2,488 research outputs found

    Selected results on Strong and Coulomb-induced correlations from the STAR experiment

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    Using recent high-statistics STAR data from Au+Au and Cu+Cu collisions at full RHIC energy I discuss strong and Coulomb-induced final state interaction effects on identical (ππ\pi-\pi) and non-identical (πΞ\pi-\Xi) particle correlations. Analysis of πΞ\pi-\Xi correlations reveals the strong and Coulomb-induced FSI effects allowing for the first time to estimate space extension of π\pi and Ξ\Xi sources and average shift between them. Source imaging technique providing clean separation of these effects from effects due to the source function itself is applied to one-dimensional relative momentum correlation function of identical pions. For low momentum pions and/or non-central collisions large departure from a single-Gaussian shape is observed

    Nickel versus palladium in cross-coupling catalysis : on the role of substrate coordination to zerovalent metal complexes

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    We report a detailed comparison of the effect of coordinating functional groups on the performance of Suzuki-Miyaura reactions catalysed by nickel and palladium, using competition experiments, robustness screening, and density functional theory calculations. Nickel can interact with a variety of functional groups, which manifests as selectivity in competitive cross-coupling reactions. The presence of these functional groups on exogenous additives has a range of effects on cross-coupling reactions that range from a slight improvement in yield to the complete cessation of the reaction. In contrast, palladium does not interact sufficiently strongly with these functional groups to induce selectivity in cross-coupling reactions; the selectivity of palladium-catalysed cross-coupling reactions is predominantly governed by aryl halide electronic properties

    A constrained Potts antiferromagnet model with an interface representation

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    We define a four-state Potts model ensemble on the square lattice, with the constraints that neighboring spins must have different values, and that no plaquette may contain all four states. The spin configurations may be mapped into those of a 2-dimensional interface in a 2+5 dimensional space. If this interface is in a Gaussian rough phase (as is the case for most other models with such a mapping), then the spin correlations are critical and their exponents can be related to the stiffness governing the interface fluctuations. Results of our Monte Carlo simulations show height fluctuations with an anomalous dependence on wavevector, intermediate between the behaviors expected in a rough phase and in a smooth phase; we argue that the smooth phase (which would imply long-range spin order) is the best interpretation.Comment: 61 pages, LaTeX. Submitted to J. Phys.

    Integration of genetics into a systems model of electrocardiographic traits using humanCVD BeadChip

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    <p>Background—Electrocardiographic traits are important, substantially heritable determinants of risk of arrhythmias and sudden cardiac death.</p> <p>Methods and Results—In this study, 3 population-based cohorts (n=10 526) genotyped with the Illumina HumanCVD Beadchip and 4 quantitative electrocardiographic traits (PR interval, QRS axis, QRS duration, and QTc interval) were evaluated for single-nucleotide polymorphism associations. Six gene regions contained single nucleotide polymorphisms associated with these traits at P<10−6, including SCN5A (PR interval and QRS duration), CAV1-CAV2 locus (PR interval), CDKN1A (QRS duration), NOS1AP, KCNH2, and KCNQ1 (QTc interval). Expression quantitative trait loci analyses of top associated single-nucleotide polymorphisms were undertaken in human heart and aortic tissues. NOS1AP, SCN5A, IGFBP3, CYP2C9, and CAV1 showed evidence of differential allelic expression. We modeled the effects of ion channel activity on electrocardiographic parameters, estimating the change in gene expression that would account for our observed associations, thus relating epidemiological observations and expression quantitative trait loci data to a systems model of the ECG.</p> <p>Conclusions—These association results replicate and refine the mapping of previous genome-wide association study findings for electrocardiographic traits, while the expression analysis and modeling approaches offer supporting evidence for a functional role of some of these loci in cardiac excitation/conduction.</p&gt

    The Ursinus Weekly, April 18, 1949

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    Council adopts petitions for \u2749 coed elections • Junior men to elect annual prom queen • Black-faced belles plan initial debut for minstrel frolic • Organizations seek support of students in worthy projects • Y commission lists letters, trip, talk in year\u27s activities • Sororities plan party for frosh; Movie, social to highlight affair • FTA elects Heist to presidency for \u2749-\u2750 schedule of activities • What do you demand of your ideal man? • Bruins drop 4-3 decision in ten inning ball game • Five sports events fill week\u27s roster • Sixteen get awards for winter sports • Students find appeal in Curtain Club actshttps://digitalcommons.ursinus.edu/weekly/1614/thumbnail.jp

    Vortex Images and q-Elementary Functions

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    In the present paper problem of vortex images in annular domain between two coaxial cylinders is solved by the q-elementary functions. We show that all images are determined completely as poles of the q-logarithmic function, where dimensionless parameter q=r22/r12q = r^2_2/r^2_1 is given by square ratio of the cylinder radii. Resulting solution for the complex potential is represented in terms of the Jackson q-exponential function. By composing pairs of q-exponents to the first Jacobi theta function and conformal mapping to a rectangular domain we link our solution with result of Johnson and McDonald. We found that one vortex cannot remain at rest except at the geometric mean distance, but must orbit the cylinders with constant angular velocity related to q-harmonic series. Vortex images in two particular geometries in the qq \to \infty limit are studied.Comment: 17 page

    Placental Structure in Type 1 Diabetes: Relation to Fetal Insulin, Leptin, and IGF-I

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    OBJECTIVE-Alteration of placental structure may influence fetal overgrowth and complications of maternal diabetes. We examined the placenta in a cohort of offspring of mothers with type I diabetes (OT1DM) to assess structural changes and determine whether these were related to maternal A1C, fetal hematocrit, fetal hormonal, or metabolic axes. RESEARCH DESIGN AND METHODS-Placental samples were analyzed using stereological techniques to quantify volumes and surface areas of key placental components in 88 OT1DM and 39 control subjects, and results related to maternal A1C and umbilical cord analytes (insulin, leptin, adiponectin, IGF-I, hematocrit, lipids, C-reactive protein, and interleukin-6). RESULTS-Intervillous space volume was increased in OT1DM (OT1DM 250 +/- 81 cm(3) VS. control 217 +/- 65 cm(3); P = 0.02) with anisomorphic growth of villi (P = 0.025). The placentas showed a trend to increased weight (OT1DM 690 +/- 19 g; control 641 +/- 22 g; P = 0.08), but villous, nonparenchymal, trophoblast, and capillary volumes did not differ. Villous surface area, capillary surface area, membrane thickness, and calculated morphometric diffusing capacity were also similar in type 1 diabetic and control subjects. A1C at 26-34 weeks associated with birth weight (r = 0.27, P = 0.03), placental weight (r = 0.41, P = 0.0009), and intervillous space volume (r = 0.38, P = 0.0024). In multivariate analysis of cord parameters in OT1DM, fetal IGF-I emerged as a significant correlate of most components (intervillous space, villous, trophoblast, and capillary volumes, all P < 0.01). By contrast, fetal insulin was only independently associated with capillary surface area (positive, r(2) = 6.7%; P = 0.02). CONCLUSIONS-There are minimal placental structural differences between OT1DM and control subjects. Fetal IGF-I but not fetal insulin emerges as a key correlate of placental substructural volumes, thereby facilitating feedback to the placenta regarding fetal metabolic deman

    Efficacy and safety of enzyme replacement therapy with BMN 110 (elosulfase alfa) for Morquio A syndrome (mucopolysaccharidosis IVA): a phase 3 randomised placebo-controlled study.

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    ObjectiveTo assess the efficacy and safety of enzyme replacement therapy (ERT) with BMN 110 (elosulfase alfa) in patients with Morquio A syndrome (mucopolysaccharidosis IVA).MethodsPatients with Morquio A aged ≥5 years (N = 176) were randomised (1:1:1) to receive elosulfase alfa 2.0 mg/kg/every other week (qow), elosulfase alfa 2.0 mg/kg/week (weekly) or placebo for 24 weeks in this phase 3, double-blind, randomised study. The primary efficacy measure was 6-min walk test (6MWT) distance. Secondary efficacy measures were 3-min stair climb test (3MSCT) followed by change in urine keratan sulfate (KS). Various exploratory measures included respiratory function tests. Patient safety was also evaluated.ResultsAt week 24, the estimated mean effect on the 6MWT versus placebo was 22.5 m (95 % CI 4.0, 40.9; P = 0.017) for weekly and 0.5 m (95 % CI -17.8, 18.9; P = 0.954) for qow. The estimated mean effect on 3MSCT was 1.1 stairs/min (95 % CI -2.1, 4.4; P = 0.494) for weekly and -0.5 stairs/min (95 % CI -3.7, 2.8; P = 0.778) for qow. Normalised urine KS was reduced at 24 weeks in both regimens. In the weekly dose group, 22.4 % of patients had adverse events leading to an infusion interruption/discontinuation requiring medical intervention (only 1.3 % of all infusions in this group) over 6 months. No adverse events led to permanent treatment discontinuation.ConclusionsElosulfase alfa improved endurance as measured by the 6MWT in the weekly but not qow dose group, did not improve endurance on the 3MSCT, reduced urine KS, and had an acceptable safety profile

    Cost-effectiveness of financial incentives to promote adherence to depot antipsychotic medication: economic evaluation of a cluster-randomised controlled trial

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    Background: Offering a modest financial incentive to people with psychosis can promote adherence to depot antipsychotic medication, but the cost-effectiveness of this approach has not been examined. Methods: Economic evaluation within a pragmatic cluster-randomised controlled trial. 141 patients under the care of 73 teams (clusters) were randomised to intervention or control; 138 patients with diagnoses of schizophrenia, schizo-affective disorder or bipolar disorder participated. Intervention participants received £15 per depot injection over 12 months, additional to usual acute, mental and community primary health services. The control group received usual health services. Main outcome measures: incremental cost per 20% increase in adherence to depot antipsychotic medication; incremental cost of ‘good’ adherence (defined as taking at least 95% of the prescribed number of depot medications over the intervention period). Findings: Economic and outcome data for baseline and 12-month follow-up were available for 117 participants. The adjusted difference in adherence between groups was 12.2% (73.4% control vs. 85.6% intervention); the adjusted costs difference was £598 (95% CI -£4 533, £5 730). The extra cost per patient to increase adherence to depot medications by 20% was £982 (95% CI -£8 020, £14 000). The extra cost per patient of achieving 'good' adherence was £2 950 (CI -£19 400, £27 800). Probability of cost-effectiveness exceeded 97.5%at willingness-to-pay values of £14 000 for a 20% increase in adherence and £27 800 for good adherence. Interpretation: Offering a modest financial incentive to people with psychosis is cost-effective in promoting adherence to depot antipsychotic medication. Direct healthcare costs (including costs of the financial incentive) are unlikely to be increased by this intervention. Trial Registration: ISRCTN.com 7776928
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