Accès gratuit
Numéro
Med Sci (Paris)
Volume 24, Numéro 11, Novembre 2008
Page(s) 947 - 953
Section M/S revues
DOI https://doi.org/10.1051/medsci/20082411947
Publié en ligne 15 novembre 2008
  1. Shaw AJ, Goffinet B. Bryophyte bology. Cambridge : Cambridge University Press, 2000 : 476 p.
  2. De Sloover JL. Hépatiques, mousses et muscinées. Namur : Presses Universitaires, 1997 : 194 p.
  3. Glime JM, Saxena D. Uses of Bryophytes. New Delhi : Today and Tomorrow’s Printers and Publishers, 1991 : 100 p.
  4. Glime JM. Medicines and antibiotics. In : Bryophyte ecology, vol. 5, 2007. http://www.bryoecol.mtu.edu/.
  5. Asakawa Y. Chemical constituents of the bryophytes. Wien-New York : Springer Verlag, 1995 : 618 p.
  6. Asakawa Y. Biologically active compounds from bryophytes. Pure Appl Chem 2007; 79 : 557–80.
  7. Ainge GD, Gerard PJ, Hinkley SF, et al. Hodgsonox, a new class of sesquiterpene from the liverwort Lepidolaena hodgsoniae. Isolation directed by insecticidal activity. J Org Chem 2001; 66 : 2818–21.
  8. McCleary JA, Sypherd PS, Walkington DL. Mosses as possible sources of antibiotics. Science 1960; 131 : 108.
  9. Kahn A. Des plantes et des hommes. Med Sci (Paris) 2001; 17 : 825–8.
  10. Scher JM, Speakman JB, Zapp J, et al. Bioactivity guided isolation of antifungal compounds from the liverwort Bazzania trilobata (L.) S.F. Gray. Phytochemistry 2004; 65 : 2583–8.
  11. Spjut RW, Suffness M, Cragg GM, et al. Mosses, liverworts, and hornworts screened for antitumor agents. Econ Bot 1986; 40 : 310–38.
  12. Arnal I, Sassoon I, Tournebize R. Dynamique du fuseau : vers une cible anti-cancéreuse. Med Sci (Paris) 2002; 18 : 1227–35.
  13. Pommier Y, Kohn KW. Cycle cellulaire et points de contrôle : nouvelles cibles thérapeutiques. Med Sci (Paris) 2003; 19 : 173–86.
  14. Sakai K, Ichikawa T, Yamada K, et al. Antitumor principles in mosses : the first isolation and identification of maytansinoids, including a novel 15-methoxyansamitocin P-3. J Nat Prod 1988; 51 : 845–50.
  15. Suwanborirux K, Chang CJ, Spjut RW, et al. Ansamitocin P-3, a maytansinoid, from Claopodium crispifolium and Anomodon attenuatus or associated actinomycetes. Experientia 1990; 46 : 117–20.
  16. Perry NB, Burgess EJ, Tangney RS. Cytotoxic 8,9-secokaurane diterpenes from a New Zealand liverwort, Lepidolaena taylorii. Tetrahedron Lett 1996; 37 : 9387–90.
  17. Perry NB, Burgess EJ, Baek SH, et al. 11-oxygenated cytotoxic 8,9-secokauranes from a New Zealand liverwort, Lepidolaena taylorii. Phytochemistry 1999; 50 : 423–33.
  18. Perry NB, Burgess EJ, Baek SH, et al. The first atisane diterpenoids from a liverwort : polyols from Lepidolaena clavigera. Org Lett 2001; 3 : 4243–5.
  19. Nagashima F, Kasai W, Kondoh M, et al. New ent-kaurene-type diterpenoids possessing cytotoxicity from the New Zealand liverwort Jungermannia species. Chem Pharm Bull (Tokyo) 2003; 51 : 1189–92.
  20. Nagashima F, Kondoh M, Fujii M, et al. Novel cytotoxic kaurane-type diterpenoids from the New Zealand Liverwort Jungermannia species. Tetrahedron 2005; 61 : 4531–44.
  21. Kondoh M, Nagashima F, Suzuki I, et al. Induction of apoptosis by new ent-kaurene-type diterpenoids isolated from the New Zealand liverwort Jungermannia species. Planta Med 2005; 71 : 1005–9.
  22. Wu C, Gunatilaka AA, McCabe FL, et al. Bioactive and other sesquiterpenes from Chiloscyphus rivularis. J Nat Prod 1997; 60 : 1281–6.
  23. Scher JM, Burgess EJ, Lorimer SD, et al. A cytotoxic sesquiterpene and unprecedented sesquiterpene-bisbibenzyl compounds from the liverwort Schistochila glaucescens. Tetrahedron 2002; 58 : 7875–82.
  24. Spjut RW, Cassady JM, McCloud T, et al. Variation in cytotoxicity and antitumor activity among samples of the moss Claopodium crispifolium (Thuidiaceae). Econ Bot 1988; 42 : 62–72.
  25. Davey ML, Currah RS. Interactions between mosses (Bryophyta) and fungi. Can J Bot 2006; 84 : 1509–19.
  26. Opelt K, Berg G. Diversity and antagonistic potential of bacteria associated with bryophytes from nutrient-poor habitats of the Baltic sea coast. Appl Environ Microbiol 2004; 70 : 6569–79.
  27. Read DJ, Ducket JG, Francis R, et al. Symbiotic fungal associations in « lower » land plants. Philos Trans R Soc Lond B Biol Sci 2000; 355 : 815–31.
  28. Cassady JM, Chan KK, Floss HG, et al. Recent developments in the maytansinoid antitumor agents. Chem Pharm Bull (Tokyo) 2004; 52 : 1–26.
  29. Siddiqui IR, Singh PK, Singh J. Synthesis and fungicidal activity of novel 4,4’-bis(2’ ‘-aryl-5’ -methyl/unsubstituted-4’ ‘-oxo-thiazolidin-3’ ‘-yl) bibenzyl. J Agric Food Chem 2003; 51 : 7062–5.
  30. Barrero AF, Herrador MM, Quilez del Moral JF, et al. Couplings of benzylic halides mediated by titanocene chloride : synthesis of bibenzyl derivatives. J Org Chem 2007; 72 : 2251–4.
  31. Hohe A, Reski R. From axenic spore germination to molecular farming. One century of bryophyte in vitro culture. Plant Cell Rep 2005; 23 : 513–21.
  32. Kingston DG. Taxol and its analogs. In : Cragg GM, Kingston DG, Newman DJ, eds. Anticancer agents from natural products. Boca Raton : CRC Press, 2005 : 89–122.

Les statistiques affichées correspondent au cumul d'une part des vues des résumés de l'article et d'autre part des vues et téléchargements de l'article plein-texte (PDF, Full-HTML, ePub... selon les formats disponibles) sur la platefome Vision4Press.

Les statistiques sont disponibles avec un délai de 48 à 96 heures et sont mises à jour quotidiennement en semaine.

Le chargement des statistiques peut être long.