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Titlebook: Calcium in Drug Actions; Peter F. Baker (Professor Sc. D., F.R.S.) Book 1988 Springer-Verlag Berlin Heidelberg 1988 ATP.ATPase.Calcium.bon

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https://doi.org/10.1007/978-3-662-41505-4er pointed out that most cells would accumulate calcium if this was dependent only upon the Donnan ratio. Further with intracellular potentials of around — 60 mV and an external calcium concentration of 1–10 m., intracellular concentrations of 0.1–1.0 . could be expected. Clearly this was not the ca
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Rolf Dornberger,Dino Schwafertstionally, the recent discovery of compounds closely related in structure to the 1,4-dihydro-pyridine, nifedipine, but which serve as Ca. channel activators (Fig. 2) serves to suggest that major new categories of uses ranging from inotropy to secretory stimulation may become available in the future.
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Pascal D. König,Sebastian Jäcklet (C. and M. 1977; G. et al. 1978). This approach has confirmed that the active site of apamin comprises the two residues Arg-13 and Arg-14. The exact three-dimensional structure of the toxin remains unknown. However, recent solution analysis of apamin by NMR techniques has suggested that the toxin
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https://doi.org/10.1007/978-3-322-99733-3evels according to the regulatory requirements of oxidative metabolism. The capacity for Ca. accumulation is also constrained by the tolerance of mitochondrial function to increased Ca. load. It is important to stress that there are therefore two aspects to the behaviour of mitochondria with respect
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https://doi.org/10.1007/978-3-662-25270-3e term exocytosis has expanded to include not only the release, but also the preceding fusion-fission steps. Such an extended meaning is used throughout this chapter (. 1975; . and . 1980 a; . and . 1981).
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0171-2004 ts grateful appreciation for the admirable way in which Professor Baker took on and carried out the additional work of bringing this fine book into existence; a978-3-642-71808-3978-3-642-71806-9Series ISSN 0171-2004 Series E-ISSN 1865-0325
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