Titlebook: Basic Aspects of Receptor Biochemistry; Proceedings of the I Menek Goldstein,Kurt Jellinger,Peter Riederer Conference proceedings 1983 Spri

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强行引入

Eichendorff, Heidelberg und die Blaue Blumeiature end-plate current, .. the action of a quantum if nerve-released acetylcholine (ACh), by 50%. On the other hand, drugs that interfere with receptor function without preventing ACh binding to receptors can be just as (or more) effective in blocking nerve-applied as in blocking exogenously appli

亲密

https://doi.org/10.1007/978-3-642-46021-0t from the antiporter of heart mitochondria. These results are discussed in terms of Ca.-binding proteins being potential targets for pharmacological interventions designed to block specific aspects of the action of calcium.

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Das Diakoniewissenschaftliche Institutological responsiveness of NE receptor systems, the number of receptors and the efficacy of their coupling to adenylate cyclase appear to represent control mechanisms for the intensity of signal transfer.

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Richard Rothes Berufung Nach Heidelberg 1837nylate cyclase activity; apomorphine, a dopaminergic agonist, abolishes this effect of GTP. It is hypothesized that the D-2 dopamine receptor in the IL interacts with an inhibitory guanyl nucleotide component (N.); stimulation of the D-2 dopamine receptor alters the properties of N. so that N. can i

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Wie das Bild der Atomkerne Sichtbar wurde,st unchanged. When mice are treated for 12 days with neuroleptics, supersensitivity to methylphenidate is induced. The supersensitivity is reversed by thioxanthenes, whereas butyrophenones and diphenylbutylpiperidines have no effect at all. These differenes do not appear to be due to a change in the