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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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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MeCP2 involvement in the regulation of neuronal -tubulin production

By Abuhatzira Liron   Shemer Ruth   Razin Aharon  

Human Molecular Genetics, Vol. 18, Iss. 8, 2009-04 ,pp. : 1415-1423

Oxford University Press

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MeCP2 Rett mutations affect large scale chromatin organization

By Agarwal Noopur   Becker Annette   Jost K. Laurence   Haase Sebastian   Thakur Basant K.   Brero Alessandro   Hardt Tanja   Kudo Shinichi   Leonhardt Heinrich   Cardoso M. Cristina  

Human Molecular Genetics, Vol. 20, Iss. 21, 2011-11 ,pp. : 4187-4195

Oxford University Press

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