9 research outputs found

    INTERDISCIPLINARY VARIATIONS IN THE PERCEPTION OF POWER: A STUDY IN IDEOLOGY

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    There have been marked disagreements in the literature on the structure of power in American society. The authors suggest that this controversy is an artifact of ideological differences between sociologists and political scientists. This hypothesis is tested through the use of a pluralism-elitism scale. Political scientists are found to score toward the pluralistic end of the spectrum, while sociologists are concentrated toward the elitist end, thus providing preliminary support for the hypothesis

    The state of the science and vision of the future: Report from the Hydrogeophysics Workshop

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    peer reviewedIn July 2012, 72 hydrogeophysicists from around the world gathered at the Hydrogeophysics Workshop in Boise, Idaho, USA. This was the first workshop to be jointly sponsored by the Society of Exploration Geophysicists (SEG) and the American Geophysical Union (AGU), and brought together members from both societies, primarily from the Near-Surface Geophysics Section of SEG and the Near-Surface Focus Group and Hydrology Section of AGU. The intent of the workshop was to address current hydrogeophysical approaches for determining, predicting, and studying hydrologic properties and processes in both the saturated and unsaturated zones, at scales ranging from centimeters to watersheds

    A decade of genome-wide gene expression profiling in acute myeloid leukemia: flashback and prospects

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    The past decade has shown a marked increase in the use of high-throughput assays in clinical research into human cancer, including acute myeloid leukemia (AML). In particular, genome-wide gene expression profiling (GEP) using DNA microarrays has been extensively used for improved understanding of the diagnosis, prognosis, and pathobiology of this heterogeneous disease. This review discusses the progress that has been made, places the technologic limitations in perspective, and highlights promising future avenue

    The Streamlined Sales and Use Tax Agreement: A California Perspective

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    Empagliflozin in Patients with Chronic Kidney Disease

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    Background The effects of empagliflozin in patients with chronic kidney disease who are at risk for disease progression are not well understood. The EMPA-KIDNEY trial was designed to assess the effects of treatment with empagliflozin in a broad range of such patients. Methods We enrolled patients with chronic kidney disease who had an estimated glomerular filtration rate (eGFR) of at least 20 but less than 45 ml per minute per 1.73 m(2) of body-surface area, or who had an eGFR of at least 45 but less than 90 ml per minute per 1.73 m(2) with a urinary albumin-to-creatinine ratio (with albumin measured in milligrams and creatinine measured in grams) of at least 200. Patients were randomly assigned to receive empagliflozin (10 mg once daily) or matching placebo. The primary outcome was a composite of progression of kidney disease (defined as end-stage kidney disease, a sustained decrease in eGFR to < 10 ml per minute per 1.73 m(2), a sustained decrease in eGFR of & GE;40% from baseline, or death from renal causes) or death from cardiovascular causes. Results A total of 6609 patients underwent randomization. During a median of 2.0 years of follow-up, progression of kidney disease or death from cardiovascular causes occurred in 432 of 3304 patients (13.1%) in the empagliflozin group and in 558 of 3305 patients (16.9%) in the placebo group (hazard ratio, 0.72; 95% confidence interval [CI], 0.64 to 0.82; P < 0.001). Results were consistent among patients with or without diabetes and across subgroups defined according to eGFR ranges. The rate of hospitalization from any cause was lower in the empagliflozin group than in the placebo group (hazard ratio, 0.86; 95% CI, 0.78 to 0.95; P=0.003), but there were no significant between-group differences with respect to the composite outcome of hospitalization for heart failure or death from cardiovascular causes (which occurred in 4.0% in the empagliflozin group and 4.6% in the placebo group) or death from any cause (in 4.5% and 5.1%, respectively). The rates of serious adverse events were similar in the two groups. Conclusions Among a wide range of patients with chronic kidney disease who were at risk for disease progression, empagliflozin therapy led to a lower risk of progression of kidney disease or death from cardiovascular causes than placebo
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