630 research outputs found

    The Ursinus Weekly, May 6, 1963

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    Report submitted by 1963-64 Women\u27s Customs Committee • Proctors named for coming year • Fred Yocum and Dr. Zucker to represent UC in June Y conference • Debating Club to present mock College Bowl • Douglas Steere to speak in expanded Forum Wednesday • Sophs & new frosh receive required Summer reading • Spring Festival weekend May 10-11; The staring match begins activities • Dr. Wagner plied by students in 3rd Controversy • Bob Larzelere elected to head Men\u27s Customs next year • Tibetan lamas to visit Ursinus • Letters to the editor • It\u27s all over • Greek gleanings • Whistlestops final step in Spring rushing • Pre-med society hears Dr. Cochran • Mike Bernstein receives honors • Nominations made for class officers • UC Band concert scheduled May 11 • Pre-med elections this week • Cheerleaders name squad members • Meistersingers performance superb • WSGA meeting • Bears out-poll Diplomats 10-4; Deep-freeze, rain dissolve E-Town • Wilkes stuns UC\u27s chances 2-1 • UC downs WC in lacrosse, 10-4 • Netmen conquer Drexel and PMC • Favored Drexel smashed by UC golf club • Cindermen raise season record 6-1 • Haverford defeats UC golf teamhttps://digitalcommons.ursinus.edu/weekly/1295/thumbnail.jp

    Circadian Activity of Topical 0.05% Betamethasone Dipropionate in Human Skin In Vivo

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    The influence of treatment duration, vehicle, and time of day of application on topical 0.05% betamethasone dipropionate uptake into human stratum corneum and the resulting skin- blanching response was investigated in human subjects. Drug uptake into stratum corneum and the resulting skin color changes measured with a chromameter demonstrate an equilibrium delay. Maximal drug uptake occurred at 2 h, whereas maximal skin color changes occurred 6h after a single application. Extent of decreased skin color was dependent on vehicle, treatment duration, and time of day of application. Time of maximal decreased skin color occurred at midnight independent of vehicle, treatment duration, or time of day of application. This time of maximal drug activity coincides with the well-known time period of lowest circulating cortisol concentrations (2000-0400 h). Application of a single 2- or 6-h dose of the 0.05% cream at 1600h produced more extensive and prolonged changes in skin color over 24h than a 0900-h application in the same subject. These data demonstrate that the extent and duration of topical corticosteroid activity in human skin is influenced by vehicle, treatment duration, and time of day of application. The prolonged changes in skin color measured with a single dose applied at 1600h suggest that a once-a-day dosing regimen in the late afternoon may be sufficient for dermatologic therapy. Elucidation of these circadian responses with topical corticosteroids may provide a rational basis for the future re-evaluation of the appropriate therapeutic regimen with this class of drugs in dermatologic medicine

    The Ursinus Weekly, November 11, 1963

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    Carol Heber, Homecoming queen; Emmert receives Walker trophy • Catherine Drinker Bowen to be guest speaker at Forum • WSGA meeting set for Sunday • Past UC speaker in protest against Mme. Nhu before fall of regime • Volunteers for St. Gabriels to meet Tuesday • Alumni contribute $220,000 to Centennial Fund • Student rumor clarified • 17 men go Greek in Fall rushing • AAUW discusses community college • Professor chief editor of new publication • Ursinus gets portrait of Henry T. Spangler • Folksing begins weekend • MSGA sponsors bus to next game • Editorial: Women, it\u27s now or never; Kaffee Klatsch; Complaint for complaint\u27s sake? • Have you read: Travels with Charley • Swedish student studying here • Art class tours Philly museum • Letters to the editor • Excellent concert heard by students • Colgan views Cuba as potential source of war • Republicans view election returns • Thai student to speak at Kaffee Klatsch Friday • Ursinus Band: Review & outlook • Greek gleanings • Senior women reply to WSGA questionnaire with emphatic views • Jobs open for political interns • Parsons speaks on Daniel Claus • Outing Club on spelunking trip • Alpha Phi Omega plans open meeting • Bears trounce Fords 32 to 8 as Emmert stars in Homecoming tilt • Player of the week interview: Ron Emmert • UC puts three on college team • Soccer team beats La Salle, alumni • JV and 3rd teams take Immaculatahttps://digitalcommons.ursinus.edu/weekly/1257/thumbnail.jp

    From Process to Product: Your Risk Process at Work

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    The Space Life Sciences Directorate (SLSD) and Human Research Program (HRP) at the NASA/Johnson Space Center work together to address and manage the human health and performance risks associated with human space flight. This includes all human system requirements before, during, and after space flight, providing for research, and managing the risk of adverse long-term health outcomes for the crew. We previously described the framework and processes developed for identifying and managing these human system risks. The focus of this panel is to demonstrate how the implementation of the framework and associated processes has provided guidance in the management and communication of human system risks. The risks of early onset osteoporosis, CO2 exposure, and intracranial hypertension in particular have all benefitted from the processes developed for human system risk management. Moreover, we are continuing to develop capabilities, particularly in the area of information architecture, which will also be described. We are working to create a system whereby all risks and associated actions can be tracked and related to one another electronically. Such a system will enhance the management and communication capabilities for the human system risks, thereby increasing the benefit to researchers and flight surgeons

    Differential Gene Expression Profiling of Orbital Adipose Tissue in Thyroid Orbitopathy

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    Published under a Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/legalcode)PURPOSE. We aimed to determine differentially expressed genes relevant to orbital inflammation and orbital fat expansion in thyroid orbitopathy (TO) using microarray gene profiling in a case-control study. METHODS. Human orbital adipose samples were obtained from individuals with active TO (n ¼ 12), inactive TO (n ¼ 21), and normal controls (n ¼ 21). Gene expression profiles were examined using microarray analysis and were compared between active and inactive TO, and between active TO and normal controls. Top ranked differentially expressed genes were validated by real-time RT-PCR in an additional eight active TO, 13 inactive TO, and 11 normal controls and correlated with gene set enrichment analysis (GSEA) and molecular pathways analysis. RESULTS. Seven hundred twenty-one probes (683 genes) and 806 probes (735 genes) were significantly differentially expressed in comparing active to inactive TO and in comparing active TO to healthy controls, respectively. All selected genes were confirmed to be differentially expressed by real-time RT-PCR. Multiple top ranked genes in active versus inactive TO comparison are overrepresented by immune and inflammatory response genes. They include defensins (DEFA1, DEFA1B, DEFA3), which were overexpressed by 3.05- to 4.14-fold and TIMD4 by 4.20-fold. Markers for adipogenesis were overexpressed including SCD, FADS1, and SCDP1. Gene set enrichment analysis revealed dysregulation of epigenetic signatures, T-cell activation, Th1 differentiation, defensin pathway, cell adhesion, cytoskeleton organization, apoptosis, cell cycling, and lipid metabolism in active TO. CONCLUSIONS. Active TO is characterized by upregulation of genes involved in cell-mediated immune, innate immune, and inflammatory response and enhanced orbital adipogenesis. TIMD4, DEFA1, DEFA1B, and DEFA3 genes may be involved in the innate immune-mediated orbital inflammation in TO. Epigenetic mechanisms may play a role in the pathogenesis of TO
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