المؤلفون: Simões de Oliveira, Laura^{Aff1, Aff2}, O’Leary, Heather E.^{Aff3, Aff8}, Nawaz, Sarfaraz^{Aff1, Aff2, Aff4, Aff5}, Loureiro, Rita^{Aff1, Aff2}, Davenport, Elizabeth C., Baxter, Paul^{Aff1, Aff6}, Louros, Susana R.^{Aff1, Aff2}, Dando, Owen^{Aff1, Aff2, Aff6}, Perkins, Emma^{Aff1, Aff2}, Peltier, Julien, Trost, Matthias, Osterweil, Emily K.^{Aff1, Aff2}, Hardingham, Giles E.^{Aff1, Aff2, Aff6}, Cousin, Michael A.^{Aff1, Aff2, Aff5}, Chattarji, Sumantra^{Aff1, Aff2, Aff4, Aff5}, Booker, Sam A.^{Aff1, Aff2}, Benke, Tim A.^{Aff3, Aff8, IDs13229024006019_cor17}, Wyllie, David J. A^{Aff1, Aff2, Aff5, Aff9, IDs13229024006019_cor18}, Kind, Peter C.^{Aff1, Aff2, Aff5, Aff9, IDs13229024006019_cor19}

المصدر: Molecular Autism. 15(1)

المؤلفون: 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.

المصدر: In Cell Reports 24 September 2024 43(9)

المؤلفون: Seo, Sang S.^{Aff1, Aff2}, Louros, Susana R.^{Aff1, Aff2}, Anstey, Natasha^{Aff1, Aff2}, Gonzalez-Lozano, Miguel A., Harper, Callista B.^{Aff1, Aff2}, Verity, Nicholas C.^{Aff1, Aff2}, Dando, Owen^{Aff1, Aff2}, Thomson, Sophie R.^{Aff1, Aff2}, Darnell, Jennifer C.^{Aff1, Aff2}, Kind, Peter C.^{Aff1, Aff2}, Li, Ka Wan, Osterweil, Emily K.^{Aff1, Aff2, IDs41467022309790_cor12}

المصدر: Nature Communications. 13(1)

المؤلفون: Elu, Nagore, Subash, Srividya, Louros, Susana R.

المصدر: Frontiers in Molecular Neuroscience; 2024, p1-8, 8p

مصطلحات موضوعية: ALTERNATIVE RNA splicing, FRAGILE X syndrome, RNA-binding proteins, GENETIC translation, POST-translational modification, RNA metabolism

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المؤلفون: 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.

المصدر: Thomson, S R, Seo, S S, Barnes, S A, Louros, S R, Muscas, M, Dando, O, Kirby, C, Wyllie, D J A, Hardingham, G E, Kind, P C & Osterweil, E K 2017, ' Cell-type-specific translation profiling reveals a novel strategy for treating fragile X syndrome ', Neuron, vol. 95, no. 3, pp. 550-563.e5 . https://doi.org/10.1016/j.neuron.2017.07.013

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______3094::01237cc91cf87ff55df1c32deddf67c9
https://hdl.handle.net/20.500.11820/fee3d084-b5f2-4569-9876-20df2b3a1147