Farmakologija

Reference

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10. ↑^10,010,1Peroutka SJ (May 1988). „Antimigraine drug interactions with serotonin receptor subtypes in human brain”. Annals of Neurology 23 (5): 500–4. DOI:10.1002/ana.410230512. PMID 2898916. 
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13. ↑^{13,013,113,213,313,4}Toll L, Berzetei-Gurske IP, Polgar WE,et al. (March 1998). „Standard binding and functional assays related to medications development division testing for potential cocaine and opiate narcotic treatment medications”. NIDA Research Monograph 178: 440–66. PMID 9686407. 
14. ↑^14,014,1F. S. Dukhovich (15. 8. 2005.). Pharmacological aspects of molecular recognition. Nova Publishers. str. 117. ISBN 978-1-59454-676-1. Pristupljeno 27 November 2011. 
15. ↑Kohen R, Metcalf MA, Khan N,et al. (January 1996). „Cloning, characterization, and chromosomal localization of a human 5-HT6 serotonin receptor”. Journal of Neurochemistry 66 (1): 47–56. DOI:10.1046/j.1471-4159.1996.66010047.x. PMID 8522988. 
16. ↑^16,016,1Bard JA, Zgombick J, Adham N, Vaysse P, Branchek TA, Weinshank RL (November 1993). „Cloning of a novel human serotonin receptor (5-HT7) positively linked to adenylate cyclase”. The Journal of Biological Chemistry 268 (31): 23422–6. PMID 8226867. ^{[mrtav link]}
17. ↑Hoyer D, Neijt HC (March 1988). „Identification of serotonin 5-HT3 recognition sites in membranes of N1E-115 neuroblastoma cells by radioligand binding”. Molecular Pharmacology 33 (3): 303–9. PMID 3352595. ^{[mrtav link]}
18. ↑Runyon SP, Savage JE, Taroua M, Roth BL, Glennon RA, Westkaemper RB (March 2001). „Influence of chain length and N-alkylation on the selective serotonin receptor ligand 9-(aminomethyl)-9,10-dihydroanthracene”. Bioorganic & Medicinal Chemistry Letters 11 (5): 655–8. DOI:10.1016/S0960-894X(01)00023-3. PMID 11266163. 
19. ↑Lowe DA, Matthews EK, Richardson BP (November 1981). „The calcium antagonistic effects of cyproheptadine on contraction, membrane electrical events and calcium influx in the guinea-pig taenia coli”. British Journal of Pharmacology 74 (3): 651–63. PMC 2071752. PMID 6271323. 
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