689 research outputs found

    Carbonated Drinks Impact Follicle Development, Expression of Ovarian FSHR and Serum Caspase-3 in Mice

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    Objectives: The present study aimed to assess the effects of Coca-Cola and Pepsi-Cola on the development of ovaries and follicles, and on the reproduction of animals

    A WSN approach to unmanned aerial surveillance of traffic anomalies: Some challenges and potential solutions

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    Stationary CCTV cameras are often used to help monitor car movements and detect any anomalies - e.g., accidents, cars going faster than the allowed speed, driving under the influence of alcohol, etc. The height of the cameras can limit their effectiveness and the types of image processing algorithm which can be used. With advancements in the development of inexpensive aerial flying objects and wireless devices, these two technologies can be coupled to support enhanced surveillance. The flying objects can carry multiple cameras and be sent well above the ground to capture and feed video/image information back to a ground station. In addition, because of the height the objects can achieve, they can capture videos and images which could lend themselves more suitably for the application of a variety of video and image processing algorithms to assist analysts in detecting any anomalies. In this paper, we examine some main challenges of using flying objects for surveillance purposes and propose some potential solutions to these challenges. By doing so, we attempt to provide the basis for developing a framework to build a viable system for improved surveillance based on low-cost equipment. © 2013 IEEE.t.published_or_final_versio

    Coronary artery fistula; coronary computed topography – The diagnostic modality of choice

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    Coronary artery fistulae (CAF) are rare anomalies. They are vascular communications between the coronary arteries and other cardiac structures, either cardiac chambers or great vessels. There can be considerable variation in the course of a coronary artery fistula. We report a case of a coronary artery fistula between the left circumflex coronary artery and the right and left atria. CAF are often diagnosed by coronary angiogram, however with the advent of new technologies such as Coronary Computed Tomography Angiography (Coronary CTA) the course and communications of these fistulae can be delineated non-invasively and with greater accuracy

    Pre- and early-postnatal nutrition modify gene and protein expressions of muscle energy metabolism markers and phospholipid fatty acid composition in a muscle type specific manner in sheep.

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    We previously reported that undernutrition in late fetal life reduced whole-body insulin sensitivity in adult sheep, irrespective of dietary exposure in early postnatal life. Skeletal muscle may play an important role in control of insulin action. We therefore studied a range of putative key muscle determinants of insulin signalling in two types of skeletal muscles (longissimus dorsi (LD) and biceps femoris (BF)) and in the cardiac muscle (ventriculus sinister cordis (VSC)) of sheep from the same experiment. Twin-bearing ewes were fed either 100% (NORM) or 50% (LOW) of their energy and protein requirements during the last trimester of gestation. From day-3 postpartum to 6-months of age (around puberty), twin offspring received a high-carbohydrate-high-fat (HCHF) or a moderate-conventional (CONV) diet, whereafter all males were slaughtered. Females were subsequently raised on a moderate diet and slaughtered at 2-years of age (young adults). The only long-term consequences of fetal undernutrition observed in adult offspring were lower expressions of the insulin responsive glucose transporter 4 (GLUT4) protein and peroxisome proliferator-activated receptor gamma, coactivator 1α (PGC1α) mRNA in BF, but increased PGC1α expression in VSC. Interestingly, the HCHF diet in early postnatal life was associated with somewhat paradoxically increased expressions in LD of a range of genes (but not proteins) related to glucose uptake, insulin signalling and fatty acid oxidation. Except for fatty acid oxidation genes, these changes persisted into adulthood. No persistent expression changes were observed in BF and VSC. The HCHF diet increased phospholipid ratios of n-6/n-3 polyunsaturated fatty acids in all muscles, even in adults fed identical diets for 1½ years. In conclusion, early postnatal, but not late gestation, nutrition had long-term consequences for a number of determinants of insulin action and metabolism in LD. Tissues other than muscle may account for reduced whole body insulin sensitivity in adult LOW sheep

    Measurement of the proton form factor by studying e+eppˉe^{+} e^{-}\rightarrow p\bar{p}

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    Using data samples collected with the BESIII detector at the BEPCII collider, we measure the Born cross section of e+eppˉe^{+}e^{-}\rightarrow p\bar{p} at 12 center-of-mass energies from 2232.4 to 3671.0 MeV. The corresponding effective electromagnetic form factor of the proton is deduced under the assumption that the electric and magnetic form factors are equal (GE=GM)(|G_{E}|= |G_{M}|). In addition, the ratio of electric to magnetic form factors, GE/GM|G_{E}/G_{M}|, and GM|G_{M}| are extracted by fitting the polar angle distribution of the proton for the data samples with larger statistics, namely at s=\sqrt{s}= 2232.4 and 2400.0 MeV and a combined sample at s\sqrt{s} = 3050.0, 3060.0 and 3080.0 MeV, respectively. The measured cross sections are in agreement with recent results from BaBar, improving the overall uncertainty by about 30\%. The GE/GM|G_{E}/G_{M}| ratios are close to unity and consistent with BaBar results in the same q2q^{2} region, which indicates the data are consistent with the assumption that GE=GM|G_{E}|=|G_{M}| within uncertainties.Comment: 13 pages, 24 figure

    Observation of the isospin-violating decay J/ψϕπ0f0(980)J/\psi \to \phi\pi^{0}f_{0}(980)

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    Using a sample of 1.31 billion J/ψJ/\psi events collected with the BESIII detector at the BEPCII collider, the decays J/ψϕπ+ππ0J/\psi \to \phi \pi^{+}\pi^{-}\pi^{0} and J/ψϕπ0π0π0J/\psi \to \phi \pi^{0}\pi^{0}\pi^{0} are investigated. The isospin violating decay J/ψϕπ0f0(980)J/\psi \to \phi \pi^{0} f_{0}(980) with f0(980)ππf_{0}(980) \to \pi\pi, is observed for the first time. The width of the f0(980)f_{0}(980) obtained from the dipion mass spectrum is found to be much smaller than the world average value. In the π0f0(980)\pi^{0} f_{0}(980) mass spectrum, there is evidence of f1(1285)f_1(1285) production. By studying the decay J/ψϕηJ/\psi \to \phi\eta', the branching fractions of ηπ+ππ0\eta' \to \pi^{+}\pi^{-}\pi^{0} and ηπ0π0π0\eta' \to \pi^{0}\pi^{0}\pi^{0}, as well as their ratio, are also measured.Comment: 10 pages, 10 figures, published in Phys. Rev.

    An amplitude analysis of the π0π0\pi^{0}\pi^{0} system produced in radiative J/ψJ/\psi decays

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    An amplitude analysis of the π0π0\pi^{0}\pi^{0} system produced in radiative J/ψJ/\psi decays is presented. In particular, a piecewise function that describes the dynamics of the π0π0\pi^{0}\pi^{0} system is determined as a function of Mπ0π0M_{\pi^{0}\pi^{0}} from an analysis of the (1.311±0.011)×109(1.311\pm0.011)\times10^{9} J/ψJ/\psi decays collected by the BESIII detector. The goal of this analysis is to provide a description of the scalar and tensor components of the π0π0\pi^0\pi^0 system while making minimal assumptions about the properties or number of poles in the amplitude. Such a model-independent description allows one to integrate these results with other related results from complementary reactions in the development of phenomenological models, which can then be used to directly fit experimental data to obtain parameters of interest. The branching fraction of J/ψγπ0π0J/\psi \to \gamma \pi^{0}\pi^{0} is determined to be (1.15±0.05)×103(1.15\pm0.05)\times10^{-3}, where the uncertainty is systematic only and the statistical uncertainty is negligible.Comment: Submitted to Phys. Rev. D 19 pages, 4 figure

    Global, regional, and national comparative risk assessment of 79 behavioural, environmental and occupational, and metabolic risks or clusters of risks, 1990-2015: a systematic analysis for the Global Burden of Disease Study 2015

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    SummaryBackground The Global Burden of Diseases, Injuries, and Risk Factors Study 2015 provides an up-to-date synthesis of the evidence for risk factor exposure and the attributable burden of disease. By providing national and subnational assessments spanning the past 25 years, this study can inform debates on the importance of addressing risks in context. Methods We used the comparative risk assessment framework developed for previous iterations of the Global Burden of Disease Study to estimate attributable deaths, disability-adjusted life-years (DALYs), and trends in exposure by age group, sex, year, and geography for 79 behavioural, environmental and occupational, and metabolic risks or clusters of risks from 1990 to 2015. This study included 388 risk-outcome pairs that met World Cancer Research Fund-defined criteria for convincing or probable evidence. We extracted relative risk and exposure estimates from randomised controlled trials, cohorts, pooled cohorts, household surveys, census data, satellite data, and other sources. We used statistical models to pool data, adjust for bias, and incorporate covariates. We developed a metric that allows comparisons of exposure across risk factors—the summary exposure value. Using the counterfactual scenario of theoretical minimum risk level, we estimated the portion of deaths and DALYs that could be attributed to a given risk. We decomposed trends in attributable burden into contributions from population growth, population age structure, risk exposure, and risk-deleted cause-specific DALY rates. We characterised risk exposure in relation to a Socio-demographic Index (SDI). Findings Between 1990 and 2015, global exposure to unsafe sanitation, household air pollution, childhood underweight, childhood stunting, and smoking each decreased by more than 25%. Global exposure for several occupational risks, high body-mass index (BMI), and drug use increased by more than 25% over the same period. All risks jointly evaluated in 2015 accounted for 57·8% (95% CI 56·6–58·8) of global deaths and 41·2% (39·8–42·8) of DALYs. In 2015, the ten largest contributors to global DALYs among Level 3 risks were high systolic blood pressure (211·8 million [192·7 million to 231·1 million] global DALYs), smoking (148·6 million [134·2 million to 163·1 million]), high fasting plasma glucose (143·1 million [125·1 million to 163·5 million]), high BMI (120·1 million [83·8 million to 158·4 million]), childhood undernutrition (113·3 million [103·9 million to 123·4 million]), ambient particulate matter (103·1 million [90·8 million to 115·1 million]), high total cholesterol (88·7 million [74·6 million to 105·7 million]), household air pollution (85·6 million [66·7 million to 106·1 million]), alcohol use (85·0 million [77·2 million to 93·0 million]), and diets high in sodium (83·0 million [49·3 million to 127·5 million]). From 1990 to 2015, attributable DALYs declined for micronutrient deficiencies, childhood undernutrition, unsafe sanitation and water, and household air pollution; reductions in risk-deleted DALY rates rather than reductions in exposure drove these declines. Rising exposure contributed to notable increases in attributable DALYs from high BMI, high fasting plasma glucose, occupational carcinogens, and drug use. Environmental risks and childhood undernutrition declined steadily with SDI; low physical activity, high BMI, and high fasting plasma glucose increased with SDI. In 119 countries, metabolic risks, such as high BMI and fasting plasma glucose, contributed the most attributable DALYs in 2015. Regionally, smoking still ranked among the leading five risk factors for attributable DALYs in 109 countries; childhood underweight and unsafe sex remained primary drivers of early death and disability in much of sub-Saharan Africa. Interpretation Declines in some key environmental risks have contributed to declines in critical infectious diseases. Some risks appear to be invariant to SDI. Increasing risks, including high BMI, high fasting plasma glucose, drug use, and some occupational exposures, contribute to rising burden from some conditions, but also provide opportunities for intervention. Some highly preventable risks, such as smoking, remain major causes of attributable DALYs, even as exposure is declining. Public policy makers need to pay attention to the risks that are increasingly major contributors to global burden. Funding Bill & Melinda Gates Foundation

    Anastral spindle assembly and γ-tubulin in Drosophila oocytes

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    <p>Abstract</p> <p>Background</p> <p>Anastral spindles assemble by a mechanism that involves microtubule nucleation and growth from chromatin. It is still uncertain whether γ-tubulin, a microtubule nucleator essential for mitotic spindle assembly and maintenance, plays a role. Not only is the requirement for γ-tubulin to form anastral <it>Drosophila </it>oocyte meiosis I spindles controversial, but its presence in oocyte meiosis I spindles has not been demonstrated and is uncertain.</p> <p>Results</p> <p>We show, for the first time, using a bright GFP fusion protein and live imaging, that the <it>Drosophila </it>maternally-expressed γTub37C is present at low levels in oocyte meiosis I spindles. Despite this, we find that formation of bipolar meiosis I spindles does not require functional γTub37C, extending previous findings by others. Fluorescence photobleaching assays show rapid recovery of γTub37C in the meiosis I spindle, similar to the cytoplasm, indicating weak binding by γTub37C to spindles, and fits of a new, potentially more accurate model for fluorescence recovery yield kinetic parameters consistent with transient, diffusional binding.</p> <p>Conclusions</p> <p>The FRAP results, together with its mutant effects late in meiosis I, indicate that γTub37C may perform a role subsequent to metaphase I, rather than nucleating microtubules for meiosis I spindle formation. Weak binding to the meiosis I spindle could stabilize pre-existing microtubules or position γ-tubulin for function during meiosis II spindle assembly, which follows rapidly upon oocyte activation and completion of the meiosis I division.</p
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