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  • 1
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 213 (1967), S. 180-181 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Some of the inherent limitations of the technique which employs slices can be overcome by the use of fragments of tubules6. In such a preparation the destruction of tubular architecture causes the exposure of luminal cell membranes to the incubation medium. This is illustrated in Fig. 1 which shows ...
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 161 (1948), S. 131-132 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] IN a recent communication in Nature1, Dr. P. George described manometric experiments which showed a rapid initial decay of the enzyme compared with which the well-known decay due to irreversible destruction was so slow that the rate became almost steady. These experiments were ...
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 175 (1955), S. 87-88 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Excess coenzyme does not inhibit the increased citrate oxidation in the presence of aspartate (aspart-ate reaction). This clearly distinguishes the effect of aspartate in yeast from the effect in certain mammalian systems where aspartate can be shown to accelerate citrate oxidation by increasing ...
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Pflügers Archiv 360 (1975), S. 1-6 
    ISSN: 1432-2013
    Keywords: Peritubular Membrane ; Luminal Membrane ; Urate Permeability ; Urate Secretion ; Rat Kidney ; PAH
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Measurement in the rat of renal artery-to-vein transit times permitted evaluation of movement of14C-labelled urate and of other solutes out of the peritubular inulin spaces in the renal cortex. No interaction between urate and PAH could be demonstrated at this level. Provided the peritubular disappearance may be equated to cellular uptake a mean unidirectional urate flux across peritubular membranes equal to about 1/3 of total renal load may be calculated. This value greatly exceeds the net secretory flux of urate. Such a fact can be explained by the likelihood of significant post-proximal reabsorption of secreted urate, and/or by the conclusion that peritubular urate permeability exceeds that of the luminal side. Assignment of the limiting step in urate secretion to the luminal cell membranes, in contrast to a determining role played by peritubular membranes in PAH transport, can account for the lack of interaction between PAH and urate at the peritubular membrane in rats.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Environmental geochemistry and health 8 (1986), S. 91-94 
    ISSN: 1573-2983
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Medicine
    Notes: Abstract Because renal cortex is a primary target organ of Cd the seriousness of human exposure is commonly assessed in terms of the extent to which it permits renal cortical Cd concentrations to approach a critical value. The critical value has been defined in terms of PCC-10, the population critical concentration at which 10% of exposed individuals may be expected to show abnormal renal function. In chronically exposed human populations, PCC-10 appears to lie in the range of 180 to 220 μg Cd/gram fresh weight of cortex. However, Cd accumulated in the kidney under these conditions is distributed between more than one compartment, in all likelihood differing greatly in their toxicological characteristics. For instance, a major fraction of this Cd is bound to metallothionein, and may as such be relatively inert. Compartmentation of tissue Cd, in turn, is strongly influenced by the nature of exposure, and the PCC-10 value of 200 μg/g may therefore have limited general significance. The problem of risk assessment is further complicated by the high variability of Cd absorption. Nevertheless, human renal Cd levels commonly reach values as high as 1/3 to 1/6 of the chronic PCC-10, and further increases in Cd intake should therefore be avoided.
    Type of Medium: Electronic Resource
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