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Open AccessJournal ArticleDOI

Aryl Hydrocarbon Receptor (AhR) Ligands as Selective AhR Modulators: Genomic Studies.

TLDR
Like ligands for other receptors, AhR ligands are selective AhR modulators (SAhRMs) which exhibit variable tissue-, organ- and species-specific genomic and functional activities.
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This article is published in Current Opinion in Toxicology.The article was published on 2018-10-01 and is currently open access. It has received 43 citations till now. The article focuses on the topics: Aryl hydrocarbon receptor.

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Citations
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Characterization of a murine Ahr null allele: Involvement of the Ah receptor in hepatic growth and development (dioxiny2,3,7,8-tetrachlorodibenzo-p-dioxinygene targetingyliver)

TL;DR: The Ah receptor (AHR) is a ligand-activated transcription factor that mediates a pleiotropic response to environmental contaminants such as benzo(a)pyrene and 2,3,7,8-tetrachlorodibenzo-p-dioxin this paper.
Journal ArticleDOI

AHR in the intestinal microenvironment: safeguarding barrier function.

TL;DR: In this article, Stockinger, Shah, and Wincent discuss AHR regulation, its role in various intestinal cell types and in intestinal inflammation and tumorigenesis, outlining the currently known physiological functions in immune, epithelial, endothelial and neuronal cells of the intestine.
Journal ArticleDOI

Aryl Hydrocarbon Receptor (AHR) Ligands as Selective AHR Modulators (SAhRMs).

TL;DR: Data is provided suggesting that ligands for the AhR are selective AhR modulators (SAhRMs) that exhibit tissue/cell-specific AhR agonist and antagonist activities, and that their functional diversity is similar to selective receptor modulators that target steroid hormone and other nuclear receptors.

Aryl hydrocarbon receptor (AHR)-regulated transcriptomic changes in rats sensitive or resistant to major dioxin toxicities

TL;DR: The major toxic effects of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) appear to result from dysregulation of mRNA levels mediated by the aryl hydrocarbon receptor (AHR).
Journal ArticleDOI

Kynurenine emerges from the shadows - Current knowledge on its fate and function.

TL;DR: A review of the current knowledge of kynurenine fate and function can be found in this article, where the authors emphasize its importance for vital physiological and pathological processes, including inflammation and carcinogenesis.
References
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Journal ArticleDOI

2,3,7,8-Tetrachlorodibenzo-p-Dioxin and Related Halogenated Aromatic Hydrocarbons: Examination of the Mechanism of Toxicity

TL;DR: The toxicity of halogenated aromatic hydrocarbons appears to be due to the sustained expression of a normal cellular regulatory system, of which the author was previously unaware.
Journal ArticleDOI

Polychlorinated biphenyls (PCBs), dibenzo-p-dioxins (PCDDs), dibenzofurans (PCDFs), and related compounds: environmental and mechanistic considerations which support the development of toxic equivalency factors (TEFs).

TL;DR: The most toxic halogenated aromatic is 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) and based on in vivo and in vitro studies the relative toxicities have been determined relative to TCDD (i.e., toxic equivalents).

Polychlorinated biphenyls (PCBs), dibenzo-p-dioxins (PCDDs), dibenzofurans (PCDFs) and related compounds : environmental and mechanistic considerations with support the development of toxic equivalency factors (TEFs)

S. Safe
TL;DR: The most toxic halogenated aromatic is 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) as discussed by the authors.
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