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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Biochemistry 6 (1967), S. 1348-1360 
    ISSN: 1520-4995
    Source: ACS Legacy Archives
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Chemical reviews 21 (1921), S. 287-297 
    ISSN: 1520-6890
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    The journal of membrane biology 9 (1972), S. 141-154 
    ISSN: 1432-1424
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Summary Acidimetric titration of intact rat liver mitochondria discloses a buffer power of about 45 mEquiv per g between pH 7 and 8, the value rises to 60 mEquiv per g per pH unit after lysis using Triton X-100. The existence and properties of this buffer system have been related to mitochondrial anion accumulation. The uptake of permeant anions by mitochondria occurs to a charge-dependent extent and they are in electrochemical equilibrium with each other and the protons as in a Donnan system. Adding permeant anion causes the intramitochondrial anion content to rise towards a saturation level, the inside to outside concentration ratio falls and concomitantly the transmembrane proton gradient diminishes, making the interior less alkaline. The falling internal pH is associated with protonation of the internal buffer, thus providing a second method for measuring the buffer power, a method which also tests the arguments used in the calculations. The titration curve is constructed by relating the internal pH (deduced from the permeant anion ratio) to the total internal anion equivalents which in turn determines the ionization state of the buffer because the sum of the internal anion equivalents, including the buffer anion, equals the equivalents of internal cation. The buffer power so measured agrees with the acidimetric method applied to lysed mitochondria. The disparity between the acidimetric data from lysed and unlysed mitochondria follows theoretical predictions.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    European radiology 5 (1995), S. 36-42 
    ISSN: 1432-1084
    Keywords: Flow quantitation ; Pedal blood flow ; Peripheral vascular occlusive disease ; Phase contrast MRI
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract This study attempts to evaluate the reliability of cine phase contrast (PC) flow measurements in the assessment of normal pedal blood flow and quantitation of revascularisation-induced flow changes in patients with end-stage peripheral vascular occlusive disease (PVOD). Oblique axial cine-PC acquisitions were obtained on a 1.5 T MRI system at the level of the talotibial joints in 8 normal subjects on four separate occasions. Subsequently 8 patients with end-stage PVOD were examined before and after surgical revascularisation (bilateral, n = 2; unilateral, n = 6). Measured flow in the trifurcation vessels was highly variable among normal subjects. Total pedal flow ranged from 32 to 183 ml/min (mean 91 ml/min) and was significantly different between the subjects evaluated (P 〈 0.0001). Measurements in the same subject over time were considerably less variable (P 〈 0.005). Normal arterial flow patterns were consistently triphasic; those in patients with PVOD were either mono- or biphasic. Pedal flow measured by cine-PC in patients was reduced compared with normal subjects (mean 38.3 ml/min). Flow was slower in symptomatic limbs (26.7 ml/min) compared with asymptomatic ones (48.9 ml/min). Flow increases in revascularised limbs (mean 315%) were significantly different from those observed in non-affected limbs (P 〈 0.005). The ability to quantitate pedal blood flow and subsequent revascularisation-induced flow increases appears promising for the identification of optimal treatment options and monitoring of treatment results.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 179 (1957), S. 1068-1069 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] IF the frog's heart is immersed in solutions of a low calcium-ion concentration (less than 1*5 mM) the resulting weak contractions can be restored to normal by one of the following changes in the ionic environment: (a) by addition of calcium ions, (b) by replacement of part of the sodium ...
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 175 (1955), S. 262-262 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] When this technique is applied to measurement of water permeability of cell walls, the rate of movement per unit difference of concentration of isotopic water is sometimes less by a factor as high as 50 from the rate of movement resulting from a unit difference of water concentration imposed by the ...
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 142 (1938), S. 830-830 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] CONTINUING the investigation on the alkyl peroxides1 and their relation to combustion phenomena, we have now obtained data on ethyl hydrogen peroxide, and propyl hydrogen peroxide. Ethyl hydrogen peroxide decomposes hetero-geneously in the temperature range 140-200°, the ...
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 215 (1967), S. 1487-1488 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Net synthesis of ATP accompanying stimulation of potassium efflux by valinomycin is shown in Fig. 1A. The increase in ATP is accompanied by an equivalent decrease in ADP and a negligible change in AMP. There is thus a net increase in high energy phosphate indicating that the elevation in ATP is not ...
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 213 (1967), S. 1126-1127 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Parallel studies of the metabolic effects of agents which induce ion permeability, such as valinomycin, led to the finding that the maximal respiration attainable on adding an uncoupling agent could be increased by prior induction of a high permeability to potassium ions, with its attendant uptake ...
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Journal of neurochemistry 38 (1982), S. 0 
    ISSN: 1471-4159
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Abstract: The effect of agents that change the respiratory state of the mitochondrion on tyramine oxidation was investigated. Neither uncoupler nor ADP and Pt in the presence of substrate produced any change in the rate of tyramine oxidation, as judged by direct measurement of tyramine oxidation or by H2O2 production. We conclude that previously reported depression of monoamine oxidase activity by stimulated respiration was due to oxygen depletion.
    Type of Medium: Electronic Resource
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