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Titlebook: Clinical Pharmacology in Psychiatry; Strategies in Psycho Lars F. Gram,Luc P. Balant,Svein G. Dahl Conference proceedings 1993 Springer-Ver

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發(fā)表于 2025-3-25 04:27:29 | 只看該作者
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發(fā)表于 2025-3-25 13:26:35 | 只看該作者
Evaluation of Existing Fragility Curves, with intra- and extracellular loops of various lengths, and (c) a COOH-terminal intracellular domain often containing several sites for phosphorylation by protein kinases (O’Dowd et al. 1989; Strosberg 1991; Strosberg and Leysen 1991).
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發(fā)表于 2025-3-25 17:59:23 | 只看該作者
https://doi.org/10.1007/978-3-319-47479-3in linked receptors; the 5-HT. (DeVivo and Maayani 1985), 5-HT. (Ariani et al. 1989), and 5-HT. (Peroutka 1988) receptors are coupled to adenylyl cyclase inhibitory (G.) proteins, while the 5-HT. receptor is coupled to phospholipase C through a Gp protein (Conn et al. 1986).
25#
發(fā)表于 2025-3-25 22:23:14 | 只看該作者
About Liberal Democracy and Extremism,ts and antagonists directed at certain 5-HT receptor classes and subclasses. Some of these drugs are considered as potentially useful for the treatment of psychiatric disorders, for example, 5-HT. receptor agonists, which act as anxiolytics and antidepressants, and 5-HT. receptor antagonists, which appear to possess antipsychotic properties.
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發(fā)表于 2025-3-26 16:00:31 | 只看該作者
https://doi.org/10.1007/978-94-007-7872-6 receptor (Sylte et al., to be published), and the 5-HT. receptor (Edvardsen et al. 1992), based on their amino acid sequence. The models were constructed by computer graphics and molecular modeling techniques, and used to examine the mechanisms of drug and neurotransmitter interactions with these receptors.
30#
發(fā)表于 2025-3-26 18:29:27 | 只看該作者
Reform and Transition in the Mediterraneann or suspected subtypes - 5-HT., 5-HT., 5-HT. and 5-HT. - still remain to be cloned. At least one of these, the 5-HT. receptor(s), is a member of the multisubunit ligand-gated ion channel superfamily and likely to be unrelated in structure to the 7TM receptors known at this time.
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