Calorie restriction-induced SIRT6 activation delays aging by suppressing NF-κB signaling
Published 2016 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Calorie restriction-induced SIRT6 activation delays aging by suppressing NF-κB signaling
Authors
Keywords
-
Journal
CELL CYCLE
Volume 15, Issue 7, Pages 1009-1018
Publisher
Informa UK Limited
Online
2016-03-04
DOI
10.1080/15384101.2016.1152427
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- The journey of resveratrol from yeast to human
- (2016) Silvie Timmers et al. Aging-US
- Interventions to Slow Aging in Humans: Are We Ready?
- (2015) Valter D. Longo et al. AGING CELL
- Global analyses revealed age-related alterations in innate immune responses after stimulation of pathogen recognition receptors
- (2015) Talibah U. Metcalf et al. AGING CELL
- Serum from calorie-restricted animals delays senescence and extends the lifespan of normal human fibroblasts in vitro
- (2015) Rafael de Cabo et al. Aging-US
- The importance of the p50 NF-κB subunit
- (2015) Neil D Perkins CELL CYCLE
- Energy excess is the main cause of accelerated aging of mammals
- (2015) Tomasz Biliński et al. Oncotarget
- SnapShot: Sirtuins, NAD, and Aging
- (2014) Takashi Nakagawa et al. Cell Metabolism
- SIRT6 Regulates Osteogenic Differentiation of Rat Bone Marrow Mesenchymal Stem Cells Partially via Suppressing the Nuclear Factor-κB Signaling Pathway
- (2014) Hualing Sun et al. STEM CELLS
- SIRT3 overexpression antagonizes high glucose accelerated cellular senescence in human diploid fibroblasts via the SIRT3–FOXO1 signaling pathway
- (2013) Bin Zhang et al. AGE
- The transformative promise of aging science
- (2012) David Stipp CELL CYCLE
- The sirtuin SIRT6 regulates lifespan in male mice
- (2012) Yariv Kanfi et al. NATURE
- Liver cancer initiation is controlled by AP-1 through SIRT6-dependent inhibition of survivin
- (2012) Lihua Min et al. NATURE CELL BIOLOGY
- The sirtuin SIRT6 blocks IGF-Akt signaling and development of cardiac hypertrophy by targeting c-Jun
- (2012) Nagalingam R Sundaresan et al. NATURE MEDICINE
- SIRT6 overexpression induces massive apoptosis in cancer cells but not in normal cells
- (2011) Michael Van Meter et al. CELL CYCLE
- Histone acetyltransferases are crucial regulators in NF-κB mediated inflammation
- (2011) Massimo Ghizzoni et al. DRUG DISCOVERY TODAY
- SIRT6 Promotes DNA Repair Under Stress by Activating PARP1
- (2011) Z. Mao et al. SCIENCE
- The Histone Deacetylase Sirt6 Regulates Glucose Homeostasis via Hif1α
- (2010) Lei Zhong et al. CELL
- Human SIRT6 Promotes DNA End Resection Through CtIP Deacetylation
- (2010) Abderrahmane Kaidi et al. SCIENCE
- Linking calorie restriction to longevity through sirtuins and autophagy: any role for TOR
- (2010) M V Blagosklonny Cell Death & Disease
- SIRT6 Links Histone H3 Lysine 9 Deacetylation to NF-κB-Dependent Gene Expression and Organismal Life Span
- (2009) Tiara L.A. Kawahara et al. CELL
- NF-κB Signaling in the Aging Process
- (2009) Antero Salminen et al. JOURNAL OF CLINICAL IMMUNOLOGY
- Beneficial effect of Bupleurum polysaccharides on autoimmune disease induced by Campylobacter jejuni in BALB/c mice
- (2009) Zheng Wang et al. JOURNAL OF ETHNOPHARMACOLOGY
- Caloric Restriction Delays Disease Onset and Mortality in Rhesus Monkeys
- (2009) R. J. Colman et al. SCIENCE
- Glucose Restriction Inhibits Skeletal Myoblast Differentiation by Activating SIRT1 through AMPK-Mediated Regulation of Nampt
- (2008) Marcella Fulco et al. DEVELOPMENTAL CELL
- SIRT6 is a histone H3 lysine 9 deacetylase that modulates telomeric chromatin
- (2008) Eriko Michishita et al. NATURE
- Activation of innate immunity system during aging: NF-kB signaling is the molecular culprit of inflamm-aging
- (2007) Antero Salminen et al. AGEING RESEARCH REVIEWS
Create your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create NowAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started