Metabolic Networks of Longevity

Resveratrol improves health and survival of mice on a high-calorie diet

Baur, J. A., Pearson, K. J., Price, N. L., Jamieson, H. A., Lerin, C., Kalra, A., Prabhu, V. V., Allard, J. S., Lopez-Lluch, G., Lewis, K., et al. (2006) · Nature · doi:10.1038/nature05354 · Cited by 4,290

Resveratrol Improves Mitochondrial Function and Protects against Metabolic Disease by Activating SIRT1 and PGC-1α

Lagouge, M., Argmann, C., Gerhart-Hines, Z., Meziane, H., Lerin, C., Daussin, F., Messadeq, N., Milne, J., Lambert, P., Elliott, P., et al. (2006) · Cell · doi:10.1016/j.cell.2006.11.013 · Cited by 4,057

Rapamycin fed late in life extends lifespan in genetically heterogeneous mice

Harrison, D. E., Strong, R., Sharp, Z. D., Nelson, J. F., Astle, C. M., Flurkey, K., Nadon, N. L., Wilkinson, J. E., Frenkel, K., Carter, C. S., et al. (2009) · Nature · doi:10.1038/nature08221 · Cited by 3,766

AMPK regulates energy expenditure by modulating NAD+ metabolism and SIRT1 activity

Cantó, C., Gerhart-Hines, Z., Feige, J. N., Lagouge, M., Noriega, L., Milne, J. C., Elliott, P. J., Puigserver, P., & Auwerx, J. (2009) · Nature · doi:10.1038/nature07813 · Cited by 3,300

Extending Healthy Life Span—From Yeast to Humans

Fontana, L., Partridge, L., & Longo, V. D. (2010) · Science · doi:10.1126/science.1172539 · Cited by 3,023

The genetics of ageing

Kenyon, C. J. (2010) · Nature · doi:10.1038/nature08980 · Cited by 2,739

Caloric Restriction Delays Disease Onset and Mortality in Rhesus Monkeys

Colman, R. J., Anderson, R. M., Johnson, S. C., Kastman, E. K., Kosmatka, K. J., Beasley, T. M., Allison, D. B., Cruzen, C., Simmons, H. A., Kemnitz, J. W., et al. (2009) · Science · doi:10.1126/science.1173635 · Cited by 2,277

Induction of autophagy by spermidine promotes longevity

Eisenberg, T., Knauer, H., Schauer, A., Büttner, S., Ruckenstuhl, C., Carmona-Gutierrez, D., Ring, J., Schroeder, S., Magnes, C., Antonacci, L., et al. (2009) · Nature Cell Biology · doi:10.1038/ncb1975 · Cited by 1,680

Absence of S6K1 protects against age- and diet-induced obesity while enhancing insulin sensitivity

Um, S. H., Frigerio, F., Watanabe, M., Picard, F., Joaquin, M., Sticker, M., Fumagalli, S., Allegrini, P. R., Kozma, S. C., Auwerx, J., et al. (2004) · Nature · doi:10.1038/nature02866 · Cited by 1,677

Rates of Behavior and Aging Specified by Mitochondrial Function During Development

Dillin, A., Hsu, A.-L., Arantes-Oliveira, N., Lehrer-Graiwer, J., Hsin, H., Fraser, A. G., Kamath, R. S., Ahringer, J., & Kenyon, C. (2002) · Science · doi:10.1126/science.1077780 · Cited by 1,121

Rewiring yeast acetate metabolism through MPC1 loss of function leads to mitochondrial damage and decreases chronological lifespan

Orlandi, I., Pellegrino-Coppola, D., Vai, M., & Dipartimento di Biotecnologie e Bioscienze, U. D. M.-B. (2014) · Microbial Cell · doi:10.15698/mic2014.12.178 · Cited by 32

Targeting Aging: Lessons Learned From Immunometabolism and Cellular Senescence

Martin, D. E., Torrance, B. L., Haynes, L., & Bartley, J. M. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.714742 · Cited by 29

Common mechanisms for calorie restriction and adenylyl cyclase type 5 knockout models of longevity

Yan, L., Park, J. Y., Dillinger, J., Lorenzo, M. S. D., Yuan, C., Lai, L., Wang, C., Ho, D. W. T., Tian, B., Stanley, W. C., et al. (2012) · Aging Cell · doi:10.1111/acel.12013 · Cited by 29

Forward and reverse genetics approaches to uncover metabolic aging pathways in Caenorhabditis elegans

Gao, A. W., de Bos, J. U., Sterken, M. G., Kammenga, J. E., Smith, R. L., & Houtkooper, R. H. (2017) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2017.09.006 · Cited by 31

Conversions between metabolically unhealthy and healthy obesity from midlife to late-life

Ler, P., Lindfors, E. O., Zhan, Y., Finkel, D., Aslan, A. K. D., & Karlsson, I. (2023) · International Journal of Obesity · doi:10.1038/s41366-023-01425-y · Cited by 31

Accelerated lung aging and chronic obstructive pulmonary disease

Yoon, Y.-S., Jin, M., & Sin, D. D. (2019) · Expert Review of Respiratory Medicine · doi:10.1080/17476348.2019.1580576 · Cited by 26

JNK modifies neuronal metabolism to promote proteostasis and longevity

Wang, L., Davis, S. S., Jensen, M. B., Rodriguez‐Fernandez, I. A., Apaydin, C., Juhász, G., Gibson, B. W., Schilling, B., Ramanathan, A., Ghaemmaghami, S., et al. (2019) · Aging Cell · doi:10.1111/acel.12849 · Cited by 24

Inhibition of the neuromuscular acetylcholine receptor with atracurium activates FOXO/DAF‐16‐induced longevity

McIntyre, R. L., Denis, S. W., Kamble, R., Molenaars, M., Petr, M. A., Schomakers, B. V., Rahman, M., Gupta, S. D., Tóth, M. L., Vanapalli, S. A., et al. (2021) · Aging Cell · doi:10.1111/acel.13381 · Cited by 23

The effect of metformin on influenza vaccine responses in nondiabetic older adults: a pilot trial

Martin, D. E., Cadar, A. N., Panier, H. A., Torrance, B. L., Kuchel, G. A., & Bartley, J. M. (2023) · Immunity & Ageing · doi:10.1186/s12979-023-00343-x · Cited by 25

Cell autonomous and systemic factors in progeria development

Osorio, F. G., Ugalde, A. P., Mariño, G., Puente, X. S., Freije, J. M. P., & López-Otı́n, C. (2011) · Biochemical Society Transactions · doi:10.1042/bst20110677 · Cited by 24

Metabolomics profiling reveals the mechanism of caffeic acid in extending lifespan in Drosophila melanogaster

Li, J., Fang, J., Qin, X., & Gao, L. (2020) · Food & Function · doi:10.1039/d0fo01332c · Cited by 23

Aging and energetics’ ‘Top 40’ future research opportunities 2010-2013

Allison, D. B., Antoine, L. H., Ballinger, S. W., Bamman, M. M., Biga, P. R., Darley-Usmar, V. M., Fisher, G., Gohlke, J. M., Halade, G. V., Hartman, J. L., et al. (2014) · F1000Research · doi:10.12688/f1000research.5212.1 · Cited by 21

Role of mitophagy in the hallmarks of aging

Wen, J., Pan, T., Li, H., Fan, H., Liu, J., Cai, Z., & Zhao, B. (2022) · Journal of Biomedical Research · doi:10.7555/jbr.36.20220045 · Cited by 20

Aging-Related Molecular Pathways in Chronic Cholestatic Conditions

Pinto, C., Ninfole, E., Benedetti, A., Maroni, L., & Marzioni, M. (2020) · Frontiers in Medicine · doi:10.3389/fmed.2019.00332 · Cited by 18

Senoinflammation: A major mediator underlying age-related metabolic dysregulation

Kim, D. H., Bang, E., Arulkumar, R., Ha, S., Chung, K. W., Park, M. H., Choi, Y. J., Yu, B. P., & Chung, H. Y. (2020) · Experimental Gerontology · doi:10.1016/j.exger.2020.110891 · Cited by 19

Comparison of the Prevalence of Cardiometabolic Disorders and Comorbidities in Korea and the United States: Analysis of the National Health and Nutrition Examination Survey

An, S., Ahn, C., Jang, J., Lee, J., Kang, D., Lee, J., & Park, S. K. (2022) · Journal of Korean Medical Science · doi:10.3346/jkms.2022.37.e149 · Cited by 20

Physical exercise elicits UPRmt in the skeletal muscle: The role of c-Jun N-terminal kinase

Gaspar, R. S., Katashima, C. K., Crisol, B., Carneiro, F. S., Sampaio, I. H., Silveira, L. R., da Silva, A. S. R., Cintra, D. E., Pauli, J. R., & Ropelle, E. R. (2023) · Molecular Metabolism · doi:10.1016/j.molmet.2023.101816 · Cited by 20

Metabolites in aging and autophagy

Schroeder, S., Zimmermann, A., Carmona‐Gutiérrez, D., Eisenberg, T., Ruckenstuhl, C., Andryushkova, A., Pendl, T., Harger, A., & Madeo, F. (2014) · Microbial Cell · doi:10.15698/mic2014.04.142 · Cited by 18

Metabolism and chromatin: A dynamic duo that regulates development and ageing

Pouikli, A., & Tessarz, P. (2021) · BioEssays · doi:10.1002/bies.202000273 · Cited by 18

Separation and identification of antioxidant chemical components in Diaphragma juglandis Fructus and functional evaluation in Caenorhabditis elegans

Hong, Q., Geng, S., Ji, J., Ye, Y., Xu, D., Zhang, Y., & Sun, X. (2021) · Journal of Functional Foods · doi:10.1016/j.jff.2021.104422 · Cited by 17

Effects of ketogenic diet containing medium-chain fatty acids on serum inflammatory factor and mTOR signaling pathway in rats

Liu, H., Huang, J., Liu, H., Li, F., Peng, Q., & Liu, C. (2020) · Chemical and Biological Technologies in Agriculture · doi:10.1186/s40538-020-00194-4 · Cited by 16

Nutrient sensing pathways regulating adult reproductive diapause in C. elegans

Eustice, M., Konzman, D., Reece, J. M., Ghosh, S. K., Alston, J. J., Hansen, T. J., Golden, A., Bond, M. R., Abramowitz, L. K., & Hanover, J. A. (2022) · PLoS ONE · doi:10.1371/journal.pone.0274076 · Cited by 16

Chrysin–phospholipid complex-based solid dispersion for improved anti-aging and neuroprotective effects in mice

Salama, A., Elgohary, R., Kassem, A. A., & Asfour, M. H. (2023) · Pharmaceutical Development and Technology · doi:10.1080/10837450.2023.2165102 · Cited by 16

A metabolomic signature of decelerated physiological aging in human plasma

Janssens, G. E., Grevendonk, L., Schomakers, B. V., Perez, R. Z., van Weeghel, M., Schrauwen, P., Hoeks, J., & Houtkooper, R. H. (2023) · GeroScience · doi:10.1007/s11357-023-00827-0 · Cited by 15

Developmental drift as a mechanism for aging: lessons from nematodes

Lezzerini, M., Smith, R. L., & Budovskaya, Y. V. (2013) · Biogerontology · doi:10.1007/s10522-013-9462-3 · Cited by 16

Crosstalk between Lipid Rafts and Aging: New Frontiers for Delaying Aging

Zhang, S., Zhu, N., Gu, J., Li, H., Qiu, Y., Liao, D.-F., & Li, Q. (2022) · Aging and Disease · doi:10.14336/ad.2022.0116 · Cited by 16

Deciphering hallmark processes of aging from interaction networks

Smita, S., Lange, F., Wolkenhauer, O., & Köhling, R. (2016) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2016.07.017 · Cited by 15

Links between telomere dysfunction and hallmarks of aging

Li, S., Liu, Z., Zhang, J., & Li, L. (2023) · Mutation Research/Genetic Toxicology and Environmental Mutagenesis · doi:10.1016/j.mrgentox.2023.503617 · Cited by 15

Regulation and mechanism of Bletilla striata polysaccharide on delaying aging in Drosophila melanogaster

Hafeez, E., Du, D., Ni, H., Zhu, K., Hu, F., Zhou, J., & Chen, D. (2025) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2025.143382 · Cited by 14

Plasma methionine metabolic profile is associated with longevity in mammals

Mota‐Martorell, N., Jové, M., Berdún, R., & Pamplona, R. (2021) · Communications Biology · doi:10.1038/s42003-021-02254-3 · Cited by 16

Sirtuin 1 (SIRT1) and Oxidative Stress

Li, H. (2014) · Springer eBooks · doi:10.1007/978-3-642-30018-9_17 · Cited by 16

RNA-seq profiling, and impaired autophagic process in skeletal muscle of MELAS

Deng, J., Lu, Y., Xie, Z., Liu, J., Yuan, Y., & Wang, Z. (2019) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2019.12.005 · Cited by 14

Hyperactive mTORC1/4EBP1 signaling dysregulates proteostasis and accelerates cardiac aging

Zarzycka, W., Kobak, K. A., King, C. J., Peelor, F. F., Miller, B. F., & Chiao, Y. A. (2024) · GeroScience · doi:10.1007/s11357-024-01368-w · Cited by 12

Epigenetics and Aging

Soriano‐Tárraga, C., Jiménez-Conde, J., & Roquer, J. (2019) · Springer eBooks · doi:10.1007/978-3-319-55530-0_123 · Cited by 15

Gene Duplication and Phenotypic Changes in the Evolution of Mammalian Metabolic Networks

Bekaert, M., & Conant, G. C. (2014) · PLoS ONE · doi:10.1371/journal.pone.0087115 · Cited by 12

Genetic perturbation of key central metabolic genes extends lifespan in Drosophila and affects response to dietary restriction

Talbert, M. E., Barnett, B., Hoff, R., Amella, M., Kuczynski, K., Lavington, E., Koury, S. A., Brud, E., & Eanes, W. F. (2015) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2015.1646 · Cited by 12

Sirtuin-dependent recovery from aerial heat shock: The effects of food ration, thermal history, and sirtuin inhibition on clearance rates and valve gape activity of the California mussel, Mytilus californianus (Conrad)

May, M., Feezell, M. K., Gonzalez, S. J., Vasquez, M. C., Todgham, A. E., & Tomanek, L. (2021) · Journal of Experimental Marine Biology and Ecology · doi:10.1016/j.jembe.2020.151510 · Cited by 14

Poly (ADP-ribose) polymerase1 regulates growth and multicellularity in D. discoideum

Jubin, T., Kadam, A. A., Saran, S., & Begum, R. (2016) · Differentiation · doi:10.1016/j.diff.2016.03.002 · Cited by 11

Inositol Polyphosphate Multikinase (IPMK), a Gene Coding for a Potential Moonlighting Protein, Contributes to Human Female Longevity

Rango, F. D., Crocco, P., Iannone, F., Saiardi, A., Passarino, G., Dato, S., & Rose, G. (2019) · Genes · doi:10.3390/genes10020125 · Cited by 9

Ketogenic Diet Consumption Inhibited Mitochondrial One-Carbon Metabolism

Hsu, F.-Y., Liou, J.-Y., Tang, F., Sou, N., Peng, J.-H., & Chiang, E. I. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23073650 · Cited by 10

The whole transcriptome regulation as a function of mitochondrial polymorphisms and aging in Caenorhabditis elegans

Song, Y., Wang, Y., Li, Y., Wang, L., Zhang, W., Cheng, J., Zhu, Y., Zhang, H., Zhang, Q., Niu, H., et al. (2020) · Aging · doi:10.18632/aging.102754 · Cited by 11

Insights into the functional aspects of poly(ADP‐ribose) polymerase‐1 (PARP‐1) in mitochondrial homeostasis in Dictyostelium discoideum

Kadam, A. A., Jubin, T., Roychowdhury, R., Garg, A., PARMAR, N. R., Palit, S. P., & Begum, R. (2020) · Biology of the Cell · doi:10.1111/boc.201900104 · Cited by 11

WITHDRAWN: Nuclear matrix, nuclear envelope and premature aging syndromes in a translational research perspective

Cau, P., Navarro, C. L., Harhouri, K., Roll, P., Sigaudy, S., Kaspi, É., Perrin, S., Sandre‐Giovannoli, A. D., & Lévy, N. (2014) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2014.03.022 · Cited by 10

Can accelerated ageing models inform us on age‐related tauopathies?

Han, Z. Z., Fleet, A., & Larrieu, D. (2023) · Aging Cell · doi:10.1111/acel.13830 · Cited by 10

Greater Phosphorylation of AMPK and Multiple AMPK Substrates in the Skeletal Muscle of 24-Month-Old Calorie Restricted Compared to Ad-Libitum Fed Male Rats

Zheng, A., Kwak, S. E., Birk, J. B., Arias, E. B., Thorley, D., Wojtaszewski, J. F. P., & Cartee, G. D. (2022) · The Journals of Gerontology Series A · doi:10.1093/gerona/glac218 · Cited by 9

The Influence of Shc Proteins and Aging on Whole Body Energy Expenditure and Substrate Utilization in Mice

Stern, J. H., Kim, K., & Ramsey, J. J. (2012) · PLoS ONE · doi:10.1371/journal.pone.0048790 · Cited by 8

Bioavailability and Biological Effects of 2-O-β- d -Glucopyranosyl-carboxyatractyligenin from Green Coffee in Caenorhabditis elegans

Spanier, B., Lang, R., Weber, D. D., Lechner, A., Thoma, T., Rothner, M., Petzold, K., Lang, T., Beusch, A., Bösl, M., et al. (2019) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.8b06785 · Cited by 8

Review on potential of Caenorhabditis Elegans as an anti-aging evaluation model for polysaccharides

Zheng, H., Su, C., Zi, W., Zhao, L., & Li, W. (2025) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2025.146921 · Cited by 9

Underlying Mechanisms of the Protective Effects of Lifestyle Factors On Age-Related Diseases

Alcaraz, N., Salcedo‐Tello, P., González‐Barrios, R., Torres‐Arciga, K., & Guzmán-Ramos, K. R. (2024) · Archives of Medical Research · doi:10.1016/j.arcmed.2024.103014 · Cited by 9

The rosetta stone of successful ageing: does oral health have a role?

Poser, M., Sing, K. E. A., Ebert, T., Ziebolz, D., & Schmalz, G. (2023) · Biogerontology · doi:10.1007/s10522-023-10047-w · Cited by 7

Reduced ech-6 expression attenuates fat-induced lifespan shortening in C. elegans

Liu, Y. J., Gao, A. W., Smith, R. L., Janssens, G. E., Panneman, D. M., Jongejan, A., van Weeghel, M., Vaz, F. M., Silvestrini, M. J., Lapierre, L. R., et al. (2022) · Scientific Reports · doi:10.1038/s41598-022-07397-9 · Cited by 7

Cellular Mechanisms of Age-Related Hearing Loss

Melgar–Rojas, P., Alvarado, J. C., Fuentes‐Santamaría, V., & Juiz, J. M. (2015) · Oxidative stress in applied basic research and clinical practice · doi:10.1007/978-3-319-13473-4_15 · Cited by 6

Plausible Links Between Metabolic Networks, Stem Cells, and Longevity

Kucia, M., & Ratajczak, M. Z. (2019) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-31206-0_15 · Cited by 6

The influence of acute, late-life calorie restriction on whole body energy metabolism in p66Shc(−/−) mice

Stern, J. H., Kim, K., & Ramsey, J. J. (2012) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2012.05.001 · Cited by 6

Gut microbiome synthesizes important core metabolites to prevent cognitive decline and mitigate onset and progression of Alzheimer's disease

Al-Abbas, N. S., & Shaer, N. A. (2024) · Journal of Alzheimer s Disease Reports · doi:10.1177/25424823241309024 · Cited by 5

New views on the selection acting on genetic polymorphism in central metabolic genes

Eanes, W. F. (2016) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.13285 · Cited by 7

Multi-dimensional computational pipeline for large-scale deep screening of compound effect assessment: an in silico case study on ageing-related compounds

Gupta, V., Crudu, A., Matsuoka, Y., Ghosh, S., Rozot, R., Marat, X., Jäger, S., Kitano, H., & Breton, L. (2019) · npj Systems Biology and Applications · doi:10.1038/s41540-019-0119-y · Cited by 5

Uncovering the roles of sirtuin activity and food availability during the onset of the heat shock response in the California mussel (Mytilus californianus): Implications for antioxidative stress responses

May, M., & Tomanek, L. (2023) · Comparative Biochemistry and Physiology Part B Biochemistry and Molecular Biology · doi:10.1016/j.cbpb.2023.110902 · Cited by 7

Resveratrol: A Sirtuin Activator and The Fountain of Youth

Meiliana, A., Dewi, N. M., & Wijaya, A. (2015) · The Indonesian Biomedical Journal · doi:10.18585/inabj.v7i1.16 · Cited by 4

Glucose and cholesterol induce abnormal cell divisions via DAF-12 and MPK-1 in C. elegans

Qu, Z., Ji, S., & Zheng, S. (2020) · Aging · doi:10.18632/aging.103647 · Cited by 5

Reduction of halocarbons to hydrocarbons by NADH models and NADH

Denk, M. K., Milutinović, N. S., & Dereviankin, M. Y. (2019) · Chemosphere · doi:10.1016/j.chemosphere.2019.05.169 · Cited by 5

Proteomic analysis of plasma after branched chain enriched mixture supplementation in mice

Brocca, L., Mascaro, A., & D’Antona, G. (2013) · Journal of the International Society of Sports Nutrition · doi:10.1186/1550-2783-10-19 · Cited by 4

The Interaction between Metabolic Disease and Ageing

Rana, K. S., Griffiths, H. R., Placido, N., & Brown, J. E. P. (2014) · Global Journal of Obesity Diabetes and Metabolic Syndrome · doi:10.17352/2455-8583.000002 · Cited by 4

Metabolic elasticity: A new measure of age

Bennett, S. E., & Sato, S. (2023) · Cell Metabolism · doi:10.1016/j.cmet.2023.08.006 · Cited by 3

Stem Cell Aging

Rožman, P. J., Jazbec, K., & Jež, M. (2018) · InTech eBooks · doi:10.5772/intechopen.71764 · Cited by 4

Nutritional Influences on Epigenetics, Aging and Disease

Meiliana, A., Dewi, N. M., & Wijaya, A. (2019) · The Indonesian Biomedical Journal · doi:10.18585/inabj.v11i1.780 · Cited by 3

MOLECULAR MECHANISMS OF STEM CELL AGING

Jazbec, K., Jež, M., Justin, M., & Rožman, P. J. (2019) · Slovenian Veterinary Research · doi:10.26873/svr-545-2018 · Cited by 7

Mitochondria at the heart of aging: structure, function, and failure

Marei, H. E. S. (2026) · Journal of Translational Medicine · doi:10.1186/s12967-026-08047-8 · Cited by 7

The Association of Macronutrient Consumption and BMI to Exhaled Carbon Dioxide in Lumen Users: Retrospective Real-World Study

Yeshurun, S., Cramer, T., Souroujon, D., & Mor, M. (2024) · JMIR mhealth and uhealth · doi:10.2196/56083 · Cited by 2

The Influence of Shc Proteins on the Whole Body Energetic Response to Calorie Restriction Initiated in 3-Month-Old Mice

Stern, J. H., Kim, K., & Ramsey, J. J. (2014) · ISRN Nutrition · doi:10.1155/2014/562075 · Cited by 2

Sirtuins and Aging

Cantó, C., & Houtkooper, R. H. (2016) · Springer eBooks · doi:10.1007/978-94-024-0962-8_10 · Cited by 2

The potential longevity-promoting hypoxic-hypercapnic environment as a measure for radioprotection

David, E., Wolfson, M., Muradian, K. K., & Fraifeld, V. E. (2024) · Biogerontology · doi:10.1007/s10522-024-10129-3 · Cited by 3

Novel plant bioactives, their antiaging potencies: reality and promises

Kuppusamy, U. R., & Arumugam, B. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-90581-7.00020-7 · Cited by 1

مکانیسمهای سلولی مولکولی اثرات رزوراترول در قلب وعروق

هاشمیان, م., & زند, ح. (2015) · مجله علمی دانشگاه علوم پزشکی بابل · doi:10.22088/jbums.17.4.51 · Cited by 1

Contrôle de la signalisation et de l’action de l’insuline par la protéine Grb14

Gondoin, A., Morzyglod, L., Desbuquois, B., & Burnol, A. (2014) · Biologie Aujourd hui · doi:10.1051/jbio/2014013 · Cited by 1

SIRT7: from a Metabolic Regulator to a Disease Marker

Lin, Z. (2015) · International Journal of Cancer Studies & Research · doi:10.19070/2167-9118-150009 · Cited by 1

Aging in Rodents

Navarro, H. G., Doğan, S., Tuna, B. G., Potter, P. K., Kõks, G., & Kõks, S. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-801238-3.11433-3 · Cited by 1

Molecular Signature of Aging Driven by Wnt Signaling Pathway: Lessons from Nematodes

Lezzerini, M., & Budovskaya, Y. V. (2019) · Healthy ageing and longevity · doi:10.1007/978-3-030-24970-0_22 · Cited by 1

Epigenetics and Aging

Soriano‐Tárraga, C., Jiménez-Conde, J., & Roquer, J. (2018) · Springer eBooks · doi:10.1007/978-3-319-31143-2_123-1 · Cited by 1

Western-style diet does not negatively affect the healthy aging benefits of lifelong restrictive feeding

Reijne, A. C., Talarovičová, A., Coolen, A., Bruggink, J. E., Čiapaitė, J., Bleeker, A., Groen, A. K., Reijngoud, D., Bakker, B. M., & van Dijk, G. (2022) · Nutrition and Healthy Aging · doi:10.3233/nha-220163 · Cited by 2

Nutrition in the Elderly

Mocchegiani, E. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-801816-3.00005-4 · Cited by 1

Can Autophagy Stop the Clock: Unravelling the Mystery in Dictyostelium discoideum

Sharma, P., Jain, P., Shrivastava, A., & Saran, S. (2020) · Springer eBooks · doi:10.1007/978-981-32-9005-1_13 · Cited by 1

EFEK YOGA TERHADAP KOMPONEN BIOMOLEKULAR PADA PROSES CELL AGING

Wahyuni, N. (2020) · Sport and Fitness Journal · doi:10.24843/spj.2020.v08.i02.p03 · Cited by 1

Natural genetic variation in C. elegans reveals genomic loci controlling metabolite levelsPreprint

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