.

Epigenetics. 2010 Jul 1;5(5):427-43. Epub 2010 Jul 1.

PMID:
20448464

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