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

by Cheung, Aaron Y. L., Horvath, Lindsay M., Carrel, Laura, Ellis, James
Published 2012

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
Published 2011

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

by 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
Published 2009

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

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

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

by 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
Published 2015