Oxidative brain damage in Mecp2-mutant murine models of Rett syndrome-Reference-Cited by-同舟云学术

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Oxidative brain damage in Mecp2-mutant murine models of Rett syndrome

Published:2014-08 Issue: Volume:68 Page:66-77
ISSN:0969-9961
Container-title:Neurobiology of Disease
language:en
Short-container-title:Neurobiology of Disease

Author:

De Felice Claudio,Della Ragione Floriana,Signorini Cinzia,Leoncini Silvia,Pecorelli Alessandra,Ciccoli Lucia,Scalabrì Francesco,Marracino Federico,Madonna Michele,Belmonte Giuseppe,Ricceri Laura,De Filippis Bianca,Laviola Giovanni,Valacchi Giuseppe,Durand Thierry,Galano Jean-Marie,Oger Camille,Guy Alexandre,Bultel-Poncé Valérie,Guy Jacky,Filosa Stefania,Hayek Joussef,D'Esposito Maurizio

Funder

Bando Salute

AIR

UE Initial Training Network

MIUR-CNR

IRE-IFO

Publisher

Elsevier BV

Subject

Neurology

Reference76 articles.

1. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2;Amir;Nat. Genet.,1999

2. MeCP2 dependent heterochromatin reorganization during neural differentiation of a novel Mecp2-deficient embryonic stem cell reporter line;Bertulat;PLoS One,2012

3. Molecular genetics of Rett syndrome: when DNA methylation goes unrecognized;Bienvenu;Nat. Rev. Genet.,2006

4. A suppressor screen in Mecp2 mutant mice implicates cholesterol metabolism in Rett syndrome;Buchovecky;Nat. Genet.,2013

5. Nurse recognition of early deviation in development in home videos of infants with Rett disorder;Burford;J. Intellect. Disabil. Res.,2003

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