BRL-15572 (Serbian Wikipedia)
Analysis of information sources in references of the Wikipedia article "BRL-15572" in Serbian language version.
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Serbian rank
11th place
23rd place
doi.org
- Price, G. W.; Burton, M. J.; Collin, L. J.; Duckworth, M.; Gaster, L.; Göthert, M.; Jones, B. J.; Roberts, C.; Watson, J. M.; Middlemiss, D. N. (1997). „SB-216641 and BRL-15572--compounds to pharmacologically discriminate h5-HT1B and h5-HT1D receptors”. Naunyn-Schmiedeberg's Archives of Pharmacology. 9303567 (3): 312—320. PMID 9303567. S2CID 26760453. doi:10.1007/pl00005056.
- Schlicker, E.; Fink, K.; Molderings, G. J.; Price, G. W.; Duckworth, M.; Gaster, L.; Middlemiss, D. N.; Zentner, J.; Likungu, J.; Göthert, M. (1997). „Effects of selective h5-HT1B (SB-216641) and h5-HT1D (BRL-15572) receptor ligands on guinea-pig and human 5-HT auto- and heteroreceptors”. Naunyn-Schmiedeberg's Archives of Pharmacology. 9303568 (3): 321—327. PMID 9303568. S2CID 12246022. doi:10.1007/pl00005057.
- Marcoli, M.; Maura, G.; Munari, C.; Ruelle, A.; Raiteri, M. (1999). „Pharmacological diversity between native human 5-HT1B and 5-HT1D receptors sited on different neurons and involved in different functions”. British Journal of Pharmacology. 10188970 (3): 607—612. PMC 1565844
. PMID 10188970. doi:10.1038/sj.bjp.0702336. - Goadsby, P. J.; Classey, J. D. (2003). „Evidence for serotonin (5-HT)1B, 5-HT1D and 5-HT1F receptor inhibitory effects on trigeminal neurons with craniovascular input”. Neuroscience. 14614913 (2): 491—498. PMID 14614913. S2CID 24825348. doi:10.1016/s0306-4522(03)00570-0.
nih.gov
ncbi.nlm.nih.gov
- Price, G. W.; Burton, M. J.; Collin, L. J.; Duckworth, M.; Gaster, L.; Göthert, M.; Jones, B. J.; Roberts, C.; Watson, J. M.; Middlemiss, D. N. (1997). „SB-216641 and BRL-15572--compounds to pharmacologically discriminate h5-HT1B and h5-HT1D receptors”. Naunyn-Schmiedeberg's Archives of Pharmacology. 9303567 (3): 312—320. PMID 9303567. S2CID 26760453. doi:10.1007/pl00005056.
- Schlicker, E.; Fink, K.; Molderings, G. J.; Price, G. W.; Duckworth, M.; Gaster, L.; Middlemiss, D. N.; Zentner, J.; Likungu, J.; Göthert, M. (1997). „Effects of selective h5-HT1B (SB-216641) and h5-HT1D (BRL-15572) receptor ligands on guinea-pig and human 5-HT auto- and heteroreceptors”. Naunyn-Schmiedeberg's Archives of Pharmacology. 9303568 (3): 321—327. PMID 9303568. S2CID 12246022. doi:10.1007/pl00005057.
- Marcoli, M.; Maura, G.; Munari, C.; Ruelle, A.; Raiteri, M. (1999). „Pharmacological diversity between native human 5-HT1B and 5-HT1D receptors sited on different neurons and involved in different functions”. British Journal of Pharmacology. 10188970 (3): 607—612. PMC 1565844 . PMID 10188970. doi:10.1038/sj.bjp.0702336.
- Goadsby, P. J.; Classey, J. D. (2003). „Evidence for serotonin (5-HT)1B, 5-HT1D and 5-HT1F receptor inhibitory effects on trigeminal neurons with craniovascular input”. Neuroscience. 14614913 (2): 491—498. PMID 14614913. S2CID 24825348. doi:10.1016/s0306-4522(03)00570-0.
semanticscholar.org
api.semanticscholar.org
- Price, G. W.; Burton, M. J.; Collin, L. J.; Duckworth, M.; Gaster, L.; Göthert, M.; Jones, B. J.; Roberts, C.; Watson, J. M.; Middlemiss, D. N. (1997). „SB-216641 and BRL-15572--compounds to pharmacologically discriminate h5-HT1B and h5-HT1D receptors”. Naunyn-Schmiedeberg's Archives of Pharmacology. 9303567 (3): 312—320. PMID 9303567. S2CID 26760453. doi:10.1007/pl00005056.
- Schlicker, E.; Fink, K.; Molderings, G. J.; Price, G. W.; Duckworth, M.; Gaster, L.; Middlemiss, D. N.; Zentner, J.; Likungu, J.; Göthert, M. (1997). „Effects of selective h5-HT1B (SB-216641) and h5-HT1D (BRL-15572) receptor ligands on guinea-pig and human 5-HT auto- and heteroreceptors”. Naunyn-Schmiedeberg's Archives of Pharmacology. 9303568 (3): 321—327. PMID 9303568. S2CID 12246022. doi:10.1007/pl00005057.
- Goadsby, P. J.; Classey, J. D. (2003). „Evidence for serotonin (5-HT)1B, 5-HT1D and 5-HT1F receptor inhibitory effects on trigeminal neurons with craniovascular input”. Neuroscience. 14614913 (2): 491—498. PMID 14614913. S2CID 24825348. doi:10.1016/s0306-4522(03)00570-0.