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  • Key words Glycogen storage disease type Ia  (1)
  • Polyurethaneionomer  (1)
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  • 1
    Digitale Medien
    Digitale Medien
    Springer
    Colloid & polymer science 270 (1992), S. 956-961 
    ISSN: 1435-1536
    Schlagwort(e): Polyurethaneionomer ; DMPA ; neutralization ; mechanicalproperties ; viscoelasticproperties
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie , Maschinenbau
    Notizen: Abstract Polyurethane (PU) ionomers were prepared using various types of polyol (PTAd, PCL, PTMG, and PPG) and isocyanate (MDI, HDI, and IPDI), together with different extender (DMPA) contents, degree of neutralization, and number average molecular weight (M n) of polyol. Modulus (E′), strength (σb), and glass transition temperature (T g) significantly increased with the increased amount of extender and extender neutralization. Among three of the iocyanate used, PU from MDI gave the highest modulus, strength, andT g. With regard to theM n of PTAd (600, 1000, 2000), PU from PTAd 600M n gave the highest modulus, strength, andT g, due probably to the highest hard segment content and phase mixing. On the other hand, PU from PTAd 2000M n gave significantly improved strength over PTAd 1000M n, and the highest elongation. The results were interpreted in terms of soft-segment crystallization, and soft-hard phase separation, which was concluded from the lowered softT g.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 2
    ISSN: 1435-232X
    Schlagwort(e): Key words Glycogen storage disease type Ia ; Glucose-6-phosphatase ; Mutation ; Chinese ; Taiwan
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie , Medizin
    Notizen: Abstract Glycogen storage disease type Ia (GSD Ia) is caused by a deficiency of glucose-6-phosphatase (G6Pase) activity. Eighteen GSD Ia families were studied for G6Pase gene mutations. Thirty-two mutations were found in 36 GSD Ia chromosomes: 16 were 727 G→T (44.44%); 13 were R83H (327 G→T; 36.11%); 1 was 341delG; 1 was 933insAA; and 1 was 793 G→T. The 727 G→T and R83H mutations together accounted for 80.56% (29/36) of the GSD Ia chromosomes. These two mutations were easily examined by polymerase chain reaction-based methods, and the prenatal diagnosis of a non-affected fetus was successfully made. The 727 G→T mutation is the predominant mutation in Japanese GSD Ia patients, but is rarely seen in Western counties. The 727 G→T mutation is also the most prevalent mutation in Taiwan Chinese, although the incidence is not as high as in Japan.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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