The molecular basis of variable phenotypic severity among common missense mutations causing Rett syndrome

by Brown, Kyla, Selfridge, Jim, Lagger, Sabine, Connelly, John, De Sousa, Dina, Kerr, Alastair, Webb, Shaun, Guy, Jacky, Merusi, Cara, Koerner, Martha V., Bird, Adrian
Published 2016

DNA methylation reader MECP2: cell type- and differentiation stage-specific protein distribution

by Song, Congdi, Feodorova, Yana, Guy, Jacky, Peichl, Leo, Jost, Katharina Laurence, Kimura, Hiroshi, Cardoso, Maria Cristina, Bird, Adrian, Leonhardt, Heinrich, Joffe, Boris, Solovei, Irina
Published 2014

Preclinical research in Rett syndrome: setting the foundation for translational success

by Katz, David M., Berger-Sweeney, Joanne E., Eubanks, James H., Justice, Monica J., Neul, Jeffrey L., Pozzo-Miller, Lucas, Blue, Mary E., Christian, Diana, Crawley, Jacqueline N., Giustetto, Maurizio, Guy, Jacky, Howell, C. James, Kron, Miriam, Nelson, Sacha B., Samaco, Rodney C., Schaevitz, Laura R., St. Hillaire-Clarke, Coryse, Young, Juan L., Zoghbi, Huda Y., Mamounas, Laura A.
Published 2012

Oxidative brain damage in Mecp2-mutant murine models of Rett syndrome

by De Felice, Claudio, Della Ragione, Floriana, Signorini, Cinzia, Leoncini, Silvia, Pecorelli, Alessandra, Ciccoli, Lucia, Scalabrì, Francesco, Marracino, Federico, Madonna, Michele, Belmonte, Giuseppe, Ricceri, Laura, De Filippis, Bianca, Laviola, Giovanni, Valacchi, Giuseppe, Durand, Thierry, Galano, Jean-Marie, Oger, Camille, Guy, Alexandre, Bultel-Poncé, Valérie, Guy, Jacky, Filosa, Stefania, Hayek, Joussef, D'Esposito, Maurizio
Published 2014