X-Chromosome Inactivation in Rett Syndrome Human Induced Pluripotent Stem Cells

por Cheung, Aaron Y. L., Horvath, Lindsay M., Carrel, Laura, Ellis, James
Publicado 2012

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

por Cheung, Aaron Y.L., Horvath, Lindsay M., Grafodatskaya, Daria, Pasceri, Peter, Weksberg, Rosanna, Hotta, Akitsu, Carrel, Laura, Ellis, James
Publicado 2011

Over-Expression of Either MECP2_e1 or MECP2_e2 in Neuronally Differentiated Cells Results in Different Patterns of Gene Expression

por Orlic-Milacic, Marija, Kaufman, Liana, Mikhailov, Anna, Cheung, Aaron Y. L., Mahmood, Huda, Ellis, James, Gianakopoulos, Peter J., Minassian, Berge A., Vincent, John B.
Publicado 2014

MECP2 Isoform-Specific Vectors with Regulated Expression for Rett Syndrome Gene Therapy

por Rastegar, Mojgan, Hotta, Akitsu, Pasceri, Peter, Makarem, Maisam, Cheung, Aaron Y. L., Elliott, Shauna, Park, Katya J., Adachi, Megumi, Jones, Frederick S., Clarke, Ian D., Dirks, Peter, Ellis, James
Publicado 2009

MECP2e1 isoform mutation affects the form and function of neurons derived from Rett syndrome patient iPS cells

por Djuric, Ugljesa, Cheung, Aaron Y. L., Zhang, Wenbo, Mok, Rebecca S., Lai, Wesley, Piekna, Alina, Hendry, Jason A., Ross, P. Joel, Pasceri, Peter, Kim, Dae-Sung, Salter, Michael W., Ellis, James
Publicado 2015