Eschatology in Contemporary German Lyrical Poetry

For this paper I have selected three contemporary authors whose texts are representative of the latest trends in German lyric poetry- or more precisely, lyric poetry in the German language: Durs Grünbein, Richard Exner and Erich Fried. Ours Grilnbein stands for a recent poetic trend that blends in (East German) Marxism, nihilism and postmodern ideas. Richard Exner, an American Germanist, explores some poetical discourses of Judea-Christian mythology whilst Erich Fried writes in the tradition of (Western) Socialism, Judaism and 19th century German Idealism

Pluralität und Pluralismus: Zu Kontexten und Grundformen des christlich-islamischen Dialogs in Deutschland

The fact that Islam is now the second religion of Germany, as with much of Western Europe, raises profound questions. What does it mean for the self-understanding of both Christians and Germans within Germany, as well as for the life of the nation? What constitute key impacts and effects of this relatively new situation? What are the consequences for understanding and thinking? And what comprises the key context for the situation of, as well as critical reflection upon, the phenomenon and development of Christian–Muslim interreligious dialogue? In this paper the authors explore dimensions of the fact of plurality and the cognitive response to it that issues in the paradigm of pluralism. The paper takes account of critical theological and philosophical considerations together with the perspectives of cultural theory and reflection upon the context of Christian-Muslim dialogical engagement in Germany

Dimensional Complexity of the Resting Brain in Healthy Aging, Using a Normalized MPSE

Spontaneous fluctuations of resting-state functional connectivity have been studied in many ways, but grasping the complexity of brain activity has been difficult. Dimensional complexity measures, which are based on Eigenvalue (EV) spectrum analyses (e.g., Ω entropy) have been successfully applied to EEG data, but have not been fully evaluated on functional MRI recordings, because only through the recent introduction of fast multiband fMRI sequences, feasable temporal resolutions are reached. Combining the Eigenspectrum normalization of Ω entropy and the scalable architecture of the so called Multivariate Principal Subspace Entropy (MPSE) leads to a new complexity measure, namely normalized MPSE (nMPSE). It allows functional brain complexity analyses at varying levels of EV energy, independent from global shifts in data variance. Especially the restriction of the EV spectrum to the first dimensions, carrying the most prominent data variance, can act as a filter to reveal the most discriminant factors of dependent variables. Here we look at the effects of healthy aging on the dimensional complexity of brain activity. We employ a large open access dataset, providing a great number of high quality fast multiband recordings. Using nMPSE on whole brain, regional, network and searchlight approaches, we were able to find many age related changes, i.e., in sensorimotoric and right inferior frontal brain regions. Our results implicate that research on dimensional complexity of functional MRI recordings promises to be a unique resource for understanding brain function and for the extraction of biomarkers

Exploration of the TRIM fold of MuRF1 using EPR reveals a canonical antiparallel structure and extended COS-box

MuRF1 (TRIM63) is a RING-type E3 ubiquitin ligase with a predicted tripartite TRIM fold. TRIM proteins rely upon the correct placement of an N-terminal RING domain, with respect to C-terminal, specific substrate-binding domains. The TRIM domain organization is orchestrated by a central helical domain that forms an antiparallel coiled-coil motif and mediates the dimerization of the fold. MuRF1 has a reduced TRIM composition characterized by a lack of specific substrate binding domains, but contains in its helical domain a conserved sequence motif termed COS-box that has been speculated to fold independently into an α-hairpin. These characteristics had led to question whether MuRF1 adopts a canonical TRIM fold. Using a combination of electron paramagnetic resonance, on spin-labeled protein, and disulfide crosslinking, we show that TRIM63 follows the structural conservation of the TRIM dimerization domain, observed in other proteins. We also show that the COS-box motif folds back onto the dimerization coiled-coil motif, predictably forming a four-helical bundle at the center of the protein and emulating the architecture of canonical TRIMs.publishe

Portfolio Vol. III N 1

Metcalf, Caroline. Master of the World. Prose. 3-5. Phillips, Alison. Eulogies. Poetry. 6. Chadeayne, Robert O. Oak Street. Picture. 6. Bethune, Don. Denisonism. Prose. 7-8. Maxwell, Bob. My Star. Prose. 9-11. V_______, S_______. Poet Philosopher. Poetry. 12. Ewart, Alison. Pious Fraud. Prose. 13-15. Beckham, Adela. Reflections. Poetry. 16. Velicka, Edward. Portrait. Picture. 16. Deane, Dorothy. Review of New Books. Prose. 17. Smith, Bob. Review of New Recordings. Prose. 17. Franke, Ruth. Original Designs. Picture. 18. Black, Jim. Drama. Prose. 19-20. Nadel, Norman S. Initial Plunge. Prose. 23-24

Genetic Variation in ABCC4 and CFTR and Acute Pancreatitis during Treatment of Pediatric Acute Lymphoblastic Leukemia

Background: Acute pancreatitis (AP) is a serious, mechanistically not entirely resolved side effect of L-asparaginase-containing treatment for acute lymphoblastic leukemia (ALL). To find new candidate variations for AP, we conducted a genome-wide association study (GWAS). Methods: In all, 1,004,623 single-nucleotide variants (SNVs) were analyzed in 51 pediatric ALL patients with AP (cases) and 1388 patients without AP (controls). Replication used independent patients. Results: The top-ranked SNV (rs4148513) was located within the ABCC4 gene (odds ratio (OR) 84.1; p = 1.04 × 10−14). Independent replication of our 20 top SNVs was not supportive of initial results, partly because rare variants were neither present in cases nor present in controls. However, results of combined analysis (GWAS and replication cohorts) remained significant (e.g., rs4148513; OR = 47.2; p = 7.31 × 10−9). Subsequently, we sequenced the entire ABCC4 gene and its close relative, the cystic fibrosis associated CFTR gene, a strong AP candidate gene, in 48 cases and 47 controls. Six AP-associated variants in ABCC4 and one variant in CFTR were detected. Replication confirmed the six ABCC4 variants but not the CFTR variant. Conclusions: Genetic variation within the ABCC4 gene was associated with AP during the treatment of ALL. No association of AP with CFTR was observed. Larger international studies are necessary to more conclusively assess the risk of rare clinical phenotypes

The ICON-A model for direct QBO simulations on GPUs (version icon-cscs:baf28a514)

Classical numerical models for the global atmosphere, as used for numerical weather forecasting or climate research, have been developed for conventional central processing unit (CPU) architectures. This hinders the employment of such models on current top-performing supercomputers, which achieve their computing power with hybrid architectures, mostly using graphics processing units (GPUs). Thus also scientific applications of such models are restricted to the lesser computer power of CPUs. Here we present the development of a GPU-enabled version of the ICON atmosphere model (ICON-A), motivated by a research project on the quasi-biennial oscillation (QBO), a global-scale wind oscillation in the equatorial stratosphere that depends on a broad spectrum of atmospheric waves, which originates from tropical deep convection. Resolving the relevant scales, from a few kilometers to the size of the globe, is a formidable computational problem, which can only be realized now on top-performing supercomputers. This motivated porting ICON-A, in the specific configuration needed for the research project, in a first step to the GPU architecture of the Piz Daint computer at the Swiss National Supercomputing Centre and in a second step to the JUWELS Booster computer at the Forschungszentrum Jülich. On Piz Daint, the ported code achieves a single-node GPU vs. CPU speedup factor of 6.4 and allows for global experiments at a horizontal resolution of 5 km on 1024 computing nodes with 1 GPU per node with a turnover of 48 simulated days per day. On JUWELS Booster, the more modern hardware in combination with an upgraded code base allows for simulations at the same resolution on 128 computing nodes with 4 GPUs per node and a turnover of 133 simulated days per day. Additionally, the code still remains functional on CPUs, as is demonstrated by additional experiments on the Levante compute system at the German Climate Computing Center. While the application shows good weak scaling over the tested 16-fold increase in grid size and node count, making also higher resolved global simulations possible, the strong scaling on GPUs is relatively poor, which limits the options to increase turnover with more nodes. Initial experiments demonstrate that the ICON-A model can simulate downward-propagating QBO jets, which are driven by wave–mean flow interaction

Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia.

Carriers of large recurrent copy number variants (CNVs) have a higher risk of developing neurodevelopmental disorders. The 16p11.2 distal CNV predisposes carriers to e.g., autism spectrum disorder and schizophrenia. We compared subcortical brain volumes of 12 16p11.2 distal deletion and 12 duplication carriers to 6882 non-carriers from the large-scale brain Magnetic Resonance Imaging collaboration, ENIGMA-CNV. After stringent CNV calling procedures, and standardized FreeSurfer image analysis, we found negative dose-response associations with copy number on intracranial volume and on regional caudate, pallidum and putamen volumes (β = -0.71 to -1.37; P < 0.0005). In an independent sample, consistent results were obtained, with significant effects in the pallidum (β = -0.95, P = 0.0042). The two data sets combined showed significant negative dose-response for the accumbens, caudate, pallidum, putamen and ICV (P = 0.0032, 8.9 × 10-6, 1.7 × 10-9, 3.5 × 10-12 and 1.0 × 10-4, respectively). Full scale IQ was lower in both deletion and duplication carriers compared to non-carriers. This is the first brain MRI study of the impact of the 16p11.2 distal CNV, and we demonstrate a specific effect on subcortical brain structures, suggesting a neuropathological pattern underlying the neurodevelopmental syndromes