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

Access to resources Recommend Favorite

MeCP2 in neurons: closing in on the causes of Rett Syndrome

By Caballero Isabel Martín   Hendrich Brian  

Human Molecular Genetics, Vol. 14, Iss. 14, 2005-07 ,pp. : 2089-2089

Oxford University Press

Access to resources Recommend Favorite

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

Access to resources Recommend Favorite

MECP2 mutations account for most cases of typical forms of Rett syndrome

By Bienvenu Thierry   Carrié Alain   de Nicolas  

Human Molecular Genetics, Vol. 9, Iss. 9, 2000-05 ,pp. : 1377-1384

Oxford University Press

Access to resources Recommend Favorite

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

Access to resources Recommend Favorite