Essential role for autophagy in life span extension

The Hallmarks of Aging

López-Otín, C., Blasco, M. A., Partridge, L., Serrano, M., & Kroemer, G. (2013) · Cell · doi:10.1016/j.cell.2013.05.039 · Cited by 14,982

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

Autophagy regulates lipid metabolism

Singh, R., Kaushik, S., Wang, Y., Xiang, Y., Novak, I., Komatsu, M., Tanaka, K., Cuervo, A. M., & Czaja, M. J. (2009) · Nature · doi:10.1038/nature07976 · Cited by 3,975

Small molecule activators of sirtuins extend Saccharomyces cerevisiae lifespan

Howitz, K. T., Bitterman, K. J., Cohen, H. Y., Lamming, D. W., Lavu, S., Wood, J. G., Zipkin, R. E., Chung, P., Kisielewski, A., Zhang, L.-L., et al. (2003) · Nature · doi:10.1038/nature01960 · Cited by 3,796

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

Bcl-2 Antiapoptotic Proteins Inhibit Beclin 1-Dependent Autophagy

Pattingre, S., Tassa, A., Qu, X., Garuti, R., Liang, X. H., Mizushima, N., Packer, M., Schneider, M. D., & Levine, B. (2005) · Cell · doi:10.1016/j.cell.2005.07.002 · Cited by 3,536

The Beclin 1 network regulates autophagy and apoptosis

Kang, R., Zeh, H. J., Lotze, M. T., & Tang, D. (2011) · Cell Death & Differentiation · doi:10.1038/cdd.2010.191 · Cited by 2,485

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

Autophagosome formation: core machinery and adaptations

Xie, Z., & Klionsky, D. J. (2007) · Nature Cell Biology · doi:10.1038/ncb1007-1102 · Cited by 2,237

Autophagy and Aging

Rubinsztein, D. C., Mariño, G., & Kroemer, G. (2011) · Cell · doi:10.1016/j.cell.2011.07.030 · Cited by 2,107

Influences of Germline Cells on Organismal Lifespan and Healthspan

Amrit, F. R. G., & Ghazi, A. (2016) · Healthy ageing and longevity · doi:10.1007/978-3-319-44703-2_6 · Cited by 6

Quantification of Autophagy During Senescence

Park, J. T., Lee, Y., & Park, S. C. (2018) · Methods in molecular biology · doi:10.1007/978-1-4939-8931-7_14 · Cited by 6

Autophagy - how to control your intracellular diet

Tschachler, E., & Eckhart, L. (2017) · British Journal of Dermatology · doi:10.1111/bjd.15566 · Cited by 7

Effect of selenium on the cellular structure and oxidative response of the yeasts Saccharomyces cerevisiae and Rhodotorula glutinis

Sęk, W., Lisiecka, U., Ostrowska, A., & Kieliszek, M. (2026) · Journal of Trace Elements in Medicine and Biology · doi:10.1016/j.jtemb.2026.127843 · Cited by 6

Grp94 Inhibitor HCP1 Inhibits Human Dermal Fibroblast Senescence

Cui, X., Hao, X., Wen, J., Zhang, S., Zhao, B., & Miao, J. (2022) · Genes · doi:10.3390/genes13091651 · Cited by 6

Autophagy and Cellular Senescence in Lung Diseases

Kuwano, K., Araya, J., Hara, H., Minagawa, S., Takasaka, N., Ito, S., & Nakayama, K. (2015) · Journal of Biochemistry and Molecular Biology Research · doi:10.17554/j.issn.2313-7177.2015.01.5 · Cited by 6

Autophagy in kidney transplants of sirolimus treated recipients

Bhayana, S., Baisantry, A., Kraemer, T. D., Wrede, C., Hegermann, J., Bräsen, J. H., Bockmeyer, C. L., Becker, J. U., Ochs, M., Gwinner, W., et al. (2016) · Journal of Nephropathology · doi:10.15171/jnp.2017.15 · Cited by 6

Autophagic cell death in viral infection: Do TAM receptors play a role?

Datan, E., & Salman, S. (2020) · International review of cytology · doi:10.1016/bs.ircmb.2020.10.001 · Cited by 5

Relating aging and autophagy – a new perspective towards the welfare of human health

Chowdhury, S. G., Ray, R., & Karmakar, P. (2023) · EXCLI journal · doi:10.17179/excli2023-6300 · Cited by 8

The Role of Epithelial Cell Quality Control in Health and Disease of the Distal Lung

Beers, M. F., Nureki, S., & Mulugeta, S. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-803809-3.00008-7 · Cited by 7

Plasminogen activator inhibitor 1 promotes aortic aging–like pathophysiology in humans and mice

Khoddam, A., Kalousdian, A., Eren, M., Soberanes, S., Decker, A., Lux, E., Zywicki, B. W., Dinh, B., Boztepe, B., Cheema, B. S., et al. (2025) · Journal of Clinical Investigation · doi:10.1172/jci196714 · Cited by 6

Proteostasis of organelles in aging and disease

Nabawi, Y., Doğan, C., Petrovic, D., Perçin, G. I., Koyuncu, S., & Vílchez, D. (2026) · FEBS Journal · doi:10.1111/febs.70439 · Cited by 6

The role of spermidine in plants and humans: a pathway from climate change adaptation to health benefits

Blagojević, B., Brunel‐Muguet, S., Šućur, R., Mladenov, V., Balaž, I., Vollmann, J., Fotopoulos, V., & Mäder, K. (2026) · npj Science of Food · doi:10.1038/s41538-025-00695-2 · Cited by 5

Transcriptional and epigenetic regulation of autophagy: mechanisms, disease relevance and therapeutic opportunities

Seo, J., Park, S., Lee, D. C., Yoo, W., Yang, Y. R., Seo, H. W., Park, J. L., Joo, J., Park, K. C., & Byun, S. (2026) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-026-02688-3 · Cited by 5

Biomolecular Markers of Brain Aging

Li, M., An, H., Wang, W., & Wei, D. (2023) · Advances in experimental medicine and biology · doi:10.1007/978-981-99-1627-6_9 · Cited by 7

X-rays and metformin cause increased urinary excretion of cell-free nuclear and mitochondrial DNA in aged rats

Gaziev, A. I., Abdullaev, S. A., Minkabirova, G., & Kamenskikh, K. A. (2016) · Journal of Circulating Biomarkers · doi:10.1177/1849454416670782 · Cited by 5

Inhibitor of growth protein 4 interacts with Beclin 1 and represses autophagy

Sica, V., Pedro, J. M. B., Chen, G., Mariño, G., Lachkar, S., Izzo, V., Maiuri, M. C., Niso‐Santano, M., & Kroemer, G. (2017) · Oncotarget · doi:10.18632/oncotarget.19033 · Cited by 5

Pathogen-Induced Hormetic Responses

Jentho, E., Lajqi, T., Yang, K., Winkler, R., Stojiljkovic, M. R., Wetzker, R., & Bauer, M. W. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-814253-0.00014-0 · Cited by 5

Genes acting in longevity‐related pathways in the endoparasitoid, Pteromalus puparum

Xiong, S., Yu, K., Ye, X., Fang, Q., Deng, Y., Xiao, S., Yang, L., Wang, B., Wang, F., Yan, Z., et al. (2019) · Archives of Insect Biochemistry and Physiology · doi:10.1002/arch.21635 · Cited by 5

dCubilin/dAMN- mediated protein reabsorption in Drosophila nephrocytes modulates longevity

Feng, X., Hong, X., Fan, Q., Chen, L., Li, J., Deng, J., Gong, S., Hou, F. F., & Zhang, F. (2021) · Disease Models & Mechanisms · doi:10.1242/dmm.047464 · Cited by 5

Autophagy stimulation delayed biological aging and decreased cardiac differentiation in rabbit mesenchymal stem cells

Hassanpour, M., Cheraghi, O., Rahbarghazi‬, R., & Nouri, M. (2021) · Journal of Cardiovascular and Thoracic Research · doi:10.34172/jcvtr.2021.43 · Cited by 5

Autophagy promotes longevity—except in the presence of ‘leaky’ mitochondria

Abdellatif, M. (2019) · Cardiovascular Research · doi:10.1093/cvr/cvz224 · Cited by 5

Natural Products in the Promotion of Healthspan and Longevity.

Niso‐Santano, M., González‐Polo, R. A., Paredes-Barquero, M., Fuentes, J. M., & Aschner, M. (2019) · PubMed · doi:10.31700/2572-7656.000123 · Cited by 5

Redox Signalling, Autophagy and Ageing

Hussain, F., Warraich, U.-E.-A., & Jamil, A. (2021) · Healthy ageing and longevity · doi:10.1007/978-3-030-84965-8_7 · Cited by 5

Potential of Lambda-Cyhalothrin for Controlling the Black Armyworm Spodoptera cosmioides (Walker) (Lepidoptera: Noctuidae): Toxicity and Midgut Histopathological Effects

Rocha, F. A. D., Martínez, L. C., Lima, B. S. A., Farder-Gomes, C. F., Cossolin, J. F. S., Afzal, M. B. S., & Serrão, J. É. (2025) · Neotropical Entomology · doi:10.1007/s13744-024-01236-4 · Cited by 4

Healthy Aging

Casey, C., & Seidman, M. D. (2022) · Otolaryngologic Clinics of North America · doi:10.1016/j.otc.2022.06.016 · Cited by 8

Autophagy Alterations in White and Brown Adipose Tissues of Mice Exercised under Different Training Protocols

Tamargo‐Gómez, I., Fernández‐Sanjurjo, M., Codina‐Martínez, H., Tomás‐Zapico, C., Iglesias‐Gutiérrez, E., Fernández, Á. F., & Fernández, Á. F. (2024) · Frontiers in Bioscience-Landmark · doi:10.31083/j.fbl2910348 · Cited by 4

L’autophagie, l’homéostasie intestinale et ses pathologies

Trentesaux, C., Fraudeau, M., & Romagnolo, B. (2017) · médecine/sciences · doi:10.1051/medsci/20173303016 · Cited by 4

Physical Activity As a Preventive Measure against Cardiovascular Disease in Elderly Patients

Kotovskaya, Y. V., Tkacheva, O. N., Рунихина, Н. К., & Вячеславовна, Л. А. (2019) · Doctor Ru · doi:10.31550/1727-2378-2019-157-2-19-22 · Cited by 8

Aging and Protein Kinases

Engin, A. B., & Engin, A. (2021) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-49844-3_2 · Cited by 4

Role and Molecular Mechanisms of Lysosomes and Cathepsins in Neuropathology and Aging: New Insights

Khawar, M. B., Naz, F., Hassan, A. M., Sheikh, N., Nabeela, A. H., Rabia, M., Maryam, M., Arif, A., Zaira, A., Zerwa, S., et al. (2021) · Journal of Neurodegenerative Disorders · doi:10.36959/459/605 · Cited by 3

Sit4 Genetically Interacts with Vps27 to Regulate Mitochondrial Function and Lifespan in Saccharomyces cerevisiae

Martins, T. S., Correia, M., Pinheiro, D., Lemos, C., Mendes, M. V., Pereira, C., & Costa, V. (2024) · Cells · doi:10.3390/cells13080655 · Cited by 3

Energy deprivation in youth and old age

Stern, M. (2025) · Journal of Cell Science · doi:10.1242/jcs.264018 · Cited by 3

NAD+ Homeostasis and Autophagy: Integrated Control Through Nutrient Signaling in Yeast and Mammals

McDaniel, M., Lee, L.-H., & Lin, S.-J. (2025) · Cells · doi:10.3390/cells14191495 · Cited by 4

High-Spermidine-Producing Yeast Strain for Autophagy-Promoting Applications

Koshizawa, T., Numaguchi, T., Tamakoshi, M., Sato, Y., Hashimoto, K., Ishak, N. S. M., & Ikemoto, K. (2025) · Processes · doi:10.3390/pr13103141 · Cited by 4

Autoimmunity, diet and autophagy

Blaise, S. A., & Muller, S. (2026) · Autoimmunity Reviews · doi:10.1016/j.autrev.2026.104040 · Cited by 3

Deciphering the role of SIRT6 in suppressing the AMPK-mTOR-TFEB axis: regulation of autophagy activation in HCC

Li, C. S., Jin, H., Meng, R., Baek, S.-W., Kim, S., Chai, O. H., Park, B. H., Lee, N. R., Kim, S. M., & Kim, S. M. (2026) · Cancer Gene Therapy · doi:10.1038/s41417-026-01023-w · Cited by 3

Decreased expression of autophagy markers in culture-positive patients with chronic otitis media

Jung, J., Park, D. C., Kim, Y. I., Lee, E. H., Park, M. J., Kim, S. H., & Yeo, S. G. (2020) · Journal of International Medical Research · doi:10.1177/0300060520936174 · Cited by 3

High throughput screening for autophagy

Forveille, S., Leduc, M., Sauvat, A., Cerrato, G., Kroemer, G., & Kepp, O. (2021) · Methods in cell biology · doi:10.1016/bs.mcb.2020.12.011 · Cited by 3

Mitochondrial modulators

Naumova, N., Koliada, A. K., Kuzub, N., & Vaiserman, A. M. (2023) · Elsevier eBooks · doi:10.1016/b978-0-12-823679-6.00012-6 · Cited by 3

Improving our understanding of the biology of aging: findings from the Age-It Research Program

Chiti, F., Conti, F., Corda, D., Giorgino, F., Graziani, A., Passarino, G., Sandri, M., & di Fagagna, F. D. (2025) · The Journals of Gerontology Series B · doi:10.1093/geronb/gbaf197 · Cited by 4

Autophagie, bonne santé et longévité

Galluzzi, L., Pedro, J. M. B., & Kroemer, G. (2017) · médecine/sciences · doi:10.1051/medsci/20173303010 · Cited by 4

Aging in the Nematode Caenorhabditis elegans

Daskalaki, I., Markaki, M., & Tavernarakis, N. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-801238-3.11376-5 · Cited by 4

Dynamic modulation of autophagy: implications for aging and cancer

Cassidy, L. D., & Narita, M. (2020) · Molecular & Cellular Oncology · doi:10.1080/23723556.2020.1754723 · Cited by 3

Dietary Polyphenols in Aging: A Systems-Level Perspective on Mitochondrial Quality Control and Microbiome Interactions

Yılmaz, A., Park, H.-J., Ahn, E., & Bae, J. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27093930 · Cited by 4

The role of intermittent fasting in modulating oxidative stress: a narrative review

Raja, P. A. L., Gunadi, J. W., & Sanjaya, A. (2026) · Molecular Biology Reports · doi:10.1007/s11033-026-12142-w · Cited by 3

Endoplasmic Reticulum Stress of Skeletal Muscle and Exercise Training Effects in Aging and Obesity

Ahn, N., Koh, J., & Kim, K. (2018) · The Asian Journal of Kinesiology · doi:10.15758/ajk.2018.20.3.1 · Cited by 2

Autophagy in germ cells, stem cells, and induced pluripotent stem cells

Islam, M., Nguyen, N. U. N., Diwan, A., & Rothermel, B. A. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-822003-0.00028-0 · Cited by 2

The Physiological Adaptation Features of the Poly-Extremophilic Yeast Yarrowia lipolytica W29 During Long-Term Cultivation

Гесслер, Н. Н., Ivanova, N. O., Kokoreva, A. S., Klein, O. I., Isakova, E. P., & Deryabina, Y. I. (2022) · Applied Biochemistry and Microbiology · doi:10.1134/s0003683822060047 · Cited by 2

Roles of poly(ADP-ribose) polymerase 1 and mitophagy in progeroid syndromes as well as physiological ageing

Suga, N., Ikeda, Y., Yoshikawa, S., & Matsuda, S. (2023) · Exploration of Medicine · doi:10.37349/emed.2023.00180 · Cited by 2

The role of different physical exercises as an anti-aging factor in different stem cells

Xu, J., & Song, Z. (2025) · Biogerontology · doi:10.1007/s10522-025-10205-2 · Cited by 3

Monitoring the Biological Impact and Therapeutic Potential of Intermittent Fasting in Oncology: Assessing Strategies and Clinical Translational Challenges

Bendykowska, M., & Gromadzka, G. (2025) · Diagnostics · doi:10.3390/diagnostics15182369 · Cited by 4

Regulation of Macroautophagy by Nutrients and Metabolites

Lorin, S., Pattingre, S., Meijer, A. J., & Codogno, P. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-802167-5.00014-1 · Cited by 2

Zinc, Insulin and IGF-I Interplay in Aging

Malavolta, M., Piacenza, F., Costarelli, L., Cardelli, M., Santarelli, L., Mocchegiani, E., Basso, A., Pierpaoli, E., Provinciali, M., & Giacconi, R. (2017) · Healthy ageing and longevity · doi:10.1007/978-3-319-63001-4_4 · Cited by 2

CK1α promotes tumour suppressive autophagy

Heřmanová, I., & Carracedo, A. (2018) · Nature Cell Biology · doi:10.1038/s41556-018-0079-2 · Cited by 2

Overview of Autophagy

Hayat, M. A. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-805420-8.00001-9 · Cited by 3

Identification of putative calorie restriction mimetics using mammalian gene expression profiles

Vázquez, A. (2020) · Open Biology · doi:10.1098/rsob.200158 · Cited by 2

The Basics of Biogerontology

Rinnerthaler, M., & Richter, K. (2018) · InTech eBooks · doi:10.5772/intechopen.76246 · Cited by 2

The anti-aging mechanism of Berberine associated with metabolic control

Guo, X., Xiong, X., Lijun, Z., Zhong, G., & Zhu, X. (2023) · Elsevier eBooks · doi:10.1016/b978-0-12-823679-6.00020-5 · Cited by 1

Diet-mediated bioenergetic flux: a double-edged sword for health and diseases

Nasb, M., Luo, A., Dayoub, L., Wang, M., & Chen, N. (2025) · Food Science and Human Wellness · doi:10.26599/fshw.2025.9250724 · Cited by 2

A new vision of Panax ginseng leaf polysaccharide function: multiple roles in improving growth, flesh quality and muscle energy metabolism of sub-adult grass carp (Ctenopharyngodon idella)

Yang, J., Wu, P., Jiang, W., Liu, Y., Ma, Y.-B., Jin, X., Ren, H., Shi, H.-Q., Zhou, X., & Feng, L. (2025) · Journal of Animal Science and Biotechnology/Journal of animal science and biotechnology · doi:10.1186/s40104-025-01256-z · Cited by 1

Autophagy in lipid metabolism

Sekar, M., & Thirumurugan, K. (2025) · Advances in clinical chemistry · doi:10.1016/bs.acc.2025.10.007 · Cited by 1

Geroprotective effects of Salvianolic acid A through redox and detoxification pathway activation in an aging Drosophila Alzheimer’s model

Tan, F. H. P., Najimudin, N., Azzam, G., Zainuddin, A., Shamsuddin, S., & Kasihmuddin, M. S. M. (2026) · Biogerontology · doi:10.1007/s10522-026-10388-2 · Cited by 1

Autophagy: A Double-Edged Sword in the Aging of C. elegans

Sigmond, T., & Barna, J. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27083488 · Cited by 2

Anhydrobiosis as a Model of Aging and Longevity: The Role of Autophagy and Metabolism in Yeast Cells

Jonnagiri, N. P. K. R., & Kieliszek, M. (2026) · Microbial Ecology · doi:10.1007/s00248-026-02782-7 · Cited by 1

Microbiome−host proteostasis crosstalk—An emerging perspective on mechanisms and interventions toward healthy longevity

Dubey, A. A., & Ermolaeva, M. (2026) · FEBS Letters · doi:10.1002/1873-3468.70386 · Cited by 1

Pathogenesis of COPD 4 – Cell Death, Senescence, and Autophagy: Is There a Possibility of Developing New Drugs from the Standpoint of This Pathogenetic Mechanism?

Kuwano, K., Araya, J., Hara, H., Minagawa, S., Takasaka, N., Ito, S., & Nakayama, K. (2016) · Respiratory disease series · doi:10.1007/978-981-10-0839-9_6 · Cited by 1

Anti-Aging Drugs

Vaiserman, A. M. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-409547-2.12295-4 · Cited by 1

Brain Aging in HIV-1 Infection

Santerre, M., & Sawaya, B. E. (2018) · IntechOpen eBooks · doi:10.5772/intechopen.77029 · Cited by 1

Autophagic processes of normal and malignant metabolic pathways

Udriştioiu, A., & Cojocaru, M. (2019) · African Journal of Biological Sciences · doi:10.33472/afjbs.1.3.2019.1-13

Casting iron into the cell fate mold

Kakhlon, O. (2021) · Biochemical Journal · doi:10.1042/bcj20210108 · Cited by 1

Role of VPS34 Complexes in Starvation-Induced Autophagy

Sinha, S. C., Li, Y., Mukhopadhyay, S., Wyatt, S., & Dasanna, S. (2019) · Springer eBooks · doi:10.1007/978-3-319-55387-0_94 · Cited by 1

Pathophysiologische Veränderungen im Alter

Sadjak, A. (2017) · Springer eBooks · doi:10.1007/978-3-662-53101-3_16 · Cited by 1

CORE at the boundary of stress resistance and longevity

Lippi, A., & Kriško, A. (2022) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2022.106277 · Cited by 1

X-rays and metformin cause increased urinary excretion of cell-free nuclear and mitochondrial DNA in aged rats

Gaziev, A. I., Abdullaev, S. A., Minkabirova, G., & Kamenskikh, K. A. (2016) · Journal of Circulating Biomarkers · doi:10.33393/jcb.2016.2068 · Cited by 1

Autophagic activity in the midgut cells of three arachnids responds selectively to different modes of overwintering in caves

Lipovšek, S., Vajs, T., Dariš, B., Novak, T., & Kozel, P. (2024) · PROTOPLASMA · doi:10.1007/s00709-024-02009-x · Cited by 2

Biomolecular conformational changes and transient druggable binding sites through full-length AMPK molecular dynamics simulations

Mendes, G. E. M., Maio, A. R., de Oliveira, G. D. S. R., Rosa, L. C., Costa, L. L., de Oliveira, L. C. V., de Freitas, M. S., Silva, R. C. E., Galvão, R. M. D. S., Coutinho, R. C., et al. (2025) · Journal of Molecular Graphics and Modelling · doi:10.1016/j.jmgm.2025.109039 · Cited by 1

Caloric restriction mimetics: effects of spermidine and berberine on healthy longevity and prevention of aging-associated diseases.

Murillo-Cancho, A. F., Martín‐Latorre, M. D. M., Lozano‐Paniagua, D., & Soriano, B. J. N. (2025) · Nutrición clínica y dietética hospitalaria/Nutrición clínica, dietética hospitalaria · doi:10.12873/451murillo · Cited by 1

A Very-low-energy Fast Involves Increased Adipose Inflammatory Gene Expression: A 6-day Feeding Trial (FASTOMICS-6)

Bråtveit, M., Strømland, P. P., Laupsa‐Borge, J., Skumsnes, L., Dagsland, V. H., Kvistad, S. S., Vogt, E., McCann, A., Thorsen, H. L., Diamantopoulos, A. P., et al. (2025) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/clinem/dgaf570

The study of bone marrow cells in rats according to their age and caloric intake

Kolot, N. (2017) · ScienceRise Biological Science · doi:10.15587/2519-8025.2017.93632 · Cited by 1

Hints for Therapeutic Interventions Through Exploring the Effects of Calorie Restriction on NAFLD by Mechanistic Approach

Hanjani, N. A., & Vafa, M. R. (2018) · Journal of Gastroenterology and Hepatology Research · doi:10.17554/j.issn.2224-3992.2018.07.780 · Cited by 1

“Diet and Exercise Will Help You Live Longer”: The Meme that Turns on Housekeeping Genes

Escobar, K. A., Visconti, L. M., Wallace, A., & VanDusseldorp, T. A. (2019) · Advances in Geriatric Medicine and Research · doi:10.20900/agmr20200002 · Cited by 2

The Importance of Autophagy and Proteostasis in Metabolic Cardiomyopathy

Islas-Carbajal, M. C., Rincón‐Sánchez, A. R., Nava-Valdivia, C. A., & Charles‐Niño, C. (2020) · IntechOpen eBooks · doi:10.5772/intechopen.92727 · Cited by 1

Low Energy Status under Methionine Restriction Is Essentially Independent of Proliferation or Cell Contact Inhibition

Koderer, C., Schmitz, W., Wünsch, A. C., Balint, J., El‐Mesery, M., Volland, J. M., Hartmann, S., Linz, C., Kübler, A. C., & Seher, A. (2022) · Cells · doi:10.3390/cells11030551 · Cited by 1

Overview of Autophagy

Hayat, M. A. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-805421-5.00001-x · Cited by 1

Development of a New Anti-Rabies Antiviral: Effective Treatment with Beclin-1 and Lifespan Prolongation

Parizad, H., Abdoli, A., Mostafavi, E., & Sheikholeslami, F. (2023) · Journal of Biomedical Research & Environmental Sciences · doi:10.37871/jbres1768

Examining Autophagy and Mitophagy as Inducible Mechanisms of Cellular Remodelling

Bloemberg, D. (2017) · UWSpace (University of Waterloo) · Cited by 1

Molecular Mechanisms Underlying Cardiometabolic Disease in Aging

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Caloric Restriction Remodels Energy Metabolic Pathways of Gut Microbiota and Promotes Host AutophagyPreprint

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