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Now showing items 1-6 of 6

Date	Title	Author	Type
2010	Genetic studies of Prader-Willi patients from Taiwan identify two patients with atypical deletions and provide evidences for conservation of genomic architecture in proximal chromosome 15q.	Hou, Aihua.; Lin, Shuan Pei.; Ho, Shi Yun.; Chen, Jennifer Chi Fung.; Lin, Hsiang Yu.; Chen, Yen Jiun.; Huang, Chi Yu.; Chiu, Hui Ching.; Chuang, Chih Kuang.; Chen, Ken Shiung.	Journal Article
2010	Genome-wide gene expression profiling of the Angelman syndrome mice with Ube3a mutation.	Low, Daren.; Chen, Ken Shiung.	Journal Article
2011	NMDA receptor activation enhances inhibitory GABAergic transmission onto hippocampal pyramidal neurons via presynaptic and postsynaptic mechanisms.	Xue, Jiu Gang.; Masuoka, Takayoshi.; Gong, Xian Di.; Chen, Ken Shiung.; Yanagawa, Yuchio.; Law, Alex Sai Kit.; Konishi, Shiro.	Journal Article
2011	Rasd1 interacts with Ear2 (Nr2f6) to regulate renin transcription.	Tan, Jen Jen.; Ong, Angeline Shufen.; Chen, Ken Shiung.	Journal Article
2011	Rasd1 modulates the coactivator function of NonO in the cyclic AMP pathway.	Ong, Angeline Shufen.; Tan, Jen Jen.; Tew, Wai Loon.; Chen, Ken Shiung.	Journal Article
2011	UBE3A regulates MC1R expression : a link to hypopigmentation in Angelman Syndrome.	Low, Daren.; Chen, Ken Shiung.	Journal Article

Now showing items 1-6 of 6