Claudia Bagni

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"Claudia Bagni"
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Publications

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Jacquemont S, Pacini L, Jønch AE, et al. (2018) Protein synthesis levels are increased in a subset of individuals with fragile X syndrome. Human Molecular Genetics
Jacquemont S, Pacini L, Jønch AE, et al. (2018) Protein synthesis levels are increased in a subset of individuals with Fragile X syndrome. Human Molecular Genetics
Yrigollen CM, Pacini L, Nobile V, et al. (2016) Clinical and Molecular Assessment in a Female with Fragile X Syndrome and Tuberous Sclerosis. Journal of Genetic Disorders & Genetic Reports. 5
Stepniak B, Kästner A, Poggi G, et al. (2015) Accumulated common variants in the broader fragile X gene family modulate autistic phenotypes. Embo Molecular Medicine
Di Marino D, Chillemi G, De Rubeis S, et al. (2015) MD and Docking Studies Reveal That the Functional Switch of CYFIP1 is Mediated by a Butterfly-like Motion. Journal of Chemical Theory and Computation. 11: 3401-10
Grant SG, Bagni C, O'Dell TJ. (2015) Synaptopathy - From Biology to Therapy. Neuropharmacology
Pasciuto E, Borrie SC, Kanellopoulos AK, et al. (2015) Autism Spectrum Disorders: Translating human deficits into mouse behavior. Neurobiology of Learning and Memory. 124: 71-87
Pasciuto E, Ahmed T, Wahle T, et al. (2015) Dysregulated ADAM10-Mediated Processing of APP during a Critical Time Window Leads to Synaptic Deficits in Fragile X Syndrome. Neuron. 87: 382-98
Fernández E, Li KW, Rajan N, et al. (2015) FXR2P Exerts a Positive Translational Control and Is Required for the Activity-Dependent Increase of PSD95 Expression. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 35: 9402-8
Di Marino D, D'Annessa I, Tancredi H, et al. (2015) A unique binding mode of the eukaryotic translation initiation factor 4E for guiding the design of novel peptide inhibitors. Protein Science : a Publication of the Protein Society. 24: 1370-82
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