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1 reserved tissues of rodents treated with the procarcinogens.
2 , is essential for the bioactivation of many procarcinogens.
3 ltered metabolic activation of tobacco smoke procarcinogens.
4 of androgenic steroids and certain aromatic procarcinogens.
5 A13 (CYP2A13) activates the nicotine-derived procarcinogen 4-(methylnitrosamino)-1-(3-pyridyl)-1-buta
6 nt in tobacco, and activation of the tobacco procarcinogen 4-(methylnitrosamino)-1-(3-pyridyl)-1-buta
7 0s participate in xenobiotic detoxification, procarcinogen activation, and steroid hormone synthesis.
10 tivation of hexamethylphosphoramide, a nasal procarcinogen, and 2,6-dichlorobenzonitrile (DCBN), a he
11 ign of chemopreventive strategies is whether procarcinogen bioactivation in an extrahepatic target ti
14 the enzyme in tumors, in that activation of procarcinogens could lead to the accumulation of mutatio
16 been shown to be formed in DNA from various procarcinogens (e.g., acrolein, malonaldehyde, vinyl chl
17 none, is one of the most potent and abundant procarcinogens found in tobacco and tobacco smoke, and g
18 ic aromatic hydrocarbons (PAHs), is a potent procarcinogen generated during the combustion of fossil
19 the dispositions of reactive metabolites of procarcinogens in humans, provided that exposures are ad
21 A2 can catalyze the bioactivation of several procarcinogens, indicating a potential role in chemical
23 P450 2W1 catalyzed the activation of several procarcinogens, particularly polycyclic hydrocarbon diol
25 mportant enzymes in the detoxication of many procarcinogens, serve as a mechanism of bioactivation of
26 of benzo[a]pyrene (B[a]P), an environmental procarcinogen that activates Cyp1a1 transcriptional resp
27 yclic amines (HCAs) found in cooked meat are procarcinogens that are metabolically activated by N-hyd
28 els should be applicable to studies on other procarcinogens that require P450-mediated metabolic acti
29 ertain hepatotoxic chemicals, including some procarcinogens, their ability to monooxygenate, and ther
32 key to block the conversion of environmental procarcinogens to their carcinogenic metabolites in both
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