Genome-wide gene expression profiling of the Angelman syndrome mice with Ube3a mutation

Angelman syndrome (AS) is a human neurological disorder caused by lack of maternal UBE3A expression in the brain. Currently, the pathogenesis of AS, and how deficiency of maternal UBE3A can upset cellular homeostasis, remains vague. In this study, we performed a genomewide microarray analysis on the...

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Bibliographic Details
Main Authors: Low, Daren., Chen, Ken-Shiung.
Other Authors: School of Biological Sciences
Format: Article
Language:English
Published: 2011
Subjects:
Online Access:https://hdl.handle.net/10356/96280
http://hdl.handle.net/10220/7170
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Institution: Nanyang Technological University
Language: English
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