Systemic Radical Scavenger Treatment of a Mouse Model of Rett Syndrome: Merits and Limitations of the Vitamin E Derivative Trolox

Rett syndrome (RTT) is a severe neurodevelopmental disorder typically arising from spontaneous mutations in the X-chromosomal methyl-CpG binding protein 2 (MECP2) gene. The almost exclusively female Rett patients show an apparently normal development during their first 6–18 months of life. Subsequen...

Descrición completa

Gardado en:
Detalles Bibliográficos
Publicado en:Front Cell Neurosci
Main Authors: Janc, Oliwia A., Hüser, Marc A., Dietrich, Katharina, Kempkes, Belinda, Menzfeld, Christiane, Hülsmann, Swen, Müller, Michael
Formato: Artigo
Idioma:Inglês
Publicado: Frontiers Media S.A. 2016
Assuntos:
Neuroscience
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC5109403/
https://ncbi.nlm.nih.gov/pubmed/27895554
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fncel.2016.00266
Tags: Engadir etiqueta
Sen Etiquetas, Sexa o primeiro en etiquetar este rexistro!

Títulos similares