2,839 research outputs found

    High Transverse Momentum Physics at the Large Hadron Collider

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    This note summarizes many detailed physics studies done by the ATLAS and CMS Collaborations for the LHC, concentrating on processes involving the production of high mass states. These studies show that the LHC should be able to elucidate the mechanism of electroweak symmetry breaking and to study a variety of other topics related to physics at the TeV scale. In particular, a Higgs boson with couplings given by the Standard Model is observable in several channels over the full range of allowed masses. Its mass and some of its couplings will be determined. If supersymmetry is relevant to electroweak interactions, it will be discovered and the properties of many supersymmetric particles elucidated. Other new physics, such as the existence of massive gauge bosons and extra dimensions can be searched for extending existing limits by an order of magnitude or more.Comment: Authors listed are the editor

    Cardiac dysfunction in the diabetic rat: quantitative evaluation using high resolution magnetic resonance imaging

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    BACKGROUND: Diabetes is a major risk factor for cardiovascular disease. In particular, type 1 diabetes compromises the cardiac function of individuals at a relatively early age due to the protracted course of abnormal glucose homeostasis. The functional abnormalities of diabetic myocardium have been attributed to the pathological changes of diabetic cardiomyopathy. METHODS: In this study, we used high field magnetic resonance imaging (MRI) to evaluate the left ventricular functional characteristics of streptozotocin treated diabetic Sprague-Dawley rats (8 weeks disease duration) in comparison with age/sex matched controls. RESULTS: Our analyses of EKG gated cardiac MRI scans of the left ventricle showed a 28% decrease in the end-diastolic volume and 10% increase in the end-systolic volume of diabetic hearts compared to controls. Mean stroke volume and ejection fraction in diabetic rats were decreased (48% and 28%, respectively) compared to controls. Further, dV/dt changes were suggestive of phase sensitive differences in left ventricular kinetics across the cardiac cycle between diabetic and control rats. CONCLUSION: Thus, the MRI analyses of diabetic left ventricle suggest impairment of diastolic and systolic hemodynamics in this rat model of diabetic cardiomyopathy. Our studies also show that in vivo MRI could be used in the evaluation of cardiac dysfunction in this rat model of type 1 diabetes

    Resistance exercise training lowers HbA1c more than aerobic training in adults with type 2 diabetes

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    <p>Abstract</p> <p>Background</p> <p>The aim of this study was to compare the effects of 10 weeks of resistance or treadmill exercises on glycemic indices levels prior to and immediately following exercise in adults with type 2 diabetes.</p> <p>Research Design and Method</p> <p>Twenty inactive subjects (mean age 53.5 years) with type 2 diabetes enrolled in the study. Baseline HbA1c, blood glucose levels, heart rate, and blood pressure were measured for each subject prior to the initiation of the exercise program. Subsequently, subjects were matched to age, waist circumference and sex and assigned to either isocaloric resistance or treadmill exercise groups, which met 3 times per week for 10 weeks.</p> <p>Results</p> <p>Both groups showed a reduction in pre and post-exercise blood glucose and HbA1c values. There was no change in resting blood pressure or heart rate in either group during the course of the 10 week intervention. The group receiving resistance exercises showed significant differences in the daily pre-exercise plasma glucose readings between the beginning and end of the exercise protocol (p < 0.001). There were significant improvements in the mean HbA1c reading pre and post training in both groups (p < 0.001). However, the greater reduction was noted in the resistance exercise group, and at 10 weeks their HbA1c levels were significantly lower than the group that received treadmill exercises (p < 0.006).</p> <p>Conclusion</p> <p>Ten weeks of resistance exercises were associated with a significantly better glycemic control in adults with type 2 diabetes compared to treadmill exercise.</p

    Variations in Daily Maximum Areas and Longitudinal Widths of Solar Coronal Holes in 2017-2020

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    We considered coronal holes as a manifestation of the large-scale magnetic field of the Sun. The main goal of this work was to study the variations in the largest areas and longitudinal widths of solar coronal holes observed daily in the polar and mid-latitude zones on a time scale of 984 days. Statistical methods of fast Fourier transform (FFT), wavelet transform, and empirical mode decomposition (EMD) were used to detect periodicity in the variations of the considered parameters. Long-term variations in the daily measured areas and longitudinal widths of the largest solar coronal holes with periods of 8-9,13-15, and 26-29 days were detected in three zones of the Sun: polar (north and south) and equatorial. The obtained periods are most clearly visible at the equatorial zone. In the polar zones the period of 8-9 days has a weak amplitude. We interpreted variations with periods of 8-9,13-15, and 26-29 days as a rotation of the six-, four-, and two-sector structure of the large-scale solar magnetic field

    Spectroscopy of 18^{18}Na: Bridging the two-proton radioactivity of 19^{19}Mg

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    The unbound nucleus 18^{18}Na, the intermediate nucleus in the two-proton radioactivity of 19^{19}Mg, was studied by the measurement of the resonant elastic scattering reaction 17^{17}Ne(p,17^{17}Ne)p performed at 4 A.MeV. Spectroscopic properties of the low-lying states were obtained in a R-matrix analysis of the excitation function. Using these new results, we show that the lifetime of the 19^{19}Mg radioactivity can be understood assuming a sequential emission of two protons via low energy tails of 18^{18}Na resonances

    Emerging Priorities for Microbiome Research

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    Microbiome research has increased dramatically in recent years, driven by advances in technology and significant reductions in the cost of analysis. Such research has unlocked a wealth of data, which has yielded tremendous insight into the nature of the microbial communities, including their interactions and effects, both within a host and in an external environment as part of an ecological community. Understanding the role of microbiota, including their dynamic interactions with their hosts and other microbes, can enable the engineering of new diagnostic techniques and interventional strategies that can be used in a diverse spectrum of fields, spanning from ecology and agriculture to medicine and from forensics to exobiology. From June 19–23 in 2017, the NIH and NSF jointly held an Innovation Lab on Quantitative Approaches to Biomedical Data Science Challenges in our Understanding of the Microbiome. This review is inspired by some of the topics that arose as priority areas from this unique, interactive workshop. The goal of this review is to summarize the Innovation Lab’s findings by introducing the reader to emerging challenges, exciting potential, and current directions in microbiome research. The review is broken into five key topic areas: (1) interactions between microbes and the human body, (2) evolution and ecology of microbes, including the role played by the environment and microbe-microbe interactions, (3) analytical and mathematical methods currently used in microbiome research, (4) leveraging knowledge of microbial composition and interactions to develop engineering solutions, and (5) interventional approaches and engineered microbiota that may be enabled by selectively altering microbial composition. As such, this review seeks to arm the reader with a broad understanding of the priorities and challenges in microbiome research today and provide inspiration for future investigation and multi-disciplinary collaboration

    Separating chemotherapy-related developmental neurotoxicity from cytotoxicity in monolayer and neurosphere cultures of human fetal brain cells

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    Chemotherapy-induced neurotoxicity can reduce the quality of life of patients by affecting their intelligence, senses and mobility. Ten percent of safety-related late-stage clinical failures are due to neurological side effects. Animal models are poor in predicting human neurotoxicity due to interspecies differences and most in vitro assays cannot distinguish neurotoxicity from general cytotoxicity for chemotherapeutics. We developed in vitro assays capable of quantifying the paediatric neurotoxic potential for cytotoxic drugs. Mixed cultures of human fetal brain cells were differentiated in monolayers and as 3D-neurospheres in the presence of non-neurotoxic chemotherapeutics (etoposide, teniposide) or neurotoxicants (methylmercury). The cytotoxic potency towards dividing progenitors versus differentiated neurons and astrocytes was compared using: (1) immunohistochemistry staining and cell counts in monolayers; (2) through quantitative Western blots in neurospheres; and (3) neurosphere migration assays. Etoposide and teniposide, were 5–10 times less toxic to differentiated neurons compared to the mix of all cells in monolayer cultures. In contrast, the neurotoxicant methylmercury did not exhibit selectivity and killed all cells with the same potency. In 3D neurospheres, etoposide and teniposide were 24 to 10 times less active against neurons compared to all cells. These assays can be used prioritise drugs for local drug delivery to brain tumours
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