303 research outputs found

    Comparative analysis and optimization of technical and weight parameters of turbo-electric propulsion systems

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    According to Flightpath 2050, the aviation industry is aiming to substantially reduce emissions over the coming decades. One possible solution to meet these ambitious goals is by moving to hybrid-electric drivetrain architectures which require the electric components to be extremely lightweight and efficient at the same time. It has been claimed in several publications that cryogenic and in particular superconducting components can help to fulfill such requirements that potentially cannot be achieved with non-cryogenic components. The purpose of this work was to make a fair comparison between a cryogenic turbo-electric propulsion system (CEPS) and a non-cryogenic turbo-electric propulsion system (TEPS) on a quantitative level. The results on the CEPS were presented in detail in a previous publication. The focus of this publication is to present the study on the TEPS, which in conclusion allows a direct comparison. For both systems the same top-level aircraft requirements were used that were derived within the project TELOS based on an exemplary mission profile and the physical measures of a 220-passenger aircraft. Our study concludes that a CEPS could be 10% to 40% lighter than a TEPS. Furthermore, a CEPS could have a total efficiency gain of up to 18% compared to a similar TEPS

    Genotoxic agents promote the nuclear accumulation of annexin A2: role of annexin A2 in mitigating DNA damage

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    Annexin A2 is an abundant cellular protein that is mainly localized in the cytoplasm and plasma membrane, however a small population has been found in the nucleus, suggesting a nuclear function for the protein. Annexin A2 possesses a nuclear export sequence (NES) and inhibition of the NES is sufficient to cause nuclear accumulation. Here we show that annexin A2 accumulates in the nucleus in response to genotoxic agents including gamma-radiation, UV radiation, etoposide and chromium VI and that this event is mediated by the nuclear export sequence of annexin A2. Nuclear accumulation of annexin A2 is blocked by the antioxidant agent N-acetyl cysteine (NAC) and stimulated by hydrogen peroxide (H2O2), suggesting that this is a reactive oxygen species dependent event. In response to genotoxic agents, cells depleted of annexin A2 show enhanced phospho-histone H2AX and p53 levels, increased numbers of p53-binding protein 1 nuclear foci and increased levels of nuclear 8-oxo-2'-deoxyguanine, suggesting that annexin A2 plays a role in protecting DNA from damage. This is the first report showing the nuclear translocation of annexin A2 in response to genotoxic agents and its role in mitigating DNA damage.Natural Sciences and Engineering Research Council of Canada (NSERC); European Union [PCOFUND-GA-2009-246542]; Foundation for Science and Technology of Portugal; Beatrice Hunter Cancer Research Institute; Terry Fox Foundationinfo:eu-repo/semantics/publishedVersio

    2,4-Dinitro-1-naphthol

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    In the title compound, C10H6N2O5, the two fused rings are almost co-planar, with an r.m.s. deviation of 0.0163 Å. The nitro groups are oriented at dihedral angles of 2.62 (11) and 44.69 (11)° with respect to the plane of the parent fused rings. Intra­molecular O—H⋯O and C—H⋯O hydrogen bonds complete S(6) ring motifs. In the crystal, mol­ecules are linked into chains along [101] by inter­molecular O—H⋯O hydrogen bonds. π–π inter­actions [centroid–centroid distances = 3.6296 (15), 3.8104 (15) and 3.6513 (14) Å] might play a role in stabilizing the structure

    Replication of KCNJ11 (p.E23K) and ABCC8 (p.S1369A) association in Russian diabetes mellitus 2 type cohort and meta-analysis

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    © 2015 Sokolova et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. The genes ABCC8 and KCNJ11 have received intense focus in type 2 diabetes mellitus (T2DM) research over the past two decades. It has been hypothesized that the p.E23K (KCNJ11) mutation in the 11p15.1 region may play an important role in the development of T2DM. In 2009, Hamming et al. found that the p.1369A (ABCC8) variant may be a causal factor in the disease; therefore, in this study we performed a meta-analysis to evaluate the association between these single nucleotide polymorphisms (SNPs), including our original data on the Siberian population (1384 T2DM and 414 controls). We found rs5219 and rs757110 were not associated with T2DM in this population, and that there was linkage disequilibrium in Siberians (D'=0.766, r2= 0.5633). In addition, the haplotype rs757110[T]- rs5219[C] (p.23K/p.S1369) was associated with T2DM (OR = 1.52, 95% CI: 1.04-2.24). We included 44 original studies published by June 2014 in a meta-analysis of the p.E23K association with T2DM. The total OR was 1.14 (95% CI: 1.11-1.17) for p.E23K for a total sample size of 137,298. For p.S1369A, a meta-analysis was conducted on a total of 10 studies with a total sample size of 14,136 and pooled OR of 1.14 [95% CI (1.08-1.19); p = 2 × 10-6]. Our calculations identified causal genetic variation within the ABCC8/KCNJ11region for T2DM with an OR of approximately 1.15 in Caucasians and Asians. Moreover, the OR value was not dependent on the frequency of p.E23K or p.S1369A in the populations

    Reconstruction of bone segment of the glenoid at chronic recurrent anterior shoulder instability using porous titanium nickelide

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    A method of the surgical treatment of posttraumatic recurrent shoulder instability with bony defects using porous NiTiis presented. We operated 5 patients using this method. Recurrences of dislocation after surgical treatment have not been recorded. The method is an alternative to Latarjet procedure and iliac crest bone grafting. We use computerized tomography data in the preoperative making of NiTi graft. The graft is sawed from billet having a cylindrical shape about 1 cm thick. Than by using the drill we form two screw holes. A prepared graft is subsequently installed in the area of the glenoid bone defect. The advantages of this method are accurate reconstruction of the bony defect, minimal risk of recurrences, absence of resorption, reduction of procedure time
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