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Journal of Cellular Biochemistry|March 22, 2005
Imprinting centers, chromatin structure, and diseaseHidenobu Soejima, Joseph WagstaffAmerican Journal of Medical Genetics. Part A|July 16, 2008
Mechanisms of imprinting of the Prader-Willi/Angelman regionBernhard Horsthemke, Joseph WagstaffNeurobiology of Disease|June 1, 2005
Sleep disturbances in Ube3a maternal-deficient mice modeling Angelman syndromeDamien Colas, Joseph Wagstaff, Patrice Fort, et al.Annals of the New York Academy of Sciences|January 22, 2005
From electrophysiology to chromatin: a bottom-up approach to Angelman syndromeBernard Dan, Laurent Servais, Stewart G Boyd, et al.The Journal of Biological Chemistry|February 15, 2003
Role of histone methyltransferase G9a in CpG methylation of the Prader-Willi syndrome imprinting centerZhenghan Xin, Makoto Tachibana, Michele Guggiari, et al.The Journal of Biological Chemistry|July 21, 2004
Biochemical analysis of Angelman syndrome-associated mutations in the E3 ubiquitin ligase E6-associated proteinEric M Cooper, Amy W Hudson, Joseph Amos, et al.Nucleic Acids Research|July 20, 2005
Maternal disruption of Ube3a leads to increased expression of Ube3a-ATS in transMiguel Landers, Margaret A Calciano, Dan Colosi, et al.Neurobiology of Disease|March 16, 2002
Neurobehavioral and electroencephalographic abnormalities in Ube3a maternal-deficient miceKiyonori Miura, Tatsuya Kishino, En Li, et al.Human Genetics|March 12, 2004
SNURF-SNRPN and UBE3A transcript levels in patients with Angelman syndromeMaren Runte, Peter M Kroisel, Gabriele Gillessen-Kaesbach, et al.American Journal of Medical Genetics. Part A|February 14, 2006
Angelman syndrome 2005: updated consensus for diagnostic criteriaCharles A Williams, Arthur L Beaudet, Jill Clayton-Smith, et al.Pageof 2