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

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

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

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

The MeCP2/YY1 interaction regulates ANT1 expression at 4q35: novel hints for Rett syndrome pathogenesis

By Forlani Greta   Giarda Elisa   Ala Ugo   Di Cunto Ferdinando   Salani Monica   Tupler Rossella   Kilstrup-Nielsen Charlotte   Landsberger Nicoletta  

Human Molecular Genetics, Vol. 19, Iss. 16, 2010-08 ,pp. : 3114-3123

Oxford University Press

Access to resources Recommend Favorite