Title : Transgenic Overexpression of Steroid Sulfatase Alleviates Cholestasis.

Pub. Date : 2017 Jun

PMID : 29130021






5 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 Oxygenated cholesterol derivative oxysterols are known to be endogenous ligands of the liver X receptor (LXR), a nuclear receptor with anti-cholestasis activity, whereas the sulfated oxysterols antagonize LXR signaling. Oxysterols nuclear receptor subfamily 1, group H, member 3 Mus musculus
2 Oxygenated cholesterol derivative oxysterols are known to be endogenous ligands of the liver X receptor (LXR), a nuclear receptor with anti-cholestasis activity, whereas the sulfated oxysterols antagonize LXR signaling. Oxysterols nuclear receptor subfamily 1, group H, member 3 Mus musculus
3 Oxygenated cholesterol derivative oxysterols are known to be endogenous ligands of the liver X receptor (LXR), a nuclear receptor with anti-cholestasis activity, whereas the sulfated oxysterols antagonize LXR signaling. Oxysterols nuclear receptor subfamily 1, group H, member 3 Mus musculus
4 Oxygenated cholesterol derivative oxysterols are known to be endogenous ligands of the liver X receptor (LXR), a nuclear receptor with anti-cholestasis activity, whereas the sulfated oxysterols antagonize LXR signaling. Oxysterols nuclear receptor subfamily 1, group H, member 3 Mus musculus
5 The protective effect of the STS transgene was associated with the activation of LXR and induction of LXR target genes, likely because of the increased conversion of the antagonistic oxysterol sulfates to the agonistic oxysterols. Oxysterols nuclear receptor subfamily 1, group H, member 3 Mus musculus