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  • 1970-1974  (2)
  • 1935-1939
  • Enzymprotein  (1)
  • Lesch-Nyhan-Syndrom  (1)
  • Purine biosynthesis  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular medicine 50 (1972), S. 1015-1016 
    ISSN: 1432-1440
    Keywords: Enzyme activities (A-PRT) ; (HG-PRT) ; Uricosuric drugs ; Purine biosynthesis ; Gout ; Gichtpatienten ; Uricosuria ; Purinsynthese ; Enzym-Aktivität (A-PRT) und (HG-PRT)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung Es konnte gezeigt werden, daß Benziodaron neben der bereits bekannten uricosurischen Wirkung auch einen direkten Einfluß auf die Purinsynthese hat. Unter der Therapie von Benziodaron kommt es zu einer Aktivitätssteigerung der Adenin- (A-PRT) und der Hypoxanthin-Guanin-Phosphoribosyltransferase (HG-PRT).
    Notes: Summary Benziodaron, a potent uricosuric drug, also influences the biosynthesis of purines. Following Benziodaron administration the activities of adenine- (A-PRT) and hypoxanthine-guanine-phosphoribosyltransferase (HG-PRT) are increased.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular medicine 51 (1973), S. 88-89 
    ISSN: 1432-1440
    Keywords: Lesch-Nyhan Syndrome ; Hypoxanthine-Guanine-Phosphoribosyl transferase enzym protein ; Lesch-Nyhan-Syndrom ; Hypoxanthin-Guanin-Phosphoribosyltransferase ; Enzymprotein
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung Bei 2 Fällen von Lesch-Nyhan-Syndrom mit vollständigem bzw. teilweisem Fehlen der Hypoxanthin-Guanin-Phosphoribosyltransferase-Aktivität konnte Enzymprotein mit einem gegen normales Erythrocytenenzym gerichteten Anti-Serum nachgewiesen werden. Der Defekt dieser angeborenen Stoffwechselerkrankung scheint demnach in der Synthese eines inaktiven, sich im Doppeldiffusionstest immunologisch normal verhaltenden Enzymproteins zu liegen.
    Notes: Summary In two cases of Lesch-Nyhan syndrome with complete and partial deficiency of hypoxanthine-guanine phosphoribosyl transferase activity, the presence of enzyme protein could be demonstrated using a specific antiserum against hypoxanthine-guanine phosphoribosyl transferase from normal erythrocyte. Therefore, the defect in this disease seems to be based on the synthesis of an inactive but in the double-diffusion-technique immunologically normal enzyme protein.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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