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Page 1
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. Among authors: madonna m. 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.
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. Among authors: madonna m. 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.
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. Cortelazzo A, et al. Among authors: madonna m. Neurosci Res. 2016 Apr;105:28-34. doi: 10.1016/j.neures.2015.10.002. Epub 2015 Oct 20. Neurosci Res. 2016. PMID: 26476268
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. Rubattu S, et al. Among authors: madonna m. Cell Death Dis. 2017 Jun 22;8(6):e2891. doi: 10.1038/cddis.2017.278. Cell Death Dis. 2017. PMID: 28640254 Free PMC article.
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. Valacchi G, et al. Among authors: madonna m. Free Radic Biol Med. 2014 Oct;75 Suppl 1:S10-1. doi: 10.1016/j.freeradbiomed.2014.10.855. Epub 2014 Dec 10. Free Radic Biol Med. 2014. PMID: 26461280
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. Di Pardo A, et al. Among authors: madonna m. Sci Rep. 2018 May 24;8(1):8266. doi: 10.1038/s41598-018-23083-1. Sci Rep. 2018. PMID: 29795393 Free PMC article.
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. Di Pardo A, et al. Among authors: madonna m. Sci Rep. 2017 Jul 13;7(1):5280. doi: 10.1038/s41598-017-05709-y. Sci Rep. 2017. PMID: 28706199 Free PMC article.
The longevity-associated variant of BPIFB4 improves a CXCR4-mediated striatum-microglia crosstalk preventing disease progression in a mouse model of Huntington's disease.
Di Pardo A, Ciaglia E, Cattaneo M, Maciag A, Montella F, Lopardo V, Ferrario A, Villa F, Madonna M, Amico E, Carrizzo A, Damato A, Pepe G, Marracino F, Auricchio A, Vecchione C, Maglione V, Puca AA. Di Pardo A, et al. Among authors: madonna m. Cell Death Dis. 2020 Jul 18;11(7):546. doi: 10.1038/s41419-020-02754-w. Cell Death Dis. 2020. PMID: 32683420 Free PMC article.
Stimulation of S1PR5 with A-971432, a selective agonist, preserves blood-brain barrier integrity and exerts therapeutic effect in an animal model of Huntington's disease.
Di Pardo A, Castaldo S, Amico E, Pepe G, Marracino F, Capocci L, Giovannelli A, Madonna M, van Bergeijk J, Buttari F, van der Kam E, Maglione V. Di Pardo A, et al. Among authors: madonna m. Hum Mol Genet. 2018 Jul 15;27(14):2490-2501. doi: 10.1093/hmg/ddy153. Hum Mol Genet. 2018. PMID: 29688337
159 results