94 research outputs found

    Fretting wear behaviour of MoS2 dry film lubricant

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    Dry film lubricants (DFL) are used as palliative coatings to prevent fretting wear. In this work fretting tests are carried out on coated Ti6Al4V cylinders on coated flat samples under dry sliding conditions, using an amplitude of 300 µm, 2.5 Hz frequency and 575 N normal loads. During the tests the coefficient of friction (CoF) was monitored, with tests being terminated when the coefficient of friction reached 0.7. Wear scars were analysed by profilometry and SEM to elucidate wear mechanisms. Results show that CoF initially increases rapidly to 0.4, this is then followed by a plateau region that finishes in a sudden step decrease in CoF following which CoF rises steadily. This behaviour is shown to be characteristic and interrupted tests are presented to allow elucidation of the wear scar at different stages in the lifetime and thus aid an understanding of the mechanisms of degradation which control the tribological behaviour

    Grasses as Biofactories: Scoping out the Opportunities

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    Key points 1. Plant biopharming is set to dominate commercial recombinant protein expression for specific proteins. 2. The choice of plant species depends on a multitude of factors and is determined on a caseby- case basis. 3. As a leaf based expression system grasses would have to compete predominantly with tobacco and alfalfa. 4. The grass-endophyte symbiosis offers a number of unique possibilities for biopharming

    Mechanical properties and microstructure of VPS and HVOF CoNiCrAlY coatings

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    HVOF and VPS coatings were sprayed using a Praxair (CO-210-24) CoNiCrAlY powder. Free standing coatings underwent vacuum annealing at different temperatures for times of up to 840h. Feedstock powder, as-sprayed and annealed coatings were characterised by SEM, EDS and XRD. The hardness and Young’s modulus of as-sprayed and annealed HVOF and VPS coatings were measured, including determination of Young’s moduli of the individual phases via nanoindentation and measurement of Young’s moduli of coatings at temperatures up to 500°C. The Eshelby inclusion model was used to investigate the effect of microstructure on the coatings’ mechanical properties. The sensitivity of the mechanical properties to microstructural details was confirmed. Young’s modulus was constant to ~200°C then decreased with increasing measurement temperature. Annealing increased Young’s modulus due to a combination of decreased porosity and β volume fraction. Oxide stringers in the HVOF coating maintained its higher hardness than the VPS coating even after annealing

    The Impact of Entrepreneurship Education in Higher Education: A Systematic Review and Research Agenda

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    Using a teaching model framework, we systematically review empirical evidence on the impact of entrepreneurship education (EE) in higher education on a range of entrepreneurial outcomes, analyzing 159 published articles from 2004 to 2016. The teaching model framework allows us for the first time to start rigorously examining relationships between pedagogical methods and specific outcomes. Reconfirming past reviews and meta-analyses, we find that EE impact research still predominantly focuses on short-term and subjective outcome measures and tends to severely underdescribe the actual pedagogies being tested. Moreover, we use our review to provide an up-to-date and empirically rooted call for less obvious, yet greatly promising, new or underemphasized directions for future research on the impact of university-based entrepreneurship education. This includes, for example, the use of novel impact indicators related to emotion and mind-set, focus on the impact indicators related to the intention-to-behavior transition, and exploring the reasons for some contradictory findings in impact studies including person-, context-, and pedagogical model-specific moderator

    Enhancing discovery of genetic variants for posttraumatic stress disorder through integration of quantitative phenotypes and trauma exposure information

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    Background Posttraumatic stress disorder (PTSD) is heritable and a potential consequence of exposure to traumatic stress. Evidence suggests that a quantitative approach to PTSD phenotype measurement and incorporation of lifetime trauma exposure (LTE) information could enhance the discovery power of PTSD genome-wide association studies (GWASs). Methods A GWAS on PTSD symptoms was performed in 51 cohorts followed by a fixed-effects meta-analysis (N = 182,199 European ancestry participants). A GWAS of LTE burden was performed in the UK Biobank cohort (N = 132,988). Genetic correlations were evaluated with linkage disequilibrium score regression. Multivariate analysis was performed using Multi-Trait Analysis of GWAS. Functional mapping and annotation of leading loci was performed with FUMA. Replication was evaluated using the Million Veteran Program GWAS of PTSD total symptoms. Results GWASs of PTSD symptoms and LTE burden identified 5 and 6 independent genome-wide significant loci, respectively. There was a 72% genetic correlation between PTSD and LTE. PTSD and LTE showed largely similar patterns of genetic correlation with other traits, albeit with some distinctions. Adjusting PTSD for LTE reduced PTSD heritability by 31%. Multivariate analysis of PTSD and LTE increased the effective sample size of the PTSD GWAS by 20% and identified 4 additional loci. Four of these 9 PTSD loci were independently replicated in the Million Veteran Program. Conclusions Through using a quantitative trait measure of PTSD, we identified novel risk loci not previously identified using prior case-control analyses. PTSD and LTE have a high genetic overlap that can be leveraged to increase discovery power through multivariate methods

    International meta-analysis of PTSD genome-wide association studies identifies sex- and ancestry-specific genetic risk loci

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    The risk of posttraumatic stress disorder (PTSD) following trauma is heritable, but robust common variants have yet to be identified. In a multi-ethnic cohort including over 30,000 PTSD cases and 170,000 controls we conduct a genome-wide association study of PTSD. We demonstrate SNP-based heritability estimates of 5–20%, varying by sex. Three genome-wide significant loci are identified, 2 in European and 1 in African-ancestry analyses. Analyses stratified by sex implicate 3 additional loci in men. Along with other novel genes and non-coding RNAs, a Parkinson’s disease gene involved in dopamine regulation, PARK2, is associated with PTSD. Finally, we demonstrate that polygenic risk for PTSD is significantly predictive of re-experiencing symptoms in the Million Veteran Program dataset, although specific loci did not replicate. These results demonstrate the role of genetic variation in the biology of risk for PTSD and highlight the necessity of conducting sex-stratified analyses and expanding GWAS beyond European ancestry populations. © 2019, This is a U.S. government work and not under copyright protection in the U.S.; foreign copyright protection may apply

    Dentin matrix protein 1 and phosphate homeostasis are critical for postnatal pulp, dentin and enamel formation

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    Deletion or mutation of dentin matrix protein 1 (DMP1) leads to hypophosphatemic rickets and defects within the dentin. However, it is largely unknown if this pathological change is a direct role of DMP1 or an indirect role of phosphate (Pi) or both. It has also been previously shown that Klotho-deficient mice, which displayed a high Pi level due to a failure of Pi excretion, causes mild defects in the dentinal structure. This study was to address the distinct roles of DMP1 and Pi homeostasis in cell differentiation, apoptosis and mineralization of dentin and enamel. Our working hypothesis was that a stable Pi homeostasis is critical for postnatal tooth formation, and that DMP1 has an antiapoptotic role in both amelogenesis and dentinogenesis. To test this hypothesis, Dmp1-null (Dmp1(−/−)), Klotho-deficient (kl/kl), Dmp1/Klotho-double-deficient (Dmp1(−/−)/kl/kl) and wild-type (WT) mice were killed at the age of 6 weeks. Combinations of X-ray, microcomputed tomography (μCT), scanning electron microscopy (SEM), histology, apoptosis and immunohistochemical methods were used for characterization of dentin, enamel and pulp structures in these mutant mice. Our results showed that Dmp1(−/−) (a low Pi level) or kl/kl (a high Pi level) mice displayed mild dentin defects such as thin dentin and a reduction of dentin tubules. Neither deficient mouse line exhibited any apparent changes in enamel or pulp structure. However, the double-deficient mice (a high Pi level) displayed severe defects in dentin and enamel structures, including loss of dentinal tubules and enamel prisms, as well as unexpected ectopic ossification within the pulp root canal. TUNEL assay showed a sharp increase in apoptotic cells in ameloblasts and odontoblasts. Based on the above findings, we conclude that DMP1 has a protective role for odontoblasts and ameloblasts in a pro-apoptotic environment (a high Pi level)
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