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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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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FXYD1 is an MeCP2 target gene overexpressed in the brains of Rett syndrome patients and Mecp2-null mice

By Deng Vivianne   Matagne Valerie   Frerking Matthew   Ohliger Patricia   Budden Sarojini   Pevsner Jonathan   Dissen Gregory A.   Sherman Larry S.   Ojeda Sergio R.  

Human Molecular Genetics, Vol. 16, Iss. 6, 2007-03 ,pp. : 640-650

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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Age-dependent expression of MeCP2 in a heterozygous mosaic mouse model

By Smrt Richard D.   Pfeiffer Rebecca L.   Zhao Xinyu  

Human Molecular Genetics, Vol. 20, Iss. 9, 2011-05 ,pp. : 1834-1843

Oxford University Press

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