Multiple pathways regulate MeCP2 expression in normal brain development and exhibit defects in autism-spectrum disorders

By Samaco Rodney C.   Nagarajan Raman P.   Braunschweig Daniel   LaSalle Janine M.  

Human Molecular Genetics, Vol. 13, Iss. 6, 2004-03 ,pp. : 629-639

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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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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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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