274 research outputs found

    Leistungstest, Offenheit von Bildungsgängen und obligatorische Beratung der Eltern: Reduziert das Deutschfreiburger Übergangsmodell die Effekte des sozialen Hintergrunds bei Übergangsentscheidungen?

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    Dieser Beitrag untersucht das Übertrittsverfahren von der Grundschule in die Sekundarschule I der deutschsprachigen Schulen des Kantons Freiburg (Schweiz). Das Deutschfreiburger Übergangsmodell mit seinen verschiedenen Komponenten wird vorgestellt und evaluiert. Ein besonderes Augenmerk liegt dabei auf der Frage, ob unerwünschte Effekte des familiären Hintergrunds durch dieses Modell reduziert bzw. eliminiert werden können. Untersucht wird im Weiteren die Übereinstimmung der Übertrittsempfehlung von Eltern und Lehrkräften sowie der Prüfungsleistung. Die Autoren kommen zum Schluss, dass das untersuchte Übergangsmodell die Effekte des familiären Hintergrunds beim Übertritt von der Primarschule in die Sekundarschule relativ gering hält. Der sozioökonomische Hintergrund wirkt sich über die Übertrittsempfehlung von Lehrkräften und Eltern auch auf den tatsächlichen Übertritt aus; die absoluten Effekte des familiären Hintergrunds fallen jedoch – nach Kontrolle der Schulleistung – insgesamt vergleichsweise schwach aus. Der eingesetzte Bewertungsbogen, den Lehrkräfte und Eltern zusätzlich zu den Noten als Basis fürm die Übergangsempfehlung einsetzen, scheint resistent gegenüber Effekten des familiären Hintergrunds zu sein

    Positive selection at codon 38 of the human KCNE1 (= minK) gene and sporadic absence of 38Ser-coding mRNAs in Gly38Ser heterozygotes

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    <p>Abstract</p> <p>Background</p> <p>KCNE1 represents the regulatory beta-subunit of the slowly activating delayed rectifier potassium channel (IKs). Variants of KCNE1 have repeatedly been linked to the long-QT syndrome (LQTS), a disorder which predisposes to deafness, ventricular tachyarrhythmia, syncope, and sudden cardiac death.</p> <p>Results</p> <p>We here analyze the evolution of the common Gly38Ser variant (rs1805127), using genomic DNAs, complementary DNAs, and HEK293-expressed variants of altogether 19 mammalian species. The between species comparison reveals that the human-specific Gly38Ser polymorphism evolved under strong positive Darwinian selection, probably in adaptation to specific challenges in the fine-tuning of IKs channels. The involved amino acid exchanges (Asp > Gly, Gly > Ser) are moderately radical and do not induce apparent changes in posttranslational modification. According to population genetic analyses (HapMap phase II) a heterozygote advantage accounts for the maintenance of the Gly38Ser polymorphism in humans. On the other hand, the expression of the 38Ser allele seems to be disadvantageous under certain conditions, as suggested by the sporadic deficiency of 38Ser-coding mRNAs in heterozygote Central Europeans and the depletion of homozygotes 38Ser in the Yoruban sample.</p> <p>Conclusion</p> <p>We speculate that individual differences in genomic imprinting or genomic recoding might have contributed to conflicting results of recent association studies between Gly38Ser polymorphism and QT phenotype. The findings thus highlight the relevance of mRNA data in future association studies of genotypes and clinical disorders. To the best of our knowledge, they moreover provide first time evidence for a unique pattern; i.e. coincidence of positive Darwinian selection and polymorphism with a sporadically suppressed expression of one allele.</p

    A profile shape correction to reduce the vertical sensitivity of cosmic-ray neutron sensing of soil moisture

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    n recent years, cosmic-ray neutron sensing (CRNS) has shown a large potential among proximal sensing techniques to monitor soil moisture noninvasively, with high frequency and a large support volume (radius up to 240 m and sensing depth up to 80 cm). This signal is, however, more sensitive to closer distances and shallower depths. Inherently, CRNS-derived soil moisture is a spatially weighted value, different from an average soil moisture as retrieved by a sensor network. In this study, we systematically test a new profile shape correction on CRNS-derived soil moisture, based on additional soil moisture profile measurements and vertical unweighting, which is especially relevant during pronounced wetting or drying fronts. The analyses are conducted with data collected at four contrasting field sites, each equipped with a CRNS probe and a distributed soil moisture sensor network. After applying the profile shape correction on CRNS-derived soil moisture, it is compared with the sensor network average. Results show that the influence of the vertical sensitivity of CRNS on integral soil moisture values is successfully reduced. One to three properly located profile measurements within the CRNS support volume improve the performance. For the four investigated field sites, the RMSE decreased 11–53% when only one profile location was considered. We therefore recommend to install along with a CRNS at least one soil moisture profile in a radial distanceProfile-shape-corrected, CRNS-derived soil moisture is an unweighted integral soil moisture over the support volume, which is easier to interpret and easier to use for further applications

    Excursions into suburban density

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    Non peer reviewe

    Memorial Service for Werner Seligmann: Distiguished Professor of Architecture

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    Memorial Service for Werner Seligmann (1930-1998) was held in Hendricks Chapel, Syracuse University on December 6th, 1998 at 1:30pm

    Heterodimerization of AML1/ETO with CBFβ is required for leukemogenesis but not for myeloproliferation

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    The AML1/Runx1 transcription factor and its heterodimerization partner CBFβ are essential regulators of myeloid differentiation. The chromosomal translocation t(8;21), fusing the DNA binding domain of AML1 to the corepressor eight-twenty-one (ETO), is frequently associated with acute myeloid leukemia and generates the AML1/ETO (AE) fusion protein. AE represses target genes usually activated by AML1 and also affects the endogenous repressive function of ETO at Notch target genes. In order to analyze the contribution of CBFβ in AE-mediated leukemogenesis and deregulation of Notch target genes, we introduced two point mutations in a leukemia-initiating version of AE in mice, called AE9a, that disrupt the AML1/CBFβ interaction (AE9aNT). We report that the AE9a/CBFβ interaction is not required for the AE9a-mediated aberrant expression of AML1 target genes, while upregulation/derepression of Notch target genes does require the interaction with CBFβ. Using retroviral transduction to express AE9a in murine adult bone marrow-derived hematopoietic progenitors, we observed that both AE9a and AE9aNT lead to increased myeloproliferation in vivo. However, both development of leukemia and long-term replating capacity are only observed with AE9a but not with AE9aNT. Thus, deregulation of both AML1 and Notch target genes is required for the development of AE9a-driven leukemia
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