Leukotriene als Mediatoren in der Pathogenese des Schocks
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Publisher
Springer Berlin Heidelberg
Link
http://link.springer.com/content/pdf/10.1007/978-3-642-84317-4_137.pdf
Reference16 articles.
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2. Denzlinger C, Guhlmann A, Scheuber PH, Wilker D, Hammer DK, Keppler D (1986) Metabolism and analysis of cysteinyl leukotrienes in the monkey. J Biol Chem 261:15601–15606.
3. Drazen JM, Austen KF, Lewis RA, Clark DA, Goto G, Marfat A, Corey EJ (1980) Comparative airway and vascular activities of leukotrienes-Cl and D in vivo and in vitro. Proc Natl Acad Sci USA 77:4354–4358.
4. Gillard J, Ford-Hutchinson AW, Chan C, et al. (1989) L-663,536 (MK-886) (3-[1-(4-chlorobenzyl)-3-t-butyl-thio-5-isopropylindol-2-yl]-2,2-dimethylpropanoic acid), a novel, orally active leukotriene biosynthesis inhibitor. Can J Physiol Pharmacol 67:456–464.
5. Guhlmann A, Keppler A, Kästner S, Krieter H, Brückner ÜB, Messmer K, Keppler D (1989) Prevention of endogenous leukotriene production during anaphylaxis in the guinea pig by an inhibitor of leukotriene biosynthesis (MK-886) but not by dexamethasone. J Exp Med 170:1905–1918.
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