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Search: WFRF:(Kern Zoltan) > (2020-2022)

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1.
  • Haszpra, Laszlo, et al. (author)
  • Real-world wintertime CO, N2O, and CO2 emissions of a central European village
  • 2022
  • In: Atmospheric Measurement Techniques. - : Copernicus GmbH. - 1867-8548. ; 15:17, s. 5019-5031
  • Journal article (peer-reviewed)abstract
    • Although small rural settlements are only minor individual sources of greenhouse gases and air pollution, their high overall occurrence can significantly contribute to the total emissions of a region or country. Emissions from a rural lifestyle may be remarkably different than those of urban and industrialized regions, but nevertheless they have hardly been studied so far. Here, flux measurements at a tall-tower eddy covariance monitoring site and the footprint model FFP are used to determine the real-world wintertime CO, N2O, and CO2 emissions of a small village in western Hungary. The recorded emission densities, dominantly resulting from residential heating, are 3.5, 0.043, and 72 μg m-2 s-1 for CO, N2O, and CO2, respectively. While the measured CO and CO2 emissions are comparable to those calculated using the assumed energy consumption and applying the according emission factors, the nitrous oxide emissions exceed the expected value by a magnitude. This may indicate that the nitrous oxide emissions are significantly underestimated in the emission inventories, and modifications in the methodology of emission calculations are necessary. Using a three-dimensional forward transport model, we further show that, in contrast to the flux measurements, the concentration measurements at the regional background monitoring site are only insignificantly influenced by the emissions of the nearby village.
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2.
  • Megyesfalvi, Zsolt, et al. (author)
  • Expression patterns and prognostic relevance of subtype-specific transcription factors in surgically resected small-cell lung cancer : an international multicenter study
  • 2022
  • In: Journal of Pathology. - : Wiley. - 0022-3417 .- 1096-9896. ; 257:5, s. 674-686
  • Journal article (peer-reviewed)abstract
    • The tissue distribution and prognostic relevance of subtype-specific proteins (ASCL1, NEUROD1, POU2F3, YAP1) present an evolving area of research in small-cell lung cancer (SCLC). The expression of subtype-specific transcription factors and P53 and RB1 proteins were measured by immunohistochemistry (IHC) in 386 surgically resected SCLC samples. Correlations between subtype-specific proteins and in vitro efficacy of various therapeutic agents were investigated by proteomics and cell viability assays in 26 human SCLC cell lines. Besides SCLC-A (ASCL1-dominant), SCLC-AN (combined ASCL1/NEUROD1), SCLC-N (NEUROD1-dominant), and SCLC-P (POU2F3-dominant), IHC and cluster analyses identified a quadruple-negative SCLC subtype (SCLC-QN). No unique YAP1-subtype was found. The highest overall survival rates were associated with non-neuroendocrine subtypes (SCLC-P and SCLC-QN) and the lowest with neuroendocrine subtypes (SCLC-A, SCLC-N, SCLC-AN). In univariate analyses, high ASCL1 expression was associated with poor prognosis and high POU2F3 expression with good prognosis. Notably, high ASCL1 expression influenced survival outcomes independently of other variables in a multivariate model. High POU2F3 and YAP1 protein abundances correlated with sensitivity and resistance to standard-of-care chemotherapeutics, respectively. Specific correlation patterns were also found between the efficacy of targeted agents and subtype-specific protein abundances. In conclusion, we investigated the clinicopathological relevance of SCLC molecular subtypes in a large cohort of surgically resected specimens. Differential IHC expression of ASCL1, NEUROD1, and POU2F3 defines SCLC subtypes. No YAP1-subtype can be distinguished by IHC. High POU2F3 expression is associated with improved survival in a univariate analysis, whereas elevated ASCL1 expression is an independent negative prognosticator. Proteomic and cell viability assays of human SCLC cell lines revealed distinct vulnerability profiles defined by transcription regulators.
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