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1 rs was determined by measurement of original Aroclors.
2 Three represent relatively unweathered Aroclors.
3 easured in the sediment were not detected in Aroclors.
4 East Chicago, IN and five original Monsanto Aroclors.
5 sent in above-trace quantities in commercial Aroclors.
6 ater than trace concentrations in commercial Aroclors.
7 duced deletions in vivo in the mouse embryo; Aroclor 1221 and Aroclor 1260 induced deletions in yeast
9 es strongly resembled the OH-PCB profiles of Aroclors 1221, 1242, 1248, and 1254, yet 25% of OH-PCBs
10 PLA2 that are linked to different functions: Aroclor 1242 activates a calcium-independent PLA2 that r
13 AA release and O2- production in response to Aroclor 1242 were inhibited by bromoenol lactone (BEL),
14 hat are activated by the neutrophil stimuli, Aroclor 1242, a mixture of polychlorinated biphenyls, an
20 d placental anti-angiogenesis in response to Aroclor 1254 (A-1254), a mixture of polychlorinated biph
21 or 6 mg/kg/day of a commercial PCB mixture, Aroclor 1254 (A1254) by gavage from gestational day (GD)
26 e effects of ecologically relevant levels of Aroclor 1254, a polychlorinated biphenyl (PCB) mixture,
27 tive stress were influenced mainly by PB and Aroclor 1254, indicative of an oxidative damage response
28 rs (beta-naphthoflavone, phenobarbital (PB), Aroclor 1254, isoniazid, pregnenolone 16alpha-carbonitri
29 ent of PCB congeners in factors, relative to Aroclor 1254, suggested biotransformation (via cytochrom
32 ow), 0.70 (intermediate), or 1.05 (high) mug Aroclor 1254/g-body weight by gavage from 1 through 18 d
33 nated most hexa- and heptachlorobiphenyls in Aroclor 1260 (50 mug/mL) leading to losses of 51% and 20
34 high molecular weight formulations, such as Aroclor 1260 and PCBs 206, 208, and 209 produced during
38 responsible for extensive dechlorination of Aroclor 1260, and finally to the identification of a Deh
39 D14 dechlorinated the commercial PCB mixture-Aroclor 1260-mainly by removing flanked para- and doubly
42 B-209, which was manufactured at the site in Aroclor 1270 and 1271, was the most abundant congener in
44 to report levels of OH-PCBs in sediment and Aroclors, and our discovery is significant because it is
45 highly weathered as to be unrecognizable as Aroclors, and thus have probably resided in the river fo
46 factors were probably originally related to Aroclors, but they are so highly weathered as to be unre
49 L laboratory mesocosms containing weathered Aroclor-contaminated sediment from Baltimore Harbor, MD,
50 ilized Aroclors (gaseous PCBs) and unaltered Aroclors (dissolved PCBs) dominate in some samples, ongo
52 between schools and indicated the sources as Aroclors from building materials and individual PCBs ass
53 rization indicated that although volatilized Aroclors (gaseous PCBs) and unaltered Aroclors (dissolve
54 se commercial mixtures of PCBs, analogous to Aroclors in the United States) is reduced from 20- or 50
55 f non-Aroclor PCB congeners (</=0.20 wt % in Aroclor) in human serum collected from urban and rural a
58 olescents have significantly lower total non-Aroclor PCB concentrations than mothers in East Chicago
61 There are significant differences in non-Aroclor PCBs between East Chicago community and Columbus
64 PCBs) dominate in some samples, ongoing non-Aroclor sources such as paints/pigments (PCB 11) and coa
65 exhibited congener patterns consistent with Aroclor weathering, suggesting potential PCB metabolism
67 with high potency (EC50=1.4 microM), whereas Aroclors with either high or low chlorine composition sh
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