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Giovanni Lugli

Researcher at University of Illinois at Chicago

Publications -  19
Citations -  1917

Giovanni Lugli is an academic researcher from University of Illinois at Chicago. The author has contributed to research in topics: Dendritic spine & Synaptic plasticity. The author has an hindex of 15, co-authored 19 publications receiving 1701 citations.

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Plasma Exosomal miRNAs in Persons with and without Alzheimer Disease: Altered Expression and Prospects for Biomarkers

TL;DR: The findings warrant replication and follow-up with a larger cohort of patients and controls who have been carefully characterized in terms of cognitive and imaging data, other biomarkers and risk factors, and who are sampled repeatedly over time.
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MicroRNA expression is down-regulated and reorganized in prefrontal cortex of depressed suicide subjects

TL;DR: Overall miRNA expression was significantly and globally down-regulated in prefrontal cortex of depressed suicide subjects, and a set of 29 miRNAs showed a high degree of co-regulation across individuals in the depressed suicide group.
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Dicer and eIF2c are enriched at postsynaptic densities in adult mouse brain and are modified by neuronal activity in a calpain‐dependent manner

TL;DR: The findings support a model whereby acute neuronal stimulation at excitatory synapses increases intracellular calcium, which activates calpain, which liberates dicer and eIF2c bound to PSDs, which supports the hypothesis that dicer could be involved in synaptic plasticity.
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Expression of microRNAs and their Precursors in Synaptic Fractions of Adult Mouse Forebrain

TL;DR: Findings support the proposal that microRNAs are formed, at least in part, via processing of microRNA precursors locally within dendritic spines via synaptic stimulation in proximity to the synapse.
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Expression of microRNAs and Other Small RNAs in Prefrontal Cortex in Schizophrenia, Bipolar Disorder and Depressed Subjects

TL;DR: There was a significant inverse correlation between the fold-change of a given miRNA seen in schizophrenia and its synaptic enrichment ratio observed in controls, suggesting some deficit in miRNA biogenesis, transport, processing or turnover in schizophrenia that is selective for the synaptic compartment.