Francesco Longo
Affiliations: | NYU CNS, New York, NY, United States |
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Parents
Sign in to add mentorMichele Morari | grad student | 2011-2015 | (FlyTree) |
Eric Klann | post-doc | 2015- |
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Publications
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Busch SE, Simmons DH, Gama E, et al. (2023) Overexpression of the autism candidate gene pathologically enhances olivo-cerebellar signaling in mice. Frontiers in Cellular Neuroscience. 17: 1219270 |
Longo F, Aryal S, Anastasiades PG, et al. (2023) Cell-type-specific disruption of cortico-striatal circuitry drives repetitive patterns of behavior in fragile X syndrome model mice. Cell Reports. 42: 112901 |
Mercaldo V, Vidimova B, Gastaldo D, et al. (2023) Altered striatal actin dynamics drives behavioral inflexibility in a mouse model of fragile X syndrome. Neuron |
Kalinowska M, van der Lei MB, Kitiashvili M, et al. (2022) Deletion of Fmr1 in parvalbumin-expressing neurons results in dysregulated translation and selective behavioral deficits associated with fragile X syndrome. Molecular Autism. 13: 29 |
Gross C, Banerjee A, Tiwari D, et al. (2022) Correction to: Isoform-selective phosphoinositide 3-kinase inhibition ameliorates a broad range of fragile X syndrome-associated deficits in a mouse model. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology |
Allen M, Huang BS, Notaras MJ, et al. (2022) Spontaneous generation of ASD astrocytes. Molecular Psychiatry. 27: 2369 |
Allen M, Huang BS, Notaras MJ, et al. (2022) Astrocytes derived from ASD individuals alter behavior and destabilize neuronal activity through aberrant Ca signaling. Molecular Psychiatry |
Viaro R, Longo F, Vincenzi F, et al. (2021) L-DOPA promotes striatal dopamine release through D1 receptors and reversal of dopamine transporter. Brain Research. 147583 |
Longo F, Klann E. (2021) Reciprocal control of translation and transcription in autism spectrum disorder. Embo Reports. e52110 |
Aryal S, Longo F, Klann E. (2021) Genetic removal of p70 S6K1 corrects coding sequence length-dependent alterations in mRNA translation in fragile X syndrome mice. Proceedings of the National Academy of Sciences of the United States of America. 118 |