Cross-talk between peroxisome proliferator-activated receptor (PPAR) α and liver X receptor (LXR) in nutritional regulation of fatty acid metabolism. I. PPARS suppress sterol regulatory element binding protein-1c promoter through inhibition of LXR signaling

Molecular Endocrinology

Volumn 17, Issue 7, 2003, Pages 1240-1254

  Yoshikawa, Tomohiro ^a   Ide, Tomohiro ^b   Shimano, Hitoshi ^b   Yahagi, Naoya ^b   Amemiya Kudo, Michiyo ^a   Matsuzaka, Takashi ^b   Yatoh, Shigeru ^b   Kitamine, Tetsuya ^a   Okazaki, Hiroaki ^a   Tamura, Yoshiaki ^a   Sekiya, Motohiro ^a   Takahashi, Akimitsu ^b   Hasty, Alyssa H ^a   Sato, Ryuichiro ^a   Sone, Hirohito ^b   Osuga, Jun Ichi ^a   Ishibashi, Shun ^a   Yamada, Nobuhiro ^b  

^a UNIVERSITY OF TOKYO   (Japan)

^b UNIVERSITY OF TSUKUBA   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

CELL NUCLEUS RECEPTOR; LIGAND; LIVER X RECEPTOR; LUCIFERASE; PEROXISOME PROLIFERATOR ACTIVATED RECEPTOR AGONIST; PEROXISOME PROLIFERATOR ACTIVATED RECEPTOR ALPHA; RECEPTOR; RETINOID X RECEPTOR; STEROL REGULATORY ELEMENT BINDING PROTEIN; STEROL REGULATORY ELEMENT BINDING PROTEIN 1C; TRANSCRIPTION FACTOR; UNCLASSIFIED DRUG;

ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; DNA RESPONSIVE ELEMENT; DOSE RESPONSE; FATTY ACID METABOLISM; FATTY ACID OXIDATION; GENE DELETION; GENE EXPRESSION; GENE MUTATION; IMMUNOPRECIPITATION; MOUSE; NONHUMAN; NORTHERN BLOTTING; NUTRITION; PRIORITY JOURNAL; RECEPTOR BINDING; REGULATOR GENE;

ANIMALS; ANTICHOLESTEREMIC AGENTS; CCAAT-ENHANCER-BINDING PROTEINS; CELLS, CULTURED; DNA-BINDING PROTEINS; FATTY ACIDS; GENE EXPRESSION REGULATION; HEPATOCYTES; HUMANS; LIVER; MALE; MICE; MICE, INBRED C57BL; NUTRITION PHYSIOLOGY; PROMOTER REGIONS (GENETICS); PYRIMIDINES; RATS; RATS, SPRAGUE-DAWLEY; RECEPTORS, CYTOPLASMIC AND NUCLEAR; RECEPTORS, RETINOIC ACID; RESPONSE ELEMENTS; RETINOID X RECEPTORS; SIGNAL TRANSDUCTION; STEROL REGULATORY ELEMENT BINDING PROTEIN 1; SULFONAMIDES; TRANSCRIPTION FACTORS;

ANIMALIA;

EID: 12444256363     PISSN: 08888809     EISSN: None     Source Type: Journal    
DOI: 10.1210/me.2002-0190     Document Type: Article

References (64)

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