Progetto di un Palazzetto dello Sport nel Comune di Carrara

Durante il lavoro di tes si sono studiate le piante della struttura la disposizione interna degli spazi e soprattutto la copertura della struttura con i relativi particolari costruttivi

L'apprendista nel mercato del lavoro

Il presente elaborato, ripercorre, per sommi capi, l'evoluzione dell'istituto dal periodo medioevale sino al Testo Unico del 2011 mettendo in evidenza gli interventi che ad avviso di chi scrive hanno modificato profondamente il contratto

Experimental demonstration of Continuous-Variable Quantum Key Distribution with a silicon photonics integrated receiver

Quantum Key Distribution (QKD) is a prominent application in the field of quantum cryptography providing information-theoretic security for secret key exchange. The implementation of QKD systems on photonic integrated circuits (PICs) can reduce the size and cost of such systems and facilitate their deployment in practical infrastructures. To this end, continuous-variable (CV) QKD systems are particularly well-suited as they do not require single-photon detectors, whose integration is presently challenging. Here we present a CV-QKD receiver based on a silicon PIC capable of performing balanced detection. We characterize its performance in a laboratory QKD setup using a frequency multiplexed pilot scheme with specifically designed data processing allowing for high modulation and secret key rates. The obtained excess noise values are compatible with asymptotic secret key rates of 2.4 Mbit/s and 220 kbit/s at an emulated distance of 10 km and 23 km, respectively. These results demonstrate the potential of this technology towards fully integrated devices suitable for high-speed, metropolitan-distance secure communication.Comment: 11 pages, 13 figures; Changed figure 8, acknowledgments update

Connecting Quantum Cities: Simulation of a Satellite-Based Quantum Network

We present and analyse an architecture for a European-scale quantum network using satellite links to connect Quantum Cities, which are metropolitan quantum networks with minimal hardware requirements for the end users. Using NetSquid, a quantum network simulation tool based on discrete events, we assess and benchmark the performance of such a network linking distant locations in Europe in terms of quantum key distribution rates, considering realistic parameters for currently available or near-term technology. Our results highlight the key parameters and the limits of current satellite quantum communication links and can be used to assist the design of future missions. We also discuss the possibility of using high-altitude balloons as an alternative to satellites

A high-throughput technique for determining grain boundary character non-destructively in microstructures with through-thickness grains

Grain boundaries (GBs) govern many properties of polycrystalline materials. However, because of their structural variability, our knowledge of GB constitutive relations is still very limited. We present a novel method to characterise the complete crystallography of individual GBs non-destructively, with high-throughput, and using commercially available tools. This method combines electron diffraction, optical reflectance and numerical image analysis to determine all five crystallographic parameters of numerous GBs in samples with through-thickness grains. We demonstrate the technique by measuring the crystallographic character of about 1,000 individual GBs in aluminum in a single run. Our method enables cost- and time-effective assembly of crystallography–property databases for thousands of individual GBs. Such databases are essential for identifying GB constitutive relations and for predicting GB-related behaviours of polycrystalline solids.United States. Department of Energy. Office of Basic Energy Sciences (award no DE-SC0008926)MIT International Science and Technology InitiativesNational Science Foundation (U.S.) (grant DMR-1003901

Identification of a novel pathway in sporadic Amyotrophic Lateral Sclerosis mediated by the long non-coding RNA ZEB1-AS1

Background: Deregulation of transcription in the pathogenesis of sporadic Amyotrophic Lateral Sclerosis (sALS) is taking central stage with RNA-sequencing analyses from sALS patients tissues highlighting numerous deregulated long non-coding RNAs (lncRNAs). The oncogenic lncRNA ZEB1-AS1 is strongly downregulated in peripheral blood mononuclear cells of sALS patients. In addition, in cancer-derived cell lines, ZEB1-AS1 belongs to a negative feedback loop regulation with hsa-miR-200c, acting as a molecular sponge for this miRNA. The role of the lncRNA ZEB1-AS1 in sALS pathogenesis has not been characterized yet, and its study could help identifying a possible disease-modifying target. Methods: the implication of the ZEB1-AS1/ZEB1/hsa-miR-200c/BMI1 pathway was investigated in multiple patients-derived cellular models (patients-derived peripheral blood mononuclear cells and induced pluripotent stem cells-derived neural stem cells) and in the neuroblastoma cell line SH-SY5Y, where its function was inhibited via RNA interference. Molecular techniques such as Real Time PCR, Western Blot and Immunofluorescence were used to assess the pathway dysregulation. Results: Our results show a dysregulation of a signaling pathway involving ZEB1-AS1/hsa-miR-200c/β-Catenin in peripheral blood mononuclear cells and in induced pluripotent stem cells-derived neural stem cells from sALS patients. These results were validated in vitro on the cell line SH-SY5Y with silenced expression of ZEB1-AS1. Moreover, we found an increase for ZEB1-AS1 during neural differentiation with an aberrant expression of β-Catenin, highlighting also its aggregation and possible impact on neurite length. Conclusions: Our results support and describe the role of ZEB1-AS1 pathway in sALS and specifically in neuronal differentiation, suggesting that an impairment of β-Catenin signaling and an alteration of the neuronal phenotype are taking place

COVID-19 in patients with Myasthenia Gravis: epidemiology and disease course

COVID-19, a disease caused by SARS-CoV-2 infection, has become a global pandemic. Patients with myasthenia gravis (MG), often treated with immunosuppressants, might be at higher risk of developing COVID-19 and of demonstrating a severe disease course. We aimed to study prevalence and describe features of COVID-19 in MG patients

Spatial modulation of visual responses arises in cortex with active navigation

During navigation, the visual responses of neurons in mouse primary visual cortex (V1) are modulated by the animal’s spatial position. Here we show that this spatial modulation is similarly present across multiple higher visual areas but negligible in the main thalamic pathway into V1. Similar to hippocampus, spatial modulation in visual cortex strengthens with experience and with active behavior. Active navigation in a familiar environment, therefore, enhances the spatial modulation of visual signals starting in the cortex

siRNA screen identifies QPCT as a druggable target for Huntington's disease.

Huntington's disease (HD) is a currently incurable neurodegenerative condition caused by an abnormally expanded polyglutamine tract in huntingtin (HTT). We identified new modifiers of mutant HTT toxicity by performing a large-scale 'druggable genome' siRNA screen in human cultured cells, followed by hit validation in Drosophila. We focused on glutaminyl cyclase (QPCT), which had one of the strongest effects on mutant HTT-induced toxicity and aggregation in the cell-based siRNA screen and also rescued these phenotypes in Drosophila. We found that QPCT inhibition induced the levels of the molecular chaperone αB-crystallin and reduced the aggregation of diverse proteins. We generated new QPCT inhibitors using in silico methods followed by in vitro screening, which rescued the HD-related phenotypes in cell, Drosophila and zebrafish HD models. Our data reveal a new HD druggable target affecting mutant HTT aggregation and provide proof of principle for a discovery pipeline from druggable genome screen to drug development

Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples

Funder: NCI U24CA211006Abstract: The Cancer Genome Atlas (TCGA) and International Cancer Genome Consortium (ICGC) curated consensus somatic mutation calls using whole exome sequencing (WES) and whole genome sequencing (WGS), respectively. Here, as part of the ICGC/TCGA Pan-Cancer Analysis of Whole Genomes (PCAWG) Consortium, which aggregated whole genome sequencing data from 2,658 cancers across 38 tumour types, we compare WES and WGS side-by-side from 746 TCGA samples, finding that ~80% of mutations overlap in covered exonic regions. We estimate that low variant allele fraction (VAF < 15%) and clonal heterogeneity contribute up to 68% of private WGS mutations and 71% of private WES mutations. We observe that ~30% of private WGS mutations trace to mutations identified by a single variant caller in WES consensus efforts. WGS captures both ~50% more variation in exonic regions and un-observed mutations in loci with variable GC-content. Together, our analysis highlights technological divergences between two reproducible somatic variant detection efforts