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  • Articles: DFG German National Licenses  (2)
  • 1970-1974  (2)
  • 1971  (1)
  • 1970  (1)
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  • Articles: DFG German National Licenses  (2)
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Years
  • 1970-1974  (2)
Year
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of cancer research and clinical oncology 76 (1971), S. 1-7 
    ISSN: 1432-1335
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung Die im obigen Titel erwähnten, drei nutritiv bedeutenden Endiol-Verbindungen können Sarkom-180 hemmen. Die hemmende Wirksamkeit von Ascorbinsäure wird durch Cupri-Ionen verstärkt. Diese Endiolen depolymerisieren DNS, besonders unter Mitwirkung von Kupfer. Dehydroascorbinsäure besitzt die Fähigkeit, denaturierte DNS zu brechen und eine einstrangige Spaltung für native Nucleinsäure zu bewirken. Eine Mischung von Dehydroascorbat und Cu zersetzt Apurinsäure und trennt daraus Deoxy-cyctidylsäure. Nur die Oligo-Form von Pyrimidin-Tetra- und Penta-Nucleotiden wird durch dieses Reagens desintegriert. Die Ergebnisse wurden im Zusammenhang mit der metabolischen Carcinostasis und der Formulierung des cellulären, Differenzierung und Anomalisation verursachenden Yamafuji-Effekts kurz diskutiert.
    Notes: Summary Three nutritively significant enediol compounds mentioned in above title can inhibit sarcoma-180 growth. The inhibition by ascorbic acid is enhanced by cupric ions. These enediols depolymerize DNA, particularly in co-operation with copper. Dehydroascorbic acid is able to break denatured DNA and to bring about single strand scission for native one. A mixture of dehydroascorbate and Cu decomposes apurinic acid and liberates deoxy-cytidylic acid from it. Only the oligo-form pf pyrimidine tetra- and penta-nucleotides is disintegrated by this reagent. The results were briefly discussed in relation to metabolic carcinostasis and to the formulation of Yamafuji effect causing cellular differentiation and anomalization.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Elastomers, based on cellulose fibers, were synthesized by grafting ethyl acrylate onto fibers preirradiated by a high-energy electron beam. The rheological properties and fine structure of the elastomers were investigated in order to determine factors in development of rubber-like elastomeric behavior. Mechanical properties of the elastomers depended on (1) degree of polymerization of irradiated cellulose molecules, (2) extent of grafting, and (3) experimental methods of evaluation, particularly in varying environmental conditions, for example, in making measurements in air, water, or ethyl acetate. Glass transition temperatures of the elastomers were dependent on the environmental conditions of evaluation; stiffnesses of the elastomers levelled off at about 0°C; and in all environments, a rubber-like plateau was observed. Poly(ethyl acrylate) separated from the elastomers was not soluble in acetone. The mean molecular weight of the separated poly(ethyl acrylate) of the elastomer was determined in ethyl acetate by the equilibrium swelling method. It was concluded that crosslinks existed in the elastomers. Electron microphotographs of cross sections of the elastomers, which exhibited rubber-like behavior, indicated that the fibrillar structure of the irradiated cellulose fibers formed a uniform network and that poly(ethyl acrylate) was uniformly distributed among the fibrils.
    Additional Material: 19 Ill.
    Type of Medium: Electronic Resource
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