169 research outputs found

    Conceptual delimitations regarding the terminology used in the methods of investigating the future paper title

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    The authors propose the conceptual delimitation regarding the terminology used in the methods of investigating the future on the basis of a set of 7 variables. To this end, the hierarchical clusters? method will be used. The outcome of the research will be presented under the form of some clusters of terms with homogeneous meanings, almost synonyms, that would constitute the conceptual delimitation of the termsconceptual delimitation, anticipated future, cluster method

    Romanian Tritium for Nuclear Fusion

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    The demand for tritium is expected to increase when ITER (the International Thermonuclear Experimental Reactor) begins operation in the mid-2020s. Romania is expected to detritiate its CANDU (Canada Deuterium Uranium) units at Cernavoda starting 2024, with the goal of improving radiological safety and reactor performance. Detritiation will result in a significant quantity of tritium being produced and thus Romania has an opportunity to supply tritium for fusion. In this assessment, ITER has been used as a reference device requiring tritium, as the projected tritium extraction schedule from Cernavoda aligns favourably with ITER operation. The findings suggest that Romania is capable of providing a total of 6.2 kg of tritium to ITER over its 20 year operation, generating a potential revenue of 186M(USD).OpportunitiesassociatedwiththesupplyofRomanianhelium3arealsoconsideredasahedgingoption,whichhasthepotentialtogenerate186 M (USD). Opportunities associated with the supply of Romanian helium-3 are also considered as a hedging option, which has the potential to generate 120 M (USD) in the case of zero tritium sales. Greater involvement in future fission-fusion tritium-related activities through experience in tritium technologies is also discussed as a unique opportunity for Romania

    Pathway-Driven Rare Germline Variants Associated With Transplant-Associated Thrombotic Microangiopathy (TA-TMA)

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    The significance of rare germline mutations in transplant-associated thrombotic microangiopathy (TA-TMA) is not well studied. We performed a genetic association study in 100 adult TA-TMA patients vs. 98 post-transplant controls after matching by race, sex, and year. We focused on 5 pathways in complement, von Willebrand factor (VWF) function and related proteins, VWF clearance, ADAMTS13 function and related proteins, and endothelial activation (3641variants in 52 genes). In the primary analysis focused on 189 functional rare variants, no differential variant enrichment was observed in any of the pathways; specifically, 29 % TA-TMA and 33 % controls had at least 1 rare complement mutation. In the secondary analysis focused on 37 rare variants predicted to be pathogenic or likely pathogenic by ClinVar, Complement Database, or REVEL in-silico prediction tool, rare variants in the VWF clearance pathway were found to be significantly associated with TA-TMA (p = 0.008). On the gene level, LRP1 was the only one with significantly increased variants in TA-TMA in both analyses (p = 0.025 and 0.015). In conclusion, we did not find a significant association between rare variants in the complement pathway and TA-TMA; however, we discovered a new signal in the VWF clearance pathway driven by the gene LRP1 among likely pathogenic variants

    Exploring the impact of group identity at university on psychological and behavioural outcomes

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    With respect to supporting student well-being and success, the current research developed a peer support scheme, built on the principles of Social Identity Theory (SIT). This was targeted towards first year undergraduate psychology students, in which measures of collective identity, sense of belonging, group efficacy, happiness and resilience were obtained, along with attendance and academic attainment. Following one academic year of being part of our peer support scheme, participants (N= 90) completed a questionnaire and consented to their attendance and attainment data to be used. It was found that students’ collective identity was positively related to their sense of belonging, group efficacy beliefs and happiness. Further, the sense of belonging was a reliable predictor of happiness, but not attendance or academic attainment. Therefore, there is some evidence to suggest that a SIT-driven peer support scheme can support students’ psychosocial well-being, although more is needed to ascertain whether this could be developed further to observe any course-related outcomes. Theoretical contributions to SIT are therefore presented, in which the insights can be applied to Higher Education beyond the UK

    Rare deleterious germline variants and risk of lung cancer

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    Recent studies suggest that rare variants exhibit stronger effect sizes and might play a crucial role in the etiology of lung cancers (LC). Whole exome plus targeted sequencing of germline DNA was performed on 1045 LC cases and 885 controls in the discovery set. To unveil the inherited causal variants, we focused on rare and predicted deleterious variants and small indels enriched in cases or controls. Promising candidates were further validated in a series of 26,803 LCs and 555,107 controls. During discovery, we identified 25 rare deleterious variants associated with LC susceptibility, including 13 reported in ClinVar. Of the five validated candidates, we discovered two pathogenic variants in known LC susceptibility loci, ATM p.V2716A (Odds Ratio [OR] 19.55, 95%CI 5.04–75.6) and MPZL2 p.I24M frameshift deletion (OR 3.88, 95%CI 1.71–8.8); and three in novel LC susceptibility genes, POMC c.*28delT at 3′ UTR (OR 4.33, 95%CI 2.03–9.24), STAU2 p.N364M frameshift deletion (OR 4.48, 95%CI 1.73–11.55), and MLNR p.Q334V frameshift deletion (OR 2.69, 95%CI 1.33–5.43). The potential cancer-promoting role of selected candidate genes and variants was further supported by endogenous DNA damage assays. Our analyses led to the identification of new rare deleterious variants with LC susceptibility. However, in-depth mechanistic studies are still needed to evaluate the pathogenic effects of these specific alleles
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