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1 ching of bSULT1A1 fluorescence observed with pentachlorophenol.
2 nd hexachlorobenzene were oxidized slowly to pentachlorophenol.
3 ganism capable of complete mineralization of pentachlorophenol.
4 induced in S. chlorophenolica in response to pentachlorophenol.
5 , 2,4-dichlorophenol, 2,4,5-trichlorophenol, pentachlorophenol, 4-nitrobenzyl-chloride, 2,4-dichloroa
11 ,6-dichlorohydroquinone in the catabolism of pentachlorophenol by Sphingobium chlorophenolicum ATCC 3
18 contaminated soil from the United States and pentachlorophenol from a certified reference material (C
20 reactions in the pathway for degradation of pentachlorophenol in the soil bacterium Sphingobium chlo
21 , 2,4-dichlorophenol, 2,4,6-trichlorophenol, pentachlorophenol) in river water was accomplished using
22 atalysts, to destroy the priority pollutants pentachlorophenol (PCP) and 2,4,6-trichlorophenol (TCP).
23 transferase and acetyltransferase inhibitors pentachlorophenol (PCP) and 2,6-dichloro-4-nitrophenol (
24 perfund wood-treating site contaminated with pentachlorophenol (PCP) and the environmentally persiste
32 from soil that was heavily contaminated with pentachlorophenol (PCP), a toxic pesticide introduced in
33 ites of polychlorinated biphenyls (OH-PCBs), pentachlorophenol (PCP), and perfluorooctane sulfonate (
34 produced not by the most-highly chlorinated pentachlorophenol (PCP), but rather by the less chlorina
35 nd their hydroxylated metabolites (HO-PCBs), pentachlorophenol (PCP), polybrominated diphenyl ethers,
36 c sludge, with or without 10 mg L(-1) spiked pentachlorophenol (PCP), we found it was clear that the
38 nsforming phenolic organic compounds such as pentachlorophenol, phenolic acids, and triclosan via sur
39 enoxide at pH 8.3, midway between the pKa of pentachlorophenol (pKa = 4.8) and that of hydrogen perox
40 n, forchlorfenuron, imidacloprid, malathion, pentachlorophenol, pyraclostrobin, sulfasalazine, and tr
41 tyi strain JNA in pure culture dechlorinated pentachlorophenol to 3,5-dichlorophenol (DCP) via remova
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