Physiological properties of cerebellar circuits in a mouse model for Angelman Syndrome and modulation of inhibitory transmission by NMDA receptor activation in the mouse hippocampus

UBE3A encodes the ubiquitin ligase E6-AP and the point mutation of this gene causes severe neurological disorder called Angelman Syndrome (AS) in a young child. To elucidate the molecular basis of AS pathogenesis and promote the design of rational therapies for AS patient, an Ube3a null mutation mou...

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書目詳細資料
主要作者: Xue, Jiu Gang
其他作者: Law Sai-Kit, Alex
格式: Theses and Dissertations
語言:English
出版: 2013
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在線閱讀:https://hdl.handle.net/10356/51022
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