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5-HT7 receptor (Serbo-Croatian Wikipedia)

Analysis of information sources in references of the Wikipedia article "5-HT7 receptor" in Serbo-Croatian language version.

refsWebsite
Global rank Serbo-Croatian rank
23nih.gov
4th place
3rd place
21doi.org
2nd place
2nd place
1archive.org
6th place
5th place

archive.org

doi.org

dx.doi.org

nih.gov

ncbi.nlm.nih.gov

  • Vanhoenacker P, Haegeman G, Leysen JE (February 2000). „5-HT7 receptors: current knowledge and future prospects”. Trends Pharmacol. Sci. 21 (2): 70–7. DOI:10.1016/S0165-6147(99)01432-7. PMID 10664612. 
  • Ruat M, Traiffort E, Leurs R, Tardivel-Lacombe J, Diaz J, Arrang JM, Schwartz JC (September 1993). „Molecular cloning, characterization, and localization of a high-affinity serotonin receptor (5-HT7) activating cAMP formation”. Proc. Natl. Acad. Sci. U.S.A. 90 (18): 8547–51. DOI:10.1073/pnas.90.18.8547. PMC 47394. PMID 8397408. 
  • Bard 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”. J. Biol. Chem. 268 (31): 23422–6. PMID 8226867. 
  • Mnie-Filali O, Lambás-Señas L, Zimmer L, Haddjeri N (December 2007). „5-HT7 receptor antagonists as a new class of antidepressants”. Drug News Perspect. 20 (10): 613–8. DOI:10.1358/dnp.2007.20.10.1181354. PMID 18301795. 
  • Heidmann DE, Metcalf MA, Kohen R, Hamblin MW (April 1997). „Four 5-hydroxytryptamine7 (5-HT7) receptor isoforms in human and rat produced by alternative splicing: species differences due to altered intron-exon organization”. J. Neurochem. 68 (4): 1372–81. DOI:10.1046/j.1471-4159.1997.68041372.x. PMID 9084407. 
  • Hedlund PB, Sutcliffe JG (September 2004). „Functional, molecular and pharmacological advances in 5-HT7 receptor research”. Trends Pharmacol. Sci. 25 (9): 481–6. DOI:10.1016/j.tips.2004.07.002. PMID 15559250. 
  • Sprouse J, Reynolds L, Li X, Braselton J, Schmidt A (2004). „8-OH-DPAT as a 5-HT7 agonist: phase shifts of the circadian biological clock through increases in cAMP production”. Neuropharmacology 46 (1): 52–62. DOI:10.1016/j.neuropharm.2003.08.007. PMID 14654097. 
  • Powell SL, Gödecke T, Nikolic D, Chen SN, Ahn S, Dietz B, Farnsworth NR, van Breemen RB, Lankin DC, Pauli GF, Bolton JL (2008). „In vitro serotonergic activity of black cohosh and identification of N(omega)-methylserotonin as a potential active constituent”. J Agric Food Chem 56 (24): 1718–1726. DOI:10.1021/jf803298z. PMID 19049296. 
  • Leopoldo M, Lacivita E, Contino M, Colabufo NA, Berardi F, Perrone R (2007). „Structure-activity relationship study on N-(1,2,3,4-tetrahydronaphthalen-1-yl)-4-aryl-1-piperazinehexanamides, a class of 5-HT7 receptor agents. 2”. J. Med. Chem. 50 (17): 4214–21. DOI:10.1021/jm070487n. PMID 17649988. 
  • Leopoldo M, Berardi F, Colabufo NA, et al. (2004). „Structure-affinity relationship study on N-(1,2,3,4-tetrahydronaphthalen-1-yl)-4-aryl-1-piperazinealkylamides, a new class of 5-hydroxytryptamine7 receptor agents”. J. Med. Chem. 47 (26): 6616–24. DOI:10.1021/jm049702f. PMID 15588097. 
  • Pittalà V, Salerno L, Modica M, Siracusa MA, Romeo G (2007). „5-HT7 receptor ligands: recent developments and potential therapeutic applications”. Mini Rev Med Chem 7 (9): 945–60. DOI:10.2174/138955707781662663. PMID 17897083. 
  • Leopoldo M (2004). „Serotonin(7) receptors (5-HT(7)Rs) and their ligands”. Curr. Med. Chem. 11 (5): 629–61. DOI:10.2174/0929867043455828. PMID 15032609. 
  • Krobert KA and Levy FO (2002) The human 5-HT7 serotonin receptor splice variants: constitutive activity and inverse agonist effects. Br J Pharmacol 135(6):1563-1571. (2002). „The human 5-HT7 serotonin receptor splice variants: constitutive activity and inverse agonist effects.”. British journal of pharmacology 135 (6): 1563–71. DOI:10.1038/sj.bjp.0704588. PMC 1573253. PMID 11906971. 
  • Volk B, Barkóczy J, Hegedus E, et al. (April 2008). „(Phenylpiperazinyl-butyl)oxindoles as selective 5-HT7 receptor antagonists”. J. Med. Chem. 51 (8): 2522–32. DOI:10.1021/jm070279v. PMID 18361484. 
  • Abbas AI, Hedlund PB, Huang XP, Tran TB, Meltzer HY, Roth BL (July 2009). „Amisulpride is a potent 5-HT7 antagonist: relevance for antidepressant actions in vivo”. Psychopharmacology (Berl.) 205 (1): 119–28. DOI:10.1007/s00213-009-1521-8. PMC 2821721. PMID 19337725. 
  • Romero G, Pujol M, Pauwels PJ (2006). „Reanalysis of constitutively active rat and human 5-HT7(a) receptors in HEK-293F cells demonstrates lack of silent properties for reported neutral antagonists”. Naunyn Schmiedebergs Arch. Pharmacol. 374 (1): 31–9. DOI:10.1007/s00210-006-0093-y. PMID 16967291. 
  • Forbes IT, Dabbs S, Duckworth DM, et al. (February 1998). „(R)-3,N-dimethyl-N-[1-methyl-3-(4-methyl-piperidin-1-yl) propyl]benzenesulfonamide: the first selective 5-HT7 receptor antagonist”. J. Med. Chem. 41 (5): 655–7. DOI:10.1021/jm970519e. PMID 9513592. 
  • Mahé C, Loetscher E, Feuerbach D, Müller W, Seiler MP, Schoeffter P (2004). „Differential inverse agonist efficacies of SB-258719, SB-258741 and SB-269970 at human recombinant serotonin 5-HT7 receptors”. Eur. J. Pharmacol. 495 (2-3): 97–102. DOI:10.1016/j.ejphar.2004.05.033. PMID 15249157. 
  • Lovell PJ, Bromidge SM, Dabbs S, Duckworth DM, Forbes IT, Jennings AJ, King FD, Middlemiss DN, Rahman SK, Saunders DV, Collin LL, Hagan JJ, Riley GJ and Thomas DR (2000) A novel, potent, and selective 5-HT(7) antagonist: (R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolidine-1-sulfonyl) phen ol (SB-269970). J Med Chem 43(3):342-345. (2000). „A novel, potent, and selective 5-HT(7) antagonist: (R)-3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolidine-1-sulfonyl) phen ol (SB-269970).”. Journal of medicinal chemistry 43 (3): 342–5. DOI:10.1021/jm991151j. PMID 10669560. 
  • Forbes IT, Douglas S, Gribble AD, et al. (November 2002). „SB-656104-A: a novel 5-HT(7) receptor antagonist with improved in vivo properties”. Bioorg. Med. Chem. Lett. 12 (22): 3341–4. DOI:10.1016/S0960-894X(02)00690-X. PMID 12392747. 
  • Zhang J, Ferguson SS, Barak LS, Aber MJ, Giros B, Lefkowitz RJ and Caron MG (1997) Molecular mechanisms of G protein-coupled receptor signaling: role of G protein-coupled receptor kinases and arrestins in receptor desensitization and resensitization. Receptors Channels 5(3-4):193-199. (1997). „Molecular mechanisms of G protein-coupled receptor signaling: role of G protein-coupled receptor kinases and arrestins in receptor desensitization and resensitization.”. Receptors & channels 5 (3-4): 193–9. PMID 9606723. 
  • Smith C, Rahman T, Toohey N, Mazurkiewicz J, Herrick-Davis K and Teitler M (2006) Risperidone irreversibly binds to and inactivates the h5-HT7 serotonin receptor. Mol Pharmacol 70(4):1264-1270. (2006). „Risperidone irreversibly binds to and inactivates the h5-HT7 serotonin receptor.”. Molecular pharmacology 70 (4): 1264–70. DOI:10.1124/mol.106.024612. PMID 16870886. 
  • Knight JA, Smith C, Toohey N, Klein MT and Teitler M (2009) Pharmacological analysis of the novel, rapid, and potent inactivation of the human 5-Hydroxytryptamine7 receptor by risperidone, 9-OH-Risperidone, and other inactivating antagonists. Mol Pharmacol 75(2):374-380. (2009). „Pharmacological analysis of the novel, rapid, and potent inactivation of the human 5-Hydroxytryptamine7 receptor by risperidone, 9-OH-Risperidone, and other inactivating antagonists.”. Molecular pharmacology 75 (2): 374–80. DOI:10.1124/mol.108.052084. PMC 2671286. PMID 18996971.