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

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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

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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

Insights into the Conserved Regulatory Mechanisms of Human and Yeast Aging

Dahiya, R., Mohammad, T., Alajmi, M. F., Rehman, M. T., Hasan, G. M., Hussain, A., & Hassan, M. I. (2020) · Biomolecules · doi:10.3390/biom10060882 · Cited by 30

The role of lysine acetylation in metabolic sensing and proteostasis

Eftekhari, A., Sabir, U., & Kasumov, T. (2025) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2025.108908 · Cited by 30

Recent insights into the cellular and molecular determinants of aging

Ruan, L., Zhang, X., & Li, R. (2018) · Journal of Cell Science · doi:10.1242/jcs.210831 · Cited by 28

Integrative metabolomics as emerging tool to study autophagy regulation

Stryeck, S., Birner‐Gruenberger, R., & Madl, T. (2017) · Microbial Cell · doi:10.15698/mic2017.08.584 · Cited by 28

Dietary fat composition influences glomerular and proximal convoluted tubule cell structure and autophagic processes in kidneys from calorie-restricted mice

Calvo-Rubio, M., Burón, M. I., López-Lluch, G., Navas, P., de Cabo, R., Ramsey, J. J., Villalba, J. M., & González-Reyes, J. A. (2016) · Aging Cell · doi:10.1111/acel.12451 · Cited by 26

Axin-Mediated Regulation of Lifespan and Muscle Health in C. elegans Requires AMPK-FOXO Signaling

Mallick, A., Ranawade, A., van den Berg, W., & Gupta, B. P. (2020) · iScience · doi:10.1016/j.isci.2020.101843 · Cited by 26

Age-dependent expression changes of circadian system-related genes reveal a potentially conserved link to aging

Barth, E., Srivastava, A., Wengerodt, D., Stojiljkovic, M. R., Axer, H., Witte, O. W., Kretz, A., & Marz, M. (2021) · Aging · doi:10.18632/aging.203788 · Cited by 27

Longevity-modulating effects of symbiosis: insights from Drosophila–Wolbachia interaction

Maistrenko, O. M., Serga, S. V., Vaiserman, A. M., & Kozeretska, I. A. (2016) · Biogerontology · doi:10.1007/s10522-016-9653-9 · Cited by 26

Aging: A cell source limiting factor in tissue engineering

Khorraminejad‐Shirazi, M., Dorvash, M., Estedlal, A., Hoveidaei, A. H., Mazloomrezaei, M., & Mosaddeghi, P. (2019) · World Journal of Stem Cells · doi:10.4252/wjsc.v11.i10.787 · Cited by 28

Leukocyte telomere length in paediatric critical illness: effect of early parenteral nutrition

Verstraete, S., Vanhorebeek, I., van Puffelen, E., Derese, I., Ingels, C., Verbruggen, S. C. A. T., Wouters, P. J., Joosten, K., Hanot, J., Guerra, G. G., et al. (2018) · Critical Care · doi:10.1186/s13054-018-1972-6 · Cited by 25

A systems pharmacology approach to identify the autophagy-inducing effects of Traditional Persian medicinal plants

Mosaddeghi, P., Eslami, M., Farahmandnejad, M., Akhavein, M., Ranjbarfarrokhi, R., Khorraminejad‐Shirazi, M., Shahabinezhad, F., Taghipour, M. J., Dorvash, M., Sakhteman, A., et al. (2021) · Scientific Reports · doi:10.1038/s41598-020-79472-y · Cited by 27

Defects in MAP 1S‐mediated autophagy cause reduction in mouse lifespans especially when fibronectin is overexpressed

Li, W., Zou, J., Yue, F., Song, K., Chen, Q., McKeehan, W. L., Wang, F., Xu, G., Huang, H. W., Yi, J., et al. (2016) · Aging Cell · doi:10.1111/acel.12441 · Cited by 25

Trace lithium in Texas tap water is negatively associated with all-cause mortality and premature death

Fajardo, V. A., LeBlanc, P. J., & Fajardo, V. A. (2017) · Applied Physiology, Nutrition, and Metabolism · doi:10.1139/apnm-2017-0653 · Cited by 25

Amyotrophic lateral sclerosis alters the metabolic aging profile in patient derived fibroblasts

Gerou, M., Hall, B., Woof, R., Allsop, J., Kolb, S. J., Meyer, K., Shaw, P. J., & Allen, S. P. (2021) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2021.04.013 · Cited by 26

Mitochondrial function and nutrient sensing pathways in ageing: enhancing longevity through dietary interventions

Tomtheelnganbee, E., Sah, P., & Sharma, R. (2022) · Biogerontology · doi:10.1007/s10522-022-09978-7 · Cited by 26

Rilmenidine extends lifespan and healthspan in Caenorhabditis elegans via a nischarin I1 ‐imidazoline receptor

Bennett, D., Goyala, A., Statzer, C., Beckett, C. W., Tyshkovskiy, A., Gladyshev, V. N., Ewald, C. Y., & de Magalhães, J. P. (2023) · Aging Cell · doi:10.1111/acel.13774 · Cited by 24

Deletion of Nrip1 Extends Female Mice Longevity, Increases Autophagy, and Delays Cell Senescence

Wang, J., Chen, X., Osland, J. M., Gerber, S. D., Luan, C., Delfino, K. R., Goodwin, L. O., & Yuan, R. (2018) · The Journals of Gerontology Series A · doi:10.1093/gerona/glx257 · Cited by 28

Porcine Circovirus Type 2 ORF5 Protein Induces Autophagy to Promote Viral Replication via the PERK-eIF2α-ATF4 and mTOR-ERK1/2-AMPK Signaling Pathways in PK-15 Cells

Lv, J., Jiang, Y., Feng, Q., Fan, Z., Sun, Y. H., Xu, P., Hou, Y., Zhang, X., Fan, Y., Xu, X., et al. (2020) · Frontiers in Microbiology · doi:10.3389/fmicb.2020.00320 · Cited by 25

Herbal terpenoids activate autophagy and mitophagy through modulation of bioenergetics and protect from metabolic stress, sarcopenia and epigenetic aging

Civiletto, G., Brunetti, D., Lizzo, G., Muller, K., Jacot, G. E., Daskalaki, I., Sizzano, F., Huh, M., Meo, I. D., Colombo, M. N., et al. (2025) · Nature Aging · doi:10.1038/s43587-025-00957-4 · Cited by 24

Tauroursodeoxycholic Acid Attenuates Diet-Induced and Age-Related Peripheral Endoplasmic Reticulum Stress and Cerebral Amyloid Pathology in a Mouse Model of Alzheimer's Disease

Ochiai, T., Nagayama, T., Matsui, K., Amano, K., Sano, T., Wakabayashi, T., & Iwatsubo, T. (2021) · The Journal of Prevention of Alzheimer s Disease · doi:10.14283/jpad.2021.33 · Cited by 23

Methods to Assess Autophagy and Chronological Aging in Yeast

Kainz, K., Tadić, J., Zimmermann, A., Pendl, T., Carmona‐Gutiérrez, D., Ruckenstuhl, C., Eisenberg, T., & Madeo, F. (2016) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/bs.mie.2016.09.086 · Cited by 24

Autophagy: one more Nobel Prize for yeast

Zimmermann, A., Kainz, K., Andryushkova, A., Hofer, S. J., Madeo, F., & Carmona‐Gutiérrez, D. (2016) · Microbial Cell · doi:10.15698/mic2016.12.544 · Cited by 23

Plant Hormone Cytokinins for Modulating Human Aging and Age-Related Diseases

Voller, J., Maková, B., Kadlecová, A., González, G., & Strnad, M. (2017) · Healthy ageing and longevity · doi:10.1007/978-3-319-63001-4_14 · Cited by 23

Toxin-induced hormesis may restrain aging

Lajqi, T., Stojiljkovic, M. R., & Wetzker, R. (2019) · Biogerontology · doi:10.1007/s10522-019-09806-5 · Cited by 22

Long-term treatment with chloroquine increases lifespan in middle-aged male mice possibly via autophagy modulation, proteasome inhibition and glycogen metabolism

Doeppner, T. R., Coman, C., Burdusel, D., Ancuța, D.-L., Brockmeier, U., Pirici, D. N., Kuang, Y., Hermann, D. M., & Popa‐Wagner, A. (2022) · Aging · doi:10.18632/aging.204069 · Cited by 22

Rapamycin modulation of p70 S6 kinase signaling inhibits Rift Valley fever virus pathogenesis

Bell, T. M., Espina, V. A., Senina, S., Lehman, C. W., Brahms, A., Carey, B. D., Lin, S., Lundberg, L., Pinkham, C., Baer, A., et al. (2017) · Antiviral Research · doi:10.1016/j.antiviral.2017.04.011 · Cited by 22

Caloric Restriction Dramatically Stalls Lesion Growth in Mice With Induced Endometriosis

Yin, B., Liu, X., & Guo, S. (2018) · Reproductive Sciences · doi:10.1177/1933719118756755 · Cited by 22

Obesity, Metabolism, and Aging: A Multiscalar Approach

Bentley, R. A., Ross, C. N., & O’Brien, M. J. (2018) · Progress in molecular biology and translational science · doi:10.1016/bs.pmbts.2017.11.016 · Cited by 22

Linking cellular proteostasis to yeast longevity

Sampaio‐Marques, B., & Ludovico, P. (2018) · FEMS Yeast Research · doi:10.1093/femsyr/foy043 · Cited by 23

Tyrosinase-Treated Hydroxytyrosol-Enriched Olive Vegetation Waste with Increased Antioxidant Activity Promotes Autophagy and Inhibits the Inflammatory Response in Human THP-1 Monocytes

Meschini, R., D’Eliseo, D., Filippi, S., Bertini, L., Bizzarri, B. M., Botta, L., Saladino, R., & Velotti, F. (2018) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.8b03630 · Cited by 22

Recent progress regarding the role of autophagy in cardiac disease

Maejima, Y., Titus, A. S., Zablocki, D., & Sadoshima, J. (2025) · Cardiovascular Research · doi:10.1093/cvr/cvaf203 · Cited by 22

Autophagy takes it all – autophagy inducers target immune aging

Zinecker, H., & Simon, A. K. (2022) · Disease Models & Mechanisms · doi:10.1242/dmm.049345 · Cited by 22

Abamectin induces mortality, inhibits food consumption, and causes histological changes in the midgut of the velvetbean caterpillar Anticarsia gemmatalis (Lepidoptera: Noctuidae)

Lima, B. S. A., Rocha, F. A. D., Plata‐Rueda, A., Zanuncio, J. C., Cossolin, J. F. S., Martínez, L. C., & Serrão, J. É. (2023) · Journal of Pest Science · doi:10.1007/s10340-023-01642-4 · Cited by 21

Towards Healthy Longevity: Comprehensive Insights from Molecular Targets and Biomarkers to Biological Clocks

Yusri, K., Kumar, S., Fong, S., Gruber, J., & Sorrentino, V. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25126793 · Cited by 23

Exploring the effects of the acaricide cyflumetofen on the vital organs of the honey bee Apis mellifera (Hymenoptera: Apidae) workers

Reis, A. B., de Oliveira, M. S., Souza, D. D. S., Gomes, D. S., da Silva, L. L., Martínez, L. C., & Serrão, J. É. (2024) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2024.172640 · Cited by 20

Citri Reticulatae Semen Extract Promotes Healthy Aging and Neuroprotection via Autophagy Induction in Caenorhabditis elegans

Long, T., Tang, Y., He, Y.-N., He, C., Chen, X., Guo, M., Wu, J., Yu, L., Yu, C., Law, B. Y. K., et al. (2022) · The Journals of Gerontology Series A · doi:10.1093/gerona/glac136 · Cited by 21

The impact of autophagy on the development of senescence in primary tubular epithelial cells

Baisantry, A., Bhayana, S., Wrede, C., Hegermann, J., Haller, H. G., Melk, A., & Schmitt, R. (2016) · Cell Cycle · doi:10.1080/15384101.2016.1234547 · Cited by 22

Lipotoxicity, Nutrient-Sensing Signals, and Autophagy in Diabetic Nephropathy

Kume, S., & Maegawa, H. (2020) · JMA Journal · doi:10.31662/jmaj.2020-0005 · Cited by 20

Cardiovascular aging: the mitochondrial influence

Sagar, S., & Gustafsson, Å. B. (2023) · The Journal of Cardiovascular Aging · doi:10.20517/jca.2023.22 · Cited by 18

Fasting and calorie restriction modulate age‐associated immunosenescence and inflammaging

Tizazu, A. M. (2024) · Aging Medicine · doi:10.1002/agm2.12342 · Cited by 19

Drosophila Lipase 3 Mediates the Metabolic Response to Starvation and Aging

Hänschke, L., Heier, C., Palacios, S. J. M., Özek, H. E., Thiele, C., Bauer, R., Kühnlein, R. P., & Bülow, M. H. (2022) · Frontiers in Aging · doi:10.3389/fragi.2022.800153 · Cited by 17

Β-blockers activate autophagy on infantile hemangioma-derived endothelial cells in vitro

Lorusso, B., Cerasoli, G., Falco, A., Frati, C., Graiani, G., Madeddu, D., Nogara, A. M., Corradini, E., Roti, G., Cerretani, E., et al. (2022) · Vascular Pharmacology · doi:10.1016/j.vph.2022.107110 · Cited by 20

Aryl hydrocarbon receptor: Linking environment to aging process in elderly patients with asthma

Yang, T., Wan, R., Tu, W., Avvaru, S. N., & Gao, P. (2024) · Chinese Medical Journal · doi:10.1097/cm9.0000000000002960 · Cited by 18

Lithocholic Acid Improves the Survival of Drosophila Melanogaster

Staats, S., Rimbach, G. H., Künstner, A., Graspeuntner, S., Rupp, J., Busch, H. S., Sina, C., Ipharraguerre, I. R., & Wagner, A. E. (2018) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201800424 · Cited by 19

Blood autophagy defect causes accelerated non-hematopoietic organ aging

Fang, Y., Zhu, L., An, N. A., Jiang, G., Qian, J., Zhao, R., Yuan, N., Zhang, S., & Wang, J. (2019) · Aging · doi:10.18632/aging.102086 · Cited by 17

Sargahydroquinoic acid (SHQA) suppresses cellular senescence through Akt/mTOR signaling pathway

Cao, L., Lee, S. G., Park, S., & Kim, H. (2021) · Experimental Gerontology · doi:10.1016/j.exger.2021.111406 · Cited by 17

Branching Off: New Insight Into Lysosomes as Tubular Organelles

Bohnert, K. A., & Johnson, A. E. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.863922 · Cited by 17

Caloric restriction rescues yeast cells from alpha-synuclein toxicity through autophagic control of proteostasis

Sampaio-Marques, B., Pereira, H., Santos, A. R., Teixeira, A., & Ludovico, P. (2018) · Aging · doi:10.18632/aging.101675 · Cited by 14

The role of autophagy in abdominal aortic aneurysm: protective but dysfunctional

Wang, L., Liu, S., Pan, B., Cai, H., Zhou, H., Yang, P., & Wang, W. (2020) · Cell Cycle · doi:10.1080/15384101.2020.1823731 · Cited by 17

Autophagy response to acute high-intensity interval training and moderate-intensity continuous training is dissimilar in skeletal muscle and peripheral blood mononuclear cells and is influenced by sex

Escobar, K. A., Welch, A. M., Wells, A. D., Fennel, Z. J., Nava, R. C., Li, Z., Moriarty, T. A., Nitta, C. H., Zuhl, M., VanDusseldorp, T. A., et al. (2020) · Human Nutrition & Metabolism · doi:10.1016/j.hnm.2020.200118 · Cited by 17

The Impact of Melatonin Supplementation and NLRP3 Inflammasome Deletion on Age-Accompanied Cardiac Damage

Sayed, R. K. A., Fernández‐Ortiz, M., Rahim, I., Fernández‐Martínez, J., Aranda‐Martínez, P., Rusanova, I., Martínez-Ruiz, L., Alsaadawy, R. M., Escames, G., & Acuña-Castroviejo, D. (2021) · Antioxidants · doi:10.3390/antiox10081269 · Cited by 17

Bulk autophagy induction and life extension is achieved when iron is the only limited nutrient in Saccharomyces cerevisiae

Montellà-Manuel, S., Pujol‐Carrion, N., Mechoud, M. A., & de la Torre-Ruiz, M. Á. (2021) · Biochemical Journal · doi:10.1042/bcj20200849 · Cited by 18

The protective effects of angelica organic acid against ox-LDL-induced autophagy dysfunction of HUVECs

Li, X., Zhou, J., Dou, Y., Shi, Y., Wang, Y., Hong, J., Zhao, J., Zhang, J., Yang, Y., Zhou, M., et al. (2020) · BMC Complementary Medicine and Therapies · doi:10.1186/s12906-020-02968-7 · Cited by 15

The biological relevance of pigment epithelium-derived factor on the path from aging to age-related disease

Abooshahab, R., & Dass, C. R. (2021) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2021.111478 · Cited by 15

Generation of somatic mitochondrial DNA-replaced cells for mitochondrial dysfunction treatment

Maeda, H., Kami, D., Maeda, R., Shikuma, A., & Gojo, S. (2021) · Scientific Reports · doi:10.1038/s41598-021-90316-1 · Cited by 16

C. elegans to model autophagy-related human disorders

Wong, S. Q., Kumar, A. V., Mills, J., & Lapierre, L. R. (2020) · Progress in molecular biology and translational science · doi:10.1016/bs.pmbts.2020.01.007 · Cited by 14

Autophagic activity in BC3H1 cells exposed to yessotoxin

Korsnes, M. S., Kolstad, H., Kleiveland, C. R., Korsnes, R., & Ørmen, E. (2015) · Toxicology in Vitro · doi:10.1016/j.tiv.2015.12.010 · Cited by 15

The intracellular metabolome of starving cells

Durand, S., Grajeda‐Iglesias, C., Aprahamian, F., Nirmalathasan, N., Kepp, O., & Kroemer, G. (2021) · Methods in cell biology · doi:10.1016/bs.mcb.2021.04.001 · Cited by 14

Treating Metabolic Dysregulation and Senescence by Caloric Restriction: Killing Two Birds with One Stone?

Russo, L., Babboni, S., Andreassi, M. G., Daher, J., Canale, P., Turco, S. D., & Basta, G. (2025) · Antioxidants · doi:10.3390/antiox14010099 · Cited by 16

Enhancing autophagy by redox regulation extends lifespan in Drosophila

Lennicke, C., Bjedov, I., Grönke, S., Menger, K. E., James, A. M., Castillo-Quan, J. I., van Leeuwen, L. A. G., Foley, A., Buricova, M., Adcott, J., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-60603-w · Cited by 16

Social perception of young adults prolongs the lifespan of aged Drosophila

Cho, L.-C., Yu, C.-C., & Kao, C.-F. (2021) · npj Aging and Mechanisms of Disease · doi:10.1038/s41514-021-00073-8 · Cited by 13

Transcriptome analysis revealed potential mechanisms of differences in physiological stress responses between caged male and female magpies

Wang, Y., Guo, J., Wang, L., Tian, H., & Sui, J. (2019) · BMC Genomics · doi:10.1186/s12864-019-5804-0 · Cited by 14

Shining a light on defective autophagy by proteomics approaches: implications for neurodegenerative illnesses

Domenico, F. D., Zuliani, I., & Tramutola, A. (2019) · Expert Review of Proteomics · doi:10.1080/14789450.2019.1691919 · Cited by 13

Evolutionary analysis of the mTOR pathway provide insights into lifespan extension across mammals

Yang, F. Y., Liu, X., Li, Y., Yu, Z., Huang, X. H., Yang, G. Z., & Xu, S. (2023) · BMC Genomics · doi:10.1186/s12864-023-09554-4 · Cited by 14

C16ORF70/MYTHO promotes healthy aging in C.elegans and prevents cellular senescence in mammals

Franco‐Romero, A., Morbidoni, V., Milan, G., Sartori, R., Wulff, J., Romanello, V., Armani, A., Salviati, L., Conte, M., Salvioli, S., et al. (2024) · Journal of Clinical Investigation · doi:10.1172/jci165814 · Cited by 13

Early-onset dietary restriction maintains mitochondrial health, autophagy and ER function in the left ventricle during aging

Li, S., Lin, Y., Chiang, C.-H., Wang, P., & Chen, C. (2022) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2022.108944 · Cited by 13

Probiotics: The Next Dietary Strategy against Brain Aging

Ong, J.-S., Lew, L.-C., Hor, Y.-Y., & Liong, M. (2022) · Preventive Nutrition and Food Science · doi:10.3746/pnf.2022.27.1.1 · Cited by 13

Cordyceps militaris improves the survival of Dahl salt-sensitive hypertensive rats possibly via influences of mitochondria and autophagy functions

Takakura, K., Ito, S., Sonoda, J., Tabata, K., Shiozaki, M., Nagai, K., Shibata, M., Koike, M., Uchiyama, Y., & Gotow, T. (2017) · Heliyon · doi:10.1016/j.heliyon.2017.e00462 · Cited by 14

The dysregulated autophagy signaling is partially responsible for defective podocyte development in wt1a mutant zebrafish

Zhang, X., Lin, Q., Ren, F., Zhang, J., Dawar, F. U., & Mei, J. (2018) · Aquaculture and Fisheries · doi:10.1016/j.aaf.2018.04.004 · Cited by 13

The Potential Roles of Dec1 and Dec2 in Periodontal Inflammation

Wang, X., Sato, F., Tanimoto, K., Rajeshwaran, N., Thangavelu, L. P., Makishima, M., & BHAWAL, U. K. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms221910349 · Cited by 12

Therapeutic Aspects and Molecular Targets of Autophagy to Control Pancreatic Cancer Management

Rahman, M. A., Ahmed, K. R., Rahman, M. H., Parvez, M. A. K., Lee, I., & Kim, B. (2022) · Biomedicines · doi:10.3390/biomedicines10061459 · Cited by 12

Involvement of Autophagy in Ageing and Chronic Cholestatic Diseases

Pinto, C., Ninfole, E., Benedetti, A., Marzioni, M., & Maroni, L. (2021) · Cells · doi:10.3390/cells10102772 · Cited by 12

Natural Products in Aging: Cellular Mechanisms and Emerging Therapeutics for Age‐Related Disorders

Dixit, V., Chaubey, K. K., Dayal, D., Chole, P. B., Manjunath, B. T., Bachheti, R. K., Gupta, P. C., Bachheti, A., & Worku, L. A. (2025) · Journal of Aging Research · doi:10.1155/jare/6868732 · Cited by 11

Autophagy and longevity: Evolutionary hints from hyper-longevous mammals

Locatelli, A. G., & Cenci, S. (2022) · Frontiers in Endocrinology · doi:10.3389/fendo.2022.1085522 · Cited by 11

Aging-accelerated differential production and aggregation of STAT3 protein in neuronal cells and neural stem cells in the male mouse spinal cord

Zhao, T., Liu, C., Liu, L., Wang, X., & Liu, C. (2022) · Biogerontology · doi:10.1007/s10522-022-10004-z · Cited by 11

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

Caloric restriction reduces the systemic progression of mouse AApoAII amyloidosis

Li, L., Sawashita, J., Ding, X., Yang, M., Xu, Z., Miyahara, H., Mori, M., & Higuchi, K. (2017) · PLoS ONE · doi:10.1371/journal.pone.0172402 · Cited by 12

Embedded-AMP: A Multi-Thread Computational Method for the Systematic Identification of Antimicrobial Peptides Embedded in Proteome Sequences

Carballo, G. M., Vázquez, K. G., García-González, L. A., Río, G. D., & Brizuela, C. A. (2023) · Antibiotics · doi:10.3390/antibiotics12010139 · Cited by 9

Cutting Calories and TXNIP From the Skeletal Muscle to Restore Insulin Sensitivity

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Calorie Restriction Rescues Mitochondrial Dysfunction in Adck2-Deficient Skeletal Muscle

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