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  • recombinant inbred  (2)
  • Area postrema  (1)
  • CO oxidation  (1)
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  • 1
    ISSN: 1572-879X
    Keywords: Au/Fe2O3 catalyst ; structural study ; CO oxidation ; mechanism of the structural changes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract 1 wt% Au/Fe2O3 catalyst was prepared by a co‐precipitation method. The structure of the sample in the as prepared, oxidized and reduced states was investigated by means of X‐ray photoelectron spectroscopy (XPS), transition electron microscopy (TEM), electron diffraction (ED) and X‐ray diffraction (XRD). The structure of the samples after various treatments and their activity in the CO oxidation were compared. The results show the stability of the gold particle size during the treatments. However, after oxidation, a slight shift in the Au 4f binding energy towards lower values points to the formation of an electron‐rich state of the metallic gold particles compared to that revealed in the as prepared sample. Simultaneously, a goethite phase in the Fe2O3 support is present, which is not observed in the “as prepared” and reduced samples. In the reduced sample the presence of a crystalline maghemite‐c phase indicates a change in the support morphology. In the CO oxidation the oxidized sample shows the highest activity and it might be the result of the cooperative effect of goethite, FeO and the electron‐rich metallic gold nanoparticles. We suggest that a structural transformation occurs along the gold/support perimeter during the treatments and we propose a possible mechanism for the effect of the oxidation treatment.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Acta neuropathologica 75 (1987), S. 16-22 
    ISSN: 1432-0533
    Keywords: Monosodium-l-glutamate ; Neuronal death ; Area postrema ; Acetylcholinesterase ; Fetal rats
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Monosodium-l-glutamate given subcutaneously to pregnant rats caused acute necrosis of the acetylcholinesterase-positive neurons in the area postrema. The same effect has been observed in the area postrema of fetal rats. The process of neuronal cell death and the elimination of debris by microglia cells proved to be similar in pregnant animals and in their fetuses. However, embryonal neurons were more sensitive to glutamate as judged by the rapidity of the process and the dose-response relationship. These observations raise the possibility of transplacental poisoning in human fetuses after the consumption of glutamate-rich food by the mother.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Behavior genetics 29 (1999), S. 339-348 
    ISSN: 1573-3297
    Keywords: Sleep ; influenza ; virus ; recombinant inbred ; C57BL/6 ; BALB/cBy ; QTL
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Psychology
    Notes: Abstract Influenza-infected C57BL/6J mice spend increased amounts of time in slow-wave sleep (SWS) during the dark phase of the circadian cycle compared to healthy mice. In contrast, infected BALB/cByJ mice show a normal or reduced time in SWS, particularly during the light phase. To identify genetic loci with linkage to these traits, we measured sleep in 13 CXB recombinant inbred (RI) strains derived from a cross between C57BL/6ByJ and BALB/cByJ mice. The probability density distribution of sleep patterns of influenza-infected CXB RI mice showed modes that correspond roughly with the parental modes during the dark phase of the circadian cycle and are intermediate or C57BL/6-like during the light phase. These patterns are consistent with the presence of a low number of major effect quantitative trait loci (QTLs). Chromosomal regions with provisional association to strain variation in influenza-induced SWS patterns were identified. In particular, a 10- to 12-cM interval on Chr 6 between D6Mit74 and D6Mit188 contains a QTL (LRS = 16.6 at 1 cM proximal to D6Mit316; genomewide p〈.05) that influences the SWS response to influenza infection during the light phase. We have provisionally named this QTL Srilp1 (sleep response to influenza, light phase 1). Candidate genes for mediation of this phenotype include Ghrhr (growth hormone releasing hormone receptor), Crhr2 (corticotropin releasing hormone receptor 2), and Cd8a (an epitope on cytotoxic T lymphocytes). Several other intervals achieved suggestive probability scores that are sufficient to warrant further analysis either with additional RI strains or with F2 panels. The analysis also suggests that dark phase and light phase responses are regulated by different genetic factors.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Behavior genetics 29 (1999), S. 329-337 
    ISSN: 1573-3297
    Keywords: Sleep ; REM sleep ; mice ; recombinant inbred ; QTL ; BALB/cBy ; C57BL/6
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Psychology
    Notes: Abstract Various inbred strains of mice show different daily amounts of slow-wave sleep (SWS) and rapid-eye movement sleep (REMS), suggesting the possibility of genetic influences on sleep propensity. Previous work by others studying the spontaneous sleep patterns of seven strains of CXB recombinant inbred (RI) mice suggested several candidate quantitative trait loci (QTLs) associated with variation in REMS. Extending this approach, we evaluated the sleep patterns of 13 CXB RI strains and conducted linkage analyses based on 223 discrete informative loci. The probability density distribution of light phase REMS for the CXB RI strains showed deflections that correspond approximately to the parental phenotypes. This type of pattern is consistent with the presence of a low number of major effect quantitative trait loci. Regions of chromosomes 4, 16, and 17 showed provisional linkage to strain variation in REMS. The distribution of loci further suggested that dark phase and light phase REMS may be regulated by different genetic factors. Probabilities of linkage were not sufficient for declaration of a quantitative trait locus for REMS but were sufficient to warrant further analysis either with additional RI strains or with F2 panels.
    Type of Medium: Electronic Resource
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