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FXR acetylation is normally dynamically regulated by p300 and SIRT1 but constitutively elevated in metabolic disease states

The nuclear bile acid receptor FXR is critical for regulation of lipid and glucose metabolism. Here we report that FXR is a target of SIRT1, a deacetylase that mediates nutritional and hormonal modulation of hepatic metabolism. Lysine 217 of FXR is the major acetylation site targeted by p300 and SIR...

詳細記述

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書誌詳細
主要な著者: Kemper, Jongsook Kim, Xiao, Zhen, Ponugoti, Bhaskar, Miao, Ji, Fang, Sungsoon, Kanamaluru, Deepthi, Tsang, Stephanie, Wu, Shwu-Yuan, Chiang, Cheng-Ming, Veenstra, Timothy D.
フォーマット: Artigo
言語:Inglês
出版事項: 2009
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC2785075/
https://ncbi.nlm.nih.gov/pubmed/19883617
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.cmet.2009.09.009
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