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Volumn 4, Issue 5, 2012, Pages 587-588

Nuclear receptors as pharmaceutical targets: Rise of FXR and rebirth of PPAR?

Author keywords

cdk5; fibrates; FXR; glitazars; metabolic disorders; PPAR; thiazolidindiones

Indexed keywords

2,4 THIAZOLIDINEDIONE DERIVATIVE; CELL NUCLEUS RECEPTOR; FARNESOID X RECEPTOR; FIBRIC ACID DERIVATIVE; PEROXISOME PROLIFERATOR ACTIVATED RECEPTOR; PEROXISOME PROLIFERATOR ACTIVATED RECEPTOR ALPHA; PEROXISOME PROLIFERATOR ACTIVATED RECEPTOR GAMMA; PIOGLITAZONE; ROSIGLITAZONE; TESAGLITAZAR; TROGLITAZONE;

EID: 84859466432     PISSN: 17568919     EISSN: 17568927     Source Type: Journal    
DOI: 10.4155/fmc.12.8     Document Type: Editorial
Times cited : (10)

References (8)
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    • Tesaglitazar, a dual PPAR-a/g agonist. Hamster carcinogenicity, investigative animal and clinical studies
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    • Improvement of physiochemical properties of the tetrahydroazepinoindole series of farnesoid X receptor (FXR) agonists: beneficial modulation of lipids in primates
    • Lundquist J.T, Harnish DC, Kim CY et al. Improvement of physiochemical properties of the tetrahydroazepinoindole series of farnesoid X receptor (FXR) agonists: beneficial modulation of lipids in primates. J. Med. Chem. 53, 1774-1787 (2010).
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.