Isolation of MECP2 -null Rett Syndrome patient hiPS cells and isogenic controls through X-chromosome inactivation

By Cheung Aaron Y.L.   Horvath Lindsay M.   Grafodatskaya Daria   Pasceri Peter   Weksberg Rosanna   Hotta Akitsu   Carrel Laura   Ellis James  

Human Molecular Genetics, Vol. 20, Iss. 11, 2011-06 ,pp. : 2103-2115

Oxford University Press

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Age-dependent expression of MeCP2 in a heterozygous mosaic mouse model

By Smrt Richard D.   Pfeiffer Rebecca L.   Zhao Xinyu  

Human Molecular Genetics, Vol. 20, Iss. 9, 2011-05 ,pp. : 1834-1843

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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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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