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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: guy j, guy a. 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.
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: guy j. Neurosci Res. 2016 Apr;105:28-34. doi: 10.1016/j.neures.2015.10.002. Epub 2015 Oct 20. Neurosci Res. 2016. PMID: 26476268
The role of MeCP2 in the brain.
Guy J, Cheval H, Selfridge J, Bird A. Guy J, et al. Annu Rev Cell Dev Biol. 2011;27:631-52. doi: 10.1146/annurev-cellbio-092910-154121. Epub 2011 Jun 29. Annu Rev Cell Dev Biol. 2011. PMID: 21721946 Review.
A mutation-led search for novel functional domains in MeCP2.
Guy J, Alexander-Howden B, FitzPatrick L, DeSousa D, Koerner MV, Selfridge J, Bird A. Guy J, et al. Hum Mol Genet. 2018 Jul 15;27(14):2531-2545. doi: 10.1093/hmg/ddy159. Hum Mol Genet. 2018. PMID: 29718204 Free PMC article.
Radically truncated MeCP2 rescues Rett syndrome-like neurological defects.
Tillotson R, Selfridge J, Koerner MV, Gadalla KKE, Guy J, De Sousa D, Hector RD, Cobb SR, Bird A. Tillotson R, et al. Among authors: guy j. Nature. 2017 Oct 19;550(7676):398-401. doi: 10.1038/nature24058. Epub 2017 Oct 11. Nature. 2017. PMID: 29019980 Free PMC article.
971 results