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  • 1970-1974  (5)
  • Polymer and Materials Science  (3)
  • Cell & Developmental Biology  (2)
  • Evolution
  • Mitochondria
  • glycosylation
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  • 1
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Adult newts placed in an atmospheric environment of 85% oxygen, saturated humidity, and at a temperature of 20 ± 1°C survived particularly well a 44-day test period. They did not succumb to “oxygen toxicity” as has been frequently reported for other vertebrate species.Having established the newt's tolerance of high oxygen atmosphere, the effect of oxygen on growth and development in the regenerating newt limb was investigated. Under the atmospheric conditions described above, and under 92% oxygen, the regeneration of adult newt limbs appeared to be retarded during the first 25 days after amputation when compared with regenerating limbs of control animals kept under a normal atmosphere of 21% oxygen (air). Thereafter, little or no difference could be discerned between the regeneration of experimental and control limbs.It is known that molecular oxygen participates directly in the hydroxylation of proline to hydroxyproline in the synthesis of collagen. Sectioned regenerates stained specifically for collagen were examined to determine if collagen synthesis was induced in experimental animals. Two regeneration-inhibited limbs of oxygenated newts showed cicatrical repair of the apical limb stump 25 days after amputation. However, the majority of the experimental animals revealed no obvious increase in collagen fibers.These results contraindicate any marked “oxygen toxicity” affecting the life of the newts, or regeneration of their limbs. It is suggested that a change in collagen fiber type might have been induced by the high-oxygen atmosphere. Investigations to test this hypothesis are currently underway.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 15 (1971), S. 3053-3066 
    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: Various substituted difunctional 1,3-dioxolanes and 1,3-dioxanes were copolymerized with a cyclic vinyl ether, 3,4-dihydro-2H-pyran-2-methyl(3,4-dihydro-2H-pyran-2-carboxylate), in the presence of boron trifluoride etherate catalyst. The copolymerizations proceeded rapidly and exothermally when initiated at room temperature and produced thermosetting resins. The copolymer products possess improved abrasion resistance and toughness as compared with homopolymer of the di(dihydropyranyl) monomer. As a practical consequence of these copolymerizations it is possible to prepare low-density pyranyl rigid foams with improved friability resistance.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 16 (1972), S. 2361-2373 
    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: The role of mixtures of reactive bromine and phosphorus flame-retardant polyol intermediates as well as the individual bromine and phosphorus reagents in suppressing combustion of flexible polyurethane foams was investigated by means of the oxygen index flame test and charring techniques. Bromine alone appears to contribute to flame retardancy in the solid as well as the vapor phase. A substantial portion of the bromine from both aliphatic and aromatic bromide flame retardants was accounted for in the char, and this is also true when phosphorus is present. Ionic bromine appears to be the most effective elemental form. Like phosphorus, bromine alone in foams is also observed to increase the yield of char. Aliphatic bromide in mixture with phosphonate or phosphate gave enhanced flame retardancy, whereas, mixtures with phosphite are not beneficial. Maximum flame retardancy and char yields correlate well for bromine mixed with phosphate and phosphonate, whereas the relationship does not hold with phosphites. Charring experiments at 500°C with foams containing both phosphorus and bromine generally afforded a constant P/Br ratio, suggesting a specific chemical interaction for flame retardancy. Phosphate flame-retardant efficiency was sensitive to concentration of phosphorus in the foams. On the other hand, phosphonate and phosphite exhibited a constant level of fire resistance at phosphorus levels greater than 0.3%.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 17 (1973), S. 2463-2483 
    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: A chemical model is outlined which gives a simple description of flame-retardant efficiency of organic bromides in flexible polyurethane foam systems. The mechanism suggests dehydrobromination by an interplay of SN1 and SN2 reactions in intramolecular and intermolecular processes. Evidence is presented to demonstrate that flame-retardant efficiency is directly related to the facility of dehydrohalogenation by an intramolecular process in which cyclic urethanes (five to ten membered rings) are formed by either SN1 and/or SN2 reactions. The requirement for a nucleophile, such as carbamate nitrogen, in halogen systems is suggested. In other mechanistic aspects, it was shown that flame retardancy passes through a maximum as a function of bromide content in the foam. It is believed that this behavior reflects certain undefined combustion aspects in the solid phase. It is also shown that unlike additive flame retardants, the TGA's of neither the starting bromine-containing alcohols nor their model N-phenylcarbamates correlate with the weight loss curves of the control foam. Instead, the TGA's of both flame retardant and nonflame-retarded foams from the reactive bromide alcohols all fall in about the decomposition range of the control foam. As a practical consequence of the results reported herein, it is now possible to correlate flame retardancy and structure as well as formulate new flame retardants with greater assurance of success.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Cellular Physiology 76 (1970), S. 253-263 
    ISSN: 0021-9541
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Naturally occurring defective phage particles, which do not form plaques on any known host, but have a restricted host killing range, appear to be widely distributed. The defective phages are produced spontaneously but can be induced, at much higher levels, by chemical and physical agents which interfere with metabolism or structure of DNA. The defective phages discussed in this article have been divided into various categories on the basis of their structural complexity, which ranges from what appears to be phage tail components through to intact phage particles, and the source of the DNA packaged into the heads of the phage-like particles. The evolution of the defective phages is discussed and the possibility is entertained that they may have originated from temperate phages.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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