5,215 research outputs found
Salience, Risky Choices and Gender
No full textRisk theories typically assume individuals make risky choices using probability weights that differ from objective probabilities. Recent theories suggest that probability weights vary depending on which portion of a risky environment is made salient. Using experimental data we show that salience affects young men and women differently, even after controlling for cognitive and non-cognitive skills. Men are significantly more likely than women to switch from a certain to a risky choice once the upside of winning is made salient, even though the expected value of the choice remains the same.gender, salience, risk-aversion, probability weights, cognitive ability
Unraveling TTA codon bias: Lineage-specific and positional enrichment across 11 Actinobacteria genera
No full textTransesterification in mixtures of poly(ethylene terephthalate)
No full textThe morphology of poly(ethylene terephthalate)/poly(butylene terephthalate) (PET/PBT) blends before to and after heat treatment have been studied using differential scanning calorimetry (DSC), wide and small angle x-ray scattering (WAXS and SAXS), nuclear magnetic resonance spectroscopy (NMR) and small angle neutron scattering (SANS). Blends with PET/PBT compositions of 100/0, 97/3, 90/10, 60/40, 50/50, 40/60, 25/75 and 0/100%w/w were prepared by precipitation from solutions of the two polymers at the required concentrations. Blends were heat treated to induce ester interchange reactions for a) 6 hours at 476K and b) 1/2 hour at 573K.NMR data showed that the samples iieat treated for 6 hours at 476K were block copolymers and the samples heat treated for 1/2 hour at 573K were random copolymers. DSC, WAXS and SAXS experiments established the morphology of the blends, block and random copolymers. SANS experiments were carried out to study the kinetics of transesterification of PET/PBT copolyesters. Deuterated PET has been synthesised. Data was compared for different molecular weights of deuterium-PET/hydrogenous-PBT blends prior to and after heat treatment to investigate changes in molecular weight of the deuterated chain length as a result of transesterification reactions. From these data it was possible to establish the activation energy of PBT and the results indicate that transesterification reactions take place randomly along the polymer backbone, i.e. by ester-ester interchange
Will biological agents supplant systemic glucocorticoids as the first-line treatment for thyroid-associated ophthalmopathy?
No full textIn this article, the two authors present their opposing points of view concerning the likelihood that glucocorticoids will be replaced by newly developed biological agents in the treatment of active, moderate-to-severe thyroid-associated ophthalmopathy (TAO). TAO is a vexing, disfiguring and potentially blinding autoimmune manifestation of thyroid autoimmunity. One author expresses the opinion that steroids are nonspecific, frequently fail to improve the disease and can cause sometimes serious side effects. He suggests that glucocorticoids should be replaced as soon as possible by more specific and safer drugs, once they become available. The most promising of these are biological agents. The other author argues that glucocorticoids are proven effective and are unlikely to be replaced by biologicals. He reasons that while they may not uniformly result in optimal benefit, they have been proven effective in many reports. He remains open minded about alternative therapies such as biologicals but remains skeptical that they will replace steroids as the first-line therapy for active, moderate-to-severe TAO without head-to-head comparative clinical trials demonstrating superiority. Despite these very different points of view, both authors are optimistic about the availability of improved medical therapies for TAO, either as single agents or in combination. Further, both agree that better treatment options are needed to improve the care of our patients with active moderate-to-severe TAO
The value of silence
No full textThis is an electronic version of the article published in Theatre Journal, 54(1):85-94, 2002 March. The published article is available at http://muse.jhu.edu/journals/theatre_journal/v054/54.1eng.pdfEng, David L.The Value of Silence.Theatre Journal, 54,(1):85-94, 2002.DOI: 10.1353/tj.2002.000
Design considerations and performance of a PM linear actuator in a radiation environment
No full textThis paper discusses design considerations for a water cooled high acceleration 3-phase air-cored brushless DC PM linear actuator used in a vacuum radiation environment. Radiation can cause damage to magnets, and the requirement for a vacuum chamber around the moving parts imposes additional constraints that further complicate the electromagnetic and mechanical design of the actuator. This paper discusses the selection of suitable materials and bearings that are compatible with operation in vacuum and can cope with the required millions of actuation cycles. The selection of suitable bearings with low friction and wear is discussed and the design of a low inertia shaft is described. The factors that have an influence on the susceptibility of the magnets to radiation damage are discussed. These factors include magnet dimensions, magnet material, external magnetic field, temperature and the directions of both the magnetic flux and radiation. FLUKA simulations are presented showing the fluences of protons, neutrons, electrons and gamma radiation to which the magnets are exposed. Based on these simulations, loss of magnetisation for different magnet materials can be predicted, and used to estimate the effect of magnet radiation ageing on actuator current, and increased temperature rise. The paper also presents transient electromagnet FEA computation of the force produced by the actuator when magnets are housed in a stainless steel vacuum chamber
Liftings for noncomplete probability spaces
No full textThe current state of knowledge concerning liftings for noncomplete probability spaces is discussed. This is a somewhat expanded version of the author's talk given at the 1991 Summer Conference on General Topology and Applications in Honor of Mary Ellen Rudin and Her Work.PT: S; CR: BURKE MR, IN PRESS P AM MATH S BURKE MR, 1991, ISRAEL J MATH, V73, P33 BURKE MR, 1992, ISRAEL J MATH, V79, P289 CARLSON T, THEOREM LIFTING CHRISTENSEN JPR, 1974, TOPOLOGY BOREL STRUC FREMLIN DH, 1989, HDB BOOLEAN ALGEBRAS, P877 INOESCUTULCEA A, 1966, 5TH P BERK S MATH ST, V2 IONESCUTULCEA A, 1967, CONTRIBUTIONS PROB 1, P63 IONESCUTULCEA A, 1969, TOPICS THEORY LIFTIN JECH TJ, 1978, SET THEORY JOHNSON RA, 1980, P AM MATH SOC, V80, P234 JUST W, IN PRESS T AM MATH S KUPKA J, 1983, INDIANA U MATH J, V32, P717 LOSERT V, 1983, LNM, V1080, P95 MAHARAM D, 1958, P AM MATH SOC, V9, P987 SHELAH S, 1983, ISRAEL J MATH, V45, P90 TALAGRAND M, 1982, P AM MATH SOC, V84, P379 VONNEUMANN J, 1931, CRELLES J MATH, V165, P109; NR: 18; TC: 0; J9: ANN N Y ACAD SCI; PG: 4; GA: BZ86BSource type: Electronic(1
Axisymmetric polydimethysiloxane microchannels for in vitro hemodynamic studies
No full textThe current microdevices used for biomedical research are often manufactured using microelectromechanical systems (MEMS) technology. Although it is possible to fabricate precise and reproducible rectangular microchannels using soft lithography techniques, this kind of geometry may not reflect the actual physiology of the microcirculation. Here, we present a simple method to fabricate circular polydimethysiloxane (PDMS) microchannels aiming to mimic an in vivo microvascular environment and suitable for state-of-the-art microscale flow visualization techniques, such as confocal µPIV/PTV. By using a confocal µPTV system individual red blood cells (RBCs) were successfully tracked trough a 75 µm circular PDMS microchannel. The results show that RBC lateral dispersion increases with the volume fraction of RBCs in the solution, i.e. with the hematocrit
The Imaging of a Complete Biological Structure with the Scanning Tunneling Microscope
No full textPT: J; CR: 1986, IBM J RES DEV, V30 AMREIN M, 1988, IN PRESS J MICROSCOP AMREIN M, 1988, SCIENCE, V240, P514 BEVERIDGE TJ, 1985, J BACTERIOL, V162, P728 BEVERIDGE TJ, 1987, CAN J MICROBIOL, V33, P725 BINNIG G, 1982, HELV PHYS ACTA, V55, P726 BLACKFORD BL, 1987, REV SCI INSTRUM, V58, P1343 BLACKFORD BL, 1988, IN PRESS J MICROSCOP DAHN DC, 1988, J VAC SCI TECHNOL A, V6, P548 FOSTER JS, 1988, IN PRESS J MICROSCOP HANSMA PK, 1987, J APPL PHYS, V61, R1 LINDSAY SM, 1988, J VAC SCI TECHNOL A, V6, P544 SHAW PJ, 1985, J BACTERIOL M, V161, P650 SMITH D, 1988, IN PRESS J MICROSCOP SMITH DPE, 1987, P NATL ACAD SCI USA, V84, P969 SONNENFELD R, 1986, SCIENCE, V232, P211 SPROTT GD, 1980, CAN J MICROBIOL, V26, P115 SPROTT GD, 1986, CAN J MICROBIOL, V32, P847 STEMMER A, 1987, SURF SCI, V181, P394 STEWART M, 1985, J MOL BIOL, V183, P509 STROSCIO JA, 1987, PHYS REV LETT, V58, P1668 ZASADZINSKI JAN, 1988, SCIENCE, V239, P1013; NR: 22; TC: 12; J9: ULTRAMICROSCOPY; PG: 6; GA: AA937Source type: Electronic(1
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