22 research outputs found

    Improving Qualifying Exam Performance—From Assessment Data to Curriculum Alignment

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    This poster describes the effort of the Ph.D. Committee in Social Welfare in investigating and improving students’ performance in the qualifying exam. Motivated by an analysis of students’ (cohorts Fall 2010 – 2014) pass rate, faculty reviewed the exam questions, analyzed the course syllabi and exam questions. The committee changed the exam timeline and revised the exam questions so that the exam better reflected the curriculum

    Articulating social welfare PhD program rubrics toward sustainable assessment

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    The Myron B. Thompson School of Social Work (SW) PhD program at the University of Hawaiʻi at Mānoa currently has 16 students and 10 graduate faculty members. Developing and implementing sustainable PhD assessment plans are necessary to reflect student learning and curriculum improvements. Articulating the PhD program rubrics into a program-level assessment plan is imperative. The SW PhD program has developed seven Student Learning Outcomes (SLOs), assessable outcomes, and a curriculum map. In Fall of 2015, the PhD program committee revisited the SLOs and made revisions in alignment with the sustainable assessment plan for the program as a foundational step for creating program rubrics. The committee developed program rubrics for benchmarks—(a) specialization, (b) comprehensive examination (i.e., dissertation proposal), and (c) final exam (i.e., dissertation defense)—that are tied to the SLOs. The committee began collecting data using developed rubrics in Spring 2016 as a pilot to gain additional clarity on the rubrics in order to make them efficient and manageable as key parts of PhD program curriculum. During the process of developing the rubrics, the PhD committee collaborated to facilitate the assessment planning process. During this assessment process, the committee has utilized existing materials and sources, such as student products (e.g., dissertation proposal), evaluation criteria (e.g., dissertation evaluation), yearly advising sessions, and student reviews materials. This poster presents the strategies utilized in the pilot project as well as lessons learned through the project

    An external quality assessment feasibility study; cross laboratory comparison of haemagglutination inhibition assay and microneutralization assay performance for seasonal influenza serology testing: A FLUCOP study

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    Introduction: External Quality Assessment (EQA) schemes are designed to provide a snapshot of laboratory proficiency, identifying issues and providing feedback to improve laboratory performance and inter-laboratory agreement in testing. Currently there are no international EQA schemes for seasonal influenza serology testing. Here we present a feasibility study for conducting an EQA scheme for influenza serology methods. Methods: We invited participant laboratories from industry, contract research organizations (CROs), academia and public health institutions who regularly conduct hemagglutination inhibition (HAI) and microneutralization (MN) assays and have an interest in serology standardization. In total 16 laboratories returned data including 19 data sets for HAI assays and 9 data sets for MN assays. Results: Within run analysis demonstrated good laboratory performance for HAI, with intrinsically higher levels of intra-assay variation for MN assays. Between run analysis showed laboratory and strain specific issues, particularly with B strains for HAI, whilst MN testing was consistently good across labs and strains. Inter-laboratory variability was higher for MN assays than HAI, however both assays showed a significant reduction in inter-laboratory variation when a human sera pool is used as a standard for normalization. Discussion: This study has received positive feedback from participants, highlighting the benefit such an EQA scheme would have on improving laboratory performance, reducing inter laboratory variation and raising awareness of both harmonized protocol use and the benefit of biological standards for seasonal influenza serology testing.publishedVersio

    Nanotools for Neuroscience and Brain Activity Mapping

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    Neuroscience is at a crossroads. Great effort is being invested into deciphering specific neural interactions and circuits. At the same time, there exist few general theories or principles that explain brain function. We attribute this disparity, in part, to limitations in current methodologies. Traditional neurophysiological approaches record the activities of one neuron or a few neurons at a time. Neurochemical approaches focus on single neurotransmitters. Yet, there is an increasing realization that neural circuits operate at emergent levels, where the interactions between hundreds or thousands of neurons, utilizing multiple chemical transmitters, generate functional states. Brains function at the nanoscale, so tools to study brains must ultimately operate at this scale, as well. Nanoscience and nanotechnology are poised to provide a rich toolkit of novel methods to explore brain function by enabling simultaneous measurement and manipulation of activity of thousands or even millions of neurons. We and others refer to this goal as the Brain Activity Mapping Project. In this Nano Focus, we discuss how recent developments in nanoscale analysis tools and in the design and synthesis of nanomaterials have generated optical, electrical, and chemical methods that can readily be adapted for use in neuroscience. These approaches represent exciting areas of technical development and research. Moreover, unique opportunities exist for nanoscientists, nanotechnologists, and other physical scientists and engineers to contribute to tackling the challenging problems involved in understanding the fundamentals of brain function

    Intestinal uptake of lipovitellin from brine shrimp (Artemia franciscana) by larval inland silversides (Menidia beryllina) and striped bass (Morone saxatilis)

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    Intestinal uptake of lipovitellin (LV) from brine shrimp (Artemia franciscana) in larval inland silversides (Menidida beryllina) and striped bass (Morone saxatilis) was described using immunocytochemistry. Polyclonal antisera were raised against two subunits of LV (LV68 and LV190). When tested by immunocytochemistry, anti-LV68 showed cross-reactivity with some of the pancreatic cells especially in inland silversides. Therefore anti-LV190 was used to localize immunoreactive LV. Inland silversides at 14 days after hatching were fed Artemia nauplii and then sampled 4, 8, 12 hr after feeding. Similar experiments were carried out by using striped bass at 5 days and 15 days of age. They were sampled at 2, 4, 8, and 12 hr after feeding. Anterior enterocytes showed no evidence of uptake; however, the brush border of the cells of inland silversides reacted with the antiserum. Posterior enterocytes took up the LV and/or, possibly, their immunoreactive breakdown products. The pattern of uptake included accumulation in supranuclear vacuoles and digestion in supranuclear vacuoles, as suggested by the decay of the immunoreactivity over time. Thus, the posterior intestine of these larval fishes is the site of uptake and digestion of LV, an important nutritive component in the food of many larval fishes; this supports earlier findings using non-nutritive marker proteins

    Some determinants of morphology and release rate from poly()lactic acid microspheres

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    Morphology and release rate from poly()lactic acid microspheres were studied as a function of drug loading, drug lipophilicity and solvent evaporation rate. Sudan III was used to exemplify lipophilic compounds, while etoposide served as a relatively polar drug. Drug loading was found to be an important determinant of morphology, with increased formation of distorted microspheres at higher loadings. In the case of the polar etoposide, this translated into a greater release rate. For Sudan III, however, negligible release occurred despite morphological changes, suggesting that the drug lipophilicity is also important as a determinant of release rate. When gelatin was used as the emulsifying agent, the percentage of distorted microspheres and the release rate were highly dependent on the rate of solvent evaporation. When smooth microspheres were produced with polyvinyl alcohol as the emulsifying agent, drying rate was found to be of less importance.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/28487/1/0000281.pd

    Liquifaction at Strong Motion Stations and in Urayasu City during the 2011 Tohoku-Oki Earthquake

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    The 2011 MW = 9.0 Tohoku-oki earthquake generated a large number of unique soil liquefaction case histories, including cases with strong ground motion recordings on liquefiable or potentially liquefiable soils. We have compiled a list of 22 strong motion stations (SMS) where surface evidence of liquefaction was observed and 16 SMS underlain by geologically recent sediments or fills where surface evidence of liquefaction was not observed. Pre-earthquake standard penetration test data and borehole shear wave velocity (Vs) profiles are available for some stations, but critical information, such as grain size distribution and fines plasticity, are often lacking. In the heavily damaged city of Urayasu, we performed post-earthquake cone penetration testing at seven SMS and Vs profiles, using surface wave methods at 28 additional locations to supplement existing geotechnical data. We describe the liquefaction effects in Urayasu, the available site characterization data, and our initial data interpretations

    ÎČ-Catenin stabilization stalls the transition from double-positive to single-positive stage and predisposes thymocytes to malignant transformation

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    Activation of ÎČ-catenin has been causatively linked to the etiology of colon cancer. Conditional stabilization of this molecule in pro-T cells promotes thymocyte development without the requirement for pre-TCR signaling. We show here that activated ÎČ-catenin stalls the developmental transition from the double-positive (DP) to the single-positive (SP) thymocyte stage and predisposes DP thymocytes to transformation. ÎČ-Catenin–induced thymic lymphomas have a leukemic arrest at the early DP stage. Lymphomagenesis requires Rag activity, which peaks at this developmental stage, as well as additional secondary genetic events. A consistent secondary event is the transcriptional up-regulation of c-Myc, whose activity is required for transformation because its conditional ablation abrogates lymphomagenesis. In contrast, the expression of Notch receptors as well as targets is reduced in DP thymocytes with stabilized ÎČ-catenin and remains low in the lymphomas, indicating that Notch activation is not required or selected for in ÎČ-catenin–induced lymphomas. Thus, ÎČ-catenin activation may provide a mechanism for the induction of T-cell–acute lymphoblastic leukemia (T-ALL) that does not depend on Notch activation
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