Flavone antagonists bind competitively with 2,3,7, 8-tetrachlorodibenzo-p-dioxin (TCDD) to the aryl hydrocarbon receptor but inhibit nuclear uptake and transformation
about
An aryl hydrocarbon receptor conformation acts as the functional core of nuclear dioxin signaling.Development of novel CH223191-based antagonists of the aryl hydrocarbon receptorDietary polyphenols increase paraoxonase 1 gene expression by an aryl hydrocarbon receptor-dependent mechanism.A ligand for the aryl hydrocarbon receptor isolated from lung.Mechanism-based common reactivity pattern (COREPA) modelling of aryl hydrocarbon receptor binding affinity.Suppression of cytokine-mediated complement factor gene expression through selective activation of the Ah receptor with 3',4'-dimethoxy-α-naphthoflavoneAryl hydrocarbon receptor-dependent retention of nuclear HuR suppresses cigarette smoke-induced cyclooxygenase-2 expression independent of DNA-binding.Cord blood expansion. Pyrimidoindole derivatives are agonists of human hematopoietic stem cell self-renewalAryl hydrocarbon receptor ligands in cancer: friend and foe.Lightening up the UV response by identification of the arylhydrocarbon receptor as a cytoplasmatic target for ultraviolet B radiation.Agonist and chemopreventative ligands induce differential transcriptional cofactor recruitment by aryl hydrocarbon receptor.Novel 2-amino-isoflavones exhibit aryl hydrocarbon receptor agonist or antagonist activity in a species/cell-specific context.Activation of the aryl hydrocarbon receptor by TCDD inhibits senescence: a tumor promoting event?Functional expression of aryl hydrocarbon receptor on mast cells populating human endometriotic tissues.(-)-Epigallocatechin-3-gallate is a novel Hsp90 inhibitorMolecular determinants of species-specific agonist and antagonist activity of a substituted flavone towards the aryl hydrocarbon receptor.Structural identification of Diindole agonists of the aryl hydrocarbon receptor derived from degradation of indole-3-pyruvic acidAryl Hydrocarbon Receptor Diet and Breast Cancer Risk.
P2860
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P2860
Flavone antagonists bind competitively with 2,3,7, 8-tetrachlorodibenzo-p-dioxin (TCDD) to the aryl hydrocarbon receptor but inhibit nuclear uptake and transformation
description
1999 nî lūn-bûn
@nan
1999 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
Flavone antagonists bind compe ...... lear uptake and transformation
@ast
Flavone antagonists bind compe ...... lear uptake and transformation
@en
Flavone antagonists bind compe ...... lear uptake and transformation
@nl
type
label
Flavone antagonists bind compe ...... lear uptake and transformation
@ast
Flavone antagonists bind compe ...... lear uptake and transformation
@en
Flavone antagonists bind compe ...... lear uptake and transformation
@nl
prefLabel
Flavone antagonists bind compe ...... lear uptake and transformation
@ast
Flavone antagonists bind compe ...... lear uptake and transformation
@en
Flavone antagonists bind compe ...... lear uptake and transformation
@nl
P2093
P3181
P1476
Flavone antagonists bind compe ...... lear uptake and transformation
@en
P2093
J J Willey
M J Totleben
R S Pollenz
S D Dertinger
T A Gasiewicz
P304
P3181
P407
P577
1999-04-01T00:00:00Z