Crosstalk between ubiquitination and translation in neurodevelopmental disorders
Elu, Nagore, Subash, Srividya, R. Louros, Susana
Published in Frontiers in molecular neuroscience (02.09.2024)
Published in Frontiers in molecular neuroscience (02.09.2024)
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Sustained correction of associative learning deficits after brief, early treatment in a rat model of Fragile X Syndrome
Asiminas, Antonis, Jackson, Adam D, Louros, Susana R, Till, Sally M, Spano, Teresa, Dando, Owen, Bear, Mark F, Chattarji, Sumantra, Hardingham, Giles E, Osterweil, Emily K, Wyllie, David J A, Wood, Emma R, Kind, Peter C
Published in Science translational medicine (29.05.2019)
Published in Science translational medicine (29.05.2019)
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Journal Article
Cell-Type-Specific Translation Profiling Reveals a Novel Strategy for Treating Fragile X Syndrome
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.
Published in Neuron (Cambridge, Mass.) (02.08.2017)
Published in Neuron (Cambridge, Mass.) (02.08.2017)
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Journal Article
Excess ribosomal protein production unbalances translation in a model of Fragile X Syndrome
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
Published in Nature communications (10.06.2022)
Published in Nature communications (10.06.2022)
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Journal Article
A Role for Stargazin in Experience-Dependent Plasticity
Louros, Susana R., Hooks, Bryan M., Litvina, Liza, Carvalho, Ana Luisa, Chen, Chinfei
Published in Cell reports (Cambridge) (12.06.2014)
Published in Cell reports (Cambridge) (12.06.2014)
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Identification and functional modelling of plausibly causative cis-regulatory variants in a highly-selected cohort with X-linked intellectual disability
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
Published in PloS one (13.08.2021)
Published in PloS one (13.08.2021)
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Enhanced hippocampal LTP but normal NMDA receptor and AMPA receptor function in a rat model of CDKL5 deficiency disorder
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
Published in Molecular autism (14.06.2024)
Published in Molecular autism (14.06.2024)
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Excessive proteostasis contributes to pathology in fragile X syndrome
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.
Published in Neuron (Cambridge, Mass.) (15.02.2023)
Published in Neuron (Cambridge, Mass.) (15.02.2023)
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Journal Article
Ataxin-3 phosphorylation decreases neuronal defects in spinocerebellar ataxia type 3 models
Matos, Carlos A, Nóbrega, Clévio, Louros, Susana R, Almeida, Bruno, Ferreiro, Elisabete, Valero, Jorge, Pereira de Almeida, Luís, Macedo-Ribeiro, Sandra, Carvalho, Ana Luísa
Published in The Journal of cell biology (15.02.2016)
Published in The Journal of cell biology (15.02.2016)
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Key roles of C2/GAP domains in SYNGAP1-related pathophysiology
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.
Published in Cell reports (Cambridge) (24.09.2024)
Published in Cell reports (Cambridge) (24.09.2024)
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Journal Article
Identification and functional modelling of plausibly causative cis-regulatory variants in a highly-selected cohort with X-linked intellectual disability
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
Published in PloS one (2021)
Published in PloS one (2021)
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Journal Article
Excess ribosomal protein production unbalances translation in Fragile X Syndrome
Seo, Sang S, Louros, Susana R, Anstey, Natasha, Gonzalez-Lazano, Miguel A, Thomson, Sophie R, Harper, Callista, Verity, Nicholas, Darnell, Jennifer C, Ka Wan Li, Kind, Peter C, Osterweil, Emily K
Published in bioRxiv (08.04.2022)
Published in bioRxiv (08.04.2022)
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