Browsing GGNB - Göttinger Graduiertenzentrum für Neurowissenschaften, Biophysik und molekulare Biowissenschaften by Advisor "Müller, Michael Prof. Dr."
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Redox imbalance and oxidative stress in Mecp2 deficient neurons
(2016-11-10)Rett syndrome is a neurodevelopmental disorder that primarily occurs in girls with a prevalence of 1:10.000–1:15.000 life births. The main genetic reasons of Rett syndrome are mutations in the methyl-CpG binding protein 2 ... -
Pharmacotreatment of a mouse model of Rett syndrome with the radical scavenger Trolox: Detailed assessment of potential merits in vitro and in vivo
(2015-04-27)Rett syndrome is a severe neurodevelopmental disorder, with an incidence of ~1/1000 female births, in which most patients carry mutations in the methyl-CpG binding protein 2 gene. No cure exists so far. Rett girls are born ...