Articles dans des revues avec comité de lecture (40)
  1. 17. Laport, M. S., Bauwens, M., de Oliveira Nunes, S., Willenz, P., George, I., & Muricy, G. R. D. S. (2017). Culturable bacterial communities associated to Brazilian Oscarella species (Porifera: Homoscleromorpha) and their antagonistic interactions. Antonie van Leeuwenhoek, 110(4), 489-499. doi:10.1007/s10482-016-0818-y
  2. 18. Bouhajja, E., McGuire, M. K. M., Liles, M. R., Bataille, G., AGATHOS, S., & George, I. (2017). Identification of novel toluene monooxygenase genes in a hydrocarbon-polluted sediment using sequence- and function-based screening of metagenomic libraries. Applied microbiology and biotechnology, 101(2), 797-808. doi:10.1007/s00253-016-7934-5
  3. 19. Bouhajja, E., AGATHOS, S., & George, I. (2016). Metagenomics: Probing pollutant fate in natural and engineered ecosystems. Biotechnology advances, 34(8), 1413-1426. doi:10.1016/j.biotechadv.2016.10.006
  4. 20. Laport, M. S., Pontes, P. V. M., dos Santos, D. S., Santos-Gandelman, J. D. F., Muricy, G. R. D. S., Bauwens, M., Giambiagi-deMarval, M., & George, I. (2016). Antibiotic resistance genes detected in the marine sponge Petromica citrina from Brazilian coast. Brazilian journal of microbiology, 47(3), 617-620. doi:10.1016/j.bjm.2016.04.016
  5. 21. Bouhajja, E., Efthymiopoulos, T., George, I., Moreels, D., Van Houdt, R., Mergeay, M., & AGATHOS, S. (2016). Conjugative transfer of broad host range plasmids to an acidobacterial strain, Edaphobacter aggregans. Journal of biotechnology, 221, 107-113. doi:10.1016/j.jbiotec.2016.01.025
  6. 22. Laport, M. S., Santos-Gandelman, J. D. F., Muricy, G. R. D. S., Giambiagi-deMarval, M., & George, I. (2016). Antagonistic interactions among bacteria isolated from either the same or from different sponges native to the Brazilian coast. Journal of Marine Science and Application, 6(2).
  7. 23. Van Aarle, I., Perimenis, A., Lima-Ramos, J., De Hults, E., George, I., & Gerin, P. A. (2015). Mixed inoculum origin and lignocellulosic substrate type both influence the production of volatile fatty acids during acidogenic fermentation. Biochemical engineering journal, 103, 242-249. doi:10.1016/j.bej.2015.07.016
  8. 24. Ye, L., Santos-Gandelman, J. D. F., Hardoim, C. C. P., George, I., Cornelis, P., & Laport, M. S. (2015). Antibacterial activity and mutagenesis of sponge-associated Pseudomonas fluorescens H41. Antonie van Leeuwenhoek, 108(1), 117-126. doi:10.1007/s10482-015-0469-4
  9. 25. Da Rocha, U. N., Plugge, C. C., George, I., Van Elsas, J. D., & Van Overbeek, L. S. (2013). The rhizosphere selects for particular groups of Acidobacteria and Verrucomicrobia. PloS one, 9(4), e94514. doi:10.1371/journal.pone.0094514
  10. 26. George, I., Hartmann, M., Liles, M. R., & Agathos, S. (2011). Recovery of as-yet uncultured soil Acidobacteria on dilute solid media. Applied and environmental microbiology, 77, 8184-8188.
  11. 27. Parsley, L. C., Linneman, J., Goode, A. M., Becklund, K., George, I., Goodman, R. M., Lopanik, N. B., & Liles, M. R. (2011). Polyketide synthase pathways identified from an arrayed metagenomic library are derived from soil Acidobacteria. FEMS microbiology, ecology, 78(1), 176-187.
  12. 28. Liles, M. R., Turkmen, O., Manske, B. F., Zhang, M., Rouillard, J.-M., George, I., Balser, T., Billor, N., & Goodman, R. M. (2010). A phylogenetic microarray targeting 16S rRNA genes from the bacterial division Acidobacteria reveals a lineage-specific distribution in a soil clay fraction. Soil biology & biochemistry, 42, 739-747.
    13. << Précédent 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 Suivant >>