Nuclear receptor subfamily 1, group H, member 2
Nuclear hormone receptor-like domain superfamily
Nuclear hormone receptor, ligand-binding domain
nuclear hormone receptor-type zinc finger
DNA-binding transcription factor activity
positive regulation of high-density lipoprotein particle assembly
positive regulation of triglyceride biosynthetic process
Nuclear hormone receptor, ligand-binding domain, protein family
Zinc finger, nuclear hormone receptor-type, protein family
DNA-binding transcription activator activity, RNA polymerase II-specific
RNA polymerase II transcription regulator complex
positive regulation of protein metabolic process
positive regulation of cholesterol transport
Regulation of the aldo-keto reductase gene akr1b7 by the nuclear oxysterol receptor LXRalpha (liver X receptor-alpha) in the mouse intestine: putative role of LXRs in lipid detoxification processes
Isolation of proteins that interact specifically with the retinoid X receptor: two novel orphan receptors
ABCA12 regulates ABCA1-dependent cholesterol efflux from macrophages and the development of atherosclerosis
SIRT1 deacetylates and positively regulates the nuclear receptor LXR
Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium
Pancreatic exocrine insufficiency in LXRbeta-/- mice is associated with a reduction in aquaporin-1 expression
Ligand activation of LXR beta reverses atherosclerosis and cellular cholesterol overload in mice lacking LXR alpha and apoE
Liver X receptor (LXR)-beta regulation in LXRalpha-deficient mice: implications for therapeutic targeting
Non-redundant roles for LXRalpha and LXRbeta in atherosclerosis susceptibility in low density lipoprotein receptor knockout mice
Liver X receptor activation controls intracellular cholesterol trafficking and esterification in human macrophages
Identification of oxysterol 7alpha-hydroxylase (Cyp7b1) as a novel retinoid-related orphan receptor alpha (RORalpha) (NR1F1) target gene and a functional cross-talk between RORalpha and liver X receptor (NR1H3)
Both liver-X receptor (LXR) isoforms control energy expenditure by regulating brown adipose tissue activity