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European Journal of Human Genetics : EJHG|June 24, 2010
Genome-wide gene expression profiling of the Angelman syndrome mice with Ube3a mutationDaren Low, Ken-Shiung ChenPigment Cell & Melanoma Research|July 8, 2011
UBE3A regulates MC1R expression: a link to hypopigmentation in Angelman syndromeDaren Low, Ken-Shiung ChenBMC Molecular Biology|January 21, 2011
Rasd1 interacts with Ear2 (Nr2f6) to regulate renin transcriptionJen Jen Tan, Shufen Angeline Ong, Ken-Shiung ChenPlos One|September 15, 2011
Rasd1 modulates the coactivator function of NonO in the cyclic AMP pathwayShufen Angeline Ong, Jen Jen Tan, Wai Loon Tew, et al.Human Molecular Genetics|June 21, 2002
Evidence for translational regulation of the imprinted Snurf-Snrpn locus in miceTing-Fen Tsai, Ken-Shiung Chen, John S Weber, et al.Genesis (New York, N.Y. : 2000)|January 7, 2006
Mouse imprinting defect mutations that model Angelman syndromeMei-Yi Wu, Ken-Shiung Chen, Jan Bressler, et al.Journal of Neurophysiology|April 8, 2011
NMDA receptor activation enhances inhibitory GABAergic transmission onto hippocampal pyramidal neurons via presynaptic and postsynaptic mechanismsJiu-Gang Xue, Takayoshi Masuoka, Xian-Di Gong, et al.Annals of Human Genetics|January 5, 2011
Genetic studies of Prader-Willi patients provide evidence for conservation of genomic architecture in proximal chromosome 15qAihua Hou, Shuan-Pei Lin, Shi Yun Ho, et al.Molecular and Cellular Biology|April 25, 2002
Fliih, a gelsolin-related cytoskeletal regulator essential for early mammalian embryonic developmentHugh D Campbell, Shelley Fountain, Ian S McLennan, et al.Pageof 1