Histaminski H3 receptor (Serbian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Histaminski H3 receptor" in Serbian language version.

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16nih.gov

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9doi.org

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5web.archive.org

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5aspetjournals.org

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2archive.org

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1ebi.ac.uk

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archive.org

Bakker, RA (2004). „Histamine H₃-receptor isoforms”. Inflamm. Res. 53 (10): 509—16. PMID 15597144. doi:10.1007/s00011-004-1286-9.
Schlicker E, Betz R, Göthert M (1988). „Histamine H₃ receptor-mediated inhibition of serotonin release in the rat brain cortex”. Naunyn Schmiedebergs Arch. Pharmacol. 337 (5): 588—90. PMID 3412497. doi:10.1007/BF00182737.

aspetjournals.org

jpet.aspetjournals.org

Tedford CE, Phillips JG, Gregory R, Pawlowski GP, Fadnis L, Khan MA, Ali SM, Handley MK, Yates SL (1999). „Development of trans-2-(1H-imidazol-4-yl) cyclopropane derivatives as new high-affinity histamine H₃ receptor ligands”. J. Pharmacol. Exp. Ther. 289 (2): 1160—8. PMID 10215700. Архивирано из оригинала (abstract) 07. 01. 2009. г. Приступљено 16. 07. 2012.
Hatta E, Yasuda K, Levi R (1997). „Activation of histamine H₃ receptors inhibits carrier-mediated norepinephrine release in a human model of protracted myocardial ischemia”. J. Pharmacol. Exp. Ther. 283 (2): 494—500. PMID 9353362. Архивирано из оригинала (abstract) 30. 06. 2008. г. Приступљено 16. 07. 2012.
Levi R, Smith NC (2000). „Histamine H₃-receptors: a new frontier in myocardial ischemia”. J. Pharmacol. Exp. Ther. 292 (3): 825—30. PMID 10688593. Архивирано из оригинала (abstract) 02. 12. 2008. г. Приступљено 16. 07. 2012.

molpharm.aspetjournals.org

West RE, Zweig A, Shih NY, Siegel MI, Egan RW, Clark MA (1990). „Identification of two H₃-histamine receptor subtypes”. Mol. Pharmacol. 38 (5): 610—3. PMID 2172771. Архивирано из оригинала (abstract) 21. 11. 2008. г. Приступљено 15. 07. 2012.
Lovenberg TW, Roland BL, Wilson SJ, Jiang X, Pyati J, Huvar A, Jackson MR, Erlander MG (1999). „Cloning and functional expression of the human histamine H₃ receptor”. Mol. Pharmacol. 55 (6): 1101—7. PMID 10347254. Архивирано из оригинала (abstract) 06. 09. 2008. г. Приступљено 16. 07. 2012.

doi.org

Attoub S, Moizo L, Sobhani I, Laigneau JP, Lewin MJ, Bado A (2001). „The H₃ receptor is involved in cholecystokinin inhibition of food intake in rats”. Life Sci. 69 (4): 469—78. PMID 11459437. doi:10.1016/S0024-3205(01)01138-9.
Bakker, RA (2004). „Histamine H₃-receptor isoforms”. Inflamm. Res. 53 (10): 509—16. PMID 15597144. doi:10.1007/s00011-004-1286-9.
Rouleau A, Héron A, Cochois V, Pillot C, Schwartz JC, Arrang JM (2004). „Cloning and expression of the mouse histamine H₃ receptor: evidence for multiple isoforms”. J. Neurochem. 90 (6): 1331—8. PMID 15341517. doi:10.1111/j.1471-4159.2004.02606.x.
Passani MB, Lin JS, Hancock A, Crochet S, Blandina P (2004). „The histamine H₃ receptor as a novel therapeutic target for cognitive and sleep disorders”. Trends Pharmacol. Sci. 25 (12): 618—25. PMID 15530639. doi:10.1016/j.tips.2004.10.003.
Medhurst SJ, Collins SD, Billinton A, Bingham S, Dalziel RG, Brass A, Roberts JC, Medhurst AD, Chessell IP (2008). „Novel histamine H3 receptor antagonists GSK189254 and GSK334429 are efficacious in surgically-induced and virally-induced rat models of neuropathic pain.”. Pain. 138 (1): 61—78. PMID 18164820. doi:10.1016/j.pain.2007.11.006.
Leurs R, Bakker RA, Timmerman H, de Esch IJ (2005). „The histamine H₃ receptor: from gene cloning to H3 receptor drugs”. Nature reviews. Drug discovery. 4 (2): 107—20. PMID 15665857. doi:10.1038/nrd1631.
Arrang JM, Garbarg M, Schwartz JC (1983). „Auto-inhibition of brain histamine release mediated by a novel class (H₃) of histamine receptor”. Nature. 302 (5911): 832—7. PMID 6188956. doi:10.1038/302832a0.
Schlicker E, Betz R, Göthert M (1988). „Histamine H₃ receptor-mediated inhibition of serotonin release in the rat brain cortex”. Naunyn Schmiedebergs Arch. Pharmacol. 337 (5): 588—90. PMID 3412497. doi:10.1007/BF00182737.
Toyota H, Dugovic C, Koehl M, Laposky AD, Weber C, Ngo K, Wu Y, Lee DH, Yanai K, Sakurai E, Watanabe T, Liu C, Chen J, Barbier AJ, Turek FW, Fung-Leung WP, Lovenberg TW (2002). „Behavioral characterization of mice lacking histamine H₃ receptors”. Mol. Pharmacol. 62 (2): 389—97. PMID 12130692. doi:10.1124/mol.62.2.389.

ebi.ac.uk

„InterPro: IPR003980 Histamine H3 receptor”. InterPro. European Bioinformatics Institute.

nih.gov

ncbi.nlm.nih.gov

West RE, Zweig A, Shih NY, Siegel MI, Egan RW, Clark MA (1990). „Identification of two H₃-histamine receptor subtypes”. Mol. Pharmacol. 38 (5): 610—3. PMID 2172771. Архивирано из оригинала (abstract) 21. 11. 2008. г. Приступљено 15. 07. 2012.
Attoub S, Moizo L, Sobhani I, Laigneau JP, Lewin MJ, Bado A (2001). „The H₃ receptor is involved in cholecystokinin inhibition of food intake in rats”. Life Sci. 69 (4): 469—78. PMID 11459437. doi:10.1016/S0024-3205(01)01138-9.
Bakker, RA (2004). „Histamine H₃-receptor isoforms”. Inflamm. Res. 53 (10): 509—16. PMID 15597144. doi:10.1007/s00011-004-1286-9.
Rouleau A, Héron A, Cochois V, Pillot C, Schwartz JC, Arrang JM (2004). „Cloning and expression of the mouse histamine H₃ receptor: evidence for multiple isoforms”. J. Neurochem. 90 (6): 1331—8. PMID 15341517. doi:10.1111/j.1471-4159.2004.02606.x.
Tedford CE, Phillips JG, Gregory R, Pawlowski GP, Fadnis L, Khan MA, Ali SM, Handley MK, Yates SL (1999). „Development of trans-2-(1H-imidazol-4-yl) cyclopropane derivatives as new high-affinity histamine H₃ receptor ligands”. J. Pharmacol. Exp. Ther. 289 (2): 1160—8. PMID 10215700. Архивирано из оригинала (abstract) 07. 01. 2009. г. Приступљено 16. 07. 2012.
Passani MB, Lin JS, Hancock A, Crochet S, Blandina P (2004). „The histamine H₃ receptor as a novel therapeutic target for cognitive and sleep disorders”. Trends Pharmacol. Sci. 25 (12): 618—25. PMID 15530639. doi:10.1016/j.tips.2004.10.003.
Medhurst SJ, Collins SD, Billinton A, Bingham S, Dalziel RG, Brass A, Roberts JC, Medhurst AD, Chessell IP (2008). „Novel histamine H3 receptor antagonists GSK189254 and GSK334429 are efficacious in surgically-induced and virally-induced rat models of neuropathic pain.”. Pain. 138 (1): 61—78. PMID 18164820. doi:10.1016/j.pain.2007.11.006.
Leurs R, Bakker RA, Timmerman H, de Esch IJ (2005). „The histamine H₃ receptor: from gene cloning to H3 receptor drugs”. Nature reviews. Drug discovery. 4 (2): 107—20. PMID 15665857. doi:10.1038/nrd1631.
Arrang JM, Garbarg M, Schwartz JC (1983). „Auto-inhibition of brain histamine release mediated by a novel class (H₃) of histamine receptor”. Nature. 302 (5911): 832—7. PMID 6188956. doi:10.1038/302832a0.
Schlicker E, Betz R, Göthert M (1988). „Histamine H₃ receptor-mediated inhibition of serotonin release in the rat brain cortex”. Naunyn Schmiedebergs Arch. Pharmacol. 337 (5): 588—90. PMID 3412497. doi:10.1007/BF00182737.
Hatta E, Yasuda K, Levi R (1997). „Activation of histamine H₃ receptors inhibits carrier-mediated norepinephrine release in a human model of protracted myocardial ischemia”. J. Pharmacol. Exp. Ther. 283 (2): 494—500. PMID 9353362. Архивирано из оригинала (abstract) 30. 06. 2008. г. Приступљено 16. 07. 2012.
Lovenberg TW, Roland BL, Wilson SJ, Jiang X, Pyati J, Huvar A, Jackson MR, Erlander MG (1999). „Cloning and functional expression of the human histamine H₃ receptor”. Mol. Pharmacol. 55 (6): 1101—7. PMID 10347254. Архивирано из оригинала (abstract) 06. 09. 2008. г. Приступљено 16. 07. 2012.
Levi R, Smith NC (2000). „Histamine H₃-receptors: a new frontier in myocardial ischemia”. J. Pharmacol. Exp. Ther. 292 (3): 825—30. PMID 10688593. Архивирано из оригинала (abstract) 02. 12. 2008. г. Приступљено 16. 07. 2012.
Toyota H, Dugovic C, Koehl M, Laposky AD, Weber C, Ngo K, Wu Y, Lee DH, Yanai K, Sakurai E, Watanabe T, Liu C, Chen J, Barbier AJ, Turek FW, Fung-Leung WP, Lovenberg TW (2002). „Behavioral characterization of mice lacking histamine H₃ receptors”. Mol. Pharmacol. 62 (2): 389—97. PMID 12130692. doi:10.1124/mol.62.2.389.

pubmed.ncbi.nlm.nih.gov

Krueger KM, Witte DG, Ireland-Denny L, Miller TR, Baranowski JL, Buckner S, Milicic I, Esbenshade TA, Hancock AA. G protein-dependent pharmacology of histamine H3 receptor ligands: evidence for heterogeneous active state receptor conformations. Journal of Pharmacology and Experimental Therapeutics. 2005 Jul;314(1):271-81. PMID 15821027
Esbenshade TA, Fox GB, Krueger KM, Baranowski JL, Miller TR, Kang CH, Denny LI, Witte DG, Yao BB, Pan JB, Faghih R, Bennani YL, Williams M, Hancock AA. Pharmacological and behavioral properties of A-349821, a selective and potent human histamine H3 receptor antagonist. Biochemical Pharmacology. 2004 September 1;68(5):933-45. PMID 15294456

web.archive.org

West RE, Zweig A, Shih NY, Siegel MI, Egan RW, Clark MA (1990). „Identification of two H₃-histamine receptor subtypes”. Mol. Pharmacol. 38 (5): 610—3. PMID 2172771. Архивирано из оригинала (abstract) 21. 11. 2008. г. Приступљено 15. 07. 2012.
Tedford CE, Phillips JG, Gregory R, Pawlowski GP, Fadnis L, Khan MA, Ali SM, Handley MK, Yates SL (1999). „Development of trans-2-(1H-imidazol-4-yl) cyclopropane derivatives as new high-affinity histamine H₃ receptor ligands”. J. Pharmacol. Exp. Ther. 289 (2): 1160—8. PMID 10215700. Архивирано из оригинала (abstract) 07. 01. 2009. г. Приступљено 16. 07. 2012.
Hatta E, Yasuda K, Levi R (1997). „Activation of histamine H₃ receptors inhibits carrier-mediated norepinephrine release in a human model of protracted myocardial ischemia”. J. Pharmacol. Exp. Ther. 283 (2): 494—500. PMID 9353362. Архивирано из оригинала (abstract) 30. 06. 2008. г. Приступљено 16. 07. 2012.
Lovenberg TW, Roland BL, Wilson SJ, Jiang X, Pyati J, Huvar A, Jackson MR, Erlander MG (1999). „Cloning and functional expression of the human histamine H₃ receptor”. Mol. Pharmacol. 55 (6): 1101—7. PMID 10347254. Архивирано из оригинала (abstract) 06. 09. 2008. г. Приступљено 16. 07. 2012.
Levi R, Smith NC (2000). „Histamine H₃-receptors: a new frontier in myocardial ischemia”. J. Pharmacol. Exp. Ther. 292 (3): 825—30. PMID 10688593. Архивирано из оригинала (abstract) 02. 12. 2008. г. Приступљено 16. 07. 2012.