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Träfflista för sökning "WFRF:(Clausen Jonas) srt2:(2010-2014)"

Sökning: WFRF:(Clausen Jonas) > (2010-2014)

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1.
  • Clausen Mork, Jonas (författare)
  • Dealing with uncertainty
  • 2012
  • Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
    • Uncertainty is, it seems, more or less constantly present in our lives. Even so, grasping the concept philosophically is far from trivial. In this doctoral thesis, uncertainty and its conceptual companion information are studied. Axiomatic analyses are provided and numerical measures suggested. In addition to these basic conceptual analyses, the widespread practice of so-called safety factor use in societal regulation is analyzed along with the interplay between science and policy in European regulation of chemicals and construction.
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2.
  • Clausen Mork, Jonas (författare)
  • Uncertainty, credal sets and second order probability
  • 2013
  • Ingår i: Synthese. - : Springer Science and Business Media LLC. - 0039-7857 .- 1573-0964. ; 190:3, s. 353-378
  • Tidskriftsartikel (refereegranskat)abstract
    • The last 20 years or so has seen an intense search carried out within Dempster–Shafer theory, with the aim of finding a generalization of the Shannon entropy for belief functions. In that time, there has also been much progress made in credal set theory—another generalization of the traditional Bayesian epistemic representation—albeit not in this particular area. In credal set theory, sets of probability functions are utilized to represent the epistemic state of rational agents instead of the single probability function of traditional Bayesian theory. The Shannon entropy has been shown to uniquely capture certain highly intuitive properties of uncertainty, and can thus be considered a measure of that quantity. This article presents two measures developed with the purpose of generalizing the Shannon entropy for (1) unordered convex credal sets and (2) possibly non-convex credal sets ordered by second order probability, thereby providing uncertainty measures for such epistemic representations. There is also a comparison with the results of the measure AU developed within Dempster–Shafer theory in a few instances where unordered convex credal set theory and Dempster–Shafer theory overlap.
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3.
  • Hillered, Lars, et al. (författare)
  • Cerebral microdialysis for protein biomarker monitoring in the neurointensive care setting - a technical approach
  • 2014
  • Ingår i: Frontiers in Neurology. - : Frontiers Media SA. - 1664-2295. ; 5, s. 245-
  • Tidskriftsartikel (refereegranskat)abstract
    • Cerebral microdialysis (MD) was introduced as a neurochemical monitoring method in the early 1990s and is currently widely used for the sampling of low molecular weight molecules, signaling energy crisis, and cellular distress in the neurointensive care (NIC) setting. There is a growing interest in MD for harvesting of intracerebral protein biomarkers of secondary injury mechanisms in acute traumatic and neurovascular brain injury in the NIC community. The initial enthusiasm over the opportunity to sample protein biomarkers with high molecular weight cut-off MD catheters has dampened somewhat with the emerging realization of inherent methodological problems including protein-protein interaction, protein adhesion, and biofouling, causing an unstable in vivo performance (i.e., fluid recovery and extraction efficiency) of the MD catheter. This review will focus on the results of a multidisciplinary collaborative effort, within the Uppsala Berzelii Centre for Neurodiagnostics during the past several years, to study the features of the complex process of high molecular weight cut-off MD for protein biomarkers. This research has led to new methodology showing robust in vivo performance with optimized fluid recovery and improved extraction efficiency, allowing for more accurate biomarker monitoring. In combination with evolving analytical methodology allowing for multiplex biomarker analysis in ultra-small MD samples, a new opportunity opens up for high-resolution temporal mapping of secondary injury cascades, such as neuroinflammation and other cell injury reactions directly in the injured human brain. Such data may provide an important basis for improved characterization of complex injuries, e.g., traumatic and neurovascular brain injury, and help in defining targets and treatment windows for neuroprotective drug development.
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