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1 toxicant and common environmental pollutant trichloroethylene.
2 metabolite of the environmental contaminant, trichloroethylene.
3 ins that constituted 12% of the reacted [14C]trichloroethylene.
4 covalently modified during the oxidation of trichloroethylene.
5 t also the chlorinated aliphatic hydrocarbon trichloroethylene.
6 degrading environmental pollutants, such as trichloroethylene, 2,4,5-trichlorophenoxyacetic acid (2,
7 ted ethenes (CEs) such as perchloroethylene, trichloroethylene and dichloroethylene are notorious gro
8 erformance with regards to the metabolism of trichloroethylene and the removal of a range of other to
9 redict concentration profiles of acetone and trichloroethylene and their intermediates and byproducts
10 lerant to the solvent effects of toluene and trichloroethylene at levels exceeding those of many radi
12 tive dehalogenation of perchloroethylene and trichloroethylene by vitamin B(12) produces approximatel
15 ay all derive from the unstable intermediate trichloroethylene epoxide that was trapped by reaction w
16 s to have a high maximum intensity score for trichloroethylene exposure (OR 3.3, 95% CI 1.0-10.3).
17 studies were conducted to determine whether trichloroethylene exposure is neurotoxic to the nigrostr
18 studies showing that oral administration of trichloroethylene for 6 weeks instigated selective compl
22 rom Burkholderia cepacia G4 is implicated in trichloroethylene oxidation and is uniquely suggested to
23 xidation products, accounting for 84% of the trichloroethylene oxidized, were carbon monoxide, formic
24 inhalation and dermal exposure from handling trichloroethylene-soaked metal parts had Parkinson's dis
25 ee workers with workstations adjacent to the trichloroethylene source and subjected to chronic inhala
27 erse birth outcomes among mothers exposed to trichloroethylene (TCE) and tetrachloroethylene [or perc
28 ecting aqueous tetrachloroethylene (PCE) and trichloroethylene (TCE) as low as 80 and 74 microg/L in
30 eport the electrocatalytic dehalogenation of trichloroethylene (TCE) by single soft nanoparticles in
31 ies of oxidation of dichloroethene (DCE) and trichloroethylene (TCE) by three mutant strains of Pseud
32 agnetic field (AC EMF) to effectively remove trichloroethylene (TCE) from groundwater and saturated s
33 of aged (iron oxide coated) Fe(0) to degrade trichloroethylene (TCE) has revealed that, while neither
34 GC) adapted for the in situ determination of trichloroethylene (TCE) in indoor air in support of vapo
35 C mixtures composed of acetone, ethanol, and trichloroethylene (TCE) in pentane and methanol and acet
37 cy (EPA) completed a toxicological review of trichloroethylene (TCE) in September 2011, which was the
38 echlorination of perchloroethylene (PCE) and trichloroethylene (TCE) is a potential strategy for clea
45 e applied to the automated classification of trichloroethylene (TCE) signatures from passive Fourier
46 ontinuous, short-term measurements of indoor trichloroethylene (TCE) vapor concentrations related to
49 o detect parts-per-billion concentrations of trichloroethylene (TCE) with a detection sensitivity of
50 tion Agency has identified quantification of trichloroethylene (TCE), an industrial solvent, in breas
51 odel for the destruction of (1) acetone, (2) trichloroethylene (TCE), and (3) polyethylene glycol (PE
53 thesis of this study was that metabolites of trichloroethylene (TCE), dichloroethylene (DCE) and rela
57 ts toluene, 1,1,1-trichloroethane (TCE), and trichloroethylene (TCY) affect ligand-gated ion channel
59 sing four common environmental contaminants (trichloroethylene, tetrachloroethylene, methyl tert-buty
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