Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3

By Samaco Rodney C.   Hogart Amber   LaSalle Janine M.  

Human Molecular Genetics, Vol. 14, Iss. 4, 2005-02 ,pp. : 483-492

Oxford University Press

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MeCP2 deficiency in Rett syndrome causes epigenetic aberrations at the PWS/AS imprinting center that affects UBE3A expression

By Makedonski Kirill   Abuhatzira Liron   Kaufman Yotam   Razin Aharon   Shemer Ruth  

Human Molecular Genetics, Vol. 14, Iss. 8, 2005-04 ,pp. : 1049-1058

Oxford University Press

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Expression of the Rho-GEF Pbl/ECT2 is regulated by the UBE3A E3 ubiquitin ligase

By Reiter Lawrence T.   Seagroves Tiffany N.   Bowers Megan   Bier Ethan  

Human Molecular Genetics, Vol. 15, Iss. 18, 2006-09 ,pp. : 2825-2835

Oxford University Press

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Identification of cis-regulatory elements for MECP2 expression

By Liu Jinglan   Francke Uta  

Human Molecular Genetics, Vol. 15, Iss. 11, 2006-06 ,pp. : 1769-1782

Oxford University Press

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Ube3a-ATS is an atypical RNA polymerase II transcript that represses the paternal expression of Ube3a

By Meng Linyan   Person Richard E.   Beaudet Arthur L.  

Human Molecular Genetics, Vol. 21, Iss. 13, 2012-07 ,pp. : 3001-3012

Oxford University Press

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