↑ Wood, William F; Watson, Richard L; Largent, David L (October 1998). "Phenol, the odour compound from Agaricus praeclaresquamosus". Biochemical Systematics and Ecology. 26 (7): 793–794. Bibcode:1998BioSE..26..793W. doi:10.1016/S0305-1978(98)00058-1.
1 2 3 Chilton, WS; Ott, J (1976). "Toxic metabolites of Amanita pantherina, A. cothurnata, A. muscaria, and other Amanita species". Lloydia. 39 (2–3): 150–7. ISSN0024-5461. PMID985999.
↑ Andreas., Bresinsky (1990). A colour atlas of poisonous fungi: a handbook for pharmacists, doctors, and biologists. Besl, Helmut. London, England: Wolfe Pub. ISBN978-0723415763. OCLC22547396.[pageneeded]
↑ De Bernardi, Maria; Mellerio, Giorgio; Vidari, Giovanni; Vita-Finzi, Paola; Fronza, Giovanni; Kocòr, Marian; St. Pyrek, Jan (May 1981). "Fungal Metabolites. IX. Triterpenes From Naematoloma sublateritium". Journal of Natural Products. 44 (3): 351–356. Bibcode:1981JNAtP..44..351D. doi:10.1021/np50015a020. ISSN0163-3864.
1 2 Lurie, Yael; Wasser, Solomon P.; Taha, Muhammad; Shehade, Haj; Nijim, Josef; Hoffmann, Yoav; Basis, Fuad; Vardi, Moshe; Lavon, Ophir (2009-07-01). "Mushroom poisoning from species of genus Inocybe (fiber head mushroom): a case series with exact species identification". Clinical Toxicology. 47 (6): 562–565. doi:10.1080/15563650903008448. ISSN1556-3650. PMID19566380. S2CID205902282.
↑ Clark, Ernest D.; Smith, Clayton S. (1913). "Toxicological Studies on the Mushrooms Clitocybe Illudens and Inocybe Infida". Mycologia. 5 (4): 224–232. doi:10.2307/3753387. JSTOR3753387.
↑ Tanaka, K.; Inoue, T.; Kadota, S.; Kikuchi, T. (1990-01-01). "Metabolism of illudin S, a toxic principle of Lampteromyces japonicus, by rat liver. I. Isolation and identification of cyclopropane ring-cleavage metabolites". Xenobiotica. 20 (7): 671–681. doi:10.3109/00498259009046883. ISSN0049-8254. PMID2238702.
↑ Tanaka, K.; Inoue, T.; Kadota, S.; Kikuchi, T. (1992-01-01). "Metabolism by rat liver cytosol of illudin S, a toxic substance of Lampteromyces japonicus. II. Characterization of illudin S-metabolizing enzyme". Xenobiotica. 22 (1): 33–39. doi:10.3109/00498259209053100. ISSN0049-8254. PMID1377439.
↑ Tanaka, K.; Inoue, T.; Tezuka, Y.; Kikuchi, T. (1996-01-01). "Metabolism of illudin S, a toxic substance of Lampteromyces japonicus: urinary excretion of mercapturic acids in rat". Xenobiotica. 26 (3): 347–354. doi:10.3109/00498259609046713. ISSN0049-8254. PMID8730925.
↑ Burgess, Maree L.; Barrow, Kevin D. (1999-01-01). "Biosynthesis of illudosin, a fomannosane-type sesquiterpene, by the Basidiomycete Omphalotus nidiformis". Journal of the Chemical Society, Perkin Transactions 1 (17): 2461–2466. doi:10.1039/A904097H. ISSN1364-5463.
↑ Puschner, Birgit (2007). "Mushroom toxins". Veterinary Toxicology. pp.915–925. doi:10.1016/B978-012370467-2/50169-3. ISBN978-0-12-370467-2. Omphalotus olearius, Omphalotus subilludens, and Lampteromyces japonicus contain illudin S (Bresinsky and Besl, 1990b). Illudin S is a sesquiterpene with a unique chemical structure. In humans, vomiting and diarrhea occur 1–2.5 h after ingestion (French and Garrettson, 1988).
↑ R., Benjamin, Denis (1995). Mushrooms: poisons and panaceas: a handbook for naturalists, mycologists, and physicians. New York: W.H. Freeman. ISBN978-0716726005. OCLC31708814.{{cite book}}: CS1 maint: multiple names: authors list (link)[pageneeded]
↑ Hallen, Heather E; Watling, Roy; Adams, Gerard C (2003-08-01). "Taxonomy and toxicity of Conocybe lactea and related species". Mycological Research. 107 (8): 969–979. doi:10.1017/S0953756203008190. ISSN0953-7562. PMID14531619.
↑ Licastro, F; Morini, MC; Kretz, O; Dirheimer, G; Creppy, EE; Stirpe, F (1 May 1993). "Mitogenic activity and immunological properties of bolesatine, a lectin isolated from the mushroom Boletus satanas Lenz". The International Journal of Biochemistry. 25 (5): 789–92. doi:10.1016/0020-711X(93)90366-M. ISSN0020-711X. PMID8349019.
↑ Pinto, Andrea; Conti, Paola; Amici, Marco De; Tamborini, Lucia; Madsen, Ulf; Nielsen, Birgitte; Christesen, Thomas; Bräuner-Osborne, Hans; Micheli, Carlo De (2008-04-01). "Synthesis and Pharmacological Characterization at Glutamate Receptors of the Four Enantiopure Isomers of Tricholomic Acid". Journal of Medicinal Chemistry. 51 (7): 2311–2315. doi:10.1021/jm701394a. ISSN0022-2623. PMID18338843.
This page is based on this Wikipedia article Text is available under the CC BY-SA 4.0 license; additional terms may apply. Images, videos and audio are available under their respective licenses.