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Items: 1 to 20 of 51

1.

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.

2.

Author Correction: Defective Sphingosine-1-phosphate metabolism is a druggable target in Huntington's disease.

Di Pardo A, Amico E, Basit A, Armirotti A, Joshi P, Neely MD, Vuono R, Castaldo S, Digilio AF, Scalabrì F, Pepe G, Elifani F, Madonna M, Jeong SK, Park BM, D'Esposito M, Bowman AB, Barker RA, Maglione V.

Sci Rep. 2018 May 24;8(1):8266. doi: 10.1038/s41598-018-23083-1.

3.

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.

4.

Retention of Mitochondria in Mature Human Red Blood Cells as the Result of Autophagy Impairment in Rett Syndrome.

Sbardella D, Tundo GR, Campagnolo L, Valacchi G, Orlandi A, Curatolo P, Borsellino G, D'Esposito M, Ciaccio C, Cesare SD, Pierro DD, Galasso C, Santarone ME, Hayek J, Coletta M, Marini S.

Sci Rep. 2017 Sep 26;7(1):12297. doi: 10.1038/s41598-017-12069-0.

5.

Defective Sphingosine-1-phosphate metabolism is a druggable target in Huntington's disease.

Di Pardo A, Amico E, Basit A, Armirotti A, Joshi P, Neely MD, Vuono R, Castaldo S, Digilio AF, Scalabrì F, Pepe G, Elifani F, Madonna M, Jeong SK, Park BM, D'Esposito M, Bowman AB, Barker RA, Maglione V.

Sci Rep. 2017 Jul 13;7(1):5280. doi: 10.1038/s41598-017-05709-y. Erratum in: Sci Rep. 2018 May 24;8(1):8266.

6.

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.

7.

ICF-specific DNMT3B dysfunction interferes with intragenic regulation of mRNA transcription and alternative splicing.

Gatto S, Gagliardi M, Franzese M, Leppert S, Papa M, Cammisa M, Grillo G, Velasco G, Francastel C, Toubiana S, D'Esposito M, Angelini C, Matarazzo MR.

Nucleic Acids Res. 2017 Jun 2;45(10):5739-5756. doi: 10.1093/nar/gkx163.

8.

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.

Sci Rep. 2017 Jan 24;7:41316. doi: 10.1038/srep41316.

9.

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
10.

Anti-Mullerian hormone (AMH) concentration in follicular fluid and mRNA expression of AMH receptor type II and LH receptor in granulosa cells as predictive markers of good buffalo (Bubalus bubalis) donors.

Liang A, Salzano A, D'Esposito M, Comin A, Montillo M, Yang L, Campanile G, Gasparrini B.

Theriogenology. 2016 Sep 1;86(4):963-970. doi: 10.1016/j.theriogenology.2016.03.020. Epub 2016 Mar 19.

PMID:
27087535
11.

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
12.

MECP2 Duplication Syndrome: Evidence of Enhanced Oxidative Stress. A Comparison with Rett Syndrome.

Signorini C, De Felice C, Leoncini S, Møller RS, Zollo G, Buoni S, Cortelazzo A, Guerranti R, Durand T, Ciccoli L, D'Esposito M, Ravn K, Hayek J.

PLoS One. 2016 Mar 1;11(3):e0150101. doi: 10.1371/journal.pone.0150101. eCollection 2016.

13.

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.

BMC Bioinformatics. 2016 Jan 20;17 Suppl 2:14. doi: 10.1186/s12859-015-0859-7.

14.

Abnormal N-glycosylation pattern for brain nucleotide pyrophosphatase-5 (NPP-5) in Mecp2-mutant murine models of Rett syndrome.

Cortelazzo A, De Felice C, Guerranti R, Signorini C, Leoncini S, Pecorelli A, Scalabrì F, Madonna M, Filosa S, Della Giovampaola C, Capone A, Durand T, Mirasole C, Zolla L, Valacchi G, Ciccoli L, Guy J, D'Esposito M, Hayek J.

Neurosci Res. 2016 Apr;105:28-34. doi: 10.1016/j.neures.2015.10.002. Epub 2015 Oct 20.

PMID:
26476268
15.

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
16.

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
17.

Exploring the possible link between MeCP2 and oxidative stress in Rett syndrome.

Filosa S, Pecorelli A, D'Esposito M, Valacchi G, Hajek J.

Free Radic Biol Med. 2015 Nov;88(Pt A):81-90. doi: 10.1016/j.freeradbiomed.2015.04.019. Epub 2015 May 8. Review.

PMID:
25960047
18.

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.

19.

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.

20.

Global transcriptome profiles of Italian Mediterranean buffalo embryos with normal and retarded growth.

Strazzullo M, Gasparrini B, Neglia G, Balestrieri ML, Francioso R, Rossetti C, Nassa G, De Filippo MR, Weisz A, Di Francesco S, Vecchio D, D'Esposito M, D'Occhio MJ, Zicarelli L, Campanile G.

PLoS One. 2014 Feb 28;9(2):e90027. doi: 10.1371/journal.pone.0090027. eCollection 2014.

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