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8


Article dans une revue7 documents

  • Laura A. Mertens, Hamza Labiad, Otoniel Denis-Alpizar, Martin Fournier, David Carty, et al.. Rotational energy transfer in collisions between CO and Ar at temperatures from 293 to 30 K. Chemical Physics Letters, Elsevier, 2017, 683, pp.521-528. 〈10.1016/j.cplett.2017.05.052〉. 〈hal-01578397〉
  • Yannick Boireaud, Tatiana Carlson, Martin Fournier, Xavier Le Berre Castillo, Dinesh Outtandy, et al.. Parle-t-on mal d’économie dans les médias ? Les résultats d’une enquête nationale. Idées économiques et sociales, Réseau Canopé, 2015, 2 (180), pp. 6-23. 〈10.3917/idee.180.0006〉. 〈halshs-01234555〉
  • Jessica F. Lockyear, Martin Fournier, Ian R. Sims, Jean-Claude Guillemin, Craig A. Taatjes, et al.. Formation of fulvene in the reaction of C2H with 1,3-butadiene. International Journal of Mass Spectrometry, Elsevier, 2015, 378, pp.232-245. 〈10.1016/j.ijms.2014.08.025〉. 〈hal-01069616〉
  • M Gust, M Fortier, J Garric, Martin Fournier, F Gagné. Immunotoxicity of surface waters contaminated by municipal effluents to the snail Lymnaea stagnalis.. Aquatic Toxicology, Elsevier, 2013, 126, pp.393-403. 〈10.1016/j.aquatox.2012.09.001〉. 〈pasteur-01131050〉
  • F Gagné, J Auclair, M Fortier, A Bruneau, Martin Fournier, et al.. Bioavailability and immunotoxicity of silver nanoparticles to the freshwater mussel Elliptio complanata.. Journal of Toxicology and Environmental Health, Part A: Current Issues, Taylor & Francis, 2013, 76 (13), pp.767-77. 〈10.1080/15287394.2013.818602〉. 〈pasteur-01130978〉
  • M Gust, M Fortier, J Garric, Martin Fournier, F Gagné. Effects of short-term exposure to environmentally relevant concentrations of different pharmaceutical mixtures on the immune response of the pond snail Lymnaea stagnalis.. The Science of the total environment., 2013, 445-446, pp.210-8. 〈10.1016/j.scitotenv.2012.12.057〉. 〈pasteur-01131048〉
  • Jordy Bouwman, Martin Fournier, Ian R Sims, Stephen Leone, Kevin Wilson. Reaction Rate and Isomer-Specific Product Branching Ratios of C2H + C4H8: 1-Butene, cis-2-Butene, trans-2-Butene, and Isobutene at 79 K.. Journal of Physical Chemistry A, American Chemical Society, 2013, 117 (24), pp.5093-5105. 〈10.1021/jp403637t〉. 〈hal-00844546〉

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