One important xenobiotic consumed daily by millions of people worldwide is alcohol.
2
Furthermore, the topical application of CBA significantly increased the levels of xenobiotic enzymes.
3
This epidemic may be affected by exposure to xenobiotic chemicals.
4
The contribution of cytosolic enzymes to xenobiotic metabolism may be remarkable in extrahepatic tissues.
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Exposure to xenobiotic compounds is global concern influencing the world population as a health hazard.
Ús de xenobiotics en anglès
1
These findings show that mammalian kidney is highly active in bioactivation of xenobiotics.
2
Filter-feeding organisms accumulate xenobiotics and other substances in their tissues.
3
Primary hepatocytes are a model for studying various effects of different xenobiotics, including detoxification strategies.
4
Prediction of response to environmental stimuli, xenobiotics and diet.
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Additionally, it has long been appreciated that exposure to drug metabolism-inducing xenobiotics can impair immune function.
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Recent studies have demonstrated that endogenous chemicals are also oxidized by human P450s which mainly metabolize xenobiotics.
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There is a wide promiscuity of these receptors in the induction of CYPs in response to xenobiotics.
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Adverse effects of xenobiotics reported earlier might be camouflaged by beneficial eel constituents, such as n-3 fatty acids.
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The cytochrome P450 enzymes are highly expressed in the liver and are involved in the metabolism of xenobiotics.
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The molecular functions of these genes have been associated with the metabolism of lipids and detoxification of xenobiotics.
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Our understanding of ocular toxicities from xenobiotics in humans, livestock, and wildlife is growing thanks to laboratory animal models.
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Polymorphism of MDR1 gene is connected with reduction of P-glycoprotein expression in placenta and increased fetal exposure to xenobiotics.
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It is unknown whether AEA can influence fetal concentrations of xenobiotics by modulating the expression of transporters in syncytiotrophoblasts.
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This result is supported by studies that show glutathione conjugation of some xenobiotics by the GSTs can produce mutagenic intermediates.
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Such a multi-analytical approach will potentially provide an information-rich platform for the elucidation of effects of xenobiotics and drug efficacy studies.
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As a consequence of mutations in the genes coding for transmembrane protein pumps, the intracellular concentration of xenobiotics may significantly increase.