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Genetic variation in the murine lifespan response to dietary restriction: from life extension to life shortening
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Summary: Chronic dietary restriction (DR) is considered among the most robust life‐extending interventions, but several reports indicate that DR does not always extend and may even shorten lifespan in some genotypes. An unbiased genetic screen of the lifespan response to DR has been lacking. Here, we measured the effect of one commonly used level of DR (40% reduction in food intake) on mean lifespan of virgin males and females in 41 recombinant inbred strains of mice. Mean strain‐specific lifespan varied two to threefold under ad libitum (AL) feeding and 6‐ to 10‐fold under DR, in males and females respectively. Notably, DR shortened lifespan in more strains than those in which it lengthened life. Food intake and female fertility varied markedly among strains under AL feeding, but neither predicted DR survival: therefore, strains in which DR shortened lifespan did not have low food intake or poor reproductive potential. Finally, strain‐specific lifespans under DR and AL feeding were not correlated, indicating that the genetic determinants of lifespan under these two conditions differ. These results demonstrate that the lifespan response to a single level of DR exhibits wide variation amenable to genetic analysis. They also show that DR can shorten lifespan in inbred mice. Although strains with shortened lifespan under 40% DR may not respond negatively under less stringent DR, the results raise the possibility that life extension by DR may not be universal.
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“Even among highly genetically similar strains of yeast or mice, dietary restriction is equally likely to shorten lifespan as to extend lifespan.76,77,78”
From Asynchronous, contagious and digital aging (2021) · cites this paper as [78]
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Citations
Cites
The Effect of Retarded Growth Upon the Length of Life Span and Upon the Ultimate Body Size
McCay, C. M., Crowell, M. F., & Maynard, L. A. (1935) · The Journal of Nutrition · doi:10.1093/jn/10.1.63 · Cited by 2,264
The retardation of aging and disease by dietary restriction
(1989) · Choice Reviews Online · doi:10.5860/choice.26-5101 · Cited by 1,477
Longevity, senescence and the genome
(1995) · General Pharmacology The Vascular System · doi:10.1016/0306-3623(95)90026-8 · Cited by 1,403
Overview of caloric restriction and ageing
Masoro, E. J. (2005) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2005.03.012 · Cited by 879
Nutrient Requirements of Laboratory Animals,
National Research Council (1995) · National Academies Press eBooks · doi:10.17226/4758 · Cited by 735
Growth Curves and Survival Characteristics of the Animals Used in the Biomarkers of Aging Program
Turturro, A., Witt, W. W., Lewis, S. M., Hass, B. S., Lipman, R. D., & Hart, R. W. (1999) · The Journals of Gerontology Series A · doi:10.1093/gerona/54.11.b492 · Cited by 675
The effect of retarded growth upon the length of life span and upon the ultimate body size. 1935.
Cm, M., Crowell, M. F., & MAYNARD, L. A. (1989) · PubMed · Cited by 670
Yu, B. P., Masoro, E. J., Murata, I., Bertrand, H. A., & Lynd, F. T. (1982) · Journal of Gerontology · doi:10.1093/geronj/37.2.130 · Cited by 580
Yuan, R., Tsaih, S., Petkova, S. B., de Evsikova, C. M., Xing, S., Marion, M. A., Bogue, M. A., Mills, K. D., Peters, L. L., Bult, C. J., et al. (2009) · Aging Cell · doi:10.1111/j.1474-9726.2009.00478.x · Cited by 422
Fontana, L., Weiss, E. P., Villareal, D. T., Klein, S., & Holloszy, J. O. (2008) · Aging Cell · doi:10.1111/j.1474-9726.2008.00417.x · Cited by 396
Cited by
Sorted by citations
Items 301–400 of 500
Caloric Restriction Alters Postprandial Responses of Essential Brain Metabolites in Young Adult Mice
Yanckello, L. M., Young, L. E. A., Hoffman, J. D., Mohney, R. P., Keaton, M., Abner, E. L., & Lin, A. (2019) · Frontiers in Nutrition · doi:10.3389/fnut.2019.00090 · Cited by 12
Comparative Medicine: An Inclusive Crossover Discipline.
Macy, J. D., & Horváth, T. L. (2017) · Europe PMC (PubMed Central) · Cited by 13
Ouellette, A. R., Hadad, N., Deighan, A. G., Robinson, L. L., O’Connell, K. M. S., Freund, A., Churchill, G. A., & Kaczorowski, C. C. (2022) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2022.07.004 · Cited by 12
Reed, A. L., Mitchell, W., Alexandrescu, A. T., & Alder, N. N. (2023) · Frontiers in Physiology · doi:10.3389/fphys.2023.1263420 · Cited by 13
Longevity. The allostatic load of dietary restriction
Pijl, H. (2011) · Physiology & Behavior · doi:10.1016/j.physbeh.2011.05.030 · Cited by 12
Kishi, S. (2013) · Translational research · doi:10.1016/j.trsl.2013.10.004 · Cited by 12
Strain- and Diet-Related Lesion Variability in Aging DBA/2, C57BL/6, and DBA/2xC57BL/6 F1 Mice
Harbison, C. E., Lipman, R. D., & Bronson, R. T. (2015) · Veterinary Pathology · doi:10.1177/0300985815612152 · Cited by 12
Functional genomics of dietary restriction and longevity in yeast
Campos, S. E., & DeLuna, A. (2019) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2019.02.003 · Cited by 13
Mulvey, L., Wilkie, S. E., Borland, G., Griffiths, K., Sinclair, A., McGuinness, D., Watson, D. G., & Selman, C. (2021) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2021.111376 · Cited by 13
Dietary Restriction: Theory Fails to Satiate
Hayflick, L. (2010) · Science · doi:10.1126/science.329.5995.1014 · Cited by 12
Alive and well? Exploring disease by studying lifespan
Brett, J. O., & Rando, T. A. (2014) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2014.05.004 · Cited by 12
Late-life shift in caloric intake affects fly metabolism and longevity
Li, M., Macro, J., Meadows, K., Mishra, D., Martin, D., Olson, S., Huggins, B., Graveley, B. R., Li, J. Y. H., & Rogina, B. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2311019120 · Cited by 12
Litichevskiy, L., Considine, M., Gill, J., Shandar, V., Cox, T. O., Descamps, H. C., Wright, K. M., Amses, K. R., Dohnalová, L., Liou, M. J., et al. (2025) · Nature Microbiology · doi:10.1038/s41564-025-01963-3 · Cited by 19
Food restriction during pregnancy alters brain’s antioxidant network in dams and their offspring
Stone, V., August, P. M., Stocher, D. P., Klein, C. P., Couto, P. R. G., Silva, Y. D., Sagini, J. P. N., Salomon, T. B., Benfato, M. S., & Matté, C. (2016) · Free Radical Research · doi:10.3109/10715762.2016.1152361 · Cited by 11
Lee, M. H., Fan, Q., Yu, L., & Zhang, Z. (2020) · Systematic and Applied Acarology · doi:10.11158/saa.25.11.2 · Cited by 11
Reversing age-associated arterial dysfunction: insight from preclinical models
Gogulamudi, V. R., Cai, J., & Lesniewski, L. A. (2018) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00086.2018 · Cited by 11
Perinatal diet influences health and survival in a mouse model of leukemia
Palliyaguru, D. L., Rudderow, A., Sossong, A. M., Lewis, K. N., Younts, C. M., Pearson, K. J., Bernier, M., & de Cabo, R. (2020) · GeroScience · doi:10.1007/s11357-020-00199-9 · Cited by 12
Impacts of Calorie Restriction and Intermittent Fasting on Health and Diseases: Current Trends
Chung, H. Y., Kim, D. H., Bang, E., & Yu, B. P. (2020) · Nutrients · doi:10.3390/nu12102948 · Cited by 11
Feeding on frozen live yeast has some deleterious effects in Drosophila melanogaster
Bourg, É. L., Gauthier, T., & Colinet, H. (2015) · Experimental Gerontology · doi:10.1016/j.exger.2015.06.019 · Cited by 11
Schleit, J., Wall, V., Simko, M., & Kaeberlein, M. R. (2011) · PLoS ONE · doi:10.1371/journal.pone.0028036 · Cited by 10
Nutritional limitation in early postnatal life and its effect on aging and longevity in rodents
Davis, K., Chamseddine, D., & Harper, J. M. (2016) · Experimental Gerontology · doi:10.1016/j.exger.2016.05.001 · Cited by 12
Ivimey‐Cook, E. R., Sultanova, Z., & Maklakov, A. A. (2025) · Aging Cell · doi:10.1111/acel.70131 · Cited by 12
Jablonsky, J., Lasher, A. T., Patki, A., Nagarajan, A., & Sun, L. Y. (2024) · Aging Cell · doi:10.1111/acel.14238 · Cited by 10
Inflammation in Aging Processes
Finch, C. E. (2010) · Elsevier eBooks · doi:10.1016/b978-0-12-378638-8.00012-9 · Cited by 10
Physiological basis for sex-specific differences in longevity
Cheng, C. J. A., & Nelson, J. F. (2018) · Current Opinion in Physiology · doi:10.1016/j.cophys.2018.04.003 · Cited by 10
Self-citationHepatic gene body hypermethylation is a shared epigenetic signature of murine longevity
Hahn, O., Stubbs, T. M., Reik, W., Grönke, S., Beyer, A., & Partridge, L. (2018) · PLoS Genetics · doi:10.1371/journal.pgen.1007766 · Cited by 10
A budding yeast's perspective on aging: The shape I'm in
Smith, J. T., Wright, J., & Schneider, B. L. (2015) · Experimental Biology and Medicine · doi:10.1177/1535370215577584 · Cited by 10
Ji, J., Sundquist, J., & Sundquist, K. (2016) · Endocrine Research · doi:10.3109/07435800.2016.1141948 · Cited by 10
Dietary restriction extends lifespan across different temperatures in the fly
Phillips, E. J., & Simons, M. J. P. (2024) · Functional Ecology · doi:10.1111/1365-2435.14563 · Cited by 9
Tao, S., Wang, Y., Yu, C., Qiu, R., Jiang, Y., Jia, J., Tao, Z., Zhang, L., Zou, B., & Tang, D. (2022) · Gut Microbes · doi:10.1080/19490976.2022.2117509 · Cited by 9
Thyne, K. M., & Salmon, A. B. (2023) · GeroScience · doi:10.1007/s11357-023-00857-8 · Cited by 9
Dobson, A. J., Voigt, S., Kumpitsch, L., Langer, L., Voigt, E., Ibrahim, R., Dowling, D. K., & Reinhardt, K. (2023) · PLoS Biology · doi:10.1371/journal.pbio.3002218 · Cited by 10
Giraldo, Y. M., Muscedere, M. L., & Traniello, J. F. A. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.673172 · Cited by 9
Future Mortality in Low Mortality Countries
Caselli, G., & Drefahl, S. (2017) · Oxford University Press eBooks · doi:10.1093/oso/9780198813422.003.0009 · Cited by 12
Emiliano, A. B., Lopatinsky, N. R., Kraljević, M., Higuchi, S., He, Y., Haeusler, R. A., & Schwartz, G. J. (2022) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00017.2022 · Cited by 9
Golightly, A., Boys, R. J., Cameron, K., & von Zglinicki, T. (2012) · Journal of the Royal Statistical Society Series C (Applied Statistics) · doi:10.1111/j.1467-9876.2012.01045.x · Cited by 9
Lee, B. P., Mulvey, L., Barr, G., Garratt, J., Goodman, E., Selman, C., & Harries, L. W. (2019) · Experimental Gerontology · doi:10.1016/j.exger.2019.110736 · Cited by 9
Frankel, S. A., & Rogina, B. (2021) · Frontiers in Genetics · doi:10.3389/fgene.2021.733184 · Cited by 8
McLean, S., Lee, M. B., Liu, W., Hameed, R., Gujjala, V. A., Zhou, X., Kaeberlein, M. R., & Kaya, A. (2024) · Frontiers in Aging · doi:10.3389/fragi.2024.1408160 · Cited by 10
Lifelong restriction of dietary valine has sex-specific benefits for health and lifespan in mice
Calubag, M. F., Ademi, I., Green, C. L., Manchanayake, D. N. H., Jayarathne, H. S. M., Marshall, R. N., Le, S. M., Lialios, P., Breuer, L. E., Yakar, S., et al. (2026) · Nature Aging · doi:10.1038/s43587-026-01169-0 · Cited by 9
Zhao, F., Zou, Z., Liu, Z., Wang, J., Wu, Y., Zhang, J., Liu, Q., Liang, W., Yao, J., Jiang, X., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-64892-z · Cited by 11
Kobyliansky, E., Torchinsky, D., Kalichman, L., & Karasik, D. (2016) · American Journal of Clinical Nutrition · doi:10.3945/ajcn.116.138040 · Cited by 8
Predicting longevity responses to dietary restriction: A stepping stone toward precision geroscience
Pérez-Matos, M. C., & Mair, W. B. (2020) · PLoS Genetics · doi:10.1371/journal.pgen.1008833 · Cited by 8
Hartwig, F. P. (2014) · Aging and Disease · doi:10.14336/ad.2014.050017 · Cited by 7
Diet effects on mouse meiotic recombination: a warning for recombination studies
Belmonte-Tebar, A., Perez, E. S. M., Nam, S., Soler, A. J., Singh, N. D., & de la Casa‐Esperón, E. (2021) · Genetics · doi:10.1093/genetics/iyab190 · Cited by 7
Liao, C., Rikke, B. A., Johnson, T. E., Diaz, V., & Nelson, J. F. (2010) · Aging Cell · doi:10.1111/j.1474-9726.2010.00564.x · Cited by 7
Self-citationMalta, A., Furlan, M. P., Vitoriano, A. D. S., Barrena, H. C., Bazotte, R. B., & Gazola, V. A. F. G. (2010) · Nutrition Research · doi:10.1016/j.nutres.2010.08.003 · Cited by 7
Hallam, D., Wan, T., & Saretzki, G. C. (2015) · Experimental Gerontology · doi:10.1016/j.exger.2015.04.014 · Cited by 8
Müller-Eigner, A., Sanz‐Moreno, A., de Diego, I., Venkatasubramani, A. V., Langhammer, M., Gerlini, R., Rathkolb, B., Aguilar‐Pimentel, J. A., Klein‐Rodewald, T., Calzada‐Wack, J., et al. (2022) · Communications Biology · doi:10.1038/s42003-022-03339-3 · Cited by 9
Shin, J. H., Pawlowski, S. W., & Warren, C. A. (2021) · Gut Microbes · doi:10.1080/19490976.2021.1966255 · Cited by 7
Short lifespan is one’s fate, long lifespan is one’s achievement: lessons from Daphnia
Beam, T. C., Bright, M. P., Pearson, A. C., Dua, I., Smith, M. L., Dutta, A. K., Bhadra, S. C., Salman, S., Strickler, C. N., Anderson, C. E., et al. (2024) · GeroScience · doi:10.1007/s11357-024-01244-7 · Cited by 6
Preserved cardiac function by vinculin enhances glucose oxidation and extends health- and life-span
Sessions, A. O., Min, P., Cordes, T., Weickert, B. J., Divakaruni, A. S., Murphy, A. N., Metallo, C. M., & Engler, A. J. (2018) · APL Bioengineering · doi:10.1063/1.5019592 · Cited by 6
Mitchell, S. J., & Mitchell, J. R. (2022) · Nutrition and Healthy Aging · doi:10.3233/nha-220162 · Cited by 9
Wide‐ranging genetic variation in sensitivity to rapamycin in Drosophila melanogaster
Harrison, B. R., Lee, M. B., Zhang, S., Young, B., Han, K., Sukomol, J., Paus, V., Tran, S., Kim, D., Fitchett, H., et al. (2024) · Aging Cell · doi:10.1111/acel.14292 · Cited by 4
Osteoporosis and Mechanisms of Skeletal Aging
Glowacki, J., & Vokes, T. (2015) · Springer eBooks · doi:10.1007/978-3-319-23246-1_10 · Cited by 6
Heterogeneous Stocks and Selective Breeding in Aging Research
McClearn, G. E., & McCarter, R. (2011) · ILAR Journal · doi:10.1093/ilar.52.1.16 · Cited by 6
Ikonne, U. S., Vann, P. H., Wong, J. M., Forster, M. J., & Sumien, N. (2018) · Journal of Nutrition · doi:10.1093/jn/nxy287 · Cited by 6
Effects of dietary restriction on genome stability are sex and feeding regimen dependent
Guo, X., Su, F., Gao, Y., Tang, L., Yu, X., Zi, J., Zhou, Y., Wang, H., Xue, J., & Wang, X. (2022) · Food & Function · doi:10.1039/d2fo03138h · Cited by 7
The hidden costs of dietary restriction: implications for its evolutionary and mechanistic originsPreprint
McCracken, A. W., Adams, G., Hartshorne, L., & Simons, M. J. P. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/533711 · Cited by 6
Rapamycin's lifespan effect is modulated by mito‐nuclear epistasis in Drosophila
Ibrahim, R., Martinez, M. B., & Dobson, A. J. (2024) · Aging Cell · doi:10.1111/acel.14328 · Cited by 5
Along the Trajectory to Understanding Cellular Aging: More Lessons from Yeast
Shabestary, K., Dechant, R. C., & Gottschling, D. E. (2025) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev-cellbio-112122-023631 · Cited by 5
Tardif, S. D., & Ross, C. N. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-815962-0.00011-1 · Cited by 6
Mitchell, S. E., Togo, J., Green, C. L., Derous, D., Hambly, C., & Speakman, J. R. (2023) · The Journals of Gerontology Series A · doi:10.1093/gerona/glad152 · Cited by 8
Carr, L. M., Mustafa, S., Care, A., & Collins‐Praino, L. E. (2024) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2024.04.023 · Cited by 5
The circadian rhythm: A key variable in aging?
Winterhalter, P. R., Georgevici, A., Gharpure, N., Szabo, G. B., & Simm, A. (2024) · Aging Cell · doi:10.1111/acel.14268 · Cited by 4
Isolating the direct effects of growth hormone on lifespan and metabolism in mice
Lasher, A. T., Liu, K., Fitch, M. P., & Sun, L. Y. (2024) · Aging Cell · doi:10.1111/acel.14412 · Cited by 6
The impact of co-housing on murine aging studies
Luciano, A., & Churchill, G. A. (2025) · GeroScience · doi:10.1007/s11357-024-01480-x · Cited by 6
Phillips, D., Mathers, H., Mitchell, S. E., & Speakman, J. R. (2022) · The Journals of Gerontology Series A · doi:10.1093/gerona/glac110 · Cited by 5
Fasting and cancer: from yeast to mammals
Tano, M. D., & Longo, V. D. (2022) · International review of cytology · doi:10.1016/bs.ircmb.2022.02.005 · Cited by 6
Extended lifespan in female Drosophila melanogaster through late-life calorie restriction
Li, M., Macro, J., Huggins, B., Meadows, K., Mishra, D., Martin, D., Kannan, K., & Rogina, B. (2024) · GeroScience · doi:10.1007/s11357-024-01233-w · Cited by 5
Restriction de nourriture, longévité et vieillissement
Bourg, É. L. (2011) · Cahiers de Nutrition et de Diététique · doi:10.1016/j.cnd.2011.11.004 · Cited by 5
L’homéostasie métabolique au cœur du vieillissement
Terret, C., & Solari, F. (2012) · médecine/sciences · doi:10.1051/medsci/2012283020 · Cited by 5
Insight into genetic regulation of miRNA in mouse brain
Kordas, G., Rudra, P., Hendricks, A. E., Saba, L. M., & Kechris, K. J. (2019) · BMC Genomics · doi:10.1186/s12864-019-6110-6 · Cited by 5
The Role of Systemic Filtrating Organs in Aging and Their Potential in Rejuvenation Strategies
Kassab, A., Rizk, N. M., & Prakash, S. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23084338 · Cited by 5
Anti-ageing effects of protein restriction unpacked
Hill, C. M., & Kaeberlein, M. R. (2021) · Nature · doi:10.1038/d41586-020-03662-x · Cited by 5
McLachlan, S. M., Aliesky, H. A., Banuelos, B., Magana, J., Williams, R. W., & Rapoport, B. (2014) · Endocrinology · doi:10.1210/en.2014-1388 · Cited by 5
Extension of Life Span in Laboratory Mice
Unnikrishnan, A., Deepa, S. S., Herd, H. R., & Richardson, A. G. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-811353-0.00019-1 · Cited by 7
Mullis, M. N., Wright, K. M., Raj, A., Gatti, D. M., Reifsnyder, P. C., Flurkey, K., Archer, J. R., Robinson, L. L., Francesco, A. D., Svenson, K. L., et al. (2025) · Genetics · doi:10.1093/genetics/iyaf081 · Cited by 6
Neither caloric nor protein restriction increases the male lifespan of outbred short-lived fish
Žák, J., & Reichard, M. (2025) · The Journals of Gerontology Series A · doi:10.1093/gerona/glaf278 · Cited by 4
Lenhart, B. A., Ahsan, A., McHaty, M., & Bergland, A. O. (2024) · Physiological Entomology · doi:10.1111/phen.12443 · Cited by 4
McGill, C. J., Christensen, A., Qian, W., Thorwald, M. A., Godoy-Lugo, J. A., Namvari, S., White, O. S., Finch, C. E., Benayoun, B. A., & Pike, C. J. (2025) · Communications Medicine · doi:10.1038/s43856-025-00942-3 · Cited by 4
MacArthur, M. R., & Mitchell, S. J. (2023) · Current Opinion in Physiology · doi:10.1016/j.cophys.2023.100651 · Cited by 4
A bile acid could explain how calorie restriction slows ageing
Sinclair, D. A. (2024) · Nature · doi:10.1038/d41586-024-04062-1 · Cited by 4
Dietary Restriction: Theory Fails to Satiate—Response
Fontana, L., Partridge, L., & Longo, V. D. (2010) · Science · doi:10.1126/science.329.5995.1015 · Cited by 4
Fridell, Y.-W. C., & Sierra, F. (2018) · Progress in molecular biology and translational science · doi:10.1016/bs.pmbts.2017.12.015 · Cited by 4
Estimating Genetic Variance in Life-Span Response to Diet: Insights From Statistical Simulation
Senior, A. M. (2022) · The Journals of Gerontology Series A · doi:10.1093/gerona/glac172 · Cited by 4
Pappert, F. A., Wüst, V. A., Eguiguren, C. F., & Roth, O. (2025) · Molecular Ecology · doi:10.1111/mec.17754 · Cited by 3
The Promise of a Golden Era for Exploring the Frontiers of Aging, Metabolism and Redox Biology
Zhang, J. (2020) · Frontiers in Aging · doi:10.3389/fragi.2020.610406 · Cited by 4
The damage-independent evolution of ageing by selective destruction
Wordsworth, J., Keefe, H. O., Clark, P. A., & Shanley, D. P. (2022) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2022.111709 · Cited by 4
Genetic analysis of a murine QTL for diet restriction on chromosome 15
Newell‐Stamper, B. L., Kechris, K. J., McQueen, M. B., & Johnson, T. E. (2015) · AGE · doi:10.1007/s11357-014-9740-2 · Cited by 4
Self-citationLongevity as a Complex Genetic Trait
Sutphin, G. L., & Korstanje, R. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-411596-5.00001-0 · Cited by 4
Intragenic repeat expansions control yeast chronological agingPreprint
Barré, B. P., Hallin, J., Yue, J., Persson, K. O., Mikhalev, E., Irizar, A., Thompson, D. A., Molin, M., Warringer, J., & Liti, G. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/653006 · Cited by 4
Mazzetto, M., Reichwald, K., Koch, P., Groth, M., & Cellerino, A. (2025) · The Journals of Gerontology Series A · doi:10.1093/gerona/glae255 · Cited by 3
Godoy-Lugo, J. A., Young, K. E., Vaddi, P., Batamack, Y., Aldridge, J., Fernandez‐Kim, S. O., Albarado, D. C., Burke, S. J., Stephens, J. M., Morrison, C. D., et al. (2025) · GeroScience · doi:10.1007/s11357-025-01853-w · Cited by 4
Ketogenesis is Dispensable for the Metabolic Adaptations to Caloric Restriction
Yeh, C., Borgelt, L., Vogt, B. J., Clark, A. A., Wong, T. T., Grunow, I., Sonsalla, M. M., Babygirija, R., Liu, Y., Trautman, M. E., et al. (2025) · Aging Cell · doi:10.1111/acel.70318 · Cited by 4
Dietary Restriction in C. elegans
Zhang, Y., & Mair, W. B. (2016) · Healthy ageing and longevity · doi:10.1007/978-3-319-44703-2_16 · Cited by 4
Considerations Regarding Public Use of Longevity Interventions
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Metadata
- Authors
- Liao, C., Rikke, B. A., Johnson, T. E., Diaz, V., & Nelson, J. F.
- Affiliations
- The University of Texas at San Antonio Health Science Center (US)
- University of Colorado Boulder (US)
- Corresponding author
- Nelson, James F.
- Venue
- Aging Cell
- Publisher
- Wiley
- Published
- 2010-01-11
- Volume
- 9
- Issue
- 1
- Pages
- 92-95
- ISSN
- 1474-9718 (ISSN-L)
- 1474-9726
- PMC
- PMC3476836
- OpenAlex
- W2104438296
- Cited by
- 501
- References
- 26
- Citations by year
- 2026: 19 · 2025: 25 · 2024: 25 · 2023: 24 · 2022: 32 · 2021: 34 · 2020: 39 · 2019: 33 · 2018: 30 · 2017: 31 · 2016: 41 · 2015: 39 · 2014: 30 · 2013: 31 · 2012: 21
- FWCI
- 6.86
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Aging Cell (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institute on Aging (R01AG024354)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Aging › Genetics, Aging, and Longevity in Model Organisms
- Health Sciences › Medicine › Physiology (medical) › Dietary Effects on Health
- Life Sciences › Agricultural and Biological Sciences › Ecology, Evolution, Behavior and Systematics › Animal Behavior and Reproduction
- Keywords
- dietary restriction, lifespan, genetic variation, recombinant inbred mouse strains, lifespan extension, lifespan reduction, dietary intake, female fertility, sex differences in lifespan, genetic determinants of aging
- MeSH terms
- Animals, Female, Life Expectancy, Longevity, Male, Mice, Inbred Strains, Sex Characteristics, Genetic Variation, Caloric Restriction, Mice
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