4,731 research outputs found

    Undergraduate Research: The Jetmore Food Center

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    The Jetmore Food Center aids the community by providing food to the citizens of Jetmore. In general, the majority of those that shop in the Jetmore Food Center are above the age of 40, but the store serves to customers of all ages. The store opens at 8 A.M and stays open until 8 P.M at night six days a week. In the past, stores in Jetmore closed at 6 P.M every day and closed on Sundays. This caused problems for many residents of Jetmore, as many work in Dodge City and did not return to Jetmore until the evening. Like most small town’s grocery stores, the Jetmore Food Center donates food and drinks to the school, the hospital, as well as clubs and organizations that hold special events in Jetmore. Once again, aiding and partaking in events in the community further strengthens townspeople’s confidence in their local grocer, which in turn helps a store succeed. Also, unlike chain stores, the profit dollars made from a small-town grocery store circulate back into the community. Without a doubt, the Jetmore Food Center keeps Jetmore a successful small town in Kansas. From offering quality food at reasonable prices, to providing jobs for the youth and teaching them vital skills for adulthood, the Jetmore Food Center is the lifeblood of the community of Jetmore

    Fully Collapsed Imploded Cryptophanes in Solution and in the Solid State

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    Cryptophanes with flexible linkers derived from (±)‐tris‐(4‐formyl‐phenyl)‐cyclotriguaiacylene with either bisoxydi(ethylamine) or bis(aminopropyl)ether were isolated as single crystals, the crystal structures of which showed the proposed, but previously uncharacterised, out‐in conformation, in which both cyclotriguaiacylene fragments adopt a crown conformation with one crown sitting inside the other. The usual cage‐like out‐out conformation of the cryptophanes was observed when crystals were dissolved upon heating, and the molecules collapsed back to the out‐in isomers over time. In contrast, a cryptophane also derived from (±)‐tris‐(4‐formyl‐phenyl)‐cyclotriguaiacylene but with rigid dibenzalhydrazine linkers was isolated as the more usual out‐out isomer

    Glycine zinc sulfate penta-hydrate: redetermination at 10 K from time-of-flight neutron Laue diffraction

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    Single crystals of glycine zinc sulfate penta-hydrate [systematic name: hexa-aqua-zinc tetra-aquadiglycinezinc bis-(sulfate)], [Zn(H2O)6][Zn(C2H5NO2)2(H2O)4](SO4)2, have been grown by isothermal evaporation from aqueous solution at room temperature and characterized by single-crystal neutron diffraction. The unit cell contains two unique ZnO6 octa-hedra on sites of symmetry -1 and two SO4 tetra-hedra with site symmetry 1; the octa-hedra comprise one [tetra-aqua-diglycine zinc](2+) ion (centred on one Zn atom) and one [hexa-aqua-zinc](2+) ion (centred on the other Zn atom); the glycine zwitterion, NH3(+)CH2COO(-), adopts a monodentate coordination to the first Zn atom. All other atoms sit on general positions of site symmetry 1. Glycine forms centrosymmetric closed cyclic dimers due to N-H⋯O hydrogen bonds between the amine and carboxyl-ate groups of adjacent zwitterions and exhibits torsion angles varying from ideal planarity by no more than 1.2°, the smallest values for any known glycine zwitterion not otherwise constrained by a mirror plane. This work confirms the H-atom locations estimated in three earlier single-crystal X-ray diffraction studies with the addition of independently refined fractional coordinates and Uij parameters, which provide accurate inter-nuclear X-H (X = N, O) bond lengths and consequently a more accurate and precise depiction of the hydrogen-bond framework

    Discrepancies in autologous bone marrow stem cell trials and enhancement of ejection fraction (DAMASCENE): weighted regression and meta-analysis

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    Objective To investigate whether discrepancies in trials of use of bone marrow stem cells in patients with heart disease account for the variation in reported effect size in improvement of left ventricular function. Design Identification and counting of factual discrepancies in trial reports, and sample size weighted regression against therapeutic effect size. Meta-analysis of trials that provided sufficient information. Data sources PubMed and Embase from inception to April 2013. Eligibility for selecting studies Randomised controlled trials evaluating the effect of autologous bone marrow stem cells for heart disease on mean left ventricular ejection fraction. Results There were over 600 discrepancies in 133 reports from 49 trials. There was a significant association between the number of discrepancies and the reported increment in EF with bone marrow stem cell therapy (Spearman’s r=0.4, P=0.005). Trials with no discrepancies were a small minority (five trials) and showed a mean EF effect size of −0.4%. The 24 trials with 1-10 discrepancies showed a mean effect size of 2.1%. The 12 with 11-20 discrepancies showed a mean effect of size 3.0%. The three with 21-30 discrepancies showed a mean effect size of 5.7%. The high discrepancy group, comprising five trials with over 30 discrepancies each, showed a mean effect size of 7.7%. Conclusions Avoiding discrepancies is difficult but is important because discrepancy count is related to effect size. The mechanism is unknown but should be explored in the design of future trials because in the five trials without discrepancies the effect of bone marrow stem cell therapy on ejection fraction is zero

    Embroidered Electromyography: A Systematic Design Guide

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    Designing Embroidered Electrodes for Wearable Surface Electromyography

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    This work was supported by the UK Crafts Council as part of the Parallel Practices project, by the Seventh Framework Programme of the European Commission under grant agreement 287728 in the framework of EU project STIFF-FLOP and by the Horizon 2020 Research and Innovation Programme under grant agreement 637095 in the framework of EU project FourByThree

    Self-Assembly and Host–Guest Interactions of Pd3L2 Metallo-cryptophanes with Photoisomerizable Ligands

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    New photoswitchable pyridyl-azo-phenyl-decorated tripodal host ligands (Laz) that belong to the cyclotriveratrylene family have been synthesized, and their photoswitching behavior and crystal structures determined. The latter includes a remarkable 7-fold Borromean-weave entanglement of π–π stacked layers. Trigonal bipyramidal {[Pd(en)]3(Laz)2}6+ metallo-cryptophanes (en = ethylenediamine) were formed from these and a previously known pyridyl-azo-phenyl-decorated tripodal host ligand. These coordination cages dissociate at low concentrations and are less robust to photoswitching of the Laz ligands than were previously reported Ir(III)-linked metallo-cryptophanes with similar ligands, reflecting the greater lability of the Pd–N bonds. The {[Pd(en)]3(Laz)2}6+ cages all act as hosts, binding octyl sulfate anions, or N-[2-(dimethylamino)ethyl]-1,8-naphthalimide in a dimethyl sulfoxide solution

    Acute hot water immersion is protective against impaired vascular function following forearm ischemia-reperfusion in young healthy humans.

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    Ischemia-reperfusion (I/R) injury is a primary cause of poor outcomes following ischemic cardiovascular events. We tested whether acute hot water immersion protects against forearm vascular I/R. METHODS: Ten (5 male, 5 female) young (23±2 years), healthy subjects participated in two trials in random order 7-21 days apart, involving: 1) 60-min of seated rest (control), or 2) 60-min of immersion in 40.5°C water (peak rectal temperature: 38.9±0.2°C). I/R was achieved 70 min following each intervention by inflating an upper arm cuff to 250mmHg for 20-min followed by 20-min of reperfusion. Brachial artery flow-mediated dilation (FMD) and forearm post-occlusive reactive hyperemia (RH) were measured as markers of macro- and micro-vascular function at three time points: 1) pre-intervention, 2) 60-min post-intervention, and 3) post-I/R. RESULTS: Neither time control nor hot water immersion alone affected FMD (both p>0.99). I/R reduced FMD from 7.4±0.7 to 5.4±0.6% (p=0.03) and this reduction was prevented following hot water immersion (7.0±0.7 to 7.7±1.0%; p>0.99). I/R also impaired RH (peak vascular conductance: 2.6±0.5 to 2.0±4mL∙min(-1)∙mmHg(-1), p=0.003), resulting in a reduced shear stimulus (SRAUC/10(-3) : 22.5±2.4 to 16.9±2.4, p=0.04). The post-I/R reduction in peak RH was prevented by hot water immersion (2.5±0.4 to 2.3±0.4mL∙min(-1)∙mmHg(-1); p=0.33). CONCLUSIONS: We observed a decline in brachial artery dilator function post-I/R, which may be (partly) related to damage incurred downstream in the microvasculature, as indicated by impaired RH and shear stimulus. Hot water immersion was protective against reductions in FMD and RH post-I/R, suggesting heat stress induces vascular changes consistent with reducing I/R injury following ischemic events

    Direct observation of delithiation as the origin of analog memristance in LixNbO2

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    The discovery of analog LixNbO2 memristors revealed a promising new memristive mechanism wherein the diffusion of Li+ rather than O2- ions enables precise control of the resistive states. However, directly correlating lithium concentration with changes to the electronic structure in active layers remains a challenge and is required to truly understand the underlying physics. Chemically delithiated single crystals of LiNbO2 present a model system for correlating lithium variation with spectroscopic signatures from operando soft x-ray spectroscopy studies of device active layers. Using electronic structure modeling of the x-ray spectroscopy of LixNbO2 single crystals, we demonstrate that the intrinsic memristive behavior in LixNbO2 active layers results from field-induced degenerate p-type doping. We show that electrical operation of LixNbO2-based memristors is viable even at marginal Li deficiency and that the analog memristive switching occurs well before the system is fully metallic. This study serves as a benchmark for material synthesis and characterization of future LixNbO2-based memristor devices and suggests that valence change switching is a scalable alternative that circumvents the electroforming typically required for filamentary-based memristors
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