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  • Acrylamide Gel Disc Electrophoresis  (1)
  • Chromatin core particles  (1)
  • Glucose-6-phosphate dehydrogenase  (1)
  • Growth hormone  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    International Journal of Biological Macromolecules 5 (1983), S. 130-134 
    ISSN: 0141-8130
    Keywords: Chromatin core particles ; conformational change ; electrophoretic light scattering ; quasi-elastic light scattering
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-1076
    Keywords: Key words Hyperbilirubinemia ; Neonatal jaundice ; Glucose-6-phosphate dehydrogenase
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The pathogenesis of neonatal hyperbilirubinemia has not yet been completely defined in normal and glucose-6-phosphate-dehydrogenase (G6PD)-deficient newborns. The recent identification of a variant promoter in the gene encoding for the bilirubin uridine-diphosphoglucuronosyl-transferase (UGT-1 A) associated with Gilbert's syndrome, allowed us to explore whether the presence of this variant promoter is a risk factor for the development of neonatal hyperbilirubinemia in normal newborns and in association with G6PD deficiency. We found that the variant (TA)7/(TA)7 promoter shows no statistically significant difference in normal or G6PD-deficient newborns developing severe hyperbilirubinemia and in control subjects from the same population. This finding indicates that the variant promoter of UGT-1 A does not contribute to the development of hyperbilirubinemia in the newborn.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    European journal of pediatrics 113 (1972), S. 289-296 
    ISSN: 1432-1076
    Keywords: Serum Alkaline Phosphatase ; Acrylamide Gel Disc Electrophoresis ; L-phenylalanine Inhibition ; L-Homoarginine Inhibition ; Neuraminidase Sensitivity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung In 364 Seren von Neugeborenen (Nabelschnurblut), Säuglingen, Kindern und Erwachsenen wurde die vorhandene alkalische Phosphatase genauer differenziert unter Anwendung der L-Phenylalaninhemmung, der L-Homoargininhemmung, der Hitzedenaturierung, der Arcylamidgel-Scheibenelektrophorese und der Neuramidaseempfindlichkeit. Die hohen Werte der alkalischen Phosphatase im Nabelschnur-, Säuglings-und Kinderserum im Vergleich zu den Erwachsenenwerten werden mehr den Phosphatasen der Knochen als den intestinalen Phosphatasen zugerechnet. Mit Hilfe der Acrylgelelektrophorese konnte eine Zunahme der intestinalen alkalischen Phosphatase mit steigendem Lebensalter nachgewiesen werden.
    Notes: Abstract In 364 serum samples of cord blood, infants, children, and adults alkaline phosphatase was characterized by means of L-phenylalanine inhibition, L-homoarginine inhibition, heat inactivation, acrylamide gel disc electrophoresis, and neuraminidase sensitivity. The increase of serum alkaline phosphatase in cord blood serum and in infant's and children's serum in comparison with adult levels was attributed mainly to the bone enzyme and in smaller proportion to the intestinal enzyme. Using acrylamide gel disc electrophoresis, an increase in the frequency of subjects with an intestinal alkaline phosphatase band with increasing age values was found.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    European journal of pediatrics 153 (1994), S. 110-112 
    ISSN: 1432-1076
    Keywords: Growth hormone ; Hypothalamus ; Ring chromosome ; Short stature
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract We report on a boy with a ring 18 chromosome associated with hypothalamic growth hormone (GH) deficiency. A 12-month trial of GH replacement therapy (0.5 U/kg/week) resulted in a marked growth acceleration. Our findings emphasise the need of evaluating GH secretion in patients with abnormalities of the 18 chromosome.
    Type of Medium: Electronic Resource
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