A comprehensive review of Sirtuins: With a major focus on redox homeostasis and metabolism
出版年份 2021 全文链接
标题
A comprehensive review of Sirtuins: With a major focus on redox homeostasis and metabolism
作者
关键词
Sirtuins, Metabolism, Oxidative stress, Antioxidant defense, Post-translational modification, Transcriptional regulation
出版物
LIFE SCIENCES
Volume 282, Issue -, Pages 119803
出版商
Elsevier BV
发表日期
2021-07-06
DOI
10.1016/j.lfs.2021.119803
参考文献
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- Sirt3-Mediated Deacetylation of Evolutionarily Conserved Lysine 122 Regulates MnSOD Activity in Response to Stress
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- Sirtuin 1 Modulates Cellular Responses to Hypoxia by Deacetylating Hypoxia-Inducible Factor 1α
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- Adiponectin and AdipoR1 regulate PGC-1α and mitochondria by Ca2+ and AMPK/SIRT1
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- SIRT1 is regulated by a PPARγ–SIRT1 negative feedback loop associated with senescence
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- Sirtuin 3, a New Target of PGC-1α, Plays an Important Role in the Suppression of ROS and Mitochondrial Biogenesis
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- Hepatocyte-Specific Deletion of SIRT1 Alters Fatty Acid Metabolism and Results in Hepatic Steatosis and Inflammation
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- SIRT1 Promotes Cell Survival under Stress by Deacetylation-Dependent Deactivation of Poly(ADP-Ribose) Polymerase 1
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- AMPK regulates energy expenditure by modulating NAD+ metabolism and SIRT1 activity
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- JNK1 Phosphorylates SIRT1 and Promotes Its Enzymatic Activity
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- SIRT1 Regulates Apoptosis and Nanog Expression in Mouse Embryonic Stem Cells by Controlling p53 Subcellular Localization
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- Sirt7 Increases Stress Resistance of Cardiomyocytes and Prevents Apoptosis and Inflammatory Cardiomyopathy in Mice
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- SIRT1 Modulation of the Acetylation Status, Cytosolic Localization, and Activity of LKB1
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- SIRT1 Regulates Hepatocyte Lipid Metabolism through Activating AMP-activated Protein Kinase
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- Substrates and Regulation Mechanisms for the Human Mitochondrial Sirtuins Sirt3 and Sirt5
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- Necdin Regulates p53 Acetylation via Sirtuin1 to Modulate DNA Damage Response in Cortical Neurons
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- SIRT2 Suppresses Adipocyte Differentiation by Deacetylating FOXO1 and Enhancing FOXO1's Repressive Interaction with PPARγ
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- A fasting inducible switch modulates gluconeogenesis via activator/coactivator exchange
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- DBC1 is a negative regulator of SIRT1
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- miR-34a repression of SIRT1 regulates apoptosis
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