TY - THES A1 - Bachsleitner, Anna T1 - Bildungsverläufe und soziale Ungleichheit vom Abitur bis zur Promotion N2 - Übergänge im Bildungssystem sind zentrale Stationen für die Generierung von sozialer Ungleichheit. Während die Bildungswege und die Bedeutung der sozialen Ungleichheit für den Schulbereich umfangreich untersucht wurden, liegen kaum Studien zu den nachschulischen Bildungsverläufen von Hochschulzugangsberechtigten und dem Einfluss der sozialen Herkunft bis zur Aufnahme einer Promotion vor. Daher ist es das Ziel der vorliegenden Arbeit, die Gestaltung nachschulischer Bildungsverläufe zu untersuchen sowie die Bedeutung der sozialen Herkunft vom Abitur bis zur Promotionsaufnahme zu analysieren. Den beiden Forschungsfragen wurde in vier Teilstudien nachgegangen. In Teilstudie 1 wurde die Relevanz von Merkmalen des Bildungsverlaufes für die Promotionsaufnahme untersucht. Der Schwerpunkt der drei folgenden Teilstudien lag auf der Bedeutung der sozialen Herkunft bei Aufnahme einer Promotion beziehungsweise der sozialen Ungleichheit in den relevanten Selektionsstufen des nachschulischen Bildungsverlaufs bis zur Promotionsaufnahme. In Teilstudie 2 wurden diesbezüglich soziale Herkunftseffekte bei der für eine Promotionsaufnahme bedeutsamen Wahl der Hochschulform untersucht, in Teilstudie 3 die Mechanismen hinter sozialen Herkunftseffekten bei Promotionsaufnahme analysiert und in Teilstudie 4 wurde soziale Ungleichheit bei Studienaufnahme und Promotionsaufnahme vergleichend betrachtet. Als Datengrundlage wurde die Längsschnittstudie BIJU (Bildungsverläufe und psychosoziale Entwicklung im Jugend- und jungen Erwachsenenalter) herangezogen. Die Befunde der Dissertation verweisen auf die Relevanz sozialer Ungleichheiten vom Eintritt in die Hochschule bis zum Übergang in die Promotion. Auch wenn ein abnehmender Herkunftseffekt vom Übertritt ins Studium zum Übertritt in die Promotion vorliegt, sind soziale Herkunftseffekte bei dem späten Bildungsübergang noch sichtbar. Zudem zeigt sich die Bedeutung von Pfadabhängigkeiten in Bildungsverläufen sowie von Leistungsunterschieden für eine Promotionsaufnahme. KW - Bildungsverlauf KW - soziale Ungleichheit KW - Bildungsübergänge KW - tertiäre Bildung KW - Promotionsaufnahme Y1 - 2019 ER - TY - JOUR A1 - Maluch, Jessica Tsimprea A1 - Kempert, Sebastian Benjamin T1 - Bilingual profiles and third language learning: the effects of the manner of learning, sequence of bilingual acquisition, and language use practices JF - International Journal of Bilingual Education and Bilingualism N2 - This study investigates the effect of bilingualism on learning English as a foreign language (L3), examining the impact of manner and sequence of bilingual acquisition and learning as well as language use practices in language minority children. With a sample of 1295 German eighth and ninth graders (bilingual: n = 456, monolingual: n = 839), we examined if certain aspects of bilingualism present an advantageous condition for learning English as a foreign language in bilingual language minority students. Controlling for socio-economic status, indicators of cultural capital, and gender, the regression analyses revealed higher L3 listening and reading outcomes for bilinguals who received formal instruction in their minority language, had acquired both languages in their first three years, and switched more often between their two languages, when compared to their other bilingual and monolingual peers. The discussion focuses on the importance for bilingual children in immigrant communities to have high proficiencies in both majority and minority languages in order to develop advantages in foreign language learning. KW - Bilingualism KW - language minority learners KW - foreign language learning KW - multilingualism KW - third language acquisition Y1 - 2019 U6 - https://doi.org/10.1080/13670050.2017.1322036 SN - 1367-0050 SN - 1747-7522 VL - 22 IS - 7 SP - 870 EP - 882 PB - Routledge, Taylor & Francis Group CY - Abingdon ER - TY - JOUR A1 - Sass, Stephan A1 - Stöcklein, Walter F. M. A1 - Klevesath, Anja A1 - Hurpin, Jeanne A1 - Menger, Marcus A1 - Hille, Carsten T1 - Binding affinity data of DNA aptamers for therapeutic anthracyclines from microscale thermophoresis and surface plasmon resonance spectroscopy JF - The analyst : the analytical journal of the Royal Society of Chemistry N2 - Anthracyclines like daunorubicin (DRN) and doxorubicin (DOX) play an undisputed key role in cancer treatment, but their chronic administration can cause severe side effects. For precise anthracycline analytical systems, aptamers are preferable recognition elements. Here, we describe the detailed characterisation of a single-stranded DNA aptamer DRN-10 and its truncated versions for DOX and DRN detection. Binding affinities were determined from surface plasmon resonance (SPR) and microscale thermophoresis (MST) and combined with conformational data from circular dichroism (CD). Both aptamers displayed similar nanomolar binding affinities to DRN and DOX, even though their rate constants differed as shown by SPR recordings. SPR kinetic data unravelled a two-state reaction model including a 1 : 1 binding and a subsequent conformational change of the binding complex. This model was supported by CD spectra. In addition, the dissociation constants determined with MST were always lower than that from SPR, and especially for the truncated aptamer they differed by two orders of magnitude. This most probably reflects the methodological difference, namely labelling for MST vs. immobilisation for SPR. From CD recordings, we suggested a specific G-quadruplex as structural basis for anthracycline binding. We concluded that the aptamer DRN-10 is a promising recognition element for anthracycline detection systems and further selected aptamers can be also characterised with the combined methodological approach presented here. Y1 - 2019 U6 - https://doi.org/10.1039/c9an01247h SN - 0003-2654 SN - 1364-5528 VL - 144 IS - 20 SP - 6064 EP - 6073 PB - Royal Society of Chemistry CY - Cambridge ER - TY - THES A1 - Jennek, Julia T1 - Binnendifferenzierung in der Sekundarstufe I BT - eine quantitative Videoanalyse Y1 - 2019 ER - TY - JOUR A1 - Jetzschmann, Katharina J. A1 - Tank, Steffen A1 - Jagerszki, Gyula A1 - Gyurcsanyi, Robert E. A1 - Wollenberger, Ulla A1 - Scheller, Frieder W. T1 - Bio-Electrosynthesis of Vectorially Imprinted Polymer Nanofilms for Cytochrome P450cam JF - ChemElectroChem N2 - A new approach for synthesizing a vectorially imprinted polymer (VIP) is presented for the microbial cytochrome P450cam enzyme. A surface attached binding motif of a natural reaction partner of the target protein, putidaredoxin (Pdx), is the anchor to the underlying transducer. The 15 amino acid peptide anchor, which stems from the largest continuous amino acid chain within the binding site of Pdx was modified: (i) internal cysteines were replaced by serines to prevent disulfide bond formation; (ii) 2 ethylene glycol units were attached to the N-terminus as a spacer region; and (iii) an N-terminal cysteine was added to allow the immobilization on the gold electrode surface. Immobilization on GCE was achieved via an N-(1-pyrenyl)maleimide (NPM) cross-linker. In this way oriented immobilization of P450cam was accomplished by binding it to a peptide-modified gold or glassy carbon electrode (GCE) prior to the electrosynthesis of a polymer nanofilm around the immobilized target. This VIP nanofilm enabled reversible oriented docking of P450cam as it is indicated by the catalytic oxygen reduction via direct electron transfer between the enzyme and the underlying electrode. Catalysis of oxygen reduction by P450cam bound to the VIP-modified GCE was used to measure rebinding to the VIP. The mild coupling of an oxidoreductase with the electrode may be appropriate for realizing electrode-driven substrate conversion by instable P450 enzymes without the need of NADPH co-factor. KW - cytochrome P450 KW - direct electron transfer KW - electropolymerization KW - molecularly imprinted polymers KW - protein imprinting Y1 - 2019 U6 - https://doi.org/10.1002/celc.201801851 SN - 2196-0216 VL - 6 IS - 6 SP - 1818 EP - 1823 PB - Wiley-VCH CY - Weinheim ER - TY - CHAP A1 - Schlaad, Helmut A1 - Luedecke, Nils T1 - Bio-sourced chelating poly(2-oxazoline)s T2 - Abstracts of papers : joint conference / The Chemical Institute of Cananda, CIC, American Chemical Society, ACS Y1 - 2019 SN - 0065-7727 VL - 257 PB - American Chemical Society CY - Washington ER - TY - JOUR A1 - Reinicke, Stefan A1 - Fischer, Thilo A1 - Bramski, Julia A1 - Pietruszka, Jörg A1 - Böker, Alexander T1 - Biocatalytically active microgels by precipitation polymerization of N-isopropyl acrylamide in the presence of an enzyme JF - RSC Advances N2 - We present a novel protocol for the synthesis of enzymatically active microgels. The protocol is based on the precipitation polymerization of N-isopropylacrylamide (NIPAm) in the presence of an enzyme and a protein binding comonomer. A basic investigation on the influence of different reaction parameters such as monomer concentration and reaction temperature on the microgel size and size distribution is performed and immobilization yields are determined. Microgels exhibiting hydrodynamic diameters between 100 nm and 1 mu m and narrow size distribution could be synthesized while about 31-44% of the enzyme present in the initial reaction mixture can be immobilized. Successful immobilization including a verification of enzymatic activity of the microgels is achieved for glucose oxidase (GOx) and 2-deoxy-d-ribose-5-phosphate aldolase (DERA). The thermoresponsive properties of the microgels are assessed and discussed in the light of activity evolution with temperature. The positive correlation of enzymatic activity with temperature for the GOx containing microgel originates from a direct interaction of the enzyme with the PNIPAm based polymer matrix whose magnitude is highly influenced by temperature. Y1 - 2019 U6 - https://doi.org/10.1039/c9ra04000e SN - 2046-2069 VL - 9 IS - 49 SP - 28377 EP - 28386 PB - Royal Society of Chemistry CY - Cambridge ER - TY - THES A1 - Neumann, Bettina T1 - Bioelectrocatalytic activity of surface-confined heme catalysts BT - from natural enzymes to synthetic analogs Y1 - 2019 ER - TY - THES A1 - Schröder, Ariane T1 - Biological Inf(1)ections of the American Dream BT - Contagious Disease and Narrative Containment in U.S. American Literature and Culture Y1 - 2019 SN - 978-3-643-91274-9 PB - Lit CY - Wien ER - TY - JOUR A1 - Bornhorst, Dorothee A1 - Xia, Peng A1 - Nakajima, Hiroyuki A1 - Dingare, Chaitanya A1 - Herzog, Wiebke A1 - Lecaudey, Virginie A1 - Mochizuki, Naoki A1 - Heisenberg, Carl-Philipp A1 - Yelon, Deborah A1 - Abdelilah-Seyfried, Salim T1 - Biomechanical signaling within the developing zebrafish heart attunes endocardial growth to myocardial chamber dimensions JF - Nature Communications N2 - Intra-organ communication guides morphogenetic processes that are essential for an organ to carry out complex physiological functions. In the heart, the growth of the myocardium is tightly coupled to that of the endocardium, a specialized endothelial tissue that lines its interior. Several molecular pathways have been implicated in the communication between these tissues including secreted factors, components of the extracellular matrix, or proteins involved in cell-cell communication. Yet, it is unknown how the growth of the endocardium is coordinated with that of the myocardium. Here, we show that an increased expansion of the myocardial atrial chamber volume generates higher junctional forces within endocardial cells. This leads to biomechanical signaling involving VE-cadherin, triggering nuclear localization of the Hippo pathway transcriptional regulator Yap1 and endocardial proliferation. Our work suggests that the growth of the endocardium results from myocardial chamber volume expansion and ends when the tension on the tissue is relaxed. Y1 - 2019 U6 - https://doi.org/10.1038/s41467-019-12068-x SN - 2041-1723 VL - 10 PB - Nature Publ. Group CY - London ER -