Search Results - "Sgobio, C"

Abnormal medial prefrontal cortex connectivity and defective fear extinction in the presymptomatic G93A SOD1 mouse model of ALS by Sgobio, C., Trabalza, A., Spalloni, A., Zona, C., Carunchio, I., Longone, P., Ammassari‐Teule, M.

“…Amyotrophic lateral sclerosis (ALS) is a fatal progressive neuropathy associated with the degeneration of spinal and brainstem motor neurons. Although ALS is…”
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Postsynaptic alteration of NR2A subunit and defective autophosphorylation of alphaCaMKII at threonine-286 contribute to abnormal plasticity and morphology of upper motor neurons in presymptomatic SOD1G93A mice, a murine model for amyotrophic lateral sclerosis by Spalloni, A, Origlia, N, Sgobio, C, Trabalza, A, Nutini, M, Berretta, N, Bernardi, G, Domenici, L, Ammassari-Teule, M, Longone, P

“…Although amyotrophic lateral sclerosis (ALS) has long been considered as a lower motor neuron (MN) disease, degeneration of upper MNs arising from a…”
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Conditional Expression of Parkinson's Disease-Related Mutant  -Synuclein in the Midbrain Dopaminergic Neurons Causes Progressive Neurodegeneration and Degradation of Transcription Factor Nuclear Receptor Related 1 by Lin, X., Parisiadou, L., Sgobio, C., Liu, G., Yu, J., Sun, L., Shim, H., Gu, X.-L., Luo, J., Long, C.-X., Ding, J., Mateo, Y., Sullivan, P. H., Wu, L.-G., Goldstein, D. S., Lovinger, D., Cai, H.

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Landmark-based but not vestibular-based orientation elicits mossy fiber synaptogenesis in the mouse hippocampus by Middei, S., Vetere, G., Sgobio, C., Ammassari-Teule, M.

“…This study tries to shed light on the paradoxical finding that two inbred strains of mice C57BL/6 (C57) and DBA/2 (DBA), with differences in hippocampal…”
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Unbalanced calcium channel activity underlies selective vulnerability of nigrostriatal dopaminergic terminals in Parkinsonian mice by Sgobio, Carmelo, Sun, Lixin, Ding, Jinhui, Herms, Jochen, Lovinger, David M., Cai, Huaibin

“…Dopamine (DA) release in striatum is functionally segregated across a dorsolateral/ventromedial axis. Interestingly, nigrostriatal DA signaling disruption in…”
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Loss of Fragile X Mental Retardation Protein (FMRP) precedes Lewy pathology in Parkinson's Disease by Koeglsperger, T., Tan, Y., Sgobio, C., Arzberger, T., Machleid, F., Tang, Q., Findeis, E., Tost, J., Chakroun, T., Gao, P., Höllerhage, M., Bötzel, K., Herms, J., Höglinger, G.

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Distinct levels of dopamine denervation differentially alter striatal synaptic plasticity and NMDA receptor subunit composition by Paillé, Vincent, Picconi, Barbara, Bagetta, Vincenza, Ghiglieri, Veronica, Sgobio, Carmelo, Di Filippo, Massimiliano, Viscomi, Maria T, Giampà, Carmela, Fusco, Francesca R, Gardoni, Fabrizio, Bernardi, Giorgio, Greengard, Paul, Di Luca, Monica, Calabresi, Paolo

“…A correct interplay between dopamine (DA) and glutamate is essential for corticostriatal synaptic plasticity and motor activity. In an experimental model of…”
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Enriched Environment Promotes Behavioral and Morphological Recovery in a Mouse Model for the Fragile X Syndrome by Restivo, Leonardo, Ferrari, Francesca, Passino, Enrica, Sgobio, Carmelo, Bock, Jörg, Oostra, Ben A., Bagni, Claudia, Ammassari-Teule, Martine, Greenough, William T.

“…Fragile X syndrome, the most frequent form of hereditary mental retardation, is due to a mutation of the fragile X mental retardation 1 (FMR1) gene on the X…”
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Short-term and long-term plasticity at corticostriatal synapses: Implications for learning and memory by Di Filippo, Massimiliano, Picconi, Barbara, Tantucci, Michela, Ghiglieri, Veronica, Bagetta, Vincenza, Sgobio, Carmelo, Tozzi, Alessandro, Parnetti, Lucilla, Calabresi, Paolo

“…The striatum is the major division of the basal ganglia, representing the input station of the circuit and arguably the principal site within the basal ganglia…”
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Plastic and behavioral abnormalities in experimental Huntington's disease: A crucial role for cholinergic interneurons by Picconi, Barbara, Passino, Enrica, Sgobio, Carmelo, Bonsi, Paola, Barone, Ilaria, Ghiglieri, Veronica, Pisani, Antonio, Bernardi, Giorgio, Ammassari-Teule, Martine, Calabresi, Paolo

“…Huntington's disease (HD) is a fatal hereditary neurodegenerative disease causing degeneration of striatal spiny neurons, whereas cholinergic interneurons are…”
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Postsynaptic Alteration of NR2A Subunit and Defective Autophosphorylation of alphaCaMKII at Threonine-286 Contribute to Abnormal Plasticity and Morphology of Upper Motor Neurons in Presymptomatic SOD1 super(G93A) Mice, a Murine Model for Amyotrophic Lateral Sclerosis by Spalloni, A, Origlia, N, Sgobio, C, Trabalza, A, Nutini, M, Berretta, N, Bernardi, G, Domenici, L, Ammassari-Teule, M, Longone, P

“…Although amyotrophic lateral sclerosis (ALS) has long been considered as a lower motor neuron (MN) disease, degeneration of upper MNs arising from a…”
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Reversible inactivation of hippocampus and dorsolateral striatum in C57BL/6 and DBA/2 inbred mice failed to show interaction between memory systems in these genotypes by Middei, Silvia, Restivo, Leonardo, Sgobio, Carmelo, Passino, Enrica, Ammassari-Teule, Martine

“…C57BL/6 and DBA/2 mice with cannulae inserted bilaterally in the dorsal hippocampus or the dorsolateral striatum were released from the south arm of a cross…”
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