Crosstalk between ubiquitination and translation in neurodevelopmental disorders von Elu, Nagore, Subash, Srividya, R Louros, Susana

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Cell-Type-Specific Translation Profiling Reveals a Novel Strategy for Treating Fragile X Syndrome von Thomson, Sophie R., Seo, Sang S., Barnes, Stephanie A., Louros, Susana R., Muscas, Melania, Dando, Owen, Kirby, Caoimhe, Wyllie, David J.A., Hardingham, Giles E., Kind, Peter C., Osterweil, Emily K.

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Excess ribosomal protein production unbalances translation in a model of Fragile X Syndrome von Seo, Sang S., Louros, Susana R., Anstey, Natasha, Gonzalez-Lozano, Miguel A., Harper, Callista B., Verity, Nicholas C., Dando, Owen, Thomson, Sophie R., Darnell, Jennifer C., Kind, Peter C., Li, Ka Wan, Osterweil, Emily K.

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A Role for Stargazin in Experience-Dependent Plasticity von Louros, Susana R., Hooks, Bryan M., Litvina, Liza, Carvalho, Ana Luisa, Chen, Chinfei

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Identification and functional modelling of plausibly causative cis-regulatory variants in a highly-selected cohort with X-linked intellectual disability von Bengani, Hemant, Grozeva, Detelina, Moyon, Lambert, Bhatia, Shipra, Louros, Susana R., Hope, Jilly, Jackson, Adam, Prendergast, James G., Owen, Liusaidh J., Naville, Magali, Rainger, Jacqueline, Grimes, Graeme, Halachev, Mihail, Murphy, Laura C., Spasic-Boskovic, Olivera, van Heyningen, Veronica, Kind, Peter, Abbott, Catherine M., Osterweil, Emily, Raymond, F. Lucy, Crollius, Hugues Roest, FitzPatrick, David R.

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Stargazin Dephosphorylation Mediates Homeostatic Synaptic Downscaling of Excitatory Synapses von Louros, Susana R, Caldeira, Gladys L, Carvalho, Ana Luísa

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Enhanced hippocampal LTP but normal NMDA receptor and AMPA receptor function in a rat model of CDKL5 deficiency disorder von Simões de Oliveira, Laura, O'Leary, Heather E, Nawaz, Sarfaraz, Loureiro, Rita, Davenport, Elizabeth C, Baxter, Paul, Louros, Susana R, Dando, Owen, Perkins, Emma, Peltier, Julien, Trost, Matthias, Osterweil, Emily K, Hardingham, Giles E, Cousin, Michael A, Chattarji, Sumantra, Booker, Sam A, Benke, Tim A, Wyllie, David J A, Kind, Peter C

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Perturbed proteostasis in autism spectrum disorders von Louros, Susana R., Osterweil, Emily K.

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Excessive proteostasis contributes to pathology in fragile X syndrome von Louros, Susana R., Seo, Sang S., Maio, Beatriz, Martinez-Gonzalez, Cristina, Gonzalez-Lozano, Miguel A., Muscas, Melania, Verity, Nick C., Wills, Jimi C., Li, Ka Wan, Nolan, Matthew F., Osterweil, Emily K.

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Lovastatin, not Simvastatin, Corrects Core Phenotypes in the Fragile X Mouse Model von Muscas, Melania, Louros, Susana R, Osterweil, Emily K

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Ataxin-3 phosphorylation decreases neuronal defects in spinocerebellar ataxia type 3 models von Matos, Carlos A, Nóbrega, Clévio, Louros, Susana R, Almeida, Bruno, Ferreiro, Elisabete, Valero, Jorge, Pereira de Almeida, Luís, Macedo-Ribeiro, Sandra, Carvalho, Ana Luísa

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Key roles of C2/GAP domains in SYNGAP1-related pathophysiology von Katsanevaki, Danai, Till, Sally M., Buller-Peralta, Ingrid, Nawaz, Mohammad Sarfaraz, Louros, Susana R., Kapgal, Vijayakumar, Tiwari, Shashank, Walsh, Darren, Anstey, Natasha J., Petrović, Nina G., Cormack, Alison, Salazar-Sanchez, Vanesa, Harris, Anjanette, Farnworth-Rowson, William, Sutherland, Andrew, Watson, Thomas C., Dimitrov, Siyan, Jackson, Adam D., Arkell, Daisy, Biswal, Suryanarayan, Dissanayake, Kosala N., Mizen, Lindsay A.M., Perentos, Nikolas, Jones, Matt W., Cousin, Michael A., Booker, Sam A., Osterweil, Emily K., Chattarji, Sumantra, Wyllie, David J.A., Gonzalez-Sulser, Alfredo, Hardt, Oliver, Wood, Emma R., Kind, Peter C.

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A Differential Effect of Lovastatin versus Simvastatin in Neurodevelopmental Disorders von Muscas, Melania, Seo, Sang S., Louros, Susana R., Osterweil, Emily K.

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Identification and functional modelling of plausibly causative cis-regulatory variants in a highly-selected cohort with X-linked intellectual disability von Bengani, Hemant, Grozeva, Detelina, Moyon, Lambert, Bhatia, Shipra, Louros, Susana R, Hope, Jilly, Jackson, Adam, Prendergast, James G, Owen, Liusaidh J, Naville, Magali, Rainger, Jacqueline, Grimes, Graeme, Halachev, Mihail, Murphy, Laura C, Spasic-Boskovic, Olivera, van Heyningen, Veronica, Kind, Peter, Abbott, Catherine M., Osterweil, Emily, Raymond, F. Lucy, Crollius, Roest, Fitzpatrick, David R

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Identification and functional modelling of plausibly causative cis-regulatory variants in a highly-selected cohort with X-linked intellectual disability von Bengani, Hemant, Grozeva, Detelina, Moyon, Lambert, Bhatia, Shipra, Louros, Susana R, Hope, Jilly, Jackson, Adam, Prendergast, James G, Owen, Liusaidh J, Naville, Magali, Rainger, Jacqueline, Grimes, Graeme, Halachev, Mihail, Murphy, Laura C, Spasic-Boskovic, Olivera, van Heyningen, Veronica, Kind, Peter, Abbott, Catherine M, Osterweil, Emily, Raymond, F Lucy, Crollius, Hugues Roest, FitzPatrick, David R

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Identification and functional modelling of plausibly causative cis -regulatory variants in a highly-selected cohort with X-linked intellectual disability von Bengani, Hemant, Grozeva, Detelina, Moyon, Lambert, Bhatia, Shipra, Louros, Susana R, Hope, Jilly, Jackson, Adam, Prendergast, James G, Owen, Liusaidh J, Naville, Magali, Rainger, Jacqueline, Grimes, Graeme, Halachev, Mihail, Murphy, Laura C, Spasic-Boskovic, Olivera, van Heyningen, Veronica, Kind, Peter, Abbott, Catherine M, Osterweil, Emily, Raymond, F. Lucy, Roest Crollius, Hugues, FitzPatrick, David R

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Identification and functional modelling of plausibly causative cis-regulatory variants in a highly-selected cohort with X-linked intellectual disability von Bengani, Hemant, Grozeva, Detelina, Moyon, Lambert, Bhatia, Shipra, Louros, Susana R, Hope, Jilly, Jackson, Adam, Prendergast, James G, Owen, Liusaidh J, Naville, Magali, Rainger, Jacqueline, Grimes, Graeme, Halachev, Mihail, Murphy, Laura C, Spasic-Boskovic, Olivera, van Heyningen, Veronica, Kind, Peter, Abbott, Catherine M, Osterweil, Emily, Raymond, F Lucy, Roest Crollius, Hugues, FitzPatrick, David R

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Additional file 3 of Enhanced hippocampal LTP but normal NMDA receptor and AMPA receptor function in a rat model of CDKL5 deficiency disorder von Simões de Oliveira, Laura, O’Leary, Heather E., Nawaz, Sarfaraz, Loureiro, Rita, Davenport, Elizabeth C., Baxter, Paul, Louros, Susana R., Dando, Owen, Perkins, Emma, Peltier, Julien, Trost, Matthias, Osterweil, Emily K., Hardingham, Giles E., Cousin, Michael A., Chattarji, Sumantra, Booker, Sam A., Benke, Tim A., Wyllie, David J. A, Kind, Peter C.

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Additional file 5 of Enhanced hippocampal LTP but normal NMDA receptor and AMPA receptor function in a rat model of CDKL5 deficiency disorder von Simões de Oliveira, Laura, O’Leary, Heather E., Nawaz, Sarfaraz, Loureiro, Rita, Davenport, Elizabeth C., Baxter, Paul, Louros, Susana R., Dando, Owen, Perkins, Emma, Peltier, Julien, Trost, Matthias, Osterweil, Emily K., Hardingham, Giles E., Cousin, Michael A., Chattarji, Sumantra, Booker, Sam A., Benke, Tim A., Wyllie, David J. A, Kind, Peter C.

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Additional file 2 of Enhanced hippocampal LTP but normal NMDA receptor and AMPA receptor function in a rat model of CDKL5 deficiency disorder von Simões de Oliveira, Laura, O’Leary, Heather E., Nawaz, Sarfaraz, Loureiro, Rita, Davenport, Elizabeth C., Baxter, Paul, Louros, Susana R., Dando, Owen, Perkins, Emma, Peltier, Julien, Trost, Matthias, Osterweil, Emily K., Hardingham, Giles E., Cousin, Michael A., Chattarji, Sumantra, Booker, Sam A., Benke, Tim A., Wyllie, David J. A, Kind, Peter C.

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