000 01444 a2200397 4500
005 20250516104412.0
264 0 _c20130129
008 201301s 0 0 eng d
022 _a1520-5010
024 7 _a10.1021/tx300169e
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aMohammadi-Bardbori, Afshin
245 0 0 _aQuercetin, resveratrol, and curcumin are indirect activators of the aryl hydrocarbon receptor (AHR).
_h[electronic resource]
260 _bChemical research in toxicology
_cSep 2012
300 _a1878-84 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aCarbazoles
_xchemistry
650 0 4 _aCell Line
650 0 4 _aChromatography, High Pressure Liquid
650 0 4 _aCurcumin
_xchemistry
650 0 4 _aCytochrome P-450 CYP1A1
_xantagonists & inhibitors
650 0 4 _aHep G2 Cells
650 0 4 _aHumans
650 0 4 _aKeratinocytes
_xdrug effects
650 0 4 _aQuercetin
_xchemistry
650 0 4 _aReceptors, Aryl Hydrocarbon
_xagonists
650 0 4 _aRecombinant Proteins
_xantagonists & inhibitors
650 0 4 _aResveratrol
650 0 4 _aStilbenes
_xchemistry
700 1 _aBengtsson, Johanna
700 1 _aRannug, Ulf
700 1 _aRannug, Agneta
700 1 _aWincent, Emma
773 0 _tChemical research in toxicology
_gvol. 25
_gno. 9
_gp. 1878-84
856 4 0 _uhttps://doi.org/10.1021/tx300169e
_zAvailable from publisher's website
999 _c22002744
_d22002744