Tumor suppressor p53 cooperates with SIRT6 to regulate gluconeogenesis by promoting FoxO1 nuclear exclusion
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Title
Tumor suppressor p53 cooperates with SIRT6 to regulate gluconeogenesis by promoting FoxO1 nuclear exclusion
Authors
Keywords
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Journal
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
Volume 111, Issue 29, Pages 10684-10689
Publisher
Proceedings of the National Academy of Sciences
Online
2014-07-10
DOI
10.1073/pnas.1411026111
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- SIRT6 Promotes DNA Repair Under Stress by Activating PARP1
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- Applications of post-translational modifications of FoxO family proteins in biological functions
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- Cytosolic FoxO1 is essential for the induction of autophagy and tumour suppressor activity
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- Human SIRT6 Promotes DNA End Resection Through CtIP Deacetylation
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- Blinded by the Light: The Growing Complexity of p53
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- Arginine Methylation of FOXO Transcription Factors Inhibits Their Phosphorylation by Akt
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- A fasting inducible switch modulates gluconeogenesis via activator/coactivator exchange
- (2008) Yi Liu et al. NATURE
- p53 regulates glucose metabolism through an IKK-NF-κB pathway and inhibits cell transformation
- (2008) Keiko Kawauchi et al. NATURE CELL BIOLOGY
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