267 research outputs found

    USING GEOMATICS TO UNDERSTAND AND VALORIZE HERITAGE, THREE DIFFERENT CONTEXTS OF STUDY: SYRIA, ITALY, AND FRANCE

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    Such innovative meeting dedicated to Cultural Heritage: challenges, new perspectives, and technological innovation are ‘vital’ in order to exchange different experiences, needs, opportunities, and, above all, to find new approaches to preserve, at least, the memory of heritage for further generations. This paper includes some experiences accumulated throughout several topographic projects concerning Christianity during the Late Antiquity and Early Medieval Ages in northern Syria, in Liguria in Italy, and in Provence in France. Geospatial and Geomatics data have been used in these investigations, since 2007, thanks to the Pontifical Institute of Christian Archaeology of Rome, the National Institute for Art History in Paris, Nino Lamboglia Foundation, and Marc de Montalembert Foundation. The Geospatial data highlighted for the first time, after about a century of research, much un- published data about Syrian monasteries. One of our goals was to understand what the exact differences are from all points of view: time, results, and economic costs between Agisoft Photoscan and MicMac. The models of the two applications are well made, but we noticed that the model created by MicMac software is excellent, despite being an open source application. In 2017, due to the positive geomathic results during the last three seasons of our excavations on the site of Capo Don, the first Multimedial Exhibition Space (SEM) of the town Riva Ligure was inaugurated, thanks to Comune of Riva Ligure, and all research team members guided by professor Philippe Pergola. Geomatics is a powerful tool not only for preserving memories, but it is ideal for dissemination heritage on the public levels, exactly like the role of archaeology

    Congenital chloride diarrhea clinical features and management: a systematic review

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    Introduction: Congenital chloride diarrhea (CLD) is a rare autosomal recessive disorder characterized by watery diarrhea with a high level of fecal Cl−, metabolic alkalosis, and electrolyte alterations. Several intestinal and extraintestinal complications and even death can occur. An optimal knowledge of the clinical features and best therapeutic strategies is mandatory for an effective management. Methods: Articles published between 1 January 1965 and 31 December 2019, reported in PUBMED and EMBASE, were evaluated for a systematic review analyzing four categories: anamnestic features, clinical features, management, and follow-up strategies. Results: Fifty-seven papers reporting information on 193 CLD patients were included. The most common anamnestic features were positive family anamnesis for chronic diarrhea (44.4%), consanguinity (75%), polyhydramnios (98.3%), preterm delivery (78.6%), and failure to pass meconium (60.7%). Mean age at diarrhea onset was 6.63 days. Median diagnostic delay was 60 days. Prenatal diagnosis, based on molecular analysis, was described in 40/172 (23.3%). All patients received NaCl/KCl-substitutive therapy. An improvement of diarrhea during adulthood was reported in 91.3% of cases. Failure to thrive (21.6%) and chronic kidney disease (17.7%) were the most common complications. Conclusions: This analysis of a large population suggests the necessity of better strategies for the management of CLD. A close follow-up and a multidisciplinary approach is mandatory to manage this condition characterized by heterogeneous and multisystemic complications. Impact: In this systematic review, we describe data regarding anamnestic features, clinical features, management, and follow-up of CLD patients obtained from the largest population of patients ever described to date.The results of our investigation could provide useful insights for the diagnostic approach and the management of this condition

    Additive Manufacturing Technology for High Performances Feed Horn

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    In this work the design and manufacturing through selective laser melting technology of single-band dual circular feed-system operating in Ka-band is reported. In the feed design an AM oriented architecture has been employed. The measured performances confirms the good manufacturing of the system that satisfies very stringent requirements in terms of polarization purity

    Sensitivity of Non-Contrast Computed Tomography for Small Renal Calculi with Endoscopy as the Gold Standard

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    Objectives To compare the sensitivity of non-contrast CT to endoscopy for detection of renal calculi. Imaging modalities for detection of nephrolithiasis have centered on abdominal x-ray (KUB), ultrasound (US), and non-contrast computed tomography (CT). Sensitivities of 58-62% (KUB), 45% (US), and 95-100% (CT) have been previously reported. However, these results have never been correlated with endoscopic findings. Methods Idiopathic calcium oxalate stone formers with symptomatic calculi requiring ureteroscopy (URS) were studied. At the time of surgery, the number and location of all calculi within the kidney were recorded followed by basket retrieval. Each calculus was measured and sent for micro CT and infrared spectrophotometry. All CT scans were reviewed by the same genitourinary radiologist who was blinded to the endoscopic findings. The radiologist reported on the number, location, and size of each calculus. Results 18 renal units were studied in 11 patients. Average time from CT scan to URS was 28.6 days. The mean number of calculi identified per kidney was 9.2±6.1 for endoscopy and 5.9±4.1 for CT (p<0.004). The mean size of total renal calculi (sum of longest stone diameters) per kidney was 22.4±17.1 mm and 18.2±13.2 mm for endoscopy and CT, respectively (p=0.06). Conclusions CT scan underreports the number of renal calculi, probably missing some small stones and unable to distinguish those lying in close proximity to one another. However, the total stone burden seen by CT is, on average, accurate when compared to that found on endoscopic examination

    Spiro-containing derivatives show antiparasitic activity against trypanosoma brucei through inhibition of the trypanothione reductase enzyme

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    Trypanothione reductase (TR) is a key enzyme that catalyzes the reduction of trypa-nothione, an antioxidant dithiol that protects Trypanosomatid parasites from oxidative stress induced by mammalian host defense systems. TR is considered an attractive target for the development of novel anti-parasitic agents as it is essential for parasite survival but has no close homologue in humans. We report here the identification of spiro-containing derivatives as inhibitors of TR from Trypanosoma brucei (TbTR), the parasite responsible for Human African Trypanosomiasis. The hit series, identified by high throughput screening, was shown to bind TbTR reversibly and to compete with the trypanothione (TS2) substrate. The prototype compound 1 from this series was also found to impede the growth of Trypano-soma brucei parasites in vitro. The X-ray crystal structure of TbTR in complex with compound 1 solved at 1.98 Å allowed the identification of the hydrophobic pocket where the inhibitor binds, placed close to the catalytic histidine (His 461’) and lined by Trp21, Val53, Ile106, Tyr110 and Met113. This new inhibitor is specific for TbTR and no activity was detected against the structurally similar human glutathione reductase (hGR). The central spiro scaffold is known to be suitable for brain active compounds in humans thus represent-ing an attractive starting point for the future treatment of the central nervous system stage of T. brucei infections

    UAV-Based Antenna Measurements: Improvement of the Test Source Frequency Behavior

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    Drone-based radiation pattern measurements require the knowledge of the whole test-source radiation pattern in order to reach the expected measurement accuracy. However, the radiation pattern of the onboard antenna can be highly distorted by the metal frame of the vehicle, particularly in the VHF and UHF bands, showing highly resonant behaviors. This paper presents a preliminary analysis aimed to highlight such behavior and adopt compatible solutions to minimize or avoid the pattern distortion in the frequency of interest

    First Results on the Experimental Validation of the SKA-low Prototypes Deployed in Australia Using an Airborne Test Source

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    As the Square Kilometre Array progresses toward the construction phase, the first prototypes of the low-frequency instrument have been deployed in Australia. To support such a crucial phase, a measurement campaign took place in the Murchison Radio-astronomy Observatory area in order to validate the electromagnetic models of the arrays by characterizing the embedded-element patterns and the array beams. A set of significant results is shown in this contribution

    Mechanism of Chemical Activation of Nrf2

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    NF-E2 related factor-2 (Nrf2) promotes the transcription of many cytoprotective genes and is a major drug target for prevention of cancer and other diseases. Indeed, the cancer-preventive activities of several well-known chemical agents were shown to depend on Nrf2 activation. It is well known that chemopreventive Nrf2 activators stabilize Nrf2 by blocking its ubiquitination, but previous studies have indicated that this process occurs exclusively in the cytoplasm. Kelch-like ECH-associated protein 1 (Keap1) binds to Nrf2 and orchestrates Nrf2 ubiquitination, and it has been a widely-held view that inhibition of Nrf2 ubiquitination by chemopreventive agents results from the dissociation of Nrf2 from its repressor Keap1. Here, we show that while the activation of Nrf2 by prototypical chemical activators, including 5,6-dihydrocyclopenta-1,2-dithiole-3-thione (CPDT) and sulforaphane (SF), results solely from inhibition of its ubiquitination, such inhibition occurs predominantly in the nucleus. Moreover, the Nrf2 activators promote Nrf2 association with Keap1, rather than disassociation, which appears to result from inhibition of Nrf2 phosphorylation at Ser40. Available evidence suggests the Nrf2 activators may block Nrf2 ubiquitination by altering Keap1 conformation via reaction with the thiols of specific Keap1 cysteines. We further show that while the inhibitory effects of CPDT and SF on Nrf2 ubiquitination depend entirely on Keap1, Nrf2 is also degraded by a Keap1-independent mechanism. These findings provide significant new insight about Nrf2 activation and suggest that exogenous chemical activators of Nrf2 enter the nucleus to exert most of their inhibitory impact on Nrf2 ubiquitination and degradation
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