The Role of MeCP2 in the Brain von Guy, Jacky, Cheval, Hélène, Selfridge, Jim, Bird, Adrian

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Reversal of Neurological Defects in a Mouse Model of Rett Syndrome von Guy, Jacky, Gan, Jian, Selfridge, Jim, Cobb, Stuart, Bird, Adrian

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Fingolimod, a sphingosine-1 phosphate receptor modulator, increases BDNF levels and improves symptoms of a mouse model of Rett syndrome von Deogracias, Rubén, Yazdani, Morteza, Dekkers, Martijn P. J, Guy, Jacky, Ionescu, Mihai Constantin S, Vogt, Kaspar E, Barde, Yves-Alain

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Cell type-specific DNA methylation at intragenic CpG islands in the immune system von Deaton, Aimée M, Webb, Shaun, Kerr, Alastair R W, Illingworth, Robert S, Guy, Jacky, Andrews, Robert, Bird, Adrian

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CpG islands influence chromatin structure via the CpG-binding protein Cfp1 von Thomson, John P., Skene, Peter J., Selfridge, Jim, Clouaire, Thomas, Guy, Jacky, Webb, Shaun, Kerr, Alastair R. W., Deaton, Aimée, Andrews, Rob, James, Keith D., Turner, Daniel J., Illingworth, Robert, Bird, Adrian

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

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A mutation-led search for novel functional domains in MeCP2 von Guy, Jacky, Alexander-Howden, Beatrice, FitzPatrick, Laura, DeSousa, Dina, Koerner, Martha V, Selfridge, Jim, Bird, Adrian

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Disease Modeling Using Embryonic Stem Cells: MeCP2 Regulates Nuclear Size and RNA Synthesis in Neurons von Yazdani, Morteza, Deogracias, Rubén, Guy, Jacky, Poot, Raymond A., Bird, Adrian, Barde, Yves-Alain

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Identifying proteins bound to native mitotic ESC chromosomes reveals chromatin repressors are important for compaction von Djeghloul, Dounia, Patel, Bhavik, Kramer, Holger, Dimond, Andrew, Whilding, Chad, Brown, Karen, Kohler, Anne-Céline, Feytout, Amelie, Veland, Nicolas, Elliott, James, Bharat, Tanmay A. M., Tarafder, Abul K., Löwe, Jan, Ng, Bee L., Guo, Ya, Guy, Jacky, Huseyin, Miles K., Klose, Robert J., Merkenschlager, Matthias, Fisher, Amanda G.

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Gene Expression Analysis Exposes Mitochondrial Abnormalities in a Mouse Model of Rett Syndrome von Kriaucionis, Skirmantas, Paterson, Andrew, Curtis, John, Guy, Jacky, MacLeod, Nikki, Bird, Adrian

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Affinity for DNA Contributes to NLS Independent Nuclear Localization of MeCP2 von Lyst, Matthew J., Ekiert, Robert, Guy, Jacky, Selfridge, Jim, Koerner, Martha V., Merusi, Cara, De Sousa, Dina, Bird, Adrian

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

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Comparative analysis of potential broad-spectrum neuronal Cre drivers von Paton, Katie M, Selfridge, Jim, Guy, Jacky, Bird, Adrian

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Up-regulation of glucocorticoid-regulated genes in a mouse model of Rett syndrome von Nuber, Ulrike A., Kriaucionis, Skirmantas, Roloff, Tim C., Guy, Jacky, Selfridge, Jim, Steinhoff, Christine, Schulz, Ralph, Lipkowitz, Bettina, Ropers, H. Hilger, Holmes, Megan C., Bird, Adrian

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Enhanced CpG Mutability and Tumorigenesis in MBD4-Deficient Mice von Millar, Catherine B., Guy, Jacky, Sansom, Owen J., Selfridge, Jim, MacDougall, Eilidh, Hendrich, Brian, Keightley, Peter D., Bishop, Stefan M., Clarke, Alan R., Bird, Adrian

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Abnormal N-glycosylation pattern for brain nucleotide pyrophosphatase-5 (NPP-5) in Mecp2-mutant murine models of Rett syndrome von Cortelazzo, Alessio, De Felice, Claudio, Guerranti, Roberto, Signorini, Cinzia, Leoncini, Silvia, Pecorelli, Alessandra, Scalabrì, Francesco, Madonna, Michele, Filosa, Stefania, Della Giovampaola, Cinzia, Capone, Antonietta, Durand, Thierry, Mirasole, Cristiana, Zolla, Lello, Valacchi, Giuseppe, Ciccoli, Lucia, Guy, Jacky, D’Esposito, Maurizio, Hayek, Joussef

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Radically truncated MeCP2 rescues Rett syndromelike neurological defects von Tillotson, Rebekah, Selfridge, Jim, Koerner, Martha V, Gadalla, Kamal K E, Guy, Jacky, De Sousa, Dina, Hector, Ralph D, Cobb, Stuart R, Bird, Adrian

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In vivo Transposition of Minos, A Drosophila Mobile Element, in Mammalian Tissues von Zagoraiou, Laskaro, Drabek, Dubravka, Alexaki, Sofia, Guy, Jacky A., Klinakis, Apostolos G., Langeveld, An, Skavdis, George, Mamalaki, Clio, Grosveld, Frank, Savakis, Charalambos

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Radically truncated MeCP2 rescues Rett syndrome-like neurological defects von Tillotson, Rebekah, Selfridge, Jim, Koerner, Martha V., Gadalla, Kamal K. E., Guy, Jacky, De Sousa, Dina, Hector, Ralph D., Cobb, Stuart R., Bird, Adrian

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Rett syndrome mutations abolish the interaction of MeCP2 with the NCoR/SMRT co-repressor von Lyst, Matthew J, Ekiert, Robert, Ebert, Daniel H, Merusi, Cara, Nowak, Jakub, Selfridge, Jim, Guy, Jacky, Kastan, Nathaniel R, Robinson, Nathaniel D, de Lima Alves, Flavia, Rappsilber, Juri, Greenberg, Michael E, Bird, Adrian

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