25,422 research outputs found

    Tweeting with Bae: a Corpus Analysis of the Recent Lexical Item Bae

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    Parasitism of \u3ci\u3ePlathypena Scabra\u3c/i\u3e (Lepidoptera: Noctuidae) by \u3ci\u3eSinophorus Teratis\u3c/i\u3e (Hymenoptera: Ichneumonidae)

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    (excerpt) A study was conducted at the Ecology Research Center, Miami University, Butler County, Ohio, during the summer of 1990 to examine the effects of strip intercropping sorghum and soybean on the occurrence of parasitoids and incidence of disease in larvae ofthe green cloverworm, Plathypena scabra (F.) (Lepidoptera: Noctuidae), a sporadic pest of soybeans. The details of the experimental design and results are reported elsewhere (Williams et al. 1995)

    Genetic testing for Familial Hypercholesterolaemia - Past, Present and Future

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    In the early 1980s, the Nobel Prize winning cellular and molecular work of Mike Brown and Joe Goldstein led to the identification of the Low Density Lipoprotein Receptor (LDLR) gene as the first gene where mutations cause the Familial Hypercholesterolaemia (FH) phenotype. We now know that autosomal dominant monogenic FH can be caused by pathogenic variants of three additional genes (APOB/PCSK9/APOE), and that the plasma LDL-C concentration and risk of premature Coronary Heart Disease (CHD) differs according to the specific locus and associated molecular cause. It is now possible to use Next Generation Sequencing (NGS) to sequence all exons of all four genes, processing 96 patient samples in one sequencing run, increasing the speed of test results and reducing costs. This has resulted in the identification of many novel FH-causing variants, but also some "Variants of Unknown Significance (VUSs)" which require further evidence to classify as pathogenic or benign. The identification of the FH-causing variant in an index case can be used as an unambiguous and rapid test for other family members. An FH-causing variant can be found in 20%-40% of patients with the FH phenotype, and we now appreciate that in the majority of patients without a monogenic cause, a polygenic aetiology for their phenotype is highly likely. Compared to those with a monogenic cause, these patients have significantly lower risk of future CHD. The use of these molecular genetic diagnostic methods in the characterization of FH is a prime example of the utility of precision or personalised medicine

    Invisible, Underserved, and Diverse: The Health of Women in Prison

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    In the United States of America, women are the fastest growing segment of the criminal justice system. They are entering the system with far greater physical and mental health problems than men, but with fewer health services. Additionally, within this expanding population of incarcerated women, are disproportionately represented poor women of color with serious health needs. This article: a) uses an ecosocial model to examine and critique the health and healthcare of women in prison, b) examines social structures that influence incarceration and health status, and c) proposes reconsideration of current prison health services and education

    The EXOSAT medium-energy slew survey catalog

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    We present a catalog of X-ray sources observed during slew maneuvers by the Medium Energy Detector Array onboard the EXOSAT Observatory. The EXOSAT Medium Energy slew-survey catalog (EXMS) provides a unique record of the 1--8 keV X-ray sky between 1983 and 1986. 98% of the sky was observed, with 85% receiving an exposure of >60 s. 1210 sources were detected. By comparing these source positions with other catalogs, identifications are given for 992 detections (82% of the sample). These identifications consist of 250 distinct objects, including 95 different X-ray binary systems, and 14 different AGN. A further 58 detections have multiple candidates, while 160 detections remain unidentified. Collimator transmission corrected 1-8 keV count rates are given for the identified sources, together with raw count rates for the other detections. The construction of the EXMS and the checks performed to ensure the validity of the derived source properties are discussed. A publically available version of this catalog is maintained on the EXOSAT database and archive system (telnet://[email protected]).Comment: 52 pages. 22 Figures. To be published in A&AS. For more information, see http://astro.estec.esa.nl/SA-general/Projects/Exosat/exmsintro.htm
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