31 research outputs found

    Creating an International Learning Community

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    Thousands of university students travel to the United States every year to engage in higher education, both as undergraduates and as graduate students. This provides a strategically rich opportunity for Christian ministry that has potential for global impact. Part of this potential is to provide ministry leadership training, particularly if students are from countries that allow little freedom for such education. The challenge is to offer culturally appropriate leadership training that is applicable in various cultural contexts and that does not inadvertently cause offense by violating cultural norms of the various students. The desire is to create an educational environment that is culturally accessible to international students, and that trains domestic and international students to be leaders in our globalized world. After considering a number of approaches to address these challenges, it was decided to work with an existing local school of ministry and enable this school to transform into an International Learning Community. This dissertation and accompanying artifact provide necessary research and practical help to make such a transition possible. Section One of the dissertation describes in more detail the potential problems when working in culturally complex settings, as well as pointing out emotional and support needs unique to international students. Section Two describes several approaches considered to address the challenges. Section Three presents research that will provide substantive training content for a school staff and student body. The research focuses on cultural intelligence, cross-cultural hermeneutics, cross-cultural communication, and culture-transcending biblical leadership principles. Section Four explains the outline of x the artifact and briefly describes the courses included in the artifact. Section Five presents parameters of the artifact with brief descriptions of goals, scope, audience, and further course development indicated. Section Six discusses preliminary conclusions regarding the effectiveness of the overall project

    Benchmarking homogenization algorithms for monthly data

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    The COST (European Cooperation in Science and Technology) Action ES0601: Advances in homogenization methods of climate series: an integrated approach (HOME) has executed a blind intercomparison and validation study for monthly homogenization algorithms. Time series of monthly temperature and precipitation were evaluated because of their importance for climate studies. The algorithms were validated against a realistic benchmark dataset. Participants provided 25 separate homogenized contributions as part of the blind study as well as 22 additional solutions submitted after the details of the imposed inhomogeneities were revealed. These homogenized datasets were assessed by a number of performance metrics including i) the centered root mean square error relative to the true homogeneous values at various averaging scales, ii) the error in linear trend estimates and iii) traditional contingency skill scores. The metrics were computed both using the individual station series as well as the network average regional series. The performance of the contributions depends significantly on the error metric considered. Although relative homogenization algorithms typically improve the homogeneity of temperature data, only the best ones improve precipitation data. Moreover, state-of-the-art relative homogenization algorithms developed to work with an inhomogeneous reference are shown to perform best. The study showed that currently automatic algorithms can perform as well as manual ones

    Analysis of Clonal Type-Specific Antibody Reactions in Toxoplasma gondii Seropositive Humans from Germany by Peptide-Microarray

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    BACKGROUND: Different clonal types of Toxoplasma gondii are thought to be associated with distinct clinical manifestations of infections. Serotyping is a novel technique which may allow to determine the clonal type of T. gondii humans are infected with and to extend typing studies to larger populations which include infected but non-diseased individuals. METHODOLOGY: A peptide-microarray test for T. gondii serotyping was established with 54 previously published synthetic peptides, which mimic clonal type-specific epitopes. The test was applied to human sera (n = 174) collected from individuals with an acute T. gondii infection (n = 21), a latent T. gondii infection (n = 53) and from T. gondii-seropositive forest workers (n = 100). FINDINGS: The majority (n = 124; 71%) of all T. gondii seropositive human sera showed reactions against synthetic peptides with sequences specific for clonal type II (type II peptides). Type I and type III peptides were recognized by 42% (n = 73) or 16% (n = 28) of the human sera, respectively, while type II-III, type I-III or type I-II peptides were recognized by 49% (n = 85), 36% (n = 62) or 14% (n = 25) of the sera, respectively. Highest reaction intensities were observed with synthetic peptides mimicking type II-specific epitopes. A proportion of the sera (n = 22; 13%) showed no reaction with type-specific peptides. Individuals with acute toxoplasmosis reacted with a statistically significantly higher number of peptides as compared to individuals with latent T. gondii infection or seropositive forest workers. CONCLUSIONS: Type II-specific reactions were overrepresented and higher in intensity in the study population, which was in accord with genotyping studies on T. gondii oocysts previously conducted in the same area. There were also individuals with type I- or type III-specific reactions. Well-characterized reference sera and further specific peptide markers are needed to establish and to perform future serotyping approaches with higher resolution

    International Nonregimes: A Research Agenda1

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    Peer Reviewedhttps://deepblue.lib.umich.edu/bitstream/2027.42/146934/1/j.1468-2486.2007.00672.x.pd

    Biomarkers of a five-domain translational substrate for schizophrenia and schizoaffective psychosis

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    Abstracts from the 8th International Conference on cGMP Generators, Effectors and Therapeutic Implications

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    This work was supported by a restricted research grant of Bayer AG
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