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Träfflista för sökning "WFRF:(Simon Philipp) srt2:(2010-2014)"

Sökning: WFRF:(Simon Philipp) > (2010-2014)

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1.
  • Fäh, Donat, et al. (författare)
  • Coupled seismogenic geohazards in Alpine regions
  • 2012
  • Ingår i: Bollettino di Geofisica Teorica ed Applicata. - 0006-6729. ; 53:4, s. 485-508
  • Tidskriftsartikel (refereegranskat)abstract
    • COupled seismogenic GEohazards in Alpine Regions (COGEAR) is an interdisciplinary natural hazard project investigating the hazard chain induced by earthquakes. It addresses tectonic processes and the related variability of seismicity in space and time, earthquake forecasting and short-term precursors, and strong ground motion as a result of source and complex path effects. We study non-linear wave propagation phenomena, liquefaction and triggering of landslides in soil and rock, as well as earthquake-induced snow avalanches. The Valais, and in particular parts of the Rhone, Visper, and Matter valleys have been selected as study areas. Tasks include detailed field investigations, development and application of numerical modeling techniques, assessment of the susceptibility to seismically induced effects, and installation of different monitoring systems to test and validate our models. These systems are for long-term operation and include a continuous GPS and seismic networks, a test installation for observing earthquake precursors, and a system to study site-effects and non-linear phenomena in two test areas (Visp, St. Niklaus / Randa). Risk-related aspects relevant for buildings and lifelines are also considered
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3.
  • Neudecker, Philipp, et al. (författare)
  • Structure of an Intermediate State in Protein Folding and Aggregation
  • 2012
  • Ingår i: Science. - : American Association for the Advancement of Science. - 0036-8075 .- 1095-9203. ; 336:5079, s. 362-366
  • Tidskriftsartikel (refereegranskat)abstract
    • Protein-folding intermediates have been implicated in amyloid fibril formation involved in neurodegenerative disorders. However, the structural mechanisms by which intermediates initiate fibrillar aggregation have remained largely elusive. To gain insight, we used relaxation dispersion nuclear magnetic resonance spectroscopy to determine the structure of a low-populated, on-pathway folding intermediate of the A39V/N53P/V55L (A, Ala; V, Val; N, Asn; P, Pro; L, Leu) Fyn SH3 domain. The carboxyl terminus remains disordered in this intermediate, thereby exposing the aggregation-prone amino-terminal beta strand. Accordingly, mutants lacking the carboxyl terminus and thus mimicking the intermediate fail to safeguard the folding route and spontaneously form fibrillar aggregates. The structure provides a detailed characterization of the non-native interactions stabilizing an aggregation-prone intermediate under native conditions and insight into how such an intermediate can derail folding and initiate fibrillation.
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4.
  • Thompson, Paul M., et al. (författare)
  • The ENIGMA Consortium : large-scale collaborative analyses of neuroimaging and genetic data
  • 2014
  • Ingår i: BRAIN IMAGING BEHAV. - : Springer Science and Business Media LLC. - 1931-7557 .- 1931-7565. ; 8:2, s. 153-182
  • Tidskriftsartikel (refereegranskat)abstract
    • The Enhancing NeuroImaging Genetics through Meta-Analysis (ENIGMA) Consortium is a collaborative network of researchers working together on a range of large-scale studies that integrate data from 70 institutions worldwide. Organized into Working Groups that tackle questions in neuroscience, genetics, and medicine, ENIGMA studies have analyzed neuroimaging data from over 12,826 subjects. In addition, data from 12,171 individuals were provided by the CHARGE consortium for replication of findings, in a total of 24,997 subjects. By meta-analyzing results from many sites, ENIGMA has detected factors that affect the brain that no individual site could detect on its own, and that require larger numbers of subjects than any individual neuroimaging study has currently collected. ENIGMA's first project was a genome-wide association study identifying common variants in the genome associated with hippocampal volume or intracranial volume. Continuing work is exploring genetic associations with subcortical volumes (ENIGMA2) and white matter microstructure (ENIGMA-DTI). Working groups also focus on understanding how schizophrenia, bipolar illness, major depression and attention deficit/hyperactivity disorder (ADHD) affect the brain. We review the current progress of the ENIGMA Consortium, along with challenges and unexpected discoveries made on the way.
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