Alterations of cortical and hippocampal EEG activity in MeCP2-deficient mice

Alterations of cortical and hippocampal EEG activity in MeCP2-deficient mice

Rett syndrome is a pediatric neurological condition caused by mutations of the gene encoding the transcriptional regulator MECP2. In this study, we examined cortical and hippocampal electroencephalographic (EEG) activity in male and female MeCP2-deficient mice at symptomatic stages during different...

Full description

Bibliographic Details
Main Authors: Jennifer Anne D'Cruz, Chiping Wu, Tariq Zahid, Youssef El-Hayek, Liang Zhang, James H. Eubanks
Format: Article
Language:English
Published: Elsevier 2010-04-01
Series:Neurobiology of Disease
Subjects:
Rett syndrome
Electroencephalography
Mutant mice
Autism-spectrum disorder
Methyl DNA-binding factor
Network synchrony
Online Access:http://www.sciencedirect.com/science/article/pii/S0969996109003738

Internet

http://www.sciencedirect.com/science/article/pii/S0969996109003738

Similar Items