核受体
受体
过氧化物酶体增殖物激活受体
过氧化物酶体
过氧化物酶体增殖物激活受体α
功能(生物学)
过氧化物酶体增殖物激活受体γ
基因
生物
计算生物学
细胞生物学
药理学
化学
生物化学
生物信息学
转录因子
作者
Barry G. Shearer,William J. Hoekstra
标识
DOI:10.2174/0929867033368295
摘要
The peroxisome proliferator-activated receptor (PPAR) family of nuclear receptors, a set of three receptor sub-types encoded by distinct genes, function as lipid sensors to regulate a broad range of genes in many metabolically active tissues. Synthetic PPAR agonists have exhibited therapeutic benefits in treating diabetes and cardiovascular diseases. The discovery of PPAR-specific ligands has led to significant advancement in our understanding of the structure of these receptor proteins and the molecular mechanism of their ligand-dependent activation. Herein, we present both recent progress in the functional analysis of these orphan receptors and the confirmation of the PPARs as molecular targets for the development of new medicines to treat human metabolic disease.
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