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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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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Quantitative localization of heterogeneous methyl-CpG-binding protein 2 (MeCP2) expression phenotypes in normal and Rett syndrome brain by laser scanning cytometry

By Greco C.M.   LaSalle J.M.   Goldstine J.   Balmer D.  

Human Molecular Genetics, Vol. 10, Iss. 17, 2001-08 ,pp. : 1729-1740

Oxford University Press

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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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