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  • Nannochloropsis  (1)
  • Parkinsonism  (1)
  • Springer  (2)
  • American Association for the Advancement of Science
  • American Journal of Science
  • American Society of Hematology
  • 1995-1999
  • 1985-1989  (2)
  • 1980-1984
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  • 1989  (2)
  • 1984
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  • Springer  (2)
  • American Association for the Advancement of Science
  • American Journal of Science
  • American Society of Hematology
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  • 1995-1999
  • 1985-1989  (2)
  • 1980-1984
  • 1975-1979
  • 1965-1969
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  • 1989  (2)
  • 1984
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Planta 178 (1989), S. 450-455 
    ISSN: 1432-2048
    Keywords: Carbon, inorganic (transport) ; Carbonic anhydrase ; Marine microalgae ; Monallantus ; Nannochloropsis ; Stichococcus
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Inorganic-carbon transport was investigated in the eukaryotic marine microalgaeStichococcus minor, Nannochloropsis oculata and aMonallantus sp. Photosynthetic O2 evolution at constant inorganic-carbon concentration but varying pH showed thatS. minor had a greater capacity for CO2 rather than HCO 3 − utilization but forN. oculata andMonallantus HCO 3 − was the preferred source of inorganic carbon. All three microalgae had a low affinity for CO2 as shown by the measurement of inorganic-carbon-dependent photosynthetic O2 evolution at pH 5.0. At pH 8.3, where HCO 3 − is the predominant form of inorganic carbon, the concentration of inorganic carbon required for half-maximal rate of photosynthetic O2 evolution [K 0.5 (CO2)] was 53 μM forMonallantus sp. and 125 μM forN. oculata, values compatible with HCO 3 − transport. Neither extra- nor intracellular carbonic anhydrase was detected in these three microalgal species. It is concluded that these microalgae lack a specific transport system for CO2 but that HCO 3 − transport occurs inN. oculata andMonallantus, and in the absence of intracellular carbonic anhydrase the conversion of HCO 3 − to CO2 may be facilitated by the internal pH of the cell.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    European journal of clinical pharmacology 37 (1989), S. 391-393 
    ISSN: 1432-1041
    Keywords: Parkinsonism ; acetylator phenotype ; sulphamethazine ; debrisoquine oxidation ; drug polymorphism
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary Acetylator phenotype has been determined using sulphamethazine in 100 patients with Parkinson's disease and in 93 age-matched normal control subjects. Sixty-nine patients and 54 control subjects were classified as slow acetylators (NS). No relation was found among acetylator polymorphism and age at onset or clinical stage of disease. Amongst slow acetylators, the percentage of acetylated sulphamethazine in plasma was significantly lower in patients than in controls. Despite this finding, the results do not support any relationship between acetylator polymorphism and the risk of developing Parkinson's disease.
    Type of Medium: Electronic Resource
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