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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.
8 ominent roles in xenobiotic detoxication and procarcinogen activation.
9                  CYP1A1 bioactivates several procarcinogens and detoxifies several xenobiotic compoun
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
12                         The bioactivation of procarcinogens by cytochrome P450 2W1 may be of signific
13                          Thus, activation of procarcinogens by P450 lB1 may contribute to human tumor
14  the enzyme in tumors, in that activation of procarcinogens could lead to the accumulation of mutatio
15                                    Using the procarcinogen diethylnitrosamine (DEN) to initiate tumor
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
20 ) are important enzymes that detoxicate many procarcinogens, including HAAs.
21 A2 can catalyze the bioactivation of several procarcinogens, indicating a potential role in chemical
22                            In all nodules of procarcinogen-induced murine hepatocellular carcinomas (
23 P450 2W1 catalyzed the activation of several procarcinogens, particularly polycyclic hydrocarbon diol
24        Metabolism of food- and tobacco-borne procarcinogens results in the exposure of DNA to toxic a
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
30 mbers, which have the capacity to metabolize procarcinogens to genotoxic carcinogens.
31 he cytochrome P450 enzymes, which metabolize procarcinogens to their activated forms.
32 key to block the conversion of environmental procarcinogens to their carcinogenic metabolites in both
33                          Two major groups of procarcinogens, tobacco-specific nitrosamines and polycy
34                                        These procarcinogens undergo metabolic activation by N-oxidati

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