X-Chromosome inactivation ratios affect wild-type MeCP2 expression within mosaic Rett syndrome and Mecp2 −/+ mouse brain

By Braunschweig Daniel   Simcox Thomas   Samaco Rodney C.   LaSalle Janine M.  

Human Molecular Genetics, Vol. 13, Iss. 12, 2004-06 ,pp. : 1275-1286

Oxford University Press

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Mouse models of MeCP2 disorders share gene expression changes in the cerebellum and hypothalamus

By Ben-Shachar Shay   Chahrour Maria   Thaller Christina   Shaw Chad A.   Zoghbi Huda Y.  

Human Molecular Genetics, Vol. 18, Iss. 13, 2009-07 ,pp. : 2431-2442

Oxford University Press

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MeCP2-dependent repression of an imprinted miR-184 released by depolarization

By Nomura Tasuku   Kimura Mika   Horii Takuro   Morita Sumiyo   Soejima Hidenobu   Kudo Shinichi   Hatada Izuho  

Human Molecular Genetics, Vol. 17, Iss. 8, 2008-04 ,pp. : 1192-1199

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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Elevated expression of MeCP2 in cardiac and skeletal tissues is detrimental for normal development

By Alvarez-Saavedra Matas   Carrasco Loreto   Sura-Trueba Sylvia   Demarchi Aiello Vera   Walz Katherina   Neto Jos Xavier   Young Juan I.  

Human Molecular Genetics, Vol. 19, Iss. 11, 2010-06 ,pp. : 2177-2190

Oxford University Press

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