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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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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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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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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CDKL5 belongs to the same molecular pathway of MeCP2 and it is responsible for the early-onset seizure variant of Rett syndrome

By Mari Francesca  

Human Molecular Genetics, Vol. 14, Iss. 14, 2005-07 ,pp. : 1935-1946

Oxford University Press

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