260 research outputs found

    Feminism as "piffling"? Ambiguities in Nadine Gordimer's short stories

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    Paper presented at the Wits History Workshop: Structure and Experience in the Making of Apartheid, 6-10 February, 1990

    Open-ocean submesoscale motions: a full seasonal cycle of mixed layer instabilities from gliders

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    The importance of submesoscale instabilities, particularly mixed-layer baroclinic instability and symmetric instability, on upper ocean mixing and energetics is well documented in regions of strong, persistent fronts such as the Kuroshio and the Gulf Stream. Less attention has been devoted to studying submesoscale flows in the open ocean, far from long-term mean geostrophic fronts, characteristic of a large proportion of the global ocean. We present a year-long, submesoscale-resolving time series of near-surface buoyancy gradients, potential vorticity and instability characteristics, collected by ocean gliders, that provides insight into open-ocean submesoscale dynamics over a full annual cycle. The gliders continuously sampled a 225 km2 region in the subtropical northeast Atlantic, measuring temperature, salinity and pressure along 292 short (\~{}20 km) hydrographic sections.Glider observations show a seasonal cycle in near-surface stratification. Throughout the fall (September through November), the mixed layer deepens, predominantly through gravitational instability, indicating that surface cooling dominates submesoscale restratification processes. During winter (December through March), mixed layer depths are more variable, and estimates of the balanced Richardson number, which measures the relative importance of lateral and vertical buoyancy gradients, depict conditions favorable to symmetric instability. The importance of mixed layer instabilities on the restratification of the mixed layer, as compared with surface heating and cooling, shows that submesoscale processes can reverse the sign of an equivalent heat flux up to 25{\%} of the time during winter. These results demonstrate that the open-ocean mixed layer hosts various forced and unforced instabilities, which become more prevalent during winter, and emphasize that accurate parameterizations of submesoscale processes are needed throughout the ocean

    The Grizzly, January 30, 1981

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    Gambling Investigation Prompts Student Withdrawals ‱ Thornburgh Discusses Education At Conference ‱ Todd Hall Fined $200 For Alcohol Violation ‱ Tower Restoration Scheduled ‱ McQuillan Presents Financial Aid Workshop ‱ Magazine Addresses Students ‱ J-Board Workings Explained By Barth ‱ Fraternity Theories ‱ Bids Distribution ‱ Top Ten Albums of 1980 ‱ Greaseband Unable To Return This Semester ‱ Spiritwood: A Different Coffeehouse ‱ Theatre: A Midsummer Night\u27s Dream ‱ Shipping Delay Postpones NMD Window Installation ‱ Departmental Focus: Health And Physical Education ‱ Swim Coach Hopes For .500 Season ‱ Men\u27s Basketball Holding 1st Place In MAC ‱ Grapplers Having An Up & Down Year ‱ Haag Leads Lady Hoopsters Past Widenerhttps://digitalcommons.ursinus.edu/grizzlynews/1050/thumbnail.jp

    Defining Optimal Brain Health in Adults A Presidential Advisory From the American Heart Association/American Stroke Association

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    Cognitive function is an important component of aging and predicts quality of life, functional independence, and risk of institutionalization. Advances in our understanding of the role of cardiovascular risks have shown them to be closely associated with cognitive impairment and dementia. Because many cardiovascular risks are modifiable, it may be possible to maintain brain health and to prevent dementia in later life. The purpose of this American Heart Association (AHA)/American Stroke Association presidential advisory is to provide an initial definition of optimal brain health in adults and guidance on how to maintain brain health. We identify metrics to define optimal brain health in adults based on inclusion of factors that could be measured, monitored, and modified. From these practical considerations, we identified 7 metrics to define optimal brain health in adults that originated from AHA's Life's Simple 7: 4 ideal health behaviors (nonsmoking, physical activity at goal levels, healthy diet consistent with current guideline levels, and body mass index < 25 kg/m(2)) and 3 ideal health factors (untreated blood pressure < 120/< 80 mm Hg, untreated total cholesterol < 200 mg/dL, and fasting blood glucose < 100 mg/dL). In addition, in relation to maintenance of cognitive health, we recommend following previously published guidance from the AHA/American Stroke Association, Institute of Medicine, and Alzheimer's Association that incorporates control of cardiovascular risks and suggest social engagement and other related strategies. We define optimal brain health but recognize that the truly ideal circumstance may be uncommon because there is a continuum of brain health as demonstrated by AHA's Life's Simple 7. Therefore, there is opportunity to improve brain health through primordial prevention and other interventions. Furthermore, although cardiovascular risks align well with brain health, we acknowledge that other factors differing from those related to cardiovascular health may drive cognitive health. Defining optimal brain health in adults and its maintenance is consistent with the AHA's Strategic Impact Goal to improve cardiovascular health of all Americans by 20% and to reduce deaths resulting from cardiovascular disease and stroke by 20% by the year 2020. This work in defining optimal brain health in adults serves to provide the AHA/American Stroke Association with a foundation for a new strategic direction going forward in cardiovascular health promotion and disease prevention

    Genomic, Pathway Network, and Immunologic Features Distinguishing Squamous Carcinomas

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    This integrated, multiplatform PanCancer Atlas study co-mapped and identified distinguishing molecular features of squamous cell carcinomas (SCCs) from five sites associated with smokin

    Spatial Organization and Molecular Correlation of Tumor-Infiltrating Lymphocytes Using Deep Learning on Pathology Images

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    Beyond sample curation and basic pathologic characterization, the digitized H&E-stained images of TCGA samples remain underutilized. To highlight this resource, we present mappings of tumorinfiltrating lymphocytes (TILs) based on H&E images from 13 TCGA tumor types. These TIL maps are derived through computational staining using a convolutional neural network trained to classify patches of images. Affinity propagation revealed local spatial structure in TIL patterns and correlation with overall survival. TIL map structural patterns were grouped using standard histopathological parameters. These patterns are enriched in particular T cell subpopulations derived from molecular measures. TIL densities and spatial structure were differentially enriched among tumor types, immune subtypes, and tumor molecular subtypes, implying that spatial infiltrate state could reflect particular tumor cell aberration states. Obtaining spatial lymphocytic patterns linked to the rich genomic characterization of TCGA samples demonstrates one use for the TCGA image archives with insights into the tumor-immune microenvironment

    Pan-Cancer Analysis of lncRNA Regulation Supports Their Targeting of Cancer Genes in Each Tumor Context

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    Long noncoding RNAs (lncRNAs) are commonly dys-regulated in tumors, but only a handful are known toplay pathophysiological roles in cancer. We inferredlncRNAs that dysregulate cancer pathways, onco-genes, and tumor suppressors (cancer genes) bymodeling their effects on the activity of transcriptionfactors, RNA-binding proteins, and microRNAs in5,185 TCGA tumors and 1,019 ENCODE assays.Our predictions included hundreds of candidateonco- and tumor-suppressor lncRNAs (cancerlncRNAs) whose somatic alterations account for thedysregulation of dozens of cancer genes and path-ways in each of 14 tumor contexts. To demonstrateproof of concept, we showed that perturbations tar-geting OIP5-AS1 (an inferred tumor suppressor) andTUG1 and WT1-AS (inferred onco-lncRNAs) dysre-gulated cancer genes and altered proliferation ofbreast and gynecologic cancer cells. Our analysis in-dicates that, although most lncRNAs are dysregu-lated in a tumor-specific manner, some, includingOIP5-AS1, TUG1, NEAT1, MEG3, and TSIX, synergis-tically dysregulate cancer pathways in multiple tumorcontexts

    Pan-cancer Alterations of the MYC Oncogene and Its Proximal Network across the Cancer Genome Atlas

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    Although theMYConcogene has been implicated incancer, a systematic assessment of alterations ofMYC, related transcription factors, and co-regulatoryproteins, forming the proximal MYC network (PMN),across human cancers is lacking. Using computa-tional approaches, we define genomic and proteo-mic features associated with MYC and the PMNacross the 33 cancers of The Cancer Genome Atlas.Pan-cancer, 28% of all samples had at least one ofthe MYC paralogs amplified. In contrast, the MYCantagonists MGA and MNT were the most frequentlymutated or deleted members, proposing a roleas tumor suppressors.MYCalterations were mutu-ally exclusive withPIK3CA,PTEN,APC,orBRAFalterations, suggesting that MYC is a distinct onco-genic driver. Expression analysis revealed MYC-associated pathways in tumor subtypes, such asimmune response and growth factor signaling; chro-matin, translation, and DNA replication/repair wereconserved pan-cancer. This analysis reveals insightsinto MYC biology and is a reference for biomarkersand therapeutics for cancers with alterations ofMYC or the PMN

    Interpreting breast international group (BIG) 1-98: a randomized, double-blind, phase III trial comparing letrozole and tamoxifen as adjuvant endocrine therapy for postmenopausal women with hormone receptor-positive, early breast cancer

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    The Breast International Group (BIG) 1-98 study is a four-arm trial comparing 5 years of monotherapy with tamoxifen or with letrozole or with sequences of 2 years of one followed by 3 years of the other for postmenopausal women with endocrine-responsive early invasive breast cancer. From 1998 to 2003, BIG -98 enrolled 8,010 women. The enhanced design f the trial enabled two complementary analyses of efficacy and safety. Collection of tumor specimens further enabled treatment comparisons based on tumor biology. Reports of BIG 1-98 should be interpreted in relation to each individual patient as she weighs the costs and benefits of available treatments
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