Tham khảo Leukotriene

  1. ↑ Loick, H.; Theissen, J. (1994). “Die Eicosanoide als Mediatoren beim ARDS” [Eicosanoids as mediators in ARDS]. AINS (bằng tiếng Đức). 29 (1): 3–9. doi:10.1055/s-2007-996677. PMID 8142566.Quản lý CS1: ngôn ngữ không rõ (liên kết)
  2. ↑ Salmon, John A; Higgs, Gerald A (1987). “Prostaglandins and leukotrienes as inflammatory mediators”. British Medical Bulletin. 43 (2): 285–96. PMID 2825898.
  3. ↑ O'Byrne, Paul M.; Israel, Elliot; Drazen, Jeffrey M. (1997). “Antileukotrienes in the treatment of asthma”. Annals of Internal Medicine. 127 (6): 472–80. doi:10.7326/0003-4819-127-6-199709150-00009. PMID 9313005.
  4. ↑ Nelson, David L.; Cox, Michael M. (2008). "Leukotrienes". Lehninger Principles of Biochemistry (5th ed.). Macmillan. tr. 359. ISBN 978-0-7167-7108-1.
  5. ↑ Scott JP, Peters-Golden M (tháng 9 năm 2013). "Antileukotriene agents for the treatment of lung disease". Am. J. Respir. Crit. Care Med. 188 (5): 538–544. doi:10.1164/rccm.201301-0023PP. PMID 23822826.
  6. ↑ Feldberg, W.; Kellaway, C. H. (1938). “Liberation of histamine and formation of lysocithin-like substances by cobra venom”. The Journal of Physiology. 94 (2): 187–226. doi:10.1113/jphysiol.1938.sp003674. PMC 1393616. PMID 16995038.
  7. ↑ Feldberg, W.; Holden, H. F.; Kellaway, C. H. (1938). “The formation of lysocithin and of a muscle-stimulating substance by snake venoms”. The Journal of Physiology. 94 (2): 232–48. doi:10.1113/jphysiol.1938.sp003676. PMC 1393612. PMID 16995040.
  8. ↑ Kellaway, C. H.; Trethewie, E. R. (1940). “The Liberation of a Slow‐Reacting Smooth Muscle‐Stimulating Substance in Anaphylaxis”. Quarterly Journal of Experimental Physiology and Cognate Medical Sciences. 30 (2): 121–45. doi:10.1113/expphysiol.1940.sp000825.
  9. ↑ truy cập 24 tháng 4 năm 2012
  10. ↑ Crooks, S.W; Stockley, R.A (1998). "Leukotriene B4". The International Journal of Biochemistry & Cell Biology. 30 (2): 173–8. doi:10.1016/S1357-2725(97)00123-4. PMID 9608670.
  11. ↑ Terano, Takashi; Salmon, John A.; Moncada, Salvador (1984). "Biosynthesis and biological activity of leukotriene B5". Prostaglandins. 27 (2): 217–32. doi:10.1016/0090-6980(84)90075-3. PMID 6326200.
  12. ↑ O'Flaherty, Joseph T.; Taylor, Jennifer S.; Thomas, Michael J. (1998). “Receptors for the 5-oxo class of eicosanoids in neutrophils”. The Journal of Biological Chemistry. 273 (49): 32535–41. doi:10.1074/jbc.273.49.32535. PMID 9829988.
  13. ↑ Powell, William S.; Rokach, Joshua (2013). “The eosinophil chemoattractant 5-oxo-ETE and the OXE receptor”. Progress in Lipid Research. 52 (4): 651–65. doi:10.1016/j.plipres.2013.09.001. PMC 5710732. PMID 24056189.
  14. ↑ Manev, Radmila; Manev, Hari (2004). "5-Lipoxygenase as a Putative Link Between Cardiovascular and Psychiatric Disorders". Critical Reviews in Neurobiology. 16 (1–2): 181–6. doi:10.1615/CritRevNeurobiol.v16.i12.190. PMID 15581413.
  15. ↑ Dahlén, Sven-Erik; Björk, Jakob; Hedqvist, Per; Arfors, Karl-E.; Hammarström, Sven; Lindgren, Jan-Åke; Samuelsson, Bengt (1981). "Leukotrienes promote plasma leakage and leukocyte adhesion in postcapillary venules: in vivo effects with relevance to the acute inflammatory response". Proceedings of the National Academy of Sciences. 78 (6): 3887–91. doi:10.1073/pnas.78.6.3887. JSTOR 10943. PMC 319678. PMID 6267608.

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