Shin-ichiro Imai
Affiliations: | Biology & Biomedical Sciences (Molecular Cell Biology) | Washington University, Saint Louis, St. Louis, MO |
Area:
Neuroscience Biology, Cell Biology, AgingGoogle:
"Shin-ichiro Imai"Children
Sign in to add trainee| Kathryn A. Moynihan | grad student | 2006 | Washington University |
| Javier R. Revollo | grad student | 2006 | Washington University |
| Myeong J. Yoon | grad student | 2012 | Washington University |
| Liana L. Stein | grad student | 2014 | Washington University |
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Publications
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| Yoshida M, Satoh A, Lin JB, et al. (2019) Extracellular Vesicle-Contained eNAMPT Delays Aging and Extends Lifespan in Mice. Cell Metabolism |
| Snyder-Warwick AK, Satoh A, Santosa KB, et al. (2018) Hypothalamic Sirt1 protects terminal Schwann cells and neuromuscular junctions from age-related morphological changes. Aging Cell. e12776 |
| Johnson S, Imai SI. (2018) NAD biosynthesis, aging, and disease. F1000research. 7: 132 |
| Satoh A, Imai SI, Guarente L. (2017) The brain, sirtuins, and ageing. Nature Reviews. Neuroscience. 18: 362-374 |
| Mills KF, Yoshida S, Stein LR, et al. (2016) Long-Term Administration of Nicotinamide Mononucleotide Mitigates Age-Associated Physiological Decline in Mice. Cell Metabolism. 24: 795-806 |
| Stromsdorfer KL, Yamaguchi S, Yoon MJ, et al. (2016) NAMPT-Mediated NAD(+) Biosynthesis in Adipocytes Regulates Adipose Tissue Function and Multi-organ Insulin Sensitivity in Mice. Cell Reports |
| de Picciotto NE, Gano LB, Johnson LC, et al. (2016) Nicotinamide mononucleotide supplementation reverses vascular dysfunction and oxidative stress with aging in mice. Aging Cell |
| Stein LR, Zorumski CF, Imai SI, et al. (2015) Nampt is required for long-term depression and the function of GluN2B subunit-containing NMDA receptors. Brain Research Bulletin |
| Yoon MJ, Yoshida M, Johnson S, et al. (2015) SIRT1-Mediated eNAMPT Secretion from Adipose Tissue Regulates Hypothalamic NAD+ and Function in Mice. Cell Metabolism. 21: 706-17 |
| Ghisays F, Brace CS, Yackly SM, et al. (2015) The N-Terminal Domain of SIRT1 Is a Positive Regulator of Endogenous SIRT1-Dependent Deacetylation and Transcriptional Outputs. Cell Reports |