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  • 1
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    Unknown
    Leiden, etc. : Periodicals Archive Online (PAO)
    Mnemosyne. ser.4:48:5 (1995:Nov.) 565 
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Archives of environmental contamination and toxicology 36 (1999), S. 242-247 
    ISSN: 1432-0703
    Source: Springer Online Journal Archives 1860-2000
    Topics: Energy, Environment Protection, Nuclear Power Engineering , Medicine
    Notes: Abstract. The sorption of volatile organic analytes from water samples by the Teflon septum surface used with standard glass 40-ml sample collection vials was investigated. Analytes tested included alkanes, isoalkanes, olefins, cycloalkanes, a cycloalkene, monoaromatics, a polynuclear aromatic, and two chloroethenes. Both laboratory prepared test mix solutions and petroleum contaminated groundwater from three field sites were tested. A rapid loss of n-alkane and isoalkane concentrations (〉10%) was observed within 24 h when stored at room temperature. Aliphatic losses were also observed (〉10%) over a 21-day holding period when samples were held at 4°C. Loss of the less sorptive analytes was demonstrated by exposing analyte solutions to greater Teflon surface areas. The demonstrated sorption of aliphatics from water samples by Teflon-lined septa indicates that the accuracy of volatile petroleum hydrocarbon determinations may be reduced by the traditional storage method. An alternative storage protocol is reported combining a lead foil septum surface and 1% (w/w) tribasic sodium phosphate dodecahydrate (Na3PO4 · 12H2O) preservative. This method prevented loss of the test analytes, including alkanes and isoalkanes for at least 21 days at room temperature.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Cellular and molecular life sciences 54 (1998), S. 902-909 
    ISSN: 1420-9071
    Keywords: Key words. PS1; presenilin-1; Alzheimer's disease; FAD; neurodegeneration; β-amyloid; mutations.
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract. Presenilin-1 (PS1) mutations account for the greatest portion of early onset familial Alzheimer's disease (FAD) cases. The exact cellular function of PS1 is not known. To date, PS1 mutations have been shown to alter two potential biological roles of the protein, either of which could make neurons more susceptible to neurodegeneration. First, PS1 mutations result in elevated Aβ42/Aβ40 ratios in plasma of FAD patients, in transgenic mice and in transfected cell lines. Aβ42 is the more hydrophobic and most neurotoxic form of the peptide. A common molecular event that has been associated with all of the known early onset FAD genes is the excessive production or accumulation of the Aβ peptide in the brain. PS1 mutations have also been found to alter the Notch signalling pathway, but the mechanism by which this may affect neurodegeneration remains to be determined. Future studies will be needed to elucidate whether PS1 mutations lead directly to neuronal dysfunction and degeneration or cause cell death by increasing Aβ42 generation and deposition.
    Type of Medium: Electronic Resource
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