199 research outputs found

    Czechoslovak-Polish relations 1918-1968: The prospects for mutual support in the case of revolt

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    Mortality and immortality : the Nobel Prize as an experiment into the effect of status upon longevity

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    It has been known for centuries that the rich and famous have longer lives than the poor and ordinary. Causality, however, remains trenchantly debated. The ideal experiment would be one in which extra status could somehow be dropped upon a sub-sample of individuals while those in a control group of comparable individuals received none. This paper attempts to formulate a test in that spirit. It collects 19th-century birth data on science Nobel Prize winners. Correcting for potential biases, we estimate that winning the Prize, compared to merely being nominated, is associated with between 1 and 2 years of extra longevity

    Investigation of Rhine Pointing as a Solution to the Aircraft Human Machine Interface Problem

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    The human machine interface in 5th generation aircraft has not evolved proportionally with advances in display size and data density. The traditional cursor slew method fails to rapidly relocate the cursor, especially on large displays. Previous studies at the Air Force Test Pilot School and Air Force Institute of Technology identified methods that have the potential to improve the human machine interface. This research expanded upon those studies by providing an assessment of head tracking technology as a secondary method of cursor manipulation. Specifically, this study examined the effects that visual feedback (visible and invisible head tracking cursors) and cursor configurations (Z-Axis and X/Y-Axis snap button) had on performance in a target selection task. A Fitts Law regression was conducted to fit the collected data to a predictive model, but this was unsuccessful. Dependent variables such as time to initiate head tracking snap, accuracy of head tracking snap, and total time to select target were examined to compare the different configurations. After initial data analysis was complete, an assessment of learning effects was conducted. The initial data analysis found all head tracking configurations to be faster than the traditional cursor slew method. Visible conditions were consistently more accurate and had lower total selection times than the invisible conditions. Invisible conditions had faster times to initiate the cursor snap, indicating that the participants were not attempting to make fine adjustments with the head tracking cursor. There were no observed learning effects in this study. The resulting conclusions are discussed and recommendations for future research are proposed including study of fatigue in the target selection task, target selection as a secondary task, and the combination of rhino pointing with eye tracking capabilities

    Steric Shielding of Surface Epitopes and Impaired Immune Recognition Induced by the Ebola Virus Glycoprotein

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    Many viruses alter expression of proteins on the surface of infected cells including molecules important for immune recognition, such as the major histocompatibility complex (MHC) class I and II molecules. Virus-induced downregulation of surface proteins has been observed to occur by a variety of mechanisms including impaired transcription, blocks to synthesis, and increased turnover. Viral infection or transient expression of the Ebola virus (EBOV) glycoprotein (GP) was previously shown to result in loss of staining of various host cell surface proteins including MHC1 and β1 integrin; however, the mechanism responsible for this effect has not been delineated. In the present study we demonstrate that EBOV GP does not decrease surface levels of β1 integrin or MHC1, but rather impedes recognition by steric occlusion of these proteins on the cell surface. Furthermore, steric occlusion also occurs for epitopes on the EBOV glycoprotein itself. The occluded epitopes in host proteins and EBOV GP can be revealed by removal of the surface subunit of GP or by removal of surface N- and O- linked glycans, resulting in increased surface staining by flow cytometry. Importantly, expression of EBOV GP impairs CD8 T-cell recognition of MHC1 on antigen presenting cells. Glycan-mediated steric shielding of host cell surface proteins by EBOV GP represents a novel mechanism for a virus to affect host cell function, thereby escaping immune detection

    Improving Workplace Wellbeing: What Made a Difference?

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    Abstract Text: Purpose: To investigate previous efforts and to identify promising workplace strategies to improve professional wellbeing among nurses.Background: There is a mental health crisis in nursing that contributes to high rates of intention to leave (1,2). Systems-based approaches that go beyond the individual are crucial (2,3). But little is known about workplace-based approaches that can improve nurse mental health (1,2).Methods: We deductively and inductively analyzed 1317 nurses’ survey-based free-text descriptions of strategies used by their workplaces to improve professional wellbeing. Details about the Michigan Nurses Study have been published previously (4). We compared responses from nurses who plan to leave their position to responses from nurses who don’t.Results: The most common response was that the workplace had made no effort. Nurses who intended to leave reported no effort more often (40.8%) than nurses who didn’t (24.9%). The second most common response was increased compensation (e.g., bonuses, incentive pay); the third was improved facilities and other benefits (e.g., break rooms, free food and beverages). Self-scheduling and team huddles were also identified by multiple participants as helpful.Conclusions: Zero effort from workplaces may contribute to nurses’ intent to leave. Approaches that improve professional wellbeing include increased compensation and enhanced facilities. Further research into self-scheduling and daily huddles, which have previously shown promise in boosting staff satisfaction (5), may identify implementation practices best suited to enhancing nurse wellbeing

    Clinical grade manufacturing of human alloantigen-reactive regulatory T cells for use in transplantation.

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    Regulatory T cell (Treg) therapy has the potential to induce transplantation tolerance so that immunosuppression and associated morbidity can be minimized. Alloantigen-reactive Tregs (arTregs) are more effective at preventing graft rejection than polyclonally expanded Tregs (PolyTregs) in murine models. We have developed a manufacturing process to expand human arTregs in short-term cultures using good manufacturing practice-compliant reagents. This process uses CD40L-activated allogeneic B cells to selectively expand arTregs followed by polyclonal restimulation to increase yield. Tregs expanded 100- to 1600-fold were highly alloantigen reactive and expressed the phenotype of stable Tregs. The alloantigen-expanded Tregs had a diverse TCR repertoire. They were more potent than PolyTregs in vitro and more effective at controlling allograft injuries in vivo in a humanized mouse model
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