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  • 1
    Electronic Resource
    Electronic Resource
    Gravimetric Determination of Zirconium in Titanium (1959)
    s.l. : American Chemical Society
    Analytical chemistry 31 (1959), S. 252-254 
    Details
    ISSN: 1520-6882
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1021/ac60146a029
    Library Location Call Number Volume/Issue/Year Availability
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    Paper (German National Licenses)
    Fulltext
  • 2
    Electronic Resource
    Electronic Resource
    Language and World View (1992)
    Palo Alto, Calif. : Annual Reviews
    Annual Review of Anthropology 21 (1992), S. 381-404 
    Details
    ISSN: 0084-6570
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Ethnic Sciences , Biology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1146/annurev.an.21.100192.002121
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    Paper (German National Licenses)
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  • 3
    Electronic Resource
    Electronic Resource
    Genetic engineering of plants for virus resistance (1990)
    Springer
    Archives of virology 115 (1990), S. 1-21 
    Details
    ISSN: 1432-8798
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Historically, control of plant virus disease has involved numerous strategies which have often been combined to provide effective durable resistance in the field. In recent years, the dramatic advances obtained in plant molecular virology have enhanced our understanding of viral genome organizations and gene functions. Moreover, genetic engineering of plants for virus resistance has recently provided promising additional strategies for control of virus disease. At present, the most promising of these has been the expression of coat-protein coding sequences in plants transformed with a coat protein gene. Other potential methods include the expression of anti-sense viral transcripts in transgenic plants, the application of artificial anti-sense mediated gene regulation to viral systems, and the expression of viral satellite RNAs, RNAs with endoribonuclease activity, antiviral antibody genes, or human interferon genes in plants.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF01310619
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    Paper (German National Licenses)
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  • 4
    Electronic Resource
    Electronic Resource
    Molecular basis for virus disease resistance in plants (1993)
    Springer
    Archives of virology 131 (1993), S. 1-16 
    Details
    ISSN: 1432-8798
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Classical studies of virus disease resistance in plants have provided the basis for recent molecular studies of resistance. Three common approaches to the study of resistance have been used. In one approach, nucleotide and/or amino acid sequences of virus strains that overcome disease resistance genes in the host are compared with sequences of strains that do not induce disease in these hosts. In the second approach, resistance/susceptibility of protoplasts is compared with the response of intact plants from which they are derived, to develop hypotheses regarding whether resistance acts at the level of the individual cell or by inhibiting cell-to-cell movement. In the third approach, the mechanism of virus cell-to-cell movement has been studied to clarify one of the basic steps in pathogenesis and to determine the mechanism of disease resistance for certain virus-host interactions.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF01379076
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    Paper (German National Licenses)
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  • 5
    Electronic Resource
    Electronic Resource
    A simple, efficient, standard-dilution method for cloning hybridomas (1987)
    Springer
    Biotechnology techniques 1 (1987), S. 31-33 
    Details
    ISSN: 1573-6784
    Source: Springer Online Journal Archives 1860-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary A simple standard-dilution method which obviates routine use of viable cell counts, feeder layers and time-consuming scale-up procedures is described. This method can be used to clone monoclonal antibody-producing hybridomas 9–14 days post-fusion. Each cloning cycle takes 5 min. Approximately 60% of the positive, monoclonal antibody-producing hybridomas were successfully cloned and established.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00156283
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    Paper (German National Licenses)
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