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  • Articles: DFG German National Licenses  (2)
  • 1995-1999  (2)
  • 1965-1969
  • Key words XYY syndrome  (1)
  • Key words Carboxyl group  (1)
  • Prader-Willi syndrome  (1)
  • 1
    ISSN: 1435-1536
    Keywords: Key words Carboxyl group ; emulsion polymerization ; nanoparticles ; microsphere ; emulsifier
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract  Styrene-methacrylic acid copolymer (P(S-MAA)) nanoparticles having high Tg were produced by a dissolution of submicron-sized P(S-MAA) particles as follows. Submicron-sized P(S-MAA) particles having various MAA contents were produced by emulsion copolymerization. Secondly, they were treated in a polyoxyethylene nonylphenyl-ether nonionic emulsifier aqueous solution at pH 13.0 and above 90 °C. The nanoparticles having about 30 nm in diameter were only produced from the particles having MAA contents around 7 mol%, and above the contents, they were not produced. It seems to be based on that emulsifier molecules are not adsorbed onto the polymer molecules enough to dissolve them. The effect of MAA content on such a dissolution behavior was examined using seven kinds of different nonionic emulsifiers having hydrophile-lipophile-balance values between 12.2 and 18.2 at various temperatures and initial pH.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of human genetics 44 (1999), S. 412-413 
    ISSN: 1435-232X
    Keywords: Key words XYY syndrome ; Prader-Willi syndrome ; Uniparental maternal disomy ; Non-disjunction of chromosome
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract We report a 26-month-old boy with XYY syndrome, with the complication of Prader-Willi syndrome (PWS) due to uniparental maternal disomy of chromosome 15. To our knowledge, this is the first case of XYY syndrome and PWS. Clinical findings were fully compatible with the diagnostic criteria for PWS. Molecular analysis revealed a maternal heterodisomy of chromosome 15, indicating that non-disjunction of chromosome 15 had occurred at maternal meiosis I, and that the non-disjunction of chromosome Y and of chromosome 15 had occurred independently.
    Type of Medium: Electronic Resource
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