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

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A rare male patient with classic Rett syndrome caused by MeCP2_e1 mutation

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American Journal Of Medical Genetics Part A, Vol. 176, Iss. 3, 2018-03 ,pp. : 699-702

John Wiley & Sons Inc

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Inhibitors of differentiation (ID1, ID2, ID3 and ID4) genes are neuronal targets of MeCP2 that are elevated in Rett syndrome

By Peddada Sailaja   Yasui Dag H.   LaSalle Janine M.  

Human Molecular Genetics, Vol. 15, Iss. 12, 2006-06 ,pp. : 2003-2014

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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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

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