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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Archives of microbiology 97 (1974), S. 27-38 
    ISSN: 1432-072X
    Keywords: Mass Mating ; Electron Microscopy ; Cell Fusion ; Membrane Structure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The process of mating reaction of Saccharomyces cerevisiae was studied by electron microscopy. Prior to the dissolution of the part of the cell walls separating the conjugating pair of cells, the thinning of the electron transparent layer of the cell wall occurs at the part toward which the nuclei are migrating. After the dissolution of the cell walls of the conjugating cells, the cell membranes become associated with each other, then to be broken and rejoined. The first diploid bud emerges from about the middle of the zygote. The morphological changes during the mating reaction are discussed in relation to the biochemical changes so far known.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of infection and chemotherapy 6 (2000), S. 35-40 
    ISSN: 1437-7780
    Keywords: Key words L929 fibroblast ; Itraconazole (ITCZ) ; Cell membrane ; Antifungal agents ; Vincristine ; Scanning electron microscopy (SEM)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Itraconazole (ITCZ), a triazole antifungal agent, was studied for its effects on the morphology and function of L929 fibroblasts. L929 fibroblasts were cultured for 20 h with ITCZ or one of several other triazoles (fluconazole, ketoconazole, and hydroxy-itraconazole [ITCZ-OH]) at the concentration of 0.5 μg/ml. Among these agents, only ITCZ and its metabolite ITCZ-OH markedly elongated the cells bidirectionally. Scanning electron microscopy studies showed that the surface of the elongated cells was smoother than that of the untreated cells. The viability of L929 cells cultured with 0.5 μg/ml of ITCZ for 20 h was not lowered. However, after treatment with 0.0375% sodium deoxycholate (DOC) solution, the viability of the cells treated with ITCZ, as evaluated by the 3-(4,5-dimethyl-2thiazoyl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) proliferation assay or the release of lactic dehydrogenase from cytoplasm, was decreased. When L929 cells were cultured in the presence of a combination of ITCZ and vincristine, their growth was synergistically inhibited. This synergism was also observed when ITCZ was replaced by ITCZ-OH, but not by the other azoles. These findings suggest that the exposure of L929 fibroblasts to low ITCZ concentrations affects the physiological nature of their cell membrane.
    Type of Medium: Electronic Resource
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