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Träfflista för sökning "(WFRF:(Carlsson E.)) pers:(Johansson E) srt2:(2000-2004)"

Sökning: (WFRF:(Carlsson E.)) pers:(Johansson E) > (2000-2004)

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  • Ahnberg, H., et al. (författare)
  • Stabilising effects of different binders in some Swedish soils
  • 2003
  • Ingår i: Ground Improvement. - : Thomas Telford Ltd.. - 1365-781X .- 1751-7621. ; 7:1, s. 9-23
  • Tidskriftsartikel (refereegranskat)abstract
    • In Sweden, lime and lime-cement have been used for several decades as stabilising agents in deep stabilisation of soft soils. More recently, other types of binder have come into use, but so far only to a limited extent. In order to gather experience about the effect of various binders, laboratory tests have been performed on different types of soil stabilised with a range of binders. Lime, cement, fly ash and blast furnace slag in different combinations together with different admixtures, such as gypsum, silica fume and calcium chloride, have been used in the investigations. The variation in strength with type of binder has been studied, and comparisons have also been made with results from some previous investigations using different binders. The tests showed that there is no optimal, universal binder for stabilisation of the soils. Whereas some binders are robust, yielding good results in most types of soil, there are also binders that produce very good results in certain soils but poor results in others. Both similarities and differences in effects were found for different binders.
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  • Tentler, Dmitry, et al. (författare)
  • A candidate region for Asperger syndrome defined by two 17p breakpoints
  • 2003
  • Ingår i: European Journal of Human Genetics. - : Springer Science and Business Media LLC. - 1018-4813 .- 1476-5438. ; 11:2, s. 189-195
  • Tidskriftsartikel (refereegranskat)abstract
    • Asperger syndrome (AS) is a mild form of autistic disorder characterised by impairment in social interaction as well as a restricted pattern of behaviour, interests, and activities. Two patients with AS and balanced translocations t(13;17) and t(17;19), respectively, were identified. Fluorescent in situ hybridisation (FISH) analysis with chromosome 17 specific clones to metaphase chromosomes from both patients showed that the chromosome 17 breakpoints are located within a 300 kb region at 17p13. The region spans 14 known genes. The expression of these genes was analysed in lymphoblastoid RNA derived from the patients and healthy control individuals. The CHRNE, DKFZP566H073, LOC90048, PFN1, SPAG7, KIAA0909, ZNF232 and KIF1C genes showed similar levels of expression in cell lines with the translocations when compared with cell lines with normal karyotype. No expression was detected for the MINK, GP1BA, SLC25A11, ENO3, FLJ10060 and USP6 genes in any of the cell lines. The close physical relation of the two 17p breakpoints suggest a common genetic aetiology for the phenotype in the patients. Structural and functional analysis of the genes located around the two 17p breakpoints in t(13;17) and t(17;19) patients may reveal candidate sequences for the AS phenotype.
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